World Library  
Flag as Inappropriate
Email this Article

Dipropyltryptamine

Article Id: WHEBN0000362970
Reproduction Date:

Title: Dipropyltryptamine  
Author: World Heritage Encyclopedia
Language: English
Subject: N-Methyltryptamine, 5-MeO-DMT, ETH-LAD, 5-MeO-aMT, O-Acetylpsilocin
Collection: Designer Drugs, Entheogens, Psychedelic Tryptamines, Serotonin Receptor Agonists, Serotonin Releasing Agents
Publisher: World Heritage Encyclopedia
Publication
Date:
 

Dipropyltryptamine

Dipropyltryptamine
Systematic (IUPAC) name
3-[2-(dipropylamino)ethyl]indole
Clinical data
Legal status
Routes of
administration
Ingestion, inhalation, intravenous or intramuscular injection
Identifiers
CAS Registry Number  Y
ATC code None
PubChem CID:
ChemSpider  Y
Chemical data
Formula C16H24N2
Molecular mass 244.38 g/mol
Physical data
Melting point 174.5 to 178 °C (346.1 to 352.4 °F)
 Y   

N,N-Dipropyltryptamine (DPT, also known as "The Light") is a psychedelic drug belonging to the tryptamine family, first reported in 1973.[1] It is found either as its crystalline hydrochloride salt or as an oily or crystalline base. It has not been found to occur naturally.

Frequent physical effects are nausea, numbness of the tongue or throat, and pupil dilation.

Contents

  • Pharmacology 1
  • Chemistry 2
  • Psychedelic properties 3
  • Side Effects 4
  • Religious use 5
  • Legal status 6
    • United Kingdom 6.1
    • United States 6.2
      • Florida 6.2.1
      • Maine 6.2.2
  • References 7
  • External links 8

Pharmacology

Studies on rodents have found that the effectiveness with which a selective 5-HT2A receptor antagonist blocks the behavioral actions of this compound strongly suggest that the 5-HT2A receptor is an important site of action for DPT, but the modulatory actions of a 5-HT1A receptor antagonist also imply a 5-HT1A-mediated component to the actions of DPT.[2]

Chemistry

DPT changes Ehrlich's reagent violet and causes the marquis reagent to turn yellow.[3]

Psychedelic properties

While dipropyltryptamine is chemically similar to dimethyltryptamine (DMT), its psychoactive effects are markedly different.[4]

The most prominent features of the DPT experience are increased significance or intensity of music, colors take on a new intensity or appearance, the body may have a buzz or vibratory feeling, a pleasant sensation of warmth, complete ego loss, apparitions of faces.

While seeing other beings under the influence of DPT may occasionally occur, the perspective is more as an observer or watcher, as contrasted to the more personal real-feeling entity contact reported with DMT.[5]

Also sometimes reported is a loss of ego boundary; for example, the boundary between the self and a table may not be easy to distinguish. Difficulty distinguishing other boundaries is common as well. For example, different colors may be difficult to distinguish. Other sensory input may also become blended. This is distinct from synaesthesia.

A user may also encounter the feeling of experiencing the life of someone else, or having had all possible experiences simultaneously. One may have the experience of seeing the universe from different locations in space and time.

Visuals are often geometric, wavy, and/or spiraled. Other visual distortions and hallucinations tend to be experienced in the peripheral vision. The self or the environment may take on a stylized cartoon-like look or feel. Pleasant flashes of light and sparkles are also common.

Side Effects

Negative side effects of human consumption of this drug (or drug being sold as DPT on the internet) can include seizures, increased heart rate, dizziness, nausea, and death.

Religious use

DPT is used as a religious sacrament by the Temple of the True Inner Light, a New York City offshoot of the Native American Church. The Temple believes DPT and other entheogens are physical manifestations of God.[6]

Legal status

United Kingdom

DPT is a Class A drug in the United Kingdom, making it illegal to possess or distribute .

United States

DPT is not scheduled at the federal level in the United States,[7] but it could be considered an analog of 5-MeO-DiPT, DMT, or DET, in which case purchase, sale, or possession could be prosecuted under the Federal Analog Act.

Florida

"DPT (N,N-Dipropyltryptamine)" is a Schedule I controlled substance in the state of Florida making it illegal to buy, sell, or possess in Florida.[8]

Maine

DPT is a Schedule I controlled substance in the state of Maine making it illegal to buy, sell, or possess in Maine.

References

  1. ^ International Pharmacopsychiatry. 1973;8(1):104.
  2. ^ William E. Fantegrossi, Chad J. Reissig, Elyse B. Katz, Haley L. Yarosh, Kenner C. Rice, Jerrold C. Winterb. Hallucinogen-like effects of N,N-dipropyltryptamine (DPT): possible mediation by serotonin 5-HT1A and 5-HT2A receptors in rodents. Pharmacol Biochem Behav. 2008 January; 88(3): 358–365.
  3. ^ Spratley, Trinette (2004). "Analytical Profiles for Five "Designer" Tryptamines" (PDF). Microgram Journal 3 (1-2): 55. Retrieved 2013-10-09. 
  4. ^  
  5. ^  
  6. ^ Temple of the True Inner Light
  7. ^ 21 CFR — SCHEDULES OF CONTROLLED SUBSTANCES §1308.11 Schedule I.
  8. ^ Florida Statutes - Chapter 893 - DRUG ABUSE PREVENTION AND CONTROL

External links

  • TiHKAL entry
  • DPT entry in TiHKAL • info
  • A DPT Primer by Toad
  • Erowid Experience Vault
This article was sourced from Creative Commons Attribution-ShareAlike License; additional terms may apply. World Heritage Encyclopedia content is assembled from numerous content providers, Open Access Publishing, and in compliance with The Fair Access to Science and Technology Research Act (FASTR), Wikimedia Foundation, Inc., Public Library of Science, The Encyclopedia of Life, Open Book Publishers (OBP), PubMed, U.S. National Library of Medicine, National Center for Biotechnology Information, U.S. National Library of Medicine, National Institutes of Health (NIH), U.S. Department of Health & Human Services, and USA.gov, which sources content from all federal, state, local, tribal, and territorial government publication portals (.gov, .mil, .edu). Funding for USA.gov and content contributors is made possible from the U.S. Congress, E-Government Act of 2002.
 
Crowd sourced content that is contributed to World Heritage Encyclopedia is peer reviewed and edited by our editorial staff to ensure quality scholarly research articles.
 
By using this site, you agree to the Terms of Use and Privacy Policy. World Heritage Encyclopedia™ is a registered trademark of the World Public Library Association, a non-profit organization.
 


Copyright © World Library Foundation. All rights reserved. eBooks from Project Gutenberg are sponsored by the World Library Foundation,
a 501c(4) Member's Support Non-Profit Organization, and is NOT affiliated with any governmental agency or department.