Propetamphos

General

Type : Organophosphate, Insecticide, Sulfur Compound

Chemical_Nomenclature : propan-2-yl (E)-3-[ethylamino(methoxy)phosphinothioyl]oxybut-2-enoate

Canonical SMILES : CCNP(=S)(OC)OC(=CC(=O)OC(C)C)C

InChI : InChI=1S\/C10H20NO4PS\/c1-6-11-16(17,13-5)15-9(4)7-10(12)14-8(2)3\/h7-8H,6H2,1-5H3,(H,11,17)\/b9-7+

InChIKey : BZNDWPRGXNILMS-VQHVLOKHSA-N

Other name(s) : 3-[(Ethylamino)methoxyphosphinothioyl]oxy]-2-butenoic acid,1-methylethyl ester, (E)-1-methylethyl 3-[{(ethylamino)methoxyphosphinothioly}oxy]-2-butenoate, Safrotin Zoecon, TSAR, Trade names for products containing propetamphos include Blotic, Safrotin and Seraphos. Commercial products include aerosols, emulsified concentrates, liquids, and powders


MW : 281.30

Formula : C10H20NO4PS

CAS_number : 31218-83-4

PubChem : 5372405

UniChem : BZNDWPRGXNILMS-VQHVLOKHSA-N

Target

Families : Propetamphos ligand of proteins in family
ACHE BCHE

References (2)

Title : Aging and spontaneous reactivation of human plasma cholinesterase activity after inhibition by organophosphorus pesticides - Mason_1993_Human.Exp.Toxicol_12_497
Author(s) : Mason HJ , Waine E , Stevenson A , Wilson HK
Ref : Hum Exp Toxicol , 12 :497 , 1993
PubMedID: 7904465

Title : Residual toxicity of wall-sprayed organophosphates, carbamates and pyrethroids to mosquito Culex pipiens molestus Forskal - Rettich_1980_J.Hyg.Epidemiol.Microbiol.Immunol_24_110
Author(s) : Rettich F
Ref : J Hyg Epidemiol Microbiol Immunol , 24 :110 , 1980
PubMedID: 7190586