Disperse Yellow 1

• Formula: C₁₂H₉N₃O₅
• Molecular weight: 275.2170
• IUPAC Standard InChI: InChI=1S/C12H9N3O5/c16-10-4-1-8(2-5-10)13-11-6-3-9(14(17)18)7-12(11)15(19)20/h1-7,13,16H Copy

  
• IUPAC Standard InChIKey: BCPQALWAROJVLE-UHFFFAOYSA-N Copy
• CAS Registry Number: 119-15-3
• 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: Phenol, 4-[(2,4-dinitrophenyl)amino]-; Phenol, p-(2,4-dinitroanilino)-; Acetamine Yellow 2R; Acetoquinone Light Yellow 2RZ; Amacel Yellow RR; C.I. Disperse Yellow 1; C.I. 10345; Celliton Fast Yellow RR; Celliton Fast Yellow RRA-CF; Cilla Fast Yellow RR; Disperse Fast Yellow 2K; Disperse Yellow R; Dispersol Fast Yellow A; Dispersol Printing Yellow A; Fast Disperse Yellow 2K; Fenacet Fast Yellow 2R; Kayalon Fast Yellow RR; Microsetile Yellow 2R; N-2,4-Dinitrophenyl-4-aminophenol; Nyloquinone Yellow 2R; Perliton Yellow RR; Reliton Yellow R; Serisol Fast Yellow A; Setacyl Yellow P-BS; Supracet Fast Yellow 2R; Supracet Yellow RR; SRA Golden Yellow VIII; 2,4-Dinitro-4'-hydroxydiphenylamine; 4-(2,4-Dinitroanilino)phenol; 4-[(2,4-Dinitrophenyl)amino]phenol; 4-Hydroxy-2',4'-dinitrodiphenylamine; 4'-Hydroxy-2,4-dinitrodiphenylamine; p-(2,4-Dinitroanilino)phenol; Permanent Yellow 2K; C.I. Solvent Yellow 52; 2,4-Dinitro-p-hydroxydiphenylamine; Dispersol yellow B-A; Disperse yellow stable 2K; Synten yellow P 2R; N-(2,4-Dinitrophenyl)-N-(4-hydroxyphenyl)amine; NSC 13965
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• Information on this page:
  • Phase change data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • UV/Visible spectrum
  • References
  • Notes
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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

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

Mass spectrum (electron ionization)

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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

Spectrum

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Additional Data

UV/Visible 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: Victor Talrose, Alexander N. Yermakov, Alexy A. Usov, Antonina A. Goncharova, Axlexander N. Leskin, Natalia A. Messineva, Natalia V. Trusova, Margarita V. Efimkina

Spectrum

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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.

Kojima, 1970
Kojima, H., Sen'i Gakkaishi, 1970, 26, 530. [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]

Lang (editor), 1967
Lang (editor), L., Absorption Spectra in the Ultraviolet and Visible Region, 1967, 8, 85. [all data]

Notes

Go To: Top, Phase change data, IR Spectrum, Mass spectrum (electron ionization), UV/Visible spectrum, References

• Symbols used in this document:
  

  ΔsubH

  Enthalpy of sublimation

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