EP1963474B1 - Réduction des odeurs causées par des produits contenant de l'hypochlorite - Google Patents
Réduction des odeurs causées par des produits contenant de l'hypochlorite Download PDFInfo
- Publication number
- EP1963474B1 EP1963474B1 EP06829482.6A EP06829482A EP1963474B1 EP 1963474 B1 EP1963474 B1 EP 1963474B1 EP 06829482 A EP06829482 A EP 06829482A EP 1963474 B1 EP1963474 B1 EP 1963474B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- diphenylmethane
- alkali metal
- diphenyl oxide
- use according
- weight ratio
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Not-in-force
Links
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 title claims description 20
- 239000000203 mixture Substances 0.000 claims description 25
- 239000003795 chemical substances by application Substances 0.000 claims description 24
- -1 2-methyl naphthyl Chemical group 0.000 claims description 23
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims description 22
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 claims description 21
- 239000003205 fragrance Substances 0.000 claims description 20
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 12
- 239000007844 bleaching agent Substances 0.000 claims description 12
- 239000000460 chlorine Substances 0.000 claims description 12
- 229910052801 chlorine Inorganic materials 0.000 claims description 12
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 claims description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 11
- 229910052783 alkali metal Inorganic materials 0.000 claims description 9
- 150000001412 amines Chemical class 0.000 claims description 7
- 229960003237 betaine Drugs 0.000 claims description 6
- 239000004094 surface-active agent Substances 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- 239000004753 textile Substances 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 3
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 3
- 239000005708 Sodium hypochlorite Substances 0.000 claims description 3
- 229920002125 Sokalan® Polymers 0.000 claims description 3
- 150000007513 acids Chemical class 0.000 claims description 3
- 229910000288 alkali metal carbonate Inorganic materials 0.000 claims description 3
- 150000008041 alkali metal carbonates Chemical class 0.000 claims description 3
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 3
- 229910052910 alkali metal silicate Inorganic materials 0.000 claims description 3
- 125000001476 phosphono group Chemical group [H]OP(*)(=O)O[H] 0.000 claims description 3
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 claims description 3
- 238000004061 bleaching Methods 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims 2
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims 2
- 239000004584 polyacrylic acid Substances 0.000 claims 2
- 235000019645 odor Nutrition 0.000 description 8
- 125000000217 alkyl group Chemical group 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- ZHEGIVZMQJMLMR-UHFFFAOYSA-N 2-methyl-1-(2-methylnaphthalen-1-yl)oxynaphthalene Chemical compound C1=CC=C2C(OC3=C4C=CC=CC4=CC=C3C)=C(C)C=CC2=C1 ZHEGIVZMQJMLMR-UHFFFAOYSA-N 0.000 description 4
- 239000002304 perfume Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 150000003009 phosphonic acids Chemical class 0.000 description 3
- NQMUGNMMFTYOHK-UHFFFAOYSA-N 1-Methoxynaphthalene Natural products C1=CC=C2C(OC)=CC=CC2=C1 NQMUGNMMFTYOHK-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000003352 sequestering agent Substances 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 1
- CIEZZGWIJBXOTE-UHFFFAOYSA-N 2-[bis(carboxymethyl)amino]propanoic acid Chemical compound OC(=O)C(C)N(CC(O)=O)CC(O)=O CIEZZGWIJBXOTE-UHFFFAOYSA-N 0.000 description 1
- 101150065749 Churc1 gene Proteins 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 102100038239 Protein Churchill Human genes 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- YDONNITUKPKTIG-UHFFFAOYSA-N [Nitrilotris(methylene)]trisphosphonic acid Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CP(O)(O)=O YDONNITUKPKTIG-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000002144 chemical decomposition reaction Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229940094506 lauryl betaine Drugs 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- DVEKCXOJTLDBFE-UHFFFAOYSA-N n-dodecyl-n,n-dimethylglycinate Chemical compound CCCCCCCCCCCC[N+](C)(C)CC([O-])=O DVEKCXOJTLDBFE-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229920005646 polycarboxylate Polymers 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 230000019635 sulfation Effects 0.000 description 1
- 238000005670 sulfation reaction Methods 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
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
- C11D3/395—Bleaching agents
- C11D3/3956—Liquid compositions
-
- 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
- C11D3/50—Perfumes
Definitions
- the present invention relates to the use of certain fragrances in hypochlorite-containing bleaches to avoid the unpleasant odor of such agents on human skin, particularly on the hands which has come in contact with the agent.
- Efficient cleaning is one of the requirements that influences the acceptance of such agents by the consumer. This requires providing agents with a wide stain removal potential which can remove, for example, oily and greasy soils from fabrics or hard surfaces such as tiles or tiles.
- hypochlorite bleach containing agents have been developed, among others, in which hypochlorite, as a strong oxidant, contributes to the chemical degradation, destruction and removal of soils.
- Another advantage of using hypochlorite is that it acts as an effective disinfectant.
- a disadvantage is felt that after contact with human skin, which inevitably results in the use of such agents with bare hands and otherwise, for example, when using gloves, can not always avoid a sticking to the skin smell, which can not always be removed even after repeated washing with water.
- EP 0 606 707 describes agents which contain a polymer component together with a hypochlorite compound and lead to a reduction of malodors of the actual agent as well as the surfaces cleaned therewith. This could be due to the high viscosity of these agents, so that compounds responsible for the offensive odor may be trapped in vesicles.
- EP 0 812 909 A1 describes the use of polycarboxylate polymer in hypochlorite-containing bleaches to avoid unpleasant odors resulting from the contact of such agents with skin surfaces.
- EP 0 622 451 deals with the task of odor formation during and after applying chlorine-containing agents and suggests to use a perfume.
- Hypochlorite-containing bleaches containing diphenyloxide and other fragrances are made EP 0 867 503 A2 .
- the present invention is the use of fragrances to reduce the odor of chlorine bleach on human skin, which has come into contact with said chlorine bleach, the fragrance is selected from the group comprising mixtures of diphenylmethane with diphenyl oxide and mixtures of diphenylmethane with diphenyl oxide and with 2-methyl-naphthyl ether, wherein the weight ratio of diphenylmethane to diphenyl oxide is from 1: 1 to 1:50.
- the skin is on a human hand.
- the fragrance preferably has a combination of diphenylmethane and diphenyl oxide in a weight ratio of 1:10 to 1: 5. It furthermore preferably has a combination of diphenylmethane and 2-methylnaphthyl ether in a weight ratio of 50: 1 to 1:10, in particular from 5: 1 to 1: 1. It is also preferred if the fragrance has a combination of diphenyl oxide and 2-methyl-naphthyl ether in a weight ratio of from 250: 1 to 1: 1, in particular from 50: 1 to 5: 1.
- Said fragrance as such or in the form of a preparation containing it, may be applied after the use of the chlorine-containing agent on the skin areas which have come into contact with said agent.
- the fragrance is already part of the composition containing the chlorine bleach.
- the composition is preferably an aqueous liquid which is used undiluted or, if appropriate, after mixing with water on a textile or hard surface and which contains from 0.5% by weight to 10% by weight, in particular from 1% by weight to 6% by weight .-%, of alkali metal hypochlorite, especially sodium hypochlorite contains.
- a liquid hydrous bleach containing alkali metal hypochlorite and fragrance said fragrance being selected from the group consisting of mixtures of diphenylmethane with diphenyloxide and mixtures of diphenylmethane with diphenyloxide and with 2-methyl-naphthyl ether, wherein the weight ratio of diphenylmethane to diphenyloxide is from 1: 1 to 1:50, is selected, is a further object of the invention.
- Another object of the invention is a method for bleaching stains on textiles and / or hard surfaces, in which one uses a composition according to the invention.
- An agent of the invention preferably contains from 0.0005% to 0.005% by weight of diphenylmethane, from 0.005% to 0.025% by weight of diphenyloxide, and / or from 0.0001% to 0.005% by weight of 2 methyl-naphthyl ether.
- a composition according to the invention which may also be used in the context of the use according to the invention, preferably contains 0.1% by weight to 2% by weight of alkali metal hydroxide and up to 5% by weight of palladium-stable surfactant, in particular betaine and / or alkyl ether sulfate.
- R 1 is an alkyl or alkenyl group having 6 to 22 carbon atoms or a group R 4 is CO-NH- (CH 2 ) n -
- R 2 is hydrogen or an alkyl group having 1 to 4 carbon atoms
- R 3 is hydrogen or an alkyl group with 1 to 4 carbon atoms
- R 4 is an alkyl or alkenyl group having 6 to 22 carbon atoms
- m is a number from 1 to 6 and n is a number from 1 to 3.
- surfactants examples include C 12-18 alkyl dimethyl betaine, commercially available as coconut betaine, and C 10-16 alkyl dimethyl betaine, commercially available as lauryl betaine.
- Another class of particularly preferred surfactants are the alkyl ether sulfates obtainable by reacting alcohols (preferably having 6 to 22 carbon atoms) with alkylene oxides, especially ethylene oxide, followed by sulfation and neutralization, especially a C 12-14 fatty alcohol ether sulfate alkoxylated with 2 equivalents of ethylene oxide , In the ether sulfates, the corresponding cation is preferably sodium.
- Surfactants are, if present, preferably in amounts of up to 5 wt .-%, in particular from 0.01 wt .-% to 3 wt .-% in inventive compositions.
- the preparations may additionally comprise sequestering agents, preferably alkylphosphonic acids, and among these in particular those having at least one amine oxide substituent on the alkyl group, referred to herein as amine oxide phosphonic acids, polyacrylic acids and / or polyoxyacids containing phosphono groups, which may also be in the form of their alkali metal salts.
- sequestering agents preferably alkylphosphonic acids, and among these in particular those having at least one amine oxide substituent on the alkyl group, referred to herein as amine oxide phosphonic acids, polyacrylic acids and / or polyoxyacids containing phosphono groups, which may also be in the form of their alkali metal salts.
- amine oxide phosphonic acids are the amine oxide based on aminotrimethylene phosphonic acid. Preferably, from 0.01% to 2% by weight of such sequestering agents are present.
- compositions preferably contain 0.5% by weight to 2% by weight of silicate, in particular alkali metal silicate, and / or 0.1% by weight to 2% by weight of carbonate, in particular alkali metal carbonate.
- compositions according to the invention can be prepared in a simple manner by mixing the abovementioned ingredients in the stated amounts.
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
Claims (20)
- Utilisation de substances odoriférantes pour diminuer l'odeur d'eau de Javel sur la peau humaine qui est entrée en contact avec ladite eau de Javel, caractérisée en ce que la substance odoriférante est choisie parmi le groupe comprenant des mélanges de diphénylméthane avec de l'oxyde de diphényle et des mélanges de diphénylméthane avec de l'oxyde de diphényle et avec de l'éther 2-méthylnaphtylique, le rapport pondéral du diphénylméthane à l'oxyde de diphényle s'élevant de 1:1 à 1:50.
- Utilisation selon la revendication 1, caractérisée en ce que la peau se situe sur une main humaine.
- Utilisation selon la revendication 1 ou 2, caractérisée en ce que la substance odoriférante fait partie de la composition qui contient l'eau de Javel.
- Utilisation selon l'une quelconque des revendications 1 à 3, caractérisée en ce que la substance odoriférante contient du diphénylméthane et de l'oxyde de diphényle dans un rapport pondéral de 1:10 à 1:5.
- Utilisation selon l'une quelconque des revendications 1 à 4, caractérisée en ce que la substance odoriférante contient du diphénylméthane et de l'éther 2-méthylnaphtylique dans un rapport pondéral de 50:1 à 1:10, en particulier de 5:1 à 1:1.
- Utilisation selon l'une quelconque des revendications 1 à 5, caractérisée en ce que la substance odoriférante contient de l'oxyde de diphényle et de l'éther 2-méthylnaphtylique dans un rapport pondéral de 250:1 à 1:1, en particulier de 50:1 à 5:1.
- Utilisation selon l'une quelconque des revendications 3 à 6, caractérisée en ce que la composition est un liquide aqueux que l'on utilise à l'état non dilué ou, de manière facultative, après son mélange avec de l'eau sur une surface textile ou sur une surface dure, et qui contient de 0,5 % en poids à 10 % en poids, en particulier de 1 % en poids à 6 % en poids d'hypochlorite d'un métal alcalin, en particulier d'hypochlorite de sodium.
- Utilisation selon l'une quelconque des revendications 3 à 7, caractérisée en ce que la composition contient de 0,1 % en poids à 2 % en poids d'un hydroxyde de métal alcalin et jusqu'à 5 % en poids d'un agent tensioactif résistant à l'eau de javel, en particulier de bétaïne et/ou d'un alkyléthersulfate.
- Utilisation selon l'une quelconque des revendications 3 à 8, caractérisée en ce que la composition contient de 0,5 % en poids à 2 % en poids d'un silicate, en particulier d'un silicate de métal alcalin, de 0,01 % en poids à 2 % en poids d'un acide organophosphonique et/ou de phosphonate, en particulier d'acide phosphonique d'amine-oxyde, d'acide polyacrylique présentant des groupes phosphono et/ou d'un sel de métal alcalin d'un des acides ou des deux, et/ou de 0,1 % en poids à 2 % en poids d'un carbonate, en particulier d'un carbonate de métal alcalin.
- Utilisation selon l'une quelconque des revendications 3 à 9, caractérisée en ce que la composition contient de 0,0005 % en poids à 0,005 % en poids de diphénylméthane, de 0,005 % en poids à 0,025 % en poids d'oxyde de diphényle et/ou de 0,0001 % en poids à 0,005 % en poids d'éther 2-méthylnaphtylique.
- Utilisation selon l'une quelconque des revendications 3 à 10, caractérisée en ce qu'on mélange la composition, avant son application, avec de l'eau dans des quantités de 1 partie en volume à 100 parties en volume, en particulier de 2 parties en volume à 10 parties en volume pour 1 partie en volume de la composition en particulier liquide.
- Agent de blanchiment aqueux liquide contenant de l'hypochlorite de métal alcalin et une substance odoriférante, caractérisé en ce que la substance odoriférante est choisie parmi le groupe comprenant des mélanges de diphénylméthane avec de l'oxyde de diphényle et des mélanges de diphénylméthane avec de l'oxyde de diphényle et avec de l'éther 2-méthylnaphtylique, le rapport pondéral du diphénylméthane à l'oxyde de diphényle s'élevant de 1:1 à 1:50.
- Agent selon la revendication 12, caractérisé en ce qu'il contient de 0,5 % en poids à 10 % en poids, en particulier de 1 % en poids à 6 % en poids d'hypochlorite d'un métal alcalin, en particulier d'hypochlorite de sodium.
- Agent selon la revendication 12 ou 13, caractérisé en ce qu'il contient de 0,1 % en poids à 2 % en poids d'un hydroxyde de métal alcalin et jusqu'à 5 % en poids d'un agent tensioactif résistant à l'eau de javel, en particulier de bétaïne et/ou d'un alkyléthersulfate.
- Agent selon l'une quelconque des revendications 12 à 14, caractérisé en ce qu'il contient de 0,5 % en poids à 2 % en poids d'un silicate, en particulier d'un silicate de métal alcalin, de 0,01 % en poids à 2 % en poids d'un acide alkylphosphonique et/ou de phosphonate, en particulier d'acide phosphonique d'amine-oxyde, d'acide polyacrylique présentant des groupes phosphono et/ou d'un sel de métal alcalin d'un des acides ou des deux, et/ou de 0,1 % en poids à 2 % en poids d'un carbonate, en particulier d'un carbonate de métal alcalin.
- Agent selon l'une quelconque des revendications 12 à 15, caractérisé en ce qu'il contient du diphénylméthane et de l'oxyde de diphényle dans un rapport pondéral de 1:10 à 1:5.
- Agent selon l'une quelconque des revendications 12 à 16, caractérisé en ce qu'il contient du diphénylméthane et de l'éther 2-méthylnaphtylique dans un rapport pondéral de 50:1 à 1:10, en particulier de 5:1 à 1:1.
- Agent selon l'une quelconque des revendications 12 à 17, caractérisé en ce qu'il contient de l'oxyde de diphényle et de l'éther 2-méthylnaphtylique dans un rapport pondéral de 250:1 à 1:1, en particulier de 50:1 à 5:1.
- Agent selon l'une quelconque des revendications 12 à 18, caractérisé en ce qu'il contient de 0,0005 % en poids à 0,005 % en poids de diphénylméthane, de 0,005 % en poids à 0,025 % en poids d'oxyde de diphényle et/ou de 0,0001 % en poids à 0,005 % en poids d'éther 2-méthylnaphtylique.
- Procédé pour le blanchiment de salissures sur des textiles et/ou sur des surfaces dures, caractérisé en ce qu'on met en oeuvre une composition selon l'une quelconque des revendications 12 à 19.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102005062008A DE102005062008B3 (de) | 2005-12-22 | 2005-12-22 | Geruchsreduktion hypochlorithaltiger Mittel |
| PCT/EP2006/011890 WO2007079870A1 (fr) | 2005-12-22 | 2006-12-11 | Réduction des odeurs causées par des produits contenant de l'hypochlorite |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP1963474A1 EP1963474A1 (fr) | 2008-09-03 |
| EP1963474B1 true EP1963474B1 (fr) | 2016-11-02 |
Family
ID=37811662
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP06829482.6A Not-in-force EP1963474B1 (fr) | 2005-12-22 | 2006-12-11 | Réduction des odeurs causées par des produits contenant de l'hypochlorite |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US8008238B2 (fr) |
| EP (1) | EP1963474B1 (fr) |
| DE (1) | DE102005062008B3 (fr) |
| ES (1) | ES2605747T3 (fr) |
| WO (1) | WO2007079870A1 (fr) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102007034539A1 (de) * | 2007-07-20 | 2009-01-22 | Henkel Ag & Co. Kgaa | Schonendes Bleichmittel |
| US20130216631A1 (en) | 2012-02-17 | 2013-08-22 | The Clorox Company | Targeted performance of hypohalite compositions thereof |
| JP6781866B2 (ja) * | 2018-01-12 | 2020-11-11 | 加地貿易 株式会社 | 塩素系洗浄剤の残り香における塩素臭の消臭剤及び清掃方法 |
Family Cites Families (64)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3393153A (en) * | 1965-12-20 | 1968-07-16 | Procter & Gamble | Novel liquid bleaching compositions |
| US3655566A (en) * | 1970-03-05 | 1972-04-11 | Purex Corp Ltd | Bleach having stable brighteners |
| US3666680A (en) * | 1970-03-05 | 1972-05-30 | Purex Corp Ltd | Method of combining optical brighteners with polymers for stability in bleach and encapsulated product |
| US4193888A (en) * | 1971-09-01 | 1980-03-18 | Colgate-Palmolive Company | Color-yielding scouring cleanser compositions |
| US3876551A (en) * | 1972-02-14 | 1975-04-08 | Int Flavors & Fragrances Inc | Perfumed aqueous hypochlorite composition and method for preparation of same |
| JPS5269415A (en) * | 1975-12-05 | 1977-06-09 | Lion Corp | Liquid deterging and bleaching agents |
| US4116849A (en) | 1977-03-14 | 1978-09-26 | The Procter & Gamble Company | Thickened bleach compositions for treating hard-to-remove soils |
| US4113645A (en) * | 1977-07-26 | 1978-09-12 | Polak's Frutal Works, Inc. | Bleach compositions containing perfume oils |
| JPS57119981A (en) * | 1981-01-19 | 1982-07-26 | Nitto Chem Ind Co Ltd | Method for stabilizing aqueous solution containing chlorine-containing oxidizing agent |
| US4474677A (en) | 1981-11-06 | 1984-10-02 | Lever Brothers Company | Colored aqueous alkalimetal hypochlorite compositions |
| US5180514A (en) * | 1985-06-17 | 1993-01-19 | The Clorox Company | Stabilizing system for liquid hydrogen peroxide compositions |
| US4828723A (en) * | 1987-07-15 | 1989-05-09 | Colgate-Palmolive Company | Stable non-aqueous suspension containing organophilic clay and low density filler |
| US4830782A (en) * | 1987-08-31 | 1989-05-16 | Colgate-Palmolive Company | Hot water wash cycle built nonaqueous liquid nonionic laundry detergent composition containing amphoteric surfactant and method of use |
| GB8723675D0 (en) | 1987-10-08 | 1987-11-11 | Unilever Plc | Sanitizer |
| US5139695A (en) * | 1988-01-14 | 1992-08-18 | Ciba-Geigy Corporation | Stable bleaching compositions containing fluorescent whitening agents |
| US4946619A (en) | 1988-07-19 | 1990-08-07 | The Clorox Company | Solubilization of brighter in liquid hypochlorite |
| US5185096A (en) * | 1991-03-20 | 1993-02-09 | Colgate-Palmolive Co. | Aqueous liquid automatic dishwashing detergent composition comprising hypochlorite bleach and bleach stabilizer |
| EP0439878A1 (fr) | 1990-01-30 | 1991-08-07 | Union Camp Corporation | Détergent sous forme de gel clair pour machines à laver la vaisselle |
| US5057236A (en) | 1990-06-20 | 1991-10-15 | The Clorox Company | Surfactant ion pair fluorescent whitener compositions |
| DE4140830A1 (de) | 1990-12-14 | 1992-06-17 | Ciba Geigy Ag | Einschlussverbindungen |
| US5229027A (en) * | 1991-03-20 | 1993-07-20 | Colgate-Palmolive Company | Aqueous liquid automatic dishwashing detergent composition comprising hypochlorite bleach and an iodate or iodide hypochlorite bleach stabilizer |
| US5232613A (en) | 1991-08-28 | 1993-08-03 | The Procter & Gamble Company | Process for preparing protected particles of water sensitive material |
| EP0565788A1 (fr) | 1992-04-15 | 1993-10-20 | Colgate-Palmolive Company | Composition détergente aqueuse liquide pour le lavage automatique de la vaisselle contenant un agent de blanchiment à base d'hypochlorite et un stabilisateur de blanchiment |
| JP2588345B2 (ja) | 1992-09-16 | 1997-03-05 | 花王株式会社 | 着色液体洗浄漂白剤組成物 |
| US5380458A (en) | 1992-10-02 | 1995-01-10 | Colgate-Palmolive Co. | Stabilized hypohalite compositions |
| WO1994010280A1 (fr) | 1992-11-05 | 1994-05-11 | Wacker-Chemie Gmbh | Nettoyants contenant des cyclodextrines |
| CA2107938C (fr) * | 1993-01-11 | 2005-01-11 | Clement K. Choy | Solutions d'hypochlorite epaisses degageant une odeur reduite d'agent de blanchiment, et methode de production |
| EP0622451B1 (fr) | 1993-04-26 | 1998-12-02 | The Procter & Gamble Company | Compostions parfumées de blanchiment à l'hypochlorite |
| JP2721804B2 (ja) | 1993-12-28 | 1998-03-04 | クリーンケミカル株式会社 | 医療機器用殺菌洗浄剤 |
| CZ60097A3 (en) * | 1994-08-30 | 1997-07-16 | Procter & Gamble | Chelating agents increasing photobleaching |
| CN1102649C (zh) | 1995-08-10 | 2003-03-05 | 雷基特-科尔曼公司 | 具有触变性质的有色流凝清洁组合物 |
| NL1003225C2 (nl) | 1996-05-29 | 1997-12-03 | Heineken Tech Services | Werkwijze voor het reinigen van apparatuur die toegepast is bij het brouwen van bier. |
| EP0812909A1 (fr) * | 1996-06-10 | 1997-12-17 | The Procter & Gamble Company | Utilisation de polymère de polycarboxylate pour réduire l'effet malodorant d'agents de blanchiment sur la peau |
| DE19700799C2 (de) | 1997-01-13 | 1999-02-04 | Henkel Kgaa | Wäßrige Textilbleichmittel |
| AR016292A1 (es) * | 1997-06-27 | 2001-07-04 | Procter & Gamble | Compuesto pro-fragancia, composicion detergente para lavar la ropa, composiciones suavizantes de tejidos y composicion que comprende un sustrato que lo contienen |
| US6083892A (en) * | 1997-08-19 | 2000-07-04 | The Procter & Gamble Company | Automatic dishwashing detergents comprising β-ketoester pro-fragrances |
| DE69737652D1 (de) | 1997-09-19 | 2007-06-06 | Procter & Gamble | Selbstverdickende Bleichmittelzusammensetzungen |
| EP0903403B1 (fr) | 1997-09-19 | 2003-04-16 | The Procter & Gamble Company | Compositions de blanchiment stables |
| EP0905224A1 (fr) | 1997-09-19 | 1999-03-31 | The Procter & Gamble Company | Compositions de blanchiment |
| ATE344832T1 (de) | 1997-09-19 | 2006-11-15 | Procter & Gamble | Verfahren zum bleichen von gewebe |
| US6448214B1 (en) * | 1997-10-08 | 2002-09-10 | The Proctor & Gamble Company | Liquid aqueous bleaching compositions |
| DE19746781A1 (de) * | 1997-10-23 | 1999-04-29 | Henkel Kgaa | Verfahren zur Herstellung duftverstärkter Wasch- oder Reinigungsmittel |
| US5997764A (en) | 1997-12-04 | 1999-12-07 | The B.F. Goodrich Company | Thickened bleach compositions |
| ES2232928T3 (es) | 1998-01-16 | 2005-06-01 | THE PROCTER & GAMBLE COMPANY | Composiciones blanqueantes espesadas, coloreadas, estables. |
| US6448215B1 (en) * | 1998-01-16 | 2002-09-10 | The Procter & Gamble Company | Stable colored thickened bleaching compositions |
| DE19803054A1 (de) | 1998-01-28 | 1999-07-29 | Henkel Kgaa | Bleich- und Desinfektionsmittel |
| US6718992B1 (en) * | 1998-08-27 | 2004-04-13 | Sergio Cardola | Liquid neutral to alkaline hard-surface cleaning composition |
| US6506718B1 (en) * | 1998-09-01 | 2003-01-14 | The Procter & Gamble Company | Bleaching compositions |
| US6894015B1 (en) * | 1998-11-11 | 2005-05-17 | Procter & Gamble Company | Bleaching compositions |
| DE69814398D1 (de) | 1998-11-11 | 2003-06-12 | Procter & Gamble | Bleichmittelzusammensetzungen |
| DE19855329A1 (de) * | 1998-12-01 | 2000-06-08 | Henkel Kgaa | Aktivchlorhaltige Zubereitungen mit stabilisierten optischen Aufhellern |
| DE10015991A1 (de) * | 2000-03-31 | 2001-10-11 | Henkel Kgaa | Textilpflegemittel |
| US20020169091A1 (en) * | 2001-02-14 | 2002-11-14 | Clare Jonathan Richard | Automatic dishwashing compositions comprising blooming perfume and base masking ingredients |
| GB2398571A (en) * | 2003-02-22 | 2004-08-25 | Reckitt Benckiser Inc | Acidic hard surface cleaning and/or disinfecting composition |
| KR100490564B1 (ko) * | 2002-07-23 | 2005-05-19 | 주식회사 메디슨 | 초음파 영상 신호로부터 장기를 인식하는 장치 및 방법 |
| ITMI20021693A1 (it) * | 2002-07-30 | 2004-01-30 | 3V Sigma Spa | Composizioni liquide stabilizzate contenenti cloro attivo |
| EP1462512B1 (fr) | 2003-03-24 | 2007-08-01 | The Procter & Gamble Company | Compositions comprenant complexes de cyclodextrine et au moins un additif pour traitement de lavage |
| US7125833B2 (en) | 2003-03-24 | 2006-10-24 | Wacker Chemie Ag | Cyclodextrin laundry detergent additive complexes and compositions containing same |
| ES2321497T3 (es) | 2003-03-28 | 2009-06-08 | THE PROCTER & GAMBLE COMPANY | Composicion de blanqueo que comprende acido trimetoxibenzoico o una sal del mismo. |
| US6824705B1 (en) * | 2003-05-19 | 2004-11-30 | Colgate-Palmolive Co. | Bleach odor reducing composition |
| US20050101505A1 (en) * | 2003-11-06 | 2005-05-12 | Daniel Wood | Liquid laundry detergent composition having improved color-care properties |
| DE102004020017A1 (de) | 2004-04-21 | 2005-11-17 | Henkel Kgaa | Stark saurer Sanitärreiniger mit stabilisiertem Viskositäts-und Phasenverhalten |
| EP1614742B1 (fr) | 2004-07-08 | 2007-12-05 | The Procter & Gamble Company | Composition de blanchissement comprenant une amine cyclique à empèchement stérique |
| WO2006048104A1 (fr) * | 2004-11-01 | 2006-05-11 | Unilever N.V. | Composition contenant un repulsif a insectes |
-
2005
- 2005-12-22 DE DE102005062008A patent/DE102005062008B3/de not_active Expired - Fee Related
-
2006
- 2006-12-11 WO PCT/EP2006/011890 patent/WO2007079870A1/fr not_active Ceased
- 2006-12-11 EP EP06829482.6A patent/EP1963474B1/fr not_active Not-in-force
- 2006-12-11 ES ES06829482.6T patent/ES2605747T3/es active Active
-
2008
- 2008-06-04 US US12/133,035 patent/US8008238B2/en not_active Expired - Fee Related
Non-Patent Citations (1)
| Title |
|---|
| None * |
Also Published As
| Publication number | Publication date |
|---|---|
| ES2605747T3 (es) | 2017-03-16 |
| US20080261839A1 (en) | 2008-10-23 |
| US8008238B2 (en) | 2011-08-30 |
| DE102005062008B3 (de) | 2007-08-30 |
| WO2007079870A1 (fr) | 2007-07-19 |
| EP1963474A1 (fr) | 2008-09-03 |
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