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    Chemical Class Amphetamine
    Psychoactive Class Psychedelic / Stimulant
    Half-Life Unknown in humans; long duration suggests prolonged elimination but no human PK studies have established an actual half-life.

    Pharmacology

    DrugBank

    Metabolism

    21-hydroxy-progesterone is a known human metabolite of progesterone.

    Receptor Profile

    Receptor Actions

    Agonists
    5-HT2A receptor agonist (partial)
    5-HT2B receptor agonist (partial)
    5-HT2C receptor agonist (partial)

    Receptor Binding

    5-HT 2C partial agonist

    History & Culture

    1972–1973

    DOC was originally synthesized by Ronald Coutts and Jerry Malicky at the University of Alberta in Canada. Their work describing the compound was published in the scientific literature in 1973 as part of research into analogues of DOM and related substituted amphetamines. The substance remained largely obscure for nearly two decades following its initial synthesis.

    1989–1991

    Prior to becoming widely known, DOC appeared in forensic analysis of designer amphetamine samples, with the compound being identified in Canadian drug seizures as early as 1989. Human usage was subsequently popularized following the 1991 publication of PiHKAL (Phenethylamines I Have Known And Loved) by Alexander Shulgin, which provided detailed information on the compound's synthesis and pharmacological effects. Shulgin characterized DOC as an "archetypical psychedelic" with pronounced effects, noting that everything is present "in spades" compared to the more subtle qualities of related two-carbon phenethylamines.

    2005–present

    DOC has remained uncommon on traditional illicit drug markets, instead circulating primarily through online research chemical vendors operating in legal grey areas. Sales of DOC distributed on blotting paper and in capsule form were reported in late 2005 and again in late 2007. The compound's availability in blotter format has led to instances of misrepresentation, with DOC sometimes being sold as LSD by unscrupulous dealers. A notable example occurred in December 2007 when police in Contra Costa County, California seized blotter paper suspected to be LSD that laboratory analysis revealed to contain DOC instead.

    Effect Profile

    Curated + 148 Reports
    Psychedelic 8.1

    Strong visuals, body load, headspace, and auditory effects

    Visual Intensity×3
    10102.9
    Headspace Depth×3
    9102.1
    Auditory Effects×1
    8100.8
    Body Load / Somatic Effects×1
    10103.6
    Catalog Erowid BlueLight
    Stimulant 8.0

    Strong stimulation, euphoria, and anxiety/jitters with moderate focus

    Stimulation / Energy×3
    1010
    Euphoria / Mood Lift×2
    106.9
    Focus / Productivity×2
    76.5
    Anxiety / Jitters×1
    1010
    Catalog Erowid

    Duration Timeline

    Bluelight
    Onset Comeup Peak Offset After Effects
    Oral
    45 minutes - 2.0 hours
    1-2.5 hours
    3.5-6 hours
    3-6 hours
    6-48 hours
    Total: 10-20 hours
    Insufflated
    0-6 minutes
    12-30 minutes
    2-6 hours
    2-8 hours
    2-24 hours
    Total: 10-20 hours

    Empirical Duration

    Erowid Reports
    Onset Come Up Peak Offset
    Oral (25 reports)

    Community Effects

    TripSit
    Positive
    visual enhancement euphoria stimulation color enhancement introspection
    Negative
    vasoconstriction body load insomnia anxiety

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Unknown in humans; long duration suggests prolonged elimination but no human PK studies have established an actual half-life.
    Addiction Potential
    Low; not considered physically addictive, but psychological habituation is possible with frequent use.

    Tolerance Decay

    Full tolerance 1d Half tolerance 7d Baseline ~14d

    Tolerance to DOC (and classic psychedelics) rises sharply after an experience and then decays over about 1–2 weeks; model and ratios are heuristic, inferred from user reports, not measured pharmacology.

    Cross-Tolerances

    LSD
    70% ●○○
    DOM
    70% ●○○
    DOB
    80% ●○○

    Experience Report Analysis

    Erowid BlueLight
    83 Reports
    2005–2022 Date Range
    44 With Age Data
    33 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid + Bluelight

    Effects aggregated from 133 experience reports (83 Erowid + 65 Bluelight)

    133 Reports
    139 Effects Detected
    64 Positive
    50 Adverse
    25 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 64

    Stimulation 57.1% 85%
    Color Enhancement 54.9% 85%
    Music Enhancement 40.6% 89%
    Euphoria 39.9% 88%
    Awe 30.0% 80%
    Empathy 28.6% 80%
    Visual Trails 28.0% 84%
    Thought Acceleration 28.0% 81%
    Body High 24.1% 84%
    Introspection 24.1% 80%
    Tactile Enhancement 22.5% 90%
    Morphing 22.0% 84%
    Focus Enhancement 21.8% 80%
    Geometric Imagery 18.0% 85%
    Joy 16.0% 86%
    Contentment 14.0% 81%
    Patterning 14.0% 81%
    Surface Breathing 10.0% 80%
    Insight 10.0% 80%
    Entity Imagery 10.0% 78%

    Adverse Effects 50

    Anxiety 45.1% 76%
    Confusion 30.1% 82%
    Body Load 30.0% 77%
    Nausea 26.3% 80%
    Muscle Tension 21.8% 75%
    Pupil Dilation 17.3% 85%
    Fear 12.0% 81%
    Insomnia 12.0% 82%
    Psychosis 10.8% 70%
    Memory Suppression 10.6% 80%
    Thought Disorganization 10.0% 78%
    Jaw Clenching 9.0% 82%
    Headache 9.0% 78%
    Increased Heart Rate 8.4% 70%
    Motor Impairment 8.2% 75%
    Dysphoria 8.0% 78%
    Depersonalization 8.0% 76%
    Vomiting 8.0% 88%
    Seizure 6.0% 70%
    Sweating 6.0% 85%

    Dose-Response Correlation

    How effect frequency changes across dose levels

    View data table
    Effect Common (n=19)
    Visual Distortions 84.2%
    Music Enhancement 73.7%
    Stimulation 73.7%
    Confusion 68.4%
    Anxiety 63.2%
    Color Enhancement 63.2%
    Euphoria 57.9%
    Empathy 57.9%
    Sedation 57.9%
    Pupil Dilation 42.1%
    Muscle Tension 36.8%
    Tactile Enhancement 36.8%
    Focus Enhancement 36.8%
    Dissociation 31.6%
    Body High 31.6%

    Dose–Effect Mapping

    Experience Reports

    How reported effects shift across dose tiers, based on 83 experience reports.

    Limited tier coverage — most reports fall within the Common range. Effects at other dose levels may not be represented.

    Oral dose range: 2.2–5.0 mg (median 3.0 mg)
    Effect Common (n=19)
    visual distortions
    84%
    music enhancement
    74%
    stimulation
    74%
    confusion
    68%
    anxiety
    63%
    color enhancement
    63%
    euphoria
    58%
    empathy
    58%
    sedation
    58%
    pupil dilation
    42%
    muscle tension
    37%
    tactile enhancement
    37%
    focus enhancement
    37%
    dissociation
    32%
    body high
    32%
    auditory effects
    32%
    closed-eye visuals
    32%
    nausea
    32%
    introspection
    26%
    ego dissolution
    21%

    Showing top 20 of 27 effects

    Dosage Distribution

    Dose distribution from experience reports

    Median: 3.0 mg IQR: 2.2–5.0 mg n=36

    Real-World Dose Distribution

    62K Doses

    From 118 individual dose entries

    Oral (n=71)

    Median: 3.0mg 25th: 2.0mg 75th: 3.65mg 90th: 5.0mg
    mg/kg median: 0.04 mg/kg 75th: 0.059

    Insufflated (n=8)

    Median: 2.88mg 25th: 1.0mg 75th: 3.25mg 90th: 4.0mg
    mg/kg median: 0.034 mg/kg 75th: 0.044

    Common Combinations

    Most co-occurring substances in experience reports

    Form / Preparation

    Most common forms and preparations reported

    Body-Weight Dosing

    Dose relative to body weight from reports with weight data

    Median: 0.04 mg/kg IQR: 0.03–0.063 mg/kg n=36

    Redose Patterns

    Redosing behavior across 63 reports

    12.7% Redosed
    1.2 Avg Doses
    240m Median Interval

    Legal Status

    UN Convention on Psychotropic Substances 1971 (Schedule II, added March 2020)
    Country Status Notes
    Austria Controlled (NPSG) Prohibited under the Neue-Psychoaktive-Substanzen-Gesetz (New Psychoactive Substances Act). Possession, production, and sale are illegal without authorization.
    Brazil Controlled Listed on Portaria SVS/MS nº 344. Possession, production, and sale are prohibited.
    Canada Schedule I CDSA Controlled under the Controlled Drugs and Substances Act. Additionally covered by the 2016 regulation controlling phenethylamines with a 2,5-dimethoxyphenylethamine core structure. Illegal to sell, buy, or possess without valid legal exemption.
    China Category I psychotropic substance Controlled since October 2015. Illegal to sell, buy, import, export, or manufacture without authorization.
    Denmark Schedule I Added to the list of Schedule I controlled substances as of April 8, 2007, alongside 2C-E, 2C-P, and DOI.
    Finland Controlled Possession, production, and sale are prohibited under national drug legislation.
    Germany Anlage I BtMG Listed in Anlage I of the Betäubungsmittelgesetz (Narcotics Act) since February 1, 1997. Manufacturing, possession, importation, exportation, purchase, sale, procurement, and dispensing are all prohibited without a license.
    Israel Controlled Possession, production, and sale are prohibited under national drug legislation.
    Latvia Schedule I Classified as a Schedule I controlled substance under Latvian law.
    Netherlands Controlled Possession, production, and sale are prohibited under the Opium Act.
    New Zealand Class C Controlled as an amphetamine analogue under Schedule III (Class C) of New Zealand's controlled substances legislation.
    Poland Uncontrolled As of 2011, DOC was not a controlled substance and no analogue law covered it. Current status may have changed.
    Switzerland Controlled (Verzeichnis E) Regulated as a defined derivative of α-methylphenethylamine under Verzeichnis E point 130. Permitted for scientific or industrial purposes only.
    Turkey Controlled Classified as a controlled drug. Illegal to possess, produce, supply, or import.
    United Kingdom Class A Controlled under the Misuse of Drugs Act 1971 through the amphetamine analogue clause. Class A/Schedule I classification prohibits sale, purchase, and possession without a license.
    United States Unscheduled (Federal Analogue Act applies) Not federally scheduled, but may be prosecuted as an analogue of DOM or DOB under the Federal Analogue Act when sold for human consumption or possessed with intent to ingest. Specifically listed as Schedule I in Florida state law.

    Harm Reduction

    drugs.wiki

    DOC is a potent psychedelic amphetamine with a slow onset and very long duration; because onset may take 2–3 hours, redosing early greatly increases the risk of accidental overdose and an excessively long experience. Verified drug-checking programs have repeatedly found DOC sold as LSD on blotter; when ingesting unknown blotter, wait at least 3 hours before redosing, ideally after reagent/lab testing, to avoid stacking doses of a long-acting compound. DOC can cause peripheral vasoconstriction and stimulant-like effects (elevated heart rate/blood pressure, chest tightness) especially at higher doses; those with cardiovascular disease or hypertension should avoid it and all users should avoid combining with other vasoconstrictors (stimulants, decongestants, high-dose caffeine). Lithium has been repeatedly associated with seizures and severe adverse reactions when combined with classic psychedelics; treat this combination as dangerous and avoid it. Mixing with MAOIs is also considered dangerous due to unpredictable potentiation and hypertensive risk; tramadol adds seizure risk and serotonergic toxicity potential. If acute anxiety or dysphoria occur, non-pharmacological de-escalation (calm environment, breathing, reassurance) is first-line; benzodiazepines can attenuate the experience but should not be combined with alcohol or other depressants due to additive sedation and respiratory depression. Because activity is in the low-milligram range, use a calibrated milligram scale or volumetric dosing; never eyeball powder. DOC commonly disrupts sleep; plan for next-day impairment and avoid driving or operating machinery during and after effects. Tolerance builds rapidly after one dose and substantially reduces effects for about 1–2 weeks; cross-tolerance exists with other serotonergic psychedelics (e.g., LSD, DOB/DOM). Human pharmacokinetic data (including elimination half-life) are not established; reported half-life figures online are estimates inferred from long duration rather than measured studies, so dose-spacing and conservative titration are essential. Drug checking (reagent and, where available, lab confirmation) is strongly recommended for any blotter or liquid purported to be LSD given frequent mislabeling with DOx compounds in some markets.

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