AU2012325190A1 - Cleansing composition - Google Patents
Cleansing composition Download PDFInfo
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- AU2012325190A1 AU2012325190A1 AU2012325190A AU2012325190A AU2012325190A1 AU 2012325190 A1 AU2012325190 A1 AU 2012325190A1 AU 2012325190 A AU2012325190 A AU 2012325190A AU 2012325190 A AU2012325190 A AU 2012325190A AU 2012325190 A1 AU2012325190 A1 AU 2012325190A1
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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
- C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
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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
- C11D3/20—Organic compounds containing oxygen
- C11D3/2075—Carboxylic acids-salts thereof
- C11D3/2079—Monocarboxylic acids-salts thereof
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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
- C11D3/20—Organic compounds containing oxygen
- C11D3/2075—Carboxylic acids-salts thereof
- C11D3/2082—Polycarboxylic acids-salts thereof
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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
- C11D3/20—Organic compounds containing oxygen
- C11D3/2075—Carboxylic acids-salts thereof
- C11D3/2086—Hydroxy carboxylic acids-salts thereof
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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
- C11D3/20—Organic compounds containing oxygen
- C11D3/2075—Carboxylic acids-salts thereof
- C11D3/2089—Ether acids-salts thereof
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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
- C11D3/26—Organic compounds containing nitrogen
- C11D3/30—Amines; Substituted amines ; Quaternized amines
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- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Detergent Compositions (AREA)
- Cosmetics (AREA)
Abstract
An antibacterial cleansing composition comprising an antibacterial component which comprises one selected from each of the following two groups: A: gentisic acid, 2-methoxybenzoic acid, 4-methoxybenzoic acid, vanillic acid, methyl salicylic acid, salicylic acid, 4-hydroxybenzoic acid, 3-hydroxybenzoic acid, 3, 4-dihydroxybenzoic acid, 4-aminobenzoic acid, gallic acid and o-toluic acid, B: pyruvic, acetic, isobutyric, proprionic, alpha-ketoglutaric and levulinic acids, wherein A is present at from 40-90% weight of the antibacterial component and B is present at from 10 to 60% by weight of the antibacterial component.
Description
WO 2013/056901 PCT/EP2012/067839 CLEANSING COMPOSITION The present invention relates to an anti-bacterial cleansing composition. 5 Despite the prior art there remains a need for improved anti-bacterial cleansing compositions. Particularly, compositions which are able to cleanse hard surfaces. Accordingly, the present invention relates to an antibacterial cleansing composition comprising an antibacterial component which comprises one selected 10 from each of the following two groups: A: gentisic acid, 2-methoxybenzoic acid, 4-methoxybenzoic acid, vanillic acid, methyl salicylic acid, salicylic acid, 4-hydroxybenzoic acid, 3-hydroxybenzoic acid, 3, 4-dihydroxybenzoic acid, 4-aminobenzoic acid, gallic acid and o 15 toluic acid, B: pyruvic, acetic, isobutyric, proprionic, alpha-ketoglutaric and levulinic acids, wherein A is present at from 40-90% weight of the antibacterial component and B 20 is present at from 10 to 60% by weight of the antibacterial component. Preferably, the antibacterial component comprises two members from A. Preferably, the member selected from B is pyruvic acid. 25 Preferably, the member selected from A is gentisic acid or salicylic acid. Preferably, the two members selected from A are gentisic acid and salicylic acid.
WO 2013/056901 PCT/EP2012/067839 -2 Preferably, the antibacterial component comprises gentisic acid, pyruvic acid and salicylic acid. Preferably, the antibacterial component comprises from 40 to 90% wt pyruvic acid; 5 from 5 to 55% wt. gentisic acid and from 5 to 55% wt. salicylic acid. Such compositions are shown by the inventors to have high activity against both enterococcus hirae and staphylococcus aureus. Preferably, the antibacterial component comprises from 0.001 to 5% wt. of the 10 composition. Preferably, the composition comprises a cleansing surfactant. Preferably, the composition is a hard surface cleaning composition. 15 Preferably, the composition is a toilet block composition. Preferably, the composition is a toilet cleaning composition 20 Preferably, the cleaning composition used according to the invention comprises additionally a detergent surfactant at a concentration between 0 and 50% by weight. Said surfactant (detergent active) is generally chosen from anionic and nonionic detergent actives. The cleaning composition may further comprise cationic, amphoteric and zwitterionic surfactants. 25 Preferably, the total amount of surfactant in said cleaning composition is at least 0.1%, more preferably at least 0.5%. The maximum amount is usually less than 30%, more preferably not more than 20%, or even at or below 10%, by weight.
WO 2013/056901 PCT/EP2012/067839 -3 Suitable synthetic (non-soap) anionic surfactants are water-soluble salts of organic sulphuric acid mono-esters and sulphonic acids which have in the molecular structure a branched or straight chain alkyl group containing from 6 to 22 carbon atoms in the alkyl part. 5 Examples of such anionic surfactants are water soluble salts of: * (primary) long chain (e.g. 6-22 C-atoms) alcohol sulphates (hereinafter referred to as PAS), especially those obtained by sulphating the fatty alcohols produced by reducing the glycerides of tallow or coconut oil; 10 e alkyl benzene sulphonates, such as those in which the alkyl group contains from 6 to 20 carbon atoms; * secondary alkanesulphonates; and mixtures thereof. 15 Also suitable are the salts of: * alkylglyceryl ether sulphates, especially of the ethers of fatty alcohols derived from tallow and coconut oil; * fatty acid monoglyceride sulphates; * sulphates of ethoxylated aliphatic alcohols containing 1-12 ethyleneoxy 20 groups; e alkylphenol ethylenoxy-ether sulphates with from 1 to 8 ethyleneoxy units per molecule and in which the alkyl groups contain from 4 to 14 carbon atoms; * the reaction product of fatty acids esterified with isethionic acid and 25 neutralised with alkali, and mixtures thereof. The preferred water-soluble synthetic anionic surfactants are the alkali metal (such as sodium and potassium) and alkaline earth metal (such as calcium and 30 magnesium) salts of alkyl-benzenesulphonates and mixtures with WO 2013/056901 PCT/EP2012/067839 -4 olefinsulphonates and alkyl sulphates, and the fatty acid mono-glyceride sulphates. The most preferred anionic surfactants are alkyl-aromatic sulphonates such as 5 alkylbenzenesulphonates containing from 6 to 20 carbon atoms in the alkyl group in a straight or branched chain, particular examples of which are sodium salts of alkylbenzenesulphonates or of alkyl-toluene-, -xylene- or -phenolsulphonates, alkylnaphthalene-sulphonates, ammonium diamylnaphthalene-sulphonate, and sodium dinonyl-naphthalene-sulphonate. 10 If synthetic anionic surfactant is to be employed the amount present in the cleaning compositions of the invention will generally be at least 0.1%, preferably at least 0.5%, more preferably at least 1.0%, but not more than 20%, preferably at most 15%, more preferably at most 10%. 15 A suitable class of nonionic surfactants can be broadly described as compounds produced by the condensation of simple alkylene oxides, which are hydrophilic in nature, with an aliphatic or alkyl-aromatic hydrophobic compound having a reactive hydrogen atom. The length of the hydrophilic or polyoxyalkylene chain 20 which is attached to any particular hydrophobic group can be readily adjusted to yield a compound having the desired balance between hydrophilic and hydrophobic elements. This enables the choice of nonionic surfactants with the right HLB. Particular examples include: * the condensation products of aliphatic alcohols having from 8 to 22 carbon 25 atoms in either straight or branched chain configuration with ethylene oxide, such as a coconut alcohol/ethylene oxide condensates having from 2 to 15 moles of ethylene oxide per mole of coconut alcohol; e condensates of alkylphenols having C6-C1 5 alkyl groups with 5 to 25 moles of ethylene oxide per mole of alkylphenol; WO 2013/056901 PCT/EP2012/067839 -5 * condensates of the reaction product of ethylene-diamine and propylene oxide with ethylene oxide, the condensates containing from 40 to 80% of ethyleneoxy groups by weight and having a molecular weight of from 5,000 to 11,000. 5 Other classes of nonionic surfactants are: * tertiary amine oxides of structure R 1
R
2
R
3 N-O, where R' is an alkyl group of 8 to 20 carbon atoms and R 2 and R 3 are each alkyl or hydroxyalkyl groups of 1 to 3 carbon atoms, e.g. dimethyldodecylamine oxide; 10 e tertiary phosphine oxides of structure R 1
R
2
R
3 P-O, where R 1 is an alkyl group of 8 to 20 carbon atoms and R 2 and R 3 are each alkyl or hydroxyalkyl groups of 1 to 3 carbon atoms, for instance dimethyl-dodecylphosphine oxide; e dialkyl sulphoxides of structure R 1
R
2 S=O, where R 1 is an alkyl group of 15 from 10 to 18 carbon atoms and R 2 is methyl or ethyl, for instance methyl tetradecyl sulphoxide; * fatty acid alkylolamides, such as the ethanol amides; e alkylene oxide condensates of fatty acid alkylolamides; e alkyl mercaptans. 20 The concentration of the nonionic surfactant other than APG to be employed in said cleaning composition of the invention will preferably be at least 0.1%, more preferably at least 0.5%, most preferably at least 1%. The amount is suitably at most 20%, preferably not more than 15% and most preferably not more than 10%. 25 It is also possible optionally to include amphoteric, cationic or zwitterionic surfactants in said compositions. Suitable amphoteric surfactants are derivatives of aliphatic secondary and tertiary 30 amines containing an alkyl group of 8 to 20 carbon atoms and an aliphatic group WO 2013/056901 PCT/EP2012/067839 -6 substituted by an anionic water-solubilising group, for instance sodium 3 dodecylamino-propionate, sodium 3-dodecylaminopropane-sulphonate and sodium N-2-hydroxy-dodecyl-N-methyltaurate. 5 Examples of suitable cationic surfactants can be found among quaternary ammonium salts having one or two alkyl or aralkyl groups of from 8 to 20 carbon atoms and two or three small aliphatic (e.g. methyl) groups, for instance cetyltrimethylammonium chloride. 10 A specific group of surfactants are the tertiary amines obtained by condensation of ethylene and/or propylene oxide with long chain aliphatic amines. The compounds behave like nonionic surfactants in alkaline medium and like cationic surfactants in acid medium. 15 Examples of suitable zwitterionic surfactants can be found among derivatives of aliphatic quaternary ammonium, sulphonium and phosphonium compounds having an aliphatic group of from 8 to 18 carbon atoms and an aliphatic group substituted by an anionic water-solubilising group, for instance betaine and betaine derivatives such as alkyl betaine, in particular C12-C16 alkyl betaine, 3 20 (N,N-dimethyl-N-hexadecylammonium)-propane-1-sulphonate betaine, 3 (dodecylmethyl-sulphonium)-propane-1 -sulphonate betaine, 3-(cetylmethyl phosphonium)-propane-1 -sulphonate betaine and N,N-dimethyl-N-dodecyl glycine. Other well known betaines are the alkylamidopropyl betaines e.g. those wherein the alkylamido group is derived from coconut oil fatty acids. 25 Further examples of suitable surfactants are compounds commonly used as surface-active agents given in the well-known textbooks: 'Surface Active Agents' Vol.1, by Schwartz & Perry, Interscience 1949; 'Surface Active Agents' Vol.2 by Schwartz, Perry & Berch, Interscience 1958; the current edition of 'McCutcheon's WO 2013/056901 PCT/EP2012/067839 -7 Emulsifiers and Detergents' published by Manufacturing Confectioners Company; 'Tenside-Taschenbuch', H. Stache, 2nd Edn., Carl Hauser Verlag, 1981. In a preferred embodiment the composition according to the invention has a pH of 5 from 2 to 13, more preferably at least 3, and not more than 12. Cleaning methods of the invention intended for cleaning kitchen hard surfaces may advantageously be carried out at a pH in the alkaline range. Preferably the method of the invention is carried out either at a pH between roughly 6.0 and 12, more preferred between 7.0 and 10. 10 The pH of the cleaning composition used in the method of the invention may be adjusted with organic or inorganic acids or bases. Preferred inorganic bases are preferably alkali or alkaline earth hydroxides, ammonia, carbonates or bicarbonates, the alkali metal preferably being sodium or potassium or the alkaline 15 earth metal preferably being calcium or magnesium. The organic bases are preferably amines, alkanolamines and other suitable amino compounds. Inorganic acids may include hydrochloric acid, sulphuric acid or phosphoric acid, and organic acids may include acetic acid, citric acid or formic acid as well as dicarboxylic acid mixtures such as Radimix (trade mark, Radici Group) and 20 Sokalan DCS (trade mark, BASF). The cleaning composition used according to the present invention may include abrasives. In a preferred embodiment the composition used according to the present invention does not contain an abrasive. The compositions may contain 25 other ingredients which aid in their cleaning performance. For example, they may contain detergent builders and mixtures of builders in an amount of up to 25%, in particular when the composition contains one or more anionic surfactants.
WO 2013/056901 PCT/EP2012/067839 -8 If present, the builder preferably will form at least 0.1% of the cleaning composition. Suitable inorganic and organic builders are well known to those skilled in the art. 5 A further optional ingredient for compositions used according to the invention is a suds regulating material, which can be employed in compositions which have a tendency to produce excessive suds in use. Examples thereof are fatty acids or their salts (soap), isoparaffins, silicone oils and combinations thereof. 10 Soaps are salts of fatty acids and include alkali metal soaps such as the sodium, potassium and ammonium salts of fatty acids containing from about 8 to about 24 carbon atoms, and preferably from about 10 to about 20 carbon atoms. Particularly useful are the sodium and potassium and mono-, di- and triethanolamine salts of the mixtures of fatty acids derived from palm oil, coconut 15 oil and ground nut oil. When employed, the amount of fatty acid or soap can form at least 0.005%, preferably 0.1% to 2% by weight of the composition. Where a hydrocarbon solvent is present at a sufficiently high level this may itself provide some or all of the required antifoaming activity. 20 Compositions may also contain, in addition to the ingredients already mentioned, various other optional ingredients such as colourants, whiteners, optical brighteners, soil suspending agents, detersive enzymes, compatible bleaching agents (particularly peroxide compounds and active chlorine releasing 25 compounds), solvents, co-solvents, gel-control agents, further freeze-thaw stabilisers, bactericides, preservatives (for example 1,2-benzisothiazolin-3-one), hydrotropes and perfumes. In a preferred embodiment the composition of the present invention does not 30 comprise tannic acid or related compounds such as gallic acid and/or propyl WO 2013/056901 PCT/EP2012/067839 -9 gallate. It was found that when tannic acid is formulated into alkaline liquid cleaning compositions it produces aesthetically less-pleasing yellow-brown coloured solutions, and it may lead to browning of cement in joints between tiles. 5 In another preferred embodiment the composition of the present invention does not comprise malonic acid. An antioxidant like malonic acid needs relatively high concentrations to achieve a next time cleaning benefit. Moreover consumers may regard residues of malonic acid on the hard surfaces in e.g. kitchen and bathroom to be harmful and undesired. 10 In yet another preferred embodiment the composition of the present invention does not comprise formic acid. Formic acid has a pungent odour, and residues on hard surfaces are aesthetically undesirable. 15 The composition of the invention may be stored in and dispensed by any suitable means, but spray applicators are particularly preferred. Pump dispensers (whether spray or non-spray pumps) and pouring applicators (bottles etc) are also possible. Thus, in a preferred embodiment the second aspect of the invention provides the use of an aqueous cleaning composition according to the invention, wherein said 20 composition is comprised in a container, and wherein the container further comprises a spray dispenser for dispensing said composition in the form of a spray. The spray dispenser is preferably a trigger spray but may be any mechanical means for ejecting the liquid in spray or aerosol form. 25 EXAMPLE 1 To ascertain antibacterial efficacy each test mixture was tested against two bacteria typically found on domestic hard surfaces. These were Enterococcus 30 hirae and Staphylococcus aureus.
WO 2013/056901 PCT/EP2012/067839 -10 The test mixtures were tested to find the point on the concentration range where 50% kill is achieved. This point defines the activity measure, A. In this analysis, the activity is scaled so that 1 = the lowest concentration possible, 5 and 0 = the highest concentration. Accordingly, the lower the activity, the better the compound mixture. To test for synergy mathematically in a mixture of n compounds, calculate Total 10 Fractional Activity (TFA) as follows. For each compound i in the mixture (i=1,2,.. n) , calculate Fractional Activity, FA; For compound i, this is defined as: 15 FA;= mix where Amix is activity of test mixture of interest and A; is activity of compound ion its own Then the Total Fractional Activity (TFA) for the mixture is calculated as: 20 TFA = wFA n where w; is weight based on the concentration used and w =1. Thus if: TFA = 1 then the mixture has additive activity TFA > 1 then the mixture has antagonistic activity 25 TFA < 1 then the mixture has synergistic activity, and a level of TFA < 0.90 is taken to be strong synergy.
WO 2013/056901 PCT/EP2012/067839 - 11 This is based on Fractional Inhibitory Concentration work used in biocidal work. For references, see: - Berenbaum MC (1978) A Method for testing synergy with any number of 5 agents. J.Infectious Diseases 137(2), 122-130 - Botelho MG (2000) Fractional inhibitory concentration index of combinations of antibacterial agents against cariogenic organisms. J.Dentistry 28, 565 570. - Hall, M.J. et al (1983) The fractional inhibitory concentration (FIC) index as a 10 measure of synergy J.Antimicrobial Chemotherapy 11, 427-433 EXAMPLE 2 This table shows the antibacterial test results against entercoccus and 15 staphylococcus aureus. Entero Staph Synergy Synergy Source X Y Z measure Summary measure Summary 120 0 0 . . 0 120 0 . . 0 0 120 . . 1 10 110 0 0.51 Synergy 2 10 110 0 1.02 Additive 0.54 Synergy 3 20 100 0 3.99 Antagonistic 4 20 100 0 4.46 Antagonistic 5.63 Antagonistic 5 30 90 0 1.54 Antagonistic 6 30 90 0 4.12 Antagonistic 4.38 Antagonistic 7 30 90 0 2.25 Antagonistic 1.47 Antagonistic 8 40 80 0 1.18 Antagonistic 1.13 Antagonistic 9 40 80 0 0.93 Additive 0.19 Synergy 10 40 80 0 0.89 Synergy 0.65 Synergy 11 40 80 0 4.03 No activity 2.63 No activity 12 40 80 0 3.77 Antagonistic 6.11 Antagonistic 13 50 70 0 5.20 Antagonistic .
WO 2013/056901 PCT/EP2012/067839 -12 14 60 60 0 5.60 Antagonistic 15 60 60 0 1.82 Antagonistic 5.53 Antagonistic 16 60 60 0 0.59 Synergy 0.75 Synergy 17 60 60 0 2.53 Antagonistic 2.24 No activity 18 60 60 0 2.09 Antagonistic 6.58 Antagonistic 19 60 60 0 1.18 Antagonistic 1.22 Antagonistic 20 80 40 0 0.58 Synergy 1.88 Antagonistic 21 80 40 0 3.61 Antagonistic 0.86 Synergy 22 80 40 0 2.55 No activity 1.32 Antagonistic 23 80 40 0 1.73 Antagonistic 7.06 Antagonistic 24 90 30 0 1.30 Antagonistic 5.50 Antagonistic 25 90 30 0 0.78 Synergy 1.77 Antagonistic 26 100 20 0 0.11 Synergy 0.32 Synergy 27 100 20 0 1.36 Antagonistic 7.54 Antagonistic 28 110 10 0 0.60 Synergy 0.26 Synergy 29 20 0 100 3.41 Antagonistic 30 30 0 90 2.45 Antagonistic 8.86 Antagonistic 31 40 0 80 0.43 Synergy 2.87 Antagonistic 32 60 0 60 0.15 Synergy 0.68 Synergy 33 60 0 60 1.97 Antagonistic 8.13 Antagonistic 34 60 0 60 5.85 No activity 2.01 Antagonistic 35 80 0 40 6.32 Antagonistic 0.90 Synergy 36 90 0 30 1.48 Antagonistic 6.77 Antagonistic 37 0 20 100 8.94 Antagonistic 38 0 30 90 2.98 Antagonistic 39 0 30 90 3.49 Antagonistic 6.29 Antagonistic 40 0 40 80 2.57 Antagonistic 41 0 50 70 3.43 Antagonistic 42 0 60 60 3.02 Antagonistic 43 0 60 60 4.32 No activity 6.09 Antagonistic 44 0 90 30 3.13 Antagonistic 4.30 Antagonistic 45 10 60 50 1.50 Antagonistic 0.19 Synergy 46 20 40 60 0.77 Synergy 0.79 Synergy 47 20 70 30 1.86 Antagonistic 4.95 Antagonistic 48 30 30 60 2.35 Antagonistic 6.77 Antagonistic 49 30 60 30 3.56 Antagonistic 5.93 Antagonistic 50 30 60 30 1.80 Antagonistic 51 40 20 60 2.36 Antagonistic 52 50 30 40 0.81 Synergy 0.54 Synergy 53 50 50 20 0.24 Synergy 0.40 Synergy WO 2013/056901 PCT/EP2012/067839 -13 54 50 50 20 1.35 Antagonistic 55 60 30 30 0.47 Synergy 0.49 Synergy 56 60 30 30 2.52 Antagonistic 6.45 Antagonistic 57 60 50 10 0.54 Synergy 0.31 Synergy 58 70 40 10 0.50 Synergy 0.36 Synergy 59 80 20 20 1.27 Antagonistic 0.71 Synergy Test mixtures comprising higher levels of pyruvic acid, gentisic acid and salicylic acid are seen to have high synergistic activity against both test organisms. 5 EXAMPLE 3 Bathroom Cleaner: * 0.1 to 10% surfactant, chosen from non-ionic, anionic cationic or amphoteric 10 e Mixtures of the above may be used in any ratio (limited only by phase behaviour) * Cationic surfactants may be specifically included if a hygiene element is required * 0.1 to 5% organic acid 15 e Optional ingredients o Solvents (0.1-5%) o Polymers (0.01 -2%) o Hydrotropes o Buffer 20 o Perfume o Dye o Preservative * Usually pH less than 4 (alkaline variants are available on market, with these containing a sequestrant) 25 Specific Examples 3.5% Neodol 91-8 alcohol ethoxylate non-ionic, 8EO 4% Citirc acid 30 1 % Dipropylene glycol n-butyl ether 0.2% Xanthan gum polymer + minors (perfume, dye etc) pH 3.8 35 5% Neodol 91-8 alcohol ethoxylate non-ionic, 8EO WO 2013/056901 PCT/EP2012/067839 - 14 4% Citric acid 0.5% Poly acrylic acid + minors (perfume, dye etc) pH 4 5 Kitchen Cleaner: Generic * 0.1 to 10% surfactant, chosen from non-ionic, anionic, cationic & amphoteric * Mixtures of the above may be used in any ratio (limited only by phase 10 behaviour) * Cationic surfactants may be specifically included for hygiene benefits * 0-5% Chelating agent * Optional ingredients o Solvents (0.1-5%) 15 o Polymers (0.01 -2%) o Hydrotropes o Buffer o Perfume o Dye 20 o Preservative * Usually pH >10 Specific Examples 25 5% Neodol 91-5 alcohol ethoxylate nonionic, 5EO 4% Monoethanolamine 1 % Di-propylene glycol n-butyl ether 0.15% Carbopol EDT2623 cross-linked acrylic polymer + minors (perfume, dye etc) 30 pH 11.2 3% Neodol 91-5 alcohol ethoxylate non-ionic, 5EO 2% SLES 1 EO lauryl ether sulphate, 1 EO 4% Monoethanol amine 35 1 % Dipropylene glycol n-butyl ether pH 11 EXAMPLE 4 40 General Purpose Cleaner (GPC - Floor Cleaner): Generic GPC's tend contain a lower level of components at reduced levels in comparison to Kitchen & Bathroom specialist cleaners.
WO 2013/056901 PCT/EP2012/067839 -15 * 0.1 to 10% surfactant, chosen from non-ionic, anionic, cationic & amphoteric * Mixtures of the above may be used in any ratio (limited only by phase behaviour) * Cationic surfactants may be specifically included for hygiene benefits 5 e 0-5% Chelating agent * Optional ingredients o Solvents (0.1-5%) o Polymers (0.01 -2%) o Hydrotropes 10 o Buffer o Perfume o Dye o Preservative * Any pH 15 General Purpose Cleaner (GPC - Floor Cleaner): Specific 3% Neodol 91-5 alcohol ethoxylate non-ionic, 5EO 1.5% Benzalkyammoinium chloride cationic surfactant 20 1.5% STP Sodium tri-polyphoshate 0.3% Na 2 CO3 + minors (perfume, dye etc) pH -11 25 3% SLES 1 EO sodium lauryl ether sulphate, 1 EO 1% Citric acid + minors (perfume, dye etc) pH 4 30 EXAMPLE 5 A toilet cleaning composition Toilet cleaning products tend to be acidic in nature and have high viscosity and 35 shear thinning properties generated by a rod micellar structure. * 0.1 to 10% surfactant, chosen from non-ionic, anionic, cationic & amphoteric * Mixtures of the above may be used in any ratio (limited only by phase behaviour) 40 e Cationic surfactants may be specifically included for hygiene benefits * 0-5% bleaching agent * 0-10% acid * 0-5% Chelating agent WO 2013/056901 PCT/EP2012/067839 -16 e Optional ingredients o Solvents (0.1-5%) o Polymers (0.01 -2%) o Hydrotropes 5 o Buffer o Perfume o Dye o Preservative * pH generally <4 10 Toielt cleaner specific example 3% ethomeen BTB12 ethoxylated amine surfactant 4% Sulphamic acid 15 0.5% Sodium cumene sulphonate (hydrotrope) 4% Hydrogen peroxide + minors (perfume, dye etc) pH -1 20 EXAMPLE 6 A Hand dishwash composition Hand Dish Wash (HDW) : Generic 25 e 0.1 to 40% surfactant, with surfactant chosen from anionic, non-ionic, cationic or amphoteric * Mixtures of the above may be used in any ratio (limited only by phase behaviour) * Cationic surfactants may be specifically included for hygiene benefits 30 e Optional ingredients o Solvents (0.1-5%) o Polymers (0.01 -2%) o Hydrotropes o Buffer 35 o Perfume o Dye o Preservative * Any pH, but tend to be - 4 to 10 40 HDW: Specific 20% SLES 1 EO sodium lauryl ether sulphate, 1 EO WO 2013/056901 PCT/EP2012/067839 -17 8% NaLAS sodium linear alkyl benzene sulphonate 5% CAPB Cocoamido propyl betaine 1 % Neodol 91-8 alcohol ethoxylate non-ionic, 8EO 2.5% MgSO 4 5 + minors (perfume, dye etc) pH - 7 11% NaLAS sodium linear alkyl benzene sulphonate 3.5% SLES 1 EO sodium lauryl ether sulphate, 1 EO 10 1% MgSO 4 + minors (perfume, dye etc) pH - 7
Claims (12)
1. An antibacterial cleansing composition comprising an antibacterial component which comprises one selected from each of the following two 5 groups: A: gentisic acid, 2-methoxybenzoic acid, 4-methoxybenzoic acid, vanillic acid, methyl salicylic acid, salicylic acid, 4-hydroxybenzoic acid, 3 hydroxybenzoic acid, 3, 4-dihydroxybenzoic acid, 4-aminobenzoic acid, 10 gallic acid and o-toluic acid, B: pyruvic, acetic, isobutyric, proprionic, alpha-ketoglutaric and levulinic acids, 15 wherein A is present at from 40-90% weight of the antibacterial component and B is present at from 10 to 60% by weight of the antibacterial component.
2. Composition according to claim 1 wherein the antibacterial component 20 comprises two members from A.
3. Composition according to claim 1 or 2 wherein the member selected from B is pyruvic acid. 25
4. Composition according to any preceding claim wherein the member selected from A is gentisic acid or salicylic acid.
5. Composition according to claim 2 wherein the two members selected from A are gentisic acid and salicylic acid. 30 WO 2013/056901 PCT/EP2012/067839 -19
6. Composition according to any preceding claim wherein the antibacterial component comprises gentisic acid, pyruvic acid and salicylic acid.
7. Composition according to claim 6 wherein the antibacterial component 5 comprises from 40 to 90% wt pyruvic acid; from 5 to 55% wt. gentisic acid and from 5 to 55% wt. salicylic acid.
8. Composition according to any preceding claim wherein the antibacterial component comprises from 0.001 to 5% wt. of the composition. 10
9. Composition according to any preceding claim comprising a cleansing surfactant.
10.Composition according to any preceding claim which is a hard surface 15 cleaning composition.
11. Composition according to any preceding claim which is a toilet cleaning composition. 20
12.Composition according to any preceding claim which is a handdishwash composition.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP11185605.0 | 2011-10-18 | ||
EP11185605 | 2011-10-18 | ||
PCT/EP2012/067839 WO2013056901A1 (en) | 2011-10-18 | 2012-09-12 | Cleansing composition |
Publications (2)
Publication Number | Publication Date |
---|---|
AU2012325190A1 true AU2012325190A1 (en) | 2014-04-24 |
AU2012325190B2 AU2012325190B2 (en) | 2014-09-25 |
Family
ID=46826559
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2012325190A Ceased AU2012325190B2 (en) | 2011-10-18 | 2012-09-12 | Cleansing composition |
Country Status (11)
Country | Link |
---|---|
EP (1) | EP2771448B1 (en) |
CN (1) | CN103874757A (en) |
AU (1) | AU2012325190B2 (en) |
BR (1) | BR112014007238A2 (en) |
CA (1) | CA2851198A1 (en) |
CL (1) | CL2014000924A1 (en) |
EA (1) | EA023774B1 (en) |
MY (1) | MY185985A (en) |
PL (1) | PL2771448T3 (en) |
WO (1) | WO2013056901A1 (en) |
ZA (1) | ZA201401847B (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2019460184B2 (en) * | 2019-08-02 | 2023-05-18 | Colgate-Palmolive Company | Toothbrush, system, and method for detecting blood in an oral cavity during toothbrushing |
EP4069810A1 (en) * | 2019-12-05 | 2022-10-12 | The Procter & Gamble Company | Cleaning composition |
AU2022340559A1 (en) * | 2021-08-31 | 2024-02-29 | Colgate-Palmolive Company | Home care compositions |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3434885A1 (en) * | 1984-09-22 | 1986-03-27 | Werner Prof. Dr. 2000 Hamburg Thorn | Orally administrable composition |
AU7706698A (en) * | 1997-06-04 | 1998-12-21 | Procter & Gamble Company, The | Mild, rinse-off antimicrobial liquid cleansing compositions containing salicylicacid |
BR0108734B1 (en) * | 2000-02-28 | 2013-04-24 | stabilized, concentrated, acidic antimicrobial composition, its production process, as well as method of cleaning and / or reducing microorganisms in foods. | |
DE60114174T2 (en) * | 2000-04-28 | 2006-07-20 | Ecolab Inc., St. Paul | ANTIMICROBIAL COMPOSITION |
DE10243661A1 (en) * | 2002-09-19 | 2004-04-01 | Clariant Gmbh | Liquid washing and cleaning agents with consistency-giving polymers |
US20060040837A1 (en) * | 2004-08-17 | 2006-02-23 | Seren Frantz | Low pH structured surfactant compositions |
-
2012
- 2012-09-12 CN CN201280050910.XA patent/CN103874757A/en active Pending
- 2012-09-12 BR BR112014007238A patent/BR112014007238A2/en not_active IP Right Cessation
- 2012-09-12 EP EP12756522.4A patent/EP2771448B1/en not_active Not-in-force
- 2012-09-12 WO PCT/EP2012/067839 patent/WO2013056901A1/en active Application Filing
- 2012-09-12 EA EA201400480A patent/EA023774B1/en not_active IP Right Cessation
- 2012-09-12 MY MYPI2014700936A patent/MY185985A/en unknown
- 2012-09-12 AU AU2012325190A patent/AU2012325190B2/en not_active Ceased
- 2012-09-12 PL PL12756522T patent/PL2771448T3/en unknown
- 2012-09-12 CA CA2851198A patent/CA2851198A1/en not_active Abandoned
-
2014
- 2014-03-13 ZA ZA2014/01847A patent/ZA201401847B/en unknown
- 2014-04-11 CL CL2014000924A patent/CL2014000924A1/en unknown
Also Published As
Publication number | Publication date |
---|---|
BR112014007238A2 (en) | 2017-04-11 |
CN103874757A (en) | 2014-06-18 |
WO2013056901A1 (en) | 2013-04-25 |
EA023774B1 (en) | 2016-07-29 |
MY185985A (en) | 2021-06-14 |
EP2771448A1 (en) | 2014-09-03 |
EA201400480A1 (en) | 2016-01-29 |
PL2771448T3 (en) | 2016-06-30 |
ZA201401847B (en) | 2016-01-27 |
EP2771448B1 (en) | 2015-12-30 |
CA2851198A1 (en) | 2013-04-25 |
CL2014000924A1 (en) | 2014-11-21 |
AU2012325190B2 (en) | 2014-09-25 |
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