3 MEC (3-Methylethcathinone) – Research Chemical Cathinone Compound

3-MEC , or 3-Ethylmethcathinone , is a synthetic stimulant of the cathinone class .
It is structurally related to 3-MMC and mephedrone , with an ethyl group at the 3-position of the phenyl ring. 3 mec

It is only examined in forensic and pharmacological laboratories and has no medical application .

Chemical and Pharmacological Background

Important information:

• IUPAC name: 1-(3-ethylphenyl)-2-(methylamino)propan-1-one

• Molecular formula: C12H17NO

• Molecular mass: ±191.27 g/mol

• Chemical class: Substituted cathinones

• Receptor action: Influences dopamine, serotonin and noradrenaline transporters.

The ethyl substitution affects receptor binding and metabolic stability, making it relevant for structure–activity studies .

Research purposes

3-MEC is being investigated for:

• Analytical detection: GC-MS, LC-MS, FTIR, and NMR.

• Forensic toxicology: identification in biological and seizure samples.

• Pharmacological research: study of neurotransmitter action and receptor activity.

• Public Health: Supporting early warning systems for stimulating NPS.

Safety and Legal Considerations

Safety:
Handle only by qualified researchers using personal protective equipment (PPE) .
Avoid contact and work in a well-ventilated area .

Legal status: 3-MEC is prohibited or regulated under psychoactive substances laws
in most countries . Use outside of research is punishable by law .

Frequently Asked Questions (FAQs)

1. What is 3-MEC being studied for?

For forensic, analytical and pharmacological research on cathinone compounds.

2. Is 3-MEC legal?

No, 3-MEC is regulated or banned in most countries .

3. How should 3-MEC be handled safely?

Only by professional researchers in controlled laboratories with proper safety protocols .

Conclusion

3-MEC (3-Ethylmethcathinone) is a key research topic in neuropharmacology and forensic chemistry .
It helps scientists understand how ethyl substitution affects the effects of stimulants. 1cp LSD