EP0000388B1 - Pyridazinon(thiono)-phosphorsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide und Akarizide - Google Patents
Pyridazinon(thiono)-phosphorsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide und Akarizide Download PDFInfo
- Publication number
- EP0000388B1 EP0000388B1 EP78100345A EP78100345A EP0000388B1 EP 0000388 B1 EP0000388 B1 EP 0000388B1 EP 78100345 A EP78100345 A EP 78100345A EP 78100345 A EP78100345 A EP 78100345A EP 0000388 B1 EP0000388 B1 EP 0000388B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- spp
- thiono
- butyl
- preparation
- propyl
- Prior art date
- Legal status (The legal status 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 status listed.)
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- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 241001065719 Tetranychus ludeni Species 0.000 description 1
- 241001454293 Tetranychus urticae Species 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 241000254086 Tribolium <beetle> Species 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical group ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
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- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 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
- 244000000054 animal parasite Species 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- MVEKXQBZICSLMC-UHFFFAOYSA-N butan-2-yl ethoxy hydrogen phosphate Chemical compound C(C)OOP(OC(C)CC)(O)=O MVEKXQBZICSLMC-UHFFFAOYSA-N 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 150000008422 chlorobenzenes Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 244000078703 ectoparasite Species 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- 238000002474 experimental method 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
- 235000013312 flour Nutrition 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical class [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000004579 marble Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- SYBYTAAJFKOIEJ-UHFFFAOYSA-N methyl iso-propyl ketone Natural products CC(C)C(C)=O SYBYTAAJFKOIEJ-UHFFFAOYSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 230000003071 parasitic effect Effects 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 239000001007 phthalocyanine dye Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- PECRFPZAFZIMEN-UHFFFAOYSA-N propan-2-ylhydrazine;sulfuric acid Chemical compound CC(C)NN.OS(O)(=O)=O PECRFPZAFZIMEN-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing heterocyclic radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6509—Six-membered rings
- C07F9/650905—Six-membered rings having the nitrogen atoms in the positions 1 and 2
Definitions
- the present invention relates to new pyridazinone (thiono) phosphoric acid esters, a process for their preparation and their use as insecticides and acaricides.
- O, O-dialkyl-O-pyridazinyl thionophosphoric acid esters e.g. O, O-diethyl-0- (1-phenyl-1,6-di-hydro-pyridaz (6) on (3) yl) -thionophosphoric acid esters are characterized by insecticidal and acaricidal activity (see US Pat. No. 2,759,937).
- Japanese patent application 74 12 702 0.0-dialkyl-0-3 (N-methyl-6-pyridazinonyl) (thiono) phosphoric acid ester with insecticidal properties is known.
- the pyridazinone (thiono) phosphoric acid esters mentioned at the beginning and described in more detail below are, as shown by comparative experiments, unexpectedly superior to the known structurally similar phosphoric acid esters as insecticides and acaricides.
- the pyridazinone (thiono) phosphoric acid esters (I) according to the invention have better insecticidal and acaricidal activity than the previously known compounds of analogous constitution and the same direction of action.
- the products according to the present invention thus represent a real enrichment of the technology.
- the 1,6-dihydro-3-hydroxy-1-iso-propyl-pyridazin (6) on (III) which is also to be used as the starting material can also be prepared by processes known from the literature.
- the process for the preparation of the compounds according to the invention is preferably carried out using suitable solvents or diluents.
- suitable solvents or diluents include in particular aliphatic and aromatic, optionally chlorinated hydrocarbons, such as benzene, toluene, xylene, gasoline, methylene chloride, chloroform, carbon tetrachloride, chlorobenzene, or ether, e.g. Diethyl and dibutyl ether, dioxane, also ketones, for example acetone, methyl ethyl, methyl isopropyl and methyl isobutyl ketone, and also nitriles, such as aceto and propionitrile.
- chlorinated hydrocarbons such as benzene, toluene, xylene, gasoline, methylene chloride, chloroform, carbon tetrachloride, chlorobenzene, or ether, e.g. Diethyl
- All customary acid binders can be used as acid acceptors.
- Alkali carbonates and alcoholates such as sodium and potassium carbonate, methylate or ethylate, and also aliphatic, aromatic or heterocyclic amines, for example trimethylamine, triethylamine, dimethylaniline, dimethylbenzylamine and pyridine, have proven particularly useful.
- the reaction temperature can be varied within a wide range. Generally one works between 0 and 100 ° C, preferably at 20 to 60 ° C.
- the reaction is generally allowed to proceed at normal pressure.
- the starting components are preferably used in equivalent ratios.
- An excess of one or the other component has no significant advantages.
- the reaction components are generally combined in one of the specified solvents and are usually stirred at elevated temperature for one or more hours to complete the reaction. Then an organic solvent is added, e.g. Toiuol, and works up the organic phase as usual by washing, drying and distilling off the solvent.
- the new compounds are obtained in the form of oils, which usually cannot be distilled without decomposing, but by so-called “distillation", i.e. can be freed from the last volatile constituents by prolonged heating under reduced pressure to moderately elevated temperatures and can be cleaned in this way.
- the refractive index is used to characterize them.
- the pyridazinone (thiono) phosphoric acid esters according to the invention are notable for excellent insecticidal and acaricidal activity. They act not only against plant, hygiene and storage pests, but also in the veterinary medical sector against animal parasites (ectoparasites), such as parasitic fly larvae. With low phytoxicity, the compounds have both a good action against sucking and eating insects and mites.
- the compounds according to the invention can be successfully used as pesticides in crop protection and in the hygiene, stored product protection and veterinary sectors.
- the active ingredients can be converted into the customary formulations, such as solutions, emulsions, wettable powders, suspensions, powders, dusts, foams, pastes, soluble powders, granules, aerosols, suspension emulsion concentrates, seed powders, active ingredient-impregnated natural and synthetic substances, very fine encapsulations in polymeric substances and in coating compositions for seeds, also in formulations with fuel sets, such as smoking cartridges, cans, spirals, etc., as well as ULV cold and warm mist formulations.
- customary formulations such as solutions, emulsions, wettable powders, suspensions, powders, dusts, foams, pastes, soluble powders, granules, aerosols, suspension emulsion concentrates, seed powders, active ingredient-impregnated natural and synthetic substances, very fine encapsulations in polymeric substances and in coating compositions for seeds, also in formulations with fuel sets, such as smoking cartridges, cans, spirals, etc.,
- formulations are prepared in a known manner, for example by mixing the active ingredients with extenders, that is to say liquid solvents, pressurized liquefied gases and / or solid carriers, if appropriate using surface-active agents, that is to say emulsifiers and / or dispersants and / or foam-generating agents. If water is used as an extender, organic solvents can, for example, also be used as auxiliary solvents.
- extenders that is to say liquid solvents, pressurized liquefied gases and / or solid carriers, if appropriate using surface-active agents, that is to say emulsifiers and / or dispersants and / or foam-generating agents.
- surface-active agents that is to say emulsifiers and / or dispersants and / or foam-generating agents.
- organic solvents can, for example, also be used as auxiliary solvents.
- liquid solvents aromatics, such as xylene, toluene, or alkylnaphthalenes, chlorinated aromatics or chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chloroethylene or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, for example petroleum fractions, alcohols, such as butanol or glycol, and the like Ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethylformamide and dimethyl sulfoxide, and water;
- Liquefied gaseous extenders or carriers mean those liquids which are gaseous at normal temperature and under normal pressure, for example aerosol propellants, such as halogenated hydrocarbons and butane, propane, nitrogen and carbon dioxide; as solid carriers; natural rock powders, such as
- Adhesives such as carboxymethyl cellulose and natural and synthetic polymers in the form of powders, granules or latices, such as gum arabic, polyvinyl alcohol and polyvinyl acetate, can be used in the formulations.
- Dyes such as inorganic pigments, e.g. Iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarin, azo metal phthalocyanine dyes and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc can be used.
- the formulations generally contain between 0.1 and 95 percent by weight of active compound, preferably between 0.5 and 90%.
- the active compounds according to the invention are used in the form of their commercially available formulations and / or the use forms prepared from these formulations.
- the active substance content of the use forms prepared from the commercially available formulations can vary within wide ranges.
- the active substance concentration of the use forms can be from 0.0000001 to 100% by weight of active substance, preferably between 0.01 and 10% by weight.
- the application takes place in a customary manner adapted to the application forms.
- the active ingredients When used against hygiene pests and pests of stored products, the active ingredients are distinguished by an excellent residual action on wood and clay and by a good stability to alkali on limed substrates.
- Emulsifier 1 part by weight of alkylaryl polyglycol ether
- active compound 1 part by weight of active compound is mixed with the stated amount of solvent and the stated amount of emulsifier, and the concentrate is diluted with water to the desired concentration.
- Cabbage plants (Brassica oleracea), which are heavily infested with peach aphids (Myzus persicae), are sprayed to runoff point with the active substance preparation.
- the kill is determined in%. 100% means that all aphids have been killed; 0% means that no aphids have been killed.
- Emulsifier 1 part by weight of alkylaryl polyglycol ether
- active compound 1 part by weight of active compound is mixed with the stated amount of solvent and the stated amount of emulsifier, and the concentrate is diluted with water to the desired concentration.
- Bean plants Phaseolus vulgaris which are heavily infested with all stages of development of the common spider mite or bean spider mite (Tetranychus urticae) are sprayed to runoff point with the preparation of active compound.
- the kill is determined in%. 100% means that all spider mites have been killed; 0% means that no spider mites have been killed.
- the 1-isopropyl-1,6-dihydro-3-hydroxy-6-oxopyridazine to be used as the starting material can be prepared, for example, as follows:
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19772732101 DE2732101A1 (de) | 1977-07-15 | 1977-07-15 | Pyridazinon(thiono)-phosphorsaeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide |
DE2732101 | 1977-07-15 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0000388A1 EP0000388A1 (de) | 1979-01-24 |
EP0000388B1 true EP0000388B1 (de) | 1980-11-26 |
Family
ID=6014045
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP78100345A Expired EP0000388B1 (de) | 1977-07-15 | 1978-07-11 | Pyridazinon(thiono)-phosphorsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide und Akarizide |
Country Status (19)
Country | Link |
---|---|
US (1) | US4219546A (cs) |
EP (1) | EP0000388B1 (cs) |
JP (1) | JPS5419988A (cs) |
AR (1) | AR218924A1 (cs) |
AT (1) | AT354812B (cs) |
AU (1) | AU514922B2 (cs) |
BR (1) | BR7804540A (cs) |
CA (1) | CA1099270A (cs) |
CS (1) | CS207631B2 (cs) |
DE (2) | DE2732101A1 (cs) |
DK (1) | DK318478A (cs) |
EG (1) | EG13407A (cs) |
ES (1) | ES471749A1 (cs) |
IL (1) | IL55123A (cs) |
IT (1) | IT7825663A0 (cs) |
NZ (1) | NZ187841A (cs) |
PT (1) | PT68271A (cs) |
TR (1) | TR19756A (cs) |
ZA (1) | ZA784027B (cs) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4571397A (en) * | 1982-03-05 | 1986-02-18 | Nissan Chemical Industries | Pyridazinone derivatives, preparation thereof, and agricultural and horticultural fungicidal, insecticidal, acaricidal, nematicidal compositions containing said derivatives |
JPH0350221U (cs) * | 1989-09-22 | 1991-05-16 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL93954C (cs) * | 1955-03-21 | 1900-01-01 | ||
US3100206A (en) * | 1961-05-05 | 1963-08-06 | Dow Chemical Co | O-(1,6-dihydro-6-oxo - 3 - pyridazinyl) o - alkyl phosphoramidate and phosphoramidothioate |
CH507304A (de) * | 1968-03-27 | 1971-05-15 | Bayer Ag | Verfahren zur Herstellung von Thionophosphonsäureestern |
JPS4912702B1 (cs) * | 1970-09-11 | 1974-03-26 | ||
DE2343741A1 (de) * | 1973-08-30 | 1975-03-20 | Bayer Ag | 0-aethyl-s-0- eckige klammer auf pyridaz-(3)-on-(6)-yl eckige klammer zu -thionothiolphosphorsaeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide |
DE2531340A1 (de) * | 1975-07-12 | 1977-01-27 | Bayer Ag | O-aethyl-o-pyridazinylthionobenzolphosphonsaeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide |
DE2603993A1 (de) * | 1976-02-03 | 1977-08-04 | Bayer Ag | (thiono)(thiol)pyridazinphosphor (phosphon)-saeureester bzw. -esteramide, verfahren zu ihrer herstellung sowie ihre verwendung als insektizide und akarizide |
-
1977
- 1977-07-15 DE DE19772732101 patent/DE2732101A1/de not_active Withdrawn
-
1978
- 1978-06-29 US US05/920,506 patent/US4219546A/en not_active Expired - Lifetime
- 1978-07-10 PT PT68271A patent/PT68271A/pt unknown
- 1978-07-11 DE DE7878100345T patent/DE2860340D1/de not_active Expired
- 1978-07-11 EP EP78100345A patent/EP0000388B1/de not_active Expired
- 1978-07-11 CS CS784647A patent/CS207631B2/cs unknown
- 1978-07-12 IL IL55123A patent/IL55123A/xx unknown
- 1978-07-12 TR TR19756A patent/TR19756A/xx unknown
- 1978-07-12 NZ NZ187841A patent/NZ187841A/xx unknown
- 1978-07-12 AU AU37959/78A patent/AU514922B2/en not_active Expired
- 1978-07-13 IT IT7825663A patent/IT7825663A0/it unknown
- 1978-07-13 CA CA307,314A patent/CA1099270A/en not_active Expired
- 1978-07-13 JP JP8460378A patent/JPS5419988A/ja active Pending
- 1978-07-14 AR AR272959A patent/AR218924A1/es active
- 1978-07-14 ZA ZA00784027A patent/ZA784027B/xx unknown
- 1978-07-14 DK DK783184A patent/DK318478A/da unknown
- 1978-07-14 AT AT510578A patent/AT354812B/de not_active IP Right Cessation
- 1978-07-14 BR BR7804540A patent/BR7804540A/pt unknown
- 1978-07-14 ES ES471749A patent/ES471749A1/es not_active Expired
- 1978-07-15 EG EG441/78A patent/EG13407A/xx active
Also Published As
Publication number | Publication date |
---|---|
AR218924A1 (es) | 1980-07-15 |
EG13407A (en) | 1982-03-31 |
JPS5419988A (en) | 1979-02-15 |
IT7825663A0 (it) | 1978-07-13 |
IL55123A (en) | 1982-05-31 |
BR7804540A (pt) | 1979-03-06 |
ATA510578A (de) | 1979-06-15 |
DE2860340D1 (en) | 1981-02-12 |
CS207631B2 (en) | 1981-08-31 |
PT68271A (de) | 1978-08-01 |
DE2732101A1 (de) | 1979-01-25 |
US4219546A (en) | 1980-08-26 |
TR19756A (tr) | 1979-11-30 |
EP0000388A1 (de) | 1979-01-24 |
NZ187841A (en) | 1980-04-28 |
AU514922B2 (en) | 1981-03-05 |
ZA784027B (en) | 1979-07-25 |
ES471749A1 (es) | 1979-02-01 |
CA1099270A (en) | 1981-04-14 |
AU3795978A (en) | 1980-01-17 |
IL55123A0 (en) | 1978-09-29 |
DK318478A (da) | 1979-01-16 |
AT354812B (de) | 1979-01-25 |
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