Den enkleste opskrift på krystal Mephedrone

BevItUp

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UWe9o12jkied91d Kan du uddybe den metode, du og mocnykutas diskuterer?

Tak for det
 

UWe9o12jkied91d

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Jeg ved ikke, hvilken procedure han praler med, men lige nu har jeg haft de bedste resultater ved at opløse ketonen i lidt dcm, opvarme lidt til 35-40, tilsætte methylamin på én gang, lade det røre 10 m, som det er, og derefter tilsætte dmso lidt efter lidt i løbet af 20-30 min. vand tilsættes derefter sammen med noget ethylacetat og omrøres et par minutter mere, lad det skille sig ud. fortyndet med kold acetone og udfældet, jeg prøvede både 33 og 37,5 HCl, ingen mærkbar forskel.
Ud af alle de procedurer, jeg fulgte, var denne den reneste og mest udbytterige, og som en sidebemærkning synes jeg, at jo større skalaen er, jo bedre fungerer det.
 

dodobird

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Why add the solvent along with water for flushing though? Noob here 🙏
What uf starting solvent is EA instead of DCM?
 

alwaysalpha

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Dod anyone have tried this recipe???
 

frosties

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Where can I buy benzene/Benzol in Germany anonymously?
 

dnBQByvHb8Zkawbjpx

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Benzen er ret begrænset i EU. Du kan måske finde en sælger, men som individuel forbruger vil du have svært ved at retfærdiggøre køb af mere end en begrænset mængde. Ethylacetat er det opløsningsmiddel til fremstilling af 4MMC, der er lettest at få fat i, det er fuldt lovligt og ikke underlagt restriktioner, og det er ret billigt.
 
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frosties

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Thx I'll go with you his method.
 

dnBQByvHb8Zkawbjpx

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Do you have experience with recovering solvents through distillation? DCM is moderately difficult to obtain (restricted for consumers in the EU) and NMP is expensive, so reusing them could be an interesting option.
 

jango

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dnBQByvHb8Zkawbjpx

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Wow, that yield is massive. Are there any alternatives to NMP to work as a phase transfer catalyst? I've read that it could be substituted by DMSO, are there any other options that may be cheaper and more easily available?

I don't understand why solvents are not reused on a larger scale as well - it limits the volume of waste and brings down the cost.
 
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61-50-7

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Some impurities stay in the solvent so distillation is needed for reuse and it takes a lot of time and need large equipments. For legal businesses it's possible but for drugs way more complicated (time, space, electricity consumption, etc)
 

dnBQByvHb8Zkawbjpx

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I understand that and I had distillation in mind to recover pure solvent. Especially DCM with its boiling temperature of 40 °C requires almost no energy to distill. I'm definitely going to do that and in about a month I should have some first-hand experience to share.
 

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dodobird

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Hi. This post made months of reading confusion go away, very straightforward, thanks @Madre . I had some important doubts to be cleared for upcoming MasterChef tryout ;), appreciate guidance on them. Here we go...

1. Can I replace the benzene with say 300 ml Ethyl acetate. If so what proportion would be ideal and if any procedural changes needbto be made, I am guessing not.

2. Is it Hcl38% we should use?

3.Does the methyl gad need to be relased after animation at all or do we just pour it in shake and then seal to put in the fridge?
How can I reduce this stage to under 1 hour or 2. Any temperature rise monitoring or precaution until this stage? Max temp?

4. Do we need to was the freebase during flushing, with nac03 plus water first and then 2 x with distilled water?

5. Is this method of preparing the 10-90 Acetine hcl38 solution and adding together, better yielding or beneficial over the much common separate addition method of acetone and hcl38? Does it affect quality potency or failure chances or perhaps yield weight of final powder 4mm

6.... Please share equationally correct reagent and chemical quantities for making 10 kg a day. Also any simple apparatus methods for doing this quantity without much labware beside basic flask and jar. What reaction container could I probably use to replace a reactor etc etc


THANKS YOU VERY MUCH IN ADANCE , GREA JOB!!! 😁
 
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