e1evene1even
Bluelighter
- Joined
- May 11, 2006
- Messages
- 1,504
O-PCE is likely in my top 5 drugs of all-time despite having only used relatively low doses (~10-14mg + a similar redose with a decent disso tolerance). I have a close friend who feels the same.
Interesting anecdote, when I met very well-known psychonaut/chemist last year (to remain unnamed for privacy), it was the only thing I had to offer, and while he didn't partake due to having an early flight he also expressed it being his current favorite drug to my surprise.
After finding a small stash of MXE recently, I think I actually prefer O-PCE, at least in lower doses. It feels more functional and clear-headed. But after a year of regular K issue however, I'm unable to compare things at baseline.
Also after reading some of the speculation on O-PCE being potentially risky with regular use do to hypothetical antibacterial/antimicrobial properties, I'm a bit more risk-averse with it. If anyone has a definitive rebuttal to these claims, I'd love to know (probably discussed to death here, but I've been out of the loop). The study published in HK showing a large cluster of adverse effects is another reason I want to be cautious and not assume it has same relative safety as MXE.
www.ncbi.nlm.nih.gov
At that this point it seems to be a gone for now, so I've been dabbling with 3-MeO-PCE. My initial impression is that it lacks much of the magic of O-PCE, and has less of the perfect hypo-mania (in contrast to the more forceful and less forgiving raw power of 3-MeO-PCP), it's still quite well-rounded, and may be the best thing available (for me at least at this point).
Based on the receptor affinity studies, 3-MeO-PCE/O-PCE seem to share MXE's far more complex pharmacology compared ketamine which make them 'deeper' in many respects, but with more room for unexpected interactions and risks when the tolerance to the NMDA effects builds rapidly, while the secondary effects can be cumulative with re-dosing...
(Btw Xorkoth, I wrote you a long PM, but it got lost before I sent it
I'll try again soon)
Interesting anecdote, when I met very well-known psychonaut/chemist last year (to remain unnamed for privacy), it was the only thing I had to offer, and while he didn't partake due to having an early flight he also expressed it being his current favorite drug to my surprise.
After finding a small stash of MXE recently, I think I actually prefer O-PCE, at least in lower doses. It feels more functional and clear-headed. But after a year of regular K issue however, I'm unable to compare things at baseline.
Also after reading some of the speculation on O-PCE being potentially risky with regular use do to hypothetical antibacterial/antimicrobial properties, I'm a bit more risk-averse with it. If anyone has a definitive rebuttal to these claims, I'd love to know (probably discussed to death here, but I've been out of the loop). The study published in HK showing a large cluster of adverse effects is another reason I want to be cautious and not assume it has same relative safety as MXE.

Cluster of acute poisonings associated with an emerging ketamine analogue, 2-oxo-PCE - PubMed
Ketamine and phencyclidine are well-known drugs of abuse of the arylcyclohexylamine class, the backbone of which is used for the synthesis of new psychoactive substances (NPS). In October 2017, a cluster of acute intoxications was encountered where patients presented with ketamine-like...

At that this point it seems to be a gone for now, so I've been dabbling with 3-MeO-PCE. My initial impression is that it lacks much of the magic of O-PCE, and has less of the perfect hypo-mania (in contrast to the more forceful and less forgiving raw power of 3-MeO-PCP), it's still quite well-rounded, and may be the best thing available (for me at least at this point).
Based on the receptor affinity studies, 3-MeO-PCE/O-PCE seem to share MXE's far more complex pharmacology compared ketamine which make them 'deeper' in many respects, but with more room for unexpected interactions and risks when the tolerance to the NMDA effects builds rapidly, while the secondary effects can be cumulative with re-dosing...
(Btw Xorkoth, I wrote you a long PM, but it got lost before I sent it
