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Tetrazene explosive

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 explosive
Names
IUPAC name
1-(5-tetrazolyl)-3-guanyl tetrazene hydrate
Other names
Tetracene[1]
Identifiers
  • 31330-63-9 Y
  • (anhydrous): 776249-85-5 Y
3D model (JSmol)
  • Interactive image
ECHA InfoCard 100.128.336
  • 5486788
UNII
  • U3EB9RU4TD Y
  • DTXSID10953376
  • 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[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 ?)

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.

Reactions Edit

Decomposition Edit

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 Edit

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 Edit

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

References Edit

  1. ^ a b "MIL-T-46938C, MILITARY SPECIFICATION: TETRACENE" (PDF). United States Department of Defense. 16 May 1994.
  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. ^ Bird, R.; Power, A. (1978). "Thermal Decomposition of Tetrazene at 90°C" (PDF). Melbourne, Victoria: Department of Defence. MRL-R-710 AR-000-886. (PDF) from the original on April 29, 2014.
  4. ^ a b 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.
  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. PMC 459834. PMID 6235620.

tetrazene, explosive, tetrazene, tetrazolyl, guanyl, tetrazene, hydrate, explosive, material, used, sensitization, priming, compositions, derivative, compound, with, iupac, name, tetrazene, namesiupac, name, tetrazolyl, guanyl, tetrazene, hydrateother, names, . 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 explosive NamesIUPAC name 1 5 tetrazolyl 3 guanyl tetrazene hydrateOther names Tetracene 1 IdentifiersCAS Number 31330 63 9 Y anhydrous 776249 85 5 Y3D model JSmol Interactive imageECHA InfoCard 100 128 336PubChem CID 5486788UNII U3EB9RU4TD YCompTox Dashboard EPA DTXSID10953376SMILES N C N N N N N C1 NNN N1PropertiesChemical formula C2H6N10 H2OMolar mass 188 15 g molAppearance Pale yellow colorless crystal plates 1 Density 1 7 g cm3Boiling point Decomposes at 160 C 320 F 433 K Explosive dataShock sensitivity HighFriction sensitivity HighDetonation velocity 4000 m sExcept where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa N verify what is Y N Infobox references 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 Contents 1 Reactions 1 1 Decomposition 1 2 Sensitivity to friction 2 Hazards 3 ReferencesReactions EditDecomposition Edit 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 Edit 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 EditInstances of occupational rhinitis dermatitis and asthma have been reported due to prolonged exposure to tetrazene 5 References Edit a b MIL T 46938C MILITARY SPECIFICATION TETRACENE PDF United States Department of Defense 16 May 1994 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 Bird R Power A 1978 Thermal Decomposition of Tetrazene at 90 C PDF Melbourne Victoria Department of Defence MRL R 710 AR 000 886 Archived PDF from the original on April 29 2014 a b Matyas R Selesovsky 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 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 PMC 459834 PMID 6235620 Retrieved from https en wikipedia org w index php title Tetrazene explosive amp oldid 1124583625, wikipedia, wiki, book, books, library,

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