摘要:
The present invention provides a safe charge control agent which exhibits an excellent negative chargeability and excellent dispersibility in and compatibility with binder resins, and is even applicable for col or toners. Specifically, the charge control agent consists of a naphthol derivative of formula [I]: and a salt thereof, and an electrophotographic toner comprising the agent are provided.
摘要:
The present invention provides novel condensed azo compounds using bisamide compounds of 2-hydroxynaphthalene-3,6-dicarboxylic acid, amide, or ester as the couplers, which have excellent properties such as excellent water resistance, chemical resistance, solvent resistance, and heat resistance.
摘要:
The present invention provides a method for producing a hydroxybenzoic acid compound comprising, dehydrating a phenol compound and an alkaline metal compound to form the alkaline metal salt of the phenol compound and reacting the alkaline metal salt and carbon dioxide, wherein the dehydrating step is conducted by reacting the alkaline metal compound with an excess amount of the phenol compound at a temperature of 160° C. or above. According to the method of the present invention, the hydroxybenzoic acid compound can be obtained by simple steps with low cost without using an expensive aprotic polar organic solvent. The provided method can produce highly pure hydroxybenzoic acid compound comprising little by-products in high yield.
摘要:
A monoazo compound synthesized using 2-hydroxynaphthalene-3,6-dicarboxylic acid (or salt thereof), an amide, an ureide or an ester thereof as a coupler is novel, and is superior in water resistance, chemical resistance and solvent resistance. The present invention provides such a novel azo compound and a process for producing the same.
摘要:
The present invention provides a method for producing a naphthalenecarboxylic acid amide compound represented by formula [1] comprising, reacting a naphthalenecarboxylic acid halide compound represented by formula [2] with ammonium acetate in a solvent having an ether bond. According to the method of the present invention, a naphthalene carboxylic acid amide compound can be obtained at high yield and at low cost.
摘要:
The present invention provides a process for preparing 3-nitro-4-alkoxybenzoic acid, which comprises the step of subjecting a mixture comprising 4-alkoxybenzoic acid and 40-80% nitric acid, wherein the amount of the 40-80% nitric acid is equal to or more than 8 times that of 4-alkoxybenzoic acid by weight, to a reaction at a temperature of 30-100° C.
摘要:
The present invention provides a hydroxynaphthalenedicarboxylic acid hydrazide or a derivative thereof represented by formula (1): wherein X1 is a group selected from the group consisting of carboxyl group, a group represented by formula (2) and a group represented by formula (3): —CO—NH-Z (2) —CO—NHNH2 (3) Y1 is a group selected from the group consisting of carboxyl group, carbamoyl group, a group represented by formula (2), a group represented by formula (3) and a group represented by formula (4): —CO—O-A (4) provided that at least one of X1 and Y1 is a group represented by formula (3).
摘要:
The present invention provides an aminocarbonylnaphthol derivative represented by formula (1) and process for preparing the same: wherein each Y1 and Y2 is selected from the group consisting of aminocarbonyl group, carboxyl group and groups represented by formulae (2), (3) and (4), provided that at least one of Y1 and Y2 is aminocarbonyl group. The present invention also provides a novel cyanonaphthol derivative represented by formula (7) and a salt thereof as well as process for preparing them: wherein each Y7 and Y8 is independently selected from the group consisting of cyano group, groups represented by formulae (2), (3) and (4), carboxyl group and aminocarbonyl group, provided that at least one of Y7 and Y8 is cyano group.
摘要:
Disclosed is a method for preparing a 2-hydroxy-6-ureidocarbonyl naphthalene derivative. The method comprises the step of reacting 2-hydroxy-6-aminocarbonyl naphthalene and a isocyanate in an organic solvent at a temperature of 90–200° C. According to the present invention, 2-hydroxy-6-ureidocarbonyl naphthalene derivative can easily be obtained within relatively short time and high yield.