TW200306153A - Granular agricultural-chemical composition - Google Patents
Granular agricultural-chemical composition Download PDFInfo
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- TW200306153A TW200306153A TW092106985A TW92106985A TW200306153A TW 200306153 A TW200306153 A TW 200306153A TW 092106985 A TW092106985 A TW 092106985A TW 92106985 A TW92106985 A TW 92106985A TW 200306153 A TW200306153 A TW 200306153A
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- Prior art keywords
- parts
- water
- pesticide composition
- mass
- granular pesticide
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- 239000000203 mixture Substances 0.000 title claims abstract description 172
- 239000003905 agrochemical Substances 0.000 title abstract description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 136
- 239000007900 aqueous suspension Substances 0.000 claims abstract description 62
- 239000004480 active ingredient Substances 0.000 claims abstract description 49
- 230000002378 acidificating effect Effects 0.000 claims abstract description 20
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 17
- 239000000126 substance Substances 0.000 claims abstract description 16
- 239000003093 cationic surfactant Substances 0.000 claims abstract description 6
- 239000000575 pesticide Substances 0.000 claims description 176
- 239000008187 granular material Substances 0.000 claims description 57
- -1 sulfonylurea compound Chemical class 0.000 claims description 49
- 239000004009 herbicide Substances 0.000 claims description 11
- 150000003839 salts Chemical class 0.000 claims description 9
- 229940100389 Sulfonylurea Drugs 0.000 claims description 6
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 6
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 3
- 230000000694 effects Effects 0.000 claims description 3
- 239000008202 granule composition Substances 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 125000002490 anilino group Chemical class [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 125000000129 anionic group Chemical group 0.000 claims 1
- 231100000674 Phytotoxicity Toxicity 0.000 abstract description 3
- 238000009472 formulation Methods 0.000 abstract description 2
- 239000000499 gel Substances 0.000 abstract 1
- 230000001105 regulatory effect Effects 0.000 abstract 1
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 58
- 230000000052 comparative effect Effects 0.000 description 53
- 239000002245 particle Substances 0.000 description 46
- 229940126062 Compound A Drugs 0.000 description 43
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 43
- 239000005472 Bensulfuron methyl Substances 0.000 description 37
- XMQFTWRPUQYINF-UHFFFAOYSA-N bensulfuron-methyl Chemical group COC(=O)C1=CC=CC=C1CS(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 XMQFTWRPUQYINF-UHFFFAOYSA-N 0.000 description 37
- 150000001875 compounds Chemical class 0.000 description 35
- 229910000019 calcium carbonate Inorganic materials 0.000 description 29
- 239000004927 clay Substances 0.000 description 28
- 239000000843 powder Substances 0.000 description 27
- 238000004090 dissolution Methods 0.000 description 22
- 229920002472 Starch Polymers 0.000 description 20
- 239000008107 starch Substances 0.000 description 19
- 238000004898 kneading Methods 0.000 description 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 14
- 239000002585 base Substances 0.000 description 14
- 238000012360 testing method Methods 0.000 description 14
- 239000003945 anionic surfactant Substances 0.000 description 13
- WLCFKPHMRNPAFZ-UHFFFAOYSA-M didodecyl(dimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCC WLCFKPHMRNPAFZ-UHFFFAOYSA-M 0.000 description 12
- 239000000047 product Substances 0.000 description 11
- 235000019698 starch Nutrition 0.000 description 11
- 238000000034 method Methods 0.000 description 10
- 229920003023 plastic Polymers 0.000 description 10
- 239000004033 plastic Substances 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 9
- 239000004664 distearyldimethylammonium chloride (DHTDMAC) Substances 0.000 description 9
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 8
- 239000006229 carbon black Substances 0.000 description 8
- 239000005567 Imazosulfuron Substances 0.000 description 7
- 241000209094 Oryza Species 0.000 description 7
- 239000004372 Polyvinyl alcohol Substances 0.000 description 7
- AWZOLILCOUMRDG-UHFFFAOYSA-N edifenphos Chemical compound C=1C=CC=CC=1SP(=O)(OCC)SC1=CC=CC=C1 AWZOLILCOUMRDG-UHFFFAOYSA-N 0.000 description 7
- 238000005469 granulation Methods 0.000 description 7
- 230000003179 granulation Effects 0.000 description 7
- 239000004615 ingredient Substances 0.000 description 7
- 229920002451 polyvinyl alcohol Polymers 0.000 description 7
- 239000002244 precipitate Substances 0.000 description 7
- 229910052708 sodium Inorganic materials 0.000 description 7
- 239000011734 sodium Substances 0.000 description 7
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 7
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 6
- NAGRVUXEKKZNHT-UHFFFAOYSA-N Imazosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N3C=CC=CC3=NC=2Cl)=N1 NAGRVUXEKKZNHT-UHFFFAOYSA-N 0.000 description 6
- 235000007164 Oryza sativa Nutrition 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 6
- 239000008233 hard water Substances 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- 235000009566 rice Nutrition 0.000 description 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 5
- 239000004202 carbamide Substances 0.000 description 5
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- 238000013268 sustained release Methods 0.000 description 5
- 239000012730 sustained-release form Substances 0.000 description 5
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- 229920001353 Dextrin Polymers 0.000 description 4
- 239000004375 Dextrin Substances 0.000 description 4
- 239000004606 Fillers/Extenders Substances 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 235000019270 ammonium chloride Nutrition 0.000 description 4
- 235000019425 dextrin Nutrition 0.000 description 4
- UAKOZKUVZRMOFN-JDVCJPALSA-M dimethyl-bis[(z)-octadec-9-enyl]azanium;chloride Chemical compound [Cl-].CCCCCCCC\C=C/CCCCCCCC[N+](C)(C)CCCCCCCC\C=C/CCCCCCCC UAKOZKUVZRMOFN-JDVCJPALSA-M 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 238000004128 high performance liquid chromatography Methods 0.000 description 4
- 239000002917 insecticide Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000002689 soil Substances 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 3
- 241000254158 Lampyridae Species 0.000 description 3
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 3
- 244000046052 Phaseolus vulgaris Species 0.000 description 3
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 3
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 3
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 3
- ONCZQWJXONKSMM-UHFFFAOYSA-N dialuminum;disodium;oxygen(2-);silicon(4+);hydrate Chemical compound O.[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Na+].[Na+].[Al+3].[Al+3].[Si+4].[Si+4].[Si+4].[Si+4] ONCZQWJXONKSMM-UHFFFAOYSA-N 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 3
- 229940080314 sodium bentonite Drugs 0.000 description 3
- 229910000280 sodium bentonite Inorganic materials 0.000 description 3
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 3
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 3
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 description 3
- 239000013589 supplement Substances 0.000 description 3
- QNLZIZAQLLYXTC-UHFFFAOYSA-N 1,2-dimethylnaphthalene Chemical compound C1=CC=CC2=C(C)C(C)=CC=C21 QNLZIZAQLLYXTC-UHFFFAOYSA-N 0.000 description 2
- 125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- UWVKRNOCDUPIDM-UHFFFAOYSA-N Ethoxysulfuron Chemical compound CCOC1=CC=CC=C1OS(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 UWVKRNOCDUPIDM-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- HWATZEJQIXKWQS-UHFFFAOYSA-N Flazasulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CN=2)C(F)(F)F)=N1 HWATZEJQIXKWQS-UHFFFAOYSA-N 0.000 description 2
- FMGZEUWROYGLAY-UHFFFAOYSA-N Halosulfuron-methyl Chemical compound ClC1=NN(C)C(S(=O)(=O)NC(=O)NC=2N=C(OC)C=C(OC)N=2)=C1C(=O)OC FMGZEUWROYGLAY-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000012872 agrochemical composition Substances 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 150000001448 anilines Chemical class 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- 229940092782 bentonite Drugs 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- 230000004071 biological effect Effects 0.000 description 2
- 239000003738 black carbon Substances 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- RWRIWBAIICGTTQ-UHFFFAOYSA-N difluoromethane Chemical compound FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 description 2
- VFNGKCDDZUSWLR-UHFFFAOYSA-N disulfuric acid Chemical compound OS(=O)(=O)OS(O)(=O)=O VFNGKCDDZUSWLR-UHFFFAOYSA-N 0.000 description 2
- TWFQJFPTTMIETC-UHFFFAOYSA-N dodecan-1-amine;hydron;chloride Chemical compound [Cl-].CCCCCCCCCCCC[NH3+] TWFQJFPTTMIETC-UHFFFAOYSA-N 0.000 description 2
- PGQAXGHQYGXVDC-UHFFFAOYSA-N dodecyl(dimethyl)azanium;chloride Chemical compound Cl.CCCCCCCCCCCCN(C)C PGQAXGHQYGXVDC-UHFFFAOYSA-N 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 238000004811 liquid chromatography Methods 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- NQMRYBIKMRVZLB-UHFFFAOYSA-N methylamine hydrochloride Chemical compound [Cl-].[NH3+]C NQMRYBIKMRVZLB-UHFFFAOYSA-N 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- AQIXEPGDORPWBJ-UHFFFAOYSA-N pentan-3-ol Chemical compound CCC(O)CC AQIXEPGDORPWBJ-UHFFFAOYSA-N 0.000 description 2
- 239000003090 pesticide formulation Substances 0.000 description 2
- 239000005648 plant growth regulator Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- YNWVFADWVLCOPU-MDWZMJQESA-N (1E)-1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol Chemical compound C1=NC=NN1/C(C(O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1 YNWVFADWVLCOPU-MDWZMJQESA-N 0.000 description 1
- DSCUXSOFNVAWPZ-UHFFFAOYSA-N (3-chloropyridin-2-yl)oxy-dihydroxy-sulfanylidene-lambda5-phosphane Chemical compound OP(O)(=S)OC1=NC=CC=C1Cl DSCUXSOFNVAWPZ-UHFFFAOYSA-N 0.000 description 1
- KKMWAPWLGBMQCO-KSBRXOFISA-L (z)-but-2-enedioate;2-hydroxyethyl(trimethyl)azanium Chemical compound C[N+](C)(C)CCO.C[N+](C)(C)CCO.[O-]C(=O)\C=C/C([O-])=O KKMWAPWLGBMQCO-KSBRXOFISA-L 0.000 description 1
- FHGWEHGZBUBQKL-UHFFFAOYSA-N 1,2-benzothiazepine Chemical compound S1N=CC=CC2=CC=CC=C12 FHGWEHGZBUBQKL-UHFFFAOYSA-N 0.000 description 1
- 125000004317 1,3,5-triazin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=N1 0.000 description 1
- ZPQOPVIELGIULI-UHFFFAOYSA-N 1,3-dichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1 ZPQOPVIELGIULI-UHFFFAOYSA-N 0.000 description 1
- VHVMXWZXFBOANQ-UHFFFAOYSA-N 1-Penten-3-ol Chemical compound CCC(O)C=C VHVMXWZXFBOANQ-UHFFFAOYSA-N 0.000 description 1
- RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 description 1
- RAXXELZNTBOGNW-UHFFFAOYSA-N 1H-imidazole Chemical compound C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 1
- PMZDQRJGMBOQBF-UHFFFAOYSA-N 1H-quinolin-4-one Natural products C1=CC=C2C(O)=CC=NC2=C1 PMZDQRJGMBOQBF-UHFFFAOYSA-N 0.000 description 1
- LDXJRKWFNNFDSA-UHFFFAOYSA-N 2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound C1CN(CC2=NNN=C21)CC(=O)N3CCN(CC3)C4=CN=C(N=C4)NCC5=CC(=CC=C5)OC(F)(F)F LDXJRKWFNNFDSA-UHFFFAOYSA-N 0.000 description 1
- DQIOGQHCNLVTSU-UHFFFAOYSA-N 2-[4-[(2,4-dichlorophenyl)methyl]-2,5-dimethylpyrazol-3-yl]oxy-1-phenylethanone Chemical compound C=1C=C(Cl)C=C(Cl)C=1CC=1C(C)=NN(C)C=1OCC(=O)C1=CC=CC=C1 DQIOGQHCNLVTSU-UHFFFAOYSA-N 0.000 description 1
- JVKRKMWZYMKVTQ-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]pyrazol-1-yl]-N-(2-oxo-3H-1,3-benzoxazol-6-yl)acetamide Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C=1C=NN(C=1)CC(=O)NC1=CC2=C(NC(O2)=O)C=C1 JVKRKMWZYMKVTQ-UHFFFAOYSA-N 0.000 description 1
- OCVXSFKKWXMYPF-UHFFFAOYSA-N 2-chloroimidazole Chemical compound ClC1=NC=CN1 OCVXSFKKWXMYPF-UHFFFAOYSA-N 0.000 description 1
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 description 1
- QOLLYDAQOZBRAL-UHFFFAOYSA-M 2-hydroxyethyl-dimethyl-octadecylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCO QOLLYDAQOZBRAL-UHFFFAOYSA-M 0.000 description 1
- 125000005979 2-naphthyloxy group Chemical group 0.000 description 1
- AREOKSGFWPUZLH-UHFFFAOYSA-N 2-propan-2-ylpyrimidin-4-amine Chemical compound CC(C)C1=NC=CC(N)=N1 AREOKSGFWPUZLH-UHFFFAOYSA-N 0.000 description 1
- GPWHFPWZAPOYNO-UHFFFAOYSA-N 3,3-dimethylbutan-1-amine Chemical compound CC(C)(C)CCN GPWHFPWZAPOYNO-UHFFFAOYSA-N 0.000 description 1
- FPSPPRZKBUVEJQ-UHFFFAOYSA-N 4,6-dimethoxypyrimidine Chemical compound COC1=CC(OC)=NC=N1 FPSPPRZKBUVEJQ-UHFFFAOYSA-N 0.000 description 1
- XJFIKRXIJXAJGH-UHFFFAOYSA-N 5-chloro-1,3-dihydroimidazo[4,5-b]pyridin-2-one Chemical group ClC1=CC=C2NC(=O)NC2=N1 XJFIKRXIJXAJGH-UHFFFAOYSA-N 0.000 description 1
- DFGKGUXTPFWHIX-UHFFFAOYSA-N 6-[2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]acetyl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)C1=CC2=C(NC(O2)=O)C=C1 DFGKGUXTPFWHIX-UHFFFAOYSA-N 0.000 description 1
- DEXFNLNNUZKHNO-UHFFFAOYSA-N 6-[3-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperidin-1-yl]-3-oxopropyl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1CCN(CC1)C(CCC1=CC2=C(NC(O2)=O)C=C1)=O DEXFNLNNUZKHNO-UHFFFAOYSA-N 0.000 description 1
- 240000004178 Anthoxanthum odoratum Species 0.000 description 1
- JDWQITFHZOBBFE-UHFFFAOYSA-N Benzofenap Chemical compound C=1C=C(Cl)C(C)=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OCC(=O)C1=CC=C(C)C=C1 JDWQITFHZOBBFE-UHFFFAOYSA-N 0.000 description 1
- 239000005484 Bifenox Substances 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- BMZGGRRZOFWTCI-UHFFFAOYSA-N C(S(=O)(=S)O)(Cl)Cl Chemical group C(S(=O)(=S)O)(Cl)Cl BMZGGRRZOFWTCI-UHFFFAOYSA-N 0.000 description 1
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- 239000000725 suspension Substances 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 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 description 1
- RBTVSNLYYIMMKS-UHFFFAOYSA-N tert-butyl 3-aminoazetidine-1-carboxylate;hydrochloride Chemical compound Cl.CC(C)(C)OC(=O)N1CC(N)C1 RBTVSNLYYIMMKS-UHFFFAOYSA-N 0.000 description 1
- AHTPATJNIAFOLR-UHFFFAOYSA-N thifensulfuron-methyl Chemical group S1C=CC(S(=O)(=O)NC(=O)NC=2N=C(OC)N=C(C)N=2)=C1C(=O)OC AHTPATJNIAFOLR-UHFFFAOYSA-N 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- DNVLJEWNNDHELH-UHFFFAOYSA-N thiocyclam Chemical compound CN(C)C1CSSSC1 DNVLJEWNNDHELH-UHFFFAOYSA-N 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
- 229940098465 tincture Drugs 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- 238000009736 wetting Methods 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
- A01N25/12—Powders or granules
- A01N25/14—Powders or granules wettable
-
- 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
- A01N25/30—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 characterised by the surfactants
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2002097125 | 2002-03-29 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW200306153A true TW200306153A (en) | 2003-11-16 |
| TWI306736B TWI306736B (enExample) | 2009-03-01 |
Family
ID=28671857
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW092106985A TW200306153A (en) | 2002-03-29 | 2003-03-27 | Granular agricultural-chemical composition |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US20050250648A1 (enExample) |
| EP (1) | EP1498030B1 (enExample) |
| JP (1) | JP4603797B2 (enExample) |
| KR (1) | KR100987591B1 (enExample) |
| CN (1) | CN1307873C (enExample) |
| AT (1) | ATE546043T1 (enExample) |
| AU (1) | AU2003221025A1 (enExample) |
| BR (1) | BRPI0308777B1 (enExample) |
| CO (1) | CO5611059A2 (enExample) |
| TW (1) | TW200306153A (enExample) |
| WO (1) | WO2003082008A1 (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100581359C (zh) * | 2003-09-26 | 2010-01-20 | 组合化学工业株式会社 | 粒状农药制剂 |
| WO2005029956A1 (ja) * | 2003-09-26 | 2005-04-07 | Kumiai Chemical Industry Co., Ltd. | 均一拡散性粒状農薬製剤 |
| WO2006016527A1 (ja) * | 2004-08-11 | 2006-02-16 | Kumiai Chemical Industry Co., Ltd. | 農薬組成物 |
| JP5128087B2 (ja) * | 2005-06-23 | 2013-01-23 | バイエルクロップサイエンス株式会社 | 混合粒状農薬組成物 |
| WO2007007629A1 (ja) * | 2005-07-08 | 2007-01-18 | Kumiai Chemical Industry Co., Ltd. | 除草剤組成物 |
| US20110178299A1 (en) * | 2008-10-17 | 2011-07-21 | Kumiai Chemical Industry Co., Ltd. | Optically active difluoromethanesulfonanilide derivative and herbicide |
| CH705167A1 (fr) | 2011-06-16 | 2012-12-31 | Haute Ecole D Ingenierie Et De Gestion Du Canton De Vaud Heig Vd | Procédé et dispositif de mesure de la pression intraoculaire. |
| MX2019013379A (es) * | 2017-05-10 | 2020-08-03 | Thankappan Vadakekuttu | Composiciones agricolas. |
| SI3658166T1 (sl) * | 2017-07-27 | 2024-07-31 | SAWANT, Arun Vitthal | Sestava rastlinskega hranila |
| JP7184444B2 (ja) * | 2018-09-20 | 2022-12-06 | エルジー・ケム・リミテッド | 溶出制御型農薬粒剤及びその製造方法 |
Family Cites Families (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB512739A (en) | 1937-09-03 | 1939-09-25 | Cincinnati Milling Machine Co | Improvements in or relating to milling machines |
| JPS5634606A (en) | 1979-08-29 | 1981-04-06 | Sumitomo Chem Co Ltd | Herbicidal composition with high stability |
| US4657581A (en) * | 1984-05-18 | 1987-04-14 | Sanyo Chemical Industries, Ltd. | Herbicidal amide compounds and their uses |
| JPS62161702A (ja) | 1986-01-09 | 1987-07-17 | Hokko Chem Ind Co Ltd | 薬害の軽減された水稲用除草剤 |
| JP2508012B2 (ja) | 1986-04-09 | 1996-06-19 | 日産化学工業株式会社 | 水田除草用粒剤 |
| JPH0618761B2 (ja) * | 1986-07-14 | 1994-03-16 | 花王株式会社 | 粒状農薬の製造方法 |
| JPS6335504A (ja) | 1986-07-31 | 1988-02-16 | Nissan Chem Ind Ltd | 放出制御させた除草用粒剤 |
| JPH0198106A (ja) * | 1987-10-09 | 1989-04-17 | Alps Electric Co Ltd | 磁気ヘッドおよびその製造方法 |
| JP2692213B2 (ja) | 1987-12-26 | 1997-12-17 | 日産化学工業株式会社 | 放出制御された水田除草用粒剤 |
| JPH01211504A (ja) * | 1988-02-19 | 1989-08-24 | Kumiai Chem Ind Co Ltd | 固状農薬組成物 |
| US5441923A (en) * | 1988-09-02 | 1995-08-15 | E. I. Du Pont De Nemours And Company | Water-soluble or water dispersible pesticide granules comprising sulfonylurea herbicides in a polyethylene or polypropylene coating |
| GB8823288D0 (en) * | 1988-10-04 | 1988-11-09 | Schering Agrochemicals Ltd | Herbicides |
| JPH0372407A (ja) | 1989-05-30 | 1991-03-27 | Takeda Chem Ind Ltd | 除草剤組成物 |
| JP2969475B2 (ja) * | 1990-11-29 | 1999-11-02 | 北興化学工業株式会社 | 安定な水和顆粒状農薬 |
| EP0496701B1 (de) | 1991-01-25 | 1996-03-06 | Ciba-Geigy Ag | Sulfonylharnstoffe als Herbizide |
| 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 |
| GB9109599D0 (en) * | 1991-05-03 | 1991-06-26 | Dow Chemical Co | Herbicidal compositions with reduced phytotoxicity |
| DE59207084D1 (de) * | 1991-05-18 | 1996-10-17 | Hoechst Schering Agrevo Gmbh | Wässrige Dispersionen von Sulfonylharnstoffderivaten |
| WO1993000011A1 (en) * | 1991-06-21 | 1993-01-07 | E.I. Du Pont De Nemours And Company | Herbicidal composition for paddy fields |
| MY111437A (en) * | 1992-07-31 | 2000-05-31 | Monsanto Co | Improved glyphosate herbicide formulation. |
| JPH07215804A (ja) * | 1994-02-04 | 1995-08-15 | Harada Service:Kk | 農薬等放出制御材 |
| JP3660380B2 (ja) * | 1994-12-19 | 2005-06-15 | 住化武田農薬株式会社 | 農薬粒剤 |
| JPH08283108A (ja) | 1995-04-12 | 1996-10-29 | Nissan Chem Ind Ltd | 除草用固型製剤 |
| JP3270819B2 (ja) * | 1997-02-13 | 2002-04-02 | 北興化学工業株式会社 | 湛水下水田の直接散布用水性懸濁製剤 |
| JP3618510B2 (ja) * | 1997-03-14 | 2005-02-09 | 北興化学工業株式会社 | 湛水下水田の直接散布用水性懸濁製剤 |
| JPH11269015A (ja) * | 1998-03-18 | 1999-10-05 | Nissan Chem Ind Ltd | 除草剤組成物 |
| JP4216363B2 (ja) * | 1998-03-18 | 2009-01-28 | クミアイ化学工業株式会社 | 成分が安定化された固体農薬組成物 |
| WO2000006553A1 (en) * | 1998-07-29 | 2000-02-10 | Ihara Chemical Industry Co., Ltd. | Di- or tri-fluoromethanesulfonyl anilide derivatives, process for the preparation of them and herbicides containing them as the active ingredient |
| JP3632947B2 (ja) * | 1998-07-29 | 2005-03-30 | クミアイ化学工業株式会社 | ジフルオロメタンスルホニルアニリド誘導体、その製造方法及びそれを有効成分とする除草剤 |
| JP4347446B2 (ja) * | 1999-02-26 | 2009-10-21 | 日本エンバイロケミカルズ株式会社 | マイクロカプセル化シロアリ防除剤およびその製造方法 |
| JP3607652B2 (ja) * | 2000-09-14 | 2005-01-05 | 花王株式会社 | 殺菌剤組成物 |
-
2003
- 2003-03-24 AT AT03712864T patent/ATE546043T1/de active
- 2003-03-24 JP JP2003579562A patent/JP4603797B2/ja not_active Expired - Lifetime
- 2003-03-24 EP EP03712864A patent/EP1498030B1/en not_active Expired - Lifetime
- 2003-03-24 US US10/508,162 patent/US20050250648A1/en not_active Abandoned
- 2003-03-24 WO PCT/JP2003/003542 patent/WO2003082008A1/ja not_active Ceased
- 2003-03-24 CN CNB038069075A patent/CN1307873C/zh not_active Expired - Fee Related
- 2003-03-24 BR BRPI0308777A patent/BRPI0308777B1/pt not_active IP Right Cessation
- 2003-03-24 AU AU2003221025A patent/AU2003221025A1/en not_active Abandoned
- 2003-03-24 KR KR1020047014878A patent/KR100987591B1/ko not_active Expired - Lifetime
- 2003-03-27 TW TW092106985A patent/TW200306153A/zh not_active IP Right Cessation
-
2004
- 2004-10-04 CO CO04098565A patent/CO5611059A2/es active IP Right Grant
-
2006
- 2006-12-27 US US11/645,615 patent/US7638506B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| CN1307873C (zh) | 2007-04-04 |
| KR100987591B1 (ko) | 2010-10-12 |
| TWI306736B (enExample) | 2009-03-01 |
| US20050250648A1 (en) | 2005-11-10 |
| EP1498030A4 (en) | 2010-12-22 |
| BR0308777A (pt) | 2004-12-28 |
| US7638506B2 (en) | 2009-12-29 |
| EP1498030B1 (en) | 2012-02-22 |
| US20070105720A1 (en) | 2007-05-10 |
| JP4603797B2 (ja) | 2010-12-22 |
| JPWO2003082008A1 (ja) | 2005-07-28 |
| CO5611059A2 (es) | 2006-02-28 |
| EP1498030A1 (en) | 2005-01-19 |
| ATE546043T1 (de) | 2012-03-15 |
| WO2003082008A1 (en) | 2003-10-09 |
| AU2003221025A1 (en) | 2003-10-13 |
| BRPI0308777B1 (pt) | 2015-10-13 |
| KR20040099351A (ko) | 2004-11-26 |
| CN1642416A (zh) | 2005-07-20 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | Annulment or lapse of patent due to non-payment of fees |