Citation noticeOur citation system is being overhauled
References and citation markers may currently be incomplete, mismatched, or incorrect. This system is being rebuilt and reviewed before the full site launch.
3-FPM
3-Fluorophenmetrazine is a synthetic phenylmorpholine stimulant and fluorinated derivative of phenmetrazine, a former anorectic. Its synthesis and pharmacology were first reported in a 2011 patent, with human use emerging through the online research chemical market in the mid-2010s. It is generally described as producing comparatively moderate, controlled stimulation with enhanced focus and motivation, although anecdotal reports indicate that serious nervous system reactions can occur in some individuals.
Dosage & Duration
Dosage
Doses are population estimates that vary widely between individuals.
Duration
Subjective Effects
Legacy content. A statistically backed ontology from Mindstate Design Labs is coming soon.
Effects vary widely by individual, dose, and context.
Physical
The physical effects of 3-FPM can be broken down into several components which progressively intensify proportional to dosage.
Cognitive
The cognitive effects of 3-FPM can be broken down into several components which progressively intensify proportional to dosage. It contains a large number of typical stimulant cognitive effects. Although negative side effects are usually mild at low to moderate doses, they become increasingly likely to manifest themselves with higher amounts or extended usage. This particularly holds true during the offset of the experience.
Pharmacology
Pharmacodynamics
3-FPM primarily acts as a norepinephrine-dopamine releasing agent by reversing monoamine transporters, increasing extracellular norepinephrine and dopamine. It releases serotonin with substantially lower potency. 3-FPM also inhibits dopamine and norepinephrine transporter-mediated uptake, while its effect on serotonin uptake is considerably weaker.
Pharmacokinetics
3-FPM undergoes N-oxidation, aryl hydroxylation followed by O-methylation, alkyl hydroxylation, oxidation, and degradation of the ethyl bridge. These pathways can produce an O/N-bis-dealkylated metabolite and combined transformation products, with further glucuronidation or sulfation.
Tolerance
Tolerance timelines are rules of thumb, not exact schedules, and vary widely between individuals and use patterns.
Dopaminergic stimulants
Harm Potential
Addiction & Dependence
Psychological
ModerateChronic use is considered moderately addictive, with high abuse potential and the capacity to produce psychological dependence in some users. Repeated dosing may become difficult to control, and established addiction may involve cravings after cessation.
Physical
Withdrawal effects may occur when use is stopped suddenly after addiction has developed.
Toxicity
The exact toxic dose is unknown.
Serious flu-like symptoms have occurred during the comedown, including muscle and joint aches, fever, chills, headaches, and occasional migraine auras.
History & Culture
3-FPM is a fluorinated analogue of phenmetrazine, an appetite suppressant that was clinically used in Europe during the 1950s and marketed through the 1960s and 1970s before being withdrawn amid concerns about abuse and addiction. Phenmetrazine was also alleged to have been used by The Beatles in…
Legality
International
3-FPM is not named in the INCB lists of narcotic drugs under the 1961 Convention or psychotropic substances under the 1971 Convention. It is also not named in the precursor tables of the 1988 Convention.
By Country
References
Source Pages
Citations
- Decreto N° 560/2019. argentina.gob.ar (n.d.). https://www.argentina.gob.ar/normativa/nacional/decreto-560-2019-326675/actualizacion1
- Decreto N° 560/2019. argentina.gob.ar (n.d.). https://www.argentina.gob.ar/normativa/326675_dec560-1_pdf/archivo1
- Decreto N° 560/2019. argentina.gob.ar (n.d.). https://www.argentina.gob.ar/normativa/nacional/ley-23737-138/actualizacion1
- Criminal Code Act 1995 and Criminal Code Regulations 2019. legislation.gov.au (n.d.). https://www.legislation.gov.au/C2004A04868/2025-01-09/2025-01-09/text/original/epub/OEBPS/document_2/document_2.html1
- Criminal Code Act 1995 and Criminal Code Regulations 2019. legislation.gov.au (n.d.). https://www.legislation.gov.au/F2019L00561/2025-03-01/2025-03-01/text/original/epub/OEBPS/document_1/document_1.html1
- Neue-Psychoaktive-Substanzen-Verordnung (NPSV) § 1 Abs. 1 Z 2, § 1 Abs. 2, Anlage II Nr. 2 (Phenethylamin-Verbindungen), issued under § 3 Neue-Psychoaktive-Substanzen-Gesetz (NPSG). ris.bka.gv.at (n.d.). https://www.ris.bka.gv.at/GeltendeFassung.wxe?Abfrage=Bundesnormen&Gesetzesnummer=200076421
- Neue-Psychoaktive-Substanzen-Verordnung (NPSV) § 1 Abs. 1 Z 2, § 1 Abs. 2, Anlage II Nr. 2 (Phenethylamin-Verbindungen), issued under § 3 Neue-Psychoaktive-Substanzen-Gesetz (NPSG). ris.bka.gv.at (n.d.). https://www.ris.bka.gv.at/Dokumente/Bundesnormen/NOR40261441/II_106_2024_Anlage_II.pdf1
- Neue-Psychoaktive-Substanzen-Verordnung (NPSV) § 1 Abs. 1 Z 2, § 1 Abs. 2, Anlage II Nr. 2 (Phenethylamin-Verbindungen), issued under § 3 Neue-Psychoaktive-Substanzen-Gesetz (NPSG). ris.bka.gv.at (n.d.). https://www.ris.bka.gv.at/eli/bgbl/II/2024/1061
- Neue-Psychoaktive-Substanzen-Verordnung (NPSV) § 1 Abs. 1 Z 2, § 1 Abs. 2, Anlage II Nr. 2 (Phenethylamin-Verbindungen), issued under § 3 Neue-Psychoaktive-Substanzen-Gesetz (NPSG). ris.bka.gv.at (n.d.). https://www.ris.bka.gv.at/Dokumente/Bundesnormen/NOR40134446/NOR40134446.html1
- SVS/MS Ordinance (Portaria) No. 344 of 12 May 1998, Annex I, as updated and republished by ANVISA RDC No. 1,036 of 9 July 2026 (DOU 13 July 2026). anvisalegis.datalegis.net (n.d.). https://anvisalegis.datalegis.net/action/ActionDatalegis.php?acao=abrirTextoAto&tipo=RDC&numeroAto=00001036&seqAto=000&valorAno=2026&orgao=RDC/DC/ANVISA/MS&codTipo=&desItem=&desItemFim=&cod_menu=1696&cod_modulo=134&pesquisa=true1
Further Reading
Backberg et al. 2016 - Adverse events related to 3-FPM (STRIDA project)
Blough et al. 2011 - Phenylmorpholines patent
Gibbons et al. 2016 - Emerging NPS in the United Kingdom
Mayer et al. 2017 - Acute kidney injury and limb ischaemia with 3-FPM
Pifl et al. 2017 - Fluorinated phenmetrazine as monoamine transporter substrates
Soh & Elliott 2014 - Phenmetrazine pharmacology review
Welter et al. 2017 - 3-FPM metabolism and biotransformation
Article Status
Step 1 · Automated synthesisAn autonomous workflow built by Josie Kins compiled this article's foundation from information published across the web.
- Step 2 · First-pass reviewPending
Not yet reviewed — this article is pending editorial review by Lyrea.
- Step 3 · Citation reviewPending
No one has reviewed this article's citations yet. That second pass checks each claim against the source it cites.
Recent changes7 human edits · latest
Times are UTCNewest first
24 January 2026
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
Suggest an edit
Spotted a mistake, an outdated claim, or something missing from the 3-FPM article? Send the editors a private note. Feedback lands in a moderation queue and is never shown on the site.
Wish to give generalised feedback? You can do so here.