N-octyl alpha-D-glucopyranoside

Modify Date: 2024-01-02 16:17:08

N-octyl alpha-D-glucopyranoside Structure
N-octyl alpha-D-glucopyranoside structure
Common Name N-octyl alpha-D-glucopyranoside
CAS Number 29781-80-4 Molecular Weight 292.36900
Density 1.18 g/cm3 Boiling Point 454.1ºC at 760 mmHg
Molecular Formula C14H28O6 Melting Point 110-112ºC
MSDS Chinese USA Flash Point 228.4ºC

 Use of N-octyl alpha-D-glucopyranoside


Octyl α-D-glucopyranoside is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name octyl α-D-glucopyranoside
Synonym More Synonyms

 N-octyl alpha-D-glucopyranoside Biological Activity

Description Octyl α-D-glucopyranoside is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog

 Chemical & Physical Properties

Density 1.18 g/cm3
Boiling Point 454.1ºC at 760 mmHg
Melting Point 110-112ºC
Molecular Formula C14H28O6
Molecular Weight 292.36900
Flash Point 228.4ºC
Exact Mass 292.18900
PSA 99.38000
LogP 0.16340
Vapour Pressure 3.72E-10mmHg at 25°C
Index of Refraction 1.515
Storage condition −20°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn
RIDADR NONH for all modes of transport
WGK Germany 3

 Synthetic Route

 Articles30

More Articles
Charged surfactants induce a non-fibrillar aggregation pathway of amyloid-beta peptide.

J. Pept. Sci. 19(9) , 581-7, (2013)

The amyloid β-peptide with a sequence of 42 amino acids is the major constituent of extracellular amyloid deposits in Alzheimer's disease plaques. The control of the peptide self-assembly is difficult...

Carbohydrate recognition and photodegradation by an anthracene-Kemp's acid hybrid.

Org. Biomol. Chem. 10(42) , 8393-5, (2012)

Selective recognition and photodegradation of a monosaccharide, octyl β-D-glucopyranoside, was achieved without any additives under neutral conditions using an anthracene-Kemp's acid hybrid and long-w...

Improved technique for reconstituting incredibly high and soluble amounts of tetrameric K⁺ channel in natural membranes.

J. Membr. Biol. 241(3) , 141-4, (2011)

The reconstitution of large amounts of integral proteins into lipid vesicles is largely prompted by the complexity of most biological membranes and protein stability. We optimized a particular system ...

 Synonyms

octyl alpha-D-glucopyranoside
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-octoxyoxane-3,4,5-triol
MFCD00070008