TMPS

Impurity in malathion extremely toxic for mammals, structural isomer of TMP

General

Type : Organophosphate, Sulfur Compound

Chemical_Nomenclature : trimethoxy(sulfanylidene)-$l^{5}-phosphane

Canonical SMILES : COP(=S)(OC)OC

InChI : InChI=1S\/C3H9O3PS\/c1-4-7(8,5-2)6-3\/h1-3H3

InChIKey : XWSLYQXUTWUIKM-UHFFFAOYSA-N

Other name(s) : O,O,O-Trimethyl phosphorothioate, TMP=S, trimethoxy-sulfanylidene-phosphorane, Trimethyl thiophosphate, Trimethylthiophosphate, Trimethyl thionophosphate, O,O,O-Trimethylthiofosfat, Trimethoxyphosphine Sulfide, O,O,O-Trimethyl thiophosphate


MW : 156.142

Formula : C3H9O3PS

CAS_number : 152-18-1

PubChem : 9038

UniChem : XWSLYQXUTWUIKM-UHFFFAOYSA-N

Target

Families : TMPS ligand of proteins in family
ACHE

References (3)

Title : Synthesis and 31P chemical shift identification of tripeptide active site models that represent human serum acetylcholinesterase covalently modified at serine by certain organophosphates - Thompson_1996_Chem.Res.Toxicol_9_1325
Author(s) : Thompson CM , Suarez AI , Rodriguez OP
Ref : Chemical Research in Toxicology , 9 :1325 , 1996
PubMedID: 8951236

Title : Mutagenic and alkylating activities of organophosphate impurities of commercial malathion - Imamura_1985_Mutat.Res_155_1
Author(s) : Imamura T , Talcott RE
Ref : Mutat Res , 155 :1 , 1985
PubMedID: 3881662

Title : Toxicological properties of trialkyl phosphorothioate and dialkyl alkyl- and arylphosphonothioate esters - Fukuto_1983_J.Environ.Sci.Health.B_18_89
Author(s) : Fukuto TR
Ref : J Environ Sci Health B , 18 :89 , 1983
PubMedID: 6833715