89720
Sodium p-toluenesulfinate
purum, anhydrous, ≥96.0% (NT)
Synonym(s):
p-Toluenesulfinic acid sodium salt
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About This Item
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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
11 - Combustible Solids
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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
Acta biomaterialia, 6(1), 63-71 (2009-07-01)
Conductive neural interfaces tailored for cell interaction by incorporation of bioactive factors are hypothesized to produce superior neuroprostheses with improved charge transfer capabilities. This study examined the effect of entrapping nerve growth factor (NGF) within the conducting polymer poly(ethylene dioxythiophene)
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
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
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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