BK-MDMA SYNTHESIS EASY AND FAST METHOD.

Acidosis

Don't buy from me
Resident
Joined
May 31, 2022
Messages
183
Reaction score
119
Points
43
The solution to separate the base of the aqueous layer into cubes is simple, simply use 5-litre hermetic bags and pour the cube directly into the bag and wait for the phase separation, once it has separated the phases the bag was closed and placed so that one of the sides is inclined making the shape of a separating funnel then the tip is cut with scissors allowing a fine stream to come out and you can easily separate the layers
 

cartelloszetas

Don't buy from me
New Member
Joined
Apr 23, 2023
Messages
33
Reaction score
20
Points
8
Feebasse i have on top :)
 

Attachments

  • XJqYo6lL0j.jpeg
    XJqYo6lL0j.jpeg
    4.6 MB · Views: 352
  • aQz2IZCMmi.jpeg
    aQz2IZCMmi.jpeg
    4.4 MB · Views: 381

cartelloszetas

Don't buy from me
New Member
Joined
Apr 23, 2023
Messages
33
Reaction score
20
Points
8
In 2 days made it:)
 

Attachments

  • 8UVL6mX9Zp.jpeg
    8UVL6mX9Zp.jpeg
    6.8 MB · Views: 420
  • D04jdYBx7y.jpeg
    D04jdYBx7y.jpeg
    6.5 MB · Views: 384
  • S5NkQYRi6a.jpeg
    S5NkQYRi6a.jpeg
    4.9 MB · Views: 196

Acidosis

Don't buy from me
Resident
Joined
May 31, 2022
Messages
183
Reaction score
119
Points
43
Looks very nice bro!!..
but from the color of your free base I intuit that it is MMC, correct otherwise the mdmc free base should be Coca-Cola color when dirty and white after a H2O wash with sodium bicarbonate. Likewise, congratulations and I am glad my instructions have served for your success. blessings brother!!.
 

rothschild33

Don't buy from me
Resident
Joined
Oct 17, 2022
Messages
67
Reaction score
44
Points
18
314 gr bkmdma recrystallized using 99% isopropyl alcohol from initial 400 gr bkmdma, total 52190 used: 750g. Acceptable yield for me.

Gonna try recrystallizing again with 1.5 ml water and 1 ml isopropyl alcohol for every 1 gr bkmdma, accidentally added too much HCl initially now it stings when ingesting, might add sodium bicarbonate to the mixture to neutralize excess HCl if 2nd recrystallization doesn't work.

@Acidosis , you're a god


ZxJLoENM3q
 
Last edited:
View previous replies…

chemistry.mob

Don't buy from me
New Member
Joined
Mar 12, 2023
Messages
80
Reaction score
34
Points
18
314 gr bkmdma recrystallized using 99% isopropyl alcohol from initial 400 gr bkmdma, total 52190 used: 750g. Acceptable yield for me.

Gonna try recrystallizing again with 1.5 ml water and 1 ml isopropyl alcohol for every 1 gr bkmdma, accidentally added too much HCl initially now it stings when ingesting, might add sodium bicarbonate to the mixture to neutralize excess HCl if 2nd recrystallization doesn't work.

@Acidosis , you're a god


View attachment 14787
rothschild33May I know from where you bought the precursor 2-Bromo-3',4'-(methylenedioxy)propiophenone and what color and shape did it arrive to you?
and from where did you bought the methylamine 40% aqueous solution (CAS: 74-89-5)?
Thank you!!
 

Acidosis

Don't buy from me
Resident
Joined
May 31, 2022
Messages
183
Reaction score
119
Points
43
314 gr bkmdma recrystallized using 99% isopropyl alcohol from initial 400 gr bkmdma, total 52190 used: 750g. Acceptable yield for me.

Gonna try recrystallizing again with 1.5 ml water and 1 ml isopropyl alcohol for every 1 gr bkmdma, accidentally added too much HCl initially now it stings when ingesting, might add sodium bicarbonate to the mixture to neutralize excess HCl if 2nd recrystallization doesn't work.

@Acidosis , you're a god


View attachment 14787
rothschild33but it should not have any itchiness after recrystallization, I would recrystallize it again in distilled h2o and a mixture of methanol and acetone in the following proportion: for every 1 gram of product add 1 ml of methanol and 1 ml of acetone and 50cl of h20, total 2 '5ml of liquid for each gram of powder, dissolve your mixture well until there are no lumps of powder over low heat and put it in your container and do not move it at all during the course of 4 days so that the crystals form well, if you move the least the container will not crystallize as it should be. blessings bro
 

PokemonGO

Don't buy from me
New Member
Joined
May 15, 2023
Messages
12
Reaction score
6
Points
3
314 gr bkmdma recrystallized using 99% isopropyl alcohol from initial 400 gr bkmdma, total 52190 used: 750g. Acceptable yield for me.

Gonna try recrystallizing again with 1.5 ml water and 1 ml isopropyl alcohol for every 1 gr bkmdma, accidentally added too much HCl initially now it stings when ingesting, might add sodium bicarbonate to the mixture to neutralize excess HCl if 2nd recrystallization doesn't work.

@Acidosis , you're a god


View attachment 14787
rothschild33If u want on dcm heat on 40°C ON 2H you GET 810G POWDER✓
 

antrax

Don't buy from me
Resident
Joined
May 14, 2023
Messages
163
Reaction score
54
Points
28
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.
Acidosis
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.
The precursor of cathinone methylone (CAS
52190-28-0) is 2-Bromo-3',4'-(methylenedioxy)propiophenone? May I know what formulation it has? Most Chinese suppliers sell it in the form of powder and small brown rocks, but I have read in the literature that it is a white crystalline powder.
Methylamine (CAS: 74-89-5) could do the same function as methylamine (40% aqueous solution)?
hydrochloric acid (CAS:
7647-01-0) should be 36% or could it also be used in 37%?
Why is no heat or laboratory equipment used in this chemical synthesis? I'm surprised
And in terms of personal safety, what clothes should I wear to avoid inhaling toxic gases and to prevent chemicals from seeping into my skin and causing burns...?
thank you!! :)
 

Acidosis

Don't buy from me
Resident
Joined
May 31, 2022
Messages
183
Reaction score
119
Points
43
The precursor of cathinone methylone (CAS
52190-28-0) is 2-Bromo-3',4'-(methylenedioxy)propiophenone? May I know what formulation it has? Most Chinese suppliers sell it in the form of powder and small brown rocks, but I have read in the literature that it is a white crystalline powder.
Methylamine (CAS: 74-89-5) could do the same function as methylamine (40% aqueous solution)?
hydrochloric acid (CAS:
7647-01-0) should be 36% or could it also be used in 37%?
Why is no heat or laboratory equipment used in this chemical synthesis? I'm surprised
And in terms of personal safety, what clothes should I wear to avoid inhaling toxic gases and to prevent chemicals from seeping into my skin and causing burns...?
thank you!! :)
antraxyou are correct, all your doubts are as you state, the precursor must be a very dark brown crystalline powder, in reference to methylamine any of the 2 forms will do its job perfectly, simply if you use methylamine HCL it should be go dissolved in water with caustic soda, the hcl to sign the salt at 35-36% is perfect... blessings to the anthrax... c.d.s!!
 
View previous replies…

antrax

Don't buy from me
Resident
Joined
May 14, 2023
Messages
163
Reaction score
54
Points
28
you are correct, all your doubts are as you state, the precursor must be a very dark brown crystalline powder, in reference to methylamine any of the 2 forms will do its job perfectly, simply if you use methylamine HCL it should be go dissolved in water with caustic soda, the hcl to sign the salt at 35-36% is perfect... blessings to the anthrax... c.d.s!!
AcidosisThe precursor should look like this?
8HXuVyWaEx
 

PokemonGO

Don't buy from me
New Member
Joined
May 15, 2023
Messages
12
Reaction score
6
Points
3
what are you laughing at? I ask because I don't know the color it has, and 99% of Chinese chemical suppliers send me a photo as this.
antraxBecause is dirty also sell 2b4m form India the same Brown dirty powder
 

antrax

Don't buy from me
Resident
Joined
May 14, 2023
Messages
163
Reaction score
54
Points
28
Because is dirty also sell 2b4m form India the same Brown dirty powder
PokemonGObut it's actually the original CAS, right? only that it has impurities and that is why the brown color, what color and texture is it in its pure state?
The problem is that all chemical suppliers sell it in the same color (brown) and texture (dusty and with little rocks). I haven't seen any supplier that sells it with a different color.
thank you!! ;)
 

antrax

Don't buy from me
Resident
Joined
May 14, 2023
Messages
163
Reaction score
54
Points
28
Antrax i have in the Next week cas 52910-28-0 with strong quality ready to Europe...any think contact me
AcidosisI do not make payments in advance, only safe payments through alibaba trade assurance or paypal
the synthesis of BK-MDMA that you shared in the forum from where did you get it from?
because I have seen you comment on another chemical synthesis of methylone that another user shared
 

PokemonGO

Don't buy from me
New Member
Joined
May 15, 2023
Messages
12
Reaction score
6
Points
3
I do not make payments in advance, only safe payments through alibaba trade assurance or paypal
the synthesis of BK-MDMA that you shared in the forum from where did you get it from?
because I have seen you comment on another chemical synthesis of methylone that another user shared
antraxIs much more better way made bk mdma and much more pure like he show
 
  • Free product samples

    Testing products from new vendors and manufacturers.

    Get free samples for testing now!

  • Always stay in touch with BB forum. Element/Matrix.

    Connect notifications to always stay in touch with the forum!

    Connect

  • The BB Forum team is looking for cooperation:

    • Traffic arbitrage specialists
    • Spammers
    • Advertising agencies
    • Bloggers/Vloggers
    • TOR sites directories
    • Creative people who can create viral content
    • Administrators of Telegram Channels and Groups

      We will pay more for your traffic than our competitors! $0.1 per visitor!!!If you are interested in, write to the administrator.
Top