Pentanal

• Formula: C₅H₁₀O
• Molecular weight: 86.1323
• IUPAC Standard InChI: InChI=1S/C5H10O/c1-2-3-4-5-6/h5H,2-4H2,1H3 Copy

  
• IUPAC Standard InChIKey: HGBOYTHUEUWSSQ-UHFFFAOYSA-N Copy
• CAS Registry Number: 110-62-3
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Other names: Valeraldehyde; n-Pentanal; n-Valeraldehyde; Valeral; Valerianic aldehyde; Valeric acid aldehyde; Valeric aldehyde; Valeryl aldehyde; n-C4H9CHO; Amyl aldehyde; Butyl formal; UN 2058; n-Valeric aldehyde; 1-Pentanal; Pentan-1-al; NSC 35404; Pentylaldehyde; pentanal (valeraldehyde); valderaldehyde
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
  • Phase change data
  • Reaction thermochemistry data
  • Henry's Law data
  • Gas phase ion energetics data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
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Normal boiling point

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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:
BS - Robert L. Brown and Stephen E. Stein
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

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.

Weast and Grasselli, 1989
CRC Handbook of Data on Organic Compounds, 2nd Editon, Weast,R.C and Grasselli, J.G., ed(s)., CRC Press, Inc., Boca Raton, FL, 1989, 1. [all data]

Markovnik, Sachek, et al., 1979
Markovnik, V.S.; Sachek, A.I.; Peshchenko, A.D.; Shvaro, O.V.; Andreevskii, D.N.; Olizarevich, N.M., Termodin. Org. Soedin., 1979, 107. [all data]

Gaiffe and Palland, 1962
Gaiffe, A.; Palland, R., C. R. Hebd. Seances Acad. Sci., 1962, 254, 496. [all data]

Sisti, Burgmaster, et al., 1962
Sisti, A.J.; Burgmaster, J.; Fudim, M., J. Org. Chem., 1962, 27, 279. [all data]

Hickey, 1948
Hickey, M.J., J. Org. Chem., 1948, 13, 443. [all data]

Schniepp and Geller, 1945
Schniepp, L.E.; Geller, H.H., J. Am. Chem. Soc., 1945, 67, 54. [all data]

Prevost, 1944
Prevost, C., Bull. Soc. Chim. Fr., 1944, 11, 218. [all data]

Komarewsky and Kritchevsky, 1943
Komarewsky, V.I.; Kritchevsky, T.H., Synthesis of Olefin Hydrocarbons by Catalytic Condensation and Dehydration of Aliphatic Aldehydes, J. Am. Chem. Soc., 1943, 65, 547-8. [all data]

Coomber and Partington, 1938
Coomber, D.I.; Partington, J.R., Studies in dielectric polarisation part xxiii the dipole moments of some aliphatic and aromatic aldehydes and of anthrone, J. Chem. Soc., 1938, 1938, 1444. [all data]

Kuhn and Grundmann, 1937
Kuhn, R.; Grundmann, C., Chem. Ber., 1937, 70, 1894. [all data]

Swan and Field, 1937
Swan, S.; Field, E.W., Trans. Electrochem. Soc., 1937, 72, 327. [all data]

Kohlraush and Koppl, 1934
Kohlraush, K.W.F.; Koppl, F., Z. Phys. Chem., Abt. B, 1934, 24, 370. [all data]

Whitmore and Church, 1933
Whitmore, F.C.; Church, J.M., J. Am. Chem. Soc., 1933, 55, 1119. [all data]

Bruylants, 1931
Bruylants, P., Contribution to the study of ethylene nitriles beta-ethyl-crotonic nitrile, Bull. Cl. Sci., Acad. R. Belg., 1931, 17, 1008. [all data]

Simon, 1929
Simon, I., Freezing Temperature of Organic Compounds. XI. Compounds in C5 and C6., Bull. Soc. Chim. Belg., 1929, 38, 47-70. [all data]

Parnas, 1910
Parnas, J., Biochem. Z., 1910, 28, 274. [all data]

Blaise, 1904
Blaise, E.E., Bull. Soc. Chim. Fr., 1904, 31, 483. [all data]

Zander, 1884
Zander, A., The specific volumes of liquid compounds: IV normal fatty acids and normal fatty alcohols, Justus Liebigs Ann. Chem., 1884, 224, 56-95. [all data]

Lieben and Rossi, 1871
Lieben, A.; Rossi, A., Justus Liebigs Ann. Chem., 1871, 159, 58. [all data]

Notes

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• Symbols used in this document:
  

  Tboil

  Boiling point

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