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3-MeO-PCP (3-methoxyphencyclidine) is a dissociative new psychoactive substance of the arylcyclohexylamine (phencyclidine) class. It acts principally as an antagonist at the N-methyl-D-aspartate (NMDA) glutamate receptor and is additionally reported to inhibit monoamine reuptake, giving it a more stimulating and dopaminergic character than ketamine; the closely related analogs 4-MeO-PCP and 3-MeO-PCMo have been shown to engage the mesolimbic dopamine pathway to produce rewarding and reinforcing effects. It is considerably more potent and longer-acting than ketamine, which contributes to a narrow margin between recreational and toxic exposure. The compound has been implicated in numerous non-fatal intoxications and deaths, and its metabolism and analytical detection have been characterized in forensic casework and in silico ADME studies. Because standard phencyclidine immunoassays detect it inconsistently, laboratory confirmation generally relies on chromatographic and mass-spectrometric methods.
- NMDA-antagonist dissociative
- More stimulating than ketamine
- Potent, long-acting NMDA receptor antagonist
- Narrow margin; easy to overshoot
- Agitation, high blood pressure, mania-like or psychotic states
- Strong potential for compulsive redosing
Mechanism
3-MeO-PCP is an ; by blocking this channel it produces the detached, anesthetic dissociative state. Compared with ketamine it has more -transporter and sigma activity, giving a more stimulating, longer, and more variable experience. That extra dopaminergic push is part of why it carries a higher risk of agitation, mania-like states, and compulsive redosing.
receptor fingerprint
antagonist
reuptake inhibitor
Sigma receptorsagonist
Safetyrisks and cautions, not medical advice
This is one of the riskier dissociatives; the gap between a manageable and an overwhelming amount is narrow, and higher exposure can bring dangerous agitation, high blood pressure, and psychosis-like states, with a real potential for compulsive redosing. It stacks dangerously with other depressants (sedation/breathing) and with stimulants (cardiac and psychological strain). Treat it with a lot of caution; not medical advice.
Subjective profileweighing the evidence above
One of the riskier dissociatives around, and the risk is structural: a steep dose curve, a long duration, and a strong pull toward compulsive redosing, with agitation, high blood pressure and psychosis-like states at the top end. Serious adverse events and deaths are on record. Not something to treat like ketamine.
Resources
This entry is here for reference.
Research
- 2017first citedTwo Cases of Non-fatal Intoxication with a Novel Street Hallucinogen: 3-Methoxy-Phencyclidine.
- 2026most recentADME profile of phencyclidine (PCP) analogues: emerging dissociative hallucinogens 3-MeO-PCP (C…
- 1.3-Methoxy-Phencyclidine Induced Psychotic Disorder: A Literature Review and an (18)F-FDG PET/CT Case Report.
- 2.Intoxication with 3-MeO-PCP alone: A case report and literature review
- 3.ADME profile of phencyclidine (PCP) analogues: emerging dissociative hallucinogens 3-MeO-PCP (CAS: 72242-03-6) and 4-MeO-PCP (CAS: 2201-35-6)-a multi-in silico approach for comprehensive prediction of absorption, distribution, metabolism and excretion relevant to clinical and forensic toxicology.
- 4.Qualitative and quantitative in silico toxicity profiling of "angel dust": phencyclidine (PCP) analogues as new psychoactive substances (3-HO-PCP, 3-MeO-PCP, 4-MeO-PCP, 3-HO-PCE, 3-MeO-PCE, 4-MeO-PCE).
- 5.Qualitative confirmation of 30 phencyclidine analogs in human blood and urine using GC-HRMS and a self-built library search.
- 6.4-MeO-PCP and 3-MeO-PCMo, new dissociative drugs, produce rewarding and reinforcing effects through activation of mesolimbic dopamine pathway and alteration of accumbal CREB, deltaFosB, and BDNF levels.
- 7.Newly Emerging Drugs of Abuse.
- 8.Detectability of Dissociative Psychoactive Substances in Urine by Five Commercial Phencyclidine Immunoassays.
- 9.Metabolites to parent 3-MeO-PCP ratio in human urine collected in two fatal cases.
- 10.The First Fatal Intoxication with 3-MeO-PCP in the UK and a Review of the Literature.
- 11.Two Fatal Intoxications Involving 3-Methoxyphencyclidine.
- 12.A non-fatal intoxication and seven deaths involving the dissociative drug 3-MeO-PCP.
15 listed here; entry last updated August 2026
Reviews
My notesprivate to this device
FAQ
How is it different from ketamine?
It is more stimulating, longer, more dopamine-active, and has a narrower margin, so it is less forgiving.
What is the main danger?
Overshooting is easy because onset is slow; higher exposure risks agitation, blood-pressure spikes, and psychosis-like states.
What to avoid it with?
Other depressants (sedation and breathing) and stimulants (cardiac and psychological strain).
Adverse effects
- Narrow margin; easy to overshoot
- Agitation, high blood pressure, mania-like or psychotic states
- Strong potential for compulsive redosing