{"Abbreviation":["IPH"],"Aliases":["Dtxsid001032294","Dtxcid701517300","Schembl12543306","NS00018221"],"CAS":"93148-46-0","ChemicalClasses":["phenidate"],"Chirality":"racemic","Classes":["Stimulant"],"DBI-IGS":["Isopropylphenidate"],"Dosing Info":[{"Method":"Insufflated","Tiers":{"Common":{"Entries":0,"Lower":50.9,"Percentage":0,"Unit":"mg","Upper":50},"Extreme":{"Entries":1,"Lower":66,"Percentage":33.3,"Unit":"mg","Upper":66},"Heavy":{"Entries":0,"Lower":60,"Percentage":0,"Unit":"mg","Upper":66},"Light":{"Entries":2,"Lower":50.9,"Percentage":66.7,"Unit":"mg","Upper":50.9},"Strong":{"Entries":0,"Lower":50,"Percentage":0,"Unit":"mg","Upper":60}}}],"Erowid Experience Reports":[{"Author":"Grapes","Id":111232,"Title":"One Month as a Daily Supplement"},{"Author":"Blank","Id":114647,"Title":"Energy for Everything Else but Actual Work"},{"Author":"wontofDA","Id":115578,"Title":"My Medicine"},{"Author":"Liber_Liebe_","Id":105594,"Title":"A Social Drug and a Nootropic"},{"Author":"MotivationNeeded","Id":108688,"Title":"It Starts Well but Doesn't Hold Up"},{"Author":"Zirtonic","Id":109186,"Title":"The Cleanest Stimulant I've Come Across"}],"Esters":[],"Formating":[],"HeavyAtomCount":19,"IUPACName":"propan-2-yl 2-phenyl-2-piperidin-2-ylacetate","InChI":"InChI=1S/C16H23NO2/c1-12(2)19-16(18)15(13-8-4-3-5-9-13)14-10-6-7-11-17-14/h3-5,8-9,12,14-15,17H,6-7,10-11H2,1-2H3","InChIKey":"AZVPADMEIMLODT-UHFFFAOYSA-N","MeSH Headers":[{"Id":"M000598569","Link":"https://id.nlm.nih.gov/mesh/M000598569.html","Name":"isopropylphenidate","Ref":10},{"Id":"DescTree","Link":"https://www.nlm.nih.gov/mesh/meshhome.html","Name":"MeSH Tree","Ref":12},{"Id":"PubMed from MeSH","Link":"https://www.nlm.nih.gov/mesh/meshhome.html","Name":null,"Ref":20}],"MolecularFormula":"C\u003csub\u003e16\u003c/sub\u003eH\u003csub\u003e23\u003c/sub\u003eNO\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"261.36 g/mol","PubChemId":68314762,"RefChem":"232058","RefCount":2,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Isopropylphenidate","Name":"Isopropylphenidate","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q21098898","Name":"Isopropylphenidate","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/68314762","Name":"Isopropylphenidate","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=93148-46-0","Name":"Isopropylphenidate","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID001032294","Name":"Isopropylphenidate","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 68314762, Isopropylphenidate. Accessed May 8, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/68314762\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/68314762\u003c/a\u003e"],"SMILES":"CC(C)OC(=O)C(C1CCCCN1)C2=CC=CC=C2","SaltData":[],"Salts":[],"Scheduling":[{"gov":"Canada","ref":[],"schedule":"Schedule III substance"},{"gov":"United Kingdom","ref":[],"schedule":"Class B substance"}],"StereoisomerData":[{"SMILES":"CC(C)OC(=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 8.66l13.199-7.618M27.447 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":"(6S,7S)-Isopropylphenidate"},{"SMILES":"CC(C)OC(=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 8.66l13.199-7.618M27.447 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":"(6R,7S)-Isopropylphenidate"},{"SMILES":"CC(C)OC(=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 8.66l13.199-7.618M27.447 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":"(6S,7R)-Isopropylphenidate"},{"SMILES":"CC(C)OC(=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 8.66l13.199-7.618M27.447 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":"(6R,7R)-Isopropylphenidate"}],"StereoisomerType":"diastereomer","Stereoisomers":["(6S,7S)-Isopropylphenidate","(6R,7S)-Isopropylphenidate","(6S,7R)-Isopropylphenidate","(6R,7R)-Isopropylphenidate"],"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 8.66l13.199-7.618M27.447 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":"Isopropylphenidate","Wikidata":"Q21098898","Wikipedia":"Isopropylphenidate","XLogP":1}