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    • 1. 发明公开
    • REACTIVE DYE COMPOUNDS
    • 活性染料化合物
    • EP1066346A1
    • 2001-01-10
    • EP99916317.3
    • 1999-04-01
    • THE PROCTER & GAMBLE COMPANY
    • BROCK, Earl, DavidLEWIS, David, MalcolmYOUSAF, Taher, Iqbal
    • C09B62/02C09B62/503C09B62/20C09B62/04
    • C09B62/4401C09B62/02C09B62/20
    • Reactive dye having a Fixation Value (F) on cellulosic substrates of 95 % or greater as measured by the Fixation Value Technical Test Method (at 2:1 standard depth). In addition, the compounds herein have high Exhaustion Values (E), high Efficiency Values (T) and show significant improvements in terms of reducing spent dyestuff in effluent, increasing dye affinity to the substrate, increasing the dye-substrate covalent bonding, increasing the ability to dye substrates at room temperature, decreasing the amount of dye that is removed during the post dyeing 'soaping off process' and therefore simplying the post dyeing 'soaping off process' traditionally associated with dyeing cotton with fibre reactive dyes and reduction of staining of adjacent white fabrics. In addition, the compounds prepared above provide more intense dyeings and require less levels of salt for dyeing cotton substrates.
    • 通过固色值技术测试方法(在2:1标准深度)测量,在纤维素基材上固定值(F)为95%或更高的活性染料。 此外,本文中的化合物具有高耗竭值(E),高效率值(T)并且在减少流出物中的废染料方面显示出显着的改进,增加染料对基底的亲和力,增加染料 - 基底共价键合,增加 在室温下染色底物的能力,减少在染色后“皂洗过程”中被除去的染料的量,并因此简化传统上与用纤维活性染料染色棉花相关联的染色后“皂洗过程”,以及减少 相邻的白色织物。 另外,上面制备的化合物提供更强烈的染色并且需要较少量的盐用于染色棉基质。
    • 2. 发明公开
    • REACTIVE DYE COMPOUNDS
    • 活性染料化合物
    • EP1066345A1
    • 2001-01-10
    • EP99916316.5
    • 1999-04-01
    • THE PROCTER & GAMBLE COMPANY
    • BROCK, Earl, DavidLEWIS, David, MalcolmYOUSAF, Taher, Iqbal
    • C09B62/02C09B62/503
    • C09B62/02C09B62/4401
    • A reactive dye compound comprising: a) at least one chromophore moiety; b) at least one nitrogen-containing heterocycle; c) a linking group to link each chromophore moiety to each nitrogen-containing heterocycle; characterised in that at least one nitrogen-containing heterocycle is substituted with at least one thio-derivative and at least one quaternized nitrogen derivative. The reactive dye compounds of the invention have high Exhaustion Values, high Fixation Values, particularly on cellulosic substrates such as cotton, and show significant improvements in terms of reducing spent dyestuff in effluent, increasing dye affinity to the substrate, increasing the dye-substrate covalent bonding, increasing the ability to dye substrates at room temperature, decreasing the amount of dye that is removed during the post dyeing 'soaping off process' and therefore simplifying the post dyeing 'soaping off process' traditionally associated with dyeing cotton with fibre reactive dyes and reduction of staining of adjacent white fabrics. In addition, the compounds prepared above provide more intense dyeings and require less levels of salt for dyeing cotton substrates.
    • 一种活性染料化合物,其包含:a)至少一个发色团部分; b)至少一个含氮杂环; c)将每个发色团部分连接到每个含氮杂环的连接基团; 其特征在于至少一个含氮杂环被至少一个硫代衍生物和至少一个季铵化氮衍生物取代。 本发明的活性染料化合物具有高排放值,高定影值,特别是在纤维素基质例如棉上,并且在减少流出物中废染料方面显示出显着的改进,增加染料对基质的亲和力,增加染料 - 基质共价 增加在室温下染色基材的能力,减少在染色后“皂洗过程”中除去的染料量,并由此简化传统上与用纤维活性染料染色棉相关的染色后“皂洗过程”和 减少相邻白色织物的污染。 另外,上面制备的化合物提供更强烈的染色并且需要较少量的盐用于染色棉基质。
    • 4. 发明授权
    • REACTIVE DYE COMPOUNDS
    • 活性染料化合物
    • EP1066343B1
    • 2003-07-16
    • EP99916315.7
    • 1999-04-01
    • THE PROCTER & GAMBLE COMPANY
    • BROCK, Earl, DavidLEWIS, David, MalcolmYOUSAF, Taher, Iqbal
    • C09B62/00
    • C09B62/20
    • Reactive Dye compound having formula (I) wherein: D is a chromophore group; L is a linking moiety; Q is a quaternized nitrogen derivative; X and Y are independently selected from chlorine, bromine, fluorine or hydrogen; A is selected from halogen, preferably chlorine or fluorine; provided that at least one of X and Y is fluorine; A is selected from halogen, preferably chlorine or fluorine; and salts and esters thereof. The reactive dye compounds of the invention have high Exhaustion Values, high Fixation Values, particularly on cellulosic substrates such as cotton, and show significant improvements in terms of reducing spend dyestuff in effluent, increasing dye affinity to the substrate, increasing the dye-substrate covalent bonding, increasing the ability to dye substrates at room temperature, decreasing the amount of dye that is removed during the post dyeing "soaping off process" and therefor simplying the post dyeing "soaping off process" traditionally associated with dyeing cotton with fibre reactive dyes and reduction of staining of adjacent white fabrics. In addition, the compounds prepared above provide more intense dyeings and require less levels of salt for dyeing cotton substrates.
    • 具有式(I)的活性染料化合物,其中:D是发色团; L是连接部分; Q是季铵化的氮衍生物; X和Y独立地选自氯,溴,氟或氢; A选自卤素,优选氯或氟; 条件是X和Y中的至少一个是氟; A选自卤素,优选氯或氟; 及其盐和酯。 本发明的活性染料化合物具有高排放值,高定影值,特别是在纤维素基质例如棉上,并且在减少流出物中花费染料方面显示出显着的改进,增加染料对基质的亲和力,增加染料 - 基质共价 增加在室温下染色基材的能力,减少在染色后“皂洗过程”中除去的染料的量,并因此简化传统上与用纤维活性染料染色棉相关的染色后“皂洗过程”和 减少相邻白色织物的污染。 另外,上面制备的化合物提供更强烈的染色并且需要较少量的盐用于染色棉基质。
    • 5. 发明公开
    • REACTIVE DYE COMPOUNDS
    • 活性染料
    • EP1179033A1
    • 2002-02-13
    • EP00932245.4
    • 2000-05-10
    • The Procter & Gamble Company
    • LEWIS, David, MalcolmHE, Wei, DongYOUSAF, Taher, IqbalGENAIN, Gilles, Yves, Marie, Fernand
    • C09B62/503
    • C09B62/503C09B62/51
    • A reactive dye compound comprising: (a) at least one chromophore moiety; (b) at least one SO2C2H4 group which is attached to the chromophore moiety either directly via the sulphur atom of the SO2C2H4 group or a linking group L; characterised in that at least one SO2C2H4 group is substituted on its terminal carbon atom with at least one Y group wherein Y is -A(CO)R* wherein A is selected from O or S and wherein R' contains at least one terminal nucleophilic group, such as OH, NH2, SH, COOH, N, NHR?1 and NR1R2¿ wherein R?1 and R2¿ may be the same or different and may be selected from C1-C4 alkyl; and salts thereof. Also claimed is a process of manufacture of the compounds herein and products obtainable by the process. The compounds herein have high Exhaustion Values (E), high Fixation Values (F) and high Efficiency Values (T) and show significant improvements in terms of reducing spent dyestuff in effluent, increasing dye affinity to the substrate, increasing the dye-substrate covalent bonding, increasing the ability to dye substrates at room temperature, decreasing the amount of dye that is removed during the post dyeing 'soaping off process' and therefore simplifying the post dyeing 'soaping off process' traditionally associated with dyeing cotton with fibre reactive dyes and reduction of staining of adjacent white fabrics. In addition, the compounds prepared above provide more intense dyeings and require less levels of salt for dyeing cotton substrates.
    • 6. 发明公开
    • REACTIVE DYE COMPOUNDS
    • 活性染料
    • EP1066343A1
    • 2001-01-10
    • EP99916315.7
    • 1999-04-01
    • THE PROCTER & GAMBLE COMPANY
    • BROCK, Earl, DavidLEWIS, David, MalcolmYOUSAF, Taher, Iqbal
    • C09B62/00
    • C09B62/20
    • Reactive Dye compound having formula (I) wherein: D is a chromophore group; L is a linking moiety; Q is a quaternized nitrogen derivative; X and Y are independently selected from chlorine, bromine, fluorine or hydrogen; A is selected from halogen, preferably chlorine or fluorine; provided that at least one of X and Y is fluorine; A is selected from halogen, preferably chlorine or fluorine; and salts and esters thereof. The reactive dye compounds of the invention have high Exhaustion Values, high Fixation Values, particularly on cellulosic substrates such as cotton, and show significant improvements in terms of reducing spend dyestuff in effluent, increasing dye affinity to the substrate, increasing the dye-substrate covalent bonding, increasing the ability to dye substrates at room temperature, decreasing the amount of dye that is removed during the post dyeing 'soaping off process' and therefor simplying the post dyeing 'soaping off process' traditionally associated with dyeing cotton with fibre reactive dyes and reduction of staining of adjacent white fabrics. In addition, the compounds prepared above provide more intense dyeings and require less levels of salt for dyeing cotton substrates.