JP5363328B2 - 除草組成物 - Google Patents
除草組成物 Download PDFInfo
- Publication number
- JP5363328B2 JP5363328B2 JP2009533734A JP2009533734A JP5363328B2 JP 5363328 B2 JP5363328 B2 JP 5363328B2 JP 2009533734 A JP2009533734 A JP 2009533734A JP 2009533734 A JP2009533734 A JP 2009533734A JP 5363328 B2 JP5363328 B2 JP 5363328B2
- Authority
- JP
- Japan
- Prior art keywords
- composition
- composition according
- solvent
- alcohol
- adjuvant
- 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.)
- Active
Links
- 239000000203 mixture Substances 0.000 title claims description 96
- 230000002363 herbicidal effect Effects 0.000 title claims description 10
- 239000002671 adjuvant Substances 0.000 claims description 38
- -1 Alkyl sulfate salt Chemical class 0.000 claims description 31
- 239000005597 Pinoxaden Substances 0.000 claims description 26
- MGOHCFMYLBAPRN-UHFFFAOYSA-N pinoxaden Chemical compound CCC1=CC(C)=CC(CC)=C1C(C1=O)=C(OC(=O)C(C)(C)C)N2N1CCOCC2 MGOHCFMYLBAPRN-UHFFFAOYSA-N 0.000 claims description 26
- 239000002904 solvent Substances 0.000 claims description 17
- 239000004009 herbicide Substances 0.000 claims description 16
- 239000000126 substance Substances 0.000 claims description 14
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 claims description 12
- 239000003995 emulsifying agent Substances 0.000 claims description 12
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims description 10
- GTVWRXDRKAHEAD-UHFFFAOYSA-N Tris(2-ethylhexyl) phosphate Chemical compound CCCCC(CC)COP(=O)(OCC(CC)CCCC)OCC(CC)CCCC GTVWRXDRKAHEAD-UHFFFAOYSA-N 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 9
- 150000002148 esters Chemical class 0.000 claims description 9
- 239000001089 [(2R)-oxolan-2-yl]methanol Substances 0.000 claims description 8
- 239000000839 emulsion Substances 0.000 claims description 8
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 claims description 6
- 239000005529 Florasulam Substances 0.000 claims description 6
- QZXATCCPQKOEIH-UHFFFAOYSA-N Florasulam Chemical compound N=1N2C(OC)=NC=C(F)C2=NC=1S(=O)(=O)NC1=C(F)C=CC=C1F QZXATCCPQKOEIH-UHFFFAOYSA-N 0.000 claims description 6
- SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 claims description 6
- KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 claims description 6
- 239000012141 concentrate Substances 0.000 claims description 6
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 claims description 6
- 150000003839 salts Chemical group 0.000 claims description 6
- 239000002202 Polyethylene glycol Substances 0.000 claims description 5
- 150000001298 alcohols Chemical class 0.000 claims description 5
- 230000015556 catabolic process Effects 0.000 claims description 5
- 235000013339 cereals Nutrition 0.000 claims description 5
- 238000006731 degradation reaction Methods 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 229920001223 polyethylene glycol Polymers 0.000 claims description 5
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 4
- 239000003924 oil dispersant Substances 0.000 claims description 4
- 239000000600 sorbitol Substances 0.000 claims description 4
- 238000003860 storage Methods 0.000 claims description 4
- 239000004548 suspo-emulsion Substances 0.000 claims description 4
- LPEKGGXMPWTOCB-UHFFFAOYSA-N 8beta-(2,3-epoxy-2-methylbutyryloxy)-14-acetoxytithifolin Natural products COC(=O)C(C)O LPEKGGXMPWTOCB-UHFFFAOYSA-N 0.000 claims description 3
- 239000005498 Clodinafop Substances 0.000 claims description 3
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 3
- 239000005507 Diflufenican Substances 0.000 claims description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 3
- 239000005558 Fluroxypyr Substances 0.000 claims description 3
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 claims description 3
- 150000001412 amines Chemical group 0.000 claims description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 3
- ZYTLPUIDJRKAAM-UHFFFAOYSA-N benzyl 2-hydroxypropanoate Chemical compound CC(O)C(=O)OCC1=CC=CC=C1 ZYTLPUIDJRKAAM-UHFFFAOYSA-N 0.000 claims description 3
- 235000019445 benzyl alcohol Nutrition 0.000 claims description 3
- 229960002903 benzyl benzoate Drugs 0.000 claims description 3
- YUIKUTLBPMDDNQ-MRVPVSSYSA-N clodinafop Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=NC=C(Cl)C=C1F YUIKUTLBPMDDNQ-MRVPVSSYSA-N 0.000 claims description 3
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 claims description 3
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 3
- WYEHFWKAOXOVJD-UHFFFAOYSA-N diflufenican Chemical compound FC1=CC(F)=CC=C1NC(=O)C1=CC=CN=C1OC1=CC=CC(C(F)(F)F)=C1 WYEHFWKAOXOVJD-UHFFFAOYSA-N 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
- MEFQWPUMEMWTJP-UHFFFAOYSA-N fluroxypyr Chemical compound NC1=C(Cl)C(F)=NC(OCC(O)=O)=C1Cl MEFQWPUMEMWTJP-UHFFFAOYSA-N 0.000 claims description 3
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims description 3
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 claims description 3
- 239000000344 soap Substances 0.000 claims description 3
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 claims description 3
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 claims description 3
- MZHCENGPTKEIGP-RXMQYKEDSA-N (R)-dichlorprop Chemical compound OC(=O)[C@@H](C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-RXMQYKEDSA-N 0.000 claims description 2
- RBSXHDIPCIWOMG-UHFFFAOYSA-N 1-(4,6-dimethoxypyrimidin-2-yl)-3-(2-ethylsulfonylimidazo[1,2-a]pyridin-3-yl)sulfonylurea Chemical compound CCS(=O)(=O)C=1N=C2C=CC=CN2C=1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 RBSXHDIPCIWOMG-UHFFFAOYSA-N 0.000 claims description 2
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 claims description 2
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 claims description 2
- MZHCENGPTKEIGP-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-UHFFFAOYSA-N 0.000 claims description 2
- WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 claims description 2
- MAYMYMXYWIVVOK-UHFFFAOYSA-N 2-[(4,6-dimethoxypyrimidin-2-yl)carbamoylsulfamoyl]-4-(methanesulfonamidomethyl)benzoic acid Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(CNS(C)(=O)=O)C=2)C(O)=O)=N1 MAYMYMXYWIVVOK-UHFFFAOYSA-N 0.000 claims description 2
- UWHURBUBIHUHSU-UHFFFAOYSA-N 2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 UWHURBUBIHUHSU-UHFFFAOYSA-N 0.000 claims description 2
- LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 claims description 2
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 claims description 2
- 239000003666 Amidosulfuron Substances 0.000 claims description 2
- CTTHWASMBLQOFR-UHFFFAOYSA-N Amidosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)N(C)S(C)(=O)=O)=N1 CTTHWASMBLQOFR-UHFFFAOYSA-N 0.000 claims description 2
- 239000005711 Benzoic acid Substances 0.000 claims description 2
- 239000005489 Bromoxynil Substances 0.000 claims description 2
- MRABAEUHTLLEML-UHFFFAOYSA-N Butyl lactate Chemical compound CCCCOC(=O)C(C)O MRABAEUHTLLEML-UHFFFAOYSA-N 0.000 claims description 2
- 239000005496 Chlorsulfuron Substances 0.000 claims description 2
- 239000005500 Clopyralid Substances 0.000 claims description 2
- 239000005505 Dichlorprop-P Substances 0.000 claims description 2
- RXCPQSJAVKGONC-UHFFFAOYSA-N Flumetsulam Chemical compound N1=C2N=C(C)C=CN2N=C1S(=O)(=O)NC1=C(F)C=CC=C1F RXCPQSJAVKGONC-UHFFFAOYSA-N 0.000 claims description 2
- QBEXFUOWUYCXNI-UHFFFAOYSA-N Ioxynil octanoate Chemical compound CCCCCCCC(=O)OC1=C(I)C=C(C#N)C=C1I QBEXFUOWUYCXNI-UHFFFAOYSA-N 0.000 claims description 2
- 239000005574 MCPA Substances 0.000 claims description 2
- 239000005575 MCPB Substances 0.000 claims description 2
- 101150039283 MCPB gene Proteins 0.000 claims description 2
- 239000005577 Mesosulfuron Substances 0.000 claims description 2
- 239000005591 Pendimethalin Substances 0.000 claims description 2
- 239000005603 Prosulfocarb Substances 0.000 claims description 2
- 239000005604 Prosulfuron Substances 0.000 claims description 2
- LTUNNEGNEKBSEH-UHFFFAOYSA-N Prosulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)CCC(F)(F)F)=N1 LTUNNEGNEKBSEH-UHFFFAOYSA-N 0.000 claims description 2
- 229940100389 Sulfonylurea Drugs 0.000 claims description 2
- 239000005619 Sulfosulfuron Substances 0.000 claims description 2
- GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 claims description 2
- 239000005624 Tralkoxydim Substances 0.000 claims description 2
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 claims description 2
- 239000005629 Tritosulfuron Substances 0.000 claims description 2
- 125000004104 aryloxy group Chemical group 0.000 claims description 2
- 235000010233 benzoic acid Nutrition 0.000 claims description 2
- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 claims description 2
- VJYIFXVZLXQVHO-UHFFFAOYSA-N chlorsulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)Cl)=N1 VJYIFXVZLXQVHO-UHFFFAOYSA-N 0.000 claims description 2
- HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 claims description 2
- OILAIQUEIWYQPH-UHFFFAOYSA-N cyclohexane-1,2-dione Chemical compound O=C1CCCCC1=O OILAIQUEIWYQPH-UHFFFAOYSA-N 0.000 claims description 2
- OPGCOAPTHCZZIW-UHFFFAOYSA-N diethyl 1-(2,4-dichlorophenyl)-5-methyl-4h-pyrazole-3,5-dicarboxylate Chemical group CCOC(=O)C1(C)CC(C(=O)OCC)=NN1C1=CC=C(Cl)C=C1Cl OPGCOAPTHCZZIW-UHFFFAOYSA-N 0.000 claims description 2
- COYBRKAVBMYYSF-UHFFFAOYSA-N heptan-2-yl [(5-chloroquinolin-8-yl)oxy]acetate Chemical group C1=CN=C2C(OCC(=O)OC(C)CCCCC)=CC=C(Cl)C2=C1 COYBRKAVBMYYSF-UHFFFAOYSA-N 0.000 claims description 2
- 230000002401 inhibitory effect Effects 0.000 claims description 2
- NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 claims description 2
- MWKVXOJATACCCH-UHFFFAOYSA-N isoxadifen-ethyl Chemical group C1C(C(=O)OCC)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 MWKVXOJATACCCH-UHFFFAOYSA-N 0.000 claims description 2
- LZGUHMNOBNWABZ-UHFFFAOYSA-N n-nitro-n-phenylnitramide Chemical compound [O-][N+](=O)N([N+]([O-])=O)C1=CC=CC=C1 LZGUHMNOBNWABZ-UHFFFAOYSA-N 0.000 claims description 2
- 150000002825 nitriles Chemical class 0.000 claims description 2
- 229940049964 oleate Drugs 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
- CHIFOSRWCNZCFN-UHFFFAOYSA-N pendimethalin Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 claims description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical compound OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 claims description 2
- 230000008635 plant growth Effects 0.000 claims description 2
- NQLVQOSNDJXLKG-UHFFFAOYSA-N prosulfocarb Chemical compound CCCN(CCC)C(=O)SCC1=CC=CC=C1 NQLVQOSNDJXLKG-UHFFFAOYSA-N 0.000 claims description 2
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 claims description 2
- KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 claims description 2
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 claims description 2
- LOQQVLXUKHKNIA-UHFFFAOYSA-N thifensulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C2=C(SC=C2)C(O)=O)=N1 LOQQVLXUKHKNIA-UHFFFAOYSA-N 0.000 claims description 2
- 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 claims description 2
- YWBFPKPWMSWWEA-UHFFFAOYSA-O triazolopyrimidine Chemical compound BrC1=CC=CC(C=2N=C3N=CN[N+]3=C(NCC=3C=CN=CC=3)C=2)=C1 YWBFPKPWMSWWEA-UHFFFAOYSA-O 0.000 claims description 2
- 229940087291 tridecyl alcohol Drugs 0.000 claims description 2
- 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 claims description 2
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 claims description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 229920001400 block copolymer Polymers 0.000 claims 2
- 239000001191 butyl (2R)-2-hydroxypropanoate Substances 0.000 claims 2
- IEORSVTYLWZQJQ-UHFFFAOYSA-N 2-(2-nonylphenoxy)ethanol Chemical compound CCCCCCCCCC1=CC=CC=C1OCCO IEORSVTYLWZQJQ-UHFFFAOYSA-N 0.000 claims 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 claims 1
- 239000005625 Tri-allate Substances 0.000 claims 1
- MWBPRDONLNQCFV-UHFFFAOYSA-N Tri-allate Chemical compound CC(C)N(C(C)C)C(=O)SCC(Cl)=C(Cl)Cl MWBPRDONLNQCFV-UHFFFAOYSA-N 0.000 claims 1
- 239000005626 Tribenuron Substances 0.000 claims 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 claims 1
- 229940043264 dodecyl sulfate Drugs 0.000 claims 1
- DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 claims 1
- 229940100242 glycol stearate Drugs 0.000 claims 1
- 229940057867 methyl lactate Drugs 0.000 claims 1
- 229920000847 nonoxynol Polymers 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 1
- BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 description 13
- 229910019142 PO4 Inorganic materials 0.000 description 12
- 239000003921 oil Substances 0.000 description 12
- 235000019198 oils Nutrition 0.000 description 12
- 235000021317 phosphate Nutrition 0.000 description 12
- 238000002156 mixing Methods 0.000 description 11
- 238000009472 formulation Methods 0.000 description 10
- 239000010452 phosphate Substances 0.000 description 10
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 241000196324 Embryophyta Species 0.000 description 8
- 238000010348 incorporation Methods 0.000 description 8
- 239000007921 spray Substances 0.000 description 8
- 240000008042 Zea mays Species 0.000 description 6
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 6
- 125000001931 aliphatic group Chemical group 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 235000019484 Rapeseed oil Nutrition 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 238000011161 development Methods 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 238000010353 genetic engineering Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- 239000005562 Glyphosate Substances 0.000 description 3
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 3
- 238000009395 breeding Methods 0.000 description 3
- 230000001488 breeding effect Effects 0.000 description 3
- 235000005822 corn Nutrition 0.000 description 3
- 244000038559 crop plants Species 0.000 description 3
- 230000002708 enhancing effect Effects 0.000 description 3
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 3
- 229940097068 glyphosate Drugs 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 235000009973 maize Nutrition 0.000 description 3
- 239000011159 matrix material Substances 0.000 description 3
- 150000004702 methyl esters Chemical class 0.000 description 3
- 239000003094 microcapsule Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 108090000623 proteins and genes Proteins 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 235000015112 vegetable and seed oil Nutrition 0.000 description 3
- ALVKGSGIVCHADB-UHFFFAOYSA-N 1-[bis(2-ethylhexoxy)phosphoryl]octane Chemical compound CCCCCCCCP(=O)(OCC(CC)CCCC)OCC(CC)CCCC ALVKGSGIVCHADB-UHFFFAOYSA-N 0.000 description 2
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 241000209082 Lolium Species 0.000 description 2
- 244000061456 Solanum tuberosum Species 0.000 description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 230000004071 biological effect Effects 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 239000004491 dispersible concentrate Substances 0.000 description 2
- 239000003337 fertilizer Substances 0.000 description 2
- 239000013022 formulation composition Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000011785 micronutrient Substances 0.000 description 2
- 235000013369 micronutrients Nutrition 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 239000000575 pesticide Substances 0.000 description 2
- 231100000614 poison Toxicity 0.000 description 2
- 239000002574 poison Substances 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 239000013589 supplement Substances 0.000 description 2
- DQKWXTIYGWPGOO-UHFFFAOYSA-N (2,6-dibromo-4-cyanophenyl) octanoate Chemical compound CCCCCCCC(=O)OC1=C(Br)C=C(C#N)C=C1Br DQKWXTIYGWPGOO-UHFFFAOYSA-N 0.000 description 1
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- NNHCFSLBNPIGQO-UHFFFAOYSA-N 1,4,5-oxadiazepine Chemical compound O1C=CN=NC=C1 NNHCFSLBNPIGQO-UHFFFAOYSA-N 0.000 description 1
- OSNIIMCBVLBNGS-UHFFFAOYSA-N 1-(1,3-benzodioxol-5-yl)-2-(dimethylamino)propan-1-one Chemical compound CN(C)C(C)C(=O)C1=CC=C2OCOC2=C1 OSNIIMCBVLBNGS-UHFFFAOYSA-N 0.000 description 1
- JPGXOMADPRULAC-UHFFFAOYSA-N 1-[butoxy(butyl)phosphoryl]oxybutane Chemical compound CCCCOP(=O)(CCCC)OCCCC JPGXOMADPRULAC-UHFFFAOYSA-N 0.000 description 1
- NUPJIGQFXCQJBK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-5-(methoxymethyl)nicotinic acid Chemical compound OC(=O)C1=CC(COC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 NUPJIGQFXCQJBK-UHFFFAOYSA-N 0.000 description 1
- MPPOHAUSNPTFAJ-UHFFFAOYSA-N 2-[4-[(6-chloro-1,3-benzoxazol-2-yl)oxy]phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 MPPOHAUSNPTFAJ-UHFFFAOYSA-N 0.000 description 1
- CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical class O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 description 1
- GOCVCBDBQYEFQD-UHFFFAOYSA-N 3-[[2-ethylhexoxy(2-ethylhexyl)phosphoryl]oxymethyl]heptane Chemical compound CCCCC(CC)COP(=O)(CC(CC)CCCC)OCC(CC)CCCC GOCVCBDBQYEFQD-UHFFFAOYSA-N 0.000 description 1
- 108010020183 3-phosphoshikimate 1-carboxyvinyltransferase Proteins 0.000 description 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- MBFHUWCOCCICOK-UHFFFAOYSA-N 4-iodo-2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(I)C=2)C(O)=O)=N1 MBFHUWCOCCICOK-UHFFFAOYSA-N 0.000 description 1
- 241000743985 Alopecurus Species 0.000 description 1
- 241000219318 Amaranthus Species 0.000 description 1
- 241000254175 Anthonomus grandis Species 0.000 description 1
- 241001666377 Apera Species 0.000 description 1
- 235000005781 Avena Nutrition 0.000 description 1
- 244000075850 Avena orientalis Species 0.000 description 1
- 241000193388 Bacillus thuringiensis Species 0.000 description 1
- 235000014698 Brassica juncea var multisecta Nutrition 0.000 description 1
- 240000002791 Brassica napus Species 0.000 description 1
- 235000006008 Brassica napus var napus Nutrition 0.000 description 1
- 235000006618 Brassica rapa subsp oleifera Nutrition 0.000 description 1
- 244000188595 Brassica sinapistrum Species 0.000 description 1
- 241000209200 Bromus Species 0.000 description 1
- 241000219312 Chenopodium Species 0.000 description 1
- 244000192528 Chrysanthemum parthenium Species 0.000 description 1
- 241000207892 Convolvulus Species 0.000 description 1
- 241000254171 Curculionidae Species 0.000 description 1
- 229920005682 EO-PO block copolymer Polymers 0.000 description 1
- 241000192043 Echinochloa Species 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- 239000005566 Imazamox Substances 0.000 description 1
- 239000005568 Iodosulfuron Substances 0.000 description 1
- 241000258916 Leptinotarsa decemlineata Species 0.000 description 1
- 235000017945 Matricaria Nutrition 0.000 description 1
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 1
- 239000005582 Metosulam Substances 0.000 description 1
- VGHPMIFEKOFHHQ-UHFFFAOYSA-N Metosulam Chemical compound N1=C2N=C(OC)C=C(OC)N2N=C1S(=O)(=O)NC1=C(Cl)C=CC(C)=C1Cl VGHPMIFEKOFHHQ-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- 241001147398 Ostrinia nubilalis Species 0.000 description 1
- 241000745991 Phalaris Species 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 239000005596 Picolinafen Substances 0.000 description 1
- 241000209504 Poaceae Species 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 241000205407 Polygonum Species 0.000 description 1
- 229920002396 Polyurea Polymers 0.000 description 1
- 239000005607 Pyroxsulam Substances 0.000 description 1
- DABVLDPIQCWUFQ-UHFFFAOYSA-N S(=O)(=O)(OCCCCCCCCCCCC)[O-].[NH4+].C(C)O.C(C)O Chemical compound S(=O)(=O)(OCCCCCCCCCCCC)[O-].[NH4+].C(C)O.C(C)O DABVLDPIQCWUFQ-UHFFFAOYSA-N 0.000 description 1
- 235000007238 Secale cereale Nutrition 0.000 description 1
- 244000082988 Secale cereale Species 0.000 description 1
- 235000005775 Setaria Nutrition 0.000 description 1
- 241000232088 Setaria <nematode> Species 0.000 description 1
- 241000220261 Sinapis Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 240000006694 Stellaria media Species 0.000 description 1
- 235000019714 Triticale Nutrition 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 235000007264 Triticum durum Nutrition 0.000 description 1
- 241000209143 Triticum turgidum subsp. durum Species 0.000 description 1
- 241000405217 Viola <butterfly> Species 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229940097012 bacillus thuringiensis Drugs 0.000 description 1
- 230000008827 biological function Effects 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000007891 compressed tablet Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 239000002577 cryoprotective agent Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 238000012239 gene modification Methods 0.000 description 1
- 230000005017 genetic modification Effects 0.000 description 1
- 235000013617 genetically modified food Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000011859 microparticle Substances 0.000 description 1
- GLBLPMUBLHYFCW-UHFFFAOYSA-N n-(5,7-dimethoxy-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)-2-methoxy-4-(trifluoromethyl)pyridine-3-sulfonamide Chemical compound N1=C2N=C(OC)C=C(OC)N2N=C1NS(=O)(=O)C1=C(OC)N=CC=C1C(F)(F)F GLBLPMUBLHYFCW-UHFFFAOYSA-N 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- CWKFPEBMTGKLKX-UHFFFAOYSA-N picolinafen Chemical compound C1=CC(F)=CC=C1NC(=O)C1=CC=CC(OC=2C=C(C=CC=2)C(F)(F)F)=N1 CWKFPEBMTGKLKX-UHFFFAOYSA-N 0.000 description 1
- IUGYQRQAERSCNH-UHFFFAOYSA-M pivalate Chemical compound CC(C)(C)C([O-])=O IUGYQRQAERSCNH-UHFFFAOYSA-M 0.000 description 1
- 239000004476 plant protection product Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- 108700012359 toxins Proteins 0.000 description 1
- 230000009261 transgenic effect Effects 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- WVPGXJOLGGFBCR-UHFFFAOYSA-N trioctyl phosphate Chemical compound CCCCCCCCOP(=O)(OCCCCCCCC)OCCCCCCCC WVPGXJOLGGFBCR-UHFFFAOYSA-N 0.000 description 1
- WTLBZVNBAKMVDP-UHFFFAOYSA-N tris(2-butoxyethyl) phosphate Chemical compound CCCCOCCOP(=O)(OCCOCCCC)OCCOCCCC WTLBZVNBAKMVDP-UHFFFAOYSA-N 0.000 description 1
- 241001478887 unidentified soil bacteria Species 0.000 description 1
- 239000002435 venom Substances 0.000 description 1
- 231100000611 venom Toxicity 0.000 description 1
- 210000001048 venom Anatomy 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000004565 water dispersible tablet Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 241000228158 x Triticosecale Species 0.000 description 1
- 239000012991 xanthate Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic 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
- 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
- A01N25/22—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 containing ingredients stabilising the active ingredients
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
ピノキサデンを0.5〜50%、好ましくは2〜20%、最も好ましくは5〜10%、
補助剤を2〜80%、好ましくは10〜60%、最も好ましくは15〜40%、
乳化剤を0.5〜50%、好ましくは2〜30%、より好ましくは2〜10%、
溶媒を0〜90%、好ましくは10〜60%、より好ましくは15〜40%、
水を0〜80%及び
油担体(前記補助剤又は溶媒担体とは異なる)を0〜80%含んでなる。
高性能油状補助剤としてのトリス−(2−エチルヘキシル)ホスフェートの使用は化学的に安定な活性ワンパック製剤の開発を可能にした。本発明による典型的な組成物、ECの形態の組成物A及びB1の安定性を、以下の表1中の他の組み込み補助剤組成物との比較で、以下に概説する。
EC(1)は表1の組成物Aであり、EC(2)は市販の入手可能なアキシャル(Axial)100ECである。
試験植物には、200 L/haスプレー体積を使用してピノキサデン30 g/haでスプレーした。スプレー施用後21日目に目視評価により観察した結果を、以下の表3にまとめた。EC(2)での処置は、200 Lスプレー溶液当たり1Lのナタネ油メチルエステル補助剤をタンク混合補助剤として施用したが、EC(1)での処置は表1の組成物Aを600 mL施用しただけの結果であり、この組成物中のトリス−(2−エチルヘキシル)ホスフェート組み込み補助剤はたったの34%であることに注目すべきである。
Claims (22)
- ピノキサデン及び補助剤を含んでなる液体除草組成物であって、前記補助剤が、トリス−(2−エチルヘキシル)ホスフェートからなる組み込み補助剤である、液体除草組成物。
- 温度50℃で2週間保存後のピノキサデンの分解が2.5%未満である、請求項1に記載の組成物。
- アルキル硫酸の塩、アリールスルホン酸の塩、アルキルフェノール−アルキレンオキシド付加生成物、アルコール−アルキレンオキシド付加生成物、セッケン、アルキルナフタレンスルホン酸の塩、スルホコハク酸塩のジアルキルエステル、ソルビトールエステル、4級アミン、脂肪酸のポリエチレングリコールエステル、エチレンオキシド及びプロピレンオキシドのブロック共重合体、又はこれらの1又は複数の混合物、を含んでなる乳化剤を含む、請求項1又は2に記載の組成物。
- 前記乳化剤が、ジエタノールアンモニウムラウリル硫酸、ドデシルベンゼンスルホン酸カルシウム、ノニルフェノールエトキシレート、トリデシルアルコールエトキシレート、ステアリン酸ナトリウム、ジブチルナフタレンスルホン酸ナトリウム、ジ(2−エチルヘキシル)スルホコハク酸ナトリウム、ソルビトールオレイン酸エステル、ラウリルトリメチルアンモニウムクロライド、ポリエチレングリコールステアリン酸エステル、エチレンオキシド及びプロピレンオキシドのブロック共重合体、又はこれらの乳化剤の1又は複数の混合物を含んでなる、請求項3記載の組成物。
- 前記組成物が、
ピノキサデンを0.5〜50%、
補助剤を10〜80%、
乳化剤を0.5〜50%、
溶媒を10〜90%、
水を0〜80%及び
油担体(前記補助剤又は溶媒担体とは異なる)を0〜80%含んでなる、
請求項1又は2に記載の組成物。 - 前記組成物が、
ピノキサデンを0.5〜50%、
補助剤を10〜60%、
乳化剤を0.5〜50%、
溶媒を10〜60%、
水を0〜80%及び
油担体(前記補助剤又は溶媒担体とは異なる)を0〜80%含んでなる、
請求項5記載の組成物。 - 前記組成物が、
ピノキサデンを2〜20%、
補助剤を10〜60%、
乳化剤を2〜30%、
溶媒を10〜60%、
水を0〜80%及び
油担体(前記補助剤又は溶媒担体とは異なる)を0〜80%含んでなる、
請求項6記載の組成物。 - 前記乳化剤が、アルキル硫酸の塩、アリールスルホン酸の塩、アルキルフェノール−アルキレンオキシド付加生成物、アルコール−アルキレンオキシド付加生成物、セッケン、アルキルナフタレンスルホン酸の塩、スルホコハク酸塩のジアルキルエステル、ソルビトールエステル、4級アミン、脂肪酸のポリエチレングリコールエステル、又は1又は複数のこれら物質の組み合わせである、請求項5〜7のいずれか1項に記載の組成物。
- 前記溶媒が、重質芳香族炭化水素混合物;又は2−エチルヘキサノール、n−オクタノール、テトラヒドロフルフリルアルコール、2−メチル−2,4−ペンタンジオール、4−ヒドロキシ−4−メチル−2−ペンタノン、乳酸メチルエステル、乳酸ブチルエステル、シクロヘキサノール、ベンジルアルコール、ベンジルベンゾエート、及びベンジルラクテート、又は1又は複数のこれら物質の混合物からなる群から選択されるアルコール又はアルコールの誘導体である、請求項5〜7のいずれか1項に記載の組成物。
- 前記溶媒が、テトラヒドロフルフリルアルコール、ベンジルアルコール又は2−メチル−2,4−ペンタンジオールである、請求項9記載の組成物。
- 前記溶媒が、テトラヒドロフルフリルアルコールである、請求項10記載の組成物。
- 重質芳香族炭化水素混合物;又は2−エチルヘキサノール、n−オクタノール、テトラヒドロフルフリルアルコール、2−メチル−2,4−ペンタンジオール、4−ヒドロキシ−4−メチル−2−ペンタノン、乳酸メチルエステル、乳酸ブチルエステル、シクロヘキサノール、ベンジルアルコール、ベンジルベンゾエート、及びベンジルラクテート、からなる群から選択される、1又は複数のアルコール又はアルコールの誘導体、を含んでなる溶媒を含む、請求項1又は2に記載の組成物。
- 前記溶媒が、テトラヒドロフルフリルアルコール、ベンジルアルコール及び2−メチル−2,4−ペンタンジオールを含んでなる、請求項12記載の組成物。
- 前記溶媒が、テトラヒドロフルフリルアルコールを含んでなる、請求項13記載の組成物。
- 薬害軽減剤(safener)を含んでなる、請求項1又は2に記載の組成物。
- 前記薬害軽減剤が、クロキントセット−メチル(cloquintocet-mexyl)、メフェンピル−ジエチル(mefenpyr-diethyl)、及びイソキサジフェン−エチル(isoxadifen-ethyl)からなる群から選択される、請求項15記載の組成物。
- 前記組成物が、アリールオキシ及びへテロアリールオキシフェノキシプロピオン酸、シクロヘキサンジオン、スルホニルウレア、トリアゾロピリミジン、ニトリル、チオカルバメート、ジニトロアニリン、安息香酸、フェノキシ酸及びピリジンカルボン酸からなる群から選択される共除草剤(co-herbicide)を含んでなる、請求項1又は2に記載の組成物。
- 前記組成物が、クロジナホプ(clodinafop)、トラルコキシジム(tralkoxydim)、プロスルホカルブ(prosulfocarb)、トリアスルフロン(triasulfuron)、プロスルフロン(prosulfuron)、アミドスルフロン(amidosulfuron)、クロルスルフロン(chlorsulfuron)、フルピルスルフロン(flupyrsulfuron)、メソスルフロン(mesosulfuron)、メトスルフロン(metsulfuron)、スルホスルフロン(sulfosulfuron)、チフェンスルフロン(thifensulfuron)、トリベヌロン(tribenuron)、トリトスルフロン(tritosulfuron)、フロラスラム(florasulam)、メトスラム(metosulam)、フルメトスラム(flumetsulam)、2,4-D、2,4-DP、ジクロルプロップ−p(dichlorprop-p)、MCPA、メコプロップ(mecoprop)、メコプロップ−p(mecoprop-p)、MCPB、クロピラリド(clopyralid)、ブロモキシニル(bromoxynil)、ブロモキシニル−オクタノエート(bromoxynil-octanoate)、イオキシニル(ioxynil)、イオキシニル−オクタノエート(ioxynil-octanoate)、フルロキシピル(fluroxypyr)、トリフルラリン(trifluralin)、ジフルフェニカン(diflufenican)、ペンジメタリン(pendimethalin)又はトリアレート(triallate)を含んでなる、請求項17記載の組成物。
- 前記組成物が、トラルコキシジム、トリアスルフロン、フロラスラム、クロジナホップ又はクロジナホップとクロキントセットの組み合わせを含んでなる、請求項18記載の組成物。
- 前記組成物が、乳化濃縮剤(EC)、油分散剤(OD)、サスポエマルション(suspo-emulsion、SE)又は水中エマルション(EW)の形態である、請求項1〜19のいずれか1項に記載の組成物。
- 不所望の植物生育の阻害又は制御のための方法であって、請求項1〜20のいずれか1項に記載の組成物の除草有効量を前記植物又はその生息場所に施用する方法。
- 前記組成物が、穀類の作物に使用される、請求項21記載の方法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0621440.7A GB0621440D0 (en) | 2006-10-27 | 2006-10-27 | Herbicidal compositions |
GB0621440.7 | 2006-10-27 | ||
PCT/EP2007/009276 WO2008049618A2 (en) | 2006-10-27 | 2007-10-25 | Herbicidal compositions |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2010507611A JP2010507611A (ja) | 2010-03-11 |
JP2010507611A5 JP2010507611A5 (ja) | 2010-12-16 |
JP5363328B2 true JP5363328B2 (ja) | 2013-12-11 |
Family
ID=37546114
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2009533734A Active JP5363328B2 (ja) | 2006-10-27 | 2007-10-25 | 除草組成物 |
Country Status (33)
Country | Link |
---|---|
US (1) | US9414593B2 (ja) |
EP (1) | EP2079310B1 (ja) |
JP (1) | JP5363328B2 (ja) |
KR (1) | KR101494629B1 (ja) |
CN (1) | CN101562978B (ja) |
AP (1) | AP3424A (ja) |
AR (1) | AR063370A1 (ja) |
AU (1) | AU2007308353B2 (ja) |
BR (1) | BRPI0718023B1 (ja) |
CA (2) | CA2857853A1 (ja) |
CL (1) | CL2007003078A1 (ja) |
CY (1) | CY1119699T1 (ja) |
EA (1) | EA016230B1 (ja) |
EG (1) | EG25546A (ja) |
ES (1) | ES2646994T3 (ja) |
GB (1) | GB0621440D0 (ja) |
GE (1) | GEP20125372B (ja) |
HR (1) | HRP20171571T1 (ja) |
HU (1) | HUE037248T2 (ja) |
IL (1) | IL198242A (ja) |
LT (1) | LT2079310T (ja) |
MA (1) | MA30804B1 (ja) |
ME (1) | ME00787B (ja) |
MX (1) | MX2009004245A (ja) |
NZ (1) | NZ576161A (ja) |
PL (1) | PL2079310T3 (ja) |
PT (1) | PT2079310T (ja) |
SA (1) | SA07280494B1 (ja) |
SI (1) | SI2079310T1 (ja) |
TN (1) | TN2009000156A1 (ja) |
UA (1) | UA93926C2 (ja) |
WO (1) | WO2008049618A2 (ja) |
ZA (1) | ZA200902728B (ja) |
Families Citing this family (47)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2095710A1 (de) * | 2008-02-27 | 2009-09-02 | Bayer CropScience AG | Herbizid-Kombinationen enthaltend Diflufenican |
AR081735A1 (es) | 2010-03-05 | 2012-10-17 | Syngenta Ltd | Composicion herbicida que comprende, como ingrediente activo, una mezcla de pinoxaden y un herbicida adicional |
FR2967361A1 (fr) * | 2010-11-16 | 2012-05-18 | Rhodia Operations | Dispersions huileuses de composes solides contenant des esters de phosphate |
EA023452B1 (ru) | 2011-02-11 | 2016-06-30 | Басф Се | Гербицидные композиции, содержащие топрамезон, пиноксаден и клохинтоцет |
CA2835187A1 (en) * | 2011-05-06 | 2012-11-15 | Syngenta Participations Ag | Herbicidal composition comprising pinoxaden and fluroxypyr, and methods of use thereof |
CN102283217B (zh) * | 2011-06-27 | 2014-08-13 | 陕西美邦农药有限公司 | 一种含双氟磺草胺与唑啉草酯的除草组合物 |
CN102283220A (zh) * | 2011-07-04 | 2011-12-21 | 永农生物科学有限公司 | 氯氟吡氧乙酸或其酯和唑嘧磺草胺的组合物及其制备方法 |
GB201115564D0 (en) | 2011-09-08 | 2011-10-26 | Syngenta Ltd | Herbicidal composition |
GB201121377D0 (en) * | 2011-12-12 | 2012-01-25 | Syngenta Ltd | Formulation component |
CN103238597A (zh) * | 2012-02-10 | 2013-08-14 | 中国中化股份有限公司 | 肟草酮组合物 |
AU2013333884B2 (en) | 2012-10-19 | 2016-10-13 | Syngenta Participations Ag | Liquid agrochemical compositions comprising a polymeric thickener and an alcohol-containing solvent system, and liquid herbicidal compositions having an alcohol-containing solvent system |
CN102907443B (zh) * | 2012-10-31 | 2014-02-12 | 青岛瀚生生物科技股份有限公司 | 农用田间除草剂 |
CN103355337B (zh) * | 2013-07-31 | 2015-03-18 | 联保作物科技有限公司 | 一种麦田除草组合物及其制剂 |
CN103461364A (zh) * | 2013-08-20 | 2013-12-25 | 湖南农大海特农化有限公司 | 含有甲基二磺隆和唑啉草酯的除草组合物 |
CN103493837A (zh) * | 2013-09-12 | 2014-01-08 | 薛列驹 | 一种水稻田复配除草剂 |
FR3013044A1 (fr) * | 2013-11-13 | 2015-05-15 | Rhodia Operations | Dopes d'adhesivite liquides pour enrobes bitumineux |
UY35923A (es) * | 2013-12-30 | 2015-07-31 | Rhodia Operations | ?composiciones pesticidas agrícolas?. |
CN103783050B (zh) * | 2014-01-21 | 2016-04-13 | 山东滨农科技有限公司 | 一种唑啉草酯水分散粒剂及其制备方法 |
CN103918689B (zh) * | 2014-03-27 | 2016-09-14 | 广东中迅农科股份有限公司 | 一种含有噻吩磺隆和辛酰溴苯腈的除草组合物 |
US10173943B2 (en) | 2015-05-11 | 2019-01-08 | Dow Agrosciences, Llc | Non-corrosive nitrification inhibitor polar solvent formulation |
CN104982450A (zh) * | 2015-07-10 | 2015-10-21 | 广东中迅农科股份有限公司 | 含有甲基二磺隆和唑啉草酯以及双氟磺草胺的农药组合物 |
CN105104404B (zh) * | 2015-09-24 | 2017-09-29 | 山东潍坊润丰化工股份有限公司 | 一种噻吩磺隆与唑啉草酯的除草组合物及其应用 |
CA3002528A1 (en) * | 2015-10-22 | 2017-04-27 | Hiteshkumar Dave | Non-corrosive nitrification inhibitor polar solvent formulation |
CN106332874A (zh) * | 2016-08-25 | 2017-01-18 | 安徽美兰农业发展股份有限公司 | 一种唑啉草酯和氯氟吡氧乙酸异辛酯复配乳油及其制备方法 |
CN106332875A (zh) * | 2016-08-25 | 2017-01-18 | 安徽美兰农业发展股份有限公司 | 一种唑啉草酯和辛酰溴苯腈复配乳油及其制备方法 |
CN106489958A (zh) * | 2016-09-28 | 2017-03-15 | 安徽众邦生物工程有限公司 | 一种含精噁唑禾草灵和唑啉草酯的除草组合物 |
GB201707930D0 (en) * | 2017-05-17 | 2017-06-28 | Syngenta Participations Ag | Formulation component |
CN109287625A (zh) * | 2018-11-28 | 2019-02-01 | 浙江中山化工集团股份有限公司 | 一种双氟磺草胺和唑啉草酯复配乳油及其制备方法 |
CN109329292A (zh) * | 2018-12-18 | 2019-02-15 | 上海祥霖农业技术有限公司 | 一种唑啉草酯和氯氟吡氧乙酸的可分散油悬浮剂及其制备方法和应用 |
WO2020199078A1 (zh) | 2019-04-01 | 2020-10-08 | 泸州东方农化有限公司 | 一种卤代共轭二烯类化合物及其制备和应用 |
AU2019438654B2 (en) | 2019-04-01 | 2022-10-20 | Oriental (Luzhou) Agrochemicals Co., Ltd. | Conjugated triene compound, preparation method therefor and use thereof |
BR112021024263A2 (pt) * | 2019-06-03 | 2022-01-11 | Bayer Ag | Combinações adjuvantes como aceleradores de absorção foliar para composições herbicidas |
EP4159039A1 (en) | 2019-07-18 | 2023-04-05 | Adama Agan Ltd. | Stable formulation comprising pinoxaden |
CN110402923A (zh) * | 2019-08-16 | 2019-11-05 | 山西农业大学 | 唑啉草酯水乳剂及其制备方法和应用 |
CN111226962A (zh) * | 2020-02-21 | 2020-06-05 | 安徽丰乐农化有限责任公司 | 一种大麦田苗后复配除草剂 |
CN111296464A (zh) * | 2020-03-19 | 2020-06-19 | 利尔化学股份有限公司 | 一种含有唑啉草酯的除草组合物 |
EP4132937A1 (en) | 2020-04-06 | 2023-02-15 | Adama Agan Ltd. | Co-crystals of antioxidants and active ingredients and use of antioxidants as stabilizer |
WO2022117515A1 (en) | 2020-12-01 | 2022-06-09 | Bayer Aktiengesellschaft | Compositions comprising iodosulfuron-methyl and tehp |
EP4255188A1 (en) | 2020-12-01 | 2023-10-11 | Bayer Aktiengesellschaft | Compositions comprising mesosulfuron-methyl and tehp |
CN117119890A (zh) * | 2021-03-30 | 2023-11-24 | 斯泰潘公司 | 农用制剂 |
CN115590028B (zh) * | 2021-06-28 | 2024-12-06 | 迈克斯(如东)化工有限公司 | 除草剂组合物及其制备方法和施用方法 |
GB202117595D0 (en) * | 2021-12-06 | 2022-01-19 | Syngenta Crop Protection Ag | Herbicidal compositions |
GB202117598D0 (en) | 2021-12-06 | 2022-01-19 | Syngenta Crop Protection Ag | Herbicidal compositions |
GB202117597D0 (en) * | 2021-12-06 | 2022-01-19 | Syngenta Crop Protection Ag | Herbicidal compositions |
WO2024083558A1 (en) * | 2022-10-17 | 2024-04-25 | Syngenta Crop Protection Ag | Emulsifiable concentrate (ec) |
WO2024217654A1 (ru) * | 2023-04-20 | 2024-10-24 | Акционерное общество Фирма "Август" | Жидкая гербицидная композиция и соединения для ее стабилизации |
WO2025012778A1 (en) * | 2023-07-07 | 2025-01-16 | Savi Bhutani | Synergistic herbicidal composition and process thereof |
Family Cites Families (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9118565D0 (en) | 1991-08-30 | 1991-10-16 | Schering Ag | Herbicidal compositions |
DE4319263A1 (de) | 1992-07-03 | 1994-01-05 | Schoenherr Joerg | Pflanzenbehandlungsmittel |
DE4305542C1 (de) * | 1993-02-20 | 1994-07-21 | Schering Ag | Herbizide Mittel mit synergistischer Wirkung |
DK0655197T3 (da) * | 1993-11-16 | 1999-02-01 | Bayer Ag | Anvendelse af phosphorsyreestere som krystallisationsinhibitorer |
GB9500983D0 (en) | 1995-01-19 | 1995-03-08 | Agrevo Uk Ltd | Pesticidal compositions |
GB9613637D0 (en) | 1996-06-28 | 1996-08-28 | Agrevo Uk Ltd | Fungicidal compositions |
AR015243A1 (es) * | 1998-03-13 | 2001-04-18 | Syngenta Participations AG | Derivados de 3-hidroxi-4-aril-5-oxopirazolino, composicion herbicida e inhibidora del crecimiento de las plantas y metodo para controlar el crecimiento de las plantas. |
DE19913036A1 (de) * | 1999-03-23 | 2000-09-28 | Aventis Cropscience Gmbh | Flüssige Zubereitungen und Tensid/Lösungsmittel-Systeme |
RU2251268C9 (ru) | 1999-09-07 | 2012-12-20 | Зингента Партисипейшнс Аг | Гербицидная композиция, способ избирательной борьбы с сорными и травянистыми растениями |
ES2216957T3 (es) | 1999-09-07 | 2004-11-01 | Syngenta Participations Ag | Medio herbicida. |
HU229958B1 (hu) | 1999-09-07 | 2015-03-30 | Syngenta Participations Ag | Herbicid vegyületek, ezeket tartalmazó készítmények, eljárás a vegyületek előállítására, valamint eljárás gyomnövények irtására |
PL199182B1 (pl) | 1999-09-07 | 2008-08-29 | Syngenta Participations Ag | Kompozycja selektywna herbicydowo oraz sposób selektywnego zwalczania chwastów i traw w uprawach roślin użytkowych |
DE19963381A1 (de) * | 1999-12-28 | 2001-07-12 | Aventis Cropscience Gmbh | Tensid/Lösungsmittel-Systeme |
DE60014175T2 (de) | 2000-01-26 | 2005-10-06 | Nokia Corp. | Verfahren und vorrichtung zum kompensieren von nicht-linearitäten und zeitvarianten änderungen einer übertragungsfunktion wirksam auf ein eingangssignal |
CA2447897A1 (en) | 2001-05-21 | 2002-12-27 | Monsanto Technology Llc | Pesticide concentrates containing etheramine surfactants |
GB0121580D0 (en) * | 2001-09-06 | 2001-10-24 | Syngenta Ltd | Novel compounds |
PL207276B1 (pl) | 2001-09-27 | 2010-11-30 | Syngenta Participations Ag | Kompozycja chwastobójcza oraz sposób selektywnego zwalczania chwastów i traw w uprawach roślin użytkowych |
GB0126144D0 (en) * | 2001-10-31 | 2002-01-02 | Syngenta Ltd | Pesticidal formulations |
GB0211924D0 (en) | 2002-05-23 | 2002-07-03 | Syngenta Ltd | Composition |
GB0213654D0 (en) | 2002-06-13 | 2002-07-24 | Syngenta Ltd | Composition |
GB0213638D0 (en) | 2002-06-13 | 2002-07-24 | Syngenta Ltd | Composition |
DE102004047092A1 (de) * | 2004-09-29 | 2006-03-30 | Clariant Gmbh | Agrochemische Zusammensetzung enthaltend Phosphorsäureester |
TW200621157A (en) | 2004-12-06 | 2006-07-01 | Syngenta Participations Ag | Herbicidal composition |
SA06270491B1 (ar) | 2005-12-27 | 2010-10-20 | سينجنتا بارتيسبيشنز ايه جي | تركيبة مبيدة للأعشاب تشتمل على حمض 2، 2- ثنائي ميثيل بروبيونيك 8- (2، 6- ثنائي إيثيل –4- ميثيل – فينيل) –9- أوكسو –1، 2، 4، 5- تتراهيدرو –9h- بيرازولو[2.1-دي][ 5.4.1] أوكسادايازيبين –7- يل إستر وكحول |
EP2114149A2 (en) | 2007-01-29 | 2009-11-11 | Syngeta Participations AG | Herbicidal composition |
RU2337545C1 (ru) | 2007-04-18 | 2008-11-10 | Закрытое акционерное общество Фирма "Август" | Гербицидная композиция и способ борьбы с нежелательной растительностью |
-
2006
- 2006-10-27 GB GBGB0621440.7A patent/GB0621440D0/en not_active Ceased
-
2007
- 2007-09-15 SA SA07280494A patent/SA07280494B1/ar unknown
- 2007-10-24 AR ARP070104702A patent/AR063370A1/es active IP Right Grant
- 2007-10-25 US US12/447,269 patent/US9414593B2/en active Active
- 2007-10-25 KR KR1020097008666A patent/KR101494629B1/ko active IP Right Grant
- 2007-10-25 MX MX2009004245A patent/MX2009004245A/es active IP Right Grant
- 2007-10-25 SI SI200731982T patent/SI2079310T1/sl unknown
- 2007-10-25 EP EP07819325.7A patent/EP2079310B1/en active Active
- 2007-10-25 UA UAA200904730A patent/UA93926C2/ru unknown
- 2007-10-25 BR BRPI0718023-3A2 patent/BRPI0718023B1/pt active IP Right Grant
- 2007-10-25 AP AP2009004838A patent/AP3424A/xx active
- 2007-10-25 ES ES07819325.7T patent/ES2646994T3/es active Active
- 2007-10-25 ME MEP-2009-134A patent/ME00787B/me unknown
- 2007-10-25 LT LTEP07819325.7T patent/LT2079310T/lt unknown
- 2007-10-25 WO PCT/EP2007/009276 patent/WO2008049618A2/en active Application Filing
- 2007-10-25 PT PT78193257T patent/PT2079310T/pt unknown
- 2007-10-25 CN CN200780039997.XA patent/CN101562978B/zh active Active
- 2007-10-25 AU AU2007308353A patent/AU2007308353B2/en active Active
- 2007-10-25 CA CA2857853A patent/CA2857853A1/en not_active Abandoned
- 2007-10-25 HU HUE07819325A patent/HUE037248T2/hu unknown
- 2007-10-25 PL PL07819325T patent/PL2079310T3/pl unknown
- 2007-10-25 NZ NZ576161A patent/NZ576161A/en unknown
- 2007-10-25 GE GEAP200711272A patent/GEP20125372B/en unknown
- 2007-10-25 EA EA200900553A patent/EA016230B1/ru not_active IP Right Cessation
- 2007-10-25 CA CA2667408A patent/CA2667408C/en active Active
- 2007-10-25 JP JP2009533734A patent/JP5363328B2/ja active Active
- 2007-10-25 CL CL2007003078A patent/CL2007003078A1/es unknown
-
2009
- 2009-04-20 ZA ZA200902728A patent/ZA200902728B/xx unknown
- 2009-04-20 IL IL198242A patent/IL198242A/en active IP Right Grant
- 2009-04-22 MA MA31806A patent/MA30804B1/fr unknown
- 2009-04-22 EG EG2009040551A patent/EG25546A/xx active
- 2009-04-24 TN TNP2009000156A patent/TN2009000156A1/fr unknown
-
2017
- 2017-10-16 HR HRP20171571TT patent/HRP20171571T1/hr unknown
- 2017-11-08 CY CY20171101167T patent/CY1119699T1/el unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5363328B2 (ja) | 除草組成物 | |
US10512264B2 (en) | Herbicidal mixtures | |
WO2009012979A2 (en) | Herbicidal compositions comprising pyroxsulam and a fatty acid alkyl ester | |
RU2650393C2 (ru) | Синергетическая борьба с сорняками путем нанесения фенокссулама и бензобициклона или кломазона и бензобициклона | |
TW200920257A (en) | Herbicide combinations comprising specific 3-(2-alkoxy-4-chloro-6-alkylphenyl)-substituted tetramates | |
KR20140006884A (ko) | 페녹스술람, 트리클로피르 및 이마제타피르 또는 이마자목스를 함유하는 상승작용성 제초제 조성물 | |
CA2781062A1 (en) | Synergistic herbicidal compositions containing benfluralin | |
KR102687204B1 (ko) | 피록스술람 조성물의 완화를 위한 클로퀸토세트 염 | |
US20250031701A1 (en) | Herbicidal Compositions | |
US20250024839A1 (en) | Herbicidal Compositions | |
EP4444093A1 (en) | Herbicidal compositions | |
WO2024175475A1 (en) | Herbicidal compositions |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20101025 |
|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20101025 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20121017 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20121023 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20130122 |
|
A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20130129 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20130423 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20130806 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20130905 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 5363328 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |