I swear up and down that the construction changed pre-2026
This is something that's caught my eye recently, tons of folks have been going off about how there was a distinct shift in the subjective qualities of 7-OH around the beginning of 2026 or the end of 2025, and it also correlated to every kratom chemist I know beginning to ignore the importance of inert atmosphere when oxidizing mitragynine. The general hunch is that there's an unexpected synthetic byproduct of oxidizing in these more fast-and-loose conditions, but without mass spec magic to stratify really closely related compounds from one another, it'll be tough to tell. Mitragyna alks aren't going anywhere thankfully.
I know a shop that goes around buying any shop's excess unsold material. One week, I had three different Opia 30mg singles packs. One had no expiration dates & no tear slit (very strong, stronger than the other two). One had an expiration date and tear slit (weaker than the 1st). The 3rd, had an expiration date & tear slit (and blew ass). As I remember when the Opia Ultra 60mg came out and they were strong, then all of a sudden they strength fell out the bottom.
That shop sounds sketchy as fuck, is there a reason you never just purchased crystal 7-OH? I'd expect that working with it would be far cheaper, easier to control and keep logs of, etc.
Speaking of which, did you have any of these samples analyzed? If so please share what was found.
I know I have a advanced high opioid tolerance but they weren't pulling that trick on me. From what I read from a testing lab, the older batches had two different types of 7-OH and the newer ones are not showing that compound.
All Fentanyl does is keep me up all night with no opioid feeling.
I'm assuming we're talking street fent, you ever have any tested through a testing facility? I'd love to know which fentalogs are most prone to stimulation, the concept of isolating the stimulation from opioid-dominant scaffolds is super neat. I can use oxycodone like a stimulant, I'm assuming you're similar in that regard?
I wonder if the "second type" of 7-OH you're referring to is related to the difference in using inert conditions, idk just a hunch. The idea though that there's some sort of conspiracy out there to fool somebody who already has an established tolerance is sort of silly to support, were you doing blind trials on people who don't use frequently? That's the only way I've been able to gain any accuracy/precision whatsoever surrounding drug responses personally, if I tested everything on myself I'd think the most ideal dose of LSD is ~20 tabs for example. Brains all vary in exceptionally weird ways, a large part of my fascination with pharmacology stems from not just the compounds, but the plethora of ways those compounds can land on the human brain.
I just found a connect of "real #3 H" and then it went grey on me & it took too long to hit me. Real H hits immediately snorting or shooting. Of course a better rush is available shooting, but still snorting real H hit quickly being a highly lipid construction.
H always took like, sub-15 seconds for everybody including myself also, when you say it went grey though do you mean it literally changed colors at some point? If so, under what conditions?
Whatever, street drugs are never where it is at and I am done playing games with smoke shops and lying runners. I can't fuck in the nail salon all day, I spend all my profits and won't live long.
I completely agree with this sentiment, it's why I really think that building the habit of saving samples of batches for analysis is important.
