This color contains the following pigments:
Benzimidazolone Orange is a reddish orange pigment that can lose its intensity and become dull in tints. It has an average drying time.
Benzimidazolone Orange has excellent lightfastness and outstanding heat and solvent stability for a monoazo pigment.
Benzimidazolone Orange is not considered toxic.
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.
Bis-(p-chrolopheny)-1. 4-diketopyrrolo(3. 4-c)pyrrole
Pyrrole Red is opaque and has strong covering power. According to manufacturer Ciba, which uses the trade name Irgazin Red, it is a “clean, highly saturated mid shade red with high temperature resistance, excellent color strength, outstanding chemical, solvent and bleed resistance, and good weatherfastness.”
Pyrrole Red is considered to have excellent lightfastness among organic pigments in its class. Tests in industrial applications have given it scores of 7-8 on the Blue Wool Scale.
According to the Australian government's Ministry on Health and Aging, "The notified chemical exhibited low oral and dermal toxicity in rats, did not exhibit toxic effects when administered orally to rats for 28 days, was not a skin irritant in rabbi
Pyrrole Red, used as an automotive paint and as a colorant in plastics, was developed as one of a range of pigments to replace lead based pigments. In art materials, it is often used as a synthetic and lightfast replacement for carmine, a laked pigment that was originally produced from the body of the cochineal insect. It is also used to replace the older naphthol reds, organic red pigments that are sometimes only marginally lightfast and weatherfast.