Oxymesterone

Base Information

• Chemical Name: Oxymesterone
• CAS No.: 145-12-0
• Molecular Formula: C20H30O3
• Molecular Weight: 318.456
• Hs Code.: 2937290023
• European Community (EC) Number: 205-646-9
• NSC Number: 45048
• UNII: 4R73K9MRMX
• DSSTox Substance ID: DTXSID80878527
• Nikkaji Number: J5.832G
• Wikipedia: Oxymesterone
• Wikidata: Q10859626
• NCI Thesaurus Code: C74112
• Metabolomics Workbench ID: 38800
• ChEMBL ID: CHEMBL1908006
• Mol file: 145-12-0.mol

Synonyms:17alpah-methyl-4, 17beta-dihydroxy-androst-4-ene-3-one;oxymesterone

Chemical Property of Oxymesterone

Chemical Property:

• Vapor Pressure: 4.83E-11mmHg at 25°C
• Melting Point: 166-169°C
• Refractive Index: 1.573
• Boiling Point: 475.6°C at 760mmHg
• PKA: 9.32±0.70(Predicted)
• Flash Point: 255.5°C
• PSA: 57.53000
• Density: 1.17g/cm³
• LogP: 4.15500
• Storage Temp.: Controlled Substance, -20?C Freezer, Under Inert Atmosphere
• XLogP3: 3.2
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 318.21949481
• Heavy Atom Count: 23
• Complexity: 594

Purity/Quality:

99%, ^*data from raw suppliers

OXYMESTERONE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC12CCC(=O)C(=C1CCC3C2CCC4(C3CCC4(C)O)C)O
• Isomeric SMILES: C[C@]12CCC(=O)C(=C1CC[C@@H]3[C@@H]2CC[C@]4([C@H]3CC[C@]4(C)O)C)O
• Uses: An anabolic steroid.
• Therapeutic Function: Anabolic, Androgen

Technology Process of Oxymesterone

There total 7 articles about Oxymesterone 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:

4.17β-Dihydroxy-17α-methyl-androstadien-(4.6)-on-(3) (2320-90-3) → oxymesterone (145-12-0)

Guidance literature:

With hydrogen; palladium on activated charcoal; In ethanol;

Reference yield:

17-methyltestosterone (58-18-4) → oxymesterone (145-12-0)

Guidance literature:

Multi-step reaction with 2 steps

1: KOtBu / 2-methyl-propan-2-ol

2: H₂ / Pd-C / ethanol

With potassium tert-butylate; hydrogen; palladium on activated charcoal; In ethanol; tert-butyl alcohol;

Reference yield:

4-chloro-17α-methylandrost-4-en-17β-ol-3-one (5785-58-0) → oxymesterone (145-12-0)

Guidance literature:

Multi-step reaction with 2 steps

1: KOtBu / 2-methyl-propan-2-ol

2: H₂ / Pd-C / ethanol

With potassium tert-butylate; hydrogen; palladium on activated charcoal; In ethanol; tert-butyl alcohol;

upstream raw materials:

4.17β-Dihydroxy-17α-methyl-androstadien-(4.6)-on-(3)

17-methyltestosterone

4-chloro-17α-methylandrost-4-en-17β-ol-3-one