PETN

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PETN
Identifiers
CAS number [78-11-5]
PubChem 6518
SMILES
Properties
Molecular formula C5H8N4O12
Molar mass 316.137 g/mol
Density 1.77 g/cm3 at 20 °C
Melting point

141.3 °C, 414 K, 286 °F

Explosive data
Shock sensitivity Medium
Friction sensitivity Medium
Explosive velocity 8400 m/s
RE factor 1.66
Hazards
Autoignition
temperature
190 °C
Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox references

Pentaerythritol tetranitrate (PETN, also known as pentrite, or rarely and primarily in German as nitropenta) is one of the most powerful high explosives known, with a relative effectiveness factor (R.E. factor) of 1.66.

Contents

[edit] Uses

The most obvious use of PETN is as an explosive. It is more sensitive to shock or friction than TNT or tetryl, and it is never used alone as a booster. It is primarily used in booster and bursting charges of small caliber ammunition, in upper charges of detonators in some land mines and shells, and as the explosive core of detonation cord.[citation needed]

Apart from this, PETN is used as a vasodilator, similar to nitroglycerin. A medicine for heart disease, Lentonitrat, is nearly pure PETN.[1]

[edit] Production

PETN's preparation involves the nitration of pentaerythritol with a mixture of concentrated nitric and sulfuric acid. The preferred method of nitration is the ICI method, which utilizes concentrated nitric acid (98%+) alone, as mixed acid can create unstable sulfonated by-products.

C(CH2OH)4 + 4HNO3 → C(CH2ONO2)4 + 4H2O

[edit] History

Penthrite was first synthesized in 1891 by Tollens and Wiegand by nitration of pentaerythritol. In 1912, after being patented by the German government, the production of PETN started. PETN was used by the German army in World War I. [2] PETN is also one of the ingredients in Semtex plastic explosive. PETN was the explosive chosen by Richard Reid, which could have been used to blow up a 767 traveling from Paris to Miami if he wasn't stopped first.[citation needed]

[edit] See also

[edit] References

  1. ^ Russek H. I. (1966). "The therapeutic role of coronary vasodilators: glyceryl trinitrate, isosorbide dinitrate, and pentaerythritol tetranitrate.". American Journal of Medical Science 252 (1): 9–20. doi:10.1097/00000441-196607000-00002. PMID 4957459. 
  2. ^ Stettbacher, Alfred (1933). Die Schiess- und Sprengstoffe. Barth, 459. 

[edit] External links

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