Tetrazene explosive

Names
IUPAC name

1-(5-tetrazolyl)-3-guanyl tetrazene hydrate

Other names

Tetracene[1]

Identifiers

CAS Number

* 31330-63-9 Y
* (anhydrous): 776249-85-5 Y

3D model (JSmol)

* (anhydrous): Interactive image

ChemSpider |

* 4589066
* (anhydrous): 58541346

PubChem CID

* 5486788
* (anhydrous): 123436

UNII |

* U3EB9RU4TD Y

InChI

* 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

SMILES

* (anhydrous): N=C(N)N(N)/N=N/C1=NNN=N1

Properties

Chemical formula

| C2H6N10·H2O
Molar mass | 188.15 g/mol
Appearance  | Pale yellow/colorless crystal plates[1]
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)[2] 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.

## Contents

* 1 Reactions
* 1.1 Decomposition
* 1.2 Sensitivity to friction
* 2 Hazards
* 3 References

## 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.[3] 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.

### Sensitivity to friction

Many explosives are considered to be highly sensitive to mechanical stimuli such as impact, friction, stab, heat, static electricity, flame, etc. Since explosive compounds are subject to friction practically every time they are handled, it is of particular interest to be aware of the sensitivity to friction. The sensitivity of tetrazene was determined using a FSKM-PEx friction sensitivity tester.[4] The probability of ignition of tetrazene is 100 percent likely at 27N of frictional force.[4]

## Hazards

Instances of occupational rhinitis, dermatitis, and asthma have been reported due to prolonged exposure to tetrazene.[5]

## References

1. ↑ 1.0 1.1 "MIL-T-46938C, MILITARY SPECIFICATION: TETRACENE" (PDF). United States Department of Defense. 16 May 1994. http://www.everyspec.com/MIL-SPECS/MIL-SPECS-MIL-T/MIL-T-46938C_14978/.
2. ↑ Duke, J. R. C. (1971). "X-Ray crystal and molecular structure of 'tetrazene', ('Tetracene'), C2H8N10O". Journal of the Chemical Society D: Chemical Communications 1971 (1): 2–3. doi:10.1039/C29710000002.
3. ↑ "Thermal Decomposition of Tetrazene at 90°C". Melbourne, Victoria: Department of Defence. 1978. http://apps.dtic.mil/dtic/tr/fulltext/u2/a056265.pdf.
4. ↑ 4.0 4.1 Matyáš, R.; Šelešovský, J.; Musil, T. (2012). "Sensitivity to friction for Primary Explosives". Journal of Hazardous Materials 213–214: 236–41. doi:10.1016/j.jhazmat.2012.01.085. PMID 22349715. Bibcode: 2012JHzM..213..236M.
5. ↑ Burge, P. S.; Hendy, M.; Hodgson, E. S. (1984). "Occupational asthma, rhinitis, and dermatitis due to tetrazene in a detonator manufacturer". Thorax 39 (6): 470–1. doi:10.1136/thx.39.6.470. PMID 6235620.

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*[CID]: Compound ID