Sodium methanesulfinate
Names
[ CAS No. ]:
20277-69-4
[ Name ]:
Sodium methanesulfinate
[Synonym ]:
sodium methyl sulfinate
Sodium methanesulfinate
Methanesulfinic acid, sodium salt (1:1)
Methanesulfinic Acid Sodium Salt
Sodiummethanesulphinate
MFCD00040392
sodium methanesulphinate
methanesulfinic acidsodium salt
Methanesulfinic Acid
Methanesulfinic acid,sodium salt
EINECS 243-669-6
Sodium methane sulfinate
Chemical & Physical Properties
[ Boiling Point ]:
256.4ºC at 760 mmHg
[ Melting Point ]:
222-226 °C (dec.)(lit.)
[ Molecular Formula ]:
CH3NaO2S
[ Molecular Weight ]:
102.088
[ Flash Point ]:
108.9ºC
[ Exact Mass ]:
101.975143
[ PSA ]:
59.34000
[ LogP ]:
0.36100
[ Water Solubility ]:
soluble
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H302
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xn:Harmful;
[ Risk Phrases ]:
R20/21/22
[ Safety Phrases ]:
S36/37
[ RIDADR ]:
2811
[ WGK Germany ]:
3
[ Packaging Group ]:
III
[ HS Code ]:
2930909090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2930909090
[ Summary ]:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
Articles
Biochemistry 53(22) , 3689-98, (2014)
Nitroxyl (HNO), a potential heart failure therapeutic, is known to target cysteine residues to form sulfinamides and/or disulfides. Because HNO-derived modifications may depend on their local environm...
Colorimetric assay for methanesulfinic acid in biological samples.Anal. Biochem. 163(1) , 67-73, (1987)
We describe a simple colorimetric method to measure 30 to 300 microM concentrations of sulfinic acids in biologic samples. The procedure employs the coupling reaction of an aromatic diazonium salt (Ar...
Modifiers of mercaptopyruvate sulfurtransferase catalyzed conversion of cyanide to thiocyanate in vitro.J. Biochem. Toxicol. 7(2) , 65-72, (1992)
The enzyme mercaptopyruvate sulfurtransferase appears to play an important role in the in vivo detoxification of cyanide. It does so by transferring sulfur to cyanide to produce thiocyanate, which is ...