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Mr.Greeenix
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does someone know where the solubility differnences of Dingu and TNGU are.
TNGU soluable in Nitromethan I know...
I need them to see if there is some DINGU in my TNGU (made by Engangers method)
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Thraxx
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DINGU,Dinitroacetylenediurein
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-very small white or colorless crystals (my own experience is,that DINGU prepared with only nitric acid is brown and with nitric-sulfuric is white.The
brown crystals are smaller.)
-two isomers(1,3)small amount and unwanted, decomposed with boiling watter, (1,5) decomposed of amonia at RT
-stable in acid medium
-readily decomposed at alkaline hydrolysis
-decomposition beginns at 130C
-deflagration point at 225-250C
-sensitivity –much less sensitive than HMX,reffered like insensitive HE (IHE)
-solubility in conc. Nitric acid,in DMSO
-insoluble in water,nitrometan and in ordinary org solvents
-density-1,94
-rate of detonation-at 1,75 it is 7580 m/s
TENGU-soluble in nitrometan,
in dioxan /17g/100ml at 27C/
in glacial acetic acid /15g/100ml at 25 C/
History:
1888-Franchimont and Klobbie-synt.:1part of Glycoluril + 5 parts abs.nitric acid
1889-Ibid
1944-Blatt-synt.: nitrating Glycoluril +98%HNO3+aceticanhydrid at below 5C
1973-Boileau,Emeury,Kehren-Fr.patent : 7327038
[Edited on 15-10-2016 by Thraxx]
[Edited on 15-10-2016 by Thraxx]
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nlvince
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This seems to be pretty high yielding:
To a 500 mL round-bottom flask equipped with a stirbar was added 100 mL of H2O, glyoxal (20 g, 0.345 mol, 1.00 eq, 50 ml of a 40 wt. percent solution
in H2O), and urea (51.7 g, 0.862 mol, 2.50 eq). The reaction mixture was heated to 90 oC and was stirred for 5 min. Concentrated H2SO4 (4 mL) was
added dropwise over 5 min, and a white solid formed 10 minutes after addition of the acid. The reaction mixture was stirred for an additional 12 h.
The reaction mixture was cooled to room temperature, and a 50percent aqueous solution of NaOH was added until the pH of the reaction was adjusted to
14. The stirring was stopped, and the reaction mixture was cooled to 0 oC. The suspension was isolated by vacuum filtration on a Büchner funnel, and
the solid was washed with cold water (2 x 500 mL). The solid was left to dry on the Büchner funnel under suction for 3 h, was transferred to a 700 mL
beaker, and was dried for 16 h at 80 oC to yield 45.0 g (0.304 mol, 92percent yield) of glycoluril (1) as an off-white powder. m.p. =335.19 oC
I also have the reference but am not sure where to upload it
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Thraxx
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in the 50 ml of Glyoxal dissolve 86g of urea and put there quickly solution of 22 ml water + 37ml conc.H2SO4.It will heat and turn white and you will
shake it all the time of heating and if you want,then can you put the flask into the 65 C watterbath for 1 h.and then filtering washing drying.
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nlvince
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This patent describes the synthesis of sorguyl using 100% nitric acid and acetic anhydride. They claim 85% yield.
https://worldwide.espacenet.com/publicationDetails/originalD...
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PHILOU Zrealone
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Most amine base for common caged nitramine are high yielding...
-hexamine from aqueous CH2O and aqueous NH3
-glycoluril from urea and glyoxal
-...
PH Z (PHILOU Zrealone)
"Physic is all what never works; Chemistry is all what stinks and explodes!"-"Life that deadly disease, sexually transmitted."(W.Allen)
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Mr.Greeenix
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Does somebody know anything about the compound 1,1,2,2-tetranitroaminoetanu, which is supposedly the hydrolisation product of TNGU.
Detonation velocity is 9500m/s
Detonation pressure 41GP
The only thing I can find on this compound is a polish paper which i unfortunatly can not read. 
Maybe someone who speaks polish is so keen and translates the synthesis and/or other important information.
I am really interested but there is nothing. If someone knows something please feel free to post it. 
Attachment: 1,1,2,2-tetranitroaminoetanu.pdf (652kB)
This file has been downloaded 587 times
Thank you!
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PHILOU Zrealone
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Quote: Originally posted by Mr.Greeenix  | Does somebody know anything about the compound 1,1,2,2-tetranitroaminoetanu, which is supposedly the hydrolisation product of TNGU.
Detonation velocity is 9500m/s
Detonation pressure 41GP
The only thing I can find on this compound is a polish paper which i unfortunatly can not read.
Maybe someone who speaks polish is so keen and translates the synthesis and/or other important information.
I am really interested but there is nothing. If someone knows something please feel free to post it.
Thank you!
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Such geminal nitramines (*) are powerful but quite sensitive (shock, heat, friction) vs parent nitramines and they also lacks stability for
storage...they are very acidic and reacts with metals to make sensitive metal nitramines...the H onto the NH is even more acidic than into carbon
nitramines holding max one nitramine per carbon atom (viccinal nitramines)(**).
They will be very happy to split off a nitramide molecule (H2N-NO2 (unstable)) and to provide a nitroimide group.
R-CH(-NH-NO2)2 <--==> R-CH=N-NO2 + H2N-NO2
H2N-NO2 ---> H2O + N2O + N2 + O2
(*)
Methylene dinitramine CH2(-NH-NO2)2
Ethylene bis-dinitramine (N,N,N',N'-tetranitro-ethylene-1,2-diamine) (O2N-NH-)2CH-CH(-NH-NO2)2
(**)
Methyl nitramine CH3-NH-NO2
Ethylene dinitramine O2N-NH-CH2-CH2-NH-NO2
Propane trinitramine O2N-NH-CH2-CH(-NH-NO2)-CH2-NH-NO2
PH Z (PHILOU Zrealone)
"Physic is all what never works; Chemistry is all what stinks and explodes!"-"Life that deadly disease, sexually transmitted."(W.Allen)
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Microtek
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When I wrote my dissertation, I investigated the possibilty of condensing tetranitraminoethane with disulfaminotetrahydroxypiperazine and then
nitrolysing the sulfonic groups to form HNIW without annoying catalytic hydrodebenzylation.
Unfortunately, the results were inconclusive.
About the paper: Why don't you copy/paste it into google translate? It won't be a perfect translation, but usually enough to catch the essentials
(especially if you know something about the subject).
[Edited on 10-12-2016 by Microtek]
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