SK31997A3 - Herbicidal agent and method of selective controlling the growth of undesirable vegetation - Google Patents

Herbicidal agent and method of selective controlling the growth of undesirable vegetation Download PDF

Info

Publication number: SK31997A3
Authority: SK; Slovakia
Prior art keywords: acid derivative; dicamba; carbon atoms; compound; alkyl
Prior art date: 1996-03-13

Application number

SK319-97A

Other languages

English (en)

Slovak (sk)

Inventor

Reynold Chollet

Luke L Bozeman

Original Assignee

Ciba Geigy Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1996-03-13

Filing date

1997-03-11

Publication date

1997-10-08

1996-03-13 Priority claimed from GBGB9605252.7A external-priority patent/GB9605252D0/en

1997-03-11 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1997-10-08 Publication of SK31997A3 publication Critical patent/SK31997A3/sk

Links

238000000034 method Methods 0.000 title claims abstract description 24
230000012010 growth Effects 0.000 title claims description 9
239000004009 herbicide Substances 0.000 title description 7
IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims abstract description 47
239000005504 Dicamba Substances 0.000 claims abstract description 43
239000002253 acid Substances 0.000 claims abstract description 35
-1 quinolinyloxy Chemical group 0.000 claims abstract description 32
231100000674 Phytotoxicity Toxicity 0.000 claims abstract description 10
150000003839 salts Chemical group 0.000 claims abstract description 5
150000001875 compounds Chemical class 0.000 claims description 60
239000000203 mixture Substances 0.000 claims description 36
230000002363 herbicidal effect Effects 0.000 claims description 21
125000000217 alkyl group Chemical group 0.000 claims description 17
125000004432 carbon atom Chemical group C* 0.000 claims description 17
COYBRKAVBMYYSF-UHFFFAOYSA-N heptan-2-yl [(5-chloroquinolin-8-yl)oxy]acetate Chemical group C1=CN=C2C(OCC(=O)OC(C)CCCCC)=CC=C(Cl)C2=C1 COYBRKAVBMYYSF-UHFFFAOYSA-N 0.000 claims description 11
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
229910052739 hydrogen Inorganic materials 0.000 claims description 7
239000001257 hydrogen Substances 0.000 claims description 7
IRJQWZWMQCVOLA-ZBKNUEDVSA-N 2-[(z)-n-[(3,5-difluorophenyl)carbamoylamino]-c-methylcarbonimidoyl]pyridine-3-carboxylic acid Chemical compound N=1C=CC=C(C(O)=O)C=1C(/C)=N\NC(=O)NC1=CC(F)=CC(F)=C1 IRJQWZWMQCVOLA-ZBKNUEDVSA-N 0.000 claims description 6
239000011248 coating agent Substances 0.000 claims description 6
238000000576 coating method Methods 0.000 claims description 6
229910052801 chlorine Inorganic materials 0.000 claims description 4
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
229910052783 alkali metal Inorganic materials 0.000 claims description 3
125000004183 alkoxy alkyl group Chemical group 0.000 claims description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
239000000460 chlorine Substances 0.000 claims description 3
229910052731 fluorine Inorganic materials 0.000 claims description 3
125000005843 halogen group Chemical group 0.000 claims description 3
JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical group CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 claims description 3
125000003545 alkoxy group Chemical group 0.000 claims description 2
229910052736 halogen Inorganic materials 0.000 claims description 2
150000002367 halogens Chemical class 0.000 claims description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
150000007659 semicarbazones Chemical class 0.000 claims 3
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 2
230000002776 aggregation Effects 0.000 claims 2
238000004220 aggregation Methods 0.000 claims 2
125000005133 alkynyloxy group Chemical group 0.000 claims 2
239000011737 fluorine Substances 0.000 claims 2
150000002431 hydrogen Chemical class 0.000 claims 2
102100035650 Extracellular calcium-sensing receptor Human genes 0.000 claims 1
101710159793 Extracellular calcium-sensing receptor Proteins 0.000 claims 1
125000003302 alkenyloxy group Chemical group 0.000 claims 1
244000038559 crop plants Species 0.000 abstract 2
241000196324 Embryophyta Species 0.000 description 25
239000004480 active ingredient Substances 0.000 description 25
241000209140 Triticum Species 0.000 description 11
235000021307 Triticum Nutrition 0.000 description 11
238000005507 spraying Methods 0.000 description 10
208000024891 symptom Diseases 0.000 description 8
239000003085 diluting agent Substances 0.000 description 7
238000012360 testing method Methods 0.000 description 7
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
230000006378 damage Effects 0.000 description 6
238000002474 experimental method Methods 0.000 description 6
239000000843 powder Substances 0.000 description 6
239000002689 soil Substances 0.000 description 6
239000007921 spray Substances 0.000 description 6
239000004094 surface-active agent Substances 0.000 description 6
239000013543 active substance Substances 0.000 description 5
238000011156 evaluation Methods 0.000 description 5
238000009472 formulation Methods 0.000 description 5
239000008187 granular material Substances 0.000 description 5
239000007787 solid Substances 0.000 description 5
239000000126 substance Substances 0.000 description 5
235000013339 cereals Nutrition 0.000 description 4
239000008199 coating composition Substances 0.000 description 4
230000005764 inhibitory process Effects 0.000 description 4
239000007788 liquid Substances 0.000 description 4
239000002245 particle Substances 0.000 description 4
239000000546 pharmaceutical excipient Substances 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
239000004563 wettable powder Substances 0.000 description 4
HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 3
239000005995 Aluminium silicate Substances 0.000 description 3
244000025254 Cannabis sativa Species 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
241000209504 Poaceae Species 0.000 description 3
240000003829 Sorghum propinquum Species 0.000 description 3
235000011684 Sorghum saccharatum Nutrition 0.000 description 3
240000008042 Zea mays Species 0.000 description 3
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
235000002017 Zea mays subsp mays Nutrition 0.000 description 3
235000012211 aluminium silicate Nutrition 0.000 description 3
239000007900 aqueous suspension Substances 0.000 description 3
229940125904 compound 1 Drugs 0.000 description 3
235000005822 corn Nutrition 0.000 description 3
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 3
238000002156 mixing Methods 0.000 description 3
229910052708 sodium Chemical group 0.000 description 3
239000011734 sodium Chemical group 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
240000002791 Brassica napus Species 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical class CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group 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 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
241000219289 Silene Species 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
229910052918 calcium silicate Inorganic materials 0.000 description 2
239000000969 carrier Substances 0.000 description 2
238000011260 co-administration Methods 0.000 description 2
239000004495 emulsifiable concentrate Substances 0.000 description 2
125000001153 fluoro group Chemical group F* 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
239000000463 material Substances 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
210000004080 milk Anatomy 0.000 description 2
230000000885 phytotoxic effect Effects 0.000 description 2
230000008654 plant damage Effects 0.000 description 2
230000008635 plant growth Effects 0.000 description 2
230000009528 severe injury Effects 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
230000002195 synergetic effect Effects 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
230000000007 visual effect Effects 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
LDMOEFOXLIZJOW-UHFFFAOYSA-N 1-dodecanesulfonic acid Chemical compound CCCCCCCCCCCCS(O)(=O)=O LDMOEFOXLIZJOW-UHFFFAOYSA-N 0.000 description 1
PTMRDOLOEDPHLB-UHFFFAOYSA-N 2,3-dipentylphenol Chemical compound CCCCCC1=CC=CC(O)=C1CCCCC PTMRDOLOEDPHLB-UHFFFAOYSA-N 0.000 description 1
VONWPEXRCLHKRJ-UHFFFAOYSA-N 2-chloro-n-phenylacetamide Chemical class ClCC(=O)NC1=CC=CC=C1 VONWPEXRCLHKRJ-UHFFFAOYSA-N 0.000 description 1
125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 description 1
125000005916 2-methylpentyl group Chemical group 0.000 description 1
ACNUVXZPCIABEX-UHFFFAOYSA-N 3',6'-diaminospiro[2-benzofuran-3,9'-xanthene]-1-one Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(N)C=C1OC1=CC(N)=CC=C21 ACNUVXZPCIABEX-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
241000219318 Amaranthus Species 0.000 description 1
235000009328 Amaranthus caudatus Nutrition 0.000 description 1
240000001592 Amaranthus caudatus Species 0.000 description 1
244000003416 Asparagus officinalis Species 0.000 description 1
235000005340 Asparagus officinalis Nutrition 0.000 description 1
241000258957 Asteroidea Species 0.000 description 1
241001645380 Bassia scoparia Species 0.000 description 1
241000533413 Bifora radians Species 0.000 description 1
241000219198 Brassica Species 0.000 description 1
235000003351 Brassica cretica Nutrition 0.000 description 1
235000011293 Brassica napus Nutrition 0.000 description 1
235000006008 Brassica napus var napus Nutrition 0.000 description 1
240000007124 Brassica oleracea Species 0.000 description 1
235000003899 Brassica oleracea var acephala Nutrition 0.000 description 1
235000011301 Brassica oleracea var capitata Nutrition 0.000 description 1
235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 1
235000003343 Brassica rupestris Nutrition 0.000 description 1
244000157790 Buglossoides arvense Species 0.000 description 1
235000004256 Buglossoides arvense Nutrition 0.000 description 1
241000217446 Calystegia sepium Species 0.000 description 1
235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
235000011305 Capsella bursa pastoris Nutrition 0.000 description 1
240000008867 Capsella bursa-pastoris Species 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
240000004385 Centaurea cyanus Species 0.000 description 1
241000238366 Cephalopoda Species 0.000 description 1
241000421296 Cerastium arvense Species 0.000 description 1
240000006122 Chenopodium album Species 0.000 description 1
235000009344 Chenopodium album Nutrition 0.000 description 1
235000005918 Cirsium arvense Nutrition 0.000 description 1
240000001579 Cirsium arvense Species 0.000 description 1
229940126062 Compound A Drugs 0.000 description 1
241000207894 Convolvulus arvensis Species 0.000 description 1
240000008853 Datura stramonium Species 0.000 description 1
244000000626 Daucus carota Species 0.000 description 1
235000002767 Daucus carota Nutrition 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
235000009419 Fagopyrum esculentum Nutrition 0.000 description 1
240000008620 Fagopyrum esculentum Species 0.000 description 1
241001289540 Fallopia convolvulus Species 0.000 description 1
244000044980 Fumaria officinalis Species 0.000 description 1
235000006961 Fumaria officinalis Nutrition 0.000 description 1
241001508646 Galeopsis tetrahit Species 0.000 description 1
244000214240 Galinsoga parviflora Species 0.000 description 1
GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
235000003222 Helianthus annuus Nutrition 0.000 description 1
244000020551 Helianthus annuus Species 0.000 description 1
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 1
206010061217 Infestation Diseases 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
241000110847 Kochia Species 0.000 description 1
235000006761 Lapsana communis Nutrition 0.000 description 1
240000002702 Lapsana communis Species 0.000 description 1
229920001732 Lignosulfonate Polymers 0.000 description 1
241000209510 Liliopsida Species 0.000 description 1
241000058193 Lipandra polysperma Species 0.000 description 1
244000042664 Matricaria chamomilla Species 0.000 description 1
235000007232 Matricaria chamomilla Nutrition 0.000 description 1
235000010624 Medicago sativa Nutrition 0.000 description 1
240000004658 Medicago sativa Species 0.000 description 1
235000016462 Mimosa pudica Nutrition 0.000 description 1
240000001140 Mimosa pudica Species 0.000 description 1
241001442135 Myosotis arvensis Species 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241000283973 Oryctolagus cuniculus Species 0.000 description 1
235000007846 Papaver rhoeas Nutrition 0.000 description 1
240000004674 Papaver rhoeas Species 0.000 description 1
240000001090 Papaver somniferum Species 0.000 description 1
244000037751 Persicaria maculosa Species 0.000 description 1
241000719029 Polla Species 0.000 description 1
241000205407 Polygonum Species 0.000 description 1
235000006386 Polygonum aviculare Nutrition 0.000 description 1
244000292697 Polygonum aviculare Species 0.000 description 1
235000004442 Polygonum persicaria Nutrition 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
241000245063 Primula Species 0.000 description 1
235000000497 Primula Nutrition 0.000 description 1
235000016311 Primula vulgaris Nutrition 0.000 description 1
244000028344 Primula vulgaris Species 0.000 description 1
239000006004 Quartz sand Substances 0.000 description 1
241000822966 Ranunculus arvensis Species 0.000 description 1
235000009422 Rumex obtusifolius Nutrition 0.000 description 1
240000007113 Rumex obtusifolius Species 0.000 description 1
240000000111 Saccharum officinarum Species 0.000 description 1
235000007201 Saccharum officinarum Nutrition 0.000 description 1
244000124765 Salsola kali Species 0.000 description 1
241000125250 Scandix Species 0.000 description 1
240000003705 Senecio vulgaris Species 0.000 description 1
235000014846 Sisymbrium alliaria Nutrition 0.000 description 1
240000007807 Sisymbrium officinale Species 0.000 description 1
235000002974 Sisymbrium officinale Nutrition 0.000 description 1
235000002594 Solanum nigrum Nutrition 0.000 description 1
244000061457 Solanum nigrum Species 0.000 description 1
241000950790 Solanum sarrachoides Species 0.000 description 1
241000488874 Sonchus Species 0.000 description 1
235000006731 Sonchus arvensis Nutrition 0.000 description 1
244000111146 Sonchus arvensis Species 0.000 description 1
240000003728 Spergula arvensis Species 0.000 description 1
240000006694 Stellaria media Species 0.000 description 1
229940100389 Sulfonylurea Drugs 0.000 description 1
240000001949 Taraxacum officinale Species 0.000 description 1
244000042324 Trifolium repens Species 0.000 description 1
241000201338 Veronica arvensis Species 0.000 description 1
241001166549 Veronica hederifolia Species 0.000 description 1
241000990144 Veronica persica Species 0.000 description 1
241000219873 Vicia Species 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
125000005452 alkenyloxyalkyl group Chemical group 0.000 description 1
239000004178 amaranth Substances 0.000 description 1
235000012735 amaranth Nutrition 0.000 description 1
230000003042 antagnostic effect Effects 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
235000011920 black pudding Nutrition 0.000 description 1
235000009120 camo Nutrition 0.000 description 1
239000002775 capsule Substances 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
235000005607 chanvre indien Nutrition 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
230000000295 complement effect Effects 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
235000008504 concentrate Nutrition 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
239000004491 dispersible concentrate Substances 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000002552 dosage form Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
238000005187 foaming Methods 0.000 description 1
235000011389 fruit/vegetable juice Nutrition 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
229910052733 gallium Inorganic materials 0.000 description 1
238000000227 grinding Methods 0.000 description 1
239000011487 hemp Substances 0.000 description 1
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
230000000749 insecticidal effect Effects 0.000 description 1
238000007689 inspection Methods 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
210000003127 knee Anatomy 0.000 description 1
235000014666 liquid concentrate Nutrition 0.000 description 1
239000008297 liquid dosage form Substances 0.000 description 1
125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
239000003094 microcapsule Substances 0.000 description 1
235000013336 milk Nutrition 0.000 description 1
239000008267 milk Substances 0.000 description 1
230000009526 moderate injury Effects 0.000 description 1
235000010460 mustard Nutrition 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 1
230000017066 negative regulation of growth Effects 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000004806 packaging method and process Methods 0.000 description 1
239000003415 peat Substances 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Chemical group 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
229940043267 rhodamine b Drugs 0.000 description 1
238000009666 routine test Methods 0.000 description 1
238000005245 sintering Methods 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000000243 solution Substances 0.000 description 1
238000009331 sowing Methods 0.000 description 1
241000894007 species Species 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000011550 stock solution Substances 0.000 description 1
239000004575 stone Substances 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 description 1
238000004381 surface treatment Methods 0.000 description 1
239000004546 suspension concentrate Substances 0.000 description 1
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000000230 xanthan gum Substances 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1
229940082509 xanthan gum Drugs 0.000 description 1
235000010493 xanthan gum Nutrition 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
- A01N37/38—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
- A01N37/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- 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<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products

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)

SK319-97A 1996-03-13 1997-03-11 Herbicidal agent and method of selective controlling the growth of undesirable vegetation SK31997A3 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GBGB9605252.7A GB9605252D0 (en)	1996-03-13	1996-03-13	Novel combinations
US73528996A	1996-10-22	1996-10-22

Publications (1)

Publication Number	Publication Date
SK31997A3 true SK31997A3 (en)	1997-10-08

Family

ID=26308921

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK319-97A SK31997A3 (en)	1996-03-13	1997-03-11	Herbicidal agent and method of selective controlling the growth of undesirable vegetation

Country Status (15)

Country	Link
US (1)	US6090750A (cs)
EP (1)	EP0795269B1 (cs)
AR (1)	AR006183A1 (cs)
AT (1)	ATE245899T1 (cs)
AU (1)	AU1624997A (cs)
BR (1)	BR9701280A (cs)
CA (1)	CA2199651C (cs)
CZ (1)	CZ74697A3 (cs)
DE (1)	DE69723750T2 (cs)
EA (1)	EA000303B1 (cs)
ES (1)	ES2205156T3 (cs)
HU (1)	HUP9700567A1 (cs)
PL (1)	PL318875A1 (cs)
SK (1)	SK31997A3 (cs)
TR (1)	TR199700187A2 (cs)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6284711B1 (en) *	1999-12-15	2001-09-04	Basf Corporation	Use of a semicarbazone plant growth regulator for early termination of crop plants
AU2003252537A1 (en) *	2002-06-08	2003-12-22	Bayer Cropscience Gmbh	Combinations of herbicidal aromatic carboxylic acids and safeners
JP5291879B2 (ja) *	2003-03-13	2013-09-18	ビーエーエスエフソシエタス・ヨーロピア	除草剤混合物
DE10321876A1 (de) *	2003-05-15	2004-12-02	Bayer Materialscience Ag	Katalysator
BRPI0416159A (pt) *	2003-11-03	2007-01-16	Bayer Cropscience Gmbh	agente de eficácia herbicida
EP2309862A2 (en) *	2008-07-11	2011-04-20	FBSciences Holdings, Inc.	Foliarly applicable silicon nutrition compositions&methods
WO2011028975A2 (en) *	2009-09-03	2011-03-10	Floratine Biosciences, Inc.	Seed treatment compositions & methods
BR112012007613A2 (pt) *	2009-09-28	2017-06-20	Fbsciences Holdings Inc	composições e métodos fertilizantes
CN102958347B (zh) *	2009-09-28	2015-03-11	Fb科技控股公司	减少植物应激的方法
AU2011279054B2 (en)	2010-07-15	2016-02-18	Fbsciences Holdings, Inc.	Microorganism compositions and methods
WO2013106724A1 (en)	2012-01-12	2013-07-18	Fbsciences Holdings, Inc.	Modulation of plant biology
MX368746B (es)	2012-12-21	2019-10-14	Dow Agrosciences Llc	Composiciones acuosas de cloquintocet-mexilo de temperatura estable.
CA2973915C (en) *	2015-01-22	2024-01-16	BASF Agro B.V.	Ternary herbicidal combination comprising saflufenacil
US11219212B2 (en)	2015-07-10	2022-01-11	BASF Agro B.V.	Herbicidal composition comprising cinmethylin and imazamox
US12336536B2 (en)	2015-07-10	2025-06-24	BASF Agro B.V.	Method for controlling herbicide resistant or tolerant weeds
EP3319436B1 (en)	2015-07-10	2019-09-11	BASF Agro B.V.	Herbicidal composition comprising cinmethylin and quinmerac
JP6875368B2 (ja)	2015-07-10	2021-05-26	ビーエーエスエフアグロベー．ブイ．	シンメチリン及びアセトクロール又はプレチラクロールを含む除草剤組成物
WO2017009142A1 (en)	2015-07-10	2017-01-19	BASF Agro B.V.	Herbicidal composition comprising cinmethylin and specific pigment synthesis inhibitors
US11219215B2 (en)	2015-07-10	2022-01-11	BASF Agro B.V.	Herbicidal composition comprising cinmethylin and specific inhibitors of protoporphyrinogen oxidase
AU2016292399B2 (en)	2015-07-10	2020-06-25	BASF Agro B.V.	Herbicidal composition comprising cinmethylin and dimethenamid
WO2017009061A1 (en)	2015-07-10	2017-01-19	BASF Agro B.V.	Herbicidal composition comprising cinmethylin and saflufenacil
WO2017009090A1 (en)	2015-07-10	2017-01-19	BASF Agro B.V.	Herbicidal composition comprising cinmethylin and pyroxasulfone
DK3319434T3 (da)	2015-07-10	2019-07-29	Basf Agro Bv	Herbicidsammensætning, der omfatter cinmethylin og pethoxamid

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3444192A (en) *	1961-04-17	1969-05-13	Hooker Chemical Corp	Process for preparing alkoxychlorinated benzoic acids
DE2129109C3 (de) *	1971-06-11	1979-06-07	Lentia Gmbh	Phenylpyridazine, ihre Herstellung und sie enthaltende herbizide Mittel
ATE103902T1 (de) *	1982-05-07	1994-04-15	Ciba Geigy Ag	Verwendung von chinolinderivaten zum schuetzen von kulturpflanzen.
US5238604A (en) *	1987-10-05	1993-08-24	Basf Corporation	Crop oil concentrates
YU48319B (sh) *	1988-08-01	1998-05-15	Monsanto Company	Bezbednosni herbicidni derivati benzoeve kiseline
US5665673A (en) *	1988-12-29	1997-09-09	Anderson; Richard J.	Potentiating herbicidal compositions
US5484760A (en) *	1990-12-31	1996-01-16	Monsanto Company	Herbicide antidotes as safeners for reducing phytotoxicity resulting from synergistic interaction between herbicides and other pesticides
EP0646315B1 (en) *	1992-11-05	1999-05-12	Novartis AG	Novel compositions containing an auxin transport inhibitor and another herbicide
BR9406529A (pt) *	1993-05-05	1996-01-02	Victorian Chemical Internation	Adjuvantes de herbicida dessecante de colheita e desfolheante

1997
- 1997-03-04 EP EP97810122A patent/EP0795269B1/en not_active Expired - Lifetime
- 1997-03-04 AT AT97810122T patent/ATE245899T1/de not_active IP Right Cessation
- 1997-03-04 ES ES97810122T patent/ES2205156T3/es not_active Expired - Lifetime
- 1997-03-04 DE DE69723750T patent/DE69723750T2/de not_active Expired - Lifetime
- 1997-03-10 PL PL97318875A patent/PL318875A1/xx unknown
- 1997-03-10 US US08/814,946 patent/US6090750A/en not_active Expired - Lifetime
- 1997-03-11 EA EA199700022A patent/EA000303B1/ru not_active IP Right Cessation
- 1997-03-11 CZ CZ97746A patent/CZ74697A3/cs unknown
- 1997-03-11 CA CA002199651A patent/CA2199651C/en not_active Expired - Lifetime
- 1997-03-11 HU HU9700567A patent/HUP9700567A1/hu unknown
- 1997-03-11 AR ARP970100959A patent/AR006183A1/es unknown
- 1997-03-11 SK SK319-97A patent/SK31997A3/sk unknown
- 1997-03-13 TR TR97/00187A patent/TR199700187A2/xx unknown
- 1997-03-13 AU AU16249/97A patent/AU1624997A/en not_active Abandoned
- 1997-03-13 BR BR9701280A patent/BR9701280A/pt unknown

Also Published As

Publication number	Publication date
ATE245899T1 (de)	2003-08-15
AU1624997A (en)	1997-09-18
BR9701280A (pt)	1998-11-10
EA000303B1 (ru)	1999-04-29
AR006183A1 (es)	1999-08-11
CA2199651C (en)	2008-10-21
EP0795269B1 (en)	2003-07-30
HUP9700567A1 (hu)	1998-06-29
CA2199651A1 (en)	1997-09-13
US6090750A (en)	2000-07-18
DE69723750T2 (de)	2004-06-03
PL318875A1 (en)	1997-09-15
HU9700567D0 (en)	1997-04-28
ES2205156T3 (es)	2004-05-01
DE69723750D1 (de)	2003-09-04
EA199700022A1 (ru)	1997-09-30
CZ74697A3 (en)	1997-09-17
EP0795269A1 (en)	1997-09-17
TR199700187A2 (xx)	1997-10-21

Publication	Publication Date	Title
SK31997A3 (en)	1997-10-08	Herbicidal agent and method of selective controlling the growth of undesirable vegetation
RU2632860C2 (ru)	2017-10-11	Гербицидные композиции, содержащие 4-амино-3-хлор-5-фтор-6-(4-хлор-2-фтор-3-метоксифенил)пиридин-2-карбоновую кислоту или ее производное и ингибитор протопорфириногеноксидазы
RU2639885C2 (ru)	2017-12-25	Гербицидные композиции, содержащие 4-амино-3-хлор-5-фтор-6-(4-хлор-2-фтор-3-метоксифенил)пиридин-2-карбоновую кислоту или ее производное и некоторые ингибиторы ps ii
RU2632968C2 (ru)	2017-10-11	Гербицидные композиции, содержащие 4-амино-3-хлор-5-фтор-6-(4-хлор-2-фтор-3-метоксифенил)пиридин-2-карбоновую кислоту или ее производное и синтетические ауксиновые гербициды
RU2629255C2 (ru)	2017-08-28	Гербицидные композиции, содержащие 4-амино-3-хлор-5-фтор-6-(4-хлор-2-фтор-3-метоксифенил)пиридин-2-карбоновую кислоту или ее производное и гербициды, ингибирующие микротрубочки
US5236887A (en)	1993-08-17	Herbicidal heterocyclic sulfonylurea compositions safened by herbicidal acids such as 2,4-d below a ph of 5
KR20150038259A (ko)	2015-04-08	4-아미노-3-클로로-5-플루오로-6-(4-클로로-2-플루오로-3-메톡시페닐)피리딘-2-카르복실산을 포함하는 제초 조성물
JP6637408B2 (ja)	2020-01-29	ペノキシスラムおよびベンゾビシクロンまたはクロマゾンおよびベンゾビシクロンの施用からの相乗的雑草防除
KR20150038257A (ko)	2015-04-08	4-아미노-3-클로로-5-플루오로-6-(4-클로로-2-플루오로-3-메톡시페닐) 피리딘-2-카르복실산을 포함하는 제초제 조성물
RU2597191C2 (ru)	2016-09-10	Синергетическая гербицидная композиция, содержащая пеноксулам и пироксулам
KR20150038254A (ko)	2015-04-08	4-아미노-3-클로로-5-플루오로-6-(4-클로로-2-플루오로-3-메톡시페닐)피리딘-2-카르복실산을 포함하는 제초 조성물
KR20150036744A (ko)	2015-04-07	4-아미노-3-클로로-5-플루오로-6-(4-클로로-2-플루오로-3-메톡시페닐)피리딘-2-카르복실산을 포함하는 제초 조성물
KR20150036749A (ko)	2015-04-07	4-아미노-3-클로로-5-플루오로-6-(4-클로로-2-플루오로-3-메톡시페닐) 피리딘-2-카르복실산을 포함하는 제초 조성물
TW201713213A (zh)	2017-04-16	包含ｌ－固殺草及茚嗪氟草胺之殺草劑組合
KR20170139133A (ko)	2017-12-18	글루포시네이트 및 인다지플람을 포함하는 제초제 조합물
NZ584359A (en)	2011-09-30	Composisiton containing glufosinate and one of acifluorfen, oxyfluorfen and fomesafen
JP2025501193A (ja)	2025-01-17	雑草を防除するための方法
US20230082957A1 (en)	2023-03-16	Herbicidal compositions comprising fluazifop, triclopyr and diquat
CZ306295B6 (cs)	2016-11-23	Herbicidní směsi
JP5430134B2 (ja)	2014-02-26	除草剤組成物
AU654545B2 (en)	1994-11-10	Herbicidal compositions with reduced phytotoxicity
BG63766B1 (bg)	2002-12-29	Нови хербицидни, състави съдържащи 4-бензоилизоксазоли и аклонифен
EP0275556A2 (en)	1988-07-27	Herbicidal composition
MXPA97001836A (en)	1999-10-14	Herbici combinations
CN121889033A (zh)	2026-04-17	用于作物保护的新颖混合物