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    4-HO-McPT molecular structure

    4-HO-McPT Stats & Data

    Meprocin 4-hydroxy-mcpt
    NPS DataHub
    MW346.38
    FormulaC18H22N2O5
    IUPAC3-[2-[Cyclopropyl(methyl)amino]ethyl]-1H-indol-4-ol fumarate
    SMILESO=C([O-])C=CC(=O)[O-].CN(CCc1cnc2cccc(O)c12)C1CC1.[H+].[H+]
    InChIKeyQREGQSBVBHZXSR-WLHGVMLRSA-N
    Tryptamines; 2021/5.1 Indol-3-alkylamine; 2022/5.1 Indol-3-alkylamine
    Chemical Class Tryptamine
    Psychoactive Class Psychedelic
    Half-Life Unknown in humans; duration suggests relatively rapid clearance typical of 4-hydroxy tryptamines.

    Receptor Profile

    Receptor Actions

    Agonists
    5-HT2A receptor agonist (full)
    5-HT2C receptor agonist (partial)

    Effect Profile

    Curated + 5 Reports
    Psychedelic 7.1

    Strong visuals and auditory effects with moderate headspace and body load

    Visual Intensity×3
    9
    Headspace Depth×3
    6
    Auditory Effects×1
    8
    Body Load / Somatic Effects×1
    6

    Duration Timeline

    Bluelight
    Onset Comeup Peak Offset After Effects
    Oral
    19-40 minutes
    30 minutes - 1.0 hours
    2-3 hours
    1-2 hours
    1-3 hours
    Insufflated
    4-15 minutes
    15-30 minutes
    45 minutes - 1.5 hours
    30 minutes - 1.0 hours
    1-2 hours
    Smoked
    1-3 minutes
    10-30 minutes
    15-45 minutes
    1-6 hours

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Unknown in humans; duration suggests relatively rapid clearance typical of 4-hydroxy tryptamines.
    Addiction Potential
    Low; classical 4-substituted tryptamines have low habit-forming liability.

    Tolerance Decay

    Full tolerance 1d Half tolerance 3d Baseline ~7d

    Pattern extrapolated from classical psychedelic tolerance: marked within 24 h, decreases substantially by 3–4 days, and approximates baseline after ~7–14 days. Data are indirect and rely on broader psychedelic literature and user reports rather than 4-HO-McPT-specific studies.

    Cross-Tolerances

    Psilocybin/Psilocin
    50% ●○○
    Other 4-substituted tryptamines (e.g., 4-HO-MiPT, 4-HO-MET)
    50% ●○○
    LSD
    30% ●○○

    Experience Report Analysis

    Erowid
    5 Reports
    2016–2021 Date Range
    5 With Age Data
    5 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid

    Effects aggregated from 5 experience reports (5 Erowid)

    5 Reports
    5 Effects Detected
    3 Positive
    0 Adverse
    2 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 3

    Color Enhancement 80.0% 70%
    Stimulation 60.0% 70%
    Empathy 60.0% 70%

    Adverse Effects 0

    Real-World Dose Distribution

    62K Doses

    From 5 individual dose entries

    Form / Preparation

    Most common forms and preparations reported

    Harm Reduction

    drugs.wiki

    Extremely limited human data exist for 4-HO-McPT; treat all dose and duration guidance as tentative and titrate cautiously with a milligram scale. Anecdotal reports suggest a relatively brief and sometimes wave-like course orally, with some users noting mild rebound headaches; plan set, setting, and next-day commitments accordingly. Given the scarcity of pharmacokinetic data, avoid redosing quickly, as delayed absorption or batch variability could cause unexpectedly strong effects. Several users describe severe nasal burn and irritation with insufflation; oral use is the least caustic known route and is the default for most 4-hydroxy tryptamines. As with other serotonergic psychedelics, avoid combining with lithium due to a substantially increased seizure risk observed when classic psychedelics are taken with lithium; this applies even at therapeutic lithium levels. MAOIs can markedly potentiate tryptamines and increase risks (e.g., hypertensive reactions and serotonin toxicity), so this combination should be strictly avoided outside clinical settings. Tramadol lowers seizure threshold and has serotonergic activity; combining with psychedelics increases seizure and adverse neuropsychiatric risk and should be avoided. Stimulants (e.g., amphetamines, cocaine) can amplify anxiety, cardiovascular strain, and thought loops; avoid or use extreme caution if you have any cardiovascular, anxiety, or panic history. SSRIs/SNRIs often blunt the subjective effects of psychedelics but can still interact unpredictably; if on antidepressants, avoid DIY discontinuation and consult a clinician instead of mixing. Because unregulated markets frequently mislabel tryptamines (e.g., 4-HO-MET sold as psilocybin), use accredited drug checking where available, recognizing that at-home reagents are helpful but not definitive. Perform a low-dose allergy test with any new batch and use accurate scales; start at threshold if untested. Individuals with a personal or family history of seizures, serious cardiovascular disease, or current manic states should avoid experimental tryptamines like 4-HO-McPT. Have a sober, trusted sitter for first trials, avoid alcohol or sedatives to “manage” the trip, and seek medical help promptly for severe agitation, chest pain, uncontrolled vomiting, loss of consciousness, or convulsions.

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