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3-FPM

3-FPM molecule structure3-FPM molecule structure
3-Fluorophenmetrazine
PAL-593, 3-FPH, 3F-Phenmetrazine
Psychoactive Class

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.

Threshold5 mg
Light10-20 mg
Moderate20-35 mg
Strong35-50 mg
Heavy50+ mg

Duration

Onset5 minutes
Total3-6 hours

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.

Increased perspirationVasoconstriction

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.

Forked from Subjective Effect Documentation byJosie Kins September 2015.

Reagent Testing

Expected colorimetric results for common reagent tests. Colors show reaction change over 1–2 minutes.

Mandelin(MD)
yellow2 → orange2 → red2
Liebermann(LB)
white → yellow2 → orange2
Gallic(GA)
pink1
Morr(MO)
pink2 → green1
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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.

Interactions

Dangerous

Highest risk

These combinations are considered extremely harmful and should always be avoided. Reactions to these drugs taken in combination are highly unpredictable and have a potential to cause death.

AlcoholDXMDissociativesMAOIsMDMAMXENBOMe compoundsStimulantsTramadol
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Tolerance

Tolerance timelines are rules of thumb, not exact schedules, and vary widely between individuals and use patterns.

Full Tolerance
Tolerance to many effects develops with prolonged, repeated use, requiring increasingly large doses to achieve comparable effects.
Baseline Reset
Tolerance returns to baseline after approximately 1-2 weeks without further use.
Half Tolerance
Tolerance is reduced by approximately half after 3-7 days without further use.
Cross Tolerance

Dopaminergic stimulants

Harm Potential

Addiction & Dependence

Psychological

Moderate

Chronic 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

Lethal Dosage

The exact toxic dose is unknown.

Systemic inflammatory response

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

Illegal14
United States flagUnited StatesIllegal (analog/blanket ban)
Argentina flagArgentinaIllegal
Australia flagAustraliaIllegal (analog/blanket ban)
Austria flagAustriaIllegal (analog/blanket ban)
Brazil flagBrazilIllegal
Czech Republic flagCzech RepublicIllegal
Germany flagGermanyIllegal (analog/blanket ban)
Israel flagIsraelIllegal
Netherlands flagNetherlandsIllegal (analog/blanket ban)
Poland flagPolandIllegal
Singapore flagSingaporeIllegal
Sweden flagSwedenIllegal
Switzerland flagSwitzerlandIllegal
Ukraine flagUkraineIllegal
Controlled / restricted2
Ireland flagIrelandRestricted
United Kingdom flagUnited KingdomRestricted
Not scheduled3
France flagFranceNot scheduled
India flagIndiaNot scheduled
Spain flagSpainNot scheduled

References

Source Pages

  1. Drug Users Bible by Dominic Milton Trott
  2. Erowid Novel Drug Briefs: 3-FPM
  3. Erowid: 3-FPM Vault
  4. Erowid: 3F-Phenmetrazine Vault
  5. Isomer Design (TiHKAL/PiHKAL)
  6. PsychonautWiki
  7. The Drug Classroom
  8. TripSit Factsheet: 3-FPM
  9. TripSit Factsheets
  10. Wikipedia
  11. Wikipedia: 3 Fluorophenmetrazine

Citations

  1. Decreto N° 560/2019. argentina.gob.ar (n.d.). https://www.argentina.gob.ar/normativa/nacional/decreto-560-2019-326675/actualizacion1
  2. Decreto N° 560/2019. argentina.gob.ar (n.d.). https://www.argentina.gob.ar/normativa/326675_dec560-1_pdf/archivo1
  3. Decreto N° 560/2019. argentina.gob.ar (n.d.). https://www.argentina.gob.ar/normativa/nacional/ley-23737-138/actualizacion1
  4. 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
  5. 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
  6. 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
  7. 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
  8. 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
  9. 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
  10. 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

  1. Backberg et al. 2016 - Adverse events related to 3-FPM (STRIDA project)
  2. Blough et al. 2011 - Phenylmorpholines patent
  3. Gibbons et al. 2016 - Emerging NPS in the United Kingdom
  4. Mayer et al. 2017 - Acute kidney injury and limb ischaemia with 3-FPM
  5. Pifl et al. 2017 - Fluorinated phenmetrazine as monoamine transporter substrates
  6. Soh & Elliott 2014 - Phenmetrazine pharmacology review
  7. Welter et al. 2017 - 3-FPM metabolism and biotransformation

Article Status

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    An autonomous workflow built by Josie Kins compiled this article's foundation from information published across the web.

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Recent changes7 human edits · latest

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24 January 2026

  1. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  2. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  3. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  4. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  5. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  6. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  7. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

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