Arylide

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Description

A class of synthetic yellow, orange and red organic colorants. These insoluble direct azo dyes were first synthesized from aniline-based diazonium salts and acetoacetarylide in 1909. Arylide was sold commercially as Hansa yellow by Hoechst AG in 1915. Arylide yellows have good tinting strength, opacity and solvent resistance. They have good lightfastness and are primarily used in printing inks, plastic, rubbers, as well as architectural and artists paints. Monoarylide yellows have better lightfastness than diarylides.

Synonyms and Related Terms

monoarylide; diarylide; azo dye; monoazo dye; Hansa yellow; colorante azoico (Esp.); colorante azoico (It.)

FTIR PY001(MFA)

PY001 sun arylide yellow 272-0008.TIF

FTIR PY003(MFA)

PY003 sun arylide yellow 272-3119.TIF

FTIR PY062(MFA)

PY062 sun arylide yellow calcium salt 262-3562.TIF

FTIR PY074(MFA)

PY74 kremer23650.TIF

Comparisons

PY065 sun arylide yellow 272-0065.TIF

Pigment number Manufacture Pigment name Manufacture CI number Comments
PY001 Sun arylide yellow 272-0008
PY003 Sun arylide yellow 272-3119
PY062 Sun arylide yellow 262-3562
PY065 Sun arylide yellow 272-0065
PY074 Kremer unspecified 23650

Other Properties

Most arylide dyes are soluble in organic solvents. Resistant to water, oil, acids and bases.

Melting Point 150 (dec)

Hazards and Safety

May bleed in paints. Decomposes at temperatures over 150 C.

Potential carcinogen.

Additional Information

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

  • 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
  • Website address 1 Comment: www.handprint.com

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