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triazophos

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triazophos

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Also known as O,O-diethyl O-(1-phenyl-1H-1,2,4-triazol-3-yl) thiophosphate, Triazofos, 1-Phenyl-1,2,4-triazolyl-3-(O,O-diethylthionophosphate), Phosphorothioic acid, O,O-diethyl O-(1-phenyl-1H-1,2,4-triazol-3-yl) ester, Hostathion, Methoxone

Triazofos is a chemical compound used in acaricides, insecticides, and nematicides.

Chemical data

Formula
C12H16N3O3PS
Molecular weight
313.31 g/mol
IUPAC name
diethoxy-[(1-phenyl-1,2,4-triazol-3-yl)oxy]-sulfanylidene-lambda5-phosphane
SMILES
CCOP(=S)(OCC)OC1=NN(C=N1)C2=CC=CC=C2
InChIKey
AMFGTOFWMRQMEM-UHFFFAOYSA-N
XLogP
3.5
Polar surface area
90.5 Ų
H-bond donors
0
H-bond acceptors
6
Formal charge
0

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Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Mass
313.065
Show 2 more facts
chemical formula
C₁₂H₁₆N₃O₃PS
canonical SMILES
CCOP(=S)(OCC)OC1=NN(C=N1)C2=CC=CC=C2
Sources (2)

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~11 min read

Encyclopedic overview

16 sections
Contents
  • History
  • Synthesis and available forms
  • Synthesis
  • Available forms
  • Chemical properties
  • Structure and reactivity
  • Metabolism and mechanisms of action
  • Metabolism
  • Effects on animals
  • Mechanism of action
  • Efficacy and toxicity
  • Efficacy
  • Toxicity
  • Adverse effects and health hazards in humans
  • Antidote
  • References

Triazofos is a chemical compound used in acaricides, insecticides, and nematicides.

== History == Triazofos has been registered in the Federal Office of Consumer Protection and Food Safety since 1975 and authorized as an insecticide in the EU until 31 December 2004 (Commission Regulation No 2076/2002). As of 25 July 2003 it was revoked under Commission Regulation No 1336/2003. The production of triazofos began in the 1980s as a Hoechst patent by the company Bayer. In 2011 Bayer announced termination of the sale of this product, due to its poisonous properties.

Excerpted from Wikipedia’s “triazophos” article, available under the CC BY-SA 4.0 licence.

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