Pentaerythritol trinitrate

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Structural formula
Structural formula of pentaerythritol trinitrate
General
Surname Pentaerythritol trinitrate
other names
  • Pentrinitrol
  • Petrin
  • Pentaerythritol trinitrate
  • Nitric acid pentaerythritol triester
Molecular formula C 5 H 9 N 3 O 10
External identifiers / databases
CAS number 1607-17-6
EC number 216-529-7
ECHA InfoCard 100.015.027
PubChem 15353
Wikidata Q2069313
properties
Molar mass 271.14 g mol −1
Melting point

<25 ° C

solubility

slightly soluble in water: 7050 mg l −1 (20 ° C)

safety instructions
GHS hazard labeling
no classification available
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Pentaerythritol trinitrate (Petrin) is a little-known yet powerful explosive with a detonation speed of up to 8450 m · s −1 . Like the more common pentaerythritol granitrate known as nitropenta , trinitrate also has a strong vasodilatory effect .

Manufacture and composition

Pentaerythritol trinitrate is a nitrate (an ester of nitric acid) of pentaerythritol. It occurs either as a by-product in the classic esterification of pentaerythritol with nitric acid or is obtained by nitration of pentaerythritol with a mixed acid. A small part of the tetranitrate is produced there.

properties

The detonation speed is at a maximum density of 1.54 g / cm³ up to 8450 m · s −1 . In addition, pentaerythritol trinitrate has a molar mass of 271.14 g / mol and an oxygen balance of −26.6%.

The biggest disadvantage is the shorter storage time of 5 to 10 years compared to Nitropenta.

Legal position

The handling, traffic, transport and import of Petrin are subject to the Explosives Act .

Individual evidence

  1. a b Entry on pentaerythritol trinitrate in the ChemIDplus database of the United States National Library of Medicine (NLM), accessed on November 27, 2018.
  2. This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
  3. ^ Josef Köhler, Rudolf Meyer, Axel Homburg: Explosivstoffe. 10th edition, Wiley-VCH, Weinheim 2008, ISBN 978-3-527-32009-7 , p. 231.