Misplaced Pages

Chlorfenvinphos

Article snapshot taken from[REDACTED] with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.

This is an old revision of this page, as edited by 84.56.152.174 (talk) at 10:50, 23 June 2011. The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Revision as of 10:50, 23 June 2011 by 84.56.152.174 (talk)(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)
Chlorfenvinphos
Names
IUPAC name Phosphoric acid diethyl ester
Other names Birlane, Dermaton, Sapercon, Steladone, Supona
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.006.758 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C12H14Cl3O4P/c1-3-17-20(16,18-4-2)19-12(8-13)10-6-5-9(14)7-11(10)15/h5-8H,3-4H2,1-2H3/b12-8-Key: FSAVDKDHPDSCTO-WQLSENKSSA-N
  • InChI=1/C12H14Cl3O4P/c1-3-17-20(16,18-4-2)19-12(8-13)10-6-5-9(14)7-11(10)15/h5-8H,3-4H2,1-2H3/b12-8-Key: FSAVDKDHPDSCTO-WQLSENKSBC
SMILES
  • Clc1cc(Cl)ccc1C(OP(=O)(OCC)OCC)=Cl
Properties
Chemical formula C12H14Cl3O4P
Molar mass 359.57 g/mol
Appearance Amber liquid
Solubility in water 145 mg/L
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Chemical compound

Chlorfenvinphos is an organophosphorus compound that was widely used as an insecticide but has been banned in several countries. It is a colorless solid, but for commercial purposes, it was marketed as an amber liquid. Its use in the U.S. was cancelled in 1991. Chlorfenvinphos was sold under several brand names.

The molecule can be described as an enol ester derived from dichloroacetophenone and diethylphosphonic acid. The molecule hydroyzes in the environment.

Safety

The substance has harmful effects on the nervous system. The LD50 is 15  mg/kg (rats, oral).

References

  1. Robert L. Metcalf “Insect Control” in Ullmann’s Encyclopedia of Industrial Chemistry” Wiley-VCH, Weinheim, 2002. doi:10.1002/14356007.a14_263
  2. Chlorfenvinphos summary from U.S. Agency for Toxic Substances and Disease Registry

External links

Pest control: Insecticides
Carbamates
Inorganic compounds
Insect growth regulators
Neonicotinoids
Organochlorides
Organophosphorus
Pyrethroids
Diamides
Other chemicals
Metabolites
Biopesticides
Acetylcholine receptor modulators
Muscarinic acetylcholine receptor modulators
mAChRsTooltip Muscarinic acetylcholine receptors
Agonists
Antagonists
Precursors
(and prodrugs)
See also
Receptor/signaling modulators
Nicotinic acetylcholine receptor modulators
Acetylcholine metabolism/transport modulators
Nicotinic acetylcholine receptor modulators
nAChRsTooltip Nicotinic acetylcholine receptors
Agonists
(and PAMsTooltip positive allosteric modulators)
Antagonists
(and NAMsTooltip negative allosteric modulators)
Precursors
(and prodrugs)
See also
Receptor/signaling modulators
Muscarinic acetylcholine receptor modulators
Acetylcholine metabolism/transport modulators
Categories:
Chlorfenvinphos Add topic