Reactive orchil component and uses thereof

A reactive dye and composition technology, applied in the field of red dye composition for discharge dyeing, to achieve the effect of excellent dyeing depth

Inactive Publication Date: 2008-06-11
ETHICAL INT WAREHOUSING TRADING SHANGHAI
View PDF4 Cites 10 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0002] So far, regarding the dyeing of fabrics, it is still impossible to obtain highly dyed deep red dyes from a single reactive dye

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Reactive orchil component and uses thereof
  • Reactive orchil component and uses thereof
  • Reactive orchil component and uses thereof

Examples

Experimental program
Comparison scheme
Effect test

preparation example 1

[0060] Take 36.1 parts of 1-aminobenzene-2-sulfonic acid-4-β-sulfonic acid (1-aminobenzene-2-sulfonicacid-4-β-sulfatoethylsulfone) dissolved in 1000 parts of ice water, add 24 parts 32% hydrochloric acid (HCl) aqueous solution was fully stirred, then 7.0 parts of sodium nitrite (sodium nitrite) aqueous solution was added, and the stirring was continued at a temperature of 0-5° C. until the diazotization was completed. Then, 23.9 parts of 2-amino-5-hydroxynaphthalene-7-sulfonic acid were added to the reaction liquid, and the reaction liquid mixture was stirred until the coupling reaction was completed. Finally, add sodium chloride (NaCl) for salting out, and take out by filtration to obtain the compound of the following formula (I-1).

[0061]

[0062] Then take 32.5 parts of 1-aminobenzene-2-methoxy-5-methyl-4-β-sulfate radical ethanesulfonyl (1-aminobenzene-2-methoxy-5-methyl-4-β-sulfatoethylsulfone) Dissolve and disperse in 1000 parts of ice water, add 24 parts of 32% hy...

preparation example 2

[0065] Take 36.1 parts of 1-aminobenzene-2-sulfonicacid-4-β-sulfato-ethylsulfone, dissolve and disperse in 1000 parts of ice water, add 24 parts of 32% hydrochloric acid aqueous solution and stir fully, then add 7.0 parts of sodium nitrite aqueous solution, and then Stirring was continued at 0-5°C until the diazotization was complete. Then, 23.9 parts of 2-amino-5-hydroxynaphthalene-7-sulfonic acid were added to the reaction liquid, and the reaction liquid mixture was stirred until the coupling reaction was completed. Finally, sodium chloride is added for salting out, and the mixture is taken out by filtration to obtain the compound of the following formula (I-2).

[0066]

[0067] Take 34.1 parts of 1-aminobenzene-2,5-dimethoxy-4-β-sulfate ethylsulfonyl (1-aminobenzene-2,5-dimethoxy-4-β-sulfatoethylsulfone) dissolved in 1000 parts In ice water, add 24 parts of 32% hydrochloric acid aqueous solution and stir thoroughly, then add 7.0 parts of sodium nitrite aqueous solution...

preparation example 3

[0070] Take 28.1 parts of 1-aminobenzene-4-β-sulfatoethylsulfonyl (1-aminobenzene-4-β-sulfatoethylsulfone) dissolved in 1000 parts of ice water, add 24 parts of 32% hydrochloric acid aqueous solution and stir thoroughly, Then add 7.0 parts of sodium nitrite aqueous solution, and then keep stirring at a temperature of 0-5° C. until the diazotization is completed. Then, 23.9 parts of 2-amino-5-hydroxynaphthalene-7-sulfonic acid were added to the reaction liquid, and the reaction liquid mixture was stirred until the coupling reaction was completed. Finally, sodium chloride is added for salting out, and the mixture is taken out by filtration to obtain the compound of the following formula (I-3).

[0071]

[0072] Take 34.1 parts of 1-aminobenzene-2, 5-dimethoxy-4-β-sulfato-ethylsulfone, dissolve and disperse in 1000 parts of ice water, add 24 parts of 32% hydrochloric acid aqueous solution and stir fully, then add 7.0 parts of sodium nitrite aqueous solution, and then Stirring...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention provides reactive red dye composition. The composition comprises of at least one of azo reactive dyes selected as the formula (I) illustrated and with the content being of 3 to 97 weight percentage, wherein, the definitions of W, D1 and the D2 are shown in the instruction book; at least one of azo reactive dyes selected as the formula (II) illustrated and with the content being of 97 to 3 weight percentage, wherein the definitions of R, X, Z, D3 and the D4 are shown in the instruction book. The reactive red dye composition of the invention is suitable for the cellulose fiber, and not only can obtain good levelness and deep dyeing effect, but also has excellent white discharging effect.

Description

technical field [0001] The invention relates to a reactive red dye composition, especially a red dye composition suitable for discharge dyeing. Background technique [0002] So far, regarding the dyeing of fabrics, it is still impossible to obtain highly dyed deep red dyes from a single reactive dye. In order to obtain high-dyed crimson dyeing effect, it must be obtained by color mixing method. [0003] Usually, to obtain a red reactive dye composition with high dyeing depth, a reactive red dye is the main body, such as the reactive red dye of the following formula (1), and then combined with orange, yellow or other colored reactive dyes , mixed to obtain a dark red reactive dye composition. [0004] [0005] Among them, the mainland patents CN1524904, CN1730565, CN1730566, the World Patent Organization WO2000006652, WO2006024639 and the US patents US2005034252, US2005034253, etc. have all disclosed similar color mixing dye technologies. Contents of the invention [...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): C09B67/24C09B67/36D06P1/38
CPCC09B67/005C09B67/0059
Inventor 赖宝昆黄惠卿许呈祥曾雅琦
Owner ETHICAL INT WAREHOUSING TRADING SHANGHAI
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap