epi-Coprostanol

Base Information

Chemical Name:epi-Coprostanol
CAS No.:516-92-7
Molecular Formula:C27H48 O
Molecular Weight:388.678
Hs Code.:2906130000
NSC Number:18182
UNII:UFH3K1F9EG
DSSTox Substance ID:DTXSID7046700
Nikkaji Number:J39.847K
Wikidata:Q27291059
Metabolomics Workbench ID:36782
ChEMBL ID:CHEMBL1998721
Mol file:516-92-7.mol

Synonyms:3-alpha-hydroxy-5beta-cholestanol;epicoprostanol

Suppliers and Price of epi-Coprostanol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
Epicoprostanol
500mg
$ 500.00

Sigma-Aldrich
5β-Cholestan-3α-ol ≥95%
1g
$ 1040.00

Sigma-Aldrich
5β-Cholestan-3α-ol ≥95%
500mg
$ 535.00

Medical Isotopes, Inc.
5β-Cholestan-3α-ol
25 mg
$ 580.00

American Custom Chemicals Corporation
5BETA-CHOLESTAN-3ALPHA-OL 95.00%
1G
$ 704.49

AHH
5betaCholestan-3alpha-ol 95%
1g
$ 525.00

Total 12 raw suppliers

Chemical Property of epi-Coprostanol

Chemical Property:

Vapor Pressure:3.26E-10mmHg at 25°C
Boiling Point:455.5°Cat760mmHg
Flash Point:190.7°C
PSA：20.23000
Density:0.956g/cm³
LogP:7.46860
Storage Temp.:2-8°C
XLogP3:9.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:388.370516150
Heavy Atom Count:28
Complexity:540

Purity/Quality:

98%,99%, ^*data from raw suppliers

Epicoprostanol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)CCCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C
Isomeric SMILES:C[C@H](CCCC(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC[C@H]4[C@@]3(CC[C@H](C4)O)C)C
Uses 5β-Cholestan-3α-ol was used as internal standard for analysis of sterols in plasma by GC and HPLC.

Technology Process of epi-Coprostanol

There total 68 articles about epi-Coprostanol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

: 111222-20-9
2-[(3S,5R,8R,9S,10S,13R,14S,17R)-17-((R)-1,5-Dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yloxy]-tetrahydro-furan

: 80-97-7,360-68-9,516-92-7,516-95-0,566-84-7,14615-12-4,16720-60-8,17608-41-2,18769-46-5,27409-41-2,56193-35-2,57759-49-6,73465-18-6,103365-91-9,105119-51-5
Coprostanol

Guidance literature:: With toluene-4-sulfonic acid; In ethanol; for 1h; Ambient temperature;
DOI:10.1055/s-1987-27903

Reference yield: 97.0%

: 4-[(3S,5R,8R,9S,10S,13R,14S,17R)-17-((R)-1,5-Dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yloxymethyl]-benzonitrile

: 80-97-7,360-68-9,516-92-7,516-95-0,566-84-7,14615-12-4,16720-60-8,17608-41-2,18769-46-5,27409-41-2,56193-35-2,57759-49-6,73465-18-6,103365-91-9,105119-51-5
Coprostanol

Guidance literature:: With Triethylgermyl-natrium; In 1,4-dioxane; N,N,N,N,N,N-hexamethylphosphoric triamide; at 50 ℃; for 15h;
DOI:10.1246/cl.2002.1032