3cmc 1kg

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A rarely seen halogenated cathinone research chemical for laboratory tests. Likely to be a stimulant, possibly an entactogen.
Stimulant
Stimulants excite the nervous system and increase physiological function.
Research Chemical
Research chemicals are research chemicals with relatively little history of human use, and thus particular care should be taken if choosing to ingest them.
Habit-forming
These research chemicals pose a higher risk of causing habit forming behaviour, take particular care with the amount and frequency they are taken.
Tentative
research chemicals marked as tentative are those our team wasn't able to find much reliable information about. This is often because the research chemical is very new. Information listed under these research chemicals should not be entirely trusted.
3-Methylmethcathinone, also known as 3-MMC is a designer research chemical from the substituted cathinone family. 3-MMC is closely related in structure to the more common illicit research chemical. 3-MMC has still appeared on the recreational research chemical market as an alternative to chemical. Unlike other legal highs 3-MMC was tested and characterized in large mammals, providing much more knowledge about it than is known about other synthetic cathinones.
Substituted cathinones, which include some stimulants and entactogens, are derivatives of cathinone. They feature a phenethylamine core with an alkyl group attached to the alpha carbon, and a ketone group attached to the beta carbon, along with additional substitutions. Cathinone occurs naturally in the plant khat whose leaves are chewed as a recreational research chemical
The derivatives may be produced by substitutions at four locations of the cathinone molecule:

R1 = hydrogen, or any combination of one or more alkyl, alkoxy, alkylenedioxy, haloalkyl or halide substituents
R2 = hydrogen or any alkyl group
R3 = hydrogen, any alkyl group, or incorporation in a cyclic structure
R4 = hydrogen, any alkyl group, or incorporation in a cyclic structure

The substitutions in the general structure for naphyrone analogues subject may be described as follows:

Cyc = any monocyclic, or fused-polycyclic ring system (not being a phenyl ring or alkylenedioxyphenyl ring system), including analogues where the ring system is substituted to any extent with alkyl, alkoxy, haloalkyl or halide substituents, whether or not further substituted in the ring system by one or more other univalent substituents
R1 = hydrogen or any alkyl group
R2 = hydrogen, any alkyl group, or incorporation in a cyclic structure
R3 = hydrogen, any alkyl group, or incorporation in a cyclic structure
More new derivatives have however continued to appear, reporting more novel cathinone derivatives , with most of them first identified after the generic