JP2009504585A5 - - Google Patents
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- Publication number
- JP2009504585A5 JP2009504585A5 JP2008525453A JP2008525453A JP2009504585A5 JP 2009504585 A5 JP2009504585 A5 JP 2009504585A5 JP 2008525453 A JP2008525453 A JP 2008525453A JP 2008525453 A JP2008525453 A JP 2008525453A JP 2009504585 A5 JP2009504585 A5 JP 2009504585A5
- Authority
- JP
- Japan
- Prior art keywords
- salt
- phosphorous acid
- copper
- zinc
- titanium dioxide
- 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.)
- Pending
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- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical class C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims 95
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims 48
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical class [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 claims 39
- 239000000203 mixture Substances 0.000 claims 38
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims 34
- 239000010949 copper Substances 0.000 claims 30
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims 26
- DCYOBGZUOMKFPA-UHFFFAOYSA-N iron(2+);iron(3+);octadecacyanide Chemical compound [Fe+2].[Fe+2].[Fe+2].[Fe+3].[Fe+3].[Fe+3].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] DCYOBGZUOMKFPA-UHFFFAOYSA-N 0.000 claims 24
- 229960003351 prussian blue Drugs 0.000 claims 24
- 239000013225 prussian blue Substances 0.000 claims 24
- 239000004408 titanium dioxide Substances 0.000 claims 24
- 150000003751 zinc Chemical class 0.000 claims 22
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 claims 20
- 229960001138 acetylsalicylic acid Drugs 0.000 claims 20
- -1 alkali metal salt Chemical class 0.000 claims 17
- 239000011787 zinc oxide Substances 0.000 claims 17
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims 13
- 229960004889 salicylic acid Drugs 0.000 claims 13
- 159000000007 calcium salts Chemical class 0.000 claims 12
- 150000001875 compounds Chemical class 0.000 claims 11
- 150000003839 salts Chemical class 0.000 claims 11
- 230000002195 synergetic effect Effects 0.000 claims 9
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical group [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 claims 8
- 230000000855 fungicidal effect Effects 0.000 claims 7
- 238000000034 method Methods 0.000 claims 6
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims 6
- 235000012239 silicon dioxide Nutrition 0.000 claims 6
- 241000233866 Fungi Species 0.000 claims 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 4
- 239000011701 zinc Substances 0.000 claims 4
- 229910052725 zinc Inorganic materials 0.000 claims 4
- PLXMOAALOJOTIY-FPTXNFDTSA-N Aesculin Natural products OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@H](O)[C@H]1Oc2cc3C=CC(=O)Oc3cc2O PLXMOAALOJOTIY-FPTXNFDTSA-N 0.000 claims 3
- WNBCMONIPIJTSB-BGNCJLHMSA-N Cichoriin Natural products O([C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1)c1c(O)cc2c(OC(=O)C=C2)c1 WNBCMONIPIJTSB-BGNCJLHMSA-N 0.000 claims 3
- 241000196324 Embryophyta Species 0.000 claims 3
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims 3
- 229910052783 alkali metal Inorganic materials 0.000 claims 3
- XHCADAYNFIFUHF-TVKJYDDYSA-N esculin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC(C(=C1)O)=CC2=C1OC(=O)C=C2 XHCADAYNFIFUHF-TVKJYDDYSA-N 0.000 claims 3
- 229940093496 esculin Drugs 0.000 claims 3
- AWRMZKLXZLNBBK-UHFFFAOYSA-N esculin Natural products OC1OC(COc2cc3C=CC(=O)Oc3cc2O)C(O)C(O)C1O AWRMZKLXZLNBBK-UHFFFAOYSA-N 0.000 claims 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 3
- 229910052748 manganese Inorganic materials 0.000 claims 3
- 239000011572 manganese Substances 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims 3
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 claims 3
- 244000000003 plant pathogen Species 0.000 claims 3
- PCCSBWNGDMYFCW-UHFFFAOYSA-N 5-methyl-5-(4-phenoxyphenyl)-3-(phenylamino)-1,3-oxazolidine-2,4-dione Chemical compound O=C1C(C)(C=2C=CC(OC=3C=CC=CC=3)=CC=2)OC(=O)N1NC1=CC=CC=C1 PCCSBWNGDMYFCW-UHFFFAOYSA-N 0.000 claims 2
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 claims 2
- 239000005750 Copper hydroxide Substances 0.000 claims 2
- 239000005752 Copper oxychloride Substances 0.000 claims 2
- WAEMQWOKJMHJLA-UHFFFAOYSA-N Manganese(2+) Chemical class [Mn+2] WAEMQWOKJMHJLA-UHFFFAOYSA-N 0.000 claims 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 2
- 229910052782 aluminium Inorganic materials 0.000 claims 2
- 150000003863 ammonium salts Chemical class 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical compound [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 claims 2
- 229910052802 copper Inorganic materials 0.000 claims 2
- 229910001956 copper hydroxide Inorganic materials 0.000 claims 2
- HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 claims 2
- 229910052742 iron Inorganic materials 0.000 claims 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 2
- ZQEIXNIJLIKNTD-GFCCVEGCSA-N metalaxyl-M Chemical compound COCC(=O)N([C@H](C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-GFCCVEGCSA-N 0.000 claims 2
- 229910052759 nickel Inorganic materials 0.000 claims 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims 2
- 230000003287 optical effect Effects 0.000 claims 2
- HZRSNVGNWUDEFX-UHFFFAOYSA-N pyraclostrobin Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 HZRSNVGNWUDEFX-UHFFFAOYSA-N 0.000 claims 2
- 239000000377 silicon dioxide Substances 0.000 claims 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 claims 2
- ONDPHDOFVYQSGI-UHFFFAOYSA-N zinc nitrate Chemical compound [Zn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ONDPHDOFVYQSGI-UHFFFAOYSA-N 0.000 claims 2
- XERJKGMBORTKEO-VZUCSPMQSA-N (1e)-2-(ethylcarbamoylamino)-n-methoxy-2-oxoethanimidoyl cyanide Chemical compound CCNC(=O)NC(=O)C(\C#N)=N\OC XERJKGMBORTKEO-VZUCSPMQSA-N 0.000 claims 1
- OQEBBZSWEGYTPG-GSVOUGTGSA-N (3r)-3-aminobutanoic acid Chemical compound C[C@@H](N)CC(O)=O OQEBBZSWEGYTPG-GSVOUGTGSA-N 0.000 claims 1
- QNBTYORWCCMPQP-JXAWBTAJSA-N (Z)-dimethomorph Chemical compound C1=C(OC)C(OC)=CC=C1C(\C=1C=CC(Cl)=CC=1)=C/C(=O)N1CCOCC1 QNBTYORWCCMPQP-JXAWBTAJSA-N 0.000 claims 1
- KMHSUNDEGHRBNV-UHFFFAOYSA-N 2,4-dichloropyrimidine-5-carbonitrile Chemical compound ClC1=NC=C(C#N)C(Cl)=N1 KMHSUNDEGHRBNV-UHFFFAOYSA-N 0.000 claims 1
- YFFGVSAXBMXABA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-4-(trifluoromethyl)benzoic acid Chemical compound C1=C(OC)C(OC)=CC=C1C1=CC(C(F)(F)F)=CC=C1C(O)=O YFFGVSAXBMXABA-UHFFFAOYSA-N 0.000 claims 1
- KWLVWJPJKJMCSH-UHFFFAOYSA-N 2-(4-chlorophenyl)-N-{2-[3-methoxy-4-(prop-2-yn-1-yloxy)phenyl]ethyl}-2-(prop-2-yn-1-yloxy)acetamide Chemical compound C1=C(OCC#C)C(OC)=CC(CCNC(=O)C(OCC#C)C=2C=CC(Cl)=CC=2)=C1 KWLVWJPJKJMCSH-UHFFFAOYSA-N 0.000 claims 1
- FYRZOZGETUESPQ-UHFFFAOYSA-N 2-chloro-n-(2,6-dimethylphenyl)-n-(5-oxooxolan-3-yl)acetamide Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)C1CC(=O)OC1 FYRZOZGETUESPQ-UHFFFAOYSA-N 0.000 claims 1
- 125000003762 3,4-dimethoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 claims 1
- SOUGWDPPRBKJEX-UHFFFAOYSA-N 3,5-dichloro-N-(1-chloro-3-methyl-2-oxopentan-3-yl)-4-methylbenzamide Chemical compound ClCC(=O)C(C)(CC)NC(=O)C1=CC(Cl)=C(C)C(Cl)=C1 SOUGWDPPRBKJEX-UHFFFAOYSA-N 0.000 claims 1
- KGTYUUJBKGRXBP-UHFFFAOYSA-N 3-(1-chloro-3-methyl-2-oxopentan-3-yl)-4-methylbenzamide Chemical compound ClCC(C(C)(CC)C1=C(C=CC(=C1)C(=O)N)C)=O KGTYUUJBKGRXBP-UHFFFAOYSA-N 0.000 claims 1
- MPTYXKQJSCYQPW-UHFFFAOYSA-N 3-(dimethylamino)hexyl carbamate Chemical compound CCCC(N(C)C)CCOC(N)=O MPTYXKQJSCYQPW-UHFFFAOYSA-N 0.000 claims 1
- OQEBBZSWEGYTPG-UHFFFAOYSA-N 3-Aminobutanoic acid Natural products CC(N)CC(O)=O OQEBBZSWEGYTPG-UHFFFAOYSA-N 0.000 claims 1
- QDUDFMMPZWYGFP-UHFFFAOYSA-N 3-anilino-5-methyl-2-methylsulfanyl-5-phenylimidazolidin-4-one Chemical compound CSC1NC(C)(C=2C=CC=CC=2)C(=O)N1NC1=CC=CC=C1 QDUDFMMPZWYGFP-UHFFFAOYSA-N 0.000 claims 1
- PXHWLMUSVTVOMH-UHFFFAOYSA-N 4-chloro-2-cyano-N,N-bis(methylamino)-5-(4-methylphenyl)imidazole-1-sulfonamide Chemical compound C(#N)C=1N(C(=C(N=1)Cl)C1=CC=C(C=C1)C)S(N(NC)NC)(=O)=O PXHWLMUSVTVOMH-UHFFFAOYSA-N 0.000 claims 1
- CJIJXIFQYOPWTF-UHFFFAOYSA-N 7-hydroxycoumarin Natural products O1C(=O)C=CC2=CC(O)=CC=C21 CJIJXIFQYOPWTF-UHFFFAOYSA-N 0.000 claims 1
- 239000005964 Acibenzolar-S-methyl Substances 0.000 claims 1
- 239000005730 Azoxystrobin Substances 0.000 claims 1
- 239000005734 Benalaxyl Substances 0.000 claims 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 claims 1
- 239000005739 Bordeaux mixture Substances 0.000 claims 1
- QQMFZDGGOOVCBD-UHFFFAOYSA-N CC[S+]1N=C(C(Cl)(Cl)Cl)N=C1OC1=NC(C(Cl)(Cl)Cl)=N[S+]1CC Chemical compound CC[S+]1N=C(C(Cl)(Cl)Cl)N=C1OC1=NC(C(Cl)(Cl)Cl)=N[S+]1CC QQMFZDGGOOVCBD-UHFFFAOYSA-N 0.000 claims 1
- 239000005747 Chlorothalonil Substances 0.000 claims 1
- VMQMZMRVKUZKQL-UHFFFAOYSA-N Cu+ Chemical class [Cu+] VMQMZMRVKUZKQL-UHFFFAOYSA-N 0.000 claims 1
- 241000219104 Cucurbitaceae Species 0.000 claims 1
- 239000005761 Dimethomorph Substances 0.000 claims 1
- 108010016626 Dipeptides Proteins 0.000 claims 1
- 239000005769 Etridiazole Substances 0.000 claims 1
- 239000005772 Famoxadone Substances 0.000 claims 1
- 239000005780 Fluazinam Substances 0.000 claims 1
- 239000005789 Folpet Substances 0.000 claims 1
- 239000005802 Mancozeb Substances 0.000 claims 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims 1
- 239000005807 Metalaxyl Substances 0.000 claims 1
- 239000005808 Metalaxyl-M Substances 0.000 claims 1
- NQRFDNJEBWAUBL-UHFFFAOYSA-N N-[cyano(2-thienyl)methyl]-4-ethyl-2-(ethylamino)-1,3-thiazole-5-carboxamide Chemical compound S1C(NCC)=NC(CC)=C1C(=O)NC(C#N)C1=CC=CS1 NQRFDNJEBWAUBL-UHFFFAOYSA-N 0.000 claims 1
- 244000061176 Nicotiana tabacum Species 0.000 claims 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 claims 1
- 240000007594 Oryza sativa Species 0.000 claims 1
- 235000007164 Oryza sativa Nutrition 0.000 claims 1
- 239000005869 Pyraclostrobin Substances 0.000 claims 1
- 235000021536 Sugar beet Nutrition 0.000 claims 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims 1
- 241000219094 Vitaceae Species 0.000 claims 1
- 239000005863 Zoxamide Substances 0.000 claims 1
- MCMNRKCIXSYSNV-UHFFFAOYSA-N ZrO2 Inorganic materials O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims 1
- UELITFHSCLAHKR-UHFFFAOYSA-N acibenzolar-S-methyl Chemical group CSC(=O)C1=CC=CC2=C1SN=N2 UELITFHSCLAHKR-UHFFFAOYSA-N 0.000 claims 1
- QNHQEUFMIKRNTB-UHFFFAOYSA-N aesculetin Natural products C1CC(=O)OC2=C1C=C(O)C(O)=C2 QNHQEUFMIKRNTB-UHFFFAOYSA-N 0.000 claims 1
- GUAFOGOEJLSQBT-UHFFFAOYSA-N aesculetin dimethyl ether Natural products C1=CC(=O)OC2=C1C=C(OC)C(OC)=C2 GUAFOGOEJLSQBT-UHFFFAOYSA-N 0.000 claims 1
- 239000003242 anti bacterial agent Substances 0.000 claims 1
- 230000000843 anti-fungal effect Effects 0.000 claims 1
- 229940088710 antibiotic agent Drugs 0.000 claims 1
- WFDXOXNFNRHQEC-GHRIWEEISA-N azoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C#N)=NC=N1 WFDXOXNFNRHQEC-GHRIWEEISA-N 0.000 claims 1
- CJPQIRJHIZUAQP-MRXNPFEDSA-N benalaxyl-M Chemical compound CC=1C=CC=C(C)C=1N([C@H](C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-MRXNPFEDSA-N 0.000 claims 1
- SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 claims 1
- 235000013339 cereals Nutrition 0.000 claims 1
- 235000019804 chlorophyll Nutrition 0.000 claims 1
- 229930002875 chlorophyll Natural products 0.000 claims 1
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 claims 1
- 235000019805 chlorophyllin Nutrition 0.000 claims 1
- 229940099898 chlorophyllin Drugs 0.000 claims 1
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 claims 1
- 239000012141 concentrate Substances 0.000 claims 1
- 229910000365 copper sulfate Inorganic materials 0.000 claims 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 claims 1
- CMDYHTIDHSNRGW-UHFFFAOYSA-L copper;2-acetyloxybenzoate Chemical compound [Cu+2].CC(=O)OC1=CC=CC=C1C([O-])=O.CC(=O)OC1=CC=CC=C1C([O-])=O CMDYHTIDHSNRGW-UHFFFAOYSA-L 0.000 claims 1
- 239000013078 crystal Substances 0.000 claims 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 claims 1
- 239000000975 dye Substances 0.000 claims 1
- 235000013399 edible fruits Nutrition 0.000 claims 1
- 239000000839 emulsion Substances 0.000 claims 1
- ILEDWLMCKZNDJK-UHFFFAOYSA-N esculetin Chemical compound C1=CC(=O)OC2=C1C=C(O)C(O)=C2 ILEDWLMCKZNDJK-UHFFFAOYSA-N 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- AWYFNIZYMPNGAI-UHFFFAOYSA-L ethylenebis(dithiocarbamate) Chemical compound [S-]C(=S)NCCNC([S-])=S AWYFNIZYMPNGAI-UHFFFAOYSA-L 0.000 claims 1
- KQTVWCSONPJJPE-UHFFFAOYSA-N etridiazole Chemical compound CCOC1=NC(C(Cl)(Cl)Cl)=NS1 KQTVWCSONPJJPE-UHFFFAOYSA-N 0.000 claims 1
- 239000003337 fertilizer Substances 0.000 claims 1
- UZCGKGPEKUCDTF-UHFFFAOYSA-N fluazinam Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=NC=C(C(F)(F)F)C=C1Cl UZCGKGPEKUCDTF-UHFFFAOYSA-N 0.000 claims 1
- 239000000417 fungicide Substances 0.000 claims 1
- 239000008187 granular material Substances 0.000 claims 1
- 235000021021 grapes Nutrition 0.000 claims 1
- 239000004009 herbicide Substances 0.000 claims 1
- 239000004615 ingredient Substances 0.000 claims 1
- 239000002917 insecticide Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 claims 1
- CJPQIRJHIZUAQP-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(phenylacetyl)alaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-UHFFFAOYSA-N 0.000 claims 1
- 239000004530 micro-emulsion Substances 0.000 claims 1
- 239000002105 nanoparticle Substances 0.000 claims 1
- YQYKFSVTESXLFN-UHFFFAOYSA-N o-methyl 1,2,3-benzothiadiazole-7-carbothioate Chemical compound COC(=S)C1=CC=CC2=C1SN=N2 YQYKFSVTESXLFN-UHFFFAOYSA-N 0.000 claims 1
- UWVQIROCRJWDKL-UHFFFAOYSA-N oxadixyl Chemical compound CC=1C=CC=C(C)C=1N(C(=O)COC)N1CCOC1=O UWVQIROCRJWDKL-UHFFFAOYSA-N 0.000 claims 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 claims 1
- 239000002245 particle Substances 0.000 claims 1
- NUNQWODPVJYIDK-UHFFFAOYSA-N phenyl 3-methoxyprop-2-enoate Chemical compound COC=CC(=O)OC1=CC=CC=C1 NUNQWODPVJYIDK-UHFFFAOYSA-N 0.000 claims 1
- 230000001699 photocatalysis Effects 0.000 claims 1
- 239000000049 pigment Substances 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 230000001376 precipitating effect Effects 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- 235000009566 rice Nutrition 0.000 claims 1
- 239000002689 soil Substances 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 238000007614 solvation Methods 0.000 claims 1
- 238000009331 sowing Methods 0.000 claims 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical class C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 claims 1
- 239000000725 suspension Substances 0.000 claims 1
- 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 claims 1
- ORHBXUUXSCNDEV-UHFFFAOYSA-N umbelliferone Chemical compound C1=CC(=O)OC2=CC(O)=CC=C21 ORHBXUUXSCNDEV-UHFFFAOYSA-N 0.000 claims 1
- HFTAFOQKODTIJY-UHFFFAOYSA-N umbelliferone Natural products Cc1cc2C=CC(=O)Oc2cc1OCC=CC(C)(C)O HFTAFOQKODTIJY-UHFFFAOYSA-N 0.000 claims 1
- 235000013311 vegetables Nutrition 0.000 claims 1
- 239000004563 wettable powder Substances 0.000 claims 1
- 239000011592 zinc chloride Substances 0.000 claims 1
- 235000005074 zinc chloride Nutrition 0.000 claims 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 claims 1
- 229910000368 zinc sulfate Inorganic materials 0.000 claims 1
- 229960001763 zinc sulfate Drugs 0.000 claims 1
Applications Claiming Priority (2)
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|---|---|---|---|
| IT001558A ITMI20051558A1 (it) | 2005-08-09 | 2005-08-09 | Miscele e-o composizioni sinergiche cin elevata attivita'fungicida |
| PCT/EP2006/007784 WO2007017220A2 (en) | 2005-08-09 | 2006-08-04 | Synergistic mixtures and/or compositions with a high fungicidal activity |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009504585A JP2009504585A (ja) | 2009-02-05 |
| JP2009504585A5 true JP2009504585A5 (https=) | 2009-09-17 |
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| EP (1) | EP1912506A2 (https=) |
| JP (1) | JP2009504585A (https=) |
| CN (1) | CN101291585A (https=) |
| BR (1) | BRPI0614339A2 (https=) |
| IT (1) | ITMI20051558A1 (https=) |
| WO (1) | WO2007017220A2 (https=) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5101836B2 (ja) * | 2006-05-10 | 2012-12-19 | 幸一 島田 | 農薬、抗糸状菌薬剤、及び作物の栽培方法 |
| US20100291229A1 (en) * | 2009-05-12 | 2010-11-18 | Sipcam Argo Usa, Inc. | Fungicidal compositions and methods of enhancing plants such as turfgrass |
| ES2930370T3 (es) | 2009-10-08 | 2022-12-09 | Delos Living Llc | Sistema de iluminación LED |
| CN101755765B (zh) * | 2009-11-10 | 2013-02-27 | 深圳诺普信农化股份有限公司 | 含有活化酯的杀菌组合物 |
| EP2680698B1 (en) * | 2011-03-03 | 2015-01-28 | DSM IP Assets B.V. | New antifungal compositions |
| MX388775B (es) | 2011-05-04 | 2025-03-20 | Stewart Benson Averett | Composiciones fotocatalíticas de dióxido de titanio y sus usos. |
| JP5938253B2 (ja) * | 2012-03-30 | 2016-06-22 | 大日精化工業株式会社 | 紺青組成物 |
| CN102669131A (zh) * | 2012-05-24 | 2012-09-19 | 利民化工股份有限公司 | 一种嘧菌酯与灭菌丹复配的悬浮剂及其制备方法 |
| US9451770B2 (en) * | 2012-06-08 | 2016-09-27 | Charles Despres | Method of activating immune response in plants |
| ES2781873T3 (es) | 2012-08-28 | 2020-09-08 | Delos Living Llc | Sistemas y métodos para mejorar el bienestar asociado con ambientes habitables |
| US9474282B2 (en) | 2013-12-13 | 2016-10-25 | Tony John Hall | Acid-solubilized copper-ammonium complexes and copper-zinc-ammonium complexes, compositions, preparations, methods, and uses |
| CA2940766A1 (en) | 2014-02-28 | 2015-09-03 | Delos Living Llc | Systems, methods and articles for enhancing wellness associated with habitable environments |
| WO2015185994A1 (en) * | 2014-06-03 | 2015-12-10 | Myco Sciences Limited | Anti-microbial compositions, preparations, methods, and uses |
| EP3160233A4 (en) | 2014-06-23 | 2018-03-07 | Well Shield LLC | Reduction of infections in healthcare settings using photocatalytic compositions |
| EP3245631A4 (en) | 2015-01-13 | 2018-06-27 | Delos Living, LLC | Systems, methods and articles for monitoring and enhancing human wellness |
| KR102669720B1 (ko) | 2015-06-08 | 2024-05-27 | 브이엠 애그리테크 리미티드 | 항미생물 및 농화학 조성물 |
| WO2018039433A1 (en) | 2016-08-24 | 2018-03-01 | Delos Living Llc | Systems, methods and articles for enhancing wellness associated with habitable environments |
| WO2019046580A1 (en) | 2017-08-30 | 2019-03-07 | Delos Living Llc | SYSTEMS, METHODS AND ARTICLES FOR EVALUATING AND / OR IMPROVING HEALTH AND WELL-BEING |
| WO2019077460A1 (en) * | 2017-10-17 | 2019-04-25 | Upl Ltd | NEW AGROCHEMICAL COMBINATIONS |
| US11649977B2 (en) | 2018-09-14 | 2023-05-16 | Delos Living Llc | Systems and methods for air remediation |
| US11844163B2 (en) | 2019-02-26 | 2023-12-12 | Delos Living Llc | Method and apparatus for lighting in an office environment |
| US11898898B2 (en) | 2019-03-25 | 2024-02-13 | Delos Living Llc | Systems and methods for acoustic monitoring |
| CN110026238A (zh) * | 2019-05-24 | 2019-07-19 | 中国石油大学(华东) | 一种纳米棒状光催化材料及制备方法 |
| CN112056319B (zh) * | 2020-09-09 | 2021-09-24 | 中农立华生物科技股份有限公司 | 一种苯噻菌胺与亚磷酸盐的复配杀菌剂及其应用 |
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| TR19072A (tr) * | 1973-11-26 | 1978-05-01 | Pepro | Fosforlu tuerevler ihtiva eden fungisid terkipler |
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| CY1247A (en) | 1979-08-16 | 1984-08-31 | Sandoz Ltd | N-acylamino-2-oxo-3-oxazolidine derivatives and their use as fungicides |
| JPS6052146B2 (ja) | 1979-12-25 | 1985-11-18 | 石原産業株式会社 | Ｎ−ピリジルアニリン系化合物、それらの製造方法及びそれらを含有する有害生物防除剤 |
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| EP0230209A3 (de) * | 1985-12-16 | 1987-08-12 | Ciba-Geigy Ag | Mikrobizide |
| DE3788100T2 (de) * | 1986-08-26 | 1994-04-21 | Nippon Kayaku Kk | Verfahren zum Adsorbieren und Zersetzen von Ethylen und/oder anderen, in der Luft oder anderen geruchserzeugenden Quellen vorliegenden Geruchsubstanzen. |
| US4917820A (en) * | 1986-08-26 | 1990-04-17 | Nippon Kayaku Kabushiki Kaisha | Ethylene removal agent, postharvest preservation agent and deodorant |
| EP0313512B1 (de) | 1987-08-21 | 1992-11-25 | Ciba-Geigy Ag | Benzothiadiazole und ihre Verwendung in Verfahren und Mitteln gegen Pflanzenkrankheiten |
| IL91418A (en) | 1988-09-01 | 1997-11-20 | Rhone Poulenc Agrochimie | (hetero) cyclic amide derivatives, process for their preparation and fungicidal compositions containing them |
| GB8903019D0 (en) | 1989-02-10 | 1989-03-30 | Ici Plc | Fungicides |
| CN1052023A (zh) * | 1990-06-16 | 1991-06-12 | 王代春 | 植物用腐霉丹高效杀菌营养剂 |
| DE4026966A1 (de) | 1990-08-25 | 1992-02-27 | Bayer Ag | Substituierte valinamid-derivate |
| US5185242A (en) | 1991-06-24 | 1993-02-09 | Becton Dickinson And Company | Method for lysing mycobacteria using achromopeptidase |
| FR2706456B1 (fr) | 1993-06-18 | 1996-06-28 | Rhone Poulenc Agrochimie | Dérivés optiquement actifs de 2-imidazoline-5-ones et 2-imidazoline-5-thiones fongicides. |
| FR2701259B1 (fr) | 1993-02-08 | 1995-03-24 | Rhone Poulenc Agrochimie | Procédé pour la préparation de dérivés phénylbenzamides fongicides agricoles. |
| US5846554A (en) * | 1993-11-15 | 1998-12-08 | Zeneca Limited | Microcapsules containing suspensions of biologically active compounds and ultraviolet protectant |
| DE4423613A1 (de) | 1994-07-06 | 1996-01-11 | Basf Ag | 2-[1',2',4'-Triazol-3'yloxymethylen]-anilide, Verfahren zu ihrer Herstellung und ihre Verwendung |
| US5723491A (en) | 1994-07-11 | 1998-03-03 | Novartis Corporation | Fungicidal composition and method of controlling fungus infestation |
| PL182711B1 (pl) | 1994-08-03 | 2002-02-28 | Ihara Chemical Industry Coltd | Nowe pochodne amidów aminokwasów oraz fungicydy dla rolnictwa lub ogrodnictwa |
| DE69513657T2 (de) | 1994-09-08 | 2000-04-06 | Ishihara Sangyo Kaisha Ltd. | Verfahren zur Herstellung von 1-substituierten 2-Cyanoimidazolen |
| US5599804A (en) * | 1995-04-03 | 1997-02-04 | Rhone-Poulenc, Inc. | Fungicidal compositions for the enhancement of turf quality |
| AU721611B2 (en) | 1995-07-12 | 2000-07-13 | Gowan Comercio Internacional E Servicos, Limitada | Method for controlling phytopathogenic fungi |
| CN1225972C (zh) | 1996-12-19 | 2005-11-09 | 伊萨格罗股份公司 | 基于(n－苯乙酰基－n－2,6－二甲苯基)氨基丙酸甲酯的杀真菌组合物 |
| WO2002060248A2 (en) * | 2001-01-29 | 2002-08-08 | Agricare Ltd. | Methods and compositions for controlling plant pathogen |
| ITMI20022516A1 (it) * | 2002-11-27 | 2004-05-28 | Isagro Spa | Composizioni fungicide. |
-
2005
- 2005-08-09 IT IT001558A patent/ITMI20051558A1/it unknown
-
2006
- 2006-08-04 BR BRPI0614339-3A patent/BRPI0614339A2/pt not_active IP Right Cessation
- 2006-08-04 WO PCT/EP2006/007784 patent/WO2007017220A2/en not_active Ceased
- 2006-08-04 CN CNA2006800354902A patent/CN101291585A/zh active Pending
- 2006-08-04 US US11/989,994 patent/US20100197495A1/en not_active Abandoned
- 2006-08-04 JP JP2008525453A patent/JP2009504585A/ja active Pending
- 2006-08-04 EP EP06762997A patent/EP1912506A2/en not_active Withdrawn
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