IL29306A - Substituted diphenyl ethers and pesticidal preparations containing them - Google Patents
Substituted diphenyl ethers and pesticidal preparations containing themInfo
- Publication number
- IL29306A IL29306A IL29306A IL2930668A IL29306A IL 29306 A IL29306 A IL 29306A IL 29306 A IL29306 A IL 29306A IL 2930668 A IL2930668 A IL 2930668A IL 29306 A IL29306 A IL 29306A
- Authority
- IL
- Israel
- Prior art keywords
- parts
- active substance
- active
- preparations containing
- diphenyl ethers
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title claims description 10
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 title 1
- 230000000361 pesticidal effect Effects 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims description 6
- 241000607479 Yersinia pestis Species 0.000 claims description 3
- 239000013543 active substance Substances 0.000 description 27
- 239000000203 mixture Substances 0.000 description 10
- 230000001069 nematicidal effect Effects 0.000 description 9
- 239000000126 substance Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 241000244206 Nematoda Species 0.000 description 3
- 238000005266 casting Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 238000010410 dusting Methods 0.000 description 2
- HTAATVDZOHXHBE-UHFFFAOYSA-N methyl 10-formyl-3,9-dihydroxy-1,4,7-trimethyl-6-oxobenzo[b][1,4]benzodioxepine-2-carboxylate Chemical compound O1C2=C(C=O)C(O)=CC(C)=C2C(=O)OC2=C1C(C)=C(C(=O)OC)C(O)=C2C HTAATVDZOHXHBE-UHFFFAOYSA-N 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- UAZUEJTXWAXSMA-UHFFFAOYSA-N 1,1-dichlorobut-1-ene Chemical compound CCC=C(Cl)Cl UAZUEJTXWAXSMA-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- 241000399934 Ditylenchus Species 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- BREXUOXCEDKPCA-UHFFFAOYSA-N [Ca].OB(O)O Chemical compound [Ca].OB(O)O BREXUOXCEDKPCA-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- ZRIUUUJAJJNDSS-UHFFFAOYSA-N ammonium phosphates Chemical class [NH4+].[NH4+].[NH4+].[O-]P([O-])([O-])=O ZRIUUUJAJJNDSS-UHFFFAOYSA-N 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- LWIHDJKSTIGBAC-UHFFFAOYSA-K potassium phosphate Substances [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
- 235000011009 potassium phosphates Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical class [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 235000020681 well water Nutrition 0.000 description 1
- 239000002349 well water Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C255/54—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and etherified hydroxy groups bound to the carbon skeleton
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH88667A CH481571A (de) | 1967-01-20 | 1967-01-20 | Schädlingsbekämpfungsmittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL29306A true IL29306A (en) | 1971-12-29 |
Family
ID=4197461
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL29306A IL29306A (en) | 1967-01-20 | 1968-01-12 | Substituted diphenyl ethers and pesticidal preparations containing them |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3766238A (xx) |
| CH (1) | CH481571A (xx) |
| DE (1) | DE1693192A1 (xx) |
| FR (1) | FR1573898A (xx) |
| GB (1) | GB1189594A (xx) |
| IL (1) | IL29306A (xx) |
| NL (1) | NL6800885A (xx) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3966453A (en) * | 1972-01-27 | 1976-06-29 | Ishihara Sangyo Kaisha Ltd. | Herbicidal 2-halo-4-trifluoromethyl-4'-cyanophenyl-ethers |
| US4046798A (en) * | 1973-02-12 | 1977-09-06 | Rohm And Haas Company | Herbicidal 4-trifluoromethyl-4'nitrodiphenyl ethers |
| US4091109A (en) * | 1976-06-18 | 1978-05-23 | Nippon Kayaku Kabushiki Kaisha | Diphenylether derivatives and use thereof as an acaricide |
| US4350522A (en) * | 1977-06-20 | 1982-09-21 | Rohm And Haas Company | Herbicidal 4-trifluoromethyl-4'-nitrodiphenyl ethers |
| US4332820A (en) * | 1980-01-25 | 1982-06-01 | The Dow Chemical Company | Substituted benzonitriles having antiviral activity |
| US4254144A (en) * | 1980-01-25 | 1981-03-03 | The Dow Chemical Company | Substituted benzonitriles having antiviral activity |
| US4349568A (en) * | 1980-06-12 | 1982-09-14 | The Dow Chemical Company | Sulfur-substituted diphenyl ethers having antiviral activity |
| US4505929A (en) * | 1980-06-12 | 1985-03-19 | The Dow Chemical Company | Sulfur-substituted diphenyl ethers having antiviral activity |
| JPS6341451A (ja) * | 1986-08-06 | 1988-02-22 | Nippon Kayaku Co Ltd | エ−テル誘導体およびそれを有効成分とする殺ダニ、殺虫組成物 |
-
1967
- 1967-01-20 CH CH88667A patent/CH481571A/de not_active IP Right Cessation
-
1968
- 1968-01-11 DE DE19681693192 patent/DE1693192A1/de active Pending
- 1968-01-12 IL IL29306A patent/IL29306A/en unknown
- 1968-01-16 FR FR1573898D patent/FR1573898A/fr not_active Expired
- 1968-01-19 NL NL6800885A patent/NL6800885A/xx unknown
- 1968-01-22 GB GB3193/68A patent/GB1189594A/en not_active Expired
-
1970
- 1970-11-19 US US00091172A patent/US3766238A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| GB1189594A (en) | 1970-04-29 |
| US3766238A (en) | 1973-10-16 |
| CH481571A (de) | 1969-11-30 |
| DE1693192A1 (de) | 1971-06-03 |
| FR1573898A (xx) | 1969-07-11 |
| NL6800885A (xx) | 1968-07-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPS6045508A (ja) | 菌類病害に対するブドウ保護用殺菌剤組成物 | |
| IL29306A (en) | Substituted diphenyl ethers and pesticidal preparations containing them | |
| GB1189931A (en) | Phosphoric and Thionophosphoric Acid Esters, manufacture thereof and their use as Insecticides | |
| US3189428A (en) | Method for inhibiting plant growth | |
| DE1003982B (de) | Schaedlingsbekaempfungsmittel | |
| IL29305A (en) | Pesticidal preparations containing diaralkyl amines | |
| DE1817662B2 (de) | N,N-Diäthyl-S-(4-chlorbenzyl)thiocarbamat und seine Verwendung | |
| US2954318A (en) | Miticide composition | |
| US3008869A (en) | Nematocide compositions | |
| US2934420A (en) | Pesticidal and herbicidal compositions of matter | |
| US2367534A (en) | Parasiticides | |
| US2940896A (en) | Quaternary ammonium and phosphoramide ester attractants and insect control therewith | |
| US5073647A (en) | Reduction and inhibition of etu content in alkylenebisdithiocarbamates | |
| RU2780679C1 (ru) | Фунгицидная композиция | |
| DE1301819B (de) | Substituierte 2, 4-Diamino-6-chlor-s-triazine | |
| US3700778A (en) | Insecticidal composition containing trifluoromethyl substituted benzanilides and method of using the same | |
| SU537611A3 (ru) | Гербицидный состав | |
| DE944404C (de) | Insektenbekaempfungsmittel | |
| DE1445824B1 (de) | 1,3,4-Thiadiazolderivate und ihre Verwendung als nematozide Mittel | |
| DE1445824C (xx) | ||
| DE2141227A1 (de) | Carbamoyloximverbindungen sowie deren Verwendung | |
| US3129136A (en) | Controlling nematodes with 2-chloro-3-hydroxy-4-nitro-benzaldehyde | |
| US3810982A (en) | Insecticidal phosphonyl cyanodithioimido carbonates | |
| EP0092632B1 (de) | Neue Benzonitrilderivate, Verfahren zu ihrer Herstellung und herbicide Mittel | |
| US3482921A (en) | Compositions of copper(i) cyanide and alkali metal salts and agents containing same for controlling aquatic insects |