9,10-Anthracenedione, 1-amino-

• Formula: C₁₄H₉NO₂
• Molecular weight: 223.2268
• IUPAC Standard InChI: InChI=1S/C14H9NO2/c15-11-7-3-6-10-12(11)14(17)9-5-2-1-4-8(9)13(10)16/h1-7H,15H2 Copy

  
• IUPAC Standard InChIKey: KHUFHLFHOQVFGB-UHFFFAOYSA-N Copy
• CAS Registry Number: 82-45-1
• Chemical structure:
  This structure is also available as a 2d Mol file
• Other names: Anthraquinone, 1-amino-; α-Aminoanthraquinone; α-Anthraquinonylamine; C.I. 37275; Diazo Fast Red AL; 1-Amino-9,10-anthraquinone; 1-Aminoanthraquinone; 1-Aminoanthrachinon; 1-Amino-9,10-anthracenedione; Smoke Orange G; 9,10-Dioxo-9,10-dihydro-1-anthraceneamine; NSC 30415; NSC 458
• Permanent link for this species. Use this link for bookmarking this species for future reference.
• Information on this page:
  • Phase change data
  • IR Spectrum
  • References
  • Notes
• Other data available:
  • 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 by: William E. Acree, Jr., James S. Chickos

Enthalpy of sublimation

Enthalpy of fusion

IR Spectrum

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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: Coblentz Society, Inc.

Condensed Phase Spectrum

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Notice: Except where noted, spectra from this collection were measured on dispersive instruments, often in carefully selected solvents, and hence may differ in detail from measurements on FTIR instruments or in other chemical environments. More information on the manner in which spectra in this collection were collected can be found here.

Notice: Concentration information is not available for this spectrum and, therefore, molar absorptivity values cannot be derived.

Additional Data

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.

NISHIDA, ISHIHARA, et al., 2008
NISHIDA, K.; ISHIHARA, E.; OSAKA, T.; KOUKITU, M., Vapour Pressures and Heats of Sublimation of Some Disperse Dyes, J Food Science, 2008, 93, 2, 52-54, https://doi.org/10.1111/j.1478-4408.1977.tb03324.x . [all data]

Nishida, Ishihara, et al., 1978
Nishida, K.; Ishihara, E.; Osaka, T.; Koukitu, M., Vapor pressures and heats of sublimation of some disperse dyes, Galaxia, 1978, 72, 13. [all data]

Beynon and Nicholson, 2002
Beynon, J.H.; Nicholson, G.R., A radioactive ionization gauge and its application to the measurement of latent heat of vaporization, J. Sci. Instrum., 2002, 33, 10, 376-380, https://doi.org/10.1088/0950-7671/33/10/302 . [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]

Krien, 1984
Krien, G., Thermoanalytische untersuchungen an rauchfarbstoffen, Thermochimica Acta, 1984, 81, 29-43, https://doi.org/10.1016/0040-6031(84)85108-4 . [all data]

Baughman and Perenich, 1988
Baughman, George L.; Perenich, Theresa A., Fate of dyes in aquatic systems: I. Solubility and partitioning of some hydrophobic dyes and related compounds, Environ Toxicol Chem, 1988, 7, 3, 183-199, https://doi.org/10.1002/etc.5620070302 . [all data]

Notes

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• Symbols used in this document:
  

  ΔfusH	Enthalpy of fusion
  ΔsubH	Enthalpy of sublimation

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