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Hexanitrodiphenyl sulfide

HFI height finding instrument HNDPhSfi hexanitrodiphenyl sulfide... [Pg.747]

CA 8,2253(1914XAn expl, for primer detonator caps or for filling projectiles, torpedoes or mines, is prepd from Hexanitrodiphenyl sulfide in HN03 by treating it with oxidg agents, to yield Hexanitrosulfobenzide) 19)C.F.von Girsewald,... [Pg.190]

The action of nitric acid on hexanitrodiphenyl sulfide yields a substance, faintly yellowish crystals, m.p. 307°, which Stett-bacher believes to be the sulfone, not the peroxide as the patent118 states, for the reason that it is stable at elevated temperatures... [Pg.187]

Canadian Explosives, Ltd., patented use of hexanitrodiphenyl sulfide in making cap compositions for primers. [Pg.13]

Uses During World War I, the Germans used drop bombs containing mixtures of TNT or trinitroanisole and hexanitrodiphenyl sulfide. It is also suitable for detonating compositions. [Pg.84]

During the first World War the Germans used a mixture of trinitroanisol and hexanitrodiphenyl sulfide in bombs. [Pg.385]

Tlie action of nitric acid on hexanitrodiphenyl sulfide yields a... [Pg.390]

Several nitro compounds are soluble in chlorine trifluoride, but the solutions are extremely shock-sensitive. These include trinitrotoluene, hexanitrobiphenyl, hexanitrodiphenyl-amine, -sulfide or -ether. Highly chlorinated compounds behave similarly. [Pg.1344]

See other pages where Hexanitrodiphenyl sulfide is mentioned: [Pg.452]    [Pg.190]    [Pg.22]    [Pg.187]    [Pg.187]    [Pg.188]    [Pg.452]    [Pg.38]    [Pg.83]    [Pg.83]    [Pg.123]    [Pg.452]    [Pg.316]    [Pg.452]    [Pg.330]    [Pg.338]    [Pg.390]    [Pg.390]    [Pg.452]    [Pg.649]   
See also in sourсe #XX -- [ Pg.126 , Pg.127 , Pg.159 ]



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Hexanitrodiphenyl

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