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18842

Octyl-β-D-glucopyranoside 100 mM solution

Name: Octyl-β-<SC>D</SC>-glucopyranoside 100 mM solution
Brand: SIGMA

Synonym(s):

Octyl-β-D-glucopyranoside solution, Detergent Screening Solution 03/Kit-No 66317

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About This Item

CAS Number:

29836-26-8

NACRES:

NA.32

PubChem Substance ID:

329751747

UNSPSC Code:

12161902

MDL number:

MFCD00063288

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description

non-ionic

form

liquid

technique(s)

cell culture | insect: suitable, flow cytometry: suitable

storage temp.

2-8°C

SMILES string

CCCCCCCCO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

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

InChI key

HEGSGKPQLMEBJL-RKQHYHRCSA-N

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

Regulatory Information

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Biologically relevant lyotropic liquid crystalline phases in mixtures of n-octyl β-D-glucoside and water. Determination of the phase diagram by fluorescence spectroscopy.

Kerry K Karukstis et al.

The journal of physical chemistry. B, 116(12), 3816-3822 (2012-03-06)

When mixed with water, n-octyl β-D-glucoside forms self-assembled nanostructures, several of which are liquid crystalline and all of which depend on the water/glucoside ratio and temperature. For practical use of these phases, a detailed understanding of the conditions under which

Hydrogen bonds in galactopyranoside and glucopyranoside: a density functional theory study.

Zahrabatoul Mosapour Kotena et al.

Journal of molecular modeling, 19(2), 589-599 (2012-09-14)

Density functional theory calculations on two glycosides, namely, n-octyl-β-D-glucopyranoside (C(8)O-β-Glc) and n-octyl-β-D-galactopyranoside (C(8)O-β-Gal) were performed for geometry optimization at the B3LYP/6-31G level. Both molecules are stereoisomers (epimers) differing only in the orientation of the hydroxyl group at the C4 position.

Specific formation of trypsin-resistant micelles on a hydrophobic peptide observed with Triton X-100 but not with octylglucoside.

Chie Katsuda et al.

Biochimica et biophysica acta, 1798(11), 2090-2093 (2010-07-22)

The manner of interaction of the coat peptide of the Pf3 phage (Pf3 peptide) with lipid bilayers has been extensively studied. Presently, we designed a derivative of the Pf3 peptide, referred to as the DDRK peptide, and subjected it to

Complexity in molecular recognition.

Jörg Grunenberg

Physical chemistry chemical physics : PCCP, 13(21), 10136-10146 (2011-04-20)

The anomer selectivity of artificial carbohydrate receptors was studied using in silico methods in order to shed light on the thermodynamic driving forces at work during molecular recognition in general. The contributions of relevant intermolecular hydrogen bonds were investigated by

Resolving the challenge of measuring ligand binding to membrane proteins by combining analytical ultracentrifugation and light scattering photometry.

J D Doran et al.

Journal of pharmaceutical sciences, 101(1), 92-101 (2011-09-17)

Membrane proteins are attractive therapeutic targets, however the presence of detergents complicates biophysical binding measurements. Difficulties in determining quantitative dissociation constants for problematic membrane proteins were addressed by combining analytical ultracentrifugation and classical light scattering techniques. Validation of the algorithm

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Global Trade Item Number

SKU	GTIN
18842-1ML-F	04061838061881

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