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Illicit Drugs & Amateur Chemistry - What to do?
Wake up and smell the coffee. The drug cooks ARE and to a great extent already have ruined things fo ... |
6-4-2007 at 21:25
by: Sauron |
keten lamp
@chemicalpower:
The two stage reaction scheme is a MECHNISM for the overall reaction, not a PROCE ... |
6-4-2007 at 21:17
by: Sauron |
Acetic anhydride preparation
That is perfectly resonable.
It is an extremely rapid process, as I recall, and not a slow evolut ... |
6-4-2007 at 20:57
by: Sauron |
P2P from recycled styrene?
@Nicodem, I have NEVER advocating making weapons of mass destruction on or off this board. To say I ... |
6-4-2007 at 20:47
by: Sauron |
keten lamp
Try reading them AGAIN. |
6-4-2007 at 08:06
by: Sauron |
Illicit Drugs & Amateur Chemistry - What to do?
I find I am utterly disinterested in continuing to participate in a forum where so many members are ... |
6-4-2007 at 08:02
by: Sauron |
Acetic anhydride preparation
No reaction I ever heard of. |
6-4-2007 at 07:49
by: Sauron |
keten lamp
Try reading the posts and you might understand.
I even drew you a diagram.
The reaction is in ... |
6-4-2007 at 02:55
by: Sauron |
P2P from recycled styrene?
Bullshit. He's out to turn this into a meth cook's kaffee klatch, swapping recipes for P2P. And all ... |
6-4-2007 at 02:42
by: Sauron |
P2P from recycled styrene?
All you are doing is wingeing about your criminality being, after all, criminal.
You are not an a ... |
6-4-2007 at 01:51
by: Sauron |
Acetic anhydride preparation
SO2 is not rich dark red-brown. SO2 is colorless. I am well familiar with the smell of SO2 having ma ... |
6-4-2007 at 01:47
by: Sauron |
Illicit Drugs & Amateur Chemistry - What to do?
I suggest, @Tup, that you talk to some coke addicts, heroin addicts and amphetamine addicts before y ... |
6-4-2007 at 01:32
by: Sauron |
keten lamp
I advise that you use conc hydrochloric acid in place of H2SO4
I advise you to distill your VA fi ... |
6-4-2007 at 01:13
by: Sauron |
Acetic anhydride preparation
When I was a teenager I "discovered" a reaction that I have never bothered as an adult to elucidate. ... |
5-4-2007 at 21:58
by: Sauron |
Oxidation of ethanol
For oxidation of ethanol, to acetaldehyde it is useless.
To acetic acid, in inert organic solvent ... |
5-4-2007 at 20:03
by: Sauron |
Oxidation of ethanol
Yes, I noticed that, however it is not an exidation. It is a free radical initiation and dimerizatio ... |
5-4-2007 at 17:45
by: Sauron |
keten lamp
@hector, take heed. Try conc hydrochloric acid instead of sulfuric acid. @chemicalpower said that th ... |
5-4-2007 at 09:59
by: Sauron |
Melzer's reagent & chloral
Get or make trichloroacetic acid.
Reduce it to trichloroacetaldehyde. There are reducing agents t ... |
5-4-2007 at 09:50
by: Sauron |
Acetic anhydride preparation
Try something more inert like petroleum ether or toluene. Look up to double check they won't dissolv ... |
5-4-2007 at 09:35
by: Sauron |
Acetic anhydride preparation
@Per, wash the solid with a solvent that dissolves Ac2O but not NaNO2 or BaOAc. Filter. Then remove ... |
5-4-2007 at 08:47
by: Sauron |
Nitrobenzene
The nitro group being a deactivating one, you will have difficulty chlorinating nitrobenzene. If you ... |
5-4-2007 at 07:20
by: Sauron |
keten lamp
You are right, the patent teaches merely to fractionate off the acetaldehyde formed while refluxing ... |
5-4-2007 at 06:56
by: Sauron |
Acetic anhydride preparation
Did you dry your NO2 as described in Brauser?
Cold trap for gross moisture then PbO2 then P2O5?
... |
5-4-2007 at 06:16
by: Sauron |
keten lamp
Yes I wish I wish I could afford a nice PC-controlled, fully instrumented Teflon spinning band still ... |
5-4-2007 at 06:04
by: Sauron |
Frustrating Chemical
Phloroglucinol if what you mean I think (sym trihydroxybenzene.)
Anyway yes CCl4 can be made from ... |
5-4-2007 at 05:47
by: Sauron |
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