Skip to Content
Merck

D5394

Decyl β-D-glucopyranoside

≥98% (GC)

Synonym(s):

n-Decyl β-D-glucopyranoside

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):
C16H32O6
CAS Number:
Molecular Weight:
320.42
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
EC Number:
261-469-7
Beilstein/REAXYS Number:
85089
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


description

non-ionic

Quality Level

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

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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

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

Visit the Document Library



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
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
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