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CSA Names: 3-FMC
CSA Location: Schedule I Section (d) Subsection (65) DEA code 1233
Schedule I Section (h) Subsection (18) DEA code 1233
CSA History: 79 FR 4429 proposed to add (for two years) via the emergency scheduling provision of 21 USC 811(h) on 28 Jan 2014
81 FR 11479 proposed to add on 4 Mar 2016
79 FR 12938 added (for two years) via the emergency scheduling provision of 21 USC 811(h) effective 7 Mar 2014
80 FR 14842 renumbered effective 20 Mar 2015
Names: 1-(3-Fluorophenyl)-2-(methylamino)propan-1-one (IUPAC)
Molecular formula: C10H12FNO
Nominal mass: 181
Average mass: 181.2068
Monoisotopic mass: 181.090292
CAS registry number: 1049677-77-1
ChemSpider: 24958236
PubChem: 53415330
Wikipedia: 3-Fluoromethcathinone
Drugs-Forum: 3-FMC
Standard InChI: InChI=1S/C10H12FNO/c1-7(12-2)10(13)8-4-3-5-9(11)6-8/h3-7,12H,1-2H3
SMILES: CNC(C(=O)c1cccc(c1)F)C
Tags: cathinone,USCSA
Property Value Remarks
Property Value Remarks
Location Type Remarks
3-FMC GCMS Cayman.pdf MS Cayman Spectral Library
3-Fluoromethcathinone edit.pdf SP-GC-IR DiscovIR
Vendor ID URL
Cayman Chemical 10730
Cerilliant F-016
Title Publication Date Vol. Iss. Page(s) Remarks
Consideration of the Cathinones 2010-03-00 Advisory Council on the Misuse of Drugs
Screening of seized emerging drugs by ultra-high performance liquid chromatography with photodiode array ultraviolet and mass spectrometric detection. DOI: 10.1016/j.forsciint.2014.01.018 For. Sci. Int. 2014-04-01 Vol 237 L. Li and I. S. Lurie
Analysis and characterization of the novel psychoactive drug Forensic Science International 2014-11-01 Vol 244 (e56-e59) Magdalena Taschwer et al
Forensic Analysis of Cathinones Forensic Science Review 2013-01-01 Vol 25 (48-64) L. Gautam, A. Shanmuganathan, M. D. Cole
Direct analysis in real time mass spectrometry (DART-MS) of “bath salt” cathinone drug mixtures Analyst 2013-01-01 Vol 138 (3424-3432) Ashton D. Lesiak et al
Cathinone derivatives: A review of their chemistry, pharmacology and toxicology Drug Testing and Analysis 2011-01-01 Vol 3 (439-453) John P. Kelly et al
Ring positional differentiation of isomeric N-alkylated fluorocathinones by gas chromatography/tandem mass spectrometry. DOI: 10.1016/j.forsciint.2012.08.011 For. Sci. Int. 2012-11-01 Vol 223 Folker Westphal and Thomas Junge
Database ID URL
SWGDRUG Monographs 3-FMC Monograph
SWGDRUG Mass Spectral Library
Substance name
Substance name
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