Home
    Disclaimer
    Fenethylline molecular structure

    Fenethylline Stats & Data

    Fitton Captagon Biocapton Amfetyline Phenethylline
    NPS DataHub
    MW377.87
    FormulaC18H24ClN5O2
    CAS1892-80-4
    IUPAC1,3-dimethyl-7-[2-(1-phenylpropan-2-ylamino)ethyl]purine-2,6-dione;hydrochloride1,3-dimethyl-7-[2-(1-phenylpropan-2-ylamino)ethyl]purine-2,6-dione;hydron;chloride
    SMILES[Cl-].CC(NCCn1cnc2n(C)c(=O)n(C)c(=O)c12)Cc1ccccc1.[H+]
    InChIKeyMVXGSLGVWBVZCA-UHFFFAOYSA-N
    Phenethylamines; 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 Parent codrug: rapid cleavage (short t½, not the primary driver of effect); active metabolite theophylline ~4–8 h; amphetamine metabolite elimination varies with urinary pH and typically spans many hours.

    Pharmacology

    DrugBank
    State Solid

    Receptor Profile

    Receptor Actions

    Agonists
    Amphetamine: TAAR1 agonist
    Antagonists
    Theophylline: Adenosine receptor antagonist (A2aR)
    Other
    Prodrug metabolizing to amphetamine (24.5% of oral dose) and theophylline (13.7% of oral dose)
    Dopamine-norepinephrine-serotonin releasing agent (SNDRA)

    Effect Profile

    Curated
    Stimulant 6.9

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

    Stimulation / Energy×3
    7
    Euphoria / Mood Lift×2
    5
    Focus / Productivity×2
    10
    Anxiety / Jitters×1
    6

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Parent codrug: rapid cleavage (short t½, not the primary driver of effect); active metabolite theophylline ~4–8 h; amphetamine metabolite elimination varies with urinary pH and typically spans many hours.
    Addiction Potential
    Moderate-to-high, broadly comparable to other amphetamine-type stimulants; the codrug’s theophylline fraction may alter the subjective profile but does not eliminate stimulant misuse liability.

    Cross-Tolerances

    Amphetamine
    70% ●○○
    Methamphetamine
    60% ●○○
    Cathinones
    50% ●○○
    Other phenethylamine stimulants
    40% ●○○

    Legal Status

    Controlled internationally under the UN Convention on Psychotropic Substances 1971.
    Country Status Notes
    Australia Fenethylline is a Schedule 9 prohibited substance.
    Brazil Fenethylline is a Class A3 psychoactive substance.
    Canada Fenethylline is a Schedule III drug in Canada.
    Germany Fenethylline is a Anlage III(Schedule III) drug under the Betäubungsmittelgesetz(controlled substances law of Germany) and can only be obtained by prescription.
    United Kingdom Fenethylline is a Class C drug in the United Kingdom.
    United States Fenethylline is a Schedule I controlled substance in the United States.

    Harm Reduction

    drugs.wiki

    Reasoning for key harm-reduction updates: 1) Modern “Captagon” tablets are almost universally amphetamine-based counterfeits, not fenethylline. Multiple EMCDDA/EUDA reports show EU-seized tablets typically contain amphetamine (often with caffeine) and no fenethylline; some analyses estimate ≈32 mg amphetamine sulfate per tablet. This means dose/effect expectations for genuine fenethylline do not apply to street tablets; accurate identification requires instrumental analysis (e.g., GC/MS or LC-MS). 2) Fenethylline is a codrug cleaved to amphetamine and theophylline in vivo; the methylxanthine fraction contributes adenosine antagonism and PDE inhibition, raising heart rate and excitability and—at higher exposures—seizure risk. Thus, avoiding extra caffeine and being alert to theophylline-like toxicity (nausea, tremor, tachyarrhythmia) is prudent. 3) Stimulants combined with MAOIs can precipitate hypertensive crisis; standard references list amphetamine as contraindicated within 14 days of MAOI therapy. Treat fenethylline with the same caution because its active stimulant metabolite is amphetamine. 4) Mixing with serotonergic antidepressants and CYP2D6 inhibitors increases serotonin-syndrome risk for amphetamine; monitor closely or avoid. 5) Theophylline is metabolized mainly by CYP1A2; inhibitors can raise levels and toxicity. This underpins caution with drugs that inhibit CYP1A2 and with heavy caffeine co-use. 6) Urinary pH strongly modulates amphetamine elimination; alkalinization prolongs effects/toxicity, while acidification increases clearance. Users should avoid deliberate alkalinization when concerned about over-stimulation. 7) Environment/heat: stimulants elevate body temperature; hot indoor/outdoor settings increase the risk of hyperthermia and organ damage—plan cooling breaks and hydration with electrolytes. 8) General stimulant harm reduction advises avoiding polystimulant stacks and using test services where possible; EUDA notes that reagents are insufficient to verify fenethylline—instrumental drug checking is needed. 9) Cardiovascular screening: amphetamine-class agents are contraindicated in significant cardiovascular disease/hyperthyroidism/glaucoma; treat fenethylline similarly due to its active amphetamine metabolite and theophylline side-effects. 10) Legal status: fenethylline is internationally controlled (e.g., US Schedule I; UN Psychotropics Schedule II); possession/supply penalties may be severe.

    References

    ← Back to Fenethylline