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Dinitrotyrosine
The salts of 3,5-Dinitrotyrosine itself don't loolk to be of great interest, or at least of no great ... |
29-5-2008 at 01:32
by: Axt |
shock sensitive mixtures containing k-chlorate
Seems a bit farcical for someone to try pass a patent for armstrongs mix just last year, but anyway. ... |
26-5-2008 at 23:11
by: Axt |
h202 concentration?
An interesting patent, pitty its jap. It seems its just an acid stabalised H2O2, though it would be ... |
26-5-2008 at 06:26
by: Axt |
chlorine azide
If your book didnt contain references, this is the original preparation which uses acetic acid in pl ... |
25-5-2008 at 12:30
by: Axt |
5-ATZ(5-Aminotetrazole), the nitrotetrazolate ion and friends
[quote][i]Originally posted by The_Davster[/i]
dichloroglyoxime was used instead of glyoxime, as it ... |
23-5-2008 at 16:16
by: Axt |
Glyoxime, Diaminofurazan and Some Energetic Derivatives
Heres one you may be interested in Engager, noting your post in "Announcements of Articles in Progre ... |
23-5-2008 at 15:28
by: Axt |
Trinitrotoluene preparation
<b>Preparation of explosive substances in the laboratory. II. Preparation of trinitrotolu ... |
23-5-2008 at 13:44
by: Axt |
2,3,5,6-Tetraazidobenzoquinone
I couldnt find any reference to the reaction of hydroxylamine with triquinoyl so I looked at hydrazi ... |
23-5-2008 at 13:01
by: Axt |
N-Nitroimides
A rather insane explosive moiety N-N-NO2. I was looking at the synthesis of what looks to be the mos ... |
20-5-2008 at 16:19
by: Axt |
2,3,5,6-Tetraazidobenzoquinone
Since the topics turned into any energetic chloranil derivative, heres an idea to produce the hexaox ... |
19-5-2008 at 15:06
by: Axt |
Methyl Acetylides
Very interesting Schockwave, with both mercury and copper methylacetylides being non-explosive. Quit ... |
14-5-2008 at 11:16
by: Axt |
Halogenated Amines - the others
I've seen reference to NI3.NH3 being used to convert acetylene to tetraiodoethylene as well.
This ... |
14-5-2008 at 04:57
by: Axt |
Methyl Acetylides
The attachment contains the preparation of the mercury "salt" of methylacetylene. Its not a salt rat ... |
14-5-2008 at 03:34
by: Axt |
Methyl Acetylides
Even though the Ag salt is quite a weak explosive, resembles blackpowder in its effect. I'd be inter ... |
14-5-2008 at 03:26
by: Axt |
Halogenated Amines - the others
I mentioned previously in this thread that iodine under ethylenediamine turned red. Heres an article ... |
12-5-2008 at 13:27
by: Axt |
2,5-Dimethylfuran (Gasoline Replacement)
Attaching the 100 most relevant abstracts regarding the preparation of dimethylfuran, from scifinder ... |
9-5-2008 at 23:56
by: Axt |
CCl4/Al
Attaching abstracts on CCl4 + Al explosives. Also check US4233094. I've previously mentioned using C ... |
4-5-2008 at 07:08
by: Axt |
Nitration of xylene
Well take the hint Mason and dont come back.
Heres an article that supposedly gives the preparati ... |
4-5-2008 at 06:56
by: Axt |
Formic acid from Hexamine/HCl?
Would the reaction of hexamine with H2O2 + NaOH produce Na formate? this seems to work where formald ... |
2-5-2008 at 21:58
by: Axt |
Methyl Ethyl Ketone Peroxide
Do you really need a 5 page discussion on something that can very easily be tried, thus the word 'ex ... |
2-5-2008 at 06:25
by: Axt |
Tetrasulfur Tetranitride
Maybe the red colour is a result of an excess NH3, since the colour cant be reproduced by redisolvin ... |
2-5-2008 at 06:16
by: Axt |
Tetrasulfur Tetranitride
Thats wrong Picric-A, the precipitate is NH4Cl and S8, the N4S4 remains in solution, or is extracted ... |
2-5-2008 at 02:22
by: Axt |
Tetrasulfur Tetranitride
In all the years I've been around the forums I've never actually know anyone attempt it. Anyway I'm ... |
1-5-2008 at 10:16
by: Axt |
Halogenated Amines - the others
Okay, regarding halogenation of the oxyamines I've been going over stuff that I've already posted be ... |
30-4-2008 at 23:32
by: Axt |
Pentryl
Yes you an use dinitrobromobenzene for the condensation with ethanolamine. If you want reference to ... |
30-4-2008 at 17:45
by: Axt |
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