Difference between revisions of "Toluidine red"

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m (Text replace - "== Authority ==" to "== Sources Checked for Data in Record ==")
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[[[SliderGallery rightalign|PR003 toluidine red.jpg~FTIR|toluidine red.jpg~Chemical structure]]]
 
[[[SliderGallery rightalign|PR003 toluidine red.jpg~FTIR|toluidine red.jpg~Chemical structure]]]
  
== Other Properties ==
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== Physical and Chemical Properties ==
  
 
Soluble in many organic solvents. Insoluble in water   
 
Soluble in many organic solvents. Insoluble in water   
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== Hazards and Safety ==
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== Risks ==
  
 
Ingestion can cause cyanosis. Suspected carcinogen.   
 
Ingestion can cause cyanosis. Suspected carcinogen.   
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Fisher Scientific: [https://fscimage.fishersci.com/msds/46042.htm MSDS]
 
Fisher Scientific: [https://fscimage.fishersci.com/msds/46042.htm MSDS]
  
== Additional Information ==
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== Resources and Citations ==
 
 
° B.Berrie, S.Q.Lomax, "Azo Pigments: Their History, Synthesis, Properties and Use in Artists' Materials" in ''Studies in the History of Art'', No.57, National Gallery of Art, Washington DC, 1997.
 
 
 
== Sources Checked for Data in Record ==
 
  
 
* F. Crace-Calvert, ''Dyeing and Calico Printing'', Palmer & Howe, London, 1876
 
* F. Crace-Calvert, ''Dyeing and Calico Printing'', Palmer & Howe, London, 1876

Revision as of 12:42, 30 October 2020

Description

A line of bright, transparent red synthetic azo-type organic pigments. Toluidine reds are based on the reaction of beta-naphthol with 2-nitro-4-toluidine. Toluidine red was first synthesized in 1904 by Lucius and Brüning in Germany. It reached its peak of popular use in the 1970s. In general, toluidine reds have fair lightfastness and weather resistance, but they have a tendency to bleed especially in oil paints. They are used in industrial coatings for air-dried and baked enamels and auto finishes. Toluidine reds are also used in wax crayons, pastels and watercolors.

Synonyms and Related Terms

toluidine toner; rosotoluidine; Pigment Red 3; CI 12120; Hansa red; rouge de toluidine (Fr.);

FTIR

PR003 toluidine red.jpg

Chemical structure

Toluidine red.jpg


Physical and Chemical Properties

Soluble in many organic solvents. Insoluble in water

Resistant to acid, alkali and soap.

Composition C17H13N3O3
CAS 2425-85-6
Molecular Weight mol. wt. = 307.3

Risks

Ingestion can cause cyanosis. Suspected carcinogen.

Fisher Scientific: MSDS

Resources and Citations

  • F. Crace-Calvert, Dyeing and Calico Printing, Palmer & Howe, London, 1876
  • 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
  • M. de Keijzer, 'A survey of red and yellow modern synthetic organic artists pigments discovered in the 20th century and used in oil colors', ICOM Preprints Lyons, France, Getty Conservation Institute, Los Angeles, p. 369, 1999
  • R. J. Gettens, G.L. Stout, Painting Materials, A Short Encyclopaedia, Dover Publications, New York, 1966
  • Ralph Mayer, A Dictionary of Art Terms and Techniques, Harper and Row Publishers, New York, 1969 (also 1945 printing)
  • Reed Kay, The Painter's Guide To Studio Methods and Materials, Prentice-Hall, Inc., Englewood Cliffs, NJ, 1983
  • Monona Rossol, The Artist's Complete Health and Safety Guide, Allworth Press, New York, 1994

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