{"Abbreviation":"","Aliases":["53214-57-6","2-(Methylamino)-1-phenyl-1-propanol","1-Ephedrine","Benzenemethanol, α-[1-(methylamino)ethyl]-","Benzyl alcohol, α-(1-methylaminoethyl)-","Ephedrine,(+)","Ephedrine","Pseudoephedrine,","1-α-(1-Methylaminoethyl)-benzyl alcohol","Benzenemethanol, [R-(R*,S*)]-","Wln: qyr \u0026 y1 \u0026 m1","α-(1-Methylaminoethyl)benzyl alcohol","α-Hydroxy-β-methyl amine propylbenzene","(1R,2S)-(-)-ephedrine","Spectrum2_001309","Spectrum3_000563","Spectrum4_000497","Spectrum5_001106","Benzenemethanol, α-(1-(methylamino)ethyl)-","1R, 2S (-)-Ephedrine","Oprea1_287330","BSPBio_001946","Ephedrine, (.+/-.)-","KBioGR_001013","Wln: qyr\u0026y1\u0026m1"],"CAS":"90-82-4","ChEMBL":"CHEMBL279157","ChemicalClasses":["phenylethanolamine"],"Chirality":"racemic","Classes":["Stimulant"],"Erowid Experience Reports":[],"Esters":[],"Formating":["beta-hydroxymethamphetamine"],"HMDB ID":"HMDB0246924","HeavyAtomCount":12,"IUPACName":"2-(methylamino)-1-phenylpropan-1-ol","InChI":"InChI=1S/C10H15NO/c1-8(11-2)10(12)9-6-4-3-5-7-9/h3-8,10-12H,1-2H3","InChIKey":"KWGRBVOPPLSCSI-UHFFFAOYSA-N","MolecularFormula":"C\u003csub\u003e10\u003c/sub\u003eH\u003csub\u003e15\u003c/sub\u003eNO","MolecularWeight":"165.23 g/mol","PubChemId":5032,"RefCount":2,"RefCur":"","References":[{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q105146923","Name":"β-Hydroxymethamphetamine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/5032","Name":"β-Hydroxymethamphetamine","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL279157","Name":"β-Hydroxymethamphetamine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=90-82-4","Name":"β-Hydroxymethamphetamine","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0246924","Name":"β-Hydroxymethamphetamine","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/C22822","Name":"β-Hydroxymethamphetamine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID70858959","Name":"β-Hydroxymethamphetamine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 5032, β-Hydroxymethamphetamine. Accessed July 13, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/5032\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/5032\u003c/a\u003e"],"SMILES":"CC(C(C1=CC=CC=C1)O)NC","SaltData":[],"Salts":[],"StereoisomerData":[{"Aliases":null,"PubChemId":null,"SMILES":"CN[C@H](C)[C@@H](O)c1ccccc1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.271 49.848\"\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 0h82v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m80.232 25.941-10.045-5.799M63.881 20.142l-10.045 5.799\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M54.186 25.941h-.7M54.436 28.118h-1.2M54.686 30.295h-1.7M54.936 32.473h-2.2M55.186 34.65h-2.7M55.436 36.827h-3.2M55.686 39.004h-3.7M55.936 41.181h-4.2\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.836 25.941-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M40.288 18.321h.7\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M40.038 16.144h1.2M39.788 13.967h1.7M39.538 11.79h2.2M39.288 9.613h2.7M39.038 7.435h3.2\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.638 18.321-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.44 25.941-13.204-7.628M25.002 27.349l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 18.313-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 25.933.005 15.248M3.477 27.34l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 41.181 13.203 7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.246 48.81 13.198-7.62M14.247 45.994l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 25.941.004 15.249\" class=\"bond\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.975 20.771h-.72l-2.62-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.055h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.769h.578zM68.838 15.31h-.619v-2.286h-2.512v2.286h-.614v-4.9h.614v2.072h2.512V10.41h.619z\"/\u003e\u003c/g\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M42.897 3.078q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881T40.653.56q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.393.523-.393 1.452M47.203 5.531h-.619V3.245h-2.512v2.286h-.613v-4.9h.613v2.072h2.512V.631h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.187 20.142 5.022 2.899M70.187 20.142l5.022 2.899M63.881 20.142l-5.023 2.899M63.881 20.142l-5.023 2.899\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"Ephedrine","UNII":null},{"Aliases":null,"PubChemId":null,"SMILES":"CN[C@@H](C)[C@@H](O)c1ccccc1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.271 49.848\"\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 0h82v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m80.232 25.941-10.045-5.799M63.881 20.142l-10.045 5.799\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"M54.186 25.941h-.7l-1.75 15.24h4.2z\" class=\"bond\"/\u003e\u003cpath d=\"m53.836 25.941-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M40.288 18.321h.7\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M40.038 16.144h1.2M39.788 13.967h1.7M39.538 11.79h2.2M39.288 9.613h2.7M39.038 7.435h3.2\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.638 18.321-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.44 25.941-13.204-7.628M25.002 27.349l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 18.313-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 25.933.005 15.248M3.477 27.34l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 41.181 13.203 7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.246 48.81 13.198-7.62M14.247 45.994l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 25.941.004 15.249\" class=\"bond\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.975 20.771h-.72l-2.62-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.055h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.769h.578zM68.838 15.31h-.619v-2.286h-2.512v2.286h-.614v-4.9h.614v2.072h2.512V10.41h.619z\"/\u003e\u003c/g\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M42.897 3.078q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881T40.653.56q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.393.523-.393 1.452M47.203 5.531h-.619V3.245h-2.512v2.286h-.613v-4.9h.613v2.072h2.512V.631h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.187 20.142 5.022 2.899M70.187 20.142l5.022 2.899M63.881 20.142l-5.023 2.899M63.881 20.142l-5.023 2.899\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"Pseudoephedrine","UNII":null},{"Aliases":null,"PubChemId":null,"SMILES":"CN[C@H](C)[C@H](O)c1ccccc1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.271 49.848\"\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 0h82v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m80.232 25.941-10.045-5.799M63.881 20.142l-10.045 5.799\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M54.186 25.941h-.7M54.436 28.118h-1.2M54.686 30.295h-1.7M54.936 32.473h-2.2M55.186 34.65h-2.7M55.436 36.827h-3.2M55.686 39.004h-3.7M55.936 41.181h-4.2\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.836 25.941-13.198-7.62\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"M40.288 18.321h.7l1.3-11.319h-3.3z\" class=\"bond\"/\u003e\u003cpath d=\"m40.638 18.321-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.44 25.941-13.204-7.628M25.002 27.349l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 18.313-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 25.933.005 15.248M3.477 27.34l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 41.181 13.203 7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.246 48.81 13.198-7.62M14.247 45.994l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 25.941.004 15.249\" class=\"bond\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.975 20.771h-.72l-2.62-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.055h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.769h.578zM68.838 15.31h-.619v-2.286h-2.512v2.286h-.614v-4.9h.614v2.072h2.512V10.41h.619z\"/\u003e\u003c/g\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M42.897 3.078q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881T40.653.56q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.393.523-.393 1.452M47.203 5.531h-.619V3.245h-2.512v2.286h-.613v-4.9h.613v2.072h2.512V.631h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.187 20.142 5.022 2.899M70.187 20.142l5.022 2.899M63.881 20.142l-5.023 2.899M63.881 20.142l-5.023 2.899\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(1R,2R)-β-Hydroxymethamphetamine","UNII":null},{"Aliases":null,"PubChemId":null,"SMILES":"CN[C@@H](C)[C@H](O)c1ccccc1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.271 49.848\"\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 0h82v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m80.232 25.941-10.045-5.799M63.881 20.142l-10.045 5.799\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M54.186 25.941h-.7l-1.75 15.24h4.2z\" class=\"bond\"/\u003e\u003cpath d=\"m53.836 25.941-13.198-7.62\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M40.288 18.321h.7l1.3-11.319h-3.3z\" class=\"bond\"/\u003e\u003cpath d=\"m40.638 18.321-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.44 25.941-13.204-7.628M25.002 27.349l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 18.313-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 25.933.005 15.248M3.477 27.34l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 41.181 13.203 7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.246 48.81 13.198-7.62M14.247 45.994l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 25.941.004 15.249\" class=\"bond\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.975 20.771h-.72l-2.62-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.055h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.769h.578zM68.838 15.31h-.619v-2.286h-2.512v2.286h-.614v-4.9h.614v2.072h2.512V10.41h.619z\"/\u003e\u003c/g\u003e\u003cg fill=\"#ff0d0d\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M42.897 3.078q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881T40.653.56q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.393.523-.393 1.452M47.203 5.531h-.619V3.245h-2.512v2.286h-.613v-4.9h.613v2.072h2.512V.631h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.187 20.142 5.022 2.899M70.187 20.142l5.022 2.899M63.881 20.142l-5.023 2.899M63.881 20.142l-5.023 2.899\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(1S,2R)-β-Hydroxymethamphetamine","UNII":null}],"StereoisomerType":"diastereomer","Stereoisomers":["Ephedrine","Pseudoephedrine","(1R,2R)-β-Hydroxymethamphetamine","(1S,2R)-β-Hydroxymethamphetamine"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.271 49.848\"\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 0h82v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M53.836 41.181v-15.24M53.836 25.941l-13.198-7.62M40.638 18.321l-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.44 25.941-13.204-7.628M25.002 27.349l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 18.313-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 25.933.005 15.248M3.477 27.34l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 41.181 13.203 7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.246 48.81 13.198-7.62M14.247 45.994l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 25.941.004 15.249M40.638 18.321V7.002M53.836 25.941l10.045-5.799M70.187 20.142l10.045 5.799\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M42.897 3.078q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881T40.653.56q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.393.523-.393 1.452M47.203 5.531h-.619V3.245h-2.512v2.286h-.613v-4.9h.613v2.072h2.512V.631h.619z\"/\u003e\u003c/g\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.975 20.771h-.72l-2.62-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.055h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.769h.578zM68.838 15.31h-.619v-2.286h-2.512v2.286h-.614v-4.9h.614v2.072h2.512V10.41h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M40.638 7.002v5.66M40.638 7.002v5.66\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.881 20.142-5.023 2.899M63.881 20.142l-5.023 2.899M70.187 20.142l5.022 2.899M70.187 20.142l5.022 2.899\" 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":"β-Hydroxymethamphetamine","Wikidata":"Q105146923","XLogP":0.9}