SK416691A3 - Herbicide compositions - Google Patents
Herbicide compositions Download PDFInfo
- Publication number
- SK416691A3 SK416691A3 SK4166-91A SK416691A SK416691A3 SK 416691 A3 SK416691 A3 SK 416691A3 SK 416691 A SK416691 A SK 416691A SK 416691 A3 SK416691 A3 SK 416691A3
- Authority
- SK
- Slovakia
- Prior art keywords
- formula
- compounds
- weight
- compound
- alkyl
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title claims abstract description 8
- 239000000203 mixture Substances 0.000 title claims description 16
- 230000002363 herbicidal effect Effects 0.000 title claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 5
- 150000001875 compounds Chemical class 0.000 claims description 22
- 239000001257 hydrogen Substances 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 2
- 125000002091 cationic group Chemical group 0.000 claims description 2
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 1
- 230000009429 distress Effects 0.000 claims 1
- 210000001747 pupil Anatomy 0.000 claims 1
- 244000045561 useful plants Species 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 abstract description 3
- 125000000217 alkyl group Chemical group 0.000 abstract description 3
- 150000001768 cations Chemical class 0.000 abstract description 3
- 230000002195 synergetic effect Effects 0.000 abstract description 3
- 239000004480 active ingredient Substances 0.000 description 17
- 230000000694 effects Effects 0.000 description 8
- 101000623895 Bos taurus Mucin-15 Proteins 0.000 description 7
- 239000002253 acid Substances 0.000 description 6
- 238000009472 formulation Methods 0.000 description 6
- 239000008187 granular material Substances 0.000 description 6
- -1 ammonium ions Chemical class 0.000 description 5
- 239000004495 emulsifiable concentrate Substances 0.000 description 5
- 159000000000 sodium salts Chemical class 0.000 description 5
- 241000209082 Lolium Species 0.000 description 4
- 235000005775 Setaria Nutrition 0.000 description 4
- 241000232088 Setaria <nematode> Species 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 235000005781 Avena Nutrition 0.000 description 3
- 241000209761 Avena Species 0.000 description 3
- 241000209504 Poaceae Species 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000003337 fertilizer Substances 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000000080 wetting agent Substances 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 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 235000008515 Setaria glauca Nutrition 0.000 description 2
- 244000010062 Setaria pumila Species 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 239000006185 dispersion 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
- 239000007787 solid Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- JCRNSBKSAQHNIN-UHFFFAOYSA-N 2,4-dibutylnaphthalene-1-sulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(CCCC)=CC(CCCC)=C21 JCRNSBKSAQHNIN-UHFFFAOYSA-N 0.000 description 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
- 241000238876 Acari Species 0.000 description 1
- 244000291564 Allium cepa Species 0.000 description 1
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
- 241000743985 Alopecurus Species 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 235000007320 Avena fatua Nutrition 0.000 description 1
- 241000209764 Avena fatua Species 0.000 description 1
- 235000007558 Avena sp Nutrition 0.000 description 1
- 241000490497 Avena sp. Species 0.000 description 1
- 235000016068 Berberis vulgaris Nutrition 0.000 description 1
- 241000335053 Beta vulgaris Species 0.000 description 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 235000012827 Digitaria sp Nutrition 0.000 description 1
- 241001331845 Equus asinus x caballus Species 0.000 description 1
- 241000283073 Equus caballus Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 244000020551 Helianthus annuus Species 0.000 description 1
- 235000003222 Helianthus annuus Nutrition 0.000 description 1
- 229920001479 Hydroxyethyl methyl cellulose Polymers 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 244000100545 Lolium multiflorum Species 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 244000062793 Sorghum vulgare Species 0.000 description 1
- 235000021536 Sugar beet Nutrition 0.000 description 1
- 101150052863 THY1 gene Proteins 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- YZCKVEUIGOORGS-NJFSPNSNSA-N Tritium Chemical compound [3H] YZCKVEUIGOORGS-NJFSPNSNSA-N 0.000 description 1
- 241000219873 Vicia Species 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- 210000004748 cultured cell Anatomy 0.000 description 1
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexyloxide Natural products O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- QQUPHDGGHUDUKR-UHFFFAOYSA-N dipotassium;oxido-[oxido(oxo)silyl]oxy-oxosilane Chemical compound [K+].[K+].[O-][Si](=O)O[Si]([O-])=O QQUPHDGGHUDUKR-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000000890 drug combination Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 201000004614 iritis Diseases 0.000 description 1
- 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
- 239000004922 lacquer Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003839 salts Chemical class 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
- 239000002904 solvent Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 229910052722 tritium Inorganic materials 0.000 description 1
- 229920002554 vinyl polymer Polymers 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/76—1,3-Oxazoles; Hydrogenated 1,3-oxazoles
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19823240694 DE3240694A1 (de) | 1982-11-04 | 1982-11-04 | Herbizide mittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SK416691A3 true SK416691A3 (en) | 1994-04-06 |
Family
ID=6177263
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK4166-91A SK416691A3 (en) | 1982-11-04 | 1991-12-30 | Herbicide compositions |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US4589908A (cs) |
| EP (1) | EP0110168B1 (cs) |
| AT (1) | ATE22650T1 (cs) |
| AU (1) | AU562458B2 (cs) |
| CA (1) | CA1208926A (cs) |
| CZ (1) | CZ416691A3 (cs) |
| DD (1) | DD212886A5 (cs) |
| DE (2) | DE3240694A1 (cs) |
| SK (1) | SK416691A3 (cs) |
| ZA (1) | ZA838177B (cs) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HU192508B (en) * | 1984-11-19 | 1987-06-29 | Ferenc Tomonicska | Synergic herbicidal compositions comprising 5-(2,4-dichlorphenoxy)-2-nitro-benzoic acid methylester and 2,-/4-(6-chlor-2-benzoxazolyl)-oxy/-phenoxy-propionic acid-ethylester as active substance |
| GB8617741D0 (en) * | 1986-07-21 | 1986-08-28 | May & Baker Ltd | Compositions of matter |
| US5231071A (en) * | 1987-07-10 | 1993-07-27 | Hoechst Aktiengesellschaft | Herbicidial agents |
| DE3917959A1 (de) * | 1989-06-02 | 1990-12-06 | Hoechst Ag | Fluessige herbizide mittel |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2223894C3 (de) * | 1972-05-17 | 1981-07-23 | Hoechst Ag, 6000 Frankfurt | Herbizide Mittel auf Basis von Phenoxycarbonsäurederivaten |
| DE2601548C2 (de) * | 1976-01-16 | 1984-01-26 | Hoechst Ag, 6230 Frankfurt | 2-[4-(2'-Chlor-4'-bromphenoxy)-phenoxy]-propionsäure und Derivate sowie diese enthaltende herbizide Mittel |
| DE2745482A1 (de) * | 1977-10-10 | 1979-04-19 | Hoechst Ag | Herbizides mittel |
| DE2745869A1 (de) * | 1977-10-12 | 1979-04-19 | Hoechst Ag | Herbizide mittel zur bekaempfung von ein- und mehrjaehrigen graesern |
| GB2015341B (en) * | 1978-01-20 | 1982-09-02 | Sumitomo Chemical Co | Selective herbicide composition |
| DE2815287A1 (de) * | 1978-04-08 | 1979-10-18 | Hoechst Ag | Herbizide mittel |
| DE3006439A1 (de) * | 1980-02-21 | 1981-08-27 | Hoechst Ag, 6000 Frankfurt | Herbizide mittel |
| DE3115152A1 (de) * | 1981-04-15 | 1982-12-02 | Hoechst Ag, 6000 Frankfurt | "heterocyclische phenylether und diese enthaltende herbizide mittel" |
-
1982
- 1982-11-04 DE DE19823240694 patent/DE3240694A1/de not_active Withdrawn
-
1983
- 1983-10-29 DE DE8383110859T patent/DE3366652D1/de not_active Expired
- 1983-10-29 AT AT83110859T patent/ATE22650T1/de not_active IP Right Cessation
- 1983-10-29 EP EP83110859A patent/EP0110168B1/de not_active Expired
- 1983-11-02 ZA ZA838177A patent/ZA838177B/xx unknown
- 1983-11-03 DD DD83256311A patent/DD212886A5/de unknown
- 1983-11-03 AU AU20953/83A patent/AU562458B2/en not_active Expired
- 1983-11-03 CA CA000440384A patent/CA1208926A/en not_active Expired
-
1985
- 1985-05-15 US US06/734,756 patent/US4589908A/en not_active Expired - Lifetime
-
1991
- 1991-12-30 SK SK4166-91A patent/SK416691A3/sk unknown
- 1991-12-30 CZ CS914166A patent/CZ416691A3/cs unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DD212886A5 (de) | 1984-08-29 |
| EP0110168A1 (de) | 1984-06-13 |
| US4589908A (en) | 1986-05-20 |
| ATE22650T1 (de) | 1986-10-15 |
| DE3366652D1 (en) | 1986-11-13 |
| ZA838177B (en) | 1984-06-27 |
| AU562458B2 (en) | 1987-06-11 |
| DE3240694A1 (de) | 1984-05-10 |
| CA1208926A (en) | 1986-08-05 |
| EP0110168B1 (de) | 1986-10-08 |
| CZ416691A3 (en) | 1993-01-13 |
| AU2095383A (en) | 1984-05-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| USH750H (en) | Herbicidal suspension concentrate | |
| AU760178B2 (en) | Herbicidally active pyridine sulfonyl urea derivatives | |
| DE1643313A1 (de) | Neue herbicid wirksame Verbindungen und Zusammensetzungen | |
| BG98253A (bg) | Селективно хербицидно средство | |
| JPH05194492A (ja) | 除草剤及び植物成長制御剤としてのピリジルスルホニル尿素化合物の塩類、それらの製造及びそれらの利用方法 | |
| HU198604B (en) | Compositions comprising quinolyloxy derivatives as antidote and ethyl-2-square brackets open 4-(6-chlorobenzoxazolyloxy)-phenoxy square brackets closed -propionate as herbicide | |
| DE69126836T2 (de) | Herbizide | |
| US3253904A (en) | Composition and method for desuckering tobacco | |
| SK416691A3 (en) | Herbicide compositions | |
| PL117199B1 (en) | Herbicide | |
| JP3849040B2 (ja) | 植物保護剤 | |
| UA73598C2 (en) | Herbicide | |
| NO864972L (no) | Plantebeskyttelsesmidler. | |
| US3737298A (en) | 2-fluoro-3-phenyl-2-cyclobutenone as plant auxin | |
| WO1998047356A2 (de) | Dicamba und safener enthaltende herbizide mittel | |
| SU931087A3 (ru) | Способ индуцировани мужской стерильности у растений хлебных злаков и состав дл осуществлени | |
| EP0057367B1 (de) | 2-Pyridyloxyacetanilid-Verbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung | |
| CZ153093A3 (en) | Agent for selective control of weed in cultures of utility plants | |
| US4017297A (en) | Phosphonates for the control of bindweed | |
| WO1998034480A1 (de) | Herbizides mittel | |
| EP0334041A2 (en) | Herbicidal composition | |
| KR900001209B1 (ko) | 설폰 아미드의 제조방법 | |
| EP0544782B1 (en) | A herbicidal composition for paddy field | |
| IE48948B1 (en) | Herbicidal compositions | |
| MXPA04007745A (es) | Composicion herbicida. |