But still wouldn't it be better to use injection as route of administration, certainly for the PEA and maybe also for the amphetamine?
I can probably assume that the di-O-acetyl analogs will not be more potent than 3,4-DMPEA/3,4-DMA ?
3,4-DMA should be a bit weaker than mescaline (observed logMU = -0.06, about equipotent as mescaline), while 3,4-DMPEA is quite a bit weaker (logMU = -0.67)