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Methidathion

From Wikipedia, the free encyclopedia
Methidathion
Names
Preferred IUPAC name
S-[(5-Methoxy-2-oxo-1,3,4-thiadiazol-3(2H)-yl)methyl]O,O-dimethyl phosphorodithioate
Other names
Supracide, Ultracide, Suprathion
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard100.012.227Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C6H11N2O4PS3/c1-10-5-7-8(6(9)16-5)4-15-13(14,11-2)12-3/h4H2,1-3H3 checkY
    Key: MEBQXILRKZHVCX-UHFFFAOYSA-N checkY
  • InChI=1/C6H11N2O4PS3/c1-10-5-7-8(6(9)16-5)4-15-13(14,11-2)12-3/h4H2,1-3H3
    Key: MEBQXILRKZHVCX-UHFFFAOYAL
  • O=C1SC(=N/N1CSP(=S)(OC)OC)\OC
Properties
C6H11N2O4PS3
Molar mass302.331 g/mol
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

Methidathion is anorganophosphateinsecticide;[1] its use is banned in the European Union and USA.[2]

Methidathion has been used as an insecticide in many countries to control caterpillars ofIndarbela quadrinotata.[3]

In 2012, residues were found in Thai vegetables at levels 100 times the legal limit.Thailand routinely uses many pesticides banned in the US and EU and in amounts far exceeding limits.[4]

References

[edit]
  1. ^Gokalp, Osman; Gulle, Kanat; Sulak, Osman; Cicek, Ekrem; Altuntas, Irfan (2016). "The effects of methidathion on liver: role of vitamins E and C".Toxicology and Industrial Health.19 (2–6):63–67.doi:10.1191/0748233703th176oa.PMID 15697176.S2CID 23209774.
  2. ^"Archived copy"(PDF). Archived fromthe original(PDF) on 2013-06-05. Retrieved2012-03-02.{{cite web}}: CS1 maint: archived copy as title (link)
  3. ^"CONTROL OF BARK EATING CATERPILLAR"(PDF). German Development Cooperation. Archived fromthe original(PDF) on 13 August 2016. Retrieved13 July 2016.
  4. ^"Nation Thailand news website, thai news, thailand news, Bangkok thailand, aec, breaking news : Nation Thailand". Archived fromthe original on August 25, 2012.

External links

[edit]
Carbamates
Inorganic compounds
Insect growth regulators
Neonicotinoids
Organochlorides
Organophosphorus
Pyrethroids
Diamides
Other chemicals
Metabolites
Biopesticides
Enzyme
(modulators)
ChATTooltip Choline acetyltransferase
AChETooltip Acetylcholinesterase
BChETooltip Butyrylcholinesterase
Transporter
(modulators)
CHTTooltip Choline transporter
VAChTTooltip Vesicular acetylcholine transporter
Release
(modulators)
Inhibitors
Enhancers


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