542
Views
1
CrossRef citations to date
0
Altmetric
Original Articles

Quirks of dye nomenclature. 10. Eosin Y and its close relatives

ORCID Icon

References

  • Agarwal A, Gupta S, Sharma R (2016) Eosin-nigrosin staining procedure. In: Agarwal A, Gupta S, Sharma R, Eds. Andrological Evaluation of Male Infertility. Springer, Heidelberg. pp. 73–77.
  • Aldrich (2009) Handbook of Fine Chemicals. Aldrich, Milwaukee, WI. p. 1247.
  • Anonymous (1921) Gustav Mann. An obituary. Brit. Med. J. Sept. 17(1921): 465.
  • Anselmi C, Capitani D, Tintaru A, Doherty B, Sgamellotti A, Miliani C (2017) Beyond the color: a structural insight to eosin-based lakes. Dyes Pigments 140: 297–311.
  • Arnold L (1927) Gustav Mann, 1864–1921. Stain Technol. 2: 4–7.
  • Assefi P, Ghaedi M, Ansari A, Habibi MH, Momeni MS (2014) Artificial neural network optimization for removal of hazardous dye eosin Y from aqueous solution using Co2O3-NP-AC: isotherm and kinetics study. J. Ind. Eng. Chem. 20: 2905–2913.
  • Assi R, Foster TR, He H, Stamati K, Bai H, Huang Y, Hyder F, Douglas D, Shu C, Homer-Vanniasinkam S, Cheema U, Dardik A (2016) Delivery of mesenchymal stem cells in biomimetic engineered scaffolds promotes healing of diabetic ulcers. Regen. Med. 11: 245–260.
  • Baeyer A (1875) Zur Geschichte des Eosins. Ber. Dtsch. Chem. Ges. 8: 146–148.
  • Baeyer A (1876) Ueber die Verbindungen der Phtalsäure mit den Phenolen. Ann. Chem. 183: 1–74.
  • Barcia JJ (2007) The Giemsa stain: its history and applications. Int. J. Surg. Pathol. 15: 292–296.
  • Brekland (2016) Brekland Scientific safety data sheet for eosin, product code 0001126. Breckland Scientific, Stafford.
  • Centeno SA, Hale C, Carò F, Cesaratto A, Shibayama N, Delaney J, Dooley K, van der Snickt G, Janssens K, Stein SA (2017) Van Gogh’s Irises and Roses: the contribution of chemical analyses. Herit. Sci. 5: 18.
  • Chatterjee S, Chatterjee S, Chatterjee BP, Das AR, Guha AK (2005) Adsorption of a model anionic dye, eosin Y, from aqueous solution by chitosan hydrobeads. J. Coll. Interf. Sci. 288: 30–35.
  • Chowdhury AP, Shambharkar BH, Ghugal SG, Umare SS, Shende AG (2016) Ethylene glycol mediated synthesis of SnS quantum dots and their application towards degradation of eosin yellow and brilliant green dyes under solar irradiation. RSC Adv. 6: 108290–108297.
  • Claro A, Melo MJ, de Melo JSS, van den Berg KJ, Burnstock A, Montague M, Newman R (2010) Identification of red colorants in van Gogh paintings and ancient Andean textiles by microspectrofluorimetry. J. Cult. Herit. 11: 27–34.
  • Conn HJ (1925) Biological Stains, a Handbook on the Nature and Uses of the Dyes Employed in the Biological Laboratory. Commission on Standardization of Biological Stains, Geneva, NY. pp. 80, 97.
  • Conn HJ (1953) Biological Stains, a Handbook on the Nature and Uses of the Dyes Employed in the Biological Laboratory. 6th ed., Williams & Wilkins, Baltimore. pp. 189, 327–328.
  • Cook HC (1997) Origins of tinctorial methods in histology. J. Clin. Pathol. 50: 716–720.
  • Cooksey CJ (2017a) Quirks of dye nomenclature. 8. Methylene blue, azure and violet. Biotech. & Histochem. 92: 347–356.
  • Cooksey CJ (2017b) Quirks of dye nomenclature. 9. Fluorescein. Biotech. & Histochem. 1–7. Published online Sept 14, 2017.
  • Crace-Calvert F (1878) Dyeing and Calico Printing. Simpkin, Marshall, & Co., London. p. 252.
  • de Keijzer M, van Bommel MR (2017) Bright new colours: the history and analysis of fluorescein, eosine, erythrosine, rhodamine and some of their derivatives. In: Kirby J, Ed. The Diversity of Dyes in History and Archaeology. Archetype Publ., London. pp. 326–338.
  • Degano I, Tognotti P, Kunzelman D, Modugno F (2017) HPLC-DAD and HPLC-ESI-Q-ToF characterisation of early 20th century lake and organic pigments from Lefranc archives. Herit. Sci. 5: 7.
  • Dronsfield A, Edmonds J (2001) The Transition from Natural to Synthetic Dyes 1856–1920. Self Published, Little Chalfont.
  • Eastaugh N, Walsh V, Chaplin T, Siddall R (2013) Pigment Compendium: Dictionary and Optical Microscopy of Historical Pigments. Routledge, Oxford. p. 157.
  • Emery AJ, Stotz E (1952) Paper chromatography for analysis of a dye mixture. Stain Technol. 27: 21–28.
  • Estevão BM, Pellosi DS, de Freitas CF, Vanzin D, Franciscato DS, Caetano W, Hioka N (2014) Interaction of eosin and its ester derivatives with aqueous biomimetic micelles: evaluation of photodynamic potentialities. J. Photochem. Photobiol. A: Chem. 287: 30–39.
  • Feng C, Zheng LP, Yan GY, Zheng MQ (2011) Photocatalytic degradation of eosin B by ZnS nanoparticles under visible light. Adv. Mat. Res. 236–238: 2080–2085.
  • Fieberg JE, Knutås P, Hostettler K, Smith GD (2017) “Paintings fade like flowers”: pigment analysis and digital reconstruction of a faded pink lake pigment in Vincent van Gogh’s undergrowth with two figures. Appl. Spectrosc. 71: 794–808.
  • Fischer E (1876) Eosin als Tinctionsmittel für mikroskopische Präparate. Arch. Mikrosk. Anat. 12: 349–352.
  • Galigher AE (1934) The Essentials of Practical Microtechnique in Animal Biology. Albert E. Galigher, Berkeley, CA.
  • Green AG (1904) A Systematic Survey of the Organic Colouring Matters. Macmillan, London. p. 209.
  • Gyawali P, Sidhu JPS, Ahmed W, Jagals P, Toze S (2016) An approach to reduce false viability assessment of hookworm eggs with vital stains. Food Waterborne Parasitol. 3: 9–12.
  • Hari DP, König B (2014) Synthetic applications of eosin Y in photoredox catalysis. Chem. Comm. 50: 6688–6699.
  • Harrison WT, Ramadevi P, Seethalakshmi PG, Kumaresan S (2007) 4-Aza-1-azoniabicyclo [2.2.2] octane eosinide. Acta Cryst. E 63: o3911–o3911.
  • Harrow B (1920) Eminent Chemists of Our Time. D. van Nostrand, New York. pp. 217–239.
  • Hewitt JT, Woodforde AWG (1902) Bromonitro-derivatives of fluorescein. J. Chem. Soc. Trans. 81: 893–900.
  • Hofmann AW (1875) Ueber das Eosin. Ber. Dtsch. Chem. Ges. 8: 62–66.
  • Holmes WC, Melin CG, Peterson AR (1932) Eosin B. Stain Technol. 7: 121–127.
  • Huang B, Zhao Y, Yang C, Gao Y, Xia W (2017) Combining eosin Y with Selectfluor: a regioselective brominating system for para-bromination of aniline derivatives. Org. Lett. 19: 3799–3802.
  • Kay AB (2015) The early history of the eosinophil. Clin. Exp. Aller. 45: 575–582.
  • Koch P, Bahmer FA, Hausen BM (1995) Allergic contact dermatitis from purified eosin. Contact Derm. 32: 92–95.
  • Kola L (2010) Physical and chemical parameters impact on eosin spectral determinations. Maced. J. Chem. Chem. Eng. 29: 51–56.
  • Krafts KP, Hempelmann E, Oleksyn BJ (2011) The color purple: from royalty to laboratory, with apologies to Malachowski. Biotech. & Histochem. 86: 7–35.
  • Lee RE, Young RH, Castleman B (2002) James Homer Wright: a biography of the enigmatic creator of the Wright stain on the occasion of its centennial. Am. J. Surg. Pathol. 26: 88–96.
  • Lillie RD (1941) Romanowsky staining with buffered solutions. III. Extension of the method to Romanowsky stains in general. Stain Technol. 16: 1–6.
  • Mann G (1902) Physiological Histology, Methods and Theory. Clarendon Press, Oxford.
  • Marshall PN, Lewis SM (1974) A rapid thin-layer chromatographic system for Romanowsky blood stains. Stain Technol. 49: 235–240.
  • Mchedlov-Petrossyan NO, Kleshchevnikova VN (1994) Influence of the cetyltrimethylammonium chloride micellar pseudophase on the protolytic equilibria of oxyxanthene dyes at high bulk phase ionic strength. J. Chem. Soc. Farad. Trans. 90: 629–640.
  • Michener CD, Cross EA, Daly HV, Rettenmeyer CW, Wille A (1955) Additional techniques for studying the behavior of wild bees. Insect. Soc. 2: 237–246.
  • Mittal A, Jhare D, Mittal J (2013) Adsorption of hazardous dye eosin yellow from aqueous solution onto waste material de-oiled soya: isotherm, kinetics and bulk removal. J. Mol. Liq. 179: 133–140.
  • Mittal J, Jhare D, Vardhan H, Mittal A (2014) Utilization of bottom ash as a low-cost sorbent for the removal and recovery of a toxic halogen containing dye eosin yellow. Desalin. Water Treat. 52: 4508–4519.
  • Montroni D, Piccinetti C, Fermani S, Calvaresi M, Harrington MJ, Falini G (2017) Exploitation of mussel byssus mariculture waste as a water remediation material. RSC Adv. 7: 36605–36611.
  • Neckers DC (1987) The Indian happiness wart in the development of photodynamic action. J. Chem. Educ. 64: 649–656.
  • Oba Y, Poulson SR (2012) Octanol-water partition coefficients (Kow) vs. pH for fluorescent dye tracers (fluorescein, eosin Y), and implications for hydrologic tracer tests. Geochem. J. 46: 517–520.
  • Orndorff WR, Hemmer AJ (1927) Fluorescein and some of its derivatives. J. Am. Chem. Soc. 49: 1272–1280.
  • Otterstätter G (1999) Coloring of Food, Drugs, and Cosmetics. Marcel Dekker, New York. p. 230.
  • Perkin WH (1885) The colouring matters produced from coal-tar. J. Soc. Chem. Ind. 4: 426–456.
  • Ploskonos MB (2014) The application of eosin and propidium iodide in evaluation of vitality of human spermatozoa. Klin. Lab. Diagn. 59: 22–25. [Russian].
  • Reinhardt C, Travis AS (2000) Heinrich Caro and the Creation of Modern Chemical Industry. Kluwer Academic, London. p. 8.
  • Sinha T, Ahmaruzzaman M (2015) A novel green and template free approach for the synthesis of gold nanorice and its utilization as a catalyst for the degradation of hazardous dye. Spectrochim. Acta A 142: 266–270.
  • Srivastava V, Singh PP (2017) Eosin Y catalysed photoredox synthesis: a review. RSC Adv. 7: 31377–31392.
  • Sudborough JJ, James TC (1931) Practical Organic Chemistry. Blackie & Son, London and Glasgow. p. 285.
  • TCI (2014) TCI America safety data sheet for acid red 87, catalog T0037. TCI America, Portland, OR.
  • Tomb RR (1991) Allergic contact dermatitis from eosin. Contact Derm. 24: 27–29.
  • Van Liedekerke BM, Nelis HJ, Wittekind DH, De Leenheer AP (1991) Stability study of azure B, eosin Y and commercial Romanowsky Giemsa stock solutions using high performance liquid chromatography. Histochem. J. 23: 189–195.
  • Vanzin D, Freitas CF, Pellosi DS, Batistela VR, Machado AEH, Pontes RM, Caetano W, Hioka N (2016) Experimental and computational studies of protolytic and tautomeric equilibria of erythrosin B and eosin Y in water/DMSO. RSC Adv. 6: 110312–110328.
  • Wang Y, Yu Z, Zhang J, Moussian B (2016) Regionalization of surface lipids in insects. Proc. R. Soc. B 283: 20152994 (8 pages).
  • Wegener JW, Klamer JC, Govers H, Brinkman UT (1987) Determination of organic colorants in cosmetic products by high-performance liquid chromatography. Chromatographia 24: 865–875.
  • Weyl T (1892) The Coal-Tar Colors. Blakiston, Philadelphia. p. 26.
  • Wright JH (1902) A rapid method for the differential staining of blood films and malarial parasites. J. Med. Res. 7: 138–144.
  • Yang X-J, Chen B, Zheng L-Q, Wu L-Z, Tung C-H (2014) Highly efficient and selective photocatalytic hydrogenation of functionalized nitrobenzenes. Green Chem. 16: 1082–1086.
  • Zha SW, Lu NQ, Xhu HQ (2015) Eosin Y-water test for sperm function examination. Zhonghua Nan Ke Xue [Nat. J. Androl.] 21: 566–569. [Chinese].
  • Zhang R, Yu Z, Yao Y, Hou X, Shen Q, Wang L, Guo X, Wang J, Zhu X (2017b) Selective adsorption and separation of organic dyes with spherical polyelectrolyte brushes and compressed carbon dioxide. Chem. Eur. J. 23: 13696–13703.
  • Zhang Y, Ye C, Li S, Ding A, Gu G, Guo H (2017a) Eosin Y-catalyzed photooxidation of triarylphosphines under visible light irradiation and aerobic conditions. RSC Adv. 7: 13240–13243.
  • Zinatloo-Ajabshir S, Mortazavi-Derazkola S, Salavati-Niasari M (2017) Sonochemical synthesis, characterization and photodegradation of organic pollutant over Nd2O3 nanostructures prepared via a new simple route. Sep. Purif. Technol. 178: 138–146.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.