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52864

Supelco

Sodium 1-hexanesulfonate solution

suitable for ion pair chromatography, concentrate, LiChropur™, ampule

Sinonimo/i:

1-Hexanesulfonic acid sodium salt

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About This Item

Formula condensata:
CH3(CH2)4CH2SO3Na
Numero CAS:
2832-45-3
Peso molecolare:
188.22
Beilstein:
3727014
Numero MDL:
MFCD00007542
Codice UNSPSC:
12000000
ID PubChem:
329757897
NACRES:
NB.21

Descrizione

anionic

Livello qualitativo

100

Qualità

LiChropur™
ampule

Confezionamento

ampule of 25 mL

tecniche

ion pair chromatography: suitable

λ

in concentrate

Assorbanza UV

λ: 210 nm Amax: 0.07
λ: 220 nm Amax: 0.04
λ: 230 nm Amax: 0.03
λ: 260 nm Amax: 0.01
λ: 500 nm Amax: 0.01

Compatibilità

corresponds to standard for RP gradient test
corresponds to standard for filter test

Stringa SMILE

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

InChI

1S/C6H14O3S.Na/c1-2-3-4-5-6-10(7,8)9;/h2-6H2,1H3,(H,7,8,9);/q;+1/p-1
QWSZRRAAFHGKCH-UHFFFAOYSA-M

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Descrizione generale

Concentrate for 6x1 L ready-to-use solution. Dilute contents of one ampule (~0.3 M) to 1 L with HPLC grade water to obtain a 0.005 M eluent solution.

Applicazioni

Sodium 1-hexanesulfonate may be used as an ion-pairing reagent for the determination of L-carnitine in food supplement formulations by ion-pair chromatography with indirect conductimetric detection.

Note legali

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves

Choose from one of the most recent versions:

Certificati d'analisi (COA)

Lot/Batch Number
BCCL3643
BCCK4799
BCCK0628
BCCF7533
BCCD8846

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1-ottano solfonato di sodio suitable for ion pair chromatography, LiChropur™, ≥99.0% (T)

Supelco

74882

1-ottano solfonato di sodio

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Sigma-Aldrich

O8380

Acido 1-ottano solfonico

Determination of L-carnitine in food supplement formulations using ion-pair chromatography with indirect conductimetric detection
Kakou A, et al.
Journal of Chromatography A, 1069(2), 209-215 (2005)
Philip Zakaria et al.
Electrophoresis, 23(17), 2821-2832 (2002-09-11)
The separation of a series of aromatic carboxylic acids, sulfonates and opiates using electrokinetic chromatography employing a mixture of the soluble cationic polymer poly(diallydimethylammonium chloride) (PDDAC) and the amphiphilic anion hexanesulfonate as pseudostationary phases is described. In this system, the
Kirti S Niralwad et al.
Ultrasonics sonochemistry, 17(5), 760-763 (2010-03-17)
1-Hexanesulphonic acid sodium salt was found to be an efficient catalyst for the green synthesis of alpha-aminophosphonates by the coupling of aldehydes/ketone, an amine and triethyl phosphite under ultrasound irradiation at ambient temperature for appropriate time to furnish the desired
A R Calhoun et al.
Journal of colloid and interface science, 309(2), 505-510 (2007-03-03)
Measurements have been made to determine the solubility of ethane, C2H6, in aqueous solutions of four different surfactants of the linear alkanesulfonate class at 25 degrees C. The surfactants, sodium 1-pentanesulfonate, sodium 1-hexanesulfonate, sodium 1-heptanesulfonate, and sodium 1-octanesulfonate, all share
R Salazar-González et al.
Molecular biology reports, 41(12), 7833-7843 (2014-08-29)
Arylamine N-acetyltransferase 2 (NAT2) metabolizes isoniazid (INH) and Single Nucleotide Polymorphisms (SNP) responsible for its activity has been reported. The aim of this study in the Mexican mestizo population was to evaluate NAT2 expression at the protein level in immune
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