DMXE Pellets 40mg

Ensure to store the DMXE powder and pellets in a dry and cool place for maximum shelf-life. When handling research chemicals ensure to always take the proper precautions in the laboratory like wiping down surfaces and wearing gloves, a mask & protective clothing.

The compounds in the arylcyclohexylamine group can be qualified as dissociative anesthetics with hallucinogenic properties. There are many different compounds in this category, the first of which were synthesized more than a century ago. PCA was first recorded to be synthesized in 1907.

The effects range from being fairly stimulating to relatively sedating. DMXE is relatively new and has not been researched very much. Research outcomes so far suggest that the substance is a little bit less potent than MXE while sharing a number of similarities in terms of duration and research effects.

One of the reasons that there is so much variety among the arylcyclohexylamine is because of the way that hydrogen atoms in the structure can be substituted for other functional groups. This can produce a range of chemicals with wildly varying effects.

DMXE is structurally quite similar to MXE, however, the methoxy group is replaced with methyl (meaning that the oxygen has been replaced, hence giving rise to the deoxy in the substance’s name).

Research is still young in regards to DMXE. However, some researchers speculate that its potency can be determined by gauging the chemical process that leads to its creation.

When you add the ketone to 3-MeO-PCE, another popular research chemical arylcyclohexylamine, NMDAr potency is reduced by about 8.5 and sertraline affinity is reduced by about 3.5x.

Comparing these numbers to the affinities of MXE and the relative molecular changes, one could expect that it would be about 1.4x less potent as an NMDAr antagonist than MXE, and yet 1.2x more potent at the sertraline receptor site.

DMXE cannot be O-demethylated, however, which could lead to a longer onset and duration despite the decreased potency.