5,6-diBr-DMT
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
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
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
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
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
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
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
| Tryptamines |
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Contributors: Prab R. Tumpati, MD