LivingOnValium
Bluelighter
@andrewvolcom:
Gongrats for a nice job
.
Hope this will help the people struggling with the OPs.
Gongrats for a nice job

Hope this will help the people struggling with the OPs.
And remember that by removing the excipients instead of extracting the oxy from them, 100% yield is theoretically possible. Anyways, I believe
^Yes, oxy HCl is completely soluble in IPA. The 2nd extraction with IPA is to get rid of anything unnecessary that wasn't removed by the 1st extraction.
In 1st extraction you filter out the gunk dissolved in the non-polar solvent/acetone (and throw it awy) and collect the solid.
Then you perform the second extraction with IPA and filter out the solid (and throw it away) and collect the oxycodone HCl dissolved in IPA.
Then just evap. the IPA and you should get (relatively pure) oxy HCl crystals suitable for smoking or IVing.
Are you serious man? I've been saying this for TWO weeks now.. AND i posted this over THREE times in this thread. Couple of other guys picked up on it and have tried it.. all having great results. Did you just ignore it? or did you happen to not read it?
Jaystyle, good point. The Fda PowerPoint shows 2 out of 4 simple solvent having pretty
good results with physical manipulation and extended room temperature extraction. Plus the fact that the scraping technique being discussed here (pedegg or foot file) created ALOT more surface area than purdue's milling technique. Also jaystyle, notice that simple solvent 3 is missing from the moderate extraction slide, and in the simple extraction slides solvent 3 had the best results. Not by much, but still the best. Now, what would be the reason for doing that? Only thing I
could come up with is it didn't helps to make their abuse resistant claim so they deleted it.