60-51-5 MSDS - Dimethoate
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Dimethoate

Identification
Name Dimethoate
CAS Registry Number 60-51-5
Synonyms EL 12880;DIMETATE(R);DIMETHOATE;CHAMP;CEKUTOATE;DANADIM(R);CYGON;CYGON(R)
Molecular Structure Dimethoate   60-51-5
Molecular Formula C5H12NO3PS2
Molecular Weight 229.26
mp: 52-52.5℃
Hazard Codes: Details
Risk Statements: 21/22-63-43-36/37/38-23/24/25-45-36-20/21/22-11
Safety Statements: 2-36/37-24/25-23-53-26
RIDADR: UN 2783
Supplier
Lightchem Inc
Supply Precious metal catalyst
OLED Materials etc.
www.lightchem.com
 
Wiki & MSDS
60-51-5.pdf
Dimethoate
Dimethoate Structural Formulae .V.1.svg
Names
IUPAC name
O,O-dimethyl S-[2-(methylamino)-2-oxoethyl] dithiophosphate
Other names
O,O-dimethyl S-methylcarbamoylmethyl phosphorodithioate
Phosphorodithioic acid, O,O-Dimethyl S-(2-(methylamino)-2-oxoethylyl)ester
Identifiers
CAS Number
  • 60-51-5 YesY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:34714 YesY
ChemSpider
  • 2973 YesY
ECHA InfoCard 100.000.437
KEGG
  • C14326 YesY
PubChem CID
  • 3082
UNII
  • W6U08B045O YesY
Properties
Chemical formula
C5H12NO3PS2
Molar mass 229.26 g/mol
Appearance Grey-white crystalline solid
Density 1.3 g/cm3, solid
Melting point 43 to 45 °C (109 to 113 °F; 316 to 318 K)
Boiling point 117 °C (243 °F; 390 K) at 10 Pa
Solubility in water
2.5 g/100 ml
Hazards
Main hazards Highly toxic
Safety data sheet External MSDS
GHS pictograms GHS-pictogram-exclam.svg[1]
GHS hazard statements
H302 - H312[1]
GHS precautionary statements
P280[1]
Flash point 107 °C (225 °F; 380 K)
Related compounds
Related organophosphates
malathion
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Dimethoate is a widely used organophosphate insecticide and acaricide. It was patented and introduced in the 1950s by American Cyanamid. Like other organophosphates, dimethoate is an acetylcholinesterase inhibitor which disables cholinesterase, an enzyme essential for central nervous system function. It acts both by contact and through ingestion. It is readily absorbed and distributed throughout plant tissues, and is degraded relatively rapidly.[2]


 







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