Androsterone glucuronide

Base Information

Chemical Name:Androsterone glucuronide
CAS No.:1852-43-3
Molecular Formula:C25H38 O8
Molecular Weight:466.572
Hs Code.:
UNII:IMD4XD0W3U
DSSTox Substance ID:DTXSID80862764
Nikkaji Number:J448.218B
Wikipedia:Androsterone_glucuronide
Wikidata:Q27103919
NCI Thesaurus Code:C120007
Metabolomics Workbench ID:36911
Mol file:1852-43-3.mol

Synonyms:(3alpha,5alpha)-17-oxoandrostan-3-yl beta-D-glucopyranosiduronic acid;androsterone glucosiduronate;androsterone glucuronide;androsterone glucuronide, (3beta,5alpha)-isomer;androsterone glucuronide, (beta-D)-isomer;androsterone glucuronide, sodium salt, (3alpha,5alpha)-isomer;androsterone glucuronide, sodium salt, (3alpha,5beta)-isomer;etiocholanolone glucuronide

Suppliers and Price of Androsterone glucuronide

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

IsoSciences
AndrosteroneGlucuronideSodiumSalt ≥98%
10mg
$ 529.00

IsoSciences
AndrosteroneGlucuronideSodiumSalt ≥98%
5mg
$ 282.00

American Custom Chemicals Corporation
ANDROSTERONE GLUCURONIDE 95.00%
25MG
$ 1963.50

American Custom Chemicals Corporation
ANDROSTERONE GLUCURONIDE 95.00%
2.5MG
$ 715.00

Total 8 raw suppliers

Chemical Property of Androsterone glucuronide

Chemical Property:

Vapor Pressure:5.37E-20mmHg at 25°C
Boiling Point:656.1°Cat760mmHg
Flash Point:219.5°C
PSA：133.52000
Density:1.34g/cm³
LogP:1.87560
Storage Temp.:−20°C
XLogP3:2.3
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:3
Exact Mass:466.25666817
Heavy Atom Count:33
Complexity:801

Purity/Quality:

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

AndrosteroneGlucuronideSodiumSalt ≥98% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC12CCC(CC1CCC3C2CCC4(C3CCC4=O)C)OC5C(C(C(C(O5)C(=O)O)O)O)O
Isomeric SMILES:C[C@]12CC[C@H](C[C@@H]1CC[C@@H]3[C@@H]2CC[C@]4([C@H]3CCC4=O)C)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)C(=O)O)O)O)O

Technology Process of Androsterone glucuronide

There total 15 articles about Androsterone glucuronide 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: 73.0%

: (2S,3S,4S,5R,6R)-6-((3R,5S,8R,9S,10S,13S,14S)-10,13-Dimethyl-17-oxo-hexadecahydro-cyclopenta[a]phenanthren-3-yloxy)-3,4,5-tris-(2,2-dimethyl-propionyloxy)-tetrahydro-pyran-2-carboxylic acid methyl ester

: 1852-43-3
Androsterone glucuronide

Guidance literature:: With tetraethylammonium hydroxide; In isopropyl alcohol; at 20 ℃; for 168h;
DOI:10.1039/b412217h

Reference yield:

: 53-41-8
cis-androsterone

: 2616-64-0,7305-43-3,50722-58-2,106864-00-0,14520-48-0,30329-32-9,3545-73-1,5918-40-1
uridine diphosphoglucuronic acid

: 481-29-8
Epiandrosterone

: 846-46-8
androstanedione

: 1852-53-5
androstanediol

: 1852-43-3
5α-androstan-3α-ol-17-one-3-glucuronide

Guidance literature:: With phosphate buffer; PAPS; In ethanol; at 37 ℃; for 2h; Product distribution; 3H labeled, incubation of breast tissue homogenates from primary carcinoma, fibroadenoma, and metastasis to an axillary lymph node;
DOI:10.1016/0039-128X(81)90042-8