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Nitration of Tris????
Thanks solo.
<i>"...the target nitroxyalkyl nitrates are separated from the reaction mixtur ... |
6-11-2006 at 07:53
by: Axt |
Nitration of Tris????
Reviving the topic, Attached is the synthesis of Tris(nitroxymethyl)methylamine via FNO2, OK thats n ... |
5-11-2006 at 02:16
by: Axt |
Sorguyl
[quote][i]Originally posted by chemoleo[/i]
Given that it is an acid, I imagine it'd be very diffic ... |
3-11-2006 at 11:21
by: Axt |
Sorguyl
Glycoluril is relatively insoluble so the condensation is very easy in acidic aqueous solution.
G ... |
1-11-2006 at 22:04
by: Axt |
Sorguyl
Thanks solo, nice info. Well it only referred to P2O5/HNO3 but didnt detail it. It referenced to PAT ... |
1-11-2006 at 08:31
by: Axt |
Hexanitroethane
[quote][i]Originally posted by Nitrojet[/i]
Do you have any details of synthesis following Diiodace ... |
28-10-2006 at 04:23
by: Axt |
Hexanitroethane
I wouldnt say it clearly shows anything, could be ANFO for all we know. Much better to show before ' ... |
27-10-2006 at 19:37
by: Axt |
FOX-7
OK, never clicked the second link. The article I attached just mentions to evaporate at <30°C wh ... |
25-10-2006 at 03:16
by: Axt |
Sorguyl
Propellants, Explosives, Pyrotechnics
Paste "Nitroureas II. Synthesis of Bicyclic Mono- and Dinit ... |
25-10-2006 at 01:53
by: Axt |
FOX-7
[quote][i]Originally posted by Nitrojet[/i]
Megalomania's method of synthesis of Fox-7 actually wor ... |
25-10-2006 at 01:45
by: Axt |
Exotic Primaries - Complex Salts
[quote][i]Originally posted by pdb[/i]
Any idea of what this stuff could be ? [/quote]
Isn't it ... |
24-10-2006 at 15:25
by: Axt |
Sorguyl
Can you get P2O5? N2O5 doesnt need to be isolated as such. HNO3/P2O5 will suffice and should be as r ... |
24-10-2006 at 15:09
by: Axt |
Hexanitroethane
Do you have the details of the synthesis via bromopicrin?
I've never seen any "numbers" specific ... |
23-10-2006 at 07:28
by: Axt |
Organic Hypochlorites
[quote][i]Originally posted by Zinc[/i]
Axt Did you try it? If yes what ratios did you use? [/quote ... |
22-10-2006 at 21:42
by: Axt |
Hexanitroethane
http://pdf.aiaa.org/jaPreview/AIAAJ/1963/PVJAPRE1544.pdf
Though its density seems to be debated.
... |
22-10-2006 at 12:53
by: Axt |
Pseudonitrosites
Attaching article on "methylnitrosolic acid". C-nitroso compounds being rare, and the fact thats it ... |
11-10-2006 at 15:49
by: Axt |
hydrazodicarbonamide
[quote][i]Originally posted by chemoleo[/i]
Do you have possibly solubility data on biurea? Maybe t ... |
28-9-2006 at 18:55
by: Axt |
hydrazodicarbonamide
Yes, Cl2 will add directly to urea, producing HCl. I imagine the ZnO is used to buffer the solution ... |
28-9-2006 at 07:43
by: Axt |
hydrazodicarbonamide
hydrazodicarbonamide (aka biurea) H2N-CO-NH-NH-CO-NH2
<b>Biurea from urea & hydrazine&l ... |
27-9-2006 at 22:49
by: Axt |
Methylenediisonitramine
The ammonium salt is mentioned in the article attached above. The sodium salt was "suprisingly solub ... |
22-9-2006 at 19:55
by: Axt |
Methylenediisonitramine
Carrying on with the analogies, sodium trioxodinitrate is structurally simular. Na-O-NO=NO-Na could ... |
22-9-2006 at 11:23
by: Axt |
Methylenediisonitramine
Was looking at "potassium dinitrososulfite" in Brauer (pg. 504). Looked up its structure [attached] ... |
22-9-2006 at 10:52
by: Axt |
Perchlorate compositions
Eh... this topic is very random.
[quote][i]Originally posted by quicksilver[/i]
CHLORATOTRIMERCU ... |
19-9-2006 at 18:35
by: Axt |
The Ultimate Energetic Compound
The triazone fertiliser mentioned in the PEP article as the most convenient precursor is patented US ... |
17-9-2006 at 21:54
by: Axt |
Glyoxime, Diaminofurazan and Some Energetic Derivatives
I tried to form a peroxidic product of Diaminofurazan by condensing it with formaldehyde & H2O2. ... |
15-9-2006 at 23:36
by: Axt |
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