AU2012325190B2 - Cleansing composition - Google Patents
Cleansing composition Download PDFInfo
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- AU2012325190B2 AU2012325190B2 AU2012325190A AU2012325190A AU2012325190B2 AU 2012325190 B2 AU2012325190 B2 AU 2012325190B2 AU 2012325190 A AU2012325190 A AU 2012325190A AU 2012325190 A AU2012325190 A AU 2012325190A AU 2012325190 B2 AU2012325190 B2 AU 2012325190B2
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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
-
- 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
-
- 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
-
- 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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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- 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
- 1 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 from 40 to 90% wt pyruvic io acid; 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. is Preferably, the antibacterial component comprises from 0.001 to 5% wt. of the composition. Preferably, the composition comprises a cleansing surfactant. 20 Preferably, the composition is a hard surface cleaning composition. Preferably, the composition is a toilet block composition. Preferably, the composition is a toilet cleaning composition. 25 Preferably, the composition is a handdishwash composition. Preferably, the cleaning composition used according to the invention comprises additionally a detergent surfactant at a concentration between 0 and 50% by 30 weight. Said surfactant (detergent active) is generally chosen from anionic and 5745161_1 (GHMatters) P96467.AU JENNYP 22. Nov. 20'3 15:51 UNILEVER Nr. '343 P. 3 PCT/EP 2012/067 839 - 22-11-2013 G 3183 (V) CPL WO 20131056901 PCT/EP2012/067839 -2 nonionic detergent actives. The cleaning- composition may further comprise cationic, amphoteric and zwitterionic surfactants. Preferably, the total amount of surfactant in said cleaning composition is at least 5 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. Suitable synthetic (non-scap) anionic surfactants are water-soluble salts of organic sulphuric acid mono-esters and sulphonic acids which have in the 10 molecular structure a branched or straight chain alkyl group containing from 6 to 22 carbon atoms in the alkyl part. Examples of such anionic surfactants are water soluble salts of: (primary) long chain (e.g. 6-22 C-atoms) alcohol sulphates (hereinafter 15 referred to as PAS), especially those obtained by sulphating the fatty alcohols produced by reducing the glycerides of tallow or coconut oil; * alkyl benzene sulphonates, such as those in which the alkyl group contains from 6 to 20 carbon atoms; * secondary alkanesulphunates, 20 and mixtures thereof. Also. suitable are the salts of: alkylglyceryl ether sulphates, especially of the ethers of fatty alcohols derived from tallow and coconut oil; 25 + fatty acid monoglyceride sulphates; * sulphates of ethoxylated aliphatic alcohols containing 1-12 ethyleneoxy groups; * 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 30 atoms; .11.2013 15:38:32 - 22.11.2013 15:42:16. This page 3 of 17 AMENDED SHEET1315:39:12 ed at the EPO on Nov 22, 2013 15:42:16. Page 3 of 17 22.lRov. 2013 15:51 UNR EVER Nr.1343 F. 4 PCT/EP 2012/067 839 - 22-11-2013 G 3183 (V) CPL WO 20131056901 PCTIEP2012/067839 -3 * the reaction product of fatty acids esterified with isethionic acid and neutralised with alkali, and mixtures thereof 5 The preferred water-soluble synthetic anionic surfactants are the alkali metal (such as sodium and potassium) and alkaline earth metal (such as calcium and magnesium) salts of alkyl-benzenesulphonates and mixtures with olefinsulphonates and alkyl sulphates, and the fatty acid mono-glyceride sulphates. 10 The most preferred anionic surfactants are alkyl-aromatic sulphonates such as 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, 15 alkylnaphthalene-sulphonates, ammonium diamy[naphthalene-sulphonate, and sodium dinonyl-naphthalene-sulphonate. 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 20 at least 0.5%, more preferably at least 1.0%, but not more than 20%, preferably at most 15%, more preferably at most 10%. A suitable class of nonionic surfactants can be broadly described as compounds produced by the condensation of simple alkylene oxides, which are hydrophilic in 25 nature, with an aliphatic or alkyl-aromatic hydrophobic compound having a reactive hydrogen atom. The length of the hydrophilic or polyoxyalkylene chain 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 30 right HLB, Particular examples include: .11.2013 15:38:32 - 22.11.2013 15:42:16. This page 4of 17 AMENDED SHEET1315:39:28 ed at the EPO on Nov 22, 2013 15:42:16. Page 4 of 17 22. Nov. 2013 15:52 UNR EVER N. 1343 P. 5 PCT/EP 2012/067 839 - 22-11-2013 G 3183 (V) CPL WO 2013/056901 PCT/EP2012/067839 -4 + the condensation products of aliphatic alcohols having from 8 to 22 carbon 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; 5 + condensates of alkylphenols having C6-C15 alkyl groups with 5 to 25 moles of ethylene oxide per mole of alkylphenol; 4 condensate 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 10 to 11,000. Other classes of nonionic surfactants are: - tertiary amine oxides of structure R 1
R
2
R
3 N-, 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 15 of 1 to 3 carbon atoms, e.g. dimethyldodecylamine oxide; * tertiary phosphine oxides of structure R 1
R
2
R
3 P-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 I to 3 carbon atoms, for instance dimethyl-dodecylphosphine oxide; 20 + dialkyl sulphoxides of structure R 1
R
2 =O, where R 1 is an alkyl group of 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; - alkylene oxide condensates of fatty acid alkylolamides; 25 alkyl mercaptans. 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 30 most 20%, preferably not more than 15% and most preferably not more than 10%. .11.2013 15:38:32 - 22.11.2013 15:42:16. This page 5of 17 AMENDED SHEET1315:39:44 ed at the EPO on Nov 22, 2013 15:42:16. Page 5 of 17 22, Nov, 2013 15:52 UNILEVER N u.13L3 P. 6 PCT/EP 2012/067 839 - 22-11-2013 G 3183 (V) CPL Wa 2013/056901 PCT/EP2012/067839 -5 It is also possible optionally to include amphoteric, cationic or zwitterionc surfactants in said compositions. 5 Suitable amphoteric surfactants are derivatives of aliphatic secondary and tertiary amines containing an alkyl group of 8 to 20 carbon atoms and an aliphatic group 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. 10 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. 15 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. 20 Lxamples 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 25 betaine derivatives such as alkyl betaine, in particular C 12
-C
1 6 alkyl betaine, 3 (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 30 wherein the alkylamido group is derived from coconut oil fatty acids. .11.2013 15:38:32 - 22.11.2013 15:42:16. This page 6 of 17 AMENDED SHEET1315:40:00 ed at the EPO on Nov 22, 2013 15:42:16. Page 6 of 17 22.lRov. 2(13 15:52 UNILEVER Kr.1343 P. 7 PCT/EP 2012/067 839 - 22-11-2013 G 3183 (V) CPL WO 2013/056901 PCT/EP2012/067839 -6 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 5 Schwartz, Perry & Berch, Interscience 1958; the current edition of 'McCutcheon's 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 10 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. 15 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 20 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 25 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 30 other ingredients which aid in their cleaning performance. For example, they may .11.2013 15:38:32 - 22.11.2013 15:42:16. This page 7 of 17 AMENDED SHEET 13 15:40:17 ed at the EPO on Nov 22, 2013 15:42:16. Page 7 of 17 22. Nov. 2013 15:52 - UNLR EVER Nr. 1343 P. 8 PCT/EP 2012/067 839 - 22-11-2013 G 3183 (V) CPL WO 2013/056901 PCT/EP2012/067839 -7 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. If present, the builder preferably will form at least 0.1% of the cleaning 5 composition. Suitable inorganic and organic builders are well known to those skilled in the art, 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 10 tendency to produce excessive suds in use. Examples thereof are fatty acids or their salts (soap), isoparaffins, silicone oils and combinations thereof. 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 15 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 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. 20 Where a hydrocarbon solvent is present at a sufficiently high level this may itself provide some or all of the required antifoaming activity. Compositions may also contain, in addition to the ingredients already mentioned, 25 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 compounds), solvents, co-solvents, gel-control agents, further freeze-thaw stabilisers, bactericides, preservatives (for example 1,2-benzisothiazolin-3-one), 30 hydrotropes and perfumes. .11.2013 15:38:32 - 22.11.2013 15:42:16. This page 8of 17 AMENDED SHEET1315:40:33 ed at the EPO on Nov 22, 2013 15:42:16. Page 8 of 17 22. Nov. 2013 15:53 UNR EVER RNr. 1343 P. 9 PCT/EP 2012/067 839 - 22-11-2013 G 3183 (V) CPL WO 2013/056901 PCT/EP20121067839 -8 In a preferred embodiment the composition of the present invention does not comprise tannic acid or related compounds such as gallic acid and/or propyl gallate. It was found that when tannic acid is formulated into alkaline liquid 6 cleaning compositions it produces aesthetically less-pleasing yellow-brown coloured solutions, and it may lead to browning of cement in joints between tiles. In another preferred embodiment the composition of the present invention does not comprise malonic acid. An antioxidant like malonic acid needs relatively high 10 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. In yet another preferred embodiment the composition of the present invention 15 does not comprise formic acid. Formic acid has a pungent odour, and residues on hard surfaces are aesthetically undesirable The composition of the invention may be stored in and dispensed by any suitable means, but spray applicators are particularly preferred. Pump dispensers (whether 20 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 composition is comprised in a container, and wherein the container further comprises a spray dispenser for dispensing said composition in the form of a 25 spray. The spray dispenser is preferably a trigger spray but may be any mechanical means for ejecting the liquid in spray or aerosol form. EXAMPLE 1 30 .11.2013 15:38:32 - 22.11.2013 15:42:16. This page 9 of 17 AMENDED SHEET1315:40:49 ed at the EPO on Nov 22, 2013 15:42:16. Page 9 of 17 22. Nov. 2013 '5:53 UNILEVER r, 1343 P. 10 PCT/EP 2012/067 839 - 22-11-2013 G 3183 (V) CPL WO 2013/056001 PCTIEP20121067839 -9 To ascertain antibacterial efficacy each test mixture was tested against two bacteria typically found on domestic hard surfaces. These were Enterococcus hirae and Staphylococcus aureus. The test mixtures were tested to find the point on the concentration range where 5 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, and 0 the highest concentration. 10 Accordingly, the lower the activity, the better the compound mixture. To test for synergy mathematically in a mixture of n compounds, calculate Total Fractional Activity (TFA) as follows. 15 For each compound i in the mixture (i=1,2, ..- n) , calculate Fractional Activity, FA For compound i, this is defined as: FAI= where A is activity of test mixture of interest and 20 A, is activity of compound i on its own Then the Total Fractional Activity (TFA) for the mixture is calculated as: TFA= where w is weight based on the concentration used and w 1 , 91. 25 Thus if: TFA = 1 then the mixture has additive activity TFA > I then the mixture has antagonistic activity .11.2013 15:38:32 - 22.11.2013 15:42:16. This page 10 of AMENDED SHEET:01315:41:01 ed at the EPO on Nov 22, 2013 15:42:16. Page 10 of 17 22. Nov. 2013 15:53 UNILEVER R. 1343 P. 11 PCT/EP 2012/067 839 - 22-11-2013 G 3183 (V) CPL WO 20131056901 PCT/EP2012/067839 -10 TFA < 1 then the mixture has synergistic activity, and a level of TFA < 0.90 is taken to be strong synergy. This is based on Fractional Inhibitory Concentration work used in biocidal work. 5. For references, see: - Berenbaum MC (1978) A Method for testing synergy with any number of agents. J Infectious Diseases 137(2), 122-130 - Botelho MG (2000) Fractional inhibitory concentration index of combinations 10 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 measure of synergy J.Antimicrobial Chemotherapy 11, 427-433 15 EXAMPLE 2 Bathroom Cleaner: + 0.1 to 10% surfactant, chosen from non-ionic, anionic cationic or amphoteric 20 + 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 01 to 5% organic acid 25 + Optional ingredients o Solvents (0.1-5%) o Polymers (0.01-2%) o Hydrotropes o Buffer 30 o Perfume o Dye o Preservative + Usually pH less than 4 (alkaline variants are available on market, with these containing a sequestrant) 35 Specific Examples .11.2013 15:38:32 - 22.11.2013 15:42:16. This page 11 of 1 AMENDED SHEETO13 15:41:13 ed at the EPO on Nov 22, 2013 15:42:16. Page 11 of 17 22. Ncv. 2013 15:53 JKILEVER N r. 1343 P. 12 PCT/EP 2012/067 839 - 22-11-2013 G 3183 (V) CPL WO 20131056901 PCT/LP2012/067839 - 11 3,5% Neodol 91-8 alcohol ethoxylate non-ionic, SEO 4% Citirc acid 1% Dipropylene glycol n-butyl ether 0.2% Xanthan gum polymer 5 + minors (perfume, dye etc) pH 3.8 5% Neodol 91-8 alcohol ethoxylate non-ionic, SEO 4% Citric acid 10 0.5% Poly acrylic acid + minors (perfume, dye etc) pH4 Kitchen Cleaner: Generic 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 20 - 0-5% Chelating agent * Optional ingredients o Solvents (0.1-5%) o Polymers (0.01-2%) o Hydrotropes 25 o Buffer o Perfume o Dye o Preservative + UsuallypH>10 30 Specific Examples 5% Neodol 91-5 alcohol ethoxylate nonionic, 5EO 4% Monoethanolamine 35 1 % Di-propylene glycol n-butyl ether 0.15% Carbopol EDT2623 cross-linked acrylic polymer + minors (perfume, dye etc) pH 11.2 40 3% Neodol 91-5 alcohol ethoxylate non-Ionic, 5EO 2% SLES 1EO lauryl ether sulphate, 1 EO 4% Monoethanol amine 1 % Dipropylene glycol n-butyl ether .11.2013 15:38:32 - 22.11.2013 15:42:16. This page 12 of AMENDED SHEET:01315:41:25 ed at the EPO on Nov 22, 2013 15:42:16. Page 12 of 17 22. Nov. 2013 15:54 UE LEVER Nr. 1343 P. 13 PCT/EP 2012/067 839 - 22-11-2013 G 3183 (V) CPL WO 2013/056901 PCT/EP2012/067839 -12 pH 11 EXAMPLE4 5 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. 10 * 0.1 to 10% surfactant, chosen from non-ionic, anionic, cationic & amphoteric + Mixtures of the above may be used in any ratlo (limited only by phase behaviour) * Cationic surfactants may be specifically included for hygiene benefits * 0-5% Chelating agent 15 + Optional ingredients o Solvents (0.1-5%) o Polymers (0.01-2%) o Hydrotropes o . Buffer 20 o Perfume o Dye o Preservative * Any pH 25 General Purpose Cleaner (GPC - Floor Cleaner): Specific 3% Neodol 91-5 alcohol ethoxylate non-ionic, 5EQ 1.5% Benzalkyammoinium chloride cationic surfactant 1.5% STP Sodium tri-polyphoshate 30 0.3% Na2CO 3 + minors (perfume, dye etc) pH -11 3% SLES I EQ sodium lauryl ether sulphate, 1 EO 35 1% Citric acid + minors (perfume, dye etc) pH 4 EXAMPLE 5 40 A toilet cleaning composition .11.2013 15:38:32 - 22.11.2013 15:42:16. This page 13 of AMENDED SHEET01315:41:36 ed at the EPO on Nov 22, 2013 15:42:16. Page 13 of 17 22. No v. 2013 15:5 UNILEVER N r. 1343 P. 14 PCT/EP 2012/067 839 - 22-11-2013 G 3183 (V) CPL WO 20131056901 PCTIEP2012/067839 -13- Toilet cleaning products tend to be acidic in nature and have high viscosity and shear thinning properties generated by a rod micellar structure. 0.1 to 10% surfactant, chosen from non-ionic, anionic, cationic & amphoteric 5 Mixtures of the above may be used in any ratio (limited only by phase behaviour) + Cationic surfactants may be specifically included for hygiene benefits + 0-5% bleaching agent 0-10% acid 10 + 0-5% Chelating agent + Optional ingredients o Solvents (0.1-5%) o Polymers (0.01-2%) o Hydrotropes 15 c Buffer o Perfume o Dye o Preservative pH generally <4 20 Toielt cleaner specific example 3% ethomeen BTB12 ethoxylated amine surfactant 4% Sulphamic acid 25 0.5% Sodium cumene sulphonate (hydrotrope) 4% Hydrogen peroxide + minors (perfume, dye etc) pH -1 30 EXAMPLE 6 A Hand dishwash composition Hand Dish Wash (HDW): Generic 35 + 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 40 + Optional ingredients o Solvents (0.1-5%) o Polymers (0.01-2%) .11.2013 15:38:32 - 22.11.2013 15:42:16. This page 14 of AMENDED SHEET:01315:41:49 ed at the EPO on Nov 22, 2013 15:42:16. Page 14 of 17 22. Nov. 2013 15:54 UNILEVER Nr. 1343 P. 15 PCT/EP 2012/067 839 - 22-11-2013 G 3183 (V) CPL WO 2013/056901 PCT/EP2012/067839 -14 o Hydrotropes o Buffer o Perfume o Dye 5 o Preservative Any pH, but tend to be - 4 to 10 HDW: Specific 10 20% SLES 1 EO sodium lauryl ether sulphate, 1 EO 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 15 + minors (perfume, dye etc) pH - 7 11 % NaLAS sodium linear alkyl benzene sulphonate 3.5% SLES 1EO sodium lauryl ether sulphate, 1EO 20 1% MgSO 4 + minors (perfume, dye etc) pH ~ 7 .11.2013 15:38:32 - 22.11.2013 15:42:16. This page 15 of AMENDED SHEET01315:41:57 ed at the EPO on Nov 22, 2013 15:42:16. Page 15 of 17 - 14a It is to be understood that, if any prior art publication is referred to herein, such reference does not constitute an admission that the publication forms a part of the common general knowledge in the art, in Australia or any other country. 5 In the claims which follow and in the preceding description of the invention, except where the context requires otherwise due to express language or necessary implication, the word "comprise" or variations such as "comprises" or "comprising" is used in an inclusive sense, i.e. to specify the presence of the stated features but not to preclude the presence or addition of further features in various 10 embodiments of the invention. 5745161_1 (GHMatters) P96467.AU JENNYP
Claims (1)
- 22. Nov. 2Q13 15:54 UNILEVER Nr. 133 F. 16 PCT/EP 2012/067 839 - 22-11-2013 G 3183 (V) CPL WO 2013/056001 PCTIEP2012/067830 -15 CLAIMS 1. An antibacterial cleansing composition comprising an antibacterial component which comprises from 40 to 90% wt pyruvic acid; from 5 to 55% 5 wt gentisic acid and from 5 to 55% wit of salicylic acid 2. Composition according to claim 1 wherein the antibacterial component comprises from 0.001 to 5% wt. of the composition. 10 3. Composition according to any preceding claim comprising a cleansing surfactant. 4. Composition according to any preceding claim which is a hard surface cleaning composition. 15 5. Composition according to any preceding claim which is a toilet cleaning composition. 6. Composition according to any preceding claim which is a handdishwash 20 composition. .11.2013 15:38:32 - 22.11.2013 15:42:16. This page 16 of AMENDED SHEET01315:42:06 ed at the EPO on Nov 22, 2013 15:42:16. Page 16 of 17
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 AU2012325190A1 (en) | 2014-04-24 |
| AU2012325190B2 true AU2012325190B2 (en) | 2014-09-25 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2012325190A Ceased AU2012325190B2 (en) | 2011-10-18 | 2012-09-12 | Cleansing composition |
Country Status (12)
| 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) |
| PH (1) | PH12014500555A1 (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 |
|---|---|---|---|---|
| CA3147865A1 (en) * | 2019-08-02 | 2021-02-11 | Colgate-Palmolive Company | Toothbrush, system, and method for detecting blood in an oral cavity during toothbrushing |
| CN119776078A (en) * | 2019-12-05 | 2025-04-08 | 宝洁公司 | Cleaning composition |
| WO2023034373A1 (en) * | 2021-08-31 | 2023-03-09 | Colgate-Palmolive Company | Home care compositions |
Citations (5)
| 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 |
| US6106851A (en) * | 1997-06-04 | 2000-08-22 | The Procter & Gamble Company | Mild, rinse-off antimicrobial liquid cleansing compositions containing salicyclic acid |
| US20010046979A1 (en) * | 2000-02-28 | 2001-11-29 | Roselle Brian Joseph | Acidic antimicrobial compositions for treating food and food contact surfaces and methods of use thereof |
| US20040058847A1 (en) * | 2002-09-19 | 2004-03-25 | Clariant Gmbh | Liquid washing and cleaning compositions containing consistency-imparting polymers |
| US20060040837A1 (en) * | 2004-08-17 | 2006-02-23 | Seren Frantz | Low pH structured surfactant compositions |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1276372B1 (en) * | 2000-04-28 | 2005-10-19 | Ecolab Inc. | Antimicrobial composition |
-
2012
- 2012-09-12 PH PH1/2014/500555A patent/PH12014500555A1/en unknown
- 2012-09-12 CN CN201280050910.XA patent/CN103874757A/en active Pending
- 2012-09-12 AU AU2012325190A patent/AU2012325190B2/en not_active Ceased
- 2012-09-12 CA CA2851198A patent/CA2851198A1/en not_active Abandoned
- 2012-09-12 WO PCT/EP2012/067839 patent/WO2013056901A1/en not_active Ceased
- 2012-09-12 MY MYPI2014700936A patent/MY185985A/en unknown
- 2012-09-12 EP EP12756522.4A patent/EP2771448B1/en not_active Not-in-force
- 2012-09-12 EA EA201400480A patent/EA023774B1/en not_active IP Right Cessation
- 2012-09-12 PL PL12756522T patent/PL2771448T3/en unknown
- 2012-09-12 BR BR112014007238A patent/BR112014007238A2/en not_active IP Right Cessation
-
2014
- 2014-03-13 ZA ZA2014/01847A patent/ZA201401847B/en unknown
- 2014-04-11 CL CL2014000924A patent/CL2014000924A1/en unknown
Patent Citations (5)
| 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 |
| US6106851A (en) * | 1997-06-04 | 2000-08-22 | The Procter & Gamble Company | Mild, rinse-off antimicrobial liquid cleansing compositions containing salicyclic acid |
| US20010046979A1 (en) * | 2000-02-28 | 2001-11-29 | Roselle Brian Joseph | Acidic antimicrobial compositions for treating food and food contact surfaces and methods of use thereof |
| US20040058847A1 (en) * | 2002-09-19 | 2004-03-25 | Clariant Gmbh | Liquid washing and cleaning compositions containing consistency-imparting polymers |
| US20060040837A1 (en) * | 2004-08-17 | 2006-02-23 | Seren Frantz | Low pH structured surfactant compositions |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2771448B1 (en) | 2015-12-30 |
| BR112014007238A2 (en) | 2017-04-11 |
| CA2851198A1 (en) | 2013-04-25 |
| PL2771448T3 (en) | 2016-06-30 |
| WO2013056901A1 (en) | 2013-04-25 |
| ZA201401847B (en) | 2016-01-27 |
| AU2012325190A1 (en) | 2014-04-24 |
| EA023774B1 (en) | 2016-07-29 |
| CN103874757A (en) | 2014-06-18 |
| PH12014500555A1 (en) | 2016-12-02 |
| EA201400480A1 (en) | 2016-01-29 |
| EP2771448A1 (en) | 2014-09-03 |
| CL2014000924A1 (en) | 2014-11-21 |
| MY185985A (en) | 2021-06-14 |
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| FGA | Letters patent sealed or granted (standard patent) | ||
| MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |