until some analytical chemist decides to make this their PHD thesis, the answer chemically speaking will be out of reach.
Yeah except we're dealing with anecdotal reports of pills & powder from yesteryear, many/most—possibly all—of which are no longer around to test. We have today's product of course, but does it even matter? Fake, bunk, and counterfeit MDMA has been around since at least the 90s. And the answer to everyone's curiosity about MDMA quality will never be fully satiated, even if some young researcher gets the approval to do their PhD thesis on uncovering something that is not important enough to be attached to a financial incentive re: would-be MDMA synthesis, or deliberate substitution, or take your pick, bc what causes one person to say, "this is mehDMA," will be different from other causes for other people. As we've established, many things can cause suboptimal "MDMA" or "MDMA-like" experiences. The term "meh-DMA" is neither precise nor technical.
But what I was told by my best friend today, and the context which makes what he said so compelling, must be shared with all of you immediately.
Forgive me, but I'm already dubious and expecting this will be continued anecdotal evidence.
Same. Been doing drugs the same amount of time, and even used to manufacture MDMA around the turn of the century. If you lived on the east coast of the U.S., there's a good chance we did the same drugs, from Star Wars blotter and Lenny Pickard's liquid LSD to white Mitsubishis and Red Omega presses, "tic-tacs" and "disco biscuits" to "shwag" weed, reggie miller, red lob, etc., etc.
Chemistry though?
I have a law degree, been an criminal lawyer for two decades,
Respect
and I have been taking MDMA (whether pills or crystal) and methamphetamine continuously for 26 years. I have been a member of this site and contributed throughout this time (albeit fairly sporadically in more recent years) since December 1999 and my username and login has not changed.
Were you ever a Hive Bee? How about the ADC newsgroup? I'm only asking outta curiosity since we're so close in age, not implying anything if you are or are not familiar with what I'm talking about.
I have read every single post of every single page of this thread and its previous incarnations.
Same.
My best friend (who I have known for 27 years and who was my partner for nine of them) is the same age as me and this person has taken MDMA and methamphetamine this entire time too. From 1999 to 2009 we would have had all of the same pills and most of the same experiences. We have continued to take MDMA pills and crystal/powder and remain best friends to this day and have shared in many subsequent experiences since separating. My best friend has taken even more MDMA than I have, in fact way more, over the last 10 years. He has limited knowledge of this issue, no chemistry background and has no idea of the extensive discussion concerning it, that has been a feature of this forum and I am sure many others for years now.
I know where you're going with this and I understand why it's so compelling to you, specifically, but it's not any new evidence we don't already know about with regards to anecdotal experiences sometimes being the same, and sometimes not. It does not mean any new conclusions can be drawn from this subjective experience.
Before posting what I wanted to share, I must state these matters from the outset:
1. No one who has said that meh-MDMA is a real thing and exists has ever said that all MDMA is meh; on the contrary.
No, it's been asserted by a few ppl on here that they don't believe "real MDMA" exists anywhere anymore. You may have noticed my username a few times throughout this thread. I've argued directly against these assertions, yet they persist and ultimately ppl will believe what they want to believe, evidence be damned. So I dialed back the amount with which I care to argue about it, present comment notwithstanding.
2. Anyone who asserts that meh-MDMA is a real thing is saying that despite the massive doses in so many of the pills these days, when you got a pill in the earlier days that tested as MDXX and wasn’t a total fake (speed, Ket, chalk, etc), then provided the dose of MDMA in that pill was high enough (and back then then dose per pill was 50mg to 150mg at best and I know this due to many years of having been privy to the results of forensic laboratory tests for seized illicit substances and seeing the certificates with my own eyes since 2001), the experience was close to textbook, physical effects like mydriasis could not be hidden, the experiences were amazing, and indeed often life changing. You were buckled, looked buckled and literally needed to buckle up for the next few hours.
Can you prove this, or do you expect ppl to take other ppl's word for it such as your own and your homie? See, it really falls apart here. I believe you, especially the part about having performed forensic tests to establish per-dose amounts, but the term "buckled" isn't the medically precise terminology needed here, though as a slang term, I'm a fan… And it isn't like samples from the 1990's are still verifiably accessible.
3. Anyone who asserts that meh-MDMA is a real thing and cannot be explained by more subjective factors is asserting that there is something chemically different about what they are consuming - either it is:
- not MDMA, despite test results stating to the contrary, including government forensic laboratory results which must be exact to be able of sustain a prosecution relating to MDMA as opposed to some other similar chemical;
- that the MDMA contains a greater proportion of the R enantiomer of MDMA as opposed to the S and is not racemic as it always was; or
This has been covered already and there's zero evidence to suggest anything other than racemic MDMA is on the streets with
very few exceptions.
- (this being my personal view) that much of the MDMA consumed today - illicitly produced and packaged as it is and requiring no purification at any of the steps of production along the way
What do you mean "requiring no purification at any of the steps of production along the way"? This is not realistic for any known syntheses of MDMA I've ever heard of, never mind the fact that things like extraction and crystallization are themselves purification techniques without which the synthesis would fail and/or the end product will be too impure and toxic to sell, buy or use.
- being manufactured from different precursors (or let’s be clear pre-precursors)
This is not a term we use in chemistry. There's the precursor, the final product, and any number of intermediates products between the two. For instance, starting from the precursor, Safrole, an MDMA synthesis might go:
Safrole (allylbenzene precursor) → Isosafrole (intermediate) → MDP-2-P (intermediate ketone) → MDMA and then onto crystallization, acetone rinse and recrystallization.
This is not unusual, and it's similarly not uncommon for multi-step procedures to be performed in legitimate industry as well.
and using different reductive animation methods
I'm guessing this is a type and you know this next part, but for anyone reading along… So it's "reductive amination" because it's reducing (removing) an oxygen atom and replacing it with an "amine" (NH₃). Reductive
animation might be a stick figure cartoon…
than MDMA produced in those earlier days, contains some type of impurity or impurities or combination of impurities, perhaps within the umbrella of a “impurity family”, all of which have the capability of muting/shortening/ruining the true MDMA experience to varying extents; much like SSRIs have the capability to do by blocking the monoamine transporters especially the SERT, so the MDMA molecule cannot enter into the axon of the nerve cell to work its magic.
In the case of MDDMA and MDTMA—two byproducts from MDMA synthesis performed with impure methylamine containing dimethylamine and trimethylamine—this could be the case maybe, but it's unclear if, when, how often and prevalent this is. My best guess is that it's not but so common. For that matter though, MDMA itself begins to blockade its own activity, itself being a mild to moderate serotonin reuptake inhibitor. This is why, in a single session, subsequent doses are much less effective than the initial dose.
advocating for the existence of the meh-MDMA phenomenon
Think about that wording for a second. Either something exists or it doesn't, when discussing concrete real world objects. Someone might advocate for certain gun laws, for example, but no one "advocates" for the existence of coconut inebriation. You can advocate as hard as you want for it, but coconuts still will not ever get you high no matter how many ppl agree that it's time to trip balls on some coconut water. Similarly there's no advocating for the existence of meh-DMA. The phenomenon, as reported, surely exists, as much as placebo effect is very much a real phenomenon (not saying mehDMA is placebo, just that I'm not invalidating ppl's subjective experiences; I'm just arguing that the cause is unknown and most likely unknowable without refining some definitions and using more precise terminology to describe things. I know that seems like I'm arguing semantics, but words matter in that they affect perception in various ways through shades of meaning and the sort. I know you know this if you're a lawyer.
- pure MDMA-HCl is the same as any other PURE MDMA-HCl regardless of how it is made but we aren’t dealing with laboratories making pure illicit anything;
That's not true, check your facts. While many street drugs are lower than pharmaceutical-grade purity, this isn't always the case, and pharmaceutical products also wind up in the black market sometimes. Moreover, there are some very talented clandestine chemists out there who indeed produce such quality LSD, MDMA, and other staples of the drug panoply.
- pure 3,4-MDP2P can of course be made from any of the pre-precursors that are invariably what is currently being used to manufacture MDXX substances these days no matter which pre-precursor is being used,
Again, this is not the put-down that you think it is, and it doesn't strengthen your argument like you think, either.
provided that those that are doing so purify the magical ketone first (so remove what is cleaved off from what is a far more complicated, likely chiral, and frankly “messy” molecule than the more simple safrole or piperonyl precursor that previously the chemist built upon to make the ketone);
There's a lot wrong in this statement, my guy. Firstly, the ketone, MDP-2-P, aka: PMK, is in fact not chiral, and I'm not sure why you think it's more complicated and "messy" compared to safrole/isosafrole. Just because you're intelligent in other fields doesn't mean these giant leaps in logic are sound or accurate.
There's a lot that you say after this that builds on your incorrect assumption that MDP-2-P is chiral (again: it is not), and it would be tedious for everyone involved to call out each of these instances, so we're skipping some stuff here.
The reality of Meh-MDMA is a fact.
That's a weird statement, as there's not much reason to add "meh-DMA" (or my variation on it: "MDM-meh") to the drug lexicon as any rigorous, specific and serious medical / scientific term. It's imprecise and sits as more of an umbrella term for "lackluster drug experiences when one was expecting a full-on MDMA roll." I don't think anyone is seriously claiming that lackluster responses and disappointing experiences when trying to use ecstasy occur sometimes for various reasons. So boldface statements that this phenomenon sometimes happens are not needed and they reflect a misunderstanding of arguments contending that reports of supposed wide-spread "meh-DMA" are exaggerated almost to the point of becoming myth. (Notice I said "almost", guys, before anyone jumps down my throat. I know you had a bad time taking MDMA before. Not saying you didn't. But keep in mind: there are millions and millions of drug users all over the world… what happens in your neck of the woods is not universal to the globe.)
Meh-MDMA is part of the illicit supply of MDMA pills and powders to varying extents all over the world, with no doubt some localities fortunate enough to barely encounter it at all, whereas others might encounter it 90% of the time.
The fact of its existence in the world’s MDMA supply to varying extents cannot be summarily dismissed by the robotic trotting out of “advanced age”, “tolerance”, “set and settling” or “the distinct absence of yellow smiley faces” etc, etc, as sensible explanations.
Again – when this happens, in some instances it's the pill/powder, and in other instances it's the person, or it's a competing medication, or any number of different factors that have been covered on this thread.
All else being equal, the differences must be chemical.
Now if all else were actually equal, that would be sweet. This is not the world we live in though.
Is it one particular chemical that is responsible; likely not.
QED
Is it a group of chemicals with the pharmacological capability, at perhaps very low doses, of inhibiting MDMA’s ability to release that special blend of monoamine neurotransmitters, especially serotonin; maybe.
Likely not.
If this is correct, then does this account for the seemingly subpar quality of modern day mass produced P2P methamphetamine, basically manufactured in the same way but just with different pre-precursors to start with that do not have the methylenedioxy bridge (and tartaric acid resolution to increase the D isomer %), despite us all being told that methamphetamine has supposedly never been so pure and never been so potent, in a similar way to us being told that MDMA pills have never been so pure and dosed so high; I say undoubtedly.
So what you're talking about is first producing P-2-P (phenyl-2-propanone, aka: phenylacetone, aka: benzyl methyl ketone (BMK)), from a starting precursor of something like benzaldehyde, and no that doesn't mean it's some janky move or some crazy amount of extra effort. Then the P-2-P is reduced to racemic methamphetamine in an analogous manner to how MDMA is produced. Since there's no 3,4-methylenedioxy ring present, there are fewer side-product possibilities, FWIW, but no, generally these are two different things being discussed here. You see, the two isomers of racemic methamphetamine are separated using tartaric acid and the unwanted l-isomer is converted into a new portion of racemic meth. This can then be separated again and the process repeated as desired. The purity drives upward with each iteration, so like: 50%, then 75%, then 87.5%, then 93.75%, etc, in theory at least. In practice it's not quite as precise and high-yielding, but you get the picture. Most common meth cuts these days are l-isomer meth or unconverted pseudoephedrine at times when it's produced via reduction of ephedrine/pseudo.
I don’t profess to have all the answers and it frustrates the shit out of me.
I'm sorry to hear you're so frustrated.
But no one can tell me, someone of my experience and knowledge (derived from multiple bases as it has for over two and a half decades), that meh-MDMA, as I’ve explained it, is not a real thing; nor do I subscribe to the defeatist attitude that it is something that is just impossible to scientifically investigate and can never be explained.
It's not defeatist; it's just a fact, unless you can build a time machine to go back and test out the products of yesteryear, this is one of those things in life that we can only guess at and which do no matter any longer as it's in the past and untestable. That's not an opinion in and of itself. Each guess is an opinion, but none of them are verifiable truths.
Ok, I’ll hand over to the naysayers now. I can only hope that those who will inevitably chime in will actually have something constructive to say that they haven’t already said a hundred times already…
Don't I wish. I've been steadfast on my points, and if people take the time to understand what I'm saying, they'll realize that this is a non-issue. No one is arguing what you seem to think they're arguing (i.e.: no one's questioning that these subjective experiences occur, or that impurities exist, or that all products labelled "MDMA" are the same. And it isn't "naysaying"; it's about clarity, using precise definitions, and understanding better the pharmacodynamics involved in MDMA use and how it impacts qualitative experience.