DE1116468B - Akarizide mit ovizider Wirkung - Google Patents
Akarizide mit ovizider WirkungInfo
- Publication number
- DE1116468B DE1116468B DEF26718A DEF0026718A DE1116468B DE 1116468 B DE1116468 B DE 1116468B DE F26718 A DEF26718 A DE F26718A DE F0026718 A DEF0026718 A DE F0026718A DE 1116468 B DE1116468 B DE 1116468B
- Authority
- DE
- Germany
- Prior art keywords
- radical
- acaricides
- hydrogen
- active ingredient
- chlorine
- 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
- 230000003151 ovacidal effect Effects 0.000 title claims description 7
- 230000000895 acaricidal effect Effects 0.000 title claims description 5
- 239000000642 acaricide Substances 0.000 title claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 2
- 125000005842 heteroatom Chemical group 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 239000004606 Fillers/Extenders Substances 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 11
- 241001454295 Tetranychidae Species 0.000 description 6
- 235000013601 eggs Nutrition 0.000 description 6
- -1 Amidophosphoric acid diaryl ester Chemical class 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- PTMHPRAIXMAOOB-UHFFFAOYSA-N phosphoramidic acid Chemical compound NP(O)(O)=O PTMHPRAIXMAOOB-UHFFFAOYSA-N 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 241001454293 Tetranychus urticae Species 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 239000000575 pesticide Substances 0.000 description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- 244000046052 Phaseolus vulgaris Species 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- 230000000749 insecticidal effect Effects 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 231100000194 ovacidal Toxicity 0.000 description 2
- 150000003014 phosphoric acid esters Chemical class 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- 239000011814 protection agent Substances 0.000 description 2
- 150000003580 thiophosphoric acid esters Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- BBAMTDMNXVSCRU-UHFFFAOYSA-N (4-chlorophenyl) dihydrogen phosphate Chemical class OP(O)(=O)OC1=CC=C(Cl)C=C1 BBAMTDMNXVSCRU-UHFFFAOYSA-N 0.000 description 1
- ZQDPJFUHLCOCRG-UHFFFAOYSA-N 3-hexene Chemical group CCC=CCC ZQDPJFUHLCOCRG-UHFFFAOYSA-N 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- 206010061217 Infestation Diseases 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- YUWBVKYVJWNVLE-UHFFFAOYSA-N [N].[P] Chemical class [N].[P] YUWBVKYVJWNVLE-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000004104 aryloxy group Chemical group 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
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000006378 damage Effects 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
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 125000004437 phosphorous atom Chemical group 0.000 description 1
- 125000003386 piperidinyl group Chemical group 0.000 description 1
- 239000004476 plant protection product Substances 0.000 description 1
- 230000001119 rodenticidal effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000008096 xylene Substances 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
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6527—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and oxygen atoms as the only ring hetero atoms
- C07F9/6533—Six-membered rings
-
- 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
-
- 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
-
- 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
- C07F9/2454—Esteramides the amide moiety containing a substituent or a structure which is considered as characteristic
- C07F9/2458—Esteramides the amide moiety containing a substituent or a structure which is considered as characteristic of aliphatic amines
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 (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE583244D BE583244A (US08088918-20120103-C00131.png) | 1958-10-03 | ||
| NL243963D NL243963A (US08088918-20120103-C00131.png) | 1958-10-03 | ||
| DEF26718A DE1116468B (de) | 1958-10-03 | 1958-10-03 | Akarizide mit ovizider Wirkung |
| CH7798059A CH389317A (de) | 1958-10-03 | 1959-09-08 | Akarizides und ovizides Pflanzenschutzmittel |
| US840253A US3058879A (en) | 1958-10-03 | 1959-09-16 | Acaricidal and ovicidal agents |
| FR806520A FR1244501A (fr) | 1958-10-03 | 1959-10-01 | Produit pour la destruction des acariens et de leurs oeufs |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF26718A DE1116468B (de) | 1958-10-03 | 1958-10-03 | Akarizide mit ovizider Wirkung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1116468B true DE1116468B (de) | 1961-11-02 |
Family
ID=7092131
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEF26718A Pending DE1116468B (de) | 1958-10-03 | 1958-10-03 | Akarizide mit ovizider Wirkung |
Country Status (6)
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102926202A (zh) * | 2012-09-25 | 2013-02-13 | 台州学院 | 一种阻燃涂层及其制备方法和应用 |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6596291B2 (en) | 1997-12-05 | 2003-07-22 | Thomas A. Bell | Compositions and methods for treating surfaces infected with ectoparasitic insects |
| US8088918B2 (en) * | 2004-08-11 | 2012-01-03 | Williamsburg Holdings Llc | Noncardiotoxic pharmaceutical compounds |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH201549A (de) * | 1937-09-06 | 1938-12-15 | Geigy Ag J R | Verfahren zum Bekämpfen von Insekten, deren Larven und andern Schädlingen. |
| GB655875A (en) * | 1947-03-15 | 1951-08-08 | American Cyanamid Co | Improvements in or relating to pesticidal compositions |
| DE811514C (de) * | 1948-10-06 | 1951-08-20 | Bayer Ag | Schaedlingsbekaempfungsmittel |
| US2615037A (en) * | 1948-10-15 | 1952-10-21 | Dow Chemical Co | O,o-di(4-chlorophenyl) n-alkylamidothiophosphates |
| US2615039A (en) * | 1949-11-02 | 1952-10-21 | Dow Chemical Co | Amidothiophosphates |
| US2615038A (en) * | 1948-10-15 | 1952-10-21 | Dow Chemical Co | O,o-di(polyhalophenyl) n-substituted amidothiophosphates |
| DE941459C (de) * | 1949-06-09 | 1956-04-12 | Dow Chemical Co | Bekaempfung von Insekten und Pilzen |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2635112A (en) * | 1949-07-28 | 1953-04-14 | Research Corp | Process for producing aminomethylphosphonic acid compounds |
| NL93954C (US08088918-20120103-C00131.png) * | 1955-03-21 | 1900-01-01 | ||
| NL101816C (US08088918-20120103-C00131.png) * | 1955-05-03 | |||
| US2802823A (en) * | 1956-04-30 | 1957-08-13 | Dow Chemical Co | Omicron-(chlorophenyl) omicron-lower alkyl phosphoroamidothioates |
| NL236264A (US08088918-20120103-C00131.png) * | 1958-02-20 | 1900-01-01 |
-
0
- NL NL243963D patent/NL243963A/xx unknown
- BE BE583244D patent/BE583244A/xx unknown
-
1958
- 1958-10-03 DE DEF26718A patent/DE1116468B/de active Pending
-
1959
- 1959-09-08 CH CH7798059A patent/CH389317A/de unknown
- 1959-09-16 US US840253A patent/US3058879A/en not_active Expired - Lifetime
- 1959-10-01 FR FR806520A patent/FR1244501A/fr not_active Expired
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH201549A (de) * | 1937-09-06 | 1938-12-15 | Geigy Ag J R | Verfahren zum Bekämpfen von Insekten, deren Larven und andern Schädlingen. |
| GB655875A (en) * | 1947-03-15 | 1951-08-08 | American Cyanamid Co | Improvements in or relating to pesticidal compositions |
| DE811514C (de) * | 1948-10-06 | 1951-08-20 | Bayer Ag | Schaedlingsbekaempfungsmittel |
| US2615037A (en) * | 1948-10-15 | 1952-10-21 | Dow Chemical Co | O,o-di(4-chlorophenyl) n-alkylamidothiophosphates |
| US2615038A (en) * | 1948-10-15 | 1952-10-21 | Dow Chemical Co | O,o-di(polyhalophenyl) n-substituted amidothiophosphates |
| DE941459C (de) * | 1949-06-09 | 1956-04-12 | Dow Chemical Co | Bekaempfung von Insekten und Pilzen |
| US2615039A (en) * | 1949-11-02 | 1952-10-21 | Dow Chemical Co | Amidothiophosphates |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102926202A (zh) * | 2012-09-25 | 2013-02-13 | 台州学院 | 一种阻燃涂层及其制备方法和应用 |
Also Published As
| Publication number | Publication date |
|---|---|
| BE583244A (US08088918-20120103-C00131.png) | |
| NL243963A (US08088918-20120103-C00131.png) | |
| CH389317A (de) | 1965-03-15 |
| US3058879A (en) | 1962-10-16 |
| FR1244501A (fr) | 1960-10-28 |
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