Difference between revisions of "Alizarin yellow"

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== Description ==
 
== Description ==
  
Alizarin yellow crystallizes as orange-brown needles from a dilute glacial [http://cameo.mfa.org/materials/fullrecord.asp?name=acetic acid acetic acid] solution. Developed in 1887 by R. Nietzki, it became the first azo [http://cameo.mfa.org/materials/fullrecord.asp?name=mordant dye mordant dye]. Alizarin yellow produces a dull yellow-brown, transparent pigment when precipitated on an inert base that has poorer color stability than [http://cameo.mfa.org/materials/fullrecord.asp?name=alizarin, synthetic alizarin]. The sodium salt of alizarin yellow is used as an aqueous acid-base indicator. It changes from yellow at pH 10.2 to red at pH 12.0.
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Alizarin yellow crystallizes as orange-brown needles from a dilute glacial [[acetic%20acid|acetic acid]] solution. Developed in 1887 by R. Nietzki, it became the first azo [[mordant%20dye|mordant dye]]. Alizarin yellow produces a dull yellow-brown, transparent pigment when precipitated on an inert base that has poorer color stability than [[alizarin%2C%20synthetic|alizarin]]. The sodium salt of alizarin yellow is used as an aqueous acid-base indicator. It changes from yellow at pH 10.2 to red at pH 12.0.
  
 
== Synonyms and Related Terms ==
 
== Synonyms and Related Terms ==
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[[[SliderGallery rightalign|alizarin yellow.jpg~Chemical structure]]]
 
[[[SliderGallery rightalign|alizarin yellow.jpg~Chemical structure]]]
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== Risks ==
  
== Other Properties ==
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Fisher Scientific: [https://fscimage.fishersci.com/msds/83808.htm MSDS]
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== Physical and Chemical Properties ==
  
Soluble in water and ethanol. Slightly soluble in acetone and Cellosolve. Insoluble in other organic solvents.
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Soluble in water and ethanol. Slightly soluble in acetone and Cellosolve®. Insoluble in other organic solvents.
  
 
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== Hazards and Safety ==
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== Resources and Citations ==
 
 
Fisher Scientific: [https://fscimage.fishersci.com/msds/83808.htm MSDS]
 
 
 
== Authority ==
 
  
* Ralph Mayer, Ralph Mayer, ''A Dictionary of Art Terms and Techniques'', Harper and Row Publishers, New York, 1969 (also 1945 printing)
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* Ralph Mayer, ''A Dictionary of Art Terms and Techniques'', Harper and Row Publishers, New York, 1969 (also 1945 printing)
  
* A.Scharff, A.Scharff, 'Synthetic dyestuffs for textiles and their fastness to washing', ''ICOM-CC Preprints'' Lyon, Getty Conservation Institute, Los Angeles, 1999  Comment: p.654-660
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* A.Scharff, 'Synthetic dyestuffs for textiles and their fastness to washing', ''ICOM-CC Preprints'' Lyon, Getty Conservation Institute, Los Angeles, 1999  Comment: p.654-660
  
 
* Colour Index International online at www.colour-index.org  Comment: developer, date, CAS#=584-42-9, structure verified
 
* Colour Index International online at www.colour-index.org  Comment: developer, date, CAS#=584-42-9, structure verified
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* Sigma Dyes, Stains and Natural Pigments, Infrared Library, Nicolet, 1991-1995  Comment: CAS#=2243-76-7
 
* Sigma Dyes, Stains and Natural Pigments, Infrared Library, Nicolet, 1991-1995  Comment: CAS#=2243-76-7
  
* Website address 1, Website address 1  Comment: www.straw.com/sig/dyehist
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* Website: www.straw.com/sig/dyehist
  
 
* Art and Architecture Thesaurus Online, http://www.getty.edu/research/tools/vocabulary/aat/, J. Paul Getty Trust, Los Angeles, 2000
 
* Art and Architecture Thesaurus Online, http://www.getty.edu/research/tools/vocabulary/aat/, J. Paul Getty Trust, Los Angeles, 2000

Latest revision as of 14:19, 30 October 2020

Description

Alizarin yellow crystallizes as orange-brown needles from a dilute glacial Acetic acid solution. Developed in 1887 by R. Nietzki, it became the first azo Mordant dye. Alizarin yellow produces a dull yellow-brown, transparent pigment when precipitated on an inert base that has poorer color stability than alizarin. The sodium salt of alizarin yellow is used as an aqueous acid-base indicator. It changes from yellow at pH 10.2 to red at pH 12.0.

Synonyms and Related Terms

Mordant Yellow 1; CI 14030; alizarine yellow R; p-nitrophenylazosalicylate acid; 2-hydroxy-5-[(4-nitrophenyl)azo]benzoic acid; amarilo de alizarina (Esp.); jaune d'alizarine (Fr.); giallo d'alizarina (It.); amarelo de alizarina (Port.)

Chemical structure

Alizarin yellow.jpg

Risks

Fisher Scientific: MSDS

Physical and Chemical Properties

Soluble in water and ethanol. Slightly soluble in acetone and Cellosolve®. Insoluble in other organic solvents.

Composition C13H9N3O5
CAS 584-42-9
Molecular Weight mol. wt. = 309.20

Resources and Citations

  • Ralph Mayer, A Dictionary of Art Terms and Techniques, Harper and Row Publishers, New York, 1969 (also 1945 printing)
  • A.Scharff, 'Synthetic dyestuffs for textiles and their fastness to washing', ICOM-CC Preprints Lyon, Getty Conservation Institute, Los Angeles, 1999 Comment: p.654-660
  • Colour Index International online at www.colour-index.org Comment: developer, date, CAS#=584-42-9, structure verified
  • Sigma Dyes, Stains and Natural Pigments, Infrared Library, Nicolet, 1991-1995 Comment: CAS#=2243-76-7
  • Website: www.straw.com/sig/dyehist