Quinoline, 4,6-dimethyl-

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Phase change data

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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

Quantity Value Units Method Reference Comment
Tboil546.7KN/AWeast and Grasselli, 1989BS
Tboil548.KN/AArdashev, 1960Uncertainty assigned by TRC = 5. K; TRC
Tboil546.KN/AArdashev, 1960Uncertainty assigned by TRC = 4. K; TRC
Tboil548.KN/AArdashev and Tertov, 1957Uncertainty assigned by TRC = 6. K; TRC

Reduced pressure boiling point

Tboil (K) Pressure (atm) Reference Comment
413.20.016Weast and Grasselli, 1989BS

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:


Gas Chromatography

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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 by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Kovats' RI, non-polar column, isothermal

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Column type Active phase Temperature (C) I Reference Comment
CapillaryOV-101140.1472.Berlizov, Nabivach, et al., 1987N2; Column length: 50. m; Column diameter: 0.22 mm
CapillaryOV-101160.1487.Berlizov, Nabivach, et al., 1987N2; Column length: 50. m; Column diameter: 0.22 mm

Kovats' RI, polar column, isothermal

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Column type Active phase Temperature (C) I Reference Comment
CapillaryPEG-20M140.2133.Berlizov, Nabivach, et al., 1987N2; Column length: 30. m; Column diameter: 0.25 mm
CapillaryPEG-20M160.2159.Berlizov, Nabivach, et al., 1987N2; Column length: 30. m; Column diameter: 0.25 mm
CapillaryPEG-20M140.2133.Buryan, Macák, et al., 1987N2; Column length: 30. m; Column diameter: 0.25 mm
CapillaryPEG-20M160.2159.Buryan, Macák, et al., 1987N2; Column length: 30. m; Column diameter: 0.25 mm

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.

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]

Ardashev, 1960
Ardashev, B.I., Catalytic conversion of acylated arylamines into quinolines. in Khim., Tekhnol. Primen. Proizvodnykh Piridina Khinolina, Mater. Soveshch., 1957, Inst. Khim. Akad. Nauk Latv. SSR: Riga, pp 171-4, 1960. [all data]

Ardashev and Tertov, 1957
Ardashev, B.I.; Tertov, B.A., Quinoline derivatives. XIV. Synthesis of lepidine bases from acetanilide and oxo compounds., Zh. Prikl. Khim. (Leningrad), 1957, 30, 1715. [all data]

Berlizov, Nabivach, et al., 1987
Berlizov, Yu.S.; Nabivach, V.M.; Mitrikov, V.P., Capillary gas chromatography of alkylquinolines, Zh. Anal. Khim., 1987, 62, 6, 1119-1124. [all data]

Buryan, Macák, et al., 1987
Buryan, P.; Macák, J.; Triska, J.; Vodicka, L.; Berlizov, Yu.S.; Dmitrikov, V.P.; Nabivach, V.M., Kováts retention indices of alkylquinolines on capillary columns, J. Chromatogr., 1987, 391, 89-96, https://doi.org/10.1016/S0021-9673(01)94307-9 . [all data]


Notes

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