Quinoline
- Formula: C9H7N
- Molecular weight: 129.1586
- IUPAC Standard InChIKey: SMWDFEZZVXVKRB-UHFFFAOYSA-N
- CAS Registry Number: 91-22-5
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
View 3d structure (requires JavaScript / HTML 5) - Other names: B 500; Benzopyridine; Benzo[b]Pyridine; Leucol; Leukol; Quinolin; 1-Azanaphthalene; 1-Benzazine; Chinoline; Chinoleine; Chinolin; Leucoline; USAF EK-218; UN 2656; NSC 3396
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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 |
---|---|---|
511.2 | Weast and Grasselli, 1989 | BS |
510.55 | Sundaram, 1969 | Uncertainty assigned by TRC = 0.4 K; TRC |
510.80 | Zegalska, 1968 | Uncertainty assigned by TRC = 0.15 K; TRC |
510.25 | Cooper, Crowne, et al., 1967 | Uncertainty assigned by TRC = 0.6 K; TRC |
510.57 | Maczynski and Maczynska, 1965 | Uncertainty assigned by TRC = 0.15 K; TRC |
510.78 | Malanowski, 1961 | Uncertainty assigned by TRC = 0.07 K; TRC |
509.15 | Tschamler and Krischai, 1951 | Uncertainty assigned by TRC = 1.5 K; TRC |
510.45 | Lecat, 1947 | Uncertainty assigned by TRC = 0.6 K; TRC |
508.15 | Hackmann, Wibaut, et al., 1943 | Uncertainty assigned by TRC = 2. K; TRC |
510.45 | Lecat, 1943 | Uncertainty assigned by TRC = 0.3 K; TRC |
510.55 | Lecat, 1943, 2 | Uncertainty assigned by TRC = 0.4 K; TRC |
510.25 | Timmermans and Hennaut-Roland, 1937 | Uncertainty assigned by TRC = 0.4 K; TRC |
511.15 | Earp and Glasstone, 1935 | Uncertainty assigned by TRC = 1. K; TRC |
511.15 | Grimm and Patrick, 1923 | Uncertainty assigned by TRC = 1.5 K; TRC |
509.65 | Harris and Pope, 1922 | Uncertainty assigned by TRC = 0.6 K; TRC |
511.15 | Timmermans, 1911 | Uncertainty assigned by TRC = 0.5 K; TRC |
511.15 | Perkin, 1896 | Uncertainty assigned by TRC = 1. K; TRC |
511.15 | Kahlbaum, 1884 | Uncertainty assigned by TRC = 2. 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]
Sundaram, 1969
Sundaram, K.M.S.,
Viscosity, density, refractive index, electrical conductivity, and surface tension of quinoline-acetic acid mixtures,
Z. Phys. Chem. (Leipzig), 1969, 241, 107. [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]
Maczynski and Maczynska, 1965
Maczynski, A.; Maczynska, Z.,
Vapour-liquid equilibra in binary system quinoline-water,
Bull. Acad. Pol. Sci., Ser. Sci. Chim., 1965, 13, 299. [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]
Tschamler and Krischai, 1951
Tschamler, H.; Krischai, H.,
Binary liquid mixtures: XV. Quinoline + m-cresol, a strongly neg. system,
Monatsh. Chem., 1951, 82, 259. [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]
Lecat, 1943
Lecat, M.,
Negative and other Azeotropes,
C. R. Hebd. Seances Acad. Sci., 1943, 217, 242. [all data]
Lecat, 1943, 2
Lecat, M.,
Azeotropes of Ethyl Urethane and other Azeotropes,
C. R. Hebd. Seances Acad. Sci., 1943, 217, 273. [all data]
Timmermans and Hennaut-Roland, 1937
Timmermans, J.; Hennaut-Roland, M.,
Works from International Bureau at Physical-Chemical Standards. VIII. Physical constants of 20 organic compounds,
J. Chim. Phys. Phys.-Chim. Biol., 1937, 34, 693. [all data]
Earp and Glasstone, 1935
Earp, D.P.; Glasstone, S.,
Dielectric polarisation and molecular-compound formation in solution,
J. Chem. Soc., 1935, 1935, 1709. [all data]
Grimm and Patrick, 1923
Grimm, F.V.; Patrick, W.A.,
The Dielectric Constastants of Organic Liquids at the Boilin Point,
J. Am. Chem. Soc., 1923, 45, 2794. [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]
Timmermans, 1911
Timmermans, J.,
Researches on the freezing point of organic liquid compounds,
Bull. Soc. Chim. Belg., 1911, 25, 300. [all data]
Perkin, 1896
Perkin, W.H.,
LXIX. On Magnetic Rotatory Power, especially of Aromatic Compounds,
J. Chem. Soc., 1896, 69, 1025-1257. [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]
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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