CN101230203A - High light-fast red reactive dye and preparation method thereof - Google Patents

High light-fast red reactive dye and preparation method thereof Download PDF

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Publication number
CN101230203A
CN101230203A CNA2007103024830A CN200710302483A CN101230203A CN 101230203 A CN101230203 A CN 101230203A CN A2007103024830 A CNA2007103024830 A CN A2007103024830A CN 200710302483 A CN200710302483 A CN 200710302483A CN 101230203 A CN101230203 A CN 101230203A
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China
Prior art keywords
acid
phenylene diamine
sulfonic acid
ortho
red reactive
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CNA2007103024830A
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Chinese (zh)
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褚平忠
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Individual
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Individual
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Priority to CNA2007103024830A priority Critical patent/CN101230203A/en
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Abstract

The invention discloses high sun-proof red reactive dye and the preparation method thereof. Tricyanogen chloride is unipolycondensated with m-Phenylene diamine-4,6-ortho sulfonic acid, m-Phenylene diamine-4,6-disulfonic acid or p-phenylene diamine-ortho sulfonic acid, and then copolycondensated with para position or meta position ester compound, and then diazotized and coupled with 2R acid or gamma acid; tricyanogen chloride is unipolycondensated with para position or meta position ester compound, and then copolycondensated with m-Phenylene diamine-4,6-ortho sulfonic acid, m-Phenylene diamine-4,6-disulfonic acid or p-phenylene diamine-ortho sulfonic acid, and then diazotized and coupled with 2R acid or gamma acid; the high sun-proof red reactive dye has good building up property, level dyeing property, color fixation rate and high combination stability of fiber and dye, and has good light fastness. The additive property of mixed color matching dye mixture further enhances the dying appetence and the color fixation rate, to ensure the dying effect to be more outstanding. The invention is suitable for the dying of natural cellulose such as cotton, viscose fiber and blended fiber.

Description

Red reactive dyes of high light-fast and preparation method thereof
Technical field
The present invention relates to red reactive dyes of a kind of high light-fast and preparation method thereof.
Background technology
Along with the users of dyeing are more and more high to reactive dyestuffs requirement to its light fastness in dyeing course, yellow dyes and blue dye all have the comparatively satisfied kind of light fastness in the kind of reactive dyestuffs at present, red exactly kind can not satisfy user's demand, and pressing for dyestuff manufactory can provide light fastness red preferably kind.
Summary of the invention
In order to solve light fastness orchil kind preferably, the invention provides red reactive dyes of high light-fast and preparation method thereof.
The red reactive dyes of a kind of high light-fast of the present invention, its structure is as follows:
Figure S2007103024830D00011
A 1Be C 1
B 1For
Figure S2007103024830D00012
Or
Figure S2007103024830D00013
Figure S2007103024830D00021
A 2Be C 1
B 2For
Figure S2007103024830D00022
M is 1 or 2
Figure S2007103024830D00023
A 3Be C 1
B 3For
Figure S2007103024830D00024
Or
Figure S2007103024830D00025
N is 1 or 2
With B 1For not isoplastic dyestuff (1) mixes colorant match, perhaps dyestuff (2) is mixed colorant match with dyestuff (3).
Its method is:, path 1: cyanuric chloride and mphenylenediamine ortho-sulfonic acid, mphenylenediamine disulfonic acid or Ursol D ortho-sulfonic acid one contract, then and contraposition or a bit esterified thing two contract diazotization and 2R acid or γ acid coupling and getting again; Can also contract by cyanuric chloride and contraposition or a bit esterified thing one, contract with mphenylenediamine ortho-sulfonic acid or mphenylenediamine disulfonic acid or Ursol D ortho-sulfonic acid two again, again diazotization and 2R acid or γ acid coupling and getting.
For the purpose of the anionic group of dyestuff of the present invention was convenient, they all existed with the sour form acid of freedom form, when existing in the water soluble salt mode when making and use, exist with sodium salt or potassium salt form especially.
The present invention goes out the orchil composition of array structure down, it is applicable to the dyeing of natural cellulose such as cotton, viscose fiber and mixed fibre, it has good enhancing and level-dyeing property, in addition, higher degree of fixation, fiber-dyestuff bonded high stability, wash resistant, fastness to light and good photostabilization are still arranged, and fastness shows Exposure to Sunlight, the sweat day light fastness of light color especially.And utilize composite technology to utilize the further painted avidity of raising of additivity and the degree of fixation of two or more dye mixture to make its Color more excellent.
Embodiment:
Specific implementation method:
Embodiment one: contract: contract in one and put 150 parts of mixture of ice and water in the bucket, add 18.5 parts of 100% cyanuric chlorides, 0 ℃ of making beating 45-60 minute down, slowly drip 26.8 parts of mphenylenediamine disulfonic acid solution of 100% then, in 0-5 ℃ of reaction 2-3 hour to terminal.
Diazonium: contracting in one adds 24 parts of industrial goods hydrochloric acid in the liquid, slowly drips 6.9 parts of sodium nitrite solutions of 100% under 0-5 ℃, finishes, and controlled temperature 0-5 ℃, the little blue colour response of starch potassium iodide paper was eliminated excessive nitrous acid with thionamic acid after 2 hours.
Coupling: 34.1 parts of 2R acid 100% are added in the diazonium salts, and it is 2-7 that the soda ash liquid with 15% is regulated PH, and controlled temperature is 0-10 ℃ simultaneously, reacts that to disappear to diazonium salt be terminal point.
Two contract: 28.1 parts with right-(beta-hydroxyethyl sulfuryl) sulfate ester aniline 100% join in the coupling solution, and to regulate PH with 15% soda ash liquid be 5.5-6.5, be warming up to 40-45 ℃ then, react 4-5 hour to terminal, two things that contract of reaching home are reduced to normal temperature, the muriate that adds 10-20% is then saltoutd, suction filtration, filter cake dry formula (2) dyestuff.
Embodiment two: change the 2R acid in the example 1 into γ acid, other condition same cases down formula (3) structure dyestuff.
Embodiment one gained dyestuff and and embodiment two gained dyestuffs can dye separately, also can be with it by 50: 50 mixed colorant match.

Claims (2)

1. the red reactive dyes of a high light-fast, its structure is as follows:
Figure S2007103024830C00011
A1 is C1
B1 is
Figure S2007103024830C00012
Or
Figure S2007103024830C00013
Figure S2007103024830C00014
A2 is C1
B2 is
Figure S2007103024830C00015
M is 1 or 2
Figure S2007103024830C00021
A3 is C1
B3 is
Figure S2007103024830C00022
Or
Figure S2007103024830C00023
N is 1 or 2
B1 for not isoplastic dyestuff (1) mixes colorant match, is perhaps mixed colorant match with dyestuff (2) with dyestuff (3).
2. the red reactive dyes preparation method of a high light-fast is: cyanuric chloride and mphenylenediamine ortho-sulfonic acid, mphenylenediamine disulfonic acid or Ursol D ortho-sulfonic acid one contract, then and contraposition or a bit esterified thing two contract diazotization and 2R acid or γ acid coupling and getting again; Can also contract by cyanuric chloride and contraposition or a bit esterified thing one, contract with mphenylenediamine ortho-sulfonic acid or mphenylenediamine disulfonic acid or Ursol D ortho-sulfonic acid two again, again diazotization and 2R acid or γ acid coupling and getting.
CNA2007103024830A 2007-12-26 2007-12-26 High light-fast red reactive dye and preparation method thereof Pending CN101230203A (en)

Priority Applications (1)

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CNA2007103024830A CN101230203A (en) 2007-12-26 2007-12-26 High light-fast red reactive dye and preparation method thereof

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Application Number Priority Date Filing Date Title
CNA2007103024830A CN101230203A (en) 2007-12-26 2007-12-26 High light-fast red reactive dye and preparation method thereof

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CN101230203A true CN101230203A (en) 2008-07-30

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102181174A (en) * 2011-03-08 2011-09-14 丽源(湖北)科技有限公司 Red active dye mixture and preparation and application thereof
CN102911528A (en) * 2012-10-31 2013-02-06 无锡润新染料有限公司 Sunlight-resistant chlorine-leaching-resistant composite reactive brilliant red dye
CN112679982A (en) * 2020-12-21 2021-04-20 江苏德美科化工有限公司 Multi-active-base red dye with high color fixing rate and high chlorine fastness for printing and preparation method thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102181174A (en) * 2011-03-08 2011-09-14 丽源(湖北)科技有限公司 Red active dye mixture and preparation and application thereof
CN102911528A (en) * 2012-10-31 2013-02-06 无锡润新染料有限公司 Sunlight-resistant chlorine-leaching-resistant composite reactive brilliant red dye
CN112679982A (en) * 2020-12-21 2021-04-20 江苏德美科化工有限公司 Multi-active-base red dye with high color fixing rate and high chlorine fastness for printing and preparation method thereof

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