{"Abbreviation":"","Aliases":["2-Aminoacetophenone","2-Amino-1-phenylethanone","2-Amino-1-phenylethan-1-one","2-Aminoecetophenone","Ethanone, 2-amino-1-phenyl-","2-amino-1-phenyl-ethanone","α-Aminoactophenone","α-Aminoacetophenone","α-Demethylcathinone","omega-Aminoacetophenone"],"CAS":"613-89-8","ChEBI":"CHEBI:104022","ChEMBL":"CHEMBL128079","ChemicalClasses":["phenethylamine"],"Chirality":"achiral","Classes":["Stimulant"],"DrugClasses":[],"DurationOfAction":"","EINECS":"210-358-1","EliminationHalfLife":"","European Community (EC) Number":"210-358-1","HMDB ID":"HMDB0032628","HeavyAtomCount":10,"IUPACName":"2-amino-1-phenylethanone","InChI":"InChI=1S/C8H9NO/c9-6-8(10)7-4-2-1-3-5-7/h1-5H,6,9H2","InChIKey":"HEQOJEGTZCTHCF-UHFFFAOYSA-N","Melting Point":"20 °C","MolecularFormula":"C\u003csub\u003e8\u003c/sub\u003eH\u003csub\u003e9\u003c/sub\u003eNO","MolecularWeight":"135.16 g/mol","Physical Description":"Liquid","PrevSalts":[],"PubChemId":11952,"Record Description":["2-amino-1-phenylethanone is an aromatic ketone.","2-Aminoacetophenone has been reported in Streptomyces and Zea mays with data available.","See also: Ethanone, 2-amino-1-phenyl-, hydrochloride (1:1) (annotation moved to); o-Aminoacetophenone (annotation moved to).","2-amino-1-phenylethanone is an aromatic ketone."],"RefCount":3,"References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/2-Aminoacetophenone","Name":"Phenacylamine","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q27181279","Name":"Phenacylamine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/11952","Name":"Phenacylamine","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL128079","Name":"Phenacylamine","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:104022","Name":"Phenacylamine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=613-89-8","Name":"Phenacylamine","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0032628","Name":"Phenacylamine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/4M571C83H7","Name":"Phenacylamine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID80210206","Name":"Phenacylamine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 11952, Phenacylamine. Accessed June 25, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/11952\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/11952\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Phenacylamine. UNII: 4M571C83H7. Global Substance Registration System. Accessed June 25, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/4M571C83H7\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/4M571C83H7\u003c/a\u003e"],"SMILES":"C1=CC=C(C=C1)C(=O)CN","Scheduling":[],"StoreUNII":["4M571C83H7"],"StructureBase64":"PHN2ZyB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciIHhtbG5zOnhsaW5rPSJodHRwOi8vd3d3LnczLm9yZy8xOTk5L3hsaW5rIiBoZWlnaHQ9IjQ5Ljg0OG1tIiB2ZXJzaW9uPSIxLjIiIHZpZXdCb3g9IjAgMCA3Ni4zNDYgNDkuODQ4IiB3aWR0aD0iNzYuMzQ2bW0iPgogICAgICAKICAgIDxkZXNjPkdlbmVyYXRlZCBieSB0aGUgQ2hlbWlzdHJ5IERldmVsb3BtZW50IEtpdCAoaHR0cDovL2dpdGh1Yi5jb20vY2RrKTwvZGVzYz4KICAgICAgCiAgICA8ZyBmaWxsPSIjMzA1MEY4IiBzdHJva2U9IiMwMDAwMDAiIHN0cm9rZS1saW5lY2FwPSJyb3VuZCIgc3Ryb2tlLWxpbmVqb2luPSJyb3VuZCIgc3Ryb2tlLXdpZHRoPSIuNyI+CiAgICAgICAgICAgIAogICAgICAgIDxyZWN0IGZpbGw9IiNGRkZGRkYiIGhlaWdodD0iNTAuMCIgc3Ryb2tlPSJub25lIiB3aWR0aD0iNzcuMCIgeD0iLjAiIHk9Ii4wIi8+CiAgICAgICAgICAgIAogICAgICAgIDxnIGNsYXNzPSJtb2wiIGlkPSJtb2wxIj4KICAgICAgICAgICAgICAgICAgCiAgICAgICAgICAgIDxnIGNsYXNzPSJib25kIiBpZD0ibW9sMWJuZDEiPgogICAgICAgICAgICAgICAgICAgICAgICAKICAgICAgICAgICAgICAgIDxsaW5lIHgxPSIxLjAzOCIgeDI9IjEuMDQzIiB5MT0iMjUuOTMzIiB5Mj0iNDEuMTgxIi8+CiAgICAgICAgICAgICAgICAgICAgICAgIAogICAgICAgICAgICAgICAgPGxpbmUgeDE9IjMuNDc3IiB4Mj0iMy40ODEiIHkxPSIyNy4zNCIgeTI9IjM5Ljc3NCIvPgogICAgICAgICAgICAgICAgICAgICAgCiAgICAgICAgICAgIDwvZz4KICAgICAgICAgICAgICAgICAgCiAgICAgICAgICAgIDxsaW5lIGNsYXNzPSJib25kIiBpZD0ibW9sMWJuZDIiIHgxPSIxLjAzOCIgeDI9IjE0LjIzNiIgeTE9IjI1LjkzMyIgeTI9IjE4LjMxMyIvPgogICAgICAgICAgICAgICAgICAKICAgICAgICAgICAgPGcgY2xhc3M9ImJvbmQiIGlkPSJtb2wxYm5kMyI+CiAgICAgICAgICAgICAgICAgICAgICAgIAogICAgICAgICAgICAgICAgPGxpbmUgeDE9IjI3LjQ0IiB4Mj0iMTQuMjM2IiB5MT0iMjUuOTQxIiB5Mj0iMTguMzEzIi8+CiAgICAgICAgICAgICAgICAgICAgICAgIAogICAgICAgICAgICAgICAgPGxpbmUgeDE9IjI1LjAwMiIgeDI9IjE0LjIzNiIgeTE9IjI3LjM0OSIgeTI9IjIxLjEyOSIvPgogICAgICAgICAgICAgICAgICAgICAgCiAgICAgICAgICAgIDwvZz4KICAgICAgICAgICAgICAgICAgCiAgICAgICAgICAgIDxsaW5lIGNsYXNzPSJib25kIiBpZD0ibW9sMWJuZDQiIHgxPSIyNy40NCIgeDI9IjI3LjQ0NCIgeTE9IjI1Ljk0MSIgeTI9IjQxLjE5Ii8+CiAgICAgICAgICAgICAgICAgIAogICAgICAgICAgICA8ZyBjbGFzcz0iYm9uZCIgaWQ9Im1vbDFibmQ1Ij4KICAgICAgICAgICAgICAgICAgICAgICAgCiAgICAgICAgICAgICAgICA8bGluZSB4MT0iMTQuMjQ2IiB4Mj0iMjcuNDQ0IiB5MT0iNDguODEiIHkyPSI0MS4xOSIvPgogICAgICAgICAgICAgICAgICAgICAgICAKICAgICAgICAgICAgICAgIDxsaW5lIHgxPSIxNC4yNDciIHgyPSIyNS4wMDYiIHkxPSI0NS45OTQiIHkyPSIzOS43ODIiLz4KICAgICAgICAgICAgICAgICAgICAgIAogICAgICAgICAgICA8L2c+CiAgICAgICAgICAgICAgICAgIAogICAgICAgICAgICA8bGluZSBjbGFzcz0iYm9uZCIgaWQ9Im1vbDFibmQ2IiB4MT0iMS4wNDMiIHgyPSIxNC4yNDYiIHkxPSI0MS4xODEiIHkyPSI0OC44MSIvPgogICAgICAgICAgICAgICAgICAKICAgICAgICAgICAgPGxpbmUgY2xhc3M9ImJvbmQiIGlkPSJtb2wxYm5kNyIgeDE9IjI3LjQ0IiB4Mj0iNDAuNjM4IiB5MT0iMjUuOTQxIiB5Mj0iMTguMzIxIi8+CiAgICAgICAgICAgICAgICAgIAogICAgICAgICAgICA8ZyBjbGFzcz0iYm9uZCIgaWQ9Im1vbDFibmQ4Ij4KICAgICAgICAgICAgICAgICAgICAgICAgCiAgICAgICAgICAgICAgICA8bGluZSB4MT0iMzkuNDE5IiB4Mj0iMzkuNDE5IiB5MT0iMTkuMDI1IiB5Mj0iNy4wMDIiLz4KICAgICAgICAgICAgICAgICAgICAgICAgCiAgICAgICAgICAgICAgICA8bGluZSB4MT0iNDEuODU3IiB4Mj0iNDEuODU3IiB5MT0iMTkuMDI1IiB5Mj0iNy4wMDIiLz4KICAgICAgICAgICAgICAgICAgICAgIAogICAgICAgICAgICAgICAgPGxpbmUgY2xhc3M9ImhpIiBzdHJva2U9IiNGRjBEMEQiIHgxPSIzOS40MTkiIHgyPSIzOS40MTkiIHkxPSI3LjAwMTk5OTk5OTk5OTk5OSIgeTI9IjEzLjAxMzQ5OTk5OTk5OTk5OSIvPgogICAgICAgICAgICAgICAgPGxpbmUgY2xhc3M9ImhpIiBzdHJva2U9IiNGRjBEMEQiIHgxPSI0MS44NTciIHgyPSI0MS44NTciIHkxPSI3LjAwMTk5OTk5OTk5OTk5OSIgeTI9IjEzLjAxMzQ5OTk5OTk5OTk5OSIvPgogICAgICAgICAgICA8L2c+CiAgICAgICAgICAgICAgICAgIAogICAgICAgICAgICA8bGluZSBjbGFzcz0iYm9uZCIgaWQ9Im1vbDFibmQ5IiB4MT0iNDAuNjM4IiB4Mj0iNTMuODM2IiB5MT0iMTguMzIxIiB5Mj0iMjUuOTQxIi8+CiAgICAgICAgICAgICAgICAgIAogICAgICAgICAgICA8bGluZSBjbGFzcz0iYm9uZCIgaWQ9Im1vbDFibmQxMCIgeDE9IjUzLjgzNiIgeDI9IjYzLjg4MSIgeTE9IjI1Ljk0MSIgeTI9IjIwLjE0MiIvPgogICAgICAgICAgICAgICAgICAKICAgICAgICAgICAgPHBhdGggY2xhc3M9ImF0b20iIGQ9Ik00Mi44OTcgMy4wNzhxLS4wIC43NTYgLS4yNTYgMS4zMjhxLS4yNTYgLjU2NSAtLjc1NiAuODgxcS0uNSAuMzE1IC0xLjI0NCAuMzE1cS0uNzU2IC4wIC0xLjI2MiAtLjMxNXEtLjUwNiAtLjMxNiAtLjc1NiAtLjg4N3EtLjI0NCAtLjU3MiAtLjI0NCAtMS4zMzRxLS4wIC0uNzUgLjI0NCAtMS4zMDlxLjI1IC0uNTY2IC43NTYgLS44ODFxLjUwNiAtLjMxNiAxLjI3NCAtLjMxNnEuNzMyIC4wIDEuMjMyIC4zMTZxLjUgLjMwOSAuNzU2IC44NzVxLjI1NiAuNTY1IC4yNTYgMS4zMjd6TTM5LjAzMyAzLjA3OHEuMCAuOTIzIC4zODcgMS40NTlxLjM5MyAuNTMgMS4yMjEgLjUzcS44MzkgLS4wIDEuMjIgLS41M3EuMzg3IC0uNTM2IC4zODcgLTEuNDU5cS4wIC0uOTI5IC0uMzg3IC0xLjQ1MnEtLjM4MSAtLjUyNCAtMS4yMDggLS41MjRxLS44MzQgLS4wIC0xLjIyNyAuNTI0cS0uMzkzIC41MjMgLS4zOTMgMS40NTJ6IiBmaWxsPSIjRkYwRDBEIiBpZD0ibW9sMWF0bTgiIHN0cm9rZT0ibm9uZSIvPgogICAgICAgICAgICAgICAgICAKICAgICAgICAgICAgPGcgY2xhc3M9ImF0b20iIGlkPSJtb2wxYXRtMTAiPgogICAgICAgICAgICAgICAgICAgICAgICAKICAgICAgICAgICAgICAgIDxwYXRoIGQ9Ik02OC45NzUgMjAuNzcxaC0uNzJsLTIuNjIgLTQuMDY2aC0uMDNxLjAxMiAuMjM4IC4wMyAuNTk1cS4wMjQgLjM1NyAuMDI0IC43MzJ2Mi43MzloLS41NjZ2LTQuOWguNzE1bDIuNjA3IDQuMDU1aC4wM3EtLjAwNiAtLjEwOCAtLjAxOCAtLjMyOHEtLjAxMiAtLjIyIC0uMDI0IC0uNDc2cS0uMDA2IC0uMjYyIC0uMDA2IC0uNDgydi0yLjc2OWguNTc4djQuOXoiIHN0cm9rZT0ibm9uZSIvPgogICAgICAgICAgICAgICAgICAgICAgICAKICAgICAgICAgICAgICAgIDxwYXRoIGQ9Ik03My4yODEgMjAuNzcx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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"],"Sensory Effects":[]},"Title":"Phenacylamine","UNII":"4M571C83H7","Wikidata":"Q27181279","Wikipedia":"2-Aminoacetophenone","XLogP":0.8}