Abstract: A method for preparing an insensitive bis(2,2-dinitropropyl)nitramine (BDNPN) as a fine powder which exhibits desirable insensitive munitions (IM) characteristics for use alone or compounded with other energetic materials such as RDX.

Abstract: A lead-free primer energetic composition including Cyanuric Triazide (60%), Tetracene (5%), Barium Nitrate (20%) and Antimony Trisulfide (15%) is produced. The lead-free primer energetic composition is used to construct a primary detonator including a transfer charge of Cyanuric Triazide, which produces a further initiation train that may subsequently detonate a secondary explosive, i.e., HDX, RDX, or a pyrotechnic device.

Abstract: 1-Methyl-2,4,5-Trinitroimidazole is synthesized starting from 4-nitroimidazole using stepwise nitration method and further methylation using Dimethylsulphate. It is relatively insensitive to impact and its thermal stability is excellent. The calculated detonation properties indicate that its performance is about 30% better than TATB. It can be prepared easily, with reasonable yield, starting from commercially available Imidazole. Results from impact sensitivity, friction sensitivity, time-to-explosion temperature and vacuum stability tests indicate that it is less sensitive than both RDX and HMX. The good oxygen balance and measured heat of formation data of this material indicate that its propellant performance should be good.

Abstract: The invention relates to a novel polyazido compound: 2,2-dinitro-1,3-diazidopropane.

Abstract: The compound 3a,8a-bis-azidomethyl-3a,4,8a,9-tetrahydro-3H,8H-bis-[1,2,3]triazolo[1,5-a;1?,5?-d]pyrazine, whose structure is depicted below, is disclosed:

Abstract: The compound 2,2-bis(azidomethyl)oxirane, whose structure is depicted below, is disclosed:

Abstract: This invention relates to a series of novel compounds having the general structures A and B: including 2-azido-2-azidomethyl-1,3-diazidopropane (1), 2-azidomethyl-2-hydroxy-1,3-diazidopropane (2), 2-azidomethyl-2-nitrato-1,3-diazidopropane (3), 2-azidomethyl-2-nitro-1,3-diazidopropane (4), 2,2-dinitro-1,3-diazidopropane (5), methallyidiazide (6), a dimer of methallyidiazide (6), comprising 3a,8a-Bis-azidomethyl-3a,4,8a,9-tetrahydro-3H,8H-bis[1,2,3]triazolo[1,5-a;1?,5?-d]pyrazine (6-Dimer), 1,3-diazidoacetone (7), and 2-Oximido-1,3-diazidopropane (8). Also shown are reaction intermediates of these compounds, including 2,2-bis(chloromethyl)oxirane (9), and 2,2-bis(azidomethyl)oxirane (10).

Abstract: New aza azetidinium sulfate compounds are described which can be intermediates in the preparation of azabicyclobutane.

Abstract: A novel cyclotetraphosphazene compound, 1,1-diamino-3,3,5,5,7,7-hexaazidocyclotetraphosphazene, is disclosed which has application as an energetic compound and percussion primer. Also disclosed is a method of preparing the compound.

Abstract: A novel cyclotetraphosphazene compound, 1,5-diamino-1,3,3,5,7,7-hexaazidocyclotetraphosphazene, is disclosed which has application as an energetic compound. Also disclosed is a method of preparing the compound.

Abstract: Processes and compositions for nitration of N-substituted isowurtzitane compounds with concentrated nitric acid at elevated temperatures to form HNIW and recovery thereof with high yields and purities. Polymorphic conversions to the epsilon HNIW crystal form at quanititative yields are also described.

Abstract: Processes and compositions for nitration of N-substituted isowurtzitane compounds with concentrated nitric acid at elevated temperatures to form HNIW and recovery of gamma HNIW with high yields and purities. Polymorphic conversion of HNIW crystals to epsilon HNIW crystals is also disclosed.

Abstract: Overall, the invention provides the chemistry for the compounds and for the processes to prepare compounds derived from 1,5-diazacyclooctanes. This makes available high density, high melting point, thermally stable small and medium ring nitrogen heterocycles that may also contain N-nitro, C-nitro or other functional groups. The compounds include cyclooctanes, bicyclo octanes, propellanes and functionalized derivatives of the above compounds. The preparations can include transannular cyclizations. The materials have several applications; e.g., the polynitro compounds are energetic materials.

Abstract: Azabicylobutane can be produced by reacting azetidines under aqueous conditions to eliminate aza and 3-position substituents to effect cyclization. New azetidinyl compounds are described which can be intermediates in the preparation of the azabicyclobutane.

Abstract: TNAZ can be prepared directly from N-tertiarybutyl-3,3-dinitroazetidine compounds. The compounds may be in the form of the tertiary amine or the quaternary amine. The reaction is in the presence of acetic anhydride and nitrate ions. It gives high yields and uses mild conditions.

Abstract: ADNAZ, N-acetyl, 3,3 dinitroazetidine, is a new compound and this invention provides the compound, its compositions, preparation and uses. As a compound, it forms a eutectic with TNAZ. It can be used to prepare other compounds. It can be readily nitrated to remove the acetyl group and form TNAZ.

Abstract: New N-nitro, 3 substituted azetidine compounds are disclosed and these are sed in processes to prepare TNAZ.

Abstract: Method of synthesizing a 1,3,3 trinitroazetidine compound (TNAZ) comprising the steps of:selecting a compound of the formula I: ##STR1## wherein R' is one of hydrogen and an organic group and R is selected from the group consisting of electron withdrawing and electron donating groups; and,reacting the selected compound with a nitrolyzing agent such that a TNAZ compound is formed from the reaction.

Abstract: Energetic nitramine containing cyclotriphosphazene which include 1,1,3,3,-tris-spiro(N,N'-dinitroethylenediamino)cyclotriphosphazene, 1,1-spiro(ethylenediamino)-3,3,5,5-bis-spiro(N,N'-dinitroethylenediamino)c yclotriphosphazene, 1,1,3,3-bis-spiro(N,N'-dinitroethylenediamino)-5,5-dichlorocyclotriphospha zene, 1,1,3,3-bis-spiro(N,N'-dinitroethylenediamino)-5,5-difluorocyclotriphospha zene, 1,1-spiro(N,N'-dinitroethylenediamino)-3,3,5,5-bis-spiro(ethylenediamino)c yclotriphosphazene, 1,1-spiro(ethylenediamino)-3,3-spiro(N,N'-dinitroethylenediamino)-5,5-dich lorocyclotriphosphazene, 1,1-spiro(ethylenediamino)-3,3-spiro(N,N'-dinitroethylenediamino)-5,5-difl uorocyclotriphosphazene, 1,1-spiro(N,N'-dinitroethylenediamino)-3,3,5,5-tetrachlorocyclotriphosphaz ene, and 1,1-spiro(N,N'-dinitroethylenediamino)-3,3,5,5-tetrafluorocyclotriphosphaz ene, which can be used in explosive compositions.

Abstract: 4,4-Dinitroadamantane-2,6-dione,6, and a method of making the same.