DE2638542A1 - Wasserloesliches, in nicht polarem loesungsmittel loesliches, ausblutendes faerbemittel - Google Patents
Wasserloesliches, in nicht polarem loesungsmittel loesliches, ausblutendes faerbemittelInfo
- Publication number
- DE2638542A1 DE2638542A1 DE19762638542 DE2638542A DE2638542A1 DE 2638542 A1 DE2638542 A1 DE 2638542A1 DE 19762638542 DE19762638542 DE 19762638542 DE 2638542 A DE2638542 A DE 2638542A DE 2638542 A1 DE2638542 A1 DE 2638542A1
- Authority
- DE
- Germany
- Prior art keywords
- dye
- colorant
- units
- ethylene oxide
- mol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 239000003086 colorant Substances 0.000 title claims description 31
- 239000002798 polar solvent Substances 0.000 title 1
- 239000000975 dye Substances 0.000 claims description 21
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 17
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 16
- 229920000642 polymer Polymers 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 239000012454 non-polar solvent Substances 0.000 claims description 5
- 239000000987 azo dye Substances 0.000 claims description 3
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 3
- 239000001003 triarylmethane dye Substances 0.000 claims description 3
- CREXVNNSNOKDHW-UHFFFAOYSA-N azaniumylideneazanide Chemical group N[N] CREXVNNSNOKDHW-UHFFFAOYSA-N 0.000 claims 2
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 claims 1
- 238000002360 preparation method Methods 0.000 description 17
- 150000001875 compounds Chemical class 0.000 description 14
- 239000012954 diazonium Substances 0.000 description 10
- 150000001989 diazonium salts Chemical class 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- -1 polyoxyethylene chains Polymers 0.000 description 9
- 238000000034 method Methods 0.000 description 8
- 239000004753 textile Substances 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 7
- 239000002253 acid Substances 0.000 description 5
- 239000000835 fiber Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- SHHKMWMIKILKQW-UHFFFAOYSA-N 2-formylbenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1C=O SHHKMWMIKILKQW-UHFFFAOYSA-N 0.000 description 4
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 4
- 239000004744 fabric Substances 0.000 description 4
- 229950011008 tetrachloroethylene Drugs 0.000 description 4
- 239000001060 yellow colorant Substances 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000000740 bleeding effect Effects 0.000 description 3
- 239000001045 blue dye Substances 0.000 description 3
- SQYUJKVKVFILNB-UHFFFAOYSA-N methyl 2-amino-4-[(2,5-dichlorophenyl)carbamoyl]benzoate Chemical compound C1=C(N)C(C(=O)OC)=CC=C1C(=O)NC1=CC(Cl)=CC=C1Cl SQYUJKVKVFILNB-UHFFFAOYSA-N 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical group C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 2
- 150000004982 aromatic amines Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 238000005108 dry cleaning Methods 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000001061 orange colorant Substances 0.000 description 2
- 125000005702 oxyalkylene group Chemical group 0.000 description 2
- 125000006353 oxyethylene group Chemical group 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical group C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical group N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 1
- UNVXHJAPRFOGAG-UHFFFAOYSA-N 3-ethyl-n,n-dihydroxy-2,5-dimethoxyaniline Chemical compound CCC1=CC(OC)=CC(N(O)O)=C1OC UNVXHJAPRFOGAG-UHFFFAOYSA-N 0.000 description 1
- QZHXKQKKEBXYRG-UHFFFAOYSA-N 4-n-(4-aminophenyl)benzene-1,4-diamine Chemical group C1=CC(N)=CC=C1NC1=CC=C(N)C=C1 QZHXKQKKEBXYRG-UHFFFAOYSA-N 0.000 description 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical group C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical group C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 239000001000 anthraquinone dye Chemical group 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 150000003934 aromatic aldehydes Chemical class 0.000 description 1
- UNTBPXHCXVWYOI-UHFFFAOYSA-O azanium;oxido(dioxo)vanadium Chemical compound [NH4+].[O-][V](=O)=O UNTBPXHCXVWYOI-UHFFFAOYSA-O 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000000038 blue colorant Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical group C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 239000000040 green colorant Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Chemical group COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000000018 nitroso group Chemical group N(=O)* 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 150000003142 primary aromatic amines Chemical class 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- ALDITMKAAPLVJK-UHFFFAOYSA-N prop-1-ene;hydrate Chemical compound O.CC=C ALDITMKAAPLVJK-UHFFFAOYSA-N 0.000 description 1
- 239000001062 red colorant Substances 0.000 description 1
- 239000001044 red dye Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000001043 yellow dye Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B69/00—Dyes not provided for by a single group of this subclass
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2618—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing nitrogen
- C08G65/2621—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing nitrogen containing amine groups
- C08G65/2627—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing nitrogen containing amine groups containing aromatic or arylaliphatic amine groups
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
- D06P5/13—Fugitive dyeing or stripping dyes
- D06P5/138—Fugitive dyeing or stripping dyes fugitive dyeing
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Coloring (AREA)
- Polyethers (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US60936975A | 1975-09-02 | 1975-09-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2638542A1 true DE2638542A1 (de) | 1977-03-03 |
Family
ID=24440509
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19762638542 Withdrawn DE2638542A1 (de) | 1975-09-02 | 1976-08-26 | Wasserloesliches, in nicht polarem loesungsmittel loesliches, ausblutendes faerbemittel |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US4113721A (https=) |
| JP (1) | JPS5933622B2 (https=) |
| BE (1) | BE845749A (https=) |
| CA (1) | CA1081906A (https=) |
| CH (1) | CH616716A5 (https=) |
| DE (1) | DE2638542A1 (https=) |
| DK (1) | DK147395C (https=) |
| FR (1) | FR2322908A1 (https=) |
| GB (1) | GB1497017A (https=) |
| IT (1) | IT1074488B (https=) |
| MX (1) | MX145150A (https=) |
| NL (1) | NL7609737A (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008100445A3 (en) * | 2007-02-09 | 2009-05-07 | Milliken & Co | Unsubstituted and polymeric leuco colorants for coloring consumer products |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4400320A (en) * | 1981-07-13 | 1983-08-23 | Milliken Research Corporation | Alkyleneoxy fugitive tints containing a 2-amino, 6-methoxy benzathiazole group and process for preparing such fugitive tints |
| US4507407A (en) * | 1984-06-25 | 1985-03-26 | Milliken Research Corporation | Process for in situ coloration of thermosetting resins |
| US4601725A (en) * | 1984-08-27 | 1986-07-22 | Milliken Research Corporation | Thiophene based fugitive colorants |
| US4977281A (en) * | 1987-12-21 | 1990-12-11 | Milliken Research Corporation | Polyoxyalkylene amino alcohols and polyoxyalkylene amino 1,3-dioxanes and 1,3-dioxolanes |
| US4985546A (en) * | 1987-12-21 | 1991-01-15 | Milliken Research Corporation | Polyoxylalkylene amino diol substituted colorants |
| US4871371A (en) * | 1988-10-24 | 1989-10-03 | Milliken Research Corporation | Tint compositions useful for providing coloration to aqueous and non-aqueous liquids |
| US4946509A (en) * | 1989-05-23 | 1990-08-07 | Sun Chemical Corporation | Diarylide pigment compositions |
| US4946508A (en) * | 1989-05-23 | 1990-08-07 | Sun Chemical Corporation | Disazo pyrazolone pigment compositions |
| US5052380A (en) * | 1989-07-07 | 1991-10-01 | Minnesota Mining And Manufacturing Company | Colored orthopedic resins and orthopedic casting materials incorporating same |
| US5591833A (en) * | 1990-06-28 | 1997-01-07 | Milliken Research Corporation | Colorants and intermediates therefor having branched poly(oxyalkylene)moieties, and their manufacture |
| US5108460A (en) * | 1990-10-19 | 1992-04-28 | Milliken Research Corporation | Azo dimer and trimer fugitive tints |
| CA2050019A1 (en) * | 1991-08-27 | 1993-02-28 | John Bery Hines | Colorants and intermediates therefor having branched poly(oxyalkylene) moieties, and their manufacture |
| US6124036A (en) * | 1993-08-06 | 2000-09-26 | Milliken & Company | Aqueous colorant composition in water-soluble package |
| CA2134156A1 (en) * | 1993-11-22 | 1995-05-23 | Thomas P. Klun | Coatable compositions, abrasive articles made therefrom, and methods of making and using same |
| US5532346A (en) * | 1994-10-21 | 1996-07-02 | Milliken Research Corporation | Hydroxynaphthalenecarboxylic acid compounds and azo colorants made therefrom |
| US5864002A (en) * | 1996-10-18 | 1999-01-26 | Milliken Research Corporation | Process for coloring polymer resins and products thereof |
| US6369128B1 (en) | 1997-02-07 | 2002-04-09 | Milliken & Company | Aqueous ink composition |
| US6069276A (en) * | 1999-03-05 | 2000-05-30 | Milliken & Company | Oxyalkylene-substituted m-amidoaniline intermediate |
| AR049538A1 (es) | 2004-06-29 | 2006-08-09 | Procter & Gamble | Composiciones de detergentes para lavanderia con colorante entonador eficiente |
| US7097669B2 (en) * | 2004-11-18 | 2006-08-29 | Milliken & Company | Colorant compositions |
| US7342113B2 (en) * | 2004-11-18 | 2008-03-11 | Milliken & Company | Colorant compositions |
| US7786203B2 (en) * | 2005-09-16 | 2010-08-31 | Milliken & Company | Polymer compositions comprising nucleating or clarifying agents and articles made using such compositions |
| US7572325B2 (en) * | 2005-11-30 | 2009-08-11 | Xerox Corporation | Ink carriers, phase change inks including same and methods for making same |
| US7758268B2 (en) * | 2005-12-20 | 2010-07-20 | Xerox Corporation | Hand held photochromic marking implement |
| PL1975226T3 (pl) * | 2007-03-20 | 2013-07-31 | Procter & Gamble | Płynna kompozycja do obróbki |
| CN102906239B (zh) | 2010-05-18 | 2015-09-09 | 美利肯公司 | 荧光增白剂及含有其的组合物 |
| US8664371B2 (en) | 2010-07-02 | 2014-03-04 | Spectra Colors Corp. | Rinsable dyes and methods for their preparation |
| US8653247B2 (en) | 2010-07-02 | 2014-02-18 | Spectra Colors Corp. | Rinsable dyes and methods for their preparation |
| WO2013026451A1 (en) | 2011-08-24 | 2013-02-28 | Coloplast A/S | Polymers comprising photoinitiator moieties and dye moieties |
| EP2757118A1 (en) | 2013-01-17 | 2014-07-23 | Allnex Belgium, S.A. | Radiation curable aqueous compositions with reversible drying. |
| EP3097173B1 (en) * | 2014-01-22 | 2020-12-23 | The Procter and Gamble Company | Fabric treatment composition |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1310078A (https=) * | 1963-03-04 | |||
| GB421117A (en) * | 1933-03-04 | 1934-12-06 | Ig Farbenindustrie Ag | Improvements in the manufacture and production of organic dyestuffs |
| US3022335A (en) * | 1955-03-30 | 1962-02-20 | Wyandotte Chemicals Corp | Surface active polyoxyalkylene compounds having a plurality of heteric polyoxypropylene-polyoxyethylene chains |
| US3101374A (en) * | 1958-08-19 | 1963-08-20 | Wyandotte Chemicals Corp | Polyoxyalkylene surface active agents having heteric polyoxyethylene solubilizing chains |
| NL129418C (https=) * | 1959-07-08 | |||
| US3157633A (en) * | 1960-11-28 | 1964-11-17 | Deering Milliken Res Corp | Polyethyleneoxy fugitive tints |
| US3337525A (en) * | 1964-06-05 | 1967-08-22 | Deering Milliken Res Corp | (hydroxyethyl polyethyleneoxyamino)-phenylazo naphthalen-1, 8-diols |
| US3449319A (en) * | 1965-09-01 | 1969-06-10 | Deering Milliken Res Corp | Water soluble polymeric surfactant azo fugitive tints |
| CH584279A5 (https=) * | 1973-09-27 | 1977-01-31 | Ciba Geigy Ag |
-
1976
- 1976-08-20 CA CA259,534A patent/CA1081906A/en not_active Expired
- 1976-08-26 DE DE19762638542 patent/DE2638542A1/de not_active Withdrawn
- 1976-08-26 GB GB35462/76A patent/GB1497017A/en not_active Expired
- 1976-08-30 MX MX166097A patent/MX145150A/es unknown
- 1976-08-31 FR FR7626287A patent/FR2322908A1/fr active Granted
- 1976-09-01 DK DK395276A patent/DK147395C/da not_active IP Right Cessation
- 1976-09-01 BE BE170271A patent/BE845749A/xx not_active IP Right Cessation
- 1976-09-01 CH CH1109076A patent/CH616716A5/fr not_active IP Right Cessation
- 1976-09-01 IT IT51097/76A patent/IT1074488B/it active
- 1976-09-01 NL NL7609737A patent/NL7609737A/xx not_active Application Discontinuation
- 1976-09-02 JP JP51104365A patent/JPS5933622B2/ja not_active Expired
-
1977
- 1977-07-13 US US05/815,122 patent/US4113721A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008100445A3 (en) * | 2007-02-09 | 2009-05-07 | Milliken & Co | Unsubstituted and polymeric leuco colorants for coloring consumer products |
Also Published As
| Publication number | Publication date |
|---|---|
| IT1074488B (it) | 1985-04-20 |
| DK395276A (da) | 1977-03-03 |
| NL7609737A (nl) | 1977-03-04 |
| FR2322908A1 (fr) | 1977-04-01 |
| DK147395B (da) | 1984-07-16 |
| DK147395C (da) | 1985-02-04 |
| FR2322908B1 (https=) | 1981-03-20 |
| CH616716A5 (https=) | 1980-04-15 |
| JPS5230821A (en) | 1977-03-08 |
| GB1497017A (en) | 1978-01-05 |
| CA1081906A (en) | 1980-07-22 |
| MX145150A (es) | 1982-01-12 |
| JPS5933622B2 (ja) | 1984-08-16 |
| BE845749A (fr) | 1976-12-31 |
| US4113721A (en) | 1978-09-12 |
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