{"Abbreviation":["EPH"],"Aliases":["2-Piperidineacetic acid, α-phenyl-, ethyl ester","Dtxsid60912317","ethyl phenyl(2-piperidinyl)acetate","Dtxcid40842860","984DG861KD","Ethyl 2-phenyl-2-(piperidin-2-yl)acetate","ethyl phenyl(piperidin-2-yl)acetate","Chembl534479","Ethylphenidat","Methyl phenidate impurity E","Schembl727938","Chembl1187932","ZDA08855","Bdbm50165211","Akos025149438","FE31752","Methylphenidate Hydrochloride Impurity 12","DB-324101","NS00003758","C22752","α-Phenyl-2-piperidineacetic acid ethyl ester","Phenyl-piperidin-2-yl-acetic acid ethyl ester; hydrochloride","(2R,2''R)-Phenyl-piperidin-2-yl-acetic acid ethyl ester; hydrochloride","(2S,2''S)-Phenyl-piperidin-2-yl-acetic acid ethyl ester; hydrochloride"],"CAS":"57413-43-1","ChemicalClasses":["phenidate"],"Chirality":"racemic","Classes":["Stimulant"],"DBI-IGS":["Ethylphenidate"],"Dosing Info":[{"Method":"Oral","Tiers":{"Common":{"Entries":0,"Lower":42,"Percentage":0,"Unit":"mg","Upper":40},"Extreme":{"Entries":0,"Lower":75,"Percentage":0,"Unit":"mg","Upper":75},"Heavy":{"Entries":0,"Lower":75,"Percentage":0,"Unit":"mg","Upper":75},"Light":{"Entries":13,"Lower":42,"Percentage":54.2,"Unit":"mg","Upper":42},"Strong":{"Entries":11,"Lower":40,"Percentage":45.8,"Unit":"mg","Upper":75}}}],"Erowid Experience Reports":[{"Author":"Thbee","Id":104654,"Title":"Bad for Productive Purposes"},{"Author":"Billy Biscuits","Id":111467,"Title":"Long-Term Usage"},{"Author":"Fill","Id":103115,"Title":"Confident, Calm and Prosocial"},{"Author":"Hybrid213","Id":103109,"Title":"Is It Good When on My Own"},{"Author":"jamdonutta","Id":102515,"Title":"Very Cokey Edginess"},{"Author":"drb","Id":101470,"Title":"A Disappointing and Underwhelming First Time"},{"Author":"rawkingrukus","Id":101364,"Title":"Methyl vs Ethyl: What a Difference"},{"Author":"likuidpaper","Id":100914,"Title":"The Bomb"},{"Author":"Septum","Id":106244,"Title":"Corrosive and Addictive"},{"Author":"khyral","Id":99776,"Title":"Like Ketamine but With a Clearer Head"},{"Author":"mundungous","Id":99775,"Title":"One of My Favourite Highs"},{"Author":"dcal","Id":103226,"Title":"To My Dear Aunt Ethyl"},{"Author":"Patrick","Id":103656,"Title":"Two Weeks of Reporting"},{"Author":"Ockham","Id":106630,"Title":"Not Worth The Trouble"},{"Author":"Liddell","Id":106392,"Title":"Need Further Research"},{"Author":"thousandpoundbaby","Id":106312,"Title":"Surprise Addiction"},{"Author":"Crimsoncomq","Id":105973,"Title":"High Oral Dosage Multiple Days"},{"Author":"Redgenedge","Id":105483,"Title":"Painful Start but Potent and Pleasant"},{"Author":"Aspy","Id":104934,"Title":"Heaven and Hell"},{"Author":"Hunter","Id":104222,"Title":"Eight Hours of Periodically Dosing"},{"Author":"Almeeta","Id":103837,"Title":"So Very Variable"},{"Author":"Gigolo","Id":103713,"Title":"Reminds Me of Bad Quality Street Coke"},{"Author":"PseudoHuman","Id":99475,"Title":"Fun, Cheap and Potent"},{"Author":"phy","Id":99243,"Title":"An MDMAish, Lovely Time"},{"Author":"C15H21NO2","Id":99136,"Title":"The Positives and Negatives"},{"Author":"Bender","Id":96931,"Title":"Ritalin's Weaker Li'l Sis"}],"Esters":[],"Formating":[],"HMDB ID":"HMDB0252084","HeavyAtomCount":18,"IUPACName":"ethyl 2-phenyl-2-piperidin-2-ylacetate","InChI":"InChI=1S/C15H21NO2/c1-2-18-15(17)14(12-8-4-3-5-9-12)13-10-6-7-11-16-13/h3-5,8-9,13-14,16H,2,6-7,10-11H2,1H3","InChIKey":"AIVSIRYZIBXTMM-UHFFFAOYSA-N","MeSH Headers":[{"Id":"M0125225","Link":"https://id.nlm.nih.gov/mesh/M0125225.html","Name":"ethylphenidate","Ref":21},{"Id":"DescTree","Link":"https://www.nlm.nih.gov/mesh/meshhome.html","Name":"MeSH Tree","Ref":23},{"Id":"PubMed from MeSH","Link":"https://www.nlm.nih.gov/mesh/meshhome.html","Name":null,"Ref":34},{"Id":"M0001063","Link":"https://id.nlm.nih.gov/mesh/M0001063.html","Name":"Central Nervous System Stimulants","Ref":35},{"Id":"M0028095","Link":"https://id.nlm.nih.gov/mesh/M0028095.html","Name":"Adrenergic Uptake Inhibitors","Ref":36},{"Id":"M0028098","Link":"https://id.nlm.nih.gov/mesh/M0028098.html","Name":"Dopamine Uptake Inhibitors","Ref":37}],"MeSH Pharmacological Classification":[{"Id":"M0001063","Link":"https://id.nlm.nih.gov/mesh/M0001063.html","Name":"Central Nervous System Stimulant","Ref":35},{"Id":"M0028095","Link":"https://id.nlm.nih.gov/mesh/M0028095.html","Name":"Adrenergic Uptake Inhibitor","Ref":36},{"Id":"M0028098","Link":"https://id.nlm.nih.gov/mesh/M0028098.html","Name":"Dopamine Uptake Inhibitor","Ref":37}],"MolecularFormula":"C\u003csub\u003e15\u003c/sub\u003eH\u003csub\u003e21\u003c/sub\u003eNO\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"247.33 g/mol","PubChemId":3080846,"RefChem":"139196","RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Ethylphenidate","Name":"Ethylphenidate","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q5404506","Name":"Ethylphenidate","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/3080846","Name":"Ethylphenidate","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=57413-43-1","Name":"Ethylphenidate","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0252084","Name":"Ethylphenidate","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/C22752","Name":"Ethylphenidate","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID60912317","Name":"Ethylphenidate","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 3080846, Ethylphenidate. Accessed May 8, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/3080846\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/3080846\u003c/a\u003e","Anvisa. RDC Nº 804 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial. Diário Oficial da União. July 24, 2023. Accessed May 8, 2026. \u003ca href=https://www.in.gov.br/en/web/dou/-/resolucao-rdc-n-804-de-24-de-julho-de-2023-498447451\u003ehttps://www.in.gov.br/en/web/dou/-/resolucao-rdc-n-804-de-24-de-julho-de-2023-498447451\u003c/a\u003e"],"SMILES":"CCOC(=O)C(C1CCCCN1)C2=CC=CC=C2","SaltData":[],"Salts":[],"Scheduling":[{"gov":"Australia","ref":[],"schedule":"S8 (Controlled Drug) substance"},{"gov":"Brazil","ref":["2"],"schedule":"F2 substance"},{"gov":"Canada","ref":[],"schedule":"Schedule 3 substance"},{"gov":"United Kingdom","ref":[],"schedule":"Class B substance"},{"gov":"Germany","ref":[],"schedule":"Anlage II substance"},{"act":"Convention on Psychotropic Substances 1971","gov":"United Nations","ref":[],"schedule":"Schedule II drug"}],"StereoisomerData":[{"SMILES":"CCOC(=O)[C@@H](C1=CC=CC=C1)[C@@H]1CCCCN1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.29 78.285\"\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=\"#ff0d0d\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h82v79H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M14.25 1.038 27.447 8.66M27.447 8.66l-.002 11.319M30.72 25.792l9.921 5.73\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m40.641 31.522 9.919-5.724M40.642 28.707l8.699-5.021\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M50.56 25.798 45.6 28.66M49.341 23.686l-4.349 2.511\" class=\"hi\"/\u003e\u003c/g\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M40.289 46.762h.7M40.039 44.585h1.2M39.79 42.408h1.7M39.54 40.231h2.2M39.29 38.054h2.7M39.04 35.876l3.201.001M38.791 33.699l3.7.001M38.541 31.522l4.201.001\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.639 46.762-13.2 7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.439 54.38-13.201-7.63M25.001 55.787l-10.764-6.221\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.238 46.75-13.2 7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 54.368.003 15.248M3.477 55.776l.002 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.041 69.616 13.201 7.631\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.242 77.247 13.2-7.618M14.243 74.431l10.76-6.21\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.439 54.38.003 15.249M40.639 46.762l13.197 7.623M53.836 54.385v15.24M53.836 69.625l13.208 7.62M67.044 77.245l13.208-7.62M80.252 69.625v-15.24M80.252 54.385l-10.055-5.801\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"m53.661 54.081.35.607 10.72-4.647-.841-1.457-.84-1.457z\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M29.704 23.897q0 .756-.256 1.328-.256.565-.756.881-.501.315-1.245.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881t1.274-.316q.732 0 1.233.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.452M55.491 22.846q0 .756-.256 1.327-.256.566-.756.881t-1.245.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.566.756-.881t1.274-.316q.733 0 1.233.316.5.31.756.875.256.566.256 1.328m-3.864 0q0 .922.387 1.458.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.458 0-.929-.387-1.453-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.453\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.985 49.214h-.721l-2.619-4.066h-.03l.03.596q.024.357.024.732v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.768h.578zM68.848 43.753h-.619v-2.286h-2.513v2.286h-.613v-4.899h.613v2.071h2.513v-2.071h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m27.445 19.979.001-5.66M30.72 25.792l4.96 2.865\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.197 48.584 5.028 2.9M70.197 48.584l5.028 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(5S,6S)-Ethylphenidate"},{"SMILES":"CCOC(=O)[C@H](C1=CC=CC=C1)[C@@H]1CCCCN1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.29 78.285\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h82v79H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M14.25 1.038 27.447 8.66M27.447 8.66l-.002 11.319M30.72 25.792l9.921 5.73\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m40.641 31.522 9.919-5.724M40.642 28.707l8.699-5.021\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M50.56 25.798 45.6 28.66M49.341 23.686l-4.349 2.511\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M40.289 46.762h.7l1.902-16.538-2.25 1.298-2.249-1.299z\" class=\"bond\"/\u003e\u003cpath d=\"m40.639 46.762-13.2 7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.439 54.38-13.201-7.63M25.001 55.787l-10.764-6.221\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.238 46.75-13.2 7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 54.368.003 15.248M3.477 55.776l.002 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.041 69.616 13.201 7.631\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.242 77.247 13.2-7.618M14.243 74.431l10.76-6.21\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.439 54.38.003 15.249M40.639 46.762l13.197 7.623M53.836 54.385v15.24M53.836 69.625l13.208 7.62M67.044 77.245l13.208-7.62M80.252 69.625v-15.24M80.252 54.385l-10.055-5.801\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"m53.661 54.081.35.607 10.72-4.647-.841-1.457-.84-1.457z\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M29.704 23.897q0 .756-.256 1.328-.256.565-.756.881-.501.315-1.245.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881t1.274-.316q.732 0 1.233.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.452M55.491 22.846q0 .756-.256 1.327-.256.566-.756.881t-1.245.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.566.756-.881t1.274-.316q.733 0 1.233.316.5.31.756.875.256.566.256 1.328m-3.864 0q0 .922.387 1.458.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.458 0-.929-.387-1.453-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.453\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.985 49.214h-.721l-2.619-4.066h-.03l.03.596q.024.357.024.732v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.768h.578zM68.848 43.753h-.619v-2.286h-2.513v2.286h-.613v-4.899h.613v2.071h2.513v-2.071h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m27.445 19.979.001-5.66M30.72 25.792l4.96 2.865\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.197 48.584 5.028 2.9M70.197 48.584l5.028 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(5R,6S)-Ethylphenidate"},{"SMILES":"CCOC(=O)[C@@H](C1=CC=CC=C1)[C@H]1CCCCN1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.29 78.285\"\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=\"#ff0d0d\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h82v79H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M14.25 1.038 27.447 8.66M27.447 8.66l-.002 11.319M30.72 25.792l9.921 5.73\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m40.641 31.522 9.919-5.724M40.642 28.707l8.699-5.021\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M50.56 25.798 45.6 28.66M49.341 23.686l-4.349 2.511\" class=\"hi\"/\u003e\u003c/g\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M40.289 46.762h.7M40.039 44.585h1.2M39.79 42.408h1.7M39.54 40.231h2.2M39.29 38.054h2.7M39.04 35.876l3.201.001M38.791 33.699l3.7.001M38.541 31.522l4.201.001\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.639 46.762-13.2 7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.439 54.38-13.201-7.63M25.001 55.787l-10.764-6.221\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.238 46.75-13.2 7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 54.368.003 15.248M3.477 55.776l.002 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.041 69.616 13.201 7.631\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.242 77.247 13.2-7.618M14.243 74.431l10.76-6.21\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.439 54.38.003 15.249M40.639 46.762l13.197 7.623M53.836 54.385v15.24M53.836 69.625l13.208 7.62M67.044 77.245l13.208-7.62M80.252 69.625v-15.24M80.252 54.385l-10.055-5.801\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.661 54.081.35.607M55.423 52.776l.6 1.04M57.185 51.471l.849 1.473M58.947 50.166l1.099 1.906M60.709 48.861l1.349 2.339M62.471 47.556l1.599 2.772\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m62.058 51.2-.675-1.169M64.07 50.328l-.8-1.386M62.471 47.556l.799 1.386\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M29.704 23.897q0 .756-.256 1.328-.256.565-.756.881-.501.315-1.245.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881t1.274-.316q.732 0 1.233.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.452M55.491 22.846q0 .756-.256 1.327-.256.566-.756.881t-1.245.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.566.756-.881t1.274-.316q.733 0 1.233.316.5.31.756.875.256.566.256 1.328m-3.864 0q0 .922.387 1.458.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.458 0-.929-.387-1.453-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.453\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.985 49.214h-.721l-2.619-4.066h-.03l.03.596q.024.357.024.732v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.768h.578zM68.848 43.753h-.619v-2.286h-2.513v2.286h-.613v-4.899h.613v2.071h2.513v-2.071h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m27.445 19.979.001-5.66M30.72 25.792l4.96 2.865\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.197 48.584 5.028 2.9M70.197 48.584l5.028 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(5S,6R)-Ethylphenidate"},{"SMILES":"CCOC(=O)[C@H](C1=CC=CC=C1)[C@H]1CCCCN1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.29 78.285\"\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=\"#ff0d0d\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h82v79H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M14.25 1.038 27.447 8.66M27.447 8.66l-.002 11.319M30.72 25.792l9.921 5.73\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m40.641 31.522 9.919-5.724M40.642 28.707l8.699-5.021\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M50.56 25.798 45.6 28.66M49.341 23.686l-4.349 2.511\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"M40.289 46.762h.7l1.902-16.538-2.25 1.298-2.249-1.299z\" class=\"bond\"/\u003e\u003cpath d=\"m40.639 46.762-13.2 7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.439 54.38-13.201-7.63M25.001 55.787l-10.764-6.221\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.238 46.75-13.2 7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 54.368.003 15.248M3.477 55.776l.002 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.041 69.616 13.201 7.631\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.242 77.247 13.2-7.618M14.243 74.431l10.76-6.21\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.439 54.38.003 15.249M40.639 46.762l13.197 7.623M53.836 54.385v15.24M53.836 69.625l13.208 7.62M67.044 77.245l13.208-7.62M80.252 69.625v-15.24M80.252 54.385l-10.055-5.801\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.661 54.081.35.607M55.423 52.776l.6 1.04M57.185 51.471l.849 1.473M58.947 50.166l1.099 1.906M60.709 48.861l1.349 2.339M62.471 47.556l1.599 2.772\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m62.058 51.2-.675-1.169M64.07 50.328l-.8-1.386M62.471 47.556l.799 1.386\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M29.704 23.897q0 .756-.256 1.328-.256.565-.756.881-.501.315-1.245.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881t1.274-.316q.732 0 1.233.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.452M55.491 22.846q0 .756-.256 1.327-.256.566-.756.881t-1.245.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.566.756-.881t1.274-.316q.733 0 1.233.316.5.31.756.875.256.566.256 1.328m-3.864 0q0 .922.387 1.458.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.458 0-.929-.387-1.453-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.453\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.985 49.214h-.721l-2.619-4.066h-.03l.03.596q.024.357.024.732v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.768h.578zM68.848 43.753h-.619v-2.286h-2.513v2.286h-.613v-4.899h.613v2.071h2.513v-2.071h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m27.445 19.979.001-5.66M30.72 25.792l4.96 2.865\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.197 48.584 5.028 2.9M70.197 48.584l5.028 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(5R,6R)-Ethylphenidate"}],"StereoisomerType":"diastereomer","Stereoisomers":["(5S,6S)-Ethylphenidate","(5R,6S)-Ethylphenidate","(5S,6R)-Ethylphenidate","(5R,6R)-Ethylphenidate"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.29 78.285\"\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=\"#ff0d0d\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h82v79H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M14.25 1.038 27.447 8.66M27.447 8.66l-.002 11.319M30.72 25.792l9.921 5.73\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m39.422 30.818 10.528-6.076M40.641 32.93l10.528-6.076\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m49.95 24.742-5.264 3.038M51.169 26.854l-5.264 3.038\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.641 31.522-.002 15.24M40.639 46.762l13.197 7.623M53.836 54.385v15.24M53.836 69.625l13.208 7.62M67.044 77.245l13.208-7.62M80.252 69.625v-15.24M80.252 54.385l-10.055-5.801M53.836 54.385l10.054-5.801M40.639 46.762l-13.2 7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.439 54.38-13.201-7.63M25.001 55.787l-10.764-6.221\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.238 46.75-13.2 7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 54.368.003 15.248M3.477 55.776l.002 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.041 69.616 13.201 7.631\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.242 77.247 13.2-7.618M14.243 74.431l10.76-6.21\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.439 54.38.003 15.249\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M29.704 23.897q0 .756-.256 1.328-.256.565-.756.881-.501.315-1.245.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881t1.274-.316q.732 0 1.233.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.452M56.1 23.902q0 .756-.256 1.327-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.566.756-.881t1.274-.316q.732 0 1.232.316.5.309.756.875t.256 1.328m-3.864 0q0 .922.387 1.458.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.458 0-.929-.387-1.453-.381-.524-1.208-.524-.834 0-1.227.524t-.393 1.453\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.985 49.214h-.721l-2.619-4.066h-.03l.03.596q.024.357.024.732v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.768h.578zM68.848 43.753h-.619v-2.286h-2.513v2.286h-.613v-4.899h.613v2.071h2.513v-2.071h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m27.445 19.979.001-5.66M30.72 25.792l4.96 2.865\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.197 48.584 5.028 2.9M70.197 48.584l5.028 2.9M63.89 48.584l-5.027 2.9M63.89 48.584l-5.027 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":"Ethylphenidate","Wikidata":"Q5404506","Wikipedia":"Ethylphenidate","XLogP":0.6}