DD212642A5 - Herbizide mittel - Google Patents

Herbizide mittel Download PDF

Info

Publication number: DD212642A5
Authority: DD; German Democratic Republic
Prior art keywords: formula; compound; iii; herbicidal; compounds
Prior art date: 1982-11-18

Application number

DD83256757A

Other languages

German (de)

English (en)

Inventor

Hans Schumacher

Rudolf Heinrich

Hans-Guenter Marks

Original Assignee

Hoechst 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.)

1982-11-18

Filing date

1983-11-16

Publication date

1984-08-22

1983-11-16 Application filed by Hoechst Ag filed Critical Hoechst Ag

1984-08-22 Publication of DD212642A5 publication Critical patent/DD212642A5/de

Links

230000002363 herbicidal effect Effects 0.000 title claims abstract description 14
239000004009 herbicide Substances 0.000 title claims description 9
150000001875 compounds Chemical class 0.000 claims abstract description 29
239000000203 mixture Substances 0.000 claims abstract description 20
150000001768 cations Chemical class 0.000 claims abstract description 7
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 7
239000001257 hydrogen Substances 0.000 claims abstract description 4
239000003795 chemical substances by application Substances 0.000 claims abstract description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 3
230000008635 plant growth Effects 0.000 claims abstract description 3
-1 3-chloro-5-trifluoromethyl-pyrid-2-yloxy Chemical group 0.000 claims description 15
241000196324 Embryophyta Species 0.000 claims description 11
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 7
125000000896 monocarboxylic acid group Chemical group 0.000 claims description 3
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 2
AIBQGOMAISTKSR-UHFFFAOYSA-N 6-chloro-1,3-benzothiazole Chemical compound ClC1=CC=C2N=CSC2=C1 AIBQGOMAISTKSR-UHFFFAOYSA-N 0.000 claims 1
238000000034 method Methods 0.000 claims 1
230000000694 effects Effects 0.000 abstract description 10
239000013543 active substance Substances 0.000 description 9
238000009472 formulation Methods 0.000 description 9
239000004480 active ingredient Substances 0.000 description 8
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 8
239000004495 emulsifiable concentrate Substances 0.000 description 8
240000002791 Brassica napus Species 0.000 description 6
239000000843 powder Substances 0.000 description 6
239000000243 solution Substances 0.000 description 6
241001621841 Alopecurus myosuroides Species 0.000 description 5
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
235000011293 Brassica napus Nutrition 0.000 description 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
240000005702 Galium aparine Species 0.000 description 4
235000014820 Galium aparine Nutrition 0.000 description 4
241000209219 Hordeum Species 0.000 description 4
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 4
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
230000000996 additive effect Effects 0.000 description 4
239000003995 emulsifying agent Substances 0.000 description 4
239000008187 granular material Substances 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
229910052708 sodium Inorganic materials 0.000 description 4
239000011734 sodium Substances 0.000 description 4
239000000126 substance Substances 0.000 description 4
230000002195 synergetic effect Effects 0.000 description 4
239000008096 xylene Substances 0.000 description 4
241000499917 Milla Species 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
239000000654 additive Substances 0.000 description 3
239000012141 concentrate Substances 0.000 description 3
244000038559 crop plants Species 0.000 description 3
235000014113 dietary fatty acids Nutrition 0.000 description 3
239000006185 dispersion Substances 0.000 description 3
125000004494 ethyl ester group Chemical group 0.000 description 3
239000000194 fatty acid Substances 0.000 description 3
229930195729 fatty acid Natural products 0.000 description 3
229920000151 polyglycol Polymers 0.000 description 3
239000010695 polyglycol Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000000080 wetting agent Substances 0.000 description 3
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 2
241000743985 Alopecurus Species 0.000 description 2
235000005781 Avena Nutrition 0.000 description 2
241000209761 Avena Species 0.000 description 2
241000209764 Avena fatua Species 0.000 description 2
235000007320 Avena fatua Nutrition 0.000 description 2
235000007558 Avena sp Nutrition 0.000 description 2
241000219198 Brassica Species 0.000 description 2
235000011331 Brassica Nutrition 0.000 description 2
235000006008 Brassica napus var napus Nutrition 0.000 description 2
241001049165 Caria Species 0.000 description 2
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 2
241001101998 Galium Species 0.000 description 2
241000209082 Lolium Species 0.000 description 2
244000042664 Matricaria chamomilla Species 0.000 description 2
235000007232 Matricaria chamomilla Nutrition 0.000 description 2
244000182930 Matricaria sp Species 0.000 description 2
235000008885 Matricaria sp Nutrition 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical class CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
240000006694 Stellaria media Species 0.000 description 2
239000002253 acid Substances 0.000 description 2
125000002877 alkyl aryl group Chemical group 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
239000000969 carrier Substances 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
230000001804 emulsifying effect Effects 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
239000003337 fertilizer 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
239000007788 liquid Substances 0.000 description 2
239000000463 material Substances 0.000 description 2
125000001117 oleyl group Polymers [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 2
229920001522 polyglycol ester Polymers 0.000 description 2
239000007787 solid Substances 0.000 description 2
241000894007 species Species 0.000 description 2
238000003756 stirring Methods 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
238000009736 wetting Methods 0.000 description 2
GXJQMKFJQFGQKV-KHPPLWFESA-N 2-[methyl-[(z)-octadec-9-enoyl]amino]ethanesulfonic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CCS(O)(=O)=O GXJQMKFJQFGQKV-KHPPLWFESA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
101000623895 Bos taurus Mucin-15 Proteins 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
241000490476 Hordeum sp. Species 0.000 description 1
240000005979 Hordeum vulgare Species 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
229920001479 Hydroxyethyl methyl cellulose Polymers 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
241000209510 Liliopsida Species 0.000 description 1
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 1
241000205407 Polygonum Species 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
241000209140 Triticum Species 0.000 description 1
241000209146 Triticum sp. Species 0.000 description 1
YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
230000000274 adsorptive effect Effects 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
230000003042 antagnostic effect Effects 0.000 description 1
HYJSGOXICXYZGS-UHFFFAOYSA-N benazolin Chemical compound C1=CC=C2SC(=O)N(CC(=O)O)C2=C1Cl HYJSGOXICXYZGS-UHFFFAOYSA-N 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
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000000890 drug combination Substances 0.000 description 1
HVCNNTAUBZIYCG-UHFFFAOYSA-N ethyl 2-[4-[(6-chloro-1,3-benzothiazol-2-yl)oxy]phenoxy]propanoate Chemical compound C1=CC(OC(C)C(=O)OCC)=CC=C1OC1=NC2=CC=C(Cl)C=C2S1 HVCNNTAUBZIYCG-UHFFFAOYSA-N 0.000 description 1
239000004744 fabric Substances 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
238000011049 filling Methods 0.000 description 1
238000000227 grinding Methods 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000004615 ingredient Substances 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
235000021374 legumes Nutrition 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical compound OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
239000000047 product Substances 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000004576 sand Substances 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
229920005552 sodium lignosulfonate Polymers 0.000 description 1
KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 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
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles

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)
Medicines Containing Plant Substances (AREA)
Plural Heterocyclic Compounds (AREA)

DD83256757A 1982-11-18 1983-11-16 Herbizide mittel DD212642A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19823242487 DE3242487A1 (de)	1982-11-18	1982-11-18	Herbizide mittel

Publications (1)

Publication Number	Publication Date
DD212642A5 true DD212642A5 (de)	1984-08-22

Family

ID=6178334

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD83256757A DD212642A5 (de)	1982-11-18	1983-11-16	Herbizide mittel

Country Status (9)

Country	Link
EP (1)	EP0110236B1 (da)
AT (1)	ATE24374T1 (da)
CA (1)	CA1208449A (da)
DD (1)	DD212642A5 (da)
DE (2)	DE3242487A1 (da)
DK (1)	DK528183A (da)
FI (1)	FI73119C (da)
PL (1)	PL137072B1 (da)
SU (1)	SU1248529A3 (da)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0210533A1 (en) *	1982-07-13	1987-02-04	Schering Agrochemicals Limited	Herbicidal mixtures

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1518672A (en) *	1974-09-17	1978-07-19	Boots Co Ltd	Herbicidal composition
CA1247625A (en) *	1977-07-22	1988-12-28	Howard Johnston	Trifluoromethyl pyridinyloxyphenoxy propanoic acids and propanols and derivatives thereof and methods of herbicidal use

1982
- 1982-11-18 DE DE19823242487 patent/DE3242487A1/de not_active Withdrawn
1983
- 1983-11-15 EP EP83111429A patent/EP0110236B1/de not_active Expired
- 1983-11-15 DE DE8383111429T patent/DE3368493D1/de not_active Expired
- 1983-11-15 AT AT83111429T patent/ATE24374T1/de not_active IP Right Cessation
- 1983-11-16 FI FI834201A patent/FI73119C/fi not_active IP Right Cessation
- 1983-11-16 DD DD83256757A patent/DD212642A5/de unknown
- 1983-11-16 SU SU833662252A patent/SU1248529A3/ru active
- 1983-11-17 DK DK528183A patent/DK528183A/da not_active Application Discontinuation
- 1983-11-17 CA CA000441424A patent/CA1208449A/en not_active Expired
- 1983-11-17 PL PL1983244612A patent/PL137072B1/pl unknown

Also Published As

Publication number	Publication date
DE3368493D1 (en)	1987-02-05
PL137072B1 (en)	1986-04-30
FI834201L (fi)	1984-05-19
FI73119C (fi)	1987-09-10
DK528183A (da)	1984-05-19
ATE24374T1 (de)	1987-01-15
SU1248529A3 (ru)	1986-07-30
DE3242487A1 (de)	1984-05-24
EP0110236B1 (de)	1986-12-30
PL244612A1 (en)	1984-09-24
CA1208449A (en)	1986-07-29
DK528183D0 (da)	1983-11-17
EP0110236A1 (de)	1984-06-13
FI73119B (fi)	1987-05-29
FI834201A0 (fi)	1983-11-16

Publication	Publication Date	Title
DE69723750T2 (de)	2004-06-03	Herbizide Kombinationen
EP0003805B1 (de)	1982-06-30	Pyridazonverbindungen und diese enthaltende herbizide Zusammensetzungen
DE2839087A1 (de)	1980-03-20	Herbizide mittel
DE69114746T2 (de)	1996-04-18	Herbizide Zusammenschluss enthaltender Aclonifen und mindestens einen substituierten Harnstoff.
DE10127328A1 (de)	2002-12-19	Herbizide Mittel enthaltend Benzoylpyrazole und Safener
DE19728568B4 (de)	2007-06-14	Herbizide Mittel auf Basis von (5-Trifluormethyl-1,3,4-thiadiazol-2-yl-oxy)-essigsäure-N-isopropyl-N-(4fluorphenyl)-amid
DD142643A5 (de)	1980-07-09	Herbizide mittel
CH686210A5 (de)	1996-02-15	Herbizide Zusammensetzung mit einer verminderten Phytotoxizitot.
EP1661459A2 (de)	2006-05-31	Herbizide Mischungen
EP0144796B1 (de)	1989-09-20	Herbizide Mittel
EP0614608B1 (de)	1999-01-07	Synergistische Mischungen zur Bekämpfung von Ackerfuchsschwanz
EP0110236B1 (de)	1986-12-30	Herbizide Mittel
EP0009616B1 (de)	1982-01-27	Herbizides Mittel und Verfahren zur Bekämpfung von Unkräutern
EP0157171B1 (de)	1990-09-19	Herbizide Mittel
EP0110168B1 (de)	1986-10-08	Herbizide Mittel
EP0071973A1 (de)	1983-02-16	Herbizide Mittel
DE19506202A1 (de)	1996-08-29	Herbizide Mittel enthaltend 3-(2-Chlorphenylmethyl)-1-(1-methyl-1-phenylethyl)- und/oder 1-(1-methyl-1-phenylethyl)-3-(4-tolyl)-harnstoffe sowie mindestens ein 3-Phenyluracil
EP0009091B1 (de)	1981-11-18	Verfahren zur selektiven Bekämpfung von unerwünschtem Pflanzenwachstum mit herbiziden Mitteln auf Basis von Acetaniliden und N-Dichloracetyl-2,2-dimethyl-1,3-oxazolidin
DE4428982C1 (de)	1996-05-15	Neue synergistische Herbizide, insbesondere zur Bekämpfung von Ackerfuchsschwanz
EP0208245B1 (de)	1989-04-05	Herbizide und wachstumsregulierende Mittel auf Basis von Chinolinderivaten
DD146238A5 (de)	1981-02-04	Herbizide mittel
DE3434982A1 (de)	1986-04-03	Herbizide mittel
EP0020437B1 (de)	1983-02-23	Halogenacetanilide, ihre Herstellung und diese enthaltende Herbizide
DD204023A5 (de)	1983-11-16	Herbizide mittel
DE3637341A1 (de)	1987-05-07	Herbizide gemische und ihre verwendung zur behandlung von kulturen