DE1121882B - Schaedlingsbekaempfungsmittel mit insektizider und akarizider Wirkung - Google Patents
Schaedlingsbekaempfungsmittel mit insektizider und akarizider WirkungInfo
- Publication number
- DE1121882B DE1121882B DEF25209A DEF0025209A DE1121882B DE 1121882 B DE1121882 B DE 1121882B DE F25209 A DEF25209 A DE F25209A DE F0025209 A DEF0025209 A DE F0025209A DE 1121882 B DE1121882 B DE 1121882B
- Authority
- DE
- Germany
- Prior art keywords
- spider mites
- sch
- aphids
- effect
- phenyl
- 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.)
- Pending
Links
- 230000000749 insecticidal effect Effects 0.000 title claims description 7
- 230000000895 acaricidal effect Effects 0.000 title claims description 3
- 241000607479 Yersinia pestis Species 0.000 title 1
- 230000002940 repellent Effects 0.000 title 1
- 239000005871 repellent Substances 0.000 title 1
- 241001454295 Tetranychidae Species 0.000 claims description 35
- 241001124076 Aphididae Species 0.000 claims description 25
- 239000004480 active ingredient Substances 0.000 claims description 7
- 230000004071 biological effect Effects 0.000 claims description 7
- 230000003151 ovacidal effect Effects 0.000 claims description 7
- 239000000575 pesticide Substances 0.000 claims description 6
- 230000001988 toxicity Effects 0.000 claims description 6
- 231100000419 toxicity Toxicity 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 241000256113 Culicidae Species 0.000 claims description 4
- 239000004606 Fillers/Extenders Substances 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Chemical compound OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 claims description 2
- 150000003139 primary aliphatic amines Chemical class 0.000 claims description 2
- 150000005619 secondary aliphatic amines Chemical class 0.000 claims description 2
- 208000024891 symptom Diseases 0.000 claims description 2
- 241000255925 Diptera Species 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 24
- -1 phenyl-thionophosphoric acid ester amides Chemical class 0.000 description 13
- 230000009885 systemic effect Effects 0.000 description 11
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
- 230000000694 effects Effects 0.000 description 9
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- 238000001816 cooling Methods 0.000 description 7
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 5
- 239000003208 petroleum Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000007795 chemical reaction product Substances 0.000 description 4
- 150000001470 diamides Chemical class 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 241000118205 Ovicides Species 0.000 description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 235000019270 ammonium chloride Nutrition 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- 241000257161 Calliphoridae Species 0.000 description 2
- 241000736227 Lucilia sericata Species 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical compound OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 2
- 125000004414 alkyl thio group Chemical group 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 241001221110 Eriophyidae Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 125000005265 dialkylamine group Chemical group 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- BGMIRDHBNWQSGE-UHFFFAOYSA-N hypochlorous acid;pyridine Chemical compound ClO.C1=CC=NC=C1 BGMIRDHBNWQSGE-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- WQYSXVGEZYESBR-UHFFFAOYSA-N thiophosphoryl chloride Chemical compound ClP(Cl)(Cl)=S WQYSXVGEZYESBR-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- 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
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/22—Amides of acids of phosphorus
- C07F9/24—Esteramides
- C07F9/2404—Esteramides the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/242—Esteramides the ester moiety containing a substituent or a structure which is considered as characteristic of hydroxyaryl compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL111697D NL111697C (enExample) | 1958-03-08 | ||
| DEF25209A DE1121882B (de) | 1958-03-08 | 1958-03-08 | Schaedlingsbekaempfungsmittel mit insektizider und akarizider Wirkung |
| CH7001259A CH383679A (de) | 1958-03-08 | 1959-02-24 | Schädlingsbekämpfungsmittel |
| FR788135A FR1221193A (fr) | 1958-03-08 | 1959-03-02 | Agents antiparasitaires |
| BE576263A BE576263A (fr) | 1958-03-08 | 1959-03-02 | Agents antiparasitaires |
| US797052A US2978479A (en) | 1958-03-08 | 1959-03-04 | Pest control agents |
| GB793859A GB880297A (en) | 1958-03-08 | 1959-03-06 | Phosphoric and thionophosphoric acid ester amides and diamides |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF25209A DE1121882B (de) | 1958-03-08 | 1958-03-08 | Schaedlingsbekaempfungsmittel mit insektizider und akarizider Wirkung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1121882B true DE1121882B (de) | 1962-01-11 |
Family
ID=7091532
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEF25209A Pending DE1121882B (de) | 1958-03-08 | 1958-03-08 | Schaedlingsbekaempfungsmittel mit insektizider und akarizider Wirkung |
Country Status (6)
| Country | Link |
|---|---|
| BE (1) | BE576263A (enExample) |
| CH (1) | CH383679A (enExample) |
| DE (1) | DE1121882B (enExample) |
| FR (1) | FR1221193A (enExample) |
| GB (1) | GB880297A (enExample) |
| NL (1) | NL111697C (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102007045955A1 (de) | 2007-09-26 | 2009-04-09 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| WO2010108616A1 (de) | 2009-03-25 | 2010-09-30 | Bayer Cropscience Ag | Nematizide, insektizide und akarizide wirkstoffkombinationen umfassend pyridylethylbenzamide und insektizide |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE790639A (fr) * | 1971-10-28 | 1973-04-27 | Bayer Ag | Chlorure de diester o-ethyl-o-(3-methyl-4- methylmercaptophenylique) d'acide phosphorique, son procede de preparation et son application commeproduit intermediaire pour la synthese de pesticides |
| BRPI0924451B1 (pt) | 2009-03-25 | 2017-12-26 | Bayer Intellectual Property Gmbh | Combinations of active substances and their uses, as well as methods for the control of animal pests and method for the manufacture of insecticides and acaricides |
-
0
- NL NL111697D patent/NL111697C/xx active
-
1958
- 1958-03-08 DE DEF25209A patent/DE1121882B/de active Pending
-
1959
- 1959-02-24 CH CH7001259A patent/CH383679A/de unknown
- 1959-03-02 FR FR788135A patent/FR1221193A/fr not_active Expired
- 1959-03-02 BE BE576263A patent/BE576263A/fr unknown
- 1959-03-06 GB GB793859A patent/GB880297A/en not_active Expired
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102007045955A1 (de) | 2007-09-26 | 2009-04-09 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| WO2010108616A1 (de) | 2009-03-25 | 2010-09-30 | Bayer Cropscience Ag | Nematizide, insektizide und akarizide wirkstoffkombinationen umfassend pyridylethylbenzamide und insektizide |
| EP2561758A1 (de) | 2009-03-25 | 2013-02-27 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und Thiodicarb |
| EP2561756A1 (de) | 2009-03-25 | 2013-02-27 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und Spirotetramat |
| EP2561757A1 (de) | 2009-03-25 | 2013-02-27 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und Ethiprole |
| EP2561755A1 (de) | 2009-03-25 | 2013-02-27 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und Mycorrhiza |
| EP2564704A1 (de) | 2009-03-25 | 2013-03-06 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und Methiocarb |
| EP2564698A1 (de) | 2009-03-25 | 2013-03-06 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und Bacillus firmus |
| EP2564701A1 (de) | 2009-03-25 | 2013-03-06 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und fluensulfone |
| EP2564699A1 (de) | 2009-03-25 | 2013-03-06 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und Metarhizium |
| EP2564700A1 (de) | 2009-03-25 | 2013-03-06 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und Hirsutella |
| EP2564705A1 (de) | 2009-03-25 | 2013-03-06 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und Pasteuria penetrans |
| EP2564703A1 (de) | 2009-03-25 | 2013-03-06 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und Rynaxypyr oder Cyazypyr |
| EP2564702A1 (de) | 2009-03-25 | 2013-03-06 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und ein weiterer Wirkstoff |
Also Published As
| Publication number | Publication date |
|---|---|
| CH383679A (de) | 1964-10-31 |
| GB880297A (en) | 1961-10-18 |
| FR1221193A (fr) | 1960-05-31 |
| BE576263A (fr) | 1959-07-01 |
| NL111697C (enExample) |
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