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N-tert-Butyltryptamine

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(Redirected fromN-t-Butyltryptamine)
Psychoactive drug
Pharmaceutical compound
N-tert-Butyltryptamine
Clinical data
Other namesN-t-Butyltryptamine; NtBT; NTBT
Routes of
administration
Oral[1][2]
Drug classPsychoactive drug
ATC code
  • None
Pharmacokinetic data
Duration of actionUnknown[1]
Identifiers
  • N-[2-(1H-indol-3-yl)ethyl]-2-methylpropan-2-amine
CAS Number
PubChemCID
ChemSpider
Chemical and physical data
FormulaC14H20N2
Molar mass216.328 g·mol−1
3D model (JSmol)
  • CC(C)(C)NCCC1=CNC2=CC=CC=C21
  • InChI=1S/C14H20N2/c1-14(2,3)16-9-8-11-10-15-13-7-5-4-6-12(11)13/h4-7,10,15-16H,8-9H2,1-3H3
  • Key:IDXHHISJIRGWJV-UHFFFAOYSA-N

N-tert-Butyltryptamine (NtBT) is apsychoactive drug of thetryptamine family related topsychedelics likedimethyltryptamine (DMT).[1][2][3]

Use and effects

[edit]

NtBT was briefly described byAlexander Shulgin in his bookTiHKAL (Tryptamines I Have Known and Loved).[1] According to Shulgin, NtBT is active at a dose of 5 to 20 mg or of ~20 mgorally.[1][2] He also said that he had heard that NtBT is extremelypotent whensmoked, but had not received any particulars or confirmed that.[1] Its effects included alightheadedintoxication described as a totally pleasant buzz, but nothing more profound than that.[1]

Shulgin has said that along withN-sec-butyltryptamine (NsBT), it is one of only twoN-mono-substituted tryptamines with known psychoactivity.[1] He also said thatN-mono-substituted tryptamines might beGHB-like intoxicants devoid of psychedelic effects.[1] However,N-methyltryptamine (NMT) has been reported to produce psychedelic effects.[1][4][5]

Chemistry

[edit]

Analogues of NtBT includeN-methyltryptamine (NMT),N-ethyltryptamine (NET),N-isopropyltryptamine (NiPT),N-benzyltryptamine (NBnT),4-HO-DsBT, and4-HO-McPeT, among others.[1]

See also

[edit]

References

[edit]
  1. ^abcdefghijk"N-Ethyltryptamine".TiHKAL entry. Erowid.org.The tertiary-butyl analogue, NTBT, is the remaining mono-substituted tryptamine that just might have psychotropic potential. In the 5 to 20 milligram area, there is a light-headed intoxication that is a totally pleasant buzz, but nothing more profound than that. Wouldn't it be fascination of it turned out that all of the mono-tryptamines (the NRT's) were GHB-like intoxicants, and totally devoid of psychedelic activity. That would be a true challenge to the SAR crowd. I was told many years ago that NTBT was extremely potent when smoked, but I never received any particulars, and I must leave that as a baseless rumor.
  2. ^abcShulgin AT (2003)."Basic Pharmacology and Effects". In Laing RR (ed.).Hallucinogens: A Forensic Drug Handbook. Forensic Drug Handbook Series. Elsevier Science. pp. 67–137.ISBN 978-0-12-433951-4.
  3. ^Laing RP (2003).Hallucinogens: A Forensic Drug Handbook. Academic Press. pp. 98–99.ISBN 978-0-12-433951-4.
  4. ^Nen (4 December 2011).Entheogenic effects of NMT from Acacia.Entheogenesis Australis (EGA) Conference, Victoria, Australia, 2–5 December 2011(PDF). Archived from the original on 5 April 2025. Retrieved15 April 2025.{{cite conference}}: CS1 maint: bot: original URL status unknown (link)
  5. ^Nen (13 July 2013).NMT: A Spatial Hallucinogen With Therapeutic Applications.Breaking Convention: The Second Multidisciplinary Conference on Psychedelic Consciousness, University of Greenwich, London, 12–14 July 2013.

External links

[edit]
Tryptamines
4-Hydroxytryptamines
andesters/ethers
5-Hydroxy- and
5-methoxytryptamines
N-Acetyltryptamines
α-Alkyltryptamines
Cyclized tryptamines
Isotryptamines
Related compounds
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