LU84296A1 - Composes herbicides derives d'acides phenoxybenzoiques - Google Patents

Composes herbicides derives d'acides phenoxybenzoiques Download PDF

Info

Publication number: LU84296A1
Authority: LU; Luxembourg
Prior art keywords: οοοο; compounds; active ingredient; active material; sodium
Prior art date: 1981-07-27

Application number

LU84296A

Other languages

English (en)

French (fr)

Inventor

James J Steffens

El-Ahmadi I Heiba

Original Assignee

Rhone Poulenc Agrochimie

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.)

1981-07-27

Filing date

1982-07-26

Publication date

1984-03-22

1981-07-27 Priority claimed from US06/286,935 external-priority patent/US4744818A/en

1982-07-26 Application filed by Rhone Poulenc Agrochimie filed Critical Rhone Poulenc Agrochimie

1984-03-22 Publication of LU84296A1 publication Critical patent/LU84296A1/fr

Links

150000001875 compounds Chemical class 0.000 title description 30
239000004009 herbicide Substances 0.000 title description 9
230000002363 herbicidal effect Effects 0.000 title description 7
239000002253 acid Substances 0.000 title description 4
150000007513 acids Chemical class 0.000 title 1
235000000509 Chenopodium ambrosioides Nutrition 0.000 claims description 2
244000098897 Chenopodium botrys Species 0.000 claims description 2
235000005490 Chenopodium botrys Nutrition 0.000 claims description 2
235000007516 Chrysanthemum Nutrition 0.000 claims 1
240000005250 Chrysanthemum indicum Species 0.000 claims 1
241000234653 Cyperus Species 0.000 claims 1
239000000203 mixture Substances 0.000 description 37
241000196324 Embryophyta Species 0.000 description 27
239000004480 active ingredient Substances 0.000 description 23
239000011149 active material Substances 0.000 description 23
239000000843 powder Substances 0.000 description 17
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 11
239000002689 soil Substances 0.000 description 11
239000007921 spray Substances 0.000 description 11
238000011282 treatment Methods 0.000 description 11
239000004094 surface-active agent Substances 0.000 description 10
239000000460 chlorine Substances 0.000 description 9
230000006378 damage Effects 0.000 description 9
-1 hydrocarbon radical Chemical group 0.000 description 9
239000007788 liquid Substances 0.000 description 9
125000000217 alkyl group Chemical group 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 8
239000008187 granular material Substances 0.000 description 8
239000007787 solid Substances 0.000 description 8
235000010469 Glycine max Nutrition 0.000 description 7
238000000034 method Methods 0.000 description 7
229910052708 sodium Inorganic materials 0.000 description 7
239000011734 sodium Substances 0.000 description 7
239000000243 solution Substances 0.000 description 7
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
244000068988 Glycine max Species 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
125000004432 carbon atom Chemical group C* 0.000 description 6
239000004495 emulsifiable concentrate Substances 0.000 description 6
239000000839 emulsion Substances 0.000 description 6
239000000377 silicon dioxide Substances 0.000 description 6
238000005507 spraying Methods 0.000 description 6
239000000725 suspension Substances 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 5
239000000654 additive Substances 0.000 description 5
235000013339 cereals Nutrition 0.000 description 5
239000003795 chemical substances by application Substances 0.000 description 5
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 5
125000005843 halogen group Chemical group 0.000 description 5
239000003381 stabilizer Substances 0.000 description 5
239000005995 Aluminium silicate Substances 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
239000000853 adhesive Substances 0.000 description 4
230000001070 adhesive effect Effects 0.000 description 4
235000012211 aluminium silicate Nutrition 0.000 description 4
229910052801 chlorine Inorganic materials 0.000 description 4
239000000470 constituent Substances 0.000 description 4
238000002844 melting Methods 0.000 description 4
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239000000047 product Substances 0.000 description 4
150000003254 radicals Chemical class 0.000 description 4
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 4
239000004563 wettable powder Substances 0.000 description 4
PKRSYEPBQPFNRB-UHFFFAOYSA-N 2-phenoxybenzoic acid Chemical class OC(=O)C1=CC=CC=C1OC1=CC=CC=C1 PKRSYEPBQPFNRB-UHFFFAOYSA-N 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
229920000742 Cotton Polymers 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
229910019142 PO4 Inorganic materials 0.000 description 3
241001506766 Xanthium Species 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
150000001298 alcohols Chemical class 0.000 description 3
235000005822 corn Nutrition 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
239000000945 filler Substances 0.000 description 3
238000009472 formulation Methods 0.000 description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
238000010348 incorporation Methods 0.000 description 3
230000000149 penetrating effect Effects 0.000 description 3
239000003208 petroleum Substances 0.000 description 3
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
239000010452 phosphate Substances 0.000 description 3
235000021317 phosphate Nutrition 0.000 description 3
239000002002 slurry Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
241000894007 species Species 0.000 description 3
239000000126 substance Substances 0.000 description 3
ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 3
229960000278 theophylline Drugs 0.000 description 3
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 3
239000000080 wetting agent Substances 0.000 description 3
239000008096 xylene Substances 0.000 description 3
TVFWYUWNQVRQRG-UHFFFAOYSA-N 2,3,4-tris(2-phenylethenyl)phenol Polymers C=1C=CC=CC=1C=CC1=C(C=CC=2C=CC=CC=2)C(O)=CC=C1C=CC1=CC=CC=C1 TVFWYUWNQVRQRG-UHFFFAOYSA-N 0.000 description 2
XLLIQLLCWZCATF-UHFFFAOYSA-N 2-methoxyethyl acetate Chemical compound COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 2
241000219144 Abutilon Species 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
240000008100 Brassica rapa Species 0.000 description 2
235000011292 Brassica rapa Nutrition 0.000 description 2
235000004977 Brassica sinapistrum Nutrition 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
241000219146 Gossypium Species 0.000 description 2
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 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
239000005708 Sodium hypochlorite Substances 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
125000005599 alkyl carboxylate group Chemical group 0.000 description 2
150000005840 aryl radicals Chemical group 0.000 description 2
239000011230 binding agent Substances 0.000 description 2
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
239000000969 carrier Substances 0.000 description 2
239000003153 chemical reaction reagent Substances 0.000 description 2
230000007797 corrosion Effects 0.000 description 2
238000005260 corrosion Methods 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
238000010790 dilution Methods 0.000 description 2
239000012895 dilution Substances 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
238000001035 drying Methods 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
239000003337 fertilizer Substances 0.000 description 2
238000005469 granulation Methods 0.000 description 2
230000003179 granulation Effects 0.000 description 2
238000000227 grinding Methods 0.000 description 2
WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 2
238000005470 impregnation Methods 0.000 description 2
239000003112 inhibitor Substances 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
239000003621 irrigation water Substances 0.000 description 2
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
238000005259 measurement Methods 0.000 description 2
239000011707 mineral Substances 0.000 description 2
DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
125000004433 nitrogen atom Chemical group N* 0.000 description 2
239000003921 oil Substances 0.000 description 2
FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
150000002989 phenols Chemical class 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
230000008635 plant growth Effects 0.000 description 2
125000006684 polyhaloalkyl group Polymers 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
239000002243 precursor Substances 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
238000007873 sieving Methods 0.000 description 2
SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 2
229920005552 sodium lignosulfonate Polymers 0.000 description 2
239000008247 solid mixture Substances 0.000 description 2
238000009331 sowing Methods 0.000 description 2
238000003756 stirring Methods 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
125000004001 thioalkyl group Chemical group 0.000 description 2
239000013008 thixotropic agent Substances 0.000 description 2
WHOZNOZYMBRCBL-OUKQBFOZSA-N (2E)-2-Tetradecenal Chemical compound CCCCCCCCCCC\C=C\C=O WHOZNOZYMBRCBL-OUKQBFOZSA-N 0.000 description 1
UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical class COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 1
240000001592 Amaranthus caudatus Species 0.000 description 1
235000009328 Amaranthus caudatus Nutrition 0.000 description 1
244000105624 Arachis hypogaea Species 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
240000006122 Chenopodium album Species 0.000 description 1
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239000001692 EU approved anti-caking agent Substances 0.000 description 1
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NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
238000005481 NMR spectroscopy Methods 0.000 description 1
229910000503 Na-aluminosilicate Inorganic materials 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
231100000674 Phytotoxicity Toxicity 0.000 description 1
241000209504 Poaceae Species 0.000 description 1
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240000003461 Setaria viridis Species 0.000 description 1
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235000010086 Setaria viridis var. viridis Nutrition 0.000 description 1
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229920002125 Sokalan® Polymers 0.000 description 1
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ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
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229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical group 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
150000004996 alkyl benzenes Chemical class 0.000 description 1
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150000001412 amines Chemical class 0.000 description 1
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150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
239000003849 aromatic solvent Substances 0.000 description 1
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125000004429 atom Chemical group 0.000 description 1
229940077388 benzenesulfonate Drugs 0.000 description 1
239000007844 bleaching agent Substances 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
125000001246 bromo group Chemical group Br* 0.000 description 1
239000011575 calcium Substances 0.000 description 1
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235000019993 champagne Nutrition 0.000 description 1
150000001805 chlorine compounds Chemical class 0.000 description 1
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125000004093 cyano group Chemical group *C#N 0.000 description 1
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238000010586 diagram Methods 0.000 description 1
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235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
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239000008202 granule composition Substances 0.000 description 1
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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 1
239000000463 material Substances 0.000 description 1
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239000003607 modifier Substances 0.000 description 1
125000000896 monocarboxylic acid group Chemical group 0.000 description 1
125000000018 nitroso group Chemical group N(=O)* 0.000 description 1
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235000002252 panizo Nutrition 0.000 description 1
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239000008389 polyethoxylated castor oil Substances 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
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229920001282 polysaccharide Polymers 0.000 description 1
239000005017 polysaccharide Substances 0.000 description 1
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238000002360 preparation method Methods 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
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102220254284 rs755928199 Human genes 0.000 description 1
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150000004760 silicates Chemical class 0.000 description 1
239000000429 sodium aluminium silicate Substances 0.000 description 1
235000012217 sodium aluminium silicate Nutrition 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
HIEHAIZHJZLEPQ-UHFFFAOYSA-M sodium;naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 HIEHAIZHJZLEPQ-UHFFFAOYSA-M 0.000 description 1
239000004550 soluble concentrate Substances 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
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XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
238000012360 testing method Methods 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
239000003021 water soluble solvent Substances 0.000 description 1
239000001993 wax Substances 0.000 description 1
238000009333 weeding Methods 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/58—1,2-Diazines; Hydrogenated 1,2-diazines
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/36—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
- C07C303/40—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reactions not involving the formation of sulfonamide groups
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
- A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
- A01N41/04—Sulfonic acids; Derivatives thereof
- A01N41/06—Sulfonic acid amides
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- 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
- 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
- A01N51/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring

Landscapes

Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Wood Science & Technology (AREA)
Environmental Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Zoology (AREA)
Dentistry (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

LU84296A 1981-07-27 1982-07-26 Composes herbicides derives d'acides phenoxybenzoiques LU84296A1 (fr)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
US28699881A	1981-07-27	1981-07-27
US28699881		1981-07-27
US28693581		1981-07-27
US06/286,935 US4744818A (en)	1981-07-27	1981-07-27	Herbicidal N-halo-5(substituted-phenoxy or -pyridyloxy)-2-substituted benzoic acid sulfonamides and sulfamates

Publications (1)

Publication Number	Publication Date
LU84296A1 true LU84296A1 (fr)	1984-03-22

Family

ID=26964152

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LU84296A LU84296A1 (fr)	1981-07-27	1982-07-26	Composes herbicides derives d'acides phenoxybenzoiques

Country Status (21)

Country	Link
KR (1)	KR840000480A (de)
AU (1)	AU8642882A (de)
BR (1)	BR8204350A (de)
DD (1)	DD203679A5 (de)
DE (1)	DE3227818A1 (de)
DK (1)	DK333382A (de)
ES (1)	ES8305715A1 (de)
FR (1)	FR2510103A1 (de)
GB (1)	GB2103609A (de)
GR (1)	GR76231B (de)
IL (1)	IL66241A0 (de)
IT (1)	IT1198401B (de)
LU (1)	LU84296A1 (de)
MA (1)	MA19550A1 (de)
NL (1)	NL8202993A (de)
OA (1)	OA07161A (de)
PL (1)	PL132197B1 (de)
PT (1)	PT75320B (de)
SE (1)	SE8204457L (de)
SU (1)	SU1149857A3 (de)
TR (1)	TR21427A (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
TW201101999A (en) *	2009-06-12	2011-01-16	United Phosphorus Ltd	Herbicidal composition

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0003416B1 (de) *	1978-01-19	1981-08-26	Imperial Chemical Industries Plc	Diphenylätherverbindungen, Verfahren zu ihrer Anwendung, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Herbizide

1982
- 1982-06-25 FR FR8211330A patent/FR2510103A1/fr active Granted
- 1982-07-06 IL IL66241A patent/IL66241A0/xx unknown
- 1982-07-21 MA MA19758A patent/MA19550A1/fr unknown
- 1982-07-23 IT IT22549/82A patent/IT1198401B/it active
- 1982-07-23 PL PL1982237636A patent/PL132197B1/pl unknown
- 1982-07-26 DE DE19823227818 patent/DE3227818A1/de not_active Withdrawn
- 1982-07-26 ES ES514355A patent/ES8305715A1/es not_active Expired
- 1982-07-26 AU AU86428/82A patent/AU8642882A/en not_active Abandoned
- 1982-07-26 OA OA57753A patent/OA07161A/xx unknown
- 1982-07-26 NL NL8202993A patent/NL8202993A/nl not_active Application Discontinuation
- 1982-07-26 LU LU84296A patent/LU84296A1/fr unknown
- 1982-07-26 SU SU823467050A patent/SU1149857A3/ru active
- 1982-07-26 GR GR68860A patent/GR76231B/el unknown
- 1982-07-26 DK DK333382A patent/DK333382A/da not_active Application Discontinuation
- 1982-07-26 PT PT75320A patent/PT75320B/pt unknown
- 1982-07-26 BR BR8204350A patent/BR8204350A/pt unknown
- 1982-07-26 SE SE8204457A patent/SE8204457L/ not_active Application Discontinuation
- 1982-07-26 GB GB08221570A patent/GB2103609A/en not_active Withdrawn
- 1982-07-27 TR TR21427A patent/TR21427A/xx unknown
- 1982-07-27 KR KR1019820003346A patent/KR840000480A/ko not_active Withdrawn
- 1982-07-27 DD DD82241977A patent/DD203679A5/de unknown

Also Published As

Publication number	Publication date
ES514355A0 (es)	1983-04-16
ES8305715A1 (es)	1983-04-16
SE8204457D0 (sv)	1982-07-26
SE8204457L (sv)	1983-01-28
FR2510103A1 (fr)	1983-01-28
DK333382A (da)	1983-01-28
GB2103609A (en)	1983-02-23
KR840000480A (ko)	1984-02-22
SU1149857A3 (ru)	1985-04-07
IT8222549A0 (it)	1982-07-23
PL132197B1 (en)	1985-02-28
IL66241A0 (en)	1982-11-30
DD203679A5 (de)	1983-11-02
TR21427A (tr)	1984-06-01
IT8222549A1 (it)	1984-01-23
OA07161A (fr)	1984-03-31
PL237636A1 (en)	1983-09-12
PT75320B (fr)	1985-11-29
BR8204350A (pt)	1983-07-19
PT75320A (fr)	1982-08-01
FR2510103B1 (de)	1984-06-29
IT1198401B (it)	1988-12-21
MA19550A1 (fr)	1983-04-01
GR76231B (de)	1984-08-04
DE3227818A1 (de)	1983-02-24
AU8642882A (en)	1983-02-03
NL8202993A (nl)	1983-02-16

Publication	Publication Date	Title
EP0192583B1 (de)	1989-05-24	Auf einer Verbindung der N-(Phosphonomethylglycyl)-sulfonylamin-Art basierende herbizide Mischungen
CH629487A5 (en)	1982-04-30	4-(5-Fluoromethyl-2-pyridyloxy)phenoxyalkanecarboxylic acids, derivatives of these and herbicidal compositions containing them
FR3119622A1 (fr)	2022-08-12	Nouvelle forme cristalline de pyroxasulfone, procédés de préparation et utilisation de celle-ci
EP0135454B1 (de)	1989-05-31	Herbizide des Sulfonimid-Typs mit Aminomethyl Phosphon-Gruppe
KR910001130B1 (ko)	1991-02-25	벤조트리아졸의 제조방법
CH638787A5 (fr)	1983-10-14	Esters d'acides 4-(4-(5-trifluoromethyl-2-pyridyloxy)-phenoxy)-2-pentenoiques utiles comme herbicides.
CH623987A5 (de)	1981-07-15
FR2586416A1 (fr)	1987-02-27	Nouvelles 2-(1-(3-chlorallyloxyamino)alkylidene)-5-alkylthioalkyl-cyclohexane-1,3-diones, composition herbicide les contenant, leur procede de preparation et leurs applications
EP0189358B1 (de)	1988-09-28	N-(Phosphonomethylglycyl)-Sulfonylamine-ähnliche Herbizide
EP0112262A1 (de)	1984-06-27	Benzylcarbamoylpyridin-Derivate
FR2594437A1 (fr)	1987-08-21	Nouveaux derives du cyano-2 benzimidazole, leur preparation, les compositions les contenant et leur utilisation comme fongicide
EP0034556B1 (de)	1984-02-01	Das Pflanzenwachstum regulierende Zusammensetzungen, die als aktive Substanz Derivate von 2-Methylen-succinamidsäure enthalten, und Derivate dieser Säure, die in diesen Zusammensetzungen verwendbar sind
LU84301A1 (fr)	1984-03-22	Composes herbicides derives d'acides phenoxybenzoiques et leurs procedes de preparation et d'utilisation
LU84298A1 (fr)	1984-03-22	Composes herbicides derives d'acides phenoxybenzoiques
EP0340216B1 (de)	1993-05-19	Unkrautvertilgende zubereitungen vom glyphosattyp und vom phenoxybenzoesäuretyp
BE893941A (fr)	1983-01-26	Composes herbicides derives d'acides phenoxybenzoiques
EP0249567A2 (de)	1987-12-16	Propargyloxybenzolderivate, ihre Herstellung und sie enthaltende fungizide Zusammensetzungen
EP0091387A2 (de)	1983-10-12	Sulfonimidgruppe enthaltende Phenoxybenzoesäurederivate mit herbizider Wirkung
FR2510103A1 (fr)	1983-01-28	Composes herbicides derives d'acides phenoxybenzoiques
BE834495A (fr)	1976-02-02	Compose herbicide, composition herbicide contenant et leur procede d'utilisation
EP0483027A2 (de)	1992-04-29	Triazolpyridazine, Verfahren zu ihrer Herstellung ihre Verwendung als Herbizide und ihre Zwischenprodukte
EP0016132A1 (de)	1980-10-01	Neues substituiertes phenylharnstoff-herbizid
FR2525593A1 (fr)	1983-10-28	Derives d'acides phenoxybenzoiques, leur preparation et leur utilisation pour le desherbage des cultures
LU84116A1 (fr)	1984-03-02	Derives d'acides phenoxybenzoiques,leur preparation et leur utilisation pour le desherbage des cultures
FR2589327A1 (fr)	1987-05-07	Melanges herbicides de derives d'acides pyridinoxyalcanoiques et de derives d'acides phenoxybenzoiques et leur utilisation pour le traitement des cultures