{"Abbreviation":["α-PEA"],"Adverse Effects":"Dermatotoxin - Skin burns.","Aliases":["α-Methylbenzylamine","1-Phenylethanamine","1-Phenylethylamine","α-Phenylethylamine","1-Phenethylamine","α-Aminoethylbenzene","1-Amino-1-phenylethane","98-84-0","α-Methylbenzenemethanamine","α-Phenethylamine","Sumine 2079","Ethanamine, 1-phenyl-","Ethylamine, 1-phenyl-","(1-Aminoethyl)benzene","Benzene, (1-amino-ethyl)-","Benzylamine, α-methyl-","Benzenemethanamine, α-methyl-","Benzenemethaneamine, α-methyl-","202-706-6","210-545-8","618-36-0","1-phenylethan-1-amine","a-methylbenzylamine","1-Fenylethylamin","a-phenylethylamine"],"Boiling Point":"188.5 °C","CAS":"2627-86-3","ChEBI":"CHEBI:670","ChEMBL":"CHEMBL278059","ChemicalClasses":["α-alkylbenzylamine"],"Chirality":"racemic","Classes":["Monoamine oxidase inhibitor"],"Color/Form":"WATER-WHITE LIQ","Density":"0.9535 @ 20 °C/20 °C g/cm\u003csup\u003e3\u003c/sup\u003e","EINECS":"202-706-6","Esters":[],"European Community (EC) Number":"210-545-8","Flash Point":"79.4 °C","Formating":["alpha-methylbenzylamine"],"HMDB ID":"HMDB0002017","HeavyAtomCount":9,"IUPACName":"1-phenylethanamine","InChI":"InChI=1S/C8H11N/c1-7(9)8-5-3-2-4-6-8/h2-7H,9H2,1H3","InChIKey":"RQEUFEKYXDPUSK-UHFFFAOYSA-N","Interactions":"LINOLEIC ACID MIXED WITH ALPHA-METHYL BENZYLAMINE IN A 1:1 MOLAR RATIO \u0026 FED TO RATS, ON A HIGH CHOLESTEROL DIET, @ 0.2% OF THE DIET HAD NO EFFECT ON PLASMA \u0026 LIVER LIPID LEVELS.","LD50":[{"dosages":[{"amount":"940 mg/kg","route":"oral"}],"organism":"Rat"},{"dosages":[{"amount":"560 mg/kg","route":"oral"},{"amount":"240 mg/kg","route":"intraperitoneal"}],"organism":"Mouse"},{"dosages":[{"amount":"780 μL/kg","route":"skin"}],"organism":"Rabbit"}],"Melting Point":"-65 °C","MolecularFormula":"C\u003csub\u003e8\u003c/sub\u003eH\u003csub\u003e11\u003c/sub\u003eN","MolecularWeight":"121.18 g/mol","Odor":"MILD AMMONIACAL ODOR","Opticalactivity":"( + / - )","PD":"PD124031","Physical Description":"Liquid","PubChemId":7408,"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/1-Methylnaphthalene","Name":"α-Methylbenzylamine","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q3560549","Name":"α-Methylbenzylamine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/7408","Name":"α-Methylbenzylamine","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL278059","Name":"α-Methylbenzylamine","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:670","Name":"α-Methylbenzylamine","Sub":false}]},{"Name":"Probes \u0026 Drugs","Urls":[{"Link":"https://www.probes-drugs.org/compound/PD124031","Name":"α-Methylbenzylamine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=2627-86-3","Name":"α-Methylbenzylamine","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0002017","Name":"α-Methylbenzylamine","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/C02455","Name":"α-Methylbenzylamine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/HZ9DM6B2MT","Name":"α-Methylbenzylamine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID40862301","Name":"α-Methylbenzylamine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 7408, α-Methylbenzylamine. Accessed August 19, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/7408\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/7408\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. α-Methylbenzylamine. UNII: HZ9DM6B2MT. Global Substance Registration System. Accessed August 19, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/HZ9DM6B2MT\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/HZ9DM6B2MT\u003c/a\u003e"],"SMILES":"CC(C1=CC=CC=C1)N","SaltData":[{"AcidCount":1,"Amine":"α-Methylbenzylamine","AmineCount":1,"Formula":"Cl","Name":"hydrochloride","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 86.056 47.677\"\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 0h87v48H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M40.638.91v15.24M40.638 16.15 27.44 23.77\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.44 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