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R. Meyer J. Köhler A. Homburg Explosives

R. Meyer J. Köhler A. Homburg Explosives

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Tetracene<br />

Tetracene<br />

tetrazolyl guanyltetrazene hydrate; Tetrazen; tétrazéne*)<br />

feathery, colorless to pale yellow crystals<br />

empirical formula: C2H8N10O<br />

molecular weight: 188.2<br />

energy of formation: +270.2 kcal/kg = +1130 kJ/kg<br />

enthalpy of formation: +240.2 kcal/kg = +1005 kJ/kg<br />

oxygen balance: –59.5%<br />

nitrogen content: 74.43%<br />

density: 1.7 g/cm3 lead block test: 155 cm3 /10 g<br />

deflagration point: ca. 140 °C = 294 °F<br />

impact sensitivity: 0.1 kp m = 1 N m<br />

Tetrazene is classified as an initiating explosive, but its own initiation<br />

effect is weak.<br />

It is practically insoluble in water, alcohol, ether, benzene, and carbon<br />

tetrachloride. It is prepared by the reaction between aminoguanidine<br />

salts and sodium nitrite.<br />

Tetrazene is an effective primer which decomposes without leaving<br />

any residue behind. It is introduced as an additive to erosion-free<br />

primers based on lead trinitroresorcinate in order to enhance the<br />

response. Its sensitivity to impact and to friction are about equal to<br />

those of mercury fulminate.<br />

Specifications<br />

moisture: not more than 0.3 %<br />

reaction, water extract to<br />

universal indicator paper: no acid<br />

indication<br />

mechanical impurities: none<br />

pouring density; about 0.3 g/cm 3<br />

deflagration point:<br />

not below 138 °C = 280 °F<br />

310<br />

* The structural formula found in the earlier literature: HN-C(=NH)-NH-NH-N=N-<br />

C(=NH)-NH-NH-NO was corrected in 1954 by Patinkin (Chem. Zentr. 1955,<br />

p. 8377).

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