n-Propyl acetate
- Formula: C5H10O2
- Molecular weight: 102.1317
- IUPAC Standard InChIKey: YKYONYBAUNKHLG-UHFFFAOYSA-N
- CAS Registry Number: 109-60-4
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
The 3d structure may be viewed using Java or Javascript. - Other names: Acetic acid, propyl ester; Propyl acetate; 1-Acetoxypropane; 1-Propyl acetate; CH3COOCH2CH2CH3; Acetic acid n-propyl ester; n-Propyl ethanoate; Acetate de propyle normal; Octan propylu; Propyl ethanoate; Propylester kyseliny octove; UN 1276; Propyl ester of acetic acid; NSC 72025; n-Propanol acetate
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Normal boiling point
Go To: Top, References, Notes
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
Tboil (K) | Reference | Comment |
---|---|---|
374.8 | Weast and Grasselli, 1989 | BS |
374. | American Tokyo Kasei, 1988 | BS |
374.7 | Majer and Svoboda, 1985 | |
374.7 | Svoboda, Vesely, et al., 1977 | Uncertainty assigned by TRC = 0.3 K; TRC |
374.28 | Geiseler, Quitzsch, et al., 1973 | Uncertainty assigned by TRC = 0.2 K; TRC |
374.62 | Polak and Mertl, 1965 | Uncertainty assigned by TRC = 0.5 K; TRC |
374.2 | Scheer, Koogman, et al., 1963 | Uncertainty assigned by TRC = 2. K; TRC |
374.85 | Timmermans and Hennaut-Roland, 1959 | Uncertainty assigned by TRC = 0.5 K; TRC |
374.75 | Miller, 1958 | Uncertainty assigned by TRC = 0.5 K; TRC |
373.9 | Hoffmann and Weiss, 1957 | Uncertainty assigned by TRC = 1. K; TRC |
372.65 | Emmons and Lucas, 1955 | Uncertainty assigned by TRC = 1. K; TRC; Data excluded from overall average |
374.83 | Gjaldbaek and Andersen, 1954 | Uncertainty assigned by TRC = 0.3 K; TRC |
374.5 | Wetzel, Miller, et al., 1953 | Uncertainty assigned by TRC = 1. K; TRC |
370.65 | Schreyer, 1952 | Uncertainty assigned by TRC = 1. K; TRC; Data excluded from overall average |
374.75 | Mumford and Phillips, 1950 | Uncertainty assigned by TRC = 1. K; TRC |
374.75 | French, 1947 | Uncertainty assigned by TRC = 1. K; TRC |
374.690 | Wojciechowski and Smith, 1937 | Uncertainty assigned by TRC = 0.08 K; TRC |
375. | Gill and Dexter, 1934 | Uncertainty assigned by TRC = 3. K; TRC |
374.75 | Lecat, 1927 | Uncertainty assigned by TRC = 0.5 K; TRC |
374.8 | Lecat, 1927, 2 | Uncertainty assigned by TRC = 0.5 K; TRC |
374.8 | Hannotte, 1926 | Uncertainty assigned by TRC = 0.4 K; TRC |
374.8 | Lecat, 1926 | Uncertainty assigned by TRC = 0.5 K; TRC |
374.75 | Lecat, 1926, 2 | Uncertainty assigned by TRC = 1. K; TRC |
374.62 | Mathews, 1926 | Uncertainty assigned by TRC = 1. K; TRC |
375.15 | Munch, 1926 | Uncertainty assigned by TRC = 1. K; TRC |
373.65 | Smith and Boord, 1926 | Uncertainty assigned by TRC = 1. K; TRC |
373.95 | Timmermans and Mattaar, 1921 | Uncertainty assigned by TRC = 0.5 K; TRC |
374.7 | Young, 1910 | Uncertainty assigned by TRC = 1. K; TRC |
375.3 | Guttman, 1907 | Uncertainty assigned by TRC = 1. K; TRC |
374.7 | Young and Thomas, 1893 | Uncertainty assigned by TRC = 0.5 K; TRC |
373. | Landolt and Jahn, 1892 | Uncertainty assigned by TRC = 2. K; TRC; Data excluded from overall average |
375.0 | Gartenmeister, 1886 | Uncertainty assigned by TRC = 1.5 K; TRC |
373.95 | Kahlbaum, 1884 | Uncertainty assigned by TRC = 1. K; TRC |
375.65 | Perkin, 1884 | Uncertainty assigned by TRC = 1. K; TRC |
375.2 | Von Reis, 1881 | Uncertainty assigned by TRC = 0.7 K; TRC |
371. | Bruhl, 1880 | Uncertainty assigned by TRC = 3. K; TRC; Data excluded from overall average |
375.13 | Linnemann and von Zotta, 1872 | Uncertainty assigned by TRC = 1. K; TRC |
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]
Majer and Svoboda, 1985
Majer, V.; Svoboda, V.,
Enthalpies of Vaporization of Organic Compounds: A Critical Review and Data Compilation, Blackwell Scientific Publications, Oxford, 1985, 300. [all data]
Svoboda, Vesely, et al., 1977
Svoboda, V.; Vesely, F.; Holub, R.; Pick, J.,
Heats of vaporization of alkyl acetates and propionates,
Collect. Czech. Chem. Commun., 1977, 42, 943-51. [all data]
Geiseler, Quitzsch, et al., 1973
Geiseler, G.; Quitzsch, K.; Hofmann, H.-P.; Pfestorf, R.Z.,
Z. Phys. Chem. (Leipzig), 1973, 252, 170. [all data]
Polak and Mertl, 1965
Polak, J.; Mertl, I.,
Saturated vapor pressure of methyl acetate, ethyl acetate, n-propyl acetate, methyl propionate and ethyl propionate,
Collect. Czech. Chem. Commun., 1965, 30, 3526-8. [all data]
Scheer, Koogman, et al., 1963
Scheer, J.C.; Koogman, E.C.; Sixma, F.L.J.,
Gas Phase Pyrolysis of Alkyl Acetates,
Recl. Trav. Chim. Pays-Bas, 1963, 82, 1123. [all data]
Timmermans and Hennaut-Roland, 1959
Timmermans, J.; Hennaut-Roland, M.,
Work of the International Bureau of Physico-Chemical Properties physical constants of twenty organic compounds,
J. Chim. Phys. Phys.-Chim. Biol., 1959, 56, 984-1023. [all data]
Miller, 1958
Miller, K.J.,
Boiling Point-Composition Diagrams for the Systems 2-Ethoxyethanol- Ethyl Acetate and 2-Ethoxyethanol-Propyl Acetate,
Chem. Eng. Data Ser., 1958, 3, 239-40. [all data]
Hoffmann and Weiss, 1957
Hoffmann, F.W.; Weiss, J.M.,
J. Am. Chem. Soc., 1957, 79, 4759. [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]
Gjaldbaek and Andersen, 1954
Gjaldbaek, J. Chr.; Andersen, E.K.,
The Solubility of Carbon Dioxide, Oxygen, Carbon Monoxide and Nitrogen in Polar Solvents,
Acta Chem. Scand., 1954, 8, 1398. [all data]
Wetzel, Miller, et al., 1953
Wetzel, F.H.; Miller, J.G.; Day, A.R.,
Effect of Structure on Reactivity VII. The Energies of Activation and the Entropy of Activation for Ammonolysis of Esters,
J. Am. Chem. Soc., 1953, 75, 1150. [all data]
Schreyer, 1952
Schreyer, R.C.,
Synthesis of Esters from Olefins, Hydrogen, Carbon Monoxide and Acetic Acid,
J. Am. Chem. Soc., 1952, 74, 3242. [all data]
Mumford and Phillips, 1950
Mumford, S.A.; Phillips, J.W.C.,
19. The Physical Properties of Some Aliphatic Compounds,
J. Chem. Soc., 1950, 1950, 75-84. [all data]
French, 1947
French, C.M.,
Trans. Faraday Soc., 1947, 43, 356. [all data]
Wojciechowski and Smith, 1937
Wojciechowski, M.; Smith, E.R.,
Boiling Points and Densities of Acetates of Normal Aliphatic Alcohols,
J. Res. Natl. Bur. Stand. (U. S.), 1937, 18, 499. [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: 7th list,
Ann. Soc. Sci. Bruxelles, Ser. B, 1927, 47, 108-14. [all data]
Lecat, 1927, 2
Lecat, M.,
New binary azeotropes: 6th list,
Ann. Soc. Sci. Bruxelles, Ser. B, 1927, 47, 63-71. [all data]
Hannotte, 1926
Hannotte, T.,
Azeotropic Properties of Formic Ethers and Acetates of Saturated Aliphatic Alcohols,
Bull. Soc. Chim. Belg., 1926, 35, 86. [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]
Mathews, 1926
Mathews, J.H.,
The Accurate Measurement of Heats of Vaporization of Liquids,
J. Am. Chem. Soc., 1926, 48, 562. [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]
Smith and Boord, 1926
Smith, A.W.; Boord, C.E.,
Infra-Red Absorption in Ethers, Esters, and Related Substances,
J. Am. Chem. Soc., 1926, 48, 1512. [all data]
Timmermans and Mattaar, 1921
Timmermans, J.; Mattaar, J.F.,
Freezing points of orgainic substances VI. New experimental determinations.,
Bull. Soc. Chim. Belg., 1921, 30, 213. [all data]
Young, 1910
Young, S.,
The Internal Heat of Vaporization constants of thirty pure substances,
Sci. Proc. R. Dublin Soc., 1910, 12, 374. [all data]
Guttman, 1907
Guttman, L.F.,
The determination of melting points at low temperatures: II.,
J. Am. Chem. Soc., 1907, 29, 345-9. [all data]
Young and Thomas, 1893
Young, S.; Thomas, G.L.,
The vapour pressures, molecular volumes, and critical constants of ten of the lower esters,
J. Chem. Soc., 1893, 63, 1191. [all data]
Landolt and Jahn, 1892
Landolt, H.; Jahn, H.,
The Molecular Refraction of Several Simple Organic Compounds for Rays of Infinitely Great Wave Length.,
Z. Phys. Chem., Stoechiom. Verwandtschaftsl., 1892, 10, 289. [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]
Kahlbaum, 1884
Kahlbaum, G.W.A.,
The dependence of Boiling Temperature on Air Pressure,
Ber. Dtsch. Chem. Ges., 1884, 17, 1245. [all data]
Perkin, 1884
Perkin, W.H.,
On the Magnetic Rotary Polarisation of Compounds in Relation to their Chemical Consitution; with Observations on the Preparation and Relative Densities of the Bodies Examined,
J. Chem. Soc., 1884, 45, 421-580. [all data]
Von Reis, 1881
Von Reis, M.A.,
IV. The Specific Heat of Liquid Organic Compounds and its Relation to Molecular Weight.,
Ann. Phys. (Leipzig), 1881, 13, 447. [all data]
Bruhl, 1880
Bruhl, J.W.,
The Chemical Constitution of Organic Compounds in Relation to Their Density and Their Light Propagating Ability,
Justus Liebigs Ann. Chem., 1880, 200, 139-231. [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
Go To: Top, Normal boiling point, References
- Symbols used in this document:
Tboil Boiling point - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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