CH383678A - Nagetierbekämpfungsmittel - Google Patents
NagetierbekämpfungsmittelInfo
- Publication number
- CH383678A CH383678A CH6907559A CH6907559A CH383678A CH 383678 A CH383678 A CH 383678A CH 6907559 A CH6907559 A CH 6907559A CH 6907559 A CH6907559 A CH 6907559A CH 383678 A CH383678 A CH 383678A
- Authority
- CH
- Switzerland
- Prior art keywords
- acid
- ester
- grass
- dichlorodiphenyl
- acid esters
- Prior art date
Links
- 241000283984 Rodentia Species 0.000 title description 5
- 239000002253 acid Substances 0.000 claims description 11
- 239000004480 active ingredient Substances 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 11
- PTMHPRAIXMAOOB-UHFFFAOYSA-N phosphoramidic acid Chemical class NP(O)(O)=O PTMHPRAIXMAOOB-UHFFFAOYSA-N 0.000 claims description 10
- 241001465754 Metazoa Species 0.000 claims description 9
- 244000025254 Cannabis sativa Species 0.000 claims description 8
- 150000002148 esters Chemical class 0.000 claims description 8
- 239000003128 rodenticide Substances 0.000 claims description 8
- 241000699670 Mus sp. Species 0.000 claims description 6
- 206010011906 Death Diseases 0.000 claims description 3
- 241000699729 Muridae Species 0.000 claims description 3
- 238000002474 experimental method Methods 0.000 claims description 3
- 235000013305 food Nutrition 0.000 claims description 2
- 241000283973 Oryctolagus cuniculus Species 0.000 claims 3
- WZFUQSJFWNHZHM-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 WZFUQSJFWNHZHM-UHFFFAOYSA-N 0.000 claims 1
- 239000000839 emulsion Substances 0.000 claims 1
- 239000013589 supplement Substances 0.000 claims 1
- 241000700159 Rattus Species 0.000 description 8
- -1 phenyl ester Chemical class 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 241000196324 Embryophyta Species 0.000 description 4
- 241000238631 Hexapoda Species 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- 241000251468 Actinopterygii Species 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000001154 acute effect Effects 0.000 description 3
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 3
- 230000001186 cumulative effect Effects 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- 231100000419 toxicity Toxicity 0.000 description 3
- 230000001988 toxicity Effects 0.000 description 3
- 241001147360 Microtus agrestis Species 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 150000001993 dienes Chemical class 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 231100000614 poison Toxicity 0.000 description 2
- 239000011814 protection agent Substances 0.000 description 2
- WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 description 1
- 241001124076 Aphididae Species 0.000 description 1
- 241000254173 Coleoptera Species 0.000 description 1
- 241000255925 Diptera Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229910017974 NH40H Inorganic materials 0.000 description 1
- 241000131102 Oryzaephilus Species 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 230000006750 UV protection Effects 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 231100000460 acute oral toxicity Toxicity 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 230000009435 amidation Effects 0.000 description 1
- 238000007112 amidation reaction Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000001684 chronic effect Effects 0.000 description 1
- NBAUUSKPFGFBQZ-UHFFFAOYSA-N diethylaminophosphonic acid Chemical compound CCN(CC)P(O)(O)=O NBAUUSKPFGFBQZ-UHFFFAOYSA-N 0.000 description 1
- YNHXBEVSSILHPI-UHFFFAOYSA-N dimethylamidophosphoric dichloride Chemical compound CN(C)P(Cl)(Cl)=O YNHXBEVSSILHPI-UHFFFAOYSA-N 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000004459 forage Substances 0.000 description 1
- 230000035929 gnawing Effects 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 150000003017 phosphorus Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- KPHOBSTVDZCCAU-UHFFFAOYSA-N tetracyclo[6.4.0.02,4.05,7]dodeca-1(12),2(4),5(7),8,10-pentaene Chemical compound C1=CC=CC2=C3CC3=C(C3)C3=C21 KPHOBSTVDZCCAU-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 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
-
- 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
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/576—Six-membered rings
- C07F9/59—Hydrogenated pyridine rings
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)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF25085A DE1076437B (de) | 1958-02-20 | 1958-02-20 | Nagetierbekaempfungsmittel |
Publications (1)
Publication Number | Publication Date |
---|---|
CH383678A true CH383678A (de) | 1964-10-31 |
Family
ID=7091480
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH6907559A CH383678A (de) | 1958-02-20 | 1959-02-03 | Nagetierbekämpfungsmittel |
Country Status (7)
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE554888A (US08088918-20120103-C00476.png) * | 1956-12-20 | |||
BE583244A (US08088918-20120103-C00476.png) * | 1958-10-03 | |||
US3162666A (en) * | 1962-07-09 | 1964-12-22 | Dow Chemical Co | Omicron-aryl s-aryl phosphoramidodithioates |
DE1196897B (de) * | 1962-08-23 | 1965-07-15 | Bayer Ag | Rodentizide Mittel |
US3207661A (en) * | 1963-01-11 | 1965-09-21 | American Agricultural Chem Co | Bis-(aziridinyl)-phosphinothioic esters as chemical sterilants for insects and mites |
US3282847A (en) * | 1965-07-28 | 1966-11-01 | Bayer Ag | Hydraulic fluids |
CH521717A (de) * | 1968-12-10 | 1972-04-30 | Bayer Ag | Verwendung von Phosphor- oder Phosphon- bzw. Thionophosphor- oder Thionophosphonsäureestern zur Bekämpfung von Nagetieren und Hasenartigen |
US3937765A (en) * | 1970-10-12 | 1976-02-10 | Stauffer Chemical Company | Process for preparing 0,0-diaryl n,n-dialkyl phosphoramidates |
US3923733A (en) * | 1973-04-13 | 1975-12-02 | American Cyanamid Co | Polyolefin light stabilizers |
US3984348A (en) * | 1973-11-05 | 1976-10-05 | American Cyanamid Company | Polyolefin light stabilizers |
CA2576530A1 (en) * | 2004-08-11 | 2006-02-23 | Donald L. Barbeau | Noncardiotoxic pharmaceutical compounds |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2146356A (en) * | 1935-07-02 | 1939-02-07 | Winthrop Chem Co Inc | Dialkylaminophosphorous fluorides and a process for preparing the same |
DE767723C (de) * | 1937-02-03 | 1953-04-09 | Bayer Ag | Schaedlingsbekaempfungsmittel |
DE767930C (de) * | 1938-08-04 | 1955-01-10 | Bayer Ag | Schaedlingsbekaempfungsmittel |
NL67747C (US08088918-20120103-C00476.png) * | 1947-12-26 | |||
CA494562A (en) * | 1948-02-04 | 1953-07-21 | American Cyanamid Company | Carbamylalkyl phosphates and method of preparation |
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 |
US2494284A (en) * | 1949-01-12 | 1950-01-10 | American Cyanamid Co | Cyanoalkyl phosphates and method of preparation |
CH355775A (de) * | 1956-04-21 | 1961-07-31 | Bayer Ag | Verfahren zur Herstellung von Thiophosphorsäureestern |
-
0
- BE BE575869D patent/BE575869A/xx unknown
- NL NL236264D patent/NL236264A/xx unknown
-
1958
- 1958-02-20 DE DEF25085A patent/DE1076437B/de active Pending
-
1959
- 1959-02-03 CH CH6907559A patent/CH383678A/de unknown
- 1959-02-13 GB GB5138/59A patent/GB844037A/en not_active Expired
- 1959-02-17 US US793697A patent/US2994638A/en not_active Expired - Lifetime
- 1959-02-19 FR FR787134A patent/FR1217380A/fr not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR1217380A (fr) | 1960-05-03 |
US2994638A (en) | 1961-08-01 |
GB844037A (en) | 1960-08-10 |
DE1076437B (de) | 1960-02-25 |
NL236264A (US08088918-20120103-C00476.png) | 1900-01-01 |
BE575869A (US08088918-20120103-C00476.png) | 1900-01-01 |
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