The synthesis of 4-MeO-PCP was first reported in 1965 by the Parke-Davis medicinal chemist Victor Maddox. A 1999 review published by a chemist using the pseudonym John Q. Beagle suggested the potency of 4-MeO-PCP in man was reduced relative to PCP. Two years later, Beagle published a detailed description of the synthesis and qualitative effects of 4-MeO-PCP which he said possessed 70% of the potency of PCP.
|Common names||4-MeO-PCP, Methoxydine|
Chemical Properties of 4-MeO-PCP
4-MeO-PCP, or 4-Methoxyphencyclidine, is a synthetic dissociative of the arylcyclohexylamine class. 4-MeO-PCP contains cyclohexane, a six member saturated ring, bonded to two additional rings at R1. One of these rings is a piperidine ring (a nitrogenous six member ring) bonded at its nitrogen group. The other ring is an aromatic phenyl ring substituted at R4 with a methoxy group. 4-MeO-PCP is a PCP derivative, and structurally analogous to 3-MeO-PCP.
Disclaimer: The effects listed below cite the Subjective Effect Index (SEI), an open research literature based on anecdotal user reports and the personal analyses of Psychonaut contributors. As a result, they should be viewed with a healthy degree of skepticism.
- Motor control loss
- Perception of bodily lightness
- Physical autonomy
- Physical euphoria
- Spatial disorientation
- Spontaneous physical sensations
- Tactile disconnection
- Tactile suppression
- Optical sliding
- Visual disconnection
- Visual acuity suppression
- Double vision
- Pattern recognition suppression
- Frame rate suppression
- Perspective distortions
- Environmental cubism
- Environmental orbism
- Scenery slicing
- Anxiety suppression
- Consciousness disconnection
- Compulsive redosing
- Conceptual thinking
- Creativity enhancement
- Déjà vu
- Dream potentiation
- Existential self-realization
- Memory suppression
- Ego death
- Immersion enhancement
- Increased music appreciation
- Analysis suppression
Potentially dangerous interactions
- Legal status
- United Kingdom
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