Difference between revisions of "Pentaerythritol tetranitrate"
Line 158: | Line 158: | ||
*[http://www.sciencemadness.org/talk/viewthread.php?tid=22698 Question about PETN] | *[http://www.sciencemadness.org/talk/viewthread.php?tid=22698 Question about PETN] | ||
*[http://www.sciencemadness.org/talk/viewthread.php?tid=63225 PETN recrystallisation procedure for LOW density] | *[http://www.sciencemadness.org/talk/viewthread.php?tid=63225 PETN recrystallisation procedure for LOW density] | ||
+ | *[http://www.sciencemadness.org/talk/viewthread.php?tid=6903 PETN-based Cast Explosives] | ||
[[Category:Chemical compounds]] | [[Category:Chemical compounds]] |
Revision as of 16:24, 20 January 2019
Names | |
---|---|
IUPAC name
[3-Nitrooxy-2,2-bis(nitrooxymethyl)propyl] nitrate
| |
Other names
Pentaerythrityl tetranitrate
Pentrite Pentrit | |
Identifiers | |
Jmol-3D images | Image |
| |
Properties | |
C5H8N4O12 | |
Molar mass | 316.14 g/mol |
Appearance | White crystalline solid |
Density | 1.77 g/cm3 (at 20 °C) |
Melting point | 141.3 °C (286.3 °F; 414.4 K) |
Boiling point | 180 °C (356 °F; 453 K) (decomp. begins > 150 °C) |
0.0043 mg/100 mL (at 20 °C)[1] | |
Solubility | Very soluble in acetone Soluble in benzene, toluene Slightly soluble in methanol |
Solubility in acetone | 25.4 g/100 g (20 °C) |
Solubility in ethyl acetate | 10.619 g/100 g |
Hazards | |
Safety data sheet | detotec |
Related compounds | |
Related compounds
|
Erythritol tetranitrate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Pentaerythritol tetranitrate or PETN is an explosive material, widely used in military applications, mainly due to its good stability and general performances. It is a nitrated organic compound, with the chemical formula C5H8N4O12.
Contents
Properties
Chemical
PETN will burn if ignited in air, releasing carbon dioxide, water vapor and soot.
PETN does not hydrolyze in water at room temperature, though this changes at high temperatures.
Physical
PETN is a white crystalline solid, insoluble in water, but soluble in acetone and dimethylformamide (40 g/100 g at 40 °C), as well as benzene and toluene. It also shows good solubility in ethyl acetate (10.619 g/100 g EtOAc).[2] It is also slightly soluble in alcohols, such as methanol and ethanol.
Explosive
Pentaerythritol tetranitrate is one of the most powerful explosive materials known, with a relative effectiveness (RE) factor of 1.66.
PETN is rarely used as a pure compound in explosive devices, instead it is mixed with various plasticizers, to form plastic explosives. When mixed with with RDX, binders (styrene-butadiene e.g.), plasticizers (such as n-octyl phthalate or tributyl citrate), antioxidants (N-phenyl-2-naphthylamine) and dyes (Sudan I or IV) it forms a very powerful plastic explosive called Semtex, widely used by various countries of the former Soviet block.
PETN is more difficult to detonate than primary explosives: dropping or igniting a block of PETN will not result in an explosion (at atmospheric pressure it is difficult to ignite and burns slow), however it is more sensitive to shock and friction than other secondary explosives such as TNT or tetryl.
Availability
PETN is sold in pharmacies as a vasodilator, as treatment for heart conditions. The heart medicine Lentonitrat is nearly pure PETN.
Preparation
PETN can be prepared by nitrating pentaerythritol using concentrated nitric acid under controlled conditions.[3]
Projects
- Make blasting charges
- Heart medication
Handling
Safety
PETN is a vasoldilator and ingestion should be avoided.
Storage
PETN should be stored in closed containers. Urea is sometimes added as a stabilizer.
Disposal
PETN can be safely neutralized with Fenton's reagent. Diluted solutions of PETN should be added slowly, to prevent splashing.
Powdered iron can be used as a reducing agent.[4]
References
- ↑ Clayton, G. D. and F. E. Clayton (eds.). Patty's Industrial Hygiene and Toxicology: Volume 2A, 2B, 2C: Toxicology. 3rd ed. New York: John Wiley Sons, 1981-1982., p. 4195
- ↑ http://pubs.acs.org/doi/abs/10.1021/j150566a032
- ↑ http://www.google.com/patents/US2370437
- ↑ http://pubs.acs.org/doi/abs/10.1021/es7029703?journalCode=esthag
Relevant Sciencemadness threads
- Chemical pages without CAS Registry Number
- Articles without EBI source
- Chemical pages without ChemSpiderID
- Chemical pages without DrugBank identifier
- Articles without KEGG source
- Articles without InChI source
- Articles without UNII source
- Articles containing unverified chemical infoboxes
- Chemical compounds
- Organic compounds
- Nitrates
- Nitrated organic compounds
- Energetic materials
- High explosives
- Secondary explosives
- Things that can kill you very quickly