EP0199404B1 - Flüssige Reinigungsmittel mit einer anionischen oberflächenaktiven Verbindung, einem Verstärker und einem proteolytischen Enzym - Google Patents

Flüssige Reinigungsmittel mit einer anionischen oberflächenaktiven Verbindung, einem Verstärker und einem proteolytischen Enzym Download PDF

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EP0199404B1
EP0199404B1 EP86200585A EP86200585A EP0199404B1 EP 0199404 B1 EP0199404 B1 EP 0199404B1 EP 86200585 A EP86200585 A EP 86200585A EP 86200585 A EP86200585 A EP 86200585A EP 0199404 B1 EP0199404 B1 EP 0199404B1
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replaced
acid
composition according
water
composition
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EP0199404A3 (en
EP0199404A2 (de
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Manuel Garcia Venegas
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Procter and Gamble Co
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Procter and Gamble Co
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    • 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
    • C11D3/38—Products with no well-defined composition, e.g. natural products
    • C11D3/386—Preparations containing enzymes, e.g. protease or amylase
    • C11D3/38663—Stabilised liquid enzyme compositions

Definitions

  • the present invention relates to heavy-duty liquid laundry detergent compositions containing anionic synthetic surfactant, detergency builder, specific proteolytic enzyme and calcium ion.
  • the compositions provide improved cleaning performance, particularly through-the-wash, of enzyme-sensitive stains such as grass, blood, gravy and chocolate pudding.
  • Laundry detergents containing high levels of anionic surfactant and builder, and capable of providing superior cleaning performance are currently available. Some of these compositions also contain enzymes to enhance removal of enzyme-sensitive stains. However, it is believed that such compositions are enzyme-limited in that they can denature and expose stains to enzymatic action faster than currently available enzymes can cleave and break up the stains.
  • Enzyme performance can also be limited by a lack of adequate stability in liquid detergents.
  • the stabilization of enzymes is particularly difficult in built, heavy-duty liquid detergents containing high levels of anionic surfactant and water.
  • Anionic surfactants, especially alkyl sulfates, tend to denature enzymes and render them inactive.
  • Detergent builders can sequester the calcium ion needed for enzyme activity and/or stability.
  • the compositions can contain 10-60% surfactant, including anionics, and up to 40% builder.
  • U.S. Patent 4,404,115, Tai, issued September 13, 1983 discloses liquid cleaning compositions, preferably built liquid detergents, containing enzyme, 1-15% alkali metal pentaborate, 0-15% alkali metal sulfite, and 0-15% of a polyol having 2-6 hydroxy groups.
  • the compositions can contain 1-60% surfactant, preferably a mixture of anionic and nonionic in a weight ratio of 6:1 to 1:1, with or without soap.
  • the compositions also preferably contain 5-50% builder.
  • the compositions preferably contain from about 20% to 50% surfactant, which can be anionic. In a preferred embodiment, the compositions contain about 3% to 15% of a saturated fatty acid. They are othervise substantially free of builders, but can contain minor amounts of sequestrants.
  • the enzymes are said to be useful in laundry detergents, both liquid and granular. They can be combined with surfactants (including anionics), builders, bleach and/or fluorescent whitening agents, but there is no disclosure of specific detergent compositions.
  • Copending European Patent application EP-A-199 405 discloses liquid detergent compositions comprising the proteolytic enzymes herein and boric acid.
  • This invention relates to heavy-duty liquid laundry detergent compositions comprising, by weight:
  • the liquid detergents of the present invention contain, as essential components, anionic synthetic surfactant, detergency builder, specific proteolytic enzyme, calcium ion, and water.
  • the compositions herein provide improved cleaning performance, particularly through-the-wash, on enzyme-sensitive stains such as grass, blood, gravy and chocolate pudding.
  • anionic surfactant and builder in the present compositions provides an effective matrix for denaturing stains and exposing sites to enzymatic action.
  • the anionic surfactant is believed to be the primary denaturing agent, whereas the builder controls water hardness that would otherwise complex the anionic surfactant and interfere with its denaturing action.
  • the surfactant and builder matrix herein can denature and expose more sites on stains than currently available enzymes can cleave during the washing process. This is particularly true at low washing temperatures (e.g., in the range of 15°C to 35°C) where enzymes are catalytically slow.
  • the present proteolytic enzymes appear to be superior to other proteases in catalytic efficiency. They thus can take advantage of the stain denaturing power of the compositions herein and provide significant stain removal benefits. In contrast, they provide little or no benefits in detergent compositions containing less anionic surfactant and builder.
  • compositions of the present invention contain from 7% to 50%, preferably from about 10% to about 40%, and most preferably from about 15% to about 30%, by weight of an anionic synthetic surfactant.
  • anionic synthetic surfactants are disclosed in U.S. Patent 4,285,841, Barrat et al, issued August 25, 1981, and in U.S. Patent 3,929,678, Laughlin et al, issued December 30, 1975.
  • Useful anionic surfactants include the water-soluble salts, particularly the alkali metal, ammonium and alkylolammonium (e.g., monoethanolammonium or triethanolammonium) salts, of organic sulfuric reaction products having in their molecular structure an alkyl group containing from about 10 to about 20 carbon atoms and a sulfonic acid or sulfuric acid ester group.
  • water-soluble salts particularly the alkali metal, ammonium and alkylolammonium (e.g., monoethanolammonium or triethanolammonium) salts, of organic sulfuric reaction products having in their molecular structure an alkyl group containing from about 10 to about 20 carbon atoms and a sulfonic acid or sulfuric acid ester group.
  • alkyl is the alkyl portion of aryl groups.
  • alkyl sulfates especially those obtained by sulfating the higher alcohols (C8-C18 carbon atoms) such as those produced by reducing the glycerides of tallow or coconut oil; and the alkylbenzene sulfonates in which the alkyl group contains from about 9 to about 15 carbon atoms, in straight chain or branched chain configuration, e.g., those of the type described in U. S. Patents 2,220,099 and 2,477,383.
  • Especially valuable are linear straight chain alkylbenzene sulfonates in which the average number of carbon atoms in the alkyl group is from about 11 to 14.
  • anionic surfactants herein are the watersoluble salts of: paraffin sulfonates containing from about 8 to about 24 (preferably about 12 to 18) carbon atoms; alkyl glyceryl ether sulfonates, especially those ethers of C 8-18 alcohols (e.g., those derived from tallow and coconut oil); alkyl phenol ethylene oxide ether sulfates containing from about 1 to 4 units of ethylene oxide per molecule and from about 8 to about 12 carbon atoms in the alkyl group; and alkyl ethylene oxide ether sulfates containing about 1 to about 4 units of ethylene oxide per molecule and from about 10 to about 20 carbon atoms in the alkyl group.
  • Other useful anionic surfactants include the watersoluble salts of esters of alpha-sulfonated fatty acids containing from about 6 to 20 carbon atoms in the fatty acid group and from about 1 to 10 carbon atoms in the ester group; water-soluble salts of 2-acyloxy- alkane-1-sulfonic acids containing from about 2 to 9 carbon atoms in the acyl group and from about 9 to about 23 carbon atoms in the alkane moiety; water-soluble salts of olefin sulfonates containing from about 12 to 24 carbon atoms; and beta-alkyloxy alkane sulfonates containing from about 1 to 3 carbon atoms in the alkyl group and from about 8 to 20 carbon atoms in the alkane moiety.
  • Preferred anionic surfactants are the C10-C18 alkyl sulfates and alkyl ethoxy sulfates containing an average of up to about 4 ethylene oxide units per mole of alkyl sulfate, C11-C13 linear alkylbenzene sulfonates, and mixtures thereof.
  • compositions preferably contain from about 1% to about 5%, more preferably from about 2% to about 4%, by weight of unethoxylated alkyl sulfate.
  • alkyl sulfates are desired for best detergency performance, in part because they are very denaturing to stains.
  • compositions herein can optionally contain other synthetic surfactants known in the art, such as the nonionic, cationic, zwitterionic, and ampholytic surfactants described in the above-cited Barrat et al and Laughlin et al patents.
  • a preferred cosurfactant used at a level of from about 1% to about 25%, preferably from about 3% to about 15%, by weight of the composition, is an ethoxylated nonionic surfactant of the formula R1(OC2H4) n OH, wherein R1 is a C10-C16 alkyl group or a C8-C12 alkyl phenyl group, n is from about 3 to about 9, and said nonionic surfactant has an HLB (hydrophile-lipophile balance) of from about 6 to about 14, preferably from about 10 to about 13.
  • R1 is a C10-C16 alkyl group or a C8-C12 alkyl phenyl group
  • n is from about 3 to about 9
  • said nonionic surfactant has an HLB (hydrophile-lipophile balance) of from about 6 to about 14, preferably from about 10 to about 13.
  • Particularly preferred are condensation products of C12-C15 alcohols with from about 3 to about 8 moles of ethylene oxide per mole of alcohol, e.g., C12-C13 alcohol condensed with about 6.5 moles of ethylene oxide per mole of alcohol.
  • Preferred cosurfactants for use with the above ethoxylated nonionic surfactants are amides of the formula wherein R1 is an alkyl, hydroxyalkyl or alkenyl radical containing from about 8 to about 20 carbon atoms, and R2 and R3 are selected from the group consisting of hydrogen, methyl, ethyl, propyl, isopropyl, 2-hydroxyethyl, 2-hydroxypropyl, 3-hydroxypropyl, and said radicals additionally containing up to about 5 ethylene oxide units, provided at least one of R2 and R3 contains a hydroxyl group.
  • Preferred amides are the C8-C20 fatty acid alkylol amides in which each alkylol group contains from 1 to 3 carbon atoms, and additionally can contain up to about 2 ethylene oxide units. Particularly preferred are the C12-C16 fatty acid monoethanol and diethanol amides.
  • compositions herein preferably contain from about 5% to about 20%, preferably from about 6% to about 15%, more preferably from about 7% to about 12%, by weight of a mixture of the above ethoxylated nonionic surfactant and amide surfactant in a weight ratio of from about 4:1 to 1:4, preferably from about 3:1 to about 1:3, more preferably from about 2:1 to about 1:2.
  • the weight ratio of anionic synthetic surfactant (on an acid basis) to the total nonionic surfactant (both the ethoxylated nonionic and the amide) should be from about 2:1 to about 4:1, preferably from about 2.5:1 to about 3.5:1, to ensure that formation and adsorption of sufficient hardness surfactants at the oil/water interface to provide good greasy/oily soil removal.
  • cosurfactants used at a level of from about 0.5% to about 3%, preferably from about 0.7% to about 2%, by weight are the quaternary ammonium, amine or amine oxide surfactants described in U.S. Patent 4,507,219, Hughes, issued March 26, 1985.
  • compositions herein can contain di-long chain quaternary ammonium cationic surfactants (e.g., those having 2 chains, each containing an average of from about 16 to about 22 carbon atoms), such as disclosed in British Patent 2,041,968, Murphy, published September 19, 1979, the compositions preferably contain less than about 2%, more preferably less than about 1%, by weight of such surfactants. Most preferably, the compositions are substantially free of such surfactants because they appear to be detrimental to the stability of the proteolytic enzymes herein.
  • di-long chain quaternary ammonium cationic surfactants e.g., those having 2 chains, each containing an average of from about 16 to about 22 carbon atoms
  • the compositions preferably contain less than about 2%, more preferably less than about 1%, by weight of such surfactants.
  • the compositions are substantially free of such surfactants because they appear to be detrimental to the stability of the proteolytic enzymes herein.
  • compositions herein contain from 5% to 40%, preferably from about 8% to about 30%, more preferably from about 10% to about 25%, by weight of a detergent builder material.
  • the composition should contain at least about 20%, preferably from about 25% to about 60%, more preferably from about 30% to about 50%, by weight of the anionic synthetic surfactant and builder. Since the proteolytic enzymes herein appear to provide optimum performance benefits versus other enzymes when the builder to water hardness ratio is close to one, the compositions preferably contain sufficient builder to sequester from about 34 to about 171 mg/l, preferably from about 51 to about 137 mg/l of hardness. (2 to about 10, preferably from about 3 to about 8, grains per gallon of hardness).
  • Useful builders are fatty acids containing from about 10 to about 22 carbon atoms. Preferred are saturated fatty acids containing from about 10 to about 18, preferably from about 10 to about 14, carbon atoms. When present, the fatty acid preferably represents about 5% to about 20%, more preferably from about 8% to about 16%, by weight of the composition.
  • Suitable saturated fatty acids can be obtained from natural sources such as plant or animal esters (e.g., palm kernel oil, palm oil and coconut oil) or synthetically prepared (e.g., via the oxidation of petroleum or by hydrogenation of carbon monoxide via the Fisher-Tropsch process).
  • suitable saturated fatty acids for use in the compositions of this invention include capric, lauric, myristic, cocnut and palm kernel fatty acid.
  • Preferred are saturated coconut fatty acids; from about 5:1 to 1:1 (preferably about 3:1) weight ratio mixtures of lauric and myristic acid; mixtures of the above with minor amounts (e.g., 1%-30% of total fatty acid) of oleic acid; and palm kernel fatty acid.
  • Detergent builders useful herein also include the polycarboxylate, polyphosphonate and polyphosphate builders described in U.S. Patent 4,284,532, Leikhim et al, issued August 18, 1981. Water-soluble polycarboxylate builders, particularly citrates, are preferred of this group. Polycarboxylate builders preferably represent from about 1% to about 20% by weight of the composition.
  • Suitable polycarboxylate builders include the various aminopolycarboxylates, cycloalkane polycarboxylates, ether polycarboxylates, alkyl polycarboxylates, epoxy polycarboxylates, tetrahydrofuran polycarboxylates, benzene polycarboxylates, and polyacetal polycarboxylates.
  • polycarboxylate builders are sodium and potassium ethylenediaminetetraacetate; sodium and potassium nitrilotriacetate; the water-soluble salts of phytic acid, e.g., sodium and potassium phytates, disclosed in U.S. Patent 1,739,942, Eckey, issued March 27, 1956; the polycarboxylate materials described in U.S. Patent 3,364,103; and the water-soluble salts of polycarboxylate polymers and copolymers described in U.S. Patent 3,308,067, Diehl, issued March 7, 1967.
  • Useful detergent builders also include the water-soluble salts of polymeric aliphatic polycarboxylic acids having the following structural and physical characteristics: (a) a minimum molecular weight of about 350 calculated as to the acid form; (b) an equivalent weight of about 50 to about 80 calculated as to acid form; (3) at least 45 mole percent of the monomeric species having at least two carboxyl radicals separated from each other by not more than two carbon atoms: (d) the site of attachment of the polymer chain of any carboxyl-containing radical being separated by not more than three carbon atoms along the polymer chain from the site of attachment of the next carboxyl-containing radical.
  • Specific examples of such builders are the polymers and copolymers of itaconic acid, aconitic acid, maleic acid, mesaconic acid, fumaric acid, methylene malonic acid, and citraconic acid.
  • Suitable polycarboxylate builders include the water-soluble salts, especially the sodium and potassium salts, of mellitic acid, citric acid, pyromellitic acid, benzene pentacarboxylic acid, oxydiacetic acid, carboxymethyloxysuccinic acid, carboxymethyloxymalonic acid, cis-cyclohexanehexacarboxylic acid, cis-cyclopentanetetracarboxylic acid and oxydisuccinic acid.
  • water-soluble salts especially the sodium and potassium salts, of mellitic acid, citric acid, pyromellitic acid, benzene pentacarboxylic acid, oxydiacetic acid, carboxymethyloxysuccinic acid, carboxymethyloxymalonic acid, cis-cyclohexanehexacarboxylic acid, cis-cyclopentanetetracarboxylic acid and oxydisuccinic acid.
  • polycarboxylates for use herein are the polyacetal carboxylates described in U.S. Patent 4,144,226, issued March 13, 1979 to Crutchfield et al, and U.S. Patent 4,146,495, issued March 27, 1979 to Crutchfield et al.
  • detergent builders useful herein include the aluminosilicate ion exchange material described in U.S. Patent 4,405,483, Kuzel et al, issued September 20, 1983.
  • the compositions herein preferably contain from about 0.1% to about 1%, more preferably from about 0.2% to about 0.6%, by weight of water-soluble salts of ethylenediamine tetramethylenephosphonic acid, diethylenetriamine pentamethylenephosphonic acid, ethylenediamine tetraacetic acid, or diethylenetriamine pentaacetic acid to enhance cleaning performance when pretreating fabrics.
  • compositions of the present invention contain from 0.01% to 5%, preferably from about 0.1% to about 2%, by weight of the composition of Protease A as previously defined, or variants thereof in which the Gly at position 166 is replaced with Asn, Ser, Lys, Arg, His, Gln, Ala or Glu; the Gly at position 169 is replaced with Ser; the Met at position 222 is replaced with Gln, Phe, Cys, His, Asn, Glu, Ala or Thr; the Gly at position 166 is replaced with Lys and the Met at position 222 is replaced with Cys; or the Gly at position 169 is replaced with Ala and the Met at position 222 is replaced with Ala.
  • the above enzyme is preferably included in an amount sufficient to provide an activity of from about 0.001 to about 0.1, more preferably from about 0.005 to about 0.07, most preferably from about 0.01 to about 0.04, Anson units per gram of composition.
  • proteases herein are preferably purified, prior to incorporation in the finished composition, so that they have no detectable odor at a concentration of less than about 0.002 Anson units per gram in distilled water. They preferably have no detectable odor at a concentration of less than about 0.0025, more preferably less than about 0.003, Anson units per gram of distilled water.
  • Proteases herein can be odor purified by any method known in the art. Examples include the solvent precipitation methods described in Precipitation of the Enzymes and Their Stability in High Alcohol Concentrations by Bauer et al in the Israel J. Chem. 5(3), pages 117-20 (1967) and Enzyme Preparations by Sugiura et al and Yakusaigaku 1967, Volume 27(2), pages 135-9.
  • Solvent initiated precipitation of a crude commercial enzyme solution results in most of the enzymatic activity being precipitated from solution and most of the odor and color impurities remaining in the supernatant liquid. Decantation or centrifugation of the supernatant liquid from the precipitated enzyme results in an enzyme fraction with enriched enzymatic activity/gram and improved odor and color.
  • solvents or solvent pair combinations can be used to effect the desired precipitation.
  • methanol, ethanol, acetone, other organic solvents, and combinations of organic solvents with and without water can be used.
  • a highly preferred solvent is a combination of water and 30-70% by weight ethanol. This appears to be optimal to prevent enzyme deactivation and maximum recovery of activity.
  • Purfication of protease enzymes also provide benefits in the area of product color stability.
  • the composition also contains from 0.01 to 50, preferably from about 0.1 to about 30, more preferably from about 1 to about 20, millimoles of calcium ion per liter.
  • the level of calcium ion should be selected so that there is always some minimum level available for the enzyme, after allowing for complexation with builders, etc., in the composition.
  • Any water-soluble calcium salt can be used as the source of calcium ion, including calcium chloride, calcium formate, and calcium acetate.
  • a small amount of calcium ion generally from about 0.05 to about 0.4 millimoles per liter, is often also present in the composition due to calcium in the enzyme slurry and formula water.
  • compositions herein contain from 10% to 80%, preferably from about 20% to about 60%, more preferably from about 30% to about 50%, by weight of water.
  • compositions of the present invention can also contain other materials known in the art to enhance enzyme stability.
  • the compositions herein contain from about 0.1% to about 10%, more preferably from about 0.25% to about 5%, most preferably from about 0.5% to about 3%, by weight of boric acid or a compound capable of forming boric acid in the composition (calculated on the basis of the boric acid).
  • Boric acid is preferred, although other compounds such as boric oxide, borax and other alkali metal borates (e.g., sodium ortho-, meta- and pyroborate, and sodium pentaborate) are suitable.
  • Substituted boric acids e.g., phenylboronic acid, butane boronic acid, and p-bromo phenylboronic acid
  • polyols containing only carbon, hydrogen and oxygen atoms are polyols containing only carbon, hydrogen and oxygen atoms. They preferably contain from 2 to 6 carbon atoms and from 2 to 6 hydroxy groups. Examples include propylene glycol (especially 1,2 propane diol, which is preferred), ethylene, glycol, glycerol, sorbitol, mannitol, and glucose.
  • the polyol generally represents from about 1% to about 15%, preferably from about 1.5% to about 10%, by weight of the composition.
  • the weight ratio of polyol to boric acid is at least 1, more preferably at least about 1.3.
  • compositions can also contain the water-soluble, short chain carboxylates described in U.S. Patent 4,318,818, Letton et al, issued March 9, 1982.
  • the formates are preferred and can be used at levels of from about 0.05% to about 5%, preferably from about 0.2% to about 2%, most preferably from about 0.4% to about 1.5%, by weight of the composition.
  • compositions herein have an initial pH of from 6.5 to 9.5, preferably from about 7 to about 8.5, most preferably from about 7.2 to about 8.0, at a concentration of 0.2% by weight in distilled water at 20°C.
  • Preferred pH buffers include monoethanolamine and triethanolamine.
  • Monoethanolamine and triethanolamine also further enhance enzyme stability, and preferably are included at levels of from about 0.5% to about 10%, preferably from about 1% to about 4%, by weight of the composition.
  • optional components for use in the liquid detergents herein include soil removal agents, antiredeposition agents, suds regulants, hydrotropes, opacifiers, antioxidants, bactericides, dyes, perfumes, and brighteners known in the art.
  • Such optional components generally represent less than about 15%, preferably from about 1% to about 10%, by weight of the composition.
  • the following detergent compositions were prepared. in which about 20% by weight of the material has a value of u higher than 5 is dissolved at about 15% level in anhydrous ethanol; cooled to about 10°C; the insoluble portion ( ⁇ 20%) is filtered; and enough ethanol is distilled to reduce the ethanol level to within the level in the formula
  • Protease A of the present invention provided significantly better through-the-wash cleaning of enzyme-sensitive stains such as grass, blood, gravy, and/or chocolate pudding than did equivalent amounts (providing either 0.0012, 0.015 or 0.03 Anson units of activity per gram of composition) of the commercially available proteolytic enzymes Alcalase® (Novo Industries A.S.), Maxtase® (Gist-Brocades N.V.) and Maxacal® (Gist-Brocades N.V.). With pretreatment, Protease A provided smaller, generally directional benefits, but with some losses, versus Alcalase on enzyme-sensitive stains.
  • Protease A also provided similar benefits relative to Alcalase when the pH of Composition A in the wash solution was adjusted from 7.5 to 7.1, 7.3, 8.0 and 8.5.
  • Protease A provided similar benefits relative to Maxatase when the pH of Composition B in the wash solution was adjusted to 8.0 and 8.5.
  • Significant advantages on grass and chocolate pudding for Protease A were also obtained when the solution pH of Composition B was adjusted to 9.0 to 9.5, although the magnitude of the benefit was reduced at these higher pH's.
  • compositions C which was tested at a concentration of 900 ppm in water
  • D tested at a concentration of 2000 ppm in water
  • Protease A exhibited little or no benefit overall, and some negatives, on enzyme-sensitive stains, both through-the-wash and with pre-treatment, when compared with Alcalase.
  • Protease A was also significantly less effective than Maxacal on certain grass, blood, gravy and chocolate pudding stains when used in a granular detergent (which is not within the scope of the invention) containing 14.5% anionic surfactant, 33.7% sodium tripolyphosphate and 10.5% sodium carbonate builder, and which provided a pH of 10.0 at its usage concentration of 1500 ppm by weight in water at 20°C.
  • Protease A was generally equivalent to Alcalase in the same test, except for significant advantages on some blood stains. When the solution pH of the granular detergent was reduced to 8.0 and 8.5, Protease A was significantly less effective than Maxatase on grass, blood, gravy and chocolate pudding stains.
  • Protease A provided better overall cleaning and significant advantages on some stains when compared with Alcalase. Similar results were obtained when 260 ppm of the fatty acid and 60 ppm of citric acid were added to a wash solution containing 1800 ppm of Composition C (also thereby providing a composition which would have been within the scope of the invention if the acids were added directly to Composition C).
  • Preferred Composition E of the present invention contains 0.75% of a slurry of Protease A, providing an activity of 0.015 Anson units per gram of composition.

Claims (10)

  1. Flüssige Hochleistungswäschewaschdetergenszusammensetzung, umfassend, bezogen auf das Gewicht:
    (a) von 7 % bis 50 % eines anionischen synthetischen grenzflächenaktiven Mittels;
    (b) von 5 % bis 40 % eines Detergensgerüststoffes;
    (c) von 0,01 % bis 5 % des proteolytischen Enzyms, welches durch die folgende Aminosäuresequenz gekennzeichnet ist:
    Figure imgb0010
    Figure imgb0011
    oder worin Gly an der Position 166 durch Asn, Ser, Lys, Arg, His, Gln, Ala oder Glu ersetzt ist; Gly an der Position 169 durch Ser ersetzt ist; Met an der Position 222 durch Gln, Phe, Cys, His, Asn, Glu, Ala oder Thr ersetzt ist; Gly an der Position 166 durch Lys ersetzt ist und Met an der Position 222 durch Cys ersetzt ist; oder Gly an der Position 169 durch Ala ersetzt ist und Met an der Position 222 durch Ala ersetzt ist;
    (d) von 0,01 bis 50 Millimol Calciumionen je Liter an Zusammensetzung; und
    (e) von 10 % bis 80 % Wasser;
    welche Zusammensetzung mindestens 20 % von (a) + (b) enthält, und einen Anfangs-pH-Wert von 6,5 bis 9,5 bei einer Konzentration von 0,2 % in Wassser bei 20°C aufweist.
  2. Zusammensetzung nach Anspruch 1, welche etwa 15 % bis etwa 30% des anionischen synthetischen grenzflächnaktiven Mittels umfaßt.
  3. Zusammensetzung nach Anspruch 2, welche etwa 1 % bis etwa 5 % eines nicht-ethoxylierten C₁₀-C₁₈-Alkylsulfat-grenzflächenaktiven Mittels enthält.
  4. Zusammensetzung nach Anspruch 2, welche etwa 5 % bis etwa 20% einer gesättigten Fettsäure mit etwa 10 bis etwa 14 Kohlenstoffatomen enthält.
  5. Zusammensetzung nach Anspruch 4, welche etwa 1 % bis etwa 20 % eines wasserlöslichen Polycarboxylatgerüststoffes enthält.
  6. Zusammensetzung nach Anspruch 5, worin der Polycarboxylatgerüststoff Citrat umfaßt.
  7. Zusammensetzung nach Anspruch 6, welche etwa 0,1 % bis etwa 1 % eines wasserlöslichen Salzes von Ethylendiamintetramethylenphosphonsäure, Diethylentriaminpentamethylenphosphonsäure, Ethylendiamintetraessigsäure oder Diethylentriaminpentaessigsäure enthält.
  8. Zusammensetzung nach Anspruch 1, welche etwa 30 % bis etwa 50 % des anionischen synthetischen grenzflächenaktiven Mittels und des Detergensgerüststoffes enthält.
  9. Zusammensetzung nach Anspruch 8, welche etwa 15 % bis etwa 30 % eines anionischen grenzflächenaktive Mittels enthält, welches ein C₁₀-C₁₈-Alkylsulfat, ein C₁₀-C₁₈-Alkylethoxysulfat mit im Durchschnitt bis zu etwa 4 Mol Ethylenoxid je Mol Alkylsulfat, ein lineares C₁₁-C₁₃-Alkylbenzolsulfonat oder Gemische hievon unfaßt.
  10. Zusammenstzung nach Anspruch 9, welche etwa 1 % bis etwa 20 % eines wasserlöslichen Polycarboxylatgerüststoffes enthält.
EP86200585A 1985-04-15 1986-04-07 Flüssige Reinigungsmittel mit einer anionischen oberflächenaktiven Verbindung, einem Verstärker und einem proteolytischen Enzym Expired EP0199404B1 (de)

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AT86200585T ATE77648T1 (de) 1985-04-15 1986-04-07 Fluessige reinigungsmittel mit einer anionischen oberflaechenaktiven verbindung, einem verstaerker und einem proteolytischen enzym.

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US723105 1991-06-28

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EP0199404A2 EP0199404A2 (de) 1986-10-29
EP0199404A3 EP0199404A3 (en) 1988-08-31
EP0199404B1 true EP0199404B1 (de) 1992-06-24

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EP86200585A Expired EP0199404B1 (de) 1985-04-15 1986-04-07 Flüssige Reinigungsmittel mit einer anionischen oberflächenaktiven Verbindung, einem Verstärker und einem proteolytischen Enzym

Country Status (5)

Country Link
EP (1) EP0199404B1 (de)
JP (1) JPS62595A (de)
AT (1) ATE77648T1 (de)
CA (1) CA1302924C (de)
DE (1) DE3685768T2 (de)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7262042B2 (en) 2001-12-20 2007-08-28 Henkel Kommanditgesellschaft Auf Aktien (Henkel Kgaa) Alkaline protease from Bacillus gibsonii (DSM 14393) and washing and cleaning products comprising said alkaline protease
US7449187B2 (en) 2001-12-20 2008-11-11 Henkel Kommanditgesellschaft Auf Aktien (Henkel Kgaa) Alkaline protease from Bacillus gibsonii (DSM 14391) and washing and cleaning products comprising said alkaline protease
US7569226B2 (en) 2001-12-22 2009-08-04 Henkel Kommanditgesellschaft Auf Aktien (Henkel Kgaa) Alkaline protease from Bacillus sp. (DSM 14392) and washing and cleaning products comprising said alkaline protease

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE68924654T2 (de) * 1988-01-07 1996-04-04 Novo Nordisk As Spezifische Protease.
JPH04202300A (ja) * 1990-11-29 1992-07-23 Shin Etsu Chem Co Ltd 洗浄剤組成物
US5466394A (en) * 1994-04-25 1995-11-14 The Procter & Gamble Co. Stable, aqueous laundry detergent composition having improved softening properties
DE59507049D1 (de) * 1995-03-01 1999-11-18 Weigert Chem Fab Reinigungsmittel für chirurgische Instrumente
DE10153792A1 (de) 2001-10-31 2003-05-22 Henkel Kgaa Neue Alkalische Protease-Varianten und Wasch- und Reinigungsmittel enthaltend diese neuen Alkalischen Protease-Varianten
DE10360805A1 (de) 2003-12-23 2005-07-28 Henkel Kgaa Neue Alkalische Protease und Wasch- und Reinigungsmittel, enthaltend diese neue Alkalische Protease
DE102004019751A1 (de) 2004-04-23 2005-11-17 Henkel Kgaa Neue Alkalische Proteasen und Wasch- und Reinigungsmittel, enthaltend diese neuen Alkalischen Proteasen
CA2589346A1 (en) 2004-12-09 2006-06-15 Dow Global Technologies Inc. Enzyme stabilization
EP1700907A1 (de) 2005-03-11 2006-09-13 Unilever N.V. Flüssige bleichmittelzusammensetzung
EP1700904A1 (de) 2005-03-11 2006-09-13 Unilever N.V. Flüssige Waschmittelzusammensetzung
DE102007029643A1 (de) 2006-09-08 2009-01-15 Henkel Ag & Co. Kgaa Reinigungsmittel
EP3075832B1 (de) 2015-03-30 2021-04-14 Dalli-Werke GmbH & Co. KG Mangan-aminosäure-verbindungen in reinigungszusammensetzungen
US11492572B2 (en) 2019-12-06 2022-11-08 Alene Candles LLC Effervescing compositions and tablets for treating toilets

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GR81415B (de) * 1983-02-14 1984-12-11 Procter & Gamble
IE81141B1 (en) * 1983-06-24 2000-04-05 Genencor Int Procaryotic carbonyl hydrolases
US4507219A (en) * 1983-08-12 1985-03-26 The Proctor & Gamble Company Stable liquid detergent compositions

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7262042B2 (en) 2001-12-20 2007-08-28 Henkel Kommanditgesellschaft Auf Aktien (Henkel Kgaa) Alkaline protease from Bacillus gibsonii (DSM 14393) and washing and cleaning products comprising said alkaline protease
US7449187B2 (en) 2001-12-20 2008-11-11 Henkel Kommanditgesellschaft Auf Aktien (Henkel Kgaa) Alkaline protease from Bacillus gibsonii (DSM 14391) and washing and cleaning products comprising said alkaline protease
US7569226B2 (en) 2001-12-22 2009-08-04 Henkel Kommanditgesellschaft Auf Aktien (Henkel Kgaa) Alkaline protease from Bacillus sp. (DSM 14392) and washing and cleaning products comprising said alkaline protease

Also Published As

Publication number Publication date
DE3685768T2 (de) 1993-01-21
DE3685768D1 (de) 1992-07-30
JPS62595A (ja) 1987-01-06
EP0199404A3 (en) 1988-08-31
ATE77648T1 (de) 1992-07-15
CA1302924C (en) 1992-06-09
EP0199404A2 (de) 1986-10-29

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