The easiest way to make Amphetamine in the kitchen

OutLaw

Don't buy from me
Resident
Joined
Apr 5, 2022
Messages
5
Reaction score
133
Points
33
Synthesis of phenylnitropropene at home: it couldn't be easier


The main precursor for amphetamine synthesis is phenylnitropropene.
Phenylnitropropene is very easy to synthesize, which makes this method of amphetamine synthesis the most popular among chemists.



The synthesis will require:
  • Flask (glass bottle)​
  • Reflux condenser​
  • Electric stove (for water bath)​

The proportions of the substances are scaled in multiples, but it is recommended not to fill the reactor more than 2/3 of its volume.


The required proportions for a 1L flask are:
  • Benzaldehyde - 200ml.​
  • Nitroethane - 200ml​
  • n-Butylamine - 20 ml​
  • Glacial acetic acid (GAA) - 50 ml​
  • Isopropyl alcohol (IPA)​


The reaction is sensitive to water, so it is desirable to keep the reagents as dry as possible.
Add benzaldehyde, nitroethane, catalyst, and GAA to the flask, stir well, and place on a hotplate. Place over low heat and heat to 60ºC while stirring. You can use a water bath for heating. The temperature in the reactor can be controlled with a thermometer or by touch. The flask should be quite hot to the touch, but there should be no burning of your hand. Cooling is not required for this synthesis, you can simply turn off the heat for a while until the temperature returns to the desired parameters (~60ºC). It is necessary to stir periodically during the reaction, the synthesis time is 3-4 hours. During the reaction, the color changes from light yellow to dark red and remains clear. Then the reaction mixture is cooled to room temperature, poured into a glass or jar, diluted with 250 ml of warm water, covered with a lid and placed in the freezer for 2 hours. When cooled, open the lid and shake gently, allowing fresh air to circulate.

Crystallization occurs rapidly. The jar with crystals is again kept in the freezer for at least 15 minutes. Then you need to break the crystals and wash them with cold water until the traces of vinegar disappear (2...3 times is enough). Then rinse with small amounts of very cold isopropyl alcohol until impurities are removed. The resulting crystals are then dried in the air for a minimum of 10 hours. Store phenylnitropropene in a closed container in the refrigerator or dark, cool place.


Important to know!
  • Flushing with isopropyl alcohol should be performed at the lowest possible temperature. This will reduce losses.​
  • Place isopropyl alcohol in the freezer for 8 hours prior to use.​
  • Rinse until the filtrate becomes colorless.​
  • It is convenient to use an ordinary thin cloth as a filter because the crystals are quite large.​
  • Phenylnitropropene has an unpleasant pungent odor and is corrosive to skin on the hands and face.​
  • The darker the phenylnitropropene, the more impurities it contains.​


Phenylnitropropene can be recrystallized from isopropyl alcohol just before starting the following reaction.
For this purpose, phenylnitropropene crystals are dissolved in isopropyl alcohol at 30ºC and the solution is brought to supersaturation. Then freeze at the lowest possible temperature until crystallization is complete. Filtered when crystallization is complete.
Phenylnitropropene dries in air, It is not hygroscopic (does not absorb water from the air).
Average yield is 300 grams (~70% of theoretical yield).


Watch the phenylnitropropene synthesis video tutorial for a full understanding:
https://bbgate.com/threads/1-phenyl-2-nitropropene-p2np-video-synthesis-from-benzaldehyde-and-nitroethane-henry-reaction.52/




 

Kvadprime

Don't buy from me
New Member
Language
🇷🇺
Joined
Dec 2, 2024
Messages
12
Reaction score
0
Points
1
I have no access to n-Butylamin - but i have aniline (a lot, looooooot). What exits give aromatic amines as a base?
 

Beginner from China

Don't buy from me
Resident
Joined
Feb 14, 2024
Messages
18
Reaction score
2
Points
3
Hi, everybody. I'm from China. My English is very poor. So some translations are not quite accurate. I'm worried about buying the wrong "material". So can anyone tell me the CAS number? I will post the latest list of controlled items below. Please let me know if there are any alternatives. Thanks everyone.
 

Attachments

  • 231BDp8KIb.pdf
    145.9 KB · Views: 994

diegoarmando

Don't buy from me
Member
Joined
Feb 10, 2024
Messages
2
Reaction score
0
Points
1
Hi there,
I'm noob, and watching the other video of amphetamine synthesis i see that is posible to use phosphoric acid to acidificate the product. Has anybody tried to do whith it? I can find 85% phosphoric. If I use it, how many phosphoric will need? 1ml in 10ml of acetone like sulphuric?

Thankyou in advance
 

TucoSalamanca.

Moderator in the Turkish section
Resident
Joined
May 7, 2023
Messages
204
Reaction score
28
Points
28
50% concentration nitric acid 1gr mercury 10ml 50% nitric acid
 

Bitfollow

Don't buy from me
New Member
Joined
Jun 5, 2024
Messages
3
Reaction score
2
Points
3
i am not sure, the result is 3,5g Amphetamin?
 

nobodyname

Don't buy from me
New Member
Joined
Jun 21, 2024
Messages
1
Reaction score
0
Points
1
This might be a dumb question but is this recipe for A-oil?
 

wongivan

Don't buy from me
Resident
Language
🇬🇧
Joined
Jun 7, 2023
Messages
12
Reaction score
6
Points
3
How does amphetamine crystalise transparently?
 

fidelis

Don't buy from me
Resident
Language
🇺🇸
Joined
Mar 1, 2024
Messages
322
Reaction score
402
Points
63
do you mean methamphetamine? here's a link https://bbgate.com/media/methamphetamine-recrystallization.103/
MApjiubht2
 

Kylemalone1297

Don't buy from me
Member
Language
🇺🇸
Joined
Oct 27, 2024
Messages
31
Reaction score
6
Points
8
Can I use naphtha as a solvent for extraction?
 

Kvadprime

Don't buy from me
New Member
Language
🇷🇺
Joined
Dec 2, 2024
Messages
12
Reaction score
0
Points
1
Reading scientific literature two weeks ago came across a patent (it seems like it was a patent, not an article in a chemical journal) about the receipt of an alloy from the metal gallium and aluminum. And this alloy was recommended as a synthesis of hydrogen, instead of using aluminum amalgam. I think so if there is access to metal gallium (yes ... I know that it is very expensive in price, but it is not toxic, more precisely - not very toxic), can easily make a gallium nitrate and make an amalgami aluminum is similar to mercury nitrate. .. wonder if it will work? (translation from another laguage)
 
Top