CN1022284C - 除草组合物 - Google Patents
除草组合物 Download PDFInfo
- Publication number
- CN1022284C CN1022284C CN88104874A CN88104874A CN1022284C CN 1022284 C CN1022284 C CN 1022284C CN 88104874 A CN88104874 A CN 88104874A CN 88104874 A CN88104874 A CN 88104874A CN 1022284 C CN1022284 C CN 1022284C
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- Expired - Lifetime
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- 239000000203 mixture Substances 0.000 title claims abstract description 25
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 24
- 150000001875 compounds Chemical class 0.000 claims abstract description 65
- -1 pyridine sulfamide compound Chemical class 0.000 claims description 32
- QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical compound COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 claims description 8
- 229940095102 methyl benzoate Drugs 0.000 claims description 4
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 3
- FYYXUCQRIUAYEH-UHFFFAOYSA-N CNC.C(C)OCC(=O)O.ClC1=CC=CC(=C1)Cl Chemical compound CNC.C(C)OCC(=O)O.ClC1=CC=CC(=C1)Cl FYYXUCQRIUAYEH-UHFFFAOYSA-N 0.000 claims 1
- 150000003839 salts Chemical class 0.000 abstract description 11
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract description 7
- DWJMBQYORXLGAE-UHFFFAOYSA-N pyridine-2-sulfonamide Chemical class NS(=O)(=O)C1=CC=CC=N1 DWJMBQYORXLGAE-UHFFFAOYSA-N 0.000 abstract description 4
- MZZBPDKVEFVLFF-UHFFFAOYSA-N cyanazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C#N)=N1 MZZBPDKVEFVLFF-UHFFFAOYSA-N 0.000 abstract description 3
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 abstract description 2
- WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 abstract description 2
- 239000005591 Pendimethalin Substances 0.000 abstract description 2
- IBZHOAONZVJLOB-UHFFFAOYSA-N Tridiphane Chemical compound ClC1=CC(Cl)=CC(C2(CC(Cl)(Cl)Cl)OC2)=C1 IBZHOAONZVJLOB-UHFFFAOYSA-N 0.000 abstract 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 abstract description 2
- MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 abstract description 2
- 125000005843 halogen group Chemical group 0.000 abstract 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 abstract 1
- VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 abstract 1
- 239000005476 Bentazone Substances 0.000 abstract 1
- 239000005489 Bromoxynil Substances 0.000 abstract 1
- 239000005504 Dicamba Substances 0.000 abstract 1
- XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 abstract 1
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 abstract 1
- ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical compound C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 abstract 1
- CNBGNNVCVSKAQZ-UHFFFAOYSA-N benzidamine Natural products C12=CC=CC=C2C(OCCCN(C)C)=NN1CC1=CC=CC=C1 CNBGNNVCVSKAQZ-UHFFFAOYSA-N 0.000 abstract 1
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 abstract 1
- 238000009472 formulation Methods 0.000 description 17
- 239000004009 herbicide Substances 0.000 description 17
- 239000000843 powder Substances 0.000 description 14
- 244000025254 Cannabis sativa Species 0.000 description 12
- 235000010086 Setaria viridis var. viridis Nutrition 0.000 description 12
- 244000304962 green bristle grass Species 0.000 description 12
- 238000009736 wetting Methods 0.000 description 10
- 241000196324 Embryophyta Species 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 240000008042 Zea mays Species 0.000 description 7
- 239000002585 base Substances 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- 240000006122 Chenopodium album Species 0.000 description 6
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 6
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 6
- 125000004429 atom Chemical group 0.000 description 6
- 235000009973 maize Nutrition 0.000 description 6
- 238000005507 spraying Methods 0.000 description 6
- FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 5
- 240000006995 Abutilon theophrasti Species 0.000 description 5
- 244000201986 Cassia tora Species 0.000 description 5
- 235000014552 Cassia tora Nutrition 0.000 description 5
- FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000002689 soil Substances 0.000 description 5
- UENGBOCGGKLVJJ-UHFFFAOYSA-N 2-chloro-1-(2,4-difluorophenyl)ethanone Chemical compound FC1=CC=C(C(=O)CCl)C(F)=C1 UENGBOCGGKLVJJ-UHFFFAOYSA-N 0.000 description 4
- 239000005995 Aluminium silicate Substances 0.000 description 4
- 235000006719 Cassia obtusifolia Nutrition 0.000 description 4
- 235000009344 Chenopodium album Nutrition 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- 235000003403 Limnocharis flava Nutrition 0.000 description 4
- 235000012211 aluminium silicate Nutrition 0.000 description 4
- 235000013339 cereals Nutrition 0.000 description 4
- 125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 235000011498 Chenopodium album var missouriense Nutrition 0.000 description 3
- 235000013328 Chenopodium album var. album Nutrition 0.000 description 3
- 235000014052 Chenopodium album var. microphyllum Nutrition 0.000 description 3
- 235000014050 Chenopodium album var. stevensii Nutrition 0.000 description 3
- 235000013012 Chenopodium album var. striatum Nutrition 0.000 description 3
- 244000058871 Echinochloa crus-galli Species 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- 240000006410 Sida spinosa Species 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 244000067505 Xanthium strumarium Species 0.000 description 3
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- WJJBIYLGJUVNJX-UHFFFAOYSA-N pyrimidine-2-sulfonamide Chemical compound NS(=O)(=O)C1=NC=CC=N1 WJJBIYLGJUVNJX-UHFFFAOYSA-N 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 229920005552 sodium lignosulfonate Polymers 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 244000152970 Digitaria sanguinalis Species 0.000 description 2
- 235000010823 Digitaria sanguinalis Nutrition 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- 240000001549 Ipomoea eriocarpa Species 0.000 description 2
- 235000005146 Ipomoea eriocarpa Nutrition 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 235000005687 corn oil Nutrition 0.000 description 2
- 239000002285 corn oil Substances 0.000 description 2
- 230000001186 cumulative effect Effects 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 229940043265 methyl isobutyl ketone Drugs 0.000 description 2
- YZHUMGUJCQRKBT-UHFFFAOYSA-M sodium chlorate Chemical compound [Na+].[O-]Cl(=O)=O YZHUMGUJCQRKBT-UHFFFAOYSA-M 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000000375 suspending agent Substances 0.000 description 2
- 239000004408 titanium dioxide Substances 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- ZMANZCXQSJIPKH-UHFFFAOYSA-N triethylamine Natural products CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 2
- MZXGZMPPXQETLI-UHFFFAOYSA-N (2-methylanilino) acetate Chemical class CC(=O)ONC1=CC=CC=C1C MZXGZMPPXQETLI-UHFFFAOYSA-N 0.000 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- VIETUFSZPCIVQL-UHFFFAOYSA-N 1-methyl-3h-pyrrol-2-one Chemical class CN1C=CCC1=O VIETUFSZPCIVQL-UHFFFAOYSA-N 0.000 description 1
- CGPTZCZFFUYDCB-UHFFFAOYSA-N 2-bromo-4-hydroxybenzonitrile Chemical compound OC1=CC=C(C#N)C(Br)=C1 CGPTZCZFFUYDCB-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 244000237956 Amaranthus retroflexus Species 0.000 description 1
- 235000013479 Amaranthus retroflexus Nutrition 0.000 description 1
- XIDISDMXAZGTQC-UHFFFAOYSA-N C(C)OC(COCC)=O.ClC1=CC=CC(=C1)Cl Chemical compound C(C)OC(COCC)=O.ClC1=CC=CC(=C1)Cl XIDISDMXAZGTQC-UHFFFAOYSA-N 0.000 description 1
- QOFJYAIAWNGTOH-UHFFFAOYSA-N C(C)OCC(=O)O.ClC1=CC=CC(=C1)Cl Chemical compound C(C)OCC(=O)O.ClC1=CC=CC(=C1)Cl QOFJYAIAWNGTOH-UHFFFAOYSA-N 0.000 description 1
- FLIQZZAJPCIEKH-UHFFFAOYSA-N COC1=CC(=C(C=C1)C(=O)O)OCl Chemical compound COC1=CC(=C(C=C1)C(=O)O)OCl FLIQZZAJPCIEKH-UHFFFAOYSA-N 0.000 description 1
- 240000006432 Carica papaya Species 0.000 description 1
- 244000146553 Ceiba pentandra Species 0.000 description 1
- 235000003301 Ceiba pentandra Nutrition 0.000 description 1
- 240000003176 Digitaria ciliaris Species 0.000 description 1
- 235000017898 Digitaria ciliaris Nutrition 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical class 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 1
- 241000207890 Ipomoea purpurea Species 0.000 description 1
- 240000000249 Morus alba Species 0.000 description 1
- 235000008708 Morus alba Nutrition 0.000 description 1
- 235000011999 Panicum crusgalli Nutrition 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 235000019774 Rice Bran oil Nutrition 0.000 description 1
- 235000007244 Zea mays Nutrition 0.000 description 1
- JEUOICSEUHSRJV-UHFFFAOYSA-N [NH4+].N=NC=NN.N=NC=NN.C(C)OCC(=O)[O-].ClC1=CC=CC(=C1)Cl Chemical compound [NH4+].N=NC=NN.N=NC=NN.C(C)OCC(=O)[O-].ClC1=CC=CC(=C1)Cl JEUOICSEUHSRJV-UHFFFAOYSA-N 0.000 description 1
- NDXWUNHOHWBFCP-UHFFFAOYSA-N [Na].C(C)OCC(=O)O.ClC1=CC=CC(=C1)Cl Chemical compound [Na].C(C)OCC(=O)O.ClC1=CC=CC(=C1)Cl NDXWUNHOHWBFCP-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 229940077388 benzenesulfonate Drugs 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 239000010495 camellia oil Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- YOMFVLRTMZWACQ-UHFFFAOYSA-N ethyltrimethylammonium Chemical compound CC[N+](C)(C)C YOMFVLRTMZWACQ-UHFFFAOYSA-N 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000002420 orchard Substances 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 229920000259 polyoxyethylene lauryl ether Polymers 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 239000008165 rice bran oil Substances 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
- 150000004992 toluidines Chemical class 0.000 description 1
- 239000002383 tung oil Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000009333 weeding 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
- A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
- A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
- A01N41/04—Sulfonic acids; Derivatives thereof
- A01N41/06—Sulfonic acid amides
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
-
- 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
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Abstract
本发明为式(I)的吡啶磺酰胺除草化合物及其盐与至少一种选自包括2,4-二氯苯氧基乙酸二甲铵、2-[[[4,6-双-(二氟甲氧基)-嘧啶-2-基]氨羰基]氨磺酰基]苯甲酸甲酯以及3,5-二溴-4-羟苄腈的一种除草化合物的混合物。
Description
本发明涉及除草组合物,其中含有作为有效组分的至少一种选自吡啶磺酰胺类及其盐的化合物和至少一种特定的其它除草化合物。
在日本专利申请No62-8286(日本专利公开No62-178588,1987.8.5)中公开了如下式之吡啶磺酰胺化合物及其盐类:
(式中R1和R2为氢原子或烷基;X和Y为甲基或甲氧基;A为=CH-基或=N-基)。此专利申请还公开了将上述之吡啶磺酰胺化合物与另一除草化合物混合,可混合的除草剂有3,6-二氯二甲氧基苯甲酸、3-(1-甲基乙基)-1H-2,1,3-苯并噻二嗪-4(3H)-酮-2,2-二氧化物、2-(4-氯-6-乙氨基-1,3,5-三嗪-2-基氨基)-2-甲基丙腈、2-氯-4-乙基氨基-6-异丙基氨基-1,3,5-三嗪、2,4-二氯苯氧基乙酸乙酯、2-(3,5-二氯苯基)-2-(2,2,2-三氯乙基)环氧乙烷、N-(1-乙丙基)-2,6-二硝基-3,4-二甲代苯胺、2-氯-2′,6′-二乙基-N-(甲氧基甲基)乙酰苯胺、2-氯-6′-乙基-N-(2-甲氧基-1-甲基乙基)乙酰基-O-甲苯胺及类似物,但没有给出特定的生物试验数据。
欧洲专利申请No87300502.9(公开号232,067,1987,8,12.)和No87301954.1(公开号237,292,1987,9,16)也部分公开将上述的吡啶磺酰胺化合物与如日本专利申请No62-8286所述的另一除草化合物混合,也未给出特定的生物试验数据。
本发明提供一类除草组合物,此组合物包括至少一种选自式(Ⅰ)的吡啶磺酰胺化合物和其盐类的化合物作为有效组分
(式中的X为氢原子、囟原子或可被1-3个囟原子取代的甲基;R为氢原子或甲基)和至少一种选自包括下述一组化合物的化合物:2,4-二氯苯氧基乙酸和其烷基酯及其盐、3,6-二氯-2-甲氧基苯甲酸、2-氯-4-乙胺基-6-异丙胺基-1,3,5-三嗪、3-(1-甲基乙基)-1H-2,1,3-苯并噻二嗪-4(3H)-酮-2,2-二氧化物、2-氯-2′,6′-二乙基-N-(甲氧基甲基)乙酰苯胺、2-氯-6′-乙基-N-(2-甲氧基-1-甲基乙基)乙酰-O-甲苯胺、2-氯-N-异丙基乙酰苯胺、N-(1-乙基丙基)-2,6-二硝基-3,4-二甲代苯胺、2-(3,5-二氯苯基)-2-(2,2,2-三氯乙基)环氧乙烷、2-氯-4-(1-氰基-1-甲基乙胺基)-6-乙胺基-1,3,5-三嗪、2-[[[4,6-双(二氟甲氧基)-吡啶-2-基]氨基羰基]氨基磺酰基]苯甲酸甲酯及其盐、3,5-二溴-4-羟基苄腈、5,7-二甲基-N-(2,6-二氯苯基)-1,2,4-三唑基[1,5-a]嘧啶-2-磺酰胺和2-氯-N-(乙氧基甲基)-2′-乙基-6′-甲基乙酰苯胺。
本发明的除草组合物比任何单独使用的化合物有更广的除莠谱,并在整个谷类生长期只需一次喷洒就可有充份的除莠效果。
通常,各种莠草是生存在一起的,但是它们的萌芽和生长期又因莠草的不同而不同,在喷洒除草剂时不可避免地要喷洒于各种莠草的不同生长期。事实上,只经一次喷洒除莠剂要杀灭各种莠草是相当困难的。假如一些莠草存活下来了,随后其中一些会生长出来,另一些会再萌芽,即使它
们的地上部分已被杀灭。其结果是,它们最终仍会浓密生长。因此,此时喷洒除草剂的效果会减半。所以,研究一种除草广谱、对生长完全的莠草有效并能对莠草有足够时间的控制作用的除草剂仍然是十分需要的。
申请人曾递交过一专利申请(日本专利申请No62-17323),是基于上述由式(Ⅰ)代表的化合物及其盐对于许多种莠草(包括那些极其有害的莠草)有很高的除草效果而对谷类无害这一发现的。这些化合物虽然依赖于包括使用量和使用时间等的条件,但常常不能完全消灭某些特殊种类的莠草;并且在施用任何一种上述化合物后常常有新的莠草从施药区的土壤中生长出来。
从解决上述问题出发,本发明的发明人,将式(Ⅰ)的吡啶磺酰胺化合物与各种不同的除草化合物结合使用,结果发现,使用选自式(Ⅰ)的吡啶化合物和其盐的至少一种化合物与至少一种其它特定的除草化合物(下面即将述及)的混合物比使用单一的化合物有更广的除莠谱,并且只喷洒一次这样的混合物就可在谷类整个生长时期保持足够的除莠效果。本发明是基于以上这些发现而完成的。
再者,按照本发明所提供的除草组合物,其特征在于它包括至少一种选自以式(Ⅰ)代表的吡啶磺酰胺化合物及其盐类作为有效组分
(式中X为氢原子、囟原子或可被1-3个囟原子取代的甲基;R为氢原子或甲基)和至少一种选自下面一组化合物的化合物:2,4-二氯苯氧基乙酸及其烷基酯和其盐、3,6-二氯-2-甲氧基苯甲酸、2-氯-4-乙胺基-6-异丙胺基-1,3,5-三嗪、3-(1-甲基乙基)-1H-2,1,3-苯并噻二嗪-4-(3
H)-酮-2,2-二氧化合物、2-氯-2′,6′-二乙基-N-(甲氧基甲基)乙酰苯胺、2-氯-6′-乙基-N-(2-甲氧基-1-甲基乙基)乙酰基-O-甲苯胺、2-氯-N-异丙基乙酰苯胺、N-(1-乙基丙基)-2,6-二硝基-3,4-二甲代苯胺、2-(3,5-二氯苯基)-2-(2,2,2-三氯乙基)环氧乙烷、2-氯-4-(1-氰基-1-甲基乙胺基)-6-乙胺基-1,3,5-三嗪、2-[[[4,6-双(二氟甲氧基)-嘧啶-α-基]氨基羰基]氨基磺酰基]苯甲酸甲酯和其盐、3,5-二溴-4-羟基苄腈、5,7-二甲基-N-(2,6-二氯苯基)-1,2,4-三唑基[1,5-a]嘧啶-2-磺酰胺、2-氯-N-(乙氧基甲基)-2′-乙基-6′-甲基乙酰苯胺。
作为式(Ⅰ)中X的囟原子或式(Ⅰ)中X为甲基时的取代囟原子的,有氟原子、氯原子、溴原子和碘原子。
本发明除草化合物的盐类有碱金属盐(如钠盐或钾盐)、碱土金属盐(如镁盐或钙盐)、胺盐(如单乙胺、二乙胺或三乙胺盐)或季铵碱(如三甲基乙基铵阳离子或四甲基铵阳离子)。
以式(Ⅰ)代表的吡啶磺酰胺化合物及其盐类包括下面表1中的化合物:
与式(Ⅰ)表代的吡啶磺酰胺化合物混合使用的特定除草化合物包括那些悉知有商品名或普通名称的化合物,如表2所述。
表1
化合物号 X R 熔点(℃)
A-1 H CH3169-173
A-2 H H 147-149.5
A-3 Cl CH3183-186
A-4 Br CH3201.5-203.5
A-5 CH3CH3170-174
A-6 CHF2CH3194-195
A-7 化合物№A-1钠盐 195-215
(分解)
A-8 化合物№A-2单乙胺盐 125-128
表2
化合物号 化合物 商品名或普通名
B-1 2,4-二氯苯氧基乙酸 2,4-D
B-2 2,4-二氯苯氧基乙酸钠 ″
B-3 2,4-二氯苯氧基乙酸二甲铵盐 ″
B-4 2,4-二氯苯氧基乙酸乙酯 ″
B-5 3,6-二氯-2-甲氧基苯甲酸 麦草畏
B-6 2-氯-4-乙胺基-6-异丙胺基 阿特粒津
-1,3,5-三嗪
B-7 3-(1-甲基乙基)1H-2,1,3- 噻草平
苯并噻二嗪-4(3H)-酮-
2,2-二氧化合物
B-8 2-氯-2′,6′-二乙基-N- 草不缘
(甲氧基甲基)乙酰苯胺
B-9 2-氯-6′-乙基-N-(2-甲 甲氧毒草安
氧基-1-甲基乙基)乙酰基-O-
甲苯胺
B-10 2-氯-N-异丙基乙酰苯胺 毒草安
N-(1-乙基丙基)-2,6-二硝基
-3,4-二甲代苯胺
B-11 2-(3,5-二氯苯基)-2-(2, Pendimethalin
B-12 2,2-三氯乙基)环氧乙烷 Tridiphane
表2(续)
化合物号 化合物 商品名或普通名
B-13 2-氯-4-(1-氰基-1-甲基 草净津
乙胺基)-6-乙胺基-1,3,5-
三嗪
B-14 2-〔〔〔4,6-双(二氟甲氧基) -
-嘧啶-2-基〕氨基羰基〕氨基
磺酰基〕苯甲酸甲酯
B-15 化合物№B-14钠盐 -
B-16 3,5-二溴-4-羟基苯甲腈 溴苯腈
B-17 5,7-二甲基-N-(2,6-二 -
氯苯基)-1,2,4-三唑基
〔1,5-a〕嘧啶-2-磺酰胺
B-18 2-氯-N-(乙氧甲基)-2′- 乙基乙草安
乙基-6′-甲基乙腈
以式(Ⅰ)代表的吡啶磺酰胺及其盐与特定的除草化合物的重量比一般在1∶800至200∶1,理想的是1∶200至20∶1。化合物的恰当施用量不能单独而定,因其根据制剂的形式、施用的时间和莠草的种类等因素而有不同。但是,一般说来,以式(Ⅰ)代表的吡啶磺酰胺化合物或其盐的用量约为0.05~10g/a,特定的其它除草化合物的用量约为0.05~40g/a。
本发明的化合物可施于包括高地田、果园、桑田、森林、农业道路、庭园、工厂等各种地区。除草组合物的施用方法可以任意选择土壤处理或叶片处理。
本发明的除草组合物的制备是按任何制备农业制剂惯用的方法将各种辅助剂与式(Ⅰ)代表的吡啶磺酰胺和特定的其它除草化合物混合,制成可乳化浓缩物、可湿性粉剂、悬浮剂浓缩物、粒剂、粉剂、水溶性粉剂或其它剂型。式(Ⅰ)代表的吡啶磺酰胺化合物和特定的其它除草化合物可以混合在一起制成制剂,或者分别制成制剂后,再将它们混合在一起。上述的辅助剂包括固体载体(如硅藻土、消石灰、碳酸钙、滑石、白炭、高岭土、膨润土、Jeaklite、水溶性沉淀粉、碳酸氢钠);溶剂(甲苯、二甲苯、溶剂石脑油、乙醇、二氧杂环己烷、丙酮、异佛尔酮、甲基异丁基酮、二甲基甲酰胺、N-甲基-2-吡咯酮);铺展剂和表面活性剂(如烷基硫酸钠、烷基苯磺酸钠、木素磺酸钠、聚氧乙二醇烷基醚、聚氧乙烯月桂基醚、聚氧乙烯烷芳基醚、聚氧乙烯脂肪酸酯、聚氧乙烯脱水山梨醇脂肪酸酯);植物油和矿物油(如橄榄油、爪哇木棉油、蓖麻油、番木瓜油、山茶油、可可油、芝麻油、玉米油、米糠油、花生油、棉籽油、豆油、菜籽油、亚麻子油、桐油、液体石蜡)。
下面是本发明除草组合物的实施例叙述,但本发明并不局限于此。
配方实施例1:
(1)化合物NoA-1 1份(重量)
(2)化合物NoB-1至B-18 各2.5份(重量)
(3)Dikssol W-92 2份(重量)
(4)Newlite 94.5份(重量)
将上列各组分混合并磨碎,得到粉剂。
配方实施例2:
(1)化合物NoA-1 5份(重量)
(2)化合物NoB-1至B-18 各37.5份(重量)
(3)Dikssol W-66 5份(重量)
(4)Dikssol W-0913 2份(重量)
(5)硅藻土 50.5份(重量)
将上列各组分混合制成可湿性粉剂。
配方实施例3:
(1)化合物NoA-1 5份(重量)
(2)化合物NoB-1至B-18 各50份(重量)
(3)Sorpol 5050 3份(重量)
(4)Sorpol 5073 4份(重量)
(5)Hi-Filler No10 38份(重量)
将上列各组分混合,制成可湿性粉剂。
配方实施例4:
(1)化合物NoA-1 1份(重量)
(2)化合物NoB-1至B-18 各15份(重量)
(3)Sorpol 5039 5份(重量)
(4)Lavelin S 2份(重量)
(5)Carplex #80 15份(重量)
(6)高岭土 62份(重量)
将上列各组分混合,制成可湿性粉剂。
配方实施例5:
(1)化合物NoA-1 0.1份(重量)
(2)化合物NoB-1至B-18 各1份(重量)
(3)Didssol W-92 2份(重量)
(4)Newlite 96.9份(重量)
将上列各组分混合并磨碎,制成粉剂。
配方实施例6:
(1)化合物NoA-1 1份(重量)
(2)化合物NoB-1至B-18 各20份(重量)
(3)Dikssol W-66 5份(重量)
(4)Dikssol W-0913 2份(重量)
(5)硅藻土 72份(重量)
将上述各组分混合,制成可湿性粉剂。
配方实施例7:
(1)化合物NoA-1 20份(重量)
(2)化合物NoB-1至B-18 各40份(重量)
(3)Sorpol 5039 5份(重量)
(4)Lavelin S 2份(重量)
(5)高岭土 33份(重量)
将上述各组分混合,制成可湿性粉剂。
配方实施例8:
(1)化合物NoA-1 4份(重量)
(2)化合物NoB-1至B-18 各30份(重量)
(3)Didssol W-66 5份(重量)
(4)Didssol W-9013 2份(重量)
(5)硅藻土 59份(重量)
将上述各组分混合,制成可湿性粉剂。
配方实施例9:
(1)化合物NoA-1 0.2份(重量)
(2)化合物NoB-1至B-18 各1份(重量)
(3)Didssol W-92 2份(重量)
(4)Newlite 96.8份(重量)
将上述各组分混合并磨碎,制成粉剂。
配方实施例10:
(1)化合物NoA-7 10份(重量)
(2)化合物NoB-2,B-3或B-15 50份(重量)
(3)木素磺酸钠 5份(重量)
(4)水溶性淀粉 35份(重量)
将上述各组分混合并磨碎,制成水溶性粉剂。
配方实施例11:
(1)化合物NoA-1 5份(重量)
(2)化合物NoB-1至B-18 各5份(重量)
(3)Didssol W-66 5份(重量)
(4)Didssol W-9013 2份(重量)
(5)硅藻土 83份(重量)
将上述各组分混合,制成可湿性粉剂。
配方实施例12:
(1)化合物NoA-5 15份(重量)
(2)化合物NoB-1至B-18 各10份(重量)
(3)Sorpol 5050 3份(重量)
(4)Sorpol 5073 4份(重量)
(5)Hi-Filler No10 68份(重量)
将上述各组分混合,制成可湿性粉剂。
配方实施例13:
(1)化合物NoA-1 40份(重量)
(2)化合物NoB-1至B-18 各10份(重量)
(3)Sorpol 5039 5份(重量)
(4)Lavelin S 2份(重量)
(5)Carplex #80 18份(重量)
(6)高岭土 28份(重量)
将上述各组分混合,制成可湿性粉剂。
配方实施例14:
(1)化合物NoA-1 5份(重量)
(2)化合物NoB-2,B-3或B-15 各5份(重量)
(3)木素磺酸钠 5份(重量)
(4)水溶性淀粉 85份(重量)
将上述各组分混合,制成水溶性粉剂。
配方实施例15:
(1)化合物NoA-1 3份(重量)
(2)化合物NoB-1至B-3 各2份(重量)
B-5至B-7,B-13至B-18
(3)玉米油 81份(重量)
(4)Sorpol 3815 12份(重量)
(5)膨润土-烷基胺复合物 2份(重量)
将上述各组分混合均匀,用Dyno-Mill(Willy A.Bachofen AG)研磨机研磨,制得悬浮剂浓缩物。
[注]
Dikssol W-92,W-66,W-0913,Lavelin S:
Dai-ichi Kogyo Seiyaku Co.,Ltd.产品的商品名
Newlite:Nippon Taikagenryo Co.,Ltd.产品商品名
Sorpol 5050,5073,5039,3815:
Toho Chemical Co.,Ltd.产品商品名
Hi-Filler No10:Matsumura Sangyo Co.,Ltd.产品商品名
Carplex #80:Shionogi Co.,Ltd.产品商品名
本发明的除草组合物的生物试验实施例以试验实施例叙述于下,但本发明并不受这些实施例所限制。
试验实施例1:
将高地土壤盛于1/3,000公亩(a)的花盆和1/10,000公亩(a)的花盆中。将玉蜀黍(Zea mays)(品种:Royal Dent 105 T)播种于1/3,000公亩的花盆中,将Velvetleaf(Abutilon theo phrasti)、Sicklepod(Cassia tora)、Common lambsquarters(Chenopodium album)large crabgrass(Digitaria adscendens)分别播种于1/10,000公亩的花盆中。
当试验植物生长到各给定的生长期(玉蜀黍:4.2叶期;Velvetleaf:1.5叶期;Sicklepod:子叶期;Common lambquarters:子叶期至4叶期;large crabgrass:3叶期)时,将预定量的除草组合物用一小喷洒
枪进行叶面喷洒。预定量除草组合物按配方实施例7之方法制备,并稀释于5升[每公亩(a)]的水中,制备水溶液,再向其中加入总体积0.2%的农用铺展剂。喷洒后用肉眼观察植物的生长进展30天,按10级划分评价控制生长的程度(1:相同于未处理花盆中的植物生长情况-10:完全控制生长),其结果示于表3。
试验实施例2:
将高地土壤盛于1/3,000公亩(a)和1/10,100公亩(a)的花盆中,分别将玉蜀黍(品种Royal Dent 105 T)播种于1/3,000公亩的花盆中,将Velvetleaf、Sicklepod和common lambsquarters播种于1/10,000公亩的花盆中。
当试验植物生长到给定的生长期(玉蜀黍:4.2叶期;velvetleaf:2.5叶期;sicklepod:1.2叶期;common lambsquarters:2-4叶期)时,将预定量的除草组合物用小喷洒枪进行叶面喷洒。预定量的除草组合物稀释于5升(每公亩)的水中,制成水溶液,其中加入总体积0.2%的农用铺展剂。喷洒后,用肉眼观察物的生长进展26天,按10级(1:相同于未处理花盆中的植物生长情况-10:完全控制生长)评价控制生长的程度。其结果示于表4。
表4(续)
试验实施例3:
将高地土壤盛于1/1,500公亩(a)的花盆中分别播种玉蜀黍(品种:Royal Dent 105 T)、cocklebur(Xanthium strumarium)、牵牛花(Ipomoea purpurea)、Prickly sida(Sida spinosa)、藜(Amaranthus retroflexus)、稗(Echinochloa crusgalli)播种于花盆中。
当试验植物生长到各给定的生长期(玉蜀黍:2.5叶期;cocklebur 1.5叶期;牵牛花2.5中期;prickly sida和藜1.0叶期;稗:1.5叶期)时,将预定量的除草组合物用小喷洒枪进行叶面喷洒,预定量的除草组合物稀释于5升[每公亩(a)]水中,制成水溶液,其中加入总量0.2%的农用铺展剂。喷洒后用肉眼观察植物生长进展14天,按10级(1:相同于未处理的花盆中的植物生长情况-10:完全控制生长)。结果示于表5。
Claims (1)
1、一种除草组合物,该组合物由式(Ⅰ)代表的吡啶磺酰胺化合物
(Ⅰ)
和选自包括2,4-二氯苯氧基乙酸二甲铵、2-[[[4,6-双-(二氟甲氧基)-嘧啶-2-基]氨羰基]氨磺酰基]苯甲酸甲酯以及3,5-二溴-4-羟苄腈的一种化合物组成,其混合比为1∶0.01至40。
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP199287/87 | 1987-08-10 | ||
| JP19928787 | 1987-08-10 | ||
| JP13604388 | 1988-06-02 | ||
| JP136043/88 | 1988-06-02 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1031174A CN1031174A (zh) | 1989-02-22 |
| CN1022284C true CN1022284C (zh) | 1993-10-06 |
Family
ID=26469726
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN88104874A Expired - Lifetime CN1022284C (zh) | 1987-08-10 | 1988-08-09 | 除草组合物 |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | USH670H (zh) |
| EP (2) | EP0526796A2 (zh) |
| JP (1) | JP2696139B2 (zh) |
| KR (1) | KR930002953B1 (zh) |
| CN (1) | CN1022284C (zh) |
| AU (1) | AU608637B2 (zh) |
| BG (2) | BG48092A3 (zh) |
| BR (1) | BR8803777A (zh) |
| DE (1) | DE3888426T2 (zh) |
| EG (1) | EG18676A (zh) |
| ES (1) | ES2052727T3 (zh) |
| HU (1) | HU205834B (zh) |
| LV (1) | LV10019B (zh) |
| MY (1) | MY103546A (zh) |
| NZ (1) | NZ225473A (zh) |
| TR (3) | TR28196A (zh) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| YU48354B (sh) * | 1987-11-27 | 1998-07-10 | Ciba-Geigy Ag. | Herbicidno sredstvo sa sinergističnim dejstvom i postupak za njegovu pripremu |
| US5190576A (en) * | 1989-06-13 | 1993-03-02 | Rhone-Poulenc Agrochimie | Herbicidal combination based on bromoxynil or one of its derivatives |
| FR2648014B1 (fr) * | 1989-06-13 | 1993-06-11 | Rhone Poulenc Agrochimie | Association herbicide a base de bromoxynil ou de l'un de ses derives a effet synergique |
| DE3933543A1 (de) * | 1989-10-07 | 1991-04-11 | Hoechst Ag | Synergistische herbizide mittel |
| US5116405A (en) * | 1989-11-06 | 1992-05-26 | Nissan Chemical Industries Ltd. | Pyridinesulfonamide derivatives and herbicides |
| JPH04120006A (ja) * | 1990-08-23 | 1992-04-21 | Du Pont Japan Ltd | 水田用除草剤組成物 |
| EP0512738B1 (en) * | 1991-05-03 | 1997-01-22 | Dowelanco | Herbicidal compositions with increased crop safety |
| RO117587B1 (ro) * | 1991-07-12 | 2002-05-30 | Hoechst Ag | Compozitie erbicida, procedeu de obtinere a acesteia si metoda pentru controlul plantelor nedorite |
| DK0554015T3 (da) * | 1992-01-28 | 1995-06-06 | Ishihara Sangyo Kaisha | Kemisk stabiliseret herbicidisk olie-baseret suspension |
| DE4217928A1 (de) * | 1992-05-30 | 1993-12-02 | Hoechst Ag | Neue Mischungen aus Herbiziden und Antidots, neue (Hetero-)Aryloxy-Verbindungen, Verfahren zu deren Herstellung, diese enthaltenden Mittel und deren Verwendung |
| AU6996494A (en) * | 1993-05-26 | 1994-12-20 | Sandoz Ltd. | Herbicidal compositions |
| CN1056298C (zh) * | 1996-12-31 | 2000-09-13 | 佛山市中医院 | 一种治疗软组织损伤的外用药及其生产方法 |
| AU708918B2 (en) * | 1997-01-28 | 1999-08-19 | Syngenta Participations Ag | Herbicidal synergistic composition and method of weed control |
| HUP0301968A3 (en) | 1999-11-17 | 2004-06-28 | Bayer Ag | Selective and synergistic herbicide compositions containing 2,6-disubstituted pyridine derivatives, preparation and use thereof |
| AR048414A1 (es) * | 2004-02-26 | 2006-04-26 | Ishihara Sangyo Kaisha | Composicion herbicida |
| DK1734823T3 (da) * | 2004-04-01 | 2009-08-24 | Basf Se | Synergistisk virkende herbicidblandinger |
| KR101280059B1 (ko) * | 2004-12-17 | 2013-06-28 | 주식회사 엘지생명과학 | 엔-[[(4,6-디메톡시-2-피리미디닐)아미노]카보닐]-2-[2-플루오로-1-(메톡시메틸 카보닐옥시)프로필]-3-피리딘설폰아미드를 함유하는 상승적 작용성의 제초제 조성물 |
| EP1928245B2 (en) * | 2005-09-28 | 2016-07-06 | Ishihara Sangyo Kaisha, Ltd. | Herbicidal composition |
| RU2313219C2 (ru) * | 2006-01-18 | 2007-12-27 | Государственное учреждение "Научно-исследовательский технологический институт гербицидов и регуляторов роста растений с опытно-экспериментальным производством" (НИТИГ) | Гербицидное средство и способ его получения (варианты) |
| CN102334494A (zh) * | 2011-06-20 | 2012-02-01 | 陕西韦尔奇作物保护有限公司 | 一种含烟嘧磺隆的除草组合物 |
| GB2496643B (en) * | 2011-11-17 | 2016-08-17 | Rotam Agrochem Int Co Ltd | Herbicidal suspension concentrate |
| AR089283A1 (es) | 2011-12-27 | 2014-08-13 | Ishihara Sangyo Kaisha | Composicion herbicida |
| CN104284587B (zh) * | 2012-05-08 | 2016-06-29 | 石原产业株式会社 | 除草组合物 |
| CN103210943A (zh) * | 2013-04-27 | 2013-07-24 | 北京燕化永乐农药有限公司 | 除草组合物 |
| CN104106584A (zh) * | 2014-01-26 | 2014-10-22 | 山东先达农化股份有限公司 | 一种玉米田复配除草剂组合物 |
| CN105360137A (zh) * | 2015-10-09 | 2016-03-02 | 南宁源广农业科技有限公司 | 除草剂 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IN164880B (zh) | 1986-01-30 | 1989-06-24 | Ishihara Sangyo Kaisha | |
| US4789393A (en) * | 1986-03-07 | 1988-12-06 | E. I. Du Pont De Nemours And Company | Herbicidal pyridine sulfonamides |
| ZA871590B (en) * | 1986-03-07 | 1988-11-30 | Du Pont | Herbicidal pyridine sulfonamides |
| JPH06278588A (ja) * | 1993-03-24 | 1994-10-04 | Aisin Seiki Co Ltd | 制動力制御装置 |
-
1988
- 1988-07-19 NZ NZ225473A patent/NZ225473A/xx unknown
- 1988-07-22 JP JP63181519A patent/JP2696139B2/ja not_active Expired - Lifetime
- 1988-07-27 HU HU884000A patent/HU205834B/hu unknown
- 1988-07-29 BR BR8803777A patent/BR8803777A/pt not_active IP Right Cessation
- 1988-07-29 MY MYPI88000863A patent/MY103546A/en unknown
- 1988-08-02 EP EP92112416A patent/EP0526796A2/en not_active Withdrawn
- 1988-08-02 ES ES88307127T patent/ES2052727T3/es not_active Expired - Lifetime
- 1988-08-02 DE DE3888426T patent/DE3888426T2/de not_active Expired - Lifetime
- 1988-08-02 EP EP88307127A patent/EP0303383B1/en not_active Expired - Lifetime
- 1988-08-04 AU AU20498/88A patent/AU608637B2/en not_active Expired
- 1988-08-09 CN CN88104874A patent/CN1022284C/zh not_active Expired - Lifetime
- 1988-08-09 TR TR00681/90A patent/TR28196A/xx unknown
- 1988-08-09 BG BG085185A patent/BG48092A3/xx unknown
- 1988-08-09 BG BG086838A patent/BG49812A3/xx unknown
- 1988-08-09 TR TR00592/88A patent/TR28216A/xx unknown
- 1988-08-09 EG EG433/88A patent/EG18676A/xx active
- 1988-08-09 KR KR1019880010136A patent/KR930002953B1/ko not_active Expired - Lifetime
- 1988-08-09 TR TR00680/90A patent/TR28199A/xx unknown
- 1988-08-10 US US07/230,395 patent/USH670H/en not_active Abandoned
-
1992
- 1992-11-27 LV LVP-92-220A patent/LV10019B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EG18676A (en) | 1993-10-30 |
| BG49812A3 (en) | 1992-02-14 |
| EP0526796A3 (zh) | 1994-01-26 |
| JP2696139B2 (ja) | 1998-01-14 |
| LV10019A (lv) | 1994-05-10 |
| USH670H (en) | 1989-09-05 |
| LV10019B (en) | 1995-06-20 |
| HUT49459A (en) | 1989-10-30 |
| JPH0276803A (ja) | 1990-03-16 |
| BG48092A3 (en) | 1990-11-15 |
| KR930002953B1 (ko) | 1993-04-16 |
| HU205834B (en) | 1992-07-28 |
| EP0303383B1 (en) | 1994-03-16 |
| KR890003285A (ko) | 1989-04-14 |
| AU608637B2 (en) | 1991-04-11 |
| AU2049888A (en) | 1989-02-16 |
| NZ225473A (en) | 1990-02-26 |
| EP0303383A2 (en) | 1989-02-15 |
| TR28216A (tr) | 1996-03-01 |
| CN1031174A (zh) | 1989-02-22 |
| EP0303383A3 (en) | 1991-01-16 |
| TR28196A (tr) | 1996-04-17 |
| DE3888426T2 (de) | 1994-06-23 |
| EP0526796A2 (en) | 1993-02-10 |
| TR28199A (tr) | 1996-02-13 |
| BR8803777A (pt) | 1989-02-21 |
| ES2052727T3 (es) | 1994-07-16 |
| MY103546A (en) | 1993-07-31 |
| DE3888426D1 (de) | 1994-04-21 |
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