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Merck
CN

71443

Supelco

癸烷基硫酸钠

suitable for ion pair chromatography, LiChropur, ≥99.0% (T)

别名:

硫酸癸酯 钠盐

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About This Item

线性分子式:
CH3(CH2)9OSO3Na
CAS号:
分子量:
260.33
Beilstein:
3576860
EC 号:
MDL编号:
UNSPSC代码:
12000000
PubChem化学物质编号:
NACRES:
NB.21

描述

anionic

质量水平

检测方案

≥99.0% (T)

形式

flakes

质量

LiChropur

技术

ion pair chromatography: suitable

λ

10 % in H2O

紫外吸收

λ: 210 nm Amax: 0.05
λ: 220 nm Amax: 0.04
λ: 230 nm Amax: 0.03
λ: 260 nm Amax: 0.02
λ: 500 nm Amax: 0.02

适用性

corresponds to standard for filter test

SMILES字符串

[Na+].CCCCCCCCCCOS([O-])(=O)=O

InChI

1S/C10H22O4S.Na/c1-2-3-4-5-6-7-8-9-10-14-15(11,12)13;/h2-10H2,1H3,(H,11,12,13);/q;+1/p-1

InChI key

XZTJQQLJJCXOLP-UHFFFAOYSA-M

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一般描述

Sodium decyl sulfate is an anionic surfactant. It is a sodium salt monodecyl ester of sulfuric acid. It also has application in textile, leather and other industries as emulsifier, wetting agent, dispersant, fiber lubricant, and synthetic fatliquor.

应用

Sodium decyl sulfate was used in a study conducted to investigate the preferential interaction of poly(vinylpyrrolidone) (PVP) toward the alkyl sulfate surfactants using 13C and 1H NMR and NOESY measurements.

法律信息

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

象形图

CorrosionExclamation mark

警示用语:

Danger

危险声明

危险分类

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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G. W. A. Milne
Gardner's Commercially Important Chemicals: Synonyms, Trade Names, and Properties, 560-560 (2005)
Binding of sodium decyl sulfate to a cationic polymer.
Shirahama, Keishiro, Hidefumi Yuasa, and Shinji Sugimoto.
Bulletin of the Chemical Society of Japan, 54.2, 375-377 (1981)
Complex formation between poly (vinylpyrrolidone) and sodium decyl sulfate studied through NMR.
Roscigno, Paola, et al.
Langmuir, 19.23, 9638-9644 (2003)
Miriam Gochin et al.
Journal of medicinal chemistry, 52(14), 4338-4344 (2009-06-19)
The hydrophobic pocket within the coiled coil domain of HIV-1 gp41 is considered to be a hot-spot suitable for small molecule intervention of fusion, although so far it has yielded only microM inhibitors. Previous peptide studies have identified specific hydrophobic
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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