Benzenamine, 4-(phenylazo)-

• Formula: C₁₂H₁₁N₃
• Molecular weight: 197.2358
• IUPAC Standard InChI: InChI=1S/C12H11N3/c13-10-6-8-12(9-7-10)15-14-11-4-2-1-3-5-11/h1-9H,13H2 Copy

  
• IUPAC Standard InChIKey: QPQKUYVSJWQSDY-UHFFFAOYSA-N Copy
• CAS Registry Number: 60-09-3
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
  The 3d structure may be viewed using Java or Javascript.
• Stereoisomers:
  • Benzenamine,4-(phenylazo)-(E)-
• Other names: C.I. Solvent Yellow 1; p-(Phenylazo)aniline; p-Aminoazobenzene; p-Aminoazobenzol; p-Aminodiphenyldiimide; Aniline Yellow; Brasilazina Oil Yellow G; C.I. 11000; Cellitazol R; Ceres Yellow R; Fast Spirit Yellow; Fat Yellow AAB; Induline R; Oil Soluble Aniline Yellow; Oil Yellow AAB; Oil Yellow AB; Oil Yellow AN; Oil Yellow B; Organol Yellow 2A; Solvent Yellow 1; Somalia Yellow 2G; Sudan Yellow R; 4-Aminoazobenzene; 4-Aminoazobenzol; 4-Phenylazoaniline; p-(Phenolazo)aniline; p-(Phenylazo)phenylamine; p-Amimoazobenzene; Aminoazobenzene; Aniline, p-(phenylazo)-; Azobenzene, 4-amino-; C.I. Solvent Blue 7; Fast Spirit Yellow AAB; Oil Yellow R; Oil Yellow 2G; Oil-Sol. Aniline Yellow; Organol Yellow; Stearix Brown 4R; Sudan Yellow RA; USAF EK-1375; 4-(Phenylazo)benzenamine; 4-Amino-1,1'-azobenzene; 4-Benzeneazoaniline; Paraphenolazo aniline; Zlut anilinova; Zlut rozpoustedlova 1; Benzenamine, 4-(2-phenyldiazenyl)-; p-Aminodiphenylimide
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• Information on this page:
  • Phase change data
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • UV/Visible spectrum
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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
AC - William E. Acree, Jr., James S. Chickos

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.

Buckingham and Donaghy, 1982
Buckingham, J.; Donaghy, S.M., Dictionary of Organic Compounds: Fifth Edition, Chapman and Hall, New York, 1982, 1. [all data]

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

Majury, 1956
Majury, T.G., Chem. Ind., 1956, 17, 349. [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]

Baughman and Perenich, 1988, 2
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

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

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