2C-T-28: Difference between revisions

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{{Short description|A psychedelic phenethylamine of the 2C family}}
== 2C-T-28 ==
{{Drugbox
| verifiedfields = changed
| verifiedrevid = 477318123
| IUPAC_name = 2-[4-(Isopropylthio)-2,5-dimethoxyphenyl]ethanamine
| image = 2CT28_structure.png
}}


'''2C-T-28''' is a psychedelic phenethylamine of the [[2C (psychedelics)|2C family]]. It is a synthetic compound that was first synthesized by [[Alexander Shulgin]].
[[File:2CT28_structure.png|thumb|right|Chemical structure of 2C-T-28]]


==Chemical structure==
'''2C-T-28''' is a synthetic psychedelic compound belonging to the [[2C family]] of [[phenethylamines]]. It is known for its psychoactive properties and is structurally related to other compounds in the 2C-T series, such as [[2C-T-7]] and [[2C-T-2]].
2C-T-28 is chemically related to other members of the 2C family, such as [[2C-T-7]] and [[2C-T-2]]. Its full chemical name is 2-[4-(Isopropylthio)-2,5-dimethoxyphenyl]ethanamine. The structure consists of a phenethylamine backbone with methoxy groups at the 2 and 5 positions and an isopropylthio group at the 4 position.


==Pharmacology==
=== Chemical Structure ===
The pharmacological properties of 2C-T-28 are not well-documented, but it is believed to act as a [[serotonin receptor]] agonist, similar to other 2C compounds. This action is thought to be responsible for its psychedelic effects.


==Effects==
2C-T-28 is chemically classified as a [[phenethylamine]], which is a class of compounds characterized by a phenyl ring bound to an amino group through an ethyl chain. The chemical structure of 2C-T-28 includes a thioether group, which is a sulfur atom bonded to two carbon atoms, and a methoxy group attached to the phenyl ring. This structure is similar to other compounds in the 2C-T series, which are known for their [[psychedelic]] effects.
The effects of 2C-T-28 are not well-studied, but it is presumed to produce effects similar to other 2C compounds, which may include altered perception, mood, and cognition. The duration and intensity of these effects can vary based on dosage and individual sensitivity.


==Legal status==
=== Pharmacology ===
The legal status of 2C-T-28 varies by country. In some jurisdictions, it may be classified as a controlled substance due to its structural similarity to other regulated 2C compounds.


==Synthesis==
The pharmacological effects of 2C-T-28 are not well-documented, but it is believed to act as a [[serotonin receptor]] agonist, similar to other 2C compounds. This action on serotonin receptors is thought to be responsible for its psychedelic effects, which may include altered perception, mood changes, and visual hallucinations.
The synthesis of 2C-T-28 involves the introduction of an isopropylthio group to the phenethylamine structure. This process requires specialized knowledge in organic chemistry and access to specific reagents and equipment.


==Safety and toxicity==
=== Effects ===
There is limited information on the safety and toxicity of 2C-T-28. As with many research chemicals, the lack of comprehensive studies means that potential risks are not fully understood. Users should exercise caution and be aware of the potential for adverse effects.
 
The effects of 2C-T-28 are reported to be similar to those of other 2C-T compounds, with users experiencing a range of psychedelic effects. These may include:
 
* Enhanced sensory perception
* Visual and auditory hallucinations
* Altered sense of time
* Emotional and cognitive changes
 
The duration and intensity of these effects can vary depending on the dose and individual sensitivity.
 
=== Legal Status ===
 
The legal status of 2C-T-28 varies by country. In some jurisdictions, it may be classified as a controlled substance due to its structural similarity to other regulated 2C compounds. Users should be aware of the legal implications of possessing or using 2C-T-28 in their region.
 
== Related Pages ==


==Related pages==
* [[2C-T-2]]
* [[2C-T-2]]
* [[2C-T-7]]
* [[2C-T-7]]
* [[2C (psychedelics)]]
* [[2C family]]
* [[Alexander Shulgin]]
* [[Phenethylamine]]
* [[Psychedelic]]


[[Category:Psychedelic phenethylamines]]
[[Category:Psychedelic phenethylamines]]
[[Category:2C (psychedelics)]]
[[Category:2C (psychedelics)]]

Latest revision as of 04:03, 13 February 2025

2C-T-28[edit]

Chemical structure of 2C-T-28

2C-T-28 is a synthetic psychedelic compound belonging to the 2C family of phenethylamines. It is known for its psychoactive properties and is structurally related to other compounds in the 2C-T series, such as 2C-T-7 and 2C-T-2.

Chemical Structure[edit]

2C-T-28 is chemically classified as a phenethylamine, which is a class of compounds characterized by a phenyl ring bound to an amino group through an ethyl chain. The chemical structure of 2C-T-28 includes a thioether group, which is a sulfur atom bonded to two carbon atoms, and a methoxy group attached to the phenyl ring. This structure is similar to other compounds in the 2C-T series, which are known for their psychedelic effects.

Pharmacology[edit]

The pharmacological effects of 2C-T-28 are not well-documented, but it is believed to act as a serotonin receptor agonist, similar to other 2C compounds. This action on serotonin receptors is thought to be responsible for its psychedelic effects, which may include altered perception, mood changes, and visual hallucinations.

Effects[edit]

The effects of 2C-T-28 are reported to be similar to those of other 2C-T compounds, with users experiencing a range of psychedelic effects. These may include:

  • Enhanced sensory perception
  • Visual and auditory hallucinations
  • Altered sense of time
  • Emotional and cognitive changes

The duration and intensity of these effects can vary depending on the dose and individual sensitivity.

Legal Status[edit]

The legal status of 2C-T-28 varies by country. In some jurisdictions, it may be classified as a controlled substance due to its structural similarity to other regulated 2C compounds. Users should be aware of the legal implications of possessing or using 2C-T-28 in their region.

Related Pages[edit]