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    ADB-PINACA isomer 1 Stats & Data

    NPS DataHub
    MW344.46
    FormulaC19H28N4O2
    IUPACN-(1-amino-2,3-dimethyl-1-oxobutan-2-yl)-1-pentylindazole-3-carboxamide
    SMILESCCCCCn1nc(C(=O)NC(C)(C(C)C)C(N)=O)c2ccccc12
    InChIKeyWLFSZTSBEOZUTQ-UHFFFAOYSA-N
    Cannabinoids; 2020/2.1 Von Indol Pyrazol und 4-Chinolon abgeleitete Verbindungen; 2021/2.1 Von Indol Pyrazol und 4-Chinolon abgeleitete Verbindungen; 2022/2.1 Von Indol Pyrazol und 4-Chinolon abgeleitete Verbindungen
    Chemical Class Cannabinoid
    Half-Life Parent compound ~2–4 h; major hydroxylated/de-adamantyl metabolites 4–8 h (longer in chronic users).

    Tolerance & Pharmacokinetics

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    Half-Life
    Parent compound ~2–4 h; major hydroxylated/de-adamantyl metabolites 4–8 h (longer in chronic users).
    Addiction Potential
    High. Daily use with rapid escalation and pronounced withdrawal (irritability, insomnia, sweats, nausea) is frequently reported. Comparable to other potent SCRAs, and higher than phytocannabinoid (THC) preparations.

    Tolerance Decay

    Full tolerance 5d Half tolerance 10d Baseline ~28d

    Frequent SCRA administration leads to rapid tolerance build-up and withdrawal (irritability, insomnia, sweats, nausea) described widely in community reports. Decay appears partial over 1–2 weeks with further recovery by ~4 weeks in many users; exact kinetics are not established.

    Cross-Tolerances

    Other synthetic cannabinoids (indazole/indole carboxamides)
    60% ●○○
    Δ9-THC (cannabis)
    30% ●○○

    Harm Reduction

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    • Identification/labels: “Spice/K2” products and vendor labels (including “isomer 1”) are unreliable; contents and dose per gram vary widely, so treat any sample as highly potent until analytically verified. Uneven spraying onto herb can create ‘hot spots’ that deliver multi-milligram boluses and precipitate overdose.

    • Dose titration: For inhalation, start <1 mg and wait at least 10–15 minutes before any redose; for oral, wait ≥90 minutes. Avoid stacking doses due to delayed peaks and risk of panic, vomiting, or syncope. General harm-reduction guidance favors conservative titration with new SCRAs.

    • Mixing/solvents: If applying to plant material, dissolve a measured amount in volatile solvent (e.g., ethanol/acetone), apply evenly, tumble/mix thoroughly, and fully dry to minimize hot spots. Never sprinkle dry crystals. Community and harm-reduction groups consistently warn about dosing variability in SCRA smoking blends.

    • Toxicity profile: Outbreaks linked to ADB-PINACA involved severe agitation, confusion, hypertension and ICU admissions, highlighting a narrow safety margin even in small inhaled doses.

    • Class risk context: EMCDDA/EUDA reports for closely related SCRAs (e.g., 5F‑MDMB‑PINACA; MDMB‑4en‑PINACA) document very high CB1 potency and numerous severe poisonings and fatalities at low milligram doses; ADB‑PINACA belongs to the same indazole‑3‑carboxamide class and should be approached with identical caution.

    • Set/setting & sitter: Rapid-onset dysphoria, paranoia, and ‘white‑out’ episodes are widely reported; use with a trusted sober sitter and a quiet environment to reduce panic‑driven redosing or hazardous behavior. Harm‑reduction communities emphasize sober supervision for potent SCRAs.

    • Contraindications: Avoid if you have a history of seizures, serious cardiovascular disease, or psychosis; SCRA events frequently include seizures, tachyarrhythmias, and severe agitation.

    • Polydrug use: Combining with depressants (alcohol, opioids, benzos) increases aspiration and sedation risks if vomiting or syncope occur; combining with stimulants increases cardiac load and panic. Consult interaction charts before mixing.

    • Legal/testing: Many jurisdictions control ADB‑PINACA and analogs. Commercial immunoassays often miss specific SCRAs; only targeted LC‑MS/MS detects metabolites reliably—assume low detectability and short parent half‑life but unpredictable detection windows by lab panel. (General lab screening literature on SCRAs; variability is high.)

    • Driving/operating machinery: Wait at least 8 hours after last dose and until fully baseline; residual cognitive effects can persist into the next day in some users.

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