{"Abbreviation":"","Aliases":["VX nerve agent","VX agent","Phosphonothioic acid, methyl-, S-(2-(bis(1-methylethyl)amino)ethyl) O-ethyl ester","Phosphonothioic acid, P-methyl-, S-(2-(bis(1-methylethyl)amino)ethyl) O-ethyl ester","O-ethyl-S-[2-(N,N-diisopropylamino)ethyl] ester","O-Ethyl S-(2-diisopropylaminoethyl) methylthiophosphonate","S-{2-[di(propan-2-yl)amino]ethyl} O-ethyl methylphosphonothioate","Phosphonothioic acid, methyl-, S-[2-[bis(1-methylethyl)amino]ethyl] O-ethyl ester","O-ethyl-S-(2-(N,N-diisopropylamino)ethyl) ester","S-(2-(di(propan-2-yl)amino)ethyl) O-ethyl methylphosphonothioate"],"Boiling Point":"568 °","CAS":"50782-69-9","ChEBI":"CHEBI:136185","ChEMBL":"CHEMBL483105","ChemicalClasses":["alcohol"],"Chirality":"racemic","Classes":["Nerve agent"],"Color/Form":"Amber-colored liquid","Density":"1.0083 at 77 °F (EPA, 1998) - Denser than water; will sink g/cm\u003csup\u003e3\u003c/sup\u003e","DrugClasses":[],"Flash Point":"318.2 °F (EPA, 1998)","HMDB ID":"HMDB0259331","HeavyAtomCount":16,"IUPACName":"N-[2-[ethoxy(methyl)phosphoryl]sulfanylethyl]-N-propan-2-ylpropan-2-amine","InChI":"InChI=1S/C11H26NO2PS/c1-7-14-15(6,13)16-9-8-12(10(2)3)11(4)5/h10-11H,7-9H2,1-6H3","InChIKey":"JJIUCEJQJXNMHV-UHFFFAOYSA-N","MeSH Pharmacological Classification":"Drugs that inhibit cholinesterases. The neurotransmitter ACETYLCHOLINE is rapidly hydrolyzed, and thereby inactivated, by cholinesterases. When cholinesterases are inhibited, the action of endogenously released acetylcholine at cholinergic synapses is potentiated. Cholinesterase inhibitors are widely used clinically for their potentiation of cholinergic inputs to the gastrointestinal tract and urinary bladder, the eye, and skeletal muscles; they are also used for their effects on the heart and the central nervous system. (See all compounds classified as Cholinesterase Inhibitors.)","Melting Point":"Freezing point below -60 °F (EPA, 1998)","MolecularFormula":"C\u003csub\u003e11\u003c/sub\u003eH\u003csub\u003e26\u003c/sub\u003eNO\u003csub\u003e2\u003c/sub\u003ePS","MolecularWeight":"267.37 g/mol","Odor":"Odorless","Opticalactivity":"( + / - )","PD":"PD193129","Physical Description":"Phosphonothioic acid, methyl-, s-(2-(bis(1-methylethyl)amino)ethyl) o-ethyl ester appears as a chemical warfare nerve agent. Odorless liquid, with an amber color.","PrevSalts":[],"PubChemId":39793,"Record Description":["Phosphonothioic acid, methyl-, s-(2-(bis(1-methylethyl)amino)ethyl) o-ethyl ester appears as a chemical warfare nerve agent. Odorless liquid, with an amber color.","VX nerve agent is a organic thiophosphate that is the ethyl ester of S-{2-[di(propan-2-yl)amino]ethyl} O hydrogen methylphosphonothioate. A toxic nerve agent used in chemical warfare. It has a role as an EC 3.1.1.7 (acetylcholinesterase) inhibitor and a neurotoxin. It is an organic thiophosphate and a tertiary amino compound.","VX nerve agent is a organic thiophosphate that is the ethyl ester of S-{2-[di(propan-2-yl)amino]ethyl} O hydrogen methylphosphonothioate. A toxic nerve agent used in chemical warfare. It has a role as an EC 3.1.1.7 (acetylcholinesterase) inhibitor and a neurotoxin. It is an organic thiophosphate and a tertiary amino compound."],"RefCount":3,"References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/VX","Name":"VX","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q421809","Name":"VX","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/39793","Name":"VX","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL483105","Name":"VX","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:136185","Name":"VX","Sub":false}]},{"Name":"Probes \u0026 Drugs","Urls":[{"Link":"https://www.probes-drugs.org/compound/PD193129","Name":"VX","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=50782-69-9","Name":"VX","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0259331","Name":"VX","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/9A4381183B","Name":"VX","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID80866161","Name":"VX","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 39793, VX. Accessed June 22, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/39793\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/39793\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. VX. UNII: 9A4381183B. Global Substance Registration System. Accessed June 22, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/9A4381183B\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/9A4381183B\u003c/a\u003e"],"SMILES":"CCOP(=O)(C)SCCN(C(C)C)C(C)C","Solubility":"In water, 30 g/L at 25 °C","StereoisomerRacemic":"(RS)-VX","StoreUNII":["9A4381183B"],"StructureBase64":"<svg xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink" height="81.266mm" version="1.2" viewBox="0 0 101.136 81.266" width="101.136mm">
      
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