3-MeO-PCPr
3-MeO-PCPr is a dissociative research chemical of the arylcyclohexylamine class.citation needed It is the N-propyl homologue of 3-MeO-PCE and is reported to be slightly less potent than PCP while producing a somewhat less manic experience by comparison. As a relatively obscure research chemical, very limited data exists regarding its safety profile, pharmacology, and long-term effects. Like other arylcyclohexylamines, it may carry a risk of habit formation.1
Dosage & Duration
Dosage
Doses are population estimates that vary widely between individuals.
Duration
Subjective Effects
Legacy content. A statistically backed ontology from Mindstate Design Labs is coming soon.
Available documentation of 3-MeO-PCPr is minimal and consists mainly of comparative characterization rather than detailed accounts of the experience. It is described as somewhat less potent than PCP, and as producing a less manic quality than related compounds.
See also: Dissociative Intensity Scale, Subjective Effects of Dissociatives
Pharmacology
Pharmacodynamics
Published literature places 3-MeO-PCPr among arylcyclohexylamines perceived as ketamine-like dissociatives and believed to act predominantly through NMDA-receptor antagonism. The compound-specific study was analytical, not a clinical pharmacology study, so this is not a complete receptor profile or evidence of human efficacy. [S1][S2]2
Pharmacokinetics
The inspected analytical paper and PCP-NPS review reported no compound-specific absorption, bioavailability, distribution, metabolism, elimination, or half-life values for 3-MeO-PCPr; numerical pharmacokinetic fields should remain empty. [S1][S2]citation needed
Interactions
An unlisted combination is an unknown one, not a safe one. Check a dedicated combination chart before mixing.
Tolerance
Tolerance timelines are rules of thumb, not exact schedules, and vary widely between individuals and use patterns.
Dissociatives (NMDA receptor antagonists)
Harm Potential
Addiction & Dependence
Psychological
ModerateClassified as habit-forming, though specific addiction potential has not been formally characterized.
History & Culture
Online documentation
A surviving Bluelight thread dated 2 October 2011 contains a self-report and discussion of 3-MeO-PCPr. This establishes online discussion by that date, not first synthesis or first use.3
Legality
International
As of 23 August 2026, 3-MeO-PCPr (N-propyl-1-(3-methoxyphenyl)cyclohexan-1-amine) is not named or chemically designated in the current complete INCB Yellow, Green or Red Lists. The Green List instead places PCE (N-ethyl-1-phenylcyclohexylamine) and PHP/PCPy (1-(1-phenylcyclohexyl)pyrrolidine) in Schedule I and separately places 3-methoxyphencyclidine (1-(1-(3-methoxyphenyl)cyclohexyl)piperidine) in Schedule II. Those exact designations do not cover the target, which the analytical literature identifies as the 3-methoxyphenyl N-propyl compound rather than the N-ethyl, pyrrolidine or piperidine compounds. The Green List extends control to salts and applicable stereoisomers of listed substances, not to otherwise distinct N-alkyl analogues. INCB's March 2026 notice adds only MDMB-FUBINACA to Schedule II, with effect from 25 November 2026, and does not name 3-MeO-PCPr. The current INCB materials therefore establish no scheduling of 3-MeO-PCPr under the 1961, 1971 or 1988 Conventions.
By Country
References
Source Pages
Citations
Further Reading
Article Status
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