Home
    Disclaimer
    DiPT molecular structure

    DiPT Stats & Data

    Diisopropyltryptamine
    Chemical Class Phenethylamine
    Psychoactive Class Psychedelic
    Half-Life Not well-established in humans; functional effects typically span several hours.

    Receptor Profile

    Receptor Actions

    Agonists
    5-HT2A receptor agonist (full)
    5-HT2B receptor agonist (full)
    5-HT2C receptor agonist (full)
    Inhibitors
    Serotonin reuptake inhibitor (weak)

    History & Culture

    1959–1997

    DiPT was first characterized in the scientific literature by R.B. Barlow and colleagues in 1959. Alexander Shulgin began investigating the compound's effects in humans during the mid-1970s, with his initial findings dating to 1974 and basic properties disclosed in 1976. Shulgin published more detailed characterizations of DiPT alongside 5-MeO-DiPT in a 1980 journal article, followed by additional publications throughout the 1980s. A comprehensive synthesis and collection of human use reports appeared in Shulgin's 1997 book TiHKAL (Tryptamines I Have Known And Loved), which brought the compound to wider attention within the psychedelic research community. DiPT was subsequently encountered as a novel designer drug in Europe by 2005 and has since circulated online as a research chemical.

    DiPT's unusual property of producing primarily auditory rather than visual effects has generated interest for potential neurological research applications. Shulgin speculated that the compound might serve as a valuable tool for studying the auditory system, potentially helping to locate the pitch-processing center of the brain if combined with imaging techniques such as positron emission tomography. A small study was conducted administering DiPT to two individuals with perfect pitch to investigate whether any systematic relationship existed between a note's actual pitch and the perceived pitch under the drug's influence. The results revealed no meaningful correlation, though they reinforced observations that the pitch decrease produced by DiPT is not linear and involves genuine harmonic distortion rather than a simple uniform pitch shift.

    Effect Profile

    Curated + 100 Reports
    Psychedelic 6.9

    Strong visuals, auditory effects, and body load with mild headspace

    Visual Intensity×3
    10102.4
    Headspace Depth×3
    56.01.6
    Auditory Effects×1
    10106.2
    Body Load / Somatic Effects×1
    109.23.5
    Catalog Erowid BlueLight

    Duration Timeline

    Bluelight
    Onset Comeup Peak Offset After Effects
    Oral
    19 minutes - 1.0 hours
    30 minutes - 1.0 hours
    2-4 hours
    2-4 hours
    24 hours
    Total: 3-5 hours
    Smoked
    6-12 minutes
    12-24 hours
    Total: 15-60 minutes hours

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Not well-established in humans; functional effects typically span several hours.
    Addiction Potential
    Low; not considered habit-forming, with little evidence of compulsive use.

    Tolerance Decay

    Full tolerance 6h Half tolerance 3d Baseline ~7d

    Rapid tolerance typical of serotonergic psychedelics; spacing doses by 1–2 weeks minimizes attenuation. Model values are heuristic from community reports (anecdotal).

    Cross-Tolerances

    Psilocybin/Psilocin
    60% ●○○
    DMT/MET/MiPT/DPT
    60% ●○○
    Lysergamides (e.g., LSD/AL-LAD)
    40% ●○○

    Experience Report Analysis

    Erowid BlueLight
    76 Reports
    1999–2025 Date Range
    17 With Age Data
    31 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid + Bluelight

    Effects aggregated from 100 experience reports (76 Erowid + 24 Bluelight)

    100 Reports
    92 Effects Detected
    35 Positive
    30 Adverse
    27 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 35

    Music Enhancement 73.7% 70%
    Body High 36.0% 79%
    Stimulation 28.0% 73%
    Euphoria 25.0% 87%
    Music Distortion 25.0% 90%
    Tactile Enhancement 21.0% 80%
    Color Enhancement 20.0% 79%
    Focus Enhancement 18.4% 70%
    Joy 16.7% 79%
    Empathy 16.0% 90%
    Introspection 15.0% 71%
    Visual Trails 12.5% 72%
    Entity Imagery 12.5% 85%
    Bliss 12.5% 78%
    Libido Enhancement 12.5% 73%
    Contentment 12.5% 85%
    Awe 8.3% 70%
    Ego Inflation 8.3% 70%
    Pain Relief 5.3% 70%
    Mystical Quality 4.2% 90%

    Adverse Effects 30

    Nausea 39.0% 88%
    Anxiety 24.0% 80%
    Confusion 23.0% 78%
    Vomiting 16.7% 91%
    Tinnitus 16.7% 88%
    Depersonalization 16.7% 76%
    Restlessness 12.5% 78%
    Dizziness 12.5% 92%
    Disrupted Sleep Architecture 12.5% 75%
    Memory Suppression 9.0% 90%
    Pupil Dilation 9.0% 76%
    Body Load 8.3% 80%
    Insomnia 8.3% 80%
    Double Vision 8.3% 90%
    Blurred Vision 8.3% 85%
    Field Narrowing 8.3% 80%
    Panic 8.3% 85%
    Fear 8.3% 85%
    Body Temperature Change 8.3% 75%
    Dry Mouth 8.3% 70%

    Dose-Response Correlation

    How effect frequency changes across dose levels

    View data table
    Effect Common (n=17)
    Auditory Effects 100.0%
    Music Enhancement 88.2%
    Visual Distortions 82.4%
    Stimulation 64.7%
    Anxiety 52.9%
    Nausea 52.9%
    Empathy 47.1%
    Euphoria 41.2%
    Confusion 41.2%
    Body High 35.3%
    Closed-Eye Visuals 29.4%
    Open-Eye Visuals 23.5%
    Tactile Enhancement 23.5%
    Focus Enhancement 23.5%
    Introspection 23.5%

    Dose–Effect Mapping

    Experience Reports

    How reported effects shift across dose tiers, based on 76 experience reports.

    Limited tier coverage — most reports fall within the Common range. Effects at other dose levels may not be represented.

    Oral dose range: 30.0–76.0 mg (median 50.0 mg)
    Effect Common (n=17)
    auditory effects
    100%
    music enhancement
    88%
    visual distortions
    82%
    stimulation
    65%
    anxiety
    53%
    nausea
    53%
    empathy
    47%
    euphoria
    41%
    confusion
    41%
    body high
    35%
    closed-eye visuals
    29%
    open-eye visuals
    24%
    tactile enhancement
    24%
    focus enhancement
    24%
    introspection
    24%
    sedation
    18%
    increased heart rate
    18%
    hospital
    18%
    color enhancement
    18%
    ego dissolution
    18%

    Showing top 20 of 25 effects

    Dosage Distribution

    Dose distribution from experience reports

    Median: 50.0 mg IQR: 30.0–76.0 mg n=31

    Real-World Dose Distribution

    62K Doses

    From 77 individual dose entries

    Oral (n=56)

    Median: 47.5mg 25th: 25.0mg 75th: 70.0mg 90th: 100.0mg
    mg/kg median: 0.545 mg/kg 75th: 0.958

    Insufflated (n=11)

    Median: 15.0mg 25th: 5.0mg 75th: 100.0mg 90th: 100.0mg
    mg/kg median: 0.085 mg/kg 75th: 1.378

    Smoked (n=6)

    Median: 14.75mg 25th: 10.5mg 75th: 19.38mg 90th: 22.5mg
    mg/kg median: 0.234 mg/kg 75th: 0.256

    Common Combinations

    Most co-occurring substances in experience reports

    Form / Preparation

    Most common forms and preparations reported

    Body-Weight Dosing

    Dose relative to body weight from reports with weight data

    Median: 0.567 mg/kg IQR: 0.417–0.989 mg/kg n=29

    Redose Patterns

    Redosing behavior across 52 reports

    7.7% Redosed
    1.1 Avg Doses
    45m Median Interval

    Legal Status

    Country Status Notes
    Germany NpSG (Controlled) Controlled under the Neue-psychoaktive-Stoffe-Gesetz (New Psychoactive Substances Act) as of July 18, 2019. Production, import with intent to distribute, administration to others, and trading are punishable offenses. Possession is prohibited but not subject to criminal penalties.
    Japan Designated Substance Controlled as a Designated Substance (Shitei-Yakubutsu) under the Pharmaceutical Affairs Law. Both possession and sale are prohibited.
    Latvia Schedule I Listed as a Schedule I controlled substance under national drug control legislation.
    New Zealand Class C Classified as a Class C controlled substance due to its structural relationship to DMT, which is covered under analogue provisions in New Zealand drug law.
    Sweden Proposed for scheduling Sweden's public health agency recommended classifying DiPT as a hazardous substance on May 15, 2019. Current legal status may have changed following this recommendation.
    Switzerland Uncontrolled Not listed under Buchstabe A, B, C, or D of controlled substances legislation. May be considered legal to possess, though sale for human consumption could still raise regulatory issues.
    United Kingdom Class A Controlled as a Class A substance under the Misuse of Drugs Act 1971 due to the tryptamine catch-all clause, which covers structurally related compounds.
    United States Unscheduled (Federal Analogue Act may apply) Federally unscheduled, though it may be considered an analogue of DET or 5-MeO-DiPT under the Controlled Substances Act. Sales for human consumption or possession with intent to ingest could potentially be prosecuted under the Federal Analogue Act. Specifically listed as Schedule I in Florida and Louisiana (since June 2013).

    Harm Reduction

    drugs.wiki

    DiPT is notable for its unique auditory distortions—often downward pitch-shifting and nonlinear harmonic distortion—while visual changes are usually mild compared with other psychedelics. The altered pitch/timbre can persist into the next day in some users; to protect hearing and reduce disorientation, avoid loud venues, high headphone volumes, and tasks requiring accurate sound localization or timing (e.g., driving). Onset can be subtle; avoid redosing during the first 2–3 hours as tolerance rises quickly and effects may surge later. People with seizure disorders, on lithium, or taking serotonergic drugs (SSRIs/SNRIs/TCAs, tramadol, DXM, 5-HTP) should avoid DiPT due to seizure or serotonin-toxicity concerns. Set/setting and a sober sitter are recommended—auditory scene distortions can impair communication and situational awareness. Use drug checking: reagent tests help confirm a tryptamine (e.g., Ehrlich), but laboratory confirmation via GC/MS (e.g., DrugsData) best verifies identity. Data on non‑oral ROAs are sparse; oral is the best-characterized and most predictable route.

    ← Back to DiPT