| Patent Number |
Title Of Patent |
Date Issued |
| 6706801 |
Aqueous reactive putty (I) |
March 16, 2004 |
| The invention relates to aqueous reactive 2-component binder combinations for aqueous reactive filler compositions, processes for the preparation of aqueous reactive filler compositions based on aqueous reactive 2-component binder combinations and the use of such filler compositions. |
| 6562894 |
Aqueous reactive putties (II) |
May 13, 2003 |
| The invention relates to aqueous reactive 2-component binder combinations for aqueous reactive filler compositions, processes for the preparation of aqueous reactive filler compositions based on aqueous reactive 2-component binder combinations and the use of such filler compositions. |
| 5762652 |
Process for dyeing or printing fibre materials containing hydroxyl groups |
June 9, 1998 |
| Process for dyeing or printing fiber materials containing hydroxyl groups, characterized in that at least one blue-dyeing dyestuff of the formula ##STR1## wherein the substituents have the meaning given in the description, is used together with at least one yellow-dyeing and/or at le |
| 5665124 |
Process for dyeing and printing materials containing hydroxyl and/or carboxamide groups |
September 9, 1997 |
| Dyeings having improved properties are obtained with a dyestuff of the following formula ##STR1## wherein the substituents have the meaning given in the description. |
| 5653773 |
Process for dyeing or printing fibre materials containing hydroxyl groups |
August 5, 1997 |
| Process for dyeing or printing fibre materials containing hydroxyl groups, characterized in that at least one blue-dyeing dyestuff of the formula ##STR1## wherein the substituents have the meaning given in the description, is used together with at least one yellow-dyeing and/or at l |
| 5625042 |
Diazo reactive dyestuffs, their preparations and use |
April 29, 1997 |
| Novel reactive dyestuffs of the general formula ##STR1## in which A represents CH.dbd.CH, or CH.sub.2 --CH.sub.2 Z, in which Z denotes a substituent which can be split off under dyeing conditions,and in which the other groups have the meaning given in the description, show improved a |
| 5623061 |
Benzene or naphthalene azo dyes containing SO.sub.2 X and triazinyl fiber reactive groups, use t |
April 22, 1997 |
| The invention relates to azo reactive dyes of the formula ##STR1## in which D denotes the radical of a diazo component of the benzene or naphthalene series,X denotes CH.dbd.CH.sub.2 or CH.sub.2 CH.sub.2 --Z, in which Z denotes a radical which can be eliminated under dyeing conditions |
| 5569747 |
Reactive disazo dyestuffs which contain two heterocyclic reactive groups |
October 29, 1996 |
| Azo class reactive dyestuffs have been found which have the general formula (1) ##STR1## and in which Z.sup.1 and Z.sup.2 represent a reactive group from the pyrimidine series, X represents SR.sup.1, OR.sup.2 or NR.sup.3 R.sup.4, and the remaining substituents have the meanings g |
| 5456728 |
Reactive dyestuff mixture having improved properties in combination |
October 10, 1995 |
| An improved reactive dyestuff mixture comprises at least one monochlorotriazine dyestuff 1 and at least one monofluorotriazine dyestuff 2 and/or fluorochloropyrimidine dyestuff 3, and if appropriate additional dyestuffs having the formulae given in the description. |
| 5423888 |
Reactive dyestuff green mixture having reduced dichroism |
June 13, 1995 |
| A reactive dyestuff mixture contains at least one vinylsulphonylphthalocyanine dyestuff, at least one Ni fluoro-chloropyrimidenyl phthalocyanine dyestuff and/or one Ni chlorotriazinyl-phthalocyanine dyestuff. |
| 5399182 |
Reactive dyestuff red mixture |
March 21, 1995 |
| Improved reactive dyestuff red mixtures comprise in each case at least one component of the formula 1 ##STR1## and one component of the formula 2 ##STR2## wherein the substituents have the meaning given in the description. |
| 5393307 |
Reactive dyestuff mixture |
February 28, 1995 |
| A reactive dyestuff mixture showing improved compatibility contains at least one vinylsulphonyltriazine dyestuff 1, at least one monofluorotriazine dyestuff 2 or fluorochloropyrimidine dyestuff 3 together with, if desired, additional dyestuffs. |
| 5364416 |
Reactive dyestuff mixtures |
November 15, 1994 |
| Improved reactive dyestuff mixtures comprise a reactive dyestuff of the formula (I) ##STR1## and a chlorotriazine dyestuff of the formula ##STR2## wherein the substituents have the meaning given in the description. |
| 5356444 |
Phthalocyanine reactive dyestuff mixture |
October 18, 1994 |
| A phthalocyanine reactive dyestuff mixture having an improved dyeing levelness and combination properties comprises at least one phthalocyanine vinylsulphonyl reactive dyestuff 1, at least one phthalocyanine fluorochloropyrimidinyl reactive dyestuff 2 and/or a phthalocyanine monochlo |
| 5304221 |
Reactive dyestuff mixtures |
April 19, 1994 |
| New dyestuff mixtures contain in each case at least one fluoropyrimidine dyestuff of the general formula (I) ##STR1## and a vinylsulfonyl dyestuff of the formula (II) ##STR2## in which the substituents have the meaning given in the description. |
| 5279622 |
Solid dyestuff preparations having improved water solubility |
January 18, 1994 |
| Solid dyestuff preparations of reactive phthalocyanine dyestuffs of the formula ##STR1## in which the substituents have the meaning given in the description, have improved solubility in water if they contain 5 to 15% by weight of an acid-binding agent. |
| 5057609 |
Triphendioxazine dyestuffs |
October 15, 1991 |
| Dyestuffs of the formula ##STR1## in which the substituents have the meanings given in the description are suitable for the dyeing and printing of hydroxy-containing and amido-containing materials. They produce blue dyeings having high color density and high light fastness and we |
| 4778603 |
Process for the preparation of a concentrated aqueous reactive dyestuff solution |
October 18, 1988 |
| Ultrafiltered solutions of the dyestuff of the formula ##STR1## (Me=cation) such as is obtained directly on synthesis, are distinguished by an increased tinctorial strength in pad-steam dyeing of cellulose fibres. |
