Nitromethane by Asch

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Reaxys ID 1698205 View in Reaxys

1/1 CAS Registry Number: 75-52-5 Chemical Name: nitromethane; nitromethae Linear Structure Formula: NO2CH3 Molecular Formula: CH3NO2 Molecular Weight: 61.0403 Type of Substance: acyclic InChI Key: LYGJENNIWJXYER-UHFFFAOYSA-N Note:

Substance Label (101) Label References 2h

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nitromethane

Ferguson, George; Lough, Alan J.; Smith, David M.; Zakaria, Choudhury M.; Glidewell, Christopher; Acta Crystallographica Section C: Crystal Structure Communications; vol. 57; nb. 8; (2001); p. 922 - 923, View in Reaxys; Ihm, Hyejae; Hwang, Soo-Jin; Paek, Kyungsoo; Tetrahedron Letters; vol. 45; nb. 49; (2004); p. 9119 - 9122, View in Reaxys; Peng, Shiyong; Wang, Lei; Wang, Jian; Chemistry - A European Journal; vol. 19; nb. 40; (2013); p. 13322 - 13327, View in Reaxys

Okino, Tomotaka; Nakamura, Satoru; Furukawa, Tomihiro; Takemoto, Yoshiji; Organic Letters; vol. 6; nb. 4; (2004); p. 625 - 627, View in Reaxys; Uraguchi, Daisuke; Sakaki, Sawako; Ooi, Takashi; Journal of the American Chemical Society; vol. 129; nb. 41; (2007); p. 12392 - 12393, View in Reaxys; Zu, Liansuo; Xie, Hexin; Li, Hao; Wang, Jian; Wang, Wei; Advanced Synthesis and Catalysis; vol. 349; nb. 17-18; (2007); p. 2660 - 2664, View in Reaxys; Patent; Mitsui Chemicals, Inc.; National University Corporation Nagoya University; US2009/131716; (2009); (A1) English, View in Reaxys; Dhineshkumar, Jayaraman; Lamani, Manjunath; Alagiri, Kaliyamoorthy; Prabhu, Kandikere Ramaiah; Organic Letters; vol. 15; nb. 5; (2013); p. 1092 - 1095, View in Reaxys; Wang, Hong-Yu; Chai, Zhuo; Zhao, Gang; Tetrahedron; vol. 69; nb. 25; (2013); p. 5104 - 5111, View in Reaxys; Zhang, Lili; Wu, Hao; Yang, Zhongyue; Xu, Xiufang; Zhao, Haitao; Huang, Yaodong; Wang, Yongmei; Tetrahedron; vol. 69; nb. 49; (2013); p. 10644 - 10652, View in Reaxys; Piscopo, Calogero G.; Sartori, Giovanni; Mayoral, Jose A.; Lanari, Daniela; Vaccaro, Luigi; Maggi, Raimondo; Synlett; vol. 24; nb. 19; (2013); p. 2596 - 2600; Art.No: ST-2013-D0688-L, View in Reaxys

Liu, Bin; Li, Xiaofang; Zhang, Jie; Chmielewski, Piotr J.; Organic and Biomolecular Chemistry; vol. 11; nb. 29; (2013); p. 4831 - 4839, View in Reaxys

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Lancianesi, Stefano; Palmieri, Alessandro; Petrini, Marino; Advanced Synthesis and Catalysis; vol. 355; nb. 16; (2013); p. 3285 - 3289, View in Reaxys

Huang, Ling; Zhao, Jianzhang; RSC Advances; vol. 3; nb. 45; (2013); p. 23377 - 23388, View in Reaxys

1a; MeNO&2%

Quintavalla, Arianna; Lanza, Francesco; Montroni, Elisa; Lombardo, Marco; Trombini, Claudio; Journal of Organic Chemistry; vol. 78; nb. 23; (2013); p. 12049 - 12064, View in Reaxys

Jakubec, Pavol; Hawkins, Alison; Felzmann, Wolfgang; Dixon, Darren J.; Journal of the American Chemical Society; vol. 134; nb. 42; (2012); p. 17482 - 17485, View in Reaxys

112a

Patent; Nanyang Technological University; US2011/224429; (2011); (A1) English, View in Reaxys

Table 3,4 Absorbate 6

Roshchina; Shoniya; Lagutova; Fadeev; Russian Journal of Physical Chemistry A; vol. 82; nb. 3; (2008); p. 390 - 396, View in Reaxys

Fioravanti, Stefania; Marchetti, Fabio; Pellacani, Lucio; Ranieri, Luca; Tardella, Paolo A.; Tetrahedron Asymmetry; vol. 19; nb. 2; (2008); p. 231 - 236, View in Reaxys

Ballini, Roberto; Bosica, Giovanna; Parrini, Mauro; Chemistry Letters; nb. 10; (1999); p. 1105 - 1106, View in Reaxys; Meciarova, Maria; Toma, Stefan; Chemistry - A European Journal; vol. 13; nb. 4; (2007); p. 1268 - 1272, View in Reaxys

tab1, entry 10

Al-Shawabkeh, Ali F.; Al-Wahab, Haitham A.; Shahab, Yousif A.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 66; nb. 3; (2007); p. 739 - 744, View in Reaxys

14 (Y = H, Z = NO2)

Zahouily, Mohamed; Mounir, Bahija; Cherki, Hind; Bahlaouan, Bouchaib; Rayadh, Ahmed; Sebti, Said; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 182; nb. 6; (2007); p. 1203 - 1217, View in Reaxys

Obika, Shingo; Kono, Hideki; Yasui, Yoshizumi; Yanada, Reiko; Takemoto, Yoshiji; Journal of Organic Chemistry; vol. 72; nb. 12; (2007); p. 4462 - 4468, View in Reaxys

CH&3%NO&2%

Nicolaou; Majumder, Utpal; Roche, Stephane Philippe; Chen, David Y.-K.; Angewandte Chemie - International Edition; vol. 46; nb. 25; (2007); p. 4715 - 4718, View in Reaxys

Dilman; Lyapkalo; Ioffe; Strelenko; Tartakovsky; Synthesis; nb. 10; (1999); p. 1767 - 1775, View in Reaxys; Halland, Nis; Hazell, Rita G.; Jorgensen, Karl Anker; Journal of Organic Chemistry; vol. 67; nb. 24; (2002); p. 8331 - 8338, View in Reaxys; Arcadi, Antonio; Bianchi, Gabriele; Inesi, Achille; Marinelli, Fabio; Rossi, Leucio; Synlett; nb. 7; (2007); p. 1031 - 1036, View in Reaxys

H3C-NO2

Bonge, Hanne Therese; Hansen, Tore; Synlett; nb. 1; (2007); p. 55 - 58, View in Reaxys

ent-11j

Robak, Maryann T.; Trincado, Monica; Ellman, Jonathan A.; Journal of the American Chemical Society; vol. 129; nb. 49; (2007); p. 15110 - 15111, View in Reaxys

CH3NO2

Kawakami; Suzuki; Tetrahedron Letters; vol. 40; nb. 6; (1999); p. 1157 - 1160, View in Reaxys; Janosik, Tomasz; Bergman, Jan; Tetrahedron; vol. 55; nb. 8; (1999); p. 2371 - 2380, View in Reaxys; Bailey; Molinski; Journal of Organic Chemistry; vol. 64; nb. 7; (1999); p. 2500 - 2504, View in Reaxys; Aixill, W. Joanne; Mills, Peter B.; Compton, Richard G.; Prieto, Francisco; Rueda, Manuela; Journal of Physical Chemistry B: Condensed Matter, Materials, Surfaces, Interfaces, & Biophysical Chemistry; vol. 102; nb. 46; (1998); p. 9187 - 9190, View in Reaxys; Bardina; Gas'kov; Kovaleva; Kudryavtseva; Nikitin; Russian Journal of Physical Chemistry A; vol. 73; nb. 1; (1999); p. 101 - 105, View in Reaxys; Pak; Gartman; Yaganova; Neifel'd; Russian Journal of General Chemistry; vol. 68; nb. 12; (1998); p. 1930 - 1934, View in Reaxys; Novellino, Luisa; D'Ischia, Marco; Prota, Giuseppe; Synthesis; nb. 5; (1999); p. 793 - 796, View in Reaxys; Habermann, Joerg; Ley, Steven V.; Scott, James S.; Journal of the Chemical Society - Perkin Transactions 1; nb. 10; (1999); p. 1253 - 1255, View in Reaxys; Silveira, Claudio C.; Bernardi, Carmem R.; Braga, Antonio L.; Kaufman, Teodoro S.; Tetrahedron Letters; vol. 40; nb. 27; (1999); p. 4969 - 4972, View in Reaxys; Lakhvich; Kozinets; Katok; Russian Journal of Organic Chemistry; vol. 34; nb. 7; (1998); p. 989 - 993, View in Reaxys; Corey; Zhang, Fu-Yao; Angewandte Chemie - International Edition; vol. 38; nb. 13-14; (1999); p. 1931 - 1934, View in Reaxys; Showalter, H. D. Hollis; Pohlmann, Gerd; Organic Preparations and Procedures International; vol. 24; nb. 4; (1992); p. 484 - 488, View in Reaxys; Rademann, Joerg; Meldal, Morten; Bock, Klaus; Chemistry - A European Journal; vol. 5; nb. 4; (1999); p. 1218 - 1225, View in Reaxys; Gravestock, David; Peirson, Ian G.; Tetrahedron Letters; vol. 41; nb. 18; (2000); p. 3497 3500, View in Reaxys; Yashiro; Nishida; Kobayashi; Ohno; Synlett; nb. 3; (2000); p. 361 - 362, View in Reaxys; Yamada, Ken-Ichi; Harwood, Simon J.; Groeger, Harald; Shibasaki, Masakatsu; Angewandte Chemie - International Edition; vol. 38; nb. 23; (1999); p. 3504 - 3506, View in Reaxys; Blackburn, G. Michael; Beadham, Ian G.; Adams, Harry; Hutchinson, Alistair P.; Nicklin, Stephen; Journal of the Chemical Society, Perkin Transactions 1; nb. 2; (2000); p. 225 - 230, View in Reaxys; Teng, Yonghong; Yamaguchi, Yoichi; Takemoto, Tetsuya; Dai, Lianxin; Tabata, Kenji; Suzuki, Eiji; Chemical Communications; nb. 5; (2000); p. 371 - 372, View in Reaxys; Williams, David R.; Brugel, Todd A.; Organic Letters; vol. 2; nb. 8; (2000); p. 1023 - 1026, View in Reaxys; Tabata, Kenji; Teng, Yonghong; Yamaguchi, Yoichi; Sakurai, Hiroaki; Suzuki, Eiji; Journal of Physical Chemistry A; vol. 104; nb. 12; (2000); p. 2648 - 2654, View in Reaxys; Wright, Stephen W.; Organic Preparations and Procedures International; vol. 32; nb. 4; (2000); p. 376 - 379, View in Reaxys; Wollenhaupt, Matthias; Crowley, John N.; Journal of Physical Chem-

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istry A; vol. 104; nb. 27; (2000); p. 6429 - 6438, View in Reaxys; Gueyrard; Barillari; Iori; Palmieri; Rollin; Tetrahedron Letters; vol. 41; nb. 43; (2000); p. 8307 - 8309, View in Reaxys; Corey; Zhang, Fu-Yao; Organic Letters; vol. 2; nb. 26; (2000); p. 4257 - 4258, View in Reaxys; Andersen, Rosaleen J.; Ashwell, Susan; Garnett, Ian; Golding, Bernard T.; Journal of the Chemical Society, Perkin Transactions 1; nb. 24; (2000); p. 4488 - 4498, View in Reaxys; Bardina; Kovaleva; Nikitin; Russian Journal of Physical Chemistry A; vol. 75; nb. 3; (2001); p. 442 - 445, View in Reaxys; Gulevskaya; Goryunenko; Pozharskii; Chemistry of Heterocyclic Compounds; vol. 36; nb. 8; (2000); p. 975 - 980, View in Reaxys; Yip; Handerson; Tranmer; Tam; Journal of Organic Chemistry; vol. 66; nb. 1; (2001); p. 276 - 286, View in Reaxys; Easton; Xia; Pitt; Ferrante; Poulos; Rathjen; Synthesis; nb. 3; (2001); p. 451 - 457, View in Reaxys; Rudolph, Joachim; Hannig, Frithjof; Theis, Heidi; Wischnat, Ralf; Organic Letters; vol. 3; nb. 20; (2001); p. 3153 - 3155, View in Reaxys; Tsotinis, Andrew; Panoussopoulou, Maria; Sivananthan, Sachi; Sugden, David; Farmaco; vol. 56; nb. 9; (2001); p. 725 - 729, View in Reaxys; Bojarski, Andrzej J; Mokrosz, Maria J; Minol, Sijka Charakchieva; Koziol, Aneta; Wesolowska, Anna; Tatarczynska, Ewa; Klodzinska, Aleksandra; Chojnacka-Wojcik, Ewa; Bioorganic and Medicinal Chemistry; vol. 10; nb. 1; (2002); p. 87 - 95, View in Reaxys; Shibayama, Satoru; Konno, Tsutomu; Ishihara, Takashi; Yamanaka, Hiroki; Journal of Fluorine Chemistry; vol. 111; nb. 1; (2001); p. 91 - 100, View in Reaxys; Andreu, Inmaculada; Cabedo, Nuria; Atassi, Ghanem; Pierre, Alain; Caignard, Daniel H; Renard, Pierre; Cortes, Diego; Bermejo, Almudena; Tetrahedron Letters; vol. 43; nb. 5; (2002); p. 757 - 759, View in Reaxys; Sosnicki, Jacek G; Westerlich, Slawomir; Tetrahedron Letters; vol. 43; nb. 7; (2002); p. 1325 - 1328, View in Reaxys; Iki, Nobuhiko; Suzuki, Takehiro; Koyama, Katsuyoshi; Kabuto, Chizuko; Miyano, Sotaro; Organic Letters; vol. 4; nb. 4; (2002); p. 509 - 512, View in Reaxys; Inbaraj, J. Johnson; Bilski, Piotr; Chignell, Colin F.; Photochemistry and Photobiology; vol. 75; nb. 2; (2002); p. 107 - 116, View in Reaxys; Ouillon; Pinan-Lucarre; Ranson; Baranovic; Journal of Chemical Physics; vol. 116; nb. 11; (2002); p. 4611 - 4625, View in Reaxys; Muratake, Hideaki; Natsume, Mitsutaka; Tetrahedron Letters; vol. 43; nb. 16; (2002); p. 2913 - 2917, View in Reaxys; Hirakata, Masaki; Yoshimura, Kosaku; Usui, Shuji; Nishimoto, Koji; Fukazawa, Yoshimasa; Tetrahedron Letters; vol. 43; nb. 10; (2002); p. 1859 - 1861, View in Reaxys; Konkel, Jamie T; Fan, Junfa; Jayachandran; Kirk, Kenneth L; Journal of Fluorine Chemistry; vol. 115; nb. 1; (2002); p. 27 - 32, View in Reaxys; Kantlehner, Willi; Haug, Erwin; Stieglitz, Ruediger; Frey, Wolfgang; Kress, Ralf; Mezger, Jochen; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 57; nb. 4; (2002); p. 399 - 419, View in Reaxys; Trost, Barry M.; Yeh, Vince S. C.; Ito, Hisanako; Bremeyer, Nadine; Organic Letters; vol. 4; nb. 16; (2002); p. 2621 - 2623, View in Reaxys; Newkome, George R.; Yoo, Kyung Soo; Moorefield, Charles N.; Chemical Communications; nb. 18; (2002); p. 2164 - 2165, View in Reaxys; Noland, Wayland E.; Kedrowski, Brant L.; Journal of Organic Chemistry; vol. 67; nb. 24; (2002); p. 8366 - 8373, View in Reaxys; Chan, Ally S. Y.; Deiner, L. Jay; Friend; Journal of Physical Chemistry B; vol. 106; nb. 51; (2002); p. 13318 - 13325, View in Reaxys; Velmathi; Swarnalakshmi; Narasimhan; Tetrahedron Asymmetry; vol. 14; nb. 1; (2003); p. 113 - 117, View in Reaxys; Tsotinis, Andrew; Eleutheriades, Andreas; Hough, Katherine; Sugden, David; Chemical communications (Cambridge, England); nb. 3; (2003); p. 382 - 383, View in Reaxys; Kusurkar, Radhika S.; Goswami, Shailesh K.; Vyas, Sandhya M.; Tetrahedron Letters; vol. 44; nb. 25; (2003); p. 4761 - 4763, View in Reaxys; Rivas, Lucrecia; Quintero, Leticia; Fourrey, Jean-Louis; Benhida, Rachid; Tetrahedron Letters; vol. 43; nb. 42; (2002); p. 7639 - 7641, View in Reaxys; Sanki, Aditya K; Suresh, Cheravakkattu G; Falgune, Usha D; Pathak, Tanmaya; Organic letters; vol. 5; nb. 8; (2003); p. 1285 1288, View in Reaxys; Jang, Yeong-Jiunn; Shih, Yuh-Kuo; Liu, Jing-Yuan; Kuo, Wen-Yu; Yao, Ching-Fa; Chemistry - A European Journal; vol. 9; nb. 9; (2003); p. 2123 - 2128, View in Reaxys; Hart, David J.; Patterson, Suzanne; Unch, James P.; Synlett; nb. 9 SPEC. ISS.; (2003); p. 1334 - 1338, View in Reaxys; Miyake, Noriaki; Kitazume, Tomoya; Journal of Fluorine Chemistry; vol. 122; nb. 2; (2003); p. 243 - 246, View in Reaxys; Gong, Yuefa; Kato, Katsuya; Journal of Fluorine Chemistry; vol. 121; nb. 2; (2003); p. 141 - 146, View in Reaxys; Krishnaswamy, Devanathan; Govande, Vidyesh V.; Deshmukh, Abdul Rakeeb A. S.; Synthesis; nb. 12; (2003); p. 1903 - 1908, View in Reaxys; Atkinson, Sov; Meredith, Paul; Synlett; nb. 12; (2003); p. 1853 - 1855, View in Reaxys; Searcey, Mark; Grewal, Sukhwant S.; Madeo, Fiorenza; Tsoungas, Petros G.; Tetrahedron Letters; vol. 44; nb. 35; (2003); p. 6745 - 6747, View in Reaxys; Gao, Jian; Martell; Organic and Biomolecular Chemistry; vol. 1; nb. 15; (2003); p. 2801 - 2806, View in Reaxys; Jiao; DeJoseph Jr.; Garscadden; Journal of Physical Chemistry A; vol. 107; nb. 42; (2003); p. 9040 - 9044, View in Reaxys; Liu, Hong-Min; Zhang, Fuyi; Zou, Da-Peng; Chemical Communications; nb. 16; (2003); p. 2044 - 2045, View in Reaxys; Ying, Laiqiang; Gervay-Hague, Jacquelyn; Carbohydrate Research; vol. 339; nb. 2; (2004); p. 367 - 375, View in Reaxys; Ishikawa, Teruhiko; Shimizu, Yoshihiro; Kudoh, Takayuki; Saito, Seiki; Organic Letters; vol. 5; nb. 21; (2003); p. 3879 - 3882, View in Reaxys; Foresti, Elisabetta; Palmieri, Gianni; Petrini, Marino; Profeta, Roberto; Organic and Biomolecular Chemistry; vol. 1; nb. 23; (2003); p. 4275 - 4281, View in Reaxys; Hallinan, E. Ann; Kramer, Steven W.; Houdek, Stephen C.; Moore, William M.; Jerome, Gina M.; Spangler, Dale P.; Stevens, Anna M.; Shieh, Huey S.; Manning, Pamela T.; Pitzele, Barnett S.; Organic and Biomolecular Chemistry; vol. 1; nb. 20; (2003); p. 3527 - 3534, View in Reaxys; Hammond, David M.; Edmont, Dolores; Hornillo-Araujo, Ana R.; Williams, David M.; Organic and Biomolecular Chemistry; vol. 1; nb. 23; (2003); p. 4166 - 4172, View in Reaxys; Dominguez, Rosa Maria; Herize, Armando; Rotinov, Alexandra; Alvarez-Aular, Alvaro; Visbal, Gonzalo; Chuchani, Gabriel; Journal of Physical Organic Chemistry; vol. 17; nb. 5; (2004); p. 399 - 408, View in Reaxys; Demont, Emmanuel; Eatherton, Andrew; Frampton, Christopher S.; Kahn, Irfan; Redshaw, Sally; Synlett; nb. 4; (2004); p. 684 - 687, View in Reaxys; Moreau, Anne; Couture, Axel; Deniau, Eric; Grandclaudon, Pierre; Lebrun, Stephane; Tetrahedron; vol. 60; nb. 29; (2004); p. 6169 - 6176, View in Reaxys; Felluga, Fulvia; Gombac, Valentina; Pitacco, Giuliana; Valentin, Ennio; Tetrahedron Asymmetry; vol. 15; nb. 20; (2004); p. 3323 - 3327, View in Reaxys; Ballini, Roberto; Balsamini, Cesare; Bartoccini, Francesca; Gianotti, Massimo; Martinelli, Chiara; Savoretti, Nicoletta; Synthesis; nb. 2; (2005); p. 296 - 300; Art.No:

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Z16604SS, View in Reaxys; Chetia, Apurba; Longchar, Moanochet; Lekhok, Kushal C.; Boruah, Romesh C.; Synlett; nb. 7; (2004); p. 1309 - 1311, View in Reaxys; Palombi, Laura; Feroci, Marta; Orsini, Monica; Inesi, Achille; Chemical Communications; nb. 16; (2004); p. 1846 - 1847, View in Reaxys; Lee, Anna; Kim, Woosung; Lee, Jinwoo; Hyeon, Taeghwan; Kim, B. Moon; Tetrahedron Asymmetry; vol. 15; nb. 17; (2004); p. 2595 - 2598, View in Reaxys; Gao, Feifeng; Deng, Minzhi; Qian, Changtao; Tetrahedron; vol. 61; nb. 52; (2005); p. 12238 - 12243, View in Reaxys; Buchanan, David J.; Dixon, Darren J.; Looker, Brian E.; Synlett; nb. 12; (2005); p. 1948 - 1950; Art.No: D12405ST, View in Reaxys; Abello; Medina; Tichit; Perez-Ramirez; Cesteros; Salagre; Sueiras; Chemical Communications; nb. 11; (2005); p. 1453 - 1455, View in Reaxys; Storz, Thomas; Vangrevelinghe, Eric; Dittmar, Peter; Synthesis; nb. 15; (2005); p. 2562 2570; Art.No: M01105SS, View in Reaxys; Allmendinger, Lars; Bauschke, Gerd; Paintner, Franz F.; Synlett; nb. 17; (2005); p. 2615 - 2618; Art.No: D24805ST, View in Reaxys; Sohtome, Yoshihiro; Takemura, Nobuko; Iguchi, Toshitsugu; Hashimoto, Yuichi; Nagasawa, Kazuo; Synlett; nb. 1; (2006); p. 144 - 146; Art.No: Y07305ST, View in Reaxys; Palmer, Francine N.; Lach, Franck; Poriel, Cyril; Pepper, Adrian G.; Bagley, Mark C.; Slawin, Alexandra M. Z.; Moody, Christopher J.; Organic and Biomolecular Chemistry; vol. 3; nb. 20; (2005); p. 3805 - 3811, View in Reaxys; Kovaleva; Lanin; Samadani Langerudi; Russian Journal of Physical Chemistry A; vol. 80; nb. 6; (2006); p. 945 - 949, View in Reaxys; Shimizu, Kazuya; Takimoto, Masanori; Sato, Yoshihiro; Mori, Miwako; Journal of Organometallic Chemistry; vol. 691; nb. 24-25; (2006); p. 5466 - 5475, View in Reaxys; Uozumi, Yasuhiro; Suzuka, Toshimasa; Journal of Organic Chemistry; vol. 71; nb. 22; (2006); p. 8644 - 8646, View in Reaxys; Gan, Changsheng; Chen, Xing; Lai, Guoyin; Wang, Zhiyong; Synlett; nb. 3; (2006); p. 387 - 390, View in Reaxys; O'Leary, Jane; Formosa, Xavier; Skranc, Wolfgang; Wallis, John D.; Organic and Biomolecular Chemistry; vol. 3; nb. 18; (2005); p. 3273 - 3283, View in Reaxys; Pedras, M. Soledade C.; Suchy, Mojmir; Ahiahonu, Pearson W. K.; Organic and Biomolecular Chemistry; vol. 4; nb. 4; (2006); p. 691 - 701, View in Reaxys; Riehn; Kunitski; Matylitsky; Gelin; Brutschy; Physical Chemistry Chemical Physics; vol. 7; nb. 23; (2005); p. 3955 - 3962, View in Reaxys; Mitchell, Claire E. T.; Brenner, Stacey E.; Garcia-Fortanet, Jorge; Ley, Steven V.; Organic and Biomolecular Chemistry; vol. 4; nb. 10; (2006); p. 2039 - 2049, View in Reaxys; Wang, Jian; Li, Hao; Lou, Bihshow; Zu, Liansuo; Guo, Hua; Wang, Wei; Chemistry - A European Journal; vol. 12; nb. 16; (2006); p. 4321 - 4332, View in Reaxys; Mansawat, Woraluk; Saengswang, Ittiphol; U-prasitwong, Palita; Bhanthumnavin, Worawan; Vilaivan, Tirayut; Tetrahedron Letters; vol. 48; nb. 24; (2007); p. 4235 - 4238, View in Reaxys; Molteni, Marco; Consonni, Roberto; Giovenzana, Tommaso; Malpezzi, Luciana; Zanda, Matteo; Journal of Fluorine Chemistry; vol. 127; nb. 7; (2006); p. 901 - 908, View in Reaxys; Hemeon, Ivan; Bennet, Andrew J.; Organic and Biomolecular Chemistry; vol. 4; nb. 15; (2006); p. 2986 - 2992, View in Reaxys; Tuan, Dang Thanh; Tung, Dang Thanh; Langer, Peter; Synlett; nb. 17; (2006); p. 2812 2814, View in Reaxys; Wada, Yasuhiro; Nishida, Naoto; Kurono, Nobuhito; Ohkuma, Takashi; Orito, Kazuhiko; European Journal of Organic Chemistry; nb. 26; (2007); p. 4320 - 4327, View in Reaxys; Kim, HanJe; Lindsey, Jonathan S.; Journal of Organic Chemistry; vol. 70; nb. 14; (2005); p. 5475 - 5486, View in Reaxys; Mahasneh, Ali S.; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 61; nb. 9; (2006); p. 1162 - 1165, View in Reaxys; Ginotra, Sandeep K.; Singh, Vinod K.; Organic and Biomolecular Chemistry; vol. 5; nb. 24; (2007); p. 3932 - 3937, View in Reaxys; Pandya, Shashi U.; Dickins, Rachel S.; Parker, David; Organic and Biomolecular Chemistry; vol. 5; nb. 23; (2007); p. 3842 - 3846, View in Reaxys educt to 2

Wang, Dao-Lin; Imafuku, Kimiaki; Heterocycles; vol. 62; (2004); p. 667 - 677, View in Reaxys; Liu, FengWu; Yan, Lin; Zhang, Jing-Yu; Liu, Hong-Min; Carbohydrate Research; vol. 341; nb. 3; (2006); p. 332 338, View in Reaxys

2a-H

Thanh, Binh Phan; Mayr, Herbert; European Journal of Organic Chemistry; nb. 11; (2006); p. 2530 - 2537, View in Reaxys

11a

Ye, Weiping; Leow, Dasheng; Goh, Serena Li Min; Tan, Chin-Tong; Chian, Chee-Hoe; Tan, ChoonHong; Tetrahedron Letters; vol. 47; nb. 6; (2006); p. 1007 - 1010, View in Reaxys

8, Tab. 4

Kantam, M. Lakshmi; Ravindra; Reddy, Ch. Venkat; Sreedhar; Choudary; Advanced Synthesis and Catalysis; vol. 348; nb. 4-5; (2006); p. 569 - 578, View in Reaxys

educt to 3

Nemoto, Tetsuhiro; Jin, Long; Nakamura, Hiroshi; Hamada, Yasumasa; Tetrahedron Letters; vol. 47; nb. 37; (2006); p. 6577 - 6581, View in Reaxys

Table 1, run 19

Novikov; Abaidullina; Gainutdinova; Varfalomeev; Solomonov; Russian Journal of Physical Chemistry A; vol. 80; nb. 11; (2006); p. 1790 - 1794, View in Reaxys

Compound 5; 5

Patent; Japan Science and Technology Agency; National University Corporation Kagoshima University; EP1726596; (2006); (A1) English, View in Reaxys

Tab. 1, entry 5

Veldurthy, Bhaskar; Clacens, Jean Marc; Figueras, Francois; Advanced Synthesis and Catalysis; vol. 347; nb. 6; (2005); p. 767 - 771, View in Reaxys

NME-h3

Makowska, Anna; Szydlowski, Jerzy; Journal of Chemical and Engineering Data; vol. 50; nb. 4; (2005); p. 1365 - 1369, View in Reaxys

educt to 6

Li, Donghong; Zhang, Yongbin; Guo, Wei; Xia, Chizhong; Heterocycles; vol. 65; nb. 5; (2005); p. 1063 1069, View in Reaxys

13/412

2016-04-19 03:35:30

Tab 1/19

Onuchak; Lapshin; Kudryashov; Akopova; Russian Journal of Physical Chemistry A; vol. 79; nb. 5; (2005); p. 817 - 819, View in Reaxys

7, R1=R2=H

Kawai, Kouichi; Ebata, Takuma; Kitazume, Tomoya; Journal of Fluorine Chemistry; vol. 126; nb. 6; (2005); p. 956 - 961, View in Reaxys

NME

Szydlowski; Milewska; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 505 - 508, View in Reaxys; Milewska; Siporska; Szydlowski; Polish Journal of Chemistry; vol. 78; nb. 4; (2004); p. 591 - 594, View in Reaxys

Ooi, Takashi; Fujioka, Shingo; Maruoka, Keiji; Journal of the American Chemical Society; vol. 126; nb. 38; (2004); p. 11790 - 11791, View in Reaxys

1a-H

Bug, Thorsten; Lemek, Tadeusz; Mayr, Herbert; Journal of Organic Chemistry; vol. 69; nb. 22; (2004); p. 7565 - 7576, View in Reaxys

Chanda, Kaushik; Dutta, Milan Ch.; Karim; Vishwakarma; Journal of the Indian Chemical Society; vol. 81; nb. 9; (2004); p. 791 - 793, View in Reaxys

CH3-NO2

El Blidi, Lahssen; Crestia, Dominique; Gallienne, Estelle; Demuynck, Colette; Bolte, Jean; Lemaire, Marielle; Tetrahedron Asymmetry; vol. 15; nb. 18; (2004); p. 2951 - 2954, View in Reaxys

2c,2d

Ghosh, Tarun; Bandyopadhyay, Chandrakanta; Tetrahedron Letters; vol. 45; nb. 32; (2004); p. 6169 6172, View in Reaxys

1, R=H

Youn, So Won; Kim, Yong Hae; Synlett; nb. 6; (2000); p. 880 - 882, View in Reaxys; Ballini, Roberto; Bosica, Giovanna; Livi, Damiana; Palmieri, Alessandro; Maggi, Raimondo; Sartori, Giovanni; Tetrahedron Letters; vol. 44; nb. 11; (2003); p. 2271 - 2273, View in Reaxys

educt to 12

Larionov, Oleg V.; Savel'eva, Tatyana F.; Kochetkov, Konstantin A.; Ikonnokov, Nikolai S.; Kozhushkov, Sergei I.; Yufit, Dmitrii S.; Howard, Judith A. K.; Khrustalev, Viktor N.; Belokon, Yuri N.; De Meijere, Armin; European Journal of Organic Chemistry; nb. 5; (2003); p. 869 - 877, View in Reaxys

Kunetsky, Roman A.; Dilman, Alexander D.; Tsvaygboym, Konstantin P.; Ioffe, Sema L.; Strelenko, Yury A.; Tartakovsky, Vladimir A.; Synthesis; nb. 9; (2003); p. 1339 - 1346, View in Reaxys

educt to 7

Chen, Bang-Chi; Chao, Sam T.; Sundeen, Joseph E.; Tellew, John; Ahmad, Saleem; Tetrahedron Letters; vol. 43; nb. 9; (2002); p. 1595 - 1596, View in Reaxys

R3CH2NO2, R3=H

Pathak, Rashmi; Shaw, Arun K.; Bhaduri, Amiya P.; Chandrasekhar; Srivastava, Anil; Srivastava, Kishore K.; Chaturvedi, Vineeta; Srivastava, Ranjana; Srivastava, Brahm S.; Arora, Shalini; Sinha, Sudhir; Bioorganic and Medicinal Chemistry; vol. 10; nb. 6; (2002); p. 1695 - 1702, View in Reaxys

Liu, Tianjun; Schneider, Hans-Joerg; Angewandte Chemie - International Edition; vol. 41; nb. 8; (2002); p. 1368 - 1370, View in Reaxys

educt to reactions Ma, Dawei; Pan, Qiangbiao; Han, Fushe; Tetrahedron Letters; vol. 43; nb. 51; (2002); p. 9401 - 9403, View in Reaxys 8a

Kisanga, Philip B.; Ilankumaran, Palanichamy; Fetterly, Brandon M.; Verkade, John G.; Journal of Organic Chemistry; vol. 67; nb. 11; (2002); p. 3555 - 3560, View in Reaxys

2, R=H

Demicheli, Giuseppina; Maggi, Raimondo; Mazzacani, Alessandro; Righi, Paolo; Sartori, Giovanni; Bigi, Franca; Tetrahedron Letters; vol. 42; nb. 12; (2001); p. 2401 - 2403, View in Reaxys

educt to X

Pashkovskii; Lakhvich; Koval'skaya; Kozlov; Russian Journal of Organic Chemistry; vol. 37; nb. 3; (2001); p. 375 - 381, View in Reaxys

1, R=Me

Kidwai; Sapra; Organic Preparations and Procedures International; vol. 33; nb. 4; (2001); p. 381 - 386, View in Reaxys

Scheme 1

Wadsworth, Alan H.; Newman, John J.; Wipperman, Mark D.; Fellows, Ian; Sutherland, Derek R.; Journal of Labelled Compounds and Radiopharmaceuticals; vol. 43; nb. 1; (2000); p. 11 - 28, View in Reaxys

Table 2, entry 26

Bardina; Kovaleva; Nikitin; Russian Journal of Physical Chemistry A; vol. 74; nb. 3; (2000); p. 421 - 425, View in Reaxys

Ballini, Roberto; Bigi, Franca; Gogni, Elena; Maggi, Raimondo; Sartori, Giovanni; Journal of Catalysis; vol. 191; nb. 2; (2000); p. 348 - 353, View in Reaxys

Makarevich; Afanas'ev; Telysheva; Monakov; Russian Journal of Physical Chemistry A; vol. 74; nb. 12; (2000); p. 2001 - 2007, View in Reaxys

CH3NO

Kisanga, Philip B.; Verkade, John G.; Journal of Organic Chemistry; vol. 64; nb. 12; (1999); p. 4298 - 4303, View in Reaxys

Castro, Francisco J. Freire; Vila, Manuel M.; Jenkins, Paul R.; Sharma, Madan L.; Tustin, Gary; et al.; Synlett; nb. 6; (1999); p. 798 - 800, View in Reaxys

14/412

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educt to 7a-f

Lucet, Denis; Sabelle, Stephane; Kostelitz, Olivier; Le Gall, Thierry; Mioskowski, Charles; European Journal of Organic Chemistry; nb. 10; (1999); p. 2583 - 2591, View in Reaxys

Scheme 2/b

Taylor, Edward C.; Liu, Bin; Tetrahedron Letters; vol. 40; nb. 21; (1999); p. 4023 - 4026, View in Reaxys

1, R1=R2=H

Sebti, Said; Boukhal, Hassan; Hanafi, Naima; Boulaajaj, Said; Tetrahedron Letters; vol. 40; nb. 34; (1999); p. 6207 - 6209, View in Reaxys

Verbitskii; Slabko; Kaminskii; Russian Journal of Organic Chemistry; vol. 34; nb. 9; (1998); p. 1343 - 1347, View in Reaxys

Arai, Noriyoshi; Narasaka, Koichi; Bulletin of the Chemical Society of Japan; vol. 70; nb. 10; (1997); p. 2525 - 2534, View in Reaxys

Patent-Specific Data (8) Prophetic ComLocation in Patent References pound Page/Page column

Patent; NOVARTIS AG; Bock, Mark Gary; Gaul, Christoph; Gummadi, Venkateshwar Rao; Moebitz, Henrik; Sengupta, Saumitra; US2014/45872; (2014); (A1) English, View in Reaxys; Patent; BOEHRINGER INGELHEIM INTERNATIONAL GMBH; BRENNEMAN, Jehrod Burnett; GINN, John; LOWE, Michael D.; SARKO, Christopher Ronald; TASBER, Edward S.; ZHANG, Zhonghua; US2014/73629; (2014); (A1) English, View in Reaxys Patent; THE BOARD OF REGENTS OF THE NEVADA SYSTEM OF HIGHER EDUCATION on behalf of THE UNIVERSITY OF; ZHANG, Hui; WO2014/194280; (2014); (A2) English, View in Reaxys Patent; Trauth, Daniel M.; Green, George D.; Swedo, Raymond J.; US2011/92750; (2011); (A1) English, View in Reaxys Patent; UNIBAN - Universidade Bandeirante de Sao Paulo - Academia Paulista Anchieta S/C LTDA; FAPESP - Fundacao de Amparo a Pesquisa do Estado de Sao Paulo; WO2008/3155; (2008); (A2) English, View in Reaxys Patent; Bromine Compounds Ltd.; US2007/249501; (2007); (A1) English, View in Reaxys Patent; Mitsui Chemicals, Inc.; US2005/215832; (2005); (A1) English, View in Reaxys Patent; BAYER CROPSCIENCE AG; WO2004/96772; (2004); (A1) English, View in Reaxys

prophetic product

Patent; Nippon Shokubai Co., Ltd.; EP1205462; (2002); (A1) English, View in Reaxys

Related Structure (4) Related Structure Referenced Com- References pound The tautomers given are discussed.

formohydroxamic acid

Tran, Sophia D.; Tronic, Tristan A.; Kaminsky, Werner; Michael Heinekey; Mayer, James M.; Inorganica Chimica Acta; vol. 369; nb. 1; (2011); p. 126 - 132, View in Reaxys

The following tau- formohydroxamic tomers are disacid cussed: /BRN= 1847516/

Veltwisch, Dieter; Asmus, Klaus-Dieter; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1982); p. 1143 - 1146, View in Reaxys; Bilski, Piotr; Reszka, Krzysztof; Chignell, Colin F.; Journal of the American Chemical Society; vol. 116; nb. 22; (1994); p. 9883 - 9889, View in Reaxys Pivina et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 24; (1975); p. 59,60,61; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 24; (1975); p. 68, View in Reaxys; Dakhis et al.; Journal of Molecular Structure; vol. 14; (1972); p. 321,322, View in Reaxys; Cox; Waring; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 68; (1972); p. 1060, View in Reaxys

Zur Existenz einer aci-Form. Derivative (71) Comment (Derivative) By formation of salt/complex with hexane. Addition-

Walden; Birr; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 163; (1933); p. 273,335, View in Reaxys Derivative

References Kamlet, Mortimer J.; Carr, Peter W.; Taft, R. W.; Abraham, Michael H.; Journal of the American Chemical Society; vol. 103; nb. 20; (1981); p. 6062 - 6066, View in Reaxys

15/412

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al data: free energie By formation of salt/complex with cyclohexane. Additional data: free energie

Kamlet, Mortimer J.; Carr, Peter W.; Taft, R. W.; Abraham, Michael H.; Journal of the American Chemical Society; vol. 103; nb. 20; (1981); p. 6062 - 6066, View in Reaxys

By formation of salt/complex with triethylamine. Additional data: free energie

Kamlet, Mortimer J.; Carr, Peter W.; Taft, R. W.; Abraham, Michael H.; Journal of the American Chemical Society; vol. 103; nb. 20; (1981); p. 6062 - 6066, View in Reaxys

By formation of salt/complex with diethyl ether. Additional data: free energie

Kamlet, Mortimer J.; Carr, Peter W.; Taft, R. W.; Abraham, Michael H.; Journal of the American Chemical Society; vol. 103; nb. 20; (1981); p. 6062 - 6066, View in Reaxys

By formation of salt/complex with ethyl acetate. Additional data: free energie

Kamlet, Mortimer J.; Carr, Peter W.; Taft, R. W.; Abraham, Michael H.; Journal of the American Chemical Society; vol. 103; nb. 20; (1981); p. 6062 - 6066, View in Reaxys

By formation of salt/complex with THF. Additional data: free energie

Kamlet, Mortimer J.; Carr, Peter W.; Taft, R. W.; Abraham, Michael H.; Journal of the American Chemical Society; vol. 103; nb. 20; (1981); p. 6062 - 6066, View in Reaxys

By formation of salt/complex with 2-butanone. Additional data: free energie

Kamlet, Mortimer J.; Carr, Peter W.; Taft, R. W.; Abraham, Michael H.; Journal of the American Chemical Society; vol. 103; nb. 20; (1981); p. 6062 - 6066, View in Reaxys

By formation of salt/complex with acetone. Additional data: free energie

Kamlet, Mortimer J.; Carr, Peter W.; Taft, R. W.; Abraham, Michael H.; Journal of the American Chemical Society; vol. 103; nb. 20; (1981); p. 6062 - 6066, View in Reaxys

By formation of salt/complex with DMF. Additional data: free energie

Kamlet, Mortimer J.; Carr, Peter W.; Taft, R. W.; Abraham, Michael H.; Journal of the American Chemical Society; vol. 103; nb. 20; (1981); p. 6062 - 6066, View in Reaxys

By formation of salt/complex with DMSO. Additional data: free energie

Kamlet, Mortimer J.; Carr, Peter W.; Taft, R. W.; Abraham, Michael H.; Journal of the American Chemical Society; vol. 103; nb. 20; (1981); p. 6062 - 6066, View in Reaxys

By formation of salt/complex with cyclohexanone. Additional data: free energie

Kamlet, Mortimer J.; Carr, Peter W.; Taft, R. W.; Abraham, Michael H.; Journal of the American Chemical Society; vol. 103; nb. 20; (1981); p. 6062 - 6066, View in Reaxys

Komplex 1:1 mit Propylamin (Hgebunden) in Aceton: K(1), K(2), 38grad; Geschw.-Konst. (> k1, k3, <- k2, k4), (aus 1HNMR)

Ryzhova et al.; Russian Journal of Physical Chemistry; vol. 53; (1979); p. 261; ; p. 478, View in Reaxys

Komplex 1:2 mit Propylamin (Hgebunden) in Aceton: K(1), K(2), 38grad;

Ryzhova et al.; Russian Journal of Physical Chemistry; vol. 53; (1979); p. 261; ; p. 478, View in Reaxys

16/412

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Geschw.-Konst. (> k1, k3, <- k2, k4), (aus 1HNMR) CH3NO2*DNO3: IR, Raman (Fig. 2,2bis,3,4, Tab.I)

Diop et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 73; (1976); p. 207,208-211, View in Reaxys

Komplexe m. Donoren: o-, m- Toluidin: K in Aceton, CCl4, Cyclohexan (aus 1H-NMR)

Kobets et al.; Russian Journal of Physical Chemistry; vol. 50; (1976); p. 1295; ; p. 2152, View in Reaxys

CH3NO2*HNO3: F=-58.5+-0.2grad (Zustandsdiagramm Fig.1); IR, Raman (Fig. 2,2bis,3,4,5, Tab.I); Komplexbildungskonstanten (Tab.II); ΔH, ΔS Komplexbildung (Fig.6)

Diop et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 73; (1976); p. 207,208-211, View in Reaxys

Komplex mit Acn.: ΔH

Pang; Ng; Spectroscopy Letters; vol. 7; (1974); p. 511,515, View in Reaxys

Komplexbldg. m. 1,4,7,10,13,16Hexaoxa-cyclooctadecan (Raman), S.2156, 2157

McLachlan; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 30; (1974); p. 2153, View in Reaxys

Na-Salz: 1H-NMR (S.169)

Lorberth; Lange; Journal of Organometallic Chemistry; vol. 54; (1973); p. 165,167, 170, View in Reaxys

Einlagerungsverb. mit Mg-Uvanit

Hilke et al.; Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie; vol. 28; (1973); p. 239,244, View in Reaxys

1:1-Komplex mit HClO4: K, ΔH, ΔS

Belin; Potier; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 70; (1973); p. 490,493-495, View in Reaxys

Komplex mit SbCl5: 121SbMoessbauer-Parameter

Friedt et al.; Journal of Chemical Physics; vol. 59; (1973); p. 4468,4470, View in Reaxys

1:1-Komplex mit DClO4 (IR, Raman-Sp.)

Belin; Potier; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 69; (1972); p. 1222,1223,1224,1226,1227, View in Reaxys

1:1-Komplex mit HClO4 (IR, Raman-Sp.)

Belin; Potier; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 69; (1972); p. 1222,1223,1224,1226,1227, View in Reaxys

DCl-Addukt: Temperaturabhaengigkeit d. NMR (Fig. 3)

Tegenfeldt; Acta Chemica Scandinavica (1947-1973); vol. 26; (1972); p. 3524, View in Reaxys

Akzeptor-Komplex mit HF: HFFrequenz bei 20grad; Komplexbldg. Enthalpie

Touhara et al.; Journal of Physical Chemistry; vol. 75; (1971); p. 2222, View in Reaxys

Komplex mit HF: IR

Huong; Couzi; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 67; (1970); p. 1994,1996, 1997, View in Reaxys

<CH2NO2>-Na+: NMR

Witanowski; Shevelev; Journal of Molecular Spectroscopy; vol. 33; (1970); p. 19,20, View in Reaxys

17/412

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Komplex /BRN= 944519/ mit SO3. Gleichgew'konst. K= 12.5 l/mol. NMR (Fig.1)

1-ethyl-4-methoxy-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid 4-sulfamoylphenethylamide

Cerfontain; Koeberg-Telder; Recueil des Travaux Chimiques des Pays-Bas; vol. 89; (1970); p. 569,570, View in Reaxys

H-Komplex mit Phenol

Rassadin; Iogansen; Journal of Applied Spectroscopy; vol. 10; (1969); p. 203; ; p. 290, View in Reaxys

Na-Salz: IR- und Raman-Sp.

Brookes; Jonathan; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 25; (1969); p. 187,188, View in Reaxys

Assoz. m. CHCl3 und CDCl3

Devaure et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 65; (1968); p. 1064, View in Reaxys

Na-Salz: IR,Raman, Grundschw.

Brookes; Jonathan; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1968); p. 1529, View in Reaxys

Clathrat: 2CH3NO2*Diamin (C18H20O2): Dielektrizitaetskonstante;Meakins zitiert bei

Davies; Williams; Transactions of the Faraday Society; vol. 64; (1968); p. 529,543, View in Reaxys

Clathrat: 2CH3NO2*Diamin (C18H20O2): Dielktrizitaetskonstante bei 20grad und den Frequenzen 160 kHz und 8.5 GHz; dielektrischer Verlust bei der Frequenz 8.5 GHz und 20grad

Davies; Williams; Transactions of the Faraday Society; vol. 64; (1968); p. 529,543, View in Reaxys

Assoz. m. CH3COOH

Haurie; Novak; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 64; (1967); p. 679, View in Reaxys

Assoziation mit JBr (2442)

Yagi et al.; Journal of Physical Chemistry; vol. 71; (1967); p. 2439, View in Reaxys

Komplex mit Iod: UV, Bildungskonstante

Pyle et al.; Journal of Organic Chemistry; vol. 32; (1967); p. 3667, View in Reaxys

<ClO2(ClO4)2(C H3NO2)2>: Cl-OBindungsenergie

Vdovenko et al.; Doklady Chemistry; vol. 172-177; (1967); p. 340; Doklady Akademii Nauk SSSR; vol. 174; (1967); p. 382, View in Reaxys

SbCl5*CH3NO2: F:84-85grad; gelb; IR; RamanSp.; Debyeogramm

Riesel; Lehmann; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 7; (1967); p. 316, View in Reaxys

SbCl5*CH3NO2: F:84-85grad (s.dagegen: Paul et al., J.Indian Chem.Soc. 42(7)<1965>483: F:55grad); gelb

Riesel; Lehmann; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 7; (1967); p. 316, View in Reaxys

Kompl. mit Bzl.:Spektroskop. ermittelte Gleichgewichtskonst. in Hexan bei 25grad

Weimer; Prausnitz; Spectrochimica Acta; vol. 22; (1966); p. 77,79, View in Reaxys

Komplex mit pXylol: spektros-

Weimer; Prausnitz; Spectrochimica Acta; vol. 22; (1966); p. 77,79, View in Reaxys

18/412

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kop. ermittelte Gleichgewichtskonst. in Hexan bei 25grad Komplex mit Mesitylen: spektroskop. ermittelte Gleichgewichtskonstante in Hexan bei 25grad

Weimer; Prausnitz; Spectrochimica Acta; vol. 22; (1966); p. 77,79, View in Reaxys

TiF4*CH3NO2

Paul et al.; Journal of the Indian Chemical Society; vol. 42; (1965); p. 483,492, View in Reaxys

AsCl3*CH3NO2

Paul et al.; Journal of the Indian Chemical Society; vol. 42; (1965); p. 483,492, View in Reaxys

MnCl2*CH3NO2

Paul et al.; Journal of the Indian Chemical Society; vol. 42; (1965); p. 483,492, View in Reaxys

SnCl4*CH3NO2

Paul et al.; Journal of the Indian Chemical Society; vol. 42; (1965); p. 483,492, View in Reaxys

TiCl4*CH3NO2

Paul et al.; Journal of the Indian Chemical Society; vol. 42; (1965); p. 483,492, View in Reaxys

SbCl3*2CH3NO2

Paul et al.; Journal of the Indian Chemical Society; vol. 42; (1965); p. 483,492, View in Reaxys

SnCl4*2CH3NO2

Paul et al.; Journal of the Indian Chemical Society; vol. 42; (1965); p. 483,492, View in Reaxys

2CdCl2*CH3NO2

Paul et al.; Journal of the Indian Chemical Society; vol. 42; (1965); p. 483,492, View in Reaxys

2CuCl2*CH3NO2

Paul et al.; Journal of the Indian Chemical Society; vol. 42; (1965); p. 483,492, View in Reaxys

2HgCl2*CH3NO2

Paul et al.; Journal of the Indian Chemical Society; vol. 42; (1965); p. 483,492, View in Reaxys

2NiCl2*CH3NO2

Paul et al.; Journal of the Indian Chemical Society; vol. 42; (1965); p. 483,492, View in Reaxys

2ZnCl2*CH3NO2

Paul et al.; Journal of the Indian Chemical Society; vol. 42; (1965); p. 483,492, View in Reaxys

SbCl3*CH3NO2: F: 63grad

Paul et al.; Journal of the Indian Chemical Society; vol. 42; (1965); p. 483,492, View in Reaxys

CaCl2*CH3NO2: F: >250grad

Paul et al.; Journal of the Indian Chemical Society; vol. 42; (1965); p. 483,492, View in Reaxys

Komplexbildung mit Ammoniak

Datta; Barrow; Journal of the American Chemical Society; vol. 87; (1965); p. 3053,3054, View in Reaxys

Na-Salz: IR-Sp. (KBr); NMR-Sp.

Griswold,A.A.; Starcher,P.S.; Journal of Organic Chemistry; vol. 30; (1965); p. 1687 1690, View in Reaxys

H2SO4*CH3NO2: spez. Leitfaehigk. bei 30grad

Paul et al.; Journal of the Indian Chemical Society; vol. 42; (1965); p. 483,492, View in Reaxys

HSO3F*CH3NO2: spez. Leitfaehigkeit b. 30grad

Paul et al.; Journal of the Indian Chemical Society; vol. 42; (1965); p. 483,492, View in Reaxys

H2SO4*2CH3NO 2: spez. Leitfaehigkeit b. 30grad

Paul et al.; Journal of the Indian Chemical Society; vol. 42; (1965); p. 483,492, View in Reaxys

SbCl5*CH3NO2: F: 55grad; gelb; spez. Leitfaehigkeit bei 55grad

Paul et al.; Journal of the Indian Chemical Society; vol. 42; (1965); p. 483,492, View in Reaxys

19/412

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Na-Salz: 14NNMR

Herbison-Evans; Richards; Molecular Physics; vol. 8; (1964); p. 19,26, View in Reaxys

NaSalz:CH2NNaO2: IR-Sp. (2-40μ); Struktur

Yarwood; Orville-Thomas; Journal of the Chemical Society; (1963); p. 5991, View in Reaxys

Natriumsalz: Charakteristische IR-Banden

Feuer,H. et al.; Spectrochimica Acta; vol. 19; (1963); p. 431 - 434, View in Reaxys

Natrium-Salz: IRSpektrum:

Jonathan; Journal of Molecular Spectroscopy; vol. 7; (1961); p. 105,108, View in Reaxys

Verb. mit 1Mol Aminoessigsaeure u. 1 Mol SnCl4: aus 1Mol Aminoessigsaeure in Nitromethan , 1Mol SnCl4

Sumarokowa; Litwiak; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 352,316; Chem.Abstr.; nb. 24365; (1961), View in Reaxys

as nitroformaldehyde phenylhydrazone (mp: 92 degree ), as C-nitro-N,N'-diphenylformazan (mp: 153 degree ) and as nitroformaldehyde-<4-nitrophenylhydrazone> (mp: 159 degree )

Slebodzinski; Makaruk; Bulletin de l'Academie Polonaise des Sciences, Classe 3: Mathematique, Astronomie, Physique, Chimie, Geologie et Geographie; vol. 3; (1955); p. 377,378, View in Reaxys

strychnine salt; Further Data see Handbook (IR Spectrum)

Chatten et al.; Journal of the American Pharmaceutical Association (1912-1977); vol. 44; (1955); p. 332,335, View in Reaxys

Purification (1) References Kemula; Brzozowski; Roczniki Chemii; vol. 35; (1961); p. 711,715, View in Reaxys Melting Point (12) 1 of 12

Melting Point [°C]

-28

Bagryanskaya, Yu. i.; Gatilov, Yu. V.; Journal of Structural Chemistry; vol. 24; nb. 1; (1983); p. 150 - 151; Zhurnal Strukturnoi Khimii; vol. 24; nb. 1; (1983); p. 158 - 160, View in Reaxys 2 of 12

Melting Point [°C]

-28.55

Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys 3 of 12

Melting Point [°C]

-30.04

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys 4 of 12

Melting Point [°C]

-28.37

Comment (Melting Point)

F=-28.37+-0.05grad (mit CaSO4 getrocknetes Praeparat).

Jones; Giauque; Journal of the American Chemical Society; vol. 69; (1947); p. 984, View in Reaxys 5 of 12

Melting Point [°C]

-28.6

Smyth; Walls; J.chim.Physics; vol. 3; (1935); p. 557, View in Reaxys; Timmermans; Hennaut-Roland; Journal of Chemical Physics; vol. 29; (1932); p. 562, View in Reaxys 6 of 12

Melting Point [°C]

-28.6 - -15

Deffet; Bulletin des Societes Chimiques Belges; vol. 44; (1935); p. 69, View in Reaxys

20/412

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7 of 12

Comment (Melting Point)

Melting point:Erstarrungstemperaturen zwischen 1 atm und 990 atm.

Deffet; Bulletin des Societes Chimiques Belges; vol. 44; (1935); p. 69, View in Reaxys 8 of 12

Melting Point [°C]

-29.2

Timmermans; Bulletin des Societes Chimiques Belges; vol. 30; (1921); p. 70; Chem. Zentralbl.; vol. 92; nb. III; (1921); p. 289, View in Reaxys 9 of 12

Melting Point [°C]

-17

Jaeger; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 101; (1917); p. 66, View in Reaxys 10 of 12

Melting Point [°C]

-26.5

Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 73; (1910); p. 261, View in Reaxys 11 of 12

Melting Point [°C]

-28.5

Henry; Chem. Zentralbl.; vol. 78; nb. I; (1907); p. 1312, View in Reaxys 12 of 12

Melting Point [°C]

-25.5

Holleman,M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 23; (1904); p. 299, View in Reaxys Boiling Point (43) Boiling Point [°C] Pressure (Boiling Point) [Torr] 30

0.90009

Location

Comment (Boiling References Point)

supporting information

Quinet, Coralie; Sampoux, Laetitia; Marko, Istvan E.; European Journal of Organic Chemistry; nb. 11; (2009); p. 1806 - 1811, View in Reaxys

95 - 100

Saifullina; Grebenyuk; Stempnevskaya; Valikhanov; Vinogradova; Levkovich; Tashmukhamedova; Chemistry of Natural Compounds; vol. 34; nb. 6; (1998); p. 711 - 714, View in Reaxys

100.2

Aminabhavi, T. M.; Manjeshwar, L. S.; Balundgi, R. H.; Journal of Chemical & Engineering Data; vol. 32; nb. 1; (1987); p. 50 - 52, View in Reaxys

98 - 100

Ibragimov, A. A.; Yunusov, S. Yu.; Chemistry of Natural Compounds; vol. 21; nb. 4; (1985); p. 502 - 509; Khimiya Prirodnykh Soedinenii; vol. 21; nb. 4; (1985); p. 536 - 544, View in Reaxys

101

Cadogan,J.I.G.; Inward,P.W.; Journal of the Chemical Society; (1962); p. 4170 - 4178, View in Reaxys; Bowers et al.; Journal of Inorganic and Nuclear Chemistry; vol. 33; (1971); p. 81,83, 85, View in Reaxys; Ishida et al.; Bulletin of the Chemical Society of Japan; vol. 43; (1970); p. 285, View in Reaxys; Geiseler et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 1007,1008, View in Reaxys; Sakodynsky et al.; Analytical Chemistry; vol. 45; (1973); p. 1369,1372, View in Reaxys; Yoshida; Takabayashi; Nippon Kagaku Zasshi; vol. 87; (1966); p. 452,453,454, View in Reaxys; Regis; Corset; Canadian Journal of Chemistry; vol. 51; (1973); p. 3577,3582, 3584, 3585, View in Reaxys; Zhuravleva et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 46; (1976); p. 1210,1194,1195,1196,1197, View in Reaxys; Novikov, V. F.; Nurtdinov, S. Kh.; Vigdergauz, M. S.; J. Gen. Chem. USSR (Engl. Transl.); vol. 51; nb. 3; (1981); p. 579 - 584,456 - 460, View in Reaxys

21/412

2016-04-19 03:35:30

101.3

Badoni; Bhagat; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 14; (1976); p. 905, View in Reaxys; Zhuravleva; Zhukova; J. Gen. Chem. USSR (Engl. Transl.); vol. 47; (1977); p. 1942,1777, View in Reaxys; Zhuravleva et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 47; (1977); p. 1686,1545, View in Reaxys; Zhuravleva; Mukhametshin; J. Gen. Chem. USSR (Engl. Transl.); vol. 49; (1979); p. 1217,1067, View in Reaxys; Kudryavtseva; Eizen; J. Appl. Chem. USSR (Engl. Transl.); vol. 43; (1970); p. 708,716, View in Reaxys

99 - 101

Urisbaev et al.; J. Anal. Chem. USSR (Engl. Transl.); vol. 33; (1978); p. 1714,1716, View in Reaxys

100

Sutyagina et al.; Russian Journal of Physical Chemistry; vol. 51; (1977); p. 1820; ; p. 3117, View in Reaxys

100 - 101

Meek; Ehrhardt; Inorganic Chemistry; vol. 4; (1965); p. 584, View in Reaxys; Meek; Inorganic Chemistry; vol. 4; (1965); p. 250, View in Reaxys; Matrosov et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 25; (1976); p. 295,298; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 25; (1976); p. 313, View in Reaxys

Mauret et al.; Bulletin de la Societe Chimique de France; (1974); p. 379, View in Reaxys

715

Owensby et al.; Journal of the American Chemical Society; vol. 96; (1974); p. 2682,2684,2685,2686, View in Reaxys

100.5 - 101

Beames; Mander; Australian Journal of Chemistry; vol. 27; (1974); p. 1257,1263, View in Reaxys

101 - 102

Korb; Fernandez; Journal of Chemical and Engineering Data; vol. 16; (1971); p. 108, View in Reaxys; Ellert et al.; Acta Poloniae Pharmaceutica; vol. 17; (1960); p. 29,31; Chem.Abstr.; vol. 54; nb. 11806; (1960), View in Reaxys

101 - 102

760

Matasa; Hass; Canadian Journal of Chemistry; vol. 49; (1971); p. 1284,1287, View in Reaxys

100.5

760

Obolenzew et al.; Neftekhimiya; vol. 11; (1971); p. 893,256; Chem.Abstr.; nb. 46754; (1969), View in Reaxys

100.5 - 101.5 33 - 33.5

Dutta et al.; Inorganic Chemistry; vol. 9; (1970); p. 1215,1216, View in Reaxys 94 - 95

Tenno; Talvik; Organic Reactivity (New York, English Translation); vol. 6; (1969); p. 383, View in Reaxys

100.7

Borowitz; Parnes; Journal of Organic Chemistry; vol. 32; (1967); p. 3560, View in Reaxys

Fischer et al.; Pharmazeutische Zentralhalle; vol. 105; (1966); p. 73,74, View in Reaxys

27.2 - 27.4

Sargla et al.; Organic Reactivity (New York, English Translation); vol. 3; (1966); p. 180, View in Reaxys

22/412

2016-04-19 03:35:30

101.2

Tolstova et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 38; (1965); p. 2617,2558, View in Reaxys

101

761

Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys

Riley; Rothstein; Journal of the Chemical Society; (1964); p. 3860,3862, View in Reaxys

101.2

760

Schuberth; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 225; (1964); p. 305,307, View in Reaxys

101

760

Overberger; Kamath; Journal of the American Chemical Society; vol. 85; (1963); p. 446, View in Reaxys

101 - 101.5

Sutton; Australian Journal of Chemistry; vol. 16; (1963); p. 278,279, View in Reaxys; Sutton; Australian Journal of Chemistry; vol. 16; (1963); p. 1134, View in Reaxys; Sutton; Australian Journal of Chemistry; vol. 14; (1961); p. 37,39, View in Reaxys; Sutton; Australian Journal of Chemistry; vol. 15; (1962); p. 563,565, View in Reaxys

100.2 - 100.4

Tarnawski; Monatshefte fuer Chemie; vol. 93; (1962); p. 884,887, View in Reaxys

Kartnig; Scientia Pharmaceutica; vol. 29; (1961); p. 187,188, View in Reaxys

97.5

697.3

Sumarokowa; Litwiak; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 352,316; Chem.Abstr.; nb. 24365; (1961), View in Reaxys

101.02

760

Brown; Smith; Australian Journal of Chemistry; vol. 13; (1960); p. 30, View in Reaxys

101.6 - 102

765.5

Clarke; Rothwell; Journal of the Chemical Society; (1960); p. 1885,1887, View in Reaxys

98 - 101

Fischer et al.; Pharmazeutische Zentralhalle; vol. 99; (1960); p. 299,310, View in Reaxys

101.2

760

99.98

760

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys

101

762

Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys

101.5

762

Smyth; Walls; J.chim.Physics; vol. 3; (1935); p. 557, View in Reaxys

101.25

760

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 558, View in Reaxys

101.15

760

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 20, View in Reaxys; Lattey; Gatty; Phil.Mag.; vol. <7>7; p. 1000, View in Reaxys

100.76 - 100.86

760

Ueber Phosphor- Williams; Journal of the American Chemical Sopentoxyd getrock- ciety; vol. 47; (1925); p. 2646, View in Reaxys net.

101 - 101.5

764.7

Schiff,R.; Chemische Berichte; vol. 19; (1886); p. 567, View in Reaxys

88.23

507.5

Dreisbach; Shrader; Industrial and Engineering Chemistry; vol. 41; p. 2879, View in Reaxys

extrapoliert.

23/412

Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys

2016-04-19 03:35:30

74.25

315.5

Dreisbach; Shrader; Industrial and Engineering Chemistry; vol. 41; p. 2879, View in Reaxys

50.85

123.8

Dreisbach; Shrader; Industrial and Engineering Chemistry; vol. 41; p. 2879, View in Reaxys

Refractive Index (67) Refractive Index Wavelength (Refractive Index) [nm]

Temperature (Refractive Index) [°C]

References

1.3786

632.8

24.163

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys

1.379

632.8

23.269

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys

1.3795

632.8

22.216

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys

1.3799

632.8

21.384

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys

1.3804

632.8

20.372

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys

1.3808

632.8

19.423

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys

1.3808

632.8

19.446

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys

1.3812

632.8

18.545

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys

1.3817

632.8

17.598

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys

1.3795

589

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys; Ponomarenko, S. M.; Mushtakova, S. P.; Demakhin, A. G.; Faifel', B. L.; Kal'manovich, D. G.; Russian Journal of General Chemistry; vol. 65; nb. 2.1; (1995); p. 160 - 167; Zhurnal Obshchei Khimii; vol. 65; nb. 2; (1995); p. 190 198, View in Reaxys

1.38165

589

Feng, Hui; Wang, Yanru; Shi, Jun; Benson, George C.; Lu, Benjamin C.-Y.; Journal of Chemical Thermodynamics; vol. 23; nb. 2; (1991); p. 169 - 174, View in Reaxys

1.3817

589

Moll; Koll.Beih.; vol. 49; (1939); p. 7, View in Reaxys; Gabriel; Industrial and Engineering Chemistry; vol. 32; (1940); p. 891, View in Reaxys; Graja; Roczniki Chemii; vol. 47; (1973); p. 1683,1684, View in Reaxys; Korosi; Kovats; Journal of Chemical and Engineering Data; vol. 26; nb. 3; (1981); p. 323 - 332, View in Reaxys

1.382

589

Markusin; Nikanorowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 32; (1962); p. 3469,3407, View in Reaxys; Zhuravleva; Zhuravlev; J. Gen. Chem. USSR (Engl. Transl.); vol. 47; (1977); p. 1939,1774, View in Reaxys; Zhuravleva; Zhukova; J. Gen. Chem. USSR (Engl. Transl.); vol. 47; (1977); p. 1942,1777, View in Reaxys; Zhuravleva et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 46; (1976); p. 1210,1194,1195,1196,1197, View in Reaxys; Sazonov et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 48; (1975); p. 1953,2025, View in Reaxys; Zhuravleva et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 47; (1977); p. 1686,1545, View in Reaxys; Zhuravleva; Mukhametshin; J. Gen. Chem. USSR (Engl. Transl.); vol. 49;

24/412

2016-04-19 03:35:30

(1979); p. 1217,1067, View in Reaxys; Zhuravleva et al.; Russian Journal of Physical Chemistry; vol. 49; (1975); p. 1530; ; p. 2609, View in Reaxys; Kudryavtseva; Eizen; J. Appl. Chem. USSR (Engl. Transl.); vol. 43; (1970); p. 708,716, View in Reaxys 1.3797

589

Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 59; (1907); p. 394; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 65; (1909); p. 143, View in Reaxys; Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys; Clever; Hsu; Journal of Chemical Thermodynamics; vol. 10; (1978); p. 213,214, 216 - 218, View in Reaxys

1.3813

589

Sutyagina et al.; Russian Journal of Physical Chemistry; vol. 51; (1977); p. 1820; ; p. 3117, View in Reaxys

1.3768

589

Mauret et al.; Bulletin de la Societe Chimique de France; (1974); p. 379, View in Reaxys

1.3819

589

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys; Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys; Schuberth; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 225; (1964); p. 305,307, View in Reaxys; Boublikova; Collection of Czechoslovak Chemical Communications; vol. 38; (1973); p. 2033, View in Reaxys; Tarnawski; Monatshefte fuer Chemie; vol. 93; (1962); p. 884,887, View in Reaxys

1.4304

589

Boublikova; Collection of Czechoslovak Chemical Communications; vol. 38; (1973); p. 2033, View in Reaxys Lelikova et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 43; (1973); p. 1300,1291,1292, View in Reaxys; Derrick; Clever; Journal of Physical Chemistry; vol. 75; (1971); p. 3728, View in Reaxys

1.3818

589

Holcomb; Dorsey; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2788, View in Reaxys; Tolstova et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 38; (1965); p. 2617,2558, View in Reaxys; Matasa; Hass; Canadian Journal of Chemistry; vol. 49; (1971); p. 1284,1287, View in Reaxys; Tenno; Talvik; Organic Reactivity (New York, English Translation); vol. 6; (1969); p. 383, View in Reaxys; Sargla et al.; Organic Reactivity (New York, English Translation); vol. 3; (1966); p. 180, View in Reaxys

1.38

589

Gorodyskii; Bakhshiev; Theoretical and Experimental Chemistry; vol. 7; (1971); p. 513,515, View in Reaxys

1.3815

589

Obolenzew et al.; Neftekhimiya; vol. 11; (1971); p. 893,256; Chem.Abstr.; nb. 46754; (1969), View in Reaxys

1.394

Fowler et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1971); p. 460, View in Reaxys

1.3935

589

Geiseler et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 1007,1008, View in Reaxys

1.3812

589

Rodina; Khaldna; Organic Reactivity (New York, English Translation); vol. 4; (1967); p. 74, View in Reaxys

1.3883

589

Fischer et al.; Pharmazeutische Zentralhalle; vol. 105; (1966); p. 73,74, View in Reaxys; Fischer et al.; Pharmazeutische Zentralhalle; vol. 99; (1960); p. 299,310, View in Reaxys

1.3816

589

Williams et al.; Journal of Organic Chemistry; vol. 30; (1965); p. 2674,2675, View in Reaxys

1.368

589

Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys

1.3805

589

Overberger; Kamath; Journal of the American Chemical Society; vol. 85; (1963); p. 446, View in Reaxys

1.37954

589

Brown; Smith; Australian Journal of Chemistry; vol. 15; (1962); p. 1,3, View in Reaxys

25/412

2016-04-19 03:35:30

1.3831

589

Kartnig; Scientia Pharmaceutica; vol. 29; (1961); p. 187,188, View in Reaxys

1.37964

589

Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys; Brown; Smith; Australian Journal of Chemistry; vol. 13; (1960); p. 30, View in Reaxys

1.37738

589

Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys

1.38188

589

Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys

1.3773

589

Thompson et al.; Journal of the American Chemical Society; vol. 76; (1954); p. 3445, View in Reaxys

1.37963

589

Thompson et al.; Journal of the American Chemical Society; vol. 76; (1954); p. 3445, View in Reaxys

1.38197

589

Thompson et al.; Journal of the American Chemical Society; vol. 76; (1954); p. 3445, View in Reaxys

435.8 - 667.8

Thompson et al.; Journal of the American Chemical Society; vol. 76; (1954); p. 3445, View in Reaxys

435.8 - 667.8

Thompson et al.; Journal of the American Chemical Society; vol. 76; (1954); p. 3445, View in Reaxys

435.8 - 667.8

Thompson et al.; Journal of the American Chemical Society; vol. 76; (1954); p. 3445, View in Reaxys

1.37895

656.3

Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys

1.38152

589

Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys

1.38778

486.1

Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys

1.3927

434

Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys

1.3787

589

Boyd; Copeland; Journal of the American Chemical Society; vol. 64; (1942); p. 2542, View in Reaxys

1.3824

589

Wiswall; Smyth; Journal of Chemical Physics; vol. 9; (1941); p. 357, View in Reaxys

1.3797

589

Smyth; Walls; Journal of Chemical Physics; vol. 3; (1935); p. 557, View in Reaxys

1.3839

587.6

Joukovsky; Bulletin des Societes Chimiques Belges; vol. 43; (1934); p. 401, View in Reaxys

1.3809

667

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 558, View in Reaxys

1.38139

656

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 558, View in Reaxys

1.38411

587.6

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 558, View in Reaxys

1.38911

492

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 558, View in Reaxys

1.39058

486

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 558, View in Reaxys

1.39462

447

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 558, View in Reaxys

546

Eisele; Annalen der Physik (Weinheim, Germany); vol. <4> 76; (1925); p. 400, View in Reaxys

589

Eisele; Annalen der Physik (Weinheim, Germany); vol. <4> 76; (1925); p. 400, View in Reaxys

26/412

2016-04-19 03:35:30

656

Eisele; Annalen der Physik (Weinheim, Germany); vol. <4> 76; (1925); p. 400, View in Reaxys

1.38283

589

17.1

Eisele; Annalen der Physik (Weinheim, Germany); vol. <4> 76; (1925); p. 400, View in Reaxys

1.38056

589

Williams; Journal of the American Chemical Society; vol. 47; (1925); p. 2646, View in Reaxys

1.37997

656.3

18.8

Cotton; Mouton; Annales de Chimie (Cachan, France); vol. <8> 28; (1913); p. 215, View in Reaxys

1.38242

589

18.8

Cotton; Mouton; Annales de Chimie (Cachan, France); vol. <8> 28; (1913); p. 215, View in Reaxys

1.38889

486.1

18.8

Cotton; Mouton; Annales de Chimie (Cachan, France); vol. <8> 28; (1913); p. 215, View in Reaxys

1.39348 1.39358

589

Henry; Chem. Zentralbl.; vol. 78; nb. I; (1907); p. 1312, View in Reaxys

1.37884

656.3

21.6

Bruehl; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 16; (1895); p. 214; Chemische Berichte; vol. 26; (1893); p. 2515, View in Reaxys

1.38133

589

21.6

Bruehl; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 16; (1895); p. 214; Chemische Berichte; vol. 26; (1893); p. 2515, View in Reaxys

1.38771

486.1

21.6

Bruehl; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 16; (1895); p. 214; Chemische Berichte; vol. 26; (1893); p. 2515, View in Reaxys

1.39305

434

21.6

Bruehl; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 16; (1895); p. 214; Chemische Berichte; vol. 26; (1893); p. 2515, View in Reaxys

Density (98) 1 of 98

Density [g·cm-3]

1.13117

Measurement Temperature [°C]

24.991

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys 2 of 98

Density [g·cm-3]

1.13253

Measurement Temperature [°C]

23.991

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys 3 of 98

Density [g·cm-3]

1.13389

Measurement Temperature [°C]

22.991

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys 4 of 98

Density [g·cm-3]

1.13524

Measurement Temperature [°C]

21.991

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys 5 of 98

Density [g·cm-3]

1.1366

Measurement Temperature [°C]

20.991

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys 6 of 98

Density [g·cm-3]

1.13795

27/412

2016-04-19 03:35:30

Measurement Temperature [°C]

19.991

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys 7 of 98

Density [g·cm-3]

1.13931

Measurement Temperature [°C]

18.991

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys 8 of 98

Density [g·cm-3]

1.14066

Measurement Temperature [°C]

17.991

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys 9 of 98

Density [g·cm-3]

1.14201

Measurement Temperature [°C]

16.991

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys 10 of 98

Density [g·cm-3]

1.14337

Measurement Temperature [°C]

15.991

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys 11 of 98

Density [g·cm-3]

1.14472

Measurement Temperature [°C]

14.991

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys 12 of 98

Density [g·cm-3]

1.14607

Measurement Temperature [°C]

13.991

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys 13 of 98

Density [g·cm-3]

1.14742

Measurement Temperature [°C]

12.991

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys 14 of 98

Density [g·cm-3]

1.14877

Measurement Temperature [°C]

11.991

Shi, Shaoxiong; Xu, Chen; Yin, Tianxiang; Chen, Zhiyun; Shen, Weiguo; Journal of Molecular Liquids; vol. 207; (2015); p. 152 - 158, View in Reaxys 15 of 98

Density [g·cm-3]

1.13059

Measurement Temperature [°C]

24.99

Comment (Density)

Liquid

Kiselev, Vladimir D.; Kashaeva, Helena A.; Shakirova, Ilzida I.; Potapova, Lubov N.; Konovalov, Alexander I.; Journal of Solution Chemistry; vol. 41; nb. 8; (2012); p. 1375 - 1387,13, View in Reaxys

28/412

2016-04-19 03:35:30

16 of 98

Density [g·cm-3]

1.13792

Measurement Temperature [°C]

19.99

Comment (Density)

1.13792 - 1.13798 g/cm3

Iglesias-Otero, Manuel A.; Troncoso, Jacobo; Carballo, Enrique; Romani, Luis; Journal of Chemical and Engineering Data; vol. 53; nb. 6; (2008); p. 1298 - 1301, View in Reaxys 17 of 98

Density [g·cm-3]

1.12432

Measurement Temperature [°C]

29.99

Comment (Density)

1.12432 - 1.12439 g/cm3

Iglesias-Otero, Manuel A.; Troncoso, Jacobo; Carballo, Enrique; Romani, Luis; Journal of Chemical and Engineering Data; vol. 53; nb. 6; (2008); p. 1298 - 1301, View in Reaxys 18 of 98

Density [g·cm-3]

1.11062

Measurement Temperature [°C]

39.99

Comment (Density)

1.11062 - 1.11068 g/cm3

Iglesias-Otero, Manuel A.; Troncoso, Jacobo; Carballo, Enrique; Romani, Luis; Journal of Chemical and Engineering Data; vol. 53; nb. 6; (2008); p. 1298 - 1301, View in Reaxys 19 of 98

Density [g·cm-3]

1.09682

Measurement Temperature [°C]

49.99

Comment (Density)

1.09682 - 1.09688 g/cm3

Iglesias-Otero, Manuel A.; Troncoso, Jacobo; Carballo, Enrique; Romani, Luis; Journal of Chemical and Engineering Data; vol. 53; nb. 6; (2008); p. 1298 - 1301, View in Reaxys 20 of 98

Density [g·cm-3]

1.11654 - 1.13721

Measurement Temperature [°C]

20 - 35

Makowska, Anna; Szydlowski, Jerzy; Journal of Chemical and Engineering Data; vol. 50; nb. 4; (2005); p. 1365 1369, View in Reaxys 21 of 98

Density [g·cm-3]

1.1317

Measurement Temperature [°C]

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 22 of 98

Density [g·cm-3]

1.11614 - 1.14328

Measurement Temperature [°C]

15 - 35

Romani; Troncoso; Tovar; Cerdeirina; Carballo; Journal of Chemical and Engineering Data; vol. 46; nb. 2; (2001); p. 312 - 316, View in Reaxys 23 of 98

Density [g·cm-3]

1.13011

Measurement Temperature [°C]

Lorenzi, Lorenzo De; Fermeglia, Maurizio; Torriano, Giovanni; Journal of Chemical & Engineering Data; vol. 40; nb. 6; (1995); p. 1172 - 1177, View in Reaxys 24 of 98

Density [g·cm-3]

1.1311

Measurement Temperature [°C]

Ponomarenko, S. M.; Mushtakova, S. P.; Demakhin, A. G.; Faifel', B. L.; Kal'manovich, D. G.; Russian Journal of General Chemistry; vol. 65; nb. 2.1; (1995); p. 160 - 167; Zhurnal Obshchei Khimii; vol. 65; nb. 2; (1995); p. 190 198, View in Reaxys

29/412

2016-04-19 03:35:30

25 of 98

Density [g·cm-3]

1.13755

Measurement Temperature [°C]

Feng, Hui; Wang, Yanru; Shi, Jun; Benson, George C.; Lu, Benjamin C.-Y.; Journal of Chemical Thermodynamics; vol. 23; nb. 2; (1991); p. 169 - 174, View in Reaxys 26 of 98

Density [g·cm-3]

1.1225

Measurement Temperature [°C]

Dewan, R.K.; Sharma, A.K.; Mehta, S.K.; Journal of Solution Chemistry; vol. 17; nb. 5; (1988); p. 459 - 466, View in Reaxys 27 of 98

Density [g·cm-3]

1.10562

Measurement Temperature [°C]

Manjeshwar, Lata S.; Aminabhavi, Tejraj M.; Journal of Chemical & Engineering Data; vol. 32; nb. 4; (1987); p. 409 - 412, View in Reaxys 28 of 98

Density [g·cm-3]

1.1255

Measurement Temperature [°C]

Manjeshwar, Lata S.; Aminabhavi, Tejraj M.; Journal of Chemical & Engineering Data; vol. 32; nb. 4; (1987); p. 409 - 412, View in Reaxys 29 of 98

Density [g·cm-3]

1.08985 - 1.11078

Measurement Temperature [°C]

10 - 25

Davydova, O. I.; Afanas'ev, V. N.; Zhukov, B. A.; Krestov, G. A.; Russian Journal of Physical Chemistry; vol. 60; nb. 4; (1986); p. 583 - 585; Zhurnal Fizicheskoi Khimii; vol. 60; (1986); p. 982 - 984, View in Reaxys 30 of 98

Density [g·cm-3]

1.41

Type (Density)

crystallographic

Bagryanskaya, Yu. i.; Gatilov, Yu. V.; Journal of Structural Chemistry; vol. 24; nb. 1; (1983); p. 150 - 151; Zhurnal Strukturnoi Khimii; vol. 24; nb. 1; (1983); p. 158 - 160, View in Reaxys 31 of 98

Density [g·cm-3]

1.0594 - 1.1381

Measurement Temperature [°C]

20 - 80

Korosi; Kovats; Journal of Chemical and Engineering Data; vol. 26; nb. 3; (1981); p. 323 - 332, View in Reaxys 32 of 98

Density [g·cm-3]

1.401

Type (Density)

crystallographic

Trevino, S. F.; Prince, E.; Hubbard, C. R.; Journal of Chemical Physics; vol. 73; nb. 6; (1980); p. 2996 - 3000, View in Reaxys 33 of 98

Density [g·cm-3]

1.1369 - 1.1928

Measurement Temperature [°C]

-25.7 - 16.9

Vitali, Giovanni; Berchiesi, Gianfrancesco; Berchiesi, Maria A.; Gioia Lobbia, Giancarlo; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 77; nb. 9; (1980); p. 865 - 868, View in Reaxys 34 of 98

Density [g·cm-3]

1.132

Reference Temperature [°C]

Measurement Temperature [°C]

Zhuravleva; Zhuravlev; J. Gen. Chem. USSR (Engl. Transl.); vol. 47; (1977); p. 1939,1774, View in Reaxys; Zhuravleva; Zhukova; J. Gen. Chem. USSR (Engl. Transl.); vol. 47; (1977); p. 1942,1777, View in Reaxys; Zhuravleva et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 46; (1976); p. 1210,1194,1195,1196,1197, View in Reaxys; Zhuravleva et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 47; (1977); p. 1686,1545, View in Reaxys; Zhuravleva; Mu-

30/412

2016-04-19 03:35:30

khametshin; J. Gen. Chem. USSR (Engl. Transl.); vol. 49; (1979); p. 1217,1067, View in Reaxys; Zhuravleva et al.; Russian Journal of Physical Chemistry; vol. 49; (1975); p. 1530; ; p. 2609, View in Reaxys 35 of 98

Density [g·cm-3]

1.1198

Measurement Temperature [°C]

Clever; Hsu; Journal of Chemical Thermodynamics; vol. 10; (1978); p. 213,214, 216 - 218, View in Reaxys 36 of 98

Luzkii; Obuchowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 2692,2512; Chem.Abstr.; vol. 57; nb. 64; (1962), View in Reaxys; Berman; West; Journal of Chemical and Engineering Data; vol. 12; (1967); p. 197, View in Reaxys; Reese et al.; Journal of Chemical and Engineering Data; vol. 15; (1970); p. 140,141, View in Reaxys; Schroeder; Kintner; AIChE Journal; vol. 11; (1975); p. 5, View in Reaxys; Timofeeva et al.; Russian Journal of Physical Chemistry; vol. 52; (1978); p. 284; ; p. 496, View in Reaxys

37 of 98

Density [g·cm-3]

1.131

Reference Temperature [°C]

Measurement Temperature [°C]

Heubel,J. et al.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 15A; (1977); p. 687 - 690, View in Reaxys 38 of 98

Density [g·cm-3]

1.1309

Matrosov et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 25; (1976); p. 295,298; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 25; (1976); p. 313, View in Reaxys 39 of 98

Density [g·cm-3]

1.1381

Reference Temperature [°C]

Measurement Temperature [°C]

Sazonov et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 48; (1975); p. 1953,2025, View in Reaxys 40 of 98

Density [g·cm-3]

1.13825

Reference Temperature [°C]

Measurement Temperature [°C]

Khimenko et al.; Russian Journal of Physical Chemistry; vol. 49; (1975); p. 1407; ; p. 2400, View in Reaxys 41 of 98

Density [g·cm-3]

1.1388

Reference Temperature [°C]

Measurement Temperature [°C]

Tenno; Talvik; Organic Reactivity (New York, English Translation); vol. 6; (1969); p. 383, View in Reaxys 42 of 98

Density [g·cm-3]

1.1379

Reference Temperature [°C]

Measurement Temperature [°C]

Markusin; Nikanorowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 32; (1962); p. 3469,3407, View in Reaxys; Sargla et al.; Organic Reactivity (New York, English Translation); vol. 3; (1966); p. 180, View in Reaxys 43 of 98

Density [g·cm-3]

1.138

Reference Temperature [°C]

31/412

2016-04-19 03:35:30

Measurement Temperature [°C]

Tolstova et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 38; (1965); p. 2617,2558, View in Reaxys 44 of 98

Density [g·cm-3]

1.096

Reference Temperature [°C]

Measurement Temperature [°C]

Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys 45 of 98

Density [g·cm-3]

1.1306

Reference Temperature [°C]

Measurement Temperature [°C]

Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys 46 of 98

Density [g·cm-3]

1.1375

Reference Temperature [°C]

Measurement Temperature [°C]

Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys 47 of 98

Density [g·cm-3]

1.139

Measurement Temperature [°C]

Schuberth; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 225; (1964); p. 305,307, View in Reaxys 48 of 98

Density [g·cm-3]

1.1033

Reference Temperature [°C]

Measurement Temperature [°C]

Brown; Smith; Australian Journal of Chemistry; vol. 15; (1962); p. 1,3, View in Reaxys 49 of 98

Density [g·cm-3]

1.117

Reference Temperature [°C]

Measurement Temperature [°C]

Brown; Smith; Australian Journal of Chemistry; vol. 15; (1962); p. 1,3, View in Reaxys 50 of 98

Density [g·cm-3]

1.13063

Reference Temperature [°C]

Measurement Temperature [°C]

Brown; Smith; Australian Journal of Chemistry; vol. 15; (1962); p. 1,3, View in Reaxys 51 of 98

Density [g·cm-3]

1.308

Reference Temperature [°C]

Measurement Temperature [°C]

Brown; Smith; Australian Journal of Chemistry; vol. 13; (1960); p. 30, View in Reaxys

32/412

2016-04-19 03:35:30

52 of 98

Density [g·cm-3]

1.0551

Measurement Temperature [°C]

Rabinowitsch; Zhurnal Fizicheskoi Khimii; vol. 34; (1960); p. 423,424,425; engl.Ausg.; p. 198, View in Reaxys 53 of 98

Density [g·cm-3]

1.0694

Measurement Temperature [°C]

Rabinowitsch; Zhurnal Fizicheskoi Khimii; vol. 34; (1960); p. 423,424,425; engl.Ausg.; p. 198, View in Reaxys 54 of 98

Density [g·cm-3]

1.0835

Measurement Temperature [°C]

Rabinowitsch; Zhurnal Fizicheskoi Khimii; vol. 34; (1960); p. 423,424,425; engl.Ausg.; p. 198, View in Reaxys 55 of 98

Density [g·cm-3]

1.0974

Measurement Temperature [°C]

Rabinowitsch; Zhurnal Fizicheskoi Khimii; vol. 34; (1960); p. 423,424,425; engl.Ausg.; p. 198, View in Reaxys 56 of 98

Density [g·cm-3]

1.111

Measurement Temperature [°C]

Rabinowitsch; Zhurnal Fizicheskoi Khimii; vol. 34; (1960); p. 423,424,425; engl.Ausg.; p. 198, View in Reaxys 57 of 98

Density [g·cm-3]

1.1245

Measurement Temperature [°C]

Rabinowitsch; Zhurnal Fizicheskoi Khimii; vol. 34; (1960); p. 423,424,425; engl.Ausg.; p. 198, View in Reaxys 58 of 98

Density [g·cm-3]

1.1379

Measurement Temperature [°C]

Rabinowitsch; Zhurnal Fizicheskoi Khimii; vol. 34; (1960); p. 423,424,425; engl.Ausg.; p. 198, View in Reaxys 59 of 98

Density [g·cm-3]

1.13816

Reference Temperature [°C]

Measurement Temperature [°C]

Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys 60 of 98

Density [g·cm-3]

1.13128

Reference Temperature [°C]

Measurement Temperature [°C]

Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys 61 of 98

Density [g·cm-3]

1.12439

Reference Temperature [°C]

Measurement Temperature [°C]

Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys 62 of 98

Density [g·cm-3]

1.138

33/412

2016-04-19 03:35:30

Measurement Temperature [°C]

Kotisek; Marek; Chemicky Prumysl; vol. 5; (1955); p. 330,331, 332; Chem.Abstr.; nb. 6239; (1960), View in Reaxys 63 of 98

Density [g·cm-3]

1.13749

Reference Temperature [°C]

Measurement Temperature [°C]

Thompson et al.; Journal of the American Chemical Society; vol. 76; (1954); p. 3445, View in Reaxys 64 of 98

Density [g·cm-3]

1.13064

Reference Temperature [°C]

Measurement Temperature [°C]

Thompson et al.; Journal of the American Chemical Society; vol. 76; (1954); p. 3445, View in Reaxys 65 of 98

Density [g·cm-3]

1.12398

Reference Temperature [°C]

Measurement Temperature [°C]

Thompson et al.; Journal of the American Chemical Society; vol. 76; (1954); p. 3445, View in Reaxys 66 of 98

Density [g·cm-3]

0.1302

Reference Temperature [°C]

Measurement Temperature [°C]

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys 67 of 98

Density [g·cm-3]

1.1235

Reference Temperature [°C]

Measurement Temperature [°C]

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys 68 of 98

Comment (Density)

Density:Dichte des Dampfes bei 760 Torr und Temperaturen von 107grad (2.015 g*lE-1) bis 166.5grad (1.704 g*lE-1).

Corelli; Annali di Chimica Applicata; vol. 39; (1949); p. 591,596, View in Reaxys 69 of 98

Density [g·cm-3]

1.0815 - 1.1371

Reference Temperature [°C]

Measurement Temperature [°C]

20 - 60.9

Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys 70 of 98

Density [g·cm-3]

1.0318 - 1.1416

Reference Temperature [°C]

Measurement Temperature [°C]

16.4 - 96.3

Friend; Hargreaves; Phil.Mag.; vol. <7>34; (1943); p. 814; Chem.Abstr.; (1944); p. 1409, View in Reaxys 71 of 98

Density [g·cm-3]

1.1312

34/412

2016-04-19 03:35:30

Reference Temperature [°C]

Measurement Temperature [°C]

Groves; Sugden; Journal of the Chemical Society; (1937); p. 162, View in Reaxys; Wright; Murray-Rust; Hartley; Journal of the Chemical Society; (1931); p. 202, View in Reaxys; Boyd; Copeland; Journal of the American Chemical Society; vol. 64; (1942); p. 2542, View in Reaxys 72 of 98

Density [g·cm-3]

1.1371

Reference Temperature [°C]

Measurement Temperature [°C]

Suhrmann; Klein; Zeitschrift fuer Physikalische Chemie, Abteilung B: Chemie der Elementarprozesse, Aufbau der Materie; vol. 50; (1941); p. 50, View in Reaxys 73 of 98

Density [g·cm-3]

1.1314

Reference Temperature [°C]

Measurement Temperature [°C]

Smyth; Walls; Journal of Chemical Physics; vol. 3; (1935); p. 557, View in Reaxys 74 of 98

Density [g·cm-3]

1.16405

Reference Temperature [°C]

Measurement Temperature [°C]

Walden; Birr; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 163; (1933); p. 273,335, View in Reaxys 75 of 98

Density [g·cm-3]

1.13149

Reference Temperature [°C]

Measurement Temperature [°C]

Walden; Birr; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 163; (1933); p. 273,335, View in Reaxys 76 of 98

Density [g·cm-3]

1.09792

Reference Temperature [°C]

Measurement Temperature [°C]

Walden; Birr; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 163; (1933); p. 273,335, View in Reaxys 77 of 98

Density [g·cm-3]

1.1649

Reference Temperature [°C]

Measurement Temperature [°C]

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 558, View in Reaxys 78 of 98

Density [g·cm-3]

1.14476

Reference Temperature [°C]

35/412

2016-04-19 03:35:30

Measurement Temperature [°C]

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 558, View in Reaxys 79 of 98

Density [g·cm-3]

1.12453

Reference Temperature [°C]

Measurement Temperature [°C]

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 558, View in Reaxys 80 of 98

Density [g·cm-3]

1.1398

Reference Temperature [°C]

Measurement Temperature [°C]

Hebeisen; Annalen der Physik (Weinheim, Germany); vol. <4> 77; (1925); p. 217, View in Reaxys 81 of 98

Density [g·cm-3]

1.1399

Reference Temperature [°C]

Measurement Temperature [°C]

Eisele; Annalen der Physik (Weinheim, Germany); vol. <4> 76; (1925); p. 400, View in Reaxys 82 of 98

Density [g·cm-3]

1.132

Reference Temperature [°C]

Measurement Temperature [°C]

Williams; Journal of the American Chemical Society; vol. 47; (1925); p. 2646, View in Reaxys 83 of 98

Density [g·cm-3]

1.1322

Reference Temperature [°C]

Measurement Temperature [°C]

Williams; Journal of the American Chemical Society; vol. 47; (1925); p. 2646, View in Reaxys 84 of 98

Density [g·cm-3]

1.1654 - 1.0164

Measurement Temperature [°C]

0 - 85

Philip; Oakley; Journal of the Chemical Society; vol. 125; (1924); p. 1194, View in Reaxys 85 of 98

Density [g·cm-3]

1.1385

Measurement Temperature [°C]

Harkins; Clark; Roberts; Journal of the American Chemical Society; vol. 42; (1920); p. 703, View in Reaxys 86 of 98

Density [g·cm-3]

1.097

Reference Temperature [°C]

Measurement Temperature [°C]

Jaeger; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 101; (1917); p. 66, View in Reaxys

36/412

2016-04-19 03:35:30

87 of 98

Density [g·cm-3]

1.1297

Reference Temperature [°C]

Measurement Temperature [°C]

Jaeger; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 101; (1917); p. 66, View in Reaxys 88 of 98

Density [g·cm-3]

1.1437

Reference Temperature [°C]

Measurement Temperature [°C]

Jaeger; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 101; (1917); p. 66, View in Reaxys 89 of 98

Comment (Density)

Density:Dt:1.1639(1-0.001152t).

Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 65; (1909); p. 134; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 66; (1909); p. 395,427, View in Reaxys 90 of 98

Density [g·cm-3]

1.1639

Reference Temperature [°C]

Measurement Temperature [°C]

Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 55; (1906); p. 220, View in Reaxys 91 of 98

Density [g·cm-3]

1.1307

Reference Temperature [°C]

Measurement Temperature [°C]

Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 55; (1906); p. 220, View in Reaxys 92 of 98

Density [g·cm-3]

1.1354

Reference Temperature [°C]

Measurement Temperature [°C]

21.6

Bruehl; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 16; (1895); p. 214; Chemische Berichte; vol. 26; (1893); p. 2515, View in Reaxys 93 of 98

Density [g·cm-3]

1.158

Reference Temperature [°C]

Measurement Temperature [°C]

Perkin; Journal of the Chemical Society; vol. 55; (1889); p. 748, View in Reaxys 94 of 98

Density [g·cm-3]

1.1502

Reference Temperature [°C]

Measurement Temperature [°C]

Perkin; Journal of the Chemical Society; vol. 55; (1889); p. 748, View in Reaxys 95 of 98

Density [g·cm-3]

1.1441

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Reference Temperature [°C]

Measurement Temperature [°C]

Perkin; Journal of the Chemical Society; vol. 55; (1889); p. 748, View in Reaxys 96 of 98

Density [g·cm-3]

1.1382

Reference Temperature [°C]

Measurement Temperature [°C]

Perkin; Journal of the Chemical Society; vol. 55; (1889); p. 748, View in Reaxys 97 of 98

Density [g·cm-3]

1.133

Reference Temperature [°C]

Measurement Temperature [°C]

Perkin; Journal of the Chemical Society; vol. 55; (1889); p. 748, View in Reaxys 98 of 98

Density [g·cm-3]

1.0236

Reference Temperature [°C]

Measurement Temperature [°C]

101

Schiff,R.; Chemische Berichte; vol. 19; (1886); p. 567, View in Reaxys Adsorption (MCS) (67) 1 of 67

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

glycine-glycine-glycine

Ziganshin, Marat A.; Ziganshina, Sufia A.; Gubina, Nadezhda S.; Gerasimov, Alexander V.; Gorbatchuk, Valery V.; Bukharaev, Anastas A.; Oriental Journal of Chemistry; vol. 31; nb. 4; (2015); p. 1977 - 1984, View in Reaxys 2 of 67

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

glycylglycine

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

129.84

Partner (Adsorption (MCS))

silicas

Roshchina; Shoniya; Lagutova; Fadeev; Russian Journal of Physical Chemistry A; vol. 82; nb. 3; (2008); p. 390 396, View in Reaxys 4 of 67

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

129.84

Partner (Adsorption (MCS))

silicas grafted -Si(-CH3)2-(CH2)3-(n-C6F13)

38/412

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Roshchina; Shoniya; Lagutova; Fadeev; Russian Journal of Physical Chemistry A; vol. 82; nb. 3; (2008); p. 390 396, View in Reaxys 5 of 67

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

129.84

Partner (Adsorption (MCS))

silicas grafted =Si(-CH3)-(CH2)2-(n-C6F13)

Roshchina; Shoniya; Lagutova; Fadeev; Russian Journal of Physical Chemistry A; vol. 82; nb. 3; (2008); p. 390 396, View in Reaxys 6 of 67

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

129.84

Partner (Adsorption (MCS))

silicas grafted <*>Si-(CH2)2-(n-C6F13)

Roshchina; Shoniya; Lagutova; Fadeev; Russian Journal of Physical Chemistry A; vol. 82; nb. 3; (2008); p. 390 396, View in Reaxys 7 of 67

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

129.84

Partner (Adsorption (MCS))

silicas grafted -Si(-CH3)-(n-C8H17)

Roshchina; Shoniya; Lagutova; Fadeev; Russian Journal of Physical Chemistry A; vol. 82; nb. 3; (2008); p. 390 396, View in Reaxys 8 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

polystyrene, supercross-linked

Bardina; Zhukova; Kovaleva; Lanin; Russian Journal of Physical Chemistry A; vol. 81; nb. 9; (2007); p. 1525 1531, View in Reaxys 9 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

poly(styrene-co-divinylbenzene)

Bardina; Zhukova; Kovaleva; Lanin; Russian Journal of Physical Chemistry A; vol. 81; nb. 9; (2007); p. 1525 1531, View in Reaxys 10 of 67

Description (Adsorption (MCS))

Adsorption isotherm

Temperature (Adsorption (MCS)) [°C]

100

Partner (Adsorption (MCS))

KSKG silica gel (GOST 3956-76)

Kovaleva; Lanin; Samadani Langerudi; Russian Journal of Physical Chemistry A; vol. 80; nb. 6; (2006); p. 945 949, View in Reaxys 11 of 67

Description (Adsorption (MCS))

Desorption

Temperature (Adsorption (MCS)) [°C]

26.85 - 756.85

Partner (Adsorption (MCS))

Mg-Al hydrotalciteRL500

39/412

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Abello; Medina; Tichit; Perez-Ramirez; Cesteros; Salagre; Sueiras; Chemical Communications; nb. 11; (2005); p. 1453 - 1455, View in Reaxys 12 of 67

Description (Adsorption (MCS))

Desorption

Temperature (Adsorption (MCS)) [°C]

26.85 - 756.85

Partner (Adsorption (MCS))

Mg-Al hydrotalciteRG

Abello; Medina; Tichit; Perez-Ramirez; Cesteros; Salagre; Sueiras; Chemical Communications; nb. 11; (2005); p. 1453 - 1455, View in Reaxys 13 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

PEG-modified silica gel

Bardina; Kovaleva; Nikitin; Russian Journal of Physical Chemistry A; vol. 75; nb. 3; (2001); p. 442 - 445, View in Reaxys 14 of 67

Description (Adsorption (MCS))

Adsorption

Comment (Adsorption (MCS))

ambient temperature

Partner (Adsorption (MCS))

H-ZSM-5

Kevan; Park; Cho; Physical Chemistry Chemical Physics; vol. 3; nb. 15; (2001); p. 3247 - 3253, View in Reaxys 15 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

Polysorb-1

Shepelenko; Zibarev; Russian Journal of Physical Chemistry A; vol. 75; nb. 8; (2001); p. 1351 - 1354, View in Reaxys 16 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Temperature (Adsorption (MCS)) [°C]

100 - 150

Partner (Adsorption (MCS))

silochrom S-120 macroporous silica

Bardina; Kovaleva; Nikitin; Russian Journal of Physical Chemistry A; vol. 74; nb. 3; (2000); p. 421 - 425, View in Reaxys 17 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Temperature (Adsorption (MCS)) [°C]

100

Partner (Adsorption (MCS))

hexadecyl-modified silica

Roshchina; Astakhov; Gurevich; Lisichkin; Russian Journal of Physical Chemistry A; vol. 74; nb. 10; (2000); p. 1670 - 1674, View in Reaxys 18 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Temperature (Adsorption (MCS)) [°C]

100

Partner (Adsorption (MCS))

polyfluoroalkyl-modified silica

Roshchina; Astakhov; Gurevich; Lisichkin; Russian Journal of Physical Chemistry A; vol. 74; nb. 10; (2000); p. 1670 - 1674, View in Reaxys

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19 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Temperature (Adsorption (MCS)) [°C]

100

Partner (Adsorption (MCS))

teflon-4

Roshchina; Astakhov; Gurevich; Lisichkin; Russian Journal of Physical Chemistry A; vol. 74; nb. 10; (2000); p. 1670 - 1674, View in Reaxys 20 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

lignosulfonate H-form

Makarevich; Afanas'ev; Telysheva; Monakov; Russian Journal of Physical Chemistry A; vol. 74; nb. 12; (2000); p. 2001 - 2007, View in Reaxys 21 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

lignosulfonate NH4-form

Makarevich; Afanas'ev; Telysheva; Monakov; Russian Journal of Physical Chemistry A; vol. 74; nb. 12; (2000); p. 2001 - 2007, View in Reaxys 22 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

lignosulfonate K-form

Makarevich; Afanas'ev; Telysheva; Monakov; Russian Journal of Physical Chemistry A; vol. 74; nb. 12; (2000); p. 2001 - 2007, View in Reaxys 23 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

lignosulfonate Na-form

Makarevich; Afanas'ev; Telysheva; Monakov; Russian Journal of Physical Chemistry A; vol. 74; nb. 12; (2000); p. 2001 - 2007, View in Reaxys 24 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

lignosulfonate Li-form

Makarevich; Afanas'ev; Telysheva; Monakov; Russian Journal of Physical Chemistry A; vol. 74; nb. 12; (2000); p. 2001 - 2007, View in Reaxys 25 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

technical lignosulfonate

Makarevich; Afanas'ev; Telysheva; Monakov; Russian Journal of Physical Chemistry A; vol. 74; nb. 12; (2000); p. 2001 - 2007, View in Reaxys 26 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

fractionated lignosulfonate, mean molecular weight 24000

Makarevich; Afanas'ev; Telysheva; Monakov; Russian Journal of Physical Chemistry A; vol. 74; nb. 12; (2000); p. 2001 - 2007, View in Reaxys 27 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

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Partner (Adsorption (MCS))

fractionated lignosulfonate, mean molecular weight 32500

Makarevich; Afanas'ev; Telysheva; Monakov; Russian Journal of Physical Chemistry A; vol. 74; nb. 12; (2000); p. 2001 - 2007, View in Reaxys 28 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

fractionated lignosulfonate, mean molecular weight 57000

Makarevich; Afanas'ev; Telysheva; Monakov; Russian Journal of Physical Chemistry A; vol. 74; nb. 12; (2000); p. 2001 - 2007, View in Reaxys 29 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

silica

Roshchina; Shoniya; Kitaev; Gurevich; Kaz'mina; Russian Journal of Physical Chemistry A; vol. 74; nb. 12; (2000); p. 2026 - 2033, View in Reaxys 30 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

phenyltrichlorosilane and (CH3)2NSi(CH3)3 modified silica

Roshchina; Shoniya; Kitaev; Gurevich; Kaz'mina; Russian Journal of Physical Chemistry A; vol. 74; nb. 12; (2000); p. 2026 - 2033, View in Reaxys 31 of 67

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

SnO2

Bardina; Gas'kov; Kovaleva; Kudryavtseva; Nikitin; Russian Journal of Physical Chemistry A; vol. 73; nb. 1; (1999); p. 101 - 105, View in Reaxys 32 of 67

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Partner (Adsorption (MCS))

SnO2

Bardina; Gas'kov; Kovaleva; Kudryavtseva; Nikitin; Russian Journal of Physical Chemistry A; vol. 73; nb. 1; (1999); p. 101 - 105, View in Reaxys 33 of 67

Description (Adsorption (MCS))

Adsorption isotherm

Temperature (Adsorption (MCS)) [°C]

24.9

Partner (Adsorption (MCS))

human serum albumin

Gorbatchuk, Valery V.; Ziganshin, Marat A.; Solomonov, Boris N.; Borisover, Mikhail D.; Journal of Physical Organic Chemistry; vol. 10; nb. 12; (1997); p. 901 - 907, View in Reaxys 34 of 67

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

-173.1 - 26.9

Partner (Adsorption (MCS))

polycrystalline Pt

Levoguer; Nix; Journal of the Chemical Society - Faraday Transactions; vol. 93; nb. 9; (1997); p. 1813 - 1820, View in Reaxys 35 of 67

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

42/412

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Temperature (Adsorption (MCS)) [°C]

-173.1 - 26.9

Partner (Adsorption (MCS))

polycrystalline Pt

Levoguer; Nix; Journal of the Chemical Society - Faraday Transactions; vol. 93; nb. 9; (1997); p. 1813 - 1820, View in Reaxys 36 of 67

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Partner (Adsorption (MCS))

γ-alumina

Yamaguchi, Makoto; Journal of the Chemical Society - Faraday Transactions; vol. 93; nb. 19; (1997); p. 3581 3586, View in Reaxys 37 of 67

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

150

Partner (Adsorption (MCS))

silica, modified silicas (aminated, glucose treated)

Dernovaya; El'tekov; Russian Journal of Physical Chemistry A; vol. 70; nb. 4; (1996); p. 677 - 681, View in Reaxys 38 of 67

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Temperature (Adsorption (MCS)) [°C]

100

Partner (Adsorption (MCS))

carbopak C HT

Davydov; Roshchina; Filatova; Khrustaleva; Russian Journal of Physical Chemistry A; vol. 70; nb. 10; (1996); p. 1723 - 1728, View in Reaxys 39 of 67

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

carbon adsorbent

Belyakova, L. D.; Voloschchuk, A. M.; Vorob'eva, L. M.; Larionova, A. O.; Larionov, O. G.; Russian Journal of Physical Chemistry; vol. 69; nb. 3; (1995); p. 455 - 459; Zhurnal Fizicheskoi Khimii; vol. 69; nb. 3; (1995); p. 501 505, View in Reaxys 40 of 67

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

20 - 150

Partner (Adsorption (MCS))

Styrosorb specimen 1

Belyakova, L. D.; Vasilevskaya, O. V.; Tsyurupa, M. P.; Davankov, V. A.; Russian Journal of Physical Chemistry; vol. 69; nb. 4; (1995); p. 631 - 635; Zhurnal Fizicheskoi Khimii; vol. 69; nb. 4; (1995); p. 696 - 700, View in Reaxys 41 of 67

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

20 - 150

Partner (Adsorption (MCS))

Styrosorb specimen 2

Description (Adsorption (MCS))

Enthalpy of adsorption

43/412

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Temperature (Adsorption (MCS)) [°C]

35 - 75

Partner (Adsorption (MCS))

carbon fibers (SOFICAR, T-300)

Park, S. J.; Papirer, E.; Donnet, J. B.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 91; nb. 2; (1994); p. 203 - 222, View in Reaxys 43 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

1-aminooctadecane; γ-Fe2O3

Dernovaya, L. I.; Chalykh, A. E.; El'tekov, Yu. A.; Russian Journal of Physical Chemistry; vol. 67; nb. 10; (1993); p. 1796 - 1799; Zhurnal Fizicheskoi Khimii; vol. 67; nb. 10; (1993); p. 1966 - 2000, View in Reaxys 44 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Partner (Adsorption (MCS))

n-octadecanoic acid; γ-Fe2O3

Description (Adsorption (MCS))

Chemisorption

Solvent (Adsorption (MCS))

H2O; various solvent(s)

Partner (Adsorption (MCS))

Fe2O3/SiO2

Nikolenko, N. V.; Kholodkova, O. V.; Kuprin, V. P.; Davidenko, A. N.; Plaksienko, I. L.; J. Appl. Chem. USSR (Engl. Transl.); vol. 64; nb. 10.2; (1991); p. 2162 - 2165,2022 - 2024, View in Reaxys 46 of 67

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

hexanoic acid

Abramzon, A. A.; Grigor'ev, S. N.; Makagonova, N. N.; Russian Journal of Physical Chemistry; vol. 65; nb. 4; (1991); p. 525 - 528; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p. 1001 - 1007, View in Reaxys 47 of 67

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Partner (Adsorption (MCS))

poly(4-vinylpyridine)

Korb, J.-P.; Sapoval, B.; Chachaty, C.; Tistchenko, A.M.; Journal of Physical Chemistry; vol. 94; nb. 2; (1990); p. 953 - 958, View in Reaxys 48 of 67

Description (Adsorption (MCS))

Desorption

Temperature (Adsorption (MCS)) [°C]

26.9 - 826.9

Partner (Adsorption (MCS))

clean Rh(111) surface

Hwang, S. Y.; Kong, A. C. F.; Schmidt, L. D.; Journal of Physical Chemistry; vol. 93; nb. 26; (1989); p. 8334 8343, View in Reaxys 49 of 67

Description (Adsorption (MCS))

Desorption

Temperature (Adsorption (MCS)) [°C]

26.9 - 826.9

Partner (Adsorption (MCS))

clean Pt(111) surface

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Hwang, S. Y.; Kong, A. C. F.; Schmidt, L. D.; Journal of Physical Chemistry; vol. 93; nb. 26; (1989); p. 8334 8343, View in Reaxys 50 of 67

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Temperature (Adsorption (MCS)) [°C]

100

Partner (Adsorption (MCS))

graphitised black

Reznikov, S. A.; Sidorov, R. I.; Russian Journal of Physical Chemistry; vol. 62; nb. 11; (1988); p. 1612 - 1613; Zhurnal Fizicheskoi Khimii; vol. 62; (1988); p. 3089 - 3091, View in Reaxys 51 of 67

Description (Adsorption (MCS))

Adsorption isotherm

Solvent (Adsorption (MCS))

methanol; H2O

Partner (Adsorption (MCS))

alkylated silica gel

Guglya, E. B.; Yanovskii, S. M.; Russian Journal of Physical Chemistry; vol. 60; nb. 12; (1986); p. 1846 - 1849; Zhurnal Fizicheskoi Khimii; vol. 60; (1986); p. 3069 - 3073, View in Reaxys 52 of 67

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Temperature (Adsorption (MCS)) [°C]

22.1

Partner (Adsorption (MCS))

methyl cyclohexane

Pyzuk, Wieslaw; Krupkowski, Teodor; Dolecki, Jerzy; Paduszek, Barbara; Polish Journal of Chemistry; vol. 56; nb. 10-12; (1982); p. 1477 - 1482, View in Reaxys 53 of 67

Description (Adsorption (MCS))

Adsorption isotherm

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

ZnO

Nagao, Mahiko; Matsuoka, Kazuyuki; Hirai, Hitoko; Morimoto, Tetsuo; Journal of Physical Chemistry; vol. 86; nb. 21; (1982); p. 4188 - 4193, View in Reaxys 54 of 67

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Partner (Adsorption (MCS))

ZnO

Nagao, Mahiko; Matsuoka, Kazuyuki; Hirai, Hitoko; Morimoto, Tetsuo; Journal of Physical Chemistry; vol. 86; nb. 21; (1982); p. 4188 - 4193, View in Reaxys 55 of 67

Description (Adsorption (MCS))

Adsorption

Revcroft et al.; Journal of Physical Chemistry; vol. 75; (1971); p. 3526, View in Reaxys; Bottomley et al.; Australian Journal of Chemistry; vol. 18; (1965); p. 1105, View in Reaxys; Radaev; Glushchenko; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 22; (1973); p. 2268; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 22; (1973); p. 2327, View in Reaxys; Davydov et al.; Russian Journal of Physical Chemistry; vol. 39; (1965); p. 1096; Zhurnal Fizicheskoi Khimii; p. 2058, View in Reaxys; Staudte; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 255; (1974); p. 158,160, View in Reaxys; Barrer; Locke; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 40; (1964); p. 301,304, View in Reaxys; Avramenko et al.; Russian Journal of Physical Chemistry; vol. 49; (1975); p. 902; ; p. 1532, View in Reaxys 56 of 67

Description (Adsorption (MCS))

Adsorption isotherm

Revcroft et al.; Journal of Physical Chemistry; vol. 75; (1971); p. 3526, View in Reaxys; Avramenko et al.; Russian Journal of Physical Chemistry; vol. 49; (1975); p. 902; ; p. 1532, View in Reaxys

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57 of 67

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Kiselev; Discussions of the Faraday Society; vol. 52; (1971); p. 14, View in Reaxys 58 of 67

Description (Adsorption (MCS))

Enthalpy of adsorption

Kiselev et al.; Russian Journal of Physical Chemistry; vol. 42; (1968); p. 644; ; p. 1235, View in Reaxys 59 of 67

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

tetrachloromethane; silica gel

Jones; Mill; Journal of the Chemical Society; (1957); p. 213, View in Reaxys 60 of 67

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

benzene; silica gel

Jones; Mill; Journal of the Chemical Society; (1957); p. 213, View in Reaxys 61 of 67

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

nitrobenzene; silica gel

Jones; Mill; Journal of the Chemical Society; (1957); p. 213, View in Reaxys 62 of 67

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

polystyrene film

Burrage; Transactions of the Faraday Society; vol. 44; p. 498; Chem.Abstr.; (1949); p. 437, View in Reaxys 63 of 67

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

montmorillonite

MacEwan; Transactions of the Faraday Society; vol. 44; (1948); p. 356; Chem.Abstr.; (1949); p. 463, View in Reaxys 64 of 67

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

halloysite

MacEwan; Transactions of the Faraday Society; vol. 44; (1948); p. 356; Chem.Abstr.; (1949); p. 463, View in Reaxys 65 of 67

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

cyclohexane

Partner (Adsorption (MCS))

wood coal

Lessochina; Golbert; Shuchowitzki; Zhurnal Fizicheskoi Khimii; vol. 22; (1948); p. 968,969; Chem.Abstr.; (1949); p. 461, View in Reaxys 66 of 67

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

non-activated coal

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Burrage; Transactions of the Faraday Society; vol. 29; (1933); p. 462; Transactions of the Faraday Society; vol. 30; (1934); p. 318, View in Reaxys 67 of 67

Description (Adsorption (MCS))

Adsorption

Comment (Adsorption (MCS))

des Dampfes.

Partner (Adsorption (MCS))

mercury

Cassel; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 37; (1931); p. 643, View in Reaxys Association (MCS) (168) 1 of 168

Description (Association IR spectrum of the complex (MCS)) Solvent (Association (MCS))

nujol

Partner (Association (MCS))

(o-C6F4Hg)3

Tikhonova; Tugashov; Dolgushin; Yakovenko; Petrovskii; Furin; Zaraisky; Shur; Journal of Organometallic Chemistry; vol. 692; nb. 5; (2007); p. 953 - 962, View in Reaxys 2 of 168

Description (Association Association with compound (MCS)) Solvent (Association (MCS))

cyclohexane

Temperature (Association (MCS)) [°C]

74.85

Partner (Association (MCS))

styrene

Al-Shawabkeh, Ali F.; Al-Wahab, Haitham A.; Shahab, Yousif A.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 66; nb. 3; (2007); p. 739 - 744, View in Reaxys 3 of 168

Description (Association Association with compound (MCS)) Solvent (Association (MCS))

cyclohexane

Temperature (Association (MCS)) [°C]

74.85

Partner (Association (MCS))

vinyl acetate

Al-Shawabkeh, Ali F.; Al-Wahab, Haitham A.; Shahab, Yousif A.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 66; nb. 3; (2007); p. 739 - 744, View in Reaxys 4 of 168

Description (Association IR spectrum of the complex (MCS)) Partner (Association (MCS))

Ag/Al2O3

Gao, Hongwei; He, Hong; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 61; nb. 6; (2005); p. 1233 - 1238, View in Reaxys 5 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CDCl3

Partner (Association (MCS))

C62H72O6

Rojanathanes, Rojrit; Tuntulani, Thawatchai; Bhanthumnavin, Worawan; Sukwattanasinitt, Mongkol; Organic Letters; vol. 7; nb. 16; (2005); p. 3401 - 3404, View in Reaxys

47/412

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6 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CDCl3

Partner (Association (MCS))

C62H72O6

Rojanathanes, Rojrit; Tuntulani, Thawatchai; Bhanthumnavin, Worawan; Sukwattanasinitt, Mongkol; Organic Letters; vol. 7; nb. 16; (2005); p. 3401 - 3404, View in Reaxys 7 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CDCl3

Partner (Association (MCS))

C62H72O6

Rojanathanes, Rojrit; Tuntulani, Thawatchai; Bhanthumnavin, Worawan; Sukwattanasinitt, Mongkol; Organic Letters; vol. 7; nb. 16; (2005); p. 3401 - 3404, View in Reaxys 8 of 168

Description (Association Association with compound (MCS)) Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

methanol

Vokin; Oznobikhina; Shulunova; Fedorov; Turchaninov; Russian Journal of General Chemistry; vol. 75; nb. 10; (2005); p. 1566 - 1575, View in Reaxys 9 of 168

Description (Association Association with compound (MCS)) Temperature (Association (MCS)) [°C]

Comment (Association (MCS))

film

Partner (Association (MCS))

cycloheptaamylose

Shtykov; Korenman; Rusanova; Gorin; Kalach; Pankin; Doklady Chemistry; vol. 396; nb. 4-6; (2004); p. 119 121, View in Reaxys 10 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CDCl3

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

C102H90O26

Ihm, Hyejae; Hwang, Soo-Jin; Paek, Kyungsoo; Tetrahedron Letters; vol. 45; nb. 49; (2004); p. 9119 - 9122, View in Reaxys 11 of 168

Description (Association Enthalpy of association (MCS)) Partner (Association (MCS))

1,1-diphenylethanol

Sultanly; Akhmedli; Mamedova; Journal of Applied Spectroscopy; vol. 71; nb. 4; (2004); p. 592 - 596, View in Reaxys 12 of 168

Description (Association Enthalpy of association (MCS))

48/412

2016-04-19 03:35:30

Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

5,11,17,23-tetra-tert-butyl-25,27-dihydroxy-26-methyloxycalix[4]arene

Hirakata, Masaki; Yoshimura, Kosaku; Usui, Shuji; Nishimoto, Koji; Fukazawa, Yoshimasa; Tetrahedron Letters; vol. 43; nb. 10; (2002); p. 1859 - 1861, View in Reaxys 13 of 168

Description (Association Association with compound (MCS)) Solvent (Association (MCS))

aq. phosphate buffer

Temperature (Association (MCS)) [°C]

24.85

Comment (Association (MCS))

neutral solution

Partner (Association (MCS))

5,10,15,20-tetra(N-methylpyridinium-4-yl)porphine

Liu, Tianjun; Schneider, Hans-Joerg; Angewandte Chemie - International Edition; vol. 41; nb. 8; (2002); p. 1368 1370, View in Reaxys 14 of 168

Description (Association Association with compound (MCS)) Solvent (Association (MCS))

aq. phosphate buffer

Temperature (Association (MCS)) [°C]

24.85

Comment (Association (MCS))

neutral solution

Partner (Association (MCS))

C44H26N4O12S4(4-)*Na(1+)

Liu, Tianjun; Schneider, Hans-Joerg; Angewandte Chemie - International Edition; vol. 41; nb. 8; (2002); p. 1368 1370, View in Reaxys 15 of 168

Description (Association UV/VIS spectrum of the complex (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

aniline

Muzaffar; Andrabi, Ali; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 41; nb. 11; (2002); p. 2306 - 2309, View in Reaxys 16 of 168

Description (Association UV/VIS spectrum of the complex (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

N-methylaniline

Muzaffar; Andrabi, Ali; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 41; nb. 11; (2002); p. 2306 - 2309, View in Reaxys 17 of 168

Description (Association UV/VIS spectrum of the complex (MCS))

49/412

2016-04-19 03:35:30

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

dimethylaniline

Muzaffar; Andrabi, Ali; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 41; nb. 11; (2002); p. 2306 - 2309, View in Reaxys 18 of 168

Description (Association UV/VIS spectrum of the complex (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

N,N-diethylaniline

Muzaffar; Andrabi, Ali; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 41; nb. 11; (2002); p. 2306 - 2309, View in Reaxys 19 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

aniline

Muzaffar; Andrabi, Ali; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 41; nb. 11; (2002); p. 2306 - 2309, View in Reaxys 20 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

N-methylaniline

Muzaffar; Andrabi, Ali; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 41; nb. 11; (2002); p. 2306 - 2309, View in Reaxys 21 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

dimethylaniline

Muzaffar; Andrabi, Ali; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 41; nb. 11; (2002); p. 2306 - 2309, View in Reaxys 22 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CCl4

50/412

2016-04-19 03:35:30

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

N,N-diethylaniline

Muzaffar; Andrabi, Ali; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 41; nb. 11; (2002); p. 2306 - 2309, View in Reaxys 23 of 168

Description (Association NMR spectrum of the complex (MCS)) Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

aniline

Muzaffar; Andrabi, Ali; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 41; nb. 11; (2002); p. 2306 - 2309, View in Reaxys 24 of 168

Description (Association NMR spectrum of the complex (MCS)) Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

dimethylaniline

Muzaffar; Andrabi, Ali; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 41; nb. 11; (2002); p. 2306 - 2309, View in Reaxys 25 of 168

Description (Association IR spectrum of the complex (MCS)) Partner (Association (MCS))

Mo(110)

Chan, Ally S. Y.; Deiner, L. Jay; Friend; Journal of Physical Chemistry B; vol. 106; nb. 51; (2002); p. 13318 13325, View in Reaxys 26 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CDCl3

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

C78H68O18

Paek, Kyungsoo; Cho, Jooyeon; Tetrahedron Letters; vol. 42; nb. 10; (2001); p. 1927 - 1929, View in Reaxys 27 of 168

Description (Association IR spectrum of the complex (MCS)) Partner (Association (MCS))

H-ZSM-5

Kevan; Park; Cho; Physical Chemistry Chemical Physics; vol. 3; nb. 15; (2001); p. 3247 - 3253, View in Reaxys 28 of 168

Description (Association Association with compound (MCS)) Partner (Association (MCS))

11,17-Dichlor-29-(N-methyl-N-phenyl)amino-14-(p-tolyl)-2,8,10,12,14,16,18,20,26,28,30,31,33,34-tetradecaazahexacyclo[25.3.1.13,7.19,13.115,19.121,25]pentatriaconta-1(31),3,5,7(35),9,11,13(34),15,17,19(33), 21,23,25(32),27,29-pentadecaene

Graubaum; Lutze; Costisella; Advanced Synthesis and Catalysis; vol. 339; nb. 3; (1997); p. 266 - 271, View in Reaxys 29 of 168

Description (Association Association with compound (MCS))

51/412

2016-04-19 03:35:30

Partner (Association (MCS))

C66H68N2O8

Pinkhassik, Evgueni; Stibor, Ivan; Casnati, Alessandro; Ungaro, Rocco; Journal of Organic Chemistry; vol. 62; nb. 25; (1997); p. 8654 - 8659, View in Reaxys 30 of 168

Description (Association IR spectrum of the complex (MCS)) Solvent (Association (MCS))

CH2Cl2

Temperature (Association (MCS)) [°C]

24.9

Partner (Association (MCS))

4-Fluorophenol

Chardin, Aurelie; Laurence, Christian; Berthelot, Michel; Morris, David G.; Bulletin de la Societe Chimique de France; vol. 133; nb. 4; (1996); p. 389 - 393, View in Reaxys 31 of 168

Description (Association IR spectrum of the complex (MCS)) Solvent (Association (MCS))

CH2Cl2

Temperature (Association (MCS)) [°C]

24.9

Partner (Association (MCS))

methanol

Chardin, Aurelie; Laurence, Christian; Berthelot, Michel; Morris, David G.; Bulletin de la Societe Chimique de France; vol. 133; nb. 4; (1996); p. 389 - 393, View in Reaxys 32 of 168

Description (Association Further physical properties of the complex (MCS)) Temperature (Association (MCS)) [°C]

25 - 75

Partner (Association (MCS))

betaine 30

Bosch, Elisabeth; Roses, Marti; Herodes, Koit; Koppel, Ilmar; Leito, Ivo; Koppel, Ivar; Taal, Veiko; Journal of Physical Organic Chemistry; vol. 9; nb. 6; (1996); p. 403 - 410, View in Reaxys 33 of 168

Description (Association Further physical properties of the complex (MCS)) Temperature (Association (MCS)) [°C]

25 - 75

Partner (Association (MCS))

betaine 30; tert-butanol

Description (Association Further physical properties of the complex (MCS)) Temperature (Association (MCS)) [°C]

25 - 75

Partner (Association (MCS))

betaine 30; isopropyl alcohol

Description (Association Further physical properties of the complex (MCS)) Temperature (Association (MCS)) [°C]

15 - 50

52/412

2016-04-19 03:35:30

Partner (Association (MCS))

betaine 30; methanol

Description (Association Further physical properties of the complex (MCS)) Temperature (Association (MCS)) [°C]

25 - 75

Partner (Association (MCS))

betaine 30; H2O

Description (Association Association with compound (MCS)) Partner (Association (MCS))

2,2'-bis(2,7-di-tert-butyl-9-hydroxyfluoren-9-yl)biphenyl

Weber; Wierig; Skobridis; Advanced Synthesis and Catalysis; vol. 338; nb. 6; (1996); p. 553 - 557, View in Reaxys 38 of 168

Description (Association Association with compound (MCS)) Partner (Association (MCS))

9,9'-lt;2,2'-(1,1'-biphenyl)ylenegt;bis(9H-fluoren-9-ol)

Weber; Wierig; Skobridis; Advanced Synthesis and Catalysis; vol. 338; nb. 6; (1996); p. 553 - 557, View in Reaxys 39 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CDCl3

Temperature (Association (MCS)) [°C]

26.9

Partner (Association (MCS))

25,26-27,28-biscrown-3-calixlt;4gt;arene

Arduini, Arturo; McGregor, William M.; Paganuzzi, Daniela; Pochini, Andrea; Secchi, Andrea; Ugozzoli, Franco; Ungaro, Rocco; Journal of the Chemical Society. Perkin Transactions 2; vol. 5; (1996); p. 839 - 846, View in Reaxys 40 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

26.9

Partner (Association (MCS))

25,26-27,28-biscrown-3-calixlt;4gt;arene

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CDCl3

Temperature (Association (MCS)) [°C]

26.9

Partner (Association (MCS))

5,11,17,23-tetrakis(1,1-dimethylethyl)-25,26-27,28-biscrown-3-calixlt;4gt;arene

53/412

2016-04-19 03:35:30

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

26.9

Partner (Association (MCS))

5,11,17,23-tetrakis(1,1-dimethylethyl)-25,26-27,28-biscrown-3-calixlt;4gt;arene

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CDCl3

Temperature (Association (MCS)) [°C]

26.9

Partner (Association (MCS))

5,11,17,23-tetracyclohexyl-25,26-27,28-biscrown-3-calix[4]arene

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

26.9

Partner (Association (MCS))

5,11,17,23-tetracyclohexyl-25,26-27,28-biscrown-3-calix[4]arene

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

26.9

Partner (Association (MCS))

5,11,17,23-tetrakis(1,1-dimethylethyl)-25,26-27,28-biscrown-4-calix[4]arene

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CDCl3

Temperature (Association (MCS)) [°C]

26.9

54/412

2016-04-19 03:35:30

Partner (Association (MCS))

C68H100N4O8*C6H2N3O7(1-)*Na(1+)

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

benzene-d6

Temperature (Association (MCS)) [°C]

24.9

Partner (Association (MCS))

calix[4]pyrrole

Allen, William E.; Gale, Philip A.; Brown, Christopher T.; Lynch, Vincent M.; Sessler, Jonathan L.; Journal of the American Chemical Society; vol. 118; nb. 49; (1996); p. 12471 - 12472, View in Reaxys 48 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

C66H68N2O8

Pinkhassik, Evgueni; Stibor, Ivan; Havlicek, Vladimir; Collection of Czechoslovak Chemical Communications; vol. 61; nb. 8; (1996); p. 1182 - 1190, View in Reaxys 49 of 168

Description (Association IR spectrum of the complex (MCS)) Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

18-crown-6 ether

Belkin; Yarkov; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 52; nb. 11; (1996); p. 1475 - 1478, View in Reaxys 50 of 168

Description (Association IR spectrum of the complex (MCS)) Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

2,3,5,6,8,9,11,12-octahydro-1,4,7,10,13-benzopentaoxacyclopentadecin

Belkin; Yarkov; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 52; nb. 11; (1996); p. 1475 - 1478, View in Reaxys 51 of 168

Description (Association Further physical properties of the complex (MCS)) Partner (Association (MCS))

H2O

Lovas, F. J.; Zobov, N.; Fraser, G. T.; Suenram, R. D.; Journal of Molecular Spectroscopy; vol. 171; nb. 1; (1995); p. 189 - 199, View in Reaxys 52 of 168

Description (Association Further physical properties of the complex (MCS)) Partner (Association (MCS))

HDO

Lovas, F. J.; Zobov, N.; Fraser, G. T.; Suenram, R. D.; Journal of Molecular Spectroscopy; vol. 171; nb. 1; (1995); p. 189 - 199, View in Reaxys 53 of 168

Description (Association Further physical properties of the complex (MCS))

55/412

2016-04-19 03:35:30

Partner (Association (MCS))

D2O

Lovas, F. J.; Zobov, N.; Fraser, G. T.; Suenram, R. D.; Journal of Molecular Spectroscopy; vol. 171; nb. 1; (1995); p. 189 - 199, View in Reaxys 54 of 168

Description (Association Dipole moment of the complex (MCS)) Partner (Association (MCS))

H2O

Lovas, F. J.; Zobov, N.; Fraser, G. T.; Suenram, R. D.; Journal of Molecular Spectroscopy; vol. 171; nb. 1; (1995); p. 189 - 199, View in Reaxys 55 of 168

Description (Association IR spectrum of the complex (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

methanol

Hong, Xiaoyu; Chen, Sheah; Dlott, Dana D.; Journal of Physical Chemistry; vol. 99; nb. 22; (1995); p. 9102 9109, View in Reaxys 56 of 168

Description (Association IR spectrum of the complex (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

tert-butanol

Hong, Xiaoyu; Chen, Sheah; Dlott, Dana D.; Journal of Physical Chemistry; vol. 99; nb. 22; (1995); p. 9102 9109, View in Reaxys 57 of 168

Description (Association IR spectrum of the complex (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

ethanol

Hong, Xiaoyu; Chen, Sheah; Dlott, Dana D.; Journal of Physical Chemistry; vol. 99; nb. 22; (1995); p. 9102 9109, View in Reaxys 58 of 168

Description (Association IR spectrum of the complex (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

MeOD-d4

Hong, Xiaoyu; Chen, Sheah; Dlott, Dana D.; Journal of Physical Chemistry; vol. 99; nb. 22; (1995); p. 9102 9109, View in Reaxys 59 of 168

Description (Association IR spectrum of the complex (MCS))

56/412

2016-04-19 03:35:30

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

CD3NO2

Hong, Xiaoyu; Chen, Sheah; Dlott, Dana D.; Journal of Physical Chemistry; vol. 99; nb. 22; (1995); p. 9102 9109, View in Reaxys 60 of 168

Description (Association Further physical properties of the complex (MCS)) Temperature (Association (MCS)) [°C]

5 - 45

Partner (Association (MCS))

acetonitrile

D'Aprano, A.; Capalbi, A.; Iammarino, M.; Mauro, V.; Princi, A.; Sesta, B.; Journal of Solution Chemistry; vol. 24; nb. 3; (1995); p. 227 - 240, View in Reaxys 61 of 168

Description (Association Association with compound (MCS)) Temperature (Association (MCS)) [°C]

5 - 45

Partner (Association (MCS))

acetonitrile

D'Aprano, A.; Capalbi, A.; Iammarino, M.; Mauro, V.; Princi, A.; Sesta, B.; Journal of Solution Chemistry; vol. 24; nb. 3; (1995); p. 227 - 240, View in Reaxys 62 of 168

Description (Association Association with compound (MCS)) Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

propylene Carbonate; tetra-n-butylammonium perchlorate

Wawrzyniak, G.; Warnke, Z.; Polish Journal of Chemistry; vol. 68; nb. 4; (1994); p. 817 - 824, View in Reaxys 63 of 168

Description (Association Association with compound (MCS)) Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

propylene Carbonate; tetrabutylammomium bromide

Wawrzyniak, G.; Warnke, Z.; Polish Journal of Chemistry; vol. 68; nb. 4; (1994); p. 817 - 824, View in Reaxys 64 of 168

Description (Association Association with compound (MCS)) Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

propylene Carbonate; tetra-(n-butyl)ammonium iodide

Wawrzyniak, G.; Warnke, Z.; Polish Journal of Chemistry; vol. 68; nb. 4; (1994); p. 817 - 824, View in Reaxys 65 of 168

Description (Association Association with compound (MCS)) Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

propylene Carbonate; N(Et)4ClO4

Wawrzyniak, G.; Warnke, Z.; Polish Journal of Chemistry; vol. 68; nb. 4; (1994); p. 817 - 824, View in Reaxys

57/412

2016-04-19 03:35:30

66 of 168

Description (Association Association with compound (MCS)) Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

propylene Carbonate; tetraethylammonium chloride

Wawrzyniak, G.; Warnke, Z.; Polish Journal of Chemistry; vol. 68; nb. 4; (1994); p. 817 - 824, View in Reaxys 67 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

4-Fluorophenol

Laurence, Christian; Berthelot, Michel; Lucon, Maryvonne; Morris, David G.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 3; (1994); p. 491 - 494, View in Reaxys 68 of 168

Description (Association UV/VIS spectrum of the complex (MCS)) Partner (Association (MCS))

ethylenediamine

Constantinou, C. P.; Winey, J. M.; Gupta, Y. M.; Journal of Physical Chemistry; vol. 98; nb. 32; (1994); p. 7767 7776, View in Reaxys 69 of 168

Description (Association Association with compound (MCS)) Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

propan-1-ol

Bittrich, H.-J.; Eckert, R.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 185; nb. 2; (1994); p. 207 - 222, View in Reaxys 70 of 168

Description (Association Further physical properties of the complex (MCS)) Solvent (Association (MCS))

neat (no solvent)

Temperature (Association (MCS)) [°C]

24.9

Partner (Association (MCS))

CD3NO2

Hill, J. R.; Moore, D. S.; Schmidt, S. C.; Storm, C. B.; Journal of Physical Chemistry; vol. 95; nb. 8; (1991); p. 3037 - 3044, View in Reaxys 71 of 168

Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

29.9

Partner (Association (MCS))

4-nitrophenol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Gonchar, N. P.; Journal of Molecular Structure; vol. 219; (1990); p. 257 - 262, View in Reaxys 72 of 168

Description (Association Stability constant of the complex with ... (MCS))

58/412

2016-04-19 03:35:30

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

29.9

Partner (Association (MCS))

4-nitrophenol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Gonchar, N. P.; Journal of Molecular Structure; vol. 219; (1990); p. 257 - 262, View in Reaxys 73 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

29.9

Partner (Association (MCS))

pyridine; 4-nitrophenol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Gonchar, N. P.; Journal of Molecular Structure; vol. 219; (1990); p. 257 - 262, View in Reaxys 74 of 168

Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

29.9

Partner (Association (MCS))

pyridine; 4-nitrophenol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Gonchar, N. P.; Journal of Molecular Structure; vol. 219; (1990); p. 257 - 262, View in Reaxys 75 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

29.9

Partner (Association (MCS))

3-monochlorophenol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Gonchar, N. P.; Journal of Molecular Structure; vol. 219; (1990); p. 257 - 262, View in Reaxys 76 of 168

Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

29.9

Partner (Association (MCS))

3-monochlorophenol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Gonchar, N. P.; Journal of Molecular Structure; vol. 219; (1990); p. 257 - 262, View in Reaxys 77 of 168

Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

CCl4

59/412

2016-04-19 03:35:30

Temperature (Association (MCS)) [°C]

29.9

Partner (Association (MCS))

4-chlorophenol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Gonchar, N. P.; Journal of Molecular Structure; vol. 219; (1990); p. 257 - 262, View in Reaxys 78 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

29.9

Partner (Association (MCS))

4-chlorophenol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Gonchar, N. P.; Journal of Molecular Structure; vol. 219; (1990); p. 257 - 262, View in Reaxys 79 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

29.9

Partner (Association (MCS))

phenol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Gonchar, N. P.; Journal of Molecular Structure; vol. 219; (1990); p. 257 - 262, View in Reaxys 80 of 168

Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

29.9

Partner (Association (MCS))

phenol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Gonchar, N. P.; Journal of Molecular Structure; vol. 219; (1990); p. 257 - 262, View in Reaxys 81 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

29.9

Partner (Association (MCS))

pyridine; phenol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Gonchar, N. P.; Journal of Molecular Structure; vol. 219; (1990); p. 257 - 262, View in Reaxys 82 of 168

Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

29.9

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Partner (Association (MCS))

pyridine; phenol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Gonchar, N. P.; Journal of Molecular Structure; vol. 219; (1990); p. 257 - 262, View in Reaxys 83 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CH2Cl2

Temperature (Association (MCS)) [°C]

29.9

Partner (Association (MCS))

acetonitrile; phenol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Gonchar, N. P.; Journal of Molecular Structure; vol. 219; (1990); p. 257 - 262, View in Reaxys 84 of 168

Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

CH2Cl2

Temperature (Association (MCS)) [°C]

29.9

Partner (Association (MCS))

acetonitrile; phenol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Gonchar, N. P.; Journal of Molecular Structure; vol. 219; (1990); p. 257 - 262, View in Reaxys 85 of 168

Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

29.9

Partner (Association (MCS))

acetonitrile; phenol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Gonchar, N. P.; Journal of Molecular Structure; vol. 219; (1990); p. 257 - 262, View in Reaxys 86 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

29.9

Partner (Association (MCS))

acetonitrile; phenol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Gonchar, N. P.; Journal of Molecular Structure; vol. 219; (1990); p. 257 - 262, View in Reaxys 87 of 168

Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

29.9

Partner (Association (MCS))

p-cresol

61/412

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Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Gonchar, N. P.; Journal of Molecular Structure; vol. 219; (1990); p. 257 - 262, View in Reaxys 88 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

29.9

Partner (Association (MCS))

p-cresol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Gonchar, N. P.; Journal of Molecular Structure; vol. 219; (1990); p. 257 - 262, View in Reaxys 89 of 168

Description (Association Further physical properties of the complex (MCS)) Partner (Association (MCS))

cetane

Abraham, Michael H.; Whiting, Gary S.; Fuchs, Richard; Chambers, Eric J.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 2; (1990); p. 291 - 300, View in Reaxys 90 of 168

Description (Association NMR spectrum of the complex (MCS)) Partner (Association (MCS))

poly(4-vinylpyridine)

Korb, J.-P.; Sapoval, B.; Chachaty, C.; Tistchenko, A.M.; Journal of Physical Chemistry; vol. 94; nb. 2; (1990); p. 953 - 958, View in Reaxys 91 of 168

Description (Association NMR spectrum of the complex (MCS)) Partner (Association (MCS))

2-Iodophenol

Salman, Salman R.; Kudier, A. R.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 46; nb. 8; (1990); p. 1147 - 1152, View in Reaxys 92 of 168

Description (Association NMR spectrum of the complex (MCS)) Partner (Association (MCS))

2-hydroxybromobenzene

Salman, Salman R.; Kudier, A. R.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 46; nb. 8; (1990); p. 1147 - 1152, View in Reaxys 93 of 168

Description (Association NMR spectrum of the complex (MCS)) Partner (Association (MCS))

2-monochlorophenol

Salman, Salman R.; Kudier, A. R.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 46; nb. 8; (1990); p. 1147 - 1152, View in Reaxys 94 of 168

Description (Association NMR spectrum of the complex (MCS)) Partner (Association (MCS))

2-Fluorophenol

Salman, Salman R.; Kudier, A. R.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 46; nb. 8; (1990); p. 1147 - 1152, View in Reaxys 95 of 168

Description (Association NMR spectrum of the complex (MCS)) Partner (Association (MCS))

SnCl4

62/412

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Kravchenko, E. A.; Morgunov, V. G.; Burtsev, M. Yu.; Buslaev, Yu. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 60; nb. 9.1.; (1990); p. 1945 - 1956,1737 - 1746, View in Reaxys 96 of 168

Description (Association Enthalpy of association (MCS)) Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

hex-1-yne

Koldobskaya, L. L.; Semenov, L. V.; Gaile, A. A.; Rumyantseva, N. V.; J. Appl. Chem. USSR (Engl. Transl.); vol. 62; nb. 3.1; (1989); p. 599 - 603,551 - 555, View in Reaxys 97 of 168

Description (Association Further physical properties of the complex (MCS)) Partner (Association (MCS))

18-crown-6 ether

Elbasyouny, A.; Bruegge, H. J.; Deuten, K. von; Dickel, M.; Knoechel, A.; et al.; Journal of the American Chemical Society; vol. 105; nb. 22; (1983); p. 6568 - 6577, View in Reaxys; Zon, A. van; Jong, F. de; Reinhoudt, D. N.; Torny, G. J.; Onwezen, Y.; Recueil: Journal of the Royal Netherlands Chemical Society; vol. 100; nb. 12; (1981); p. 453 - 459, View in Reaxys; Buchanan, Gerald W.; Morat, Claude; Ratcliffe, Christopher I.; Ripmeester, John A.; Journal of the Chemical Society, Chemical Communications; nb. 18; (1989); p. 1306 - 1308, View in Reaxys 98 of 168

Description (Association Association with compound (MCS)) Partner (Association (MCS))

1,1'-binaphthyl-8,8'-dicarboxylic acid*pyridine (1:1)

Csoeregh, Ingeborg; Czugler, Matyas; Toernroos, Karl W.; Weber, Edwin; Ahrendt, Jochen; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1989); p. 1491 - 1498, View in Reaxys 99 of 168

Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

phenol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Journal of Molecular Structure; vol. 175; (1988); p. 307 - 312, View in Reaxys 100 of 168 Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

4-nitrophenol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Journal of Molecular Structure; vol. 175; (1988); p. 307 - 312, View in Reaxys 101 of 168 Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

3-monochlorophenol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Journal of Molecular Structure; vol. 175; (1988); p. 307 - 312, View in Reaxys 102 of 168 Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

CCl4

63/412

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Partner (Association (MCS))

4-chlorophenol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Journal of Molecular Structure; vol. 175; (1988); p. 307 - 312, View in Reaxys 103 of 168 Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

p-cresol

Titov, E. V.; Shurpach, V. I.; Belkina, G. A.; Journal of Molecular Structure; vol. 175; (1988); p. 307 - 312, View in Reaxys 104 of 168 Description (Association Association with compound (MCS)) Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

water

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

Butane-1,4-diol

Kleeberg, H.; Klein, D.; Luck, W. A. P.; Journal of Physical Chemistry; vol. 91; nb. 12; (1987); p. 3200 - 3203, View in Reaxys 106 of 168 Description (Association IR spectrum of the complex (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

butan-1-ol

Kleeberg, H.; Klein, D.; Luck, W. A. P.; Journal of Physical Chemistry; vol. 91; nb. 12; (1987); p. 3200 - 3203, View in Reaxys 107 of 168 Description (Association IR spectrum of the complex (MCS)) Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

methanol

Kleeberg, H.; Klein, D.; Luck, W. A. P.; Journal of Physical Chemistry; vol. 91; nb. 12; (1987); p. 3200 - 3203, View in Reaxys 108 of 168 Description (Association Enthalpy of association (MCS)) Partner (Association (MCS))

phenylnitrenium ion

64/412

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Meot-Ner (Mautner), Michael; El-Shall, M. Samy; Journal of the American Chemical Society; vol. 108; nb. 15; (1986); p. 4386 - 4390, View in Reaxys 109 of 168 Description (Association Further physical properties of the complex (MCS)) Partner (Association (MCS))

phenylnitrenium ion

Meot-Ner (Mautner), Michael; El-Shall, M. Samy; Journal of the American Chemical Society; vol. 108; nb. 15; (1986); p. 4386 - 4390, View in Reaxys 110 of 168

Description (Association NMR spectrum of the complex (MCS)) Solvent (Association (MCS))

benzene

Temperature (Association (MCS)) [°C]

24.9

Partner (Association (MCS))

18-crown-6 ether

Mosier-Boss, Pamela A.; Popov, Alexander I.; Journal of the American Chemical Society; vol. 107; nb. 22; (1985); p. 6168 - 6174, View in Reaxys 111 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

benzene

Temperature (Association (MCS)) [°C]

24.9

Partner (Association (MCS))

18-crown-6 ether

Mosier-Boss, Pamela A.; Popov, Alexander I.; Journal of the American Chemical Society; vol. 107; nb. 22; (1985); p. 6168 - 6174, View in Reaxys 112 of 168

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

24.9

Partner (Association (MCS))

18-crown-6 ether

Mosier-Boss, Pamela A.; Popov, Alexander I.; Journal of the American Chemical Society; vol. 107; nb. 22; (1985); p. 6168 - 6174, View in Reaxys 113 of 168

Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

CH2Cl2

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

boron trifluoride

Maria, Pierre-Charles; Gal, Jean-Francois; Journal of Physical Chemistry; vol. 89; nb. 7; (1985); p. 1296 - 1304, View in Reaxys 114 of 168

Description (Association Association with compound (MCS)) Partner (Association (MCS))

Nitrobenzene radical anion

Sieck, L. Wayne; Journal of Physical Chemistry; vol. 89; nb. 25; (1985); p. 5552 - 5556, View in Reaxys

65/412

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115 of 168

Description (Association Enthalpy of association (MCS)) Partner (Association (MCS))

methylammonium cation

Meot-Ner (Mautner), Michael; Journal of the American Chemical Society; vol. 106; nb. 5; (1984); p. 1257 - 1264, View in Reaxys 116 of 168

Description (Association IR spectrum of the complex (MCS)) Solvent (Association (MCS))

solid matrix

Temperature (Association (MCS)) [°C]

-259.2

Partner (Association (MCS))

Jacox, Marilyn E.; Journal of Physical Chemistry; vol. 88; nb. 15; (1984); p. 3373 - 3379, View in Reaxys 117 of 168

Description (Association NMR spectrum of the complex (MCS)) Temperature (Association (MCS)) [°C]

-20

Partner (Association (MCS))

4,7,13,16,21-pentaoxa-1,10-diazabicyclo-[8,8,5-tricosane

Schmidt, Emmanuel; Tremillon, Jean-Michel; Kintzinger, Jean-Pierre; Popov, Alexander I.; Journal of the American Chemical Society; vol. 105; nb. 26; (1983); p. 7563 - 7566, View in Reaxys 118 of 168

Description (Association IR spectrum of the complex (MCS)) Temperature (Association (MCS)) [°C]

-259.2

Partner (Association (MCS))

NF3

Jacox, Marilyn E.; Journal of Physical Chemistry; vol. 87; nb. 16; (1983); p. 3126 - 3135, View in Reaxys 119 of 168

Description (Association Association with compound (MCS)) Solvent (Association (MCS))

methylcyclohexane

Temperature (Association (MCS)) [°C]

0 - 90

Partner (Association (MCS))

tris(dimethylamino)phosphine oxide

Fujiwara, Hideaki; Takagi, Tatsuya; Yamazaki, Yutaka; Sasaki, Yoshio; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 78; (1982); p. 347 - 356, View in Reaxys 120 of 168 Description (Association IR spectrum of the complex (MCS)) Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

methanol

Symons, Martyn C. R.; Pay, Nick G. M.; Eaton, Graham; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 78; (1982); p. 1841 - 1846, View in Reaxys 121 of 168 Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

benzene-d6

66/412

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Partner (Association (MCS))

18-crown-6 ether

Boer, Jan A. A. de; Reinhoudt, David N.; Harkema, Sybolt; Hummel, Gerrit J. van; Jong, Feike de; Journal of the American Chemical Society; vol. 104; nb. 15; (1982); p. 4073 - 4076, View in Reaxys 122 of 168 Description (Association Further physical properties of the complex (MCS)) Solvent (Association (MCS))

benzene-d6

Partner (Association (MCS))

18-crown-6 ether

Boer, Jan A. A. de; Reinhoudt, David N.; Harkema, Sybolt; Hummel, Gerrit J. van; Jong, Feike de; Journal of the American Chemical Society; vol. 104; nb. 15; (1982); p. 4073 - 4076, View in Reaxys 123 of 168 Description (Association Further physical properties of the complex (MCS)) Solvent (Association (MCS))

benzene-d6

Partner (Association (MCS))

3,6,9,12,15-pentaoxabicyclolt;15.3.1gt;henicosa-1(21),17,19-triene

Boer, Jan A. A. de; Reinhoudt, David N.; Harkema, Sybolt; Hummel, Gerrit J. van; Jong, Feike de; Journal of the American Chemical Society; vol. 104; nb. 15; (1982); p. 4073 - 4076, View in Reaxys 124 of 168 Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

benzene-d6

Partner (Association (MCS))

3,6,9,12,15-pentaoxabicyclolt;15.3.1gt;henicosa-1(21),17,19-triene

Boer, Jan A. A. de; Reinhoudt, David N.; Harkema, Sybolt; Hummel, Gerrit J. van; Jong, Feike de; Journal of the American Chemical Society; vol. 104; nb. 15; (1982); p. 4073 - 4076, View in Reaxys 125 of 168 Description (Association Dipole moment of the complex (MCS)) Temperature (Association (MCS)) [°C]

19.9

Partner (Association (MCS))

tetrachloromethane

Knoezinger; Kollhoff; Wittenbeck; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 86; nb. 10; (1982); p. 929 - 935, View in Reaxys 126 of 168 Description (Association IR spectrum of the complex (MCS)) Temperature (Association (MCS)) [°C]

4.9

Partner (Association (MCS))

tetrachloromethane

Knoezinger; Kollhoff; Wittenbeck; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 86; nb. 10; (1982); p. 929 - 935, View in Reaxys 127 of 168 Description (Association IR spectrum of the complex (MCS)) Temperature (Association (MCS)) [°C]

40.9

Partner (Association (MCS))

tetrachloromethane; CD3NO2

Knoezinger; Kollhoff; Wittenbeck; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 86; nb. 10; (1982); p. 929 - 935, View in Reaxys

67/412

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128 of 168 Description (Association IR spectrum of the complex (MCS)) Temperature (Association (MCS)) [°C]

40.9

Partner (Association (MCS))

tetrachloromethane; [D3]acetonitrile

Knoezinger; Kollhoff; Wittenbeck; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 86; nb. 10; (1982); p. 929 - 935, View in Reaxys 129 of 168 Description (Association IR spectrum of the complex (MCS)) Temperature (Association (MCS)) [°C]

40.9

Partner (Association (MCS))

tetrachloromethane; [(2)H6]acetone

Knoezinger; Kollhoff; Wittenbeck; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 86; nb. 10; (1982); p. 929 - 935, View in Reaxys 130 of 168 Description (Association IR spectrum of the complex (MCS)) Temperature (Association (MCS)) [°C]

40.9

Partner (Association (MCS))

tetrachloromethane; tetrahydrofuran-d8

Knoezinger; Kollhoff; Wittenbeck; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 86; nb. 10; (1982); p. 929 - 935, View in Reaxys 131 of 168 Description (Association IR spectrum of the complex (MCS)) Temperature (Association (MCS)) [°C]

40.9

Partner (Association (MCS))

tetrachloromethane; dimethylsulfoxide-d6

Knoezinger; Kollhoff; Wittenbeck; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 86; nb. 10; (1982); p. 929 - 935, View in Reaxys 132 of 168 Description (Association IR spectrum of the complex (MCS)) Temperature (Association (MCS)) [°C]

40.9

Partner (Association (MCS))

dimethylsulfoxide-d6

Knoezinger; Kollhoff; Wittenbeck; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 86; nb. 10; (1982); p. 929 - 935, View in Reaxys 133 of 168 Description (Association IR spectrum of the complex (MCS)) Temperature (Association (MCS)) [°C]

40.9

Partner (Association (MCS))

tetrachloromethane; perdeuteriopyridine

Knoezinger; Kollhoff; Wittenbeck; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 86; nb. 10; (1982); p. 929 - 935, View in Reaxys 134 of 168 Description (Association IR spectrum of the complex (MCS)) Solvent (Association (MCS))

CCl4

68/412

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Partner (Association (MCS))

HClO4

Karelin; Journal of applied spectroscopy; vol. 37; nb. 3; (1982); p. 1052 - 1058, View in Reaxys 135 of 168 Description (Association IR spectrum of the complex (MCS)) Partner (Association (MCS))

Pentachlorophenol

Karelin; Journal of applied spectroscopy; vol. 37; nb. 3; (1982); p. 1052 - 1058, View in Reaxys 136 of 168 Description (Association IR spectrum of the complex (MCS)) Partner (Association (MCS))

Mg(ClO4)2

Perelygin, L. S.; Klimchuk, M. A.; Journal of Applied Spectroscopy; vol. 36; (1982); p. 531 - 535; Zhurnal Prikladnoi Spektroskopii; vol. 36; nb. 5; (1982); p. 761 - 766, View in Reaxys 137 of 168 Description (Association IR spectrum of the complex (MCS)) Partner (Association (MCS))

LiClO4

Perelygin, L. S.; Klimchuk, M. A.; Journal of Applied Spectroscopy; vol. 36; (1982); p. 531 - 535; Zhurnal Prikladnoi Spektroskopii; vol. 36; nb. 5; (1982); p. 761 - 766, View in Reaxys 138 of 168 Description (Association IR spectrum of the complex (MCS)) Partner (Association (MCS))

LiNCS

Perelygin, L. S.; Klimchuk, M. A.; Journal of Applied Spectroscopy; vol. 36; (1982); p. 531 - 535; Zhurnal Prikladnoi Spektroskopii; vol. 36; nb. 5; (1982); p. 761 - 766, View in Reaxys 139 of 168 Description (Association Association with compound (MCS)) Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

tert -butyl hydrogen peroxide

Makitra; Zhukovskii; Pirig; Chernyak; Journal of applied spectroscopy; vol. 36; nb. 6; (1982); p. 680 - 685, View in Reaxys 140 of 168 Description (Association IR spectrum of the complex (MCS)) Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

tert -butyl hydrogen peroxide

Makitra; Zhukovskii; Pirig; Chernyak; Journal of applied spectroscopy; vol. 36; nb. 6; (1982); p. 680 - 685, View in Reaxys 141 of 168 Description (Association NMR spectrum of the complex (MCS)) Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

methanol

Symons, Martyn C.R.; Thomas, Vicky K.; Fletcher, Nigel J.; Pay, Nicholas G.; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 77; (1981); p. 1899 - 1912, View in Reaxys 142 of 168 Description (Association Enthalpy of association (MCS))

69/412

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Temperature (Association (MCS)) [°C]

24.9

Partner (Association (MCS))

chloroform

Tsvetkov, V. G.; Kupriyanov, V. F.; Vesnovskii, B. P.; Aleksandrov, Yu. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 51; nb. 7; (1981); p. 1456 - 1459,1235 - 1238, View in Reaxys 143 of 168 Description (Association Enthalpy of association (MCS)) Temperature (Association (MCS)) [°C]

24.9

Partner (Association (MCS))

Gallium trichloride

Tsvetkov, V. G.; Kupriyanov, V. F.; Vesnovskii, B. P.; Aleksandrov, Yu. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 51; nb. 7; (1981); p. 1456 - 1459,1235 - 1238, View in Reaxys 144 of 168 Description (Association Enthalpy of association (MCS)) Temperature (Association (MCS)) [°C]

24.9

Partner (Association (MCS))

boron tribromide

Tsvetkov, V. G.; Kupriyanov, V. F.; Vesnovskii, B. P.; Aleksandrov, Yu. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 51; nb. 7; (1981); p. 1456 - 1459,1235 - 1238, View in Reaxys 145 of 168 Description (Association NMR spectrum of the complex (MCS)) Partner (Association (MCS))

18-crown-6 ether

Zon, A. van; Jong, F. de; Reinhoudt, D. N.; Torny, G. J.; Onwezen, Y.; Recueil: Journal of the Royal Netherlands Chemical Society; vol. 100; nb. 12; (1981); p. 453 - 459, View in Reaxys 146 of 168 Description (Association NMR spectrum of the complex (MCS)) Solvent (Association (MCS))

neat (no solvent)

Partner (Association (MCS))

tris(acetylacetonato)chromium(III)

Witanowski, M.; Stefaniak, L.; Kamienski, B.; Biernat, S.; Webb, G. A.; Journal of Magnetic Resonance (1969-1992); vol. 43; nb. 3; (1981); p. 456 - 462, View in Reaxys 147 of 168 Description (Association Association with compound (MCS)) Partner (Association (MCS))

hexakis-(3,4-methylenedioxybenzylthiomethyl)benzene

Hardy, Andrew D. U.; MacNicol, David D.; Swanson, Stephen; Wilson, Derek R.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1980); p. 999 - 1005, View in Reaxys 148 of 168 Description (Association Association with compound (MCS)) Partner (Association (MCS))

hexakis-(2-chlorobenzylthiomethyl)benzene

Hardy, Andrew D. U.; MacNicol, David D.; Swanson, Stephen; Wilson, Derek R.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1980); p. 999 - 1005, View in Reaxys 149 of 168 Description (Association Dipole moment of the complex (MCS)) Solvent (Association (MCS))

benzene

70/412

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Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

AlBr3

Gur'yanova, E. N.; Isaeva, E. S.; Shifrina, R. R.; Lechkina, L. I.; Kharlamova, E. N.; Terent'ev, V. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 50; nb. 3; (1980); p. 667 - 673,547 - 552, View in Reaxys 150 of 168 Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

benzene

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

AlBr3

Gur'yanova, E. N.; Isaeva, E. S.; Shifrina, R. R.; Lechkina, L. I.; Kharlamova, E. N.; Terent'ev, V. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 50; nb. 3; (1980); p. 667 - 673,547 - 552, View in Reaxys 151 of 168 Description (Association IR spectrum of the complex (MCS)) Solvent (Association (MCS))

benzene

Partner (Association (MCS))

AlBr3

Gur'yanova, E. N.; Isaeva, E. S.; Shifrina, R. R.; Lechkina, L. I.; Kharlamova, E. N.; Terent'ev, V. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 50; nb. 3; (1980); p. 667 - 673,547 - 552, View in Reaxys 152 of 168 Description (Association IR spectrum of the complex (MCS)) Partner (Association (MCS))

TBA thiocyanate

Bacelon, P.; Corset, J.; Loze, C. de; Journal of Solution Chemistry; vol. 9; (1980); p. 129 - 140, View in Reaxys 153 of 168 Description (Association IR spectrum of the complex (MCS)) Partner (Association (MCS))

LiSCN

Bacelon, P.; Corset, J.; Loze, C. de; Journal of Solution Chemistry; vol. 9; (1980); p. 129 - 140, View in Reaxys 154 of 168 Description (Association Further physical properties of the complex (MCS)) Partner (Association (MCS))

LiSCN

Bacelon, P.; Corset, J.; Loze, C. de; Journal of Solution Chemistry; vol. 9; (1980); p. 129 - 140, View in Reaxys 155 of 168 Description (Association IR spectrum of the complex (MCS)) Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

butan-1-ol

Iogansen, A. V.; Rassadin, B. V.; Sorokina, N. P.; Journal of Applied Spectroscopy; vol. 32; nb. 6; (1980); p. 646 651; Zhurnal Prikladnoi Spektroskopii; vol. 32; nb. 6; (1980); p. 1089 - 1095, View in Reaxys 156 of 168 Description (Association Association with compound (MCS)) Temperature (Association (MCS)) [°C]

71/412

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Partner (Association (MCS))

butan-1-ol

Iogansen, A. V.; Rassadin, B. V.; Sorokina, N. P.; Journal of Applied Spectroscopy; vol. 32; nb. 6; (1980); p. 646 651; Zhurnal Prikladnoi Spektroskopii; vol. 32; nb. 6; (1980); p. 1089 - 1095, View in Reaxys 157 of 168 Description (Association Further physical properties of the complex (MCS)) Solvent (Association (MCS))

H2O

Partner (Association (MCS))

anthracene; sodium lauryl sulfate

Ponomareva; Zaev; Journal of applied spectroscopy; vol. 33; nb. 3; (1980); p. 940 - 944, View in Reaxys 158 of 168 Description (Association IR spectrum of the complex (MCS)) Partner (Association (MCS))

acetic acid

acetic acid; LiClO4

Perelygin, I. S.; Afanas'eva, A. M.; Journal of Applied Spectroscopy; vol. 33; nb. 4; (1980); p. 1100 - 1106; Zhurnal Prikladnoi Spektroskopii; vol. 33; nb. 4; (1980); p. 680 - 687, View in Reaxys 160 of 168 Description (Association Spectrum of the complex (MCS)) Singh et al.; Transactions of the Faraday Society; vol. 62; (1966); p. 1056,1058, View in Reaxys; Detoni et al.; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1970); p. 2851,2852, View in Reaxys; Belogorodskaya; Nikolayev; ; vol. 18; nb. 8; (1977); p. 2104 - 2110, View in Reaxys; Yoshida; Takabayashi; Nippon Kagaku Zasshi; vol. 87; (1966); p. 452,453,454, View in Reaxys; Regis; Corset; Canadian Journal of Chemistry; vol. 51; (1973); p. 3577,3582, 3584, 3585, View in Reaxys 161 of 168 Description (Association Association with compound (MCS)) Mohr et al.; Journal of the American Chemical Society; vol. 87; (1965); p. 3048,3049, View in Reaxys; McTigue; Renowden; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 71; (1975); p. 1784,1786, View in Reaxys; Johnston et al.; Journal of the American Chemical Society; vol. 91; (1969); p. 5715,5716, View in Reaxys; Regis; Corset; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 69; (1972); p. 1508, View in Reaxys; Iogansen et al.; Journal of Applied Spectroscopy; vol. 18; (1973); p. 499; ; p. 676, View in Reaxys 162 of 168 Description (Association Enthalpy of association (MCS)) Rosenberg et al.; Spectroscopy Letters; vol. 5; (1972); p. 75,77, View in Reaxys 163 of 168 Description (Association Stability constant of the complex with ... (MCS)) Krueger; Mettee; Canadian Journal of Chemistry; vol. 42; (1964); p. 288,289, View in Reaxys 164 of 168 Description (Association Association with compound (MCS)) Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

2,4-dimethyl-3-pentanol

De Maine et al.; Spectrochimica Acta; vol. 15; (1959); p. 1054, View in Reaxys 165 of 168 Description (Association Association with compound (MCS))

72/412

2016-04-19 03:35:30

Solvent (Association (MCS))

toluene

Partner (Association (MCS))

benzonitrile

Tronow; Strel'nikowa; Izv.Tomsk.politech.Inst.; vol. 83; (1956); p. 98; Chem.Abstr.; (1959); p. 12804, View in Reaxys 166 of 168 Description (Association Association with compound (MCS)) Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

phenol

Sato; Nagakura; Nippon Kagaku Zasshi; vol. 76; (1955); p. 1007; Chem.Abstr.; (1956); p. 5406, View in Reaxys 167 of 168 Description (Association Association with compound (MCS)) Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

3-monochlorophenol

Sato; Nagakura; Nippon Kagaku Zasshi; vol. 76; (1955); p. 1007; Chem.Abstr.; (1956); p. 5406, View in Reaxys 168 of 168 Description (Association Association with compound (MCS)) Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

4-chlorophenol

Sato; Nagakura; Nippon Kagaku Zasshi; vol. 76; (1955); p. 1007; Chem.Abstr.; (1956); p. 5406, View in Reaxys Azeotropes (MCS) (96) 1 of 96

Malesinska; Malesinski; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 11; (1963); p. 475,476, View in Reaxys; Malesinska; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 12; (1964); p. 853, View in Reaxys; Marinichev; Vertsman; J. Appl. Chem. USSR (Engl. Transl.); vol. 46; (1973); p. 355,368, View in Reaxys

2 of 96

Azeotropes

isopropyl alcohol; water

Kogan; Tolstowa; Zhurnal Fizicheskoi Khimii; vol. 33; (1959); p. 276; Chem.Abstr.; (1959); p. 20995, View in Reaxys 3 of 96

Temperature (Azeotropes (MCS)) [°C]

Azeotropes

benzene

Brown; Smith; Australian Journal of Chemistry; vol. 8; (1955); p. 501,503, View in Reaxys 4 of 96

Temperature (Azeotropes (MCS)) [°C]

Azeotropes

tetrachloromethane

Brown; Smith; Australian Journal of Chemistry; vol. 8; (1955); p. 501,503, View in Reaxys 5 of 96

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

methanol

Desseigne; Belliot; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 49; (1952); p. 46, View in Reaxys 6 of 96

Temperature (Azeotropes (MCS)) [°C]

53.8

73/412

2016-04-19 03:35:30

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

silicon tetrachloride

Sauer; Hadsell; Journal of the American Chemical Society; vol. 70; (1948); p. 4258, View in Reaxys 7 of 96

Temperature (Azeotropes (MCS)) [°C]

Azeotropes

water; isopropyl alcohol

Schumacher; Hunt; Industrial and Engineering Chemistry; vol. 34; (1942); p. 703, View in Reaxys 8 of 96

Temperature (Azeotropes (MCS)) [°C]

82.3

Azeotropes

water; propyl alcohol

Fowler; Hunt; Industrial and Engineering Chemistry; vol. 33; (1941); p. 91, View in Reaxys 9 of 96

Temperature (Azeotropes (MCS)) [°C]

101.1

Azeotropes

acetic acid

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 20, View in Reaxys 10 of 96

Temperature (Azeotropes (MCS)) [°C]

64.6

Azeotropes

methanol

Lecat,M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 47; (1928); p. 15,16; Ann. Soc. scient. Bruxelles; vol. 47 I; (1927); p. 154, View in Reaxys 11 of 96

Temperature (Azeotropes (MCS)) [°C]

97.3

Azeotropes

butyl alcohol

Lecat,M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 47; (1928); p. 15,16; Ann. Soc. scient. Bruxelles; vol. 47 I; (1927); p. 154, View in Reaxys 12 of 96

Temperature (Azeotropes (MCS)) [°C]

70.6

Azeotropes

propyl bromide

Lecat; Ann.Soc.scient.Bruxelles; vol. 48 I; (1928); p. 16,116,117, View in Reaxys 13 of 96

Temperature (Azeotropes (MCS)) [°C]

Azeotropes

ethanol

Lecat,M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 47; (1928); p. 15,16; Ann. Soc. scient. Bruxelles; vol. 47 I; (1927); p. 154, View in Reaxys 14 of 96

Temperature (Azeotropes (MCS)) [°C]

68.4

Azeotropes

isobutyl chloride

Lecat,M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 47; (1928); p. 15,16; Ann. Soc. scient. Bruxelles; vol. 47 I; (1927); p. 154, View in Reaxys 15 of 96

Temperature (Azeotropes (MCS)) [°C]

Azeotropes

tetrachloroethylene

Lecat; Ann.Soc.scient.Bruxelles; vol. 48 I; (1928); p. 16,116,117, View in Reaxys 16 of 96

Temperature (Azeotropes (MCS)) [°C]

Azeotropes

dimethylethylcarbinol

Lecat,M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 47; (1928); p. 15,16; Ann. Soc. scient. Bruxelles; vol. 47 I; (1927); p. 154, View in Reaxys

74/412

2016-04-19 03:35:30

17 of 96

Temperature (Azeotropes (MCS)) [°C]

79.2

Azeotropes

benzene

Lecat; Ann.Soc.scient.Bruxelles; vol. 47I; (1927); p. 152,153, View in Reaxys 18 of 96

Temperature (Azeotropes (MCS)) [°C]

98.5

Azeotropes

butyl formate

Lecat; Ann.Soc.scient.Bruxelles; vol. 47I; (1927); p. 152,153, View in Reaxys 19 of 96

Temperature (Azeotropes (MCS)) [°C]

95.5

Azeotropes

ethyl propionate

Lecat; Recueil des Travaux Chimiques des Pays-Bas; vol. 46; (1927); p. 243; Ann.Soc.scient.Bruxelles; vol. 47 I; (1927); p. 112,151,155, View in Reaxys 20 of 96

Temperature (Azeotropes (MCS)) [°C]

94.1

Azeotropes

isobutyl alcohol

Lecat; Ann.Soc.scient.Bruxelles; vol. 47I; (1927); p. 152,153, View in Reaxys 21 of 96

Temperature (Azeotropes (MCS)) [°C]

100.3

Azeotropes

isobutylcarbinol

Lecat; Ann.Soc.scient.Bruxelles; vol. 47I; (1927); p. 152,153, View in Reaxys 22 of 96

Temperature (Azeotropes (MCS)) [°C]

79.1

Azeotropes

isopropyl alcohol

Lecat; Ann.Soc.scient.Bruxelles; vol. 47I; (1927); p. 152,153, View in Reaxys 23 of 96

Temperature (Azeotropes (MCS)) [°C]

97.4

Azeotropes

methyl butyrate

Lecat; Ann.Soc.scient.Bruxelles; vol. 47I; (1927); p. 152,153, View in Reaxys; Lecat; Recueil des Travaux Chimiques des Pays-Bas; vol. 46; (1927); p. 243; Ann.Soc.scient.Bruxelles; vol. 47 I; (1927); p. 112,151,155, View in Reaxys 24 of 96

Temperature (Azeotropes (MCS)) [°C]

Azeotropes

chloral

Lecat; Recueil des Travaux Chimiques des Pays-Bas; vol. 45; (1926); p. 624; Ann.Soc.scient.Bruxelles; vol. 47 I; (1927); p. 24, View in Reaxys 25 of 96

Temperature (Azeotropes (MCS)) [°C]

97.6

Azeotropes

propyl acetate

Lecat; Recueil des Travaux Chimiques des Pays-Bas; vol. 45; (1926); p. 624; Ann.Soc.scient.Bruxelles; vol. 47 I; (1927); p. 24, View in Reaxys 26 of 96

Temperature (Azeotropes (MCS)) [°C]

93.8

Azeotropes

isobutyl formate

Lecat; Recueil des Travaux Chimiques des Pays-Bas; vol. 45; (1926); p. 624; Ann.Soc.scient.Bruxelles; vol. 47 I; (1927); p. 24, View in Reaxys 27 of 96

Temperature (Azeotropes (MCS)) [°C]

81.3

Azeotropes

methylcyclohexane

75/412

2016-04-19 03:35:30

Lecat; Ann.Soc.scient.Bruxelles; vol. 45; (1926); p. 175, View in Reaxys 28 of 96

Temperature (Azeotropes (MCS)) [°C]

87.3

Azeotropes

dichlorobromomethane

Lecat; Recueil des Travaux Chimiques des Pays-Bas; vol. 45; (1926); p. 624; Ann.Soc.scient.Bruxelles; vol. 47 I; (1927); p. 24, View in Reaxys 29 of 96

Temperature (Azeotropes (MCS)) [°C]

71.3

Azeotropes

carbon tetrachloride

Lecat; Recueil des Travaux Chimiques des Pays-Bas; vol. 45; (1926); p. 624; Ann.Soc.scient.Bruxelles; vol. 47 I; (1927); p. 24, View in Reaxys 30 of 96

Temperature (Azeotropes (MCS)) [°C]

94.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

methylisopropyl ketone

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.201, View in Reaxys 31 of 96

Temperature (Azeotropes (MCS)) [°C]

98.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

methylpropylcarbinol

Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.102, View in Reaxys; Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys 32 of 96

Temperature (Azeotropes (MCS)) [°C]

93.1

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

dimethylethyl-carbinol

Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.102, View in Reaxys; Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys 33 of 96

Temperature (Azeotropes (MCS)) [°C]

96.4

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

methylisopropylcarbinol

Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.102, View in Reaxys; Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys 34 of 96

Temperature (Azeotropes (MCS)) [°C]

90.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

1.3-dimethyl-cyclohexane

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.311, View in Reaxys 35 of 96

Temperature (Azeotropes (MCS)) [°C]

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

hexane

76/412

2016-04-19 03:35:30

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.311, View in Reaxys 36 of 96

Temperature (Azeotropes (MCS)) [°C]

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

octane

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.311, View in Reaxys 37 of 96

Temperature (Azeotropes (MCS)) [°C]

100.6

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

dioxane

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.328, View in Reaxys 38 of 96

Temperature (Azeotropes (MCS)) [°C]

79.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

benzene

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.311, View in Reaxys 39 of 96

Temperature (Azeotropes (MCS)) [°C]

80.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

heptane

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.311, View in Reaxys 40 of 96

Temperature (Azeotropes (MCS)) [°C]

96.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

toluene

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.311, View in Reaxys 41 of 96

Temperature (Azeotropes (MCS)) [°C]

83.6

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

water

Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.355, View in Reaxys; Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys 42 of 96

Temperature (Azeotropes (MCS)) [°C]

100.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

pyridine

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.330, View in Reaxys

77/412

2016-04-19 03:35:30

43 of 96

Temperature (Azeotropes (MCS)) [°C]

92.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

chloral

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.161, View in Reaxys 44 of 96

Temperature (Azeotropes (MCS)) [°C]

57.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

diallyl

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.311, View in Reaxys 45 of 96

Temperature (Azeotropes (MCS)) [°C]

64.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

methanol

Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.102, View in Reaxys; Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys 46 of 96

Temperature (Azeotropes (MCS)) [°C]

100.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

pinacolin

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.201, View in Reaxys 47 of 96

Temperature (Azeotropes (MCS)) [°C]

70.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

cyclohexane

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.311, View in Reaxys 48 of 96

Temperature (Azeotropes (MCS)) [°C]

74.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

cyclohexene

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.311, View in Reaxys 49 of 96

Temperature (Azeotropes (MCS)) [°C]

85.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

diisobutyl

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.311, View in Reaxys 50 of 96

Temperature (Azeotropes (MCS)) [°C]

78/412

2016-04-19 03:35:30

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

allyl iodide

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.291, View in Reaxys 51 of 96

Temperature (Azeotropes (MCS)) [°C]

99.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

butyl iodide

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.291, View in Reaxys 52 of 96

Temperature (Azeotropes (MCS)) [°C]

100.4

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

chloropicrin

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.328, View in Reaxys 53 of 96

Temperature (Azeotropes (MCS)) [°C]

101.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

acetic acid

Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.23, View in Reaxys; Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys 54 of 96

Temperature (Azeotropes (MCS)) [°C]

47.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

cyclopentane

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.311, View in Reaxys 55 of 96

Temperature (Azeotropes (MCS)) [°C]

54.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

diisopropyl

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.311, View in Reaxys 56 of 96

Temperature (Azeotropes (MCS)) [°C]

71.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

ethyl iodide

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.291, View in Reaxys 57 of 96

Temperature (Azeotropes (MCS)) [°C]

69.8

Pressure (Azeotropes (MCS)) [Torr]

760

79/412

2016-04-19 03:35:30

Azeotropes

allyl bromide

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.291, View in Reaxys 58 of 96

Temperature (Azeotropes (MCS)) [°C]

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

butyl bromide

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.291, View in Reaxys 59 of 96

Temperature (Azeotropes (MCS)) [°C]

89.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

propyl iodide

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.291, View in Reaxys 60 of 96

Temperature (Azeotropes (MCS)) [°C]

37.7

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

ethyl nitrate

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.256, View in Reaxys 61 of 96

Temperature (Azeotropes (MCS)) [°C]

98.7

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

butyl formate

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.256, View in Reaxys 62 of 96

Temperature (Azeotropes (MCS)) [°C]

100.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

propyl nitrate

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.256, View in Reaxys 63 of 96

Temperature (Azeotropes (MCS)) [°C]

89.3

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

allyl alcohol

Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.102, View in Reaxys; Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys 64 of 96

Temperature (Azeotropes (MCS)) [°C]

97.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

butyl alcohol

80/412

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Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.102, View in Reaxys; Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys 65 of 96

Temperature (Azeotropes (MCS)) [°C]

75.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

butyl chloride

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.291, View in Reaxys 66 of 96

Temperature (Azeotropes (MCS)) [°C]

94.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isopentyl nitrite

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.256, View in Reaxys 67 of 96

Temperature (Azeotropes (MCS)) [°C]

97.9

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

methyl butyrate

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.256, View in Reaxys 68 of 96

Temperature (Azeotropes (MCS)) [°C]

97.1

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

formic acid

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>, View in Reaxys 69 of 96

Temperature (Azeotropes (MCS)) [°C]

99.1

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

diethyl ketone

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.201, View in Reaxys 70 of 96

Temperature (Azeotropes (MCS)) [°C]

89.3

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

propyl alcohol

Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.102, View in Reaxys; Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys 71 of 96

Temperature (Azeotropes (MCS)) [°C]

97.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isopentyl bromide

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.291, View in Reaxys

81/412

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72 of 96

Temperature (Azeotropes (MCS)) [°C]

96.7

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isobutyl iodide

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.291, View in Reaxys 73 of 96

Temperature (Azeotropes (MCS)) [°C]

93.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

butyl mercaptan

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.329, View in Reaxys 74 of 96

Temperature (Azeotropes (MCS)) [°C]

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

diethyl sulfide

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.329, View in Reaxys 75 of 96

Temperature (Azeotropes (MCS)) [°C]

100.6

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isoamyl alcohol

Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.102, View in Reaxys; Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys 76 of 96

Temperature (Azeotropes (MCS)) [°C]

88.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isopentyl chloride

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.291, View in Reaxys 77 of 96

Temperature (Azeotropes (MCS)) [°C]

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isobutyl bromide

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.291, View in Reaxys 78 of 96

Temperature (Azeotropes (MCS)) [°C]

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isopropyl iodide

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.291, View in Reaxys 79 of 96

Temperature (Azeotropes (MCS)) [°C]

82/412

2016-04-19 03:35:30

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

ethyl propionate

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.256, View in Reaxys 80 of 96

Temperature (Azeotropes (MCS)) [°C]

94.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isobutyl formate

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.256, View in Reaxys 81 of 96

Temperature (Azeotropes (MCS)) [°C]

89.3

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isopropyl acetate

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.256, View in Reaxys 82 of 96

Temperature (Azeotropes (MCS)) [°C]

94.6

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isobutyl alcohol

Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.102, View in Reaxys; Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys 83 of 96

Temperature (Azeotropes (MCS)) [°C]

68.4

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isobutyl chloride

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.291, View in Reaxys 84 of 96

Temperature (Azeotropes (MCS)) [°C]

100

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

ethyl isobutyrate

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.256, View in Reaxys 85 of 96

Temperature (Azeotropes (MCS)) [°C]

91.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

methyl isobutyrate

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.256, View in Reaxys 86 of 96

Temperature (Azeotropes (MCS)) [°C]

97.4

Pressure (Azeotropes (MCS)) [Torr]

760

83/412

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Azeotropes

diethylcarbinol

Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.102, View in Reaxys; Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys 87 of 96

Temperature (Azeotropes (MCS)) [°C]

79.4

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isopropyl alcohol

Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.102, View in Reaxys; Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys 88 of 96

Temperature (Azeotropes (MCS)) [°C]

81.4

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

trichloroethylene

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.291, View in Reaxys 89 of 96

Temperature (Azeotropes (MCS)) [°C]

99.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

diisopropyl sulfide

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.329, View in Reaxys 90 of 96

Temperature (Azeotropes (MCS)) [°C]

99.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

methylpropyl ketone

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.201, View in Reaxys 91 of 96

Temperature (Azeotropes (MCS)) [°C]

91.1

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

#sec!-butyl alcohol

Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.102, View in Reaxys; Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys 92 of 96

Temperature (Azeotropes (MCS)) [°C]

64.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

methylcyclopentane

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.311, View in Reaxys 93 of 96

Temperature (Azeotropes (MCS)) [°C]

72.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

#tert!-butyl bromide

84/412

2016-04-19 03:35:30

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.291, View in Reaxys 94 of 96

Temperature (Azeotropes (MCS)) [°C]

79.4

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

#tert!-butyl alcohol

Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.102, View in Reaxys; Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys 95 of 96

Temperature (Azeotropes (MCS)) [°C]

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

tetrachloroethylene

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.291, View in Reaxys 96 of 96

Temperature (Azeotropes (MCS)) [°C]

44.3

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

carbon disulfide

Horsley,L.H.; Azeotropic Data, Advances in Chemistry Series Nr.6 <Washington 1952>S.269, View in Reaxys; Lecat,M.; Tables azeotropiques,2.Aufl.<Bruessel 1949>S.329, View in Reaxys Boundary Surface Phenomena (MCS) (19) 1 of 19

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

hexanoic acid

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

valeric acid

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

butyric acid

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

acetic acid

85/412

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Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Temperature (Boundary Surface Phenomena (MCS)) [°C]

22.5

Partner (Boundary Surface Phenomena (MCS))

2,6,10,15,19,23-hexamethyltetracosane

Riddle Jr.; Fowkes; Journal of the American Chemical Society; vol. 112; nb. 9; (1990); p. 3259 - 3264, View in Reaxys 6 of 19

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

1,4-dioxane

Kudrya, T. P.; Tel'biz, G. M.; Russian Journal of Physical Chemistry; vol. 57; nb. 9; (1983); p. 1414 - 1415; Zhurnal Fizicheskoi Khimii; vol. 57; (1983); p. 2328 - 2329, View in Reaxys 7 of 19

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

1,4-dioxane; butan-1-ol

Kudrya, T. P.; Tel'biz, G. M.; Russian Journal of Physical Chemistry; vol. 57; nb. 9; (1983); p. 1414 - 1415; Zhurnal Fizicheskoi Khimii; vol. 57; (1983); p. 2328 - 2329, View in Reaxys 8 of 19

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

water

Murphy et al.; Industrial and Engineering Chemistry; vol. 49; (1975); p. 1035,1036,1037, View in Reaxys 9 of 19

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

im System mit Wasser.

Murphy et al.; Industrial and Engineering Chemistry; vol. 49; (1975); p. 1035,1036,1037, View in Reaxys 10 of 19

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

water; acetic acid

Murphy et al.; Industrial and Engineering Chemistry; vol. 49; (1975); p. 1035,1036,1037, View in Reaxys 11 of 19

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

im ternaeren System mit Wasser und Essigsaeure.

86/412

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Murphy et al.; Industrial and Engineering Chemistry; vol. 49; (1975); p. 1035,1036,1037, View in Reaxys 12 of 19

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Schroeder; Kintner; AIChE Journal; vol. 11; (1975); p. 5, View in Reaxys 13 of 19

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

zwischen Nitromethan und Heptan.

Sinfelt; Drickamer; Journal of Chemical Physics; vol. 23; (1955); p. 1095,1097, View in Reaxys 14 of 19

Description (Boundary Surface Phenomena (MCS))

Surface tension

Comment (Boundary Surface Phenomena (MCS))

mit unverzweigten Alkansaeuren.

Jones; Saunders; Journal of the Chemical Society; (1951); p. 2944,2946,2947, View in Reaxys 15 of 19

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

benzene

Michaels et al.; Industrial and Engineering Chemistry; vol. 42; (1950); p. 2332,2334, View in Reaxys 16 of 19

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

propan-1-ol

Michaels et al.; Industrial and Engineering Chemistry; vol. 42; (1950); p. 2332,2334, View in Reaxys 17 of 19

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

propan-1-ol; benzene

Michaels et al.; Industrial and Engineering Chemistry; vol. 42; (1950); p. 2332,2334, View in Reaxys 18 of 19

Description (Boundary Surface Phenomena (MCS))

Surface tension

Temperature (Boundary Surface Phenomena (MCS)) [°C]

Partner (Boundary Surface Phenomena (MCS))

benzene

Hammick; Andrew; Journal of the Chemical Society; (1929); p. 756, View in Reaxys 19 of 19

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

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Comment (Boundary Surface Phenomena (MCS))

zwischen Nitromethan und Wasser bei 20grad.

Harkins; Clark; Roberts; Journal of the American Chemical Society; vol. 42; (1920); p. 703, View in Reaxys Circular Dichroism (1) References Hayward; Totty; Canadian Journal of Chemistry; vol. 49; (1971); p. 624, View in Reaxys; Barth et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1979); p. 907,908, View in Reaxys Compressibility (4) Description (Com- Comment (Compressibility) pressibility) Isothermal compressibility

References Uosaki, Yasuhiro; Mutsumura, Hajime; Wakasa, Shinji; Moriyoshi, Takahashi; Journal of Chemical Thermodynamics; vol. 22; nb. 3; (1990); p. 313 - 318, View in Reaxys; Brodskii, I. A.; Libov, V. S.; Perova, T. S.; Shcherbinin, M. B.; Russian Journal of Physical Chemistry; vol. 54; nb. 5; (1980); p. 678 - 681; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 5; (1980); p. 1187 - 1190, View in Reaxys

Adiabatic compressibility

aus der Schallgeschwindigkeit bei 28grad.

Bhimasenachar; Venkateswarlu; Proceedings - Indian Academy of Sciences, Section A; vol. 11; p. 29; Chem.Abstr.; (1940); p. 3553, View in Reaxys

Adiabatic compressibility

bei 25grad und 30grad.

Shiba; Scientific Papers of the Institute of Physical and Chemical Research (Japan); vol. 16; p. 211,219,221; Chem. Zentralbl.; vol. 102; nb. II; (1931); p. 3587, View in Reaxys

Isothermal compressibility

zwischen 0 und 8 Atm.

Hebeisen; Annalen der Physik (Weinheim, Germany); vol. <4> 77; (1925); p. 217, View in Reaxys

Conformation (4) Object of Investi- Comment (Congation formation)

References

Conformer equilibrium

Chauvel, J. Paul; True, Nancy S.; Journal of Physical Chemistry; vol. 87; nb. 9; (1983); p. 1622 - 1625, View in Reaxys; Cataliotti, R. S.; Distefano, M. R.; Mariani, L.; Morresi, A.; Paliani, G.; et al.; Berichte der Bunsen-Gesellschaft; vol. 98; nb. 12; (1994); p. 1613 - 1618, View in Reaxys

Energy difference between the conformers

Chauvel, J. Paul; True, Nancy S.; Journal of Physical Chemistry; vol. 87; nb. 9; (1983); p. 1622 - 1625, View in Reaxys; Ruoff, Rodney S.; Kulp, Thomas J.; McDonald, J. D.; Journal of Chemical Physics; vol. 81; nb. 10; (1984); p. 4414 - 4420, View in Reaxys

Conformation

Scott; Scheraga; Journal of Chemical Physics; vol. 42; (1965); p. 2209,2214, View in Reaxys; Mezey et al.; Canadian Journal of Chemistry; vol. 54; (1976); p. 2526, View in Reaxys; Dachis et al.; Voprosy Stereokhimii; vol. 3; (1973); p. 91; Chem.Abstr.; vol. 81; nb. 151330; (1974), View in Reaxys; Engelbrecht et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 28; (1973); p. 709, View in Reaxys

Conformation

Die freie Drehbar- Pitzer; Gwinn; Journal of the American Chemical Society; vol. 63; (1941); p. 3313, keit um die C-NView in Reaxys; de Vries; Collins; Journal of the American Chemical Society; vol. 64; Bindung ist ge(1942); p. 1225, View in Reaxys hemmt durch ein Potentialschwelle von ca. 800 cal/ Mol.

Critical Density (1) Critical Density References [g·cm-3] 0.352

Griffin; Journal of the American Chemical Society; vol. 71; (1949); p. 1423, View in Reaxys

Critical Pressure (2) Critical Pressure References [Torr] 47351.3

Srivastava, Rakesh; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 30; nb. 3; (1985); p. 313 - 318, View in Reaxys

47424

Griffin; Journal of the American Chemical Society; vol. 71; (1949); p. 1423, View in Reaxys

Critical Temperature (3) Critical Tempera- References ture [°C]

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314.85

Srivastava, Rakesh; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 30; nb. 3; (1985); p. 313 - 318, View in Reaxys Tsvetkov; Rabinovich; Russian Journal of Physical Chemistry; vol. 47; (1973); p. 1355; ; p. 2403, View in Reaxys; Pavlova et al.; Russian Journal of Physical Chemistry; vol. 49; (1975); p. 1693; ; p. 2874, View in Reaxys

315

Griffin; Journal of the American Chemical Society; vol. 71; (1949); p. 1423, View in Reaxys

Cross-Sections (1) Description References (Cross-Sections) Collision crosssection

Asher; Haas; Journal of Chemical Physics; vol. 71; (1979); p. 2724, View in Reaxys; Christophorou; Christodoulides; Journal of Physics B: Atomic and Molecular Physics; vol. 2; (1969); p. 71,80, View in Reaxys

Crystal Phase (6) Description (Crys- Comment (Crystal References tal Phase) Phase) Crystal structure determination

a=5.18 Angstroem, b=6.24 Angstroem, c=8.52 Angstroem.; Temperature: 4.2 K. Method of determination: X-ray Diffraction

Crystal structure determination

a=5.2 Angstroem, Cromer, Don T.; Ryan, Robert R.; Schiferl, David; Journal of Physical Chemistry; vol. b=6.25 Ang89; nb. 11; (1985); p. 2315 - 2318, View in Reaxys stroem, c=8.56 Angstroem.; Temperature: 78 C. Method of determination: X-ray Diffraction

Crystal structure determination

a=5.24 Angstroem, b=6.62 Angstroem, c=8.73 Angstroem.; Temperature: 228 K. Method of determination: X-ray Diffraction

Cromer, Don T.; Ryan, Robert R.; Schiferl, David; Journal of Physical Chemistry; vol. 89; nb. 11; (1985); p. 2315 - 2318, View in Reaxys

Crystal structure determination

a=5.23 Angstroem, b=6.29 Angstroem, c=8.66 Angstroem, n=4.; Temperature: -60 C. Method of determination: Single Crystal X-ray Diffraction

Bagryanskaya, Yu. i.; Gatilov, Yu. V.; Journal of Structural Chemistry; vol. 24; nb. 1; (1983); p. 150 - 151; Zhurnal Strukturnoi Khimii; vol. 24; nb. 1; (1983); p. 158 - 160, View in Reaxys

Crystal structure determination

a=5.24 Angstroem, b=6.32 Angstroem, c=8.73 Angstroem, n=4.; Temperature: 4.2 K. Method of determination: Single Crystal X-ray Diffraction

Trevino, S. F.; Prince, E.; Hubbard, C. R.; Journal of Chemical Physics; vol. 73; nb. 6; (1980); p. 2996 - 3000, View in Reaxys

Solid state structure properties

Cromer, Don T.; Ryan, Robert R.; Schiferl, David; Journal of Physical Chemistry; vol. 89; nb. 11; (1985); p. 2315 - 2318, View in Reaxys

Harris; Journal of Chemical Physics; vol. 58; (1973); p. 5615, View in Reaxys

Crystal System (2)

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Crystal System

References

tetragonal

Cromer, Don T.; Ryan, Robert R.; Schiferl, David; Journal of Physical Chemistry; vol. 89; nb. 11; (1985); p. 2315 - 2318, View in Reaxys

rhombic

Bagryanskaya, Yu. i.; Gatilov, Yu. V.; Journal of Structural Chemistry; vol. 24; nb. 1; (1983); p. 150 - 151; Zhurnal Strukturnoi Khimii; vol. 24; nb. 1; (1983); p. 158 - 160, View in Reaxys; Trevino, S. F.; Prince, E.; Hubbard, C. R.; Journal of Chemical Physics; vol. 73; nb. 6; (1980); p. 2996 - 3000, View in Reaxys

Decomposition (2) 1 of 2

Decomposition [°C]

159.85

Solvent (Decomposition) neat (no solvent) Piermarini, G. J.; Block, S.; Miller, P. J.; Journal of Physical Chemistry; vol. 93; nb. 1; (1989); p. 457 - 462, View in Reaxys 2 of 2

Ornellas; Journal of Physical Chemistry; vol. 72; (1968); p. 2390, View in Reaxys; Borisov et al.; Kinetics and Catalysis; vol. 7; (1966); p. 521; ; p. 585, View in Reaxys

Dielectric Constant (11) Dielectric ConFrequency (Diestant lectric Constant) [Hz]

Temperature (Die- Comment (Dielec- References lectric Constant) tric Constant) [°C]

39.4

36.16

Rohani; Horne; Murthy; Organic Process Research and Development; vol. 9; nb. 6; (2005); p. 858 - 872, View in Reaxys 2E+06

Laurence, Christian; Nicolet, Pierre; Dalati, M. Tawfik; Abboud, Jose-Luis M.; Notario, Rafael; Journal of Physical Chemistry; vol. 98; nb. 23; (1994); p. 5807 - 5816, View in Reaxys Schlossarczyk,H. et al.; Helvetica Chimica Acta; vol. 56; (1973); p. 875 - 944, View in Reaxys; Chabrier,P. et al.; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 263; (1966); p. 1168 1171, View in Reaxys; Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 46; (1903); p. 174; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 54; (1906); p. 163, View in Reaxys; Schlundt; Chem. Zentralbl.; vol. 73; nb. I; (1902); p. 3, View in Reaxys; Maquestian et al.; Bulletin des Societes Chimiques Belges; vol. 80; (1971); p. 17,22, View in Reaxys; Suryanarayana; Somasundaram; Acta Chimica Academiae Scientiarum Hungaricae; vol. 24; (1960); p. 31,51, View in Reaxys; Gutmann; Schmid; Monatshefte fuer Chemie; vol. 100; (1969); p. 2113,2118, View in Reaxys; Shikhmamedbekova et al.; Zhurnal Organicheskoi Khimii; vol. 7; (1971); p. 870,885,886,887, View in Reaxys; Hanson et al.; Journal of Applied Chemistry and Biotechnology; vol. 25; (1975); p. 727,728, View in Reaxys; Chastrette; Tetrahedron; vol. 35; (1979); p. 1441,1442, View in Reaxys; Khimenko et al.; Russian Journal of Physical Chemistry; vol. 49; (1975); p. 1407; ; p. 2400, View in Reaxys; Papp et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 43; (1973); p. 171,168,170, View in Reaxys; Gutmann; Chimia; vol. 31; (1977); p. 1,2, View in Reaxys; Hudson; Loveday; Journal of the Chemical Society [Section] B: Physical Organic; (1966); p. 766,768, View in Reaxys; Luzkii; Obuchowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 2692,2512; Chem.Abstr.; vol. 57; nb. 64; (1962), View in Reaxys; Hartmann; Schmidt; Berichte der Bunsen-Gesellschaft; vol. 72; (1968); p. 875, View in Reaxys; Decroocq; Jungers; Comptes

90/412

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Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 252; (1961); p. 1454,1455, View in Reaxys; Neyens; Bulletin de la Societe Chimique de France; (1961); p. 720, View in Reaxys; Ramshaw et al.; Journal of Chemical Physics; vol. 54; (1971); p. 1239,1244, View in Reaxys; Zboinski et al.; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 27; (1979); p. 85,87,91, View in Reaxys; Regis; Corset; Canadian Journal of Chemistry; vol. 51; (1973); p. 3577,3582, 3584, 3585, View in Reaxys; Weisbecker; Rouquie; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 68; (1971); p. 910, View in Reaxys; Vsetecka; Exner; Collection of Czechoslovak Chemical Communications; vol. 39; (1974); p. 1140,1143, 1147, View in Reaxys; Dubenko et al.; Sov. Prog. Chem. (Engl. Transl.); vol. 42; nb. 6; (1976); p. 603,41,42, View in Reaxys; Abraham; Journal of the Chemical Society [Section] B: Physical Organic; (1971); p. 299,305, View in Reaxys; Dickinson et al.; Journal of Inorganic and Nuclear Chemistry; vol. 37; (1975); p. 511,515, View in Reaxys; Honda; Sasada; Japanese Journal of Applied Physics; vol. 16; (1977); p. 1775,1776-1778, View in Reaxys; Malarski; Roczniki Chemii; vol. 48; (1974); p. 663,666, View in Reaxys; Levin et al.; Russian Journal of Physical Chemistry; vol. 45; (1971); p. 1333, View in Reaxys; Tarnawski; Monatshefte fuer Chemie; vol. 93; (1962); p. 884,887, View in Reaxys; Martin et al.; Journal of Chemical Research, Synopses; (1979); p. 408, View in Reaxys; Cardaci et al.; Journal of Organometallic Chemistry; vol. 23; (1970); p. 265,272, View in Reaxys 3.36 - 35.5

-156.5 - -28.5

Philippe; Piette; Bulletin des Societes Chimiques Belges; vol. 64; (1955); p. 600,623, View in Reaxys

46.6 - 38.6

-25 - 20

Philippe; Piette; Bulletin des Societes Chimiques Belges; vol. 64; (1955); p. 600,623, View in Reaxys

38.2

Moll; Koll.Beih.; vol. 49; (1939); p. 7, View in Reaxys

40.4

Ostwald; Kolloid-Zeitschrift; vol. 45; (1928); p. 72, View in Reaxys

1.02

99.9

Pohrt; Annalen der Physik (Weinheim, Germany); vol. <4>42; (1913); p. 581, View in Reaxys

39.4

Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 70; (1910); p. 575, View in Reaxys

44.8

1.5

Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 70; (1910); p. 575, View in Reaxys

38.55 - 27.67

12 - 91

Dissociation Energy (5) Dissociation EnBond Type ergy [Jmol-1]

References

407794

C-H

Static Dielectric constant:λ= 90.0 bis 217.8 m.

Lattey; Gatty; Phil.Mag.; vol. <7>7; p. 1000, View in Reaxys

Bordwell, F. G.; Zhao, Yongyu; Journal of Organic Chemistry; vol. 60; nb. 20; (1995); p. 6348 - 6352, View in Reaxys

91/412

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410306

C-H

Bordwell, F. G.; Harrelson, John A.; Zhang, Xianman; Journal of Organic Chemistry; vol. 56; nb. 14; (1991); p. 4448 - 4450, View in Reaxys

266699

C-N

Chen, Edward C. M.; Albyn, Keith; Dussack, Laurie; Wentworth, W. E.; Journal of Physical Chemistry; vol. 93; nb. 18; (1989); p. 6827 - 6832, View in Reaxys Cumming et al.; Canadian Journal of Chemistry; vol. 55; (1977); p. 3474,3477, View in Reaxys; Knobel et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 20; (1971); p. 425,426,427; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 20; (1971); p. 485, View in Reaxys; Timotcheus et al.; Reaktsionnaya Sposobnost Organicheskikh Soedinenii; vol. 2; nb. 2; (1965); p. 16,22, View in Reaxys; Esikova et al.; Russian Journal of Physical Chemistry; vol. 50; (1976); p. 404; ; p. 692, View in Reaxys

CH3-NO2

Kandel; Journal of Chemical Physics; vol. 23; (1955); p. 84,85, View in Reaxys; Gray; Transactions of the Faraday Society; vol. 51; (1955); p. 1367,1368, View in Reaxys

Dissociation Exponent (44) 1 of 44

Dissociation Exponent (pK)

17.2

Solvent (Dissociation Exponent)

dimethylsulfoxide

Type (Dissociation Exponent)

a1/apparent

Xu, Chunli; Bartley, Jonathan K.; Enache, Dan I.; Knight, David W.; Hutchings, Graham J.; Synthesis; nb. 19; (2005); p. 3468 - 3476; Art.No: C08805SS, View in Reaxys 2 of 44

Dissociation Exponent (pK)

10.7

Dissociation Group

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

H2O

Method (Dissociation Exponent)

spectrophotometric

Type (Dissociation Exponent)

a3/apparent

Bernasconi, Claude F.; Panda, Markandeswar; Stronach, Michael W.; Journal of the American Chemical Society; vol. 117; nb. 36; (1995); p. 9206 - 9212, View in Reaxys 3 of 44

Type (Dissociation Exponent)

a1/apparent

Bordwell, Frederick G.; Satish; Journal of the American Chemical Society; vol. 116; nb. 20; (1994); p. 8885 - 8889, View in Reaxys 4 of 44

Dissociation Exponent (pK)

10.28

Dissociation Group

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

H2O

Method (Dissociation Exponent)

spectrophotometric

Type (Dissociation Exponent)

a1/thermodynamic

Bernasconi, Claude F.; Kliner, Dahv A.; Mullin, Amy S.; Ni, Jiu Xiang; Journal of Organic Chemistry; vol. 53; nb. 14; (1988); p. 3342 - 3351, View in Reaxys 5 of 44

Dissociation Exponent (pK)

11.32

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Dissociation Group

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

dimethylsulfoxide; H2O

Method (Dissociation Exponent)

spectrophotometric

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 50percent

Bernasconi, Claude F.; Kliner, Dahv A.; Mullin, Amy S.; Ni, Jiu Xiang; Journal of Organic Chemistry; vol. 53; nb. 14; (1988); p. 3342 - 3351, View in Reaxys 6 of 44

Dissociation Exponent (pK)

12.44

Dissociation Group

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

dimethylsulfoxide; H2O

Method (Dissociation Exponent)

spectrophotometric

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 70percent

Bernasconi, Claude F.; Kliner, Dahv A.; Mullin, Amy S.; Ni, Jiu Xiang; Journal of Organic Chemistry; vol. 53; nb. 14; (1988); p. 3342 - 3351, View in Reaxys 7 of 44

Dissociation Exponent (pK)

14.8

Dissociation Group

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

dimethylsulfoxide; H2O

Method (Dissociation Exponent)

spectrophotometric

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 90percent

Bernasconi, Claude F.; Kliner, Dahv A.; Mullin, Amy S.; Ni, Jiu Xiang; Journal of Organic Chemistry; vol. 53; nb. 14; (1988); p. 3342 - 3351, View in Reaxys 8 of 44

Dissociation Exponent (pK)

17.2

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

dimethylsulfoxide

Type (Dissociation Exponent)

a1/apparent

93/412

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Bordwell, Frederick G.; Branca, John C.; Hughes, David L.; Olmstead, William N.; Journal of Organic Chemistry; vol. 45; nb. 16; (1980); p. 3305 - 3313, View in Reaxys 9 of 44

Dissociation Exponent (pK)

19.8

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

various solvent(s)

Type (Dissociation Exponent)

a1/apparent

Bordwell, Frederick G.; Branca, John C.; Hughes, David L.; Olmstead, William N.; Journal of Organic Chemistry; vol. 45; nb. 16; (1980); p. 3305 - 3313, View in Reaxys 10 of 44

Dissociation Exponent (pK)

17.2

Dissociation Group

RCH-H

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

dimethylsulfoxide

Type (Dissociation Exponent)

a1/thermodynamic

Olmstead, William N.; Bordwell, Frederick G.; Journal of Organic Chemistry; vol. 45; nb. 16; (1980); p. 3299 3305, View in Reaxys 11 of 44

Dissociation Exponent (pK)

1.57

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

fluorosulfonic acid

Method (Dissociation Exponent)

conductometric

Type (Dissociation Exponent)

b1/apparent

Russell, David G.; Senior, John B.; Canadian Journal of Chemistry; vol. 58; nb. 1; (1980); p. 22 - 29, View in Reaxys 12 of 44

Dissociation Exponent (pK)

2.12

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

various solvent(s)

Method (Dissociation Exponent)

conductometric

Type (Dissociation Exponent)

b1/apparent

Russell, David G.; Senior, John B.; Canadian Journal of Chemistry; vol. 58; nb. 1; (1980); p. 22 - 29, View in Reaxys 13 of 44

Dissociation Exponent (pK)

2.6

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

H2SO4

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Method (Dissociation Exponent)

conductometric

Type (Dissociation Exponent)

b1/apparent

Russell, David G.; Senior, John B.; Canadian Journal of Chemistry; vol. 58; nb. 1; (1980); p. 22 - 29, View in Reaxys 14 of 44

Comment (Dissociation Exponent)

(pk')

Cumming et al.; Canadian Journal of Chemistry; vol. 55; (1977); p. 3474,3477, View in Reaxys; Ritchie; Uschold; Journal of the American Chemical Society; vol. 89; (1967); p. 1721,1723, View in Reaxys; Bidan et al.; Tetrahedron; vol. 35; (1979); p. 177,178, View in Reaxys 15 of 44

Comment (Dissociation Exponent)

(pk')pK(a)

Yur'ev et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 48; (1978); p. 149,128, View in Reaxys 16 of 44

Comment (Dissociation Exponent)

(pk')pK

Ritchie; Uschold; Journal of the American Chemical Society; vol. 89; (1967); p. 2752, View in Reaxys; Bordwell et al.; Journal of Organic Chemistry; vol. 43; (1978); p. 3095,3096, View in Reaxys; Bordwell et al.; Journal of Organic Chemistry; vol. 43; (1978); p. 3107,3108, View in Reaxys 17 of 44

Comment (Dissociation Exponent)

(k')K

Bordwell et al.; Journal of Organic Chemistry; vol. 43; (1978); p. 3107,3108, View in Reaxys 18 of 44

Comment (Dissociation Exponent)

(pk')pK: 17.2

Bordwell et al.; Journal of Organic Chemistry; vol. 42; (1977); p. 326,331, View in Reaxys 19 of 44

Comment (Dissociation Exponent)

(pk')pKa (Table I)

Spinner; Journal of Organic Chemistry; vol. 40; (1975); p. 3580,3581,3583, View in Reaxys 20 of 44

Comment (Dissociation Exponent)

(pk')der pK(S)-Wert bei Ritchie,Uschold,J.Am.Chem.Soc.89<1967>1721 ist um 2.1 zu niedrig angegeben

Matthews et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 7006,7007-7014, View in Reaxys 21 of 44

Comment (Dissociation Exponent)

(pk)absoluter pK(S)-Wert in DMSO

Matthews et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 7006,7007-7014, View in Reaxys 22 of 44

Comment (Dissociation Exponent)

(pk')pK(s)-Wert in DMSO

Bordwell,F.G. et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 7160 - 7162, View in Reaxys 23 of 44

Comment (Dissociation Exponent)

(pk')in waessriger Lsg.

Matsui; Hepler; Canadian Journal of Chemistry; vol. 51; (1973); p. 1941,1943, View in Reaxys 24 of 44

Comment (Dissociation Exponent)

(pk')pK(A) der Ionisierung

Crowell; Kim; Journal of the American Chemical Society; vol. 95; (1973); p. 6781,6782-6786, View in Reaxys 25 of 44

Comment (Dissociation Exponent)

(pk')pK(a) (Tab.1, S.1441)

Petrov; Bykova; J. Gen. Chem. USSR (Engl. Transl.); vol. 42; (1972); p. 1446,1438, View in Reaxys 26 of 44

Comment (Dissociation Exponent)

(pk')pK(BH+) (Tab.1, S.1441)

Petrov; Bykova; J. Gen. Chem. USSR (Engl. Transl.); vol. 42; (1972); p. 1446,1438, View in Reaxys 27 of 44

Comment (Dissociation Exponent)

(pk')pK (Acn.)

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Fedorov; Aksenenko; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 1166; ; p. 2040, View in Reaxys 28 of 44

Comment (Dissociation Exponent)

(pk')pK (Tributylphosphate)

Fedorov; Aksenenko; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 1166; ; p. 2040, View in Reaxys 29 of 44

Comment (Dissociation Exponent)

(pk')15,9 (in DMSO)

Bordwell; Quarterly Reports on Sulfur Chemistry; vol. 7; (1972); p. 187, View in Reaxys 30 of 44

Comment (Dissociation Exponent)

(k')Tabelle 6

Belikov et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 20; (1971); p. 272,275; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 20; (1971); p. 335, View in Reaxys 31 of 44

Comment (Dissociation Exponent)

(pk')pK(a) in DMSO

Faleev et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1970); p. 69; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1970); p. 73, View in Reaxys 32 of 44

Comment (Dissociation Exponent)

(k')K(Base) in CH3SO3H

Paul et al.; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1970); p. 2712, View in Reaxys 33 of 44

Comment (Dissociation Exponent)

(k')K(Base) in H2SO4

Paul et al.; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1970); p. 2712, View in Reaxys 34 of 44

Comment (Dissociation Exponent)

(k')K(Base) in HSO3F, Tab. 2

Paul et al.; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1970); p. 2712, View in Reaxys 35 of 44

Comment (Dissociation Exponent)

(pk')pK (DMF)

Fedorov et al.; Russian Journal of Physical Chemistry; vol. 43; (1969); p. 838; Zhurnal Fizicheskoi Khimii; vol. 43; (1969); p. 1508, View in Reaxys 36 of 44

Comment (Dissociation Exponent)

(pk')pK(a): 15.64

Belonkon' et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1969); p. 949,950,954; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1969); p. 1039, View in Reaxys 37 of 44

Comment (Dissociation Exponent)

(k')K(b) (H2SO4)

Gillespie; Malhotra; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1968); p. 1933,1934,1935,1936,1937, View in Reaxys 38 of 44

Comment (Dissociation Exponent)

(k')in Pufferloesungen

Timotcheus et al.; Reaktsionnaya Sposobnost Organicheskikh Soedinenii; vol. 2; nb. 2; (1965); p. 16,22, View in Reaxys 39 of 44

Comment (Dissociation Exponent)

(pk')(Temp. nicht angeg.) in Wasser, spektrophotometrisch ermittelt

Nowikow et al.; Tetrahedron, Supplement; vol. 6; (1964); p. 119,128; Chem.Abstr.; nb. 14665; (1965), View in Reaxys 40 of 44

Solvent (Dissociation Exponent)

H2SO4

Method (Dissociation Exponent)

conductometric

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Type (Dissociation Exponent)

thermodynamic

Gillespie; Solomons; Journal of the Chemical Society; (1957); p. 1796,1797, 1802, View in Reaxys 41 of 44

Dissociation Exponent (pK)

3.22

Temperature (Dissociation Exponent) [°C]

Type (Dissociation Exponent)

apparent

Comment (Dissociation Exponent)

wahre Dissoziationskonstante K:aci-Form.

Junell zit bei Turnbull;Maron; Journal of the American Chemical Society; vol. 65; (1943); p. 214, View in Reaxys 42 of 44

Dissociation Exponent (pK)

10.45

Temperature (Dissociation Exponent) [°C]

Type (Dissociation Exponent)

apparent

Comment (Dissociation Exponent)

wahre Dissoziationskonstante K:Nitro-Form.

Wheland; Farr; Journal of the American Chemical Society; vol. 65; p. 1433, View in Reaxys; Turnbull; Maron; Journal of the American Chemical Society; vol. 65; (1943); p. 214,215, View in Reaxys 43 of 44

Dissociation Exponent (pK)

10.33

Temperature (Dissociation Exponent) [°C]

Type (Dissociation Exponent)

apparent

Comment (Dissociation Exponent)

wahre Dissoziationskonstante K:Nitro-Form.

Dissociation Exponent (pK)

10.21

Temperature (Dissociation Exponent) [°C]

Type (Dissociation Exponent)

apparent

Comment (Dissociation Exponent)

wahre Dissoziationskonstante K:Nitro-Form.

References

0.006313

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys

0.006205

Lorenzi, Lorenzo De; Fermeglia, Maurizio; Torriano, Giovanni; Journal of Chemical & Engineering Data; vol. 40; nb. 6; (1995); p. 1172 - 1177, View in Reaxys

0.0063

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2016-04-19 03:35:30

0.00621

Skomorokhov, V. I.; Dregalin, A. F.; Russian Journal of Physical Chemistry; vol. 66; nb. 11; (1992); p. 1569 - 1572; Zhurnal Fizicheskoi Khimii; vol. 66; (1992); p. 2947 - 2953, View in Reaxys

0.00644

Yadava, Raja R.; Yadava, Sarvanand S.; Singh, Vishwa N.; Journal of Chemical & Engineering Data; vol. 33; nb. 4; (1988); p. 402 - 404, View in Reaxys

0.00627

Wright; Murray-Rust; Hartley; Journal of the Chemical Society; (1931); p. 202, View in Reaxys; Manjeshwar, Lata S.; Aminabhavi, Tejraj M.; Journal of Chemical & Engineering Data; vol. 32; nb. 4; (1987); p. 409 - 412, View in Reaxys

0.627

Aminabhavi, T. M.; Manjeshwar, L. S.; Balundgi, R. H.; Journal of Chemical & Engineering Data; vol. 32; nb. 1; (1987); p. 50 - 52, View in Reaxys

0.005187

Manjeshwar, Lata S.; Aminabhavi, Tejraj M.; Journal of Chemical & Engineering Data; vol. 32; nb. 4; (1987); p. 409 - 412, View in Reaxys

0.00622

Udowenko; Chomenko; Zhurnal Obshchei Khimii; vol. 27; (1957); p. 583; engl. Ausg. S. 649, View in Reaxys

0.00485

Udowenko; Chomenko; Zhurnal Obshchei Khimii; vol. 27; (1957); p. 583; engl. Ausg. S. 649, View in Reaxys

0.00399

Udowenko; Chomenko; Zhurnal Obshchei Khimii; vol. 27; (1957); p. 583; engl. Ausg. S. 649, View in Reaxys

0.00646

Thompson et al.; Journal of the American Chemical Society; vol. 76; (1954); p. 3445, View in Reaxys

0.00608

Thompson et al.; Journal of the American Chemical Society; vol. 76; (1954); p. 3445, View in Reaxys

0.00574

Thompson et al.; Journal of the American Chemical Society; vol. 76; (1954); p. 3445, View in Reaxys

0.00619

Maclay; Fuoss; Journal of Polymer Science; vol. 6; (1951); p. 511,513, View in Reaxys

0.00632

Holcomb; Dorsey; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2788, View in Reaxys

0.00748

Bellinger et al.; Industrial and Engineering Chemistry; vol. 40; (1948); p. 1320, View in Reaxys

0.00625

Bellinger et al.; Industrial and Engineering Chemistry; vol. 40; (1948); p. 1320, View in Reaxys

0.00533

Bellinger et al.; Industrial and Engineering Chemistry; vol. 40; (1948); p. 1320, View in Reaxys

0.00322 0.00692

16.4 - 96.3

Friend; Hargreaves; Phil.Mag.; vol. <7>34; (1943); p. 814, View in Reaxys

0.008533

Walden; Birr; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 163; (1933); p. 273,335, View in Reaxys

0.0062

Walden; Birr; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 163; (1933); p. 273,335, View in Reaxys

0.00478

Walden; Birr; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 163; (1933); p. 273,335, View in Reaxys

0.00697

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 558, View in Reaxys

0.00595

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 558, View in Reaxys

0.00343 0.00844

0 - 85

Philip; Oakley; Journal of the Chemical Society; vol. 125; (1924); p. 1194, View in Reaxys

Electrical Data (11) 1 of 11

Description (Electrical Data)

Electrical conductivity

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Miller; Fuoss; Journal of the American Chemical Society; vol. 75; (1953); p. 3076,3079, View in Reaxys; Philip; Courtman; Journal of the Chemical Society; vol. 97; (1910); p. 1265, View in Reaxys; Wright; Murray-Rust; Hartley; Journal of the Chemical Society; (1931); p. 202, View in Reaxys; Baessler; Riehl; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 20; (1965); p. 587, View in Reaxys; Paul et al.; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1970); p. 2712, View in Reaxys; Soffer; Folmann; Transactions of the Faraday Society; vol. 62; (1966); p. 3559,3562, View in Reaxys; Heubel et al.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 15; (1977); p. 687, View in Reaxys; Little; Singleterry; Journal of Physical Chemistry; vol. 68; (1964); p. 2709, View in Reaxys; Peach; Waddington; Journal of the Chemical Society; (1962); p. 2680,2681, View in Reaxys; Potts; Walker; Canadian Journal of Chemistry; vol. 49; (1971); p. 2171, View in Reaxys; Owensby et al.; Journal of the American Chemical Society; vol. 96; (1974); p. 2682,2684,2685,2686, View in Reaxys; Gillespie; Accounts of Chemical Research; vol. 1; (1968); p. 202,203, View in Reaxys; Andrade et al.; Inorganica Chimica Acta; vol. 19; (1976); p. L19, View in Reaxys; Matrosov et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 25; (1976); p. 295,298; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 25; (1976); p. 313, View in Reaxys; Gillespie; Malhotra; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1968); p. 1933,1934,1935,1936,1937, View in Reaxys; Pawlak; Roczniki Chemii; vol. 46; (1972); p. 2069, View in Reaxys; Dutta et al.; Inorganic Chemistry; vol. 9; (1970); p. 1215,1216, View in Reaxys; Casey et al.; Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999); (1974); p. 886,887, View in Reaxys; Jarosiewicz; Szychlinski; Roczniki Chemii; vol. 48; (1974); p. 1545,1546, 1548, 1550, View in Reaxys; Russell, David G.; Senior, John B.; Canadian Journal of Chemistry; vol. 58; nb. 1; (1980); p. 22 29, View in Reaxys 2 of 11

Description (Electrical Data)

Dielectric saturation

Zboinski; Journal of Chemical Physics; vol. 63; (1975); p. 1698, View in Reaxys 3 of 11

Description (Electrical Data)

Photoconductivity

Jarosiewicz; Szychlinski; Roczniki Chemii; vol. 48; (1974); p. 1545,1546, 1548, 1550, View in Reaxys 4 of 11

Description (Electrical Data)

Dielectric loss

Levin et al.; Russian Journal of Physical Chemistry; vol. 45; (1971); p. 1333, View in Reaxys 5 of 11

Description (Electrical Data)

Dielectric relaxation time

Clark; Kumer; Brit.J.appl.Physics; vol. 7; (1956); p. 282, View in Reaxys; Le Fevre; Sullivan; Journal of the Chemical Society; (1954); p. 2873,2876, View in Reaxys; Chandra; Nath; Bulletin of the Chemical Society of Japan; vol. 43; (1970); p. 1614, View in Reaxys 6 of 11

Description (Electrical Data)

Electrical properties

Krishnamurthy; Soundararajan; Indian Journal of Chemistry; vol. 3; (1965); p. 479, View in Reaxys; Quinn; Smyth; Journal of Chemical Physics; vol. 41; (1964); p. 2037, View in Reaxys 7 of 11

Description (Electrical Data)

Dielectric loss

Comment (Electrical Da- in binaeren Gemischen mit Tetrachlormethan und Benzol im Mikrowellen-Bereich (0.86 ta) cm) bei 10-40grad. Clark; Kumer; Brit.J.appl.Physics; vol. 7; (1956); p. 282, View in Reaxys 8 of 11

Description (Electrical Data)

Electrical conductivity

Comment (Electrical Da- Diagramm des Systems mit Aluminiumchlorid. ta) Galinker; Zhurnal Obshchei Khimii; vol. 26; (1956); p. 1564,1565;engl.Ausg.S.1753, View in Reaxys 9 of 11

Description (Electrical Data)

Electrical conductivity

Comment (Electrical Da- und Dielektrizitaetskonstante von Gemischen mit Methanol. ta) Miller; Fuoss; Journal of the American Chemical Society; vol. 75; (1953); p. 3076,3079, View in Reaxys 10 of 11

Description (Electrical Data)

Dielectric loss

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Comment (Electrical Da- in Benzol und Relaxationszeit im Bereich der Mikrowellen bei ca.19grad (λ=1.27 und 3.26 ta) cm). Whiffen; Thompson; Transactions of the Faraday Society; vol. 42 A; (1946); p. 118; Chem.Abstr.; (1949); p. 6018, View in Reaxys 11 of 11

Description (Electrical Data)

Dielectric loss

Comment (Electrical Da- in Benzol und Relaxationszeit im Bereich der Mikrowellen bei ca.18.5+-1grad (λ=1.25 und ta) 3.25 cm). Cripwell; Sutherland; Transactions of the Faraday Society; vol. 42 A; (1946); p. 151; Chem.Abstr.; (1949); p. 6019, View in Reaxys Electrical Moment (30) 1 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.46

Temperature (Electrical Moment) [°C]

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 2 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

2.7

Borovikov; Makovetskii; Pivovarova; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 100; nb. 1; (1996); p. 33 - 38, View in Reaxys 3 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.52

Cox, A. P.; Journal of Molecular Structure; vol. 97; (1983); p. 61 - 76, View in Reaxys 4 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.32

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (ε)

Solvent (Electrical Moment)

cyclohexane

Yadava, R. R.; Singh, V. N.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical; vol. 21; nb. 1; (1982); p. 17 - 19, View in Reaxys 5 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.41

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (ε)

Solvent (Electrical Moment)

1,3,5-trimethyl-benzene

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Yadava, R. R.; Singh, V. N.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical; vol. 21; nb. 1; (1982); p. 17 - 19, View in Reaxys 6 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.45

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (ε)

Solvent (Electrical Moment)

xylene

Yadava, R. R.; Singh, V. N.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical; vol. 21; nb. 1; (1982); p. 17 - 19, View in Reaxys 7 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.52

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (ε)

Solvent (Electrical Moment)

benzene

Yadava, R. R.; Singh, V. N.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical; vol. 21; nb. 1; (1982); p. 17 - 19, View in Reaxys 8 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.5

Temperature (Electrical Moment) [°C]

19.9

Solvent (Electrical Moment)

benzene

Balakier, Grazyna; Polish Journal of Chemistry; vol. 54; nb. 11/12; (1980); p. 2297 - 2304, View in Reaxys 9 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.5

Temperature (Electrical Moment) [°C]

293

Solvent (Electrical Moment)

CCl4

Balakier, Grazyna; Polish Journal of Chemistry; vol. 54; nb. 11/12; (1980); p. 2297 - 2304, View in Reaxys 10 of 30

Description (Electrical Moment)

Dipole moment

Nelson et al.; Journal of Physical Chemistry; vol. 71; (1967); p. 2742, View in Reaxys; Exner; Vsetecka; Tetrahedron Letters; (1972); p. 4613, View in Reaxys; Mauret et al.; Bulletin de la Societe Chimique de France; (1974); p. 379, View in Reaxys; Belik et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 25; (1976); p. 1619,1620,1621; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 25; (1976); p. 1714, View in Reaxys; Barth et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1979); p. 907,908, View in Reaxys; Vysotskii; Journal of Structural Chemistry; vol. 19; (1978); p. 27,31; ; p. 34, View in Reaxys; Vsetecka; Exner; Collection of Czechoslovak Chemical Communications; vol. 39; (1974); p. 1140,1143, 1147, View in Reaxys; Osipov et al.; Bulletin of the Academy of Sciences of

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the USSR, Division of Chemical Science (English Translation); vol. 25; (1976); p. 677; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 25; (1976); p. 688, View in Reaxys; Kuhn et al.; Helvetica Chimica Acta; vol. 54; (1971); p. 2260,2265-2266, 2273-2274, View in Reaxys; Martin et al.; Journal of Chemical Research, Synopses; (1979); p. 408, View in Reaxys 11 of 30

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

Weisbecker; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 274; (1972); p. 451,453, View in Reaxys; Hanson et al.; Journal of Applied Chemistry and Biotechnology; vol. 25; (1975); p. 727,728, View in Reaxys; Chastrette; Tetrahedron; vol. 35; (1979); p. 1441,1442, View in Reaxys; Bieri; Heilbronner; Helvetica Chimica Acta; vol. 57; (1974); p. 546,547, 548, View in Reaxys; Sakodynsky et al.; Analytical Chemistry; vol. 45; (1973); p. 1369,1372, View in Reaxys; Zboinski et al.; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 27; (1979); p. 85,87,91, View in Reaxys; Weisbecker; Rouquie; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 68; (1971); p. 910, View in Reaxys; Polezzo; Simonetta; Chemical Physics Letters; vol. 1; (1967); p. 85, View in Reaxys; Chandra; Nath; Bulletin of the Chemical Society of Japan; vol. 43; (1970); p. 1614, View in Reaxys; Malarski; Roczniki Chemii; vol. 48; (1974); p. 663,666, View in Reaxys 12 of 30

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

S. 1619

Diggle; Parker; Australian Journal of Chemistry; vol. 27; (1974); p. 1617,1619, 1620, View in Reaxys 13 of 30

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

Mischung m. Acn.: μ

Lutskii et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 43; (1973); p. 2597,2578,2579, View in Reaxys 14 of 30

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

Table 1

Exner; Vsetecka; Tetrahedron Letters; (1972); p. 4613, View in Reaxys 15 of 30

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

Volumenfraktion, Polarisierung

Borovikov; Egorov; Theoretical and Experimental Chemistry; vol. 7; (1971); p. 539,540; ; p. 251, View in Reaxys 16 of 30

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

μ; τ(Dipol)

Boldeskul et al.; Optics and Spectroscopy; vol. 29; (1970); p. 142; ; p. 270, View in Reaxys 17 of 30

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

der Bindung

Singh; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 23; (1967); p. 439,444, View in Reaxys 18 of 30

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

ε; Dioxan+Ethylencarbonat : bei 25grad: 3.26D bzw. 3.27D

Myers; Sun; Journal of Physical Chemistry; vol. 70; (1966); p. 3217,3221, View in Reaxys

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19 of 30

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

3.15 D

Kinugasa; Nakashima; Nippon Kagaku Zasshi; vol. 86; (1965); p. 497; Chem.Abstr.; vol. 63; nb. 5506; (1965), View in Reaxys 20 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.43

Method (Electrical Moment)

Dielectric constant (ε)

Solvent (Electrical Moment)

benzene

Buckingham; Raab; Transactions of the Faraday Society; vol. 55; (1959); p. 377,384, View in Reaxys; Campbell; Hall; Pr.W.Virginia Acad.; vol. 23; (1951); p. 64,67, View in Reaxys 21 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.53

Method (Electrical Moment)

Dielectric constant (ε)

Comment (Electrical Moment)

Dipolmoment::der Fluessigkeit.

Osipow; Zhurnal Fizicheskoi Khimii; vol. 31; (1957); p. 1542,1544; Chem.Abstr.; (1958); p. 5911, View in Reaxys 22 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.46

Method (Electrical Moment)

Microwave absorption

Comment (Electrical Moment)

Dipolmoment::der Fluessigkeit.

Tannenbaum et al.; Journal of Chemical Physics; vol. 25; (1956); p. 42,44, View in Reaxys 23 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.43

Method (Electrical Moment)

Dielectric constant (ε)

Comment (Electrical Moment)

Dipolmoment::des Dampfes.

Le Fevre; Rao; Australian Journal of Chemistry; vol. 7; (1954); p. 135,144, View in Reaxys 24 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.5

Comment (Electrical Moment)

at:68-223 degreeC.

Smyth; McAlpine; Journal of the American Chemical Society; vol. 56; (1934); p. 1698, View in Reaxys; Smyth; Journal of the American Chemical Society; vol. 63; (1941); p. 58, View in Reaxys

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25 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.54

Comment (Electrical Moment)

at:64-181 degreeC.

Cripwell; Sutherland; Journal of the Chemical Society; (1937); p. 162, View in Reaxys 26 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.1

Temperature (Electrical Moment) [°C]

Solvent (Electrical Moment)

benzene

van Arkel; Snoek; Transactions of the Faraday Society; Phys.Z.; vol. 35; (1934); p. 712,189, View in Reaxys 27 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.1

Temperature (Electrical Moment) [°C]

Solvent (Electrical Moment)

CCl4

van Arkel; Snoek; Transactions of the Faraday Society; Phys.Z.; vol. 35; (1934); p. 712,189, View in Reaxys 28 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.02

Temperature (Electrical Moment) [°C]

Solvent (Electrical Moment)

benzene

Hunter; Partington; Journal of the Chemical Society; (1933); p. 312, View in Reaxys 29 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.13

Temperature (Electrical Moment) [°C]

Solvent (Electrical Moment)

benzene

Weissberger; Saengewald; Chemische Berichte; vol. 65; (1932); p. 703, View in Reaxys 30 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.05

Solvent (Electrical Moment)

benzene

Hoejendahl; Phys.Z.; vol. 30; (1929); p. 394, View in Reaxys Electrical Polarizability (3)

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Description (Elec- References trical Polarizability) Molar polarization Ponomarenko, S. M.; Mushtakova, S. P.; Demakhin, A. G.; Faifel', B. L.; Kal'manovich, D. G.; Russian Journal of General Chemistry; vol. 65; nb. 2.1; (1995); p. 160 - 167; Zhurnal Obshchei Khimii; vol. 65; nb. 2; (1995); p. 190 - 198, View in Reaxys Atom polarization

Rao; Thyagarajan; Indian Journal of Pure and Applied Physics; vol. 12; (1974); p. 242, View in Reaxys

Optical anisotropy Malmberg; Lippincott; Journal of Colloid and Interface Science; vol. 27; (1968); p. 591,598,606, View in Reaxys Electrochemical Behaviour (11) Description (Elec- Comment (Electrochemical Betrochemical Behaviour) haviour)

References

Electrolytic dissociation / protonation equilibrium

Olmstead, William N.; Bordwell, Frederick G.; Journal of Organic Chemistry; vol. 45; nb. 16; (1980); p. 3299 - 3305, View in Reaxys; Bordwell, Frederick G.; Branca, John C.; Hughes, David L.; Olmstead, William N.; Journal of Organic Chemistry; vol. 45; nb. 16; (1980); p. 3305 - 3313, View in Reaxys; Wentworth, W.E.; Batten, C.F.; D'Sa, E.Desai; Chen, E.C.M.; Journal of Physical Chemistry; vol. 98; nb. 46; (1994); p. 11902 11908, View in Reaxys; Bordwell, Frederick G.; Satish; Journal of the American Chemical Society; vol. 116; nb. 20; (1994); p. 8885 - 8889, View in Reaxys; Bordwell, F. G.; Zhao, Yongyu; Journal of Organic Chemistry; vol. 60; nb. 20; (1995); p. 6348 - 6352, View in Reaxys; Arai, Shigeru; Nakayama, Keiji; Ishida, Toshimasa; Shioiri, Takayuki; Tetrahedron Letters; vol. 40; nb. 22; (1999); p. 4215 - 4218, View in Reaxys

Enthalpy of disso- Enthalpy: 24702 ciation (electrolyt- J/mol. Temperaic) / protonation ture: 24 deg C.

Wilson, Burton; Georgiadis, Rosina; Bartmess, John E.; Journal of the American Chemical Society; vol. 113; nb. 5; (1991); p. 1762 - 1766, View in Reaxys

Thermodynamic parameters for dissociation / protonation

Arnett, Edward M.; Venkatasubramaniam, K. G.; Journal of Organic Chemistry; vol. 48; nb. 10; (1983); p. 1569 - 1578, View in Reaxys

Proton affinity

McAllister; Pitman; International Journal of Mass Spectrometry and Ion Physics; vol. 19; (1976); p. 241, View in Reaxys; Mackay; Bohme; International Journal of Mass Spectrometry and Ion Physics; vol. 26; (1978); p. 327,331, 333, 337, View in Reaxys

Acidity

Streuli; Analytical Chemistry; vol. 32; (1960); p. 407,408, View in Reaxys; Cumming; Kebarle; Canadian Journal of Chemistry; vol. 56; (1978); p. 1,5, View in Reaxys; Nesterchuk et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 48; (1975); p. 2715,2795,2796, View in Reaxys; Bordwell; Matthews; Journal of the American Chemical Society; vol. 96; (1974); p. 1216, View in Reaxys; Kreshkov et al.; J. Anal. Chem. USSR (Engl. Transl.); vol. 23; (1968); p. 271,222, View in Reaxys; Petrov; Bykova; J. Gen. Chem. USSR (Engl. Transl.); vol. 42; (1972); p. 1446,1438, View in Reaxys; Kreshkov et al.; J. Anal. Chem. USSR (Engl. Transl.); vol. 24; (1969); p. 1453,1177,1178, View in Reaxys; Cumming; Kebarle; Journal of the American Chemical Society; vol. 100; (1978); p. 1835,1836, View in Reaxys

Electrochemical properties

Shcherev et al.; Russian Journal of Physical Chemistry; vol. 39; (1965); p. 917; ; p. 1733, View in Reaxys; Lopez Teijelo et al.; Anales de la Asociacion Quimica Argentina (1921-2001); vol. 66; (1978); p. 333, View in Reaxys; Guidelli; Foresti; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 88; (1978); p. 65, View in Reaxys; Glushchenko; Radaev; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 27; (1978); p. 463; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 27; (1978); p. 538, View in Reaxys; Matrosov et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 25; (1976); p. 295,298; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 25; (1976); p. 313, View in Reaxys; Diggle; Parker; Australian Journal of Chemistry; vol. 27; (1974); p. 1617,1619, 1620, View in Reaxys

Autoprotolysis

Kozachenko et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 25; (1976); p. 2275; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 25; (1976); p. 2440, View in Reaxys

Enthalpy of disso- . ciation (electrolytic) / protonation

Matsui; Hepler; Canadian Journal of Chemistry; vol. 51; (1973); p. 1941,1943, View in Reaxys

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Kinetics of dissociation (electrolytic) / protonation

Matsui; Hepler; Canadian Journal of Chemistry; vol. 51; (1973); p. 1941,1943, View in Reaxys; Sargla et al.; Organic Reactivity (New York, English Translation); vol. 3; (1966); p. 180, View in Reaxys

Basicity

Petrov; Bykova; J. Gen. Chem. USSR (Engl. Transl.); vol. 42; (1972); p. 1446,1438, View in Reaxys

Polarography

Tur'jan; Tmekalowa; J. Appl. Chem. USSR (Engl. Transl.); vol. 35; (1962); p. 2729,2618; Chem.Abstr.; vol. 59; nb. 2605; (1963), View in Reaxys; Malinowskii et al.; Sov. Prog. Chem. (Engl. Transl.); vol. 34; nb. 11; (1968); p. 1202,99, View in Reaxys; Suzuki; Elving; Collection of Czechoslovak Chemical Communications; vol. 25; (1960); p. 3202, View in Reaxys; Kurochkina; Kedrinskii; J. Appl. Chem. USSR (Engl. Transl.); vol. 43; (1970); p. 341,347, View in Reaxys

Electrochemical Characteristics (15) 1 of 15

Description (Electrochemical Characteristics)

voltammetry

Solvent (Electrochemical Characteristics)

neat liquid

Temperature (Electrochemical Characteristics) [°C]

-10 - 50

Caban, Karolina; Donten, Mikolaj; Stojek, Zbigniew; Journal of Physical Chemistry B; vol. 108; nb. 3; (2004); p. 1153 - 1159, View in Reaxys 2 of 15

Description (Electrochemical Characteristics)

polarographic half-wave potential

Tribalat; Grall; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 274; (1972); p. 1888,1889-1891, View in Reaxys; Kargin et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 47; (1977); p. 166,153,155,156, View in Reaxys; Aixill, W. Joanne; Mills, Peter B.; Compton, Richard G.; Prieto, Francisco; Rueda, Manuela; Journal of Physical Chemistry B: Condensed Matter, Materials, Surfaces, Interfaces, & Biophysical Chemistry; vol. 102; nb. 46; (1998); p. 9187 - 9190, View in Reaxys 3 of 15

Description (Electrochemical Characteristics)

oxidation potential

Bauer; Foucault; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 272; (1971); p. 192, View in Reaxys; Bordwell, F. G.; Zhao, Yongyu; Journal of Organic Chemistry; vol. 60; nb. 20; (1995); p. 6348 - 6352, View in Reaxys 4 of 15

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

acetonitrile

Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochem- -1.96 V; Product: /BRN= 6964867/. No. of transm. electrons: 1. Method: polarography. Deical Characteristics) scription: vs. Ag/0.1M AgClO4-MeCN; effects of tetraalkylammonium and alkali metal ions Product

nitromethane

Hojo, Masashi; Nishikawa, Kazukiyo; Akita, Yoshihiro; Imai, Yoshihiko; Bulletin of the Chemical Society of Japan; vol. 59; nb. 12; (1986); p. 3815 - 3820, View in Reaxys 5 of 15

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile; methanol

pH-Value (Electrochemi- 1.09 cal Characteristics)

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Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochem- -0.95 V; Product: /BRN= 1730792/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product

N-Methylhydroxylamine

Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 6 of 15

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile; methanol

pH-Value (Electrochemi- 2.1 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochem- -1.01 V; Product: /BRN= 1730792/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product

N-Methylhydroxylamine

Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 7 of 15

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile; methanol

pH-Value (Electrochemi- 3.12 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochem- -1.07 V; Product: /BRN= 1730792/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product

N-Methylhydroxylamine

Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 8 of 15

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile; methanol

pH-Value (Electrochemi- 4.05 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochem- -1.12 V; Product: /BRN= 1730792/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product

N-Methylhydroxylamine

Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys

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9 of 15

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile; methanol

pH-Value (Electrochemi- 5.08 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochem- -1.16 V; Product: /BRN= 1730792/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product

N-Methylhydroxylamine

Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 10 of 15

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile; methanol

pH-Value (Electrochemi- 6.11 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochem- -1.18 V; Product: /BRN= 1730792/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product

N-Methylhydroxylamine

Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 11 of 15

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile; methanol

pH-Value (Electrochemi- 7.12 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochem- -1.2 V; Product: /BRN= 1730792/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product

N-Methylhydroxylamine

Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 12 of 15

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile; methanol

pH-Value (Electrochemi- 8.15 cal Characteristics)

108/412

2016-04-19 03:35:30

Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochem- -1.22 V; Product: /BRN= 1730792/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product

N-Methylhydroxylamine

Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 13 of 15

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile; methanol

pH-Value (Electrochemi- 9.1 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochem- -1.23 V; Product: /BRN= 1730792/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product

N-Methylhydroxylamine

Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 14 of 15

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile; methanol

pH-Value (Electrochemi- 10.05 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochem- -1.23 V; Product: /BRN= 1730792/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product

N-Methylhydroxylamine

Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 15 of 15

Description (Electrochemical Characteristics)

polarographic current/voltage curve

Petru; Collection of Czechoslovak Chemical Communications; vol. 12; (1947); p. 621; Chem.Abstr.; (1948); p. 5354, View in Reaxys; de Vries; Ivett; Industrial and Engineering Chemistry, Analytical Edition; vol. 13; (1941); p. 339, View in Reaxys; Sifre; Memorial des Poudres; vol. 35; (1953); p. 373,380, View in Reaxys; Miquel; Condylis; Bulletin de la Societe Chimique de France; (1955); p. 236, View in Reaxys; Ballod et al.; Zhurnal Analiticheskoi Khimii; vol. 14; (1959); p. 188,191,196; engl.Ausg.S.201,204,208, View in Reaxys; Findeis; De Vries; Journal of the American Chemical Society; vol. 80; (1958); p. 797, View in Reaxys; Stewart; Bonner; Analytical Chemistry; vol. 22; (1950); p. 793, View in Reaxys; Goward et al.; Journal of Organic Chemistry; vol. 20; (1955); p. 378,384, View in Reaxys; Bergman; James; Transactions of the Faraday Society; vol. 48; (1952); p. 956,960; Transactions of the Faraday Society; vol. 50; (1954); p. 60,63, View in Reaxys Electron Binding (1) Description (Elec- References tron Binding) Electron affinity

Cumming et al.; Canadian Journal of Chemistry; vol. 55; (1977); p. 3474,3477, View in Reaxys; Compton et al.; Journal of Chemical Physics; vol. 68; (1978); p. 4360, View in Reaxys; Grimsrud, Eric P.; Caldwell, Gary; Chowdhury, Swapan; Kebarle, Paul; Journal of the American Chemical Society; vol. 107; nb. 16; (1985); p. 4627 - 4634, View in Reaxys; Chen, E. C. M.; Wentworth, W. E.; Journal of Physical Chemistry;

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vol. 87; nb. 1; (1983); p. 45 - 49, View in Reaxys; Compton; Carman Jr.; Desfrancois; Abdoul-Carmine; Schermann; Hendricks; Lyapustina; Bowen; Journal of Chemical Physics; vol. 105; nb. 9; (1996); p. 3472 - 3478, View in Reaxys Energy Barriers (3) Energy Barriers Barrier Type [Jmol-1] 48.1

Comment (Energy Barriers)

C-N

References Cataliotti, R. S.; Distefano, M. R.; Mariani, L.; Morresi, A.; Paliani, G.; et al.; Berichte der Bunsen-Gesellschaft; vol. 98; nb. 12; (1994); p. 1613 - 1618, View in Reaxys Soussen-Jacob et al.; Journal de Chimie Physique et de PhysicoChimie Biologique; vol. 67; (1970); p. 1118,1120 - 1122, 1124, View in Reaxys; Dachis et al.; Voprosy Stereokhimii; vol. 3; (1973); p. 91; Chem.Abstr.; vol. 81; nb. 151330; (1974), View in Reaxys; Zweers et al.; Physica B+C: Physics of Condensed Matter + Atomic, Molecular and Plasma Physics, Optics (Amsterdam); vol. 85; (1977); p. 239,252, View in Reaxys; Remizov; Musyakaeva; Optics and Spectroscopy; vol. 38; (1975); p. 226; ; p. 399, View in Reaxys

Potentialschwelle der inneren Rotation.

Tannenbaum et al.; Journal of Chemical Physics; vol. 25; (1956); p. 42,44, View in Reaxys

Energy Data (MCS) (128) 1 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.85

Partner (Energy Data (MCS))

benzene

Novikov; Abaidullina; Gainutdinova; Varfalomeev; Solomonov; Russian Journal of Physical Chemistry A; vol. 80; nb. 11; (2006); p. 1790 - 1794, View in Reaxys 2 of 128

Description (Energy Data (MCS))

Molar excess Gibbs free energy

Temperature (Energy Data (MCS)) [°C]

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

methanol

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 3 of 128

Description (Energy Data (MCS))

Molar excess Gibbs free energy

Temperature (Energy Data (MCS)) [°C]

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

ethanol

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 4 of 128

Description (Energy Data (MCS))

Molar excess Gibbs free energy

Temperature (Energy Data (MCS)) [°C]

Comment (Energy Data (MCS))

concentration dependence

110/412

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Partner (Energy Data (MCS))

propan-1-ol

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 5 of 128

Description (Energy Data (MCS))

Molar excess Gibbs free energy

Temperature (Energy Data (MCS)) [°C]

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

isopropyl alcohol

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 6 of 128

Description (Energy Data (MCS))

Molar excess Gibbs free energy

Temperature (Energy Data (MCS)) [°C]

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

butan-1-ol

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 7 of 128

Description (Energy Data (MCS))

Molar excess Gibbs free energy

Temperature (Energy Data (MCS)) [°C]

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

i-Butyl alcohol

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 8 of 128

Description (Energy Data (MCS))

Molar excess Gibbs free energy

Temperature (Energy Data (MCS)) [°C]

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

acetone

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 9 of 128

Description (Energy Data (MCS))

Molar excess Gibbs free energy

Temperature (Energy Data (MCS)) [°C]

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

butanone

111/412

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Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 10 of 128

Description (Energy Data (MCS))

Molar excess Gibbs free energy

Temperature (Energy Data (MCS)) [°C]

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

acetic acid methyl ester

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 11 of 128

Description (Energy Data (MCS))

Molar excess Gibbs free energy

Temperature (Energy Data (MCS)) [°C]

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

ethyl acetate

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 12 of 128

Description (Energy Data (MCS))

Molar excess Gibbs free energy

Temperature (Energy Data (MCS)) [°C]

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

tetrachloromethane

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 13 of 128

Description (Energy Data (MCS))

Molar excess Gibbs free energy

Temperature (Energy Data (MCS)) [°C]

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

benzene

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 14 of 128

Description (Energy Data (MCS))

Molar excess Gibbs free energy

Temperature (Energy Data (MCS)) [°C]

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

toluene

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys

112/412

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15 of 128

Description (Energy Data (MCS))

Enthalpy of mixing

Partner (Energy Data (MCS))

trifluoroacetic anhydride

Ivanov; Makitra; Pirig; Tsvetkov; Shmakov; Russian Journal of General Chemistry; vol. 71; nb. 10; (2001); p. 1578 - 1580, View in Reaxys 16 of 128

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

24.85

Comment (Energy Data (MCS))

concentration dependence. Object(s) of Study: diagram

Partner (Energy Data (MCS))

'Nitroglycerin'

Tsvetkov; Ivanov; Yumashev; Shipina; Marchenko; Kostochko; Russian Journal of General Chemistry; vol. 71; nb. 9; (2001); p. 1380 - 1383, View in Reaxys 17 of 128

Description (Energy Data (MCS))

Entropy of mixtures

Partner (Energy Data (MCS))

phenyltrichlorosilane and (CH3)2NSi(CH3)3 modified silica

Roshchina; Shoniya; Kitaev; Gurevich; Kaz'mina; Russian Journal of Physical Chemistry A; vol. 74; nb. 12; (2000); p. 2026 - 2033, View in Reaxys 18 of 128

Description (Energy Data (MCS))

Entropy of mixtures

Partner (Energy Data (MCS))

silica

Roshchina; Shoniya; Kitaev; Gurevich; Kaz'mina; Russian Journal of Physical Chemistry A; vol. 74; nb. 12; (2000); p. 2026 - 2033, View in Reaxys 19 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

20 - 80

Partner (Energy Data (MCS))

water

Rehak, Karel; Novak, Josef P.; Konetzna, Jana; Heintz, Andreas; Vonka, Petr; Matous, Jaroslav; Collection of Czechoslovak Chemical Communications; vol. 64; nb. 9; (1999); p. 1393 - 1411, View in Reaxys 20 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

i-Butyl alcohol

Batov; Antonova; Slyusar; Korolev; Russian Journal of General Chemistry; vol. 69; nb. 8; (1999); p. 1212 - 1218, View in Reaxys 21 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

isopropyl alcohol

Sharma; Singh, Jaibir; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 38; nb. 1; (1999); p. 65 - 69, View in Reaxys

113/412

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22 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

butan-1-ol

Sharma; Singh, Jaibir; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 38; nb. 1; (1999); p. 65 - 69, View in Reaxys 23 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Solvent (Energy Data (MCS))

H2O

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

butan-1-ol

Manin; Antonova; Korolev; Russian Journal of General Chemistry; vol. 68; nb. 2; (1998); p. 210 - 216, View in Reaxys 24 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Solvent (Energy Data (MCS))

H2O

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

iso-butanol

Manin; Antonova; Korolev; Russian Journal of General Chemistry; vol. 68; nb. 2; (1998); p. 210 - 216, View in Reaxys 25 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Solvent (Energy Data (MCS))

H2O

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

i-Butyl alcohol

Manin; Antonova; Korolev; Russian Journal of General Chemistry; vol. 68; nb. 2; (1998); p. 210 - 216, View in Reaxys 26 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Solvent (Energy Data (MCS))

H2O

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

tert-butanol

Manin; Antonova; Korolev; Russian Journal of General Chemistry; vol. 68; nb. 2; (1998); p. 210 - 216, View in Reaxys 27 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Solvent (Energy Data (MCS))

H2O

114/412

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Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

propan-1-ol

Manin; Antonova; Korolev; Russian Journal of General Chemistry; vol. 68; nb. 2; (1998); p. 210 - 216, View in Reaxys 28 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Solvent (Energy Data (MCS))

H2O

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

isopropyl alcohol

Manin; Antonova; Korolev; Russian Journal of General Chemistry; vol. 68; nb. 2; (1998); p. 210 - 216, View in Reaxys 29 of 128

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

SOCl2

Kanonerov; Tsvetkov; Lelekov; Biryukova; Russian Journal of General Chemistry; vol. 67; nb. 7; (1997); p. 1088 - 1091, View in Reaxys 30 of 128

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

SO2Cl2

Kanonerov; Tsvetkov; Lelekov; Biryukova; Russian Journal of General Chemistry; vol. 67; nb. 7; (1997); p. 1088 - 1091, View in Reaxys 31 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

acetonitrile; H2O

Vandyshev; Serebryakova; Russian Journal of General Chemistry; vol. 67; nb. 4; (1997); p. 540 - 544, View in Reaxys 32 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

DMFA; H2O

Vandyshev; Serebryakova; Russian Journal of General Chemistry; vol. 67; nb. 4; (1997); p. 540 - 544, View in Reaxys 33 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.9

115/412

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Partner (Energy Data (MCS))

tris(dimethylamino)phosphine oxide; H2O

Vandyshev; Serebryakova; Russian Journal of General Chemistry; vol. 67; nb. 4; (1997); p. 540 - 544, View in Reaxys 34 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

tert-butanol; H2O

Batov; Antonova; Svishchev; Korolev; Russian Journal of General Chemistry; vol. 66; nb. 11; (1996); p. 1727 1733, View in Reaxys 35 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

propan-1-ol

Bittrich, H.-J.; Eckert, R.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 185; nb. 2; (1994); p. 207 - 222, View in Reaxys 36 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

tetrachloromethane

Stolov, A. A.; Borisover, M. D.; Solomonov, B. N.; Kamalova, D. I.; Izosimova, S. V.; Pominov, I. S.; Russian Journal of Physical Chemistry; vol. 66; nb. 3; (1992); p. 327 - 330; Zhurnal Fizicheskoi Khimii; vol. 66; (1992); p. 620 - 625, View in Reaxys 37 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

benzene

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

acetonitrile

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

acetone

116/412

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Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

dimethyl sulfoxide

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

ethanol

Bittrich, H.-J.; Eckert, R.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 175; nb. 2; (1992); p. 217 - 234, View in Reaxys 42 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

water

Wilson, Burton; Georgiadis, Rosina; Bartmess, John E.; Journal of the American Chemical Society; vol. 113; nb. 5; (1991); p. 1762 - 1766, View in Reaxys 43 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

0.01 M aq. NaOH

Wilson, Burton; Georgiadis, Rosina; Bartmess, John E.; Journal of the American Chemical Society; vol. 113; nb. 5; (1991); p. 1762 - 1766, View in Reaxys 44 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

hexan-1-ol

Feng, Hui; Wang, Yanru; Shi, Jun; Benson, George C.; Lu, Benjamin C.-Y.; Journal of Chemical Thermodynamics; vol. 23; nb. 2; (1991); p. 169 - 174, View in Reaxys 45 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

ethylene glycol

Feng, Hui; Wang, Yanru; Shi, Jun; Benson, George C.; Lu, Benjamin C.-Y.; Journal of Chemical Thermodynamics; vol. 23; nb. 2; (1991); p. 169 - 174, View in Reaxys

117/412

2016-04-19 03:35:30

46 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

butan-1-ol

Feng, Hui; Wang, Yanru; Shi, Jun; Benson, George C.; Lu, Benjamin C.-Y.; Journal of Chemical Thermodynamics; vol. 23; nb. 2; (1991); p. 169 - 174, View in Reaxys 47 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

H2O

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 48 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

carbon disulfide

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 49 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

acetone

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 50 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

acetonitrile

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 51 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

dichloromethane

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 52 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25 - 50

Partner (Energy Data (MCS))

methanol

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys

118/412

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53 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

cyclohexane

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 54 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

tetrachloromethane

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 55 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

ethanol

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 56 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

chloroform

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 57 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

n-heptane

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 58 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

hexane

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys; Marsh, Kenneth N.; Journal of Chemical Thermodynamics; vol. 17; nb. 1; (1985); p. 29 - 42, View in Reaxys 59 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

octanol

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys

119/412

2016-04-19 03:35:30

60 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

propan-1-ol

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 61 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

butan-1-ol

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 62 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

pentane

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 63 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

2-Methylpentane

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 64 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

propiononitrile

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 65 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

propyl cyanide

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 66 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

1-Chloropropane

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 67 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

120/412

2016-04-19 03:35:30

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

n-Butyl chloride

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 68 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

Nitroethane

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 69 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

1-Nitropropane

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 70 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Partner (Energy Data (MCS))

cetane

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

18 - 30

Pressure (Energy Data (MCS)) [Torr]

759.8

Partner (Energy Data (MCS))

butan-1-ol

Battler, John R.; Rowley, Richard L.; Journal of Chemical & Engineering Data; vol. 35; nb. 3; (1990); p. 334 - 338, View in Reaxys 72 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Partner (Energy Data (MCS))

butan-1-ol

Battler, John R.; Rowley, Richard L.; Journal of Chemical & Engineering Data; vol. 35; nb. 3; (1990); p. 334 - 338, View in Reaxys 73 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

24.9 - 45.9

Partner (Energy Data (MCS))

carbon disulfide

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 35; nb. 2; (1990); p. 156 - 162, View in Reaxys 74 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

35.9 - 63.9

121/412

2016-04-19 03:35:30

Partner (Energy Data (MCS))

methanol

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 35; nb. 2; (1990); p. 156 - 162, View in Reaxys 75 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

methanol

Lee, Ikchoon; Kang, Chul Hyun; Lee, Bon-Su; Lee, Hai Whang; Journal of the Chemical Society, Faraday Transactions; vol. 86; nb. 9; (1990); p. 1477 - 1481, View in Reaxys 76 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25.1

Partner (Energy Data (MCS))

methanol

Hammerl, I.; Feinbube, A.; Herkner, K.; Bittrich, H. J.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 271; nb. 6; (1990); p. 1133 - 1138, View in Reaxys 77 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25.1

Partner (Energy Data (MCS))

ethanol

Hammerl, I.; Feinbube, A.; Herkner, K.; Bittrich, H. J.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 271; nb. 6; (1990); p. 1133 - 1138, View in Reaxys 78 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25.1

Partner (Energy Data (MCS))

propan-1-ol

Hammerl, I.; Feinbube, A.; Herkner, K.; Bittrich, H. J.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 271; nb. 6; (1990); p. 1133 - 1138, View in Reaxys 79 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25.1

Partner (Energy Data (MCS))

butan-1-ol

Hammerl, I.; Feinbube, A.; Herkner, K.; Bittrich, H. J.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 271; nb. 6; (1990); p. 1133 - 1138, View in Reaxys 80 of 128

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

tributyltin methacrylate

Konovalova, E. P.; Shmeleva, A. N.; Anisimova, S. V.; Tsvetkov, V. G.; Zabotin, K. P.; Aleksandrov, Yu. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 10.2; (1989); p. 2291 - 2293,2053 - 2055, View in Reaxys 81 of 128

Description (Energy Data (MCS))

Enthalpy of mixing

122/412

2016-04-19 03:35:30

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

hex-1-yne

Koldobskaya, L. L.; Semenov, L. V.; Gaile, A. A.; Rumyantseva, N. V.; J. Appl. Chem. USSR (Engl. Transl.); vol. 62; nb. 3.1; (1989); p. 599 - 603,551 - 555, View in Reaxys 82 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

benzene

Singh, P. P.; Dahiya, H. P.; Dagar, S.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 269; nb. 4; (1988); p. 817 - 831, View in Reaxys 83 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

toluene

Singh, P. P.; Dahiya, H. P.; Dagar, S.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 269; nb. 4; (1988); p. 817 - 831, View in Reaxys 84 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

o-xylene

Singh, P. P.; Dahiya, H. P.; Dagar, S.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 269; nb. 4; (1988); p. 817 - 831, View in Reaxys 85 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

m-xylene

Singh, P. P.; Dahiya, H. P.; Dagar, S.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 269; nb. 4; (1988); p. 817 - 831, View in Reaxys 86 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

H2O

Krestov, G. A.; Korolev, V. P.; Batov, D. V.; Doklady Chemistry; vol. 293; (1987); p. 174 - 175; Dokl. Akad. Nauk SSSR Ser. Khim.; vol. 293; nb. 4; (1987); p. 882 - 883, View in Reaxys; Korolev, V. P.; Batov, D. V.; Krestov, G. A.; Russian Journal of Physical Chemistry; vol. 59; nb. 1; (1985); p. 123 - 124; Zhurnal Fizicheskoi Khimii; vol. 59; nb. 1; (1985); p. 212 - 214, View in Reaxys 87 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Solvent (Energy Data (MCS))

H2O

123/412

2016-04-19 03:35:30

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

D2O

Krestov, G. A.; Korolev, V. P.; Batov, D. V.; Doklady Chemistry; vol. 293; (1987); p. 174 - 175; Dokl. Akad. Nauk SSSR Ser. Khim.; vol. 293; nb. 4; (1987); p. 882 - 883, View in Reaxys 88 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

D2O

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

methanol

Krestov, G. A.; Korolev, V. P.; Batov, D. V.; Doklady Chemistry; vol. 293; (1987); p. 174 - 175; Dokl. Akad. Nauk SSSR Ser. Khim.; vol. 293; nb. 4; (1987); p. 882 - 883, View in Reaxys 90 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

MeOD-d4

Krestov, G. A.; Korolev, V. P.; Batov, D. V.; Doklady Chemistry; vol. 293; (1987); p. 174 - 175; Dokl. Akad. Nauk SSSR Ser. Khim.; vol. 293; nb. 4; (1987); p. 882 - 883, View in Reaxys 91 of 128

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

deuteromethanol

Krestov, G. A.; Korolev, V. P.; Batov, D. V.; Doklady Chemistry; vol. 293; (1987); p. 174 - 175; Dokl. Akad. Nauk SSSR Ser. Khim.; vol. 293; nb. 4; (1987); p. 882 - 883, View in Reaxys 92 of 128

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

24.9

Partner (Energy Data (MCS))

tert -butyl hydrogen peroxide

Makitra, R.G.; Tsvetkov, V.G.; Pirig, Ya.N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 56; nb. 7; (1986); p. 1452 1457,1286 - 1290, View in Reaxys 93 of 128

Description (Energy Data (MCS))

Enthalpy of mixtures

Partner (Energy Data (MCS))

n-propyl-nonadecane

124/412

2016-04-19 03:35:30

Kozin, V. G.; Diyarov, I. N.; Almazova, G. A.; Masenkov, V. S.; Russian Journal of Physical Chemistry; vol. 60; nb. 8; (1986); p. 1124 - 1126; Zhurnal Fizicheskoi Khimii; vol. 60; (1986); p. 1868 - 1871, View in Reaxys 94 of 128

Description (Energy Data (MCS))

Enthalpy of mixtures

Partner (Energy Data (MCS))

palmityl alcohol

Description (Energy Data (MCS))

Enthalpy of mixtures

Partner (Energy Data (MCS))

1-hexadecylcarboxylic acid

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

298

Partner (Energy Data (MCS))

HNO3

Tsvetkov, V. G.; Marchenko, G. N.; Sopin, V. F.; Tsverkova, L. Ya.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 2; (1985); p. 233 - 238,201 - 205, View in Reaxys 97 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25 - 45

Partner (Energy Data (MCS))

cyclohexane

Marsh, Kenneth N.; Journal of Chemical Thermodynamics; vol. 17; nb. 1; (1985); p. 29 - 42, View in Reaxys 98 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

2,3-dimethyl-butane

Marsh, Kenneth N.; Journal of Chemical Thermodynamics; vol. 17; nb. 1; (1985); p. 29 - 42, View in Reaxys 99 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25 - 45

Partner (Energy Data (MCS))

tetrachloromethane

Marsh, Kenneth N.; Journal of Chemical Thermodynamics; vol. 17; nb. 1; (1985); p. 29 - 42, View in Reaxys 100 of 128 Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

para-xylene

Marsh, Kenneth N.; Journal of Chemical Thermodynamics; vol. 17; nb. 1; (1985); p. 29 - 42, View in Reaxys 101 of 128 Description (Energy Data (MCS))

Excess thermochemical parameter

125/412

2016-04-19 03:35:30

Temperature (Energy Data (MCS)) [°C]

25 - 45

Partner (Energy Data (MCS))

benzene

Marsh, Kenneth N.; Journal of Chemical Thermodynamics; vol. 17; nb. 1; (1985); p. 29 - 42, View in Reaxys 102 of 128 Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

petroleum sulfoxides

Kozin; Diyarov; Komleva; Antoshkova; Journal of applied chemistry of the USSR; vol. 57; nb. 5 pt 2; (1984); p. 1007 - 1010, View in Reaxys 103 of 128 Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

butyl sulfoxide

Kozin; Diyarov; Komleva; Antoshkova; Journal of applied chemistry of the USSR; vol. 57; nb. 5 pt 2; (1984); p. 1007 - 1010, View in Reaxys 104 of 128 Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

diphenyl sulphoxide

Kozin; Diyarov; Komleva; Antoshkova; Journal of applied chemistry of the USSR; vol. 57; nb. 5 pt 2; (1984); p. 1007 - 1010, View in Reaxys 105 of 128 Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

petroleum sulfones

Kozin; Diyarov; Komleva; Antoshkova; Journal of applied chemistry of the USSR; vol. 57; nb. 5 pt 2; (1984); p. 1007 - 1010, View in Reaxys 106 of 128 Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

2,4-dimethyl sulfolane

Kozin; Diyarov; Komleva; Antoshkova; Journal of applied chemistry of the USSR; vol. 57; nb. 5 pt 2; (1984); p. 1007 - 1010, View in Reaxys 107 of 128 Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

petroleum sulfides

Kozin; Diyarov; Komleva; Antoshkova; Journal of applied chemistry of the USSR; vol. 57; nb. 5 pt 2; (1984); p. 1007 - 1010, View in Reaxys

126/412

2016-04-19 03:35:30

108 of 128 Description (Energy Data (MCS)) Partner (Energy Data (MCS))

Enthalpy of mixing ethylenediamine

Makitra, R. G.; Pirig, Ya. N.; Tsvetkov, V. G.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 4; (1984); p. 833 836,740 - 742, View in Reaxys 109 of 128 Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

chloroform

Kiselev, V. D.; Veisman, E. A.; Zabotina, O. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 53; nb. 2; (1983); p. 333 342,289 - 297, View in Reaxys 110 of 128

Description (Energy Data (MCS))

Enthalpy of mixing

Partner (Energy Data (MCS))

bromine

Makitra, R. G.; Pirig, Ya. N.; Tsvetkov, V. G.; J. Gen. Chem. USSR (Engl. Transl.); vol. 53; nb. 4; (1983); p. 727 732,633 - 638, View in Reaxys 111 of 128

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

46.9

Partner (Energy Data (MCS))

phenol

Tsvetkov, V. G.; Perov, V. A.; Gatilov, Yu. F.; Aleksandrov, Yu. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 51; nb. 6; (1981); p. 1376 - 1379,1166 - 1168, View in Reaxys 112 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

30 - 40

Partner (Energy Data (MCS))

benzene

Nigam, Ram K.; Singh, Prem P.; Mishra, Ruchi; Singh, Mohan; Canadian Journal of Chemistry; vol. 58; (1980); p. 1468 - 1472, View in Reaxys 113 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

30 - 40

Partner (Energy Data (MCS))

toluene

Nigam, Ram K.; Singh, Prem P.; Mishra, Ruchi; Singh, Mohan; Canadian Journal of Chemistry; vol. 58; (1980); p. 1468 - 1472, View in Reaxys 114 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

30 - 40

Partner (Energy Data (MCS))

o-xylene

Nigam, Ram K.; Singh, Prem P.; Mishra, Ruchi; Singh, Mohan; Canadian Journal of Chemistry; vol. 58; (1980); p. 1468 - 1472, View in Reaxys

127/412

2016-04-19 03:35:30

115 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

30 - 40

Partner (Energy Data (MCS))

m-xylene

Nigam, Ram K.; Singh, Prem P.; Mishra, Ruchi; Singh, Mohan; Canadian Journal of Chemistry; vol. 58; (1980); p. 1468 - 1472, View in Reaxys 116 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

30 - 40

Partner (Energy Data (MCS))

para-xylene

Nigam, Ram K.; Singh, Prem P.; Mishra, Ruchi; Singh, Mohan; Canadian Journal of Chemistry; vol. 58; (1980); p. 1468 - 1472, View in Reaxys 117 of 128

Description (Energy Data (MCS))

Enthalpy of mixing

Tsvetkov et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 48; (1978); p. 2162,1966, View in Reaxys; Tsvetkov et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 49; (1979); p. 485,426, View in Reaxys; Tsvetkov et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 47; (1977); p. 729,665, View in Reaxys; Chaldna; Pjuss; Russian Journal of Physical Chemistry; vol. 38; (1964); p. 1519; Zhurnal Fizicheskoi Khimii; vol. 38; (1964); p. 2807, View in Reaxys; Becker et al.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 39; (1963); p. 306,314,318, View in Reaxys; Becker et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 23; (1968); p. 1805,1813, View in Reaxys; Addison et al.; Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999); (1974); p. 999,1000, View in Reaxys 118 of 128

Description (Energy Data (MCS))

Excess thermochemical parameter

Marsh et al.; Journal of Chemical Thermodynamics; vol. 11; (1979); p. 897,899 - 901, View in Reaxys; Clever; Hsu; Journal of Chemical Thermodynamics; vol. 10; (1978); p. 213,214, 216 - 218, View in Reaxys; Nigam et al.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 18; (1979); p. 492, View in Reaxys; Derrick; Clever; Journal of Physical Chemistry; vol. 75; (1971); p. 3728, View in Reaxys 119 of 128

Description (Energy Data (MCS))

Thermodynamic properties of system with

Benoit; Milanova; Canadian Journal of Chemistry; vol. 57; (1979); p. 1319,1321, View in Reaxys; Cox; Parker; Journal of the American Chemical Society; vol. 95; (1973); p. 402,403-407, View in Reaxys; Suri et al.; Indian Journal of Chemistry; vol. 12; (1974); p. 620, View in Reaxys; Kaulgud; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 36; (1963); p. 365,372, 373, View in Reaxys; Abraham; Grellier; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1975); p. 1856, View in Reaxys; Iogansen; Theoretical and Experimental Chemistry; vol. 7; (1971); p. 249,253; ; p. 302, View in Reaxys; Aleksandrov; Chernyi; Russian Journal of Physical Chemistry; vol. 50; (1976); p. 299; ; p. 516, View in Reaxys; Clever et al.; Journal of Chemical and Engineering Data; vol. 17; (1972); p. 31,33, View in Reaxys 120 of 128 Description (Energy Data (MCS))

Enthalpy of solution

Cox,B.G.; Parker,A.J.; Journal of the American Chemical Society; vol. 95; (1973); p. 408 - 410, View in Reaxys; Cox; Parker; Journal of the American Chemical Society; vol. 95; (1973); p. 402,403-407, View in Reaxys; Cox et al.; Journal of the American Chemical Society; vol. 95; (1973); p. 1010, View in Reaxys; Evered; Pollard; Journal of Chromatography; vol. 4; (1960); p. 451,452-457; Chem.Abstr.; nb. 14011; (1961), View in Reaxys; Stern; Hermann; Journal of Physical Chemistry; vol. 71; (1967); p. 309,311, View in Reaxys; Stern; Swearingen; Journal of Physical Chemistry; vol. 74; (1970); p. 167, View in Reaxys; Gukalova; Korol'; Russian Journal of Physical Chemistry; vol. 44; (1970); p. 652; ; p. 1171, View in Reaxys 121 of 128 Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

acetone

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Brown; Fock; Australian Journal of Chemistry; vol. 10; (1957); p. 417,419, View in Reaxys 122 of 128 Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

tetrachloromethane

Brown; Fock; Australian Journal of Chemistry; vol. 9; (1956); p. 180, View in Reaxys 123 of 128 Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

benzene

Brown; Fock; Australian Journal of Chemistry; vol. 9; (1956); p. 180, View in Reaxys 124 of 128 Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

acetonitrile

Brown; Fock; Australian Journal of Chemistry; vol. 9; (1956); p. 180, View in Reaxys 125 of 128 Description (Energy Data (MCS)) Partner (Energy Data (MCS))

Enthalpy of mixing Benzyl acetate

Moore; Styan; Transactions of the Faraday Society; vol. 52; (1956); p. 1556,1559, View in Reaxys 126 of 128 Description (Energy Data (MCS)) Partner (Energy Data (MCS))

Enthalpy of mixing Glutaronitrile

Phibbs; Journal of Physical Chemistry; vol. 59; (1935); p. 346,349, View in Reaxys 127 of 128 Description (Energy Data (MCS))

Enthalpy of mixing

Comment (Energy Data (MCS))

Loesungswaerme.

Partner (Energy Data (MCS))

(C2H5)4Ni

Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 58; (1907); p. 489, View in Reaxys 128 of 128 Description (Energy Data (MCS))

Enthalpy of mixing

Comment (Energy Data (MCS))

Loesungswaerme.

Partner (Energy Data (MCS))

(C3H7)4Ni

Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 58; (1907); p. 489, View in Reaxys Enthalpies of Other Phase Transitions (1) Enthalpies of Oth- Comment (EnReferences er Phase Transi- thalpies of Other tions [Jmol-1]

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Phase Transitions) -7100

From transfer Goffredi, Mario; Liszi, Janos; Nemeth, Bela; Liveri, Vincenzo Turco; Journal of Solufrom n-octane to tion Chemistry; vol. 12; nb. 4; (1983); p. 221 - 232, View in Reaxys water at 25 deg to C

Enthalpy of Combustion (4) Enthalpy of Com- Comment (Enbustion [Jmol-1] thalpy of Combustion)

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in fluess. Zustand.

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-757387

in Dampf.

Thomsen; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 52; (1905); p. 343; Thermochemische Untersuchungen; vol. 4; p. 104, View in Reaxys

-710914

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Berthelot; Matignon; Annales de Chimie (Cachan, France); vol. <6> 30; (1893); p. 557, View in Reaxys

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Enthalpy of Vaporization (9) Enthalpy of VaTemperature (Enporization thalpy of Vapori[Jmol-1] zation) [°C]

Comment (Enthalpy of Vaporization)

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38518.6

24.85

Miroshnichenko; Vorob'eva; Russian Journal of Physical Chemistry A; vol. 73; nb. 3; (1999); p. 349 - 355, View in Reaxys

36215.8

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Langlet, J.; Claverie, P.; Caillet, J.; Pullman, A.; Journal of Physical Chemistry; vol. 92; nb. 6; (1988); p. 1617 - 1631, View in Reaxys

37597.4

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Langlet, J.; Claverie, P.; Caillet, J.; Pullman, A.; Journal of Physical Chemistry; vol. 92; nb. 6; (1988); p. 1617 - 1631, View in Reaxys

38400

Kiselev, V. D.; Veisman, E. A.; Zabotina, O. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 53; nb. 2; (1983); p. 333 - 342,289 - 297, View in Reaxys

33996.8

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37191.3

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38296.7

Jones; Giauque; Journal of the American Chemical Society; vol. 69; (1947); p. 984, View in Reaxys enthalpy of vapor- Pitzer; Gwinn; Journal of the American Chemical Society; vol. 63; ization:8225+-25 (1941); p. 3313, View in Reaxys Joule/Mol.

34485.6

99.9

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Further Information (162)

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Description (Further Information)

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Komarowa; Kogan; J. Appl. Chem. USSR (Engl. Transl.); vol. 37; (1964); p. 1776,1764, View in Reaxys

Further information

Chaldna et al.; Russian Journal of Physical Chemistry; vol. 38; (1964); p. 469; Zhurnal Fizicheskoi Khimii; vol. 38; (1964); p. 863, View in Reaxys

Further information

Dremin; Rosanow; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1964); p. 1417; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1964); p. 1513, View in Reaxys

Further information

Herbison-Evans; Richards; Molecular Physics; vol. 8; (1964); p. 19,26, View in Reaxys

Further information

Feuer,H. et al.; Spectrochimica Acta; vol. 19; (1963); p. 431 - 434, View in Reaxys

Further information

Woronkow; Deitsch; Journal fuer Praktische Chemie (Leipzig); vol. 22; (1963); p. 214,221, View in Reaxys

Further information

Padmini et al.; Journal of the Physical Society of Japan; vol. 18; (1963); p. 871,874, View in Reaxys

Further information

Dullien; Transactions of the Faraday Society; vol. 59; (1963); p. 856,862, View in Reaxys

Further information

Hammond; Journal of the Chemical Society; (1963); p. 2565, View in Reaxys

Further information

Schwetlick et al.; Journal fuer Praktische Chemie (Leipzig); vol. 22; (1963); p. 113,119, View in Reaxys

Further information

Lieser; Guetlich; Berichte der Bunsen-Gesellschaft; vol. 67; (1963); p. 445, View in Reaxys

Further information

Yarwood; Orville-Thomas; Journal of the Chemical Society; (1963); p. 5991, View in Reaxys

Further information

Kazmirowski; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 3; (1963); p. 228, View in Reaxys

Further information

Gal'perin; Shvedov; Russian Journal of Physical Chemistry; vol. 37; (1963); p. 631; ; p. 1182, View in Reaxys

Further information

Popov; Shlyapochnikov; Optics and Spectroscopy; vol. 14; (1963); p. 413; ; p. 779, View in Reaxys

Further information

Martin; Yay; Analytical Chemistry; vol. 34; (1962); p. 1007, View in Reaxys

Further information

Watanabe et al.; Journal of Quantitative Spectroscopy and Radiative Transfer; vol. 2; (1962); p. 369,377, View in Reaxys

Further information

Francois; Bulletin de la Societe Chimique de France; (1962); p. 511, View in Reaxys

Further information

Englert; Zeitschrift fuer Elektrochemie; vol. 65; (1961); p. 854, View in Reaxys

Further information

Jonathan; Journal of Molecular Spectroscopy; vol. 7; (1961); p. 105,108, View in Reaxys

Further information

Decroocq; Jungers; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 252; (1961); p. 1454,1455, View in Reaxys

Further information

Jones; Sheppard; Proceedings of the Chemical Society, London; (1961); p. 420, View in Reaxys

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Further information

Urbanski; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 9; (1961); p. 321, View in Reaxys

Further information

Sumarokowa; Litwiak; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 352,316; Chem.Abstr.; nb. 24365; (1961), View in Reaxys

Further information

Swain; Thornton; Tetrahedron Letters; (1961); p. 211, View in Reaxys

Further information

Ilyukhin et al.; Sov. Phys. Dokl. (Engl. Transl.); vol. 5; (1960); p. 793,337, View in Reaxys

Further information

de Maine et al.; Canadian Journal of Chemistry; vol. 38; (1960); p. 1921,1923, View in Reaxys

Further information

Balasubramanian; Rao; Chemistry and Industry (London, United Kingdom); (1960); p. 1025, View in Reaxys

Further information

McEwen; Journal of Chemical Physics; vol. 32; (1960); p. 1801,1806, View in Reaxys

Further information

Patent; Boschan, Smith, U.S. Dep. Comm. Off. Tech. Serv. Rep.; US151120; (1957); Chem.Abstr.; nb. 10497; (1960), View in Reaxys

Heat Capacity Cp (7) Heat Capacity Cp Temperature [Jmol-1K-1] (Heat Capacity Cp) [°C] 105

Comment (Heat Capacity Cp)

-3.1

References

Dvorkin, P. L.; Ryzhova, G. L.; Lebedev, Yu. A.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 33; (1984); p. 982 - 987; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 5; (1984); p. 1069 1074, View in Reaxys Reese et al.; Journal of Chemical and Engineering Data; vol. 15; (1970); p. 140,141, View in Reaxys; Stern; Swearingen; Journal of Physical Chemistry; vol. 74; (1970); p. 167, View in Reaxys des Dampfes bei 0.25-1 atm und 90 - 250grad.

McCullough et al.; Journal of the American Chemical Society; vol. 76; (1954); p. 4791,4793,4794, View in Reaxys

107.85 - 114.49

30 - 100

Hough et al.; Journal of the American Chemical Society; vol. 72; (1950); p. 5775, View in Reaxys

2.92 - 105.84

-259.9 - 24

Jones; Giauque; Journal of the American Chemical Society; vol. 69; (1947); p. 984, View in Reaxys

15 - 65

Williams; Journal of the American Chemical Society; vol. 47; (1925); p. 2646, View in Reaxys

Heat Capacity Cv (1) References Cowperthwaite; Shaw; Journal of Chemical Physics; vol. 53; (1970); p. 555,558, View in Reaxys; Reese et al.; Journal of Chemical and Engineering Data; vol. 15; (1970); p. 140,141, View in Reaxys Interatomic Distances and Angles (2) Description References Interatomic distances and angles

Mezey et al.; Canadian Journal of Chemistry; vol. 54; (1976); p. 2526, View in Reaxys; Melander; Bergmann; Acta Chemica Scandinavica, Series A: Physical and Inorganic Chemistry; vol. 30; (1976); p. 703, View in Reaxys; Bagryanskaya, Yu. i.; Gatilov, Yu. V.; Journal of Structural Chemistry; vol. 24; nb. 1; (1983); p. 150 - 151; Zhurnal Strukturnoi Khimii; vol. 24; nb. 1; (1983); p. 158 - 160, View in Reaxys; Trevino, S. F.; Prince, E.; Hubbard, C. R.; Journal of Chemical Physics; vol. 73; nb. 6; (1980); p. 2996 - 3000, View in Reaxys

Electron distribution

Kruppa; Suhr; Janzen; Staib; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 85; nb. 12; (1981); p. 1128 - 1132, View in Reaxys

Ionization Potential (1) References Kandel; Journal of Chemical Physics; vol. 23; (1955); p. 84,85, View in Reaxys; Collin; Bulletin de la Societe Royale des Sciences de Liege; vol. 23; (1954); p. 194 - 196, View in Reaxys; Gibson; Canadian Journal of Chemistry; vol. 55; (1977); p.

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2637,2638, View in Reaxys; Gropen; Skancke; Acta Chemica Scandinavica (1947-1973); vol. 24; (1970); p. 1768, View in Reaxys; Lipei; Potapov; High Energy Chemistry; vol. 9; (1975); p. 290; ; p. 332, View in Reaxys; Watanabe et al.; Journal of Quantitative Spectroscopy and Radiative Transfer; vol. 2; (1962); p. 369,377, View in Reaxys; Nicholson; Journal of Chemical Physics; vol. 43; (1965); p. 1171,1173, View in Reaxys; Rabalais; Journal of Chemical Physics; vol. 57; (1972); p. 960, View in Reaxys; Kobayashi; Nagakura; Bulletin of the Chemical Society of Japan; vol. 47; (1974); p. 2563, View in Reaxys; Malarski; Roczniki Chemii; vol. 48; (1974); p. 663,666, View in Reaxys Kinematic Viscosity (3) Kinematic Viscos- Temperature (Kin- References ity [St] ematic Viscosity) [°C] 0.00489 0.00601

20 - 35

Makowska, Anna; Szydlowski, Jerzy; Journal of Chemical and Engineering Data; vol. 50; nb. 4; (2005); p. 1365 - 1369, View in Reaxys

0.00557

25.31 - 28.91

283.2 - 298.2

Liquid Phase (4) Description (Liquid Phase)

Comment (Liquid Phase)

References

Self-association in solution

Burmistrov, V. A.; Aleksandriiskii, V. V.; Russian Journal of Physical Chemistry; vol. 64; nb. 3; (1990); p. 439 - 441; Zhurnal Fizicheskoi Khimii; vol. 64; (1990); p. 826 - 829, View in Reaxys; Cataliotti, R. S.; Paliani, G.; Mariani, L.; Santini, S.; Giorgini, M. G.; Journal of Physical Chemistry; vol. 96; nb. 7; (1992); p. 2961 - 2964, View in Reaxys; AlShawabkeh, Ali F.; Al-Wahab, Haitham A.; Shahab, Yousif A.; Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy; vol. 66; nb. 3; (2007); p. 739 - 744, View in Reaxys

Structure of the liquid

Greffe; Barriol; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 69; (1972); p. 1579,1584, 1585, View in Reaxys; Burmistrov, V. A.; Aleksandriiskii, V. V.; Russian Journal of Physical Chemistry; vol. 64; nb. 3; (1990); p. 439 - 441; Zhurnal Fizicheskoi Khimii; vol. 64; (1990); p. 826 - 829, View in Reaxys; Demidov; Libov; Russian Journal of Physical Chemistry A; vol. 71; nb. 12; (1997); p. 1997 - 1999, View in Reaxys

Association in the liquid state

Skomorokhov, V. I.; Dregalin, A. F.; Russian Journal of Physical Chemistry; vol. 66; nb. 11; (1992); p. 1569 - 1572; Zhurnal Fizicheskoi Khimii; vol. 66; (1992); p. 2947 - 2953, View in Reaxys; Demidov; Libov; Russian Journal of Physical Chemistry A; vol. 71; nb. 12; (1997); p. 1997 - 1999, View in Reaxys

Self-association in solution

in TetrachlormeDe Maine et al.; Transactions of the Faraday Society; vol. 53; (1957); p. 427,428, than und in Cyclo- View in Reaxys hexan.

Liquid/Liquid Systems (MCS) (108) 1 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Partner (Liquid/Liquid Systems (MCS))

ethylene glycol

Milewska; Siporska; Szydlowski; Polish Journal of Chemistry; vol. 78; nb. 4; (2004); p. 591 - 594, View in Reaxys 2 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

29.5 - 30

Partner (Liquid/Liquid Systems (MCS))

hexan-1-ol; 1-octanoic acid

Sazonov, Valerii P.; Lisov, Nikolai I.; Sazonov, Nikolai V.; Journal of Chemical and Engineering Data; vol. 47; nb. 3; (2002); p. 599 - 602, View in Reaxys 3 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

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Temperature (Liquid/ Liquid Systems (MCS)) [°C]

29.5 - 30

Partner (Liquid/Liquid Systems (MCS))

hexan-1-ol; 1-octanoic acid

Sazonov, Valerii P.; Lisov, Nikolai I.; Sazonov, Nikolai V.; Journal of Chemical and Engineering Data; vol. 47; nb. 3; (2002); p. 599 - 602, View in Reaxys 4 of 108

Description (Liquid/ Liquid Systems (MCS))

Solubility diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

17.3 - 35.6

Partner (Liquid/Liquid Systems (MCS))

hexan-1-ol

Sazonov, Valerii P.; Lisov, Nikolai I.; Sazonov, Nikolai V.; Journal of Chemical and Engineering Data; vol. 47; nb. 3; (2002); p. 599 - 602, View in Reaxys 5 of 108

Description (Liquid/ Liquid Systems (MCS))

Solubility diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

16.5 - 35

Partner (Liquid/Liquid Systems (MCS))

1-octanoic acid

Sazonov, Valerii P.; Lisov, Nikolai I.; Sazonov, Nikolai V.; Journal of Chemical and Engineering Data; vol. 47; nb. 3; (2002); p. 599 - 602, View in Reaxys 6 of 108

Description (Liquid/ Liquid Systems (MCS))

Solubility diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

20 - 35

Partner (Liquid/Liquid Systems (MCS))

hexan-1-ol; 1-octanoic acid

Sazonov, Valerii P.; Lisov, Nikolai I.; Sazonov, Nikolai V.; Journal of Chemical and Engineering Data; vol. 47; nb. 3; (2002); p. 599 - 602, View in Reaxys 7 of 108

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Partner (Liquid/Liquid Systems (MCS))

n-heptane; ethylene glycol

Abraham, Michael H.; Martins, Filomena; Mitchell, Robert C.; Salter, Colin J.; Journal of Pharmaceutical Sciences; vol. 88; nb. 2; (1999); p. 241 - 247, View in Reaxys 8 of 108

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Comment (Liquid/Liquid Systems (MCS))

equation

Partner (Liquid/Liquid Systems (MCS))

chloroform

Abraham, Michael H.; Platts, James A.; Hersey, Anne; Leo, Albert J.; Taft, Robert W.; Journal of Pharmaceutical Sciences; vol. 88; nb. 7; (1999); p. 670 - 679, View in Reaxys 9 of 108

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Comment (Liquid/Liquid Systems (MCS))

equation

Partner (Liquid/Liquid Systems (MCS))

chloroform

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Abraham, Michael H.; Platts, James A.; Hersey, Anne; Leo, Albert J.; Taft, Robert W.; Journal of Pharmaceutical Sciences; vol. 88; nb. 7; (1999); p. 670 - 679, View in Reaxys 10 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

23.85 - 29.85

Partner (Liquid/Liquid Systems (MCS))

n-pentan-1-ol

Szydlowski; Milewska; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 505 - 508, View in Reaxys 11 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

23.85 - 29.85

Partner (Liquid/Liquid Systems (MCS))

1-pentanol-d1

Szydlowski; Milewska; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 505 - 508, View in Reaxys 12 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

23.85 - 29.85

Partner (Liquid/Liquid Systems (MCS))

i-Butyl alcohol

Szydlowski; Milewska; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 505 - 508, View in Reaxys 13 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

23.85 - 29.85

Partner (Liquid/Liquid Systems (MCS))

iso-BuOD

Szydlowski; Milewska; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 505 - 508, View in Reaxys 14 of 108

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

gas

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

39.2

Partner (Liquid/Liquid Systems (MCS))

apolane

Weckwerth, Jeff D.; Carr, Peter W.; Vitha, Mark F.; Nasehzadeh, Asad; Analytical Chemistry; vol. 70; nb. 17; (1998); p. 3712 - 3716, View in Reaxys 15 of 108

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.85

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Partner (Liquid/Liquid Systems (MCS))

cetane; methanol

Abraham, Michael H.; Whiting, Gary S.; Carr, Peter W.; Ouyang, Hsiu; Journal of the Chemical Society. Perkin Transactions 2; nb. 6; (1998); p. 1385 - 1390, View in Reaxys 16 of 108

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Partner (Liquid/Liquid Systems (MCS))

dibutyl ether; H2O

Pagliara, Alessandra; Caron, Giulia; Lisa, Giuseppe; Fan, Weizheng; Gaillard, Patrick; Carrupt, Pierre-Alain; Testa, Bernard; Abraham, Michael H.; Journal of the Chemical Society. Perkin Transactions 2; nb. 12; (1997); p. 2639 - 2643, View in Reaxys 17 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

33 - 50

Partner (Liquid/Liquid Systems (MCS))

2,2'-iminobis[ethanol]; 1-Octanol

Zhuravleva, I. K.; Gabbasov, T. M.; Russian Journal of Physical Chemistry; vol. 69; nb. 9; (1995); p. 1554 - 1555; Zhurnal Fizicheskoi Khimii; vol. 69; nb. 9; (1995); p. 1711 - 1712, View in Reaxys 18 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

33 - 50

Partner (Liquid/Liquid Systems (MCS))

1-Octanol; 2,2'-iminobis[ethanol]

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

15 - 43

Partner (Liquid/Liquid Systems (MCS))

1-undecanol; ethylene glycol

Zhuravleva, I. K.; Galieva, E. R.; Russian Journal of General Chemistry; vol. 64; nb. 7.1; (1994); p. 988 - 992; Zhurnal Obshchei Khimii; vol. 64; nb. 7; (1994); p. 1096 - 1100, View in Reaxys 20 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

3 - 85

Partner (Liquid/Liquid Systems (MCS))

1-undecanol; ethylene glycol

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Partner (Liquid/Liquid Systems (MCS))

2,2'-iminobis[ethanol]; 1-heptanol

Zhuravleva, I. K.; Gabbasov, T. M.; Russian Journal of General Chemistry; vol. 64; nb. 12.1; (1994); p. 1730 1732; Zhurnal Obshchei Khimii; vol. 64; nb. 12; (1994); p. 1948 - 1950, View in Reaxys

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22 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

ethylene glycol; water

Kubicek, Vladimir; Novak, Josef P.; Matous, Jaroslav; Collection of Czechoslovak Chemical Communications; vol. 58; nb. 5; (1993); p. 983 - 995, View in Reaxys 23 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Partner (Liquid/Liquid Systems (MCS))

ethylene glycol; water

Kubicek, Vladimir; Novak, Josef P.; Matous, Jaroslav; Collection of Czechoslovak Chemical Communications; vol. 58; nb. 5; (1993); p. 983 - 995, View in Reaxys 24 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Partner (Liquid/Liquid Systems (MCS))

tert-butyl methyl ether; water

Kubicek, Vladimir; Novak, Josef P.; Matous, Jaroslav; Collection of Czechoslovak Chemical Communications; vol. 58; nb. 5; (1993); p. 983 - 995, View in Reaxys 25 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

tert-butyl methyl ether; water

Kubicek, Vladimir; Novak, Josef P.; Matous, Jaroslav; Collection of Czechoslovak Chemical Communications; vol. 58; nb. 5; (1993); p. 983 - 995, View in Reaxys 26 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

tert-butyl methyl ether; ethylene glycol; water

Kubicek, Vladimir; Novak, Josef P.; Matous, Jaroslav; Collection of Czechoslovak Chemical Communications; vol. 58; nb. 5; (1993); p. 983 - 995, View in Reaxys 27 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

tert-butyl methyl ether; ethylene glycol

Kubicek, Vladimir; Novak, Josef P.; Matous, Jaroslav; Collection of Czechoslovak Chemical Communications; vol. 58; nb. 5; (1993); p. 983 - 995, View in Reaxys 28 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Partner (Liquid/Liquid Systems (MCS))

tert-butyl methyl ether; ethylene glycol

Kubicek, Vladimir; Novak, Josef P.; Matous, Jaroslav; Collection of Czechoslovak Chemical Communications; vol. 58; nb. 5; (1993); p. 983 - 995, View in Reaxys

142/412

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29 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

H2O, EtOH

Rezanova, E. N.; Toikka, A. M.; Markuzin, N. P.; Russian Journal of Applied Chemistry; vol. 66; nb. 2.2; (1993); p. 293 - 296; Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation); vol. 66; nb. 2; (1993); p. 359 - 363, View in Reaxys 30 of 108

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Partner (Liquid/Liquid Systems (MCS))

cetane; water

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Pressure (Liquid/Liquid Systems (MCS)) [Torr]

759.8

Partner (Liquid/Liquid Systems (MCS))

butan-1-ol

Battler, John R.; Rowley, Richard L.; Journal of Chemical & Engineering Data; vol. 35; nb. 3; (1990); p. 334 - 338, View in Reaxys 32 of 108

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Partner (Liquid/Liquid Systems (MCS))

n-heptane

Sazonov, V. P.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 11.1; (1989); p. 2431 - 2435,2173 - 2176, View in Reaxys 33 of 108

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Partner (Liquid/Liquid Systems (MCS))

1-heptanol

Sazonov, V. P.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 11.1; (1989); p. 2431 - 2435,2173 - 2176, View in Reaxys 34 of 108

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Partner (Liquid/Liquid Systems (MCS))

1-Decanol

Sazonov, V. P.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 11.1; (1989); p. 2431 - 2435,2173 - 2176, View in Reaxys 35 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

34.9 - 74.9

Partner (Liquid/Liquid Systems (MCS))

ethylene glycol; 1,1,2,2-tetrachloroethylene; n-heptane

Sazonov, V. P.; Chernysheva, M. F.; J. Gen. Chem. USSR (Engl. Transl.); vol. 57; nb. 1; (1987); p. 46 - 54,38 - 44, View in Reaxys

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36 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Partner (Liquid/Liquid Systems (MCS))

n-heptane; 1,1,2,2-tetrachloroethylene; ethylene glycol

Sazonov, V. P.; Chernysheva, M. F.; J. Gen. Chem. USSR (Engl. Transl.); vol. 57; nb. 1; (1987); p. 46 - 54,38 - 44, View in Reaxys 37 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

46.9 - 76.9

Partner (Liquid/Liquid Systems (MCS))

n-heptane; 1,1,2,2-tetrachloroethylene; ethylene glycol

Sazonov, V. P.; Chernysheva, M. F.; J. Gen. Chem. USSR (Engl. Transl.); vol. 57; nb. 1; (1987); p. 46 - 54,38 - 44, View in Reaxys 38 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

34.9 - 74.9

Partner (Liquid/Liquid Systems (MCS))

n-heptane; 1,1,2,2-tetrachloroethylene; ethylene glycol

Sazonov, V. P.; Chernysheva, M. F.; J. Gen. Chem. USSR (Engl. Transl.); vol. 57; nb. 1; (1987); p. 46 - 54,38 - 44, View in Reaxys 39 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

20 - 56.6

Partner (Liquid/Liquid Systems (MCS))

ethylene glycol; 1,1,2,2-tetrachloroethylene

Sazonov, V. P.; J. Appl. Chem. USSR (Engl. Transl.); vol. 59; nb. 1; (1986); p. 12 - 18,10 - 15, View in Reaxys 40 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

20 - 56.6

Partner (Liquid/Liquid Systems (MCS))

ethylene glycol; 1,1,2,2-tetrachloroethylene

Sazonov, V. P.; J. Appl. Chem. USSR (Engl. Transl.); vol. 59; nb. 1; (1986); p. 12 - 18,10 - 15, View in Reaxys 41 of 108

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

56.6

Partner (Liquid/Liquid Systems (MCS))

ethylene glycol; 1,1,2,2-tetrachloroethylene

Sazonov, V. P.; J. Appl. Chem. USSR (Engl. Transl.); vol. 59; nb. 1; (1986); p. 12 - 18,10 - 15, View in Reaxys 42 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

40 - 56.6

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Partner (Liquid/Liquid Systems (MCS))

1,1,2,2-tetrachloroethylene; ethylene glycol

Sazonov, V. P.; Chernysheva, M. F.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 11; (1985); p. 2440 2446,2167 - 2172, View in Reaxys 43 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

40 - 56.6

Partner (Liquid/Liquid Systems (MCS))

ethylene glycol; 1,1,2,2-tetrachloroethylene

Sazonov, V. P.; Chernysheva, M. F.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 11; (1985); p. 2440 2446,2167 - 2172, View in Reaxys 44 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

0 - 50

Partner (Liquid/Liquid Systems (MCS))

1-heptanol; ethylene glycol

Zhuravleva, I. K.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 8; (1985); p. 1685 - 1689,1496 - 1500, View in Reaxys 45 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

0 - 50

Partner (Liquid/Liquid Systems (MCS))

1-Octanol; ethylene glycol

Zhuravleva, I. K.; J. Gen. Chem. USSR (Engl. Transl.); vol. 55; nb. 8; (1985); p. 1685 - 1689,1496 - 1500, View in Reaxys 46 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Partner (Liquid/Liquid Systems (MCS))

2,2'-iminobis[ethanol]; 1-undecanol

Zhuravleva, I. K.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 5; (1984); p. 982 - 985,874 - 876, View in Reaxys 47 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Partner (Liquid/Liquid Systems (MCS))

2,2'-iminobis[ethanol]; 1-Decanol

Zhuravleva, I. K.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 5; (1984); p. 982 - 985,874 - 876, View in Reaxys 48 of 108

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Partner (Liquid/Liquid Systems (MCS))

1-Decanol

Zhuravleva, I. K.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 5; (1984); p. 982 - 985,874 - 876, View in Reaxys 49 of 108

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Partner (Liquid/Liquid Systems (MCS))

1-undecanol

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Zhuravleva, I. K.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 5; (1984); p. 982 - 985,874 - 876, View in Reaxys 50 of 108

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Partner (Liquid/Liquid Systems (MCS))

1-dodecyl alcohol

Zhuravleva, I. K.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 5; (1984); p. 982 - 985,874 - 876, View in Reaxys 51 of 108

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Partner (Liquid/Liquid Systems (MCS))

1-tridecanol

Zhuravleva, I. K.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 5; (1984); p. 982 - 985,874 - 876, View in Reaxys 52 of 108

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Partner (Liquid/Liquid Systems (MCS))

n-pentadecyl alcohol; 2,2'-iminobis[ethanol]

Zhuravleva, I. K.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 5; (1984); p. 982 - 985,874 - 876, View in Reaxys 53 of 108

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Partner (Liquid/Liquid Systems (MCS))

n-pentadecyl alcohol

Zhuravleva, I. K.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 5; (1984); p. 982 - 985,874 - 876, View in Reaxys 54 of 108

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Partner (Liquid/Liquid Systems (MCS))

palmityl alcohol; 2,2'-iminobis[ethanol]

Zhuravleva, I. K.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 5; (1984); p. 982 - 985,874 - 876, View in Reaxys 55 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

16 - 30

Partner (Liquid/Liquid Systems (MCS))

hexan-1-ol; 1,1,2,2-tetrachloroethylene

Sazonov, V. P.; J. Appl. Chem. USSR (Engl. Transl.); vol. 55; nb. 3; (1982); p. 513 - 517,470 - 473, View in Reaxys 56 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25 - 140

Partner (Liquid/Liquid Systems (MCS))

cetane

Stryjek, Roman; Luszczyk, Marek; Fedorko-Antosik, Maria; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 29; nb. 3-4; (1981); p. 203 - 211, View in Reaxys 57 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Partner (Liquid/Liquid Systems (MCS))

nonyl alcohol; naphthalene

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Markuzin, N. P.; Sazonov, V. P.; Chernysheva, M. F.; J. Appl. Chem. USSR (Engl. Transl.); vol. 53; nb. 10; (1980); p. 2215 - 2219,1667 - 1672, View in Reaxys 58 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Partner (Liquid/Liquid Systems (MCS))

nonyl alcohol; H2O

Markuzin, N. P.; Sazonov, V. P.; Chernysheva, M. F.; J. Appl. Chem. USSR (Engl. Transl.); vol. 53; nb. 10; (1980); p. 2215 - 2219,1667 - 1672, View in Reaxys 59 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Partner (Liquid/Liquid Systems (MCS))

naphthalene; nonyl alcohol

Markuzin, N. P.; Sazonov, V. P.; Chernysheva, M. F.; J. Appl. Chem. USSR (Engl. Transl.); vol. 53; nb. 10; (1980); p. 2215 - 2219,1667 - 1672, View in Reaxys 60 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Partner (Liquid/Liquid Systems (MCS))

n-pentan-1-ol; glycerol

Zhuravleva, I. K.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 579 - 581; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1016 - 1018, View in Reaxys 61 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Partner (Liquid/Liquid Systems (MCS))

n-pentan-1-ol; glycerol

Zhuravleva, I. K.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 579 - 581; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1016 - 1018, View in Reaxys 62 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Partner (Liquid/Liquid Systems (MCS))

hexan-1-ol; glycerol

Zhuravleva, I. K.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 579 - 581; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1016 - 1018, View in Reaxys 63 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Partner (Liquid/Liquid Systems (MCS))

hexan-1-ol; glycerol

Zhuravleva, I. K.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 579 - 581; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1016 - 1018, View in Reaxys 64 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Partner (Liquid/Liquid Systems (MCS))

1-heptanol; glycerol

Zhuravleva, I. K.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 579 - 581; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1016 - 1018, View in Reaxys 65 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Partner (Liquid/Liquid Systems (MCS))

1-heptanol; glycerol

Zhuravleva, I. K.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 579 - 581; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1016 - 1018, View in Reaxys 66 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

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Partner (Liquid/Liquid Systems (MCS))

1-Octanol; glycerol

Zhuravleva, I. K.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 579 - 581; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1016 - 1018, View in Reaxys 67 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Partner (Liquid/Liquid Systems (MCS))

1-Octanol; glycerol

Zhuravleva, I. K.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 579 - 581; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1016 - 1018, View in Reaxys 68 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Partner (Liquid/Liquid Systems (MCS))

nonyl alcohol; glycerol

Zhuravleva, I. K.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 579 - 581; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1016 - 1018, View in Reaxys 69 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Partner (Liquid/Liquid Systems (MCS))

nonyl alcohol; glycerol

Zhuravleva, I. K.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 579 - 581; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1016 - 1018, View in Reaxys 70 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Partner (Liquid/Liquid Systems (MCS))

1-Decanol; glycerol

Zhuravleva, I. K.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 579 - 581; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1016 - 1018, View in Reaxys 71 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Partner (Liquid/Liquid Systems (MCS))

1-Decanol; glycerol

Zhuravleva, I. K.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 579 - 581; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1016 - 1018, View in Reaxys 72 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Partner (Liquid/Liquid Systems (MCS))

1-undecanol; glycerol

Zhuravleva, I. K.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 579 - 581; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1016 - 1018, View in Reaxys 73 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Partner (Liquid/Liquid Systems (MCS))

1-undecanol; glycerol

Zhuravleva, I. K.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 579 - 581; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1016 - 1018, View in Reaxys 74 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Partner (Liquid/Liquid Systems (MCS))

1-dodecyl alcohol; glycerol

Zhuravleva, I. K.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 579 - 581; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1016 - 1018, View in Reaxys

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75 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Partner (Liquid/Liquid Systems (MCS))

1-dodecyl alcohol; glycerol

Zhuravleva, I. K.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 579 - 581; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1016 - 1018, View in Reaxys 76 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Partner (Liquid/Liquid Systems (MCS))

1-tridecanol; glycerol

Zhuravleva, I. K.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 579 - 581; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1016 - 1018, View in Reaxys 77 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Partner (Liquid/Liquid Systems (MCS))

1-tridecanol; glycerol

Zhuravleva, I. K.; Russian Journal of Physical Chemistry; vol. 54; nb. 4; (1980); p. 579 - 581; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 4; (1980); p. 1016 - 1018, View in Reaxys 78 of 108

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Francis; Journal of Chemical and Engineering Data; vol. 10; (1965); p. 45,46, View in Reaxys; Sazonov; Chernysheva; J. Appl. Chem. USSR (Engl. Transl.); vol. 52; (1979); p. 2717,2572, View in Reaxys; Sazonov et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 50; (1977); p. 587,564,565, View in Reaxys; Franzosini et al.; Corsi e Seminari di Chimica, Consiglio Nazionale delle Ricerche e Fondazione "F. Giordani"; vol. 13; (1968); p. 26, View in Reaxys; Gopal; Chandra Sekhar; Anathakrishna; Ramachandra; Subramanyam; ; vol. 350; nb. 1660; (1976); p. 91 106, View in Reaxys; Sazonov; Russian Journal of Physical Chemistry; vol. 45; (1971); p. 264; ; p. 473, View in Reaxys; Sazonov; Zhilyaeva; Russian Journal of Physical Chemistry; vol. 45; (1971); p. 413; ; p. 733, View in Reaxys; Sazonov et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 49; (1976); p. 784,817, View in Reaxys; Sazonov et al.; Russian Journal of Physical Chemistry; vol. 48; (1974); p. 1700; ; p. 2891, View in Reaxys; Sazonov; Chernysheva; J. Gen. Chem. USSR (Engl. Transl.); vol. 48; (1978); p. 1682,1539, View in Reaxys 79 of 108

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Sazonov et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 52; (1979); p. 2710,2565, View in Reaxys; Sazonov; Russian Journal of Physical Chemistry; vol. 42; (1968); p. 1651; ; p. 3094, View in Reaxys; Sazonov et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 50; (1977); p. 587,564,565, View in Reaxys; Franzosini et al.; Ricerca Scientifica; vol. 38; (1968); p. 123, View in Reaxys; Sazonov et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 48; (1975); p. 1953,2025, View in Reaxys; Sazonov et al.; Russian Journal of Physical Chemistry; vol. 47; (1973); p. 271; ; p. 474, View in Reaxys; Sazonov; Zhilyaeva; Russian Journal of Physical Chemistry; vol. 47; (1973); p. 1383; ; p. 2444, View in Reaxys; Zhuravleva et al.; Russian Journal of Physical Chemistry; vol. 48; (1974); p. 1105; ; p. 1863, View in Reaxys; Zhuraveva et al.; Russian Journal of Physical Chemistry; vol. 48; (1974); p. 1104; ; p. 1863, View in Reaxys; Sazonov et al.; Russian Journal of Physical Chemistry; vol. 49; (1975); p. 946; ; p. 1594, View in Reaxys; Zhuravleva; Zhuravlev; Russian Journal of Physical Chemistry; vol. 49; (1975); p. 456; ; p. 778, View in Reaxys; Sazonov; Chernysheva; Russian Journal of Physical Chemistry; vol. 49; (1975); p. 1450; ; p. 2463, View in Reaxys; Zhuravleva et al.; Russian Journal of Physical Chemistry; vol. 49; (1975); p. 1530; ; p. 2609, View in Reaxys; Zhuravleva et al.; Russian Journal of Physical Chemistry; vol. 50; (1976); p. 237; ; p. 405, View in Reaxys; Zhuravleva et al.; Russian Journal of Physical Chemistry; vol. 51; (1977); p. 597; ; p. 1003, View in Reaxys; Zhuravleva et al.; Russian Journal of Physical Chemistry; vol. 51; (1977); p. 994; ; p. 1700, View in Reaxys; Sazonov et al.; Russian Journal of Physical Chemistry; vol. 51; (1977); p. 1266; ; p. 2150, View in Reaxys 80 of 108

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Malesinska; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 8; (1960); p. 53,54; Chem.Abstr.; nb. 1676g; (1957), View in Reaxys; Mel'nikova; Zhuravlev; Russian Journal of Physical Chemistry; vol. 39; (1965); p. 350; ; p. 664, View in Reaxys; Shuvawlew; Mel'nikowa; Russian Journal of Physical Chemistry; vol. 41; (1967); p. 844; Zhurnal Fizicheskoi Khimii; vol. 41; (1967); p. 1580, View in Reaxys; Sazonov; Chernysheva; J. Gen. Chem. USSR (Engl. Transl.); vol. 46; (1976); p. 997,993, View in Reaxys 81 of 108

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Currie,D.J. et al.; Canadian Journal of Chemistry; vol. 44; (1966); p. 1035 - 1043, View in Reaxys; Anderson et al.; Journal of Physical Chemistry; vol. 76; (1972); p. 4006,4008, View in Reaxys; Duraiswamy; Minard; Journal of

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Chemical and Engineering Data; vol. 18; (1973); p. 203,204,205, View in Reaxys; Rodina; Khaldna; Organic Reactivity (New York, English Translation); vol. 4; (1967); p. 74, View in Reaxys 82 of 108

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Schmid; Journal of the American Oil Chemists' Society; vol. 42; (1965); p. 372,373, View in Reaxys; Clever et al.; Journal of Chemical and Engineering Data; vol. 17; (1972); p. 31,33, View in Reaxys 83 of 108

Description (Liquid/ Liquid Systems (MCS))

Temperature of separation

Riccardi et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 23; (1968); p. 1816, View in Reaxys 84 of 108

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

56.3

Partner (Liquid/Liquid Systems (MCS))

1-Decanol

Francis; Journal of Physical Chemistry; vol. 60; (1956); p. 20,25, View in Reaxys 85 of 108

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

1-dodecyl alcohol

Francis; Journal of Physical Chemistry; vol. 60; (1956); p. 20,25, View in Reaxys 86 of 108

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

39.7

Partner (Liquid/Liquid Systems (MCS))

ethylene glycol

Francis; Journal of Physical Chemistry; vol. 60; (1956); p. 20,25, View in Reaxys 87 of 108

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

62.5

Partner (Liquid/Liquid Systems (MCS))

carbon disulfide

Francis; Journal of Physical Chemistry; vol. 60; (1956); p. 20,25, View in Reaxys 88 of 108

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

n-heptane; benzene

Kimura et al.; Kogyo Kagaku Zasshi; vol. 59; (1956); p. 1126; Chem.Abstr.; (1958); p. 13396, View in Reaxys 89 of 108

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

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Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

n-heptane; toluene

Kimura et al.; Kogyo Kagaku Zasshi; vol. 59; (1956); p. 1126; Chem.Abstr.; (1958); p. 13396, View in Reaxys 90 of 108

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

n-heptane; o-xylene

Kimura et al.; Kogyo Kagaku Zasshi; vol. 59; (1956); p. 1126; Chem.Abstr.; (1958); p. 13396, View in Reaxys 91 of 108

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

n-heptane; m-xylene

Kimura et al.; Kogyo Kagaku Zasshi; vol. 59; (1956); p. 1126; Chem.Abstr.; (1958); p. 13396, View in Reaxys 92 of 108

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

n-heptane; para-xylene

Kimura et al.; Kogyo Kagaku Zasshi; vol. 59; (1956); p. 1126; Chem.Abstr.; (1958); p. 13396, View in Reaxys 93 of 108

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

0 - 26

Partner (Liquid/Liquid Systems (MCS))

1-Decanol; ethylene glycol

Francis; Journal of Physical Chemistry; vol. 60; (1956); p. 20,25, View in Reaxys 94 of 108

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

16 - 29

Partner (Liquid/Liquid Systems (MCS))

1-dodecyl alcohol; ethylene glycol

Francis; Journal of Physical Chemistry; vol. 60; (1956); p. 20,25, View in Reaxys 95 of 108

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

21 - 26

Pressure (Liquid/Liquid Systems (MCS)) [Torr]

47808

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Comment (Liquid/Liquid Systems (MCS))

mit verschiedenen Kohlenwasserstoffen als dritter Komponente.

Partner (Liquid/Liquid Systems (MCS))

carbon dioxide

Francis; Journal of Physical Chemistry; vol. 58; (1954); p. 1099,1104, View in Reaxys 96 of 108

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

cyclohexane; benzene

Weck; Hunt; Industrial and Engineering Chemistry; vol. 46; (1954); p. 2521, View in Reaxys 97 of 108

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

octan-1-ol; H2O

Collander; Acta Chemica Scandinavica (1947-1973); vol. 5; (1951); p. 774,775, View in Reaxys 98 of 108

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Partner (Liquid/Liquid Systems (MCS))

water

Corelli; Aerotecnica; vol. 30; (1950); p. 32,36, View in Reaxys 99 of 108

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Partner (Liquid/Liquid Systems (MCS))

silver nitrate; cyclohexene

Salomon; Recueil des Travaux Chimiques des Pays-Bas; vol. 68; (1949); p. 903,904, View in Reaxys 100 of 108 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

olive oil; H2O

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Macy; J.ind.Hyg.; vol. 30; p. 140; Chem.Abstr.; (1948); p. 6619, View in Reaxys 101 of 108 Description (Liquid/ Liquid Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

Solution equilibrium isopropyl alcohol; water

Schumacher; Hunt; Industrial and Engineering Chemistry; vol. 34; (1942); p. 703, View in Reaxys 102 of 108 Description (Liquid/ Liquid Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

Solution equilibrium propan-1-ol; water

Fowler; Hunt; Industrial and Engineering Chemistry; vol. 33; (1941); p. 91, View in Reaxys 103 of 108 Description (Liquid/ Liquid Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

Critical solution temperature hexane; benzene

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Syono; J.Soc.chem.Ind.Japan Spl.; vol. 41; (1938); p. 236; Chem. Zentralbl.; vol. 110; nb. II; (1939); p. 1611, View in Reaxys 104 of 108 Description (Liquid/ Liquid Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

Critical solution temperature cyclohexane; benzene

Syono; J.Soc.chem.Ind.Japan Spl.; vol. 41; (1938); p. 236; Chem. Zentralbl.; vol. 110; nb. II; (1939); p. 1611, View in Reaxys 105 of 108 Description (Liquid/ Liquid Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

Critical solution temperature aliphatic acid

Broughton; Jones; Transactions of the Faraday Society; vol. 32; (1936); p. 686, View in Reaxys 106 of 108 Description (Liquid/ Liquid Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

Critical solution temperature hydrocarbon

Mulliken; Wakeman; Recueil des Travaux Chimiques des Pays-Bas; vol. 54; (1935); p. 366,369; Industrial and Engineering Chemistry, Analytical Edition; vol. 7; (1935); p. 276, View in Reaxys 107 of 108 Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

1,1,2,2-tetrachloroethylene

Cornish et al.; Industrial and Engineering Chemistry; vol. 26; (1934); p. 399, View in Reaxys 108 of 108 Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

63.3

Partner (Liquid/Liquid Systems (MCS))

CS2

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 558, View in Reaxys Liquid/Solid Systems (MCS) (6) 1 of 6

Description (Liquid/Solid Liquid/solid phase diagram Systems (MCS)) Zhuravleva et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 45; (1975); p. 1929,1894,1896, View in Reaxys; Sazonov; Chernysheva; J. Gen. Chem. USSR (Engl. Transl.); vol. 47; (1977); p. 534,489, View in Reaxys; Sazonov; Chernysheva; J. Appl. Chem. USSR (Engl. Transl.); vol. 51; (1978); p. 1019,981, View in Reaxys

2 of 6

Description (Liquid/Solid Liquid/solid phase diagram Systems (MCS)) Partner (Liquid/Solid Systems (MCS))

dinitrogen tetraoxide

Addison et al.; Journal of the Chemical Society; (1953); p. 2631,2632, View in Reaxys 3 of 6

Description (Liquid/Solid Eutectic Systems (MCS)) Temperature (Liquid/ Solid Systems (MCS)) [°C]

-36

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Partner (Liquid/Solid Systems (MCS))

benzene

Joukovsky; Bulletin des Societes Chimiques Belges; vol. 43; (1934); p. 401, View in Reaxys 4 of 6

Description (Liquid/Solid Eutectic Systems (MCS)) Temperature (Liquid/ Solid Systems (MCS)) [°C]

-42.3

Partner (Liquid/Solid Systems (MCS))

nitrobenzene

Joukovsky; Bulletin des Societes Chimiques Belges; vol. 43; (1934); p. 401, View in Reaxys 5 of 6

Description (Liquid/Solid Eutectic Systems (MCS)) Temperature (Liquid/ Solid Systems (MCS)) [°C]

-34

Partner (Liquid/Solid Systems (MCS))

formic acid

Joukovsky; Bulletin des Societes Chimiques Belges; vol. 43; (1934); p. 401, View in Reaxys 6 of 6

Description (Liquid/Solid Solidification diagram Systems (MCS)) Comment (Liquid/Solid Systems (MCS))

6 prozent Wasser; Verbindung 1:1.

Partner (Liquid/Solid Systems (MCS))

water; sulfuric acid

Liler; Symp.Hydrogen Bonding Ljubljana 1957 S.519,522,523, View in Reaxys Liquid/Vapour Systems (MCS) (240) 1 of 240

Description (Liquid/ Critical temperature Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

n-pentan-1-ol

Makowska, Anna; Szydlowski, Jerzy; Journal of Chemical and Engineering Data; vol. 50; nb. 4; (2005); p. 1365 1369, View in Reaxys 2 of 240

Description (Liquid/ Critical temperature Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

1-pentanol-d1

Makowska, Anna; Szydlowski, Jerzy; Journal of Chemical and Engineering Data; vol. 50; nb. 4; (2005); p. 1365 1369, View in Reaxys 3 of 240

Description (Liquid/ Critical temperature Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

ethylene glycol

Milewska; Siporska; Szydlowski; Polish Journal of Chemistry; vol. 78; nb. 4; (2004); p. 591 - 594, View in Reaxys 4 of 240

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

ethylene glycol

Milewska; Siporska; Szydlowski; Polish Journal of Chemistry; vol. 78; nb. 4; (2004); p. 591 - 594, View in Reaxys 5 of 240

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS))

154/412

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Temperature (Liquid/ 27.96 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

n-pentan-1-ol

Szydlowski; Milewska; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 505 - 508, View in Reaxys 6 of 240

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Temperature (Liquid/ 28.11 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1-pentanol-d1

Szydlowski; Milewska; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 505 - 508, View in Reaxys 7 of 240

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Temperature (Liquid/ 18.37 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

i-Butyl alcohol

Szydlowski; Milewska; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 505 - 508, View in Reaxys 8 of 240

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Temperature (Liquid/ 18.52 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

iso-BuOD

Szydlowski; Milewska; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 505 - 508, View in Reaxys 9 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 30 - 60 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1,1,1,2,2,3,3,4,4-Nonafluoro-docosane

Alessi, P.; Cortesi, A.; Napoli, M.; Conte, L.; Journal of Fluorine Chemistry; vol. 72; nb. 1; (1995); p. 43 - 48, View in Reaxys 10 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 30 - 60 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-docosane

Alessi, P.; Cortesi, A.; Napoli, M.; Conte, L.; Journal of Fluorine Chemistry; vol. 72; nb. 1; (1995); p. 43 - 48, View in Reaxys 11 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS))

155/412

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Temperature (Liquid/ 30 - 60 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluoro-octadecane

Alessi, P.; Cortesi, A.; Napoli, M.; Conte, L.; Journal of Fluorine Chemistry; vol. 72; nb. 1; (1995); p. 43 - 48, View in Reaxys 12 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 30 - 60 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-heptadecafluorohexadecane

Alessi, P.; Cortesi, A.; Napoli, M.; Conte, L.; Journal of Fluorine Chemistry; vol. 72; nb. 1; (1995); p. 43 - 48, View in Reaxys 13 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 30 - 60 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-Heptadecafluoro-icosane

Alessi, P.; Cortesi, A.; Napoli, M.; Conte, L.; Journal of Fluorine Chemistry; vol. 72; nb. 1; (1995); p. 43 - 48, View in Reaxys 14 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

cetane

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys; Dallas, Andrew J.; Carr, Peter W.; Journal of Physical Chemistry; vol. 98; nb. 18; (1994); p. 4927 - 4939, View in Reaxys 15 of 240

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 60 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

propan-1-ol

Bittrich, H.-J.; Eckert, R.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 185; nb. 2; (1994); p. 207 - 222, View in Reaxys 16 of 240

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 30 - 60 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

ethanol; H2O

Rezanova, E. N.; Toikka, A. M.; Markuzin, N. P.; Russian Journal of Applied Chemistry; vol. 66; nb. 4.1.; (1993); p. 686 - 690; Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation); vol. 66; nb. 4; (1993); p. 829 - 834, View in Reaxys

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17 of 240

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 30 - 60 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 80 - 337.4 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

H2O, CH3CH2OH

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

18β-glycyrrhizic acid

Stryjek, R.; Fras, Z; Polish Journal of Chemistry; vol. 66; nb. 7; (1992); p. 1175 - 1181, View in Reaxys 19 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

18β-Glycyrrhetinic acid

Stryjek, R.; Fras, Z; Polish Journal of Chemistry; vol. 66; nb. 7; (1992); p. 1175 - 1181, View in Reaxys 20 of 240

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 60 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

ethanol

Bittrich, H.-J.; Eckert, R.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 175; nb. 2; (1992); p. 217 - 234, View in Reaxys 21 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 24.9 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

EBBA

Burmistrov, V. A.; Aleksandriiskii, V. V.; Russian Journal of Physical Chemistry; vol. 65; nb. 7; (1991); p. 933 936; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p. 1754 - 1758, View in Reaxys 22 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 24.9 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

N-lt;4-n-Hexyloxy-benzylidengt;-4-methyl-anilin

157/412

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Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 24.9 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

4-ethoxybenzylidene-4'-heptanoyloxy-aniline

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 24.9 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

4-cyano-4'-n-pentyloxybiphenyl

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25.1 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

acetone

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 35; nb. 2; (1990); p. 156 - 162, View in Reaxys 26 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25.1 - 45.4 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

carbon disulfide

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 35; nb. 2; (1990); p. 156 - 162, View in Reaxys 27 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 55.3 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

ethyl acetate

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 35; nb. 2; (1990); p. 156 - 162, View in Reaxys 28 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 35.4 - 63.9 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

methanol

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 35; nb. 2; (1990); p. 156 - 162, View in Reaxys

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29 of 240

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

ethylene glycol

Salvi, Madhuri V.; Hook, W. Alexander Van; Journal of Physical Chemistry; vol. 94; nb. 20; (1990); p. 7812 - 7820, View in Reaxys 30 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 24.9 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

t-butyl bromide

Abraham, Michael H.; Grellier, Priscilla L.; Nasehzadeh, Asadollah; Walker, Rosemary A.C.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1988); p. 1717 - 1724, View in Reaxys 31 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 24.9 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

tertiary butyl chloride

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 30 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

benzene

Singh, P. P.; Dahiya, H. P.; Dagar, S.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 269; nb. 4; (1988); p. 817 - 831, View in Reaxys 33 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 30 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

toluene

Singh, P. P.; Dahiya, H. P.; Dagar, S.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 269; nb. 4; (1988); p. 817 - 831, View in Reaxys 34 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 35 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

o-xylene

Singh, P. P.; Dahiya, H. P.; Dagar, S.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 269; nb. 4; (1988); p. 817 - 831, View in Reaxys 35 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS))

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Temperature (Liquid/ 30 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

m-xylene

Singh, P. P.; Dahiya, H. P.; Dagar, S.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 269; nb. 4; (1988); p. 817 - 831, View in Reaxys 36 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

carbon disulfide

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 37 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

cyclohexane

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 38 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

triethylamine

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 39 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

diethyl ether

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 40 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

ethyl bromide

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 41 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS))

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Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

hexane

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 42 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

pentane

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 43 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

2-methyl-heptane

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 44 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

tetrahydrofuran

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 45 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

di-1-methylethyl ether

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 46 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

toluene

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 47 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS))

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Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

para-xylene

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 48 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

chloroform

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 49 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

tetrachloromethane

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 50 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

dibutyl ether

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 51 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

dichloromethane

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 52 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

decane

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 53 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS))

162/412

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Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

chlorobenzene

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 54 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

bromobenzene

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 55 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

monofluorobenzene

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 56 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

2,6-dimethylpyridine

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 57 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

2,6,10,15,19,23-hexamethyltetracosane

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 58 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

Hexafluorobenzene

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 59 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS))

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Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

phenetole

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 60 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

.alpha.-picoline

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 61 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1,2-DICHLOROETHANE

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 62 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

ethyl acetate

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 63 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

iodobenzene

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 64 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

3,6,9-trioxadodecane

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 65 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS))

164/412

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Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

methoxybenzene

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 66 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1-Octanol

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 67 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

cyclohexanone

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 68 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

tert-butanol

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 69 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

i-Amyl alcohol

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 70 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

pyridine

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 71 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS))

165/412

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Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1,4-dioxane

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 72 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

isopropyl alcohol

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 73 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

propan-1-ol

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 74 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

acetone

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 75 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

benzonitrile

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 76 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

benzyl Ether

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 77 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS))

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Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

acetophenone

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 78 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

tris(dimethylamino)phosphine oxide

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 79 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

ethanol

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 80 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

nitrobenzene

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 81 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

m-cresol

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 82 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

DMAA

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 83 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS))

167/412

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Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

acetic acid

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 84 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

methanol

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 85 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

benzyl alcohol

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 86 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

DMFA

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 87 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

2-methoxy-ethanol

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 88 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

N-Methyl-2-pyrrolidone

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 89 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS))

168/412

2016-04-19 03:35:30

Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

propyl cyanide

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 90 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1-cyanooctane

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 91 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

nitrile of pentadecanoic acid

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 92 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

aniline

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 93 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

4-butanolide

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 94 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

dimethyl sulfoxide

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 95 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS))

169/412

2016-04-19 03:35:30

Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

diethylene glycol

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 96 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

ethylene glycol

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 97 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

H2O

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 98 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

diiodomethane

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 99 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

2,2,2-trifluoroethanol

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 100 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1,1,1,3',3',3'-hexafluoro-propanol

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 101 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS))

170/412

2016-04-19 03:35:30

Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

perfluorohexane

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 102 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

octanol

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 103 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

butanone

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 104 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

n-heptane

Afrashtehfar, Shapour; Cave, Genille C. B.; Canadian Journal of Chemistry; vol. 64; (1986); p. 198 - 203, View in Reaxys; Milanova, Etela; Cave, Genille C.; Canadian Journal of Chemistry; vol. 60; (1982); p. 2697 - 2706, View in Reaxys 105 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1-heptene

Afrashtehfar, Shapour; Cave, Genille C. B.; Canadian Journal of Chemistry; vol. 64; (1986); p. 198 - 203, View in Reaxys 106 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1,6--heptadiene

Afrashtehfar, Shapour; Cave, Genille C. B.; Canadian Journal of Chemistry; vol. 64; (1986); p. 198 - 203, View in Reaxys 107 of 240 Description (Liquid/ Critical data for mixtures Vapour Systems (MCS))

171/412

2016-04-19 03:35:30

Temperature (Liquid/ 56.6 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

ethylene glycol; 1,1,2,2-tetrachloroethylene

Sazonov, V. P.; J. Appl. Chem. USSR (Engl. Transl.); vol. 59; nb. 1; (1986); p. 12 - 18,10 - 15, View in Reaxys 108 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

isopropyl alcohol; H2O

Sazonov; Journal of applied chemistry of the USSR; vol. 59; nb. 7 pt 1; (1986); p. 1348 - 1352, View in Reaxys 109 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 298.2 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1-Octanol

Hussam; Carr; Analytical Chemistry; vol. 57; nb. 4; (1985); p. 793 - 801, View in Reaxys 110 of 240

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 24.9 - 125 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

dichloromethane

Srivastava, Rakesh; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 30; nb. 3; (1985); p. 313 318, View in Reaxys 111 of 240

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 24.9 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

dichloromethane

Srivastava, Rakesh; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 30; nb. 3; (1985); p. 313 318, View in Reaxys 112 of 240

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 74.8 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

dichloromethane

Srivastava, Rakesh; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 30; nb. 3; (1985); p. 313 318, View in Reaxys 113 of 240

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 125 Vapour Systems (MCS)) [°C]

172/412

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Partner (Liquid/Vapour Systems (MCS))

dichloromethane

Srivastava, Rakesh; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 30; nb. 3; (1985); p. 313 318, View in Reaxys 114 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 24.9 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

dichloromethane

Srivastava, Rakesh; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 30; nb. 3; (1985); p. 313 318, View in Reaxys 115 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 74.8 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

dichloromethane

Srivastava, Rakesh; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 30; nb. 3; (1985); p. 313 318, View in Reaxys 116 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 125 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

dichloromethane

Srivastava, Rakesh; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 30; nb. 3; (1985); p. 313 318, View in Reaxys 117 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 40 - 60 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

octanol

Belfer; Locke; Analytical Chemistry; vol. 56; nb. 13; (1984); p. 2485 - 2489, View in Reaxys 118 of 240

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 290.1 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

hexan-1-ol; 1,1,2,2-tetrachloroethylene

Sazonov, V.P.; J. Appl. Chem. USSR (Engl. Transl.); vol. 57; nb. 1; (1984); p. 7 - 13,5 - 10, View in Reaxys 119 of 240

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 293.2 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

hexan-1-ol; 1,1,2,2-tetrachloroethylene

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Sazonov, V.P.; J. Appl. Chem. USSR (Engl. Transl.); vol. 57; nb. 1; (1984); p. 7 - 13,5 - 10, View in Reaxys 120 of 240 Description (Liquid/ Liquid/vapour phase diagram Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

hexan-1-ol; 1,1,2,2-tetrachloroethylene

Sazonov, V.P.; J. Appl. Chem. USSR (Engl. Transl.); vol. 57; nb. 1; (1984); p. 7 - 13,5 - 10, View in Reaxys 121 of 240 Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

hexan-1-ol; 1,1,2,2-tetrachloroethylene

Sazonov, V.P.; J. Appl. Chem. USSR (Engl. Transl.); vol. 57; nb. 1; (1984); p. 7 - 13,5 - 10, View in Reaxys 122 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 290.1 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1,1,2,2-tetrachloroethylene; hexan-1-ol

Sazonov, V.P.; J. Appl. Chem. USSR (Engl. Transl.); vol. 57; nb. 1; (1984); p. 7 - 13,5 - 10, View in Reaxys 123 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 293.2 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1,1,2,2-tetrachloroethylene; hexan-1-ol

Sazonov, V.P.; J. Appl. Chem. USSR (Engl. Transl.); vol. 57; nb. 1; (1984); p. 7 - 13,5 - 10, View in Reaxys 124 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 50 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

petroleum sulfoxides

Kozin; Diyarov; Komleva; Antoshkova; Journal of applied chemistry of the USSR; vol. 57; nb. 5 pt 2; (1984); p. 1007 - 1010, View in Reaxys 125 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 50 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

butyl sulfoxide

Kozin; Diyarov; Komleva; Antoshkova; Journal of applied chemistry of the USSR; vol. 57; nb. 5 pt 2; (1984); p. 1007 - 1010, View in Reaxys 126 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 80 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

diphenyl sulphoxide

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Kozin; Diyarov; Komleva; Antoshkova; Journal of applied chemistry of the USSR; vol. 57; nb. 5 pt 2; (1984); p. 1007 - 1010, View in Reaxys 127 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 50 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

petroleum sulfones

Kozin; Diyarov; Komleva; Antoshkova; Journal of applied chemistry of the USSR; vol. 57; nb. 5 pt 2; (1984); p. 1007 - 1010, View in Reaxys 128 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 50 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

2,4-dimethyl sulfolane

Kozin; Diyarov; Komleva; Antoshkova; Journal of applied chemistry of the USSR; vol. 57; nb. 5 pt 2; (1984); p. 1007 - 1010, View in Reaxys 129 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 50 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

petroleum sulfides

Kozin; Diyarov; Komleva; Antoshkova; Journal of applied chemistry of the USSR; vol. 57; nb. 5 pt 2; (1984); p. 1007 - 1010, View in Reaxys 130 of 240 Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

palmityl alcohol

Zhuravleva, I. K.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 5; (1984); p. 982 - 985,874 - 876, View in Reaxys 131 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 35.9 - 94.8 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

ethyl acetate

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 132 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 35.9 - 94.9 Systems (MCS)) [Torr]

175/412

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Partner (Liquid/Vapour Systems (MCS))

ethyl acetate

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 133 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 75.1 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 317.2 - 713.007 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

ethyl acetate

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 134 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 75.1 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 317.2 - 713.2 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

ethyl acetate

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 135 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 125 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 1508.6 - 2958.2 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

ethyl acetate

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 136 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 125 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 1508.6 - 2958.8 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

ethyl acetate

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 137 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C]

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Pressure (Liquid/Vapour 35.9 - 89 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

acetonitrile

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 138 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 35.9 - 89 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

acetonitrile

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 139 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 75 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 316.4 - 617.7 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

acetonitrile

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 140 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 75 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 316.4 - 617.8 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

acetonitrile

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 141 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 125 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 1506.05 - 2534.5 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

acetonitrile

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 142 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS))

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Temperature (Liquid/ 125 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 1506.06 - 2534.9 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

acetonitrile

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 143 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 35.9 - 231.6 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

acetone

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 144 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 35.9 - 231.6 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

acetone

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 145 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 75 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 316.2 - 1397.2 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

acetone

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 146 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 75 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 316.1 - 1397.3 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

acetone

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys

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147 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ -76 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 1464.9 - 4983.4 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

acetone

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 148 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ -76 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 1465.2 - 4983.6 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

acetone

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 149 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 35.9 - 107.3 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

n-Butyl chloride

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 150 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 35.9 - 107.1 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

n-Butyl chloride

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 151 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 75 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 316.3 - 723.4 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

n-Butyl chloride

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Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 152 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 75 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 316.3 - 723.4 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

n-Butyl chloride

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 153 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 125 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 1506.05 - 2835.2 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

n-Butyl chloride

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 154 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 125 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 1506.05 - 2831.4 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

n-Butyl chloride

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 155 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 12.2 - 37.2 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

chlorobenzene

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 156 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 12.2 - 37.1 Systems (MCS)) [Torr]

180/412

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Partner (Liquid/Vapour Systems (MCS))

chlorobenzene

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 157 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 75 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 122.6 - 324.3 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

chlorobenzene

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 158 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 75 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 122.6 - 324.1 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

chlorobenzene

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 159 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 125.1 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 636.1 - 1535.2 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

chlorobenzene

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 160 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 125.1 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 636.09 - 1534.5 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

chlorobenzene

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 113 - 119, View in Reaxys 161 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C]

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Pressure (Liquid/Vapour 35.8 - 130.8 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

methanol

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 119 - 123, View in Reaxys 162 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 35.8 - 130.8 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

methanol

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 119 - 123, View in Reaxys 163 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 75 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 314.9 - 1134.6 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

methanol

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 119 - 123, View in Reaxys 164 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 75 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 314.8 - 1135.7 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

methanol

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 119 - 123, View in Reaxys 165 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 115.1 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 1136.9 - 4184.6 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

methanol

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 119 - 123, View in Reaxys 166 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS))

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Temperature (Liquid/ 115.1 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 1136.9 - 4184.8 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

methanol

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 119 - 123, View in Reaxys 167 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 35.9 - 76.6 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

ethanol

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 119 - 123, View in Reaxys 168 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 35.9 - 76.6 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

ethanol

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 119 - 123, View in Reaxys 169 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 75 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 316 - 731.7 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

ethanol

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 119 - 123, View in Reaxys 170 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 75 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 316 - 731.3 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

ethanol

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 119 - 123, View in Reaxys

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171 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 125 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 1506.3 - 3780.3 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

ethanol

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 119 - 123, View in Reaxys 172 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 125 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 1506.3 - 3780.8 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

ethanol

Khurma, Jagjit R.; Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 1; (1983); p. 119 - 123, View in Reaxys 173 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

benzene

Milanova, Etela; Cave, Genille C.; Canadian Journal of Chemistry; vol. 60; (1982); p. 2697 - 2706, View in Reaxys 174 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

tetrachloromethane

Milanova, Etela; Cave, Genille C.; Canadian Journal of Chemistry; vol. 60; (1982); p. 2697 - 2706, View in Reaxys 175 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

benzene

Anantaraman, A.V.; Goldman, Saul; Canadian Journal of Chemistry; vol. 58; (1980); p. 1183 - 1187, View in Reaxys; Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 176 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

butan-1-ol

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 177 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS))

184/412

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Partner (Liquid/Vapour Systems (MCS))

n-heptane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 178 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

2,2,4-trimethylpentane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 179 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

octanol

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 180 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

1-Octanol

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 181 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

toluene

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 182 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

n-Butyl chloride

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 183 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

tetrachloromethane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 184 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

chloroform

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 185 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

dichloromethane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys

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186 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

methyl iodide

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 187 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

ethyl bromide

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 188 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

ethyl iodide

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 189 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

1-Chloropropane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 190 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

tertiary butyl chloride

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 191 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

isoprene

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 192 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

cyclohexane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 193 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

hexane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 194 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

triethylamine

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Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 195 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 39 - 44 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

cetane

Alessi, Paolo; Kikic, Ireneo; Nonino, Carlo; Visalberghi, Mirella Orlandini; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 448 - 450, View in Reaxys 196 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 51 - 79 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

α-octadecene

Alessi, Paolo; Kikic, Ireneo; Nonino, Carlo; Visalberghi, Mirella Orlandini; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 448 - 450, View in Reaxys 197 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 51 - 82 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

tetracosan acid

Alessi, Paolo; Kikic, Ireneo; Nonino, Carlo; Visalberghi, Mirella Orlandini; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 448 - 450, View in Reaxys 198 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 44 - 55.5 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1-Chlorohexadecan

Alessi, Paolo; Kikic, Ireneo; Nonino, Carlo; Visalberghi, Mirella Orlandini; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 448 - 450, View in Reaxys 199 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 41 - 64.2 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1-chlorooctadecane

Alessi, Paolo; Kikic, Ireneo; Nonino, Carlo; Visalberghi, Mirella Orlandini; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 448 - 450, View in Reaxys 200 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 35 - 60 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1-dodecyl alcohol

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Alessi, Paolo; Kikic, Ireneo; Nonino, Carlo; Visalberghi, Mirella Orlandini; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 448 - 450, View in Reaxys 201 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 44.8 - 75.8 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1-tetradecanol

Alessi, Paolo; Kikic, Ireneo; Nonino, Carlo; Visalberghi, Mirella Orlandini; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 448 - 450, View in Reaxys 202 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 36 - 50.4 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

decyl methyl ketone

Alessi, Paolo; Kikic, Ireneo; Nonino, Carlo; Visalberghi, Mirella Orlandini; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 448 - 450, View in Reaxys 203 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 57.7 - 70.8 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

bis-octyl ketone

Alessi, Paolo; Kikic, Ireneo; Nonino, Carlo; Visalberghi, Mirella Orlandini; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 448 - 450, View in Reaxys 204 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 61.4 - 91.5 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

10-Nonadecanon

Alessi, Paolo; Kikic, Ireneo; Nonino, Carlo; Visalberghi, Mirella Orlandini; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 448 - 450, View in Reaxys 205 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 41.6 - 77.1 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

butanone

Thomas, Eugene R.; Newman, Bruce A.; Nicolaides, George L.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 233 - 240, View in Reaxys 206 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 41.8 - 75.9 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

tetrachloromethane

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Thomas, Eugene R.; Newman, Bruce A.; Nicolaides, George L.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 233 - 240, View in Reaxys 207 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 46.6 - 58.8 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

methylene chloride

Thomas, Eugene R.; Newman, Bruce A.; Nicolaides, George L.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 233 - 240, View in Reaxys 208 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 45.4 - 82.1 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1,2-DICHLOROETHANE

Thomas, Eugene R.; Newman, Bruce A.; Nicolaides, George L.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 233 - 240, View in Reaxys 209 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 38.6 - 74.1 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

ethyl acetate

Thomas, Eugene R.; Newman, Bruce A.; Nicolaides, George L.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 233 - 240, View in Reaxys 210 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 49.8 - 67.8 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

hexane

Thomas, Eugene R.; Newman, Bruce A.; Nicolaides, George L.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 233 - 240, View in Reaxys 211 of 240

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 75.6 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

triethylamine

Thomas, Eugene R.; Newman, Bruce A.; Nicolaides, George L.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 233 - 240, View in Reaxys 212 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 45.1 - 98.4 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

benzene

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Thomas, Eugene R.; Newman, Bruce A.; Nicolaides, George L.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 233 - 240, View in Reaxys 213 of 240 Description (Liquid/ Liquid/vapour phase diagram Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

hexan-1-ol; water

Sazonov, V. P.; J. Gen. Chem. USSR (Engl. Transl.); vol. 52; nb. 8; (1982); p. 1697 - 1702,1501 - 1505, View in Reaxys 214 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 29.9 - 69.9 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

cetane

Stryjek, Roman; Luszczyk, Marek; Fedorko-Antosik, Maria; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 29; nb. 3-4; (1981); p. 203 - 211, View in Reaxys 215 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Stadnicki; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 11; (1963); p. 293,296, View in Reaxys; Brown; Smith; Australian Journal of Chemistry; vol. 13; (1960); p. 30, View in Reaxys; Schuberth; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 225; (1964); p. 305,307, View in Reaxys; Saunders; Spaull; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 28; (1961); p. 332,337, View in Reaxys; Marsh et al.; Journal of Chemical Thermodynamics; vol. 11; (1979); p. 897,899 - 901, View in Reaxys 216 of 240 Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Fischer et al.; Pharmazeutische Zentralhalle; vol. 105; (1966); p. 73,74, View in Reaxys; Fischer et al.; Pharmazeutische Zentralhalle; vol. 99; (1960); p. 299,310, View in Reaxys; Das; Griffiths; Journal of Chemical Physics; vol. 70; (1979); p. 5555, View in Reaxys; Anisimov et al.; Russian Journal of Physical Chemistry; vol. 44; (1970); p. 19; ; p. 34, View in Reaxys; Anisimov; Beridze; Russian Journal of Physical Chemistry; vol. 44; (1970); p. 344; ; p. 617, View in Reaxys; Alwani; Schneider; Berichte der Bunsen-Gesellschaft; vol. 80; (1976); p. 1310,1311, View in Reaxys 217 of 240 Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Gerster et al.; Journal of Chemical and Engineering Data; vol. 5; (1960); p. 423,425, View in Reaxys; Stadnicki; Roczniki Chemii; vol. 38; (1964); p. 827, View in Reaxys; Nakanishi et al.; Journal of Chemical and Engineering Data; vol. 13; (1968); p. 188, View in Reaxys; Burova et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 38; (1965); p. 121,111, View in Reaxys; Gorbunov; Susarev; J. Appl. Chem. USSR (Engl. Transl.); vol. 41; (1968); p. 2680,2522, View in Reaxys; Schuberth; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 225; (1964); p. 305,307, View in Reaxys; Ogoridnikow; Kogan; Nemzow; J. Appl. Chem. USSR (Engl. Transl.); vol. 34; (1961); p. 841,807; Chem.Abstr.; nb. 1419; (1963), View in Reaxys; Tolstova et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 38; (1965); p. 2617,2558, View in Reaxys; Wong; Eckert; Journal of Chemical and Engineering Data; vol. 14; (1969); p. 432, View in Reaxys; Sazonov et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 50; (1977); p. 1524,1469, View in Reaxys; Schuberth; Kraenke; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 245; (1970); p. 49,60, View in Reaxys; Sazonov et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 50; (1977); p. 455,438, View in Reaxys; Kudryavtseva; Eizen; J. Appl. Chem. USSR (Engl. Transl.); vol. 43; (1970); p. 708,716, View in Reaxys 218 of 240 Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Fillipov et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 50; (1977); p. 1321,1269, View in Reaxys; Dahlberg; Long; Journal of the American Chemical Society; vol. 95; (1973); p. 3825,3827, 3830, View in Reaxys; Derrick; Clever; Journal of Physical Chemistry; vol. 75; (1971); p. 3728, View in Reaxys; Aleksandrov; Chernyi; Russian Journal of Physical Chemistry; vol. 50; (1976); p. 299; ; p. 516, View in Reaxys 219 of 240 Description (Liquid/ Boiling points of mixtures Vapour Systems (MCS)) Ogoridnikow; Kogan; Nemzow; J. Appl. Chem. USSR (Engl. Transl.); vol. 34; (1961); p. 841,807; Chem.Abstr.; nb. 1419; (1963), View in Reaxys; Marinichev; Vertsman; J. Appl. Chem. USSR (Engl. Transl.); vol. 46; (1973); p. 355,368, View in Reaxys

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220 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 0 Vapour Systems (MCS)) [°C] Comment (Liquid/ Diagramm. Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

dinitrogen tetraoxide

Addison; Sheldon; Journal of the Chemical Society; (1957); p. 1937,1940, View in Reaxys 221 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ -10 - 10 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

dinitrogen tetraoxide

Addison; Sheldon; Journal of the Chemical Society; (1957); p. 1937,1940, View in Reaxys 222 of 240 Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 45 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

tetrachloromethane

Brown; Smith; Australian Journal of Chemistry; vol. 8; (1955); p. 501,503, View in Reaxys 223 of 240 Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 45 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

benzene

Brown; Smith; Australian Journal of Chemistry; vol. 8; (1955); p. 501,503, View in Reaxys 224 of 240 Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 60 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

acetonitrile

Brown; Smith; Australian Journal of Chemistry; vol. 8; (1955); p. 62,65, View in Reaxys 225 of 240 Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Pressure (Liquid/Vapour 760 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

benzene

Weck; Hunt; Industrial and Engineering Chemistry; vol. 46; (1954); p. 2521, View in Reaxys 226 of 240 Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

cyclohexane; benzene

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Weck; Hunt; Industrial and Engineering Chemistry; vol. 46; (1954); p. 2521, View in Reaxys 227 of 240 Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Pressure (Liquid/Vapour 54.6 - 400 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

Nitroethane

Cantoni; Feldman; Industrial and Engineering Chemistry; vol. 45; (1953); p. 2580, View in Reaxys 228 of 240 Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Pressure (Liquid/Vapour 760 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

methanol

Desseigne; Belliot; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 49; (1952); p. 46, View in Reaxys 229 of 240 Description (Liquid/ Partial pressures of the components Vapour Systems (MCS)) Comment (Liquid/ Nitromethan-Partialdruck ueber binaeren Gemischen mit unverzweigten Alkansaeuren. Vapour Systems (MCS)) Jones; Saunders; Journal of the Chemical Society; (1951); p. 2944,2946,2947, View in Reaxys 230 of 240 Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

water

Schumacher; Hunt; Industrial and Engineering Chemistry; vol. 34; (1942); p. 703, View in Reaxys; Fowler; Hunt; Industrial and Engineering Chemistry; vol. 33; (1941); p. 91, View in Reaxys 231 of 240 Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

isopropyl alcohol

Schumacher; Hunt; Industrial and Engineering Chemistry; vol. 34; (1942); p. 703, View in Reaxys 232 of 240 Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

isopropyl alcohol; water

Schumacher; Hunt; Industrial and Engineering Chemistry; vol. 34; (1942); p. 703, View in Reaxys 233 of 240 Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

propan-1-ol

Fowler; Hunt; Industrial and Engineering Chemistry; vol. 33; (1941); p. 91, View in Reaxys 234 of 240 Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

water; propan-1-ol

Fowler; Hunt; Industrial and Engineering Chemistry; vol. 33; (1941); p. 91, View in Reaxys 235 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

diethyl ether

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Joukovsky; Bulletin des Societes Chimiques Belges; vol. 43; (1934); p. 401, View in Reaxys 236 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

CS2

Joukovsky; Bulletin des Societes Chimiques Belges; vol. 43; (1934); p. 401, View in Reaxys 237 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

methanol

Joukovsky; Bulletin des Societes Chimiques Belges; vol. 43; (1934); p. 401, View in Reaxys 238 of 240 Description (Liquid/ Partial pressures of the components Vapour Systems (MCS)) Comment (Liquid/ zur Bestimmung der Partialdrucke im binaeren System mit Aether. Vapour Systems (MCS)) Joukowsky; Bulletin des Societes Chimiques Belges; vol. 43; (1934); p. 314, View in Reaxys 239 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 15 - 65 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

water

Williams; Journal of the American Chemical Society; vol. 47; (1925); p. 2646, View in Reaxys 240 of 240 Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

ethyl iodide

v.Halban; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 84; (1913); p. 139, View in Reaxys Magnetic Susceptibility (1) References Baddar; Sugden; Journal of the Chemical Society; (1950); p. 308,311, View in Reaxys; Witanowski et al.; Journal of Magnetic Resonance (1969-1992); vol. 28; (1977); p. 217,218, View in Reaxys; Borovikov; Egorov; Theoretical and Experimental Chemistry; vol. 7; (1971); p. 539,540; ; p. 251, View in Reaxys; Francois; Bulletin de la Societe Chimique de France; (1962); p. 511, View in Reaxys Mechanical & Physical Properties (MCS) (58) 1 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

24.85 - 39.85

Pressure (Mechanical & Physical Properties (MCS)) [Torr]

3750.3 - 53779.3

Partner (Mechanical & Physical Properties (MCS))

carbon dioxide

Lazzaroni, Michael J.; Bush, David; Brown, James S.; Eckert, Charles A.; Journal of Chemical and Engineering Data; vol. 50; nb. 1; (2005); p. 60 - 65, View in Reaxys 2 of 58

Description (Mechanical & Physical Properties (MCS))

Ultrasonic velocity

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Comment (Mechanical & Physical Properties (MCS))

temperature dependence

Partner (Mechanical & Physical Properties (MCS))

n-pentan-1-ol

Makowska, Anna; Szydlowski, Jerzy; Journal of Chemical and Engineering Data; vol. 50; nb. 4; (2005); p. 1365 1369, View in Reaxys 3 of 58

Description (Mechanical & Physical Properties (MCS))

Ultrasonic velocity

Comment (Mechanical & Physical Properties (MCS))

temperature dependence

Partner (Mechanical & Physical Properties (MCS))

1-pentanol-d1

Makowska, Anna; Szydlowski, Jerzy; Journal of Chemical and Engineering Data; vol. 50; nb. 4; (2005); p. 1365 1369, View in Reaxys 4 of 58

Description (Mechanical & Physical Properties (MCS))

Adiabatic compressibility

Comment (Mechanical & Physical Properties (MCS))

temperature dependence. Object(s) of Study: diagram

Partner (Mechanical & Physical Properties (MCS))

n-pentan-1-ol

Makowska, Anna; Szydlowski, Jerzy; Journal of Chemical and Engineering Data; vol. 50; nb. 4; (2005); p. 1365 1369, View in Reaxys 5 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Comment (Mechanical & Physical Properties (MCS))

temperature dependence. Object(s) of Study: diagram

Partner (Mechanical & Physical Properties (MCS))

n-pentan-1-ol

Makowska, Anna; Szydlowski, Jerzy; Journal of Chemical and Engineering Data; vol. 50; nb. 4; (2005); p. 1365 1369, View in Reaxys 6 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Comment (Mechanical & Physical Properties (MCS))

concentration dependence

Partner (Mechanical & Physical Properties (MCS))

methanol

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys

194/412

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7 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Comment (Mechanical & Physical Properties (MCS))

concentration dependence

Partner (Mechanical & Physical Properties (MCS))

ethanol

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 8 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Comment (Mechanical & Physical Properties (MCS))

concentration dependence

Partner (Mechanical & Physical Properties (MCS))

propan-1-ol

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 9 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Comment (Mechanical & Physical Properties (MCS))

concentration dependence

Partner (Mechanical & Physical Properties (MCS))

isopropyl alcohol

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 10 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Comment (Mechanical & Physical Properties (MCS))

concentration dependence

Partner (Mechanical & Physical Properties (MCS))

butan-1-ol

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys

195/412

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11 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Comment (Mechanical & Physical Properties (MCS))

concentration dependence

Partner (Mechanical & Physical Properties (MCS))

i-Butyl alcohol

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 12 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Comment (Mechanical & Physical Properties (MCS))

concentration dependence

Partner (Mechanical & Physical Properties (MCS))

acetone

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 13 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Comment (Mechanical & Physical Properties (MCS))

concentration dependence

Partner (Mechanical & Physical Properties (MCS))

butanone

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 14 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Comment (Mechanical & Physical Properties (MCS))

concentration dependence

Partner (Mechanical & Physical Properties (MCS))

acetic acid methyl ester

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys

196/412

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15 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Comment (Mechanical & Physical Properties (MCS))

concentration dependence

Partner (Mechanical & Physical Properties (MCS))

ethyl acetate

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 16 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Comment (Mechanical & Physical Properties (MCS))

concentration dependence

Partner (Mechanical & Physical Properties (MCS))

tetrachloromethane

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 17 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Comment (Mechanical & Physical Properties (MCS))

concentration dependence

Partner (Mechanical & Physical Properties (MCS))

benzene

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 18 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Comment (Mechanical & Physical Properties (MCS))

concentration dependence

Partner (Mechanical & Physical Properties (MCS))

toluene

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys

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19 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

20 - 40

Pressure (Mechanical & Physical Properties (MCS)) [Torr]

760

Partner (Mechanical & Physical Properties (MCS))

methanol

Tu; Lee; Peng; Journal of Chemical and Engineering Data; vol. 46; nb. 1; (2001); p. 151 - 155, View in Reaxys 20 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

20 - 40

Pressure (Mechanical & Physical Properties (MCS)) [Torr]

760

Partner (Mechanical & Physical Properties (MCS))

ethanol

Tu; Lee; Peng; Journal of Chemical and Engineering Data; vol. 46; nb. 1; (2001); p. 151 - 155, View in Reaxys 21 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

20 - 40

Pressure (Mechanical & Physical Properties (MCS)) [Torr]

760

Partner (Mechanical & Physical Properties (MCS))

propan-1-ol

Tu; Lee; Peng; Journal of Chemical and Engineering Data; vol. 46; nb. 1; (2001); p. 151 - 155, View in Reaxys 22 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

20 - 40

Pressure (Mechanical & Physical Properties (MCS)) [Torr]

760

Partner (Mechanical & Physical Properties (MCS))

isopropyl alcohol

Tu; Lee; Peng; Journal of Chemical and Engineering Data; vol. 46; nb. 1; (2001); p. 151 - 155, View in Reaxys 23 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

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Temperature (Mechanical & Physical Properties (MCS)) [°C]

20 - 40

Pressure (Mechanical & Physical Properties (MCS)) [Torr]

760

Partner (Mechanical & Physical Properties (MCS))

iso-butanol

Tu; Lee; Peng; Journal of Chemical and Engineering Data; vol. 46; nb. 1; (2001); p. 151 - 155, View in Reaxys 24 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

20 - 40

Pressure (Mechanical & Physical Properties (MCS)) [Torr]

760

Partner (Mechanical & Physical Properties (MCS))

tert-butanol

Tu; Lee; Peng; Journal of Chemical and Engineering Data; vol. 46; nb. 1; (2001); p. 151 - 155, View in Reaxys 25 of 58

Description (Mechanical & Physical Properties (MCS))

Excess partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

butan-1-ol

Romani; Troncoso; Tovar; Cerdeirina; Carballo; Journal of Chemical and Engineering Data; vol. 46; nb. 2; (2001); p. 312 - 316, View in Reaxys 26 of 58

Description (Mechanical & Physical Properties (MCS))

Excess partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

i-Butyl alcohol

Romani; Troncoso; Tovar; Cerdeirina; Carballo; Journal of Chemical and Engineering Data; vol. 46; nb. 2; (2001); p. 312 - 316, View in Reaxys 27 of 58

Description (Mechanical & Physical Properties (MCS))

Excess partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

iso-butanol

Romani; Troncoso; Tovar; Cerdeirina; Carballo; Journal of Chemical and Engineering Data; vol. 46; nb. 2; (2001); p. 312 - 316, View in Reaxys

199/412

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28 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

20 - 40

Partner (Mechanical & Physical Properties (MCS))

acetic acid methyl ester

Lee; Tu; Journal of Chemical and Engineering Data; vol. 44; nb. 1; (1999); p. 108 - 111, View in Reaxys 29 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

20 - 40

Partner (Mechanical & Physical Properties (MCS))

ethyl acetate

Lee; Tu; Journal of Chemical and Engineering Data; vol. 44; nb. 1; (1999); p. 108 - 111, View in Reaxys 30 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

20 - 40

Partner (Mechanical & Physical Properties (MCS))

1-Propyl acetate

Lee; Tu; Journal of Chemical and Engineering Data; vol. 44; nb. 1; (1999); p. 108 - 111, View in Reaxys 31 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

20 - 40

Partner (Mechanical & Physical Properties (MCS))

acetic acid butyl ester

Lee; Tu; Journal of Chemical and Engineering Data; vol. 44; nb. 1; (1999); p. 108 - 111, View in Reaxys 32 of 58

Description (Mechanical & Physical Properties (MCS))

Excess partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

isopropyl alcohol

Sharma; Singh, Jaibir; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 38; nb. 1; (1999); p. 65 - 69, View in Reaxys 33 of 58

Description (Mechanical & Physical Properties (MCS))

Excess partial molal volume

200/412

2016-04-19 03:35:30

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

butan-1-ol

Sharma; Singh, Jaibir; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 38; nb. 1; (1999); p. 65 - 69, View in Reaxys 34 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

benzene

Yadava, Raja R.; Singh, Vishwanath; Yadava, Sarvanand S.; Journal of Chemical & Engineering Data; vol. 39; nb. 4; (1994); p. 705 - 707, View in Reaxys 35 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

para-xylene

Yadava, Raja R.; Singh, Vishwanath; Yadava, Sarvanand S.; Journal of Chemical & Engineering Data; vol. 39; nb. 4; (1994); p. 705 - 707, View in Reaxys 36 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

mesitylene

Yadava, Raja R.; Singh, Vishwanath; Yadava, Sarvanand S.; Journal of Chemical & Engineering Data; vol. 39; nb. 4; (1994); p. 705 - 707, View in Reaxys 37 of 58

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

methyl cyclohexane

Cordray, James H.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 32; nb. 1; (1987); p. 83 - 85, View in Reaxys 38 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

201/412

2016-04-19 03:35:30

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

tetrachloromethane

Aminabhavi, T. M.; Manjeshwar, L. S.; Balundgi, R. H.; Muddapur, M. V.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical; vol. 26; nb. 2; (1987); p. 106 - 109, View in Reaxys 39 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

dimethyl sulfoxide

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

1-Octanol

Dewan, R. K.; Mehta, S. K.; Journal of Chemical Thermodynamics; vol. 18; nb. 2; (1986); p. 101 - 106, View in Reaxys 41 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

ethylbenzene

Dewan, R. K.; Mehta, S. K.; Journal of Chemical Thermodynamics; vol. 18; nb. 11; (1986); p. 1015 - 1020, View in Reaxys 42 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

25 - 45

Partner (Mechanical & Physical Properties (MCS))

cyclohexane

Marsh, Kenneth N.; Journal of Chemical Thermodynamics; vol. 17; nb. 1; (1985); p. 29 - 42, View in Reaxys 43 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

202/412

2016-04-19 03:35:30

Partner (Mechanical & Physical Properties (MCS))

hexane

Marsh, Kenneth N.; Journal of Chemical Thermodynamics; vol. 17; nb. 1; (1985); p. 29 - 42, View in Reaxys 44 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

25 - 45

Partner (Mechanical & Physical Properties (MCS))

tetrachloromethane

Marsh, Kenneth N.; Journal of Chemical Thermodynamics; vol. 17; nb. 1; (1985); p. 29 - 42, View in Reaxys 45 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

para-xylene

Marsh, Kenneth N.; Journal of Chemical Thermodynamics; vol. 17; nb. 1; (1985); p. 29 - 42, View in Reaxys 46 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

25 - 45

Partner (Mechanical & Physical Properties (MCS))

benzene

Marsh, Kenneth N.; Journal of Chemical Thermodynamics; vol. 17; nb. 1; (1985); p. 29 - 42, View in Reaxys 47 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

30 - 40

Partner (Mechanical & Physical Properties (MCS))

benzene

Nigam, Ram K.; Singh, Prem P.; Mishra, Ruchi; Singh, Mohan; Canadian Journal of Chemistry; vol. 58; (1980); p. 1468 - 1472, View in Reaxys 48 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

30 - 40

Partner (Mechanical & Physical Properties (MCS))

toluene

Nigam, Ram K.; Singh, Prem P.; Mishra, Ruchi; Singh, Mohan; Canadian Journal of Chemistry; vol. 58; (1980); p. 1468 - 1472, View in Reaxys

203/412

2016-04-19 03:35:30

49 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

30 - 40

Partner (Mechanical & Physical Properties (MCS))

o-xylene

Nigam, Ram K.; Singh, Prem P.; Mishra, Ruchi; Singh, Mohan; Canadian Journal of Chemistry; vol. 58; (1980); p. 1468 - 1472, View in Reaxys 50 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

30 - 40

Partner (Mechanical & Physical Properties (MCS))

m-xylene

Nigam, Ram K.; Singh, Prem P.; Mishra, Ruchi; Singh, Mohan; Canadian Journal of Chemistry; vol. 58; (1980); p. 1468 - 1472, View in Reaxys 51 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

30 - 40

Partner (Mechanical & Physical Properties (MCS))

para-xylene

Nigam, Ram K.; Singh, Prem P.; Mishra, Ruchi; Singh, Mohan; Canadian Journal of Chemistry; vol. 58; (1980); p. 1468 - 1472, View in Reaxys 52 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Brown; Smith; Australian Journal of Chemistry; vol. 15; (1962); p. 1,3, View in Reaxys; Nigam et al.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 18; (1979); p. 492, View in Reaxys; Nakanishi; Shirai; Bulletin of the Chemical Society of Japan; vol. 43; (1970); p. 1634,1636, View in Reaxys 53 of 58

Description (Mechanical & Physical Properties (MCS))

PVT Relationship

Wyrzykowska-Stankiewicz; Zieborak; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 8; (1960); p. 655,657, View in Reaxys; Deiters; Schneider; Berichte der Bunsen-Gesellschaft; vol. 80; (1976); p. 1316,1318, View in Reaxys 54 of 58

Description (Mechanical & Physical Properties (MCS))

Adiabatic compressibility

Kaulgud; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 36; (1963); p. 365,372, 373, View in Reaxys 55 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Partner (Mechanical & Physical Properties (MCS))

Benzyl acetate

Moore; Styan; Transactions of the Faraday Society; vol. 52; (1956); p. 1556,1559, View in Reaxys

204/412

2016-04-19 03:35:30

56 of 58

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

water

Smith; Blankenship; Pr.Oklahoma Acad.Sci.; vol. 28; (1948); p. 78; Chem.Abstr.; (1949); p. 2500, View in Reaxys 57 of 58

Description (Mechanical & Physical Properties (MCS))

Virial coefficients

Comment (Mechanical & Physical Properties (MCS))

zweiter Virialkoeffizient.

Pitzer; Gwinn; Journal of the American Chemical Society; vol. 63; (1941); p. 3313, View in Reaxys 58 of 58

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Partner (Mechanical & Physical Properties (MCS))

Glutaronitrile

Phibbs; Journal of Physical Chemistry; vol. 59; (1935); p. 346,349, View in Reaxys Mechanical Properties (9) Description (MeComment (Mechanical Properchanical Properties) ties) Virial coefficients of the equation of state

neat liquid

References

Winey; Duvall; Knudson; Gupta; Journal of Chemical Physics; vol. 113; nb. 17; (2000); p. 7492 - 7501, View in Reaxys

Molar volume

Rohrschneider; Analytical Chemistry; vol. 45; (1973); p. 1241,1242, View in Reaxys; Parcher; Westlake; Journal of Physical Chemistry; vol. 81; (1977); p. 307,308,309,311, View in Reaxys; Mayer; Monatshefte fuer Chemie; vol. 110; (1979); p. 191,195, View in Reaxys; Dewan, R.K.; Sharma, A.K.; Mehta, S.K.; Journal of Solution Chemistry; vol. 17; nb. 5; (1988); p. 459 - 466, View in Reaxys; Yarger, F. L.; Olinger, Bart; Journal of Chemical Physics; vol. 85; nb. 3; (1986); p. 1534 - 1538, View in Reaxys; Ponomarenko, S. M.; Mushtakova, S. P.; Demakhin, A. G.; Faifel', B. L.; Kal'manovich, D. G.; Russian Journal of General Chemistry; vol. 65; nb. 2.1; (1995); p. 160 - 167; Zhurnal Obshchei Khimii; vol. 65; nb. 2; (1995); p. 190 - 198, View in Reaxys

PVT Relationship

Gupta; Hanks; Thermochimica Acta; vol. 21; (1977); p. 143,148,150,151, View in Reaxys; Courtecuisse, Stephane; Cansell, Francois; Fabre, Denise; Petitet, Jean-Pierre; Journal of Chemical Physics; vol. 102; nb. 2; (1995); p. 968 - 974, View in Reaxys

Specific volume

Miller, P. J.; Block, S.; Piermarini, G. J.; Journal of Physical Chemistry; vol. 93; nb. 1; (1989); p. 462 - 466, View in Reaxys; Ponomarenko, S. M.; Mushtakova, S. P.; Demakhin, A. G.; Faifel', B. L.; Kal'manovich, D. G.; Russian Journal of General Chemistry; vol. 65; nb. 2.1; (1995); p. 160 - 167; Zhurnal Obshchei Khimii; vol. 65; nb. 2; (1995); p. 190 - 198, View in Reaxys

Virial coefficients of the equation of state

Vigdergauz; Semkin; Russian Journal of Physical Chemistry; vol. 45; (1971); p. 518,519; ; p. 931, View in Reaxys; Bottomley; Spurling; Australian Journal of Chemistry; vol. 16; (1963); p. 1, View in Reaxys; Bottomley et al.; Journal of the Chemical Society; (1961); p. 2247, View in Reaxys; Lysne; Hardesty; Journal of Chemical Physics; vol. 59; (1973); p. 6512, View in Reaxys; Marsh et al.; Journal of Chemical Thermodynamics; vol. 11; (1979); p. 897,899 - 901, View in Reaxys

Compressibility

Gerger et al.; Monatshefte fuer Chemie; vol. 108; (1977); p. 417,419, View in Reaxys; Rabinowitsch; Zhurnal Fizicheskoi Khimii; vol. 34; (1960); p. 423,424,425; engl.Ausg.; p. 198, View in Reaxys; Derrick; Clever; Journal of Physical Chemistry; vol. 75; (1971); p. 3728, View in Reaxys

205/412

2016-04-19 03:35:30

Viscosity

Gutmann; Schmid; Monatshefte fuer Chemie; vol. 100; (1969); p. 2113,2118, View in Reaxys; Heubel et al.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 15; (1977); p. 687, View in Reaxys; Kotisek; Marek; Chemicky Prumysl; vol. 5; (1955); p. 330,331, 332; Chem.Abstr.; nb. 6239; (1960), View in Reaxys; Golovanov et al.; Russian Journal of Inorganic Chemistry (Translation of Zhurnal Neorganicheskoi Khimii); vol. 17; (1972); p. 578, View in Reaxys; Tommasini et al.; Physica (Amsterdam); vol. 49; (1970); p. 299,311,316,320,321,323, View in Reaxys; Matrosov et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 25; (1976); p. 295,298; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 25; (1976); p. 313, View in Reaxys; Honda; Sasada; Japanese Journal of Applied Physics; vol. 16; (1977); p. 1775,1776-1778, View in Reaxys; Chandra; Nath; Bulletin of the Chemical Society of Japan; vol. 43; (1970); p. 1614, View in Reaxys; Schiavo; Marrosu; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 105; (1977); p. 157,162, 164, 166, View in Reaxys

Virial coefficients of the equation of state

zweiter.

Douslin; Waddington; Journal of Chemical Physics; vol. 23; (1955); p. 2453, View in Reaxys; McCullough et al.; Journal of the American Chemical Society; vol. 76; (1954); p. 4791,4793,4794, View in Reaxys

Internal pressure

Binnendruck.

Molecular Deformation (3) Description (MoComment (Molec- References lecular Deforma- ular Deformation) tion) Fundamental vibrations

Varsanyi et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 23; (1967); p. 1205,1210, View in Reaxys; Singh; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 23; (1967); p. 439,444, View in Reaxys; Yuan, W.; Rabinovitch, B. S.; Tosa, R.; Journal of Physical Chemistry; vol. 86; nb. 14; (1982); p. 2796 - 2799, View in Reaxys; Chen, Sheah; Tolbert, William A.; Dlott, Dana D.; Journal of Physical Chemistry; vol. 98; nb. 32; (1994); p. 7759 - 7766, View in Reaxys; Chen, Sheah; Hong, Xiaoyu; Hill, Jeffrey R.; Dlott, Dana D.; Journal of Physical Chemistry; vol. 99; nb. 13; (1995); p. 4525 - 4530, View in Reaxys

Force constants

Melander; Bergmann; Acta Chemica Scandinavica, Series A: Physical and Inorganic Chemistry; vol. 30; (1976); p. 703, View in Reaxys; Ladd; Orville-Thomas; Spectrochimica Acta; vol. 22; (1966); p. 919,920, View in Reaxys; Verdermame et al.; Journal of Chemical Physics; vol. 56; (1972); p. 2638, View in Reaxys; Marciniak et al.; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 27; (1979); p. 853,854,857, View in Reaxys; Popov; Shlyapochnikov; Optics and Spectroscopy; vol. 15; (1963); p. 174; ; p. 325, View in Reaxys; Miller, P. J.; Block, S.; Piermarini, G. J.; Journal of Physical Chemistry; vol. 93; nb. 1; (1989); p. 462 - 466, View in Reaxys

Fundamental vibrations Optics (13) Description (Optics)

des Molekuels.

Smith et al.; Journal of Chemical Physics; vol. 18; (1950); p. 706,707,712, View in Reaxys

Comment (Optics)

References

Rayleigh scattering

Malmberg; Lippincott; Journal of Colloid and Interface Science; vol. 27; (1968); p. 591,598,606, View in Reaxys; Sazonov; Journal of Structural Chemistry; vol. 14; (1973); p. 507; ; p. 554, View in Reaxys; Sazonov; Zhilyaeva; Russian Journal of Physical Chemistry; vol. 48; (1974); p. 402; ; p. 704, View in Reaxys; Derrick; Clever; Journal of Physical Chemistry; vol. 75; (1971); p. 3728, View in Reaxys; Sassi, Paola; Paliani, Giulio; Cataliotti, Rosario Sergio; Zeitschrift fur Physikalische Chemie; vol. 204; nb. 1-2; (1998); p. 235 - 245, View in Reaxys

Electric birefringence (Kerr effect)

Leiser; Abh.Dtsch.Bunsen-Ges.; nb. 4; p. 69; Chem. Zentralbl.; vol. 82; nb. I; (1911); p. 622, View in Reaxys; Okabayashi; Bulletin of the Chemical Society of Japan; vol. 34; (1961); p. 1010,1012, View in Reaxys; Lutskii et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 43; (1973); p. 2597,2578,2579, View in Reaxys; Ramshaw et al.; Journal of Chemical Physics; vol. 54; (1971); p. 1239,1244, View in Reaxys; Lutskii et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 43; (1973); p. 2462,2449, View in Reaxys; Burnham et al.; Journal of Chemical Physics; vol. 67; (1977); p. 4990, View in Reaxys; Ivanov, N. I.; Prezhdo, O. V.; Tarasova, G. V.; Akulova, O. N.; Prezhdo, V. V.; Tyurin, S. A.; Russian Journal of Physical Chemistry; vol. 68; nb. 5; (1994); p. 821 - 827; Zhurnal Fizicheskoi Khimii; vol. 68; nb. 5; (1994); p. 912 - 918, View in Reaxys; Giorgini, M. G.; Foggi, P.;

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Cataliotti, R. S.; Distefano, M. R.; Moressi, A.; Mariani, L.; Journal of Chemical Physics; vol. 102; nb. 22; (1995); p. 8763 - 8772, View in Reaxys Degree of depolarization of Rayleigh scattering

Giorgini, M. G.; Foggi, P.; Cataliotti, R. S.; Distefano, M. R.; Moressi, A.; Mariani, L.; Journal of Chemical Physics; vol. 102; nb. 22; (1995); p. 8763 - 8772, View in Reaxys

Magnetic birefringence (CottonMouton effect)

Cotton; Mouton; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 154; (1912); p. 930; Annales de Chimie (Cachan, France); vol. <8>28; (1913); p. 236, View in Reaxys; Le Fevre et al.; Australian Journal of Chemistry; vol. 24; (1971); p. 1177,1180, View in Reaxys; Vul'fson, S. G.; Nikolaev, V. F.; Timosheva, A. P.; Vereshchagin, A. N.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 34; nb. 11; (1985); p. 2307 - 2311; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 11; (1985); p. 2495 - 2499, View in Reaxys

Magnetic circular dichroism

Barth et al.; Journal of the Chemical Society, Chemical Communications; (1975); p. 672, View in Reaxys; Barth et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1979); p. 907,908, View in Reaxys

Reflection

Ascarelli; Chemical Physics Letters; vol. 39; (1976); p. 23, View in Reaxys

Optical properties

Yakusheva et al.; High Temperatures - High Pressures; vol. 3; (1971); p. 261,262-266, View in Reaxys

Magnetorotation

Bonnafous; Labarre; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 66; (1969); p. 1376, View in Reaxys

Diffraction

Vincent-Geisse; Journal de Physique (Paris); vol. 26; (1965); p. 289,292, View in Reaxys

Degree of depola- DepolarisationsLe Fevre; Rao; Journal of the Chemical Society; (1958); p. 1465, View in Reaxys rization of Raygrad des in Gemileigh scattering schen mit Tetrachlormethan gestreuten Lichts. Electric birefringence (Kerr effect)

Kerr-Konstante.

Le Fevre; Le Fevre; Journal of the Chemical Society; (1954); p. 1577,1581; Australian Journal of Chemistry; vol. 7; (1954); p. 33,35, View in Reaxys

Diffraction

Elektronenbeugung des Dampfes.

Degard; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 202; (1936); p. 1278, View in Reaxys; Brockway; Beach; Pauling; Journal of the American Chemical Society; vol. 57; (1935); p. 2703, View in Reaxys; Rogowski; Chemische Berichte; vol. 75; (1942); p. 244,257,262, View in Reaxys

Magnetorotation

Magnetische Rotation.

Perkin; Journal of the Chemical Society; vol. 55; (1889); p. 748, View in Reaxys

Other Thermochemical Data (12) Description (Oth- Comment (Other er Thermochemi- Thermochemical cal Data) Data)

References

Entropy

Pitzer; Gwinn; Journal of the American Chemical Society; vol. 63; (1941); p. 3313, View in Reaxys; Jones; Giauque; Journal of the American Chemical Society; vol. 69; (1947); p. 984, View in Reaxys; Goffredi, Mario; Liszi, Janos; Nemeth, Bela; Liveri, Vincenzo Turco; Journal of Solution Chemistry; vol. 12; nb. 4; (1983); p. 221 - 232, View in Reaxys; Langlet, J.; Claverie, P.; Caillet, J.; Pullman, A.; Journal of Physical Chemistry; vol. 92; nb. 6; (1988); p. 1617 - 1631, View in Reaxys

Thermodynamic properties

Cox; Parker; Journal of the American Chemical Society; vol. 95; (1973); p. 402,403-407, View in Reaxys; Cox et al.; Journal of the American Chemical Society; vol. 95; (1973); p. 1010, View in Reaxys; DeMaine; Journal of Molecular Spectroscopy; vol. 4; (1960); p. 407,408, View in Reaxys; Gilbert; Treuwith; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1973); p. 2010,2013, View in Reaxys; Franklin; Sharma; Journal of Chemical Physics; vol. 58; (1973); p. 409, View in Reaxys; Belik et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 25; (1976); p. 1619,1620,1621; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 25; (1976); p. 1714, View in Reaxys; Liszi; Acta Chimica Academiae Scientiarum Hungaricae; vol. 98; (1978); p. 93,95, View in Reaxys; Cumming; Kebarle; Journal of the American Chemical Society; vol. 100; (1978); p. 1835,1836, View in Reaxys; Czworniak et al.; Chemical Physics; vol. 11; (1975); p. 451,466,469, View in Reaxys; Mayer; Monatshefte fuer Chemie; vol. 110; (1979); p. 191,195, View in Reaxys; Wilhelm; Battino; Journal of Chemical Physics; vol.

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55; (1971); p. 4012,4014, View in Reaxys; Mayer; Monatshefte fuer Chemie; vol. 109; (1978); p. 775,776,778,780,782-785, View in Reaxys Enthalpy

Pivina et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 24; (1975); p. 59,60,61; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 24; (1975); p. 68, View in Reaxys; Pivina et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 26; (1977); p. 158; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 26; (1977); p. 182, View in Reaxys; Belik; Shlyapochnikov; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 26; (1977); p. 2585; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 26; (1977); p. 2795, View in Reaxys

Heat of combustion at constant volume

Knobel et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 20; (1971); p. 425,426,427; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 20; (1971); p. 485, View in Reaxys

Heat capacity

Berman; West; Journal of Chemical and Engineering Data; vol. 14; (1969); p. 107, View in Reaxys

Cryoscopic constant

Ljaschkewitsch; Neftekhimiya; vol. 1; (1961); p. 329,329,332, View in Reaxys

Heat of combustion at constant volume

bei 26.7grad: 174.4 kcal/Mol.

Cass et al.; Journal of the Chemical Society; (1958); p. 958,960, View in Reaxys

Heat of combustion at constant volume

bei 25grad:175.25 Holcomb; Dorsey; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2788, kcal/Mol. View in Reaxys

Ebullioscopic con- 1.86 (fuer 1000 g stant Loesungsmittel).

Philip; Waterton; Journal of the Chemical Society; (1930); p. 2783, View in Reaxys

Heat of combustion at constant volume

in fluess. Zustand:169.95 kcal/Mol.

Swientoslawski; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 72; (1910); p. 66; Chem. Zentralbl.; vol. 80; nb. II; (1909); p. 2144, View in Reaxys

Cryoscopic constant

Molakulare Siede- Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftpunktserhoehung: slehre; vol. 55; (1906); p. 291, View in Reaxys 19.5.

Heat of combustion at constant volume

in Dampf:170.25 kcal/Mol.

Berthelot; Matignon; Annales de Chimie (Cachan, France); vol. <6> 30; (1893); p. 557, View in Reaxys

Partition octan-1-ol/water (MCS) (1) 1 of 1

log POW

-0.284

Smith; Perfetti; Garg; Hansch; Food and Chemical Toxicology; vol. 41; nb. 6; (2003); p. 807 - 817, View in Reaxys Self-diffusion (2) Comment (SelfReferences diffusion) O'Reilly; Journal of Chemical Physics; vol. 55; (1971); p. 2876,2877, View in Reaxys; O'Reilly; Peterson; Journal of Chemical Physics; vol. 55; (1971); p. 2155,2159, View in Reaxys SelbstdiffusionMcCall et al.; Journal of Chemical Physics; vol. 31; (1959); p. 1555, View in Reaxys skoeffizient:Temperaturabhaengigkeit und Druckabhaengigkeit des Selbsdiffusionskoeffizienten. Solubility (MCS) (12) 1 of 12

Saturation

in pure solvent

Comment (Solubility (MCS))

equation

Jain, Neera; Yalkowsky, Samuel H.; Journal of Pharmaceutical Sciences; vol. 90; nb. 2; (2001); p. 234 - 252, View in Reaxys 2 of 12

Saturation

in pure solvent

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Kamlet, Mortimer J.; Doherty, Ruth M.; Abraham, Michael H.; Carr, Peter W.; Doherty, Robert F.; Taft, Robert W.; Journal of Physical Chemistry; vol. 91; nb. 7; (1987); p. 1996 - 2004, View in Reaxys; Valvani; Yalkowsky; Roseman; Journal of Pharmaceutical Sciences; vol. 70; nb. 5; (1981); p. 502 - 507, View in Reaxys; Kamlet; Doherty; Abboud; Abraham; Taft; Journal of Pharmaceutical Sciences; vol. 75; nb. 4; (1986); p. 338 - 349, View in Reaxys 3 of 12

Comment (Solubility (MCS))

In Isopren

Boublikova; Collection of Czechoslovak Chemical Communications; vol. 38; (1973); p. 2033, View in Reaxys 4 of 12

Comment (Solubility (MCS))

In 2-Methylbuten

Boublikova; Collection of Czechoslovak Chemical Communications; vol. 38; (1973); p. 2033, View in Reaxys 5 of 12

Comment (Solubility (MCS))

in Pentadecafluorheptan

Konecny; Deal; Journal of Physical Chemistry; vol. 67; (1963); p. 504,505, View in Reaxys 6 of 12

Comment (Solubility (MCS))

im System mit Ethanol und Ethylenglykol bei 28 und 40grad

Markusin; Nikanorowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 32; (1962); p. 3469,3407, View in Reaxys 7 of 12

Comment (Solubility (MCS))

in Heptan, Octan, Nonan bei verschied. Temp.

Malesinska; Malesinski; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 8; (1960); p. 61,64, View in Reaxys 8 of 12

Solvent (Solubility (MCS))

H2O; D2O

Comment (Solubility (MCS))

at:20-103 degreeC.

Rabinowitsch et al.; Doklady Akademii Nauk SSSR; vol. 105; (1955); p. 108,109; Chem. Zentralbl.; vol. 127; (1956); p. 9845, View in Reaxys 9 of 12

Temperature (Solubility (MCS)) [°C]

26.7

Solvent (Solubility (MCS))

H2O; acetic acid

Skrzec; Murphy; Industrial and Engineering Chemistry; vol. 46; (1954); p. 2245, View in Reaxys 10 of 12

Temperature (Solubility (MCS)) [°C]

0.7

Solvent (Solubility (MCS))

H2O

Comment (Solubility (MCS))

100 g solvent dissolves. 9.32 g Substance.

Macy; Gehauf; Science (Washington, DC, United States); vol. 106; p. 274; Chem.Abstr.; (1947); p. 7206, View in Reaxys 11 of 12

Temperature (Solubility (MCS)) [°C]

40.5

Solvent (Solubility (MCS))

H2O

Comment (Solubility (MCS))

100 g solvent dissolves. 13.17 g Substance.

Macy; Gehauf; Science (Washington, DC, United States); vol. 106; p. 274; Chem.Abstr.; (1947); p. 7206, View in Reaxys 12 of 12

Temperature (Solubility (MCS)) [°C]

Solvent (Solubility (MCS))

H2O

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Comment (Solubility (MCS))

Solubility :11.03 percent.

Schumacher; Hunt; Industrial and Engineering Chemistry; vol. 34; (1942); p. 703, View in Reaxys; Wright; MurrayRust; Hartley; Journal of the Chemical Society; (1931); p. 202, View in Reaxys Solution Behaviour (MCS) (46) 1 of 46

Description (Solution Behaviour (MCS))

Miscibility

Temperature (Solution Behaviour (MCS)) [°C]

29.52 - 39.9

Partner (Solution Behaviour (MCS))

ethylene glycol

Milewska; Siporska; Szydlowski; Polish Journal of Chemistry; vol. 78; nb. 4; (2004); p. 591 - 594, View in Reaxys 2 of 46

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

10.3 - 28.8

Partner (Solution Behaviour (MCS))

1-octanoic acid; glycerol

Sazonov, Valerii P.; Sazonov, Nikolai V.; Lisov, Nikolai I.; Journal of Chemical and Engineering Data; vol. 47; nb. 6; (2002); p. 1462 - 1465, View in Reaxys 3 of 46

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

11.2 - 31.5

Partner (Solution Behaviour (MCS))

hexan-1-ol; glycerol

Sazonov, Valerii P.; Sazonov, Nikolai V.; Lisov, Nikolai I.; Journal of Chemical and Engineering Data; vol. 47; nb. 6; (2002); p. 1462 - 1465, View in Reaxys 4 of 46

Description (Solution Behaviour (MCS))

Miscibility

Temperature (Solution Behaviour (MCS)) [°C]

24.13 - 27.97

Partner (Solution Behaviour (MCS))

n-pentan-1-ol

Szydlowski; Milewska; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 505 - 508, View in Reaxys 5 of 46

Description (Solution Behaviour (MCS))

Miscibility

Temperature (Solution Behaviour (MCS)) [°C]

25.77 - 28.12

Partner (Solution Behaviour (MCS))

1-pentanol-d1

Szydlowski; Milewska; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 505 - 508, View in Reaxys 6 of 46

Description (Solution Behaviour (MCS))

Miscibility

Temperature (Solution Behaviour (MCS)) [°C]

16.22 - 18.38

Partner (Solution Behaviour (MCS))

i-Butyl alcohol

Szydlowski; Milewska; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 505 - 508, View in Reaxys

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7 of 46

Description (Solution Behaviour (MCS))

Miscibility

Temperature (Solution Behaviour (MCS)) [°C]

15.96 - 18.52

Partner (Solution Behaviour (MCS))

iso-BuOD

Szydlowski; Milewska; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 505 - 508, View in Reaxys 8 of 46

Description (Solution Behaviour (MCS))

Solubility [Henry constant]

Temperature (Solution Behaviour (MCS)) [°C]

20 - 50

Partner (Solution Behaviour (MCS))

H2O

Dohnal; Benes; Journal of Chemical and Engineering Data; vol. 44; nb. 5; (1999); p. 1097 - 1102, View in Reaxys 9 of 46

Description (Solution Behaviour (MCS))

Solubility [Ostwald absorption coefficient]

Temperature (Solution Behaviour (MCS)) [°C]

24.85

Partner (Solution Behaviour (MCS))

methanol

Abraham, Michael H.; Whiting, Gary S.; Carr, Peter W.; Ouyang, Hsiu; Journal of the Chemical Society. Perkin Transactions 2; nb. 6; (1998); p. 1385 - 1390, View in Reaxys 10 of 46

Description (Solution Behaviour (MCS))

Mutual solubility

Partner (Solution Behaviour (MCS))

hexane

Zenkevich; Tsibul'skaya; Russian Journal of Physical Chemistry A; vol. 71; nb. 2; (1997); p. 281 - 286, View in Reaxys 11 of 46

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

0 - 89.8

Partner (Solution Behaviour (MCS))

H2O

Stephenson; Journal of Chemical and Engineering Data; vol. 37; nb. 1; (1992); p. 80 - 95, View in Reaxys 12 of 46

Description (Solution Behaviour (MCS))

Miscibility

Partner (Solution Behaviour (MCS))

ethylene glycol

Salvi, Madhuri V.; Hook, W. Alexander Van; Journal of Physical Chemistry; vol. 94; nb. 20; (1990); p. 7812 - 7820, View in Reaxys 13 of 46

Description (Solution Behaviour (MCS))

Miscibility

Partner (Solution Behaviour (MCS))

lt;O,O'-(2)H2gt;-ethylene glycol

Salvi, Madhuri V.; Hook, W. Alexander Van; Journal of Physical Chemistry; vol. 94; nb. 20; (1990); p. 7812 - 7820, View in Reaxys 14 of 46

Description (Solution Behaviour (MCS))

Mutual solubility

Partner (Solution Behaviour (MCS))

water

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Sazonov, V. P.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 11.1; (1989); p. 2431 - 2435,2173 - 2176, View in Reaxys 15 of 46

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

40.1 - 108.4

Partner (Solution Behaviour (MCS))

n-heptane

Sazonov, V. P.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 11.1; (1989); p. 2431 - 2435,2173 - 2176, View in Reaxys 16 of 46

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

15.1 - 42.9

Partner (Solution Behaviour (MCS))

1-heptanol

Sazonov, V. P.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 11.1; (1989); p. 2431 - 2435,2173 - 2176, View in Reaxys 17 of 46

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

25.1 - 59.8

Partner (Solution Behaviour (MCS))

1-Decanol

Sazonov, V. P.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 11.1; (1989); p. 2431 - 2435,2173 - 2176, View in Reaxys 18 of 46

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

-40 - 56.6

Partner (Solution Behaviour (MCS))

ethylene glycol; 1,1,2,2-tetrachloroethylene

Sazonov, V. P.; J. Appl. Chem. USSR (Engl. Transl.); vol. 59; nb. 1; (1986); p. 12 - 18,10 - 15, View in Reaxys 19 of 46

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

Partner (Solution Behaviour (MCS))

isopropyl alcohol; H2O

Sazonov; Journal of applied chemistry of the USSR; vol. 59; nb. 7 pt 1; (1986); p. 1348 - 1352, View in Reaxys 20 of 46

Description (Solution Behaviour (MCS))

Solubilizing

Partner (Solution Behaviour (MCS))

Makitra, R. G.; Pirig, Ya. N.; Politanskaya, T. I.; J. Appl. Chem. USSR (Engl. Transl.); vol. 54; nb. 1; (1981); p. 54 58,47 - 51, View in Reaxys 21 of 46

Description (Solution Behaviour (MCS))

Solubilizing

Partner (Solution Behaviour (MCS))

Makitra, R. G.; Pirig, Ya. N.; Politanskaya, T. I.; J. Appl. Chem. USSR (Engl. Transl.); vol. 54; nb. 1; (1981); p. 54 58,47 - 51, View in Reaxys

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22 of 46

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

20.5

Partner (Solution Behaviour (MCS))

1,2-dichlorobenzene; n-heptane

Patel, Amrit N.; Journal of Chemical & Engineering Data; vol. 26; nb. 2; (1981); p. 124 - 127, View in Reaxys 23 of 46

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

20.5

Partner (Solution Behaviour (MCS))

para-dichlorobenzene; n-heptane

Patel, Amrit N.; Journal of Chemical & Engineering Data; vol. 26; nb. 2; (1981); p. 124 - 127, View in Reaxys 24 of 46

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

31.9 - 156.3

Partner (Solution Behaviour (MCS))

cetane

Rogalski, Marek; Stryjek, Roman; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 28; nb. 2; (1980); p. 139 - 147, View in Reaxys 25 of 46

Description (Solution Behaviour (MCS))

Dissolving capacity

Hangen; Friedman; Journal of Physical Chemistry; vol. 67; (1963); p. 1757,1759, View in Reaxys; Haugen; Friedman; Journal of Physical Chemistry; vol. 72; (1968); p. 4549, View in Reaxys; Guk et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 51; (1978); p. 2602,2480, View in Reaxys; Chaenko et al.; Russian Journal of Physical Chemistry; vol. 53; (1979); p. 1113; ; p. 1989, View in Reaxys; Kedrinskii; Sukhorukova; Russian Journal of Physical Chemistry; vol. 49; (1975); p. 1095; ; p. 1857, View in Reaxys 26 of 46

Description (Solution Behaviour (MCS))

Miscibility

Sazonov; Chernysheva; J. Appl. Chem. USSR (Engl. Transl.); vol. 52; (1979); p. 2717,2572, View in Reaxys; Ferloni et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 26; (1971); p. 1713, View in Reaxys; Pavlova et al.; Russian Journal of Physical Chemistry; vol. 49; (1975); p. 1693; ; p. 2874, View in Reaxys 27 of 46

Description (Solution Behaviour (MCS))

Mutual solubility

Hwa et al.; Journal of Chemical and Engineering Data; vol. 8; (1963); p. 409, View in Reaxys 28 of 46

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

Partner (Solution Behaviour (MCS))

cis-Octadecenoic acid

Pasquinelli; Transactions of the Faraday Society; vol. 53; (1957); p. 932,936, View in Reaxys 29 of 46

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

noble gases

Friedman; Journal of the American Chemical Society; vol. 76; (1954); p. 3294,3295, View in Reaxys 30 of 46

Description (Solution Behaviour (MCS))

Dissolving capacity

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Partner (Solution Behaviour (MCS))

nitrogen

Friedman; Journal of the American Chemical Society; vol. 76; (1954); p. 3294,3295, View in Reaxys 31 of 46

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

sulfur hexafluoride

Friedman; Journal of the American Chemical Society; vol. 76; (1954); p. 3294,3295, View in Reaxys 32 of 46

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

osmium(VIII)-oxide

Friedman; Journal of the American Chemical Society; vol. 76; (1954); p. 3294,3295, View in Reaxys 33 of 46

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

Partner (Solution Behaviour (MCS))

water

v.Schickh; Angewandte Chemie; vol. 62; (1950); p. 547,554, View in Reaxys 34 of 46

Description (Solution Behaviour (MCS))

Dissolving capacity

Comment (Solution Behaviour (MCS))

fuer anorganische Saeuren und Salze.

Garwin; Hixson; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2299, View in Reaxys; Broensted; Delbanco; Volqvartz; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 162; (1932); p. 133, View in Reaxys; Jaffe; Canadian Journal of Research, Section B: Chemical Sciences; vol. 27; (1949); p. 644; Chem.Abstr.; (1950); p. 1305, View in Reaxys; Arlman; Recueil des Travaux Chimiques des Pays-Bas; vol. 56; (1937); p. 921,922, View in Reaxys 35 of 46

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

aluminium trichloride

Schmerling; Industrial and Engineering Chemistry; vol. 40; (1948); p. 2072,2074, View in Reaxys 36 of 46

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

fatty acid

Hoerr; Sedgwick; Ralston; Journal of Organic Chemistry; vol. 11; (1946); p. 603,604, View in Reaxys 37 of 46

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Behaviour (MCS)) [°C]

Comment (Solution Behaviour (MCS))

loesen sich 2.28 Gew-prozent.

Partner (Solution Behaviour (MCS))

water

Schumacher; Hunt; Industrial and Engineering Chemistry; vol. 34; (1942); p. 703, View in Reaxys; Wright; MurrayRust; Hartley; Journal of the Chemical Society; (1931); p. 202, View in Reaxys 38 of 46

Description (Solution Behaviour (MCS))

Miscibility

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Comment (Solution Behaviour (MCS))

Einfluss des Druckes.

Partner (Solution Behaviour (MCS))

tetrachloromethane

Poppe; Bulletin des Societes Chimiques Belges; vol. 44; (1935); p. 644, View in Reaxys 39 of 46

Description (Solution Behaviour (MCS))

Miscibility

Comment (Solution Behaviour (MCS))

Einfluss des Druckes.

Partner (Solution Behaviour (MCS))

CS2

Poppe; Bulletin des Societes Chimiques Belges; vol. 44; (1935); p. 644, View in Reaxys 40 of 46

Description (Solution Behaviour (MCS))

Miscibility

Comment (Solution Behaviour (MCS))

Einfluss des Druckes.

Partner (Solution Behaviour (MCS))

cyclohexane

Poppe; Bulletin des Societes Chimiques Belges; vol. 44; (1935); p. 644, View in Reaxys 41 of 46

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

hydrocarbon

Mulliken; Wakeman; Recueil des Travaux Chimiques des Pays-Bas; vol. 54; (1935); p. 366,369; Industrial and Engineering Chemistry, Analytical Edition; vol. 7; (1935); p. 276, View in Reaxys 42 of 46

Description (Solution Behaviour (MCS))

Mutual solubility

Partner (Solution Behaviour (MCS))

CS2

Joukovsky; Bulletin des Societes Chimiques Belges; vol. 43; (1934); p. 401, View in Reaxys 43 of 46

Description (Solution Behaviour (MCS))

Miscibility

Pressure (Solution Behaviour (MCS)) [Torr]

760 - 114000

Partner (Solution Behaviour (MCS))

water

Timmermans; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 20; (1923); p. 506, View in Reaxys 44 of 46

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

4-nitrobenzyl chloride

v. Halban; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 84; (1913); p. 144, View in Reaxys 45 of 46

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

trimethylamine

v. Halban; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 84; (1913); p. 144, View in Reaxys 46 of 46

Description (Solution Behaviour (MCS))

Dissolving capacity

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Partner (Solution Behaviour (MCS))

triethylamine

v. Halban; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 84; (1913); p. 144, View in Reaxys Sound Properties (9) Description Comment (Sound (Sound ProperProperties) ties) Velocity of sound

temperature dependence

References

Romani; Troncoso; Tovar; Cerdeirina; Carballo; Journal of Chemical and Engineering Data; vol. 46; nb. 2; (2001); p. 312 - 316, View in Reaxys; Makowska, Anna; Szydlowski, Jerzy; Journal of Chemical and Engineering Data; vol. 50; nb. 4; (2005); p. 1365 1369, View in Reaxys

Velocity of sound

Busse; Annalen der Physik (Weinheim, Germany); vol. <4> 75; (1924); p. 662, View in Reaxys; Reese et al.; Journal of Chemical and Engineering Data; vol. 15; (1970); p. 140,141, View in Reaxys; Vitali, Giovanni; Berchiesi, Gianfrancesco; Berchiesi, Maria A.; Gioia Lobbia, Giancarlo; Journal de Chimie Physique et de PhysicoChimie Biologique; vol. 77; nb. 9; (1980); p. 865 - 868, View in Reaxys; Sassi, Paola; Paliani, Giulio; Cataliotti, Rosario Sergio; Zeitschrift fur Physikalische Chemie; vol. 204; nb. 1-2; (1998); p. 235 - 245, View in Reaxys

Sound absorption

Khabibullaev et al.; Moscow University Chemistry Bulletin (English Translation); vol. 27; nb. 3; (1971); p. 66; ; p. 337, View in Reaxys

Acoustic relaxation

Sukhotina; Shakhparonov; Moscow University Chemistry Bulletin (English Translation); vol. 21; (1966); p. 5; ; nb. 1; p. 9, View in Reaxys

Ultrasonic properties

Kaulgud; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 36; (1963); p. 365,372, 373, View in Reaxys

Velocity of sound

Temperaturkoeffizient der Schallgeschwindigkeit.

Willard; J.acoust.Soc.Am.; vol. 19; (1947); p. 235; Chem.Abstr.; (1948); p. 8583, View in Reaxys; Schaaffs; Z.phsik.Chem.; vol. 194; (1944); p. 36,37,77, View in Reaxys

Velocity of sound

in Nitromethan bei 20grad:1346 m/sec.

Schaaffs; Z.phsik.Chem.; vol. 194; (1944); p. 36,37,77, View in Reaxys

Velocity of sound

in Nitromethan bei 23-27grad: 1335 m/sec.

Willard; J.acoust.Soc.Am.; vol. 12; (1941); p. 442; Chem.Abstr.; (1941); p. 5008, View in Reaxys

Velocity of sound

in Nitromethan bei 28grad:1359 m/sec.

Bhimasenachar; Venkateswarlu; Proceedings - Indian Academy of Sciences, Section A; vol. 11; p. 29; Chem.Abstr.; (1940); p. 3553, View in Reaxys

Space Group (1) Space Group 19

References Bagryanskaya, Yu. i.; Gatilov, Yu. V.; Journal of Structural Chemistry; vol. 24; nb. 1; (1983); p. 150 - 151; Zhurnal Strukturnoi Khimii; vol. 24; nb. 1; (1983); p. 158 - 160, View in Reaxys; Trevino, S. F.; Prince, E.; Hubbard, C. R.; Journal of Chemical Physics; vol. 73; nb. 6; (1980); p. 2996 - 3000, View in Reaxys

Static Dielectric Constant (3) Static Dielectric Temperature Constant (Static Dielectric Constant) [°C] 35.8

References

27.75 Surface Tension (14) Surface Tension Temperature [g·s-2] (Surface Tension) [°C]

Grimm; Patrick; Journal of the American Chemical Society; vol. 45; (1923); p. 2799, View in Reaxys References

216/412

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27.33 - 37.36

20 - 80

Korosi; Kovats; Journal of Chemical and Engineering Data; vol. 26; nb. 3; (1981); p. 323 - 332, View in Reaxys Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 65; (1909); p. 134; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 66; (1909); p. 395,427, View in Reaxys; Snead; Clever; Journal of Chemical and Engineering Data; vol. 7; (1962); p. 393, View in Reaxys; Sarkisov; Sazonov; Russian Journal of Physical Chemistry; vol. 44; (1970); p. 1648, View in Reaxys

37.7

Kisel'; Zhurnal Eksperimental'noi i Teoreticheskoi Fiziki; vol. 29; (1955); p. 658,659; Soviet Physics JETP; vol. 2; (1956); p. 520,521, View in Reaxys

35.9

Thompson et al.; Journal of the American Chemical Society; vol. 76; (1954); p. 3445, View in Reaxys

36.7

Thompson et al.; Journal of the American Chemical Society; vol. 76; (1954); p. 3445, View in Reaxys

37.5

Thompson et al.; Journal of the American Chemical Society; vol. 76; (1954); p. 3445, View in Reaxys

30.88 - 37.23

17.3 - 60.9

Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys

35.78

Boyd; Copeland; Journal of the American Chemical Society; vol. 64; (1942); p. 2542, View in Reaxys

35.51

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 558, View in Reaxys

36.98

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 558, View in Reaxys

37.74

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 558, View in Reaxys

36.82

Harkins; Clark; Roberts; Journal of the American Chemical Society; vol. 42; (1920); p. 703, View in Reaxys

25.4 - 40.6

-21.5 - 101.4

Jaeger; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 101; (1917); p. 66, View in Reaxys

0 - 45

Morgan; Stone; Journal of the American Chemical Society; vol. 35; (1913); p. 1517, View in Reaxys

Transition Point(s) of Liquid Modification(s) (2) Temperature Change of Modifi- References (Transition cation Point(s) of Liquid Modification(s)) [°C] -41.15

From crystalline to -

Mohacek Grosev, Vlasta; Stelzer, Franz; Jocham, Daniel; Journal of Molecular Structure; vol. 476; nb. 1-3; (1999); p. 181 - 189, View in Reaxys

-29.15

From - to isotropic Mohacek Grosev, Vlasta; Stelzer, Franz; Jocham, Daniel; Journal of Molecular Structure; vol. 476; nb. 1-3; (1999); p. 181 - 189, View in Reaxys

Transport Data (1) Description References (Transport Data) Thermal conductivity

Vines; Australian Journal of Chemistry; vol. 6; (1953); p. 1,8,10, View in Reaxys; Sakiadis; Coates; A.I.Ch.E.Journal; vol. 1; (1955); p. 275,277, View in Reaxys; Vines; Bennett; Journal of Chemical Physics; vol. 22; (1954); p. 360,362, View in Reaxys; Chu et al.; Journal of Applied Chemistry; vol. 1; (1951); p. 73,79, View in Reaxys; Tommasini et al.; Physica (Amsterdam); vol. 49; (1970); p. 299,311,316,320,321,323, View in Reaxys

Transport Phenomena (MCS) (63) 1 of 63

Description (Transport Phenomena (MCS))

Dynamic viscosity

Comment (Transport Phenomena (MCS))

temperature dependence

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Partner (Transport Phenomena (MCS))

n-pentan-1-ol

Makowska, Anna; Szydlowski, Jerzy; Journal of Chemical and Engineering Data; vol. 50; nb. 4; (2005); p. 1365 1369, View in Reaxys 2 of 63

Description (Transport Phenomena (MCS))

Dynamic viscosity

Comment (Transport Phenomena (MCS))

temperature dependence

Partner (Transport Phenomena (MCS))

1-pentanol-d1

Makowska, Anna; Szydlowski, Jerzy; Journal of Chemical and Engineering Data; vol. 50; nb. 4; (2005); p. 1365 1369, View in Reaxys 3 of 63

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

concentration dependence

Partner (Transport Phenomena (MCS))

methanol

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 4 of 63

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

concentration dependence

Partner (Transport Phenomena (MCS))

ethanol

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 5 of 63

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

concentration dependence

Partner (Transport Phenomena (MCS))

propan-1-ol

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 6 of 63

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

concentration dependence

Partner (Transport Phenomena (MCS))

isopropyl alcohol

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys

218/412

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7 of 63

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

concentration dependence

Partner (Transport Phenomena (MCS))

butan-1-ol

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 8 of 63

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

concentration dependence

Partner (Transport Phenomena (MCS))

i-Butyl alcohol

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 9 of 63

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

concentration dependence

Partner (Transport Phenomena (MCS))

acetone

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 10 of 63

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

concentration dependence

Partner (Transport Phenomena (MCS))

butanone

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 11 of 63

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

concentration dependence

Partner (Transport Phenomena (MCS))

acetic acid methyl ester

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 12 of 63

Description (Transport Phenomena (MCS))

Dynamic viscosity

219/412

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Temperature (Transport 25 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

concentration dependence

Partner (Transport Phenomena (MCS))

ethyl acetate

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 13 of 63

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

concentration dependence

Partner (Transport Phenomena (MCS))

tetrachloromethane

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 14 of 63

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

concentration dependence

Partner (Transport Phenomena (MCS))

benzene

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 15 of 63

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

concentration dependence

Partner (Transport Phenomena (MCS))

toluene

Agarwal, Dimple; Singh, Mukhtar; Journal of the Indian Chemical Society; vol. 81; nb. 10; (2004); p. 850 - 859, View in Reaxys 16 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 - 40 Phenomena (MCS)) [°C] Pressure (Transport Phenomena (MCS)) [Torr]

760

Partner (Transport Phenomena (MCS))

methanol

Tu; Lee; Peng; Journal of Chemical and Engineering Data; vol. 46; nb. 1; (2001); p. 151 - 155, View in Reaxys 17 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 - 40 Phenomena (MCS)) [°C]

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Pressure (Transport Phenomena (MCS)) [Torr]

760

Partner (Transport Phenomena (MCS))

ethanol

Tu; Lee; Peng; Journal of Chemical and Engineering Data; vol. 46; nb. 1; (2001); p. 151 - 155, View in Reaxys 18 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 - 40 Phenomena (MCS)) [°C] Pressure (Transport Phenomena (MCS)) [Torr]

760

Partner (Transport Phenomena (MCS))

propan-1-ol

Tu; Lee; Peng; Journal of Chemical and Engineering Data; vol. 46; nb. 1; (2001); p. 151 - 155, View in Reaxys 19 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 - 40 Phenomena (MCS)) [°C] Pressure (Transport Phenomena (MCS)) [Torr]

760

Partner (Transport Phenomena (MCS))

isopropyl alcohol

Tu; Lee; Peng; Journal of Chemical and Engineering Data; vol. 46; nb. 1; (2001); p. 151 - 155, View in Reaxys 20 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 - 40 Phenomena (MCS)) [°C] Pressure (Transport Phenomena (MCS)) [Torr]

760

Partner (Transport Phenomena (MCS))

iso-butanol

Tu; Lee; Peng; Journal of Chemical and Engineering Data; vol. 46; nb. 1; (2001); p. 151 - 155, View in Reaxys 21 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 - 40 Phenomena (MCS)) [°C] Pressure (Transport Phenomena (MCS)) [Torr]

760

Partner (Transport Phenomena (MCS))

tert-butanol

Tu; Lee; Peng; Journal of Chemical and Engineering Data; vol. 46; nb. 1; (2001); p. 151 - 155, View in Reaxys 22 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 - 40 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

acetic acid methyl ester

Lee; Tu; Journal of Chemical and Engineering Data; vol. 44; nb. 1; (1999); p. 108 - 111, View in Reaxys

221/412

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23 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 - 40 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

ethyl acetate

Lee; Tu; Journal of Chemical and Engineering Data; vol. 44; nb. 1; (1999); p. 108 - 111, View in Reaxys 24 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 - 40 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

1-Propyl acetate

Lee; Tu; Journal of Chemical and Engineering Data; vol. 44; nb. 1; (1999); p. 108 - 111, View in Reaxys 25 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 - 40 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

acetic acid butyl ester

Lee; Tu; Journal of Chemical and Engineering Data; vol. 44; nb. 1; (1999); p. 108 - 111, View in Reaxys 26 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 5 - 45 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

acetonitrile

D'Aprano, A.; Capalbi, A.; Iammarino, M.; Mauro, V.; Princi, A.; Sesta, B.; Journal of Solution Chemistry; vol. 24; nb. 3; (1995); p. 227 - 240, View in Reaxys 27 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

1,1,1- trichloroethane

Lorenzi, Lorenzo De; Fermeglia, Maurizio; Torriano, Giovanni; Journal of Chemical & Engineering Data; vol. 40; nb. 6; (1995); p. 1172 - 1177, View in Reaxys 28 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

propylene Carbonate

Wawrzyniak, G.; Warnke, Z.; Polish Journal of Chemistry; vol. 68; nb. 4; (1994); p. 817 - 824, View in Reaxys 29 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport -22.2 - 86.2 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

Trimethylphosphine oxide

Abdallaoui, H. E. Alaoui El; Rubini, P.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 49; nb. 3; (1993); p. 329 - 338, View in Reaxys

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30 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport -14 - 92 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

triphenylphosphineoxide

Abdallaoui, H. E. Alaoui El; Rubini, P.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 49; nb. 3; (1993); p. 329 - 338, View in Reaxys 31 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport -21 - 81.4 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

trimethyl phosphate

Abdallaoui, H. E. Alaoui El; Rubini, P.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 49; nb. 3; (1993); p. 329 - 338, View in Reaxys 32 of 63

Description (Transport Phenomena (MCS))

Diffusion

Partner (Transport Phenomena (MCS))

C12H18N2(1+)

Phelps, Donald K.; Ramm, Michael T.; Wang, Yichun; Nelsen, Stephen F.; Weaver, Michael J.; Journal of Physical Chemistry; vol. 97; nb. 1; (1993); p. 181 - 188, View in Reaxys 33 of 63

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport -5.1 - 39.9 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

2,6,10,15,19,23-hexamethyltetracosane

Olea, Andres F.; Thomas, J. K.; Journal of the American Chemical Society; vol. 110; nb. 14; (1988); p. 4494 4502, View in Reaxys 34 of 63

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport 19.9 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

n-heptane

Olea, Andres F.; Thomas, J. K.; Journal of the American Chemical Society; vol. 110; nb. 14; (1988); p. 4494 4502, View in Reaxys 35 of 63

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport 19.9 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

octanol

Olea, Andres F.; Thomas, J. K.; Journal of the American Chemical Society; vol. 110; nb. 14; (1988); p. 4494 4502, View in Reaxys 36 of 63

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport 19.9 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

decane

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Olea, Andres F.; Thomas, J. K.; Journal of the American Chemical Society; vol. 110; nb. 14; (1988); p. 4494 4502, View in Reaxys 37 of 63

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport 19.9 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

dodecane

Olea, Andres F.; Thomas, J. K.; Journal of the American Chemical Society; vol. 110; nb. 14; (1988); p. 4494 4502, View in Reaxys 38 of 63

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport 19.9 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

cetane

Olea, Andres F.; Thomas, J. K.; Journal of the American Chemical Society; vol. 110; nb. 14; (1988); p. 4494 4502, View in Reaxys 39 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

benzene

Yadava, Raja R.; Yadava, Sarvanand S.; Singh, Vishwa N.; Journal of Chemical & Engineering Data; vol. 33; nb. 4; (1988); p. 402 - 404, View in Reaxys 40 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

para-xylene

Yadava, Raja R.; Yadava, Sarvanand S.; Singh, Vishwa N.; Journal of Chemical & Engineering Data; vol. 33; nb. 4; (1988); p. 402 - 404, View in Reaxys 41 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

mesitylene

Yadava, Raja R.; Yadava, Sarvanand S.; Singh, Vishwa N.; Journal of Chemical & Engineering Data; vol. 33; nb. 4; (1988); p. 402 - 404, View in Reaxys 42 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

tetrachloromethane

Aminabhavi, T. M.; Manjeshwar, L. S.; Balundgi, R. H.; Journal of Chemical & Engineering Data; vol. 32; nb. 1; (1987); p. 50 - 52, View in Reaxys 43 of 63

Description (Transport Phenomena (MCS))

Viscosity

224/412

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Temperature (Transport 25 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

dimethyl sulfoxide

Aminabhavi, T. M.; Manjeshwar, L. S.; Balundgi, R. H.; Journal of Chemical & Engineering Data; vol. 32; nb. 1; (1987); p. 50 - 52, View in Reaxys 44 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 45 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

tetrachloromethane

Manjeshwar, Lata S.; Aminabhavi, Tejraj M.; Journal of Chemical & Engineering Data; vol. 32; nb. 4; (1987); p. 409 - 412, View in Reaxys 45 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 45 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

dimethyl sulfoxide

Manjeshwar, Lata S.; Aminabhavi, Tejraj M.; Journal of Chemical & Engineering Data; vol. 32; nb. 4; (1987); p. 409 - 412, View in Reaxys 46 of 63

Description (Transport Phenomena (MCS))

Viscosity

Partner (Transport Phenomena (MCS))

1070

Description (Transport Phenomena (MCS))

Viscosity

Luzkii; Obuchowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 2692,2512; Chem.Abstr.; vol. 57; nb. 64; (1962), View in Reaxys; Schroeder; Kintner; AIChE Journal; vol. 11; (1975); p. 5, View in Reaxys; Timofeeva et al.; Russian Journal of Physical Chemistry; vol. 53; (1979); p. 243; ; p. 447, View in Reaxys 48 of 63

Description (Transport Phenomena (MCS))

Diffusion

Anderson et al.; Journal of Physical Chemistry; vol. 76; (1972); p. 4006,4008, View in Reaxys; Czworniak et al.; Chemical Physics; vol. 11; (1975); p. 451,466,469, View in Reaxys; Avramenko et al.; Russian Journal of Physical Chemistry; vol. 49; (1975); p. 902; ; p. 1532, View in Reaxys 49 of 63

Description (Transport Phenomena (MCS))

Viscosity

Comment (Transport Phenomena (MCS))

Diagramm.

Partner (Transport Phenomena (MCS))

tetrachloromethane

Carman; Miller; Transactions of the Faraday Society; vol. 55; (1959); p. 1838,1840,1841, View in Reaxys 50 of 63

Description (Transport Phenomena (MCS))

Diffusion

Comment (Transport Phenomena (MCS))

Diagramm des Koeffizienten der gegenseitigen Diffusion und der Selbsdiffusionskoeffizienten.

Partner (Transport Phenomena (MCS))

tetrachloromethane

Carman; Miller; Transactions of the Faraday Society; vol. 55; (1959); p. 1838,1840,1841, View in Reaxys

225/412

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51 of 63

Description (Transport Phenomena (MCS))

Viscosity

Comment (Transport Phenomena (MCS))

Diagramm.

Partner (Transport Phenomena (MCS))

benzene

Miller; Carman; Transactions of the Faraday Society; vol. 55; (1959); p. 1831,1835,1836, View in Reaxys 52 of 63

Description (Transport Phenomena (MCS))

Diffusion

Comment (Transport Phenomena (MCS))

Diagramm des Koeffizienten der gegenseitigen Diffusion und der Selbsldiffusionskoeffizienten.

Partner (Transport Phenomena (MCS))

benzene

Miller; Carman; Transactions of the Faraday Society; vol. 55; (1959); p. 1831,1835,1836, View in Reaxys 53 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

Dichte von Gemischen.

Partner (Transport Phenomena (MCS))

chloral

Udowenko; Chomenko; Zhurnal Obshchei Khimii; vol. 27; (1957); p. 583; engl. Ausg. S. 649, View in Reaxys 54 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 50 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

Dichte von Gemischen.

Partner (Transport Phenomena (MCS))

chloral

Udowenko; Chomenko; Zhurnal Obshchei Khimii; vol. 27; (1957); p. 583; engl. Ausg. S. 649, View in Reaxys 55 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 75 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

Dichte von Gemischen.

Partner (Transport Phenomena (MCS))

chloral

Udowenko; Chomenko; Zhurnal Obshchei Khimii; vol. 27; (1957); p. 583; engl. Ausg. S. 649, View in Reaxys 56 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

Dichte von Gemischen.

Partner (Transport Phenomena (MCS))

aluminium trichloride

Galinker; Zhurnal Obshchei Khimii; vol. 26; (1956); p. 1564,1565;engl.Ausg.S.1753, View in Reaxys

226/412

2016-04-19 03:35:30

57 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 30 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

Dichte von Gemischen.

Partner (Transport Phenomena (MCS))

aluminium trichloride

Galinker; Zhurnal Obshchei Khimii; vol. 26; (1956); p. 1564,1565;engl.Ausg.S.1753, View in Reaxys 58 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 40 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

Dichte von Gemischen.

Partner (Transport Phenomena (MCS))

aluminium trichloride

Galinker; Zhurnal Obshchei Khimii; vol. 26; (1956); p. 1564,1565;engl.Ausg.S.1753, View in Reaxys 59 of 63

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

Dichte von Gemischen.

Partner (Transport Phenomena (MCS))

methanol

Miller; Fuoss; Journal of the American Chemical Society; vol. 75; (1953); p. 3076,3079, View in Reaxys 60 of 63

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

methanol

Comment (Transport Phenomena (MCS))

Diffusionsgeschwindigkeit.

Dummer; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 109; (1920); p. 39, View in Reaxys 61 of 63

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

nitrobenzene

Comment (Transport Phenomena (MCS))

Diffusionsgeschwindigkeit.

Dummer; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 109; (1920); p. 39, View in Reaxys 62 of 63

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

ethyl benzoate

Comment (Transport Phenomena (MCS))

Diffusionsgeschwindigkeit.

Dummer; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 109; (1920); p. 39, View in Reaxys 63 of 63

Description (Transport Phenomena (MCS))

Viscosity

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Temperature (Transport 25 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

6prozent Wasser; Dichte von Gemischen.

Partner (Transport Phenomena (MCS))

sulfuric acid; water

Liler; Kosanovic; Symp.Hydrogen Bonding Ljubljana 1957 S.529,531, View in Reaxys Vapour Pressure (12) Vapour Pressure Temperature (Va[Torr] pour Pressure) [°C]

Comment (Vapour Pressure)

References

177.914

Bittrich, H.-J.; Eckert, R.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 175; nb. 2; (1992); p. 217 - 234, View in Reaxys; Bittrich, H.-J.; Eckert, R.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 185; nb. 2; (1994); p. 207 222, View in Reaxys

0.0464

Hussam; Carr; Analytical Chemistry; vol. 57; nb. 4; (1985); p. 793 801, View in Reaxys Williams; Journal of the American Chemical Society; vol. 47; (1925); p. 2646, View in Reaxys; Sivtsova et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 38; (1965); p. 2609,2549, View in Reaxys; Berman; West; Journal of Chemical and Engineering Data; vol. 12; (1967); p. 197, View in Reaxys; Brown; Smith; Australian Journal of Chemistry; vol. 13; (1960); p. 30, View in Reaxys; Komarova; Kogan; J. Appl. Chem. USSR (Engl. Transl.); vol. 38; (1965); p. 2690,2629,2630, View in Reaxys; Marsh et al.; Journal of Chemical Thermodynamics; vol. 11; (1979); p. 897,899 - 901, View in Reaxys; Boublikova; Collection of Czechoslovak Chemical Communications; vol. 38; (1973); p. 2033, View in Reaxys equation exists.

Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys

116.38 - 767.09

49.9 - 101.4

Brown; Smith; Australian Journal of Chemistry; vol. 8; (1955); p. 62,65, View in Reaxys

149.41 - 2026

55.7 - 136.4

McCullough et al.; Journal of the American Chemical Society; vol. 76; (1954); p. 4791,4793,4794, View in Reaxys

25.31 - 28.73

18.6 - 21

Baughan et al.; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 225; (1954); p. 478,502, View in Reaxys

27.8

v.Schickh; Angewandte Chemie; vol. 62; (1950); p. 547,554, View in Reaxys; Gabriel; Industrial and Engineering Chemistry; vol. 32; (1940); p. 891, View in Reaxys

36.66

Jones; Giauque; Journal of the American Chemical Society; vol. 69; (1947); p. 984, View in Reaxys

21.9 - 47.6

15.5 - 30

Joukovsky; Bulletin des Societes Chimiques Belges; vol. 43; (1934); p. 401, View in Reaxys

25 - 100

v.Halban; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 84; (1913); p. 139, View in Reaxys

10 - 100

Holcomb; Dorsey; Industrial and Engineering Chemistry; vol. 41; p. 2790, View in Reaxys

16.12 - 730.4

NMR Spectroscopy (87) 1 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

14N

Solvents (NMR Spectro- cyclohexane scopy)

228/412

2016-04-19 03:35:30

Temperature (NMR Spectroscopy) [°C]

Witanowski, Michal; Biedrzycka, Zenobia; Grela, Karol; Wejroch, Krystyna; Magnetic Resonance in Chemistry; vol. 36; nb. SPEC. ISS.; (1998); p. S85-S92, View in Reaxys; Witanowski, Michal; Sicinska, Wanda; Biedrzycka, Zenobia; Webb, Graham A.; Journal of Molecular Structure; vol. 476; nb. 1-3; (1999); p. 133 - 138, View in Reaxys 2 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

15N

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectroscopy) [MHz]

50.75

Abbotto, Alessandro; Bradamante, Silvia; Facchetti, Antonio; Pagani, Giorgio A.; Journal of Organic Chemistry; vol. 64; nb. 18; (1999); p. 6756 - 6763, View in Reaxys 3 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

15N

Solvents (NMR Spectro- benzene-d6 scopy) Temperature (NMR Spectroscopy) [°C]

Wrackmeyer, Bernd; Kupce, Eriks; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 53; nb. 4; (1998); p. 411 - 415, View in Reaxys 4 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

14N

Solvents (NMR Spectro- acetone scopy) Temperature (NMR Spectroscopy) [°C]

Witanowski, Michal; Biedrzycka, Zenobia; Grela, Karol; Wejroch, Krystyna; Magnetic Resonance in Chemistry; vol. 36; nb. SPEC. ISS.; (1998); p. S85-S92, View in Reaxys 5 of 87

Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- benzene-d6 scopy) Temperature (NMR Spectroscopy) [°C]

Comment (NMR Spectroscopy)

13C-15N, 1H-15N.

Wrackmeyer, Bernd; Kupce, Eriks; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 53; nb. 4; (1998); p. 411 - 415, View in Reaxys 6 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- D2O scopy) Temperature (NMR Spectroscopy) [°C]

229/412

2016-04-19 03:35:30

Gottlieb, Hugo E.; Kotlyar, Vadim; Nudelman, Abraham; Journal of Organic Chemistry; vol. 62; nb. 21; (1997); p. 7512 - 7515, View in Reaxys 7 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- tetradeuteriomethanol scopy) Temperature (NMR Spectroscopy) [°C]

Gottlieb, Hugo E.; Kotlyar, Vadim; Nudelman, Abraham; Journal of Organic Chemistry; vol. 62; nb. 21; (1997); p. 7512 - 7515, View in Reaxys 8 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CD3CN scopy) Temperature (NMR Spectroscopy) [°C]

Gottlieb, Hugo E.; Kotlyar, Vadim; Nudelman, Abraham; Journal of Organic Chemistry; vol. 62; nb. 21; (1997); p. 7512 - 7515, View in Reaxys 9 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- benzene-d6 scopy) Temperature (NMR Spectroscopy) [°C]

Gottlieb, Hugo E.; Kotlyar, Vadim; Nudelman, Abraham; Journal of Organic Chemistry; vol. 62; nb. 21; (1997); p. 7512 - 7515, View in Reaxys 10 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- dimethylsulfoxide-d6 scopy) Temperature (NMR Spectroscopy) [°C]

Gottlieb, Hugo E.; Kotlyar, Vadim; Nudelman, Abraham; Journal of Organic Chemistry; vol. 62; nb. 21; (1997); p. 7512 - 7515, View in Reaxys 11 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- acetone-d6 scopy) Temperature (NMR Spectroscopy) [°C]

Gottlieb, Hugo E.; Kotlyar, Vadim; Nudelman, Abraham; Journal of Organic Chemistry; vol. 62; nb. 21; (1997); p. 7512 - 7515, View in Reaxys

230/412

2016-04-19 03:35:30

12 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Temperature (NMR Spectroscopy) [°C]

Gottlieb, Hugo E.; Kotlyar, Vadim; Nudelman, Abraham; Journal of Organic Chemistry; vol. 62; nb. 21; (1997); p. 7512 - 7515, View in Reaxys 13 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- D2O scopy) Temperature (NMR Spectroscopy) [°C]

Gottlieb, Hugo E.; Kotlyar, Vadim; Nudelman, Abraham; Journal of Organic Chemistry; vol. 62; nb. 21; (1997); p. 7512 - 7515, View in Reaxys 14 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- tetradeuteriomethanol scopy) Temperature (NMR Spectroscopy) [°C]

Gottlieb, Hugo E.; Kotlyar, Vadim; Nudelman, Abraham; Journal of Organic Chemistry; vol. 62; nb. 21; (1997); p. 7512 - 7515, View in Reaxys 15 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CD3CN scopy) Temperature (NMR Spectroscopy) [°C]

Gottlieb, Hugo E.; Kotlyar, Vadim; Nudelman, Abraham; Journal of Organic Chemistry; vol. 62; nb. 21; (1997); p. 7512 - 7515, View in Reaxys 16 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- benzene-d6 scopy) Temperature (NMR Spectroscopy) [°C]

Gottlieb, Hugo E.; Kotlyar, Vadim; Nudelman, Abraham; Journal of Organic Chemistry; vol. 62; nb. 21; (1997); p. 7512 - 7515, View in Reaxys 17 of 87

Description (NMR Spec- Chemical shifts troscopy)

231/412

2016-04-19 03:35:30

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- dimethylsulfoxide-d6 scopy) Temperature (NMR Spectroscopy) [°C]

Gottlieb, Hugo E.; Kotlyar, Vadim; Nudelman, Abraham; Journal of Organic Chemistry; vol. 62; nb. 21; (1997); p. 7512 - 7515, View in Reaxys 18 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- acetone-d6 scopy) Temperature (NMR Spectroscopy) [°C]

Gottlieb, Hugo E.; Kotlyar, Vadim; Nudelman, Abraham; Journal of Organic Chemistry; vol. 62; nb. 21; (1997); p. 7512 - 7515, View in Reaxys 19 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Temperature (NMR Spectroscopy) [°C]

Gottlieb, Hugo E.; Kotlyar, Vadim; Nudelman, Abraham; Journal of Organic Chemistry; vol. 62; nb. 21; (1997); p. 7512 - 7515, View in Reaxys 20 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

14N

Solvents (NMR Spectro- neat (no solvent) scopy) Witanowski, M.; Sicinska, W.; Biedrzycka, Z.; Grabowski, Z.; Webb, G. A.; Journal of Magnetic Resonance, Series A; vol. 112; nb. 1; (1995); p. 66 - 71, View in Reaxys; Witanowski, M.; Stefaniak, L.; Kamienski, B.; Biernat, S.; Webb, G. A.; Journal of Magnetic Resonance (1969-1992); vol. 43; nb. 3; (1981); p. 456 - 462, View in Reaxys 21 of 87

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

15N

Solvents (NMR Spectro- benzene-d6 scopy) Kupce, Eriks; Wrackmeyer, Bernd; Journal of Magnetic Resonance, Series A; vol. 101; nb. 3; (1993); p. 324 - 326, View in Reaxys 22 of 87

Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- benzene-d6 scopy) Comment (NMR Spectroscopy)

1H-15N, 13C-15N.

Kupce, Eriks; Wrackmeyer, Bernd; Journal of Magnetic Resonance, Series A; vol. 101; nb. 3; (1993); p. 324 - 326, View in Reaxys

232/412

2016-04-19 03:35:30

23 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

15N

Solvents (NMR Spectro- dimethylsulfoxide-d6 scopy) Temperature (NMR Spectroscopy) [°C]

Kolehmainen, Erkki; Laihia, Katri; Rissanen, Kari; Rasala, Danuta; Gawinecki, Ryszard; Magnetic Resonance in Chemistry; vol. 30; nb. 6; (1992); p. 527 - 534, View in Reaxys 24 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

15N

Solvents (NMR Spectro- benzene-d6 scopy) Temperature (NMR Spectroscopy) [°C]

23.9

Kupce, Eriks; Wrackmeyer, Bernd; Journal of Magnetic Resonance (1969-1992); vol. 97; nb. 3; (1992); p. 568 594, View in Reaxys 25 of 87

Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- benzene-d6 scopy) Temperature (NMR Spectroscopy) [°C]

23.9

Comment (NMR Spectroscopy)

13C-15N, 1H-15N.

Kupce, Eriks; Wrackmeyer, Bernd; Journal of Magnetic Resonance (1969-1992); vol. 97; nb. 3; (1992); p. 568 594, View in Reaxys 26 of 87

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

14N

Solvents (NMR Spectro- neat (no solvent) scopy) Temperature (NMR Spectroscopy) [°C]

20.9

Hayashi, Shigenobu; Hayamizu, Kikuko; Bulletin of the Chemical Society of Japan; vol. 64; nb. 2; (1991); p. 688 690, View in Reaxys 27 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

15N

Solvents (NMR Spectro- nitromethane; trifluoroacetic acid scopy) Johnston, James F.; Ridd, John H.; Sandall, John P. B.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 5; (1991); p. 623 - 628, View in Reaxys 28 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

14N

233/412

2016-04-19 03:35:30

Temperature (NMR Spectroscopy) [°C]

20.9

Hayashi, Shigenobu; Hayamizu, Kikuko; Bulletin of the Chemical Society of Japan; vol. 64; nb. 2; (1991); p. 688 690, View in Reaxys 29 of 87

Description (NMR Spec- Spin-spin coupling constants troscopy) Temperature (NMR Spectroscopy) [°C]

20.9

Comment (NMR Spectroscopy)

1H-14N.

Hayashi, Shigenobu; Hayamizu, Kikuko; Bulletin of the Chemical Society of Japan; vol. 64; nb. 2; (1991); p. 688 690, View in Reaxys 30 of 87

Description (NMR Spec- Linewidth of NMR absorption troscopy) Coburn, Michael D.; Storm, Carlyle B.; Moore, Donald W.; Archibald, Thomas G.; Magnetic Resonance in Chemistry; vol. 28; (1990); p. 16 - 20, View in Reaxys; Strelenko, Yu. A.; Torocheshnikov, V. N.; Sergeyev, N. M.; Journal of Magnetic Resonance (1969-1992); vol. 89; nb. 1; (1990); p. 123 - 128, View in Reaxys; Hayashi, Shigenobu; Hayamizu, Kikuko; Bulletin of the Chemical Society of Japan; vol. 64; nb. 2; (1991); p. 688 - 690, View in Reaxys; Gerothanassis, Ioannis P.; Lauterwein, Juergen; Magnetic Resonance in Chemistry; vol. 24; (1986); p. 1034 - 1038, View in Reaxys; Witanowski, M.; Stefaniak, L.; Kamienski, B.; Biernat, S.; Webb, G. A.; Journal of Magnetic Resonance (1969-1992); vol. 43; nb. 3; (1981); p. 456 - 462, View in Reaxys

31 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Holm; Journal of Chemical Physics; vol. 26; (1957); p. 707, View in Reaxys; Lauterbur; Journal of Chemical Physics; vol. 26; (1957); p. 217; Annals of the New York Academy of Sciences; vol. 70; (1957); p. 841,853, View in Reaxys; Strelenko, Yu. A.; Torocheshnikov, V. N.; Sergeyev, N. M.; Journal of Magnetic Resonance (1969-1992); vol. 89; nb. 1; (1990); p. 123 - 128, View in Reaxys 32 of 87

Description (NMR Spec- Spin-lattice relaxation time (T1) troscopy) Pendred et al.; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1966); p. 1009, View in Reaxys; Zweers et al.; Physica B+C: Physics of Condensed Matter + Atomic, Molecular and Plasma Physics, Optics (Amsterdam); vol. 85; (1977); p. 239,252, View in Reaxys; Strelenko, Yu. A.; Torocheshnikov, V. N.; Sergeyev, N. M.; Journal of Magnetic Resonance (1969-1992); vol. 89; nb. 1; (1990); p. 123 - 128, View in Reaxys

33 of 87

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Coburn, Michael D.; Storm, Carlyle B.; Moore, Donald W.; Archibald, Thomas G.; Magnetic Resonance in Chemistry; vol. 28; (1990); p. 16 - 20, View in Reaxys 34 of 87

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

15N

Strelenko, Yu. A.; Torocheshnikov, V. N.; Sergeyev, N. M.; Journal of Magnetic Resonance (1969-1992); vol. 89; nb. 1; (1990); p. 123 - 128, View in Reaxys 35 of 87

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

17O

Strelenko, Yu. A.; Torocheshnikov, V. N.; Sergeyev, N. M.; Journal of Magnetic Resonance (1969-1992); vol. 89; nb. 1; (1990); p. 123 - 128, View in Reaxys

234/412

2016-04-19 03:35:30

36 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

14N

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

14N

Strelenko, Yu. A.; Torocheshnikov, V. N.; Sergeyev, N. M.; Journal of Magnetic Resonance (1969-1992); vol. 89; nb. 1; (1990); p. 123 - 128, View in Reaxys; Comeau, M.; Beraldin, M.-T.; Vauthier, E. C.; Fliszar, S.; Canadian Journal of Chemistry; vol. 63; (1985); p. 3226 - 3232, View in Reaxys 38 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

15N

Strelenko, Yu. A.; Torocheshnikov, V. N.; Sergeyev, N. M.; Journal of Magnetic Resonance (1969-1992); vol. 89; nb. 1; (1990); p. 123 - 128, View in Reaxys 39 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

14N

Temperature (NMR Spectroscopy) [°C]

323

Strelenko, Yu. A.; Torocheshnikov, V. N.; Sergeyev, N. M.; Journal of Magnetic Resonance (1969-1992); vol. 89; nb. 1; (1990); p. 123 - 128, View in Reaxys 40 of 87

Description (NMR Spec- Spin-spin coupling constants troscopy) Comment (NMR Spectroscopy)

1H-13C

Strelenko, Yu. A.; Torocheshnikov, V. N.; Sergeyev, N. M.; Journal of Magnetic Resonance (1969-1992); vol. 89; nb. 1; (1990); p. 123 - 128, View in Reaxys; Everett, Jeremy R.; Organic Magnetic Resonance; vol. 19; nb. 3; (1982); p. 169 - 172, View in Reaxys 41 of 87

Description (NMR Spec- Spin-spin coupling constants troscopy) Comment (NMR Spectroscopy)

1H-15N

Strelenko, Yu. A.; Torocheshnikov, V. N.; Sergeyev, N. M.; Journal of Magnetic Resonance (1969-1992); vol. 89; nb. 1; (1990); p. 123 - 128, View in Reaxys 42 of 87

Description (NMR Spec- Spin-spin coupling constants troscopy) Comment (NMR Spectroscopy)

13C-14N

Strelenko, Yu. A.; Torocheshnikov, V. N.; Sergeyev, N. M.; Journal of Magnetic Resonance (1969-1992); vol. 89; nb. 1; (1990); p. 123 - 128, View in Reaxys 43 of 87

Description (NMR Spec- Spin-spin relaxation time (T2) troscopy) Strelenko, Yu. A.; Torocheshnikov, V. N.; Sergeyev, N. M.; Journal of Magnetic Resonance (1969-1992); vol. 89; nb. 1; (1990); p. 123 - 128, View in Reaxys

235/412

2016-04-19 03:35:30

44 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- aq. H2SO4 scopy) Bagno, Alessandro; Scorrano, Gianfranco; Journal of the American Chemical Society; vol. 110; nb. 14; (1988); p. 4577 - 4582, View in Reaxys 45 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) ITO, Haruko; ITO, Tasuku; Chemistry Letters; (1985); p. 1251 - 1254, View in Reaxys; Bailey, William F.; Cioffi, Eugene A.; Magnetic Resonance in Chemistry; vol. 25; (1987); p. 181 - 183, View in Reaxys 46 of 87

Description (NMR Spec- NMR with shift reagents troscopy) Beaute et al.; Journal of the Chemical Society [Section] D: Chemical Communications; (1971); p. 700, View in Reaxys; Gerothanassis, Ioannis P.; Lauterwein, Juergen; Magnetic Resonance in Chemistry; vol. 24; (1986); p. 1034 - 1038, View in Reaxys

47 of 87

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- neat (no solvent) scopy) Engelke, Ray; Earl, William L.; Rohlfing, Celeste McMichael; Journal of Physical Chemistry; vol. 90; nb. 4; (1986); p. 545 - 547, View in Reaxys; Engelke, Ray; Earl, William L.; Rohlfing, Celeste McMichael; Journal of Chemical Physics; vol. 84; nb. 1; (1986); p. 142 - 146, View in Reaxys 48 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectro- CCl4 scopy) Temperature (NMR Spectroscopy) [°C]

Gerothanassis, Ioannis P.; Lauterwein, Juergen; Magnetic Resonance in Chemistry; vol. 24; (1986); p. 1034 1038, View in Reaxys 49 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectro- CHCl3 scopy) Temperature (NMR Spectroscopy) [°C]

Gerothanassis, Ioannis P.; Lauterwein, Juergen; Magnetic Resonance in Chemistry; vol. 24; (1986); p. 1034 1038, View in Reaxys 50 of 87

Description (NMR Spec- Chemical shifts troscopy)

236/412

2016-04-19 03:35:30

Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectro- CH2Cl2 scopy) Temperature (NMR Spectroscopy) [°C]

Gerothanassis, Ioannis P.; Lauterwein, Juergen; Magnetic Resonance in Chemistry; vol. 24; (1986); p. 1034 1038, View in Reaxys 51 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectro- acetone scopy) Temperature (NMR Spectroscopy) [°C]

Gerothanassis, Ioannis P.; Lauterwein, Juergen; Magnetic Resonance in Chemistry; vol. 24; (1986); p. 1034 1038, View in Reaxys 52 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectro- dioxane scopy) Temperature (NMR Spectroscopy) [°C]

Gerothanassis, Ioannis P.; Lauterwein, Juergen; Magnetic Resonance in Chemistry; vol. 24; (1986); p. 1034 1038, View in Reaxys 53 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectro- methanol scopy) Temperature (NMR Spectroscopy) [°C]

Gerothanassis, Ioannis P.; Lauterwein, Juergen; Magnetic Resonance in Chemistry; vol. 24; (1986); p. 1034 1038, View in Reaxys 54 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectro- neat (no solvent) scopy) Temperature (NMR Spectroscopy) [°C]

Gerothanassis, Ioannis P.; Lauterwein, Juergen; Magnetic Resonance in Chemistry; vol. 24; (1986); p. 1034 1038, View in Reaxys 55 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

17O

237/412

2016-04-19 03:35:30

Solvents (NMR Spectro- H2O scopy) Temperature (NMR Spectroscopy) [°C]

Gerothanassis, Ioannis P.; Lauterwein, Juergen; Magnetic Resonance in Chemistry; vol. 24; (1986); p. 1034 1038, View in Reaxys 56 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CHCl3 scopy) Engelke, Ray; Earl, William L.; Rohlfing, Celeste McMichael; Journal of Chemical Physics; vol. 84; nb. 1; (1986); p. 142 - 146, View in Reaxys 57 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- methanol scopy) Engelke, Ray; Earl, William L.; Rohlfing, Celeste McMichael; Journal of Chemical Physics; vol. 84; nb. 1; (1986); p. 142 - 146, View in Reaxys 58 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- cyclohexane scopy) Engelke, Ray; Earl, William L.; Rohlfing, Celeste McMichael; Journal of Chemical Physics; vol. 84; nb. 1; (1986); p. 142 - 146, View in Reaxys 59 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) ITO, Haruko; ITO, Tasuku; Chemistry Letters; (1985); p. 1251 - 1254, View in Reaxys 60 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

14N

Solvents (NMR Spectro- methanol scopy) Temperature (NMR Spectroscopy) [°C]

34.7

Witanowski, M.; Sitkowski, J.; Biernat, S.; Kamienski, B.; Hamdi, B. T.; Webb, G. A.; Magnetic Resonance in Chemistry; vol. 23; nb. 9; (1985); p. 748 - 753, View in Reaxys 61 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

14N

Solvents (NMR Spectro- dimethylsulfoxide scopy)

238/412

2016-04-19 03:35:30

Temperature (NMR Spectroscopy) [°C]

34.7

Witanowski, M.; Sitkowski, J.; Biernat, S.; Kamienski, B.; Hamdi, B. T.; Webb, G. A.; Magnetic Resonance in Chemistry; vol. 23; nb. 9; (1985); p. 748 - 753, View in Reaxys 62 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- benzene-d6 scopy) Temperature (NMR Spectroscopy) [°C]

Everett, Jeremy R.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 7; (1984); p. 1151 - 1154, View in Reaxys 63 of 87

Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- benzene-d6 scopy) Temperature (NMR Spectroscopy) [°C]

Comment (NMR Spectroscopy)

13C-1H.

Everett, Jeremy R.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 7; (1984); p. 1151 - 1154, View in Reaxys 64 of 87

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

Temperature (NMR Spectroscopy) [°C]

-68.2

Chauvel, J. Paul; True, Nancy S.; Journal of Physical Chemistry; vol. 87; nb. 9; (1983); p. 1622 - 1625, View in Reaxys 65 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- various solvent(s) scopy) Al-Rawi, Jasim M. A.; Behnam, George Q.; Taha, Nihad I.; Organic Magnetic Resonance; vol. 16; nb. 3; (1981); p. 198 - 201, View in Reaxys 66 of 87

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

14N

Solvents (NMR Spectro- CD2Cl2 scopy) Temperature (NMR Spectroscopy) [°C]

Loewenstein, A.; Goldsmith, A. D.; Journal of Magnetic Resonance (1969-1992); vol. 41; nb. 2; (1980); p. 222 228, View in Reaxys 67 of 87

Description (NMR Spec- Spectrum troscopy)

239/412

2016-04-19 03:35:30

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CD2Cl2 scopy) Temperature (NMR Spectroscopy) [°C]

Loewenstein, A.; Goldsmith, A. D.; Journal of Magnetic Resonance (1969-1992); vol. 41; nb. 2; (1980); p. 222 228, View in Reaxys 68 of 87

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CD2Cl2 scopy) Temperature (NMR Spectroscopy) [°C]

Loewenstein, A.; Goldsmith, A. D.; Journal of Magnetic Resonance (1969-1992); vol. 41; nb. 2; (1980); p. 222 228, View in Reaxys 69 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- methanol; tetradeuteriomethanol scopy) Bowman, W. Russ; Golding, Bernard T.; Watson, William P.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1980); p. 731 - 736, View in Reaxys 70 of 87

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- ClSO2F scopy) Temperature (NMR Spectroscopy) [°C]

-60

Olah, George A.; Fung, Alexander P.; Rawdah, Tarik N.; Journal of Organic Chemistry; vol. 45; nb. 21; (1980); p. 4149 - 4153, View in Reaxys 71 of 87

Description (NMR Spec- NMR in liquid-crystal phase troscopy) Loewenstein, A.; Goldsmith, A. D.; Journal of Magnetic Resonance (1969-1992); vol. 41; nb. 2; (1980); p. 222 228, View in Reaxys

72 of 87

Description (NMR Spec- NMR troscopy) Lorand,J.P. et al.; Journal of Organic Chemistry; vol. 34; (1969); p. 4176 - 4178, View in Reaxys; Lippmaa,E.T. et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 20; (1971); p. 924 - 928; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 20; (1971); p. 1006 - 1011, View in Reaxys; Warren,J.P.; Roberts,J.D.; Journal of Physical Chemistry; vol. 78; (1974); p. 2507, View in Reaxys; Witanowski; Januszewski; Journal of the Chemical Society [Section] B: Physical Organic; (1967); p. 1062, View in Reaxys; Monitz; Gutowsky; Journal of Chemical Physics; vol. 38; (1963); p. 1155,1158, View in Reaxys; Zhuravlev et al.; Journal of Applied Spectroscopy; vol. 27; (1977); p. 1440,1441, View in Reaxys; Witanowski et al.; Journal of Magnetic Resonance (1969-1992); vol. 28; (1977); p. 217,218, View in Reaxys; Frost; Hall; Molecular Physics; vol. 10; (1966); p. 191, View in Reaxys; Lumbroso-Bader et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 67; (1970); p. 1829,1831, View in Reaxys; Nikki; Nakagawa; Bulletin of the Chemical Society of Japan; vol. 51; (1978); p. 3267,3269, View in Reaxys; Barclay et al.; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1969); p. 830, View in Reaxys; Cavanaugh; Dailey; Journal of Chemical Physics; vol. 34; (1961); p. 1099,1100, View in Reaxys; Poranski; Moniz; Journal of Physical Chemistry; vol. 71; (1967); p. 1142, View in Reaxys; Nagy et al.; Bulletin des Societes Chimiques Belges; vol. 78; (1969); p. 639,

240/412

2016-04-19 03:35:30

View in Reaxys; Knunjanz et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1966); p. 1013; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1966); p. 1062, View in Reaxys; Deno et al.; Journal of Organic Chemistry; vol. 31; (1966); p. 1968, View in Reaxys; Jouve et al.; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 259; (1964); p. 119, View in Reaxys; Cyr; Cyr; Journal of Chemical Physics; vol. 47; (1967); p. 3082, View in Reaxys; Hammel; Smith; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1970); p. 1852, View in Reaxys; Frankiss; Journal of Physical Chemistry; vol. 67; (1963); p. 752,753, View in Reaxys; Pogorelyi; Divnich; Zhurnal Organicheskoi Khimii; vol. 11; (1975); p. 2007,2037, View in Reaxys; Ray; Journal of Chemical Physics; vol. 40; (1964); p. 3440, View in Reaxys; Anderson; Journal of Chemical Physics; vol. 50; (1969); p. 1474, View in Reaxys; Macomber et al.; Journal of Chemical Physics; vol. 46; (1967); p. 2855, View in Reaxys; Herbison-Evans; Richards; Molecular Physics; vol. 8; (1964); p. 19,26, View in Reaxys; Herbison-Evans; Richards; Molecular Physics; vol. 7; (1963); p. 515,520,522, View in Reaxys; Hilbers; MacLean; Molecular Physics; vol. 16; (1969); p. 275,278, View in Reaxys; Lichter; Journal of Magnetic Resonance (1969-1992); vol. 18; (1975); p. 367, View in Reaxys; Hilbers et al.; Pure and Applied Chemistry; vol. 32; (1972); p. 197,199,202, View in Reaxys; Kukhtenko et al.; Theoretical and Experimental Chemistry; vol. 10; (1974); p. 212; ; p. 267, View in Reaxys; Suchanski; Canepa; Journal of Magnetic Resonance (1969-1992); vol. 33; (1979); p. 389, View in Reaxys; Pang; Soon NG; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 29; (1973); p. 207, View in Reaxys; Saito et al.; Canadian Journal of Chemistry; vol. 51; (1973); p. 2118,2121, View in Reaxys; Armstrong et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1973); p. 1362, View in Reaxys; Armstrong et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1973); p. 1272,1273, View in Reaxys; Jallali-Heravi et al.; Organic Magnetic Resonance; vol. 12; (1979); p. 274,276, View in Reaxys; Gerace; Fung; Journal of Chemical Physics; vol. 53; (1970); p. 2984, View in Reaxys; Ramshaw et al.; Journal of Chemical Physics; vol. 54; (1971); p. 1239,1244, View in Reaxys; Breitmaier et al.; Tetrahedron; vol. 29; (1973); p. 2485,2486,2488, View in Reaxys; Inamoto; Masuda; Tetrahedron Letters; (1977); p. 3287, View in Reaxys; Wendschuh et al.; Tetrahedron Letters; (1973); p. 2931, View in Reaxys; Briggs et al.; Journal of the Chemical Society [Section] D: Chemical Communications; (1971); p. 680, View in Reaxys; Cheremisin; Schastnev; Journal of Structural Chemistry; vol. 19; (1978); p. 313; ; p. 364, View in Reaxys; Andersson; Mason; Chemical Communications (London); (1968); p. 99, View in Reaxys; Zoltewicz; O'Halloran; Journal of Organic Chemistry; vol. 39; (1974); p. 89,90, View in Reaxys; Spiesecke; Schneider; Journal of Chemical Physics; vol. 35; (1961); p. 731,732,733, View in Reaxys; Mason; van Bronswijk; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1970); p. 1763,1765, View in Reaxys; Henneike; Drago; Inorganic Chemistry; vol. 7; (1968); p. 1908,1909, View in Reaxys; Doddrell et al.; Australian Journal of Chemistry; vol. 27; (1974); p. 2175,2190, View in Reaxys; Healy; Morris; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 31; (1975); p. 1695, View in Reaxys 73 of 87

Description (NMR Spec- Spectrum troscopy) Comment (NMR Spectroscopy)

14N

Biemond et al.; Chemical Physics Letters; vol. 32; (1975); p. 390,391, View in Reaxys 74 of 87

Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)

15N

Lichter; Journal of Magnetic Resonance (1969-1992); vol. 18; (1975); p. 367, View in Reaxys 75 of 87

Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)

NMR chemical shifts

Moniz; Poranski; jr.; Journal of Magnetic Resonance (1969-1992); vol. 11; (1973); p. 62, View in Reaxys 76 of 87

Description (NMR Spec- Spin-spin coupling constants troscopy) Haake,P. et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 3577 - 3578, View in Reaxys; Colli et al.; Journal of the Chemical Society, Chemical Communications; (1973); p. 408, View in Reaxys; Barfield et al.; Journal of the American Chemical Society; vol. 83; (1961); p. 4726,4727, View in Reaxys

77 of 87

Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)

13C-chem. Verschiebung: exp. und berechnet nach CNDO/2

Sasaki; Suzuki; Chemical and Pharmaceutical Bulletin; vol. 20; (1972); p. 2522, View in Reaxys

241/412

2016-04-19 03:35:30

78 of 87

Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)

d. CH3-Protonen (Acn./CH3NO2) in Abh. v. d. LiClO4-Konz.

Wong et al.; Journal of Physical Chemistry; vol. 75; (1971); p. 56, View in Reaxys 79 of 87

Description (NMR Spec- Spectrum troscopy) Comment (NMR Spectroscopy)

Einfluss des Deuterierungsprozesses auf NMR-Spektrum

Martin et al.; Bulletin de la Societe Chimique de France; (1970); p. 4082, View in Reaxys 80 of 87

Description (NMR Spec- Spectrum troscopy) Sasaki; Suzuki; Chemical and Pharmaceutical Bulletin; vol. 17; (1969); p. 1778,1780, View in Reaxys; Witanowski et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 2569,2570, View in Reaxys; Hofman et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 554,555, View in Reaxys; Jouve; Tonnard; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 259; (1964); p. 3753, View in Reaxys; Hammond; Journal of the Chemical Society; (1963); p. 2565, View in Reaxys

81 of 87

Description (NMR Spec- Spectrum troscopy) Comment (NMR Spectroscopy)

Untersuchung

Sasaki; Suzuki; Chemical and Pharmaceutical Bulletin; vol. 17; (1969); p. 2049,2050, View in Reaxys 82 of 87

Description (NMR Spec- Spectrum troscopy) Comment (NMR Spectroscopy)

des nach γ-Bestrahlung bei 77K erhaltenen Radikals

Chachaty; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 262; (1966); p. 680, View in Reaxys 83 of 87

Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)

chem. Verschiebung in Neopentan und Benzol

Schneider; Journal of Physical Chemistry; vol. 66; (1962); p. 2653,2656, View in Reaxys 84 of 87

Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)

'chemical shift' der Methylprotonen in Cyclohexan u. Cyclohexan + Bzl., Py., Dioxan od. CCl4 bei 11-12grad; 'solvent shift' der Methylprotonen bei 11-12grad (Loesungsm. wie oben)

Nakagawa; Fujiwara; Bulletin of the Chemical Society of Japan; vol. 34; (1961); p. 143, View in Reaxys 85 of 87

Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)

1H (in versch. Loesm.)

Nakagawa; Nippon Kagaku Zasshi; vol. 82; (1961); p. 141,142; Chem.Abstr.; nb. 16157; (1961), View in Reaxys 86 of 87

Description (NMR Spec- Spin-spin coupling constants troscopy) Comment (NMR Spectroscopy)

nucleus1-nucleus2:13C-1H.

Muller; Pritchard; Journal of Chemical Physics; vol. 31; (1959); p. 1471,1472, View in Reaxys; Lauterbur; Journal of Chemical Physics; vol. 26; (1957); p. 217; Annals of the New York Academy of Sciences; vol. 70; (1957); p. 841,853, View in Reaxys 87 of 87

Description (NMR Spec- Chemical shifts troscopy)

242/412

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Nucleus (NMR Spectroscopy)

Dailey; Shoolery; Journal of the American Chemical Society; vol. 77; (1955); p. 3977,3980, View in Reaxys; Tiers; Journal of Physical Chemistry; vol. 62; (1958); p. 1151, View in Reaxys; Allred; Rochow; Journal of the American Chemical Society; vol. 79; (1957); p. 5361,5362, View in Reaxys; Rocard; Franke; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 246; (1958); p. 2466, View in Reaxys; Meyer et al.; Journal of the American Chemical Society; vol. 75; (1953); p. 4567,4570, View in Reaxys IR Spectroscopy (71) 1 of 71

Description (IR Spectroscopy)

Bands; Spectrum

Solvent (IR Spectroscopy)

sodium chloride

Greenwald; Kalagaev; Tetrahedron Letters; vol. 51; nb. 19; (2010); p. 2610 - 2612, View in Reaxys 2 of 71

Description (IR Spectroscopy)

FT-IR-Difference Spectroscopy; Spectrum

Solvent (IR Spectroscopy)

potassium bromide

Citroni, Margherita; Bini, Roberto; Pagliai, Marco; Cardini, Gianni; Schettino, Vincenzo; Journal of Physical Chemistry B; vol. 114; nb. 29; (2010); p. 9420 - 9428, View in Reaxys 3 of 71

Description (IR Spectroscopy)

Spectrum

Brannon; Hayden; Journal of the Association of Official Agricultural Chemists; vol. 47; (1964); p. 918,927, View in Reaxys; Luzkii; Scheremet'ewa; Russian Journal of Physical Chemistry; vol. 41; (1967); p. 403; Zhurnal Fizicheskoi Khimii; vol. 41; (1967); p. 776, View in Reaxys; Krueger; Mettee; Canadian Journal of Chemistry; vol. 42; (1964); p. 288,289, View in Reaxys; Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys; Allerhand; von Rague-Schleyer; Journal of the American Chemical Society; vol. 85; (1963); p. 1715,1717, View in Reaxys; Jones; Sheppard; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 304; (1968); p. 135, View in Reaxys; Singh; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 23; (1967); p. 439,444, View in Reaxys; DeMaine; Journal of Molecular Spectroscopy; vol. 4; (1960); p. 407,408, View in Reaxys; Wong et al.; Journal of Physical Chemistry; vol. 75; (1971); p. 56, View in Reaxys; Soussen-Jacob et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 67; (1970); p. 1118,1120 - 1122, 1124, View in Reaxys; Karyakin et al.; Russian Journal of Physical Chemistry; vol. 44; (1970); p. 1179, View in Reaxys; Fialkov et al.; Sov. Prog. Chem. (Engl. Transl.); vol. 35; nb. 12; (1969); p. 1269,29, View in Reaxys; Shverina; Rozen; Russian Journal of Physical Chemistry; vol. 52; (1978); p. 461; ; p. 800, View in Reaxys; Verdermame et al.; Journal of Chemical Physics; vol. 56; (1972); p. 2638, View in Reaxys; Belin; Potier; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 69; (1972); p. 1222,1223,1224,1226,1227, View in Reaxys; Kevan; Park; Cho; Physical Chemistry Chemical Physics; vol. 3; nb. 15; (2001); p. 3247 - 3253, View in Reaxys 4 of 71

Description (IR Spectroscopy)

Spectrum

Temperature (IR Spectroscopy) [°C]

-193.15

Shilina; Kuramshina; Smirnov; Rostovshchikova; Russian Chemical Bulletin; vol. 50; nb. 7; (2001); p. 1159 1165, View in Reaxys 5 of 71

Description (IR Spectroscopy)

Bands

Temperature (IR Spectroscopy) [°C]

-193.15

Shilina; Kuramshina; Smirnov; Rostovshchikova; Russian Chemical Bulletin; vol. 50; nb. 7; (2001); p. 1159 1165, View in Reaxys 6 of 71

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

gas

Nanba; Obuchi; Izumi; Sugiura; Xu; Uchisawa; Kushiyama; Chemical Communications; nb. 2; (2001); p. 173 174, View in Reaxys

243/412

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7 of 71

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

3500 - 500 1/cm

Deak, John C.; Iwaki, Lawrence K.; Dlott, Dana D.; Journal of Physical Chemistry A: Molecules, Spectroscopy, Kinetics, Environment, & General Theory; vol. 103; nb. 8; (1999); p. 971 - 979, View in Reaxys 8 of 71

Description (IR Spectroscopy)

Overtone spectrum

Halonen; Callegari; Lehmann; Journal of Physical Chemistry A; vol. 102; nb. 46; (1998); p. 9124 - 9128, View in Reaxys 9 of 71

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

gaseous matrix

Temperature (IR Spectroscopy) [°C]

26.9

Comment (IR Spectroscopy)

16780 - 2850 cm**(-1)

Cavagnat; Lespade; Journal of Chemical Physics; vol. 106; nb. 19; (1997); p. 7946 - 7957, View in Reaxys 10 of 71

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

1620 - 1550 cm**(-1)

Pal, Chandramadhab; Hazra, Anindya; Ghosh, Pradip N.; Kshirsagar; Journal of Molecular Structure; vol. 407; nb. 2-3; (1997); p. 165 - 170, View in Reaxys 11 of 71

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

gaseous matrix

Comment (IR Spectroscopy)

16504 - 2974 cm**(-1)

Cavagnat; Lespade; Journal of Chemical Physics; vol. 106; nb. 19; (1997); p. 7946 - 7957, View in Reaxys 12 of 71

Description (IR Spectroscopy)

Fine structure of IR bands

Pal, Chandramadhab; Hazra, Anindya; Ghosh, Pradip N.; Kshirsagar; Journal of Molecular Structure; vol. 407; nb. 2-3; (1997); p. 165 - 170, View in Reaxys 13 of 71

Description (IR Spectroscopy)

Intensity of IR bands

Singh; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 23; (1967); p. 439,444, View in Reaxys; Jogansen et al.; Optics and Spectroscopy; vol. 18; (1965); p. 18; ; p. 38, View in Reaxys; Iogansen; Litovchenko; Doklady Physical Chemistry; vol. 148-153; (1963); p. 1129; Doklady Akademii Nauk SSSR; vol. 153; (1963); p. 1367, View in Reaxys; Lopatin, B. V.; Shorygin, P. P.; Gorodilova, T. E.; Journal of Applied Spectroscopy; vol. 50; nb. 6; (1989); p. 602 - 605; Zhurnal Prikladnoi Spektroskopii; vol. 50; nb. 6; (1989); p. 950 - 954, View in Reaxys; Schmidt, W.; Brunn, J.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 270; nb. 1; (1989); p. 42 - 48, View in Reaxys; Dommen, Joseph; Forster, Martin; Rupreccht, Heidi; Bauder, Alfred; Guenthard, Hans-Heinrich; Helvetica Chimica Acta; vol. 65; nb. 2; (1982); p. 504 - 520, View in Reaxys; Chen, Sheah; Hong, Xiaoyu; Hill, Jeffrey R.; Dlott, Dana D.; Journal of Physical Chemistry; vol. 99; nb. 13; (1995); p. 4525 - 4530, View in Reaxys 14 of 71

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

gas

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Temperature (IR Spectroscopy) [°C]

24.9

Comment (IR Spectroscopy)

950 - 880 cm**(-1)

Cataliotti, R. S.; Distefano, M. R.; Mariani, L.; Morresi, A.; Paliani, G.; et al.; Berichte der Bunsen-Gesellschaft; vol. 98; nb. 12; (1994); p. 1613 - 1618, View in Reaxys 15 of 71

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

gas

Temperature (IR Spectroscopy) [°C]

24.9

Comment (IR Spectroscopy)

700 - 620 cm**(-1)

Cataliotti, R. S.; Distefano, M. R.; Mariani, L.; Morresi, A.; Paliani, G.; et al.; Berichte der Bunsen-Gesellschaft; vol. 98; nb. 12; (1994); p. 1613 - 1618, View in Reaxys 16 of 71

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

918 - 657 cm**(-1)

Cataliotti, R. S.; Distefano, M. R.; Mariani, L.; Morresi, A.; Paliani, G.; et al.; Berichte der Bunsen-Gesellschaft; vol. 98; nb. 12; (1994); p. 1613 - 1618, View in Reaxys 17 of 71

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

gas

Temperature (IR Spectroscopy) [°C]

24.9

Comment (IR Spectroscopy)

3200 - 2800 cm**(-1)

Gorse, Dominique; Cavagnat, Dominique; Pesquer, Michel; Lapouge, Christine; Journal of Physical Chemistry; vol. 97; nb. 17; (1993); p. 4262 - 4269, View in Reaxys 18 of 71

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

gas

Temperature (IR Spectroscopy) [°C]

24.9

Comment (IR Spectroscopy)

3080 - 475 cm**(-1)

Gorse, Dominique; Cavagnat, Dominique; Pesquer, Michel; Lapouge, Christine; Journal of Physical Chemistry; vol. 97; nb. 17; (1993); p. 4262 - 4269, View in Reaxys 19 of 71

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

CCl4

Comment (IR Spectroscopy)

3100 - 600 cm**(-1)

Cataliotti, R. S.; Paliani, G.; Mariani, L.; Santini, S.; Giorgini, M. G.; Journal of Physical Chemistry; vol. 96; nb. 7; (1992); p. 2961 - 2964, View in Reaxys

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20 of 71

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

gas

Comment (IR Spectroscopy)

3100 - 600 cm**(-1)

Cataliotti, R. S.; Paliani, G.; Mariani, L.; Santini, S.; Giorgini, M. G.; Journal of Physical Chemistry; vol. 96; nb. 7; (1992); p. 2961 - 2964, View in Reaxys 21 of 71

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

3100 - 600 cm**(-1)

Cataliotti, R. S.; Paliani, G.; Mariani, L.; Santini, S.; Giorgini, M. G.; Journal of Physical Chemistry; vol. 96; nb. 7; (1992); p. 2961 - 2964, View in Reaxys 22 of 71

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CCl4

Comment (IR Spectroscopy)

2954 - 656 cm**(-1)

Cataliotti, R. S.; Paliani, G.; Mariani, L.; Santini, S.; Giorgini, M. G.; Journal of Physical Chemistry; vol. 96; nb. 7; (1992); p. 2961 - 2964, View in Reaxys 23 of 71

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

gas

Comment (IR Spectroscopy)

2953 - 657 cm**(-1)

Cataliotti, R. S.; Paliani, G.; Mariani, L.; Santini, S.; Giorgini, M. G.; Journal of Physical Chemistry; vol. 96; nb. 7; (1992); p. 2961 - 2964, View in Reaxys 24 of 71

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

2954 - 657 cm**(-1)

Cataliotti, R. S.; Paliani, G.; Mariani, L.; Santini, S.; Giorgini, M. G.; Journal of Physical Chemistry; vol. 96; nb. 7; (1992); p. 2961 - 2964, View in Reaxys 25 of 71

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CCl4

Comment (IR Spectroscopy)

3043 - 2953 cm**(-1)

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

dimethylsulfoxide-d6

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Comment (IR Spectroscopy)

3024 - 2945 cm**(-1)

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

acetone-d6

Comment (IR Spectroscopy)

3042 - 2957 cm**(-1)

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

benzene-d6

Comment (IR Spectroscopy)

3030 - 2952 cm**(-1)

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CD3NO2

Comment (IR Spectroscopy)

3046 - 2957 cm**(-1)

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CD3CN

Comment (IR Spectroscopy)

3043 - 2957 cm**(-1)

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

4000 - 400 cm**(-1)

Hill, J. R.; Moore, D. S.; Schmidt, S. C.; Storm, C. B.; Journal of Physical Chemistry; vol. 95; nb. 8; (1991); p. 3037 - 3044, View in Reaxys 32 of 71

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

various solvent(s)

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Comment (IR Spectroscopy)

1600 - 1300 cm**(-1)

Belhakem, M.; Jordanov, B.; Journal of Molecular Structure; vol. 245; nb. 3.4; (1991); p. 195 - 202, View in Reaxys 33 of 71

Description (IR Spectroscopy)

Polarization of IR bands

Belhakem, M.; Jordanov, B.; Journal of Molecular Structure; vol. 245; nb. 3.4; (1991); p. 195 - 202, View in Reaxys 34 of 71

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

various solvent(s)

Temperature (IR Spectroscopy) [°C]

-196.2 - 21.9

Comment (IR Spectroscopy)

1200 - 1050 cm**(-1)

Remizov, A. B.; Stolov, A. A.; Fishman, A. I.; Russian Journal of Physical Chemistry; vol. 63; nb. 6; (1989); p. 837 - 839; Zhurnal Fizicheskoi Khimii; vol. 63; (1989); p. 1513 - 1516, View in Reaxys 35 of 71

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

11600 - 11300 cm**(-1)

Schmidt, W.; Brunn, J.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 270; nb. 1; (1989); p. 42 - 48, View in Reaxys 36 of 71

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Temperature (IR Spectroscopy) [°C]

24.9

Comment (IR Spectroscopy)

3600 - 450 cm**(-1)

Miller, P. J.; Block, S.; Piermarini, G. J.; Journal of Physical Chemistry; vol. 93; nb. 1; (1989); p. 462 - 466, View in Reaxys 37 of 71

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

solid

Temperature (IR Spectroscopy) [°C]

21.9

Comment (IR Spectroscopy)

3500 - 700 cm**(-1)

Piermarini, G. J.; Block, S.; Miller, P. J.; Journal of Physical Chemistry; vol. 93; nb. 1; (1989); p. 457 - 462, View in Reaxys 38 of 71

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Temperature (IR Spectroscopy) [°C]

129.9

Comment (IR Spectroscopy)

1500 - 700 cm**(-1)

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Piermarini, G. J.; Block, S.; Miller, P. J.; Journal of Physical Chemistry; vol. 93; nb. 1; (1989); p. 457 - 462, View in Reaxys 39 of 71

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CCl4

Temperature (IR Spectroscopy) [°C]

-196.2 - 21.9

Comment (IR Spectroscopy)

1400 - 655 cm**(-1)

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

various solvent(s)

Comment (IR Spectroscopy)

1000 - 800 cm**(-1)

Skulski, Lech; Przybylowicz, Jaroslaw; Bulletin of the Polish Academy of Sciences, Chemistry; vol. 32; nb. 11-12; (1984); p. 483 - 499, View in Reaxys 41 of 71

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

5556 - 4762 cm**(-1)

Bacelon, P.; Corset, J.; Loze, C. de; Journal of Solution Chemistry; vol. 12; nb. 1; (1983); p. 1 - 12, View in Reaxys 42 of 71

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

3021 - 2955 cm**(-1)

Bacelon, P.; Corset, J.; Loze, C. de; Journal of Solution Chemistry; vol. 12; nb. 1; (1983); p. 1 - 12, View in Reaxys 43 of 71

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Temperature (IR Spectroscopy) [°C]

4.9

Comment (IR Spectroscopy)

3200 - 2800 cm**(-1)

Knoezinger; Kollhoff; Wittenbeck; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 86; nb. 10; (1982); p. 929 - 935, View in Reaxys 44 of 71

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

gaseous matrix

Temperature (IR Spectroscopy) [°C]

-269

Comment (IR Spectroscopy)

1574 cm**(-1)

249/412

2016-04-19 03:35:30

Dommen, Joseph; Forster, Martin; Rupreccht, Heidi; Bauder, Alfred; Guenthard, Hans-Heinrich; Helvetica Chimica Acta; vol. 65; nb. 2; (1982); p. 504 - 520, View in Reaxys 45 of 71

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

654 - 3600 cm**(-1)

Brasch, J. W.; Journal of Physical Chemistry; vol. 84; nb. 16; (1980); p. 2084 - 2085, View in Reaxys 46 of 71

Description (IR Spectroscopy)

Spectrum

Temperature (IR Spectroscopy) [°C]

-175

Comment (IR Spectroscopy)

200 - 20 cm**(-1)

Brodskii, I. A.; Libov, V. S.; Perova, T. S.; Shcherbinin, M. B.; Russian Journal of Physical Chemistry; vol. 54; nb. 5; (1980); p. 678 - 681; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 5; (1980); p. 1187 - 1190, View in Reaxys 47 of 71

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Temperature (IR Spectroscopy) [°C]

Comment (IR Spectroscopy)

200 - 20 cm**(-1)

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

1111 - 909 cm**(-1)

Avouris, Phaedon; Chan, I. Y.; Loy, M. M. T.; Journal of Chemical Physics; vol. 72; nb. 6; (1980); p. 3522 - 3527, View in Reaxys 49 of 71

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Temperature (IR Spectroscopy) [°C]

Comment (IR Spectroscopy)

80 cm**(-1)

Description (IR Spectroscopy)

Lorand,J.P. et al.; Journal of Organic Chemistry; vol. 34; (1969); p. 4176 - 4178, View in Reaxys; Barakat et al.; Transactions of the Faraday Society; vol. 59; (1963); p. 1773, View in Reaxys; Fini; Mirone; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 32; (1976); p. 625,626, View in Reaxys; Dragulescu et al.; Monatshefte fuer Chemie; vol. 105; (1974); p. 1170,1172,1173, View in Reaxys; Niven; Court; Applied Spectroscopy; vol. 24; (1970); p. 296, View in Reaxys; Iogansen; Litovchenko; Journal of Applied Spectroscopy; vol. 2; (1965); p. 159; ; p. 243, View in Reaxys; Mauret et al.; Bulletin de la Societe Chimique de France; (1974); p. 379, View in Reaxys; Nowikow et al.; Tetrahedron, Supplement; vol. 6; (1964); p. 119,128; Chem.Abstr.; nb. 14665; (1965), View in Reaxys; Jouve et al.; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 259; (1964); p. 119, View in Reaxys; Varsanyi et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 23; (1967); p. 1205,1210, View in Reaxys; Watarai et al.; Bulletin of the Chemical Society of Ja-

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pan; vol. 40; (1967); p. 1448,1449, View in Reaxys; Su; Hong; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 1461,1464, View in Reaxys; Jakobsen; Brasch; Journal of the American Chemical Society; vol. 86; (1964); p. 3571, View in Reaxys; Suzuki; Suzuki; Bulletin of the Chemical Society of Japan; vol. 42; (1969); p. 3394, View in Reaxys; Jones et al.; Canadian Journal of Chemistry; vol. 40; (1962); p. 334, View in Reaxys; Yarwood; Orville-Thomas; Journal of the Chemical Society; (1963); p. 5991, View in Reaxys; Halmann; Pinchas; Journal of the Chemical Society; (1960); p. 1246, View in Reaxys; Ungnade et al.; Journal of Physical Chemistry; vol. 64; (1960); p. 1410,1414, View in Reaxys; Diop et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 73; (1976); p. 207,208-211, View in Reaxys; Higuchi et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 28; (1972); p. 1335,1338, View in Reaxys; Bhujee; Randhawa; Indian Journal of Chemistry; vol. 10; (1972); p. 945, View in Reaxys; Dahkis et al.; Journal of Molecular Structure; vol. 13; (1972); p. 339,341,346, View in Reaxys; Geiseler; Kessler; Nitro Compounds., Proc. Intern. Symp.; (1964); p. 187 - 194; Chem.Abstr.; vol. 64; nb. 1928f; (1966), View in Reaxys; Yoshida; Takabayashi; Nippon Kagaku Zasshi; vol. 87; (1966); p. 452,453,454, View in Reaxys; Wendschuh et al.; Tetrahedron Letters; (1973); p. 2931, View in Reaxys; Kinugasa; Nakashima; Nippon Kagaku Zasshi; vol. 86; (1965); p. 497; Chem.Abstr.; vol. 63; nb. 5506; (1965), View in Reaxys; Lopatin; Theoretical and Experimental Chemistry; vol. 13; (1977); p. 399, View in Reaxys; Kroon; van der Elsken; Chemical Physics Letters; vol. 1; (1967); p. 285, View in Reaxys; Low; Freeman; Analytical Chemistry; vol. 39; (1967); p. 194, View in Reaxys; Iogansen; Litovchenko; Optics and Spectroscopy; vol. 16; (1964); p. 380; ; p. 700, View in Reaxys; McKean; Watt; Journal of Molecular Spectroscopy; vol. 61; nb. 2; (1976); p. 184 - 202, View in Reaxys; Remizov; Musyakaeva; Optics and Spectroscopy; vol. 38; (1975); p. 226; ; p. 399, View in Reaxys 51 of 71

Description (IR Spectroscopy)

Bands

de Maine et al.; Canadian Journal of Chemistry; vol. 38; (1960); p. 1921,1923, View in Reaxys; Geiseler et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 1007,1008, View in Reaxys; Baitinger et al.; Tetrahedron; vol. 20; (1964); p. 1635,1639, View in Reaxys; Jones; Wood; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1966); p. 1448, View in Reaxys; Osipov et al.; Journal of Applied Spectroscopy; vol. 8; (1968); p. 598; ; p. 1003, View in Reaxys; Popov; Shlyapochnikov; Optics and Spectroscopy; vol. 15; (1963); p. 174; ; p. 325, View in Reaxys 52 of 71

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

1105 cm**(-1); Intensitaet bei -20grad und +80grad.

Bashulin; Smirnow; Optika i Spektroskopiya; vol. 6; (1959); p. 745,749;engl.Ausg.S.485,487, View in Reaxys 53 of 71

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

917 cm**(-1); Intensitaet bei -20grad und +80grad.

Bashulin; Smirnow; Optika i Spektroskopiya; vol. 6; (1959); p. 745,749;engl.Ausg.S.485,487, View in Reaxys 54 of 71

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

5000 - 667 cm**(-1); des Dampfes.

Pierson et al.; Analytical Chemistry; vol. 28; (1956); p. 1218,1222; A. P. I. Res. Project; vol. 44; nb. 1220; (1951), View in Reaxys 55 of 71

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

5000 - 667 cm**(-1); fluessig.

A.P.I.; Res.Project; vol. 44; nb. 1751; (1956), View in Reaxys 56 of 71

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CHCl3

Comment (IR Spectroscopy)

NO2-Streckschwingungsbanden.

Brown; Journal of the American Chemical Society; vol. 77; (1955); p. 6341,6344, View in Reaxys 57 of 71

Description (IR Spectroscopy)

Bands

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Solvent (IR Spectroscopy)

ethanol

Comment (IR Spectroscopy)

NO2-Streckschwingungsbanden.

Luther; Guenzler; Zeitschrift fuer Naturforschung; vol. 10b; (1955); p. 445,449, View in Reaxys 58 of 71

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

NO2-Streckschwingungsbanden der Fluessigkeit.

Haszeldine; Journal of the Chemical Society; (1953); p. 2525, View in Reaxys 59 of 71

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

5000 - 455 cm**(-1); des Dampfes.

Smith et al.; Journal of Chemical Physics; vol. 18; (1950); p. 706,707,712, View in Reaxys 60 of 71

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

5000 - 455 cm**(-1); fluessig.

Smith et al.; Journal of Chemical Physics; vol. 18; (1950); p. 706,707,712, View in Reaxys 61 of 71

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

1667 - 1333 cm**(-1); von fluessigem Nitromethan.

Lenormant; Clement; Bulletin de la Societe Chimique de France; (1946); p. 652,565, View in Reaxys 62 of 71

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

10000 - 690 cm**(-1); von fluessigem Nitromethan.

Nielsen; Smith; Industrial and Engineering Chemistry, Analytical Edition; vol. 15; (1943); p. 610, View in Reaxys 63 of 71

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

des Natriumsalzes.

Mathieu; Massignon; Annales de Physique (Paris, France); vol. <11>16; (1941); p. 10,12,13; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 212; (1941); p. 1085, View in Reaxys 64 of 71

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

10000 - 6250 cm**(-1); von fluessigem Nitromethan.

Suhrmann; Klein; Zeitschrift fuer Physikalische Chemie, Abteilung B: Chemie der Elementarprozesse, Aufbau der Materie; vol. 50; (1941); p. 50, View in Reaxys 65 of 71

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

1667 - 690 cm**(-1); von fluessigem Nitromethan.

Description (IR Spectroscopy)

Spectrum

252/412

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Comment (IR Spectroscopy)

3333 - 400 cm**(-1); von gasfoermigem Nitromethan.

Wells; Wilson; Journal of Chemical Physics; vol. 9; (1941); p. 314, View in Reaxys 67 of 71

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

4000 - 1075 cm**(-1); von gasfoermigem Nitromethan.

Bogdan; Stefanescu; Bl.Soc.roum Phys.; vol. 42; (1941); p. 73; Chem.Abstr.; (1943); p. 3669, View in Reaxys 68 of 71

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

12500 - 3571 cm**(-1); von fluessigem Nitromethan.

Corin; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 33; (1936); p. 452,454; Bulletin de la Societe Royale des Sciences de Liege; vol. 10; (1941); p. 101; Chem.Abstr.; (1945); p. 4548, View in Reaxys 69 of 71

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

3333 - 2778 cm**(-1); von fluessigem Nitromethan.

Plyler; Burdine; Physical Review; vol. <2>35; (1930); p. 609,610, View in Reaxys 70 of 71

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

1786 - 1351 cm**(-1); von fluessigem Nitromethan.

Plyler; Burdine; Physical Review; vol. <2>35; (1930); p. 609,610, View in Reaxys 71 of 71

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

10000 - 667 cm**(-1)

Coblentz,W.W.; Investigations of Infra-red Spectra<Washington 1905>,S.140,157,187, View in Reaxys Mass Spectrometry (20) Description (Mass Comment (Mass Spectrometry) Spectrometry)

References

spectrum; time-offlight mass spectra (TOFMS); negative ion spectroscopy

Woods III, Ephraim; Dessiaterik, Yury; Miller, Roger E.; Baer, Tomas; Journal of Physical Chemistry A; vol. 105; nb. 36; (2001); p. 8273 - 8280, View in Reaxys

spectrum; time-offlight mass spectra (TOFMS); positive secondary ions

Woods III, Ephraim; Dessiaterik, Yury; Miller, Roger E.; Baer, Tomas; Journal of Physical Chemistry A; vol. 105; nb. 36; (2001); p. 8273 - 8280, View in Reaxys

spectrum

Egsgaard; Carlsen; Elbel; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 90; nb. 4; (1986); p. 369 - 374, View in Reaxys; Kilic; Ledingham; Kosmidis; McCanny; Singhal; Wang; Smith; Langley; Shaikh; Journal of Physical Chemistry A; vol. 101; nb. 5; (1997); p. 817 - 823, View in Reaxys; Blais; Engelke; Sheffield; Journal of Physical Chemistry A; vol. 101; nb. 44; (1997); p. 8285 - 8295, View in Reaxys

spectrum; chemical ionization (CI)

Kadentsev; Kolotyrkina; Stomakhin; Chizhov; Shevelev; Russian Chemical Bulletin; vol. 46; nb. 6; (1997); p. 1184 - 1185, View in Reaxys

fragmentation pattern

charge exchange with positive ions

Beijersbergen, Jaap H. M.; Zande, Wim J. van der; Kistemaker, Piet G.; Los, Joop; Drewello, Thomas; Nibbering, Nico M. M.; Journal of Physical Chemistry; vol. 96; nb. 23; (1992); p. 9288 - 9293, View in Reaxys

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spectrum; electron impact (EI)

Reid, C. J.; Organic Mass Spectrometry; vol. 26; nb. 5; (1991); p. 402 - 409, View in Reaxys

spectrum

collisional activation

Qian, Kuangnan; Shukla, Anil; Futrell, Jean; Journal of the American Chemical Society; vol. 113; nb. 19; (1991); p. 7121 - 7129, View in Reaxys; Hop, Cornelis E. C. A.; Chen, Hongwen; Ruttink, P. J. A.; Holmes, John L.; Organic Mass Spectrometry; vol. 26; nb. 8; (1991); p. 679 - 687, View in Reaxys

spectrum

metastable ions

Hop, Cornelis E. C. A.; Chen, Hongwen; Ruttink, P. J. A.; Holmes, John L.; Organic Mass Spectrometry; vol. 26; nb. 8; (1991); p. 679 - 687, View in Reaxys

electron impact (EI); spectrum

Vairamani, M.; Organic Mass Spectrometry; vol. 25; nb. 5; (1990); p. 271 - 273, View in Reaxys; Egsgaard, Helge; Carlsen, Lars; Florencio, Helena; Drewello, Thomas; Schwarz, Helmut; Berichte der Bunsen-Gesellschaft; vol. 93; (1989); p. 76 - 80, View in Reaxys

electron impact (EI)

Gandhi, Suketu R.; Xu, Qi-Xun; Curtiss, Thomas J.; Bernstein, Richard B.; Journal of Physical Chemistry; vol. 91; nb. 21; (1987); p. 5437 - 5441, View in Reaxys

fragmentation pattern; spectrum

Wodtke, A. M.; Hintsa, E. J.; Lee, Y. T.; Journal of Physical Chemistry; vol. 90; nb. 16; (1986); p. 3549 - 3558, View in Reaxys

fragmentation pattern

collisional activation; metastable ions

Egsgaard; Carlsen; Elbel; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 90; nb. 4; (1986); p. 369 - 374, View in Reaxys

electron impact (EI)

metastable ions; charge exchange with positive ions

Morisson, James D.; Stanney, Keith; Tedder, John M.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1981); p. 967 969, View in Reaxys Haney; Franklin; Journal of Chemical Physics; vol. 48; (1968); p. 4093,4096, View in Reaxys; Patent; Boschan, Smith, U.S. Dep. Comm. Off. Tech. Serv. Rep.; US151120; (1957); Chem.Abstr.; nb. 10497; (1960), View in Reaxys; Sen Sharma; Franklin; International Journal of Mass Spectrometry and Ion Physics; vol. 13; (1974); p. 139, View in Reaxys; Lipei; Potapov; High Energy Chemistry; vol. 9; (1975); p. 290; ; p. 332, View in Reaxys; Bohme et al.; Journal of the American Chemical Society; vol. 94; (1972); p. 5153,5155, View in Reaxys; Aplin et al.; Journal of the American Chemical Society; vol. 87; (1965); p. 3180,3182, View in Reaxys; Meyerson; Fields; Organic Mass Spectrometry; vol. 9; (1974); p. 485,486, View in Reaxys; McAllister; Pitman; International Journal of Mass Spectrometry and Ion Physics; vol. 19; (1976); p. 241, View in Reaxys; Fileleeva et al.; Theoretical and Experimental Chemistry; vol. 11; (1975); p. 283,285, View in Reaxys; Knof et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 27; (1972); p. 162,165, View in Reaxys; Dawson et al.; International Journal of Mass Spectrometry and Ion Physics; vol. 11; (1973); p. 61,68, View in Reaxys; Mackay; Bohme; International Journal of Mass Spectrometry and Ion Physics; vol. 26; (1978); p. 327,331, 333, 337, View in Reaxys; Laramee et al.; International Journal of Mass Spectrometry and Ion Physics; vol. 31; (1979); p. 333,340, View in Reaxys

appearance potentials

Goldenfeld et al.; International Journal of Mass Spectrometry and Ion Physics; vol. 13; (1974); p. 297,303, View in Reaxys; Jaeger; Henglein; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 22; (1967); p. 700, View in Reaxys

negative ion spectroscopy

Tang et al.; International Journal of Mass Spectrometry and Ion Physics; vol. 14; (1974); p. 79,84, View in Reaxys

ion-cyclotron resonance

Kriemler; Buttrill; Journal of the American Chemical Society; vol. 95; (1973); p. 1365, View in Reaxys

appearance potentials

Elektronenstoss

Kandel; Journal of Chemical Physics; vol. 23; (1955); p. 84,85, View in Reaxys; Collin; Bulletin de la Societe Royale des Sciences de Liege; vol. 23; (1954); p. 194 - 196, View in Reaxys

positiver Ionen bei Fragmentierung durch Elektronenstoss.

Kandel; Journal of Chemical Physics; vol. 23; (1955); p. 84,85, View in Reaxys; Collin; Bulletin de la Societe Royale des Sciences de Liege; vol. 23; (1954); p. 194 - 196, View in Reaxys

UV/VIS Spectroscopy (33)

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1 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

neat (no solvent)

Comment (UV/VIS Spectroscopy)

300 - 550 nm

Winey; Gupta; Journal of Physical Chemistry A; vol. 101; nb. 49; (1997); p. 9333 - 9340, View in Reaxys 2 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

gas

Comment (UV/VIS Spectroscopy)

620.73 - 595.95 nm

Cavagnat, D.; Lespade, L.; Lapouge, C.; Berichte der Bunsen-Gesellschaft; vol. 99; nb. 3; (1995); p. 544 - 547, View in Reaxys 3 of 33

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

gas

Absorption Maxima (UV/ 612; 609.01; 605.91 VIS) [nm] Cavagnat, D.; Lespade, L.; Lapouge, C.; Berichte der Bunsen-Gesellschaft; vol. 99; nb. 3; (1995); p. 544 - 547, View in Reaxys 4 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

300 - 500 nm

Constantinou, C. P.; Winey, J. M.; Gupta, Y. M.; Journal of Physical Chemistry; vol. 98; nb. 32; (1994); p. 7767 7776, View in Reaxys 5 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

H2O

Comment (UV/VIS Spectroscopy)

200 - 320 nm

Bilski, Piotr; Reszka, Krzysztof; Chignell, Colin F.; Journal of the American Chemical Society; vol. 116; nb. 22; (1994); p. 9883 - 9889, View in Reaxys 6 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

aq. NaOH

Comment (UV/VIS Spectroscopy)

200 - 320 nm

Bilski, Piotr; Reszka, Krzysztof; Chignell, Colin F.; Journal of the American Chemical Society; vol. 116; nb. 22; (1994); p. 9883 - 9889, View in Reaxys 7 of 33

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

aq. NaOH

Absorption Maxima (UV/ 240 VIS) [nm] Ext./Abs. Coefficient [l·mol-1cm-1]

7500

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Bilski, Piotr; Reszka, Krzysztof; Chignell, Colin F.; Journal of the American Chemical Society; vol. 116; nb. 22; (1994); p. 9883 - 9889, View in Reaxys 8 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

acetonitrile

Comment (UV/VIS Spectroscopy)

238.1 - 192.31 nm

Phillips, David L.; Myers, Anne B.; Journal of Physical Chemistry; vol. 95; nb. 19; (1991); p. 7164 - 7171, View in Reaxys 9 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

H2O

Comment (UV/VIS Spectroscopy)

238.1 - 192.31 nm

Phillips, David L.; Myers, Anne B.; Journal of Physical Chemistry; vol. 95; nb. 19; (1991); p. 7164 - 7171, View in Reaxys 10 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

cyclohexane

Comment (UV/VIS Spectroscopy)

238.1 - 192.31 nm

Phillips, David L.; Myers, Anne B.; Journal of Physical Chemistry; vol. 95; nb. 19; (1991); p. 7164 - 7171, View in Reaxys 11 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

gas

Comment (UV/VIS Spectroscopy)

238.1 - 192.31 nm

Phillips, David L.; Myers, Anne B.; Journal of Physical Chemistry; vol. 95; nb. 19; (1991); p. 7164 - 7171, View in Reaxys 12 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

100 - 400 nm

Flicker, Wayne M.; Mosher, Oren A.; Kuppermann, Aron; Journal of Chemical Physics; vol. 72; nb. 4; (1980); p. 2788 - 2794, View in Reaxys 13 of 33

Description (UV/VIS Spectroscopy)

UV/VIS

Gast; Estes; Analytical Chemistry; vol. 32; (1960); p. 1712, View in Reaxys; Ungnade et al.; Journal of Physical Chemistry; vol. 68; (1964); p. 3226, View in Reaxys; Nagakura; Molecular Physics; vol. 3; (1960); p. 152,153-162; Chem.Abstr.; vol. 55; nb. 103; (1961), View in Reaxys; Balasubramanian; Rao; Spectrochimica Acta; vol. 18; (1962); p. 1337; Chem.Abstr.; vol. 55; nb. 3419; (1961), View in Reaxys; Barth et al.; Journal of the Chemical Society, Chemical Communications; (1975); p. 672, View in Reaxys; Burshtein; Slovetskii; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 27; (1978); p. 1300; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 27; (1978); p. 1487, View in Reaxys; Paszyc et al.; Journal of Photochemistry; vol. 9; (1978); p. 331, View in Reaxys; Barth et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1979); p. 907,908, View in Reaxys; Lopatin; Theoretical and Experimental Chemistry; vol. 13; (1977); p. 399, View in Reaxys; Belikov et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 20; (1971); p. 272,275; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 20; (1971); p. 335, View in Reaxys; Kamalov et al.; Doklady Chemistry; vol. 232; (1977); p. 68,69,70; Dokl. Akad. Nauk SSSR Ser. Khim.; vol. 232; (1977); p. 1077, View in Reaxys; Marciniak et al.; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 27; (1979); p.

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853,854,857, View in Reaxys; Tsenter; Bobovich; Sov. Phys. Dokl. (Engl. Transl.); vol. 7; (1963); p. 333,816, View in Reaxys 14 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Hedley; Chemische Berichte; vol. 41; (1908); p. 1196, View in Reaxys; Baly; Desch; Journal of the Chemical Society; vol. 93; (1908); p. 1750, View in Reaxys; Williams et al.; Journal of Organic Chemistry; vol. 30; (1965); p. 2674,2675, View in Reaxys; Ungnade et al.; Journal of Physical Chemistry; vol. 68; (1964); p. 3226, View in Reaxys; Loos et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 25; (1969); p. 275,277, View in Reaxys; Nagakura; Molecular Physics; vol. 3; (1960); p. 152,153-162; Chem.Abstr.; vol. 55; nb. 103; (1961), View in Reaxys; De Maine; Ahlers; Journal of the Chemical Society; (1960); p. 211, View in Reaxys; DeMaine; Journal of Molecular Spectroscopy; vol. 4; (1960); p. 407,408, View in Reaxys; Ungnade et al.; Journal of Physical Chemistry; vol. 64; (1960); p. 1410,1414, View in Reaxys; Bhujee; Randhawa; Indian Journal of Chemistry; vol. 10; (1972); p. 945, View in Reaxys; Mc Allister; Journal of Chemical Physics; vol. 57; (1972); p. 3353, View in Reaxys; Kuhn et al.; Helvetica Chimica Acta; vol. 54; (1971); p. 2260,2265-2266, 2273-2274, View in Reaxys; Jarosiewicz; Szychlinski; Roczniki Chemii; vol. 48; (1974); p. 1545,1546, 1548, 1550, View in Reaxys 15 of 33

Description (UV/VIS Spectroscopy)

Absorption maxima

Bonnafous; Labarre; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 66; (1969); p. 1376, View in Reaxys; Bayliss; Wills-Johnson; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 551,553, View in Reaxys; Halmann; Pinchas; Journal of the Chemical Society; (1960); p. 1246, View in Reaxys 16 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

CCl4

Pestemer; Fruhwirth; Monatshefte fuer Chemie; vol. 70; (1937); p. 155, View in Reaxys; Bayliss; Brackenridge; Journal of the American Chemical Society; vol. 77; (1955); p. 3559,3960, View in Reaxys; De Maine et al.; Transactions of the Faraday Society; vol. 53; (1957); p. 427,428, View in Reaxys; Bayliss; McRae; Journal of Physical Chemistry; vol. 58; (1954); p. 1006,1008, View in Reaxys 17 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

cyclohexane

De Maine et al.; Transactions of the Faraday Society; vol. 53; (1957); p. 427,428, View in Reaxys 18 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Urbanski; Ciecierska; Roczniki Chemii; vol. 29; (1955); p. 11,14,15; Chem.Abstr.; (1955); p. 11414, View in Reaxys; Zelinski; Rosanow; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 78; (1912); p. 630, View in Reaxys; Burawoy; Journal of the Chemical Society; (1939); p. 1185; Journal of the Chemical Society; (1941); p. 21, View in Reaxys; Hantzsch; Voigt; Chemische Berichte; vol. 45; (1912); p. 85,112; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 79; (1912); p. 597, View in Reaxys; Bayliss; McRae; Journal of Physical Chemistry; vol. 58; (1954); p. 1006,1008, View in Reaxys; Grammaticakis; Bulletin de la Societe Chimique de France; (1950); p. 158,159; Bulletin de la Societe Chimique de France; (1951); p. 220,221, View in Reaxys 19 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

H2O

Zelinski; Rosanow; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 78; (1912); p. 630, View in Reaxys; Kortuem; Z.phys.Chem.; vol. 50; (1941); p. 363, View in Reaxys; Bayliss; Brackenridge; Journal of the American Chemical Society; vol. 77; (1955); p. 3559,3960, View in Reaxys; Bayliss; McRae; Journal of Physical Chemistry; vol. 58; (1954); p. 1006,1008, View in Reaxys 20 of 33

Description (UV/VIS Spectroscopy)

Spectrum

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Solvent (UV/VIS Spectroscopy)

dioxane

Bayliss; Brackenridge; Journal of the American Chemical Society; vol. 77; (1955); p. 3559,3960, View in Reaxys 21 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

methanol

Bayliss; Brackenridge; Journal of the American Chemical Society; vol. 77; (1955); p. 3559,3960, View in Reaxys 22 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

toluene

Bayliss; Brackenridge; Journal of the American Chemical Society; vol. 77; (1955); p. 3559,3960, View in Reaxys 23 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

heptane

Bayliss; Brackenridge; Journal of the American Chemical Society; vol. 77; (1955); p. 3559,3960, View in Reaxys 24 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

2,2,4-trimethyl-pentane

Bayliss; Brackenridge; Journal of the American Chemical Society; vol. 77; (1955); p. 3559,3960, View in Reaxys 25 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

benzene

Bayliss; Brackenridge; Journal of the American Chemical Society; vol. 77; (1955); p. 3559,3960, View in Reaxys; Bayliss; McRae; Journal of Physical Chemistry; vol. 58; (1954); p. 1006,1008, View in Reaxys 26 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

H2SO4

Hantzsch; Voigt; Chemische Berichte; vol. 45; (1912); p. 85,112; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 79; (1912); p. 597, View in Reaxys; Bayliss; McRae; Journal of Physical Chemistry; vol. 58; (1954); p. 1006,1008, View in Reaxys 27 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

CHCl3

Bayliss; McRae; Journal of Physical Chemistry; vol. 58; (1954); p. 1006,1008, View in Reaxys 28 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

light petroleum

Jander; Haszeldine; Journal of the Chemical Society; (1954); p. 919,922, View in Reaxys 29 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

des Dampfes.

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Thompson; Pukis; Transactions of the Faraday Society; vol. 32; (1936); p. 678; Chem. Zentralbl.; vol. 108; nb. II; (1937); p. 955, View in Reaxys; Bayliss; McRae; Journal of Physical Chemistry; vol. 58; (1954); p. 1006,1008, View in Reaxys 30 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

aq. NaOH

Kortuem; Finckh; Zeitschrift fuer Physikalische Chemie, Abteilung B: Chemie der Elementarprozesse, Aufbau der Materie; vol. 48; (1941); p. 45, View in Reaxys; Kortuem; Z.phys.Chem.; vol. 43; (1939); p. 273,279,281, View in Reaxys; Hantzsch; Voigt; Chemische Berichte; vol. 45; (1912); p. 85,112; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 79; (1912); p. 597, View in Reaxys 31 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

aq. HCl

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

Spektrum des Dampfes bei 45grad bis 90grad unter 843-933 mm Druck.

Purvis; McCleland; Journal of the Chemical Society; vol. 103; (1913); p. 1105, View in Reaxys 33 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

alkali

Zelinski; Rosanow; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 78; (1912); p. 630, View in Reaxys ESR Spectroscopy (3) 1 of 3

Description (ESR Spectroscopy)

Spectrum

Shapiro et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1969); p. 405; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1969); p. 458, View in Reaxys; Shiotani et al.; Bulletin of the Chemical Society of Japan; vol. 49; (1976); p. 2154,2156, View in Reaxys; Trofimov; Chkheidze; High Energy Chemistry; vol. 1; (1967); p. 409, View in Reaxys; Madden, Keith P.; Taniguchi, Hitoshi; Fessenden, Richard W.; Journal of the American Chemical Society; vol. 110; nb. 9; (1988); p. 2753 - 2758, View in Reaxys 2 of 3

Description (ESR Spectroscopy)

g-factor

Madden, Keith P.; Taniguchi, Hitoshi; Fessenden, Richard W.; Journal of the American Chemical Society; vol. 110; nb. 9; (1988); p. 2753 - 2758, View in Reaxys 3 of 3

Description (ESR Spectroscopy)

ESR

Eiben; Fessenden; Journal of Physical Chemistry; vol. 75; (1971); p. 1186,1194, View in Reaxys; Neta et al.; Journal of Physical Chemistry; vol. 75; (1971); p. 1654,1661, View in Reaxys; Gilbert; Treuwith; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1973); p. 2010,2013, View in Reaxys; Eiben; Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie; vol. 29; (1974); p. 562, View in Reaxys NQR Spectroscopy (2) Description (NQR References Spectroscopy) Nuclear quadrupole resonance

Subbarao et al.; Physics Letters A; vol. 42; (1973); p. 461, View in Reaxys; Subbarao; Bray; Journal of Chemical Physics; vol. 67; (1977); p. 3947, View in Reaxys

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Nuclear quadrupole coupling constants

Cox; Waring; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 68; (1972); p. 1060, View in Reaxys

Rotational Spectroscopy (4) Description (Rota- Comment (Rota- References tional Spectrosco- tional Spectroscopy) py) Rotational spectrum

Riehn; Kunitski; Matylitsky; Gelin; Brutschy; Physical Chemistry Chemical Physics; vol. 7; nb. 23; (2005); p. 3955 - 3962, View in Reaxys

Microwave spectrum

Bak; Knudsen; Madsen; Physical Review; vol. <2>75; (1949); p. 1622; Chem.Abstr.; (1949); p. 5310, View in Reaxys; Dailey; Wilson; Physical Review; vol. <2>72; (1947); p. 522, View in Reaxys; Erlandsson; Ark.Fysik; vol. 6; (1953); p. 69, View in Reaxys; Cox; Waring; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 68; (1972); p. 1060, View in Reaxys; Rohart; Journal of Molecular Spectroscopy; vol. 57; (1975); p. 301, View in Reaxys; Cox, A. P.; Journal of Molecular Structure; vol. 97; (1983); p. 61 - 76, View in Reaxys; Soerensen, G. O.; Pedersen, T.; Dreizler, H.; Guarnieri, A.; Cox, A. Peter; Journal of Molecular Structure; vol. 97; (1983); p. 77 - 82, View in Reaxys

Intensity of microwave bands

Dommen, Joseph; Forster, Martin; Rupreccht, Heidi; Bauder, Alfred; Guenthard, Hans-Heinrich; Helvetica Chimica Acta; vol. 65; nb. 2; (1982); p. 504 - 520, View in Reaxys

Microwave spectrum

bei 30000-34000 MHz.

Tannenbaum et al.; Journal of Chemical Physics; vol. 25; (1956); p. 42,44, View in Reaxys

Raman Spectroscopy (26) Description (Ram- Solvent (Raman an Spectroscopy) Spectroscopy)

Comment (Raman Spectroscopy)

References

Spectrum

solid

single cryst.

Ouillon; Pinan-Lucarre; Ranson; Baranovic; Journal of Chemical Physics; vol. 116; nb. 11; (2002); p. 4611 - 4625, View in Reaxys

Spectrum

neat liquid

ambient temperature. Object(s) of Study: high pressure

Winey; Duvall; Knudson; Gupta; Journal of Chemical Physics; vol. 113; nb. 17; (2000); p. 7492 - 7501, View in Reaxys

Spectrum

Petrikaln; Ph.Ch.; vol. 3; p. 362, View in Reaxys; Petrikaln; Hochberg; Ph.Ch.; vol. 3; p. 224,405, View in Reaxys; Ganesan; Venkateswaran; Chem. Zentralbl.; vol. 100; nb. II; (1929); p. 2646, View in Reaxys; Wells; Wilson; Journal of Chemical Physics; vol. 9; (1941); p. 314, View in Reaxys; Medard; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 32; (1935); p. 137, View in Reaxys; Pendl; Reitz; Sabathy; Proceedings - Indian Academy of Sciences, Section A; vol. 8; (1938); p. 511; Chem. Zentralbl.; vol. 110; nb. II; (1939); p. 1855, View in Reaxys; Mathieu; Massignon; Annales de Physique (Paris, France); vol. <11>16; (1941); p. 10,12,13; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 212; (1941); p. 1085, View in Reaxys; Wittek; Zeitschrift fuer Physikalische Chemie, Abteilung B: Chemie der Elementarprozesse, Aufbau der Materie; vol. 51; (1942); p. 188,197, View in Reaxys; Dadieu; Kohlrausch; Monatshefte fuer Chemie; vol. 55; (1930); p. 379,399; Chemische Berichte; vol. 63; (1930); p. 251,260, View in Reaxys; Bobovich; Bortkevich; Journal of Applied Spectroscopy; vol. 9; (1965); p. 750; ; p. 144, View in Reaxys; Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys; Wong et al.; Journal of Physical Chemistry; vol. 75; (1971); p. 56, View in Reaxys; Kanesaka et al.; Journal of Chemical Physics; vol. 70; (1979); p. 5773, View in Reaxys; Tsenter; Bobovich; Optics and Spectroscopy; vol. 12; (1962); p. 25; ; p. 54, View in Reaxys; Belin; Potier; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 69; (1972); p. 1222,1223,1224,1226,1227, View in Reaxys; Pangilinan, G. I.; Gupta, Y. M.; Journal of Physical Chemistry; vol. 98; nb. 17; (1994); p. 4522 - 4529, View in Reaxys; Mohacek Grosev, Vlasta; Stelzer, Franz; Jocham, Daniel; Journal of Molecular Structure; vol. 476; nb. 1-3; (1999); p. 181 - 189, View in Reaxys solid

Deak, John C.; Iwaki, Lawrence K.; Dlott, Dana D.; Journal of Physical Chemistry A: Molecules, Spectroscopy, Kinetics, Environ-

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ment, & General Theory; vol. 103; nb. 8; (1999); p. 971 - 979, View in Reaxys Spectrum

neat (no solvent)

Hill, J. R.; Moore, D. S.; Schmidt, S. C.; Storm, C. B.; Journal of Physical Chemistry; vol. 95; nb. 8; (1991); p. 3037 - 3044, View in Reaxys; Cataliotti, R. S.; Paliani, G.; Mariani, L.; Santini, S.; Giorgini, M. G.; Journal of Physical Chemistry; vol. 96; nb. 7; (1992); p. 2961 - 2964, View in Reaxys; Miller, P. J.; Block, S.; Piermarini, G. J.; Journal of Physical Chemistry; vol. 93; nb. 1; (1989); p. 462 - 466, View in Reaxys; Cataliotti, R. S.; Distefano, M. R.; Mariani, L.; Morresi, A.; Paliani, G.; et al.; Berichte der Bunsen-Gesellschaft; vol. 98; nb. 12; (1994); p. 1613 - 1618, View in Reaxys; Courtecuisse, Stephane; Cansell, Francois; Fabre, Denise; Petitet, Jean-Pierre; Journal of Chemical Physics; vol. 102; nb. 2; (1995); p. 968 - 974, View in Reaxys; Courtecuisse, Stephane; Cansell, Francois; Fabre, Denise; Petitet, Jean Pierre; Journal of Chemical Physics; vol. 108; nb. 17; (1998); p. 7350 - 7355, View in Reaxys; Winey; Gupta; Journal of Physical Chemistry B; vol. 101; nb. 50; (1997); p. 10733 - 10743, View in Reaxys

Bands

neat (no solvent)

Hill, J. R.; Moore, D. S.; Schmidt, S. C.; Storm, C. B.; Journal of Physical Chemistry; vol. 95; nb. 8; (1991); p. 3037 - 3044, View in Reaxys; Cataliotti, R. S.; Paliani, G.; Mariani, L.; Santini, S.; Giorgini, M. G.; Journal of Physical Chemistry; vol. 96; nb. 7; (1992); p. 2961 - 2964, View in Reaxys; Cataliotti, Rosario Sergio; Foggi, Paolo; Giorgini, Maria Grazia; Mariani, Leonardo; Morresi, Assunta; Paliani, Giulio; Journal of Chemical Physics; vol. 98; nb. 6; (1993); p. 4372 - 4376, View in Reaxys; Courtecuisse, Stephane; Cansell, Francois; Fabre, Denise; Petitet, Jean-Pierre; Journal of Chemical Physics; vol. 102; nb. 2; (1995); p. 968 - 974, View in Reaxys; Courtecuisse, Stephane; Cansell, Francois; Fabre, Denise; Petitet, Jean Pierre; Journal of Chemical Physics; vol. 108; nb. 17; (1998); p. 7350 - 7355, View in Reaxys

Raman intensities

Tsenter; Bobovich; Optics and Spectroscopy; vol. 16; (1964); p. 134; ; p. 246, View in Reaxys; Pangilinan, G. I.; Gupta, Y. M.; Journal of Physical Chemistry; vol. 98; nb. 17; (1994); p. 4522 - 4529, View in Reaxys; Chen, Sheah; Hong, Xiaoyu; Hill, Jeffrey R.; Dlott, Dana D.; Journal of Physical Chemistry; vol. 99; nb. 13; (1995); p. 4525 - 4530, View in Reaxys

Degree of depolarization of Raman bands

Giorgini, M. G.; Foggi, P.; Cataliotti, R. S.; Distefano, M. R.; Moressi, A.; Mariani, L.; Journal of Chemical Physics; vol. 102; nb. 22; (1995); p. 8763 - 8772, View in Reaxys

Spectrum

neat (no solvent, solid phase)

Chen, Sheah; Tolbert, William A.; Dlott, Dana D.; Journal of Physical Chemistry; vol. 98; nb. 32; (1994); p. 7759 - 7766, View in Reaxys; Cavagnat, D.; Brom, H.; Nugteren, P. R.; Journal of Chemical Physics; vol. 87; nb. 2; (1987); p. 801 - 808, View in Reaxys

Bands

neat (no solvent, gas phase)

Phillips, David L.; Myers, Anne B.; Journal of Physical Chemistry; vol. 95; nb. 19; (1991); p. 7164 - 7171, View in Reaxys; Cataliotti, R. S.; Distefano, M. R.; Mariani, L.; Morresi, A.; Paliani, G.; et al.; Berichte der Bunsen-Gesellschaft; vol. 98; nb. 12; (1994); p. 1613 1618, View in Reaxys

Spectrum

neat (no solvent, gas phase)

Phillips, David L.; Myers, Anne B.; Journal of Physical Chemistry; vol. 95; nb. 19; (1991); p. 7164 - 7171, View in Reaxys; Cataliotti, R. S.; Paliani, G.; Mariani, L.; Santini, S.; Giorgini, M. G.; Journal of Physical Chemistry; vol. 96; nb. 7; (1992); p. 2961 - 2964, View in Reaxys; Gorse, Dominique; Cavagnat, Dominique; Pesquer, Michel; Lapouge, Christine; Journal of Physical Chemistry; vol. 97; nb. 17; (1993); p. 4262 - 4269, View in Reaxys

Spectrum

CCl4

Cataliotti, R. S.; Paliani, G.; Mariani, L.; Santini, S.; Giorgini, M. G.; Journal of Physical Chemistry; vol. 96; nb. 7; (1992); p. 2961 2964, View in Reaxys

Bands

CCl4

Cataliotti, R. S.; Paliani, G.; Mariani, L.; Santini, S.; Giorgini, M. G.; Journal of Physical Chemistry; vol. 96; nb. 7; (1992); p. 2961 2964, View in Reaxys

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Spectrum

H2O

Phillips, David L.; Myers, Anne B.; Journal of Physical Chemistry; vol. 95; nb. 19; (1991); p. 7164 - 7171, View in Reaxys

Spectrum

cyclohexane

Phillips, David L.; Myers, Anne B.; Journal of Physical Chemistry; vol. 95; nb. 19; (1991); p. 7164 - 7171, View in Reaxys

Spectrum

acetonitrile

Phillips, David L.; Myers, Anne B.; Journal of Physical Chemistry; vol. 95; nb. 19; (1991); p. 7164 - 7171, View in Reaxys

Bands

H2O

Phillips, David L.; Myers, Anne B.; Journal of Physical Chemistry; vol. 95; nb. 19; (1991); p. 7164 - 7171, View in Reaxys

Bands

cyclohexane

Phillips, David L.; Myers, Anne B.; Journal of Physical Chemistry; vol. 95; nb. 19; (1991); p. 7164 - 7171, View in Reaxys

Bands

acetonitrile

Phillips, David L.; Myers, Anne B.; Journal of Physical Chemistry; vol. 95; nb. 19; (1991); p. 7164 - 7171, View in Reaxys

Bands

Perekalin; Tetrahedron, Supplement; vol. 6; (1964); p. 135,140; Chem.Abstr.; nb. 14686; (1965), View in Reaxys; Buyan et al.; Optics and Spectroscopy; vol. 27; (1969); p. 132; ; p. 248, View in Reaxys; Kondilenko et al.; Optics and Spectroscopy; vol. 28; (1970); p. 367; ; p. 680, View in Reaxys; Cromer, Don T.; Ryan, Robert R.; Schiferl, David; Journal of Physical Chemistry; vol. 89; nb. 11; (1985); p. 2315 - 2318, View in Reaxys

Raman

Bobovich; Perekalin; Journal of Structural Chemistry; vol. 1; (1960); p. 288,289; Zhurnal Strukturnoi Khimii; vol. 1; (1960); p. 313, View in Reaxys; Lippincott; et al.; Spectrochimica Acta; vol. 22; (1966); p. 1493,1495, View in Reaxys; Fini; Mirone; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 32; (1976); p. 625,626, View in Reaxys; Kondilenko et al.; Optics and Spectroscopy; vol. 32; (1972); p. 337; ; p. 630, View in Reaxys; Kondilenko et al.; Optics and Spectroscopy; vol. 29; (1970); p. 572; ; p. 1070, View in Reaxys; Arndt; Yarwood; Chemical Physics Letters; vol. 45; (1977); p. 155, View in Reaxys; Kondilenko et al.; Optics and Spectroscopy; vol. 34; (1973); p. 716; ; p. 1230, View in Reaxys; Levin et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 20; (1971); p. 2442; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 20; (1971); p. 2575, View in Reaxys; Boldeskul et al.; Optics and Spectroscopy; vol. 37; (1974); p. 521; ; p. 912, View in Reaxys

Spectrum

in Tetrachlormethan

Behringer; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 62; (1958); p. 544,559, View in Reaxys

Bands

NO2-Streckschwingungsbanden (Loesung in Aceton)

Bobowitsch; Perekalin; Doklady Akademii Nauk SSSR; vol. 121; (1958); p. 1028; Doklady Chemistry; 118-123<1958>629, View in Reaxys

Spectrum

der Fluessigkeit

Smith et al.; Journal of Chemical Physics; vol. 18; (1950); p. 706,707,712, View in Reaxys

Degree of depolarization of Raman bands

der Fluessigkeit.

Smith et al.; Journal of Chemical Physics; vol. 18; (1950); p. 706,707,712, View in Reaxys

Spectrum

des Gemisches mit Methanol

Dadeiu; Kohlrausch; Phys.Z.; vol. 31; (1930); p. 517, View in Reaxys

Luminescence Spectroscopy (3) Description (LuReferences minescence Spectroscopy) Emission spectrum in the infrared region

Lipovskii; Sverdlov; Finkel'; Journal of applied spectroscopy; vol. 30; nb. 4; (1979); p. 464 - 467, View in Reaxys; Ruoff, Rodney S.; Kulp, Thomas J.; McDonald, J. D.; Journal of Chemical Physics; vol. 81; nb. 10; (1984); p. 4414 - 4420, View in Reaxys

Lasing properties

Lipovskii et al.; Sov. Phys. J. (Engl. Transl.); vol. 22; nb. 3; (1979); p. 50,264, View in Reaxys

Luminescence

Ambartzumian et al.; Chemical Physics Letters; vol. 36; (1975); p. 301,302-303, View in Reaxys

Fluorescence Spectroscopy (4)

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Description (Fluo- Solvent (Fluoresrescence Speccence Spectrotroscopy) scopy)

Comment (Fluorescence Spectroscopy)

References

Spectrum

350 - 700 nm

Gruzdkov, Yuri A.; Gupta, Yogendra M.; Journal of Physical Chemistry A; vol. 102; nb. 43; (1998); p. 8325 - 8332, View in Reaxys

neat (no solvent)

Fluorescence quenching

Tucker, Sheryl A.; Acree, William E.; Tanga, Mary J.; Tokita, Sumio; Hiruta, Kimihiro; Langhals, Heinz; Applied Spectroscopy; vol. 46; nb. 2; (1992); p. 229 - 235, View in Reaxys

Spectrum

340 - 900 nm

Butler, L. J.; Krajnovich, D.; Lee, Y. T.; Ondrey, G.; Bersohn, R.; Journal of Chemical Physics; vol. 79; nb. 4; (1983); p. 1708 - 1722, View in Reaxys

Fluorescence

Marciniak et al.; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 27; (1979); p. 853,854,857, View in Reaxys

Phosphorescence Spectroscopy (1) Description References (Phosphorescence Spectroscopy) Phosphorescence Marciniak et al.; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 27; (1979); p. 853,854,857, View in Reaxys Other Spectroscopic Methods (1) Description (Oth- References er Spectroscopic Methods) Photoelectron spectrum

Rao; Indian Journal of Chemistry; vol. 13; (1975); p. 950, View in Reaxys; Rabalais; Journal of Chemical Physics; vol. 57; (1972); p. 960, View in Reaxys; Kobayashi; Nagakura; Chemistry Letters; (1972); p. 903,904, View in Reaxys; Egdell et al.; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 72; (1976); p. 988,989, 991, View in Reaxys; Fujikawa et al.; Chemical Physics Letters; vol. 28; (1974); p. 433, View in Reaxys; Rao; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 14; (1976); p. 147, View in Reaxys; Qian, Kuangnan; Shukla, Anil; Futrell, Jean; Journal of the American Chemical Society; vol. 113; nb. 19; (1991); p. 7121 - 7129, View in Reaxys; Gilman, Jerome P.; Hsieh, Tacheng; Meisels, G. G.; Journal of Chemical Physics; vol. 78; nb. 3; (1983); p. 1174 - 1179, View in Reaxys

Pharmacological Data (45) 1 of 45

Comment (Pharmacological Data)

Bioactivities present

Patent; Zambon Group S.p.A.; US6358973; (2002); (B1) English, View in Reaxys; Patent; Eli Lilly and Company; US6358981; (2002); (B1) English, View in Reaxys; Brown,R.F.C. et al.; Australian Journal of Chemistry; vol. 20; (1967); p. 339 - 347, View in Reaxys; Patent; Kissei Pharmaceutical Co., Ltd.; EP1174421; (2002); (A1) English, View in Reaxys; Crow,W.D.; Gosney,I.; Australian Journal of Chemistry; vol. 22; (1969); p. 765 - 774, View in Reaxys; Hoskinson,R.M.; Australian Journal of Chemistry; vol. 23; (1970); p. 399 - 402, View in Reaxys; Happer,D.A.R.; Australian Journal of Chemistry; vol. 29; (1976); p. 2607 - 2614, View in Reaxys; Druey,J. et al.; Helvetica Chimica Acta; vol. 45; (1962); p. 600 - 610, View in Reaxys; Brossi; van Burik; Teitel; Helvetica chimica acta; vol. 51; nb. 8; (1968); p. 1965 - 1979, View in Reaxys; Wilhelm; Schmidt; Helvetica chimica acta; vol. 52; nb. 6; (1969); p. 1385 - 1395, View in Reaxys; Brossi,A.; Teitel,S.; Helvetica Chimica Acta; vol. 53; (1970); p. 1779 1787, View in Reaxys; Schlossarczyk,H. et al.; Helvetica Chimica Acta; vol. 56; (1973); p. 875 - 944, View in Reaxys; Kump; Bickel; Helvetica Chimica Acta; vol. 56; nb. 7; (1973); p. 2348 - 2377, View in Reaxys; Kienzle; Minder; Helvetica Chimica Acta; vol. 59; nb. 2; (1976); p. 439 - 452, View in Reaxys; Gosteli; Helvetica Chimica Acta; vol. 60; nb. 6; (1977); p. 1980 - 1983, View in Reaxys; Seebach,D.; Lehr,F.; Helvetica Chimica Acta; vol. 62; (1979); p. 2239 - 2257, View in Reaxys; Lehr,F. et al.; Helvetica Chimica Acta; vol. 62; (1979); p. 2258 2275, View in Reaxys; Mnatsakanyan,V.A. et al.; Collection of Czechoslovak Chemical Communications; vol. 42; (1977); p. 1421 - 1430, View in Reaxys; Kada,R.; Kovac,J.; Collection of Czechoslovak Chemical Communications; vol. 43; (1978); p. 2037 - 2040, View in Reaxys; Riemschneider,R. et al.; Monatshefte fuer Chemie; vol. 91; (1960); p. 630 - 638, View in Reaxys; Guth,V. et al.; Monatshefte fuer Chemie; vol. 94; (1963); p. 1262 - 1270, View in Reaxys; Klager,K.; Monatshefte fuer Chemie; vol. 96; (1965); p. 1 - 8, View in Reaxys; Weidmann,H. et al.; Monatshefte fuer Chemie; vol. 103; (1972); p. 883 - 888, View in Reaxys; Berner; Schulz; Reinshagen; ; vol. 108; nb. 1; (1977); p. 233 - 242, View in Reaxys; Berner; Schulz; Fischer; Reinshagen; ; vol. 109; nb. 3; (1978); p. 557 - 566, View in Reaxys; Tomita,M. et al.; Chemical and Pharmaceutical Bulletin; vol. 11; (1963); p. 1484 - 1490, View in Reaxys; Bessho,K.; Chemical and Pharmaceutical Bulletin; vol. 11; (1963); p. 1491 - 1494, View in Reaxys; Bessho,K.; Chemical and Pharmaceutical Bulletin; vol. 11; (1963); p. 1495 - 1499, View in Reaxys; Bessho,K.; Chemical and Pharmaceutical Bulletin; vol. 11; (1963); p. 1500 - 1503, View in Reaxys; Koizumi,J. et al.; Chemical and Pharmaceutical Bulletin; vol. 12; nb. 6; (1964); p. 696 - 705, View in Reaxys; Minami,S.; Uyeo,S.; Chemical and Pharmaceutical Bulletin; vol. 12; (1964); p. 1012 - 1020, View in Reaxys; Nambara,T. et al.; Chemical and

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Pharmaceutical Bulletin; vol. 19; (1971); p. 1137 - 1143, View in Reaxys; Fujita,E. et al.; Chemical and Pharmaceutical Bulletin; vol. 20; (1972); p. 368 - 379, View in Reaxys; Sone; Tominaga; Natsuki; et al.; Chemical and Pharmaceutical Bulletin; vol. 21; nb. 8; (1973); p. 1667 - 1675, View in Reaxys; Nagata; Okada; Itazaki; Uyeo; Chemical and Pharmaceutical Bulletin; vol. 23; nb. 11; (1975); p. 2878 - 2890, View in Reaxys; Tominaga,Y. et al.; Chemical and Pharmaceutical Bulletin; vol. 24; (1976); p. 1671 - 1675, View in Reaxys; Kametani; Satoh; Fukumoto; Chemical and Pharmaceutical Bulletin; vol. 25; nb. 5; (1977); p. 1129 - 1134, View in Reaxys; Kobayashi; Kihara; Shizu; Katayama; Ikeda; Kitahiro; Matsumoto; Chemical and Pharmaceutical Bulletin; vol. 25; nb. 12; (1977); p. 3312 3323, View in Reaxys; Kihara; Kobayashi; Chemical and Pharmaceutical Bulletin; vol. 26; nb. 1; (1978); p. 155 160, View in Reaxys; Kitagawa; Yoshikawa; Kadota; Chemical and Pharmaceutical Bulletin; vol. 26; nb. 2; (1978); p. 484 - 496, View in Reaxys; Sasaki,H. et al.; Chemical and Pharmaceutical Bulletin; vol. 26; (1978); p. 2111 2121, View in Reaxys; Takayama,H.; Okamoto,T.; Chemical and Pharmaceutical Bulletin; vol. 26; (1978); p. 2422 2427, View in Reaxys; Mizuyama; Tominaga; Matsuda; Kobayashi; Chemical and Pharmaceutical Bulletin; vol. 27; nb. 12; (1979); p. 2879 - 2889, View in Reaxys; Caramia,F.; Ricci,A.; Bollettino Chimico Farmaceutico; vol. 100; (1961); p. 93 - 103, View in Reaxys; Heacock,R.A. et al.; Canadian Journal of Chemistry; vol. 39; (1961); p. 1143 1147, View in Reaxys; Heacock,P.A.; Hutzinger,O.; Canadian Journal of Chemistry; vol. 41; (1963); p. 543 - 545, View in Reaxys; Currie,D.J. et al.; Canadian Journal of Chemistry; vol. 44; (1966); p. 1035 - 1043, View in Reaxys; Noland,W.E. et al.; Canadian Journal of Chemistry; vol. 45; (1967); p. 2969 - 2978, View in Reaxys; Wehrli,P.A. et al.; Canadian Journal of Chemistry; vol. 50; (1972); p. 3075 - 3079, View in Reaxys; Kovar,J.; Baer,H.H.; Canadian Journal of Chemistry; vol. 51; (1973); p. 1801 - 1811, View in Reaxys; Baer,H.H. et al.; Canadian Journal of Chemistry; vol. 51; (1973); p. 2843 - 2852, View in Reaxys; Perry,M.B.; Daoust,V.; Canadian Journal of Chemistry; vol. 51; (1973); p. 3039 - 3043, View in Reaxys; Butterick; Unrau; Canadian Journal of Chemistry; vol. 52; nb. 16; (1974); p. 2873 - 2879, View in Reaxys; Dime,D.; McLean,S.; Canadian Journal of Chemistry; vol. 57; (1979); p. 1569 - 1578, View in Reaxys; Zapior,B.; Sliwa,B.; Roczniki Chemii; vol. 39; (1965); p. 1461 - 1468, View in Reaxys; Richtarski,G. et al.; Roczniki Chemii; vol. 49; (1975); p. 2001 - 2004, View in Reaxys; Heusel,G.; Jung,G.; Liebigs Annalen der Chemie; (1979); p. 1173 - 1188, View in Reaxys; Kantlehner,W. et al.; Liebigs Annalen der Chemie; (1979); p. 2096 - 2113, View in Reaxys; Kroehnke,F.; Steuernagel,H.H.; Chemische Berichte; vol. 96; (1963); p. 494 - 497, View in Reaxys; Stetter,H.; Tacke,P.; Chemische Berichte; vol. 96; (1963); p. 694 - 698, View in Reaxys; Klages,F. et al.; Chemische Berichte; vol. 96; (1963); p. 2387 - 2393, View in Reaxys; Bredereck,H. et al.; Chemische Berichte; vol. 97; (1964); p. 3397 - 3406, View in Reaxys; Severin,T.; Brueck,B.; Chemische Berichte; vol. 98; (1965); p. 3847 - 3853, View in Reaxys; Dimroth,K.; Wache,H.; Chemische Berichte; vol. 99; (1966); p. 399 - 404, View in Reaxys; Dallacker,F.; Kern,J.; Chemische Berichte; vol. 99; (1966); p. 3830 - 3835, View in Reaxys; Gompper,R.; Schaefer,H.; Chemische Berichte; vol. 100; nb. 2; (1967); p. 591 - 604, View in Reaxys; Lichtenthaler,F.W.; Yahya,H.K.; Chemische Berichte; vol. 101; nb. 3; (1968); p. 908 - 915, View in Reaxys; Lichtenthaler,F.W. et al.; Chemische Berichte; vol. 101; (1968); p. 1819 - 1836, View in Reaxys; Lichtenthaler,F.W. et al.; Chemische Berichte; vol. 101; (1968); p. 1837 - 1845, View in Reaxys; Dimroth,K. et al.; Chemische Berichte; vol. 101; nb. 6; (1968); p. 2215 - 2223, View in Reaxys; Fischer,M. et al.; Chemische Berichte; vol. 101; (1968); p. 3313 - 3325, View in Reaxys; Bredereck,H. et al.; Chemische Berichte; vol. 104; (1971); p. 3475 - 3485, View in Reaxys; Huisgen,R.; Christl,M.; Chemische Berichte; vol. 106; (1973); p. 3291 - 3311, View in Reaxys; Tschesche; Spilles; Eckhardt; Chemische Berichte; vol. 107; nb. 2; (1974); p. 686 - 697, View in Reaxys; Eberlein; Heider; Machleidt; Chemische Berichte; vol. 107; nb. 4; (1974); p. 1275 - 1284, View in Reaxys; Seebach,D. et al.; Chemische Berichte; vol. 108; (1975); p. 1924 - 1945, View in Reaxys; Dimroth,K. et al.; Chemische Berichte; vol. 111; (1978); p. 264 - 271, View in Reaxys; Severin,T.; Ipach,I.; Chemische Berichte; vol. 111; (1978); p. 692 - 697, View in Reaxys; Seebach,D. et al.; Chemische Berichte; vol. 112; (1979); p. 234 - 248, View in Reaxys; Porotikova,V.A. et al.; Chemistry of Heterocyclic Compounds (New York, NY, United States); vol. 6; (1970); p. 1011 - 1013; Khimiya Geterotsiklicheskikh Soedinenii; vol. 6; nb. 8; (1970); p. 1083 - 1085, View in Reaxys; Marchenko,N.B. et al.; Chemistry of Heterocyclic Compounds (New York, NY, United States); vol. 12; (1976); p. 559 - 562; Khimiya Geterotsiklicheskikh Soedinenii; vol. 12; (1976); p. 665 - 668, View in Reaxys; Sowden,J.C.; Strobach,D.R.; Journal of the American Chemical Society; vol. 82; (1960); p. 956 - 958, View in Reaxys; Stork,G. et al.; Journal of the American Chemical Society; vol. 82; (1960); p. 4315 - 4323, View in Reaxys; Daly,J. et al.; Journal of the American Chemical Society; vol. 83; (1961); p. 4787 - 4792, View in Reaxys; Finkbeiner,H.L.; Stiles,M.; Journal of the American Chemical Society; vol. 85; (1963); p. 616 - 622, View in Reaxys; Taft,R.W. et al.; Journal of the American Chemical Society; vol. 85; (1963); p. 709 - 724, View in Reaxys; Epstein,J. et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 3075 - 3084, View in Reaxys; Klebe,J.F.; Journal of the American Chemical Society; vol. 86; (1964); p. 3399 - 3400, View in Reaxys; Haake,P. et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 3577 3578, View in Reaxys; Corey; Andersen; Carlson; Paust; Vedejs; Vlattas; Winter; Journal of the American Chemical Society; vol. 90; nb. 12; (1968); p. 3245 - 3247, View in Reaxys; Olah,G.A.; DeMember,J.R.; Journal of the American Chemical Society; vol. 92; (1970); p. 2562 - 2564, View in Reaxys; Gutsche,C.D. et al.; Journal of the American Chemical Society; vol. 93; nb. 20; (1971); p. 5172 - 5180, View in Reaxys; Russell,G.A. et al.; Journal of the American Chemical Society; vol. 94; (1972); p. 4959 - 4963, View in Reaxys; Cox,B.G.; Parker,A.J.; Journal of the American Chemical Society; vol. 95; (1973); p. 408 - 410, View in Reaxys; Bordwell,F.G. et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 7160 - 7162, View in Reaxys; Patent; Nippon Shinyaku Co. Ltd.; US5360822; (1994); (A1) English, View in Reaxys; Padwa,A.; Ku,A.; Journal of the American Chemical Society; vol. 100; (1978); p. 2181 - 2190, View in Reaxys; Yoshida; Matsuda; Okano; Kitani; Otsuka; ; vol. 101; nb. 8; (1979); p. 2027 - 2038, View in Reaxys; Russell,G.A.; Metcalfe,A.R.; Journal of the American Chemical Society; vol. 101; nb. 9; (1979); p. 2359 - 2362, View in Reaxys; Foehlisch,B. et al.; Justus Liebigs Annalen der Chemie; (1973); p. 1839 - 1850, View in Reaxys; Foehlisch,B. et al.; Justus Liebigs Annalen der Chemie; (1973); p. 1861 1881, View in Reaxys; Grundmann,C. et al.; Justus Liebigs Annalen der Chemie; (1975); p. 1029 - 1050, View in Reaxys; Bestmann,H.J. et al.; Justus Liebigs Annalen der Chemie; (1977); p. 276 - 281, View in Reaxys; Stetter,H.; Lennartz,J.; Justus Liebigs Annalen der Chemie; (1977); p. 1807 - 1816, View in Reaxys; Hellmann,H.; Elser,W.; Justus Liebigs Annalen der Chemie; vol. 639; (1961); p. 77 - 88, View in Reaxys; Meerwein,H. et al.; Jus-

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nb. 50; (2015); p. 15628 - 15631, View in Reaxys; Lu, Shuanglong; Peng, Jie; Wu, Junjie; Li, Chao; Cao, Xueqin; Gu, Hongwei; Chemical Communications; vol. 52; nb. 4; (2016); p. 760 - 763, View in Reaxys; Collier, Virginia E.; Ellebracht, Nathan C.; Lindy, George I.; Moschetta, Eric G.; Jones, Christopher W.; ACS Catalysis; vol. 6; nb. 1; (2016); p. 460 - 468, View in Reaxys; Patent; Council of Scientific and Industrial Research; KURESHY, Rukhsana Ilyas; KHAN, Noor-Ul-Hasan; ABDI, Sayed Hasan Razi; BAJAJ, Hari Chand; ROY, Tamal; DAS, Anjan; US2015/368181; (2015); (A1) English, View in Reaxys; Hayashi, Yujiro; Sakamoto, Daisuke; Okamura, Daichi; Organic Letters; vol. 18; nb. 1; (2016); p. 4 - 7, View in Reaxys; Ghosh, Priya; Deka, Manash J.; Saikia, Anil K.; Tetrahedron; vol. 72; nb. 5; (2016); p. 690 - 698, View in Reaxys; Marc, Patricia; Lynch, James; Blacker, A. John; Williams, Jonathan M. 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Chem.; (2015), View in Reaxys; Romo-Prez, Adriana; Miranda, Luis D.; Garca, Abraham; Tetrahedron Letters; vol. 56; nb. 48; (2015); p. 6669 - 6673, View in Reaxys; Li, Yifei; Feng, Chengjie; Shi, Hui; Xu, Xianxiu; Organic Letters; vol. 18; nb. 2; (2016); p. 324 - 327, View in Reaxys; De Assis, Francisco F.; Ferreira, Marco A. B.; Brocksom, Timothy J.; De Oliveira, Kleber T.; Organic and Biomolecular Chemistry; vol. 14; nb. 4; (2016); p. 1402 1412, View in Reaxys; Lin, Chia-Hsin; Hong, Bor-Cherng; Lee, Gene-Hsiang; RSC Advances; vol. 6; nb. 10; (2016); p. 8243 - 8247, View in Reaxys; Andrs, Jos M.; De La Cruz, Noelia; Valle, Mara; Pedrosa, Rafael; ChemPlusChem; vol. 81; nb. 1; (2016); p. 86 - 92, View in Reaxys; Devamani, Titu; Rauwerdink, Alissa M.; Lunzer, Mark; Jones, Bryan J.; Mooney, Joanna L.; Tan, Maxilmilien Alaric O.; Zhang, Zhi-Jun; Xu, Jian-He; Dean, Antony M.; Kazlauskas, Romas J.; Journal of the American Chemical Society; vol. 138; nb. 3; (2016); p. 1046 1056, View in Reaxys; Theppawong, Atiruj; Ploypradith, Poonsakdi; Chuawong, Pitak; Ruchirawat, Somsak; Chittchang, Montakarn; Chemistry - An Asian Journal; vol. 10; nb. 12; (2015); p. 2631 - 2650, View in Reaxys; Zhang, Wen-Qiang; Li, Qiu-Yan; Zhang, Quan; Lu, Yingqiao; Lu, Han; Wang, Wenguang; Zhao, Xinsheng; Wang, Xiao-Jun; Inorganic Chemistry; vol. 55; nb. 3; (2016); p. 1005 - 1007, View in Reaxys; Patent; GRÜNENTHAL GMBH; WEGERT, Anita; KÜHNERT, Sven; KOENIGS, René, Michael; NOLTE, Bert; LINZ, Klaus; HARLFINGER, Stephanie; KÖGEL, Babette-Yvonne; RATCLIFFE, Paul; THEIL, Fritz; GRÖGER, Olga; BRAUN, Birgit; (223 pag.); WO2016/8582; (2016); (A1) English, View in Reaxys; Marset, Xavier; Prez, Juana M.; Ramn, Diego J.; Green Chemistry; vol. 18; nb. 3; (2016); p. 826 - 833, View in Reaxys; Perez, Vincent; Rabasso, Nicolas; Fadel, Antoine; European Journal of Organic Chemistry; vol. 2016; nb. 2; (2016); p. 320 - 324, View in Reaxys; Yan, Yizhe; Niu, Bin; Xu, Kun; Yu, Jianhua; Zhi, Huanhuan; Liu, Yanqi; Advanced Synthesis and Catalysis; vol. 358; nb. 2; (2016); p. 212 - 217, View in Reaxys; Patent; Boehringer Ingelheim International GmbH; BRENNEMAN, Jehrod Burnett; GINN, John David; HOPKINS, Tamara Denise; LOWE, MIchael D.; SARKO, Christopher Ronald; WESTBROOK, John A.; YU, Maolin; ZHANG, Zhonghua; (233 pag.); US2016/24059; (2016); (A1) English, View in Reaxys; Samzadeh-Kermani, Alireza; Journal of Sulfur Chemistry; vol. 37; nb. 1; (2016); p. 105 - 113, View in Reaxys; Grigorjeva, Jeena; Uzulea, Jevgeija; Rjabovs, Vitalijs; Turks, Maris; Chemistry of Heterocyclic Compounds; vol. 51; nb. 10; (2015); p. 883 - 890; Khim. Geterotsikl. Soedin.; vol. 51; nb. 10; (2015); p. 883 - 890,8, View in Reaxys; Dudina; Berezin; Semeikin; Antina; Russian Journal of General Chemistry; vol. 85; nb. 12; (2015); p. 2739 - 2742; Zh. Obshch. Khim.; vol. 85; nb. 12; (2015); p. 2007 - 2010,4, View in Reaxys; Lai, Holden W.H.; Wiscons, Ren A.; Zentner, Cassandra A.; Zeller, Matthias; Rowsell, Jesse L.C.; Crystal Growth and Design; vol. 16; nb. 2; (2016); p. 821 - 833, View in Reaxys; More, Atul A.; Ramana, Chepuri V.; Organic Letters; vol. 18; nb. 3; (2016); p. 612 - 615, View in Reaxys; Pan; Zhang; Wang; Xia; Molecular Crystals and Liquid Crystals; vol. 624; nb. 1; (2016); p. 251 - 256, View in Reaxys; Pang, Lanfang; Zhou, Yanmei; Wang, Enze; Yu, Fang; Zhou, Hua; Gao, Wenli; RSC Advances; vol. 6; nb. 20; (2016); p. 16467 - 16473, View in Reaxys; Zhang, Mo; Lu, Jun; Zhang, Jia-Nan; Zhang, Zhan-Hui; Catalysis Communications; vol. 78; (2016); p. 26 - 32, View in Reaxys; Keithellakpam, Sanjoy; Laitonjam, Warjeet S.; Indian Journal of Chemistry - Section B Organic and Medicinal

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Chemistry; vol. 55B; nb. 1; (2016); p. 110 - 113, View in Reaxys; Xiao, Jian; Wen, Hao; Wang, Liang; Xu, Lubin; Hao, Zhihui; Shao, Chang-Lun; Wang, Chang-Yun; Green Chemistry; vol. 18; nb. 4; (2016); p. 1032 - 1037, View in Reaxys; Ziganshin, Marat A.; Ziganshina, Sufia A.; Gubina, Nadezhda S.; Gerasimov, Alexander V.; Gorbatchuk, Valery V.; Bukharaev, Anastas A.; Oriental Journal of Chemistry; vol. 31; nb. 4; (2015); p. 1977 1984, View in Reaxys; Chen, Haifeng; Han, Xinya; Qin, Nian; Wei, Lin; Yang, Yue; Rao, Li; Chi, Bo; Feng, Lingling; Ren, Yanliang; Wan, Jian; Bioorganic and Medicinal Chemistry; vol. 24; nb. 6; (2016); p. 1225 - 1230, View in Reaxys; Ma, Xiao-Dong; Qiu, Ni; Yang, Bo; He, Qiao-Jun; Hu, Yong-Zhou; MedChemComm; vol. 7; nb. 2; (2016); p. 297 - 310, View in Reaxys; Jensen, Mikkel T.; Juhl, Martin; Nielsen, Dennis U.; Jacobsen, Mikkel F.; Lindhardt, Anders T.; Skrydstrup, Troels; Journal of Organic Chemistry; vol. 81; nb. 4; (2016); p. 1358 - 1366, View in Reaxys; Jiao, Tangqian; Tu, Jingxuan; Li, Gaoqiang; Xu, Feng; Journal of Molecular Catalysis A: Chemical; vol. 416; (2016); p. 56 - 62, View in Reaxys; Sarma, Manas Jyoti; Phukan, Prodeep; Synthetic Communications; vol. 46; nb. 3; (2016); p. 257 - 262, View in Reaxys; Shimkin, Kirk W.; Gildner, Peter G.; Watson, Donald A.; Organic Letters; vol. 18; nb. 5; (2016); p. 988 - 991, View in Reaxys; Quan, Ying; Li, Qiu-Yan; Zhang, Quan; Zhang, Wen-Qiang; Lu, Han; Yu, Jun-Hao; Chen, Jian; Zhao, Xinsheng; Wang, Xiao-Jun; RSC Advances; vol. 6; nb. 29; (2016); p. 23995 - 23999, View in Reaxys; Patent; CTXT PTY LTD; BERGMAN, Ylva Elisabet; FOITZIK, Richard Charles; MORROW, Benjamin Joseph; CAMERINO, Michelle Ang; WALKER, Scott Raymond; LAGIAKOS, H. Rachel; FEUTRILL, John; STEVENSON, Graeme Irvine; STUPPLE, Paul Anthony; (222 pag.); WO2016/34673; (2016); (A1) English, View in Reaxys 2 of 45

Effect (Pharmacological Data)

antibacterial

Species or Test-System (Pharmacological Data)

Escherichia coli ATCC 25922

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Method (Pharmacological Data)

name of assay/method: broth microdilution assay

Further Details (Pharmacological Data)

minimal inhibitory concentration (MIC)

Type (Pharmacological Data)

MIC

Value of Type (Pharmacological Data)

32 μg/ml

Scholz, Therese; Heyl, Carina L.; Bernardi, Dan; Zimmermann, Stefan; Kattner, Lars; Klein, Christian D.; Bioorganic and Medicinal Chemistry; vol. 21; nb. 3; (2013); p. 795 - 804, View in Reaxys 3 of 45

Effect (Pharmacological Data)

antibacterial

Species or Test-System (Pharmacological Data)

Pseudomonas aeruginosa ATCC 27853

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Method (Pharmacological Data)

name of assay/method: broth microdilution assay

Further Details (Pharmacological Data)

minimal inhibitory concentration (MIC)

Type (Pharmacological Data)

MIC

Value of Type (Pharmacological Data)

8 μg/ml

Effect (Pharmacological Data)

antibacterial

Species or Test-System (Pharmacological Data)

Staphylococcus aureus ATCC 25923

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

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Method (Pharmacological Data)

name of assay/method: broth microdilution assay

Further Details (Pharmacological Data)

minimal inhibitory concentration (MIC)

Type (Pharmacological Data)

MIC

Value of Type (Pharmacological Data)

8 μg/ml

Effect (Pharmacological Data)

antibacterial

Species or Test-System (Pharmacological Data)

Staphylococcus aureus NCTC 27853; pre-existing medical conditions: methicillin-resistant

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Method (Pharmacological Data)

name of assay/method: broth microdilution assay

Further Details (Pharmacological Data)

minimal inhibitory concentration (MIC)

Type (Pharmacological Data)

MIC

Value of Type (Pharmacological Data)

> 32 μg/ml

Effect (Pharmacological Data)

cytotoxic

Species or Test-System (Pharmacological Data)

cervical carcinoma CaSki cells of human

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Type (Pharmacological Data)

IC50

Value of Type (Pharmacological Data)

>= 100 μmol/l

Effect (Pharmacological Data)

cytotoxic

Species or Test-System (Pharmacological Data)

colon carcinoma SW-707 cells of human

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Type (Pharmacological Data)

IC50

Value of Type (Pharmacological Data)

>= 100 μmol/l

Effect (Pharmacological Data)

cytotoxic

398/412

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Species or Test-System (Pharmacological Data)

diploid embryonic lung fibroblast flow 2002 cells of human

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Type (Pharmacological Data)

IC50

Value of Type (Pharmacological Data)

>= 100 μmol/l

Effect (Pharmacological Data)

cytotoxic

Species or Test-System (Pharmacological Data)

lung adenocarcinoma Calu-6 cells of human

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Type (Pharmacological Data)

IC50

Value of Type (Pharmacological Data)

>= 100 μmol/l

Effect (Pharmacological Data)

cytotoxic

Species or Test-System (Pharmacological Data)

pancreas adenocarcinoma Capan-1 cells of human

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Type (Pharmacological Data)

IC50

Value of Type (Pharmacological Data)

>= 100 μmol/l

Effect (Pharmacological Data)

cytotoxic

Species or Test-System (Pharmacological Data)

skin epidermoid carcinoma A-431 cells of human

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Type (Pharmacological Data)

IC50

Value of Type (Pharmacological Data)

>= 100 μmol/l

Effect (Pharmacological Data)

cytotoxic

Species or Test-System (Pharmacological Data)

skin keratinocyte HaCaT cells of human

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

399/412

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Type (Pharmacological Data)

IC50

Value of Type (Pharmacological Data)

>= 100 μmol/l

Effect (Pharmacological Data)

cytotoxic

Species or Test-System (Pharmacological Data)

skin melanoma MeWo cells of human

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Type (Pharmacological Data)

IC50

Value of Type (Pharmacological Data)

>= 100 μmol/l

Effect (Pharmacological Data)

enzyme activity; inhibition of

Species or Test-System (Pharmacological Data)

MetAP enzyme of Escherichia coli

Concentration (Pharmacological Data)

10 μmol/l

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Method (Pharmacological Data)

name of assay/method: MetAP assay

Results

molecular target: MetAP enzyme

Effect (Pharmacological Data)

enzyme activity; inhibition of

Species or Test-System (Pharmacological Data)

MetAP enzyme of Escherichia coli

Concentration (Pharmacological Data)

10 μmol/l

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Method (Pharmacological Data)

name of assay/method: MetAP assay

Results

no effect

Effect (Pharmacological Data)

enzyme activity; inhibition of

Species or Test-System (Pharmacological Data)

MurA enzyme C115D mutant of Escherichia coli

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Results

no effect

400/412

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Effect (Pharmacological Data)

enzyme activity; inhibition of

Species or Test-System (Pharmacological Data)

MurA enzyme of Escherichia coli

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Results

no effect

Effect (Pharmacological Data)

enzyme activity; inhibition of

Species or Test-System (Pharmacological Data)

MurA enzyme of Pseudomonas aeruginosa

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Results

no effect

Effect (Pharmacological Data)

enzyme activity; inhibition of

Species or Test-System (Pharmacological Data)

MurA2 enzyme of Staphylococcus aureus

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Results

molecular target: MurA2 enzyme

Effect (Pharmacological Data)

enzyme activity; inhibition of

Species or Test-System (Pharmacological Data)

MurA2 enzyme of Staphylococcus aureus

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Results

no effect

Effect (Pharmacological Data)

enzyme activity; inhibition of

Species or Test-System (Pharmacological Data)

NS2B-NS3 protease of Dengue virus

Concentration (Pharmacological Data)

50 μmol/l

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Method (Pharmacological Data)

name of assay/method: DV NS2B-NS3 assay

Results

molecular target: NS2B-NS3 protease

Scholz, Therese; Heyl, Carina L.; Bernardi, Dan; Zimmermann, Stefan; Kattner, Lars; Klein, Christian D.; Bioorganic and Medicinal Chemistry; vol. 21; nb. 3; (2013); p. 795 - 804, View in Reaxys

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22 of 45

Effect (Pharmacological Data)

enzyme activity; inhibition of

Species or Test-System (Pharmacological Data)

NS2B-NS3 protease of Dengue virus

Concentration (Pharmacological Data)

50 μmol/l

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Method (Pharmacological Data)

name of assay/method: DV NS2B-NS3 assay

Results

no effect

Effect (Pharmacological Data)

enzyme activity; inhibition of

Species or Test-System (Pharmacological Data)

methionine aminopeptidase MetAP 1 of human

Concentration (Pharmacological Data)

10 μmol/l

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Method (Pharmacological Data)

name of assay/method: MetAP assay

Results

no effect

Effect (Pharmacological Data)

enzyme activity; inhibition of

Species or Test-System (Pharmacological Data)

methionine aminopeptidase MetAP 2 of human

Concentration (Pharmacological Data)

10 μmol/l

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Method (Pharmacological Data)

name of assay/method: MetAP assay

Results

molecular target: methionine aminopeptidase MetAP 2; species of target: human

Effect (Pharmacological Data)

enzyme activity; inhibition of

Species or Test-System (Pharmacological Data)

methionine aminopeptidase MetAP 2 of human

Concentration (Pharmacological Data)

10 μmol/l

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Method (Pharmacological Data)

name of assay/method: MetAP assay

Results

no effect

Scholz, Therese; Heyl, Carina L.; Bernardi, Dan; Zimmermann, Stefan; Kattner, Lars; Klein, Christian D.; Bioorganic and Medicinal Chemistry; vol. 21; nb. 3; (2013); p. 795 - 804, View in Reaxys

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26 of 45

Effect (Pharmacological Data)

enzyme activity; inhibition of

Species or Test-System (Pharmacological Data)

thrombin

Concentration (Pharmacological Data)

25 μmol/l

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Method (Pharmacological Data)

name of assay/method: thrombin assay

Results

molecular target: thrombin

Effect (Pharmacological Data)

enzyme activity; inhibition of

Species or Test-System (Pharmacological Data)

thrombin

Concentration (Pharmacological Data)

25 μmol/l

Kind of Dosing (Pharmacological Data)

title comp. in DMSO

Method (Pharmacological Data)

name of assay/method: thrombin assay

Results

no effect

Effect (Pharmacological Data)

carcinogenicity

Species or Test-System (Pharmacological Data)

animal

Type (Pharmacological Data)

log TD50

Value of Type (Pharmacological Data)

0.179

Location

supporting information

Toropov; Toropova; Benfenati; European Journal of Medicinal Chemistry; vol. 45; nb. 9; (2010); p. 3581 - 3587, View in Reaxys 29 of 45

Effect (Pharmacological Data)

enzyme activity; inhibition of

Species or Test-System (Pharmacological Data)

hydroxynitrile lyase of Hevea brasiliensis

Further Details (Pharmacological Data)

inhibition constant during cleavage of 2-nitro-1-phenylethanol (Ki)

Type (Pharmacological Data)

Value of Type (Pharmacological Data)

103 mmol/l

Yuryev, Ruslan; Purkarthofer, Thomas; Gruber, Mandana; Griengl, Herfried; Liese, Andreas; Biocatalysis and Biotransformation; vol. 28; nb. 5-6; (2010); p. 348 - 356, View in Reaxys 30 of 45

Effect (Pharmacological Data)

enzyme activity; inhibition of

403/412

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Species or Test-System (Pharmacological Data)

hydroxynitrile lyase of Hevea brasiliensis

Further Details (Pharmacological Data)

inhibition constant during synthesis of 2-nitro-1-phenylethanol (Ki)

Type (Pharmacological Data)

Value of Type (Pharmacological Data)

64 mmol/l

Yuryev, Ruslan; Purkarthofer, Thomas; Gruber, Mandana; Griengl, Herfried; Liese, Andreas; Biocatalysis and Biotransformation; vol. 28; nb. 5-6; (2010); p. 348 - 356, View in Reaxys 31 of 45

Effect (Pharmacological Data)

enzyme activity; inhibition of

Species or Test-System (Pharmacological Data)

hydroxynitrile lyase of Hevea brasiliensis

Results

molecular target: hydroxynitrile lyase

Yuryev, Ruslan; Purkarthofer, Thomas; Gruber, Mandana; Griengl, Herfried; Liese, Andreas; Biocatalysis and Biotransformation; vol. 28; nb. 5-6; (2010); p. 348 - 356, View in Reaxys 32 of 45

Effect (Pharmacological Data)

insecticidal

Species or Test-System (Pharmacological Data)

cockroach

Method (Pharmacological Data)

In this embodiment, an aerosol pesticidal composition of the present disclosure was prepared. The ingredients and amounts used to prepare the composition are set forth in Table 15 below.

Results

proportion dead at 24 h (no unit) = 0-0.273 at 0.7-0.8 mg

Location

Page/Page column 15

Comment (Pharmacological Data)

potential area of application: agro

Patent; Whitmire Micro-Gen Research Laboratories, Inc.; US2009/257958; (2009); (A1) English, View in Reaxys 33 of 45

Effect (Pharmacological Data)

insecticidal

Species or Test-System (Pharmacological Data)

cockroach

Method (Pharmacological Data)

The composite data for certain compositions is presented below (Table 14), also including the calculated proportion of cockroaches dead at 24 hours for the group treated with alcohol alone and for the group treated with the composition comprising PD23 and alcohol. The difference between the proportion of dead cockroaches in the group treated with the composition comprising PD23 and alcohol and the group treated with alcohol alone was calculated, and is also presented in Table 14. Here, the increase in mortality indicates a synergistic effect with the combination compared to the alcohol or mineral oil alone, with a higher difference indicating a greater synergy. The straight chain saturated alcohols with chain lengths of C3-C7 demonstrated the greatest increase, or difference, in mortality when combined with PD23 mineral oil, as compared to the other alcohols tested.

Results

proportion dead at 24 h (no unit) = 0.179 at 0.8 mg

Location

Page/Page column 16; 17

Comment (Pharmacological Data)

potential area of application: agro

Patent; Whitmire Micro-Gen Research Laboratories, Inc.; US2009/257958; (2009); (A1) English, View in Reaxys 34 of 45

Effect (Pharmacological Data)

Pesticidal

Species or Test-System (Pharmacological Data)

Sclerotium rolfsii

404/412

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Method (Pharmacological Data)

Effect of Degradation Products of Bromopicrin on the Viability of Soil-Borne Fungi Materials and Experimental Methods: Nitromethane (NM) was purchased from Aldrich, Cat No. 10,817.0, lot. 535033-196. Bromonitromethane (BNM) was purchased from Aldrich, 90percent 255858. Dibromonitromethane (DBNM) was obtained from TAMI, 90percent, 38585-16-F-4. Bromopicrin (BP) was obtained from TAMI, BP-2006-2. HPLC analyses were performed using HP 1090 pumping system equipped with HP DAD 1090 UV detector operated at 220 nm and a C-18 Kromasil column, 250.x.4.6 mm, 100 A, 5 μm, using a mixture of 40percent H2O (pH adjusted to 2.5+/-0.2 with HClO4) and 60percent acetonitrile as the mobile phase, at a flow rate of 1 ml/minute. Standard solutions were prepared in acetonitrile at a working concentration of about 100 mg/liter. Degradation of Bromopicrin in Soil: 5 mg bromopicrin were applied to 1,000 grams of Rehovot sand soil (95percent sand). 0.5, 3 and 7 days post-application, samples of the treated soil were extracted and analyzed by HPLC and GC-MS, so as to identify the ingredients therein. The extraction procedure was effected by mixing 100 grams of the treated soil with 100 ml acetonitrile, for 30 minutes, followed by filtration. HPLC analysis was performed as described hereinabove. Retenetion times: NM=3.3 minutes; BNM=4.3 minutes; DBNM=5.7 minutes; BP=7.9 minutes FIG. 5 presents the data obtained in the above-described studies, and shows the dissipation of bromopicrin and generation of its derivatives, as degradation products thereof, during the first week following application of bromopicrin to soil. As shown in FIG. 5, bromopicrin rapidly dissipates in soil and degrades into lower bromonitromethane derivatives, such that dibromonitromethane is generated immediately and then dissipates to some extent, and monobromonitromethane is slowly yet consistently generated. Nitromethane is also generated during time, although to a much lesser extent. Without being bound to any particular theory, it is suggested that bromopicrin degrades mostly to dibromonitromethane, which, in turn, further degrades to produce monobromonitromethane. Effect of Bromopicrin and its Degradation Product on Soil-Borne Fungi: In preliminary studies conducted so as to evaluate the effect of these degradation products on the viability and growth of soil-borne pests, their effect on two types of soil-borne fungi was studied, using the same experimental protocols as described hereinabove, with the exception of studies conducted with Sclerotium rolfsii in which sclerotia were used. Viability of Sclerotium sclerotia was tested using the BromoCresol Green calorimetric method as follows: Sclerotium sclerotia that undergo germination secrete oxalic acid, which serves as a marker indicating their viability, by means of color change. When oxalic acid reacts with BromoCresol Green color change from blue to yellow is observed, indicating the amount of germinating sclerotia and hence their percent viability. Thus, bromopicrin (BP), dibromonitromethane (DBNM), bromonitromethane (BNM) and nitromethane (NM), were prepared and applied each separately at a concentration of 30 mg/Kg (ppm, w/w), to 1,000 grams of Rehovot soil inoculated with Fusarium oxysporum f. sp radicis-lycopersici (FORL) or S. rolfosii. FIG. 6 presents the data obtained in these studies as the percent survival values of the tested microorganisms, 7 days following application to soil, compared to non-treated soil as control, and clearly shows that both dibromonitromethane and monobromonitromethane are effective in controlling soil-borne fungi. It is further shown that nitromethane (NM) has no effect in controlling pests, as compared to the other degradation products.

Location

Page/Page column 9-10; sheet 5

Comment (Pharmacological Data)

potential area of application: agro; No effect

Patent; Bromine Compounds Ltd.; US2007/249501; (2007); (A1) English, View in Reaxys 35 of 45

Effect (Pharmacological Data)

Pesticidal

Species or Test-System (Pharmacological Data)

Fusarium oxysporum

Method (Pharmacological Data)

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for 30 minutes, followed by filtration. HPLC analysis was performed as described hereinabove. Retenetion times: NM=3.3 minutes; BNM=4.3 minutes; DBNM=5.7 minutes; BP=7.9 minutes FIG. 5 presents the data obtained in the above-described studies, and shows the dissipation of bromopicrin and generation of its derivatives, as degradation products thereof, during the first week following application of bromopicrin to soil. As shown in FIG. 5, bromopicrin rapidly dissipates in soil and degrades into lower bromonitromethane derivatives, such that dibromonitromethane is generated immediately and then dissipates to some extent, and monobromonitromethane is slowly yet consistently generated. Nitromethane is also generated during time, although to a much lesser extent. Without being bound to any particular theory, it is suggested that bromopicrin degrades mostly to dibromonitromethane, which, in turn, further degrades to produce monobromonitromethane. Effect of Bromopicrin and its Degradation Product on Soil-Borne Fungi: In preliminary studies conducted so as to evaluate the effect of these degradation products on the viability and growth of soil-borne pests, their effect on two types of soil-borne fungi was studied, using the same experimental protocols as described hereinabove, with the exception of studies conducted with Sclerotium rolfsii in which sclerotia were used. Viability of Sclerotium sclerotia was tested using the BromoCresol Green calorimetric method as follows: Sclerotium sclerotia that undergo germination secrete oxalic acid, which serves as a marker indicating their viability, by means of color change. When oxalic acid reacts with BromoCresol Green color change from blue to yellow is observed, indicating the amount of germinating sclerotia and hence their percent viability. Thus, bromopicrin (BP), dibromonitromethane (DBNM), bromonitromethane (BNM) and nitromethane (NM), were prepared and applied each separately at a concentration of 30 mg/Kg (ppm, w/w), to 1,000 grams of Rehovot soil inoculated with Fusarium oxysporum f. sp radicis-lycopersici (FORL) or S. rolfosii. FIG. 6 presents the data obtained in these studies as the percent survival values of the tested microorganisms, 7 days following application to soil, compared to non-treated soil as control, and clearly shows that both dibromonitromethane and monobromonitromethane are effective in controlling soil-borne fungi. It is further shown that nitromethane (NM) has no effect in controlling pests, as compared to the other degradation products. Location

Page/Page column 9-10; sheet 5

Comment (Pharmacological Data)

potential area of application: agro; No effect

Patent; Bromine Compounds Ltd.; US2007/249501; (2007); (A1) English, View in Reaxys 36 of 45

Effect (Pharmacological Data)

enzyme; inhib. of

Endpoint of Effect (Pharmacological Data)

PDH activity

Species or Test-System (Pharmacological Data)

porcine heart PDH complex

Concentration (Pharmacological Data)

<= 300 μmol/l

Kind of Dosing (Pharmacological Data)

title comp. was dissolved in DMSO

Exposure Period (Pharmacological Data)

30 min

Method (Pharmacological Data)

in vitro; PDH complex was depleted of the thiol and incub. with title comp. in phosph. buffer (pH 8.0) for 30 min at 25 deg C; PDH activity assay according to Brown and Perham

Further Details (Pharmacological Data)

PDH - pyruvate dehydrogenase; estimation of inhibitory effect of title comp. on PDH activity

Type (Pharmacological Data)

IC50

Value of Type (Pharmacological Data)

> 200 μmol/l

Sparks, Susan E.; Quistad, Gary B.; Li, Weiwei; Casida, John E.; Journal of Biochemical and Molecular Toxicology; vol. 14; nb. 1; (2000); p. 26 - 32, View in Reaxys 37 of 45

Effect (Pharmacological Data)

enzyme; inhib. of

Endpoint of Effect (Pharmacological Data)

SDH activity

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Species or Test-System (Pharmacological Data)

mouse liver SDH complex

Concentration (Pharmacological Data)

<= 300 μmol/l

Kind of Dosing (Pharmacological Data)

10, 30, 100, and 300 μmol/l, in DMSO

Exposure Period (Pharmacological Data)

5 min

Method (Pharmacological Data)

in vitro; SDH complex was incub. with title comp. in phosph. buffer (pH 7.4) for 5 min at 30 deg C; SDH activity was estimated by the method of Hatefi and Stiggall as modified by Gassner

Further Details (Pharmacological Data)

SDH - succinate dehydrogenase; estimation of inhibitory effect of title comp. on SDH activity; SDH (succinate:ubiquinone oxidoreductase, Complex II)

Type (Pharmacological Data)

IC50

Value of Type (Pharmacological Data)

> 200 μmol/l

Sparks, Susan E.; Quistad, Gary B.; Li, Weiwei; Casida, John E.; Journal of Biochemical and Molecular Toxicology; vol. 14; nb. 1; (2000); p. 26 - 32, View in Reaxys 38 of 45

Effect (Pharmacological Data)

genetic toxicity in vivo

Species or Test-System (Pharmacological Data)

B6C3F1 mouse

Sex

male

Route of Application

inhalation

Concentration (Pharmacological Data)

94 - 1500 ppm

Kind of Dosing (Pharmacological Data)

subchronic dosage; inhalation of title comp. for 6 hr/day, 5 day/wk for 90 days

Method (Pharmacological Data)

in vivo; 9-10 mice per group were treated with title comp.; blood collected and stained; MN frequencies (PCE and NCE) determined using ca. 1000 cells by epifluorescence microscopy

Further Details (Pharmacological Data)

PCE: polychromatic erythrocytes; NCE: normochromatic erythrocytes; MN: micronucleus; control: without title comp.; carcinogenicity studies conducted by the National Toxicology Program (NTP); dose: highest negative exposure level

Results

MN-NCE/1000 NCE: (dose, ppm): 0.52 (control), 0.80 (94), 0.61 (188), 0.67 (375), 0.64 (750), 0.70 (1500); percent PCE (dose, ppm): 1.04 (control), 1.25 (94), 1.21 (188), 1.21 (375), 1.30 (750), 1.46 (1500); dose: 1500 ppm; title comp.: carcinogenic

Witt, Kristine L.; Knapton, Alan; Wehr, Carol M.; Hook, Graham J.; Mirsalis, Jon; Shelby, Michael D.; MacGregor, James T.; Environmental and Molecular Mutagenesis; vol. 36; nb. 3; (2000); p. 163 - 194, View in Reaxys 39 of 45

Effect (Pharmacological Data)

genetic toxicity in vivo

Species or Test-System (Pharmacological Data)

B6C3F1 mouse

Sex

female

Route of Application

inhalation

Concentration (Pharmacological Data)

94 - 1500 ppm

Kind of Dosing (Pharmacological Data)

subchronic dosage; inhalation of title comp. for 6 hr/day, 5 day/wk for 90 days

Method (Pharmacological Data)

in vivo; 9-10 mice per group were treated with title comp.; blood collected and stained; MN frequencies (PCE and NCE) determined using ca. 1000 cells by epifluorescence microscopy

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Further Details (Pharmacological Data)

Results

MN-NCE/1000 NCE: (dose, ppm): 0.55 (control), 0.37 (94), 0.40 (188), 0.39 (375), 0.55 (750), 0.49 (1500); percent PCE (dose, ppm): 1.42 (control), 1.24 (94), 1.27 (188), 1.43 (375), 1.60 (750), 1.85 (1500); dose: 1500 ppm; title comp.: carcinogenic

Effect (Pharmacological Data)

mutagenic (microorganism)

Species or Test-System (Pharmacological Data)

Salmonella typhimurium TA 100

Concentration (Pharmacological Data)

50 - 1000 nmol/plate

Kind of Dosing (Pharmacological Data)

0.1 ml solut. of the title comp. in DMSO was added into preincubation medium

Exposure Period (Pharmacological Data)

20 min

Method (Pharmacological Data)

in vitro; Ames test (plate incorporation assay); preincubation method; at 37 deg C; with (+) or without (-) mouse liver microsomes and NADH; two-fold dilution series

Further Details (Pharmacological Data)

preincubation mixture: sodium phosphate buffer (0.5 ml, 100 mM, pH 7.4), 0.1 ml of overnight bacterial culture, title comp., mouse liver microsomes (0.64 mg protein), 1.5 mg NADH; GSH: glutathione

Comment (Pharmacological Data)

No effect

Schneider, Manfred; Quistad, Gary B.; Casida, John E.; Mutation Research - Genetic Toxicology and Environmental Mutagenesis; vol. 439; nb. 2; (1999); p. 233 - 238, View in Reaxys 41 of 45

Effect (Pharmacological Data)

mutagenic (microorganism)

Species or Test-System (Pharmacological Data)

Salmonella typhimurium TA 100

Concentration (Pharmacological Data)

50 - 1000 nmol/plate

Kind of Dosing (Pharmacological Data)

0.1 ml solut. of the title comp. in DMSO was added into preincubation medium

Exposure Period (Pharmacological Data)

20 min

Method (Pharmacological Data)

in vitro; Ames test (plate incorporation assay); preincubation method; at 37 deg C; with (+) or without (-) GSH activation; two-fold dilution series

Further Details (Pharmacological Data)

preincubation mixture: sodium phosphate buffer (0.5 ml, 100 mM, pH 7.4), 0.1 ml of overnight bacterial culture, title comp., 14 mM GSH (5 mM/plate); GSH: glutathione

Comment (Pharmacological Data)

No effect

Schneider, Manfred; Quistad, Gary B.; Casida, John E.; Mutation Research - Genetic Toxicology and Environmental Mutagenesis; vol. 439; nb. 2; (1999); p. 233 - 238, View in Reaxys 42 of 45

Effect (Pharmacological Data)

genetic toxicity in vitro

Species or Test-System (Pharmacological Data)

Syrian hamster embryo (SHE) cells

Concentration (Pharmacological Data)

5 - 6 mg/l

Exposure Period (Pharmacological Data)

24 h

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Method (Pharmacological Data)

micronucleus test performed; the percentage of binucleated cells ( percent BN)-500 cells analyzed and micronucleated cells ( percent MNBC)-1000 cells analyzed, determined

Further Details (Pharmacological Data)

relative cell number (number of live cells in treated/number of live cells in the solvent control*100) determined

Results

dose-dependent decrease of relative cell number and percent BN; percent MNBC: 2.8, 2.4 and 2.6 at the dose 5, 5.5 and 6 μg/ml, resp.

Gibson, David P.; Brauninger, Roger; Shaffi, Hussain S.; Kerckaert, Gary A.; LeBoeuf, Robert A.; Isfort, Robert J.; Aardema, Marilyn J.; Mutation Research - Genetic Toxicology and Environmental Mutagenesis; vol. 392; nb. 1-2; (1997); p. 61 - 70, View in Reaxys 43 of 45

Effect (Pharmacological Data)

genetic toxicity in vitro

Species or Test-System (Pharmacological Data)

Syrian hamster embryo (SHE) cells

Concentration (Pharmacological Data)

3500 - 5000 mg/l

Exposure Period (Pharmacological Data)

24 h

Method (Pharmacological Data)

micronucleus test performed; the percentage of binucleated cells ( percent BN)-500 cells analyzed and micronucleated cells ( percent MNBC)-1000 cells analyzed, determined

Further Details (Pharmacological Data)

relative cell number (number of live cells in treated/number of live cells in the solvent control*100) determined

Results

relative cell number: 96, 100 and 89 percent, percent BN: 64, 66 and 67 percent, percent MNBC: 1.3, 1.0 and 0.9 percent at the dose 3500, 4000 and 5000 μg/ml, resp.

Effect (Pharmacological Data)

toxicity, chronic

Species or Test-System (Pharmacological Data)

Long-Evans rat

Sex

male and female

Route of Application

inhalation

Concentration (Pharmacological Data)

100 - 200 ppm

Kind of Dosing (Pharmacological Data)

two doses, 100 and 200 ppm

Exposure Period (Pharmacological Data)

Method (Pharmacological Data)

mortality, body and organ (brain, liver, kidney, lungs, heart) weight recording; complete necropsies and histopathlogy examination; serum chemistry examination and hematological study

Griffin, Travis B.; Coulston, Frederick; Stein, Arthur A.; Ecotoxicology and Environmental Safety; vol. 34; nb. 2; (1996); p. 109 - 117, View in Reaxys 45 of 45

Comment (Pharmacological Data)

molar solubilities in blood

Kamlet; Abraham; Doherty; Taft; Journal of Pharmaceutical Sciences; vol. 75; nb. 4; (1986); p. 350 - 355, View in Reaxys Ecotoxicology (3) 1 of 3

Effect (Ecotoxicology)

phytotoxicity

Endpoint of Effect (Ecotoxicology)

algal growth

Species or Test-System (Ecotoxicology)

Ankistrodesmus braunii CCAP 202-7a

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Concentration (Ecotoxicology)

1.0E-3 mol/dm3

Kind of Dosing (Ecotoxi- title comp. in BBM cology) Method (Ecotoxicology)

algae were grown in title comp.-containing BBM at 23 deg C and 16 h light-8 h dark photoperiod; growth of algae was monitored daily; colorimetry at 550 nm

Further Details (Ecotoxi- Bold's Basal Medium (BBM) cology) Comment (Ecotoxicology)

No effect

Andreozzi; Lo Casale; Marotta; Pinto; Pollio; Water Research; vol. 34; nb. 18; (2000); p. 4419 - 4429, View in Reaxys 2 of 3

Effect (Ecotoxicology)

phytotoxicity

Endpoint of Effect (Ecotoxicology)

algal growth

Species or Test-System (Ecotoxicology)

Selenastrum capricornutum UTEX 1648

Concentration (Ecotoxicology)

1.0E-3 mol/dm3

Kind of Dosing (Ecotoxi- title comp. in BBM cology) Method (Ecotoxicology)

algae were grown in title comp.-containing BBM at 23 deg C and 16 h light-8 h dark photoperiod; growth of algae was monitored daily; colorimetry at 550 nm

Further Details (Ecotoxi- Bold's Basal Medium (BBM) cology) Comment (Ecotoxicology)

No effect

Andreozzi; Lo Casale; Marotta; Pinto; Pollio; Water Research; vol. 34; nb. 18; (2000); p. 4419 - 4429, View in Reaxys 3 of 3

Effect (Ecotoxicology)

toxicity to bacteria

Species or Test-System (Ecotoxicology)

Salmonella typhimurium TA100

Exposure Period (Ecotoxicology)

20 min

Method (Ecotoxicology)

toxicity test; two-fold dilution series averaging the highest conc. with no apparent toxic effect and lowest conc. for complete cell death; in 0.7 ml of incubation mixture; toxicity estimated as MLC (minimum observable lethal conc.)

Further Details (Ecotoxi- incubation mixture: sodium phosphate buffer (0.5 ml, 100 mM, pH 7.4), 0.1 ml of overnight cology) bacterial culture, title comp. (in DMSO); with or without 14 mM GSH (glutathione) Type (Ecotoxicology)

MLC

Value of Type (Ecotoxicology)

> 14 mmol/l

Results

no effect of GSH

Schneider, Manfred; Quistad, Gary B.; Casida, John E.; Mutation Research - Genetic Toxicology and Environmental Mutagenesis; vol. 439; nb. 2; (1999); p. 233 - 238, View in Reaxys Transport and Distribution (3) 1 of 3

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

air - Leonardite humic acid

Results

Leonardite humic acid/air partition coefficient, KHA,air = 1.56E3 - 4.27E3 l/kgHA; relative humidity affected experimental partition coefficient by up to a factor of 3

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Method, Remarks (Transport and Distribution)

dynamic flow-through technique; IGC-FID; title comp. injected onto the column packed with humic acid (<2 μm thick) coated glass beads; equilibrated at least 48 h; <0.01 percent-98 percent relative humidity; 15 deg C; relative humidity effect on partition equilibrium

Niederer, Christian; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 40; nb. 17; (2006); p. 5368 - 5373, View in Reaxys 2 of 3

Type (Transport and Distribution)

sorption

Media (Transport and Distribution)

air - Leonardite humic acid

Results

experimental sorption enthalpy, ΔabsHi = -37.7 kJ/mol

Method, Remarks (Transport and Distribution)

dynamic flow-through technique; IGC-FID; title comp. injected onto the column packed with humic acid (<2 μm thick) coated glass beads; equilibrated for 80 d; 98 percent relative humidity; 5 to 75 deg C

Niederer, Christian; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 40; nb. 17; (2006); p. 5368 - 5373, View in Reaxys 3 of 3

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

air - Leonardite humic acid

Results

Leonardite humic acid/air partition coefficient, KHA,air = 4.14E2 - 2.90E3 l/kgHA; no glass transitions below 75 deg C that had an effect on the sorption properties of humic acid as indicated by linear van't Hoff plot

Method, Remarks (Transport and Distribution)

Niederer, Christian; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 40; nb. 17; (2006); p. 5368 - 5373, View in Reaxys Abiotic Degradation, Hydrolysis (1) 1 of 1

Type (Abiotic Degradation, Hydrolysis)

reduction

Concentration (Abiotic Degradation, Hydrolysis)

706.9 μmol/l

Degradation Rate (Abio- 100 percent tic Degradation, Hydrolysis) [%] Exposure Period (Abiotic Degradation, Hydrolysis)

Ca. 8 h

Temperature (Abiotic Degradation, Hydrolysis) [°C]

Rate Constant

0.08 - 0.5 per hour

pH-Value (Abiotic Degradation, Hydrolysis)

7.5

Method, Remarks (Abio- batch exp.; anaerobic; title comp. in methanol or MTBE; in serum bottles with carbonate tic Degradation, Hydrol- green rust suspension; with MOPS or carbonate buffer; mixed at 50 rpm; GC-FID; HPLC; ysis) faster title comp. degradation in MOPS buffer; pseudo-first-order kinetics; fig. Degradation Product (Abiotic Degradation, Hydrolysis)

methylamine

Chun, Chan Lan; Hozalski, Raymond M.; Arnold, William A.; Environmental Science and Technology; vol. 41; nb. 5; (2007); p. 1615 - 1621, View in Reaxys Oxygen Demand (1) 1 of 1

Type (Oxygen Demand)

COD/ThOD

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Related to

Substance

Ratio BOD5/COD

0.84

Method, Remarks (Oxygen Demand)

ThOD: theoretical oxygen demand; COD determined according to Standard Methods (1976) using MilliQ water and potassium dichromate; ThOD is the stoichiometric amount of oxygen required to oxidize a compound to end product

Baker, James R.; Milke, Mark W.; Mihelcic, James R.; Water Research; vol. 33; nb. 2; (1999); p. 327 - 334, View in Reaxys Use (6) Use Pattern

References

reaction solvent

Patent; Kowa Co., Ltd.; EP1627875; (2006); (A1) English, View in Reaxys

Polar aprotic solvent for preparation of silane esters

Patent; Xerox Corporation; US2006/122414; (2006); (A1) English, View in Reaxys; Patent; Xerox Corporation; EP1669362; (2006); (A1) English, View in Reaxys

stabilizer for 1 bromopropane

Patent; ALBEMARLE CORPORATION; WO2006/119213; (2006); (A2) English, View in Reaxys

acylation of aromatic compounds

Patent; Council of Scientific and Industrial Research; US2005/222465; (2005); (A1) English, View in Reaxys

non-aqueous solvent

Patent; Council of Scientific and Industrial Research; US2005/222465; (2005); (A1) English, View in Reaxys

Dichloromethane stabilizer

Patent; SHOWA DENKO K.K.; WO2005/102970; (2005); (A1) English, View in Reaxys

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