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    2-MMC molecular structure

    2-MMC Stats & Data

    Ortho 2-methyl mc Orthophedrone Orthomephedrone 2mmc ortomephedrone 2-methylmethcathinone 2methylmethcathinone
    NPS DataHub
    MW213.71
    FormulaC11H16ClNO
    CAS1246815-51-9
    IUPAC(2RS)-2-(Methylamino)-1-(2-methylphenyl)propan-1-one
    SMILES[Cl-].CNC(C)C(=O)c1ccccc1C.[H+]
    InChIKeyBNZJHCPXDZXUMH-UHFFFAOYSA-N
    Phenethylamines; Cathinones; 2020/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2021/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2022/1. Von 2-Phenethylamin abgeleitete Verbindungen
    Chemical Class Cathinone
    Psychoactive Class Stimulant / Entactogen

    Receptor Profile

    Receptor Actions

    Inhibitors
    Dopamine-norepinephrine reuptake inhibitor (higher affinity for DAT and NET than SERT)
    Other
    Serotonin-norepinephrine-dopamine releasing agent (SNDRA)

    History & Culture

    2-Methylmethcathinone emerged as a novel psychoactive substance during the mid-2010s wave of synthetic cathinone proliferation. The compound was first identified by Swedish authorities in 2014, representing one of the later positional isomers of mephedrone to appear on the recreational drug market. Following its initial detection in Sweden, 2-MMC subsequently spread to other European countries, with reports of its presence emerging from Poland and Spain. As a structural relative of the more widely known mephedrone (4-MMC) and 3-methylmethcathinone (3-MMC), 2-MMC appeared during a period when cathinone derivatives were being systematically explored by clandestine chemists seeking legal alternatives to controlled stimulants. The compound has remained relatively obscure compared to its positional isomers, which gained greater prominence in both recreational use and regulatory attention.

    Effect Profile

    Curated + 4 Reports
    Empathogen 4.7

    Strong sensory enhancement with moderate stimulation, mild euphoria, low empathy

    Empathy / Social Openness×3
    3
    Euphoria / Mood Elevation×2
    5
    Stimulation×1
    6
    Sensory Enhancement×1
    8
    Stimulant 5.5

    Moderate euphoria, anxiety/jitters, and focus with mild stimulation

    Stimulation / Energy×3
    5
    Euphoria / Mood Lift×2
    7
    Focus / Productivity×2
    6
    Anxiety / Jitters×1
    7

    Tolerance & Pharmacokinetics

    drugs.wiki

    Tolerance Decay

    Full tolerance 1h Half tolerance 4d Baseline ~5d

    Experience Report Analysis

    Erowid
    4 Reports
    2016–2025 Date Range
    4 With Age Data
    4 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid

    Effects aggregated from 4 experience reports (4 Erowid)

    4 Reports
    4 Effects Detected
    4 Positive
    0 Adverse
    0 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 4

    Euphoria 75.0% 70%
    Music Enhancement 75.0% 70%
    Focus Enhancement 75.0% 70%
    Stimulation 75.0% 70%

    Adverse Effects 0

    Form / Preparation

    Most common forms and preparations reported

    Legal Status

    Country Status Notes
    Germany NpSG (controlled) Controlled under the Neue-psychoaktive-Stoffe-Gesetz (New Psychoactive Substances Act). Sale, production with intent to sell, and administration to others are criminal offenses. Possession is prohibited but not subject to criminal penalties.
    Poland Illegal (Group I-P) Prohibited as a psychotropic substance under Group I-P. Although not explicitly named in scheduling lists, it is controlled as an isomer of 3-MMC and mephedrone (4-MMC), which are scheduled substances.
    United Kingdom Class B Controlled under the Misuse of Drugs Act 1971. Class B substances carry penalties of up to 5 years imprisonment for possession and up to 14 years for supply or production.
    United States Schedule I Controlled under the Controlled Substances Act as a hallucinogenic substance. Regulated as a positional isomer of mephedrone (4-MMC), which places it automatically under Schedule I classification.
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