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Hexanitrobenzene
There is something that really interested me that PHILOU Zrealone mentioned in the trinitrotoluene p ... |
24-10-2002 at 10:29
by: madscientist |
Hexanitrobenzene
I was actually planning on giving 1,2,3,4,5,6-hexanitrobenzene synthesis a try sometime. There's a f ... |
24-10-2002 at 10:00
by: madscientist |
Exotic thermites & analogs
I would think that PbO2/Al mixes would be violently explosive and dangerously unpredictab ... |
20-10-2002 at 19:37
by: madscientist |
Mechanism: N2H4 + NaNO2 ----> NaN3 + 2H2O
It might work - but I'm worried that having such a large quantity of acetic acid present might preve ... |
20-10-2002 at 17:39
by: madscientist |
Diethyl ether
Does anyone have a suggestion as for a good source of diethyl ether? |
20-10-2002 at 17:31
by: madscientist |
Phenol
I suppose benzene might be prepared by pyrolyzing benzoic acid?
If you're looking for aniline, he ... |
20-10-2002 at 17:08
by: madscientist |
Sodium Azide
I don't think gelatine is necessary for preparing hydrazine from urea and calcium hypochlorite. Thes ... |
20-10-2002 at 08:17
by: madscientist |
Phorone
HCl should be soluble in acetone. |
19-10-2002 at 09:05
by: madscientist |
Preparation of elemental phosphorus
It mustn't be too difficult to reduce phosphates with metals - this is what my chemistry book says a ... |
18-10-2002 at 16:45
by: madscientist |
COCl2 from CCl4
Here's a rather interesting reaction that I stumbled upon.
CCl4 + H2O --(FeCl3
18-10-2002 at 13:27
by: madscientist |
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Electrochemical ozone generation
I hear that ozone generators that work by electric discharge in oxygen give poor yields and concentr ... |
18-10-2002 at 13:18
by: madscientist |
Electrochemical ozone generation
I wasn't sure just where this thread would belong, but since the reaction that produces the final pr ... |
18-10-2002 at 12:52
by: madscientist |
Help! I need somebody('s opinion)!
Bombshock is a wasteland of decaying stupidity. Never waste your time with that filth. |
18-10-2002 at 12:34
by: madscientist |
Roguesci is gone
I decided to check for myself - the site really is gone! Everything gives a 403 (access forbidden) e ... |
18-10-2002 at 04:27
by: madscientist |
TO THE MEMBER WHO RECENTLY E-MAILED ME.
You're being paranoid, it's not going to be a FBI agent.  |
17-10-2002 at 19:58
by: madscientist |
Helsinki mall blast
It saddens me to see that we've been visited by rc. Does anyone know what any other internet aliases ... |
15-10-2002 at 15:58
by: madscientist |
Helsinki mall blast
Could you please provide me with some more information on this? I'm startled that he payed attention ... |
15-10-2002 at 13:20
by: madscientist |
Helsinki mall blast
I don't think that "RC" knew about this forum. This forum has remained fairly obscure, and there is ... |
15-10-2002 at 12:22
by: madscientist |
Methyl Ethyl Ketone Peroxide
If the temperature of the reaction is kept low, I suppose HCl could be used.
As for adding the H< ... |
14-10-2002 at 12:13
by: madscientist |
Preparing solid iodine.
The bright red color is due to I3- ions.
I- + I2 ---- ... |
14-10-2002 at 09:13
by: madscientist |
Methyl Ethyl Ketone Peroxide
Maybe they're using a chlorinated hydrocarbon as the solvent, such as CCl2CCl2 ... |
12-10-2002 at 09:37
by: madscientist |
Preparing solid iodine.
Actually, it's not possible to prepare I2 by action of H2SO4 and H< ... |
8-10-2002 at 19:24
by: madscientist |
Phorone
What was the pH of the mix after adding the alkali?
I wouldn't be surprised if the double bonds p ... |
7-10-2002 at 12:48
by: madscientist |
Bringing up old topics is a good thing!
The difficulties I had encountered that Polverone speaks of have to do with heating ammonium oxalate ... |
7-10-2002 at 12:31
by: madscientist |
Phorone
Here's my idea.
Heat HCl and CH3COCH3 together until the solution turns yel ... |
6-10-2002 at 06:43
by: madscientist |
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