{"Abbreviation":"PEA","Aliases":["2-phenylethylamine","2-Phenylethanamine","2-Phenethylamine","β-Phenethylamine","1-Amino-2-phenylethane","β-Aminoethylbenzene","(2-Aminoethyl)benzene","1-Phenyl-2-aminoethane","2-Amino-1-phenylethane","Ethanamine, 2-phenyl-","Ethylamine, 2-phenyl-","1-Phenyl-2-amino-athan","2-Fenylethylamin","2-Amino-fenylethan","Phenethylamine, β","b-phenylethylamine","β-Phenylaethylamin","FEMA No. 3220","omega-Phenylethylamine","AI3-03117","Ec 200-574-4","1-Phenyl-2-amino-aethan","200-574-4","Benzeneethanamine","phenylethylamine"],"Biological Half-Life":"Plasma pharmacokinetics of PEA could be described by 1st-order kinetics with estimated t/2 of approx 5-10 min.","Boiling Point":"197.5 °C","CAS":"64-04-0","ChEBI":"CHEBI:18397","ChEMBL":"CHEMBL610","ChemicalClasses":["phenethylamine"],"Chirality":"achiral","Color/Form":"Colorless to slightly yellow liquid","Decomposition":"Hazardous decomposition products formed under fire conditions: Carbon oxides, nitrogen oxides (NOx).","Density":"0.9640 g/cu cm at 25 °C g/cm\u003csup\u003e3\u003c/sup\u003e","EINECS":"200-574-4","Erowid Experience Reports":null,"Esters":[],"European Community (EC) Number":"200-574-4","Flash Point":"81 °C (178 °F) - closed cup","Formating":[],"HMDB ID":"HMDB0012275","HeavyAtomCount":9,"IUPACName":"2-phenylethanamine","InChI":"InChI=1S/C8H11N/c9-7-6-8-4-2-1-3-5-8/h1-5H,6-7,9H2","InChIKey":"BHHGXPLMPWCGHP-UHFFFAOYSA-N","MeSH Pharmacological Classification":"A loosely defined grouping of drugs that have effects on psychological function. Here the psychotropic agents include the antidepressive agents, hallucinogens, and tranquilizing agents (including the antipsychotics and anti-anxiety agents). (See all compounds classified as Psychotropic Drugs.)","Melting Point":"\u003c0 °C","MolecularFormula":"C\u003csub\u003e8\u003c/sub\u003eH\u003csub\u003e11\u003c/sub\u003eN","MolecularWeight":"121.18 g/mol","Odor":"Fishy odor","Physical Description":"Liquid with a fishy odor; Absorbs carbon dioxide from the air; [Merck Index] Colorless liquid; [MSDSonline]","PubChemId":1001,"Record Description":["Wikipedia|PiHKAL|Phenethylamines"],"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Phenethylamine","Name":"Phenethylamine","Sub":false}]},{"Name":"DrugBank","Urls":[{"Link":"https://go.drugbank.com/drugs/DB04325","Name":"Phenethylamine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/1001","Name":"Phenethylamine","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL610","Name":"Phenethylamine","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:18397","Name":"Phenethylamine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=64-04-0","Name":"Phenethylamine","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0012275","Name":"Phenethylamine","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/C05332","Name":"Phenethylamine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/327C7L2BXQ","Name":"Phenethylamine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID5058773","Name":"Phenethylamine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 1001, Phenethylamine. Accessed July 17, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/1001\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/1001\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Phenethylamine. UNII: 327C7L2BXQ. Global Substance Registration System. Accessed July 17, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/327C7L2BXQ\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/327C7L2BXQ\u003c/a\u003e"],"SMILES":"C1=CC=C(C=C1)CCN","SaltData":[{"AcidCount":1,"AmineCount":1,"Formula":"Cl","Name":"hydrochloride","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 99.254 34.536\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg fill=\"#3050f8\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h100v35H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 10.621.005 15.249M3.477 12.029l.004 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.038 10.621 13.198-7.62\" 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class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"Phenethylamine","UNII":"327C7L2BXQ","Wikipedia":"Phenethylamine","XLogP":1.4,"pH":"Strong base"}