Hi,
I am posting the process and results of my first experiment to see if any of you smarties have anything to offer. I've read just about every post on here that relates to purification. All in all I think my experiment was a success (while at the same time a failure) but would like feedback.
My buddy purchased two grams but when we got to his house and weighed them on his very expensive scale they each came in at about .785 I'm pissed but what can one expect buying drugs from a fat white chick.. it's our own faults.
1. Dumped the 1.5 grams into a beaker containing 120ml of distilled water
2. Stirred for a while and broke up the clumps but not much dissolved. After 5 mins of continuous stirring and still most of the powder visible I decided to aid it with a tiny bit of heat.
3. Placed the beaker containing the water/coke in a water bath on stove over medium-low heat. Stirred continuously for 15 mins and got the water hot (not even close to boiling but hot) A tiny bit more dissolved but still not much.
At this point I realize that what we have is shit. I'm annoyed but continue on anyway. I was actually thinking there might be zero cocaine in it.
4. Filtered the hot solution but saved the solid material for analysis later
5. Tasted the filtrate (liquid that passed through the filter) and it had a bitter taste and numbed the tongue immediately. Not all hope was lost but I knew we wouldn't get much.
6. Added 10% ammonia hydroxide to the filtrate drop wise every 2-3 mins with vigorous stirring in between. With the first drops, the solution turned a milky/cloudy white. After about 10 mins of stirring and dropping ammonia I noticed some clumps of solid material gathering at the bottom but nothing was clinging to the copper stir rod.
Eventually, after more ammonia was added some gross looking goo was clinging to the rod. I filtered the solution at this point into a fresh beaker and cleaned off the stir rod. The shit that was clumped at the bottom was now caught in the filter and looked exactly the same as the shit on the stir rod.
7. Kept adding more ammonia with more stirring (drop wise of course). Some more clumps formed which we removed. More ammonia and stirring again.
8. Finally i noticed what looked like a small snow storm in the liquid and also realized that the solution was quite clear and not milky anymore. Kept adding more ammonia and more stirring.
9. After awhile a white precipitate was covering the the stir rod. This looked beautiful and glistened under the light. I didn't want to add too much ammonia and over alkalize the solution and ruin it but we didn't have a pH meter or papers handy. I decided to let the solution settle and then add a drop of ammonia to see if anything precipitated when the drop of ammonia hit the solution. It did so we added a bit more and stirred.
10. Now I'm worried that I'll overshoot it and decided to just filter it now. The solid base stayed in the filter but then I added more ammonia to the filtrate to see if anymore would precip out but nothing did.
11. Poured distilled water into the filter to wash the crystals of any ammonia. Did this about 3 times and then removed the filter, pressed it between two paper towels and it is currently drying.
The amount that was left is VERY SMALL. Hardly anything. I can't tell cause it's wet and in the filter but it looks line maybe one line. I don't think it will be worth it to convert it back to hcl.. but I don't smoke so.. I don't know.
Anyway, is there anything here that I did (or didn't do) that may have caused such a low yield or was the shit crap to begin with? Prob crap to begin with but I don't doubt I could have done something better.
Any thoughts would be greatly appreciated.
Thanks
I am posting the process and results of my first experiment to see if any of you smarties have anything to offer. I've read just about every post on here that relates to purification. All in all I think my experiment was a success (while at the same time a failure) but would like feedback.
My buddy purchased two grams but when we got to his house and weighed them on his very expensive scale they each came in at about .785 I'm pissed but what can one expect buying drugs from a fat white chick.. it's our own faults.
1. Dumped the 1.5 grams into a beaker containing 120ml of distilled water
2. Stirred for a while and broke up the clumps but not much dissolved. After 5 mins of continuous stirring and still most of the powder visible I decided to aid it with a tiny bit of heat.
3. Placed the beaker containing the water/coke in a water bath on stove over medium-low heat. Stirred continuously for 15 mins and got the water hot (not even close to boiling but hot) A tiny bit more dissolved but still not much.
At this point I realize that what we have is shit. I'm annoyed but continue on anyway. I was actually thinking there might be zero cocaine in it.
4. Filtered the hot solution but saved the solid material for analysis later
5. Tasted the filtrate (liquid that passed through the filter) and it had a bitter taste and numbed the tongue immediately. Not all hope was lost but I knew we wouldn't get much.
6. Added 10% ammonia hydroxide to the filtrate drop wise every 2-3 mins with vigorous stirring in between. With the first drops, the solution turned a milky/cloudy white. After about 10 mins of stirring and dropping ammonia I noticed some clumps of solid material gathering at the bottom but nothing was clinging to the copper stir rod.
Eventually, after more ammonia was added some gross looking goo was clinging to the rod. I filtered the solution at this point into a fresh beaker and cleaned off the stir rod. The shit that was clumped at the bottom was now caught in the filter and looked exactly the same as the shit on the stir rod.
7. Kept adding more ammonia with more stirring (drop wise of course). Some more clumps formed which we removed. More ammonia and stirring again.
8. Finally i noticed what looked like a small snow storm in the liquid and also realized that the solution was quite clear and not milky anymore. Kept adding more ammonia and more stirring.
9. After awhile a white precipitate was covering the the stir rod. This looked beautiful and glistened under the light. I didn't want to add too much ammonia and over alkalize the solution and ruin it but we didn't have a pH meter or papers handy. I decided to let the solution settle and then add a drop of ammonia to see if anything precipitated when the drop of ammonia hit the solution. It did so we added a bit more and stirred.
10. Now I'm worried that I'll overshoot it and decided to just filter it now. The solid base stayed in the filter but then I added more ammonia to the filtrate to see if anymore would precip out but nothing did.
11. Poured distilled water into the filter to wash the crystals of any ammonia. Did this about 3 times and then removed the filter, pressed it between two paper towels and it is currently drying.
The amount that was left is VERY SMALL. Hardly anything. I can't tell cause it's wet and in the filter but it looks line maybe one line. I don't think it will be worth it to convert it back to hcl.. but I don't smoke so.. I don't know.
Anyway, is there anything here that I did (or didn't do) that may have caused such a low yield or was the shit crap to begin with? Prob crap to begin with but I don't doubt I could have done something better.
Any thoughts would be greatly appreciated.
Thanks