BK-MDMA SYNTHESIS EASY AND FAST METHOD.

Acidosis

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Total time to end all process 2hour to form hcl..(the recristalization time have days to create a crystals)
 

bonotuto

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Total time to end all process 2hour to form hcl..(the recristalization time have days to create a crystals)
Acidosiswhere video of it...can you make it and share here...
 

mocnykutas

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Hello, here I attach a simple and simple synthesis of bkmdma with photos of the process and the finished product.
1-To begin with, two plastic drums of approximately 25 liters were brought and inside a drum, an exact 500g of C.A.S: 52190-28-0 of excellent quality was dissolved in 2.5 liters of DCM (dichloromethane) and with an electric drill with a bit mixing concrete was stirred until the complete dissolution of the precursor, this did not take more than a few minutes.

2- now added 1litre of methylamine in in different portions at the rate of 250ml every 10 minutes approximately. At no time was the temperature increase noted since all the reagents were cold before starting, at no time was heat used for this reaction. once all the methylamine was added it was allowed to stir for 40 minutes until no more methylamine gas fumes were observed.

3- 50 minutes after the beginning of the reaction, the agitation was stopped and we waited a few minutes until the 2 layers were separated: the base and and the aqueous layer formed from methylamine and still traces of product, for this another plastic drum was used and the layer The aqueous layer was separated to the new drum for its subsequent extractions of some of the product that remained in the aqueous layer. For this, ethyl acetate was used. 100 milliliters of ethyl acetate were added three times each time to the aqueous layer and it was collected to add it. to the other tambo where the base was reserved.

4- Once the 3 extractions were united with the base in the same drum, the base was cleaned, for this abundant water was added and stirred together with the base and once the water was separated, all the water was emptied from the other drum thus leaving the clean methylone base in the first tube. This cleaning process was repeated at least 3 times until the base did not give off any smell of methylamine. Now a good handful of magnesium sulfate was added to the drum that contained the base and it was left to dry for 20 minutes, during which time it was used to get rid of the cleaning of water deposited in the other bucket. As can be seen, the entire synthesis is being carried out only with the help of 2 plastic buckets and a normal masonry drill with a bit to mix the mortar and cement and with a good source of water near the production area.


5- formation of methylone hydrochloride, for this, sufficient 36% HCL was prepared in a beaker with a little cold acetone, once again the electric drill was turned on and the base was constantly stirred and the hcl was added in small portions and measure the ph until reaching ph 5, at that moment they stopped adding more HCL but the base was kept stirring for a little longer, when we stopped the drill we observed a lot of hydrochloride both floating and on the walls, the bottom of the cube and attached to the drill .


6- filtration process. For this, the other cube was taken again and a filter was placed on top of it, firmly attached with tweezers and all the solution was filtered, leaving the methylone trapped in the filter. The cube and the hole that contained methylone were scraped and drained well. it was ignited and air dried to yield 90% dry of the actual weight of precursor.


7- recristalization . 490g of Methylone HCL were put to recrystallization with water and acetone in the proportion of: for each gram of HCL 1.5ml of distilled water and 1ml of acetone which formed some beautiful crystals and at the same time purified its purity to reach a good percentage of pure bkmdma crystal.
AcidosisHow look freebase
 

Ecko6ap

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Hello, here I attach a simple and simple synthesis of bkmdma with photos of the process and the finished product.
1-To begin with, two plastic drums of approximately 25 liters were brought and inside a drum, an exact 500g of C.A.S: 52190-28-0 of excellent quality was dissolved in 2.5 liters of DCM (dichloromethane) and with an electric drill with a bit mixing concrete was stirred until the complete dissolution of the precursor, this did not take more than a few minutes.

2- now added 1litre of methylamine in in different portions at the rate of 250ml every 10 minutes approximately. At no time was the temperature increase noted since all the reagents were cold before starting, at no time was heat used for this reaction. once all the methylamine was added it was allowed to stir for 40 minutes until no more methylamine gas fumes were observed.

3- 50 minutes after the beginning of the reaction, the agitation was stopped and we waited a few minutes until the 2 layers were separated: the base and and the aqueous layer formed from methylamine and still traces of product, for this another plastic drum was used and the layer The aqueous layer was separated to the new drum for its subsequent extractions of some of the product that remained in the aqueous layer. For this, ethyl acetate was used. 100 milliliters of ethyl acetate were added three times each time to the aqueous layer and it was collected to add it. to the other tambo where the base was reserved.

4- Once the 3 extractions were united with the base in the same drum, the base was cleaned, for this abundant water was added and stirred together with the base and once the water was separated, all the water was emptied from the other drum thus leaving the clean methylone base in the first tube. This cleaning process was repeated at least 3 times until the base did not give off any smell of methylamine. Now a good handful of magnesium sulfate was added to the drum that contained the base and it was left to dry for 20 minutes, during which time it was used to get rid of the cleaning of water deposited in the other bucket. As can be seen, the entire synthesis is being carried out only with the help of 2 plastic buckets and a normal masonry drill with a bit to mix the mortar and cement and with a good source of water near the production area.


5- formation of methylone hydrochloride, for this, sufficient 36% HCL was prepared in a beaker with a little cold acetone, once again the electric drill was turned on and the base was constantly stirred and the hcl was added in small portions and measure the ph until reaching ph 5, at that moment they stopped adding more HCL but the base was kept stirring for a little longer, when we stopped the drill we observed a lot of hydrochloride both floating and on the walls, the bottom of the cube and attached to the drill .


6- filtration process. For this, the other cube was taken again and a filter was placed on top of it, firmly attached with tweezers and all the solution was filtered, leaving the methylone trapped in the filter. The cube and the hole that contained methylone were scraped and drained well. it was ignited and air dried to yield 90% dry of the actual weight of precursor.


7- recristalization . 490g of Methylone HCL were put to recrystallization with water and acetone in the proportion of: for each gram of HCL 1.5ml of distilled water and 1ml of acetone which formed some beautiful crystals and at the same time purified its purity to reach a good percentage of pure bkmdma crystal.
Acidosishow long does the reaction with methylamine take? do I need to close the barrel tightly so that the methylamine does not exhale?
 

Acidosis

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how long does the reaction with methylamine take? do I need to close the barrel tightly so that the methylamine does not exhale?
Ecko6apNo ,the cube is open in all reaction time,dont necessary have close the cube
 

Frit Buchner

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I see China has it cheap. In the us it is $400/g if you can get it. If someone has it in a us warehouse. I know a buyer at a 10 fold markup.
 

mocnykutas

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I see China has it cheap. In the us it is $400/g if you can get it. If someone has it in a us warehouse. I know a buyer at a 10 fold markup.
tropaneIn China they not sell bk mdma because is illigal only some analog eutylone and is shit speed drug. Bk mdma is much more like mdma
 
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Frit Buchner

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Its not the same xD
He use 2broml-3.4methylenodioksypropiophenone
mocnykutasOf course not, not even similar, the similarity ends at the difficulty in obtaining it. I looked up the precursors. I looked up the precursors of the precursors. I can't even buy those legally. All you big shots aught to cut us little guys a break and sell us 5-10 grams of it :)
 

Ecko6ap

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ymaaah

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Why the methylation takes 50 minutes with DCM? Normally with DCM its 2 hours no? and you let the cube open when you do the methylation? Because the methylamine gaz comes out if you dont close the cube
 

Acidosis

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Why the methylation takes 50 minutes with DCM? Normally with DCM its 2 hours no? and you let the cube open when you do the methylation? Because the methylamine gaz comes out if you dont close the cube
ymaaahIf this is another precursor and has neither the times nor the methods for production than other cathinones... but I understand your doubts.
 

Acidosis

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Final process from 500g of 2b3'4mp 390g pure Brown cola crystals of BK-MDMA.
 

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Ecko6ap

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Acidosis

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very similar external to real mdma. what kind of effects? like molly?
Ecko6apYes the original bkmdma is very intense and have very powerfull enthactogen effects,the odor is identical and the effects too.
 

Acidosis

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78%yield...cool!!
 

Cruela

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bonotuto

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please make video tutorial to this step fast method...very usefull if you can do it better than read writing...many of us didnt know well about chemical reagent and etc...
 

K-Cyanide

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I noticed that the precursor is quite expensive (+/- 400 USD)/kg, probably because the demand is nowhere near as high as for e.g. PMK powder. Anyway, has anyone of you guys by chance a reliable source that is cheaper?
 

rothschild33

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I noticed that the precursor is quite expensive (+/- 400 USD)/kg, probably because the demand is nowhere near as high as for e.g. PMK powder. Anyway, has anyone of you guys by chance a reliable source that is cheaper?
K-Cyanide~200 USD/kg from china, source ripping you off or they are just a reseller
 

rothschild33

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Only got methylamine hcl.

Would this work, methylamine hcl dissolved in water then basified with NaOH, then proceed with the reaction?
 
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