Butanoic acid, butyl ester

• Formula: C₈H₁₆O₂
• Molecular weight: 144.2114
• IUPAC Standard InChI: InChI=1S/C8H16O2/c1-3-5-7-10-8(9)6-4-2/h3-7H2,1-2H3 Copy

  
• IUPAC Standard InChIKey: XUPYJHCZDLZNFP-UHFFFAOYSA-N Copy
• CAS Registry Number: 109-21-7
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Isotopologues:
  • butyl butanoate-d3
  • butyl-d3 butanoate
  • butyl-d3 butanoate-d3
• Other names: Butyric acid, butyl ester; n-Butyl butanoate; n-Butyl butyrate; n-Butyl n-butyrate; Butyl butanoate; Butyl butylate; Butyl butyrate; 1-Butyl butyrate; Butyl n-butyrate; n-Butyl n-butanoate; n-Butyric acid n-butyl ester; Butyl ester of butanoic acid; NSC 8458
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • Phase change data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
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  • 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

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

Aldrich Chemical Company Inc., 1990
Aldrich Chemical Company Inc., Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 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]

Cymerman-Craig and Horning, 1960
Cymerman-Craig; Horning, J. Org. Chem., 1960, 25, 2098. [all data]

Hoffmann, 1959
Hoffmann, W.L., Riechst. Aromen, 1959, 9, 273. [all data]

Bachman and Vogt, 1958
Bachman, G.B.; Vogt, C.M., J. Am. Chem. Soc., 1958, 80, 2987. [all data]

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

Natta, Pino, et al., 1950
Natta, G.; Pino, P.; Mantica, E., Gazz. Chim. Ital., 1950, 80, 680. [all data]

Lecat, 1943
Lecat, M., Azeotropes of Ethyl Urethane and other Azeotropes, C. R. Hebd. Seances Acad. Sci., 1943, 217, 273. [all data]

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

Grignard and Fluchaire, 1928
Grignard, V.; Fluchaire, M., Suiz les proprietetes condensantes des alcoolates magnesiens mixtures, Ann. Chim. (Paris), 1928, 9, 5. [all data]

Timmermans, 1927
Timmermans, J., The Melting Point of Organic Substances, Bull. Soc. Chim. Belg., 1927, 36, 502. [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]

Lievens, 1924
Lievens, G., The freezing point of organic substances: viii esters containing a normal c(5) radical, Bull. Soc. Chim. Belg., 1924, 33, 122-131. [all data]

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

Gartenmeister, 1886
Gartenmeister, R., Investigation of the physical characterstics of liquid compounds: vi boiling point and specific volume of normal fatty acid esters, Justus Liebigs Ann. Chem., 1886, 233, 249-315. [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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