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D3412

Sigma-Aldrich

Sodium 1-decanesulfonate

~98%

Synonyme(s) :

Acide 1-décanesulfonique sodium salt

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About This Item

Formule linéaire :
CH3(CH2)8CH2SO3Na
Numéro CAS:
13419-61-9
Poids moléculaire :
244.33
Numéro Beilstein :
3918920
Numéro CE :
236-525-9
Numéro MDL:
MFCD00007526
Code UNSPSC :
12161900
ID de substance PubChem :
24893753
Nomenclature NACRES :
NA.25

Description

anionic

Pureté

~98%

Forme

powder

Poids mol.

244.33 g/mol

Technique(s)

LC/MS: suitable

Pf

>300 °C (lit.)

Chaîne SMILES 

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

InChI

1S/C10H22O3S.Na/c1-2-3-4-5-6-7-8-9-10-14(11,12)13;/h2-10H2,1H3,(H,11,12,13);/q;+1/p-1

Clé InChI

AIMUHNZKNFEZSN-UHFFFAOYSA-M

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Description générale

Sodium 1-decanesulfonate is an anionic surfactant that is used for the analysis of organic small molecule compounds by HPLC and by ion-pair liquid chromatography. The anionic sulfonate counterion permits the separation and resolution of positively charged analytes. The critical micelle concentration (CMC) of sodium 1-decanesulfonate is assessed using capillary electrophoresis. Some studies report the interactions between hydroxypropylmethylcellulose and several ionic surfactants, like sodium 1-decanesulfonate.

Application

Sodium 1-decanesulfonate has been used in a study to assess the mechanism of Zn2+ ions electroreduction. It has also been used in a study to investigate the retention mechanism of guanidine compounds on a porous graphitic carbon.
Réactifs d′association d′ions en HPLC, y compris pour l′analyse des peptides et des protéines

Caractéristiques et avantages

  • Suitable for high-performance liquid chromatography (HPLC) and ion-pair liquid chromatography
  • Allows the separation and resolution of positively charged analytes.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

Certificats d'analyse (COA)

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Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 769(2), 261-268 (2002-05-09)
A micellar electrokinetic capillary chromatography (MEKC) for determining fluoxetine and its metabolite (norfluoxetine) is proposed. Optimal conditions for the quantitative separation were investigated. A background electrolyte solution consisting of 5 mM phosphate buffer adjusted to pH 12.3 and 40 mM
Y Inamoto et al.
Journal of chromatography. B, Biomedical sciences and applications, 707(1-2), 111-120 (1998-06-05)
The retention mechanism of guanidino compounds on a porous graphitic carbon seemed to be mainly hydrophobic interaction, according to the retention factors in buffer solutions and the results of an analysis by computational chemical calculation using molecular mechanics (MM2). The
W A Moats
Journal of agricultural and food chemistry, 48(6), 2244-2248 (2000-07-11)
A simplified procedure was developed for determination of tetracycline antibiotics in tissues which improved stability of these compounds in sample extracts and eliminated the need for troublesome cleanup procedures. Tissues were homogenized in water. Acetonitrile (16 mL) and then 1
Influence of sodium 1-decanesulfonate on the enthalpy of activation of two-step Zn2+ ions electroreduction
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Journal of Electroanalytical Chemistry (Lausanne Switzerland), 662, 8-8 (2011)
N M Kovalchuk et al.
Journal of colloid and interface science, 459, 250-256 (2015-08-25)
Mixed solutions of cationic and anionic surfactants show considerable synergism in their wetting behaviour, but their spreading is affected considerably by the phase separation processes. The valuable information about wetting properties of synergetic mixtures can be obtained by using mixtures
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