CA2254947A1 - Detergent composition - Google Patents

Detergent composition Download PDF

Info

Publication number: CA2254947A1
Authority: CA; Canada
Prior art keywords: aqa; bis; surfactant; compositions; bleach
Prior art date: 1996-05-17
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.): Abandoned

Application number

CA002254947A

Other languages

English (en)

French (fr)

Inventor

Kaori Asano

Jeffrey John Scheibel

Kaori Minamikawa

Laura Cron

Jean-Luc Bettiol

Thomas Anthony Cripe

John Downing Curry

Kevin Lee Kott

Ian Martin Dodd

Richard Timothy Hartshorn

Christiaan Arthur Jacques Kamiel Thoen

Rinko Katsuda

Frank Andrej Kvietok

Mark Hsiang-Kuen Mao

Michael Alan John Moss

Susumu Murata

Peter Robert Foley

Rajan Keshav Panandiker

Kakumanu Pramod

Khizar Mohamed Khan Sarnaik

Kenneth William Willman

Sanjeev Krishnadas Manohar

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Procter and Gamble Co

Original Assignee

Individual

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.)

1996-05-17

Filing date

1997-05-16

Publication date

1997-11-27

1997-05-16 Application filed by Individual filed Critical Individual

1997-11-27 Publication of CA2254947A1 publication Critical patent/CA2254947A1/en

Status Abandoned legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 229
239000003599 detergent Substances 0.000 title claims abstract description 15
239000007844 bleaching agent Substances 0.000 claims abstract description 82
239000004094 surface-active agent Substances 0.000 claims abstract description 80
239000012190 activator Substances 0.000 claims abstract description 34
239000003093 cationic surfactant Substances 0.000 claims abstract description 14
125000001453 quaternary ammonium group Chemical group 0.000 claims abstract description 3
239000002689 soil Substances 0.000 claims description 70
239000007788 liquid Substances 0.000 claims description 55
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 51
239000004744 fabric Substances 0.000 claims description 32
125000000217 alkyl group Chemical group 0.000 claims description 31
239000004615 ingredient Substances 0.000 claims description 27
238000000034 method Methods 0.000 claims description 26
125000002091 cationic group Chemical group 0.000 claims description 22
239000003945 anionic surfactant Substances 0.000 claims description 16
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 13
239000002304 perfume Substances 0.000 claims description 12
150000001450 anions Chemical group 0.000 claims description 11
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 8
229910052739 hydrogen Inorganic materials 0.000 claims description 8
125000003118 aryl group Chemical group 0.000 claims description 7
239000001257 hydrogen Substances 0.000 claims description 7
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 6
125000003342 alkenyl group Chemical group 0.000 claims description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
125000002877 alkyl aryl group Chemical group 0.000 claims description 4
MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 claims description 4
125000001033 ether group Chemical group 0.000 claims description 3
238000002156 mixing Methods 0.000 claims description 3
JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical class [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 claims description 3
125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 3
JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 claims description 2
230000008021 deposition Effects 0.000 claims description 2
125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 1
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
239000012736 aqueous medium Substances 0.000 claims 1
230000002708 enhancing effect Effects 0.000 claims 1
125000005342 perphosphate group Chemical group 0.000 claims 1
ZRXJXIVOMZDPKQ-UHFFFAOYSA-N phenyl 6-(nonanoylamino)hexanoate Chemical compound CCCCCCCCC(=O)NCCCCCC(=O)OC1=CC=CC=C1 ZRXJXIVOMZDPKQ-UHFFFAOYSA-N 0.000 claims 1
FRPJTGXMTIIFIT-UHFFFAOYSA-N tetraacetylethylenediamine Chemical group CC(=O)C(N)(C(C)=O)C(N)(C(C)=O)C(C)=O FRPJTGXMTIIFIT-UHFFFAOYSA-N 0.000 claims 1
-1 amino- Chemical class 0.000 description 94
239000000047 product Substances 0.000 description 56
239000000463 material Substances 0.000 description 55
239000003795 chemical substances by application Substances 0.000 description 50
239000011734 sodium Substances 0.000 description 46
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235000019441 ethanol Nutrition 0.000 description 38
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 37
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 37
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 33
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 32
239000007791 liquid phase Substances 0.000 description 31
239000000243 solution Substances 0.000 description 31
108010065511 Amylases Proteins 0.000 description 30
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239000002253 acid Substances 0.000 description 30
235000019418 amylase Nutrition 0.000 description 30
125000004432 carbon atom Chemical group C* 0.000 description 30
229920001223 polyethylene glycol Polymers 0.000 description 27
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 26
125000000129 anionic group Chemical group 0.000 description 26
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150000002500 ions Chemical class 0.000 description 26
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239000004367 Lipase Substances 0.000 description 25
150000001412 amines Chemical class 0.000 description 25
150000002148 esters Chemical class 0.000 description 25
235000019421 lipase Nutrition 0.000 description 25
238000006243 chemical reaction Methods 0.000 description 24
239000003054 catalyst Substances 0.000 description 23
239000002245 particle Substances 0.000 description 23
229920000642 polymer Polymers 0.000 description 22
239000002202 Polyethylene glycol Substances 0.000 description 21
229920001296 polysiloxane Polymers 0.000 description 21
238000005406 washing Methods 0.000 description 21
229940025131 amylases Drugs 0.000 description 20
150000001875 compounds Chemical class 0.000 description 20
239000010457 zeolite Substances 0.000 description 19
IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 description 18
230000000694 effects Effects 0.000 description 18
239000002904 solvent Substances 0.000 description 18
108091005804 Peptidases Proteins 0.000 description 17
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239000003085 diluting agent Substances 0.000 description 17
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 17
238000004851 dishwashing Methods 0.000 description 17
239000004382 Amylase Substances 0.000 description 16
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 15
230000002209 hydrophobic effect Effects 0.000 description 15
238000012360 testing method Methods 0.000 description 15
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 14
235000014113 dietary fatty acids Nutrition 0.000 description 14
239000000975 dye Substances 0.000 description 14
239000000194 fatty acid Substances 0.000 description 14
229930195729 fatty acid Natural products 0.000 description 14
239000004365 Protease Substances 0.000 description 13
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 13
229910052783 alkali metal Inorganic materials 0.000 description 13
238000004140 cleaning Methods 0.000 description 13
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 13
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 12
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
239000004927 clay Substances 0.000 description 12
239000008187 granular material Substances 0.000 description 12
229920005646 polycarboxylate Polymers 0.000 description 12
239000007787 solid Substances 0.000 description 12
MHKLKWCYGIBEQF-UHFFFAOYSA-N 4-(1,3-benzothiazol-2-ylsulfanyl)morpholine Chemical compound C1COCCN1SC1=NC2=CC=CC=C2S1 MHKLKWCYGIBEQF-UHFFFAOYSA-N 0.000 description 11
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 11
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 11
239000000460 chlorine Substances 0.000 description 11
229910052801 chlorine Inorganic materials 0.000 description 11
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 11
238000004900 laundering Methods 0.000 description 11
239000000377 silicon dioxide Substances 0.000 description 11
241000894007 species Species 0.000 description 11
239000002585 base Substances 0.000 description 10
230000015572 biosynthetic process Effects 0.000 description 10
150000004665 fatty acids Chemical class 0.000 description 10
150000002191 fatty alcohols Chemical class 0.000 description 10
230000003287 optical effect Effects 0.000 description 10
239000011236 particulate material Substances 0.000 description 10
230000008569 process Effects 0.000 description 10
229910052938 sodium sulfate Inorganic materials 0.000 description 10
235000011152 sodium sulphate Nutrition 0.000 description 10
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 9
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 9
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 9
150000001298 alcohols Chemical class 0.000 description 9
150000001340 alkali metals Chemical class 0.000 description 9
230000008901 benefit Effects 0.000 description 9
150000001768 cations Chemical class 0.000 description 9
238000007046 ethoxylation reaction Methods 0.000 description 9
239000003921 oil Substances 0.000 description 9
235000019198 oils Nutrition 0.000 description 9
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SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 8
SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 8
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GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 8
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BGRWYDHXPHLNKA-UHFFFAOYSA-N Tetraacetylethylenediamine Chemical compound CC(=O)N(C(C)=O)CCN(C(C)=O)C(C)=O BGRWYDHXPHLNKA-UHFFFAOYSA-N 0.000 description 8
239000000654 additive Substances 0.000 description 8
239000011575 calcium Substances 0.000 description 8
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YGUMVDWOQQJBGA-VAWYXSNFSA-N 5-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-[(e)-2-[4-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound C=1C=C(\C=C\C=2C(=CC(NC=3N=C(N=C(NC=4C=CC=CC=4)N=3)N3CCOCC3)=CC=2)S(O)(=O)=O)C(S(=O)(=O)O)=CC=1NC(N=C(N=1)N2CCOCC2)=NC=1NC1=CC=CC=C1 YGUMVDWOQQJBGA-VAWYXSNFSA-N 0.000 description 7
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IOVGROKTTNBUGK-SJCJKPOMSA-N ritodrine Chemical compound N([C@@H](C)[C@H](O)C=1C=CC(O)=CC=1)CCC1=CC=C(O)C=C1 IOVGROKTTNBUGK-SJCJKPOMSA-N 0.000 description 1
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FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 1
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HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
229940001584 sodium metabisulfite Drugs 0.000 description 1
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235000010339 sodium tetraborate Nutrition 0.000 description 1
FQUAWOQWQIVZLB-UHFFFAOYSA-M sodium;2-(2,3-dihydroxypropoxy)ethanesulfonate Chemical compound [Na+].OCC(O)COCCS([O-])(=O)=O FQUAWOQWQIVZLB-UHFFFAOYSA-M 0.000 description 1
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239000011550 stock solution Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
239000001384 succinic acid Substances 0.000 description 1
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DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 1
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150000003626 triacylglycerols Chemical class 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
125000005591 trimellitate group Chemical group 0.000 description 1
UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 1
RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
OHOTVSOGTVKXEL-UHFFFAOYSA-K trisodium;2-[bis(carboxylatomethyl)amino]propanoate Chemical class [Na+].[Na+].[Na+].[O-]C(=O)C(C)N(CC([O-])=O)CC([O-])=O OHOTVSOGTVKXEL-UHFFFAOYSA-K 0.000 description 1
229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
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229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1
FUQAYSQLAOJBBC-PAPYEOQZSA-N β-caryophyllene alcohol Chemical compound C1C[C@](C2)(C)CCC[C@]2(O)[C@H]2CC(C)(C)[C@@H]21 FUQAYSQLAOJBBC-PAPYEOQZSA-N 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
- C11D3/042—Acids
- 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
- C11D1/38—Cationic compounds
- C11D1/65—Mixtures of anionic 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
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0036—Soil deposition preventing compositions; Antiredeposition agents
- 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
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0052—Gas evolving or heat producing 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
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0063—Photo- activating 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
- C11D3/06—Phosphates, including polyphosphates
- 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
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—Water-insoluble compounds
- C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
- C11D3/1246—Silicates, e.g. diatomaceous earth
- C11D3/1253—Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite
- C11D3/1273—Crystalline layered silicates of type NaMeSixO2x+1YH2O
- 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
- C11D3/12—Water-insoluble compounds
- C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
- C11D3/1246—Silicates, e.g. diatomaceous earth
- C11D3/128—Aluminium silicates, e.g. zeolites
- 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
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3715—Polyesters or polycarbonates
- 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
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3723—Polyamines or polyalkyleneimines
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/386—Preparations containing enzymes, e.g. protease or amylase
- 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
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3902—Organic or inorganic per-compounds combined with specific additives
- C11D3/3905—Bleach activators or bleach catalysts
- C11D3/3907—Organic 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
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3902—Organic or inorganic per-compounds combined with specific additives
- C11D3/3905—Bleach activators or bleach catalysts
- C11D3/3932—Inorganic compounds or complexes
- 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
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3942—Inorganic per-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
- C11D3/40—Dyes ; Pigments
- C11D3/42—Brightening agents ; Blueing agents
- 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
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
- D06L4/60—Optical bleaching or brightening
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/005—Compositions containing perfumes; Compositions containing deodorants
- 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
- C11D1/02—Anionic 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
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/143—Sulfonic acid esters
- 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
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/146—Sulfuric acid esters
- 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
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic 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
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/29—Sulfates of polyoxyalkylene 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/40—Monoamines or polyamines; 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/42—Amino alcohols or amino ethers
- C11D1/44—Ethers of polyoxyalkylenes with amino alcohols; Condensation products of epoxyalkanes with amines

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Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Life Sciences & Earth Sciences (AREA)
Inorganic Chemistry (AREA)
Textile Engineering (AREA)
Health & Medical Sciences (AREA)
Emergency Medicine (AREA)
Crystallography & Structural Chemistry (AREA)
Detergent Compositions (AREA)

CA002254947A 1996-05-17 1997-05-16 Detergent composition Abandoned CA2254947A1 (en)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
US1788396P	1996-05-17	1996-05-17
US60/017,883		1996-05-17
PCT/US1997/008315 WO1997044431A1 (en)	1996-05-17	1997-05-16	Detergent composition

Publications (1)

Publication Number	Publication Date
CA2254947A1 true CA2254947A1 (en)	1997-11-27

Family

ID=21785076

Family Applications (8)

Application Number	Title	Priority Date	Filing Date
CA002254820A Abandoned CA2254820A1 (en)	1996-05-17	1997-05-16	Detergent composition
CA002255006A Abandoned CA2255006A1 (en)	1996-05-17	1997-05-16	Detergent composition
CA002255005A Abandoned CA2255005A1 (en)	1996-05-17	1997-05-16	Detergent composition
CA002254818A Abandoned CA2254818A1 (en)	1996-05-17	1997-05-16	Detergent composition
CA002255003A Abandoned CA2255003A1 (en)	1996-05-17	1997-05-16	Detergent composition
CA002254948A Abandoned CA2254948A1 (en)	1996-05-17	1997-05-16	Detergent composition
CA002254961A Abandoned CA2254961A1 (en)	1996-05-17	1997-05-16	Detergent composition
CA002254947A Abandoned CA2254947A1 (en)	1996-05-17	1997-05-16	Detergent composition

Family Applications Before (7)

Application Number	Title	Priority Date	Filing Date
CA002254820A Abandoned CA2254820A1 (en)	1996-05-17	1997-05-16	Detergent composition
CA002255006A Abandoned CA2255006A1 (en)	1996-05-17	1997-05-16	Detergent composition
CA002255005A Abandoned CA2255005A1 (en)	1996-05-17	1997-05-16	Detergent composition
CA002254818A Abandoned CA2254818A1 (en)	1996-05-17	1997-05-16	Detergent composition
CA002255003A Abandoned CA2255003A1 (en)	1996-05-17	1997-05-16	Detergent composition
CA002254948A Abandoned CA2254948A1 (en)	1996-05-17	1997-05-16	Detergent composition
CA002254961A Abandoned CA2254961A1 (en)	1996-05-17	1997-05-16	Detergent composition

Country Status (9)

Country	Link
EP (7)	EP0906403A1 (pt)
JP (8)	JPH11510554A (pt)
CN (6)	CN1225677A (pt)
AR (2)	AR007169A1 (pt)
BR (8)	BR9710445A (pt)
CA (8)	CA2254820A1 (pt)
MX (8)	MX9809679A (pt)
WO (8)	WO1997044418A1 (pt)
ZA (1)	ZA974226B (pt)

Families Citing this family (46)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
ZA974226B (en) *	1996-05-17	1998-12-28	Procter & Gamble	Detergent composition
MA25183A1 (fr) *	1996-05-17	2001-07-02	Arthur Jacques Kami Christiaan	Compositions detergentes
DE19824687A1 (de) *	1998-06-03	1999-12-09	Henkel Kgaa	Amylase und Acetonitril-Derivate enthaltende Wasch- und Reinigungsmittel
DE69935001T2 (de) *	1998-11-02	2007-08-30	The Procter & Gamble Company, Cincinnati	Verwendung von polymeren in stoffbehandlungsmitteln mit reduzierter gewebe-abreibung
GB2348434A (en) *	1999-04-01	2000-10-04	Procter & Gamble	Detergent compositions
US5994285A (en) *	1999-06-14	1999-11-30	Colgate-Palmolive Co.	Liquid laundry detergent composition containing ethoxylated amine quaternary surfactant
DE19948669A1 (de) *	1999-10-08	2001-04-19	Cognis Deutschland Gmbh	Waschmitteltabletten
DE19948668A1 (de) *	1999-10-08	2001-04-19	Cognis Deutschland Gmbh	Waschmitteltabletten
DE19948670A1 (de) *	1999-10-08	2001-04-19	Cognis Deutschland Gmbh	Waschmittel
WO2001034742A1 (en) *	1999-11-10	2001-05-17	Unilever Plc	Automatic dishwashing compositions containing water soluble cationic surfactants
WO2001034745A1 (en)	1999-11-10	2001-05-17	Unilever Plc	Automatic dishwashing compositions containing water soluble cationic surfactants
DE60024233T2 (de) *	2000-05-16	2006-07-20	Clariant International Limited	Verwendung kationischer Verbindungen
GB0021483D0 (en) *	2000-09-01	2000-10-18	Unilever Plc	Fabric care composition
DE10045289A1 (de) *	2000-09-13	2002-03-28	Henkel Kgaa	Schnell trocknendes Wasch- und Reinigungsmittel, insbesondere Handgeschirrspülmittel
US6638902B2 (en) *	2001-02-01	2003-10-28	Ecolab Inc.	Stable solid enzyme compositions and methods employing them
US6462014B1 (en)	2001-04-09	2002-10-08	Akzo Nobel N.V.	Low foaming/defoaming compositions containing alkoxylated quaternary ammonium compounds
JP2003129099A (ja) *	2001-10-24	2003-05-08	Kao Corp	衣料用粉末洗剤組成物
ES2258506T3 (es) *	2001-12-24	2006-09-01	Cognis Ip Management Gmbh	Composiciones cationicas para la limpieza de superficies duras.
ES2271529T3 (es) *	2002-02-25	2007-04-16	Ciba Specialty Chemicals Holding Inc.	Procedimiento para el tratamiento de materiales de fibra textil.
US20030228991A1 (en) *	2002-05-31	2003-12-11	Johnson Andress Kirsty	Premix compositions suitable for the preparation of aqueous or semi-aqueous cleaning and degreasing formulations with low VOCs.
EP1418226B1 (en) *	2002-11-07	2006-10-04	Unilever N.V.	Detergent composition
ES2391263T3 (es)	2002-12-04	2012-11-22	Clariant Finance (Bvi) Limited	Procedimiento para preparar una composición de amonio cuaternario
US8110537B2 (en) *	2003-01-14	2012-02-07	Ecolab Usa Inc.	Liquid detergent composition and methods for using
WO2006037438A1 (en) *	2004-10-04	2006-04-13	Unilever N.V.	Liquid detergent composition
JP2009537680A (ja) *	2006-05-23	2009-10-29	チバホールディングインコーポレーテッド	紡織繊維材料用洗剤組成物
JP2009149775A (ja) *	2007-12-20	2009-07-09	Lion Corp	洗濯槽用洗浄剤組成物
TW201031743A (en) *	2008-12-18	2010-09-01	Basf Se	Surfactant mixture comprising branched short-chain and branched long-chain components
JP5340821B2 (ja) *	2009-06-22	2013-11-13	三洋化成工業株式会社	台所用洗浄剤組成物
ES2548772T3 (es) *	2009-12-10	2015-10-20	The Procter & Gamble Company	Producto para lavavajillas y uso del mismo
EP2544810A2 (de) *	2010-03-10	2013-01-16	Basf Se	Verfahren zur erdölförderung unter verwendung von kationischen tensiden, die einen hydrophobblock mit einer kettenlänge von 6 bis 10 kohlenstoffatomen aufweisen
JP5642533B2 (ja) *	2010-12-24	2014-12-17	ライオン株式会社	自動食器洗い乾燥機用洗浄剤組成物
DE102012212728A1 (de) *	2012-07-19	2014-01-23	Henkel Ag & Co. Kgaa	Stabiles, flüssiges Waschmittel mit vergrauungsinhibierender Leistung II
AU2013357704B2 (en) *	2012-12-12	2016-07-07	Unilever Plc	Detergent composition
HUE043499T2 (hu) *	2013-03-28	2019-09-30	Procter & Gamble	Poliéteramin-tartalmú tiszítószerek
JP6184830B2 (ja) *	2013-06-14	2017-08-23	花王株式会社	漂白洗浄剤組成物
EP2915873A1 (en) *	2014-03-06	2015-09-09	The Procter and Gamble Company	Dishwashing composition
CN104059783B (zh) *	2014-06-10	2017-10-03	深圳市新纶科技股份有限公司	一种洗涤剂用表面活性剂的制备方法
EP3050955B2 (en) *	2015-02-02	2023-11-08	The Procter & Gamble Company	Detergent pack
JP6684558B2 (ja) *	2015-09-03	2020-04-22	ライオン株式会社	衣料用液体洗浄剤
JP6732424B2 (ja) *	2015-10-05	2020-07-29	花王株式会社	衣料用液体洗浄剤組成物
EP3301160A1 (en) *	2016-10-03	2018-04-04	The Procter & Gamble Company	Low ph laundry detergent composition
CN109983108A (zh) *	2016-11-24	2019-07-05	荷兰联合利华有限公司	液体洗涤剂组合物
CN112368362B (zh) *	2018-07-05	2022-05-24	赢创运营有限公司	用于高粘度洗衣清洁制剂的活性组合物
EP4053328A1 (de) *	2021-03-02	2022-09-07	CHT Germany GmbH	Kombinierte bleichbehandlung für textilien
CN118234837A (zh) *	2021-11-18	2024-06-21	埃科莱布美国股份有限公司	具有去污功能的用于锅碗瓢盆的手动洗涤剂
NL2032249B1 (nl) *	2022-06-22	2024-01-08	Hg Int B V	Samenstelling voor het verwijderen van kalkaanslag van gekleurd sanitair

Family Cites Families (42)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3668136A (en) *	1969-07-07	1972-06-06	Witco Chemical Corp	Compatible anionic-catonic surfactant compositions
US4033718A (en) *	1973-11-27	1977-07-05	The Procter & Gamble Company	Photoactivated bleaching process
BE40T1 (fr) *	1977-11-17	1980-01-11	Procter & Gamble	Compositions detergentes granulaires pour l'elimination ameliore des salissures graisseuses
CA1104451A (en) *	1978-02-28	1981-07-07	Manuel Juan De Luque	Detergent bleach composition and process
DE2967237D1 (en) *	1978-08-10	1984-10-31	Procter & Gamble Europ	Liquid detergent composition containing ternary surfactant system
JPS598392B2 (ja) *	1979-06-29	1984-02-24	花王株式会社	洗浄剤組成物
DE3064762D1 (en) *	1979-09-21	1983-10-13	Procter & Gamble	Washing and softening compositions and methods for their manufacture
EP0026529B2 (en) *	1979-09-29	1992-08-19	THE PROCTER & GAMBLE COMPANY	Detergent compositions
MX155643A (es) *	1980-02-29	1988-04-11	Ciba Geigy Ag	Composicion blanqueadora de telas
JPS5941672B2 (ja) *	1981-02-20	1984-10-08	花王株式会社	洗浄剤組成物
DE3366705D1 (en) *	1982-03-01	1986-11-13	Procter & Gamble	Detergent composition
JPS5959793A (ja) *	1982-09-30	1984-04-05	ライオン株式会社	粒状洗剤組成物
EP0108180B1 (fr) *	1982-11-05	1986-12-17	Reckitt & Colman S.A.	Compositions de rinçage pour le linge
DE3416472A1 (de) *	1984-05-04	1985-11-07	Hoechst Ag, 6230 Frankfurt	Weichmacher enthaltende waschmittel
GB8421800D0 (en) *	1984-08-29	1984-10-03	Unilever Plc	Detergent compositions
ZA862286B (en) *	1985-04-10	1987-11-25	Colgate Palmolive Co	Softening and anti-static nonionic detergent composition
EP0199403B1 (en) *	1985-04-15	1993-12-15	The Procter & Gamble Company	Stable liquid detergent compositions
ZA865751B (en) *	1985-08-20	1988-03-30	Colgate Palmolive Co	Built detergent compositions containing stabilizing agents
US4806260A (en) *	1986-02-21	1989-02-21	Colgate-Palmolive Company	Built nonaqueous liquid nonionic laundry detergent composition containing acid terminated nonionic surfactant and quarternary ammonium softener and method of use
GB8619153D0 (en) *	1986-08-06	1986-09-17	Unilever Plc	Fabric conditioning composition
US4704221A (en) *	1986-10-22	1987-11-03	The Procter & Gamble Company	Granular detergents which contain high levels of anionic surfactant that forms a middle-phase, surface treated with a water soluble cationic surfactant
EP0294893A3 (en) *	1987-06-10	1989-11-02	The Procter & Gamble Company	Conditioning agents and compositions containing same
US4913828A (en) *	1987-06-10	1990-04-03	The Procter & Gamble Company	Conditioning agents and compositions containing same
US4877896A (en) *	1987-10-05	1989-10-31	The Procter & Gamble Company	Sulfoaroyl end-capped ester of oligomers suitable as soil-release agents in detergent compositions and fabric-conditioner articles
GB8727659D0 (en) *	1987-11-26	1987-12-31	Unilever Plc	Machine dishwashing compositions
GB8900807D0 (en) *	1989-01-14	1989-03-08	British Petroleum Co Plc	Bleach compositions
US5441541A (en) *	1989-07-19	1995-08-15	Colgate Polmolive Co.	Anionic/cationic surfactant mixtures
US5290475A (en) *	1990-05-08	1994-03-01	Colgate Palmolive	Liquid softening and anti-static nonionic detergent composition with soil release promoting PET-POET copolymer
AU7633491A (en) *	1990-05-08	1991-11-14	Colgate-Palmolive Company, The	Liquid softening and anti-static nonionic detergent composition with soil release promoting pet-poet copolymer
ES2174820T3 (es) *	1991-01-16	2002-11-16	Procter & Gamble	Composiciones detergentes compactas con celulasa de alta actividad.
EP0495554A1 (en) *	1991-01-16	1992-07-22	The Procter & Gamble Company	Detergent compositions with high activity cellulase and quaternary ammonium compounds
JP2908589B2 (ja) *	1991-05-09	1999-06-21	花王株式会社	漂白剤及び漂白洗浄剤組成物
JP2974780B2 (ja) *	1992-02-18	1999-11-10	ザ、プロクター、エンド、ギャンブル、カンパニー	高活性セルラーゼと第四級アンモニウム化合物とを有する洗剤組成物
US5415807A (en) *	1993-07-08	1995-05-16	The Procter & Gamble Company	Sulfonated poly-ethoxy/propoxy end-capped ester oligomers suitable as soil release agents in detergent compositions
JP2813112B2 (ja) *	1993-08-30	1998-10-22	花王株式会社	衣料用液体洗浄剤組成物
US5466394A (en) *	1994-04-25	1995-11-14	The Procter & Gamble Co.	Stable, aqueous laundry detergent composition having improved softening properties
WO1995029217A1 (en) *	1994-04-25	1995-11-02	The Procter & Gamble Company	Stable, aqueous laundry detergent composition having improved softening properties
JPH07292389A (ja) *	1994-04-29	1995-11-07	Lion Corp	衣料用洗浄剤組成物
WO1995033033A1 (en) *	1994-06-01	1995-12-07	The Procter & Gamble Company	Laundry detergent compositions
EP0688859A1 (en) *	1994-06-22	1995-12-27	The Procter & Gamble Company	A process for treating textiles and compositions therefore
ZA974226B (en) *	1996-05-17	1998-12-28	Procter & Gamble	Detergent composition
MA25183A1 (fr) *	1996-05-17	2001-07-02	Arthur Jacques Kami Christiaan	Compositions detergentes

1997
- 1997-05-15 ZA ZA974226A patent/ZA974226B/xx unknown
- 1997-05-16 BR BR9710445A patent/BR9710445A/pt not_active Application Discontinuation
- 1997-05-16 WO PCT/US1997/008316 patent/WO1997044418A1/en not_active Application Discontinuation
- 1997-05-16 WO PCT/US1997/008314 patent/WO1997044425A2/en not_active Application Discontinuation
- 1997-05-16 CN CN97196468A patent/CN1225677A/zh active Pending
- 1997-05-16 AR ARP970102066A patent/AR007169A1/es unknown
- 1997-05-16 CA CA002254820A patent/CA2254820A1/en not_active Abandoned
- 1997-05-16 CA CA002255006A patent/CA2255006A1/en not_active Abandoned
- 1997-05-16 BR BR9710676A patent/BR9710676A/pt not_active Application Discontinuation
- 1997-05-16 CA CA002255005A patent/CA2255005A1/en not_active Abandoned
- 1997-05-16 CA CA002254818A patent/CA2254818A1/en not_active Abandoned
- 1997-05-16 CN CNB971964947A patent/CN1168812C/zh not_active Expired - Fee Related
- 1997-05-16 WO PCT/US1997/008373 patent/WO1997044433A1/en not_active Application Discontinuation
- 1997-05-16 EP EP97924742A patent/EP0906403A1/en not_active Withdrawn
- 1997-05-16 WO PCT/US1997/008444 patent/WO1997043388A2/en not_active Application Discontinuation
- 1997-05-16 BR BR9709321A patent/BR9709321A/pt not_active Application Discontinuation
- 1997-05-16 EP EP97925602A patent/EP0912669A2/en not_active Withdrawn
- 1997-05-16 JP JP9541172A patent/JPH11510554A/ja active Pending
- 1997-05-16 EP EP97926568A patent/EP0907705A1/en not_active Withdrawn
- 1997-05-16 WO PCT/US1997/008315 patent/WO1997044431A1/en not_active Application Discontinuation
- 1997-05-16 CA CA002255003A patent/CA2255003A1/en not_active Abandoned
- 1997-05-16 EP EP97924766A patent/EP0912686A2/en not_active Withdrawn
- 1997-05-16 WO PCT/US1997/008372 patent/WO1997044432A1/en not_active Application Discontinuation
- 1997-05-16 BR BR9709587-7A patent/BR9709587A/pt not_active Application Discontinuation
- 1997-05-16 CA CA002254948A patent/CA2254948A1/en not_active Abandoned
- 1997-05-16 JP JP9542571A patent/JPH11511794A/ja active Pending
- 1997-05-16 JP JP9542596A patent/JPH11511799A/ja active Pending
- 1997-05-16 JP JP9542574A patent/JPH11511797A/ja active Pending
- 1997-05-16 EP EP97924743A patent/EP0918833A1/en not_active Withdrawn
- 1997-05-16 CN CN97196481A patent/CN1225673A/zh active Pending
- 1997-05-16 BR BR9710675A patent/BR9710675A/pt not_active Application Discontinuation
- 1997-05-16 JP JP9542572A patent/JPH11511795A/ja active Pending
- 1997-05-16 WO PCT/US1997/008445 patent/WO1997043394A2/en active Application Filing
- 1997-05-16 AR ARP970102077A patent/AR014606A1/es unknown
- 1997-05-16 BR BR9710444A patent/BR9710444A/pt not_active Application Discontinuation
- 1997-05-16 BR BR9710667A patent/BR9710667A/pt not_active Application Discontinuation
- 1997-05-16 CN CN97196475A patent/CN1225678A/zh active Pending
- 1997-05-16 JP JP9542573A patent/JPH11511796A/ja active Pending
- 1997-05-16 JP JP9542597A patent/JP2000504061A/ja active Pending
- 1997-05-16 WO PCT/US1997/008317 patent/WO1997044419A2/en not_active Application Discontinuation
- 1997-05-16 CA CA002254961A patent/CA2254961A1/en not_active Abandoned
- 1997-05-16 JP JP9541173A patent/JPH11512782A/ja active Pending
- 1997-05-16 CA CA002254947A patent/CA2254947A1/en not_active Abandoned
- 1997-05-16 CN CN97196466A patent/CN1230213A/zh active Pending
- 1997-05-16 CN CN97196467A patent/CN1232489A/zh active Pending
- 1997-05-16 BR BR9710678A patent/BR9710678A/pt not_active Application Discontinuation
- 1997-05-16 EP EP97924741A patent/EP0906392A2/en not_active Withdrawn
- 1997-05-16 EP EP97927653A patent/EP0906405A1/en not_active Withdrawn
1998
- 1998-11-17 MX MX9809679A patent/MX9809679A/es unknown
- 1998-11-17 MX MX9809683A patent/MX9809683A/es unknown
- 1998-11-17 MX MX9809674A patent/MX9809674A/es unknown
- 1998-11-17 MX MX9809684A patent/MX9809684A/es unknown
- 1998-11-17 MX MX9809624A patent/MX9809624A/es unknown
- 1998-11-17 MX MX9809628A patent/MX9809628A/es unknown
- 1998-11-17 MX MX9809675A patent/MX9809675A/es unknown
- 1998-11-17 MX MX9809681A patent/MX9809681A/es unknown

Also Published As

Publication number	Publication date
EP0918833A1 (en)	1999-06-02
CA2254818A1 (en)	1997-11-27
BR9710445A (pt)	1999-08-17
CN1225673A (zh)	1999-08-11
CN1232489A (zh)	1999-10-20
EP0912686A2 (en)	1999-05-06
BR9710678A (pt)	1999-08-17
WO1997044425A3 (en)	1997-12-24
CA2255005A1 (en)	1997-11-20
JPH11511795A (ja)	1999-10-12
BR9709321A (pt)	1999-08-10
WO1997043388A2 (en)	1997-11-20
MX9809681A (es)	1999-03-01
MX9809679A (en)	1999-03-01
BR9710667A (pt)	1999-08-17
CN1225678A (zh)	1999-08-11
AR014606A1 (es)	2001-03-28
BR9710676A (pt)	1999-08-17
CN1168812C (zh)	2004-09-29
WO1997044419A2 (en)	1997-11-27
CA2254948A1 (en)	1997-11-27
JPH11510554A (ja)	1999-09-14
CA2254961A1 (en)	1997-11-27
JP2000504061A (ja)	2000-04-04
AR007169A1 (es)	1999-10-13
WO1997043394A2 (en)	1997-11-20
MX9809624A (en)	1999-03-01
CA2254820A1 (en)	1997-11-27
CA2255006A1 (en)	1997-11-20
MX9809683A (en)	1999-03-01
EP0906405A1 (en)	1999-04-07
WO1997043394A3 (en)	1997-12-24
EP0906403A1 (en)	1999-04-07
BR9709587A (pt)	2000-04-25
CA2255003A1 (en)	1997-11-27
CN1225675A (zh)	1999-08-11
JPH11512782A (ja)	1999-11-02
JPH11511797A (ja)	1999-10-12
BR9710444A (pt)	1999-08-17
MX9809674A (en)	1999-03-01
ZA974226B (en)	1998-12-28
MX9809684A (en)	1999-03-01
MX9809628A (en)	1999-02-01
JPH11511799A (ja)	1999-10-12
JPH11511796A (ja)	1999-10-12
WO1997044425A2 (en)	1997-11-27
BR9710675A (pt)	1999-08-17
MX9809675A (en)	1999-03-01
EP0907705A1 (en)	1999-04-14
CN1230213A (zh)	1999-09-29
JPH11511794A (ja)	1999-10-12
EP0912669A2 (en)	1999-05-06
WO1997043388A3 (en)	1998-02-12
WO1997044432A1 (en)	1997-11-27
WO1997044419A3 (en)	1997-12-31
WO1997044431A1 (en)	1997-11-27
EP0906392A2 (en)	1999-04-07
WO1997044418A1 (en)	1997-11-27
WO1997044433A1 (en)	1997-11-27
CN1225677A (zh)	1999-08-11

Legal Events

Date	Code	Title	Description
1998-11-17	EEER	Examination request
2002-05-16	FZDE	Dead

Publication	Publication Date	Title
CA2254947A1 (en)	1997-11-27	Detergent composition
US6136769A (en)	2000-10-24	Alkoxylated cationic detergency ingredients
CA2254955A1 (en)	1997-11-27	Detergent composition
GB2314339A (en)	1997-12-24	Cleaning compositions containing amido surfactants derived from amido furandiones
EP0996700A1 (en)	2000-05-03	Detergent compositions