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52864

Supelco

Sodium 1-hexanesulfonate solution

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

Synonym(s):

1-Hexanesulfonic acid sodium salt

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About This Item

Linear Formula:
CH3(CH2)4CH2SO3Na
CAS Number:
2832-45-3
Molecular Weight:
188.22
Beilstein:
3727014
MDL number:
MFCD00007542
UNSPSC Code:
12000000
PubChem Substance ID:
329757897
NACRES:
NB.21

description

anionic

Quality Level

100

quality

LiChropur™
ampule

packaging

ampule of 25 mL

technique(s)

ion pair chromatography: suitable

λ

in concentrate

UV absorption

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

suitability

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

SMILES string

[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

InChI key

QWSZRRAAFHGKCH-UHFFFAOYSA-M

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General description

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.

Application

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.

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL3643
BCCK4799
BCCK0628
BCCF7533
BCCD8846

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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)
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
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
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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