Abstract:
The present invention relates to a phenylenediamine based antioxidant compound for bio-diesel and a fabrication method of the same. A phenylenediamine based antioxidant is useful as an antioxidant compound for improving the oxidation stability of the bio-diesel by having high activity on antioxidation because the antioxidant supplies hydrogen to a radical and becomes a phenoxy radical which is stabilized by resonance.
Abstract:
본 발명은 비수용성 유체 제품 식별제로 사용 가능한 아조 염료 및 이의 제조방법에 관한 것으로서, 더욱 상세하게는 N -벤질- N -에틸아닐린을 함유하는 식별제 및 이의 제조방법에 관한 것이다. 본 발명의 N -벤질- N -에틸아닐린을 함유하는 식별제는 비수용성 유체 제품에 높은 용해도를 보이며, 보관 안정성이 우수하고, 미량으로 검출이 가능하며, 비수용성 유체 제품 내에서 산 발색제와 반응하여 뚜렷한 발색을 나타낸다. 따라서, 이러한 식별제를 제품에 첨가시킬 경우, 식별제가 첨가되지 않은 제품과의 구별이 용이하므로, 자사 제품을 타사 제품과 구별하여 유통과정에서의 품질관리를 손쉽게 할 수 있다.
Abstract:
PURPOSE: A yellow azo disperse dye is provided to obtain the same concentration of color even from a small amount of dye when dying because of excellent lightproof, inside sublimability, dispersability, and a high molar extinction coefficient, is also environmentally friendly, and reduces the production costs. CONSTITUTION: A yellow azo disperse dye is indicated as chemical formula 1. In the chemical formula 1, A is selected from the compounds from the chemical formula 1-a. R1-R3 are respectively selected from hydrogen, hydroxyl group, amide group, nitro group, acetyl group, C1-6 alkyl group, C1-6 haloalkyl group, C1-6 alkoxy group, C6-14 aryl group and SO2R7. R4-R6 is respectively selected from hydrogen, C1-6 alkyl group, C1-6 halo alkyl group, C1-6 alkoxy group, nitro group or halogen group. R7 is selected from C1-6 alkyl group, C1-6 alkylamine group, and C6-14 arylamine group or C1-6 acetoxyalkyl group.
Abstract translation:目的:提供黄色偶氮分散染料,即使由于优异的耐光性,内部升华性,分散性和高摩尔消光系数而在染色时由少量的染料得到相同的颜色浓度也是环保的,并且减少了 生产成本。 构成:黄色偶氮分散染料用化学式1表示。在化学式1中,A选自化学式1-a的化合物。 R1-R3分别选自氢,羟基,酰胺基,硝基,乙酰基,C 1-6烷基,C 1-6卤代烷基,C 1-6烷氧基,C 6-14芳基和SO 2 R 7。 R4-R6分别选自氢,C1-6烷基,C1-6卤代烷基,C1-6烷氧基,硝基或卤素基。 R 7选自C 1-6烷基,C 1-6烷基胺基和C 6-14芳基胺基或C 1-6乙酰氧基烷基。
Abstract:
PURPOSE: A method for preparing a novel phthalocyanine compound is provided to easily apply as a pigment for near infrared absorption with high solubility to solvent. CONSTITUTION: A phthalocyanine compound is denoted by chemical formula 1. In chemical formula, R1, R2 and R3 are H, alkyl group of C1-C6; R4 is SO2NR5R6; R5 and R6 are alkyl group of C1-C6 or phenylmethan group; and M is metal atom such as Cu, Zn, Ni or VO. A method for preparing the phthalocyanine compound comprises: a step of dispersing a compound of chemical formula 7 in alcohol; a step of reacting with lithium catalyst under the presence of nitrogen atmosphere to obtain a compound of chemical formula 8; and a step of reacting with a metal of chemical formula 8.
Abstract:
본 발명은 유해아민 또는 중금속을 포함하지 않는 신규 구조의 N -치환된벤즈아미드계 아조 황색 안료와 이의 제조방법에 관한 것으로서, 현재 황색 안료로서 일반적으로 사용되고 있는 피그먼트 엘로우(Pigment Yellow) 12와 비교하여 내용제성, 내약품성 및 내광성 등이 동등하거나 또는 보다 우수하므로 잉크, 도료 등의 산업 분야에서 규제 황색 안료를 대체할 수 있는 새로운 황색 안료로서 유용하다. 유기안료, 아조 황색 안료, 디아조체, 커플러, 아미노-N-치환된벤즈아미드, 내용제성
Abstract:
A method of preparing a D, L-cystine compound is provided to prepare a D, L-cystine compound with high efficiency and high concentration, used for drug additive, permanent medicine, cosmetic material and food nutrition intensifier through chlorination and organic synthesis. A method of preparing a D, L-cystine compound comprises (1) a step for manufacturing dichloro propionitrile indicated as the following chemical formula 3 by performing the chlorination addition of acrylonitrile indicated as the following chemical formula 2; (2) a step for manufacturing a thiazine derivative indicated as the chemical formula 5 by reacting dichloro propionitrile indicated as the chemical formula 3 and thiourea indicated as the chemical formula 4; (3) a step for manufacturing D,L-2-aminothiazoline-4-carboxylic acid indicated as the chemical formula 6 by adding a base to a thiazine derivative indicated as the chemical formula 5; (4) a step for manufacturing a mercapto thiazolidine carboxylic acid indicated as the chemical formula 8 by performing the hydrosulfurization of D,L-2-aminothiazoline-4-carboxy acid indicated as the chemical formula 6 and sodium bisulfide indicated as the chemical formula 7; (5) a step for manufacturing a cystein compound indicated as the chemical formula 9 by hydrolyzing a mercapto thiazolidine carboxylic acid indicated as the chemical formula 8; and (6) a step for manufacturing a cystine compound indicated as the chemical formula 1 by reacting a cystein compound indicated as the chemical formula 9.
Abstract:
A compound for a molecular electronic device with a thiol-based anchoring group is provided to embody a molecular electronic device having a switch characteristic and a memory characteristic by forming a self-assembled molecular active layer between upper and lower electrodes. A dinitrothiophene group is prepared. An aminobenzene group is prepared into which a thiol derivative is introduced. An azo compound having an azo group is connected between the dinitrothiophene group and the aminobenzene group. The aminobenzene group into which the thiol derivative is introduced includes a disulfide group that supplies a ring structure.
Abstract:
PURPOSE: Provided is benzothiazole-based dispersion-reactive dye, which reduces pollution, dose not contain hazardous amine and metals, can be used in acidic and neutral condition, and is excellent in washing-fastness and properties. CONSTITUTION: The benzothiazole-based dispersion-reactive dye represented by the formula 1 is produced by a process comprising the steps of: diazotizing 2-amino-5-(beta-acetoxy ethyl sulfone)benzothiazole or 2-amino-5-(beta-hydroxy ethyl sulfone)benzothiazole; preparing a coupling solution by dissolving a coupler in an acid mixture; mixing the diazotized 2-amino-5-(beta-acetoxy ethyl sulfone)benzothiazole and the coupling solution at 5-10deg.C and adding a base and separating the produced dye or mixing the diazotized 2-amino-5-(beta-hydroxy ethyl sulfone)benzothiazole and the coupling solution at 5-10deg.C and stirring at 80-90deg.C by using acetic anhydride. In the formula, R, R1, R2, and R3 are identically or differently hydrogen, alkyl, alkoxy, cyanoalkyl, or amino acetyl.
Abstract:
PURPOSE: Provided is a water-insoluble dispersion-reactive dye having an acetoxy ethyl sulfone reactive group, which reduces pollution, dose not contain hazardous amine and metals, can be used in acidic and neutral condition, and is excellent in washing-fastness and properties. CONSTITUTION: The dispersion-reactive dye(formula 2) having the 4-aminophenyl-beta-acetoxy ethyl sulfone reactive group(formula 1) is produced by a process comprising the steps of: diazotizing the 4-aminophenyl-beta-acetoxy ethyl sulfone(formula 1); making a coupling solution by dissolving a coupler in water and concentrated hydrochloric acid; mixing the diazotized 4-aminophenyl-beta-acetoxy ethyl sulfone with the coupling solution at 0-5deg.C; adding a base to keep pH neutral condition and separating the produced dye. In the formula, R, R1, R2, and R3 are identically or differently hydrogen, alkyl, alkoxy, cyanoalkyl, amino acetyl, and amino ester.