{"Abbreviation":["2C-H"],"Aliases":["NSC 168525","Dtxcid40112055","625-021-8","2-(2,5-Dimethoxyphenyl)ethanamine","2-(2,5-Dimethoxy-phenyl)-ethylamine","2-(2,5-Dimethoxyphenyl)Ethan-1-Amine","2C-H","2,5-Dimethoxyphenethylamine-d6","2-(2,5-Dimethoxyphenyl)Ethylamine","Chembl287047","NSC-168525","benzeneethanamine, 2,5-dimethoxy-","Schembl479514","Schembl7558636","DEA No. 7517","Schembl29491077","(2,5-Dimethoxyphenyl)ethylamine","Chebi:125507","BNB44277","Bdbm50026778","NSC168525","2-(2,5-Dimethoxyphenyl)ethanamine #","Akos000162038","AC-6627","Phenethylamine, 2,5-dimethoxy-","DB-027456","NS00015658","2-(2-Aminoethyl)-1,4-dimethoxybenzene","Brd-k20985754-001-01-9"],"CAS":"3600-86-0","ChemicalClasses":["2,5-dimethoxyphenethylamine"],"Chirality":"achiral","DTXSID":"80189564","EliminationHalfLife":"","Erowid Experience Reports":[{"Author":"PandaDoom","Id":80334,"Title":"So Happy, Very Happy"}],"Esters":[],"European Community (EC) Number":"625-021-8","Formating":[],"HeavyAtomCount":13,"IUPACName":"2-(2,5-dimethoxyphenyl)ethanamine","InChI":"InChI=1S/C10H15NO2/c1-12-9-3-4-10(13-2)8(7-9)5-6-11/h3-4,7H,5-6,11H2,1-2H3","InChIKey":"WNCUVUUEJZEATP-UHFFFAOYSA-N","MeSH Headers":[],"MolecularFormula":"C\u003csub\u003e10\u003c/sub\u003eH\u003csub\u003e15\u003c/sub\u003eNO\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"181.23 g/mol","PD":"PD046579","PubChemId":76632,"PubChemTitle":"2,5-Dimethoxyphenethylamine","Reagents":[{"Colors":["#ffffff","#f0d41d","#7aefa6","#3f8a1f"],"Name":"Marquis"},{"Colors":["#ffffff","#f0d41d","#3f8a1f"],"Name":"Mecke"},{"Colors":["#f0d41d","#fd7322","#51240b"],"Name":"Mandelin"},{"Colors":["#ffffff","#3f8a1f"],"Name":"Froehde"},{"Colors":[],"Name":"Simon's"},{"Colors":[],"Name":"Scott"}],"Record Description":["2C (2C-x) is a general name for the family of psychedelic phenethylamines containing methoxy groups on the 2 and 5 positions of a benzene ring. Most of these compounds also carry lipophilic substituents at the 4 position, usually resulting in more potent and more metabolically stable and longer acting compounds. Most of the currently known 2C compounds were first synthesized by Alexander Shulgin in the 1970s and 1980s, and published in his book, PiHKAL (Phenethylamines i Have Known And Loved). Dr. Shulgin also invented the term 2C, being an acronym for the 2 carbon atoms between the benzene ring and the amino group.[1] Shulgin, Alexander; Ann Shulgin (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.","Wikipedia|PiHKAL|Phenethylamines"],"Records":{"UNII":{"Impurities":[]}},"Reddit Experience Reports":[],"RefChem":"82916","RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/2C-H","Name":"2,5-Dimethoxyphenethylamine","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q4633049","Name":"2,5-Dimethoxyphenethylamine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/76632","Name":"2,5-Dimethoxyphenethylamine","Sub":false}]},{"Name":"Probes \u0026 Drugs","Urls":[{"Link":"https://www.probes-drugs.org/compound/PD046579","Name":"2,5-Dimethoxyphenethylamine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=3600-86-0","Name":"2,5-Dimethoxyphenethylamine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/9A8XF4GA0X","Name":"2,5-Dimethoxyphenethylamine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID80189564","Name":"2,5-Dimethoxyphenethylamine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 76632, 2,5-Dimethoxyphenethylamine. Accessed June 7, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/76632\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/76632\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxyphenethylamine. UNII: 9A8XF4GA0X. Global Substance Registration System. Accessed June 7, 2026. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/9A8XF4GA0X\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/9A8XF4GA0X\u003c/a\u003e"],"SMILES":"COC1=CC(=C(C=C1)OC)CCN","SaltData":[{"AcidCount":1,"Amine":"2,5-Dimethoxyphenethylamine","AmineCount":2,"Formula":"OS(=O)(=O)O","Name":"hemisulfate","RName":"sulfate","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 132.293 82.657\"\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=\".8\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h133v83H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m28.871 78.665-9.59-5.537M15.673 66.852V55.805\" class=\"bond\"/\u003e\u003cg 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