EP0376893A2 - Liquid laundry detergent compositions containing optical brighteners - Google Patents
Liquid laundry detergent compositions containing optical brighteners Download PDFInfo
- Publication number
- EP0376893A2 EP0376893A2 EP89810985A EP89810985A EP0376893A2 EP 0376893 A2 EP0376893 A2 EP 0376893A2 EP 89810985 A EP89810985 A EP 89810985A EP 89810985 A EP89810985 A EP 89810985A EP 0376893 A2 EP0376893 A2 EP 0376893A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- laundry detergent
- liquid laundry
- detergent composition
- formula
- composition according
- 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- Withdrawn
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/40—Dyes ; Pigments
- C11D3/42—Brightening agents ; Blueing agents
Definitions
- the invention relates to liquid laundry detergent compositions containing optical brighteners.
- optical brighteners in laundry detergent compositions has been known for a long time.
- optical brighteners with poor water solubility are used as dispersions because such products should have enough substantivity, which means that their affinity to the fibres of the substrate that is to be washed, should be high enough in order not to be washed out immediately.
- the use of such products has the disadvantage that the detergent compositions have a poor storage stability, that is to say that the optical brightener will precipitate. If, on the other hand, optical brighteners were to be used which are more soluble in water, these products would have an insufficient substantivity to the fibres of the substrate to be washed.
- both groups R are the same and both groups X are the same and the alkyl and alkylene groups have the same number of carbon atoms i.e. compounds of formulae I and II are preferably symmetrical. More preferably, in compounds of formula 1, X is other than hydroxy or R1 is hydrogen. Especially preferred compounds have the structure of formulae III, IV, V, VI and/or VII. Most preferred compound is the one of formula III.
- optical brighteners according to the invention are used in powder form or as solutions in water. Such solutions have a content of 18 to 75% by weight of active substance and preferably also contain hydrotropic substances.
- active substances are well known and can be produced according to conventional processes.
- liquid laundry detergent compositions according to the invention contain the usual components of such compositions.
- such components include anionic as well as non-ionic surfactants, builders, alkali, hydrotropic agents, buffers, enzymes and the like will be contained. It is also possible to include cationic softeners which will not precipitate.
- Typical detergent compositions contain from 0.05 to 0.15% by weight of optical brighteners (as 100% active substance), from 5 to 30%, preferably from 10 to 25% by weight of fatty acids, from 2 to 20%, preferably from 5 to 15% by weight of a further anionic surfactant, from 0.5 to 12%, preferably from 1.5 to 8% by weight of a non-ionic surfactant, to give in total from 20 to 50%, preferably from 30 to 50% by weight of surfactants and from 5 to 15% by weight of builders.
- the amount of alkali should be sufficient to neutralize all acids present and to reach a pH value suitable for washing.
- the fatty acids which are used as anionic surfactants are preferably saturated and unsaturated C5 ⁇ 22 carboxylic acids, more preferably C12 ⁇ 18.
- the fatty acids for example coco fatty acid or oleic acid are added as such and converted to the salt form by addition of alkali e.g. NaOH, KOH or an organic base e.g. triethanolamine.
- anionic surfactants which can be present may be any of the following conventional types:
- a preferred class of surfactants which are only weakly anionic are of the formula IX R-O-(CH2CH2O (A-COOH) x IX in which R is the residue of a C8 ⁇ 22 fatty alcohol or of an alkylphenol having 10-24 C atoms; A is a methylene or ethylene group; m is a number from 1-20; and x is an average value from 0.1 to 1.
- the most preferred component (B) is a compound of formula IX obtained by reacting a synthetic lauryl alcohol (C12 ⁇ 15) with 4-5 moles ethylene oxide and subsequently with 0.8 mole chloracetic acid.
- the compounds are normally used in the form of their alkali metal salts, particularly sodium salts.
- Nonionic surfactants which may be present include ethylene oxide (EO) / propylene oxide (PO) block copolymers (Pluronics), and the addition products of EO or PO, preferably EO, to fatty alcohols, fatty amines, fatty acids, fatty acid alkanolamides and alkylphenols. Such non-ionic surfactants are conventional and commercially available.
- Hydrotropic compounds which may be present include for example urea, dicyandiamide and its derivatives, alcohols, water-soluble glycols, glycol ethers and glycol esters and C1 ⁇ 4 alkylbenzenesulphonates, provided that the compounds display no cloud point in distilled water up to 100°. They act so as to prevent phase separation, that is to stabilize the liquid composition.
- Sequestering agents include citric acid, nitrilotriacetic acid and other complex formers. Buffers may be used to stabilise the pH of the wash liquor in the neutral or alkali region. Buffer substances include sodium bicarbonate, sodium carbonate and sodium silicate.
- cationic softeners e.g., products of acylation and quaternization of a polyalkylene polyamine of the formula X in which each R1, independently, is C12 ⁇ 18 alkyl or C12 ⁇ 18 alkenyl; each n, independently, is 2 or 3; R2 is C1 ⁇ 4 alkyl, C1 ⁇ 4 hydroxyalkyl, or C1 ⁇ 4 hydroxyalkyl etherified with 1-10 ethylene oxide groups; R3 is C1 ⁇ 4 alkyl or benzyl; and X ⁇ is a halide, methylsulphate or ethylsulphate anion.
- cationic softeners e.g., products of acylation and quaternization of a polyalkylene polyamine of the formula X in which each R1, independently, is C12 ⁇ 18 alkyl or C12 ⁇ 18 alkenyl; each n, independently, is 2 or 3; R2 is C1 ⁇ 4 alkyl, C1 ⁇ 4 hydroxyalkyl,
- the liquid detergent compositions of the invention are primarily useful as domestic laundry detergents. Not only do they display good washing power, they also produce a soft handle on laundered cotton goods. Being phosphate-free, they are ecologically acceptable.
- the liquid compositions of the invention are stable and do not separate into two phases, nor do the optical brighteners crystallize and precipitate on storage.
- the carboxymethylated ethylene oxide adduct of the formula C12 ⁇ 15O(CH2CH2O) 4,5 - (CH2COONa) 0,7 as a 50% paste in water, the non-ionic surfactant of the formula as a 99% paste in water, the softener of the formula in which R x 85% oleic acid and 15% stearic acid residue, as a 90% solution in water, polyacrylic acid A with MW 100.00 as a solution of 29% of the semi-neutralized acid (sodium salt), polyacrylic acid B with MW 4500 as a solution of 49% are used as well as the optical brighteners with the given formulas in the following compositions: Formula III as an aqueous solution that contains 28% active substance or as a powder with 89% active substance Formula IV as an aqueous solution that contains 20% active substance Formula V as an aqueous solution that contains 23% active substance or as a powder with 50% active substance Formula VII as an aqueous
- Example 1 is a so-called fabric softener
- Example 2 is a liquid laundry detergent for industrial use
- Example 3 is a complete laundry detergent for domestic use
- Example 4 is a liquid laundry detergent with fabric softener for domestic use
- Examples 5 and 6 are liquid laundry detergents for domestic use
- Example 7 is a concentrated complete laundry detergent for domestic use.
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
Abstract
Description
- The invention relates to liquid laundry detergent compositions containing optical brighteners.
- The use of optical brighteners in laundry detergent compositions has been known for a long time. In liquid compositions in general, optical brighteners with poor water solubility are used as dispersions because such products should have enough substantivity, which means that their affinity to the fibres of the substrate that is to be washed, should be high enough in order not to be washed out immediately. The use of such products, however, has the disadvantage that the detergent compositions have a poor storage stability, that is to say that the optical brightener will precipitate. If, on the other hand, optical brighteners were to be used which are more soluble in water, these products would have an insufficient substantivity to the fibres of the substrate to be washed.
- It has been found that when using optical brighteners of a specific chemical structure which are water soluble, laundry detergent compositions with sufficient storage stability can be obtained.
- Similar optical brighteners have been used in liquid detergent compositions as described in US Patent 4,233,167 and in European patent published application no. 106407. The problem to solve in these known detergent compositions was to find optical brighteners which would not counteract the effect of cationic softeners and would not provoke these softeners to be deposited on fabrics as a yellow film (USP 4,233,167) or optical brighteners which would not form insoluble complexes with the cationic surfactants contained in detergent compositions. The preferred compounds mentioned in these patent specifications do not have the desired substantivity.
- The invention provides a liquid laundry detergent composition containing one or more optical brighteners of formula I
in which both groups R, independently, are hydrogen, halogen, C₁₋₂ alkyl, C₁₋₂ alkoxy, hydroxy or sulfonic acid groups,
each alkylene, independently, is an alkylene group with 2 or 3 carbon atoms,
each X, independently, is halogen, cyano, carboxamido, C₁₋₂ alkoxy or hydroxy,
and R1 is hydrogen or Alkylene -X, with the proviso that if X = hydroxy, R should not be a sulfonic acid group in the para-position,
or containing optical brighteners of formula II
both alkyl groups, independently, have 1 or 2 carbon atoms, and both groups M are hydroxyalkylammonium cations. - Preferably, in formula I and II, both groups R are the same and both groups X are the same and the alkyl and alkylene groups have the same number of carbon atoms i.e. compounds of formulae I and II are preferably symmetrical. More preferably, in compounds of formula 1, X is other than hydroxy or R₁ is hydrogen. Especially preferred compounds have the structure of formulae III, IV, V, VI and/or VII. Most preferred compound is the one of formula III.
- The optical brighteners according to the invention are used in powder form or as solutions in water. Such solutions have a content of 18 to 75% by weight of active substance and preferably also contain hydrotropic substances. The active substances are well known and can be produced according to conventional processes.
- Besides optical brighteners, the liquid laundry detergent compositions according to the invention contain the usual components of such compositions. In general, such components include anionic as well as non-ionic surfactants, builders, alkali, hydrotropic agents, buffers, enzymes and the like will be contained. It is also possible to include cationic softeners which will not precipitate.
- The amounts of the components of such liquid laundry detergent composition are in the usual ranges. Typical detergent compositions contain from 0.05 to 0.15% by weight of optical brighteners (as 100% active substance), from 5 to 30%, preferably from 10 to 25% by weight of fatty acids, from 2 to 20%, preferably from 5 to 15% by weight of a further anionic surfactant, from 0.5 to 12%, preferably from 1.5 to 8% by weight of a non-ionic surfactant, to give in total from 20 to 50%, preferably from 30 to 50% by weight of surfactants and from 5 to 15% by weight of builders. The amount of alkali should be sufficient to neutralize all acids present and to reach a pH value suitable for washing.
- The fatty acids which are used as anionic surfactants are preferably saturated and unsaturated C₅₋₂₂ carboxylic acids, more preferably C₁₂₋₁₈. The fatty acids, for example coco fatty acid or oleic acid are added as such and converted to the salt form by addition of alkali e.g. NaOH, KOH or an organic base e.g. triethanolamine.
- Further anionic surfactants which can be present may be any of the following conventional types:
- a) sulphates and sulphonates of fatty acids, fatty acid esters and fatty acid amides
- b) linear or branched C₅₋₁₈ alkyl sulphates and sulphonates
- c) sulphated ethoxylated compounds, particularly sulphated forms of any non-ionic surfactants which may be present
- d) polycarboxylic acid ester sulphates and
- e) C₅₋₁₈ alkylbenzenesulphonates and C₁₋₄ alkyl and dialkylnaphthalene sulphonates.
- These compounds may be added in acid form and converted to their salt forms by addition of alkali.
- A preferred class of surfactants which are only weakly anionic are of the formula IX
R-O-(CH₂CH₂O(A-COOH)x IX
in which R is the residue of a C₈₋₂₂ fatty alcohol or of an alkylphenol having 10-24 C atoms;
A is a methylene or ethylene group;
m is a number from 1-20;
and x is an average value from 0.1 to 1. - Compounds of formula IX are known or may be prepared by conventional methods from available starting materials. The most preferred component (B) is a compound of formula IX obtained by reacting a synthetic lauryl alcohol (C₁₂₋₁₅) with 4-5 moles ethylene oxide and subsequently with 0.8 mole chloracetic acid. The compounds are normally used in the form of their alkali metal salts, particularly sodium salts.
- Nonionic surfactants which may be present include ethylene oxide (EO) / propylene oxide (PO) block copolymers (Pluronics), and the addition products of EO or PO, preferably EO, to fatty alcohols, fatty amines, fatty acids, fatty acid alkanolamides and alkylphenols. Such non-ionic surfactants are conventional and commercially available.
- Hydrotropic compounds which may be present include for example urea, dicyandiamide and its derivatives, alcohols, water-soluble glycols, glycol ethers and glycol esters and C₁₋₄ alkylbenzenesulphonates, provided that the compounds display no cloud point in distilled water up to 100°. They act so as to prevent phase separation, that is to stabilize the liquid composition.
- Sequestering agents include citric acid, nitrilotriacetic acid and other complex formers. Buffers may be used to stabilise the pH of the wash liquor in the neutral or alkali region. Buffer substances include sodium bicarbonate, sodium carbonate and sodium silicate.
- Further optional components include cationic softeners, e.g., products of acylation and quaternization of a polyalkylene polyamine of the formula X
each n, independently, is 2 or 3;
R₂ is C₁₋₄ alkyl, C₁₋₄ hydroxyalkyl, or C₁₋₄ hydroxyalkyl etherified with 1-10 ethylene oxide groups;
R₃ is C₁₋₄ alkyl or benzyl;
and X⊖ is a halide, methylsulphate or ethylsulphate anion. - By selection of these additional components the washing effect of the liquid detergent can be adjusted for the desired field of use. The liquid detergent compositions of the invention are primarily useful as domestic laundry detergents. Not only do they display good washing power, they also produce a soft handle on laundered cotton goods. Being phosphate-free, they are ecologically acceptable. The liquid compositions of the invention are stable and do not separate into two phases, nor do the optical brighteners crystallize and precipitate on storage.
- In the following examples 1 to 7 (table), the carboxymethylated ethylene oxide adduct of the formula
C₁₂₋₁₅O(CH₂CH₂O)4,5 - (CH₂COONa)0,7
as a 50% paste in water, the non-ionic surfactant of the formula
Formula III as an aqueous solution that contains 28% active substance
or as a powder with 89% active substance
Formula IV as an aqueous solution that contains 20% active substance
Formula V as an aqueous solution that contains 23% active substance
or as a powder with 50% active substance
Formula VII as an aqueous solution that contains 34% active substance
Formula VI as an aqueous solution that contains 33% active substance. - Example 1 is a so-called fabric softener, Example 2 is a liquid laundry detergent for industrial use, Example 3 is a complete laundry detergent for domestic use, Example 4 is a liquid laundry detergent with fabric softener for domestic use, Examples 5 and 6 are liquid laundry detergents for domestic use, and Example 7 is a concentrated complete laundry detergent for domestic use.
Table Percentage by weight Example 1 2 3 4 5 6 7 Component Demineralised water 86.4 65.0 57.8 27.5 31.7 30.5 53.9 sodium xylenesulphonate - 4.5 6.0 - - - 6.5 isopropanol 2.0 - - 12.0 12.0 12.0 - ethylene glycol - 3.0 - - - - - propylene glycol 5.0 - - - - - - dodecylbenzene sulphonic acid - 2.0 6.0 8.0 8.0 8.0 6.0 coco fatty acid - - 6.0 15.0 8.0 12.0 6.0 oleic acid - 2.0 - 5.0 5.0 5.0 - Carboxymethylated ethylene oxide adduct - - - 15.0 20.0 20.0 - non-ionic surfactant - - - - 5.0 - - softener 6.5 - - 5.0 - - - sodium hydroxide - 2.7 - - 1.8 - - potassium hydroxide - - 6.2 - - - 5.1 diethanolamine - - - 11.7 - 8.0 - triethanolamine - - - - 8.0 4.0 - sodium hydrogen carbonate - - 2.5 - - - - sodium silicate (Na₂O:SiO₂)1:2 - 10.0 - - - - 4.5 sodium nitrilotriacetate - 3.0 - - - - 2.0 polyacrylic acid A - - 15.0 - - - 15.0 polyacrylic acid B - 7.5 - - - - - brightener III liquid 0.1 - - - - - - III powder - 0.3 - - - - - IV liquid - - 0.5 - - - - V liquid - - - 0.8 - - - V powder - - - - 0.5 - - VII liquid - - - - - 0.5 - VI liquid - - - - - - 1.0 100.0 100.0 100.0 100.0 100.0 100.0 100.0 pH of the solution 5.5 13.3 9.5 7.5 7.5 7.5 12.5
Claims (10)
in which both groups R, independently, are hydrogen, halogen, C₁₋₂ alkyl, C₁₋₂ alkoxy, hydroxy or sulfonic acid groups,
each alkylene, independently, is an alkylene group with 2 or 3 carbon atoms,
each X, independently, is halogen, cyano, carboxamido, C₁₋₂ alkoxy or hydroxy,
and R₁ is hydrogen or Alkylene -X, with the proviso that if X = hydroxy, R should not be a sulfonic acid group in the para-position,
or containing optical brighteners of formula II in which R is as defined above,
both alkyl groups, independently, have 1 or 2 carbon atoms, and both groups M are hydroxyalkylammonium cations.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19883844341 DE3844341A1 (en) | 1988-12-30 | 1988-12-30 | LIQUID DETERGENT |
DE3844341 | 1988-12-30 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0376893A2 true EP0376893A2 (en) | 1990-07-04 |
EP0376893A3 EP0376893A3 (en) | 1991-08-07 |
Family
ID=6370541
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19890810985 Withdrawn EP0376893A3 (en) | 1988-12-30 | 1989-12-27 | Liquid laundry detergent compositions containing optical brighteners |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0376893A3 (en) |
JP (1) | JPH02227497A (en) |
DE (1) | DE3844341A1 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5873913A (en) * | 1994-06-23 | 1999-02-23 | Clariant Finance (Bvi) Limited | Optical brightening agents |
EP1752453A1 (en) | 2005-08-04 | 2007-02-14 | Clariant International Ltd. | Storage stable solutions of optical brighteners |
CN113574160A (en) * | 2019-03-19 | 2021-10-29 | 宝洁公司 | Method for washing fabrics |
US11878077B2 (en) | 2019-03-19 | 2024-01-23 | The Procter & Gamble Company | Fibrous water-soluble unit dose articles comprising water-soluble fibrous structures |
US12031254B2 (en) | 2019-03-19 | 2024-07-09 | The Procter & Gamble Company | Process of reducing malodors on fabrics |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS483889U (en) * | 1971-05-26 | 1973-01-17 | ||
JPS515412B1 (en) * | 1970-09-28 | 1976-02-19 | ||
FR2378119A1 (en) * | 1977-01-22 | 1978-08-18 | Hoechst Ag | Optical brightener compsns. for treating synthetic textiles - also contain oxyalkylated prim. aliphatic amine, opt. nonionic dispersant and water or poly:alkylene glycol! diluent |
US4233167A (en) * | 1979-06-14 | 1980-11-11 | S. C. Johnson & Son, Inc. | Liquid detergent softening and brightening composition |
SU804678A1 (en) * | 1978-06-19 | 1981-02-15 | Предприятие П/Я М-5400 | Liquid preparate for optical bleaching |
DD230531A3 (en) * | 1983-07-21 | 1985-12-04 | Bitterfeld Chemie | METHOD FOR PRODUCING AN OPTICAL LIGHTING AGENT OF THE BISTRIAZINYLAMINOSTILS SERIES |
EP0275694A1 (en) * | 1986-12-24 | 1988-07-27 | Unilever Plc | Concentrated liquid fabric softener with whitener |
GB2204609A (en) * | 1987-05-11 | 1988-11-16 | Sandoz Ltd | Liquid detergent/softener compositions |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1234486A (en) * | 1968-07-20 | 1971-06-03 | ||
GB1281189A (en) * | 1969-12-20 | 1972-07-12 | Ciab Geigy U K Ltd | Method of whitening triazine-type optical bleaching agents |
JPS591598A (en) * | 1982-06-25 | 1984-01-06 | 花王株式会社 | Detergent composition |
-
1988
- 1988-12-30 DE DE19883844341 patent/DE3844341A1/en not_active Withdrawn
-
1989
- 1989-12-27 EP EP19890810985 patent/EP0376893A3/en not_active Withdrawn
- 1989-12-27 JP JP33681589A patent/JPH02227497A/en active Pending
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS515412B1 (en) * | 1970-09-28 | 1976-02-19 | ||
JPS483889U (en) * | 1971-05-26 | 1973-01-17 | ||
FR2378119A1 (en) * | 1977-01-22 | 1978-08-18 | Hoechst Ag | Optical brightener compsns. for treating synthetic textiles - also contain oxyalkylated prim. aliphatic amine, opt. nonionic dispersant and water or poly:alkylene glycol! diluent |
SU804678A1 (en) * | 1978-06-19 | 1981-02-15 | Предприятие П/Я М-5400 | Liquid preparate for optical bleaching |
US4233167A (en) * | 1979-06-14 | 1980-11-11 | S. C. Johnson & Son, Inc. | Liquid detergent softening and brightening composition |
DD230531A3 (en) * | 1983-07-21 | 1985-12-04 | Bitterfeld Chemie | METHOD FOR PRODUCING AN OPTICAL LIGHTING AGENT OF THE BISTRIAZINYLAMINOSTILS SERIES |
EP0275694A1 (en) * | 1986-12-24 | 1988-07-27 | Unilever Plc | Concentrated liquid fabric softener with whitener |
GB2204609A (en) * | 1987-05-11 | 1988-11-16 | Sandoz Ltd | Liquid detergent/softener compositions |
Non-Patent Citations (5)
Title |
---|
CHEMICAL ABSTRACTS, vol. 110, no. 22, 29 May 1989 Columbus, Ohio, USA page 128; right-hand column; ref. no. 195198R * |
CHEMICAL ABSTRACTS, vol. 79, no. 22, 3 December 1973 Columbus, Ohio, USA page 59; left-hand column; ref. no. 127576D & JP-U-48 003 889 (SUMITOMO CHEMICAL CO., LTD.) * |
CHEMICAL ABSTRACTS, vol. 85, no. 12, 20 September 1976 Columbus, Ohio, USA page 129; right-hand column; ref. no. 80081 & JP-A-51 005 412 (SHINNICHI SOKAKO CO.,LTD.) * |
CHEMICAL ABSTRACTS, vol. 95, no. 6, 10 August 1981 Columbus, Ohio, USA page 72; right-hand column; ref. no. 44673N & SU-A-804678 (A.I. BUKHANKO ET AL.) * |
JOURNAL OF THE AMERICAN OIL CHEMISTS' SOCIETY. vol. 65, no. 4, April 1988, CHAMPAIGN US pages 679 - 683; W.R. FINDLEY: "FLUORESCENT WHITENING AGENTS FOR MODERN DETERGENTS" * |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5873913A (en) * | 1994-06-23 | 1999-02-23 | Clariant Finance (Bvi) Limited | Optical brightening agents |
EP1752453A1 (en) | 2005-08-04 | 2007-02-14 | Clariant International Ltd. | Storage stable solutions of optical brighteners |
US8221588B2 (en) | 2005-08-04 | 2012-07-17 | Clariant Finance (Bvi) Limited | Storage stable solutions of optical brighteners |
CN113574160A (en) * | 2019-03-19 | 2021-10-29 | 宝洁公司 | Method for washing fabrics |
US11878077B2 (en) | 2019-03-19 | 2024-01-23 | The Procter & Gamble Company | Fibrous water-soluble unit dose articles comprising water-soluble fibrous structures |
US12031254B2 (en) | 2019-03-19 | 2024-07-09 | The Procter & Gamble Company | Process of reducing malodors on fabrics |
Also Published As
Publication number | Publication date |
---|---|
JPH02227497A (en) | 1990-09-10 |
DE3844341A1 (en) | 1990-07-05 |
EP0376893A3 (en) | 1991-08-07 |
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