It must not be too difficult because the most recent data shows PT hydrogenation as the most commonly used reduction when looking at MDMA analyzed in Aus a few years back.
Palladium catalyst is very easy to recover I’m gonna assume platinum isn’t much different in recovery.
So guys I might have an interesting clue... A sample of expected “2cb” was analyzed that was purchased in Mexico. It contained no 2cb but one of the ingredients was MDMA as well as 5x the amount of that MDMA of n-acetyl-mdma.
This impurity has never been picked up by EData but has been an impurity that’s been around for awhile based on some literature I’ve found. I’ll continue to dig to see what I find.
I’m shocked at the fact there is 5x the amount, that means that MDMA before being put into this mixed product was essentially mostly n-acetyl-mdma. I wanna know what synthesis route this originated from.
I do know GAA is used in the PT hydrogenation, would this maybe be the cause of our impurity. I wonder if this may be potentially our culprit impurity.
-GC