7a-Hydroxytestosterone

Base Information

Chemical Name:7a-Hydroxytestosterone
CAS No.:2141-17-5
Molecular Formula:C19H28O3
Molecular Weight:304.43
Hs Code.:
Mol file:2141-17-5.mol

Synonyms:7a-Hydroxytestosterone;D5-Androstene-3b,17a-diol;h_118_4_hydroxytestosterone;Androst-5-ene-3b,17a-diol;3b,17a-Dihydroxyandrost-5-ene;(3b,17a)-Androst-5-ene-3,17-diol;(17beta)-4,17-dihydroxy-Androst-4-en-3-one

Suppliers and Price of 7a-Hydroxytestosterone

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

American Custom Chemicals Corporation
4-HYDROXYTESTOSTERONE 95.00%
5MG
$ 495.81

Total 17 raw suppliers

Chemical Property of 7a-Hydroxytestosterone

Chemical Property:

Vapor Pressure:4.52E-11mmHg at 25°C
Melting Point:222-223 °C
Refractive Index:1.578
Boiling Point:476.3 °C at 760 mmHg
PKA:9.32±0.70(Predicted)
Flash Point:255.9 °C
PSA：57.53000
Density:1.19 g/cm³
LogP:3.76490
XLogP3:3.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:304.20384475
Heavy Atom Count:22
Complexity:551

Purity/Quality:

97% ^*data from raw suppliers

4-HYDROXYTESTOSTERONE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC12CCC3C(C1CCC2O)CCC4=C(C(=O)CCC34C)O
Isomeric SMILES:C[C@]12CCC3C(C1CC[C@@H]2O)CCC4=C(C(=O)CC[C@]34C)O
Uses 4-Hydroxytestosterone is an anabolic steroid and does not have any therapeutic indication. 4-Hydroxytestosterone is metabolite of the aromatase inhibitor Formestane (F692250). 4-Hydroxytestosterone co ncentration in the urine can be used as a biomarker for steroid misuse. Controlled Substance.

Technology Process of 7a-Hydroxytestosterone

There total 16 articles about 7a-Hydroxytestosterone 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: 78.0%

: 2189-83-5,6765-87-3,16318-53-9,17503-06-9,17503-07-0,17597-25-0,51154-10-0
(10R,13S,17S)-17-Hydroxy-10,13-dimethyl-tetradecahydro-20-oxa-cyclopropa[4,5]cyclopenta[a]phenanthren-3-one

: 2141-17-5,134523-13-0
4-Hydroxy-testosteron

Guidance literature:: With sulfuric acid; silica gel; acetic acid; at 70 ℃; for 0.05h;
DOI:10.1055/s-2007-985584

Reference yield: 50.0%

: 58-22-0
testosterone

: 2141-17-5
4-hydroxytestosterone

Guidance literature:: testosterone; With dihydrogen peroxide; sodium hydroxide; In methanol; at 4 ℃; for 24h;

With sulfuric acid; acetic acid; at 20 ℃; for 4h;