US3560389A - Liquid detergent bleach composition - Google Patents
Liquid detergent bleach composition Download PDFInfo
- Publication number
- US3560389A US3560389A US661761A US3560389DA US3560389A US 3560389 A US3560389 A US 3560389A US 661761 A US661761 A US 661761A US 3560389D A US3560389D A US 3560389DA US 3560389 A US3560389 A US 3560389A
- Authority
- US
- United States
- Prior art keywords
- sodium
- detergent
- detergents
- alcohol
- composition
- 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.)
- Expired - Lifetime
Links
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
- C11D3/16—Organic compounds
- C11D3/34—Organic compounds containing sulfur
- C11D3/3418—Toluene -, xylene -, cumene -, benzene - or naphthalene sulfonates or sulfates
-
- 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
- C11D3/395—Bleaching agents
- C11D3/3956—Liquid compositions
Definitions
- a liquid detergent bleach composition comprising an aqueous mixture of a detergent, a bleaching or oxidizing agent, and a hydrotrope in :which the components are present in such an amount so as to provide a clear liquid at room temperature is disclosed.
- This invention relates to a stable, liquid detergentbleach composition.
- sodium lauryl ether sulphate which is a commercially available water-soluble detergent, is incompatible with sodium hypochlorite in that when the two are mixed a heavy precipitate of insoluble matter is produced making the product unsuitable as a commercial proposition.
- hydrotropes such as for example, sodium xylene sulphonate, which are known clarifying agents, when added to such a preparation not only produce a liquid which is clear at room temperature and in some cases even down to C., but also that the mixture of the three components retains its detergent power, and retains its oxidising power over a length of time at least substantially equal to that which would be expected from sodium hypochlorite alone.
- the present invention provides a liquid detergent bleach composition, comprising an aqueous mixture of a detergent, a bleaching or oxidising agent, and a hydrotrope which is an alkali metal or alkaline earth metal salt of a monoor polyalkylated benzene or naphthalene sulphonate of which the alkyl groups contain from 1 to 4 carbon atoms, the three components being present in amounts such as to provide a clear liquid at room temperature.
- alkalinity of the composition Whilst such three component compositions are stable, we have also found that there is an optimum level for alkalinity of the composition due to the presence of hydroxyl ions and this alkalinity is preferably between 1 and 2% expressed in terms of free sodium hydroxide, although in fact the alkalinity may be due to other cations provided by compounds such as magnesium hydroxide, potassium hydroxide or lithium hydroxide.
- the optimum alkalinity depends upon the particular formulation and quality of the raw materials. Thus, for example, when the bleaching agent is sodium hypochlorite, it is preferred to use a quality of sodium hypochlorite with the lowest possible sodium chloride content, but a higher content of sodium chloride can be tolerated by appropriate adjustment of the alkalinity of the mixture.
- the detergent of the present composition may be any of those detergents commonly employed and may be used alone, or in admixture with other detergents.
- a first class of detergents which may be employed in the present compositions is the metal alcohol sulphates of which the alcohol contains from 6 to 22 carbon atoms.
- the alcohol may be a synthetic alcohol, a branched chain alcohol or a fatty alcohol.
- the alcohols may be pure or may be mixtures of alcohols, particularly such mixtures of fatty alcohols as are available commercially.
- suitable detergents in this class include sodium lauryl sulphate, sodium decyl sulphate, sodium myristyl sulphate, and the corresponding lithium salts.
- the metal component of the detergents of this class is preferably an alkali metal such as sodium or lithium, or an alkaline earth metal such as magnesium.
- the second class of detergents which may be employed in the present compositions is the metal alcohol ether sulphates, of which the alcohol is the same as that of the first class of detergents and of which the metal is preferably an alkali metal or an alkaline earth metal.
- the alcohol ethers from which the second class of detergents is derived are made by reacting the alcohol with an olefin oxide.
- the preferred alcohol ethers are made by reacting the alcohol with ethylene oxide to give an ethoxylated alcohol of which the average composition comprises from 1 to 4 mols of ethylene oxide per mol of alcohol.
- this class of detergent are sodium lauryl ether sulphate (including the commercially available material which also comprises sodium decyl ether sulphate and sodium myristyl ether sulphate) and lithium lauryl ether sulphate.
- a third class of detergent which may be employed in the present compositions is the alkali metal alkyl aryl sulphonates including for example sodium dodecyl benzene sulphonate and lithium dodecyl benzene sulphonate.
- a fourth class of detergents which may be employed in the present compositions is the oxidation products of fatty amines and derivatives thereof, which products are generally known in the detergent industry as amine oxides and which are employed as detergents in their own right or as builders.
- An example of a suitable detergent in this class is dimethyl cocoamine oxide.
- the detergents may be employed alone or in admixture with one another, including mixtures of detergents within the same class and mixtures of detergents in different classes. While all the above mentioned detergents are compatible with one another, detergents in other classes not specifically mentioned may not be entirely compatible with one another and mixtures of incompatible detergents should be avoided. In particular, it is preferred not to employ mixtures of cationic and anionic detergents.
- the hydrotropes employed in the present compositions are a well known family of clarifying agents comprising the alkali metal or alkaline earth metal salts of monoor polyalkylated benzene or naphthalene sulphonates of which the alkyl groups contain from 1 to 4 carbon atoms.
- the preferred hydrotrope is sodium xylene sulphonate which is commercially available as an unspecified mixture of the isomeric sulphonates, but other hydrotropes, such as the water-soluble alkali metal and alkaline earth metal salts, e.g., the sodium, patassium, lithium and magnesium salts of xylene or toluene sulphonic acid may be used.
- the range of proportions of the three components of the mixture may be varied within wide limits but will generally be interrelated in the sense that the amount of hydrotrope required will depend upon the amount of detergent present and the nature of the detergent and the amount of detergent which may be added to the composition will depend upon the amount of hydrotrope present.
- the ratio by weight of hydrotrope to detergent Will be from 2:1 to 1:2, with a preferred ratio of 1:1 for most general commercial purposes.
- the ratio may depend upon the particular detergent may be increased to 5:1 or more for detergents which are not readily water-soluble, such as sodium lauryl sulphate.
- the amount of bleaching or oxidising agent may be varied widely and the compositions of the present invention include not only compositions which are primarily regarded as bleaching or oxidising compositions and which contain a large amount of bleaching or oxidis ing agent and a small amount of detergent for wetting purposes, such as may be used for sterilizing dairy equipment, but also compositions which are primarily regarded as detergent compositions and which contain a large amount of detergent and a small amount of bleaching or oxidising agent, such as may be used for washing diapers.
- the bleaching or oxidising agent is preferably sodium hypochlorite or lithium hypochlorite, but other agents may be. employed.
- composition may, of course, contain conventional additives such as odorifiers, builders, brightening agents and solubilisers, provided that they are compatible with the bleaching or oxidising agent.
- the amount of detergent, sodium lauryl ethersulphate, determined at the end of the test period was substantially the same as at the beginning,
- compositions which have a clarity at ambient temperature, and 0 C., and stability, comparable to the composition of Example 15.
- a liquid detergent bleach composition consisting essentially of (a) water; (b) a detergent selected from the group consisting of alkali metal and alkaline earth metal alcohol sulphates of which the alcohol contains from 6 to 22 carbon atoms, alkali metal and alkaline earth metal alcohol ether sulphates of which the alcohol contains from 6 to 22 carbon atoms and an average of 1 to 4 moles of ethylene oxide per mole of alcohol, alkali metal alkyl benzene sulphonates and fatty amine oxides; (c) an alkali metal hypochlorite bleaching agent; and (d) a hydrotrope selected from the group consisting of alkali metal and alkaline earth metal salts of monoand polyalkylated benzene and naphthalene sulphonates of which the alkyl groups contain from 1 to 4 carbon atoms; the proportions of the components (a), (b), (c) and (d) being interrelated such as to provide a clear liquid at room temperature.
- composition as claimed in claim 1 wherein the alkalinity of said composition due to the presence of hydroxyl ions and expressed in terms of free sodium hydroxide, is between 1 and 2%.
- composition as claimed in claim 1 wherein the ratio by weight of hydrotrope to detergent in the composition is from 2:1 to 1:2.
- composition as claimed in claim 1, wherein said bleaching agent is selected from the group consisting of sodium hypochlorite and lithium hypochlorite.
- composition as claimed in claim 1, wherein said detergent is sodium lauryl ether sulphate.
- composition as claimed in claim 1, wherein said detergent is sodium or lithium lauryl sulphate.
Landscapes
- 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)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB36041/66A GB1128411A (en) | 1966-08-11 | 1966-08-11 | Detergent-bleach compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
US3560389A true US3560389A (en) | 1971-02-02 |
Family
ID=10384291
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US661761A Expired - Lifetime US3560389A (en) | 1966-08-11 | 1967-08-08 | Liquid detergent bleach composition |
Country Status (5)
Country | Link |
---|---|
US (1) | US3560389A (no) |
AT (1) | AT294750B (no) |
DE (1) | DE1617067A1 (no) |
GB (1) | GB1128411A (no) |
ZA (1) | ZA674667B (no) |
Cited By (38)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3876551A (en) * | 1972-02-14 | 1975-04-08 | Int Flavors & Fragrances Inc | Perfumed aqueous hypochlorite composition and method for preparation of same |
US3962112A (en) * | 1974-08-26 | 1976-06-08 | Charles William Shaheen | Composition and process for removing sulfur dioxide from combustion gases |
US4051056A (en) * | 1974-09-09 | 1977-09-27 | The Procter & Gamble Company | Abrasive scouring compositions |
US4071463A (en) * | 1975-09-11 | 1978-01-31 | The Dow Chemical Company | Stable cleaning agents of hypochlorite bleach and detergent |
DE2855776A1 (de) * | 1977-12-22 | 1979-06-28 | Unilever Nv | Fluessiges reinigungsmittel |
US4235732A (en) * | 1978-02-08 | 1980-11-25 | The Procter & Gamble Company | Liquid bleaching compositions |
US4240919A (en) * | 1978-11-29 | 1980-12-23 | S. C. Johnson & Son, Inc. | Thixotropic abrasive liquid scouring composition |
US4282109A (en) * | 1979-05-30 | 1981-08-04 | Reckitt & Colman Products Limited | Aqueous hypochlorite solutions |
US4289640A (en) * | 1974-01-21 | 1981-09-15 | Colgate-Palmolive Company | Cleaning compositions |
US4377489A (en) * | 1981-03-16 | 1983-03-22 | Ceil Clean Corporation, Inc. | Inorganic persulfate cleaning solution for acoustic materials |
US4388204A (en) * | 1982-03-23 | 1983-06-14 | The Drackett Company | Thickened alkali metal hypochlorite compositions |
US4390448A (en) * | 1981-10-22 | 1983-06-28 | International Flavors & Fragrances Inc. | Perfumed stable aqueous hypochlorite bleach compositions containing 2-methyl-2-octanol and thickened variation thereof |
US4599186A (en) * | 1984-04-20 | 1986-07-08 | The Clorox Company | Thickened aqueous abrasive scouring cleanser |
US4657692A (en) * | 1984-04-20 | 1987-04-14 | The Clorox Company | Thickened aqueous abrasive scouring cleanser |
US4783283A (en) * | 1985-05-28 | 1988-11-08 | The Procter & Gamble Company | Cleaning compositions |
US4842771A (en) * | 1986-09-29 | 1989-06-27 | Akzo N.V. | Thickened aqueous cleaning compositions |
US4853146A (en) * | 1987-01-24 | 1989-08-01 | Akzo N.V. | Thickening compositions and thickened aqueous acid solutions |
US4863633A (en) * | 1987-08-07 | 1989-09-05 | The Clorox Company | Mitigation of stress-cracking in stacked loads of fragranced bleach-containing bottles |
US4946619A (en) * | 1988-07-19 | 1990-08-07 | The Clorox Company | Solubilization of brighter in liquid hypochlorite |
US5011538A (en) * | 1987-11-17 | 1991-04-30 | The Clorox Company | Viscoelastic cleaning compositions and methods of use therefor |
US5034150A (en) * | 1989-05-03 | 1991-07-23 | The Clorox Company | Thickened hypochlorite bleach solution and method of use |
US5055219A (en) * | 1987-11-17 | 1991-10-08 | The Clorox Company | Viscoelastic cleaning compositions and methods of use therefor |
US5080826A (en) * | 1987-08-07 | 1992-01-14 | The Clorox Company | Stable fragranced bleaching composition |
US5227366A (en) * | 1987-08-07 | 1993-07-13 | The Clorox Company | Mitigation of stress-cracking in fragranced bleach-containing bottles |
US5279758A (en) * | 1991-10-22 | 1994-01-18 | The Clorox Company | Thickened aqueous cleaning compositions |
EP0594314A1 (en) * | 1992-10-19 | 1994-04-27 | The Clorox Company | Composition and method for developing extensional viscosity in cleaning compositions |
US5389157A (en) * | 1988-05-20 | 1995-02-14 | The Clorox Company | Viscoelastic cleaning compositions with long relaxation times |
US5549842A (en) * | 1993-12-29 | 1996-08-27 | Reckitt & Colman Inc. | Thickened alkali metal hypochlorite composition |
US5705467A (en) * | 1991-10-22 | 1998-01-06 | Choy; Clement K. | Thickened aqueous cleaning compositions and methods of use |
US5804545A (en) * | 1993-11-24 | 1998-09-08 | West Argo, Inc. | Stable alkaline chlorine compositions |
US5833764A (en) * | 1987-11-17 | 1998-11-10 | Rader; James E. | Method for opening drains using phase stable viscoelastic cleaning compositions |
EP0984059A1 (en) * | 1998-09-01 | 2000-03-08 | The Procter & Gamble Company | Bleaching compositions |
EP0990696A1 (en) * | 1998-10-01 | 2000-04-05 | The Procter & Gamble Company | Stable bleaching compositions |
EP0992576A1 (en) * | 1998-10-01 | 2000-04-12 | The Procter & Gamble Company | Stable bleaching compositions |
US6413925B2 (en) | 1998-08-26 | 2002-07-02 | The Clorox Company | Method for increasing brightness retention of laundered fabrics |
US6506718B1 (en) | 1998-09-01 | 2003-01-14 | The Procter & Gamble Company | Bleaching compositions |
US9637708B2 (en) | 2014-02-14 | 2017-05-02 | Ecolab Usa Inc. | Reduced misting and clinging chlorine-based hard surface cleaner |
EP3068759A4 (en) * | 2013-11-13 | 2017-06-28 | The Clorox Company | Mesitylene sulfonate compositions and methods thereof |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL134221C (no) * | 1969-08-29 | Unilever Nv | ||
FR2570713B1 (fr) * | 1984-09-21 | 1987-08-21 | Lesieur Cotelle | Compositions de nettoyage aqueuses epaissies |
FR2572419B1 (fr) * | 1984-10-31 | 1988-01-08 | Diversey France | Composition detergente et desinfectante, son utilisation notamment dans le domaine agricole et alimentaire, en particulier dans celui du nettoyage des machines a vendanger |
NZ218730A (en) * | 1986-01-03 | 1990-04-26 | Bristol Myers Co | Bleaching composition including thickening agent |
EP0265979B2 (en) * | 1986-09-29 | 1998-06-03 | Akzo Nobel N.V. | Thickened aqueous cleaning compositions |
ES2007221A6 (es) * | 1988-05-05 | 1989-06-01 | Henkel Iberica | Composicion blanqueante a base de hipocloritos alcalinos y procedimiento para su obtencion. |
US4917814A (en) * | 1988-08-11 | 1990-04-17 | The Drackett Company | Pigmented hypochlorite compositions |
DE102005062012A1 (de) * | 2005-12-22 | 2007-06-28 | Henkel Kgaa | Handgeschirrspülmittel |
-
0
- ZA ZA674667D patent/ZA674667B/xx unknown
-
1966
- 1966-08-11 GB GB36041/66A patent/GB1128411A/en not_active Expired
-
1967
- 1967-08-08 US US661761A patent/US3560389A/en not_active Expired - Lifetime
- 1967-08-09 AT AT737767A patent/AT294750B/de not_active IP Right Cessation
- 1967-08-10 DE DE19671617067 patent/DE1617067A1/de active Pending
Cited By (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3876551A (en) * | 1972-02-14 | 1975-04-08 | Int Flavors & Fragrances Inc | Perfumed aqueous hypochlorite composition and method for preparation of same |
US4289640A (en) * | 1974-01-21 | 1981-09-15 | Colgate-Palmolive Company | Cleaning compositions |
US3962112A (en) * | 1974-08-26 | 1976-06-08 | Charles William Shaheen | Composition and process for removing sulfur dioxide from combustion gases |
US4051056A (en) * | 1974-09-09 | 1977-09-27 | The Procter & Gamble Company | Abrasive scouring compositions |
US4071463A (en) * | 1975-09-11 | 1978-01-31 | The Dow Chemical Company | Stable cleaning agents of hypochlorite bleach and detergent |
DE2855776A1 (de) * | 1977-12-22 | 1979-06-28 | Unilever Nv | Fluessiges reinigungsmittel |
US4235732A (en) * | 1978-02-08 | 1980-11-25 | The Procter & Gamble Company | Liquid bleaching compositions |
US4240919A (en) * | 1978-11-29 | 1980-12-23 | S. C. Johnson & Son, Inc. | Thixotropic abrasive liquid scouring composition |
US4282109A (en) * | 1979-05-30 | 1981-08-04 | Reckitt & Colman Products Limited | Aqueous hypochlorite solutions |
US4377489A (en) * | 1981-03-16 | 1983-03-22 | Ceil Clean Corporation, Inc. | Inorganic persulfate cleaning solution for acoustic materials |
US4485028A (en) * | 1981-03-16 | 1984-11-27 | Ceil Clean Corporation, Inc. | Inorganic persulfate cleaning solution for acoustic materials |
US4390448A (en) * | 1981-10-22 | 1983-06-28 | International Flavors & Fragrances Inc. | Perfumed stable aqueous hypochlorite bleach compositions containing 2-methyl-2-octanol and thickened variation thereof |
US4388204A (en) * | 1982-03-23 | 1983-06-14 | The Drackett Company | Thickened alkali metal hypochlorite compositions |
US4599186A (en) * | 1984-04-20 | 1986-07-08 | The Clorox Company | Thickened aqueous abrasive scouring cleanser |
US4657692A (en) * | 1984-04-20 | 1987-04-14 | The Clorox Company | Thickened aqueous abrasive scouring cleanser |
US4783283A (en) * | 1985-05-28 | 1988-11-08 | The Procter & Gamble Company | Cleaning compositions |
US4842771A (en) * | 1986-09-29 | 1989-06-27 | Akzo N.V. | Thickened aqueous cleaning compositions |
US4853146A (en) * | 1987-01-24 | 1989-08-01 | Akzo N.V. | Thickening compositions and thickened aqueous acid solutions |
EP0518451A1 (en) * | 1987-08-07 | 1992-12-16 | The Clorox Company | Homogeneous fragrance preblend |
US5080826A (en) * | 1987-08-07 | 1992-01-14 | The Clorox Company | Stable fragranced bleaching composition |
US5227366A (en) * | 1987-08-07 | 1993-07-13 | The Clorox Company | Mitigation of stress-cracking in fragranced bleach-containing bottles |
US4863633A (en) * | 1987-08-07 | 1989-09-05 | The Clorox Company | Mitigation of stress-cracking in stacked loads of fragranced bleach-containing bottles |
US5055219A (en) * | 1987-11-17 | 1991-10-08 | The Clorox Company | Viscoelastic cleaning compositions and methods of use therefor |
US5833764A (en) * | 1987-11-17 | 1998-11-10 | Rader; James E. | Method for opening drains using phase stable viscoelastic cleaning compositions |
US5011538A (en) * | 1987-11-17 | 1991-04-30 | The Clorox Company | Viscoelastic cleaning compositions and methods of use therefor |
US5389157A (en) * | 1988-05-20 | 1995-02-14 | The Clorox Company | Viscoelastic cleaning compositions with long relaxation times |
US4946619A (en) * | 1988-07-19 | 1990-08-07 | The Clorox Company | Solubilization of brighter in liquid hypochlorite |
US5034150A (en) * | 1989-05-03 | 1991-07-23 | The Clorox Company | Thickened hypochlorite bleach solution and method of use |
US5279758A (en) * | 1991-10-22 | 1994-01-18 | The Clorox Company | Thickened aqueous cleaning compositions |
US5705467A (en) * | 1991-10-22 | 1998-01-06 | Choy; Clement K. | Thickened aqueous cleaning compositions and methods of use |
EP0594314A1 (en) * | 1992-10-19 | 1994-04-27 | The Clorox Company | Composition and method for developing extensional viscosity in cleaning compositions |
US5462689A (en) * | 1992-10-19 | 1995-10-31 | The Clorox Company | Composition and method for developing extensional viscosity in cleaning compositions |
US5916859A (en) * | 1992-10-19 | 1999-06-29 | The Clorox Company | Hexadecyl amine oxide/counterion composition and method for developing extensional viscosity in cleaning compositions |
TR28567A (tr) * | 1992-10-19 | 1996-10-18 | Clorox Co | Temizleyici bilesimlerde genlesme viskozitesi gelistirmeye mahsus yöntem ve bilesim |
US5804545A (en) * | 1993-11-24 | 1998-09-08 | West Argo, Inc. | Stable alkaline chlorine compositions |
US5549842A (en) * | 1993-12-29 | 1996-08-27 | Reckitt & Colman Inc. | Thickened alkali metal hypochlorite composition |
US6413925B2 (en) | 1998-08-26 | 2002-07-02 | The Clorox Company | Method for increasing brightness retention of laundered fabrics |
EP0984059A1 (en) * | 1998-09-01 | 2000-03-08 | The Procter & Gamble Company | Bleaching compositions |
WO2000012668A1 (en) * | 1998-09-01 | 2000-03-09 | The Procter & Gamble Company | Bleaching compositions |
US6649583B2 (en) | 1998-09-01 | 2003-11-18 | Procter & Gamble Company | Bleaching compositions |
US6506718B1 (en) | 1998-09-01 | 2003-01-14 | The Procter & Gamble Company | Bleaching compositions |
EP0990696A1 (en) * | 1998-10-01 | 2000-04-05 | The Procter & Gamble Company | Stable bleaching compositions |
EP0992576A1 (en) * | 1998-10-01 | 2000-04-12 | The Procter & Gamble Company | Stable bleaching compositions |
WO2000018866A1 (en) * | 1998-10-01 | 2000-04-06 | The Procter & Gamble Company | Stable bleaching compositions |
EP3068759A4 (en) * | 2013-11-13 | 2017-06-28 | The Clorox Company | Mesitylene sulfonate compositions and methods thereof |
US9637708B2 (en) | 2014-02-14 | 2017-05-02 | Ecolab Usa Inc. | Reduced misting and clinging chlorine-based hard surface cleaner |
US10220421B2 (en) | 2014-02-14 | 2019-03-05 | Ecolab Usa Inc. | Reduced misting and clinging chlorine-based hard surface cleaner |
US10821484B2 (en) | 2014-02-14 | 2020-11-03 | Ecolab Usa Inc. | Reduced misting and clinging chlorine-based hard surface cleaner |
US11331696B2 (en) | 2014-02-14 | 2022-05-17 | Ecolab Usa Inc. | Reduced misting and clinging chlorine based hard surface cleaner |
Also Published As
Publication number | Publication date |
---|---|
DE1617067A1 (de) | 1971-02-11 |
GB1128411A (en) | 1968-09-25 |
AT294750B (de) | 1971-12-10 |
ZA674667B (no) |
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