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
Beilstein:
3574491
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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 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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Véronique Fournier et al.
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Journal of chromatography. A, 1214(1-2), 30-36 (2008-11-14)
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A variety of pyrazolo[3,4-d]pyrimidine-6(7H)-thione derivatives were easily synthesized with a novel, simple, efficient, and regioselective method via three-component condensation reaction of 5-methyl-1H-pyrazol-3-amine, arylisothiocyanates, and aldehydes in the presence of catalytic amount of p-toluenesulfonic acid (p-TSA) in 1-butyl-3-methylimidazolium bromide ionic liquid
Synthesis of p-toluenesulfinic esters of cellulose and beta-cyclodextrin.
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Dental materials journal, 28(4), 401-408 (2009-09-02)
In this study, a dual-curing type composite resin cement that included a photo-initiator and two accelerators was designed. In particular, special emphasis was made on addressing questions on the effects from different amounts of additional accelerators on the flexural strength
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