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Octyl D-glucopyranoside

Base Information Edit
  • Chemical Name:Octyl D-glucopyranoside
  • CAS No.:41444-50-2
  • Deprecated CAS:6801-93-0
  • Molecular Formula:C14H28O6
  • Molecular Weight:292.373
  • Hs Code.:
  • European Community (EC) Number:259-216-0,255-367-1
  • DSSTox Substance ID:DTXSID1042235
  • Nikkaji Number:J470.599H
  • Wikipedia:Octyl_glucoside
  • Mol file:41444-50-2.mol
Octyl D-glucopyranoside

Synonyms:1-O-n-octyl-beta-D-glucopyranoside;beta-octyl-D-glucoside;beta-octylglucopyranoside;N-octyl-beta-D-glucopyranoside;octyl glucoside;octyl-alpha-D-glucoside;octyl-beta-D-glucoside;octyl-D-glucoside, (alpha)-isomer;octylglucopyranoside;octylglucoside

Suppliers and Price of Octyl D-glucopyranoside
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
  • American Custom Chemicals Corporation
  • OCTYL GLUCOSIDE 95.00%
  • 5MG
  • $ 497.39
Total 4 raw suppliers
Chemical Property of Octyl D-glucopyranoside Edit
Chemical Property:
  • Vapor Pressure:3.72E-10mmHg at 25°C 
  • Boiling Point:454.1±45.0 °C(Predicted) 
  • PKA:12.95±0.70(Predicted) 
  • Density:1.18±0.1 g/cm3(Predicted) 
  • XLogP3:1.4
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:9
  • Exact Mass:292.18858861
  • Heavy Atom Count:20
  • Complexity:250
Purity/Quality:

98%Min *data from raw suppliers

OCTYL GLUCOSIDE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Chemical Classes:Biological Agents -> Monosaccharides and Derivatives
  • Canonical SMILES:CCCCCCCCOC1C(C(C(C(O1)CO)O)O)O
  • Isomeric SMILES:CCCCCCCCOC1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O
Technology Process of Octyl D-glucopyranoside

There total 13 articles about Octyl D-glucopyranoside 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 phenylacetic acid; choline chloride; at 80 - 95 ℃; Reagent/catalyst; Catalytic behavior; Inert atmosphere; Green chemistry;
Guidance literature:
α-cellulose; With water; 1-butyl-3-methylimidazolium chloride; at 99.84 ℃; for 0.666667h; Acidic conditions;
octanol; at 89.84 ℃; for 24h; under 760.051 Torr;
DOI:10.1039/c0cc00031k
Guidance literature:
α-cellulose; With water; 1-butyl-3-methylimidazolium chloride; at 99.84 ℃; for 2.5h;
octanol; at 89.84 ℃; for 24h; under 30.003 Torr;
DOI:10.1039/c0cc00031k
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