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D5394

Sigma-Aldrich

Decyl β-D-glucopyranoside

≥98% (GC)

Sinónimos:

n-Decyl β-D-glucopyranoside

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About This Item

Fórmula empírica (notación de Hill):
C16H32O6
Número de CAS:
58846-77-8
Peso molecular:
320.42
Beilstein/REAXYS Number:
85089
EC Number:
261-469-7
MDL number:
MFCD00063297
UNSPSC Code:
12352201
PubChem Substance ID:
24893830
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

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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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

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Sigma-Aldrich

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n-Dodecil β-D-maltósido

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
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
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
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

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