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    a-PHP Stats & Data

    Pv-7 aphp α-php αphp alpha-php
    NPS DataHub
    MW245.36
    FormulaC16H23NO
    CAS13415-86-6
    IUPAC1-phenyl-2-pyrrolidin-1-ylhexan-1-one
    SMILESCCCCC(N1CCCC1)C(=O)c1ccccc1
    InChIKeyKYIJLDDXQWBNGX-UHFFFAOYSA-N
    Phenethylamines; Cathinones; 2020/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2021/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2022/1. Von 2-Phenethylamin abgeleitete Verbindungen
    Chemical Class Amphetamine
    Psychoactive Class Stimulant
    Half-Life Unknown in humans; effects suggest several hours with long after-effects, similar to related pyrrolidinyl cathinones.

    Effect Profile

    Curated + 10 Reports
    Stimulant 6.4

    Strong anxiety/jitters, euphoria, and focus with mild stimulation

    Stimulation / Energy×3
    5
    Euphoria / Mood Lift×2
    9
    Focus / Productivity×2
    9
    Anxiety / Jitters×1
    10

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Unknown in humans; effects suggest several hours with long after-effects, similar to related pyrrolidinyl cathinones.
    Addiction Potential
    High. Noted for strong craving and compulsive redosing, especially with vaporizing/insufflation; significant risk of psychological dependence.

    Tolerance Decay

    Full tolerance 2d Half tolerance 7d Baseline ~14d

    Rapid escalation in a single session is common due to short duration and fiendishness, particularly when vaporized. Several days to weeks of abstinence are typically needed to approach baseline sensitivity. Data quality primarily anecdotal.

    Cross-Tolerances

    Other pyrrolidinyl cathinones (e.g., α‑PVP, α‑PiHP, MDPV)
    60% ●○○

    Experience Report Analysis

    Erowid
    10 Reports
    2014–2021 Date Range
    8 With Age Data
    6 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid

    Effects aggregated from 10 experience reports (10 Erowid)

    10 Reports
    6 Effects Detected
    3 Positive
    3 Adverse
    0 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 3

    Euphoria 70.0% 70%
    Focus Enhancement 70.0% 70%
    Stimulation 50.0% 70%

    Adverse Effects 3

    Anxiety 80.0% 70%
    Increased Heart Rate 40.0% 70%
    Nausea 30.0% 70%

    Real-World Dose Distribution

    62K Doses

    From 23 individual dose entries

    Rectal (n=5)

    Median: 25.0mg 25th: 25.0mg 75th: 25.0mg 90th: 25.0mg

    Insufflated (n=8)

    Median: 25.0mg 25th: 6.75mg 75th: 50.0mg 90th: 54.5mg
    mg/kg median: 0.382 mg/kg 75th: 0.689

    Form / Preparation

    Most common forms and preparations reported

    Harm Reduction

    drugs.wiki

    - Potency is high and variable; begin with an allergy test (≤1 mg) and titrate cautiously. User reports and The Drug Users Bible indicate very fast onset and meaningful effects from single-digit milligram doses. Batch-to-batch variability is common in the NPS market.

    - Vaporizing and insufflation produce rapid spikes that strongly reinforce compulsive redosing (“fiending”), increasing cardiovascular strain, sleep loss, and psychosis risk; many users describe vaping as particularly moreish. Avoid marathon sessions; plan hard stops and sleep recovery.

    - Intranasal use is described as caustic/irritating; some users report significant nasal damage and bleeding lasting days. Consider oral routes to reduce local harm, though systemic risks remain. Rinse nasal passages with saline post-use if insufflating.

    - Psychosis, paranoia, and severe anxiety are commonly reported during binges or after prolonged sleep deprivation. Strictly limit session length, ensure sleep, and avoid redosing when anxiety or tachycardia rise.

    - Cardiovascular risks include tachycardia, hypertension, chest pain, and vasoconstriction; avoid if you have heart disease, arrhythmias, uncontrolled hypertension, or are on interacting meds. Seek medical care for persistent chest pain, severe headache, or confusion.

    - Maintain hydration and electrolytes; avoid overheating. Stimulants can suppress appetite—plan nutrition, limit caffeine.

    - Avoid combining with MAOIs or other potent stimulants due to hypertensive and hyperadrenergic crises. Be cautious with tramadol or bupropion (lowered seizure threshold) and with serotonergic meds (agitation/overstimulation).

    - Reagent test and, where possible, use lab drug-checking; cathinone markets are adulterated and mislabeling among pyrovalerone analogues is common.

    - Tolerance builds quickly during repeated use and fades over days to weeks; frequent redosing escalates total intake rapidly. Space sessions by at least 1–2 weeks to reduce compulsive patterns.

    - Using benzodiazepines or alcohol to ‘come down’ can mask warning signs and add respiratory risk if combined; if used, keep doses minimal, avoid alcohol/opioids, and prioritize sleep hygiene.

    - Avoid IV use; it greatly increases acute harms and addiction liability and is not supported by harm-reduction communities for this class.

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