Home
    Disclaimer

    MXiPr Stats & Data

    Mxip Isopropyxetamine 3-meo-2-oxo-pcipr Isopropyloxetamine 3-methoxy-2-oxo-pcipr
    NPS DataHub
    MW297.82
    FormulaC16H24ClNO2
    IUPAC(R/S)-2-(3-Methoxyphenyl)-2-(isopropylamino)cyclohexanone
    SMILES[Cl-].COc1cccc(c1)C1(CCCCC1=O)NC(C)C.[H+]
    InChIKeyOOLSOYRWBLRTLT-UHFFFAOYSA-N
    Arylcyclohexylamines; 2021/6. Von Arylcyclohexylamin abgeleitete Verbindungen; 2022/6. Von Arylcyclohexylamin abgeleitete Verbindungen
    Psychoactive Class Dissociative
    Half-Life Unknown in humans; subjective effect window typically 2–5 h depending on route.

    Effect Profile

    Curated + 8 Reports
    Dissociative 5.1

    Strong dissociative depth, mania, and motor impairment with low insight

    Dissociative Depth×3
    10
    Mania / Compulsion×1
    10
    Insight / Novel Thought×2
    3
    Motor / Sensory Impairment×1
    10

    Duration Timeline

    Bluelight
    Onset Comeup Peak Offset After Effects
    Oral
    15-45 minutes
    30 minutes - 1.0 hours
    45 minutes - 2.0 hours
    1-2 hours
    1-3 hours
    Insufflated
    4-15 minutes
    15-30 minutes
    45 minutes - 1.5 hours
    1-2 hours
    1-3 hours

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Unknown in humans; subjective effect window typically 2–5 h depending on route.
    Addiction Potential
    Moderate; several users describe compulsive redosing reminiscent of MXE/ketamine. Avoid frequent use and pre-plan limits.

    Tolerance Decay

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

    Rapid acute tolerance is commonly reported within sessions; inter-session tolerance declines over 1–3 weeks. Data are anecdotal and extrapolated from ketamine/MXE patterns.

    Cross-Tolerances

    ketamine
    60% ●○○
    MXE
    60% ●○○
    other arylcyclohexylamines
    50% ●○○

    Experience Report Analysis

    Erowid
    8 Reports
    2020–2024 Date Range
    8 With Age Data
    13 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid

    Effects aggregated from 8 experience reports (8 Erowid)

    8 Reports
    13 Effects Detected
    8 Positive
    1 Adverse
    4 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 8

    Euphoria 87.5% 70%
    Music Enhancement 62.5% 70%
    Color Enhancement 50.0% 70%
    Empathy 50.0% 70%
    Focus Enhancement 50.0% 70%
    Body High 50.0% 70%
    Stimulation 50.0% 70%
    Tactile Enhancement 37.5% 70%

    Adverse Effects 1

    Confusion 37.5% 70%

    Real-World Dose Distribution

    62K Doses

    From 10 individual dose entries

    Insufflated (n=8)

    Median: 45.0mg 25th: 30.0mg 75th: 52.5mg 90th: 60.0mg
    mg/kg median: 0.737 mg/kg 75th: 0.882

    Form / Preparation

    Most common forms and preparations reported

    Harm Reduction

    drugs.wiki

    Naming clarity reduces mix-ups: MXiPr is 3-MeO-2′-oxo-PCiPr (IUPAC: 2-(isopropylamino)-2-(3-methoxyphenyl)cyclohexan-1-one); some vendors list it as “methoxipropamine.” Verify the label and test a tiny allergy dose before real dosing. Evidence: vendor and user discussions on Bluelight.

    Injectable routes: multiple community reports describe seizures at very high intramuscular doses (≈80–100 mg+). Because this compound lacks human PK/PD data and sterile formulation guidance, avoid IM/IV; if someone ignores this advice, using clinical-grade sterile technique and conservative dosing is critical. Evidence: recent user thread collating seizure reports.

    CNS depressants (alcohol, opioids, benzos, GHB/GBL) markedly increase risks of blackout, aspiration, and respiratory depression with ketamine-like dissociatives; treat these combos as dangerous. Evidence: TripSit combination guidance (ketamine proxies).

    Stacking dissociatives (e.g., DXM, nitrous, ketamine analogues) can amplify ataxia, delirium, hypoxia, and amnesia. If nitrous is used, keep sessions brief, seated, and spaced—heavy or repeated nitrous exposure inactivates vitamin B12 and can cause neuropathy. Evidence: TripSit combos; DrugWise/EUDA nitrous overview.

    Seizure-threshold–lowering medicines (tramadol, bupropion) warrant extra caution; avoid high doses and combinations that add sleep deprivation or stimulants. Evidence: StatPearls/LiverTox monographs.

    Nasal care for insufflation: finely crush, use your own clean straw, rinse with water before/after, alternate nostrils, and rest your nose to reduce bleeding and septal injury. Evidence: Hi‑Ground harm‑reduction pages.

    Bladder and biliary risks: heavy/frequent arylcyclohexylamine use (well-documented for ketamine) can lead to ulcerative cystitis and, more rarely, hepatobiliary injury. Space sessions (weeks, not days), hydrate, and stop use if urinary urgency/pain or right‑upper‑quadrant pain occurs; seek medical evaluation. Evidence: StatPearls and LiverTox.

    Impairment: dissociatives robustly impair coordination and judgment; plan a safe setting, sober sitter at high doses, and no driving/operating machinery until the following day. Evidence: StatPearls; DrugWise.

    Drug checking: the unregulated market shows frequent mislabeling and adulteration across dissociative/stimulant categories. Use a trusted drug‑checking service where available; reagent tests are helpful but may not distinguish closely related arylcyclohexylamines. Evidence: EUDA DIMS report; Toronto Drug Checking Service.

    Compulsive redosing risk: many users report rapid tolerance and habit-forming patterns similar to MXE. Set firm maximums per session and leave multi-day washouts to mitigate escalation. Evidence: Bluelight MXiPr thread.

    ← Back to MXiPr