Cannabaceae

3-Fluoromethamphetamine
Ball-and-stick model of the 3-fluoromethamphetamine molecule
Legal status
Legal status
  • CA: Schedule I[1]
  • DE: Anlage I (Authorized scientific use only)
  • UK: Class A
  • US: Unscheduled
Identifiers
  • (RS)-1-(3-fluorophenyl)-N-methylpropan-2-amine
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC10H14FN
Molar mass167.227 g·mol−1
3D model (JSmol)
  • FC1=CC=CC(CC(NC)C)=C1
  • InChI=1S/C10H14FN/c1-8(12-2)6-9-4-3-5-10(11)7-9/h3-5,7-8,12H,6H2,1-2H3
  • Key:RRVAUTPWWWFYQT-UHFFFAOYSA-N

3-Fluoromethamphetamine (3-FMA) is a stimulant drug related to methamphetamine and 3-fluoroamphetamine. It has been sold online as a designer drug.[2][3][4][5]

Legal Status[edit]

Canada[edit]

As of 1996, 3-FMA is a controlled substance in Canada, due to being an analog of methamphetamine.[1]

China[edit]

As of October 2015, 3-FMA is a controlled substance in China.[6]

United States[edit]

As a close analog of scheduled controlled substance,[7] sale or possession of 3-FMA could be potentially be prosecuted under the Federal Analogue Act.[8]

See also[edit]

References[edit]

  1. ^ a b Branch, Legislative Services (2022-03-31). "Consolidated federal laws of Canada, Controlled Drugs and Substances Act". laws-lois.justice.gc.ca. Archived from the original on 2022-06-11. Retrieved 2022-08-11.
  2. ^ Westphal F, Rösner P, Junge T (January 2010). "Differentiation of regioisomeric ring-substituted fluorophenethylamines with product ion spectrometry". Forensic Science International. 194 (1–3): 53–9. doi:10.1016/j.forsciint.2009.10.007. PMID 19900772.
  3. ^ Nakanishi K, Miki A, Zaitsu K, Kamata H, Shima N, Kamata T, et al. (April 2012). "Cross-reactivities of various phenethylamine-type designer drugs to immunoassays for amphetamines, with special attention to the evaluation of the one-step urine drug test Instant-View, and the Emit assays for use in drug enforcement". Forensic Science International. 217 (1–3): 174–81. doi:10.1016/j.forsciint.2011.11.003. PMID 22154438.
  4. ^ Kauppila TJ, Flink A, Haapala M, Laakkonen UM, Aalberg L, Ketola RA, Kostiainen R (July 2011). "Desorption atmospheric pressure photoionization-mass spectrometry in routine analysis of confiscated drugs". Forensic Science International. 210 (1–3): 206–12. doi:10.1016/j.forsciint.2011.03.018. PMID 21474259.
  5. ^ Nakazono Y, Tsujikawa K, Kuwayama K, Kanamori T, Iwata YT, Miyamoto K, Kasuya F, Inoue H (July 2013). "Differentiation of regioisomeric fluoroamphetamine analogs by gas chromatography–mass spectrometry and liquid chromatography–tandem mass spectrometry". Forensic Toxicology. 31 (2): 241–250. doi:10.1007/s11419-013-0184-7. S2CID 23323323.
  6. ^ "关于印发《非药用类麻醉药品和精神药品列管办法》的通知" (in Chinese). China Food and Drug Administration. 27 September 2015. Archived from the original on 1 October 2015. Retrieved 1 October 2015.
  7. ^ Rösner P, Quednow B, Girreser U, Junge T (March 2005). "Isomeric fluoro-methoxy-phenylalkylamines: a new series of controlled-substance analogues (designer drugs)". Forensic Science International. 148 (2–3): 143–56. doi:10.1016/j.forsciint.2004.05.003. PMID 15639609.
  8. ^ "Federal Controlled Substance Analogue Act Summary". Erowid Analog Law Vault.

One thought on “Cannabaceae

  1. Well, that’s interesting to know that Psilotum nudum are known as whisk ferns. Psilotum nudum is the commoner species of the two. While the P. flaccidum is a rare species and is found in the tropical islands. Both the species are usually epiphytic in habit and grow upon tree ferns. These species may also be terrestrial and grow in humus or in the crevices of the rocks.
    View the detailed Guide of Psilotum nudum: Detailed Study Of Psilotum Nudum (Whisk Fern), Classification, Anatomy, Reproduction

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