Actually, my understanding is that n-methyl-tryptamine, the monomethylated semi-honey, is the main physiologically undesirable constituent, not only in Phalaris, but also in the Australian acacia wattles. This is awkward, because it is really hard to separate in an extemporaneous extraction. Heck, it ain't really all that easy to separate by chromatography, and forget fractional distillation.
There are several chemical methods of precipitating secondary amines in the presence of tertiary amines, and what they all have in common is that they have all, each and every one of them, slipped my mind at this very moment when I wanted to spout them out! Anyway, this would bee a very handy piece of knowledge to disseminate, especially to the Ozbees among us. When I look it up, I'll post it. The scheme is, to pull out the monomethylamines chemically, take them aside and stuff the missing methyl in. Then they could be combined with the other extractive, DMT and 5-MeO-DMT, to double the yield. The 5-MeO reportedly isn't too bad a trip, just not super-psychedelic like DMT is. The n-monomethyl, though, is no fun, not a trip, and causes bad side effects. I'll get back when I've refreshed my amine sep principles.
Half-a-Pint
Half a pint's a half a pound, a half the world around, around.