US2003141252A1PendingUtilityA1
Separating agent for optical isomer
Priority: Mar 7, 2001Filed: Mar 7, 2002Published: Jul 31, 2003
Est. expiryMar 7, 2021(expired)· nominal 20-yr term from priority
B01J 20/285B01J 20/29C07H 13/02C07B 57/00B01J 20/281B01J 20/22B01J 20/24B01J 2220/54B01J 20/262B01D 15/3833B01J 20/265
42
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Claims
Abstract
The present invention provides a separating agent for enantiomeric isomers having no large UV absorption as represented by an aromatic group and having high asymmetric recognizability, particularly, high asymmetric recognizability in an aqueous mobile phase, or a separating agent for enantiomeric isomers comprising a polysaccharide alicyclic ester derivative free from aromatic group as an effective component.
Claims
exact text as granted — not AI-modified1 . A separating agent for enantiomeric isomers comprising a polysaccharide alicyclic ester derivative free from aromatic group as an effective component.
2 . The separating agent for enantiomeric isomers according to claim 1 wherein the polysaccharide alicyclic ester derivative is a cellulose derivative.
3 . The separating agent for enantiomeric isomers according to one of claims 1 and 2 wherein the alicyclic ester derivative is a cycloalkylcarboxylate derivative.
4 . The separating agent for enantiomeric isomers according to any one of claims 1 to 3 , which is used as a chiral stationary phase for chromatography.
5 . The separating agent for enantiomeric isomers according to claim 4 wherein the chiral stationary phase for chromatography is a chiral stationary phase for liquid chromatography used under a reversed phase condition.
6 . The separating agent for enantiomeric isomers according to claim 5 wherein the reversed phase condition is a condition having a mobile phase consisting of water, alcohol or acetonitrile alone or a mixture containing a plurality of liquids selected therefrom.
7 . The separating agent for enantiomeric isomers according to claim 4 wherein the chiral stationary phase for chromatography is a stationary phase for thin-layer chromatography.
8 . The separating agent for enantiomeric isomers according to claim 4 wherein the chiral stationary phase for chromatography is an asymmetry recognition agent added to a migrating liquid of capillary electrophoresis or filled in a capillary.
9 . The separating agent for enantiomeric isomers according to claim 4 wherein the chiral stationary phase for chromatography is a stationary phase for continuous liquid preparative chromatography.
10 . The separating agent for enantiomeric isomers according to claim 1 wherein the polysaccharide alicyclic ester derivative is cellulose tris(cyclohexylcarboxylate).
11 . The separating agent for enantiomeric isomers according to claim 1 wherein the polysaccharide alicyclic ester derivative is cellulose tris(cyclopentylcarboxylate) or cellulose tris(cycloadamantylcarboxylate).
12 . A method for separating enantiomeric isomers by a chromatography having a chiral stationary phase containing a polysaccharide alicyclic ester derivative free from aromatic group as an effective component.
13 . The method according to claim 12 wherein the polysaccharide alicyclic ester derivative is cellulose tris(cyclopentylcarboxylate) or cellulose tris(cycloadamantylcarboxylate).Cited by (0)
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