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A-PHP
A-PHP is a synthetic stimulant in the substituted cathinone and pyrrolidine classes1. First synthesized in the 1960s, it later emerged as a replacement for α-PVP. Its longer alkyl side chain distinguishes it from α-PVP, adding one carbon.2 Rodent studies indicate abuse potential for pyrrolidino-cathinones, with α-PHP appearing to have the greatest addictive liability among the synthetic cathinones tested, although information is insufficient for firm conclusions1.
Dosage & Duration
Dosage
Doses are population estimates that vary widely between individuals.
Duration
Subjective Effects
Pharmacology
Pharmacodynamics
The mechanism of action of α-PHP has not been established. In radioligand binding and functional assays, α-PHP was found to inhibit uptake at DAT, NET and SERT, with uptake-inhibition potency ranked DAT > NET >> SERT2, partially blocking transporter proteins and increasing these monoamines in the brain, but this remains an inference because substantial pharmacological research is lacking.
Pharmacokinetics
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.
Dopaminergic stimulants
Harm Potential
Addiction & Dependence
Psychological
Extremely HighChronic use is regarded as highly addictive, with substantial abuse potential and a capacity to cause psychological dependence. A-PHP is especially associated with compulsive redosing, where users may find it extremely difficult to stop taking more even after psychotic symptoms appear. Abruptly stopping after sustained use may be followed by cravings and withdrawal symptoms.
Toxicity
Because its rush can be very powerful, α-PHP may produce uncomfortable or painful cardiac sensations, particularly with abuse or prolonged use; sudden spikes of blood pressure may manifest as an extremely uncomfortable sensation, particularly when vaporized or injected.
Psychosis Risk
Can result in stimulant psychosis presenting with paranoia, hallucinations, or delusions, particularly when dosed too highly or frequently. A review of treatment for similar stimulant-induced psychosis reports that approximately 5-15% of users do not fully recover. Psychotic and schizophrenic symptoms may occur even before users stop redosing, and delusional states are commonly reported when the substance is abused.
Seizure Risk
Misuse may make seizures more likely in some individuals by reducing the seizure threshold.
History & Culture
Legality
International
UN Convention on Psychotropic Substances Schedule II (added March 2020)
By Country
References
Source Pages
Citations
Further Reading
Article Status
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