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Oxanilide

On nitration, oxanilide yields expl tetra- and hexanitrates (see below)... [Pg.438]

Origin. A.G. Perkins in 1892 obtained TNO directly by heating a soln of finely powdered oxanilide in nitric acid. He also obtained the same compd by the action of a cooled mixt of nitric and sulfuric acids on oxanilide and pptg the product by pouring the soln into w (Ref 2) Impact Sensitivity. PicArsnapp, llmg sample 30 inches... [Pg.439]

J. Kristal, Substitution of Tetranitro Oxanilide and Hexanitro Oxanilide for Tetranitrocarba-zole , PIcArsn Pyrotechnic Research Laboratory Rept 54-TF1-88 (20 Dec 1954) 4) S. Living-... [Pg.439]

Preparation. To prepare Hexanitro-oxanilide, first prepare Tetranitro-oxanilide as described above under the entry 2,4,2 , 4 Tetranitro-oxanilide (TNO) ... [Pg.440]

Man erhalt die Verbindung durch Nitrierung von Oxanilid. Der Stoff ist interessant als relativ hoch-temperatur-stabiler Sprengstoff. [Pg.180]

N 21.96% crysts, mp 295-300°(dec) si sol in hot ale Sc benz very low expin temp. It was prepd by nitrating oxanilide. Its power Sc brisance are comparable with those values of TNT Pb block expansion test — 70% Picric Acid. It is reported to be chemically unstable or reactive with moisture (Refs 6, 7, 8 8t 9) Refs 1) Beil 12, 284, (207) Sc [l65]... [Pg.364]

TB tracer bullet T eNOx or TNO tetr an itro oxanilide... [Pg.774]

Figure 6.15 Chemical structures of some polymer photostabilizers (a) 2-hydroxybenzophenone, (b) hydroxybenzotriazole, (c) oxanilide... Figure 6.15 Chemical structures of some polymer photostabilizers (a) 2-hydroxybenzophenone, (b) hydroxybenzotriazole, (c) oxanilide...
Carboxy deriv, lfts + HzO (from w), at ca 210° converts to oxanilide -3,3-dicarboxylic acid (Ref 2). Other props methods of prepn are given in the refs... [Pg.461]

This substance, m.p. 295-300°, results from the direct nitration of oxanilide.119 It is stable and about as powerful as TNT, and is reported to explode with the production of a temperature which is distinctly lower than that produced by many high explosives. [Pg.188]

Oxanilide and many other carbonaceous materials, incorporated in the grains of colloided powder, yield powders which are flashless in guns of the smaller calibers and, in many cases, are as powerful, weight for weight, as powders which contain none of the inert, or at least non-explosive, ingredients. If nitrocellulose burning in the gun produces 1 mol of carbon dioxide and a certain amount of other gaseous products, then nitrocellulose plus 1 mol of carbon under the same conditions will produce 2 mols of... [Pg.326]

The compound is prepared by the direct nitration of oxanilide (Mixter and Walther [40]). Domanski and Mieszkis [41] investigated the explosive properties of hexanitro-oxanilide and found the following values for the rate of detonation of the pressed product mixed with 2% of dinitrotoluene ... [Pg.570]

This compound is prepared by nitration of oxanilide. It is of interest as being relatively stable at high temperatures. The decomposition reaction above 304 °C is endothermic. [Pg.233]

See other pages where Oxanilide is mentioned: [Pg.436]    [Pg.438]    [Pg.438]    [Pg.439]    [Pg.439]    [Pg.439]    [Pg.440]    [Pg.440]    [Pg.228]    [Pg.76]    [Pg.83]    [Pg.587]    [Pg.162]    [Pg.479]    [Pg.356]    [Pg.405]    [Pg.761]    [Pg.802]    [Pg.145]    [Pg.200]    [Pg.18]    [Pg.188]    [Pg.326]    [Pg.593]    [Pg.762]    [Pg.1364]    [Pg.66]    [Pg.66]    [Pg.66]    [Pg.570]    [Pg.1364]   
See also in sourсe #XX -- [ Pg.188 , Pg.326 ]

See also in sourсe #XX -- [ Pg.188 , Pg.326 ]

See also in sourсe #XX -- [ Pg.557 ]

See also in sourсe #XX -- [ Pg.409 ]

See also in sourсe #XX -- [ Pg.236 ]



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Aromatic oxanilides

Hexanitro-oxanilid

Hexanitro-oxanilide

Nitration oxanilide

Oxanilides

Oxanilides

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