SE446928B - Medel med herbicid verkan innehallande 0-/3-fenyl-6-klorpyridazinyl-(4)/-s-(n-oktyl)-tiokarbonat i blandning med 4-hydroxi-3,5-dijodbensonitril-oktanoat och/eller 4-hydroxi-3,5-dibrombensonitril-oktanoat samt anvendning - Google Patents

Medel med herbicid verkan innehallande 0-/3-fenyl-6-klorpyridazinyl-(4)/-s-(n-oktyl)-tiokarbonat i blandning med 4-hydroxi-3,5-dijodbensonitril-oktanoat och/eller 4-hydroxi-3,5-dibrombensonitril-oktanoat samt anvendning

Info

Publication number: SE446928B
Authority: SE; Sweden
Prior art keywords: octanoate; hydroxy; cch; compound; octyl
Prior art date: 1979-06-22

Application number

SE8004382A

Other languages

English (en)

Swedish (sv)

Other versions

SE8004382L (sv

Inventor

H Leitner

F Raninger

A Diskus

E Auer

Original Assignee

Chemie Linz 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.)

1979-06-22

Filing date

1980-06-12

Publication date

1986-10-20

1980-06-12 Application filed by Chemie Linz Ag filed Critical Chemie Linz Ag

1980-12-23 Publication of SE8004382L publication Critical patent/SE8004382L/xx

1986-10-20 Publication of SE446928B publication Critical patent/SE446928B/sv

Links

239000000203 mixture Substances 0.000 title claims description 21
230000002363 herbicidal effect Effects 0.000 title claims description 14
239000004009 herbicide Substances 0.000 title claims description 8
239000003795 chemical substances by application Substances 0.000 title claims description 5
241000196324 Embryophyta Species 0.000 claims description 34
150000001875 compounds Chemical class 0.000 claims description 21
-1 n-octyl Chemical group 0.000 claims description 10
239000004480 active ingredient Substances 0.000 claims description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
229910052799 carbon Inorganic materials 0.000 claims 1
238000006243 chemical reaction Methods 0.000 claims 1
HVERMFOENITWFA-UHFFFAOYSA-N octoxymethanethioic s-acid Chemical compound CCCCCCCCOC(O)=S HVERMFOENITWFA-UHFFFAOYSA-N 0.000 claims 1
239000013543 active substance Substances 0.000 description 25
DQKWXTIYGWPGOO-UHFFFAOYSA-N (2,6-dibromo-4-cyanophenyl) octanoate Chemical compound CCCCCCCC(=O)OC1=C(Br)C=C(C#N)C=C1Br DQKWXTIYGWPGOO-UHFFFAOYSA-N 0.000 description 8
QBEXFUOWUYCXNI-UHFFFAOYSA-N Ioxynil octanoate Chemical compound CCCCCCCC(=O)OC1=C(I)C=C(C#N)C=C1I QBEXFUOWUYCXNI-UHFFFAOYSA-N 0.000 description 8
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 8
239000003995 emulsifying agent Substances 0.000 description 7
230000002195 synergetic effect Effects 0.000 description 7
239000005606 Pyridate Substances 0.000 description 6
JTZCTMAVMHRNTR-UHFFFAOYSA-N Pyridate Chemical compound CCCCCCCCSC(=O)OC1=CC(Cl)=NN=C1C1=CC=CC=C1 JTZCTMAVMHRNTR-UHFFFAOYSA-N 0.000 description 6
238000002360 preparation method Methods 0.000 description 6
240000005702 Galium aparine Species 0.000 description 5
235000014820 Galium aparine Nutrition 0.000 description 5
230000000996 additive effect Effects 0.000 description 5
HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 4
NVTKOUIRKCHVTG-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile;octanoic acid Chemical compound CCCCCCCC(O)=O.OC1=C(Br)C=C(C#N)C=C1Br NVTKOUIRKCHVTG-UHFFFAOYSA-N 0.000 description 4
241000816457 Galeopsis Species 0.000 description 4
240000002702 Lapsana communis Species 0.000 description 4
235000006761 Lapsana communis Nutrition 0.000 description 4
241001289540 Fallopia convolvulus Species 0.000 description 3
229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
239000012876 carrier material Substances 0.000 description 3
230000018109 developmental process Effects 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
238000000034 method Methods 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000007921 spray Substances 0.000 description 3
244000157790 Buglossoides arvense Species 0.000 description 2
235000004256 Buglossoides arvense Nutrition 0.000 description 2
101100298295 Drosophila melanogaster flfl gene Proteins 0.000 description 2
241001508646 Galeopsis tetrahit Species 0.000 description 2
244000042664 Matricaria chamomilla Species 0.000 description 2
235000007232 Matricaria chamomilla Nutrition 0.000 description 2
240000004674 Papaver rhoeas Species 0.000 description 2
235000007846 Papaver rhoeas Nutrition 0.000 description 2
240000008042 Zea mays Species 0.000 description 2
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 2
235000002017 Zea mays subsp mays Nutrition 0.000 description 2
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
239000000945 filler Substances 0.000 description 2
235000013312 flour Nutrition 0.000 description 2
235000009973 maize Nutrition 0.000 description 2
239000004033 plastic Substances 0.000 description 2
239000000843 powder Substances 0.000 description 2
239000011435 rock Substances 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000000243 solution Substances 0.000 description 2
238000005507 spraying Methods 0.000 description 2
NNJPGOLRFBJNIW-HNNXBMFYSA-N (-)-demecolcine Chemical compound C1=C(OC)C(=O)C=C2[C@@H](NC)CCC3=CC(OC)=C(OC)C(OC)=C3C2=C1 NNJPGOLRFBJNIW-HNNXBMFYSA-N 0.000 description 1
239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 1
UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 description 1
XWSSUYOEOWLFEI-UHFFFAOYSA-N 3-phenylpyridazine Chemical class C1=CC=CC=C1C1=CC=CN=N1 XWSSUYOEOWLFEI-UHFFFAOYSA-N 0.000 description 1
JURYVFBVCAJGBU-UHFFFAOYSA-N 4-hydroxy-3,5-diiodobenzonitrile;octanoic acid Chemical compound CCCCCCCC(O)=O.OC1=C(I)C=C(C#N)C=C1I JURYVFBVCAJGBU-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
240000006122 Chenopodium album Species 0.000 description 1
235000009344 Chenopodium album Nutrition 0.000 description 1
101000888533 Conus ochroleucus Conantokin-Oc Proteins 0.000 description 1
NPOJQCVWMSKXDN-UHFFFAOYSA-N Dacthal Chemical compound COC(=O)C1=C(Cl)C(Cl)=C(C(=O)OC)C(Cl)=C1Cl NPOJQCVWMSKXDN-UHFFFAOYSA-N 0.000 description 1
241001101998 Galium Species 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
239000005574 MCPA Substances 0.000 description 1
108010038016 Mannose-1-phosphate guanylyltransferase Proteins 0.000 description 1
235000017945 Matricaria Nutrition 0.000 description 1
101100348047 Mus musculus Ncam2 gene Proteins 0.000 description 1
235000011096 Papaver Nutrition 0.000 description 1
240000001090 Papaver somniferum Species 0.000 description 1
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
240000006694 Stellaria media Species 0.000 description 1
WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 1
OMOVVBIIQSXZSZ-UHFFFAOYSA-N [6-(4-acetyloxy-5,9a-dimethyl-2,7-dioxo-4,5a,6,9-tetrahydro-3h-pyrano[3,4-b]oxepin-5-yl)-5-formyloxy-3-(furan-3-yl)-3a-methyl-7-methylidene-1a,2,3,4,5,6-hexahydroindeno[1,7a-b]oxiren-4-yl] 2-hydroxy-3-methylpentanoate Chemical compound CC12C(OC(=O)C(O)C(C)CC)C(OC=O)C(C3(C)C(CC(=O)OC4(C)COC(=O)CC43)OC(C)=O)C(=C)C32OC3CC1C=1C=COC=1 OMOVVBIIQSXZSZ-UHFFFAOYSA-N 0.000 description 1
239000000654 additive 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
125000000129 anionic group Chemical group 0.000 description 1
230000008485 antagonism Effects 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
230000006378 damage Effects 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
230000035784 germination Effects 0.000 description 1
239000008187 granular material Substances 0.000 description 1
239000003630 growth substance Substances 0.000 description 1
150000004678 hydrides Chemical class 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 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
229920005610 lignin Polymers 0.000 description 1
239000007788 liquid Substances 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 description 1
125000002347 octyl 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])[H] 0.000 description 1
239000006072 paste Substances 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
QIIPQYDSKRYMFG-UHFFFAOYSA-N phenyl hydrogen carbonate Chemical class OC(=O)OC1=CC=CC=C1 QIIPQYDSKRYMFG-UHFFFAOYSA-N 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
150000004760 silicates 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
239000011780 sodium chloride Substances 0.000 description 1
RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000000080 wetting agent 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
- A01N47/02—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 no bond to a nitrogen atom
- A01N47/06—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 no bond to a nitrogen atom containing —O—CO—O— groups; Thio analogues 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)

SE8004382A 1979-06-22 1980-06-12 Medel med herbicid verkan innehallande 0-/3-fenyl-6-klorpyridazinyl-(4)/-s-(n-oktyl)-tiokarbonat i blandning med 4-hydroxi-3,5-dijodbensonitril-oktanoat och/eller 4-hydroxi-3,5-dibrombensonitril-oktanoat samt anvendning SE446928B (sv)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19792925335 DE2925335A1 (de)	1979-06-22	1979-06-22	Herbizides mittel

Publications (2)

Publication Number	Publication Date
SE8004382L SE8004382L (sv)	1980-12-23
SE446928B true SE446928B (sv)	1986-10-20

Family

ID=6073947

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE8004382A SE446928B (sv)	1979-06-22	1980-06-12	Medel med herbicid verkan innehallande 0-/3-fenyl-6-klorpyridazinyl-(4)/-s-(n-oktyl)-tiokarbonat i blandning med 4-hydroxi-3,5-dijodbensonitril-oktanoat och/eller 4-hydroxi-3,5-dibrombensonitril-oktanoat samt anvendning

Country Status (19)

Country	Link
AR (1)	AR225044A1 (de)
AU (1)	AU526903B2 (de)
BR (1)	BR8003872A (de)
CA (1)	CA1139121A (de)
CS (1)	CS220778B2 (de)
DD (1)	DD151405A1 (de)
DE (1)	DE2925335A1 (de)
DK (1)	DK156982C (de)
FR (1)	FR2459617A1 (de)
GB (1)	GB2051578B (de)
HU (1)	HU185893B (de)
IT (1)	IT1129226B (de)
KE (1)	KE3301A (de)
PL (1)	PL122688B1 (de)
SE (1)	SE446928B (de)
SU (1)	SU934897A3 (de)
TR (1)	TR20588A (de)
UA (1)	UA6316A1 (de)
ZA (1)	ZA803236B (de)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE636416A (de) *	1962-08-30
DE2331398C3 (de) *	1973-06-20	1979-10-11	Lentia Gmbh	Ester von S-PhenyM-hydroxy-e-halogenpyridazinverbindungen, ihre Herstellung und sie enthaltende herbizide Mittel
DE2351553A1 (de) *	1973-10-13	1975-04-24	Basf Ag	Herbizid

1979
- 1979-06-22 DE DE19792925335 patent/DE2925335A1/de not_active Ceased
1980
- 1980-05-29 CA CA000353054A patent/CA1139121A/en not_active Expired
- 1980-05-30 ZA ZA00803236A patent/ZA803236B/xx unknown
- 1980-06-06 DK DK244280A patent/DK156982C/da not_active IP Right Cessation
- 1980-06-11 GB GB8019037A patent/GB2051578B/en not_active Expired
- 1980-06-12 SE SE8004382A patent/SE446928B/sv not_active IP Right Cessation
- 1980-06-16 CS CS435580A patent/CS220778B2/cs unknown
- 1980-06-17 UA UA2936199A patent/UA6316A1/uk unknown
- 1980-06-17 DD DD80221891A patent/DD151405A1/de active Protection Beyond IP Right Term
- 1980-06-17 SU SU802936199A patent/SU934897A3/ru active
- 1980-06-18 AU AU59394/80A patent/AU526903B2/en not_active Ceased
- 1980-06-18 AR AR281438A patent/AR225044A1/es active
- 1980-06-19 FR FR8013600A patent/FR2459617A1/fr active Granted
- 1980-06-20 HU HU801537A patent/HU185893B/hu not_active IP Right Cessation
- 1980-06-20 BR BR8003872A patent/BR8003872A/pt not_active IP Right Cessation
- 1980-06-20 IT IT67972/80A patent/IT1129226B/it active Protection Beyond IP Right Term
- 1980-06-20 PL PL1980225113A patent/PL122688B1/pl unknown
- 1980-06-23 TR TR20588A patent/TR20588A/xx unknown
1983
- 1983-06-27 KE KE3301A patent/KE3301A/xx unknown

Also Published As

Publication number	Publication date
DK156982B (da)	1989-10-30
FR2459617A1 (fr)	1981-01-16
KE3301A (en)	1983-08-05
ZA803236B (en)	1981-05-27
BR8003872A (pt)	1981-01-21
CS220778B2 (en)	1983-04-29
GB2051578A (en)	1981-01-21
CA1139121A (en)	1983-01-11
FR2459617B1 (de)	1982-04-16
AU5939480A (en)	1981-01-08
PL122688B1 (en)	1982-08-31
AU526903B2 (en)	1983-02-03
IT1129226B (it)	1986-06-04
SE8004382L (sv)	1980-12-23
DE2925335A1 (de)	1981-01-08
IT8067972A0 (it)	1980-06-20
DD151405A1 (de)	1981-10-21
TR20588A (tr)	1982-02-01
GB2051578B (en)	1983-06-02
DK244280A (da)	1980-12-23
PL225113A1 (de)	1981-05-22
SU934897A3 (ru)	1982-06-07
UA6316A1 (uk)	1994-12-29
AR225044A1 (es)	1982-02-15
HU185893B (en)	1985-04-28
DK156982C (da)	1990-03-26

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Legal Events

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