FI62828C - Insekticida bentsoylureidodifenyletrar - Google Patents
Insekticida bentsoylureidodifenyletrar Download PDFInfo
- Publication number
- FI62828C FI62828C FI762042A FI762042A FI62828C FI 62828 C FI62828 C FI 62828C FI 762042 A FI762042 A FI 762042A FI 762042 A FI762042 A FI 762042A FI 62828 C FI62828 C FI 62828C
- Authority
- FI
- Finland
- Prior art keywords
- ethers
- larvae
- active ingredient
- isocyanate
- benzoyl
- Prior art date
Links
- 239000000460 chlorine Substances 0.000 description 38
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
- 239000004480 active ingredient Substances 0.000 description 15
- 238000002360 preparation method Methods 0.000 description 14
- 239000002904 solvent Substances 0.000 description 14
- -1 benzoyl ureido diphenyl ethers Chemical class 0.000 description 12
- 238000000034 method Methods 0.000 description 11
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 9
- 239000003995 emulsifying agent Substances 0.000 description 8
- 150000002170 ethers Chemical class 0.000 description 8
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- 239000013543 active substance Substances 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 241000255925 Diptera Species 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
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- 230000000749 insecticidal effect Effects 0.000 description 5
- GYNAVKULVOETAD-UHFFFAOYSA-N n-phenoxyaniline Chemical compound C=1C=CC=CC=1NOC1=CC=CC=C1 GYNAVKULVOETAD-UHFFFAOYSA-N 0.000 description 5
- 229920000151 polyglycol Polymers 0.000 description 5
- 239000010695 polyglycol Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical class CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
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- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
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- KGGHWIKBOIQEAJ-UHFFFAOYSA-N 2-fluorobenzamide Chemical compound NC(=O)C1=CC=CC=C1F KGGHWIKBOIQEAJ-UHFFFAOYSA-N 0.000 description 3
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- 241001674044 Blattodea Species 0.000 description 3
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 description 3
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- 125000002877 alkyl aryl group Chemical group 0.000 description 3
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 3
- 150000008052 alkyl sulfonates Chemical class 0.000 description 3
- 229940054066 benzamide antipsychotics Drugs 0.000 description 3
- 150000003936 benzamides Chemical class 0.000 description 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 3
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- 241001327638 Cimex lectularius Species 0.000 description 2
- 241001641895 Dermestes Species 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 241000255896 Galleria mellonella Species 0.000 description 2
- 241000257303 Hymenoptera Species 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
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- 239000003513 alkali Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
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- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- GRUHREVRSOOQJG-UHFFFAOYSA-N 2,4-dichlorobenzonitrile Chemical compound ClC1=CC=C(C#N)C(Cl)=C1 GRUHREVRSOOQJG-UHFFFAOYSA-N 0.000 description 1
- 125000004098 2,6-dichlorobenzoyl group Chemical group O=C([*])C1=C(Cl)C([H])=C([H])C([H])=C1Cl 0.000 description 1
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 1
- YYHJASKQCZDYMM-UHFFFAOYSA-N 2-chloro-4-(2,6-dichloro-4-isocyanatophenoxy)benzonitrile Chemical compound ClC1=CC(N=C=O)=CC(Cl)=C1OC1=CC=C(C#N)C(Cl)=C1 YYHJASKQCZDYMM-UHFFFAOYSA-N 0.000 description 1
- PMIVDSUKSGSURV-UHFFFAOYSA-N 4-(4-amino-2,6-dichlorophenoxy)-2-chlorobenzonitrile Chemical compound ClC1=CC(N)=CC(Cl)=C1OC1=CC=C(C#N)C(Cl)=C1 PMIVDSUKSGSURV-UHFFFAOYSA-N 0.000 description 1
- QMXKJLUXIMTNCX-UHFFFAOYSA-N 6-bromo-6-methylcyclohexa-2,4-diene-1-carbonyl isocyanate Chemical compound BrC1(C(C(=O)N=C=O)C=CC=C1)C QMXKJLUXIMTNCX-UHFFFAOYSA-N 0.000 description 1
- WPNROXVJLHEQOX-UHFFFAOYSA-N 6-bromo-6-methylcyclohexa-2,4-diene-1-carboxamide Chemical compound BrC1(C(C(=O)N)C=CC=C1)C WPNROXVJLHEQOX-UHFFFAOYSA-N 0.000 description 1
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- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
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- 238000005684 Liebig rearrangement reaction Methods 0.000 description 1
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- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
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- 235000001535 Ribes X utile Nutrition 0.000 description 1
- 235000016919 Ribes petraeum Nutrition 0.000 description 1
- 244000281247 Ribes rubrum Species 0.000 description 1
- 235000002355 Ribes spicatum Nutrition 0.000 description 1
- 241000256251 Spodoptera frugiperda Species 0.000 description 1
- 241000985245 Spodoptera litura Species 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 241000254109 Tenebrio molitor Species 0.000 description 1
- 241001454295 Tetranychidae Species 0.000 description 1
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- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
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- 239000002969 artificial stone Substances 0.000 description 1
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- 150000008047 benzoylureas Chemical class 0.000 description 1
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- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 150000008422 chlorobenzenes Chemical class 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
- 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
- 238000001035 drying Methods 0.000 description 1
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- 235000013399 edible fruits Nutrition 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
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- 229940052303 ethers for general anesthesia Drugs 0.000 description 1
- DXVYLFHTJZWTRF-UHFFFAOYSA-N ethyl iso-butyl ketone Natural products CCC(=O)CC(C)C DXVYLFHTJZWTRF-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- YYJNOYZRYGDPNH-MFKUBSTISA-N fenpyroximate Chemical compound C=1C=C(C(=O)OC(C)(C)C)C=CC=1CO/N=C/C=1C(C)=NN(C)C=1OC1=CC=CC=C1 YYJNOYZRYGDPNH-MFKUBSTISA-N 0.000 description 1
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- 239000004088 foaming agent Substances 0.000 description 1
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- 150000008282 halocarbons Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- FJIKWRGCXUCUIG-UHFFFAOYSA-N lormetazepam Chemical compound N=1C(O)C(=O)N(C)C2=CC=C(Cl)C=C2C=1C1=CC=CC=C1Cl FJIKWRGCXUCUIG-UHFFFAOYSA-N 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
- 238000002156 mixing Methods 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
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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
- A01N47/08—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 one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/46—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylureas
- C07C275/48—Y being a hydrogen or a carbon atom
- C07C275/54—Y being a carbon atom of a six-membered aromatic ring, e.g. benzoylureas
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2531743A DE2531743C2 (de) | 1975-07-16 | 1975-07-16 | 2',3,6'-Trichlor-4-cyano-4'-benzoylureido- diphenyläther, Verfahren zu ihrer Herstellung und ihre Verwenung als Insektizide |
| DE2531743 | 1975-07-16 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI762042A FI762042A (de) | 1977-01-17 |
| FI62828B FI62828B (fi) | 1982-11-30 |
| FI62828C true FI62828C (fi) | 1983-03-10 |
Family
ID=5951637
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI762042A FI62828C (fi) | 1975-07-16 | 1976-07-14 | Insekticida bentsoylureidodifenyletrar |
Country Status (36)
| Country | Link |
|---|---|
| US (1) | US4064267A (de) |
| JP (1) | JPS594424B2 (de) |
| AR (1) | AR209503A1 (de) |
| AT (1) | AT346650B (de) |
| BE (1) | BE844066A (de) |
| BG (1) | BG24799A3 (de) |
| BR (1) | BR7604616A (de) |
| CA (1) | CA1067516A (de) |
| CH (1) | CH598756A5 (de) |
| CS (1) | CS193554B2 (de) |
| DD (1) | DD131712A5 (de) |
| DE (1) | DE2531743C2 (de) |
| DK (1) | DK319676A (de) |
| EG (1) | EG13754A (de) |
| ES (1) | ES449843A1 (de) |
| FI (1) | FI62828C (de) |
| FR (1) | FR2318153A1 (de) |
| GB (1) | GB1488644A (de) |
| GR (1) | GR60791B (de) |
| HU (1) | HU176058B (de) |
| IE (1) | IE43394B1 (de) |
| IL (1) | IL50031A (de) |
| IT (1) | IT1062525B (de) |
| KE (1) | KE3019A (de) |
| LU (1) | LU75381A1 (de) |
| MY (1) | MY8000262A (de) |
| NL (1) | NL7607857A (de) |
| NO (1) | NO149384C (de) |
| OA (1) | OA05379A (de) |
| PH (1) | PH12694A (de) |
| PL (1) | PL98701B1 (de) |
| PT (1) | PT65359B (de) |
| RO (1) | RO72547A (de) |
| SE (1) | SE421414B (de) |
| TR (1) | TR19158A (de) |
| ZA (1) | ZA764194B (de) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TR19459A (tr) * | 1976-08-25 | 1979-05-01 | Bayer Ag | Suebstitueye benzoliuereidodifenil eterleri,bunlarin hazirlanisi icin usuller ve bunlarin ensektisidler olarak kullanilmalari |
| ZA793186B (en) * | 1978-07-06 | 1981-02-25 | Duphar Int Res | New urea and thiourea compounds, method of preparing the new compounds, as well as insecticidal compositions on the basis of these compounds |
| US4505931A (en) * | 1979-02-01 | 1985-03-19 | Ciba-Geigy Corporation | Pesticidal N-(4-alkenylthio)-phenyl-N'-benzoylureas |
| US4339460A (en) | 1979-02-01 | 1982-07-13 | Ciba-Geigy Corporation | Pesticidal N-[4-(3'-bromoallyloxy)-phenyl]-N'-benzoyl ureas |
| US4310548A (en) | 1979-02-01 | 1982-01-12 | Ciba-Geigy Corporation | Pesticidal N-tetrafluorophenyl-N'-benzoyl ureas |
| US4880838A (en) * | 1982-06-30 | 1989-11-14 | Rhone-Poulenc | Pesticidal 1-(4-Phenoxyphenyl)-5-Benzoyl urea compounds and process for preparation |
| US4529819A (en) * | 1982-08-02 | 1985-07-16 | The Dow Chemical Company | Method for making benzoylphenylureas |
| DE3232265A1 (de) * | 1982-08-31 | 1984-03-01 | Basf Ag, 6700 Ludwigshafen | N-benzoyl-n'-phenoxyphenylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung von schaedlingen |
| US5166179A (en) * | 1982-08-31 | 1992-11-24 | Arno Lange | N-benzoyl-N'-phenoxyphenylureas, their preparation and their use for controlling pests |
| US4659724A (en) * | 1982-12-30 | 1987-04-21 | Union Carbide Corporation | Certain 1-[4-(5-cyano-2-pyridyloxy)phenyl-benzoyl ureas having pesticidal properties |
| US4560770A (en) * | 1983-02-09 | 1985-12-24 | Ciba-Geigy Corporation | Pesticidal compositions based on N-pyrrolylphenyl-N'-benzoylurea compounds |
| US4873264A (en) * | 1983-05-20 | 1989-10-10 | Rhone-Poulenc Nederlands B.V. | Novel pesticidal 1-(alkyl-phenoxy-aryl)-3-benzoyl ureas and process for preparation |
| US5135953A (en) * | 1984-12-28 | 1992-08-04 | Ciba-Geigy | Use of acyl urea compounds for controlling endoparasites and ectoparasites of warm-blooded animals |
| AU602060B2 (en) * | 1987-04-03 | 1990-09-27 | Sumitomo Chemical Company, Limited | A benzoylurea derivative and its production and use, and aniline intermediates therefor |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2438747C2 (de) * | 1974-08-13 | 1982-10-14 | Bayer Ag, 5090 Leverkusen | Benzoylureido-diphenyläther, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide |
-
1975
- 1975-07-16 DE DE2531743A patent/DE2531743C2/de not_active Expired
-
1976
- 1976-07-01 NO NO762307A patent/NO149384C/no unknown
- 1976-07-06 RO RO7686831A patent/RO72547A/ro unknown
- 1976-07-06 HU HU76BA3430A patent/HU176058B/hu unknown
- 1976-07-07 EG EG411/76A patent/EG13754A/xx active
- 1976-07-07 CS CS764506A patent/CS193554B2/cs unknown
- 1976-07-08 OA OA55877A patent/OA05379A/xx unknown
- 1976-07-12 US US05/704,708 patent/US4064267A/en not_active Expired - Lifetime
- 1976-07-12 BG BG033724A patent/BG24799A3/xx unknown
- 1976-07-13 IL IL50031A patent/IL50031A/xx unknown
- 1976-07-13 BE BE168857A patent/BE844066A/xx not_active IP Right Cessation
- 1976-07-13 PT PT65359A patent/PT65359B/pt unknown
- 1976-07-13 CH CH899076A patent/CH598756A5/xx not_active IP Right Cessation
- 1976-07-13 PH PH18684A patent/PH12694A/en unknown
- 1976-07-14 LU LU75381A patent/LU75381A1/xx unknown
- 1976-07-14 FI FI762042A patent/FI62828C/fi not_active IP Right Cessation
- 1976-07-14 IT IT25321/76A patent/IT1062525B/it active
- 1976-07-14 GR GR51267A patent/GR60791B/el unknown
- 1976-07-14 DD DD7600193849A patent/DD131712A5/de unknown
- 1976-07-14 TR TR19158A patent/TR19158A/xx unknown
- 1976-07-14 GB GB29331/76A patent/GB1488644A/en not_active Expired
- 1976-07-15 BR BR7604616A patent/BR7604616A/pt unknown
- 1976-07-15 NL NL7607857A patent/NL7607857A/xx not_active Application Discontinuation
- 1976-07-15 IE IE1559/76A patent/IE43394B1/en unknown
- 1976-07-15 SE SE7608100A patent/SE421414B/xx unknown
- 1976-07-15 DK DK319676A patent/DK319676A/da not_active Application Discontinuation
- 1976-07-15 PL PL1976191211A patent/PL98701B1/zh unknown
- 1976-07-15 ES ES449843A patent/ES449843A1/es not_active Expired
- 1976-07-15 CA CA257,094A patent/CA1067516A/en not_active Expired
- 1976-07-15 ZA ZA764194A patent/ZA764194B/xx unknown
- 1976-07-16 AR AR263969A patent/AR209503A1/es active
- 1976-07-16 FR FR7621844A patent/FR2318153A1/fr active Granted
- 1976-07-16 JP JP51084079A patent/JPS594424B2/ja not_active Expired
- 1976-07-16 AT AT524876A patent/AT346650B/de not_active IP Right Cessation
-
1980
- 1980-01-25 KE KE3019A patent/KE3019A/xx unknown
- 1980-12-30 MY MY262/80A patent/MY8000262A/xx unknown
Also Published As
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed |
Owner name: BAYER AKTIENGESELLSCHAFT |