H9026
Natriumhexansulfonat
BioXtra
Synonym(e):
Natrium-1-hexansulfonat Natriumsalz
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Alle Fotos(2)
About This Item
Lineare Formel:
C6H13O3SNa
CAS-Nummer:
Molekulargewicht:
188.22
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12161900
PubChem Substanz-ID:
NACRES:
NA.21
Empfohlene Produkte
Beschreibung
anionic
Qualitätsniveau
Produktlinie
BioXtra
Mol-Gew.
188.22 g/mol
Methode(n)
HPLC: suitable
Verunreinigungen
<0.001% Phosphorus (P)
<0.1% Insoluble matter
Löslichkeit
H2O: 0.1 M at 20 °C, clear, colorless
Kationenspuren
Al: <0.0005%
Ca: <0.0005%
Cu: <0.0005%
Fe: <0.0005%
K: <0.005%
Mg: <0.0005%
NH4+: <0.05%
Pb: <0.001%
Zn: <0.0005%
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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Anwendung
<ul>
<li><strong>Ion pair assisted micro matrix solid phase dispersion extraction of alkaloids from medical plant</strong>: Sodium hexanesulfonate was used as an ion-pairing reagent in the extraction of alkaloids for pharmacological studies, demonstrating its efficacy in enhancing the selectivity and sensitivity of HPLC methods in the analysis of complex plant matrices (Dong et al., 2020).</li>
<li><strong>Pharmacokinetic Properties of Arsenic Species after Intravenous and Intragastrical Administration of Arsenic Trioxide Solution in Cynomolgus Macaques Using HPLC-ICP-MS</strong>: This study highlights the role of Sodium hexanesulfonate in improving the chromatographic profiles of arsenic species, which is crucial for accurate pharmacokinetic assessment in pharmaceutical research (Shi et al., 2019).</li>
<li><strong>Organic solvent-free reversed-phase ion-pairing liquid chromatography coupled to atomic fluorescence spectrometry for organoarsenic species determination in several matrices</strong>: Sodium hexanesulfonate is utilized as a solvent-free ion-pairing agent, enabling greener analytical processes without compromising the performance of liquid chromatography systems (Monasterio et al., 2011).</li>
</ul>
<li><strong>Ion pair assisted micro matrix solid phase dispersion extraction of alkaloids from medical plant</strong>: Sodium hexanesulfonate was used as an ion-pairing reagent in the extraction of alkaloids for pharmacological studies, demonstrating its efficacy in enhancing the selectivity and sensitivity of HPLC methods in the analysis of complex plant matrices (Dong et al., 2020).</li>
<li><strong>Pharmacokinetic Properties of Arsenic Species after Intravenous and Intragastrical Administration of Arsenic Trioxide Solution in Cynomolgus Macaques Using HPLC-ICP-MS</strong>: This study highlights the role of Sodium hexanesulfonate in improving the chromatographic profiles of arsenic species, which is crucial for accurate pharmacokinetic assessment in pharmaceutical research (Shi et al., 2019).</li>
<li><strong>Organic solvent-free reversed-phase ion-pairing liquid chromatography coupled to atomic fluorescence spectrometry for organoarsenic species determination in several matrices</strong>: Sodium hexanesulfonate is utilized as a solvent-free ion-pairing agent, enabling greener analytical processes without compromising the performance of liquid chromatography systems (Monasterio et al., 2011).</li>
</ul>
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 2
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
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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
Miriam Gochin et al.
Journal of medicinal chemistry, 52(14), 4338-4344 (2009-06-19)
The hydrophobic pocket within the coiled coil domain of HIV-1 gp41 is considered to be a hot-spot suitable for small molecule intervention of fusion, although so far it has yielded only microM inhibitors. Previous peptide studies have identified specific hydrophobic
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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