CS236881B2 - Synergical herbicide agent - Google Patents

Synergical herbicide agent Download PDF

Info

Publication number: CS236881B2
Authority: CS; Czechoslovakia
Prior art keywords: carbon atoms; compositions; soil; alkyl; cycloalkyl
Prior art date: 1982-05-27

Application number

CS833717A

Other languages

Czech (cs)

English (en)

Inventor

Bareld Egge Groenwold

Original Assignee

Stauffer Chemical Co

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.)

1982-05-27

Filing date

1983-05-26

Publication date

1985-05-15

1983-05-26 Application filed by Stauffer Chemical Co filed Critical Stauffer Chemical Co

1985-05-15 Publication of CS236881B2 publication Critical patent/CS236881B2/cs

Links

239000004009 herbicide Substances 0.000 title abstract description 22
239000000203 mixture Substances 0.000 claims abstract description 54
230000002363 herbicidal effect Effects 0.000 claims abstract description 25
230000002195 synergetic effect Effects 0.000 claims abstract description 15
150000003931 anilides Chemical class 0.000 claims abstract description 8
125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 4
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
239000001257 hydrogen Substances 0.000 claims abstract description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 3
HSGKOMRGFFAUNI-UHFFFAOYSA-N (3-anilino-3-oxopropyl) n-propan-2-ylcarbamate Chemical compound CC(C)NC(=O)OCCC(=O)NC1=CC=CC=C1 HSGKOMRGFFAUNI-UHFFFAOYSA-N 0.000 claims description 2
239000002689 soil Substances 0.000 abstract description 19
150000001875 compounds Chemical class 0.000 abstract description 11
125000000217 alkyl group Chemical group 0.000 abstract description 7
238000011282 treatment Methods 0.000 abstract description 5
229910052757 nitrogen Inorganic materials 0.000 abstract description 4
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 2
125000004432 carbon atom Chemical group C* 0.000 abstract 8
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 2
125000006528 (C2-C6) alkyl group Chemical group 0.000 abstract 1
125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 1
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 abstract 1
125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
125000003342 alkenyl group Chemical group 0.000 abstract 1
244000038559 crop plants Species 0.000 abstract 1
125000000262 haloalkenyl group Chemical group 0.000 abstract 1
125000001188 haloalkyl group Chemical group 0.000 abstract 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
125000005344 pyridylmethyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 abstract 1
239000008187 granular material Substances 0.000 description 17
239000004480 active ingredient Substances 0.000 description 16
241000196324 Embryophyta Species 0.000 description 13
-1 anilide compounds Chemical class 0.000 description 10
239000003995 emulsifying agent Substances 0.000 description 9
239000007788 liquid Substances 0.000 description 9
239000004094 surface-active agent Substances 0.000 description 9
238000012360 testing method Methods 0.000 description 9
239000000969 carrier Substances 0.000 description 8
239000008188 pellet Substances 0.000 description 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
239000000080 wetting agent Substances 0.000 description 8
239000004495 emulsifiable concentrate Substances 0.000 description 7
238000000034 method Methods 0.000 description 7
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
239000002904 solvent Substances 0.000 description 6
239000000126 substance Substances 0.000 description 6
239000013543 active substance Substances 0.000 description 5
239000000729 antidote Substances 0.000 description 5
238000000227 grinding Methods 0.000 description 5
ZTHRQJQJODGZHV-UHFFFAOYSA-N n-phenylpropanamide Chemical class CCC(=O)NC1=CC=CC=C1 ZTHRQJQJODGZHV-UHFFFAOYSA-N 0.000 description 5
239000007787 solid Substances 0.000 description 5
239000011550 stock solution Substances 0.000 description 5
DFCAFRGABIXSDS-UHFFFAOYSA-N Cycloate Chemical compound CCSC(=O)N(CC)C1CCCCC1 DFCAFRGABIXSDS-UHFFFAOYSA-N 0.000 description 4
150000001298 alcohols Chemical class 0.000 description 4
229960000892 attapulgite Drugs 0.000 description 4
235000014113 dietary fatty acids Nutrition 0.000 description 4
239000000194 fatty acid Substances 0.000 description 4
229930195729 fatty acid Natural products 0.000 description 4
239000004615 ingredient Substances 0.000 description 4
239000003621 irrigation water Substances 0.000 description 4
238000002156 mixing Methods 0.000 description 4
229910052625 palygorskite Inorganic materials 0.000 description 4
239000002245 particle Substances 0.000 description 4
238000009331 sowing Methods 0.000 description 4
230000001629 suppression Effects 0.000 description 4
239000005995 Aluminium silicate Substances 0.000 description 3
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-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
239000002253 acid Substances 0.000 description 3
239000000654 additive Substances 0.000 description 3
235000012211 aluminium silicate Nutrition 0.000 description 3
239000011575 calcium Substances 0.000 description 3
229910052791 calcium Inorganic materials 0.000 description 3
239000004927 clay Substances 0.000 description 3
235000021186 dishes Nutrition 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
229910052500 inorganic mineral Inorganic materials 0.000 description 3
238000003973 irrigation Methods 0.000 description 3
230000002262 irrigation Effects 0.000 description 3
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
239000011707 mineral Substances 0.000 description 3
239000002736 nonionic surfactant Substances 0.000 description 3
239000003208 petroleum Substances 0.000 description 3
239000000843 powder Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000011734 sodium Substances 0.000 description 3
239000000243 solution Substances 0.000 description 3
238000005507 spraying Methods 0.000 description 3
150000003467 sulfuric acid derivatives Chemical class 0.000 description 3
235000015112 vegetable and seed oil Nutrition 0.000 description 3
239000008158 vegetable oil Substances 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
244000075850 Avena orientalis Species 0.000 description 2
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 2
239000005909 Kieselgur Substances 0.000 description 2
240000007594 Oryza sativa Species 0.000 description 2
235000007164 Oryza sativa Nutrition 0.000 description 2
239000004721 Polyphenylene oxide Substances 0.000 description 2
230000002745 absorbent Effects 0.000 description 2
239000002250 absorbent Substances 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
125000002877 alkyl aryl group Chemical group 0.000 description 2
125000000129 anionic group Chemical group 0.000 description 2
239000003945 anionic surfactant Substances 0.000 description 2
229940075522 antidotes Drugs 0.000 description 2
239000000440 bentonite Substances 0.000 description 2
229910000278 bentonite Inorganic materials 0.000 description 2
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
238000007796 conventional method Methods 0.000 description 2
239000003085 diluting agent Substances 0.000 description 2
239000000428 dust Substances 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
238000009472 formulation Methods 0.000 description 2
230000035784 germination Effects 0.000 description 2
150000002334 glycols Chemical class 0.000 description 2
230000012010 growth Effects 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
239000000463 material Substances 0.000 description 2
239000012528 membrane Substances 0.000 description 2
239000003094 microcapsule Substances 0.000 description 2
230000000051 modifying effect Effects 0.000 description 2
DEDOPGXGGQYYMW-UHFFFAOYSA-N molinate Chemical compound CCSC(=O)N1CCCCCC1 DEDOPGXGGQYYMW-UHFFFAOYSA-N 0.000 description 2
231100001184 nonphytotoxic Toxicity 0.000 description 2
239000003921 oil Substances 0.000 description 2
235000019198 oils Nutrition 0.000 description 2
230000008635 plant growth Effects 0.000 description 2
229920000570 polyether Polymers 0.000 description 2
229920005989 resin Polymers 0.000 description 2
239000011347 resin Substances 0.000 description 2
235000009566 rice Nutrition 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
235000013311 vegetables Nutrition 0.000 description 2
239000010455 vermiculite Substances 0.000 description 2
229910052902 vermiculite Inorganic materials 0.000 description 2
235000019354 vermiculite Nutrition 0.000 description 2
SLZKCOFZPNAKFW-UHFFFAOYSA-N (3-anilino-3-oxopropyl) N-butylcarbamate Chemical compound CCCCNC(=O)OCCC(=O)NC1=CC=CC=C1 SLZKCOFZPNAKFW-UHFFFAOYSA-N 0.000 description 1
WNFZROKPCJSJPA-UHFFFAOYSA-N (3-anilino-3-oxopropyl) n-(2-methylpropyl)carbamate Chemical compound CC(C)CNC(=O)OCCC(=O)NC1=CC=CC=C1 WNFZROKPCJSJPA-UHFFFAOYSA-N 0.000 description 1
YKCPCWZICZCXON-UHFFFAOYSA-N (3-anilino-3-oxopropyl) n-butan-2-ylcarbamate Chemical compound CCC(C)NC(=O)OCCC(=O)NC1=CC=CC=C1 YKCPCWZICZCXON-UHFFFAOYSA-N 0.000 description 1
OWZPCEFYPSAJFR-UHFFFAOYSA-N 2-(butan-2-yl)-4,6-dinitrophenol Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O OWZPCEFYPSAJFR-UHFFFAOYSA-N 0.000 description 1
235000005781 Avena Nutrition 0.000 description 1
235000021537 Beetroot Nutrition 0.000 description 1
244000056139 Brassica cretica Species 0.000 description 1
235000003351 Brassica cretica Nutrition 0.000 description 1
235000003343 Brassica rupestris Nutrition 0.000 description 1
BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 description 1
NRSGGNJOQQWHGD-UHFFFAOYSA-N C(C)C=1C(=C(SC1)NC(=O)OCCC)CCCC Chemical compound C(C)C=1C(=C(SC1)NC(=O)OCCC)CCCC NRSGGNJOQQWHGD-UHFFFAOYSA-N 0.000 description 1
APRNCHGYBXRIIX-UHFFFAOYSA-N CC[S+]1C(NC([O-])=O)=C(CCC2CCCCC2)C=C1 Chemical compound CC[S+]1C(NC([O-])=O)=C(CCC2CCCCC2)C=C1 APRNCHGYBXRIIX-UHFFFAOYSA-N 0.000 description 1
206010011878 Deafness Diseases 0.000 description 1
YRMLFORXOOIJDR-UHFFFAOYSA-N Dichlormid Chemical compound ClC(Cl)C(=O)N(CC=C)CC=C YRMLFORXOOIJDR-UHFFFAOYSA-N 0.000 description 1
239000001692 EU approved anti-caking agent Substances 0.000 description 1
240000008620 Fagopyrum esculentum Species 0.000 description 1
235000009419 Fagopyrum esculentum Nutrition 0.000 description 1
244000068988 Glycine max Species 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
229920001732 Lignosulfonate Polymers 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
101100400378 Mus musculus Marveld2 gene Proteins 0.000 description 1
244000061176 Nicotiana tabacum Species 0.000 description 1
235000002637 Nicotiana tabacum Nutrition 0.000 description 1
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
241000209504 Poaceae Species 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000002202 Polyethylene glycol Chemical class 0.000 description 1
229920001214 Polysorbate 60 Polymers 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
OKUGPJPKMAEJOE-UHFFFAOYSA-N S-propyl dipropylcarbamothioate Chemical compound CCCSC(=O)N(CCC)CCC OKUGPJPKMAEJOE-UHFFFAOYSA-N 0.000 description 1
244000061458 Solanum melongena Species 0.000 description 1
235000002597 Solanum melongena Nutrition 0.000 description 1
244000300264 Spinacia oleracea Species 0.000 description 1
235000009337 Spinacia oleracea Nutrition 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
235000021536 Sugar beet Nutrition 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
MWTNAQNQXTYLIM-UHFFFAOYSA-N [3-(2,2-dimethylpentanoylamino)phenyl] n-propan-2-ylcarbamate Chemical compound CCCC(C)(C)C(=O)NC1=CC=CC(OC(=O)NC(C)C)=C1 MWTNAQNQXTYLIM-UHFFFAOYSA-N 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
150000003869 acetamides Chemical class 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
238000005054 agglomeration Methods 0.000 description 1
230000002776 aggregation Effects 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
229940051881 anilide analgesics and antipyretics Drugs 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-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
239000001506 calcium phosphate Substances 0.000 description 1
229910000389 calcium phosphate Inorganic materials 0.000 description 1
235000011010 calcium phosphates Nutrition 0.000 description 1
239000002775 capsule Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
230000001427 coherent effect Effects 0.000 description 1
238000011284 combination treatment Methods 0.000 description 1
238000007906 compression Methods 0.000 description 1
230000006835 compression Effects 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000013270 controlled release Methods 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
230000035613 defoliation Effects 0.000 description 1
238000011161 development Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
SPCNPOWOBZQWJK-UHFFFAOYSA-N dimethoxy-(2-propan-2-ylsulfanylethylsulfanyl)-sulfanylidene-$l^{5}-phosphane Chemical class COP(=S)(OC)SCCSC(C)C SPCNPOWOBZQWJK-UHFFFAOYSA-N 0.000 description 1
JMGZBMRVDHKMKB-UHFFFAOYSA-L disodium;2-sulfobutanedioate Chemical class [Na+].[Na+].OS(=O)(=O)C(C([O-])=O)CC([O-])=O JMGZBMRVDHKMKB-UHFFFAOYSA-L 0.000 description 1
238000009826 distribution Methods 0.000 description 1
238000010410 dusting Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000008393 encapsulating agent Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerol Substances OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
208000037824 growth disorder Diseases 0.000 description 1
239000002608 ionic liquid Substances 0.000 description 1
239000002563 ionic surfactant Substances 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
238000002386 leaching Methods 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000000391 magnesium silicate Substances 0.000 description 1
235000012243 magnesium silicates Nutrition 0.000 description 1
239000011159 matrix material Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
239000012764 mineral filler Substances 0.000 description 1
235000010460 mustard Nutrition 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229920003052 natural elastomer Polymers 0.000 description 1
229920001194 natural rubber Polymers 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
150000002917 oxazolidines Chemical class 0.000 description 1
230000035515 penetration Effects 0.000 description 1
231100000208 phytotoxic Toxicity 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
230000008654 plant damage Effects 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920002239 polyacrylonitrile Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920001223 polyethylene glycol Chemical class 0.000 description 1
229920000056 polyoxyethylene ether Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000011148 porous material Substances 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
150000003839 salts Chemical class 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
241000894007 species Species 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000008107 starch Substances 0.000 description 1
230000000638 stimulation Effects 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
229920003051 synthetic elastomer Polymers 0.000 description 1
239000005061 synthetic rubber Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
125000003396 thiol group Chemical group [H]S* 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
239000012991 xanthate Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/22—O-Aryl or S-Aryl esters thereof

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

CS833717A 1982-05-27 1983-05-26 Synergical herbicide agent CS236881B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US38250382A	1982-05-27	1982-05-27

Publications (1)

Publication Number	Publication Date
CS236881B2 true CS236881B2 (en)	1985-05-15

Family

ID=23509243

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS833717A CS236881B2 (en)	1982-05-27	1983-05-26	Synergical herbicide agent

Country Status (14)

Country	Link
EP (1)	EP0095811A3 (de)
JP (1)	JPS58216101A (de)
BG (1)	BG38932A3 (de)
CA (1)	CA1189717A (de)
CS (1)	CS236881B2 (de)
DD (1)	DD209723A5 (de)
DK (1)	DK235783A (de)
FI (1)	FI70774C (de)
GR (1)	GR78572B (de)
HU (1)	HU193040B (de)
IL (1)	IL68792A (de)
PL (1)	PL135734B1 (de)
PT (1)	PT76755B (de)
SU (1)	SU1138004A3 (de)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3836570A (en) *	1968-04-08	1974-09-17	Stauffer Chemical Co	M-amidophenylcarbamates
DE2844806A1 (de) *	1978-10-11	1980-04-24	Schering Ag	Carbanilsaeure- eckige klammer auf 3-(alkylcarbonylamino)-phenyl eckige klammer zu -ester, verfahren zur herstellung dieser verbindungen sowie diese enthaltendes herbizides mittel
ZA8124B (en) *	1980-04-28	1982-01-27	Stauffer Chemical Co	Synergistic herbicidal compostions

1983
- 1983-05-05 FI FI831539A patent/FI70774C/fi not_active IP Right Cessation
- 1983-05-18 GR GR71381A patent/GR78572B/el unknown
- 1983-05-25 JP JP58090862A patent/JPS58216101A/ja active Pending
- 1983-05-25 DK DK235783A patent/DK235783A/da not_active Application Discontinuation
- 1983-05-25 CA CA000428802A patent/CA1189717A/en not_active Expired
- 1983-05-25 PT PT76755A patent/PT76755B/pt unknown
- 1983-05-26 EP EP83200753A patent/EP0095811A3/de not_active Ceased
- 1983-05-26 IL IL68792A patent/IL68792A/xx unknown
- 1983-05-26 HU HU831862A patent/HU193040B/hu unknown
- 1983-05-26 DD DD83251289A patent/DD209723A5/de unknown
- 1983-05-26 CS CS833717A patent/CS236881B2/cs unknown
- 1983-05-26 SU SU833601404A patent/SU1138004A3/ru active
- 1983-05-26 BG BG061092A patent/BG38932A3/xx unknown
- 1983-05-27 PL PL1983242232A patent/PL135734B1/pl unknown

Also Published As

Publication number	Publication date
PT76755B (en)	1986-02-18
PL135734B1 (en)	1985-12-31
FI831539L (fi)	1983-11-28
JPS58216101A (ja)	1983-12-15
BG38932A3 (en)	1986-03-14
HU193040B (en)	1987-08-28
FI70774C (fi)	1986-10-27
PL242232A1 (en)	1984-07-02
CA1189717A (en)	1985-07-02
FI831539A0 (fi)	1983-05-05
DK235783A (da)	1983-11-28
IL68792A (en)	1987-08-31
EP0095811A2 (de)	1983-12-07
SU1138004A3 (ru)	1985-01-30
GR78572B (de)	1984-09-27
DD209723A5 (de)	1984-05-23
EP0095811A3 (de)	1985-04-10
PT76755A (en)	1983-06-01
FI70774B (fi)	1986-07-18
IL68792A0 (en)	1983-09-30
DK235783D0 (da)	1983-05-25

Publication	Publication Date	Title
CA1147158A (en)	1983-05-31	Herbicide compositions of extended soil life
UA75426C2 (en)	2006-04-17	Process of controlling weeds
IT8648593A1 (it)	1988-04-28	Metodo e composizione per aumentare l'attivita' erbicida di sali di n-fosfonometilglicina
CS241084B2 (en)	1986-03-13	Herbicide
US4664699A (en)	1987-05-12	Method of improving residual herbicidal activity and compositions
CS236881B2 (en)	1985-05-15	Synergical herbicide agent
EP0010178B1 (de)	1983-02-16	Herbizide Zusammensetzungen, die ein Thiocarbamat und eine organische Fosfor-Verbindung enthalten, und ihre Verwendung
US4648894A (en)	1987-03-10	Herbicide compositions of extended soil life
US4662930A (en)	1987-05-05	Herbicide compositions of extended soil life
US4629499A (en)	1986-12-16	Herbicide compositions of extended soil life
US4433999A (en)	1984-02-28	Herbicide compositions containing soil life extenders and antidotes
US4652302A (en)	1987-03-24	Herbicide compositions of extended soil life
EP0100909B1 (de)	1986-06-04	Herbizide Zusammensetzungen mit längerer Lebensdauer im Boden
US4762548A (en)	1988-08-09	Herbicide compositions of extended soil life
US4652298A (en)	1987-03-24	Herbicide compositions of extended soil life
US4422869A (en)	1983-12-27	Halogenated allylthioisopropyl N-methylcarbamates as herbicide extenders
US4652296A (en)	1987-03-24	Herbicide compositions of extended soil life
US4652300A (en)	1987-03-24	Herbicide compositions of extended soil life
US4613358A (en)	1986-09-23	Herbicide compositions of extended soil life
US4381936A (en)	1983-05-03	Herbicide compositions of extended soil life
US4386955A (en)	1983-06-07	O-(Substituted phenyl) N-methylcarbamates as herbicide extenders
US4652301A (en)	1987-03-24	Herbicide compositions of extended soil life
US4546199A (en)	1985-10-08	Halogenated allylthioisopropyl N-methyl carbamates as herbicide extenders
CS241085B2 (en)	1986-03-13	Herbicide
CS241126B2 (cs)	1986-03-13	Herbicidnf prostředek s prodlouženou stálosti v půdě