Patent classifications
C09B67/0034
WAVELENGTH SELECTIVE ABSORPTION FILTER, POLARIZING PLATE, ORGANIC ELECTROLUMINESCENT DISPLAY DEVICE, AND LIQUID CRYSTAL DISPLAY DEVICE
Provided are a wavelength selective absorption filter containing a resin and a dye A, which has a main absorption wavelength band in the wavelength selective absorption filter at a wavelength of 400 to 450 nm, and a dye C, which has a main absorption wavelength band in the wavelength selective absorption filter at a wavelength of 560 to 600 nm, each of which has a main absorption wavelength band in a different wavelength range, as well as a polarizing plate and an organic electroluminescent display device or liquid crystal display device, which include the wavelength selective absorption filter. However, the dye A and the dye C do not have fluorescence.
Triaryl methane composition, dye composition for ocular membrane dyeing
A composition containing Brilliant Blue G (BBG) or a pharmaceutically acceptable salt thereof, and a positional isomer of Brilliant Blue G (BBG) or a pharmaceutically acceptable salt thereof, the composition containing 90 wt % or more and 100 wt % or less of one or both of Brilliant Blue G (BBG) and the pharmaceutically acceptable salt thereof in the total of the Brilliant Blue G (BBG), the pharmaceutically acceptable salt of Brilliant Blue G (BBG), the positional isomer of Brilliant Blue G (BBG), and the pharmaceutically acceptable salt of the positional isomer of Brilliant Blue G (BBG), a method for producing said composition, and a method of removing the ocular membrane of a human patient.
OPTICAL FILM FORMING COMPOSITION, OPTICAL FILM, AND DISPLAY DEVICE INCLUDING SAME
The present specification relates to a composition for forming an optical film comprising a compound represented by Chemical Formula 1 and a binder resin, an optical film, and a display device comprising the same.
Composition, film, near infrared cut filter, solid-state imaging element, image display device, and infrared sensor
A composition includes a near infrared absorbing pigment and a solvent, in which the near infrared absorbing pigment is at least one selected from a colorant compound which has a cation and an anion in the same molecule, a colorant compound which is a salt of a cationic chromophore and a counter anion, and a colorant compound which is a salt of an anionic chromophore and a counter cation, a D50 particle size in which a cumulative volume in a particle size distribution of particle sizes of the near infrared absorbing pigment is 50% is 100 nm or lower, and d values of Hansen solubility parameters of the near infrared absorbing pigment and the solvent satisfy a predetermined expression.
ISOINDOLINE DERIVATIVES
An isoindoline derivative of formula
##STR00001##
wherein
X is N, C—CN or C—COR.sup.2;
Y is a radical having an acidic group or a basic group;
R.sup.1 is independently from one another halogen or C.sub.1-C.sub.4-alkyl, said alkyl is unsubstituted or substituted with halogen;
R.sup.2 is C.sub.1-C.sub.4-alkyl, said alkyl is unsubstituted or substituted with halogen; and
n is 0, 1, 2, 3 or 4,
with the proviso that Y does not include an acidic group if X is C—CN or C—COR.sup.2, and compositions containing the same are provided. The isoindoline derivative and the pigment composition are suitable, for example, for coloring high molecular mass organic material, especially paints, printing inks, resist formulations for color filter applications, electrophotographic toners, cosmetics, plastics, films or fibers.
Pigment composition, method for producing thereof, and aqueous ink composition
A pigment composition including at least one pigment selected from the group consisting of a perinone-based pigment and a perylene-based pigment, water, a resin having a constitutional unit represented by Formula 1, and at least one compound selected from the group consisting of a phthalimide compound having a carboxyalkyl group and a naphthalimide compound having a carboxyalkyl group; a method for producing thereof; and an aqueous ink composition using the pigment composition. In Formula 1, R.sup.1 represents a hydrogen atom or a methyl group, L.sup.2 represents —C(═O)O—, —OC(═O)—, or —C(═O)NR.sup.2— and R.sup.2 represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, and R.sup.3 represents an alkyl group having 6 or more carbon atoms. ##STR00001##
Dye composition comprising a combination of natural dyeing agents including an extract of <i>Lawsonia inermis</i>
The disclosure relates to a dye composition comprising a combination of natural dyeing agents including an extract of Lawsonia inermis. The disclosure also relates to the cosmetic use of said composition for dyeing keratin fibers. The disclosure also relates to a cosmetic method for dyeing keratin fibers comprising the application of such a composition.
Photosensitive resin composition, photosensitive resin layer using the same and color filter
A photosensitive resin composition, a photosensitive resin layer, and a color filter, the composition including a colorant including a first green dye having a core-shell structure and a second green dye in a weight ratio of about 1:9 to about 7:3; a binder resin; a photopolymerizable compound; a photopolymerization initiator; and a solvent.
COLOR PAINTS TAILORED FOR SOLAR HEAT MANAGEMENT
This disclosure provides cool paints and paint systems tailored for solar heat management comprising (a) hydroxyl-containing fluorocarbon polymer as binder, (b) an effect pigment, and (c) an IR transparent pigment. Specifically, the dark color paints exhibit higher than 40% total solar reflectance (TSR) and excellent weathering properties e.g., maintaining at least 80% gloss after two-year of exposure to solar irradiation in field test.
Process for the Purification of Methylene Blue
The present application provides method for producing methylene blue that includes the steps of providing a reaction mixture having one or more methylene blue intermediates; precipitating metal from the reaction mixture; and producing therefrom crude methylene blue. The crude may further be purified, resulting in methylene compounds having low impurities, preferably having a purity greater than about 97%, having Azure B impurity no greater than 2.5%, and/or a total metal content no greater than 77 ppm. Formulations containing such compounds are also provided.