52865
Sodium 1-hexanesulfonate monohydrate
≥98.0% (T)
동의어(들):
1-Hexanesulfonic acid sodium salt monohydrate
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모든 사진(2)
About This Item
Linear Formula:
CH3(CH2)4CH2SO3Na · H2O
CAS Number:
Molecular Weight:
206.24
Beilstein:
3727014
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
분석
≥98.0% (T)
양식
solid
작용기
sulfonic acid
SMILES string
O.[Na+].CCCCCCS([O-])(=O)=O
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
InChI key
CLCGFJYKZGFGSQ-UHFFFAOYSA-M
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일반 설명
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.
애플리케이션
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.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
이미 열람한 고객
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
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
Mixtures of catanionic surfactants can be superspreaders: Comparison with trisiloxane superspreader.
N M Kovalchuk et al.
Journal of colloid and interface science, 459, 250-256 (2015-08-25)
Mixed solutions of cationic and anionic surfactants show considerable synergism in their wetting behaviour, but their spreading is affected considerably by the phase separation processes. The valuable information about wetting properties of synergetic mixtures can be obtained by using mixtures
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