2-[[1-[[(2,3-dihydro-2-oxo-1H-benzimidazol-5-yl)amino]carbonyl]-2-oxopropyl]azo]-benzoic acid and a process for its preparation
AssigneeBASF SE
InventorsHans Reichert, Max Hügin, Ulrich Veith, Sibylle Soder, Thomas Eichenberger
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Abstract
The present invention is directed to 2-[[1-[[(2,3-dihydro-2-oxo-1H-benzimidazol-5-yl)amino]carbonyl]-2-oxo-propyl]azo]-benzoic acid (C.I. Pigment Yellow 151): (I), characterized by a ΔE* (black/white) in masstone below 22.0±0.7, a process for its preparation and its use for pigmenting macromolecular organic materials of natural or synthetic origin. The pigment has high opacity and high color strength.
Claims6
2-[[1-[[(2,3-dihydro-2-oxo-1H-benzimidazol-5-yl)amino]carbonyl]-2-oxopropyl]azo]-benzoic acid
- having a cubic, or a cuboidal particle form, and a ΔE* (black/white) in masstone below 22.0±0.7.
2-[[1-[[(2,3-dihydro-2-oxo-1H-benzimidazol-5-yl)amino]carbonyl]-2-oxopropyl]azo]-benzoic acid
- having a cubic, or a cuboidal particle form, and a ΔE* (black/white) in masstone below 22.0±0.7, wherein the color strength of the compound is 6 to 55%, higher than the color strength of C. I. Pigment Yellow 151 HOSTAPERM Yellow H4G (Clariant AG) as standard in white reduction (5:95).
A process for the manufacture of the compound of the formula
- comprising coupling of diazotized anthranilic acid (1-aminobenzene-2-carboxylic acid) with 5-acetoacetylamino-benzimidazolone in an aqueous medium and a thermal after-treatment, wherein the thermal after-treatment is carried out at a pH of from 6.0-7.3 at a temperature of from 90 to 110° C.
Dependencies are inferred from the claim text.