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433063

Sigma-Aldrich

Sodium methanesulfinate

technical grade, 85%

Synonym(s):

Methanesulfinic acid sodium salt

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About This Item

Linear Formula:
CH3SO2Na
CAS Number:
Molecular Weight:
102.09
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

grade

technical grade

Quality Level

Assay

85%

mp

222-226 °C (dec.) (lit.)

functional group

sulfinic acid

SMILES string

[Na+].CS([O-])=O

InChI

1S/CH4O2S.Na/c1-4(2)3;/h1H3,(H,2,3);/q;+1/p-1

InChI key

LYPGDCWPTHTUDO-UHFFFAOYSA-M

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General description

Sodium methanesulfinate is an aliphatic sodium sulfinate. Conjugate addition of sodium methanesulfinate to vinyl heterocycles has been described. Cross-coupling reaction between aryl boronic acid and sodium methanesulfinate has been studied. Its stock solution was prepared from methanesulfonic acid by adding one equivalent of sodium hydroxide and diluting it to 4M.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Design, Synthesis and Discovery of 1-(2-(6-Chloro-3-methylsulfonyl)-naphthyl)-1H-pyrazole-5-carboxylamides as Highly Potent Factor Xa Inhibitors.
Jia ZJ, et al.
Chemical & Pharmaceutical Bulletin, 57(9), 1004-1007 (2009)
R Bruck et al.
Journal of hepatology, 35(4), 457-464 (2001-10-30)
Reactive oxygen species and oxidative stress were implicated in hepatic stellate cell activation and liver fibrosis. The aim of the present study was to examine whether the administration of free radical scavengers in vivo would prevent experimentally-induced hepatic cirrhosis in
A mild and efficient new synthesis of aryl sulfones from boronic acids and sulfinic acid salts.
Beaulieu C, et al.
Tetrahedron Letters, 45(16), 3233-3236 (2004)
Iodine-Catalyzed Oxidative Amination of Sodium Sulfinates: A Convenient Approach to the Synthesis of Sulfonamides under Mild Conditions.
Buathongjan C, et al.
European Journal of Organic Chemistry, 2015(7), 1575-1582 (2015)
Cecilia Arsene et al.
Environmental science & technology, 36(23), 5155-5163 (2003-01-14)
Dimethyl sulfoxide (CH3S(O)CH3: DMSO) is an important product of dimethyl sulfide (CH3SCH3: DMS) photooxidation. The mechanism of the OH-radical initiated oxidation of DMSO is still highly uncertain and a major aim of recent studies has been to establish if methane

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