Skip to Content
Merck
All Photos(3)

Documents

D5394

Sigma-Aldrich

Decyl β-D-glucopyranoside

≥98% (GC)

Synonym(s):

n-Decyl β-D-glucopyranoside

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C16H32O6
CAS Number:
Molecular Weight:
320.42
Beilstein:
85089
EC Number:
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.25

description

non-ionic

Assay

≥98% (GC)

form

powder

mol wt

320.42 g/mol

technique(s)

protein purification: suitable
protein quantification: suitable

color

white to off-white

CMC

2.2

solubility

methanol: 50 mg/mL, clear to very slightly hazy, colorless

storage temp.

−20°C

SMILES string

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

InChI

1S/C16H32O6/c1-2-3-4-5-6-7-8-9-10-21-16-15(20)14(19)13(18)12(11-17)22-16/h12-20H,2-11H2,1H3/t12-,13-,14+,15-,16-/m1/s1

InChI key

JDRSMPFHFNXQRB-IBEHDNSVSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Decyl β-D-glucopyranoside, a nonionic surfactant, is used in the development of sugar-based surfactant solutions. It may be used as a reference alkyl glucoside in separation and analysis procedures and to study its physiochemical properties and behavior as a surfactant.

Other Notes

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Atte J Kumpulainen et al.
Langmuir : the ACS journal of surfaces and colloids, 20(24), 10534-10541 (2004-11-17)
Surface tension isotherms were recorded for n-decyl-beta-d-glucopyranoside (Glu) and n-decyl-beta-D-maltopyranoside (Mal) solutions at temperatures of 8, 22, and 29 degrees C. Comparison was made with isotherms of n-decyl-beta-D-thiomaltopyranoside (S-Mal) at 22 degrees C. In addition to the transition from the
Annette Meister et al.
The journal of physical chemistry. B, 109(13), 6239-6246 (2006-07-21)
The adsorption of the surfactant n-nonyl-beta-D-glucopyranoside at the air-water interface after injection of the surfactant into the subphase was studied by infrared reflection absorption spectroscopy. In the first part, we investigated the equilibrium adsorption of n-nonyl-beta-D-glucopyranoside and the Gibbs adsorption
Atte J Kumpulainen et al.
Langmuir : the ACS journal of surfaces and colloids, 20(25), 10935-10942 (2004-12-01)
Measurements of surface tension isotherms were conducted for water solutions of pure and mixed n-decyl-beta-d-glucopyranoside (C(10)-Glu) and n-decyl-beta-d-maltopyranoside (C(10)-Mal) surfactants. By applying the Gibbs surface tension equation, the surface densities of Glu and Mal were derived for different compositions and
Henry Lam et al.
Biotechnology and bioengineering, 89(4), 381-392 (2005-01-12)
Liquid-liquid extraction in two-phase aqueous complex-fluid systems has been proposed as a scalable, versatile, and cost-effective purification method for the downstream processing of biotechnological products. In the case of two-phase aqueous micellar systems, careful choices of the phase-forming surfactants or
Francisco J Prado-Prado et al.
Bioorganic & medicinal chemistry, 18(6), 2225-2231 (2010-02-27)
There are many of pathogen parasite species with different susceptibility profile to antiparasitic drugs. Unfortunately, almost QSAR models predict the biological activity of drugs against only one parasite species. Consequently, predicting the probability with which a drug is active against

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service