|
|
 |
|
|
|
register |
bbs |
search |
rss |
faq |
about
|
|
|
meet up |
add to del.icio.us |
digg it
|
|
|
| Laboratory Tips Safety proceedures, test reagents, drilling rubber stoppers, bending glass tubes, etc. Contributed to by chemists. |
 |
|
|
#1
 2008-12-05, 06:20 |
god_damn 
Regular
|
|
|
|
 levorphanol
anybody ever fuck around with a levorphanol synths?, the synths on DDS seems semi easy.
H is gettoing harder to make, the precursors seem easier for this one, and the potency seems harsh, might be fun to try.
|
|
#2
2008-12-05, 17:30 |
stateofhack
Regular
|
|
|
|
Re: levorphanol
Quote:
|
Originally Posted by god_damn
anybody ever fuck around with a levorphanol synths?, the synths on DDS seems semi easy.
H is gettoing harder to make, the precursors seem easier for this one, and the potency seems harsh, might be fun to try.
|
Heroin is not that hard to make... care to link us up to the synthesis you which to discuss? |
|
#3
2008-12-05, 17:52 |
Von Bass
Regular
|
|
|
|
Re: levorphanol
If only DXM wasn't a stereoisomer :( Otherwise I don't think it wouldn be too hard to remove the methyl & replace with an H on the oxygen.
|
|
#4
2008-12-06, 08:13 |
|
Regular
|
|
Utah: Mountains, Mormons, Meth
|
|
Re: levorphanol
Quote:
|
Originally Posted by Von Bass
If only DXM wasn't a stereoisomer :( Otherwise I don't think it wouldn be too hard to remove the methyl & replace with an H on the oxygen.
|
You'd almost definitely demethylate the N as well, but that's not too difficult to undo. Not that it was viable in the first place. :( |
|
|
|
To the best of our knowledge, the text on this page may be freely reproduced and distributed.
totse.com certificate signatures
|
|
|
About | Community | Bad Ideas | Drugs | Ego | Erotica | Fringe | Society | Technology
|
|
|
|
|
|
![]()
![]()
|
