SK73295A3 - Selective herbicidal agent and method of selective weed suppression - Google Patents

Selective herbicidal agent and method of selective weed suppression Download PDF

Info

Publication number: SK73295A3
Authority: SK; Slovakia
Prior art keywords: alkyl; carbon atoms; group; formula; alkoxy
Prior art date: 1994-06-03

Application number

SK732-95A

Other languages

English (en)

Slovak (sk)

Inventor

Jutta Glock

Manfred Hudetz

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.)

1994-06-03

Filing date

1995-06-01

Publication date

1995-12-06

1995-06-01 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1995-12-06 Publication of SK73295A3 publication Critical patent/SK73295A3/sk

Links

239000004009 herbicide Substances 0.000 title claims abstract description 43
241000196324 Embryophyta Species 0.000 title claims abstract description 20
238000000034 method Methods 0.000 title claims description 12
230000001629 suppression Effects 0.000 title 1
125000000217 alkyl group Chemical group 0.000 claims abstract description 119
230000002363 herbicidal effect Effects 0.000 claims abstract description 44
-1 1,3-dioxan-2-yl Chemical group 0.000 claims abstract description 34
125000003545 alkoxy group Chemical group 0.000 claims abstract description 34
125000003342 alkenyl group Chemical group 0.000 claims abstract description 12
125000004104 aryloxy group Chemical group 0.000 claims abstract description 12
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims abstract description 10
125000000304 alkynyl group Chemical group 0.000 claims abstract description 10
125000001188 haloalkyl group Chemical group 0.000 claims abstract description 9
239000000654 additive Substances 0.000 claims abstract description 8
239000000969 carrier Substances 0.000 claims abstract description 8
125000003302 alkenyloxy group Chemical group 0.000 claims abstract description 7
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims abstract description 7
125000005133 alkynyloxy group Chemical group 0.000 claims abstract description 6
125000004414 alkyl thio group Chemical group 0.000 claims abstract description 5
125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 5
229910052717 sulfur Inorganic materials 0.000 claims abstract description 5
125000002947 alkylene group Chemical group 0.000 claims abstract description 4
125000006033 1,1-dimethyl-2-propenyl group Chemical group 0.000 claims abstract description 3
125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims abstract description 3
125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 3
239000005557 antagonist Substances 0.000 claims abstract description 3
125000003118 aryl group Chemical group 0.000 claims abstract description 3
125000004438 haloalkoxy group Chemical group 0.000 claims abstract description 3
125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 claims abstract 3
125000005083 alkoxyalkoxy group Chemical group 0.000 claims abstract 2
125000004432 carbon atom Chemical group C* 0.000 claims description 141
239000000203 mixture Substances 0.000 claims description 56
229910052739 hydrogen Inorganic materials 0.000 claims description 30
239000001257 hydrogen Substances 0.000 claims description 28
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 27
244000038559 crop plants Species 0.000 claims description 20
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 19
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 18
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 18
239000004480 active ingredient Substances 0.000 claims description 14
229910052736 halogen Inorganic materials 0.000 claims description 13
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 13
239000004215 Carbon black (E152) Substances 0.000 claims description 12
229910052799 carbon Inorganic materials 0.000 claims description 12
125000004093 cyano group Chemical group *C#N 0.000 claims description 12
229930195733 hydrocarbon Natural products 0.000 claims description 12
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 11
150000002367 halogens Chemical class 0.000 claims description 11
125000005843 halogen group Chemical group 0.000 claims description 9
150000002431 hydrogen Chemical class 0.000 claims description 9
240000008042 Zea mays Species 0.000 claims description 8
235000002017 Zea mays subsp mays Nutrition 0.000 claims description 8
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 8
125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 7
229910052760 oxygen Inorganic materials 0.000 claims description 7
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 7
125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 6
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 claims description 6
235000009973 maize Nutrition 0.000 claims description 6
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 5
125000004429 atom Chemical group 0.000 claims description 5
125000004430 oxygen atom Chemical group O* 0.000 claims description 4
125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 3
241000209504 Poaceae Species 0.000 claims description 3
125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 2
125000004687 alkyl sulfinyl alkyl group Chemical group 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims description 2
125000001309 chloro group Chemical group Cl* 0.000 claims description 2
125000004983 dialkoxyalkyl group Chemical group 0.000 claims description 2
125000001153 fluoro group Chemical group F* 0.000 claims description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 2
239000001301 oxygen Substances 0.000 claims description 2
125000004434 sulfur atom Chemical group 0.000 claims description 2
USVZHTBPMMSRHY-UHFFFAOYSA-N 8-[(6-bromo-1,3-benzodioxol-5-yl)sulfanyl]-9-[2-(2-chlorophenyl)ethyl]purin-6-amine Chemical compound C=1C=2OCOC=2C=C(Br)C=1SC1=NC=2C(N)=NC=NC=2N1CCC1=CC=CC=C1Cl USVZHTBPMMSRHY-UHFFFAOYSA-N 0.000 claims 5
125000003884 phenylalkyl group Chemical group 0.000 claims 3
125000002490 anilino group Chemical class [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
244000025254 Cannabis sativa Species 0.000 claims 1
150000001336 alkenes Chemical class 0.000 claims 1
125000004183 alkoxy alkyl group Chemical group 0.000 claims 1
125000004688 alkyl sulfonyl alkyl group Chemical group 0.000 claims 1
125000006350 alkyl thio alkyl group Chemical group 0.000 claims 1
150000001721 carbon Chemical group 0.000 claims 1
239000000729 antidote Substances 0.000 abstract description 35
125000005092 alkenyloxycarbonyl group Chemical group 0.000 abstract description 2
125000001475 halogen functional group Chemical group 0.000 abstract 13
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 2
125000001183 hydrocarbyl group Chemical group 0.000 abstract 2
125000003718 tetrahydrofuranyl group Chemical group 0.000 abstract 2
125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 abstract 1
150000003869 acetamides Chemical class 0.000 abstract 1
125000005108 alkenylthio group Chemical group 0.000 abstract 1
125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
125000005109 alkynylthio group Chemical group 0.000 abstract 1
125000002541 furyl group Chemical group 0.000 abstract 1
150000001875 compounds Chemical class 0.000 description 36
150000003254 radicals Chemical group 0.000 description 19
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 15
239000013543 active substance Substances 0.000 description 11
239000008187 granular material Substances 0.000 description 10
239000000843 powder Substances 0.000 description 9
239000004094 surface-active agent Substances 0.000 description 9
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 6
238000009472 formulation Methods 0.000 description 6
239000000243 solution Substances 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
235000014113 dietary fatty acids Nutrition 0.000 description 5
239000000194 fatty acid Substances 0.000 description 5
229930195729 fatty acid Natural products 0.000 description 5
150000004665 fatty acids Chemical class 0.000 description 5
238000005554 pickling Methods 0.000 description 5
239000002689 soil Substances 0.000 description 5
239000005995 Aluminium silicate Substances 0.000 description 4
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
231100000674 Phytotoxicity Toxicity 0.000 description 4
239000002202 Polyethylene glycol Substances 0.000 description 4
235000012211 aluminium silicate Nutrition 0.000 description 4
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
239000004495 emulsifiable concentrate Substances 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
229920001223 polyethylene glycol Polymers 0.000 description 4
150000003839 salts Chemical class 0.000 description 4
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 4
235000012239 silicon dioxide Nutrition 0.000 description 4
239000002904 solvent Substances 0.000 description 4
238000009331 sowing Methods 0.000 description 4
239000007921 spray Substances 0.000 description 4
239000000725 suspension Substances 0.000 description 4
GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 3
101150065749 Churc1 gene Proteins 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
102100038239 Protein Churchill Human genes 0.000 description 3
229940075522 antidotes Drugs 0.000 description 3
150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
235000019441 ethanol Nutrition 0.000 description 3
230000009931 harmful effect Effects 0.000 description 3
239000002736 nonionic surfactant Substances 0.000 description 3
239000000546 pharmaceutical excipient Substances 0.000 description 3
230000000885 phytotoxic effect Effects 0.000 description 3
229920000151 polyglycol Polymers 0.000 description 3
239000010695 polyglycol Substances 0.000 description 3
229920006395 saturated elastomer Polymers 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229920005552 sodium lignosulfonate Polymers 0.000 description 3
239000007787 solid Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
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 3
229910021532 Calcite Inorganic materials 0.000 description 2
229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
229920001214 Polysorbate 60 Polymers 0.000 description 2
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
229910052783 alkali metal Inorganic materials 0.000 description 2
150000001340 alkali metals Chemical class 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 2
150000003863 ammonium salts Chemical class 0.000 description 2
239000003945 anionic surfactant Substances 0.000 description 2
125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 description 2
239000011230 binding agent Substances 0.000 description 2
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DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
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230000035784 germination Effects 0.000 description 2
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125000001931 aliphatic group Chemical group 0.000 description 1
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239000011449 brick Substances 0.000 description 1
HKPHPIREJKHECO-UHFFFAOYSA-N butachlor Chemical compound CCCCOCN(C(=O)CCl)C1=C(CC)C=CC=C1CC HKPHPIREJKHECO-UHFFFAOYSA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
235000019864 coconut oil Nutrition 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
238000013270 controlled release Methods 0.000 description 1
125000000392 cycloalkenyl group Chemical group 0.000 description 1
239000003599 detergent Substances 0.000 description 1
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
WCGGWVOVFQNRRS-UHFFFAOYSA-N dichloroacetamide Chemical class NC(=O)C(Cl)Cl WCGGWVOVFQNRRS-UHFFFAOYSA-N 0.000 description 1
GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical class CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
239000000975 dye Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
150000005452 ethyl sulfates Chemical class 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
239000008098 formaldehyde solution Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
150000004820 halides Chemical class 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
150000002430 hydrocarbons Chemical group 0.000 description 1
125000002768 hydroxyalkyl group Chemical group 0.000 description 1
238000005286 illumination Methods 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000012669 liquid formulation Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
STEPQTYSZVCJPV-UHFFFAOYSA-N metazachlor Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)CN1N=CC=C1 STEPQTYSZVCJPV-UHFFFAOYSA-N 0.000 description 1
150000005451 methyl sulfates Chemical class 0.000 description 1
239000003094 microcapsule Substances 0.000 description 1
235000019713 millet Nutrition 0.000 description 1
239000011707 mineral Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
125000005186 naphthyloxy group Chemical group C1(=CC=CC2=CC=CC=C12)O* 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
UYDLBVPAAFVANX-UHFFFAOYSA-N octylphenoxy polyethoxyethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCO)C=C1 UYDLBVPAAFVANX-UHFFFAOYSA-N 0.000 description 1
150000002888 oleic acid derivatives Chemical class 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003904 phospholipids Chemical class 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
150000003021 phthalic acid derivatives Chemical class 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
159000000001 potassium salts Chemical class 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
239000008262 pumice Substances 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
239000004576 sand Substances 0.000 description 1
150000004671 saturated fatty acids Chemical class 0.000 description 1
235000003441 saturated fatty acids Nutrition 0.000 description 1
229910052624 sepiolite Inorganic materials 0.000 description 1
235000019355 sepiolite Nutrition 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
PYODKQIVQIVELM-UHFFFAOYSA-M sodium;2,3-bis(2-methylpropyl)naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CC(C)C)C(CC(C)C)=CC2=C1 PYODKQIVQIVELM-UHFFFAOYSA-M 0.000 description 1
235000019337 sorbitan trioleate Nutrition 0.000 description 1
229960000391 sorbitan trioleate Drugs 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
235000020354 squash Nutrition 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000008117 stearic acid Chemical class 0.000 description 1
239000004575 stone Substances 0.000 description 1
239000003760 tallow Substances 0.000 description 1
239000004753 textile Substances 0.000 description 1
150000004670 unsaturated fatty acids Chemical class 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1
150000003738 xylenes Chemical class 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
- A01N37/18—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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions

Landscapes

Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Environmental Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Zoology (AREA)
Plant Pathology (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Separation Of Suspended Particles By Flocculating Agents (AREA)
Steroid Compounds (AREA)
Semiconductor Lasers (AREA)
Catching Or Destruction (AREA)

SK732-95A 1994-06-03 1995-06-01 Selective herbicidal agent and method of selective weed suppression SK73295A3 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
CH175894		1994-06-03
CH225394		1994-07-14

Publications (1)

Publication Number	Publication Date
SK73295A3 true SK73295A3 (en)	1995-12-06

Family

ID=25688580

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK732-95A SK73295A3 (en)	1994-06-03	1995-06-01	Selective herbicidal agent and method of selective weed suppression

Country Status (32)

Country	Link
US (2)	US6569806B1 (ro)
EP (1)	EP0685157B1 (ro)
JP (2)	JPH07330506A (ro)
KR (1)	KR100350329B1 (ro)
CN (1)	CN1101647C (ro)
AT (1)	ATE179570T1 (ro)
AU (1)	AU704019B2 (ro)
BG (1)	BG61747B1 (ro)
BR (1)	BR9502648A (ro)
CA (1)	CA2150781A1 (ro)
CO (1)	CO4410276A1 (ro)
CZ (1)	CZ288339B6 (ro)
DE (1)	DE59505814D1 (ro)
EE (1)	EE9500018A (ro)
ES (1)	ES2133702T3 (ro)
FI (1)	FI952651A7 (ro)
GR (1)	GR3030624T3 (ro)
HR (1)	HRP950287B1 (ro)
HU (1)	HU216970B (ro)
IL (1)	IL113965A (ro)
LV (1)	LV11247B (ro)
NO (1)	NO952203L (ro)
NZ (1)	NZ272257A (ro)
PL (1)	PL181415B1 (ro)
RO (1)	RO111406B1 (ro)
RU (1)	RU2150833C1 (ro)
SI (1)	SI0685157T1 (ro)
SK (1)	SK73295A3 (ro)
SV (1)	SV1995000025A (ro)
TN (1)	TNSN95064A1 (ro)
UA (1)	UA46700C2 (ro)
ZA (1)	ZA954553B (ro)

Families Citing this family (5)

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PL186631B1 (pl) *	1996-03-15	2004-02-27	Syngenta Participations Ag	Synergistyczna kompozycja herbicydowa oraz sposóbzwalczania niepożądanych roślin
AR036047A1 (es) *	2001-06-13	2004-08-04	Syngenta Participations Ag	Composicion herbicida selectiva y metodo para controlar selectivamente malezas y pastos en cultivos de plantas utiles
UA78326C2 (uk) *	2002-06-12	2007-03-15	Сінгента Партісіпейшнс Аг	Гербіцидна синергетична композиція та спосіб боротьби з ростом небажаної рослинності
KR101444776B1 (ko)	2007-11-14	2014-09-30	엘지디스플레이 주식회사	액정표시장치의 제조방법
RU2473201C2 (ru) *	2011-04-19	2013-01-27	Государственное научное учреждение Чеченский научно-исследовательский институт сельского хозяйства Российской академии сельскохозяйственных наук	Способ возделывания кукурузы

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CH640108A5 (de)	1978-02-06	1983-12-30	Nitrokemia Ipartelepek	Unkrautvernichtungsmittel.
DE2948535A1 (de)	1979-12-03	1981-06-25	Basf Ag, 6700 Ludwigshafen	Dichloracetamide, herbizide mittel, die acetanilide als herbizide wirkstoffe und diese dichloracetamide als antagonistische mittel enthalten, sowie ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses
DE2930452A1 (de)	1979-07-26	1981-02-26	Bayer Ag	N,n'-bis-(halogenacyl)-diaza-cycloalkane zum schutz von kulturpflanzen vor schaedigungen durch herbizide
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HU187284B (en)	1980-12-11	1985-12-28	Mta Koezponti Kemiai Kutato In	Herbicide compositions containing antitoxines of aldehyde- and ketone-derivatives
EP0077755B1 (de) *	1981-10-16	1985-03-06	Ciba-Geigy Ag	Optisch aktives N-(1'-Methyl-2'-methoxyäthyl)-N-chloracetyl-2-äthyl-6-methylanilin als Herbizid
BR8206082A (pt) *	1981-10-20	1983-09-13	Sipcam	Composicao herbicida seletiva para milho e sorgo,processo para a fabricacao e processo para aplicacao
US4579691A (en)	1983-04-21	1986-04-01	Ciba-Geigy Corporation	Haloacylaminoalkylphosphonates
US4734119A (en)	1983-11-15	1988-03-29	Ciba-Geigy Corporation	Novel phosphorus compounds for protecting cultivated plants from the phytotoxic action of herbicides
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US4601745A (en) *	1983-12-12	1986-07-22	Ciba-Geigy Corporation	Composition for the protection of cultivated plants against the phytotoxic action of herbicides
EP0163607B1 (de)	1984-05-28	1989-11-08	Ciba-Geigy Ag	Mittel zum Schützen von Kulturpflanzen vor der phytotoxischen Wirkung von herbizid wirksamen Chloracetaniliden
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DE3600903A1 (de) *	1986-01-15	1987-07-16	Basf Ag	Optisch aktive diazabicycloalkanderivate, ein verfahren zu ihrer herstellung und ihre verwendung zum schutz von kulturpflanzen vor der phytotoxischen wirkung von herbiziden
US4740224A (en) *	1986-01-17	1988-04-26	Manville Corporation	Terminal connection for fiber glass bushing
US4846880A (en)	1986-12-15	1989-07-11	Monsanto Company	2-(Dichloroacetyl)-3-substituted-1,2,3,4-tetrahydroisoquinolines as herbicide antidotes
US5256625A (en)	1987-08-13	1993-10-26	Monsanto Company	Safening imidazolinone herbicides
US5225570A (en)	1987-08-13	1993-07-06	Monsanto Company	5-heterocyclic-substituted oxazolidine dihaloacetamides
US5256626A (en) *	1987-08-13	1993-10-26	Monsanto Company	Herbicidal compositions safened by 5-heterocyclic-substituted oxazolidine dihaloacetamides compounds
UA63884C2 (en) *	1995-04-12	2004-02-16	Singenta Participations Ag	Herbicidal composition and a method of controlling the emergence of undesirable plants
US6159899A (en)	1996-03-15	2000-12-12	Novartis Crop Protection, Inc.	Herbicidal composition and method of weed control
PL186631B1 (pl)	1996-03-15	2004-02-27	Syngenta Participations Ag	Synergistyczna kompozycja herbicydowa oraz sposóbzwalczania niepożądanych roślin

1995
- 1995-05-11 EE EE9500018A patent/EE9500018A/xx unknown
- 1995-05-15 HR HR02253/94-8A patent/HRP950287B1/xx not_active IP Right Cessation
- 1995-05-24 CO CO95022351A patent/CO4410276A1/es unknown
- 1995-05-26 DE DE59505814T patent/DE59505814D1/de not_active Expired - Lifetime
- 1995-05-26 SI SI9530252T patent/SI0685157T1/xx unknown
- 1995-05-26 EP EP95810351A patent/EP0685157B1/de not_active Expired - Lifetime
- 1995-05-26 AT AT95810351T patent/ATE179570T1/de active
- 1995-05-26 ES ES95810351T patent/ES2133702T3/es not_active Expired - Lifetime
- 1995-05-29 PL PL95308822A patent/PL181415B1/pl not_active IP Right Cessation
- 1995-05-31 FI FI952651A patent/FI952651A7/fi not_active Application Discontinuation
- 1995-05-31 BG BG99687A patent/BG61747B1/bg unknown
- 1995-05-31 NZ NZ272257A patent/NZ272257A/en not_active IP Right Cessation
- 1995-06-01 SK SK732-95A patent/SK73295A3/sk unknown
- 1995-06-01 TN TNTNSN95064A patent/TNSN95064A1/fr unknown
- 1995-06-01 UA UA95062613A patent/UA46700C2/uk unknown
- 1995-06-01 CN CN95106607A patent/CN1101647C/zh not_active Expired - Fee Related
- 1995-06-01 CZ CZ19951420A patent/CZ288339B6/cs not_active IP Right Cessation
- 1995-06-01 CA CA002150781A patent/CA2150781A1/en not_active Abandoned
- 1995-06-01 IL IL11396595A patent/IL113965A/xx not_active IP Right Cessation
- 1995-06-01 AU AU20451/95A patent/AU704019B2/en not_active Ceased
- 1995-06-02 LV LVP-95-149A patent/LV11247B/lv unknown
- 1995-06-02 BR BR9502648A patent/BR9502648A/pt not_active IP Right Cessation
- 1995-06-02 ZA ZA954553A patent/ZA954553B/xx unknown
- 1995-06-02 HU HU9501629A patent/HU216970B/hu unknown
- 1995-06-02 RO RO95-01086A patent/RO111406B1/ro unknown
- 1995-06-02 KR KR1019950014578A patent/KR100350329B1/ko not_active Expired - Lifetime
- 1995-06-02 SV SV1995000025A patent/SV1995000025A/es unknown
- 1995-06-02 RU RU95108871/04A patent/RU2150833C1/ru not_active IP Right Cessation
- 1995-06-02 NO NO952203A patent/NO952203L/no unknown
- 1995-06-05 JP JP7161418A patent/JPH07330506A/ja active Pending
1997
- 1997-03-17 US US08/819,014 patent/US6569806B1/en not_active Expired - Lifetime
1999
- 1999-06-30 GR GR990401710T patent/GR3030624T3/el unknown
2003
- 2003-05-22 US US10/443,628 patent/US20030224937A1/en not_active Abandoned
2006
- 2006-11-09 JP JP2006304605A patent/JP2007063290A/ja active Pending

Also Published As

Publication number	Publication date
EP0685157B1 (de)	1999-05-06
AU2045195A (en)	1995-12-14
BG61747B1 (bg)	1998-05-29
KR100350329B1 (ko)	2002-11-05
CZ288339B6 (en)	2001-05-16
CN1101647C (zh)	2003-02-19
RU2150833C1 (ru)	2000-06-20
RU95108871A (ru)	1997-05-10
DE59505814D1 (de)	1999-06-10
JP2007063290A (ja)	2007-03-15
IL113965A0 (en)	1995-10-31
EE9500018A (et)	1995-12-15
IL113965A (en)	1999-04-11
BG99687A (bg)	1995-12-29
CN1113410A (zh)	1995-12-20
ATE179570T1 (de)	1999-05-15
NO952203L (no)	1995-12-04
JPH07330506A (ja)	1995-12-19
KR960000026A (ko)	1996-01-25
US20030224937A1 (en)	2003-12-04
AU704019B2 (en)	1999-04-15
SI0685157T1 (en)	1999-08-31
LV11247B (en)	1996-10-20
FI952651A0 (fi)	1995-05-31
ZA954553B (en)	1995-12-04
HUT71509A (en)	1995-12-28
HU216970B (hu)	1999-10-28
RO111406B1 (ro)	1996-10-31
HRP950287A2 (en)	1997-06-30
CA2150781A1 (en)	1995-12-04
UA46700C2 (uk)	2002-06-17
US6569806B1 (en)	2003-05-27
PL308822A1 (en)	1995-12-11
NZ272257A (en)	1997-01-29
TNSN95064A1 (fr)	1996-02-06
EP0685157A1 (de)	1995-12-06
SV1995000025A (es)	1996-01-10
HU9501629D0 (en)	1995-07-28
CZ142095A3 (en)	1995-12-13
ES2133702T3 (es)	1999-09-16
HRP950287B1 (en)	1999-12-31
NO952203D0 (no)	1995-06-02
FI952651A7 (fi)	1995-12-04
LV11247A (lv)	1996-06-20
BR9502648A (pt)	1996-04-09
CO4410276A1 (es)	1997-01-09
PL181415B1 (pl)	2001-07-31
GR3030624T3 (en)	1999-10-29

Publication	Publication Date	Title
EP0268554A2 (de)	1988-05-25	1,5-Diphenylpyrazol-3-carbonsäurederivate zum Schützen von Kulturpflanzen
AU662581B2 (en)	1995-09-07	Combinations of herbicides and crop-protecting substances
JPH03291202A (ja)	1991-12-20	除草組成物
JP3350779B2 (ja)	2002-11-25	除草性相乗性組成物および雑草を防除する方法
EA009211B1 (ru)	2007-12-28	Синергические гербицидные средства, содержащие гербициды из группы бензоилпиразолов
CS235315B2 (en)	1985-05-15	Cultural plants protection agent and method of efficient substances production
SK73295A3 (en)	1995-12-06	Selective herbicidal agent and method of selective weed suppression
AU1127999A (en)	1999-12-09	Herbicidal composition
NZ245130A (en)	1994-09-27	Herbicides containing 5-(2,4,6-trimethylphenyl)-2-[1-(ethoximino)propionyl]- cyclohexane-1,3-dione and a phenoxypropionic acid ester derivative
JPH0687706A (ja)	1994-03-29	相乗的除草剤および毒性緩和剤
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