Acetic acid, pentyl ester
- Formula: C7H14O2
- Molecular weight: 130.1849
- IUPAC Standard InChIKey: PGMYKACGEOXYJE-UHFFFAOYSA-N
- CAS Registry Number: 628-63-7
- 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. - Isotopologues:
- Other names: n-Amyl acetate; n-Pentyl acetate; Amyl acetate; Birnenoel; Pentyl acetate; Acetic acid, amyl ester; Amyl acetic ester; Amyl acetic ether; Banana oil; Pear oil; Pent-acetate; 1-Pentanol acetate; 1-Pentyl acetate; Acetic acid n-amyl ester; n-Pentyl ethanoate; Acetate d'amyle; Amylazetat; Octan amylu; Pent-acetate 28; Amylester kyseliny octove; Primary amyl acetate; Pentyl ester of acetic acid; Acetic acid, n-pentyl ester; 1-Acetoxypentane; NSC 7923
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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
Tboil (K) | Reference | Comment |
---|---|---|
418.7 | Aldrich Chemical Company Inc., 1990 | BS |
422.4 | Weast and Grasselli, 1989 | BS |
421. | American Tokyo Kasei, 1988 | BS |
420.4 | Kal'nitskaya, Komarova, et al., 1977 | Uncertainty assigned by TRC = 0.5 K; TRC |
421. | Nayanov, Zorin, et al., 1976 | Uncertainty assigned by TRC = 2. K; TRC |
422.1 | Fahmy and El-Ghannam, 1972 | Uncertainty assigned by TRC = 1. K; TRC |
422.2 | Shlenkina, 1971 | Uncertainty assigned by TRC = 1.5 K; TRC |
420. | Sun and Connors, 1969 | Uncertainty assigned by TRC = 3. K; TRC |
422.4 | Scheer, Koogman, et al., 1963 | Uncertainty assigned by TRC = 1. K; TRC |
423. | Zhdanov, Dorofeenko, et al., 1962 | Uncertainty assigned by TRC = 4. K; TRC |
422. | Cohen, Borden, et al., 1961 | Uncertainty assigned by TRC = 1.5 K; TRC |
417.15 | Emmons and Lucas, 1955 | Uncertainty assigned by TRC = 1. K; TRC |
422.7 | Timmermans and Hennaut-Roland, 1955 | Uncertainty assigned by TRC = 0.2 K; TRC |
422.35 | Mumford and Phillips, 1950 | Uncertainty assigned by TRC = 1. K; TRC |
422.1 | Geldof and Wibaut, 1948 | Uncertainty assigned by TRC = 1. K; TRC |
421.85 | Lecat, 1943 | Uncertainty assigned by TRC = 0.3 K; TRC |
421.15 | Ewell and Welch, 1941 | Uncertainty assigned by TRC = 1. K; TRC |
421. | Gill and Dexter, 1934 | Uncertainty assigned by TRC = 2. K; TRC |
411.15 | Smith and Boord, 1926 | Uncertainty assigned by TRC = 1. K; TRC |
422.4 | Lievens, 1924 | Uncertainty assigned by TRC = 1. K; TRC |
421.55 | Jaeger, 1917 | Uncertainty assigned by TRC = 1. K; TRC |
410.7 | Holley, 1902 | Uncertainty assigned by TRC = 0.5 K; TRC |
413.8 | Landolt and Jahn, 1892 | Uncertainty assigned by TRC = 1.5 K; TRC |
420.8 | Gartenmeister, 1886 | Uncertainty assigned by TRC = 1.5 K; TRC |
398.15 | Wurtz, 1864 | Uncertainty assigned by TRC = 3. K; TRC; Data excluded from overall average |
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.
Aldrich Chemical Company Inc., 1990
Aldrich Chemical Company Inc.,
Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 1. [all data]
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]
Kal'nitskaya, Komarova, et al., 1977
Kal'nitskaya, A.M.; Komarova, L.F.; Garber, Yu.N.,
Azeotropic Series of aliphatic Alcohols with Acetate Esters,
Zh. Prikl. Khim. (Leningrad), 1977, 50, 1101-5. [all data]
Nayanov, Zorin, et al., 1976
Nayanov, V.P.; Zorin, V.V.; Zlotskii, S.S.; Rakhmankulov, D.L.,
Identification of Cyclic Acetates and Isomeric Esters by Gas-Liquid Chromatography,
Zh. Prikl. Khim. (Leningrad), 1976, 49, 2350. [all data]
Fahmy and El-Ghannam, 1972
Fahmy, A.F.M.; El-Ghannam, N.I.M.,
The boiling temperature-composition behaviour in binary systems of alkanol acetates with entrainers,
Bull. Acad. Pol. Sci., Ser. Sci. Chim., 1972, 20, 101. [all data]
Shlenkina, 1971
Shlenkina, N.G.,
Molecular light scattering by acetic acid solutions in toluene and n- pentyl acetate,
Russ. J. Phys. Chem. (Engl. Transl.), 1971, 45, 327-8. [all data]
Sun and Connors, 1969
Sun, S.-R.; Connors, K.A.,
Identification of Low Molecular Weight Aliphatic Esters from Rates of Hydrolysis,
J. Pharm. Sci., 1969, 58, 1150. [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]
Zhdanov, Dorofeenko, et al., 1962
Zhdanov, Yu.A.; Dorofeenko, G.N.; Korol'chenko, G.A.,
Catalytic Acetylation of Polyhydroxy Compounds in the Presence of Magnesium Perchlorate,
Dokl. Akad. Nauk SSSR, 1962, 144, 1050. [all data]
Cohen, Borden, et al., 1961
Cohen, H.L.; Borden, D.G.; Minsk, L.N.,
Reduction of Polymers Using Complex Metal Hydrides II,
J. Org. Chem., 1961, 26, 1274. [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]
Timmermans and Hennaut-Roland, 1955
Timmermans, J.; Hennaut-Roland, M.,
Work of the International Bureau of Physical-Chemical Standards. IX. The Physical Constants of Twenty Organic Compounds,
J. Chim. Phys. Phys.-Chim. Biol., 1955, 52, 223. [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]
Geldof and Wibaut, 1948
Geldof, H.; Wibaut, J.P.,
Recl. Trav. Chim. Pays-Bas, 1948, 67, 105. [all data]
Lecat, 1943
Lecat, M.,
Azeotropes of Ethyl Urethane and other Azeotropes,
C. R. Hebd. Seances Acad. Sci., 1943, 217, 273. [all data]
Ewell and Welch, 1941
Ewell, R.H.; Welch, L.M.,
Maximum Boiling Mixtures of chloroparaffins with Donor Liquids,
J. Am. Chem. Soc., 1941, 63, 2475. [all data]
Gill and Dexter, 1934
Gill, A.H.; Dexter, F.P.,
Ind. Eng. Chem., 1934, 26, 881. [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]
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]
Jaeger, 1917
Jaeger, F.M.,
Z. Anorg. Allg. Chem., 1917, 101, 130. [all data]
Holley, 1902
Holley, C.D.,
Liquid Mixtures of Minomum Boiling-Point,
J. Am. Chem. Soc., 1902, 24, 448. [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]
Wurtz, 1864
Wurtz, A.,
Ann. Chim. Phys., 1864, [4] 3, 129. [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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