Do you have any preferences among these base tryptamines Kaleida? It seems like you've sampled the tryptamines pretty widely
I have indeed sampled my fair share of tryptamines, but I actually don't have all that much experience with all the base tryptamine yet. I do, however, own all of those that I named, as well as DiPT, and will be trying all of them within the upcoming months... so I should have a better answer for that soon.
So far, the base tryptamines I
have tried are DMT, MET, MiPT, DiPT, and DALT. Of them, MiPT was absolutely my favorite.... Nothing else even comes close. I could rave about it here, but my
trip report is what would really do it justice, I try not to recommend my own writings too much but I'd definitely say you should check it out if you're interested! Of the rest, DMT has given me by far the strongest effect, but MET, which I've only briefly explored, feels extremely similar but much easier to handle so far, like it's almost the same trip but drawn out a bit more so the initial rush is significantly calmer and the afterglow is longer-lasting, and I also find it much more euphorically stimulating than DMT's afterglow, much like a 4-HO-MET trip versus mushrooms. The visuals were also just a bit more hedonistic than DMT's, they have that stereotypical "LSD-like" feeling that again also applies to this tail change for the 4-substituted tryptamines. Notably, I have also given a family member a breakthrough on it, and they've never had a DMT breakthrough, but they were a big acidhead in the '60s. They claimed it to be one of the best psychedelics they've tried so far, and remained completely calm and mostly capable of regular conversation through it, despite the fact that they were able to go in and out of the alternate worlds simply by closing and opening their eyes, respectively, for an entire hour, and actually simply chose to call it quits and go to bed happily before actually coming down, they were actually just that satisfied by it already by then. So, I definitely think that sounds like a pretty promising one too!
Also, of course, DiPT is remarkable in its own way, but as a basic psychedelic it's not really something that has overly impressed me yet. The audio distortions, however, are absolutely astounding, and unlike anything any other psychedelic, except those few also containing isopropyl tails, could ever do.
Long-lasting salvia? Sounds like... a probable nightmare.
Heh heh, to each their own.
I love salvia personally, and think that one of its main problems is its short duration. And, for what it's worth, I also tend to think that salvia suffers from "comeup syndrome", which I just now made up. The same is true of smoked DMT.... When comparing it to oral psychedelics, it seems clear to me that the DMT trip is mainly an extremely strong comeup, one so powerful that it makes you totally delirious, but then the trip fades before the "regular" trip starts, which we associate most of the oral psychedelic experience with. So, I feel that salvia is the same, and that if it were extended it could likely produce more of a plateau stage as well.... This is, at the very least, supported by my experiences smoking it several times back to back; the first smoke was exactly like any other single time salvia trip, but the subsequent smokes were completely different, not dissociating at all but instead very grounded in my body, surprisingly euphoric, and with beautiful open eye visuals similar to both psychedelics and deliriants, whereas the first hit for me is almost always just closed eye visuals of the kind that typically accompany ego loss-type experiences, which again is just like the comeup/peak of a psychedelic to me more so than the plateau. So, I will definitely reserve my judgement of a long-lasting salvia analogue until I've actually tried one personally....
"Salvinorin B methoxymethyl ether". Claimed to be approximately 5 times the duration and potency of salvinorin A.
That one I am quite interested in as well.
The ethoxymethyl version also sounds quite interesting to me from the reports. However, in this case I was referring to
this study, which just came out a few months ago. It seems to me like the rigid structures they developed here could make for significantly greater metabolic stability than even the Salvinorin B methoxymethyl and ethyoxyethyl ethers, which from the reports honestly sound like they still don't last that much longer than salvinorin A does.