4-methyl-2,5-dimethoxyamphetamine

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4-Methyl-2,5-dimethoxyamphetamine (4-Methyl-2,5-DMA), is a psychoactive drug and a substituted amphetamine. It is part of a class of compounds known as phenethylamines, sharing core structural similarities with amphetamines and hallucinogens. This compound is known for its psychedelic and stimulant effects, which are attributed to its action on the serotonin, dopamine, and norepinephrine receptors in the brain.

Chemistry[edit | edit source]

4-Methyl-2,5-dimethoxyamphetamine belongs to the substituted amphetamines class, which is characterized by the substitution of the amphetamine core structure with various alkyl groups and methoxy (-OCH3) groups. The chemical formula for 4-Methyl-2,5-DMA is C11H17NO2, indicating the presence of 11 carbon atoms, 17 hydrogen atoms, one nitrogen atom, and two oxygen atoms in its structure. The modifications at the 2 and 5 positions of the benzene ring with methoxy groups, and the addition of a methyl group at the 4 position, distinguish it from other amphetamines and contribute to its unique pharmacological properties.

Pharmacology[edit | edit source]

The pharmacological action of 4-Methyl-2,5-DMA is primarily due to its interaction with the serotonin receptors in the brain, particularly the 5-HT2A receptor, which is known to play a key role in the effects of many psychedelic drugs. It may also affect dopamine and norepinephrine receptors, contributing to its stimulant effects. However, detailed studies on its pharmacodynamics are limited, and much of what is known comes from anecdotal reports and comparisons with closely related compounds.

Effects[edit | edit source]

Users of 4-Methyl-2,5-DMA report a range of psychedelic and stimulant effects, including altered states of consciousness, enhanced sensory perception, increased energy, and euphoria. The intensity and duration of these effects can vary based on the dose, route of administration, and individual user characteristics. As with many psychoactive substances, the use of 4-Methyl-2,5-DMA can also lead to negative side effects such as anxiety, paranoia, and physiological stress reactions.

Legal Status[edit | edit source]

The legal status of 4-Methyl-2,5-DMA varies by country, with many jurisdictions classifying it as a controlled substance due to its potential for abuse and the lack of recognized medical use. In countries where it is controlled, possession, manufacture, and distribution of 4-Methyl-2,5-DMA may be subject to criminal penalties.

Research[edit | edit source]

Research on 4-Methyl-2,5-DMA has been limited, with most studies focusing on its chemistry and pharmacology in the context of understanding the broader class of substituted amphetamines. There is interest in exploring its potential therapeutic applications, particularly in the treatment of psychiatric disorders, but such research is in the early stages and faces significant regulatory and ethical challenges.

See Also[edit | edit source]


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