DK2632267T3 - Svampedræbende penflufen-blandinger - Google Patents
Svampedræbende penflufen-blandinger Download PDFInfo
- Publication number
- DK2632267T3 DK2632267T3 DK11764728.9T DK11764728T DK2632267T3 DK 2632267 T3 DK2632267 T3 DK 2632267T3 DK 11764728 T DK11764728 T DK 11764728T DK 2632267 T3 DK2632267 T3 DK 2632267T3
- Authority
- DK
- Denmark
- Prior art keywords
- compounds
- wood
- propynyl
- iodo
- formula
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 61
- GOFJDXZZHFNFLV-UHFFFAOYSA-N 5-fluoro-1,3-dimethyl-N-[2-(4-methylpentan-2-yl)phenyl]pyrazole-4-carboxamide Chemical compound CC(C)CC(C)C1=CC=CC=C1NC(=O)C1=C(F)N(C)N=C1C GOFJDXZZHFNFLV-UHFFFAOYSA-N 0.000 title claims description 45
- 239000005815 Penflufen Substances 0.000 title claims description 45
- 230000000855 fungicidal effect Effects 0.000 title description 4
- -1 alkaline earth metal salts Chemical class 0.000 claims description 156
- 150000001875 compounds Chemical class 0.000 claims description 68
- 239000002023 wood Substances 0.000 claims description 34
- 239000002253 acid Substances 0.000 claims description 31
- 150000003839 salts Chemical class 0.000 claims description 24
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 claims description 23
- 239000012770 industrial material Substances 0.000 claims description 18
- WYVVKGNFXHOCQV-UHFFFAOYSA-N 3-iodoprop-2-yn-1-yl butylcarbamate Chemical compound CCCCNC(=O)OCC#CI WYVVKGNFXHOCQV-UHFFFAOYSA-N 0.000 claims description 17
- 244000005700 microbiome Species 0.000 claims description 15
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 13
- 229910052783 alkali metal Inorganic materials 0.000 claims description 12
- CXIVKQSIEXBSRQ-UHFFFAOYSA-N 4,5-dichloro-2-octyl-1,2-thiazolidin-3-one Chemical compound CCCCCCCCN1SC(Cl)C(Cl)C1=O CXIVKQSIEXBSRQ-UHFFFAOYSA-N 0.000 claims description 11
- 150000001340 alkali metals Chemical class 0.000 claims description 11
- 229910021538 borax Inorganic materials 0.000 claims description 11
- 150000001639 boron compounds Chemical class 0.000 claims description 11
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 claims description 11
- TXOJCSIIFFMREV-UHFFFAOYSA-L didecyl(dimethyl)azanium;carbonate Chemical compound [O-]C([O-])=O.CCCCCCCCCC[N+](C)(C)CCCCCCCCCC.CCCCCCCCCC[N+](C)(C)CCCCCCCCCC TXOJCSIIFFMREV-UHFFFAOYSA-L 0.000 claims description 11
- 235000010292 orthophenyl phenol Nutrition 0.000 claims description 11
- 235000010339 sodium tetraborate Nutrition 0.000 claims description 11
- VUWCWMOCWKCZTA-UHFFFAOYSA-N 1,2-thiazol-4-one Chemical class O=C1CSN=C1 VUWCWMOCWKCZTA-UHFFFAOYSA-N 0.000 claims description 10
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 10
- RUPBZQFQVRMKDG-UHFFFAOYSA-M Didecyldimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCC[N+](C)(C)CCCCCCCCCC RUPBZQFQVRMKDG-UHFFFAOYSA-M 0.000 claims description 9
- 229920001587 Wood-plastic composite Polymers 0.000 claims description 9
- 239000004327 boric acid Substances 0.000 claims description 9
- 229960004670 didecyldimethylammonium chloride Drugs 0.000 claims description 9
- 239000011155 wood-plastic composite Substances 0.000 claims description 9
- 229960000686 benzalkonium chloride Drugs 0.000 claims description 8
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 claims description 8
- 229910052810 boron oxide Inorganic materials 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- XJMWHXZUIGHOBA-UHFFFAOYSA-N azane;propanoic acid Chemical compound N.CCC(O)=O XJMWHXZUIGHOBA-UHFFFAOYSA-N 0.000 claims description 7
- MVTVVKOMNZGDGD-UHFFFAOYSA-M didecyl(dimethyl)azanium;hydron;carbonate Chemical compound OC([O-])=O.CCCCCCCCCC[N+](C)(C)CCCCCCCCCC MVTVVKOMNZGDGD-UHFFFAOYSA-M 0.000 claims description 7
- NYNKJVPRTLBJNQ-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-dodecylpropane-1,3-diamine Chemical compound CCCCCCCCCCCCN(CCCN)CCCN NYNKJVPRTLBJNQ-UHFFFAOYSA-N 0.000 claims description 7
- 241000894007 species Species 0.000 claims description 7
- 125000003342 alkenyl group Chemical group 0.000 claims description 6
- 150000001450 anions Chemical class 0.000 claims description 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 6
- 239000004328 sodium tetraborate Substances 0.000 claims description 6
- 230000006378 damage Effects 0.000 claims description 5
- 125000006286 dichlorobenzyl group Chemical group 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- AVGVFDSUDIUXEU-UHFFFAOYSA-N 2-octyl-1,2-thiazolidin-3-one Chemical compound CCCCCCCCN1SCCC1=O AVGVFDSUDIUXEU-UHFFFAOYSA-N 0.000 claims description 4
- CIOQSQQVHVGYHS-UHFFFAOYSA-N 5-chloro-2-octyl-1,2-thiazolidin-4-one Chemical compound CCCCCCCCN1CC(=O)C(Cl)S1 CIOQSQQVHVGYHS-UHFFFAOYSA-N 0.000 claims description 4
- 241000221198 Basidiomycota Species 0.000 claims description 4
- MAUSFGZARPIQOD-UHFFFAOYSA-N S1NC=CC2=C1C=CC2=O Chemical compound S1NC=CC2=C1C=CC2=O MAUSFGZARPIQOD-UHFFFAOYSA-N 0.000 claims description 4
- DHNRXBZYEKSXIM-UHFFFAOYSA-N chloromethylisothiazolinone Chemical compound CN1SC(Cl)=CC1=O DHNRXBZYEKSXIM-UHFFFAOYSA-N 0.000 claims description 4
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 claims description 4
- 241001600093 Coniophora Species 0.000 claims description 3
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- HKEBWESLPJXKAA-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-decylpropane-1,3-diamine Chemical compound CCCCCCCCCCN(CCCN)CCCN HKEBWESLPJXKAA-UHFFFAOYSA-N 0.000 claims description 3
- FKLAQMPTKFHTBS-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-tetradecylpropane-1,3-diamine Chemical compound CCCCCCCCCCCCCCN(CCCN)CCCN FKLAQMPTKFHTBS-UHFFFAOYSA-N 0.000 claims description 3
- 241000222356 Coriolus Species 0.000 claims description 2
- 241000123332 Gloeophyllum Species 0.000 claims description 2
- 241001619461 Poria <basidiomycete fungus> Species 0.000 claims description 2
- 241000222646 Stereum Species 0.000 claims description 2
- MGIYRDNGCNKGJU-UHFFFAOYSA-N isothiazolinone Chemical compound O=C1C=CSN1 MGIYRDNGCNKGJU-UHFFFAOYSA-N 0.000 claims description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
- YEJOKPFEBPJVMQ-UHFFFAOYSA-N 2-ethylpent-3-ynylcarbamic acid Chemical compound CC#CC(CC)CNC(O)=O YEJOKPFEBPJVMQ-UHFFFAOYSA-N 0.000 claims 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims 1
- 229910052796 boron Inorganic materials 0.000 claims 1
- 150000004691 decahydrates Chemical class 0.000 claims 1
- RDMZIKMKSGCBKK-UHFFFAOYSA-N disodium;(9,11-dioxido-5-oxoboranyloxy-2,4,6,8,10,12,13-heptaoxa-1,3,5,7,9,11-hexaborabicyclo[5.5.1]tridecan-3-yl)oxy-oxoborane;tetrahydrate Chemical compound O.O.O.O.[Na+].[Na+].O1B(OB=O)OB(OB=O)OB2OB([O-])OB([O-])OB1O2 RDMZIKMKSGCBKK-UHFFFAOYSA-N 0.000 claims 1
- AJFXNBUVIBKWBT-UHFFFAOYSA-N disodium;boric acid;hydrogen borate Chemical compound [Na+].[Na+].OB(O)O.OB(O)O.OB(O)O.OB([O-])[O-] AJFXNBUVIBKWBT-UHFFFAOYSA-N 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 239000011630 iodine Substances 0.000 claims 1
- BEGLCMHJXHIJLR-UHFFFAOYSA-N methylisothiazolinone Chemical compound CN1SC=CC1=O BEGLCMHJXHIJLR-UHFFFAOYSA-N 0.000 claims 1
- 239000000463 material Substances 0.000 description 10
- 239000002131 composite material Substances 0.000 description 9
- 241001492489 Postia placenta Species 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 230000002195 synergetic effect Effects 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- 239000010949 copper Substances 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 238000009472 formulation Methods 0.000 description 6
- 239000003292 glue Substances 0.000 description 6
- 229920003023 plastic Polymers 0.000 description 6
- 239000004033 plastic Substances 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- 241000233866 Fungi Species 0.000 description 5
- 241000222355 Trametes versicolor Species 0.000 description 5
- 150000003857 carboxamides Chemical class 0.000 description 5
- 229910052802 copper Inorganic materials 0.000 description 5
- 239000008187 granular material Substances 0.000 description 5
- 239000002917 insecticide Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 150000003254 radicals Chemical class 0.000 description 5
- 229910052725 zinc Inorganic materials 0.000 description 5
- 239000011701 zinc Substances 0.000 description 5
- PORQOHRXAJJKGK-UHFFFAOYSA-N 4,5-dichloro-2-n-octyl-3(2H)-isothiazolone Chemical compound CCCCCCCCN1SC(Cl)=C(Cl)C1=O PORQOHRXAJJKGK-UHFFFAOYSA-N 0.000 description 4
- 241001492300 Gloeophyllum trabeum Species 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000417 fungicide Substances 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000011135 tin Substances 0.000 description 4
- 229910052718 tin Inorganic materials 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- SJXPQSRCFCPWQQ-UHFFFAOYSA-N 2-methyl-1,2-thiazol-2-ium-3-ol;chloride Chemical compound Cl.CN1SC=CC1=O SJXPQSRCFCPWQQ-UHFFFAOYSA-N 0.000 description 3
- 125000003852 3-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(Cl)=C1[H])C([H])([H])* 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 3
- JMHWNJGXUIJPKG-UHFFFAOYSA-N CC(=O)O[SiH](CC=C)OC(C)=O Chemical compound CC(=O)O[SiH](CC=C)OC(C)=O JMHWNJGXUIJPKG-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 239000004606 Fillers/Extenders Substances 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 241001425746 Stereum sanguinolentum Species 0.000 description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 230000000844 anti-bacterial effect Effects 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000003899 bactericide agent Substances 0.000 description 3
- JBIROUFYLSSYDX-UHFFFAOYSA-M benzododecinium chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 JBIROUFYLSSYDX-UHFFFAOYSA-M 0.000 description 3
- OCBHHZMJRVXXQK-UHFFFAOYSA-M benzyl-dimethyl-tetradecylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 OCBHHZMJRVXXQK-UHFFFAOYSA-M 0.000 description 3
- WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 3
- 239000011093 chipboard Substances 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Aalpha Natural products C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 230000000813 microbial effect Effects 0.000 description 3
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 239000011120 plywood Substances 0.000 description 3
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 3
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- KRQUFUKTQHISJB-YYADALCUSA-N 2-[(E)-N-[2-(4-chlorophenoxy)propoxy]-C-propylcarbonimidoyl]-3-hydroxy-5-(thian-3-yl)cyclohex-2-en-1-one Chemical compound CCC\C(=N/OCC(C)OC1=CC=C(Cl)C=C1)C1=C(O)CC(CC1=O)C1CCCSC1 KRQUFUKTQHISJB-YYADALCUSA-N 0.000 description 2
- FGRRPVNTIUYHOS-UHFFFAOYSA-N 3-iodoprop-2-ynyl n-cyclohexylcarbamate Chemical compound IC#CCOC(=O)NC1CCCCC1 FGRRPVNTIUYHOS-UHFFFAOYSA-N 0.000 description 2
- WNGHJMKXNAZRCS-UHFFFAOYSA-N 3-iodoprop-2-ynyl n-phenylcarbamate Chemical compound IC#CCOC(=O)NC1=CC=CC=C1 WNGHJMKXNAZRCS-UHFFFAOYSA-N 0.000 description 2
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical compound CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- CFKMVGJGLGKFKI-UHFFFAOYSA-N 4-chloro-m-cresol Chemical compound CC1=CC(O)=CC=C1Cl CFKMVGJGLGKFKI-UHFFFAOYSA-N 0.000 description 2
- BQMRHYBXRAYYQS-UHFFFAOYSA-N 4-dihydroxyphosphinothioyloxy-n,n-diethyl-6-methylpyrimidin-2-amine Chemical compound CCN(CC)C1=NC(C)=CC(OP(O)(O)=S)=N1 BQMRHYBXRAYYQS-UHFFFAOYSA-N 0.000 description 2
- NRTLIYOWLVMQBO-UHFFFAOYSA-N 5-chloro-1,3-dimethyl-N-(1,1,3-trimethyl-1,3-dihydro-2-benzofuran-4-yl)pyrazole-4-carboxamide Chemical compound C=12C(C)OC(C)(C)C2=CC=CC=1NC(=O)C=1C(C)=NN(C)C=1Cl NRTLIYOWLVMQBO-UHFFFAOYSA-N 0.000 description 2
- 239000005660 Abamectin Substances 0.000 description 2
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
- 239000005740 Boscalid Substances 0.000 description 2
- NYQDCVLCJXRDSK-UHFFFAOYSA-N Bromofos Chemical compound COP(=S)(OC)OC1=CC(Cl)=C(Br)C=C1Cl NYQDCVLCJXRDSK-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 2
- 239000005644 Dazomet Substances 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- YUBJPYNSGLJZPQ-UHFFFAOYSA-N Dithiopyr Chemical compound CSC(=O)C1=C(C(F)F)N=C(C(F)(F)F)C(C(=O)SC)=C1CC(C)C YUBJPYNSGLJZPQ-UHFFFAOYSA-N 0.000 description 2
- GUVLYNGULCJVDO-UHFFFAOYSA-N EPTC Chemical compound CCCN(CCC)C(=O)SCC GUVLYNGULCJVDO-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 239000005912 Lufenuron Substances 0.000 description 2
- 239000002169 Metam Substances 0.000 description 2
- LGDSHSYDSCRFAB-UHFFFAOYSA-N Methyl isothiocyanate Chemical compound CN=C=S LGDSHSYDSCRFAB-UHFFFAOYSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
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- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 description 1
- DQFPEYARZIQXRM-LTGZKZEYSA-N tralkoxydim Chemical compound C1C(=O)C(C(/CC)=N/OCC)=C(O)CC1C1=C(C)C=C(C)C=C1C DQFPEYARZIQXRM-LTGZKZEYSA-N 0.000 description 1
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- DBGVGMSCBYYSLD-UHFFFAOYSA-N tributylstannane Chemical compound CCCC[SnH](CCCC)CCCC DBGVGMSCBYYSLD-UHFFFAOYSA-N 0.000 description 1
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- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
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- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
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- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- WCJYTPVNMWIZCG-UHFFFAOYSA-N xylylcarb Chemical compound CNC(=O)OC1=CC=C(C)C(C)=C1 WCJYTPVNMWIZCG-UHFFFAOYSA-N 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical class [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- 229910000165 zinc phosphate Inorganic materials 0.000 description 1
- LPEBYPDZMWMCLZ-CVBJKYQLSA-L zinc;(z)-octadec-9-enoate Chemical class [Zn+2].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O LPEBYPDZMWMCLZ-CVBJKYQLSA-L 0.000 description 1
- IFNXAMCERSVZCV-UHFFFAOYSA-L zinc;2-ethylhexanoate Chemical class [Zn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O IFNXAMCERSVZCV-UHFFFAOYSA-L 0.000 description 1
- JDLYKQWJXAQNNS-UHFFFAOYSA-L zinc;dibenzoate Chemical class [Zn+2].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 JDLYKQWJXAQNNS-UHFFFAOYSA-L 0.000 description 1
- CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical class [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/08—Oxygen or sulfur directly attached to an aromatic ring system
-
- 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
- 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
- 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
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
-
- 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
- A01N55/08—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur containing boron
-
- 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
- A01N59/14—Boron; Compounds thereof
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
- B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
- B27K3/34—Organic impregnating agents
- B27K3/343—Heterocyclic compounds
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
- B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
- B27K3/34—Organic impregnating agents
- B27K3/38—Aromatic compounds
- B27K3/40—Aromatic compounds halogenated
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
- B27K2240/00—Purpose of the treatment
- B27K2240/20—Removing fungi, molds or insects
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- Pest Control & Pesticides (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Forests & Forestry (AREA)
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Claims (14)
1. Sammensætninger, der omfatter a) penflufen og dets salte eller syreadditionsforbindelser og b) mindst én forbindelse valgt fra gruppen bestående af o-phenylphenol og dens alkalimetal- og jordalkalimetalsalte, borforbindelser, forbindelser med formlen (II) ( (R1R2R3R4)N)nX (II) hvor R1 og R2 kan være ens eller forskellige og uafhængigt af hinanden står for Ci-C6-alkyl og R3 og R4 kan være ens eller forskellige og uafhængigt af hinanden er valgt fra gruppen bestående af C6-C22_alkyl, C6-C22-alkenyl, C6-C24-aryl, C5-C20-cycloalkyl, og grupper med formlen (IV) - [CH2CH2-0]z-CH2CH2-0H (IV) hvor z = 1, 2, 3, 4, 5, 6, 7, 8, 9 eller 10 og X betegner en anion, der bærer en ladning på n og n er et helt tal større end nul, isothiazolinoner, 3-iod-2-propynyl-N-butylcarbamat, 3-iod-2-propynyl-cycloalkylcarbamates, 3-iod-2-propynyl-arylcarbamater og forbindelser med formlen (III) (III) nvori
R5 betegner Cg-Cig-alkyl, Cg-Cig-alkenyl eller C5-C2o-cycloalkyl, og m og y kan være ens eller forskellige og repræsenterer et tal 1. 2, 3, 4, 5 eller 6, og deres syreadditionsforbindelser.
2. Sammensætning ifølge krav 1, kendetegnet ved, at borforbindelsen er valgt fra gruppen bestående af dinatriumtetraborat, decahydrat (borax), borsyre, borsyreestere, boroxid og dinatriumoctaborat, tetrahydrat.
3. Sammensætning ifølge mindst et af kravene 1 og 2, kendetegnet ved, at isothiazolinonen er valgt fra gruppen bestående af N-methylisothiazolin-3-on, 5-chlor-N- methylisothiazolin-3-on, 4,5-dichlor-N-octylisothiazolin-3-on, 5-chlor-N-octylisothiazolinon, N-octyl-isothiazolin-3-on, 4,5-trimethylen-isothiazolinon og 4,5-benzisothiazolinon.
4. Sammensætning ifølge mindst et af kravene 1 til 3, kendetegnet ved, at R3 og R4 i forbindelser med formlen (II) kan være identiske eller forskellige og uafhængigt af hinanden er valgt fra gruppen bestående af benzyl, -CH2CH2-O-CH2CH2-OH, -[CH2CH2-O] 2CH2CH2-OH, - [CH2CH2-O] 3-CH2CH2-OH, - [CH2CH2-O] 4-CH2CH2-OH, dichlorbenzyl, n-, isononyl, n-, isodecyl, n-, isododecyl, n-, isohexadecyl n-, isooctenyl, n-, isononenyl eller n-, isodecenyl og R1 og R2 betegner methyl.
5. Sammensætning ifølge mindst et af kravene 1 til 4, kendetegnet ved, at forbindelserne med formlen (III) er valgt fra gruppen bestående af N-(3-aminopropyl)-N-dodecyl-1,3-propandiamin, N-(3-aminopropyl)-N-decyl-1,3-propandiamin , N-(3-aminopropyl)-N-tetradecyl-1,3-propandiamin og deres syreadditionsforbindeIser.
6. Sammensætning ifølge mindst et af kravene 1 til 5, kendetegnet ved, at mindst 75 vægt-% - 85 vægt-% af penflufen og 15 vægt% - 25 vægt% af 3-iod-2-propynyl-N- butylcarbamat er til stede.
7. Sammensætning ifølge mindst et af kravene 1 til 6, kendetegnet ved, at mindst 50 vægt-% af penflufen og mindst 10 vægt-% af 4,5-dichlor-N-octylisothiazolin-3-on er til stede.
8. Sammensætninger ifølge et eller flere af kravene 1 til 7, kendetegnet ved, at de omfatter præparatet a) penflufen og dets salte eller syreadditionsforbindelser og b) mindst en forbindelse valgt fra gruppen bestående af o-phenylphenol og dens alkalimetal- og jordalkalimetalsalte natriumborat, borsyre, boroxid, benzalkoniumchlorid, didecyldimethylammoniumchlorid, didecylmethylpoly-(oxyethyl) ammoniumpropionat, didecyldimethylammoniumcarbonat, didecyldimethylammonium bicarbonat eller en blanding af didecyldimethylammoniumcarbonat og didecyldimethylammoniumbicarbonat 4,5-dichlor-N-octylisothiazolin-3-on, 3-iod-2-propynyl-N- butylcarbamat, N- (3-aminopropyl) -N-dodecyl-1,3-propandiamin.
9. Anvendelse af sammensætninger ifølge mindst et af kravene 1 til 8 til beskyttelse industrielle materialer mod angreb og/eller destruktion af mikroorganismer.
10. Anvendelse ifølge krav 9, kendetegnet ved, at det industrielle materiale er træ, et træprodukt eller en træplast komposit.
11. Anvendelse ifølge krav 10 til beskyttelse af træ, et træprodukt eller en træ-plast komposit mod træødelæggende Basidiomyceter, især Holobasidiomycetes.
12. Anvendelse ifølge krav 11 til beskyttelse af træ, et træprodukt eller en træ-plast komposit af træødelæggende Basidiomyceter, kendetegnet ved, at de træødelæggende Basidiomyceter er arter af slægterne Gloeophyllum, Coniophora, Coriolus, Stereum eller Poria.
13. Industrielle materialer, især træ, et produkttræ eller en træ-plast komposit, der omfatter a) penflufen og dets salte eller syreadditionsforbindelser og b) mindst én forbindelse valgt fra gruppen bestående af o-phenylphenol og dens alkalimetal- og jordalkalimetalsalte, borforbindelser, forbindelser med formlen (II) ( (R1R2R3R4)N)nX (II) hvor R1 og R2 kan være ens eller forskellige og uafhængigt af hinanden står for Ci-C6-alkyl og R3 og R4 kan være ens eller forskellige og uafhængigt af hinanden er valgt fra gruppen bestående af C6-C22-alkyl, C6-C22-alkenyl, C6-C24-aryl, C5-C2o-cycloalkyl, og grupper med (IV) med formlen - [CH2CH2-0] z-CH2CH2-OH (IV) hvor z = 1, 2, 3, 4, 5, 6, 7, 8, 9 eller 10 og X betegner en anion, der bærer en ladning på n og n er et helt tal større end nul, isothiazolinoner, 3-iod-2-propynyl-N-butylcarbamat, 3-iod-2- propynyl cycloalkylcarbamater, 3-iod-2-propynyl-arylcarbamat og forbindelser med formlen (III)
(III) hvori R5 betegner Cs-Cis-alkyl, Cs-Cis-alkenyl eller C5-C2o-cycloalkyl, og m og y kan være ens eller forskellige og repræsenterer et tal 1, 2, 3, 4, 5 eller 6, og deres syreadditionsforbindelser.
14. Proces til beskyttelse industrielle materialer mod angreb og/eller destruktion af mikroorganismer, kendetegnet ved, at mindst en sammensætning, der omfatter a) penflufen og dets salte eller syreadditionssalte af forbindelserne, og b) mindst én forbindelse valgt fra gruppen bestående af o-phenylphenol og dens alkalimetal- og jordalkalimetalsalte, borforbindelser, forbindelser med formlen (II) ( (R1R2R3R4)N)nX (II) hvor R1 og R2 kan være ens eller forskellige og uafhængigt af hinanden står for Ci-C6_alkyl og R3 og R4 kan være ens eller forskellige og uafhængigt af hinanden er valgt fra gruppen bestående af C6-C22-alkyl, C6-C22-alkenyl, C6-C24-aryl, C5-C20-cycloalkyl, og grupper med formlen (IV) - [CH2CH2-0] z-CH2CH2-OH (IV) hvor z = 1, 2, 3, 4, 5, 6, 7, 8, 9 eller 10 og X betegner en anion, der bærer en ladning på n og n er et helt tal større end nul, isothiazolinoner, 3-iod-2-propynyl-N-butylcarbamat, 3-iod-2- propynyl cycloalkylcarbamater, 3-iod-2-propynyl-arylcarbamat og forbindelser med formlen (III)
(III) hvori R5 betegner Cg-Cig-alkyl, C8-Ci8-alkenyl eller C5-C2o_cycloalkyl, og m og y kan være ens eller forskellige og repræsenterer et tal 1, 2, 3, 4, 5 eller 6, og deres syreadditionsforbindelser, lades virke på mikroorganismen eller dens levested.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10188713A EP2443928A1 (de) | 2010-10-25 | 2010-10-25 | Fungizide Penflufen Mischungen |
| EP10190017 | 2010-11-04 | ||
| PCT/EP2011/067165 WO2012055674A1 (de) | 2010-10-25 | 2011-09-30 | Fungizide penflufen mischungen |
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| DK2632267T3 true DK2632267T3 (da) | 2016-12-12 |
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| DK11764728.9T DK2632267T3 (da) | 2010-10-25 | 2011-09-30 | Svampedræbende penflufen-blandinger |
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| IT1403275B1 (it) | 2010-12-20 | 2013-10-17 | Isagro Ricerca Srl | Indanilanilidi ad elevata attività fungicida e loro composizioni fitosanitarie |
| ITMI20121045A1 (it) | 2012-06-15 | 2013-12-16 | Isagro Ricerca Srl | Composizioni sinergiche per la protezione di colture agrarie e relativo uso |
| US20160286805A1 (en) * | 2012-11-19 | 2016-10-06 | Arch Wood Protection, Inc. | Succinate dehydrogenase inhibitor containing compositions |
| US11039617B2 (en) | 2013-01-30 | 2021-06-22 | Agrofresh Inc. | Large scale methods of uniformly coating packaging surfaces with a volatile antimicrobial to preserve food freshness |
| US10070649B2 (en) | 2013-01-30 | 2018-09-11 | Agrofresh Inc. | Volatile applications against pathogens |
| CN103329905B (zh) * | 2013-07-24 | 2014-08-27 | 安徽省农业科学院植物保护与农产品质量安全研究所 | 一种含氟唑菌苯胺和井冈霉素的杀菌组合物 |
| CN105028459A (zh) * | 2015-07-14 | 2015-11-11 | 江西正邦生物化工有限责任公司 | 含有氟唑菌苯胺与噻虫嗪的种子处理可分散粒剂及其制备方法 |
| CN108207970A (zh) * | 2015-08-31 | 2018-06-29 | 陕西西大华特科技实业有限公司 | 一种含噻霉酮和吡噻菌胺的杀菌组合物、农药及其应用 |
| ES2783248T3 (es) * | 2015-09-02 | 2020-09-17 | Lanxess Deutschland Gmbh | Partículas de polímero que contienen penflufen |
| MX376636B (es) * | 2015-09-02 | 2025-03-07 | Lanxess Deutschland Gmbh | Mezclas biocidas |
| NZ745681A (en) | 2016-03-07 | 2022-05-27 | Agrofresh Inc | Synergistic methods of using benzoxaborole compounds and preservative gases as an antimicrobial for crops |
| EP3478070B1 (en) * | 2016-06-30 | 2020-04-22 | Dow Global Technologies LLC | Synergistic combination of 3-iodo-2-propynyl-butylcarbamate and diamine |
| MX2019007033A (es) | 2016-12-16 | 2019-12-19 | Koppers Performance Chemicals Inc | Preservante para madera y metodo para producirlo. |
| 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 |
| CN108908594B (zh) * | 2018-08-02 | 2020-09-08 | 安徽信达家居有限公司 | 一种延长防霉型竹材有效时间的处理方法 |
| RU2701941C1 (ru) * | 2018-11-26 | 2019-10-02 | Государственное бюджетное учреждение Республики Башкортостан "Научно-исследовательский технологический институт гербицидов и регуляторов роста растений с опытно-экспериментальным производством Академии наук Республики Башкортостан" | Фунгицидное средство |
| KR102176682B1 (ko) * | 2020-09-14 | 2020-11-09 | (주)서해씨엔씨 | 하이브리드 광촉매 살균제의 제조방법 및 그에 의해 제조된 하이브리드 광촉매 살균제 |
| DE102021003200A1 (de) * | 2021-06-22 | 2022-12-22 | Giesecke+Devrient Currency Technology Gmbh | Biozides Papier, biozides Wertdokument und Verfahren zu seiner Herstellung |
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| ATE357138T1 (de) * | 2001-11-21 | 2007-04-15 | Altachem Pharma Ltd | Antipathogenische zusammensetzung verwendbar in der konservierung von blut |
| DE10349501A1 (de) * | 2003-10-23 | 2005-05-25 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
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| DE102005025989A1 (de) * | 2005-06-07 | 2007-01-11 | Bayer Cropscience Ag | Carboxamide |
| DE102005043138A1 (de) * | 2005-09-10 | 2007-03-15 | Lanxess Deutschland Gmbh | Fungizide Mischungen für den Holzschutz |
| WO2007110173A2 (de) | 2006-03-24 | 2007-10-04 | Bayer Cropscience Ag | Fungizide wirkstoffkombinationen |
| GB0615213D0 (en) | 2006-07-31 | 2006-09-06 | Syngenta Participations Ag | Fungicidal compounds and compositions |
| EP2000030A1 (de) * | 2007-06-06 | 2008-12-10 | Bayer CropScience AG | Fungizide Wirkstoffkombinationen |
| JP4944844B2 (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 |
| RU2527024C2 (ru) | 2008-01-15 | 2014-08-27 | Байер Кропсайенс Аг | Пестицидная композиция, содержащая производное тетразолилоксима и активное фунгицидное или инсектицидное вещество (варианты) и способ борьбы с фитопатагенными грибами или вредоносными насекомыми |
| BRPI0907490A2 (pt) | 2008-02-05 | 2015-07-14 | Basf Se | Mistura, composição pesticida, método para controlar pragas e/ou melhorar a saúde das plantas, e para proteção de material de propagação de plantas, e, material de propagação de plantas |
| JP2011511032A (ja) | 2008-02-05 | 2011-04-07 | ビーエーエスエフ ソシエタス・ヨーロピア | 植物体健康組成物 |
| WO2011051243A1 (en) * | 2009-10-29 | 2011-05-05 | Bayer Cropscience Ag | Active compound combinations |
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