{"Abbreviation":"2-DPMP","Aliases":["Desoxypipradrol","2-Diphenylmethylpiperidine","2-DPMP","2-(Diphenylmethyl)piperidine","Deoxypipradol","Piperidine, 2-(diphenylmethyl)-","Desoxypipradol","Oprea1_652788","2-(Diphenylmethyl)piperidine; 2-Benzhydrylpiperidine","2-Diphenylmethyl-piperidine;2-DPMP","BBL020743","STK893433","LE-0263","A19451","A828867","208-276-6"],"Boiling Point":"150 °C","CAS":"519-74-4","ChemicalClasses":["phenidate"],"Chirality":"racemic","Classes":["Stimulant"],"Color/Form":"Orthrhombic from petroleum","EINECS":"208-276-6","EliminationHalfLife":"16 – 20 hours","Erowid Experience Reports":[{"Author":"HST","Id":"109229","Title":"Surprise Initiation"},{"Author":"AK139","Id":"98804","Title":"Do Not Recommend"}],"Esters":[],"European Community (EC) Number":"208-276-6","Formating":[],"HMDB ID":"HMDB0245105","HeavyAtomCount":19,"IUPACName":"2-benzhydrylpiperidine","InChI":"InChI=1S/C18H21N/c1-3-9-15(10-4-1)18(16-11-5-2-6-12-16)17-13-7-8-14-19-17/h1-6,9-12,17-19H,7-8,13-14H2","InChIKey":"RWTNXJXZVGHMGI-UHFFFAOYSA-N","Melting Point":"66 °C","MolecularFormula":"C\u003csub\u003e18\u003c/sub\u003eH\u003csub\u003e21\u003c/sub\u003eN","MolecularWeight":"251.4 g/mol","Opticalactivity":"( + / - )","PD":"PD048829","PubChemId":160506,"Record Description":["Wikipedia|List of designer drugs|Stimulants|Tropanes and Piperidines"],"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Desoxypipradrol","Name":"Desoxypipradrol","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q414480","Name":"Desoxypipradrol","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/160506","Name":"Desoxypipradrol","Sub":false}]},{"Name":"Probes \u0026 Drugs","Urls":[{"Link":"https://www.probes-drugs.org/compound/PD048829","Name":"Desoxypipradrol","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=519-74-4","Name":"Desoxypipradrol","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0245105","Name":"Desoxypipradrol","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/49UNK1BV8T","Name":"Desoxypipradrol","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID90897502","Name":"Desoxypipradrol","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 160506, Desoxypipradrol. Accessed July 13, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/160506\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/160506\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Desoxypipradrol. UNII: 49UNK1BV8T. Global Substance Registration System. Accessed July 13, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/49UNK1BV8T\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/49UNK1BV8T\u003c/a\u003e"],"SMILES":"C1CCNC(C1)C(C2=CC=CC=C2)C3=CC=CC=C3","SaltData":[],"Salts":[],"Scheduling":[{"gov":"Germany","ref":[],"schedule":"Anlage II substance"},{"gov":"United Kingdom","ref":[],"schedule":"Class B substance"}],"StereoisomerData":[{"Aliases":null,"PubChemId":null,"SMILES":"c1ccc(C(c2ccccc2)[C@H]2CCCCN2)cc1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.249 78.242\"\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 0h82v79H0z\"/\u003e\u003cg 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