{"Abbreviation":["2C-B"],"Aliases":["4-Bromo-2,5-dimethoxyphenethylamine","2-(4-Bromo-2,5-dimethoxyphenyl)ethylamine","2-(4-Bromo-2,5-dimethoxyphenyl)ethanamine","4-Bromo-2,5-dimethoxyphenylethylamine","Benzeneethanamine, 4-bromo-2,5-dimethoxy-","2C-B","Nexus","BDMPEA","2-CB","4-Bromo-2,5-dimethoxybenzeneethanamine","4-Bromo-2,5dimethoxyphenethylamine","α-Desmethyl dob","GTPL13549","Bromo-2,5-dimethoxyphenylethylamine","Pdsp1_001367","Pdsp2_001351","DB01537","Ncgc00168259-01","MFT","J456.895H","2-(4-bromanyl-2,5-dimethoxy-phenyl)ethanamine","2-(4-bromo-2,5-dimethoxy-phenyl)-ethyl-amine","2-(4-Bromo-2,5-dimethoxy-phenyl)-ethylamine","2-(4-Bromo-2,5-dimethoxyphenyl)ethanamine #","C22775"],"CAS":"66142-81-2","ChEBI":"CHEBI:189669","ChEMBL":"CHEMBL292821","ChemicalClasses":["2,5-dimethoxyphenethylamine"],"Chirality":"achiral","Classes":["Psychedelic"],"DBI-IGS":["2C-B"],"DEA no":7392,"Dosing Info":[{"Method":"Insufflated","Tiers":{"Common":{"Entries":20,"Lower":8.3,"Percentage":34.5,"Unit":"mg","Upper":10},"Extreme":{"Entries":6,"Lower":17.3,"Percentage":10.3,"Unit":"mg","Upper":17.3},"Heavy":{"Entries":9,"Lower":13.8,"Percentage":15.5,"Unit":"mg","Upper":17.3},"Light":{"Entries":21,"Lower":8.3,"Percentage":36.2,"Unit":"mg","Upper":8.3},"Strong":{"Entries":2,"Lower":10,"Percentage":3.4,"Unit":"mg","Upper":13.8}}},{"Method":"Oral","Tiers":{"Common":{"Entries":3,"Lower":17,"Percentage":21.4,"Unit":"mg","Upper":21},"Extreme":{"Entries":2,"Lower":34.4,"Percentage":14.3,"Unit":"mg","Upper":34.4},"Heavy":{"Entries":1,"Lower":25,"Percentage":7.1,"Unit":"mg","Upper":34.4},"Light":{"Entries":4,"Lower":17,"Percentage":28.6,"Unit":"mg","Upper":17},"Strong":{"Entries":4,"Lower":21,"Percentage":28.6,"Unit":"mg","Upper":25}}},{"Method":"Intrarectal","Tiers":{"Common":{"Entries":0,"Lower":12.4,"Percentage":0,"Unit":"mg","Upper":13.5},"Extreme":{"Entries":2,"Lower":24,"Percentage":16.7,"Unit":"mg","Upper":24},"Heavy":{"Entries":0,"Lower":20,"Percentage":0,"Unit":"mg","Upper":24},"Light":{"Entries":6,"Lower":12.4,"Percentage":50,"Unit":"mg","Upper":12.4},"Strong":{"Entries":4,"Lower":13.5,"Percentage":33.3,"Unit":"mg","Upper":20}}}],"DurationOfAction":"Oral: 2 – 8 hours\u003ca href='#cite_note-5'\u003e\u003csup\u003e[5]\u003c/sup\u003e\u003c/a\u003e","EliminationHalfLife":"1.2 – 2.5 hours\u003ca href='#cite_note-3'\u003e\u003csup\u003e[3]\u003c/sup\u003e\u003c/a\u003e\u003ca href='#cite_note-4'\u003e\u003csup\u003e[4]\u003c/sup\u003e\u003c/a\u003e","Esters":[],"European Community (EC) Number":"636-275-4","Formating":[],"HeavyAtomCount":14,"IUPACName":"2-(4-bromo-2,5-dimethoxyphenyl)ethanamine","InChI":"InChI=1S/C10H14BrNO2/c1-13-9-6-8(11)10(14-2)5-7(9)3-4-12/h5-6H,3-4,12H2,1-2H3","InChIKey":"YMHOBZXQZVXHBM-UHFFFAOYSA-N","MeSH Pharmacological Classification":"Endogenous compounds and drugs that specifically stimulate SEROTONIN 5-HT2 RECEPTORS. Included under this heading are agonists for one or more of the specific 5-HT2 receptor subtypes.","MolecularFormula":"C\u003csub\u003e10\u003c/sub\u003eH\u003csub\u003e14\u003c/sub\u003eBrNO\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"260.13 g/mol","PD":"PD008796","PubChemId":98527,"Record Description":["Wikipedia|PiHKAL|Phenethylamines","Wikipedia|List of designer drugs|Psychedelics|2C-x (2,5-dimethoxy-phenethylamine derivatives)"],"RefChem":"82888","RefCount":6,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/2C-B","Name":"2,5-Dimethoxy-4-bromophenethylamine","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q229942","Name":"2,5-Dimethoxy-4-bromophenethylamine","Sub":false}]},{"Name":"DrugBank","Urls":[{"Link":"https://go.drugbank.com/drugs/DB01537","Name":"2,5-Dimethoxy-4-bromophenethylamine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/98527","Name":"2,5-Dimethoxy-4-bromophenethylamine","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL292821","Name":"2,5-Dimethoxy-4-bromophenethylamine","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:189669","Name":"2,5-Dimethoxy-4-bromophenethylamine","Sub":false}]},{"Name":"Probes \u0026 Drugs","Urls":[{"Link":"https://www.probes-drugs.org/compound/PD008796","Name":"2,5-Dimethoxy-4-bromophenethylamine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=66142-81-2","Name":"2,5-Dimethoxy-4-bromophenethylamine","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/C22775","Name":"2,5-Dimethoxy-4-bromophenethylamine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/V77772N32H","Name":"2,5-Dimethoxy-4-bromophenethylamine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID10216332","Name":"2,5-Dimethoxy-4-bromophenethylamine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 98527, 2,5-Dimethoxy-4-bromophenethylamine. Accessed October 14, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/98527\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/98527\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-4-bromophenethylamine. UNII: V77772N32H. Global Substance Registration System. Accessed October 14, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/V77772N32H\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/V77772N32H\u003c/a\u003e","Papaseit E, Farré M, Pérez-Mañá C, Torrens M, Ventura M, Pujadas M, de la Torre R, González D. Acute Pharmacological Effects of 2C-B in Humans: An Observational Study. Frontiers in Pharmacology. 2018; 9","Thomann J, Rudin D, Kraus S, Arikci D, Holze F, Liechti ME, Luethi D. LC–MS/MS-based pharmacokinetic and metabolic analysis of 4-bromo-2,5-dimethoxyphenethylamine (2C-B) and its metabolites in human plasma. Drug Metabolism and Disposition. 2025; 53(6)","Inan F, Brunt TM, Contrucci RR, Hondebrink L, Franssen EJ. Novel Phenethylamines and Their Potential Interactions With Prescription Drugs: A Systematic Critical Review. Ther Drug Monit. April 1, 2020; 42(2):271–281."],"SMILES":"COC1=CC(=C(C=C1CCN)OC)Br","SaltData":[{"AcidCount":1,"Amine":"2,5-Dimethoxy-4-bromophenethylamine","AmineCount":1,"Formula":"Cl","Name":"hydrochloride","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 117.432 78.276\"\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 0h118v79H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m19.213 1.038 9.914 5.724M32.411 12.579v11.319\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m32.411 23.898-13.208 7.62M32.411 26.713l-10.77 6.214\"/\u003e\u003c/g\u003e\u003cpath d=\"M19.203 31.518v15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m19.203 46.758 13.208 7.62M21.641 45.35l10.77 6.213\"/\u003e\u003c/g\u003e\u003cpath d=\"m32.411 54.378 13.208-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M45.619 46.758v-15.24M43.18 45.35V32.927\"/\u003e\u003c/g\u003e\u003cpath d=\"m32.411 23.898 13.208 7.62M45.619 31.518l13.197-7.622M58.816 23.896l13.199 7.618M72.015 31.514l10.044-5.801M32.411 54.378v11.319M35.686 71.509l9.923 5.729M19.203 46.758 7.771 53.361\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M34.67 8.655q0 .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-.881t1.274-.316q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.863 0q0 .923.386 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.392.524-.392 1.452\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M87.153 26.342h-.72l-2.62-4.066h-.029l.029.595q.024.357.024.732v2.739h-.565v-4.9h.714l2.607 4.054h.03l-.018-.327q-.012-.22-.023-.476-.006-.262-.006-.483v-2.768h.577zM91.459 26.342h-.619v-2.286h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.619zM93.964 27.831h-1.943v-.3l.771-.779q.222-.221.372-.393.154-.175.232-.339.079-.168.079-.364 0-.243-.147-.368-.143-.129-.371-.129-.215 0-.379.075-.161.075-.328.207l-.193-.242q.171-.147.393-.247.225-.1.507-.1.411 0 .65.207t.239.575q0 .229-.096.433-.093.2-.265.396-.167.196-.392.418l-.615.604v.017h1.486z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M34.67 69.615q0 .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-.881t1.274-.316q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.863 0q0 .923.386 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.392.524-.392 1.452\" class=\"atom\"/\u003e\u003cpath fill=\"#a62929\" stroke=\"none\" d=\"M1.959 51.353q.917 0 1.387.274.47.268.47.941 0 .434-.244.72-.238.286-.69.363v.036q.309.047.559.178t.393.375q.149.239.149.62 0 .666-.458 1.029-.459.364-1.245.364H.56v-4.9zm.119 2.09q.631 0 .863-.203.238-.202.238-.601 0-.405-.285-.577-.286-.179-.911-.179h-.81v1.56zm-.905.512v1.774h.988q.655 0 .905-.25.256-.256.256-.667 0-.381-.268-.619-.262-.238-.94-.238zm5.476-1.447q.101 0 .22.012.125.006.208.03l-.071.553q-.089-.018-.196-.029-.108-.018-.203-.018-.28 0-.53.154-.244.155-.393.435-.148.274-.148.649v1.959h-.602v-3.674h.494l.066.667h.03q.178-.297.458-.518.28-.22.667-.22\" class=\"atom\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M29.127 6.762 24.17 3.9M32.411 12.579v5.66\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m82.059 25.713-5.022 2.901\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M32.411 65.697v-5.659M35.686 71.509l4.962 2.865\" class=\"hi\"/\u003e\u003cpath stroke=\"#a62929\" d=\"m7.771 53.361 5.716-3.302\" class=\"hi\"/\u003e\u003c/g\u003e\u003cg class=\"mol\"\u003e\u003cg fill=\"#1ff01f\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M114.116 37.287q-.786 0-1.238.53-.453.523-.453 1.446 0 .911.417 1.447.422.53 1.268.53.321 0 .607-.054.292-.059.566-.143v.536q-.274.101-.566.149-.292.053-.696.053-.745 0-1.251-.309-.5-.31-.75-.875-.25-.572-.25-1.34 0-.744.268-1.309.274-.566.804-.882.53-.321 1.28-.321.78 0 1.351.286l-.244.524q-.226-.102-.506-.185-.274-.083-.607-.083m2.756 4.423h-.601v-5.215h.601zM111.209 41.71h-.62v-2.286h-2.512v2.286h-.613v-4.9h.613v2.072h2.512V36.81h.62z\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"2,5-Dimethoxy-4-bromophenethylamine hydrochloride","UNII":"6AVT4WPN6M"},{"AcidCount":1,"Amine":"2,5-Dimethoxy-4-bromophenethylamine","AmineCount":1,"Formula":"Br","Name":"hydrobromide","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 118.848 78.276\"\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 0h119v79H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m19.213 1.038 9.914 5.724M32.411 12.579v11.319\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m32.411 23.898-13.208 7.62M32.411 26.713l-10.77 6.214\"/\u003e\u003c/g\u003e\u003cpath d=\"M19.203 31.518v15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m19.203 46.758 13.208 7.62M21.641 45.35l10.77 6.213\"/\u003e\u003c/g\u003e\u003cpath d=\"m32.411 54.378 13.208-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M45.619 46.758v-15.24M43.18 45.35V32.927\"/\u003e\u003c/g\u003e\u003cpath d=\"m32.411 23.898 13.208 7.62M45.619 31.518l13.197-7.622M58.816 23.896l13.199 7.618M72.015 31.514l10.044-5.801M32.411 54.378v11.319M35.686 71.509l9.923 5.729M19.203 46.758 7.771 53.361\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M34.67 8.655q0 .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-.881t1.274-.316q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.863 0q0 .923.386 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.392.524-.392 1.452\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M87.153 26.342h-.72l-2.62-4.066h-.029l.029.595q.024.357.024.732v2.739h-.565v-4.9h.714l2.607 4.054h.03l-.018-.327q-.012-.22-.023-.476-.006-.262-.006-.483v-2.768h.577zM91.459 26.342h-.619v-2.286h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.619zM93.964 27.831h-1.943v-.3l.771-.779q.222-.221.372-.393.154-.175.232-.339.079-.168.079-.364 0-.243-.147-.368-.143-.129-.371-.129-.215 0-.379.075-.161.075-.328.207l-.193-.242q.171-.147.393-.247.225-.1.507-.1.411 0 .65.207t.239.575q0 .229-.096.433-.093.2-.265.396-.167.196-.392.418l-.615.604v.017h1.486z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M34.67 69.615q0 .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-.881t1.274-.316q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.863 0q0 .923.386 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.392.524-.392 1.452\" class=\"atom\"/\u003e\u003cpath fill=\"#a62929\" stroke=\"none\" d=\"M1.959 51.353q.917 0 1.387.274.47.268.47.941 0 .434-.244.72-.238.286-.69.363v.036q.309.047.559.178t.393.375q.149.239.149.62 0 .666-.458 1.029-.459.364-1.245.364H.56v-4.9zm.119 2.09q.631 0 .863-.203.238-.202.238-.601 0-.405-.285-.577-.286-.179-.911-.179h-.81v1.56zm-.905.512v1.774h.988q.655 0 .905-.25.256-.256.256-.667 0-.381-.268-.619-.262-.238-.94-.238zm5.476-1.447q.101 0 .22.012.125.006.208.03l-.071.553q-.089-.018-.196-.029-.108-.018-.203-.018-.28 0-.53.154-.244.155-.393.435-.148.274-.148.649v1.959h-.602v-3.674h.494l.066.667h.03q.178-.297.458-.518.28-.22.667-.22\" class=\"atom\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M29.127 6.762 24.17 3.9M32.411 12.579v5.66\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m82.059 25.713-5.022 2.901\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M32.411 65.697v-5.659M35.686 71.509l4.962 2.865\" class=\"hi\"/\u003e\u003cpath stroke=\"#a62929\" d=\"m7.771 53.361 5.716-3.302\" class=\"hi\"/\u003e\u003c/g\u003e\u003cg class=\"mol\"\u003e\u003cg fill=\"#a62929\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M113.169 36.688q.917 0 1.387.274.471.268.471.941 0 .434-.244.72-.239.286-.691.363v.036q.31.048.56.179t.392.375q.149.238.149.619 0 .667-.458 1.03t-1.244.363h-1.721v-4.9zm.119 2.09q.631 0 .863-.202.239-.203.239-.602 0-.404-.286-.577-.286-.179-.911-.179h-.81v1.56zm-.905.512v1.774h.989q.654 0 .905-.25.255-.256.255-.667 0-.381-.267-.619-.262-.238-.941-.238zm5.476-1.447q.101 0 .22.012.125.006.209.03l-.072.554q-.089-.018-.196-.03-.107-.018-.203-.018-.279 0-.529.155-.245.155-.393.434-.149.274-.149.649v1.959h-.601v-3.673h.494l.065.667h.03q.179-.298.458-.518.28-.221.667-.221M111.209 41.588h-.62v-2.286h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.62z\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"2,5-Dimethoxy-4-bromophenethylamine hydrobromide","UNII":"GE2MXV3PWY"}],"Salts":["hydrochloride","hydrobromide"],"Scheduling":[{"gov":"Australia","ref":[],"schedule":"Schedule 9 substance"},{"gov":"Brazil","ref":[],"schedule":"F2 substance"},{"gov":"Canada","ref":[],"schedule":"Schedule III substance"},{"gov":"Germany","ref":[],"schedule":"Anlage I substance"},{"gov":"United Kingdom","ref":[],"schedule":"Class A substance"},{"act":"Controlled Substances Act (CSA)","gov":"United States","ref":[],"schedule":"Schedule I"},{"act":"Convention on Psychotropic Substances 1971","gov":"United Nations","ref":[],"schedule":"Schedule II drug"}],"Slang":["Eros ","Nexus ","Venus ","Spectrum ","Toonies "],"StereoisomerData":[],"Stereoisomers":[],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 94.524 78.276\"\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 0h95v79H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m19.213 1.038 9.914 5.724M32.411 12.579v11.319\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m32.411 23.898-13.208 7.62M32.411 26.713l-10.77 6.214\"/\u003e\u003c/g\u003e\u003cpath d=\"M19.203 31.518v15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m19.203 46.758 13.208 7.62M21.641 45.35l10.77 6.213\"/\u003e\u003c/g\u003e\u003cpath d=\"m32.411 54.378 13.208-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M45.619 46.758v-15.24M43.18 45.35V32.927\"/\u003e\u003c/g\u003e\u003cpath d=\"m32.411 23.898 13.208 7.62M45.619 31.518l13.197-7.622M58.816 23.896l13.199 7.618M72.015 31.514l10.044-5.801M32.411 54.378v11.319M35.686 71.509l9.923 5.729M19.203 46.758 7.771 53.361\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M34.67 8.655q0 .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-.881t1.274-.316q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.863 0q0 .923.386 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.392.524-.392 1.452\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M87.153 26.342h-.72l-2.62-4.066h-.029l.029.595q.024.357.024.732v2.739h-.565v-4.9h.714l2.607 4.054h.03l-.018-.327q-.012-.22-.023-.476-.006-.262-.006-.483v-2.768h.577zM91.459 26.342h-.619v-2.286h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.619zM93.964 27.831h-1.943v-.3l.771-.779q.222-.221.372-.393.154-.175.232-.339.079-.168.079-.364 0-.243-.147-.368-.143-.129-.371-.129-.215 0-.379.075-.161.075-.328.207l-.193-.242q.171-.147.393-.247.225-.1.507-.1.411 0 .65.207t.239.575q0 .229-.096.433-.093.2-.265.396-.167.196-.392.418l-.615.604v.017h1.486z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M34.67 69.615q0 .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-.881t1.274-.316q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.863 0q0 .923.386 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.392.524-.392 1.452\" class=\"atom\"/\u003e\u003cpath fill=\"#a62929\" stroke=\"none\" d=\"M1.959 51.353q.917 0 1.387.274.47.268.47.941 0 .434-.244.72-.238.286-.69.363v.036q.309.047.559.178t.393.375q.149.239.149.62 0 .666-.458 1.029-.459.364-1.245.364H.56v-4.9zm.119 2.09q.631 0 .863-.203.238-.202.238-.601 0-.405-.285-.577-.286-.179-.911-.179h-.81v1.56zm-.905.512v1.774h.988q.655 0 .905-.25.256-.256.256-.667 0-.381-.268-.619-.262-.238-.94-.238zm5.476-1.447q.101 0 .22.012.125.006.208.03l-.071.553q-.089-.018-.196-.029-.108-.018-.203-.018-.28 0-.53.154-.244.155-.393.435-.148.274-.148.649v1.959h-.602v-3.674h.494l.066.667h.03q.178-.297.458-.518.28-.22.667-.22\" class=\"atom\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M29.127 6.762 24.17 3.9M32.411 12.579v5.66\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m82.059 25.713-5.022 2.901\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M32.411 65.697v-5.659M35.686 71.509l4.962 2.865\" class=\"hi\"/\u003e\u003cpath stroke=\"#a62929\" d=\"m7.771 53.361 5.716-3.302\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Subjective Effects":null,"Title":"2,5-Dimethoxy-4-bromophenethylamine","UNII":"V77772N32H","Wikidata":"Q229942","Wikipedia":"2C-B","XLogP":2.1}