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Sudan azo-compounds synthesis?
What the hell are "Sudan fat-colorants"?
[Edited on 10-11-2004 by Theoretic] |
10-11-2004 at 01:22
by: Theoretic |
Hydrazine
Have a look at E&W (if you don't know about it yet then google explosives & weapons), t ... |
9-11-2004 at 15:24
by: Theoretic |
Trinitrotoluene preparation
I will also post some other preparations of TNT derivatives. I will put all but this one in one file ... |
8-11-2004 at 08:43
by: Theoretic |
Hydrazine
Hydrazine can also be made by reducing nitramine. Nitramine is made by hydrolysis of dinitrourea, th ... |
8-11-2004 at 08:06
by: Theoretic |
Libraries and The Patriot Act
Go to www.fbi.gov, then go to Search, and enter "chemicals". Or just have a look around. F ... |
7-11-2004 at 09:19
by: Theoretic |
calcium amide
"Where does the oxygen go?"
Damn me, what a brain fart.  I mixed up two reactions, ... |
6-11-2004 at 14:18
by: Theoretic |
calcium amide
The old "Preparing alkali amides" thread has several members sharing my viewpoint, also a ... |
5-11-2004 at 13:28
by: Theoretic |
calcium amide
Oh, WHAT?  
"A reaction of CaO with 2NH3 to form Ca(NH2)2 and H2O?"
Not water, bu ... |
5-11-2004 at 07:50
by: Theoretic |
calcium amide
You could probably use calcium oxide instead, this would give you calcium amide and calcium hydroxid ... |
4-11-2004 at 12:30
by: Theoretic |
Trinitrotoluene preparation
Not exactly TNT preparation, but I didn't find a better place to post this...
TNDB - trinitrob ... |
4-11-2004 at 05:56
by: Theoretic |
Help Making Ferric chloride from electrolysis
You could be, in fact, getting a very fine suspension of Cu(OH)2 |
3-11-2004 at 03:37
by: Theoretic |
ethylene glycol -> oxalic acid?
Sorry about that, I myself thought it was improbable the crystals would do mechanical harm, just tha ... |
26-10-2004 at 13:32
by: Theoretic |
My teacher didnt know
Once dimethyl sulfate is inside your body, you wouldn't worry about your DNA methylating and th ... |
24-10-2004 at 11:11
by: Theoretic |
ethylene glycol -> oxalic acid?
So its actual toxic mechanism is, on end, MECHANIC (CaC2O4 crystals)? The crystals actually damage s ... |
24-10-2004 at 10:37
by: Theoretic |
Organic carbon?
I didn't mean Cu(NO3)2 is insoluble, I said that hydrated copper nitrate can be heated to give ... |
22-10-2004 at 13:41
by: Theoretic |
Carbon Tetrachloride CCl4
"Theoretic - sorry but I don't quite see the point.
It's natural for any reaction t ... |
22-10-2004 at 13:26
by: Theoretic |
Organic carbon?
You could get hydrated copper nitrate in this way and then heat it so it decomposes, giving you CuO ... |
21-10-2004 at 12:33
by: Theoretic |
Permanganate
You can react MnO2 (relatively easy to come by) with H2SO4, any concentration. O2 will be evolved an ... |
21-10-2004 at 11:51
by: Theoretic |
Carbon Tetrachloride CCl4
Calcium chloride would eventually predominate in the solid residue from hydrochlorination, the remai ... |
21-10-2004 at 05:31
by: Theoretic |
SUPERBASE! (Well, what is it?)
The hydride ion is a much stronger base than the hydroxide ion. One can deprotonate a water molecule ... |
21-10-2004 at 05:17
by: Theoretic |
Making own Nitric Acid
If you have AN and a distilling setup, but no acid, use a pinch of salt as a catalyst:
5NH4NO3 =& ... |
20-10-2004 at 07:21
by: Theoretic |
Hydroxylamine NH2OH Uses (and Production)
Maybe reacting formic acid with hydroxylamine will give you fulminic acid?
NH2OH + HCOOH => ... |
20-10-2004 at 07:12
by: Theoretic |
Permanganate
Oh, and a good oxidizing agent to make the manganate is NH4NO3. It leaves no nonvolatile residue, so ... |
20-10-2004 at 06:48
by: Theoretic |
Dichloromethane from methanol?
Dehydrogenating methanol to formaldehyde, then reacting it with SOCl2 (not PCl5) is a viable method, ... |
20-10-2004 at 06:36
by: Theoretic |
Aluminum powder synthesis
Sodium will reduce AlCl3 just fine, anyway your calculations show it.
I read somewhere in this foru ... |
20-10-2004 at 04:46
by: Theoretic |
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