Disperse Red 11

• Formula: C₁₅H₁₂N₂O₃
• Molecular weight: 268.2674
• IUPAC Standard InChI: InChI=1S/C15H12N2O3/c1-20-10-6-9(16)11-12(13(10)17)15(19)8-5-3-2-4-7(8)14(11)18/h2-6H,16-17H2,1H3 Copy

  
• IUPAC Standard InChIKey: TUXJTJITXCHUEL-UHFFFAOYSA-N Copy
• CAS Registry Number: 2872-48-2
• Chemical structure:
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• Other names: 9,10-Anthracenedione, 1,4-diamino-2-methoxy-; Acetate Fast Pink 3B; Amacel Cerise B; Anthraquinone, 1,4-diamino-2-methoxy-; Artisil Brilliant Rose 5BP; C.I. Disperse Red 11; C.I. Solvent Violet 26; C.I. 11/52015; C.I. 62015; Celanthrene Fast Pink 3B; Celliton Fast Pink FF3B; Celliton Fast Pink FF3BA-CF; Celliton Rose FF3B; Cibacet Brilliant Pink 4BN; Cibacete Brilliant Pink 4BN; Cilla Fast Pink FF3B; Disperse Brilliant Pink; Dispersol Red B 3B; Duranol Red X 3B; Fenacet Fast Pink 3BE; Interchem Acetate Pink 3B; Miketon Fast Pink FF 3B; Nacelan Pink 3B; Palanil Violet 6R; Perliton Red Violet FFB; Samaron Red Violet F3B; Seriplas Red X3B; Serisol Brilliant Red X 3B; Setacyl Red P-3B; Solvent Violet 26; Supracet Fast Pink 3B; Teraprint Red 6B; Terasil Brilliant Pink 4BN; 1,4-Da-2-moa; 1,4-Diamino-2-methoxyanthraquinone; 1,4-Diamino-2-methoxyanthroquinone; Cerven disperzni 11; Disperse Brilliant Rose; Violet rozpoustedlova 26; NSC 81266; 1,4-Diamino-2-methoxyanthra-9,10-quinone
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• Information on this page:
  • Phase change data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • 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 as indicated in comments:
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
AC - William E. Acree, Jr., James S. Chickos

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

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

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.

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]

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

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• Symbols used in this document:
  

  Tfus	Fusion (melting) point
  ΔfusH	Enthalpy of fusion

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