NO327214B1 - Belagt bis(2-pyridintiol-1-oksyd)kobbersalt og anvendelse av bestemte forbindelser til belegging av bis(2-pyridintiol-1-oksyd)kobbersalt. - Google Patents
Belagt bis(2-pyridintiol-1-oksyd)kobbersalt og anvendelse av bestemte forbindelser til belegging av bis(2-pyridintiol-1-oksyd)kobbersalt. Download PDFInfo
- Publication number
- NO327214B1 NO327214B1 NO20005794A NO20005794A NO327214B1 NO 327214 B1 NO327214 B1 NO 327214B1 NO 20005794 A NO20005794 A NO 20005794A NO 20005794 A NO20005794 A NO 20005794A NO 327214 B1 NO327214 B1 NO 327214B1
- Authority
- NO
- Norway
- Prior art keywords
- oxide
- bis
- pyridinethiol
- copper salt
- weight
- Prior art date
Links
- 150000001879 copper Chemical class 0.000 title claims description 130
- YBBJKCMMCRQZMA-UHFFFAOYSA-N pyrithione Chemical compound ON1C=CC=CC1=S YBBJKCMMCRQZMA-UHFFFAOYSA-N 0.000 title claims description 124
- 239000011248 coating agent Substances 0.000 title claims description 39
- 238000000576 coating method Methods 0.000 title claims description 32
- 150000001875 compounds Chemical class 0.000 title claims description 30
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 40
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims description 26
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 claims description 26
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 claims description 26
- 235000011187 glycerol Nutrition 0.000 claims description 20
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 19
- 229930195729 fatty acid Natural products 0.000 claims description 19
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- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 claims description 13
- 239000005077 polysulfide Substances 0.000 claims description 13
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- 229940099259 vaseline Drugs 0.000 claims description 5
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- 239000000203 mixture Substances 0.000 description 13
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 12
- 230000003373 anti-fouling effect Effects 0.000 description 12
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 12
- 229910052749 magnesium Inorganic materials 0.000 description 12
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- 239000011777 magnesium Substances 0.000 description 12
- 229940091250 magnesium supplement Drugs 0.000 description 12
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 11
- 229910052802 copper Inorganic materials 0.000 description 11
- 239000010949 copper Substances 0.000 description 11
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 10
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- 150000003839 salts Chemical class 0.000 description 7
- 230000001681 protective effect Effects 0.000 description 6
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- 125000000217 alkyl group Chemical group 0.000 description 3
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- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 3
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- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- WWJCRUKUIQRCGP-UHFFFAOYSA-N 3-(dimethylamino)propyl 2-methylprop-2-enoate Chemical compound CN(C)CCCOC(=O)C(C)=C WWJCRUKUIQRCGP-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
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- DQEDNTOLSZERJI-UHFFFAOYSA-N C(C=C)(=O)O.C(CCCCCCCCCCCCCCC(C)C)(=O)O Chemical compound C(C=C)(=O)O.C(CCCCCCCCCCCCCCC(C)C)(=O)O DQEDNTOLSZERJI-UHFFFAOYSA-N 0.000 description 2
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 2
- 239000005751 Copper oxide Substances 0.000 description 2
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- 230000000052 comparative effect Effects 0.000 description 2
- 229910000431 copper oxide Inorganic materials 0.000 description 2
- VZWHXRLOECMQDD-UHFFFAOYSA-L copper;2-methylprop-2-enoate Chemical compound [Cu+2].CC(=C)C([O-])=O.CC(=C)C([O-])=O VZWHXRLOECMQDD-UHFFFAOYSA-L 0.000 description 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- JQCXWCOOWVGKMT-UHFFFAOYSA-N diheptyl phthalate Chemical compound CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC JQCXWCOOWVGKMT-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
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- DWLAVVBOGOXHNH-UHFFFAOYSA-L magnesium;prop-2-enoate Chemical compound [Mg+2].[O-]C(=O)C=C.[O-]C(=O)C=C DWLAVVBOGOXHNH-UHFFFAOYSA-L 0.000 description 1
- JTASLOIQRBWGBY-UHFFFAOYSA-L magnesium;prop-2-enoate;2-(2,4,5-trichlorophenoxy)acetate Chemical compound [Mg+2].[O-]C(=O)C=C.[O-]C(=O)COC1=CC(Cl)=C(Cl)C=C1Cl JTASLOIQRBWGBY-UHFFFAOYSA-L 0.000 description 1
- LYMCSKWJSAMLTC-UHFFFAOYSA-L magnesium;prop-2-enoate;quinoline-2-carboxylate Chemical compound [Mg+2].[O-]C(=O)C=C.C1=CC=CC2=NC(C(=O)[O-])=CC=C21 LYMCSKWJSAMLTC-UHFFFAOYSA-L 0.000 description 1
- AUDWHSOEPRVTSE-UHFFFAOYSA-L magnesium;propanoate;prop-2-enoate Chemical compound [Mg+2].CCC([O-])=O.[O-]C(=O)C=C AUDWHSOEPRVTSE-UHFFFAOYSA-L 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- FTQWRYSLUYAIRQ-UHFFFAOYSA-N n-[(octadecanoylamino)methyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCNC(=O)CCCCCCCCCCCCCCCCC FTQWRYSLUYAIRQ-UHFFFAOYSA-N 0.000 description 1
- RKISUIUJZGSLEV-UHFFFAOYSA-N n-[2-(octadecanoylamino)ethyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCNC(=O)CCCCCCCCCCCCCCCCC RKISUIUJZGSLEV-UHFFFAOYSA-N 0.000 description 1
- RCLLINSDAJVOHP-UHFFFAOYSA-N n-ethyl-n',n'-dimethylprop-2-enehydrazide Chemical compound CCN(N(C)C)C(=O)C=C RCLLINSDAJVOHP-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 125000001196 nonadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 210000001331 nose Anatomy 0.000 description 1
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- QIWKUEJZZCOPFV-UHFFFAOYSA-N phenyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1=CC=CC=C1 QIWKUEJZZCOPFV-UHFFFAOYSA-N 0.000 description 1
- WRAQQYDMVSCOTE-UHFFFAOYSA-N phenyl prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1 WRAQQYDMVSCOTE-UHFFFAOYSA-N 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 229960002026 pyrithione Drugs 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 229940037312 stearamide Drugs 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- SJMYWORNLPSJQO-UHFFFAOYSA-N tert-butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)(C)C SJMYWORNLPSJQO-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 210000003437 trachea Anatomy 0.000 description 1
- WEAZWKYSTGLBSQ-UHFFFAOYSA-N tributylsilyl 2-methylprop-2-enoate Chemical compound CCCC[Si](CCCC)(CCCC)OC(=O)C(C)=C WEAZWKYSTGLBSQ-UHFFFAOYSA-N 0.000 description 1
- PWVJTRQTFFVDEU-UHFFFAOYSA-N triethylsilyl 2-methylprop-2-enoate Chemical compound CC[Si](CC)(CC)OC(=O)C(C)=C PWVJTRQTFFVDEU-UHFFFAOYSA-N 0.000 description 1
- UGKLJUIMKCCNGS-UHFFFAOYSA-N triethylsilyl prop-2-enoate Chemical compound CC[Si](CC)(CC)OC(=O)C=C UGKLJUIMKCCNGS-UHFFFAOYSA-N 0.000 description 1
- PGQNYIRJCLTTOJ-UHFFFAOYSA-N trimethylsilyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)O[Si](C)(C)C PGQNYIRJCLTTOJ-UHFFFAOYSA-N 0.000 description 1
- OTYBJBJYBGWBHB-UHFFFAOYSA-N trimethylsilyl prop-2-enoate Chemical compound C[Si](C)(C)OC(=O)C=C OTYBJBJYBGWBHB-UHFFFAOYSA-N 0.000 description 1
- PIQIWPDMOYYEBV-UHFFFAOYSA-N triphenylsilyl 2-methylprop-2-enoate Chemical compound C=1C=CC=CC=1[Si](C=1C=CC=CC=1)(OC(=O)C(=C)C)C1=CC=CC=C1 PIQIWPDMOYYEBV-UHFFFAOYSA-N 0.000 description 1
- HVMNIRCQQXUXRP-UHFFFAOYSA-N triphenylsilyl prop-2-enoate Chemical compound C=1C=CC=CC=1[Si](C=1C=CC=CC=1)(OC(=O)C=C)C1=CC=CC=C1 HVMNIRCQQXUXRP-UHFFFAOYSA-N 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000003871 white petrolatum Substances 0.000 description 1
- LPFHHWSLGUURSL-UHFFFAOYSA-L zinc;2-(2,4-dichlorophenoxy)acetate;2-methylprop-2-enoate Chemical compound [Zn+2].CC(=C)C([O-])=O.[O-]C(=O)COC1=CC=C(Cl)C=C1Cl LPFHHWSLGUURSL-UHFFFAOYSA-L 0.000 description 1
- XYRHHIXXSKVANY-UHFFFAOYSA-L zinc;2-(2,4-dichlorophenoxy)acetate;prop-2-enoate Chemical compound [Zn+2].[O-]C(=O)C=C.[O-]C(=O)COC1=CC=C(Cl)C=C1Cl XYRHHIXXSKVANY-UHFFFAOYSA-L 0.000 description 1
- KORODMGBDFGXAC-UHFFFAOYSA-L zinc;2-chloroacetate;2-methylprop-2-enoate Chemical compound [Zn+2].[O-]C(=O)CCl.CC(=C)C([O-])=O KORODMGBDFGXAC-UHFFFAOYSA-L 0.000 description 1
- OBKMKSCKZFYWGM-UHFFFAOYSA-L zinc;2-fluoroacetate;2-methylprop-2-enoate Chemical compound [Zn+2].[O-]C(=O)CF.CC(=C)C([O-])=O OBKMKSCKZFYWGM-UHFFFAOYSA-L 0.000 description 1
- QFKPGWUCDIBVDH-UHFFFAOYSA-L zinc;2-methylprop-2-enoate;2-(2,4,5-trichlorophenoxy)acetate Chemical compound [Zn+2].CC(=C)C([O-])=O.[O-]C(=O)COC1=CC(Cl)=C(Cl)C=C1Cl QFKPGWUCDIBVDH-UHFFFAOYSA-L 0.000 description 1
- FOFDIQWJSAXLJW-UHFFFAOYSA-L zinc;2-methylprop-2-enoate;2-nitrobenzoate Chemical compound [Zn+2].CC(=C)C([O-])=O.[O-]C(=O)C1=CC=CC=C1[N+]([O-])=O FOFDIQWJSAXLJW-UHFFFAOYSA-L 0.000 description 1
- GXVKJKLXRSGSDH-UHFFFAOYSA-L zinc;2-methylprop-2-enoate;2-nitronaphthalene-1-carboxylate Chemical compound [Zn+2].CC(=C)C([O-])=O.C1=CC=C2C(C(=O)[O-])=C([N+]([O-])=O)C=CC2=C1 GXVKJKLXRSGSDH-UHFFFAOYSA-L 0.000 description 1
- NDOZRESYLDMABN-UHFFFAOYSA-L zinc;2-methylprop-2-enoate;benzoate Chemical compound [Zn+2].CC(=C)C([O-])=O.[O-]C(=O)C1=CC=CC=C1 NDOZRESYLDMABN-UHFFFAOYSA-L 0.000 description 1
- KAFGAFXGBNCRKR-UHFFFAOYSA-L zinc;2-methylprop-2-enoate;octadecanoate Chemical compound [Zn+2].CC(=C)C([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O KAFGAFXGBNCRKR-UHFFFAOYSA-L 0.000 description 1
- MCFVXOZZCZYQNL-UHFFFAOYSA-L zinc;2-methylprop-2-enoate;octanoate Chemical compound [Zn+2].CC(=C)C([O-])=O.CCCCCCCC([O-])=O MCFVXOZZCZYQNL-UHFFFAOYSA-L 0.000 description 1
- WOQSHHHKBNWSCM-UHFFFAOYSA-L zinc;2-methylprop-2-enoate;propanoate Chemical compound [Zn+2].CCC([O-])=O.CC(=C)C([O-])=O WOQSHHHKBNWSCM-UHFFFAOYSA-L 0.000 description 1
- BYXRFDOXKPAPQI-UHFFFAOYSA-L zinc;2-methylprop-2-enoate;quinoline-2-carboxylate Chemical compound [Zn+2].CC(=C)C([O-])=O.C1=CC=CC2=NC(C(=O)[O-])=CC=C21 BYXRFDOXKPAPQI-UHFFFAOYSA-L 0.000 description 1
- KHUWTSBHJCVGRK-UHFFFAOYSA-L zinc;2-nitrobenzoate;prop-2-enoate Chemical compound [Zn+2].[O-]C(=O)C=C.[O-]C(=O)C1=CC=CC=C1[N+]([O-])=O KHUWTSBHJCVGRK-UHFFFAOYSA-L 0.000 description 1
- BQHUBQCESSWXPD-UHFFFAOYSA-L zinc;2-nitronaphthalene-1-carboxylate;prop-2-enoate Chemical compound [Zn+2].[O-]C(=O)C=C.C1=CC=C2C(C(=O)[O-])=C([N+]([O-])=O)C=CC2=C1 BQHUBQCESSWXPD-UHFFFAOYSA-L 0.000 description 1
- TVJVCOFLTUEESM-UHFFFAOYSA-L zinc;hexadecanoate;2-methylprop-2-enoate Chemical compound [Zn+2].CC(=C)C([O-])=O.CCCCCCCCCCCCCCCC([O-])=O TVJVCOFLTUEESM-UHFFFAOYSA-L 0.000 description 1
- CTZRTRJVDZZEGT-UHFFFAOYSA-L zinc;hexadecanoate;prop-2-enoate Chemical compound [Zn+2].[O-]C(=O)C=C.CCCCCCCCCCCCCCCC([O-])=O CTZRTRJVDZZEGT-UHFFFAOYSA-L 0.000 description 1
- XXCQLLQHTFLKPE-UHFFFAOYSA-L zinc;octadecanoate;prop-2-enoate Chemical compound [Zn+2].[O-]C(=O)C=C.CCCCCCCCCCCCCCCCCC([O-])=O XXCQLLQHTFLKPE-UHFFFAOYSA-L 0.000 description 1
- DZIWJJRNBIIMAP-UHFFFAOYSA-L zinc;octanoate;prop-2-enoate Chemical compound [Zn+2].[O-]C(=O)C=C.CCCCCCCC([O-])=O DZIWJJRNBIIMAP-UHFFFAOYSA-L 0.000 description 1
- XKMZOFXGLBYJLS-UHFFFAOYSA-L zinc;prop-2-enoate Chemical compound [Zn+2].[O-]C(=O)C=C.[O-]C(=O)C=C XKMZOFXGLBYJLS-UHFFFAOYSA-L 0.000 description 1
- XQELUZYQAMHELT-UHFFFAOYSA-L zinc;prop-2-enoate;2-(2,4,5-trichlorophenoxy)acetate Chemical compound [Zn+2].[O-]C(=O)C=C.[O-]C(=O)COC1=CC(Cl)=C(Cl)C=C1Cl XQELUZYQAMHELT-UHFFFAOYSA-L 0.000 description 1
- GXTFJSCLUPBSCT-UHFFFAOYSA-L zinc;prop-2-enoate;benzoate Chemical compound [Zn+2].[O-]C(=O)C=C.[O-]C(=O)C1=CC=CC=C1 GXTFJSCLUPBSCT-UHFFFAOYSA-L 0.000 description 1
- ZMMDDNWOALVYRP-UHFFFAOYSA-L zinc;prop-2-enoate;quinoline-2-carboxylate Chemical compound [Zn+2].[O-]C(=O)C=C.C1=CC=CC2=NC(C(=O)[O-])=CC=C21 ZMMDDNWOALVYRP-UHFFFAOYSA-L 0.000 description 1
- KJROUBUHARNBCN-UHFFFAOYSA-L zinc;propanoate;prop-2-enoate Chemical compound [Zn+2].CCC([O-])=O.[O-]C(=O)C=C KJROUBUHARNBCN-UHFFFAOYSA-L 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Paints Or Removers (AREA)
- Medicinal Preparation (AREA)
- Pyridine Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7272799 | 1999-03-17 | ||
JP11295799 | 1999-04-20 | ||
JP11295899 | 1999-04-20 | ||
PCT/JP2000/001638 WO2000054589A1 (fr) | 1999-03-17 | 2000-03-17 | Sel de cuivre bis (2-pyridinethiol 1-oxyde) enrobe |
Publications (3)
Publication Number | Publication Date |
---|---|
NO20005794D0 NO20005794D0 (no) | 2000-11-16 |
NO20005794L NO20005794L (no) | 2000-12-14 |
NO327214B1 true NO327214B1 (no) | 2009-05-11 |
Family
ID=27301019
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20005794A NO327214B1 (no) | 1999-03-17 | 2000-11-16 | Belagt bis(2-pyridintiol-1-oksyd)kobbersalt og anvendelse av bestemte forbindelser til belegging av bis(2-pyridintiol-1-oksyd)kobbersalt. |
Country Status (9)
Country | Link |
---|---|
US (2) | US6544440B1 (de) |
EP (1) | EP1080640B1 (de) |
JP (1) | JP4815669B2 (de) |
KR (1) | KR100679497B1 (de) |
CN (1) | CN1159965C (de) |
AT (1) | ATE249142T1 (de) |
DE (1) | DE60005101D1 (de) |
NO (1) | NO327214B1 (de) |
WO (1) | WO2000054589A1 (de) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6627665B2 (en) * | 2001-09-28 | 2003-09-30 | Arch Chemicals, Inc. | Non-dusting copper pyrithione dispersion |
US7481873B2 (en) | 2002-12-20 | 2009-01-27 | Arch Chemicals, Inc. | Small particle copper pyrithione |
US6821326B2 (en) * | 2002-12-20 | 2004-11-23 | Arch Chemicals, Inc. | Small particle copper pyrithione |
JP4629311B2 (ja) * | 2003-01-21 | 2011-02-09 | 株式会社エーピーアイ コーポレーション | 金属ピリチオンの油性分散組成物 |
US8980235B2 (en) * | 2003-09-30 | 2015-03-17 | Arch Chemicals, Inc. | Coated metal pyrithione particles for treatment of microorganisms |
KR100529159B1 (ko) * | 2005-02-22 | 2005-11-17 | 주식회사 코오롱 | 특정 입도 분포를 갖는 피리치온 금속염 및 이를 포함하는도료 조성물 |
US7893047B2 (en) | 2006-03-03 | 2011-02-22 | Arch Chemicals, Inc. | Biocide composition comprising pyrithione and pyrrole derivatives |
US10064273B2 (en) | 2015-10-20 | 2018-08-28 | MR Label Company | Antimicrobial copper sheet overlays and related methods for making and using |
Family Cites Families (29)
Publication number | Priority date | Publication date | Assignee | Title |
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JPS5323383B2 (de) * | 1972-01-14 | 1978-07-14 | ||
JPS5537521B2 (de) * | 1973-09-22 | 1980-09-29 | ||
JPS5327630A (en) * | 1976-08-27 | 1978-03-15 | Hokko Chem Ind Co Ltd | Underwater antifouling coating compounds |
JPS5478733A (en) * | 1977-12-06 | 1979-06-23 | Hokko Chem Ind Co Ltd | Underwater antifouling coating compound |
JPS5415939A (en) * | 1978-07-01 | 1979-02-06 | Hokko Chem Ind Co Ltd | Underwater antifouling coating compound |
JPS5536221A (en) * | 1978-09-05 | 1980-03-13 | Hokko Chem Ind Co Ltd | Underwater antifouling coating material |
JPS5659701A (en) * | 1980-01-30 | 1981-05-23 | Nippon Nohyaku Co Ltd | Powdery agricultural chemical composition containing little dust and its preparation |
JPS57158707A (en) * | 1981-03-26 | 1982-09-30 | Hokko Chem Ind Co Ltd | Improved powdery pesticide |
JPS57159701A (en) * | 1981-03-27 | 1982-10-01 | Hokko Chem Ind Co Ltd | Improved dust of agricultural chemical |
US4474760A (en) * | 1983-06-22 | 1984-10-02 | Excalibur, Inc. | Stabilized 2-mercaptopyridene-1-oxide and derivatives |
JP2886572B2 (ja) * | 1989-10-03 | 1999-04-26 | 三共株式会社 | 農薬粒剤の製造方法 |
US5057153A (en) * | 1990-05-03 | 1991-10-15 | Olin Corporation | Paint containing high levels of a pyrithione salt plus a copper salt |
JP2696188B2 (ja) * | 1992-07-08 | 1998-01-14 | 大日本製薬株式会社 | 防汚塗料組成物 |
JPH06100405A (ja) * | 1992-08-07 | 1994-04-12 | Yoshitomi Pharmaceut Ind Ltd | 水中防汚剤 |
US5185033A (en) * | 1992-09-01 | 1993-02-09 | Olin Corporation | Gel-free paint containing copper pyrithione or pyrithione disulfide plus cuprous oxide |
US5238490A (en) * | 1992-09-04 | 1993-08-24 | Olin Corporation | Process for generating copper pyrithione in-situ in a paint formulation |
JPH0789818A (ja) * | 1993-09-17 | 1995-04-04 | Sintokogio Ltd | 砂場に抗菌性を付与する方法 |
JP3120201B2 (ja) | 1994-02-25 | 2000-12-25 | セイコー精機株式会社 | 加工装置のチャック装置 |
EP0679333A3 (de) | 1994-04-28 | 1996-01-03 | Rohm & Haas | Nicht sensiblisierende biozide Zusammensetzung. |
US5476833A (en) | 1994-05-13 | 1995-12-19 | Fersch; Kenneth E. | Water dispersible agricultural chemical granules coated with thin PVA film to reduce/eliminate container residue |
JP3451786B2 (ja) * | 1995-03-29 | 2003-09-29 | 日本油脂Basfコーティングス株式会社 | 塗料組成物 |
JPH09273075A (ja) * | 1996-04-01 | 1997-10-21 | Toyobo Co Ltd | 生物抵抗性を有する繊維の製造方法 |
SG60054A1 (en) * | 1996-04-17 | 1999-02-22 | Nof Corp | Coating composition |
JPH10130685A (ja) * | 1996-10-30 | 1998-05-19 | Daikin Ind Ltd | 冷凍装置 |
JPH10298455A (ja) | 1997-04-23 | 1998-11-10 | Nippon Paint Co Ltd | 防汚塗料組成物 |
JPH1129402A (ja) * | 1997-05-15 | 1999-02-02 | Yoshitomi Fine Chem Kk | 水性抗菌剤分散液 |
JP2000001410A (ja) * | 1998-04-17 | 2000-01-07 | Nissan Chem Ind Ltd | 海中生物付着防止組成物及び該組成物を含む防汚塗料 |
JP2000026649A (ja) * | 1998-07-15 | 2000-01-25 | Achilles Corp | 防藻性発泡性樹脂粒子及びその成形体 |
JP2000072989A (ja) * | 1998-08-31 | 2000-03-07 | Yoshitomi Fine Chemical Kk | 水中防汚塗料 |
-
2000
- 2000-03-17 JP JP2000604683A patent/JP4815669B2/ja not_active Expired - Fee Related
- 2000-03-17 DE DE60005101T patent/DE60005101D1/de not_active Expired - Lifetime
- 2000-03-17 KR KR1020007012885A patent/KR100679497B1/ko not_active IP Right Cessation
- 2000-03-17 US US09/700,648 patent/US6544440B1/en not_active Expired - Fee Related
- 2000-03-17 CN CNB008003491A patent/CN1159965C/zh not_active Expired - Fee Related
- 2000-03-17 AT AT00909705T patent/ATE249142T1/de not_active IP Right Cessation
- 2000-03-17 WO PCT/JP2000/001638 patent/WO2000054589A1/ja active IP Right Grant
- 2000-03-17 EP EP00909705A patent/EP1080640B1/de not_active Expired - Lifetime
- 2000-11-16 NO NO20005794A patent/NO327214B1/no not_active IP Right Cessation
-
2003
- 2003-01-08 US US10/337,844 patent/US6630079B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
DE60005101D1 (de) | 2003-10-16 |
KR20010043679A (ko) | 2001-05-25 |
US6544440B1 (en) | 2003-04-08 |
US20030124085A1 (en) | 2003-07-03 |
KR100679497B1 (ko) | 2007-02-07 |
EP1080640B1 (de) | 2003-09-10 |
US6630079B2 (en) | 2003-10-07 |
NO20005794D0 (no) | 2000-11-16 |
CN1296380A (zh) | 2001-05-23 |
JP4815669B2 (ja) | 2011-11-16 |
EP1080640A1 (de) | 2001-03-07 |
WO2000054589A1 (fr) | 2000-09-21 |
ATE249142T1 (de) | 2003-09-15 |
NO20005794L (no) | 2000-12-14 |
CN1159965C (zh) | 2004-08-04 |
EP1080640A4 (de) | 2002-03-20 |
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