5-MeO-α,N,N-TMT

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5-MeO-α,N,N-TMT (5-Methoxy-α,N,N-trimethyltryptamine) is a synthetic compound belonging to the class of tryptamines, which are structurally related to the neurotransmitter serotonin. This compound is of interest in the field of psychopharmacology due to its structural similarity to other psychoactive tryptamines.

Chemical Structure and Properties[edit | edit source]

5-MeO-α,N,N-TMT is a derivative of tryptamine, characterized by the presence of a methoxy group at the 5-position of the indole ring, and a trimethyl substitution at the α and N positions. The chemical formula for 5-MeO-α,N,N-TMT is C14H20N2O, and its molecular weight is 232.32 g/mol.

Synthesis[edit | edit source]

The synthesis of 5-MeO-α,N,N-TMT typically involves the methylation of 5-methoxytryptamine. This process can be achieved through various chemical reactions, including the use of methylating agents such as methyl iodide in the presence of a base.

Pharmacology[edit | edit source]

The pharmacological profile of 5-MeO-α,N,N-TMT is not well-documented, but it is presumed to interact with serotonin receptors in the brain, similar to other tryptamines. The compound's psychoactive effects, if any, have not been extensively studied in humans or animals.

Potential Effects[edit | edit source]

Due to its structural similarity to other 5-methoxytryptamines, 5-MeO-α,N,N-TMT may exhibit hallucinogenic properties. However, there is limited empirical data on its effects, safety, and potential therapeutic applications.

Legal Status[edit | edit source]

The legal status of 5-MeO-α,N,N-TMT varies by country. In many jurisdictions, it may be considered a controlled substance due to its potential for psychoactive effects and structural similarity to other regulated tryptamines.

Research and Applications[edit | edit source]

Research on 5-MeO-α,N,N-TMT is limited, and it is primarily of interest to researchers studying the structure-activity relationships of tryptamines. Its potential applications in medicine or therapy remain speculative at this stage.

Also see[edit | edit source]



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