52865
1-Hexanesulfonate de sodium monohydrate
≥98.0% (T)
Synonyme(s) :
Acide 1-hexanesulfonique sodium salt monohydrate
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A propos de cet article
Formule linéaire :
CH3(CH2)4CH2SO3Na · H2O
Numéro CAS:
Poids moléculaire :
206.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
220-601-3
Beilstein/REAXYS Number:
3727014
MDL number:
Assay:
≥98.0% (T)
Form:
solid
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Laissez-nous vous aiderInChI key
CLCGFJYKZGFGSQ-UHFFFAOYSA-M
InChI
1S/C6H14O3S.Na.H2O/c1-2-3-4-5-6-10(7,8)9;;/h2-6H2,1H3,(H,7,8,9);;1H2/q;+1;/p-1
SMILES string
O.[Na+].CCCCCCS([O-])(=O)=O
assay
≥98.0% (T)
form
solid
functional group
sulfonic acid
Quality Level
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Catégories apparentées
General description
Sodium 1-pentanesulfonate monohydrate, also known as 1-Hexanesulfonic acid sodium salt monohydrate, is commonly used as a surfactant and a reversed-phase ion-pairing agent.
Application
Sodium 1-hexanesulfonate monohydrate can be used as a catalyst to synthesize:
It can also be used as a reactant to prepare polynuclear oxidobismuth sulfonates by reacting with sodium 2-methyl-2-propensulfonate and tetra-μ3-hydroxyhexakis(nitrato-κO)tetra-μ3-oxohexabismuth in DMSO.
- Amidoalkyl naphthols by three-component reaction of β-naphthol, aldehydes, and urea.
- Aminophosphonates by the reaction of aldehydes/ketones with amines.
It can also be used as a reactant to prepare polynuclear oxidobismuth sulfonates by reacting with sodium 2-methyl-2-propensulfonate and tetra-μ3-hydroxyhexakis(nitrato-κO)tetra-μ3-oxohexabismuth in DMSO.
Classe de stockage
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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.
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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
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
Ana L Costa et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(34), 12069-12078 (2015-07-29)
Zn-Al layered double hydroxides (LDHs) containing solely indigo carmine (IC) or 1-hexanesulfonate (HS) anions, or a mixture of the two with different HS/IC molar ratios, were prepared by the direct synthesis method and characterized by various techniques. Hydrotalcite-type phases were
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