Abstract:
본 발명은 전량 수입에 의존하고 있는 고내광성의 합성섬유를 형광증백제 Cl 혀공 199와 유사한 백도 및 형광능을 지니는 대체 염료로서 하기 구조식(I) 및 (II)의 화합물로 구성된 혼합물을 구입이 용이하고 가격이 저렴한 물질을 원료로 사용하는 간단한 반응 공정에 의해 고순도 및 골수율로 제조하는 새로운 방법에 관한 것이다.
Abstract:
본 발명은 섬유날염용 아조 적색 안료와 이의 제조방법에 관한 것으로서, 더욱 상세하게는 아미노- N -치환된벤즈아미드 유도체를 디아조체로 사용하고 2-하이드록시-3-나프토일 아닐린 유도체를 커플러로 사용하여 상기 두 화합물을 커플링 반응하여 제조하는 다음 화학식 1로 표시되는 섬유날염용 신규 아조 적색 안료와 이의 제조방법에 관한 것이다.
상기 화학식 1에서, A는 C 1 ∼C 4 의 직쇄 또는 측쇄 알킬렌기를 나타내고; R 1 은 수소원자 또는 C 1 ∼C 4 의 알콕시기를 나타내고; R 2 는 수소원자, 염소원자, C 1 ∼C 4 의 알킬기, C 1 ∼C 4 의 알콕시기, 니트로기, 또는 아릴아미드기를 나타낸다.
Abstract:
PURPOSE: Provided are pigment yellow based on quinoxaline which is ecofriendly and has excellent solvent resistance and colorfastness to light, and a method for preparing the same. CONSTITUTION: The pigment yellow based on quinoxaline represented by formula 1 is characterized in that it is prepared using aminoquinoxaline represented by formula 9, as a diazotized compound. In the formulas, R, R1 and R2 are the same or different, and hydrogen, C1-C4 alkyl group, nitro(-NO2), C1-C2 alkoxy group, C1-C18 heterocycle, methyl ester(COOCH3) or halogen group such as chloro or bromo. The pigment yellow is prepared by the steps of (i) diazotizing amino quinoxaline compound represented by formula 9; (ii) dissolving coupler represented by formula 11 into solvent; (iii) mixing two reaction solution obtained from the steps (i) and (ii) at 0-5 deg.C; and (iv) adding base to the solution mixed in the step(iii) to adjust pH to 6-7 with stirring. In the formula 11, R, R1 and R2 are the same as the above.
Abstract:
PURPOSE: Provided is a water-insoluble dispersion reactive dye having a vinyl sulfone reactive group, which dose not contain hazardous amine and metal and can perform dyeing in acidic and neutral condition and has excellent washing fastness and properties. CONSTITUTION: The dispersion reactive dye(formula 2) is produced by diazotizing 2,5-substituted aminophenyl-4-vinyl sulfone(formula 1) and mixing the diazotized 2,5-substituted aminophenyl-4-vinyl sulfone(formula 1) with a coupler at 0-5deg.C and adding a base to separate the produced dye. In the formula, A is methyl or methoxy, R, R1, R2, and R3 are identically or differently selected from hydrogen, alkyl, aminoalkyl, cyanoalkyl, and amino acetyl.
Abstract:
PURPOSE: Provided are benzimidazolone-based yellow pigments which are excellent in solvent resistance and colorfastness to light and provides a high yield, and a method for preparing the same. CONSTITUTION: The benzimidazolone-based yellow pigments represented by formula 1 are characterized in that it is prepared by using amino benzimidazolone represented by formula 9, as a diazotized compound. In the formulas, R, R1 and R2 which are the same or different, are hydrogen, C1-C4 alkyl group, nitro(-NO2) group, C1-C2 alkoxy group, C1-C18 heterocycle, methyl ester(COOCH3) or halogen group such as chloro or bromo. The yellow pigments are prepared by the steps of (i) diazotizing amino benzimidazolone compound represented by formula 9; (ii) dissolving a coupler represented by formula 11 into a solvent; (iii) mixing two solutions obtained from the steps (i) and (ii) at 0-5 deg.C; and (iv) adding base to the solution mixed in the step(iii) to adjust pH to 6-7 with stirring. In the formula 11, R, R1 and R2 are the same as the above.
Abstract:
본발명은삼반응기형청색반응성염료에관한것으로서, 더욱상세하게는한 염료분자내에모노클로로트리아진과두 개의비닐설폰기가반응기로도입되어있어염착률이월등히높아염색폐수가거의발생하지않고, 뿐만아니라염료분자내에적어도한 개의아미노페닐-β-아세톡시에틸설폰반응기가도입되어있어물에대한용해도가낮아염석공정시에소량의염을사용하게되므로폐수처리비용을크게절감시킬수 있고, 염석후 여과시여액으로빠져나가는염료의손실량을최대한줄일수 있는효과를가지는다음화학식 1로표시되는삼반응기형청색반응성염료에관한것이다. 상기화학식 1에서 : Z 및 Z'는서로같거나다른것으로서 OSOM 또는 OCOCH를나타내며, Z 및 Z'중적어도하나는 OCOCH이고,n은 0, 1 혹은 2를나타내며, M은알칼리금속원자를나타낸다.
Abstract:
PURPOSE: A black reactive dye composition useful for cellulose fiber is provided for obtaining excellent endurance efficiency, dying regularity, reproducibility and improving salting-out effect by comprising orange color reactive dye and black color reactive dye each having specified chemical formula in desired content ratio. CONSTITUTION: The black reactive dye composition useful for cellulose fiber having excellent endurance efficiency, dying regularity and reproducibility and salting-out effect comprises the orange color reactive dye having 7-ethoxycarbonyl-amino group of formula 1 and the black color reactive dye having acethoxyethylsulfone or sulfato ethylsulfone reactive groups of formula 2 (wherein Z is -OSO3M or OC(O)CH3; and M represents alkali metal atom) in a weight ratio of 15-35: 65-85 wt.% based on total weight of composition.
Abstract:
PURPOSE: A red reactive dye having two functional groups is provided for lowering water solubility, for having better direct coloring rate to provide vivid colors by introducing aminophenyl-beta-acetoxyethylsulfone functional groups to minimize loss of dye extracted into the filtrate at filtering process and to easily salt-out and reduce the amount of salt required. CONSTITUTION: The red reactive dye represented by formula 1 (wherein M is alkali metal atom) having two functional groups with reduced water solubility and better direct coloring ability in order to reduce loss of dye extracted into the filtrate and to easily salt-out is prepared by condensation reacting 1-naphthol-8-amino-3,6-disulfonic acid and cyanuric chloride; further adding and coupling diazo-reacted 2-naphthylamine-1,5-disulfonic acid; adding the coupling reactant with aminophenyl- beta-acetoxyethylsulfonic compound to carry out condensation reaction.
Abstract:
PURPOSE: A black reactive dye composition having acetoxyethylsulfone reactive group is provided for greatly reducing loss of dye from filtrate at filtering process because of low solubility to water and improving salting-out effect by introducing aminophenyl-beta-acetoxyethylsulfone reactive group to the composition. CONSTITUTION: The black reactive dye composition having the acetoxyethylsulfone reactive group of formula 1 (wherein M represents alkali metal atom) is produced by using the aminophenyl-beta-acetoxyethylsulfone compound of formula 2 as the raw material to form diazo type product; neutralizing 1-naphthol-8-amino-3,6-disulfonic acid compound with any bases; and mixing both of the diazo type material and neutralized material at 0-5 deg.C. and adding the base to control pH7 or less to obtain the final product of formula 1.