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    4-Methoxybutyrfentanyl molecular structure

    4-Methoxybutyrfentanyl Stats & Data

    4-meo-bf 4-meo-butryfentanyl 4-MeO-Butyrfentanyl
    NPS DataHub
    MW380.53
    FormulaC24H32N2O2
    CAS2088842-68-4
    IUPACN-(4-methoxyphenyl)-N-[1-(2-phenylethyl)piperidin-4-yl]butanamide
    SMILESCCCC(=O)N(C1CCN(CCc2ccccc2)CC1)c1ccc(OC)cc1
    InChIKeyFNVSEQCPMXWQKG-UHFFFAOYSA-N
    Phenethylamines; Opioids; 2020/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2021/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2022/1. Von 2-Phenethylamin abgeleitete Verbindungen
    Chemical Class Opioid
    Psychoactive Class Depressant
    Half-Life Not formally studied; likely short-acting kinetics similar to butyrylfentanyl analogues (rapid distribution minutes; elimination on the order of hours).

    History & Culture

    4-MeO-Butyrfentanyl is a rare synthetic opioid belonging to the fentanyl analogue class of compounds. The substance has received minimal documentation in both scientific literature and online harm reduction communities, and its precise history of synthesis and development remains poorly documented. It should be distinguished from the related compound butyrfentanyl, which has been more extensively characterized.

    Effect Profile

    Curated
    Opioid 7.6

    Strong euphoria and pain relief with moderate itching/nausea, low sedation

    Euphoria / Warmth×3
    10
    Analgesia×2
    8
    Sedation / Relaxation×1
    3
    Itching / Nausea×1
    6

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Not formally studied; likely short-acting kinetics similar to butyrylfentanyl analogues (rapid distribution minutes; elimination on the order of hours).
    Addiction Potential
    High. Rapid tolerance and physical dependence develop similarly to fentanyl. Severe withdrawal can begin within 8–12 h of cessation after sustained use.

    Tolerance Decay

    Full tolerance 3d Half tolerance 14d Baseline ~28d

    Opioid tolerance builds rapidly with daily/frequent exposure and decays over weeks; risk of overdose is highest after abstinence due to loss of tolerance. Data specific to 4‑MeO‑BF are sparse; estimates extrapolated from fentanyl-class opioids.

    Cross-Tolerances

    all µ‑opioid agonists (fentanyl, morphine, oxycodone, heroin, etc.)
    70% ●○○

    Harm Reduction

    drugs.wiki

    4-MeO-BF is a highly potent ‘research’ fentanyl-type opioid first identified in Europe in 2015. Clinically confirmed intoxications have shown life-threatening opioid toxicity at low ng/mL serum levels, consistent with fentanyl-class potency. Purity and composition of unregulated opioid products vary widely, and mixtures with multiple high‑potency opioids or sedatives are increasingly common; use volumetric dosing, avoid redosing quickly, and never eyeball. Metered nasal sprays or precisely diluted oral solutions (e.g., ≤1 mg/mL) with 0.01 mL syringes can reduce dosing error. Naloxone reverses toxicity but has shorter action than many opioids; repeated doses or continuous infusion and cardiorespiratory monitoring are often required; re‑narcotisation within 20–60 min is well described. Combining with benzodiazepines, alcohol, GHB/GBL, barbiturates, pregabalin/gabapentin, or sedating antipsychotics markedly increases respiratory depression risk. Opioid + stimulant (“speedball”) may mask sedation while respiratory depression progresses—avoid. Serotonin toxicity has been reported with fentanyl combined with SSRIs/SNRIs or MAO‑Is; use extra caution if on serotonergic medicines. Accidental occupational exposure to powders/aerosols of fentanyl analogues is a recognised risk for labs and responders; wear appropriate PPE and have naloxone available when handling bulk material. Because duration is short, frequent redosing is a major driver of overdose—plan set/setting, avoid using alone, carry naloxone, and prioritise oxygen/ventilation in emergencies.

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