Methenolone

Base Information

Chemical Name:Methenolone
CAS No.:153-00-4
Molecular Formula:C20H30O2
Molecular Weight:302.457
Hs Code.:2937290019
European Community (EC) Number:205-812-0
UNII:9062ZT8Q5C
DSSTox Substance ID:DTXSID10165179
Nikkaji Number:J11.393J
Wikipedia:Metenolone
Wikidata:Q905078
NCI Thesaurus Code:C175130
Metabolomics Workbench ID:35330
Mol file:153-00-4.mol

Synonyms:Metenolone;Methenolone

Suppliers and Price of Methenolone

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

Biosynth Carbosynth
Methenolone
50 mg
$ 350.00

Biosynth Carbosynth
Methenolone
10 mg
$ 125.00

AHH
Methenolone 98%
0.05g
$ 446.00

Total 69 raw suppliers

Chemical Property of Methenolone

Chemical Property:

Vapor Pressure:3.26E-09mmHg at 25°C
Melting Point:126-129°C(lit.)
Refractive Index:1.542
Boiling Point:430.381 °C at 760 mmHg
PKA:15.08±0.70(Predicted)
Flash Point:183.597 °C
PSA：37.30000
Density:1.084 g/cm³
LogP:4.12520
XLogP3:3.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:302.224580195
Heavy Atom Count:22
Complexity:536

Purity/Quality:

99%, ^*data from raw suppliers

Methenolone ^*data from reagent suppliers

Safty Information:

Pictogram(s): C
Hazard Codes:C

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=O)CC2C1(C3CCC4(C(C3CC2)CCC4O)C)C
Isomeric SMILES:CC1=CC(=O)C[C@H]2[C@]1([C@H]3CC[C@]4([C@H]([C@@H]3CC2)CC[C@@H]4O)C)C
Uses Methenolone is an anabolic steroid. This is a controlled substance.
Therapeutic Function 17β-Hydroxy-1β-methyl-5α-androst-l-ene-3-one acetate

Technology Process of Methenolone

There total 7 articles about Methenolone 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:

: methenolone enanthate

: 153-00-4
17β-hydroxy-1-methyl-5α-androst-1-en-3-one

Guidance literature:: With Cunninghamella blakesleeana; In methanol; at 26 ℃; for 288h; Microbiological reaction;
DOI:10.1016/j.steroids.2016.04.007