8-Hydroxyquinoline

• Formula: C₉H₇NO
• Molecular weight: 145.1580
• IUPAC Standard InChI: InChI=1S/C9H7NO/c11-8-5-1-3-7-4-2-6-10-9(7)8/h1-6,11H Copy

  
• IUPAC Standard InChIKey: MCJGNVYPOGVAJF-UHFFFAOYSA-N Copy
• CAS Registry Number: 148-24-3
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Other names: Oxyquinoline; 8-Quinolinol; Bioquin; Oxin; Oxine; Oxychinolin; Phenopyridine; Quinophenol; Tumex; 1-Azanaphthalene-8-ol; 8-Hydroxychinolin; 8-Oxyquinoline; 8-OQ; 8-Quinol; Hydroxybenzopyridine; Oxybenzopyridine; Oxychinoline; 8-Oxyquinolin; Fennosan H 30; NCI-C55298; USAF EK-794; 8-Chinolinol; Fennosan; o-Oxychinolin; 8-Quinolol; Oxoquinoline; Quinolin-8-ol; NSC 2039; NSC 615011; NSC 82404
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• Information on this page:
  • Phase change data
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • UV/Visible spectrum
  • Gas Chromatography
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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
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
AC - William E. Acree, Jr., James S. Chickos

Reduced pressure boiling point

Enthalpy of sublimation

Enthalpy of fusion

References

Go To: Top, Phase change data, Notes

Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Manske, Ledingham, et al., 1949
Manske, R.H.F.; Ledingham, A.E.; Ashford, W.R., The preparation of quinolins by a modified Skraup reaction., Can. J. Res., 1949, 27F, 359. [all data]

Aldrich Chemical Company Inc., 1990
Aldrich Chemical Company Inc., Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 1. [all data]

Horton and Wendlandt, 1963
Horton, G.R.; Wendlandt, W.W., The heats of dissociation of the 8-quinolinol and substituted 8-quinolinol metal chelates of uranium (VI), thorium (IV) and scandium (III), J. Inorg. Nucl. Chem., 1963, 25, 241-245. [all data]

Cox and Pilcher, 1970
Cox, J.D.; Pilcher, G., Thermochemistry of Organic and Organometallic Compounds, Academic Press Inc., London, 1970, 643. [all data]

Stephenson and Malanowski, 1987
Stephenson, Richard M.; Malanowski, Stanislaw, Handbook of the Thermodynamics of Organic Compounds, 1987, https://doi.org/10.1007/978-94-009-3173-2 . [all data]

WANG, TAN, et al., 2008
WANG, Shao-Xu; TAN, Zhi-Cheng; LI, Yan-Sheng; TONG, Bo; LI, Ying; SHI, Quan; ZHANG, Jing-Nan, Thermodynamic Study of 8-Hydroxyquinoline by Adiabatic Calorimetry and Thermal Analysis, Chin. J. Chem., 2008, 26, 11, 2016-2020, https://doi.org/10.1002/cjoc.200890360 . [all data]

Zorel, Costalonga, et al., 2001
Zorel, H.E., Jr.; Costalonga, A.G.C.; Crespi, M.S.; Ribiero, C.A., Quim. Nova, 2001, 24, 5, 599. [all data]

Notes

Go To: Top, Phase change data, References

• Symbols used in this document:
  

  Tboil	Boiling point
  Tfus	Fusion (melting) point
  ΔfusH	Enthalpy of fusion
  ΔsubH	Enthalpy of sublimation
  ΔsubH°	Enthalpy of sublimation at standard conditions

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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