Morninggloryseed
Bluelight Crew
I think I see where you are going wioth it. I thought you meant "4-O-DMT" stays that way if reacted. I don't think it can exist without either an H, or something like a Ca or as the Acetyl ester. I'd bet 5-AcO-DMT would be active.
Anadenanthera said:It’s a well known fact that phenolic compounds behave like this. You do know about phenol right? Bufotenin is based on phenol. If you react calcium hydroxide with phenol, you get calcium phenoxide. It loses the H and forms a salt with calcium. The same thing happens with morphine, psilocin, and bufotenin is no exception to this rule. Look up phenoxide and phenol, and you'll see what I'm talking about.
How is it possible for this rule not to apply with bufotenine when it clearly applies to phenol, morphine and psilocin? Can someone please explain how bufotenine could be the one exception to this rule?