Tetrazene explosive

Tetrazene explosive
Names
IUPAC name
1-(5-tetrazolyl)-3-guanyl tetrazene hydrate
Other names
Tetracene
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.128.336
UNII
  • InChI=1S/C2H6N10.H2O/c3-1(4)12(5)11-8-2-6-9-10-7-2;/h11H,5H2,(H3,3,4);1H2
    Key: XLZZIAVGIPSWEG-UHFFFAOYSA-N
  • InChI=2S/C2H6N10/c3-1(4)12(5)11-8-2-6-9-10-7-2/h5H2,(H3,3,4)(H,6,7,9,10)
  • (anhydrous): Key: WSLWDHGXSGRREP-UHFFFAOYSA-N
  • (anhydrous): N=C(N)N(N)/N=N/C1=NNN=N1
Properties
C2H6N10·H2O
Molar mass 188.15 g/mol
Appearance Pale yellow/colorless crystal plates
Density 1.7 g/cm3
Boiling point Decomposes at 160 °C (320 °F; 433 K)
Explosive data
Shock sensitivity High
Friction sensitivity High
Detonation velocity ~4000 m/s
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

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.