Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

Tibolone

Base Information Edit
  • Chemical Name:Tibolone
  • CAS No.:5630-53-5
  • Deprecated CAS:133677-19-7
  • Molecular Formula:C21H28O2
  • Molecular Weight:312.452
  • Hs Code.:
  • European Community (EC) Number:227-069-1
  • UNII:FF9X0205V2
  • DSSTox Substance ID:DTXSID5023667
  • Nikkaji Number:J8.033K
  • Wikipedia:Tibolone
  • Wikidata:Q413805
  • NCI Thesaurus Code:C66955
  • Pharos Ligand ID:XJ1V3BSSG221
  • Metabolomics Workbench ID:54520
  • ChEMBL ID:CHEMBL2103774
  • Mol file:5630-53-5.mol
Tibolone

Synonyms:Boltin;Livial;Liviella;Org OD 14;Org OD14;tibilone;tibolone

Suppliers and Price of Tibolone
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
  • Sigma-Aldrich
  • Tibolone ≥98% (HPLC)
  • 50 mg
  • $ 49.90
  • Sigma-Aldrich
  • Tibolone for system suitability European Pharmacopoeia (EP) Reference Standard
  • y0000668
  • $ 190.00
  • Cayman Chemical
  • Tibolone
  • 5000mg
  • $ 324.00
  • Cayman Chemical
  • Tibolone ≥98%
  • 100mg
  • $ 17.00
  • Cayman Chemical
  • Tibolone ≥98%
  • 500mg
  • $ 65.00
  • Cayman Chemical
  • Tibolone
  • 1000mg
  • $ 98.00
  • AvaChem
  • Tibolone
  • 100mg
  • $ 75.00
  • AvaChem
  • Tibolone
  • 10mg
  • $ 35.00
  • AvaChem
  • Tibolone
  • 1g
  • $ 175.00
  • American Custom Chemicals Corporation
  • TIBOLONE 95.00%
  • 100MG
  • $ 1871.10
Total 134 raw suppliers
Chemical Property of Tibolone Edit
Chemical Property:
  • Appearance/Colour:white solid 
  • Vapor Pressure:6.96E-10mmHg at 25°C 
  • Melting Point:169 °C 
  • Refractive Index:105 ° (C=0.54, CH2Cl2/Et2O) 
  • Boiling Point:447.4 °C at 760 mmHg 
  • PKA:13.10±0.60(Predicted) 
  • Flash Point:190.6 °C 
  • PSA:37.30000 
  • Density:1.13 g/cm3 
  • LogP:3.88260 
  • Storage Temp.:2-8°C 
  • Solubility.:DMSO: soluble15mg/mL, clear 
  • XLogP3:2.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:312.208930132
  • Heavy Atom Count:23
  • Complexity:636
Purity/Quality:

99%, *data from raw suppliers

Tibolone ≥98% (HPLC) *data from reagent suppliers

Safty Information:
  • Pictogram(s): Dangerous
  • Hazard Codes:
  • Statements: 51/53 
  • Safety Statements: 22-24/25-61 
MSDS Files:

SDS file from LookChem

Useful:
  • Drug Classes:Synthetic Estrogen
  • Canonical SMILES:CC1CC2=C(CCC(=O)C2)C3C1C4CCC(C4(CC3)C)(C#C)O
  • Isomeric SMILES:C[C@@H]1CC2=C(CCC(=O)C2)[C@@H]3[C@@H]1[C@@H]4CC[C@]([C@]4(CC3)C)(C#C)O
  • Recent ClinicalTrials:The Effects of Luo-Bu-Fu-Ke-Bi-RI Pill on Climacteric Syndrome in Women
  • Recent EU Clinical Trials:A Multicenter, Randomized, Double-Blind, Placebo- And Active-Controlled Study of DVS-233 SR for Treatment of Vasomotor Symptoms Associated with Menopause
  • Description Tibolone is a synthetic steroid with weak progestational and estrogenic properties, reportedly useful in controlling symptoms resulting from natural or surgical menopause. It has thus far shown no significant antithrombotic effect in post-menopausal patients.
  • Uses A synthetic steroid with weak estrogenic, androgenic and progestogenic activity. A pharamceutical used in the treatment of menopausal syndrome
  • Clinical Use Tibolone is a synthetic steroid that has been shown to increase bone mineral density similar to alendronate. The U.S. FDA approval is pending; overseas, this agent is used for the treatment of menopausal symptoms as well as the prevention of osteoporosis. It is considered to be a viable alternative to conjugated equine estrogen plus micronized progesterone.
Technology Process of Tibolone

There total 24 articles about Tibolone 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: 90.0%

Guidance literature:
With sulfuric acid; In water; acetone; at 0 - 5 ℃; for 1h; Industrial scale;
Guidance literature:
3-Methoxy-7α-methyl-17α-aethinyl-17β-hydroxy-Δ2,5(10)-19-norandrastadien; With ascorbic acid; In ethanol; at 20 - 30 ℃; for 1h; Activated Carbon Darco G60;
With hydrogenchloride; In ethanol; water; at 20 - 25 ℃;
Refernces Edit
Post RFQ for Price