DiPT

DiPT

DiPT

Psychoactive Research chemicals are new synthetic substances that are structurally similar to the original drug, while being functional analogs. Research on the effects of, and treatment for, abuse of these drugs is limited due to the fact that they’re fairly new and have avoided mainstream notice. Research chemicals do not have a lot of human consumption data, and thus harm-reduction and special care should be taken if choosing to ingest them.

Psychedelics are drugs which cause profound changes in a one’s perceptions of reality, otherwise known as hallucinations. While under the influence of hallucinogens, users might see images, hear sounds or feel sensations. These chemicals offer some of the most intense psychological experiences and care should be taken when ingesting them.

Disclaimer: Psychedelic drugs offer some of the most power and intense psychological experiences. Additionally these substances are illegal in many places. We understand that even though these substances are illegal, their use occurs frequently. We do not condone breaking of the law. By providing accurate information about these substances, we encourage the user to make responsible decisions and practice harm reduction.

Read the full disclaimer here.

Practice Harm Reduction. Proceed with Caution.

Description

DiPT

Also known as:

  • 1H-Indole-3-ethanamine, N,N-bis(1-methylethyl)-[ACD/Index Name]
  • INDOLE, 3-(2-(DIISOPROPYLAMINO)ETHYL)-
  • N,N-diisopropyltryptamine
  • N,N-Diisopropyltryptamine(DIPT)
  • N-[2-(1H-Indol-3-yl)ethyl]-N-isopropyl-2-propanamin[German][ACD/IUPAC Name]
  • N-[2-(1H-Indol-3-yl)ethyl]-N-isopropyl-2-propanamine[ACD/IUPAC Name]
  • N-[2-(1H-Indol-3-yl)éthyl]-N-isopropyl-2-propanamine[French][ACD/IUPAC Name]
  • N-[2-(1H-Indol-3-yl)ethyl]-N-isopropylpropan-2-amine
  • [2-(1H-INDOL-3-YL)ETHYL]BIS(PROPAN-2-YL)AMINE
  • 1H-Indole-3-ethanamine,N,N-bis(1-methylethyl)-
  • 3-(2-Diisopropylaminoethyl) indole
  • D-4230
  • Diisopropyltryptamine[ACD/IUPAC Name]
  • DIPT
  • MFCD09033197
  • N-(2-(1H-Indol-3-yl)ethyl)-N-isopropylpropan-2-amine
  • N,N-bis(1-methylethyl)-1H-indole-3-ethanamine
  • N,N-Diisopropyltryptamine free base
  • N,N-Diisopropyltryptamine, free base
  • N-[2-(1H-indol-3-yl)ethyl]-N-(1-methylethyl)propan-2-amine
  • N-[2-(1H-indol-3-yl)ethyl]-N-(propan-2-yl)propan-2-amine[ACD/IUPAC Name]
  • N-[2-(1H-indol-3-yl)ethyl]-N-propan-2-ylpropan-2-amine

A rare tryptamine psychedelic closely related to DMT, with the interesting property of having little visual hallucinations, but strong auditory effects.

Summary

It is a structural analog of DMT and related to various psychedelic tryptamines such as 4-HO-DiPT, 5-MeO-DiPT, and MiPT. The first human trials of DiPT were undertaken in 1975 by Alexander Shulgin, who would co-author and publish a paper detailing its synthesis and human psychopharmacology in 1981. A summary of the synthesis and reports of human use is included in Shulgin's 1997 book TiHKAL ("Tryptamines I Have Known And Loved").

It has been sold online as a research chemical. While most psychedelics are known for producing vivid visual distortions, DiPT’s effects are reported to be primarily auditory in nature. Anecdotal reports have described it causing a downward shift in perceived pitch and other unusual distortions.

It has been suggested that DiPT may have value in neurological research due to its unique effects on auditory perception. Additional subjective effects of DiPT include a body high, moderate euphoria, mild visuals, dizziness, and nausea. Very little data exists about the pharmacological properties, metabolism, and toxicity of DiPT, and it has a limited history of human use.

It is highly advised to use harm reduction practices if using this substance.

History

Chemistry

DiPT

DiPT

Tryptamines share a core structure comprised of a bicylic indole heterocycle attached at R3 to an amino group via an ethyl side chain. DiPT also contains two isopropyl groups bound to the terminal amine RN of its tryptamine backbone.

Isopropyl groups are a three carbon (propyl) chain bound at the middle carbon to the chemical structure.

DiPT has substituted analogues such 5-MeO-DiPT. DiPT is analogous to DMT, containing two isopropyl groups bound at RN instead of the two methyl groups found in DMT.

Common NameN,N-diisopropyltryptamine
Systematic nameN,N-diisopropyltryptamine
FormulaC_{16}H_{24}N_{2}
SMILESCC(C)N(CCc1c[nH]c2c1cccc2)C(C)C
Std. InChiInChI=1S/C16H24N2/c1-12(2)18(13(3)4)10-9-14-11-17-16-8-6-5-7-15(14)16/h5-8,11-13,17H,9-10H2,1-4H3
Std. InChiKeyZRVAAGAZUWXRIP-UHFFFAOYSA-N
Avg. Mass244.3752 Da
Molecular Weight244.3752
Monoisotopic Mass244.193954 Da
Nominal Mass244
ChemSpider ID25060

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Dosing Guide

Threshold:
Threshold15mg
Light15-25mg
Common30-50mg
Heavy50mg+

Duration

DiPT Duration Data
Onset30-60 minutes
Duration3-5 hours
After-effects12-24 hours

Interactions and Synergies

There are no existing interaction or synergy data for this drug.

General Information

Experiences
Oral
Vaporization
Come up
Dosage
EffectsEuphoria, empathy, insight, brightened colour, Closed/Open eye visuals, enhanced tactile sensation, mental/physical stimulation, decreased appetite, pupil dilation, restlessness, change in perception, ego softening, sweating/chills, muscle tension, confusion, insomnia.
After Effects
Avoid
Warning
Risks
Test Kits
Marguis Test Result
Tolerance
Detection
Half-life
Advice
Note
Note 2:
Note 3:

Effects

Pharmacological Effects

The psychedelic effects of DiPT are believed to come from its efficacy at the 5-HT2A receptor. However, the role of these interactions and how they result in the psychedelic experience remains subject to on-going scientific investigation.

Subjective Effects

Physical Effects

Psychological Effects

The cognitive effects of DiPT are reportedly very lucid and clear-headed in comparison to most other tryptamines.

Visual Effects

The sensory effects of DiPT are mostly auditory, however may still produce visual effects, in a similar fashion to other serotonergic psychedelics, especially at higher dosages These effects can include:

Auditory Effects

There is much speculation as to the nature of DiPT's aural distortion. At lower dosages, it has been reported to have an effect similar to a flanging, or a phase shift. At medium and higher dosages, the effect of DiPT is typically a radical shift downward in perceived pitch. This shift also tends to be nonlinear in that the shift downwards varies in relation to the initial pitch, for example, higher pitches are not lowered as much as already low pitches. This can produce bizarre sounds and render music disharmonious or unrecognizable These auditory effects of DiPT are very apparent in their occurrence and exhibit a full range of effects which commonly includes:

Sensory Effects

Transpersonal Effects

Legal Status

  • Germany: DiPT is controlled under the NpSG (New Psychoactive Substances Act) as of July 18, 2019. Production and import with the aim to place it on the market, administration to another person and trading is punishable. Possession is illegal but not penalized.
  • Latvia: DiPT is a Schedule I controlled substance.
  • New Zealand: DiPT is an analogue of DMT, so is a Class C controlled controlled substance in New Zealand.
  • United Kingdom: DiPT is a Class A controlled substance in the United Kingdom as a result of the tryptamine catch-all clause.
  • United States: DiPT is unscheduled in the United States. It may be considered an analogue of DET, a Schedule I compound under the Controlled Substances Act. As such, the sale for human consumption or the use for illicit non-medical or industrial intents and purposes could be prosecuted as crimes under the Federal Analogue Act.
    • Florida: DiPT is a Schedule I controlled substance in the state of Florida. It is illegal to buy, sell, or possess.

  • References

    1. Alexander Shulgin. Pharmacology Notes I (The Shulgin Lab Books) (PDF). Erowid. p. 177.
    2. Shulgin, A. T.; Carter, M. F. (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.  0145-5699. OCLC 3012956. PMID 6949674.
    3. Shulgin, Alexander; Shulgin, Ann (1997). TiHKAL: The Continuation. United States: Transform Press.  0-9630096-9-9. OCLC 38503252.
    4. Shulgin & Shulgin 1997, p. 403–406.
    5. "Anlage NpSG" (in German). Bundesministerium der Justiz und für Verbraucherschutz [Federal Ministry of Justice and Consumer Protection]. Retrieved December 10, 2019.
    6. "Verordnung zur Änderung der Anlage des Neue-psychoaktive-Stoffe-Gesetzes und von Anlagen des Betäubungsmittelgesetzes" (PDF). Bundesgesetzblatt Jahrgang 2019 Teil I Nr. 27 (in German). Bundesanzeiger Verlag. July 17, 2019. pp. 1083–1094. Retrieved January 1, 2020.
    7. "§ 4 NpSG" (in German). Bundesministerium der Justiz und für Verbraucherschutz [Federal Ministry of Justice and Consumer Protection]. Retrieved December 10, 2019.
    8. "Noteikumi par Latvijā kontrolējamajām narkotiskajām vielām, psihotropajām vielām un prekursoriem" (in Latvian). VSIA Latvijas Vēstnesis. November 10, 2005. Retrieved January 1, 2020.
    9. "Schedule 1 Class A controlled drugs". "Reprint as at 13 August 2019: Misuse of Drugs Act 1975". Parliamentary Counsel Office. Retrieved January 7, 2020.
    10. "Part I: Class A Drugs". "Misuse of Drugs Act 1971". UK Government. Retrieved January 7, 2020.
    11. The 2015 Florida Statutes | http://leg.state.fl.us/statutes/index.cfm?App_mode=Display_Statute&URL=0800-0899/0893/0893.html

    Resources

    1. AKos AKOS015967146
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    Sources

    Information made possible with:

    1. PsychonautWiki is a community-driven online encyclopedia that aims to document the field of psychonautics in a comprehensive, scientifically-grounded manner.
    2. Erowid is a non-profit educational & harm-reduction resource with 60 thousand pages of online information about psychoactive drugs
    3. PubChem National Center for Bio Informatics
    4. Chemspider is a free chemical structure database providing fast access to over 34 million structures, properties and associated information.
    5. Wikipedia

    Additional APIs were used to construct this information. Thanks for ChemSpider, NCBI, PubChem etc.

    Data is constantly updated so please check back later to see if there is any more available information on this substance.