The novel yellow metal azo pigments based on at least three metal azo compounds which differ at least in the type of metal have improved color strengths and are of excellent suitability for pigmentation of pigment preparations for a broad field of use.

The novel yellow metal azo pigments based on at least three metal azo compounds which differ at least in the type of metal have improved color strengths and are of excellent suitability for pigmentation of pigment preparations for a broad field of use.

Disclosed herein is a tricyclic octacationic cyclophane and complexes comprising the tricyclic octacationic cyclophane and a perylene diimide dye complexed therein and methods of using and making the cyclophane and complexes.

Yellow metal azo pigments based on adducts of at least two metal azo compounds provide improved dispersion properties and are of excellent suitability for pigmentation of pigment preparations for a broad field of use.

A C.I. Pigment Yellow 74 as an insoluble azo pigment is provided. This C.I. Pigment Yellow 74 is crystalline particles. The ratio (26.6/11.7) of a diffraction intensity of a peak at 26.6 to a diffraction intensity of a peak at 11.7 in terms of Bragg angle (20.2) as measured by powder X-ray diffraction using CuK -radiation is 0.85 to 1.12, and the average primary particle size is 20 to 130 nm. The use of this C.I. Pigment Yellow 74 as a colorant in a coloring composition enables to provide the coloring composition with excellent dispersibility and good particle size stability and storage stability compared with conventional pigments. The use of this coloring composition enables the formation (recording) of images having excellent clarity and transparency of such high levels that have not been achievable by conventional technologies.

This invention relates to an improved method for the preparation of highly or substantially pure Indigotindisulfonate sodium (1). It further relates to the novel crystalline form I of Indigotindisulfonate sodium (1) and the process for its preparation.

A novel method for the preparation of indocyanine green. The method involves converting 4-[2-[7-[1, 1-dimethyl-3-(4-sulfobutyl)benzo[e]indol-3-ium-2-yl]hepta-2,4,6-trienylidene]-1,1-dimethylbenzo[e]indol-3-yl]butane-1-sulfonic acid to indocyanine green by treatment with sodium chloride. A crystalline form of indocyanine green is also described, along with a, pharmaceutical compositions comprising the same, and to methods of using the same as a medicament or a diagnostic agent.

The present invention is a crystal of 3-(3-{[3-(cyclomaltoheptaos-21-O-yl)propyl]amino}-3-oxopropyl)-2-{(1E)-2-[(3E)-3-{(2E)-2-[3-(3-{[3-(cyclomaltoheptaos-21-O-yl)propyl]amino}-3-oxopropyl)-1,1-dimethyl-1,3-dihydro-2H-benzo[e]indol-2-ylidene]ethylidene}-2-methoxycyclohex-1-en-1-yl]ethen-1-yl}-1,1-dimethyl-1H-benzo[e]indol-3-ium chloride.