Jump to content
 







Main menu
   


Navigation  



Main page
Contents
Current events
Random article
About Wikipedia
Contact us
Donate
 




Contribute  



Help
Learn to edit
Community portal
Recent changes
Upload file
 








Search  

































Create account

Log in
 









Create account
 Log in
 




Pages for logged out editors learn more  



Contributions
Talk
 



















Contents

   



(Top)
 


1 Reactions  



1.1  Decomposition  





1.2  Sensitivity to friction  







2 Hazards  





3 References  














Tetrazene explosive






تۆرکجه
Čeština
Deutsch
فارسی
Français

Polski
Русский
Slovenčina
Српски / srpski
Srpskohrvatski / српскохрватски
Suomi

 

Edit links
 









Article
Talk
 

















Read
Edit
View history
 








Tools
   


Actions  



Read
Edit
View history
 




General  



What links here
Related changes
Upload file
Special pages
Permanent link
Page information
Cite this page
Get shortened URL
Download QR code
Wikidata item
 




Print/export  



Download as PDF
Printable version
 




In other projects  



Wikimedia Commons
 
















Appearance
   

 






From Wikipedia, the free encyclopedia
 


Tetrazene explosive
Structural formula
Ball-and-stick model
Names
IUPAC name

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

Other names

Tetracene[1]

Identifiers

CAS Number

  • (anhydrous): 776249-85-5 checkY
  • 3D model (JSmol)

    ECHA InfoCard 100.128.336 Edit this at Wikidata

    PubChem CID

    UNII

    CompTox Dashboard (EPA)

    • 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 checkY☒N ?)

    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.

    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.
  • ^ 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 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.
  • ^ 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&oldid=1218579406"

    Categories: 
    Nitrogen compounds
    Explosive chemicals
    Azo compounds
    Tetrazoles
    Hidden categories: 
    CS1: long volume value
    Chemical articles with multiple compound IDs
    Chemicals using indexlabels
    Chemical articles with multiple CAS registry numbers
    Articles without InChI source
    Chemical pages without ChemSpiderID
    Articles without EBI source
    Articles without KEGG source
    ECHA InfoCard ID from Wikidata
    Articles containing unverified chemical infoboxes
    Articles with short description
    Short description matches Wikidata
     



    This page was last edited on 12 April 2024, at 15:22 (UTC).

    Text is available under the Creative Commons Attribution-ShareAlike License 4.0; additional terms may apply. By using this site, you agree to the Terms of Use and Privacy Policy. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc., a non-profit organization.



    Privacy policy

    About Wikipedia

    Disclaimers

    Contact Wikipedia

    Code of Conduct

    Developers

    Statistics

    Cookie statement

    Mobile view



    Wikimedia Foundation
    Powered by MediaWiki