Difference between revisions of "Disazo dye"
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disazo pigment; diarylide; dis-azo; benzimidazolone dye | disazo pigment; diarylide; dis-azo; benzimidazolone dye | ||
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* B. Berrie, S.Q. Lomax, 'Azo Pigments: Their History, Synthesis, Properties and Use in Artists' Materials', ''Studies in the History of Art'' , National Gallery of Art, Washington DC, No. 57, 1997 | * B. Berrie, S.Q. Lomax, 'Azo Pigments: Their History, Synthesis, Properties and Use in Artists' Materials', ''Studies in the History of Art'' , National Gallery of Art, Washington DC, No. 57, 1997 | ||
| − | * Website | + | * Website: www.handprint.com |
[[Category:Materials database]] | [[Category:Materials database]] | ||
Latest revision as of 08:59, 30 October 2020
Description
A class of synthetic organic pigments formed by two coupled arylide molecules. Disazo condensation pigments were first developed in Europe in the mid 1950s and were introduced in the U.S. in 1960. Their colors range includes yellow, orange, brown, red and violet. Disazo colors, in general, have low solubility in organic solvents and fair to good lightfastness. They are used for printing inks, plastics, and paints.
Synonyms and Related Terms
disazo pigment; diarylide; dis-azo; benzimidazolone dye
Resources and Citations
- B. Berrie, S.Q. Lomax, 'Azo Pigments: Their History, Synthesis, Properties and Use in Artists' Materials', Studies in the History of Art , National Gallery of Art, Washington DC, No. 57, 1997
- Website: www.handprint.com