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    3-HO-PCP molecular structure

    3-HO-PCP Stats & Data

    3-oh-pcp Hydroxyphencyclidine 3hopcp
    NPS DataHub
    MW259.39
    FormulaC17H25NO
    CAS79787-43-2
    IUPAC3-(1-piperidin-1-ylcyclohexyl)phenol
    SMILESOc1cccc(c1)C1(CCCCC1)N1CCCCC1
    InChIKeyAMSXTZUCNOKUEN-UHFFFAOYSA-N
    Arylcyclohexylamines
    Chemical Class Arylcyclohexylamine
    Psychoactive Class Dissociative

    Receptor Profile

    Receptor Actions

    Agonists
    μ-opioid receptor agonist (partial)
    κ-opioid receptor agonist
    Sigma-1 receptor agonist
    Antagonists
    NMDA receptor antagonist (noncompetitive)

    Receptor Binding

    NMDA antagonist

    History & Culture

    3-HO-PCP was first synthesized in 1978 during investigations into the structure-activity relationships of phencyclidine (PCP) derivatives. Throughout the 1980s, researchers continued to characterize its pharmacological properties, discovering its activity at opioid receptors in animal models during this period. The compound remained largely unknown outside academic circles until 1999, when a chemist operating under the pseudonym "John Q. Beagle" discussed it in a post on The Hive, a now-defunct online chemistry forum. Beagle highlighted the compound's substantially increased potency compared to PCP and its notable affinity for opioid receptors. Even before the substance became commercially available, members of the Bluelight forum had begun documenting its psychoactive effects based on personal experimentation. Around 2009, 3-HO-PCP entered the research chemical market through online vendors. Despite being structurally related to PCP—a compound that had developed considerable notoriety through decades of media coverage and street names like "angel dust," "rocket fuel," and "sherm"—3-HO-PCP has remained one of the more obscure members of the arylcyclohexylamine class. It continues to be distributed primarily through gray-market online sources, with very little formal research having been conducted on its effects, metabolism, or toxicity in humans.

    Toxicity

    PsychonautWiki

    The toxicity and long-term health effects of recreational 3-HO-PCP use have not been studied in any scientific context and the exact toxic dosage is unknown. This is because 3-HO-PCP has an extremely brief history of human usage.

    Effect Profile

    Curated + 12 Reports
    Dissociative 6.6

    Strong dissociative depth with strong motor impairment and mania, moderate insight

    Dissociative Depth×3
    1010
    Mania / Compulsion×1
    8
    Insight / Novel Thought×2
    78.0
    Motor / Sensory Impairment×1
    10
    Catalog BlueLight

    Duration Timeline

    Bluelight
    Onset Comeup Peak Offset After Effects
    Oral
    15-45 minutes
    1-1.5 hours
    2-4 hours
    1-2 hours
    12 hours
    Total: 3-4 hours
    Insufflated
    4-19 minutes
    30 minutes - 1.0 hours
    2-3 hours
    1-2 hours
    12 hours
    Total: 3-4 hours

    Community Effects

    TripSit
    Positive
    stimulation dissociation
    Negative
    nausea tachycardia muscle tension seizures

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Unknown in humans; acute effects suggest hours‑scale persistence with multi‑hour after‑effects.
    Addiction Potential
    Non-medical use shows a notable tendency toward compulsive redosing and binge patterns similar to other PCP-like dissociatives. Frequent/high dosing can lead to tolerance escalation, blackouts, and functional impairment; many users report difficulty moderating use once intoxicated.

    Tolerance Decay

    Full tolerance 2d Half tolerance 7d Baseline ~14d

    Tolerance builds rapidly with repeated use over days and decays over 1–2+ weeks; numbers are approximate and largely anecdotal for this specific analogue.

    Cross-Tolerances

    Ketamine
    3‑MeO‑PCP
    O‑PCE/3‑HO‑PCE

    Experience Report Analysis

    Erowid BlueLight
    17 Reports
    7 Single-substance
    2018–2023 Date Range
    17 With Age Data
    12 Effects Detected

    Demographics

    Gender Distribution

    Too few reports for a chart: gender is known from 17 reports, and a split is drawn only from 20 reports or more. Counts are shown instead. Why 20?

    • Male 11 of 17
    • Not Specified 6 of 17

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid + Bluelight

    Effects aggregated from 12 experience reports (7 single-substance Erowid + 5 Bluelight)

    12 Reports
    50 Effects Detected
    17 Positive
    21 Adverse
    12 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.

    Too few reports for bars: these effects come from 7 single-substance Erowid and 5 analyzed Bluelight 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?

    Positive Effects 17

    Empathy 4 of 7 70%
    Music Enhancement 4 of 7 70%
    Tactile Enhancement 3 of 7 70%
    Euphoria 5 of 12 90%
    Stimulation 2 of 5 80%
    Introspection 2 of 5 82%
    Emotional Openness 1 of 5 80%
    Tinnitus 1 of 5 90%
    Joy 1 of 5 85%
    Mystical Quality 1 of 5 90%
    Revelatory Insight 1 of 5 85%
    Oneness 1 of 5 85%
    Gratitude 1 of 5 85%
    Peace 1 of 5 90%
    Contentment 1 of 5 85%
    Empathogenic Connection 1 of 5 80%
    Insight 1 of 5 90%

    Adverse Effects 21

    Fear 3 of 5 87%
    Confusion 7 of 12 92%
    Motor Impairment 5 of 12 88%
    Vomiting 2 of 5 85%
    Anxiety 4 of 12 90%
    Amnesia 1 of 5 95%
    Dry Mouth 1 of 5 90%
    Involuntary Movements 1 of 5 85%
    Numbness 1 of 5 95%
    Dizziness 1 of 5 90%
    Blurred Vision 1 of 5 85%
    Chills 1 of 5 85%
    Body Temperature Change 1 of 5 80%
    Headache 1 of 5 85%
    Pressure 1 of 5 90%
    Memory Suppression 1 of 5 85%
    Jaw Clenching 1 of 5 75%
    Delusion 1 of 5 95%
    Panic 1 of 5 90%
    Dread 1 of 5 90%
    Show 1 more adverse effect
    Paranoid Ideation 1 of 5 85%
    Show 12 neutral or unclassified mentions
    Dissociation 10 of 12
    Visual Distortions 7 of 12
    Sedation 4 of 7
    Auditory Effects 4 of 7
    Closed-Eye Visuals 3 of 7
    Heaviness 2 of 5
    Deja Vu 2 of 5
    Perceived Size Change 2 of 5
    Near-Death Experience 1 of 5
    Existential Insight 1 of 5
    Thought Loops 1 of 5
    Time Dilation 1 of 5

    Also reported in combinations. In the 10 3-HO-PCP reports where another drug was taken too, 2 mention hospital, emergency services or an overdose, 0 a seizure and 2 psychosis (too few reports for percentages). In the 7 single-substance reports: 0, 0 and 2. These are not in the figures above: they cannot be put down to 3-HO-PCP alone, and a mention is not always something that happened to the writer.

    Real-World Dose Distribution

    Erowid

    From 156 of 160 recorded dose entries: those that state a weight (mg, g or µg), in routes with at least five of them. Values above Q3 + 3×IQR, far above what people typically take, are left out; they can include real heavy doses and overdoses, not only mistakes.

    Oral (n=71)

    Median: 11.0mg 25th: 10.0mg 75th: 15.0mg 90th: 20.0mg

    Rectal (n=69)

    Median: 15.0mg 25th: 11.0mg 75th: 15.0mg 90th: 20.0mg

    Topical (n=5)

    Median: 1.0mg 25th: 1.0mg 75th: 1.0mg 90th: 1.0mg

    Insufflated (n=11)

    Median: 10.0mg 25th: 10.0mg 75th: 13.5mg 90th: 18.0mg

    Common Combinations

    Most co-occurring substances, as a share of all 17 reports filed under 3-HO-PCP

    Too few reports for bars: these combinations come from 17 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?

    • THC 3 of 17

    Form / Preparation

    Most common forms and preparations, as a share of the 13 reports that give one

    Too few reports for bars: these forms come from 13 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?

    • Powder / Crystals 7 of 13
    • Liquid 5 of 13

    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. Doses above Q3 + 3×IQR, far above what people typically take, are left out of the median and range and listed under each route.

    Median: 0.175 mg/kg IQR: 0.152–0.198 mg/kg n=6

    Redose Patterns

    Redosing behavior across 13 reports

    6 of 13 Redosed
    1.9 Avg Doses
    75m 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 7 of 13
    • Redosed 6 of 13

    Legal Status

    Country Status Notes
    Czech Republic Schedule I (List 4) Controlled under Nařízení vlády č. 463/2013 Sb. (§ 1, d), 1.). Permitted for research purposes and restricted therapeutic applications only.
    Germany Unscheduled Not listed as a controlled substance under the Betäubungsmittelgesetz (BtMG). However, under §2 of the Arzneimittelgesetz (AMG), sale for human consumption remains prohibited.
    Sweden Illegal Prohibited substance under Swedish drug control legislation.
    Switzerland Controlled (Verzeichnis E) Specifically named as a controlled substance in Verzeichnis E of Swiss narcotics legislation.
    Turkey Illegal Classified as a controlled drug under Turkish law. Possession, production, supply, and importation are prohibited.
    United Kingdom Class B Controlled under the Misuse of Drugs Act 1971 via the arylcyclohexylamine generic clause introduced by S.I. 2013/239, effective February 26, 2013. As a derivative of 1-phenylcyclohexylamine with a 1-piperidyl group and hydroxy substitution on the phenyl ring, it falls within this catch-all provision. Possession, production, supply, and importation are criminal offenses.

    Harm Reduction

    drugs.wiki

    Potency is high and interindividual variability is large; 1–2 mg can noticeably change effects, so weigh with a calibrated 0.001 g scale or volumetrically. Onset—especially intranasal—can be delayed 40–90+ minutes; redosing during the come‑up is a common trigger for blackouts and hazardous behavior. Several experienced users and moderators note unusually prominent muscle tension/soreness after higher doses; spacing sessions reduces cumulative strain. Intranasal use is often caustic and can inflame sinuses; oral routes are gentler on mucosa. Mislabeling/adulteration has been documented in the wild (e.g., MD‑PiHP sold as 3‑HO‑PCP); use professional drug checking when possible, and do not assume reagent tests can definitively identify PCP analogues. The compound’s opioid receptor profile in vitro is debated; regardless, mixing with CNS depressants increases sedation and slows breathing—avoid these combinations. Dissociatives in general can aggravate mood instability, mania, and psychosis; people with a history of these should avoid or use only with strong support and conservative dosing in a safe setting. Heavy, frequent dissociative use (well‑established for ketamine) is linked to urinary tract problems; while specific data for 3‑HO‑PCP are limited, adopt the same precautions—hydrate, avoid daily use, and stop if urinary symptoms appear. Because ambulation can be preserved while judgment is impaired, trips should be done sitting/lying down with a sober sitter available to prevent accidents.

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