CN102308811B - 杀微生物剂组合物 - Google Patents
杀微生物剂组合物 Download PDFInfo
- Publication number
- CN102308811B CN102308811B CN201110230502.XA CN201110230502A CN102308811B CN 102308811 B CN102308811 B CN 102308811B CN 201110230502 A CN201110230502 A CN 201110230502A CN 102308811 B CN102308811 B CN 102308811B
- Authority
- CN
- China
- Prior art keywords
- ketone
- benzisothiazole
- microbicide
- isophthalic acid
- methyl isophthalic
- 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 - Fee Related
Links
- 230000003641 microbiacidal effect Effects 0.000 title claims abstract description 36
- 239000000203 mixture Substances 0.000 title claims abstract description 32
- 229940124561 microbicide Drugs 0.000 claims description 33
- 239000002855 microbicide agent Substances 0.000 claims description 29
- QQVIHTHCMHWDBS-UHFFFAOYSA-N perisophthalic acid Natural products OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 29
- 238000005660 chlorination reaction Methods 0.000 claims description 10
- WZZSEYALJBOYTI-UHFFFAOYSA-N [Cu+2].C(C)NCCO Chemical compound [Cu+2].C(C)NCCO WZZSEYALJBOYTI-UHFFFAOYSA-N 0.000 claims description 7
- JGFDZZLUDWMUQH-UHFFFAOYSA-N Didecyldimethylammonium Chemical compound CCCCCCCCCC[N+](C)(C)CCCCCCCCCC JGFDZZLUDWMUQH-UHFFFAOYSA-N 0.000 claims description 6
- 229940078672 didecyldimethylammonium Drugs 0.000 claims description 6
- 230000002195 synergetic effect Effects 0.000 abstract description 3
- RDWXSJCICPOOKO-UHFFFAOYSA-N 2-methyl-1,2-benzothiazol-3-one Chemical compound C1=CC=C2C(=O)N(C)SC2=C1 RDWXSJCICPOOKO-UHFFFAOYSA-N 0.000 abstract 1
- 244000005700 microbiome Species 0.000 description 18
- -1 mono laurate propylene glycol ester Chemical class 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- ARIWANIATODDMH-UHFFFAOYSA-N rac-1-monolauroylglycerol Chemical compound CCCCCCCCCCCC(=O)OCC(O)CO ARIWANIATODDMH-UHFFFAOYSA-N 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- 230000000845 anti-microbial effect Effects 0.000 description 9
- MVTVVKOMNZGDGD-UHFFFAOYSA-M didecyl(dimethyl)azanium;hydron;carbonate Chemical compound OC([O-])=O.CCCCCCCCCC[N+](C)(C)CCCCCCCCCC MVTVVKOMNZGDGD-UHFFFAOYSA-M 0.000 description 8
- 230000012010 growth Effects 0.000 description 8
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 8
- 239000000839 emulsion Substances 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 239000004530 micro-emulsion Substances 0.000 description 7
- 239000004094 surface-active agent Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 239000012141 concentrate Substances 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- GNMLQBQMKSVYDW-UHFFFAOYSA-N [Cu].C(C)NCCO Chemical compound [Cu].C(C)NCCO GNMLQBQMKSVYDW-UHFFFAOYSA-N 0.000 description 5
- 239000000853 adhesive Substances 0.000 description 5
- 230000001070 adhesive effect Effects 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000006185 dispersion Substances 0.000 description 5
- 235000013305 food Nutrition 0.000 description 5
- 229940068939 glyceryl monolaurate Drugs 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- XTJKNGLLPGBHHO-HNNXBMFYSA-N (2s)-5-(diaminomethylideneamino)-2-(dodecanoylamino)pentanoic acid Chemical compound CCCCCCCCCCCC(=O)N[C@H](C(O)=O)CCCN=C(N)N XTJKNGLLPGBHHO-HNNXBMFYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 4
- 241000894006 Bacteria Species 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 241000235342 Saccharomycetes Species 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 239000002671 adjuvant Substances 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 239000002537 cosmetic Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- 239000002609 medium Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- OMFXVFTZEKFJBZ-HJTSIMOOSA-N corticosterone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@H](CC4)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 OMFXVFTZEKFJBZ-HJTSIMOOSA-N 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- MGIYRDNGCNKGJU-UHFFFAOYSA-N isothiazolinone Chemical compound O=C1C=CSN1 MGIYRDNGCNKGJU-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000000813 microbial effect Effects 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- GHBFNMLVSPCDGN-UHFFFAOYSA-N rac-1-monooctanoylglycerol Chemical compound CCCCCCCC(=O)OCC(O)CO GHBFNMLVSPCDGN-UHFFFAOYSA-N 0.000 description 3
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- 229920001131 Pulp (paper) Polymers 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 235000013361 beverage Nutrition 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000004443 bio-dispersant Substances 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- 239000003139 biocide Substances 0.000 description 2
- RHDGNLCLDBVESU-UHFFFAOYSA-N but-3-en-4-olide Chemical compound O=C1CC=CO1 RHDGNLCLDBVESU-UHFFFAOYSA-N 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 239000012459 cleaning agent Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000008103 glucose Substances 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- 238000010412 laundry washing Methods 0.000 description 2
- 239000010985 leather Substances 0.000 description 2
- 238000005555 metalworking Methods 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000002453 shampoo Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000011885 synergistic combination Substances 0.000 description 2
- 150000003505 terpenes Chemical class 0.000 description 2
- 235000007586 terpenes Nutrition 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- VKZRWSNIWNFCIQ-WDSKDSINSA-N (2s)-2-[2-[[(1s)-1,2-dicarboxyethyl]amino]ethylamino]butanedioic acid Chemical compound OC(=O)C[C@@H](C(O)=O)NCCN[C@H](C(O)=O)CC(O)=O VKZRWSNIWNFCIQ-WDSKDSINSA-N 0.000 description 1
- OAAZUWWNSYWWHG-UHFFFAOYSA-N 1-phenoxypropan-1-ol Chemical compound CCC(O)OC1=CC=CC=C1 OAAZUWWNSYWWHG-UHFFFAOYSA-N 0.000 description 1
- PQHYOGIRXOKOEJ-UHFFFAOYSA-N 2-(1,2-dicarboxyethylamino)butanedioic acid Chemical compound OC(=O)CC(C(O)=O)NC(C(O)=O)CC(O)=O PQHYOGIRXOKOEJ-UHFFFAOYSA-N 0.000 description 1
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 241000700670 Bryozoa Species 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- 229920000858 Cyclodextrin Polymers 0.000 description 1
- 241000199914 Dinophyceae Species 0.000 description 1
- 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 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000233866 Fungi Species 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
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 241000237852 Mollusca Species 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000003619 algicide Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 230000008485 antagonism Effects 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 229940041514 candida albicans extract Drugs 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 229960001484 edetic acid Drugs 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- CUBZMGWLVMQKNE-LMOVPXPDSA-N ethyl (2s)-5-(diaminomethylideneamino)-2-(dodecanoylamino)pentanoate;hydrochloride Chemical compound Cl.CCCCCCCCCCCC(=O)N[C@H](C(=O)OCC)CCCNC(N)=N CUBZMGWLVMQKNE-LMOVPXPDSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000001087 glyceryl triacetate Substances 0.000 description 1
- 235000013773 glyceryl triacetate Nutrition 0.000 description 1
- 210000004349 growth plate Anatomy 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000012939 laminating adhesive Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 230000002906 microbiologic effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000001965 potato dextrose agar Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical class CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 238000001223 reverse osmosis Methods 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 238000013207 serial dilution Methods 0.000 description 1
- 235000015170 shellfish Nutrition 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000014347 soups Nutrition 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 229960002622 triacetin Drugs 0.000 description 1
- QCRXMFTZTSTGJM-UHFFFAOYSA-N triacetyl 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound CC(=O)OC(=O)CC(O)(C(=O)OC(C)=O)CC(=O)OC(C)=O QCRXMFTZTSTGJM-UHFFFAOYSA-N 0.000 description 1
- SZYJELPVAFJOGJ-UHFFFAOYSA-N trimethylamine hydrochloride Chemical compound Cl.CN(C)C SZYJELPVAFJOGJ-UHFFFAOYSA-N 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 238000012800 visualization Methods 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
- 239000012138 yeast extract Substances 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
-
- 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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/02—Acyclic compounds
-
- 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/04—Nitrogen directly attached to aliphatic or cycloaliphatic carbon atoms
-
- 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/12—Quaternary ammonium compounds
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group, wherein Cn means a carbon skeleton not containing a ring; Thio analogues thereof
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/46—N-acyl derivatives
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides
- A01N47/42—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides containing —N=CX2 groups, e.g. isothiourea
- A01N47/44—Guanidine; Derivatives thereof
-
- 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
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
- A01N59/16—Heavy metals; Compounds thereof
- A01N59/20—Copper
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Cosmetics (AREA)
Abstract
本发明涉及一种杀微生物剂组合物,其包含以下组分:(a)N-甲基-1,2-苯并异噻唑啉-3-酮;(b)2-氨基乙醇铜(II)和氯化二癸基二甲基铵。
Description
本申请是申请人于2008年7月16日提交的申请号为200810131638.3、发明名称为“杀微生物剂组合物”的发明专利申请的分案申请。
技术领域
本发明涉及选择的杀微生物剂的协同组合,所述组合的活性要大于在单独的杀微生物剂上观察到的活性。
背景技术
在一些情况下,由于市售的杀微生物剂对某些种类的微生物(例如对一些杀微生物剂具有抗性的微生物)的活性很差,或者由于剧烈的环境条件,即使采用高施用浓度,所述市售的杀微生物剂也无法提供有效的微生物控制。有时人们使用不同杀微生物剂的组合对特别的最终应用环境提供微生物的总体控制。例如,美国专利申请公开第2007/0078118号揭示了N-甲基-1,2-苯并异噻唑啉-3-酮(MBIT)与其它的生物杀伤剂的协同组合。但是,人们需要对各种微生物菌株具有提高的活性的另外的杀微生物剂的组合,以提供对微生物有效的控制。另外,出于环境和经济效益的考虑,人们需要包含较低含量单独的杀微生物剂的组合。本发明所解决的问题是提供这种杀微生物剂的另外的组合。
发明内容
本发明涉及包含以下组分的杀微生物剂组合物:(a)N-甲基-1,2-苯并异噻唑啉-3-酮;(b)选自以下的至少一种杀微生物剂:月桂酰精氨酸乙酯盐酸盐(ethyl lauroyl arginate hydrochloride)、氯化(柯卡酰氨丙基-N-2-羟基乙基氨基甲酰基甲基二甲基铵)(cocamidopropyl-N-2-hydroxyethylcarbamoylmethyl dimethyl ammonium chloride)、2-氨基乙醇铜(II)和氯化二癸基二甲基铵、碳酸二癸基二甲基铵和碳酸氢二癸基二甲基铵、2-氨基乙醇铜(II)、单月桂酸甘油酯、单月桂酸丙二醇酯、以及辛酸丙二醇酯。
具体实施方式
在本文中,除非上下文有另外的说明,以下术语具有所指的含意。“MBIT”是N-甲基-1,2-苯并异噻唑啉-3-酮。术语“杀微生物剂”表示能够在某一区域杀死微生物、抑制微生物生长或控制微生物生长的化合物;杀微生物剂包括杀菌剂,杀真菌剂和杀藻剂。术语“微生物”包括例如真菌(例如酵母菌和霉菌),细菌和藻类。术语“区域”表示易受微生物污染的工业装置或产品。在本说明书中使用以下缩写:ppm=百万分之一重量份(重量/重量),mL=毫升,ATCC=美国典型培养物保藏所(American Type CultureCollection),MIC=最低抑制浓度。除非另外说明,温度的单位是摄氏度(℃),百分数以重量计。有机杀微生物剂的含量以活性组分为基准计,单位为ppm(w/w)。
出乎意料地发现,本发明的组合物能够以低于单独的杀微生物剂的组合活性组分含量提供提高的杀微生物效率。在所述组合物中可以包含超出权利要求中所列范围的其它的杀微生物剂。
在本发明的一个实施方式中,所述抗微生物组合物包含N-甲基-1,2-苯并异噻唑啉-3-酮和月桂酰精氨酸乙酯盐酸盐。较佳的是,月桂酰精氨酸乙酯盐酸盐与N-甲基-1,2-苯并异噻唑啉-3-酮的重量比为1∶94至1∶0.0137。
在本发明的一个实施方式中,所述抗微生物组合物包含N-甲基-1,2-苯并异噻唑啉-3-酮和氯化(柯卡酰氨丙基-N-2-羟基乙基氨基甲酰基甲基二甲基铵)。较佳的是,氯化(柯卡酰氨丙基-N-2-羟基乙基氨基甲酰基甲基二甲基铵)与N-甲基-1,2-苯并异噻唑啉-3-酮的重量比为1∶188至1∶0.0022。
在本发明的一个实施方式中,所述抗微生物组合物包含N-甲基-1,2-苯并异噻唑啉-3-酮以及2-氨基乙醇铜(II)和氯化二癸基二甲基铵。较佳的是,2-氨基乙醇铜(II)和氯化二癸基二甲基铵与N-甲基-1,2-苯并异噻唑啉-3-酮的重量比为1∶176至1∶0.08。
在本发明的一个实施方式中,所述抗微生物组合物包含N-甲基-1,2-苯并异噻唑啉-3-酮以及碳酸二癸基二甲基铵和碳酸氢二癸基二甲基铵。较佳的是,碳酸二癸基二甲基铵和碳酸氢二癸基二甲基铵与N-甲基-1,2-苯并异噻唑啉-3-酮的重量比为1∶227至1∶0.179。
在本发明的一个实施方式中,所述抗微生物组合物包含N-甲基-1,2-苯并异噻唑啉-3-酮和2-氨基乙醇铜(II)。较佳的是,2-氨基乙醇铜(II)与N-甲基-1,2-苯并异噻唑啉-3-酮的重量比为1∶375至1∶0.004。
在本发明的一个实施方式中,所述抗微生物组合物包含N-甲基-1,2-苯并异噻唑啉-3-酮和单月桂酸甘油酯。较佳的是,单月桂酸甘油酯与N-甲基-1,2-苯并异噻唑啉-3-酮的重量比为1∶0.143至1∶0.0004。
在本发明的一个实施方式中,所述抗微生物组合物包含N-甲基-1,2-苯并异噻唑啉-3-酮和单月桂酸丙二醇酯。较佳的是,单月桂酸丙二醇酯与N-甲基-1,2-苯并异噻唑啉-3-酮的重量比为1∶0.286至1∶0.0286。
在本发明的一个实施方式中,所述抗微生物组合物包含N-甲基-1,2-苯并异噻唑啉-3-酮和辛酸丙二醇酯。较佳的是,辛酸丙二醇酯与N-甲基-1,2-苯并异噻唑啉-3-酮的重量比为1∶0.442至1∶0.0018。
本发明组合物中的杀微生物剂可直接使用,或者可首先使用溶剂或固体载体进行配制。合适的溶剂包括例如水;二元醇,例如乙二醇、丙二醇、二甘醇、二丙甘醇、聚乙二醇和聚丙二醇;乙二醇醚;醇,例如甲醇、乙醇、丙醇、苯乙醇和苯氧基丙醇;酮,例如丙酮和甲基乙基酮;酯,例如乙酸乙酯、乙酸丁酯、三乙酰基柠檬酸酯、以及三乙酸甘油酯;碳酸酯,例如碳酸异丙烯酯和碳酸二甲酯;以及它们的混合物。优选的溶剂选自水、二元醇、二醇醚、酯及其混合物。合适的固体载体包括例如环糊精、二氧化硅、硅藻土、蜡、纤维素材料、碱金属和碱土(例如钠、镁、钾)金属盐(例如氯化物、硝酸盐、溴化物、硫酸盐)和炭。
当杀微生物剂用溶剂配制时,该制剂可任选包含表面活性剂。当这种制剂包含表面活性剂时,它们通常为乳液浓缩物、乳液、微乳液浓缩物或微乳液的形式。乳液浓缩物在加入足量的水的时候形成乳液。微乳液浓缩物在加入足量的水的时候形成微乳液。这些乳液和微乳液浓缩物是本领域众所周知的;优选这些制剂不含表面活性剂。关于制备各种微乳液和微乳液浓缩物的更广泛和具体的细节可参见美国专利第5444078号。
还可以分散体的形式配制杀微生物剂组分。分散体的溶剂组分可以是有机溶剂或水,优选的是水。这些分散体可包含辅助剂,例如助溶剂、增稠剂、防冻剂、分散剂、填料、颜料、表面活性剂、生物分散剂、磺基丁二酸盐、萜烯、呋喃酮、聚阳离子、稳定剂、污垢抑制剂和抗腐蚀添加剂。
当两种杀微生物剂都各自先用溶剂配制时,用于第一杀微生物剂的溶剂可与用来配制另一种市售杀微生物剂的溶剂相同或不同,但是优选水用于大多数工业生物杀伤剂应用。较佳的是,这两种溶剂可混溶。
本领域技术人员将会意识到,可以将本发明的杀微生物剂依次或同时施加到某一区域,或者在施加到该区域之前混合。较佳的是,将第一杀微生物剂和第二杀微生物剂同时或依次施加到某一区域。当所述杀微生物剂同时或依次施加到某区域时,每种单独的组分可包含辅助剂,例如溶剂、增稠剂、防冻剂、着色剂、螯合剂(例如乙二胺四乙酸、乙二胺二琥珀酸、亚氨基二琥珀酸及其盐)、分散剂、表面活性剂、生物分散剂、磺基丁二酸酯、萜烯、呋喃酮、聚阳离子、稳定剂、污垢抑制剂和抗腐蚀添加剂。
可通过在易受微生物侵袭的区域上或之内引入抗菌有效量的本发明杀微生物组合物来抑制微生物或者更高级的水生生物(例如原生动物,无脊椎动物,苔藓动物,腰鞭毛类,甲壳类动物,软体动物等)的生长。合适的区域包括例如:工业工艺水;电涂覆沉积系统;冷却塔;空气洗涤器;气体洗涤器;矿物浆液;废水处理系统;装饰用喷泉;反渗透过滤器;超滤装置;压舱水;蒸发冷凝器;热交换器;纸浆和纸加工液以及添加剂;淀粉;塑料;乳液;分散体;油漆;胶乳;涂料,例如清漆;建筑产品,例如胶泥、填漏材料和密封剂;建筑粘合剂,例如陶瓷粘合剂、地毯背衬粘合剂和层叠粘合剂;工业用或消费用粘合剂;摄影用化学品;印刷液;家用产品,例如卫生间和厨房清洁剂以及清洁擦拭用品;化妆品;化妆用品;洗发露;肥皂;洗涤剂;工业清洁剂;地板蜡;洗衣房漂洗水;金属加工液;输送带润滑剂;液压机液体;皮革和皮革制品;织物;织物产品;木材和木材产品,例如胶合板、硬纸板、刨花板、叠层梁、取向的绞合板、硬纸板和碎料板;石油加工液;燃料;油田液,例如注入水、断裂液和钻探泥浆;农业辅助剂保存;表面活性剂保存;医疗器件;诊断试剂保存;食物保存,例如塑料或纸质食物包装;食物、饮料、以及工业处理巴氏灭菌器;抽水马桶;娱乐用水;池塘;和温泉。
优选用本发明的杀微生物剂组合物在选自以下的一个或多个区域抑制微生物的生长:矿物浆液;纸浆和纸加工液以及添加剂;淀粉;乳液;分散体;油漆;胶乳;涂料;建筑粘合剂,例如陶瓷粘合剂、地毯背衬粘合剂;摄影用化学品;印刷液;家用产品,例如卫生间和厨房清洁剂以及清洁擦拭用品;化妆品;化妆用品;洗发露;肥皂;洗涤剂;工业清洁剂;地板蜡;洗衣房漂洗水;金属加工液;织物产品;木材和木材产品;农业辅助剂保存;表面活性剂保存;诊断试剂保存;食物保存;食物、饮料、以及工业程序的巴氏灭菌器。
用来抑制或控制某一区域微生物生长所需的本发明组合物的具体用量取决于需要保护的特定区域。通常来说,如果在某区域中提供的本发明组合物的异噻唑啉酮组分含量为0.1-1000ppm,则该组合物的量足以控制微生物生长。较佳的是在该区域中组合物的异噻唑啉酮组分含量至少为0.5ppm,更优选至少为4ppm,最优选至少为10ppm。较佳的是存在于该区域中的组合物的异噻唑啉酮组分的含量不超过1000ppm,更优选不超过500ppm,最优选不超过200ppm。
实施例
材料和方法
通过对宽范围的化合物浓度和比例进行测试,说明了本发明的组合的协同作用。
一种协同作用的测定是Kull,F.C.;Eisman,P.C.;Sylwestrowicz,H.D.和Mayer,R.L.在应用微生物学(Applied Microbiology)9:538-541(1961)中提出的工业可接受的方法,该方法使用由下式算得的比例:
Qa/QA+Qb/QB=协同指数(“SI”)
式中:
QA=单用时能够产生终点的化合物A(第一组分)的浓度(化合物A的MIC),其单位为ppm。
Qa=以混合物形式时能够产生终点的化合物A的浓度,其单位为ppm。
QB=单用时能够产生终点的化合物B(第二组分)的浓度(化合物B的MIC),其单位为ppm。
Qb=以混合物形式时能够产生终点的化合物B的浓度,其单位为ppm。
当Qa/QA和Qb/QB之和大于1时,说明具有拮抗作用。当它们之和等于1时,说明具有叠加作用,当小于1时,说明具有协同作用。SI越小,特定混合物所显示的协同作用越大。抗菌化合物的最小抑制浓度(MIC)是在一组特定条件下测得的能够阻止所加入的微生物生长的最低浓度。
使用标准微量滴定板,用设计能使试验微生物最优生长的培养基进行协同试验。细菌试验采用添加了0.2%葡萄糖和0.1%的酵母提取物的矿物盐培养基(M9GY培养基);酵母菌和霉菌试验使用马铃薯葡萄糖肉汤(PotatoDextrose Broth)(PDB培养基)。在此方法中,在包含各种浓度的MBIT的情况下进行高分辨MIC试验检测了许多种杀微生物剂的组合。高分辨MIC通过以下步骤进行:在一排微量滴定板中加入各种量的杀微生物剂,用自动液体操作系统进行10倍连续稀释,获得从2ppm至10000ppm活性组分的一系列活性组分的终点。
测定了本发明的组合下表所述的一些微生物的协同作用。所用细菌的浓度约为5×106细菌/毫升,酵母菌和霉菌的浓度为5×105真菌/毫升。这些微生物代表了许多消费品和工业应用中的天然污染。在25℃(酵母菌和霉菌)或30℃(细菌)培养不同时间后目视观察微量滴定板上微生物生长情况确定MIC。
显示本发明MBIT组合的协同作用的试验结果列于以下表1-8中。在各测试中,第二组分(B)是MBIT,第一组分(A)是其它的市售杀微生物剂。各表显示了MBIT和其它组分的具体组合;在培育时间测得的对抗微生物的结果;通过MIC测定单用MBIT(QB),单用其它组分(QA),在混合物中的MBIT(Qb)以及在混合物中的其它组分(Qa)的终点活性,单位为ppm;计算的SI值;以及各种被测组合的协同比范围(其它组分/MBlT或者A/B)。
表1
Ca:CYTO GUARD LA(月桂酰精氨酸乙酯盐酸盐)的ppm AI
Cb:MBIT(N-甲基-1,2-苯并异噻唑啉-3-酮)的ppm AI
比例:Ca∶Cb
表2
Ca:MONTALINE C40(氯化(柯卡酰氨丙基-N-2-羟基乙基氨基甲酰基甲基二甲基铵))的ppm AI
Cb:MBIT(N-甲基-1,2-苯并异噻唑啉-3-酮)的ppm AI
比例:Ca∶Cb
表3
Ca:ACQ D型(2-氨基乙醇铜(II)&氯化二癸基二甲基铵)的ppm AI(ppm CuO)
Cb:MBIT(N-甲基-1,2-苯并异噻唑啉-3-酮)的ppm AI
比例:Ca∶Cb
表4
Ca:CARBOQUAT WP-50(碳酸二癸基二甲基铵和碳酸氢二癸基二甲基铵)的ppm AI
Cb:MBIT(N-甲基-1,2-苯并异噻唑啉-3-酮)的ppm AI
比例:Ca∶Cb
表5
Ca:ACQ C2(2-氨基乙醇铜(II))的ppm AI
Cb:MBIT(N-甲基-1,2-苯并异噻唑啉-3-酮)的ppm AI
比例:Ca∶Cb
表6
Ca:CAPMUL GML(单月桂酸甘油酯)的ppm AI
Cb:MBIT(N-甲基-1,2-苯并异噻唑啉-3-酮)的ppm AI
比例:Ca∶Cb
表:7
Ca:CAPMUL PG12(单月桂酸丙二醇酯)的ppm AI
Cb:MBIT(N-甲基-1,2-苯并异噻唑啉-3-酮)的ppm AI
比例:Ca∶Cb
表:8
Ca:Capmul PG8(辛酸丙二醇酯)的ppm AI
Cb:MBIT(N-甲基-1,2-苯并异噻唑啉-3-酮)的ppm AI
比例:Ca∶Cb
Claims (1)
1.一种杀微生物剂组合物,其包含以下组分:
(a)N-甲基-1,2-苯并异噻唑啉-3-酮;
(b)2-氨基乙醇铜(II)和氯化二癸基二甲基铵,2-氨基乙醇铜(II)和氯化二癸基二甲基铵与N-甲基-1,2-苯并异噻唑啉-3-酮之比为1:176至1:0.1200。
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07290902.1 | 2007-07-18 | ||
| EP07290902 | 2007-07-18 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2008101316383A Division CN101347119B (zh) | 2007-07-18 | 2008-07-16 | 杀微生物剂组合物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102308811A CN102308811A (zh) | 2012-01-11 |
| CN102308811B true CN102308811B (zh) | 2014-01-22 |
Family
ID=39405379
Family Applications (7)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201110230502.XA Expired - Fee Related CN102308811B (zh) | 2007-07-18 | 2008-07-16 | 杀微生物剂组合物 |
| CN2008101316383A Expired - Fee Related CN101347119B (zh) | 2007-07-18 | 2008-07-16 | 杀微生物剂组合物 |
| CN201110229072.XA Expired - Fee Related CN102318613B (zh) | 2007-07-18 | 2008-07-16 | 杀微生物剂组合物 |
| CN201110230484.5A Expired - Fee Related CN102308810B (zh) | 2007-07-18 | 2008-07-16 | 杀微生物剂组合物 |
| CN201110229044.8A Expired - Fee Related CN102302013B (zh) | 2007-07-18 | 2008-07-16 | 杀微生物剂组合物 |
| CN2011102290838A Expired - Fee Related CN102265839B (zh) | 2007-07-18 | 2008-07-16 | 杀微生物剂组合物 |
| CN2011102290857A Expired - Fee Related CN102302014B (zh) | 2007-07-18 | 2008-07-16 | 杀微生物剂组合物 |
Family Applications After (6)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2008101316383A Expired - Fee Related CN101347119B (zh) | 2007-07-18 | 2008-07-16 | 杀微生物剂组合物 |
| CN201110229072.XA Expired - Fee Related CN102318613B (zh) | 2007-07-18 | 2008-07-16 | 杀微生物剂组合物 |
| CN201110230484.5A Expired - Fee Related CN102308810B (zh) | 2007-07-18 | 2008-07-16 | 杀微生物剂组合物 |
| CN201110229044.8A Expired - Fee Related CN102302013B (zh) | 2007-07-18 | 2008-07-16 | 杀微生物剂组合物 |
| CN2011102290838A Expired - Fee Related CN102265839B (zh) | 2007-07-18 | 2008-07-16 | 杀微生物剂组合物 |
| CN2011102290857A Expired - Fee Related CN102302014B (zh) | 2007-07-18 | 2008-07-16 | 杀微生物剂组合物 |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US8129419B2 (zh) |
| EP (8) | EP2338337B1 (zh) |
| JP (5) | JP4944844B2 (zh) |
| KR (8) | KR101111639B1 (zh) |
| CN (7) | CN102308811B (zh) |
| AT (1) | ATE527879T1 (zh) |
| AU (1) | AU2008203010B2 (zh) |
| BR (8) | BRPI0803669B1 (zh) |
| CA (4) | CA2724727C (zh) |
| CL (7) | CL2008002094A1 (zh) |
| ES (4) | ES2421003T3 (zh) |
| MX (1) | MX2008009222A (zh) |
| NO (8) | NO340805B1 (zh) |
| NZ (7) | NZ590808A (zh) |
| PL (5) | PL2338338T3 (zh) |
| TW (8) | TWI410215B (zh) |
| ZA (1) | ZA200806097B (zh) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4944843B2 (ja) * | 2007-07-18 | 2012-06-06 | ローム アンド ハース カンパニー | 殺微生物組成物 |
| JP2009149610A (ja) * | 2007-12-20 | 2009-07-09 | Rohm & Haas Co | 相乗的殺微生物性組成物 |
| DE102010009852A1 (de) * | 2010-03-02 | 2011-09-08 | Kalle Gmbh | Antimikrobiell ausgerüstete Folien, Schwämme und Schwammtücher |
| DE102010013274A1 (de) * | 2010-03-29 | 2011-11-17 | Beiersdorf Ag | Mikrobiologisch stabile anwendungsfreundliche Zubereitungen |
| LT2632267T (lt) * | 2010-10-25 | 2016-12-27 | Lanxess Deutschland Gmbh | Fungicidiniai penfufeno mišiniai |
| EP2760287B1 (en) * | 2011-09-30 | 2020-01-08 | Kemira OYJ | Prevention of starch degradation in pulp, paper or board making processes |
| CN102416011A (zh) * | 2011-10-10 | 2012-04-18 | 艾硕特生物科技(昆明)有限公司 | 一种广谱、高效的抗菌洗液 |
| MX2015016675A (es) * | 2013-06-04 | 2016-07-15 | Vyome Biosciences Pvt Ltd | Particulas recubiertas y composiciones que comprenden las mismas. |
| GB2515473A (en) * | 2013-06-18 | 2014-12-31 | Robert Timothy Gros | Anti microbial inks and sealants |
| KR101525987B1 (ko) * | 2015-02-12 | 2015-06-08 | 주식회사 명진뉴텍 | 물티슈 조성물 및 이를 포함하는 물티슈 |
| CN105660659B (zh) * | 2016-01-11 | 2018-08-28 | 江苏辉丰农化股份有限公司 | 一种杀菌剂组合物 |
| WO2017222963A1 (en) * | 2016-06-24 | 2017-12-28 | Lonza Inc. | Synergistic antimicrobial combinations containing quaternary ammonium biocide |
| KR101843686B1 (ko) | 2017-06-20 | 2018-03-29 | 고려대학교 산학협력단 | 분리막용 비산화성 살균제 및 이를 이용한 분리막의 살균 방법 |
| FR3068213B1 (fr) * | 2017-06-30 | 2019-08-16 | L'oreal | Melange antimicrobien contenant du 4-(3-ethoxy-4-hydroxyphenyl)butan-2-one et un compose arginate, et composition cosmetique le contenant |
| RU2020106392A (ru) | 2017-07-19 | 2021-08-19 | Криовак, Ллк | Противомикробные упаковочные пленки |
| JP6978766B2 (ja) * | 2017-08-10 | 2021-12-08 | 住化エンバイロメンタルサイエンス株式会社 | 切り花延命剤 |
| KR102061111B1 (ko) * | 2017-08-14 | 2020-02-20 | 주식회사 일신웰스 | 항균 조성물 및 이의 제조방법 |
| US12029773B2 (en) | 2018-05-14 | 2024-07-09 | Barentz North America, Llc | Mastic-derived natural protectants |
| CN112899087B (zh) * | 2018-06-22 | 2022-07-08 | 华东师范大学 | 厨房油污清洗剂 |
| CA3190534A1 (en) * | 2020-08-31 | 2022-03-03 | Salvacion Usa Inc. | Antiviral composition and use of the same |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006118980A2 (en) * | 2005-05-04 | 2006-11-09 | Viance, Llc. | Long-chain quaternary ammonium compounds as wood treatment agents |
| EP1733616A2 (en) * | 2005-06-15 | 2006-12-20 | Rohm and Haas Company | Antimicrobial composition useful for preserving wood |
Family Cites Families (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1352420A (en) | 1971-06-18 | 1974-05-08 | Ajinomoto Kk | Arginine derivatives their production and their use |
| US4067997A (en) * | 1975-05-21 | 1978-01-10 | Med-Chem Laboratories | Synergistic microbecidal composition and method |
| JPS59164704A (ja) | 1983-03-09 | 1984-09-17 | Lion Corp | 防腐防カビ剤 |
| JPH01107121A (ja) | 1987-10-20 | 1989-04-25 | Yotaro Hatamura | 荷重検出器 |
| DE3807070A1 (de) * | 1988-03-04 | 1989-09-14 | Hoechst Ag | Schlauchfoermige nahrungsmittelhuelle aus cellulosehydrat, insbesondere kuenstliche wursthuelle |
| GB8907298D0 (en) * | 1989-03-31 | 1989-05-17 | Ici Plc | Composition and use |
| US5438034A (en) * | 1993-06-09 | 1995-08-01 | Lonza, Inc. | Quaternary ammonium carbonate compositions and preparation thereof |
| CA2169559C (en) * | 1993-09-14 | 2004-11-30 | Jeffrey F. Andrews | Disinfectant composition |
| US5444078A (en) | 1993-10-01 | 1995-08-22 | Rohm And Haas Company | Fully water-dilutable microemulsions |
| FR2721607B1 (fr) * | 1994-06-28 | 1996-10-31 | Seppic Sa | Nouveaux dérivés d'ammoniums quaternaires, leur procédé de préparation et leur utilisation comme agents de surface. |
| DE19548710A1 (de) * | 1995-12-23 | 1997-06-26 | Riedel De Haen Ag | Konservierungsmittel, enthaltend Isothiazolinon-Derivate und Komplexbildner |
| ES2185155T3 (es) * | 1997-03-06 | 2003-04-16 | Wolman Gmbh Dr | Agentes conservantes de madera para la proteccion subsiguiente. |
| JPH10298012A (ja) * | 1997-04-22 | 1998-11-10 | Takeda Chem Ind Ltd | 殺微生物剤組成物および微生物防除方法 |
| JPH1171211A (ja) * | 1997-09-01 | 1999-03-16 | Takeda Chem Ind Ltd | 工業用殺菌剤および殺菌方法 |
| AU761563B2 (en) * | 1999-05-21 | 2003-06-05 | 3M Innovative Properties Company | Antimicrobial articles |
| BR0015806A (pt) * | 1999-11-24 | 2003-07-15 | 3M Innovative Properties Co | Formulação antimicrobiana, método para a redução de nìveis microbianos em plantas ou partes de plantas, conjunto, artigo de manufatura, e, planta ou parte de planta |
| JP2001150404A (ja) * | 1999-11-26 | 2001-06-05 | Xyence Corp | 銅系木材保存用組成物 |
| JP4809514B2 (ja) * | 2000-02-29 | 2011-11-09 | 大日本木材防腐株式会社 | 非塩素系木材防腐剤 |
| US20040208842A1 (en) * | 2001-09-18 | 2004-10-21 | Ritchie Branson W. | Antimicrobial cleansing compositions and methods of use |
| BR0111415B1 (pt) | 2001-04-28 | 2012-12-11 | composição antimicrobiana compreendendo sorbato de potássio e lae. | |
| CA2455983C (en) * | 2001-08-09 | 2010-06-01 | Joan Baptista Urgell Beltran | Preservative systems and their use in cosmetic preparations |
| AU2004201059B2 (en) | 2003-03-26 | 2009-06-04 | Rohm And Haas Company | Microbicidal composition |
| JP4498794B2 (ja) * | 2004-03-26 | 2010-07-07 | 株式会社パーマケム・アジア | ウエット状態の繊維または紙製品に用いられる防菌防黴剤 |
| US20050227956A1 (en) * | 2004-04-13 | 2005-10-13 | Ying Wang | Control of mold growth on wood |
| SI21885B (sl) * | 2004-09-17 | 2009-10-31 | Košmerl Stojan | Sredstvo za zaščito lesa |
| JP2006273719A (ja) | 2005-03-28 | 2006-10-12 | Adeka Corp | 抗菌剤組成物 |
| EP1906734A1 (en) | 2005-07-11 | 2008-04-09 | Thor Specialities (UK) Lmited | Microbiocidal composition |
| US20070014740A1 (en) * | 2005-07-15 | 2007-01-18 | Colgate-Palmolive Company | Oral compositions having cationic active ingredients |
| DE102005045129A1 (de) * | 2005-09-21 | 2007-03-22 | Schülke & Mayr GmbH | Zubereitung zur fungiziden und algiziden Ausrüstung alkalischer Beschichtungszusammensetzungen |
| EP1772055A1 (en) * | 2005-10-04 | 2007-04-11 | Rohm and Haas France SAS | Synergistic microbicidal compositions comprising a N-alkyl-1,2-benzoisothiazolin-3-one |
| CA2610046C (en) * | 2006-11-22 | 2011-04-26 | Rohm And Haas Company | Antimicrobial composition useful for preserving wood |
| JP4944843B2 (ja) * | 2007-07-18 | 2012-06-06 | ローム アンド ハース カンパニー | 殺微生物組成物 |
-
2008
- 2008-07-04 JP JP2008175527A patent/JP4944844B2/ja not_active Expired - Fee Related
- 2008-07-08 TW TW101121500A patent/TWI410215B/zh not_active IP Right Cessation
- 2008-07-08 TW TW101121496A patent/TWI417049B/zh not_active IP Right Cessation
- 2008-07-08 NZ NZ590808A patent/NZ590808A/en not_active IP Right Cessation
- 2008-07-08 US US12/217,692 patent/US8129419B2/en not_active Expired - Fee Related
- 2008-07-08 TW TW101121501A patent/TWI410216B/zh not_active IP Right Cessation
- 2008-07-08 AU AU2008203010A patent/AU2008203010B2/en not_active Ceased
- 2008-07-08 NZ NZ590810A patent/NZ590810A/en not_active IP Right Cessation
- 2008-07-08 TW TW101121502A patent/TWI410217B/zh not_active IP Right Cessation
- 2008-07-08 TW TW097125654A patent/TWI399174B/zh not_active IP Right Cessation
- 2008-07-08 TW TW101121503A patent/TWI426865B/zh not_active IP Right Cessation
- 2008-07-08 NZ NZ590806A patent/NZ590806A/en not_active IP Right Cessation
- 2008-07-08 NZ NZ590805A patent/NZ590805A/en not_active IP Right Cessation
- 2008-07-08 TW TW101121499A patent/TWI418300B/zh not_active IP Right Cessation
- 2008-07-08 TW TW101121498A patent/TWI417047B/zh not_active IP Right Cessation
- 2008-07-08 NZ NZ569668A patent/NZ569668A/en not_active IP Right Cessation
- 2008-07-08 NZ NZ580809A patent/NZ580809A/en not_active IP Right Cessation
- 2008-07-08 NZ NZ590807A patent/NZ590807A/en not_active IP Right Cessation
- 2008-07-09 CA CA2724727A patent/CA2724727C/en not_active Expired - Fee Related
- 2008-07-09 NO NO20083086A patent/NO340805B1/no not_active IP Right Cessation
- 2008-07-09 CA CA2724724A patent/CA2724724C/en not_active Expired - Fee Related
- 2008-07-09 CA CA2637129A patent/CA2637129C/en not_active Expired - Fee Related
- 2008-07-09 CA CA2724719A patent/CA2724719C/en not_active Expired - Fee Related
- 2008-07-14 ZA ZA200806097A patent/ZA200806097B/en unknown
- 2008-07-15 KR KR1020080068470A patent/KR101111639B1/ko not_active Expired - Fee Related
- 2008-07-16 CN CN201110230502.XA patent/CN102308811B/zh not_active Expired - Fee Related
- 2008-07-16 CN CN2008101316383A patent/CN101347119B/zh not_active Expired - Fee Related
- 2008-07-16 BR BRPI0803669A patent/BRPI0803669B1/pt not_active IP Right Cessation
- 2008-07-16 BR BR122015027160A patent/BR122015027160B1/pt active IP Right Grant
- 2008-07-16 BR BR122015027157A patent/BR122015027157B1/pt active IP Right Grant
- 2008-07-16 CN CN201110229072.XA patent/CN102318613B/zh not_active Expired - Fee Related
- 2008-07-16 CN CN201110230484.5A patent/CN102308810B/zh not_active Expired - Fee Related
- 2008-07-16 CN CN201110229044.8A patent/CN102302013B/zh not_active Expired - Fee Related
- 2008-07-16 BR BR122015027162A patent/BR122015027162B1/pt active IP Right Grant
- 2008-07-16 BR BR122015027155A patent/BR122015027155B1/pt active IP Right Grant
- 2008-07-16 BR BR122015027159A patent/BR122015027159B1/pt active IP Right Grant
- 2008-07-16 BR BR122015027163A patent/BR122015027163B1/pt active IP Right Grant
- 2008-07-16 CN CN2011102290838A patent/CN102265839B/zh not_active Expired - Fee Related
- 2008-07-16 BR BR122015027161A patent/BR122015027161B1/pt active IP Right Grant
- 2008-07-16 CN CN2011102290857A patent/CN102302014B/zh not_active Expired - Fee Related
- 2008-07-17 MX MX2008009222A patent/MX2008009222A/es active IP Right Grant
- 2008-07-17 EP EP11161691.8A patent/EP2338337B1/en not_active Not-in-force
- 2008-07-17 EP EP11161696.7A patent/EP2338340B1/en not_active Not-in-force
- 2008-07-17 EP EP08160663A patent/EP2016827B1/en not_active Not-in-force
- 2008-07-17 ES ES11161691T patent/ES2421003T3/es active Active
- 2008-07-17 PL PL11161692T patent/PL2338338T3/pl unknown
- 2008-07-17 EP EP11161694.2A patent/EP2338339B1/en not_active Not-in-force
- 2008-07-17 EP EP11161692.6A patent/EP2338338B1/en not_active Not-in-force
- 2008-07-17 ES ES11161692T patent/ES2417014T3/es active Active
- 2008-07-17 EP EP11161690.0A patent/EP2338336B1/en not_active Not-in-force
- 2008-07-17 EP EP11161693.4A patent/EP2340711B1/en not_active Not-in-force
- 2008-07-17 ES ES11161690T patent/ES2418579T3/es active Active
- 2008-07-17 AT AT08160663T patent/ATE527879T1/de not_active IP Right Cessation
- 2008-07-17 EP EP11161695.9A patent/EP2340712B1/en not_active Not-in-force
- 2008-07-17 PL PL11161693T patent/PL2340711T3/pl unknown
- 2008-07-17 PL PL11161690T patent/PL2338336T3/pl unknown
- 2008-07-17 PL PL11161694T patent/PL2338339T3/pl unknown
- 2008-07-17 PL PL11161691T patent/PL2338337T3/pl unknown
- 2008-07-17 CL CL2008002094A patent/CL2008002094A1/es unknown
- 2008-07-17 ES ES11161693T patent/ES2421004T3/es active Active
-
2010
- 2010-11-11 KR KR1020100111829A patent/KR101102491B1/ko not_active Expired - Fee Related
- 2010-11-11 KR KR1020100111834A patent/KR101073483B1/ko not_active Expired - Fee Related
- 2010-11-11 KR KR1020100111831A patent/KR101073452B1/ko not_active Expired - Fee Related
- 2010-11-11 KR KR1020100111833A patent/KR101073481B1/ko not_active Expired - Fee Related
- 2010-11-11 KR KR1020100111832A patent/KR101073480B1/ko not_active Expired - Fee Related
- 2010-11-11 KR KR1020100111835A patent/KR101073484B1/ko not_active Expired - Fee Related
- 2010-11-11 KR KR1020100111842A patent/KR101073489B1/ko not_active Expired - Fee Related
-
2011
- 2011-08-11 JP JP2011176068A patent/JP5390570B2/ja not_active Expired - Fee Related
- 2011-08-11 JP JP2011176069A patent/JP5389870B2/ja not_active Expired - Fee Related
- 2011-08-11 JP JP2011176071A patent/JP5389872B2/ja not_active Expired - Fee Related
- 2011-08-11 JP JP2011176070A patent/JP5389871B2/ja not_active Expired - Fee Related
-
2013
- 2013-01-21 CL CL2013000189A patent/CL2013000189A1/es unknown
- 2013-01-21 CL CL2013000193A patent/CL2013000193A1/es unknown
- 2013-01-21 CL CL2013000194A patent/CL2013000194A1/es unknown
- 2013-01-21 CL CL2013000195A patent/CL2013000195A1/es unknown
- 2013-01-21 CL CL2013000190A patent/CL2013000190A1/es unknown
- 2013-01-21 CL CL2013000191A patent/CL2013000191A1/es unknown
-
2017
- 2017-01-27 NO NO20170125A patent/NO340983B1/no not_active IP Right Cessation
- 2017-01-27 NO NO20170123A patent/NO340985B1/no not_active IP Right Cessation
- 2017-01-27 NO NO20170130A patent/NO340980B1/no not_active IP Right Cessation
- 2017-01-27 NO NO20170126A patent/NO340982B1/no not_active IP Right Cessation
- 2017-01-27 NO NO20170124A patent/NO340984B1/no not_active IP Right Cessation
- 2017-01-27 NO NO20170128A patent/NO340981B1/no not_active IP Right Cessation
- 2017-01-27 NO NO20170132A patent/NO340977B1/no not_active IP Right Cessation
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006118980A2 (en) * | 2005-05-04 | 2006-11-09 | Viance, Llc. | Long-chain quaternary ammonium compounds as wood treatment agents |
| EP1733616A2 (en) * | 2005-06-15 | 2006-12-20 | Rohm and Haas Company | Antimicrobial composition useful for preserving wood |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN102308811B (zh) | 杀微生物剂组合物 | |
| CN102090402B (zh) | 杀微生物组合物 | |
| CN102318615B (zh) | 杀微生物剂组合物 | |
| CN102293206B (zh) | 杀微生物组合物 | |
| CN103548867A (zh) | 协同杀微生物组合物 | |
| CN104270947A (zh) | 杀微生物组合物 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20140122 Termination date: 20170716 |
|
| CF01 | Termination of patent right due to non-payment of annual fee |