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 |
|---|---|---|---|---|
| US7169744B2 (en) | 2002-06-06 | 2007-01-30 | Procter & Gamble Company | Organic catalyst with enhanced solubility |
| US7557076B2 (en) | 2002-06-06 | 2009-07-07 | The Procter & Gamble Company | Organic catalyst with enhanced enzyme compatibility |
| 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 |
| PL1754781T3 (pl) * | 2005-08-19 | 2013-09-30 | Procter & Gamble | Stała kompozycja detergentowa do prania zawierająca anionowy środek powierzchniowo czynny i technologię wspomagania wapniem |
| 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 |
| DE602006013778D1 (de) | 2006-01-23 | 2010-06-02 | Procter & Gamble | Zusammensetzung enthaltend vorgeformte Persäure und einen Bleichmittelkatalysator |
| AR059153A1 (es) | 2006-01-23 | 2008-03-12 | Procter & Gamble | Una composicion que comprende una lipasa y un catalizador de blanqueador |
| WO2008007319A2 (en) | 2006-07-07 | 2008-01-17 | The Procter & Gamble Company | A composition comprising a cellulase and a bleach catalyst |
| CN102459249A (zh) | 2009-05-22 | 2012-05-16 | 埃克塞里艾克西斯公司 | 作为PI3K/mTOR抑制剂的苯并氧氮杂环庚三烯以及它们使用与制造方法 |
| JP2012528165A (ja) | 2009-05-26 | 2012-11-12 | エクセリクシス， インク． | ＰＩ３Ｋ／ｍＴＯＲの阻害剤としてのベンゾキサゼピンならびにそれらの使用および製造方法 |
| AU2010276537B2 (en) | 2009-07-27 | 2015-04-16 | Gilead Sciences, Inc. | Fused heterocyclic compounds as ion channel modulators |
| US20110240510A1 (en) * | 2010-04-06 | 2011-10-06 | Johan Maurice Theo De Poortere | Optimized release of bleaching systems in laundry detergents |
| MX2012015096A (es) | 2010-07-02 | 2013-05-28 | Gilead Sciences Inc | Compuestos heterociclicos fusionados como moduladores del canal ion. |
| EP2707361B1 (de) | 2011-05-10 | 2017-08-23 | Gilead Sciences, Inc. | Kondensierte heterozyklische verbindungen als natriumkanalmodulatoren |
| NO3175985T3 (de) | 2011-07-01 | 2018-04-28 | ||
| TWI622583B (zh) | 2011-07-01 | 2018-05-01 | 基利科學股份有限公司 | 作為離子通道調節劑之稠合雜環化合物 |
| BR112014029752A2 (pt) * | 2012-05-30 | 2017-06-27 | Clariant Finance Bvi Ltd | uso de n-metil-n-acilglucaminas como estabilizadores de frio em soluções de tensoativos |
| 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 |
| US5370826A (en) * | 1993-11-12 | 1994-12-06 | Lever Brothers Company, Division Of Conopco, Inc. | Quaternay oxaziridinium salts as bleaching compounds |
| WO1995013352A1 (en) * | 1993-11-12 | 1995-05-18 | Unilever N.V. | Imine quaternary salts as bleach catalysts |
| EP0728183B1 (de) * | 1993-11-12 | 1998-03-25 | Unilever N.V. | Aktivierung von bleichmittel vorläufern mittels quaternärer iminiumsalze |
| 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 AU AU70721/00A patent/AU7072100A/en not_active Abandoned
- 2000-08-25 TR TR2002/00471T patent/TR200200471T2/xx unknown
- 2000-08-25 JP JP2001520822A patent/JP2003508585A/ja not_active Withdrawn
- 2000-08-25 AT AT00959387T patent/ATE311432T1/de not_active IP Right Cessation
- 2000-08-25 CN CN00814999.2A patent/CN1384868A/zh active Pending
- 2000-08-25 CZ CZ2002722A patent/CZ2002722A3/cs unknown
- 2000-08-25 MX MXPA02002128A patent/MXPA02002128A/es active IP Right Grant
- 2000-08-25 WO PCT/US2000/023317 patent/WO2001016274A1/en active IP Right Grant
- 2000-08-25 EP EP00959387A patent/EP1206519B1/de not_active Expired - Lifetime
- 2000-08-25 BR BR0014151-8A patent/BR0014151A/pt not_active Application Discontinuation
- 2000-08-25 DE DE60024463T patent/DE60024463T2/de not_active Expired - Lifetime
- 2000-08-25 CA CA002382023A patent/CA2382023A1/en not_active Abandoned
- 2000-08-25 ES ES00959387T patent/ES2252054T3/es not_active Expired - Lifetime
- 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 |
|---|---|
| ES2252054T3 (es) | 2006-05-16 |
| MA25602A1 (fr) | 2002-12-31 |
| ATE311432T1 (de) | 2005-12-15 |
| AR027846A1 (es) | 2003-04-16 |
| BR0014151A (pt) | 2002-05-07 |
| DE60024463D1 (de) | 2006-01-05 |
| WO2001016274A9 (en) | 2007-06-14 |
| WO2001016274A1 (en) | 2001-03-08 |
| CA2382023A1 (en) | 2001-03-08 |
| TR200200471T2 (tr) | 2002-05-21 |
| EP1206519A1 (de) | 2002-05-22 |
| AU7072100A (en) | 2001-03-26 |
| DE60024463T2 (de) | 2006-08-17 |
| CN1384868A (zh) | 2002-12-11 |
| EP1206519B1 (de) | 2005-11-30 |
| CZ2002722A3 (cs) | 2002-10-16 |
| EG22867A (en) | 2003-09-30 |
| JP2003508585A (ja) | 2003-03-04 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant or registration |