5,6-Dibromo-DMT: Difference between revisions

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{{Short description|A brominated derivative of dimethyltryptamine}}
{{DISPLAYTITLE:5,6-Dibromo-DMT}}
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| ImageFile = 5,6-dibromo-DMT.svg
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| ImageAlt = Structural formula of 5,6-Dibromo-DMT
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'''5,6-Dibromo-DMT''' is a chemical compound that belongs to the class of [[tryptamines]], which are structurally related to the neurotransmitter [[serotonin]]. It is a derivative of [[dimethyltryptamine]] (DMT), a well-known psychedelic compound, with two bromine atoms substituted at the 5 and 6 positions of the indole ring.
== 5,6-Dibromo-DMT ==


==Chemical Structure==
[[File:5,6-dibromo-DMT.svg|thumb|right|Structural formula of 5,6-Dibromo-DMT]]
5,6-Dibromo-DMT is characterized by the presence of two bromine atoms attached to the indole ring of the DMT molecule. The chemical formula is C<sub>12</sub>H<sub>14</sub>Br<sub>2</sub>N<sub>2</sub>, and it has a molecular weight of 362.06 g/mol. The presence of bromine atoms significantly alters the electronic properties of the molecule compared to its parent compound, DMT.


==Synthesis==
'''5,6-Dibromo-DMT''' is a synthetic compound that belongs to the class of [[tryptamines]], which are a group of monoamine alkaloids. This compound is a derivative of [[dimethyltryptamine]] (DMT), a well-known psychedelic substance. The addition of bromine atoms at the 5 and 6 positions of the indole ring distinguishes 5,6-Dibromo-DMT from its parent compound.
The synthesis of 5,6-Dibromo-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 achieve selective substitution at the 5 and 6 positions of the indole ring.


==Pharmacology==
=== Chemical Structure ===
As a derivative of DMT, 5,6-Dibromo-DMT is expected to interact with the [[serotonin receptor|serotonin receptors]] in the brain. However, the specific pharmacological effects of 5,6-Dibromo-DMT have not been extensively studied. The addition of bromine atoms may influence the compound's affinity for these receptors and its overall psychoactive properties.


==Potential Uses==
5,6-Dibromo-DMT is characterized by the presence of two bromine atoms attached to the indole ring of the DMT molecule. The chemical formula for 5,6-Dibromo-DMT is C12H14Br2N2, and it has a molecular weight of 362.06 g/mol. The presence of bromine atoms significantly alters the electronic properties of the molecule compared to DMT.
While DMT is known for its psychedelic effects, the potential uses of 5,6-Dibromo-DMT remain largely unexplored. Research into similar compounds may provide insights into their potential applications in [[psychiatry]] or [[neuroscience]].


==Safety and Legal Status==
=== Synthesis ===
The safety profile of 5,6-Dibromo-DMT is not well-documented, and it is not widely used or studied. Its legal status may vary by jurisdiction, and it is important to consult local regulations regarding its use and possession.
 
The synthesis of 5,6-Dibromo-DMT involves the bromination of DMT. This process typically requires the use of a brominating agent, such as bromine or N-bromosuccinimide (NBS), under controlled conditions to selectively introduce bromine atoms at the 5 and 6 positions of the indole ring.
 
=== Pharmacology ===
 
The pharmacological properties of 5,6-Dibromo-DMT are not well-documented in scientific literature. However, as a derivative of DMT, it is likely to interact with [[serotonin receptors]], particularly the 5-HT2A receptor, which is known to mediate the psychedelic effects of tryptamines. The addition of bromine atoms may alter the binding affinity and activity of the compound at these receptors.
 
=== Potential Effects ===
 
While the specific effects of 5,6-Dibromo-DMT have not been extensively studied, it is hypothesized that it may produce psychedelic effects similar to those of DMT, such as altered perception, visual hallucinations, and changes in thought processes. However, the presence of bromine atoms could also result in unique effects or altered potency.
 
=== Safety and Toxicity ===
 
The safety and toxicity profile of 5,6-Dibromo-DMT is not well-established. As with many synthetic tryptamines, caution is advised due to the potential for unknown side effects and toxicological risks. Further research is needed to determine the safety of this compound in humans.
 
== Related Pages ==


==Related pages==
* [[Dimethyltryptamine]]
* [[Dimethyltryptamine]]
* [[Tryptamine]]
* [[Tryptamine]]
* [[Serotonin]]
* [[Psychedelic drug]]
* [[Psychedelic drug]]
* [[Serotonin receptor]]


[[Category:Tryptamines]]
[[Category:Tryptamines]]
[[Category:Psychedelic tryptamines]]
[[Category:Psychedelic tryptamines]]
[[Category:Organobromides]]

Latest revision as of 12:03, 15 February 2025


5,6-Dibromo-DMT[edit]

Structural formula of 5,6-Dibromo-DMT

5,6-Dibromo-DMT is a synthetic compound that belongs to the class of tryptamines, which are a group of monoamine alkaloids. This compound is a derivative of dimethyltryptamine (DMT), a well-known psychedelic substance. The addition of bromine atoms at the 5 and 6 positions of the indole ring distinguishes 5,6-Dibromo-DMT from its parent compound.

Chemical Structure[edit]

5,6-Dibromo-DMT is characterized by the presence of two bromine atoms attached to the indole ring of the DMT molecule. The chemical formula for 5,6-Dibromo-DMT is C12H14Br2N2, and it has a molecular weight of 362.06 g/mol. The presence of bromine atoms significantly alters the electronic properties of the molecule compared to DMT.

Synthesis[edit]

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

Pharmacology[edit]

The pharmacological properties of 5,6-Dibromo-DMT are not well-documented in scientific literature. However, as a derivative of DMT, it is likely to interact with serotonin receptors, particularly the 5-HT2A receptor, which is known to mediate the psychedelic effects of tryptamines. The addition of bromine atoms may alter the binding affinity and activity of the compound at these receptors.

Potential Effects[edit]

While the specific effects of 5,6-Dibromo-DMT have not been extensively studied, it is hypothesized that it may produce psychedelic effects similar to those of DMT, such as altered perception, visual hallucinations, and changes in thought processes. However, the presence of bromine atoms could also result in unique effects or altered potency.

Safety and Toxicity[edit]

The safety and toxicity profile of 5,6-Dibromo-DMT is not well-established. As with many synthetic tryptamines, caution is advised due to the potential for unknown side effects and toxicological risks. Further research is needed to determine the safety of this compound in humans.

Related Pages[edit]