ZA200304587B - Alkaline cleaning and sanitizing composition effective for soap scum removal. - Google Patents

Alkaline cleaning and sanitizing composition effective for soap scum removal. Download PDF

Info

Publication number: ZA200304587B
Authority: ZA; South Africa
Prior art keywords: constituent; composition according; composition; surfactant; agents
Prior art date: 2000-12-15

Application number

ZA200304587A

Other languages

English (en)

Inventor

Colurciello Andrew Francis

Weibel Albert Thomas

Bennett Mark Timothy

Original Assignee

Reckitt Benckiser Inc

Priority date (The priority date 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 date listed.)

2000-12-15

Filing date

2003-06-12

Publication date

2004-06-25

2003-06-12 Application filed by Reckitt Benckiser Inc filed Critical Reckitt Benckiser Inc

2004-06-25 Publication of ZA200304587B publication Critical patent/ZA200304587B/en

Links

239000000203 mixture Substances 0.000 title claims description 87
238000004140 cleaning Methods 0.000 title claims description 20
239000000344 soap Substances 0.000 title claims description 15
238000011012 sanitization Methods 0.000 title claims description 13
239000000470 constituent Substances 0.000 claims description 40
-1 organic acid compound Chemical class 0.000 claims description 29
239000004094 surface-active agent Substances 0.000 claims description 21
239000002738 chelating agent Substances 0.000 claims description 17
230000002070 germicidal effect Effects 0.000 claims description 16
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
150000001412 amines Chemical class 0.000 claims description 11
125000000217 alkyl group Chemical group 0.000 claims description 10
239000003960 organic solvent Substances 0.000 claims description 10
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 9
150000003856 quaternary ammonium compounds Chemical group 0.000 claims description 8
239000000654 additive Substances 0.000 claims description 7
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 6
239000000872 buffer Substances 0.000 claims description 5
239000003086 colorant Substances 0.000 claims description 5
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 5
239000003205 fragrance Substances 0.000 claims description 5
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 5
239000003002 pH adjusting agent Substances 0.000 claims description 5
239000002562 thickening agent Substances 0.000 claims description 5
150000001340 alkali metals Chemical class 0.000 claims description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 4
DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims description 3
229910052783 alkali metal Inorganic materials 0.000 claims description 3
229910000272 alkali metal oxide Inorganic materials 0.000 claims description 2
229910052784 alkaline earth metal Inorganic materials 0.000 claims description 2
229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 claims description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
238000007046 ethoxylation reaction Methods 0.000 claims description 2
238000000034 method Methods 0.000 claims description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
230000000249 desinfective effect Effects 0.000 claims 1
125000005843 halogen group Chemical group 0.000 claims 1
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 13
239000000463 material Substances 0.000 description 8
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
150000001298 alcohols Chemical class 0.000 description 7
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
239000003093 cationic surfactant Substances 0.000 description 6
125000004432 carbon atom Chemical group C* 0.000 description 5
125000002843 carboxylic acid group Chemical group 0.000 description 5
238000009472 formulation Methods 0.000 description 5
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 5
239000002736 nonionic surfactant Substances 0.000 description 5
229940027983 antiseptic and disinfectant quaternary ammonium compound Drugs 0.000 description 4
150000001875 compounds Chemical class 0.000 description 4
229940052303 ethers for general anesthesia Drugs 0.000 description 4
ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 3
POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 3
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 3
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
125000002877 alkyl aryl group Chemical group 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
229910052573 porcelain Inorganic materials 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000007921 spray Substances 0.000 description 3
ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 3
QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
125000002947 alkylene group Chemical group 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
229940093476 ethylene glycol Drugs 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
230000002209 hydrophobic effect Effects 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
239000007788 liquid Substances 0.000 description 2
239000000178 monomer Substances 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
150000003138 primary alcohols Chemical class 0.000 description 2
150000003242 quaternary ammonium salts Chemical class 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
YGKOYVNJPRSSRX-UHFFFAOYSA-M (4-dodecylphenyl)methyl-trimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCC1=CC=C(C[N+](C)(C)C)C=C1 YGKOYVNJPRSSRX-UHFFFAOYSA-M 0.000 description 1
GQNZWGIEBRBTOZ-UHFFFAOYSA-N (hexadecylamino)methyl-dimethyl-phenylazanium Chemical compound CCCCCCCCCCCCCCCCNC[N+](C)(C)C1=CC=CC=C1 GQNZWGIEBRBTOZ-UHFFFAOYSA-N 0.000 description 1
MWGRRMQNSQNFID-UHFFFAOYSA-N 1-(2-methylpropoxy)propan-2-ol Chemical compound CC(C)COCC(C)O MWGRRMQNSQNFID-UHFFFAOYSA-N 0.000 description 1
RWNUSVWFHDHRCJ-UHFFFAOYSA-N 1-butoxypropan-2-ol Chemical compound CCCCOCC(C)O RWNUSVWFHDHRCJ-UHFFFAOYSA-N 0.000 description 1
RRQYJINTUHWNHW-UHFFFAOYSA-N 1-ethoxy-2-(2-ethoxyethoxy)ethane Chemical compound CCOCCOCCOCC RRQYJINTUHWNHW-UHFFFAOYSA-N 0.000 description 1
JOLQKTGDSGKSKJ-UHFFFAOYSA-N 1-ethoxypropan-2-ol Chemical compound CCOCC(C)O JOLQKTGDSGKSKJ-UHFFFAOYSA-N 0.000 description 1
OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
CUDYYMUUJHLCGZ-UHFFFAOYSA-N 2-(2-methoxypropoxy)propan-1-ol Chemical compound COC(C)COC(C)CO CUDYYMUUJHLCGZ-UHFFFAOYSA-N 0.000 description 1
ZUAURMBNZUCEAF-UHFFFAOYSA-N 2-(2-phenoxyethoxy)ethanol Chemical compound OCCOCCOC1=CC=CC=C1 ZUAURMBNZUCEAF-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
WAEVWDZKMBQDEJ-UHFFFAOYSA-N 2-[2-(2-methoxypropoxy)propoxy]propan-1-ol Chemical compound COC(C)COC(C)COC(C)CO WAEVWDZKMBQDEJ-UHFFFAOYSA-N 0.000 description 1
URDCARMUOSMFFI-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]ethyl-(2-hydroxyethyl)amino]acetic acid Chemical compound OCCN(CC(O)=O)CCN(CC(O)=O)CC(O)=O URDCARMUOSMFFI-UHFFFAOYSA-N 0.000 description 1
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
QCAHUFWKIQLBNB-UHFFFAOYSA-N 3-(3-methoxypropoxy)propan-1-ol Chemical compound COCCCOCCCO QCAHUFWKIQLBNB-UHFFFAOYSA-N 0.000 description 1
LDMRLRNXHLPZJN-UHFFFAOYSA-N 3-propoxypropan-1-ol Chemical compound CCCOCCCO LDMRLRNXHLPZJN-UHFFFAOYSA-N 0.000 description 1
241000894006 Bacteria Species 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
229920004518 DION® Polymers 0.000 description 1
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
241000192125 Firmicutes Species 0.000 description 1
QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 1
PVTDRWOKWUJOIU-UHFFFAOYSA-M [ethoxy-(2-octylphenyl)-phenoxymethyl]-ethyl-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCC1=CC=CC=C1C(OCC)([N+](C)(C)CC)OC1=CC=CC=C1 PVTDRWOKWUJOIU-UHFFFAOYSA-M 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
125000004171 alkoxy aryl group Chemical group 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
150000001346 alkyl aryl ethers Chemical class 0.000 description 1
150000001450 anions Chemical class 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
125000004104 aryloxy group Chemical group 0.000 description 1
238000003287 bathing Methods 0.000 description 1
UREZNYTWGJKWBI-UHFFFAOYSA-M benzethonium chloride Chemical compound [Cl-].C1=CC(C(C)(C)CC(C)(C)C)=CC=C1OCCOCC[N+](C)(C)CC1=CC=CC=C1 UREZNYTWGJKWBI-UHFFFAOYSA-M 0.000 description 1
VZWMKHUMEIECPK-UHFFFAOYSA-M benzyl-dimethyl-octadecylazanium;bromide Chemical compound [Br-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 VZWMKHUMEIECPK-UHFFFAOYSA-M 0.000 description 1
XIWFQDBQMCDYJT-UHFFFAOYSA-M benzyl-dimethyl-tridecylazanium;chloride Chemical class [Cl-].CCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 XIWFQDBQMCDYJT-UHFFFAOYSA-M 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
239000003518 caustics Substances 0.000 description 1
239000000919 ceramic Substances 0.000 description 1
DVBJBNKEBPCGSY-UHFFFAOYSA-M cetylpyridinium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 DVBJBNKEBPCGSY-UHFFFAOYSA-M 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
235000015165 citric acid Nutrition 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
239000008367 deionised water Substances 0.000 description 1
229910021641 deionized water Inorganic materials 0.000 description 1
210000003298 dental enamel Anatomy 0.000 description 1
239000000645 desinfectant Substances 0.000 description 1
229940019778 diethylene glycol diethyl ether Drugs 0.000 description 1
229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
KOEHFKDKKINDQG-UHFFFAOYSA-N dimethyl-phenyl-tridecylazanium Chemical compound CCCCCCCCCCCCC[N+](C)(C)C1=CC=CC=C1 KOEHFKDKKINDQG-UHFFFAOYSA-N 0.000 description 1
238000002845 discoloration Methods 0.000 description 1
LHGPSNLCXCBBLU-UHFFFAOYSA-M dodecoxymethyl-dimethyl-phenylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCOC[N+](C)(C)C1=CC=CC=C1 LHGPSNLCXCBBLU-UHFFFAOYSA-M 0.000 description 1
SYELZBGXAIXKHU-UHFFFAOYSA-N dodecyldimethylamine N-oxide Chemical compound CCCCCCCCCCCC[N+](C)(C)[O-] SYELZBGXAIXKHU-UHFFFAOYSA-N 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
238000009408 flooring Methods 0.000 description 1
150000004820 halides Chemical group 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
239000004579 marble Substances 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
125000004433 nitrogen atom Chemical group N* 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
229960003330 pentetic acid Drugs 0.000 description 1
MFICKYHNFWASBT-UHFFFAOYSA-N phenol;propane-1,2-diol Chemical compound CC(O)CO.OC1=CC=CC=C1 MFICKYHNFWASBT-UHFFFAOYSA-N 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000000047 product Substances 0.000 description 1
LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
239000011819 refractory material Substances 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
150000003333 secondary alcohols Chemical class 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000008399 tap water Substances 0.000 description 1
235000020679 tap water Nutrition 0.000 description 1
150000003509 tertiary alcohols Chemical class 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
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/044—Hydroxides or bases
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/835—Mixtures of non-ionic with cationic compounds
- 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
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/10—Carbonates ; Bicarbonates
- 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
- C11D3/2068—Ethers
- 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
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/62—Quaternary ammonium compounds
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/75—Amino oxides

Landscapes

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)
Inorganic Chemistry (AREA)
Health & Medical Sciences (AREA)
Emergency Medicine (AREA)
Detergent Compositions (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

ZA200304587A 2000-12-15 2003-06-12 Alkaline cleaning and sanitizing composition effective for soap scum removal. ZA200304587B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB0030608A GB2370042A (en)	2000-12-15	2000-12-15	Hard surface cleaning compositions

Publications (1)

Publication Number	Publication Date
ZA200304587B true ZA200304587B (en)	2004-06-25

Family

ID=9905150

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ZA200304587A ZA200304587B (en)	2000-12-15	2003-06-12	Alkaline cleaning and sanitizing composition effective for soap scum removal.

Country Status (15)

Country	Link
US (2)	US6750190B2 (de)
EP (1)	EP1349910B1 (de)
CN (1)	CN1237161C (de)
AR (1)	AR031806A1 (de)
AT (1)	ATE307183T1 (de)
AU (1)	AU2002223079A1 (de)
BR (1)	BR0116170A (de)
CA (1)	CA2431741A1 (de)
DE (1)	DE60114235T2 (de)
ES (1)	ES2247003T3 (de)
GB (1)	GB2370042A (de)
MX (1)	MXPA03005309A (de)
PL (1)	PL204843B1 (de)
WO (1)	WO2002048299A1 (de)
ZA (1)	ZA200304587B (de)

Families Citing this family (39)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB2370042A (en)	2000-12-15	2002-06-19	Reckitt Benckiser Inc	Hard surface cleaning compositions
US6838421B2 (en) *	2003-05-19	2005-01-04	Colgate-Palmolive Company	Bathroom cleaning composition
CA2602377C (en) *	2005-04-13	2013-09-24	Unilever Plc	Liquid hard surface cleaning composition
EP1965756A2 (de) *	2005-12-30	2008-09-10	The Dial Corporation	Antibakterielle zusammensetzungen mit quaternären ammoniak-germiziden und alkamin-oxiden mit reduziertem reizpotential
US20090099057A1 (en) *	2006-03-03	2009-04-16	Reckitt Benckiser, Inc.	Hard Surface Cleaning Composition
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2000
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2001
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- 2001-11-19 CA CA002431741A patent/CA2431741A1/en not_active Abandoned
- 2001-11-19 ES ES01270588T patent/ES2247003T3/es not_active Expired - Lifetime
- 2001-11-19 AT AT01270588T patent/ATE307183T1/de not_active IP Right Cessation
- 2001-11-19 PL PL363373A patent/PL204843B1/pl not_active IP Right Cessation
- 2001-11-19 WO PCT/GB2001/005120 patent/WO2002048299A1/en not_active Ceased
- 2001-11-19 MX MXPA03005309A patent/MXPA03005309A/es not_active Application Discontinuation
- 2001-11-19 EP EP01270588A patent/EP1349910B1/de not_active Expired - Lifetime
- 2001-11-19 US US10/450,219 patent/US6750190B2/en not_active Expired - Lifetime
- 2001-11-19 BR BR0116170-9A patent/BR0116170A/pt not_active Application Discontinuation
- 2001-11-19 DE DE60114235T patent/DE60114235T2/de not_active Expired - Lifetime
- 2001-11-19 CN CNB018204325A patent/CN1237161C/zh not_active Expired - Fee Related
- 2001-12-12 AR ARP010105791A patent/AR031806A1/es unknown
2003
- 2003-06-12 ZA ZA200304587A patent/ZA200304587B/en unknown
2004
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Also Published As

Publication number	Publication date
DE60114235T2 (de)	2006-07-27
CN1237161C (zh)	2006-01-18
US6933267B2 (en)	2005-08-23
PL363373A1 (en)	2004-11-15
DE60114235D1 (de)	2006-03-02
WO2002048299A1 (en)	2002-06-20
US20040072711A1 (en)	2004-04-15
US6750190B2 (en)	2004-06-15
CN1479781A (zh)	2004-03-03
US20040224867A1 (en)	2004-11-11
GB0030608D0 (en)	2001-01-31
GB2370042A (en)	2002-06-19
BR0116170A (pt)	2003-11-11
AU2002223079A1 (en)	2002-06-24
ATE307183T1 (de)	2005-11-15
EP1349910B1 (de)	2005-10-19
AR031806A1 (es)	2003-10-01
CA2431741A1 (en)	2002-06-20
EP1349910A1 (de)	2003-10-08
PL204843B1 (pl)	2010-02-26
ES2247003T3 (es)	2006-03-01
MXPA03005309A (es)	2004-04-05

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