IL95305A - Agrochemical compositions - Google Patents

Agrochemical compositions

Info

Publication number: IL95305A
Authority: IL; Israel
Prior art keywords: methyl; methoxyacrylate; phenyl; yloxy; fungicidal
Prior art date: 1989-09-01

Application number

IL9530590A

Other languages

English (en)

Hebrew (he)

Other versions

IL95305A0 (en

Original Assignee

Ici Plc

Priority date (The priority date 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 date listed.)

1989-09-01

Filing date

1990-08-06

Publication date

1994-11-28

1989-09-01 Priority claimed from GB898919833A external-priority patent/GB8919833D0/en

1990-04-09 Priority claimed from GB909007995A external-priority patent/GB9007995D0/en

1990-08-06 Application filed by Ici Plc filed Critical Ici Plc

1991-06-30 Publication of IL95305A0 publication Critical patent/IL95305A0/xx

1994-11-28 Publication of IL95305A publication Critical patent/IL95305A/en

Links

239000000203 mixture Substances 0.000 title claims abstract description 60
239000003905 agrochemical Substances 0.000 title description 2
239000004480 active ingredient Substances 0.000 claims abstract description 47
230000000855 fungicidal effect Effects 0.000 claims abstract description 23
230000002363 herbicidal effect Effects 0.000 claims abstract description 23
230000001105 regulatory effect Effects 0.000 claims abstract description 20
230000008635 plant growth Effects 0.000 claims abstract description 19
235000007164 Oryza sativa Nutrition 0.000 claims abstract description 15
235000009566 rice Nutrition 0.000 claims abstract description 15
239000007787 solid Substances 0.000 claims abstract description 8
238000009835 boiling Methods 0.000 claims abstract description 5
230000005484 gravity Effects 0.000 claims abstract description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 54
239000008187 granular material Substances 0.000 claims description 37
-1 isopropyl ester Chemical class 0.000 claims description 25
241000209094 Oryza Species 0.000 claims description 19
239000004009 herbicide Substances 0.000 claims description 18
241000196324 Embryophyta Species 0.000 claims description 16
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 15
238000000034 method Methods 0.000 claims description 14
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 13
150000001875 compounds Chemical class 0.000 claims description 13
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 10
ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 claims description 6
201000010099 disease Diseases 0.000 claims description 6
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 6
239000000417 fungicide Substances 0.000 claims description 6
229940055577 oleyl alcohol Drugs 0.000 claims description 6
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 claims description 6
125000000217 alkyl group Chemical group 0.000 claims description 5
230000012010 growth Effects 0.000 claims description 5
WROZTZHKRRNHBS-UHFFFAOYSA-N phenyl propaneperoxoate Chemical compound CCC(=O)OOC1=CC=CC=C1 WROZTZHKRRNHBS-UHFFFAOYSA-N 0.000 claims description 5
JWUCHKBSVLQQCO-UHFFFAOYSA-N 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol Chemical compound C=1C=C(F)C=CC=1C(C=1C(=CC=CC=1)F)(O)CN1C=NC=N1 JWUCHKBSVLQQCO-UHFFFAOYSA-N 0.000 claims description 4
STMIIPIFODONDC-UHFFFAOYSA-N 2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(O)(CCCC)CN1C=NC=N1 STMIIPIFODONDC-UHFFFAOYSA-N 0.000 claims description 4
WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical compound C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 claims description 4
241001450781 Bipolaris oryzae Species 0.000 claims description 4
239000005787 Flutriafol Substances 0.000 claims description 4
125000005907 alkyl ester group Chemical group 0.000 claims description 4
230000001276 controlling effect Effects 0.000 claims description 4
YPHMISFOHDHNIV-FSZOTQKASA-N cycloheximide Chemical compound C1[C@@H](C)C[C@H](C)C(=O)[C@@H]1[C@H](O)CC1CC(=O)NC(=O)C1 YPHMISFOHDHNIV-FSZOTQKASA-N 0.000 claims description 4
MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 claims description 4
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 claims description 4
229920006395 saturated elastomer Polymers 0.000 claims description 4
UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 claims description 4
241001330975 Magnaporthe oryzae Species 0.000 claims description 3
239000003795 chemical substances by application Substances 0.000 claims description 3
235000014113 dietary fatty acids Nutrition 0.000 claims description 3
238000001125 extrusion Methods 0.000 claims description 3
239000000194 fatty acid Substances 0.000 claims description 3
229930195729 fatty acid Natural products 0.000 claims description 3
150000004665 fatty acids Chemical class 0.000 claims description 3
230000002538 fungal effect Effects 0.000 claims description 3
238000005470 impregnation Methods 0.000 claims description 3
238000004519 manufacturing process Methods 0.000 claims description 3
MZYYKQOKDIRBEP-NBVRZTHBSA-N methyl (e)-3-methoxy-2-[2-(3-pyrimidin-2-yloxyphenoxy)phenyl]prop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC=CC(OC=2N=CC=CN=2)=C1 MZYYKQOKDIRBEP-NBVRZTHBSA-N 0.000 claims description 3
YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical compound OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 claims description 3
URDNHJIVMYZFRT-KGLIPLIRSA-N (2r,3r)-1-(2,4-dichlorophenyl)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)pentan-3-ol Chemical compound C([C@H]([C@H](O)C(C)(C)C)N1N=CN=C1)C1=CC=C(Cl)C=C1Cl URDNHJIVMYZFRT-KGLIPLIRSA-N 0.000 claims description 2
CXNPLSGKWMLZPZ-GIFSMMMISA-N (2r,3r,6s)-3-[[(3s)-3-amino-5-[carbamimidoyl(methyl)amino]pentanoyl]amino]-6-(4-amino-2-oxopyrimidin-1-yl)-3,6-dihydro-2h-pyran-2-carboxylic acid Chemical compound O1[C@@H](C(O)=O)[C@H](NC(=O)C[C@@H](N)CCN(C)C(N)=N)C=C[C@H]1N1C(=O)N=C(N)C=C1 CXNPLSGKWMLZPZ-GIFSMMMISA-N 0.000 claims description 2
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 2
WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 claims description 2
PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 claims description 2
VGPIBGGRCVEHQZ-UHFFFAOYSA-N 1-(biphenyl-4-yloxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC(C=C1)=CC=C1C1=CC=CC=C1 VGPIBGGRCVEHQZ-UHFFFAOYSA-N 0.000 claims description 2
XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 claims description 2
LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 claims description 2
WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 claims description 2
PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 claims description 2
PDQRQJVPEFGVRK-UHFFFAOYSA-N 2,1,3-benzothiadiazole Chemical compound C1=CC=CC2=NSN=C21 PDQRQJVPEFGVRK-UHFFFAOYSA-N 0.000 claims description 2
UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 claims description 2
125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims description 2
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 2
UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 claims description 2
FFISWZPYNKWIRR-UHFFFAOYSA-N 5-oxidophenazin-5-ium Chemical compound C1=CC=C2[N+]([O-])=C(C=CC=C3)C3=NC2=C1 FFISWZPYNKWIRR-UHFFFAOYSA-N 0.000 claims description 2
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 2
239000005747 Chlorothalonil Substances 0.000 claims description 2
241001529717 Corticium <basidiomycota> Species 0.000 claims description 2
239000005757 Cyproconazole Substances 0.000 claims description 2
239000005760 Difenoconazole Substances 0.000 claims description 2
OQOULEWDDRNBSG-UHFFFAOYSA-N Fenapanil Chemical compound C=1C=CC=CC=1C(CCCC)(C#N)CN1C=CN=C1 OQOULEWDDRNBSG-UHFFFAOYSA-N 0.000 claims description 2
239000005786 Flutolanil Substances 0.000 claims description 2
ULCWZQJLFZEXCS-KGLIPLIRSA-N Furconazole-cis Chemical compound O1[C@@H](OCC(F)(F)F)CC[C@@]1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 ULCWZQJLFZEXCS-KGLIPLIRSA-N 0.000 claims description 2
241000223218 Fusarium Species 0.000 claims description 2
241000221778 Fusarium fujikuroi Species 0.000 claims description 2
239000005795 Imazalil Substances 0.000 claims description 2
239000005639 Lauric acid Substances 0.000 claims description 2
239000005802 Mancozeb Substances 0.000 claims description 2
239000005807 Metalaxyl Substances 0.000 claims description 2
239000005642 Oleic acid Substances 0.000 claims description 2
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 2
239000005813 Penconazole Substances 0.000 claims description 2
239000005814 Pencycuron Substances 0.000 claims description 2
PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims description 2
JPFWJDMDPLEUBD-UHFFFAOYSA-N Polyoxin D Natural products OC1C(O)C(C(NC(=O)C(C(O)C(O)COC(N)=O)N)C(O)=O)OC1N1C(=O)NC(=O)C(C(O)=O)=C1 JPFWJDMDPLEUBD-UHFFFAOYSA-N 0.000 claims description 2
239000005820 Prochloraz Substances 0.000 claims description 2
239000005822 Propiconazole Substances 0.000 claims description 2
241001558929 Sclerotium <basidiomycota> Species 0.000 claims description 2
229940100389 Sulfonylurea Drugs 0.000 claims description 2
239000005839 Tebuconazole Substances 0.000 claims description 2
239000005840 Tetraconazole Substances 0.000 claims description 2
239000005845 Tolclofos-methyl Substances 0.000 claims description 2
239000005846 Triadimenol Substances 0.000 claims description 2
JARYYMUOCXVXNK-UHFFFAOYSA-N Validamycin A Natural products OC1C(O)C(OC2C(C(O)C(O)C(CO)O2)O)C(CO)CC1NC1C=C(CO)C(O)C(O)C1O JARYYMUOCXVXNK-UHFFFAOYSA-N 0.000 claims description 2
241001272684 Xanthomonas campestris pv. oryzae Species 0.000 claims description 2
241000589652 Xanthomonas oryzae Species 0.000 claims description 2
238000005054 agglomeration Methods 0.000 claims description 2
230000002776 aggregation Effects 0.000 claims description 2
230000001580 bacterial effect Effects 0.000 claims description 2
RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 claims description 2
MITFXPHMIHQXPI-UHFFFAOYSA-N benzoxaprofen Natural products N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 claims description 2
CXNPLSGKWMLZPZ-UHFFFAOYSA-N blasticidin-S Natural products O1C(C(O)=O)C(NC(=O)CC(N)CCN(C)C(N)=N)C=CC1N1C(=O)N=C(N)C=C1 CXNPLSGKWMLZPZ-UHFFFAOYSA-N 0.000 claims description 2
150000001768 cations Chemical class 0.000 claims description 2
CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 claims description 2
239000011248 coating agent Substances 0.000 claims description 2
238000000576 coating method Methods 0.000 claims description 2
UWQMKVBQKFHLCE-UHFFFAOYSA-N diclomezine Chemical compound C1=C(Cl)C(C)=C(Cl)C=C1C1=NNC(=O)C=C1 UWQMKVBQKFHLCE-UHFFFAOYSA-N 0.000 claims description 2
BQYJATMQXGBDHF-UHFFFAOYSA-N difenoconazole Chemical compound O1C(C)COC1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-UHFFFAOYSA-N 0.000 claims description 2
FBOUIAKEJMZPQG-BLXFFLACSA-N diniconazole-M Chemical compound C1=NC=NN1/C([C@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1Cl FBOUIAKEJMZPQG-BLXFFLACSA-N 0.000 claims description 2
AWZOLILCOUMRDG-UHFFFAOYSA-N edifenphos Chemical compound C=1C=CC=CC=1SP(=O)(OCC)SC1=CC=CC=C1 AWZOLILCOUMRDG-UHFFFAOYSA-N 0.000 claims description 2
229960002125 enilconazole Drugs 0.000 claims description 2
DWRKFAJEBUWTQM-UHFFFAOYSA-N etaconazole Chemical compound O1C(CC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 DWRKFAJEBUWTQM-UHFFFAOYSA-N 0.000 claims description 2
PTCGDEVVHUXTMP-UHFFFAOYSA-N flutolanil Chemical compound CC(C)OC1=CC=CC(NC(=O)C=2C(=CC=CC=2)C(F)(F)F)=C1 PTCGDEVVHUXTMP-UHFFFAOYSA-N 0.000 claims description 2
208000010801 foot rot Diseases 0.000 claims description 2
229910052736 halogen Inorganic materials 0.000 claims description 2
239000005556 hormone Substances 0.000 claims description 2
229940088597 hormone Drugs 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
KGVPNLBXJKTABS-UHFFFAOYSA-N hymexazol Chemical compound CC1=CC(O)=NO1 KGVPNLBXJKTABS-UHFFFAOYSA-N 0.000 claims description 2
FCOAHACKGGIURQ-UHFFFAOYSA-N iprobenfos Chemical compound CC(C)OP(=O)(OC(C)C)SCC1=CC=CC=C1 FCOAHACKGGIURQ-UHFFFAOYSA-N 0.000 claims description 2
WPOOICLZIIBUBM-UHFFFAOYSA-H iron;iron(3+);methyl-dioxido-oxo-$l^{5}-arsane Chemical compound [Fe].[Fe+3].[Fe+3].C[As]([O-])([O-])=O.C[As]([O-])([O-])=O.C[As]([O-])([O-])=O WPOOICLZIIBUBM-UHFFFAOYSA-H 0.000 claims description 2
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
UFHLMYOGRXOCSL-UHFFFAOYSA-N isoprothiolane Chemical compound CC(C)OC(=O)C(C(=O)OC(C)C)=C1SCCS1 UFHLMYOGRXOCSL-UHFFFAOYSA-N 0.000 claims description 2
PVTHJAPFENJVNC-MHRBZPPQSA-N kasugamycin Chemical compound N[C@H]1C[C@H](NC(=N)C(O)=O)[C@@H](C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H]1O PVTHJAPFENJVNC-MHRBZPPQSA-N 0.000 claims description 2
BCTQJXQXJVLSIG-UHFFFAOYSA-N mepronil Chemical compound CC(C)OC1=CC=CC(NC(=O)C=2C(=CC=CC=2)C)=C1 BCTQJXQXJVLSIG-UHFFFAOYSA-N 0.000 claims description 2
MARSFTCPBDWHCQ-SDNWHVSQSA-N methyl (e)-2-[2-[6-(2,6-difluorophenoxy)pyrimidin-4-yl]oxyphenyl]-3-methoxyprop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2F)F)=NC=N1 MARSFTCPBDWHCQ-SDNWHVSQSA-N 0.000 claims description 2
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 description 2
BLCKKNLGFULNRC-UHFFFAOYSA-L n,n-dimethylcarbamodithioate;nickel(2+) Chemical compound [Ni+2].CN(C)C([S-])=S.CN(C)C([S-])=S BLCKKNLGFULNRC-UHFFFAOYSA-L 0.000 claims description 2
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 2
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 2
OGYFATSSENRIKG-UHFFFAOYSA-N pencycuron Chemical compound C1=CC(Cl)=CC=C1CN(C(=O)NC=1C=CC=CC=1)C1CCCC1 OGYFATSSENRIKG-UHFFFAOYSA-N 0.000 claims description 2
JPFWJDMDPLEUBD-ITJAGOAWSA-N polyoxorim Polymers O[C@@H]1[C@H](O)[C@@H]([C@H](NC(=O)[C@H]([C@H](O)[C@@H](O)COC(N)=O)N)C(O)=O)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 JPFWJDMDPLEUBD-ITJAGOAWSA-N 0.000 claims description 2
WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 claims description 2
TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 claims description 2
STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 claims description 2
XRJLAOUDSILTFT-UHFFFAOYSA-N pyroquilon Chemical compound O=C1CCC2=CC=CC3=C2N1CC3 XRJLAOUDSILTFT-UHFFFAOYSA-N 0.000 claims description 2
229960005322 streptomycin Drugs 0.000 claims description 2
125000000547 substituted alkyl group Chemical group 0.000 claims description 2
125000003107 substituted aryl group Chemical group 0.000 claims description 2
ROZUQUDEWZIBHV-UHFFFAOYSA-N tecloftalam Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(=O)NC1=CC=CC(Cl)=C1Cl ROZUQUDEWZIBHV-UHFFFAOYSA-N 0.000 claims description 2
239000004308 thiabendazole Substances 0.000 claims description 2
235000010296 thiabendazole Nutrition 0.000 claims description 2
WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 claims description 2
229960004546 thiabendazole Drugs 0.000 claims description 2
OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 claims description 2
BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 claims description 2
DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 claims description 2
229940087291 tridecyl alcohol Drugs 0.000 claims description 2
JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 claims description 2
241000813090 Rhizoctonia solani Species 0.000 claims 2
125000005843 halogen group Chemical group 0.000 claims 2
125000006282 2-chlorobenzyl group Chemical group [H]C1=C([H])C(Cl)=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
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QIHOFSAVNYTADJ-LFIBNONCSA-N methyl (e)-2-[2-(3,5-dimethylbenzoyl)pyrrol-1-yl]-3-methoxyprop-2-enoate Chemical compound CO\C=C(/C(=O)OC)N1C=CC=C1C(=O)C1=CC(C)=CC(C)=C1 QIHOFSAVNYTADJ-LFIBNONCSA-N 0.000 description 1
VEJCBCPEURAYAS-JUEGYJDASA-N methyl (e)-3-methoxy-2-[2-(2-phenylethenyl)phenyl]prop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1C=CC1=CC=CC=C1 VEJCBCPEURAYAS-JUEGYJDASA-N 0.000 description 1
KSEAXFAHWCZDJZ-RVDMUPIBSA-N methyl (e)-3-methoxy-2-[2-[3-(1,1,2,2-tetrafluoroethoxy)phenoxy]phenyl]prop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC=CC(OC(F)(F)C(F)F)=C1 KSEAXFAHWCZDJZ-RVDMUPIBSA-N 0.000 description 1
BKLNXWIVUBHFKG-FOWTUZBSSA-N methyl (e)-3-methoxy-2-[2-[6-(6-methylpyridin-2-yl)oxypyrimidin-4-yl]oxyphenyl]prop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2N=C(C)C=CC=2)=NC=N1 BKLNXWIVUBHFKG-FOWTUZBSSA-N 0.000 description 1
238000003801 milling Methods 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
DUWWHGPELOTTOE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(OC)=C(NC(=O)CC(C)=O)C=C1Cl DUWWHGPELOTTOE-UHFFFAOYSA-N 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
229910017604 nitric acid Inorganic materials 0.000 description 1
ZWLPBLYKEWSWPD-UHFFFAOYSA-N o-toluic acid Chemical compound CC1=CC=CC=C1C(O)=O ZWLPBLYKEWSWPD-UHFFFAOYSA-N 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
230000002688 persistence Effects 0.000 description 1
229920001983 poloxamer Polymers 0.000 description 1
239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
239000004540 pour-on Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
238000009666 routine test Methods 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
238000007873 sieving Methods 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
235000017550 sodium carbonate Nutrition 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
239000011973 solid acid Substances 0.000 description 1
241000894007 species Species 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000005720 sucrose Substances 0.000 description 1
235000000346 sugar Nutrition 0.000 description 1
150000008163 sugars Chemical class 0.000 description 1
239000001117 sulphuric acid Chemical class 0.000 description 1
235000011149 sulphuric acid Nutrition 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000008399 tap water Substances 0.000 description 1
235000020679 tap water Nutrition 0.000 description 1
QERYCTSHXKAMIS-UHFFFAOYSA-M thiophene-2-carboxylate Chemical compound [O-]C(=O)C1=CC=CS1 QERYCTSHXKAMIS-UHFFFAOYSA-M 0.000 description 1
150000003626 triacylglycerols Chemical class 0.000 description 1
229960002415 trichloroethylene Drugs 0.000 description 1
239000000341 volatile oil Substances 0.000 description 1
239000003232 water-soluble binding agent Substances 0.000 description 1
229920003169 water-soluble polymer Polymers 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/12—Powders or granules
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/12—Powders or granules
- A01N25/14—Powders or granules wettable

Landscapes

Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Toxicology (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Agronomy & Crop Science (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Investigating Or Analyzing Materials By The Use Of Ultrasonic Waves (AREA)

IL9530590A 1989-09-01 1990-08-06 Agrochemical compositions IL95305A (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB898919833A GB8919833D0 (en)	1989-09-01	1989-09-01	Agrochemical composition
GB909007995A GB9007995D0 (en)	1990-04-09	1990-04-09	Fungicidal and plant growth regulating compositions

Publications (2)

Publication Number	Publication Date
IL95305A0 IL95305A0 (en)	1991-06-30
IL95305A true IL95305A (en)	1994-11-28

Family

ID=26295851

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL9530590A IL95305A (en)	1989-09-01	1990-08-06	Agrochemical compositions

Country Status (16)

Country	Link
US (1)	US5466693A (de)
EP (1)	EP0415569B1 (de)
JP (1)	JP2880778B2 (de)
KR (1)	KR0157416B1 (de)
CN (1)	CN1044070C (de)
AT (1)	ATE167778T1 (de)
AU (1)	AU642151B2 (de)
CA (1)	CA2023547A1 (de)
DE (1)	DE69032449T2 (de)
ES (1)	ES2117626T3 (de)
GB (1)	GB9016783D0 (de)
HU (1)	HUT57536A (de)
IL (1)	IL95305A (de)
MY (1)	MY106843A (de)
PH (1)	PH31202A (de)
PT (1)	PT95163A (de)

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JP3350863B2 (ja) *	1991-04-26	2002-11-25	ダウ・ケミカル日本株式会社	水田除草用粒剤組成物
GB9202378D0 (en) *	1992-02-05	1992-03-18	Sandoz Ltd	Inventions relating to fungicidal compositions
GB9210830D0 (en) *	1992-05-21	1992-07-08	Ici Plc	Fungicidial composition
EP0581095A2 (de) *	1992-07-24	1994-02-02	BASF Aktiengesellschaft	Substituierte Acrylsäureester und diese enthaltende Pflanzenschutzmittel
JPH06336402A (ja) *	1993-05-26	1994-12-06	Nippon Nohyaku Co Ltd	稲紋枯病防除組成物
US5580544A (en) *	1995-03-29	1996-12-03	Uniroyal Chemical Company, Inc.	Paste formulation useful for seed treatment and foliar treatment of plants
US5833733A (en) *	1995-05-12	1998-11-10	Nihon Bayer Agrochem K.K.	Agrochemical formulations for water surface application
JP3772994B2 (ja) *	1995-06-22	2006-05-10	バイエルクロップサイエンス株式会社	水田用農薬粒剤
US5830827A (en) *	1995-09-21	1998-11-03	Ishihara Sangyo Kaisha, Ltd.	Granular herbicidal composition comprising flazasulfuron and a sulfosuccinate or benzoate stabilizer
US5706292A (en) *	1996-04-25	1998-01-06	Micron Technology, Inc.	Layout for a semiconductor memory device having redundant elements
DE69821940T2 (de)	1997-06-30	2005-03-17	Monsanto Technology Llc	Landwirtschaftlich aktive inhaltsstoffe enthaltende mikropartikel
WO2000015637A1 (en) *	1998-09-16	2000-03-23	Dow Agrosciences Llc	2-methoxyimino -2-(pyridinyloxymethyl) phenyl acetamides with 5 membered heterocyclic rings on the pyridine ring as fungicides
WO2000015616A1 (en)	1998-09-16	2000-03-23	Dow Agrosciences Llc	2-methoxyimino-2-(pyridinyloxymethyl)phenyl acetamides with (derivatised) hydroxyalkyl derivatives on the pyridine ring
US6369083B1 (en)	1998-09-16	2002-04-09	Dow Agrosciences Llc	2-methoxyimino-2 (pyrinyloxymethyl) phenyl acetamides with polyether derivatives on the pyridine ring
WO2001035738A2 (en)	1999-11-18	2001-05-25	Basf Corporation	Non-aqueous concentrated spreading oil composition
CA2393377A1 (en)	1999-12-15	2001-06-21	Neil Vincent Kirby	Compounds having fungicidal activity and processes to produce and use same
CN100455567C (zh) *	2005-04-07	2009-01-28	曾小华	用作渔药的二硫代氨基甲酸铁族金属盐
KR100700504B1 (ko) *	2005-05-17	2007-03-28	한국화학연구원	알킬 지방산 에스터를 함유하는 식물병 방제용 조성물
WO2007031133A1 (en) *	2005-07-14	2007-03-22	Bayer Healthcare Ag	Pharmaceutical composition
ZA200802442B (en)	2005-09-01	2010-02-24	Du Pont	Liquid sulfonylurea herbicide formulations
KR100769363B1 (ko) *	2006-04-12	2007-10-31	대한민국	파라콰트계 저항성 망초류 방제용 스클레로티엄 델피니비더블유씨04-107 균주 및 이를 이용하여 제조되는 균사체현탁액
US20080004189A1 (en) *	2006-06-29	2008-01-03	Weatherford/Lamb, Inc.	Effervescent biocide compositions for oilfield applications
PT2046123E (pt) *	2006-07-24	2014-11-18	Syngenta Participations Ag	Grânulos de libertação controlada
WO2008041118A2 (en)	2006-10-04	2008-04-10	Pfizer Products Inc.	Pyrido[4,3-d]pyrimidin-4(3h)-one derivatives as calcium receptor antagonists
US9992999B2 (en) *	2008-04-01	2018-06-12	Sepro Corporation	Solid aquatic herbicide formulations
AU2009263037B2 (en) *	2008-06-26	2011-10-06	Amgen Inc.	Alkynyl alcohols as kinase inhibitors
EP2723175B1 (de) *	2011-06-22	2017-05-17	Dow AgroSciences LLC	Herbizide granulate mit integriertem adjuvans
CN102657198B (zh) *	2012-05-08	2014-03-19	陕西上格之路生物科学有限公司	一种含苯肽胺酸的杀菌增产组合物
CN103120172A (zh) *	2013-02-04	2013-05-29	广东中迅农科股份有限公司	一种用于防除水稻田杂草的漂浮颗粒剂
CN114081032B (zh) *	2015-03-03	2025-03-28	阿尔萨达新西兰有限公司	用于改善发芽和开花的组合物
CN107568257B (zh) *	2017-08-18	2020-06-26	广东省农业科学院农业生物基因研究中心	一种提高水稻种子结实率的配方及其制备方法和应用

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1990
- 1990-07-31 GB GB909016783A patent/GB9016783D0/en active Pending
- 1990-08-01 ES ES90308478T patent/ES2117626T3/es not_active Expired - Lifetime
- 1990-08-01 DE DE69032449T patent/DE69032449T2/de not_active Expired - Fee Related
- 1990-08-01 EP EP90308478A patent/EP0415569B1/de not_active Expired - Lifetime
- 1990-08-01 AT AT90308478T patent/ATE167778T1/de not_active IP Right Cessation
- 1990-08-06 AU AU60220/90A patent/AU642151B2/en not_active Ceased
- 1990-08-06 IL IL9530590A patent/IL95305A/en not_active IP Right Cessation
- 1990-08-10 HU HU904960A patent/HUT57536A/hu unknown
- 1990-08-13 PH PH41016A patent/PH31202A/en unknown
- 1990-08-17 CA CA002023547A patent/CA2023547A1/en not_active Abandoned
- 1990-08-30 MY MYPI90001496A patent/MY106843A/en unknown
- 1990-08-31 PT PT95163A patent/PT95163A/pt not_active Application Discontinuation
- 1990-08-31 JP JP2228511A patent/JP2880778B2/ja not_active Expired - Lifetime
- 1990-09-01 KR KR1019900013799A patent/KR0157416B1/ko not_active Expired - Fee Related
- 1990-09-01 CN CN90107234A patent/CN1044070C/zh not_active Expired - Fee Related
1993
- 1993-09-23 US US08/125,702 patent/US5466693A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
PT95163A (pt)	1991-05-22
AU642151B2 (en)	1993-10-14
MY106843A (en)	1995-08-30
CN1049771A (zh)	1991-03-13
KR910005755A (ko)	1991-04-27
ES2117626T3 (es)	1998-08-16
EP0415569A3 (en)	1992-10-28
DE69032449D1 (de)	1998-08-06
ATE167778T1 (de)	1998-07-15
JP2880778B2 (ja)	1999-04-12
EP0415569B1 (de)	1998-07-01
AU6022090A (en)	1991-03-07
CA2023547A1 (en)	1991-03-02
HU904960D0 (en)	1991-01-28
PH31202A (en)	1998-05-05
GB9016783D0 (en)	1990-09-12
CN1044070C (zh)	1999-07-14
IL95305A0 (en)	1991-06-30
US5466693A (en)	1995-11-14
HUT57536A (en)	1991-12-30
DE69032449T2 (de)	1999-01-07
KR0157416B1 (ko)	1998-10-15
JPH03193705A (ja)	1991-08-23
EP0415569A2 (de)	1991-03-06

Legal Events

Date	Code	Title	Description
1997-06-10	RH	Patent void

Publication	Publication Date	Title
US5466693A (en)	1995-11-14	Granular fungicidal composition for application to an aquatic environment
RU2083107C1 (ru)	1997-07-10	Гербицидное синергитическое средство, способ поражения нежелательных растений
US5236887A (en)	1993-08-17	Herbicidal heterocyclic sulfonylurea compositions safened by herbicidal acids such as 2,4-d below a ph of 5
CN104387157A (zh)	2015-03-04	颗粒控释农用化学品组合物及其制备方法
CN105072901A (zh)	2015-11-18	除草组合物及其使用方法
JP2913214B2 (ja)	1999-06-28	植物の生長を調節するための相乗作用組成物
JPH07506589A (ja)	1995-07-20	殺菌剤組成物
CN1126448C (zh)	2003-11-05	作为吡氟禾草灵辅剂和活化剂的肌氨酸盐
JP2002363004A (ja)	2002-12-18	徐放性農薬粒剤およびその施用方法
JPH03148201A (ja)	1991-06-25	水田施用殺虫剤組成物、その製造法及び稲害虫の防除方法
JPH0768087B2 (ja)	1995-07-26	除草剤組成物
WO2022264064A1 (en)	2022-12-22	Novaluron water dispersible solid composition
JPH10330202A (ja)	1998-12-15	水性懸濁状除草剤組成物及び雑草防除方法
KR0168491B1 (ko)	1999-01-15	수면 살포용 살충제 조성물
JPH0232004A (ja)	1990-02-01	除草組成物
WO2025173008A1 (en)	2025-08-21	Solid formulation
JP5019570B2 (ja)	2012-09-05	芝病害防除組成物
JPH09124403A (ja)	1997-05-13	水面施用農薬液状製剤組成物及びその使用方法
JP2008056602A (ja)	2008-03-13	芝病害防除組成物
EP2178368A2 (de)	2010-04-28	Verfahren zur bekämpfung von pollenkäfern
JP2008127288A (ja)	2008-06-05	水稲直播栽培の除草方法
JPH05112412A (ja)	1993-05-07	農園芸用殺菌剤
WO1998036642A1 (en)	1998-08-27	Herbicide compositions
JPH0232005A (ja)	1990-02-01	除草剤組成物
JPS6379804A (ja)	1988-04-09	水田用除草剤組成物