C09B31/02

REACTION ACCELERATING AGENT
20190300929 · 2019-10-03 · ·

Provided is a compound capable of accelerating the enzymatic reaction catalyzed by peroxidase. The present invention provides a peroxidase reaction accelerating agent comprising a compound represented by formula (I) and a method for measuring hydrogen peroxide using the same.

Color polarizing film, antireflective film and display device

A color polarizing film including a first layer including a first polymer and a first dichroic dye having an absorption wavelength region of about 380 nm to about 780 nm and a second layer including a second polymer and a second dichroic dye having an absorption wavelength region of about 380 nm to about 780 nm, wherein the second layer is disposed on the first layer, wherein a polarization axis of the first layer and a polarization axis of a second layer cross each other, and wherein the color polarizing film exhibits a maximum absorption wavelength (?.sub.max) in a wavelength range of about 380 nm to about 780 nm.

Color polarizing film, antireflective film and display device

A color polarizing film including a first layer including a first polymer and a first dichroic dye having an absorption wavelength region of about 380 nm to about 780 nm and a second layer including a second polymer and a second dichroic dye having an absorption wavelength region of about 380 nm to about 780 nm, wherein the second layer is disposed on the first layer, wherein a polarization axis of the first layer and a polarization axis of a second layer cross each other, and wherein the color polarizing film exhibits a maximum absorption wavelength (?.sub.max) in a wavelength range of about 380 nm to about 780 nm.

LOW TOXICITY INK FORMULATIONS WITH IMPROVED PRINTHEAD LIFETIME
20180298218 · 2018-10-18 ·

An inkjet ink includes: (i) a disazo dye of formula (I):

##STR00001##

(ii) 1,3-propanediol; (iii) a glycol compound selected from the group consisting of: triethylene glycol and tetraethylene glycol; and (iv) water. The ink has low toxicity and is preferably absent ethylene glycol and sulfolane.

Bis-Azo Colorants for Use as Bluing Agents

This invention relates to bis-azo colorants for use as bluing agents, laundry care compositions comprising bis-azo colorants that may serve as bluing agents, processes for making such bluing agents and laundry care compositions and methods of using the same. The bluing agents are generally comprised of at least two components: at least one chromophore component and at least one polymeric component. These bluing agents are advantageous in providing a whitening effect to fabrics, while not building up over time and causing undesirable blue discoloration to the treated fabrics.

Bis-azo colorants for use as bluing agents

This invention relates to bis-azo colorants for use as bluing agents, laundry care compositions comprising bis-azo colorants that may serve as bluing agents, processes for making such bluing agents and laundry care compositions and methods of using the same. The bluing agents are generally comprised of at least two components: at least one chromophore component and at least one polymeric component. These bluing agents are advantageous in providing a whitening effect to fabrics, while not building up over time and causing undesirable blue discoloration to the treated fabrics.

Chiral azobenzene dopants with increased delta helical twisting power

A chiral azobenzene dopant with helical twisting power has a structure represented by the following formula (I): ##STR00001##
wherein Z and Z are independently selected from the group consisting of naphthalene and phenanthrene; when Z or Z is naphthalene, the naphthalene optionally has R.sub.3 at the 6 position and R.sub.4 at the 6 position; when Z or Z is phenanthrene, the phenanthrene optionally has R.sub.3 at the 7 position and R.sub.4 at the 7 position; R.sub.1, R.sub.2, R.sub.3, and R.sub.4 are independently selected from the group consisting of an alkyl group having 1 to 20 carbons, an alkoxy group having 1 to 20 carbons, an aryl group having 6 to 20 carbons, and an aryloxy group having 6 to 20 carbons; and on any R.sub.1, R.sub.2, R.sub.3, and R.sub.4, on any CH.sub.2 a CH.sub.3 is optionally attached by replacing a hydrogen on a CH.sub.2.

COLOR POLARIZING FILM, ANTIREFLECTIVE FILM AND DISPLAY DEVICE

A color polarizing film including a first layer including a first polymer and a first dichroic dye having an absorption wavelength region of about 380 nm to about 780 nm and a second layer including a second polymer and a second dichroic dye having an absorption wavelength region of about 380 nm to about 780 nm, wherein the second layer is disposed on the first layer, wherein a polarization axis of the first layer and a polarization axis of a second layer cross each other, and wherein the color polarizing film exhibits a maximum absorption wavelength (.sub.max) in a wavelength range of about 380 nm to about 780 nm.

COLOR POLARIZING FILM, ANTIREFLECTIVE FILM AND DISPLAY DEVICE

A color polarizing film including a first layer including a first polymer and a first dichroic dye having an absorption wavelength region of about 380 nm to about 780 nm and a second layer including a second polymer and a second dichroic dye having an absorption wavelength region of about 380 nm to about 780 nm, wherein the second layer is disposed on the first layer, wherein a polarization axis of the first layer and a polarization axis of a second layer cross each other, and wherein the color polarizing film exhibits a maximum absorption wavelength (.sub.max) in a wavelength range of about 380 nm to about 780 nm.

Chiral Azobenzene Dopants with Increased Delta Helical Twisting Power

A chiral azobenzene dopant with helical twisting power has a structure represented by the following formula (I):

##STR00001##

wherein Z and Z are independently selected from the group consisting of naphthalene and phenanthrene; when Z or Z is naphthalene, the naphthalene optionally has R.sub.3 at the 6 position and R.sub.4 at the 6 position; when Z or Z is phenanthrene, the phenanthrene optionally has R.sub.3 at the 7 position and R.sub.4 at the 7 position; R.sub.1, R.sub.2, R.sub.3, and R.sub.4 are independently selected from the group consisting of an alkyl group having 1 to 20 carbons, an alkoxy group having 1 to 20 carbons, an aryl group having 6 to 20 carbons, and an aryloxy group having 6 to 20 carbons; and on any R.sub.1, R.sub.2, R.sub.3, and R.sub.4, on any CH.sub.2 a CH.sub.3 is optionally attached by replacing a hydrogen on a CH.sub.2.