5-Methoxytryptamine (5-MT)

5-Methoxytryptamine (5-MT), also known as mexamine, is a tryptamine derivative
closely related to the neurotransmitters serotonin and melatonin. 5-MT has been
shown to occur naturally in the body in low levels. It is biosynthesized via
the deacetylation of melatonin in the pineal gland. The protective effect of 5-
methoxytryptamine (a metabolite of melatonin) in human keratinocytes against
ultraviolet B (UVB) radiation was studied. Melatonin and its metabolites
ameliorate ultraviolet B-induced damage in human epidermal keratinocytes.
In terms of application, 5-Methoxytryptamine exhibits several significant
properties. One of its primary areas of interest is its role in neuroscience
and psychiatry. It is known to interact with serotonin receptors in the brain,
particularly the 5-HT2A receptor, which is associated with mood regulation and
perception. In addition to its neuropharmacological effects, 5-
Methoxytryptamine has been investigated for its role in psychotropic research.
It is often used as a research tool to understand the mechanisms of
psychoactive substances and their interactions with neurotransmitter systems.
Moreover, 5-Methoxytryptamine has been explored in the context of entheogenic
research, which examines the use of psychoactive substances in spiritual or
religious practices. Its psychoactive effects and interactions with serotonin
receptors contribute to its interest in studies on altered states of
consciousness and their therapeutic applications. The chemical synthesis of 5-
Methoxytryptamine typically involves the introduction of a methoxy group into
the tryptamine structure. This process is often achieved through a series of
chemical reactions that modify the indole ring of tryptamine. Characterization
of the synthesized compound is performed using analytical techniques such as
high-performance liquid chromatography (HPLC) and mass spectrometry (MS), which
ensure the purity and identity of the final product. In summary, 5-
Methoxytryptamine is a chemically intriguing compound with applications
spanning neuropharmacology, psychiatry, and psychotropic research. Its
interaction with serotonin receptors and potential therapeutic effects make it
a subject of ongoing interest in the study of neurotransmitter systems and
psychoactive substances.
Brand: Soarwin
CAS No.: 608-07-1
EC Number: 210-153-7
Molecular Formula: C11H14N2O
Density: 1.0815 (rough estimate)
Melting point: 121-123°C(lit.)
Boiling point: 325.75°C(Predicted)

Minimum Order: 1 kilograms