Potassium thioacetate
Names
[ CAS No. ]:
10387-40-3
[ Name ]:
Potassium thioacetate
[Synonym ]:
Thioacetic acid, potassium salt
Potassium thioacetate
Potassium Thioacetic
Thioacetic acid potassium salt
potassium thiacetate
S-POTASSIUM THIOACETATE
MeCOSK
MFCD00083065
thiolacetic acid potassium salt
Potasium thioacetate
Potassium thioacete
KTAA
Potassium thioacetat
Potassiumthioacetate
Ethanethioic acid, potassium salt (1:1)
EINECS 233-848-7
Potassium ethanethioate
Ethanethioic acid, potassium salt
Thioacetic Acid S-Potassium Salt
Potassium thioethanoate
POTASSIUM THIOLACETATE
K-thioacetate
ethanethioic acid potassium salt
Chemical & Physical Properties
[ Density]:
1.046g/cm3
[ Boiling Point ]:
130.6ºC at 760 mmHg
[ Melting Point ]:
173-176 °C(lit.)
[ Molecular Formula ]:
C2H3KOS
[ Molecular Weight ]:
114.208
[ Flash Point ]:
32.8ºC
[ Exact Mass ]:
113.954170
[ PSA ]:
17.07000
[ LogP ]:
0.07980
[ Storage condition ]:
Refrigerator (+4°C)
[ Water Solubility ]:
soluble
MSDS
Safety Information
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xi:Irritant
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S26-S36-S37/39
[ RIDADR ]:
UN 3335
[ WGK Germany ]:
3
[ Packaging Group ]:
II; III
[ Hazard Class ]:
4.1
[ 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
J. Fluoresc. 25 , 777-85, (2015)
A coumarin-terminated self-assembled monolayer on silver particles (C-SAM) from the reduction of silver ions in the presence of compound 3 was successfully prepared by utilizing phase transfer method,...
A novel approach for high sensitive determination of sulfur mustard by derivatization and isotope-dilution LC-MS/MS analysis.Talanta 132 , 245-51, (2014)
A new isotope-dilution liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for determination of sulfur mustard (SM) has been developed using a direct chemical derivatization method by nuc...
Transformation of thiodiglycol by resting cells of Alcaligenes xylosoxydans PGH10.Biotechnol. Prog. 18(2) , 252-6, (2002)
A new strain of Alcaligenes xylosoxydans able to aerobically cometabolize thiodiglycol, the primary hydrolysis product of sulfur mustard, was isolated and tested in a laboratory scale stirred tank rea...