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Σύνθεση αμφεταμίνης από P2NP μέσω Al/Hg (βίντεο)
- Thread starter HIGGS BOSSON
- Start date
what is the way to check the free base of amphetamine oil -A whether it is good and whether the synthesis was successful
- By Johnny Ringo
First indicator is ph result. Another is the smell and if it converts to sulfate when you add acid you should be fine. If you wash it and filter it I think its pretty safe that even if you fucked up its at least clean shit that doesnt harm you. But I'm no expert I would recommend you text a guy that is in a high position on this site he can tell you for sure.
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- By nofuckups
even with all these, it can be a byproduct salt instead of amphetamine sulfate. These are not good enough signs. Make proper tests after saltifying a batch to ensure it's actually amphetamine. You can try burning it(if it's some byproduct like sodium sulfate, it won't burn with ligher flame(melting point is 800'C+) but amph sulphate would melt/evaporate). Taste can be a good sign too. If soapy or salty, it's likely contaminated. There are various methods to know this but what you described tell nothing much about it.
and some way to check the free base of oil And is it ok? because I prefer to be sure, I do as described and in the video, everything comes out the same, i.e. after adding NaOh two layers separate the top one is yellow ph 11-12 after diluting acetone and sulfuric acid from the first drops flakes form if I reach ph 6 then I have a thick white form like yogurt-cream
Hello everyone, after precipitation from the free base of Amphate sulphate with sulphuric acid to pH 6 I filtered, dried, evaporated the solvent Acetone, the colour remained white, I made a test whether it would burn above 200 degrees, it began to melt and evaporated? I tried the sulphate on the tongue, the taste was very bitter, the smell was delicate, chemical? I took 10 ml of distilled water and threw in about 1-1.5 g of sulphate, I stirred gently and the water was as if I had not thrown anything into it, clean. so it is probably ok? also how can someone advise me in the reaction after adding p2np already, because the temperature will calm down in about 30 minutes, how the colour should be better because in one film it is dark grey and in the other light, Sziwy, does it have any effect on the quality, sorry for my questions, he gave you are obvious and I would like to know for sure that I do not know
Hello, I have a small problem... I only got mercuric nitrate normanal... a volumetric solution... I followed the instructions for dilution exactly... my amalgam reacts and when I add p2np + acetic acid + iso after washing, it reacts very briefly and almost doesn't even heat up... the eccentric reaction lasts about 5 seconds and that's it... do you know what it could be? and one more question... my amphe is always excellent but the yield from 10g p2np is around 3g max, thank you...I follow exactly the procedures from your instructions
hello. after reaction with P2NP+ipa+acetic acid. when I add NaOh and leave it overnight there are two layers on top light yellow oil and at the bottom dark liquid only there are crystals in the bottom layer, as I guess it is sodium sulfate? the question is where could I have made a mistake was the temperature too high after adding P2NP i.e. more than 60 degrees? or if I added NaOH to an even warmer mixture? could I have done something else wrong?