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N7507

Sigma-Aldrich

Nonyl β-D-glucopyranoside

≥97.0% (GC)

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Empirical Formula (Hill Notation):
C15H30O6
CAS Number:
69984-73-2
Molecular Weight:
306.40
Beilstein:
12168
MDL number:
MFCD00063300
UNSPSC Code:
12352201
PubChem Substance ID:
24897830
NACRES:
NA.25

description

non-ionic

Quality Level

200

Assay

≥97.0% (GC)

form

powder

mol wt

306.40 g/mol

CMC

6.5

storage temp.

−20°C

SMILES string

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

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

InChI key

QFAPUKLCALRPLH-UXXRCYHCSA-N

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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.

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

监管及禁止进口产品

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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

Solubilization of Membrane Proteins

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