ES2247011T3 - Composiciones antimicrobianas que contienen compuestos de amonio cuaternario, silanos y otros desinfectantes con furanonas. - Google Patents
Composiciones antimicrobianas que contienen compuestos de amonio cuaternario, silanos y otros desinfectantes con furanonas.Info
- Publication number
- ES2247011T3 ES2247011T3 ES01273631T ES01273631T ES2247011T3 ES 2247011 T3 ES2247011 T3 ES 2247011T3 ES 01273631 T ES01273631 T ES 01273631T ES 01273631 T ES01273631 T ES 01273631T ES 2247011 T3 ES2247011 T3 ES 2247011T3
- Authority
- ES
- Spain
- Prior art keywords
- composition
- furanone
- moderate amount
- amount
- percent
- Prior art date
- 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.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 115
- 230000000845 anti-microbial effect Effects 0.000 title claims abstract description 49
- 239000000645 desinfectant Substances 0.000 title claims description 16
- 150000002241 furanones Chemical class 0.000 title description 43
- 150000003863 ammonium salts Chemical group 0.000 title 1
- 150000001282 organosilanes Chemical class 0.000 claims abstract description 57
- RHDGNLCLDBVESU-UHFFFAOYSA-N but-3-en-4-olide Chemical compound O=C1CC=CO1 RHDGNLCLDBVESU-UHFFFAOYSA-N 0.000 claims abstract description 55
- 230000002195 synergetic effect Effects 0.000 claims abstract description 25
- 150000003856 quaternary ammonium compounds Chemical class 0.000 claims description 32
- 150000001875 compounds Chemical class 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 15
- 239000004094 surface-active agent Substances 0.000 claims description 15
- 241000233866 Fungi Species 0.000 claims description 14
- -1 octyl decyl Chemical group 0.000 claims description 14
- 241000894006 Bacteria Species 0.000 claims description 13
- 238000004140 cleaning Methods 0.000 claims description 13
- 239000004599 antimicrobial Substances 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 241000191967 Staphylococcus aureus Species 0.000 claims description 9
- 150000003868 ammonium compounds Chemical class 0.000 claims description 9
- 244000005700 microbiome Species 0.000 claims description 8
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 8
- 229940123208 Biguanide Drugs 0.000 claims description 7
- RUPBZQFQVRMKDG-UHFFFAOYSA-M Didecyldimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCC[N+](C)(C)CCCCCCCCCC RUPBZQFQVRMKDG-UHFFFAOYSA-M 0.000 claims description 6
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims description 6
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- 241000223602 Alternaria alternata Species 0.000 claims description 5
- 241001149955 Cladosporium cladosporioides Species 0.000 claims description 5
- 150000001412 amines Chemical class 0.000 claims description 5
- 125000003844 furanonyl group Chemical group 0.000 claims description 5
- 241000223678 Aureobasidium pullulans Species 0.000 claims description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 4
- 241001507673 Penicillium digitatum Species 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 4
- 150000001720 carbohydrates Chemical class 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 229960004670 didecyldimethylammonium chloride Drugs 0.000 claims description 4
- XNCOSPRUTUOJCJ-UHFFFAOYSA-N Biguanide Chemical compound NC(N)=NC(N)=N XNCOSPRUTUOJCJ-UHFFFAOYSA-N 0.000 claims description 3
- 241000222122 Candida albicans Species 0.000 claims description 3
- 108010077895 Sarcosine Proteins 0.000 claims description 3
- 229940095731 candida albicans Drugs 0.000 claims description 3
- 125000002091 cationic group Chemical group 0.000 claims description 3
- WSFMFXQNYPNYGG-UHFFFAOYSA-M dimethyl-octadecyl-(3-trimethoxysilylpropyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCC[Si](OC)(OC)OC WSFMFXQNYPNYGG-UHFFFAOYSA-M 0.000 claims description 3
- 239000012530 fluid Substances 0.000 claims description 3
- 239000002736 nonionic surfactant Substances 0.000 claims description 3
- ROSDSFDQCJNGOL-UHFFFAOYSA-N protonated dimethyl amine Natural products CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims description 3
- 229940043230 sarcosine Drugs 0.000 claims description 3
- 229960000686 benzalkonium chloride Drugs 0.000 claims description 2
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 claims description 2
- 239000003205 fragrance Substances 0.000 claims description 2
- 239000004615 ingredient Substances 0.000 claims description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims 1
- JMHWNJGXUIJPKG-UHFFFAOYSA-N CC(=O)O[SiH](CC=C)OC(C)=O Chemical compound CC(=O)O[SiH](CC=C)OC(C)=O JMHWNJGXUIJPKG-UHFFFAOYSA-N 0.000 claims 1
- AXPYABZPAWSUMG-UHFFFAOYSA-M didecyl-methyl-(3-trimethoxysilylpropyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCC[N+](C)(CCC[Si](OC)(OC)OC)CCCCCCCCCC AXPYABZPAWSUMG-UHFFFAOYSA-M 0.000 claims 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 230000005764 inhibitory process Effects 0.000 description 21
- 241000894007 species Species 0.000 description 19
- 238000012360 testing method Methods 0.000 description 17
- 230000012010 growth Effects 0.000 description 16
- 238000009472 formulation Methods 0.000 description 14
- 239000000047 product Substances 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- 239000011521 glass Substances 0.000 description 8
- 239000012085 test solution Substances 0.000 description 8
- 241000228245 Aspergillus niger Species 0.000 description 6
- 229940027983 antiseptic and disinfectant quaternary ammonium compound Drugs 0.000 description 6
- 230000001580 bacterial effect Effects 0.000 description 6
- 238000004809 thin layer chromatography Methods 0.000 description 6
- 239000004480 active ingredient Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 230000002538 fungal effect Effects 0.000 description 5
- 230000002401 inhibitory effect Effects 0.000 description 5
- 229920001817 Agar Polymers 0.000 description 4
- 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 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- 239000008272 agar Substances 0.000 description 4
- 239000002738 chelating agent Substances 0.000 description 4
- 230000003247 decreasing effect Effects 0.000 description 4
- 238000011282 treatment Methods 0.000 description 4
- UKAUYVFTDYCKQA-UHFFFAOYSA-N -2-Amino-4-hydroxybutanoic acid Natural products OC(=O)C(N)CCO UKAUYVFTDYCKQA-UHFFFAOYSA-N 0.000 description 3
- 241000192125 Firmicutes Species 0.000 description 3
- UKAUYVFTDYCKQA-VKHMYHEASA-N L-homoserine Chemical compound OC(=O)[C@@H](N)CCO UKAUYVFTDYCKQA-VKHMYHEASA-N 0.000 description 3
- 230000006870 function Effects 0.000 description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 description 3
- 150000002596 lactones Chemical class 0.000 description 3
- 239000001965 potato dextrose agar Substances 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 210000002700 urine Anatomy 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- URDCARMUOSMFFI-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]ethyl-(2-hydroxyethyl)amino]acetic acid Chemical compound OCCN(CC(O)=O)CCN(CC(O)=O)CC(O)=O URDCARMUOSMFFI-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 241000195493 Cryptophyta Species 0.000 description 2
- 241001519550 Delisea Species 0.000 description 2
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 2
- 229920002257 Plurafac® Polymers 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 150000004283 biguanides Chemical class 0.000 description 2
- 239000003139 biocide Substances 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000008139 complexing agent Substances 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 230000009931 harmful effect Effects 0.000 description 2
- QJPWUUJVYOJNMH-UHFFFAOYSA-N homoserine lactone Chemical compound NC1CCOC1=O QJPWUUJVYOJNMH-UHFFFAOYSA-N 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229960003330 pentetic acid Drugs 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 230000011664 signaling Effects 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- WMDZKDKPYCNCDZ-UHFFFAOYSA-N 2-(2-butoxypropoxy)propan-1-ol Chemical compound CCCCOC(C)COC(C)CO WMDZKDKPYCNCDZ-UHFFFAOYSA-N 0.000 description 1
- GUUULVAMQJLDSY-UHFFFAOYSA-N 4,5-dihydro-1,2-thiazole Chemical class C1CC=NS1 GUUULVAMQJLDSY-UHFFFAOYSA-N 0.000 description 1
- 241000223600 Alternaria Species 0.000 description 1
- 241000228212 Aspergillus Species 0.000 description 1
- 241000223651 Aureobasidium Species 0.000 description 1
- 241001474374 Blennius Species 0.000 description 1
- 241000222120 Candida <Saccharomycetales> Species 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000222290 Cladosporium Species 0.000 description 1
- 241000122827 Delisea pulchra Species 0.000 description 1
- JGFDZZLUDWMUQH-UHFFFAOYSA-N Didecyldimethylammonium Chemical compound CCCCCCCCCC[N+](C)(C)CCCCCCCCCC JGFDZZLUDWMUQH-UHFFFAOYSA-N 0.000 description 1
- 241000588914 Enterobacter Species 0.000 description 1
- 241000588722 Escherichia Species 0.000 description 1
- 241000588724 Escherichia coli Species 0.000 description 1
- 206010020751 Hypersensitivity Diseases 0.000 description 1
- 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 1
- 241000122235 Junco hyemalis Species 0.000 description 1
- 241000588748 Klebsiella Species 0.000 description 1
- 241000588915 Klebsiella aerogenes Species 0.000 description 1
- 241000588747 Klebsiella pneumoniae Species 0.000 description 1
- QJPWUUJVYOJNMH-VKHMYHEASA-N L-homoserine lactone Chemical compound N[C@H]1CCOC1=O QJPWUUJVYOJNMH-VKHMYHEASA-N 0.000 description 1
- 108091077107 LuxS family Proteins 0.000 description 1
- 241000228143 Penicillium Species 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 241000588769 Proteus <enterobacteria> Species 0.000 description 1
- 241000588770 Proteus mirabilis Species 0.000 description 1
- 241000589516 Pseudomonas Species 0.000 description 1
- 241000589517 Pseudomonas aeruginosa Species 0.000 description 1
- 241000607142 Salmonella Species 0.000 description 1
- 241001354013 Salmonella enterica subsp. enterica serovar Enteritidis Species 0.000 description 1
- 241000607768 Shigella Species 0.000 description 1
- 241000607760 Shigella sonnei Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 241001279361 Stachybotrys Species 0.000 description 1
- 241001279364 Stachybotrys chartarum Species 0.000 description 1
- 241000191940 Staphylococcus Species 0.000 description 1
- 241000223238 Trichophyton Species 0.000 description 1
- 241000223229 Trichophyton rubrum Species 0.000 description 1
- NJMVHBQEIKOPIT-UHFFFAOYSA-N acetic acid 2-(2-aminoethylamino)ethanol Chemical compound CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O.NCCNCCO NJMVHBQEIKOPIT-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000006177 alkyl benzyl group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 208000006673 asthma Diseases 0.000 description 1
- 229960001716 benzalkonium Drugs 0.000 description 1
- CYDRXTMLKJDRQH-UHFFFAOYSA-N benzododecinium Chemical compound CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 CYDRXTMLKJDRQH-UHFFFAOYSA-N 0.000 description 1
- 229940073608 benzyl chloride Drugs 0.000 description 1
- 150000005524 benzylchlorides Chemical class 0.000 description 1
- 239000007767 bonding agent Substances 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- VIHAEDVKXSOUAT-UHFFFAOYSA-N but-2-en-4-olide Chemical class O=C1OCC=C1 VIHAEDVKXSOUAT-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 230000008568 cell cell communication Effects 0.000 description 1
- 230000010261 cell growth Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- CZIAHOKVOQSYHN-UHFFFAOYSA-N didecyl-methyl-(3-trimethoxysilylpropyl)azanium Chemical compound CCCCCCCCCC[N+](C)(CCC[Si](OC)(OC)OC)CCCCCCCCCC CZIAHOKVOQSYHN-UHFFFAOYSA-N 0.000 description 1
- 229940078672 didecyldimethylammonium Drugs 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229940092559 enterobacter aerogenes Drugs 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 150000002169 ethanolamines Chemical class 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229930182470 glycoside Natural products 0.000 description 1
- 150000002338 glycosides Chemical class 0.000 description 1
- 230000009036 growth inhibition Effects 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 230000005802 health problem Effects 0.000 description 1
- 235000003642 hunger Nutrition 0.000 description 1
- 150000001469 hydantoins Chemical class 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 229940035535 iodophors Drugs 0.000 description 1
- 238000003760 magnetic stirring Methods 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 238000000386 microscopy Methods 0.000 description 1
- 230000004001 molecular interaction Effects 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
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 244000039328 opportunistic pathogen Species 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 230000008447 perception Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 230000018612 quorum sensing Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 229940115939 shigella sonnei Drugs 0.000 description 1
- 230000019491 signal transduction Effects 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000001974 tryptic soy broth Substances 0.000 description 1
- 108010050327 trypticase-soy broth Proteins 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/08—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with oxygen as the ring hetero atom
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- General Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Detergent Compositions (AREA)
- Cleaning In General (AREA)
- Cleaning By Liquid Or Steam (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US986301 | 1992-12-07 | ||
| US24925300P | 2000-11-17 | 2000-11-17 | |
| US249253P | 2000-11-17 | ||
| US09/986,301 US6528472B2 (en) | 2000-11-17 | 2001-11-08 | Antimicrobial compositions containing quaternary ammonium compounds, silanes and other disinfectants with furanones |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2247011T3 true ES2247011T3 (es) | 2006-03-01 |
Family
ID=26939928
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES01273631T Expired - Lifetime ES2247011T3 (es) | 2000-11-17 | 2001-11-16 | Composiciones antimicrobianas que contienen compuestos de amonio cuaternario, silanos y otros desinfectantes con furanonas. |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US6528472B2 (enExample) |
| EP (1) | EP1349454B1 (enExample) |
| JP (1) | JP4223814B2 (enExample) |
| AR (1) | AR031478A1 (enExample) |
| AT (1) | ATE308243T1 (enExample) |
| CA (1) | CA2428789A1 (enExample) |
| DE (1) | DE60114665T2 (enExample) |
| ES (1) | ES2247011T3 (enExample) |
| MX (1) | MXPA03004359A (enExample) |
| TW (1) | TWI244394B (enExample) |
| WO (1) | WO2002080677A1 (enExample) |
Families Citing this family (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6716805B1 (en) * | 1999-09-27 | 2004-04-06 | The Procter & Gamble Company | Hard surface cleaning compositions, premoistened wipes, methods of use, and articles comprising said compositions or wipes and instructions for use resulting in easier cleaning and maintenance, improved surface appearance and/or hygiene under stress conditions such as no-rinse |
| US6814088B2 (en) * | 1999-09-27 | 2004-11-09 | The Procter & Gamble Company | Aqueous compositions for treating a surface |
| US20100160445A1 (en) * | 2002-01-17 | 2010-06-24 | Carlson Paul E | Synergistic Mixtures of OPP and DGH |
| US6928664B2 (en) * | 2002-10-24 | 2005-08-16 | Gary L. Price | Microbiostatic garment |
| US20050008676A1 (en) * | 2002-12-19 | 2005-01-13 | Yongxing Qiu | Medical devices having antimicrobial coatings thereon |
| US20050087216A1 (en) * | 2003-10-23 | 2005-04-28 | Dudjak Scott B. | Exterior surface cleaner and method of use |
| US8257780B2 (en) * | 2003-10-31 | 2012-09-04 | Resource Development L.L.C. | Therapeutic composition containing an organosilane quaternary compound and hydrogen peroxide for treating skin disorders and methods of using |
| US6994890B2 (en) * | 2003-10-31 | 2006-02-07 | Resource Development L.L.C. | Cleaning and multifunctional coating composition containing an organosilane quaternary compound and hydrogen peroxide |
| EP1706126A4 (en) * | 2003-12-04 | 2009-07-01 | Biofilms Strategies Inc | METHOD AND COMPOSITIONS FOR PREVENTING THE PREPARATION OF BIOFILMS, REDUCING EXISTING BIOFILMS, AND REDUCING EXISTING BIOFILMS AND REDUCING BACTERIA POPULATIONS |
| US8999363B2 (en) * | 2005-02-07 | 2015-04-07 | Sishield Technologies, Inc. | Methods and compositions for antimicrobial surfaces |
| US8999357B2 (en) * | 2005-02-07 | 2015-04-07 | Sishield Technologies, Inc. | Methods and compositions for biocidal treatments |
| DE102005020759A1 (de) * | 2005-05-02 | 2006-11-09 | Henkel Kgaa | Halomethylen-Alkanone und Furanone als Biofilmblocker |
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| US5411585A (en) | 1991-02-15 | 1995-05-02 | S. C. Johnson & Son, Inc. | Production of stable hydrolyzable organosilane solutions |
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| AUPP303498A0 (en) | 1998-04-17 | 1998-05-14 | Unisearch Limited | Inhibition of gram positive bacteria |
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| AUPQ475599A0 (en) | 1999-12-17 | 2000-01-20 | Unisearch Limited | Inhibition of two-component transduction systems |
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| AUPQ629000A0 (en) | 2000-03-16 | 2000-04-15 | Unisearch Limited | Inhibition of fungi |
| WO2001085664A2 (en) | 2000-05-10 | 2001-11-15 | Princeton University | Compounds and methods for regulating bacterial growth and pathogenesis |
-
2001
- 2001-11-08 US US09/986,301 patent/US6528472B2/en not_active Expired - Lifetime
- 2001-11-16 DE DE60114665T patent/DE60114665T2/de not_active Expired - Fee Related
- 2001-11-16 JP JP2002578725A patent/JP4223814B2/ja not_active Expired - Fee Related
- 2001-11-16 EP EP01273631A patent/EP1349454B1/en not_active Expired - Lifetime
- 2001-11-16 WO PCT/US2001/043886 patent/WO2002080677A1/en not_active Ceased
- 2001-11-16 ES ES01273631T patent/ES2247011T3/es not_active Expired - Lifetime
- 2001-11-16 MX MXPA03004359A patent/MXPA03004359A/es unknown
- 2001-11-16 AT AT01273631T patent/ATE308243T1/de not_active IP Right Cessation
- 2001-11-16 CA CA002428789A patent/CA2428789A1/en not_active Abandoned
- 2001-11-19 TW TW090128625A patent/TWI244394B/zh not_active IP Right Cessation
- 2001-11-19 AR ARP010105393A patent/AR031478A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US6528472B2 (en) | 2003-03-04 |
| TWI244394B (en) | 2005-12-01 |
| DE60114665T2 (de) | 2006-07-20 |
| JP2004524367A (ja) | 2004-08-12 |
| JP4223814B2 (ja) | 2009-02-12 |
| MXPA03004359A (es) | 2005-04-19 |
| CA2428789A1 (en) | 2002-10-17 |
| AR031478A1 (es) | 2003-09-24 |
| EP1349454A1 (en) | 2003-10-08 |
| EP1349454B1 (en) | 2005-11-02 |
| WO2002080677A1 (en) | 2002-10-17 |
| DE60114665D1 (de) | 2005-12-08 |
| ATE308243T1 (de) | 2005-11-15 |
| US20020111282A1 (en) | 2002-08-15 |
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