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Ethylisopropyltryptamine

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Ethylisopropyltryptamine
Clinical data
Other namesEiPT;N-Ethyl-N-isopropyltryptamine
Routes of
administration
Oral[1]
Drug classPsychedelic drug;Serotonergic psychedelic
ATC code
  • none
Legal status
Legal status
Pharmacokinetic data
Duration of action4–6 hours[1]
Identifiers
  • N-ethyl-N-[2-(1H-indol-3-yl)ethyl]propan-2-amine
CAS Number
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC15H22N2
Molar mass230.355 g·mol−1
3D model (JSmol)
Melting point71 to 73 °C (160 to 163 °F)
  • CCN(C(C)C)CCc1c[nH]c2ccccc12
  • InChI=1S/C15H22N2/c1-4-17(12(2)3)10-9-13-11-16-15-8-6-5-7-14(13)15/h5-8,11-12,16H,4,9-10H2,1-3H3 checkY
  • Key:HQZLBYMOYCJZRF-UHFFFAOYSA-N checkY
  (verify)

Ethylisopropyltryptamine (EiPT), also known asN-ethyl-N-isopropyltryptamine, is apsychedelic drug of thetryptamine family.[1] It is takenorally.[1]

EiPT appears to have been firstsynthesized and described byAlexander Shulgin.[1]

Use and effects

[edit]

In his bookTiHKAL (Tryptamines I Have Known and Loved),Alexander Shulgin lists the dose of EiPT as 24 to 40 mg and itsduration as 4 to 6 hours.[1] According to Shulgin, this compound tends to producenausea,dysphoria, and other unpleasantside effects.[1] It also seems to largely lack thehallucinatory andvisual properties usually associated with psychedelic drugs.[1]

Interactions

[edit]
See also:Psychedelic drug § Interactions, andTrip killer § Serotonergic psychedelic antidotes

Chemistry

[edit]

EiPT is short forN-ethyl-N-isopropyltryptamine.[1] The full chemical name of this structure isN-ethyl-N-[2-(1H-indol-3-yl)ethyl]propan-2-amine. The compound is asubstituted tryptamine, which all belong to a larger family of compounds known asindolethylamines.[1] EiPT is closely related to the compoundsdiethyltryptamine (DET) andDIPT.[1]

Synthesis

[edit]

Thechemical synthesis of EiPT has been described.[1]

Society and culture

[edit]

Legal status

[edit]

United States

[edit]

EiPT is unscheduled and uncontrolled in theUnited States, but possession and sales of EiPT could be prosecuted under theFederal Analog Act because of its structural similarities to DET.[citation needed]

See also

[edit]

References

[edit]
  1. ^abcdefghijklShulgin, Alexander;Shulgin, Ann (September 1997).TiHKAL: The Continuation.Berkeley, California:Transform Press.ISBN 0-9630096-9-9.OCLC 38503252.https://www.erowid.org/library/books_online/tihkal/tihkal10.shtml

External links

[edit]
Tryptamines
No ring subs.
4-Hydroxytryptamines
5-Hydroxytryptamines
5-Methoxytryptamines
Other ring subs.
α-Alkyltryptamines
Others
Cyclized
Bioisosteres
Phenethylamines
Scalines
2C-x
3C-x
DOx
4C-x
Ψ-PEA
MDxx
FLY
25x-NB (NBOMes)
Others
Cyclized
Lysergamides
  • Bioisosteres:JRT
Others
Natural sources
Tryptamines
4-Hydroxytryptamines
andesters/ethers
5-Hydroxy- and
5-methoxytryptamines
N-Acetyltryptamines
α-Alkyltryptamines
Cyclized tryptamines
Isotryptamines
Related compounds
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