Home Dioxazine pigments
Article
Licensed
Unlicensed Requires Authentication

Dioxazine pigments

  • Robert Christie EMAIL logo and Adrian Abel
Published/Copyright: June 29, 2021
Become an author with De Gruyter Brill

Abstract

This chapter provides an overview of the structural and synthetic chemistry, and the industrial applications, of dioxazine pigments, a small group of high performance organic pigments. The color violet (or purple) has frequently assumed a prominent position in history, on account of its rarity and cost. The natural colorant Tyrian purple and the first synthetic textile dye, Mauveine, are prime examples of this unique historical feature. CI Pigment Violet 23, also referred to as Dioxazine Violet or Carbazole Violet, is one of the most universally used organic pigments, by far the most important industrial pigment in the violet shade area. Dioxazine Violet is also unique as the dominant industrial violet pigment providing a brilliant, intense violet color and an excellent all-round set of fastness properties. The pigment has a polycyclic molecular structure, originally described wrongly as a linear arrangement, and later shown to adopt an S-shaped arrangement on the basis of X-ray structural analysis. Two other dioxazine pigments are of rather lesser importance. The synthesis and manufacturing route to CI Pigment Violet 23 is described in the review. Finally, a survey of the principal current applications of the individual dioxazine pigments is presented.

References

1. Christie RM. Color chemistry. 2nd ed. London: RSC, Ch 9 2015.Search in Google Scholar

2. Hunger K, Schmidt MU. Industrial organic pigments. 4th ed. Weinheim: Wiley-VCH Verlag GmbH, Ch 3 2019.Search in Google Scholar

3. Chamberlain TR, In Faulkner EB, Schwartz RJ. High performance pigments. 2nd ed. Weinheim: Wiley-VCH Verlag GmbH, 2009 Ch 12.Search in Google Scholar

4. https://www.etymonline.com/word/phoenician.Search in Google Scholar

5. https://www.bbc.com/culture/article/20180801-tyrian-purple-the-regal-color-taken-from-mollusc-mucus.Search in Google Scholar

6. Cooksey CJ. Tyrian purple: 6,6ʹ-Dibromoindigo and related compounds. Molecules. 2001;6:736–69.10.3390/60900736Search in Google Scholar

7. https://www.bibliacatolica.com.br/new-jerusalem-bible/acts/16/ (Verse 14).Search in Google Scholar

8. https://color-index.com/fingerprint/view/4528.Search in Google Scholar

9. Sakaguchi I, Hayashi Y. US 4,317,908. 7 Mar 1982.Search in Google Scholar

10. Hunger K. The effect of crystal structure on color application properties of organic pigments. Rev Prog Color. 1999;29:71–84.10.1111/j.1478-4408.1999.tb00129.xSearch in Google Scholar

11. Spietschka E, Urban M, Paulus E. DE 2,742,575. (filed 5th July 2007 but withdrawn).Search in Google Scholar

12. Sanders JD. Pigments for inkmakers. London: SITA Technology, 1989:141–9.Search in Google Scholar

13. Struve WS. US 2,843,498. 15 Jul 1958.10.5694/j.1326-5377.1958.tb36588.xSearch in Google Scholar

14. Wooden G, Wallquist O. US 5,271,759. 21 Dec 1993.10.1177/009182969302100234Search in Google Scholar

15. https://www.basf.com/us/documents/en/general-business-topics/pigments/industries/plastics/Colors-and-Effects_PSG-Pigment-preparations-Polyolefins.pdf.Search in Google Scholar

16. Wilker G, Kempter PW. What’s blue stays blue: Dioxazine blue - a new, solvent-resistant pigment. Eur Coat J. 2002.Search in Google Scholar

Published Online: 2021-06-29

© 2020 Walter de Gruyter GmbH, Berlin/Boston

Downloaded on 2.10.2025 from https://www.degruyterbrill.com/document/doi/10.1515/psr-2020-0168/html?lang=en&srsltid=AfmBOoq6wDjaUUHHCooLr7Qny-LF1Q-TOUS6QGBtBwSo9P615TvbSZ0U
Scroll to top button