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Merck
CN

V900365

Octyl β-D-glucopyranoside

Vetec™, reagent grade, 98%

Synonym(s):

n-Octyl glucoside, OGP

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About This Item

Empirical Formula (Hill Notation):
C14H28O6
CAS Number:
29836-26-8
Molecular Weight:
292.37
EC Number:
249-887-8
UNSPSC Code:
12161900
PubChem Substance ID:
329829777
Beilstein/REAXYS Number:
84118
MDL number:
MFCD00063288

Key Documents

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InChI key

HEGSGKPQLMEBJL-RKQHYHRCSA-N

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

SMILES string

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

grade

reagent grade

description

non-ionic

product line

Vetec™

assay

98%

mol wt

micellar avg mol wt 25,000

aggregation number

84

CMC

20-25 mM (20-25°C)

transition temp

cloud point >100 °C

storage temp.

−20°C

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Application

Non-ionic, dialyzable detergent for the solubilization and isolation of membrane proteins. Has been shown to increase the resolution of proteins in 2D gels.

Legal Information

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

涉药品监管产品
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Certificates of Analysis (COA)

Lot/Batch Number
WXBF7963V
WXBF7045V
WXBF5290V
WXBF4994V
WXBF1706V

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Christine Ménager et al.
Langmuir : the ACS journal of surfaces and colloids, 26(19), 15453-15463 (2010-09-10)
The present study deals with the morphological modifications of giant dioleoyl phosphatidylcholine vesicles (DOPC GUVs) induced by the nonionic surfactant n-octyl β,D-glucopyranoside at sublytic levels, i.e., in the first steps of the vesicle-to-micelle transition process, when surfactant inserts into the
Chaoqun Yao et al.
Proteomics. Clinical applications, 4(1), 4-16 (2010-12-08)
About two million new cases of leishmaniasis with 50 000 associated deaths occur worldwide each year. Promastigotes of the causative Leishmania spp. develop from the procyclic stage to the highly virulent metacyclic stage within the sand fly vector. We hypothesized
M Sakai et al.
Colloids and surfaces. B, Biointerfaces, 80(2), 107-115 (2010-07-17)
A new technique of the jet drop method (JDM) was applied to a chiral molecular discrimination of optically active D- or L-glucose (guest) by chiral N-octyl-beta-D-glycoside (ObetaDG)-Cu(II) complex (host) at the gas/liquid interface of small bubbles. The discrimination of glucoses
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
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.
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