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    4-AcO-MET molecular structure

    4-AcO-MET Stats & Data

    Metacetin 4-acetoxy-met O-acetylmetocin 4acomet
    NPS DataHub
    MW260.34
    FormulaC15H20N2O2
    CAS1445751-40-5
    IUPAC3-(2-Ethyl(methyl)aminoethyl)-1''H''-indol-4-yl acetate
    SMILESCCN(C)CCc1cnc2cccc(OC(C)=O)c12
    InChIKeyOMDKHOOGGJRLLX-UHFFFAOYSA-N
    Tryptamines; 2020/5.1 Indol-3-alkylamine; 2021/5.1 Indol-3-alkylamine; 2022/5.1 Indol-3-alkylamine
    Chemical Class Substituted tryptamine
    Psychoactive Class Psychedelic

    History & Culture

    4-AcO-MET, also known as metacetin, is a novel synthetic tryptamine that emerged primarily through the online research chemical market. As an acetate ester of 4-HO-MET and a structural homologue of 4-AcO-DMT, it represents one of many acetylated tryptamine derivatives that have been synthesized and distributed in recent decades. The compound has very little documented history of human use compared to more established psychedelics. Unlike substances such as psilocybin or LSD, which have decades of clinical research and cultural significance, 4-AcO-MET remains relatively obscure with minimal data regarding its pharmacological properties, metabolism, or toxicity profile. Its availability has been primarily limited to online research chemical vendors, where it is marketed alongside other novel tryptamine analogues.

    Subjective Effects

    Physical

    The physical effects of 4-AcO-MET can be broken down into three components all of which progressively intensify proportional to dosage.

    • Spontaneous tactile sensations: The 'body high' of 4-AcO-MET can be described as a pleasurable, warm, soft and all-encompassing tingling sensation. This maintains a consistent presence that steadily rises with the onset and hits its limit once the peak has been reached.
    • Sedation: In terms of its effects on the physical energy levels of the tripper, 4-AcO-MET is considered by most to be relaxing, stoning and mildly sedating. This sense of sedation is often accompanied by compulsive yawning.
    • Nausea
    Cognitive

    The cognitive effects of 4-AcO-MET are described by many as somewhat relaxing, yet fast-paced in style with similarities to psychedelics such as LSD or 2C-B which tend to be cognitively energetic and stimulating.

    • Enhancement of current mind state
    • Connectivity of thought
    • Acceleration of thought
    • Feelings of fascination, importance and awe
    • Time distortion
    • Outrospection
    • Thought loops
    • Removal of cultural filter
    • Conceptual thinking
    • Direct communication with the subconscious
    • Ego suppression, loss and death
    • Feelings of interdependent opposites
    • Delusions
    • States of unity and interconnectedness
    Sensory
    Auditory
    • Enhancements
    • Distortions
    • Hallucinations
    Visual · Distortions
    • Visual drifting: (Melting, Flowing, Breathing and morphing) - In comparison to other psychedelics, this effect can be described as highly detailed, cartoon-like in style, slow and smooth in motion and static in appearance.
    • Tracers
    • After images
    • Texture repetition
    • Colour shifting
    • Scenery slicing
    Visual · Enhancements
    • Increased visual acuity
    • Enhancement of colour
    • Enhanced pattern recognition
    Visual · Hallucinatory States

    4-AcO-MET and its various other forms produce a full range of high level hallucinatory states in a fashion that is more consistent and reproducible than that of many other commonly used psychedelics.

    • Transformations
    • Internal hallucinations: (Autonomous entities, Settings, sceneries, and landscapes, Alterations in perspective and Scenarios and plots) - This effect is very consistent in dark environments at appropriately high dosages. They can be comprehensively described through their variations as lucid in believability, interactive in style, new experiences in content, autonomous in controllability, geometry-based in style and almost exclusively of a religious, spiritual, mystical, science fiction or transcendental nature in overall theme.

    Forked from Subjective Effect Documentation by Josie Kins, August 2014. Via dose.wiki (CC0).

    Toxicity

    PsychonautWiki

    The toxicity and long-term health effects of recreational 4-AcO-MET use do not seem to have been studied in any scientific context and the exact toxic dose is unknown. This is because 4-AcO-MET is a research chemical with very little history of human usage. Anecdotal evidence suggests that there are no negative health effects attributed to simply trying the drug by itself at low to moderate doses and using it very sparingly (but nothing can be completely guaranteed). Independent research should always be done to ensure that a combination of two or more substances is safe before consumption. It is strongly recommended that one use harm reduction practices when using this substance.

    Effect Profile

    Curated + 20 Reports
    Psychedelic 9.2

    Strong visuals, headspace, and auditory effects with moderate body load

    Visual Intensity×3
    107.5
    Headspace Depth×3
    102.6
    Auditory Effects×1
    102.6
    Body Load / Somatic Effects×1
    63.4
    Catalog BlueLight

    Tolerance & Pharmacokinetics

    drugs.wiki

    Tolerance Decay

    Full tolerance 1h Half tolerance 10d Baseline ~14d

    Cross-Tolerances

    LSD
    Psilocybin
    Psilocin
    Mescaline
    DMT
    5-MeO-DMT
    2C-B
    2C-E

    Experience Report Analysis

    Erowid BlueLight
    23 Reports
    7 Single-substance
    2013–2025 Date Range
    21 With Age Data
    12 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid + Bluelight

    Effects aggregated from 20 experience reports (7 single-substance Erowid + 13 Bluelight)

    20 Reports
    87 Effects Detected
    50 Positive
    24 Adverse
    13 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Each bar is the share of reports mentioning the effect; its whisker, and the band on the rows below, is the 95% interval: where the share could plausibly be with other reports of the same kind.

    Rows resting on fewer than 20 reports show a count (“3 of 7”) instead of a bar. Why 20?

    Positive Effects 50

    Color Enhancement 60.0% (95% interval 39 to 78 percent) 89%
    Closed-Eye Visuals 55.0% (95% interval 34 to 74 percent) 92%
    Euphoria 45.0% (95% interval 26 to 66 percent) 89%
    Music Enhancement 40.0% (95% interval 22 to 61 percent) 88%
    Introspection 40.0% (95% interval 22 to 61 percent) 82%
    Visual Distortions 7 of 7 70%
    Open-Eye Visuals 11 of 13 90%
    Stimulation 5 of 7 70%
    Patterning 7 of 13 87%
    Empathy 3 of 7 70%
    Entity Imagery 5 of 13 86%
    Geometric Imagery 5 of 13 88%
    Contentment 5 of 13 78%
    Joy 4 of 13 89%
    Morphing 4 of 13 86%
    Surface Breathing 4 of 13 84%
    Warping 3 of 13 85%
    Awe 3 of 13 83%
    Peace 3 of 13 82%
    Fractal Imagery 2 of 13 88%

    Adverse Effects 24

    Anxiety 40.0% (95% interval 22 to 61 percent) 83%
    Muscle Tension 20.0% (95% interval 8 to 42 percent) 75%
    Increased Heart Rate 3 of 7 70%
    Thought Disorganization 4 of 13 76%
    Body Load 3 of 13 78%
    Chills 3 of 13 77%
    Nausea 2 of 13 88%
    Thought Acceleration 2 of 13 78%
    Confusion 2 of 13 85%
    Fear 2 of 13 75%
    Insomnia 2 of 13 82%
    Dysphoria 2 of 13 78%
    Headache 1 of 13 80%
    Sweating 1 of 13 75%
    Pressure 1 of 13 80%
    Memory Suppression 1 of 13 80%
    Focus Suppression 1 of 13 85%
    Panic 1 of 13 75%
    Paranoid Ideation 1 of 13 85%
    Temporal Disorientation 1 of 13 85%
    Show 4 more adverse effects
    Regret 1 of 13 85%
    Sadness 1 of 13 80%
    Disrupted Sleep Architecture 1 of 13 75%
    Contrast Enhancement 1 of 13 80%

    Dosage Distribution

    Dose distribution from experience reports, one dose per report (the first listed). Values above Q3 + 3×IQR are left out as outliers.

    Median: 20.0 mg IQR: 14.5–30.0 mg n=12 1 outlier left out

    Real-World Dose Distribution

    62K Doses

    From 44 individual dose entries. Values above Q3 + 3×IQR are left out as outliers.

    Oral (n=38)

    Median: 22.5mg 25th: 13.5mg 75th: 31.5mg 90th: 40.0mg

    Common Combinations

    Most co-occurring substances, as a share of all 23 reports filed under 4-AcO-MET; whiskers are 95% intervals

    Form / Preparation

    Most common forms and preparations, as a share of the 11 reports that give one

    Too few reports for bars: these forms come from 11 reports, and a bar is drawn only from 20 reports or more. With fewer, a percentage cannot tell a common effect from a rare one. Counts are shown instead. Why 20?

    • Capsule 6 of 11
    • Powder / Crystals 5 of 11

    Body-Weight Dosing

    Dose per kg of body weight, one dose per report (the first listed), from reports giving a weight of 30–250 kg. Values above Q3 + 3×IQR are left out as outliers.

    Median: 0.284 mg/kg IQR: 0.22–0.508 mg/kg n=13

    Redose Patterns

    Redosing behavior across 13 reports

    2 of 13 Redosed
    1.3 Avg Doses
    60m Median Interval

    Too few reports for a chart: redosing is known from 13 reports, and a split is drawn only from 20 reports or more. Counts are shown instead. Why 20?

    • Single dose 11 of 13
    • Redosed 2 of 13

    Legal Status

    Country Status Notes
    Germany NpSG (Controlled) Controlled under the Neue-psychoaktive-Stoffe-Gesetz (New Psychoactive Substances Act) as of July 18, 2019. Production, import with intent to market, administration to others, and trading are punishable offenses. Possession is illegal but not subject to criminal penalty. Ordering may potentially constitute incitement to place on the market.
    Switzerland Controlled (Verzeichnis E) Specifically named as a controlled substance under Verzeichnis E of Swiss narcotics legislation.
    United Kingdom Class A Controlled as a Class A substance under the Misuse of Drugs Act 1971. Classification stems from being an ester of 4-HO-MET, which itself is controlled under the tryptamine catch-all clause.
    United States Unscheduled Not specifically scheduled under the Controlled Substances Act. However, as a structural analogue of psilocin (a Schedule I substance), sale for human consumption or use for illicit non-medical purposes could potentially be prosecuted under the Federal Analogue Act.
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