Phosphamidon

Phosphamidon
Names
IUPAC name
(E/Z)-[3-Chloro-4-(diethylamino)-4-oxobut-2-en-2-yl] dimethyl phosphate
Other names
Dimecron
Identifiers
CAS Number
  • 13171-21-6 checkY
  • 297-99-4 (E) checkY
  • 23783-98-4 (Z) checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 23990 ☒N
ECHA InfoCard 100.032.818 Edit this at Wikidata
KEGG
  • C18689 checkY
PubChem CID
  • 25750
UNII
  • 7H857A6N6H checkY
  • 54VR7A0BQD (E) checkY
  • HQ7958Q90Z (Z) checkY
CompTox Dashboard (EPA)
  • DTXSID7021156 Edit this at Wikidata
InChI
  • InChI=1S/C10H19ClNO5P/c1-6-12(7-2)10(13)9(11)8(3)17-18(14,15-4)16-5/h6-7H2,1-5H3 ☒N
    Key: RGCLLPNLLBQHPF-UHFFFAOYSA-N ☒N
  • InChI=1/C10H19ClNO5P/c1-6-12(7-2)10(13)9(11)8(3)17-18(14,15-4)16-5/h6-7H2,1-5H3
    Key: RGCLLPNLLBQHPF-UHFFFAOYAA
  • CCN(CC)C(=O)/C(=C(\C)/OP(=O)(OC)OC)/Cl
Properties
Chemical formula
C10H19ClNO5P
Molar mass 299.69 g·mol−1
Density 1.2132 g/cm3[1]
Melting point 120 to 123 °C (248 to 253 °F; 393 to 396 K)[3]
Boiling point 162 °C (324 °F; 435 K) (1.5 mmHg)[2]
Solubility in water
Miscible
Hazards
Lethal dose or concentration (LD, LC):
LD50 (median dose)
13 mg/kg (mouse, oral)[3]
6 mg/kg (mouse, IV)[3]
20 mg/kg (rat, oral)[3]
26 mg/kg (rat, subcut.)[3]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
Chemical compound

Phosphamidon is an organophosphate insecticide first reported in 1960.[3][2] It acts as a cholinesterase inhibitor.

The commercial product typically exists as a mixture of 70% (Z)-isomer and 30% (E)-isomer.[1]

Toxicity and regulation

Phosphamidon is very highly toxic to mammals and is listed as WHO Hazard Class Ia.[1] A harvester developed symptoms of moderately severe poisoning after working in a field that had been sprayed with the chemical 2 weeks earlier. He collapsed and exhibited significant depression of serum cholinesterase, but recovered completely within 2 days after successful treatment with atropine.[4] International trade of phosphamidon is covered by the Rotterdam Convention.

References

  1. ^ a b c Data Sheet on Pesticides No. 74: Phosphamidon, International Programme on Chemical Safety
  2. ^ a b Bachmann, Fritz (1960). "Phosphamidon, a new phosphate ester with systemic action". Proc. Intern. Cong. Crop. Protection, 4th Congr., Hamburg. 2: P1153-1155.
  3. ^ a b c d e f Jacques, R.; Bein, H. J. (1960). "Toxicology and pharmacology of a new systemic phosphoric acid ester insecticide phosphamidon (2-chloro-2-diethylcarbamoyl-1-methylvinyl dimethyl phosphate)". Archiv für Toxikologie. 18: 316–330. doi:10.1007/BF02226232. S2CID 6714997.
  4. ^ S. Gitelson, J. T. Davidson, A. Werczberger. Phosphamidon poisoning. Br. J. Ind. Med. 22: 236-239, 1965.
  • v
  • t
  • e
CarbamatesInorganic compoundsInsect growth regulatorsNeonicotinoidsOrganochloridesOrganophosphorusPyrethroidsRyanoidsOther chemicalsMetabolitesBiopesticides
  • v
  • t
  • e
Enzyme
(modulators)
ChATTooltip Choline acetyltransferase
  • Inhibitors: 1-(-Benzoylethyl)pyridinium
  • 2-(α-Naphthoyl)ethyltrimethylammonium
  • 3-Chloro-4-stillbazole
  • 4-(1-Naphthylvinyl)pyridine
  • Acetylseco hemicholinium-3
  • Acryloylcholine
  • AF64A
  • B115
  • BETA
  • CM-54,903
  • N,N-Dimethylaminoethylacrylate
  • N,N-Dimethylaminoethylchloroacetate
AChETooltip Acetylcholinesterase
BChETooltip Butyrylcholinesterase
Transporter
(modulators)
CHTTooltip Choline transporter
VAChTTooltip Vesicular acetylcholine transporter
Release
(modulators)
Inhibitors
  • SNAP-25Tooltip Synaptosomal-associated protein 25 inactivators: Botulinum toxin (A, C, E)
  • VAMPTooltip Vesicle-associated membrane protein inactivators: Botulinum toxin (B, D, F, G)
Enhancers
See also
Receptor/signaling modulators
Muscarinic acetylcholine receptor modulators
Nicotinic acetylcholine receptor modulators