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Stanozolol

Base Information Edit
  • Chemical Name:Stanozolol
  • CAS No.:302-96-5
  • Deprecated CAS:17966-55-1,69353-49-7,875293-72-4,302-96-5
  • Molecular Formula:C21H32N2O
  • Molecular Weight:328.498
  • Hs Code.:
  • European Community (EC) Number:233-894-8
  • NSC Number:43193
  • UNII:4R1VB9P8V3
  • DSSTox Substance ID:DTXSID3044128
  • Nikkaji Number:J332.003K,J3.432K
  • Wikipedia:Stanozolol
  • Wikidata:Q417219
  • NCI Thesaurus Code:C842
  • Pharos Ligand ID:TCP3J6JMNPCA
  • Metabolomics Workbench ID:38252
  • ChEMBL ID:CHEMBL2079587
  • Mol file:302-96-5.mol
Stanozolol

Synonyms:Androstanazol;Methylstanazol;Stanazolol;Stanozolol;Stromba;Winstrol

Suppliers and Price of Stanozolol
Supply Marketing:Edit
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
Total 11 raw suppliers
Chemical Property of Stanozolol Edit
Chemical Property:
  • Refractive Index:1.6500 (estimate) 
  • Boiling Point:490.8°Cat760mmHg 
  • Flash Point:250.7°C 
  • Density:1.129g/cm3 
  • XLogP3:4.5
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:0
  • Exact Mass:328.251463648
  • Heavy Atom Count:24
  • Complexity:538
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC12CCC3C(C1CCC2(C)O)CCC4C3(CC5=C(C4)NN=C5)C
  • Isomeric SMILES:C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@]2(C)O)CC[C@@H]4[C@@]3(CC5=C(C4)NN=C5)C
  • Recent ClinicalTrials:Hetrombopag for Low/Intermediate-1 Risk MDS With Thrombocytopenia
Technology Process of Stanozolol

There total 3 articles about Stanozolol 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:
17β-Hydroxy-3-oxo-17α-methyl-2-hydroxymethylen-androstan, N2H4*H2O, A., Sd., 2-6 Std.;
DOI:10.1021/ja01467a047
Guidance literature:
17β-Hydroxy-17α-methyl-androst-4-eno<3,2-c>pyrazol (VIb), Eisessig, Platin, Hydrierung;
Guidance literature:
5α-Androstanon-(17)-<3,2-c>-pyrazol, THF, aether. Methylmagnesiumbromid, Dampfbad;
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