3-MeO-PCPy
3-MeO-PCPy is a dissociative research chemical and the 3-methoxy analogue of rolicyclidine (PCPy).1 Structurally related to phencyclidine (PCP), it is reported to produce less pronounced opioid-like effects than PCP, though such effects remain notable. Very limited information is available regarding its pharmacology, toxicity, or safe dosage ranges. It is considered habit-forming, and extreme caution is advised due to the scarcity of available data.
Dosage & Duration
Dosage
Doses are population estimates that vary widely between individuals.
Duration
Subjective Effects
Pharmacology
Pharmacodynamics
3-MeO-PCPy is the 3-methoxy analogue of rolicyclidine (PCPy).2 It reportedly exhibits opioid-like activity that is less pronounced than that of phencyclidine (PCP) but still notable. Detailed receptor-level characterization remains limited.
Pharmacokinetics
A study using rat urine and pooled human liver microsomes identified 3-MeO-PCPy pathways including aliphatic hydroxylation of the cyclohexyl and pyrrolidine rings, aromatic hydroxylation, carboxylation after ring opening, O-demethylation, and glucuronidation.1 In expressed-enzyme incubations, CYP2B6 catalyzed aliphatic hydroxylation, while CYP2C9 and CYP2D6 catalyzed O-demethylation.1 The detailed in-vivo metabolite profile came from rats, and the human findings were produced in vitro; clinical data are needed before inferring human pharmacokinetic variability or whole-body parameters.1
Interactions
An unlisted combination is an unknown one, not a safe one. Check a dedicated combination chart before mixing.
Tolerance
Harm Potential
Addiction & Dependence
Psychological
Classified as habit-forming by community harm reduction resources, suggesting some potential for compulsive use patterns.
History & Culture
3-MeO-PCPy is a 3-methoxy analogue of rolicyclidine (PCPy),2 belonging to the arylcyclohexylamine class of dissociative compounds. It represents one of several structural modifications explored within this chemical class, which also includes the related compound phencyclidine (PCP).2 Detailed documentation regarding its specific synthesis history, original development, and cultural significance remains limited in available literature.
Legality
International
As of 23 August 2026, 3-MeO-PCPy (3-methoxyrolicyclidine) is not named or chemically designated in the current complete INCB Yellow, Green or Red Lists. The Green List instead places unmodified rolicyclidine (PHP/PCPy; 1-(1-phenylcyclohexyl)pyrrolidine) in Schedule I and separately places 3-methoxyphencyclidine (1-(1-(3-methoxyphenyl)cyclohexyl)piperidine) in Schedule II. Those entries do not cover the target: the former lacks the 3-methoxy substitution and the latter has a piperidine ring rather than PCPy's pyrrolidine ring. INCB's March 2026 notice adds only MDMB-FUBINACA to Schedule II, with effect from 25 November 2026, and does not name 3-MeO-PCPy. Accordingly, the current INCB materials establish no scheduling of 3-MeO-PCPy under the 1961, 1971 or 1988 conventions.
By Country
References
Citations
- Julian A. Michely, Sascha K. Manier, Achim T. Caspar, Simon D. Brandt, Jason Wallach, & Hans H. Maurer. (2017). New Psychoactive Substances 3-Methoxyphencyclidine (3-MeO-PCP) and 3-Methoxyrolicyclidine (3-MeO-PCPy): Metabolic Fate Elucidated with Rat Urine and Human Liver Preparations and their Detectability in Urine by GC-MS, LC-(High Resolution)-MSn and LC-(High Resolution)-MS/MS. 15(5), 692-712. https://doi.org/10.2174/1570159x146661610181517161234
- Michely, J.A., Manier, S.K., Caspar, A.T., Brandt, S.D., Wallach, J., & Maurer, H.H.. (2017). New Psychoactive Substances 3-Methoxyphencyclidine (3-MeO-PCP) and 3-Methoxyrolicyclidine (3-MeO-PCPy): Metabolic Fate Elucidated with Rat Urine and Human Liver Preparations and their Detectability in Urine by GC-MS, LC-(High Resolution)-MSn and LC-(High Resolution)-MS/MS. pmc.ncbi.nlm.nih.gov, 15(5), 692–718. https://doi.org/10.2174/1570159x1466616103111373112345
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- N.J. Stat. Ann. § 2C:35-2, as set out in P.L. 2012, c. 17, § 2. pub.njleg.state.nj.us (n.d.). https://pub.njleg.state.nj.us/Bills/2012/PL12/17_.HTM1
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- N.Y. Public Health Law §§ 3302(4) and 3306. nysenate.gov (n.d.). https://www.nysenate.gov/legislation/laws/PBH/33021
- N.Y. Public Health Law §§ 3302(4) and 3306. nysenate.gov (n.d.). https://www.nysenate.gov/legislation/laws/PBH/33061
- N.D. Cent. Code §§ 19-03.1-01(7) and 19-03.1-23(7). ndlegis.gov (n.d.). https://ndlegis.gov/cencode/t19c03-1.pdf1
- 6 CMC §§ 2102(c), 2111(c), 2114(c). cnmilaw.org (n.d.). https://cnmilaw.org/pdf/cmc_section/T6/2102.pdf1
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- Or. Rev. Stat. §§ 475.005(6), 475.752 and 475.908; Or. Admin. R. 855-080-0021. oregonlegislature.gov (n.d.). https://www.oregonlegislature.gov/bills_laws/ors/ors475.html1
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- Tex. Health & Safety Code §§ 481.002(6), 481.106. tcss.legis.texas.gov (n.d.). https://tcss.legis.texas.gov/resources/hs/pdf/hs.481.pdf1
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