AP351A - Mixed agrochemical combination. - Google Patents
Mixed agrochemical combination. Download PDFInfo
- Publication number
- AP351A AP351A APAP/P/1992/000455A AP9200455A AP351A AP 351 A AP351 A AP 351A AP 9200455 A AP9200455 A AP 9200455A AP 351 A AP351 A AP 351A
- Authority
- AP
- ARIPO
- Prior art keywords
- plant
- combination
- process according
- active materials
- fungicide
- Prior art date
Links
- 239000003905 agrochemical Substances 0.000 title claims abstract description 8
- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000005906 Imidacloprid Substances 0.000 claims abstract description 12
- 239000000417 fungicide Substances 0.000 claims abstract description 12
- 229940056881 imidacloprid Drugs 0.000 claims abstract description 12
- 230000000855 fungicidal effect Effects 0.000 claims abstract description 11
- 201000010099 disease Diseases 0.000 claims abstract description 10
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 10
- 241000238631 Hexapoda Species 0.000 claims abstract description 9
- 125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims abstract description 8
- 239000002917 insecticide Substances 0.000 claims abstract description 7
- 239000011149 active material Substances 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 12
- PPDBOQMNKNNODG-NTEUORMPSA-N (5E)-5-(4-chlorobenzylidene)-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentanol Chemical group C1=NC=NN1CC1(O)C(C)(C)CC\C1=C/C1=CC=C(Cl)C=C1 PPDBOQMNKNNODG-NTEUORMPSA-N 0.000 claims description 9
- 239000005859 Triticonazole Substances 0.000 claims description 9
- 239000004094 surface-active agent Substances 0.000 claims description 9
- 239000002689 soil Substances 0.000 claims description 4
- 239000012872 agrochemical composition Substances 0.000 claims 2
- 235000013339 cereals Nutrition 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 35
- 239000000843 powder Substances 0.000 description 18
- 241000196324 Embryophyta Species 0.000 description 16
- 239000000470 constituent Substances 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- 239000005995 Aluminium silicate Substances 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 235000012211 aluminium silicate Nutrition 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 241001600407 Aphis <genus> Species 0.000 description 5
- 239000004495 emulsifiable concentrate Substances 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 241001123569 Puccinia recondita Species 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- 235000019993 champagne Nutrition 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 230000035515 penetration Effects 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- 239000000080 wetting agent Substances 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 238000010410 dusting Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 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 3
- 230000008635 plant growth Effects 0.000 description 3
- 229920000151 polyglycol Polymers 0.000 description 3
- 239000010695 polyglycol Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 241000233866 Fungi Species 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- 206010061217 Infestation Diseases 0.000 description 2
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 241000209140 Triticum Species 0.000 description 2
- 235000021307 Triticum Nutrition 0.000 description 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N Vilsmeier-Haack reagent Natural products CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- 229920005551 calcium lignosulfonate Polymers 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 230000000749 insecticidal effect Effects 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
- 239000011368 organic material Substances 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000004550 soluble concentrate Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 239000004546 suspension concentrate Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 239000013008 thixotropic agent Substances 0.000 description 2
- 239000004563 wettable powder Substances 0.000 description 2
- TVFWYUWNQVRQRG-UHFFFAOYSA-N 2,3,4-tris(2-phenylethenyl)phenol Chemical class 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 1
- UQFGXXUMKQOQPH-UHFFFAOYSA-N 2-[(4-chlorophenyl)methylidene]-1-(1,2,4-triazol-1-ylmethyl)cyclohexan-1-ol Chemical compound C1CCCC(=CC=2C=CC(Cl)=CC=2)C1(O)CN1C=NC=N1 UQFGXXUMKQOQPH-UHFFFAOYSA-N 0.000 description 1
- IULJSGIJJZZUMF-UHFFFAOYSA-N 2-hydroxybenzenesulfonic acid Chemical compound OC1=CC=CC=C1S(O)(=O)=O IULJSGIJJZZUMF-UHFFFAOYSA-N 0.000 description 1
- PPDBOQMNKNNODG-UHFFFAOYSA-N 5-[(4-chlorophenyl)methylidene]-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentan-1-ol Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1=CC1=CC=C(Cl)C=C1 PPDBOQMNKNNODG-UHFFFAOYSA-N 0.000 description 1
- 239000001692 EU approved anti-caking agent Substances 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 208000031888 Mycoses Diseases 0.000 description 1
- 229910000503 Na-aluminosilicate Inorganic materials 0.000 description 1
- 231100000674 Phytotoxicity Toxicity 0.000 description 1
- 206010037888 Rash pustular Diseases 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000002528 anti-freeze Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexyloxide Natural products O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000006185 dispersion Substances 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
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 230000003993 interaction Effects 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
- 150000002576 ketones Chemical class 0.000 description 1
- 239000008268 mayonnaise Substances 0.000 description 1
- 235000010746 mayonnaise Nutrition 0.000 description 1
- 239000004531 microgranule Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 125000000913 palmityl 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])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003415 peat Substances 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- -1 poly(acrylic acids) Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 208000029561 pustule Diseases 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 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
- 229920005552 sodium lignosulfonate Polymers 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical group [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 230000001018 virulence Effects 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000008096 xylene 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
-
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- 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)
- 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)
Abstract
Agrochemical combination.IT comprises an effective quantity of a benzylidene azolylmethylcycloalkane fungicide and an effective quantity of the insecticide imidacloprid.APplicable to the protection of plants against diseases and insects
Description
Mixed agrochemical combination
The present invention relates to new agrochemical combinations for the protection of plants comprising both an active fungicidal material and an active insecticidal material as well as a process for the treatment of plants using these combinations.
In this specification, including the accompanying claims it is to be understood that the term plant'’ embraces an entire plant, a part of a plant or plant propagation material, especially a seed.
More particularly, the subject of the invention is an agrochemical combination for the protection of plants against diseases and plant-eating insects, characterised in that it comprises at least an effective quantity of a benzylidene azolylmethylcycloalkane fungicide and at least an effective quantity of the insecticide imidacloprid.
There may be cited, as the benzylidene azolylmethylcycloalkane fungicide, in particular those described in the European Patent Application 0,378,953, and preferably 2-(4-chlorobenzylidene)-5,5-dimethyl-l-(1H-1,2,4triazol-l-ylmethyl)-1-cyclopentanol or triticonazole and 2-(4chlorobenzylidene)-1-(1H-1,2,4-triazol-l-ylmethyl)-1cyclohexanol.
Imidacloprid is the common name for l-(6-chloro-3pyridylmethyl)-N-nitroimidazolidin-2-ylidene-amine described for its insecticidal properties, especially in the proceedings Pests and Diseases, Brighton Crop Protection Conference,
1990, p. 21.
It has been found that combinations based on these two types of products are particularly advantageous for the protection of plants against diseases and plant-eating insects.
The combinations according to the invention can be preferably used for the protection of seeds or in soil treatment.
The fungicide is preferably used at a dose of from
2.5 to 250 g per quintal and the insecticide is preferably used at a dose of from 25 to 2000 g per quintal of seed.
A further subject of the invention is compositions based on each of the two active materials.
The invention additionally comprises a process for the treatment of plants for the protection of plants against diseases and plant-eating insects, characterised in that a combination of the two active materials is applied either simultaneously or successively so as to have the conjugate effect.
The following examples are given in order to illustrate the combinations, compositions and treatment according to the invention.
EXAMPLE
Wheat seeds of the Talent variety were treated with:
- on the one hand, triticonazole alone, at doses of 60, 120 and 180 g of active material per quintal (a.m.g./q),
- on the other hand, imidacloprid alone, at doses of 200 and 400 g (a.m.g./q),
- finally, triticonazole + imidacloprid mixtures, each active material being individually at each of the doses indicated above.
An aqueous suspension containing 200 g/1 of triticonazole is prepared, containing:
-40% aqueous solution of ethoxylated tristyryl phenol in the potassium phosphate form (dispersing agent) 30 g
- oxyethylenated nonylphenol containing 10 mol of ethylene oxide (wetting agent) 10 g
- propylene glycol 50 g
- polysaccharide (Rhodopol 23) 3 g
- 1,2-benzisothiazolin-3-one (biocide) 1.5 g
- silicone antifoam 3 g
- water q.s. 1000 ml
An imidacloprid composition is used in the form of a commercial formulation of a 70 % aqueous suspension of active material, sold under the trade name Gaucho by the Company Bayer.
The two compositions are applied to the seeds by treatment in a liege bowl apparatus for 30 seconds.
The seeds are sown in a peat/pozzuolana (1:1) substrate contained in 10 cm x 10 cm pots, at a ratio of 10 seeds per pot (there are 4 pots per repetition).
Untreated seeds were sown under the same conditions.
weeks after sowing, the seedlings are infected with a suspension of spores of Puccinia recondita and infested with a population of Aphis so.
Two weeks after contamination, visual inspection is carried out of the activity both against Puccinia recondita and Aphis sp. by comparison with control plants which carry more than 100 Aphis per plant and more than 50 rust pustules per leaf.
The results observed are recorded in the table below:
Active material (a.m.g./q) % effectiveness on
Puccinia recondita % effectiveness on
Aphis sp
Triticonazole | |||||
60 | 90 | 0 | |||
120 | 100 | 0 | |||
180 | 100 | 0 | |||
Imidacloprid | |||||
200 | 0 | more | than | 90 | |
400 | 0 | more | than | 90 | |
Triticonazole | + | ||||
imidacloprid | No. | ||||
60 + 200 | 1 | 90 | more | than | 90 |
60 + 400 | 2 | 90 | more | than | 90 |
120 + 200 | 3 | 100 | more | than | 90 |
120 + 400 | 4 | 100 | more | than | 90 |
180 + 200 | 5 | 100 | more | than | 90 |
180 + 400 | 6 | 100 | more | than | 90 |
Moreover, no phytotoxicity phenomenon was observed. These results clearly show that the combination of the two materials makes it possible to effectively control both brown rust disease on the wheat due to Puccinia recondita and infestation with an insect Aphis sp.
Of course, this example is not limiting and many other diseases and infestations by insects can be treated with the combinations and compositions according to the invention.
This example well illustrates the value of the combinations according to the invention, namely in being able to combine in a single treatment, preferably a seed treatment, the excellent activity of the two active materials, one an insecticide and the other a fungicide, without any harmful interplay.
For practical use, the combinations according to the invention can be used by using compositions containing one or the other of the active materials or both together. In each composition, the active materials are generally used in combination with a solid or liquid vehicle which can be used in agriculture and, optionally, at least one surfaceactive agent.
For their practical use, the constituents of the combination according to the invention are rarely used on their own. Most often they form part of compositions. These compositions, which can be used for the protection of plants against fungal diseases and/or against plant-eating insects or in plant growth regulating compositions, contain, as active material, at least one of the constituents of the combination according to the invention as described above in combination with solid or liquid vehicles which are acceptable in agriculture, and/or surface-active agents which are also acceptable in agriculture. In particular, the usual inert vehicles and the usual surface-active agents can be used.
These compositions generally contain between 0.5 and 95 % of combination according to the invention.
The term vehicle··, in the present account, means a natural or synthetic organic or inorganic material with which the active material is combined in order to facilitate its application to the plant, to seeds or to the soil. The vehicle is therefore generally inert and it has to be acceptable in agriculture, especially to the treated plant. The vehicle can be solid (clays, natural or synthetic silicates, silica, resins, waxes, solid fertilisers, and the like) or liquid (water, alcohol, ketones, petroleum fractions, aromatic or aliphatic hydrocarbons, chlorinated hydrocarbons, liquefied gases, and the like).
The surface-active agent can be an emulsifying, dispersing or wetting agent of ionic or nonionic type. There may be cited, for example, salts of poly(acrylic acids), salts of lignosulphonic acids, salts of phenolsulphonic or naphthalenesulphonic acids, polycondensates of ethylene oxide with fatty alcohols or fatty acids or fatty amines, substituted phenols (especially alkylphenols or arylphenols), salts of esters of sulphosuccinic acids, derivatives of taurine (especially alkyltaurates), and phosphoric esters of polyoxyethylenated alcohols or phenols. The presence of at least one surface-active agent is generally indispensable where the active material and/or the inert vehicle are not soluble in water and where the vector agent of the application is water.
These compositions can also contain all kinds of other ingredients such as, for example, protective colloids, adhesives, thickening agents, thixotropic agents, penetration agents, stabilising agents, sequestering agents and the like, as well as other known active materials possessing pesticidal properties (especially insecticides or fungicides) or possessing properties which promote plant growth (especially fertilisers) or possessing properties which regulate plant growth. More generally, the compounds according to the invention can be used in combination with any of the solid or liquid additives which correspond to the usual formulating techniques.
For their application, the constituents of the combination are thus often in the form of compositions, which are themselves in fairly diverse solid or liquid forms.
There may be mentioned, as solid composition forms, powders for dusting or dispersing (containing the combination according to the invention at a content of up to 100 %) and granules, especially those obtained by extrusion, by compacting, by impregnation of a granulated vehicle, or by granulation from a powder (the content of the combination according to the invention in these granules being between 1 and 80 % for the latter cases).
According to one example of a granular composition, the following constituents are used:
Example G
- combination No.3
- epichlorohydrin
- cetyl polyglycol ether
- polyethylene glycol
- kaolin (particle size:
0.3 to 0.8 mm)
In this particular case, the mixed with the epichlorohydrin and the g
2.5 g 2.5 g g
910 g active materials are mixture is dissolved with 60 g of acetone; polyethylene glycol and cetyl polyglycol ether are then added. The solution obtained is sprayed over the kaolin and the acetone is then evaporated off under vacuum.
Such a microgranule is used advantageously for controlling soil fungi.
The compounds of formula (I) can also be used in the powder form for dusting; it is also possible to use a composition comprising 50 g of active material and 950 g of talc; it is also possible to use a composition comprising 20 g of active material, 10 g of finely divided silica and 970 g of talc; these constituents are mixed and milled and the mixture is applied by dusting.
There may be cited, as liquid composition forms or as forms intended to constitute liquid compositions during application, solutions, in particular water-soluble concentrates, emulsifiable concentrates, emulsions, suspension concentrates, aerosols, wettable powders (or sprayable powder) or pastes.
The emulsifiable or soluble concentrates most often comprise 10 to 80 % of active material, while the ready-toapply solutions or emulsions contain 0.01 to 20 % of active material.
For example, in addition to the solvent, the emulsifiable concentrates can contain, when this is necessary, to 20 % of suitable additives such as the stabilising agents, surface-active agents, penetration agents, corrosion inhibitors, dyes or adhesives mentioned above.
By way of example, the composition of several concentrates will now be given:
EC Example 1
- combination 1 400 g/1
- alkaline dodecylbenzenesulphonate 24 g/1
- oxyethylenated nonylphenol containing molecules of ethylene oxide 16 g/1
- cyclohexanone 200 g/1
- aromatic solvent qs 1 litre
According to another emulsifiable concentrate formula, there are used:
EC Example 2
- combination 2 250 g
- epoxidised vegetable oil 25 g
- mixture of alkylarylsulphonate and of ether of polyglycol and fatty alcohols 100 g
- dimethylformamide 50 g
- xylene 575 g
It is possible, by diluting these concentrates with water, to obtain emulsions of any desired concentration particularly suitable for application to leaves.
The suspension concentrates, which can also be applied by spraying, are prepared so as to produce a stable fluid product which does not settle out and they generally contain from 10 to 75 % of active material, from 0.5 to 15 % of surface-active agents, from 0.1 to 10 % of thixotropic agents, from 0 to 10 % of suitable additives, such as antifoaming agents, corrosion inhibitors, stabilising agents, penetration agents and adhesives and, as vehicle, water or an organic liquid in which the active material has little or no solubility: certain solid organic materials or inorganic salts can be dissolved in the vehicle to help in preventing sedimentation or as antifreeze for water.
Wettable powders (or sprayable powders) are generally prepared so that they contain 20 to 95 % of active material, and they generally contain, in addition to the solid vehicle, from 0 to 5 % of a wetting agent, from 3 to 10 % of a dispersing agent and, when necessary, from 0 to 10 % of one or more stabilising agents and/or other additives, such as penetration agents, adhesives, or anticaking agents, dyes, and the like.
By way of example, various wettable powder compositions will now be given:
WP Example 1:
- combination No. 3 50 %
- calcium lignosulphonate (deflocculating agent) 5 %
- isopropylnaphthalenesulphonate (anionic wetting agent) 1 %
- anticaking silica 5 %
- kaolin (filler) 39 %
Another 70 % sprayable powder composition uses the following constituents:
WP Example 2:
- combination No. 4 700 g
- sodium dibutylnaphthylsulphonate 50 g
- condensation product, in proportions of 3/2/1, of naphthalenesulphonic acid, phenolsulphonic acid and formaldehyde 30 g
- kaolin
100 g
- Champagne chalk 120 g
Another 40 % sprayable powder composition uses the following constituents:
WP Example 3:
- combination No. 5 400 g
- sodium lignosulphonate 50 g
- sodium dibutylnaphthalenesulphonate 10 g
- silica 540 g
Another 25 % sprayable powder composition uses the 10 following constituents:
WP Example 4:
- combination No. 1 250 g
- calcium lignosulphonate 45 g
- equal weight mixture of Champagne chalk and hydroxyethylcellulose 19 g
- sodium dibutylnaphthalenesulphonate 15 g
- silica 195 g
- Champagne chalk 195 g
- kaolin 281 g
Another 25 % sprayable powder composition uses the following constituents:
WP Example 5:
- combination No. 2 250 g
- isooctylphenoxy-polyoxyethylene-ethanol 25 g
- equal weight mixture of Champagne chalk and hydroxyethylcellulose 17 g
- sodium aluminosilicate 543 g
- kieselguhr 165 g
Another 10 % sprayable powder composition uses the
- 12 following constituents:
WP Example 6:
- combination No. 3 100 g
- mixture of sodium salts of sulphates of saturated fatty acids 30 g
- condensation product of naphthalenesulphonic acid and formaldehyde 50 g
- kaolin 820 g
In order to obtain these sprayable powders or wettable powders, the active materials are intimately mixed in suitable mixers with additional substances and the mixture is milled in mills or other suitable grinders. Sprayable powders are thereby obtained whose wettability and suspensibility are advantageous; they can be suspended in water at any desired concentration and these suspensions can be used very advantageously in particular for application to plant leaves.
In place of wettable powders, it is possible to produce pastes. The conditions and methods for producing and using these pastes are similar to those for wettable powders or sprayable powders.
As has already been said, aqueous dispersions and emulsions, for example the compositions obtained by diluting a wettable powder or an emulsifiable concentrate using water according to the invention, are included within the general scope of the present invention. The emulsions can be of waterin-oil or oil-in-water type and they can have a thick consistency like that of a •’mayonnaise.
In the case where the combinations according to the invention are used as fungicides, the usage doses can vary within wide limits, especially depending on the virulence of the fungi and the climatic conditions.
Claims (13)
1. Agrochemical combination for the protection of plants against plant diseases and plant-eating insects, characterised in that it comprises at least an effective quantity of a benzylidene azolyImethylcycloalkane fungicide and at least an effective quantity of the insecticide imidacloprid.
2. Agrochemical combination according to Claim 1, characterised in that the benzylidene azolylmethylcycloalkane fungicide is triticonazole.
3. Combination according to either of Claims 1 and 2, characterised in that each of the active materials is mixed with an inert vehicle and optionally at least one surfaceactive agent.
4. Agrochemical composition for the protection of plants against plant diseases and plant-eating insects, characterised in that it comprises an agrochemical combination based on a benzylidene azolylmethylcycloalkane fungicide and the insecticide imidacloprid in association with a diluent or carrier and, optionally, a surface active agent.
5 characterised in that at least one of the two active materials is applied in seed treatment.
5. Agrochemical composition according to Claim 4, characterised in that the benzylidene azolylmethylcycloalkane fungicide is triticonazole.
6. Process for the treatment of plants in order to protect them against diseases and plant-eating insects, characterised in that an effective quantity of a benzylidene azolyImethylcycloalkane fungicide and an effective quantity of imidacloprid is applied.
7. Process according to Claim 6, characterised in that the two active materials are applied simultaneously.
8. Process according to Claim 7, characterised in that the two active materials are applied successively and conjugately.
9. Process according to one of Claims 6 to 8,
10 il.
Process according to one of Claims 6 to 10, characterised in that triticonazole is applied in a dose of from 2.5 to 250 g per quintal of seed.
10. Process according to one of Claims 6 to 9, characterised in that at least one of the two active materials is applied in soil treatment.
12. Process according to one of Claims 6 to 11, characterised in that imidacloprid is applied in a dose of from
15 25 to 2000 g per quintal of seed.
13. Process according to one of Claims 1 to 12, characterised in that the plant treated is a cereal.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9115397A FR2684519B1 (en) | 1991-12-06 | 1991-12-06 | ASSOCIATION OF A FUNGICIDE FROM THE TRIAZOLES FAMILY AND IMIDACLOPRID. |
Publications (2)
Publication Number | Publication Date |
---|---|
AP9200455A0 AP9200455A0 (en) | 1993-01-31 |
AP351A true AP351A (en) | 1994-08-09 |
Family
ID=9419943
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
APAP/P/1992/000455A AP351A (en) | 1991-12-06 | 1992-12-04 | Mixed agrochemical combination. |
Country Status (24)
Country | Link |
---|---|
EP (1) | EP0545834A1 (en) |
JP (1) | JPH05246806A (en) |
KR (1) | KR930011819A (en) |
CN (1) | CN1072817A (en) |
AP (1) | AP351A (en) |
AU (1) | AU2978992A (en) |
BR (1) | BR9204924A (en) |
CA (1) | CA2084140A1 (en) |
CZ (1) | CZ358292A3 (en) |
FI (1) | FI925532A7 (en) |
FR (1) | FR2684519B1 (en) |
HR (1) | HRP921391A2 (en) |
HU (2) | HU9203846D0 (en) |
IL (1) | IL103923A0 (en) |
MA (1) | MA22728A1 (en) |
MX (1) | MX9206976A (en) |
MY (1) | MY131280A (en) |
NO (1) | NO924677L (en) |
PL (1) | PL296848A1 (en) |
SI (1) | SI9200364A (en) |
SK (1) | SK358292A3 (en) |
TR (1) | TR26842A (en) |
YU (1) | YU104692A (en) |
ZA (1) | ZA929342B (en) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4853798A (en) * | 1983-07-21 | 1989-08-01 | Sony Corporation | Method and apparatus for reproducing digital or analog signals |
FR2711893B1 (en) * | 1993-11-04 | 1996-01-12 | Rhone Poulenc Agrochimie | Association of a fungicide with an azole group with an insecticide with a pyrazole, pyrrole or phenylimidazole group. |
FR2712144B1 (en) * | 1993-11-04 | 1997-07-18 | Rhone Poulenc Agrochimie | Association of a fungicide with an azole group with an insecticide with a pyrazole, pyrrole or phenylimidazole group. |
DE4412833A1 (en) * | 1994-04-14 | 1995-10-19 | Bayer Ag | Insecticidal fertilizer mixtures |
DE4417742A1 (en) * | 1994-05-20 | 1995-11-23 | Bayer Ag | Non-systemic control of parasites |
DE4426753A1 (en) | 1994-07-28 | 1996-02-01 | Bayer Ag | Means for controlling plant pests |
WO1997022254A1 (en) * | 1995-12-18 | 1997-06-26 | Novartis Ag | Pesticidal composition |
DE19829113A1 (en) | 1998-06-10 | 1999-12-16 | Bayer Ag | Means for controlling plant pests |
HU230539B1 (en) | 1998-06-10 | 2016-11-28 | Bayer Intellectual Property Gmbh | Agents for combating plant pests |
ATE278322T1 (en) | 1998-06-17 | 2004-10-15 | Bayer Cropscience Ag | AGENTS FOR CONTROLLING PLANT PESTS |
GB9816638D0 (en) * | 1998-07-30 | 1998-09-30 | Novartis Ag | Organic compounds |
KR101240097B1 (en) * | 2004-06-17 | 2013-03-06 | 바스프 에스이 | Use of (E)-5-(4-chlorobenzylidene)-2,2-dimethyl-1-(1H-1,2,4-triazol-1-yl-methyl)cyclopentanol for controlling rust disease on soybean plants |
CA2673992A1 (en) | 2007-01-19 | 2008-07-24 | Basf Se | Fungicidal mixtures of 1-methylpyrazol-4-ylcarboxanilides and azolopyrimidinylamines |
KR20090105974A (en) * | 2007-01-30 | 2009-10-07 | 바스프 에스이 | Insecticidal mixtures based on azolopyrimidinylamine derivatives and insecticides |
TW200845896A (en) * | 2007-02-06 | 2008-12-01 | Basf Se | Insecticides as safeners for fungicides with phytotoxic activity |
EP3381289B1 (en) | 2007-09-20 | 2021-05-05 | Bayer CropScience LP | Combinations comprising a fungicidal strain and an active compound |
EP2242370A2 (en) * | 2008-02-05 | 2010-10-27 | Basf Se | Pesticidal mixtures |
CN105685082B (en) * | 2012-03-05 | 2018-06-26 | 陕西韦尔奇作物保护有限公司 | A kind of composition pesticide containing triticonazole |
CN103416422A (en) * | 2013-08-31 | 2013-12-04 | 红河蔗保科技有限责任公司 | Sugarcane pesticide and production method thereof |
CN113545343B (en) * | 2021-07-02 | 2022-09-20 | 中化化工科学技术研究总院有限公司 | Spraying auxiliary agent for removing agricultural pest secretion and preparation and use methods thereof |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
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FR2641277A1 (en) * | 1988-12-29 | 1990-07-06 | Rhone Poulenc Agrochimie | Azolylmethylcyclopentanebenzylidene or -cyclopentenebenzylidene and use as fungicide |
DE4111389A1 (en) * | 1991-04-09 | 1992-10-15 | Bayer Ag | Use of imidacloprid as beetle repellent - in molluscicidal formulations, e.g. snail baits |
EP0511541A1 (en) * | 1991-04-27 | 1992-11-04 | Nihon Bayer Agrochem K.K. | Agents for preserving wood or composite-wood materials against insects |
WO1993000009A1 (en) * | 1991-06-26 | 1993-01-07 | Schering Aktiengesellschaft | Pesticidal compositions comprising amitraz and imidacloprid |
US5246953A (en) * | 1990-06-12 | 1993-09-21 | Rhone-Poulenc Secteur Agrochimie | Process for protecting plant propagation products and the plants obtained from them |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MA21706A1 (en) * | 1988-12-29 | 1990-07-01 | Rhone Poulenc Agrochimie | BENZOLIDENE AZOLYLMETHYLCYCLOALCANE AND USE AS A FUNGICIDE. |
JPH03261704A (en) * | 1990-03-12 | 1991-11-21 | Nissan Chem Ind Ltd | Granule for pest control |
-
1991
- 1991-12-06 FR FR9115397A patent/FR2684519B1/en not_active Expired - Fee Related
-
1992
- 1992-11-30 CA CA002084140A patent/CA2084140A1/en not_active Abandoned
- 1992-11-30 IL IL103923A patent/IL103923A0/en unknown
- 1992-12-02 MA MA23018A patent/MA22728A1/en unknown
- 1992-12-02 EP EP92420444A patent/EP0545834A1/en not_active Withdrawn
- 1992-12-02 AU AU29789/92A patent/AU2978992A/en not_active Abandoned
- 1992-12-02 ZA ZA929342A patent/ZA929342B/en unknown
- 1992-12-02 BR BR9204924A patent/BR9204924A/en not_active Application Discontinuation
- 1992-12-03 JP JP4324304A patent/JPH05246806A/en active Pending
- 1992-12-03 MX MX9206976A patent/MX9206976A/en unknown
- 1992-12-03 HR HR921391A patent/HRP921391A2/en not_active Application Discontinuation
- 1992-12-04 PL PL29684892A patent/PL296848A1/en unknown
- 1992-12-04 MY MYPI92002234A patent/MY131280A/en unknown
- 1992-12-04 CZ CS923582A patent/CZ358292A3/en unknown
- 1992-12-04 HU HU9203846A patent/HU9203846D0/en unknown
- 1992-12-04 FI FI925532A patent/FI925532A7/en not_active Application Discontinuation
- 1992-12-04 CN CN92114180A patent/CN1072817A/en active Pending
- 1992-12-04 SI SI19929200364A patent/SI9200364A/en unknown
- 1992-12-04 AP APAP/P/1992/000455A patent/AP351A/en active
- 1992-12-04 HU HU9203846A patent/HUT62756A/en unknown
- 1992-12-04 NO NO92924677A patent/NO924677L/en unknown
- 1992-12-04 YU YU104692A patent/YU104692A/en unknown
- 1992-12-04 SK SK3582-92A patent/SK358292A3/en unknown
- 1992-12-04 TR TR01195/92A patent/TR26842A/en unknown
- 1992-12-05 KR KR1019920023419A patent/KR930011819A/en not_active Withdrawn
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
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FR2641277A1 (en) * | 1988-12-29 | 1990-07-06 | Rhone Poulenc Agrochimie | Azolylmethylcyclopentanebenzylidene or -cyclopentenebenzylidene and use as fungicide |
US5246953A (en) * | 1990-06-12 | 1993-09-21 | Rhone-Poulenc Secteur Agrochimie | Process for protecting plant propagation products and the plants obtained from them |
DE4111389A1 (en) * | 1991-04-09 | 1992-10-15 | Bayer Ag | Use of imidacloprid as beetle repellent - in molluscicidal formulations, e.g. snail baits |
EP0511541A1 (en) * | 1991-04-27 | 1992-11-04 | Nihon Bayer Agrochem K.K. | Agents for preserving wood or composite-wood materials against insects |
WO1993000009A1 (en) * | 1991-06-26 | 1993-01-07 | Schering Aktiengesellschaft | Pesticidal compositions comprising amitraz and imidacloprid |
Also Published As
Publication number | Publication date |
---|---|
NO924677L (en) | 1993-06-07 |
FR2684519B1 (en) | 1994-01-28 |
MY131280A (en) | 2007-07-31 |
PL296848A1 (en) | 1993-08-23 |
EP0545834A1 (en) | 1993-06-09 |
NO924677D0 (en) | 1992-12-04 |
FI925532L (en) | 1993-06-07 |
HUT62756A (en) | 1993-06-28 |
SK358292A3 (en) | 1995-03-08 |
IL103923A0 (en) | 1993-04-04 |
SI9200364A (en) | 1993-06-30 |
AU2978992A (en) | 1993-06-10 |
CA2084140A1 (en) | 1993-06-07 |
CN1072817A (en) | 1993-06-09 |
YU104692A (en) | 1995-10-03 |
AP9200455A0 (en) | 1993-01-31 |
CZ358292A3 (en) | 1993-09-15 |
HRP921391A2 (en) | 1995-12-31 |
TR26842A (en) | 1994-08-19 |
HU9203846D0 (en) | 1993-03-29 |
FI925532A0 (en) | 1992-12-04 |
JPH05246806A (en) | 1993-09-24 |
MX9206976A (en) | 1993-06-01 |
KR930011819A (en) | 1993-07-20 |
ZA929342B (en) | 1993-06-04 |
FR2684519A1 (en) | 1993-06-11 |
MA22728A1 (en) | 1993-07-01 |
BR9204924A (en) | 1993-06-08 |
FI925532A7 (en) | 1993-06-07 |
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