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    4Cl-iBF molecular structure

    4Cl-iBF Stats & Data

    P-chloro-isobutyrylfentanyl Para-chloroisobutyrylfentanyl
    NPS DataHub
    MW384.95
    FormulaC23H29ClN2O
    CAS244195-34-4
    IUPACN-(4-chlorophenyl)-2-methyl-N-[1-(2-phenylethyl)piperidin-4-yl]propanamide
    SMILESCC(C)C(=O)N(C1CCN(CCc2ccccc2)CC1)c1ccc(Cl)cc1
    InChIKeyYWHLYGSHOQKCJG-UHFFFAOYSA-N
    Phenethylamines Opioids
    Chemical Class Anilidopiperidine
    Psychoactive Class Depressant

    Effect Profile

    Curated
    Opioid 7.0

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

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

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Unknown in humans; by analogy to fentanyl analogues likely on the order of hours. Treat as unpredictable and avoid redosing within the first hour after onset.
    Addiction Potential
    Very high — comparable to other fentanyl analogues. Rapid tolerance, strong reinforcement and severe physical dependence are consistently reported in case series and surveillance reports.

    No tolerance chart. Our decay curves for opioids were estimates, and a curve can make tolerance look longer-lasting than it is, which is the dangerous direction.

    Opioid tolerance drops fast when you stop, and even a few days off can be enough, so a dose that used to be normal can now stop your breathing. Overdose deaths rise sharply after prison, detox or leaving treatment, and tolerance also falls during a hospital stay. After any break, start with a much smaller amount, try a test dose first, don't use alone, and keep naloxone within reach. Alcohol, benzodiazepines, gabapentinoids and other sedatives make an opioid overdose much more likely.

    Sources: FRANK: heroin · National Harm Reduction Coalition · WHO: opioid overdose · Merrall et al. 2010 · Binswanger et al. 2007 · Strang et al. 2003 · FDA 2019: gabapentinoids and breathing

    Cross-Tolerances

    All μ‑opioid agonists (morphine, oxycodone, heroin, fentanyl family)

    Harm Reduction

    drugs.wiki

    • Extreme potency: doses are in micrograms. Consumer‑grade 0.001 g (1 mg) scales are not reliable at this range; even 0.1 mg readability devices may be inaccurate. Use volumetric dosing: dissolve a known mass into a measured volume and measure doses by volume; label concentrations. Never eyeball powder.

    • Combining with other depressants (alcohol, benzodiazepines, Z‑drugs, GHB/GBL) markedly raises the risk of fatal respiratory depression; avoid these combinations.

    • Gabapentin/pregabalin with opioids increases overdose and respiratory‑depression risk in population studies; avoid or use only under medical oversight.

    • Tramadol with opioids increases seizure and serotonin‑toxicity risk; combination is unsafe.

    • DXM with opioids is considered a dangerous combo (additive CNS depression and other risks).

    • MAOIs should be avoided for at least 14 days; caution with SSRIs/SNRIs due to rare but reported serotonin toxicity with fentanyl.

    • Rapid IV bolus of fentanyl‑class drugs can precipitate chest‑wall rigidity and difficult ventilation; if someone injects despite risks, slow, incremental administration reduces (but does not eliminate) risk.

    • Naloxone reverses toxicity but may require repeated doses or infusion for potent/longer‑acting opioids; always call emergency services and monitor after reversal.

    • Test strips: common FTS detect fentanyl and certain analogues but not all; they give a binary result and cannot quantify potency. A negative does not guarantee safety; a positive does not reveal which analogue.

    • Unregulated opioid samples often contain benzodiazepine‑related drugs or ultra‑potent opioids (e.g., nitazenes), massively increasing overdose risk. Do not use alone; have naloxone present and a trained observer.

    • Safer‑use injection practices (if used): sterile equipment, use a needle/syringe program, rotate sites, and seek medical care early for infections.

    • Oral (swallowed) fentanyl has low bioavailability; clinically, transmucosal routes are used for fentanyl. By analogy, sublingual/buccal routes for some analogues may have higher efficiency than swallowing, but individual kinetics for 4Cl‑iBF are unknown—start low and avoid redosing during the first hour.

    • Overdose recognition: unresponsive, slow/shallow or stopped breathing, blue lips, pinpoint pupils. Call emergency services immediately; place in recovery position and administer naloxone if available.

    References

    Cited references

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