Chenodeoxycholic acid 474-25-9 large in supply CAS NO.474-25-9

Synonyms: URSODEOXYCHOLOC ACID;3,7-dihydroxy-,(3-alpha,5-beta,7-alpha)-cholan-24-oicaci;3,7-dihydroxy-,(3alpha,5beta,7alpha)-cholan-24-oicaci;3,7-Dihydroxy-5-Cholanicacid;3-alpha,7-alpha-dihydroxy-5-beta-cholan-24-oicaci;3-alpha,7-alpha-dihydroxy-5-beta-cholan-24-oicacid;3-alpha,7-alpha-dihydroxycholanicacid;3-alpha,7-alpha-dihydroxycholansaeure
CAS: 474-25-9
MF: C24H40O4
MW: 392.57
EINECS: 207-481-8
Product Categories: Intermediates & Fine Chemicals;Pharmaceuticals;Steroids;Intracellular receptor;Inhibitors
Mol File: 474-25-9.mol
Chenodeoxycholic acid Structure
Chenodeoxycholic acid Chemical Properties
Melting point  165-167 °C(lit.)
alpha  12 º (c=1, CHCl3)
storage temp.  Refrigerator
solubility  PRACTICALLY INSOLUBLE
Water Solubility  PRACTICALLY INSOLUBLE
Merck  13,2062
CAS DataBase Reference 474-25-9(CAS DataBase Reference)
EPA Substance Registry System Cholan-24-oic acid, 3,7-dihydroxy-, (3.alpha.,5.beta.,7.alpha.)- (474-25-9)
Safety Information
Hazard Codes  Xn
Risk Statements  63
Safety Statements  22-24/25-45-36/37
WGK Germany  2
RTECS  FZ1980000

Chenodeoxycholic acid Chemical Properties

mp  165-167 °C(lit.)

alpha  12 º (c=1, CHCl3)
storage temp.  Refrigerator
solubility  PRACTICALLY INSOLUBLE
Water Solubility  PRACTICALLY INSOLUBLE
Merck  13,2062
CAS DataBase Reference 474-25-9(CAS DataBase Reference)
EPA Substance Registry System Cholan-24-oic acid, 3,7-dihydroxy-, (3.alpha.,5.beta.,7.alpha.)- (474-25-9)

Safety Information

Hazard Codes  Xn
Risk Statements  63
Safety Statements  22-24/25-45-36/37
WGK Germany  2

RTECS  FZ1980000

Chenodeoxycholic acid Usage And Synthesis

Chemical Properties Off-White Solid
Usage vitamin D3
Usage anticholithogenic, antilipemic agent
Usage A major bile acid in many vertebrates, occurring as the N-glycine and/or N-taurine conjugate. With other bile acids, forms mixed micelles with lecithin in bile which solubilize cholesterol and thus fa cilitates its excretion. Fcilitates fat absorption in the small intestine by micellar solubilization of fatty acids and monoglycerides. Anticholelithogenic. Epimeric with Ursodiol.

Chenodeoxycholic acid Preparation Products And Raw materials

Preparation Products Ursodeoxycholic acid-->squalamine
Raw materials Etanol-->Sodium carbonate-->Barium chloride-->Hydrochloric acid alcohol-->Sodium cholate