Mephedrone (4-MMC) synthesis; easy to perform- high yielding

cartelloszetas

Don't buy from me
New Member
Joined
Apr 23, 2023
Messages
33
Reaction score
28
Points
8
Can made it much more faster and dont need use lab equipment. I see u made for fun if u will need made this way u need pay a lot monay for equipment.
U use also to much chemicals.
When u throw acid your powder need be white milf no like coffie. Of big scale u use too much acetone then and lost a lot of time too wash powder.
U can get 81% powder 75% crystal when u use dcm.
 
View previous replies…

sksameer1

Don't buy from me
New Member
Joined
Jul 25, 2024
Messages
3
Reaction score
0
Points
1
Plse dear explain emijetly fast your recipe....I am waiting here
 

sksameer1

Don't buy from me
New Member
Joined
Jul 25, 2024
Messages
3
Reaction score
0
Points
1
Plse dear explain emijetly fast your recipe....I am waiting here
 

tucoXxX

Don't buy from me
New Member
Joined
Sep 29, 2022
Messages
83
Solutions
2
Reaction score
11
Points
8
I want almost 1 kg of finished product. can I make it 3x the amount of reagents?
 

61-50-7

Don't buy from me
Resident
Language
🇺🇸
Joined
Feb 21, 2023
Messages
34
Reaction score
14
Points
8
better to take x4 : 2Kg of bromoketone, some people don't even reach the 50% yield + if you want it in crystal form, your yield decrease
 

HerrHaber

Don't buy from me
Resident
Language
🇬🇧
Joined
Jan 15, 2023
Messages
576
Reaction score
310
Points
63
I recently achieved a greater than heard of yield of 4MMC hydrochloride in a moment when I expected it the least. Before I make it public to everyone I feel more than just 5 runs are necessary (out of 5, 2 consecutive were high yielding then 2 I thought I would improve but didn't, and another make's the triplicate required for me to state this). However I did run out of stuff and I'm looking forward to completely document this with pictures and all that. And not to be judged for holding back the "precious" information, I can trade off some counterintuitive details of the preparation:

-stirring is key (to keep DCM and water layers in the most intimate contact without phase transfer catalyst)
-relatively long reaction time (about 6 to 8h, I use taking a break by just pause the stirring assuming that if the layers are separate the reaction is almost halted)
-no heat applied (my third and fourth run had average and below yields when gentle heating was applied)
-cooling the mixture and reagents (at the acidification step chilled liquids were the best yielding)
-filter quick (just after the solids precipitate, do not let stay as part of the product will go in solution)

Hope this will help and I promise to be back with details and why not, a validation from another active member.
 
Top