5-Ethyl-DMT: Difference between revisions

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{{Short description|A psychedelic compound related to DMT}}
{{DISPLAYTITLE:5-Ethyl-DMT}}
{{Psychedelics}}


'''5-Ethyl-DMT''' is a [[psychedelic]] compound that belongs to the [[tryptamine]] class. It is structurally related to [[N,N-Dimethyltryptamine]] (DMT), a well-known psychedelic substance. The chemical structure of 5-Ethyl-DMT includes an ethyl group at the fifth position of the indole ring, distinguishing it from DMT.
== 5-Ethyl-DMT ==
[[File:5-Ethyl-DMT.svg|thumb|right|Chemical structure of 5-Ethyl-DMT]]
5-Ethyl-DMT, or 5-ethyl-N,N-dimethyltryptamine, is a [[psychedelic]] compound belonging to the [[tryptamine]] class. It is structurally related to other tryptamines such as [[DMT]] (N,N-dimethyltryptamine) and [[5-MeO-DMT]] (5-methoxy-N,N-dimethyltryptamine).


==Chemical Structure and Properties==
=== Chemical Structure ===
5-Ethyl-DMT is a derivative of DMT, with the chemical formula C14H20N2. The addition of an ethyl group at the 5-position of the indole ring alters its pharmacological properties compared to DMT. Like other tryptamines, it contains an indole ring structure, which is a common feature in many naturally occurring and synthetic psychedelics.
5-Ethyl-DMT is characterized by the presence of an ethyl group at the 5-position of the indole ring, distinguishing it from other tryptamines. The chemical formula is C14H20N2, and it has a molecular weight of 216.33 g/mol.


==Pharmacology==
=== Pharmacology ===
The pharmacological effects of 5-Ethyl-DMT are not well-documented, but it is presumed to act as a [[serotonin receptor]] agonist, similar to other tryptamines. This action is primarily at the [[5-HT2A receptor]], which is believed to be responsible for the psychedelic effects of these compounds. The specific binding affinity and activity of 5-Ethyl-DMT at various serotonin receptors have not been extensively studied.
As a tryptamine, 5-Ethyl-DMT is believed to act primarily as a [[serotonin receptor]] agonist, particularly at the [[5-HT2A receptor]], which is thought to be responsible for its psychedelic effects. However, detailed studies on its pharmacological profile are limited.


==Effects==
=== Effects ===
The subjective effects of 5-Ethyl-DMT are largely unknown due to limited research and anecdotal reports. However, it is expected to produce effects similar to other psychedelics, such as altered perception, visual hallucinations, and changes in thought processes. The duration and intensity of these effects can vary based on dosage, individual physiology, and environmental factors.
The effects of 5-Ethyl-DMT are not well-documented, but it is presumed to produce psychedelic experiences similar to other tryptamines, potentially including alterations in perception, mood, and cognition. The duration and intensity of these effects can vary based on dosage and individual factors.


==Legal Status==
=== Legal Status ===
The legal status of 5-Ethyl-DMT varies by country. In many jurisdictions, it may be considered a controlled substance due to its structural similarity to DMT and other tryptamines. It is important for individuals to be aware of the legal implications of possessing or using this compound in their respective regions.
The legal status of 5-Ethyl-DMT varies by country. In many jurisdictions, it may be considered a controlled substance due to its structural similarity to other regulated tryptamines.


==Synthesis==
== Related Compounds ==
The synthesis of 5-Ethyl-DMT involves the modification of the DMT molecule by introducing an ethyl group at the 5-position of the indole ring. This process requires advanced knowledge of organic chemistry and access to specific reagents and equipment. Due to the complexity and potential legal issues, synthesis is typically conducted in research settings.
* [[DMT]]
 
==Related Compounds==
* [[N,N-Dimethyltryptamine]] (DMT)
* [[5-MeO-DMT]]
* [[5-MeO-DMT]]
* [[4-AcO-DMT]]
* [[4-AcO-DMT]]
* [[Psilocybin]]
* [[Psilocybin]]


==Related Pages==
== See Also ==
* [[Psychedelic drug]]
* [[Psychedelic drug]]
* [[Serotonin receptor]]
* [[Tryptamine]]
* [[Tryptamine]]
* [[Serotonin receptor]]
* [[Hallucinogen]]


==Gallery==
== Related pages ==
<gallery>
* [[List of psychedelic tryptamines]]
File:5-Ethyl-DMT.svg|Chemical structure of 5-Ethyl-DMT
* [[Psychedelic experience]]
</gallery>


[[Category:Psychedelic tryptamines]]
[[Category:Tryptamines]]
[[Category:Serotonin receptor agonists]]
[[Category:Psychedelic drugs]]

Latest revision as of 03:47, 13 February 2025


5-Ethyl-DMT[edit]

Chemical structure of 5-Ethyl-DMT

5-Ethyl-DMT, or 5-ethyl-N,N-dimethyltryptamine, is a psychedelic compound belonging to the tryptamine class. It is structurally related to other tryptamines such as DMT (N,N-dimethyltryptamine) and 5-MeO-DMT (5-methoxy-N,N-dimethyltryptamine).

Chemical Structure[edit]

5-Ethyl-DMT is characterized by the presence of an ethyl group at the 5-position of the indole ring, distinguishing it from other tryptamines. The chemical formula is C14H20N2, and it has a molecular weight of 216.33 g/mol.

Pharmacology[edit]

As a tryptamine, 5-Ethyl-DMT is believed to act primarily as a serotonin receptor agonist, particularly at the 5-HT2A receptor, which is thought to be responsible for its psychedelic effects. However, detailed studies on its pharmacological profile are limited.

Effects[edit]

The effects of 5-Ethyl-DMT are not well-documented, but it is presumed to produce psychedelic experiences similar to other tryptamines, potentially including alterations in perception, mood, and cognition. The duration and intensity of these effects can vary based on dosage and individual factors.

Legal Status[edit]

The legal status of 5-Ethyl-DMT varies by country. In many jurisdictions, it may be considered a controlled substance due to its structural similarity to other regulated tryptamines.

Related Compounds[edit]

See Also[edit]

Related pages[edit]