DiPT
DiPT is a psychedelic substance of the tryptamine class and a structural analog of DMT.1 First described in the scientific literature in 1959, its psychoactive properties in humans were characterized by Alexander Shulgin in the mid-1970s and detailed in his 1997 book TiHKAL. DiPT is distinctive among psychedelics for producing primarily auditory rather than visual effects, including perceived shifts in pitch and harmonic distortion. Individual sensitivity varies considerably, and it has been sold as a research chemical.
Dosage & Duration
Dosage
Intensity of effects at a given dose varies widely between individuals; some users report overpowering effects at 50 mg while others report only mild effects at 100 mg. Start low to gauge individual sensitivity.
Subjective Effects
In a preliminary study of nine adult volunteers, orally administered DiPT produced a predominantly auditory syndrome. At active doses, participants commonly reported lethargy, a desire to lie down, emotional distance, little or no euphoria, and distortion of pitch and timbre. The study reported no visual-field distortion and no eyes-closed imagery.[cite:pmid-6949674]
Physical
At active oral doses in the preliminary study, lethargy and a desire to lie down were characteristic. Across the preliminary trials, two participants reported mild nausea, three reported muscular hyperreflexia, and slight pupil dilation occurred in most participants.[cite:pmid-6949674] Separate archival self-reports described ear pressure at 18 mg oral, poor handwriting at 25 mg oral, mild diarrhea five to ten hours after 100 mg oral, and tongue numbness after 8 mg smoked.[cite:url-erowid-org-tihkal04-shtml]
Uncomfortable
Cognitive
Participants in the preliminary study described distance from their surroundings or their own feelings, with little or no euphoria, and the experience was characterized as neutral rather than clearly pleasant or unpleasant.[cite:pmid-6949674] A later archival self-report at 250 mg oral described marked foreboding and an ominous, unreal quality; this high-dose report should not be generalized to usual doses.[cite:url-erowid-org-tihkal04-shtml]
Auditory
Auditory disturbance was the consistent finding of the preliminary study and, at the doses studied, essentially the entire sensory signature.[cite:pmid-6949674]
Tactile
Pharmacology
Pharmacodynamics
DiPT acts primarily as a full agonist of the serotonin 5-HT2A, 5-HT2B, and 5-HT2C receptors, with 5-HT2A activation appearing to principally mediate its psychedelic effects in animal models. It also shows weak activity at the 5-HT1A receptor and functions as a weak serotonin reuptake inhibitor. Additional binding affinities have been reported at dopamine receptors, adrenergic receptors, and the dopamine and norepinephrine transporters, though the contribution of these interactions to its overall effects remains unclear. The mechanisms underlying DiPT's characteristic selective alterations of auditory perception are unknown.
Pharmacokinetics
DiPT has not received a formal human pharmacokinetic characterization. A preliminary study in nine volunteers reported oral effects beginning after 20–30 minutes and peaking after about 1.5–2 hours, but it did not measure blood or urine concentrations, bioavailability, clearance, or elimination half-life.1 The authors of that study proposed that the bulky N-isopropyl groups might resist N-dealkylation or oxidative deamination, but explicitly framed this as a hypothesis requiring kinetic and metabolic studies.1 A 2022 Drug Enforcement Administration review likewise stated that metabolism studies had not been conducted for DiPT.8
Interactions
An unlisted combination is an unknown one, not a safe one. Check a dedicated combination chart before mixing.
Tolerance
Serotonergic psychedelics
Harm Potential
Addiction & Dependence
Psychological
Extremely LowDiPT is not habit-forming and the desire to use it can actually decrease with use. It is described as most often self-regulating.
Physical
No information exists regarding physical dependence or withdrawal symptoms. Unusually among psychedelics, DiPT did not show evidence of behavioral tolerance in rodent studies.9
Toxicity
DiPT is known to chronically alter the perception of sound and speech in some users, which may persist beyond the acute effects; ear pressure ranging from mild to painful has been reported, particularly when combined with MDMA.
Psychosis Risk
At typical doses, DiPT is described as producing lucid and clear-headed cognitive effects compared to other tryptamines. At very high doses (250mg), one report described delusional spiritual experiences including feeling spoken to by spirits and perceiving an 'anti-universe.'11 Confusion has been noted at higher doses.
Seizure Risk
DiPT produces convulsions at high doses in rodent studies.7 No human seizure cases are documented in the available literature.
History & Culture
Discovery and Development
DiPT was first characterized in the scientific literature by R.B. Barlow and colleagues in 1959.12 Alexander Shulgin began investigating the compound's effects in humans during the mid-1970s, with his initial findings dating to 1974 and basic properties…
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Legality
By Country
References
Source Pages
Citations
- A T Shulgin, & M F Carter. (1980). N, N-Diisopropyltryptamine (DIPT) and 5-methoxy-N,N-diisopropyltryptamine (5-MeO-DIPT). Two orally active tryptamine analogs with CNS activity. Communications in Psychopharmacology, 4(5), 363–369. https://bibliography.maps.org/resources/download/88441234567891011121314151617181920
- dose.wiki generation draft: dipt__dosage_duration.yaml, 24 July 2026, lines 53-104. github.com (n.d.). https://github.com/josikinzz/dosewiki-admin/blob/main/runs/gap-generation-2026-07-24/drafts/wave-02/dipt__dosage_duration.yaml#L53-L10412
- dose.wiki earlier article export: DiPT, 2 August 2026, lines 43-59. github.com (n.d.). https://github.com/josikinzz/dosewiki-admin/blob/main/runs/article-review-2026-08-02/articles/dipt.md#L43-L5912
- PsychonautWiki. psychonautwiki.org (n.d.). https://psychonautwiki.org/wiki/DiPT12
- DiPT structured drug record. tripbot.tripsit.me (n.d.). https://tripbot.tripsit.me/api/tripsit/getDrug/dipt12
- Bruce E. Blough, Antonio Landavazo, Ann M. Decker, John S. Partilla, Michael H. Baumann, & Richard B. Rothman. (October 2014). Interaction of psychoactive tryptamines with biogenic amine transporters and serotonin receptor subtypes. Psychopharmacology, 231(21), 4135–4144. https://doi.org/10.1007/s00213-014-3557-71
- Michael B. Gatch, Michael J. Forster, Aaron Janowsky, & Amy J. Eshleman. (July 2011). Abuse liability profile of three substituted tryptamines. The Journal of Pharmacology and Experimental Therapeutics, 338(1), 280–289. https://doi.org/10.1124/jpet.111.17970512
- Drug Enforcement Administration. federalregister.gov (n.d.). https://www.federalregister.gov/documents/full_text/text/2022/01/14/2022-00713.txt12
- Douglas A. Smith, Jessica M. Bailey, Diarria Williams, & William E. Fantegrossi. (December 2014). Tolerance and cross-tolerance to head twitch behavior elicited by phenethylamine- and tryptamine-derived hallucinogens in mice. J Pharmacol Exp Ther, 351(3), 485–491. https://doi.org/10.1124/jpet.114.2193371
- Simon L. Hill, & Simon H. L. Thomas. (October 2011). Clinical toxicology of newer recreational drugs. Clinical Toxicology, 49(8), 705–719. https://doi.org/10.3109/15563650.2011.6153181
- TiHKAL: Tryptamines I Have Known and Loved. 403–406 (1997). https://www.erowid.org/library/books_online/tihkal/tihkal04.shtml123456789101112131415161718
- R. B. BARLOW, & I. KHAN. (March 1959). Actions of some analogues of tryptamine on the isolated rat uterus and on the isolated rat fundus strip preparations. British Journal of Pharmacology and Chemotherapy, 14(1), 99–107. https://doi.org/10.1111/j.1476-5381.1959.tb00934.x1
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- Schedules of Controlled Substances: Placement of 4-OH-DiPT, 5-MeO-AMT, 5-MeO-MiPT, 5-MeO-DET, and DiPT in Schedule I; Withdrawal of Proposed Rule and Notice of Hearing. Drug Enforcement Administration, Federal Register Vol. 87, No. 143 (July 27, 2022) (n.d.). https://www.govinfo.gov/content/pkg/FR-2022-07-27/pdf/2022-16102.pdf1
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