55510-04-8 Usage
Uses
Used in Military Applications:
Tetrahydro-1,4-dinitroimidazo[4,5-d]imidazole-2,5(1H,3H)-dione is used as an explosive material in the military industry for its ability to create a powerful blast upon detonation. Its instantaneous explosion characteristic makes it suitable for various military applications, such as the creation of explosives for demolitions, mines, and other explosive devices.
Used in Research and Development:
In the field of scientific research, tetrahydro-1,4-dinitroimidazo[4,5-d]imidazole-2,5(1H,3H)-dione is utilized as a compound for studying the properties and behavior of explosives. Researchers can use tetrahydro-1,4-dinitroimidazo[4,5-d]imidazole-2,5(1H,3H)-dione to develop new methods for handling and controlling explosive materials, as well as to improve the safety measures and protocols associated with their use.
Used in Industrial Applications:
Tetrahydro-1,4-dinitroimidazo[4,5-d]imidazole-2,5(1H,3H)-dione is also employed in the industrial sector for various applications that require controlled explosive power. This can include activities such as mining, construction, and the demolition of structures. tetrahydro-1,4-dinitroimidazo[4,5-d]imidazole-2,5(1H,3H)-dione's ability to create a powerful blast makes it a valuable resource for these industries, provided that proper safety precautions are taken to minimize the risk of accidents and injuries.
Reactivity Profile
Materials in this group range from slight to strong oxidizing agents. If mixed with reducing agents, including hydrides, sulfides and nitrides, they may begin a vigorous reaction that culminates in a detonation. Nitroalkanes are milder oxidizing agents, but still react violently with reducing agents at higher temperature and pressures. Nitroalkanes react with inorganic bases to form explosive salts. The presence of metal oxides increases the thermal sensitivity of nitroalkanes. Nitroalkanes with more than one nitro group are generally explosive. The higher nitroalkanes are insoluble in water.
Health Hazard
Fire may produce irritating, corrosive and/or toxic gases.
Fire Hazard
MAY EXPLODE AND THROW FRAGMENTS 1600 meters (1 MILE) OR MORE IF FIRE REACHES CARGO.
Check Digit Verification of cas no
The CAS Registry Mumber 55510-04-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,5,1 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55510-04:
(7*5)+(6*5)+(5*5)+(4*1)+(3*0)+(2*0)+(1*4)=98
98 % 10 = 8
So 55510-04-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H4N6O6/c11-3-5-1-2(8(3)10(15)16)6-4(12)7(1)9(13)14/h1-2H,(H,5,11)(H,6,12)
55510-04-8Relevant academic research and scientific papers
Zharkov, Mikhail N.,Kuchurov, Ilya V.,Fomenkov, Igor V.,Zlotin, Sergei G.,Tartakovsky, Vladimir A.
, p. 15 - 16 (2015)
Dinitroglycolurils and 1,4,6-trinitrohexahydroimidazo[4,5-d]imidazol-2(1H)-one were prepared in 56-89% yield by N-nitration of the corresponding glycoluril precursors with dinitrogen pentoxide in liquid carbon dioxide.
Methodes de preparation de derives nitres et nitroacetyles du glycolurile (I)
Boileau, J.,Wimmer, E.,Carail, M.,Gallo, R.
, p. 465 - 469 (2007/10/02)
A procedure for preparing nitro and nitroacetyl derivatives of glycoluril is described, starting from tetraacetylglycoluril (TAGU).The method proceeds by nitrodeacetylation and (or) hydrolysis.New compounds have been prepared : mononitrodiacetylglycoluril (MONDAGU), dinitrodiacetylglycoluril (DINDAGU) and mononitroglycoluril (MONGU).A general synthetic scheme is proposed and discussed.Some properties of the new derivatives are presented.
