D5394
Decyl β-D-glucopyranoside
≥98% (GC)
别名:
n-Decyl β-D-glucopyranoside
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关于此项目
经验公式（希尔记法）:
C16H32O6
化学文摘社编号:
分子量:
320.42
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
EC Number:
261-469-7
Beilstein/REAXYS Number:
85089
MDL number:
产品名称
Decyl β-D-glucopyranoside, ≥98% (GC)
InChI key
JDRSMPFHFNXQRB-IBEHDNSVSA-N
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
SMILES string
CCCCCCCCCCO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
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
Quality Level
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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.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
涉药品监管产品
此项目有
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
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(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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