• Psychedelic Drugs Welcome Guest
    View threads about
    Posting RulesBluelight Rules
    PD's Best Threads Index
    Social ThreadSupport Bluelight
    Psychedelic Beginner's FAQ
  • PD Moderators: Esperighanto | JackARoe | Cheshire_Kat

mCPP,mMPP,pMPP,methBZP - piperazines

> I feel its a price you have to pay if you truly
> want to research theese drugs. No one said it was
> going to be an easy ride.
Sure, there is a price to pay for research...
But what end is this research for? Is this just some sort of academic masturbation for pharmgeeks, or is it just a convenient excuse to get fucked up on exotic drugs? I'm sure for some people that's the case, however, I'd like to think most of us are/were in it for a higher purpose... The end goal here is not to research just for the hell of it, but to discover the good ones and weed out the second rate or worse ones. The goal is to find new psychedelics that can be declared ready for prime time some day... to find new tools for the psychotherapist and new entheogens for the shaman. The goal is to do enough research that they can either cease to be research chemicals and become mainstream drugs... or to find out if the drugs are duds that should just be kept frozen in the lab as reference samples.
Many research chemicals aren't going to turn out to make the cut. They're going to have too many problems... high levels of negative side effects, questionable or bad safety profiles, insufficient levels positive effects to be worthwhile, unpredictability, etc. What matters here isn't what individual people get out of them, but how it plays out in large groups. It doesn't matter if 5 or 6 people have great experiences with XYZ, if the other 94 or 95 people are having convulsions and blasting diarrhea and vomit all over the room. If those 5 or 6 researchers wanna keep using it, that's their call... but if most users react badly (or at least, not goodly enough) then the drug should probably be written off as "not ready for prime time" and crossed off the list of things worth researching.
Personally, I had some good times with 5-MeO-DIPT, for example. The only downside for me was diarrhea about half of the times. The problem though is that I didn't think it had very much to offer except perhaps as a recreational substance. It has *some* deeper potential, but not a whole lot. It probably wouldn't be too effective on the shrink's couch, and I can think of much better entheogens. Combine the small return with the diarrhea and the percentage of people who find it unpleasant, and I think you've got the makings of a little bit of a dud. There's chemicals with much more potential that DON'T make you pay the price, so why waste too much effort on it?
Anyhow, the fact that some people like some research chemical or another isn't the point here... Research chemicals not only need to be used with a different approach from standard drugs, they also need to be rated with a different approach. I'm rating these drugs not based so much on my personal experiences as on the way the whole user population reacts. What are the average trends? Think of research chemical users as the filter between the lab and the streets, which filters out the drugs not suited for general public audiences. We're sort of like the FDA of the psychedelic scene... we offer up our own bodies as lab rats to test new substances to make sure they're safe, effective, and not unduly unpleasant.
To try and take this back to the original topic... I don't think the piperazines really make the cut. My personal experiences with BZP, TFMPP and mCPP were very negative. I've heard many other negative reports, similar to and different from my experiences. The negative reports far outweigh the positive ones... and even the positive ones I've gotten have mostly been weak - stuff like "It didn't suck but I'd rather do meth" or "It was vaguely like MDMA which was interesting, but that headache..."
We even have some real clinical data on the piperazines. I've got a stack of over 100 pages of scientific journal articles on piperazines. These include the results of human tests on quite a few folks. The results aren't too pretty... especially mCPP, which earned the classification "panicogen" in two of the articles.
There hasn't been very much in the way of safety profiling... I don't know of any confirmed deaths so far, though there have been rumors. They certainly don't FEEL very safe, though that's not a very solid argument. They produced some very disturbing physical symptoms for me and others, and the fact that the stuff can give people pounding headaches and a flu-like sensation for 2 days.... that really doesn't give me the warm fuzzies about the safety of the piperazines.
All in all, this group of drugs doesn't really seem to make the grade as far as things I'd want to see being used by the general public. If you like them and don't mind the risk, I certainly won't stop you... but I really don't think these are substances that ought to be recommended to people.
 
I have to agree with Murple in regards to the use of these research chemicals. I believe that they purely a novelty, that just as much, if not more can be gained from using the more traditional psychedelics.
It is however possible that through this search for new experience, that we bump into a compound or tool that can be used in a context not initially intended or expected. This is where controlled experimentation sometimes falls short. In an uncontrolled environment people experiment in a much greater variety of situations and times.
All of the currently avialable research chemicals have provided various people with wonderous experiences, while other have had a negative reaction to them. This is where psychedelic experience is also subjective. I cannot really put one chemical over another as it is only in my experience that I can judge the value of these compounds.
The consensus does seem to be similar in regards to the prefrences of coumpounds.
2ct7 - Variable positive reaction, body load usually outwieghs the insight.
2ci - Positive reaction. Great and in depth experience with little body load.
AMT - Overwhelming experience. Mixed positive and negative reactions. Is it really worth it view seems prevalent.
MBDB - Novelty, not worth while seems the general opinion.
Methylone - Ketone analog of MDMA - Same as above. In general there are few compounds of the MD family of compounds that have the same magic as MDA and MDMA.
4-(HO/Acetoxy)-DIPT - General view that it is not worth the body load. Some positive, mostly negative. Does not weigh up against the traditional psychedlic.
4-HO-DET - Could be the next big thing is psychedelics. Not as heavy or dark as 4-HO-DMT, general opinion is that this is a carefree compound with much room to move. Hopefull for future development. Psychedelic Mood enhancer?
5-MEO-DMT - The spark of DMT from a different angle. This one truly sits up there with the great ones like DMT. A few negative reactions. Similar view as DMT, though perhaps even more positive.
TMA's - In general a not worth while point of view. Physical outweighs the not so unique positive effects that can be acheived on other compounds.
Piperazines - General consensus is that these compounds offer too little over the positive. Stick with the traditional stimulants.
DPT - Similar in intensity to DMT. General view is that it is quite unique and distinct in the state of mind you enter. Not so many positive reactions. Is it worthwhile? Not as amazing as DMT people have noted.
DIPT - Unique effect, not for recreational use seems the general opinion. Novelty experience?
Other compounds out there that could be promising but have too little research to base an opinion on include:
TMA-6
2C-E
2C-G's - These could be interesting.
It will be interesting what the next big thing will be. ;)
 
> AMT - Overwhelming experience.
Many people report the exact opposite.
> 4-(HO/Acetoxy)-DIPT - General view that it is not
> worth the body load. Some positive, mostly
> negative. Does not weigh up against the
> traditional psychedlic.
I don't know what you're basing this on... I haven't tried either of the acetoxy compounds, but the general consensus I've found is that most people find that 4-AcO-DIPT, 4-AcO-DET and psilocybin are so similar they'd have a hard time telling them apart. There's some subtle differences which make some people have a slight preference for one of them, but most formal reports and most people I've talked to seem to indicate that these are very similar. In fact, based on your summary, I have to wonder if you might not be confusing 4-AcO-DIPT with 5-MeO-DIPT.
> 5-MEO-DMT - The spark of DMT from a different
> angle.
Not really... most people who've tried both (myself included) find that DMT and 5-MeO-DMT are very distinct... DMT has much more in common with DPT, psilocybin or LSD than with 5-MeO-DMT. 5-MeO-DMT is very intense and its a short trip, but qualitatively it's kind of an oddball member of the tryptamine family.
> TMA's - In general a not worth while point of
> view.
I haven't seen enough reports to draw any real conclusions yet. I've seen a few people describe TMA-2 as a little boring, but I haven't heard anything actively bad about it.
> DPT - Similar in intensity to DMT. General view
> is that it is quite unique and distinct in the
> state of mind you enter. Not so many positive
> reactions.
DPT really shouldn't be compared to DMT. As with 5-MeO-DMT, because of its chemistry, people expect it to be a DMT-alike. It's really not. It can get quite intense when smoked, but not as intense as DMT. And taken orally or snorted, its really more along the lines of LSD or psilocybin. Also, I've heard of way more positive reactions than negative... and most of the negative reactions I've heard have been related to physical discomfort from snorting it. DPT has been clinically studied in humans as a psychotherapeutic tool with quite good results (Spring Grove Hospital in the 1970s, treating alcoholics and terminal cancer patients).
Your other analyses are similar to my conclusions... but I'm really wondering where you got the data for making the conclusions I quoted above. The 4-AcO-DIPT summary you made seems especially off-base, and I'm curious if maybe you did confuse it with 5-MeO-DIPT...
 
The only thing Im really getting from reading all this is that these chemicals seem to effect you all very differently.
I for example find AMT to be useful, whereas Murple does not.
Its all a matter of opinion and what works for you. There is no need to argue about which is better. Especially since youll never come to final answer on the best since you all have your own opinions.
 
You're missing the point... when rating these research chemicals, individual opinions mean diddlyfuck. It doesn't matter that you like AMT or that I don't... what matters is when there's a statistically significant number of people who have used it and reported on it, you add up the good and the bad (giving extra weight to bad effects that involve physical danger) and see what the average results are. What drug is better or worse for YOU is a matter of personal opinion... but what determines which are better or worse in the bigger picture is a little less vague. A drug that has a clean safety record is better than one with lots of ER visits and a few deaths. A drug where 10% of people report nausea or headaches is better than one where 70% of people report puking.
Basically, if someone who has never taken a certain drug before can know that approximately 75% of users have good results with no downsides, that drug is "better" than a drug where only 50% of the people have had good results. The fewer people who have bad reactions to a given drug, the less chance YOU will have a bad reaction to it... therefore, it's a better drug, because you've got better chances of having good results. Maybe once you actually try the drug you'll find that you're in the 25% chance that does react bad, that means its not a good drug FOR YOU... which is an entirely different thing. The drug is still on the whole a better drug since its better for more people.
A drug which produces more good effects and less bad effects for the greater number of people is better than any drugs with less positive numbers.
 
Originally posted by Murple:
I've found is that most people find that 4-AcO-DIPT, 4-AcO-DET and psilocybin are so similar they'd have a hard time telling them apart. There's some subtle differences which make some people have a slight preference for one of them, but most formal reports and most people I've talked to seem to indicate that these are very similar.
I have yet to try 4-AcO-DIPT, but I don't think 4-AcO-DET is so mushroom-like that I would have trouble telling the difference. Despite the simple duration difference, (4-AcO-DET lasts 1/2 as long as mushrooms) they each have their own distinct feel to them. Very subtle though, difficult to discern.
Not really... most people who've tried both (myself included) find that DMT and 5-MeO-DMT are very distinct... DMT has much more in common with DPT, psilocybin or LSD than with 5-MeO-DMT.
I agree, DMT and 5-MeO-DMT do have their own distinctions, but I think they are more similar to each other than DMT is to psilocybin or LSD. I don't think the two are really very similar at all though. I think a lot of people say DMT is like a 5 minute LSD trip simply for lack of a better way to describe this unique psychedelic.
DPT really shouldn't be compared to DMT. It can get quite intense when smoked, but not as intense as DMT.
Again, I agree that the two should not be compared. I must disagree with this, however, and say that DPT can be just as intense as DMT if taken IM, and lasts much longer. They seem to have a similar feel to them too, very primordial.
Since the floor was opened...
Methylone is incredible. For me, it is very opening and introspective, just as nice as MDMA if I had to compare the two. Each definitely have their own nuances, which show themselves to the experienced user. But I think both would make excellent therapeutic tools.
I enjoyed 2C-T-2, but not enough to take it at a low dosage again. I think if I were going to bother with this one again, it would be at a more heroic dose for a really intense experience. Otherwise, I prefer 2C-I - then 2C-T-7. But I experienced something different with each 2C that I've tried, and like them all for different reasons. I'm really excited to learn more about 2C-E though, and can't wait to try 2C-B.
 
Murple:
My appologies, I meant 5-MeO-DIPT. I think I did an accidental copy-paste of the wrong name.
:)
Since the analysis was quite quick I made a few mistakes.
In regards to 5-MeO-DIPT the definition of spark was intensity. In regards to intensity and duration. Qualitively they are quite distinct, I agree.
Have not tried the TMA's either. The report was a quick analysis to try and establish the favourability of each compound. The TMA's had few favourable conclusions with exception of Shulgin's reports.
I based all my conclusions on most of the Erowid reports, Pihkal, Tihkal. A number of research papers, a few other books by various authors. Lycaeum Leda trip reports. Bluelight trip reports and personal experience.
:)
Thanks for the input though. I should refine the ideas however, it was a bit of a 5 seconds job.
 
SovietContin said:
Quite simply, [Murple]'s objective when he uses drugs and doesn't simply like things because others do.
ROFL! You are joking, right? This is one of the most ludicrous (and ironic) comments I've ever read on this site.
What bothers me about Murple is this: despite claiming (at least just now) that he likes some drugs, the VAST majority of his posts are NEGATIVE. I rarely if ever see a post by him that is praising a drug...rather, he is always bashing on some drug (or someone). He is one big ball of negativity.
Furthermore, opinions CAN'T be wrong, by definition. I think heroin is a shitty drug -- it does nothing for me whatsoever -- yet I don't go around calling heroin users morons. Murple, why do you feel this need to constantly criticize and patronize others? Is that really the only thing that gives you any satisfaction?
 
this is a really good thread with some good information from trusted individuals, lets not start murple bashing or belitting each other and get it locked.
anyhow i'd have to agree with the overall concensus that though these rchems are popular that doesn't necassirly mean they're all gems. personally i see more promise in the PEA's that are on the market compared to the trypts. i feel that 2c-i could easily become a great pyschedelic for the whole community if it ever got to that level. it has minimal body load, great introspectiveness, a very clean feeling, gentle comedown, and little to no hangover at all.
it seems that the 2c* family has much to offer, including 2c-c, 2c-e, 2ct4, 2c-g. and also the analogs that are already out there like DOB.
 
Murple - I would like to commend you and the others that have participated in this post and creating one of the most socially relevent posts that I've ever read on Bluelight.
Murple really is embracing what this website and this community is SUPPOSED to be doing. "Harm reduction" is something that I really think Bluelight lacks sometimes. It's easy to go into Psychoactives for Beginners and ask what people do to "blow up" while they're taking MD**. And frankly, I think there should be a new forum for these kinds of things called "Drugs for people who don't give a fuck." Hell, we could even start a new website; I'm sure that www.getfuckeduprealgood.com is probably even available.
This site is supposed to be about people watching out for people, helping them where we have failed in the past, and hopefully imparting the same kinds of wisdom along the way. I know even SovietContin, in his own way, knows that he's helping people, albeit belittling them (mostly) along the way. That's why he's on here, I think. That's why I get on Bluelight. I mean, I'd love to know how to twirl PhotonLights in the figure-8 so that I can trip out some 16 year-old KandE raver, but that's not what this place is about. Or, at least, not what I think/want it to be about.
And frankly, this conversation gets to the root of the problem. There is a HUGE difference between what CAN be and what SHOULD be. Jesse Ventura CAN be the Governor of Minnesota, but SHOULD he be? Drano CAN be injected but SHOULD it be?
Now mind you, I have no intent on taking away personal freedom, so if you want to inject 200mg of AMT into your eyeball, then so be it. But, there is just not enough information about some of these things to make an informed decision about whether or not they should be available. Whether illicitly or not. Most drugs that people would consider mainstream are things that have extensive profiles written about them, we know what MOST of the contraindications are, etc. And most of these have very little immediate risk associated with them. And as for long-term risk, we're all adults (or should be, at least), and we poison our bodies and accept that. Of course, we may not know some of the ways that we poison ourselves yet, but that is part of the implicit risk that you take when you imbibe.
Just because people HAVE taken these chemicals, doesn't mean that they SHOULD, or that because they were able to "enjoy" the experience, that it is safe or good for you. There just isn't enough research. Even the ones that Murple labels good, although there has been some research, it may not be enough. We'd like to think of ourselves as "psychedelic pioneers," trying out the "drugs of the future," but really, MOST of us aren't. Even our beloved Dr. Shulgin isn't doing what I think is good for this community. The people that I think do the best things for our community are the people out there finding out the LD50 of 2,4-whateveramide, performing the 1st level trials of these and other drugs; not finding out that "The lovemaking was phenomenal, passionate, ecstatic, lyric, animal, loving, tender, sublime" on 2C-B. Hell, that's why most uninformed people take 5-MeO-DiPT.
And the sad part of this, is that I know I want to try 2C-I, and I know I would in a heartbeat if it was offered to me and I was sure that's what it was. But, am I going to be another happy customer, or am I going to be another Danielle Heard?
 
The main goal, as murple stated, is to move these drugs from research chemicals to trusted, common chemicals. That will, I'm afraid to say, take quite some time.
 
> The people that I think do the best things for our > community are the people out there finding out the
> LD50 of 2,4-whateveramide, performing the 1st
> level trials of these and other drugs; not finding
> out that "The lovemaking was phenomenal,
> passionate, ecstatic, lyric, animal, loving,
> tender, sublime" on 2C-B.
You are right and you are wrong.
Yes, the people who are really doing useful things are the ones doing safety tests, receptor binding profiling, and all that good shit.
However... the people like Shulgin are the ones who are designing the stuff and doing initial trials. If something gives you a headache and makes you puke for 3 hours all for just a few tiny trails... does it really matter if its safe? Who's going to want to use it anyway?
I think theres several stages here that things need to go through. Once a chemical is designed and made, it needs to be tested by a small circle of people. If it shows promise, enlarge the testing circle. If it still shows promise, get it tested for safety and all that. If it passes all that, excellent.
 
I've gotta ask - am I like the ONLY one who doesn't find 2C-I all that special? I've taken it maybe 25 times in doss from 5-35mg orally, snorted it, and smoked the freebase - it's smooth, pleasant, friendly, and maneagable sure, but lacks (to me) any sort of depth, sparkle, and visuals that make both T-2 and T-7 so awesome (to me)
That 4-AcO-DET however is completely fascinating (to me) - I ate 30+ mg one time and was beseiged by chirping and music playing computer-entities from a higher dimension(which freaked me out pretty bad [even tho they were "communicated that they loved me!] and the trip was aborted via high-dose benzo).. A great chemical, too bad it's so hard to make and so unstable afterward :(
As for shallow recreational slop like 5-Meo-DiPT - yea it may not be the marvelous psychedelic like LSD or whatever, but that might not be it's niche!! Maybe it's a good low dose thing for bored yuppie couples who aren't having sex anymore becuase they drink too much and spend all their time questing after new cars and houses??
These chemicals have immense UTILITY, some just not so much so for psychonaut types...
 
Heh... somehow I don't think too many yuppies will be into something that has them glued to a toilet for a few hours blasting liquiturds out their asses.
 
Originally posted by Murple:
Heh... somehow I don't think too many yuppies will be into something that has them glued to a toilet for a few hours blasting liquiturds out their asses.
Liquiturds! Hahaha. Murple, you are too much.
 
Top