3alpha,7alpha-dihydroxy-12-oxo-5beta-cholan-24-oic acid
- Product Name
- 3alpha,7alpha-dihydroxy-12-oxo-5beta-cholan-24-oic acid
- CAS No.
- 2458-08-4
- Chemical Name
- 3alpha,7alpha-dihydroxy-12-oxo-5beta-cholan-24-oic acid
- Synonyms
- Einecs 219-542-6;12-Oxocholic acid;Ursodiol Impurity;Cholic Acid Impurity 16;1,3-dimethyl-38-nitrosourea;12-Ketochenodeoxycholic acid;Ursodeoxycholic Acid Impurity 23;Chenodeoxycholic Acid Impurity 10;3,7-Dihydroxy-12-oxocholanoic acid;3α,7α-Dihydroxy-12-oxocholanic acid
- CBNumber
- CB6890359
- Molecular Formula
- C24H38O5
- Formula Weight
- 406.56
- MOL File
- 2458-08-4.mol
3alpha,7alpha-dihydroxy-12-oxo-5beta-cholan-24-oic acid Property
- Boiling point:
- 583℃[at 101 325 Pa]
- Density
- 1.18[at 20℃]
- vapor pressure
- 0Pa at 20℃
- storage temp.
- -20°C
- solubility
- Chloroform: Slightly Soluble
Methanol: Slightly Soluble - pka
- 5[at 20 ℃]
- form
- Solid
- color
- White to off-white
- Water Solubility
- 4.698mg/L at 25℃
- LogP
- 2.97 at 20℃
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
- Precautionary statements
-
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P321Specific treatment (see … on this label).
P332+P313IF SKIN irritation occurs: Get medical advice/attention.
P362Take off contaminated clothing and wash before reuse.
N-Bromosuccinimide Price
- Product number
- SHG0020695
- Product name
- KETOCHOLANIC ACID
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $459.63
- Updated
- 2021/12/16
3alpha,7alpha-dihydroxy-12-oxo-5beta-cholan-24-oic acid Chemical Properties,Usage,Production
Uses
12-Ketochenodeoxycholic acid 12 is a direct precursor of cholodeoxycholic acid (CDCA). Cholodeoxycholic acid is used to cholesterol gallstones and has chemotherapeutic properties that dissolve gallstones[1].
Definition
ChEBI: 3alpha,7alpha-dihydroxy-12-oxo-5beta-cholanic acid is an oxo-5beta-cholanic acid. It is a conjugate acid of a 3alpha,7alpha-dihydroxy-12-oxo-5beta-cholanate.
Flammability and Explosibility
Non flammable
References
[1] Sawada, H. et al. Microbial production of chenodeoxycholic acid precursor, 12-ketochenodeoxycholic acid, from dehydrocholic acid. European Journal of Applied Microbiology and Biotechnology, 10(1–2), 107–112.
[2] J D SUTHERLAND T P F I A Macdonald. The enzymic and chemical synthesis of ursodeoxycholic and chenodeoxycholic acid from cholic acid.[J]. Preparative biochemistry, 1982, 12 4: 307-321. DOI: 10.1080/00327488208065679
[3] A. HOFMANN. The Preparation of Chenodeoxycholic Acid and Its Glycine and Taurine Conjugates.[J]. Acta chemica Scandinavica, 1963, 177 1: 173-186. DOI: 10.3891/acta.chem.scand.17-0173
[4] AIHUA ZHAO. Increased levels of conjugated bile acids are associated with human bile reflux gastritis.[J]. Scientific Reports, 2020: 11601. DOI: 10.1038/s41598-020-68393-5
[5] YIZHONG WANG. Altered gut microbiota and microbial metabolism in children with hepatic glycogen storage disease: a case-control study.[J]. Translational pediatrics, 2023, 12 4: 572-586. DOI: 10.21037/tp-22-293
[6] MOMIR MIKOV. 3Alpha,7alpha-dihydroxy-12-oxo-5beta-cholanate as blood-brain barrier permeator.[J]. Polish journal of pharmacology, 2004, 56 3: 367-371.
[7] MIHALJ POSA. Effect of cholic acid and its keto derivatives on the analgesic action of lidocaine and associated biochemical parameters in rats.[J]. European Journal of Drug Metabolism and Pharmacokinetics, 2007, 32 2: 109-117. DOI: 10.1007/bf03190999
3alpha,7alpha-dihydroxy-12-oxo-5beta-cholan-24-oic acid Preparation Products And Raw materials
Raw materials
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