Butanoic acid, propyl ester

• Formula: C₇H₁₄O₂
• Molecular weight: 130.1849
• IUPAC Standard InChI: InChI=1S/C7H14O2/c1-3-5-7(8)9-6-4-2/h3-6H2,1-2H3 Copy

  
• IUPAC Standard InChIKey: HUAZGNHGCJGYNP-UHFFFAOYSA-N Copy
• CAS Registry Number: 105-66-8
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Isotopologues:
  • propyl butanoate-d3
• Other names: Butyric acid, propyl ester; n-Propyl butyrate; n-Propyl n-butyrate; Propyl butanoate; Propyl butyrate; Propyl n-butyrate; n-Butyric acid n-propyl ester; Propylester kyseliny maselne; Propyl ester of butanoic acid; n-Propanol butyrate; propyl bytanoate
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • Phase change data
  • Henry's Law data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
• Data at other public NIST sites:
  • Gas Phase Kinetics Database
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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

Go To: Top, Normal boiling point, Notes

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]

American Tokyo Kasei, 1988
American Tokyo Kasei, TCI American Organic Chemical 88/89 Catalog, American Tokyo Kasei, Portland, OR, 1988, 1610. [all data]

Emmons and Lucas, 1955
Emmons, W.D.; Lucas, G.B., Peroxytrifluoroacetic acid: V the oxidation of ketones to esters, J. Am. Chem. Soc., 1955, 77, 2287. [all data]

Brandstrom, 1950
Brandstrom, A., Ark. Kemi, 1950, 1, 481. [all data]

French, 1947
French, C.M., Trans. Faraday Soc., 1947, 43, 356. [all data]

Gill and Dexter, 1934
Gill, A.H.; Dexter, F.P., Ind. Eng. Chem., 1934, 26, 881. [all data]

Lecat, 1927
Lecat, M., New binary azeotropes: 6th list, Ann. Soc. Sci. Bruxelles, Ser. B, 1927, 47, 63-71. [all data]

Lecat, 1926
Lecat, M., New binary azeotropes: 3rd list, Ann. Soc. Sci. Bruxelles, Ser. B, 1926, 45, 284-94. [all data]

Lecat, 1926, 2
Lecat, M., New binary azeotropes second list, Recl. Trav. Chim. Pays-Bas, 1926, 45, 620-627. [all data]

Munch, 1926
Munch, J.C., The Refractometric Determination of Alcohols and Esters in Aqueous and in Cottonseed Oil Solutions, J. Am. Chem. Soc., 1926, 48, 994-1003. [all data]

Timmermans, 1922
Timmermans, J., Investigation of the Freezing Point of Organic Substances VII, Bull. Soc. Chim. Belg., 1922, 31, 389. [all data]

Bielecki and Henri, 1913
Bielecki, J.; Henri, V., Quantitative study on absorption of ultra-violet rays by monobasic acids and esters of the aliphatic series: II, Ber. Dtsch. Chem. Ges., 1913, 46, 1304. [all data]

Brown, 1903
Brown, J.C., A direct method for determining latent heat of evaporation, J. Chem. Soc., Trans., 1903, 83, 987. [all data]

Linnemann and von Zotta, 1872
Linnemann, E.; von Zotta, V., Reduction of Formic Acid to Formaldehyde and Methyl Alcohol, Justus Liebigs Ann. Chem., 1872, 161, 15. [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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