{"Abbreviation":"DMPEA","Aliases":["Homoveratrylamine","Benzeneethanamine, 3,4-dimethoxy-","3,4-Dimethoxyphenylethylamine","2-(3,4-Dimethoxyphenyl)ethylamine","Dimethoxydopamine","Dimethylmescaline","Dopamine dimethyl ether","DIMPEA","O,O-Dimethyldopamine","3,4-Dimethoxybenzeneethanamine"],"Boiling Point":"163 - 165 °C","CAS":"120-20-7","ChEBI":"CHEBI:136995","ChEMBL":"CHEMBL26019","ChemicalClasses":["catecholamine"],"Chirality":"achiral","Classes":["Monoamine oxidase inhibitor"],"DrugClasses":[],"EINECS":"204-376-9","Erowid Experience Reports":[],"European Community (EC) Number":"204-376-9","FullSalts":["3,4-Dimethoxyphenethylamine hydrochloride","3,4-Dimethoxyphenethylamine hydrobromide"],"HMDB ID":"HMDB0041806","HeavyAtomCount":13,"IUPACName":"2-(3,4-dimethoxyphenyl)ethanamine","InChI":"InChI=1S/C10H15NO2/c1-12-9-4-3-8(5-6-11)7-10(9)13-2/h3-4,7H,5-6,11H2,1-2H3","InChIKey":"ANOUKFYBOAKOIR-UHFFFAOYSA-N","MolecularFormula":"C\u003csub\u003e10\u003c/sub\u003eH\u003csub\u003e15\u003c/sub\u003eNO\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"181.23 g/mol","Physical Description":"Colorless liquid with an amine-like odor; [Alfa Aesar MSDS]","PrevSalts":["hydrochloride","hydrobromide"],"PubChemId":8421,"Record Description":["3,4-dimethoxyphenylethylamine is an aromatic ether that is the derivative of 2-phenylethylamine with methoxy substituents at the 3- and 4-positions. It is an alkaloid isolated from the Cactaceae family. It has a role as a plant metabolite and an allergen. It is a phenylethylamine, an aromatic ether and an alkaloid. It derives from a hydride of a 2-phenylethylamine.","3,4-Dimethoxyphenethylamine has been reported in Pilosocereus leucocephalus, Vachellia rigidula, and Ototropis elegans with data available.","A derivative of phenethylamine containing two substituent methoxy groups in the phenyl ring.","3,4-dimethoxyphenylethylamine is an aromatic ether that is the derivative of 2-phenylethylamine with methoxy substituents at the 3- and 4-positions. It is an alkaloid isolated from the Cactaceae family. It has a role as a plant metabolite and an allergen. It is a phenylethylamine, an aromatic ether and an alkaloid. It derives from a hydride of a 2-phenylethylamine.","Wikipedia|PiHKAL|Phenethylamines"],"RefCount":3,"References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/3,4-Dimethoxyphenethylamine","Name":"3,4-Dimethoxyphenethylamine","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q4634069","Name":"3,4-Dimethoxyphenethylamine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/8421","Name":"3,4-Dimethoxyphenethylamine","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL26019","Name":"3,4-Dimethoxyphenethylamine","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:136995","Name":"3,4-Dimethoxyphenethylamine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=120-20-7","Name":"3,4-Dimethoxyphenethylamine","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0041806","Name":"3,4-Dimethoxyphenethylamine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/IQF9T435OP","Name":"3,4-Dimethoxyphenethylamine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID8059506","Name":"3,4-Dimethoxyphenethylamine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 8421, 3,4-Dimethoxyphenethylamine. Accessed June 26, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/8421\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/8421\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 3,4-Dimethoxyphenethylamine. UNII: IQF9T435OP. Global Substance Registration System. Accessed June 26, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/IQF9T435OP\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/IQF9T435OP\u003c/a\u003e"],"SMILES":"COC1=C(C=C(C=C1)CCN)OC","Salts":["hydrochloride","hydrobromide"],"SaltsAcidCount":[1,1],"SaltsAmineCount":[1,1],"SaltsUNII":["TTV20379WY","ZZB3NR8KVD"],"Solubility":"24.8 [ug/mL] (The mean of the results at pH 7.4)","StoreUNII":["IQF9T435OP"],"StructureBase64":"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Effects":null,"Title":"3,4-Dimethoxyphenethylamine","UNII":"IQF9T435OP","Wikidata":"Q4634069","Wikipedia":"3,4-Dimethoxyphenethylamine","XLogP":0.8}