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
  • C11D3/38—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

• This invention relates to liquid detergent compositions containing enzymes. More specifically, this invention pertains to liquid detergent compositions containing a detersive surfactant, a proteolytic enzyme, a peptide aldehyde, and calcium ions. The combination of peptide aldehyde and calcium ions act to provide synergistic protease inhibitor benefits.
• protease-containing liquid aqueous detergents are well-known, especially in the context of laundry washing.
• a commonly encountered problem in such protease-containing liquid aqueous detergents is the degradation phenomenon by the proteolytic enzyme of second enzymes in the composition, such as amylase, lipase, and cellulase, or on the protease itself.
• second enzymes such as amylase, lipase, and cellulase
• peptide aldehydes are rather expensive and create complexities for the formulators, especially for liquid detergents.
• Other inhibitors such as calcium and boric acids are less expensive but do not stabilize enzymes as well as peptide aldehydes. It is thus an object of the present invention to provide a protease inhibitor system which is economical, effective and suitable for use in a liquid detergent composition.
• the present invention proposes to use a combination of calcium ions and peptide aldehydes as reversible protease inhibitors in aqueous liquid detergent compositions.
• the presence of both calcium and peptide aldehyde provides a synergistic stabilization of the protease.
• This novel combination provides the formulator added flexibility in designing a stabilization system.
• the levels of peptide aldehyde and calcium can be adjusted to deliver the most cost effective formula and to minimize product stability problems that often arise from the presence of divalent ions in a liquid detergent matrix.
• the present invention allows for the use of very low levels of peptide aldehydes in the liquid detergent compositions herein. This is particularly critical in the formulation of relatively inexpensive, concentrated liquid detergent compositions which are encompassed by the present invention.
• Another advantage of the present invention is that even enzymes which are highly sensitive to proteolytic degradation can now be incorporated in liquid detergent compositions comprising a protease. Moreover, it has also been discovered that the increased stability of the protease enzyme allows for improved skincare benefits. These benefits include softening of the skin and hands and less drying from exposure of the hands to the dishwashing liquor.
• EP 293 881 discloses the use of peptide boronic acids as inhibitors of trypsin-like serine proteases.
• EP 185 390 and US 4,399,065 disclose the use of certain peptide aldehydes derivatives for the inhibition of blood coagulation.
• J 90029670 discloses the use of optically active alpha amino aldehydes for the inhibition of enzymes in general. See also "Inhibition of
• the invention herein is a liquid detergent composition
• a liquid detergent composition comprising: a) an effective amount of a detersive surfactant; b) an active proteolytic enzyme; c) a source of calcium ions; and d) a peptide aldehyde having the formula:
• the proteolytic enzyme useful herein is preferably a subtilisin-type protease and may be selected from the group consisting of Alcalase®, Subtilisin BPN', Protease A, Protease B, and mixtures thereof.
• the source of calcium ion for use herein is preferably selected from calcium formate, calcium xylene sulfonate, calcium chloride, calcium acetate, calcium sulfate. and mixtures thereof.
• compositions herein may contain further detersive adjuncts, including but not limited to, one or more of the following: suds boosters, builders, soil release polymers, polyacrylate polymers, dispersing agents, dye transfer inhibitors, dyes, perfumes, processing aids, brighteners, and mixtures thereof.
• the detersive surfactant is typically present in an amount of from about 10% to about 70%, by weight of total composition.
• the laundry compositions may optionally comprise an effective amount of a source of boric acid and a diol.
• an “effective amount” or “stain removal-improving amount” is any amount capable of measurably improving soil cleaning or stain removal from a substrate, i.e., soiled fabric or soiled dishware, when it is washed by the consumer. In general, this amount may vary quite widely.
• the liquid aqueous detergent compositions according to the present invention comprise four essential ingredients: (A) a peptide aldehyde or a mixture thereof, (B) a proteolytic enzyme or a mixture thereof, (C) a detersive surfactant, and (D) calcium ion.
• the compositions according to the present invention preferably further comprise (E) a detergent-compatible second enzyme or a mixture thereof, and may further comprise (F) other optional ingredients.
• Peptide aldehydes - The detergent compositions according to the present invention comprise, as a first essential ingredient, a peptide aldehyde having the formula:
• Z is an N-capping moiety selected from the group consisting of phosphoramidate [(R"O) 2 (O)P-], sulfenamide [(SR") 2 -], sulfonamide [(R"(O)2S-], sulfonic acid
• each R" is independently selected from the group consisting of straight or branched C ⁇ -C unsubstituted alkyl, phenyl, C7-C9 alkylaryl, and cycloalkyl moieties, wherein the cycloalkyl ring may span C4-C8 and may contain one or more heteroatoms selected from the group consisting of O,N,and S (preferred R" is selected from the group consisting of methyl, ethyl, and
• R moieties are selected from the group consisting of methyl, iso- propyl, sec-butyl, iso-butyl, -C6H5, -CH2-C6H5, and -CH2CH2-C6H5, which respectively may be derived from the amino acids Ala, Val, He, Leu, PGly (phenylglycine), Phe, and HPhe (homophenylalanine) by converting the carboxylic acid group to an aldehyde group.
• Preferred B peptide chains are selected from the group consisting of peptide chains having the amino acid sequences according to the general formula:
• A- is selected from Ala, Gly;
• a 2 if present, is selected from Val, Ala, Gly, He;
• A-- if present, is selected from Phe, Leu, Val, He;
• a 4 if present, is any amino acid, but preferably is selected from Gly, Ala;
• A-5 if present, is any amino acid, but preferably is Gly, Ala, Lys.
• the present invention aldehydes may be prepared from the corresponding amino acid whereby the C-terminal end of said amino acid is converted from a carboxylic group to an aldehyde group.
• Such aldehydes may be prepared by known processes, for instance as described in US 5015627, EP 185 930, EP 583.534, and DE 32 00 812.
• the peptide aldehydes according to the present invention bind to the proteolytic enzyme in the liquid detergent composition, thereby inhibiting said proteolytic enzyme. Upon dilution in water, the proteolytic activity is restored by dissociation of the proteolytic enzyme/peptide aldehyde complex.
• N-terminal end of said protease inhibitors according to the present invention is protected by one of the N-capping moiety protecting groups selected from the group consisting of carbamates, ureas, sulfonamides, phosphonamides,thioureas, sulfenamides, sulfonic acids, phosphinamides, thiocarbamates, amidophosphates, and phosphonamides.
• the N-terminal end of said protease inhibitor is protected by a methyl, ethyl or benzyl carbamate [CH3 ⁇ -(O)C-; CH3CH 2 O-(O)C-; or C6H5CH2 ⁇ -(O)C-], methyl, ethyl or benzyl urea [CH3NH- (O)C-; CH 3 CH 2 NH-(O)C-; or C6H 5 CH NH-(O)C-], methyl, ethyl or benzyl sulfonamide [CH3SO2-; CH3CH2SO2-; or C6H5CH2SO2-], and methyl, ethyl or benzyl amidophosphate [CH3 ⁇ (OH)(O)P-; CH3CH 2 O(OH)(O)P-; or C 6 H 5 CH 2 O(OH)(O)P-] groups.
• N-Ms-Phe-Gly-Ala-LeuH A solution is prepared by adding 0.337 g (0.798 mmol) Dess-Martin periodinane to 5 ml CH2CI2 and stirring for 10 minutes. To this solution 0.125 g (0.266 mmol) N-Ms-Phe-Gly-Ala-Leucinol is added in one portion. The reaction is continued until TLC showed complete conversion at which time the solution is poured into 25 ml sat'd NaHCO3 containing 1.8 g (5.586 mmol) Na2S2 ⁇ 3- After stirring for 10 minutes the mixture is extracted with EtOAc (3X, 50 ml). The combined extracts are dried (MgSO4), evaporated, and chromatographed on silica to afford 0.048 g of the product.
• Moc-Leu-OH-L-Leucine (5.0 g, 38.2 mmol) is dissolved in 38 ml IN NaOH and cooled to 0°C.
• Methyl chloroformate (3.1 ml, 40.0 mmol) is added dropwise while in a separate addition funnel IN NaOH is added as to maintain pH at 9.0-9.5.
• Moc-Leu-LeuH-A solution containing 4.4 g (10.41 mmol) Dess-Martin periodinane suspended in 100 ml CH2CI2 is prepared and stirred for 10 minutes.
• 1.0 g (3.47 mmol) Moc-Leu-Leucinol is added and the solution stirred 2 h at room temperature followed by pouring into 100 ml of saturated NaHCO3 containing 18 g (72.87 mmol) Na2S2 ⁇ 3. This solution is stirred 10 minutes and then extracted with EtOAc (2X, 125ml), dried (MgSO4) and the solvent evaporated. Chromatography on silica affords 0.550 g of pure product.
• Moc-Phe-Gly-Ala-Leu-OMe - Z-Gly-Ala-Leu-OMe (29.0 g, 0.071 M) is dissolved in 300 ml MeOH and 35 ml 4.0 M HCl in dioxane. To this solvent mixture is added 5.8 g of 10% Pd/C portionwise. The slurry is degassed with an aspirator and H2 introduced via balloon. The slurry is maintained under a positive pressure of H2 and stirred overnight. The slurry is filtered through Celite and a sintered glass funnel and washed thoroughly with MeOH. The solvent is removed and the residue is triturated with ether. The slurry is filtered and the filter cake dried under vacuum.
• Moc-Phe-Gly-Ala-Leucinol - Moc-Phe-Gly-Ala-Leu-OMe (21.3 g, 44.5 mmol) is dissolved in a mixture of 400 ml EtOH and 250 ml THF. The solution is cooled to 0°C and 9.88 g (89.0 mmol) CaCl2 is added. In 5 min the slurry will be homogenized and 6.73 g (178.0 mmol) NaBH4 added portionwise over a period of 5 min. The solution is stirred at 0°C for 2 hours and the reaction carefully quenched with IN HCl. The EtOH and THF are removed under vacuum and the remaining aqueous mixture extracted with 500 ml EtOAc.
• Esperase® Savinase® (Copenhagen, Denmark), Gist-brocades' Maxatase®, Maxacal® and Maxapem 15® (protein engineered Maxacal®) (Delft, Netherlands), and subtilisin BPN and BPN'(preferred), which are commercially available.
• Preferred proteolytic enzymes are also modified bacterial serine proteases, such as those made by Genencor International, Inc.(San Francisco, California) which are described in European Patent 251,446, filed April 28, 1987 (particularly pages 17, 24 and 98), and which is called herein "Protease B", and U.S.
• Protease A a modified bacterial serine proteolytic enzyme
• BPN' modified bacterial serine proteolytic enzyme
• Preferred proteolytic enzymes are selected from the group consisting of Alcalase ® (Novo Industri A/S), BPN', Protease A and Protease B (Genencor), and mixtures thereof. Protease B is most preferred.
• protease D is a carbonyl hydrolase variant having an amino acid sequence not found in nature, which is derived from a precursor carbonyl hydrolase by substituting a different amino acid for a plurality of amino acid residues at a position in said carbonyl hydrolase equivalent to position +76, preferably also in combination with one or more amino acid residue positions equivalent to those selected from the group consisting of +99, +101, +103, +104, +107, +123, +27, +105, +109, +126, +128, +135, +156, +166, +195, +197, +204, +206, +210, +216, +217, +218, +222, +260, +265, and/or +274 according to the numbering of Bacillus amyloliquefaciens subtilisin, as described in WO 95/10615 published April 20, 1995 by Genencor International.
• proteases are also described in PCT publications: WO 95/30010 published Novenber 9, 1995 by The Procter & Gamble Company; WO 95/3001 1 published Novenber 9, 1995 by The Procter & Gamble Company; WO 95/29979 published Novenber 9, 1995 by The Procter & Gamble Company.
• the calcium useful herein is enzyme-accessible. Therefore, the claimed compositions are substantially free of sequestrants, for example, polyacids capable of forming calcium complexes which are soluble in the composition. However, minor amounts of sequestrants such as polyacids or mixtures of polyacids can be used.
• the enzyme-accessible calcium is defined as the amount of calcium-ions effectively available to the enzyme component. From a practical standpoint the enzyme-accessible calcium is therefore the soluble calcium in the composition in the absence of any storage sequestrants, e.g., having an equilibrium constant of complexation with calcium equal to or greater than 1.5 at 20°C.
• Detersive Surfactant An effective amount, typically from about 1 to 95, preferably about 8 to 70, weight %, of detersive surfactant is yet another essential ingredient in the present invention.
• the detersive surfactant can be selected from the group consisting of anionics, nonionics, cationics, ampholytics, zwitterionics, and mixtures thereof.
• the present detergent compositions can be formulated to be used in the context of laundry cleaning or in other different cleaning applications, particularly including dishwashing. The particular surfactants used can therefore vary widely depending upon the particular end-use envisioned.
• R 3 is Cjo-Cig alkyl
• R 4 is methyl, ethyl or isopropyl.
• methyl ester sulfonates wherein R 3 is C14-C- 6 alkyl.
• Alkyl sulfate surfactants are another type of anionic surfactant of importance for use herein.
• R preferably is a C - 0-C24 hydrocarbyl, preferably an alkyl or hydroxyalkyl having a C- Q-C20 alkyl component, more preferably a Cj2- C] alkyl or hydroxyalkyl
• M is H or a cation, e.g., an alkali metal cation (e.g., sodium, potassium, lithium), substituted or unsubstituted ammonium cations such as methyl-, dimethyl-, and trimethyl ammonium and quaternary ammonium cations, e.g., tetramethyl-ammonium and dimethyl pipe
• Exemplary surfactants are C ⁇ -Cjg alkyl polyethoxylate (1.0) sulfate, C ⁇ -C- g alkyl polyethoxylate (2.25) sulfate, C12-C1 alkyl polyethoxylate (3.0) sulfate, and C * 2-C * 8 alkyl polyethoxylate (4.0) sulfate wherein M is conveniently selected from sodium and potassium.
• the condensation products of aliphatic alcohols with from about 1 to about 25 moles of ethylene oxide can either be straight or branched, primary or secondary, and generally contains from about 8 to about 22 carbon atoms. Particularly preferred are the condensation products of alcohols having an alkyl group containing from about 10 to about 20 carbon atoms with from about 2 to about 18 moles of ethylene oxide per mole of alcohol.
• the condensation products of ethylene oxide with the product resulting from the reaction of propylene oxide and ethylenediamine consist of the reaction product of ethylenediamine and excess propylene oxide, and generally has a molecular weight of from about 2500 to about 3000.
• This hydrophobic moiety is condensed with ethylene oxide to the extent that the condensation product contains from about 40% to about 80% by weight of polyoxyethylene and has a molecular weight of from about 5,000 to about 1 1 ,000.
• Examples of this type of nonionic surfactant include certain of the commercially available Tetronic® compounds, marketed by BASF.
• Semi-polar nonionic surfactants are a special category of nonionic surfactants which include water-soluble amine oxides containing one alkyl moiety of from about 10 to about 18 carbon atoms and 2 moieties selected from the group consisting of alkyl groups and hydroxyalkyl groups containing from about 1 to about 3 carbon atoms; water-soluble phosphine oxides containing one alkyl moiety of from about 10 to about 18 carbon atoms and 2 moieties selected from the group consisting of alkyl groups and hydroxyalkyl groups containing from about 1 to about 3 carbon atoms; and water-soluble sulfoxides containing one alkyl moiety of from about 10 to about 18 carbon atoms and a moiety selected from the group consisting of alkyl and hydroxyalkyl moieties of from about 1 to about 3 carbon atoms.
• R 3 ( OR 4 ) ⁇ N ( R 5 ) 2
• R 3 is an alkyl, hydroxyalkyl, or alkyl phenyl group or mixtures thereof containing from about 8 to about 22 carbon atoms
• R 4 is an alkylene or hydroxyalkylene group containing from about 2 to about 3 carbon atoms or mixtures thereof
• x is from 0 to about 3
• each R-5 is an alkyl or hydroxyalkyl group containing from about 1 to about 3 carbon atoms or a polyethylene oxide group containing from about 1 to about 3 ethylene oxide groups.
• the R-5 groups can be attached to each other, e.g., through an oxygen or nitrogen atom, to form a ring structure.
• amine oxide surfactants in particular include Cin-C * 8 alkyl dimethyl amine oxides and Cg-C* 2 alkoxy ethyl dihydroxy ethyl amine oxides.
• hydrophobic group containing from about 6 to about 30 carbon atoms, preferably from about 10 to about 16 carbon atoms and a polysaccharide, e.g., a polyglycoside, hydrophilic group containing from about 1.3 to about 10, preferably from about 1.3 to about 3, most preferably from about 1.3 to about 2.7 saccharide units.
• Any reducing saccharide containing 5 or 6 carbon atoms can be used, e.g., glucose, galactose and galactosyl moieties can be substituted for the glucosyl moieties.
• the hydrophobic group is attached at the 2-, 3-, 4-, etc.
• a polyalkylene-oxide chain joining the hydrophobic moiety and the polysaccharide moiety.
• the preferred alkyleneoxide is ethylene oxide.
• Typical hydrophobic groups include alkyl groups, either saturated or unsaturated, branched or unbranched containing from about 8 to about 18, preferably from about 10 to about 16, carbon atoms.
• the alkyl group is a straight chain saturated alkyl group.
• the alkyl group can contain up to about 3 hydroxy groups and/or the polyalkyleneoxide chain can contain up to about 10, preferably less than 5, alkyleneoxide moieties.
• Suitable mixtures include coconut alkyl, di-, tri-, tetra-, and pentaglucosides and tallow alkyl tetra-, penta-, and hexa-glucosides.
• the preferred alkylpolyglycosides have the formula
• R2 ⁇ (C n H 2n O)t(glycosyl) x
• R 2 is selected from the group consisting of alkyl, alkyl-phenyl, hydroxyalkyl, hydroxyalkylphenyl, and mixtures thereof in which the alkyl groups contain from about 10 to about 18, preferably from about 12 to about 14, carbon atoms; n is 2 or 3, preferably 2; t is from 0 to about 10, preferably 0; and x is from about 1.3 to about 10, preferably from about 1.3 to about 3, most preferably from about 1.3 to about 2.7.
• the glycosyl is preferably derived from glucose.
• the alcohol or alkylpolyethoxy alcohol is formed first and then reacted with glucose, or a source of glucose, to form the glucoside (attachment at the 1 -position).
• the additional glycosyl units can then be attached between their 1- position and the preceding glycosyl units 2-, 3-, 4- and/or 6-position, preferably predominantly the 2-position.
• Fatty acid amide surfactants having the formula: o
• R 6 -C-N ( R 7 ) 2 wherein R ⁇ is an alkyl group containing from about 7 to about 21 (preferably from about 9 to about 17) carbon atoms and each R? is selected from the group consisting of hydrogen, C1-C4 alkyl, C1-C4 hydroxyalkyl, and -(C 2 H4 ⁇ ) x H where x varies from about 1 to about 3.
• amides are C -C20 ammonia amides, monoethanolamides, diethanolamides, and isopropanolamides.
• Cationic Surfactants - Cationic detersive surfactants can also be included in detergent compositions of the present invention.
• Cationic surfactants include the ammonium surfactants such as alkyldimethylammonium halogenides, and those surfactants having the formula:
• R 2 is an alkyl or alkyl benzyl group having from about 8 to about 18 carbon atoms in the alkyl chain
• each R 3 is selected from the group consisting of -CH2CH2- , -CH 2 CH(CH3)-, -CH 2 CH(CH 2 OH)-, -CH2CH 2 CH 2 -, and mixtures thereof
• each R 4 is selected from the group consisting of C1-C4 alkyl, C- -C4 hydroxyalkyl, benzyl, ring structures formed by joining the two R 4 groups, - CH2CHOHCHOHCOR 6 CHOH-CH 2 OH wherein R 6 is any hexose or hexose polymer having a molecular weight less than about 1000, and hydrogen when y is not O
• R-5 is the same as R 4 or is an alkyl chain wherein the total number of
• Surfactants - Ampholytic surfactants can be incorporated into the detergent compositions hereof. These surfactants can be broadly described as aliphatic derivatives of secondary or tertiary amines, or aliphatic derivatives of heterocyclic secondary and tertiary amines in which the aliphatic radical can be straight chain or branched.
• One of the aliphatic substituents contains at least about 8 carbon atoms, typically from about 8 to about 18 carbon atoms, and at least one contains an anionic water-solubilizing group, e.g., carboxy, sulfonate, sulfate. See U.S. Patent No. 3,929,678 to Laughlin et al., issued December 30, 1975 at column 19, lines 18-35 for examples of ampholytic surfactants.
• Zwitterionic surfactants can also be incorporated into the detergent compositions hereof. These surfactants can be broadly described as derivatives of secondary and tertiary amines, derivatives of heterocyclic secondary and tertiary amines, or derivatives of quaternary ammonium, quaternary phosphonium or tertiary sulfonium compounds. See U.S. Patent No. 3,929,678 to Laughlin et al., issued December 30, 1975 at column 19, line 38 through column 22, line 48 for examples of zwitterionic surfactants. Ampholytic and zwitterionic surfactants are generally used in combination with one or more anionic and/or nonionic surfactants.
• the liquid detergent compositions hereof may also contain an enzyme-enhancing amount of polyhydroxy fatty acid amide surfactant.
• enzyme-enhancing is meant that the formulator of the composition can select an amount of polyhydroxy fatty acid amide to be incorporated into the compositions that will improve enzyme cleaning performance of the detergent composition. In general, for conventional levels of enzyme, the incorporation of about 1%, by weight, polyhydroxy fatty acid amide will enhance enzyme performance.
• the detergent compositions herein will typically comprise about 1% weight basis, polyhydroxy fatty acid amide surfactant, preferably from about 3% to about 30%, of the polyhydroxy fatty acid amide.
• the polyhydroxy fatty acid amide surfactant component comprises compounds of the structural formula:
• R* is H, C1-C4 hydrocarbyl, 2-hydroxy ethyl, 2-hydroxy propyl, or a mixture thereof, preferably C 1-C4 alkyl, more preferably C ⁇ or C2 alkyl, most preferably C ⁇ alkyl (i.e., methyl); and R 2 is a C5-C31 hydrocarbyl, preferably straight chain C7-C19 alkyl or alkenyl, more preferably straight chain C9-C17 alkyl or alkenyl, most preferably straight chain C ⁇ ⁇ -C ⁇ 5 alkyl or alkenyl, or mixtures thereof; and Z is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyls directly connected to the chain, or an alkoxylated derivative (preferably ethoxylated or propoxylated) thereof.
• Z preferably will be derived from a reducing sugar in a reductive amination reaction; more preferably Z will be a glycityl.
• Suitable reducing sugars include glucose, fructose, maltose, lactose, galactose, mannose, and xylose.
• high dextrose corn syrup, high fructose corn syrup, and high maltose corn syrup can be utilized as well as the individual sugars listed above. These corn syrups may yield a mix of sugar components for Z. It should be understood that it is by no means intended to exclude other suitable raw materials.
• Z preferably will be selected from the group consisting of -CH 2 -(CHOH) n -CH 2 OH, -CH(CH2 ⁇ H)-(CHOH) n _-, -CH2 ⁇ H, -CH - (CHOH)2(CHOR')(CHOH)-CH2OH, and alkoxylated derivatives thereof, where n is an integer from 3 to 5, inclusive, and R' is H or a cyclic or aliphatic monosaccharide. Most preferred are glycityls wherein n is 4, particularly -CH2-(CHOH)4-CH2OH.
• R' can be, for example, N-methyl, N-ethyl, N-propyl, N-isopropyl, N-butyl, N- 2-hydroxy ethyl, or N-2-hydroxy propyl.
• R2-CO-N ⁇ can be, for example, cocamide, stearamide, oleamide, lauramide, myristamide, capricamide, palmitamide, tallowamide, etc.
• Z can be 1-deoxyglucityl, 2-deoxyfructityl, 1-deoxymaltityl, 1 -deoxylactityl, 1- deoxygalactityl, 1-deoxymannityl, 1-deoxymaltotriotityl, etc.
• polyhydroxy fatty acid amides are known in the art. In general, they can be made by reacting an alkyl amine with a reducing sugar in a reductive amination reaction to form a corresponding N-alkyl polyhydroxyamine, and then reacting the N-alkyl polyhydroxyamine with a fatty aliphatic ester or triglyceride in a condensation/amidation step to form the N-alkyl, N-polyhydroxy fatty acid amide product.
• Processes for making compositions containing polyhydroxy fatty acid amides are disclosed, for example, in G.B. Patent
• Second Enzyme - Preferred compositions herein further comprise a performance-enhancing amount of a detergent-compatible second enzyme.
• detergent-compatible is meant compatibility with the other ingredients of a liquid detergent composition, such as detersive surfactant and detergency builder.
• second enzymes are preferably selected from the group consisting of lipase, amylase, cellulase, and mixtures thereof.
• second enzyme excludes the proteolytic enzymes discussed above, so each composition which has a second enzyme contains at least two kinds of enzyme, including at least one proteolytic enzyme. The amount of second enzyme used in the composition varies according to the type of enzyme.
• weight % of these second enzymes are preferably used.
• Mixtures of the same class of enzymes (e.g. lipase) or two or more classes (e.g. cellulase and lipase) may be used.
• Purified or non-purified forms of the enzyme may be used.
• Any lipolytic enzyme suitable for use in a liquid detergent composition can be used in these compositions.
• Suitable lipase enzymes for use herein include those of bacterial and fungal origin.
• Suitable bacterial Upases include those produced by microorganisms of the Pseudomonas groups, such as Pseudomonas stutzeri ATCC 19.154, as disclosed in British Patent 1,372,034, incorporated herein by reference. Suitable upases include those which show a positive immunological cross-reaction with the antibody of the lipase produced by the microorganism Pseudomonas fluorescens IAM 1057. This lipase and a method for its purification have been described in Japanese Patent Application 53-20487, laid open on February 24, 1978. This lipase is available from Amano Pharmaceutical Co.
• Amano-P Lipase P
• Such Upases should show a positive immunological cross-reaction with the Amano-P antibody, using the standard and well-known immunodiffusion procedure according to Ouchterlony (Acta. Med. Scan., 133, pages 76-79 (1950)).
• Ouchterlony Acta. Med. Scan., 133, pages 76-79 (1950)
• These Upases, and a method for their immunological cross-reaction with Amano-P are also described in U.S. Patent 4,707,291, Thorn et al., issued November 17, 1987, incorporated herein by reference.
• Typical examples thereof are the Amano-P lipase, the lipase ex Pseudomonas fragi FERM P 1339 (available under the trade name Amano-B), lipase ex Pseudomonas nitroreducens var. lipolvticum FERM P 1338 (available under the trade name Amano-CES), Upases ex Chromobacter viscosum. e.g. Chro obacter viscosum var. lipolvticum NRRLB 3673, commercially available from Toyo Jozo Co., Tagata. Japan; and further Chromobacter viscosum Upases from U.S. Biochemical Corp., U.S.A. and Disoynth Co., The Netherlands, and Upases ex Pseudomonas gladioli.
• Amano-P lipase the lipase ex Pseudomonas fragi FERM P 1339 (available under the trade name Aman
• Suitable fungal Upases include those producible by Humicola lanuginosa and Thermomvces lanuginosus. Most preferred is lipase obtained by cloning the gene from Humicola lanuginosa and expressing the gene in Aspergillus oryzae as described in European Patent Application 0 258 068 (Novo Industri A/S), commercially available from Novo Nordisk A/S under the trade name Lipolase®. From about 10 to 18,000, preferably about 60 to 6,000, lipase units per gram (LU/g) of lipase can be used in these compositions.
• Lipolase® From about 10 to 18,000, preferably about 60 to 6,000, lipase units per gram (LU/g) of lipase can be used in these compositions.
• a lipase unit is that amount of lipase which produces 1 mmol of titratable fatty acid per minute in a pH stat, where pH is 9.0, temperature is 30°C, substrate is an emulsion of 3.3wt % of olive oil and 3.3% gum arabic, in the presence of 13 mmol/1 Ca and 20 mmol/1 NaCl in 5 mmol/1 Tris-buffer.
• Any cellulase suitable for use in a liquid detergent composition can be used in these compositions.
• Suitable cellulase enzymes for use herein include those from bacterial and fungal origins. Preferably, they will have a pH optimum of between 5 and 9.5. From about 0.0001 to 0.1 weight % cellulase can be used.
• Suitable cellulases are disclosed in U.S. Patent 4,435,307, Barbesgaard et al., issued March 6, 1984, incorporated herein by reference, which discloses fungal cellulase produced from Humicola insolens. Suitable cellulases are also disclosed in GB-A-2.075.028, GB-A-2.095.275 and DE-OS-2.247.832.
• cellulases examples include cellulases produced by a strain of Humicola insolens (Humicola grisea var. thermoidea), particularly the Humicola strain DSM 1800, and cellulases produced by a fungus of Bacillus N or a cellulase 212- producing fungus belonging to the genus Aeromonas. and cellulase extracted from the hepatopancreas of a marine mollusc (Dolabella Auricula Solander).
• Humicola insolens Haicola grisea var. thermoidea
• DSM 1800 cellulases produced by a fungus of Bacillus N or a cellulase 212- producing fungus belonging to the genus Aeromonas.
• cellulase extracted from the hepatopancreas of a marine mollusc Dolabella Auricula Solander.
• Amylases include, for example, amylases obtained from a special strain of B. licheniformis, described in more detail in British Patent
• Amylolytic proteins include, for example,
• amylase From about 0.0001% to 0.55, preferably 0.0005 to 0.1, wt. % amylase can be used.
• Optional Ingredients - Detergent builders can optionally be included in the compositions herein, especially for laundry compositions.
• Inorganic as well as organic builders can be used.
• the compositions will typically comprise at least about 1% builder and can be either an inorganic or organic builder.
• Liquid laundry formulations preferably comprise from about 3% to 30%, more preferably about 5 to 20%, by weight, of detergent builder.
• Inorganic detergent builders include, but are not limited to, the alkali metal, ammonium and alkanolammonium salts of polyphosphates (exemplified by the tripolyphosphates, pyrophosphates, and glassy polymeric meta-phosphates), phosphonates, phytic acid, silicates, carbonates (including bicarbonates and sesquicarbonates), sulphates, and aluminosilicates.
• Borate builders, as well as builders containing borate-forming materials that can produce borate under detergent storage or wash conditions hereinafter, collectively “borate builders"
• non-borate builders are used in the compositions of the invention intended for use at wash conditions less than about 50°C, especially less than about 40°C.
• silicate builders are the alkali metal silicates, particularly those having a SiO2:Na2O ratio in the range 1.6: 1 to 3.2: 1 and layered silicates, such as the layered sodium silicates described in U.S. Patent 4,664,839, issued May 12, 1987 to H. P. Rieck, incorporated herein by reference.
• other silicates may also be useful such as for example magnesium silicate, which can serve as a crispening agent in granular formulations, as a stabilizing agent for oxygen bleaches, and as a component of suds control systems.
• carbonate builders are the alkaline earth and alkali metal carbonates, including sodium carbonate and sesquicarbonate and mixtures thereof with ultra- fine calcium carbonate as disclosed in German Patent Application No. 2,321,001 published on November 15, 1973, the disclosure of which is incorporated herein by reference.
• Aluminosilicate builders are useful in the present invention. Aluminosilicate builders are of great importance in most currently marketed heavy duty granular detergent compositions, and can also be a significant builder ingredient in liquid detergent formulations. Aluminosilicate builders include those having the empirical formula:
• Preferred alumino-silicates are zeolite builders which have the formula:
• aluminosilicate ion exchange materials are commercially available. These aluminosilicates can be crystalline or amorphous in structure and can be naturally-occurring aluminosilicates or synthetically derived. A method for producing aluminosilicate ion exchange materials is disclosed in U.S. Patent 3,985,669, Krummel, et al., issued October 12, 1976, incorporated herein by reference. Preferred synthetic crystalline aluminosilicate ion exchange materials useful herein are available under the designations Zeolite A, Zeolite P (B), and Zeolite X. In an especially preferred embodiment, the crystalline aluminosilicate ion exchange material has the formula:
• the aluminosilicate has a particle size of about 0.1-10 microns in diameter.
• polyphosphates are the alkali metal tripolyphosphates, sodium, potassium and ammonium pyrophosphate, sodium and potassium and ammonium pyrophosphate, sodium and potassium orthophosphate, sodium polymeta phosphate in which the degree of polymerization ranges from about 6 to about 21, and salts of phytic acid.
• Examples of phosphonate builder salts are the water-soluble salts of ethane 1- hydroxy- 1 , 1 -diphosphonate particularly the sodium and potassium salts, the water- soluble salts of methylene diphosphonic acid e.g. the trisodium and tripotassium salts and the water-soluble salts of substituted methylene diphosphonic acids, such as the trisodium and tripotassium ethylidene, isopyropylidene benzylmethylidene and halo methylidene phosphonates.
• Phosphonate builder salts of the aforementioned types are disclosed in U.S. Patent Nos.
• Organic detergent builders preferred for the purposes of the present invention include a wide variety of polycarboxylate compounds.
• polycarboxylate refers to compounds having a plurality of carboxylate groups, preferably at least 3 carboxylates.
• Polycarboxylate builder can generally be added to the composition in acid form, but can also be added in the form of a neutralized salt.
• alkali metals such as sodium, potassium, and lithium, or alkanolammonium salts are preferred.
• polycarboxylate builders include a variety of categories of useful materials.
• One important category of polycarboxylate builders encompasses the ether polycarboxylates.
• a number of ether polycarboxylates have been disclosed for use as detergent builders.
• Examples of useful ether polycarboxylates include oxydisuccinate, as disclosed in Berg, U.S. Patent 3,128,287, issued April 7, 1964, and Lamberti et al., U.S. Patent 3,635,830, issued January 18, 1972, both of which are incorporated herein by reference.
• a specific type of ether polycarboxylates useful as builders in the present invention also include those having the general formula:
• A is H or OH; B is H or -O-CH(COOX)-CH 2 (COOX); and X is H or a salt- forming cation.
• a and B are both H, then the compound is oxydissuccinic acid and its water-soluble salts. If A is OH and B is H, then the compound is tartrate monosuccinic acid (TMS) and its water-soluble salts.
• TDS tartrate disuccinic acid
• Suitable ether polycarboxylates also include cyclic compounds, particularly alicyclic compounds, such as those described in U.S. Patents 3,923,679; 3,835,163; 4,158,635; 4,120,874 and 4,102,903, all of which are incorporated herein by reference.
• Other useful detergency builders include the ether hydroxypolycarboxylates represented by the structure:
• n is from about 2 to about 15 (preferably n is from about 2 to about 10, more preferably n averages from about 2 to about 4) and each R is the same or different and selected from hydrogen, C * _4 alkyl or C 1.4 substituted alkyl (preferably R is hydrogen).
• Still other ether polycarboxylates include copolymers of maleic anhydride with ethylene or vinyl methyl ether, 1, 3, 5-trihydroxy benzene-2, 4, 6-trisulphonic acid, and carboxymethyloxysuccinic acid.
• Organic polycarboxylate builders also include the various alkali metal, ammonium and substituted ammonium salts of polyacetic acids. Examples include the sodium, potassium, lithium, ammonium and substituted ammonium salts of ethylenediamine tetraacetic acid, and nitrilotriacetic acid. Also included are polycarboxylates such as mellitic acid, succinic acid, oxydisuccinic acid, polymaleic acid, benzene 1,3,5-tricarboxylic acid, and carboxymethyloxysuccinic acid, and soluble salts thereof.
• polycarboxylates such as mellitic acid, succinic acid, oxydisuccinic acid, polymaleic acid, benzene 1,3,5-tricarboxylic acid, and carboxymethyloxysuccinic acid, and soluble salts thereof.
• Citrate builders e.g., citric acid and soluble salts thereof (particularly sodium salt), are polycarboxylate builders of particular importance for heavy duty liquid detergent formulations, but can also be used in granular compositions.
• Other carboxylate builders include the carboxylated carbohydrates disclosed in U.S. Patent 3,723,322, Diehl, issued March 28, 1973, incorporated herein by reference.
• Also suitable in the detergent compositions of the present invention are the 3,3- dicarboxy-4-oxa-l,6-hexanedioates and the related compounds disclosed in U.S. Patent 4,566,984, Bush, issued January 28, 1986, incorporated herein by reference.
• Useful succinic acid builders include the C5-C20 alkyl succinic acids and salts thereof.
• a particularly preferred compound of this type is dodecenylsuccinic acid.
• Alkyl succinic acids typically are of the general formula R-CH(COOH)CH2(COOH) i.e., derivatives of succinic acid, wherein R is hydrocarbon, e.g., C * 0-C20 alkyl or alkenyl, preferably Ci2-Cj6 or wherein R may be substituted with hydroxyl, sulfo, sulfoxy or sulfone substituents, all as described in the above-mentioned patents.
• R is hydrocarbon, e.g., C * 0-C20 alkyl or alkenyl, preferably Ci2-Cj6 or wherein R may be substituted with hydroxyl, sulfo, sulfoxy or sulfone substituents, all as described in the above-mentioned patents.
• the succinate builders are preferably used in the form of their water-soluble salts, including the sodium, potassium, ammonium and alkanolammonium salts.
• Specific examples of succinate builders include: laurylsuccinate, myristylsuccinate, palmitylsuccinate, 2-dodecenylsuccinate (preferred), 2- pentadecenylsuccinate, and the like. Laurylsuccinates are the preferred builders of this group, and are described in European Patent Application 86200690.5/0.200,263, published November 5, 1986.
• useful builders also include sodium and potassium carboxymethyloxymalonate, carboxymethyloxysuccinate, cis-cyclo-hexane- hexacarboxylate, cis-cyclopentane-tetracarboxylate, water-soluble polyacrylates (these polyacrylates having molecular weights to above about 2,000 can also be effectively utilized as dispersants), and the copolymers of maleic anhydride with vinyl methyl ether or ethylene.
• polycarboxylates are the polyacetal carboxylates disclosed in U.S. Patent 4,144,226, Crutchfield et al., issued March 13, 1979, incorporated herein by reference. These polyacetal carboxylates can be prepared by bringing together, under polymerization conditions, an ester of glyoxylic acid and a polymerization initiator. The resulting polyacetal carboxylate ester is then attached to chemically stable end groups to stabilize the polyacetal carboxylate against rapid depolymerization in alkaline solution, converted to the corresponding salt, and added to a surfactant.
• Polycarboxylate builders are also disclosed in U.S. Patent 3,308,067, Diehl, issued March 7, 1967, incorporated herein by reference. Such materials include the water-soluble salts of homo- and copolymers of aliphatic carboxylic acids such as maleic acid, itaconic acid and methylenemalonic acid.
• organic builders known in the art can also be used.
• monocarboxylic acids, and soluble salts thereof, having long chain hydrocarbyls can be utilized. These would include materials generally referred to as "soaps.” Chain lengths of C 10-C20 are typically utilized.
• the hydrocarbyls can be saturated or unsaturated.
• soil release agents include soil release agents, chelating agents, clay soil removal/anti redeposition agents, polymeric dispersing agents, bleaches, brighteners, suds suppresors, solvents and aesthetic agents.
• the detergent composition herein can be formulated as a variety of compositions, for instance as laundry detergents as well as hard surface cleaners or dishwashing compositions.
• compositions according to the present invention are further illustrated by the following examples.
• EXAMPLE I The following compositions are made by combining the listed ingredients in the listed proportions.
• Peptide aldehyde 1 CH3 ⁇ -(O)C-Phe-Gly-Ala-LeuH
• Peptide aldehyde 2 CH3N-(O)C-Phe-Gly-Ala-LeuH
• Peptide aldehyde 3 CH 3 O-(O)C-Phe-Gly-Ala-PheH
• Peptide aldehyde 4 CH3N-(O)C-Phe-Gly-Ala-PheH
• Peptide aldehyde 5 CH3SO2Phe-Gly-Ala-Leu-H
• Peptide aldehyde 6 CH3SO2Val-Ala-Leu-H
• Peptide aldehyde 7 C 6 H 5 CH 2 O(OH)(O)P-Val-Ala-Leu-H
• Peptide aldehyde 8 CH3CH2SO 2 -Phe-Gly-Ala-Leu-H
• Peptide aldehyde 9 C6H 5 CH 2 SO2-Val-Ala-Leu-H
• Peptide aldehyde 10 C6H5CH O(OH)(O)P-Leu-Ala-Leu-H
• Peptide aldehyde 11 C6H5CH2 ⁇ (OH)(O)P-Phe-Ala-Leu-H
• Peptide aldehyde 12 CH3 ⁇ (OH)(O)P-Leu-Gly-Ala-Leu-H.
• compositions A B C D E F Compositions A B C D E F
• Amylase (143 KNU/g) ⁇ — 0.1 ⁇ — 0.2
• Lipolase® (100KLU/g 0.5 0.2 0.5 0.5 0.4 — commercial solution)
• EXAMPLE II The following formula is tested for % of protease activity remaining. Combinations of 0%, 0.1%, 0.2%, and 0.3% C3++ (from CaCl2) and 0%, 0.0006%, 0.00125%, and 0.0025% peptide aldehyde (Synthesis Example 6) are used. Products are held at 90°F and assayed at weekly intervals for 42 days.

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• 1997
  • 1997-09-19 JP JP10515729A patent/JP2000506930A/ja not_active Withdrawn
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  • 1997-09-19 WO PCT/US1997/016622 patent/WO1998013459A1/en active IP Right Grant
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