MXPA02002128A - Componentes para formulacion estable, composiciones y metodos para lavanderia que los emplean. - Google Patents
Componentes para formulacion estable, composiciones y metodos para lavanderia que los emplean.Info
- Publication number
- MXPA02002128A MXPA02002128A MXPA02002128A MXPA02002128A MXPA02002128A MX PA02002128 A MXPA02002128 A MX PA02002128A MX PA02002128 A MXPA02002128 A MX PA02002128A MX PA02002128 A MXPA02002128 A MX PA02002128A MX PA02002128 A MXPA02002128 A MX PA02002128A
- Authority
- MX
- Mexico
- Prior art keywords
- group
- substituted
- alkyl
- heterocyclic ring
- aryl
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 361
- 238000000034 method Methods 0.000 title claims abstract description 55
- 238000009472 formulation Methods 0.000 title abstract description 30
- 239000003054 catalyst Substances 0.000 claims abstract description 211
- 150000001875 compounds Chemical class 0.000 claims abstract description 164
- 238000004061 bleaching Methods 0.000 claims abstract description 156
- 239000007844 bleaching agent Substances 0.000 claims abstract description 85
- 150000001412 amines Chemical class 0.000 claims abstract description 42
- SJGALSBBFTYSBA-UHFFFAOYSA-N oxaziridine Chemical group C1NO1 SJGALSBBFTYSBA-UHFFFAOYSA-N 0.000 claims abstract description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 185
- -1 oxaziridinium cations Chemical class 0.000 claims description 162
- 125000003118 aryl group Chemical group 0.000 claims description 150
- 125000000623 heterocyclic group Chemical group 0.000 claims description 149
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 114
- 229910052739 hydrogen Inorganic materials 0.000 claims description 102
- 125000003545 alkoxy group Chemical group 0.000 claims description 92
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 91
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 85
- 102000004190 Enzymes Human genes 0.000 claims description 70
- 108090000790 Enzymes Proteins 0.000 claims description 70
- 239000003599 detergent Substances 0.000 claims description 62
- 239000004744 fabric Substances 0.000 claims description 62
- 229930194542 Keto Natural products 0.000 claims description 58
- 125000000468 ketone group Chemical group 0.000 claims description 58
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 58
- BZWKPZBXAMTXNQ-UHFFFAOYSA-N sulfurocyanidic acid Chemical compound OS(=O)(=O)C#N BZWKPZBXAMTXNQ-UHFFFAOYSA-N 0.000 claims description 57
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 56
- 239000004094 surface-active agent Substances 0.000 claims description 55
- 239000003795 chemical substances by application Substances 0.000 claims description 52
- 239000002253 acid Substances 0.000 claims description 50
- 238000005406 washing Methods 0.000 claims description 49
- 229910001868 water Inorganic materials 0.000 claims description 49
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 48
- 150000003839 salts Chemical class 0.000 claims description 45
- 239000012190 activator Substances 0.000 claims description 42
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims description 40
- 229920006395 saturated elastomer Polymers 0.000 claims description 40
- 125000001424 substituent group Chemical group 0.000 claims description 35
- 229910052760 oxygen Inorganic materials 0.000 claims description 31
- 239000001301 oxygen Substances 0.000 claims description 30
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 28
- 150000007513 acids Chemical class 0.000 claims description 27
- 125000005129 aryl carbonyl group Chemical group 0.000 claims description 24
- 125000004181 carboxyalkyl group Chemical group 0.000 claims description 24
- 125000003368 amide group Chemical group 0.000 claims description 21
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 21
- 125000002947 alkylene group Chemical group 0.000 claims description 19
- 150000001768 cations Chemical class 0.000 claims description 19
- 239000000654 additive Substances 0.000 claims description 17
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 17
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical class [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 claims description 17
- 230000000996 additive effect Effects 0.000 claims description 15
- 229920000831 ionic polymer Polymers 0.000 claims description 15
- 125000002091 cationic group Chemical group 0.000 claims description 13
- 239000002270 dispersing agent Substances 0.000 claims description 13
- 230000002255 enzymatic effect Effects 0.000 claims description 13
- 238000012546 transfer Methods 0.000 claims description 13
- 125000000129 anionic group Chemical group 0.000 claims description 10
- 239000002738 chelating agent Substances 0.000 claims description 10
- FAGGUIDTQQXDSJ-UHFFFAOYSA-N 3-benzoylazepan-2-one Chemical compound C=1C=CC=CC=1C(=O)C1CCCCNC1=O FAGGUIDTQQXDSJ-UHFFFAOYSA-N 0.000 claims description 8
- 230000002401 inhibitory effect Effects 0.000 claims description 8
- FRPJTGXMTIIFIT-UHFFFAOYSA-N tetraacetylethylenediamine Chemical compound CC(=O)C(N)(C(C)=O)C(N)(C(C)=O)C(C)=O FRPJTGXMTIIFIT-UHFFFAOYSA-N 0.000 claims description 8
- 150000001408 amides Chemical class 0.000 claims description 7
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
- 239000002689 soil Substances 0.000 claims description 7
- GGAVUMZUOHJGGM-UHFFFAOYSA-N 2-decanoyloxybenzenesulfonic acid Chemical compound CCCCCCCCCC(=O)OC1=CC=CC=C1S(O)(=O)=O GGAVUMZUOHJGGM-UHFFFAOYSA-N 0.000 claims description 6
- 239000004927 clay Substances 0.000 claims description 6
- 150000002148 esters Chemical class 0.000 claims description 6
- FCJSHPDYVMKCHI-UHFFFAOYSA-N phenyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OC1=CC=CC=C1 FCJSHPDYVMKCHI-UHFFFAOYSA-N 0.000 claims description 6
- 239000003381 stabilizer Substances 0.000 claims description 6
- 239000003981 vehicle Substances 0.000 claims description 6
- 125000002837 carbocyclic group Chemical group 0.000 claims description 5
- 239000003086 colorant Substances 0.000 claims description 5
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 238000005187 foaming Methods 0.000 claims description 5
- 239000002304 perfume Substances 0.000 claims description 5
- 159000000000 sodium salts Chemical class 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 5
- CDWQJRGVYJQAIT-UHFFFAOYSA-N 3-benzoylpiperidin-2-one Chemical compound C=1C=CC=CC=1C(=O)C1CCCNC1=O CDWQJRGVYJQAIT-UHFFFAOYSA-N 0.000 claims description 4
- 125000005342 perphosphate group Chemical group 0.000 claims description 4
- KYVZSRPVPDAAKQ-UHFFFAOYSA-N 2-benzoyloxybenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1OC(=O)C1=CC=CC=C1 KYVZSRPVPDAAKQ-UHFFFAOYSA-N 0.000 claims description 3
- ZDKYIHHSXJTDKX-UHFFFAOYSA-N 2-dodecanoyloxybenzenesulfonic acid Chemical compound CCCCCCCCCCCC(=O)OC1=CC=CC=C1S(O)(=O)=O ZDKYIHHSXJTDKX-UHFFFAOYSA-N 0.000 claims description 3
- FNPBLXRYUROGSR-UHFFFAOYSA-N 2-undec-10-enoyloxybenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1OC(=O)CCCCCCCCC=C FNPBLXRYUROGSR-UHFFFAOYSA-N 0.000 claims description 3
- MQWCVVYEJGQDEL-UHFFFAOYSA-N 3-(4-nitrobenzoyl)azepan-2-one Chemical compound C1=CC([N+](=O)[O-])=CC=C1C(=O)C1C(=O)NCCCC1 MQWCVVYEJGQDEL-UHFFFAOYSA-N 0.000 claims description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 3
- JNIYAMTYWPMEGP-UHFFFAOYSA-N ClC1=CC=CC(C(=O)C2C(NCCCC2)=O)=C1 Chemical compound ClC1=CC=CC(C(=O)C2C(NCCCC2)=O)=C1 JNIYAMTYWPMEGP-UHFFFAOYSA-N 0.000 claims description 3
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 3
- AKDRUQMXFTYGSY-UHFFFAOYSA-N 4-[6-(nonanoylamino)hexanoyloxy]benzenesulfonic acid Chemical compound CCCCCCCCC(=O)NCCCCCC(=O)OC1=CC=C(S(O)(=O)=O)C=C1 AKDRUQMXFTYGSY-UHFFFAOYSA-N 0.000 claims description 2
- 239000000872 buffer Substances 0.000 claims description 2
- 239000002979 fabric softener Substances 0.000 claims description 2
- 125000001475 halogen functional group Chemical group 0.000 claims 34
- GLGNXYJARSMNGJ-VKTIVEEGSA-N (1s,2s,3r,4r)-3-[[5-chloro-2-[(1-ethyl-6-methoxy-2-oxo-4,5-dihydro-3h-1-benzazepin-7-yl)amino]pyrimidin-4-yl]amino]bicyclo[2.2.1]hept-5-ene-2-carboxamide Chemical compound CCN1C(=O)CCCC2=C(OC)C(NC=3N=C(C(=CN=3)Cl)N[C@H]3[C@H]([C@@]4([H])C[C@@]3(C=C4)[H])C(N)=O)=CC=C21 GLGNXYJARSMNGJ-VKTIVEEGSA-N 0.000 claims 1
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims 1
- 239000012459 cleaning agent Substances 0.000 claims 1
- 229940125758 compound 15 Drugs 0.000 claims 1
- 239000003623 enhancer Substances 0.000 claims 1
- 230000001965 increasing effect Effects 0.000 abstract description 15
- 150000002466 imines Chemical group 0.000 abstract description 3
- 150000003254 radicals Chemical class 0.000 description 80
- 229940088598 enzyme Drugs 0.000 description 69
- 238000004140 cleaning Methods 0.000 description 68
- 239000000243 solution Substances 0.000 description 66
- 239000000463 material Substances 0.000 description 49
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- 102000035195 Peptidases Human genes 0.000 description 37
- 239000004365 Protease Substances 0.000 description 34
- 239000000047 product Substances 0.000 description 33
- 239000007788 liquid Substances 0.000 description 32
- 239000000975 dye Substances 0.000 description 24
- 125000005843 halogen group Chemical group 0.000 description 24
- 108010084185 Cellulases Proteins 0.000 description 22
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- 102000004882 Lipase Human genes 0.000 description 20
- 239000004367 Lipase Substances 0.000 description 19
- 235000019421 lipase Nutrition 0.000 description 19
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 18
- 241000228215 Aspergillus aculeatus Species 0.000 description 18
- 238000002360 preparation method Methods 0.000 description 18
- 102000013142 Amylases Human genes 0.000 description 17
- 108010065511 Amylases Proteins 0.000 description 17
- 235000019418 amylase Nutrition 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
- 239000002736 nonionic surfactant Substances 0.000 description 17
- 150000004965 peroxy acids Chemical class 0.000 description 17
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- 238000000354 decomposition reaction Methods 0.000 description 16
- 241000894007 species Species 0.000 description 16
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- 239000011572 manganese Substances 0.000 description 15
- 230000000694 effects Effects 0.000 description 14
- 238000006467 substitution reaction Methods 0.000 description 14
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 13
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 13
- 229940025131 amylases Drugs 0.000 description 13
- 230000015572 biosynthetic process Effects 0.000 description 13
- 229910052751 metal Inorganic materials 0.000 description 13
- 239000002184 metal Substances 0.000 description 13
- 238000012360 testing method Methods 0.000 description 13
- 229910000323 aluminium silicate Inorganic materials 0.000 description 12
- 125000004432 carbon atom Chemical group C* 0.000 description 12
- 239000007859 condensation product Substances 0.000 description 12
- 239000006260 foam Substances 0.000 description 12
- 239000000758 substrate Substances 0.000 description 12
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 10
- 229910000272 alkali metal oxide Inorganic materials 0.000 description 10
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- 238000002835 absorbance Methods 0.000 description 9
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- 239000002585 base Substances 0.000 description 9
- 229910052799 carbon Inorganic materials 0.000 description 9
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- 239000008367 deionised water Substances 0.000 description 9
- 229910021641 deionized water Inorganic materials 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- 229910052723 transition metal Inorganic materials 0.000 description 9
- 239000010457 zeolite Substances 0.000 description 9
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 8
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical class [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 8
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- 150000002678 macrocyclic compounds Chemical class 0.000 description 8
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- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 7
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- 229910017052 cobalt Inorganic materials 0.000 description 7
- 239000010941 cobalt Substances 0.000 description 7
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- 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 6
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 6
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- 229910019142 PO4 Inorganic materials 0.000 description 6
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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 6
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- 235000015927 pasta Nutrition 0.000 description 1
- 239000000137 peptide hydrolase inhibitor Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 150000004968 peroxymonosulfuric acids Chemical class 0.000 description 1
- FHHJDRFHHWUPDG-UHFFFAOYSA-N peroxysulfuric acid Chemical compound OOS(O)(=O)=O FHHJDRFHHWUPDG-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
- PTMHPRAIXMAOOB-UHFFFAOYSA-N phosphoramidic acid Chemical class NP(O)(O)=O PTMHPRAIXMAOOB-UHFFFAOYSA-N 0.000 description 1
- 235000002949 phytic acid Nutrition 0.000 description 1
- 229940068041 phytic acid Drugs 0.000 description 1
- 239000000467 phytic acid Substances 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 229920000075 poly(4-vinylpyridine) Polymers 0.000 description 1
- 229920002006 poly(N-vinylimidazole) polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 238000006268 reductive amination reaction Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000002390 rotary evaporation Methods 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- BIXNGBXQRRXPLM-UHFFFAOYSA-K ruthenium(3+);trichloride;hydrate Chemical compound O.Cl[Ru](Cl)Cl BIXNGBXQRRXPLM-UHFFFAOYSA-K 0.000 description 1
- 238000011012 sanitization Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- COEZWFYORILMOM-UHFFFAOYSA-M sodium 4-[(2,4-dihydroxyphenyl)diazenyl]benzenesulfonate Chemical compound [Na+].OC1=CC(O)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 COEZWFYORILMOM-UHFFFAOYSA-M 0.000 description 1
- 235000012217 sodium aluminium silicate Nutrition 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 229910001948 sodium oxide Inorganic materials 0.000 description 1
- PFUVRDFDKPNGAV-UHFFFAOYSA-N sodium peroxide Chemical compound [Na+].[Na+].[O-][O-] PFUVRDFDKPNGAV-UHFFFAOYSA-N 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical group [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 125000005156 substituted alkylene group Chemical group 0.000 description 1
- 125000005650 substituted phenylene group Chemical group 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000000271 synthetic detergent Substances 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- MSLRPWGRFCKNIZ-UHFFFAOYSA-J tetrasodium;hydrogen peroxide;dicarbonate Chemical compound [Na+].[Na+].[Na+].[Na+].OO.OO.OO.[O-]C([O-])=O.[O-]C([O-])=O MSLRPWGRFCKNIZ-UHFFFAOYSA-J 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 125000000341 threoninyl group Chemical group [H]OC([H])(C([H])([H])[H])C([H])(N([H])[H])C(*)=O 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000000606 toothpaste Substances 0.000 description 1
- 229940034610 toothpaste Drugs 0.000 description 1
- GTZCVFVGUGFEME-UHFFFAOYSA-N trans-aconitic acid Natural products OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 description 1
- 229910001428 transition metal ion Inorganic materials 0.000 description 1
- 125000005208 trialkylammonium group Chemical group 0.000 description 1
- OHOTVSOGTVKXEL-UHFFFAOYSA-K trisodium;2-[bis(carboxylatomethyl)amino]propanoate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C(C)N(CC([O-])=O)CC([O-])=O OHOTVSOGTVKXEL-UHFFFAOYSA-K 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 239000004474 valine Substances 0.000 description 1
- 125000002987 valine group Chemical group [H]N([H])C([H])(C(*)=O)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 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
- C11D3/39—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
- C11D3/3917—Nitrogen-containing 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
- C11D3/3907—Organic compounds
- C11D3/3917—Nitrogen-containing compounds
- C11D3/392—Heterocyclic compounds, e.g. cyclic imides or lactames
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15117699P | 1999-08-27 | 1999-08-27 | |
| PCT/US2000/023317 WO2001016274A1 (en) | 1999-08-27 | 2000-08-25 | Stable formulation components, compositions and laundry methods employing same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA02002128A true MXPA02002128A (es) | 2002-09-02 |
Family
ID=22537634
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA02002128A MXPA02002128A (es) | 1999-08-27 | 2000-08-25 | Componentes para formulacion estable, composiciones y metodos para lavanderia que los emplean. |
Country Status (16)
| Country | Link |
|---|---|
| EP (1) | EP1206519B1 (de) |
| JP (1) | JP2003508585A (de) |
| CN (1) | CN1384868A (de) |
| AR (1) | AR027846A1 (de) |
| AT (1) | ATE311432T1 (de) |
| AU (1) | AU7072100A (de) |
| BR (1) | BR0014151A (de) |
| CA (1) | CA2382023A1 (de) |
| CZ (1) | CZ2002722A3 (de) |
| DE (1) | DE60024463T2 (de) |
| EG (1) | EG22867A (de) |
| ES (1) | ES2252054T3 (de) |
| MA (1) | MA25602A1 (de) |
| MX (1) | MXPA02002128A (de) |
| TR (1) | TR200200471T2 (de) |
| WO (1) | WO2001016274A1 (de) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7557076B2 (en) | 2002-06-06 | 2009-07-07 | The Procter & Gamble Company | Organic catalyst with enhanced enzyme compatibility |
| US7169744B2 (en) | 2002-06-06 | 2007-01-30 | Procter & Gamble Company | Organic catalyst with enhanced solubility |
| AR051659A1 (es) | 2005-06-17 | 2007-01-31 | Procter & Gamble | Una composicion que comprende un catalizador organico con compatibilidada enzimatica mejorada |
| EP1896561A2 (de) | 2005-06-17 | 2008-03-12 | Basf Se | Verfahren zur herstellung von bleichaktivatoren |
| ES2415872T3 (es) * | 2005-08-19 | 2013-07-29 | The Procter & Gamble Company | Composición detergente para lavado de ropa, sólida que comprende un tensioactivo detersivo aniónico y una tecnología de potenciación del calcio |
| US20070123440A1 (en) * | 2005-11-28 | 2007-05-31 | Loughnane Brian J | Stable odorant systems |
| CN101370921B (zh) | 2006-01-23 | 2014-08-13 | 宝洁公司 | 包含脂肪酶和漂白催化剂的组合物 |
| EP1811014B1 (de) | 2006-01-23 | 2010-04-21 | The Procter and Gamble Company | Zusammensetzung enthaltend vorgeformte Persäure und einen Bleichmittelkatalysator |
| WO2007087258A2 (en) | 2006-01-23 | 2007-08-02 | The Procter & Gamble Company | A composition comprising a lipase and a bleach catalyst |
| PH12009500020A1 (en) | 2006-07-07 | 2008-01-17 | Procter & Gamble | A composition comprising a cellulose and a bleach catalyst |
| KR20120034666A (ko) | 2009-05-22 | 2012-04-12 | 엑셀리시스, 인코포레이티드 | 증식성 질환에 대한 벤족사제핀 기반 ｐ１３ｋ／ｍｔ０ｒ의 억제제 |
| AU2010254200A1 (en) | 2009-05-26 | 2011-12-08 | Exelixis, Inc. | Benzoxazepines as inhibitors of PI3K/m TOR and methods of their use and manufacture |
| DK2464645T3 (en) | 2009-07-27 | 2017-10-23 | Gilead Sciences Inc | CONDENSED, HETEROCYCLIC COMPOUNDS AS IRON CHANNEL MODULATORS |
| US20110240510A1 (en) * | 2010-04-06 | 2011-10-06 | Johan Maurice Theo De Poortere | Optimized release of bleaching systems in laundry detergents |
| CN103096977B (zh) | 2010-07-02 | 2017-02-15 | 吉利德科学公司 | 作为离子通道调节剂的稠杂环化合物 |
| WO2012154760A1 (en) | 2011-05-10 | 2012-11-15 | Gilead Sciences, Inc. | Fused heterocyclic compounds as sodium channel modulators |
| TWI549944B (zh) | 2011-07-01 | 2016-09-21 | 吉李德科學股份有限公司 | 作為離子通道調節劑之稠合雜環化合物 |
| NO3175985T3 (de) | 2011-07-01 | 2018-04-28 | ||
| CN104394936B (zh) * | 2012-05-30 | 2017-08-25 | 科莱恩金融(Bvi)有限公司 | N‑甲基‑n‑酰基葡糖胺作为表面活性剂溶液中的低温稳定剂的用途 |
| JP6188199B2 (ja) * | 2013-05-20 | 2017-08-30 | ライオン株式会社 | 食器洗い機用洗浄剤 |
| WO2017182295A1 (en) * | 2016-04-18 | 2017-10-26 | Basf Se | Liquid cleaning compositions |
| EP3249034B1 (de) * | 2016-05-26 | 2019-03-20 | The Procter and Gamble Company | Wasserlöslicher einheitsdosisartikel mit einer pulverzusammensetzung |
| DE102016015660A1 (de) * | 2016-12-31 | 2018-07-05 | Weylchem Wiesbaden Gmbh | Granulate, deren Verwendung und Wasch- und Reinigungsmittel enthaltend diese |
| WO2024068248A1 (en) * | 2022-09-29 | 2024-04-04 | Unilever Ip Holdings B.V. | A solid cleaning and disinfection composition |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4194987A (en) * | 1978-12-26 | 1980-03-25 | Fmc Corporation | Peroxygen bleaching and compositions therefor |
| CA2176227C (en) * | 1993-11-12 | 2006-08-15 | Stephen Alan Madison | Imine quaternary salts as bleach catalysts |
| AU8106694A (en) * | 1993-11-12 | 1995-05-29 | Unilever Plc | Activation of bleach precursors with imine quaternary salts |
| US5370826A (en) * | 1993-11-12 | 1994-12-06 | Lever Brothers Company, Division Of Conopco, Inc. | Quaternay oxaziridinium salts as bleaching compounds |
| US5576282A (en) * | 1995-09-11 | 1996-11-19 | The Procter & Gamble Company | Color-safe bleach boosters, compositions and laundry methods employing same |
| US5817614A (en) * | 1996-08-29 | 1998-10-06 | Procter & Gamble Company | Color-safe bleach boosters, compositions and laundry methods employing same |
| DE19746290A1 (de) * | 1997-10-20 | 1999-04-22 | Clariant Gmbh | Verwendung von Aminonitril-N-oxiden als Bleichaktivatoren |
-
2000
- 2000-08-25 JP JP2001520822A patent/JP2003508585A/ja not_active Withdrawn
- 2000-08-25 CA CA002382023A patent/CA2382023A1/en not_active Abandoned
- 2000-08-25 EP EP00959387A patent/EP1206519B1/de not_active Expired - Lifetime
- 2000-08-25 DE DE60024463T patent/DE60024463T2/de not_active Expired - Lifetime
- 2000-08-25 AU AU70721/00A patent/AU7072100A/en not_active Abandoned
- 2000-08-25 AT AT00959387T patent/ATE311432T1/de not_active IP Right Cessation
- 2000-08-25 BR BR0014151-8A patent/BR0014151A/pt not_active Application Discontinuation
- 2000-08-25 TR TR2002/00471T patent/TR200200471T2/xx unknown
- 2000-08-25 CN CN00814999.2A patent/CN1384868A/zh active Pending
- 2000-08-25 MX MXPA02002128A patent/MXPA02002128A/es active IP Right Grant
- 2000-08-25 CZ CZ2002722A patent/CZ2002722A3/cs unknown
- 2000-08-25 ES ES00959387T patent/ES2252054T3/es not_active Expired - Lifetime
- 2000-08-25 WO PCT/US2000/023317 patent/WO2001016274A1/en active IP Right Grant
- 2000-08-27 EG EG20001108A patent/EG22867A/xx active
- 2000-08-28 AR ARP000104455A patent/AR027846A1/es active IP Right Grant
-
2002
- 2002-02-27 MA MA26531A patent/MA25602A1/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| WO2001016274A1 (en) | 2001-03-08 |
| DE60024463T2 (de) | 2006-08-17 |
| EP1206519B1 (de) | 2005-11-30 |
| DE60024463D1 (de) | 2006-01-05 |
| CN1384868A (zh) | 2002-12-11 |
| AR027846A1 (es) | 2003-04-16 |
| EG22867A (en) | 2003-09-30 |
| ES2252054T3 (es) | 2006-05-16 |
| WO2001016274A9 (en) | 2007-06-14 |
| ATE311432T1 (de) | 2005-12-15 |
| TR200200471T2 (tr) | 2002-05-21 |
| MA25602A1 (fr) | 2002-12-31 |
| EP1206519A1 (de) | 2002-05-22 |
| JP2003508585A (ja) | 2003-03-04 |
| CZ2002722A3 (cs) | 2002-10-16 |
| CA2382023A1 (en) | 2001-03-08 |
| AU7072100A (en) | 2001-03-26 |
| BR0014151A (pt) | 2002-05-07 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant or registration |