{"Abbreviation":[],"Actives":["Dextromethamphetamine","Dextroamphetamine"],"Aliases":["Benzphetamine","RefChem:1078733","Benzfetamine","benzphetamine","Benzphetaminw","N,α-Dimethyl-N-(phenylmethyl)benzeneethanamine","Benzeneethanamine, N,α-dimethyl-N-(phenylmethyl)-","N-Benzyl-N-methyl-1-phenyl-2-propanamine #","C07538","D07514","N-benzyl-n,α-dimethylphenethylamine","L000849","Q3322838","Phenethylamine, n-benzyl-n,α-dimethyl-","Phenethylamine, N-benzyl-N,α-dimethyl-, (+)-","Benzeneethanamine, n,α-dimethyl-n-(phenylmethyl)-","Benzeneethanamine, N,α-dimethyl-N-(phenylmethyl)-, (+)-"],"CAS":"101-47-3","ChemicalClasses":["N-benzylphenethylamine"],"Chirality":"racemic","Classes":["Prodrug","Stimulant"],"Esters":[],"Formating":[],"HMDB ID":"HMDB0250738","Health Effects":"Using large amounts of these drugs can result in a condition known as amphetamine psychosis -- which can result in auditory, visual and tactile hallucinations, intense paranoia, irrational thoughts and beliefs, delusions, and mental confusion.","HeavyAtomCount":18,"IUPACName":"N-benzyl-N-methyl-1-phenylpropan-2-amine","InChI":"InChI=1S/C17H21N/c1-15(13-16-9-5-3-6-10-16)18(2)14-17-11-7-4-8-12-17/h3-12,15H,13-14H2,1-2H3","InChIKey":"YXKTVDFXDRQTKV-UHFFFAOYSA-N","MolecularFormula":"C\u003csub\u003e17\u003c/sub\u003eH\u003csub\u003e21\u003c/sub\u003eN","MolecularWeight":"239.35 g/mol","Opticalactivity":"( + / - )","PubChemId":2341,"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Benzphetamine","Name":"Benzphetamine","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q100325978","Name":"Benzphetamine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/2341","Name":"Benzphetamine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=101-47-3","Name":"Benzphetamine","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0250738","Name":"Benzphetamine","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/C07538","Name":"Benzphetamine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/QZH832I91B","Name":"Benzphetamine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID50859308","Name":"Benzphetamine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 2341, Benzphetamine. Accessed October 6, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/2341\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/2341\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Benzphetamine. UNII: QZH832I91B. Global Substance Registration System. Accessed October 6, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/QZH832I91B\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/QZH832I91B\u003c/a\u003e"],"SMILES":"CC(CC1=CC=CC=C1)N(C)CC2=CC=CC=C2","SaltData":[{"AcidCount":1,"Amine":"Benzphetamine","AmineCount":1,"Formula":"Cl","Name":"hydrochloride","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 143.779 55.433\"\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=\"#1ff01f\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h144v56H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M53.836 46.767v-15.24M53.836 31.527l-13.198-7.62M40.638 23.907l-13.198 7.62\" class=\"bond\"/\u003e\u003cg 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8.667-13.203-7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m106.624 1.038-13.198 7.62M106.624 3.854l-10.759 6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m93.431 23.907-.005-15.249\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M68.975 26.356h-.72l-2.62-4.066h-.03l.03.596q.024.357.024.732v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.327-.024-.477q-.006-.262-.006-.482v-2.768h.578z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.881 25.727-5.023 2.9M67.034 20.057v-5.695M70.187 25.727l5.022 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Subjective Effects":{"Cognitive Effects":["Analysis enhancement","Ego inflation","Focus enhancement","Increased music appreciation","Motivation enhancement","Thought acceleration","Wakefulness","Disinhibition","Suggestibility suppression","Cognitive euphoria","Compulsive redosing","Mania"],"Physical Effects":["Increased libido","Stamina enhancement","Stimulation","Appetite suppression","Dehydration","Dry mouth","Restless legs","Shakiness","Teeth grinding","Abnormal heartbeat","Increased blood pressure","Increased heart rate","Vasoconstriction"],"Visual Effects":[]},"Title":"Benzphetamine","Toxicity Data":"LD50: 160 mg/kg (Oral, Rat) (A308)","Treatment":"Management of acute amphetamine intoxication is largely symptomatic and includes sedation with a barbiturate. If hypertension is marked, the use of a nitrite or rapidly acting alpha receptor blocking agent should be considered. Acidification of the urine increases amphetamine excretion. (L1712)","UNII":"QZH832I91B","Wikidata":"Q100325978","Wikipedia":"Benzphetamine","XLogP":4.1}