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Merck

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:
Assay:
≥96.0% (NT)
Form:
powder
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Quality Level

grade

purum

assay

≥96.0% (NT)

form

powder

functional group

sulfinic acid

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

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



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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
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
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



Global Trade Item Number

SKUGTIN
89720-500G04061833076545
89720-100G04061832420813