DD210832A5 - Verfahren zum schuetzen von kulturpflanzen gegen schaedigende wirkungen von agrarchemikalien - Google Patents

Verfahren zum schuetzen von kulturpflanzen gegen schaedigende wirkungen von agrarchemikalien Download PDF

Info

Publication number: DD210832A5
Authority: DD; German Democratic Republic
Prior art keywords: substituted; unsubstituted; alkyl; group; halogen
Prior art date: 1982-05-07

Application number

DD83250660A

Other languages

German (de)

English (en)

Inventor

Adolf Hubele

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.)

1982-05-07

Filing date

1983-05-05

Publication date

1984-06-27

1983-05-05 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1984-06-27 Publication of DD210832A5 publication Critical patent/DD210832A5/de

Links

238000000034 method Methods 0.000 title claims abstract description 56
239000003905 agrochemical Substances 0.000 title claims abstract description 28
230000000254 damaging effect Effects 0.000 title claims description 5
239000001257 hydrogen Substances 0.000 claims abstract description 185
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 185
-1 mercaptocarbonyl group Chemical group 0.000 claims abstract description 164
229910052736 halogen Inorganic materials 0.000 claims abstract description 148
150000002367 halogens Chemical class 0.000 claims abstract description 147
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 100
125000000217 alkyl group Chemical group 0.000 claims abstract description 80
125000003545 alkoxy group Chemical group 0.000 claims abstract description 57
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 52
125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 45
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 18
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 15
125000001931 aliphatic group Chemical group 0.000 claims abstract description 9
229930195734 saturated hydrocarbon Chemical group 0.000 claims abstract description 5
125000002015 acyclic group Chemical group 0.000 claims abstract description 4
125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 claims abstract description 4
239000000460 chlorine Substances 0.000 claims description 283
150000001875 compounds Chemical class 0.000 claims description 199
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 76
229910052801 chlorine Inorganic materials 0.000 claims description 71
239000004009 herbicide Substances 0.000 claims description 68
230000002363 herbicidal effect Effects 0.000 claims description 59
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 54
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 52
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 47
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 43
125000004430 oxygen atom Chemical group O* 0.000 claims description 41
241000196324 Embryophyta Species 0.000 claims description 39
229920006395 saturated elastomer Polymers 0.000 claims description 38
125000005842 heteroatom Chemical group 0.000 claims description 36
229910052740 iodine Inorganic materials 0.000 claims description 34
239000000203 mixture Substances 0.000 claims description 33
125000003342 alkenyl group Chemical group 0.000 claims description 30
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 30
125000000623 heterocyclic group Chemical group 0.000 claims description 30
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 29
229910052757 nitrogen Inorganic materials 0.000 claims description 28
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 27
150000003839 salts Chemical class 0.000 claims description 27
125000004433 nitrogen atom Chemical group N* 0.000 claims description 25
239000002253 acid Substances 0.000 claims description 23
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical class C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 22
125000000753 cycloalkyl group Chemical group 0.000 claims description 22
125000001309 chloro group Chemical group Cl* 0.000 claims description 21
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 21
YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical group O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims description 20
125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 20
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 20
229910052794 bromium Inorganic materials 0.000 claims description 20
229910052760 oxygen Inorganic materials 0.000 claims description 20
229910052783 alkali metal Inorganic materials 0.000 claims description 19
229910052727 yttrium Inorganic materials 0.000 claims description 19
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 18
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 16
150000003254 radicals Chemical class 0.000 claims description 16
125000001424 substituent group Chemical group 0.000 claims description 16
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 15
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 15
239000003795 chemical substances by application Substances 0.000 claims description 15
125000004663 dialkyl amino group Chemical group 0.000 claims description 15
229910052717 sulfur Inorganic materials 0.000 claims description 15
125000000304 alkynyl group Chemical group 0.000 claims description 14
125000003277 amino group Chemical group 0.000 claims description 14
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 13
230000009931 harmful effect Effects 0.000 claims description 13
125000001624 naphthyl group Chemical group 0.000 claims description 13
125000001453 quaternary ammonium group Chemical group 0.000 claims description 13
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 12
150000001340 alkali metals Chemical class 0.000 claims description 12
244000038559 crop plants Species 0.000 claims description 12
JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 12
229910052751 metal Chemical class 0.000 claims description 10
239000002184 metal Chemical class 0.000 claims description 10
125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 10
239000000654 additive Substances 0.000 claims description 9
125000005122 aminoalkylamino group Chemical group 0.000 claims description 9
150000001768 cations Chemical class 0.000 claims description 9
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 9
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 8
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 8
125000004414 alkyl thio group Chemical group 0.000 claims description 8
230000000694 effects Effects 0.000 claims description 8
125000004438 haloalkoxy group Chemical group 0.000 claims description 8
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 8
239000011630 iodine Substances 0.000 claims description 8
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 8
125000000547 substituted alkyl group Chemical group 0.000 claims description 8
XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Substances CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 7
DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 claims description 7
125000004183 alkoxy alkyl group Chemical group 0.000 claims description 7
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims description 7
125000001188 haloalkyl group Chemical group 0.000 claims description 7
CPEONABTMRSIKA-UHFFFAOYSA-N 1,4$l^{2}-oxazinane Chemical compound C1COCC[N]1 CPEONABTMRSIKA-UHFFFAOYSA-N 0.000 claims description 6
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 6
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 6
125000003282 alkyl amino group Chemical group 0.000 claims description 6
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 6
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 6
YUDRVAHLXDBKSR-UHFFFAOYSA-N [CH]1CCCCC1 Chemical compound [CH]1CCCCC1 YUDRVAHLXDBKSR-UHFFFAOYSA-N 0.000 claims description 5
125000001246 bromo group Chemical group Br* 0.000 claims description 5
125000002541 furyl group Chemical group 0.000 claims description 5
125000005191 hydroxyalkylamino group Chemical group 0.000 claims description 5
125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 5
125000003718 tetrahydrofuranyl group Chemical group 0.000 claims description 5
125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 4
229910052799 carbon Inorganic materials 0.000 claims description 4
150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 4
125000005113 hydroxyalkoxy group Chemical group 0.000 claims description 4
125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 claims description 3
125000002883 imidazolyl group Chemical group 0.000 claims description 3
239000001301 oxygen Substances 0.000 claims description 3
125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 2
WYYFNMXLUUHRAU-UHFFFAOYSA-N 2-phenoxy-2-pyridin-2-yloxypropanoic acid Chemical class C=1C=CC=NC=1OC(C(O)=O)(C)OC1=CC=CC=C1 WYYFNMXLUUHRAU-UHFFFAOYSA-N 0.000 claims description 2
239000012876 carrier material Substances 0.000 claims description 2
MJPPGVVIDGQOQT-UHFFFAOYSA-N 2-bromo-5-(2-bromo-2-nitroethenyl)furan Chemical compound [O-][N+](=O)C(Br)=CC1=CC=C(Br)O1 MJPPGVVIDGQOQT-UHFFFAOYSA-N 0.000 claims 14
229940077464 ammonium ion Drugs 0.000 claims 13
125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims 2
125000004429 atom Chemical group 0.000 claims 2
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 2
150000007970 thio esters Chemical group 0.000 claims 2
125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims 1
125000006699 (C1-C3) hydroxyalkyl group Chemical group 0.000 claims 1
125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims 1
125000006619 (C1-C6) dialkylamino group Chemical group 0.000 claims 1
125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 1
125000004754 (C2-C12) dialkylamino group Chemical group 0.000 claims 1
VOXZDWNPVJITMN-ZBRFXRBCSA-N 17β-estradiol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 VOXZDWNPVJITMN-ZBRFXRBCSA-N 0.000 claims 1
IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical class C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 claims 1
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 1
125000006725 C1-C10 alkenyl group Chemical group 0.000 claims 1
125000004399 C1-C4 alkenyl group Chemical group 0.000 claims 1
244000228957 Ferula foetida Species 0.000 claims 1
DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical group NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 claims 1
229910052770 Uranium Inorganic materials 0.000 claims 1
SYKNUAWMBRIEKB-UHFFFAOYSA-N [Cl].[Br] Chemical compound [Cl].[Br] SYKNUAWMBRIEKB-UHFFFAOYSA-N 0.000 claims 1
125000005741 alkyl alkenyl group Chemical group 0.000 claims 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
125000000392 cycloalkenyl group Chemical group 0.000 claims 1
239000004744 fabric Substances 0.000 claims 1
ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 claims 1
229940028332 halog Drugs 0.000 claims 1
125000006289 hydroxybenzyl group Chemical group 0.000 claims 1
125000005350 hydroxycycloalkyl group Chemical group 0.000 claims 1
239000004476 plant protection product Substances 0.000 claims 1
125000000446 sulfanediyl group Chemical group *S* 0.000 claims 1
150000005326 tetrahydropyrimidines Chemical class 0.000 claims 1
125000003944 tolyl group Chemical group 0.000 claims 1
DNYWZCXLKNTFFI-UHFFFAOYSA-N uranium Chemical compound [U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U] DNYWZCXLKNTFFI-UHFFFAOYSA-N 0.000 claims 1
239000000126 substance Substances 0.000 abstract description 23
239000013543 active substance Substances 0.000 abstract description 13
229940027991 antiseptic and disinfectant quinoline derivative Drugs 0.000 abstract description 8
230000002939 deleterious effect Effects 0.000 abstract description 2
125000002943 quinolinyl group Chemical class N1=C(C=CC2=CC=CC=C12)* 0.000 abstract 1
239000000729 antidote Substances 0.000 description 61
150000002431 hydrogen Chemical class 0.000 description 49
239000002689 soil Substances 0.000 description 36
239000004480 active ingredient Substances 0.000 description 21
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 15
238000002360 preparation method Methods 0.000 description 15
241000209094 Oryza Species 0.000 description 14
235000007164 Oryza sativa Nutrition 0.000 description 14
235000009566 rice Nutrition 0.000 description 14
230000001681 protective effect Effects 0.000 description 13
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 12
125000005843 halogen group Chemical group 0.000 description 11
239000004033 plastic Substances 0.000 description 11
229920003023 plastic Polymers 0.000 description 11
239000000243 solution Substances 0.000 description 11
239000008187 granular material Substances 0.000 description 10
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
235000021307 Triticum Nutrition 0.000 description 9
241000209140 Triticum Species 0.000 description 9
239000000839 emulsion Substances 0.000 description 9
239000011734 sodium Substances 0.000 description 9
239000005995 Aluminium silicate Substances 0.000 description 8
235000012211 aluminium silicate Nutrition 0.000 description 8
235000013877 carbamide Nutrition 0.000 description 8
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 8
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
239000002585 base Substances 0.000 description 7
239000012141 concentrate Substances 0.000 description 7
235000008504 concentrate Nutrition 0.000 description 7
235000014113 dietary fatty acids Nutrition 0.000 description 7
239000000194 fatty acid Substances 0.000 description 7
229930195729 fatty acid Natural products 0.000 description 7
239000011521 glass Substances 0.000 description 7
150000003248 quinolines Chemical class 0.000 description 7
238000009331 sowing Methods 0.000 description 7
239000004094 surface-active agent Substances 0.000 description 7
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
229910052784 alkaline earth metal Inorganic materials 0.000 description 6
150000001342 alkaline earth metals Chemical class 0.000 description 6
150000001408 amides Chemical class 0.000 description 6
239000004202 carbamide Substances 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 6
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
239000000843 powder Substances 0.000 description 6
FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 5
244000068988 Glycine max Species 0.000 description 5
235000010469 Glycine max Nutrition 0.000 description 5
239000002202 Polyethylene glycol Substances 0.000 description 5
239000003513 alkali Substances 0.000 description 5
150000002148 esters Chemical class 0.000 description 5
238000009472 formulation Methods 0.000 description 5
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229920001223 polyethylene glycol Polymers 0.000 description 5
239000007787 solid Substances 0.000 description 5
239000002904 solvent Substances 0.000 description 5
UENGBOCGGKLVJJ-UHFFFAOYSA-N 2-chloro-1-(2,4-difluorophenyl)ethanone Chemical compound FC1=CC=C(C(=O)CCl)C(F)=C1 UENGBOCGGKLVJJ-UHFFFAOYSA-N 0.000 description 4
IGFHQQFPSIBGKE-UHFFFAOYSA-N 4-nonylphenol Chemical compound CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 4
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 4
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 4
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 4
239000011230 binding agent Substances 0.000 description 4
150000004657 carbamic acid derivatives Chemical class 0.000 description 4
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239000011248 coating agent Substances 0.000 description 4
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150000002170 ethers Chemical class 0.000 description 4
150000004665 fatty acids Chemical class 0.000 description 4
239000007788 liquid Substances 0.000 description 4
239000002736 nonionic surfactant Substances 0.000 description 4
229910052708 sodium Inorganic materials 0.000 description 4
239000008096 xylene Substances 0.000 description 4
VONWPEXRCLHKRJ-UHFFFAOYSA-N 2-chloro-n-phenylacetamide Chemical class ClCC(=O)NC1=CC=CC=C1 VONWPEXRCLHKRJ-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
241000251730 Chondrichthyes Species 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
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 3
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MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
229910019142 PO4 Inorganic materials 0.000 description 3
240000006394 Sorghum bicolor Species 0.000 description 3
235000011684 Sorghum saccharatum Nutrition 0.000 description 3
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
240000008042 Zea mays Species 0.000 description 3
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150000007513 acids Chemical class 0.000 description 3
229940075522 antidotes Drugs 0.000 description 3
125000003118 aryl group Chemical group 0.000 description 3
239000011575 calcium Substances 0.000 description 3
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125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 3
239000000969 carrier Substances 0.000 description 3
239000003240 coconut oil Substances 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical group OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
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238000010790 dilution Methods 0.000 description 3
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229910052731 fluorine Inorganic materials 0.000 description 3
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RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
239000011133 lead Substances 0.000 description 3
238000002156 mixing Methods 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
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239000005621 Terbuthylazine Substances 0.000 description 1
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235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
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SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
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DSRNRYQBBJQVCW-UHFFFAOYSA-N metoxuron Chemical compound COC1=CC=C(NC(=O)N(C)C)C=C1Cl DSRNRYQBBJQVCW-UHFFFAOYSA-N 0.000 description 1
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XITQUSLLOSKDTB-UHFFFAOYSA-N nitrofen Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C(Cl)C=C1Cl XITQUSLLOSKDTB-UHFFFAOYSA-N 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
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239000010452 phosphate Substances 0.000 description 1
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230000000704 physical effect Effects 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
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239000011591 potassium Substances 0.000 description 1
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LFULEKSKNZEWOE-UHFFFAOYSA-N propanil Chemical compound CCC(=O)NC1=CC=C(Cl)C(Cl)=C1 LFULEKSKNZEWOE-UHFFFAOYSA-N 0.000 description 1
239000011814 protection agent Substances 0.000 description 1
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HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
SBYHFKPVCBCYGV-UHFFFAOYSA-N quinuclidine Chemical compound C1CC2CCN1CC2 SBYHFKPVCBCYGV-UHFFFAOYSA-N 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
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230000002786 root growth Effects 0.000 description 1
150000004671 saturated fatty acids Chemical class 0.000 description 1
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235000019355 sepiolite Nutrition 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
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239000004332 silver Substances 0.000 description 1
MGLWZSOBALDPEK-UHFFFAOYSA-N simetryn Chemical compound CCNC1=NC(NCC)=NC(SC)=N1 MGLWZSOBALDPEK-UHFFFAOYSA-N 0.000 description 1
239000000344 soap Substances 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
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235000011152 sodium sulphate Nutrition 0.000 description 1
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235000012424 soybean oil Nutrition 0.000 description 1
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241000894007 species Species 0.000 description 1
239000007921 spray Substances 0.000 description 1
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150000003460 sulfonic acids Chemical class 0.000 description 1
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230000008961 swelling Effects 0.000 description 1
239000003760 tallow Substances 0.000 description 1
ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 1
QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
239000004753 textile Substances 0.000 description 1
229940124597 therapeutic agent Drugs 0.000 description 1
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238000005809 transesterification reaction Methods 0.000 description 1
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150000003624 transition metals Chemical class 0.000 description 1
YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
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GETQZCLCWQTVFV-UHFFFAOYSA-O trimethylammonium Chemical compound C[NH+](C)C GETQZCLCWQTVFV-UHFFFAOYSA-O 0.000 description 1
YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
- 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
- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
- A01N43/42—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings condensed with carbocyclic rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/20—Oxygen atoms
- C07D215/24—Oxygen atoms attached in position 8
- C07D215/26—Alcohols; Ethers thereof
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/20—Oxygen atoms
- C07D215/24—Oxygen atoms attached in position 8
- C07D215/26—Alcohols; Ethers thereof
- C07D215/28—Alcohols; Ethers thereof with halogen atoms or nitro radicals in positions 5, 6 or 7
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

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Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Dentistry (AREA)
Environmental Sciences (AREA)
Engineering & Computer Science (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Plant Pathology (AREA)
Toxicology (AREA)
Plural Heterocyclic Compounds (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Quinoline Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Pretreatment Of Seeds And Plants (AREA)

DD83250660A 1982-05-07 1983-05-05 Verfahren zum schuetzen von kulturpflanzen gegen schaedigende wirkungen von agrarchemikalien DD210832A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH284182		1982-05-07

Publications (1)

Publication Number	Publication Date
DD210832A5 true DD210832A5 (de)	1984-06-27

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Application Number	Title	Priority Date	Filing Date
DD83250660A DD210832A5 (de)	1982-05-07	1983-05-05	Verfahren zum schuetzen von kulturpflanzen gegen schaedigende wirkungen von agrarchemikalien

Country Status (26)

Country	Link
US (3)	US4902340A (fr)
EP (1)	EP0094349B1 (fr)
JP (2)	JPS58203967A (fr)
AR (1)	AR241407A1 (fr)
AT (1)	ATE103902T1 (fr)
AU (1)	AU575777B2 (fr)
BG (1)	BG61093B2 (fr)
BR (1)	BR8302394A (fr)
CA (1)	CA1218994A (fr)
CS (1)	CS245782B2 (fr)
DD (1)	DD210832A5 (fr)
DE (1)	DE3382743D1 (fr)
DK (1)	DK173071B1 (fr)
ES (2)	ES522141A0 (fr)
GB (1)	GB2120661B (fr)
GR (1)	GR78348B (fr)
HU (1)	HU190898B (fr)
IL (1)	IL68588A (fr)
KE (1)	KE3870A (fr)
MY (1)	MY8700859A (fr)
NZ (1)	NZ204151A (fr)
PL (1)	PL141315B1 (fr)
RO (1)	RO85265B (fr)
SU (1)	SU1658807A3 (fr)
UA (1)	UA5959A1 (fr)
ZA (1)	ZA833238B (fr)

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EP4230621A1 (fr)	2022-02-22	2023-08-23	Bayer AG	Uraciles d'acide n-benzoïque substitués, ainsi que leurs sels et leur utilisation comme herbicides
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EP4417602A1 (fr)	2023-02-16	2024-08-21	Bayer AG	Pyrazole carboxamides substitués, leurs sels et leur utilisation comme agents herbicides
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AU2024333736A1 (en)	2023-08-30	2026-03-12	Bayer Aktiengesellschaft	Herbicide combinations
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WO2025114250A1 (fr)	2023-11-29	2025-06-05	Bayer Aktiengesellschaft	3-acyl-benzamides et leur utilisation comme herbicides
WO2025132195A1 (fr)	2023-12-19	2025-06-26	Bayer Aktiengesellschaft	Compositions herbicides
WO2025132160A1 (fr)	2023-12-19	2025-06-26	Bayer Aktiengesellschaft	Compositions herbicides
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WO2025132148A1 (fr)	2023-12-21	2025-06-26	Bayer Aktiengesellschaft	Compositions d'adjuvant pour applications agrochimiques
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1983
- 1983-05-02 AT AT83810186T patent/ATE103902T1/de not_active IP Right Cessation
- 1983-05-02 DE DE83810186T patent/DE3382743D1/de not_active Expired - Lifetime
- 1983-05-02 EP EP83810186A patent/EP0094349B1/fr not_active Expired - Lifetime
- 1983-05-03 GB GB08311973A patent/GB2120661B/en not_active Expired
- 1983-05-03 CS CS833107A patent/CS245782B2/cs unknown
- 1983-05-05 IL IL68588A patent/IL68588A/xx not_active IP Right Cessation
- 1983-05-05 DD DD83250660A patent/DD210832A5/de not_active IP Right Cessation
- 1983-05-05 RO RO110868A patent/RO85265B/ro unknown
- 1983-05-05 GR GR71318A patent/GR78348B/el unknown
- 1983-05-05 AR AR83292944A patent/AR241407A1/es active
- 1983-05-06 PL PL1983241841A patent/PL141315B1/pl unknown
- 1983-05-06 ES ES522141A patent/ES522141A0/es active Granted
- 1983-05-06 BR BR8302394A patent/BR8302394A/pt not_active IP Right Cessation
- 1983-05-06 UA UA3592351A patent/UA5959A1/uk unknown
- 1983-05-06 SU SU833592351A patent/SU1658807A3/ru active
- 1983-05-06 HU HU831572A patent/HU190898B/hu unknown
- 1983-05-06 ZA ZA833238A patent/ZA833238B/xx unknown
- 1983-05-06 DK DK198302040A patent/DK173071B1/da active Protection Beyond IP Right Term
- 1983-05-06 NZ NZ204151A patent/NZ204151A/en unknown
- 1983-05-06 CA CA000427668A patent/CA1218994A/fr not_active Expired
- 1983-05-06 AU AU14329/83A patent/AU575777B2/en not_active Expired
- 1983-05-07 JP JP58079991A patent/JPS58203967A/ja active Granted
1984
- 1984-04-12 JP JP59073840A patent/JPH0753642B2/ja not_active Expired - Lifetime
- 1984-09-17 ES ES536425A patent/ES8607244A1/es not_active Expired
1986
- 1986-05-27 US US06/868,372 patent/US4902340A/en not_active Expired - Lifetime
1987
- 1987-12-30 MY MY859/87A patent/MY8700859A/xx unknown
1989
- 1989-03-09 KE KE3870A patent/KE3870A/xx unknown
- 1989-04-14 US US07/338,830 patent/US5023333A/en not_active Expired - Fee Related
1991
- 1991-02-05 US US07/651,119 patent/US5102445A/en not_active Expired - Lifetime
1992
- 1992-06-15 BG BG096474A patent/BG61093B2/bg unknown

Also Published As

Publication number	Publication date
DK173071B1 (da)	1999-12-13
DK204083D0 (da)	1983-05-06
NZ204151A (en)	1986-09-10
CS245782B2 (en)	1986-10-16
GB2120661A (en)	1983-12-07
CA1218994A (fr)	1987-03-10
RO85265A (fr)	1984-09-29
ES8607244A1 (es)	1986-06-01
JPS606603A (ja)	1985-01-14
HU190898B (en)	1986-12-28
US4902340A (en)	1990-02-20
JPS58203967A (ja)	1983-11-28
GB8311973D0 (en)	1983-06-08
JPH0753642B2 (ja)	1995-06-07
RO85265B (ro)	1984-10-30
EP0094349A3 (en)	1985-01-23
BG61093B2 (bg)	1996-10-31
AU1432983A (en)	1983-11-10
IL68588A (en)	1986-12-31
JPH0368862B2 (fr)	1991-10-30
ATE103902T1 (de)	1994-04-15
IL68588A0 (en)	1983-09-30
ES536425A0 (es)	1986-06-01
ES8503212A1 (es)	1985-02-16
GB2120661B (en)	1986-02-12
UA5959A1 (uk)	1994-12-29
AU575777B2 (en)	1988-08-11
DE3382743D1 (de)	1994-05-11
SU1658807A3 (ru)	1991-06-23
EP0094349A2 (fr)	1983-11-16
BR8302394A (pt)	1984-01-10
AR241407A1 (es)	1992-07-31
PL141315B1 (en)	1987-07-31
ES522141A0 (es)	1985-02-16
KE3870A (en)	1989-06-16
PL241841A1 (en)	1985-03-26
MY8700859A (en)	1987-12-31
ZA833238B (en)	1984-02-29
GR78348B (fr)	1984-09-26
EP0094349B1 (fr)	1994-04-06
DK204083A (da)	1983-11-08
US5102445A (en)	1992-04-07
US5023333A (en)	1991-06-11

Legal Events

Date	Code	Title	Description
1996-06-20	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
DD210832A5 (de)	1984-06-27	Verfahren zum schuetzen von kulturpflanzen gegen schaedigende wirkungen von agrarchemikalien
EP0086750B1 (fr)	1987-07-08	Utilisation de dérivés de la quinoléine pour la protection de plantes cultivables
DD202798A5 (de)	1983-10-05	Mittel zum schuetzen von kulturpflanzen vor durch herbizide verursachte phytotoxische schaeden
EP0719261B1 (fr)	2001-12-05	Isoxazolines substituees, leur procede de preparation, agents les contenant et leur utilisation comme reducteurs de phytotoxicite
DE3817192A1 (de)	1989-11-30	1,2,4-triazolderivate enthaltende pflanzenschuetzende mittel sowie neue derivate des 1,2,4-triazols
EP0191736A2 (fr)	1986-08-20	Utilisation de dérivés de la quinoléine pour la protection de plantes cultivables
EP0096657A2 (fr)	1983-12-21	2-Phényl-2-naphtyl- et 2-hétérocyclylpyrimidines comme antidote pour protéger les cultures de plantes avant les dégâts phytotoxiques causés par les herbicides
EP0543878B1 (fr)	1997-01-08	Agents phytosanitaires contenant de l'isoxazoline ou de l'isothiazoline et nouvelles isoxazolines et isothiazolines
EP0378508B1 (fr)	1995-03-01	Antidotes pour modifier la comptabilité des plantes de culture envers les agents agrochimiques
EP0149974B1 (fr)	1988-09-21	Agents pour protéger les plantes cultivées contre l'effet phytotoxique d'herbicides
EP0138773B1 (fr)	1990-08-29	Utilisation de dérivés de la quinoléine pour la protection des plantes cultivables
EP0112289B1 (fr)	1987-09-09	Diesters des acides N-sulfonyl-imino-thiocarboniques comme antagonistes d'herbicides pour protéger les cultures de riz
EP0112280B1 (fr)	1990-08-29	2-Aryl-4,6-dihalogénopyrimidines comme antidote pour protéger les cultures de plantes avant que celles-ci ne subissent des dommages phytotoxiques causés par des herbicides
EP0134198A1 (fr)	1985-03-13	Utilisation des dérivés de quinone pour protéger les plantes cultivées contre l'effet phytotoxique des herbicides
EP0086746B1 (fr)	1986-07-30	Acides phénylamino-oxo-acétiques et leurs esters en tant que anti-dotes d'herbicide pour la protection de plantes cultivées
EP0094351B1 (fr)	1986-07-23	Dérivés de l'acide cyclopropanecarboxylique
EP0126710B1 (fr)	1987-09-30	Moyen pour protéger les plantes cultivées contre l'effet phytotoxique des herbicides
EP0431545A2 (fr)	1991-06-12	Agent herbicide sélectif et agent fongicide
DD231978A5 (de)	1986-01-15	Herbizide zusammensetzung
DD282849A5 (de)	1990-09-26	Mittel zum schuetzen von kulturpflanzen vor der phytotoxischen wirkung von herbiziden
EP0092517B1 (fr)	1986-03-12	Oxime-éthers, leur procédé de préparation, agents contenant ces oxime-éthers et leur usage
CH624554A5 (en)	1981-08-14	Method of protecting crops of plants
DE4011781A1 (de)	1990-10-31	Herbizides mittel
DE3816994A1 (de)	1989-11-30	Herbizide mittel auf der basis von 4-hydroxypyrimidin-derivaten
DE3807532A1 (de)	1989-09-21	Pyrimidin-carbonsaeuren, verfahren zur herstellung und ihre verwendung als herbizide