Reaxys
PubChem
eMolecules
Reactions (681)
Substances (1)
Citations (829)
Structure
Structure/Compound Data Chemical Name: ethyl 2-hydroxypropionate Reaxys Registry Number: 1209448
CAS Registry Number: 97-64-3, 2676-33-7 Type of Substance: acyclic Molecular Formula: C5H10O3
Linear Structure Formula: HOCH(CH3)C(OC2H5)O Molecular Weight: 118.133 InChI Key: LZCLXQDLBQLTDK-UHFFFAOYSA-N
1
N° of preparations All Preps | All Reactions 91 prep out of 681 reactions.
Available Data
N° of ref.
Identification Physical Data (183) Spectra (39) Bioactivity (63) Other Data (282)
829
Synthesize | Hide Details Find similar Chemical Names and Synonyms ethyl 2-hydroxypropionate, Ethyl lactate, ETHYL LACTATE Identification Substance Label (33) Label
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Patent-Specific Data (9) Prophetic Compound
Related Markush Structure (RN)
Location in Patent
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Related Structure (1) Reference
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Derivative (3) Comment (Derivative)
Reference
Hexafluoroacetonaddukt: 19F-NMR
Leader
Analytical Chemistry, 1973 , vol. 45, p. 1700,1706 Full Text Show Details
Na-salt: Rk. m. phenyliodoso acetate, k, activation parameter (E(A), ΔH(excit.), ΔS(excit.)
Vaidyanathan; Venkatasubramanian
Indian Journal of Chemistry, 1973 , vol. 11, p. 1146 Full Text Show Details
as 2-<(2,4,6-triiodo-phenyl)-carbamoyloxy>-propionic acid ethyl ester (mp: 154 degree )
Johnson
Journal of the Chemical Society, 1955 , p. 3322 Full Text View citing articles Show Details
Physical Data Melting Point (1) Melting Point
Reference
-26 °C
Kennedy, Michael T.
Patent: US2008/75777 A1, 2008 ; Title/Abstract Full Text Show Details
Boiling Point (22) Boiling Point
Pressure (Boiling Point)
Comment (Boiling Point)
Reference
154 °C
Lapkin, Alexei A.; Peters, Martina; Greiner, Lasse; Chemat, Smain; Leonhard, Kai; Liauw, Marcel A.; Leitner, Walter
Green Chemistry, 2010 , vol. 12, # 2 p. 241 - 251 Title/Abstract Full Text View citing articles Show Details
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154 °C
Whittle, Brian Anthony
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CLEAN EARTH TECHNOLOGIES, LLC
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CLEAN EARTH TECHNOLOGIES, LLC
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151 - 155 °C
Title/Abstract Full Text Show Details
Kennedy, Michael T.
Patent: US2008/75777 A1, 2008 ;
154 °C
Title/Abstract Full Text Show Details
Resa, Jose M.; Goenaga, Jose M.; Sanchez-Ruiz, Ana I.; Iglesias, Miguel
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151.83 °C
154 °C
760 Torr
Lecat
Ann. Soc. scient. Bruxelles, 1929 , vol. 49, p. 18 Full Text Show Details
Katagiri, Toshimasa; Yoda, Chika; Furuhashi, Keizo; Ueki, Katsuyuki; Kubota, Toshio
Chemistry Letters, 1996 , # 2 p. 115 - 116 Title/Abstract Full Text View citing articles Show Details
70 - 74 °C
Prasad, J. Siva; Okuniewicz, Frank J.; Delaney, Edward J.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1991 , # 12 p. 3329 - 3332 Title/Abstract Full Text View citing articles Show Details
55 Torr
153 - 154 °C
Clemmensen; Heitman
American Chemical Journal, 1909 , vol. 42, p. 335 Full Text Show Details
Pocker; Davis
Journal of Organic Chemistry, 1975 , vol. 40, p. 1625,1629 Full Text Show Details
150 - 152 °C
Lopatin et al.
Pharmaceutical Chemistry Journal, 1972 , vol. 6, # 11 p. 724 Khimiko-Farmatsevticheskii Zhurnal, 1972 , vol. 6, # 11 p. 36 Full Text View citing articles Show Details
75 °C
42 Torr
Kabbe,H.-J.
Chemische Berichte, 1969 , vol. 102, p. 1404 - 1409 Full Text View citing articles Show Details
67 - 68 °C
27 Torr
Ito
Nippon Kagaku Zasshi, 1962 , vol. 83, p. 195 Chem.Abstr., 1963 , vol. 58, # 11264 Full Text Show Details
51 - 154 °C
10 - 760 Torr
83 - 84 °C
50 Torr
D'Ianni; Adkins
Journal of the American Chemical Society, 1939 , vol. 61, p. 1675,1676 Full Text Show Details
58 °C
19 Torr
Oeda
Bulletin of the Chemical Society of Japan, 1936 , vol. 11, p. 385,387 Full Text View citing articles Show Details
146.8 °C
621.5 Torr
Krige; Hollow
Transactions of the Faraday Society, 1934 , vol. 30, p. 646,647 Full Text Show Details
51 - 52 °C
10 Torr
Rona; Itelsohn-Schechter
Biochemische Zeitschrift, 1928 , vol. 203, p. 295 Full Text Show Details
153.9 °C
760 Torr
Lecat,M.
Recueil des Travaux Chimiques des Pays-Bas, 1926 , vol. 45, p. 622 Recueil des Travaux Chimiques des Pays-Bas, 1928 , vol. 47, p. 15,16 Full Text View citing articles Show Details
65 °C
20 Torr
Simon; Piaux
Bulletin de la Societe de Chimie Biologique, vol. 6, p. 414 Chem. Zentralbl., 1924 , vol. 95, # II p. 1457 Full Text Show Details
67 °C
23 Torr
Wuyts; Bailleux
Bulletin des Societes Chimiques Belges, 1920 , vol. 29, p. 61,66 Chem. Zentralbl., 1920 , vol. 91, # I p. 817 Full Text Show Details
154.8 °C
760 Torr
Wuyts; Bailleux
Bulletin des Societes Chimiques Belges, 1920 , vol. 29, p. 61,66 Chem. Zentralbl., 1920 , vol. 91, # I p. 817 Full Text Show Details
Diagramm.
Rehberg; Dixon
Journal of the American Chemical Society, 1950 , vol. 72, p. 1918,1919 Full Text Show Details
Boiling Point
Pressure (Boiling Point)
Reference
154.5 °C
760 Torr
Schreiner
Justus Liebigs Annalen der Chemie, 1879 , vol. 197, p. 13 Full Text Show Details
154.1 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.124 Full Text Show Details
Refractive Index (16) Refractive Index
Wavelength (Refractive Index)
Temperature (Refractive Index)
Reference
1.413
589 nm
20 °C
Yoon, Ji Hwan; Lee, In Kyu; Choi, Hye Yoon; Choi, Eun Ji; Yoon, Ju Ho; Shim, Sang Eun; Kim, Il
Green Chemistry, 2011 , vol. 13, # 3 p. 631 - 639 Title/Abstract Full Text View citing articles Show Details
1.41973
589 nm
4.99 °C
Aparicio, Santiago; Halajian, Sevanne; Alcalde, Rafael; Garcia, Begona; Leal, Jose M.
Chemical Physics Letters, 2008 , vol. 454, # 1-3 p. 49 - 55 Title/Abstract Full Text View citing articles Show Details
1.41515
589 nm
14.99 °C
Aparicio, Santiago; Halajian, Sevanne; Alcalde, Rafael; Garcia, Begona; Leal, Jose M.
Chemical Physics Letters, 2008 , vol. 454, # 1-3 p. 49 - 55 Title/Abstract Full Text View citing articles Show Details
1.41046
589 nm
24.99 °C
Aparicio, Santiago; Halajian, Sevanne; Alcalde, Rafael; Garcia, Begona; Leal, Jose M.
Chemical Physics Letters, 2008 , vol. 454, # 1-3 p. 49 - 55 Title/Abstract Full Text View citing articles Show Details
1.40604
589 nm
34.99 °C
Aparicio, Santiago; Halajian, Sevanne; Alcalde, Rafael; Garcia, Begona; Leal, Jose M.
Chemical Physics Letters, 2008 , vol. 454, # 1-3 p. 49 - 55 Title/Abstract Full Text View citing articles Show Details
1.40142
589 nm
44.99 °C
Aparicio, Santiago; Halajian, Sevanne; Alcalde, Rafael; Garcia, Begona; Leal, Jose M.
Chemical Physics Letters, 2008 , vol. 454, # 1-3 p. 49 - 55 Title/Abstract Full Text View citing articles Show Details
1.39654
589 nm
54.99 °C
Aparicio, Santiago; Halajian, Sevanne; Alcalde, Rafael; Garcia, Begona; Leal, Jose M.
Chemical Physics Letters, 2008 , vol. 454, # 1-3 p. 49 - 55 Title/Abstract Full Text View citing articles Show Details
1.39194
589 nm
64.99 °C
Aparicio, Santiago; Halajian, Sevanne; Alcalde, Rafael; Garcia, Begona; Leal, Jose M.
Chemical Physics Letters, 2008 , vol. 454, # 1-3 p. 49 - 55 Title/Abstract Full Text View citing articles Show Details
1.4105
589 nm
25 °C
Resa, Jose M.; Goenaga, Jose M.; Sanchez-Ruiz, Ana I.; Iglesias, Miguel
Journal of Chemical and Engineering Data, 2006 , vol. 51, # 4 p. 1294 - 1299 Title/Abstract Full Text View citing articles Show Details
1.414
589 nm
20 °C
Ito
Nippon Kagaku Zasshi, 1962 , vol. 83, p. 195 Chem.Abstr., 1963 , vol. 58, # 11264 Full Text Show Details
1.4125
589 nm
20 °C
Price; Campbell; Warnke
Organic Syntheses, 1951 , vol. 31, p. 60 Full Text Show Details
1.4132
589 nm
20 °C
Rehberg; Dixon
Journal of the American Chemical Society, 1950 , vol. 72, p. 1918,1919 Full Text Show Details
1.404
589 nm
40 °C
Rehberg; Dixon
Journal of the American Chemical Society, 1950 , vol. 72, p. 1918,1919 Full Text Show Details
1.4121
589 nm
25 °C
Smith; Claborn
Industrial and Engineering Chemistry, 1940 , vol. 32, p. 693 Full Text Show Details
1.4124
589 nm
20 °C
Moll
Koll.Beih., 1939 , vol. 49, p. 6 Full Text Show Details
1.4183
589 nm
18 °C
Burkard; Kahovec
Monatshefte fuer Chemie, 1938 , vol. 71, p. 344 Full Text Show Details
Density (26) Density 1.02358 g·cm-3
Reference Temperature
Measurement Temperature
Comment (Density)
Reference
29.99 °C
Liquid
Vani Latha; Little Flower; Rayapa Reddy; Nageswara Rao; Ratnakar
Journal of Molecular Liquids, 2015 , vol. 209, p. 153 - 160 Title/Abstract Full Text View citing articles Show Details
1.00631 g·cm-3
44.99 °C
Press = 0.1 MPa; Liquid
Anila; Rayapa Reddy; Srinivasa Rao; Sairam; Ramachandran; Rambabu
Thermochimica Acta, 2015 , vol. 620, p. 1 - 9 Title/Abstract Full Text View citing articles Show Details
1.01139 g·cm-3
39.99 °C
Press = 0.1 MPa; Liquid
Anila; Rayapa Reddy; Srinivasa Rao; Sairam; Ramachandran; Rambabu
Thermochimica Acta, 2015 , vol. 620, p. 1 - 9 Title/Abstract Full Text View citing articles Show Details
1.01739 g·cm-3
34.99 °C
Press = 0.1 MPa; Liquid
Anila; Rayapa Reddy; Srinivasa Rao; Sairam; Ramachandran; Rambabu
Thermochimica Acta, 2015 , vol. 620, p. 1 - 9 Title/Abstract Full Text View citing articles Show Details
1.02288 g·cm-3
29.99 °C
Press = 0.1 MPa; Liquid
Anila; Rayapa Reddy; Srinivasa Rao; Sairam; Ramachandran; Rambabu
Thermochimica Acta, 2015 , vol. 620, p. 1 - 9 Title/Abstract Full Text View citing articles Show Details
1.05007 g·cm-3
4.99 °C
Aparicio, Santiago; Halajian, Sevanne; Alcalde, Rafael; Garcia, Begona; Leal, Jose M.
Chemical Physics Letters, 2008 , vol. 454, # 1-3 p. 49 - 55 Title/Abstract Full Text View citing articles Show Details
1.03927 g·cm-3
14.99 °C
Aparicio, Santiago; Halajian, Sevanne; Alcalde, Rafael; Garcia, Begona; Leal, Jose M.
Chemical Physics Letters, 2008 , vol. 454, # 1-3 p. 49 - 55 Title/Abstract Full Text View citing articles Show Details
1.02838 g·cm-3
24.99 °C
Aparicio, Santiago; Halajian, Sevanne; Alcalde, Rafael; Garcia, Begona; Leal, Jose M.
Chemical Physics Letters, 2008 , vol. 454, # 1-3 p. 49 - 55 Title/Abstract Full Text View citing articles Show Details
1.01742 g·cm-3
34.99 °C
Aparicio, Santiago; Halajian, Sevanne; Alcalde, Rafael; Garcia, Begona; Leal, Jose M.
Chemical Physics Letters, 2008 , vol. 454, # 1-3 p. 49 - 55 Title/Abstract Full Text View citing articles Show Details
1.00637 g·cm-3
44.99 °C
Aparicio, Santiago; Halajian, Sevanne; Alcalde, Rafael; Garcia, Begona; Leal, Jose M.
Chemical Physics Letters, 2008 , vol. 454, # 1-3 p. 49 - 55 Title/Abstract Full Text View citing articles Show Details
0.99523 g·cm-3
54.99 °C
Aparicio, Santiago; Halajian, Sevanne; Alcalde, Rafael; Garcia, Begona; Leal, Jose M.
Chemical Physics Letters, 2008 , vol. 454, # 1-3 p. 49 - 55 Title/Abstract Full Text View citing articles Show Details
0.98396 g·cm-3
64.99 °C
Aparicio, Santiago; Halajian, Sevanne; Alcalde, Rafael; Garcia, Begona; Leal, Jose M.
Chemical Physics Letters, 2008 , vol. 454, # 1-3 p. 49 - 55 Title/Abstract Full Text View citing articles Show Details
1.0075 - 1.0291 g·cm-3
24.99 - 44.99 °C
Chen, Jui-Tang; Chu, Hsiao-Pei
Journal of Chemical and Engineering Data, 2007 , vol. 52, # 2 p. 650 - 654 Title/Abstract Full Text View citing articles Show Details
1.02802 g·cm-3
25 °C
Resa, Jose M.; Goenaga, Jose M.; Sanchez-Ruiz, Ana I.; Iglesias, Miguel
Journal of Chemical and Engineering Data, 2006 , vol. 51, # 4 p. 1294 - 1299 Title/Abstract Full Text View citing articles Show Details
Lopatin et al.
Pharmaceutical Chemistry Journal, 1972 , vol. 6, # 11 p. 724 Khimiko-Farmatsevticheskii Zhurnal, 1972 , vol. 6, # 11 p. 36 Full Text View citing articles Show Details
1.031 g·cm-3
1.0302 g·cm-3
4 °C
20 °C
Price; Campbell; Warnke
Organic Syntheses, 1951 , vol. 31, p. 60 Full Text Show Details
1.0348 g·cm-3
4 °C
20 °C
Rehberg; Dixon
Journal of the American Chemical Society, 1950 , vol. 72, p. 1918,1919 Full Text Show Details
1.0121 g·cm-3
4 °C
40 °C
Rehberg; Dixon
Journal of the American Chemical Society, 1950 , vol. 72, p. 1918,1919 Full Text Show Details
1.0545 g·cm-3
0 °C
0 °C
Wuyts; Bailleux
Bulletin des Societes Chimiques Belges, 1920 , vol. 29, p. 61,66 Chem. Zentralbl., 1920 , vol. 91, # I p. 817 Full Text Show Details
0.9808 g·cm-3
4 °C
Walden; Swinne
Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre, 1912 , vol. 79, p. 743 Full Text Show Details
70 °C
Density
Reference Temperature
Measurement Temperature
Reference
1.0031 g·cm-3
4 °C
50 °C
Walden; Swinne
Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre, 1912 , vol. 79, p. 743 Full Text Show Details
1.0299 g·cm-3
4 °C
25 °C
Walden; Swinne
Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre, 1912 , vol. 79, p. 743 Full Text Show Details
0.9531 g·cm-3
91 °C
Schreiner
Justus Liebigs Annalen der Chemie, 1879 , vol. 197, p. 13 Full Text Show Details
0.9854 g·cm-3
60 °C
Schreiner
Justus Liebigs Annalen der Chemie, 1879 , vol. 197, p. 13 Full Text Show Details
1.0308 g·cm-3
19 °C
Schreiner
Justus Liebigs Annalen der Chemie, 1879 , vol. 197, p. 13 Full Text Show Details
1.0546 g·cm-3
0 °C
Schreiner
Justus Liebigs Annalen der Chemie, 1879 , vol. 197, p. 13 Full Text Show Details
Azeotropes (MCS) (44) Azeotropes
Temperature (Azeotropes (MCS))
Pressure (Azeotropes (MCS))
Reference
pseudocumene
152.4 °C
760 Torr
Lecat
Ann. Soc. scient. Bruxelles, 1929 , vol. 49, p. 18,20 Full Text Show Details
n-hexyl alcohol
153.6 °C
760 Torr
Lecat
Ann. Soc. scient. Bruxelles, 1929 , vol. 49, p. 18,20 Full Text Show Details
m-xylene
137 °C
760 Torr
Lecat
Recueil des Travaux Chimiques des Pays-Bas, 1927 , vol. 46, p. 243 Ann.Soc.scient.Bruxelles, 1927 , vol. 47 I, p. 112,151,155 Full Text Show Details
mesitylene
150.1 °C
760 Torr
Lecat
Ann. Soc. scient. Bruxelles, 1927 , vol. 47 I, p. 25 Full Text Show Details
propyl isovalerate
150 °C
760 Torr
Lecat
Ann. Soc. scient. Bruxelles, 1927 , vol. 47 I, p. 112 Full Text Show Details
trichlorohydrin
153.7 °C
760 Torr
Lecat,M.
Recueil des Travaux Chimiques des Pays-Bas, 1926 , vol. 45, p. 622 Recueil des Travaux Chimiques des Pays-Bas, 1928 , vol. 47, p. 15,16 Full Text View citing articles Show Details
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.125 Full Text Show Details
camphene
145 °C
760 Torr
Lecat
Ann. Soc. scient. Bruxelles, 1926 , vol. 45 I, p. 174,175 Full Text Show Details
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.127 Full Text Show Details
α-pinene
143.1 °C
760 Torr
Lecat
Ann. Soc. scient. Bruxelles, 1926 , vol. 45 I, p. 174,175
Full Text Show Details
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.126 Full Text Show Details
bromobenzene
149.7 °C
760 Torr
Lecat,M.
Recueil des Travaux Chimiques des Pays-Bas, 1926 , vol. 45, p. 622 Recueil des Travaux Chimiques des Pays-Bas, 1928 , vol. 47, p. 15,16 Full Text View citing articles Show Details
chloroacetal
152.5 °C
760 Torr
Lecat,M.
Recueil des Travaux Chimiques des Pays-Bas, 1926 , vol. 45, p. 622 Recueil des Travaux Chimiques des Pays-Bas, 1928 , vol. 47, p. 15,16 Full Text View citing articles Show Details
cyclohexanol
153.8 °C
760 Torr
Lecat,M.
Recueil des Travaux Chimiques des Pays-Bas, 1926 , vol. 45, p. 622 Recueil des Travaux Chimiques des Pays-Bas, 1928 , vol. 47, p. 15,16 Full Text View citing articles Show Details
cyclohexanone
153.6 °C
760 Torr
Lecat
Ann. Soc. scient. Bruxelles, 1926 , vol. 45 I, p. 174,175 Full Text Show Details
pentachloroethane
153.5 °C
760 Torr
Lecat
Ann. Soc. scient. Bruxelles, 1926 , vol. 45 I, p. 290 Full Text Show Details
1.2.3-trichloro-propane
153.5 °C
760 Torr
Lecat,M.
Recueil des Travaux Chimiques des Pays-Bas, 1926 , vol. 45, p. 622 Recueil des Travaux Chimiques des Pays-Bas, 1928 , vol. 47, p. 15,16 Full Text View citing articles Show Details
pentachloroethane
153.7 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.125 Full Text Show Details
isopentyl iodide
144.5 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.125 Full Text Show Details
2.7-dimethyl-octane
145.5 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.127 Full Text Show Details
α-terpinene
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.127 Full Text Show Details
dipentene
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.127 Full Text Show Details
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.127 Full Text Show Details
β-pinene
147.3 °C
Azeotropes
Temperature (Azeotropes (MCS))
Pressure (Azeotropes (MCS))
Reference
bromobenzene
150.1 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.125 Full Text Show Details
2-chloro-toluene
151 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.125 Full Text Show Details
4-chloro-toluene
152 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.125 Full Text Show Details
o-xylene
140.2 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.126 Full Text Show Details
m-xylene
137.4 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.126 Full Text Show Details
p-xylene
136.6 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.126 Full Text Show Details
propylbenzene
148 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.126 Full Text Show Details
isopropylbenzene
144.5 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.126 Full Text Show Details
pseudocumene
152.3 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.127 Full Text Show Details
mesitylene
150.2 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.127 Full Text Show Details
phenylethylene
140.5 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.126 Full Text Show Details
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.128 Full Text Show Details
dibutyl ether
isopentyl nitrate
146.7 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.124 Full Text Show Details
hexanol-(1)
153.7 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.38 Full Text Show Details
cyclohexanol
154 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.38 Full Text Show Details
anisole
150.1 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.128 Full Text Show Details
ethylene glycol-monopropyl ether
151.3 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.122 Full Text Show Details
chloroacetal
152.8 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.128 Full Text Show Details
cyclohexanone
153.7 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.123 Full Text Show Details
isopentyl propionate
152.8 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.124 Full Text Show Details
isobutyl butyrate
151.5 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.124 Full Text Show Details
isobutyl isobutyrate
146.5 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.124 Full Text Show Details
propyl isovalerate
151 °C
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.124 Full Text Show Details
methylcaproate
760 Torr
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.124 Full Text Show Details
Boundary Surface Phenomena (MCS) (2) Description (Boundary Surface Phenomena (MCS))
Partner (Boundary Surface Phenomena (MCS))
Reference
Surface tension
1-Propyl acetate
Morgan; Griggs
Journal of the American Chemical Society, 1917 , vol. 39, p. 2269 Full Text Show Details
Surface tension
benzene; toluene; propanoic acid methyl ester
Morgan; Griggs
Journal of the American Chemical Society, 1917 , vol. 39, p. 2269 Full Text Show Details
Chromatographic Data (5) Chromatographic data
Original string
Location
Dugo, Giacomo; Franchina, Flavio A.; Scandinaro, Maria R.; Bonaccorsi, Ivana; Cicero, Nicola; Tranchida, Peter Q.; Mondello, Luigi
Food Chemistry, 2014 , vol. 142, p. 262 - 268 Title/Abstract Full Text View citing articles Show Details
Mapitse, Renameditswe; Okatch, Harriet; Moshoeshoe, Eniah
South African Journal of Chemistry, 2014 , vol. 67, p. 184 - 188 Title/Abstract Full Text View citing articles Show Details
Gianotti; Panseri; Robotti; Benzi; Mazzucco; Gosetti; Frascarolo; Oddone; Baldizzone; Marengo; Chiesa
Journal of Chemistry, 2015 , vol. 2015, art. no. 597471 Title/Abstract Full Text View citing articles Show Details
Cao, Gang; Xu, Zhiwei; Wu, Xin; Li, Qingli; Chen, Xiaocheng
Natural Product Research, 2014 , vol. 28, # 19 p. 1607 - 1612 Title/Abstract Full Text Show Details
Onyenekwe, Paul C.; Erhabor, Graham Osas; Akande, Sarah A.
Natural Product Research, 2016 , vol. 30, # 5 p. 558 - 564 Title/Abstract Full Text View citing articles Show Details
Zheng, Yang; Sun, Baoguo; Zhao, Mouming; Zheng, Fuping; Huang, Mingquan; Sun, Jinyuan; Sun, Xiaotao; Li, Hehe
Journal of Agricultural and Food Chemistry, 2016 , vol. 64, # 26 p. 5367 - 5374 Title/Abstract Full Text View citing articles Show Details
GC (Gas chromatography)
UPLC (Ultra performance liquid chromatography)
Reference
4.67 minutes
Paragraph 00056
CARGILL, INCORPORATED; ABRAHAM, Timothy Walter; GOKARN, Ravi R.
Patent: WO2015/58116 A1, 2015 ; Title/Abstract Full Text Show Details
GC (Gas chromatography)
7,1 min
Paragraph 00059
CARGILL, INCORPORATED; ABRAHAM, Timothy Walter; GOKARN, Ravi R.
Patent: WO2015/58116 A1, 2015 ; Title/Abstract Full Text Show Details
GC (Gas chromatography)
6.56 min
Paragraph 00062
CARGILL, INCORPORATED; ABRAHAM, Timothy Walter; GOKARN, Ravi R.
Patent: WO2015/58116 A1, 2015 ; Title/Abstract Full Text Show Details
GC (Gas chromatography)
supporting information
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, 2014 , vol. 28, # 21 p. 1887 - 1893 Title/Abstract Full Text Show Details
Circular Dichroism (2) Location
supporting information
Comment (Circular Dichroism)
Reference
Circular dichroism given
Petrus, Rafal; Bykowski, Dominik; Sobota, Piotr
ACS Catalysis, 2016 , vol. 6, # 8 p. 5222 - 5235 Title/Abstract Full Text View citing articles Show Details
Circular dichroism given
Gu, Zhi-Gang; Buerck, Jochen; Bihlmeier, Angela; Liu, Jinxuan; Shekhah, Osama; Weidler, Peter G.; Azucena, Carlos; Wang, Zhengbang; Heissler, Stefan; Gliemann, Hartmut; Klopper, Wim; Ulrich, Anne S.; Woell, Christof
Chemistry - A European Journal, 2014 , vol. 20, # 32 p. 9879 - 9882 Title/Abstract Full Text View citing articles Show Details
Compressibility (1)
Description (Compressibility)
Comment (Compressibility)
Reference
Adiabatic compressibility
bei 24grad.
Parthasarathy
Current Science, 1937 , vol. 6, p. 213 Chem. Zentralbl., 1938 , vol. 109, # I p. 3164 Full Text Show Details
Crystal Property Description (2) Colour & Other Properties
Location
Reference
yellow
Paragraph 00084
CARGILL, INCORPORATED; ABRAHAM, Timothy Walter; GOKARN, Ravi R.
Patent: WO2015/58116 A1, 2015 ; Title/Abstract Full Text Show Details
Ad Lunam Labs, Inc.
Patent: US2008/153757 A1, 2008 ;
colorless
Title/Abstract Full Text Show Details
Dielectric Constant (1) Reference Crossley; Koizumi
Journal of Chemical Physics, 1974 , vol. 60, p. 4800,4801 Full Text Show Details
Dynamic Viscosity (4) Dynamic Viscosity
Temperature (Dynamic Viscosity)
Reference
0.01494 - 0.02398 P
24.99 - 44.99 °C
Chen, Jui-Tang; Chu, Hsiao-Pei
Journal of Chemical and Engineering Data, 2007 , vol. 52, # 2 p. 650 - 654 Title/Abstract Full Text View citing articles Show Details
0.0261 P
20 °C
Rehberg; Dixon
Journal of the American Chemical Society, 1950 , vol. 72, p. 1918,1919 Full Text Show Details
0.0157 P
40 °C
Rehberg; Dixon
Journal of the American Chemical Society, 1950 , vol. 72, p. 1918,1919 Full Text Show Details
0 - 100 °C
Bingham; Fornwalt
J.Rheol., 1930 , vol. 1, p. 405 Full Text Show Details
Electrical Data (2) Description (Electrical Data)
Reference
Electrical properties
Aparicio, Santiago; Halajian, Sevanne; Alcalde, Rafael; Garcia, Begona; Leal, Jose M.
Chemical Physics Letters, 2008 , vol. 454, # 1-3 p. 49 - 55 Title/Abstract Full Text View citing articles Show Details
Cole-Cole diagram
Lakshminarayana
Journal of Scientific and Industrial Research, Section B: Physical Sciences, 1961 , vol. 20, p. 46,47 Full Text Show Details
Electrical Moment (6) Description (Electrical Moment)
Moment (Electrical Moment)
Temperature (Electrical Moment)
Method (Electrical Moment)
Solvent (Electrical Moment)
Dipole moment
2.5 D
25 °C
Dielectric constant (ε)
cyclohexane
Dipole moment
Comment (Electrical Moment)
Reference Kano, Yoshikazu; Minami, Ryuichi; Takahashi, Hiroaki
Bulletin of the Chemical Society of Japan, 1980 , vol. 53, # 3 p. 642 - 644 Title/Abstract Full Text Show Details
25grad : 2.40 D
Crossley; Koizumi
Journal of Chemical Physics, 1974 ,
vol. 60, p. 4800,4801 Full Text Show Details
Patil; Rao
Current Science, 1973 , vol. 42, p. 68 Full Text Show Details
Dipole moment
Dipole moment
2.14 D
Dielectric constant (ε)
benzene
Narayana
Journal of Scientific and Industrial Research, 1959 , vol. 18B, p. 304 Full Text Show Details
Dipole moment
2.32 D
Dielectric constant (ε)
benzene
Schurz et al.
Monatshefte fuer Chemie, 1955 , vol. 86, p. 986,989 Full Text Show Details
Dipole moment
2.4 D
Dielectric constant (ε)
benzene
Moll
Koll.Beih., 1939 , vol. 49, p. 6 Full Text Show Details
Enthalpy of Combustion (1) Enthalpy of Combustion
Reference
-2.74658E+06 Jmol-1
Luginin
Annales de Chimie (Cachan, France), 1886 , vol. <6> 8, p. 141 Full Text Show Details
Further Information (9) Description (Further Information)
Reference
Further information
Patil; Rao
Current Science, 1973 , vol. 42, p. 68 Full Text Show Details
Further information
Goulden; Manning
Organic Mass Spectrometry, 1970 , vol. 3, p. 1467 Full Text Show Details
Further information
Jaulmes,P.
Bulletin de la Societe Chimique de France, 1969 , p. 3337 - 3349 Full Text View citing articles Show Details
Further information
Welikow et al.
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1967 , p. 1790 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1967 , p. 1862 Full Text Show Details
Further information
Munson; Field
Journal of the American Chemical Society, 1966 , vol. 88, p. 4337,4338 Full Text Show Details
Further information
Bolard
Journal de Chimie Physique et de Physico-Chimie Biologique, 1965 , vol. 62, p. 887,889, 892 Full Text Show Details
Further information
Mori et al.
Bulletin of the Chemical Society of Japan, 1963 , vol. 36, p. 1401 Full Text Show Details
Further information
Lakshminarayana
Journal of Scientific and Industrial Research, Section B: Physical Sciences, 1961 , vol. 20, p. 46,47 Full Text Show Details
Further information
Smith; Coffman
Analytical Chemistry, 1960 , vol. 32, p. 1733,1735 Full Text Show Details
Kinematic Viscosity (1) Kinematic Viscosity
Temperature (Kinematic Viscosity)
Reference
0.0263 St
20 °C
CLEAN EARTH TECHNOLOGIES, LLC
Patent: US2009/62386 A1, 2009 ; Title/Abstract Full Text Show Details
Liquid Phase (2) Description (Liquid Phase)
Comment (Liquid Phase)
Reference
Self-association in solution
in Benzol.
Schurz et al.
Monatshefte fuer Chemie, 1955 , vol. 86, p. 986,989 Full Text Show Details
Trickey
Industrial and Engineering Chemistry, 1927 , vol. 19, p. 643 Chem. Zentralbl., 1927 , vol. 98, # II p. 1396 Full Text View citing articles Show Details
Davidson
Industrial and Engineering Chemistry, 1926 , vol. 18, p. 671 Chem. Zentralbl., 1926 , vol. 97, # II p. 1465 Full Text Show Details
Rate of evaporation
Liquid/Vapour Systems (MCS) (4) Temperature (Liquid/Vapour Systems (MCS))
Description (Liquid/Vapour Systems (MCS))
Partner (Liquid/Vapour Systems (MCS))
Boiling point diagram
ethyl acetate
759.811 Torr
Resa, Jose M.; Goenaga, Jose M.; SanchezRuiz, Ana I.; Iglesias, Miguel
Journal of Chemical and Engineering Data, 2006 , vol. 51, # 4 p. 1294 - 1299 Title/Abstract Full Text View citing articles Show Details
Boiling point diagram
acetic acid methyl ester
759.811 Torr
Resa, Jose M.; Goenaga, Jose M.; SanchezRuiz, Ana I.; Iglesias, Miguel
Journal of Chemical and Engineering Data, 2006 , vol. 51, # 4 p. 1294 - 1299 Title/Abstract Full Text View citing articles Show Details
Liquid/vapour equilibrium
carbon dioxide
37.85 - 49.85 °C
Vapour pressure diagram for the mixture
carbon dioxide
37.85 - 49.85 °C
Pressure (Liquid/Vapour Systems (MCS))
Comment (Liquid/Vapour Systems (MCS))
diagram. Object(s) of Study: equation
Reference
Chylinski, Krzysztof; Gregorowicz, Jacek
Journal of Chemical Thermodynamics, 1998 , vol. 30, # 9 p. 1131 - 1140 Title/Abstract Full Text View citing articles Show Details
Chylinski, Krzysztof; Gregorowicz, Jacek
Journal of Chemical Thermodynamics, 1998 , vol. 30, # 9 p. 1131 - 1140 Title/Abstract Full Text View citing articles Show Details
Magnetic Susceptibility (1) Reference Pascal
Bulletin de la Societe Chimique de France, 1909 , vol. <4>5, p. 1111 Bulletin de la Societe Chimique de France, 1911 , vol. <4>9, p. 181 Full Text Show Details
Mechanical & Physical Properties (MCS) (7) Description (Mechanical & Physical Properties (MCS))
Partner (Mechanical & Physical Properties (MCS))
Temperature (Mechanical & Physical Properties (MCS))
Comment (Mechanical & Physical Properties (MCS))
Volume change on mixing
2-methylpropenoic acid
34.99 °C
diagram
Chen, Jui-Tang; Chu, Hsiao-Pei
Journal of Chemical and Engineering Data, 2007 , vol. 52, # 2 p. 650 - 654 Title/Abstract Full Text View citing articles Show Details
Volume change on mixing
benzyl methacrylate
34.99 °C
diagram
Chen, Jui-Tang; Chu, Hsiao-Pei
Journal of Chemical and Engineering Data, 2007 , vol. 52, # 2 p. 650 - 654 Title/Abstract Full Text View citing articles
Reference
Show Details
Chen, Jui-Tang; Chu, Hsiao-Pei
Journal of Chemical and Engineering Data, 2007 , vol. 52, # 2 p. 650 - 654 Title/Abstract Full Text View citing articles Show Details
Volume change on mixing
ethylene glycol monomethacrylate
34.99 °C
diagram
Ultrasonic velocity
ethyl acetate
25 °C
Resa, Jose M.; Goenaga, Jose M.; SanchezRuiz, Ana I.; Iglesias, Miguel
Journal of Chemical and Engineering Data, 2006 , vol. 51, # 4 p. 1294 - 1299 Title/Abstract Full Text View citing articles Show Details
Volume change on mixing
ethyl acetate
25 °C
Resa, Jose M.; Goenaga, Jose M.; SanchezRuiz, Ana I.; Iglesias, Miguel
Journal of Chemical and Engineering Data, 2006 , vol. 51, # 4 p. 1294 - 1299 Title/Abstract Full Text View citing articles Show Details
Ultrasonic velocity
acetic acid methyl ester
25 °C
Resa, Jose M.; Goenaga, Jose M.; SanchezRuiz, Ana I.; Iglesias, Miguel
Journal of Chemical and Engineering Data, 2006 , vol. 51, # 4 p. 1294 - 1299 Title/Abstract Full Text View citing articles Show Details
Volume change on mixing
acetic acid methyl ester
25 °C
Resa, Jose M.; Goenaga, Jose M.; SanchezRuiz, Ana I.; Iglesias, Miguel
Journal of Chemical and Engineering Data, 2006 , vol. 51, # 4 p. 1294 - 1299 Title/Abstract Full Text View citing articles Show Details
Mechanical Properties (1) Description (Mechanical Properties)
Comment (Mechanical Properties)
Reference
Molar volume
Liquid
Vani Latha; Little Flower; Rayapa Reddy; Nageswara Rao; Ratnakar
Journal of Molecular Liquids, 2015 , vol. 209, p. 153 - 160 Title/Abstract Full Text View citing articles Show Details
Optical Rotatory Power (5) Type (Optical Rotatory Power)
Solvent (Optical Rotatory Power)
Optical Rotatory Power
Wavelength (Optical Rotatory Power)
Temperature (Optical Rotatory Power)
alpha
neat (no solvent)
-10.14 deg
589 nm
25 °C
Seebach, Dieter; Hungerbuehler, Ernst; Naef, Reto; Schnurrenberger, Peter; Weidmann, Beat; Zueger, Max
Synthesis, 1982 , # 2 p. 138 - 141 Title/Abstract Full Text Show Details
[alpha]
11.26 deg
589 nm
18.9 °C
Achiwa
Tetrahedron Letters, 1977 , p. 3735 Full Text View citing articles Show Details
[alpha]
-11.5 deg
589 nm
20 °C
Ragonnet,B. et al.
Helvetica Chimica Acta, 1974 , vol. 57, p. 557 - 566 Full Text View citing articles Show Details
[alpha]
-9.86 deg
589 nm
20 °C
Ragonnet,B. et al.
Helvetica Chimica Acta, 1974 , vol. 57, p. 557 - 566 Full Text View citing articles Show Details
[alpha]
-11 deg
20 °C
Solladie-Cavallo,A.; Vieles,P.
Bulletin de la Societe Chimique de France, 1967 , p. 517 - 523 Full Text View citing articles Show Details
Optics (1) Description (Optics)
Comment (Optics)
Reference
Degree of depolarization of Rayleigh scattering
Depolarisation des Streulichts an fluessigem Aethyllactat.
Bai
Reference
Proceedings - Indian Academy of Sciences, Section A, 1941 , vol. <A> 13, p. 438,446, 448 Proceedings - Indian Academy of Sciences, Section A, 1942 , vol. <A> 15, p. 338,346, 357, 359 Full Text Show Details
Partition octan-1-ol/water (MCS) (1) log POW
Location
Reference
-0.18
Sheet 22
CARGILL, INCORPORATED
Patent: US2010/160623 A1, 2010 ; Title/Abstract Full Text Show Details
Solubility (MCS) (1) Saturation
Comment (Solubility (MCS))
Reference
in pure solvent
pressure dependence. Object(s) of Study: temperature dependence
Chylinski, Krzysztof; Gregorowicz, Jacek
Journal of Chemical Thermodynamics, 1998 , vol. 30, # 9 p. 1131 - 1140 Title/Abstract Full Text View citing articles Show Details
Solution Behaviour (MCS) (3) Description (Solution Behaviour (MCS))
Partner (Solution Behaviour (MCS))
Temperature (Solution Behaviour (MCS))
Pressure (Solution Behaviour (MCS))
Miscibility
methylammonium carbonate
21 - 26 °C
47808 Torr
Dissolving capacity
nitrocellulose
Miscibility
water
Comment (Solution Behaviour (MCS))
Reference Francis
Journal of Physical Chemistry, 1954 , vol. 58, p. 1099,1104 Full Text Show Details
Trickey
Industrial and Engineering Chemistry, 1927 , vol. 19, p. 643 Chem. Zentralbl., 1927 , vol. 98, # II p. 1396 Full Text View citing articles Show Details
in jedem Verhaeltnis.
Lockemann; Ullrich
Desinf., 1925 , vol. 10, p. 104 Full Text Show Details
Sound Properties (2) Description (Sound Properties)
Comment (Sound Properties)
Reference Resa, Jose M.; Goenaga, Jose M.; Sanchez-Ruiz, Ana I.; Iglesias, Miguel
Journal of Chemical and Engineering Data, 2006 , vol. 51, # 4 p. 1294 - 1299 Title/Abstract Full Text View citing articles Show Details
Velocity of sound
in Aethyllactat bei 24grad: 1268 m/sec.
Velocity of sound
Parthasarathy
Current Science, 1937 , vol. 6, p. 213 Chem. Zentralbl., 1938 , vol. 109, # I p. 3164 Full Text Show Details
Static Dielectric Constant (1) Static Dielectric Constant
Temperature (Static Dielectric Constant)
Reference
13.1
20 °C
Moll
Koll.Beih., 1939 , vol. 49, p. 6 Full Text Show Details
Surface Tension (3) Surface Tension
Temperature (Surface Tension)
Reference
29.2 g·s-2
20 °C
Engelhard; Schilfarth; Kaul
Justus Liebigs Annalen der Chemie, 1949 , vol. 563, p. 240 Full Text Show Details
30.3 g·s-2
20 °C
Moll
Koll.Beih., 1939 , vol. 49, p. 6
Full Text Show Details
Morgan; Kramer
Journal of the American Chemical Society, 1913 , vol. 35, p. 1836 Full Text Show Details
Walden; Swinne
Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre, 1912 , vol. 79, p. 743 Full Text Show Details
17.3 - 99.8 °C
20.86 - 28.9 g·s-2
Transport Phenomena (MCS) (3) Description (Transport Phenomena (MCS))
Partner (Transport Phenomena (MCS))
Temperature (Transport Phenomena (MCS))
Dynamic viscosity
2-methylpropenoic acid
24.99 - 44.99 °C
Chen, Jui-Tang; Chu, Hsiao-Pei
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Dynamic viscosity
benzyl methacrylate
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Chen, Jui-Tang; Chu, Hsiao-Pei
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Dynamic viscosity
ethylene glycol monomethacrylate
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Reference
Vapour Pressure (3) Vapour Pressure
Temperature (Vapour Pressure)
Reference
1.65017 Torr
20 °C
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0.79508 Torr
20 °C
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5 Torr
30 °C
Doolittle
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Spectra NMR Spectroscopy (14) Description (NMR Spectroscopy)
Nucleus (NMR Spectroscopy)
Chemical shifts
1H
Coupling Nuclei
Solvents (NMR Spectroscopy)
Frequency (NMR Spectroscopy)
1H NMR (CDCl3): δ 4.3 (q), 4.19 (q), 2.89 (br s), 1.42 (d), 1.33 (t)
chloroform-d1
Spectrum
13C
dimethylsulfoxided6
Chemical shifts
1H
chloroform-d1
Chemical shifts
1H
chloroform-d1
Original Text (NMR Spectroscopy)
Signals
Kind of signal
4.3 ppm 4.19 ppm 2.89 ppm 1.42 ppm 1.33 ppm
q q br s d t
Location Paragraph 0068
Comment (NMR Spectroscopy)
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supporting information
Van Wouwe, Pieter; Dusselier, Michiel; Basic, Aurelie; Sels, Bert F.
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500 MHz
supporting information
Watanabe, Kohtaro; Andou, Yoshito; Shirai, Yosihito; Nishida, Haruo
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Chemical shifts
1H
1H
1H
CDCl3
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CDCl3
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Chemical shifts
1H
CDCl3
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Chemical shifts
13C
CDCl3
75 MHz
Mahindaratne, Mathew P. D.; Wimalasena, Kandatege
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1H
CDCl3
300 MHz
Zhang, Wen; Shi, Min
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CDCl3
300 MHz
Mahindaratne, Mathew P. D.; Wimalasena, Kandatege
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1H
Spin-spin coupling constants
1H
CDCl3
1H-1H
Isayama, Shigeru
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Becker, Hans-Dieter; Ruge, Bernd
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Prasad, J. Siva; Okuniewicz, Frank J.;
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Chemical shifts
13C
Chemical shifts
1H
Bianchi, Giorgio; Achilli, Fiorella; Gamba, Anna; Vercesi, Dina
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benzene-d6
Kamitori, Yasuhiro; Hojo, Masaru; Masuda, Ryoichi; Inoue, Tatsuro; Izumi, Tatsuo
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Bulletin of the Chemical Society of Japan, 1963 , vol. 36, p. 1401 Full Text Show Details
Spectrum
IR Spectroscopy (21) Description (IR Spectroscopy)
Solvent (IR Spectroscopy)
Temperature (IR Spectroscopy)
Comment (IR Spectroscopy)
Reference
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Vani Latha; Little Flower; Rayapa Reddy; Nageswara Rao; Ratnakar
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Bands Spectrum
Anila; Rayapa Reddy; Srinivasa Rao; Sairam; Ramachandran; Rambabu
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ATR (attenuated total reflectance) Intensity of IR bands Bands
24.99 °C
Garca, Gregorio; Aparicio, Santiago; Atilhan, Mert
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Tsui, Hung-Wei; Wang, N.-H. Linda; Franses, Elias I.
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Bands Spectrum
hexane
25 °C
Bands
various solvent(s)
40 °C
pressure dependence. Object(s) of Study: temperature dependence
Grunwaldt, Jan-Dierk; Baiker, Alfons
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Spectrum
various solvent(s)
40 °C
pressure dependence. Object(s) of Study: temperature dependence
Grunwaldt, Jan-Dierk; Baiker, Alfons
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pressure dependence. Object(s) of Study: temperature dependence
Grunwaldt, Jan-Dierk; Baiker, Alfons
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Reflection spectrum
Spectrum
neat liquid
Schneider, Michael S.; Urakawa, Atsushi; Grunwaldt, Jan-Dierk; Buergi, Thomas; Baiker, Alfons
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Bands
neat liquid
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gaseous matrix
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Bands
Borho, Nicole; Suhm, Martin A.
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gaseous matrix
Bands
Bands
neat (no solvent)
Bands
1736 cm**(-1)
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3450 - 1737 cm**(-1)
Isayama, Shigeru
Bulletin of the Chemical Society of Japan, 1990 , vol. 63, # 5 p. 1305 - 1310 Title/Abstract Full Text Show Details
1743 cm**(-1)
Kamitori, Yasuhiro; Hojo, Masaru; Masuda, Ryoichi; Inoue, Tatsuro; Izumi, Tatsuo
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IR
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Mori et al.
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Bolard
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Verbiscar
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Tseng et al.
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Bands
Cohen,S.C.; Khedouri,E.
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Spectrum
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Spectrum
CCl4
3650 - 3430 cm**(-1)
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Spectrum
diethyl ether
3600 - 3325 cm**(-1)
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Temperaturabhaengigkeit.
Freymann
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Spectrum
Description (IR Spectroscopy)
Solvent (IR Spectroscopy)
Reference
Spectrum
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Wulf; Liddel
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CCl4
Mass Spectrometry (2) Description (Mass Spectrometry)
Reference
GCMS (Gas chromatography mass spectrometry) EI (Electron impact) Spectrum
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UV/VIS Spectroscopy (1) Description (UV/VIS Spectroscopy)
Comment (UV/VIS Spectroscopy)
Reference
Spectrum
2350 nm im Ultrarot bis 2.35 micron.
Smith; Boord
Journal of the American Chemical Society, 1926 , vol. 48, p. 1515 Full Text Show Details
Raman Spectroscopy (1) Description (Raman Spectroscopy)
Reference
Spectrum
Bai
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Burkard; Kahovec
Monatshefte fuer Chemie, 1938 , vol. 71, p. 344 Full Text Show Details
Peyches
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Bioactivity Pharmacological Data (63) 1 of 63
Comment (Pharmacological Data)
Bioactivities present
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Bioactivities present
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Bioactivities present
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Bioactivities present
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SASOL GERMANY GMBH
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ALPHARX INC.
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Bioactivities present
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Arkema,
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QLT USA, INC.; WARREN, Stephen, L.; DADEY, Eric; DUNN, Richard, L.; DOWNING, John, Milton; LI, Ellen, Qi
Patent: WO2006/65951 A2, 2006 ; Title/Abstract Full Text Show Details
Lopes, John Alex
Patent: US2006/171978 A1, 2006 ; Title/Abstract Full Text Show Details
ALZA CORPORATION
Patent: WO2006/83799 A2, 2006 ; Title/Abstract Full Text Show Details
ASSISTANCE PUBLIQUE-HOPITAUX DE PARIS; UNIVERSITE PARIS SUD XI
Patent: US2006/210635 A1, 2006 ; Title/Abstract Full Text Show Details
LIVIE BIOPESTICIDES LIMITED; NATIONAL RESEARCH DEVELOPMENT CORPORATION
Patent: WO2006/111692 A1, 2006 ; Title/Abstract Full Text Show Details
PFIZER INC.
Patent: EP230379 B1, 1991 ; Title/Abstract Full Text Show Details
BIODERM RESEARCH
Patent: US2007/31360 A1, 2007 ; Title/Abstract Full Text Show Details
UNIVERSITY OF PITTSBURGH - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION
Patent: WO2007/14237 A2, 2007 ; Title/Abstract Full Text Show Details
Displaytech, Inc.
Patent: US7195719 B1, 2007 ; Title/Abstract Full Text Show Details
Lin, Samuel Qcheng Sun
Patent: US2007/71703 A1, 2007 ; Title/Abstract Full Text Show Details
SYGENTA PARTICIPATIONS AG
Patent: WO2007/73933 A2, 2007 ; Title/Abstract Full Text Show Details
MT2, LLC
Patent: US7314512 B2, 2008 ; Title/Abstract Full Text Show Details
6 of 63
Comment (Pharmacological Data)
Bioactivities present
Reference
Dow AgroSciences LLC
Patent: US2008/58209 A1, 2008 ; Title/Abstract Full Text Show Details
Kennedy, Michael T.
Patent: US2008/75777 A1, 2008 ; Title/Abstract Full Text Show Details
CARDON PHAMACEUTICALS NV
Patent: US2008/103117 A1, 2008 ; Title/Abstract Full Text Show Details
Wurtz; Friedel
Annales de Chimie (Cachan, France), 1861 , vol. <3> 63, p. 108 Full Text View citing articles Show Details
Jungfleisch; Godchot
Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1907 , vol. 144, p. 425 Full Text View citing articles Show Details
Hurd; Filachione
Journal of the American Chemical Society, 1937 , vol. 59, p. 1949,1951 Full Text View citing articles Show Details
Dupire
Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1942 , vol. 214, p. 82 Full Text View citing articles Show Details
Oeda
Bulletin of the Chemical Society of Japan, 1936 , vol. 11, p. 385,387 Full Text View citing articles Show Details
Lecat,M.
Recueil des Travaux Chimiques des Pays-Bas, 1926 , vol. 45, p. 622 Recueil des Travaux Chimiques des Pays-Bas, 1928 , vol. 47, p. 15,16 Full Text View citing articles Show Details
Trickey
Industrial and Engineering Chemistry, 1927 , vol. 19, p. 643 Chem. Zentralbl., 1927 , vol. 98, # II p. 1396 Full Text View citing articles Show Details
Fein; Fisher
Patent: US2448873 , 1945 ; Full Text Show Details
Rehberg; Dixon
Journal of the American Chemical Society, 1950 , vol. 72, p. 5757 Full Text View citing articles Show Details
Rehberg; Dixon
Journal of the American Chemical Society, 1952 , vol. 74, p. 707 Full Text View citing articles Show Details
Fein; Fisher
Journal of the American Chemical Society, 1946 , vol. 68, p. 2631 Full Text View citing articles Show Details
Weygand et al.
Chemische Berichte, 1958 , vol. 91, p. 2534,2536 Full Text View citing articles Show Details
Lacey
Journal of the Chemical Society, 1954 , p. 854,859 Full Text View citing articles Show Details
Haynes; Stanners
Journal of the Chemical Society, 1956 , p. 4103,4105 Full Text View citing articles Show Details
Johnson
Journal of the Chemical Society, 1955 , p. 3322 Full Text View citing articles Show Details
Curtius; Mueller
Chemische Berichte, 1904 , vol. 37, p. 1265 Full Text Show Details
Traube; Ascher
Chemische Berichte, 1913 , vol. 46, p. 2083 Full Text Show Details
7 of 63
Comment (Pharmacological Data)
Bioactivities present
Reference
Bergmann; Miekeley
Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, 1924 , vol. 140, p. 143 Full Text Show Details
Cornforth; Cornforth
Journal of the Chemical Society, 1949 , p. 1028 Full Text Show Details
Shapiro et al.
Journal of the American Chemical Society, 1959 , vol. 81, p. 3993,3994 Full Text Show Details
Davies et al.
Journal of the Chemical Society, 1950 , p. 34 Full Text Show Details
Elmore; Ogle
Tetrahedron, 1958 , vol. 3, p. 310 Full Text View citing articles Show Details
Nachtigall,C.; Ohle,H.
Patent: DE729852 , 1939 ; DRP/DRBP Org.Chem. Full Text Show Details
Chem. Fabr. v. Heyden
Patent: DE729850 , 1941 ; DRP/DRBP Org.Chem. Full Text Show Details
Shapiro et al.
Journal of Organic Chemistry, 1959 , vol. 24, p. 1606 Full Text View citing articles Show Details
Stoughton
Journal of the American Chemical Society, 1941 , vol. 63, p. 2376,2378 Full Text Show Details
Mallinckrodt Chem. Works
Patent: US2338064 , 1940 ; Full Text Show Details
Shapiro et al.
Journal of the American Chemical Society, 1959 , vol. 81, p. 2220,2223 Full Text Show Details
Am. Cyanamid Co.
Patent: US2394526 , 1941 ; Full Text Show Details
Dow Chem. Co.
Patent: US2811535 , 1956 ; Full Text Show Details
Corrodi et al.
Helvetica Chimica Acta, 1957 , vol. 40, p. 2454,2459 Full Text Show Details
Shapiro et al.
Journal of the American Chemical Society, 1958 , vol. 80, p. 6060,6063 Journal of the American Chemical Society, 1959 , vol. 81, p. 203,207 Full Text Show Details
D'Ianni; Adkins
Journal of the American Chemical Society, 1939 , vol. 61, p. 1675,1676 Full Text Show Details
Wright; Gutsell
Journal of the American Chemical Society, 1959 , vol. 81, p. 5193,5197 Full Text Show Details
Brahmachari; Das-Gupta
Journal of the Indian Chemical Society, 1932 , vol. 9, p. 207 Full Text Show Details
Henry
Justus Liebigs Annalen der Chemie, 1870 , vol. 156, p. 176 Full Text Show Details
Findlay; Hickmans
Journal of the Chemical Society, 1909 , vol. 95, p. 1010 Full Text Show Details
8 of 63
Comment (Pharmacological Data)
Bioactivities present
Reference
Schreiner
Justus Liebigs Annalen der Chemie, 1879 , vol. 197, p. 13 Full Text Show Details
Luginin
Annales de Chimie (Cachan, France), 1886 , vol. <6> 8, p. 141 Full Text Show Details
Morgan; Griggs
Journal of the American Chemical Society, 1917 , vol. 39, p. 2269 Full Text Show Details
Ley; Maennchen
Chemische Berichte, 1913 , vol. 46, p. 758 Full Text Show Details
Morgan; Kramer
Journal of the American Chemical Society, 1913 , vol. 35, p. 1836 Full Text Show Details
Dean
Chem. Zentralbl., 1913 , vol. 84, # II p. 347 Full Text Show Details
Berthelot; Gaudechon
Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1911 , vol. 153, p. 385 Full Text Show Details
Walden; Swinne
Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre, 1912 , vol. 79, p. 743 Full Text Show Details
Petrenko-Kritschenko
Chemische Berichte, 1928 , vol. 61, p. 849 Zhurnal Russkago Fiziko-Khimicheskago Obshchestva, 1929 , vol. 61, p. 34 Full Text Show Details
Smith; Boord
Journal of the American Chemical Society, 1926 , vol. 48, p. 1515 Full Text Show Details
Berger
Recueil des Travaux Chimiques des Pays-Bas, 1924 , vol. 43, p. 169,173 Full Text Show Details
Davidson
Industrial and Engineering Chemistry, 1926 , vol. 18, p. 671 Chem. Zentralbl., 1926 , vol. 97, # II p. 1465 Full Text Show Details
Kenyon; Phillips; Turley
Journal of the Chemical Society, 1925 , vol. 127, p. 412 Full Text Show Details
Barker; Skinner
Journal of the American Chemical Society, 1924 , vol. 46, p. 412 Full Text Show Details
Ingold
Journal of the Chemical Society, 1921 , vol. 119, p. 339 Journal of the Chemical Society, 1925 , vol. 127, p. 475 Full Text Show Details
du Pont de Nemours and Co.
Patent: US1882808 , 1928 ; Full Text Show Details
Gerrard
Journal of the Chemical Society, 1940 , p. 228 Full Text Show Details
Fry; Butz
Recueil des Travaux Chimiques des Pays-Bas, 1933 , vol. 52, p. 129 Full Text Show Details
Audrieth; Kleinberg
Journal of Organic Chemistry, 1938 , vol. 3, p. 313 Full Text Show Details
Engelhard; Schilfarth; Kaul
Justus Liebigs Annalen der Chemie, 1949 , vol. 563, p. 240 Full Text Show Details
9 of 63
Comment (Pharmacological Data)
Bioactivities present
Reference
Colon; Warner
Bol.ofic.Asoc.Quim.Puerto RicoChem.Abstr., 1943 , vol. 2, # 2 p. 15 Bol.ofic.Asoc.Quim.Puerto RicoChem.Abstr., 1944 , p. 1165 Full Text Show Details
Salmi
Chemische Berichte, 1939 , vol. 72, p. 1776 Full Text Show Details
Salmi; Leimu
Suomen Kemistilehti B, 1947 , vol. 20, p. 44,46 Chem.Abstr., 1948 , p. 4031 Full Text Show Details
Moll
Koll.Beih., 1939 , vol. 49, p. 6 Full Text Show Details
Doolittle
Industrial and Engineering Chemistry, 1935 , vol. 27, p. 1173 Full Text Show Details
Standard Alcohol Co.
Patent: US2176201 , 1937 ; Full Text Show Details
Cook; McCombie; Saunders
Journal of the Chemical Society, 1945 , p. 874 Full Text Show Details
Gerrard; French
Nature (London, United Kingdom), 1947 , vol. 159, p. 263 Full Text View citing articles Show Details
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.123 Full Text Show Details
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.124 Full Text Show Details
Bai
Proceedings - Indian Academy of Sciences, Section A, 1940 , vol. 11, p. 214,219 Chem.Abstr., 1941 , p. 31 Full Text Show Details
Burkard; Kahovec
Monatshefte fuer Chemie, 1938 , vol. 71, p. 344 Full Text Show Details
Roehm and Haas Co.
Patent: US2091800 , 1931 ; Full Text Show Details
Fourneau; Florence
Bulletin de la Societe Chimique de France, 1930 , vol. <4>47, p. 353 Full Text Show Details
Folkers; Adkins
Journal of the American Chemical Society, 1932 , vol. 54, p. 1146 Full Text Show Details
Comm.Solv.Corp.
Patent: US2029694 , 1934 ; Full Text Show Details
Adkins; Billica
Journal of the American Chemical Society, 1948 , vol. 70, p. 3121 Full Text View citing articles Show Details
Birch; Robinson
Journal of the Chemical Society, 1942 , p. 494 Full Text Show Details
Imp.Chem.Ind.
Patent: US2265814 , 1939 ; Full Text Show Details
Ritchie
Journal of the Chemical Society, 1935 , p. 1061 Full Text Show Details
10 of 63
Comment (Pharmacological Data)
Bioactivities present
Reference
Rehberg; Fisher
Journal of the American Chemical Society, 1945 , vol. 67, p. 57 Full Text Show Details
Rehberg; Dixon; Fisher
Journal of the American Chemical Society, 1945 , vol. 67, p. 209 Full Text Show Details
Adickes; Plessmann; Schmidt
Chemische Berichte, 1937 , vol. 70, p. 2123,2125 Full Text Show Details
Peyches
Bulletin de la Societe Chimique de France, 1935 , vol. <5> 2, p. 2208 Full Text Show Details
Hurd et al.
Journal of the American Chemical Society, 1952 , vol. 74, p. 5128 Full Text View citing articles Show Details
Wolf et al.
Journal of the American Chemical Society, 1956 , vol. 78, p. 4372 Full Text View citing articles Show Details
Bredereck et al.
Chemische Berichte, 1954 , vol. 87, p. 531,534 Chemische Berichte, 1956 , vol. 89, p. 1532 Full Text Show Details
Gerrard et al.
Journal of the Chemical Society, 1958 , p. 3648,3651 Full Text Show Details
Narayana
Journal of Scientific and Industrial Research, 1959 , vol. 18B, p. 304 Full Text Show Details
Minnesota Mining and Mfg.Co.
Patent: US2859240 , 1956 ; Full Text Show Details
Rehberg; Dixon
Journal of the American Chemical Society, 1952 , vol. 74, p. 1095 Full Text View citing articles Show Details
Bruening
Justus Liebigs Annalen der Chemie, 1857 , vol. 104, p. 201 Full Text Show Details
Jones; Neuffer
Journal of the American Chemical Society, 1917 , vol. 39, p. 659 - 668 Full Text Show Details
Eastman Kodak Co.
Patent: US2458420 , 1947 ; Full Text Show Details
Eastman Kodak Co.
Patent: US2458423 , 1947 ; Full Text Show Details
Eastman Kodak Co.
Patent: US2458421 , 1947 ; Full Text Show Details
Eastman Kodak Co.
Patent: US2458422 , 1947 ; Full Text Show Details
Ratchford; Fisher
Journal of Organic Chemistry, 1950 , vol. 15, p. 317,323 Full Text Show Details
Rekker et al.
Recueil des Travaux Chimiques des Pays-Bas, 1951 , vol. 70, p. 113,118 Full Text Show Details
Fein; Filachione
Journal of the American Chemical Society, 1953 , vol. 75, p. 2097 Full Text View citing articles Show Details
11 of 63
Comment (Pharmacological Data)
Bioactivities present
Reference
Shapiro et al.
Journal of the American Chemical Society, 1959 , vol. 81, p. 6322,6323 Full Text Show Details
Shapiro et al.
Journal of the American Chemical Society, 1959 , vol. 81, p. 3083,3084 Full Text Show Details
Sekiya
Yakugaku Zasshi, 1950 , vol. 70, p. 553 Chem.Abstr., 1951 , p. 5619 Full Text Show Details
Cherbuliez; Rabinowitz
Helvetica Chimica Acta, 1956 , vol. 39, p. 1455,1456 Helvetica Chimica Acta, 1958 , vol. 41, p. 1168,1171 Full Text Show Details
Ronwin
Journal of Organic Chemistry, 1953 , vol. 18, p. 127,129 Full Text Show Details
Sprung
Journal of Organic Chemistry, 1958 , vol. 23, p. 1530,1532 Full Text Show Details
Pascal
Bulletin de la Societe Chimique de France, 1909 , vol. <4>5, p. 1111 Bulletin de la Societe Chimique de France, 1911 , vol. <4>9, p. 181 Full Text Show Details
Lecat
Recueil des Travaux Chimiques des Pays-Bas, 1927 , vol. 46, p. 243 Ann.Soc.scient.Bruxelles, 1927 , vol. 47 I, p. 112,151,155 Full Text Show Details
Simon
Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1922 , vol. 175, p. 491 Full Text Show Details
Byk-Guldenwerke A.G.
Patent: DE662732 , 1933 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 25, p. 278 Full Text Show Details
French; Gerrard
Journal of the Chemical Society, 1949 , p. 3329 Full Text Show Details
Gerrard
Journal of the Chemical Society, 1939 , p. 102 Journal of the Chemical Society, 1940 , p. 219,225 Full Text Show Details
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.122 Full Text Show Details
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.128 Full Text Show Details
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.38 Full Text Show Details
Francis
Journal of Physical Chemistry, 1954 , vol. 58, p. 1099,1104 Full Text Show Details
Gerrard; Lappert
Chemistry and Industry (London, United Kingdom), 1952 , p. 53 Full Text Show Details
Gerrard; Woodhead
Journal of the Chemical Society, 1951 , p. 519,521 Full Text Show Details
Gerrard et al.
Research (London), 1955 , vol. 8, p. Spl.7 Full Text Show Details
Green; Hickinbottom
Journal of the Chemical Society, 1957 , p. 3270,3272 Full Text Show Details
12 of 63
Comment (Pharmacological Data)
Bioactivities present
Reference
Pohoryles et al.
Journal of Organic Chemistry, 1959 , vol. 24, p. 1878,1880 Full Text Show Details
Stuckwisch et al.
Journal of Organic Chemistry, 1957 , vol. 22, p. 1678 Full Text View citing articles Show Details
Thiele; Dent
Justus Liebigs Annalen der Chemie, 1898 , vol. 302, p. 262 Full Text Show Details
Traube,W.
Chemische Berichte, 1889 , vol. 22, p. 1577 Full Text Show Details
Clemmensen; Heitman
American Chemical Journal, 1909 , vol. 42, p. 335 Full Text Show Details
Wislicenus
Justus Liebigs Annalen der Chemie, 1863 , vol. 125, p. 62,66 Full Text Show Details
von der Brueggen
Justus Liebigs Annalen der Chemie, 1868 , vol. 148, p. 227 Full Text Show Details
Henry
Chemische Berichte, 1870 , vol. 3, p. 532 Full Text Show Details
Strecker
Justus Liebigs Annalen der Chemie, 1854 , vol. 91, p. 356 Full Text Show Details
Stoermer
Chemische Berichte, 1906 , vol. 39, p. 2302 Full Text Show Details
Aritow; Demjanow
Zhurnal Russkago Fiziko-Khimicheskago Obshchestva, 1887 , vol. 19, p. 262 Chemische Berichte, 20 Ref. <1887>,697 Full Text Show Details
Chem.Fabr.Guestrow
Patent: DE171835 ; Full Text Show Details
Friedel; Wurtz
Annales de Chimie (Cachan, France), 1861 , vol. <3>63, p. 102 Full Text Show Details
Henry
Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften, 1874 , p. 511 Chemische Berichte, 1874 , vol. 7, p. 764 Full Text Show Details
Wislicenus
Justus Liebigs Annalen der Chemie, 1865 , vol. 133, p. 262 Full Text Show Details
Drushel; Dean
Chem. Zentralbl., 1913 , vol. 84, # II p. 135 Full Text Show Details
Chem.Werke Byk
Patent: DE278487 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 12, p. 85 Full Text Show Details
Neuberger
Patent: DE266120 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 11, p. 1181 Full Text Show Details
Curtius
Journal fuer Praktische Chemie (Leipzig), 1917 , vol. <2> 95, p. 211 Full Text Show Details
Rona; Itelsohn-Schechter
Biochemische Zeitschrift, 1928 , vol. 203, p. 295 Full Text Show Details
13 of 63
Comment (Pharmacological Data)
Bioactivities present
Reference
Freudenberg; Rhino
Chemische Berichte, 1924 , vol. 57, p. 1552 Full Text Show Details
C.H. Boehringer Sohn
Patent: DE447838 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 15, p. 382 Full Text Show Details
Lecat
Ann. Soc. scient. Bruxelles, 1927 , vol. 47 I, p. 112 Full Text Show Details
Simon; Piaux
Bulletin de la Societe de Chimie Biologique, vol. 6, p. 414 Chem. Zentralbl., 1924 , vol. 95, # II p. 1457 Full Text Show Details
C.H.Boehringer Sohn
Patent: DE447838 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 15, p. 382 Full Text Show Details
Simon; Piaux
Bulletin de la Societe de Chimie Biologique, vol. 6, p. 415 Chem. Zentralbl., 1924 , vol. 95, # II p. 1457 Full Text Show Details
Lecat
Ann. Soc. scient. Bruxelles, 1926 , vol. 45 I, p. 174,175 Full Text Show Details
Lecat
Ann. Soc. scient. Bruxelles, 1929 , vol. 49, p. 18,20 Full Text Show Details
Lecat
Ann. Soc. scient. Bruxelles, 1927 , vol. 47 I, p. 25 Full Text Show Details
Lecat
Ann. Soc. scient. Bruxelles, 1926 , vol. 45 I, p. 290 Full Text Show Details
Lockemann; Ullrich
Desinf., 1925 , vol. 10, p. 104 Full Text Show Details
Lecat
Ann. Soc. scient. Bruxelles, 1929 , vol. 49, p. 18 Full Text Show Details
Grandiere
Bulletin de la Societe Chimique de France, 1924 , vol. <4> 35, p. 191 Full Text Show Details
Wuyts; Bailleux
Bulletin des Societes Chimiques Belges, 1920 , vol. 29, p. 61,66 Chem. Zentralbl., 1920 , vol. 91, # I p. 817 Full Text Show Details
Fein; Fisher
Industrial and Engineering Chemistry, 1948 , vol. 40, p. 536 Full Text Show Details
Salmi; Leino
Suomen Kemistilehti B, 1944 , vol. 17, p. 20 Chem.Abstr., 1946 , p. 6419 Full Text Show Details
Fisher; Fein
Patent: US2445911 , 1946 ; Full Text Show Details
Rehberg; Fisher
Patent: US2464992 , 1946 ; Full Text Show Details
Ciusa
Atti della Accademia Nazionale dei Lincei, Classe di Scienze Fisiche, Matematiche e Naturali, Rendiconti, 1937 , vol. <6>25, p. 637 Full Text Show Details
Filachione; Fisher
Industrial and Engineering Chemistry, 1944 , vol. 36, p. 473 Full Text Show Details
14 of 63
Comment (Pharmacological Data)
Bioactivities present
Reference
Filachione; Fisher
Patent: US2399595 , 1943 ; Full Text Show Details
Claborn; Smith
Journal of the American Chemical Society, 1939 , vol. 61, p. 2727 Full Text View citing articles Show Details
Glattfeld; Macmillan
Journal of the American Chemical Society, 1936 , vol. 58, p. 899 Full Text Show Details
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.125 Full Text Show Details
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.126 Full Text Show Details
Smith; Claborn
Industrial and Engineering Chemistry, 1940 , vol. 32, p. 693 Full Text Show Details
Higashi
Scientific Papers of the Institute of Physical and Chemical Research (Japan), 1937 , vol. 33, p. 96
Chem. Zentralbl., 1938 , vol. 109, # I p. 1682 Full Text Show Details
Filachione; Lengel; Fisher
Industrial and Engineering Chemistry, 1945 , vol. 37, p. 388,389 Full Text Show Details
Nation.Dairy Research Labor.
Patent: US2434300 , 1945 ; Full Text Show Details
Nation.Dairy Research Labor.
Patent: US2465772 , 1945 ; Full Text Show Details
Sealtest Inc.
Patent: US2390140 , 1944 ; Full Text Show Details
Sealtest Inc.
Patent: US2406648 , 1942 ; Full Text Show Details
Krige; Hollow
Transactions of the Faraday Society, 1934 , vol. 30, p. 646,647 Full Text Show Details
Kulka
Canadian Journal of Research, Section B: Chemical Sciences, 1946 , vol. 24, p. 222 Full Text Show Details
Lecat,M.
Tables azeotropiques, 2.Aufl.<Bruessel 1949>S.127 Full Text Show Details
Freymann
Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1937 , vol. 204, p. 1065 Full Text Show Details
Price; Campbell; Warnke
Organic Syntheses, 1951 , vol. 31, p. 60 Full Text Show Details
Parthasarathy
Current Science, 1937 , vol. 6, p. 213 Chem. Zentralbl., 1938 , vol. 109, # I p. 3164 Full Text Show Details
Bingham; Fornwalt
J.Rheol., 1930 , vol. 1, p. 405 Full Text Show Details
Am.Cyanamid Co.
Patent: US1790262 , 1926 ; Full Text Show Details
15 of 63
Comment (Pharmacological Data)
Bioactivities present
Reference
I.G.Farbenind.
Patent: DE544499 , 1925 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 17, p. 264 Full Text Show Details
Schering-Kahlbaum A.G.
Patent: DE518388 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 17, p. 263,264 Full Text Show Details
Kirchhof; Snajewa
Chim.farm.Promysl., 1933 , p. 280 Chem. Zentralbl., 1934 , vol. 105, # II p. 591 Full Text Show Details
Ciocca; Semproni
Ann.Chim.applic., 1935 , vol. 25, p. 319,320 Chem. Zentralbl., 1935 , vol. 106, # II p. 3084 Full Text Show Details
Gonzalez R.
CienciaChem.Abstr., 1947 , vol. 8, p. 175 CienciaChem.Abstr., 1949 , p. 127 Full Text Show Details
Fein; Fisher
Industrial and Engineering Chemistry, 1944 , vol. 36, p. 236 Industrial and Engineering Chemistry, 1948 , vol. 40, p. 537 Full Text Show Details
Fisher; Fein
Patent: US2374428 , 1943 ; Full Text Show Details
Rehberg; Dixon; Fisher
Journal of Organic Chemistry, 1948 , vol. 13, p. 261 Journal of Organic Chemistry, 1949 , vol. 14, p. 594,600 Full Text Show Details
Kaufmann
Patent: DE641075 , 1931 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 22, p. 545
Full Text Show Details
Kaufmann
Patent: DE528988 , 1928 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 17, p. 2355 Full Text Show Details
du Pont de Nemours and Co.
Patent: US2122716 , 1934 ; Full Text Show Details
Rehberg; Fisher
Patent: US2410551 , 1944 ; Full Text Show Details
Fein; Ratchford; Fisher
Journal of the American Chemical Society, 1944 , vol. 66, p. 1202 Full Text Show Details
Howards and Sons Ltd.
Patent: US2089127 , 1936 ; Full Text Show Details
Howards and Sons Ltd.
Patent: GB456525 ; Full Text Show Details
Kleinberg; Audrieth
Org.Synth.Coll.Vol.III<1955>516 Full Text Show Details
Stoughton
Journal of the American Chemical Society, 1941 , vol. 63, p. 2379 Full Text Show Details
Genevois
Bulletin de la Societe Chimique de France, 1937 , vol. <5> 4, p. 1508 Full Text Show Details
Cornforth
Organic Syntheses, 1951 , vol. 31, p. 59 Full Text Show Details
Byk-Guldenwerke
Patent: DE526366 , 1928 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 17, p. 278 Full Text Show Details
16 of 63
Comment (Pharmacological Data)
Bioactivities present
Reference
Aspelund
Acta Academiae Aboensis, Series B: Mathematica et Physica, 1939 , vol. 11, # 14 p. 3,7 Chem. Zentralbl., 1939 , vol. 110, # II p. 3092 Full Text Show Details
Aspelund
Acta Academiae Aboensis, Series B: Mathematica et Physica, 1937 , vol. 10, # 8 p. 12 Chem. Zentralbl., 1937 , vol. 108, # II p. 1818 Full Text Show Details
Henze; Leslie
Journal of Organic Chemistry, 1950 , vol. 15, p. 901,903 Full Text Show Details
Frazer; Gerrard
Journal of the Chemical Society, 1955 , p. 2959 Full Text Show Details
Schostakowskii et al.
Zhurnal Obshchei Khimii, 1953 , vol. 23, p. 1167,1171;engl.Ausg.S.1227,1229 Full Text Show Details
Troupe; Dimilla
Industrial and Engineering Chemistry, 1957 , vol. 49, p. 847 Full Text Show Details
Fein; Fisher
Patent: US2518456 , 1946 ; Full Text Show Details
Colon et al.
Journal of the American Chemical Society, 1953 , vol. 75, p. 6074 Full Text Show Details
Rehberg; Dixon
Journal of the American Chemical Society, 1950 , vol. 72, p. 1918,1919 Full Text Show Details
Farrington; Sawyer
Journal of the American Chemical Society, 1956 , vol. 78, p. 5536,5539 Full Text Show Details
Kruse et al.
Journal of the American Chemical Society, 1954 , vol. 76, p. 5796 Full Text View citing articles Show Details
Mori et al.
Nippon Kagaku Zasshi, 1956 , vol. 77, p. 459,461,462 Chem.Abstr., 1958 , p. 7858 Full Text Show Details
Eastman Kodak Co.
Patent: US2545044 , 1947 ;
Full Text Show Details
Rehberg; Dixon
Journal of Organic Chemistry, 1950 , vol. 15, p. 973 Full Text View citing articles Show Details
Wendt; Gosting
Journal of Physical Chemistry, 1959 , vol. 63, p. 1287,1289 Full Text Show Details
Stoermer; Riebel
Chemische Berichte, 1906 , vol. 39, p. 2302 Full Text Show Details
Stoermer
Chemische Berichte, 1906 , vol. 39, p. 2304 Full Text Show Details
Vallee
Annales de Chimie (Cachan, France), 1908 , vol. <8> 15, p. 378 Full Text Show Details
Levy
Bulletin de la Societe Chimique de France, 1926 , vol. <4> 39, p. 71 Full Text Show Details
Burns; Jones; Ritchie
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17 of 63
Comment (Pharmacological Data)
Bioactivities present
Reference
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Waters
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Gordon; Miller; Day
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Wulf; Liddel
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Sabetay
Bulletin de la Societe Chimique de France, 1930 , vol. <4> 47, p. 436 Full Text Show Details
Rehberg; Fisher
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Skerrett; Woodcock
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Criegee
Justus Liebigs Annalen der Chemie, 1930 , vol. 481, p. 263,286 Chemische Berichte, 1931 , vol. 64, p. 260,264 Full Text Show Details
C.H. Boehringer Sohn
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Shapiro et al.
Journal of the American Chemical Society, 1959 , vol. 81, p. 5646,5648 Full Text Show Details
Schurz et al.
Monatshefte fuer Chemie, 1955 , vol. 86, p. 986,989 Full Text Show Details
Bai
Proceedings - Indian Academy of Sciences, Section A, 1941 , vol. <A> 13, p. 438,446, 448 Proceedings - Indian Academy of Sciences, Section A, 1942 , vol. <A> 15, p. 338,346, 357, 359 Full Text Show Details
Tiffeneau; Dorlencourt
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Tronow; Kulew
Zhurnal Obshchei Khimii, 1934 , vol. 4, p. 197,200 Chem. Zentralbl., 1935 , vol. 106, # I p. 2794 Full Text Show Details
Hatch; Cram
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Goldenberg,Geromont and Co.
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Goldenberg,Geromont and Co.
Patent: DE70250 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 3, p. 911 Full Text Show Details
Lambling
Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1898 , vol. 127, p. 66 Bulletin de la Societe Chimique de France, 1898 , vol. <3>19, p. 772 Full Text Show Details
Leipen
Monatshefte fuer Chemie, 1888 , vol. 9, p. 48 Full Text Show Details
18 of 63
Comment (Pharmacological Data)
Bioactivities present
Reference
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Glasoe; Audrieth
Journal of Organic Chemistry, 1939 , vol. 4, p. 54,56, 58 Full Text View citing articles Show Details
Shapiro et al.
Journal of the American Chemical Society, 1959 , vol. 81, p. 6498,6503 Full Text Show Details
Kern; Thoma
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Reissert; Kayser
Chemische Berichte, 1889 , vol. 22, p. 2928 Chemische Berichte, 1890 , vol. 23, p. 3702 Full Text Show Details
Reissert; Kayser
Chemische Berichte, vol. 22, p. 2925 Full Text Show Details
Darzens
Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1911 , vol. 152, p. 1603 Full Text Show Details
Santiago; West
Philippine J. Sci., vol. 35, p. 407 Chem. Zentralbl., 1928 , vol. 99, # II p. 1324 Full Text Show Details
Botwinik; Sewerin
Zhurnal Obshchei Khimii, 1950 , vol. 20, p. 1062,1064; engl. Ausg. S. 1101, 1103 Full Text Show Details
Freudenberg; Eichel; Leutert
Chemische Berichte, 1932 , vol. 65, p. 1183,1190 Full Text Show Details
Whitehead
Journal of the American Chemical Society, 1958 , vol. 80, p. 2178,2181 Full Text Show Details
Goldenderg,Geromont and Co.
Patent: DE70250 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 3, p. 911 Full Text Show Details
Schwyzer,J.
Die Fabrikation pharmazeutischer und chemisch-technischer Produkte <Berlin 1931>,S.220 Full Text Show Details
Geigy A.G.
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Heathcock,C.H.; Pirrung,M.C.; Young,S.D.
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Leader
Analytical Chemistry, 1973 , vol. 45, p. 1700,1706 Full Text Show Details
Achiwa
Tetrahedron Letters, 1977 , p. 3735 Full Text View citing articles Show Details
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Pharmaceutical Chemistry Journal, 1972 , vol. 6, # 11 p. 724 Khimiko-Farmatsevticheskii Zhurnal, 1972 , vol. 6, # 11 p. 36 Full Text View citing articles Show Details
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Welti; Stephany
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19 of 63
Comment (Pharmacological Data)
Bioactivities present
Reference
Fenn et al.
Journal of the Chemical Society [Section] B: Physical Organic, 1970 , p. 1044,1046,1047 Full Text View citing articles Show Details
Ito
Agricultural and Biological Chemistry, 1977 , vol. 41, # 7 p. 1307 - 1308 Title/Abstract Full Text View citing articles Show Details
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Journal of the American Chemical Society, 1964 , vol. 86, p. 964 Full Text View citing articles Show Details
Connell
Australian Journal of Chemistry, 1964 , vol. 17, p. 130,131 Full Text Show Details
Mori et al.
Bulletin of the Chemical Society of Japan, 1965 , vol. 38, p. 2199 Full Text Show Details
Munson; Field
Journal of the American Chemical Society, 1966 , vol. 88, p. 4337,4338 Full Text Show Details
Lakshminarayana
Journal of Scientific and Industrial Research, Section B: Physical Sciences, 1961 , vol. 20, p. 46,47 Full Text Show Details
Bamann et al.
Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft, 1960 , vol. 293, p. 175,178 Full Text Show Details
Bolard
Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1963 , vol. 256, p. 4388 Full Text Show Details
Bolard
Journal de Chimie Physique et de Physico-Chimie Biologique, 1965 , vol. 62, p. 887,889, 892 Full Text Show Details
Goulden
Spectrochimica Acta, 1960 , vol. 16, p. 715,716, 717 Full Text View citing articles Show Details
Mori et al.
Bulletin of the Chemical Society of Japan, 1963 , vol. 36, p. 1401 Full Text Show Details
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Bulletin of the Chemical Society of Japan, 1965 , vol. 38, p. 2149,2150 Full Text Show Details
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Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1967 , p. 1790 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1967 , p. 1862 Full Text Show Details
Patil; Rao
Current Science, 1973 , vol. 42, p. 68 Full Text Show Details
Visvanathan
Current Science, 1973 , vol. 42, p. 390 Full Text Show Details
Sundaram; Venkatasubramanian
Indian Journal of Chemistry, 1971 , vol. 9, p. 1102 Full Text Show Details
Venkatasubramanian; Sabesan
Current Science, 1967 , vol. 36, p. 632 Full Text Show Details
Sundaram; Venkatasubramanian
Proceedings - Indian Academy of Sciences, Section A, 1969 , vol. 70, p. 157 Full Text View citing articles Show Details
Swaminathan et al.
Indian Journal of Chemistry, 1975 , vol. 13, p. 1163 Full Text Show Details
20 of 63
Comment (Pharmacological Data)
Bioactivities present
Reference
Goulden; Manning
Organic Mass Spectrometry, 1970 , vol. 3, p. 1467 Full Text Show Details
Vaidyanathan; Venkatasubramanian
Indian Journal of Chemistry, 1973 , vol. 11, p. 1146 Full Text Show Details
Verbiscar
Patent: US3742022 , 1971 ; Chem.Abstr., vol. 79, # 78433 Full Text Show Details
Bhattacharyya et al.
Journal of Applied Chemistry and Biotechnology, 1970 , vol. 20, p. 7 Full Text Show Details
Crossley; Koizumi
Journal of Chemical Physics, 1974 , vol. 60, p. 4800,4801 Full Text Show Details
Ito
Nippon Kagaku Zasshi, 1962 , vol. 83, p. 195 Chem.Abstr., 1963 , vol. 58, # 11264 Full Text Show Details
Mori et al.
Bulletin of the Chemical Society of Japan, 1968 , vol. 41, p. 1871,1873
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Tseng et al.
Tetrahedron Letters, 1971 , p. 3053,3055 Full Text Show Details
Pocker; Davis
Journal of Organic Chemistry, 1975 , vol. 40, p. 1625,1629 Full Text Show Details
Lee; Downie
Tetrahedron, 1967 , vol. 23, p. 359 Full Text View citing articles Show Details
Cave; Galons; Miocque; Rinjard; Tran; Binet
European Journal of Medicinal Chemistry, 1990 , vol. 25, # 1 p. 75 - 79 Title/Abstract Full Text View citing articles Show Details
Isayama, Shigeru
Bulletin of the Chemical Society of Japan, 1990 , vol. 63, # 5 p. 1305 - 1310 Title/Abstract Full Text Show Details
Drewes, Siegfried E.; Emslie, Neville D.; Karodia, Nazira
Synthetic Communications, 1990 , vol. 20, # 13 p. 1915 - 1921 Title/Abstract Full Text Show Details
Yamamoto, Kimiko; Nakao, Yoshihiko; Kyogoku, Yoshimasa; Sugeta, Hiromu
Journal of Molecular Structure, 1991 , vol. 242, # 1 p. 75 - 86 Title/Abstract Full Text View citing articles Show Details
Togo, Hideo; Fujii, Misa; Yokoyama, Masataka
Bulletin of the Chemical Society of Japan, 1991 , vol. 64, # 1 p. 57 - 67 Title/Abstract Full Text Show Details
Kamitori, Yasuhiro; Hojo, Masaru; Masuda, Ryoichi; Inoue, Tatsuro; Izumi, Tatsuo
Tetrahedron Letters, 1982 , vol. 23, # 44 p. 4585 - 4588 Title/Abstract Full Text View citing articles Show Details
Boeckman, Robert K.; Potenza, Joan C.
Tetrahedron Letters, 1985 , vol. 26, # 11 p. 1411 - 1414 Title/Abstract Full Text Show Details
Alvernhe, G.; Laurent, A.; Masrua, A.
Tetrahedron Letters, 1983 , vol. 24, # 11 p. 1153 - 1156 Title/Abstract Full Text View citing articles Show Details
Tsuchihashi, Gen-ichi; Tomooka, Katsuhiko; Suzuki, Keisuke
Tetrahedron Letters, 1984 , vol. 25, # 38 p. 4253 - 4256 Title/Abstract Full Text View citing articles Show Details
Booth, Paul M.; Fox, Christina M. J.; Ley, Steven V.
Tetrahedron Letters, 1983 , vol. 24, # 46 p. 5143 - 5146 Title/Abstract Full Text View citing articles Show Details
21 of 63
Comment (Pharmacological Data)
Bioactivities present
Reference
Walkup, Robert D.
Tetrahedron Letters, 1987 , vol. 28, # 5 p. 511 - 514 Title/Abstract Full Text View citing articles Show Details
Kafka, Stanislav; Cermak, Jan; Novak, Tomas; Pudil, Frantisek; Viden, Ivan; Ferles, Miloslav
Collection of Czechoslovak Chemical Communications, 1985 , vol. 50, # 5 p. 1201 - 1211 Title/Abstract Full Text Show Details
Ferles, Miloslav; Silhankova, Alexandra; Kafka, Stanislav; Taufmann, Petr; Motacek, Tomas
Collection of Czechoslovak Chemical Communications, 1983 , vol. 48, # l p. 1759 - 1764 Title/Abstract Full Text Show Details
Pridgen, Lendon N.; Miller, George
Journal of Heterocyclic Chemistry, 1983 , vol. 20, p. 1223 - 1230 Title/Abstract Full Text Show Details
Morita, Hiroyuki; Shiotani,Shunsaku
Journal of Heterocyclic Chemistry, 1986 , vol. 23, p. 1465 - 1469 Title/Abstract Full Text Show Details
Becker, Hans-Dieter; Ruge, Bernd
Journal of Organic Chemistry, 1980 , vol. 45, # 11 p. 2189 - 2195 Title/Abstract Full Text View citing articles Show Details
Ohta, Shunsaku; Shimabayashi, Akihiro; Hayakawa, Satoshi; Sumino, Motoshige; Okamoto, Masao
Synthesis, 1985 , # 1 p. 45 - 48 Title/Abstract Full Text Show Details
Seebach, Dieter; Hungerbuehler, Ernst; Naef, Reto; Schnurrenberger, Peter; Weidmann, Beat; Zueger, Max
Synthesis, 1982 , # 2 p. 138 - 141 Title/Abstract Full Text Show Details
Namy, J. L.; Souppe, J.; Collin, J.; Kagan, H. B.
Journal of Organic Chemistry, 1984 , vol. 49, # 11 p. 2045 - 2049 Title/Abstract Full Text View citing articles Show Details
Tlegenov, R. T.; Dalimov, D. N.; Khaitbaev, Kh. Kh.; Abduvakhabov, A. A.; Uteniyazov, K. U.
Chemistry of Natural Compounds, 1990 , vol. 26, # 4 p. 434 - 436 Khimiya Prirodnykh Soedinenii, 1990 , # 4 p. 513 - 515 Title/Abstract Full Text View citing articles Show Details
Nishiyama, Tomihiro; Iwasaki, Yoshiaki; Nishikawa, Takeshi; Miyatake, Shinji; Yamada, Fukiko
Journal of Heterocyclic Chemistry, 1991 , vol. 28, # 5 p. 1369 - 1372 Title/Abstract Full Text Show Details
Brunner, H.; Amberger, K.; Wischert, T.; Wiehl, J.
Bulletin des Societes Chimiques Belges, 1991 , vol. 100, # 8 p. 585 - 595 Title/Abstract Full Text Show Details
Yamamoto, Makoto; Dewa, Toshikazu; Munakata, Hiroshi; Kohmoto, Shigeo; Yamada, Kazutoshi
Journal of Chemical Research, Miniprint, 1991 , # 7 p. 1771 - 1782 Title/Abstract Full Text Show Details
Enholm, Eric J.; Jiang, Shujun
Tetrahedron Letters, 1992 , vol. 33, # 3 p. 313 - 316 Title/Abstract Full Text View citing articles Show Details
Booth, Paul M.; Fox, Christina, M. J.; Ley, Steve V.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1987 , p. 121 - 130 Title/Abstract Full Text Show Details
Bianchi, Giorgio; Achilli, Fiorella; Gamba, Anna; Vercesi, Dina
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1988 , p. 417 - 422 Title/Abstract Full Text View citing articles Show Details
Watanabe, Yoshihisha; Ota, Tetsuo; Tsuji, Yasushi
Chemistry Letters, 1980 , p. 1585 - 1586 Title/Abstract Full Text Show Details
Annunziata, Rita; Cinquini, Mauro; Cozzi, Franco; Gilardi, Amilcare; Cardani, Silvia; et al.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1985 , p. 255 - 260 Title/Abstract Full Text Show Details
Stachel, Hans-Dietrich; Hampl, Bernhard
Chemische Berichte, 1981 , vol. 114, # 1 p. 405 - 411 Title/Abstract Full Text Show Details
Heathcock, Clayton H.; Hagen, James P.; Jarvi, Esa T.; Pirrung, Michael C.; Young, Steven D.
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22 of 63
Comment (Pharmacological Data)
Bioactivities present
Reference
Lapkin, I. I.; Kolbina, N. M.; Tatarenko, O. I.
Journal of Organic Chemistry USSR (English Translation), 1987 , vol. 23, # 2 p. 279 - 281 Zhurnal Organicheskoi Khimii, 1987 , vol. 23, # 2 p. 315 - 317 Title/Abstract Full Text Show Details
Wheeler, Thomas N.; Craig, Todd A.; Morland, Robert B.; Ray, John, A.
Synthesis, 1987 , # 10 p. 883 - 887 Title/Abstract Full Text Show Details
Saha, Ashis K.; Schultz, Peter; Rapoport, Henry
Journal of the American Chemical Society, 1989 , vol. 111, # 13 p. 4856 - 4859 Title/Abstract Full Text View citing articles Show Details
Prasad, J. Siva; Okuniewicz, Frank J.; Delaney, Edward J.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1991 , # 12 p. 3329 - 3332 Title/Abstract Full Text View citing articles Show Details
Creary, Xavier; Hatoum, Holia N.; Barton, Angela; Aldridge, Timothy E.
Journal of Organic Chemistry, 1992 , vol. 57, # 6 p. 1887 - 1897 Title/Abstract Full Text View citing articles Show Details
Hatakeyama, Susumi; Sugawara, Makiko; Kawamura, Mitsuhiro; Takano, Seiichi
Journal of the Chemical Society, Chemical Communications, 1992 , # 17 p. 1229 - 1231 Title/Abstract Full Text View citing articles Show Details
Solladie-Cavallo, A.; Bencheqroun, M.
Journal of Organic Chemistry, 1992 , vol. 57, # 22 p. 5831 - 5834 Title/Abstract Full Text View citing articles Show Details
Yamato, Masatoshi; Ishikawa, Tadataka; Kobayashi, Toshio
Chemical and Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 2967 - 2971 Title/Abstract Full Text Show Details
Kano, Shinzo; Yuasa, Yoko; Yokomatsu, Tsutomu; Shibuya, Shiroshi
Chemistry Letters, 1983 , p. 1475 - 1476 Title/Abstract Full Text Show Details
Akiba, Kin-ya; Ohnari, Hideyuki; Ohkata, Katsuo
Chemistry Letters, 1985 , p. 1577 - 1580 Title/Abstract Full Text Show Details
Mukaiyama, Teruaki; Ichikawa, Junji; Asami, Masatoshi
Chemistry Letters, 1983 , p. 293 - 296 Title/Abstract Full Text Show Details
Mishra, J. P.; Bansal, N. L.
Zeitschrift fuer Physikalische Chemie (Leipzig), 1981 , vol. 262, # 4 p. 683 - 690 Title/Abstract Full Text Show Details
Lapkin, I. I.; Kolbina, N. M.; Tatarenko, O. I.; Prokhorova, T. S.; Gartman, G. A.
Pharmaceutical Chemistry Journal, 1987 , vol. 21, # 11 p. 778 - 779 Khimiko-Farmatsevticheskii Zhurnal, 1987 , vol. 21, # 11 p. 1326 - 1328 Title/Abstract Full Text View citing articles Show Details
Yamamoto, Yoshinori; Chounan, Yukiyasu; Nishii, Shinji; Ibuka, Toshiro; Kitahara, Haruo
Journal of the American Chemical Society, 1992 , vol. 114, # 20 p. 7652 - 7660 Title/Abstract Full Text View citing articles Show Details
DesMarteau; Petrov; Montanari; Pregnolato; Resnati
Tetrahedron Letters, 1992 , vol. 33, # 47 p. 7245 - 7248 Title/Abstract Full Text View citing articles Show Details
Solladie-Cavallo, A.; Khiar, N.
Synthetic Communications, 1989 , vol. 19, # 7,8 p. 1335 - 1340 Title/Abstract Full Text Show Details
Sugawara, M.; Baizer, M. M.; Monte, W. T.; Little, R. D.; Hess, U.
Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry, 1983 , vol. 37, # 6 p. 509 - 518 Title/Abstract Full Text Show Details
Drewes, Siegfried E.; Manickum, Thavrin; Roos, Gregory H. P.
Synthetic Communications, 1988 , vol. 18, # 10 p. 1065 - 1070 Title/Abstract Full Text Show Details
Masuyama, Araki; Tsuchiya, Kikuo; Okahara, Mitsuo
Bulletin of the Chemical Society of Japan, 1985 , vol. 58, # 10 p. 2855 - 2859 Title/Abstract Full Text Show Details
Kano, Shinzo; Yuasa, Yoko; Shibuya, Shiroshi
Heterocycles, 1987 , vol. 26, # 2 p. 373 - 376 Title/Abstract Full Text View citing articles Show Details
23 of 63
24 of 63
Comment (Pharmacological Data)
Bioactivities present
Reference
Stachel; Drasch
Archiv der Pharmazie, 1985 , vol. 318, # 4 p. 304 - 311 Title/Abstract Full Text View citing articles Show Details
Creary, Xavier
Journal of the American Chemical Society, 1984 , vol. 106, # 19 p. 5568 - 5577 Title/Abstract Full Text View citing articles Show Details
Kluger, Ronald; Chow, Jane Frances; Croke, James J.
Journal of the American Chemical Society, 1984 , vol. 106, # 14 p. 4017 - 4020 Title/Abstract Full Text View citing articles Show Details
Baar, Ben L. M. van; Burgers, Peter C.; Holmes, John L.; Terlouw, Johan K.
Organic Mass Spectrometry, 1988 , vol. 23, p. 355 - 363 Title/Abstract Full Text Show Details
Toivonen, Hannu
Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry, 1984 , vol. 38, # 1 p. 37 - 42 Title/Abstract Full Text Show Details
Kurihara, Toshio; Sugizaki, Masaru; Kime, Itaru; Wada, Makoto; Mitsunobu, Oyo
Bulletin of the Chemical Society of Japan, 1981 , vol. 54, # 7 p. 2107 - 2112 Title/Abstract Full Text Show Details
Reetz, Manfred T.; Raguse, Burkhard; Seitz, Thomas
Tetrahedron, 1993 , vol. 49, # 38 p. 8561 - 8568 Title/Abstract Full Text View citing articles Show Details
Sugiyama, Shigeru; Shigemoto, Naoya; Masaoka, Naoki; Suetoh, Souichi; Kawami, Hideaki; et al.
Bulletin of the Chemical Society of Japan, 1993 , vol. 66, # 5 p. 1542 - 1547 Title/Abstract Full Text Show Details
Watanabe; Yoshiwara; Kanao
Journal of Heterocyclic Chemistry, 1993 , vol. 30, # 2 p. 445 - 451 Title/Abstract Full Text View citing articles Show Details
Bone, M. F.; Bradshaw, M. J.; Chan, L. K. M.; Coates, D.; Constant, J.; et al.
Molecular Crystals and Liquid Crystals (1969-1991), 1988 , vol. 164, p. 117 - 134 Title/Abstract Full Text Show Details
Koide, Naoyuki; Uehara, Keiichi; Iimura, Kazuyoshi
Molecular Crystals and Liquid Crystals (1969-1991), 1988 , vol. 157, p. 151 - 162 Title/Abstract Full Text Show Details
Kirby, Anthony J.; Walwyn, David R.
Gazzetta Chimica Italiana, 1987 , vol. 117, # 11 p. 667 - 680 Title/Abstract Full Text Show Details
Tawfik; Eshhar; Bentolila; Green
Synthesis, 1993 , # 10 p. 968 - 972 Title/Abstract Full Text View citing articles Show Details
Fukuzumi, Shonichi; Tokuda, Yoshihiro; Kitano, Toshiaki; Okamoto, Toshihiko; Otera, Junzo
Journal of the American Chemical Society, 1993 , vol. 115, # 20 p. 8960 - 8968 Title/Abstract Full Text View citing articles Show Details
Kolomeitsev; Chabanenko; Roschenthaler; Yagupolskii
Synthesis, 1994 , # 2 p. 145 - 146 Title/Abstract Full Text View citing articles Show Details
Molander, Gary A.; McKie, Jeffrey A.
Journal of Organic Chemistry, 1993 , vol. 58, # 25 p. 7216 - 7227 Title/Abstract Full Text View citing articles Show Details
Ohta, Hiromichi; Ozaki, Kazuhiko; Konishi, Jin; Tsuchihashi, Gen-ichi
Agricultural and Biological Chemistry, 1986 , vol. 50, # 5 p. 1261 - 1266 Title/Abstract Full Text Show Details
Laimer; Erker
Scientia Pharmaceutica, 1994 , vol. 62, # 1 p. 39 - 49 Title/Abstract Full Text View citing articles Show Details
Davis, Frank; Neogi, Partha; Stirling, Charles J. M.
Journal of the Chemical Society, Chemical Communications, 1994 , # 10 p. 1199 - 1200 Title/Abstract Full Text View citing articles Show Details
Puschmann, I.; Erker, T.
Monatshefte fuer Chemie, 1994 , vol. 125, # 8/9 p. 927 - 932 Title/Abstract Full Text View citing articles Show Details
Comment (Pharmacological Data)
Bioactivities present
Reference
Maekawa, Hirofumi; Ishino, Yoshio; Nishiguchi, Ikuzo
Chemistry Letters, 1994 , # 6 p. 1017 - 1020 Title/Abstract Full Text Show Details
Feldberg, Liron; Sasson, Yoel
Journal of the Chemical Society, Chemical Communications, 1994 , # 15 p. 1807 - 1808 Title/Abstract Full Text View citing articles Show Details
Spencer, Alwyn
Journal of Organometallic Chemistry, 1985 , vol. 295, p. 79 - 90 Title/Abstract Full Text View citing articles Show Details
Tanabe, Yoo; Okumura, Hitomi; Maeda, Akihiro; Murakami, Masanari
Tetrahedron Letters, 1994 , vol. 35, # 45 p. 8413 - 8414 Title/Abstract Full Text View citing articles Show Details
Morikawa, Tsutomu; Washio, Yoshiaki; Harada, Susumu; Hanai, Ryo; Kayashita, Takashi; et al.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1995 , # 3 p. 271 - 282 Title/Abstract Full Text View citing articles Show Details
Wu; Griffith; Loch III; Kover; Murray; Mullen; Blosser; Machulskis; McCreedy
Journal of Medicinal Chemistry, 1995 , vol. 38, # 9 p. 1558 - 1570
Title/Abstract Full Text View citing articles Show Details
Aurich; Biesemeier
Synthesis, 1995 , # 9 p. 1171 - 1178 Title/Abstract Full Text View citing articles Show Details
Tsukamoto; Fujii; Yasunaga; Matsuda; Wanibuchi; Hidaka; Furuya; Tamura
Chemical and Pharmaceutical Bulletin, 1995 , vol. 43, # 5 p. 842 - 852 Title/Abstract Full Text View citing articles Show Details
Kano, Yoshikazu; Minami, Ryuichi; Takahashi, Hiroaki
Bulletin of the Chemical Society of Japan, 1980 , vol. 53, # 3 p. 642 - 644 Title/Abstract Full Text Show Details
Katagiri, Toshimasa; Yoda, Chika; Furuhashi, Keizo; Ueki, Katsuyuki; Kubota, Toshio
Chemistry Letters, 1996 , # 2 p. 115 - 116 Title/Abstract Full Text View citing articles Show Details
Terfort, Andreas; Brunner, Henri
Journal of the Chemical Society - Perkin Transactions 1, 1996 , # 12 p. 1467 - 1479 Title/Abstract Full Text View citing articles Show Details
Loeffler; Schobert
Journal of the Chemical Society - Perkin Transactions 1, 1996 , # 23 p. 2799 - 2802 Title/Abstract Full Text View citing articles Show Details
Witty, David R.; Walker, Graham; Bateson, John H.; O'Hanlon, Peter J.; Cassels, Robert
Bioorganic and Medicinal Chemistry Letters, 1996 , vol. 6, # 12 p. 1375 - 1380 Title/Abstract Full Text View citing articles Show Details
Maugard, Thierry; Remaud-Simeon, Magali; Petre, Dominique; Monsan, Pierre
Tetrahedron, 1997 , vol. 53, # 14 p. 5185 - 5194 Title/Abstract Full Text View citing articles Show Details
Lewinski, Janusz; Zachara, Janusz; Justyniak, Iwona
Chemical Communications, 1997 , # 16 p. 1519 - 1520 Title/Abstract Full Text View citing articles Show Details
Zaleska; Krasodomski; Lis
Synthetic Communications, 1997 , vol. 27, # 13 p. 2337 - 2343 Title/Abstract Full Text View citing articles Show Details
Wang; Mallat; Baiker
Tetrahedron Asymmetry, 1997 , vol. 8, # 13 p. 2133 - 2140 Title/Abstract Full Text View citing articles Show Details
Fukuyama, Tohru; Cheung, Mui; Jow, Chung-Kuang; Hidai, Yuko; Kan, Toshiyuki
Tetrahedron Letters, 1997 , vol. 38, # 33 p. 5831 - 5834 Title/Abstract Full Text View citing articles Show Details
Asao, Naoki; Shimada, Takashi; Sudo, Tomoko; Tsukada, Naofumi; Yazawa, Kazuhiko; Gyoung, Young Soo; Uyehara, Tadao; Yamamoto, Yoshinori
Journal of Organic Chemistry, 1997 , vol. 62, # 18 p. 6274 - 6282 Title/Abstract Full Text View citing articles Show Details
Rojas-Garbanzo, Raul E.; Mata-Segreda, Julio F.
Bioorganic and Medicinal Chemistry Letters, 1998 , vol. 8, # 1 p. 7 - 10 Title/Abstract Full Text View citing articles Show Details
25 of 63
Comment (Pharmacological Data)
Bioactivities present
Reference
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Comment (Pharmacological Data)
Bioactivities present
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Comment (Pharmacological Data)
Bioactivities present
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Bioactivities present
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Comment (Pharmacological Data)
Bioactivities present
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Comment (Pharmacological Data)
Bioactivities present
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Comment (Pharmacological Data)
Bioactivities present
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Comment (Pharmacological Data)
Bioactivities present
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Hernández-Cortés, Guillermo; Valle-Rodríguez, Juan Octavio; Herrera-López, Enrique J.; Díaz-Montaño, Dulce María; González-García, Yolanda; EscalonaBuendía, Héctor B.; Córdova, Jesús
AMB Express, 2016 , vol. 6, # 1 art. no. 47 Title/Abstract Full Text View citing articles Show Details
Abou-Shehada, Sarah; Clark, James H.; Paggiola, Giulia; Sherwood, James
Chemical Engineering and Processing: Process Intensification, 2016 , vol. 99, p. 88 - 96 Title/Abstract Full Text View citing articles Show Details
Zhang, Xiaopeng; Wang, Hua; Liu, Xiao; Han, Jinyu; Zhu, Xinli; Ge, Qingfeng
Microporous and Mesoporous Materials, 2016 , vol. 233, p. 184 - 193 Title/Abstract Full Text View citing articles Show Details
Zhang, Xiaopeng; Wang, Hua; Liu, Xiao; Han, Jinyu; Zhu, Xinli; Ge, Qingfeng
Microporous and Mesoporous Materials, 2016 , vol. 233, p. 184 - 193 Title/Abstract Full Text View citing articles Show Details
Matsuda, Hiroyuki; Inaba, Koji; Sumida, Hirofumi; Kurihara, Kiyofumi; Tochigi, Katsumi; Ochi, Kenji
Fluid Phase Equilibria, 2015 , vol. 420, p. 50 - 57 Title/Abstract Full Text View citing articles Show Details
Ruddarraju, Radhakrishnam Raju; Murugulla, Adharvana Chari; Kotla, Ravindar; Chandra Babu Tirumalasetty, Muni; Wudayagiri, Rajendra; Donthabakthuni, Shobha; Maroju, Ravichandar; Baburao; Parasa, Lakshmana Swamy
European Journal of Medicinal Chemistry, 2016 , vol. 123, p. 379 - 396 Title/Abstract Full Text View citing articles Show Details
Lu, Yuyun; Chua, Jian-Yong; Huang, Dejian; Lee, Pin-Rou; Liu, Shao-Quan
Food Chemistry, 2017 , vol. 215, p. 209 - 218 Title/Abstract Full Text View citing articles Show Details
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Bioresource Technology, 2016 , vol. 219, p. 281 - 288 Title/Abstract Full Text View citing articles Show Details
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Energy and Fuels, 2016 , vol. 30, # 7 p. 5269 - 5276 Title/Abstract Full Text Show Details
Strati; Oreopoulou
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Strati; Oreopoulou
Waste and Biomass Valorization, 2016 , vol. 7, # 4 p. 843 - 850 Title/Abstract Full Text Show Details
Sun, Weining; Xiao, Huazhi; Peng, Qian; Zhang, Qiaoge; Li, Xingxing; Han, Ye
Annals of Microbiology, 2016 , vol. 66, # 3 p. 1293 - 1301 Title/Abstract Full Text View citing articles Show Details
Li, Qingyin; Liu, Dong; Hou, Xulian; Wu, Pingping; Song, Linhua; Yan, Zifeng
Bioresource Technology, 2016 , vol. 219, p. 281 - 288 Title/Abstract Full Text Show Details
Kua, Yin Leng; Gan, Suyin; Morris, Andrew; Ng, Hoon Kiat
Sustainable Chemistry and Pharmacy, 2016 , vol. 4, p. 21 - 31 Title/Abstract Full Text View citing articles Show Details
Rayne, Sierra; Forest, Kaya
Flavour and Fragrance Journal, 2016 , vol. 31, # 5 p. 385 - 394 Title/Abstract Full Text View citing articles Show Details
Petrus, Rafal; Bykowski, Dominik; Sobota, Piotr
ACS Catalysis, 2016 , vol. 6, # 8 p. 5222 - 5235 Title/Abstract Full Text View citing articles Show Details
Liu, Ning; Qin, Yi; Song, Yu-Yang; Tao, Yong-Sheng; Sun, Yue; Liu, Yan-Lin
International Journal of Food Properties, 2016 , vol. 19, # 11 p. 2417 - 2431 Title/Abstract Full Text View citing articles Show Details
Xing-lin, Han; Shi-ru, Jia; Wu-jiu, Zhang
Journal of the Institute of Brewing, 2016 , vol. 122, # 3 p. 397 - 402 Title/Abstract Full Text View citing articles Show Details
González-Robles, Ivonne Wendolyne; Cook, David J.
Journal of the Institute of Brewing, 2016 , vol. 122, # 3 p. 369 - 380 Title/Abstract Full Text View citing articles Show Details
Comment (Pharmacological Data)
Bioactivities present
Reference
Jiang, Zhu Mao; Chen, Yao; Wang, De Liang; Wang, Xu Liang; Shang, Ke; Zhang, Song; Li, Yao Yao
Journal of the Institute of Brewing, 2016 , vol. 122, # 3 p. 468 - 472 Title/Abstract Full Text View citing articles Show Details
Tan, Li; Yuan, Hua-Wei; Wang, Yan-Fang; Chen, Hao; Sun, Zhao-Yong; Tang, Yue-Qin; Kida, Kenji
Journal of the Institute of Brewing, 2016 , vol. 122, # 3 p. 486 - 492 Title/Abstract Full Text View citing articles Show Details
Lee, Sae-Byuk; Kim, Dong-Hwan; Park, Heui-Dong
Applied Microbiology and Biotechnology, 2016 , vol. 100, # 18 p. 7853 - 7863 Title/Abstract Full Text View citing articles Show Details
Kreethatorn, Hemmarat; Tantirungrotechai, Jonggol
Catalysis Communications, 2016 , vol. 86, p. 129 - 132 Title/Abstract Full Text Show Details
Zhang, Yanan; Sun, Baoguo; Sun, Jinyuan; Sun, Xiaotao; Huang, Mingquan; Li, Hehe
Shipin Kexue/Food Science, 2016 , vol. 37, # 16 p. 106 - 111
Title/Abstract Full Text Show Details
Bañuelos, Maria Antonia; Loira, Iris; Escott, Carlos; Del Fresno, Juan Manuel; Morata, Antonio; Sanz, Pedro D.; Otero, Laura; Suárez-Lepe, Jose Antonio
Food and Bioprocess Technology, 2016 , vol. 9, # 10 p. 1769 - 1778 Title/Abstract Full Text Show Details
Alaba, Peter Adeniyi; Sani, Yahaya Muhammad; Ashri Wan Daud, Wan Mohd
RSC Advances, 2016 , vol. 6, # 82 p. 78351 - 78368 Title/Abstract Full Text Show Details
Meza-Morelos, Dairo; Fernandez-Maestre, Roberto; Hill, Herbert H.
International Journal for Ion Mobility Spectrometry, 2016 , vol. 19, # 2-3 p. 145 - 153 Title/Abstract Full Text Show Details
Lee, Myeong Gi; Ham, Tae Hoon; Song, Sang Hoon; Chung, Dong Hwa; Yoon, Won Byong
Food Science and Biotechnology, 2016 , vol. 25, # 4 p. 1073 - 1080 Title/Abstract Full Text Show Details
Barbosa; Souza; Diniz; Godoy-Santos; Faria-Oliveira; Correa; Alvarez; Coutrim; Afonso; Castro; Brandão
Journal of Applied Microbiology, 2016 , vol. 121, # 4 p. 1038 - 1051 Title/Abstract Full Text Show Details
Gan, Xin; Lv, Ruitao; Zhu, Haoyue; Ma, Lai-Peng; Wang, Xuyang; Zhang, Zexia; Huang, Zheng-Hong; Zhu, Hongwei; Ren, Wencai; Terrones, Mauricio; Kang, Feiyu
Journal of Materials Chemistry A, 2016 , vol. 4, # 36 p. 13795 - 13802 Title/Abstract Full Text Show Details
Kong, Zhiqiang; Li, Minmin; An, Jingjing; Chen, Jieying; Bao, Yuming; Francis, Frédéric; Dai, Xiaofeng
Scientific Reports, 2016 , vol. 6, art. no. 33552 Title/Abstract Full Text Show Details
Anila; Rayapa Reddy; Srinivasa Rao; Sairam; Ramachandran; Rambabu
Journal of Chemical Thermodynamics, 2017 , vol. 104, p. 24 - 32 Title/Abstract Full Text Show Details
Anila; Rayapa Reddy; Srinivasa Rao; Sairam; Ramachandran; Rambabu
Journal of Chemical Thermodynamics, 2017 , vol. 104, p. 24 - 32 Title/Abstract Full Text Show Details
Wu, Lin-Huan; Lu, Zhen-Ming; Zhang, Xiao-Juan; Wang, Zong-Min; Yu, Yong-Jian; Shi, Jin-Song; Xu, Zheng-Hong
Food Microbiology, 2017 , vol. 62, p. 23 - 31 Title/Abstract Full Text Show Details
Park, Boyoung Y.; Luong, Tom; Sato, Hiroki; Krische, Michael J.
Journal of Organic Chemistry, 2016 , vol. 81, # 18 p. 8585 - 8594 Title/Abstract Full Text Show Details
Uekane, Thais M.; Nicolotti, Luca; Griglione, Alessandra; Bizzo, Humberto R.; Rubiolo, Patrizia; Bicchi, Carlo; Rocha-Leão, Maria Helena M.; Rezende, Claudia M.
Food Chemistry, 2017 , vol. 219, p. 13 - 22 Title/Abstract Full Text Show Details
Lu, Yuyun; Chua, Jian-Yong; Huang, Dejian; Lee, Pin-Rou; Liu, Shao-Quan
Applied Microbiology and Biotechnology, 2016 , vol. 100, # 20 p. 8877 - 8888 Title/Abstract Full Text Show Details
Benito, Ángel; Calderón, Fernando; Palomero, Felipe; Benito, Santiago
Food Technology and Biotechnology, 2016 , vol. 54, # 2 p. 135 - 144 Title/Abstract Full Text Show Details
Pang, Qingqing; Wang, Deyan; Wang, Xiuyan; Feng, Shaoguang; Clark, Michael B.; Li, Qiaowei
ACS Applied Materials and Interfaces, 2016 , vol. 8, # 38 p. 25469 - 25475 Title/Abstract Full Text Show Details
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Comment (Pharmacological Data)
Bioactivities present
Reference
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, 2014 , vol. 28, # 21 p. 1887 - 1893 Title/Abstract Full Text Show Details
SAGAMI CHEMICAL RESEARCH INSTITUTE; KAKEN PHARMACEUTICAL COMPANY LIMITED; KOBAYASHI, OSAMU; TAKATSUNA, REIKO; NIIKURA, NAOKO; MATSUKAWA, TOMOKO; NAKAMURA, SHINJI; HIRAI, KENJI; KOCHI, SHINICHIRO; KAWANISHI, NAOKI; YAMADA, OSAMU
Patent: JP2016/56158 A, 2016 ; Title/Abstract Full Text Show Details
Binczarski; Berlowska; Stanishevsky; Witonska
RSC Advances, 2016 , vol. 6, # 95 p. 92420 - 92427 Title/Abstract Full Text Show Details
Frutiger, Jérôme; Marcarie, Camille; Abildskov, Jens; Sin, Gürkan
Journal of Hazardous Materials, 2016 , vol. 318, p. 783 - 793 Title/Abstract Full Text Show Details
Pedneault, Karine; Provost, Caroline
Scientia Horticulturae, 2016 , vol. 208, p. 57 - 77 Title/Abstract Full Text Show Details
Maru; López; Kengen; Constantí; Medina
Fuel, 2016 , vol. 186, p. 375 - 384 Title/Abstract Full Text Show Details
Wang, Liang; Zhong, Hao; Liu, Keying; Guo, Aizhen; Qi, Xianghui; Cai, Meihong
Food Science and Technology International, 2016 , vol. 22, # 7 p. 598 - 608 Title/Abstract Full Text Show Details
Ramírez, Manuel; Velázquez, Rocío; Maqueda, Matilde; Zamora, Emiliano; López-Piñeiro, Antonio; Hernández, Luis M.
International Journal of Food Microbiology, 2016 , vol. 238, p. 311 - 319 Title/Abstract Full Text Show Details
Rodríguez-Bencomo, Juan José; Pérez-Correa, José Ricardo; Orriols, Ignacio; López, Francisco
Food and Bioprocess Technology, 2016 , vol. 9, # 11 p. 1885 - 1892 Title/Abstract Full Text Show Details
Suriano; Alba; Di Gennaro; Basile; Tamborra; Tarricone
Journal of Food Science and Technology, 2016 , vol. 53, # 8 p. 3329 - 3339 Title/Abstract Full Text Show Details
Ugur Nigiz; Durmaz Hilmioglu
Chemical and Biochemical Engineering Quarterly, 2016 , vol. 30, # 3 p. 381 - 391
Title/Abstract Full Text Show Details
Winoto, Haryo Pandu; Ahn, Byoung Sung; Jae, Jungho
Journal of Industrial and Engineering Chemistry, 2016 , vol. 40, p. 62 - 71 Title/Abstract Full Text Show Details
Scriba, Gerhard K.E.
Journal of Chromatography A, 2016 , vol. 1467, p. 56 - 78 Title/Abstract Full Text Show Details
Weiss; Kroschewski; Auerbach
Journal of Dairy Science, 2016 , vol. 99, # 10 p. 8053 - 8069 Title/Abstract Full Text Show Details
Sánchez-Camargo; Montero; Cifuentes; Herrero; Ibáñez
RSC Advances, 2016 , vol. 6, # 97 p. 94884 - 94895 Title/Abstract Full Text Show Details
Maru; López; Kengen; Constantí; Medina
Fuel, 2016 , vol. 186, p. 375 - 384 Title/Abstract Full Text Show Details
Frutiger, Jérôme; Marcarie, Camille; Abildskov, Jens; Sin, Gürkan
Journal of Hazardous Materials, 2016 , vol. 318, p. 783 - 793 Title/Abstract Full Text Show Details
Birkenmeier, Gerd; Hemdan, Nasr Y.A.; Kurz, Susanne; Bigl, Marina; Pieroh, Philipp; Debebe, Tewodros; Buchold, Martin; Thieme, Rene; Wichmann, Gunnar; Dehghani, Faramarz
PLoS ONE, 2016 , vol. 11, # 8 art. no. E0161571 Title/Abstract Full Text Show Details
Rao, P. Sankara; Srihari
Organic and Biomolecular Chemistry, 2016 , vol. 14, # 40 p. 9629 - 9638 Title/Abstract Full Text Show Details
Nisol, Bernard; Watson, Sean; Lerouge, Sophie; Wertheimer, Michael R.
Plasma Processes and Polymers, 2016 , vol. 13, # 10 p. 965 - 969 Title/Abstract Full Text Show Details
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Comment (Pharmacological Data)
Bioactivities present
Reference
Motta, Silvia; Guaita, Massimo; Petrozziello, Maurizio; Ciambotti, Aldo; Panero, Loretta; Solomita, Mauro; Bosso, Antonella
Food Chemistry, 2017 , vol. 221, p. 1 - 10 Title/Abstract Full Text Show Details
Pereira, Vanda; Santos, Magda; Cacho, Juan; Marques, José C.
LWT - Food Science and Technology, 2017 , vol. 75, p. 719 - 726 Title/Abstract Full Text Show Details
Crowley-Gall, Amber; Date, Priya; Han, Clair; Rhodes, Nicole; Andolfatto, Peter; Layne, John E.; Rollmann, Stephanie M.
Proceedings of the Royal Society B: Biological Sciences, 2016 , vol. 283, # 1837 art. no. 20161562 Title/Abstract Full Text Show Details
Yuan, Guanshen; Ren, Jie; Ouyang, Xiaoyu; Wang, Liying; Wang, Mengze; Shen, Xiaodong; Zhang, Bolin; Zhu, Baoqing
Molecules, 2016 , vol. 21, # 10 art. no. 1324 Title/Abstract Full Text Show Details
Jain, Anjali; Doppalapudi, Sindhu; Domb, Abraham J.; Khan, Wahid
Journal of Controlled Release, 2016 , vol. 243, p. 132 - 145 Title/Abstract Full Text Show Details
Li, Zhen; Liu, Xianwei; Lian, Yiwei; Xie, Juan; Gao, Xiaorui; Chang, Tao
World Journal of Engineering, 2016 , vol. 13, # 2 p. 142 - 148 Title/Abstract Full Text Show Details
Duan, Hailing; Yamada, Yasuhiro; Sato, Satoshi
Chemistry Letters, 2016 , vol. 45, # 9 p. 1036 - 1047 Title/Abstract Full Text Show Details
Sathish; Silambarasan; Madhan; Raghava Rao
Green Chemistry, 2016 , vol. 18, # 21 p. 5806 - 5813 Title/Abstract Full Text Show Details
Liu, Yi; Wu, Qiong; Wu, Qingyuan; Jiang, Heti
Shipin Kexue/Food Science, 2016 , vol. 37, # 20 p. 108 - 112 Title/Abstract Full Text Show Details
Comment (Pharmacological Data)
physiological behaviour discussed
Reference
OLFACTOR LABORATORIES, INC.; FRUTOS, Ulises; ELKASHEF, Samer; BROWN, Michelle Ardella
Patent: WO2015/116801 A2, 2015 ; Title/Abstract Full Text Show Details
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Location
Page/Page column
Comment (Pharmacological Data)
physiological behaviour discussed
Reference
OLFACTOR LABORATORIES INCORPORATED; BROWN, Michelle, Ardella; LOMELI, Martin, Antonio, Jr.; ELKASHEF, Samer; ZION, Tricia; FRUTOS, Ulises
Patent: WO2014/28835 A2, 2014 ; Title/Abstract Full Text Show Details
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Effect (Pharmacological Data)
insecticidal
Species or Test-System (Pharmacological Data)
German cockroach SCJ Strain
Sex
female
Kind of Dosing (Pharmacological Data)
title compound formulated with acetone
Method (Pharmacological Data)
In this example, the effectiveness of compositions comprising various concentrations of mineral oil and/or ethyl lactate at killing German cockroachs was tested.To begin, compositions comprising mineral oil and/or ethyl lactate in the following concentrations were prepared: 100percent (wt/wt) mineral oil/0percent (wt/wt) ethyl lactate; 90percent (wt/wt) mineral oil/10percent (wt/wt) ethyl lactate; 75percent (wt/wt) mineral oil/25percent (wt/wt) ethyl lactate; 50percent (wt/wt) mineral oil/50percent (wt/wt) ethyl lactate; 25percent (wt/wt) mineral oil/75percent (wt/wt) ethyl lactate; 10percent (wt/wt) mineral oil/90percent (wt/wt) ethyl lactate; 0percent (wt/wt) mineral oil/100percent (wt/wt) ethyl lactate. The ethyl lactate was obtained from Vertech Biosolvents, Inc., Downers Grove, Ill.Prior to testing, each composition containing either mineral oil, ethyl lactate, or a combination of mineral oil and ethyl lactate was diluted by 50percent by mixing the composition with acetone in a 1:1 ratio (wt/wt) to reduce viscosity prior to application of the compositions to the cockroachs. The amount of mineral oil, ethyl lactate, and acetone present in the final composition (A-G) is set forth below in Table 1.Toxicity evaluations were performed on 7-14 day old adult male and female German cockroachs (SCJ Strain, S.C. Johnson Son, Racine, Wis.). Approximately 12 cockroachs were transferred to individual 100.x.20 mm polystyrene Petri dishes and anesthetized with a 15-25 second exposure to carbon dioxide. The inside edge of each Petri dish was lightly coated with mineral oil plus petroleum jelly in a 1:3 (wt/wt) ratio to minimize escape. Anesthetized cockroachs were positioned with their ventral side up, and a 1 μl drop of the diluted test composition was applied to the area between the meso- and metathoracic legs using a Rainin L-10, 10 μl capacity pipette (Rainin Instrument, LLC, Oakland, Calif.). Five replications of 12 male cockroachs were done for each test composition. Separate tests were done using female cockroachs. Results were evaluated at 24 hours following treatment. Cockroaches were scored as either alive (dorsal side up, active movement when abdomen prodded with dissecting probe) or moribund/dead (dorsal side up and no movement when abdomen prodded or ventral side up and insect unable to right itself).Results are shown in FIG. 1 and Table 1, which lists the number of dead cockroachs out of 60 total cockroachs for each test performed using the diluted test compositions (A-G).
Location
Page/Page column 7
Comment (Pharmacological Data)
potential area of application: agro No effect
Reference
Whitmire Micro-Gen Research Laboratories, Inc.
Patent: US2009/257958 A1, 2009 ; Title/Abstract Full Text Show Details
46 of 63
Effect (Pharmacological Data)
insecticidal
Species or Test-System (Pharmacological Data)
German cockroach SCJ Strain
Sex
male
Kind of Dosing (Pharmacological Data)
title compound formulated with acetone
Method (Pharmacological Data)
In this example, the effectiveness of compositions comprising various concentrations of mineral oil and/or ethyl lactate at killing German cockroachs was tested.To begin, compositions comprising mineral oil and/or ethyl lactate in the following concentrations were prepared: 100percent (wt/wt) mineral oil/0percent (wt/wt) ethyl lactate; 90percent (wt/wt) mineral oil/10percent (wt/wt) ethyl lactate; 75percent (wt/wt) mineral oil/25percent (wt/wt) ethyl lactate; 50percent (wt/wt) mineral oil/50percent (wt/wt) ethyl lactate; 25percent (wt/wt) mineral oil/75percent (wt/wt) ethyl lactate; 10percent (wt/wt) mineral oil/90percent (wt/wt) ethyl lactate; 0percent (wt/wt) mineral oil/100percent (wt/wt) ethyl lactate. The ethyl lactate was obtained from Vertech Biosolvents, Inc., Downers Grove, Ill.Prior to testing, each composition containing either mineral oil, ethyl lactate, or a combination of mineral oil and ethyl lactate was diluted by 50percent by mixing the composition with acetone in a 1:1 ratio (wt/wt) to reduce viscosity prior to application of the compositions to the cockroachs. The amount of mineral oil, ethyl lactate, and acetone present in the final composition (A-G) is set forth below in Table 1.Toxicity evaluations were performed on 7-14 day old adult male and female German cockroachs (SCJ Strain, S.C. Johnson Son, Racine, Wis.). Approximately 12 cockroachs were transferred to individual 100.x.20 mm polystyrene Petri dishes and anesthetized with a 15-25 second exposure to carbon dioxide. The inside edge of each Petri dish was lightly coated with mineral oil plus petroleum jelly in a 1:3 (wt/wt) ratio to minimize escape. Anesthetized cockroachs were positioned with their ventral side up, and a 1 μl drop of the diluted test composition was applied to the area between the meso- and metathoracic legs using a Rainin L-10, 10 μl capacity pipette (Rainin Instrument, LLC, Oakland, Calif.). Five replications of 12 male cockroachs were done for each test composition. Separate tests were done using female cockroachs. Results were evaluated at 24 hours following treatment. Cockroaches were scored as either alive (dorsal side up, active movement when abdomen prodded with dissecting probe) or moribund/dead (dorsal side up and no movement when abdomen prodded or ventral side up and insect unable to right itself).Results are shown in FIG. 1 and Table 1, which lists the number of dead cockroachs out of 60 total cockroachs for each test performed using the diluted test compositions (A-G).
Results
dead insects (number) = 3 out of 60 at 50percent
Location
Page/Page column 7
Comment (Pharmacological Data)
potential area of application: agro
Reference
Whitmire Micro-Gen Research Laboratories, Inc.
Patent: US2009/257958 A1, 2009 ; Title/Abstract Full Text Show Details
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Effect (Pharmacological Data)
cytokine release; inhibition of
Species or Test-System (Pharmacological Data)
human blood
Concentration (Pharmacological Data)
1 - 20 mmol/l
Method (Pharmacological Data)
heparinized blood from healthy subjects incubated with title comp. in presence of lipopolysaccharide for 6 h at 37 deg C; tumor necrosis factor-α, IL-6, IL-1β, IL-8 levels determined
Further Details (Pharmacological Data)
control: without title comp.; IL: interleukin; reference comp.: p-bromobenzylglutathione cyclopentyl diester
Type (Pharmacological Data)
IC50
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Value of Type (Pharmacological Data)
4.93 - 10.43 mmol/l
Results
title comp. IC50s were 5.67/10.43/8.88/4.93 mM for tumor necrosis factor-α/IL-1β/IL-6/IL-8, resp.; fig.
Reference
Hollenbach, Marcus; Hintersdorf, Anja; Huse, Klaus; Sack, Ulrich; Bigl, Marina; Groth, Marco; Santel, Thore; Buchold, Martin; Lindner, Inge; Otto, Andreas; Sicker, Dieter; Schellenberger, Wolfgang; Almendinger, Johannes; Pustowoit, Barbara; Birkemeyer, Claudia; Platzer, Mathias; Oerlecke, Ilka; Hemdan, Nasr; Birkenmeier, Gerd
Biochemical Pharmacology, 2008 , vol. 76, # 5 p. 631 - 644 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
enzyme activity; effect on
Species or Test-System (Pharmacological Data)
human glyoxalase 1
Concentration (Pharmacological Data)
Ca. 2.5 - 20 mmol/l
Method (Pharmacological Data)
title comp. incubated with reduced glutathione; reaction started by adding methylglyoxal and enzyme; incubated for 4 min; glyoxalase-1 activity determined
Further Details (Pharmacological Data)
control: without title comp.
Comment (Pharmacological Data)
No effect
Reference
Hollenbach, Marcus; Hintersdorf, Anja; Huse, Klaus; Sack, Ulrich; Bigl, Marina; Groth, Marco; Santel, Thore; Buchold, Martin; Lindner, Inge; Otto, Andreas; Sicker, Dieter; Schellenberger, Wolfgang; Almendinger, Johannes; Pustowoit, Barbara; Birkemeyer, Claudia; Platzer, Mathias; Oerlecke, Ilka; Hemdan, Nasr; Birkenmeier, Gerd
Biochemical Pharmacology, 2008 , vol. 76, # 5 p. 631 - 644 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
immunosuppressant
Species or Test-System (Pharmacological Data)
peripheral blood mononuclear cells of human
Concentration (Pharmacological Data)
1 - 10 mmol/l
Method (Pharmacological Data)
cells of rubella-infected subjects were re-stimulated with recombinant rubella-like particles and PHA in presence of title comp. for 18 h at 37 deg C; washed; T helper 1 cell response visualized by IFN-γ positive spots was analyzed by ELISPOT assay
Further Details (Pharmacological Data)
control: without title comp.; PHA: phytohemagglutinin; IFN-γ: interferon-γ
Results
title comp. decreased the number of IFN-γ positive spots; at 10 mM, suppressed the T helper 1 cell response by ca. 90percent; fig.
Reference
Hollenbach, Marcus; Hintersdorf, Anja; Huse, Klaus; Sack, Ulrich; Bigl, Marina; Groth, Marco; Santel, Thore; Buchold, Martin; Lindner, Inge; Otto, Andreas; Sicker, Dieter; Schellenberger, Wolfgang; Almendinger, Johannes; Pustowoit, Barbara; Birkemeyer, Claudia; Platzer, Mathias; Oerlecke, Ilka; Hemdan, Nasr; Birkenmeier, Gerd
Biochemical Pharmacology, 2008 , vol. 76, # 5 p. 631 - 644 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
cytotoxicity
Species or Test-System (Pharmacological Data)
peripheral blood mononuclear cells of human
Concentration (Pharmacological Data)
1 - 10 mmol/l
Method (Pharmacological Data)
cells of rubella-infected subjects were re-stimulated with recombinant rubella-like particles and PHA in presence of title comp. for 18 h at 37 deg C; incub. with trypan blue; cell viability detd. by measuring trypan blue exclusion using hemacytometer
Further Details (Pharmacological Data)
control: without title comp.; PHA: phytohemagglutinin
Comment (Pharmacological Data)
No effect
Reference
Hollenbach, Marcus; Hintersdorf, Anja; Huse, Klaus; Sack, Ulrich; Bigl, Marina; Groth, Marco; Santel, Thore; Buchold, Martin; Lindner, Inge; Otto, Andreas; Sicker, Dieter; Schellenberger, Wolfgang; Almendinger, Johannes; Pustowoit, Barbara; Birkemeyer, Claudia; Platzer, Mathias; Oerlecke, Ilka; Hemdan, Nasr; Birkenmeier, Gerd
Biochemical Pharmacology, 2008 , vol. 76, # 5 p. 631 - 644 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
cytokine level; effect on
Species or Test-System (Pharmacological Data)
peripheral blood mononuclear cells of human
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Concentration (Pharmacological Data)
1 - 10 mmol/l
Method (Pharmacological Data)
cells of rubella-infected subjects were re-stimulated with phytohemagglutinin in presence of title comp. for 18 h at 37 deg C; IL-2, interferon-γ, tumor necrosis factor-α, IL-4, IL-5, IL-6 and IL-10 levels determined
Further Details (Pharmacological Data)
control: without title comp.; IL-2/-4/-5/-6/-10: interleukin-2/-4/-5/-6/-10, respectively
Results
title comp. reduced T helper cell activation and attenuated the release of interferon-γ, IL-2, tumor necrosis factor-α and IL-10 while no detectable levels of IL-4 or IL-5 were found; table
Reference
Hollenbach, Marcus; Hintersdorf, Anja; Huse, Klaus; Sack, Ulrich; Bigl, Marina; Groth, Marco; Santel, Thore; Buchold, Martin; Lindner, Inge; Otto, Andreas; Sicker, Dieter; Schellenberger, Wolfgang; Almendinger, Johannes; Pustowoit, Barbara; Birkemeyer, Claudia; Platzer, Mathias; Oerlecke, Ilka; Hemdan, Nasr; Birkenmeier, Gerd
Biochemical Pharmacology, 2008 , vol. 76, # 5 p. 631 - 644 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
cyclin D1 expression; effect on
Species or Test-System (Pharmacological Data)
Hela cells
Method (Pharmacological Data)
Examples32D cl 3 cells were incubated: 1) in the absence of any added compounds; 2) in the presence of EUK- 134 or ethyl pyruvate for 1 hour before irradiation; 3) in the presence of ethyl pyruvate in methyl cellulose following irradiation; or 4) in the presence of ethyl pyruvate for 1 hour before irradiation and also in the presence of ethyl pyruvate in methylcellulose following irradiation. For EUK-134 (Eukarion, Inc., Bedford, MA), 32D cl 3 cells were incubated for 1 hour in the presence of 100 μM concentration of EUK-134, or 100 μM tempol as a control, and plated in methylcellulose. In the case of ethyl pyruvate, cells were incubated for 1 hour in the presence of 20 mM ethyl pyruvate. In all groups, cells were irradiated to doses ranging from 0 to 800 cGy and incubated at 370C for 7 days at which time colonies of >50 cells were counted and the data analyzed by linear quadratic or single-hit, multi-target models.Cells incubated in EUK-134 had an increased shoulder on the survival curve with an n {i.e., the width of the shoulder region representing the quasi-threshold dose, or the point at which death becomes exponential) of 5.38 compared to an n of 1.43 for 32D cl 3 cells, as shown in Figure 1.32D cl 3 cells incubated in the presence of ethyl pyruvate 1 hour before irradiation or plated in methylcellulose containing ethyl pyruvate had an increased D0 (i.e., the dose required to reduce the surviving fraction to 37percent in the exponential portion of the survival curve), compared to 32D cells alone (2.20 +/- 0.25, 2.21 +/- 0.15, and 1.84 +/- 0.25 Gy, respectively) but no change in n (2.00 +/- 1.01, 1.11 + 0.12, or 1.70 +/- 0.37, respectively). The combination of incubating 32D cl 3 cells in ethyl pyruvate both before irradiation and in methylcellulose media after irradiation resulted in optimal radioprotection as shown by a significantly increased shoulder on the survival curve compared to untreated-irradiated 32D cl 3 cells (n = 4.14 +/- 1.59 and 1.70 +/- 0.6, respectively, p = 0.0485), as shown in Figure 2. Thus, ethyl pyruvate administered before and after irradiation resulted in increased radiation resistance and cells incubated in ethyl pyruvate either before or after irradiation also had an increased radiation resistance.To determine whether ethyl pyruvate prevents irradiation-induced apoptosis, 32D cl 3 cells were incubated in the presence of 20 mM ethyl pyruvate 1 hour before irradiation to 10 Gy. The cells were then placed in tissue culture media and incubated for 24 hours at 370C. The apoptotic cells were labeled with FITC-UTP using a Promega Dead End Fluorometric Tunel Assay. The cells were observed under a fluorescent microscope and the percent of EPO apoptotic cells determined. As shown in Figure 3, ethyl pyruvate decreased the percent of 32D cl 3 cells undergoing irradiation apoptosis. Twenty-four hours after 10 Gy irradiation, cells incubated for 1 hour in ethyl pyruvate had 2.8 +/- 0.7percent (p<0.0001) apoptotic cells (1.2 +/- 0.5percent for non-irradiated cells) compared to 23.7 +/- 1.8percent for irradiated cells. Thus, incubation of cells in the presence of ethyl pyruvate before irradiation resulted in decreased percent of apoptotic cells.32D cl 3 cells were also incubated for 1 hour with 5 mM ethyl pyruvate or 100 μM tempol, as a control medium. The cells were then irradiated to doses ranging from 0 to 800 cGy and plated in methylcellulose. After 7 days, colonies of greater than 50 cells were counted. The Do of cells incubated with ethyl pyruvate was 1.466 Gy compared to 0.797 Gy for control 32D cl 3 cells (Figure 4).To determine whether ethyl pyruvate protects cells in vivo, C57BL/6NHsd female mice at 7-8 weeks of age were divided into five groups (10 mice per group) which received: 1) 9 Gy whole body irradiation only; 2) intravenous (IV) injections of MnSOD-PL (200 μg plasmid DNA) 24 hours before irradiation of 9 Gy whole body; 3) ethyl pyruvate (70 mg/kg) 30 minutes b
Location
Page/Page column 5; 8-11; 5/5
Comment (Pharmacological Data)
No effect
Reference
UNIVERSITY OF PITTSBURGH - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION
Patent: WO2007/14237 A2, 2007 ; Title/Abstract Full Text Show Details
53 of 63
Effect (Pharmacological Data)
cyclin D1 expression; effect on
Species or Test-System (Pharmacological Data)
MCF7 cells
Method (Pharmacological Data)
Examples32D cl 3 cells were incubated: 1) in the absence of any added compounds; 2) in the presence of EUK- 134 or ethyl pyruvate for 1 hour before irradiation; 3) in the presence of ethyl pyruvate in methyl cellulose following irradiation; or 4) in the presence of ethyl pyruvate for 1 hour before irradiation and also in the presence of ethyl pyruvate in methylcellulose following irradiation. For EUK-134 (Eukarion, Inc., Bedford, MA), 32D cl 3 cells were incubated for 1 hour in the presence of 100 μM concentration of EUK-134, or 100 μM tempol as a control, and plated in methylcellulose. In the case of ethyl pyruvate, cells were incubated for 1 hour in the presence of 20 mM ethyl pyruvate. In all groups, cells were irradiated to doses ranging from 0 to 800 cGy and incubated at 370C for 7 days at which time colonies of >50 cells were counted and the data analyzed by linear quadratic or single-hit, multi-target models.Cells incubated in EUK-134 had an increased shoulder on the survival curve with an n {i.e., the width of the shoulder region representing the quasi-threshold dose, or the point at which death becomes exponential) of 5.38 compared to an n of 1.43 for 32D cl 3 cells, as shown in Figure 1.32D cl 3 cells incubated in the presence of ethyl pyruvate 1 hour before irradiation or plated in methylcellulose containing ethyl pyruvate had an increased D0 (i.e., the dose required to reduce the surviving fraction to 37percent in the exponential portion of the survival curve), compared to 32D cells alone (2.20 +/- 0.25, 2.21 +/- 0.15, and 1.84 +/- 0.25 Gy, respectively) but no change in n (2.00 +/- 1.01, 1.11 + 0.12, or 1.70 +/- 0.37, respectively). The combination of incubating 32D cl 3 cells in ethyl pyruvate both before irradiation and in methylcellulose media after irradiation resulted in optimal radioprotection as shown by a significantly increased shoulder on the survival curve compared to untreated-irradiated 32D cl 3 cells (n = 4.14 +/- 1.59 and 1.70 +/- 0.6, respectively, p = 0.0485), as shown in Figure 2. Thus, ethyl pyruvate administered before and after irradiation resulted in increased radiation resistance and cells incubated in ethyl pyruvate either before or after irradiation also had an increased radiation resistance.To determine whether ethyl pyruvate prevents irradiation-induced apoptosis, 32D cl 3 cells were incubated in the presence of 20 mM ethyl pyruvate 1 hour before irradiation to 10 Gy. The cells were then placed in tissue culture media and incubated for 24 hours at 370C. The apoptotic cells were labeled with FITC-UTP using a Promega Dead End Fluorometric Tunel Assay. The cells were observed under a fluorescent microscope and the percent of EPO apoptotic cells determined. As shown in Figure 3, ethyl pyruvate decreased the percent of 32D cl 3 cells undergoing irradiation apoptosis. Twenty-four hours after 10 Gy irradiation, cells incubated for 1 hour in ethyl pyruvate had 2.8 +/- 0.7percent (p<0.0001) apoptotic cells (1.2 +/- 0.5percent for non-irradiated cells) compared to 23.7 +/- 1.8percent for irradiated cells. Thus, incubation of cells in the presence of ethyl pyruvate before irradiation resulted in decreased percent of apoptotic cells.32D cl 3 cells were also incubated for 1 hour with 5 mM ethyl pyruvate or 100 μM tempol, as a control medium. The cells were then irradiated to doses ranging from 0 to 800 cGy and plated in methylcellulose. After 7 days, colonies of greater than 50 cells were counted. The Do of cells incubated with ethyl pyruvate was 1.466 Gy compared to 0.797 Gy for control 32D cl 3 cells (Figure 4).To determine whether ethyl pyruvate protects cells in vivo, C57BL/6NHsd female mice at 7-8 weeks of age were divided into five groups (10 mice per group) which received: 1) 9 Gy whole body irradiation only; 2)
intravenous (IV) injections of MnSOD-PL (200 μg plasmid DNA) 24 hours before irradiation of 9 Gy whole body; 3) ethyl pyruvate (70 mg/kg) 30 minutes b Location
Page/Page column 5; 8-11; 5/5
Comment (Pharmacological Data)
No effect
Reference
UNIVERSITY OF PITTSBURGH - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION
Patent: WO2007/14237 A2, 2007 ; Title/Abstract Full Text Show Details
54 of 63
Effect (Pharmacological Data)
Phytotoxicity
Species or Test-System (Pharmacological Data)
apple
Method (Pharmacological Data)
Example 3 : Tests for Potential Phytotoxicity of Sprayed Aqueous Solvents; The potential for phytotoxicity (plant injury) by spraying 1 to 2percent aqueous solutions of ethyl lactate and solvent blends with ethyl lactate, as well as other ingredients such as glycerol and soy methyl esters was evaluated in field tests with apple trees and in greenhouse tests with corn, green bean, cucumber, tomato, ryegrass and hosta seedlings. The results showed no evidence of phytotoxicity for any of these solvent blends.In field tests with grapes this GA formulation with the solvent blend showed no adverse effects and gave the same results as to yield and performance as the control that used the standard 4percent GA in IPA formulation. EPO Each of the patents and articles cited herein is incorporated by reference. The use of the article "a" or "an" is intended to include one or more.
Location
Page/Page column 11
Comment (Pharmacological Data)
potential area of application: agro No effect
Reference
VERTEC BIOSOLVENTS, INC.
Patent: WO2006/65935 A2, 2006 ; Title/Abstract Full Text Show Details
55 of 63
Effect (Pharmacological Data)
Phytotoxicity
Species or Test-System (Pharmacological Data)
corn
Method (Pharmacological Data)
Example 3 : Tests for Potential Phytotoxicity of Sprayed Aqueous Solvents; The potential for phytotoxicity (plant injury) by spraying 1 to 2percent aqueous solutions of ethyl lactate and solvent blends with ethyl lactate, as well as other ingredients such as glycerol and soy methyl esters was evaluated in field tests with apple trees and in greenhouse tests with corn, green bean, cucumber, tomato, ryegrass and hosta seedlings. The results showed no evidence of phytotoxicity for any of these solvent blends.In field tests with grapes this GA formulation with the solvent blend showed no adverse effects and gave the same results as to yield and performance as the control that used the standard 4percent GA in IPA formulation. EPO Each of the patents and articles cited herein is incorporated by reference. The use of the article "a" or "an" is intended to include one or more.
Location
Page/Page column 11
Comment (Pharmacological Data)
potential area of application: agro No effect
Reference
VERTEC BIOSOLVENTS, INC.
Patent: WO2006/65935 A2, 2006 ; Title/Abstract Full Text Show Details
56 of 63
Effect (Pharmacological Data)
Phytotoxicity
Species or Test-System (Pharmacological Data)
green bean
Method (Pharmacological Data)
Example 3 : Tests for Potential Phytotoxicity of Sprayed Aqueous Solvents; The potential for phytotoxicity (plant injury) by spraying 1 to 2percent aqueous solutions of ethyl lactate and solvent blends with ethyl lactate, as well as other ingredients such as glycerol and soy methyl esters was evaluated in field tests with apple trees and in greenhouse tests with corn, green bean, cucumber, tomato, ryegrass and hosta seedlings. The results showed no evidence of phytotoxicity for any of these solvent blends.In field tests with grapes this GA formulation with the solvent blend showed no adverse effects and gave the same results as to yield and performance as the control that used the standard 4percent GA in IPA formulation. EPO Each of the patents and articles cited herein is incorporated by reference. The use of the article "a" or "an" is intended to include one or more.
Location
Page/Page column 11
Comment (Pharmacological Data)
potential area of application: agro No effect
Reference
VERTEC BIOSOLVENTS, INC.
Patent: WO2006/65935 A2, 2006 ; Title/Abstract Full Text Show Details
57 of 63
Effect (Pharmacological Data)
Phytotoxicity
Species or Test-System (Pharmacological Data)
cucumber
Method
Example 3 : Tests for Potential Phytotoxicity of Sprayed Aqueous Solvents; The potential for phytotoxicity (plant injury) by spraying 1 to 2percent aqueous solutions of ethyl
(Pharmacological Data)
lactate and solvent blends with ethyl lactate, as well as other ingredients such as glycerol and soy methyl esters was evaluated in field tests with apple trees and in greenhouse tests with corn, green bean, cucumber, tomato, ryegrass and hosta seedlings. The results showed no evidence of phytotoxicity for any of these solvent blends.In field tests with grapes this GA formulation with the solvent blend showed no adverse effects and gave the same results as to yield and performance as the control that used the standard 4percent GA in IPA formulation. EPO Each of the patents and articles cited herein is incorporated by reference. The use of the article "a" or "an" is intended to include one or more.
Location
Page/Page column 11
Comment (Pharmacological Data)
potential area of application: agro No effect
Reference
VERTEC BIOSOLVENTS, INC.
Patent: WO2006/65935 A2, 2006 ; Title/Abstract Full Text Show Details
58 of 63
Effect (Pharmacological Data)
Phytotoxicity
Species or Test-System (Pharmacological Data)
tomato
Method (Pharmacological Data)
Example 3 : Tests for Potential Phytotoxicity of Sprayed Aqueous Solvents; The potential for phytotoxicity (plant injury) by spraying 1 to 2percent aqueous solutions of ethyl lactate and solvent blends with ethyl lactate, as well as other ingredients such as glycerol and soy methyl esters was evaluated in field tests with apple trees and in greenhouse tests with corn, green bean, cucumber, tomato, ryegrass and hosta seedlings. The results showed no evidence of phytotoxicity for any of these solvent blends.In field tests with grapes this GA formulation with the solvent blend showed no adverse effects and gave the same results as to yield and performance as the control that used the standard 4percent GA in IPA formulation. EPO Each of the patents and articles cited herein is incorporated by reference. The use of the article "a" or "an" is intended to include one or more.
Location
Page/Page column 11
Comment (Pharmacological Data)
potential area of application: agro No effect
Reference
VERTEC BIOSOLVENTS, INC.
Patent: WO2006/65935 A2, 2006 ; Title/Abstract Full Text Show Details
59 of 63
Effect (Pharmacological Data)
Phytotoxicity
Species or Test-System (Pharmacological Data)
ryegrass
Method (Pharmacological Data)
Example 3 : Tests for Potential Phytotoxicity of Sprayed Aqueous Solvents; The potential for phytotoxicity (plant injury) by spraying 1 to 2percent aqueous solutions of ethyl lactate and solvent blends with ethyl lactate, as well as other ingredients such as glycerol and soy methyl esters was evaluated in field tests with apple trees and in greenhouse tests with corn, green bean, cucumber, tomato, ryegrass and hosta seedlings. The results showed no evidence of phytotoxicity for any of these solvent blends.In field tests with grapes this GA formulation with the solvent blend showed no adverse effects and gave the same results as to yield and performance as the control that used the standard 4percent GA in IPA formulation. EPO Each of the patents and articles cited herein is incorporated by reference. The use of the article "a" or "an" is intended to include one or more.
Location
Page/Page column 11
Comment (Pharmacological Data)
potential area of application: agro No effect
Reference
VERTEC BIOSOLVENTS, INC.
Patent: WO2006/65935 A2, 2006 ; Title/Abstract Full Text Show Details
60 of 63
Effect (Pharmacological Data)
Phytotoxicity
Species or Test-System (Pharmacological Data)
Hosta
Method (Pharmacological Data)
Example 3 : Tests for Potential Phytotoxicity of Sprayed Aqueous Solvents; The potential for phytotoxicity (plant injury) by spraying 1 to 2percent aqueous solutions of ethyl lactate and solvent blends with ethyl lactate, as well as other ingredients such as glycerol and soy methyl esters was evaluated in field tests with apple trees and in greenhouse tests with corn, green bean, cucumber, tomato, ryegrass and hosta seedlings. The results showed no evidence of phytotoxicity for any of these solvent blends.In field tests with grapes this GA formulation with the solvent blend showed no adverse effects and gave the same results as to yield and performance as the control that used the standard 4percent GA in IPA formulation. EPO Each of the patents and articles cited herein is incorporated by reference. The use of the article "a" or "an" is intended to include one or more.
Location
Page/Page column 11
Comment (Pharmacological Data)
potential area of application: agro No effect
Reference
VERTEC BIOSOLVENTS, INC.
Patent: WO2006/65935 A2, 2006 ; Title/Abstract Full Text Show Details
61 of 63
Effect (Pharmacological Data)
Phytotoxicity
Species or Test-System (Pharmacological Data)
grape
Method (Pharmacological Data)
Example 3 : Tests for Potential Phytotoxicity of Sprayed Aqueous Solvents; The potential for phytotoxicity (plant injury) by spraying 1 to 2percent aqueous solutions of ethyl lactate and solvent blends with ethyl lactate, as well as other ingredients such as glycerol and soy methyl esters was evaluated in field tests with apple trees and in greenhouse tests with corn, green bean, cucumber, tomato, ryegrass and hosta seedlings. The results showed no evidence of phytotoxicity for any of these solvent blends.In field tests with grapes this GA formulation with the solvent blend showed no adverse effects and gave the same results as to yield and performance as the control that used the standard 4percent GA in IPA formulation. EPO Each of the patents and articles cited herein is incorporated by reference. The use of the article "a" or "an" is intended to include one or more.
Location
Page/Page column 11
Comment (Pharmacological Data)
potential area of application: agro No effect
Reference
VERTEC BIOSOLVENTS, INC.
Patent: WO2006/65935 A2, 2006 ; Title/Abstract Full Text Show Details
62 of 63
63 of 63
Effect (Pharmacological Data)
fibril formation
Species or Test-System (Pharmacological Data)
β-amyloid (1-42)
Method (Pharmacological Data)
PBS; room temp.; incubated for 1 h; aggregation of peptide measured by thioflavin fluorescence assay
Comment (Pharmacological Data)
No effect
Reference
Kim, Hee; Park, Byeoung-Soo; Lee, Kwang-Geun; Cheol, Yong Choi; Sung, Sik Jang; Kim, Young-Ho; Lee, Sung-Eun
Journal of Agricultural and Food Chemistry, 2005 , vol. 53, # 22 p. 8537 - 8541 Title/Abstract Full Text View citing articles Show Details
Effect (Pharmacological Data)
antibacterial E. coli ATCC 25922
Species or Test-System (Pharmacological Data) Method (Pharmacological Data)
EXAMPLE 1 [0022] The following example demonstrates that ethyl lactate is a potent bactericide. Using a modification of AOAC Method 956.17, the lower effective concentration for ethyl lactate was tested against E. coli (ATCC 25922) at three reaction times at varying concentrations of ethyl lactate. As the results in Table 1 show, exposure of E. coli to a 15percent solution of ethyl lactate for 10 minutes eliminated bacterial growth.; EXAMPLE 2 [0023] The following example shows one preferred embodiment according to the invention. A formulation is prepared as follows; [0024] Fragrance is added first to the ethyl lactate and then mixed in the water. [0025] Turning to Table 2 there is shown that the bactericidal efficiency of the formulation in Example 2 is comparable to that of 10percent Clorox at the challenge times observed
Results
after treatment with 10-50percent solution of title comp. the bacteria growth observed at 10percent solution in 15 min and at 15percent solution in 5 min (not in 15 min); after treatment with composition containing title comp. at 16 wtpercent the bacteria growth was not observed in 5-15 min
Location
Page 2
Reference
Denton, Robert Michael
Patent: US2005/19355 A1, 2005 ; Title/Abstract Full Text Show Details
Other Data Exposure Assessment (1) 1 of 1
Exposure
waste collection personnel
Sources
garden waste
Reference
Wilkins, Ken; Larsen, Kjeld
Chemosphere, 1996 , vol. 32, # 10 p. 2049 - 2055 Title/Abstract Full Text View citing articles Show Details
Use (277) Use Pattern
Location
Reference
Pharmaceuticals
Page/Page column 7; 11
BEDOUKIAN, Robert H.
Patent: US2015/133406 A1, 2015 ; Title/Abstract Full Text Show Details
control or repellency of biting arthropods
Page/Page column 7; 11
BEDOUKIAN, Robert H.
Patent: US2015/133406 A1, 2015 ; Title/Abstract Full Text Show Details
in combination with one or more alkyl ketones
Page/Page
BEDOUKIAN, Robert H.
column 7; 11
Patent: US2015/133406 A1, 2015 ; Title/Abstract Full Text Show Details
in combination with one or more carboxylic acids
Page/Page column 7; 11
BEDOUKIAN, Robert H.
Patent: US2015/133406 A1, 2015 ; Title/Abstract Full Text Show Details
in combination with one or more of the repellents DEET®, PMD, Picaridin, or other nitrogen containing repellents selected from amines, amides and nitrogen containing heterocyclic compounds
Page/Page column 7; 11
BEDOUKIAN, Robert H.
Patent: US2015/133406 A1, 2015 ; Title/Abstract Full Text Show Details
Agricultural use
Page/Page column 108; 110
OLFACTOR LABORATORIES INCORPORATED; BROWN, Michelle, Ardella; LOMELI, Martin, Antonio, Jr.; ELKASHEF, Samer; ZION, Tricia; FRUTOS, Ulises
Patent: WO2014/28835 A2, 2014 ; Title/Abstract Full Text Show Details
killing a vector pest toward a flying dipteran, bad bugs
Page/Page column 108; 110
OLFACTOR LABORATORIES INCORPORATED; BROWN, Michelle, Ardella; LOMELI, Martin, Antonio, Jr.; ELKASHEF, Samer; ZION, Tricia; FRUTOS, Ulises
Patent: WO2014/28835 A2, 2014 ; Title/Abstract Full Text Show Details
repelling a vector pest
Page/Page column 108; 110
OLFACTOR LABORATORIES INCORPORATED; BROWN, Michelle, Ardella; LOMELI, Martin, Antonio, Jr.; ELKASHEF, Samer; ZION, Tricia; FRUTOS, Ulises
Patent: WO2014/28835 A2, 2014 ; Title/Abstract Full Text Show Details
Pharmaceuticals
topical treatment of warts in composition with formic acid
permeability enhancing agent adapted to increase the permeability of the heavy metal stabilizing agent into the paint layer
Page/Page column 20; 21; 22
ABBEX AB; LICHT, Flemming
Patent: WO2013/180606 A1, 2013 ;
Page/Page column 20; 21; 22
ABBEX AB; LICHT, Flemming
Patent: WO2013/180606 A1, 2013 ;
Title/Abstract Full Text Show Details
Title/Abstract Full Text Show Details
MT2, LLC
Patent: US7314512 B2, 2008 ; Title/Abstract Full Text Show Details
reactive coating composition
MT2, LLC
Patent: US7314512 B2, 2008 ; Title/Abstract Full Text Show Details
part of composition for controlling weeds or grasses
Dow AgroSciences LLC
Patent: US2008/58209 A1, 2008 ; Title/Abstract Full Text Show Details
Skin rejuvenation cream
Ad Lunam Labs, Inc.
Patent: US2008/153757 A1, 2008 ; Title/Abstract Full Text Show Details
Skin moisturizer
Ad Lunam Labs, Inc.
Patent: US2008/153757 A1, 2008 ; Title/Abstract Full Text Show Details
wrinkles
Ad Lunam Labs, Inc.
Patent: US2008/153757 A1, 2008 ; Title/Abstract Full Text Show Details
Skin affected by intrinsic aging
Ad Lunam Labs, Inc.
Patent: US2008/153757 A1, 2008 ; Title/Abstract Full Text Show Details
Photo-induced aging
Ad Lunam Labs, Inc.
Patent: US2008/153757 A1, 2008 ; Title/Abstract Full Text Show Details
Skin cream
Ad Lunam Labs, Inc.
Patent: US2008/153757 A1, 2008 ; Title/Abstract Full Text Show Details
Pain of sunburns
Ad Lunam Labs, Inc.
Patent: US2008/153757 A1, 2008 ; Title/Abstract Full Text Show Details
Use Pattern
Reference
Red skin
Ad Lunam Labs, Inc.
Patent: US2008/153757 A1, 2008 ; Title/Abstract Full Text Show Details
Irritated skin
Ad Lunam Labs, Inc.
Patent: US2008/153757 A1, 2008 ; Title/Abstract Full Text Show Details
Dry skin
Ad Lunam Labs, Inc.
Patent: US2008/153757 A1, 2008 ; Title/Abstract Full Text Show Details
Cracked skin
Ad Lunam Labs, Inc.
Patent: US2008/153757 A1, 2008 ; Title/Abstract Full Text Show Details
Itchy skin
Ad Lunam Labs, Inc.
Patent: US2008/153757 A1, 2008 ; Title/Abstract Full Text Show Details
Atopic dermatitis
Ad Lunam Labs, Inc.
Patent: US2008/153757 A1, 2008 ; Title/Abstract Full Text Show Details
Psoriasis
Ad Lunam Labs, Inc.
Patent: US2008/153757 A1, 2008 ; Title/Abstract Full Text Show Details
Ichthyosis
Ad Lunam Labs, Inc.
Patent: US2008/153757 A1, 2008 ; Title/Abstract Full Text Show Details
Skin lightening
QUEST INTERNATIONAL SERVICES B.V.
Patent: WO2008/113495 A2, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating cancer
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
permeation enhancer in a composition for treating neoplasm
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
permeation enhancer in a composition for treating malignant tumors
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating leukemias
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating lymphomas
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating melanomas
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinomas
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating sarcomas
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating tumor
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating cancer of the brain
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating cancer of the breast
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating cancer of the pancreas
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating cancer of the cervix
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating cancer of the colon
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating cancer of the head and neck
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating cancer of the kidney
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating cancer of the lung
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating cancer of the non-small cell lung
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating melanoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating mesothelioma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating cancer of the ovary
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating cancer of the stomach
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating sarcoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating cancer of the uterus
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating medulloblastoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating chondrosarcoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating fibrosarcoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating lymphosarcoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating melanosarcoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating myxosarcoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating osteosarcoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating adipose sarcoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating liposarcoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating alveolar soft part sarcoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ;
Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating ameloblastic sarcoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating botryoid sarcoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating chloroma sarcoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating chorine carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating embryonal sarcoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating Wilms' tumor sarcoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating endometrial sarcoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating stromal sarcoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating Ewing's sarcoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating fascial sarcoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating fibroblastic sarcoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating giant cell sarcoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating granulocytic sarcoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating Hodgkin's sarcoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating idiopathic multiple pigmented hemorrhagic sarcoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating immunoblastic sarcoma of B cells
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating immunoblastic sarcoma of T-cells
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating Jensen's sarcoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating Kaposi's sarcoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating Kupffer cell sarcoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating angiosarcoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating leukosarcoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating malignant mesenchymoma sarcoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating parosteal sarcoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating reticulocytic sarcoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating Rous sarcoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating serocystic sarcoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating synovial sarcoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating telangiectatic sarcoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating acrallentiginous melanoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating amelanotic melanoma
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Patent: US2008/233183 A1, 2008 ;
Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating benign juvenile I melanoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating Cloudman's melanoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating S91 melanoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating Harding-Passey melanoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating juvenile melanoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating lentigo maligna melanoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating malignant melanoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating nodular melanoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating subungual melanoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating superficial spreading melanoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating acinar carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating acinous carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating adenocystic carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating adenoid cystic carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma adenomatosum
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma of the adrenal cortex
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating alveolar carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating alveolar cell carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating basal cell carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma basocellulare
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating basaloid carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating basosquamous cell carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating bronchioalveolar carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating bronchiolar carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating bronchogenic carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating cerebriform carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating cholangiocellular carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating chorionic carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating colloid carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating comedo carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating corpus carcinoma
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Patent: US2008/233183 A1, 2008 ;
Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating cribriform carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma en cuirasse
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma cutaneum
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating cylindrical carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating cylindrical cell carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating duct carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma durum
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating embryonal carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating encephaloid carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating epiermoid carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma epitheliale adenoides
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating exophytic carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma ex ulcere
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma fibrosum
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating gelatiniform carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating gelatinous carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating giant cell carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma gigantocellulare
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating glandular carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating granulosa cell carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating hair-matrix carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating hematoid carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating hepatocellular carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating Hurthle cell carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating hyaline carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating hypemephroid carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating infantile embryonal carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma in situ
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating intraepidermal carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating intraepithelial carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating Krompecher's carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ;
Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating Kulchitzky-cell carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating large-cell carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating lenticular carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma lenticulare
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating lipomatous carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating lymphoepithelial carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma medullare
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating medullary carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating melanotic carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma moue
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating mucinous carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma muciparum
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma mucocellulare
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating mucoepidermoid carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma mucosum
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating mucous carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma myxomatodes
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating nasopharyngeal carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating oat cell carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma ossificans
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating osteoid carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating papillary carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating periportal carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating preinvasive carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating prickle cell carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating pultaceous carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating renal cell carcinoma of kidney
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating reserve cell carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma sarcomatodes
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating schneiderian carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating scirrhous carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ;
Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma scroti
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating signet-ring cell carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma simplex
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating small-cell carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating solenoid carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating spheroidal cell carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating spindle cell carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma spongiosum
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating squamous carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating squamous cell carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating string carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma telangiectaticum
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating carcinoma telangiectodes
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating transitional cell carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhacer in a composition for treating carcinoma tuberosum
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating tuberous carcinoma
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating verrucous carcinoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating Hodgkin's Disease
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating Non-Hodgkin's Lymphoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating multiple myeloma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating neuroblastoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating rhabdomyosarcoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating primary thrombocytosis
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating primary macroglobulinemia
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating small-cell lung tumors
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating primary brain tumors
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating malignant pancreatic insulanoma
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating malignant carcinoid
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating premalignant skin lesions
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating testicular cancer
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating thyroid cancer
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ;
Title/Abstract Full Text Show Details
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ;
Permeation enhancer in a composition for treating esophageal cancer
Title/Abstract Full Text Show Details
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ;
Permeation enhancer in a composition for treating genitourinary tract cancer
Title/Abstract Full Text Show Details
Use Pattern Permeation enhancer in a composition for treating malignant hypercalcemia
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Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating endometrial cancer
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating adrenal cortical cancer
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
Permeation enhancer in a composition for treating prostate cancer
PATHFINDER MANAGEMENT, INC.
Patent: US2008/233183 A1, 2008 ; Title/Abstract Full Text Show Details
dry seborrhoea
CARDON PHAMACEUTICALS NV
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ingredient of a composition suitable for the treatment of animals
CARDON PHAMACEUTICALS NV
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Solvent for pesticidal formulations
LIVIE BIOPESTICIDES LIMITED
Patent: WO2008/35029 A2, 2008 ; Title/Abstract Full Text Show Details
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Patent: WO2008/35029 A2, 2008 ; Title/Abstract Full Text Show Details
Solvent for acaricidal compositions
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Patent: WO2008/35029 A2, 2008 ; Title/Abstract Full Text Show Details
Solvent for agricultural compositions
VALENT BIOSCIENCES CORPORATION
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Solvent for agrochemical formulations
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Patent: WO2008/143969 A1, 2008 ; Title/Abstract Full Text Show Details
VALENT BIOSCIENCES CORPORATION
Patent: WO2008/143990 A1, 2008 ; Title/Abstract Full Text Show Details
Hydroxylic matrix forming agent for a stripless depilatory composition
BIODERM RESEARCH
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Title/Abstract Full Text Show Details
Lin, Samuel Qcheng Sun
Patent: US2007/71703 A1, 2007 ;
polar activator in master gel composition
Title/Abstract Full Text Show Details
SYGENTA PARTICIPATIONS AG
Patent: WO2007/73933 A2, 2007 ;
Component of herbicidal composition useful for improving stability of active agent
Title/Abstract Full Text Show Details
Component for preparation of dinotefuran insecticidal formulations
Page/Page column 4-5; 7-8; 12-13
Cottrell, Ian W.; Ahn, Albert; Dorneval, Linda
Patent: US2007/254951 A1, 2007 ; Title/Abstract Full Text Show Details
Cleaning agent
Arkema,
Patent: US2006/41165 A1, 2006 ; Title/Abstract Full Text Show Details
Degreasing agent
Arkema,
Patent: US2006/41165 A1, 2006 ; Title/Abstract Full Text Show Details
Defluxing of printed circuits
Arkema,
Patent: US2006/41165 A1, 2006 ; Title/Abstract Full Text Show Details
Temporary protection for solid surfaces, such as metal components, creamics, glass or plastics
Arkema,
Patent: US2006/41165 A1, 2006 ; Title/Abstract Full Text Show Details
composition for administering a cyclosporin compound
Dexcel Ltd.
Patent: US7026290 B1, 2006 ; Title/Abstract Full Text Show Details
amphiphilic solvent
Dexcel Ltd.
Patent: US7026290 B1, 2006 ; Title/Abstract Full Text Show Details
pharmaceutical suspension
ALZA CORPORATION
Patent: WO2006/83799 A2, 2006 ; Title/Abstract Full Text Show Details
suspending vehicle
ALZA CORPORATION
Patent: WO2006/83799 A2, 2006 ; Title/Abstract Full Text Show Details
Solvent
LIVIE BIOPESTICIDES LIMITED; NATIONAL RESEARCH DEVELOPMENT CORPORATION
Patent: WO2006/111692 A1, 2006 ; Title/Abstract Full Text Show Details
flowable composition comprising a biodegradable thermoplastic polymer for sustained delivery of octreotide compounds
QLT USA, INC.; WARREN, Stephen, L.; DADEY, Eric; DUNN, Richard, L.; DOWNING, John, Milton; LI, Ellen, Qi
Patent: WO2006/65951 A2, 2006 ; Title/Abstract Full Text Show Details
biocompatible polar aprotic liquid
QLT USA, INC.; WARREN, Stephen, L.; DADEY, Eric; DUNN, Richard, L.; DOWNING, John, Milton; LI, Ellen, Qi
Patent: WO2006/65951 A2, 2006 ; Title/Abstract Full Text Show Details
skin penetration enhancing agent for the composition
BIODERM RESEARCH
Patent: US2006/110415 A1, 2006 ;
Title/Abstract Full Text Show Details
Second anesthetic for anesthetic composition
DURECT CORPORATION
Patent: WO2006/33948 A2, 2006 ; Title/Abstract Full Text Show Details
Solvent for anesthetic composition
DURECT CORPORATION
Patent: WO2006/33948 A2, 2006 ; Title/Abstract Full Text Show Details
Biocompatible, water-miscible solvent of a polymer-based injectable gel-forming composition for intratissue implantation
ASSISTANCE PUBLIQUE-HOPITAUX DE PARIS; UNIVERSITE PARIS SUD XI
Patent: US2006/210635 A1, 2006 ; Title/Abstract Full Text Show Details
Biocompatible, water-miscible solvent of a polymer-based injectable gel-forming composition for intravascular implantation
ASSISTANCE PUBLIQUE-HOPITAUX DE PARIS; UNIVERSITE PARIS SUD XI
Patent: US2006/210635 A1, 2006 ; Title/Abstract Full Text Show Details
Biocompatible, water-miscible solvent of a of a polymer-based injectable gel-forming composition for filling cavities
ASSISTANCE PUBLIQUE-HOPITAUX DE PARIS; UNIVERSITE PARIS SUD XI
Patent: US2006/210635 A1, 2006 ; Title/Abstract Full Text Show Details
Biocompatible, water-miscible solvent of a polymer-based injectable gel-forming composition for producing therapeutic vascular occlusions
ASSISTANCE PUBLIQUE-HOPITAUX DE PARIS; UNIVERSITE PARIS SUD XI
Patent: US2006/210635 A1, 2006 ; Title/Abstract Full Text Show Details
Biocompatible, water-miscible solvent of a polymer-based injectable gel-forming composition for tissue reconstruction
ASSISTANCE PUBLIQUE-HOPITAUX DE PARIS; UNIVERSITE PARIS SUD XI
Patent: US2006/210635 A1, 2006 ; Title/Abstract Full Text Show Details
Biocompatible, water-miscible solvent of a polymer-based injectable gel-forming composition for the treatment of gastro-esophageal reflux
ASSISTANCE PUBLIQUE-HOPITAUX DE PARIS; UNIVERSITE PARIS SUD XI
Patent: US2006/210635 A1, 2006 ; Title/Abstract Full Text Show Details
Biocompatible, water-miscible solvent of a polymer-based injectable gel-forming composition for the treatment of urinary incontinence
ASSISTANCE PUBLIQUE-HOPITAUX DE PARIS; UNIVERSITE PARIS SUD XI
Patent: US2006/210635 A1, 2006 ; Title/Abstract Full Text Show Details
Biocompatible, water-miscible solvent of a polymer-based injectable gel-forming composition for percutaneous implantation
ASSISTANCE PUBLIQUE-HOPITAUX DE PARIS; UNIVERSITE PARIS SUD XI
Patent: US2006/210635 A1, 2006 ; Title/Abstract Full Text Show Details
Biocompatible, water-miscible solvent of a polymer-based injectable gel-forming composition for reducing wrinkle
ASSISTANCE PUBLIQUE-HOPITAUX DE PARIS; UNIVERSITE PARIS SUD XI
Patent: US2006/210635 A1, 2006 ; Title/Abstract Full Text Show Details
Biocompatible, water-miscible solvent of a polymer-based injectable gel-forming composition for filling pipes
ASSISTANCE PUBLIQUE-HOPITAUX DE PARIS; UNIVERSITE PARIS SUD XI
Patent: US2006/210635 A1, 2006 ; Title/Abstract Full Text Show Details
organic solvent for a dispersed phase formulation containing a gonadotropin releasing hormone antagonist
OAKWOOD LABORATORIES, L.L.C
Patent: WO2006/10155 A2, 2006 ; Title/Abstract Full Text Show Details
Solvent for formulations of plant growth regulators (PGRs)
VERTEC BIOSOLVENTS, INC.
Patent: WO2006/65935 A2, 2006 ; Title/Abstract Full Text Show Details
liquid plant growth promoter concentrate composition
VERTEC BIOSOLVENTS, INC.
Patent: WO2006/65935 A2, 2006 ; Title/Abstract Full Text Show Details
active component composition for desinfection skin
Denton, Robert Michael
Patent: US2005/19355 A1, 2005 ; Title/Abstract Full Text Show Details
fungicide
Denton, Robert Michael
Patent: US2005/20678 A1, 2005 ; Title/Abstract Full Text Show Details
water immiscible solvent of injectable composition for the administration of a pharmacologically active compound
IDEXX Laboratories, Inc.
Patent: US2005/49210 A1, 2005 ; Title/Abstract Full Text Show Details
pharmaceutically acceptable solvent for immunogenic composition
INSTITUT PASTEUR; CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS)
Patent: EP1529536 A1, 2005 ; Title/Abstract Full Text Show Details
water miscible solvent - component of pharmaceutical composition for skin treatment
ALPHARX INC.
Patent: US2005/255133 A1, 2005 ; Title/Abstract Full Text Show Details
pharmaceutical composition
Muse, Joel; Colvin, Howard A.
Patent: US2005/287179 A1, 2005 ; Title/Abstract Full Text Show Details
dispersing excipient
Muse, Joel; Colvin, Howard A.
Patent: US2005/287179 A1, 2005 ; Title/Abstract Full Text Show Details
emulsifying excipient
Muse, Joel; Colvin, Howard A.
Patent: US2005/287179 A1, 2005 ; Title/Abstract Full Text Show Details
Pharmaceutical formulation
Murthy, Yerramilli V. S. N.
Patent: US2005/287219 A1, 2005 ; Title/Abstract Full Text Show Details
Organic solvent
Murthy, Yerramilli V. S. N.
Patent: US2005/287219 A1, 2005 ; Title/Abstract Full Text Show Details
dermatologically-compatible solvent for dry cow udder protection composition
KROSS, Robert, D.
Patent: WO2005/94787 A1, 2005 ; Title/Abstract Full Text Show Details
viscosity-reducing agent for more effective plasticizing effect
Serpelloni, Michel; Mentink, Leon; Bernaerts, Joel
Patent: US2005/58712 A1, 2005 ; Title/Abstract Full Text Show Details
biocompatibile solvent for high viscosity embolizing composition
Greff, Richard J.
Patent: US2003/228273 A1, 2003 ; Title/Abstract Full Text Show Details
embolization of blood vessels
Greff, Richard J.
Patent: US2003/228273 A1, 2003 ; Title/Abstract Full Text Show Details
treatment of aneurysms
Greff, Richard J.
Patent: US2003/228273 A1, 2003 ; Title/Abstract Full Text Show Details
Isolation from Natural Product (2) Isolation from Natural Product
Reference
Abbau v. Rohrzucker
Ito
Agricultural and Biological Chemistry, 1977 , vol. 41, # 7 p. 1307 - 1308 Title/Abstract Full Text View citing articles Show Details
In Ananasfruechten
Connell
Australian Journal of Chemistry, 1964 , vol. 17, p. 130,131 Full Text Show Details
Quantum Chemical Calculations (2) Calculated Properties
Method (Quantum Chemical Calculations)
Location
Reference
IR bands, intensities, transition moments
Ab initio calcns. (LCAO, GO SCF, DIM, SAMO, X-à, Hartree-Fock)
supporting information
Garca, Gregorio; Aparicio, Santiago; Atilhan, Mert
Journal of Molecular Liquids, 2014 , vol. 199, p. 215 - 223 Title/Abstract Full Text View citing articles Show Details
IR bands, intensities, transition moments
Ab initio calcns. (LCAO, GO SCF, DIM, SAMO, X-à, Hartree-Fock)
Tsui, Hung-Wei; Wang, N.-H. Linda; Franses, Elias I.
Journal of Physical Chemistry B, 2013 , vol. 117, # 31 p. 9203 - 9216 Title/Abstract Full Text View citing articles Show Details