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H9026

Sigma-Aldrich

Sodium hexanesulfonate

BioXtra

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Synonym(s):
1-Hexanesulfonic acid sodium salt
Linear Formula:
C6H13O3SNa
CAS Number:
Molecular Weight:
188.22
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.21

description

anionic

Quality Level

product line

BioXtra

mol wt

188.22 g/mol

technique(s)

HPLC: suitable

impurities

<0.001% Phosphorus (P)
<0.1% Insoluble matter

solubility

H2O: 0.1 M at 20 °C, clear, colorless

cation traces

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

InChI key

QWSZRRAAFHGKCH-UHFFFAOYSA-M

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This Item
H52695286452862
Sodium hexanesulfonate BioXtra

Sigma-Aldrich

H9026

Sodium hexanesulfonate

Premium Grade
Sodium hexanesulfonate &#8805;98% (elemental analysis)

Sigma-Aldrich

H5269

Sodium hexanesulfonate

-
product line

BioXtra

product line

-

product line

-

product line

-

mol wt

188.22 g/mol

mol wt

188.22 g/mol

mol wt

-

mol wt

206.24 g/mol

technique(s)

HPLC: suitable

technique(s)

protein purification: suitable

technique(s)

ion pair chromatography: suitable

technique(s)

ion pair chromatography: suitable

impurities

<0.001% Phosphorus (P), <0.1% Insoluble matter

impurities

-

impurities

-

impurities

-

solubility

H2O: 0.1 M at 20 °C, clear, colorless

solubility

-

solubility

-

solubility

-

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
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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
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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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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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