n-Butyric acid by Asch

Query Query

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Date

628 substances in Reaxys

2017-08-01 04h:34m:41s (EST)

1. Query OH

Search as: As drawn, No mixtures 2. Query

(1. Query) AND itemno in (1,2,5,6,7,8,9,10,13,15)

10 substances in Reaxys

2017-08-01 04h:38m:02s (EST)

3. Query

(2. Query) AND itemno in (1)

1 substances in Reaxys

2017-08-01 04h:39m:41s (EST)

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Reaxys ID 906770 View in Reaxys

1/1 CAS Registry Number: 107-92-6 Chemical Name: butyric acid; butanoic acid; butyric Acid Linear Structure Formula: C4H7O2H Molecular Formula: C4H8O2 Molecular Weight: 88.1063 Type of Substance: acyclic InChI Key: FERIUCNNQQJTOY-UHFFFAOYSA-N Note:

HO O

Substance Label (157) Label References 9

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Mamedov; Mahmudova; Salmanova; Russian Journal of General Chemistry; vol. 84; nb. 9; (2014); p. 1662 - 1666; Zh. Obshch. Khim.; vol. 84; nb. 9; (2014); p. 1420 - 1424,5, View in Reaxys

Damio, Mariana C. F. C. B.; Pasqualoto, Kerly F. M.; Ferreira, Adilson K.; Teixeira, Sarah F.; Azevedo, Ricardo A.; Barbuto, Jos A. M.; Palace-Berl, Fanny; Franchi-Junior, Gilberto C.; Nowill, Alexre E.; Tavares, Maurcio T.; Parise-Filho, Roberto; Archiv der Pharmazie; vol. 347; nb. 12; (2014); p. 885 - 895, View in Reaxys

Schwartz Radatz, Cátia; Rampon, Daniel S.; Balaguez, Renata A.; Alves, Diego; Schneider, Paulo Henrique; European Journal of Organic Chemistry; vol. 2014; nb. 31; (2014); p. 6945 - 6952, View in Reaxys

Ac2

Zhu, Jian Cai; Niu, Yun Wei; Feng, Tao; Liu, Sheng Jiang; Cheng, He Xing; Xu, Na; Yu, Hai Yan; Xiao, Zuo Bing; Natural Product Research; vol. 28; nb. 21; (2014); p. 1887 - 1893, View in Reaxys

Wood, William F.; Parker, Joshua M.; Weldon, Paul J.; Journal of Chemical Ecology; vol. 21; nb. 2; (1995); p. 213 - 220, View in Reaxys; Yusubov; Filimonov; Chi, Ki-Whan; Russian Chemical Bulletin; vol. 50; nb. 4; (2001); p. 649 - 653, View in Reaxys; Hou, Zhenshan; Theyssen, Nils; Brinkmann, Axel; Leitner, Walter; Angewandte Chemie - International Edition; vol. 44; nb. 9; (2005); p. 1346 - 1349, View in Reaxys; Samanta, Sanjay; Lim, Ting Liang; Lam, Yulin; ChemMedChem; vol. 8; nb. 6; (2013); p. 994 - 1001, View in Reaxys

Lu, Jun; Yang, Bingqin; Bai, Yinjuan; Synthetic Communications; vol. 32; nb. 24; (2002); p. 3703 - 3709, View in Reaxys; Zhang, Junliang; Qu, Huan; Yu, Xiang; Zhi, Xiaoyan; Chen, Hui; Xu, Hui; Combinatorial Chemistry and High Throughput Screening; vol. 16; nb. 5; (2013); p. 394 - 399, View in Reaxys

5/428

2017-08-01 04:43:04

12c

Delpiccolo, Carina M.L.; Testero, Sebastian A.; Leyes, Federico N.; Boggian, Dora B.; Camacho, Cristian M.; Mata, Ernesto G.; Tetrahedron; vol. 68; nb. 52; (2012); p. 10780 - 10786, View in Reaxys; He, Shuzhen; Shao, Yonghua; Fan, Lingling; Che, Zhiping; Xu, Hui; Zhi, Xiaoyan; Wang, Juanjuan; Yao, Xiaojun; Qu, Huan; Journal of Agricultural and Food Chemistry; vol. 61; nb. 3; (2013); p. 618 - 625, View in Reaxys

Sutter, Marc; Dayoub, Wissam; Metay, Estelle; Raoul, Yann; Lemaire, Marc; ChemSusChem; vol. 5; nb. 12; (2012); p. 2397 - 2409, View in Reaxys; Bian, Haiyong; Feng, Jinhong; Xu, Wenfang; Medicinal Chemistry Research; vol. 22; nb. 1; (2013); p. 175 - 185, View in Reaxys

7bs

Kongkathip, Boonsong; Akkarasamiyo, Sunisa; Hasitapan, Komkrit; Sittikul, Pichamon; Boonyalai, Nonlawat; Kongkathip, Ngampong; European Journal of Medicinal Chemistry; vol. 60; (2013); p. 271 - 284, View in Reaxys

Glaszczka, Rafal; Jazwinski, Jaroslaw; Journal of Molecular Structure; vol. 1036; (2013); p. 78 - 89, View in Reaxys

13b

Guo, Yong; Fan, Lingling; Wang, Juanjuan; Yang, Chun; Qu, Huan; Xu, Hui; Tetrahedron; vol. 69; nb. 2; (2013); p. 774 - 781, View in Reaxys

Chawla, Ruchi; Singh, Atulk.; Yadav, Laldhar S.; Synlett; vol. 24; nb. 12; (2013); p. 1558 - 1562; Art.No: ST-2013-D0409-L, View in Reaxys

2u; 2s

Shaikh, Tanveer Mahammadali; Hong, Fung-E; Tetrahedron; vol. 69; nb. 42; (2013); p. 8929 - 8935, View in Reaxys

Che, Zhiping; Yu, Xiang; Zhi, Xiaoyan; Fan, Lingling; Yao, Xiaojun; Xu, Hui; Journal of Agricultural and Food Chemistry; vol. 61; nb. 34; (2013); p. 8148 - 8155, View in Reaxys

10a

Chudasama, Vijay; Akhbar, Ahmed R.; Bahou, Karim A.; Fitzmaurice, Richard J.; Caddick, Stephen; Organic and Biomolecular Chemistry; vol. 11; nb. 42; (2013); p. 7301 - 7317, View in Reaxys

Sutter, Marc; Dayoub, Wissam; Metay, Estelle; Raoul, Yann; Lemaire, Marc; ChemCatChem; vol. 5; nb. 10; (2013); p. 2893 - 2904, View in Reaxys

Morales-Serna, Jose Antonio; Sauza, Alejandro; Padron De Jesus, Gabriela; Gavino, Ruben; Garcia De La Mora, Gustavo; Cardenas, Jorge; Tetrahedron Letters; vol. 54; nb. 52; (2013); p. 7111 - 7114, View in Reaxys

Zhang, Chong-Jing; Tan, Chelsea Y. J.; Ge, Jingyan; Na, Zhenkun; Chen, Grace Y. J.; Uttamchandani, Mahesh; Sun, Hongyan; Yao, Shao Q.; Angewandte Chemie - International Edition; vol. 52; nb. 52; (2013); p. 14060 - 14064; Angew. Chem.; vol. 125; nb. 52; (2013); p. 14310 - 14314,5, View in Reaxys

Balaraman, Ekambaram; Khaskin, Eugene; Leitus, Gregory; Milstein, David; Nature Chemistry; vol. 5; nb. 2; (2013); p. 122 - 125, View in Reaxys

educt to 14g

Chen, Qiu; Liu, Fangming; Xu, Feng; Yang, Chun; Journal of Heterocyclic Chemistry; vol. 45; nb. 1; (2008); p. 77 - 83, View in Reaxys

tab.1, entry 4, acid

Li, Yangmei; Yu, Yongping; Giulianotti, Marc; Houghten, Richard A.; Tetrahedron Letters; vol. 49; nb. 22; (2008); p. 3632 - 3633, View in Reaxys

Gaviglio, Carina; Doctorovich, Fabio; Journal of Organic Chemistry; vol. 73; nb. 14; (2008); p. 5379 5384, View in Reaxys

2i, 5d, 7d

Khurana; Sharma; Gogia; Kandpal; Organic Preparations and Procedures International; vol. 39; nb. 2; (2007); p. 185 - 189, View in Reaxys

Table 2., Entry 6., NuH

Yu, Lei; Chen, Bo; Huang, Xian; Tetrahedron Letters; vol. 48; nb. 6; (2007); p. 925 - 927, View in Reaxys

Ciabatti, Romeo; Maffioli, Sonia I.; Panzone, Gianbattista; Canavesi, Augusto; Michelucci, Elena; Tiseni, Paolo S.; Marzorati, Ettore; Checchia, Anna; Giannone, Matteo; Jabes, Daniela; Romano, Gabriella; Brunati, Cristina; Candiani, Gianpaolo; Castiglione, Franca; Journal of Medicinal Chemistry; vol. 50; nb. 13; (2007); p. 3077 - 3085, View in Reaxys

Product T2/13

Uozumi, Yasuhiro; Nakao, Ryu; Rhee, Hakjune; Journal of Organometallic Chemistry; vol. 692; nb. 1-3; (2007); p. 420 - 427, View in Reaxys

tabl.1,ent.7, acid

Gang, Li; Xinzong, Li; Eli, Wumanjiang; New Journal of Chemistry; vol. 31; nb. 3; (2007); p. 348 - 351, View in Reaxys

Tab. 2, entry 8

Kirillova, Marina V.; Da Silva, Jose A. L.; Da Silva, Joao J. R. Frausto; Palavra, Antonio F.; Pombeiro, Armando J. L.; Advanced Synthesis and Catalysis; vol. 349; nb. 10; (2007); p. 1765 - 1774, View in Reaxys

6/428

2017-08-01 04:43:04

CH3(CH2)2COO H

Shi, Ji-Liang; Qiu, Zhi-Hai; Jiang, Xi-Kui; Journal of Physical Organic Chemistry; vol. 12; nb. 10; (1999); p. 735 - 740, View in Reaxys; Chakraborty; Kumar, S. Uday; Mohan, B. Krishna; Sarma, G. Dattatreya; Kiran, M. Udaya; Jagadeesh; Tetrahedron Letters; vol. 48; nb. 39; (2007); p. 6945 - 6950, View in Reaxys

EtCH2COOH

Ullah, Ehsan; Langer, Peter; Synlett; nb. 15; (2004); p. 2782 - 2784, View in Reaxys; Zhou, Aihua; Pittman Jr., Charles U.; Synthesis; nb. 1; (2006); p. 37 - 48; Art.No: M01705SS, View in Reaxys; Jeon, Moon-Kook; Hyun, Ju La; Ha, Deok-Chan; Gong, Young-Dae; Synlett; nb. 9; (2007); p. 1431 - 1435, View in Reaxys

Smicius, Romualdas; Burbuliene, Milda Malvina; Jakubkiene, Virginija; Udrenaite, Emilija; Vainilavicius, Povilas; Journal of Heterocyclic Chemistry; vol. 44; nb. 2; (2007); p. 279 - 284, View in Reaxys

Tab.1.cl.3. run 5

Ye, Suming; Leong, Weng Kee; Journal of Organometallic Chemistry; vol. 691; nb. 6; (2006); p. 1216 1222, View in Reaxys

Katritzky, Alan R.; Singh, Sandeep K.; Jiang, Rong; Tetrahedron; vol. 62; nb. 16; (2006); p. 3794 - 3797, View in Reaxys

Mendez, Jonh Jairo; Eras, Jordi; Balcells, Merce; Canela, Ramon; Synthetic Communications; vol. 36; nb. 9; (2006); p. 1167 - 1175, View in Reaxys

T. 1., E. 16., R'COOH

Li, Wenji; Thakur, Santosh Singh; Chen, Shu-Wei; Shin, Chang-Kyo; Kawthekar, Rahul B.; Kim, GeonJoong; Tetrahedron Letters; vol. 47; nb. 20; (2006); p. 3453 - 3457, View in Reaxys

R'COOH, R'=nC3H7

Thakur, Santosh Singh; Chen, Shu-Wei; Li, Wenji; Shin, Chang-Kyo; Kim, Seong-Jin; Koo, Yoon-Mo; Kim, Geon-Joong; Journal of Organometallic Chemistry; vol. 691; nb. 9; (2006); p. 1862 - 1872, View in Reaxys

Fan, Xuesen; Li, Yanzhen; Zhang, Xinying; Qu, Guirong; Wang, Jianji; Canadian Journal of Chemistry; vol. 84; nb. 5; (2006); p. 794 - 799, View in Reaxys

tab. 1, entry 9, acid

Mukherjee, Chandrani; Zhu, Dunming; Biehl, Edward R.; Hua, Ling; European Journal of Organic Chemistry; nb. 23; (2006); p. 5238 - 5242, View in Reaxys

Conway, Stuart J.; Thuring, Jan W.; Andreu, Sylvain; Kvinlaug, Brynn T.; Roderick, H. Llewelyn; Bootman, Martin D.; Holmes, Andrew B.; Australian Journal of Chemistry; vol. 59; nb. 12; (2006); p. 887 - 893; Art.No: CH06357, View in Reaxys

Li, Yun-Fei; Wang, Gui-Feng; He, Pei-Lan; Huang, Wei-Gang; Zhu, Feng-Hua; Gao, He-Yong; Tang, Wei; Luo, Yu; Feng, Chun-Lan; Shi, Li-Ping; Ren, Yu-Dan; Lu, Wei; Zuo, Jian-Ping; Journal of Medicinal Chemistry; vol. 49; nb. 15; (2006); p. 4790 - 4794, View in Reaxys

table 3, 27

Abraham, Raymond J.; Byrne, Jonathan J.; Griffiths, Lee; Perez, Manuel; Magnetic Resonance in Chemistry; vol. 44; nb. 5; (2006); p. 491 - 509, View in Reaxys

substrate to IV, IX Alagarsamy, Veerachamy; Yadav, Mangae Ram; Giridhar, Rajani; Arzneimittel-Forschung/Drug Research; vol. 56; nb. 12; (2006); p. 834 - 841, View in Reaxys 35

Machado, Luciana L.; Souza, Joao Sammy N.; de Mattos, Marcos Carlos; Sakata, Solange K.; Cordell, Geoffrey A.; Lemos, Telma L.G.; Phytochemistry; vol. 67; nb. 15; (2006); p. 1637 - 1643, View in Reaxys

n-Pr-CO2H

Sung, Kuangsen; Chen, Fu-Lin; Huang, Pei-Chun; Synlett; nb. 16; (2006); p. 2667 - 2669, View in Reaxys

C3H7COOH

Lokot'; Pashkovskii; Lakhvich; Russian Journal of Organic Chemistry; vol. 35; nb. 5; (1999); p. 746 - 755, View in Reaxys; Srinivasulu; Pratap Reddy; Hegde, Pragathi; Chakrabart, Ranjan; Heterocyclic Communications; vol. 11; nb. 1; (2005); p. 23 - 28, View in Reaxys

Chapman, Timothy M.; Davies, Ieuan G.; Gu, Baohua; Block, Timothy M.; Scopes, David I. C.; Hay, Philip A.; Courtney, Stephen M.; McNeill, Luke A.; Schofield, Christopher J.; Davis, Benjamin G.; Journal of the American Chemical Society; vol. 127; nb. 2; (2005); p. 506 - 507, View in Reaxys

1/Tab.1.run1

Hamilakis, Stylianos; Tsolomitis, Athanase; Heterocyclic Communications; vol. 11; nb. 2; (2005); p. 149 152, View in Reaxys

6b; n-PrCOOH

Weiwer; Olivero; Dunach; Tetrahedron; vol. 61; nb. 7; (2005); p. 1709 - 1714, View in Reaxys

tab2, product2, run12

Wang, Jianmin; Yan, Liang; Li, Guixian; Wang, Xiaolai; Ding, Yong; Suo, Jishuan; Tetrahedron Letters; vol. 46; nb. 41; (2005); p. 7023 - 7027, View in Reaxys

Lin, Qi; O'Neill, Jennifer C.; Blackwell, Helen E.; Organic Letters; vol. 7; nb. 20; (2005); p. 4455 - 4458, View in Reaxys

Bali, Alka; Bansal, Yogita; Sugumaran; Saggu, Jatinder Singh; Balakumar; Kaur, Gurpreet; Bansal, Gulshan; Sharma, Ajay; Singh, Manjeet; Bioorganic and Medicinal Chemistry Letters; vol. 15; nb. 17; (2005); p. 3962 - 3965, View in Reaxys

Bandgar; Bettigeri; Synthetic Communications; vol. 34; nb. 16; (2004); p. 2917 - 2924, View in Reaxys; Geske, Grant D.; Wezeman, Rachel J.; Siegel, Adam P.; Blackwell, Helen E.; Journal of the American Chemical Society; vol. 127; nb. 37; (2005); p. 12762 - 12763, View in Reaxys

7/428

2017-08-01 04:43:04

C3H7CO2H

Schobert, Rainer; Jagusch, Carsten; Synthesis; nb. 14; (2005); p. 2421 - 2425; Art.No: T03605SS, View in Reaxys

2c, R=C3H7

Ivanov, Iliyan; Nikolova, Stoyanka; Statkova-Abeghe, Stela; Heterocycles; vol. 65; nb. 10; (2005); p. 2483 - 2492, View in Reaxys

n-PrCOOH

Zhang, Yonghui; Xu, Chengfu; Li, Jinfeng; Yuan, Chengye; Tetrahedron Asymmetry; vol. 14; nb. 1; (2003); p. 63 - 70, View in Reaxys; Sanchez-Viesca; Gomez; Berros, Martha; Heterocyclic Communications; vol. 9; nb. 4; (2003); p. 367 - 372, View in Reaxys; Xu, Chengfu; Zhang, Yonghui; Yuan, Chengye; Synlett; nb. 3; (2004); p. 485 - 488, View in Reaxys; Wang, Ke; Zhang, Yonghui; Yuan, Chengye; Organic and Biomolecular Chemistry; vol. 1; nb. 20; (2003); p. 3564 - 3569, View in Reaxys; Kolosov; Orlov; Chemistry of Heterocyclic Compounds; vol. 41; nb. 2; (2005); p. 260 - 261, View in Reaxys

III

Fushinobu, Shinya; Jun, So-Young; Hidaka, Masafumi; Nojiri, Hideaki; Yamane, Hisakazu; Shoun, Hirofumi; Omori, Toshio; Wakagi, Takayoshi; Bioscience, Biotechnology and Biochemistry; vol. 69; nb. 3; (2005); p. 491 - 498, View in Reaxys

PrCOOH

Goswami, Garima; Kothari, Seema; Banerji, Kalyan K.; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 38; nb. 11; (1999); p. 1270 - 1273, View in Reaxys; Kim, Yong; You, Ng-Jae; Ahn, Byung-Zun; Archiv der Pharmazie; vol. 334; nb. 10; (2001); p. 318 - 322, View in Reaxys; Salechi; Khodaei; Ghareghani; Motlagh; Russian Journal of Organic Chemistry; vol. 39; nb. 6; (2003); p. 794 - 796, View in Reaxys; Kozlov; Gusak; Tereshko; Dikusar; Russian Journal of Organic Chemistry; vol. 40; nb. 5; (2004); p. 705 - 710, View in Reaxys

R2-CO2H, R2=nC3H7

Banfi, Luca; Basso, Andrea; Guanti, Giuseppe; Riva, Renata; Tetrahedron Letters; vol. 45; nb. 35; (2004); p. 6637 - 6640, View in Reaxys

n-PrCO2H

Xu, Chengfu; Yuan, Chengye; Synthesis; nb. 15; (2004); p. 2449 - 2458, View in Reaxys

educt to 14

Xu, Zhi-Dong; Wang, Min; Xiao, So-Long; Zhang, Yan-Juan; Yang, Ming; Helvetica Chimica Acta; vol. 87; nb. 11; (2004); p. 2834 - 2841, View in Reaxys

educt to I.4-5, II.5

Gasowska; Dabrowski; Drzewinski; Kenig; Tykarska; Przedmojski; Molecular Crystals and Liquid Crystals; vol. 411; (2004); p. 231/[1273]-241/[1283], View in Reaxys

acid for II

Galanin; Kudrik; Shaposhnikov; Russian Journal of General Chemistry; vol. 74; nb. 2; (2004); p. 282 - 285, View in Reaxys

Tble 1, acid, row =9

Basso, Andrea; Banfi, Luca; Guanti, Giuseppe; Riva, Renata; Riu, Antonella; Tetrahedron Letters; vol. 45; nb. 32; (2004); p. 6109 - 6111, View in Reaxys

educt to (R,R)-29

Behr, Sandra; Hegemann, Klaus; Schimanski, Holger; Froehlich, Roland; Haufe, Guenter; European Journal of Organic Chemistry; nb. 18; (2004); p. 3884 - 3892, View in Reaxys

n-C3H7COOH

Iki, Nobuhiko; Suzuki, Takehiro; Koyama, Katsuyoshi; Kabuto, Chizuko; Miyano, Sotaro; Organic Letters; vol. 4; nb. 4; (2002); p. 509 - 512, View in Reaxys; Cao, Linghua; Zhang, Lin; Cui, Pengyuan; Chemistry of Heterocyclic Compounds; vol. 40; nb. 5; (2004); p. 635 - 640, View in Reaxys

educt to 20

Kraft, Philip; Eichenberger, Walter; European Journal of Organic Chemistry; nb. 2; (2004); p. 354 - 365, View in Reaxys

Tab. 1

Sloboda-Rozner, Dorit; Witte, Peter; Alsters, Paul L.; Neumann, Ronny; Advanced Synthesis and Catalysis; vol. 346; nb. 2-3; (2004); p. 339 - 345, View in Reaxys

acid to 1

Chakraborty; Krishna Mohan; Uday Kumar; Prabhakar; Jagadeesh; Tetrahedron Letters; vol. 45; nb. 29; (2004); p. 5623 - 5627, View in Reaxys

HBu

Lin, Chiu-Yue; Chen, Chin-Chao; Water Research; vol. 33; nb. 2; (1999); p. 409 - 416, View in Reaxys; Ahn, Young-Ho; Min, Kyung-Sok; Speece, Richard E; Water Research; vol. 35; nb. 18; (2001); p. 4267 4276, View in Reaxys; McRae; Patterson; Origlia-Luster; Sorenson; Woolley; Journal of Chemical Thermodynamics; vol. 35; nb. 2; (2003); p. 301 - 329, View in Reaxys; Yu, Han Qing; Fang, Herbert H.P; Water Research; vol. 37; nb. 1; (2003); p. 55 - 66, View in Reaxys

Nery, Marcelo S.; Ribeiro, Renata P.; Lopes, Claudio C.; Lopes, Rosangela S. C.; Synthesis; nb. 2; (2003); p. 272 - 276, View in Reaxys

Product (entry 13) Uozumi, Yasuhiro; Nakao, Ryu; Angewandte Chemie - International Edition; vol. 42; nb. 2; (2003); p. 194 197, View in Reaxys acid f

Bandgar; Pandit; Tetrahedron Letters; vol. 44; nb. 11; (2003); p. 2331 - 2333, View in Reaxys

Scardovi, Noemi; Garner, Philip P.; Protasiewicz, John D.; Organic Letters; vol. 5; nb. 10; (2003); p. 1633 - 1635, View in Reaxys

11m

Ravn, Jacob; Ankersen, Michael; Begtrup, Mikael; Lau, Jesper F.; Tetrahedron Letters; vol. 44; nb. 36; (2003); p. 6931 - 6935, View in Reaxys

8/428

2017-08-01 04:43:04

acid for 14g

Goujon, Jean-Yves; Gueyrard, David; Compain, Philippe; Martin, Olivier R.; Asano, Naoki; Tetrahedron Asymmetry; vol. 14; nb. 14; (2003); p. 1969 - 1972, View in Reaxys

tab2, acid, entry3

Kawamura, Masato; Cui, Dong-Mei; Hayashi, Teruyuki; Shimada, Shigeru; Tetrahedron Letters; vol. 44; nb. 42; (2003); p. 7715 - 7717, View in Reaxys

D, R-COOH, R=C3H7

Goswami, Papori; Hazarika, Saroj; Borah, Parinita; Chowdhury, Pritish; Indian Journal of Chemistry Section B Organic and Medicinal Chemistry; vol. 42; nb. 3; (2003); p. 678 - 682, View in Reaxys

Voronkov; Belousova; Trukhina; Vlasova; Russian Journal of Organic Chemistry; vol. 39; nb. 12; (2003); p. 1702 - 1705, View in Reaxys

capping comp. 3

Holder, Jerry Ryan; Marques, Fernanda F.; Xiang, Zhimin; Bauzo, Rayna M.; Haskell-Luevano, Carrie; European Journal of Pharmacology; vol. 462; nb. 1-3; (2003); p. 41 - 52, View in Reaxys

CH3CH2CH2CO2 Wang; Manku; Hall; Organic letters; vol. 2; nb. 11; (2000); p. 1581 - 1583, View in Reaxys; Andrade, Carlos H Kleber Z.; Rocha, Rafael O.; Vercillo, Otilie E.; Silva, Wender A.; Matos, Ricardo Alexandre F.; Synlett; nb. 15; (2003); p. 2351 - 2352, View in Reaxys Me(CH2)2CO2H

Acharya, Achyuta N; Ostresh, John M; Houghten, Richard A; Tetrahedron Letters; vol. 43; nb. 7; (2002); p. 1157 - 1160, View in Reaxys

Substr., Tab.2, run 12

Cho, Chan Sik; Kim, Dong Tak; Zhang, Jiao Qiang; Ho, Son-Lam; Kim, Tae-Jeong; Shim, Sang Chul; Journal of Heterocyclic Chemistry; vol. 39; nb. 2; (2002); p. 421 - 423, View in Reaxys

acid for 4e

Csaky, Aurelio G.; Mula; Mba, Myriam; Plumet, Joaquin; Tetrahedron Asymmetry; vol. 13; nb. 7; (2002); p. 753 - 757, View in Reaxys

Clarke, Kevin O.; Ludeman, Susan M.; Springer, James B.; Michael Colvin; Lea, Michael A.; Harrison, Lawrence E.; Journal of Pharmaceutical Sciences; vol. 91; nb. 4; (2002); p. 1054 - 1064, View in Reaxys

Substrate, Tab.2, run 4

Luo, Guanglin; Xu, Li; Poindexter, Graham S.; Tetrahedron Letters; vol. 43; nb. 49; (2002); p. 8909 - 8912, View in Reaxys

starting to 3b

De Almeida, Paulo Afonso; Da Silva, Tania Maria Sarmento; Echevarria, Aurea; Heterocyclic Communications; vol. 8; nb. 6; (2002); p. 593 - 600, View in Reaxys

C-4

Pedersen, Ninfa R; Wimmer, Reinhard; Emmersen, Jeppe; Degn, Peter; Pedersen, Lars H; Carbohydrate research; vol. 337; nb. 13; (2002); p. 1179 - 1184, View in Reaxys

CH3CH2CH2CO OH

Jagtap, Prakash G.; Baloglu, Erkan; Barron, Donna M.; Bane, Susan; Kingston, David G. I.; Journal of Natural Products; vol. 65; nb. 8; (2002); p. 1136 - 1142, View in Reaxys

Patent; Beacon Laboratories, Inc.; EP1216986; (2002); (A2) English, View in Reaxys

educt of 1,2,5,6

Ikeda, Tsukasa; Kajiyama, Koshiro; Kita, Toshikazu; Takiguchi, Noboru; Kuroda, Akio; Kato, Junichi; Ohtake, Hisao; Chemistry Letters; nb. 4; (2001); p. 314 - 315, View in Reaxys

Szajnman, Sergio H.; Bailey, Brian N.; Docampo, Roberto; Rodriguez, Juan B.; Bioorganic and Medicinal Chemistry Letters; vol. 11; nb. 6; (2001); p. 789 - 792, View in Reaxys

nBa

Hull; Cribb; Journal of Chemical Ecology; vol. 27; nb. 5; (2001); p. 871 - 887, View in Reaxys

Merck 1629

Dyer, Kimberly; Rosenberg, Helene; Life Sciences; vol. 69; nb. 2; (2001); p. 201 - 212, View in Reaxys

nC3H7-COOH

Bjorsvik; Fontana; Liguori; Minisci; Chemical Communications; nb. 6; (2001); p. 523 - 524, View in Reaxys

Zara, Cynthia Lynn; Jin, Thomas; Giguere, Raymond J.; Synthetic Communications; vol. 30; nb. 12; (2000); p. 2099 - 2104, View in Reaxys

MeCH2CH2COOH

Nefzi, Adel; Ong, Nhi A.; Houghten, Richard A.; Tetrahedron Letters; vol. 41; nb. 29; (2000); p. 5441 5446, View in Reaxys

C65

Boger, Dale L.; Goldberg, Joel; Satoh, Shigeki; Ambroise, Yves; Cohen, Steven B.; Vogt, Peter K.; Helvetica Chimica Acta; vol. 83; nb. 8; (2000); p. 1825 - 1845, View in Reaxys

Stromgaard; Brier; Andersen; Mellor; Saghyan; Tikhonov; Usherwood; Krogsgaard-Larsen; Jaroszewski; Journal of Medicinal Chemistry; vol. 43; nb. 23; (2000); p. 4526 - 4533, View in Reaxys

Goswami; Chowdhury; New Journal of Chemistry; vol. 24; nb. 12; (2000); p. 955 - 957, View in Reaxys

nPrCO2H

Banfi, Luca; Guanti, Giuseppe; Riva, Renata; Chemical Communications; nb. 11; (2000); p. 985 - 986, View in Reaxys

RC(O)X,t.1, entry 4

Dragovich, Peter S.; Zhou, Ru; Skalitzky, Donald J.; Fuhrman, Shella A.; Patick, Amy K.; Ford, Clifford E.; Meador III, James W.; Worland, Stephen T.; Bioorganic and Medicinal Chemistry; vol. 7; nb. 4; (1999); p. 589 - 598, View in Reaxys

9/428

2017-08-01 04:43:04

1, R=n-Pr

Asadullah, Mohammad; Kitamura, Tsugio; Fujiwara, Yuzo; Chemistry Letters; nb. 6; (1999); p. 449 - 450, View in Reaxys

acid for 28

Boyd, Steven A.; Mantei, Robert A.; Tasker, Andrew S.; Liu, Gang; Sorensen, Bryan K.; Henry Jr., Kenneth J.; Von Geldern, Thomas W.; Winn, Martin; Wu-Wong, Jinshyun R.; Chiou, William J.; Dixon, Douglas B.; Hutchins, Charles W.; Marsh, Kennan C.; Nguyen, Bach; Opgenorth, Terry J.; Bioorganic and Medicinal Chemistry; vol. 7; nb. 6; (1999); p. 991 - 1002, View in Reaxys

Table 2, entry 5

Kabalka; Li; Tejedor; Malladi; Gao; Trotman; Synthetic Communications; vol. 29; nb. 16; (1999); p. 2783 2787, View in Reaxys

n-But

Reischwitz, Astrid; Stoppok, Eberhard; Buchholz, Klaus; Biodegradation; vol. 8; nb. 5; (1997); p. 313 319, View in Reaxys

FFA C4:0

Petschow, Bryon W.; Batema, Rosanne P.; Ford, Lorna L.; Antimicrobial Agents and Chemotherapy; vol. 40; nb. 2; (1996); p. 302 - 306, View in Reaxys

n-C4-VFA

Gonzalez-Vila, F. J.; Bautista, J. M.; Rio, J. C. Del; Martin, F.; Chemosphere; vol. 31; nb. 3; (1995); p. 2817 - 2826, View in Reaxys

n-HBu

Zhang, Tian Cheng; Noike, Tatsuya; Water Research; vol. 28; nb. 1; (1994); p. 27 - 36, View in Reaxys

Patent-Specific Data (23) Prophetic ComLocation in Patent References pound Patent; Zhejiang Himpton New Material Co., Ltd.; Tang, Wei; Gao, Erjin; Ju, Yingjun; Chen, Jianjun; Liao, Yonglin; Chen, Senfang; (8 pag.); CN106279249; (2017); (A) Chinese, View in Reaxys Patent; Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences; Du, Yuguo; Qiao, Junfei; (7 pag.); CN106518805; (2017); (A) Chinese, View in Reaxys Patent; Changshu Institute of Technology; Ceng, Xiaojun; Zhao, Dengyu; Zhang, Yuming; Li, Licheng; Xu, Jiarui; Chen, Huiqin; (8 pag.); CN105732686; (2016); (A) Chinese, View in Reaxys Patent; Tianjin Institute of pharmaceutical research; Liu, Ying; Liu, DengKe; Zhang, Dashuai; Niu, Duan; Wu, jiang; Zou, meixiang; (7 pag.); CN103265607; (2016); (B) Chinese, View in Reaxys Patent; Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences; LIU, YI; LIU, JUN; DU, YUGUO; (5 pag.); CN105315226; (2016); (A) Chinese, View in Reaxys

prophetic product

Page/Page column

Patent; Vaillancourt, Valerie A.; Chubb, Nathan Anthony Logan; Curtis, Michael; Howson, William; Kyne, Graham M.; Menon, Sanjay; Sheehan, Susan M. K.; Skalitzky, Donald J.; Wendt, John A.; US2012/35122; (2012); (A1) English, View in Reaxys; Patent; INSTITUTE OF MATERIA MEDICA, CHINESE ACADEMY OF MEDICAL SCIENCES; Shi, Jiangong; Zhang, Jianjun; Yue, Zhenggang; Li, Min; Zhu, Chenggen; Zhang, Ying; Zi, Jiachen; Wang, Yafang; Fan, Xiaona; Xu, Ruiming; Lin, Sheng; Li, Yan; Yang, Yongchun; Sheng, Li; US2013/45942; (2013); (A1) English, View in Reaxys; Patent; KYOTO UNIVERSITY; Kakeya, Hideaki; Hattori, Akira; Takasu, Yasuaki; Fujii, Nobutaka; Oishi, Shinya; Kojima, Soichi; Hara, Mitsuko; US2013/45977; (2013); (A1) English, View in Reaxys; Patent; AGIOS PHARMACEUTICALS, INC; Lemieux, Rene M.; Popovici-Muller, Janeta; Salituro, Francesco G.; Saunders, Jeffrey O.; Travins, Jeremy; Chen, Yongsheng; US2014/142081; (2014); (A1) English, View in Reaxys; Patent; INSTITUTE OF MATERIA MEDICA, CHINESE ACADEMY OF MEDICAL SCIENCES; HAN, Weijuan; ZHANG, Haijing; WANG, Xiaojian; JIN, Jing; LI, Gang; ZHANG, Yi; XIAO, Qiong; ZHOU, Wanqi; CHEN, Xiaoguang; YIN, Dali; EP2786982; (2014); (A1) English, View in Reaxys; Patent; INSTITUTE OF MATERIA MEDICA, CHINESE ACADEMY OF MEDICAL SCIENCES; Han, Weijuan; Zhang, Haijing; Wang, Xiaojian; Jin, Jing; Li, Gang; Zhang, Yi; Xiao, Qiong; Zhou, Wanqi; Chen, Xiaoguang; Yin, Dali; US2014/323501; (2014); (A1) English, View in Reaxys; Patent; Hayashi, Yuya; Mizutare, Yoko; US2015/93345; (2015); (A1) English, View in Reaxys

Page/Page column

Patent; IMAX Discovery GmbH; WINNING, Marcel; LOHMER, Stefan; PEVARELLO, Paolo; EP2832233; (2015); (A1) English, View in Reaxys; Patent; IMAX Discovery GmbH; WINNING, Marcel; LOHMER, Stefan; PEVARELLO, Paolo; EP2832234; (2015); (A1) English, View in Reaxys

Page/Page column

Patent; CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE; FONDS DE DEVELOPPEMENT DES FILIERES DES OLEAGINEUX ET PROTEAGINEUX FIDOP;

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Lemaire, Marc; Dayoub, Wissam; Sutter, Marc; Raoul, Yann; US2014/18579; (2014); (A1) English, View in Reaxys prophetic product

Claim 3

Patent; LANXESS Deutschland GmbH; Kahlert, Steffen; Kaulen, Johannes; Vogl, Erasmus; US8569540; (2013); (B2) English, View in Reaxys Patent; Trauth, Daniel M.; Green, George D.; Swedo, Raymond J.; US2011/92750; (2011); (A1) English, View in Reaxys Patent; The University of Tokyo; Otsuka Chemical Co., Ltd.; EP2221293; (2010); (A1) English, View in Reaxys Patent; Amin, Neelam S.; Boston, Matthew G.; Bott, Richard R.; Cervin, Marguerite A.; Concar, Edward M.; Gustwiller, Marc E.; Jones, Brain E.; Liebeton, Klaus; Miracle, Gregory S.; Oh, Hiroshi; Poulose, Ayrookaran J.; Ramer, Sandra W.; Scheibel, Jeffrey J.; Weyler, Walter; Whited, Gregory M.; US2008/145353; (2008); (A1) English, View in Reaxys Patent; SUMITOMO CHEMICAL COMPANY, LIMITED; WO2008/126665; (2008); (A2) English, View in Reaxys

prophetic catalyst

Page/page column 19

Patent; CELGENE CORPORATION; WO2007/136640; (2007); (A2) English, View in Reaxys Patent; Norel, S.A.; EP1647542; (2006); (A1) English, View in Reaxys Patent; Air Products and Chemicals, Inc.; EP1659108; (2006); (A1) English, View in Reaxys Patent; Xerox Corporation; US2005/90690; (2005); (A1) English, View in Reaxys

prophetic product

Patent; Tosoh Corporation; US6342620; (2002); (B1) English, View in Reaxys; Patent; TOKUYAMA CORPORATION; EP1178043; (2002); (A1) English, View in Reaxys; Patent; BASF AKTIENGESELLSCHAFT; EP1186589; (2002); (A1) German, View in Reaxys; Patent; Teijin Limited; US3991099; (1976); (A1) English, View in Reaxys; Patent; Mitsui Toatsu Chemicals, Inc.; US5359117; (1994); (A1) English, View in Reaxys; Patent; Schering Aktiengesellschaft; US5501863; (1996); (A1) English, View in Reaxys; Patent; Brophy, John H.; Pesa, Frederick A.; Tonkovich, Anna Lee; McDaniel, Jeffrey S.; Jarosch, Kai Tod Paul; US2004/220434; (2004); (A1) English, View in Reaxys; Patent; Wang, Bing; Miller, Guy; Flaim, Stephen F.; Del Balzo, Ughetta; Zhang, Wei; Janagani, Satyanarayana; Song, Jiangao; US2003/13656; (2003); (A1) English, View in Reaxys; Patent; Aventis Pharmaceuticals Inc.; EP1178041; (2002); (A1) English, View in Reaxys; Patent; Ciba Specialty Chemicals Corporation; US6140326; (2000); (A1) English, View in Reaxys Patent; Mionix Corp.; US2004/171687; (2004); (A1) English, View in Reaxys Patent; Yaegashi, Keisuke; Furukawa, Yoshiro; US2004/24254; (2004); (A1) English, View in Reaxys

prophetic product

Patent; Sumitomo Chemical Company, Limited; EP1188735; (2002); (A1) English, View in Reaxys Patent; Takeda Chemical Industries, Ltd.; EP1199304; (2002); (A1) English, View in Reaxys

prophetic product

Claim

Patent; NanoSystems L.L.C.; US5662883; (1997); (A1) English, View in Reaxys

Druglikeness (1) 1 of 1

LogP

0.742

H Bond Donors

H Bond Acceptors

Rotatable Bonds

TPSA

37.3

Lipinski Number

Veber Number

Related Structure (2) Related Structure References The author has doubts about the constitution/

Shaw, Stephanie L.; Mitloehner, Frank M.; Jackson, Wendi; Depeters, Edward J.; Fadel, James G.; Robinson, Peter H.; Holzinger, Rupert; Goldstein, Allen H.; Environmental Science and Technology; vol. 41; nb. 4; (2007); p. 1310 - 1316, View in Reaxys

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configuration of the title compound Buttersaeure ist bei Raumtemperatur bimolekular.

Freri; Gazzetta Chimica Italiana; vol. 78; (1948); Atti della Accademia Nazionale dei Lincei, Classe di Scienze Fisiche, Matematiche e Naturali, Rendiconti; vol. <8>5; (1948); p. 161, View in Reaxys

Catalyst Investigation (1) 1 of 1

Investigated characteris- Catalytic activity tic(s) Type of reaction (Catalyst Investigation)

Biginelli reaction

Noreen, Sadia; Perveen, Saima; Khan, Muhammad Naeem; Nazeer, Areesha; Khan, Misbahul Ain; Munawar, Munawar Ali; Babar, Rabia; Suhail, Farah; Azad, Muhammad; Bernardino, Alice M.R.; Dos Santos, Mauricio S.; Asian Journal of Chemistry; vol. 25; nb. 9; (2013); p. 4770 - 4772, View in Reaxys Derivative (173) Comment (Derivative)

References

By formation of compound with BF3-methanol

Richardson, Susan D.; Thruston Jr., Alfred D.; Caughran, Tashia V.; Chen, Paul H.; Collette, Timothy W.; Floyd, Terrance L.; Schenck, Kathleen M.; Lykins Jr., Benjamin W.; Sun, Guang-Ri; Majetich, George; Environmental Science and Technology; vol. 33; nb. 19; (1999); p. 3368 - 3377, View in Reaxys

K-Salz: ν(2max)

Dash; Nagak; Thermochimica Acta; vol. 34; (1979); p. 387, View in Reaxys

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Addukt mit Et2O in Essigsaeure, Benzol: K (kryoskopisch)

Kulikova et al.; Russian Journal of Physical Chemistry; vol. 53; (1979); p. 1687; ; p. 2942, View in Reaxys

Addukt mit Ph2O in Essigsaeure, Benzol: K (kryoskopisch)

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Addukt mit Pr2O in Essigsaeure, Benzol: K (kryoskopisch)

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<Na>+-Salz, Adsorptionsenergie an der Oel-Wasser-Grenzflaeche

Chattoraj; Journal of the Indian Chemical Society; vol. 56; (1979); p. 1065,1067, View in Reaxys

Nickelbutyrat (IV): Kharitonova et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 49; (1979); p. 2716,2407,2408,2409, aus Nickelhydrox- View in Reaxys id und Buttersaeure; Piperidinkomplex(IV') Stabilitaetskonstante K-Salz: RamanSpektrum

Okabayashi; Kitagawa; Journal of Physical Chemistry; vol. 82; (1978); p. 1830,1833, View in Reaxys

Hg-Salz: F: 210-213grad (Zers.)

Ol'dekop et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 48; (1978); p. 426,381, View in Reaxys

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Mn-Salz: Aus dem Na-Salz, Mn2+; Pyrolyse

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K-Salz: F: Pochtakova et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 48; (1978); p. 1212,1108, View in Reaxys 404grad; Studium des Systems Kaliumbutyrat in der Schmelze Na-Salz: F: Pochtakova et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 48; (1978); p. 1212,1108, View in Reaxys 330grad; Studium des Systems Natriumbutyrat in der Schmelze Mg-Salz: F: Pochtakova et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 48; (1978); p. 1212,1108, View in Reaxys 302grad; Studium des Systems Magnesiumbutyrat in der Schmelze Komplex mit <Mg>2+; Stabil. Konst.

Fedorov; Khokhlova; Russian Journal of Inorganic Chemistry (Translation of Zhurnal Neorganicheskoi Khimii); vol. 22; (1977); p. 662, View in Reaxys

Na-Salz: Leitfaehigkeit in Sucrose-Lsg.

Vishnu; Singh; Carbohydrate Research; vol. 54; (1977); p. 149,151, View in Reaxys

Sr2+-Komplex: Bil- Fedorov; Khokhlova; Sov. J. Coord. Chem. (Engl. Transl.); vol. 3; (1977); p. 970,751,753, View in Reaxys dungskonst. (Tab. 2) Na-Salz: DiffuRigand et al.; Chemistry and Physics of Lipids; vol. 18; (1977); p. 23,29, 31, 33, 34, View in Reaxys sionskoeff. in Lecithin-Wasser-Phasen Na-Salz: isentrop. Hoiland; Vikingsstad; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Conχ densed Phases; vol. 72; (1976); p. 1441,1443, 1444, View in Reaxys Na-Salz: Therm. Verh.

Roth et al.; Journal of Thermal Analysis; vol. 10; (1976); p. 223,226, View in Reaxys

Na-Salz, el. Leitf.=f(ν,T)

Duruz; Ubbelohde; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 347; (1976); p. 301, View in Reaxys

Ba-salz: phasetransition (T; ΔH)

Ferloni et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 31; (1976); p. 679, View in Reaxys

Ca-salz: phasetransition (T; ΔH)

Ferloni et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 31; (1976); p. 679, View in Reaxys

Sr-salz: phasetransition (T; ΔH)

Ferloni et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 31; (1976); p. 679, View in Reaxys

CH3-CH2-CH2COOH-CsF-Addukt IR; 1H-NMR

Emsley; Hoyte; Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999); (1976); p. 2219, View in Reaxys

Ca-Butyrat: IRSp. (KBr, 1800-1300 cm-1)

Andor et al.; Acta Physica et Chemica; vol. 22; (1976); p. 117,122, View in Reaxys

K-Salz: Viskositaet verd. waessr. Lsgn., Molvolumen bei unendl. Verduennung (Tab.I)

Palma; Morel; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 73; (1976); p. 645,648, View in Reaxys

Na-Salz, Χ

Duruz; Ubbelohde; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 342; (1975); p. 39,43, View in Reaxys

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K+-Salz: RamanSp.

Okabayashi et al.; Bulletin of the Chemical Society of Japan; vol. 48; (1975); p. 2264, View in Reaxys

Na-Salz; Molale Kompressibilitaet (s.Tab.1)

Kaulgud; Rao; Indian Journal of Chemistry; vol. 13; (1975); p. 616, View in Reaxys

Li-Salz: Rk. m. Phenyllithium: Produktverteilung

Levine et al.; Journal of Organic Chemistry; vol. 40; (1975); p. 1770, View in Reaxys

Li-Salz: Rk. m. Grignard-Verb.: Produktverteilung

Levine et al.; Journal of Organic Chemistry; vol. 40; (1975); p. 1770, View in Reaxys

Na-salz: Best. Sakurai et al.; Bulletin of the Chemical Society of Japan; vol. 48; (1975); p. 3491,3492, View in Reaxys von Molalvolumen, Partialvolumen und Dichte in aq.Lsg. Na-Salz: Loesungsenthalpie ΔH0(s); Waermekapazitaet ΔC(p)0 in H2O

Chawla; Ahluwalia; Journal of Solution Chemistry; vol. 4; (1975); p. 383,385, View in Reaxys

K-Salz: Verteilungskoeff. H2O/n-Butanol (aus Extraktion); DissoziationsKonst. in n-BuOH (konduktometrisch und potentiometrisch)

Kuznetsova et al.; Russian Journal of Physical Chemistry; vol. 49; (1975); p. 261; ; p. 452, View in Reaxys

Na-Salz: Verteilungskoeff. H2O/n-Butanol (aus Extraktion); DissoziationsKonst. in n-BuOH (konduktometrisch und potentiometrisch)

Kuznetsova et al.; Russian Journal of Physical Chemistry; vol. 49; (1975); p. 261; ; p. 452, View in Reaxys

K-Salz : ν max

Okabayashi et al.; Bulletin of the Chemical Society of Japan; vol. 47; (1974); p. 1075, View in Reaxys

Komplex mit Py.: ΔH

Mashkovsky; Odinokov; Spectroscopy Letters; vol. 7; (1974); p. 271,273, 274, View in Reaxys

Na-Salz: Aequiva- Hoeiland; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phalentzleitf. (S. ses; vol. 70; (1974); p. 1180, View in Reaxys 1183) Butyrat: Grenzleit- Piekarski et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 71; (1974); p. 1524,1526, faehigkeit; 1527, View in Reaxys Diff.koeff. Natriumsalz: Viskositaetskoeffizient in H2O

Tamaki et al.; Bulletin of the Chemical Society of Japan; vol. 47; (1974); p. 384,385, View in Reaxys

K-Salz: Aequivalentleitfaehigkeit in wss. Dioxan

Piekarski et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 71; (1974); p. 1524,1526, 1527, View in Reaxys

K-Salz: F.: 404grad; Schmelzdiagramm mit Magnesiumbutyrat

Pochtakova et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 44; (1974); p. 241,229, View in Reaxys

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Na-Salz: F.: 330grad; Schmelzdiagramm mit Magnesiumbutyrat

Pochtakova et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 44; (1974); p. 241,229, View in Reaxys

Loesung: Bu4NBut: 1HNMR: chem. Verschiebung in Abhaengigkeit von Molalitaet, Temp. in Wasser

Lindenbaum; Levine; Journal of Solution Chemistry; vol. 3; (1974); p. 261, View in Reaxys

Mg-Salz: F.: 302grad; Schmelzdiagramme mit Natriumbutyrat u. Kaliumbutyrat (jeweils bin. Systeme)

Pochtakova et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 44; (1974); p. 241,229, View in Reaxys

Li-Salz: K

Kuznetsova et al.; Moscow University Chemistry Bulletin (English Translation); vol. 28; nb. 2; (1973); p. 21; ; p. 159, View in Reaxys

Na-Salz : SS-MS (Tab.II)

Buck; Hass; Analytical Chemistry; vol. 45; (1973); p. 2208,2209-2211, View in Reaxys

Ca-Salz : SS-MS (Tab.II)

Buck; Hass; Analytical Chemistry; vol. 45; (1973); p. 2208,2209-2211, View in Reaxys

Na-Salz: Molvol. in wss. Lsg.

Sakurai; Bulletin of the Chemical Society of Japan; vol. 46; (1973); p. 1596, View in Reaxys

Na-Salz: Rk. mit cis-Dichloraethylen, PdCl2

Yamaji,M. et al.; Bulletin of the Chemical Society of Japan; vol. 46; (1973); p. 90 - 93, View in Reaxys

Na-Salz: NaClLsg.: Assoziations-Gleichgew.

Stenius; Acta Chemica Scandinavica (1947-1973); vol. 27; (1973); p. 3435,3445, View in Reaxys

CH3-<CH2>7NH2-Salz: 1HNMR, cmc in CCl4 u. Benzol

Fendler et al.; Journal of Physical Chemistry; vol. 77; (1973); p. 1432,1434, 1435, View in Reaxys

Natriumsalz : Ver- Hoeiland; Acta Chemica Scandinavica (1947-1973); vol. 27; (1973); p. 2687,2689,2691, View in Reaxys halten waessriger Loesg. u. Druck : 1. Scheinbares Molvolumen Na-Salz: Rk. mit Cainelli et al.; Journal of the Chemical Society, Chemical Communications; (1973); p. 94, View in Reaxys 1) (i-Pr)2NLi, 2) 2,3-Dichlor-5,6-dicyanobenzochinon, Dehydrierung Na-Salz: DampStenius; Acta Chemica Scandinavica (1947-1973); vol. 27; (1973); p. 3435,3445, View in Reaxys fdruck der wss. Lsg. in Ggw. von NaCl; Aktivitaetskoeffizient; Assoziations-Gleichgew. System: SnCl4-nC3H7COOH in Benzene: dielektrische Eigenschaften, Einfluss

Marchenko; Pletnev; J. Gen. Chem. USSR (Engl. Transl.); vol. 43; (1973); p. 469,472,473,474, View in Reaxys

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des Loesungsmittels auf die Zus. d. Komplexverb. Na-Salz

Nagwekar; Muangnoicharoen; Journal of Pharmaceutical Sciences; vol. 61; (1972); p. 1439,1442, 1443, View in Reaxys; Hargreaves; Kresheck; Journal of Physical Chemistry; vol. 73; (1969); p. 3249, View in Reaxys

Kaliumsalz: F: 347grad

Michels; Ubbelohde; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1972); p. 1879, View in Reaxys

Caesiumsalz: F: 343grad

Michels; Ubbelohde; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1972); p. 1879, View in Reaxys

Lithiumsalz: F: 310grad

Michels; Ubbelohde; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1972); p. 1879, View in Reaxys

Natriumsalz: F: 251grad

Michels; Ubbelohde; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1972); p. 1879, View in Reaxys

Rubidiumsalz: F: 370grad

Michels; Ubbelohde; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1972); p. 1879, View in Reaxys

Li-Salz: Diss.Konst., Verteilung

Kuznetsova et al.; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 1637; ; p. 2880, View in Reaxys

(H3C-CH2-CH2CO2)4Cu2: MS (Tab. 1)

Khariton et al.; Doklady Chemistry; vol. 207; (1972); p. 1005,1006,1007,1008; Dokl. Akad. Nauk SSSR Ser. Khim.; vol. 207; (1972); p. 1369, View in Reaxys

Na-Salz, Phasenunters. (Netzebenenabst.)

Duruz; Ubbelohde; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 330; (1972); p. 1, View in Reaxys

Cs UO2 Alikhanova et al.; Optics and Spectroscopy; vol. 32; (1972); p. 290; ; p. 551, View in Reaxys (C3H7COO)3: optische Aktivitaet, Abs.-sp. Na+-Salz: Molal. Salz-Shift im NMR v. H2O u. CH3OH

Davies et al.; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 68; (1972); p. 686,687-690, View in Reaxys

Bird; Lomer; Acta Crystallographica, Section B: Structural Crystallography and Crystal Chemistry; vol. 28; Cu-Salz: Cu2+ (1972); p. 242,245, View in Reaxys (CH3-(CH2)2COO)2: gruen; paramagnetisch; aus Kupfercarbonatanhydrid, Buttersaeure in alkoholischer Lsg.; Roe: Krist. Strukt.: dimer; Elementarzelle; Bindungslaengen, Bindungswinkel Na-Salz, Phasenunters. (T, ΔH, D, Molvol., el. Leitf., η)

Duruz et al.; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 322; (1971); p. 281,283, View in Reaxys

Na-butyrat: Assoziationsgleichgewichte; Micellenbildung in wss. Loesung; Hydrolysekonstanten (Tab. 7, Tab. 10)

Stenius; Zilliacus; Acta Chemica Scandinavica (1947-1973); vol. 25; (1971); p. 2232, View in Reaxys

Na-Salz ; Verduennungswaerme

Lindenbaum; Journal of Physical Chemistry; vol. 74; (1970); p. 3027, View in Reaxys

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Na-Salz, Danielsson et al.; Suomen Kemistilehti B; vol. 43; (1970); p. 209,210, 211, View in Reaxys Na(C4H7O2): 1HNMR (Relaxationszeit) Addukt : ZrCl4 * 2 Ludwig; Schwartz; Inorganic Chemistry; vol. 9; (1970); p. 607, View in Reaxys n-C3H7COOH; B.: ZrCl4 + C3H7COOH. Ba-Salz: Pyrolyse Noszko et al.; Radiochemical and Radioanalytical Letters; vol. 5; (1970); p. 265,272, View in Reaxys m.<1-14C>-Baacetat: Produktvertlg. Mg-Salz Matsuda et al.; Kogyo Kagaku Zasshi; vol. 73; (1970); p. 1007; Chem.Abstr.; vol. 73; nb. 87983; (1970), Mg(OCOC3H7)2: View in Reaxys aus Buttersaeure, MgO, Bzl.; F: 296.8grad Na-Salz : F= 330grad ; Ternaeres System mit NaNO3 u. NaNO2 ( Eutektische Punkte )

Sokolov et al.; Russian Journal of Inorganic Chemistry (Translation of Zhurnal Neorganicheskoi Khimii); vol. 15; (1970); p. 721,723; ; p. 1405, View in Reaxys

Na-Salz: F: 256grad; Schmelzwaerme; Schmelzentropie; Klaerpunkt (Waerme, Entropie)

Ubbelohde et al.; Nature (London, United Kingdom); vol. 228; (1970); p. 51, View in Reaxys

mol. Verb. PyriKrupatkin; Rozhentsova; Russian Journal of Physical Chemistry; vol. 44; (1970); p. 575; ; p. 1036, din-Buttersaeure View in Reaxys (1:2): Phasengleichgewicht Buttersaeure-Pyridin-H2O Na-Salz (S. 1222, King; Journal of Physical Chemistry; vol. 73; (1969); p. 1220,1222,1223, View in Reaxys 1223) NH4-Salz : Addi- Lindenberg; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 364; (1969); p. 20, View in Reaxys tionsverb. m. NH3 Li-Salz: Schmelzdiagramm des binaeren Systems mit LiSCN: Eutekt. Pkte.

Sokolov; Dmitrevskaya; Russian Journal of Inorganic Chemistry (Translation of Zhurnal Neorganicheskoi Khimii); vol. 14; (1969); p. 148, View in Reaxys

Na-Salz : Rk. m. Jansson; Leimu; Suomen Kemistilehti B; vol. 42; (1969); p. 6, View in Reaxys Hexyl-chlormethylaether zu Buttersaeure-hexyloxymethylester , Dihexylformal u. Hexanol Na-Salz: Sokolov; Dmitrevskaya; Russian Journal of Inorganic Chemistry (Translation of Zhurnal Neorganicheskoi SchmelzdiaKhimii); vol. 14; (1969); p. 148, View in Reaxys gramm des binaeren Systems mit NaSCN: Eutekt. Pkte.-->Pochtakova in Tezisy Dokladov XIX Nauchnoi Konferentsii Smolensko-

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go Meditsinskogo Instituta zitiert in Na-Salz: krit. Micellenkonz.

Durand; Cordier; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 65; (1968); p. 533, View in Reaxys

Na-Salz (S. 860, 861, 862, 865)

Kunimitsu et al.; Journal of Physical Chemistry; vol. 72; (1968); p. 856, View in Reaxys

K-Salz: Schallmessungen in wss. Lsg.

Zana; Yeager; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 65; (1968); p. 467, View in Reaxys

K-Salz : Rk. m. Atkinson et al.; Journal of the American Chemical Society; vol. 90; (1968); p. 498, View in Reaxys D2O bei 150grad zu (α,α-D2)Buttersaeure Na-Salz : Rk. m. Atkinson et al.; Journal of the American Chemical Society; vol. 90; (1968); p. 498, View in Reaxys D2O bei 150grad zu (α,α-D2)Buttersaeure Na-Salz : Rk. m. N-Butyl-chlormethylaether in wss. Lsg. zu Buttersaeure-n-butoxymethylester , Formaldehyd-din-butylacetal , nButanol , Formaldehyd

Jansson et al.; Suomen Kemistilehti B; vol. 41; (1968); p. 281, View in Reaxys

Na-Salz: Kin. d. Rk. m. Phenacylbromid

Okamoto et al.; Bulletin of the Chemical Society of Japan; vol. 40; (1967); p. 1905,1908, View in Reaxys

Komplex mit Pfer- Sigman; Journal of Biological Chemistry; vol. 242; (1967); p. 3815,3818, View in Reaxys deleberalkoholdehydrogenase: K Na-Salz Benjamin; Journal of Physical Chemistry; vol. 70; (1966); p. 3790,3794, View in Reaxys C4H7O2Na: Molvolumen bei 25grad; Partielles Molvolumen in W. (monomer) bei 30grad Anilid: F: 146grad

Goryaev et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 38; (1965); p. 2622,2563, View in Reaxys

Ag-Salz: IR

Kirby et al.; Journal of the American Oil Chemists' Society; vol. 42; (1965); p. 437,440, View in Reaxys

Pb-Salz: IR

Kirby et al.; Journal of the American Oil Chemists' Society; vol. 42; (1965); p. 437,440, View in Reaxys

Komplex mit SO3 (C4H8O2)3*SO3: Dipolmoment: 6.54 D; spez. Leitfaehigkeit; Dielektrizitaetskonst. bei 26grad

Paul et al.; Indian Journal of Chemistry; vol. 3; (1965); p. 239, View in Reaxys

Komplex mit SO3 (C4H8O2)2*SO3: D28: 1.2400; Molvolumen; spez. Leitfaehigkeit; Dielektrizitaetskonst. bei 26grad

Paul et al.; Indian Journal of Chemistry; vol. 3; (1965); p. 239, View in Reaxys

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K-Salz

Khomutov et al.; Russian Journal of Physical Chemistry; vol. 37; (1963); p. 93; ; p. 189, View in Reaxys; Hertz; Zeidler; Berichte der Bunsen-Gesellschaft; vol. 68; (1964); p. 821,830, 833, View in Reaxys

K-Salz, IR-Sp., solid and aq.

Gotoh; Takenaka; Nippon Kagaku Zasshi; vol. 84; (1963); p. 392; Chem.Abstr.; vol. 59; nb. 7080b; (1963), View in Reaxys

Ag-Salz, IR-Sp., solid and aq.

Gotoh; Takenaka; Nippon Kagaku Zasshi; vol. 84; (1963); p. 392; Chem.Abstr.; vol. 59; nb. 7080b; (1963), View in Reaxys

Li-Salz, IR-Sp., solid and aq.

Gotoh; Takenaka; Nippon Kagaku Zasshi; vol. 84; (1963); p. 392; Chem.Abstr.; vol. 59; nb. 7080b; (1963), View in Reaxys

Na-Salz, IR-Sp., solid and aq.

Gotoh; Takenaka; Nippon Kagaku Zasshi; vol. 84; (1963); p. 392; Chem.Abstr.; vol. 59; nb. 7080b; (1963), View in Reaxys

4-Jod-phenacylester: F: 82.6grad

Stodola; Microchemical Journal; vol. 7; (1963); p. 389,390-399; Chem.Abstr.; vol. 60; nb. 11934c; (1964), View in Reaxys

4-Brom-phenacylester: F: 63.7grad

Stodola; Microchemical Journal; vol. 7; (1963); p. 389,390-399; Chem.Abstr.; vol. 60; nb. 11934c; (1964), View in Reaxys

4-Chlor-phenacylester: F: 56.0grad

Stodola; Microchemical Journal; vol. 7; (1963); p. 389,390-399; Chem.Abstr.; vol. 60; nb. 11934c; (1964), View in Reaxys

Methylester: Best. Gehrke; Goerlitz; Analytical Chemistry; vol. 35; (1963); p. 76,79, View in Reaxys in Fettsaeuregemischen Na-Salz: monoklin; Raumgruppe: A2/α; Z = 8

Segerman; Acta Crystallographica; vol. 16; (1963); p. A76, View in Reaxys

K-Salz: elektr. Leitfaehigkeit in W. zwischen 25grad u. 225grad

Ellis; Journal of the Chemical Society; (1963); p. 2299,2302, View in Reaxys

S-<Naphthyl-(1)- Snobl et al.; Collection of Czechoslovak Chemical Communications; vol. 28; (1963); p. 436,437, methyl>-isothiuro- View in Reaxys nium-Salz: F: 143grad; Roentgenograph. Identif. Verb. m. SO3

Paul et al.; Journal of the Indian Chemical Society; vol. 39; (1962); p. 297, View in Reaxys

Dicyclohexylamin- Bestmann,H.J.; Schulz,H.; Chemische Berichte; vol. 95; (1962); p. 2921 - 2927, View in Reaxys salz: F: 110-112grad Natriumsalz: Intensitaeten charakteristischer IRBanden

Flett,M.S.C.; Spectrochimica Acta; vol. 18; (1962); p. 1537 - 1556, View in Reaxys

Calciumsalz: Adsorption an verschiedenen Anionenaustauschern

Dawydow; Lisowina; Zhurnal Fizicheskoi Khimii; vol. 36; (1962); p. 1993; ; p. 1072, View in Reaxys

Buttersaeure-<4(4-nitro-phenylazo)-phenylester>: F: 96grad (Me.)

Kupryszewski; Kazmierczak; Roczniki Chemii; vol. 36; (1962); p. 1325; Chem.Abstr.; vol. 59; nb. 6249, View in Reaxys

Na-Salz: Rk. mit Normant; Angelo; Bulletin de la Societe Chimique de France; (1962); p. 814, View in Reaxys 1. Na, Naphthalin, THF, Kochen, 2. kalten Rk.-gemisch., C6H5CH2Cl, -> α-Aeth-

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yl-hydrozimtsaeure (Ausbeute 30percent) Kaliumsalz C4H7O2K: F: 404grad

Sokolow et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 1051,971; Chem.Abstr.; nb. 20593; (1961), View in Reaxys

Lithiumsalz C4H7O2Li: F: 330grad

Sokolow et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 1051,971; Chem.Abstr.; nb. 20593; (1961), View in Reaxys

Natriumsalz C4H7O2Na: F: 330grad

Sokolow et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 1051,971; Chem.Abstr.; nb. 20593; (1961), View in Reaxys

4-Nitro-phenacylester: Colorimetr. Best.

Bartos; Talanta; vol. 8; (1961); p. 556; Chem.Abstr.; nb. 24393; (1961), View in Reaxys

2-Chlor-aethyl-es- Oette; Ahrens; Analytical Chemistry; vol. 33; (1961); p. 1847, View in Reaxys ter: gaschromatogr. Best. Kaliumbutyrat KC4H7O2: magnetische Suszeptibilitaet

Sriraman; Thiruvengadathan; Bulletin of the Chemical Society of Japan; vol. 34; (1961); p. 1560, View in Reaxys

Natriumbutyrat Sriraman; Thiruvengadathan; Bulletin of the Chemical Society of Japan; vol. 34; (1961); p. 1560, NaC4H7O2: mag- View in Reaxys netische Suszeptibilitaet Bariumbutyrat Sriraman; Thiruvengadathan; Bulletin of the Chemical Society of Japan; vol. 34; (1961); p. 1560, Ba(C4H7O2)2: View in Reaxys magnetische Suszeptibilitaet Calciumbutyrat Sriraman; Thiruvengadathan; Bulletin of the Chemical Society of Japan; vol. 34; (1961); p. 1560, Ca(C4H7O2)2: View in Reaxys magnetische Suszeptibilitaet Strontiumbutyrat Sriraman; Thiruvengadathan; Bulletin of the Chemical Society of Japan; vol. 34; (1961); p. 1560, Sr(C4H7O2)2: View in Reaxys magnetische Suszeptibilitaet Natriumsalz: Entmischung d. ternaeren Systems m. Kalium- u. Natriumrhodanid; Entmischung d. ternaeren Systems m. KNO3 u. NaNO3

Sokolow et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 1051,971; Chem.Abstr.; nb. 20593; (1961), View in Reaxys

Lithiumsalz: Entmischung d. ternaeren Systems m. Natrium- u. Lithiumrhodanid; Entmischung d. Systems m. LiNO3 + NaNO3 und LiNO3 + KNO3

Sokolow et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 1051,971; Chem.Abstr.; nb. 20593; (1961), View in Reaxys

Phenylphenacylester: F: 82grad

Heyns; Blazejewicz; Tetrahedron; vol. 9; (1960); p. 67,73, View in Reaxys

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4-Butyryl-aminoa- Kinoshita; Nakajima; Chemical and Pharmaceutical Bulletin; vol. 8; (1960); p. 56, View in Reaxys zobenzol: F: 180grad NH-Salz: Papier- Howe; Journal of Chromatography; vol. 3; (1960); p. 389,390-405; Chem.Abstr.; vol. 55; nb. 7267; (1961), chromatogr. IsoView in Reaxys lierung und Identifizierung Na-Salz: aus 14CO2, Propylmagnesiumbromid, als 1-14Cmarkiertes Praeparat

Okubo; Goto; Nippon Kagaku Zasshi; vol. 81; (1960); p. 1132,1133-1136; Chem.Abstr.; nb. 3342; (1962), View in Reaxys

Na-Salz Ssokolow; Potschtakowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 1401,1429; Chem.Abstr.; C4H7O2Na: nb. 23685; (1960), View in Reaxys Thermische Analyse d. Systems m. CH3CO2Na; Eutektikum bei 266grad, 33.5percent und bei 250grad, 69percent C4H7O2Na K-Salz C4H7O2K: Ssokolow; Potschtakowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 1401,1429; Chem.Abstr.; Thermische Ana- nb. 23685; (1960), View in Reaxys lyse d. Systems m. CH3CO2K, Eutektikum bei 273grad, 85.5percent CH3CO2K; Therm. Analyse d. Systems m. CH3CO2Na (Tab. 2); Therm. Analyse d. Systems m. C3H7CO2Na, CH3CO2Na u. CH3CO2K (Fig. 1, 2, 3) Lithiumsalz Zindrik; Ssokolow; J. Gen. Chem. USSR (Engl. Transl.); vol. 28; (1958); p. 1728,1775; Chem.Abstr.; nb. C4H7O2*Li: 19414; (1958), View in Reaxys Schmelzdiagramm mit NaNO3; Eutektikum bei 298grad mit 91 Molpercent tributyrato-dioxo- Ferrari et al.; Gazzetta Chimica Italiana; vol. 87; (1957); p. 1203,1207, View in Reaxys uranic acid-potassium-salt; Further Data see Handbook (Crystal phase, Crystal system, Density of the crystal) as anilide (mp: 96.1-96.4 degree )

de Jonge et al.; Recueil des Travaux Chimiques des Pays-Bas; vol. 75; (1956); p. 5,10, View in Reaxys

as 4-phenylazophenacyl ester (mp: 98-99 degree )

Ikeda et al.; Analytical Chemistry; vol. 26; (1954); p. 1228, View in Reaxys

as S-<4-nitroMOMOSE; TANAKA; Pharmaceutical bulletin; vol. 2; nb. 2; (1954); p. 152 - 154, View in Reaxys benzyl>-isothiuro-

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2017-08-01 04:43:04

nium salt (mp: 138 degree ) as S-<2,4-dinitro- MOMOSE; TANAKA; Pharmaceutical bulletin; vol. 2; nb. 2; (1954); p. 152 - 154, View in Reaxys benzyl>-isothiuronium salt (mp: 134 degree ) <pentaammineLinhard; Rau; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 271; (1953); p. 121,124, butyrato cobalt View in Reaxys; Linhard; Weigel; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 264; (1951); p. (III)>-diperchlo321,326, View in Reaxys rate; Further Data see Handbook (Absorption maxima, Solubility) <cis-tetraammine- Linhard; Weigel; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 264; (1951); p. 321,326, dibutyrato cobalt View in Reaxys (III)>-perchlorate; Further Data see Handbook (Absorption maxima) <trans-tetraammine-dibutyrato cobalt (III)>-perchlorate; Further Data see Handbook (Absorption maxima)

Linhard; Weigel; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 264; (1951); p. 321,326, View in Reaxys

as 4-phenyl-phenacyl ester (mp: 83.5-84 degree ):

Owen; Sultanbawa; Journal of the Chemical Society; (1949); p. 3104, View in Reaxys

cobalt-butyrate (cis-complex); Further Data see Handbook (Solubility)

Linhard; Weigel; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 260; (1949); p. 67,80, View in Reaxys

cobalt-butyrate (trans-complex); Further Data see Handbook (Solubility)

Linhard; Weigel; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 260; (1949); p. 67,80, View in Reaxys

as 4-phenyl-phenacyl ester (mp: 82 degree ):

Barger; Martin; Mitchell; Journal of the Chemical Society; (1938); p. 1688, View in Reaxys; Morton et al.; Journal of the American Chemical Society; vol. 67; (1945); p. 2228, View in Reaxys

as N.N'-dibutyrylnaphthylenediamine-(1.5) (mp: 269 degree ) or N.N'-dibutyrylbenzidine (mp: 312 degree ):

Buu-Hoi; Bulletin de la Societe Chimique de France; vol. <5>12; (1945); p. 590,592, View in Reaxys

1:1 addition com- Ssemischin; Zhurnal Obshchei Khimii; vol. 13; (1943); p. 633,634; Chem.Abstr.; (1945); p. 456, pound with hydra- View in Reaxys zine (mp: 50.2 degree ); Further Data see Handbook lithium butyrate; Further Data see Handbook (IR Spectrum)

Duval; Lecomte; Douville; Annales de Physique (Paris, France); vol. <11> 17; (1942); p. 5,42, 71, View in Reaxys

magnesium buty- Duval; Lecomte; Douville; Annales de Physique (Paris, France); vol. <11> 17; (1942); p. 5,42, 71, rate; Further Data View in Reaxys

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2017-08-01 04:43:04

see Handbook (IR Spectrum) as 4-phenyl-phenacyl ester (mp: 97 degree ):

Koegl; Sparenburg; Recueil des Travaux Chimiques des Pays-Bas; vol. 59; (1940); p. 1180,1186, 1197, View in Reaxys; Drake; Bronitsky; Journal of the American Chemical Society; vol. 52; (1930); p. 3715,3716, 3719, View in Reaxys

as N.N'-dibutyryl- Sah; Recueil des Travaux Chimiques des Pays-Bas; vol. 59; (1940); p. 1029,1034, View in Reaxys hydrazine (mp: 167-168 degree ): as S-<4-chlorobenzyl>-thiuronium salt (mp: 139 degree ):

Dewey; Sperry; Journal of the American Chemical Society; vol. 61; (1939); p. 3252, View in Reaxys

as picrate of 2Brown; Campbell; Journal of the Chemical Society; (1937); p. 1699, View in Reaxys propyl-benzimidazole (mp: 124 degree ): as S-benzylthiuronium salt (mp: 146 degree ):

Donleavy; Journal of the American Chemical Society; vol. 58; (1936); p. 1004, View in Reaxys

aluminium butyPatent; Stickstoffduenger,A.G.; DE695443; (1936); DRP/DRBP Org.Chem., View in Reaxys; Ostwald; Rierate; Further Data del; Kolloid-Zeitschrift; vol. 70; (1935); p. 71, View in Reaxys see Handbook (Preparation, Transport phenomena) compound with deoxycholic acid; Further Data see Handbook

Sobotka; Goldberg; Biochemical Journal; vol. 26; (1932); p. 555,567, View in Reaxys; Wieland; Sorge; Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie; vol. 97; (1916); p. 1,20, 27, View in Reaxys; Go; Kratky; Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie; vol. <B> 26; (1934); p. 439,442, View in Reaxys

as 4-iodo-phenac- Koegl; Erxleben; Justus Liebigs Annalen der Chemie; vol. 484; (1930); p. 65,80, View in Reaxys; Judefind; yl ester (mp: Reid; Journal of the American Chemical Society; vol. 42; (1920); p. 1049, View in Reaxys; Moses; Reid; 81.4-81.5 deJournal of the American Chemical Society; vol. 54; (1932); p. 2101, View in Reaxys gree ): <Co(NH3)4(NO2 )2>C4H7O2; Further Data see Handbook (Solubility)

Broensted; Delbanco; Volqvartz; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 162; (1932); p. 133, View in Reaxys

lead butyrate; Further Data see Handbook (Crystal phase)

Trillat; Annales de Physique (Paris, France); vol. <10>; nb. 6; (1926); p. 76, View in Reaxys

copper butyrate; Further Data see Handbook (UV/VIS Spectrum)

French; Lowry; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 106; (1924); p. 496; Chem. Zentralbl.; vol. 96; nb. I; (1925); p. 601, View in Reaxys

zinc butyrate; Fur- van Epps; Reid; Journal of the American Chemical Society; vol. 38; (1916); p. 2125, View in Reaxys ther Data see Handbook (Chemical Behaviour) lead butyrate; Petersen; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 20; (1914); p. 330, Further Data see View in Reaxys Handbook (Chemical Behaviour) silver butyrate; Further Data see Handbook

Denham; Woodhouse; Journal of the Chemical Society; vol. 103; (1913); p. 1866, View in Reaxys

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(Chemical Behaviour) magnesium buty- Wright; Journal of the Chemical Society; vol. 103; (1913); p. 529; Journal of the Chemical Society; vol. 105; rate; Further Data (1914); p. 670, View in Reaxys; Hantzsch; Scharf; Chemische Berichte; vol. 46; (1913); p. 3580, see Handbook View in Reaxys (UV/VIS Spectrum) barium butyrate; Further Data see Handbook (UV/VIS Spectrum, Chemical Behaviour)

Wright; Journal of the Chemical Society; vol. 103; (1913); p. 529; Journal of the Chemical Society; vol. 105; (1914); p. 670, View in Reaxys; Neuberg; Tir; Biochemische Zeitschrift; vol. 32; (1911); p. 329, View in Reaxys; Hantzsch; Scharf; Chemische Berichte; vol. 46; (1913); p. 3580, View in Reaxys

calcium butyrate; Further Data see Handbook (UV/VIS Spectrum, Chemical Behaviour)

Wright; Journal of the Chemical Society; vol. 103; (1913); p. 529; Journal of the Chemical Society; vol. 105; (1914); p. 670, View in Reaxys; Neuberg; Tir; Biochemische Zeitschrift; vol. 32; (1911); p. 329, View in Reaxys; Soehngen; Recueil des Travaux Chimiques des Pays-Bas; vol. 29; (1910); p. 251, View in Reaxys; Hantzsch; Scharf; Chemische Berichte; vol. 46; (1913); p. 3580, View in Reaxys

copper butyrate; Further Data see Handbook (Solubility)

Pickering; Journal of the Chemical Society; vol. 101; (1912); p. 175; Journal of the Chemical Society; vol. 101; (1912); p. 1628, View in Reaxys

hexaquochrombu- Werner; Chemische Berichte; vol. 41; (1908); p. 3454, View in Reaxys tyrate; Further Data see Handbook (Preparation) as salt of benzyla- Boudet Bl.; 1948 391, View in Reaxys mine (mp: 54-55 degree ): Purification (1) References Demeyer; Henderickx; Bulletin des Societes Chimiques Belges; vol. 73; (1964); p. 615, View in Reaxys; Langner; Angewandte Chemie; vol. 77; (1965); p. 95, View in Reaxys; CLEMENT; BEZARD; Comptes rendus hebdomadaires des séances de l'Académie des sciences; vol. 253; (1961); p. 564 - 566, View in Reaxys; Churacek; Microchimica Acta; (1961); p. 65,66-69; Chem.Abstr.; nb. 24394; (1961), View in Reaxys; Hunter et al.; Analytical Chemistry; vol. 32; (1960); p. 682, View in Reaxys Melting Point (17) 1 of 17

Melting Point [°C]

-6 - -3

Chang, Fei; Kim, Hakwon; Lee, Byeongno; Park, Sungho; Park, Jaiwook; Tetrahedron Letters; vol. 51; nb. 32; (2010); p. 4250 - 4252, View in Reaxys 2 of 17

Melting Point [°C]

-7.9

Schneider; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 22; (1897); p. 233, View in Reaxys; Patent; UNIVERSITE DE MONTREAL; THE GOVERNING COUNSIL OF THE UNIVERSITY OF TORONTO; WO2008/58366; (2008); (A1) English, View in Reaxys 3 of 17

Melting Point [°C]

-94

Patent; Zaworotko, Michael J.; Moulton, Brian; Rodriguez-Hornedo, Nair; US2003/224006; (2003); (A1) English, View in Reaxys 4 of 17

Melting Point [°C]

-5.55

Timmermans; Bulletin des Societes Chimiques Belges; vol. 36; (1927); p. 507; Chem. Zentralbl.; vol. 99; nb. I; (1928); p. 27, View in Reaxys; Radwan; Hanna; Journal of Chemical and Engineering Data; vol. 21; (1976); p. 285,286,287,288, View in Reaxys 5 of 17

Melting Point [°C]

-5

Timrot et al.; High Temperature; vol. 14; (1976); p. 1068; ; p. 1192, View in Reaxys 6 of 17

Melting Point [°C]

-7

Strieter; Templeton; Acta Crystallographica; vol. 15; (1962); p. 1240,1243, View in Reaxys

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2017-08-01 04:43:04

7 of 17

Melting Point [°C]

-5.26

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys 8 of 17

Comment (Melting Point)

Melting point:Erstarrungspunkt zwischen 1 atm (-5,50grad) und 986 atm (+13,00grad).

Deffet; Bulletin des Societes Chimiques Belges; vol. 44; (1935); p. 69, View in Reaxys 9 of 17

Melting Point [°C]

-5.5

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys 10 of 17

Melting Point [°C]

-6.55

Grindley; Bury; Journal of the Chemical Society; (1929); p. 682, View in Reaxys 11 of 17

Melting Point [°C]

-5.7

Parks; Anderson; Journal of the American Chemical Society; vol. 48; (1926); p. 1508, View in Reaxys 12 of 17

Melting Point [°C]

-4.7 - -4.65

English; Turner; Journal of the Chemical Society; vol. 107; (1915); p. 777, View in Reaxys 13 of 17

Melting Point [°C]

-3.12

Faucon; Annales de Chimie (Cachan, France); vol. <8> 19; (1910); p. 85, View in Reaxys 14 of 17

Melting Point [°C]

-4.5 - -2

Zander; Justus Liebigs Annalen der Chemie; vol. 224; (1884); p. 81, View in Reaxys 15 of 17

Melting Point [°C]

-19

Linnemann; Justus Liebigs Annalen der Chemie; vol. 160; (1871); p. 241; Justus Liebigs Annalen der Chemie; vol. 192; (1878); p. 69, View in Reaxys 16 of 17

Melting Point [°C]

-2 - 2

Linnemann; Justus Liebigs Annalen der Chemie; vol. 160; (1871); p. 241; Justus Liebigs Annalen der Chemie; vol. 192; (1878); p. 69, View in Reaxys 17 of 17

Dreisbach; Advances in Chemistry Series; p. 439, View in Reaxys

Boiling Point (64) Boiling Point [°C] Pressure (Boiling Point) [Torr]

References

164

Hara, Takeshi; Kyuka, Ayumi; Shimizu, Hironori; Chemistry and Biodiversity; vol. 12; nb. 2; (2015); p. 248 - 258, View in Reaxys

163.5

Yang, Baibing; Xu, Chunming; Zhao, Suoqi; Hsu, Chang Samuel; Chung, Keng H.; Shi, Quan; Science China Chemistry; vol. 56; nb. 7; (2013); p. 848 - 855, View in Reaxys

163

Smith, David; Chippendale, Thomas W.E.; Spanel, Patrik; International Journal of Mass Spectrometry; vol. 303; nb. 2-3; (2011); p. 81 - 89, View in Reaxys

164.84

Tian, Senlin; Liu, Lian; Ning, Ping; Journal of Solution Chemistry; vol. 39; nb. 4; (2010); p. 457 - 472, View in Reaxys

162

Vereshchagin,L.I. et al.; Zhurnal Organicheskoi Khimii; vol. 11; nb. 2; (1975); p. 292 295,285 - 287, View in Reaxys; Krost, Kenneth J.; Pellizzari, Edo D.; Walburn, Stephen G.; Hubbard, Sarah A.; Analytical Chemistry; vol. 54; nb. 4; (1982); p. 810 - 817, View in Reaxys; Patent; SUNTORY FLOWERS LIMITED; US2009/119801; (2009); (A1) English, View in Reaxys

164

Wright; Akhtar; Journal of the Chemical Society [Section] B: Physical Organic; (1970); p. 151,152-153, View in Reaxys; Trabue, Steven L.; Scoggin, Kenwood D.; Li, Hong; Burns, Robert; Xin, Hongwei; Environmental Science and Technology; vol. 42; nb. 10; (2008); p. 3745 - 3750, View in Reaxys

83 - 84

Svetlakov; Nikitin; Nikolaeva; Russian Journal of Organic Chemistry; vol. 43; nb. 5; (2007); p. 771 - 772, View in Reaxys

163.54

760.014

Kirbaslar, S. Ismail; Sahin, Selin; Bilgin, Mehmet; Journal of Chemical Thermodynamics; vol. 39; nb. 2; (2007); p. 284 - 290, View in Reaxys

25/428

2017-08-01 04:43:04

163.54

0.760014

Kirbaslar, S. Ismail; Journal of Chemical Thermodynamics; vol. 38; nb. 6; (2006); p. 696 - 700, View in Reaxys

163.51

760.014

Bilgin, Mehmet; Journal of Chemical Thermodynamics; vol. 38; nb. 12; (2006); p. 1634 1639, View in Reaxys

161

Hashemi, Mohammed M.; Ghazanfari, Dadkhoda; Ahmadibeni, Yousef; Karimi-Jaberi, Zahed; Ezabadi, Ali; Synthetic Communications; vol. 35; nb. 8; (2005); p. 1103 1107, View in Reaxys

162 - 164

Bratulescu, George; Revue Roumaine de Chimie; vol. 50; nb. 3; (2005); p. 161 - 163, View in Reaxys

164.35

Munoz, Laura A. L.; Kraehenbuehl, M. Alvina; Journal of Chemical and Engineering Data; vol. 46; nb. 1; (2001); p. 120 - 124, View in Reaxys

163.27

Zudkevitch; Lindrud; Chu; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 393 - 397, View in Reaxys

6-8

163.2

Webb, Kevin S.; Ruszkay, Stephen J.; Tetrahedron; vol. 54; nb. 3-4; (1998); p. 401 410, View in Reaxys Govindarajan; Sabarathinam; Journal of Chemical and Engineering Data; vol. 42; nb. 2; (1997); p. 402 - 408, View in Reaxys

Olah; Wu; Synthesis; nb. 5; (1991); p. 407 - 408, View in Reaxys

65 - 66

Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 - 462, View in Reaxys

69.53

15.001

Ambrose, D.; Ghiassee, N. B.; Journal of Chemical Thermodynamics; vol. 19; nb. 5; (1987); p. 505 - 520, View in Reaxys

163.72

760

Ambrose, D.; Ghiassee, N. B.; Journal of Chemical Thermodynamics; vol. 19; nb. 5; (1987); p. 505 - 520, View in Reaxys

160 - 162

690

Tkacheva, G. D.; Suvorov, B. V.; Journal of Organic Chemistry USSR (English Translation); (1985); p. 1173 - 1177; Zhurnal Organicheskoi Khimii; vol. 21; nb. 6; (1985); p. 1289 - 1293, View in Reaxys

159 - 162

Costisella, Burkhard; Gross, Hans; Tetrahedron; vol. 38; nb. 1; (1982); p. 139 - 145, View in Reaxys

130 - 140

Samaddar, Haraprasad; Banerjee, Amalendu; Journal of the Indian Chemical Society; vol. 59; nb. 7; (1982); p. 905 - 906, View in Reaxys

Kaulen; Schaefer; Synthesis; (1979); p. 513, View in Reaxys

164.1

Suzuki et al.; Chemical Engineering Science; vol. 33; (1978); p. 271,273, View in Reaxys

163

Chumachenko,T.K. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 40; nb. 4; (1970); p. 846 - 854,826 - 832, View in Reaxys; Satchell; Journal of the Chemical Society; (1960); p. 1752,1754, View in Reaxys; Ogata; Sugimoto; Journal of Organic Chemistry; vol. 43; (1978); p. 3684,3687, View in Reaxys; Seinalow; Magerramowa; Azerbaidzhanskii Khimicheskii Zhurnal; vol. 2; (1965); p. 34,35; Chem.Abstr.; vol. 63; nb. 13131; (1965), View in Reaxys; Seinalew; Aliew; Azerbaidzhanskii Khimicheskii Zhurnal; vol. 1; (1964); p. 89,93; Chem.Abstr.; vol. 63; nb. 1711; (1965), View in Reaxys

159 - 160

Ayyangar et al.; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry; vol. 16; (1978); p. 555, View in Reaxys

94 - 97

Suhara; Yukagaku; vol. 25; (1976); p. 75,77; Chem.Abstr.; vol. 85; nb. 32375x, View in Reaxys

163.55

Radwan; Hanna; Journal of Chemical and Engineering Data; vol. 21; (1976); p. 285,286,287,288, View in Reaxys

162 - 163

Paul et al.; Journal of the Indian Chemical Society; vol. 46; (1969); p. 819,823, View in Reaxys; Maskill; Whiting; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1976); p. 1462,1469, View in Reaxys

163 - 164

Radecki; Kaczmarek; Journal of Chemical and Engineering Data; vol. 20; (1975); p. 378,379,380, View in Reaxys; Lande; Kochi; Journal of the American Chemical Society; vol. 90; (1968); p. 5196,5198,5206, View in Reaxys

159 - 159.5

Schrumpf; Klein; Chemische Berichte; vol. 106; (1973); p. 266,278, View in Reaxys

26/428

2017-08-01 04:43:04

Kokot; Jasinski; Roczniki Chemii; vol. 46; (1972); p. 1335,1336, 1339, View in Reaxys 74 - 78

Shaw; Knutson; Journal of Organic Chemistry; vol. 36; (1971); p. 1151, View in Reaxys

163.5

Bolotov,B.A. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 40; nb. 4; (1970); p. 823 827,802 - 806, View in Reaxys

160 - 162

Kachniaschwili et al.; Zhurnal Organicheskoi Khimii; vol. 2; (1966); p. 62,59, View in Reaxys

161 - 163

Suga et al.; Bulletin of the Chemical Society of Japan; vol. 38; (1965); p. 893,895, View in Reaxys

159 - 170

Babel; Proskuryakov; J. Appl. Chem. USSR (Engl. Transl.); vol. 38; (1965); p. 1085,1064,1067, View in Reaxys

162 - 162.5

760

Gotoh; Takenaka; Nippon Kagaku Zasshi; vol. 84; (1963); p. 392; Chem.Abstr.; vol. 59; nb. 7080b; (1963), View in Reaxys

160 - 165

Chiang; Li; Huaxue Xuebao; vol. 28; (1962); p. 379; Chem.Abstr.; vol. 59; nb. 12636; (1963), View in Reaxys

162.3

Schelesnjak; Zhurnal Fizicheskoi Khimii; vol. 35; (1961); p. 322; engl. Ausgabe; p. 155, View in Reaxys

162.5 - 163

Kawano; Nippon Kagaku Zasshi; vol. 81; (1960); p. 1652,1653; Chem.Abstr.; nb. 7040; (1961), View in Reaxys

163.25

760

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

164.05

760

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys

70.8

Biltz; Fischer; Wuennenberg; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 151; (1930); p. 18, View in Reaxys

162

742

Kailan; Schachner; Monatshefte fuer Chemie; vol. 52; (1929); p. 23, View in Reaxys

163.54 - 163.56

760

Timmermans; Bulletin des Societes Chimiques Belges; vol. 36; (1927); p. 507; Chem. Zentralbl.; vol. 99; nb. I; (1928); p. 27, View in Reaxys

162.45

760

Lecat; Recueil des Travaux Chimiques des Pays-Bas; Ann.Soc.scient.Bruxelles; vol. 47 I; (1927); p. 15,153, View in Reaxys

156 - 157

685

Bhide; Watson; Journal of the Chemical Society; (1927); p. 2102, View in Reaxys

163.5

757

Thomas; Sudborough; Journal of the Chemical Society; vol. 101; (1912); p. 324, View in Reaxys

0.1

Faucon; Annales de Chimie (Cachan, France); vol. <8> 19; (1910); p. 135, View in Reaxys

18.2

0.7

Faucon; Annales de Chimie (Cachan, France); vol. <8> 19; (1910); p. 135, View in Reaxys

58.7

9.5

Faucon; Annales de Chimie (Cachan, France); vol. <8> 19; (1910); p. 135, View in Reaxys

163.1

762.1

Schmidt; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 7; (1891); p. 458, View in Reaxys

63.5 - 161.8

12.5 - 750

Ramsay; Young; Chemische Berichte; vol. 19; (1886); p. 2110, View in Reaxys; Schmidt; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 7; (1891); p. 458, View in Reaxys

162.4 161.5 - 162.5

Zander; Justus Liebigs Annalen der Chemie; vol. 224; (1884); p. 81, View in Reaxys 753.2

162.5

Bruehl; Justus Liebigs Annalen der Chemie; vol. 203; (1880); p. 24, View in Reaxys Linnemann; Justus Liebigs Annalen der Chemie; vol. 160; (1871); p. 241; Justus Liebigs Annalen der Chemie; vol. 192; (1878); p. 69, View in Reaxys

163.2

748.7

Lieben; Rossi; Justus Liebigs Annalen der Chemie; vol. 158; (1871); p. 170, View in Reaxys

150.7

507.5

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

27/428

2017-08-01 04:43:04

136.77

315.5

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

112.57

123.8

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

101.32

75.9

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

90.92

47.2

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

Refractive Index (59) Refractive Index Wavelength (Refractive Index) [nm]

Temperature (Refractive Index) [°C]

References

1.3975

589

Svetlakov; Nikitin; Nikolaeva; Russian Journal of Organic Chemistry; vol. 43; nb. 5; (2007); p. 771 - 772, View in Reaxys

1.3975

589

19.99

Kirbaslar, S. Ismail; Sahin, Selin; Bilgin, Mehmet; Journal of Chemical Thermodynamics; vol. 39; nb. 2; (2007); p. 284 - 290, View in Reaxys

1.39599

589

Granados, Karla; Gracia-Fadrique, Jesus; Amigo, Alfredo; Bravo, Ramon; Journal of Chemical and Engineering Data; vol. 51; nb. 4; (2006); p. 1356 - 1360, View in Reaxys

1.3975

589

25.04

Kirbaslar, S. Ismail; Journal of Chemical Thermodynamics; vol. 38; nb. 6; (2006); p. 696 - 700, View in Reaxys

1.3982

589

19.99

Bilgin, Mehmet; Journal of Chemical Thermodynamics; vol. 38; nb. 12; (2006); p. 1634 - 1639, View in Reaxys

1.3978

589

Clifford, Scott L.; Ramjugernath, Deresh; Raal, J. David; Journal of Chemical and Engineering Data; vol. 49; nb. 5; (2004); p. 1189 1192, View in Reaxys

1.3962

589

Domonkos; Liszi; Zeitschrift fur Physikalische Chemie; vol. 214; nb. 1; (2000); p. 55 - 64, View in Reaxys

1.3955

589

Letcher; Redhi; Journal of Chemical and Engineering Data; vol. 45; nb. 1; (2000); p. 57 - 60, View in Reaxys

1.3916

589

Govindarajan; Sabarathinam; Journal of Chemical and Engineering Data; vol. 42; nb. 2; (1997); p. 402 - 408, View in Reaxys

1.3895 - 1.3978

589

20 - 50

Bernardo-Gil, Gabriela; Esquivel, Mercedes; Ribeiro, Albertina; Journal of Chemical & Engineering Data; vol. 35; nb. 2; (1990); p. 202 - 204, View in Reaxys

1.4026

589

Costisella, Burkhard; Gross, Hans; Tetrahedron; vol. 38; nb. 1; (1982); p. 139 - 145, View in Reaxys

1.399

589

Wollmann; Skaletzki; Schaaf; Die Pharmazie; vol. 29; nb. 10-11; (1974); p. 708 - 711, View in Reaxys; Bolotov,B.A. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 40; nb. 4; (1970); p. 823 - 827,802 - 806, View in Reaxys; Vereshchagin,L.I. et al.; Zhurnal Organicheskoi Khimii; vol. 11; nb. 2; (1975); p. 292 - 295,285 - 287, View in Reaxys; Vereshchagin,L.I. et al.; Zhurnal Organicheskoi Khimii; vol. 12; (1976); p. 1165 - 1169,1174 - 1178, View in Reaxys

1.39581

589

Dreisbach; Advances in Chemistry Series; p. 439, View in Reaxys; Radwan; Hanna; Journal of Chemical and Engineering Data; vol. 21; (1976); p. 285,286,287,288, View in Reaxys

1.398

589

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys; Radecki; Kaczmarek; Journal of Chemical and Engineering Data; vol. 20; (1975); p. 378,379,380, View in Reaxys

1.3984

589

Barton; Hsu; Journal of Chemical and Engineering Data; vol. 16; (1971); p. 93,94, View in Reaxys

1.3993

589

Shaw; Knutson; Journal of Organic Chemistry; vol. 36; (1971); p. 1151, View in Reaxys

28/428

2017-08-01 04:43:04

1.3979

589

Seinalow; Magerramowa; Azerbaidzhanskii Khimicheskii Zhurnal; vol. 2; (1965); p. 34,35; Chem.Abstr.; vol. 63; nb. 13131; (1965), View in Reaxys; Seinalew; Aliew; Azerbaidzhanskii Khimicheskii Zhurnal; vol. 1; (1964); p. 89,93; Chem.Abstr.; vol. 63; nb. 1711; (1965), View in Reaxys; Levitanaite et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 43; (1970); p. 115,107, View in Reaxys

1.3991

589

Chumachenko,T.K. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 40; nb. 4; (1970); p. 846 - 854,826 - 832, View in Reaxys

1.3988

589

Hukao; Nippon Kagaku Zasshi; vol. 88; (1967); p. 1044,1048, View in Reaxys

1.3968

589

Kachniaschwili et al.; Zhurnal Organicheskoi Khimii; vol. 2; (1966); p. 62,59, View in Reaxys

1.401

589

Goryaev et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 38; (1965); p. 2622,2563, View in Reaxys

1.4

589

Babel; Proskuryakov; J. Appl. Chem. USSR (Engl. Transl.); vol. 38; (1965); p. 1085,1064,1067, View in Reaxys

1.39551

589

Ismailow; Chimenko; Ukrainskii Khimicheskii Zhurnal (Russian Edition); vol. 30; (1964); p. 1266,1267, View in Reaxys

1.4072

589

Chiang; Li; Huaxue Xuebao; vol. 28; (1962); p. 379; Chem.Abstr.; vol. 59; nb. 12636; (1963), View in Reaxys

1.3992

589

Schelesnjak; Zhurnal Fizicheskoi Khimii; vol. 35; (1961); p. 322; engl. Ausgabe; p. 155, View in Reaxys

1.3958

589

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

1.3955

656.3

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

1.3977

589

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

1.4026

486.1

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

1.4061

434

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

1.39775

667.8

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys

1.39803

656.3

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys

1.4003

587.6

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys

1.40425

492.1

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys

1.4051

486.1

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys

1.40814

447

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys

1.40963

434

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys

1.3947

589

Ipatjew; Rasuwajew; Chemische Berichte; vol. 61; (1928); p. 636; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 60; (1928); p. 911, View in Reaxys

1.3756

656.3

Waterman; Bertram; Recueil des Travaux Chimiques des Pays-Bas; vol. 46; (1927); p. 701, View in Reaxys

1.3775

589

Waterman; Bertram; Recueil des Travaux Chimiques des Pays-Bas; vol. 46; (1927); p. 701, View in Reaxys

29/428

2017-08-01 04:43:04

1.3822

486.1

Waterman; Bertram; Recueil des Travaux Chimiques des Pays-Bas; vol. 46; (1927); p. 701, View in Reaxys

1.3859

434

Waterman; Bertram; Recueil des Travaux Chimiques des Pays-Bas; vol. 46; (1927); p. 701, View in Reaxys

1.399

589

Whitby; Journal of the Chemical Society; (1926); p. 1460, View in Reaxys

1.3983

589

Tromp; Recueil des Travaux Chimiques des Pays-Bas; vol. 41; (1922); p. 297, View in Reaxys

1.4004

589

Tromp; Recueil des Travaux Chimiques des Pays-Bas; vol. 41; (1922); p. 297, View in Reaxys

1.39582

656.3

20.3

Falk; Journal of the American Chemical Society; vol. 31; (1909); p. 91,92, View in Reaxys

1.39777

589

20.3

Falk; Journal of the American Chemical Society; vol. 31; (1909); p. 91,92, View in Reaxys

1.40271

486.1

20.3

Falk; Journal of the American Chemical Society; vol. 31; (1909); p. 91,92, View in Reaxys

1.40685

430.8

20.3

Falk; Journal of the American Chemical Society; vol. 31; (1909); p. 91,92, View in Reaxys

1.39906

589

Scheij; Recueil des Travaux Chimiques des Pays-Bas; vol. 18; (1899); p. 193, View in Reaxys

1.39811

656.3

19.1

Eijkman; Recueil des Travaux Chimiques des Pays-Bas; vol. 12; (1893); p. 181; Recueil des Travaux Chimiques des Pays-Bas; vol. 14; (1895); p. 188, View in Reaxys

1.40512

486.1

19.1

Eijkman; Recueil des Travaux Chimiques des Pays-Bas; vol. 12; (1893); p. 181; Recueil des Travaux Chimiques des Pays-Bas; vol. 14; (1895); p. 188, View in Reaxys

1.39578

656.3

Bruehl; Justus Liebigs Annalen der Chemie; vol. 203; (1880); p. 24, View in Reaxys

1.39789

589

Bruehl; Justus Liebigs Annalen der Chemie; vol. 203; (1880); p. 24, View in Reaxys

1.40691

434

Bruehl; Justus Liebigs Annalen der Chemie; vol. 203; (1880); p. 24, View in Reaxys

1.39554

656.3

Landolt; Ann.d.Physik; vol. 117; (1862); p. 382, View in Reaxys

1.40246

486.1

Landolt; Ann.d.Physik; vol. 117; (1862); p. 382, View in Reaxys

1.40649

434

Landolt; Ann.d.Physik; vol. 117; (1862); p. 382, View in Reaxys

1.39796

589

Dreisbach; Advances in Chemistry Series; p. 439, View in Reaxys

Density (83) 1 of 83

Density [g·cm-3]

0.93791

Measurement Temperature [°C]

39.99

Bahadur; Deenadayalu; Naidoo; Ramjugernath; Journal of Solution Chemistry; vol. 43; nb. 4; (2014); p. 787 803, View in Reaxys 2 of 83

Density [g·cm-3]

0.94288

Measurement Temperature [°C]

34.99

Bahadur; Deenadayalu; Naidoo; Ramjugernath; Journal of Solution Chemistry; vol. 43; nb. 4; (2014); p. 787 803, View in Reaxys 3 of 83

Density [g·cm-3]

0.94784

Measurement Temperature [°C]

29.99

Bahadur; Deenadayalu; Naidoo; Ramjugernath; Journal of Solution Chemistry; vol. 43; nb. 4; (2014); p. 787 803, View in Reaxys

30/428

2017-08-01 04:43:04

4 of 83

Density [g·cm-3]

0.95282

Measurement Temperature [°C]

24.99

Bahadur; Deenadayalu; Naidoo; Ramjugernath; Journal of Solution Chemistry; vol. 43; nb. 4; (2014); p. 787 803, View in Reaxys 5 of 83

Density [g·cm-3]

0.95778

Measurement Temperature [°C]

19.99

Bahadur; Deenadayalu; Naidoo; Ramjugernath; Journal of Solution Chemistry; vol. 43; nb. 4; (2014); p. 787 803, View in Reaxys 6 of 83

Density [g·cm-3]

0.93805

Measurement Temperature [°C]

39.99

Comment (Density)

Liquid

Bahadur; Singh; Deenadayalu; Naidoo; Ramjugernath; Thermochimica Acta; vol. 590; (2014); p. 151 - 159, View in Reaxys 7 of 83

Density [g·cm-3]

0.94292

Measurement Temperature [°C]

34.99

Comment (Density)

Liquid

Bahadur; Singh; Deenadayalu; Naidoo; Ramjugernath; Thermochimica Acta; vol. 590; (2014); p. 151 - 159, View in Reaxys 8 of 83

Density [g·cm-3]

0.94794

Measurement Temperature [°C]

29.99

Comment (Density)

Liquid

Bahadur; Singh; Deenadayalu; Naidoo; Ramjugernath; Thermochimica Acta; vol. 590; (2014); p. 151 - 159, View in Reaxys 9 of 83

Density [g·cm-3]

0.95281

Measurement Temperature [°C]

24.99

Comment (Density)

Liquid

Bahadur; Singh; Deenadayalu; Naidoo; Ramjugernath; Thermochimica Acta; vol. 590; (2014); p. 151 - 159, View in Reaxys 10 of 83

Density [g·cm-3]

0.95778

Measurement Temperature [°C]

19.99

Comment (Density)

Liquid

Bahadur; Singh; Deenadayalu; Naidoo; Ramjugernath; Thermochimica Acta; vol. 590; (2014); p. 151 - 159, View in Reaxys 11 of 83

Density [g·cm-3]

9.335E-06

Measurement Temperature [°C]

44.99

Comment (Density)

Liquid

Ahluwalia; Gupta, Ritu; Vashisht; Wanchoo; Journal of Solution Chemistry; vol. 42; nb. 5; (2013); p. 945 - 966, View in Reaxys 12 of 83

Density [g·cm-3]

9.434E-06

Measurement Temperature [°C]

34.99

31/428

2017-08-01 04:43:04

Comment (Density)

Liquid

Ahluwalia; Gupta, Ritu; Vashisht; Wanchoo; Journal of Solution Chemistry; vol. 42; nb. 5; (2013); p. 945 - 966, View in Reaxys 13 of 83

Density [g·cm-3]

9.533E-07

Measurement Temperature [°C]

24.99

Comment (Density)

Liquid

Ahluwalia; Gupta, Ritu; Vashisht; Wanchoo; Journal of Solution Chemistry; vol. 42; nb. 5; (2013); p. 945 - 966, View in Reaxys 14 of 83

Density [g·cm-3]

0.957608

Measurement Temperature [°C]

19.99

Suarez, Felipe; Romero, Carmen M.; Journal of Chemical and Engineering Data; vol. 56; nb. 5; (2011); p. 1778 1786, View in Reaxys 15 of 83

Density [g·cm-3]

0.952769

Measurement Temperature [°C]

24.99

Suarez, Felipe; Romero, Carmen M.; Journal of Chemical and Engineering Data; vol. 56; nb. 5; (2011); p. 1778 1786, View in Reaxys 16 of 83

Density [g·cm-3]

0.947942

Measurement Temperature [°C]

29.99

Suarez, Felipe; Romero, Carmen M.; Journal of Chemical and Engineering Data; vol. 56; nb. 5; (2011); p. 1778 1786, View in Reaxys 17 of 83

Density [g·cm-3]

0.942908

Measurement Temperature [°C]

34.99

Suarez, Felipe; Romero, Carmen M.; Journal of Chemical and Engineering Data; vol. 56; nb. 5; (2011); p. 1778 1786, View in Reaxys 18 of 83

Density [g·cm-3]

0.9528

Measurement Temperature [°C]

19.99

Kirbaslar, S. Ismail; Sahin, Selin; Bilgin, Mehmet; Journal of Chemical Thermodynamics; vol. 39; nb. 2; (2007); p. 284 - 290, View in Reaxys 19 of 83

Density [g·cm-3]

0.9528

Measurement Temperature [°C]

Merry; Turner; Journal of the Chemical Society; vol. 105; (1914); p. 758, View in Reaxys; Roy, Mahendra Nath; Sinha, Biswajit; Dakua, Vikas Kumar; Journal of Chemical and Engineering Data; vol. 51; nb. 2; (2006); p. 590 594, View in Reaxys 20 of 83

Density [g·cm-3]

0.95317

Measurement Temperature [°C]

Granados, Karla; Gracia-Fadrique, Jesus; Amigo, Alfredo; Bravo, Ramon; Journal of Chemical and Engineering Data; vol. 51; nb. 4; (2006); p. 1356 - 1360, View in Reaxys 21 of 83

Density [g·cm-3]

0.9523

Measurement Temperature [°C]

Bilgin, Mehmet; Ismail Kirbaslar; Oezean, Oender; Dramur, Umur; Journal of Chemical and Engineering Data; vol. 51; nb. 5; (2006); p. 1546 - 1550, View in Reaxys

32/428

2017-08-01 04:43:04

22 of 83

Density [g·cm-3]

0.9528

Measurement Temperature [°C]

25.04

Kirbaslar, S. Ismail; Journal of Chemical Thermodynamics; vol. 38; nb. 6; (2006); p. 696 - 700, View in Reaxys 23 of 83

Density [g·cm-3]

0.9576

Measurement Temperature [°C]

19.99

Bilgin, Mehmet; Journal of Chemical Thermodynamics; vol. 38; nb. 12; (2006); p. 1634 - 1639, View in Reaxys 24 of 83

Density [g·cm-3]

0.9311 - 0.962

Measurement Temperature [°C]

20 - 50

Sabolova, Erika; Schlosser, Stefan; Martak, Jan; Journal of Chemical and Engineering Data; vol. 46; nb. 3; (2001); p. 735 - 745, View in Reaxys 25 of 83

Density [g·cm-3]

0.953244

Measurement Temperature [°C]

Domonkos; Liszi; Zeitschrift fur Physikalische Chemie; vol. 214; nb. 1; (2000); p. 55 - 64, View in Reaxys 26 of 83

Density [g·cm-3]

0.9418

Measurement Temperature [°C]

Govindarajan; Sabarathinam; Journal of Chemical and Engineering Data; vol. 42; nb. 2; (1997); p. 402 - 408, View in Reaxys 27 of 83

Density [g·cm-3]

0.9279 - 0.9576

Measurement Temperature [°C]

20 - 50

Vong; Tsai; Journal of Chemical and Engineering Data; vol. 42; nb. 6; (1997); p. 1116 - 1120, View in Reaxys 28 of 83

Density [g·cm-3]

0.9524 - 0.9782

Measurement Temperature [°C]

20 - 50

Vong; Tsai; Journal of Chemical and Engineering Data; vol. 42; nb. 6; (1997); p. 1116 - 1120, View in Reaxys 29 of 83

Density [g·cm-3]

0.9393 - 0.9635

Measurement Temperature [°C]

20 - 50

Bernardo-Gil, Gabriela; Esquivel, Mercedes; Ribeiro, Albertina; Journal of Chemical & Engineering Data; vol. 35; nb. 2; (1990); p. 202 - 204, View in Reaxys 30 of 83

Density [g·cm-3]

0.9478

Measurement Temperature [°C]

Venkateswarlu; Raman; Journal of Chemical and Engineering Data; vol. 30; nb. 2; (1985); p. 180 - 181, View in Reaxys 31 of 83

Density [g·cm-3]

0.953

Measurement Temperature [°C]

Casanova, C.; Emmerich, Wilhelm; Grolier, J.-P. E.; Kehiaian, H. V.; Journal of Chemical Thermodynamics; vol. 13; nb. 3; (1981); p. 241 - 248, View in Reaxys 32 of 83

Density [g·cm-3]

0.95273

Measurement Temperature [°C]

Radwan; Hanna; Journal of Chemical and Engineering Data; vol. 21; (1976); p. 285,286,287,288, View in Reaxys

33/428

2017-08-01 04:43:04

33 of 83

Density [g·cm-3]

0.9587

Measurement Temperature [°C]

Radecki; Kaczmarek; Journal of Chemical and Engineering Data; vol. 20; (1975); p. 378,379,380, View in Reaxys 34 of 83

Density [g·cm-3]

0.959

Reference Temperature [°C]

Measurement Temperature [°C]

Wollmann; Skaletzki; Schaaf; Die Pharmazie; vol. 29; nb. 10-11; (1974); p. 708 - 711, View in Reaxys; Levitanaite et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 43; (1970); p. 115,107, View in Reaxys 35 of 83

Barton; Hsu; Journal of Chemical and Engineering Data; vol. 16; (1971); p. 93,94, View in Reaxys

36 of 83

Density [g·cm-3]

0.964

Reference Temperature [°C]

Measurement Temperature [°C]

Bolotov,B.A. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 40; nb. 4; (1970); p. 823 - 827,802 - 806, View in Reaxys; Lowry; Journal of the Chemical Society; vol. 105; (1914); p. 91, View in Reaxys 37 of 83

Density [g·cm-3]

0.9597

Reference Temperature [°C]

Measurement Temperature [°C]

Eremenko; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1970); p. 46,49; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1970); p. 50, View in Reaxys 38 of 83

Density [g·cm-3]

0.9645

Reference Temperature [°C]

Measurement Temperature [°C]

Chumachenko,T.K. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 40; nb. 4; (1970); p. 846 - 854,826 - 832, View in Reaxys 39 of 83

Density [g·cm-3]

0.9686

Reference Temperature [°C]

Measurement Temperature [°C]

Kachniaschwili et al.; Zhurnal Organicheskoi Khimii; vol. 2; (1966); p. 62,59, View in Reaxys 40 of 83

Density [g·cm-3]

0.9587

Reference Temperature [°C]

Measurement Temperature [°C]

Bruehl; Justus Liebigs Annalen der Chemie; vol. 203; (1880); p. 24, View in Reaxys; Seinalow; Magerramowa; Azerbaidzhanskii Khimicheskii Zhurnal; vol. 2; (1965); p. 34,35; Chem.Abstr.; vol. 63; nb. 13131; (1965), View in Reaxys; Seinalew; Aliew; Azerbaidzhanskii Khimicheskii Zhurnal; vol. 1; (1964); p. 89,93; Chem.Abstr.; vol. 63; nb. 1711; (1965), View in Reaxys 41 of 83

Density [g·cm-3]

0.9686

Measurement Temperature [°C]

34/428

2017-08-01 04:43:04

Paul et al.; Indian Journal of Chemistry; vol. 3; (1965); p. 239, View in Reaxys 42 of 83

Density [g·cm-3]

0.98189

Reference Temperature [°C]

Measurement Temperature [°C]

Ismailow; Chimenko; Ukrainskii Khimicheskii Zhurnal (Russian Edition); vol. 30; (1964); p. 1266,1267, View in Reaxys 43 of 83

Density [g·cm-3]

1.135

Comment (Density)

bei -43grad <berechnet>.

Strieter; U.S.Atomic Energy Comm.UCRL-8906; <1959>31, View in Reaxys; Strieter; Templeton; Acta Crystallographica; vol. 15; (1962); p. 1240,1243, View in Reaxys 44 of 83

Type (Density)

crystallographic

Strieter; Templeton; Acta Crystallographica; vol. 15; (1962); p. 1240,1243, View in Reaxys 45 of 83

Density [g·cm-3]

0.9549

Reference Temperature [°C]

Measurement Temperature [°C]

Chiang; Li; Huaxue Xuebao; vol. 28; (1962); p. 379; Chem.Abstr.; vol. 59; nb. 12636; (1963), View in Reaxys 46 of 83

Density [g·cm-3]

0.966

Reference Temperature [°C]

Measurement Temperature [°C]

Schelesnjak; Zhurnal Fizicheskoi Khimii; vol. 35; (1961); p. 322; engl. Ausgabe; p. 155, View in Reaxys 47 of 83

Density [g·cm-3]

0.9188

Reference Temperature [°C]

Measurement Temperature [°C]

Ssumarokowa; Nurmakowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 29,29; Chem.Abstr.; nb. 19134; (1960), View in Reaxys 48 of 83

Density [g·cm-3]

0.9378

Reference Temperature [°C]

Measurement Temperature [°C]

Ssumarokowa; Nurmakowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 29,29; Chem.Abstr.; nb. 19134; (1960), View in Reaxys 49 of 83

Density [g·cm-3]

0.9574

Reference Temperature [°C]

Measurement Temperature [°C]

Ssumarokowa; Nurmakowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 29,29; Chem.Abstr.; nb. 19134; (1960), View in Reaxys 50 of 83

Density [g·cm-3]

0.9767 - 0.6911

Measurement Temperature [°C]

0 - 260

35/428

2017-08-01 04:43:04

Costello; Bowden; Recueil des Travaux Chimiques des Pays-Bas; vol. 77; (1958); p. 803,808, View in Reaxys 51 of 83

Density [g·cm-3]

0.964

Measurement Temperature [°C]

Kotisek; Marek; Chemicky Prumysl; vol. 5; (1955); p. 330,331, 332; Chem.Abstr.; nb. 6239; (1960), View in Reaxys 52 of 83

Density [g·cm-3]

0.9577

Reference Temperature [°C]

Measurement Temperature [°C]

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys 53 of 83

Density [g·cm-3]

0.9527

Reference Temperature [°C]

Measurement Temperature [°C]

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys 54 of 83

Density [g·cm-3]

0.9563

Reference Temperature [°C]

Measurement Temperature [°C]

Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys 55 of 83

Density [g·cm-3]

0.9373

Reference Temperature [°C]

Measurement Temperature [°C]

41.2

Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys 56 of 83

Density [g·cm-3]

0.9187

Reference Temperature [°C]

Measurement Temperature [°C]

Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys 57 of 83

Density [g·cm-3]

0.8938

Reference Temperature [°C]

Measurement Temperature [°C]

86.8

Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys 58 of 83

Density [g·cm-3]

1.0875

Measurement Temperature [°C]

-12

Rozental; Bulletin des Societes Chimiques Belges; vol. 45; (1936); p. 585,600, View in Reaxys 59 of 83

Density [g·cm-3]

0.961

Measurement Temperature [°C]

13.5 - 16

36/428

2017-08-01 04:43:04

Comment (Density)

ref. temp. 4 Deg C

Kosakewitsch, P. P.; Kosakewitsch, N. S.; Z. phys. Ch.; vol. 166; (1933); p. 113 - 135, View in Reaxys; vol. Ca: MVol.B2; 112, page 531 - 533 ; (from Gmelin), View in Reaxys 60 of 83

Density [g·cm-3]

0.97762

Reference Temperature [°C]

Measurement Temperature [°C]

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys 61 of 83

Density [g·cm-3]

0.96286

Reference Temperature [°C]

Measurement Temperature [°C]

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys 62 of 83

Density [g·cm-3]

0.94797

Reference Temperature [°C]

Measurement Temperature [°C]

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys 63 of 83

Density [g·cm-3]

1.146

Measurement Temperature [°C]

-79

Biltz; Fischer; Wuennenberg; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 151; (1930); p. 18, View in Reaxys 64 of 83

Density [g·cm-3]

1.194

Measurement Temperature [°C]

-183

Biltz; Fischer; Wuennenberg; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 151; (1930); p. 18, View in Reaxys 65 of 83

Density [g·cm-3]

0.9784

Reference Temperature [°C]

Measurement Temperature [°C]

Grindley; Bury; Journal of the Chemical Society; (1929); p. 682, View in Reaxys; Grindley; Journal of the Chemical Society; (1928); p. 3297, View in Reaxys 66 of 83

Density [g·cm-3]

0.9664

Reference Temperature [°C]

Measurement Temperature [°C]

Grindley; Bury; Journal of the Chemical Society; (1929); p. 682, View in Reaxys 67 of 83

Density [g·cm-3]

0.9605

Reference Temperature [°C]

37/428

2017-08-01 04:43:04

Measurement Temperature [°C]

Grindley; Bury; Journal of the Chemical Society; (1929); p. 682, View in Reaxys 68 of 83

Density [g·cm-3]

0.9535

Reference Temperature [°C]

Measurement Temperature [°C]

Grindley; Bury; Journal of the Chemical Society; (1929); p. 682, View in Reaxys 69 of 83

Density [g·cm-3]

0.9437

Reference Temperature [°C]

Measurement Temperature [°C]

34.9

Grindley; Bury; Journal of the Chemical Society; (1929); p. 682, View in Reaxys 70 of 83

Density [g·cm-3]

0.8838 - 0.9792

Reference Temperature [°C]

Measurement Temperature [°C]

0.1 - 91.7

Hunten; Maass; Journal of the American Chemical Society; vol. 51; (1929); p. 159, View in Reaxys 71 of 83

Density [g·cm-3]

0.9573

Reference Temperature [°C]

Measurement Temperature [°C]

Ipatjew; Rasuwajew; Chemische Berichte; vol. 61; (1928); p. 636; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 60; (1928); p. 911, View in Reaxys 72 of 83

Density [g·cm-3]

0.9583

Reference Temperature [°C]

Measurement Temperature [°C]

Rasuwajew; Chemische Berichte; vol. 60; (1927); p. 1979; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 59; (1927); p. 1075, View in Reaxys 73 of 83

Density [g·cm-3]

0.938

Measurement Temperature [°C]

Merry; Turner; Journal of the Chemical Society; vol. 105; (1914); p. 758, View in Reaxys 74 of 83

Density [g·cm-3]

0.96

Reference Temperature [°C]

Measurement Temperature [°C]

18.7

Dobrosserdow; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 43; (1911); p. 125; Chem. Zentralbl.; vol. 82; nb. I; (1911); p. 955, View in Reaxys 75 of 83

Density [g·cm-3]

0.9113

Reference Temperature [°C]

38/428

2017-08-01 04:43:04

Measurement Temperature [°C]

67.4

Falk; Journal of the American Chemical Society; vol. 31; (1909); p. 91,92, View in Reaxys 76 of 83

Density [g·cm-3]

0.9534

Reference Temperature [°C]

Measurement Temperature [°C]

24.7

Falk; Journal of the American Chemical Society; vol. 31; (1909); p. 91,92, View in Reaxys 77 of 83

Density [g·cm-3]

1.2016

Reference Temperature [°C]

100

Measurement Temperature [°C]

100

Thoerner; Chem. Zentralbl.; vol. 79; nb. I; (1908); p. 2002, View in Reaxys 78 of 83

Density [g·cm-3]

0.8983

Reference Temperature [°C]

Measurement Temperature [°C]

80.9

Eijkman; Recueil des Travaux Chimiques des Pays-Bas; vol. 12; (1893); p. 181; Recueil des Travaux Chimiques des Pays-Bas; vol. 14; (1895); p. 188, View in Reaxys 79 of 83

Density [g·cm-3]

0.9599

Reference Temperature [°C]

Measurement Temperature [°C]

19.1

Eijkman; Recueil des Travaux Chimiques des Pays-Bas; vol. 12; (1893); p. 181; Recueil des Travaux Chimiques des Pays-Bas; vol. 14; (1895); p. 188, View in Reaxys 80 of 83

Density [g·cm-3]

0.9746

Measurement Temperature [°C]

Zander; Justus Liebigs Annalen der Chemie; vol. 224; (1884); p. 81, View in Reaxys 81 of 83

Density [g·cm-3]

0.8141

Reference Temperature [°C]

Measurement Temperature [°C]

161.5

Schiff,R.; Justus Liebigs Annalen der Chemie; vol. 220; (1883); p. 288, View in Reaxys 82 of 83

Density [g·cm-3]

0.95273

Reference Temperature [°C]

Measurement Temperature [°C]

Dreisbach; Advances in Chemistry Series; p. 439, View in Reaxys 83 of 83

Density [g·cm-3]

0.95767

Measurement Temperature [°C]

Dreisbach; Advances in Chemistry Series; p. 439, View in Reaxys

39/428

2017-08-01 04:43:04

Adsorption (MCS) (91) 1 of 91

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

carbon from oil-palm shell, impregnated with 60percent KOH

Ruiz, Hector; Zambtrano, Monica; Giraldo, Liliana; Sierra, Rocio; Moreno-Pirajan, Juan Carlos; Oriental Journal of Chemistry; vol. 31; nb. 2; (2015); p. 753 - 762, View in Reaxys 2 of 91

Description (Adsorption (MCS))

Desorption

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

carbon from oil-palm shell, impregnated with 60percent KOH

Ruiz, Hector; Zambtrano, Monica; Giraldo, Liliana; Sierra, Rocio; Moreno-Pirajan, Juan Carlos; Oriental Journal of Chemistry; vol. 31; nb. 2; (2015); p. 753 - 762, View in Reaxys 3 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

acidic aq. solution

Temperature (Adsorption (MCS)) [°C]

Pressure (Adsorption (MCS)) [Torr]

759.826

Location

Paragraph 0067

Partner (Adsorption (MCS))

Amberlite® XAD-4

Patent; SOLVAY SA; Dournel, Pierre; EP2602240; (2013); (A1) English, View in Reaxys 4 of 91

Description (Adsorption (MCS))

Adsorption isotherm

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

MCM-41 type amine-functionalized mesoporous silica

Kim, Sang-Hyoun; Huang, Yulin; Sawatdeenarunat, Chayanon; Sung, Shihwu; Lin, Victor S.-Y.; Journal of Materials Chemistry; vol. 21; nb. 32; (2011); p. 12103 - 12109, View in Reaxys 5 of 91

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

quartz sand

Arp, Hans Peter H.; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Toxicology and Chemistry; vol. 25; nb. 1; (2006); p. 45 - 51, View in Reaxys 6 of 91

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

SiO2

Da Graca Nascimento, Maria; Zanotto, Sandra Patricia; Scremin, Marivania; Rezende, Marcos Caroli; Synthetic Communications; vol. 26; nb. 14; (1996); p. 2715 - 2721, View in Reaxys 7 of 91

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

40/428

2017-08-01 04:43:04

Solvent (Adsorption (MCS))

H2O

Temperature (Adsorption (MCS)) [°C]

19 - 21

Partner (Adsorption (MCS))

hydroxylated silica

Basiuk, V.A.; Gromovoy, T.Yu.; Khil'chevskaya, E.G.; Polish Journal of Chemistry; vol. 69; nb. 1; (1995); p. 127 131, View in Reaxys 8 of 91

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

poly(acrylate)-coated fiber

Pan, Lin; Adams, Marc; Pawliszyn, Janusz; Analytical Chemistry; vol. 67; nb. 23; (1995); p. 4396 - 4403, View in Reaxys 9 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

phenol; porolas VP-3

Podlesnyuk, V. V.; Fridman, L. E.; Fesenko, E. A.; Russian Journal of Physical Chemistry; vol. 68; nb. 8; (1994); p. 1319 - 1321; Zhurnal Fizicheskoi Khimii; vol. 68; nb. 8; (1994); p. 1452 - 1454, View in Reaxys 10 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

porolas VP-3

Description (Adsorption (MCS))

Adsorption isotherm

Solvent (Adsorption (MCS))

decane

Partner (Adsorption (MCS))

KSK-2 silica gel

Okisheva, N. A.; Rakhlevskaya, M. N.; Rodzivilova, I. S.; Russian Journal of Physical Chemistry; vol. 68; nb. 10; (1994); p. 1739 - 1741; Zhurnal Fizicheskoi Khimii; vol. 68; nb. 10; (1994); p. 1912 - 1914, View in Reaxys 12 of 91

Description (Adsorption (MCS))

Chemisorption

Partner (Adsorption (MCS))

Smith, Earl L.; Porter, Marc D.; Journal of Physical Chemistry; vol. 97; nb. 30; (1993); p. 8032 - 8038, View in Reaxys 13 of 91

Description (Adsorption (MCS))

Adsorption isotherm

Solvent (Adsorption (MCS))

benzene

Partner (Adsorption (MCS))

CaX zeolite

Rodzivilova, I. S.; Rakhlevskaya, M. N.; Ryabukhova, T. O.; Petrova, E. N.; Russian Journal of Physical Chemistry; vol. 66; nb. 2; (1992); p. 297 - 298; Zhurnal Fizicheskoi Khimii; vol. 66; (1992); p. 564 - 566, View in Reaxys

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14 of 91

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

nitromethane

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 15 of 91

Description (Adsorption (MCS))

Adsorption isotherm

Solvent (Adsorption (MCS))

heptane

Temperature (Adsorption (MCS)) [°C]

39.9

Partner (Adsorption (MCS))

η-Al2O3

Stradella; Venturello; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 87; nb. 1; (1983); p. 11 - 17, View in Reaxys 16 of 91

Description (Adsorption (MCS))

Adsorption isotherm

Solvent (Adsorption (MCS))

heptane

Temperature (Adsorption (MCS)) [°C]

39.9

Partner (Adsorption (MCS))

α-Al2O3

Stradella; Venturello; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 87; nb. 1; (1983); p. 11 - 17, View in Reaxys 17 of 91

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Partner (Adsorption (MCS))

decane; zeolites

Rakhlevskaya, M. N.; Rodzivilova, I. S.; Russian Journal of Physical Chemistry; vol. 57; nb. 6; (1983); p. 920 921; Zhurnal Fizicheskoi Khimii; vol. 57; (1983); p. 1524 - 1525, View in Reaxys 18 of 91

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Partner (Adsorption (MCS))

decane; 1-Decanol; zeolites

Description (Adsorption (MCS))

Chemisorption

Partner (Adsorption (MCS))

Amberlite-IR-120

Adhikary, S. K.; Pochhali, L.; Ray, K. C.; Journal of the Indian Chemical Society; vol. 57; nb. 12; (1980); p. 1200 1203, View in Reaxys 20 of 91

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Partner (Adsorption (MCS))

H2O, air

Vilallonga; Phillips; Journal of Pharmaceutical Sciences; vol. 69; nb. 1; (1980); p. 65 - 71, View in Reaxys 21 of 91

Description (Adsorption (MCS))

Adsorption

Cornford et al.; Transactions of the Faraday Society; vol. 58; (1962); p. 74,78, View in Reaxys; Welch et al.; Journal of Physical Chemistry; vol. 65; (1965); p. 705, View in Reaxys; Slinyakova; Budkevich; Sov. Prog. Chem.

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(Engl. Transl.); vol. 33; nb. 2; (1967); p. 157,35, View in Reaxys; Tsuruizumi; Bulletin of the Chemical Society of Japan; vol. 34; (1961); p. 1457,1463, 1464, View in Reaxys; England; Berg; AIChE Journal; vol. 17; (1971); p. 313,319, View in Reaxys; Wang et al.; Journal of Chemical and Engineering Data; vol. 24; (1979); p. 345,346,347, View in Reaxys; Zdrazil; Journal of Catalysis; vol. 58; (1979); p. 436, View in Reaxys; Shakkak et al.; Moscow University Chemistry Bulletin (English Translation); vol. 27; nb. 4; (1971); p. 41; ; p. 424, View in Reaxys; Loutfy; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 38; (1972); p. 283,284, View in Reaxys; Hukao; Nippon Kagaku Zasshi; vol. 88; (1967); p. 1044,1048, View in Reaxys; Abe et al.; Bulletin of the Chemical Society of Japan; vol. 52; (1979); p. 1899,1901, 1903, View in Reaxys; Gryazev et al.; Russian Journal of Physical Chemistry; vol. 50; (1976); p. 1762; ; p. 2960, View in Reaxys; Semenkina et al.; Russian Journal of Physical Chemistry; vol. 51; (1977); p. 699; ; p. 1194, View in Reaxys; Kaganovich et al.; Doklady Physical Chemistry; vol. 154-156; (1964); p. 361; Doklady Akademii Nauk SSSR; vol. 155; (1964); p. 893, View in Reaxys; Drozhalina et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 48; (1975); p. 1264,1320, View in Reaxys; Brown et al.; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 75; (1979); p. 261,263, 266, View in Reaxys 22 of 91

Description (Adsorption (MCS))

Adsorption isotherm

Laitinen; Analytical Chemistry; vol. 33; (1961); p. 1458,1462, View in Reaxys; Litkovets; Zeliznyi; Sov. Prog. Chem. (Engl. Transl.); vol. 35; nb. 8; (1969); p. 809,24, View in Reaxys; Abramzon et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 46; (1976); p. 1609,1566,1567, View in Reaxys; Abe et al.; Bulletin of the Chemical Society of Japan; vol. 52; (1979); p. 1899,1901, 1903, View in Reaxys; Afzal; Naseer; Pakistan Journal of Scientific and Industrial Research; vol. 15; (1972); p. 137, View in Reaxys 23 of 91

Description (Adsorption (MCS))

Enthalpy of adsorption

Dear et al.; Transactions of the Faraday Society; vol. 59; (1963); p. 713,717, View in Reaxys; Chattoraj; Journal of the Indian Chemical Society; vol. 56; (1979); p. 1065,1067, View in Reaxys 24 of 91

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

mercury

Lorenz; Moeckel; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 60; (1956); p. 507, View in Reaxys 25 of 91

Partner (Adsorption (MCS))

graphite

Kiselev, A. V.; Shikalova, I. V.; Zhurnal Fizicheskoi Khimii; vol. 30; (1956); p. 94 - 108 ; (from Gmelin), View in Reaxys 26 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

graphite

Fu; Hansen; Bartell; Journal of Physical Chemistry; vol. 52; (1948); p. 378, View in Reaxys 27 of 91

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

BaSO4

Kiselev, A. V.; Kiseleva, T. S.; Doklady Akademii Nauk SSSR; vol. 59; (1948); p. 925 - 928, View in Reaxys; vol. Ba: SVol.; 132, page 429 - 431 ; (from Gmelin), View in Reaxys 28 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

coal

Roychoudhury; Kolloid-Zeitschrift; vol. 57; (1931); p. 310, View in Reaxys; Landt; Knop; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 162; (1932); p. 336, View in Reaxys; Woehler; Wenzel; Kolloid-Zeitschrift; vol. 53; (1930); p. 274, View in Reaxys; Lemieux;

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Morrison; Canadian Journal of Research, Section B: Chemical Sciences; vol. 25; (1947); p. 442, View in Reaxys; Kisselew; Schtscherbakowa; Doklady Akademii Nauk SSSR; vol. 45; (1944); p. 257; Doklady Akademii Nauk SSSR; vol. 45; (1944); p. 243; Chem.Abstr.; (1945); p. 5150, View in Reaxys; Jermolenko; Gendelmann; Rabinowitsch; Kolloidnyi Zhurnal; vol. 3; (1937); p. 299; Chem. Zentralbl.; vol. 109; nb. I; (1938); p. 864, View in Reaxys; Linner; Gortner; Journal of Physical Chemistry; vol. 39; (1935); p. 40, View in Reaxys; King; Journal of the Chemical Society; (1934); p. 1978, View in Reaxys; Krczil; Kolloid-Zeitschrift; vol. 58; (1932); p. 72, View in Reaxys; Lepin; Zhurnal Obshchei Khimii; vol. 1; (1931); p. 390; Chem. Zentralbl.; vol. 103; nb. I; (1932); p. 1210, View in Reaxys; Bruns; Kolloid-Zeitschrift; vol. 54; (1931); p. 34, View in Reaxys; Angelescu; Soloviu; Bulet.Soc.Chim.Romania; vol. 19; (1937); p. 65; Chem. Zentralbl.; vol. 110; nb. I; (1939); p. 608, View in Reaxys; Dubinin; Sawerina; Zhurnal Fizicheskoi Khimii; vol. 4; (1933); p. 308; Chem. Zentralbl.; vol. 105; nb. II; (1934); p. 1105, View in Reaxys; Bruns; Zarubina; Kolloid-Zeitschrift; vol. 64; (1933); p. 284, View in Reaxys; Heymann; Boye; Kolloid-Zeitschrift; vol. 63; (1933); p. 159, View in Reaxys 29 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

CCl4

Partner (Adsorption (MCS))

silica gel

Rychlikow; Gapon; Zhurnal Fizicheskoi Khimii; vol. 20; (1946); p. 1029; Chem.Abstr.; (1947); p. 2298, View in Reaxys; Rychlikow; Chem.Abstr.; (1942); p. 6062, View in Reaxys 30 of 91

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

silica gel;

Bartell, F. E.; Fu, Y.; Colloid Symposium Annual; vol. 7; (1929); p. 135 - 139, View in Reaxys; Gapon, E. N.; Zhurnal Fizicheskoi Khimii; vol. 11; (1938); p. 651 - 653; C. I; (1939); p. 2956, View in Reaxys; Mehrotra, M. R.; Dhar, N. R.; Z. Anorg. Chem.; vol. 155; (1926); p. 298 - 302, View in Reaxys; Patrick, W. A.; Jones, D. C.; Journal of Physical Chemistry; vol. 29; (1925); p. 1 - 10, View in Reaxys; Rychlikov, G. P.; Gapon, E. N.; Zhurnal Fizicheskoi Khimii; vol. 20; (1946); p. 1029 - 1041; C. A.; (1947); p. 2298, View in Reaxys; Rychlikov, G. P.; Vses. Akad. sel'skoKhoz. Nauk Inst. Udobr. Tr. Leningr....; nb. 2; (1938); p. 357 - 374; C. II; (1940); p. 3598, View in Reaxys; vol. Si: MVol.B; 185, page 525 - 527 ; (from Gmelin), View in Reaxys 31 of 91

Description (Adsorption (MCS))

Adsorption

Comment (Adsorption (MCS))

aus verschiedenen organischen Loesungsmitteln und Loesungsmittel-Gemischen.

Partner (Adsorption (MCS))

coal

Ginzburg; Chem.Abstr.; (1943); p. 2243, View in Reaxys; Jermolenko; Lewina; Acta physicoch.U.R.S.S.; vol. 10; (1939); p. 453; Chem. Zentralbl.; vol. 110; nb. II; (1939); p. 3679, View in Reaxys 32 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

ethanol

Partner (Adsorption (MCS))

silica gel

Gyani; Ganguly; Journal of the Indian Chemical Society; vol. 20; (1943); p. 332; Chem.Abstr.; (1944); p. 3180, View in Reaxys 33 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

toluene

Partner (Adsorption (MCS))

glass powder

Akamatsu; Bulletin of the Chemical Society of Japan; vol. 17; (1942); p. 144, View in Reaxys 34 of 91

Description (Adsorption (MCS))

Adsorption

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Solvent (Adsorption (MCS))

benzene

Partner (Adsorption (MCS))

glass powder

Akamatsu; Bulletin of the Chemical Society of Japan; vol. 17; (1942); p. 144, View in Reaxys 35 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

silica gel

Posspelowa; Zhurnal Fizicheskoi Khimii; vol. 11; (1938); p. 99; Chem. Zentralbl.; vol. 109; nb. II; (1938); p. 276, View in Reaxys 36 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

petroleum ether

Partner (Adsorption (MCS))

silica gel

Posspelowa; Zhurnal Fizicheskoi Khimii; vol. 11; (1938); p. 99; Chem. Zentralbl.; vol. 109; nb. II; (1938); p. 276, View in Reaxys 37 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

quartz

Buzagh; Zimmermann; Kolloid-Zeitschrift; vol. 84; (1938); p. 17, View in Reaxys 38 of 91

Description (Adsorption (MCS))

Adsorption

Comment (Adsorption (MCS))

Adsorption des Dampfes.

Partner (Adsorption (MCS))

MnO2

Alexejewsski; Golbraich; Zhurnal Obshchei Khimii; vol. 4; (1934); p. 936,938, 940; Chem. Zentralbl.; vol. 106; nb. II; (1935); p. 3750, View in Reaxys 39 of 91

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

Comment (Adsorption (MCS))

Adsorption des Dampfes.

Partner (Adsorption (MCS))

activated sugar-coal

McBain; Sessions; Journal of the American Chemical Society; vol. 56; (1934); p. 3; J. Colloid Sci.; vol. 3; (1948); p. 216; Chem.Abstr.; (1948); p. 6198, View in Reaxys 40 of 91

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

120

Comment (Adsorption (MCS))

Adsorption des Dampfes.

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Partner (Adsorption (MCS))

activated sugar-coal

McBain; Sessions; Journal of the American Chemical Society; vol. 56; (1934); p. 3; J. Colloid Sci.; vol. 3; (1948); p. 216; Chem.Abstr.; (1948); p. 6198, View in Reaxys 41 of 91

Description (Adsorption (MCS))

Adsorption

Comment (Adsorption (MCS))

Adsorption des Dampfes.

Partner (Adsorption (MCS))

mercury

Bosworth; Transactions of the Faraday Society; vol. 28; (1932); p. 903; Chem. Zentralbl.; vol. 104; nb. I; (1933); p. 2072, View in Reaxys 42 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

aq. HCl

Partner (Adsorption (MCS))

coal

Landt; Knop; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 162; (1932); p. 336, View in Reaxys 43 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O; ethanol

Partner (Adsorption (MCS))

coal

Reif; von der Heide; Z.Unters.Lebensm.; vol. 64; (1932); p. 515, View in Reaxys 44 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

gold powder

Heymann; Boye; Kolloid-Zeitschrift; vol. 59; (1932); p. 154, View in Reaxys 45 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

benzene

Partner (Adsorption (MCS))

gold powder

Heymann; Boye; Kolloid-Zeitschrift; vol. 59; (1932); p. 154, View in Reaxys 46 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

ethanol

Partner (Adsorption (MCS))

gold powder

Heymann; Boye; Kolloid-Zeitschrift; vol. 59; (1932); p. 154, View in Reaxys 47 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

acetone

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Partner (Adsorption (MCS))

gold powder

Heymann; Boye; Kolloid-Zeitschrift; vol. 59; (1932); p. 154, View in Reaxys 48 of 91

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

125 - 190

Comment (Adsorption (MCS))

Adsorption des Dampfes.

Partner (Adsorption (MCS))

activated sugar-coal

McBain et al.; Journal of Physical Chemistry; vol. 34; (1930); p. 1441, View in Reaxys 49 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

zirconium hydroxide

Chakravarty; Sen; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 186; (1930); p. 360, View in Reaxys 50 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

platinum black

Platonow; Borgman; Ssalman; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 62; (1930); p. 1982; Chem. Zentralbl.; vol. 102; nb. II; (1931); p. 2438, View in Reaxys 51 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

diethyl ether

Partner (Adsorption (MCS))

platinum black

Platonow; Borgman; Ssalman; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 62; (1930); p. 1982; Chem. Zentralbl.; vol. 102; nb. II; (1931); p. 2438, View in Reaxys 52 of 91

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

ZrO2*xH2O

Chakravarty, S. N.; Sen, K. C.; Z. Anorg. Chem.; vol. 186; (1930); p. 357 - 364, View in Reaxys; vol. Zr: MVol.; 93, page 252 - 255 ; (from Gmelin), View in Reaxys 53 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Comment (Adsorption (MCS))

an verschiedene Adsorptionskohlen.

Sabalitschka; Pharm.Ztg.; vol. 74; p. 382; Chem. Zentralbl.; vol. 100; nb. I; (1929); p. 2288, View in Reaxys; Nekrassow; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 136; (1928); p. 22, View in Reaxys 54 of 91

Description (Adsorption (MCS))

Adsorption

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Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

silicic acid-gel

Bartell; Fu; Journal of Physical Chemistry; vol. 33; (1929); p. 680, View in Reaxys; Mehrotra; Dhar; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 155; (1926); p. 299, View in Reaxys 55 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

CCl4

Partner (Adsorption (MCS))

silicic acid-gel

Bartell; Fu; Journal of Physical Chemistry; vol. 33; (1929); p. 680, View in Reaxys 56 of 91

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

aqueous butyric acid

McBain; du Bois; Journal of the American Chemical Society; vol. 51; (1929); p. 3543, View in Reaxys 57 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

sugar-coal

Nekrassow; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 136; (1928); p. 380, View in Reaxys; Bartell; Miller; Journal of the American Chemical Society; vol. 45; (1923); p. 1109, View in Reaxys 58 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

coconut coal

Namasivayam; Quart.J.indian chem.Soc.; vol. 4; p. 452; Chem. Zentralbl.; vol. 99; nb. I; (1928); p. 662, View in Reaxys 59 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

ethanol

Partner (Adsorption (MCS))

charcoal

Griffin; Richardson; Robertson; Journal of the Chemical Society; (1928); p. 2708, View in Reaxys 60 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

ethanol

Comment (Adsorption (MCS))

an verschiedene Adsorptionskohlen.

Nekrassow; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 136; (1928); p. 22, View in Reaxys 61 of 91

Description (Adsorption (MCS))

Adsorption

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Solvent (Adsorption (MCS))

CHCl3

Comment (Adsorption (MCS))

an verschiedene Adsorptionskohlen.

Nekrassow; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 136; (1928); p. 22, View in Reaxys 62 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

CCl4

Comment (Adsorption (MCS))

an verschiedene Adsorptionskohlen.

Nekrassow; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 136; (1928); p. 22, View in Reaxys 63 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

CS2

Comment (Adsorption (MCS))

an verschiedene Adsorptionskohlen.

Nekrassow; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 136; (1928); p. 22, View in Reaxys 64 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

light petroleum

Comment (Adsorption (MCS))

an verschiedene Adsorptionskohlen.

Nekrassow; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 136; (1928); p. 22, View in Reaxys 65 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

methanol

Comment (Adsorption (MCS))

an verschiedene Adsorptionskohlen.

Nekrassow; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 136; (1928); p. 22, View in Reaxys 66 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

diethyl ether

Comment (Adsorption (MCS))

an verschiedene Adsorptionskohlen.

Nekrassow; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 136; (1928); p. 22, View in Reaxys 67 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

acetone

Comment (Adsorption (MCS))

an verschiedene Adsorptionskohlen.

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Nekrassow; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 136; (1928); p. 22, View in Reaxys 68 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

benzene

Comment (Adsorption (MCS))

an verschiedene Adsorptionskohlen.

Nekrassow; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 136; (1928); p. 22, View in Reaxys 69 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

toluene

Comment (Adsorption (MCS))

an verschiedene Adsorptionskohlen.

Nekrassow; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 136; (1928); p. 22, View in Reaxys 70 of 91

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

Comment (Adsorption (MCS))

Adsorption des Gemisches mit Glycerinbutyrat aus Loesungen mit Glycerin.

Partner (Adsorption (MCS))

charcoal

Przylecki; Giedroyc; Sym; Biochemical Journal; vol. 22; (1928); p. 824, View in Reaxys 71 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

viscose

Brass; Frei; Kolloid-Zeitschrift; vol. 45; p. 249; Chem. Zentralbl.; vol. 99; nb. II; (1928); p. 1037, View in Reaxys 72 of 91

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

water

Bury; Phil.Mag.; vol. <7>4; p. 981; Chem. Zentralbl.; vol. 99; nb. I; (1928); p. 1266, View in Reaxys 73 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

charcoal

Traube; Somogyi; Biochemische Zeitschrift; vol. 120; (1921); p. 98, View in Reaxys; Traube; Verh.dtsch.phys.Ges.; vol. 10; (1908); p. 901, View in Reaxys; Watson; Biochemical Journal; vol. 16; (1922); p. 617, View in Reaxys; Alexejewski; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 59; (1927); p. 1036; Chem. Zentralbl.; vol. 99; nb. I; (1928); p. 2916, View in Reaxys; Freundlich; Birstein; Koll.Beih.; vol. 22; (1926); p. 96, View in Reaxys; Klein; Lotos; vol. 71; (1923); p. 286,292, View in Reaxys; Schilow; Nekrassow; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 130; (1927); p. 70; Zhurnal Russkago FizikoKhimicheskago Obshchestva; vol. 60; (1928); p. 110, View in Reaxys

50/428

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74 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Comment (Adsorption (MCS))

Adsorption aus Gemischen mit Crotonsaeure.

Partner (Adsorption (MCS))

charcoal

Alexejewski; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 59; (1927); p. 1036; Chem. Zentralbl.; vol. 99; nb. I; (1928); p. 2916, View in Reaxys 75 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

iron (III)-hydroxide

Sen; Journal of Physical Chemistry; vol. 31; (1927); p. 526, View in Reaxys 76 of 91

Description (Adsorption (MCS))

Adsorption

Comment (Adsorption (MCS))

von fluessiger Buttersaeure.

Partner (Adsorption (MCS))

platinum

Palmer; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 115; (1927); p. 229; Chem. Zentralbl.; vol. 98; nb. II; (1927); p. 1678, View in Reaxys 77 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

skin powder

Kubelka; Taussig; Koll.Beih.; vol. 22; p. 153,159; Chem. Zentralbl.; vol. 97; nb. II; (1926); p. 2138, View in Reaxys 78 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

toluene

Partner (Adsorption (MCS))

silicic acid-gel

Patrick; Jones; Journal of Physical Chemistry; vol. 29; (1925); p. 4, View in Reaxys 79 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

kerosene

Partner (Adsorption (MCS))

silicic acid-gel

Patrick; Jones; Journal of Physical Chemistry; vol. 29; (1925); p. 4, View in Reaxys 80 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

petroleum ether

Partner (Adsorption (MCS))

silicic acid-gel

51/428

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Patrick; Jones; Journal of Physical Chemistry; vol. 29; (1925); p. 4, View in Reaxys 81 of 91

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

Comment (Adsorption (MCS))

des Dampfes.

Partner (Adsorption (MCS))

charcoal

Alexejewski; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 55; (1924); p. 416; Chem. Zentralbl.; vol. 96; nb. II; (1925); p. 642, View in Reaxys 82 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

starch

Lasnitzki; Loeb; Biochemische Zeitschrift; vol. 146; (1924); p. 101,102, View in Reaxys 83 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

gelatine

Lasnitzki; Loeb; Biochemische Zeitschrift; vol. 146; (1924); p. 101,102, View in Reaxys 84 of 91

Description (Adsorption (MCS))

Adsorption

Comment (Adsorption (MCS))

an Kohle, Tonerde, Wolle.

Lachs; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 91; (1916); p. 160, View in Reaxys 85 of 91

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

coal

Freundlich; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 57; (1907); p. 433, View in Reaxys 86 of 91

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

H2O

Temperature (Adsorption (MCS)) [°C]

Partner (Adsorption (MCS))

siloxene

Kautsky; Blinoff; Ph.Ch.<A>; vol. 139; p. 509, View in Reaxys 87 of 91

Description (Adsorption (MCS))

Enthalpy of adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

silicic acid

52/428

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Rehbinder; Krajuschkina; Ph.Ch.<A>; vol. 142; p. 285, View in Reaxys 88 of 91

Description (Adsorption (MCS))

Enthalpy of adsorption

Solvent (Adsorption (MCS))

hexane

Partner (Adsorption (MCS))

silicic acid

Rehbinder; Krajuschkina; Ph.Ch.<A>; vol. 142; p. 285, View in Reaxys 89 of 91

Description (Adsorption (MCS))

Enthalpy of adsorption

Solvent (Adsorption (MCS))

H2O

Partner (Adsorption (MCS))

coal

Rehbinder; Krajuschkina; Ph.Ch.<A>; vol. 142; p. 285, View in Reaxys 90 of 91

Description (Adsorption (MCS))

Enthalpy of adsorption

Solvent (Adsorption (MCS))

hexane

Partner (Adsorption (MCS))

coal

Rehbinder; Krajuschkina; Ph.Ch.<A>; vol. 142; p. 285, View in Reaxys 91 of 91

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

graphite

vol. C: MVol.B2; 87, page 736 - 738 ; (from Gmelin), View in Reaxys Association (MCS) (63) 1 of 63

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

H2O

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

alpha cyclodextrin

Buschmann, Hans-Juergen; Schollmeyer, Eckhard; Journal of Solution Chemistry; vol. 34; nb. 6; (2005); p. 731 737, View in Reaxys 2 of 63

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

H2O

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

alpha cyclodextrin

Buschmann, Hans-Juergen; Schollmeyer, Eckhard; Journal of Solution Chemistry; vol. 34; nb. 6; (2005); p. 731 737, View in Reaxys 3 of 63

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

rccc-4,6,10,12,16,18,22,24-octahydroxy-2,8,14,20-tetra-n-undecylpyridine[4]arene

53/428

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

[2,2']bi[[1,3]dithiolylidene]-4-carboxylic acid (6-methyl-pyridin-2-yl)-amide

Boyd, Alan S.F.; Cooke, Graeme; Duclairoir, Florence M.A.; Rotello, Vincent M.; Tetrahedron Letters; vol. 44; nb. 2; (2003); p. 303 - 306, View in Reaxys 5 of 63

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

CH2Cl2

Partner (Association (MCS))

[2,2']bi[[1,3]dithiolylidene]-4-carboxylic acid (6-methyl-pyridin-2-yl)-amide

Boyd, Alan S.F.; Cooke, Graeme; Duclairoir, Florence M.A.; Rotello, Vincent M.; Tetrahedron Letters; vol. 44; nb. 2; (2003); p. 303 - 306, View in Reaxys 6 of 63

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

5 - 95

Pressure (Association (MCS)) [Torr]

2625.21

Comment (Association (MCS))

concentration dependence. Object(s) of Study: temperature dependence

Partner (Association (MCS))

H2O

McRae; Patterson; Origlia-Luster; Sorenson; Woolley; Journal of Chemical Thermodynamics; vol. 35; nb. 2; (2003); p. 301 - 329, View in Reaxys 7 of 63

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

acetic acid; propionic acid

Miyamoto, Shinji; Nakamura, Shinichi; Iwai, Yoshio; Arai, Yasuhiko; Journal of Chemical and Engineering Data; vol. 46; nb. 5; (2001); p. 1225 - 1230, View in Reaxys 8 of 63

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

propionic acid

Miyamoto, Shinji; Nakamura, Shinichi; Iwai, Yoshio; Arai, Yasuhiko; Journal of Chemical and Engineering Data; vol. 46; nb. 5; (2001); p. 1225 - 1230, View in Reaxys 9 of 63

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

propionic acid; hexane

Miyamoto, Shinji; Nakamura, Shinichi; Iwai, Yoshio; Arai, Yasuhiko; Journal of Chemical and Engineering Data; vol. 46; nb. 5; (2001); p. 1225 - 1230, View in Reaxys 10 of 63

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

various solvents

Temperature (Association (MCS)) [°C]

20 - 50

54/428

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Partner (Association (MCS))

Tri-n-octylamine

Sabolova, Erika; Schlosser, Stefan; Martak, Jan; Journal of Chemical and Engineering Data; vol. 46; nb. 3; (2001); p. 735 - 745, View in Reaxys 11 of 63

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

Comment (Association (MCS))

concentration dependence

Partner (Association (MCS))

n-heptane

Wilhelm; Inglese; Grolier; Journal of Chemical Thermodynamics; vol. 31; nb. 9; (1999); p. 1165 - 1174, View in Reaxys 12 of 63

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

Comment (Association (MCS))

concentration dependence

Partner (Association (MCS))

cyclohexane

Wilhelm; Inglese; Grolier; Journal of Chemical Thermodynamics; vol. 31; nb. 9; (1999); p. 1165 - 1174, View in Reaxys 13 of 63

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

Comment (Association (MCS))

concentration dependence

Partner (Association (MCS))

benzene

Wilhelm; Inglese; Grolier; Journal of Chemical Thermodynamics; vol. 31; nb. 9; (1999); p. 1165 - 1174, View in Reaxys 14 of 63

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

H2O

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

alpha cyclodextrin

Castronuovo, Giuseppina; Elia, Vittorio; Niccoli, Marcella; Velleca, Filomena; Viscardi, Giuseppe; Carbohydrate Research; vol. 306; nb. 1-2; (1998); p. 147 - 155, View in Reaxys 15 of 63

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

H2O

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

alpha cyclodextrin

55/428

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Castronuovo, Giuseppina; Elia, Vittorio; Niccoli, Marcella; Velleca, Filomena; Viscardi, Giuseppe; Carbohydrate Research; vol. 306; nb. 1-2; (1998); p. 147 - 155, View in Reaxys 16 of 63

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

H2O

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

alpha cyclodextrin

Castronuovo, Giuseppina; Elia, Vittorio; Niccoli, Marcella; Velleca, Filomena; Viscardi, Giuseppe; Carbohydrate Research; vol. 306; nb. 1-2; (1998); p. 147 - 155, View in Reaxys 17 of 63

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

acetonitrile

Partner (Association (MCS))

pyridine

Mochizuki, Shunsuke; Usui, Yoshiharu; Wakisaka, Akihiro; Chemistry Letters; nb. 11; (1997); p. 1097 - 1098, View in Reaxys 18 of 63

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

acetonitrile

Partner (Association (MCS))

1,4-pyrazine

Mochizuki, Shunsuke; Usui, Yoshiharu; Wakisaka, Akihiro; Chemistry Letters; nb. 11; (1997); p. 1097 - 1098, View in Reaxys 19 of 63

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

dimethylformamide

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

3-(3-Butyl-ureido)-propionic acid 4-nitro-phenyl ester

Ercolani, Gianfranco; Scripilliti, Alessia; Tetrahedron Letters; vol. 37; nb. 1; (1996); p. 101 - 104, View in Reaxys 20 of 63

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

cyclohexane

Partner (Association (MCS))

α-carboline

Chang, Chen-Pin; Yen, Fu-Hsiang; Chou, Pi-Tai; Wei, Ching-Yen; Journal of the Chinese Chemical Society; vol. 43; nb. 6; (1996); p. 463 - 472, View in Reaxys 21 of 63

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

H2O

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

mono-6-deoxy-6-lt;p-(dimethylamino)benzoylaminogt;-α-cyclodextrin

56/428

2017-08-01 04:43:04

Hamasaki, Keita; Ueno, Akihiko; Toda, Fujio; Suzuki, Iwao; Osa, Tetsuo; Bulletin of the Chemical Society of Japan; vol. 67; nb. 2; (1994); p. 516 - 523, View in Reaxys 22 of 63

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

H2O

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

mono-6-deoxy-6-lt;p-(dimethylamino)benzoylaminogt;-β-cyclodextrin

Hamasaki, Keita; Ueno, Akihiko; Toda, Fujio; Suzuki, Iwao; Osa, Tetsuo; Bulletin of the Chemical Society of Japan; vol. 67; nb. 2; (1994); p. 516 - 523, View in Reaxys 23 of 63

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

H2O

Partner (Association (MCS))

N,N-dimethyl-formamide

Sindreu, R. J.; Moya, M. L.; Burgos, F. Sanchez; Gonzalez, A. G.; Journal of Solution Chemistry; vol. 23; nb. 10; (1994); p. 1101 - 1110, View in Reaxys 24 of 63

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

various solvent(s)

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

human serum albumin

Aki; Yamamoto; Journal of Pharmaceutical Sciences; vol. 83; nb. 12; (1994); p. 1712 - 1716, View in Reaxys 25 of 63

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

H2O

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

β-CD; bilirubin

Kano, Koji; Yoshiyasu, Kazuhiro; Yasuoka, Hitoshi; Hata, Sachiko; Hashimoto, Shizunobu; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 8; (1992); p. 1265 - 1269, View in Reaxys 26 of 63

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

cyclohexane

Temperature (Association (MCS)) [°C]

22.9 - 24.9

Partner (Association (MCS))

pyridine N-oxide

Kolling, Orland W.; Journal of Physical Chemistry; vol. 96; nb. 4; (1992); p. 1729 - 1733, View in Reaxys 27 of 63

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

H2O; various solvent(s)

57/428

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Comment (Association (MCS))

Ratio of solvents: 84.78:15.22

Partner (Association (MCS))

potassium n-butyrate

Shevtsova, I. Ya.; Baranov, N. A.; Chernyak, A. S.; J. Gen. Chem. USSR (Engl. Transl.); vol. 62; nb. 10.1; (1992); p. 2194 - 2199,1807 - 1811, View in Reaxys 28 of 63

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

methanol; various solvent(s)

Comment (Association (MCS))

Ratio of solvents: 1:19

Partner (Association (MCS))

potassium n-butyrate

Shevtsova, I. Ya.; Baranov, N. A.; Chernyak, A. S.; J. Gen. Chem. USSR (Engl. Transl.); vol. 62; nb. 10.1; (1992); p. 2194 - 2199,1807 - 1811, View in Reaxys 29 of 63

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

various solvent(s)

Partner (Association (MCS))

water

Shevtsova, I. Ya.; Baranov, N. A.; Chernyak, A. S.; J. Gen. Chem. USSR (Engl. Transl.); vol. 62; nb. 10.1; (1992); p. 2194 - 2199,1807 - 1811, View in Reaxys 30 of 63

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

various solvent(s)

Partner (Association (MCS))

methanol

Shevtsova, I. Ya.; Baranov, N. A.; Chernyak, A. S.; J. Gen. Chem. USSR (Engl. Transl.); vol. 62; nb. 10.1; (1992); p. 2194 - 2199,1807 - 1811, View in Reaxys 31 of 63

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

N-butylamine

Saeten, Jens Olav; Sjoeblom, Johan; Gestblom, Bo; Journal of Physical Chemistry; vol. 95; nb. 3; (1991); p. 1449 - 1453, View in Reaxys 32 of 63

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

heptane

Partner (Association (MCS))

N-butylamine

Saeten, Jens Olav; Sjoeblom, Johan; Gestblom, Bo; Journal of Physical Chemistry; vol. 95; nb. 3; (1991); p. 1449 - 1453, View in Reaxys 33 of 63

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

CDCl3

Partner (Association (MCS))

N-methylcyclohexylamine

58/428

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Kraemer, Rainer; Lang, Rudolph; Brzezinski, Bogumil; Zundel, Georg; Journal of the Chemical Society, Faraday Transactions; vol. 86; nb. 4; (1990); p. 627 - 630, View in Reaxys 34 of 63

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 35 of 63

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

CCl4

Partner (Association (MCS))

didodecyl phosphate

Novikova, L. S.; Shagidullin, R. R.; Ashrafullina, L. Kh.; Eniseenkov, V. N.; Ivanov, B. E.; Russian Journal of Physical Chemistry; vol. 64; nb. 6; (1990); p. 842 - 845; Zhurnal Fizicheskoi Khimii; vol. 64; (1990); p. 1574 - 1578, View in Reaxys 36 of 63

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

solid

Partner (Association (MCS))

Deoxycholic acid

Davies, J. Eric D.; Knott, Vivienne A.; Journal of Molecular Structure; vol. 174; (1988); p. 229 - 234, View in Reaxys 37 of 63

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

Partner (Association (MCS))

H2O

Salomon, Mark; Journal of Solution Chemistry; vol. 15; nb. 3; (1986); p. 237 - 242, View in Reaxys; Harris, Alexander L.; Thompson, Peter T.; Wood, Robert H.; Journal of Solution Chemistry; vol. 9; (1980); p. 305 - 324, View in Reaxys 38 of 63

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

Partner (Association (MCS))

toluene

Hegazi, Mohamed M. Fahmi; Bulletin of the Chemical Society of Japan; vol. 59; (1986); p. 3945 - 3950, View in Reaxys 39 of 63

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

Partner (Association (MCS))

nitrobenzene

Hegazi, Mohamed M. Fahmi; Bulletin of the Chemical Society of Japan; vol. 59; (1986); p. 3945 - 3950, View in Reaxys 40 of 63

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

59/428

2017-08-01 04:43:04

Solvent (Association (MCS))

cyclohexane

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

triethylamine

Kapuku, F.; Huyskens, P. L.; Bulletin des Societes Chimiques Belges; vol. 93; nb. 10; (1984); p. 875 - 890, View in Reaxys 41 of 63

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

cyclohexane

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

tributyl-amine

Kapuku, F.; Huyskens, P. L.; Bulletin des Societes Chimiques Belges; vol. 93; nb. 10; (1984); p. 875 - 890, View in Reaxys 42 of 63

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

2,2,4-trimethyl-pentane

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

griseofulvin

Mehdizadeh; Grant; Journal of Pharmaceutical Sciences; vol. 73; nb. 9; (1984); p. 1195 - 1203, View in Reaxys 43 of 63

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

26.5

Partner (Association (MCS))

H2O

Kaatze; Woermann; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 86; nb. 1; (1982); p. 81 - 87, View in Reaxys 44 of 63

Description (Association Dipole moment of the complex (MCS)) Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

triethylamine

Huyskens, P. L.; Haulait-Pirson, M. Cl.; Kapuku, F.; Bulletin des Societes Chimiques Belges; vol. 89; nb. 7; (1980); p. 505 - 514, View in Reaxys 45 of 63

Description (Association Dipole moment of the complex (MCS)) Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

tributyl-amine

Huyskens, P. L.; Haulait-Pirson, M. Cl.; Kapuku, F.; Bulletin des Societes Chimiques Belges; vol. 89; nb. 7; (1980); p. 505 - 514, View in Reaxys 46 of 63

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

60/428

2017-08-01 04:43:04

Temperature (Association (MCS)) [°C]

15 - 35

Partner (Association (MCS))

cholesteryl chloride; cholesteryl oleate

Panikarskaya, V. D.; Tishchenko, V. G.; Lisetskii, L. N.; Russian Journal of Physical Chemistry; vol. 54; nb. 5; (1980); p. 656 - 658; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 5; (1980); p. 1147 - 1150, View in Reaxys 47 of 63

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

20 - 40

Partner (Association (MCS))

cholesteryl formate; cholesteryl benzoate; cholesteryl oleate

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

nematic-cholesteric mixture

Lisetskii, L. N.; Antonyan, T. P.; Russian Journal of Physical Chemistry; vol. 54; nb. 5; (1980); p. 658 - 660; Zhurnal Fizicheskoi Khimii; vol. 54; nb. 5; (1980); p. 1151 - 1154, View in Reaxys 49 of 63

Description (Association Association with compound (MCS)) Shkredova; Umreiko; Journal of Applied Spectroscopy; vol. 27; (1977); p. 1481, View in Reaxys; Fialkov; Russian Journal of Physical Chemistry; vol. 37; (1963); p. 1051; ; p. 1938, View in Reaxys; Sterk; Monatshefte fuer Chemie; vol. 99; nb. 1; (1968); p. 457, View in Reaxys; Kreshkov et al.; Russian Journal of Physical Chemistry; vol. 42; (1968); p. 153; ; p. 284, View in Reaxys; Chifu; Albu; Annali di Chimica (Rome, Italy); vol. 65; (1975); p. 519, View in Reaxys; Rozenberg; Journal of Applied Spectroscopy; vol. 30; (1979); p. 683, View in Reaxys; Deshmukh et al.; Molecular Physics; vol. 36; (1978); p. 1721,1722,1724,1728, View in Reaxys; Ling et al.; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1966); p. 293,295, View in Reaxys; Seshagiri Rao; Ramachandra Rao; Journal of Scientific and Industrial Research, Section B: Physical Sciences; vol. 21; (1962); p. 331, View in Reaxys

50 of 63

Description (Association Spectrum of the complex (MCS)) Lancelot; Journal of the American Chemical Society; vol. 99; (1977); p. 7037, View in Reaxys; Shimizu; Fujiwara; Chemical and Pharmaceutical Bulletin; vol. 8; (1960); p. 272, View in Reaxys

51 of 63

Description (Association Further physical properties of the complex (MCS)) Davis; Paabo; Journal of Organic Chemistry; vol. 31; (1966); p. 1804,1805, View in Reaxys; Usmanov; Salikhov; Russian Journal of Physical Chemistry; vol. 47; (1973); p. 1426; ; p. 2532, View in Reaxys

52 of 63

Description (Association Stability constant of the complex with ... (MCS)) Magon et al.; Journal of Inorganic and Nuclear Chemistry; vol. 34; (1972); p. 1971,1974, View in Reaxys; Portanova et al.; Journal of Inorganic and Nuclear Chemistry; vol. 34; (1972); p. 1685,1689, View in Reaxys

53 of 63

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

benzene

Partner (Association (MCS))

lead (II)-butyrate

Putilowa; Mjagkowa; Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation); vol. 32; (1959); p. 1319,1321;engl.Ausg.S.1352, View in Reaxys 54 of 63

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

naphthalene

61/428

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Partner (Association (MCS))

lead (II)-butyrate

Putilowa; Mjagkowa; Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation); vol. 32; (1959); p. 1319,1321;engl.Ausg.S.1352, View in Reaxys 55 of 63

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

benzene

Partner (Association (MCS))

water; water

Putilowa; Mjagkowa; Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation); vol. 32; (1959); p. 1319,1321;engl.Ausg.S.1352, View in Reaxys 56 of 63

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

chloral

Sjusjaew et al.; Izv.Akad.Turkmensk.S.S.R.; nb. 3; (1958); p. 10; Chem.Abstr.; (1958); p. 19376, View in Reaxys; Udowenko; Chomenko; Zhurnal Obshchei Khimii; vol. 27; (1957); p. 583; engl. Ausg. S. 649, View in Reaxys 57 of 63

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

pyridine

Schwab; Glatzer; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 61; (1957); p. 1028,1040, View in Reaxys; Lakshmanan; Journal of the Indian Institute of Science, Section A; vol. 36; (1954); p. 218,220; Proceedings - Indian Academy of Sciences, Section A; vol. 43; (1956); p. 152, View in Reaxys; Balachandran; Journal of the Indian Institute of Science, Section A; vol. 36; (1954); p. 10,13, View in Reaxys 58 of 63

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

N-methylaniline

Angelescu; Hoelszky; Anal.Univ.Bukarest; nb. 12; (1956); p. 77,92; Chem.Abstr.; (1958); p. 19896, View in Reaxys; Angelescu; Hoelszky; Acad.Romine Bulet.stiint.<A>; vol. 2; (1950); p. 241; Chem.Abstr.; (1951); p. 8833, View in Reaxys 59 of 63

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

N,N-dimethyl-aniline

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

N-ethyl-N-phenylamine

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

N,N-diethylaniline

62/428

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62 of 63

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

acetamide

Rudenko et al.; Zhurnal Obshchei Khimii; vol. 25; (1955); p. 2430,2432;engl.Ausg.S.2311, View in Reaxys 63 of 63

Description (Association Association with compound (MCS)) Comment (Association (MCS))

Verbindungen 2:1 und 3:1.

Partner (Association (MCS))

tin(IV) chloride

Jakowlewa; Sumarokowa; Izv.Akad.Kazachsk.S.S.R.Ser.chim.; nb. 6; (1953); p. 39,44; Chem.Abstr.; (1954); p. 3835, View in Reaxys Azeotropes (MCS) (96) 1 of 96

Temperature (Azeotropes (MCS)) [°C]

106.1

Pressure (Azeotropes (MCS)) [Torr]

100

Azeotropes

decane

Shleinikova, M.V.; Ovodova, N.P.; Kushner, T.M.; Russian Journal of Physical Chemistry; vol. 59; nb. 12; (1985); p. 1791 - 1793; Zhurnal Fizicheskoi Khimii; vol. 59; (1985); p. 2990 - 2993, View in Reaxys 2 of 96

Temperature (Azeotropes (MCS)) [°C]

125.1

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

octanol

Temperature (Azeotropes (MCS)) [°C]

85.6

Pressure (Azeotropes (MCS)) [Torr]

100

Azeotropes

n-Nonane

Temperature (Azeotropes (MCS)) [°C]

144.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

n-Nonane

Temperature (Azeotropes (MCS)) [°C]

156.9

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

decane

Schelesnjak; Zhurnal Fizicheskoi Khimii; vol. 35; (1961); p. 322; engl. Ausgabe; p. 155, View in Reaxys; Shelesnjak; Levin; Trudy Inst. Neftechim. Protsesow; nb. 1; (1960); p. 95,96-104; Chem.Abstr.; nb. 63; (1962), View in Reaxys; Kushner et al.; Russian Journal of Physical Chemistry; vol. 42; (1968); p. 1189; ; p. 2248,

63/428

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View in Reaxys; Radwan; Hanna; Journal of Chemical and Engineering Data; vol. 21; (1976); p. 285,286,287,288, View in Reaxys 7 of 96

Azeotropes

pyridine

Zieborak; Wyrzykowa-Stankiewicz; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 6; (1958); p. 517,519, View in Reaxys 8 of 96

Azeotropes

undecane

Zieborak; Wyrzykowa-Stankiewicz; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 6; (1958); p. 517,519, View in Reaxys 9 of 96

Temperature (Azeotropes (MCS)) [°C]

172

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

<3-methoxy-butyl>-acetate

Lecat,M.; Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.11, View in Reaxys; Lecat; Annales de Chimie (Cachan, France); vol. <12> 2; (1947); p. 158,168, 186; Mem. Acad. Belg. 8grad; vol. 23; nb. 3; (1949); p. 3,32, View in Reaxys 10 of 96

Temperature (Azeotropes (MCS)) [°C]

164.3

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

<2-ethoxy-ethyl>-acetate

Temperature (Azeotropes (MCS)) [°C]

145.6

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

1.1.2.2-tetrachloro-ethane

Lecat,M.; Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.15, View in Reaxys; Lecat; Annales de Chimie (Cachan, France); vol. <12> 2; (1947); p. 158,168, 186; Mem. Acad. Belg. 8grad; vol. 23; nb. 3; (1949); p. 3,32, View in Reaxys 12 of 96

Temperature (Azeotropes (MCS)) [°C]

157.4

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

bromoacetic acid ethyl ester

Lecat,M.; Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.10, View in Reaxys; Lecat; Annales de Chimie (Cachan, France); vol. <12> 2; (1947); p. 158,168, 186; Mem. Acad. Belg. 8grad; vol. 23; nb. 3; (1949); p. 3,32, View in Reaxys 13 of 96

Temperature (Azeotropes (MCS)) [°C]

161.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

chloroacetic acid propyl ester

Temperature (Azeotropes (MCS)) [°C]

157

Pressure (Azeotropes (MCS)) [Torr]

760

64/428

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Azeotropes

dichloroacetic acid ethyl ester

Azeotropes

trichloroacetic acid ethyl ester

Temperature (Azeotropes (MCS)) [°C]

152.9

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

anisole

Lecat; Ann.Soc.scient.Bruxelles; vol. 47 I; (1927); p. 153, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.25, View in Reaxys; Lecat; Annales de Chimie (Cachan, France); vol. <12> 2; (1947); p. 158,168, 186; Mem. Acad. Belg. 8grad; vol. 23; nb. 3; (1949); p. 3,32, View in Reaxys 17 of 96

Temperature (Azeotropes (MCS)) [°C]

152.3

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

camphene

Lecat; Ann.Soc.scient.Bruxelles; vol. 47 I; (1927); p. 153, View in Reaxys; Lecat; Annales de Chimie (Cachan, France); vol. <12> 2; (1947); p. 158,168, 186; Mem. Acad. Belg. 8grad; vol. 23; nb. 3; (1949); p. 3,32, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.21, View in Reaxys 18 of 96

Temperature (Azeotropes (MCS)) [°C]

137.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

p-xylene

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 110 - 112, View in Reaxys; Lecat; Annales de Chimie (Cachan, France); vol. <12> 2; (1947); p. 158,168, 186; Mem. Acad. Belg. 8grad; vol. 23; nb. 3; (1949); p. 3,32, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.21, View in Reaxys 19 of 96

Temperature (Azeotropes (MCS)) [°C]

163.7

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

indene

Lecat; Annales de Chimie (Cachan, France); vol. <12> 2; (1947); p. 158,168, 186; Mem. Acad. Belg. 8grad; vol. 23; nb. 3; (1949); p. 3,32, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.21, View in Reaxys 20 of 96

Azeotropes

octane

Temperature (Azeotropes (MCS)) [°C]

152.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

bromobenzene

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 35,40, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.15, View in Reaxys; Lecat; Annales de Chimie (Cachan, France); vol. <12> 2; (1947); p. 158,168, 186; Mem. Acad. Belg. 8grad; vol. 23; nb. 3; (1949); p. 3,32, View in Reaxys 22 of 96

Temperature (Azeotropes (MCS)) [°C]

99.4

65/428

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Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

water

Lecat,M.; Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.7, View in Reaxys; Lecat; Annales de Chimie (Cachan, France); vol. <12> 2; (1947); p. 158,168, 186; Mem. Acad. Belg. 8grad; vol. 23; nb. 3; (1949); p. 3,32, View in Reaxys 23 of 96

Temperature (Azeotropes (MCS)) [°C]

143.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

styrene

Temperature (Azeotropes (MCS)) [°C]

138.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

m-xylene

Temperature (Azeotropes (MCS)) [°C]

143

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

o-xylene

Temperature (Azeotropes (MCS)) [°C]

161

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

p-cymene

Temperature (Azeotropes (MCS)) [°C]

154.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

propylbenzene

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 18 - 22, View in Reaxys; Lecat; Annales de Chimie (Cachan, France); vol. <12> 2; (1947); p. 158,168, 186; Mem. Acad. Belg. 8grad; vol. 23; nb. 3; (1949); p. 3,32, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.21, View in Reaxys 28 of 96

Temperature (Azeotropes (MCS)) [°C]

159.4

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

furfural

Lecat,M.; Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.2, View in Reaxys; Lecat; Annales de Chimie (Cachan, France); vol. <12> 2; (1947); p. 158,168, 186; Mem. Acad. Belg. 8grad; vol. 23; nb. 3; (1949); p. 3,32, View in Reaxys 29 of 96

Temperature (Azeotropes (MCS)) [°C]

162.4

66/428

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Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

phenetole

Lecat,M.; Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.25, View in Reaxys; Lecat; Annales de Chimie (Cachan, France); vol. <12> 2; (1947); p. 158,168, 186; Mem. Acad. Belg. 8grad; vol. 23; nb. 3; (1949); p. 3,32, View in Reaxys 30 of 96

Temperature (Azeotropes (MCS)) [°C]

150.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

α-pinene

Temperature (Azeotropes (MCS)) [°C]

156

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

β-pinene

Temperature (Azeotropes (MCS)) [°C]

160.9

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

dipentene

Temperature (Azeotropes (MCS)) [°C]

158

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

mesitylene

Temperature (Azeotropes (MCS)) [°C]

146.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

bromoform

Temperature (Azeotropes (MCS)) [°C]

163.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

iodobenzene

Temperature (Azeotropes (MCS)) [°C]

162.5

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Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

terpinolene

Temperature (Azeotropes (MCS)) [°C]

129.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

butyl iodide

Temperature (Azeotropes (MCS)) [°C]

160.7

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

α-terpinene

Temperature (Azeotropes (MCS)) [°C]

162.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

butylbenzene

Temperature (Azeotropes (MCS)) [°C]

131.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

chlorobenzene

Temperature (Azeotropes (MCS)) [°C]

159.1

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

diiodomethane

Temperature (Azeotropes (MCS)) [°C]

151.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

hexyl bromide

68/428

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43 of 96

Temperature (Azeotropes (MCS)) [°C]

156.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

pentachloroethane

Temperature (Azeotropes (MCS)) [°C]

135.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

ethylbenzene

Temperature (Azeotropes (MCS)) [°C]

161.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

benzyl chloride

Temperature (Azeotropes (MCS)) [°C]

163

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

2-bromo-toluene

Temperature (Azeotropes (MCS)) [°C]

163.6

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

3-bromo-toluene

Temperature (Azeotropes (MCS)) [°C]

163.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

4-bromo-toluene

Temperature (Azeotropes (MCS)) [°C]

144.4

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isopentyl iodide

69/428

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Temperature (Azeotropes (MCS)) [°C]

154.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

2-chloro-toluene

Temperature (Azeotropes (MCS)) [°C]

156.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

4-chloro-toluene

Temperature (Azeotropes (MCS)) [°C]

147.9

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isopentyl nitrate

Temperature (Azeotropes (MCS)) [°C]

149.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isopropylbenzene

Azeotropes

diisobutyl sulfide

Lecat,M.; Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.30, View in Reaxys; Lecat; Annales de Chimie (Cachan, France); vol. <12> 2; (1947); p. 158,168, 186; Mem. Acad. Belg. 8grad; vol. 23; nb. 3; (1949); p. 3,32, View in Reaxys 55 of 96

Temperature (Azeotropes (MCS)) [°C]

161.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

diisopentyl ether

Temperature (Azeotropes (MCS)) [°C]

131.1

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

1.2-dibromo-ethane

70/428

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Temperature (Azeotropes (MCS)) [°C]

138.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

1.2-dibromo-propane

Temperature (Azeotropes (MCS)) [°C]

158.4

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

1.3-dibromo-propane

Temperature (Azeotropes (MCS)) [°C]

162.4

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

pyruvic acid

Lecat,M.; Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.1, View in Reaxys; Lecat; Annales de Chimie (Cachan, France); vol. <12> 2; (1947); p. 158,168, 186; Mem. Acad. Belg. 8grad; vol. 23; nb. 3; (1949); p. 3,32, View in Reaxys 60 of 96

Temperature (Azeotropes (MCS)) [°C]

160

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

methylbenzyl ether

Temperature (Azeotropes (MCS)) [°C]

152.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

2.7-dimethyl-octane

Temperature (Azeotropes (MCS)) [°C]

121

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

tetrachloroethylene

Temperature (Azeotropes (MCS)) [°C]

163

71/428

2017-08-01 04:43:04

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

1.2-dichloro-benzene

Temperature (Azeotropes (MCS)) [°C]

162

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

1.4-dichloro-benzene

Temperature (Azeotropes (MCS)) [°C]

159.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

1.2.4-trimethylbenzene

Temperature (Azeotropes (MCS)) [°C]

152

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

1.2.3-trichloro-propane

Azeotropes

oxalic acid dimethyl ester

Lecat,M.; Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.8, View in Reaxys; Lecat; Annales de Chimie (Cachan, France); vol. <12> 2; (1947); p. 158,168, 186; Mem. Acad. Belg. 8grad; vol. 23; nb. 3; (1949); p. 3,32, View in Reaxys 68 of 96

Temperature (Azeotropes (MCS)) [°C]

129

Pressure (Azeotropes (MCS)) [Torr]

100

Azeotropes

N.N-dimethyl-butyramide

Ruhoff; Reid; Journal of the American Chemical Society; vol. 59; (1937); p. 402, View in Reaxys 69 of 96

Temperature (Azeotropes (MCS)) [°C]

161

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

indene

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 110 - 112, View in Reaxys 70 of 96

Temperature (Azeotropes (MCS)) [°C]

142

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

o-xylene

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 18 - 22, View in Reaxys

72/428

2017-08-01 04:43:04

71 of 96

Temperature (Azeotropes (MCS)) [°C]

160

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

p-cymene

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 110 - 112, View in Reaxys 72 of 96

Temperature (Azeotropes (MCS)) [°C]

150.3

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

α-pinene

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 110 - 112, View in Reaxys 73 of 96

Temperature (Azeotropes (MCS)) [°C]

147.6

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

bromoform

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 18 - 22, View in Reaxys 74 of 96

Temperature (Azeotropes (MCS)) [°C]

154

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

diisopentyl

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 18 - 22, View in Reaxys 75 of 96

Temperature (Azeotropes (MCS)) [°C]

160.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

d-limonene

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 35,40, View in Reaxys 76 of 96

Temperature (Azeotropes (MCS)) [°C]

159

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

pseudocumene

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 35,40, View in Reaxys 77 of 96

Temperature (Azeotropes (MCS)) [°C]

135.9

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

ethylbenzene

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 35,40, View in Reaxys 78 of 96

Temperature (Azeotropes (MCS)) [°C]

160

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isopentyl ether

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 18 - 22, View in Reaxys

73/428

2017-08-01 04:43:04

79 of 96

Temperature (Azeotropes (MCS)) [°C]

161.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

4-bromo-toluene

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 18 - 22, View in Reaxys 80 of 96

Temperature (Azeotropes (MCS)) [°C]

160.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

benzyl chloride

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 110 - 112, View in Reaxys 81 of 96

Temperature (Azeotropes (MCS)) [°C]

161.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

2-bromo-toluene

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 35,40, View in Reaxys 82 of 96

Temperature (Azeotropes (MCS)) [°C]

162

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

hexachloroethane

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 110 - 112, View in Reaxys 83 of 96

Temperature (Azeotropes (MCS)) [°C]

153

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

1.2.3-trichloro-propane

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 18 - 22, View in Reaxys 84 of 96

Temperature (Azeotropes (MCS)) [°C]

157.6

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

mesitylene

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; (1929); p. 110 - 112, View in Reaxys 85 of 96

Temperature (Azeotropes (MCS)) [°C]

159.4

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

furfurol

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 86 of 96

Temperature (Azeotropes (MCS)) [°C]

160.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

phenetole

Lecat; Ann.Soc.scient.Bruxelles; vol. 48 I; (1928); p. 19, View in Reaxys

74/428

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87 of 96

Temperature (Azeotropes (MCS)) [°C]

161.6

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

iodobenzene

Lecat; Ann.Soc.scient.Bruxelles; vol. 48 I; (1928); p. 118,119, View in Reaxys 88 of 96

Temperature (Azeotropes (MCS)) [°C]

145.6

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isopentyl iodide

Lecat; Ann.Soc.scient.Bruxelles; vol. 48 I; (1928); p. 118,119, View in Reaxys 89 of 96

Temperature (Azeotropes (MCS)) [°C]

154

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

2-chloro-toluene

Lecat; Ann.Soc.scient.Bruxelles; vol. 48 I; (1928); p. 118,119, View in Reaxys 90 of 96

Temperature (Azeotropes (MCS)) [°C]

155.7

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

4-chloro-toluene

Lecat; Ann.Soc.scient.Bruxelles; vol. 48 I; (1928); p. 118,119, View in Reaxys 91 of 96

Temperature (Azeotropes (MCS)) [°C]

160

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

1.4-dichloro-benzene

Lecat; Ann.Soc.scient.Bruxelles; vol. 48 I; (1928); p. 118,119, View in Reaxys 92 of 96

Temperature (Azeotropes (MCS)) [°C]

138.3

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

m-xylene

Lecat; Ann.Soc.scient.Bruxelles; vol. 47 I; (1927); p. 153, View in Reaxys 93 of 96

Temperature (Azeotropes (MCS)) [°C]

131.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

chlorobenzene

Lecat; Ann.Soc.scient.Bruxelles; vol. 47 I; (1927); p. 153, View in Reaxys 94 of 96

Temperature (Azeotropes (MCS)) [°C]

131.1

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

ethylene bromide

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

75/428

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95 of 96

Temperature (Azeotropes (MCS)) [°C]

145.7

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

1.1.2.2-tetrachloro-ethane

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

Temperature (Azeotropes (MCS)) [°C]

142.6

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

bromoform

Holley; Weaver; Journal of the American Chemical Society; vol. 27; (1905); p. 1051,1056, View in Reaxys Boundary Surface Phenomena (MCS) (51) 1 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Temperature (Boundary Surface Phenomena (MCS)) [°C]

Partner (Boundary Surface Phenomena (MCS))

H2O

Granados, Karla; Gracia-Fadrique, Jesus; Amigo, Alfredo; Bravo, Ramon; Journal of Chemical and Engineering Data; vol. 51; nb. 4; (2006); p. 1356 - 1360, View in Reaxys 2 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Solvent (Boundary Surface Phenomena (MCS))

H2O

Comment (Boundary Surface Phenomena (MCS))

concentration dependence

Partner (Boundary Surface Phenomena (MCS))

hexadecylammonium acetate

Mitina; Dikhtievskaya; Mozheiko; Russian Journal of Applied Chemistry; vol. 73; nb. 10; (2000); p. 1712 - 1716, View in Reaxys 3 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Temperature (Boundary Surface Phenomena (MCS)) [°C]

25.1 - 35

Partner (Boundary Surface Phenomena (MCS))

cyclohexane

Kaur, Satindar; Lark, Bhajan S.; Aggarwal, Suresh K.; Singh, Surjit; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 35; nb. 10; (1996); p. 832 - 835, View in Reaxys 4 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Temperature (Boundary Surface Phenomena (MCS)) [°C]

25 - 35

76/428

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Partner (Boundary Surface Phenomena (MCS))

octanol

Description (Boundary Surface Phenomena (MCS))

Surface tension

Temperature (Boundary Surface Phenomena (MCS)) [°C]

25 - 35

Partner (Boundary Surface Phenomena (MCS))

benzene

Description (Boundary Surface Phenomena (MCS))

Surface tension

Temperature (Boundary Surface Phenomena (MCS)) [°C]

25 - 35

Partner (Boundary Surface Phenomena (MCS))

toluene

Description (Boundary Surface Phenomena (MCS))

Surface tension

Temperature (Boundary Surface Phenomena (MCS)) [°C]

25 - 35

Partner (Boundary Surface Phenomena (MCS))

tetrachloromethane

Description (Boundary Surface Phenomena (MCS))

Surface tension

Temperature (Boundary Surface Phenomena (MCS)) [°C]

25 - 35

Partner (Boundary Surface Phenomena (MCS))

chloroform

Description (Boundary Surface Phenomena (MCS))

Surface tension

Temperature (Boundary Surface Phenomena (MCS)) [°C]

25 - 35

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Partner (Boundary Surface Phenomena (MCS))

methanol

Description (Boundary Surface Phenomena (MCS))

Surface tension

Temperature (Boundary Surface Phenomena (MCS)) [°C]

25 - 35

Partner (Boundary Surface Phenomena (MCS))

acetone

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

nitromethane

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Partner (Boundary Surface Phenomena (MCS))

acetic acid butyl ester; H2O

Ermakov, A. A.; Danilov, V. A.; Kon'shin, Yu. A.; Russian Journal of Physical Chemistry; vol. 65; nb. 1; (1991); p. 114 - 116; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p. 223 - 226, View in Reaxys 13 of 51

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Partner (Boundary Surface Phenomena (MCS))

chloroform; H2O

Description (Boundary Surface Phenomena (MCS))

Surface tension

Kusnezow; Smirnow; J. Appl. Chem. USSR (Engl. Transl.); vol. 34; (1961); p. 1954,1859; Chem.Abstr.; nb. 3318; (1962), View in Reaxys; Abramzon et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 46; (1976); p. 1609,1566,1567, View in Reaxys; Wright; Akhtar; Journal of the Chemical Society [Section] B: Physical Organic; (1970); p. 151,152-153, View in Reaxys 15 of 51

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Shain; Prausnitz; AIChE Journal; vol. 10; (1964); p. 766, View in Reaxys 16 of 51

Description (Boundary Surface Phenomena (MCS))

Boundary surface phenomena

Waksmundzki; Ratajewicz; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 9; (1961); p. 451, View in Reaxys

78/428

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17 of 51

Description (Boundary Surface Phenomena (MCS))

Contact angle with compound

Temperature (Boundary Surface Phenomena (MCS)) [°C]

Partner (Boundary Surface Phenomena (MCS))

α aluminium oxide

Hare; Zisman; Journal of Physical Chemistry; vol. 59; (1955); p. 335,336, View in Reaxys 18 of 51

Description (Boundary Surface Phenomena (MCS))

Surface potential

Comment (Boundary Surface Phenomena (MCS))

monomolekularer Schichten auf wss.Buttersaeure-Loesungen verschiedener Konzentration.

Isemura; Hotta; Bulletin of the Chemical Society of Japan; vol. 23; (1950); p. 193,194, View in Reaxys 19 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Solvent (Boundary Surface Phenomena (MCS))

H2O

Traube; Verh.dtsch.phys.Ges.; vol. 10; (1908); p. 901, View in Reaxys; Weber; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 181; (1929); p. 390, View in Reaxys; Mills; Robinson; Journal of the Chemical Society; (1931); p. 1636, View in Reaxys; Traube; Weber; Guirini; Biochemische Zeitschrift; vol. 217; (1930); p. 403, View in Reaxys; Meissner; Michaels; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2786, View in Reaxys; Weber; Sternglanz; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 169; (1934); p. 244,247, View in Reaxys; Ssementschenko; Iwanowa; Zhurnal Obshchei Khimii; vol. 5; (1935); p. 810; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 1389, View in Reaxys 20 of 51

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

wss.Loesungen gegen Benzol.

Boas-Traube; Volmer; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 178; (1937); p. 329, View in Reaxys; Lazarew; Lawrow; Matwejew; Biochemische Zeitschrift; vol. 217; (1930); p. 458, View in Reaxys; Hutchinson; J.Colloid Sci.; vol. 3; (1948); p. 226; Chem.Abstr.; (1948); p. 6201, View in Reaxys 21 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

nitrobenzene

Aleixandre; Anales de la Real Sociedad Espanola de Fisica y Quimica; vol. 40; (1944); p. 490, View in Reaxys; Ssementschenko; Iwanowa; Zhurnal Obshchei Khimii; vol. 5; (1935); p. 810; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 1389, View in Reaxys 22 of 51

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

gegen Quecksilber.

Gauditz; Ramsauer; Kolloid-Zeitschrift; vol. 109; (1944); p. 126; Chem.Abstr.; (1949); p. 2060, View in Reaxys

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23 of 51

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

von Gemischen mit Cyclohexan gegen Quecksilber.

Gauditz; Ramsauer; Kolloid-Zeitschrift; vol. 109; (1944); p. 126; Chem.Abstr.; (1949); p. 2060, View in Reaxys 24 of 51

Description (Boundary Surface Phenomena (MCS))

Pressure-surface isotherm

Solvent (Boundary Surface Phenomena (MCS))

H2O

Comment (Boundary Surface Phenomena (MCS))

in der monomolekularen Grenzflaechenschicht.

Partner (Boundary Surface Phenomena (MCS))

paraffin

Fowkes; Harkins; Journal of the American Chemical Society; vol. 62; (1940); p. 3381, View in Reaxys 25 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Temperature (Boundary Surface Phenomena (MCS)) [°C]

Partner (Boundary Surface Phenomena (MCS))

acetone

Udowenko; Ssitschkowa; Toropow; Zhurnal Obshchei Khimii; vol. 9; (1939); p. 2049,2050; Chem. Zentralbl.; vol. 112; nb. I; (1941); p. 1411, View in Reaxys 26 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Temperature (Boundary Surface Phenomena (MCS)) [°C]

Partner (Boundary Surface Phenomena (MCS))

acetone

Udowenko; Ssitschkowa; Toropow; Zhurnal Obshchei Khimii; vol. 9; (1939); p. 2049,2050; Chem. Zentralbl.; vol. 112; nb. I; (1941); p. 1411, View in Reaxys 27 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Temperature (Boundary Surface Phenomena (MCS)) [°C]

Partner (Boundary Surface Phenomena (MCS))

acetone

Udowenko; Ssitschkowa; Toropow; Zhurnal Obshchei Khimii; vol. 9; (1939); p. 2049,2050; Chem. Zentralbl.; vol. 112; nb. I; (1941); p. 1411, View in Reaxys 28 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

80/428

2017-08-01 04:43:04

Temperature (Boundary Surface Phenomena (MCS)) [°C]

Partner (Boundary Surface Phenomena (MCS))

2-Pentanone

Udowenko; Ssitschkowa; Toropow; Zhurnal Obshchei Khimii; vol. 9; (1939); p. 2049,2050; Chem. Zentralbl.; vol. 112; nb. I; (1941); p. 1411, View in Reaxys 29 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Temperature (Boundary Surface Phenomena (MCS)) [°C]

Partner (Boundary Surface Phenomena (MCS))

2-Pentanone

Udowenko; Ssitschkowa; Toropow; Zhurnal Obshchei Khimii; vol. 9; (1939); p. 2049,2050; Chem. Zentralbl.; vol. 112; nb. I; (1941); p. 1411, View in Reaxys 30 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Temperature (Boundary Surface Phenomena (MCS)) [°C]

Partner (Boundary Surface Phenomena (MCS))

2-Pentanone

Udowenko; Ssitschkowa; Toropow; Zhurnal Obshchei Khimii; vol. 9; (1939); p. 2049,2050; Chem. Zentralbl.; vol. 112; nb. I; (1941); p. 1411, View in Reaxys 31 of 51

Description (Boundary Surface Phenomena (MCS))

Pressure-surface isotherm

Solvent (Boundary Surface Phenomena (MCS))

H2O

Comment (Boundary Surface Phenomena (MCS))

monomolekulare Schichte.

Partner (Boundary Surface Phenomena (MCS))

n-tetradecanoic acid

Adam; Askew; Pankhurst; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 170; (1939); p. 485,496, View in Reaxys 32 of 51

Description (Boundary Surface Phenomena (MCS))

Surface potential

Comment (Boundary Surface Phenomena (MCS))

monomolekularer Schichten von Myristinsaeure auf wss.Buttersaeure-Loesungen.

Adam; Askew; Pankhurst; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 170; (1939); p. 485,496, View in Reaxys 33 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

81/428

2017-08-01 04:43:04

Solvent (Boundary Surface Phenomena (MCS))

H2O

Comment (Boundary Surface Phenomena (MCS))

bei verschiedenen Temperaturen.

Tamamushi; Kolloid-Zeitschrift; vol. 71; (1935); p. 154, View in Reaxys; Fisher; Mackay; Canadian Journal of Research, Section A: Physical Sciences; vol. 16; (1938); p. 209, View in Reaxys 34 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

o-toluidine

Angelescu; Eustatiu; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 177; (1936); p. 265, View in Reaxys 35 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

1-amino-3-methylbenzene

Angelescu; Eustatiu; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 177; (1936); p. 265, View in Reaxys 36 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

piperidine

Prideaux; Coleman; Journal of the Chemical Society; (1936); p. 1348; Journal of the Chemical Society; (1937); p. 463, View in Reaxys 37 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

3-(1-methyl-pyrrolidin-2-yl)-pyridine

Ssementschenko; Iwanowa; Zhurnal Obshchei Khimii; vol. 5; (1935); p. 810; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 1389, View in Reaxys 38 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

toluene

Merzlin; Trifonow; Zhurnal Fizicheskoi Khimii; vol. 5; (1934); p. 1146; Chem. Zentralbl.; vol. 106; nb. II; (1935); p. 1843, View in Reaxys 39 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

CaCl2

Kosakewitsch; Kosakewitsch; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 166; (1933); p. 113,114, 122, View in Reaxys

82/428

2017-08-01 04:43:04

40 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

naphthalene

Kosakewitsch; Kosakewitsch; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 166; (1933); p. 113,114, 122, View in Reaxys 41 of 51

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

wss.Loesungen gegen Paraffin und gegen Oelsaeure.

Traube; Weber; Guirini; Biochemische Zeitschrift; vol. 217; (1930); p. 403, View in Reaxys 42 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Solvent (Boundary Surface Phenomena (MCS))

H2O

Temperature (Boundary Surface Phenomena (MCS)) [°C]

Rehbinder; Biochemische Zeitschrift; vol. 187; (1927); p. 23, View in Reaxys 43 of 51

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

bei 20grad zwischen Loesungen von Buttersaeure in Wasser und in Hexan.

Harkins; McLaughlin; Journal of the American Chemical Society; vol. 47; (1925); p. 1612, View in Reaxys; Rehbinder; Biochemische Zeitschrift; vol. 187; (1927); p. 23, View in Reaxys 44 of 51

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

bei 20grad zwischen Loesungen von Buttersaeure in Wasser und in Benzol.

Harkins; King; Journal of the American Chemical Society; vol. 41; (1919); p. 984, View in Reaxys; Rehbinder; Biochemische Zeitschrift; vol. 187; (1927); p. 23, View in Reaxys 45 of 51

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

bei 20grad zwischen Loesungen von Buttersaeure in Wasser und in Olivenoel.

Rehbinder; Biochemische Zeitschrift; vol. 187; (1927); p. 23, View in Reaxys 46 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Solvent (Boundary Surface Phenomena (MCS))

H2O

83/428

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Temperature (Boundary Surface Phenomena (MCS)) [°C]

Bartsch; Koll.Beih.; vol. 20; p. 7; Chem. Zentralbl.; vol. 96; nb. I; (1925); p. 2362, View in Reaxys 47 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Solvent (Boundary Surface Phenomena (MCS))

H2O

Temperature (Boundary Surface Phenomena (MCS)) [°C]

0 - 100

Rehbinder; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 111; (1924); p. 453; Biochemische Zeitschrift; vol. 187; (1927); p. 33, View in Reaxys 48 of 51

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

einer 1 prozentigen Buttersaeure-Loesung in Benzol gegen Wasser, 0.02n-Natronlauge und 1prozent Natriumchlorid enthaltende 0.02n-Natronlauge.

Dubrisay; Rev.gen.Colloides; vol. 5; p. 487, View in Reaxys; Dubrisay; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 178; (1924); p. 1976; Bulletin de la Societe Chimique de France; vol. <4>37; (1925); p. 999; Chem. Zentralbl.; vol. 98; nb. II; (1927); p. 396, View in Reaxys 49 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Solvent (Boundary Surface Phenomena (MCS))

H2O

Temperature (Boundary Surface Phenomena (MCS)) [°C]

18.5 - 19

Tominaga; Biochemische Zeitschrift; vol. 140; (1923); p. 245, View in Reaxys 50 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Solvent (Boundary Surface Phenomena (MCS))

H2O

Partner (Boundary Surface Phenomena (MCS))

benzene

Harkins; Humphery; Journal of the American Chemical Society; vol. 38; (1916); p. 243, View in Reaxys 51 of 51

Description (Boundary Surface Phenomena (MCS))

Surface tension

Partner (Boundary Surface Phenomena (MCS))

water

Drucker; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 52; (1905); p. 649, View in Reaxys; von Szyszkowski; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 64; (1908); p. 395, View in Reaxys Chromatographic Data (7) Chromatographic Location data

References

84/428

2017-08-01 04:43:04

GC (Gas chroma- supporting infortography) mation

Lozano, Pedro; Bernal, Juana M.; Navarro, Alicia; Green Chemistry; vol. 14; nb. 11; (2012); p. 3026 - 3033, View in Reaxys; Zhu, Jian Cai; Niu, Yun Wei; Feng, Tao; Liu, Sheng Jiang; Cheng, He Xing; Xu, Na; Yu, Hai Yan; Xiao, Zuo Bing; Natural Product Research; vol. 28; nb. 21; (2014); p. 1887 - 1893, View in Reaxys; Guetat, Arbi; AlGhamdi, Faraj A.; Osman, Ahmed K.; Natural Product Research; vol. 31; nb. 5; (2017); p. 598 - 603, View in Reaxys; Niu, Yunwei; Chen, Xiaomei; Xiao, Zuobing; Ma, Ning; Zhu, Jiancai; Natural Product Research; vol. 31; nb. 8; (2017); p. 938 - 944, View in Reaxys

GC (Gas chromatography)

Wang, Weijun; Zhang, Lanwei; Li, Yanhua; Molecules; vol. 17; nb. 12; (2012); p. 14393 - 14408, View in Reaxys; Garcia-Gonzalez, Diego L.; Aparicio, Ramon; Aparicio-Ruiz, Ramon; Molecules; vol. 18; nb. 4; (2013); p. 3927 - 3947, View in Reaxys; Kim, Jae Yul; Kim, Yeon Ho; Han, Suenghoon; Choi, Sun Hee; Lee, Jae Sung; Journal of Catalysis; vol. 302; (2013); p. 58 - 66, View in Reaxys; Zou, Xiaoqiang; Huang, Jianhua; Jin, Qingzhe; Guo, Zheng; Liu, Yuanfa; Cheong, Lingzhi; Xu, Xuebing; Wang, Xingguo; JAOCS, Journal of the American Oil Chemists' Society; vol. 91; nb. 3; (2014); p. 481 - 495, View in Reaxys; Zhang, Meiling; Deng, Mingjie; Ma, Jianshe; Wang, Xianqin; Chemical and Pharmaceutical Bulletin; vol. 62; nb. 6; (2014); p. 505 507, View in Reaxys; Vacas, Sandra; Abad-Paya, Maria; Primo, Jaime; Navarro-Llopis, Vicente; Journal of Agricultural and Food Chemistry; vol. 62; nb. 26; (2014); p. 6053 - 6064, View in Reaxys; Palomero, Felipe; Bertani, Paolo; Fernández De Simón, Brígida; Cadahía, Estrella; Benito, Santiago; Morata, Antonio; Suárez-Lepe, José A.; Food Chemistry; vol. 171; (2014); p. 212 - 223, View in Reaxys; Rakete, Stefan; Berger, Robert; Böhme, Steffi; Glomb, Marcus A.; Journal of Agricultural and Food Chemistry; vol. 62; nb. 30; (2014); p. 7541 - 7549, View in Reaxys; Patra, Jayanta Kumar; Kim, Sung Hong; Hwang, Hyewon; Choi, Joon Weon; Baek, Kwang-Hyun; Molecules; vol. 20; nb. 3; (2015); p. 3986 - 4006, View in Reaxys; Gianotti; Panseri; Robotti; Benzi; Mazzucco; Gosetti; Frascarolo; Oddone; Baldizzone; Marengo; Chiesa; Journal of Chemistry; vol. 2015; (2015); Art.No: 597471, View in Reaxys; Amer, Bashar; Nebel, Caroline; Bertram, Hanne C.; Mortensen, Grith; Dalsgaard, Trine K.; Lipids; vol. 50; nb. 7; (2015); p. 681 - 689, View in Reaxys; Dong, Juan; Zhao, Wei; Gasmalla, Mohammed A.A.; Sun, Jingtao; Hua, Xiao; Zhang, Wenbin; Han, Liang; Fan, Yuting; Feng, Yinghui; Shen, Qiuyun; Yang, Ruijin; Journal of Molecular Catalysis B: Enzymatic; vol. 121; (2015); p. 53 - 63; Art.No: 3208, View in Reaxys; Mathew, Sindhu; Zakaria, Zainul Akmar; Musa, Nur Fashya; Process Biochemistry; vol. 50; nb. 11; (2015); p. 1985 - 1992, View in Reaxys; Kurtovic, Ivan; Marshall, Susan N.; Cleaver, Helen L.; Miller, Matthew R.; Food Chemistry; vol. 199; (2016); p. 323 - 329, View in Reaxys; Wang, Yuming; Guo, Xuejun; Xie, Jiabin; Hou, Zhiguo; Li, Yubo; McPhee, Derek J.; Molecules; vol. 20; nb. 12; (2015); p. 21364 - 21372, View in Reaxys; Yuan, Fang; Qian, Michael C.; Journal of Agricultural and Food Chemistry; vol. 64; nb. 2; (2016); p. 443 450, View in Reaxys; Franitza, Laura; Granvogl, Michael; Schieberle, Peter; Journal of Agricultural and Food Chemistry; vol. 64; nb. 3; (2016); p. 637 - 645, View in Reaxys; Jun, Yonjin; Lee, Sang Mi; Ju, Hyun Kyoung; Lee, Hong Jin; Choi, Hyung-Kyoon; Jo, Gyeong Suk; Kim, Young-Suk; Molecules; vol. 21; nb. 3; (2016); Art.No: 363, View in Reaxys; Shahdousti, Parvin; Shojaee, Rezvan; Aghamohammadi, Mohammad; Harooni, Behrang; Australian Journal of Chemistry; vol. 69; nb. 4; (2016); p. 451 457, View in Reaxys; Kumari, Asha; Parida, Asish Kumar; RSC Advances; vol. 6; nb. 57; (2016); p. 51629 - 51641, View in Reaxys; Chiesa; Panseri; Bonacci; Procopio; Zecconi; Arioli; Cuevas; Moreno-Rojas; Food Chemistry; vol. 212; (2016); p. 296 304, View in Reaxys; Munafo, John P.; Didzbalis, John; Schnell, Raymond J.; Steinhaus, Martin; Journal of Agricultural and Food Chemistry; vol. 64; nb. 21; (2016); p. 4312 - 4318, View in Reaxys; Mahmoud, Mohamed Ahmed Abbas; Buettner, Andrea; Food Chemistry; vol. 210; (2016); p. 623 - 630, View in Reaxys; Zheng, Yang; Sun, Baoguo; Zhao, Mouming; Zheng, Fuping; Huang, Mingquan; Sun, Jinyuan; Sun, Xiaotao; Li, Hehe; Journal of Agricultural and Food Chemistry; vol. 64; nb. 26; (2016); p. 5367 - 5374, View in Reaxys; Mall, Veronika; Schieberle, Peter; Journal of Agricultural and Food Chemistry; vol. 64; nb. 33; (2016); p. 6433 - 6442, View in Reaxys; Jerković, Igor; Prdun, Saša; Marijanović, Zvonimir; Zekić, Marina; Bubalo, Dragan; Svečnjak, Lidija; Tuberoso, Carlo I. 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ElMissiry; Seif ElNasr; Egyptian Journal of Chemistry; vol. 59; nb. 1; (2016); p. 21 - 31, View in Reaxys; Sha, Sha; Chen, Shuang; Qian, Michael; Wang, Chengcheng; Xu, Yan; Journal of Agricultural and Food Chemistry; vol. 65; nb. 1; (2017); p. 123 - 131, View in Reaxys; Wagner, Juliane; Schieberle, Peter; Granvogl, Michael; Journal of Agricultural and Food Chemistry; vol. 65; nb. 1; (2017); p. 132 - 138, View in Reaxys; Zierer, Bianca; Schieberle, Peter; Granvogl, Michael; Journal of Agricultural and Food Chemistry; vol. 64; nb. 50; (2016); p. 9515 - 9522, View in Reaxys; Zhao, Pengtao; Gao, Jinxin; Qian, Michael; Li, Hua; Molecules; vol. 22; nb. 7; (2017); Art.No: 1045, View in Reaxys HPLC (High performance liquid chromatography)

Hackenschmidt, Silke; Moldenhauer, Eva J.; Behrens, Geoffrey A.; Gand, Martin; Pavlidis, Ioannis V.; Bornscheuer, Uwe T.; ChemCatChem; vol. 6; nb. 4; (2014); p. 1015 - 1020, View in Reaxys; Wang, Zhiyi; Ma, Jianshe; Zhang, Meiling; Wen, Congcong; Huang, Xueli; Sun, Fa; Wang, Shuanghu; Hu, Lufeng; Lin, Guanyang; Wang, Xianqin; Biological and Pharmaceutical Bulletin; vol. 38; nb. 7; (2015); p. 1049 - 1053, View in Reaxys; Wang, Xianqin; Zhang, Meiling; Ma, Jianshe; Zhang, Yuan; Hong, Guangliang; Sun, Fa; Lin, Guanyang; Hu, Lufeng; Biological and Pharmaceutical Bulletin; vol. 38; nb. 3; (2015); p. 470 - 475, View in Reaxys; Jabri, Mohamed-Amine; Hajaji, Soumaya; Marzouki, Lamjed; El-Benna, Jamel; Sakly, Mohsen; Sebai, Hichem; RSC Advances; vol. 6; nb. 20; (2016); p. 16645 - 16655, View in Reaxys

GC (Gas chroma- Paragraph 0115 tography)

Patent; Chonbuk National University Industry-Academic Cooperation Foundation; Lee, Young Hun; Yu, Sang Mi; Lee, Ha Gyoung; Chung, Eui-sun; Yang, Chang Yeol; Choe, Deuk Su; (27 pag.); KR2015/141293; (2015); (A) Korean, View in Reaxys

GC (Gas chroma- Paragraph 0111 tography)

Patent; CHENG, Cecilia; DOBSON, Ian, David; HOGBEN, Andrew, John; LUCY, Andrew, Richard; SUNLEY, John, Glenn; BOLTON, Leslie, William; WO2014/18837; (2014); (A1) English, View in Reaxys

GC (Gas chroma- Page/Page coltography) umn 22

Patent; Université de Lausanne; Broillet, Marie-Christine; Brechbühl, Julien; EP2772487; (2014); (A1) English, View in Reaxys

HPLC (High performance liquid chromatography)

Ni, Yan; Hagedoorn, Peter-Leon; Xu, Jian-He; Arends, Isabel W. C. E.; Hollmann, Frank; Chemical Communications; vol. 48; nb. 99; (2012); p. 12056 - 12058, View in Reaxys

supporting information

Compressibility (3) Description (Com- Comment (Compressibility) pressibility)

References

Isothermal compressibility

Vong; Tsai; Journal of Chemical and Engineering Data; vol. 42; nb. 6; (1997); p. 1116 1120, View in Reaxys; Miyamoto, Shinji; Nakamura, Shinichi; Iwai, Yoshio; Arai, Yasuhiko; Journal of Chemical and Engineering Data; vol. 44; nb. 1; (1999); p. 48 - 51, View in Reaxys

Adiabatic compressibility

Rao; Rao; Current Science; vol. 41; (1972); p. 286, View in Reaxys

Adiabatic compressibility

bei 25grad.

Venkateswaran; Journal of Physical Chemistry; vol. 31; (1927); p. 1523, View in Reaxys

Conformation (1) Object of Investi- References gation Conformation

Taniguchi et al.; Bulletin of the Chemical Society of Japan; vol. 45; (1972); p. 3380,3381,3382, View in Reaxys; Hayashi; Umemura; Journal of Chemical Physics; vol. 63; (1975); p. 1732,1735, View in Reaxys; Kanters et al.; Tetrahedron; vol. 23; (1967); p. 4027,4028,4031, View in Reaxys; Hayashi, Soichi; Umemura, Junzo; Nakamura, Ryoko; Journal of Molecular Structure; vol. 69; (1980); p. 123 - 136, View in Reaxys

Critical Density (1) Critical Density References [g·cm-3] 0.302

Gude, Michael T.; Mendez-Santiago, Janette; Teja, Amyn S.; Journal of Chemical and Engineering Data; vol. 42; nb. 2; (1997); p. 278 - 280, View in Reaxys

Critical Micelle Concentration (MCS) (2) Temperature Solvent (Critical Comment (Critical References (Critical Micelle Micelle ConcenMicelle ConcenConcentration tration (MCS)) tration (MCS)) (MCS)) [°C] H2O

at:0-40 degreeC.

White et al.; Transactions of the Faraday Society; vol. 54; (1958); p. 1638,1641, View in Reaxys

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H2O

Davies; Griffith; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 6; (1956); p. 143, View in Reaxys

Critical Pressure (1) Critical Pressure References [Torr] 29627.4

Ambrose, D.; Ghiassee, N. B.; Journal of Chemical Thermodynamics; vol. 19; nb. 5; (1987); p. 505 - 520, View in Reaxys

Critical Temperature (3) Critical Tempera- References ture [°C] 345.15

Gude, Michael T.; Mendez-Santiago, Janette; Teja, Amyn S.; Journal of Chemical and Engineering Data; vol. 42; nb. 2; (1997); p. 278 - 280, View in Reaxys

350.85

Ambrose, D.; Ghiassee, N. B.; Journal of Chemical Thermodynamics; vol. 19; nb. 5; (1987); p. 505 - 520, View in Reaxys Kotorlenko; Ukrainskii Khimicheskii Zhurnal (Russian Edition); vol. 28; (1962); p. 333,334, View in Reaxys

Critical Volume (1) References Bhagvanth Rao et al.; Journal of the Indian Institute of Science; vol. 53; (1971); p. 99,103, View in Reaxys Crystal Phase (5) Description (Crys- Comment (Crystal References tal Phase) Phase) Solid state structure properties

Strieter; Templeton; Acta Crystallographica; vol. 15; (1962); p. 1240,1243, View in Reaxys; Baun in Clark; Encyclopedia of X-Rays and Gamma-Rays; (1963); p. 23, View in Reaxys; Gorbunova; Batalin; Russian Journal of Physical Chemistry; vol. 52; (1978); p. 1229; ; p. 2125, View in Reaxys

Association in the solid state

Jakobsen et al.; Spectrochimica Acta; vol. 25A; (1969); p. 839, View in Reaxys

Crystal structure determination

β=111.4 grad, a=8.01 Angstroem, b=6.82 Angstroem, c=10.14 Angstroem, n=4.

Strieter; U.S.Atomic Energy Comm.UCRL-8906; <1959>30, View in Reaxys; Strieter; Templeton; Acta Crystallographica; vol. 15; (1962); p. 1240,1243, View in Reaxys

Crystal structure determination

Strieter; Templeton; Acta Crystallographica; vol. 15; (1962); p. 1240,1243, View in Reaxys

Crystal structure determination

Strieter; Templeton; Acta Crystallographica; vol. 15; (1962); p. 1240,1243, View in Reaxys; Baun; Journal of Physical Chemistry; vol. 65; (1961); p. 2122, View in Reaxys

Crystal Property Description (1) Colour & Other References Properties brown

Rao, Gopal Krishna; Gowda, Narendra B.; Ramakrishna, Ramesha A.; Synthetic Communications; vol. 42; nb. 6; (2012); p. 893 - 904, View in Reaxys

Crystal System (2) Crystal System References monoclinic

Strieter; U.S.Atomic Energy Comm.UCRL-8906; <1959>30, View in Reaxys; Strieter; Templeton; Acta Crystallographica; vol. 15; (1962); p. 1240,1243, View in Reaxys Strieter; Templeton; Acta Crystallographica; vol. 15; (1962); p. 1240,1243, View in Reaxys

Dielectric Constant (8) Dielectric ConFrequency (Diestant lectric Constant) [Hz]

Temperature (Die- References lectric Constant) [°C]

2.85

34.84

1000

Arivazhagan; Shanmugam; Elangovan; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 105; (2013); p. 102 - 108, View in Reaxys

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2.86

1000

29.84

Arivazhagan; Shanmugam; Elangovan; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 105; (2013); p. 102 - 108, View in Reaxys

2.89

1000

39.84

Arivazhagan; Shanmugam; Elangovan; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 105; (2013); p. 102 - 108, View in Reaxys

2.95

1000

44.84

Arivazhagan; Shanmugam; Elangovan; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 105; (2013); p. 102 - 108, View in Reaxys Wollmann; Skaletzki; Schaaf; Die Pharmazie; vol. 29; nb. 10-11; (1974); p. 708 - 711, View in Reaxys; Gerrard; Journal of Applied Chemistry and Biotechnology; vol. 23; (1973); p. 1,8, View in Reaxys; Borowikow; J. Gen. Chem. USSR (Engl. Transl.); vol. 38; (1968); p. 1215,1171, View in Reaxys; Bontchev; Michaylova; Journal of Inorganic and Nuclear Chemistry; vol. 29; (1967); p. 2945,2950, View in Reaxys; Hanson et al.; Journal of Applied Chemistry and Biotechnology; vol. 25; (1975); p. 727,728, View in Reaxys; Niki et al.; Bulletin of the Chemical Society of Japan; vol. 42; (1969); p. 3578, View in Reaxys; Ismailow; Chimenko; Ukrainskii Khimicheskii Zhurnal (Russian Edition); vol. 30; (1964); p. 1266,1267, View in Reaxys; Luzkii; Michailenko; Journal of Structural Chemistry; vol. 4; (1963); p. 12; Zhurnal Strukturnoi Khimii; vol. 4; (1963); p. 14, View in Reaxys; Borovkov; Sov. Prog. Chem. (Engl. Transl.); vol. 35; nb. 4; (1969); p. 358,20, View in Reaxys; Borovikov; Theoretical and Experimental Chemistry; vol. 12; (1976); p. 504; ; p. 648, View in Reaxys

2.98

Piekara; Piekara; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 198; (1934); p. 1020, View in Reaxys

3.04

Piekara; Piekara; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 198; (1934); p. 1020, View in Reaxys

18.5

Dobrosserdow; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 43; (1911); p. 125; Chem. Zentralbl.; vol. 82; nb. I; (1911); p. 955, View in Reaxys

2.83

5E+08

Dissociation Exponent (106) 1 of 106

Dissociation Exponent (pK)

4.82

Dissociation Group

COOH

Type (Dissociation Exponent)

a1/apparent

Location

supporting information

Bühl, Michael; Dabell, Peter; Manley, David W.; McCaughan, Rory P.; Walton, John C.; Journal of the American Chemical Society; vol. 137; nb. 51; (2015); p. 16153 - 16162, View in Reaxys 2 of 106

Dissociation Exponent (pK)

4.82

Type (Dissociation Exponent)

a1/apparent

Location

Paragraph 0021

Patent; Shanghai Techwell Biopharmaceutical Co., Ltd; JIAO, Guangjun; LIU, Shidong; HE, Bingming; TANG, Zhijun; JI, Xiaoming; EP2708533; (2014); (A1) English, View in Reaxys 3 of 106

Dissociation Exponent (pK)

4.81

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

25.04

88/428

2017-08-01 04:43:04

Solvent (Dissociation Exponent)

water

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/thermodynamic

Chen, Yuehua; Wang, Huiyong; Wang, Jianji; Journal of Physical Chemistry B; vol. 118; nb. 17; (2014); p. 4630 4635, View in Reaxys 4 of 106

Dissociation Exponent (pK)

4.82

Type (Dissociation Exponent)

a1/apparent

Location

supporting information

Chen, Jiamei; Lu, Tongbu; Chinese Journal of Chemistry; vol. 31; nb. 5; (2013); p. 635 - 640, View in Reaxys 5 of 106

Dissociation Exponent (pK)

4.821

Temperature (Dissociation Exponent) [°C]

24.84

Solvent (Dissociation Exponent)

water

Type (Dissociation Exponent)

a1/apparent

Location

supporting information

Comment (Dissociation Exponent)

Lomas, John S.; Journal of Physical Organic Chemistry; vol. 25; nb. 8; (2012); p. 620 - 627, View in Reaxys 6 of 106

Dissociation Exponent (pK)

-0.60206

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

water

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/apparent

Comment (Dissociation Exponent)

CONST, DE

Boichenko, Alexander P.; Dung, Le Thi Kim; Loginova, Lidia P.; Journal of Solution Chemistry; vol. 40; nb. 6; (2011); p. 968 - 979, View in Reaxys 7 of 106

Dissociation Exponent (pK)

5.1

Dissociation Group

COOH

Solvent (Dissociation Exponent)

acetonitrile

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/apparent

89/428

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Chechina; Sokolov; Berenblit; Soshin; Russian Journal of Applied Chemistry; vol. 80; nb. 10; (2007); p. 1770 1772, View in Reaxys 8 of 106

Dissociation Exponent (pK)

4.8

Dissociation Group

COOH

Solvent (Dissociation Exponent)

H2O

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/apparent

Chechina; Sokolov; Berenblit; Soshin; Russian Journal of Applied Chemistry; vol. 80; nb. 10; (2007); p. 1770 1772, View in Reaxys 9 of 106

Dissociation Exponent (pK)

4.9

Dissociation Group

COOH

Solvent (Dissociation Exponent)

methanol

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/apparent

Chechina; Sokolov; Berenblit; Soshin; Russian Journal of Applied Chemistry; vol. 80; nb. 10; (2007); p. 1770 1772, View in Reaxys 10 of 106

Dissociation Exponent (pK)

Dissociation Group

COOH

Solvent (Dissociation Exponent)

acetonitrile; H2O

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/apparent

Comment (Dissociation Exponent)

Ratio of solvents: 30percent v/v MeCN

Chechina; Sokolov; Berenblit; Soshin; Russian Journal of Applied Chemistry; vol. 80; nb. 10; (2007); p. 1770 1772, View in Reaxys 11 of 106

Dissociation Exponent (pK)

4.799 - 5.177

Dissociation Group

O-H

Temperature (Dissociation Exponent) [°C]

5 - 120

Solvent (Dissociation Exponent)

H2O

Method (Dissociation Exponent)

calorimetric

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

temperature dependence

McRae; Patterson; Origlia-Luster; Sorenson; Woolley; Journal of Chemical Thermodynamics; vol. 35; nb. 2; (2003); p. 301 - 329, View in Reaxys

90/428

2017-08-01 04:43:04

12 of 106

Dissociation Exponent (pK)

4.87

Dissociation Group

O-H

Type (Dissociation Exponent)

a1/apparent

Pilyugin; Mikhailyuk; Kosareva; Chikisheva; Klimakova; Vorob'eva; Russian Journal of General Chemistry; vol. 73; nb. 9; (2003); p. 1457 - 1462, View in Reaxys 13 of 106

Dissociation Exponent (pK)

4.94 - 5.05

Dissociation Group

Type (Dissociation Exponent)

a1/apparent

Comment (Dissociation Exponent)

in the presence of inorganic compounds

John; Kania; Polish Journal of Chemistry; vol. 75; nb. 6; (2001); p. 905 - 908, View in Reaxys 14 of 106

Dissociation Exponent (pK)

-0.681241

Temperature (Dissociation Exponent) [°C]

Type (Dissociation Exponent)

a1/apparent

Xu, Ning; Vandegrift, Steve; Fine, Dennis D.; Sewell, Guy W.; Environmental Toxicology and Chemistry; vol. 16; nb. 11; (1997); p. 2242 - 2248, View in Reaxys 15 of 106

Dissociation Exponent (pK)

4.79

Dissociation Group

O-H

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

H2O

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/apparent

De Maria; Fontana; Frascari; Gargaro; Spinelli; Tinti; Journal of Pharmaceutical Sciences; vol. 83; nb. 5; (1994); p. 742 - 746, View in Reaxys 16 of 106

Dissociation Exponent (pK)

4.82

Temperature (Dissociation Exponent) [°C]

24.9

Solvent (Dissociation Exponent)

H2O

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/apparent

Headley, Allan D.; Starnes, Stephen D.; Wilson, Leland Y.; Famini, George R.; Journal of Organic Chemistry; vol. 59; nb. 26; (1994); p. 8040 - 8046, View in Reaxys 17 of 106

Dissociation Exponent (pK)

10.1

Temperature (Dissociation Exponent) [°C]

24.9

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Solvent (Dissociation Exponent)

bis-(2-hydroxy-ethyl) ether

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/apparent

Headley, Allan D.; Starnes, Stephen D.; Wilson, Leland Y.; Famini, George R.; Journal of Organic Chemistry; vol. 59; nb. 26; (1994); p. 8040 - 8046, View in Reaxys 18 of 106

Dissociation Exponent (pK)

10.2

Temperature (Dissociation Exponent) [°C]

24.9

Solvent (Dissociation Exponent)

methanol

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/apparent

Headley, Allan D.; Starnes, Stephen D.; Wilson, Leland Y.; Famini, George R.; Journal of Organic Chemistry; vol. 59; nb. 26; (1994); p. 8040 - 8046, View in Reaxys 19 of 106

Dissociation Exponent (pK)

10.2

Temperature (Dissociation Exponent) [°C]

24.9

Solvent (Dissociation Exponent)

1,2-dimethoxy-ethane

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/apparent

Headley, Allan D.; Starnes, Stephen D.; Wilson, Leland Y.; Famini, George R.; Journal of Organic Chemistry; vol. 59; nb. 26; (1994); p. 8040 - 8046, View in Reaxys 20 of 106

Dissociation Exponent (pK)

10.7

Temperature (Dissociation Exponent) [°C]

24.9

Solvent (Dissociation Exponent)

ethanol

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/apparent

Headley, Allan D.; Starnes, Stephen D.; Wilson, Leland Y.; Famini, George R.; Journal of Organic Chemistry; vol. 59; nb. 26; (1994); p. 8040 - 8046, View in Reaxys 21 of 106

Dissociation Exponent (pK)

12.2

Temperature (Dissociation Exponent) [°C]

24.9

Solvent (Dissociation Exponent)

propan-2-ol

Method (Dissociation Exponent)

potentiometric

92/428

2017-08-01 04:43:04

Type (Dissociation Exponent)

a1/apparent

Headley, Allan D.; Starnes, Stephen D.; Wilson, Leland Y.; Famini, George R.; Journal of Organic Chemistry; vol. 59; nb. 26; (1994); p. 8040 - 8046, View in Reaxys 22 of 106

Dissociation Exponent (pK)

15.2

Temperature (Dissociation Exponent) [°C]

29.9

Solvent (Dissociation Exponent)

2-methyl-propan-2-ol

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/apparent

Headley, Allan D.; Starnes, Stephen D.; Wilson, Leland Y.; Famini, George R.; Journal of Organic Chemistry; vol. 59; nb. 26; (1994); p. 8040 - 8046, View in Reaxys 23 of 106

Dissociation Exponent (pK)

339.5

Temperature (Dissociation Exponent) [°C]

24.9

Solvent (Dissociation Exponent)

gas

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/apparent

Headley, Allan D.; Starnes, Stephen D.; Wilson, Leland Y.; Famini, George R.; Journal of Organic Chemistry; vol. 59; nb. 26; (1994); p. 8040 - 8046, View in Reaxys 24 of 106

Dissociation Exponent (pK)

6.35

Dissociation Group

COO-H

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

H2O; dioxane

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 50percent/50percent v/v

John, Ewa; Polish Journal of Chemistry; vol. 64; nb. 1-6; (1990); p. 63 - 67, View in Reaxys 25 of 106

Dissociation Exponent (pK)

4.82

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

ethanol

Type (Dissociation Exponent)

a1/thermodynamic

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Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys 26 of 106

Dissociation Exponent (pK)

5.95

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

ethanol; H2O

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 50:50 (vol.)

Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys 27 of 106

Dissociation Exponent (pK)

6.73

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

ethanol; H2O

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 75:25 (vol.)

Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys 28 of 106

Dissociation Exponent (pK)

7.24

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

ethanol; H2O

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 85:15 (vol.)

Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys 29 of 106

Dissociation Exponent (pK)

5.67

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

2-methyl-propan-2-ol; H2O

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 32:68 (vol.)

94/428

2017-08-01 04:43:04

Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys 30 of 106

Dissociation Exponent (pK)

6.91

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

dimethylsulfoxide; H2O

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 65:35 (vol.)

Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys 31 of 106

Dissociation Exponent (pK)

5.01

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

ethanol; H2O

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 10:90 (vol.)

Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys 32 of 106

Dissociation Exponent (pK)

5.39

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

ethanol; H2O

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 30:70 (vol.)

Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys 33 of 106

Dissociation Exponent (pK)

7.76

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

2-methoxy-ethanol; H2O

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 80:20 (vol.)

95/428

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Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys 34 of 106

Dissociation Exponent (pK)

4.99

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

2-methyl-propan-2-ol; H2O

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 10:90 (vol.)

Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys 35 of 106

Dissociation Exponent (pK)

5.1

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

2-methyl-propan-2-ol; H2O

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 16:84 (vol.)

Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys 36 of 106

Dissociation Exponent (pK)

5.22

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

2-methyl-propan-2-ol; H2O

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 20:80 (vol.)

Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys 37 of 106

Dissociation Exponent (pK)

5.28

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

2-methyl-propan-2-ol; H2O

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 22:78 (vol.)

96/428

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Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys 38 of 106

Dissociation Exponent (pK)

5.42

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

2-methyl-propan-2-ol; H2O

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 26:74 (vol.)

Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys 39 of 106

Dissociation Exponent (pK)

5.58

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

2-methyl-propan-2-ol; H2O

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 30:70 (vol.)

Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys 40 of 106

Dissociation Exponent (pK)

5.92

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

2-methyl-propan-2-ol; H2O

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 40:60 (vol.)

Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys 41 of 106

Dissociation Exponent (pK)

6.24

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

2-methyl-propan-2-ol; H2O

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 50:50 (vol.)

97/428

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Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys 42 of 106

Dissociation Exponent (pK)

6.62

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

2-methyl-propan-2-ol; H2O

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 60:40 (vol.)

Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys 43 of 106

Dissociation Exponent (pK)

7.49

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

2-methyl-propan-2-ol; H2O

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 75:25 (vol.)

Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys 44 of 106

Dissociation Exponent (pK)

9.13

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

2-methyl-propan-2-ol; H2O

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 90:10 (vol.)

Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys 45 of 106

Dissociation Exponent (pK)

5.5 - 5.56

Temperature (Dissociation Exponent) [°C]

-10 - 25

Solvent (Dissociation Exponent)

propan-2-ol; H2O

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/apparent

98/428

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Comment (Dissociation Exponent)

Ratio of solvents: 25 masspercent iPrOH + H2O

Vega, Carmen A.; Rosado, Eliezer; Bates, Roger G.; Journal of Chemical & Engineering Data; vol. 35; (1990); p. 407 - 410, View in Reaxys 46 of 106

Dissociation Exponent (pK)

6.32 - 6.47

Temperature (Dissociation Exponent) [°C]

-10 - 25

Solvent (Dissociation Exponent)

propan-2-ol; H2O

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/apparent

Comment (Dissociation Exponent)

Ratio of solvents: 50 masspercent iPrOH + H2O

Vega, Carmen A.; Rosado, Eliezer; Bates, Roger G.; Journal of Chemical & Engineering Data; vol. 35; (1990); p. 407 - 410, View in Reaxys 47 of 106

Dissociation Exponent (pK)

-0.68

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

H2O

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/apparent

Fini; De Maria; Guarnieri; Varoli; Journal of Pharmaceutical Sciences; vol. 76; nb. 1; (1987); p. 48 - 52, View in Reaxys 48 of 106

Dissociation Exponent (pK)

-0.93

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

dimethylsulfoxide; H2O

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/apparent

Comment (Dissociation Exponent)

Ratio of solvents: 80percent w/w

Fini; De Maria; Guarnieri; Varoli; Journal of Pharmaceutical Sciences; vol. 76; nb. 1; (1987); p. 48 - 52, View in Reaxys 49 of 106

Dissociation Exponent (pK)

4.78

Dissociation Group

-COOH

Temperature (Dissociation Exponent) [°C]

99/428

2017-08-01 04:43:04

Solvent (Dissociation Exponent)

H2O

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/apparent

Vanin; Krut-skii; Sveshnikova; Krut-skaya; Journal of applied chemistry of the USSR; vol. 57; nb. 3 pt 2; (1984); p. 577 - 579, View in Reaxys 50 of 106

Dissociation Exponent (pK)

8.56

Dissociation Group

COO-H

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

dimethylsulfoxide; H2O

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/thermodynamic

Comment (Dissociation Exponent)

Ratio of solvents: 80:20

De Maria; Fini; Guarnieri; Varoli; Archiv der Pharmazie; vol. 316; nb. 6; (1983); p. 559 - 563, View in Reaxys 51 of 106

Dissociation Exponent (pK)

4.82

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Type (Dissociation Exponent)

a1/apparent

Kawabata; Higuchi; Yoshida; Bulletin of the Chemical Society of Japan; vol. 54; nb. 11; (1981); p. 3253 - 3258, View in Reaxys 52 of 106

Dissociation Exponent (pK)

4.77

Dissociation Group

H(+)

Temperature (Dissociation Exponent) [°C]

Type (Dissociation Exponent)

a1/apparent

Kiso, Yoshiyuki; Hirokawa, Takeshi; Chemistry Letters; (1980); p. 323 - 326, View in Reaxys 53 of 106

Dissociation Exponent (pK)

5.05

Dissociation Group

COOH

Temperature (Dissociation Exponent) [°C]

Type (Dissociation Exponent)

a1/apparent

John, Ewa; Polish Journal of Chemistry; vol. 54; nb. 11/12; (1980); p. 2351 - 2356, View in Reaxys 54 of 106

Comment (Dissociation Exponent)

(pk')pK(a)

Yalkowsky; Zografi; Journal of pharmaceutical sciences; vol. 59; nb. 6; (1970); p. 798 - 802, View in Reaxys; Abe; Ito; Bulletin of the Chemical Society of Japan; vol. 52; (1979); p. 261, View in Reaxys

100/428

2017-08-01 04:43:04

55 of 106

Comment (Dissociation Exponent)

(pk')Anion 3b: pK(A)

van de Langkruis; Engberts; Journal of Organic Chemistry; vol. 44; (1979); p. 141, View in Reaxys 56 of 106

Comment (Dissociation Exponent)

(pk')

Dash; Thermochimica Acta; vol. 32; (1979); p. 33,34, View in Reaxys 57 of 106

Comment (Dissociation Exponent)

(pk')pK

Dash; Thermochimica Acta; vol. 27; (1978); p. 379,380, 381, View in Reaxys; Izmailov et al.; Russian Journal of Physical Chemistry; vol. 37; (1963); p. 427; Zhurnal Fizicheskoi Khimii; vol. 37; (1963); p. 822, View in Reaxys; Yoshizawa; Inukai; Bulletin of the Chemical Society of Japan; vol. 42; (1969); p. 3238,3240, View in Reaxys 58 of 106

Comment (Dissociation Exponent)

(k')Rk. mit H2O2

Shapilov; Kinetics and Catalysis; vol. 17; (1976); p. 687, View in Reaxys 59 of 106

Comment (Dissociation Exponent)

(pk')pK(S) in Acetonitril

Chantooni; Kolthoff; Journal of Physical Chemistry; vol. 79; (1975); p. 1176,1177, 1181, View in Reaxys 60 of 106

Comment (Dissociation Exponent)

(pk')pK in H2O-tert-BuOH-Gemischen; S. 406

Morel et al.; Journal of Solution Chemistry; vol. 3; (1974); p. 403, View in Reaxys 61 of 106

Comment (Dissociation Exponent)

(pk')pK(a) (Tab.1)

Blinova,G.G. et al.; Zhurnal Organicheskoi Khimii; vol. 10; nb. 10; (1974); p. 2089 - 2093,2105 - 2108, View in Reaxys 62 of 106

Comment (Dissociation Exponent)

(k')Fig. 1; Δ v (Tab. VII)

Suzuki et al.; Journal of Physical Chemistry; vol. 77; (1973); p. 1918, View in Reaxys 63 of 106

Comment (Dissociation Exponent)

(pk')pK-Wert (Tab. III, S. 5809)

Storm,D.R.; Koshland,D.E.; Journal of the American Chemical Society; vol. 94; (1972); p. 5805 - 5814, View in Reaxys 64 of 106

Comment (Dissociation Exponent)

(pk')pK (S. 565)

Trautmann; Schoellner; Journal fuer Praktische Chemie (Leipzig); vol. 313; (1971); p. 561, View in Reaxys 65 of 106

Comment (Dissociation Exponent)

(pk')pK(a): 5.13 (20percentig. A., potentiometrisch ermittelt) (Tab. 2)

Deles; Szechner; Roczniki Chemii; vol. 45; (1971); p. 1243,1245, 1247, View in Reaxys 66 of 106

Comment (Dissociation Exponent)

(pk')pKa(Tab.1)

Tarasyants,R.R. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 41; (1971); p. 136 - 139,131 - 133, View in Reaxys 67 of 106

Comment (Dissociation Exponent)

(pk')pK(react) (Anal. von pK(a)) in Anisol, Butylether, Butylacetat

Gureeva; Dulova; Russian Journal of Physical Chemistry; vol. 45; (1971); p. 257; ; p. 461, View in Reaxys 68 of 106

Comment (Dissociation Exponent)

(pk')pK(a)-Wert

Church; Weiss; Journal of Organic Chemistry; vol. 35; (1970); p. 2465, View in Reaxys 69 of 106

Comment (Dissociation Exponent)

(pk')pK = 4.83

Yalkowsky; Zografi; Journal of pharmaceutical sciences; vol. 59; nb. 6; (1970); p. 798 - 802, View in Reaxys

101/428

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70 of 106

Comment (Dissociation Exponent)

(k')Saeurekonst.

Kojima et al.; Journal of Inorganic and Nuclear Chemistry; vol. 32; (1970); p. 987,989, View in Reaxys 71 of 106

Comment (Dissociation Exponent)

(k')

Yagi et al.; Journal of Biochemistry (Tokyo, Japan); vol. 68; (1970); p. 293,295, View in Reaxys 72 of 106

Comment (Dissociation Exponent)

(pk')pK(a): 9.4 (Me.), 10.0 (DMF), 11.0 (DMSO)

Butin et al.; Journal of Organometallic Chemistry; vol. 20; (1969); p. 11,13, View in Reaxys 73 of 106

Comment (Dissociation Exponent)

(pk')pK-Wert ( Variat. d. Lsgm.)

Reynaud; Bulletin de la Societe Chimique de France; (1969); p. 699, View in Reaxys 74 of 106

Comment (Dissociation Exponent)

(pk')pK(a) (80percentig. 2-Methoxy-aethanol/W.)

Bowden et al.; Canadian Journal of Chemistry; vol. 46; (1968); p. 2929,2930, View in Reaxys 75 of 106

Comment (Dissociation Exponent)

(pk')Korrelat. d. pK-Werte in wss. -organ. Lsgm.

Reynaud; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 267; (1968); p. 989, View in Reaxys 76 of 106

Comment (Dissociation Exponent)

(pk')pK(a)-Wert ( abs. Me. )

Moreau; Bulletin de la Societe Chimique de France; (1968); p. 31, View in Reaxys 77 of 106

Comment (Dissociation Exponent)

(pk')pK(a) und pK' (Wasser bzw. n-Bu4NBr-Lsg., potentiometrisch ermittelt) bei 25grad: 4.82 bzw. 7.18

Steigman; Sussman; Journal of the American Chemical Society; vol. 89; (1967); p. 6400,6403, View in Reaxys 78 of 106

Comment (Dissociation Exponent)

(pk')pK = 4,81 ( weitere pK-Mess. in Me.-W.-Gemischen )

Alfenaar; de Ligny; Recueil des Travaux Chimiques des Pays-Bas; vol. 86; (1967); p. 952, View in Reaxys 79 of 106

Comment (Dissociation Exponent)

(pk')pKa (pot.best.; MeOH; Wasser)

Juillard; Bulletin de la Societe Chimique de France; (1966); p. 1727,1729, View in Reaxys 80 of 106

Comment (Dissociation Exponent)

(k')dimere Saeure in o-Dichlorbenzol (IR-spektroskopisch ermittelt) bei 28grad

Satchell; Wardell; Transactions of the Faraday Society; vol. 61; (1965); p. 1199, View in Reaxys 81 of 106

Comment (Dissociation Exponent)

(k')1.54*10-5

Kozlov,V.V.; Belov,B.I.; J. Gen. Chem. USSR (Engl. Transl.); vol. 33; (1963); p. 1951 - 1955,1898 - 1901, View in Reaxys 82 of 106

Comment (Dissociation Exponent)

(k')Ionisationskonst. in W., Me., A., wss. Me., wss. A. und in wss. Dioxan

Dondon; Paris; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 58; (1961); p. 222,223, View in Reaxys 83 of 106

Comment (Dissociation Exponent)

(pk')pK (ref. 5)

Bystrov et al.; Optics and Spectroscopy; vol. 10; (1961); p. 68; ; p. 138, View in Reaxys 84 of 106

Dissociation Exponent (pK)

4.82

Temperature (Dissociation Exponent) [°C]

102/428

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Solvent (Dissociation Exponent)

H2O

Method (Dissociation Exponent)

conductometric

Type (Dissociation Exponent)

a/thermodynamic

Cartwright; Monk; Journal of the Chemical Society; (1955); p. 2500, View in Reaxys 85 of 106

Dissociation Exponent (pK)

4.8

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

H2O

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a/thermodynamic

Everett et al.; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 215; (1952); p. 403,409, View in Reaxys 86 of 106

Dissociation Exponent (pK)

4.92

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

H2O

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a/thermodynamic

Everett et al.; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 215; (1952); p. 403,409, View in Reaxys 87 of 106

Dissociation Exponent (pK)

4.82

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

H2O

Method (Dissociation Exponent)

conductometric

Type (Dissociation Exponent)

apparent

Belcher; Journal of the American Chemical Society; vol. 60; (1938); p. 2745, View in Reaxys; Saxton; Darken; Journal of the American Chemical Society; vol. 62; (1940); p. 852, View in Reaxys; Dippy; Journal of the Chemical Society; (1938); p. 1226,1227, View in Reaxys 88 of 106

Dissociation Exponent (pK)

4.81

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

H2O

Method (Dissociation Exponent)

potentiometric

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Type (Dissociation Exponent)

apparent

Harned; Sutherland; Journal of the American Chemical Society; vol. 56; (1934); p. 2039, View in Reaxys 89 of 106

Dissociation Exponent (pK)

4.82

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

H2O

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

apparent

Harned; Sutherland; Journal of the American Chemical Society; vol. 56; (1934); p. 2039, View in Reaxys 90 of 106

Dissociation Exponent (pK)

4.92

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

H2O

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

apparent

Harned; Sutherland; Journal of the American Chemical Society; vol. 56; (1934); p. 2039, View in Reaxys 91 of 106

Dissociation Exponent (pK)

7.24

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

methanol

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a/apparent

Bright; Briscoe; Journal of Physical Chemistry; vol. 37; (1933); p. 787,789, View in Reaxys 92 of 106

Dissociation Exponent (pK)

7.9

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

ethanol

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a/apparent

Bright; Briscoe; Journal of Physical Chemistry; vol. 37; (1933); p. 787,789, View in Reaxys 93 of 106

Dissociation Exponent (pK)

4.82

Temperature (Dissociation Exponent) [°C]

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Solvent (Dissociation Exponent)

H2O

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

apparent

Larsson; Adell; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 156; (1931); p. 391, View in Reaxys 94 of 106

Temperature (Dissociation Exponent) [°C]

19.3

Solvent (Dissociation Exponent)

H2O; ethanol

Method (Dissociation Exponent)

potentiometric

Mizutani; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 118; (1925); p. 329, View in Reaxys 95 of 106

Solvent (Dissociation Exponent)

H2O; methanol

Method (Dissociation Exponent)

potentiometric

Comment (Dissociation Exponent)

at:19-19.5 degreeC.

Mizutani; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 118; (1925); p. 329, View in Reaxys 96 of 106

Dissociation Exponent (pK)

4.8

Temperature (Dissociation Exponent) [°C]

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

apparent

Landolt-Boernst. E I 651, View in Reaxys; Mizutani; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 116; (1925); p. 351; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 118; (1925); p. 328,341, View in Reaxys 97 of 106

Dissociation Exponent (pK)

4.8

Temperature (Dissociation Exponent) [°C]

19.3

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

apparent

Dissociation Exponent (pK)

4.81

Temperature (Dissociation Exponent) [°C]

Type (Dissociation Exponent)

apparent

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Billitzer; Monatshefte fuer Chemie; vol. 20; (1899); p. 676, View in Reaxys; Klein; Lotos; vol. 71; (1923); p. 280, View in Reaxys 99 of 106

Dissociation Exponent (pK)

4.83

Temperature (Dissociation Exponent) [°C]

Type (Dissociation Exponent)

apparent

Ostwald; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 3; (1889); p. 190, View in Reaxys; Verkade; Recueil des Travaux Chimiques des Pays-Bas; vol. 35; (1916); p. 102, View in Reaxys; Holwerda; Biochemische Zeitschrift; vol. 128; (1922); p. 468, View in Reaxys 100 of 106 Dissociation Exponent (pK)

4.81

Temperature (Dissociation Exponent) [°C]

Type (Dissociation Exponent)

apparent

Verkade; Recueil des Travaux Chimiques des Pays-Bas; vol. 35; (1916); p. 102, View in Reaxys 101 of 106 Dissociation Exponent (pK)

4.85

Temperature (Dissociation Exponent) [°C]

Type (Dissociation Exponent)

apparent

Wilsdon; Sidgwick; Journal of the Chemical Society; vol. 103; (1913); p. 1965, View in Reaxys 102 of 106 Dissociation Exponent (pK)

4.82

Temperature (Dissociation Exponent) [°C]

Type (Dissociation Exponent)

apparent

White; Jones; American Chemical Journal; vol. 44; (1910); p. 197, View in Reaxys; Franke; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 16; (1895); p. 483, View in Reaxys 103 of 106 Dissociation Exponent (pK)

4.79

Temperature (Dissociation Exponent) [°C]

Type (Dissociation Exponent)

apparent

White; Jones; American Chemical Journal; vol. 44; (1910); p. 197, View in Reaxys 104 of 106 Dissociation Exponent (pK)

4.84

Temperature (Dissociation Exponent) [°C]

Type (Dissociation Exponent)

apparent

Bauer; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 56; (1906); p. 219, View in Reaxys 105 of 106 Dissociation Exponent (pK) Temperature (Dissociation Exponent) [°C]

4.76 25

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Type (Dissociation Exponent)

apparent

Drucker; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 52; (1905); p. 649, View in Reaxys 106 of 106 Dissociation Exponent (pK)

4.78

Temperature (Dissociation Exponent) [°C]

Type (Dissociation Exponent)

apparent

Kortright; American Chemical Journal; vol. 18; (1896); p. 369, View in Reaxys Dynamic Viscosity (14) Dynamic Viscosi- Temperature (Dyty [P] namic Viscosity) [°C]

Comment (Dynamic Viscosity)

References

0.009562

44.99

Liquid

Ahluwalia; Gupta, Ritu; Vashisht; Wanchoo; Journal of Solution Chemistry; vol. 42; nb. 5; (2013); p. 945 - 966, View in Reaxys

0.012421

34.99

Liquid

Ahluwalia; Gupta, Ritu; Vashisht; Wanchoo; Journal of Solution Chemistry; vol. 42; nb. 5; (2013); p. 945 - 966, View in Reaxys

0.015283

24.99

Liquid

Ahluwalia; Gupta, Ritu; Vashisht; Wanchoo; Journal of Solution Chemistry; vol. 42; nb. 5; (2013); p. 945 - 966, View in Reaxys

0.01396

Roy, Mahendra Nath; Sinha, Biswajit; Dakua, Vikas Kumar; Journal of Chemical and Engineering Data; vol. 51; nb. 2; (2006); p. 590 594, View in Reaxys

0.01405

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

Sen; Indian Journal of Physics (1926-1976); vol. 25; (1951); p. 237,241, View in Reaxys

0.0154

Staudinger; Bauer; Helvetica Chimica Acta; vol. 16; (1933); p. 422,425, View in Reaxys

0.0112

Staudinger; Bauer; Helvetica Chimica Acta; vol. 16; (1933); p. 422,425, View in Reaxys

0.00857

Staudinger; Bauer; Helvetica Chimica Acta; vol. 16; (1933); p. 422,425, View in Reaxys

0.01814

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys

0.01385

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys

0.006045 0.01538

20 - 90

Dunstan; Journal of the Chemical Society; vol. 107; (1915); p. 668, View in Reaxys

0.01554

Merry; Turner; Journal of the Chemical Society; vol. 105; (1914); p. 758, View in Reaxys

0.01227

Merry; Turner; Journal of the Chemical Society; vol. 105; (1914); p. 758, View in Reaxys

Electrical Data (18) 1 of 18

Description (Electrical Data)

Electrical conductivity

Ellis; Journal of the Chemical Society; (1963); p. 2299,2302, View in Reaxys; Ssumarokowa; Nurmakowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 29,29; Chem.Abstr.; nb. 19134; (1960), View in Reaxys; Deryagin et al.; Doklady Physical Chemistry; vol. 208-213; (1973); p. 1070, View in Reaxys; Makni; Piekarski; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 270; (1970); p. 1348, View in Reaxys; Hoeiland; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 70; (1974); p. 1180, View in Reaxys; Hoeiland; Acta Chemica Scandinavica (1947-1973); vol. 27; (1973); p. 2687,2689,2691, View in Reaxys; Huang, Xiaohua; Zare, Richard N.; Sloss, Sandra; Ewing, Andrew G.; Analytical Chemistry; vol. 63; nb. 2; (1991); p. 189 - 192, View in Reaxys; Khar'kin, V. S.; Lyashchenko,

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A. K.; Russian Journal of Physical Chemistry; vol. 66; nb. 8; (1992); p. 1201 - 1204; Zhurnal Fizicheskoi Khimii; vol. 66; (1992); p. 2250 - 2255, View in Reaxys 2 of 18

Description (Electrical Data)

Dielectric relaxation time

Khar'kin, V. S.; Lyashchenko, A. K.; Russian Journal of Physical Chemistry; vol. 66; nb. 8; (1992); p. 1201 - 1204; Zhurnal Fizicheskoi Khimii; vol. 66; (1992); p. 2250 - 2255, View in Reaxys; Kaatze; Woermann; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 86; nb. 1; (1982); p. 81 - 87, View in Reaxys 3 of 18

Description (Electrical Data)

Cole-Cole diagram

Kaatze; Woermann; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 86; nb. 1; (1982); p. 81 - 87, View in Reaxys 4 of 18

Description (Electrical Data)

Electrical properties

Deryagin et al.; Doklady Physical Chemistry; vol. 208-213; (1973); p. 1070, View in Reaxys 5 of 18

Description (Electrical Data)

Dielectric increment

Comment (Electrical Da- in Aethanol, in 2-Methoxy-aethanol und in Aceton. ta) Hoigne; Gaeumann; Helvetica Chimica Acta; vol. 41; (1958); p. 1933,1949, View in Reaxys 6 of 18

Description (Electrical Data)

Dielectric loss

Comment (Electrical Da- bei Temperaturen 67.5grad bis 120grad und Frequenzen von 250 MHz bis 510 MHz. ta) Sen; Indian Journal of Physics (1926-1976); vol. 25; (1951); p. 237,241, View in Reaxys 7 of 18

Description (Electrical Data)

Electrical conductivity

Comment (Electrical Da- von Gemischen mit Aceton. ta) Rebek; Mandrino; Collection of Czechoslovak Chemical Communications; vol. 5; (1933); p. 325, View in Reaxys 8 of 18

Description (Electrical Data)

Electrical conductivity

Comment (Electrical Da- von Gemischen mit Ameisensaeure. ta) Fulmer; Moore; Foster; Journal of Physical Chemistry; vol. 35; (1931); p. 1228, View in Reaxys 9 of 18

Description (Electrical Data)

Electrical conductivity

Comment (Electrical Da- von verduennten und konz.wss.Loesungen bei 0grad und 25grad. ta) Grindley; Bury; Journal of the Chemical Society; (1930); p. 1665, View in Reaxys 10 of 18

Description (Electrical Data)

Electrical conductivity

Comment (Electrical Da- waessr.Loesungen bei 0grad und 25grad. ta) Verkade; Recueil des Travaux Chimiques des Pays-Bas; vol. 35; (1916); p. 102, View in Reaxys 11 of 18

Description (Electrical Data)

Electrical conductivity

Comment (Electrical Da- waessr.Loesungen bei 25grad. ta) Wilsdon; Sidgwick; Journal of the Chemical Society; vol. 103; (1913); p. 1965, View in Reaxys 12 of 18

Description (Electrical Data)

Electrical conductivity

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Comment (Electrical Da- in fluessigem Bromwasserstoff und fluessigem Chlorwasserstoff. ta) Archibald; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 11; (1913); p. 765, View in Reaxys 13 of 18

Description (Electrical Data)

Electrical conductivity

Comment (Electrical Da- waessr.Loesungen bei 0grad und 65grad. ta) White; Jones; American Chemical Journal; vol. 44; (1910); p. 182, View in Reaxys; Smith; Jones; American Chemical Journal; vol. 50; (1913); p. 22, View in Reaxys 14 of 18

Description (Electrical Data)

Electrical conductivity

Comment (Electrical Da- bei Verduennungen von n/2 bis n/2048 und Temperaturen zwischen 0gradund 35grad. ta) White; Jones; American Chemical Journal; vol. 42; (1909); p. 529, View in Reaxys 15 of 18

Description (Electrical Data)

Electrical conductivity

Comment (Electrical Da- in verfluessigtem Chlorwasserstoff und Bromwasserstoff. ta) Archibald; Journal of the American Chemical Society; vol. 29; (1907); p. 1421, View in Reaxys 16 of 18

Description (Electrical Data)

Electrical conductivity

Comment (Electrical Da- unvollstaendig neutralisierter Buttersaeure-Loesungen. ta) Barmwater; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 56; (1906); p. 230, View in Reaxys 17 of 18

Description (Electrical Data)

Electrical conductivity

Comment (Electrical Da- des Lithium-,Natrium-und Kaliumsalzes. ta) Ostwald; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 1; (1887); p. 100,103,104; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 3; (1889); p. 175, View in Reaxys 18 of 18

Description (Electrical Data)

Electrical conductivity

Comment (Electrical Da- des Magnesiumsalzes. ta) Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 1; (1887); p. 532, View in Reaxys Electrical Moment (7) 1 of 7

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

Wollmann; Skaletzki; Schaaf; Die Pharmazie; vol. 29; nb. 10-11; (1974); p. 708 - 711, View in Reaxys; Hanson et al.; Journal of Applied Chemistry and Biotechnology; vol. 25; (1975); p. 727,728, View in Reaxys 2 of 7

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

μ(B), μ(Liq)

Meyyappan; Aranachalam; Journal of the Indian Chemical Society; vol. 49; (1972); p. 1047, View in Reaxys 3 of 7

Description (Electrical Moment)

Dipole moment

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Comment (Electrical Moment)

reine Substanz

Kovrigina; Bogdanov; Russian Journal of Physical Chemistry; vol. 44; (1970); p. 881; ; p. 1571, View in Reaxys 4 of 7

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

S. 1328

Le Fevre et al.; Australian Journal of Chemistry; vol. 19; (1966); p. 1325, View in Reaxys 5 of 7

Description (Electrical Moment)

Dipole moment

Temperature (Electrical Moment) [°C]

25 - 120

Method (Electrical Moment)

Dielectric constant (ε)

Solvent (Electrical Moment)

neat (no solvent)

Phadke; Journal of the Indian Institute of Science, Section A; vol. 34; (1952); p. 189,199, View in Reaxys 6 of 7

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.58

Method (Electrical Moment)

Dielectric constant (ε)

Solvent (Electrical Moment)

dioxane

Potapenko; Wheeler; Rev.mod.Physics; vol. 20; (1948); p. 149, View in Reaxys 7 of 7

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.65

Method (Electrical Moment)

Dielectric constant (ε)

Solvent (Electrical Moment)

benzene

Pohl; Hobbs; Gross; Journal of Chemical Physics; vol. 9; (1941); p. 413, View in Reaxys; Wolf; Phys.Z.; vol. 31; (1930); p. 228, View in Reaxys; Briegleb; Zeitschrift fuer Physikalische Chemie, Abteilung B: Chemie der Elementarprozesse, Aufbau der Materie; vol. 10; (1930); p. 220, View in Reaxys Electrical Polarizability (2) Description (Elec- References trical Polarizability) Molar polarization Miller; Savchik; Journal of the American Chemical Society; vol. 101; (1979); p. 7206,7210, View in Reaxys Optical anisotropy Luong The Man et al.; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 260; (1965); p. 2755 - 2758, View in Reaxys Electrochemical Behaviour (28) Description (Elec- Comment (Electrochemical Betrochemical Behaviour) haviour)

References

Enthalpy of disso- in the presence of Sukhno; Arutyunyan; Buz'ko; Klimova; Russian Journal of Physical Chemistry A; vol. ciation (electrolyt- salts 78; nb. 7; (2004); p. 1091 - 1093, View in Reaxys ic) / protonation Electrolytic dissociation / protonation equilibrium

temperature dependence. Ob-

Sue, Kiwamu; Ouchi, Fumiaki; Minami, Kimitaka; Arai, Kunio; Journal of Chemical and Engineering Data; vol. 49; nb. 5; (2004); p. 1359 - 1363, View in Reaxys

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ject(s) of Study: high pressure Thermodynamic parameters for dissociation / protonation

temperature dependence

McRae; Patterson; Origlia-Luster; Sorenson; Woolley; Journal of Chemical Thermodynamics; vol. 35; nb. 2; (2003); p. 301 - 329, View in Reaxys

Thermodynamic parameters for dissociation / protonation

Vega, Carmen A.; Rosado, Eliezer; Bates, Roger G.; Journal of Chemical & Engineering Data; vol. 35; (1990); p. 407 - 410, View in Reaxys; Caldwell, Gary; Renneboog, Richard; Kebarle, Paul; Canadian Journal of Chemistry; vol. 67; (1989); p. 611 - 618, View in Reaxys; Butler, James J.; Fraser-Monteiro, Maria L.; Fraser-Monteiro, Luis; Baer, Tomas; Hass, J. Ronald; Journal of Physical Chemistry; vol. 86; nb. 5; (1982); p. 747 - 752, View in Reaxys; Headley, Allan D.; McMurry, Mike E.; Starnes, Stephen D.; Journal of Organic Chemistry; vol. 59; nb. 7; (1994); p. 1863 - 1866, View in Reaxys; Panyushkin; Storozhenko; Sukhno; Arutyunyan; Russian Journal of General Chemistry; vol. 72; nb. 8; (2002); p. 1170 - 1172, View in Reaxys

Enthalpy of dissociation (electrolytic) / protonation

Panyushkin; Storozhenko; Sukhno; Arutyunyan; Russian Journal of General Chemistry; vol. 72; nb. 8; (2002); p. 1170 - 1172, View in Reaxys

Enthalpy of neutralization

Panyushkin; Storozhenko; Sukhno; Arutyunyan; Russian Journal of General Chemistry; vol. 72; nb. 8; (2002); p. 1170 - 1172, View in Reaxys

Thermodynamic parameters for dissociation / protonation

in the presence of John; Kania; Polish Journal of Chemistry; vol. 75; nb. 6; (2001); p. 905 - 908, inorganic comView in Reaxys pounds

Electrolytic dissociation / protonation equilibrium

Nuernberg et al.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 52; (1967); p. 144, View in Reaxys; Christensen; Izatt; Journal of Physical Chemistry; vol. 66; (1962); p. 1030,1032, View in Reaxys; Christensen et al.; Journal of the American Chemical Society; vol. 92; (1970); p. 4164, View in Reaxys; Hoefnagel, A. J.; Wepster, B. M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 109; nb. 9; (1990); p. 455 462, View in Reaxys; De Maria; Fontana; Frascari; Gargaro; Spinelli; Tinti; Journal of Pharmaceutical Sciences; vol. 83; nb. 5; (1994); p. 742 - 746, View in Reaxys; Mukerjee, Pasupati; Ostrow, J. Donald; Tetrahedron Letters; vol. 39; nb. 5-6; (1998); p. 423 - 426, View in Reaxys

Proton affinity

Borchers; Levsen; International Journal of Mass Spectrometry and Ion Physics; vol. 31; (1979); p. 247,255, View in Reaxys; McLuckey, S. A.; Cameron, D.; Cooks, R. G.; Journal of the American Chemical Society; vol. 103; nb. 6; (1981); p. 1313 - 1317, View in Reaxys

Electrochemical properties

Mueller; Lorenz; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 27; (1961); p. 23, View in Reaxys; Grilikhes et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 48; (1975); p. 442,447, View in Reaxys; Chifu; Albu; Revista de Chimie (Bucharest, Romania); vol. 30; (1979); p. 1004, View in Reaxys

Acidity

Cumming; Kebarle; Canadian Journal of Chemistry; vol. 56; (1978); p. 1,5, View in Reaxys; Yamadagni; Kebarle; Journal of the American Chemical Society; vol. 95; (1973); p. 4050,4051, View in Reaxys

Enthalpy of disso- . ciation (electrolytic) / protonation

Morel et al.; Journal of Solution Chemistry; vol. 3; (1974); p. 403, View in Reaxys

Kinetics of dissociation (electrolytic) / protonation

Michels; Zana; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 66; (1969); p. 240, View in Reaxys

Volume change on dissociation

Michels; Zana; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 66; (1969); p. 240, View in Reaxys

Basicity

Wells; Transactions of the Faraday Society; vol. 63; (1967); p. 147,151, View in Reaxys

Polarography

Fioschin; Wasilew; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1963); p. 393; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1963); p. 437, View in Reaxys

Enthalpy of disso- Temperature: 25 ciation (electrolyt- deg C.; in Wassic) / protonation er.

Canady et al.; Transactions of the Faraday Society; vol. 54; (1958); p. 502, View in Reaxys; Everett et al.; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 215; (1952); p. 403,409, View in Reaxys

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Enthalpy of neutralization

in Wasser bei 25grad.

Canady et al.; Transactions of the Faraday Society; vol. 54; (1958); p. 502, View in Reaxys

Electrolytic dissociation / protonation equilibrium

in Wasser-Methanol-Gemischen bei 25grad.

Bacarella et al.; Journal of Organic Chemistry; vol. 20; (1955); p. 747,752, View in Reaxys

Autoprotolysis

Enthalpie, Entro- Harris; Alder; Transactions of the Faraday Society; vol. 50; (1954); p. 13,15, pie und Gibbs-En- View in Reaxys ergie der Autoprotolyse (Dissoziation in 1,1-Dihydroxy-butylium und Butyrat) von binaer assoziierter Buttersaeure bei 25-120grad.

Electrolytic dissociation / protonation equilibrium

in Wasser-Aethanol-Gemischen bei 25grad.

Grunwald; Berkowitz; Journal of the American Chemical Society; vol. 73; (1951); p. 4939,4942, View in Reaxys

Enthalpy of disso- .; bei 10, 20 und ciation (electrolyt- 30grad. ic) / protonation

Cottrell et al.; Journal of the Chemical Society; (1948); p. 1017,1018, View in Reaxys

Electrolytic dissociation / protonation equilibrium

Dissoziation in IsopropylalkoholWasser-Gemischen bei 0-40grad:.

Felsing; May; Journal of the American Chemical Society; vol. 70; (1948); p. 2904, View in Reaxys

Electrolytic dissociation / protonation equilibrium

Potentiometrische Cannan; Kibrick; Journal of the American Chemical Society; vol. 60; (1938); p. 2317, Untersuchung der View in Reaxys Dissoziation in wss.Loesungen von KCl,KCl +ZnCl2 und KCl +MgCl2.

Electrolytic dissociation / protonation equilibrium

Dissoziation in Di- Lynch; La Mer; Journal of the American Chemical Society; vol. 60; (1938); p. oxan-Wasser1252,1257, 1259, View in Reaxys Gemischen:.

Electrolytic dissociation / protonation equilibrium

in Butylalkohol.

Electrolytic dissociation / protonation equilibrium

Dissoziation in Jukes; Schmidt; Journal of Biological Chemistry; vol. 110; (1935); p. 10, View in Reaxys Aethanol-WasserGemischen:.

Electrolytic dissociation / protonation equilibrium

Potentiometrische Larsson; Adell; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische ThermoUntersuchung der dynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 156; (1931); p. 391, Dissoziation in View in Reaxys wss.Loesungen von NaCl und KCl.

Wooten; Hammett; Journal of the American Chemical Society; vol. 57; (1935); p. 2289,2293, View in Reaxys

Electrochemical Characteristics (2) 1 of 2

Description (Electrochemical Characteristics)

polarographic half-wave potential

Tarasyants,R.R. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 41; (1971); p. 136 - 139,131 - 133, View in Reaxys 2 of 2

Description (Electrochemical Characteristics)

polarographic current/voltage curve

Comment (Electrochem- in Wasser und in wss.Aceton. ical Characteristics) Maruta; Iwama; Nippon Kagaku Zasshi; vol. 76; (1955); p. 548; Chem.Abstr.; (1956); p. 11135, View in Reaxys; Asahara et al.; Kogyo Kagaku Zasshi; vol. 60; (1957); p. 178,182; Chem.Abstr.; (1959); p. 2885, View in Reaxys

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Electron Binding (1) Description (Elec- References tron Binding) Electron affinity

Caldwell, Gary; Renneboog, Richard; Kebarle, Paul; Canadian Journal of Chemistry; vol. 67; (1989); p. 611 - 618, View in Reaxys

Energy Data (MCS) (32) 1 of 32

Description (Energy Data (MCS))

Molar excess Gibbs free energy

Temperature (Energy Data (MCS)) [°C]

Pressure (Energy Data (MCS)) [Torr]

760

Comment (Energy Data (MCS))

gas

Partner (Energy Data (MCS))

cetane

Jamalizadeh; Hosseini; Russian Journal of Physical Chemistry A; vol. 80; nb. 9; (2006); p. 1423 - 1427, View in Reaxys 2 of 32

Description (Energy Data (MCS))

Enthalpy of mixing

Solvent (Energy Data (MCS))

H2O

Temperature (Energy Data (MCS)) [°C]

24.85

Partner (Energy Data (MCS))

MgCl2

Arutyunyan; Panyushkin; Russian Journal of Physical Chemistry A; vol. 78; nb. 7; (2004); p. 1173 - 1174, View in Reaxys 3 of 32

Description (Energy Data (MCS))

Heat capacity Cp

Temperature (Energy Data (MCS)) [°C]

5 - 120

Pressure (Energy Data (MCS)) [Torr]

2625.21

Comment (Energy Data (MCS))

concentration dependence. Object(s) of Study: temperature dependence

Partner (Energy Data (MCS))

H2O

McRae; Patterson; Origlia-Luster; Sorenson; Woolley; Journal of Chemical Thermodynamics; vol. 35; nb. 2; (2003); p. 301 - 329, View in Reaxys 4 of 32

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Comment (Energy Data (MCS))

concentration dependence. Object(s) of Study: diagram

Partner (Energy Data (MCS))

propyl cyanide

Letcher, Trevor M; Redhi, Gan G; Journal of Chemical Thermodynamics; vol. 33; nb. 11; (2001); p. 1499 - 1509, View in Reaxys 5 of 32

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

113/428

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Partner (Energy Data (MCS))

acetonitrile

Letcher; Redhi; Journal of Chemical and Engineering Data; vol. 45; nb. 1; (2000); p. 57 - 60, View in Reaxys 6 of 32

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Comment (Energy Data (MCS))

concentration dependence

Partner (Energy Data (MCS))

n-heptane

Wilhelm; Inglese; Grolier; Journal of Chemical Thermodynamics; vol. 31; nb. 9; (1999); p. 1165 - 1174, View in Reaxys 7 of 32

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25 - 45

Partner (Energy Data (MCS))

hexane

Ruiz, Alfonso; Journal of Chemical Thermodynamics; vol. 27; nb. 11; (1995); p. 1227 - 1234, View in Reaxys 8 of 32

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

methanol

Lopez, M.; Fernandez, J.; Sarmiento, F.; Legido, J.L.; Romani, L.; et al.; Journal of Chemical Thermodynamics; vol. 24; nb. 8; (1992); p. 809 - 814, View in Reaxys 9 of 32

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

ethanol

Lopez, M.; Fernandez, J.; Sarmiento, F.; Legido, J.L.; Romani, L.; et al.; Journal of Chemical Thermodynamics; vol. 24; nb. 8; (1992); p. 809 - 814, View in Reaxys 10 of 32

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 11 of 32

Description (Energy Data (MCS))

Enthalpy of solution

Partner (Energy Data (MCS))

water

Description (Energy Data (MCS))

Excess thermochemical parameter

114/428

2017-08-01 04:43:04

Temperature (Energy Data (MCS)) [°C]

80.3

Partner (Energy Data (MCS))

n-Nonane

Figurski, G.; Weber, U. v.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 267; nb. 6; (1986); p. 1166 - 1172, View in Reaxys 13 of 32

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

water

Lapshina, I. Z.; Sergeeva, V. F.; Zakumbaeva, Z. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 5; (1984); p. 978 - 982,870 - 873, View in Reaxys 14 of 32

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

2,6-dimethylpyridine

Lapshina, I. Z.; Sergeeva, V. F.; Zakumbaeva, Z. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 5; (1984); p. 978 - 982,870 - 873, View in Reaxys 15 of 32

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

2,6-dimethylpyridine; water

Lapshina, I. Z.; Sergeeva, V. F.; Zakumbaeva, Z. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 5; (1984); p. 978 - 982,870 - 873, View in Reaxys 16 of 32

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

TETRAHYDROPYRANE

Wilhelm, Emmerich; Inglese, A; Grolier, J.-P.E; Kehiaian, H.V; The Journal of Chemical Thermodynamics; vol. 14; nb. 1; (1982); p. 33 - 36, View in Reaxys 17 of 32

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

1,3-DIOXOLANE

Wilhelm, Emmerich; Inglese, A; Grolier, J.-P.E; Kehiaian, H.V; The Journal of Chemical Thermodynamics; vol. 14; nb. 1; (1982); p. 33 - 36, View in Reaxys 18 of 32

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

1,4-dioxane

115/428

2017-08-01 04:43:04

Wilhelm, Emmerich; Inglese, A; Grolier, J.-P.E; Kehiaian, H.V; The Journal of Chemical Thermodynamics; vol. 14; nb. 1; (1982); p. 33 - 36, View in Reaxys 19 of 32

Description (Energy Data (MCS))

Heat capacity of mixtures

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

H2O

Casanova, C.; Emmerich, Wilhelm; Grolier, J.-P. E.; Kehiaian, H. V.; Journal of Chemical Thermodynamics; vol. 13; nb. 3; (1981); p. 241 - 248, View in Reaxys; Harris, Alexander L.; Thompson, Peter T.; Wood, Robert H.; Journal of Solution Chemistry; vol. 9; (1980); p. 305 - 324, View in Reaxys 20 of 32

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

pyridine

Kehlen, H.; Herold, F.; Rademacher, H.-J.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 261; nb. 4; (1980); p. 809 - 812, View in Reaxys 21 of 32

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

pyridine

Kehlen, H.; Herold, F.; Rademacher, H.-J.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 261; nb. 4; (1980); p. 809 - 812, View in Reaxys 22 of 32

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

aniline

Kehlen, H.; Herold, F.; Rademacher, H.-J.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 261; nb. 4; (1980); p. 809 - 812, View in Reaxys 23 of 32

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

aniline

Kehlen, H.; Herold, F.; Rademacher, H.-J.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 261; nb. 4; (1980); p. 809 - 812, View in Reaxys 24 of 32

Description (Energy Data (MCS))

Enthalpy of dilution

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

H2O

Harris, Alexander L.; Thompson, Peter T.; Wood, Robert H.; Journal of Solution Chemistry; vol. 9; (1980); p. 305 - 324, View in Reaxys 25 of 32

Description (Energy Data (MCS))

Excess thermochemical parameter

116/428

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Lindenbaum; Journal of Chemical Thermodynamics; vol. 3; (1971); p. 625,627,628, View in Reaxys; Apelblat, Kohler; Journal of Chemical Thermodynamics; vol. 8; (1976); p. 749,751, 752, 754, 755, View in Reaxys 26 of 32

Description (Energy Data (MCS))

Enthalpy of solution

Aveyard; Mitchell; Transactions of the Faraday Society; vol. 64; (1968); p. 1757,1759, View in Reaxys; Aveyard; Mitchell; Transactions of the Faraday Society; vol. 66; (1970); p. 37,39, View in Reaxys; Larsen; Magid; Journal of Physical Chemistry; vol. 78; (1974); p. 834,836, View in Reaxys 27 of 32

Description (Energy Data (MCS))

Thermodynamic properties of system with

Wright; Akhtar; Transactions of the Faraday Society; vol. 66; (1970); p. 990,993, View in Reaxys; Korenman et al.; Russian Journal of Physical Chemistry; vol. 47; (1973); p. 682; ; p. 1207, View in Reaxys 28 of 32

Description (Energy Data (MCS))

Enthalpy of dilution

Lindenbaum; Journal of Chemical Thermodynamics; vol. 3; (1971); p. 625,627,628, View in Reaxys 29 of 32

Description (Energy Data (MCS))

Enthalpy of evaporation

Motscharnjuk; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 1086,1103; Chem.Abstr.; nb. 23624; (1960), View in Reaxys 30 of 32

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

Partner (Energy Data (MCS))

water

Ketelaar; Loopstra; Recueil des Travaux Chimiques des Pays-Bas; vol. 74; (1955); p. 113,115, View in Reaxys 31 of 32

Description (Energy Data (MCS))

Heat capacity of mixtures

Solvent (Energy Data (MCS))

H2O

Temperature (Energy Data (MCS)) [°C]

13.5 - 16.5

Bury; Davies; Journal of the Chemical Society; (1932); p. 2415, View in Reaxys 32 of 32

Description (Energy Data (MCS))

Heat capacity of mixtures

Solvent (Energy Data (MCS))

H2O

Luedeking; Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften; (1886); p. 216, View in Reaxys Enthalpies of Other Phase Transitions (2) Enthalpies of Oth- Comment (EnReferences er Phase Transi- thalpies of Other tions [Jmol-1] Phase Transitions) -72850.2

From gas-phase to aqueous solution

Wilson, Burton; Georgiadis, Rosina; Bartmess, John E.; Journal of the American Chemical Society; vol. 113; nb. 5; (1991); p. 1762 - 1766, View in Reaxys

1040

From crystal to crystal

Martin, J. F.; Andon, R. J. L.; Journal of Chemical Thermodynamics; vol. 14; nb. 7; (1982); p. 679 - 688, View in Reaxys

Enthalpy of Combustion (1) References Lebedewa; Russian Journal of Physical Chemistry; vol. 38; (1964); p. 1435; Zhurnal Fizicheskoi Khimii; vol. 38; (1964); p. 2648, View in Reaxys Enthalpy of Formation (1) References

117/428

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Borchers; Levsen; International Journal of Mass Spectrometry and Ion Physics; vol. 31; (1979); p. 247,255, View in Reaxys Enthalpy of Fusion (2) Enthalpy of FuReferences sion [Jmol-1] 11590

Martin, J. F.; Andon, R. J. L.; Journal of Chemical Thermodynamics; vol. 14; nb. 7; (1982); p. 679 - 688, View in Reaxys

125771

Parks; Anderson; Journal of the American Chemical Society; vol. 48; (1926); p. 1508, View in Reaxys

Enthalpy of Sublimation (1) References Calis-van Ginkel et al.; Journal of Chemical Thermodynamics; vol. 10; (1978); p. 1083,1087, 1088, View in Reaxys Enthalpy of Vaporization (3) Enthalpy of VaTemperature (Enporization thalpy of Vapori[Jmol-1] zation) [°C] 63600

Comment (Enthalpy of Vaporization)

References

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 Konicek; Wadsoe; Acta Chemica Scandinavica (1947-1973); vol. 24; (1970); p. 2612, View in Reaxys

72808.4

at:15-40 degreeC. Skljarenko et al.; Zhurnal Fizicheskoi Khimii; vol. 32; (1958); p. 692,695; Chem.Abstr.; (1958); p. 14266, View in Reaxys

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Reynaud; Bulletin de la Societe Chimique de France; (1968); p. 3945, View in Reaxys

Further information

Jansson et al.; Suomen Kemistilehti B; vol. 41; (1968); p. 281, View in Reaxys

Further information

Sigman; Journal of Biological Chemistry; vol. 242; (1967); p. 3815,3818, View in Reaxys

Further information

Okamoto et al.; Bulletin of the Chemical Society of Japan; vol. 40; (1967); p. 1905,1908, View in Reaxys

Further information

Meeussen et al.; Bulletin des Societes Chimiques Belges; vol. 76; (1967); p. 145,150,153, View in Reaxys

Further information

Occolowitz; Australian Journal of Chemistry; vol. 20; (1967); p. 2387,2388, View in Reaxys

121/428

2017-08-01 04:43:04

Further information

Statz; Lippert; Berichte der Bunsen-Gesellschaft; vol. 71; (1967); p. 673, View in Reaxys

Further information

Conti; Franconi; Berichte der Bunsen-Gesellschaft; vol. 71; (1967); p. 146, View in Reaxys

Further information

Bhowmik; Palit; Journal of the Indian Chemical Society; vol. 44; (1967); p. 1049,1053, View in Reaxys

Further information

Fialkov; Borovikov; Sov. Prog. Chem. (Engl. Transl.); vol. 32; (1966); p. 590,450, View in Reaxys

Further information

Suga; Matsuura; Bulletin of the Chemical Society of Japan; vol. 39; (1966); p. 326,328, View in Reaxys

Further information

Silver et al.; Journal of Physical Chemistry; vol. 70; (1966); p. 1434,1436, View in Reaxys

Further information

Eisen; Joffe; Journal of Chemical and Engineering Data; vol. 11; (1966); p. 480, View in Reaxys

Further information

Khimenko; Golub; Sov. Prog. Chem. (Engl. Transl.); vol. 32; (1966); p. 161,125, View in Reaxys

Further information

Murty et al.; Journal of Chemical and Engineering Data; vol. 11; (1966); p. 335, View in Reaxys

Further information

Benjamin; Journal of Physical Chemistry; vol. 70; (1966); p. 3790,3794, View in Reaxys

Further information

Simon et al.; Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,; vol. 21; (1966); p. 1115, View in Reaxys

Further information

Paul et al.; Indian Journal of Chemistry; vol. 3; (1965); p. 239, View in Reaxys

Further information

Adema; Schrama; Analytical Chemistry; vol. 37; (1965); p. 229,230, View in Reaxys

Further information

Rao; Murty; Journal of Chemical and Engineering Data; vol. 10; (1965); p. 248, View in Reaxys

Further information

Konovalov; Russian Journal of Physical Chemistry; vol. 39; (1965); p. 364; ; p. 693, View in Reaxys

Further information

Musakin; Chih-Li; Russian Journal of Physical Chemistry; vol. 39; (1965); p. 39; ; p. 79, View in Reaxys

Further information

Shimbashi; Shiba; Bulletin of the Chemical Society of Japan; vol. 38; (1965); p. 572,581, 588, View in Reaxys

Further information

Kirby et al.; Journal of the American Oil Chemists' Society; vol. 42; (1965); p. 437,440, View in Reaxys

Further information

Aplin et al.; Journal of the American Chemical Society; vol. 87; (1965); p. 3180,3182, View in Reaxys

Further information

Wolf; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 225; (1964); p. 1,9, View in Reaxys

Further information

Lebedewa; Russian Journal of Physical Chemistry; vol. 38; (1964); p. 1435; Zhurnal Fizicheskoi Khimii; vol. 38; (1964); p. 2648, View in Reaxys

Further information

Constant; Lebrun; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 61; (1964); p. 163,164,167,168,171, View in Reaxys

Further information

Herzog; Kalies; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 329; (1964); p. 83,84,87, View in Reaxys

Further information

Ampilogow; Russian Journal of Physical Chemistry; vol. 38; (1964); p. 740; Zhurnal Fizicheskoi Khimii; vol. 38; (1964); p. 1350, View in Reaxys

Further information

Sarachani; Winnik; Russian Journal of Physical Chemistry; vol. 38; (1964); p. 332; Zhurnal Fizicheskoi Khimii; vol. 38; (1964); p. 632, View in Reaxys

Further information

Hertz; Zeidler; Berichte der Bunsen-Gesellschaft; vol. 68; (1964); p. 821,830, 833, View in Reaxys

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Further information

Barrer; Locke; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 40; (1964); p. 301,304, View in Reaxys

Further information

Sell; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 39; (1963); p. 322,327, View in Reaxys

Further information

Palluy et al.; Helvetica Chimica Acta; vol. 46; (1963); p. 2297, View in Reaxys

Further information

Snobl et al.; Collection of Czechoslovak Chemical Communications; vol. 28; (1963); p. 436,437, View in Reaxys

Further information

Ellis; Journal of the Chemical Society; (1963); p. 2299,2302, View in Reaxys

Further information

Segerman; Acta Crystallographica; vol. 16; (1963); p. A76, View in Reaxys

Further information

Khomutov et al.; Russian Journal of Physical Chemistry; vol. 37; (1963); p. 93; ; p. 189, View in Reaxys

Further information

Misniakiewicz; Zeszyty Naukowe Politechniki Slaskiej, Chemia; vol. 14; (1963); p. 1,28,33,39,40,48,56,57, View in Reaxys

Further information

Jones; Canadian Journal of Chemistry; vol. 40; (1962); p. 321, View in Reaxys

Further information

Flett,M.S.C.; Spectrochimica Acta; vol. 18; (1962); p. 1537 - 1556, View in Reaxys

Further information

Beroza; Analytical Chemistry; vol. 34; (1962); p. 1801,1802, View in Reaxys

Further information

Dawydow; Lisowina; Zhurnal Fizicheskoi Khimii; vol. 36; (1962); p. 1993; ; p. 1072, View in Reaxys

Further information

Paul et al.; Journal of the Indian Chemical Society; vol. 39; (1962); p. 297, View in Reaxys

Further information

Prevot; Bulletin de la Societe Chimique de France; (1962); p. 670, View in Reaxys

Further information

Normant; Angelo; Bulletin de la Societe Chimique de France; (1962); p. 814, 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

v. Engelhardt; Hinrichsen; Zeitschrift fuer Elektrochemie; vol. 65; (1961); p. 793, View in Reaxys

Further information

Sokolow et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 1051,971; Chem.Abstr.; nb. 20593; (1961), View in Reaxys

Further information

Levitt; Chemistry and Industry (London, United Kingdom); (1961); p. 1621, View in Reaxys

Further information

Emery; Koerner; Analytical Chemistry; vol. 33; (1961); p. 146, View in Reaxys

Further information

Sriraman; Thiruvengadathan; Bulletin of the Chemical Society of Japan; vol. 34; (1961); p. 1560, View in Reaxys

Further information

Gray et al.; Analytical Chemistry; vol. 32; (1960); p. 582,584, View in Reaxys

Further information

Hatcher et al.; Journal of Chemical Physics; vol. 32; (1960); p. 28,29, View in Reaxys

Further information

Ralls; Analytical Chemistry; vol. 32; (1960); p. 332, View in Reaxys

Further information

Elatrash et al.; Journal of Physical Chemistry; vol. 64; (1960); p. 785, View in Reaxys

Further information

Ssokolow; Potschtakowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 1401,1429; Chem.Abstr.; nb. 23685; (1960), View in Reaxys

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Further information

Taeufel et al.; Naturwissenschaften; vol. 47; (1960); p. 355, View in Reaxys

Further information

Hunter et al.; Analytical Chemistry; vol. 32; (1960); p. 1757, View in Reaxys

Further information

Ssumarokowa; Nurmakowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 29,29; Chem.Abstr.; nb. 19134; (1960), View in Reaxys

Further information

Janak et al.; Collection of Czechoslovak Chemical Communications; vol. 25; (1960); p. 1566, View in Reaxys

Further information

Mueller et al.; Analytical Chemistry; vol. 32; (1960); p. 687, View in Reaxys

Further information

Okubo; Goto; Nippon Kagaku Zasshi; vol. 81; (1960); p. 1132,1133-1136; Chem.Abstr.; nb. 3342; (1962), View in Reaxys

Further information

Howe; Journal of Chromatography; vol. 3; (1960); p. 389,390-405; Chem.Abstr.; vol. 55; nb. 7267; (1961), View in Reaxys

Further information

Zindrik; Ssokolow; J. Gen. Chem. USSR (Engl. Transl.); vol. 28; (1958); p. 1728,1775; Chem.Abstr.; nb. 19414; (1958), View in Reaxys

Gas Phase (3) Description (Gas Phase)

Comment (Gas Phase)

Association in the gas phase

References Kollar; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 235; (1967); p. 281, View in Reaxys; Miyamoto, Shinji; Nakamura, Shinichi; Iwai, Yoshio; Arai, Yasuhiko; Journal of Chemical and Engineering Data; vol. 44; nb. 1; (1999); p. 48 - 51, View in Reaxys

Association in the gas phase

Enthalpie der binaeren Assoziation in der Dampfphase (aus dem IR-Spektrum ermittelt) bei 10-15grad.

Lundin et al.; Journal of the American Chemical Society; vol. 74; (1952); p. 743, View in Reaxys; Clague; Bernstein; Spectrochimica Acta; vol. 25 A; (1969); p. 593,596, View in Reaxys

Association in the gas phase

Assoziationsgrad und Dissoziationswaerme des Assoziats in der Dampfphase (aus dem IR-Spektrum ermittelt).

Schubin; Izvestiya Akademii Nauk SSSR, Seriya Fizicheskaya; vol. 14; (1950); p. 442,445,446; Chem.Abstr.; (1951); p. 3245, View in Reaxys; Schubin; Trudy fiz.Inst.Akad.S.S.S.R.; vol. 2; (1958); p. 127,165,171; Chem.Abstr.; (1959); p. 9812, View in Reaxys

Heat Capacity Cp (9) Heat Capacity Cp Temperature [Jmol-1K-1] (Heat Capacity Cp) [°C]

Comment (Heat Capacity Cp)

References

176000

19.99

Liquid

Bahadur; Singh; Deenadayalu; Naidoo; Ramjugernath; Thermochimica Acta; vol. 590; (2014); p. 151 - 159, View in Reaxys

178000

24.99

Liquid

Bahadur; Singh; Deenadayalu; Naidoo; Ramjugernath; Thermochimica Acta; vol. 590; (2014); p. 151 - 159, View in Reaxys

180000

29.99

Liquid

Bahadur; Singh; Deenadayalu; Naidoo; Ramjugernath; Thermochimica Acta; vol. 590; (2014); p. 151 - 159, View in Reaxys

182000

34.99

Liquid

Bahadur; Singh; Deenadayalu; Naidoo; Ramjugernath; Thermochimica Acta; vol. 590; (2014); p. 151 - 159, View in Reaxys

184000

39.99

Liquid

Bahadur; Singh; Deenadayalu; Naidoo; Ramjugernath; Thermochimica Acta; vol. 590; (2014); p. 151 - 159, View in Reaxys

5.81 - 209.1

-257 - 99.9

Martin, J. F.; Andon, R. J. L.; Journal of Chemical Thermodynamics; vol. 14; nb. 7; (1982); p. 679 - 688, View in Reaxys

177.33

Casanova, C.; Emmerich, Wilhelm; Grolier, J.-P. E.; Kehiaian, H. V.; Journal of Chemical Thermodynamics; vol. 13; nb. 3; (1981); p. 241 - 248, View in Reaxys

124/428

2017-08-01 04:43:04

63.45 - 135.75

89.2 - 231.5

Parks; Anderson; Journal of the American Chemical Society; vol. 48; (1926); p. 1508, View in Reaxys

171.17 - 176.33

274.8 - 290.7

Parks; Anderson; Journal of the American Chemical Society; vol. 48; (1926); p. 1508, View in Reaxys

Interatomic Distances and Angles (3) Description Comment (Intera- References tomic Distances and Angles) Interatomic distances and angles

Strieter; Templeton; Acta Crystallographica; vol. 15; (1962); p. 1240,1243, View in Reaxys; Kanters et al.; Tetrahedron; vol. 23; (1967); p. 4027,4028,4031, View in Reaxys

Interatomic distances and angles

von krystalliner Strieter; U.S.Atomic Energy Comm.UCRL-8906; <1959>30, View in Reaxys; Strieter; Buttersaeure (aus Templeton; Acta Crystallographica; vol. 15; (1962); p. 1240,1243, View in Reaxys dem RoentgenDiagramm ermittelt).

Interatomic distances and angles

Laenge der Was- Strieter; U.S.Atomic Energy Comm.UCRL-8906; <1959>30, View in Reaxys; Strieter; serstoff-Bruecken Templeton; Acta Crystallographica; vol. 15; (1962); p. 1240,1243, View in Reaxys in krystalliner Buttersaeure bei -43grad (aus dem Roentgen-Diagramm ermittelt).

Ionization Potential (4) Ionization Poten- Method (Ionizatial [eV] tion Potential)

Comment (Ioniza- References tion Potential)

10.17

Type: adiabatic

Butler, James J.; Fraser-Monteiro, Maria L.; Fraser-Monteiro, Luis; Baer, Tomas; Hass, J. Ronald; Journal of Physical Chemistry; vol. 86; nb. 5; (1982); p. 747 - 752, View in Reaxys

Type: adiabatic

Holmes, John L.; Fingas, Mervin; Lossing, F. P.; Canadian Journal of Chemistry; vol. 59; (1981); p. 80 - 93, View in Reaxys

Photoionization

10.24

Benoit; Harrison; Journal of the American Chemical Society; vol. 99; (1977); p. 3980,3981, View in Reaxys; Occolowitz; Australian Journal of Chemistry; vol. 20; (1967); p. 2387,2388, View in Reaxys; Watanabe et al.; Journal of Quantitative Spectroscopy and Radiative Transfer; vol. 2; (1962); p. 369,377, View in Reaxys; Watanabe et al.; Bulletin of the Chemical Society of Japan; vol. 46; (1973); p. 1959,1960, 1962, View in Reaxys; Poldoja; Palm; Organic Reactivity (New York, English Translation); vol. 4; (1967); p. 320,329, View in Reaxys 10.22

Electron impact

Morrison; Nicholson; Journal of Chemical Physics; vol. 20; (1952); p. 1021, View in Reaxys

Kinematic Viscosity (1) References Kotorlenko; Ukrainskii Khimicheskii Zhurnal (Russian Edition); vol. 28; (1962); p. 333,334, View in Reaxys Liquid Phase (14) Description (LiqComment (Liquid uid Phase) Phase)

References

Association in the liquid state

Jakobsen et al.; Spectrochimica Acta; vol. 25A; (1969); p. 839, View in Reaxys; Rao; Rao; Journal of Scientific and Industrial Research, Section B: Physical Sciences; vol. 21; (1962); p. 331,332, View in Reaxys; 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

Self-association in solution

Luong The Man et al.; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 260; (1965); p. 2755 - 2758, View in Reaxys; Palm; Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,; vol. 22; (1967); p. 57, View in Reaxys; Korenman; Gur'ev; J. Anal. Chem. USSR (Engl. Transl.); vol. 30; (1975); p. 1601, View in Reaxys; Yamamoto; Nishi; Journal of the American Chemical Society; vol. 112; nb. 2; (1990); p. 549 - 558, View in Reaxys; Tanaka, Naoki; Kitano, Hiromi; Ise, Norio; Journal of Physical Chemistry; vol. 94; nb. 16; (1990); p. 6290 -

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6292, View in Reaxys; Salomon, Mark; Journal of Solution Chemistry; vol. 15; nb. 3; (1986); p. 237 - 242, View in Reaxys Structure of the liquid

Luzkii; Michailenko; Russian Journal of Physical Chemistry; vol. 38; (1964); p. 775; Zhurnal Fizicheskoi Khimii; vol. 38; (1964); p. 1414, View in Reaxys

Self-association in solution

Konstante der binaeren Assoziation (potentiometrisch ermittelt) in Wasser bei 15 45grad.

Martin; Rossotti; Proceedings of the Chemical Society, London; (1959); p. 60; Proceedings of the Chemical Society, London; (1961); p. 73, View in Reaxys; Nash; Monk; Journal of the Chemical Society; (1957); p. 4274,4279, View in Reaxys

Association in the liquid state

Assoziationsgrad. Tyuzyo; Bulletin of the Chemical Society of Japan; vol. 30; (1957); p. 782,851, View in Reaxys

Self-association in solution

in Tetrachlormethan.

Wenograd; Spurr; Journal of the American Chemical Society; vol. 79; (1957); p. 5844, View in Reaxys

Self-association in solution

Assoziationsgrad (aus dem IRSpektrum ermittelt) in Paraffinoel bei 98 - 161grad.

Sarkadi; de Boer; Recueil des Travaux Chimiques des Pays-Bas; vol. 76; (1957); p. 628,639,644, View in Reaxys

Self-association in solution

Assoziationsgrad wss.Loesung bei 0grad.

Davies; Griffith; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 6; (1956); p. 143, View in Reaxys

Self-association in solution

Konstante der binaeren Assoziation in Benzol bei 6.3grad.

Davies; Griffith; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 6; (1956); p. 143, View in Reaxys

Self-association in solution

Konstante der bi- Cartwright; Monk; Journal of the Chemical Society; (1955); p. 2500, View in Reaxys naeren Assoziation (konduktometrisch ermittelt) in Wasser bei 25grad.

Self-association in solution

in Benzol (aus der Pohl; Hobbs; Gross; Journal of Chemical Physics; vol. 9; (1941); p. 413, dielektrischen Po- View in Reaxys larisation).

Self-association in solution

in Benzol (kryoskopisch).

Meisenheimer; Dorner; Justus Liebigs Annalen der Chemie; vol. 523; (1936); p. 301, View in Reaxys

Self-association in solution

in Cyclohexan (kryoskopisch).

Broughton; Transactions of the Faraday Society; vol. 30; (1934); p. 368, View in Reaxys

Self-association in solution

in Phenolloesung. Robertson; Journal of the Chemical Society; vol. 83; (1903); p. 1428, View in Reaxys

Liquid/Liquid Systems (MCS) (160) 1 of 160

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25.04

Partner (Liquid/Liquid Systems (MCS))

cyclohexane; water

Ghanadzadeh; Asgharzadeh; Dastmoozeh; Thermochimica Acta; vol. 523; nb. 1-2; (2011); p. 154 - 160, View in Reaxys 2 of 160

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

30.04

126/428

2017-08-01 04:43:04

Partner (Liquid/Liquid Systems (MCS))

cyclohexane; water

Ghanadzadeh; Asgharzadeh; Dastmoozeh; Thermochimica Acta; vol. 523; nb. 1-2; (2011); p. 154 - 160, View in Reaxys 3 of 160

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

35.04

Partner (Liquid/Liquid Systems (MCS))

cyclohexane; water

Ghanadzadeh; Asgharzadeh; Dastmoozeh; Thermochimica Acta; vol. 523; nb. 1-2; (2011); p. 154 - 160, View in Reaxys 4 of 160

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

40.04

Partner (Liquid/Liquid Systems (MCS))

cyclohexane; water

Ghanadzadeh; Asgharzadeh; Dastmoozeh; Thermochimica Acta; vol. 523; nb. 1-2; (2011); p. 154 - 160, View in Reaxys 5 of 160

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

5 - 55

Partner (Liquid/Liquid Systems (MCS))

water; pyridine

Cherkasov; Smotrov; Il'in; Russian Journal of Applied Chemistry; vol. 81; nb. 2; (2008); p. 218 - 222, View in Reaxys 6 of 160

Description (Liquid/ Liquid Systems (MCS))

Solubility diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.99

Partner (Liquid/Liquid Systems (MCS))

dimethyl succinate; H2O

Kirbaslar, S. Ismail; Sahin, Selin; Bilgin, Mehmet; Journal of Chemical Thermodynamics; vol. 39; nb. 2; (2007); p. 284 - 290, View in Reaxys 7 of 160

Description (Liquid/ Liquid Systems (MCS))

Solubility diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.99

Partner (Liquid/Liquid Systems (MCS))

dimethyl glutarate; H2O

Kirbaslar, S. Ismail; Sahin, Selin; Bilgin, Mehmet; Journal of Chemical Thermodynamics; vol. 39; nb. 2; (2007); p. 284 - 290, View in Reaxys 8 of 160

Description (Liquid/ Liquid Systems (MCS))

Solubility diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.99

127/428

2017-08-01 04:43:04

Partner (Liquid/Liquid Systems (MCS))

dimethyl adipate; H2O

Kirbaslar, S. Ismail; Sahin, Selin; Bilgin, Mehmet; Journal of Chemical Thermodynamics; vol. 39; nb. 2; (2007); p. 284 - 290, View in Reaxys 9 of 160

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.99

Partner (Liquid/Liquid Systems (MCS))

dimethyl adipate; H2O

Kirbaslar, S. Ismail; Sahin, Selin; Bilgin, Mehmet; Journal of Chemical Thermodynamics; vol. 39; nb. 2; (2007); p. 284 - 290, View in Reaxys 10 of 160

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.99

Partner (Liquid/Liquid Systems (MCS))

dimethyl glutarate; H2O

Kirbaslar, S. Ismail; Sahin, Selin; Bilgin, Mehmet; Journal of Chemical Thermodynamics; vol. 39; nb. 2; (2007); p. 284 - 290, View in Reaxys 11 of 160

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.99

Partner (Liquid/Liquid Systems (MCS))

dimethyl succinate; H2O

Kirbaslar, S. Ismail; Sahin, Selin; Bilgin, Mehmet; Journal of Chemical Thermodynamics; vol. 39; nb. 2; (2007); p. 284 - 290, View in Reaxys 12 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.99

Partner (Liquid/Liquid Systems (MCS))

dimethyl succinate; H2O

Kirbaslar, S. Ismail; Sahin, Selin; Bilgin, Mehmet; Journal of Chemical Thermodynamics; vol. 39; nb. 2; (2007); p. 284 - 290, View in Reaxys 13 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.99

Partner (Liquid/Liquid Systems (MCS))

dimethyl glutarate; H2O

Kirbaslar, S. Ismail; Sahin, Selin; Bilgin, Mehmet; Journal of Chemical Thermodynamics; vol. 39; nb. 2; (2007); p. 284 - 290, View in Reaxys 14 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.99

128/428

2017-08-01 04:43:04

Partner (Liquid/Liquid Systems (MCS))

dimethyl adipate; H2O

Kirbaslar, S. Ismail; Sahin, Selin; Bilgin, Mehmet; Journal of Chemical Thermodynamics; vol. 39; nb. 2; (2007); p. 284 - 290, View in Reaxys 15 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Comment (Liquid/Liquid Systems (MCS))

ambient temperature

Partner (Liquid/Liquid Systems (MCS))

polypropylene glycol, average molecular weight: 3500, functionality: 1.7; water

Ashraf; Bukhari; Polish Journal of Chemistry; vol. 81; nb. 9; (2007); p. 1621 - 1628, View in Reaxys 16 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

in the presence of additives

Partner (Liquid/Liquid Systems (MCS))

i-Amyl alcohol

Bilgin, Mehmet; Ismail Kirbaslar; Oezean, Oender; Dramur, Umur; Journal of Chemical and Engineering Data; vol. 51; nb. 5; (2006); p. 1546 - 1550, View in Reaxys 17 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

in the presence of additives

Partner (Liquid/Liquid Systems (MCS))

nonyl alcohol

Bilgin, Mehmet; Ismail Kirbaslar; Oezean, Oender; Dramur, Umur; Journal of Chemical and Engineering Data; vol. 51; nb. 5; (2006); p. 1546 - 1550, View in Reaxys 18 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

in the presence of additives

Partner (Liquid/Liquid Systems (MCS))

1-Decanol

Bilgin, Mehmet; Ismail Kirbaslar; Oezean, Oender; Dramur, Umur; Journal of Chemical and Engineering Data; vol. 51; nb. 5; (2006); p. 1546 - 1550, View in Reaxys 19 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

in the presence of additives

Partner (Liquid/Liquid Systems (MCS))

1-dodecyl alcohol

129/428

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Bilgin, Mehmet; Ismail Kirbaslar; Oezean, Oender; Dramur, Umur; Journal of Chemical and Engineering Data; vol. 51; nb. 5; (2006); p. 1546 - 1550, View in Reaxys 20 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

in the presence of additives

Partner (Liquid/Liquid Systems (MCS))

oleyl alcohol

Bilgin, Mehmet; Ismail Kirbaslar; Oezean, Oender; Dramur, Umur; Journal of Chemical and Engineering Data; vol. 51; nb. 5; (2006); p. 1546 - 1550, View in Reaxys 21 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

in the presence of additives

Partner (Liquid/Liquid Systems (MCS))

butanone

Bilgin, Mehmet; Ismail Kirbaslar; Oezean, Oender; Dramur, Umur; Journal of Chemical and Engineering Data; vol. 51; nb. 5; (2006); p. 1546 - 1550, View in Reaxys 22 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

in the presence of additives

Partner (Liquid/Liquid Systems (MCS))

3-methyl-butan-2-one

Bilgin, Mehmet; Ismail Kirbaslar; Oezean, Oender; Dramur, Umur; Journal of Chemical and Engineering Data; vol. 51; nb. 5; (2006); p. 1546 - 1550, View in Reaxys 23 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

in the presence of additives

Partner (Liquid/Liquid Systems (MCS))

4- methyl-2-pentanone

Bilgin, Mehmet; Ismail Kirbaslar; Oezean, Oender; Dramur, Umur; Journal of Chemical and Engineering Data; vol. 51; nb. 5; (2006); p. 1546 - 1550, View in Reaxys 24 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

in the presence of additives

130/428

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Partner (Liquid/Liquid Systems (MCS))

4-heptanone

Bilgin, Mehmet; Ismail Kirbaslar; Oezean, Oender; Dramur, Umur; Journal of Chemical and Engineering Data; vol. 51; nb. 5; (2006); p. 1546 - 1550, View in Reaxys 25 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

in the presence of additives

Partner (Liquid/Liquid Systems (MCS))

ethyl acetate

Bilgin, Mehmet; Ismail Kirbaslar; Oezean, Oender; Dramur, Umur; Journal of Chemical and Engineering Data; vol. 51; nb. 5; (2006); p. 1546 - 1550, View in Reaxys 26 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

in the presence of additives

Partner (Liquid/Liquid Systems (MCS))

cyclohexyl acetate

Bilgin, Mehmet; Ismail Kirbaslar; Oezean, Oender; Dramur, Umur; Journal of Chemical and Engineering Data; vol. 51; nb. 5; (2006); p. 1546 - 1550, View in Reaxys 27 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

in the presence of additives

Partner (Liquid/Liquid Systems (MCS))

phthalic acid dimethyl ester

Bilgin, Mehmet; Ismail Kirbaslar; Oezean, Oender; Dramur, Umur; Journal of Chemical and Engineering Data; vol. 51; nb. 5; (2006); p. 1546 - 1550, View in Reaxys 28 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

in the presence of additives

Partner (Liquid/Liquid Systems (MCS))

phthalic acid dibutyl ester

Bilgin, Mehmet; Ismail Kirbaslar; Oezean, Oender; Dramur, Umur; Journal of Chemical and Engineering Data; vol. 51; nb. 5; (2006); p. 1546 - 1550, View in Reaxys 29 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

131/428

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Comment (Liquid/Liquid Systems (MCS))

in the presence of additives

Partner (Liquid/Liquid Systems (MCS))

tert-butyl methyl ether

Bilgin, Mehmet; Ismail Kirbaslar; Oezean, Oender; Dramur, Umur; Journal of Chemical and Engineering Data; vol. 51; nb. 5; (2006); p. 1546 - 1550, View in Reaxys 30 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

in the presence of additives

Partner (Liquid/Liquid Systems (MCS))

toluene

Bilgin, Mehmet; Ismail Kirbaslar; Oezean, Oender; Dramur, Umur; Journal of Chemical and Engineering Data; vol. 51; nb. 5; (2006); p. 1546 - 1550, View in Reaxys 31 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

in the presence of additives

Partner (Liquid/Liquid Systems (MCS))

hexane

Bilgin, Mehmet; Ismail Kirbaslar; Oezean, Oender; Dramur, Umur; Journal of Chemical and Engineering Data; vol. 51; nb. 5; (2006); p. 1546 - 1550, View in Reaxys 32 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.99 - 44.99

Partner (Liquid/Liquid Systems (MCS))

oleyl alcohol; H2O

Bilgin, Mehmet; Journal of Chemical Thermodynamics; vol. 38; nb. 12; (2006); p. 1634 - 1639, View in Reaxys 33 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.99 - 44.99

Partner (Liquid/Liquid Systems (MCS))

oleyl alcohol; H2O

Bilgin, Mehmet; Journal of Chemical Thermodynamics; vol. 38; nb. 12; (2006); p. 1634 - 1639, View in Reaxys 34 of 160

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.99 - 44.99

Partner (Liquid/Liquid Systems (MCS))

oleyl alcohol; H2O

Bilgin, Mehmet; Journal of Chemical Thermodynamics; vol. 38; nb. 12; (2006); p. 1634 - 1639, View in Reaxys

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35 of 160

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25 - 45

Partner (Liquid/Liquid Systems (MCS))

cyclohexyl acetate

Kirbaslar, S. Ismail; Bilgin, Mehmet; Batr, Deniz; Journal of Chemical Thermodynamics; vol. 37; nb. 2; (2005); p. 175 - 180, View in Reaxys 36 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Partner (Liquid/Liquid Systems (MCS))

cyclohexyl acetate

Kirbaslar, S. Ismail; Bilgin, Mehmet; Batr, Deniz; Journal of Chemical Thermodynamics; vol. 37; nb. 2; (2005); p. 175 - 180, View in Reaxys 37 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25 - 45

Partner (Liquid/Liquid Systems (MCS))

i-Amyl alcohol

Bilgin, Mehmet; Kirbaslar, S. Ismail; Oezcan, Oender; Dramur, Umur; Journal of Chemical Thermodynamics; vol. 37; nb. 4; (2005); p. 297 - 303, View in Reaxys 38 of 160

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25 - 45

Partner (Liquid/Liquid Systems (MCS))

i-Amyl alcohol

Bilgin, Mehmet; Kirbaslar, S. Ismail; Oezcan, Oender; Dramur, Umur; Journal of Chemical Thermodynamics; vol. 37; nb. 4; (2005); p. 297 - 303, View in Reaxys 39 of 160

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

phosphoric acid tributyl ester; dodecane

Morales, Areli Flores; Albet, Joel; Kyuchoukov, George; Malmary, Guy; Molinier, Jacques; Journal of Chemical and Engineering Data; vol. 48; nb. 4; (2003); p. 874 - 886, View in Reaxys 40 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

phosphoric acid tributyl ester; dodecane

Morales, Areli Flores; Albet, Joel; Kyuchoukov, George; Malmary, Guy; Molinier, Jacques; Journal of Chemical and Engineering Data; vol. 48; nb. 4; (2003); p. 874 - 886, View in Reaxys 41 of 160

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

133/428

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Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

Tri-n-octylamine; 1-Decanol; dodecane

Morales, Areli Flores; Albet, Joel; Kyuchoukov, George; Malmary, Guy; Molinier, Jacques; Journal of Chemical and Engineering Data; vol. 48; nb. 4; (2003); p. 874 - 886, View in Reaxys 42 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

Tri-n-octylamine; 1-Decanol; dodecane

Morales, Areli Flores; Albet, Joel; Kyuchoukov, George; Malmary, Guy; Molinier, Jacques; Journal of Chemical and Engineering Data; vol. 48; nb. 4; (2003); p. 874 - 886, View in Reaxys 43 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

pH dependence. Object(s) of Study: concentration dependence

Partner (Liquid/Liquid Systems (MCS))

tri-n-octylamine/decane-1-ol/dodecane - H2O

Morales, Areli Flores; Albet, Joel; Kyuchoukov, George; Malmary, Guy; Molinier, Jacques; Journal of Chemical and Engineering Data; vol. 48; nb. 4; (2003); p. 874 - 886, View in Reaxys 44 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

pH dependence. Object(s) of Study: concentration dependence

Partner (Liquid/Liquid Systems (MCS))

tri-n-butyl phosphate/dodecane - H2O

Morales, Areli Flores; Albet, Joel; Kyuchoukov, George; Malmary, Guy; Molinier, Jacques; Journal of Chemical and Engineering Data; vol. 48; nb. 4; (2003); p. 874 - 886, View in Reaxys 45 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.85

Partner (Liquid/Liquid Systems (MCS))

Tri-n-octylamine; octanol

Li, Zhenyu; Qin, Wei; Dai, Youyuan; Journal of Chemical and Engineering Data; vol. 47; nb. 4; (2002); p. 843 848, View in Reaxys 46 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.85

Partner (Liquid/Liquid Systems (MCS))

Tri-n-octylamine; chloroform

134/428

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Li, Zhenyu; Qin, Wei; Dai, Youyuan; Journal of Chemical and Engineering Data; vol. 47; nb. 4; (2002); p. 843 848, View in Reaxys 47 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.85

Partner (Liquid/Liquid Systems (MCS))

Tri-n-octylamine; 4- methyl-2-pentanone

Li, Zhenyu; Qin, Wei; Dai, Youyuan; Journal of Chemical and Engineering Data; vol. 47; nb. 4; (2002); p. 843 848, View in Reaxys 48 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.85

Partner (Liquid/Liquid Systems (MCS))

Tri-n-octylamine; tetrachloromethane

Li, Zhenyu; Qin, Wei; Dai, Youyuan; Journal of Chemical and Engineering Data; vol. 47; nb. 4; (2002); p. 843 848, View in Reaxys 49 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

acetonitrile; cyclohexane

Letcher, Trevor M.; Redhi, Gan G.; Journal of Chemical Thermodynamics; vol. 33; nb. 12; (2001); p. 1643 - 1653, View in Reaxys 50 of 160

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

acetonitrile; cyclohexane

Letcher, Trevor M.; Redhi, Gan G.; Journal of Chemical Thermodynamics; vol. 33; nb. 12; (2001); p. 1643 - 1653, View in Reaxys 51 of 160

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

benzonitrile

Letcher; Redhi; Journal of Chemical Thermodynamics; vol. 33; nb. 11; (2001); p. 1555 - 1565, View in Reaxys 52 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

14.85

Partner (Liquid/Liquid Systems (MCS))

H2O/trialkylphosphine oxide + kerosene

135/428

2017-08-01 04:43:04

Wang, Yundong; Li, Yuxin; Li, Yi; Wang, Jingyi; Li, Zhenyu; Dai, Youyuan; Journal of Chemical and Engineering Data; vol. 46; nb. 4; (2001); p. 831 - 837, View in Reaxys 53 of 160

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 54 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

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 55 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

n-heptane; acetonitrile

Letcher; Redhi; Journal of Chemical and Engineering Data; vol. 44; nb. 6; (1999); p. 1183 - 1186, View in Reaxys 56 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O

Partner (Liquid/Liquid Systems (MCS))

1,2-dichloro-ethane

Steyaert, Guillaume; Lisa, Guiseppe; Gaillard, Patrick; Boss, Gilles; Reymond, Frederic; Girault, Hubert H.; Carrupt, Pierre-Alain; Testa, Bernard; Journal of the Chemical Society - Faraday Transactions; vol. 93; nb. 3; (1997); p. 401 - 406, View in Reaxys 57 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

4- methyl-2-pentanone; water

Govindarajan; Sabarathinam; Journal of Chemical and Engineering Data; vol. 42; nb. 2; (1997); p. 402 - 408, View in Reaxys 58 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

4- methyl-2-pentanone; water, NaCl, NaNO3, Na2SO4, ZnSO4, (NH4)2SO4

Govindarajan; Sabarathinam; Journal of Chemical and Engineering Data; vol. 42; nb. 2; (1997); p. 402 - 408, View in Reaxys

136/428

2017-08-01 04:43:04

59 of 160

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 60 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

35 - 75

Partner (Liquid/Liquid Systems (MCS))

crude oil INEL / water (pH = 4 - 7)

Reinsel, Mark A.; Borkowski, John J.; Sears, John T.; Journal of Chemical & Engineering Data; vol. 39; nb. 3; (1994); p. 513 - 516, View in Reaxys 61 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

35 - 75

Partner (Liquid/Liquid Systems (MCS))

crude oil ARCO / water (pH = 4 - 7)

Reinsel, Mark A.; Borkowski, John J.; Sears, John T.; Journal of Chemical & Engineering Data; vol. 39; nb. 3; (1994); p. 513 - 516, View in Reaxys 62 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Partner (Liquid/Liquid Systems (MCS))

cetane; water

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Partner (Liquid/Liquid Systems (MCS))

2-cyanoethyl ether; water

Zhuravleva, I. K.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 11.1; (1989); p. 2424 - 2431,2167 - 2172, View in Reaxys 64 of 160

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Partner (Liquid/Liquid Systems (MCS))

2-cyanoethyl ether; water

Zhuravleva, I. K.; J. Gen. Chem. USSR (Engl. Transl.); vol. 59; nb. 11.1; (1989); p. 2424 - 2431,2167 - 2172, View in Reaxys 65 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O

Partner (Liquid/Liquid Systems (MCS))

octanol

Kamlet, Mortimer J.; Doherty, Ruth M.; Abraham, Michael H.; Marcus, Yizhak; Taft, Robert W.; Journal of Physical Chemistry; vol. 92; nb. 18; (1988); p. 5244 - 5255, View in Reaxys 66 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

137/428

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Solvent (Liquid/Liquid Systems (MCS))

H2O; aq. NaOH

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.9

Partner (Liquid/Liquid Systems (MCS))

decane; membrane

Hanna, Gregory J.; Noble, Richard D.; Michael, Frederick C.; Journal of Physical Chemistry; vol. 91; nb. 2; (1987); p. 362 - 365, View in Reaxys 67 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

between water and nitrobenzene-toluene mixture

Hegazi, Mohamed M. Fahmi; Bulletin of the Chemical Society of Japan; vol. 59; (1986); p. 3945 - 3950, View in Reaxys 68 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

between water and nitrobenzene

Hegazi, Mohamed M. Fahmi; Bulletin of the Chemical Society of Japan; vol. 59; (1986); p. 3945 - 3950, View in Reaxys 69 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

between water and toluene

Hegazi, Mohamed M. Fahmi; Bulletin of the Chemical Society of Japan; vol. 59; (1986); p. 3945 - 3950, View in Reaxys 70 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

between water (containing NaCl and HCl) and cyclohexane

Hegazi, Mohamed M. Fahmi; Bulletin of the Chemical Society of Japan; vol. 59; (1986); p. 3945 - 3950, View in Reaxys 71 of 160

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

-3

Partner (Liquid/Liquid Systems (MCS))

H2O

Kaatze; Woermann; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 86; nb. 1; (1982); p. 81 - 87, View in Reaxys

138/428

2017-08-01 04:43:04

72 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O

Partner (Liquid/Liquid Systems (MCS))

benzene

Korenman, Ya. I.; Sel'manshchuk, N. N.; Russian Journal of Physical Chemistry; vol. 56; nb. 4; (1982); p. 558 560; Zhurnal Fizicheskoi Khimii; vol. 56; nb. 4; (1982); p. 920 - 923, View in Reaxys 73 of 160

Description (Liquid/ Liquid Systems (MCS))

Temperature of separation

Partner (Liquid/Liquid Systems (MCS))

D2O

Gansen; Janssen; Schoen; Woermann; Schoenert; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 84; nb. 11; (1980); p. 1149 - 1156, View in Reaxys 74 of 160

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Partner (Liquid/Liquid Systems (MCS))

D2O

Gansen; Janssen; Schoen; Woermann; Schoenert; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 84; nb. 11; (1980); p. 1149 - 1156, View in Reaxys 75 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Rekker; Kort; European Journal of Medicinal Chemistry; vol. 14; (1979); p. 479,484, View in Reaxys; Johansson; Gustavii; Acta Pharmaceutica Suecica; vol. 13; (1976); p. 407,411, View in Reaxys; Vignes; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 57; (1960); p. 966,978, View in Reaxys; Christensen; Acta Chemica Scandinavica (1947-1973); vol. 16; (1962); p. 2363,2365, View in Reaxys; Kusnezow et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 34; (1961); p. 1829,1735; Chem.Abstr.; nb. 3318; (1962), View in Reaxys; Chifu; Albu; Annali di Chimica (Rome, Italy); vol. 65; (1975); p. 519, View in Reaxys; Heric et al.; Journal of Chemical and Engineering Data; vol. 11; (1966); p. 38, View in Reaxys; England; Berg; AIChE Journal; vol. 17; (1971); p. 313,319, View in Reaxys; Desai; Eisen; Journal of Chemical and Engineering Data; vol. 16; (1971); p. 200,201, View in Reaxys; Sekine et al.; Bulletin of the Chemical Society of Japan; vol. 40; (1967); p. 27,29, View in Reaxys; Hansch et al.; Journal of Organic Chemistry; vol. 37; (1972); p. 3090, View in Reaxys; Korenman et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 47; (1974); p. 2075,2130, View in Reaxys; Rubio et al.; Anales de Quimica (1968-1979); vol. 74; (1978); p. 1434,1435, 1436, 1438, View in Reaxys; Aveyard; Mitchell; Transactions of the Faraday Society; vol. 66; (1970); p. 37,39, View in Reaxys; Korenman; Gur'ev; J. Anal. Chem. USSR (Engl. Transl.); vol. 30; (1975); p. 1601, View in Reaxys; Pyatnitskii et al.; J. Anal. Chem. USSR (Engl. Transl.); vol. 26; (1971); p. 683,593, View in Reaxys; Kojima et al.; Journal of Inorganic and Nuclear Chemistry; vol. 32; (1970); p. 987,989, View in Reaxys; Korenman et al.; Russian Journal of Physical Chemistry; vol. 47; (1973); p. 682; ; p. 1207, View in Reaxys; Fujii; Tanaka; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 73; (1977); p. 788,790, 793, View in Reaxys; Kuznetsova; Gurarii; Russian Journal of Inorganic Chemistry (Translation of Zhurnal Neorganicheskoi Khimii); vol. 45; (1971); p. 1761, View in Reaxys; Beckett; Moffat; The Journal of pharmacy and pharmacology; vol. 21; (1969); p. Suppl:144S+, View in Reaxys; Niitsu; Sekine; Bulletin of the Chemical Society of Japan; vol. 51; (1978); p. 705,708, View in Reaxys; Levitanaite et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 43; (1970); p. 115,107, View in Reaxys; Heinonen; Tommila; Suomen Kemistilehti B; vol. 42; (1969); p. 113, View in Reaxys 76 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Krupatkin; Rozhentsova; Russian Journal of Physical Chemistry; vol. 44; (1970); p. 575; ; p. 1036, View in Reaxys; Chandy; Rao; Journal of Chemical and Engineering Data; vol. 7; (1962); p. 473, View in Reaxys; Aleksandrova et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 46; (1973); p. 210,219, View in Reaxys; Zhuravleva; Russian Journal of Physical Chemistry; vol. 51; (1977); p. 596; ; p. 1002, View in Reaxys 77 of 160

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

Mirada Lillo; Gonzalez Trigo; Anales de la Real Sociedad Espanola de Fisica y Quimica, Serie B: Quimica; vol. 56; (1960); p. 217, View in Reaxys 78 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

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Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

Zusammensetzung der fluessigen Phasen.

Partner (Liquid/Liquid Systems (MCS))

water; ethyl acetate

Yuean; Chang; Acta folica sinica; vol. 4; nb. 2; (1959); p. 164,165; Chem.Abstr.; (1960); p. 7271, View in Reaxys 79 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

Zusammensetzung der fluessigen Phasen.

Partner (Liquid/Liquid Systems (MCS))

water; ethyl acetate

Yuean; Chang; Acta folica sinica; vol. 4; nb. 2; (1959); p. 164,165; Chem.Abstr.; (1960); p. 7271, View in Reaxys 80 of 160

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Partner (Liquid/Liquid Systems (MCS))

water; sodium chloride

White et al.; Transactions of the Faraday Society; vol. 54; (1958); p. 1638,1641, View in Reaxys 81 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

Zusammensetzung der fluessigen Phasen.

Partner (Liquid/Liquid Systems (MCS))

water; Methyl isobutyl carbinol

Rao et al.; Chemical Engineering Science; vol. 8; (1958); p. 265,266, View in Reaxys 82 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; 4-methyl-pentan-2-one

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Bak; Geankoplis; Journal of Chemical and Engineering Data; vol. 3; (1958); p. 256, View in Reaxys 83 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

Zusammensetzung der fluessigen Phasen.

Partner (Liquid/Liquid Systems (MCS))

water; benzoic acid ethyl ester

Rao; Rao; Journal of Scientific and Industrial Research; vol. 16 B; (1957); p. 102, View in Reaxys 84 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

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Temperature (Liquid/ Liquid Systems (MCS)) [°C]

0 - 40

Comment (Liquid/Liquid Systems (MCS))

Zusammensetzung der fluessigen Phasen.

Partner (Liquid/Liquid Systems (MCS))

water; N-methylaniline

Angelescu; Hoelszky; Anal.Univ.Bukarest; nb. 12; (1956); p. 77,78,80,81,83,84; Chem.Abstr.; (1958); p. 19896, View in Reaxys 85 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

0 - 40

Comment (Liquid/Liquid Systems (MCS))

Zusammensetzung der fluessigen Phasen.

Partner (Liquid/Liquid Systems (MCS))

water; N,N-dimethyl-aniline

Angelescu; Hoelszky; Anal.Univ.Bukarest; nb. 12; (1956); p. 77,78,80,81,83,84; Chem.Abstr.; (1958); p. 19896, View in Reaxys 86 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

0 - 40

Comment (Liquid/Liquid Systems (MCS))

Zusammensetzung der fluessigen Phasen.

Partner (Liquid/Liquid Systems (MCS))

water; N-ethyl-N-phenylamine

Angelescu; Hoelszky; Anal.Univ.Bukarest; nb. 12; (1956); p. 77,78,80,81,83,84; Chem.Abstr.; (1958); p. 19896, View in Reaxys 87 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

0 - 40

Comment (Liquid/Liquid Systems (MCS))

Zusammensetzung der fluessigen Phasen.

Partner (Liquid/Liquid Systems (MCS))

water; N,N-diethylaniline

Angelescu; Hoelszky; Anal.Univ.Bukarest; nb. 12; (1956); p. 77,78,80,81,83,84; Chem.Abstr.; (1958); p. 19896, View in Reaxys 88 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; benzene

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

6.3

Davies; Griffith; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 6; (1956); p. 143, View in Reaxys 89 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

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Temperature (Liquid/ Liquid Systems (MCS)) [°C]

32.5

Comment (Liquid/Liquid Systems (MCS))

Zusammensetzung der fluessigen Phasen.

Partner (Liquid/Liquid Systems (MCS))

water; Trichloroethylene

Krishnamurty; Rao; Trans.Indian Inst.chem.Eng.; vol. 8; (1955); p. 52, View in Reaxys 90 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

Zusammensetzung der fluessigen Phasen.

Partner (Liquid/Liquid Systems (MCS))

water; benzene

Krishnamurty; Rao; Trans.Indian Inst.chem.Eng.; vol. 8; (1955); p. 52, View in Reaxys 91 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

Zusammensetzung der fluessigen Phasen.

Partner (Liquid/Liquid Systems (MCS))

water; acetic acid butyl ester

Rao et al.; Trans.Indian Inst.chem.Eng.; vol. 8; (1955); p. 46, View in Reaxys 92 of 160

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Rao et al.; Transactions, Indian Institute of Chemical Engineers; vol. 8; (1955); p. 46; Chem.Abstr.; nb. 14397; (1957), View in Reaxys; Krishnamurty; Venkatarao; Transactions, Indian Institute of Chemical Engineers; vol. 8; (1955); p. 52; Chem.Abstr.; nb. 14399; (1957), View in Reaxys 93 of 160

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

Zusammensetzung der fluessigen Phasen.

Partner (Liquid/Liquid Systems (MCS))

water; diphenylether

Purnell; Bowden; Journal of the Chemical Society; (1954); p. 539,542,543,544, View in Reaxys 94 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; CCl4

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

20 - 30

Bhat et al.; Canad.J.Technol.; vol. 32; (1954); p. 151, View in Reaxys 95 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

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Solvent (Liquid/Liquid Systems (MCS))

H2O; toluene

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Smith; White; Journal of Physical Chemistry; vol. 33; (1929); p. 1958, View in Reaxys; Ward; Brooks; Transactions of the Faraday Society; vol. 48; (1952); p. 1124, View in Reaxys 96 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; toluene

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Ward; Brooks; Transactions of the Faraday Society; vol. 48; (1952); p. 1124, View in Reaxys 97 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; octan-1-ol

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Collander; Acta Chemica Scandinavica (1947-1973); vol. 5; (1951); p. 774,775, View in Reaxys 98 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; 2-methyl-propan-1-ol

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Collander; Acta Chemica Scandinavica (1947-1973); vol. 4; (1950); p. 1085,1089, View in Reaxys 99 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; CHCl3

Marvel; Richards; Analytical Chemistry; vol. 21; (1949); p. 1481, View in Reaxys 100 of 160 Description (Liquid/ Liquid Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

Distribution between solvent 1 + 2 H2O; ethyl acetate

Marvel; Richards; Analytical Chemistry; vol. 21; (1949); p. 1481, View in Reaxys 101 of 160 Description (Liquid/ Liquid Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

Distribution between solvent 1 + 2 H2O; butan-1-ol

Archibald; Journal of the American Chemical Society; vol. 54; (1932); p. 3180, View in Reaxys; Marvel; Richards; Analytical Chemistry; vol. 21; (1949); p. 1481, View in Reaxys 102 of 160 Description (Liquid/ Liquid Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

Distribution between solvent 1 + 2 H2O; diethyl ether

Dermer; Dermer; Journal of the American Chemical Society; vol. 65; (1943); p. 1654, View in Reaxys; Damkoehler; Eggersgluess; Zeitschrift fuer Physikalische Chemie, Abteilung B: Chemie der Elementarprozesse, Aufbau der

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Materie; vol. 51; (1942); p. 166, View in Reaxys; Marvel; Richards; Analytical Chemistry; vol. 21; (1949); p. 1481, View in Reaxys; Osburn,Wood,Werkman; Industrial and Engineering Chemistry, Analytical Edition; vol. 5; (1933); p. 249; Industrial and Engineering Chemistry, Analytical Edition; vol. 8; (1936); p. 272, View in Reaxys 103 of 160 Description (Liquid/ Liquid Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

Distribution between solvent 1 + 2 H2O; tributyl phosphate

Pagel; McLafferty; Analytical Chemistry; vol. 20; (1948); p. 272, View in Reaxys 104 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; 1,2,3,4-tetrahydro-naphthalene

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Patent; Standard Oil Devel.Co.; US2537658; (1948), View in Reaxys 105 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; 1,2,3,4-tetrahydro-naphthalene

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Patent; Standard Oil Devel.Co.; US2537658; (1948), View in Reaxys 106 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; 2-methyl-phenol

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Patent; Standard Oil Devel.Co.; US2537658; (1948), View in Reaxys 107 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; 2-methyl-phenol

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Patent; Standard Oil Devel.Co.; US2537658; (1948), View in Reaxys 108 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; 3,5,5-trimethyl-cyclohex-2-enone

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Patent; Standard Oil Devel.Co.; US2537658; (1948), View in Reaxys 109 of 160 Description (Liquid/ Liquid Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

Distribution between solvent 1 + 2 H2O; 3,5,5-trimethyl-cyclohex-2-enone

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Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Patent; Standard Oil Devel.Co.; US2537658; (1948), View in Reaxys 110 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; 3,5,5-trimethyl-cyclohex-2-enone

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

125

Patent; Standard Oil Devel.Co.; US2537658; (1948), View in Reaxys 111 of 160

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

0 - 40

Comment (Liquid/Liquid Systems (MCS))

Zustandsdiagramm des ternaeren Systems mit Wasser und Anilin bei 0grad, 20grad und 40grad:.

Partner (Liquid/Liquid Systems (MCS))

water; aniline

Angelescu; Cristodulo; Bulet.; vol. 3A; (1941); p. 32; Chem. Zentralbl.; vol. 114; nb. II; (1943); p. 2233, View in Reaxys; Angelescu; Cristodulo; Bulet.; vol. <2>2; (1940); p. 114; Chem. Zentralbl.; vol. 113; nb. II; (1942); p. 1675, View in Reaxys 112 of 160

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

0 - 40

Comment (Liquid/Liquid Systems (MCS))

Zustandsdiagramm des ternaeren Systems mit Wasser und o-Toluidin bei 0grad, 20grad und 40grad:.

Partner (Liquid/Liquid Systems (MCS))

water; o-toluidine

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

0 - 40

Comment (Liquid/Liquid Systems (MCS))

Zustandsdiagramm des ternaeren Systems mit Wasser und m-Toluidin bei 0grad, 20grad und 40grad:.

Partner (Liquid/Liquid Systems (MCS))

water; 1-amino-3-methylbenzene

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

Zustandsdiagramm des ternaeren Systems mit Wasser und NaCl bei 25grad:.

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Partner (Liquid/Liquid Systems (MCS))

water; NaCl

Bury; Mends; Journal of the Chemical Society; (1939); p. 742, View in Reaxys 115 of 160

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; benzene

Comment (Liquid/Liquid Systems (MCS))

bei verschiedenen Temperaturen.

Bekturow; Zhurnal Obshchei Khimii; vol. 9; (1939); p. 1719,1720; Chem. Zentralbl.; vol. 112; nb. I; (1941); p. 2513, View in Reaxys 116 of 160

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

Zustandsdiagramm des ternaeren Systems mit Wasser und CCl4 bei 25grad:.

Partner (Liquid/Liquid Systems (MCS))

water; tetrachloromethane

Smith; Berman; Journal of the American Chemical Society; vol. 59; (1937); p. 2390, View in Reaxys 117 of 160

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

ethanol; NaCl

Schlesinger; Kirejew; Zhurnal Obshchei Khimii; vol. 7; (1937); p. 2342; Chem. Zentralbl.; vol. 109; nb. I; (1938); p. 3762, View in Reaxys 118 of 160

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

ethanol; KCl

Schlesinger; Kirejew; Zhurnal Obshchei Khimii; vol. 7; (1937); p. 2342; Chem. Zentralbl.; vol. 109; nb. I; (1938); p. 3762, View in Reaxys 119 of 160

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

ethanol; CaCl2

Schlesinger; Kirejew; Zhurnal Obshchei Khimii; vol. 7; (1937); p. 2342; Chem. Zentralbl.; vol. 109; nb. I; (1938); p. 3762, View in Reaxys 120 of 160 Description (Liquid/ Liquid Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Solution equilibrium 100

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Partner (Liquid/Liquid Systems (MCS))

ethanol; NaCl

Schlesinger; Kirejew; Zhurnal Obshchei Khimii; vol. 7; (1937); p. 2342; Chem. Zentralbl.; vol. 109; nb. I; (1938); p. 3762, View in Reaxys 121 of 160 Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

100

Partner (Liquid/Liquid Systems (MCS))

ethanol; KCl

Schlesinger; Kirejew; Zhurnal Obshchei Khimii; vol. 7; (1937); p. 2342; Chem. Zentralbl.; vol. 109; nb. I; (1938); p. 3762, View in Reaxys 122 of 160 Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

100

Partner (Liquid/Liquid Systems (MCS))

ethanol; CaCl2

Schlesinger; Kirejew; Zhurnal Obshchei Khimii; vol. 7; (1937); p. 2342; Chem. Zentralbl.; vol. 109; nb. I; (1938); p. 3762, View in Reaxys 123 of 160 Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

180

Partner (Liquid/Liquid Systems (MCS))

ethanol; NaCl

Schlesinger; Kirejew; Zhurnal Obshchei Khimii; vol. 7; (1937); p. 2342; Chem. Zentralbl.; vol. 109; nb. I; (1938); p. 3762, View in Reaxys 124 of 160 Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

180

Partner (Liquid/Liquid Systems (MCS))

ethanol; KCl; CaCl2

Schlesinger; Kirejew; Zhurnal Obshchei Khimii; vol. 7; (1937); p. 2342; Chem. Zentralbl.; vol. 109; nb. I; (1938); p. 3762, View in Reaxys 125 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; benzene

Comment (Liquid/Liquid Systems (MCS))

Einfluss einiger Alkohole auf die Verteilung.

Sym; Biochemical Journal; vol. 30; (1936); p. 613; Enzymol.; vol. 2; (1937); p. 108; Chem. Zentralbl.; vol. 108; nb. II; (1937); p. 2020, View in Reaxys 126 of 160 Description (Liquid/ Liquid Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Solution equilibrium 25

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Comment (Liquid/Liquid Systems (MCS))

Zustandsdiagramm des ternaeren Systems mit Wasser und NaOH bei 25grad:.

Partner (Liquid/Liquid Systems (MCS))

water; tetrachloromethane

Bury; Owens; Transactions of the Faraday Society; vol. 31; (1935); p. 480, View in Reaxys 127 of 160 Description (Liquid/ Liquid Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

Distribution between solvent 1 + 2 H2O; CCl4

Kolossowski; Kulikow; Bekturow; Bulletin de la Societe Chimique de France; vol. <5>2; (1935); p. 464, View in Reaxys; Kolossowski; Kulikow; Bekturow; Zhurnal Obshchei Khimii; vol. 4; (1934); p. 1231,1372; Zhurnal Obshchei Khimii; vol. 5; (1935); p. 321, View in Reaxys 128 of 160 Description (Liquid/ Liquid Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

Distribution between solvent 1 + 2 H2O; nitrobenzene

Kolossowski; Kulikow; Bekturow; Bulletin de la Societe Chimique de France; vol. <5>2; (1935); p. 464, View in Reaxys; Kolossowski; Kulikow; Bekturow; Zhurnal Obshchei Khimii; vol. 4; (1934); p. 1231,1372; Zhurnal Obshchei Khimii; vol. 5; (1935); p. 321, View in Reaxys 129 of 160 Description (Liquid/ Liquid Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

Distribution between solvent 1 + 2 H2O; 2-nitro-toluene

Kolossowski; Kulikow; Bekturow; Bulletin de la Societe Chimique de France; vol. <5>2; (1935); p. 464, View in Reaxys; Kolossowski; Kulikow; Bekturow; Zhurnal Obshchei Khimii; vol. 4; (1934); p. 1231,1372; Zhurnal Obshchei Khimii; vol. 5; (1935); p. 321, View in Reaxys 130 of 160 Description (Liquid/ Liquid Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

Distribution between solvent 1 + 2 H2O; 2-methyl-propan-1-ol

Kolossowski; Kulikow; Bekturow; Bulletin de la Societe Chimique de France; vol. <5>2; (1935); p. 464, View in Reaxys; Kolossowski; Kulikow; Bekturow; Zhurnal Obshchei Khimii; vol. 4; (1934); p. 1231,1372; Zhurnal Obshchei Khimii; vol. 5; (1935); p. 321, View in Reaxys 131 of 160 Description (Liquid/ Liquid Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

Distribution between solvent 1 + 2 H2O

Archibald; Journal of the American Chemical Society; vol. 54; (1932); p. 3180, View in Reaxys; Kolossowski; Kulikow; Bekturow; Bulletin de la Societe Chimique de France; vol. <5>2; (1935); p. 464, View in Reaxys; Kolossowski; Kulikow; Bekturow; Zhurnal Obshchei Khimii; vol. 4; (1934); p. 1231,1372; Zhurnal Obshchei Khimii; vol. 5; (1935); p. 321, View in Reaxys 132 of 160 Description (Liquid/ Liquid Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

Distribution between solvent 1 + 2 H2O; toluene

Kolossowski; Ponomarewa; Bulletin de la Societe Chimique de France; vol. <5>1; (1934); p. 66; Zhurnal Obshchei Khimii; vol. 4; (1934); p. 1065, View in Reaxys 133 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

2,2,4-trimethyl-pentane; 2-methoxy-ethanol

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

148/428

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Henriques; Journal of the American Chemical Society; vol. 55; (1933); p. 3285, View in Reaxys 134 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

2,2,4-trimethyl-pentane; 2-methoxy-ethanol

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

-19.5

Henriques; Journal of the American Chemical Society; vol. 55; (1933); p. 3285, View in Reaxys 135 of 160 Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Solvent (Liquid/Liquid Systems (MCS))

H2O

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

-4.1

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys 136 of 160 Description (Liquid/ Liquid Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

Distribution between solvent 1 + 2 H2O; petroleum ether

Grossfeld; Miermeister; Zeitschrift fuer Analytische Chemie; vol. 87; (1932); p. 242, View in Reaxys 137 of 160 Description (Liquid/ Liquid Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

Distribution between solvent 1 + 2 benzene

Angelescu; Dutchievici; Bulet.Soc.Chim.Romania; vol. 14; (1932); p. 48; Chem. Zentralbl.; vol. 104; nb. I; (1933); p. 3271, View in Reaxys 138 of 160 Description (Liquid/ Liquid Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

Distribution between solvent 1 + 2 H2O; butan-2-ol

Archibald; Journal of the American Chemical Society; vol. 54; (1932); p. 3180, View in Reaxys 139 of 160 Description (Liquid/ Liquid Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

Distribution between solvent 1 + 2 H2O; butan-2-one

Archibald; Journal of the American Chemical Society; vol. 54; (1932); p. 3180, View in Reaxys 140 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; olive oil

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Bodansky; Meigs; Journal of Physical Chemistry; vol. 36; (1932); p. 816, View in Reaxys 141 of 160 Description (Liquid/ Liquid Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

Distribution between solvent 1 + 2 H2O; olive oil

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Temperature (Liquid/ Liquid Systems (MCS)) [°C]

37.5

Bodansky; Meigs; Journal of Physical Chemistry; vol. 36; (1932); p. 816, View in Reaxys 142 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

2,2,4-trimethyl-pentane; methanol

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Smith; Norton; Journal of the American Chemical Society; vol. 54; (1932); p. 3812, View in Reaxys 143 of 160 Description (Liquid/ Liquid Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

Distribution between solvent 1 + 2 H2O; benzene

Keane; Narracott; Chem. Zentralbl.; vol. 80; nb. II; (1909); p. 2135, View in Reaxys; v.Georgievics; Monatshefte fuer Chemie; vol. 34; (1913); p. 1857; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 84; (1913); p. 358, View in Reaxys; Angelescu; Dutchievici; Bulet.Soc.Chim.Romania; vol. 14; (1932); p. 48; Chem. Zentralbl.; vol. 104; nb. I; (1933); p. 3271, View in Reaxys 144 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; diisopropyl ether

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Werkman; Industrial and Engineering Chemistry, Analytical Edition; vol. 2; (1930); p. 302; Iowa State College Journal of Science; vol. 5; (1930); p. 122, View in Reaxys 145 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; CHCl3

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Smith; Journal of Physical Chemistry; vol. 25; (1921); p. 231; Journal of Physical Chemistry; vol. 26; (1922); p. 269,270, View in Reaxys; Smith; White; Journal of Physical Chemistry; vol. 33; (1929); p. 1967, View in Reaxys 146 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; benzene

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Brown; Bury; Journal of the Chemical Society; vol. 123; (1923); p. 2431,2432, View in Reaxys; Smith; White; Journal of Physical Chemistry; vol. 33; (1929); p. 1967, View in Reaxys 147 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; olive oil

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

150/428

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Bodansky; Journal of Biological Chemistry; vol. 79; (1928); p. 252, View in Reaxys 148 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; hexane

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Harkins; McLaughlin; Journal of the American Chemical Society; vol. 47; (1925); p. 1612, View in Reaxys; Rehbinder; Biochemische Zeitschrift; vol. 187; (1927); p. 23, View in Reaxys 149 of 160 Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

-1.2 - -1

Partner (Liquid/Liquid Systems (MCS))

water

Howard; Patterson; Journal of the Chemical Society; (1926); p. 2792, View in Reaxys 150 of 160 Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Comment (Liquid/Liquid Systems (MCS))

Einfluss von Chromsalzen.

Partner (Liquid/Liquid Systems (MCS))

water

Howard; Patterson; Journal of the Chemical Society; (1926); p. 2792, View in Reaxys 151 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; diethyl ether

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Behrens; Fresenius' Zeitschrift fuer Analytische Chemie; vol. 69; (1926); p. 100,101,102, View in Reaxys 152 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; diethyl ether

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Behrens; Fresenius' Zeitschrift fuer Analytische Chemie; vol. 69; (1926); p. 100,101,102, View in Reaxys 153 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; benzene

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Schulz; Koll.Beih.; vol. 21; p. 43,46; Chem. Zentralbl.; vol. 96; nb. II; (1925); p. 1840, View in Reaxys 154 of 160 Description (Liquid/ Liquid Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

Distribution between solvent 1 + 2 H2O; diethyl ether

151/428

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Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Smith; Journal of Physical Chemistry; vol. 25; (1921); p. 622, View in Reaxys; Johnson; Cereal Chem.; vol. 2; (1925); p. 351, View in Reaxys 155 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; CS2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Schulz; Koll.Beih.; vol. 21; p. 51; Chem. Zentralbl.; vol. 96; nb. II; (1925); p. 1840, View in Reaxys 156 of 160 Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

-0.8

Partner (Liquid/Liquid Systems (MCS))

water

Klein; Lotos; vol. 71; (1923); p. 280, View in Reaxys 157 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Gordon; Reid; Journal of Physical Chemistry; vol. 26; (1922); p. 786, View in Reaxys 158 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; xylene

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Smith; Journal of Physical Chemistry; vol. 25; (1921); p. 231; Journal of Physical Chemistry; vol. 26; (1922); p. 269,270, View in Reaxys 159 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

glycerol; acetone

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Smith; Journal of Physical Chemistry; vol. 25; (1921); p. 732, View in Reaxys 160 of 160 Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O; benzene

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

152/428

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Harkins; King; Journal of the American Chemical Society; vol. 41; (1919); p. 984, View in Reaxys Liquid/Solid Systems (MCS) (14) 1 of 14

Description (Liquid/Solid Eutectic Systems (MCS)) Susarev et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 48; (1975); p. 2575,2664, View in Reaxys

2 of 14

Description (Liquid/Solid Solidification points of mixtures Systems (MCS)) Sumarokowa et al.; Zhurnal Fizicheskoi Khimii; vol. 34; (1960); p. 2727,2728; engl. Ausgabe; p. 1283, View in Reaxys

3 of 14

Description (Liquid/Solid Melting diagram Systems (MCS)) Comment (Liquid/Solid Systems (MCS))

Verbindung 1:1.

Partner (Liquid/Solid Systems (MCS))

p,p'-diaminobiphenyl

Arestenko; Bergman; Zhurnal Obshchei Khimii; vol. 29; (1959); p. 1744;engl.Ausg.S.1721, View in Reaxys 4 of 14

Description (Liquid/Solid Melting diagram Systems (MCS)) Partner (Liquid/Solid Systems (MCS))

phenyl carbamate

Rudenko et al.; Zhurnal Obshchei Khimii; vol. 27; (1957); p. 2030,2031;engl.Ausg.S.2084, View in Reaxys 5 of 14

Description (Liquid/Solid Melting diagram Systems (MCS)) Partner (Liquid/Solid Systems (MCS))

water

Kusnezowa; Bergmann; Zhurnal Obshchei Khimii; vol. 26; (1956); p. 1326,1329; engl. Ausg. S. 1497, 1498, View in Reaxys 6 of 14

Description (Liquid/Solid Solidification diagram Systems (MCS)) Partner (Liquid/Solid Systems (MCS))

water; urea

Kusnezowa; Bergmann; Zhurnal Obshchei Khimii; vol. 26; (1956); p. 1326,1329; engl. Ausg. S. 1497, 1498, View in Reaxys 7 of 14

Description (Liquid/Solid Melting diagram Systems (MCS)) Comment (Liquid/Solid Systems (MCS))

Verbindung 1:1.

Partner (Liquid/Solid Systems (MCS))

acetamide

Rudenko et al.; Zhurnal Obshchei Khimii; vol. 25; (1955); p. 2430,2432;engl.Ausg.S.2311, View in Reaxys 8 of 14

Description (Liquid/Solid Melting diagram Systems (MCS)) Comment (Liquid/Solid Systems (MCS))

Verbindungen 4:1 und 2:1.

Partner (Liquid/Solid Systems (MCS))

ethylenediamine

Bergman; Koloskowa; Izv.Sektora fiz.chim.Anal.; vol. 22; (1953); p. 337,344; Chem.Abstr.; (1957); p. 14609, View in Reaxys 9 of 14

Description (Liquid/Solid Eutectic Systems (MCS))

153/428

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Temperature (Liquid/ Solid Systems (MCS)) [°C]

-23.4

Comment (Liquid/Solid Systems (MCS))

17prozent Buttersaeure; Additionsverbindung 1:1 (F:50.2grad).

Partner (Liquid/Solid Systems (MCS))

hydrazine

Ssemischin; Zhurnal Obshchei Khimii; vol. 13; (1943); p. 633,634; Chem.Abstr.; (1945); p. 456, View in Reaxys 10 of 14

Description (Liquid/Solid Eutectic Systems (MCS)) Temperature (Liquid/ Solid Systems (MCS)) [°C]

-18.9

Comment (Liquid/Solid Systems (MCS))

82 Mol.-prozent Buttersaeure.

Partner (Liquid/Solid Systems (MCS))

urea

Bergman; Kusnetzowa; Zhurnal Obshchei Khimii; vol. 9; (1939); p. 633,634; Chem. Zentralbl.; vol. 112; nb. I; (1941); p. 634, View in Reaxys 11 of 14

Description (Liquid/Solid Eutectic Systems (MCS)) Temperature (Liquid/ Solid Systems (MCS)) [°C]

-26

Comment (Liquid/Solid Systems (MCS))

71.2 Mol.-prozent Buttersaeure; Auftreten von NaC4H7O2+C4H8O2 und einer weiteren unbestaendigen Additionsverbindung.

Partner (Liquid/Solid Systems (MCS))

sodium butyrate

Bakunin; Vitale; Gazzetta Chimica Italiana; vol. 65; (1935); p. 593,598, 600, 603, 604, View in Reaxys 12 of 14

Description (Liquid/Solid Eutectic Systems (MCS)) Temperature (Liquid/ Solid Systems (MCS)) [°C]

-35

Comment (Liquid/Solid Systems (MCS))

67 Gew.-prozent Buttersaeure.

Partner (Liquid/Solid Systems (MCS))

acetic acid

Bhatt; Watson; Journal of the Indian Institute of Science, Section A; vol. 13; (1930); p. 143,145, View in Reaxys 13 of 14

Description (Liquid/Solid Eutectic Systems (MCS)) Temperature (Liquid/ Solid Systems (MCS)) [°C]

-10.4

Partner (Liquid/Solid Systems (MCS))

water

Ballo; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 72; (1910); p. 445, View in Reaxys 14 of 14

Description (Liquid/Solid Eutectic Systems (MCS)) Temperature (Liquid/ Solid Systems (MCS)) [°C]

-13.4

154/428

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Partner (Liquid/Solid Systems (MCS))

water

Faucon; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 148; (1909); p. 1189; Annales de Chimie (Cachan, France); vol. <8>19; (1910); p. 96, View in Reaxys Liquid/Vapour Systems (MCS) (53) 1 of 53

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

water; pyridine

Cherkasov; Smotrov; Il'in; Russian Journal of Applied Chemistry; vol. 81; nb. 2; (2008); p. 218 - 222, View in Reaxys 2 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 100 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

propionic acid

Giles, Neil F.; Wilson, Grant M.; Journal of Chemical and Engineering Data; vol. 51; nb. 6; (2006); p. 1966 - 1972, View in Reaxys 3 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 140 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

propionic acid

Giles, Neil F.; Wilson, Grant M.; Journal of Chemical and Engineering Data; vol. 51; nb. 6; (2006); p. 1966 - 1972, View in Reaxys 4 of 53

Description (Liquid/ Liquid/vapour phase diagram Vapour Systems (MCS)) Temperature (Liquid/ 100 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

propionic acid

Giles, Neil F.; Wilson, Grant M.; Journal of Chemical and Engineering Data; vol. 51; nb. 6; (2006); p. 1966 - 1972, View in Reaxys 5 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 100 - 140 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

propionic acid

Giles, Neil F.; Wilson, Grant M.; Journal of Chemical and Engineering Data; vol. 51; nb. 6; (2006); p. 1966 - 1972, View in Reaxys 6 of 53

Description (Liquid/ Fugacities Vapour Systems (MCS)) Temperature (Liquid/ 100 - 140 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

propionic acid

155/428

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Giles, Neil F.; Wilson, Grant M.; Journal of Chemical and Engineering Data; vol. 51; nb. 6; (2006); p. 1966 - 1972, View in Reaxys 7 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 88.17 - 110.25 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 105.008 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

propionic acid

Sewnarain, Reshan; Ramjugernath, Deresh; Raal, J. David; Journal of Chemical and Engineering Data; vol. 47; nb. 3; (2002); p. 603 - 607, View in Reaxys 8 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 110.25 - 123.03 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 105.008 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

isovaleric acid

Sewnarain, Reshan; Ramjugernath, Deresh; Raal, J. David; Journal of Chemical and Engineering Data; vol. 47; nb. 3; (2002); p. 603 - 607, View in Reaxys 9 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 88.3 - 140.5 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 199.891 - 400.007 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

butan-1-ol

Munoz, Laura A. L.; Kraehenbuehl, M. Alvina; Journal of Chemical and Engineering Data; vol. 46; nb. 1; (2001); p. 120 - 124, View in Reaxys 10 of 53

Description (Liquid/ Liquid/vapour phase diagram Vapour Systems (MCS)) Temperature (Liquid/ 88.3 - 140.5 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 199.891 - 400.007 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

butan-1-ol

Munoz, Laura A. L.; Kraehenbuehl, M. Alvina; Journal of Chemical and Engineering Data; vol. 46; nb. 1; (2001); p. 120 - 124, View in Reaxys 11 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 80.3 - 104.4 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 199.891 - 400.007 Systems (MCS)) [Torr]

156/428

2017-08-01 04:43:04

Partner (Liquid/Vapour Systems (MCS))

acetic acid

Munoz, Laura A. L.; Kraehenbuehl, M. Alvina; Journal of Chemical and Engineering Data; vol. 46; nb. 1; (2001); p. 120 - 124, View in Reaxys 12 of 53

Description (Liquid/ Liquid/vapour phase diagram Vapour Systems (MCS)) Temperature (Liquid/ 80.3 - 104.3 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 199.891 - 400.007 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

acetic acid

Munoz, Laura A. L.; Kraehenbuehl, M. Alvina; Journal of Chemical and Engineering Data; vol. 46; nb. 1; (2001); p. 120 - 124, View in Reaxys 13 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 85.05 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 36.0029 - 94.5076 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

propionic acid

Iwai; Miyamoto; Arai; Nakamura; Journal of Chemical and Engineering Data; vol. 46; nb. 2; (2001); p. 405 - 409, View in Reaxys 14 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 85.05 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 37.503 - 255.77 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

acetic acid

Iwai; Miyamoto; Arai; Nakamura; Journal of Chemical and Engineering Data; vol. 46; nb. 2; (2001); p. 405 - 409, View in Reaxys 15 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 85.05 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

propionic acid; acetic acid

Miyamoto, Shinji; Nakamura, Shinichi; Iwai, Yoshio; Arai, Yasuhiko; Journal of Chemical and Engineering Data; vol. 46; nb. 5; (2001); p. 1225 - 1230, View in Reaxys 16 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 120 - 155.1 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 70.1306 - 574.621 Systems (MCS)) [Torr]

157/428

2017-08-01 04:43:04

Partner (Liquid/Vapour Systems (MCS))

butanoic acid anhydride

Zudkevitch; Lindrud; Chu; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 393 - 397, View in Reaxys 17 of 53

Description (Liquid/ Liquid/vapour phase diagram Vapour Systems (MCS)) Temperature (Liquid/ 120 - 155.1 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 70.1306 - 574.621 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

butanoic acid anhydride

Zudkevitch; Lindrud; Chu; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 393 - 397, View in Reaxys 18 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 120 - 155.1 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 70.1306 - 574.621 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

butanoic acid anhydride

Zudkevitch; Lindrud; Chu; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 393 - 397, View in Reaxys 19 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 1.9 - 24.9 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

2-methyl-but-2-ene; tert-Amyl alcohol

Kashkarova, I. B.; Rozhnov, A. M.; Verevkin, S. P.; Russian Journal of Applied Chemistry; vol. 67; nb. 9.1; (1994); p. 1305 - 1308; Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation); vol. 67; nb. 9; (1994); p. 1486 1490, View in Reaxys 20 of 53

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 40 - 60 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

aniline

Ziegra, S.; Becker, P.; Kerber, R.; Kehlen, H.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 270; nb. 6; (1989); p. 1222 - 1225, View in Reaxys 21 of 53

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 40 - 60 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

pyridine

Ziegra, S.; Becker, P.; Kerber, R.; Kehlen, H.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 270; nb. 6; (1989); p. 1222 - 1225, View in Reaxys

158/428

2017-08-01 04:43:04

22 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Solvent (Liquid/Vapour Systems (MCS))

H2O

Temperature (Liquid/ 39.9 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 14701.2 - 147012 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

carbon dioxide

Panaglotopoulos; Willson; Reid; Journal of Chemical and Engineering Data; vol. 33; nb. 3; (1988); p. 321 - 327, View in Reaxys 23 of 53

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

H2O

Kaatze; Woermann; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 86; nb. 1; (1982); p. 81 - 87, View in Reaxys 24 of 53

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Temperature (Liquid/ 19.2 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

D2O

Gansen; Janssen; Schoen; Woermann; Schoenert; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 84; nb. 11; (1980); p. 1149 - 1156, View in Reaxys 25 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Radecki; Kaczmarek; Journal of Chemical and Engineering Data; vol. 20; (1975); p. 378,379,380, View in Reaxys; Radwan; Hanna; Journal of Chemical and Engineering Data; vol. 21; (1976); p. 285,286,287,288, View in Reaxys; Trofimov net al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 42; (1969); p. 2556,2408, View in Reaxys

26 of 53

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Apelblat, Kohler; Journal of Chemical Thermodynamics; vol. 8; (1976); p. 749,751, 752, 754, 755, View in Reaxys; Radecki; Kaczmarek; Journal of Chemical and Engineering Data; vol. 20; (1975); p. 378,379,380, View in Reaxys; Wright; Akhtar; Journal of the Chemical Society [Section] B: Physical Organic; (1970); p. 151,152-153, View in Reaxys

27 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Shain; Prausnitz; AIChE Journal; vol. 10; (1964); p. 766, View in Reaxys; Backlund et al.; Finnish Chemical Letters; (1974); p. 277,278-280, View in Reaxys; Wright; Akhtar; Transactions of the Faraday Society; vol. 66; (1970); p. 990,993, View in Reaxys; Backlund et al.; Acta Chemica Scandinavica (1947-1973); vol. 27; (1973); p. 3234,3240, View in Reaxys

28 of 53

Description (Liquid/ Partial pressures of the components Vapour Systems (MCS)) Amandrut; Bulletin de la Societe Chimique de France; (1972); p. 2228,2230-2232, View in Reaxys

29 of 53

Description (Liquid/ Boiling points of mixtures Vapour Systems (MCS)) Rivenq; Bulletin de la Societe Chimique de France; (1962); p. 1192, View in Reaxys

30 of 53

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS))

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Motscharnjuk; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 1086,1103; Chem.Abstr.; nb. 23624; (1960), View in Reaxys 31 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Pressure (Liquid/Vapour 760 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

acetic acid

Yuean; Chang; Acta focalia sinica; vol. 4; nb. 2; (1959); p. 164,167; Chem.Abstr.; (1960); p. 7271, View in Reaxys 32 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Pressure (Liquid/Vapour 760 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

propionic acid

Yuean; Chang; Acta focalia sinica; vol. 4; nb. 2; (1959); p. 164,167; Chem.Abstr.; (1960); p. 7271, View in Reaxys 33 of 53

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Comment (Liquid/ Temperatur. Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

acetone

Golik; Motscharnjuk; Ukrainskii Khimicheskii Zhurnal (Russian Edition); vol. 24; (1958); p. 33; Chem.Abstr.; (1958); p. 17905, View in Reaxys 34 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Comment (Liquid/ aus Dampfdruckmessungen ermittelt. Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

water

Hansen et al.; Journal of Physical Chemistry; vol. 59; (1955); p. 391,393, View in Reaxys 35 of 53

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Comment (Liquid/ Temperatur. Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

water

Golik et al.; Ukrainskii Khimicheskii Zhurnal (Russian Edition); vol. 21; (1955); p. 480,481; Chem.Abstr.; (1956); p. 4592, View in Reaxys 36 of 53

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Comment (Liquid/ Temperatur. Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

ethanol

Golik et al.; Ukrainskii Khimicheskii Zhurnal (Russian Edition); vol. 21; (1955); p. 318; Chem.Abstr.; (1956); p. 4592, View in Reaxys; Solomko; Sovesc.Stroenie zidkom Sost.Kiew; (1953); p. 97,101; Chem.Abstr.; (1958); p. 841, View in Reaxys 37 of 53

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS))

160/428

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Comment (Liquid/ Temperatur. Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

propan-1-ol

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Comment (Liquid/ Temperatur. Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

butan-1-ol

Description (Liquid/ Partial pressures of the components Vapour Systems (MCS)) Comment (Liquid/ von Buttersaeure ueber Gemischen mit Nitromethan bei 25grad. Vapour Systems (MCS)) Jones; Saunders; Journal of the Chemical Society; (1951); p. 2944,2946,2947, View in Reaxys

40 of 53

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Comment (Liquid/ unter verschiedenen Bedingungen. Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

water

Butler; Ramchandani; Journal of the Chemical Society; (1935); p. 953, View in Reaxys; Othmer; Industrial and Engineering Chemistry; vol. 35; (1943); p. 617, View in Reaxys; Tschernewa; Golbert; Shuchowitzki; Zhurnal Fizicheskoi Khimii; vol. 21; (1947); p. 1403; Chem.Abstr.; (1948); p. 5310, View in Reaxys; Giacalone; Accascina; Carnesi; Gazzetta Chimica Italiana; vol. 72; (1942); p. 113 - 123, View in Reaxys 41 of 53

Description (Liquid/ Partial pressures of the components Vapour Systems (MCS)) Comment (Liquid/ im System mit Wasser unter verschiedenen Bedingungen. Vapour Systems (MCS)) Butler; Ramchandani; Journal of the Chemical Society; (1935); p. 953, View in Reaxys; Othmer; Industrial and Engineering Chemistry; vol. 35; (1943); p. 617, View in Reaxys; Tschernewa; Golbert; Shuchowitzki; Zhurnal Fizicheskoi Khimii; vol. 21; (1947); p. 1403; Chem.Abstr.; (1948); p. 5310, View in Reaxys; Giacalone; Accascina; Carnesi; Gazzetta Chimica Italiana; vol. 72; (1942); p. 113 - 123, View in Reaxys

42 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Comment (Liquid/ unter verschiedenen Bedingungen. Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

water

Description (Liquid/ Boiling points of mixtures Vapour Systems (MCS)) Comment (Liquid/ Destillationskurve. Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

water

161/428

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Knetemann; Recueil des Travaux Chimiques des Pays-Bas; vol. 47; (1928); p. 955, View in Reaxys 44 of 53

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

chloroform

Weissenberger; Henke; Katschinka; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 153; (1926); p. 34, View in Reaxys 45 of 53

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

acetone

Weissenberger; Henke; Katschinka; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 153; (1926); p. 34, View in Reaxys 46 of 53

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

acetic acid methyl ester

Weissenberger; Henke; Katschinka; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 153; (1926); p. 34, View in Reaxys 47 of 53

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

carbon disulfide

Weissenberger; Henke; Katschinka; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 153; (1926); p. 34, View in Reaxys 48 of 53

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

benzene

Weissenberger; Henke; Katschinka; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 153; (1926); p. 34, View in Reaxys 49 of 53

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 0 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

water

Faucon; Annales de Chimie (Cachan, France); vol. <8> 19; (1910); p. 135, View in Reaxys

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50 of 53

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 18.2 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

water

Faucon; Annales de Chimie (Cachan, France); vol. <8> 19; (1910); p. 135, View in Reaxys 51 of 53

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 58.7 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

water

Faucon; Annales de Chimie (Cachan, France); vol. <8> 19; (1910); p. 135, View in Reaxys 52 of 53

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Solvent (Liquid/Vapour Systems (MCS))

H2O

Comment (Liquid/ Veraenderung der kritischen Loesungstemperatur durch Zusaetze. Vapour Systems (MCS)) Timmermans; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 58; (1907); p. 196, View in Reaxys 53 of 53

Description (Liquid/ Boiling points of mixtures Vapour Systems (MCS)) Pressure (Liquid/Vapour 14 - 766 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

water

Konowalow; Annalen der Physik (Weinheim, Germany); <N.F.>14,45, View in Reaxys Magnetic Susceptibility (3) Magnetic SusTemperature ceptibility (Magnetic Sus[10-6cm3mol-1] ceptibility) [°C]

References

Bhatnagar; Luther; Journal of the Indian Chemical Society; vol. 6; (1929); p. 304; Chem. Zentralbl.; vol. 100; nb. II; (1929); p. 1270, View in Reaxys; Angus; Hill; Transactions of the Faraday Society; vol. 39; (1943); p. 192, View in Reaxys; Broersma; Journal of Chemical Physics; vol. 17; (1949); p. 874, View in Reaxys; French; Transactions of the Faraday Society; vol. 43; (1947); p. 357; Chem.Abstr.; (1948); p. 430, View in Reaxys; Farquharson; Sastri; Transactions of the Faraday Society; vol. 33; (1937); p. 1472, View in Reaxys; Bhatnagar; Mitra; Tuli; Phil.Mag.; vol. <7>18; (1934); p. 449, View in Reaxys; Bhatnagar; Mathur; Phil.Mag.; vol. <7>6; (1928); p. 917,221, View in Reaxys; Bhatnagar; Mitra; Journal of the Indian Chemical Society; vol. 13; (1936); p. 332; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 838, View in Reaxys; Mathur; Indian Journal of Physics (1926-1976); vol. 6; (1931); p. 207,215, View in Reaxys; Angus; Bulletin de la Societe Chimique de France; (1949); p. 483, View in Reaxys; Sriraman; Thiruvengadathan; Bulletin of the Chemical Society of Japan; vol. 34; (1961); p. 1560, View in Reaxys; Hoiland; Vikingsstad; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 72; (1976); p. 1441,1443, 1444, View in Reaxys; Gupta et al.; Journal of Chemical Physics; vol. 66; (1977); p. 4961, View in Reaxys; Ergin et al.; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 180; ; p. 303, View in Reaxys -54.1

-195

Hoarau; Annales de Chimie (Cachan, France); vol. <13>1; (1956); p. 544,554, View in Reaxys

-56

Prasad et al.; Proceedings - Indian Academy of Sciences, Section A; vol. 32; (1950); p. 313,314, View in Reaxys

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Mechanical & Physical Properties (MCS) (12) 1 of 12

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

H2O

Casanova, C.; Emmerich, Wilhelm; Grolier, J.-P. E.; Kehiaian, H. V.; Journal of Chemical Thermodynamics; vol. 13; nb. 3; (1981); p. 241 - 248, View in Reaxys; Granados, Karla; Gracia-Fadrique, Jesus; Amigo, Alfredo; Bravo, Ramon; Journal of Chemical and Engineering Data; vol. 51; nb. 4; (2006); p. 1356 - 1360, View in Reaxys 2 of 12

Description (Mechanical & Physical Properties (MCS))

Excess partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Comment (Mechanical & Physical Properties (MCS))

concentration dependence. Object(s) of Study: diagram

Partner (Mechanical & Physical Properties (MCS))

propyl cyanide

Letcher, Trevor M; Redhi, Gan G; Journal of Chemical Thermodynamics; vol. 33; nb. 11; (2001); p. 1499 - 1509, View in Reaxys 3 of 12

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

acetonitrile

Letcher; Redhi; Journal of Chemical and Engineering Data; vol. 45; nb. 1; (2000); p. 57 - 60, View in Reaxys 4 of 12

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Pressure (Mechanical & Physical Properties (MCS)) [Torr]

750.06 - 450036

Partner (Mechanical & Physical Properties (MCS))

di-isopropyl ether

Ulbig; Geyer; Gross; Schulz; Journal of Chemical and Engineering Data; vol. 43; nb. 2; (1998); p. 175 - 177, View in Reaxys 5 of 12

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

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Partner (Mechanical & Physical Properties (MCS))

toluene

Liron; Cohen; Journal of Pharmaceutical Sciences; vol. 72; nb. 5; (1983); p. 499 - 504, View in Reaxys 6 of 12

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

tetrachloromethane

Liron; Cohen; Journal of Pharmaceutical Sciences; vol. 72; nb. 5; (1983); p. 499 - 504, View in Reaxys 7 of 12

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

acetone

Stairs, Robert A.; Canadian Journal of Chemistry; vol. 58; nb. 3; (1980); p. 296 - 301, View in Reaxys 8 of 12

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

King; Journal of Physical Chemistry; vol. 73; (1969); p. 1220,1222,1223, View in Reaxys; Hoeiland; Acta Chemica Scandinavica (1947-1973); vol. 27; (1973); p. 2687,2689,2691, View in Reaxys 9 of 12

Description (Mechanical & Physical Properties (MCS))

Adiabatic compressibility

Tsvetkov; Rabinovich; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 1692; ; p. 2962, View in Reaxys; Rao; Rao; Indian Journal of Pure and Applied Physics; vol. 3; (1965); p. 207, View in Reaxys 10 of 12

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Comment (Mechanical & Physical Properties (MCS))

Aenderung des partiellen Molvolumens bei der Dissoziation in Wasser.

Hamann; Lim; Australian Journal of Chemistry; vol. 7; (1954); p. 329,330, View in Reaxys 11 of 12

Description (Mechanical & Physical Properties (MCS))

Adiabatic compressibility

Solvent (Mechanical & Physical Properties (MCS))

H2O

Temperature (Mechanical & Physical Properties (MCS)) [°C]

24.5 - 29

Venkateswaran; Journal of Physical Chemistry; vol. 31; (1927); p. 1523, View in Reaxys

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12 of 12

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Partner (Mechanical & Physical Properties (MCS))

water

Pound; Russell; Journal of the Chemical Society; vol. 125; (1924); p. 780, View in Reaxys Mechanical Properties (5) Description (MeComment (Mechanical Properchanical Properties) ties)

References

Molar volume

Raman; Naidu; Proceedings - Indian Academy of Sciences, Section A; vol. 75; (1972); p. 68, View in Reaxys; Kauzmann et al.; Journal of the American Chemical Society; vol. 84; (1962); p. 1777,1780, View in Reaxys; Palma; Morel; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 73; (1976); p. 645,648, View in Reaxys; Hargreaves; Kresheck; Journal of Physical Chemistry; vol. 73; (1969); p. 3249, View in Reaxys; Kojima et al.; Journal of Inorganic and Nuclear Chemistry; vol. 32; (1970); p. 987,989, View in Reaxys; Hoiland; Acta Chemica Scandinavica, Series A: Physical and Inorganic Chemistry; vol. 28; (1974); p. 699, View in Reaxys; Kovrigina; Bogdanov; Russian Journal of Physical Chemistry; vol. 44; (1970); p. 881; ; p. 1571, View in Reaxys; Hoeiland; Acta Chemica Scandinavica (1947-1973); vol. 27; (1973); p. 2687,2689,2691, View in Reaxys; Pointud; Juillard; Journal of the Chemical Society Faraday Transactions I; vol. 77; nb. 1; (1981); p. 1 - 8, View in Reaxys

Viscosity

Fialkov; Russian Journal of Physical Chemistry; vol. 37; (1963); p. 1051; ; p. 1938, View in Reaxys; Kotisek; Marek; Chemicky Prumysl; vol. 5; (1955); p. 330,331, 332; Chem.Abstr.; nb. 6239; (1960), View in Reaxys; Raman; Naidu; Proceedings - Indian Academy of Sciences, Section A; vol. 75; (1972); p. 68, View in Reaxys; Ssumarokowa; Nurmakowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 29,29; Chem.Abstr.; nb. 19134; (1960), View in Reaxys; Palma; Morel; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 73; (1976); p. 645,648, View in Reaxys; Fieggen; Recueil des Travaux Chimiques des Pays-Bas; vol. 89; (1970); p. 625,633, View in Reaxys; Kynaston; Martin; Journal of Applied Chemistry and Biotechnology; vol. 27; (1977); p. 296,299,301, View in Reaxys; Timrot et al.; High Temperature; vol. 14; (1976); p. 1068; ; p. 1192, View in Reaxys

Compressibility

Luzkii; Solon'ko; Russian Journal of Physical Chemistry; vol. 38; (1964); p. 778; Zhurnal Fizicheskoi Khimii; vol. 38; (1964); p. 1421, View in Reaxys

PVT Relationship

bei Temperaturen Lundin et al.; Journal of the American Chemical Society; vol. 74; (1952); p. 743, von 141.4grad bis View in Reaxys 195.5grad und Drucken von 242.7 Torr bis 717.5 Torr.

Volume change on melting

Sackmann; Sauerwald; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 195; (1950); p. 295,303, View in Reaxys

Molecular Deformation (2) Description (MoComment (Molec- References lecular Deforma- ular Deformation) tion) Fundamental vibrations

von binaer asso- Corish; Chapman; Journal of the Chemical Society; (1957); p. 1746, View in Reaxys; zierter ButterHayashi et al.; Bulletin of the Institute for Chemical Research, Kyoto University; vol. 46; saeure im krystal- (1968); p. 213,216, View in Reaxys linen und im fluessigen Zustand.

Fundamental vibrations

Hayashi et al.; Bulletin of the Institute for Chemical Research, Kyoto University; vol. 46; (1968); p. 213,216, View in Reaxys

Optical Rotatory Power (1) 1 of 1

Patent; Warner-Lambert Company; US5397788; (1995); (A1) English, View in Reaxys

Optics (15) Description (Optics)

Comment (Optics)

References

166/428

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Rayleigh scattering

Lupina; Lanshina; Moscow University Chemistry Bulletin (English Translation); vol. 25; nb. 3; (1970); p. 61; ; p. 359, View in Reaxys

Magnetorotation

Gallais,F. et al.; Bulletin de la Societe Chimique de France; (1960); p. 2157 - 2169, View in Reaxys; Grillet; Bulletin de la Societe Scientifique de Bretagne; vol. 17; (1940); p. 125; Chem.Abstr.; (1946); p. 3321, View in Reaxys; Broersma et al.; Physica; vol. 10; (1943); p. 111, View in Reaxys; Lewis; Evans; Phil.Mag.; vol. <7>13; (1932); p. 272, View in Reaxys

Degree of depola- Intensitaet und Bai; Proceedings - Indian Academy of Sciences, Section A; vol. 15; (1942); p. 359; rization of RayDepolarisationsChem.Abstr.; (1943); p. 35, View in Reaxys leigh scattering grad des an fluessiger Buttersaeure gestreuten Lichts bei Temperaturen bis 140grad. Degree of depola- Intensitaet und rization of RayDepolarisationsleigh scattering grad des an fluessiger Buttersaeure gestreuten Lichts.

Canals; Peyrot; Noel; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 201; (1935); p. 209, View in Reaxys; Canals; Peyrot; Journal de Pharmacie et de Chimie; vol. <8>23; (1936); p. 296, View in Reaxys; Krishnan; Proceedings - Indian Academy of Sciences, Section A; vol. 3; (1936); p. 130; Chem. Zentralbl.; vol. 107; nb. I; (1936); p. 4890, View in Reaxys; Peyrot; Annales de Physique (Paris, France); vol. <11> 9; (1938); p. 335,360, 376, View in Reaxys

Magnetic birefringence (CottonMouton effect)

Chinchalkar; Indian Journal of Physics (1926-1976); vol. 6; (1931); p. 172, View in Reaxys; Piekara; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 199; (1934); p. 527, View in Reaxys; Ramanadham; Indian J.Phys.; vol. 4; p. 27; Chem. Zentralbl.; vol. 100; nb. II; (1929); p. 2315, View in Reaxys

Reflection

Elliptische Polari- Bouhet; Annales de Physique (Paris, France); vol. <10> 15; (1931); p. 5,35, sation von linear View in Reaxys polarisiertem Licht bei der Reflexion an den Oberflaechen von Buttersaeure und von wss.Buttersaeure-Loesungen.

Diffraction

von Roentgenstrahlen in fluessiger Buttersaeure.

Diffraction

von RoentgenVaidyanathan; Indian J.Phys.; vol. 3; p. 394; Chem. Zentralbl.; vol. 100; nb. I; (1929); p. strahlen durch 2950, View in Reaxys fluessige Buttersaeure bei 30grad und 120grad.

Diffraction

von Roentgenstrahlen durch waessr.Buttersaeure-Loesungen.

Ishino; Tanaka; Tsuji; Memoirs of the College of Science, Kyoto Imperial University; 13<A><1930>22; Chem. Zentralbl.; vol. 101; nb. I; (1930); p. 3001, View in Reaxys; Trillat; Zeitschrift fuer Physik; vol. 64; (1930); p. 199; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 190; (1930); p. 859, View in Reaxys

Krishnamurti; Indian J.Phys.; vol. 3; p. 353; Chem. Zentralbl.; vol. 100; nb. I; (1929); p. 2951, View in Reaxys

Degree of depola- Intensitaet und rization of RayPolarisationszuleigh scattering stand des Streulichts bei der Streuung von Licht in fluessiger Buttersaeure.

Krishnan; Phil.Mag.; vol. <6>50; p. 703; Chem. Zentralbl.; vol. 97; nb. I; (1926); p. 838, View in Reaxys; Venkateswaran; Indian J.Phys.; vol. 1; p. 395, View in Reaxys; R.Rao,S.; Indian J.Phys.; vol. 3; p. 12; Chem. Zentralbl.; vol. 100; nb. I; (1929); p. 20, View in Reaxys

Reflection

Lichtreflexion durch Oberflaechen von Buttersaeure.

Bhatnagar; Shrivastava; Mitra; Journal of the Indian Chemical Society; vol. 5; (1928); p. 336; Chem. Zentralbl.; vol. 99; nb. II; (1928); p. 1745, View in Reaxys

Diffraction

von Roentgenstrahlen durch fluessige Butter-

Stewart; Mannheimer; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 171; (1928); p. 68, View in Reaxys; Morrow; Physical Review; vol. <2>31; (1928); p. 11; Chem. Zentralbl.; vol. 99; nb. I; (1928); p. 2693, View in Reaxys; Katz; Angewandte

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saeure bei gewoehnlicher Temperatur.

Chemie; vol. 41; (1928); p. 337; Zeitschrift fuer Physik; vol. 45; p. 101; Chem. Zentralbl.; vol. 99; nb. I; (1928); p. 154, View in Reaxys; Sogani; Indian J.Phys.; vol. 2; p. 102; Chem. Zentralbl.; vol. 99; nb. I; (1928); p. 470, View in Reaxys

Degree of depola- Intensitaet und rization of RayPolarisationszuleigh scattering stand des Streulichts bei der Streuung von Licht in Buttersaeure-Dampf.

R.Rao,I.; Indian J.Phys.; vol. 2; p. 83; Chem. Zentralbl.; vol. 99; nb. I; (1928); p. 1838, View in Reaxys

Degree of depola- Intensitaet und rization of RayPolarisationszuleigh scattering stand des Streulichts bei der Streuung von Licht in waessr.Buttersaeure-Loesung.

Venkateswaran; Indian J.Phys.; vol. 1; p. 395; Chem. Zentralbl.; vol. 98; nb. II; (1927); p. 2534, View in Reaxys

Degree of depola- Intensitaet und rization of RayPolarisationszuleigh scattering stand des Streulichts bei der Streuung von Licht an Buttersaeure-Oberflaechen.

Raman; Ramdas; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 109; (1925); p. 274; Chem. Zentralbl.; vol. 97; nb. I; (1926); p. 838, View in Reaxys; Ramdas; Indian J.Phys.; vol. 1; p. 221; Chem. Zentralbl.; vol. 98; nb. II; (1927); p. 2535, View in Reaxys

Other Thermochemical Data (9) Description (Oth- Comment (Other er Thermochemi- Thermochemical cal Data) Data)

References

Enthalpy of selfassociation

Miyamoto, Shinji; Nakamura, Shinichi; Iwai, Yoshio; Arai, Yasuhiko; Journal of Chemical and Engineering Data; vol. 44; nb. 1; (1999); p. 48 - 51, View in Reaxys

Entropy

Morel et al.; Journal of Solution Chemistry; vol. 3; (1974); p. 403, View in Reaxys; Martin, J. F.; Andon, R. J. L.; Journal of Chemical Thermodynamics; vol. 14; nb. 7; (1982); p. 679 - 688, View in Reaxys

Enthalpy

Stern et al.; Journal of Chemical and Engineering Data; vol. 24; (1979); p. 314, View in Reaxys; Kuo; Chen; Journal of the Chinese Chemical Society (Taipei, Taiwan); vol. 23; (1976); p. 61, View in Reaxys

Thermodynamic properties

Benoit; Harrison; Journal of the American Chemical Society; vol. 99; (1977); p. 3980,3981, View in Reaxys; Christensen et al.; Journal of the American Chemical Society; vol. 89; (1967); p. 213, View in Reaxys; Konicek; Wadsoe; Acta Chemica Scandinavica (1947-1973); vol. 25; (1971); p. 1541,1543,1545, View in Reaxys; Calis-van Ginkel et al.; Journal of Chemical Thermodynamics; vol. 10; (1978); p. 1083,1087, 1088, View in Reaxys; Kuo; Chen; Journal of the Chinese Chemical Society (Taipei, Taiwan); vol. 23; (1976); p. 61, View in Reaxys; Loutfy; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 41; (1973); p. 27,28, View in Reaxys; Dash; Thermochimica Acta; vol. 32; (1979); p. 33,34, View in Reaxys; Kolesnikov et al.; Russian Journal of Physical Chemistry; vol. 52; (1978); p. 1122; ; p. 1941, View in Reaxys; Breslauer et al.; Journal of Physical Chemistry; vol. 78; (1974); p. 2363, View in Reaxys; Sano et al.; Bulletin of the Chemical Society of Japan; vol. 45; (1972); p. 2669, View in Reaxys

Cryoscopic constant

Kryoskopisches Verhalten in Benzol:.

Giacalone; Gazzetta Chimica Italiana; vol. 72; (1942); p. 431, View in Reaxys; Meisenheimer; Dorner; Justus Liebigs Annalen der Chemie; vol. 523; (1936); p. 301, View in Reaxys

Cryoscopic constant

Kryoskopisches Verhalten in Wasser:.

Giacalone; Gazzetta Chimica Italiana; vol. 70; (1940); p. 55, View in Reaxys

Cryoscopic constant

Kryoskopisches Verhalten in Cyclohexan:.

Broughton; Transactions of the Faraday Society; vol. 30; (1934); p. 368, View in Reaxys

Cryoscopic constant

Kryoskopisches Verhalten in Ben-

Francois; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 193; (1931); p. 1010, View in Reaxys; Boutaric; Roy; Journal de Pharmacie et de Chimie; vol. <8> 15; (1932); p. 161; Chem. Zentralbl.; vol. 103; nb. II; (1932); p. 1041, View in Reaxys

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zol und Nitrobenzol:. Heat of combustion at constant volume

521.6 kcal/Mol.

Landolt-Boernst. E II,1641, View in Reaxys; Verkade; Coops; Recueil des Travaux Chimiques des Pays-Bas; vol. 47; (1928); p. 608; Recueil des Travaux Chimiques des PaysBas; vol. 52; (1933); p. 254, View in Reaxys

Partition octan-1-ol/water (MCS) (2) 1 of 2

log POW

0.777

Patent; SUNTORY FLOWERS LIMITED; US2009/119801; (2009); (A1) English, View in Reaxys 2 of 2

log POW

0.79

Perminova, Irina V.; Frimmel, Fritz H.; Kovalevskii, Dmitrii V.; Abbt-Braun, Gudrun; Kudryavtsev, Alexey V.; Hesse, Sebastian; Water Research; vol. 32; nb. 3; (1998); p. 872 - 881, View in Reaxys Solubility (MCS) (4) 1 of 4

Comment (Solubility (MCS))

soluble in CH2Cl2

Nalder, Tim D.; Ashton, Trent D.; Pfeffer, Frederick M.; Marshall, Susan N.; Barrow, Colin J.; Biochimie; vol. 128-129; (2016); p. 127 - 132, View in Reaxys 2 of 4

Comment (Solubility (MCS))

Loeslichkeits-Parameter in versch. Loesungsmitteln (Tab. 3)

Korenman et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 47; (1974); p. 2075,2130, View in Reaxys 3 of 4

Comment (Solubility (MCS))

Loeslichkeit (T) v. Cyclopropan in n-Buttersaeure

Barton; Hsu; Journal of Chemical and Engineering Data; vol. 16; (1971); p. 93,94, View in Reaxys 4 of 4

Comment (Solubility (MCS))

critical solution temperature with D2O and H2O given;

Patterson, W. H.; Journal of the Chemical Society; (1938); p. 1559 - 1561, View in Reaxys; Poppe, G.; Bulletin des Societes Chimiques Belges; vol. 44; (1935); p. 640 - 657, View in Reaxys; Timmermans, J.; Poppe, G.; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 201; (1935); p. 524 - 527, View in Reaxys; vol. O: MVol.6; 70, page 1985 - 1988 ; (from Gmelin), View in Reaxys Solution Behaviour (MCS) (18) 1 of 18

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

Comment (Solution Behaviour (MCS))

temperature dependence

Partner (Solution Behaviour (MCS))

water; pyridine

Cherkasov; Smotrov; Il'in; Russian Journal of Applied Chemistry; vol. 81; nb. 2; (2008); p. 218 - 222, View in Reaxys 2 of 18

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

Partner (Solution Behaviour (MCS))

water; pyridine

Cherkasov; Smotrov; Il'in; Russian Journal of Applied Chemistry; vol. 81; nb. 2; (2008); p. 218 - 222, View in Reaxys 3 of 18

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

Partner (Solution Behaviour (MCS))

water; pyridine

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Cherkasov; Smotrov; Il'in; Russian Journal of Applied Chemistry; vol. 81; nb. 2; (2008); p. 218 - 222, View in Reaxys 4 of 18

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

Partner (Solution Behaviour (MCS))

water; pyridine

Cherkasov; Smotrov; Il'in; Russian Journal of Applied Chemistry; vol. 81; nb. 2; (2008); p. 218 - 222, View in Reaxys 5 of 18

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

Partner (Solution Behaviour (MCS))

water; pyridine

Cherkasov; Smotrov; Il'in; Russian Journal of Applied Chemistry; vol. 81; nb. 2; (2008); p. 218 - 222, View in Reaxys 6 of 18

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

Partner (Solution Behaviour (MCS))

water; pyridine

Cherkasov; Smotrov; Il'in; Russian Journal of Applied Chemistry; vol. 81; nb. 2; (2008); p. 218 - 222, View in Reaxys 7 of 18

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

51.5

Partner (Solution Behaviour (MCS))

water; pyridine

Cherkasov; Smotrov; Il'in; Russian Journal of Applied Chemistry; vol. 81; nb. 2; (2008); p. 218 - 222, View in Reaxys 8 of 18

Description (Solution Behaviour (MCS))

Mutual solubility

Solvent (Solution Behaviour (MCS))

2,2,4-trimethyl-pentane

Temperature (Solution Behaviour (MCS)) [°C]

Partner (Solution Behaviour (MCS))

griseofulvin

Mehdizadeh; Grant; Journal of Pharmaceutical Sciences; vol. 73; nb. 9; (1984); p. 1195 - 1203, View in Reaxys 9 of 18

Description (Solution Behaviour (MCS))

Dissolving capacity

Markowitz et al.; Journal of Chemical and Engineering Data; vol. 6; (1961); p. 325, View in Reaxys; Mayer; Hoffmann; Journal fuer Praktische Chemie (Leipzig); vol. 11; (1960); p. 327,329, View in Reaxys; Nikolaew et al.; Izvestiya Sibirskogo Otdeleniya Akademii Nauk SSSR; vol. 4; (1971); p. 78, View in Reaxys; Zheleznyak; Krestov; Journal of Structural Chemistry; vol. 19; (1978); p. 704,707; ; p. 818, View in Reaxys; Balashov; Serafimov; J. Appl. Chem. USSR (Engl. Transl.); vol. 39; (1966); p. 901,845,846-848, View in Reaxys; Muchnik et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 48; (1975); p. 1322,1373, View in Reaxys 10 of 18

Description (Solution Behaviour (MCS))

Miscibility

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Dubovskaya; Karapet'yants; Russian Journal of Physical Chemistry; vol. 44; (1970); p. 1300, View in Reaxys 11 of 18

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Behaviour (MCS)) [°C]

25 - 50

Partner (Solution Behaviour (MCS))

radon

Nussbaum; Hursh; Journal of Physical Chemistry; vol. 62; (1958); p. 81, View in Reaxys 12 of 18

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Behaviour (MCS)) [°C]

9.6 - 43.8

Partner (Solution Behaviour (MCS))

hydrogenchloride

Gerrard; Macklen; Journal of Applied Chemistry; vol. 6; (1956); p. 241,243, View in Reaxys 13 of 18

Description (Solution Behaviour (MCS))

Miscibility

Solvent (Solution Behaviour (MCS))

H2O

Comment (Solution Behaviour (MCS))

Mischbarkeitstemperatur.

Patterson; Journal of the Chemical Society; (1938); p. 1560, View in Reaxys 14 of 18

Description (Solution Behaviour (MCS))

Miscibility

Solvent (Solution Behaviour (MCS))

D2O

Comment (Solution Behaviour (MCS))

Mischbarkeitstemperatur.

Patterson; Journal of the Chemical Society; (1938); p. 1560, View in Reaxys 15 of 18

Description (Solution Behaviour (MCS))

Miscibility

Solvent (Solution Behaviour (MCS))

H2O; D2O

Comment (Solution Behaviour (MCS))

Mischbarkeitstemperatur.

Patterson; Journal of the Chemical Society; (1938); p. 1560, View in Reaxys 16 of 18

Description (Solution Behaviour (MCS))

Miscibility

Comment (Solution Behaviour (MCS))

bei Drucken bis 149 atm.

Partner (Solution Behaviour (MCS))

D2O

Poppe; Bulletin des Societes Chimiques Belges; vol. 44; (1935); p. 644, View in Reaxys 17 of 18

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

methyl orange

Dehn; Journal of the American Chemical Society; vol. 39; (1917); p. 1379, View in Reaxys 18 of 18

Description (Solution Behaviour (MCS))

Miscibility

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Temperature (Solution Behaviour (MCS)) [°C]

-3.8

Comment (Solution Behaviour (MCS))

unterhalb dies.Temp.sind Gemische mit 25-60prozent Saeure nicht homogen.

Partner (Solution Behaviour (MCS))

water

References

Velocity of sound

Tsvetkov; Rabinovich; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 1692; ; p. 2962, View in Reaxys; Lutskii; Solon'ko; Russian Journal of Physical Chemistry; vol. 39; (1965); p. 414; ; p. 783, View in Reaxys; Hustad et al.; Chemistry and Physics of Lipids; vol. 7; (1971); p. 61,65, View in Reaxys; Rao; Rao; Current Science; vol. 40; (1971); p. 372, View in Reaxys; Rao; Reddy; Current Science; vol. 48; (1979); p. 247, View in Reaxys

Ultrasonic properties

Rao; Rao; Journal of Scientific and Industrial Research, Section B: Physical Sciences; vol. 21; (1962); p. 331,332, View in Reaxys; Zheleznyak; Krestov; Journal of Structural Chemistry; vol. 19; (1978); p. 704,707; ; p. 818, View in Reaxys; Plass; Berichte der Bunsen-Gesellschaft; vol. 74; (1970); p. 343,344-346, View in Reaxys; RAO CR; KRISHNA RAO PSR; SUBRAHMANYAM P; Indian Journal of Pure and Applied Physics; vol. 9; nb. 6; (1971); p. 400 - 401, View in Reaxys; Sano et al.; Bulletin of the Chemical Society of Japan; vol. 45; (1972); p. 2669, View in Reaxys

Sound absorption

Michels; Zana; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 66; (1969); p. 240, View in Reaxys; Stumpf; Crum; Journal of the Acoustical Society of America; vol. 39; (1966); p. 170, View in Reaxys

Velocity of sound

bei 30grad.

Sound absorption

bei 0grad,25grad White; Benson; Canadian Journal of Chemistry; vol. 36; (1958); p. 1135, View in Reaxys und 38.4grad und Frequenzen von 1 MHz bis 9 MHz.

Sound absorption

bei 30grad und Frequenzen von 1.4 MHz bis 15.8 MHz.

Parthasarathy et al.; Nuovo Cimento; vol. <10>10; (1958); p. 111,113, View in Reaxys

Velocity of sound

in Buttersaeure bei 20grad: 1234 m/sec.

Zwetkow; Marinin; Doklady Akademii Nauk SSSR; vol. 68; (1949); p. 52; Chem.Abstr.; (1949); p. 8786, View in Reaxys

Velocity of sound

in Buttersaeure bei 20grad: 1203 m/sec.

Schaaffs; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 194; (1944); p. 28,33, 39, 48; Annalen der Physik (Weinheim, Germany); vol. <5> 40; (1941); p. 393,402, View in Reaxys

Velocity of sound

Temperaturkoeffizient.

Schaaffs; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 194; (1944); p. 28,33, 39, 48; Annalen der Physik (Weinheim, Germany); vol. <5> 40; (1941); p. 393,402, View in Reaxys

Space Group (2) Space Group 10; 12

Parthasarathy et al.; Nuovo Cimento; vol. <10>10; (1958); p. 111,113, View in Reaxys

References Strieter; U.S.Atomic Energy Comm.UCRL-8906; <1959>30, View in Reaxys; Strieter; Templeton; Acta Crystallographica; vol. 15; (1962); p. 1240,1243, View in Reaxys Strieter; Templeton; Acta Crystallographica; vol. 15; (1962); p. 1240,1243, View in Reaxys

Static Dielectric Constant (2) Static Dielectric Temperature Constant (Static Dielectric Constant) [°C]

References

3.055

Phadke; Journal of the Indian Institute of Science, Section A; vol. 34; (1952); p. 293,294, View in Reaxys

2.9

Tomecko; Hatcher; Trans.roy.Soc.Canada; vol. <3>45; (1951); p. 39,42, View in Reaxys

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Surface Tension (20) Surface Tension Temperature [g·s-2] (Surface Tension) [°C]

References

23.41

44.99

Ahluwalia; Gupta, Ritu; Vashisht; Wanchoo; Journal of Solution Chemistry; vol. 42; nb. 5; (2013); p. 945 - 966, View in Reaxys

24.33

34.99

Ahluwalia; Gupta, Ritu; Vashisht; Wanchoo; Journal of Solution Chemistry; vol. 42; nb. 5; (2013); p. 945 - 966, View in Reaxys

25.31

24.99

Ahluwalia; Gupta, Ritu; Vashisht; Wanchoo; Journal of Solution Chemistry; vol. 42; nb. 5; (2013); p. 945 - 966, View in Reaxys

26.71

19.99

Suarez, Felipe; Romero, Carmen M.; Journal of Chemical and Engineering Data; vol. 56; nb. 5; (2011); p. 1778 - 1786, View in Reaxys

26.21

24.99

Suarez, Felipe; Romero, Carmen M.; Journal of Chemical and Engineering Data; vol. 56; nb. 5; (2011); p. 1778 - 1786, View in Reaxys

25.61

29.99

Suarez, Felipe; Romero, Carmen M.; Journal of Chemical and Engineering Data; vol. 56; nb. 5; (2011); p. 1778 - 1786, View in Reaxys

25.07

34.99

Suarez, Felipe; Romero, Carmen M.; Journal of Chemical and Engineering Data; vol. 56; nb. 5; (2011); p. 1778 - 1786, View in Reaxys

26.19

Granados, Karla; Gracia-Fadrique, Jesus; Amigo, Alfredo; Bravo, Ramon; Journal of Chemical and Engineering Data; vol. 51; nb. 4; (2006); p. 1356 - 1360, View in Reaxys Wright; Akhtar; Journal of the Chemical Society [Section] B: Physical Organic; (1970); p. 151,152-153, View in Reaxys

3.4 - 27

20 - 300

Woljak; Andreewa; Trudy Moskovsk.aviac.Inst.; nb. 51; (1955); p. 35; Chem.Abstr.; (1958); p. 8662, View in Reaxys

20.32 - 26.26

22.5 - 87.3

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

26.57

13.5 - 16

Kosakewitsch, P. P.; Kosakewitsch, N. S.; Z. phys. Ch.; vol. 166; (1933); p. 113 - 135, View in Reaxys; vol. Ca: MVol.B2; 112, page 531 - 533 ; (from Gmelin), View in Reaxys

25.57

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys

26.74

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys

27.32

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys

16.4 - 29.2

0.1 - 131.3

Hunten; Maass; Journal of the American Chemical Society; vol. 51; (1929); p. 159, View in Reaxys

26.88

Tominaga; Biochemische Zeitschrift; vol. 140; (1923); p. 245, View in Reaxys

23.37

46.5

Morgan; Stone; Journal of the American Chemical Society; vol. 35; (1913); p. 1517, View in Reaxys

26.44

Morgan; Stone; Journal of the American Chemical Society; vol. 35; (1913); p. 1517, View in Reaxys

16.44 - 26.74

15 - 132.3

Ramsay; Shields; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 12; (1893); p. 455, View in Reaxys

Transport Data (1) Description References (Transport Data) Thermal conductivity

Kynaston; Martin; Journal of Applied Chemistry and Biotechnology; vol. 27; (1977); p. 296,299,301, View in Reaxys; Usmanov; Salikhov; Russian Journal of Physical Chemistry; vol. 49; (1975); p. 1124; ; p. 1911, View in Reaxys

Transport Phenomena (MCS) (43) 1 of 43

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C]

173/428

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Partner (Transport Phenomena (MCS))

1,4-dioxane

Roy, Mahendra Nath; Sinha, Biswajit; Dakua, Vikas Kumar; Journal of Chemical and Engineering Data; vol. 51; nb. 2; (2006); p. 590 - 594, View in Reaxys 2 of 43

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

1,3-DIOXOLANE

Roy, Mahendra Nath; Sinha, Biswajit; Dakua, Vikas Kumar; Journal of Chemical and Engineering Data; vol. 51; nb. 2; (2006); p. 590 - 594, View in Reaxys 3 of 43

Description (Transport Phenomena (MCS))

Thermal diffusion (Soret coefficient)

Temperature (Transport 25 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

concentration dependence

Partner (Transport Phenomena (MCS))

H2O

Domonkos; Liszi; Zeitschrift fur Physikalische Chemie; vol. 214; nb. 1; (2000); p. 55 - 64, View in Reaxys 4 of 43

Description (Transport Phenomena (MCS))

Diffusion coefficient

Temperature (Transport 25 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

H2O

Domonkos; Liszi; Zeitschrift fur Physikalische Chemie; vol. 214; nb. 1; (2000); p. 55 - 64, View in Reaxys 5 of 43

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

H2O; aq. NaOH

Temperature (Transport 24.9 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

decane; membrane

Hanna, Gregory J.; Noble, Richard D.; Michael, Frederick C.; Journal of Physical Chemistry; vol. 91; nb. 2; (1987); p. 362 - 365, View in Reaxys 6 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 15 - 35 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

H2O

Miyajima; Sawada; Nakagaki; Bulletin of the Chemical Society of Japan; vol. 56; nb. 3; (1983); p. 827 - 830, View in Reaxys 7 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

acetone

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Stairs, Robert A.; Canadian Journal of Chemistry; vol. 58; nb. 3; (1980); p. 296 - 301, View in Reaxys 8 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 25.1 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

triethylamine

Huyskens, P.; Felix, N.; Janssens, A.; Broeck, F. Van den; Kapuku, F.; Journal of Physical Chemistry; vol. 84; nb. 11; (1980); p. 1387 - 1393, View in Reaxys 9 of 43

Description (Transport Phenomena (MCS))

Viscosity

Singh; Singh; Journal of the Indian Chemical Society; vol. 55; (1978); p. 738, View in Reaxys; Raman; Naidu; Proceedings - Indian Academy of Sciences, Section A; vol. 75; (1972); p. 68, View in Reaxys; Motscharnjuk; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 1086,1103; Chem.Abstr.; nb. 23624; (1960), View in Reaxys; Kusnezow; Smirnow; J. Appl. Chem. USSR (Engl. Transl.); vol. 34; (1961); p. 1954,1859; Chem.Abstr.; nb. 3318; (1962), View in Reaxys; Ssumarokowa; Nurmakowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 29,29; Chem.Abstr.; nb. 19134; (1960), View in Reaxys 10 of 43

Description (Transport Phenomena (MCS))

Diffusion

Lugg; Analytical Chemistry; vol. 40; (1968); p. 1072,1074, View in Reaxys; Amourdam; Laddha; Journal of Chemical and Engineering Data; vol. 12; (1967); p. 389, View in Reaxys; BERG; GUESS; AUTIAN; Journal of pharmaceutical sciences; vol. 54; (1965); p. 79 - 84, View in Reaxys; Bidstrup; Geankoplis; Journal of Chemical and Engineering Data; vol. 8; (1963); p. 170, View in Reaxys; Dunn; Stokes; Australian Journal of Chemistry; vol. 18; (1965); p. 285,286-296, View in Reaxys; Lileewa; Smirnow; J. Appl. Chem. USSR (Engl. Transl.); vol. 34; (1961); p. 1361,1295; Chem.Abstr.; nb. 21695; (1961), View in Reaxys; Hertz; Tutsch; Berichte der Bunsen-Gesellschaft; vol. 80; (1976); p. 1268,1272, View in Reaxys 11 of 43

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport 20 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

Diffusionskoeffizient.

Partner (Transport Phenomena (MCS))

water

Rossi et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 55; (1958); p. 91,93, View in Reaxys 12 of 43

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport 21.5 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

Diffusionskoeffizient.

Partner (Transport Phenomena (MCS))

tetrachloromethane

Marinin; Zhurnal Fizicheskoi Khimii; vol. 27; (1953); p. 1823,1825; Chem.Abstr.; (1954); p. 9775, View in Reaxys 13 of 43

Description (Transport Phenomena (MCS))

Diffusion

Comment (Transport Phenomena (MCS))

durch die Phasengrenze zwischen Wasser und Toluol.

Ward; Brooks; Transactions of the Faraday Society; vol. 48; (1952); p. 1124, View in Reaxys 14 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C]

175/428

2017-08-01 04:43:04

Comment (Transport Phenomena (MCS))

Nachweis einer Verbindung C10H14N2+3C4H8O2.

Partner (Transport Phenomena (MCS))

3-(1-methyl-pyrrolidin-2-yl)-pyridine

Babak; Zhurnal Obshchei Khimii; vol. 19; (1949); p. 1604,1606; Chem.Abstr.; (1940); p. 919, View in Reaxys 15 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 50 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

Nachweis einer Verbindung C10H14N2+3C4H8O2.

Partner (Transport Phenomena (MCS))

3-(1-methyl-pyrrolidin-2-yl)-pyridine

Babak; Zhurnal Obshchei Khimii; vol. 19; (1949); p. 1604,1606; Chem.Abstr.; (1940); p. 919, View in Reaxys 16 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 75 Phenomena (MCS)) [°C] Comment (Transport Phenomena (MCS))

Nachweis einer Verbindung C10H14N2+3C4H8O2.

Partner (Transport Phenomena (MCS))

3-(1-methyl-pyrrolidin-2-yl)-pyridine

Babak; Zhurnal Obshchei Khimii; vol. 19; (1949); p. 1604,1606; Chem.Abstr.; (1940); p. 919, View in Reaxys 17 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

tetrachloromethane

Jones et al.; Journal of Physical Chemistry; vol. 52; (1948); p. 755, View in Reaxys 18 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

benzene

Le Fevre; Vine; Journal of the Chemical Society; (1938); p. 1799, View in Reaxys; Jones et al.; Journal of Physical Chemistry; vol. 52; (1948); p. 755, View in Reaxys 19 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

nitrobenzene

Aleixandre; Anales de la Real Sociedad Espanola de Fisica y Quimica; vol. 40; (1944); p. 487; Chem.Abstr.; (1949); p. 6066, View in Reaxys 20 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

water

176/428

2017-08-01 04:43:04

Irany; Journal of the American Chemical Society; vol. 65; (1943); p. 1396, View in Reaxys 21 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

acetone

Udowenko; Zhurnal Obshchei Khimii; vol. 9; (1939); p. 1162; Chem. Zentralbl.; vol. 111; nb. II; (1940); p. 1562, View in Reaxys 22 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 35 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

acetone

Udowenko; Zhurnal Obshchei Khimii; vol. 9; (1939); p. 1162; Chem. Zentralbl.; vol. 111; nb. II; (1940); p. 1562, View in Reaxys 23 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 45 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

acetone

Udowenko; Zhurnal Obshchei Khimii; vol. 9; (1939); p. 1162; Chem. Zentralbl.; vol. 111; nb. II; (1940); p. 1562, View in Reaxys 24 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

benzene; acetone

Udowenko; Witjajewa; Zhurnal Obshchei Khimii; vol. 9; (1939); p. 1731; Chem. Zentralbl.; vol. 112; nb. I; (1941); p. 2096, View in Reaxys 25 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

benzene; 2-Pentanone

Udowenko; Airapetowa; Zhurnal Obshchei Khimii; vol. 9; (1939); p. 1796,1798, 1799; Chem. Zentralbl.; vol. 112; nb. I; (1941); p. 2095, View in Reaxys 26 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

pyrrole

Dezelic; Belia; Glasnik chem.Drustva Jugosl.; vol. 9; (1938); p. 166,174; Chem.Abstr.; (1940); p. 7289, View in Reaxys 27 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 Phenomena (MCS)) [°C]

177/428

2017-08-01 04:43:04

Partner (Transport Phenomena (MCS))

2,4-dimethyl-3-ethyl-pyrrole

Dezelic; Belia; Glasnik chem.Drustva Jugosl.; vol. 9; (1938); p. 166,174; Chem.Abstr.; (1940); p. 7289, View in Reaxys 28 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport -3 - 35 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

water

Bury; Grindley; Journal of the Chemical Society; (1936); p. 1003, View in Reaxys 29 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

o-toluidine

Angelescu; Eustatiu; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 177; (1936); p. 265, View in Reaxys 30 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 25 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

1-amino-3-methylbenzene

Angelescu; Eustatiu; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 177; (1936); p. 265, View in Reaxys 31 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 10 - 70 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

benzene

Smyth; Rogers; Journal of the American Chemical Society; vol. 52; (1930); p. 1826, View in Reaxys 32 of 43

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

H2O

Comment (Transport Phenomena (MCS))

durch Mantelgewebe von Nudibranchia (Chromodoris zebra).

Taylor; J.gen.Physiol.; vol. 11; p. 211; Chem. Zentralbl.; vol. 99; nb. I; (1928); p. 2409, View in Reaxys; Chozier; J.gen.Physiol.; vol. 5; p. 66; Chem. Zentralbl.; vol. 94; nb. I; (1923); p. 255, View in Reaxys 33 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 18.2 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

pyridine

Yajnik et al.; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 118; (1925); p. 312, View in Reaxys 34 of 43

Description (Transport Phenomena (MCS))

Viscosity

178/428

2017-08-01 04:43:04

Temperature (Transport 30 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

pyridine

Yajnik et al.; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 118; (1925); p. 312, View in Reaxys 35 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 40 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

pyridine

Yajnik et al.; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 118; (1925); p. 312, View in Reaxys 36 of 43

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

H2O

Comment (Transport Phenomena (MCS))

in Gelatine- und Eiweiss-Gele.

Traube; Yumikura; Biochemische Zeitschrift; vol. 157; (1925); p. 383, View in Reaxys; Yumikura; Biochemische Zeitschrift; vol. 157; (1925); p. 365, View in Reaxys; Traube; Biochemische Zeitschrift; vol. 153; (1924); p. 359, View in Reaxys; Tomita; Biochemische Zeitschrift; vol. 153; (1924); p. 349, View in Reaxys 37 of 43

Description (Transport Phenomena (MCS))

Viscosity

Partner (Transport Phenomena (MCS))

water

Pound; Russell; Journal of the Chemical Society; vol. 125; (1924); p. 780, View in Reaxys 38 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 30 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

aniline

Pound; Russell; Journal of the Chemical Society; vol. 125; (1924); p. 780, View in Reaxys 39 of 43

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 30 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

aniline; water

Pound; Russell; Journal of the Chemical Society; vol. 125; (1924); p. 780, View in Reaxys 40 of 43

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

H2O

Comment (Transport Phenomena (MCS))

durch lipoidhaltige Kollodium-Membrane.

Phillipson; Hannevart; C.r.Soc.Biol.; vol. 83; p. 1571; Chem. Zentralbl.; vol. 92; nb. I; (1921); p. 543, View in Reaxys 41 of 43

Description (Transport Phenomena (MCS))

Viscosity

179/428

2017-08-01 04:43:04

Partner (Transport Phenomena (MCS))

formamide

Merry; Turner; Journal of the Chemical Society; vol. 105; (1914); p. 758, View in Reaxys 42 of 43

Description (Transport Phenomena (MCS))

Viscosity

Solvent (Transport Phenomena (MCS))

H2O

Temperature (Transport 25 Phenomena (MCS)) [°C] Wilsdon; Sidgwick; Journal of the Chemical Society; vol. 103; (1913); p. 1965, View in Reaxys 43 of 43

Description (Transport Phenomena (MCS))

Viscosity

Solvent (Transport Phenomena (MCS))

H2O

Tsakalotos; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 146; (1908); p. 1147,1272, View in Reaxys; Traube,I.; Chemische Berichte; vol. 19; (1886); p. 885, View in Reaxys Triple Point (1) Triple Point [°C] -5.12

References Martin, J. F.; Andon, R. J. L.; Journal of Chemical Thermodynamics; vol. 14; nb. 7; (1982); p. 679 - 688, View in Reaxys

Vapour Pressure (20) Vapour Pressure Temperature (Va[Torr] pour Pressure) [°C]

Comment (Vapour Pressure)

References

0.540054

20.13

Negadi, Latifa; Mokbel, Ilham; Negadi, Amina; Kaci, Ahmed Ait; Jose, Jacques; Gmehling, Juergen; Journal of Chemical and Engineering Data; vol. 54; nb. 7; (2009); p. 2045 - 2048, View in Reaxys

0.789079

25.09

Negadi, Latifa; Mokbel, Ilham; Negadi, Amina; Kaci, Ahmed Ait; Jose, Jacques; Gmehling, Juergen; Journal of Chemical and Engineering Data; vol. 54; nb. 7; (2009); p. 2045 - 2048, View in Reaxys

1.15887

30.12

Negadi, Latifa; Mokbel, Ilham; Negadi, Amina; Kaci, Ahmed Ait; Jose, Jacques; Gmehling, Juergen; Journal of Chemical and Engineering Data; vol. 54; nb. 7; (2009); p. 2045 - 2048, View in Reaxys

2.36649

40.06

Negadi, Latifa; Mokbel, Ilham; Negadi, Amina; Kaci, Ahmed Ait; Jose, Jacques; Gmehling, Juergen; Journal of Chemical and Engineering Data; vol. 54; nb. 7; (2009); p. 2045 - 2048, View in Reaxys

4.63771

50.04

Negadi, Latifa; Mokbel, Ilham; Negadi, Amina; Kaci, Ahmed Ait; Jose, Jacques; Gmehling, Juergen; Journal of Chemical and Engineering Data; vol. 54; nb. 7; (2009); p. 2045 - 2048, View in Reaxys

8.65137

60.02

Negadi, Latifa; Mokbel, Ilham; Negadi, Amina; Kaci, Ahmed Ait; Jose, Jacques; Gmehling, Juergen; Journal of Chemical and Engineering Data; vol. 54; nb. 7; (2009); p. 2045 - 2048, View in Reaxys

15.5521

70.02

Negadi, Latifa; Mokbel, Ilham; Negadi, Amina; Kaci, Ahmed Ait; Jose, Jacques; Gmehling, Juergen; Journal of Chemical and Engineering Data; vol. 54; nb. 7; (2009); p. 2045 - 2048, View in Reaxys

26.8662

79.94

Negadi, Latifa; Mokbel, Ilham; Negadi, Amina; Kaci, Ahmed Ait; Jose, Jacques; Gmehling, Juergen; Journal of Chemical and Engineering Data; vol. 54; nb. 7; (2009); p. 2045 - 2048, View in Reaxys

44.8035

89.92

Negadi, Latifa; Mokbel, Ilham; Negadi, Amina; Kaci, Ahmed Ait; Jose, Jacques; Gmehling, Juergen; Journal of Chemical and Engineering Data; vol. 54; nb. 7; (2009); p. 2045 - 2048, View in Reaxys

1.12511

Trabue, Steven L.; Scoggin, Kenwood D.; Li, Hong; Burns, Robert; Xin, Hongwei; Environmental Science and Technology; vol. 42; nb. 10; (2008); p. 3745 - 3750, View in Reaxys

70.357 - 343.909

100 - 140

Giles, Neil F.; Wilson, Grant M.; Journal of Chemical and Engineering Data; vol. 51; nb. 6; (2006); p. 1966 - 1972, View in Reaxys

180/428

2017-08-01 04:43:04

109.209 - 750.36

110.4 - 162.9

Clifford, Scott L.; Ramjugernath, Deresh; Raal, J. David; Journal of Chemical and Engineering Data; vol. 49; nb. 5; (2004); p. 1189 1192, View in Reaxys

156.162 599.973

118.35 - 155.75

Munoz, Laura A. L.; Kraehenbuehl, M. Alvina; Journal of Chemical and Engineering Data; vol. 46; nb. 1; (2001); p. 120 - 124, View in Reaxys

0.200191 2.29068

5.05 - 34.95

166.363 589.397

120 - 155

Equation: ln(p/ Pa)=28.58-7036( T/K)-1

Verevkin; Journal of Chemical and Engineering Data; vol. 45; nb. 5; (2000); p. 953 - 960, View in Reaxys Zudkevitch; Lindrud; Chu; Journal of Chemical and Engineering Data; vol. 44; nb. 3; (1999); p. 393 - 397, View in Reaxys

Equation: ln(p/ kPa)=15.09674-3 599.963/ <T-93.307>

Miyamoto, Shinji; Nakamura, Shinichi; Iwai, Yoshio; Arai, Yasuhiko; Journal of Chemical and Engineering Data; vol. 44; nb. 1; (1999); p. 48 - 51, View in Reaxys

Equation: 2 equa- Ambrose, D.; Ghiassee, N. B.; Journal of Chemical Thermodynamtions ics; vol. 19; nb. 5; (1987); p. 505 - 520, View in Reaxys 22.0443 - 1182.8

76.5 - 178.9

Table exists. Ambrose, D.; Ellender, J. H.; Gundry, H. A.; Lee, D. A.; TownEquation: 2 equa- send, R.; Journal of Chemical Thermodynamics; vol. 13; nb. 8; tions (1981); p. 795 - 802, View in Reaxys Apelblat, Kohler; Journal of Chemical Thermodynamics; vol. 8; (1976); p. 749,751, 752, 754, 755, View in Reaxys; Wright; Akhtar; Journal of the Chemical Society [Section] B: Physical Organic; (1970); p. 151,152-153, View in Reaxys

15 - 40

equation exists.

Skljarenko et al.; Zhurnal Fizicheskoi Khimii; vol. 32; (1958); p. 692,695; Chem.Abstr.; (1958); p. 14266, View in Reaxys

NMR Spectroscopy (73) 1 of 73

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- d(4)-methanol; water-d2 scopy) Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectroscopy) [MHz]

400

Soares, Ana M.S.; Hungerford, Graham; Costa, Susana P.G.; Gonçalves, M. Sameiro T.; Dyes and Pigments; vol. 137; (2017); p. 91 - 100, View in Reaxys 2 of 73

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Mondal, Monohar Hossain; Malik, Susanta; De, Sourav; Bhattacharyya, Subhendu Sekhar; Saha, Bidyut; Research on Chemical Intermediates; vol. 43; nb. 3; (2017); p. 1651 - 1670, View in Reaxys 3 of 73

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- dimethylsulfoxide-d6 scopy)

181/428

2017-08-01 04:43:04

Frequency (NMR Spectroscopy) [MHz]

500

Location

supporting information

Yu, Han; Ru, Shi; Dai, Guoyong; Zhai, Yongyan; Lin, Hualin; Han, Sheng; Wei, Yongge; Angewandte Chemie International Edition; vol. 56; nb. 14; (2017); p. 3867 - 3871; Angew. Chem.; vol. 129; nb. 14; (2017); p. 3925 3929,5, View in Reaxys 4 of 73

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- dimethylsulfoxide-d6 scopy) Frequency (NMR Spectroscopy) [MHz]

125

Location

supporting information

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

500

Malik, Susanta; Ghosh, Aniruddha; Saha, Bidyut; Journal of Solution Chemistry; vol. 45; nb. 1; (2016); p. 109 125, View in Reaxys 6 of 73

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- aq. buffer; water-d2 scopy) Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectroscopy) [MHz]

500

Location

supporting information

Kamatham, Nareshbabu; Mendes, Débora C.; Da Silva, José P.; Givens, Richard S.; Ramamurthy; Organic Letters; vol. 18; nb. 21; (2016); p. 5480 - 5483, View in Reaxys 7 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Location

supporting information

Britton, Joshua; Chalker, Justin M.; Raston, Colin L.; Chemistry - A European Journal; vol. 21; nb. 30; (2015); p. 10660 - 10665, View in Reaxys 8 of 73

Description (NMR Spec- HSQC (Heteronuclear Single Quantum Coherence) troscopy)

182/428

2017-08-01 04:43:04

Nucleus (NMR Spectroscopy)

1H; 13C

Solvents (NMR Spectro- water-d2 scopy) Alves Filho, Elenilson G.; Sartori, Luci; Silva, Lorena M. A.; Silva, Bianca F.; Fadini, Pedro S.; Soong, Ronald; Simpson, Andre; Ferreira, Antonio G.; Magnetic Resonance in Chemistry; vol. 53; nb. 9; (2015); p. 704 - 710, View in Reaxys 9 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectroscopy) [MHz]

400

Soares, Ana M. S.; Hungerford, Graham; Costa, Susana P. G.; Gonçalves, M. Sameiro T.; New Journal of Chemistry; vol. 39; nb. 9; (2015); p. 7227 - 7233, View in Reaxys 10 of 73

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- d(4)-methanol; water-d2 scopy) Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectroscopy) [MHz]

400

Soares, Ana M. S.; Hungerford, Graham; Costa, Susana P. G.; Gonçalves, M. Sameiro T.; European Journal of Organic Chemistry; vol. 2015; nb. 27; (2015); p. 5979 - 5986, View in Reaxys 11 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- water-d2 scopy) Sreekantan, Smitha Velayuthan; Mahadevan, Surianarayanan; Jala, Samuel Vara Kumar; Seshadri, Hariharan; Mandal, Asit Baran; Organic Process Research and Development; vol. 18; nb. 12; (2014); p. 1821 - 1827, View in Reaxys 12 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy)

183/428

2017-08-01 04:43:04

Temperature (NMR Spectroscopy) [°C]

29.84

Glaszczka, Rafal; Jazwinski, Jaroslaw; Journal of Molecular Structure; vol. 1036; (2013); p. 78 - 89, View in Reaxys 14 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

29.84

Glaszczka, Rafal; Jazwinski, Jaroslaw; Journal of Molecular Structure; vol. 1036; (2013); p. 78 - 89, View in Reaxys 15 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- tetradeuterioacetic acid scopy) Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Coskun, Timur; Conifer, Christopher M.; Stevenson, Laura C.; Britovsek, George J. P.; Chemistry - A European Journal; vol. 19; nb. 21; (2013); p. 6840 - 6844, View in Reaxys 16 of 73

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Original Text (NMR Spectroscopy)

NMR (400 MHz, CDCl3): δ 0.87-0.97 (3H, m), 1.58-1.70 (2H, m), 2.29-2.35 (2H, q, J 7.2, 4.2 Hz), 11.0 (1H, br s)

Location

supporting information

Signals [ppm]

0.87 - 0.97; 1.58 - 1.7; 2.29 - 2.35; 11

Kind of signal

3H, m; 2H, m; 2H, q, J 7.2, 4.2 Hz; 1H, br s

Shaikh, Tanveer Mahammadali; Hong, Fung-E; Tetrahedron; vol. 69; nb. 42; (2013); p. 8929 - 8935, View in Reaxys 17 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Original Text (NMR Spectroscopy)

13C

NMR (100 MHz, CDCl3): δ 13.4, 18.0, 35.9, 180.3

184/428

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Signals [ppm]

13.4; 18; 35.9; 180.3

Shaikh, Tanveer Mahammadali; Hong, Fung-E; Tetrahedron; vol. 69; nb. 42; (2013); p. 8929 - 8935, View in Reaxys 18 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Rao, Gopal Krishna; Gowda, Narendra B.; Ramakrishna, Ramesha A.; Synthetic Communications; vol. 42; nb. 6; (2012); p. 893 - 904, View in Reaxys 19 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Rao, Gopal Krishna; Gowda, Narendra B.; Ramakrishna, Ramesha A.; Synthetic Communications; vol. 42; nb. 6; (2012); p. 893 - 904, View in Reaxys 20 of 73

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

Kunishima, Munetaka; Ujigawa, Takae; Nagaoka, Yoshie; Kawachi, Chiho; Hioki, Kazuhito; Shiro, Motoo; Chemistry - A European Journal; vol. 18; nb. 49; (2012); p. 15856 - 15867, View in Reaxys 21 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- dimethylsulfoxide-d6 scopy) Location

supporting information

Sodhi, Ravinderpal Kour; Paul, Satya; Clark; Green Chemistry; vol. 14; nb. 6; (2012); p. 1649 - 1656, View in Reaxys 22 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- dimethylsulfoxide-d6 scopy) Location

supporting information

Sodhi, Ravinderpal Kour; Paul, Satya; Clark; Green Chemistry; vol. 14; nb. 6; (2012); p. 1649 - 1656, View in Reaxys 23 of 73

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

185/428

2017-08-01 04:43:04

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Bonaparte, Amy C.; Betush, Matthew P.; Panseri, Bettina M.; Mastarone, Daniel J.; Murphy, Ryan K.; Murphree, S. Shaun; Organic Letters; vol. 13; nb. 6; (2011); p. 1447 - 1449, View in Reaxys 24 of 73

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Location

supporting information

Bonaparte, Amy C.; Betush, Matthew P.; Panseri, Bettina M.; Mastarone, Daniel J.; Murphy, Ryan K.; Murphree, S. Shaun; Organic Letters; vol. 13; nb. 6; (2011); p. 1447 - 1449, View in Reaxys 25 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Shaikh, Tanveer Mahamadali; Hong, Fung-E; Advanced Synthesis and Catalysis; vol. 353; nb. 9; (2011); p. 1491 1496, View in Reaxys 26 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Location

supporting information

Shaikh, Tanveer Mahamadali; Hong, Fung-E; Advanced Synthesis and Catalysis; vol. 353; nb. 9; (2011); p. 1491 1496, View in Reaxys 27 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Dintzner, Matthew R.; Mondjinou, Yawo A.; Pileggi, Dominic J.; Tetrahedron Letters; vol. 51; nb. 5; (2010); p. 826 - 827, View in Reaxys 28 of 73

Description (NMR Spec- Chemical shifts troscopy)

186/428

2017-08-01 04:43:04

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

Dintzner, Matthew R.; Mondjinou, Yawo A.; Pileggi, Dominic J.; Tetrahedron Letters; vol. 51; nb. 5; (2010); p. 826 - 827, View in Reaxys 29 of 73

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Location

supporting information

Malik, Payal; Chakraborty, Debashis; Tetrahedron Letters; vol. 51; nb. 27; (2010); p. 3521 - 3523, View in Reaxys 30 of 73

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Location

supporting information

Malik, Payal; Chakraborty, Debashis; Tetrahedron Letters; vol. 51; nb. 27; (2010); p. 3521 - 3523, View in Reaxys 31 of 73

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Location

supporting information

Malik, Payal; Chakraborty, Debashis; Synthesis; nb. 21; (2010); p. 3736 - 3740; Art.No: Z17610SS, View in Reaxys 32 of 73

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Location

supporting information

Malik, Payal; Chakraborty, Debashis; Synthesis; nb. 21; (2010); p. 3736 - 3740; Art.No: Z17610SS, View in Reaxys 33 of 73

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Arivazhagan; Parthipan; Thenappan; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 74; nb. 4; (2009); p. 860 - 868, View in Reaxys 34 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy)

187/428

2017-08-01 04:43:04

Frequency (NMR Spectroscopy) [MHz]

Katritzky, Alan R.; Singh, Sandeep K.; Jiang, Rong; Tetrahedron; vol. 62; nb. 16; (2006); p. 3794 - 3797, View in Reaxys; Baloch, Imam Bakhsh; Baloch, Musa Kaleem; Saqib, Qazi Najam us; European Journal of Medicinal Chemistry; vol. 43; nb. 2; (2008); p. 274 - 281, View in Reaxys 35 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Webb, Kevin S.; Ruszkay, Stephen J.; Tetrahedron; vol. 54; nb. 3-4; (1998); p. 401 - 410, View in Reaxys; Katritzky, Alan R.; Singh, Sandeep K.; Jiang, Rong; Tetrahedron; vol. 62; nb. 16; (2006); p. 3794 - 3797, View in Reaxys; Baloch, Imam Bakhsh; Baloch, Musa Kaleem; Saqib, Qazi Najam us; European Journal of Medicinal Chemistry; vol. 43; nb. 2; (2008); p. 274 - 281, View in Reaxys 36 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

500

Niu, Dong-Fang; Xiao, Li-Ping; Zhang, Ai-Jian; Zhang, Gui-Rong; Tan, Qi-Yun; Lu, Jia-Xing; Tetrahedron; vol. 64; nb. 46; (2008); p. 10517 - 10520, View in Reaxys 37 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Zara, Cynthia Lynn; Jin, Thomas; Giguere, Raymond J.; Synthetic Communications; vol. 30; nb. 12; (2000); p. 2099 - 2104, View in Reaxys; Niu, Dong-Fang; Xiao, Li-Ping; Zhang, Ai-Jian; Zhang, Gui-Rong; Tan, Qi-Yun; Lu, Jia-Xing; Tetrahedron; vol. 64; nb. 46; (2008); p. 10517 - 10520, View in Reaxys 38 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- water-d2 scopy) Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectroscopy) [MHz]

400

Schripsema, Jan; Journal of Agricultural and Food Chemistry; vol. 56; nb. 8; (2008); p. 2547 - 2552, View in Reaxys 39 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Belokon, Yuri N.; Pritula, Ludmila K.; Tararov, Vitali I.; Bakhmutov, Vladimir I.; Gusev, Dimitri G.; et al.; Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999); nb. 6; (1990); p. 1873 - 1877,

188/428

2017-08-01 04:43:04

View in Reaxys; Becker, James Y.; Zinger, Baruch; Yatziv, Shimon; Journal of Organic Chemistry; vol. 52; nb. 13; (1987); p. 2783 - 2789, View in Reaxys; Metsger, Leonid; Bittner, Shmuel; Tetrahedron; vol. 56; nb. 13; (2000); p. 1905 - 1910, View in Reaxys; Kirillova, Marina V.; Da Silva, Jose A. L.; Da Silva, Joao J. R. Frausto; Palavra, Antonio F.; Pombeiro, Armando J. L.; Advanced Synthesis and Catalysis; vol. 349; nb. 10; (2007); p. 1765 - 1774, View in Reaxys 40 of 73

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

400.13

Abraham, Raymond J.; Byrne, Jonathan J.; Griffiths, Lee; Perez, Manuel; Magnetic Resonance in Chemistry; vol. 44; nb. 5; (2006); p. 491 - 509, View in Reaxys 42 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- dimethylsulfoxide-d6 scopy) Frequency (NMR Spectroscopy) [MHz]

400.13

Abraham, Raymond J.; Byrne, Jonathan J.; Griffiths, Lee; Perez, Manuel; Magnetic Resonance in Chemistry; vol. 44; nb. 5; (2006); p. 491 - 509, View in Reaxys 43 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- acetone-d6 scopy) Frequency (NMR Spectroscopy) [MHz]

500

Velayutham; Jayaraman; Kulangiappar; Ilayaraja; Babu, Y. Ram; Rao, P. Santhan; Reddy, S. Narayana; Babu, K. Victor; Noel; Journal of Fluorine Chemistry; vol. 127; nb. 8; (2006); p. 1111 - 1118, View in Reaxys 44 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- D2O; CD3CN scopy) Frequency (NMR Spectroscopy) [MHz]

500

Somers, Neil A.; Kazlauskas, Romas J.; Tetrahedron Asymmetry; vol. 15; nb. 18; (2004); p. 2991 - 3004, View in Reaxys

189/428

2017-08-01 04:43:04

45 of 73

Description (NMR Spec- Spin-spin relaxation time (T2) troscopy) Nucleus (NMR Spectroscopy)

Ellis, David A.; Denkenberger, Kerri A.; Burrow, Timothy E.; Mabury, Scott A.; Journal of Physical Chemistry A; vol. 108; nb. 46; (2004); p. 10099 - 10106, View in Reaxys 46 of 73

Description (NMR Spec- Spin-lattice relaxation time (T1) troscopy) Nucleus (NMR Spectroscopy)

Ellis, David A.; Denkenberger, Kerri A.; Burrow, Timothy E.; Mabury, Scott A.; Journal of Physical Chemistry A; vol. 108; nb. 46; (2004); p. 10099 - 10106, View in Reaxys 47 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- D2O scopy) Frequency (NMR Spectroscopy) [MHz]

Comment (NMR Spectroscopy)

pH dependence

Panyushkin; Sukhno; Vodopetova; Russian Journal of General Chemistry; vol. 73; nb. 4; (2003); p. 507 - 510, View in Reaxys 48 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

200

Zara, Cynthia Lynn; Jin, Thomas; Giguere, Raymond J.; Synthetic Communications; vol. 30; nb. 12; (2000); p. 2099 - 2104, View in Reaxys 49 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3; CHCl3 scopy) Temperature (NMR Spectroscopy) [°C]

O'Connor, Charmian J.; Barton, Richard H.; Australian Journal of Chemistry; vol. 52; nb. 2; (1999); p. 123 - 127, View in Reaxys 50 of 73

Description (NMR Spec- Spin-lattice relaxation time (T1) troscopy) Deshmukh et al.; Molecular Physics; vol. 36; (1978); p. 1721,1722,1724,1728, View in Reaxys; Johns et al.; Australian Journal of Chemistry; vol. 30; (1977); p. 813,816, View in Reaxys; Miller et al.; Journal of the Chemical Society, Chemical Communications; (1979); p. 758, View in Reaxys; Belokon, Yuri N.; Pritula, Ludmila K.; Tararov, Vitali I.; Bakhmutov, Vladimir I.; Gusev, Dimitri G.; et al.; Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999); nb. 6; (1990); p. 1873 - 1877, View in Reaxys; Gutsche, C. David; See, Keat Aun; Journal of Organic Chemistry; vol. 57; nb. 16; (1992); p. 4527 - 4539, View in Reaxys

51 of 73

Description (NMR Spec- Chemical shifts troscopy)

190/428

2017-08-01 04:43:04

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CCl4 scopy) Kawashima, Masatoshi; Sato, Toshio; Fujisawa, Tamotsu; Tetrahedron; vol. 45; nb. 2; (1989); p. 403 - 412, View in Reaxys 52 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- HBr; various solvent(s) scopy) Temperature (NMR Spectroscopy) [°C]

-125.2 - -105.2

Clark, David R.; Emsley, John; Hibbert, Frank; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1989); p. 1455 - 1458, View in Reaxys 53 of 73

Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- CCl4 scopy) Comment (NMR Spectroscopy)

1H-1H

Kawashima, Masatoshi; Sato, Toshio; Fujisawa, Tamotsu; Tetrahedron; vol. 45; nb. 2; (1989); p. 403 - 412, View in Reaxys 54 of 73

Description (NMR Spec- Linewidth of NMR absorption troscopy) Clark, David R.; Emsley, John; Hibbert, Frank; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1989); p. 1455 - 1458, View in Reaxys; Delseth, Claude; Nguyen, Thi ThanhTam; Kintzinger, Jean-Pierre; Helvetica Chimica Acta; vol. 63; nb. 2; (1980); p. 498 - 503, View in Reaxys

55 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- D2O scopy) Colucci, William J.; Gandour, Richard D.; Mooberry, Edward A.; Journal of the American Chemical Society; vol. 108; nb. 23; (1986); p. 7141 - 7147, View in Reaxys 56 of 73

Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- D2O scopy) Comment (NMR Spectroscopy)

1H-1H

Colucci, William J.; Gandour, Richard D.; Mooberry, Edward A.; Journal of the American Chemical Society; vol. 108; nb. 23; (1986); p. 7141 - 7147, View in Reaxys 57 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Temperature (NMR Spectroscopy) [°C]

191/428

2017-08-01 04:43:04

Takeuchi, Yoshito; Tomoda, Shuji; Kakimoto, Norihiro; Magnetic Resonance in Chemistry; vol. 23; nb. 2; (1985); p. 140 - 143, View in Reaxys 58 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

17O

Temperature (NMR Spectroscopy) [°C]

Gerothanassis, Ioannis P.; Hunston, Roger N.; Lauterwein, Juergen; Magnetic Resonance in Chemistry; vol. 23; nb. 8; (1985); p. 659 - 665, View in Reaxys 59 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Temperature (NMR Spectroscopy) [°C]

Ejchart, Andrzej; Polish Journal of Chemistry; vol. 55; nb. 5; (1981); p. 1169 - 1175, View in Reaxys; Ejchart, Andrzej; Organic Magnetic Resonance; vol. 13; nb. 5; (1980); p. 368 - 371, View in Reaxys 60 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3; CCl4 scopy) Delseth, Claude; Nguyen, Thi Thanh-Tam; Kintzinger, Jean-Pierre; Helvetica Chimica Acta; vol. 63; nb. 2; (1980); p. 498 - 503, View in Reaxys 61 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectro- neat (no solvent) scopy) Temperature (NMR Spectroscopy) [°C]

Delseth, Claude; Nguyen, Thi Thanh-Tam; Kintzinger, Jean-Pierre; Helvetica Chimica Acta; vol. 63; nb. 2; (1980); p. 498 - 503, View in Reaxys 62 of 73

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- D2O scopy) Temperature (NMR Spectroscopy) [°C]

34.1

Dillon, K. B.; Harrison, M. R.; Rossotti, F. J. C.; Journal of Magnetic Resonance (1969-1992); vol. 39; nb. 3; (1980); p. 499 - 508, View in Reaxys 63 of 73

Description (NMR Spec- NOE troscopy) Miller et al.; Journal of the Chemical Society, Chemical Communications; (1979); p. 758, View in Reaxys

64 of 73

Description (NMR Spec- NMR troscopy)

192/428

2017-08-01 04:43:04

Hagen,R.; Roberts,J.D.; Journal of the American Chemical Society; vol. 91; (1969); p. 4504 - 4506, View in Reaxys; Morishima,I. et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 2749 - 2756, View in Reaxys; Lancelot,G. et al.; Journal of the American Chemical Society; vol. 101; (1979); p. 1569 - 1576, View in Reaxys; Kofron,W.G.; Wideman,L.G.; Journal of Organic Chemistry; vol. 37; (1972); p. 555 - 559, View in Reaxys; Marshall,J.L.; Miller,D.E.; Journal of the American Chemical Society; vol. 95; (1973); p. 8305, View in Reaxys; Kawazoe; Ohnishi; Chemical and Pharmaceutical Bulletin; vol. 11; (1963); p. 243,245, View in Reaxys; Cavanaugh; Dailey; Journal of Chemical Physics; vol. 34; (1961); p. 1099,1100, View in Reaxys; Miyazima et al.; Journal of Physical Chemistry; vol. 73; (1969); p. 1370, View in Reaxys; Noble et al.; Journal of Physical Chemistry; vol. 66; (1962); p. 1188, View in Reaxys; Stothers; Lauterbur; Canadian Journal of Chemistry; vol. 42; (1964); p. 1563,1572, View in Reaxys; Marr; Stothers; Canadian Journal of Chemistry; vol. 45; (1967); p. 225,228, View in Reaxys; Batchelor et al.; Journal of Magnetic Resonance (1969-1992); vol. 20; (1975); p. 19, View in Reaxys; Williamson et al.; Journal of Magnetic Resonance (1969-1992); vol. 30; (1978); p. 367,372, View in Reaxys; Couperus et al.; Organic Magnetic Resonance; vol. 11; (1978); p. 590,595, View in Reaxys; Terent'ev et al.; Organic Magnetic Resonance; vol. 9; (1977); p. 301, View in Reaxys; Kimtys; Spectroscopy Letters; vol. 10; (1977); p. 43,46, View in Reaxys; Johns et al.; Australian Journal of Chemistry; vol. 30; (1977); p. 813,816, View in Reaxys; Engelhardt et al.; Journal fuer Praktische Chemie (Leipzig); vol. 312; (1970); p. 935,942, View in Reaxys; Horsley; Sternlicht; Journal of the American Chemical Society; vol. 90; nb. 14; (1968); p. 3738 3748, View in Reaxys 65 of 73

Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)

13C

chemical shifts (Table 3)

Rabenstein; Sayer; Journal of Magnetic Resonance (1969-1992); vol. 24; (1976); p. 27, View in Reaxys 66 of 73

Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)

1H (-COOH); Vgl. m. and. Carbonsaeuren, Zusammenhang m. Struktur u. Reaktivitaet

Rybakov et al.; Russian Journal of Physical Chemistry; vol. 49; (1975); p. 441; ; p. 756, View in Reaxys 67 of 73

Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)

carbon-13 chemical shifts

Yonemoto,T.; Journal of Magnetic Resonance (1969-1992); vol. 13; (1974); p. 153, View in Reaxys 68 of 73

Description (NMR Spec- Spin-spin coupling constants troscopy) Marshall,J.L.; Miller,D.E.; Journal of the American Chemical Society; vol. 95; (1973); p. 8305, View in Reaxys

69 of 73

Description (NMR Spec- Chemical shifts troscopy) Silver et al.; Journal of Physical Chemistry; vol. 70; (1966); p. 1434,1436, View in Reaxys

70 of 73

Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)

wss. Lsgg. versch. Konz. bei 36grad

Rueterjans; Scheraga; Journal of Chemical Physics; vol. 45; (1966); p. 3296, View in Reaxys 71 of 73

Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)

17O-NMR-Linien

Christ et al.; Helvetica Chimica Acta; vol. 44; (1961); p. 865, View in Reaxys 72 of 73

Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)

1H, in Bzl., versch. Konz.

Shimizu; Nippon Kagaku Zasshi; vol. 81; (1960); p. 1025; Chem.Abstr.; nb. 22021; (1960), View in Reaxys

193/428

2017-08-01 04:43:04

73 of 73

Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)

1H, in Py., versch. Konz.

Shimizu; Nippon Kagaku Zasshi; vol. 81; (1960); p. 1025; Chem.Abstr.; nb. 22021; (1960), View in Reaxys IR Spectroscopy (35) 1 of 35

Description (IR Spectroscopy)

Bands; Spectrum

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

Sreekantan, Smitha Velayuthan; Mahadevan, Surianarayanan; Jala, Samuel Vara Kumar; Seshadri, Hariharan; Mandal, Asit Baran; Organic Process Research and Development; vol. 18; nb. 12; (2014); p. 1821 - 1827, View in Reaxys; Zhu, Wenshuai; Wang, Chao; Li, Hongping; Wu, Peiwen; Xun, Suhang; Jiang, Wei; Chen, Zhigang; Zhao, Zhen; Li, Huaming; Green Chemistry; vol. 17; nb. 4; (2015); p. 2464 - 2472, View in Reaxys 2 of 35

Description (IR Spectroscopy)

Bands; Spectrum

Temperature (IR Spectroscopy) [°C]

24.99

Sekhar, M. Chandra; Venkatesulu; Mohan, T. Madhu; Gowrisankar; Oriental Journal of Chemistry; vol. 31; nb. 2; (2015); p. 897 - 906, View in Reaxys 3 of 35

Description (IR Spectroscopy)

Bands

Location

supporting information

Sodhi, Ravinderpal Kour; Paul, Satya; Clark; Green Chemistry; vol. 14; nb. 6; (2012); p. 1649 - 1656, View in Reaxys; McEntee, Monica; Tang, Wenjie; Neurock, Matthew; Yates, John T.; Journal of the American Chemical Society; vol. 136; nb. 13; (2014); p. 5116 - 5120, View in Reaxys 4 of 35

Description (IR Spectroscopy)

Bands; Spectrum

Temperature (IR Spectroscopy) [°C]

Arivazhagan; Shanmugam; Elangovan; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 105; (2013); p. 102 - 108, View in Reaxys 5 of 35

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

neat liquid

Rao, Gopal Krishna; Gowda, Narendra B.; Ramakrishna, Ramesha A.; Synthetic Communications; vol. 42; nb. 6; (2012); p. 893 - 904, View in Reaxys 6 of 35

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

Shaikh, Tanveer Mahamadali; Hong, Fung-E; Advanced Synthesis and Catalysis; vol. 353; nb. 9; (2011); p. 1491 1496, View in Reaxys 7 of 35

Description (IR Spectroscopy)

Bands

Josien et al.; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 250; (1960); p. 4146, View in Reaxys; Satchell; Wardell; Transactions of the Faraday Society; vol. 61; (1965); p. 1199, View in Reaxys; Katon et al.; Applied Spectroscopy; vol. 25; (1971); p. 497, View in Reaxys; Gotoh; Takenaka; Nippon Kagaku Zasshi; vol. 81; (1960); p. 1504,1505; Chem.Abstr.; nb. 3136; (1961), View in Reaxys; Kawano; Nippon Kagaku Zasshi; vol. 81; (1960); p. 1652,1653; Chem.Abstr.; nb. 7040; (1961), View in Reaxys; Hayashi; Umemura; Journal of Chemical Physics; vol. 63; (1975); p. 1732,1735, View in Reaxys; Havey; Vaida; Journal of

194/428

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Molecular Spectroscopy; vol. 228; nb. 1; (2004); p. 152 - 159, View in Reaxys; Dintzner, Matthew R.; Mondjinou, Yawo A.; Pileggi, Dominic J.; Tetrahedron Letters; vol. 51; nb. 5; (2010); p. 826 - 827, View in Reaxys 8 of 35

Description (IR Spectroscopy)

Bands; Spectrum

Arivazhagan; Parthipan; Thenappan; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 74; nb. 4; (2009); p. 860 - 868, View in Reaxys 9 of 35

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

KBr

Bratulescu, George; Revue Roumaine de Chimie; vol. 50; nb. 3; (2005); p. 161 - 163, View in Reaxys 10 of 35

Description (IR Spectroscopy)

Intensity of near IR bands

Havey; Vaida; Journal of Molecular Spectroscopy; vol. 228; nb. 1; (2004); p. 152 - 159, View in Reaxys 11 of 35

Description (IR Spectroscopy)

Near IR bands

Comment (IR Spectroscopy)

ambient temperature

Havey; Vaida; Journal of Molecular Spectroscopy; vol. 228; nb. 1; (2004); p. 152 - 159, View in Reaxys 12 of 35

Description (IR Spectroscopy)

Near IR spectrum

Comment (IR Spectroscopy)

ambient temperature

Havey; Vaida; Journal of Molecular Spectroscopy; vol. 228; nb. 1; (2004); p. 152 - 159, View in Reaxys 13 of 35

Description (IR Spectroscopy)

Spectrum

Temperature (IR Spectroscopy) [°C]

24.85

Havey; Vaida; Journal of Molecular Spectroscopy; vol. 228; nb. 1; (2004); p. 152 - 159, View in Reaxys 14 of 35

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CHCl3

Chaubey, Girija S.; Das, Simi; Mahanti, Mahendra K.; Croatica Chemica Acta; vol. 76; nb. 4; (2003); p. 287 - 291, View in Reaxys 15 of 35

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

H2O

Comment (IR Spectroscopy)

3800 - 2800 cm**(-1)

Fischer; Eysel; Journal of Molecular Structure; vol. 415; nb. 3; (1997); p. 249 - 257, View in Reaxys 16 of 35

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

3100 - 1710 cm**(-1)

Kawashima, Masatoshi; Sato, Toshio; Fujisawa, Tamotsu; Tetrahedron; vol. 45; nb. 2; (1989); p. 403 - 412, View in Reaxys 17 of 35

Description (IR Spectroscopy)

Bands

195/428

2017-08-01 04:43:04

Comment (IR Spectroscopy)

3370 - 1730 cm**(-1)

Becker, James Y.; Zinger, Baruch; Yatziv, Shimon; Journal of Organic Chemistry; vol. 52; nb. 13; (1987); p. 2783 - 2789, View in Reaxys 18 of 35

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

gas

Comment (IR Spectroscopy)

3578 - 1782 cm**(-1)

Imre, L.; Danoczy, E.; Jalsovszky, G.; Holly S.; Journal of Molecular Structure; vol. 79; (1982); p. 35 - 38, View in Reaxys 19 of 35

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

4000 - 500 cm**(-1)

Lowry, Stephen R.; Huppler, David A.; Analytical Chemistry; vol. 53; nb. 6; (1981); p. 889 - 893, View in Reaxys 20 of 35

Description (IR Spectroscopy)

Spectrum

Jones; Canadian Journal of Chemistry; vol. 40; (1962); p. 321, View in Reaxys; Lorenzelli; Annali di Chimica (Rome, Italy); vol. 53; (1963); p. 1018,1020, View in Reaxys; Bentley et al.; Spectrochimica Acta; vol. 20; (1964); p. 685,688, View in Reaxys; Excoffon; Marechal; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 28; (1972); p. 269, View in Reaxys; Hill; Levin; Journal of Chemical Physics; vol. 70; (1979); p. 842, View in Reaxys 21 of 35

Description (IR Spectroscopy)

Jakobsen et al.; Spectrochimica Acta; vol. 25A; (1969); p. 839, View in Reaxys; Welti; Stephany; Applied Spectroscopy; vol. 22; (1968); p. 678,686, View in Reaxys; Fruwert et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 27; (1971); p. 1279, View in Reaxys; Saunders et al.; Applied Spectroscopy; vol. 22; (1968); p. 286,287, View in Reaxys; Le Fevre et al.; Australian Journal of Chemistry; vol. 19; (1966); p. 1325, View in Reaxys; Ivanchev et al.; Russian Journal of Physical Chemistry; vol. 39; (1965); p. 1009; ; p. 1900, View in Reaxys; Lascombe et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 59; (1962); p. 1233,1235, View in Reaxys; Paillous; Bulletin de la Societe Chimique de France; (1977); p. 415,418,419, View in Reaxys; Kuo; Chen; Journal of the Chinese Chemical Society (Taipei, Taiwan); vol. 23; (1976); p. 61, View in Reaxys; Glazunov et al.; Journal of Applied Spectroscopy; vol. 21; (1974); p. 936,937; ; p. 121, View in Reaxys; Bondarovich et al.; Journal of Agricultural and Food Chemistry; vol. 15; (1967); p. 36,45, View in Reaxys; Clemett; Journal of the Chemical Society [Section] D: Chemical Communications; (1970); p. 211, View in Reaxys; Macphee; Dubois; Tetrahedron Letters; (1978); p. 2225, View in Reaxys; Emsley; Hoyte; Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999); (1976); p. 2219, View in Reaxys 22 of 35

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

14286 - 667 cm**(-1)

Muecke et al.; Journal fuer Praktische Chemie (Leipzig); vol. <4>9; (1959); p. 16,18,22, View in Reaxys 23 of 35

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

1500 - 700 cm**(-1); Dampf.

Hadzi; Pintar; Spectrochimica Acta; vol. 12; (1958); p. 162,163, View in Reaxys 24 of 35

Description (IR Spectroscopy)

Spectrum

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Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

3500 - 670 cm**(-1)

Rigaux; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 238; (1954); p. 63,783, View in Reaxys; Corish; Chapman; Journal of the Chemical Society; (1957); p. 1746, View in Reaxys 25 of 35

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

5000 - 667 cm**(-1); Dampf.

Stephens et al.; Analytical Chemistry; vol. 29; (1957); p. 776, View in Reaxys 26 of 35

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

3500 - 670 cm**(-1); Kristalle.

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

CCl4

Comment (IR Spectroscopy)

3700 - 1500 cm**(-1)

Bratoz et al.; Spectrochimica Acta; vol. 8; (1956); p. 249,254, View in Reaxys 28 of 35

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

CCl4

Comment (IR Spectroscopy)

11111 - 3333 cm**(-1)

Holman; Edmondson; Analytical Chemistry; vol. 28; (1956); p. 1533, View in Reaxys 29 of 35

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

3700 - 1500 cm**(-1)

Bratoz et al.; Spectrochimica Acta; vol. 8; (1956); p. 249,254, View in Reaxys 30 of 35

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

3700 - 1500 cm**(-1); Kristalle.

Bratoz et al.; Spectrochimica Acta; vol. 8; (1956); p. 249,254, View in Reaxys 31 of 35

Description (IR Spectroscopy)

Spectrum

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Comment (IR Spectroscopy)

10000 - 769 cm**(-1); Dampf.

Herman; Journal of Chemical Physics; vol. 8; (1940); p. 256, View in Reaxys 32 of 35

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

11111 - 5556 cm**(-1); Fluessigkeit.

Errera; Mollet; Journal de Physique et le Radium; vol. <7>6; (1935); p. 287; Chem. Zentralbl.; vol. 107; nb. I; (1936); p. 2330, View in Reaxys; Freri; Anzi; Atti della Accademia Nazionale dei Lincei, Classe di Scienze Fisiche, Matematiche e Naturali, Rendiconti; vol. <7> 1; (1940); p. 367; Chem. Zentralbl.; vol. 111; nb. II; (1940); p. 3610, View in Reaxys 33 of 35

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

12500 - 5000 cm**(-1); ultrarotes Absorptionsspektrum.

Sappenfield; Physical Review; vol. <2>33; (1929); p. 40,42; Chem. Zentralbl.; vol. 100; nb. I; (1929); p. 1419, View in Reaxys 34 of 35

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

20000 - 714 cm**(-1); ultrarotes Absorptionsspektrum.

Weniger; Physical Review; vol. <1>31; (1910); p. 420 Tafel II, View in Reaxys 35 of 35

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

5000 - 667 cm**(-1)

A.P.I.; Res.Project 44 Nr.1227<1951>, View in Reaxys Mass Spectrometry (23) Description (Mass Location Spectrometry)

Comment (Mass Spectrometry)

References

gas chromatography mass spectrometry (GCMS); spectrum

Palencia, Gemma; Ibargoitia, Maria Luisa; Fresno, Maria; Sopelana, Patricia; Guillen, Maria Dolores; Molecules; vol. 19; nb. 6; (2014); p. 7937 - 7958, View in Reaxys; Palomero, Felipe; Bertani, Paolo; Fernández De Simón, Brígida; Cadahía, Estrella; Benito, Santiago; Morata, Antonio; Suárez-Lepe, José A.; Food Chemistry; vol. 171; (2014); p. 212 - 223, View in Reaxys; Roth; Meiringer; Kollmannsberger; Zarnkow; Jekle; Becker; Journal of Agricultural and Food Chemistry; vol. 62; nb. 45; (2014); p. 10873 - 10880, View in Reaxys; Kumari, Asha; Parida, Asish Kumar; RSC Advances; vol. 6; nb. 57; (2016); p. 51629 - 51641, View in Reaxys; Franitza, Laura; Granvogl, Michael; Schieberle, Peter; Journal of Agricultural and Food Chemistry; vol. 64; nb. 47; (2016); p. 9041 - 9053, View in Reaxys

electron impact (EI); gas chromatography mass spectrometry (GCMS); spectrum

Munafo, John P.; Didzbalis, John; Schnell, Raymond J.; Steinhaus, Martin; Journal of Agricultural and Food Chemistry; vol. 64; nb. 21; (2016); p. 4312 - 4318, View in Reaxys

CI (Chemical ionization); spectrum

Ortner, Eva; Granvogl, Michael; Schieberle, Peter; Journal of Agricultural and Food Chemistry; vol. 64; nb. 43; (2016); p. 8179 - 8190, View in Reaxys

electrospray ionisation (ESI); spectrum

Dong, Yu; Wang, Ziting; Yang, Xin; Zhu, Meiying; Chen, Rufen; Lu, Bin; Liu, Hui; RSC Advances; vol. 6; nb. 105; (2016); p. 102972 - 102978, View in Reaxys

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electrospray ionisation (ESI); liquid chromatography mass spectrometry (LCMS); spectrum

Munoz, Macarena; Domnguez, Carmen M.; De Pedro, Zahara M.; Quintanilla, Asuncin; Casas, Jose A.; Rodriguez, Juan J.; Catalysis Today; vol. 240; nb. PA; (2015); p. 16 - 21, View in Reaxys

spectrum

Pacholec, Frank; Eaton, David R.; Rossi, David T.; Analytical Chemistry; vol. 58; nb. 12; (1986); p. 2581 - 2583, View in Reaxys; McAdoo, David J.; Hudson, Charles E.; Griffin, Lawrence L.; Journal of Physical Chemistry; vol. 88; nb. 8; (1984); p. 1481 - 1485, View in Reaxys; Maccoll, Allan; Organic Mass Spectrometry; vol. 23; (1988); p. 381 - 387, View in Reaxys; Butler, James J.; FraserMonteiro, Maria L.; Fraser-Monteiro, Luis; Baer, Tomas; Hass, J. Ronald; Journal of Physical Chemistry; vol. 86; nb. 5; (1982); p. 747 - 752, View in Reaxys; Sakai, Kiyofumi; Hamada, Nobutake; Watanabe, Yasuto; Agricultural and Biological Chemistry; vol. 49; nb. 6; (1985); p. 1901 - 1902, View in Reaxys; Wood, William F.; Parker, Joshua M.; Weldon, Paul J.; Journal of Chemical Ecology; vol. 21; nb. 2; (1995); p. 213 - 220, View in Reaxys; Niu, Dong-Fang; Xiao, Li-Ping; Zhang, Ai-Jian; Zhang, Gui-Rong; Tan, Qi-Yun; Lu, JiaXing; Tetrahedron; vol. 64; nb. 46; (2008); p. 10517 - 10520, View in Reaxys; Rakete, Stefan; Berger, Robert; Böhme, Steffi; Glomb, Marcus A.; Journal of Agricultural and Food Chemistry; vol. 62; nb. 30; (2014); p. 7541 - 7549, View in Reaxys

gas chromatogra- Page/Page colphy mass specumn 32 trometry (GCMS); spectrum

Patent; Université de Lausanne; Broillet, Marie-Christine; Brechbühl, Julien; EP2772487; (2014); (A1) English, View in Reaxys

spectrum

supporting information

gas chromatography mass spectrometry (GCMS); electron impact (EI); spectrum

Park, Hye-Jung; Lee, Sang Mi; Song, Sang Hoon; Kim, YoungSuk; Molecules; vol. 18; nb. 5; (2013); p. 5317 - 5325, View in Reaxys

CI (Chemical ionization); Spectrum

Christlbauer, Monika; Schieberle, Peter; Journal of Agricultural and Food Chemistry; vol. 59; nb. 24; (2011); p. 13122 - 13130, View in Reaxys; Kawalec, Michal; Coulembier, Olivier; Gerbaux, Pascal; Sobota, Michal; De Winter, Julien; Dubois, Philippe; Kowalczuk, Marek; Kurcok, Piotr; Reactive and Functional Polymers; vol. 72; nb. 8; (2012); p. 509 - 520, View in Reaxys

electrospray ionisation (ESI); spectrum

supporting information

Sodhi, Ravinderpal Kour; Paul, Satya; Clark; Green Chemistry; vol. 14; nb. 6; (2012); p. 1649 - 1656, View in Reaxys

SIFT MS (selected ion flow tube mass spectrometry); Spectrum

Smith, David; Chippendale, Thomas W.E.; Spanel, Patrik; International Journal of Mass Spectrometry; vol. 303; nb. 2-3; (2011); p. 81 89, View in Reaxys

GCMS (Gas chromatography mass spectrometry); EI (Electron impact); Spectrum

Rodriguez-Bencomo, Juan J.; Cabrera-Valido, Hector M.; PerezTrujillo, Juan P.; Cacho, Juan; Food Chemistry; vol. 127; nb. 3; (2011); p. 1153 - 1162, View in Reaxys

APCI (atmospheric pressure chemical ionization); IT (ion trap); Spectrum

Habicht, Steve C.; Vinueza, Nelson R.; Amundson, Lucas M.; Kenttaemaa, Hilkka I.; Journal of the American Society for Mass Spectrometry; vol. 22; nb. 3; (2011); p. 520 - 530, View in Reaxys

GCMS (Gas chromatography mass

De Pinho, P. Guedes; Ribeiro, Barbara; Goncalves, Rui F.; Baptista, Paula; Valentao, Patricia; Seabra, Rosa M.; Andrade, Paula B.; Journal of Agricultural and Food Chemistry; vol. 56; nb. 5; (2008); p. 1704 - 1712, View in Reaxys

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spectrometry); Spectrum spectrum; chemical ionization (CI); ion-cyclotron resonance

Watkins, Michael A.; Price, Jason M.; Winger, Brian E.; Kenttaemaa, Hilkka I.; Analytical Chemistry; vol. 76; nb. 4; (2004); p. 964 976, View in Reaxys

spectrum; electron impact (EI)

Holmes, John L.; Lossing, F. P.; Journal of the American Chemical Society; vol. 102; nb. 11; (1980); p. 3732 - 3735, View in Reaxys; Becker, James Y.; Zinger, Baruch; Yatziv, Shimon; Journal of Organic Chemistry; vol. 52; nb. 13; (1987); p. 2783 - 2789, View in Reaxys

fragmentation pattern; spectrum

Maccoll, Allan; Organic Mass Spectrometry; vol. 21; (1986); p. 601 612, View in Reaxys

electron impact (EI); spectrum

Sakai, Kiyofumi; Hamada, Nobutake; Watanabe, Yasuto; Agricultural and Biological Chemistry; vol. 50; nb. 4; (1986); p. 989 - 996, View in Reaxys

fragmentation pattern; electron impact (EI); spectrum

Teleshefsky, L. A.; Jones, B. E.; Abbey, L. E.; Bostwick, D. E.; Burgess, E. M; Moran T. F.; Organic Mass Spectrometry; vol. 17; nb. 10; (1982); p. 481 - 492, View in Reaxys

fragmentation pattern; chemical ionization (CI)

Burnier, R. C.; Byrd, G. D.; Freiser, B. S.; Analytical Chemistry; vol. 52; nb. 11; (1980); p. 1641 - 1650, View in Reaxys Thomas; Seyfried; Analytical Chemistry; vol. 21; (1949); p. 1023, View in Reaxys; A.P.I.Res.Project 44 Nr.303<1949>,649<1951>, View in Reaxys; Occolowitz; Journal of the American Chemical Society; vol. 91; (1969); p. 5202, View in Reaxys; Tsuchiya; Adachi; International Journal of Mass Spectrometry and Ion Physics; vol. 20; (1976); p. 7,13, View in Reaxys; Hruza et al.; Journal of Agricultural and Food Chemistry; vol. 22; (1974); p. 123,124, View in Reaxys; Olmsted et al.; Journal of Chemical Physics; vol. 40; (1964); p. 2114,2116, View in Reaxys; McAdoo et al.; Journal of the American Chemical Society; vol. 99; (1977); p. 7265, View in Reaxys; Lersen; Schwarz; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1976); p. 1231, View in Reaxys; Aplin et al.; Journal of the American Chemical Society; vol. 87; (1965); p. 3180,3182, View in Reaxys; Smith; Mc Lafferty; Organic Mass Spectrometry; vol. 5; (1971); p. 483, View in Reaxys; Beckey et al.; International Journal of Mass Spectrometry and Ion Physics; vol. 2; (1969); p. 101,116,117, View in Reaxys; Bondarovich et al.; Journal of Agricultural and Food Chemistry; vol. 15; (1967); p. 36,45, View in Reaxys; Ono et al.; Bulletin of the Chemical Society of Japan; vol. 41; (1968); p. 1793, View in Reaxys; Middlemiss; Harrison; Canadian Journal of Chemistry; vol. 57; (1979); p. 2827,2829-2830, View in Reaxys; Beckey; International Journal of Mass Spectrometry and Ion Physics; vol. 1; (1968); p. 93,96, View in Reaxys; McAdoo et al.; Journal of the American Chemical Society; vol. 100; (1978); p. 6639,6641, 6642, View in Reaxys Elektronenstoss

Happ; Stewart; Journal of the American Chemical Society; vol. 74; (1952); p. 4404,4406, View in Reaxys

UV/VIS Spectroscopy (11) 1 of 11

Description (UV/VIS Spectroscopy)

Vacuum-UV spectrum; Spectrum

Comment (UV/VIS Spectroscopy)

neat (no solvent, gas phase)

Absorption Maxima (UV/ 207.333; 171.511; 159.405; 149.2 VIS) [nm] Vicente; Antunes; Almeida; Franco; Hoffmann; Mason; Eden; Duflot; Canneaux; Delwiche; Hubin-Franskin; Limao-Vieira; Physical Chemistry Chemical Physics; vol. 11; nb. 27; (2009); p. 5729 - 5741, View in Reaxys

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2 of 11

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

1,4-dioxane; tetrachloromethane

Arivazhagan; Parthipan; Thenappan; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 74; nb. 4; (2009); p. 860 - 868, View in Reaxys 3 of 11

Description (UV/VIS Spectroscopy)

UV/VIS

BERG; GUESS; AUTIAN; Journal of pharmaceutical sciences; vol. 54; (1965); p. 79 - 84, View in Reaxys; Caswell et al.; Journal of Organic Chemistry; vol. 41; (1976); p. 3312,3313, View in Reaxys 4 of 11

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

heptane

Platt; Rusoff; Klevens; Journal of Chemical Physics; vol. 11; (1943); p. 541, View in Reaxys 5 of 11

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

Dampf.

Barchewitz; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 208; (1939); p. 808, View in Reaxys 6 of 11

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Ramart-Lucas; Biquard; Grunfeld; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 190; (1930); p. 1197; Annales de Chimie (Cachan, France); vol. <10> 20; (1933); p. 315,316, View in Reaxys; Grunfeld; Annales de Chimie (Cachan, France); vol. <10> 20; (1933); p. 304,367, View in Reaxys 7 of 11

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

aq. HCl

Anslow; Foster; Journal of Biological Chemistry; vol. 97; (1932); p. 39, View in Reaxys 8 of 11

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

H2O

Wright; Journal of the Chemical Society; vol. 103; (1913); p. 529; Journal of the Chemical Society; vol. 105; (1914); p. 670, View in Reaxys; Hantzsch; Scharf; Chemische Berichte; vol. 46; (1913); p. 3580, View in Reaxys; Ley; Arends; Zeitschrift fuer Physikalische Chemie, Abteilung B: Chemie der Elementarprozesse, Aufbau der Materie; vol. 17; (1932); p. 208, View in Reaxys 9 of 11

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

Fluessigkeit.

Hartleb; Strahlentherap.; vol. 39; (1931); p. 442; Chem. Zentralbl.; vol. 102; nb. II; (1931); p. 682, View in Reaxys; Ley; Arends; Zeitschrift fuer Physikalische Chemie, Abteilung B: Chemie der Elementarprozesse, Aufbau der Materie; vol. 17; (1932); p. 208, View in Reaxys 10 of 11

Description (UV/VIS Spectroscopy)

Spectrum

Spring; Recueil des Travaux Chimiques des Pays-Bas; vol. 16; (1897); p. 1, View in Reaxys; Bielecki; Henri; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 155; (1912); p. 457,1619; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 156; (1913); p. 551, View in Reaxys; Hantzsch; Scharf; Chemische Berichte; vol. 46; (1913); p. 3580, View in Reaxys; Bielecki; Henri; Chemische Be-

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richte; vol. 45; (1912); p. 2821;46,2597; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 155; (1912); p. 457, View in Reaxys 11 of 11

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

in Loesung.

Bielecki; Henri; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 155; (1912); p. 457,1619; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 156; (1913); p. 551, View in Reaxys; Hantzsch; Scharf; Chemische Berichte; vol. 46; (1913); p. 3580, View in Reaxys; Bielecki; Henri; Chemische Berichte; vol. 45; (1912); p. 2821;46,2597; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 155; (1912); p. 457, View in Reaxys ESR Spectroscopy (4) 1 of 4

Description (ESR Spectroscopy)

Spectrum

Bennett; Gale; Transactions of the Faraday Society; vol. 64; (1968); p. 1174,1179, 1180, View in Reaxys; Mach et al.; Collection of Czechoslovak Chemical Communications; vol. 44; (1979); p. 3632,3634,3635, View in Reaxys 2 of 4

Description (ESR Spectroscopy)

ESR-hyperfine coupling constants

Bennett; Gale; Transactions of the Faraday Society; vol. 64; (1968); p. 1174,1179, 1180, View in Reaxys; Taniguchi et al.; Bulletin of the Chemical Society of Japan; vol. 45; (1972); p. 3380,3381,3382, View in Reaxys 3 of 4

Description (ESR Spectroscopy)

g-factor

Description (ESR Spectroscopy)

Signals

Neta et al.; Journal of Physical Chemistry; vol. 75; (1971); p. 1654,1661, View in Reaxys Raman Spectroscopy (6) Description (Ram- Comment (Raman Spectroscopy) an Spectroscopy) Spectrum

H2O

References Tanaka, Naoki; Kitano, Hiromi; Ise, Norio; Journal of Physical Chemistry; vol. 94; nb. 16; (1990); p. 6290 - 6292, View in Reaxys; Fischer; Eysel; Journal of Molecular Structure; vol. 415; nb. 3; (1997); p. 249 - 257, View in Reaxys

Spectrum

Dadieu; Kohlrausch; Chemische Berichte; vol. 63; (1930); p. 257; Monatshefte fuer Chemie; vol. 55; (1930); p. 61,57<1931>228, View in Reaxys; Kohlrausch; Koeppl; Pongratz; Zeitschrift fuer Physikalische Chemie, Abteilung B: Chemie der Elementarprozesse, Aufbau der Materie; vol. 21; (1933); p. 254, View in Reaxys; Canals; Gastaud; Bulletin de la Societe Chimique de France; vol. <5>4; (1937); p. 2046, View in Reaxys; Batujew; Doklady Akademii Nauk SSSR; vol. 53; (1946); p. 507; Chem.Abstr.; (1947); p. 2995, View in Reaxys; van den Hende; Bulletin des Societes Chimiques Belges; vol. 54; (1945); p. 91,93; Chem.Abstr.; (1944); p. 3908, View in Reaxys; van den Hende; Fonteyne; Natuurw.Tijdschr.; vol. 25; (1943); p. 25; Chem.Abstr.; (1944); p. 3908, View in Reaxys; Hill; Levin; Journal of Chemical Physics; vol. 70; (1979); p. 842, View in Reaxys; Visser; van der Maas; Journal of Raman Spectroscopy; vol. 7; (1978); p. 125,127, View in Reaxys; Simpson; Journal of Physical Chemistry; vol. 79; (1975); p. 1450,1452, View in Reaxys

Raman

Brutan et al.; Sov. Phys. J. (Engl. Transl.); vol. 10; nb. 2; (1967); p. 150,80, View in Reaxys; Zarakhani et al.; Russian Journal of Physical Chemistry; vol. 39; (1965); p. 831; ; p. 1561, View in Reaxys

Raman intensities

Venkateswarlu; Balasubramanian; Proceedings - Indian Academy of Sciences, Section A; vol. 51; (1960); p. 151,152, View in Reaxys

Spectrum

Gemisch mit Dioxan

Batujew; Doklady Akademii Nauk SSSR; vol. 53; (1946); p. 507; Chem.Abstr.; (1947); p. 2995, View in Reaxys

Spectrum

von fluessiger Buttersaeure

Ganesan; Venkateswaran; Indian J.Phys.; vol. 4; p. 216; Chem. Zentralbl.; vol. 100; nb. II; (1929); p. 2646, View in Reaxys; Venkateswaran; Phil.Mag.; vol. <7>7; p. 599; Chem. Zentralbl.; vol. 100; nb. I; (1929); p. 2389, View in Reaxys; Dadieu; Kohlrausch; Monatshefte fuer Chemie; vol. 52; (1929); p. 231,399,405; Sber.Akad.Wien; vol. 138; p. 52,57, View in Reaxys; Dadieu; Kohlrausch; Phys.Z.; vol. 30; p. 384 Tafel VIII; Chem. Zentralbl.; vol. 100; nb. II; (1929); p. 970, View in Reaxys; Kohlrausch; Phot.Korresp.; vol.

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65; p. 162; Chem. Zentralbl.; vol. 100; nb. II; (1929); p. 1508, View in Reaxys; Dadieu; Kohlrausch; Sber.Akad.Wien; vol. 138; p. 52; Chem. Zentralbl.; vol. 100; nb. II; (1929); p. 697, View in Reaxys Luminescence Spectroscopy (3) Description (LuComment (Lumiminescence nescence SpecSpectroscopy) troscopy)

References

Sonoluminescence

Ashokkumar, Muthupandian; Mulvaney, Paul; Grieser, Franz; Journal of the American Chemical Society; vol. 121; nb. 32; (1999); p. 7355 - 7359, View in Reaxys

pH dependence

Luminescence

Kawada et al.; Nippon Kagaku Kaishi; (1977); p. 345,347, View in Reaxys

Luminescence quenching

Gray et al.; Journal of Chemical Physics; vol. 48; (1968); p. 1145,1148, View in Reaxys

Other Spectroscopic Methods (2) Description (Oth- References er Spectroscopic Methods) Electronic state studies

Vicente; Antunes; Almeida; Franco; Hoffmann; Mason; Eden; Duflot; Canneaux; Delwiche; HubinFranskin; Limao-Vieira; Physical Chemistry Chemical Physics; vol. 11; nb. 27; (2009); p. 5729 - 5741, View in Reaxys

Photoelectron spectrum

Watanabe et al.; Bulletin of the Chemical Society of Japan; vol. 46; (1973); p. 1959,1960, 1962, View in Reaxys

Exposure Assessment (4) Exposure Sources presence in air

emissions from lactating and dry (nonlactating) Holstein dairy cows and their wastes in an environmentally controlled chamber at 18 deg C; University of California, Davis, Department of Animal Science Swiss Research Facility

References Shaw, Stephanie L.; Mitloehner, Frank M.; Jackson, Wendi; Depeters, Edward J.; Fadel, James G.; Robinson, Peter H.; Holzinger, Rupert; Goldstein, Allen H.; Environmental Science and Technology; vol. 41; nb. 4; (2007); p. 1310 - 1316, View in Reaxys

formation in drink- organic matter ing water after containing in the ozonation drinking water taken from Mississippi River near Jefferson Parish, LA, USA

presence in produced waters

Witter, Amy E.; Jones, A. Daniel; Environmental Toxicology and Chemistry; vol. 18; nb. 9; (1999); p. 1920 - 1926, View in Reaxys

California oil-processing facility; March-June 1995

distribution in fog- urban influence waters, Strasbourg, France; sampling from 1991 to 1994; samples were collected from the roof of the Botanical Institute of Strasbourg University (height 30 m)

Cherif; Millet; Sanusi; Herckes; Wortham; Environmental Pollution; vol. 103; nb. 2-3; (1998); p. 301 - 308, View in Reaxys

Concentration in the Environment (20) 1 of 20

Media (Concentration in the Environment)

air

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Location

Iowa, United States

Contamination Concentration

24.2 ng/l

Method, Remarks (Concentration in the Environment)

mean conc.; samples collected from the room where pigs were housed and from headspace of stainless steel storage tanks (24 deg C, 100percent RH) containing fresh manure using graphitized carbon sorbent tubes; thermal desorption GC/MS

Trabue, Steven L.; Scoggin, Kenwood D.; Li, Hong; Burns, Robert; Xin, Hongwei; Environmental Science and Technology; vol. 42; nb. 10; (2008); p. 3745 - 3750, View in Reaxys 2 of 20

Media (Concentration in the Environment)

air

Location

Iowa, United States

Contamination Concentration

3.2 ng/l

Method, Remarks (Concentration in the Environment)

mean conc.; samples collected from the headspace of stainless steel storage tanks (24 deg C, 100percent RH) containing aged manure of pigs using graphitized carbon sorbent tubes; thermal desorption GC/MS

Trabue, Steven L.; Scoggin, Kenwood D.; Li, Hong; Burns, Robert; Xin, Hongwei; Environmental Science and Technology; vol. 42; nb. 10; (2008); p. 3745 - 3750, View in Reaxys 3 of 20

Media (Concentration in the Environment)

air

Location

southeastern United States

Contamination Concentration

10.3 - 129.9 ng/l

Method, Remarks (Concentration in the Environment)

mean conc.; samples taken from various areas in a commercial broiler production house during wintertime conditions (0 deg C, 76percent RH) using graphitized carbon sorbent tubes; thermal desorption GC/MS analyzed

Trabue, Steven L.; Scoggin, Kenwood D.; Li, Hong; Burns, Robert; Xin, Hongwei; Environmental Science and Technology; vol. 42; nb. 10; (2008); p. 3745 - 3750, View in Reaxys 4 of 20

Media (Concentration in the Environment)

air

Location

Iowa, United States

Contamination Concentration

28.8 ng/l

Method, Remarks (Concentration in the Environment)

mean conc.; samples taken ca. 1.0 m height from the floor inside a swine finishing confinement room in Iowa State University Swine Nutrition and Management Research Farm using graphitized carbon sorbent tubes; 15 deg C, 60percent RH; thermal desorption GC/MS

Trabue, Steven L.; Scoggin, Kenwood D.; Li, Hong; Burns, Robert; Xin, Hongwei; Environmental Science and Technology; vol. 42; nb. 10; (2008); p. 3745 - 3750, View in Reaxys 5 of 20

Media (Concentration in the Environment)

groundwater

Location

near Tulsa, Osage county, Oklahoma, USA

Contamination Concentration

1.344 mg/l as C

Method, Remarks (Concentration in the Environment)

sampled on April 1, 2003 from well located at Osage-Skiatook Petroleum Environmental Research site (section 13, T22N, R10E); oil production at this site ended ca. 10 years ago; according to modified EPA method 8270C, 1997; GC/MS analysis

Sirivedhin, Tanita; Dallbauman, Liese; Chemosphere; vol. 57; nb. 6; (2004); p. 463 - 469, View in Reaxys 6 of 20

Media (Concentration in the Environment)

produced water

Location

near Tulsa, Osage county, Oklahoma, USA

Contamination Concentration

1.44 mg/l as C

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Method, Remarks (Concentration in the Environment)

sampled on April 1, 2003 from well actively producing oil located at Osage-Skiatook Petroleum Environmental Research site (section 32, T22N, R11E); according to modified EPA method 8270C, 1997; GC/MS analysis

Sirivedhin, Tanita; Dallbauman, Liese; Chemosphere; vol. 57; nb. 6; (2004); p. 463 - 469, View in Reaxys 7 of 20

Media (Concentration in the Environment)

produced water

Location

near Tulsa, Osage county, Oklahoma, USA

Contamination Concentration

1.776 mg/l as C

Method, Remarks (Concentration in the Environment)

Sirivedhin, Tanita; Dallbauman, Liese; Chemosphere; vol. 57; nb. 6; (2004); p. 463 - 469, View in Reaxys 8 of 20

Media (Concentration in the Environment)

produced water

Location

near Tulsa, Osage county, Oklahoma, USA

Contamination Concentration

1.392 mg/l as C

Method, Remarks (Concentration in the Environment)

sampled on April 1, 2003 from well actively producing oil and coalbed methane located at Osage-Skiatook Petroleum Environmental Research site (section 19, T22N, R12E); according to modified EPA method 8270C, 1997; GC/MS analysis

Sirivedhin, Tanita; Dallbauman, Liese; Chemosphere; vol. 57; nb. 6; (2004); p. 463 - 469, View in Reaxys 9 of 20

Media (Concentration in the Environment)

landfill leachates

Location

Korea

Contamination Concentration

824 mg/l

Method, Remarks (Concentration in the Environment)

age of 5-10 years operated since February 1992 (mainly for municipal wastes); extraction; humic and fulvic acid fractions separated; title comp. determ. with various spectroscopic methods (UV, IR, NMR)

Kang, Ki-Hoon; Shin, Hyun Sang; Park, Heekyung; Water research; vol. 36; nb. 16; (2002); p. 4023 - 4032, View in Reaxys 10 of 20

Media (Concentration in the Environment)

landfill leachates

Location

Korea

Contamination Concentration

4001 mg/l

Method, Remarks (Concentration in the Environment)

age of <5 years operated since August 1996 (mainly for municipal wastes); extraction; humic and fulvic acid fractions separated; title comp. determ. with various spectroscopic methods (UV, IR, NMR)

Kang, Ki-Hoon; Shin, Hyun Sang; Park, Heekyung; Water research; vol. 36; nb. 16; (2002); p. 4023 - 4032, View in Reaxys 11 of 20

Media (Concentration in the Environment)

air

Location

Southern California, USA

Contamination Concentration

0.3 - 0.75 ng/l

Background Concentration

0.01 ng/l

Method, Remarks (Concentration in the Environment)

samples collect. during 2-day photochemical smog episode on Sept. 8-9 1993; 4 sites in Los Angeles basin (Long Beach, Central Los Angeles, Azusa, Claremont); background air samples collect. at San Nicolas Island; high-volume dichotomous sampler; GC-MS

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Nolte, Christopher G.; Fraser, Matthew P.; Cass, Glen R.; Environmental Science and Technology; vol. 33; nb. 4; (1999); p. 540 - 545, View in Reaxys 12 of 20

Media (Concentration in the Environment)

water

Location

North Sea, Norway

Contamination Concentration

22 - 46 mg/l

Method, Remarks (Concentration in the Environment)

samples from offshore oil production platforms Oseberg Feltsenter, Oseberg C, Brage and Troll B collected from October 1995 to August 1996, acidified, homogenized, extracted with CH2Cl2, isotachophoresis

Roe Utvik, Toril I.; Chemosphere; vol. 39; nb. 15; (1999); p. 2593 - 2606, View in Reaxys 13 of 20

Media (Concentration in the Environment)

produced water

Location

California oil-processing facility

Contamination Concentration

0.011 - 1.01 mg/l

Method, Remarks (Concentration in the Environment)

7 produced water samples from California oil-processing facility, collected from March 1 to June 16, 1995; GC/MS

Witter, Amy E.; Jones, A. Daniel; Environmental Toxicology and Chemistry; vol. 18; nb. 9; (1999); p. 1920 - 1926, View in Reaxys 14 of 20

Media (Concentration in the Environment)

waste water

Contamination Concentration

0 - 19 mg/l

Method, Remarks (Concentration in the Environment)

ten samples; collected at different sites in dumping area; filtration through 0.45 μm membrane filter; separation by capillary electrophoresis; measuring indirect UV-absorption

Pantsar-Kallio, Mari; Kuitunen, Minna; Manninen, Pentti K. G.; Chemosphere; vol. 35; nb. 7; (1997); p. 1509 1518, View in Reaxys 15 of 20

Media (Concentration in the Environment)

fogwater

Location

Strasbourg, France

Contamination Concentration

90 - 120 μeq litre-1

Method, Remarks (Concentration in the Environment)

average conc.; collected from the roof of the Botanical Institute of Strasbourg University in 1991; two droplet categories: 2-6 μm and 5-8 μm diameter; UV absorption at 214 nm measured; 18 samples

Millet; Sanusi; Wortham; Environmental Pollution; vol. 94; nb. 3; (1996); p. 345 - 354, View in Reaxys 16 of 20

Media (Concentration in the Environment)

groundwater

Contamination Concentration

63 - 118 mg/l

Method, Remarks (Concentration in the Environment)

from Superfund sites A1 and A2; conc. of organic carbon; GC/MS and LC/MS analyses

Betowski, Leon D.; Kendall, Douglas S.; Pace, Christopher M.; Donnelly, Joseph R.; Environmental Science and Technology; vol. 30; nb. 12; (1996); p. 3558 - 3564, View in Reaxys 17 of 20

Media (Concentration in the Environment)

groundwater

Location

Galloway Township, New Jersey, Virginia, USA

Contamination Concentration

2 μg/l

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Method, Remarks (Concentration in the Environment)

in groundwater of a shallow aquifer contaminated with gasoline (from an underground storage tank); water sampled from probe installed at 15.5 ft below land surface; February 1990; GC/MS

Cozzarelli; Herman; Baedecker; Environmental Science and Technology; vol. 29; nb. 2; (1995); p. 458 - 469, View in Reaxys 18 of 20

Media (Concentration in the Environment)

smoke condensate

Contamination Concentration

0 - 0.14 mg/g

Method, Remarks (Concentration in the Environment)

mean emission factor based on mass of fuel consumed from three separate fires; fuels: ponderosa pine sapwood, needles, bark, litter, duff, and humus; fires: smolder, self-sustained smolder, flaming; bench-scale fires; condensed at -45 deg C

McKenzie; Wei Min Hao; Richards; Ward; Environmental Science and Technology; vol. 29; nb. 8; (1995); p. 2047 2054, View in Reaxys 19 of 20

Media (Concentration in the Environment)

water

Location

Denmark

Contamination Concentration

0.13 - 1.71 mmol/l

Method, Remarks (Concentration in the Environment)

anaerobically pretreatment wastewater from fish, potato, and onion industries, and reject water from anaerobic treatment of excess sludge from municipal wastewater; GC-FID; highest value in potatoes wastewater; lowest value in reject water

Eilersen; Henze; Kloft; Water Research; vol. 29; nb. 5; (1995); p. 1259 - 1266, View in Reaxys 20 of 20

Location

household waste headspace, Denmark

Contamination Concentration

0.01 - 1 mg/m3

Method, Remarks (Concentration in the Environment)

biodegradable waste; GC/MS

Wilkins, Ken; Chemosphere; vol. 29; nb. 1; (1994); p. 47 - 54, View in Reaxys Transport and Distribution (8) 1 of 8

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

gas - particle

Results

gas/particle equilibrium partition coefficient (Kip) at 15 deg C: 6.85E-02 m3/g at 75percent relative humidity

Method, Remarks (Transport and Distribution)

ambient particles collected Berlin, Germany using high volume air sampler with silylated Teflon glass fiber filters; Apr. 10-18, 2006; Kip determ. by inverse gas chromatography using washed (water) particle loaded fiber filters as stationary phase

Arp, Hans Peter H.; Schwarzenbach, Rene P.; Goss, Kai-Uwe; Environmental Science and Technology; vol. 42; nb. 15; (2008); p. 5541 - 5547, View in Reaxys 2 of 8

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

gas - particle

Results

gas/particle equilibrium partition coefficients (Kip) at 15 deg C: 3.06E-02, 5.70E-02 and 1.00E-01 m3/g at 50, 70 and 90percent relative humidity (RH) resp.

Method, Remarks (Transport and Distribution)

ambient particles collected from Berlin, Germany using high volume air sampler with silylated Teflon glass fiber filters; Apr. 10-18, 2006; Kip determ. by inverse gas chromatography using particle loaded fiber filters as stationary phase at various RH

Arp, Hans Peter H.; Schwarzenbach, Rene P.; Goss, Kai-Uwe; Environmental Science and Technology; vol. 42; nb. 15; (2008); p. 5541 - 5547, View in Reaxys

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3 of 8

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

gas - particle

Results

gas/particle equilibrium partition coefficients (Kip) at 15 deg C: 2.15E-02, 5.37E-02 and 7.66E-02 m3/g at 50, 70 and 90percent relative humidity (RH) resp.

Method, Remarks (Transport and Distribution)

ambient particles collected from Duebendorf, Switzerland using high volume air sampler with silylated Teflon glass fiber filter; June 15-20, 2006; Kip determ. by inverse gas chromatography using particle loaded filters as stationary phase at various RH

Arp, Hans Peter H.; Schwarzenbach, Rene P.; Goss, Kai-Uwe; Environmental Science and Technology; vol. 42; nb. 15; (2008); p. 5541 - 5547, View in Reaxys 4 of 8

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

gas - particle

Results

gas/particle equilibrium partition coefficients (Kip) at 15 deg C: 1.25E-01 and 1.90E-01 m3/g at 50percent and 70percent relative humidity (RH) resp.

Method, Remarks (Transport and Distribution)

ambient particles collected from Aspvreten, Sweden using high volume air sampler with silylated Teflon glass fiber filter; Mar. 13-Apr. 3, 2006; Kip determ. by inverse gas chromatography with particle loaded filters as stationary phase at various RH

Arp, Hans Peter H.; Schwarzenbach, Rene P.; Goss, Kai-Uwe; Environmental Science and Technology; vol. 42; nb. 15; (2008); p. 5541 - 5547, View in Reaxys 5 of 8

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

gas - particle

Results

gas/particle equilibrium partition coefficients (Kip) at 15 deg C: 5.71E-02, 5.96E-02 and 8.08E-02 m3/g at 50, 70 and 90percent relative humidity (RH) resp.

Method, Remarks (Transport and Distribution)

ambient particles collected from Roost, Untersiggental, Switzerland using high vol. air sampler with silylated Teflon glass fiber filter; Nov. 5-12, 2006; Kip determ. by inverse gas chromatography with particle loaded filter stationary phase at diff. RH

Arp, Hans Peter H.; Schwarzenbach, Rene P.; Goss, Kai-Uwe; Environmental Science and Technology; vol. 42; nb. 15; (2008); p. 5541 - 5547, View in Reaxys 6 of 8

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

air - Leonardite humic acid

Results

Leonardite humic acid/air partition coefficient, KHA,air = 5.31E5 - 9.41E5 l/kgHA; relative humidity affected experimental partition coefficient by up to a factor of 3

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 7 of 8

Type (Transport and Distribution)

sorption

Media (Transport and Distribution)

air - Leonardite humic acid

Results

experimental sorption enthalpy, ΔabsHi = -43.7 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

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8 of 8

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

air - Leonardite humic acid

Results

Leonardite humic acid/air partition coefficient, KHA,air = 1.04E5 - 5.33E5 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 Biodegradation (27) 1 of 27

Type (Biodegradation)

aerobic

Inoculum

Acinetobacter sp. FW

Concentration (Biodegradation)

1 g/l

Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

bacteria isolated from municipal waste contaminated soil (Dhapa, Kolkata, India); incubated (180 rpm) with title comp.; TLC, HPLC-UV and GC-MS (electron ionization energy) analyses; title comp. utilized as sole source of carbon and energy

Chatterjee, Subhankar; Dutta, Tapan K.; Chemosphere; vol. 70; nb. 5; (2008); p. 933 - 941, View in Reaxys 2 of 27

Type (Biodegradation)

anaerobic reductive dechlorination

Inoculum

soil; Northern Italy

Concentration (Biodegradation)

3 mmol/l

Temperature (Biodegradation) [°C]

18 - 22

Method, Remarks (Biodegradation)

microcosm prepared with soil and groundwater from chlorinated solvent-contaminated aquifer; 240-d incubation in dark with growth factors (yeast extract, vitamin B12) and title comp.; pH: 6.5-7.2; GC-FID; cumulative consumption of title comp. (diagram)

Degradation Product (Biodegradation)

acetate; propanoate

Aulenta, Federico; Pera, Antonio; Rossetti, Simona; Petrangeli Papini, Marco; Majone, Mauro; Water Research; vol. 41; nb. 1; (2007); p. 27 - 38, View in Reaxys 3 of 27

Type (Biodegradation)

sealed vial test

Inoculum

sludge

Method, Remarks (Biodegradation)

sludge from expanded granular sludge bed reactor treating oleic acid; in basal medium containing cysteine hydrochloride and NaHCO3 (pH 7.0-7.2); methanogenic activity: 'not detected' and 52 g-1 VSS d-1 for granular and suspended sludge, resp.

Degradation Product (Biodegradation)

methane

Pereira, Maria Alcina; Roest, Kees; Stams, Alfons J.M; Mota, Manuel; Alves, Madalena; Akkermans, Antoon D.L; FEMS Microbiology Ecology; vol. 41; nb. 2; (2002); p. 95 - 103, View in Reaxys 4 of 27

Type (Biodegradation)

anaerobic

Inoculum

digester sludge and anaerobic biomass, non-adapted

Concentration (Biodegradation)

100 mg/l

Degradation Rate (Biodegradation) [%]

< 5 - 100

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Exposure Period (Biode- 0.5 - 10 d gradation) Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

in sealed serum bottles covered in Al foil; under 70 percent N2/30 percent CO2; shaking at 200 rpm; FeCl2 and Na2S added; degradation profiles; degradation inhibited by Et2O, stearic, oleic and linoleic acids; degradation rates: 0.35-119.3 μg/mgVSS/day

Lalman, Jerald; Bagley, David M; Water Research; vol. 36; nb. 13; (2002); p. 3307 - 3313, View in Reaxys 5 of 27

Type (Biodegradation)

anaerobic

Inoculum

anaerobic sludge; Gao Bei Dian, Beijing

Concentration (Biodegradation)

100 mg/l

Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

incub. for 42 d; pH 7.0; biodegradability of title comp. assessed by 2-(p-iodophenyl)-3-(pnitrophenyl)-5-phenyl tetrazolium chloride dehydrogenase activ.; activity index of anaer. microorganism was 1.1517; title comp. consider. as readily biodegradable

Hongwei, Yang; Zhanpeng, Jiang; Shaoqi, Shi; Tang; Ecotoxicology and Environmental Safety; vol. 53; nb. 3; (2002); p. 416 - 421, View in Reaxys 6 of 27

Type (Biodegradation)

anaerobic

Inoculum

mixture of raw and treated cattle manure

Concentration (Biodegradation)

25 mmol/l

Temperature (Biodegradation) [°C]

55 - 65

Method, Remarks (Biodegradation)

31-l thermophilic lab-scale continuously stirred tank reactor; temperature shift from 55 to 65 deg C reduced the Specific Methanogenic Activity from 47.7 to 3.0 μmol CH4/g VS/h and increased amount of volatile fatty acids in effluent; table; plots

Degradation Product (Biodegradation)

methane

Ahring, Birgitte K.; Ibrahim, Ashraf A.; Mladenovska, Zuzana; Water Research; vol. 35; nb. 10; (2001); p. 2446 2452, View in Reaxys 7 of 27

Type (Biodegradation)

anaerobic

Inoculum

methanogenic bacteria contained in the waste

Concentration (Biodegradation)

19 g/l

Degradation Rate (Biodegradation) [%]

Ca. 100 percent

Exposure Period (Biode- 300 d gradation) Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

three-cell pilot plant; title comp. as a component of a municipal waste; almost complete degradation at the first cell until day 300; more rapid degradation on steps 2 and 3; graphic representation

Degradation Product (Biodegradation)

methane

Rodriguez Iglesias; Castrillon Pelaez; Maranon Maison; Sastre Andres; Water Research; vol. 34; nb. 2; (2000); p. 447 - 454, View in Reaxys 8 of 27

Type (Biodegradation)

anaerobic

Inoculum

mesophilic granular sludge

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Degradation Rate (Biodegradation) [%]

99 percent

Exposure Period (Biode- 25 d gradation) Temperature (Biodegradation) [°C]

55 - 70

Method, Remarks (Biodegradation)

batch test; title comp.-fed upflow anaerobic sludge blanket (USAB) reactor; at 6 h HRT (hydraulic retention time) and 6 g COD l-1 d-1; after 45 d operation at 70 deg C tempr. were shifted: 70-55-70 deg C; decreased (<48 h) removal at each shift

Lepistoe, Raghida; Rintala, Jukka; Water Research; vol. 33; nb. 14; (1999); p. 3162 - 3170, View in Reaxys 9 of 27

Type (Biodegradation)

anaerobic

Inoculum

mesophilic granular sludge

Degradation Rate (Biodegradation) [%]

Ca. 68 percent

Exposure Period (Biode- 367 d gradation) Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

batch test; title comp.-fed upflow anaerobic sludge blanket (USAB) reactor; at 2 h HRT (hydraulic retention time), 2.6 g COD l-1 d-1; sludge beds were halved on day 338; removal reduced in <30 percent and gradually increased to 68 percent; recovery took ca. 12 d

Lepistoe, Raghida; Rintala, Jukka; Water Research; vol. 33; nb. 14; (1999); p. 3162 - 3170, View in Reaxys 10 of 27

Type (Biodegradation)

anaerobic

Inoculum

mesophilic granular sludge

Degradation Rate (Biodegradation) [%]

88 - 91 percent

Exposure Period (Biode- 367 d gradation) Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

batch exper.; title comp.-fed upflow anaerobic sludge blanket (USAB) reactor; at 6 h HRT (hydraulic retention time) and 6 g COD l-1 d-1; on days 186-225 run at 20 deg C without fed; then restart at 70 deg C; title comp. removal started after 11-12 d

Lepistoe, Raghida; Rintala, Jukka; Water Research; vol. 33; nb. 14; (1999); p. 3162 - 3170, View in Reaxys 11 of 27

Type (Biodegradation)

anaerobic

Inoculum

mesophilic granular sludge

Degradation Rate (Biodegradation) [%]

78 - 90 percent

Exposure Period (Biode- 367 d gradation) Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

batch exper.; title comp.-fed upflow anaerobic sludge blanket (USAB) reactor; at 6 h HRT (hydraulic retention time) and 6 g COD l-1 d-1; increasing LVR to 12 g COD l-1 d-1 (HRT ca. 3 h) reduced title comp. removal from ca. 90 percent to 78 percent

Lepistoe, Raghida; Rintala, Jukka; Water Research; vol. 33; nb. 14; (1999); p. 3162 - 3170, View in Reaxys 12 of 27

Type (Biodegradation)

anaerobic

Inoculum

mesophilic granular sludge

Concentration (Biodegradation)

15 mg COD/l

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Degradation Rate (Biodegradation) [%]

13 - 91 percent

Exposure Period (Biode- 324 d gradation) Temperature (Biodegradation) [°C]

35 - 80

Method, Remarks (Biodegradation)

batch experiments; title comp.-fed upflow anaerobic sludge blanket (USAB) reactor; at 2-3 h HRT (hydraulic retention time) and 12-20 g COD l-1 d-1; residual title comp., mg COD/l (incubation temp., deg C): <=4 (35), <=4 (55), 7 (70), 13 (80)

Degradation Product (Biodegradation)

methane

Lepistoe, Raghida; Rintala, Jukka; Water Research; vol. 33; nb. 14; (1999); p. 3162 - 3170, View in Reaxys 13 of 27

Type (Biodegradation)

anaerobic

Inoculum

seed sludge

Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

seed sludge from UASB reactor treating winery wastewater; batch test; Standard Methods (APHA, 1992); influence of heavy metals; pH 7.4-7.7

Degradation Product (Biodegradation)

methane

Lin, Chiu-Yue; Chen, Chin-Chao; Water Research; vol. 33; nb. 2; (1999); p. 409 - 416, View in Reaxys 14 of 27

Type (Biodegradation)

anaerobic

Inoculum

methanogenic sludge

Method, Remarks (Biodegradation)

NMR analysis

Comment (Biodegradation)

Further degradation product(s)

Degradation Product (Biodegradation)

[1,2-13C2]acetic acid; [4,5-13C]valerate; 2-methyl-[2,3-13C]-butyrate

Lens; Dijkema; Stams; Biodegradation; vol. 9; nb. 3-4; (1998); p. 179 - 186, View in Reaxys 15 of 27

Type (Biodegradation)

anaerobic

Inoculum

matrix-associated biomass

Method, Remarks (Biodegradation)

sludge samled from the ADM digester; laboratory-scale quarter-packed hybrid reactor; methanogenic activity measurement

Degradation Product (Biodegradation)

methane

Colleran, Emer; Pender, Sean; Philpott, Una; O'Flaherty, Vincent; Leahy, Brian; Biodegradation; vol. 9; nb. 3-4; (1998); p. 233 - 245, View in Reaxys 16 of 27

Type (Biodegradation)

anaerobic

Inoculum

activated sludge

Method, Remarks (Biodegradation)

sludge samled from the ADM digester; laboratory-scale quarter-packed hybrid reactor; methanogenic activity measurement

Degradation Product (Biodegradation)

methane

Colleran, Emer; Pender, Sean; Philpott, Una; O'Flaherty, Vincent; Leahy, Brian; Biodegradation; vol. 9; nb. 3-4; (1998); p. 233 - 245, View in Reaxys 17 of 27

Type (Biodegradation)

anaerobic

Inoculum

methanogenic granular sludge

Concentration (Biodegradation)

20 mmol/l

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Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

sludge from upflow anaerobic sludge blanket reactors treating potato processing wastewater, Aviko, Steenderen, the Netherlands or blended sludge; in presence of 20 mM acetic acid and 20 mM propionic acid; effect of 0.5-5 mM monochlorophenols

Degradation Product (Biodegradation)

methane; acetic acid

Ennik-Maarsen, Karin A.; Louwerse, Annemarie; Roelofsen, Wim; Stams, Alfons J. M.; Water Research; vol. 32; nb. 10; (1998); p. 2977 - 2982, View in Reaxys 18 of 27

Type (Biodegradation)

anaerobic

Inoculum

methanogenic granular sludge

Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

sludge from upflow anaerobic sludge blanket reactors treating potato processing wastewater, Aviko, Steenderen, the Netherlands; stored for 3 months, incubated for 7 h - 7 d; effect of 1-5 mM 2-chlorophenol

Degradation Product (Biodegradation)

methane; acetic acid

Ennik-Maarsen, Karin A.; Louwerse, Annemarie; Roelofsen, Wim; Stams, Alfons J. M.; Water Research; vol. 32; nb. 10; (1998); p. 2977 - 2982, View in Reaxys 19 of 27

Type (Biodegradation)

aerobic

Inoculum

activated sewage sludge

Concentration (Biodegradation)

100 mg/l

Method, Remarks (Biodegradation)

according to MITI and OECD standard test; growth kinetic parameter values measurement: maximum observed relative growth rate of microorganisms, μmax, 4.1 d-1, half-saturation constant, Ks, < 1 mg ThOD/l

Blok; Struys; Ecotoxicology and Environmental Safety; vol. 33; nb. 3; (1996); p. 217 - 227, View in Reaxys 20 of 27

Type (Biodegradation)

anaerobic

Inoculum

activated sludge

Method, Remarks (Biodegradation)

anaerobic-aerobic activated sludge; batch test; title comp. initial amount: 70-100 mg C/g total suspended soil (TSS); solvent: H2O; incubation time: 4 h; title comp. taken up: 58.7 mg C/g TSS

Comment (Biodegradation)

Further degradation product(s)

Degradation Product (Biodegradation)

3-hydroxyhexanoic acid; 3-Hydroxybutyric acid; 3-hydroxyvaleric acid

Wen-Tso Liu; Mino; Nakamura; Matsuo; Water Research; vol. 30; nb. 1; (1996); p. 75 - 82, View in Reaxys 21 of 27

Type (Biodegradation)

anaerobic

Inoculum

biomass

Temperature (Biodegradation) [°C]

35 - 65

Method, Remarks (Biodegradation)

batch exp.; thermophilic granular sludge (from municipal solid waste, fed with a mix. of sucrose and VFA); max. utilization rate (g COD/g VSS/d): 2.5 at 60 deg C for intact TGS-2 granules, ca. 6 at 60 deg C for crushed TGS-2; Km; cont. flow exp.

Degradation Product (Biodegradation)

methane

Van Lier, Jules B.; Sanz Martin, Jose Luis; Lettinga, Gatze; Water Research; vol. 30; nb. 1; (1996); p. 199 - 207, View in Reaxys 22 of 27

Type (Biodegradation)

aerobic

Inoculum

Acinetobacter lwoffi S2

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Concentration (Biodegradation)

1.0 mmol/l

Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

sodium phosphate buffer (0.01 M); cell suspension (ca. 10 mg dry wt); oxygen uptake (nmol O2/min/mg dry wt) as the ability to oxidation of title comp.: EMKARATE DE 155grown cells: 2.07, n-hexadecane-grown cells: 10.66

Amund; Biodegradation; vol. 7; nb. 2; (1996); p. 91 - 95, View in Reaxys 23 of 27

Type (Biodegradation)

aerobic

Inoculum

Candida utilis

Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

yeast reactor; batch reactor and continuous stirred tank reactor; pH 3.5; critical spacetime: 2 h; maximum specific growth rate: 0.5 1/h; growth yield: 1.05-1.93 kg SS/kg TOC; specific loss rate: 0.05 1/h

Elmaleh; Defrance; Ghommidh; Navarro; Water Research; vol. 30; nb. 10; (1996); p. 2526 - 2529, View in Reaxys 24 of 27

Type (Biodegradation)

anaerobic

Inoculum

wastewater sludge in thermophilic aerobic digester

Concentration (Biodegradation)

Ca. 650 mg/l

Degradation Rate (Biodegradation) [%]

0 percent

Exposure Period (Biode- Ca. 50 h gradation) Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

batch exp. in 1 litre Erlenmeyer flasks; thermophilic aerobic digestion (TAD) process; pH 7; samples taken at various times; volatile fatty acid determination by GC-FID

Chu; Mavinic; Ramey; Kelly; Water Research; vol. 30; nb. 8; (1996); p. 1759 - 1770, View in Reaxys 25 of 27

Type (Biodegradation)

microaerobic

Inoculum

wastewater sludge in thermophilic aerobic digester

Concentration (Biodegradation)

Ca. 750 mg/l

Degradation Rate (Biodegradation) [%]

100 percent

Exposure Period (Biode- Ca. 50 h gradation) Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

batch exp. in 1 litre Erlenmeyer flasks; thermophilic aerobic digestion (TAD) process; pH 7; surface aeration; samples taken at various times; volatile fatty acid determination by GC-FID

Degradation Product (Biodegradation)

acetic acid; carbon dioxide

Chu; Mavinic; Ramey; Kelly; Water Research; vol. 30; nb. 8; (1996); p. 1759 - 1770, View in Reaxys 26 of 27

Type (Biodegradation)

anaerobic

Inoculum

enriched methanogenic culture

Concentration (Biodegradation)

Ca. 0.4 - 2.5 g/l

Temperature (Biodegradation) [°C]

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Method, Remarks (Biodegradation)

acetate and glucose pre-grown inocula; kinetic data: Ks (mg/l): 1194, 1100, Vm (mg/l/h): 5.10, 23.76 (acetate and glucose inoculum, resp.)

Aguilar, Abilio; Casas, Carlos; Lema, Juan M.; Water Research; vol. 29; nb. 2; (1995); p. 505 - 509, View in Reaxys 27 of 27

Type (Biodegradation)

anaerobic

Inoculum

methanogenic granular sludge

Concentration (Biodegradation)

Ca. 4 - 5 mmol/l

Temperature (Biodegradation) [°C]

Method, Remarks (Biodegradation)

in upflow anaerobic sludge blanket reactors; before and after 1-18 months storage at 4 or 22 deg C; time-course of degradation; max. degrad. rate (mmol/gVSS-d): 33.5 and 19.0-35.6 before and after 31 d storage, T: 22 deg C (12 and 72 h after re-feed.)

Degradation Product (Biodegradation)

methane

Wu, Wei-Min; Jain, Mahendra K.; Thiele, Juergen H.; Zeikus, J. Gregory; Water Research; vol. 29; nb. 6; (1995); p. 1445 - 1452, View in Reaxys Abiotic Degradation, Photolysis (1) 1 of 1

Type (Abiotic Degradation, Photolysis)

photooxidation

Concentration (Abiotic Ca. 3 - 10 mmol/m3 Degradation, Photolysis) Temperature (Abiotic 30 Degradation, Photolysis) [°C] Method, Remarks (Abio- title comp. injected in TiO2-coated annular plug-flow reactor; various flow rates; ca. 40 tic Degradation, Photol- W/m2; 50 percent rel. humidity; GC-FID; kinetic follows Langmuir-Hinshelwood; oxidation ysis) rate increased with flow rate; degradation increases with inlet conc.; diagrams Biard, Pierre-Francois; Bouzaza, Abdelkrim; Wolbert, Dominique; Environmental Science and Technology; vol. 41; nb. 8; (2007); p. 2908 - 2914, View in Reaxys Oxygen Demand (2) 1 of 2

Type (Oxygen Demand)

COD/ThOD

Related to

Substance

Ratio BOD5/COD

0.97

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 2 of 2

Type (Oxygen Demand)

BOD5

Related to

Substance

Oxygen Demand [mg O2/l]

0 g/g solute

Method, Remarks (Oxygen Demand)

dead-cell biosensor method; from Bacillus subtilis thermally killed cells; at 25 deg C; pH 7.2; 0.31 M phosphate buffer

Qian, Zhenrong; Tan; Water Research; vol. 32; nb. 3; (1998); p. 801 - 807, View in Reaxys Use (733) Laboratory Use and Handling

Use Pattern

Location

References

Pharmaceuticals

Page/Page column 15

Patent; STICHTING DIENST LANDBOUWKUNDING ONDERZOEK; Boutilier, Kimberly; Angenent, Gerrit Cornelis; Soriano Castan, Mercedes; Hui, Li; (32 pag.); US2016/212956; (2016); (A1) English, View in Reaxys

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histone deacetylase inhibitor (HDACi)

Page/Page column 15

Patent; STICHTING DIENST LANDBOUWKUNDING ONDERZOEK; Boutilier, Kimberly; Angenent, Gerrit Cornelis; Soriano Castan, Mercedes; Hui, Li; (32 pag.); US2016/212956; (2016); (A1) English, View in Reaxys

Other use

Page/Page column 41

Patent; Sanofi Pasteur Biologies, LLC; Fang, Aiqi; White, Andrew James; Tummala, Seshu; Wilson, Lee; US9115347; (2015); (B2) English, View in Reaxys

additive

Page/Page column 41

Patent; Sanofi Pasteur Biologies, LLC; Fang, Aiqi; White, Andrew James; Tummala, Seshu; Wilson, Lee; US9115347; (2015); (B2) English, View in Reaxys

method for obtaining one or more Clostridium difficile (C. difficilel) toxins

Page/Page column 41

Patent; Sanofi Pasteur Biologies, LLC; Fang, Aiqi; White, Andrew James; Tummala, Seshu; Wilson, Lee; US9115347; (2015); (B2) English, View in Reaxys

Pharmaceuticals

Page/Page column 6

Patent; AMOREPACIFIC CORPORATION; Hwang, Jeong Ah; Oh, Yu Jin; Kim, Young Kyung; Chung, Jin Oh; Lee, Sang Jun; Shim, Soon Mi; Chung, Jae Hwan; US2015/283251; (2015); (A1) English, View in Reaxys

anti-aging

Page/Page column 6

Patent; AMOREPACIFIC CORPORATION; Hwang, Jeong Ah; Oh, Yu Jin; Kim, Young Kyung; Chung, Jin Oh; Lee, Sang Jun; Shim, Soon Mi; Chung, Jae Hwan; US2015/283251; (2015); (A1) English, View in Reaxys

anti-oxidation

Page/Page column 6

Patent; AMOREPACIFIC CORPORATION; Hwang, Jeong Ah; Oh, Yu Jin; Kim, Young Kyung; Chung, Jin Oh; Lee, Sang Jun; Shim, Soon Mi; Chung, Jae Hwan; US2015/283251; (2015); (A1) English, View in Reaxys

enhancing catePage/Page colchin bioavailability umn 6

Patent; AMOREPACIFIC CORPORATION; Hwang, Jeong Ah; Oh, Yu Jin; Kim, Young Kyung; Chung, Jin Oh; Lee, Sang Jun; Shim, Soon Mi; Chung, Jae Hwan; US2015/283251; (2015); (A1) English, View in Reaxys

in combination with a cyclodextrin and sugar alcohol

Page/Page column 6

Patent; AMOREPACIFIC CORPORATION; Hwang, Jeong Ah; Oh, Yu Jin; Kim, Young Kyung; Chung, Jin Oh; Lee, Sang Jun; Shim, Soon Mi; Chung, Jae Hwan; US2015/283251; (2015); (A1) English, View in Reaxys

reducing body Page/Page colweight or body fat umn 6

Patent; AMOREPACIFIC CORPORATION; Hwang, Jeong Ah; Oh, Yu Jin; Kim, Young Kyung; Chung, Jin Oh; Lee, Sang Jun; Shim, Soon Mi; Chung, Jae Hwan; US2015/283251; (2015); (A1) English, View in Reaxys

Agricultural use

Page/Page column 8

Patent; The United States of America, as represented by the Secretary of Agriculture; Teal, Peter EA; Duehl, Adrian J.; Carroll, Mark J.; US8647615; (2014); (B1) English, View in Reaxys

attracting honey bee parasitic mites to an object or area, comprising treating the object or area with a composition containing a honey bee parasitic mites with compound

Page/Page column 8

Patent; The United States of America, as represented by the Secretary of Agriculture; Teal, Peter EA; Duehl, Adrian J.; Carroll, Mark J.; US8647615; (2014); (B1) English, View in Reaxys

Agricultural use

Page/Page column 33; 34; 35; 36; 37

Patent; CONTECH ENTERPRISES INC.; TAKACS, Stephen J.; GRIES, Regine M.; GRIES, Gerhard G.; WO2013/3946; (2013); (A1) English, View in Reaxys

Part of rodenticiPage/Page coldal composition umn 33; 34; 35; which attracts and 36; 37 induces feeding by mice and rats

Patent; CONTECH ENTERPRISES INC.; TAKACS, Stephen J.; GRIES, Regine M.; GRIES, Gerhard G.; WO2013/3946; (2013); (A1) English, View in Reaxys

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mosquito repellent

Page/Page column title page; 4

Patent; ZHEJIANG FORESTRY COLLEGE; US2012/45525; (2012); (A1) English, View in Reaxys

component of a mixture for attracting mosquitoes of the genus Anopheles gambiae

Page/Page column title page; 26-28

Patent; WAGENINGEN UNIVERSITEIT; IFAKARA HEALTH INSTITUTE; VAN LOON, Joop, J.A.; WO2010/101462; (2010); (A2) English, View in Reaxys

An elasmobranch repellent

Page/Page column 26

Patent; SHARK DEFENSE L.L.C.; US2010/16346; (2010); (A1) English, View in Reaxys

autism model

MacFabe, Derrick F.; Thomas, Raymond H.; Foley, Kelly A.; Mepham, Jennifer R.; Tichenoff, Lisa J.; Possmayer, Fred; Journal of Neurochemistry; vol. 113; nb. 2; (2010); p. 515 - 529, View in Reaxys

desalting agent for preparation of montelukast form its salt

Patent; DR. REDDY'S LABORATORIES LTD.; DR. REDDY'S LABORATORIES, INC.; WO2009/117381; (2009); (A2) English, View in Reaxys

Solvent for replacement of tissue fluid in cut flowers

Patent; SUNTORY FLOWERS LIMITED; US2009/119801; (2009); (A1) English, View in Reaxys

naso-mucosal; oro-mucosal; respiratory irritants; tissue irritants