3-MeO-PCPr
Aliases: 3-methoxyphencyclidine propylamino
Summary
3-MeO-PCPr is a potent N-propyl analogue of 3-MeO-PCP with high NMDA receptor affinity (Ki = 25 nM). It is notably more stimulating and euphoric than many related dissociatives due to pronounced dopamine reuptake inhibition, which significantly increases compulsive redosing risk. Individual sensitivity varies widely.
Dose Information
| ROA | Light | Common | Strong | Heavy |
|---|---|---|---|---|
| Oral | 5-8mg | 8-15mg | 15-20mg | 20mg+ |
| Insufflated | 1-3mg | 3-8mg | 8-15mg | 15mg+ |
Onset, Duration & After-effects
| ROA | Onset | Comeup | Peak | Offset |
|---|---|---|---|---|
| Oral | 15-30 min | 30-60 min | 2-4 hrs | 2-4 hrs |
| Insufflated | 5-10 min | 15-30 min | 1-3 hrs | 2-3 hrs |
Effect Profile
Scores (1–10) curated from multiple sources:
- Effect keyword matching from PsychonautWiki catalog
- Weighted by importance: core (×3), major (×2), minor (×1)
Strong mania, motor impairment, and dissociative depth
Moderate euphoria with low stimulation and anxiety/jitters
Tolerance
Tolerance Decay
Estimates reflect community experience with arylcyclohexylamines (rapid tolerance build with partial reversal over 1β4 weeks) and should be treated as approximate. Crossβtolerance across NMDA antagonists is expected but extent varies.
Cross-Tolerances
Effects
- Stimulation
- Physical euphoria
- Analgesia
- Pain relief
- Increased heart rate
- Numbness
- Loss of balance
- Nausea
- Physical disconnection
- Sedation
- Cognitive euphoria
- Motor control loss
- Compulsive redosing
- Mania
- Delusion
- Confusion
- Amnesia
- Depersonalization
- Dissociation
- Time distortion
- Tactile enhancement
- Increased music appreciation
- Disinhibition
- Tactile suppression
- Light sensitivity
- Spatial disorientation
- Double vision
- Pattern recognition suppression
- Visual disconnection
- Auditory distortion