Amphetamine synthesis from P2NP via Al/Hg (video)

[Khaafii]

Do you got video of how to create MDMA/XTC?

 

[Mclssmxxl]

Nice, So this is for Speed with purity 70%?

KHaafiiNo, that 70% refers to the yield, meaning 70%(of theory) of your raw material is reduced to your final product.I would wager the unwashed final product is relatively pure, you can test this by weighing your dry, finished product then performing an acetone wash and comparing results.

 

[Khaafii]

No, that 70% refers to the yield, meaning 70%(of theory) of your raw material is reduced to your final product.I would wager the unwashed final product is relatively pure, you can test this by weighing your dry, finished product then performing an acetone wash and comparing results.

MclssmxxlAh okay, by washing the finished product with acetone and then letting it boil or dry? Then what remains is 99% speed, so to speak?

 

[Mclssmxxl]

Ah okay, by washing the finished product with acetone and then letting it boil or dry? Then what remains is 99% speed, so to speak?

KHaafiiSimply dry your finished product, then put it in some filter paper and pour acetone over it.Make sure the whole mass comes into contact with the acetone.Air dry after. This will cause all acetone soluble impurities to dissolve in your acetone, leaving you with somewhat pure amphetamine sulphate.

 

[HIGGS BOSSON]

What is the Büchner measure of the video?

Honolulu98Funnel diameter 200 mm

 

[Khaafii]

Simply dry your finished product, then put it in some filter paper and pour acetone over it.Make sure the whole mass comes into contact with the acetone.Air dry after. This will cause all acetone soluble impurities to dissolve in your acetone, leaving you with somewhat pure amphetamine sulphate.

MclssmxxlSo how much of your endproduct will you lose because of this? percentage wise?

 

[MadHatter]

So how much of your endproduct will you lose because of this? percentage wise?

KHaafii
None, of course. You wash away the IMPURITIES, so you only loose that which is not amphetamine in the first place. What's left is a more pure product.
If you wish you can always cut it afterwards, with non-harmful fillers. But it is important to clean your product from potentially harmful side-products and impurities so that the starting material is as pure as possible. So if you loose some weight in the purification process, its not the product that disappears. Its the junk you dont want.

 

[Honolulu98]

Funnel diameter 200 mm

HIGGS BOSSON

Which of these measures would it be?

 

[Marvin "Popcorn" Sutton]

The Buchner funnel is selected according to its size. It depends on how much of the suspension needs to be filtered at one time.

 

[Honolulu98]

A couple of questions from an inexperienced chemist.

What is the function of the cooling tube (the reflux condenser)? Why is it put?

Is it covered at the top? I don't know how to appreciate it in the video.

What size of these is the right one?

 

[HIGGS BOSSON]

A couple of questions from an inexperienced chemist.

What is the function of the cooling tube (the reflux condenser)? Why is it put?

Is it covered at the top? I don't know how to appreciate it in the video.

What size of these is the right one?

Honolulu98The evaporating gases pass through the condenser are cooled, condensed and returned back to the reaction mixture. It is impossible to close the duct, some gases must come out, so as not to pump pressure. To increase the efficiency of the condenser, you can connect cold running water to it, for this it has two outlets. The larger the size of the condenser, the more efficiently it will work. You can take 4-6-8 balls. It is important that the plume of the condenser fits the flask with which it will connect.

 

[ACAB]

I have a question about the alkalinization,
I have read that one could carry out the neutralization with conventional washing soda, i.e. sodium carbonate Na2CO3, and only then change to NaOH to get to Ph14. This would be cheaper, you can get soda everywhere and it would be more gentle for the product.
Another source, however, says that you should only use NaOH because otherwise the product would be too weak.

Can someone bring clarity into it?

 

[G.Patton]

Another source, however, says that you should only use NaOH because otherwise the product would be too weak.

PennywiseYou can use both ways whatever you want to achieve 14 pH.

 

[megaduck123]

Awesome video! I just got some p2np and almost ready to go, I just need to get some sulfuric acid and some Hg. I am chatting to supplier about some Hg and I have a question for you guys , I can get mercury nitrate and chloride, which should i get ? The chloride is cheaper than the nitrate so i am assumming that would be better but Itll last a lifetime so i really dont mind investing in something better ($45 for chloride and $70 for nitrate).
Also , pure sulfuric acid is not available to public where I am , i think I can get 60% cleaning stuff do you think i could boil/distill this upto a good percentage or should I try harder to buy the 95% stuff?
Also, I have a 5000ml and 2000ml flat bottom conical flask, how much is the max i could run ?
also could i use a glass demijohn (21L or 11.5L) and a ice bath and do 100g runs safely? or would this be hard to work with/not able to handle the exothermic reaction?
Thanks for your time, Happy New Year!

thatfellaHey where did you get P2NP? Do you mind sharing your source, thanks!

 

[HCL]

Do you got video of how to create MDMA/XTC?

KHaafiiThis would be nice.. and very helpful

 

[cyb3r0]

I own these reagents, are they correct and suitable for cooking

 

[HIGGS BOSSON]

I own these reagents, are they correct and suitable for cooking
\\\\These are suitable reagents for synthesis.

 

[diogenes]

The evaporating gases pass through the condenser are cooled, condensed and returned back to the reaction mixture. It is impossible to close the duct, some gases must come out, so as not to pump pressure. To increase the efficiency of the condenser, you can connect cold running water to it, for this it has two outlets. The larger the size of the condenser, the more efficiently it will work. You can take 4-6-8 balls. It is important that the plume of the condenser fits the flask with which it will connect.

HIGGS BOSSONHi, I haven`t got Allihn condenser right now, is it possible to use another type? Or perhaps a fractionating coloumn (this one does not have cooling though). Does it leave to a lot of decrease in effectiveness?

 

[Honolulu98]

Tengo estos reactivos, son correctos y adecuados para cocinar

View attachment 4322

cyb3r0How or where did you buy the sulfuric acid? It would be very interesting. Thank you!

 

[Honolulu98]

Magnesium sulfate at what time is it used?