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    DMHA molecular structure

    DMHA Stats & Data

    Amidrine Vaporpac Octodrine 2-aminoisoheptane 1,5-dimethylhexylamine
    NPS DataHub
    MW129.25
    FormulaC8H19N
    CAS543-82-8
    IUPAC6-methylheptan-2-amine
    SMILESCC(C)CCCC(C)N
    InChIKeyQNIVIMYXGGFTAK-UHFFFAOYSA-N
    Psychoactive Class Stimulant
    Half-Life Unknown in humans; no authoritative half-life reported.

    Effect Profile

    Curated
    Stimulant 5.6

    Strong focus and anxiety/jitters with mild stimulation and euphoria

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

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Unknown in humans; no authoritative half-life reported.
    Addiction Potential
    Moderate psychological dependence risk typical of stimulants; compulsive redosing and tolerance can develop with frequent use.

    Tolerance Decay

    Full tolerance 14d Half tolerance 3d Baseline ~7d

    Estimates reflect stimulant-class tolerance patterns inferred from user reports; high uncertainty.

    Cross-Tolerances

    DMAA
    60% ●○○
    Caffeine
    20% ●○○

    Harm Reduction

    drugs.wiki

    Human pharmacokinetic data (including half-life) are not published in authoritative databases, so apparent 4–6 h duration is based on user reports rather than measured plasma kinetics. Pre‑workout and ‘energy’ products that list DMHA/Octodrine often include additional stimulants (e.g., caffeine, synephrine, higenamine, yohimbine), which can significantly increase heart rate, blood pressure, and adverse-event risk; single-ingredient use reduces uncertainty from proprietary blends. The hydrochloride vs freebase salt, product purity, and inaccurate labels can change potency by tens of percent; start low, go slow, and avoid redosing until well past the onset window. As a sympathomimetic, DMHA may worsen hypertension, arrhythmias, anxiety, and insomnia; avoid if you have cardiovascular disease, uncontrolled thyroid disease, or panic disorder, and do not use late in the day. Mixing with MAOIs can precipitate hypertensive crises; stacking with other stimulants (including ‘fat burners’) increases risks of tachycardia, hyperthermia, and vasoconstriction—particularly during strenuous exercise. Alcohol can mask intoxication from stimulants and add strain on the heart; if used, avoid combining and ensure cooling, hydration, and rest during workouts. Intranasal use can cause pronounced nasal irritation and local vasoconstriction; oral routes are generally lower-risk. Tolerance to stimulant effects builds rapidly with frequent use; spacing use (days to weeks) lowers crash/insomnia and reduces escalation. Legal/regulatory note: the U.S. FDA considers supplements containing DMHA to be adulterated; products may be seized or reformulated without notice, adding supply variability and labeling uncertainty.

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