TokinDerrick
Bluelighter
are you serious? if you do that, it won't gel up when one snorts them? like, I could do this with a Teva and snort it just fine?
nky859 said:Thanks for all the replys. I guess im going to just shoot the things up. hahahah
not reaaly just going to parachute.... thanks for info
haribo1 said:The patent I posted was the morphine to hydromorphone patent. You can run it through a translation software. I can't post it here, but it IS all over the net in English
The oxycodone->cinnamyl ester isn't a patent, it's in chemical abstracts in English.
pokergooch said:Im no chemist, but, I believe that codeine is an alkaloid, just like morphine is. Thebaine is what they make oxy and buph out of. oxycodone can be made into oxymorphone, and hydrocodone (which is a product of codeine, I think) can be made into hydromorphone. I dont think that you can make morphine out of oxycodone since the "magic" is Thebaine. I believe that the only wat to get morphine is out of a morphine based drug. Hydrocodone, Oxycodone are semi-synthetic whereas codeine and morphine are 100 percent natural. I may be wrong. but I think im close..
PG
haribo1 said:I never said you could. You can make hydrocodone from codeine. You can hydromorphone from morphine (both easily). The oxycodone cinnamyl ester is something I would make from oxycodone. Yes, you CAN make oxycodone from codeine, but the yields are pitiful. I think 30% is about the max and it's a bitch seperating out the product from the side-products. If you have dihydrocodeine, dihydromorphine is easy but codeine->morphine is a pain in the arse. That 7-8 double-bond means that in hot,acidic conditions, the stuff undergoes the apomorphine rearrangement and turns your product to crap.
haribo1 said:Have you got access to chemical abstracts? The 14-cinnamyl ester is discussed under 'Esters of the 14-hydroxy morphones.' It comes as a PDF so I can't Email/post it & I'm not typing in a 18 page document! Try examining the moleculein 3D, overlaying the etorphine skeleton. Oh, difficult to make the 14-cinnamyl of oxymorphone because the 3 position needs protecting/deprotecting.