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3-MMC

3-MMC molecule structure3-MMC molecule structure
3-Methylmethcathinone
Metaphedrone, 3M, meow, mcat, 3-meph
Psychoactive Class
Chemical Class

3-MMC is a synthetic stimulant-entactogen of the substituted cathinone class.citation needed It is a structural isomer of mephedrone (4-MMC) and first appeared in Sweden in 2012 as a designer drug alternative following mephedrone's widespread prohibition. It quickly gained presence on the online research chemical market and has frequently been marketed as a mephedrone substitute. Insufflation of this substance is reported to be notably painful.

Dosage & Duration

Dosage

Doses are population estimates that vary widely between individuals.

Threshold~25 mg
Light25-75 mg
Moderate75-150 mg
Strong150-300 mg
Heavy300+ mg
Bioavailability
~7%

Duration

Onset10-30 minutes
Come Up30-60 minutes
Peak2-3 hours
Offset1-1.5 hours
After Effects2-4 hours
Total4-6 hours
Half-life
~50 minutes

Subjective Effects

Legacy content. A statistically backed ontology from Mindstate Design Labs is coming soon.

Effects vary widely by individual, dose, and context.

Forked from Subjective Effect Documentation work byJosie Kins August 2016.

Reagent Testing

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

Mandelin(MD)
yellow2 → orange2 → red2 → brown2 → yellow2
Liebermann(LB)
white → orange2 → yellow2
Morr(MO)
pink2 → purple2
Simons(SI)
orange1 → blue1 → blue1 → blue2
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Pharmacology

Pharmacodynamics

3-MMC acts as a monoamine transporter substrate that potently releases dopamine and norepinephrine and inhibits their reuptake at the respective transporters.citation needed It displays moderate serotonin releasing activity, with greater selectivity for dopamine and especially norepinephrine over serotonin as a releasing agent. 3-MMC binds to serotonin 5-HT1A, 5-HT2A, and 5-HT2C receptors and adrenergic α1A and α2A receptors, with substantially stronger affinity at the adrenergic sites. It lacks agonist activity at the 5-HT2A receptor and is inactive at rat and human TAAR1.

Pharmacokinetics

The oral bioavailability of 3-MMC has been estimated at approximately 7% in a pig study, with peak blood concentrations attained within 5 to 10 minutes and an elimination half-life of roughly 50 minutes.1 Plasma concentrations fell below the limit of detection 24 hours after oral ingestion.citation needed The metabolic pathway is not well characterized but is thought to involve β-keto-reduction followed by N-demethylation.

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.

5-HTPAlcoholDXMDissociativesMAOIsMDMAMXENBOMe compoundsSNRIsSSRIsSerotonin releasersStimulantsTramadol
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Tolerance

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

Full Tolerance
Repeated 3-MMC use over time can produce tolerance across many effects, leading users to need larger doses for similar results. The compound's strong compulsive-redosing potential can speed tolerance development during prolonged sessions.
Baseline Reset
1-2 weeks
Half Tolerance
3-7 days
Cross Tolerance

Dopaminergic stimulants

Harm Potential

Addiction & Dependence

Psychological

High

3-MMC is described as extremely addictive with a high potential for abuse, reportedly more so than mephedrone.citation needed Its short-lived euphoric rush combined with dopaminergic effects produces intense compulsive redosing, with users commonly consuming 0.5-2 grams in multi-hour sessions despite intending smaller doses.

Physical

Moderate

Physical dependence can develop with chronic use. Cravings and withdrawal effects may occur upon sudden cessation, though specific withdrawal symptoms are not well-characterized in the literature.citation needed

Toxicity

Cardiovascular

Preliminary evidence suggests chronic high-dose use may carry cardiotoxic risks; acute effects include increased heart rate, elevated blood pressure, abnormal heartbeat, and vasoconstriction that can limit blood flow to organs.citation needed Heart valve issues have also been suggested but remain poorly characterized.

Central Nervous System

Preliminary evidence suggests chronic high-dose use may carry neurotoxic risks; symptoms of serotonin depletion are reported with overuse, manifesting as depression, cognitive fatigue, and motivation suppression during comedown periods.citation needed

Musculoskeletal

Rhabdomyolysis has been reported as a serious adverse effect,3 typically in cases involving hyperthermia and physical exertion.

Psychosis Risk

Delirium and confusion can occur at high doses, particularly when combined with temperature dysregulation, overheating, and inability to rest or rehydrate.citation needed Risk of delusions and mania may be elevated when combined with dissociatives.

Seizure Risk

Seizures are a rare but documented adverse effect,citation needed more likely in predisposed individuals or when taking heavy doses while dehydrated, undernourished, overheated, or fatigued.

History & Culture

Discovery and Emergence

3-MMC was first encountered in Sweden in 2012,citation needed emerging on the online research chemical market shortly after the banning of mephedrone in numerous countries. It was created as a designer drug specifically chosen to mimic and replace the functional and structural

Legality

International

UN Convention on Psychotropic Substances 1971 (Schedule II, placed March 2023)6

By Country

Illegal17
United States flagUnited StatesIllegal
Australia flagAustraliaIllegal
Austria flagAustriaIllegal
Belgium flagBelgiumIllegal
Brazil flagBrazilIllegal
China flagChinaIllegal
Czech Republic flagCzech RepublicIllegal
Denmark flagDenmarkIllegal
Germany flagGermanyIllegal
India flagIndiaIllegal
Netherlands flagNetherlandsIllegal
Norway flagNorwayIllegal
Poland flagPolandIllegal
South Africa flagSouth AfricaIllegal (analog/blanket ban)
Sweden flagSwedenIllegal
Turkey flagTurkeyIllegal
United Kingdom flagUnited KingdomIllegal
Controlled / restricted1
Switzerland flagSwitzerlandRestricted

References

Source Pages

  1. Drug Users Bible - 3-MMC
  2. Drug Users Bible by Dominic Milton Trott
  3. Erowid Experience Vaults: 3-MMC
  4. Isomer Design - 3-MMC
  5. Isomer Design (TiHKAL/PiHKAL)
  6. PsychonautWiki
  7. TripSit Factsheet: 3-MMC
  8. TripSit Factsheet: 3-MMC
  9. TripSit Factsheets
  10. Wikipedia

Citations

  1. Jakob A Shimshoni, Malka Britzi, Eyal Sobol, Udi Willenz, David Nutt, & Nir Edery. (June 2015). 3-Methyl-methcathinone: Pharmacokinetic profile evaluation in pigs in relation to pharmacodynamics. Journal of Psychopharmacology, 29(6), 734–43. https://doi.org/10.1177/02698811155766871
  2. Giampietro Frison, Samuela Frasson, Flavio Zancanaro, Gianpaola Tedeschi, & Luca Zamengo. (August 2016). Detection of 3-methylmethcathinone and its metabolites 3-methylephedrine and 3-methylnorephedrine in pubic hair samples by liquid chromatography-high resolution/high accuracy Orbitrap mass spectrometry. Forensic Science International, 265, 131–7. https://doi.org/10.1016/j.forsciint.2016.01.03912
  3. Critical review report: 3-Methylmethcathinone (3-MMC). (2022). https://cdn.who.int/media/docs/default-source/controlled-substances/45th-ecdd/3-mmc_draft.pdf1
  4. Clearmind Medicine Files Patent Application with USPTO for the Treatment of Dyskinesia. Clearmind Medicine Inc. (2023). https://www.clearmindmedicine.com/news-release/clearmind-medicine-files-patent-application-with-uspto-for-the-treatment-of-dyskinesia-further-strengthens-its-already-robust-ip-portfolio1
  5. Johannes G. Ramaekers, Johannes T. Reckweg, Natasha L. Mason, Kim P. C. Kuypers, Stefan W. Toennes, & Eef L. Theunissen. (December 2024). Safety and cognitive pharmacodynamics following dose escalations with 3-methylmethcathinone (3-MMC): a first in human, designer drug study. Neuropsychopharmacology, 50(7), 1084–1092. https://doi.org/10.1038/s41386-024-02042-71
  6. UNODC: CND decision on international control of ADB-BUTINACA, alpha-PiHP and 3-methylmethcathinone enters into force (November 2023). United Nations Office on Drugs and Crime (2023). https://www.unodc.org/LSS/Announcement/Details/1bed4cda-749e-4410-beb8-2b9cab02bcb21
  7. Customs (Prohibited Imports) Regulations 1956. legislation.gov.au (n.d.). https://www.legislation.gov.au/F1996B03651/2026-03-26/2026-03-26/text/original/epub/OEBPS/document_1/document_1.html1
  8. Suchtgiftverordnung, Annex V (RIS Bundesrecht konsolidiert). ris.bka.gv.at (n.d.). https://www.ris.bka.gv.at/Dokumente/Bundesnormen/NOR40250737/NOR40250737.pdf1
  9. Royal Decree of 6 September 2017 regulating narcotic and psychotropic substances, as amended by the Royal Decree 2023-02-08/06. ejustice.just.fgov.be (n.d.). https://www.ejustice.just.fgov.be/eli/arrete/2017/09/06/2017031231/justel1
  10. Royal Decree of 6 September 2017 regulating narcotic and psychotropic substances, as amended by the Royal Decree 2023-02-08/06. ejustice.just.fgov.be (n.d.). https://www.ejustice.just.fgov.be/cgi_loi/article.pl?language=fr&lg_txt=f&cn_search=20230208061

Further Reading

  1. Adamowicz et al. 2016 - Blood Concentrations Study
  2. Aknouche et al. 2022 - Fatal Rectal Injection Case
  3. EMCDDA: Initial Report 2022
  4. Jellinek - 3-MMC Information
  5. Luethi et al. 2018 - Monoamine Transporter Study
  6. Margasinska-Olejak et al. 2024 - Pharmacological Profile Review
  7. Shimshoni et al. - Pharmacokinetic Profile Study

Article Status

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    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

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

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