2-Methylphenethylamine
2-Methylphenethylamine (also known as 2MPEA) is a stimulant of the phenethylamine class. It is a positional isomer of amphetamine and is used in the manufacture of certain pharmaceuticals.
Chemistry[edit | edit source]
2-Methylphenethylamine is a phenethylamine, which is a group of organic compounds that include a phenyl ring directly attached to an amino group. It is a positional isomer of amphetamine, meaning it has the same molecular formula but a different arrangement of atoms.
Pharmacology[edit | edit source]
As a phenethylamine, 2-Methylphenethylamine has similar effects to other stimulants in this class. It increases levels of dopamine, norepinephrine, and serotonin in the brain, leading to increased arousal, alertness, and mood elevation.
Uses[edit | edit source]
2-Methylphenethylamine is used in the manufacture of certain pharmaceuticals. It is also used as a starting material in the synthesis of various psychoactive substances.
Safety[edit | edit source]
The safety profile of 2-Methylphenethylamine is not well-studied. As a stimulant, it may have potential for abuse and addiction. It may also have side effects similar to other stimulants, such as increased heart rate, blood pressure, and risk of stroke.
See also[edit | edit source]
2-Methylphenethylamine Resources | ||
---|---|---|
|
|
Translate to: East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
Urdu,
বাংলা,
తెలుగు,
தமிழ்,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
European
español,
Deutsch,
français,
русский,
português do Brasil,
Italian,
polski
Navigation: Wellness - Encyclopedia - Health topics - Disease Index - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes
Search WikiMD
Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro) available.
Advertise on WikiMD
WikiMD is not a substitute for professional medical advice. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.Contributors: Prab R. Tumpati, MD