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    CBC molecular structure

    CBC Stats & Data

    NPS DataHub
    MW314.47
    FormulaC21H30O2
    CAS20675-51-8
    IUPAC2-methyl-2-(4-methylpent-3-enyl)-7-pentylchromen-5-ol
    SMILESCCCCCc1cc(O)c2C=CC(C)(CCC=C(C)C)Oc2c1
    InChIKeyUVOLYTDXHDXWJU-UHFFFAOYSA-N
    Chemical Class Cannabinoid
    Psychoactive Class Depressant
    Half-Life Animal data suggest low-hour range (approx. 1–4 h) with lipophilic tissue retention; human half-life not formally characterized.

    Pharmacology

    DrugBank

    Toxicity

    PsychonautWiki

    Despite its reputation for being a benign substance, it is important to be aware that cannabis use is associated with distinct risks. Acute adverse effects include anxiety, hyperemesis syndrome, impaired coordination and judgment, suicidal ideations/tendencies, and psychotic symptoms.

    Addiction & dependence

    Cannabis is moderately habit-forming. Research has shown the overall dependence potential for cannabis to be less than that for caffeine, tobacco, alcohol, cocaine or heroin, but higher than that for psilocybin, mescaline, or LSD. Dependence on cannabis is more common amongst heavy users.

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Animal data suggest low-hour range (approx. 1–4 h) with lipophilic tissue retention; human half-life not formally characterized.
    Addiction Potential
    Very low. No reinforcing effects observed in animal paradigms for non-intoxicating cannabinoids and no human case reports of dependence specific to CBC; overall profile comparable to CBD rather than THC.

    Tolerance Decay

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

    No controlled human data. Tolerance, if any, appears to build slowly with daily use and decays over weeks, extrapolated from general cannabinoid exposure patterns and user reports.

    Cross-Tolerances

    Other cannabinoids (partial)
    30% ●○○

    Harm Reduction

    drugs.wiki

    CBC is a rare, non-intoxicating cannabinoid present at low levels in Cannabis sativa. In vitro work shows CBC acts as a potent agonist at TRPA1 channels and can desensitize TRP channels, which aligns with analgesic and anti-inflammatory signals in preclinical models; however, TRPA1 activation is also linked to burning/irritant sensations in humans, so inhalation can cause throat or airway irritation in sensitive users. Human pharmacology data remain sparse; most information comes from animal experiments and user reports from CBC isolates (tinctures, vape cartridges). Because several phytocannabinoids (e.g., THC, CBD, CBN) inhibit major drug‑metabolizing CYP enzymes in vitro (notably 2C9, 2C19, 2D6, 3A4), and specific CBC interaction data are limited, medications with a narrow therapeutic index metabolized by these enzymes (such as warfarin for CYP2C9) warrant extra caution and monitoring. Avoid vape products containing vitamin E acetate or other oil diluents not intended for inhalation; vitamin E acetate has been identified by European early warning systems as a high‑concern substance when inhaled. For oral use, high‑fat meals can markedly increase cannabinoid exposure (demonstrated for CBD), so keep meal patterns consistent to avoid unintended dose escalation. High‑dose CBD can elevate liver enzymes; while this has not been demonstrated for CBC, prudence suggests caution with pre‑existing liver disease or when combining multiple cannabinoids over long periods. Until individual response is known, avoid driving or operating machinery after dosing, and avoid combining with other CNS depressants. Prefer regulated or lab‑tested products and, where available, consider drug checking services to reduce contamination risks. Storage away from heat and light is advisable as cannabinoids can degrade under harsh conditions, although human‑relevant CBC degradation pathways are not well characterized.

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