I tried 3-MeO-PCE tonight and it was amazing. Will give a proper report in the morning. It felt so fucking clean. Wasn't too stimulating at all! Really, really good time.
Edit: I'm a bit late. But here are more detailed notes.
A few days ago, I finally got to try 3-meo-pce. I started off by dissolving 10 - 15 mg in 1 mL of warm water, and squirting it up my butt. I did about 75% of it, then 15 - 30 minutes later, refilled the syringe and did the rest. I am not sure how much of this dose I absorbed. I definitely got some, and I did have a bowel movement beforehand. However, I've been using kratom daily for a while now. So I might still have been backed up. For what it's worth, there was no fecal matter on the syringe after I removed it.
And so began the waiting game. I had a few first alert type feelings, but nothing too significant. Over the next 4 hours, I proceeded to do small bumps of out 2.5mg space no less than 30 minutes apart. I eventually got to a point where I was definitely feeling it, and decided not to do any more redoses.
Seems like there is no way to avoid the long come up. Is 3-MeO-PCE a prodrug for PCE?
What impressed me most about this compound was just how lucid it left me. I felt very zen, content, happy with things as they were. And I was definitely dissociated, but there was virtually none of the mindfuck I've come to associate with dissociatives. It was a very cerebral high. I could think clearly, although articulating those thoughts was a little bit more difficult than normal.
I believe I took 20 - 30 mg in total. Next time, I'd like to try 20 mg in a single dose, instead of repeated small doses.
I did not find it to be particularly stimulating. Certainly not compared to ephenidine, which I now consider to be "cracked out." My previous impression of that chemical were merely a function of my hazy memory of how actual ACH's feel.
Like I said, I've been taking Kratom everyday. The 3-MeO-PCE seemed to lessen the withdrawal. I'm not saying it has opioid receptor affinity or anything. I suspect that the anasthetic properties may dull one to the sensations of withdrawal, just as they would for any other pain.
When I think of how it felt, the words that continue to surface are along the lines of: serene, clear, clean, zen, calm, content.
There was no intensity, no existential anxiety. I just felt fucking awesome.
I could see how this sharpened thinking may lead some to consider this drug a stimulant. I didn't feel any physical stimulation (no noticabley increased heartrate or jaw tension--however, I did experience some jaw tension during the come down). However, I did not measure heart rate or blood pressure, so I might be wrong about that.
It felt vaguely psychedelic in a way. Like, if you were to isolate just one aspect of an LSD headspace, this drug seemed to replicate that, but without any of the other hallmarks of a tryptamine. I would not be surprised to find it had significant affinity for serotonin receptors.
While the peak passed me by because I was too busy analyzing myself, the period just after the peak (so far from baseline) was spent watching Gantz:0, which is a CGI movie remake of an anime I was somewhat infatuated with in highschool. Dissociatives almost always have either a nostalgic or futuristic bent to them. They make me feel like I am living in a science fiction epic. This choice of film played to both aspects of the high. I was nostalgic for the days gone, when I watched the original Gantz in highschool. And the SF aesthetic of the film appealed to me as well.
After Gantz, I watched the first episode of 3%. Again, the science fiction aesthetic appealed to me very much while I was in this state.
I wish I had more to say to y'all. The effects of this drug are somehow subtle and brazen at the same time. It is very hard to explain.
One piece of advice I would offer: Do not try to hole on this. It felt more like a "ceiling" than a hole to me. I fear that if I just kept on redosing, I would have found myself in a manic state.
