{"Abbreviation":"BA","Actives":["Amphetamine"],"Aliases":["N-n-butylamphetamine","51799-33-8","N-Butylamphetamine","1-Phenyl-2-butylaminopropane","1-Phenyl-2-n-butylamino-propan","n-butylamphetamine","Phenethylamine, N-butyl-α-methyl-","Benzeneethanamine, N-butyl-α-methyl-","4-12-00-02592","Ncgc00247329-01"],"CAS":"57378-21-9","ChEMBL":"CHEMBL1907545","ChemicalClasses":["amphetamine"],"Chirality":"racemic","Classes":["Stimulant","Prodrug"],"Erowid Experience Reports":null,"Esters":[],"Formating":[],"HeavyAtomCount":14,"IUPACName":"N-(1-phenylpropan-2-yl)butan-1-amine","InChI":"InChI=1S/C13H21N/c1-3-4-10-14-12(2)11-13-8-6-5-7-9-13/h5-9,12,14H,3-4,10-11H2,1-2H3","InChIKey":"VIAVBPFRYASSKF-UHFFFAOYSA-N","MolecularFormula":"C\u003csub\u003e13\u003c/sub\u003eH\u003csub\u003e21\u003c/sub\u003eN","MolecularWeight":"191.31 g/mol","PubChemId":94547,"RefCount":2,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Butylamphetamine","Name":"Butylamphetamine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/94547","Name":"Butylamphetamine","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1907545","Name":"Butylamphetamine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=57378-21-9","Name":"Butylamphetamine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID801024079","Name":"Butylamphetamine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 94547, Butylamphetamine. Accessed July 20, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/94547\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/94547\u003c/a\u003e"],"SMILES":"CCCCNC(C)CC1=CC=CC=C1","SaltData":[],"Salts":[],"StereoisomerData":[{"Aliases":null,"PubChemId":null,"SMILES":"CCCCN[C@H](C)Cc1ccccc1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 120.865 39.997\"\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 0h121v40H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m119.827 8.471-13.198 7.62M106.629 16.091l-13.198-7.62M93.431 8.471l-13.199 7.62M80.232 16.091l-10.045-5.8M63.881 10.291l-10.045 5.8\" class=\"bond\"/\u003e\u003cg 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4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483V6.021h.578zM68.838 5.459h-.619V3.173h-2.512v2.286h-.614V.56h.614v2.072h2.512V.56h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.187 10.291 5.022 2.9M70.187 10.291l5.022 2.9M63.881 10.291l-5.023 2.9M63.881 10.291l-5.023 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(R)-Butylamphetamine","UNII":null},{"Aliases":null,"PubChemId":null,"SMILES":"CCCCN[C@@H](C)Cc1ccccc1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 120.865 39.997\"\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 0h121v40H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m119.827 8.471-13.198 7.62M106.629 16.091l-13.198-7.62M93.431 8.471l-13.199 7.62M80.232 16.091l-10.045-5.8M63.881 10.291l-10.045 5.8\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"M54.186 16.091h-.7l-1.75 15.24h4.2z\" class=\"bond\"/\u003e\u003cpath d=\"m53.836 16.091-13.198-7.62M40.638 8.471l-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M27.44 16.091 14.236 8.462M25.002 17.498l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 8.462-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 16.082.005 15.249M3.477 17.49l.004 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 31.331 13.203 7.628\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.246 38.959 13.198-7.62M14.247 36.143l10.759-6.211\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 16.091.004 15.248\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.975 10.921h-.72l-2.62-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483V6.021h.578zM68.838 5.459h-.619V3.173h-2.512v2.286h-.614V.56h.614v2.072h2.512V.56h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.187 10.291 5.022 2.9M70.187 10.291l5.022 2.9M63.881 10.291l-5.023 2.9M63.881 10.291l-5.023 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(S)-Butylamphetamine","UNII":null}],"StereoisomerType":"enantiomer","Stereoisomers":["(R)-Butylamphetamine","(S)-Butylamphetamine"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 120.865 39.997\"\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 0h121v40H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m119.827 8.471-13.198 7.62M106.629 16.091l-13.198-7.62M93.431 8.471l-13.199 7.62M80.232 16.091l-10.045-5.8M63.881 10.291l-10.045 5.8M53.836 16.091v15.24M53.836 16.091l-13.198-7.62M40.638 8.471l-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M27.44 16.091 14.236 8.462M25.002 17.498l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 8.462-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 16.082.005 15.249M3.477 17.49l.004 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 31.331 13.203 7.628\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.246 38.959 13.198-7.62M14.247 36.143l10.759-6.211\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 16.091.004 15.248\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.975 10.921h-.72l-2.62-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483V6.021h.578zM68.838 5.459h-.619V3.173h-2.512v2.286h-.614V.56h.614v2.072h2.512V.56h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.187 10.291 5.022 2.9M70.187 10.291l5.022 2.9M63.881 10.291l-5.023 2.9M63.881 10.291l-5.023 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":"Butylamphetamine","Wikipedia":"Butylamphetamine","XLogP":3.4}
