Usually the darker colors I’ve seen (as long as it’s high purity) are caused by using hydrochloric acid addition to precipitate the hydrochloride and overdoing it and then when it dries it turns brown/dark colors. If you know for a fact it’s high purity then all you have to do is turn it back into base dissolve it in some solvent and do some liquid liquid washes then bubble some HCLgas through it and filter the precipitates out and repeat the HCL bubbling process and filtration over and over again until no more precipitous appear
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Yes agree with u, is a real shity , and a hard time to find some good MD here… i think that other Recrystalizations and maybe a little carbon scrub can do the trick for finish the task without do the A/B and washes, and if i need to do it i will precipitate like the old boss shulgin was, ether and a drops of hidrochloric …
I know that marquis test is not acurate but was positive and the rombo shape is a good indicator?
First and foremost under no circumstance carbon scrub the hydrochloride MDMA, you will just end up losing it. Doing it the shulgin way is what got you this nasty looking shit in the first place (if you don’t do it right and you overdo the hydrochloric acid that’s what you get). It’s really easy to make hydrogen chloride gas from sodium chloride ( table salt ) and sulfuric acid. If you don’t know how I can give you instructions how to do it safely and smartly.
Thanks man and i understand what u say, i lost doing this shit, lost a litlle more i dont care another shit, but i think that other crystalization and then other in ipa/acetone and then rex again i will do the trick… i will post then when finish. Maybe do the A/B to the procces for the pills to separate the colorant only for fun and sciens.
Good luck
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You would at least have to do an A/B.
But maybe get it tested, that is definitely the darkest I’ve ever seen mdma
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mi too
Id rather eat a handful of nutmeg…use the gas like the man said…salt (NaCl) and sulfuric acid…I once cut a air tank in half and welded wall half way up then welded it back together. I could pour rock salt (non iadized) in one side and H2S04) in the other and when I was ready to bubble my gas through I’d just roll the tank onto it’s side.
For the small amount he’s doing he doesn’t need anything too complicated all he needs is a 2 neck flask, put salt in it, connect a sep funnel with some sulfuric in it to one of the necks and a hose with which you will direct the gas into a container holding your base mixed with solvent. Make sure the connection to the sep funnel and the connection to the hose are airtight and no leaks occur. Slowly start dripping in the sulfuric on top of the salt and in doing so you will release hydrogen chloride gas that will be forced out of the hose and into your second container holding the solvent plus base.
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gotta add the sulfuric—Dropwise
I miss the good 'ol days and old friends like Strike …you’re not him are u VG?
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Pretty much what I said bro
I think I can safely say I’ve had a very prolific past in very large scale manufacturing and distributing before I went on an extended vacation at Club Fed for it.
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would be funny as shit if VG is Hobart. I doubt it is tho, but IF it is - VG, dm me brehh!
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Nah bro I am not him. If you read enough of my posts and dig enough into old news you might figure out who I am. (I was on CNN every few hours for 2 weeks and in Houston news everyday for 2 months)
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And i believe a newer one is MM2. Its in Europe. Just what i ‘heard’ 
Everybody is somebody!
Yes sir
Have a chemical compound name for this mm2 I have not come across it yet wich is odd for I am pretty up-to-date
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I think the Chinese label their stuff like that
2-MMC maybe? It’s not 4-MMC but it’s much better than I was expecting.
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