Nonyl b-D-glucopyranoside

Nonyl b-D-glucopyranoside

Catalog Number:
D001144835BIO
Mfr. No.:
DN03173
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      • Overview
        • Nonyl β-D-glucopyranoside is an alkylglycoside non-ionic mild detergent used for cell lysis and membrane protein isolation. As it is uncharged it is unlikely to cause protein denaturation or refolding issues, allowing for the isolation of intact macromolecular complexes without affecting protein-protein interactions. Nonyl β-D-glucopyranoside is useful for the solubilization and crystallization of many biological membrane proteins and isolation of membrane-bound proteins. It has also been used for enantiomeric separation by capillary electrophoresis. Nonyl β-D-glucopyranoside is also known as B-Nonylglucoside or Nonyl D-glucoside and has an aggregation number of 133. It is dialyzable from membrane protein preparations and has a Critical Micelle Concentration (CMC) of 6.5mM.

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      • Properties
        • CAS Number
          69984-73-2
          Molecular Formula
          C15H30O6
          Molecular Weight
          306.4 g/mol
          MDL Number
          MFCD00063300
          Note
          There is no hazardous surcharge associated with this product.
          There is no special packaging charge associated with this product.

          * For research use only. Not for human or veterinary use

      • Reference
        • deGrip et al (1979). Synthesis and properties of alkylglucosides with mild detergent action: improved synthesis and purification of β-1-octyl-, -nonyl-, and -decyl-glucose. Synthesis of β-1-undecylglucose and β-1-dodecylmaltose. Chemistry and Physics of Lipids 23(4):321-335.
          Chung et al (1989). The lyotropic liquid crystal properties of n-octyl 1-O-beta-D-glucopyranoside and related n-alkyl pyranosides. Biochimica et biophysica acta 985(3):300–306.
          Mechref et al (1997) Capillary electrophoresis of herbicides II. Evaluation of alkylglucoside chiral surfactants in the enantiomeric separation of phenoxy acid herbicides. Journal of Chromatography A 757(1–2):263-273.
          Otsuka et al (2000) Enantiomer separation of drugs by micellar electrokinetic chromatography using chiral surfactants. Journal of Chromatography A 875(1–2) 163-178.

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