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Merck
CN

N7507

Nonyl β-D-glucopyranoside

≥97.0% (GC)

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About This Item

Empirical Formula (Hill Notation):
C15H30O6
CAS Number:
Molecular Weight:
306.40
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
12168
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InChI

1S/C15H30O6/c1-2-3-4-5-6-7-8-9-20-15-14(19)13(18)12(17)11(10-16)21-15/h11-19H,2-10H2,1H3/t11-,12-,13+,14-,15-/m1/s1

SMILES string

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

InChI key

QFAPUKLCALRPLH-UXXRCYHCSA-N

description

non-ionic

assay

≥97.0% (GC)

form

powder

mol wt

306.40 g/mol

CMC

6.5

storage temp.

−20°C

Quality Level

General description

Nonyl β-D-glucopyranoside is a nonionic surfactant among a small number of surfactants found to be useful for the solubilization and crystallization of a large number of biological membrane proteins.

Application

Nonyl β-D-glucopyranoside has been used in a study to assess the structure and molecular fluctuations of n-alkyl-β-d-glucopyranoside micelles. It has also been used in a study to investigate enantiomer separation of drugs by micellar electrokinetic chromatography.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

涉药品监管产品
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Structure and Molecular Fluctuations of n-Alkyl-β-d-glucopyranoside Micelles Determined by X-ray and Neutron Scattering
Zhang, R., et al.
Langmuir, 15, 7510-7519 (1999)
K Otsuka et al.
Journal of chromatography. A, 875(1-2), 163-178 (2000-06-06)
A review surveying enantiomer separations by micellar electrokinetic chromatography (MEKC) using chiral surfactants is described. MEKC is one of the most popular techniques in capillary electrophoresis, where neutral compounds can be analyzed as well as charged ones, and the use
Parmjeet Randhawa et al.
Antimicrobial agents and chemotherapy, 51(12), 4492-4494 (2007-09-26)
BK virus is an important pathogen in kidney transplant recipients. In vitro studies demonstrated slight antiviral activity for chloroquine and nystatin. A sialic acid derivative, BTB11968, was identified as a lead compound for further development.

Protocols

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