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Natrium-1-hexansulfonat -Lösung

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

Synonym(e):

1-Hexansulfonsäure Natriumsalz

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About This Item

Lineare Formel:
CH3(CH2)4CH2SO3Na
CAS-Nummer:
2832-45-3
Molekulargewicht:
188.22
Beilstein:
3727014
MDL-Nummer:
MFCD00007542
UNSPSC-Code:
12000000
PubChem Substanz-ID:
329757897
NACRES:
NB.21

Beschreibung

anionic

Qualitätsniveau

100

Qualität

LiChropur™
ampule

Verpackung

ampule of 25 mL

Methode(n)

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

Eignung

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

InChIKey

QWSZRRAAFHGKCH-UHFFFAOYSA-M

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Verwandte Kategorien

Allgemeine Beschreibung

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.

Anwendung

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.

Rechtliche Hinweise

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves

Choose from one of the most recent versions:

Analysenzertifikate (COA)

Lot/Batch Number
BCCK4799
BCCK0628
BCCF7533
BCCD8846
BCBS1928V

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Natrium-1-octansulfonat Monohydrat suitable for ion pair chromatography, LiChropur™, ≥99.0% (T)

Supelco

74882

Natrium-1-octansulfonat Monohydrat

1-Octansulfonsäure Natriumsalz ≥98%

Sigma-Aldrich

O8380

1-Octansulfonsäure Natriumsalz

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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