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6beta-Hydroxymethandrostenolone

Base Information
  • Chemical Name:6beta-Hydroxymethandrostenolone
  • CAS No.:33526-41-9
  • Molecular Formula:C26H44O3Si2
  • Molecular Weight:316.441
  • Hs Code.:
  • UNII:J37CM39S94
  • DSSTox Substance ID:DTXSID001043350
  • Metabolomics Workbench ID:38776
  • Nikkaji Number:J393.537J
  • Wikidata:Q27281125
  • Mol file:33526-41-9.mol
6beta-Hydroxymethandrostenolone

Synonyms:6beta-Hydroxymethandrostenolone;33526-41-9;6b-Hydroxymethandienone;6beta-Hydroxymethandienone;6beta-Hydroxydianabol;6beta-OH-Methandienone;J37CM39S94;6beta-Hydroxymetandienone;UNII-J37CM39S94;J393.537J;(6R,8R,9S,10R,13S,14S,17S)-6,17-dihydroxy-10,13,17-trimethyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-one;6beta-Hydroxymethandrostenolone, (-)-;(6beta,17beta)-6,17-Dihydroxy-17-methylandrosta-1,4-dien-3-one;(6S,17S)-10,13,17-trimethyl-6,17-bis(trimethylsilyloxy)-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-one;6.beta.-Hydroxymethandienone;6b-Hydroxydianabol;6b-Hydroxymethandrostenolone;6.BETA.-HYDROXYDIANABOL;6.BETA.-OH-METHANDIENONE;CHEBI:190894;DTXSID001043350;6.BETA.-HYDROXYMETANDIENONE;6.BETA.-HYDROXYMETHANDROSTENOLONE;PD076256;6.BETA.-HYDROXYMETHANDROSTENOLONE, (-)-;6b,17b-dihydroxy-17-methyl-Androsta-1,4-dien-3-one;Q27281125;(6b,17b)-6,17-dihydroxy-17-methyl-Androsta-1,4-dien-3-one;Androsta-1,4-dien-3-one, 6,17-dihydroxy-17-methyl-, (6beta,17beta)-;(6.BETA.,17.BETA.)-6,17-DIHYDROXY-17-METHYLANDROSTA-1,4-DIEN-3-ONE;ANDROSTA-1,4-DIEN-3-ONE, 6,17-DIHYDROXY-17-METHYL-, (6.BETA.,17.BETA.)-;(1S,2R,8R,10R,11S,14S,15S)-8,14-dihydroxy-2,14,15-trimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,6-dien-5-one

Suppliers and Price of 6beta-Hydroxymethandrostenolone
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
  • Cayman Chemical
  • 6β-hydroxy Metandienone ≥98%
  • 5mg
  • $ 483.00
  • Cayman Chemical
  • 6β-hydroxy Metandienone ≥98%
  • 1mg
  • $ 129.00
  • Cayman Chemical
  • 6β-hydroxy Metandienone ≥98%
  • 10mg
  • $ 772.00
  • American Custom Chemicals Corporation
  • 6-BETA-HYDROXYMETHANDIENONE 95.00%
  • 5MG
  • $ 502.56
  • AK Scientific
  • 6beta-Hydroxymethandrostenolone
  • 5mg
  • $ 702.00
Total 4 raw suppliers
Chemical Property of 6beta-Hydroxymethandrostenolone
Chemical Property:
  • Melting Point:28-29 °C(Solv: ethanol (64-17-5)) 
  • Boiling Point:481.9±45.0 °C(Predicted) 
  • PKA:13.79±0.70(Predicted) 
  • PSA:35.53000 
  • Density:1.19±0.1 g/cm3(Predicted) 
  • LogP:6.73450 
  • XLogP3:2.4
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:0
  • Exact Mass:316.20384475
  • Heavy Atom Count:23
  • Complexity:620
Purity/Quality:

99% *data from raw suppliers

6β-hydroxy Metandienone ≥98% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC12CCC3C(C1CCC2(C)O)CC(C4=CC(=O)C=CC34C)O
  • Isomeric SMILES:C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@]2(C)O)C[C@H](C4=CC(=O)C=C[C@]34C)O
  • Description 6β-hydroxy Metandienone(Item No. 24077) is an analytical reference standard categorized as an anabolic androgenic steroid metabolite of metandienone . This product is intended for research and forensic applications.
  • Uses 6β-Hydroxymethandrostenolone, is a metabolite of Methandrostenolone (M226000), an orally-effective anabolic steroid, being popular among bodybuilders.
Technology Process of 6beta-Hydroxymethandrostenolone

There total 6 articles about 6beta-Hydroxymethandrostenolone 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:
Guidance literature:
With Penicillium notatum KCH 904; In water; acetone; at 27 ℃; for 264h; Enzymatic reaction;
DOI:10.1016/j.steroids.2004.11.011
Guidance literature:
With human P450 3A4 monooxygenase; In methanol; aq. phosphate buffer; dimethyl sulfoxide; at 28 ℃; for 24h; pH=7.4; Enzymatic reaction;
DOI:10.1002/cctc.202101564
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