JPS5659796A - Purification of ursodeoxycholic acid or chenodeoxycholic acid - Google Patents

Purification of ursodeoxycholic acid or chenodeoxycholic acid

Info

Publication number
JPS5659796A
JPS5659796A JP13574379A JP13574379A JPS5659796A JP S5659796 A JPS5659796 A JP S5659796A JP 13574379 A JP13574379 A JP 13574379A JP 13574379 A JP13574379 A JP 13574379A JP S5659796 A JPS5659796 A JP S5659796A
Authority
JP
Japan
Prior art keywords
acid
column
ursodeoxycholic
eluent
chenodeoxycholic
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP13574379A
Other languages
Japanese (ja)
Inventor
Fumio Kamiyama
Kazutoshi Yamazaki
Takashi Kamata
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sekisui Chemical Co Ltd
Original Assignee
Sekisui Chemical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sekisui Chemical Co Ltd filed Critical Sekisui Chemical Co Ltd
Priority to JP13574379A priority Critical patent/JPS5659796A/en
Publication of JPS5659796A publication Critical patent/JPS5659796A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE: The titled compound that is used as a remedy for cholelithiasis is purified through a liquid chromatography where the porous particles of styrenedivinylbenzene copolymer is used as the stationary phase and a solvent with a specific solubility parameter is used as an eluent with industrial advantage.
CONSTITUTION: A crude product including ursodeoxycholic acid, chenodeoxychlolic acid, cholic acid, lithocholic acid, etc., is dissolved in methanol or the like to prepare the sample solution. Then, a column filled with porous particles of styrene- divinylbenzene copolymer as the stationary phase is connected to a liquid chromatography and a solvent with a solubility parameter of 11W17 such as methanol is passed through the column as an eluent. The sample solution is added to the column and eluted to give a chromatogram of ursodeoxycholic acid (1) and chenodeoxycholic acid (2) and they are obtained in pure form.
COPYRIGHT: (C)1981,JPO&Japio
JP13574379A 1979-10-19 1979-10-19 Purification of ursodeoxycholic acid or chenodeoxycholic acid Pending JPS5659796A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13574379A JPS5659796A (en) 1979-10-19 1979-10-19 Purification of ursodeoxycholic acid or chenodeoxycholic acid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13574379A JPS5659796A (en) 1979-10-19 1979-10-19 Purification of ursodeoxycholic acid or chenodeoxycholic acid

Publications (1)

Publication Number Publication Date
JPS5659796A true JPS5659796A (en) 1981-05-23

Family

ID=15158826

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13574379A Pending JPS5659796A (en) 1979-10-19 1979-10-19 Purification of ursodeoxycholic acid or chenodeoxycholic acid

Country Status (1)

Country Link
JP (1) JPS5659796A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008069152A (en) * 2006-09-12 2008-03-27 Dipharma Francis Srl Process for preparing cholanic acid
KR100997675B1 (en) 2008-12-30 2010-12-01 (주)파마피아 Method for manufacturing magnesium salt of chenodeoxycholic acid and ursodeoxycholic acid
CN103852554A (en) * 2012-11-30 2014-06-11 山东阿如拉药物研究开发有限公司 Quality detection method for Tibetan medicinal composition oxytropis itch-relieving preparation

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008069152A (en) * 2006-09-12 2008-03-27 Dipharma Francis Srl Process for preparing cholanic acid
KR100997675B1 (en) 2008-12-30 2010-12-01 (주)파마피아 Method for manufacturing magnesium salt of chenodeoxycholic acid and ursodeoxycholic acid
CN103852554A (en) * 2012-11-30 2014-06-11 山东阿如拉药物研究开发有限公司 Quality detection method for Tibetan medicinal composition oxytropis itch-relieving preparation
CN103852554B (en) * 2012-11-30 2015-11-18 山东金诃药物研究开发有限公司 A kind of Tibetan medicinal composition whin disappears the quality determining method of preparation of itching

Similar Documents

Publication Publication Date Title
US7235540B2 (en) Methods of using 2-methoxyestradiol of high purity
Ikekawa et al. Separation of vitamin D3 metabolites and their analogues by high-pressure liquid chromatography
JPS5659796A (en) Purification of ursodeoxycholic acid or chenodeoxycholic acid
Danielsson Reversed phase partition chromatography of some C27-steroids Bile acids and steroids 38
JP2012211132A (en) Method of preparing 2-methoxyestradiol of high purity
Schneider et al. 1β-Hydroxylation of 3α, 17α, 20β, 21-tetrahydroxy-5β-pregnan-11-one and of other 5β-steroids in a man and by surviving liver slices of the guinea pig
JPS56117781A (en) Preparation of sweetening matter
JPS57145899A (en) Steroid saponin and its preparation
Iida et al. High-performance liquid chromatographic behavior of 2-, 4-and 6-hydroxylated bile acid stereoisomers
JPS5244142A (en) Differential amplifier
Hammond et al. The gas chromatography of human steroids as the trimethylsilyl ethers
Bull et al. High-performance liquid chromatography of bile pigments: Separation and characterization of the urobilinoids
JPS6259116B2 (en)
JPS5227741A (en) Method of preparing schiff-base liquid crystals of high purity and app aratus for the same
MATSUMOTO et al. CHROMATOGRAPHIC SEPARATION OF C21O2-STEROIDS AND PREGNANE-3α, 17α, 20α-TRIOL ON THE COLUMN OF PARTIALLY ESTERIFIED CARBOXYLIC ACID TYPE ION EXCHANGE RESIN
Batta et al. Chromatographic separation of putative precursors of cholestanol
Albrecht et al. Improved procedures for the preparation of 2, 4-dibromoestriol and dideuterioestriol
AU2005211579B8 (en) Compositions comprising purified 2-methoxyestradiol and methods of producing same
JPS5283443A (en) Separation of naphthoquinone
JPS565095A (en) Purification of kallidinogenase
GB1133903A (en) Process for obtaining tocopherols
JPS57128646A (en) 7-hydroxylabda-8(20),12,14-triene and agent for improving taste and flavor of tobacco composed of said compound
JPS5271500A (en) Purification of colesterol
JPS5630941A (en) Purification of coenzyme q
Touchstone et al. Isolation of cortisol from the brain of the rhesus monkey