TsarTsar444
Asexual peaceful balkan monk
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First of all you need to have a cooled down mixture composing of a random amount of 2 ingredients, lets say for our examples 34g of 30% H2O2 and 150g of 80% HCO2H. Then you basically just need to add 32g isofrafole desolved in acetone slowly with droplets into this mixture and stir the whole time so that the temperature DOESN'T exceed 40°C (trust me boyos, i almost died from this the first time i did it because i was watching Netflix). The pouring of the acetone is like 1 hour and you can use some external cooling device to help it not exceed 40°C. The steering however is like 12-16 hours (i personally did it the whole day 16 hours because i have OCD and ADHD so just to be sure 
). For a cooling device you can use like an external bath, the water will help it not exceed 40 degrees. During these 16 hours the solution should go from an orange to a deep red color. Then you remove the excess acetone and you should get about 60g of residue. You dissolve this in 60ml methyl alcohol and then that mixture treat it with 360ml 15% H2SO4. Heat this mixture for 3 hours in a hot bath. After it cools then use dyethil ether or benzene (this is the only thing i found in my university laboratory in the Balkans but the first one is more ideal). Then you should wash this solution with normal water and after with diluted NaOH. Then with filtering you should get like this powder constitution around 20g 3,4-methylenedioxyphenylacetone. Idealy you csn use a water pump at 160°C to distile it further to get a more pure product (this is obviously hard to obtain and i didn't have it either). Then add this to 65g formamide and heat for 5 hours at 190°C. Cool it and then add 100ml water, then use benzene for extracting it and then evaporate the compounds with a vaccum to get the residue. Add 8ml methanol to this residue and 75ml 15% HCL, heat for 2 hours on bath and then with vaccum extract the residue again (yeah there are shiton of steps with countless of residues but it just sounds intimidating, trust me its easy once you get used to it). The end residue you get should be around 11-12g of MDMA.
(FBI i only used this personally, never sold it to anybody, so keep coping for me)
). For a cooling device you can use like an external bath, the water will help it not exceed 40 degrees. During these 16 hours the solution should go from an orange to a deep red color. Then you remove the excess acetone and you should get about 60g of residue. You dissolve this in 60ml methyl alcohol and then that mixture treat it with 360ml 15% H2SO4. Heat this mixture for 3 hours in a hot bath. After it cools then use dyethil ether or benzene (this is the only thing i found in my university laboratory in the Balkans but the first one is more ideal). Then you should wash this solution with normal water and after with diluted NaOH. Then with filtering you should get like this powder constitution around 20g 3,4-methylenedioxyphenylacetone. Idealy you csn use a water pump at 160°C to distile it further to get a more pure product (this is obviously hard to obtain and i didn't have it either). Then add this to 65g formamide and heat for 5 hours at 190°C. Cool it and then add 100ml water, then use benzene for extracting it and then evaporate the compounds with a vaccum to get the residue. Add 8ml methanol to this residue and 75ml 15% HCL, heat for 2 hours on bath and then with vaccum extract the residue again (yeah there are shiton of steps with countless of residues but it just sounds intimidating, trust me its easy once you get used to it). The end residue you get should be around 11-12g of MDMA. (FBI i only used this personally, never sold it to anybody, so keep coping for me)
