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H5269

Sigma-Aldrich

Sodium hexanesulfonate

≥98% (elemental analysis)

Synonym(s):

1-Hexanesulfonic acid sodium salt

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About This Item

Linear Formula:
C6H13O3SNa
CAS Number:
Molecular Weight:
188.22
EC Number:
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.21

description

anionic

Quality Level

assay

≥98% (elemental analysis)

mol wt

188.22 g/mol

technique(s)

protein purification: suitable

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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Application


  • Ion pair assisted micro matrix solid phase dispersion extraction of alkaloids from medical plant.: Sodium hexanesulfonate was used as an ion-pairing agent to improve the extraction efficiency of alkaloids from medicinal plants, providing a more effective extraction technique for phytochemical analysis (Dong et al., 2020).

  • Thermo-responsive draw solute for forward osmosis process; poly(ionic liquid) having lower critical solution temperature characteristics.: This research explored the use of Sodium hexanesulfonate in the development of a thermo-responsive draw solute for forward osmosis, contributing to advancements in water treatment technologies (Ju et al., 2019).

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Joana T Pinto et al.
International journal of pharmaceutics, 528(1-2), 416-428 (2017-06-18)
As pulmonary drug delivery is extended from low doses to high doses, physicochemical characteristics of the active pharmaceutical ingredient gain importance in the development of dry powder inhalers. Therefore, the present work aims to understand the impact of distinct engineering
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
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

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