DE2223677A1 - Insecticide - Google Patents
InsecticideInfo
- Publication number
- DE2223677A1 DE2223677A1 DE19722223677 DE2223677A DE2223677A1 DE 2223677 A1 DE2223677 A1 DE 2223677A1 DE 19722223677 DE19722223677 DE 19722223677 DE 2223677 A DE2223677 A DE 2223677A DE 2223677 A1 DE2223677 A1 DE 2223677A1
- Authority
- DE
- Germany
- Prior art keywords
- ddt
- insecticide
- chlorinated hydrocarbons
- insecticides
- enzymes
- 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
- 239000002917 insecticide Substances 0.000 title claims description 22
- 102000004190 Enzymes Human genes 0.000 claims description 10
- 108090000790 Enzymes Proteins 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 5
- 230000002503 metabolic effect Effects 0.000 claims description 4
- 150000001555 benzenes Chemical class 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- HFFLGKNGCAIQMO-UHFFFAOYSA-N trichloroacetaldehyde Chemical compound ClC(Cl)(Cl)C=O HFFLGKNGCAIQMO-UHFFFAOYSA-N 0.000 claims description 2
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 claims 3
- 238000009472 formulation Methods 0.000 claims 1
- YVGGHNCTFXOJCH-UHFFFAOYSA-N DDT Chemical compound C1=CC(Cl)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(Cl)C=C1 YVGGHNCTFXOJCH-UHFFFAOYSA-N 0.000 description 33
- 150000001875 compounds Chemical class 0.000 description 10
- 230000000749 insecticidal effect Effects 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 241000124008 Mammalia Species 0.000 description 8
- 241001465754 Metazoa Species 0.000 description 8
- 235000013305 food Nutrition 0.000 description 8
- IAKOZHOLGAGEJT-UHFFFAOYSA-N 1,1,1-trichloro-2,2-bis(p-methoxyphenyl)-Ethane Chemical compound C1=CC(OC)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(OC)C=C1 IAKOZHOLGAGEJT-UHFFFAOYSA-N 0.000 description 7
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- 241000238631 Hexapoda Species 0.000 description 6
- 231100000419 toxicity Toxicity 0.000 description 6
- 230000001988 toxicity Effects 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 241000255925 Diptera Species 0.000 description 4
- 241000699670 Mus sp. Species 0.000 description 4
- 241000251468 Actinopterygii Species 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 241000257159 Musca domestica Species 0.000 description 3
- 241000257226 Muscidae Species 0.000 description 3
- 241000209072 Sorghum Species 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000009825 accumulation Methods 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 231100000053 low toxicity Toxicity 0.000 description 3
- -1 methylchlor, 1,1,1-trichloro-2,2-bis (p-methylphenyl) ethane Chemical compound 0.000 description 3
- 230000002085 persistent effect Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- HNKJADCVZUBCPG-UHFFFAOYSA-N thioanisole Chemical compound CSC1=CC=CC=C1 HNKJADCVZUBCPG-UHFFFAOYSA-N 0.000 description 3
- LBWJWHHOEQICIL-UHFFFAOYSA-N 1-methylsulfanyl-4-[2,2,2-trichloro-1-(4-methylsulfanylphenyl)ethyl]benzene Chemical compound C1=CC(SC)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(SC)C=C1 LBWJWHHOEQICIL-UHFFFAOYSA-N 0.000 description 2
- 241000195493 Cryptophyta Species 0.000 description 2
- 241000256057 Culex quinquefasciatus Species 0.000 description 2
- 241000256113 Culicidae Species 0.000 description 2
- AHJKRLASYNVKDZ-UHFFFAOYSA-N DDD Chemical compound C=1C=C(Cl)C=CC=1C(C(Cl)Cl)C1=CC=C(Cl)C=C1 AHJKRLASYNVKDZ-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 102000004316 Oxidoreductases Human genes 0.000 description 2
- 108090000854 Oxidoreductases Proteins 0.000 description 2
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000001784 detoxification Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000000361 pesticidal effect Effects 0.000 description 2
- 239000000575 pesticide Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- YHDIGZDVODUGOD-UHFFFAOYSA-N 1-methoxy-4-[2,2,2-trichloro-1-(4-methylsulfanylphenyl)ethyl]benzene Chemical compound C1=CC(OC)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(SC)C=C1 YHDIGZDVODUGOD-UHFFFAOYSA-N 0.000 description 1
- DQMIPRIVNVYSDB-UHFFFAOYSA-N 2,2,2-trichloro-1-(4-methoxyphenyl)ethanol Chemical compound COC1=CC=C(C(O)C(Cl)(Cl)Cl)C=C1 DQMIPRIVNVYSDB-UHFFFAOYSA-N 0.000 description 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 1
- 206010002091 Anaesthesia Diseases 0.000 description 1
- 241000256186 Anopheles <genus> Species 0.000 description 1
- 241000256187 Anopheles albimanus Species 0.000 description 1
- 241000271566 Aves Species 0.000 description 1
- SNIMHCBJFOYKIK-UHFFFAOYSA-N CO[ClH]C(C(Cl)(Cl)Cl)(C1=CC=C(C=C1)OC)C1=CC=C(C=C1)OC Chemical compound CO[ClH]C(C(Cl)(Cl)Cl)(C1=CC=C(C=C1)OC)C1=CC=C(C=C1)OC SNIMHCBJFOYKIK-UHFFFAOYSA-N 0.000 description 1
- 241000256054 Culex <genus> Species 0.000 description 1
- 241000238578 Daphnia Species 0.000 description 1
- 241000567412 Estigmene acrea Species 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 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
- 241000237858 Gastropoda Species 0.000 description 1
- 241001562042 Physa Species 0.000 description 1
- 239000006004 Quartz sand Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 241000251539 Vertebrata <Metazoa> Species 0.000 description 1
- 150000005224 alkoxybenzenes Chemical class 0.000 description 1
- 230000037005 anaesthesia Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000007857 degradation product Substances 0.000 description 1
- 238000007033 dehydrochlorination reaction Methods 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000000378 dietary effect Effects 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 231100000566 intoxication Toxicity 0.000 description 1
- 230000035987 intoxication Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229960004793 sucrose Drugs 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C25/00—Compounds containing at least one halogen atom bound to a six-membered aromatic ring
- C07C25/18—Polycyclic aromatic halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US14724771A | 1971-05-26 | 1971-05-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2223677A1 true DE2223677A1 (de) | 1972-12-07 |
Family
ID=22520828
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19722223677 Pending DE2223677A1 (de) | 1971-05-26 | 1972-05-16 | Insecticide |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US3787505A (enExample) |
| AR (1) | AR193096A1 (enExample) |
| AU (1) | AU469957B2 (enExample) |
| BE (1) | BE784066A (enExample) |
| BR (1) | BR7203286D0 (enExample) |
| CA (1) | CA1024534A (enExample) |
| CH (1) | CH570349A5 (enExample) |
| DE (1) | DE2223677A1 (enExample) |
| ES (1) | ES403185A1 (enExample) |
| FR (1) | FR2139018A1 (enExample) |
| GB (1) | GB1397797A (enExample) |
| IL (1) | IL39508A (enExample) |
| IT (1) | IT958980B (enExample) |
| NL (1) | NL7207155A (enExample) |
| PH (1) | PH10637A (enExample) |
| ZA (1) | ZA723397B (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3939277A (en) * | 1971-05-26 | 1976-02-17 | The University Of Illinois Foundation | Insecticidal biodegradable analogues of DDT |
| US3855313A (en) * | 1971-05-26 | 1974-12-17 | Univ Illinois | Insecticidal biodegradable methylthio analogs of ddt |
| US3966824A (en) * | 1972-12-26 | 1976-06-29 | University Of Illinois Foundation | P,P'-Disubstituted α-trichloromethylbenzylphenyl ethers |
| US3932527A (en) * | 1973-11-19 | 1976-01-13 | University Of Illinois Foundation | Preparation of p-p-disubstituted diaryl trichloroethanes |
| NL7500478A (nl) * | 1974-01-21 | 1975-07-23 | Ciba Geigy | Werkwijze voor het bereiden van nieuwe difenylverbindingen. |
-
1971
- 1971-05-26 US US00147247A patent/US3787505A/en not_active Expired - Lifetime
-
1972
- 1972-05-09 CA CA141,724A patent/CA1024534A/en not_active Expired
- 1972-05-11 AU AU42151/72A patent/AU469957B2/en not_active Expired
- 1972-05-16 DE DE19722223677 patent/DE2223677A1/de active Pending
- 1972-05-18 ZA ZA723397A patent/ZA723397B/xx unknown
- 1972-05-19 GB GB2358872A patent/GB1397797A/en not_active Expired
- 1972-05-23 IL IL39508A patent/IL39508A/en unknown
- 1972-05-24 BR BR3286/72A patent/BR7203286D0/pt unknown
- 1972-05-25 ES ES403185A patent/ES403185A1/es not_active Expired
- 1972-05-25 FR FR7218642A patent/FR2139018A1/fr not_active Withdrawn
- 1972-05-25 IT IT68670/72A patent/IT958980B/it active
- 1972-05-26 CH CH783972A patent/CH570349A5/xx not_active IP Right Cessation
- 1972-05-26 NL NL7207155A patent/NL7207155A/xx unknown
- 1972-05-26 PH PH13575A patent/PH10637A/en unknown
- 1972-05-26 BE BE784066A patent/BE784066A/xx unknown
- 1972-06-08 AR AR242441A patent/AR193096A1/es active
Also Published As
| Publication number | Publication date |
|---|---|
| GB1397797A (en) | 1975-06-18 |
| US3787505A (en) | 1974-01-22 |
| IL39508A0 (en) | 1972-07-26 |
| FR2139018A1 (enExample) | 1973-01-05 |
| ES403185A1 (es) | 1976-03-01 |
| PH10637A (en) | 1977-07-21 |
| AR193096A1 (es) | 1973-03-30 |
| IL39508A (en) | 1976-04-30 |
| BE784066A (fr) | 1972-09-18 |
| AU4215172A (en) | 1973-11-15 |
| CH570349A5 (enExample) | 1975-12-15 |
| CA1024534A (en) | 1978-01-17 |
| NL7207155A (enExample) | 1972-11-28 |
| AU469957B2 (en) | 1976-02-26 |
| BR7203286D0 (pt) | 1974-08-15 |
| ZA723397B (en) | 1973-02-28 |
| IT958980B (it) | 1973-10-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OHJ | Non-payment of the annual fee |