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8-Hexadecanol

Base Information Edit
  • Chemical Name:8-Hexadecanol
  • CAS No.:19781-83-0
  • Molecular Formula:C16H34O
  • Molecular Weight:242.445
  • Hs Code.:2905199090
  • Mol file:19781-83-0.mol
8-Hexadecanol

Synonyms:octyl-octanol;Heptyloctylcarbinol;n-Hexadecanol-8;8-Hexadecanol;

Suppliers and Price of 8-Hexadecanol
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 7 raw suppliers
Chemical Property of 8-Hexadecanol Edit
Chemical Property:
  • Vapor Pressure:8.34E-05mmHg at 25°C 
  • Refractive Index:1.4278 (estimate) 
  • Boiling Point:304.4oC at 760 mmHg 
  • Flash Point:117.8oC 
  • PSA:20.23000 
  • Density:0.834g/cm3 
  • LogP:5.45840 
  • Water Solubility.:Soluble in water. 
Purity/Quality:

98%Min *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Statements: 36/37/38 
  • Safety Statements: 26-36/37/39 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 8-Hexadecanol

There total 18 articles about 8-Hexadecanol 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 sodium tetrahydroborate; In tetrahydrofuran; methanol; at 0 - 20 ℃; for 1.5h;
Guidance literature:
n-hexylmagnesium chloride; 3-n-octyl-2,5-dioxathiolane 1,1-dioxide; With dilithium tetrachlorocuprate; In tetrahydrofuran; at 20 ℃; for 1h;
With sulfuric acid; In tetrahydrofuran; water; for 12h; chemoselective reaction;
DOI:10.1021/acs.orglett.6b01745
Guidance literature:
With glucose dehydrogenase from Bacillus megaterium; cytochrome P450 monooxygenase CYP505E3 from Aspergillus terreus; nicotinamide adenine dinucleotide; In aq. phosphate buffer; at 25 ℃; for 24h; regioselective reaction; Enzymatic reaction;
DOI:10.1002/anie.202001055
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