5,6-diBr-DMT

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5,6-diBr-DMT (5,6-dibromo-N,N-dimethyltryptamine) is a synthetic compound belonging to the tryptamine class. It is a derivative of DMT (N,N-dimethyltryptamine), a naturally occurring psychedelic substance. The addition of bromine atoms at the 5 and 6 positions of the indole ring distinguishes 5,6-diBr-DMT from its parent compound.

Chemical Structure and Properties[edit | edit source]

5,6-diBr-DMT is characterized by the presence of two bromine atoms attached to the indole ring of the tryptamine backbone. The chemical formula for 5,6-diBr-DMT is C12H14Br2N2, and it has a molecular weight of 346.06 g/mol.

The structure of 5,6-diBr-DMT can be represented as follows:

  • Indole ring: A bicyclic structure consisting of a benzene ring fused to a pyrrole ring.
  • Bromine substituents: Two bromine atoms are attached at the 5 and 6 positions of the indole ring.
  • Dimethylamino group: A dimethylamino group is attached to the ethyl side chain at the 3-position of the indole ring.

Synthesis[edit | edit source]

The synthesis of 5,6-diBr-DMT involves the bromination of DMT. This process typically requires the use of brominating agents such as bromine or N-bromosuccinimide (NBS) under controlled conditions to selectively introduce bromine atoms at the desired positions on the indole ring.

Pharmacology[edit | edit source]

The pharmacological properties of 5,6-diBr-DMT are not well-documented in scientific literature. However, as a derivative of DMT, it is likely to interact with the serotonin receptors in the brain, particularly the 5-HT2A receptor, which is known to mediate the effects of many psychedelic compounds.

Potential Effects[edit | edit source]

Due to the lack of comprehensive studies, the psychoactive effects of 5,6-diBr-DMT remain speculative. It is hypothesized that, like other tryptamines, it may produce altered states of consciousness, visual and auditory hallucinations, and changes in perception and mood.

Legal Status[edit | edit source]

The legal status of 5,6-diBr-DMT varies by country. In many jurisdictions, it may be considered a controlled substance due to its structural similarity to DMT and other tryptamines, which are often regulated under drug laws.

Research and Applications[edit | edit source]

Research on 5,6-diBr-DMT is limited, and its potential applications in medicine or other fields have not been extensively explored. It may be of interest in the study of structure-activity relationships (SAR) among tryptamines and their effects on the central nervous system.

Also see[edit | edit source]



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