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    5-BPDi molecular structure

    5-BPDi Stats & Data

    Indanyl-α-php 3',4'-trimethylene-α-pyrrolidinohexanophenone
    NPS DataHub
    MW285.43
    FormulaC19H27NO
    CAS2748304-64-3
    IUPAC1-(2,3-dihydro-1H-inden-5-yl)-2-pyrrolidin-1-ylhexan-1-one
    SMILESCCCCC(N1CCCC1)C(=O)c1ccc2CCCc2c1
    InChIKeyWETQQOQCDBNIKE-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 Cathinone
    Psychoactive Class Stimulant
    Half-Life Not formally studied; by analogy to α-PHP/MDPV, effects may persist despite falling plasma levels; repeated dosing extends duration.

    Effect Profile

    Curated
    Stimulant 5.9

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

    Stimulation / Energy×3
    7
    Euphoria / Mood Lift×2
    6
    Focus / Productivity×2
    7
    Anxiety / Jitters×1
    10

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Not formally studied; by analogy to α-PHP/MDPV, effects may persist despite falling plasma levels; repeated dosing extends duration.
    Addiction Potential
    Moderate to high. As with other pyrrolidinophenone cathinones (e.g., α-PVP, MDPV), compulsive redosing and multi-hour binges are commonly reported; withdrawal dysphoria, insomnia, and anxiety can follow cessation.

    Tolerance Decay

    Full tolerance 2d Half tolerance 7d Baseline ~21d

    Acute tolerance within a session is common (diminishing euphoria with repeated lines) alongside increasing side effects. Subjective tolerance decays over 2–4 weeks in many users. Data quality is low; values are inferred from patterns seen with α-PVP/MDPV and community reports.

    Cross-Tolerances

    Other synthetic cathinones (esp. pyrrolidinophenones)
    70% ●○○
    Amphetamine / cocaine (classical stimulants)
    40% ●○○

    Harm Reduction

    drugs.wiki

    5-BPDi (Indanyl-α-PHP) is a hexanone pyrrolidinophenone first detected on the grey market circa mid-2010s; formal human pharmacology/toxicology is lacking. As with related pyrrolidinophenones (α-PVP/MDPV), strong dopaminergic/noradrenergic stimulation can cause marked tachycardia, hypertension, anxiety, bruxism, vasoconstriction (cold/numb extremities), and hypervigilance; plan a dose cap, avoid heat/exertion, and monitor pulse/BP if possible. Residual stimulation often outlasts euphoria—late redosing commonly leads to insomnia and paranoia; set a hard stop time and prepare sleep hygiene or non-alcoholic sedating measures (without mixing high doses of depressants). Avoid combining with other stimulants or MAOIs due to hypertensive crisis/arrhythmia risk; tramadol and bupropion increase seizure risk; decongestants increase vasoconstriction. Because cathinone powders are frequently mis-sold/adulterated, use lab drug checking where available or multiple reagents (Marquis, Froehde, Simon’s, Zimmermann, Morris) and start with a 0.5–1 mg allergy test; expect that names/labels may not match contents. Oral administration is safer than insufflation; if snorting, reduce tissue damage and infection risk by using sterile personal equipment, crushing finely, rinsing with sterile saline, and spacing lines. Maintain hydration with electrolytes (about 250 mL/h at rest up to ~500 mL/h if active) without overhydrating; eat before use and plan a recovery window with sleep. Avoid use if you have cardiovascular disease, severe anxiety/psychosis risk, or during pregnancy/breastfeeding. Seek urgent care for chest pain, severe headache, confusion, hyperthermia, seizures, or prolonged psychosis—these can reflect stimulant toxicity or excited delirium.

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