89720
Sodium p-toluenesulfinate
purum, anhydrous, ≥96.0% (NT)
Synonym(s):
p-Toluenesulfinic acid sodium salt
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About This Item
Linear Formula:
4-CH3-C6H4SO2Na
CAS Number:
Molecular Weight:
178.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-538-5
Beilstein/REAXYS Number:
3574491
MDL number:
Product Name
Sodium p-toluenesulfinate, purum, anhydrous, ≥96.0% (NT)
InChI key
KFZUDNZQQCWGKF-UHFFFAOYSA-M
InChI
1S/C7H8O2S.Na/c1-6-2-4-7(5-3-6)10(8)9;/h2-5H,1H3,(H,8,9);/q;+1/p-1
SMILES string
[Na+].Cc1ccc(cc1)S([O-])=O
grade
purum
assay
≥96.0% (NT)
form
powder
functional group
sulfinic acid
Quality Level
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Related Categories
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Xianghong Li et al.
The journal of adhesive dentistry, 14(2), 129-136 (2011-09-22)
The use of sodium hypochlorite (NaOCl) can decrease the bond strength of 4-META/MMA-TBB resin cement to root dentin. The aim of this in vitro study was to evaluate the effect of sodium toluene sulfinic acid (SA) as a pretreatment to
T Lyubimova et al.
Electrophoresis, 14(1-2), 40-50 (1993-01-01)
Photopolymerization of polyacrylamide gels in the presence of methylene blue (100 microM) and a redox couple (1 mM sodium toluenesulfinate, a reducer, and 50 microM diphenyliodonium chloride, an oxidizer) has been investigated. The gel point, i.e. the time needed for
Xiaoxiang Zhang et al.
The Journal of organic chemistry, 75(18), 6290-6293 (2010-08-28)
A general and efficient method to prepare 2,4-di- and trisubstituted thiazoles via p-TsOH·H(2)O-catalyzed cyclization of trisubstituted propargylic alcohols with thioamides is described. The reaction was accomplished in moderate to excellent product yields under mild conditions that did not require the
K Eulitz et al.
Lipids, 34(8), 873-877 (1999-10-21)
Conjugated linoleic acid (CLA) mixtures were isomerized with p-toluenesulfinic acid or I2 catalyst. The resultant mixtures of the eight cis/trans geometric isomers of 8,10-, 9,11-, 10,12-, and 11,13-octadecadienoic (18:2) acid methyl esters were separated by silver ion-high-performance liquid chromatography (Ag+-HPLC)
Jumat Salimon et al.
Journal of biomedicine & biotechnology, 2011, 196565-196565 (2011-12-02)
For environmental reasons, a new class of environmentally acceptable and renewable biolubricant based on vegetable oils is available. In this study, oxirane ring opening reaction of monoepoxide linoleic acid (MEOA) was done by nucleophilic addition of oleic acid (OA) with
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