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Merck
모든 사진(1)

문서

52864

Supelco

Sodium 1-hexanesulfonate solution

suitable for ion pair chromatography, concentrate, LiChropur, ampule

동의어(들):

1-Hexanesulfonic acid sodium salt

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About This Item

Linear Formula:
CH3(CH2)4CH2SO3Na
CAS Number:
Molecular Weight:
188.22
Beilstein:
3727014
MDL number:
UNSPSC 코드:
12000000
PubChem Substance ID:
NACRES:
NB.21

설명

anionic

Quality Level

품질

LiChropur
ampule

포장

ampule of 25 mL

기술

ion pair chromatography: suitable

λ

in concentrate

UV 흡수

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

적합성

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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일반 설명

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.

애플리케이션

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.

법적 정보

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

개인 보호 장비

Eyeshields, Gloves


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문서 라이브러리 방문

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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