Metode til oprensning af MDMA/ecstasy

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Hej venner, tak for bidraget, det fungerer meget godt, men jeg er i tvivl, når jeg krystalliserer (krystaller udfældes meget meget godt), får jeg ikke krystaller som de typiske af mdma, det er noget mere svarende til snefnug, til isfrost i et glas på en snedækket dag, det er glas, men meget skrøbeligt. Hvorfor kan jeg ikke få stærkt glas? Tak og mange hilsner 😊
 

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Hej, det var så lidt! Bruger du et køleskab til krystalliseringsproceduren? Jo hurtigere nedkøling, jo mindre krystaller.
 
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Ja, selvfølgelig, først lader jeg det stå ude, indtil det har stuetemperatur, så er 15 eller 20 % allerede krystalliseret, så sætter jeg det i køleskabet i 2 timer og derefter i fryseren i 3 timer. Næsten 100 % af det vaskede produkt krystalliserer, men krystallerne er meget skrøbelige, og når de håndteres til emballering, bliver de til sand.
 

Mr Good Cat

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Jeg har lavet IPA et par gange, og jeg gætter på, at denne "sand"-krystalstil er en naturlig egenskab ved IPA-krystallisering. Prøv at omkrystallisere den i vand for at få store bjergkrystaller.
 
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Mr Good Cat

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Jeg har bemærket, at IPA er godt til at fjerne klæbrige, sorte forbindelser, som er sideprodukter af syntese.
 

William Dampier

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Large crystals are obtained with the inclusion of a water molecule. Therefore, sometimes it is better to use aq. HCl acid or add water additionally. You must begin crystallization at room temperature so that the process does not begin quickly. If you show a photo of your crystals, maybe I will tell you that you can change for this and get it in a larger size.
 

Keychainsaw

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I read heat makes it brown in here,
I had some issues with the hobby project. The sirup smelled like methylamine in the glass tray and im afraid there might be some methylamine hcl in the end product. Either way this looks fucked up and it looks like it doesnt want to dry any further. Acetone wash just usually turns it into a black tar. Have to say i forgot to dry it does the 4% aq make a bid difference?

This is what i managed to scrape together and kind of dry out. It tastes more salty than bitter. I dont know how methylamine hcl tastes but drying in the oven doesn't make it appear dryer. Its more tarlike than anything else. I'm ready to give up and just flush it. I did manage to get a whiter one with acetone wash but it has the same non bitter taste. Slightly salty. Could other salts have formed in the process? Maybe the aq layer was pipetted up aswell, in that case it might contain trace amounts of mercury?
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G.Patton

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Have you dried this in an oven? At what temp? I assume, there are not a lot of MDMA in this "product".
Looks looks dog shit.
 

Keychainsaw

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105 Celcius. I did manage to get a few gr of good stuff out it before with acetone washes it yielded only a few gr. Thanks for confirming to toss it than i stop wasting and experimenting on it. To be honest the taste test did not pass and it tasted salty and slightly metallic. It didnt want to dry or crash i will simply dump it. Thanks for the fast reply.
 
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