{"Aliases":["Ephenidine","NEDPA","Benzeneethanamine, N-ethyl-α-phenyl-","Dtxsid601032416","n-ethyl-1,2-diphenylethanamine","Dtxcid801517422","N-Ethyl-α-phenylbenzeneethanamine","(1,2-Diphenylethyl)(ethyl)amine","n-ethyl-1,2-diphenylethylamine","Unii-ng69vg2948","Schembl5819528","Akos000206896","Phenethylamine, N-ethyl-α-phenyl-","N-ethyl-1,2-diphenylethan-1-amine","NS00018067","Benzeneethanamine, n-ethyl-α-phenyl-"],"CAS":"60951-19-1","ChemicalClasses":["1,2-diarylethylamine"],"Chirality":"racemic","EliminationHalfLife":"","Erowid Experience Reports":[{"Author":"nervewing","Id":108606,"Title":"The Electric Thrum"},{"Author":"Saubid","Id":109104,"Title":"A Fluid and Peaceful Happy Ending"},{"Author":"Xorkoth","Id":113483,"Title":"Pleasant, Then Unpleasant... A Likely Underdos"},{"Author":"UndercoverPunk","Id":108594,"Title":"Literally Life-Changing"},{"Author":"nervewing","Id":108460,"Title":"The Polychrome Sea"},{"Author":"Dimm","Id":107746,"Title":"Possibly Your Cup of Tea"},{"Author":"jackie","Id":107500,"Title":"Mild Calm Euphoria"},{"Author":"A","Id":112820,"Title":"Scattered Phase Almost Completely Goes Away"},{"Author":"Spartan","Id":106460,"Title":"Stimulation With Little Confusion"},{"Author":"The Quiet","Id":111988,"Title":"Multiday Mood Lift, Potentially Dangerous"},{"Author":"CdpDel","Id":111929,"Title":"Don't Know if It's My Addictive Personality..."},{"Author":"Student of Life","Id":110018,"Title":"The Lucid Dissociation - Warning Inside"},{"Author":"Student of Life","Id":109676,"Title":"Remember to Have Respect for Bliss"},{"Author":"Jezu","Id":106293,"Title":"A Night to Remember"},{"Author":"Anonymous","Id":107974,"Title":"A Couple's Experience"},{"Author":"InTPatrick","Id":106877,"Title":"Orgasmic Euphoria Submerged in Color"},{"Author":"Circadis","Id":113165,"Title":"Bliss and Clarity"},{"Author":"nervewing","Id":108612,"Title":"Tangle of Incomprehensible Rainbows"},{"Author":"jezu","Id":114251,"Title":"Almost Killed Me"}],"Esters":[],"Formating":[],"HeavyAtomCount":17,"IUPACName":"N-ethyl-1,2-diphenylethanamine","InChI":"InChI=1S/C16H19N/c1-2-17-16(15-11-7-4-8-12-15)13-14-9-5-3-6-10-14/h3-12,16-17H,2,13H2,1H3","InChIKey":"IGFZMQXEKIZPDR-UHFFFAOYSA-N","MeSH Headers":[{"Id":"M000634141","Link":"https://id.nlm.nih.gov/mesh/M000634141.html","Name":"ephenidine","Ref":14},{"Id":"DescTree","Link":"https://www.nlm.nih.gov/mesh/meshhome.html","Name":"MeSH Tree","Ref":16},{"Id":"PubMed from MeSH","Link":"https://www.nlm.nih.gov/mesh/meshhome.html","Name":null,"Ref":25}],"MolecularFormula":"C\u003csub\u003e16\u003c/sub\u003eH\u003csub\u003e19\u003c/sub\u003eN","MolecularWeight":"225.33 g/mol","Opticalactivity":"( + / - )","PubChemId":110821,"Record Description":["Ephenidine (also known as NEDPA and EPE) is a dissociative anesthetic that has been sold online as a designer drug.[1][2] It is illegal in some countries as a structural isomer of the banned opioid drug lefetamine, but has been sold in countries where it is not yet banned. Ephenidine and related diarylethylamines have been studied in vitro as treatments for neurotoxic injuries, and are antagonists of the NMDA receptor.","Wikipedia|List of designer drugs|Dissociatives|Diarylethylamines"],"Records":{"UNII":{"Impurities":[]}},"RefChem":"927149","RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Ephenidine","Name":"Ephenidine","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q20708135","Name":"Ephenidine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/110821","Name":"Ephenidine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=60951-19-1","Name":"Ephenidine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/NG69VG2948","Name":"Ephenidine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID601032416","Name":"Ephenidine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 110821, Ephenidine. Accessed May 6, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/110821\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/110821\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Ephenidine. UNII: NG69VG2948. Global Substance Registration System. Accessed May 6, 2026. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/NG69VG2948\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/NG69VG2948\u003c/a\u003e"],"SMILES":"CCNC(CC1=CC=CC=C1)C2=CC=CC=C2","SaltData":[],"Salts":[],"Scheduling":[{"gov":"Australia","ref":[],"schedule":"S9 substance"},{"gov":"Canada","ref":[],"schedule":"Schedule I substance"},{"act":"Neue-psychoaktive-Stoffe-Gesetz (NpSG)","gov":"Germany","ref":[],"schedule":"Neuer-Psychoaktiver-Stoff"},{"gov":"United Kingdom","ref":[],"schedule":"PSA substance"}],"StereoisomerData":[{"ChemicalClasses":["1,2-diarylethylamine"],"SMILES":"CCN[C@H](CC1=CC=CC=C1)C1=CC=CC=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 94.469 62.849\"\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\" 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