3-MEC
€15.00 – €80.00Price range: €15.00 through €80.00
3 MEC (3-Methylethcathinone) – Research Chemical Cathinone Compound
3-MEC, or 3-Ethylmethcathinone, is a synthetic stimulant from the cathinone class.
It is structurally related to 3-MMC and mephedrone, immediately ethyl group at the 3-position of the phenyl ring. 3 mec
It is only investigated within 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 function: Affects dopamine, serotonin, and noradrenaline transporters.
The ethyl substitution influences receptor binding and metabolic stability, making it relevant for structure–activity research.
Research purposes
3-MEC is being investigated for:
Analytical detection: GC-MS, LC-MS, FTIR, and NMR.
Forensic toxicology: identification in biological and seized samples.
Pharmacological research: study of neurotransmitter function and receptor activity.
Public health: support of 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 ventilated environment.
Legal status:
3-MEC is available in most countries prohibited or regulated under the psychoactive substances legislation.
Use outside of research purposes is punishable.
Frequently Asked Questions (FAQ's)
1. What is 3-MEC being studied for?
For forensic, analytical and pharmacological research to cathinone compounds.
2. Is 3-MEC legal?
No, 3-MEC is available in most countries regulated or prohibited.
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 an important research subject within the neuropharmacology and forensic chemistry.
It helps scientists understand how ethyl substitution influences the effect of stimulants. 1cp lsd
3 MEC (3-Methylethcathinone) – Research Chemical Cathinone Compound
3-MEC, or 3-Ethylmethcathinone, is a synthetic stimulant from the cathinone class.
It is structurally related to 3-MMC and mephedrone, immediately ethyl group at the 3-position of the phenyl ring. 3 mec
It is only investigated within 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 function: Affects dopamine, serotonin, and noradrenaline transporters.
The ethyl substitution influences receptor binding and metabolic stability, making it relevant for structure–activity research.
Research purposes
3-MEC is being investigated for:
Analytical detection: GC-MS, LC-MS, FTIR, and NMR.
Forensic toxicology: identification in biological and seized samples.
Pharmacological research: study of neurotransmitter function and receptor activity.
Public health: support of 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 ventilated environment.
Legal status:
3-MEC is available in most countries prohibited or regulated under the psychoactive substances legislation.
Use outside of research purposes is punishable.
Frequently Asked Questions (FAQ's)
1. What is 3-MEC being studied for?
For forensic, analytical and pharmacological research to cathinone compounds.
2. Is 3-MEC legal?
No, 3-MEC is available in most countries regulated or prohibited.
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 an important research subject within the neuropharmacology and forensic chemistry.
It helps scientists understand how ethyl substitution influences the effect of stimulants. 1cp lsd
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