KR940000529A - Reactive dye composition and dyeing or printing method using the same - Google Patents
Reactive dye composition and dyeing or printing method using the same Download PDFInfo
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- KR940000529A KR940000529A KR1019930011663A KR930011663A KR940000529A KR 940000529 A KR940000529 A KR 940000529A KR 1019930011663 A KR1019930011663 A KR 1019930011663A KR 930011663 A KR930011663 A KR 930011663A KR 940000529 A KR940000529 A KR 940000529A
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Abstract
본 발명은 셀룰로스계 섬유 재료 또는 셀룰로스계 섬유를 함유하는 섬유재료를 균일하게, 선명하고 진한 색으로 그리고 견뢰하게 염색 및 날염할 수 있는 적색 반응 염료를 재공한다. 본 발명은 유리산 형태는 하기 일반식 (I)로 표시되는 1종 이상의 영료와The present invention provides a red reactive dye capable of dyeing and printing the cellulosic fibrous material or the fibrous material containing the cellulosic fibers uniformly, vividly, darkly and reliably. In the present invention, the free acid form includes one or more kinds of fillers represented by the following general formula (I)
(상기 식에서, m은 0또는 1이고: R1은 수소원자, 저급알킬기 또는 저급 알콕시기이며: R2및 R3는 각기 독립하여 수소원자, 또는 히드록실기, 시아노기, 알콕시기, 카르복시기. 카르바모일기. 알콕시카르보닐기, 알킬카르보닐옥시기, 술포기, 술파모일기 또는 할로겐 원자로 치환되거나 또는 비치환된 저급 알킬기이고; A는 저급 알킬기, 저급 알륵시기, 술포기 또는 할로겐 원자중의 하나 또는 두개의 치환기로 치환되거나 또는 비치환된 페닐렌기, 또는 나프틸렌기 또는 술포나프틸렌기이고: X1은 할로겐 원자, -N(R4)R5, 또는 -OR6(여기에서 R4, R5,및 R6는 각기 독립하여 수소원자, 또는 히드록실기, 시아노기, 알콕시기. 카르복시기, 카르바모일기, 알콕시카르보닐기, 알킬카르보닐옥시기, 술포기, 술파모일기, 또는 할로겐 원자로 치환되거나 또는 비치환된 알킬기, 페닐기 또는 나프틸기입)이고: Y1은 -SO2CH=CH2기 또는 -SO2CH2CH2Z1R6기(여기에서, Z1,은 알칼리의 작용에 의해 분리 가능한 기임)이다.] 유리산의 형태로는 하기 일반식(ll)로 표시되는 1종 이상의 염료:(Wherein m is 0 or 1, R 1 is a hydrogen atom, a lower alkyl group or a lower alkoxy group: R 2 and R 3 are each independently a hydrogen atom, or a hydroxyl group, a cyano group, an alkoxy group, a carboxyl group). A carbamoyl group, an alkoxycarbonyl group, an alkylcarbonyloxy group, a sulfo group, a sulfamoyl group or a lower alkyl group unsubstituted or substituted with a halogen atom; A is one of a lower alkyl group, a lower alkoxy group, a sulfo group or a halogen atom or A phenylene group unsubstituted or substituted with two substituents, or a naphthylene group or a sulfonafthylene group: X 1 is a halogen atom, —N (R 4 ) R 5 , or —OR 6 (where R 4 , R 5 and R 6 are each independently substituted with a hydrogen atom or a hydroxyl group, a cyano group, an alkoxy group, a carboxyl group, a carbamoyl group, an alkoxycarbonyl group, an alkylcarbonyloxy group, a sulfo group, a sulfamoyl group, or a halogen atom, or Or rain Substituted alkyl, phenyl or naphthyl): Y 1 is a -SO 2 CH = CH 2 group or -SO 2 CH 2 CH 2 Z 1 R 6 group (wherein Z 1 , is separated by the action of an alkali) One or more dyes represented by the following general formula (ll) in the form of the free acid:
(상기 식에서, n은0, 1또는 2이고, Wl및 W2는 그중 어느 하나가수소원자이면, 다른 하나는 술포기이고: R2은 수소원자, 또는 히드록실기, 시아노기, 알콕시기, 카르복시기, 카르바모일기, 알콕시카르보닐기, 알킬카르보닐옥시기, 술포기, 술파모일기 또는 할로긴 원자로 치환되거나 또는 비치환된 저급 알킬기이고, B는 저급 알킬기, 저급 알록시기, 술포기 또는 할로겐 원자중의 하나 또는 두개의 치환기로 치환되거나 또는 비치환된 페닐렌기, 또는 나프틸렌기 또는 술포나프틸렌기이고: R2는 -N(R8)R9, -OR10(여기에서 R8,R9,및 R10는 각기 독립하여 수소원자, 또는 히드록실기, 시아노기, 알콕시기, 카르윤시기, 카르바모일기, 알콕시카르보닐기, 알킬카르보닐 옥시기, 술포기, 술파모일기, 또는 할로겐 원자로 치환되거나 또는 비치환된 알킬기, 페닐기 또는 나프틸기, 또는 치환되거나 또는 비치환된 피리디니오기, 모르폴리노기 또는 피페리지노기)이고: Y2는 -S02CH=CH2또는 -S02CH2CH2Z1기(여기에서, Z2은 알칼리의 작용에 의해 분리 가능한 기임)이다. ]로 이루어진 반웅성 염료 조성물이 제공된다.(Wherein n is 0, 1 or 2, and W 1 and W 2 are either hydrogen atoms, the other is a sulfo group: R 2 is a hydrogen atom, or a hydroxyl group, a cyano group, an alkoxy group) , A carboxyl group, a carbamoyl group, an alkoxycarbonyl group, an alkylcarbonyloxy group, a sulfo group, a sulfamoyl group or a lower alkyl group unsubstituted or substituted with a halogin atom, B is a lower alkyl group, a lower alkoxy group, a sulfo group or a halogen atom Is a phenylene group unsubstituted or substituted with one or two substituents, or a naphthylene group or a sulfonaphthylene group: R 2 is —N (R 8 ) R 9 , -OR 10 , wherein R 8 , R 9 and R 10 are each independently substituted with a hydrogen atom or a hydroxyl group, a cyano group, an alkoxy group, a carboxy group, a carbamoyl group, an alkoxycarbonyl group, an alkylcarbonyl oxy group, a sulfo group, a sulfamoyl group, or a halogen atom Or unsubstituted alkyl groups, phenyl Or a naphthyl group, or a substituted or unsubstituted or unsubstituted come flutes dini, morpholino group or a piperazinyl group ridges), and: Y 2 in the group -S0 2 CH = CH 2 or -S0 2 CH 2 CH 2 Z 1 ( here, Z 2 is a group that can be separated by the action of an alkali).
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.
Claims (7)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP92-193234 | 1992-06-26 | ||
JP19323492A JP3198635B2 (en) | 1992-06-26 | 1992-06-26 | Reactive dye mixture and dyeing or printing method using the same |
JP92-172788 | 1992-06-30 | ||
JP4172788A JPH0615446A (en) | 1992-06-30 | 1992-06-30 | T-shaped butting arc welding method for bar steel and apparatus therefor |
Publications (1)
Publication Number | Publication Date |
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KR940000529A true KR940000529A (en) | 1994-01-03 |
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Application Number | Title | Priority Date | Filing Date |
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KR1019930011663A KR940000529A (en) | 1992-06-26 | 1993-06-25 | Reactive dye composition and dyeing or printing method using the same |
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KR (1) | KR940000529A (en) |
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1993
- 1993-06-25 KR KR1019930011663A patent/KR940000529A/en active IP Right Grant
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