G.Patton

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thanks a lot for the reply I have one more question . what influences the formation of all these pollutants? does the temp also matter? I wonder if the reaction should not be carried out at a temperature of 55-60 degrees ... it seems to me that 80 degrees for 30 minutes causes that so much pollution is formed ...
Mystery_chemistryTemperature and pH have a strong influence on the reaction yield. You have to control temperature as described in the manual. Also, you should carry out acidifying very slowly to save your product. It also can cause side-products formation.
 
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Mystery_chemistry

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Temperature and pH has strong influence on the reaction yield. You have to control temperature as described in the manual. Also, you should carry out acidifying very slowly to save your product. It also can cause side-products formation.
G.Pattonoki then what should the pH be before adding the base? according to the bars, there are 10 in 100% and I even think that more: / even if it goes up to 14, something will happen?

at the temperature won't it be better to keep all reactions in those 55-60? when reducing aluminum amalgam the temperature is so, why are we given a higher temperature here?
 

Bartholomeus

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oki then what should the pH be before adding the base? according to the bars, there are 10 in 100% and I even think that more: / even if it goes up to 14, something will happen?

at the temperature won't it be better to keep all reactions in those 55-60? when reducing aluminum amalgam the temperature is so, why are we given a higher temperature here?
Mystery_chemistry
Do you already have any experience with this reaction?
Or did you already had any success with this reaction?
What was your yield?
 

G.Patton

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according to the bars, there are 10 in 100% and I even think that more: / even if it goes up to 14, something will happen?
Mystery_chemistryIt's okay, pay acidification procedure
at the temperature won't it be better to keep all reactions in those 55-60? when reducing aluminum amalgam the temperature is so, why are we given a higher temperature here?
because here is different reaction, there is no amalgam
 

Mystery_chemistry

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It's okay, pay acidification procedure

because here is different reaction, there is no amalgam
G.PattonI know, but I mean more about p2np which has a melting point of 63-65 degrees ... hence my question whether the reaction at 55 degrees throughout the reaction time will not be a better solution ...
 

Mystery_chemistry

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well ... how to know that everything reacted and the reaction is over? I suggest copper chloride sink to the bottom… a good way out?
 

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chemutil

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If I understand correctly how P2NP is reduced to amphetamine, NaBH4 will reduce the -NO2 group and the alkene group. But I don’t understand what the role of CuCl2 is. Please explain how this mechanism works. Thank you in advance.
 

G.Patton

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But I don’t understand what the role of CuCl2 is. Please explain how this mechanism works. Thank you in advance.
chemutilHi. CuCl2 Works as catalyst in this reaction. Do you need more detailed explanation?
 

Mystery_chemistry

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Hi, I wonder if the reductions can be made on the water only? after alkalisation, pour in a non-polar solvent and pull out the free base. it is possible ?
 

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Hi, I wonder if the reductions can be made on the water only? after alkalisation, pour in a non-polar solvent and pull out the free base. it is possible ?
Mystery_chemistryclick. Steps 1-5 are better in waterless conditions (with one equivalent of NaBH4). After, with the resulting nitropropane and metal chloride as catalyst, water conditions are possible.
 

MisterAnonymous

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click. Steps 1-5 are better in waterless conditions (with one equivalent of NaBH4). After, with the resulting nitropropane and metal chloride as catalyst, water conditions are possible.
William Dampier@William Dampier what is the BP of Amphetamine Freebase and does it need to be distilled under vacuum?
Or does steam distillation also work?
I just want my Freebase colorless like water!
 

KokosDreams

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1- I have a 100L glass reactor and the first cross of the stirrer to move liquid is around 10L that means that less than 10l can't be stirred in my reactor.
btcboss2022
What's the maximum liters of reaction mass you would load into your 100L glass reactor?
 

mithyl2

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is this the correct cas number for the P2NP: 705-60-2

will any other cas numbers work?
 

mithyl2

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and what % Sulfuric acid should be used?
 

KokosDreams

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is this the correct cas number for the P2NP: 705-60-2

will any other cas numbers work?
mithyl2
That is the correct CAS number, I would recommend you to stick to this one.

You can contact Constantylious777 from the forum, he's selling good quality P2NP, also there are other clearnet vendors that offer this product.
 

mithyl2

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That is the correct CAS number, I would recommend you to stick to this one.

You can contact Constantylious777 from the forum, he's selling good quality P2NP, also there are other clearnet vendors that offer this product.
KokosDreamsthanks for letting me know
 

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Hi, have some questions about the synthesis.

6. 25% water solution of NaOH (8 liters) was added to reaction mixture and the phases were separated.

Q: You ad the NaOH to the synthesis and it splits into two laywers, and you drain the bottom layer and keep the upper layer?

7. The aqueous phase was there after extracted with 8 liters of IPA.

Q: I don't understand this part, after separation from step 6 you ad 8l of IPA and mix it?

8. IPA was evaporated on vacuum to an oil.

Q: Can I use a homemade small distiller to evaporate the IPA? And at what temperature should it be evaporated 60C?

9. The oil was dissolved in two liters of acetone.

Q: I don't understand this part, you ad the acetone to the oil and then start with the sulphuric acid step to get it into the right pH?

Bdst regards
 

tucoXxX

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Hi, have some questions about the synthesis.

6. 25% water solution of NaOH (8 liters) was added to reaction mixture and the phases were separated.

Q: You ad the NaOH to the synthesis and it splits into two laywers, and you drain the bottom layer and keep the upper layer?

7. The aqueous phase was there after extracted with 8 liters of IPA.

Q: I don't understand this part, after separation from step 6 you ad 8l of IPA and mix it?

8. IPA was evaporated on vacuum to an oil.

Q: Can I use a homemade small distiller to evaporate the IPA? And at what temperature should it be evaporated 60C?

9. The oil was dissolved in two liters of acetone.

Q: I don't understand this part, you ad the acetone to the oil and then start with the sulphuric acid step to get it into the right pH?

Bdst regards
ImOuthi I am looking for answers to these questions. if you got it, can I see it? I'll go through the thread to see if I can find it.
 

Curiousonion

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Isn't sodium borohydride expensive?
And at 3 kilos to produce 1 liter of amphetamine oil the cost would be a bit too much for it to be attractive.
 

antrax

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Isn't sodium borohydride expensive?
And at 3 kilos to produce 1 liter of amphetamine oil the cost would be a bit too much for it to be attractive.
CuriousonionDid you finally synthesize amphetamine sulfate (speed) following this route?
 
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