Pentaerythritol Tetranitrate

• Formula: C₅H₈N₄O₁₂
• Molecular weight: 316.1366
• IUPAC Standard InChI: InChI=1S/C5H8N4O12/c10-6(11)18-1-5(2-19-7(12)13,3-20-8(14)15)4-21-9(16)17/h1-4H2 Copy

  
• IUPAC Standard InChIKey: TZRXHJWUDPFEEY-UHFFFAOYSA-N Copy
• CAS Registry Number: 78-11-5
• Chemical structure:
  This structure is also available as a 2d Mol file
• Other names: 1,3-Propanediol, 2,2-bis[(nitrooxy)methyl]-, dinitrate (ester); Angicap; Angitet; Antora; Arcotrate; Baritrate; Cardiacap; CHOT; Deltrate-20; Dilcoran-80; Dipentrate; Duotrate; Erinit; Extex; Hasethrol; Kaytrate; Lentrat; Lowetrate; Martrate-45; Metranil; Mycardol; Myotrate 10; Neo-Corovas; Neopentanetetrayl nitrate; Niperyt; Niperyth; Nitrinal; Nitro-Riletten; Nitropent; Nitropenta; Nitropenta 7W; Nitropentaerythrite; Nitropentaerythritol; Nitropenton; Nitrotalans; Pen-Tetra; Pencard; Pentaerythrityl tetranitrate; Pentafin; Pentanitrine; Pentanitrol; Pentestan-80; Pentetrate Unicelles; Penthrit; Penthrite; Pentitrate; Pentral 80; Pentrate; Pentrinat; Pentrite; Pentritol; Pentryate; Pergitral; Peridex; Peridex-LA; Peritrate; Perityl; Prevangor; PETN; Quintrate; Rythritol; Subicard; Tanipent; Tentrate-20; Tetranitropentaerythrite; Tetranitropentaerythritol; Tetrasule; Tranite D-Lay; TEN; Vaso-80 Unicelles; Vasodiatol; Vasolat; XTX 8003; 2,2-Bis(Hydroxymethyl)-1,3-propanediol tetranitrate; 1,3-Propanediol, 2,2-bis[(nitrooxy)methyl]-, dinitrate; P.E.T.N.; Pentaerithrityl Tetranitrate; 2,2-Bis[(nitrooxy)methyl]-1,3-propanediol dinitrate (ester); Pentafilin; Pentritol tempules; Terpate; 1,3-Propanediol, 2,2-bis((nitrooxy)methyl)-, 1,3-dinitrate; Tena; C 2; C 2 (explosive); Nitrine; Nitrolong
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• Information on this page:
  • Condensed phase thermochemistry data
  • Phase change data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • References
  • Notes
• Other data available:
  • Gas Chromatography
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Condensed phase thermochemistry data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Phase change data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled as indicated in comments:
AC - William E. Acree, Jr., James S. Chickos
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Enthalpy of sublimation

IR Spectrum

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Coblentz Society, Inc.

Condensed Phase Spectrum

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Notice: Except where noted, spectra from this collection were measured on dispersive instruments, often in carefully selected solvents, and hence may differ in detail from measurements on FTIR instruments or in other chemical environments. More information on the manner in which spectra in this collection were collected can be found here.

Notice: Concentration information is not available for this spectrum and, therefore, molar absorptivity values cannot be derived.

Additional Data

Mass spectrum (electron ionization)

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Spectrum

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Additional Data

References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Ornellas, Carpenter, et al., 1966
Ornellas, D.L.; Carpenter, J.H.; Gunn, S.R., Detonation calorimeter and results obtained with pentaerythritol tetranitrate (PETN), Rev. Sci. Instrum., 1966, 37, 907-912. [all data]

Burlot, 1939
Burlot, E., Etude relative a la calorimetrie des explosifs, Mem. Poudres, 1939, 29, 226-260. [all data]

Cox and Pilcher, 1970
Cox, J.D.; Pilcher, G., Thermochemistry of Organic and Organometallic Compounds, Academic Press, New York, 1970, 1-636. [all data]

Cundall, Frank Palmer, et al., 1978
Cundall, Robert B.; Frank Palmer, T.; Wood, Colin E.C., Vapour pressure measurements on some organic high explosives, J. Chem. Soc., Faraday Trans. 1, 1978, 74, 0, 1339, https://doi.org/10.1039/f19787401339 . [all data]

Edwards, 1953
Edwards, G., The vapour pressure of cyclo-trimethylenetrinitramine (cyclonite) and pentaerythritoltetranitrate, Trans. Faraday Soc., 1953, 49, 152. [all data]

Lau, Hildenbrand, et al., 2004
Lau, Kai H.; Hildenbrand, Donald L.; Crouch-Baker, Steven; Sanjurjo, Angel, Sublimation Pressure and Vapor Molecular Weight of Pentaerythritol Tetranitrate, J. Chem. Eng. Data, 2004, 49, 3, 544-546, https://doi.org/10.1021/je0302203 . [all data]

Jones, 1960
Jones, A.H., Sublimation Pressure Data for Organic Compounds., J. Chem. Eng. Data, 1960, 5, 2, 196-200, https://doi.org/10.1021/je60006a019 . [all data]

Cox and Pilcher, 1970, 2
Cox, J.D.; Pilcher, G., Thermochemistry of Organic and Organometallic Compounds, Academic Press Inc., London, 1970, 643. [all data]

Notes

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• Symbols used in this document:
  

  ΔcH°solid	Enthalpy of combustion of solid at standard conditions
  ΔfH°solid	Enthalpy of formation of solid at standard conditions
  ΔsubH	Enthalpy of sublimation
  ΔsubH°	Enthalpy of sublimation at standard conditions

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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