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この商品について
化学式:
CH3(CH2)9OSO3Na
CAS番号:
分子量:
260.33
UNSPSC Code:
41115711
NACRES:
NB.21
PubChem Substance ID:
EC Number:
205-568-5
Beilstein/REAXYS Number:
3576860
MDL number:
description
anionic
Quality Level
assay
≥99.0% (T)
form
flakes
quality
LiChropur™
technique(s)
ion pair chromatography: suitable
λ
10 % in H2O
UV absorption
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
suitability
corresponds to standard for filter test
SMILES string
[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
関連するカテゴリー
General description
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.
Application
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.
Legal Information
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2
保管分類
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
71443-VAR: + 71443-2.5G: + 71443-10G: + 71443-BULK:
jan
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
ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.
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