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CAS No 29836-26-8 , (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-octoxyoxane-3,4,5-triol

  • Name: (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-octoxyoxane-3,4,5-triol
  • Synonyms: B-Octylglucoside; Octyl-beta-D-glucopyranoside; 29836-26-8; OCTYL BETA-D-GLUCOPYRANOSIDE; Octyl beta-D-glucoside;(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-octoxyoxane-3,4,5-triol; n-Octyl glucoside;
  • CAS Registry Number:
  • Melting Point: 105 ºC
  • Density: 1.18 g/cm3
  • Refractive index: -27 ° (C=1, MeOH)
  • Alpha: -32 º (C=5, WATER)
  • Water Solubility: 3 G/10 ML
  • Safety Statements: S24/25
  • EINECS: 249-887-8
  • Molecular Weight: 292.36852
  • InchiKey: HEGSGKPQLMEBJL-RKQHYHRCSA-N
  • InChI: InChI=1S/C14H28O6/c1-2-3-4-5-6-7-8-19-14-13(18)12(17)11(16)10(9-15)20-
    14/h10-18H,2-9H2,1H3/t10-,11-,12+,13-,14-/m1/s1
  • Risk Statements: S24/25
  • Molecular Formula: C14H28O6
  • Molecular Structure:CAS No:29836-26-8 (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-octoxyoxane-3,4,5-triol

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29836-26-8 1-O-N-OCTYL-BETA-D-GLUCOPYRANOSIDE

  • Germany CHEMOS GmbH [Manufacturer]
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29836-26-8 A2834 OCTYL B-D-GLUCOPYRANOSIDE

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29836-26-8 1-O-OCTYL-SS-D-GLUCOPYRANOSIDE; 96%

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29836-26-8 1-O-N-Octyl-Beta-D-Glucopyranoside

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29836-26-8 OCTYL--D-GLUCOPYRANOSIDE

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29836-26-8 OCTYL-B-D-GLUCOPYRANOSIDE, N-(RG)

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29836-26-8 O-2000 N-OCTYL-BETA-D-GLUCOPYRANOSIDE

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29836-26-8 N-OCTYL--D-GLUCOSIDE

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29836-26-8 1-O-OCTYL-SS-D-GLUCOPYRANOSIDE

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29836-26-8 1-O-octyl-β-D-glucopyranoside

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References of (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-octoxyoxane-3,4,5-triol
Title: n-Octyl-b-D-glucoside
CAS Registry Number: 29836-26-8
CAS Name: Octyl-b-D-glucopyranoside
Synonyms: n-octylglucoside; OG
Molecular Formula: C14H28O6
Molecular Weight: 292.37
Percent Composition: C 57.51%, H 9.65%, O 32.83%
Literature References: Nonionic detergent primarily used for solubilizing membrane-bound proteins. Prepn: C. R. Noller, C. W. Rockwell, J. Am. Chem. Soc. 60, 2076 (1938). Partition behavior between water and membrane phases: M. Ueno, Biochemistry 28, 5631 (1989); thermodynamics and structural impact: M. R. Wenk et al., Biophys. J. 72, 1719 (1997). Solubilzation and reconstitution of liposomes: O. López et al., J. Phys. Chem. B 105, 9879 (2001). Solubilization of lipid vesicles: A. Meister, A. Blume, Phys. Chem. Chem. Phys. 6, 1551 (2004). Micelle formation: A. Walter et al., Biochim. Biophys. Acta 1508, 20 (2000); in mixed systems: A. Lainez et al., Langmuir 20, 5745 (2004).
Properties: White solid, mp 65-99°. [a]D25 -30.3° (methanol). Critical micelle concentration: 20-25 mM.
Melting point: mp 65-99°
Optical Rotation: [a]D25 -30.3° (methanol)
Use: Detergent and surfactant for biological systems.