{"Abbreviation":"","Aliases":["Phenylethanolamine","2-Amino-1-phenylethanol","phenylethanolamine","Bisnorephedrine","2-Hydroxy-2-phenylethylamine","Phenethanolamine","2-Hydroxyphenethylamine","2-Phenyl-2-hydroxyethylamine","α-(Aminomethyl)benzyl alcohol","β-Hydroxyphenethylamine","2-amino-1-phenylethan-1-ol","β-Phenethanolamine","2-Amino-1-phenyl-1-ethanol","apophedrin","Ethanol, 2-amino-1-phenyl-","β-Hydroxy-β-phenylethylamine","α-Phenylglycinol","Benzenemethanol, α-(aminomethyl)-","Phenethylamine, β-hydroxy-","1-phenyl-2-aminoethanol","Benzeneethanamine, β-hydroxy-","β-Phenylethanolamine","Ethylamine, β-hydroxy-β-phenyl-","Benzyl alcohol, α-(aminomethyl)-","1-phenylethanolamine"],"CAS":"7568-93-6","ChEBI":"CHEBI:16343","ChEMBL":"CHEMBL19216","ChemicalClasses":["phenylethanolamine"],"Chirality":"racemic","Classes":["Sympathomimetic"],"EINECS":"231-469-1","Erowid Experience Reports":null,"Esters":[],"European Community (EC) Number":"231-469-1","Formating":[],"HMDB ID":"HMDB0001065","HeavyAtomCount":10,"IUPACName":"2-amino-1-phenylethanol","InChI":"InChI=1S/C8H11NO/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8,10H,6,9H2","InChIKey":"ULSIYEODSMZIPX-UHFFFAOYSA-N","Melting Point":"56.5 °C","MolecularFormula":"C\u003csub\u003e8\u003c/sub\u003eH\u003csub\u003e11\u003c/sub\u003eNO","MolecularWeight":"137.18 g/mol","Opticalactivity":"( + / - )","Physical Description":"Pale yellow solid; [Merck Index] Light yellow solidified mass or fragments; [Sigma-Aldrich MSDS]","PubChemId":1000,"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Inositol_nicotinate","Name":"Phenylethanolamine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/1000","Name":"Phenylethanolamine","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL19216","Name":"Phenylethanolamine","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:16343","Name":"Phenylethanolamine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=7568-93-6","Name":"Phenylethanolamine","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0001065","Name":"Phenylethanolamine","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/C02735","Name":"Phenylethanolamine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/2P4Y56479O","Name":"Phenylethanolamine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID10864094","Name":"Phenylethanolamine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 1000, Phenylethanolamine. Accessed July 15, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/1000\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/1000\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Phenylethanolamine. UNII: 2P4Y56479O. Global Substance Registration System. Accessed July 15, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/2P4Y56479O\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/2P4Y56479O\u003c/a\u003e"],"SMILES":"C1=CC=C(C=C1)C(CN)O","SaltData":[],"Salts":[],"Solubility":"45.8 mg/mL","StereoisomerData":[{"Aliases":null,"PubChemId":null,"SMILES":"NC[C@H](O)c1ccccc1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 76.346 49.848\"\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 0h77v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m63.881 20.142-10.045 5.799M53.836 25.941l-13.198-7.62\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" 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class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(S)-Phenylethanolamine","UNII":null}],"StereoisomerType":"enantiomer","Stereoisomers":["(R)-Phenylethanolamine","(S)-Phenylethanolamine"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 76.346 49.848\"\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 0h77v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 25.933.005 15.248M3.477 27.34l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.038 25.933 13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.44 25.941-13.204-7.628M25.002 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mouth","Restless legs","Shakiness","Abnormal heartbeat","Increased blood pressure","Increased heart rate","Vasoconstriction"],"Visual Effects":[]},"Title":"Phenylethanolamine","UNII":"2P4Y56479O","Wikipedia":"Inositol_nicotinate","XLogP":0.1}
