2-Fluoromethamphetamine

Today we will delve into 2-Fluoromethamphetamine, a topic that has captured the attention of many in recent times. 2-Fluoromethamphetamine is something that has generated great interest in different areas, from science to pop culture. Over the years, 2-Fluoromethamphetamine has been the subject of study, debate and reflection, and its relevance is still present today. In this article we will explore different aspects related to 2-Fluoromethamphetamine, from its origins to its impact on modern society. We’ll dive into the history and meaning of 2-Fluoromethamphetamine, as well as its implications in various contexts. Prepare to enter a fascinating and intriguing universe, full of knowledge and discoveries about 2-Fluoromethamphetamine.

Stimulant designer drug

Not to be confused with 2-Fluoroamphetamine.

2-Fluoromethamphetamine (2-FMA) is a stimulant drug of the amphetamine family which has been used as a designer drug.[1][2][3] 2-FMA is commonly compared to lisdexamfetamine (Vyvanse), and dextroamphetamine due to its efficacy as a study or productivity aid.[citation needed] 2-FMA is purported to produce somewhat less euphoria than comparable amphetamines, likely due to its main mechanism of action consisting of norepinephrine reuptake inhibition.[4]

2-Fluoromethamphetamine
Ball-and-stick model of the 2-fluoromethamphetamine molecule
Clinical data
Routes of
administration		 By mouth
Legal status
Legal status
  • CA: Schedule I[5]
  • DE: Anlage I (Authorized scientific use only)
  • UK: Class A
  • US: Unscheduled
Identifiers
  • (RS)-1-(2-Fluorophenyl)-N-methylpropan-2-amine
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
Formula C10H14FN
Molar mass 167.227 g·mol−1
3D model (JSmol)
  • CC(CC1=CC=CC=C1F)NC
  • InChI=1S/C10H14FN/c1-8(12-2)7-9-5-3-4-6-10(9)11/h3-6,8,12H,7H2,1-2H3 checkY
  • Key:XNWIKJYFOIDUGD-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Chemistry

2-Fluoromethamphetamine is fluorinated analogue of methamphetamine, and is a regioisomer of 3-FMA and 4-FMA.

It does not activate the serotonin receptors, including 5-HT2A,[4] unlike most stimulant drugs of the amphetamine family.

Canada

As of 1996, 2-FMA is a controlled substance in Canada, due to being an analog of methamphetamine.[5]

China

As of October 2015, 2-FMA is a controlled substance in China.[6]

Germany

As of 13 December 2014, 2-FMA is a controlled substance in Germany.[7] It is controlled under Anlage I BtMG (Narcotics Act, Schedule I).[8] Substances controlled under Anlage I BtMG are illegal to manufacture, possess, import, export, buy, sell, procure or dispense it without a license. Violations of the law are punishable by a fine or imprisonment for up to five years.[9]

Ukraine

As of July 2019, 2-FMA is a controlled substance in Ukraine (considered a narcotic).[10]

United States

As a close analog of scheduled controlled substance,[1] sale or possession of 2-FMA could be potentially be prosecuted under the Federal Analogue Act.[11]

See also

References

  1. ^ a b 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): 143–156. doi:10.1016/j.forsciint.2004.05.003. PMID 15639609.
  2. ^ Camilleri A, Johnston MR, Brennan M, Davis S, Caldicott DG (April 2010). «Chemical analysis of four capsules containing the controlled substance analogues 4-methylmethcathinone, 2-fluoromethamphetamine, alpha-phthalimidopropiophenone and N-ethylcathinone». Forensic Science International. 197 (1–3): 59–66. doi:10.1016/j.forsciint.2009.12.048. PMID 20074881.
  3. ^ Ishii A, Sato K, Kusakabe K, Kato N, Wada T (February 2023). «Identification and Quantitative Analysis of 2-Fluoromethamphetamine and Its Metabolites in Human Urine». Journal of Analytical Toxicology. 47 (1): 59–65. doi:10.1093/jat/bkac026. PMID 35562170.
  4. ^ a b Åstrand A, Guerrieri D, Vikingsson S, Kronstrand R, Green H (December 2020). «In vitro characterization of new psychoactive substances at the μ-opioid, CB1, 5HT1A, and 5-HT2A receptors-On-target receptor potency and efficacy, and off-target effects». Forensic Science International. 317: 110553. doi:10.1016/j.forsciint.2020.110553. PMID 33160102. S2CID 226279968.
  5. ^ a b Legislative Services Branch (31 March 2022). «Consolidated federal laws of Canada, Controlled Drugs and Substances Act». laws-lois.justice.gc.ca. Archived from the original on 11 June 2022. Retrieved 11 August 2022.
  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. ^ Bundesgesetzblatt. «Achtundzwanzigste Verordnung zur Änderung betäubungsmittelrechtlicher Vorschriften – Vom 5. Dezember 2014» (in German). Bundesanzeiger-Verlags-GmbH. Retrieved 6 April 2022.
  8. ^ Bundesministerium der Justiz. «Gesetz über den Verkehr mit Betäubungsmitteln (Betäubungsmittelgesetz – BtMG) Anlage I (zu § 1 Abs. 1) (nicht verkehrsfähige Betäubungsmittel)» (in German). Retrieved 6 April 2022.
  9. ^ Bundesministerium der Justiz. «Gesetz über den Verkehr mit Betäubungsmitteln (Betäubungsmittelgesetz – BtMG) § 29 Straftaten» (in German). Retrieved 6 April 2022.
  10. ^ «Про внесення змін до Закону України «Про обіг в Україні наркотичних засобів, психотропних речовин, їх аналогів і прекурсорів»« (in Ukrainian). Verkhovna Rada of Ukraine. 23 July 2019. Archived from the original on 5 September 2021. Retrieved 6 September 2021.
  11. ^ «Federal Controlled Substance Analogue Act Summary». Erowid Analog Law Vault.