HU187405B - Herbicidal compositions with synergic action - Google Patents
Herbicidal compositions with synergic action Download PDFInfo
- Publication number
- HU187405B HU187405B HU822712A HU271282A HU187405B HU 187405 B HU187405 B HU 187405B HU 822712 A HU822712 A HU 822712A HU 271282 A HU271282 A HU 271282A HU 187405 B HU187405 B HU 187405B
- Authority
- HU
- Hungary
- Prior art keywords
- weight
- formula
- active ingredient
- weeds
- herbicidal compositions
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 39
- 230000002195 synergetic effect Effects 0.000 title claims abstract description 21
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 9
- 125000001309 chloro group Chemical group Cl* 0.000 claims abstract description 5
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims abstract description 5
- 239000000460 chlorine Substances 0.000 claims abstract description 4
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 4
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims abstract description 4
- -1 aliphatic alcohols Chemical class 0.000 claims description 11
- 239000002904 solvent Substances 0.000 claims description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical class O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000002736 nonionic surfactant Substances 0.000 claims description 5
- 239000005995 Aluminium silicate Substances 0.000 claims description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 4
- 229920001213 Polysorbate 20 Polymers 0.000 claims description 4
- 235000012211 aluminium silicate Nutrition 0.000 claims 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 claims description 4
- 239000007788 liquid Substances 0.000 claims description 4
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 claims description 4
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 claims description 4
- ZRYCRPNCXLQHPN-UHFFFAOYSA-N 3-hydroxy-2-methylbenzaldehyde Chemical compound CC1=C(O)C=CC=C1C=O ZRYCRPNCXLQHPN-UHFFFAOYSA-N 0.000 claims description 3
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
- 239000003945 anionic surfactant Substances 0.000 claims description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 3
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- 229920005610 lignin Polymers 0.000 claims description 3
- 125000005394 methallyl group Chemical group 0.000 claims description 3
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 claims description 3
- 229920000151 polyglycol Polymers 0.000 claims description 3
- 239000010695 polyglycol Substances 0.000 claims description 3
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 3
- 239000008158 vegetable oil Substances 0.000 claims description 3
- 238000009736 wetting Methods 0.000 claims description 3
- 239000005909 Kieselgur Substances 0.000 claims description 2
- 150000008365 aromatic ketones Chemical class 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 229940071161 dodecylbenzenesulfonate Drugs 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 150000003458 sulfonic acid derivatives Chemical class 0.000 claims description 2
- 125000003363 1,3,5-triazinyl group Chemical class N1=C(N=CN=C1)* 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 abstract description 30
- 239000004480 active ingredient Substances 0.000 abstract description 27
- 150000001875 compounds Chemical class 0.000 abstract description 16
- 241000209140 Triticum Species 0.000 abstract description 13
- 235000021307 Triticum Nutrition 0.000 abstract description 12
- 230000002349 favourable effect Effects 0.000 abstract description 2
- 244000037666 field crops Species 0.000 abstract description 2
- 238000009472 formulation Methods 0.000 description 10
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 10
- FZXISNSWEXTPMF-UHFFFAOYSA-N terbutylazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C)=N1 FZXISNSWEXTPMF-UHFFFAOYSA-N 0.000 description 10
- 241001166549 Veronica hederifolia Species 0.000 description 9
- 239000004009 herbicide Substances 0.000 description 9
- BCQMBFHBDZVHKU-UHFFFAOYSA-N terbumeton Chemical compound CCNC1=NC(NC(C)(C)C)=NC(OC)=N1 BCQMBFHBDZVHKU-UHFFFAOYSA-N 0.000 description 9
- 239000005621 Terbuthylazine Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 241001621841 Alopecurus myosuroides Species 0.000 description 7
- 241001666377 Apera Species 0.000 description 7
- 235000011305 Capsella bursa pastoris Nutrition 0.000 description 7
- 240000008867 Capsella bursa-pastoris Species 0.000 description 7
- 244000151107 Triticum aestivum ssp vulgare Species 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 7
- 238000005507 spraying Methods 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 230000003042 antagnostic effect Effects 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 235000019441 ethanol Nutrition 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 240000005592 Veronica officinalis Species 0.000 description 3
- 241000405217 Viola <butterfly> Species 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000000546 pharmaceutical excipient Substances 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- 238000009331 sowing Methods 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- 241000207199 Citrus Species 0.000 description 2
- 244000042664 Matricaria chamomilla Species 0.000 description 2
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 2
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
- 244000046052 Phaseolus vulgaris Species 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 235000020971 citrus fruits Nutrition 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 235000009973 maize Nutrition 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
- 150000000182 1,3,5-triazines Chemical class 0.000 description 1
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 1
- 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 description 1
- 229910002016 Aerosil® 200 Inorganic materials 0.000 description 1
- 241000743985 Alopecurus Species 0.000 description 1
- 241000602336 Anthemis arvensis Species 0.000 description 1
- 244000251090 Anthemis cotula Species 0.000 description 1
- 235000007639 Anthemis cotula Nutrition 0.000 description 1
- 241000209134 Arundinaria Species 0.000 description 1
- 239000005476 Bentazone Substances 0.000 description 1
- 101000742062 Bos taurus Protein phosphatase 1G Proteins 0.000 description 1
- 244000024671 Brassica kaber Species 0.000 description 1
- 235000014750 Brassica kaber Nutrition 0.000 description 1
- XTFNPKDYCLFGPV-OMCISZLKSA-N Bromofenoxim Chemical compound C1=C(Br)C(O)=C(Br)C=C1\C=N\OC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O XTFNPKDYCLFGPV-OMCISZLKSA-N 0.000 description 1
- 244000157790 Buglossoides arvense Species 0.000 description 1
- 235000004256 Buglossoides arvense Nutrition 0.000 description 1
- 241001260012 Bursa Species 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 241000220244 Capsella <angiosperm> Species 0.000 description 1
- 235000005940 Centaurea cyanus Nutrition 0.000 description 1
- 240000004385 Centaurea cyanus Species 0.000 description 1
- 235000007866 Chamaemelum nobile Nutrition 0.000 description 1
- 241001327343 Chrysopogon gryllus Species 0.000 description 1
- 235000005918 Cirsium arvense Nutrition 0.000 description 1
- 240000001579 Cirsium arvense Species 0.000 description 1
- 241001503991 Consolida Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000005504 Dicamba Substances 0.000 description 1
- 239000001692 EU approved anti-caking agent Substances 0.000 description 1
- PTFJIKYUEPWBMS-UHFFFAOYSA-N Ethalfluralin Chemical compound CC(=C)CN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O PTFJIKYUEPWBMS-UHFFFAOYSA-N 0.000 description 1
- GXAMYUGOODKVRM-UHFFFAOYSA-N Flurecol Chemical compound C1=CC=C2C(C(=O)O)(O)C3=CC=CC=C3C2=C1 GXAMYUGOODKVRM-UHFFFAOYSA-N 0.000 description 1
- 244000307700 Fragaria vesca Species 0.000 description 1
- 235000016623 Fragaria vesca Nutrition 0.000 description 1
- 235000011363 Fragaria x ananassa Nutrition 0.000 description 1
- 235000014820 Galium aparine Nutrition 0.000 description 1
- 240000005702 Galium aparine Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 244000299507 Gossypium hirsutum Species 0.000 description 1
- 244000020551 Helianthus annuus Species 0.000 description 1
- 235000003222 Helianthus annuus Nutrition 0.000 description 1
- 206010061217 Infestation Diseases 0.000 description 1
- 235000009198 Lamium amplexicaule Nutrition 0.000 description 1
- 244000303225 Lamium amplexicaule Species 0.000 description 1
- 235000009193 Lamium purpureum Nutrition 0.000 description 1
- 240000006503 Lamium purpureum Species 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- 239000005574 MCPA Substances 0.000 description 1
- 241001442135 Myosotis arvensis Species 0.000 description 1
- RACGGEFQKXIDQA-UHFFFAOYSA-N N-nitro-N-[4-(trifluoromethyl)phenyl]nitramide Chemical compound [O-][N+](=O)N([N+]([O-])=O)C1=CC=C(C(F)(F)F)C=C1 RACGGEFQKXIDQA-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 235000007846 Papaver rhoeas Nutrition 0.000 description 1
- 240000004674 Papaver rhoeas Species 0.000 description 1
- 239000005591 Pendimethalin Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 235000000241 Raphanus raphanistrum Nutrition 0.000 description 1
- 244000286177 Raphanus raphanistrum Species 0.000 description 1
- 240000003728 Spergula arvensis Species 0.000 description 1
- 240000006694 Stellaria media Species 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- 235000008214 Thlaspi arvense Nutrition 0.000 description 1
- 240000008488 Thlaspi arvense Species 0.000 description 1
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 1
- 241001074087 Urophycis chuss Species 0.000 description 1
- 244000274883 Urtica dioica Species 0.000 description 1
- 235000009108 Urtica dioica Nutrition 0.000 description 1
- 235000005545 Veronica americana Nutrition 0.000 description 1
- 241000990144 Veronica persica Species 0.000 description 1
- 241001470675 Veronica polita Species 0.000 description 1
- 241000394440 Viola arvensis Species 0.000 description 1
- 235000009754 Vitis X bourquina Nutrition 0.000 description 1
- 235000012333 Vitis X labruscana Nutrition 0.000 description 1
- 240000006365 Vitis vinifera Species 0.000 description 1
- 235000014787 Vitis vinifera Nutrition 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 125000001931 aliphatic group Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 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 description 1
- CNBGNNVCVSKAQZ-UHFFFAOYSA-N benzidamine Natural products C12=CC=CC=C2C(OCCCN(C)C)=NN1CC1=CC=CC=C1 CNBGNNVCVSKAQZ-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 230000008029 eradication Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 230000003054 hormonal effect Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- PUIYMUZLKQOUOZ-UHFFFAOYSA-N isoproturon Chemical compound CC(C)C1=CC=C(NC(=O)N(C)C)C=C1 PUIYMUZLKQOUOZ-UHFFFAOYSA-N 0.000 description 1
- 230000000366 juvenile effect Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- 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 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000004476 plant protection product Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000005082 stem growth Effects 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical class OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 239000004546 suspension concentrate Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000008096 xylene 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
- A01N43/68—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms with two or three nitrogen atoms directly attached to ring carbon atoms
- A01N43/70—Diamino—1,3,5—triazines with only one oxygen, sulfur or halogen atom or only one cyano, thiocyano (—SCN), cyanato (—OCN) or azido (—N3) group directly attached to a ring carbon atom
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (19)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU822712A HU187405B (en) | 1982-08-24 | 1982-08-24 | Herbicidal compositions with synergic action |
ZA836074A ZA836074B (en) | 1982-08-24 | 1983-08-17 | Synergistic herbicidal composition |
FR8313596A FR2532152A1 (fr) | 1982-08-24 | 1983-08-23 | Composition herbicide synergique contenant des composes de types etalfluraline et terbutrine |
CS836139A CS235339B2 (en) | 1982-08-24 | 1983-08-23 | Synergic herbicide agent |
GR72278A GR78677B (cs) | 1982-08-24 | 1983-08-23 | |
CA000435131A CA1204298A (en) | 1982-08-24 | 1983-08-23 | Synergistic herbicidal composition |
AT301383A AT382294B (de) | 1982-08-24 | 1983-08-24 | Synergistische herbizide mittel |
SU833638901A SU1375110A3 (ru) | 1982-08-24 | 1983-08-24 | Гербицидное средство |
CH4695/83A CH654463A5 (de) | 1982-08-24 | 1983-08-24 | Synergetische herbizide mittel. |
AU18398/83A AU557263B2 (en) | 1982-08-24 | 1983-08-24 | Aniline etalfluralin and triazine terbumeton synergistic composition |
PL1983243510A PL135874B1 (en) | 1982-08-24 | 1983-08-24 | Synergetic herbicide |
IT22632/83A IT1163929B (it) | 1982-08-24 | 1983-08-24 | Composizione erbicida sinergica |
DD83254189A DD211471A5 (de) | 1982-08-24 | 1983-08-24 | Synergetische herbizide mittel |
ES525557A ES8606980A1 (es) | 1982-08-24 | 1983-08-24 | Procedimiento de preparar agentes herbicidas sinergicos |
JP58154746A JPS5984806A (ja) | 1982-08-24 | 1983-08-24 | 相乗性殺草組成物 |
BR8304566A BR8304566A (pt) | 1982-08-24 | 1983-08-24 | Composicao herbecida sinergistica |
GB08322697A GB2126092B (en) | 1982-08-24 | 1983-08-24 | Synergistic herbicidal composition |
DE3330546A DE3330546C2 (de) | 1982-08-24 | 1983-08-24 | Herbizide |
MN84641A MN325A8 (en) | 1982-08-24 | 1984-12-18 | Composition of synergetic herbicides |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU822712A HU187405B (en) | 1982-08-24 | 1982-08-24 | Herbicidal compositions with synergic action |
Publications (1)
Publication Number | Publication Date |
---|---|
HU187405B true HU187405B (en) | 1986-01-28 |
Family
ID=10960761
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU822712A HU187405B (en) | 1982-08-24 | 1982-08-24 | Herbicidal compositions with synergic action |
Country Status (18)
Country | Link |
---|---|
JP (1) | JPS5984806A (cs) |
AU (1) | AU557263B2 (cs) |
BR (1) | BR8304566A (cs) |
CA (1) | CA1204298A (cs) |
CH (1) | CH654463A5 (cs) |
CS (1) | CS235339B2 (cs) |
DD (1) | DD211471A5 (cs) |
DE (1) | DE3330546C2 (cs) |
ES (1) | ES8606980A1 (cs) |
FR (1) | FR2532152A1 (cs) |
GB (1) | GB2126092B (cs) |
GR (1) | GR78677B (cs) |
HU (1) | HU187405B (cs) |
IT (1) | IT1163929B (cs) |
MN (1) | MN325A8 (cs) |
PL (1) | PL135874B1 (cs) |
SU (1) | SU1375110A3 (cs) |
ZA (1) | ZA836074B (cs) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9325284D0 (en) * | 1993-12-10 | 1994-02-16 | Rhone Poulenc Agriculture | Herbicidal compositions |
US5707929A (en) * | 1995-05-08 | 1998-01-13 | Troy Chemical Corporation | Biocidal compositions comprising mixtures of haloproynyl compounds and sulfur containing triazines |
HUE040245T2 (hu) * | 2013-08-21 | 2019-02-28 | Dow Agrosciences Llc | Herbicid készítmények, amelyek szulfentrazont plusz propizamidot és szulfentrazont plusz propizamidot plusz etalfluralint tartalmaznak |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1505249A (en) * | 1974-03-23 | 1978-03-30 | Lilly Co Eli | Herbicides |
FR2414870A1 (fr) * | 1977-08-04 | 1979-08-17 | Sipcam | Composition herbicide |
IT1111151B (it) * | 1978-01-10 | 1986-01-13 | Sipcam Spa | Composizione erbicida liquida emulsionabile in acqua |
-
1982
- 1982-08-24 HU HU822712A patent/HU187405B/hu not_active IP Right Cessation
-
1983
- 1983-08-17 ZA ZA836074A patent/ZA836074B/xx unknown
- 1983-08-23 CS CS836139A patent/CS235339B2/cs unknown
- 1983-08-23 FR FR8313596A patent/FR2532152A1/fr active Pending
- 1983-08-23 GR GR72278A patent/GR78677B/el unknown
- 1983-08-23 CA CA000435131A patent/CA1204298A/en not_active Expired
- 1983-08-24 BR BR8304566A patent/BR8304566A/pt unknown
- 1983-08-24 IT IT22632/83A patent/IT1163929B/it active
- 1983-08-24 ES ES525557A patent/ES8606980A1/es not_active Expired
- 1983-08-24 PL PL1983243510A patent/PL135874B1/pl unknown
- 1983-08-24 DD DD83254189A patent/DD211471A5/de not_active IP Right Cessation
- 1983-08-24 DE DE3330546A patent/DE3330546C2/de not_active Expired
- 1983-08-24 AU AU18398/83A patent/AU557263B2/en not_active Ceased
- 1983-08-24 CH CH4695/83A patent/CH654463A5/de not_active IP Right Cessation
- 1983-08-24 JP JP58154746A patent/JPS5984806A/ja active Pending
- 1983-08-24 SU SU833638901A patent/SU1375110A3/ru active
- 1983-08-24 GB GB08322697A patent/GB2126092B/en not_active Expired
-
1984
- 1984-12-18 MN MN84641A patent/MN325A8/xx unknown
Also Published As
Publication number | Publication date |
---|---|
CA1204298A (en) | 1986-05-13 |
DD211471A5 (de) | 1984-07-18 |
IT8322632A0 (it) | 1983-08-24 |
GB2126092B (en) | 1986-04-09 |
ZA836074B (en) | 1984-07-25 |
BR8304566A (pt) | 1984-04-03 |
FR2532152A1 (fr) | 1984-03-02 |
CH654463A5 (de) | 1986-02-28 |
IT1163929B (it) | 1987-04-08 |
AU1839883A (en) | 1984-03-01 |
PL135874B1 (en) | 1985-12-31 |
JPS5984806A (ja) | 1984-05-16 |
ES8606980A1 (es) | 1986-06-01 |
CS235339B2 (en) | 1985-05-15 |
AU557263B2 (en) | 1986-12-18 |
ES525557A0 (es) | 1986-06-01 |
GB2126092A (en) | 1984-03-21 |
DE3330546C2 (de) | 1985-10-31 |
SU1375110A3 (ru) | 1988-02-15 |
DE3330546A1 (de) | 1984-03-01 |
PL243510A1 (en) | 1984-07-30 |
GB8322697D0 (en) | 1983-09-28 |
GR78677B (cs) | 1984-09-27 |
MN325A8 (en) | 1985-06-15 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
HU90 | Patent valid on 900628 | ||
HMM4 | Cancellation of final prot. due to non-payment of fee |