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CAS

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21066-18-2

(3a,5b,6a,12a)-3,6,12-trihydroxy-Cholan-24-oic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 21066-18-2 Structure

  • Basic information

    1. Product Name: (3a,5b,6a,12a)-3,6,12-trihydroxy-Cholan-24-oic acid
    2. Synonyms: (3a,5b,6a,12a)-3,6,12-trihydroxy-Cholan-24-oic acid;6a,12a-Dihydroxylithocholic acid;3,6,12-trihydroxycholanoic acid
    3. CAS NO:21066-18-2
    4. Molecular Formula: C24H40O5
    5. Molecular Weight: 408.57
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 21066-18-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 583.9°C at 760 mmHg
    3. Flash Point: 321°C
    4. Appearance: /
    5. Density: 1.184g/cm3
    6. Vapor Pressure: 4.59E-16mmHg at 25°C
    7. Refractive Index: 1.558
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (3a,5b,6a,12a)-3,6,12-trihydroxy-Cholan-24-oic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3a,5b,6a,12a)-3,6,12-trihydroxy-Cholan-24-oic acid(21066-18-2)
    12. EPA Substance Registry System: (3a,5b,6a,12a)-3,6,12-trihydroxy-Cholan-24-oic acid(21066-18-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 21066-18-2(Hazardous Substances Data)

21066-18-2 Usage

General Description

"(3a,5b,6a,12a)-3,6,12-trihydroxy-Cholan-24-oic acid" is a chemical compound that belongs to the class of cholic acids, which are important components of bile. This specific compound has a steroid structure and contains three hydroxyl (OH) groups at the 3, 6, and 12 positions on the molecule. It is an important component in the digestion and absorption of fats in the body, as bile acids help to emulsify lipids and aid in their absorption in the intestines. Additionally, cholic acids play a role in the regulation of cholesterol and lipid metabolism. This specific compound, with its unique hydroxyl arrangement, likely plays a crucial role in these physiological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 21066-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,6 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21066-18:
(7*2)+(6*1)+(5*0)+(4*6)+(3*6)+(2*1)+(1*8)=72
72 % 10 = 2
So 21066-18-2 is a valid CAS Registry Number.
InChI:InChI=1/C24H40O5/c1-13(4-7-22(28)29)16-5-6-17-15-11-20(26)19-10-14(25)8-9-23(19,2)18(15)12-21(27)24(16,17)3/h13-21,25-27H,4-12H2,1-3H3,(H,28,29)/t13-,14-,15+,16-,17+,18+,19+,20+,21+,23-,24-/m1/s1

21066-18-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name HDCA

1.2 Other means of identification

Product number -
Other names 3α,6α,12α-Trihydroxy-5β-cholan-24-saeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:21066-18-2 SDS

21066-18-2Downstream Products

21066-18-2Relevant articles and documents

Synthesis method of 3[alpha],6[alpha](beta),12[alpha]-trihydroxyl-5[beta]-cholic acid

-

, (2020/10/14)

The invention discloses a preparation method of 3[alpha],6[alpha],12[alpha]-trihydroxyl-5[beta]-cholic acid and 3[alpha],6[beta],12[alpha]-trihydroxyl-5[beta]-cholic acid. 3[alpha],7[alpha],12[alpha]-trihydroxyl-5[beta]-cholic acid is taken as a raw material, and 3[alpha],6[alpha],12[alpha]-trihydroxyl-5[beta]-cholic acid and 3[alpha],6[beta],12[alpha]-trihydroxyl-5[beta]-cholic acid are obtainedthrough ten steps such as Mukaiyama aldol condensation reaction, oxidative cracking, reduction removal and the like . The synthesis method has the characteristics of green and high efficiency.

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