52864
Sodium 1-hexanesulfonate solution
suitable for ion pair chromatography, concentrate, LiChropur™, ampule
동의어(들):
1-Hexanesulfonic acid sodium salt
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
CH3(CH2)4CH2SO3Na
CAS 번호:
Molecular Weight:
188.22
UNSPSC Code:
23151816
NACRES:
NB.21
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3727014
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
SMILES string
[Na+].CCCCCCS([O-])(=O)=O
InChI key
QWSZRRAAFHGKCH-UHFFFAOYSA-M
description
anionic
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
Quality Level
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
저장 등급
10 - Combustible liquids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
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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