Color Swatch created using full strength/50/50 and was applied on acrylic primed canvas (7 oz) material.
This color contains the following pigments:
PO36—Benzimidazolone Orange
Pigment Type
organic, monoazo
Chemical Name
n/a
Chemical Formula
C17H13ClN6O5
Properties
Benzimidazolone Orange is a reddish orange pigment that can lose its intensity and become dull in tints. It has an average drying time.
Permanence
Benzimidazolone Orange has excellent lightfastness and outstanding heat and solvent stability for a monoazo pigment.
Toxicity
Benzimidazolone Orange is not considered toxic.
History
The benzimidazolone group of pigments was developed and patented in 1960 by Hoechst A.G., a German chemical manufacturer that was a forerunner of the pharmaceutical company Aventis. Use of benzimidazolone pigments in the auto industry, especially Benzimidazolone Orange, became common in the 1980s because they were common replacements for lead chromate pigments, which were phased out during this period.
Alternate Names
n/a
PY151—Benzimidazolone Yellow
Pigment Type
oranic, monoazo
Chemical Name
n/a
Chemical Formula
n/a
Properties
Benzimidazolone Yellow is a greenish yellow pigment with dull tints and an average drying time. It mixes very cleanly. It mixes cleanly with both Phthalo Green and Titanium White. Although more expensive than many Hansa and Diarylide pigments, its mixing properties, durability, and lightfastness have won it many customers.
Permanence
Benzimidazolone Yellow has excellent lightfastness and durability. This has made it an extremely important pigment in the printing industry, for applications where lightfastness is a primary consideration. Though it is not absolutely lightfast, it ranks extremely well among organic yellows.
Toxicity
Benzimidazolone Yellow is not considered toxic.
History
The benzimidazolone group of pigments was developed and patented in 1960 by Hoechst A.G., a German chemical manufacturer that was a forerunner of the pharmaceutical company Aventis.
Alternate Names
Benzimidazolone.
