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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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The Journal of organic chemistry, 74(10), 4009-4012 (2009-04-24)
2-Arylchromans were readily prepared from the hetero-Diels-Alder reactions of styrenes with the ortho-quinone methides (o-QMs) which, in turn, were generated by treating the MOM-protected benzylacetate derivatives with p-TsOH immobilized on silica (PTS-Si) in toluene under mild conditions (0 degrees C
W Dong et al.
Hua xi yi ke da xue xue bao = Journal of West China University of Medical Sciences = Huaxi yike daxue xuebao, 21(3), 277-280 (1990-09-01)
Using biotinylated human Y-specific DNA probe PHY2.1 and Cos 84, we carried out Southern and dot hybridization with human DNA from artificially aborted chorionic villi, and with DNA of peripheral lymphocytes from normal male and female. The results show that
Véronique Fournier et al.
Journal of chromatography. A, 1129(1), 21-28 (2006-08-09)
Addition of long-chain polyunsaturated fatty acids (LC-PUFAs) from marine oil into food products implies preliminary refining procedures of the oil which thermal process affects the integrity of LC-PUFAs. Deodorization, the major step involving high temperatures, is a common process used
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

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