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What is wrong with the MDMA available today? - v2

Oh yeah I have more to respond to from one of your earlier posts on this thread regarding what you call “objective proof of meh-MDMA's existence”.
What would you consider an objective proof of its existence without identifying the culprit, e.g. a contaminant ?
Is the alternate psycho and physiological profile of effects described in the first 2 posts of this thread insufficient ...especially in MDMA-naive users?

Just to make sure we are on the same page: We are discussing the evidence for existence of Meh-MDMA, aren't we ?.

You are a perfect example of someone on this thread not grasping everything and not being aware of how actual science works. More on that below,
...Valid in what world and to whom?
In this world and to people following the scientific method.

How is a different Mydriasis ratio different form a darker stripe on an immunoassay plate designed to detect the culprit, e.g. a potent contaminant ?
I will grant you that the chemical reactions in the in-vivo test are much more complex than in the in-vitro reaction of an immunoassay test ...but does that difference in complexity invalidate the qualitative difference between reactions to clean MDMA and Meh-MDMA ?
 
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Firstly, “meh” MDMA is a highly subjective, qualitative, unscientific term.
Granted but we have to call it something short or keep repeating the long phrase, such as: "substance which most laboratory tests identify as racemic 3,4-MDMA Hydrochloride but which exhibits alternate psycho and physiological profile of effects in most human patients".

In no respectable paper in any serious journal will you find reference to "meh MDMA" or any variations of this term marrying the informal “meh” as a qualifier to the chemical shorthand of “MDMA”.
Yes, this is just a moniker that evolved on this forum. In the beginning it was called "Mongy MDMA", which was still much concise than a "substance which most laboratory tests identify as racemic 3,4-MDMA Hydrochloride but which exhibits alternate psycho and physiological profile of effects in most human patients".
Just because its name is colloquial does not invalidate it existence. It is just a shorthand.

Secondly, everyone already knows that impure MDMA that results in a less than optimal MDMA experience exists. It's not a new thing; it has been around as long as really pure, excellent MDMA has. Both are still out there on the market as many MDMA labs all over the globe still exist.
Yes, but not all impurity profiles have the same neuropharmacological profiles.
Sample hypothesis/possibility: the impurities from a sloppy MDMA synth from 3,4,-MDP2P Glycidate are not the same as impurities from a sloppy MDMA synth that obtains the 3,4-MDP2P intermediate from Safrole or Piperonal. The former impurities might generate the Meh-MDMA effect profile and the latter do not.

Thirdly, are you forgetting what “objective” versus “subjective” means? HowTF is one person, one subject – @indigoaura – how is that one subject's experience “objective” in any way?
I do not forget the distinction between the subjective and objective.
The alternate physiological profiles like Mydriasis, Trismus, BP. temperature and fasting glucose metabolism are manifestations of the alternate effects profile which can be measured objectively.
The psychological effects are very difficult to measure objectively without a large cohort and reliable double-blind surveys (the onset and duration time might be easier to measure objectively, though).
The alternate effects profile listed by @indigoaura is not derived only from her experiences but also from experiences of other people. (including MDMA-naive people which rules out tolerance issues). I have also conducted in-vivo tests which demonstrate this and I described them in these threads.

Why would this be unfortunate? And why the comma here?
Because in-vivo tests require participants that risk their health to test a substance. Also MDMA-naive "Guinea Pigs" are good only for one test.

That's the only biological data you would base this on? Do you have any idea what you're talking about, and have you conducted any actual scientific studies funded by some grant, private company, or university? I suspect you're speaking about things you're not experienced in yet.
No, there are several physiological data points that I considered.
Yes, I have done experiments. Why did you bring the size of the source of funding into this question, anyway ?

Again: “meh-MDMA” is a colloquial term, not science.
Yes, it is a colloquial moniker, but the alternate effects profile that stands behind this term is not unscientific not does it preclude a scientific approach to discovering its cause.

You would have to define the actual compound(s) in question, state how you verified the compounds, and list their IUPAC names. “Meh-MDMA” would not suffice.
That is needed to define the cause of Meh-MDMA's existence, not proving its existence. You seem to be conflating these two issues.

Also, it's worth delineating here what you mean by, for example, “MDMA + 2CB” and how it differs from “2CB + MDMA”.
I meant it in the context of @indigoaura 's experience, in which the order of administration of these two substances produces different effects when Meh-MDMA is involved. Please scroll several messages back before my answer, where she describes that difference.

I assume you're talking about candyflipping, meaning to say taking one, waiting until just after the peak and the piggybacking the other one.
No, no - I was referring to the observation which @indigoaura has made that Meh-MDMA affects the 2CB experience different;y than the clean MDMA. The different interaction between these two drugs is a significant data point.
 
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Granted but we have to call it something short or keep repeating the long phrase, such as: "substance which most laboratory tests identify as racemic 3,4-MDMA Hydrochloride but which exhibits alternate psycho and physiological profile of effects in most human patients".


Yes, this is just a moniker that evolved on this forum. In the beginning it was called "Mongy MDMA", which was still much concise than a "substance which most laboratory tests identify as racemic 3,4-MDMA Hydrochloride but which exhibits alternate psycho and physiological profile of effects in most human patients".
Just because its name is colloquial does not invalidate it existence. It is just a shorthand.


Yes, but not all impurity profiles have the same neuropharmacological profiles.
Sample hypothesis/possibility: the impurities from a sloppy MDMA synth from 3,4,-MDP2P Glycidate are not the same as impurities from a sloppy MDMA synth that obtains the 3,4-MDP2P intermediate from Safrole or Piperonal. The former impurities generate the Meh-MDMA effect profile and the latter do not.


I do not forget the distinction between the subjective and objective.
The alternate physiological profiles like Mydriasis, Trismus, BP. temperature and fasting glucose metabolism are manifestations of the alternate effects profile which can be measured objectively.
The psychological effects are very difficult to measure objectively without a large cohort and reliable double-blind surveys (the onset and duration time might be easier to measure objectively, though).
The alternate effects profile listed by @indigoaura is not derived only from her experiences but also from experiences of other people. (including MDMA-naive people which rules out tolerance issues). I have also conducted in-vivo tests which demonstrate this and I described them in these threads.


Because in-vivo tests require participants that risk their health to test a substance. Also MDMA-naive "Guinea Pigs" are good only for one test.


No, there are several physiological data points that I considered.
Yes, I have done experiments. Why did you bring the size of the source of funding into this question, anyway ?


Yes, it is a colloquial moniker, but the alternate effects profile that stands behind this term is not unscientific not does it preclude a scientific approach to discovering its cause.


That is needed to define the cause of Meh-MDMA's existence, not proving its existence. You seem to be conflating these two issues.


I meant it in the context of @indigoaura 's experience, in which the order of administration of these two substances produces different effects when Meh-MDMA is involved. Please scroll several messages back before my answer, where she describes that difference.


No, no - I was referring to the observation which @indigoaura has made that Meh-MDMA affects the 2CB experience different;y than the clean MDMA. The different interaction between these two drugs is a significant data point.
sloppy MDMA synth from 3,4,-MDP2P Glycidate are not the same as impurities from a sloppy MDMA synth that obtains the 3,4-MDP2P intermediate from Safrole or Piperonal The former impurities generate the Meh-MDMA effect profile and the latter do not.

This simply isnt true. And take want you want to believe but I sourced safrole from X big manufacture in 2016/7 with no restrictions on buying under a more cryptic name. .After being burnt on "safrole" so many time, it was eventually confirmed by NMR, though I have found it from time to time with other people that smell is undeniable good once you know .
SO I defiantly have had known SAFROLE MDMA that was for sure MEH. it also looked like garbage and i'm pretty sure I posted that NMR I think and also a pic of the meh product. But that's besides the point. You can defiantly have safrole based MDMA that is meh. Might be less likely because if you know how to source nitroethane that is ethane not methane piperonal and safrole in the USA with little regulation, you probably have a deeper understanding of chemistry anyways and can probably make it from unwatched reagents or weird RC's rearrangements or unknown precursors

If my notes/memory are correct he used the wacker from some pdcl2 he had awhile back. He made his benzoquinone . However it was meh MDMA. I had seen product like it from the darknet as well. But this was private lab and about 3-500ml of NMR confirmed safrole was gifted to this lab.

If I remember wacker caused oxygen double bonding issues or something making meh. But I don't remember what extaly it is/was the main issue on that route.
 
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SO I defiantly have had known SAFROLE MDMA that was for sure MEH.
I never wrote that MDMA synthesized from Safrole is always devoid of deleterious impurities. There are many way to mess up a synth and many ways the precursors/reagents can be contaminated. However, I think that certain reactions are more likely to be screwed up than others and some precursors are more likely to be contaminated than others ...or more likely to generate synth byproducts. The synth methods and precursors have evolved over time and somewhere before 2010 they changed for the worse.

I am sure a good chemist can make a good product even out of very dirty precursors using even very error-prone reactions.
 
@unodelacosa

I'm mostly going to respond to the meta-narrative that just occurred between us, as I really have no interest in further arguing points - especially considering how numerous and specific they just became :p

I am not taking this as seriously as it seems you think I am taking it. It seems like you interpreted my post as making a blanket statement that you are self-righteous and dug into your perspective, and that the reactionary nature of my post was done out of unconscious defensiveness.

While I attempted to, and I think succeeded to some degree, convey the context within which I was making my statements, and the limited nature of said contexts, I don't seem to have done a good enough job. As simply as possible, the responses that I made were solely in response to the quoted statements above; I did not intend to make judgments of your overall character, behavior, or thoughts. I apologize for becoming a bit self-righteous myself, and in no way was I attempting to diminish the contributions you've made to this thread.

I agree that many of the points you have made are worthy of consideration, I disagree that many of them are true - maybe more accurately, relevant? - and I really don't have any problem with you or our disagreement any further than the small passionate remarks, made in the original post I replied to, stating that this endeavor is a crock of shit. My response having been influenced by my dislike of such a small comment reflects an orientation to discussion here that I actively discourage and express disdain for, and I apologize for that, as well.
 
i wish i could read all this to see what you guys are actually arguing about but i start reading it, and then i just skim to the next message and read the first sentence and then skim to the next one

is it just me?
 
is it just me?
Yes it is! 🤣

Only joking.

If that were true these two MDMA threads wouldn’t be anywhere near as long as they are. And I could probably say the same for a lot of CEPS threads too.

I’m not complaining (just for the record). But then I have the time I guess.

It’s no secret that I read these MDMA threads i.e. MDMA just never been on my radar but keen to see the resolution from a pharmacological standpoint.

But given that I’m no chemist I just read and stay quiet.

While I’ve broken silence and cover though: there is one thing that pops into my head every time there is an update or argument:

There’s at least one person here that is capable of synthesising the real deal.

Would it not be possible for same to revisit their old hobby and synthesise a small batch and then pick, say, five members that are experienced and are sure about the fact that there is a problem with today’s stuff vs. that of yesteryear and let them try it and report back? That, if nothing else, would prove a point and either reinforce or dispel any myths. It would not, of course, solve the problem from a pharmacological point of view. If successful though: maybe said MDMA could be used as a reference to compare to the shit stuff using the various scientific methods and laboratories.

From what I see: those that know their oats on this stuff are probably in a position to contribute toward the cost of the project?

I’m not by any means suggesting that anyone revisits their chequered past and starts a business. But seems a pretty simple and practical way to at least remove doubt or any subjectivity from the problem.

As for the practicalities, availability of precursors, and what ever else is required: I cannot comment. This all way above my pay grade.

And so very sincerely: not by any means encouraging an illicit trade or business. There appears to be a legit issue here. And I make the suggestion purely in the name of science and nothing more.

If this just dumb, unpalatable, or unacceptable just shout i.e. don’t quote this post and I’ll delete it.
 
I think people are drastically overestimating the total number of people participating in these threads by only looking at the page counts. The vast majority of posts in them come from the same small group of posters. Pick a random page in it and you are going to recognize most of the usernames. Personally I probably have at least 200 posts in the old thread, and I was far from the most active user.

Rather than getting into the complications of synthesizing anything, it seems like the easiest thing would be for samples of the most "meh" lab confirmed MDMA people have encountered to spread. We could all take selfies holding calipers against our pupils and at least resolve the existence question within a month.
 
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We could all take selfies holding calipers against our pupils and at least resolve the existence question within a month.
Calipers measure the absolute size of the pupil.
However, people's eyes are different sizes so we need a relative measurement. Since the outside diameter of the iris stays constant regardless of lighting conditions, the diameter of the dilated pupil can be compared to that. For that, only a closeup selfie is needed and controlled illumination.

Also, there is a group of people who genetically do not respond with Mydriasis to amphetamines nor MDMA. This group is a minority.
 
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Yeah and to resurface a report from a few months ago, we have had reports of people having different dilation reactions to the exact same suspected MDMA:

I found an interesting report on Reddit where two people had different responses (some partially matching those described here) to the exact same substance.
We dropped around 9 last night and blew up together around 10. I’m very small and he’s like, three times my size, so obviously he took more than me. We’d had the same day, ate at the same time, smoked the same weed throughout the super relaxing lazy day, then decided we wanted to roll for our night out with friends.
We’re pretty experienced with molly and always get crystals - the ones we got this time weren’t entirely clean, but, like I said, we have some experience under our belts. We didn’t shy away. Anyway, he was the usual high-energy, pacey, massive pupils, super thirsty, stimulating conversation high.
I, however, had the weirdest roll of my life. My pupils never dilated, but I was feeling it. I definitely blew up. I felt the usual high internally, but my body was just melting. I spent the whole night sitting in silence. Once we got home, I got super cold and had to lay down with several blankets. Sorry if this is TMI, but once we get home, we usually ride out the high literally. Just hours of intense sex. We still did plenty of that well past sunrise, but I was just physically exhausted and my eyes were so heavy.
He never fell asleep and the poor thing had to go to work. I slept maybe a collected... 4 hours? But I kept having these rapid fire absolutely horrifying nightmares. Just one after the other. By the time I drove him to work (I didn’t want to chance him having to drive home alone tonight) we were seeing neon tracers coming off of everything.
It certainly wasn’t a bad time. I felt fine on the inside. I was just super weirded out by the physical part of my high. I also was ravenous and I’m NEVER hungry on molly. I couldn’t eat because my throat wouldn’t let me, but my stomach was growling the entire night.
Has anyone else experienced a high like mine? Like I said, I’ve taken mdma plenty of times and literally have never had a high like this one. Super odd.
Bolds are mine

When they say that their pupils not dilating is part of it being the weirdest roll of their life, I assume that they normally experience full pupil dilation.
 
Calipers measure the absolute size of the pupil.
However, people's eyes are different sizes so we need a relative measurement. Since the outside diameter of the iris stays constant regardless of lighting conditions, the diameter of the dilated pupil can be compared to that. For that, only a closeup selfie is needed and controlled illumination.

Also, there is a group of people who genetically do not respond with Mydriasis to amphetamines nor MDMA. This group is a minority.
I have notice earlier today, much larger pupils in myself on only 150 ug LSD, than I observed in myself on 600 ug 4 days ago.

I make minimal, only fleeting observation of it, but it has intrigued me personally of late through extensive LSD Macrodosing.

My pupil size varies and can look perfectly normal in proportion, size on even 1000 ug doses, though even small pupils have got that “Black Holes in the sky” thing going on.

But I can be fully up on LSD with normal size pupils, and vice versa.

But regardless, simply going by all past experience of “undisputed” MDMA, I think it was rare to be up on a dose of 120 mg’s MDMA or more, without real saucer eyes. More so, and more consistently with real MDMA than LSD possibly.

Yes “Meh” is unscientific. My word is dispute. Real MDMA is indisputable. I still can’t even imagine us ever having felt the need for this dispute, between late 97 until May 2005 after a 96 lull in quality and potency, while the whole market was still a flood with original Doves, Elephants, Dolphins etc, by 1998 standards picked up.

“Shit” pills were always to be found. My very last MDMA pills May 2005- Mickey Mouse!!!

They were not the same MDMA I took predominantly over those 9 previous years.

There was something terribly suspect, not right, about those Mickey Mouses.

If every single MDMA pill now was identical to....OG 90’s white Doves, Dolphins, Elephants, the best Mitsubishi’s, Smiley faces, Blue and yellow Bentley’s, too many others to recall here I would take to my desert island basically, again, no way could we ever be having this discussion.

Simply no way.
 
It's pretty much universally accepted that any drugs advertised as included in pressed MDMA pills are not actually there, ala heroin and mescaline. Those are two of the most frequently claimed ones, so far as I'm aware. Generally, except for isolated instances, the only other substances, that I'm aware of, that have been included are byproducts, MDA, bk-MDMA, PMA, caffeine, and methamphetamine.

RE: Mescaline specifically, vash is correct that Mescaline is way too rare and expensive to ever be in pressed pills unless they were a small passion project by a chemist who cares, etc. I'm pretty sure synthetic mescaline is above $100 a gram (don't think I'm breaking pricing here necessarily?), 100mg isn't enough to do much, and so including say 200mg would be hugely increasing cost. Also, you say the MDMA felt like Mescaline. Well, that makes sense. Mescaline and MDMA hit a lot of the same receptors.
Surely it’s accepted though, as an example, that DMX was sold as ecstasy in later 90’s in the four leaf clover Shamrocks?

I believe in DXM presence in “ecstasy” pills over time.

I also believe the muppets pressed ketamine to sell as MDMA, even in 90’s.

Which is pretty dumb really. DXM I can get but I think there were some bad reports involving those Shamrocks. I only saw them once in 1999, but declined as BANGING Mitsubishi’s were literally never more than 20 foot away.
 
Did you control for the illuminaton level and duration of exposure to that illumination level ?
I’ll try to answer that honestly. No controls as such, just my observations and consequent curiosities.

I had saucer eyes on today’s 150 ug trip, but not on 600 ug last mid-week.

And it’s not a given that 1mg will enlarge my pupils even as much as the 150 ug today, but it could well.

It just seems to vary. Regardless of effects, visuals and mindset.
 
The magic that you refer to, IMO, is the ecstasy that was produced from sassafras.
Safrole as a starting precursor is not what determines product quality. Organic chemistry is all about reaction optimization and purifying target compounds and intermediates. The most common synthetic routes to MDMA often start from sassafras oil which contains safrole. This is isomerized to isosafrole and converted usually to a ketone intermediate like MDP-2-P (aka PMK). Sometimes a chemist might be lucky enough to source PMK and save themselves the trouble of first working that up, but “lucky” is the operative term there… and then reductive amination with cleaning and workup via several methods, sometimes using an oxime intermediate, but I've always been a fan of Shulgin's preferred route – Al/Hg amalgamation.

There are a lot of variations within this broad scope of production. This is where impurities come into play, but it's not because sassafras was chosen as the starting material. It's more to do with the synthetic route performed and how skilled the chemist is at pulling this off under clandestine conditions. Oftentimes, the clandestine chemist is forced to manufacture their own precursors and reactants before they can perform the main reaction to desired to produce their target compound. In the case of P-2-P → methamphetamine as well as in the case of MDP-2-P → MDMA it is often necessary to produce one's own methylamine. During that process, dimethylamine and trimethylamine are easily produced side-products, and care must be given to minimize this unwanted effect and then later to purify one's methylamine from its dimethyl and trimethyl counterparts else this can easily result in MDDMA and MDTMA side-products. This is merely one of many various impurities that can form, but studies in rat brains have discovered that these two particular compounds can ultimately have a negating, dampening effect on MDMA's profound psychotropic changes associated with its use.

Regardless, when people speak of “P-2-P Meth” or “Biker Crank” versus “Ephedrine Meth” / “Nazi Cook Meth” / “Birch Reduction Meth” or “RP/I/E meth”, “Red, White, and Blue Cooked Meth”, or “Nagai Route meth”, the key distinction is that P-2-P meth is a racemic mixture, aka dl-methamphetamine. Meanwhile, Nagai's HI Acid Reduction and The Birch Reduction or just about any method that reduces ephedrine (or pseudoephedrine) is usually stereospecific and produces enantiomerically pure d-methamphetamine. The “d” and “l” here stand for “dextrorotatory” and “laevorotatory” and refer to the fact that the dex isomer spins light to the right while the “laevo” spins light to the left. It isn't a coincidence “left” and “laevo” both start with “l”, and also the word “dexterity” refers to “dominant handedness” (on the assumption the whole world is, or should be, right-handed as people superstitiously believed long ago).

That's a lie... BECAUSE I HAD safrole based mdma that was self synth/private lab with locally sorced SAFROLE by xxxxxx (big lab company that will sell to anyone
So? This doesn't mean the chemist knew what they were doing and how to get from safrole to MDMA without introducing and accidentally producing impurities along the way, some of which might have a counteracting effect to MDMA.

if they really want safrole anyone can get in the usa no questions asked
PLEASE NOTE: This is definitely not true. While I believe you, @vash445, as far as saying that somewhere in the U.S. people can obtain sassafras oil and/or safrole, this is NOT safe to do, legally speaking, as it's definitely against the law and the seller is definitely required by law to report any and all sales of a List I chemical precursor such as safrole (3,4-methlenedioxyallylbenzene) to the DEA. Does every chemical supply company do this? Probably not, but I fucking PROMISE YOU and anyone reading this that many—perhaps most—suppliers do report these sales to the DEA and that alone is enough for a federal judge to sign off on a search warrant. Ignoring this and just ordering safrole all willy nilly will have The Man knocking down your door before you can say “root-beer-scented candles, I swear!”

It was meh mdma. Came from safrole . It is def not safrole... it had a really funny nmr once tested.it is no doubt an impurity. MAPS also uses piperonal in their synth and they don't have the meh issue.
Listen, safrole is distilled from sassafras. Safrole is aka 3,4-methylenedioxyallylbenzene. Notice the 3,4-MD… part is already in place.

Isomerizing safrole to isosafrole is just a simple, gentle reflux, and then piperonal can be produced via oxidation of this isosafrole.

It's also possible to get to piperonal, phenyl-2-propanone/PMK, etc. starting from 1,2-methylenedioxybenzene or even from 1,2-dihydroxybenzene but that's starting from even further back, route-wise, than safrole because it requires one to produce a Williamson ether using dichloromethane.

Whatever “meh” MDMA is attributable to MDMA impurities formed during synthesis, then MAPS likely doesn't have that particular “meh” issue because whoever produces the MDMA for their studies is a proper chemist who knows proper lab techniques, has the requisite knowledge, and can competently use analytical tools that they also have access to in the first place. Meaning: the reason pure MDMA is pure is because a knowledgeable and skilled chemist equipped with the right equipment produced it, not because some chemist started from piperonal or any other chemical, per se.

____________________

To both you, @vash445 and @OrbitalCombustion@vash445 is 100% correct in their assessment that MDMA is never cut with mescaline. This is true for many reasons, not the least of which is that it is quite rare and expensive to find these days. Mescaline is not squandered by attempting to pack hundreds more milligrams of active product along with ~200mg of MDMA. If a clandestine chemist has access to microcrystalline cellulose (MCC) that presses up to 2:1 inactive-to-active, then this is entirely possible though still not probable again due to fiscal reasons and rarity. If the chemist only has access to lesser bonding agents and may or may not have stearic acid, then the ratio goes to 3:1 or higher and they'd have massive, triple-stack, crumbly mescaline-and-molly pills, which, Idk if you've ever dealt with crumbly pills, but god-fucking-dammit, man, that's a pet peeve of mine. However, once again this is possible, but nothing I've ever seen. Doesn't mean it hasn't happened, but from a profits-driven perspective, it doesn't make financial sense, particularly as so few people would even know they were having mescaline in the first place. So even if a clandestine chemist were so inspired to put out a batch like this, it would be a stupid and mostly pointless attempt at turning on others to mescaline.

There have been probably about a half dozen times in my life where people have sworn this or that pressed pill contained mescaline. Having experience with mescaline—while I could never be certain since it was just my subjective perspective coupled with a skeptical attitude going into it—to me, none of the pills alleged to have mescaline had any real mescaline. Likelier substitutions: MDA, 2C-I, 2C-B or some other, potent, psychedelic phenethylamine or tryptamine possibly mixed, or not, with MDMA. Similarly, many people think microdots are mescaline instead of acid. They aren't. A strong mescaline trip involves consuming ~500 mg of the sulfate or ~400 mg of the hydrochloride.

Personally, if I want mescaline I extract it from dried San Pedro clippings. It's kind of a pain in the ass dealing with all the various plant fats and chlorophyll and their resulting emulsions, but there are techniques around all of these obstacles, and it's a lot cheaper than ordering an international shipment… (that said, [mod-snip]some vendor's[/mod-snip] products are top fucking shelf, believe that).

EDIT: tried correcting any gender pronoun assumptions I made; apologies if I've gotten any of them wrong.

EDIT 2: regarding / more on mescaline —> mescaline isn’t particularly difficult to synthesize, or at least no more or less so than any other phenethylamine – it’s 3,4,5-trimethoxyphenethylamine (TMPEA). I consider LSD to be more difficult as it involves chromatographic purification, working swiftly under low, red-light or yelllow-light conditions, the possession and use of a rotovap, and various other hurdles. The trouble from the clandestine chemist’s perspective is that, from the same starting material, it‘s about equally as challenging to produce 2C-B, 2C-I, or even possibly DOM, DOC, DOI, DOB, and/or TMA-2, all of which are much more potent, mg for mg, than mescaline.

So let’s just say for argument’s sake, starting from the same 8 kilograms of precursor allylbenzene, you could produce 5 kg of either mescaline or 2C-B comfortably.

With mescaline, 5,000 grams = 12,500 doses @ 400 mg per dose or 10,000 doses @ 500 mg per dose.
With 2C-B, 5,000 grams = 200,000 doses @ 25 mg per dose or 166,667 doses @ 30 mg per dose.

So we’re talking about sixteen times the total yielded doses from the precursor. Granted, I’m simplifying, and these numbers are ballpark, but Mescaline doesn’t provide much incentive to the clandestine chemist to produce and promote when much more potent psychedelics exist.

LSD is even crazier as 5 kg of pure LSD is 50 million doses at 100µg per dose.
 
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Lol, it definitely is what it is. Crap. To say there’s nothing wrong with today’s MDMA tells me one thing...you haven’t done any ecstasy pre-2010.
No, it tells me you haven't been able to find good MDMA since 2009. Your experiences are not universal to everyone else, and I know you know this, so this is just a reminder… believe me, there are many MDMA producers in the world and they have varying degrees of skill and use different methods, equipment, and chemicals, all running the gamut from kitchen and hardware store stuff to professional-grade equipment.

If the only car I’ve ever driven in my lifetime was a Ford Focus, I would think the Ford Focus was the best car in the world.
You mean the Ford Focus isn't the best car in the world? Lol, well they probably have good fuel efficiency… Regardless, this analogy kinda sucks. I get what you're trying to say, but if you drove a Focus, it's still likely you would be aware that “better” vehicles exist and, if your desire to drive a finer car were sufficient enough, you'd figure a way to source a whip you liked better… just as I encourage people to seek better MDMA if they're indeed only finding crap.
 
I apologize for becoming a bit self-righteous myself, and in no way was I attempting to diminish the contributions you've made to this thread.
This is kind of you to acknowledge, and I appreciate it.

stating that this endeavor is a crock of shit
No, I'm sorry, I must've phrased things idiotically. It was never my intention to state that this endeavor is a crock, I was talking about people drawing simplistic conclusions from what is clearly pretty goddamn complex considering the subject matter at hand, something that many of us are very passionate about and find infinitely interesting, as I do, and so do @vash445, @user666, @indigoaura @AutoTripper @dalpat077 @Mr. Krinkle, @Le Junk (much love and respect to you all; even if I harshly disagree and it seems like I'm going hard in the paint on you, I swear it's just how I debate, so please know that I respect you all) … and others I've read intelligent posts from just on this thread alone. … It's funny: the thought occurred to me that perhaps that wording was going to make someone angry or offend someone for taking it too personally. I hope you accept my apology then for my careless wording, and trust that I'm being sincere in my words above.

Alright, @user666 … I've got a lot of responding to do to you now, but chiefly I think you've misunderstood me in a few places as well. Just to reiterate, I'm not questioning the existence of MDMA impurities, and the reason I'm complaining about the term “meh MDMA” and its more clever portmanteau word forms, is that it lacks precision and could quite possibly refer to a number of different impurities, and that's assuming it's widely accepted that the cause of so-called “meh” experiences is solely caused by impurities. I just don't think it's likely you're going to find enough mass agreement on the cause.

From reading this thread, I've definitely learned some new things. For example, while I knew of the existence of MDDMA and MDTMA, I did not know about the specific binding properties of both compounds and the unique variability in receptor preference regarding the dimethyl analog. It would be super cool if we could safely attach radio isotopes to these compounds and then (again, safely) use x-ray imaging to observe their paths through the human brain, wouldn't it?

Granted but we have to call it something short or keep repeating the long phrase, such as: "substance which most laboratory tests identify as racemic 3,4-MDMA Hydrochloride but which exhibits alternate psycho and physiological profile of effects in most human patients".
Ok so I get that hyperbole can be effective, but you know goddamn good and well you made that phrase obnoxiously long, and furthermore I never suggested this should be done at all. Hell, if anything, I think we can narrow down quite a bit to MDDMA and MDTMA as the two culprits worthy of the most pursuit right now in terms of identifying whether they've been widespread throughout most of the world's MDMA distribution networks as the result of poor/sloppy synthesis. This is entirely plausible, but once more, I don't see how this could be proven easily and unambiguously as you'd need a lot of corroborating seizure evidence data and testing facilities would need to be adequately equipped to distinguish MDDMA from MDEA which have the same molecular weight and basic configuration/shape.

It's the nature of clandestine chemistry that gathering data from most, if not all, the major underground MDMA chemists in the world is probably virtually impossible. That's just conjecture though; who knows?

Just because its name is colloquial does not invalidate it existence. It is just a shorthand.
Yeah no shit, Sherlock; I'm not attacking the shorthand phrase. I'm saying there are assumptions and unproven statements in the phrase you claim it's shorthand for, to wit: “substance which most laboratory tests identify as racemic 3,4-MDMA Hydrochloride but which exhibits alternate psycho and physiological profile of effects in most human patients”. Let me break that down.

“substance which most laboratory tests identify as racemic 3,4-MDMA Hydrochloride but which exhibits alternate psycho and physiological profile of effects in most human patients”

Just a better wording alone would give us:

substance identified via [method used, e.g.: HPLC, GC-MS, whatever] as racemic n-methyl-3,4-methylenedioxyamphetamine possessing an alternative [not “alternate” which means “every other” in science parlance] psychostimulant profile of qualitative effects in some human subjects according to anecdotal reports.

You can't so easily make a claim like “most human patients” without any properly gathered statistical data and expect to be taken seriously.

substance which most laboratory tests identify – “Most” lab tests? Ok so not all lab tests, then? What do the other tests identify? I seem to recall @indigoaura talking about MDEA contamination, and as has been discussed, distinction between MDEA and MDDMA is notoriously tricky given their identical atomic weights and imperial formulas. If a lab detects 100% pure dl-MDMA (it's not really necessary to mention the optical isomers, nor that we're discussing the racemate MDMA, and of course it's also assumed the methylenedioxy ring is on the 3- and 4-position unless noted otherwise, but I guess you were attempting to be satirically wordy), then there is zero reason why someone shouldn't have a full-on “magical” MDMA experience according to the “some-impurity-is-causing-meh” theory.

@indigoaura couldn't understand why pills he's had tested by Energy Control International in Spain seem to show only mostly the expected MDMA and I think there was a mention of MDEA as well, but don't quote me on that. The bottom line though is that IEC didn't have an analytical standard for n-dimethyl-3,4-methylenedioxyamphetamine (and assumably neither do they have one for n-trimethyl-3,4-methylenedioxyamphetamine). Until they have this standard, they cannot accurately test for MDDMA and MDTMA, which seems like the two compounds this thread has more or less settled on pursuing, and I have to agree with the logic of doing so as these compounds have already been proven to blockade the serotonergic activity of MDMA.

Will this account for EVERYONE'S so-called “meh” experience? Who knows? You'd also have to have your pills and powders sent to IEC to know with any certain, and again, only after they have the analytic standards and also contingent upon trusting that the folks at IEC know what TF they're doing… which they probably do, but I sometimes I see a serious lack of skepticism around here… I'm encouraging everyone to remain skeptical until you're certain, and to keep your expectations realistic.

What would you consider an objective proof of its existence without identifying the culprit, e.g. a contaminant ?
There is no such thing. Identify the culprit and I'll call that objective proof of its existence. You can't tell me that you think “most people” aren't experiencing MDMA as they're supposed to without telling me any of the numbers behind “most”, quoting an assorted pile of anecdotal trip reports, and not be able to identify the substance responsible, or as you put it: “the culprit”. Think about what you just asked me for a minute: what would you consider exists despite not having empirical, testable, identifiable proof of said existence? Let's see, there's God, Santa Claus, the Easter bunny, the Loch Ness monster, Frankenstein, the Flying Spaghetti Monster, and an invisible, weightless impurity in MDMA.

Unless I'm mistaken, “meh MDMA” refers to any street sample of purported “MDMA” that consistently and widely renders easily noticeable subpar qualitative effects in human users for reasons yet unknown. @indigoaura narrows this scope by claiming that “meh” product (note: the “meh” quality is something we have to take people's word for here) tests as mostly MDMA and believes whatever as-of-yet-unidentified impurities hold the mystery to what's causing his disappointing experiences with these particular batches. “Meh” does not refer explicitly to one substance identified as 3,4-methylenedioxymethamphetamine because that's fucking stupid; it is already called MDMA. The “meh” is the combined product it sounds like, most likely, of MDMA and something else.

Why did you bring the size of the source of funding into this question, anyway ?
No one mentioned the size of the source of funding. I was giving a few examples, the sizes of which can vary quite a bit. Moreover, @indigoaura has stated that the goal of this endeavor is to secure research funding. Who do you think is going to provide that funding, champ champ?

but the alternate effects profile that stands behind this term is not unscientific
I beg to differ. The “effects profile” you mention as deriving from “meh MDMA” – have those been determined in a double-blind study, then? No. These are all still anecdotes, which while they have some scientific significance, I cannot call these science in general though. It's kinda like how, researchers might read a lot of anecdotal trip reports from Erowid before conducting a study. They might mention this in the resulting paper, even quoting some of the anecdotes, but it's a huge stretch calling just that alone “science”. But you know, whatever, man. I don't really feel like arguing semantics.

That is needed to define the cause of Meh-MDMA's existence, not proving its existence. You seem to be conflating these two issues.
In a casual sense, proving meh-MDMA's existence isn't too difficult. Nearly everyone has had shitty MDMA before that definitely felt like it had some MDMA in it, but also some shit was just off. That's fine. No arguments outta me over here; I've had plenty of these experiences myself. Since then, I've had PLENTY of awesome MDMA experiences, too. So I reject the notion that ALL MDMA in 2021 is meh-MDMA which some people on here seem to believe. Also, just because I agree that it certainly seems like shitty MDMA is out there as do hundreds or even thousands of people, that does not scientifically confirm it exists, nor have a seen a proper poll conducted on a wide-enough sample of subjects. Correlation does not prove causation, so you have to produce actual empirical evidence that meh-MDMA exists, even if in our hearts we all already know it's super likely that it does. That's what science is for. Prove this without relying on subjective reports. To do this, you'll have to show how this happens. You need to define the cause of the meh-MDMA experience as this will prove its existence. I'm not conflating these two issues, they are causally related.

I meant it in the context of @indigoaura 's experience, in which the order of administration of these two substances produces different effects when Meh-MDMA is involved. Please scroll several messages back before my answer, where she describes that difference.
Firstly, I've read every single post in this thread. I've even scrolled through and read many of your posts to make sure I'm not talking to a moron (I'm not; you seem intelligent despite not understanding what I've been saying and that you and I agree on far more than we disagree). The order of administration is exactly what I was talking about as well… and using this as a test is even less objective while unnecessarily introducing even more factors that could skew the results. Changing the order of administration will produce different effects in general, no matter what the substances, but in no way does this prove anything about the two different “batches” of “MDMA” that wasn't already known – they produce different effects despite both being called “MDMA” by some vendor, IRL or on a DNM…

No, no - I was referring to the observation which @indigoaura has made that Meh-MDMA affects the 2CB experience different;y than the clean MDMA.
Yes, I figured that was the case even though it wasn't entirely clear at which exact point in the first drug's effects the user takes the second drug. This can affect the outcome of the two drugs quite a bit. On top of that, it's possible to consume both the first and second drug simultaneously at the exact same time… this is yet another way of experiencing the combined effects. Without accounting for these variables, this extra dataset means nothing. Too many factors, and everything is a variable, no control. Give me a break – if you say you've been involved with actual studies, you of all people should know better than to quote this nonsense to me like it's any real proof of anything other than people are getting swept up in the pseudoscience fringe opinions being slopped all over the thread like it's scientific canon.

My hunch – and I'm qualifying this by saying this is just an educated guess – is that @indigoaura, et al. just might be on the right track in suggesting MDDMA and MDTMA contamination is common enough to be blamed for many—anything from 15% to 60% is my pure speculation—suboptimal serotonergic MDMA effects due to a potent countering effect brought on by MDDMA and MDTMA. I further speculate that poorly manufactured methylamine would be to blame for this. Btw, to whomever suggested wacker oxidations result in meh-MDMA, was that you @vash445 ?, I don't think you understand – wacker oxidations produce MDP-2-P, nothing bearing an amine (NH₄). Improperly made MDP-2-P that is not purified can result in other impurities, but whether said impurities are even active or if they have a blockading effect is something you'd have to know to conclude this causes the aforementioned meh experience ecstasy.

The different interaction between these two drugs is a significant data point.
Not really insofar as identifying a contaminating substance. This data has the same relevance as people saying, “yeah this MDMA isn't as good”. It's not adding new, meritorious evidence. There is no established standard for exactly how MDMA and 2C-B should feel taken in any order. You have to bring forward empirical evidence; ya know what I mean? I'm really not trying to be obtuse here, argumentative or difficult. I'm just trying to slow down everyone jumping to conclusions prematurely based on what I see. Also, 2C-B's effects can be thrown off by a variety of different substance. Try snorting some coke mid 2C-B trip, or taking virtually any dopaminergic stimulant. You won't be tripping suddenly. At least, that's the experience I have and have witnessed. So it's no surprise the combo effects are fickle, but it's not really clear evidence of anything worthy of note. We've basically already concluded that impurities and substitutions definitely exist in what is sold on the black markets as “MDMA”. Proving which impurities impede the effects the most and which impurities are the most widely spread across the globe seems like something that is not an easy undertaking and probably not worth the effort, but I'm open to the idea that I'm wrong here. Do you get what I'm saying now?
 
Calipers measure the absolute size of the pupil.
However, people's eyes are different sizes so we need a relative measurement. Since the outside diameter of the iris stays constant regardless of lighting conditions, the diameter of the dilated pupil can be compared to that. For that, only a closeup selfie is needed and controlled illumination.

Also, there is a group of people who genetically do not respond with Mydriasis to amphetamines nor MDMA. This group is a minority.

I'm not sure if measuring mydriasis is the best gauge of the MDMA response. And when I write that I don't mean to imply that I doubt it's true - I am genuinely just not sure.

But it's easy to do, and @user666's method of reporting the results as % dilation (relative to the size of the iris) is a good one. In the ideal world you'd measure %dilation in exactly the same lighting conditions before and during the MDMA roll, but practically speaking that probably doesn't matter too much - it would be fine to do before and after photos with roughly similar lighting. With enough data points it should be possible to make a correlation between meh/magic and %dilation. If it turns out that there is a correlation, that would make an excellent in situ objective test for meh product.

By the way, it's not only that people's eyes are different size - pupil size varies all the time and it usually differs between the two eyes. It's also affected by things like caffeine and alcohol. But again, this variability problem can be solved with enough data points.
 
I'm not sure if measuring mydriasis is the best gauge of the MDMA response. And when I write that I don't mean to imply that I doubt it's true - I am genuinely just not sure.
I’m generally not sure either, but if forced to guess, I would guess that while it’s an interesting biometric to note, it wouldn’t prove anything to correlate pupil dilation to a supposed “meh” experience or a “magic” experience, both of which conclusions are too subjective. However, it’s good that we’re getting closer to measurable, observable science that does not rely on subject feedback like science is all focus groups or something…

But it's easy to do, and @user666's method of reporting the results as % dilation (relative to the size of the iris) is a good one.
Well it’s something. But dilated pupils is not a surefire sign one’s MDMA experience is “magical” or whatever. It’s just one of many biomarkers that manifest inconsistently across the population.
 
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