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89720

Sigma-Aldrich

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
Beilstein:
3574491
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

grade

purum

Assay

≥96.0% (NT)

form

powder

SMILES string

[Na+].Cc1ccc(cc1)S([O-])=O

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

InChI key

KFZUDNZQQCWGKF-UHFFFAOYSA-M

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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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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
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)
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
C Bernofsky et al.
Free radical research communications, 9(3-6), 303-315 (1990-01-01)
Adenosine and its nucleotides react with hypochlorite to form unstable products that have been identified as the N6 chloramine derivatives. These chloramines spontaneously oligomerize, form stable adducts with proteins and nucleic acids, and are converted with loss of chlorine to
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

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