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    DPP-26 Stats & Data

    Db-900274 Dipipanone sulfone analogue
    Chemical Class Diphenylpropylamine
    Psychoactive Class Depressant

    Effect Profile

    Curated
    Opioid 6.3

    Strong euphoria with moderate itching/nausea, mild sedation and pain relief

    Euphoria / Warmth×3
    9
    Analgesia×2
    4
    Sedation / Relaxation×1
    5
    Itching / Nausea×1
    6

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Estimated 4–8 h (no formal PK studies; some users report next‑day sedation at higher doses).
    Addiction Potential
    Moderate–high. As a µ‑opioid agonist, it carries dependence, tolerance, and withdrawal risks; several reports frame it as maintenance-like (subtle euphoria, strong sedation) yet reinforcing for those with opioid histories.

    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

    other µ‑opioid agonists

    Harm Reduction

    drugs.wiki

    Identity/purity uncertainty: DPP‑26 is very new to the grey market; vendors have reportedly copied potency claims from dipipanone. Submit samples to a drug‑checking service when possible, and assume unknown potency until lab‑verified. Large variability in active dose has been reported within and between batches. Severe nasal causticity has been described with insufflation; users reported intense burn and irritation. From a harm‑reduction standpoint, avoid IN and especially IV routes; oral is the least risky ROA for uncertain powders. At least one user reported injection burning on a miss and only partial solubility until heating; sterile technique and proper filtration cannot eliminate unknown excipients or caustic pH risks. Compared to methiodone/IC‑26 and dipipanone, several reports describe a quicker onset than methiodone but shorter overall duration (~6–10 h), with prominent sedation and modest euphoria. Redose conservatively and wait at least 3 hours after any meaningful oral dose because peaks can be delayed; stacking increases overdose risk. Co‑use with other depressants (alcohol, benzodiazepines, GHB/GBL, gabapentinoids) markedly increases the risk of respiratory depression and fatal overdose; avoid these combinations. Potentiation by antihistamines has a history of serious harm: cyclizine can intensify opioid effects and has been linked to dangerous practices with dipipanone mixtures; avoid sedating antihistamines with DPP‑26. Methadone and some opioids can prolong QT; it is unknown if DPP‑26 does, but until pharmacology is characterized, avoid concurrent QT‑prolonging drugs/electrolyte disturbances and seek medical advice if you have cardiac risk factors. Carry naloxone and ensure others know how to use it; sedation can persist into the next day. Expect typical opioid adverse effects: constipation, pruritus, miosis, nausea; mitigate constipation proactively and avoid driving or hazardous work the day of dosing and until completely alert. Immunoassay cross‑reactivity with methadone panels is unknown; given structural similarity to methiodone/dipipanone analogues, a false positive for methadone cannot be excluded; confirmatory testing (GC‑MS/LC‑MS) would be needed.

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