EP3303536B1 - Laundry detergent composition - Google Patents

Laundry detergent composition Download PDF

Info

Publication number: EP3303536B1
Authority: EP; European Patent Office
Prior art keywords: laundry detergent; detergent composition; protease; composition according; alkoxylated
Prior art date: 2015-06-02
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.): Active

Application number

EP16718686.5A

Other languages

German (de)

English (en)

French (fr)

Other versions

EP3303536A1 (en

Inventor

Stephen Norman Batchelor

Jayne Michelle Bird

Dietmar Andreas LANG

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.)

Unilever PLC

Unilever NV

Original Assignee

Unilever PLC

Unilever NV

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.)

2015-06-02

Filing date

2016-04-26

Publication date

2019-04-17

2016-04-26 Application filed by Unilever PLC, Unilever NV filed Critical Unilever PLC

2018-04-11 Publication of EP3303536A1 publication Critical patent/EP3303536A1/en

2019-04-17 Application granted granted Critical

2019-04-17 Publication of EP3303536B1 publication Critical patent/EP3303536B1/en

Status Active legal-status Critical Current

2036-04-26 Anticipated expiration legal-status Critical

Links

239000000203 mixture Substances 0.000 title claims description 63
239000003599 detergent Substances 0.000 title claims description 35
-1 aryl phenol Chemical compound 0.000 claims description 46
108091005804 Peptidases Proteins 0.000 claims description 25
239000004365 Protease Substances 0.000 claims description 18
239000003945 anionic surfactant Substances 0.000 claims description 17
239000002736 nonionic surfactant Substances 0.000 claims description 14
239000004094 surface-active agent Substances 0.000 claims description 12
102000012479 Serine Proteases Human genes 0.000 claims description 10
108010022999 Serine Proteases Proteins 0.000 claims description 10
239000002270 dispersing agent Substances 0.000 claims description 9
239000004753 textile Substances 0.000 claims description 9
101710135785 Subtilisin-like protease Proteins 0.000 claims description 8
150000004996 alkyl benzenes Chemical class 0.000 claims description 7
125000000129 anionic group Chemical group 0.000 claims description 6
238000000034 method Methods 0.000 claims description 5
239000007864 aqueous solution Substances 0.000 claims description 4
239000007788 liquid Substances 0.000 claims description 4
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 3
238000005008 domestic process Methods 0.000 claims description 2
238000001035 drying Methods 0.000 claims description 2
239000000243 solution Substances 0.000 claims description 2
125000005504 styryl group Chemical group 0.000 claims description 2
102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 claims 4
150000005215 alkyl ethers Chemical class 0.000 claims 1
239000000975 dye Substances 0.000 description 30
102000035195 Peptidases Human genes 0.000 description 21
238000009472 formulation Methods 0.000 description 20
235000019419 proteases Nutrition 0.000 description 11
108090000787 Subtilisin Proteins 0.000 description 10
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 10
229910052708 sodium Inorganic materials 0.000 description 10
239000011734 sodium Substances 0.000 description 10
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 9
239000000463 material Substances 0.000 description 9
239000002304 perfume Substances 0.000 description 9
239000010457 zeolite Substances 0.000 description 9
101000740449 Bacillus subtilis (strain 168) Biotin/lipoyl attachment protein Proteins 0.000 description 8
229910021536 Zeolite Inorganic materials 0.000 description 8
VRVDFJOCCWSFLI-UHFFFAOYSA-K trisodium 3-[[4-[(6-anilino-1-hydroxy-3-sulfonatonaphthalen-2-yl)diazenyl]-5-methoxy-2-methylphenyl]diazenyl]naphthalene-1,5-disulfonate Chemical compound [Na+].[Na+].[Na+].COc1cc(N=Nc2cc(c3cccc(c3c2)S([O-])(=O)=O)S([O-])(=O)=O)c(C)cc1N=Nc1c(O)c2ccc(Nc3ccccc3)cc2cc1S([O-])(=O)=O VRVDFJOCCWSFLI-UHFFFAOYSA-K 0.000 description 8
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229910019142 PO4 Inorganic materials 0.000 description 6
YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 6
239000000987 azo dye Substances 0.000 description 6
229940088598 enzyme Drugs 0.000 description 6
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 6
239000010452 phosphate Substances 0.000 description 6
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 5
125000000217 alkyl group Chemical group 0.000 description 5
229910000323 aluminium silicate Inorganic materials 0.000 description 5
150000001875 compounds Chemical class 0.000 description 5
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 5
239000004744 fabric Substances 0.000 description 5
229910021653 sulphate ion Inorganic materials 0.000 description 5
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 4
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 4
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
229920002873 Polyethylenimine Polymers 0.000 description 4
150000001298 alcohols Chemical class 0.000 description 4
229910052783 alkali metal Inorganic materials 0.000 description 4
239000011575 calcium Substances 0.000 description 4
229910052791 calcium Inorganic materials 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
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VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 3
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KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
238000007046 ethoxylation reaction Methods 0.000 description 3
239000007850 fluorescent dye Substances 0.000 description 3
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125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
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XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
VEPOHXYIFQMVHW-XOZOLZJESA-N 2,3-dihydroxybutanedioic acid (2S,3S)-3,4-dimethyl-2-phenylmorpholine Chemical compound OC(C(O)C(O)=O)C(O)=O.C[C@H]1[C@@H](OCCN1C)c1ccccc1 VEPOHXYIFQMVHW-XOZOLZJESA-N 0.000 description 2
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BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 2
229920000742 Cotton Polymers 0.000 description 2
QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 2
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 2
241000579835 Merops Species 0.000 description 2
229910000503 Na-aluminosilicate Inorganic materials 0.000 description 2
PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 2
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
239000001000 anthraquinone dye Substances 0.000 description 2
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125000002091 cationic group Chemical group 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
235000019864 coconut oil Nutrition 0.000 description 2
239000003240 coconut oil Substances 0.000 description 2
239000008139 complexing agent Substances 0.000 description 2
239000002537 cosmetic Substances 0.000 description 2
229960001484 edetic acid Drugs 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 2
UWKAYLJWKGQEPM-LBPRGKRZSA-N linalyl acetate Chemical compound CC(C)=CCC[C@](C)(C=C)OC(C)=O UWKAYLJWKGQEPM-LBPRGKRZSA-N 0.000 description 2
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150000001408 amides Chemical class 0.000 description 1
235000019418 amylase Nutrition 0.000 description 1
229940025131 amylases Drugs 0.000 description 1
229940077388 benzenesulfonate Drugs 0.000 description 1
SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical class OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
230000008033 biological extinction Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000007844 bleaching agent Substances 0.000 description 1
239000008280 blood Substances 0.000 description 1
210000004369 blood Anatomy 0.000 description 1
239000004327 boric acid Substances 0.000 description 1
235000012745 brilliant blue FCF Nutrition 0.000 description 1
102220350531 c.80A>G Human genes 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000010500 citrus oil Substances 0.000 description 1
229910052681 coesite Inorganic materials 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
229910052593 corundum Inorganic materials 0.000 description 1
229910052906 cristobalite Inorganic materials 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
230000008021 deposition Effects 0.000 description 1
XSNQECSCDATQEL-UHFFFAOYSA-N dihydromyrcenol Chemical compound C=CC(C)CCCC(C)(C)O XSNQECSCDATQEL-UHFFFAOYSA-N 0.000 description 1
229930008394 dihydromyrcenol Natural products 0.000 description 1
239000001177 diphosphate Substances 0.000 description 1
XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 1
235000011180 diphosphates Nutrition 0.000 description 1
NJPXFJXCALXJCX-UHFFFAOYSA-L disodium 7-anilino-3-[[4-[(2,4-dimethyl-6-sulfonatophenyl)diazenyl]-2,5-dimethylphenyl]diazenyl]-4-hydroxynaphthalene-2-sulfonate Chemical compound [Na+].[Na+].Cc1cc(C)c(N=Nc2cc(C)c(cc2C)N=Nc2c(O)c3ccc(Nc4ccccc4)cc3cc2S([O-])(=O)=O)c(c1)S([O-])(=O)=O NJPXFJXCALXJCX-UHFFFAOYSA-L 0.000 description 1
LARMRMCFZNGNNX-UHFFFAOYSA-L disodium 7-anilino-3-[[4-[(2,4-dimethyl-6-sulfonatophenyl)diazenyl]-2-methoxy-5-methylphenyl]diazenyl]-4-hydroxynaphthalene-2-sulfonate Chemical compound [Na+].[Na+].COc1cc(N=Nc2c(C)cc(C)cc2S([O-])(=O)=O)c(C)cc1N=Nc1c(O)c2ccc(Nc3ccccc3)cc2cc1S([O-])(=O)=O LARMRMCFZNGNNX-UHFFFAOYSA-L 0.000 description 1
PMPJQLCPEQFEJW-HPKCLRQXSA-L disodium;2-[(e)-2-[4-[4-[(e)-2-(2-sulfonatophenyl)ethenyl]phenyl]phenyl]ethenyl]benzenesulfonate Chemical group [Na+].[Na+].[O-]S(=O)(=O)C1=CC=CC=C1\C=C\C1=CC=C(C=2C=CC(\C=C\C=3C(=CC=CC=3)S([O-])(=O)=O)=CC=2)C=C1 PMPJQLCPEQFEJW-HPKCLRQXSA-L 0.000 description 1
VUJGKADZTYCLIL-YHPRVSEPSA-L disodium;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-sulfonatophenyl]ethenyl]benzenesulfonate Chemical compound [Na+].[Na+].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 VUJGKADZTYCLIL-YHPRVSEPSA-L 0.000 description 1
VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 description 1
GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
238000004453 electron probe microanalysis Methods 0.000 description 1
230000002255 enzymatic effect Effects 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
SFNALCNOMXIBKG-UHFFFAOYSA-N ethylene glycol monododecyl ether Chemical compound CCCCCCCCCCCCOCCO SFNALCNOMXIBKG-UHFFFAOYSA-N 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000000835 fiber Substances 0.000 description 1
239000003205 fragrance Substances 0.000 description 1
239000008233 hard water Substances 0.000 description 1
125000000623 heterocyclic group Chemical group 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
125000001165 hydrophobic group Chemical group 0.000 description 1
CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
239000001102 lavandula vera Substances 0.000 description 1
235000018219 lavender Nutrition 0.000 description 1
229930007744 linalool Natural products 0.000 description 1
UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 description 1
235000019421 lipase Nutrition 0.000 description 1
238000005259 measurement Methods 0.000 description 1
108010003855 mesentericopeptidase Proteins 0.000 description 1
229910021645 metal ion Inorganic materials 0.000 description 1
108010009355 microbial metalloproteinases Proteins 0.000 description 1
235000013336 milk Nutrition 0.000 description 1
239000008267 milk Substances 0.000 description 1
210000004080 milk Anatomy 0.000 description 1
KJPHTXTWFHVJIG-UHFFFAOYSA-N n-ethyl-2-[(6-methoxypyridin-3-yl)-(2-methylphenyl)sulfonylamino]-n-(pyridin-3-ylmethyl)acetamide Chemical compound C=1C=C(OC)N=CC=1N(S(=O)(=O)C=1C(=CC=CC=1)C)CC(=O)N(CC)CC1=CC=CN=C1 KJPHTXTWFHVJIG-UHFFFAOYSA-N 0.000 description 1
ZOCHHNOQQHDWHG-UHFFFAOYSA-N n-hexan-3-ol Natural products CCCC(O)CC ZOCHHNOQQHDWHG-UHFFFAOYSA-N 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
230000003287 optical effect Effects 0.000 description 1
229960003330 pentetic acid Drugs 0.000 description 1
238000003359 percent control normalization Methods 0.000 description 1
150000004965 peroxy acids Chemical class 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
150000002988 phenazines Chemical class 0.000 description 1
HXITXNWTGFUOAU-UHFFFAOYSA-N phenylboronic acid Chemical class OB(O)C1=CC=CC=C1 HXITXNWTGFUOAU-UHFFFAOYSA-N 0.000 description 1
UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920002006 poly(N-vinylimidazole) polymer Polymers 0.000 description 1
229920000196 poly(lauryl methacrylate) Polymers 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920005646 polycarboxylate Polymers 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
239000001205 polyphosphate Substances 0.000 description 1
235000011176 polyphosphates Nutrition 0.000 description 1
229920005996 polystyrene-poly(ethylene-butylene)-polystyrene Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
150000003138 primary alcohols Chemical class 0.000 description 1
102000004196 processed proteins & peptides Human genes 0.000 description 1
238000012545 processing Methods 0.000 description 1
150000003219 pyrazolines Chemical class 0.000 description 1
KUIXZSYWBHSYCN-UHFFFAOYSA-L remazol brilliant blue r Chemical compound [Na+].[Na+].C1=C(S([O-])(=O)=O)C(N)=C2C(=O)C3=CC=CC=C3C(=O)C2=C1NC1=CC=CC(S(=O)(=O)CCOS([O-])(=O)=O)=C1 KUIXZSYWBHSYCN-UHFFFAOYSA-L 0.000 description 1
229930007790 rose oxide Natural products 0.000 description 1
102200131574 rs11556620 Human genes 0.000 description 1
102220036452 rs137882485 Human genes 0.000 description 1
102200065573 rs140660066 Human genes 0.000 description 1
102200118280 rs33918343 Human genes 0.000 description 1
102220243297 rs374524755 Human genes 0.000 description 1
102200034374 rs6092 Human genes 0.000 description 1
102220289974 rs757282628 Human genes 0.000 description 1
102200025035 rs786203989 Human genes 0.000 description 1
102220099575 rs878853725 Human genes 0.000 description 1
229940071207 sesquicarbonate Drugs 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
239000000344 soap Substances 0.000 description 1
229910001388 sodium aluminate Inorganic materials 0.000 description 1
239000000429 sodium aluminium silicate Substances 0.000 description 1
URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
229960001922 sodium perborate Drugs 0.000 description 1
229940045872 sodium percarbonate Drugs 0.000 description 1
NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
229910052911 sodium silicate Inorganic materials 0.000 description 1
235000019832 sodium triphosphate Nutrition 0.000 description 1
AXMCIYLNKNGNOT-UHFFFAOYSA-N sodium;3-[[4-[(4-dimethylazaniumylidenecyclohexa-2,5-dien-1-ylidene)-[4-[ethyl-[(3-sulfophenyl)methyl]amino]phenyl]methyl]-n-ethylanilino]methyl]benzenesulfonate Chemical compound [Na+].C=1C=C(C(=C2C=CC(C=C2)=[N+](C)C)C=2C=CC(=CC=2)N(CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S(O)(=O)=O)=C1 AXMCIYLNKNGNOT-UHFFFAOYSA-N 0.000 description 1
RBYJOOWYRXEJAM-UHFFFAOYSA-M sodium;5,9-dianilino-7-phenylbenzo[a]phenazin-7-ium-4,10-disulfonate Chemical compound [Na+].C=1C=CC=CC=1[N+]1=C2C=C(NC=3C=CC=CC=3)C(S(=O)(=O)[O-])=CC2=NC(C2=CC=CC(=C22)S([O-])(=O)=O)=C1C=C2NC1=CC=CC=C1 RBYJOOWYRXEJAM-UHFFFAOYSA-M 0.000 description 1
YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
241000894007 species Species 0.000 description 1
229910052682 stishovite Inorganic materials 0.000 description 1
239000000126 substance Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
239000000758 substrate Substances 0.000 description 1
150000005846 sugar alcohols Chemical class 0.000 description 1
125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
238000012360 testing method Methods 0.000 description 1
108010031354 thermitase Proteins 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
229910052905 tridymite Inorganic materials 0.000 description 1
239000001226 triphosphate Substances 0.000 description 1
235000011178 triphosphate Nutrition 0.000 description 1
UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 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
ZUCXUTRTSQLRCV-UHFFFAOYSA-K trisodium;1-amino-4-[3-[[4-chloro-6-(3-sulfonatoanilino)-1,3,5-triazin-2-yl]amino]-2,4,6-trimethyl-5-sulfonatoanilino]-9,10-dioxoanthracene-2-sulfonate Chemical compound [Na+].[Na+].[Na+].CC1=C(S([O-])(=O)=O)C(C)=C(NC=2C=3C(=O)C4=CC=CC=C4C(=O)C=3C(N)=C(C=2)S([O-])(=O)=O)C(C)=C1NC(N=1)=NC(Cl)=NC=1NC1=CC=CC(S([O-])(=O)=O)=C1 ZUCXUTRTSQLRCV-UHFFFAOYSA-K 0.000 description 1
VZPXDCIISFTYOM-UHFFFAOYSA-K trisodium;1-amino-4-[4-[[4-chloro-6-(3-sulfonatoanilino)-1,3,5-triazin-2-yl]amino]-3-sulfonatoanilino]-9,10-dioxoanthracene-2-sulfonate Chemical compound [Na+].[Na+].[Na+].C1=2C(=O)C3=CC=CC=C3C(=O)C=2C(N)=C(S([O-])(=O)=O)C=C1NC(C=C1S([O-])(=O)=O)=CC=C1NC(N=1)=NC(Cl)=NC=1NC1=CC=CC(S([O-])(=O)=O)=C1 VZPXDCIISFTYOM-UHFFFAOYSA-K 0.000 description 1
239000012588 trypsin Substances 0.000 description 1
238000005406 washing Methods 0.000 description 1
229910001845 yogo sapphire Inorganic materials 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/37—Mixtures of compounds all of which are anionic
- 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
- C11D1/83—Mixtures of non-ionic with 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
- 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
- C11D3/3707—Polyethers, e.g. polyalkyleneoxides
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/04—Carboxylic acids or salts thereof
- C11D1/06—Ether- or thioether carboxylic 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
- C11D1/02—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
- C11D1/02—Anionic compounds
- C11D1/34—Derivatives of acids of phosphorus
- C11D1/345—Phosphates or phosphites
- 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
- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
- C11D2111/10—Objects to be cleaned
- C11D2111/12—Soft surfaces, e.g. textile

Definitions

Protease enzymes are used in laundry detergent formulations to remove protein containing stains from fabrics.
amyloliquefaciens Bacillus pumilus and Bacillus gibsonii described in US7262042 and WO09/021867 , and subtilisin lentus, subtilisin Novo, subtilisin Carlsberg, Bacillus licheniformis, subtilisin BPN', subtilisin 309, subtilisin 147 and subtilisin 168 described in WO89/06279 and protease PD138 described in WO 93/18140 .
Other useful proteases may be those described in WO92/175177 , WO01/016285 , WO02/026024 and WO02/016547 .
trypsin-like proteases are trypsin (e.g.
two or more anionic surfactant are present, preferably linear alkyl benzene sulphonate together with an alkyl ether sulphate.
precipitating builder materials examples include sodium orthophosphate and sodium carbonate.
the laundry detergent formulation is a non-phosphate built laundry detergent formulation, i.e., contains less than 1 wt% of phosphate.
the powder laundry detergent formulation is carbonate built.
the composition preferably comprises a fluorescent agent (optical brightener).
fluorescent agents are well known and many such fluorescent agents are available commercially. Usually, these fluorescent agents are supplied and used in the form of their alkali metal salts, for example, the sodium salts.
the total amount of the fluorescent agent or agents used in the composition is generally from 0.005 to 2 wt %, more preferably 0.01 to 0.1 wt %.
Preferred classes of fluorescer are: Di-styryl biphenyl compounds, e.g. Tinopal (Trade Mark) CBS-X, Di-amine stilbene disulphonic acid compounds, e.g. Tinopal DMS pure Xtra and Blankophor (Trade Mark) HRH, and Pyrazoline compounds, e.g.
the composition comprises a perfume.
the perfume is preferably in the range from 0.001 to 3 wt %, most preferably 0.1 to 1 wt %.
CTFA Cosmetic, Toiletry and Fragrance Association

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)
Detergent Compositions (AREA)

EP16718686.5A 2015-06-02 2016-04-26 Laundry detergent composition Active EP3303536B1 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
EP15170341		2015-06-02
PCT/EP2016/059313 WO2016192905A1 (en)	2015-06-02	2016-04-26	Laundry detergent composition

Publications (2)

Publication Number	Publication Date
EP3303536A1 EP3303536A1 (en)	2018-04-11
EP3303536B1 true EP3303536B1 (en)	2019-04-17

Family

ID=53269413

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
EP16718686.5A Active EP3303536B1 (en)	2015-06-02	2016-04-26	Laundry detergent composition

Country Status (6)

Country	Link
EP (1)	EP3303536B1 (zh)
CN (1)	CN107835851B (zh)
AR (1)	AR104843A1 (zh)
BR (1)	BR112017025607B1 (zh)
TR (1)	TR201906836T4 (zh)
WO (1)	WO2016192905A1 (zh)

Family Cites Families (56)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2407980A1 (fr)	1977-11-02	1979-06-01	Rhone Poulenc Ind	Nouvelles compositions anti-salissure et anti-redeposition utilisables en detergence
US4760025A (en)	1984-05-29	1988-07-26	Genencor, Inc.	Modified enzymes and methods for making same
DK6488D0 (da)	1988-01-07	1988-01-07	Novo Industri As	Enzymer
DE68924654T2 (de)	1988-01-07	1996-04-04	Novonordisk As	Spezifische Protease.
CA2001927C (en)	1988-11-03	1999-12-21	Graham Thomas Brown	Aluminosilicates and detergent compositions
DK0493398T3 (da)	1989-08-25	2000-05-22	Henkel Research Corp	Alkalisk, proteolytisk enzym og fremgangsmåde til fremstilling deraf
DK58491D0 (da)	1991-04-03	1991-04-03	Novo Nordisk As	Hidtil ukendte proteaser
DE69209500T2 (de)	1991-04-30	1996-10-31	Procter & Gamble	Gerüstsubstanzhaltige flüssigwaschmittel mit borsäure-polyolkomplex zur ptoteolytischen enzyminhibierung
EP0511456A1 (en)	1991-04-30	1992-11-04	The Procter & Gamble Company	Liquid detergents with aromatic borate ester to inhibit proteolytic enzyme
DE69226182T2 (de)	1991-05-01	1999-01-21	Novo Nordisk As	Stabilisierte enzyme und waschmittelzusammensetzungen
DK28792D0 (da)	1992-03-04	1992-03-04	Novo Nordisk As	Nyt enzym
DK52393D0 (zh)	1993-05-05	1993-05-05	Novo Nordisk As
BR9407834A (pt)	1993-10-14	1997-05-13	Procter & Gamble	Composições de limpeza contendo protease
EP0824585B1 (en)	1995-05-05	2009-04-22	Novozymes A/S	Protease variants and compositions
US6300116B1 (en)	1996-11-04	2001-10-09	Novozymes A/S	Modified protease having improved autoproteolytic stability
EP0948610B1 (en)	1996-11-04	2011-05-25	Novozymes A/S	Subtilase variants and compositions
EP1009815B1 (en)	1997-08-29	2008-01-30	Novozymes A/S	Protease variants and compositions
AR015977A1 (es)	1997-10-23	2001-05-30	Genencor Int	Variantes de proteasa multiplemente substituida con carga neta alterada para su empleo en detergentes
NZ531394A (en)	1999-08-31	2005-10-28	Novozymes As	Residual protease II (RPII) and variants thereof useful in detergent compositions
WO2001044452A1 (en)	1999-12-15	2001-06-21	Novozymes A/S	Subtilase variants having an improved wash performance on egg stains
WO2002036727A1 (en) *	2000-01-14	2002-05-10	The Procter & Gamble Company	A detergent composition comprising a metallo protease and calcium ion
CN1337553A (zh)	2000-08-05	2002-02-27	李海泉	地下观光游乐园
CA2419896C (en)	2000-08-21	2014-12-09	Novozymes A/S	Subtilase enzymes
DK200101090A (da)	2001-07-12	2001-08-16	Novozymes As	Subtilase variants
DE10162728A1 (de)	2001-12-20	2003-07-10	Henkel Kgaa	Neue Alkalische Protease aus Bacillus gibsonii (DSM 14393) und Wasch-und Reinigungsmittel enthaltend diese neue Alkalische Protease
EP1520017A2 (en)	2002-06-26	2005-04-06	Novozymes A/S	Subtilases and subtilase variants having altered immunogenicity
US6911421B2 (en) *	2002-11-01	2005-06-28	Nicca Usa, Inc.	Surfactant blends for removing oligomer deposits from polyester fibers and polyester processing equipment
TWI319007B (en)	2002-11-06	2010-01-01	Novozymes As	Subtilase variants
GB0314210D0 (en)	2003-06-18	2003-07-23	Unilever Plc	Laundry treatment compositions
EP1678296B1 (en)	2003-10-23	2011-07-13	Novozymes A/S	Protease with improved stability in detergents
DE10353603B4 (de) *	2003-11-17	2006-01-19	Clariant Gmbh	Verwendung von Ethercarbonsäuren auf Basis alkoxylierter Mono-, Di- und/oder Tri(1-phenylethyl)phenole in Kühlschmiermitteln
DK1694847T3 (da)	2003-11-19	2012-09-03	Danisco Us Inc	Serinproteaser, nucleinsyrer kodende for serinenzymer og vektorer og værtsceller omfattende disse.
GB0420203D0 (en)	2004-09-11	2004-10-13	Unilever Plc	Laundry treatment compositions
DE602005015234D1 (de)	2004-09-23	2009-08-13	Unilever Nv	Zusammensetzungen zur wäschebehandlung
GB0421145D0 (en)	2004-09-23	2004-10-27	Unilever Plc	Laundry treatment compositions
DE102004052007B4 (de)	2004-10-25	2007-12-06	Müller Weingarten AG	Antriebssystem einer Umformpresse
ATE529505T1 (de)	2005-07-08	2011-11-15	Novozymes As	Subtilase varianten
ES2333994T3 (es)	2006-08-10	2010-03-03	Unilever N.V.	Composicion de oscurecimiento.
CN101583704B (zh)	2007-01-19	2013-05-15	宝洁公司	包含用于纤维质基底的增白剂的衣物洗涤护理组合物
WO2008141880A1 (en)	2007-05-18	2008-11-27	Unilever Plc	Triphenodioxazine dyes
DE102007038031A1 (de)	2007-08-10	2009-06-04	Henkel Ag & Co. Kgaa	Mittel enthaltend Proteasen
CN102015989B (zh)	2008-05-02	2012-07-04	荷兰联合利华有限公司	减少污斑的颗粒
BRPI0912867B1 (pt)	2008-05-20	2020-08-11	Unilever N.V	Composição de tratamento para lavagem e método caseiro para tratamento de têxteis
EP2403931B1 (en)	2009-03-05	2014-03-19	Unilever PLC	Dye radical initiators
CN102348769A (zh)	2009-03-12	2012-02-08	荷兰联合利华有限公司	染料-聚合物配方
WO2010148624A1 (en)	2009-06-26	2010-12-29	Unilever Plc	Dye polymers
CN104946427A (zh)	2009-09-25	2015-09-30	诺维信公司	蛋白酶变体的用途
CN102648273B (zh)	2009-09-25	2017-04-26	诺维信公司	枯草蛋白酶变体
WO2012054058A1 (en)	2010-10-22	2012-04-26	The Procter & Gamble Company	Bis-azo colorants for use as bluing agents
US20120101018A1 (en)	2010-10-22	2012-04-26	Gregory Scot Miracle	Bis-azo colorants for use as bluing agents
JP6129740B2 (ja)	2010-10-22	2017-05-17	ミリケン・アンド・カンパニーＭｉｌｌｉｋｅｎ＆Ｃｏｍｐａｎｙ	青味剤用ビス−アゾ着色剤
CA2817718C (en)	2010-11-12	2016-02-09	The Procter & Gamble Company	Laundry care compositions comprising charged thiophene azo dyes
RU2014111054A (ru) *	2011-08-31	2015-10-10	Акцо Нобель Кемикалз Интернэшнл Б.В.	Стиральные моющие композиции, содержащие грязеотталкивающее вещество
WO2013087286A1 (en)	2011-12-12	2013-06-20	Unilever Plc	Laundry compositions
JP6203812B2 (ja)	2012-03-19	2017-09-27	ミリケン・アンド・カンパニーＭｉｌｌｉｋｅｎ＆Ｃｏｍｐａｎｙ	カルボキシレート染料
WO2013151970A1 (en)	2012-04-03	2013-10-10	The Procter & Gamble Company	Laundry detergent composition comprising water-soluble phthalocyanine compound

2016
- 2016-04-26 BR BR112017025607-0A patent/BR112017025607B1/pt active IP Right Grant
- 2016-04-26 WO PCT/EP2016/059313 patent/WO2016192905A1/en active Search and Examination
- 2016-04-26 CN CN201680026582.8A patent/CN107835851B/zh active Active
- 2016-04-26 TR TR2019/06836T patent/TR201906836T4/tr unknown
- 2016-04-26 EP EP16718686.5A patent/EP3303536B1/en active Active
- 2016-06-01 AR ARP160101597A patent/AR104843A1/es active IP Right Grant

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

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BR112017025607B1 (pt)	2022-08-30
EP3303536A1 (en)	2018-04-11
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AR104843A1 (es)	2017-08-16
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