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Quinoline, 2-methyl-

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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, Kenneth Kroenlein director

Tboil (K) Reference Comment
521.2Aldrich Chemical Company Inc., 1990BS
520.90Zegalska, 1968Uncertainty assigned by TRC = 0.17 K; TRC
521.15Cooper, Crowne, et al., 1967Uncertainty assigned by TRC = 0.7 K; TRC
520.9Malanowski, 1961Uncertainty assigned by TRC = 0.07 K; TRC
519.8Rampolla and Smyth, 1958Uncertainty assigned by TRC = 0.3 K; TRC
520.Zalukajevs and Bankovski, 1955Uncertainty assigned by TRC = 10. K; TRC
519.Ardashev, 1949Uncertainty assigned by TRC = 6. K; TRC
519.95Lecat, 1947Uncertainty assigned by TRC = 0.6 K; TRC
520.15Hackmann, Wibaut, et al., 1943Uncertainty assigned by TRC = 2. K; TRC
518.95Rau and Narayanaswamy, 1934Uncertainty assigned by TRC = 0.4 K; TRC
519.Rabinovich and Dzirkal, 1933Uncertainty assigned by TRC = 5. K; TRC
520.35Harris and Pope, 1922Uncertainty assigned by TRC = 0.6 K; TRC

In addition to the Thermodynamics Research Center (TRC) data available from this site, much more physical and chemical property data is available from the following TRC products:


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]

Zegalska, 1968
Zegalska, B., Liquid-Solid Equilibria in Binary Systems Formed by Quinoline, Bull. Acad. Pol. Sci., Ser. Sci. Chim., 1968, 16, 335-41. [all data]

Cooper, Crowne, et al., 1967
Cooper, A.R.; Crowne, C.W.P.; Farrell, P.G., Gas-Liquid Chromatographic Studies of Electron-Donor-Acceptor Systems, Trans. Faraday Soc., 1967, 63, 447. [all data]

Malanowski, 1961
Malanowski, S., Vapour-liquid equilibria of quinoline bases in binary systems quinoline + isoquinoline and isoquinoline + quinaldine, Bull. Acad. Pol. Sci., Ser. Sci. Chim., 1961, 9, 77-82. [all data]

Rampolla and Smyth, 1958
Rampolla, R.W.; Smyth, C.P., J. Am. Chem. Soc., 1958, 80, 1057. [all data]

Zalukajevs and Bankovski, 1955
Zalukajevs, L.; Bankovski, J., Acid-less method of preparation of quinaldine., Dokl. Akad. Nauk SSSR, 1955, 100, 705-6. [all data]

Ardashev, 1949
Ardashev, B.I., Quinoline derivatives. V. Simultaneous condensation of aromatic amines and ethylene glycol with acetone or methyl ethyl ketone., Zh. Obshch. Khim., 1949, 19, 1656-63. [all data]

Lecat, 1947
Lecat, M., Some azeotropes of which one constituant is heterocyclic nitrogen, Ann. Soc. Sci. Bruxelles, Ser. 1, 1947, 61, 73. [all data]

Hackmann, Wibaut, et al., 1943
Hackmann, J.Th.; Wibaut, J.P.; Gitsels, H.P.L., Basic N compounds from cracked distillates of California petroleum, Recl. Trav. Chim. Pays-Bas, 1943, 62, 229. [all data]

Rau and Narayanaswamy, 1934
Rau, M.A.G.; Narayanaswamy, B.N., The determination of dipole moments using the method of diluted solutions: I and II, Z. Phys. Chem., Abt. B, 1934, 26, 23. [all data]

Rabinovich and Dzirkal, 1933
Rabinovich, P.N.; Dzirkal, V.K., Simplified preparation of some organic compounds. IV. quinaldine., Khim.-Farm. Prom-st., 1933, 273. [all data]

Harris and Pope, 1922
Harris, J.E.G.; Pope, W.M.J., Isoquinoline and the Isoquinoline-Reds, J. Chem. Soc., 1922, 121, 1029. [all data]


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