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Squalene-2,3-diol

Base Information
  • Chemical Name:Squalene-2,3-diol
  • CAS No.:14031-37-9
  • Molecular Formula:C30H52 O2
  • Molecular Weight:444.742
  • Hs Code.:
  • Mol file:14031-37-9.mol
Squalene-2,3-diol

Synonyms:(?à)-Squalene-2,3-diol;2,3-Dihydroxysqualene; Squalene glycol; Squalene-2,3-glycol

Suppliers and Price of Squalene-2,3-diol
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
  • TRC
  • Squalene-2,3-glycol
  • 10mg
  • $ 165.00
  • Medical Isotopes, Inc.
  • Squalene-2,3-glycol
  • 50 mg
  • $ 900.00
  • Arctom
  • Squalene-2,3-diol ≥98%
  • 5mg
  • $ 463.00
Total 19 raw suppliers
Chemical Property of Squalene-2,3-diol
Chemical Property:
  • Boiling Point:550.9±38.0 °C(Predicted) 
  • PKA:14.66±0.29(Predicted) 
  • PSA:40.46000 
  • Density:0.914±0.06 g/cm3(Predicted) 
  • LogP:8.77060 
  • Storage Temp.:Refrigerator 
  • Solubility.:Chloroform, Dichloromethane, Ethyl Acetate 
Purity/Quality:

99.5% *data from raw suppliers

Squalene-2,3-glycol *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses Squalene-2,3-glycol is an intermediate in the enzymic conversion of squalene to lanosterol and cholesterol, and a precursor in the chemical synthesis of different squalene oxides.
Technology Process of Squalene-2,3-diol

There total 6 articles about Squalene-2,3-diol 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:
Multi-step reaction with 3 steps
1: NBS; H2O / tetrahydrofuran
2: K2CO3 / methanol
3: 3 percent aq. HClO4 / 1,2-dimethoxy-ethane
With N-Bromosuccinimide; perchloric acid; water; potassium carbonate; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; 1: hydroxybromination / 2: Epoxidation / 3: Hydrolysis;
DOI:10.1021/ja993054l
Guidance literature:
Multi-step reaction with 2 steps
1: K2CO3 / methanol
2: 3 percent aq. HClO4 / 1,2-dimethoxy-ethane
With perchloric acid; potassium carbonate; In methanol; 1,2-dimethoxyethane; 1: Epoxidation / 2: Hydrolysis;
DOI:10.1021/ja993054l
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