{"Aliases":["α-Methylcyclopentaneethanamine","Dtxcid301736598","962-542-2","Schembl3901737","Schembl9213354","Schembl27689827","I+/--Methylcyclopentaneethanamine","2-cyclopentyl-1-methyl-ethylamine","AAA10523","AR-1K1985","Akos011598453","DB-338320","En300-332243","N12947"],"CAS":"105-23-7","ChemicalClasses":["cycloalkylamine"],"Chirality":"racemic","DTXSID":"501306640","DurationOfAction":"","EliminationHalfLife":"","Erowid Experience Reports":[],"Esters":[],"European Community (EC) Number":"962-542-2","Formating":[],"HeavyAtomCount":9,"IUPACName":"1-cyclopentylpropan-2-amine","InChI":"InChI=1S/C8H17N/c1-7(9)6-8-4-2-3-5-8/h7-8H,2-6,9H2,1H3","InChIKey":"JEJKKTYNUKTPTJ-UHFFFAOYSA-N","MeSH Headers":[],"MolecularFormula":"C\u003csub\u003e8\u003c/sub\u003eH\u003csub\u003e17\u003c/sub\u003eN","MolecularWeight":"127.23 g/mol","Opticalactivity":"( + / - )","PubChemId":7743,"PubChemTitle":"alpha-Methylcyclopentaneethanamine","Records":{"UNII":{"Impurities":[]}},"Reddit Experience Reports":[],"RefChem":"555873","RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Isocyclamine","Name":"Isocyclamine","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q27276667","Name":"Isocyclamine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/7743","Name":"Isocyclamine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=105-23-7","Name":"Isocyclamine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/DY4LH10D2X","Name":"Isocyclamine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID501306640","Name":"Isocyclamine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 7743, Isocyclamine. Accessed August 23, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/7743\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/7743\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Isocyclamine. UNII: DY4LH10D2X. Global Substance Registration System. Accessed August 23, 2026. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/DY4LH10D2X\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/DY4LH10D2X\u003c/a\u003e"],"SMILES":"CC(CC1CCCC1)N","SaltData":[],"Salts":[],"Scheduling":[],"StereoisomerData":[{"ChemicalClasses":["cycloalkylamine"],"SMILES":"C[C@@H](N)CC1CCCC1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 74.262 30.067\"\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=\".8\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h75v31H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M51.75 25.92V10.68\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m51.55 10.334.4.693M53.292 8.998l.686 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7.62M25.353 10.68 11.441 4.499M11.441 4.499 1.125 15.938M1.125 15.938l7.843 13.02M8.968 28.958 23.76 25.73M25.353 10.68 23.76 25.73\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M63.055.56h.911l2.214 4.185V.56h.661v5.001h-.911l-2.22-4.185v4.185h-.655zM67.413.56h.678v2.048h2.459V.56h.673v5.001h-.673V3.179h-2.459v2.382h-.678zM72.284 6.745h1.418v.343h-1.908v-.343q.232-.24.629-.64.4-.403.504-.521.196-.218.271-.368.079-.154.079-.3 0-.239-.168-.389t-.436-.15q-.193 0-.404.067-.21.065-.453.197v-.407q.246-.1.457-.15.214-.05.389-.05.468 0 .743.232.279.232.279.625 0 .182-.072.35-.068.164-.25.389-.05.057-.321.336-.268.279-.757.779\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(S)-Isocyclamine"}],"StereoisomerType":"enantiomer","Stereoisomers":["(R)-Isocyclamine","(S)-Isocyclamine"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 74.262 30.067\"\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=\".8\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h75v31H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M51.75 25.92V10.68M51.75 10.68 38.552 3.06M38.552 3.06l-13.199 7.62M25.353 10.68 11.441 4.499M11.441 4.499 1.125 15.938M1.125 15.938l7.843 13.02M8.968 28.958 23.76 25.73M25.353 10.68 23.76 25.73M51.75 10.68l9.919-5.727\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M63.055.56h.911l2.214 4.185V.56h.661v5.001h-.911l-2.22-4.185v4.185h-.655zM67.413.56h.678v2.048h2.459V.56h.673v5.001h-.673V3.179h-2.459v2.382h-.678zM72.284 6.745h1.418v.343h-1.908v-.343q.232-.24.629-.64.4-.403.504-.521.196-.218.271-.368.079-.154.079-.3 0-.239-.168-.389t-.436-.15q-.193 0-.404.067-.21.065-.453.197v-.407q.246-.1.457-.15.214-.05.389-.05.468 0 .743.232.279.232.279.625 0 .182-.072.35-.068.164-.25.389-.05.057-.321.336-.268.279-.757.779\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#3050f8\" d=\"m61.669 4.953-4.96 2.863M61.669 4.953l-4.96 2.863\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"Isocyclamine","UNII":"DY4LH10D2X","Wikidata":"Q27276667","Wikipedia":"Isocyclamine","XLogP":2.4}