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    4-Me-TMP molecular structure

    4-Me-TMP Stats & Data

    4-mmph 4-metmp 4-methylmethylphenidate
    NPS DataHub
    MW247.34
    FormulaC15H21NO2
    CAS191790-79-1
    IUPACmethyl 2-(4-methylphenyl)-2-piperidin-2-ylacetate
    SMILESCOC(=O)C(C1CCCCN1)c1ccc(C)cc1
    InChIKeyWJZNCJIOIACDBR-UHFFFAOYSA-N
    Phenethylamines; Piperidines & pyrrolidines; 2020/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2021/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2022/1. Von 2-Phenethylamin abgeleitete Verbindungen
    Psychoactive Class Stimulant
    Half-Life Estimated 2–4 hours (human data sparse; inference from class and reported duration).

    History & Culture

    4-Methylmethylphenidate emerged on the designer stimulant market in mid-2015, appearing shortly after regulatory actions in the United Kingdom restricted ethylphenidate and other phenidate compounds. Its commercial availability as an unscheduled research chemical proved exceptionally brief, lasting only several months before facing its own regulatory restrictions. Beyond its brief presence on the grey market, the compound has attracted interest in formal research settings. Its distinctive pharmacological profile prompted investigation as a potential substitute medication for the treatment of stimulant use disorders.

    Effect Profile

    Curated
    Stimulant 4.6

    Strong anxiety/jitters and euphoria with mild focus, low stimulation

    Stimulation / Energy×3
    3
    Euphoria / Mood Lift×2
    9
    Focus / Productivity×2
    5
    Anxiety / Jitters×1
    10

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Estimated 2–4 hours (human data sparse; inference from class and reported duration).
    Addiction Potential
    Anecdotally similar to other phenidate stimulants: psychological dependence risk, especially with frequent redosing or high doses; binges reported by some users, while others note low recreational pull.

    Tolerance Decay

    Full tolerance 3d Half tolerance 7d Baseline ~14d

    Patterns extrapolated from user reports with methylphenidate-class stimulants: tolerance can build across several days of repeated use and may require 1–2 weeks to substantially reset. Data quality is low and highly individual.

    Cross-Tolerances

    methylphenidate
    60% ●○○
    ethylphenidate
    50% ●○○
    other phenidates
    40% ●○○

    Legal Status

    Country Status Notes
    United Kingdom Temporary Class Drug Designated as a Temporary Class Drug beginning in June 2015 following its unapproved sale as a designer drug. This classification prohibits importation, exportation, production, and supply of the substance.
    United States Unscheduled (Federal Analogue Act may apply) Not explicitly scheduled at the federal level, but may be treated as a controlled substance under the Federal Analogue Act when intended for human consumption due to its structural relationship to methylphenidate. A September 2023 DEA proposal to place ethylphenidate into Schedule I would encompass its positional isomers, including this compound.

    Harm Reduction

    drugs.wiki

    Identity and purity in the current supply are uncertain; drug checking is strongly advised because mislabeling and unexpected contents in powders/crystals are common in unregulated markets. Start with a low single dose, wait at least 2 hours before considering any redose, and avoid stacking multiple redoses to reduce cardiac and insomnia risks. As with methylphenidate analogs, expect dose‑dependent increases in heart rate, blood pressure, anxiety, jaw tension, and appetite suppression; those with cardiovascular or anxiety disorders should exercise heightened caution. Intranasal use can damage nasal mucosa over time; divide lines finely, use each nostril sparingly, rinse with saline after sessions, and avoid sharing equipment to reduce infection risk. Avoid injecting; if someone is intent on IV use, sterile technique, allergy testing with a tiny fraction dose, and filtration are essential to reduce acute harms from insoluble binders or contaminants. Combining with MAOIs is hazardous due to hypertensive events; avoid this combination entirely. Tramadol plus stimulants can lower seizure threshold and increase serotonin toxicity risk; avoid co‑use and space by many half‑lives if medically required. Stimulant comedowns can be mitigated with sleep hygiene, fluids, electrolytes, gentle nutrition, and time; avoid chasing sleep with high‑dose alcohol or benzodiazepines due to masking/overdose risk. Because potency appears lower than methylphenidate for many, there is a temptation to escalate doses; use a calibrated milligram scale, consider volumetric solutions for accurate micro‑titration, and cap the session length before starting. Insomnia is common after late‑day dosing; avoid use within 8–12 hours of planned sleep. Cross‑tolerance with other phenidates is likely; leave sufficient spacing (several days or longer) between sessions to reduce tolerance and binge‑cycle risk. Little formal human pharmacokinetic/toxicology data exists for 4‑Me‑TMP; absence of data is not evidence of safety—use conservative dosing and vigilant self‑monitoring.

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