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Tetrazene explosive

chemical compound

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Record originEnglish Wikipedia
Text licenseCC BY-SA 4.0
Source revisionJun 18, 2026
Entity authorityQ425456 ↗
Source-derived summary

Tetrazene (1-(5-tetrazolyl)-3-guanyl tetrazene hydrate) is an explosive material used for sensitization of priming compositions. It is a derivative of the compound with the IUPAC name tetrazene.

Tetrazene is slightly more impact-sensitive than mercury fulminate. When pressed enough, its sensitivity is reduced or destroyed; this is known as dead pressing. It also decomposes in boiling water. In contact with fire, it readily explodes, producing large amounts of black smoke. It is prepared by reacting sodium nitrite with an aminoguanidine salt dissolved in acetic acid at 30–40 °C.

Commercially, tetrazene is added in a small proportions to increase the sensitivity of lead styphnate in cap compositions used both in centre-fire (eg shotgun cartridges) and rim-fire (eg 0.22" ammunition) applications. Cap compositions also contain a high proportion of barium nitrate as an oxidising agent, and scintillating compounds such as antimony disulphide or ground glass which cause the heat of the explosion when struck by the firearm firing pin to rapidly dissipate the main charge of either nitrocellulose or cordite.

Reactions

Decomposition

The decomposition of tetrazene is quite rapid around 90 °C. A sample of tetrazene was heated in an oven at 90 °C and its rate of thermal decomposition was monitored by infrared and ultraviolet spectroscopy. The thermal decomposition reaction is autocatalytic and it is likely that the same reaction can occur at even lower temperatures, however at much slower rates.

Editorial summary

“Tetrazene explosive” enters the record as chemical compound. Crown Archives preserves that source wording while asking what Tetrazene, explosive and chemical can confirm, complicate or overturn.

Editorial reviewUseful for establishing the present vocabulary of the subject while preserving a route back to the evidence on which that vocabulary rests. The current 228-word lead offers orientation but no explicit four-digit date, so chronology should not be assumed. The selected authority fields contribute no independent date. Its strongest next move is a source search built around Tetrazene, explosive and chemical.
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“Tetrazene explosive” is worth following because a concise public description often conceals a longer documentary argument. Here, Tetrazene, explosive and chemical provides the most credible route into that argument.

Evidence profile

The date and method of observation matter as much as the stated conclusion, especially where classification or consensus has changed. The source revision retrieved here is dated Jun 18, 2026. The linked authority identifier is Q425456. None of the 0 selected statements returned an explicit reference.

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Source & attribution

This entry incorporates text from “Tetrazene explosive” on English Wikipedia. Contributors are listed in the page history. Text is available under the Creative Commons Attribution-ShareAlike 4.0 License. Selected authority identifiers and statements are retrieved from Wikidata under CC0; their references and qualifiers remain part of the verification path.