JPH11506103A - Ｎ−アルキルヘテロ環化合物を用いた殺菌効果の活性化 - Google Patents
Ｎ−アルキルヘテロ環化合物を用いた殺菌効果の活性化Info
- Publication number
- JPH11506103A JPH11506103A JP8536575A JP53657596A JPH11506103A JP H11506103 A JPH11506103 A JP H11506103A JP 8536575 A JP8536575 A JP 8536575A JP 53657596 A JP53657596 A JP 53657596A JP H11506103 A JPH11506103 A JP H11506103A
- Authority
- JP
- Japan
- Prior art keywords
- dodecyl
- microbicide
- growth
- methyl
- microorganisms
- 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.)
- Ceased
Links
- 150000001875 compounds Chemical class 0.000 title claims abstract description 105
- 230000000844 anti-bacterial effect Effects 0.000 title description 11
- 230000004913 activation Effects 0.000 title description 2
- 230000003641 microbiacidal effect Effects 0.000 claims abstract description 162
- 229940124561 microbicide Drugs 0.000 claims abstract description 130
- 244000005700 microbiome Species 0.000 claims abstract description 110
- 239000002855 microbicide agent Substances 0.000 claims abstract description 96
- 238000000034 method Methods 0.000 claims abstract description 85
- 239000000203 mixture Substances 0.000 claims abstract description 39
- 239000000758 substrate Substances 0.000 claims abstract description 27
- 239000002023 wood Substances 0.000 claims abstract description 27
- 239000004753 textile Substances 0.000 claims abstract description 19
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 11
- 239000010985 leather Substances 0.000 claims abstract description 8
- 230000002708 enhancing effect Effects 0.000 claims abstract description 6
- 239000000463 material Substances 0.000 claims description 24
- 241000233866 Fungi Species 0.000 claims description 16
- 230000002401 inhibitory effect Effects 0.000 claims description 15
- JMTFLSQHQSFNTE-UHFFFAOYSA-N 1-dodecylimidazole Chemical compound CCCCCCCCCCCCN1C=CN=C1 JMTFLSQHQSFNTE-UHFFFAOYSA-N 0.000 claims description 14
- 241000894006 Bacteria Species 0.000 claims description 14
- BSWWXRFVMJHFBN-UHFFFAOYSA-N 2,4,6-tribromophenol Chemical compound OC1=C(Br)C=C(Br)C=C1Br BSWWXRFVMJHFBN-UHFFFAOYSA-N 0.000 claims description 12
- ZRIILUSQBDFVNY-UHFFFAOYSA-N 4-dodecylmorpholine Chemical compound CCCCCCCCCCCCN1CCOCC1 ZRIILUSQBDFVNY-UHFFFAOYSA-N 0.000 claims description 12
- -1 2-pyrrolidinonyl Chemical group 0.000 claims description 11
- DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 claims description 11
- 241000195493 Cryptophyta Species 0.000 claims description 9
- DHNRXBZYEKSXIM-UHFFFAOYSA-N chloromethylisothiazolinone Chemical group CN1SC(Cl)=CC1=O DHNRXBZYEKSXIM-UHFFFAOYSA-N 0.000 claims description 9
- 229940100484 5-chloro-2-methyl-4-isothiazolin-3-one Drugs 0.000 claims description 8
- 239000000839 emulsion Substances 0.000 claims description 8
- RCVKZMQGFZRHKO-UHFFFAOYSA-N 1-iodoprop-2-ynyl carbamate Chemical compound NC(=O)OC(I)C#C RCVKZMQGFZRHKO-UHFFFAOYSA-N 0.000 claims description 7
- LVDKZNITIUWNER-UHFFFAOYSA-N Bronopol Chemical compound OCC(Br)(CO)[N+]([O-])=O LVDKZNITIUWNER-UHFFFAOYSA-N 0.000 claims description 7
- 150000002391 heterocyclic compounds Chemical class 0.000 claims description 7
- BEGLCMHJXHIJLR-UHFFFAOYSA-N methylisothiazolinone Chemical compound CN1SC=CC1=O BEGLCMHJXHIJLR-UHFFFAOYSA-N 0.000 claims description 7
- UZWJYXOTRCVFQE-UHFFFAOYSA-N 1-dodecyl-3-methylpiperidine Chemical compound CCCCCCCCCCCCN1CCCC(C)C1 UZWJYXOTRCVFQE-UHFFFAOYSA-N 0.000 claims description 6
- DITCUBDNORXKGS-UHFFFAOYSA-N 1-dodecyl-4-methylpiperidine Chemical compound CCCCCCCCCCCCN1CCC(C)CC1 DITCUBDNORXKGS-UHFFFAOYSA-N 0.000 claims description 6
- JVCRHTKQAPRUKG-UHFFFAOYSA-N 1-dodecylpyrrolidine Chemical compound CCCCCCCCCCCCN1CCCC1 JVCRHTKQAPRUKG-UHFFFAOYSA-N 0.000 claims description 6
- YFLDZPUXCOSOGU-UHFFFAOYSA-N 1-iodoprop-2-ynyl n-butylcarbamate Chemical compound CCCCNC(=O)OC(I)C#C YFLDZPUXCOSOGU-UHFFFAOYSA-N 0.000 claims description 6
- 229940100555 2-methyl-4-isothiazolin-3-one Drugs 0.000 claims description 6
- NJPQAIBZIHNJDO-UHFFFAOYSA-N 1-dodecylpyrrolidin-2-one Chemical compound CCCCCCCCCCCCN1CCCC1=O NJPQAIBZIHNJDO-UHFFFAOYSA-N 0.000 claims description 5
- 239000000498 cooling water Substances 0.000 claims description 5
- 239000012530 fluid Substances 0.000 claims description 5
- 239000013055 pulp slurry Substances 0.000 claims description 5
- 238000005555 metalworking Methods 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 3
- 239000003599 detergent Substances 0.000 claims description 3
- 125000002632 imidazolidinyl group Chemical group 0.000 claims description 3
- 125000002883 imidazolyl group Chemical group 0.000 claims description 3
- 239000004816 latex Substances 0.000 claims description 3
- 229920000126 latex Polymers 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 125000002757 morpholinyl group Chemical group 0.000 claims description 3
- 125000004193 piperazinyl group Chemical group 0.000 claims description 3
- 125000003386 piperidinyl group Chemical group 0.000 claims description 3
- 125000003072 pyrazolidinyl group Chemical group 0.000 claims description 3
- 125000002755 pyrazolinyl group Chemical group 0.000 claims description 3
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 3
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 3
- 239000011342 resin composition Substances 0.000 claims description 3
- GUSTUIJJPMXTTI-UHFFFAOYSA-N 1-dodecylazepane Chemical compound CCCCCCCCCCCCN1CCCCCC1 GUSTUIJJPMXTTI-UHFFFAOYSA-N 0.000 claims description 2
- SOAKROFTPUDVLZ-UHFFFAOYSA-N 5-(chloromethyl)-3-dodecyl-1,3-oxazolidin-2-one Chemical compound CCCCCCCCCCCCN1CC(CCl)OC1=O SOAKROFTPUDVLZ-UHFFFAOYSA-N 0.000 claims description 2
- SSYUVFKVRKTANJ-UHFFFAOYSA-N 1-dodecyl-2-methylpiperidine Chemical compound CCCCCCCCCCCCN1CCCCC1C SSYUVFKVRKTANJ-UHFFFAOYSA-N 0.000 claims 5
- BHDDSIBLLZQKRF-UHFFFAOYSA-N 1-dodecylpiperidine Chemical compound CCCCCCCCCCCCN1CCCCC1 BHDDSIBLLZQKRF-UHFFFAOYSA-N 0.000 claims 5
- SBUKOHLFHYSZNG-UHFFFAOYSA-N 4-dodecyl-2,6-dimethylmorpholine Chemical compound CCCCCCCCCCCCN1CC(C)OC(C)C1 SBUKOHLFHYSZNG-UHFFFAOYSA-N 0.000 claims 5
- YTIXGBHAPNMOKU-UHFFFAOYSA-N 2-nitropropane-1,3-diol Chemical compound OCC(CO)[N+]([O-])=O YTIXGBHAPNMOKU-UHFFFAOYSA-N 0.000 claims 4
- 125000002636 imidazolinyl group Chemical group 0.000 claims 2
- 206010053759 Growth retardation Diseases 0.000 claims 1
- 239000013011 aqueous formulation Substances 0.000 claims 1
- 150000002466 imines Chemical class 0.000 claims 1
- 230000001629 suppression Effects 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 31
- 238000004519 manufacturing process Methods 0.000 abstract description 8
- 238000000576 coating method Methods 0.000 abstract description 6
- 239000011248 coating agent Substances 0.000 abstract description 3
- 239000000126 substance Substances 0.000 description 33
- 239000000047 product Substances 0.000 description 23
- 230000000813 microbial effect Effects 0.000 description 18
- 230000000694 effects Effects 0.000 description 17
- 239000000123 paper Substances 0.000 description 15
- 239000007788 liquid Substances 0.000 description 14
- 239000000243 solution Substances 0.000 description 12
- 239000003795 chemical substances by application Substances 0.000 description 10
- 238000006731 degradation reaction Methods 0.000 description 8
- 238000000354 decomposition reaction Methods 0.000 description 7
- 239000000725 suspension Substances 0.000 description 7
- WYVVKGNFXHOCQV-UHFFFAOYSA-N 3-iodoprop-2-yn-1-yl butylcarbamate Chemical compound CCCCNC(=O)OCC#CI WYVVKGNFXHOCQV-UHFFFAOYSA-N 0.000 description 6
- 238000012545 processing Methods 0.000 description 6
- 238000005507 spraying Methods 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- UUIVKBHZENILKB-UHFFFAOYSA-N 2,2-dibromo-2-cyanoacetamide Chemical compound NC(=O)C(Br)(Br)C#N UUIVKBHZENILKB-UHFFFAOYSA-N 0.000 description 5
- 229940126062 Compound A Drugs 0.000 description 5
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 5
- 230000003213 activating effect Effects 0.000 description 5
- 229960003168 bronopol Drugs 0.000 description 5
- 239000003973 paint Substances 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 230000015556 catabolic process Effects 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 239000002689 soil Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 235000013311 vegetables Nutrition 0.000 description 4
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- 239000004480 active ingredient Substances 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000001580 bacterial effect Effects 0.000 description 3
- 238000007598 dipping method Methods 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 230000009422 growth inhibiting effect Effects 0.000 description 3
- 238000007074 heterocyclization reaction Methods 0.000 description 3
- 238000007654 immersion Methods 0.000 description 3
- 239000011087 paperboard Substances 0.000 description 3
- 230000002829 reductive effect Effects 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 239000002699 waste material Substances 0.000 description 3
- UEFCKYIRXORTFI-UHFFFAOYSA-N 1,2-thiazolidin-3-one Chemical compound O=C1CCSN1 UEFCKYIRXORTFI-UHFFFAOYSA-N 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 239000003899 bactericide agent Substances 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 238000013401 experimental design Methods 0.000 description 2
- 230000002538 fungal effect Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 230000001965 increasing effect Effects 0.000 description 2
- 230000002147 killing effect Effects 0.000 description 2
- 230000013011 mating Effects 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 239000002351 wastewater Substances 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 229920001817 Agar Polymers 0.000 description 1
- 241000270728 Alligator Species 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 241000270722 Crocodylidae Species 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- 241000255925 Diptera Species 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 241001467460 Myxogastria Species 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 241000270295 Serpentes Species 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 239000012773 agricultural material Substances 0.000 description 1
- 229940037003 alum Drugs 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 230000000843 anti-fungal effect Effects 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 238000003287 bathing Methods 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 239000003124 biologic agent Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000012612 commercial material Substances 0.000 description 1
- 150000001923 cyclic compounds Chemical class 0.000 description 1
- 150000003997 cyclic ketones Chemical class 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000013400 design of experiment Methods 0.000 description 1
- LNNWVNGFPYWNQE-GMIGKAJZSA-N desomorphine Chemical compound C1C2=CC=C(O)C3=C2[C@]24CCN(C)[C@H]1[C@@H]2CCC[C@@H]4O3 LNNWVNGFPYWNQE-GMIGKAJZSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000003050 experimental design method Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000012213 gelatinous substance Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 239000012770 industrial material Substances 0.000 description 1
- 239000008235 industrial water Substances 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- JPMIIZHYYWMHDT-UHFFFAOYSA-N octhilinone Chemical compound CCCCCCCCN1SC=CC1=O JPMIIZHYYWMHDT-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 125000000160 oxazolidinyl group Chemical group 0.000 description 1
- 125000004043 oxo group Chemical group O=* 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000000644 propagated effect Effects 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000008223 sterile water Substances 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 241001300301 uncultured bacterium Species 0.000 description 1
- 238000005406 washing Methods 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
-
- 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
- A01N43/84—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 six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/50—Treatment of water, waste water, or sewage by addition or application of a germicide or by oligodynamic treatment
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2103/00—Nature of the water, waste water, sewage or sludge to be treated
- C02F2103/02—Non-contaminated water, e.g. for industrial water supply
- C02F2103/023—Water in cooling circuits
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/453,001 | 1995-05-30 | ||
| US08/453,001 US6034081A (en) | 1995-05-30 | 1995-05-30 | Potentiation of biocide activity using an N-alkyl heterocyclic compound |
| PCT/US1996/007677 WO1996038043A1 (en) | 1995-05-30 | 1996-05-28 | Potentiation of biocide activity using an n-alkyl heterocyclic compound |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH11506103A true JPH11506103A (ja) | 1999-06-02 |
| JPH11506103A5 JPH11506103A5 (enExample) | 2004-07-22 |
Family
ID=23798832
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8536575A Ceased JPH11506103A (ja) | 1995-05-30 | 1996-05-28 | Ｎ−アルキルヘテロ環化合物を用いた殺菌効果の活性化 |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US6034081A (enExample) |
| EP (1) | EP0857021B1 (enExample) |
| JP (1) | JPH11506103A (enExample) |
| CN (1) | CN1190869A (enExample) |
| AR (1) | AR002134A1 (enExample) |
| AT (1) | ATE247902T1 (enExample) |
| AU (1) | AU5931596A (enExample) |
| BR (1) | BR9608368A (enExample) |
| CA (1) | CA2222864C (enExample) |
| CZ (1) | CZ378097A3 (enExample) |
| DE (1) | DE69629713T2 (enExample) |
| ES (1) | ES2205033T3 (enExample) |
| MX (1) | MX9709354A (enExample) |
| NO (1) | NO975501L (enExample) |
| NZ (1) | NZ309305A (enExample) |
| PT (1) | PT857021E (enExample) |
| SK (1) | SK160897A3 (enExample) |
| WO (1) | WO1996038043A1 (enExample) |
| ZA (1) | ZA964131B (enExample) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005298422A (ja) * | 2004-04-13 | 2005-10-27 | Japan Enviro Chemicals Ltd | 工業用殺菌組成物 |
| WO2008093844A1 (ja) * | 2007-02-01 | 2008-08-07 | Kyodo Yushi Co., Ltd. | 金属加工用油剤及び金属加工方法 |
| JP2016537379A (ja) * | 2013-11-19 | 2016-12-01 | アーチ・ケミカルズ・インコーポレーテッド | 増強された防腐剤 |
| JP2019026695A (ja) * | 2017-07-27 | 2019-02-21 | 第一工業製薬株式会社 | 水素ガスバリア膜用組成物及びこれを用いた水素ガスバリア膜 |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19722858B4 (de) * | 1997-05-23 | 2004-01-29 | Schülke & Mayr GmbH | Zusammensetzungen auf der Basis von Iodpropinyl- und Formaldehyd-Depot-Verbindungen und deren Verwendung als Konservierungsmittel |
| DE19737315C2 (de) * | 1997-08-27 | 2001-05-10 | Herbert Widulle | Verwendung von Substanzgemischen zur Abtötung von Mycobakterien |
| US5929073A (en) * | 1997-09-16 | 1999-07-27 | Buckman Laboratories International, Inc. | Synergistic antimicrobial compositions containing dodecylmorpholine a salt thereof and dodecylamine or a salt thereof |
| US6866906B2 (en) * | 2000-01-26 | 2005-03-15 | International Paper Company | Cut resistant paper and paper articles and method for making same |
| US20030166483A1 (en) * | 2000-04-04 | 2003-09-04 | Michael Heinzel | Use of 3-iodine-2-propinyl-carbamates as antimicrobial active agent |
| IL138771A0 (en) * | 2000-09-28 | 2001-10-31 | Bromine Compounds Ltd | A compacted 2,2-dibromo-3-nitrilopropionamide |
| US20060254736A1 (en) * | 2001-04-11 | 2006-11-16 | Jackson John F | Paper articles exhibiting water resistance and method for making same |
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| US7279071B2 (en) * | 2001-04-11 | 2007-10-09 | International Paper Company | Paper articles exhibiting water resistance and method for making same |
| ATE478195T1 (de) | 2002-09-13 | 2010-09-15 | Int Paper Co | Papier mit verbesserter steifigkeit und fülle und dessen herstellung |
| MX2007000099A (es) * | 2004-07-06 | 2007-04-10 | Int Paper Co | Substratos de papel que contienen un compuesto antimicrobiano asi como metodos para su produccion y uso. |
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| WO2010148156A1 (en) | 2009-06-16 | 2010-12-23 | International Paper Company | Anti-microbial paper substrates useful in wallboard tape applications |
| GB201010374D0 (en) * | 2010-06-21 | 2010-08-04 | Mtp Innovations Ltd | Disinfectant composition |
| EP2594133B1 (en) * | 2011-11-16 | 2014-03-19 | Rohm and Haas Company | Hindered primary chlorinated amine in a latex formulation |
| US9468681B2 (en) | 2013-03-01 | 2016-10-18 | California Institute Of Technology | Targeted nanoparticles |
| US9132097B2 (en) | 2013-03-01 | 2015-09-15 | California Institute Of Technology | Nanoparticles stabilized with nitrophenylboronic acid compositions |
| EP3714903A1 (en) | 2013-03-01 | 2020-09-30 | California Institute of Technology | Nanoparticles stabilized with niitrophenylboronic acid compositions |
| ES2882255T3 (es) | 2015-07-01 | 2021-12-01 | California Inst Of Techn | Sistemas de administración basados en polímeros de ácido múcico catiónicos |
| US20190249360A1 (en) | 2018-02-15 | 2019-08-15 | Buckman Laboratories International, Inc. | Method And System For Tagging Leather Or Hides Treated With Biocide And Identifying Same |
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| US20250040539A1 (en) | 2021-12-17 | 2025-02-06 | Basf Se | Composition comprising an antimicrobial agent and a carboxamide |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3923870A (en) * | 1973-07-11 | 1975-12-02 | Troy Chemical Corp | Urethanes of 1-halogen substituted alkynes |
| US4173643A (en) * | 1973-12-20 | 1979-11-06 | Rohm And Haas Company | Synergistic microbiocidal compositions |
| US5182277A (en) * | 1985-03-04 | 1993-01-26 | Chinoin Gyogyszer Es Vegyeszeti Termekek Gyara R.T. | Fungicides and plant-growth controlling agents |
| DD243632B1 (de) * | 1985-12-02 | 1990-09-05 | Fahlberg List Veb | Mittel zur bekaempfung von phytopathogenen bakterien und pilzen |
| US4661503A (en) * | 1986-06-16 | 1987-04-28 | Nalco Chemical Company | Synergistic biocide of dodecyl guanidine hydrochloride and a mixture of 5-chloro-2-methyl-4-isothiazolin-3-one |
| US4945109A (en) * | 1988-08-24 | 1990-07-31 | Buckman Laboratories International, Inc. | Ester of carbamic acid useful as a microbicide and a preservative |
| US5219875A (en) * | 1990-11-27 | 1993-06-15 | Rohm And Haas Company | Antimicrobial compositions comprising iodopropargyl butylcarbamate and 1,2-benzisothiazolin-3-one and methods of controlling microbes |
| US5250194A (en) * | 1991-02-13 | 1993-10-05 | Buckman Laboratories International, Inc. | N-dodecyl heterocyclic compounds useful as industrial microbicides and preservatives |
| ZA926535B (en) * | 1991-11-07 | 1994-09-30 | Buckman Laboraties Internation | Synergistic combinations of iodopropargyl compounds with 1,2-benzisothiazolin-3-one in controlling fungal and bacterial growth in aqueous fluids |
| DE4217881A1 (de) * | 1992-05-29 | 1993-12-02 | Henkel Kgaa | Antimikrobielle Wirkstoffgemische |
| AU6240294A (en) * | 1993-02-26 | 1994-09-14 | Wesley-Jessen Corporation | Method and composition for disinfecting contact lenses |
| DE4316845A1 (de) * | 1993-05-19 | 1994-11-24 | Bayer Ag | Mikrobizide Mittel |
-
1995
- 1995-05-30 US US08/453,001 patent/US6034081A/en not_active Expired - Lifetime
-
1996
- 1996-05-23 ZA ZA964131A patent/ZA964131B/xx unknown
- 1996-05-28 CZ CZ973780A patent/CZ378097A3/cs unknown
- 1996-05-28 WO PCT/US1996/007677 patent/WO1996038043A1/en not_active Ceased
- 1996-05-28 EP EP96916627A patent/EP0857021B1/en not_active Expired - Lifetime
- 1996-05-28 BR BR9608368A patent/BR9608368A/pt not_active IP Right Cessation
- 1996-05-28 NZ NZ309305A patent/NZ309305A/xx unknown
- 1996-05-28 CN CN96195490A patent/CN1190869A/zh active Pending
- 1996-05-28 PT PT96916627T patent/PT857021E/pt unknown
- 1996-05-28 AU AU59315/96A patent/AU5931596A/en not_active Abandoned
- 1996-05-28 MX MX9709354A patent/MX9709354A/es not_active IP Right Cessation
- 1996-05-28 JP JP8536575A patent/JPH11506103A/ja not_active Ceased
- 1996-05-28 DE DE69629713T patent/DE69629713T2/de not_active Expired - Lifetime
- 1996-05-28 SK SK1608-97A patent/SK160897A3/sk unknown
- 1996-05-28 CA CA002222864A patent/CA2222864C/en not_active Expired - Fee Related
- 1996-05-28 ES ES96916627T patent/ES2205033T3/es not_active Expired - Lifetime
- 1996-05-28 AT AT96916627T patent/ATE247902T1/de active
- 1996-05-29 AR ARP960102779A patent/AR002134A1/es unknown
-
1997
- 1997-11-28 NO NO975501A patent/NO975501L/no not_active Application Discontinuation
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005298422A (ja) * | 2004-04-13 | 2005-10-27 | Japan Enviro Chemicals Ltd | 工業用殺菌組成物 |
| WO2008093844A1 (ja) * | 2007-02-01 | 2008-08-07 | Kyodo Yushi Co., Ltd. | 金属加工用油剤及び金属加工方法 |
| JP2008189714A (ja) * | 2007-02-01 | 2008-08-21 | Kyodo Yushi Co Ltd | 金属加工用油剤及び金属加工方法 |
| US8375755B2 (en) | 2007-02-01 | 2013-02-19 | Kyodo Yushi Co., Ltd. | Metal working fluid composition and metal working method |
| JP2016537379A (ja) * | 2013-11-19 | 2016-12-01 | アーチ・ケミカルズ・インコーポレーテッド | 増強された防腐剤 |
| JP2019026695A (ja) * | 2017-07-27 | 2019-02-21 | 第一工業製薬株式会社 | 水素ガスバリア膜用組成物及びこれを用いた水素ガスバリア膜 |
Also Published As
| Publication number | Publication date |
|---|---|
| AU5931596A (en) | 1996-12-18 |
| CZ378097A3 (cs) | 1998-08-12 |
| SK160897A3 (en) | 1998-07-08 |
| AR002134A1 (es) | 1998-01-07 |
| CA2222864A1 (en) | 1996-12-05 |
| PT857021E (pt) | 2004-01-30 |
| BR9608368A (pt) | 1999-01-05 |
| ES2205033T3 (es) | 2004-05-01 |
| WO1996038043A1 (en) | 1996-12-05 |
| DE69629713T2 (de) | 2004-03-25 |
| US6034081A (en) | 2000-03-07 |
| NZ309305A (en) | 2000-03-27 |
| CA2222864C (en) | 2003-02-11 |
| ZA964131B (en) | 1996-11-27 |
| NO975501D0 (no) | 1997-11-28 |
| NO975501L (no) | 1998-01-30 |
| CN1190869A (zh) | 1998-08-19 |
| EP0857021A1 (en) | 1998-08-12 |
| ATE247902T1 (de) | 2003-09-15 |
| EP0857021B1 (en) | 2003-08-27 |
| DE69629713D1 (de) | 2003-10-02 |
| MX9709354A (es) | 1998-02-28 |
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