Difference between revisions of "Erythrosine"

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== Description ==
 
== Description ==
  
A brown powder that forms a cherry red synthetic dye solution with water. First discovered in 1876 by Kussamaul, erythrosine is an iodinate derivative of [http://cameo.mfa.org/materials/fullrecord.asp?name=fluorescein fluorescein]. It is used as a direct dye on [http://cameo.mfa.org/materials/fullrecord.asp?name=wool wool] and [http://cameo.mfa.org/materials/fullrecord.asp?name=silk silk]. Erythrosine is also used in inks, lacquers, cosmetics, and as a lake pigment. It is not colorfast in [http://cameo.mfa.org/materials/fullrecord.asp?name=solar%20radiation sunlight].
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A brown powder that forms a cherry red synthetic dye solution with water. First discovered in 1876 by Kussamaul, erythrosine is an iodinate derivative of [[fluorescein]]. It is used as a direct dye on [[wool]] and [[silk]]. Erythrosine is also used in inks, lacquers, cosmetics, and as a lake pigment. It is not colorfast in [[solar radiation|sunlight]].
  
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[[[SliderGallery rightalign|erythrosine.jpg~Chemical structure]]]
 
== Synonyms and Related Terms ==
 
== Synonyms and Related Terms ==
  
 
erythrosine B; erythrosine BS; Acid Red 51; CI 45430; FD&C Red No.3; Food Red 14; Pigment Red 172 (aluminum salt); Solvent Red 140; érythrosine (Fr.); eritrosina (Esp., Port.); sodium iodeosin; erythrosin
 
erythrosine B; erythrosine BS; Acid Red 51; CI 45430; FD&C Red No.3; Food Red 14; Pigment Red 172 (aluminum salt); Solvent Red 140; érythrosine (Fr.); eritrosina (Esp., Port.); sodium iodeosin; erythrosin
  
[[[SliderGallery rightalign|erythrosine.jpg~Chemical structure]]]
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== Risks ==
 
 
== Other Properties ==
 
  
Soluble in water, ethanolAn aqueous solution of erythrosine will form a yellow-brown precipitate when drops of HCl are added and a red precipitate when drops of NaOH solution are added.
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* Toxicity and carcinogenicity are being studied.   
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* MilliporeSigma: [https://www.emdmillipore.com/US/en/product/msds/MDA_CHEM-115936?ReferrerURL=https%3A%2F%2Fsearch.yahoo.com%2F&bd=1 SDS]
  
Maximum absorption wavelength = 524 nm. 
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==Physical and Chemical Properties==
  
The fluorescence of erythrosine changes with pH.  It is colorless at pH 4.0 changing to a fluorescescent yellow-green at pH 4.5
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* Soluble in water, ethanol. 
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* An aqueous solution of erythrosine will form a yellow-brown precipitate when drops of HCl are added and a red precipitate when drops of NaOH solution are added. 
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* Maximum absorption wavelength = 524 nm. 
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* The fluorescence of erythrosine changes with pH.  It is colorless at pH 4.0 changing to a fluorescent yellow-green at pH 4.5
  
 
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== Hazards and Safety ==
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==Resources and Citations==
 
 
Toxicity and carcinogenicity are being studied. 
 
 
 
Mallinckrodt Baker: [http://www.jtbaker.com/msds/englishhtml/e1675.htm MSDS]
 
 
 
== Additional Information ==
 
 
 
M.Ballard (ed.), ''Important Early Synthetic Dyes. Chemistry, Constitution, Date, Properties.'' Conservation Analytical Laboratory, Smithsonian Institution, 1991.
 
  
== Authority ==
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* M.Ballard (ed.), ''Important Early Synthetic Dyes. Chemistry, Constitution, Date, Properties.'' Conservation Analytical Laboratory, Smithsonian Institution, 1991.
  
 
* Richard S. Lewis, ''Hawley's Condensed Chemical Dictionary'', Van Nostrand Reinhold, New York, 10th ed., 1993
 
* Richard S. Lewis, ''Hawley's Condensed Chemical Dictionary'', Van Nostrand Reinhold, New York, 10th ed., 1993
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* ''The Merck Index'', Martha Windholz (ed.), Merck Research Labs, Rahway NJ, 10th edition, 1983  Comment: entry 3734
 
* ''The Merck Index'', Martha Windholz (ed.), Merck Research Labs, Rahway NJ, 10th edition, 1983  Comment: entry 3734
  
* External source or communication  Comment: T.Schafer, C. Norton, V.Blyth-Hill, "The Efficacy of Using Boards Containing Zeolites in Passepartout for Works of Art on Paper, WAAC Newsletter, 22(1):14, 2000. -erythrosine fades rapidly
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* T.Schafer, C. Norton, V.Blyth-Hill, "The Efficacy of Using Boards Containing Zeolites in Passepartout for Works of Art on Paper, WAAC Newsletter, 22(1):14, 2000. -erythrosine fades rapidly
  
 
* Colour Index International online at www.colour-index.org  Comment: discoverer = Kussmaul; CAS=16423-68-0, 12227-78-0, 15905-32-5
 
* Colour Index International online at www.colour-index.org  Comment: discoverer = Kussmaul; CAS=16423-68-0, 12227-78-0, 15905-32-5

Latest revision as of 13:16, 5 August 2022

Description

A brown powder that forms a cherry red synthetic dye solution with water. First discovered in 1876 by Kussamaul, erythrosine is an iodinate derivative of Fluorescein. It is used as a direct dye on Wool and Silk. Erythrosine is also used in inks, lacquers, cosmetics, and as a lake pigment. It is not colorfast in sunlight.

Chemical structure

Erythrosine.jpg

Synonyms and Related Terms

erythrosine B; erythrosine BS; Acid Red 51; CI 45430; FD&C Red No.3; Food Red 14; Pigment Red 172 (aluminum salt); Solvent Red 140; érythrosine (Fr.); eritrosina (Esp., Port.); sodium iodeosin; erythrosin

Risks

  • Toxicity and carcinogenicity are being studied.
  • MilliporeSigma: SDS

Physical and Chemical Properties

  • Soluble in water, ethanol.
  • An aqueous solution of erythrosine will form a yellow-brown precipitate when drops of HCl are added and a red precipitate when drops of NaOH solution are added.
  • Maximum absorption wavelength = 524 nm.
  • The fluorescence of erythrosine changes with pH. It is colorless at pH 4.0 changing to a fluorescent yellow-green at pH 4.5
Composition C20H6I4Na2O5
CAS 16423-68-0
Molecular Weight mol. wt. = 879.86

Resources and Citations

  • M.Ballard (ed.), Important Early Synthetic Dyes. Chemistry, Constitution, Date, Properties. Conservation Analytical Laboratory, Smithsonian Institution, 1991.
  • Richard S. Lewis, Hawley's Condensed Chemical Dictionary, Van Nostrand Reinhold, New York, 10th ed., 1993
  • The Merck Index, Martha Windholz (ed.), Merck Research Labs, Rahway NJ, 10th edition, 1983 Comment: entry 3734
  • T.Schafer, C. Norton, V.Blyth-Hill, "The Efficacy of Using Boards Containing Zeolites in Passepartout for Works of Art on Paper, WAAC Newsletter, 22(1):14, 2000. -erythrosine fades rapidly
  • Colour Index International online at www.colour-index.org Comment: discoverer = Kussmaul; CAS=16423-68-0, 12227-78-0, 15905-32-5
  • CRC Handbook of Chemistry and Physics, Robert Weast (ed.), CRC Press, Boca Raton, Florida, v. 61, 1980 Comment: The fluorescence of erythrosine changes with pH. It is colorless at pH 4.0 changing to a fluorescescent yellow-green at pH 4.5
  • Sigma Dyes, Stains and Natural Pigments, Infrared Library, Nicolet, 1991-1995 Comment: OMNIC for Erythrosine B: formula= C20H8I4O5, CAS= 15905-32-5 and for sodium salt of Erythrosine B: formula=C20H6I4Na2O5, CAS= 568-63-8