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Nitramides

Nitroxylic acid, HiNO . Yellow NajNOa formed by electrolysis NaN02 in NHj. Structure unknown free acid unknown. Nitramide, H2NNO2. A weak acid. [Pg.279]

Figure 7-3. Br nsted plot for the decomposition of nitramide catalyzed by substituted anilines. Figure 7-3. Br nsted plot for the decomposition of nitramide catalyzed by substituted anilines.
Thermal decomposition of nitramide, H2NNO2, or hyponitrous acid H2N2O2 (both of which have the empirical formula N2O.H2O) have also been used. The mechanisms of these and other reactions involving simple inorganic compounds of N have been reviewed. [Pg.444]

H2N2O2 Hyponitrous acid Weak acid HON=NOH, isomeric with nitramide, H2N-N02 salts are known (p. 460)... [Pg.459]

Following three phase transformations [951] (>298 K), NH C decomposition begins [915] in the solid phase at 423 K but only becomes extensive well above the melting point ( 440 K). Decomposition with the evolution of N20 and H20 from the melt is first order [952,953] (E = 153—163 kJ mole-1), the mechanism suggested involving intermediate nitramide formation. Other proposed schemes have identified NOj [954] or the radical NH2NO [955] (<473 K) as possible participants. Studies [956,957] have been made of the influence of additives on NH C decomposition. [Pg.201]

N,N Dinitro-N-methyl- ,2-diaminoethane 1 -methyl-3-nitro-1 -nitrosoguanidine Nitric amide (nitramide)... [Pg.172]

Lead methylenebis(nitramide) (/V,/V -Dinitromcthanediamine, lead (I I) salt) [86202-43-9] CH2N404Pb... [Pg.167]

Salts of the acidic dinitramine find use as oxidants in propellant formulations. The dinitramine itself is explosively unstable, though more stable than nitramide [1], Although described as relatively stable the sodium salt has an autoignition temperature of 123°C, the potassium 140°C [2],... [Pg.1603]

Nitramide is quite unstable and various reactions in which it is formed are violent. Attempts to prepare it by interaction of various nitrates and sulfamates showed that the reactions became explosive at specific temperatures. [Pg.1621]

A drop of cone, alkali solution added to solid nitramide causes a flame and explosive decomposition. [Pg.1621]

Nitramide decomposes explosively on contact with cone, sulfuric acid. [Pg.1621]

Both hyponitrous acid and nitroamide (also known as nitramide) have the formula H2N202. Draw the structures for these molecules and explain any difference in acid-base properties. [Pg.520]

Man gewinnt Ammoniumdinitramid durch Ammonolyse von Dinitroa-minen, welche durch stufenweise Nitrierung von Urethanen, p,p-lmino-dipropionitril Oder Nitramid entstehen. Die jeweils letzte Nitrierstufe erfordert starkste Nitrierreagenzien wie Nitroniumtetrafluoroborat Oder... [Pg.30]

Dithioglyoollic Acid Oxalyl Chloride Nitrourea Nitramide Ethyl Orthoformate Fumaric Acid Glutaric Acid Adipic Acid Pimelic Acid... [Pg.422]

Electron impact mass spectra of nitro compounds show generally [M — 0]+ ions, however, in low intensity. Several [M —0]+ ions, e.g. the [M— 16]+ of nitromethane44 and nitroethene45, has by tandem mass spectrometry unambiguously been demonstrated to be of the nitroso form. Particularly interesting is the use of the parent nitramide in NRMS study of the elusive nitrosamide46. [Pg.259]


See other pages where Nitramides is mentioned: [Pg.275]    [Pg.2092]    [Pg.240]    [Pg.27]    [Pg.340]    [Pg.346]    [Pg.459]    [Pg.68]    [Pg.211]    [Pg.825]    [Pg.413]    [Pg.165]    [Pg.240]    [Pg.222]    [Pg.362]    [Pg.1621]    [Pg.1647]    [Pg.40]    [Pg.111]    [Pg.213]    [Pg.213]    [Pg.213]    [Pg.264]    [Pg.397]    [Pg.883]    [Pg.124]   
See also in sourсe #XX -- [ Pg.8 , Pg.28 , Pg.29 ]




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ALIPHATIC NITRAMINES AND NITRAMIDES Nitramine (nitramide)

Base catalysis, decomposition nitramide

Decomposition of nitramide

Hydrolysis of nitramides and nitroureas

Methyl nitramide

NH2NO2 Nitramide

Nitramidates

Nitramide

Nitramide

Nitramide , decomposition reactions

Nitramide decomposition

Nitramide or Nitroxylamide

Nitramide, hydrolysis

Nitramides hydrolysis

Nitramides, decomposition

Nitramines, nitramides and nitrimines as explosives

Preparation of nitramines and nitramides

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