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    4-MTA molecular structure

    4-MTA Stats & Data

    Mta Flatliners Golden eagle 4-methylthioamphetamine
    NPS DataHub
    MW217.76
    FormulaC10H16ClNS
    CAS94784-92-6
    SMILES[Cl-].CSc1ccc(cc1)CC(C)N.[H+]
    InChIKeyDGCZWGSFSFNXNS-UHFFFAOYSA-N
    Phenethylamines; 2020/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2021/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2022/1. Von 2-Phenethylamin abgeleitete Verbindungen
    Chemical Class Amphetamine
    Psychoactive Class Psychedelic / Stimulant
    Half-Life Unknown in humans; prolonged functional duration likely reflects both releasing action and MAO-A inhibition.

    Pharmacology

    DrugBank
    State Solid

    Effect Profile

    Curated + 2 Reports
    Psychedelic 3.0

    Moderate body load with mild visuals, low headspace

    Visual Intensity×3
    5
    Headspace Depth×3
    2
    Auditory Effects×1
    0
    Body Load / Somatic Effects×1
    7
    Empathogen 5.0

    Moderate stimulation and sensory enhancement with mild empathy, low euphoria

    Empathy / Social Openness×3
    5
    Euphoria / Mood Elevation×2
    3
    Stimulation×1
    7
    Sensory Enhancement×1
    7
    Stimulant 3.6

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

    Stimulation / Energy×3
    5
    Euphoria / Mood Lift×2
    3
    Focus / Productivity×2
    4
    Anxiety / Jitters×1
    10

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Unknown in humans; prolonged functional duration likely reflects both releasing action and MAO-A inhibition.
    Addiction Potential
    Low compulsive-use liability relative to dopaminergic stimulants, but a narrow safety margin and severe, sometimes fatal serotonergic toxicity make any repeated use extremely dangerous.

    Tolerance Decay

    Full tolerance 0h Half tolerance 0d Baseline ~7d

    Human tolerance kinetics are poorly documented due to rarity and high lethality; assume some acute tolerance with slow recovery over days, and significant pharmacodynamic carryover for at least 24–48 h post-use.

    Cross-Tolerances

    MDMA (and other serotonin-releasing entactogens)
    50% ●○○

    Experience Report Analysis

    Erowid
    2 Reports
    2001–2004 Date Range
    1 With Age Data

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Real-World Dose Distribution

    62K Doses

    From 1 individual dose entries

    Harm Reduction

    drugs.wiki

    4-MTA is a potent serotonin-releasing agent with additional MAO-A–inhibiting activity; this dual action is strongly linked to severe hyperthermia and serotonin toxicity seen in clusters of 1997–1999 European cases. The EU risk assessment emphasized a slow onset and long-lasting effects that promoted redosing and overdoses, especially when mis-sold as MDMA. Because 4-MTA can functionally inhibit MAO-A, combining it with serotonergic medications (SSRIs/SNRIs/TCAs), other recreational serotonergics (MDMA, PMA/PMMA, DXM, tramadol), or tyramine-rich foods can precipitate dangerous hypertensive or serotonin syndromes. Historical harm data include multiple deaths; some were associated with pills sold as 'ecstasy' where users re-dosed due to delayed onset. Avoid all combinations and redosing; the safest choice is to not use at all. If someone has taken it, active cooling (shade, fans, loosening clothing), fluids with electrolytes, and rapid medical evaluation are critical at the first signs of serotonin toxicity (agitation, confusion, tremor/hyperreflexia, clonus, sweating, temperature rising). Do not rely on antipyretics alone and do not self-treat severe agitation with alcohol or polypharmacy. Expect effects to persist all day or longer; avoid any serotonergic agent for at least 24–48 hours after exposure due to lingering pharmacologic effects. Because 4-MTA has been misrepresented in tablets, reagent tests may not reliably identify it; if using any pressed pill or powder, drug-checking with laboratory-grade services is far safer than color reagents. Warm, crowded environments and prolonged dancing markedly increase hyperthermia risk; rest often, pre-plan cooling, and have a sober sitter who can call emergency services if symptoms escalate. Early hospital care saves lives; tell clinicians exactly what was taken to guide management (e.g., benzodiazepine sedation, aggressive cooling).

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