Score: #2 in Biophysics , #1774 in Physics , #2120 in Biochemistry , #5515 in Chemistry

  Consumer Ingredient · Pharmaceutical

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Suppliers

• Sigma-Aldrich - 29836-26-8
  25.20 - 979.00 USD
• Fisher Scientific - Search for 29836-26-8
• TCI - 29836-26-8
  62.00 - 210.00 USD

Most-cited Publications

• Binding of an octylglucoside detergent molecule in the second substrate (S2) site of LeuT establishes an inhibitor-bound conformation (Proceedings of the National Academy of Sciences of the United States of America, 2009)
• Micellar properties of octylglucoside in aqueous solutions (Journal of Colloid and Interface Science, 1990)
• The effects of octylglucoside on the Semliki forest virus membrane. Evidence for a spike-protein--nucleocapsid interaction. (FEBS Journal, 1980)
• Action of octylglucoside on non-ionic monoalkyl amphiphile-cholesterol vesicles : study of the solubilization mechanism (Chemistry and Physics of Lipids, 1990)
• Solubilization and reconstitution of vesicular stomatitis virus envelope using octylglucoside (Biophysical Journal, 1997)
• Demonstration of phosphatidylinositol anchors on Ly-6 molecules by specific phospholipase C digestion and gel electrophoresis in octylglucoside (Biochemical and Biophysical Research Communications, 1987)

Areas of Application

Safety

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Trends

Alternate Names

• octylglucoside
• octyl glucoside
• octyl-D-glucoside, (alpha)-isomer
• beta-octyl-D-glucoside
• octyl-beta-D-glucoside
• octyl-alpha-D-glucoside
• 1-O-n-octyl-beta-D-glucopyranoside
• beta-octylglucopyranoside
• N-octyl-beta-D-glucopyranoside
• octylglucopyranoside
• SMILES
  CCCCCCCCOC1C(C(C(C(O1)CO)O)O)O
• InChIKey
  HEGSGKPQLMEBJL-UHFFFAOYSA-N

External Links

• Pubchem - 29836-26-8
• Wikipedia - caprylyl glucoside
  Octyl glucoside (n-octyl--D-glucoside) is a nonionic surfactant frequently used to solubilise integral membrane proteins for studies in biochemistry. Structurally, it is a glycoside derived from glucose and octanol. Like Genapol X-100 and Triton X-100, it is a nonphysiological amphiphile that makes lipid bilayers less "stiff".

Synthesis

Similar Compounds

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