PL94420B1 - Srodek owadobojczy - Google Patents
Srodek owadobojczy Download PDFInfo
- Publication number
- PL94420B1 PL94420B1 PL1974174918A PL17491874A PL94420B1 PL 94420 B1 PL94420 B1 PL 94420B1 PL 1974174918 A PL1974174918 A PL 1974174918A PL 17491874 A PL17491874 A PL 17491874A PL 94420 B1 PL94420 B1 PL 94420B1
- Authority
- PL
- Poland
- Prior art keywords
- compound
- trans
- parts
- phenoxybenzyl
- ratio
- Prior art date
Links
- 239000002917 insecticide Substances 0.000 title claims description 13
- 239000002253 acid Substances 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 7
- 235000007516 Chrysanthemum Nutrition 0.000 claims description 6
- 150000002148 esters Chemical class 0.000 claims description 6
- -1 3-phenoxybenzyl Chemical group 0.000 claims description 5
- YMGUBTXCNDTFJI-UHFFFAOYSA-M cyclopropanecarboxylate Chemical compound [O-]C(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-M 0.000 claims description 5
- 239000013543 active substance Substances 0.000 claims description 3
- XLOPRKKSAJMMEW-SFYZADRCSA-N Chrysanthemic acid Natural products CC(C)=C[C@@H]1[C@@H](C(O)=O)C1(C)C XLOPRKKSAJMMEW-SFYZADRCSA-N 0.000 claims 2
- XLOPRKKSAJMMEW-UHFFFAOYSA-N chrysanthemic acid Chemical compound CC(C)=CC1C(C(O)=O)C1(C)C XLOPRKKSAJMMEW-UHFFFAOYSA-N 0.000 claims 2
- 244000189548 Chrysanthemum x morifolium Species 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 33
- 241000255925 Diptera Species 0.000 description 23
- 150000001875 compounds Chemical class 0.000 description 18
- 229940125904 compound 1 Drugs 0.000 description 17
- 238000002360 preparation method Methods 0.000 description 17
- 229940125782 compound 2 Drugs 0.000 description 15
- 241000238631 Hexapoda Species 0.000 description 11
- 238000009472 formulation Methods 0.000 description 8
- 230000000749 insecticidal effect Effects 0.000 description 8
- 239000000443 aerosol Substances 0.000 description 7
- 239000012141 concentrate Substances 0.000 description 7
- 239000000839 emulsion Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- 239000011521 glass Substances 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 241000723353 Chrysanthemum Species 0.000 description 5
- 240000007594 Oryza sativa Species 0.000 description 5
- 241000607479 Yersinia pestis Species 0.000 description 5
- 239000003350 kerosene Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 241000196324 Embryophyta Species 0.000 description 4
- 230000002195 synergetic effect Effects 0.000 description 4
- 241000238876 Acari Species 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 235000013339 cereals Nutrition 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000004570 mortar (masonry) Substances 0.000 description 3
- 239000011120 plywood Substances 0.000 description 3
- 238000009331 sowing Methods 0.000 description 3
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 2
- 241001674044 Blattodea Species 0.000 description 2
- 240000007124 Brassica oleracea Species 0.000 description 2
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 description 2
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 2
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 2
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 2
- 239000004322 Butylated hydroxytoluene Substances 0.000 description 2
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 240000001307 Myosotis scorpioides Species 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 2
- 229940095259 butylated hydroxytoluene Drugs 0.000 description 2
- 229940126214 compound 3 Drugs 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 229960005235 piperonyl butoxide Drugs 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 239000004563 wettable powder Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- 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 1
- GNEPLYVYORHREW-UHFFFAOYSA-N 1,1,3,3,6-pentamethyl-7-nitro-2h-inden-5-amine Chemical compound CC1=C(N)C=C2C(C)(C)CC(C)(C)C2=C1[N+]([O-])=O GNEPLYVYORHREW-UHFFFAOYSA-N 0.000 description 1
- CSXOGACWYJFTLV-UHFFFAOYSA-N 4-methyl-5-propyl-1,3-benzodioxole Chemical compound CCCC1=CC=C2OCOC2=C1C CSXOGACWYJFTLV-UHFFFAOYSA-N 0.000 description 1
- 241000157282 Aesculus Species 0.000 description 1
- 241001124076 Aphididae Species 0.000 description 1
- 241000239290 Araneae Species 0.000 description 1
- 241000238657 Blattella germanica Species 0.000 description 1
- 235000010149 Brassica rapa subsp chinensis Nutrition 0.000 description 1
- 235000000536 Brassica rapa subsp pekinensis Nutrition 0.000 description 1
- 241000499436 Brassica rapa subsp. pekinensis Species 0.000 description 1
- 239000004255 Butylated hydroxyanisole Substances 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- 241000270722 Crocodylidae Species 0.000 description 1
- 241000256113 Culicidae Species 0.000 description 1
- 206010014405 Electrocution Diseases 0.000 description 1
- 206010061217 Infestation Diseases 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 241001674048 Phthiraptera Species 0.000 description 1
- 241000255969 Pieris brassicae Species 0.000 description 1
- 241000500437 Plutella xylostella Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 241001415849 Strigiformes Species 0.000 description 1
- 240000004460 Tanacetum coccineum Species 0.000 description 1
- CVQODEWAPZVVBU-UHFFFAOYSA-N XMC Chemical compound CNC(=O)OC1=CC(C)=CC(C)=C1 CVQODEWAPZVVBU-UHFFFAOYSA-N 0.000 description 1
- ROVGZAWFACYCSP-MQBLHHJJSA-N [2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(C\C=C/C=C)C(=O)C1 ROVGZAWFACYCSP-MQBLHHJJSA-N 0.000 description 1
- ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 230000000845 anti-microbial effect Effects 0.000 description 1
- 230000001442 anti-mosquito Effects 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 210000001142 back Anatomy 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 235000019282 butylated hydroxyanisole Nutrition 0.000 description 1
- CZBZUDVBLSSABA-UHFFFAOYSA-N butylated hydroxyanisole Chemical compound COC1=CC=C(O)C(C(C)(C)C)=C1.COC1=CC=C(O)C=C1C(C)(C)C CZBZUDVBLSSABA-UHFFFAOYSA-N 0.000 description 1
- 229940043253 butylated hydroxyanisole Drugs 0.000 description 1
- CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 description 1
- 235000012730 carminic acid Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 210000001520 comb Anatomy 0.000 description 1
- SCKHCCSZFPSHGR-UHFFFAOYSA-N cyanophos Chemical compound COP(=S)(OC)OC1=CC=C(C#N)C=C1 SCKHCCSZFPSHGR-UHFFFAOYSA-N 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 235000021186 dishes Nutrition 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000005003 food packaging material Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 235000010181 horse chestnut Nutrition 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000000201 insect hormone Substances 0.000 description 1
- 239000003915 liquefied petroleum gas Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- WLLGXSLBOPFWQV-OTHKPKEBSA-N molport-035-783-878 Chemical compound C([C@H]1C=C2)[C@H]2C2C1C(=O)N(CC(CC)CCCC)C2=O WLLGXSLBOPFWQV-OTHKPKEBSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- SGSDSJVQCWBUAO-UHFFFAOYSA-N n-phenoxynaphthalen-1-amine Chemical class C=1C=CC2=CC=CC=C2C=1NOC1=CC=CC=C1 SGSDSJVQCWBUAO-UHFFFAOYSA-N 0.000 description 1
- 230000001338 necrotic effect Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000012794 pre-harvesting Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 1
- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 description 1
- 229940015367 pyrethrum Drugs 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 239000012747 synergistic agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
- 210000001685 thyroid gland Anatomy 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
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 |
|---|---|---|---|
| JP11749773A JPS5710842B2 (en, 2012) | 1973-10-18 | 1973-10-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL94420B1 true PL94420B1 (pl) | 1977-08-31 |
Family
ID=14713185
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL1974174918A PL94420B1 (pl) | 1973-10-18 | 1974-10-18 | Srodek owadobojczy |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US3899586A (en, 2012) |
| JP (1) | JPS5710842B2 (en, 2012) |
| AR (1) | AR224323A1 (en, 2012) |
| AU (1) | AU467738B2 (en, 2012) |
| BE (1) | BE872872Q (en, 2012) |
| CA (1) | CA1031256A (en, 2012) |
| CH (1) | CH604515A5 (en, 2012) |
| CS (1) | CS180027B2 (en, 2012) |
| CY (1) | CY1024A (en, 2012) |
| DE (1) | DE2449546C2 (en, 2012) |
| DK (1) | DK136343B (en, 2012) |
| DO (1) | DOP1979002750A (en, 2012) |
| ES (1) | ES431108A1 (en, 2012) |
| FR (1) | FR2247974B1 (en, 2012) |
| GB (1) | GB1447193A (en, 2012) |
| HK (1) | HK33079A (en, 2012) |
| IT (1) | IT1050252B (en, 2012) |
| KE (1) | KE2995A (en, 2012) |
| MY (1) | MY7900176A (en, 2012) |
| NL (1) | NL161655C (en, 2012) |
| PL (1) | PL94420B1 (en, 2012) |
| SU (1) | SU631051A3 (en, 2012) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1590577A (en) * | 1976-09-06 | 1981-06-03 | Ici Ltd | Insecticidal compositions |
| ZA785688B (en) * | 1977-10-11 | 1980-05-28 | Wellcome Found | Pesticidal compositions |
| US4357350A (en) * | 1978-05-17 | 1982-11-02 | Roussel Uclaf | Novel acaricide compositions |
| FR2426673A1 (fr) * | 1978-05-25 | 1979-12-21 | Nat Res Dev | Pesticides du type pyrethrine |
| AU528416B2 (en) * | 1978-05-30 | 1983-04-28 | Wellcome Foundation Limited, The | Pesticidal formulations |
| JPS5527104A (en) * | 1978-07-19 | 1980-02-27 | Sumitomo Chem Co Ltd | Pesticidal composition |
| FR2500265A1 (fr) * | 1981-02-20 | 1982-08-27 | Roussel Uclaf | Compositions pesticides contenant un melange synergique de 1r, cis 2,2-dimethyl 3(2,2-dihalovinyl) cyclopropane-1-carboxylate de (s) a-cyano 3-phenoxybenzyle et d'autres composes pyrethrinoides |
| GB2098480B (en) * | 1981-04-27 | 1984-09-19 | Ici Plc | Insecticidal compositions |
| US5925368A (en) * | 1981-10-26 | 1999-07-20 | Battelle Memorial Institute | Protection of wooden objects in direct contact with soil from pest invasion |
| US6331308B1 (en) | 1981-10-26 | 2001-12-18 | Battelle Memorial Institute | Method and apparatus for providing long term protection from intrusion by insects and other cold blooded animals |
| US6099850A (en) * | 1981-10-26 | 2000-08-08 | Battelle Memorial Institute | Termite and boring insect barrier for the protection of wooden structures |
| US6060076A (en) * | 1981-10-26 | 2000-05-09 | Battelle Memorial Institute | Method and apparatus for providing long term protection from intrusion by insects and other cold blooded animals |
| JPS59176711A (ja) * | 1983-03-25 | 1984-10-06 | Matsushita Electric Ind Co Ltd | レンズ移動装置 |
| JPS59227806A (ja) * | 1983-06-10 | 1984-12-21 | Sumitomo Chem Co Ltd | 殺虫組成物 |
| FR2599220A1 (fr) * | 1986-05-29 | 1987-12-04 | Aerosols Ste Mediterraneenne | Nouvelle composition parasiticide a effet prolonge pour la prevention ou le traitement externe de l'homme et des animaux a sang chaud. |
| US6572872B2 (en) | 1989-09-01 | 2003-06-03 | Battelle Memorial Institute | Method and apparatus for providing long term protection from intrusion by insects and other cold blooded animals |
| US6852328B1 (en) | 1989-09-01 | 2005-02-08 | Battelle Memorial Institute K1-53 | Method and device for protection of wooden objects proximate soil from pest invasion |
| US6319511B1 (en) | 1989-09-01 | 2001-11-20 | Battelle Memorial Institute | Termite and boring insect barrier for the protection of wooden structures |
| JP3052142B2 (ja) * | 1989-09-14 | 2000-06-12 | 住友化学工業株式会社 | 殺虫、殺ダニ組成物 |
| JPH0734699B2 (ja) * | 1991-03-14 | 1995-04-19 | アース製薬株式会社 | 屋内ダニ防除用エアゾール剤およびそれを用いた屋内ダニ防除方法 |
| US5856271A (en) * | 1995-06-07 | 1999-01-05 | Battelle Memorial Institute | Method of making controlled released devices |
| JPH10236905A (ja) * | 1997-02-25 | 1998-09-08 | Sumitomo Chem Co Ltd | 衣料害虫防除剤 |
| US5985304A (en) | 1998-02-25 | 1999-11-16 | Battelle Memorial Institute | Barrier preventing wood pest access to wooden structures |
| RU2134509C1 (ru) * | 1998-03-16 | 1999-08-20 | Закрытое акционерное общество "Экспериментально-производственный центр "Дезинфекционист" | Инсектицидный состав "рибор-нео" |
| FR2811202B1 (fr) * | 2000-07-06 | 2004-04-09 | Prod Berger | Procede de diffusion d'une composition acaricide comprenant de la permethrine et de la tetramethrine et utilisation d'un flacon a combustion catalytique pour la mise en oeuvre d'un tel procede |
| ITMI20020287A1 (it) * | 2002-02-14 | 2003-08-14 | Endura Spa | Derevati del benzodiossolo come modulatori dell'attivita' proteolitica in piante e nei loro parassiti |
| BR122015017095B1 (pt) * | 2005-12-22 | 2016-05-10 | Fmc Corp | composição inseticida compreendendo bifentrina |
| JP2009062299A (ja) * | 2007-09-05 | 2009-03-26 | Sumitomo Chemical Co Ltd | 有害生物防除組成物及び有害生物の防除方法 |
| JP5365403B2 (ja) * | 2009-07-31 | 2013-12-11 | 住友化学株式会社 | 害虫防除用組成物及び害虫の防除方法 |
| WO2011094581A1 (en) | 2010-01-29 | 2011-08-04 | North Carolina State University | Mosquito trap |
| WO2011094600A1 (en) * | 2010-01-29 | 2011-08-04 | North Carolina State University | Mosquito trap |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2607796A (en) * | 1951-08-03 | 1952-08-19 | Milton S Schechter | Crystalline isomer of allethrin |
| BE635902A (en, 2012) * | 1962-08-06 | |||
| US3402179A (en) * | 1965-01-25 | 1968-09-17 | Sumitomo Chemical Co | Phthalimidomethyl alkynyl ethers |
| DE1642339B1 (de) * | 1967-07-13 | 1972-01-13 | Sumitomo Chemical Co | Insektizide Mittel |
| JPS4817051B1 (en, 2012) * | 1969-11-19 | 1973-05-26 | ||
| ZA708448B (en) * | 1969-12-24 | 1971-09-29 | Sumitomo Chemical Co | Novel insecticidal compositions |
| BE786808A (fr) * | 1971-07-28 | 1973-01-29 | Johnson & Son Inc S C | Chrysanthemumates de benzyle |
| DE2326077C2 (de) * | 1972-05-25 | 1985-12-12 | National Research Development Corp., London | Ungesättigte Cyclopropancarbonsäuren und deren Derivate, deren Herstellung und diese enthaltende Insektizide |
| BR7303782D0 (pt) * | 1972-05-25 | 1973-12-20 | Nat Res Dev | Processo para a preparacao de um ester acido ciclo propano carboxilico composicao inseticida e processo para combater insetos |
-
1973
- 1973-10-18 JP JP11749773A patent/JPS5710842B2/ja not_active Expired
-
1974
- 1974-10-16 AU AU74379/74A patent/AU467738B2/en not_active Expired
- 1974-10-16 CS CS7400007095A patent/CS180027B2/cs unknown
- 1974-10-16 US US515332A patent/US3899586A/en not_active Expired - Lifetime
- 1974-10-16 CY CY1024A patent/CY1024A/xx unknown
- 1974-10-16 GB GB4482774A patent/GB1447193A/en not_active Expired
- 1974-10-17 NL NL7413648.A patent/NL161655C/xx not_active IP Right Cessation
- 1974-10-17 CH CH1393374A patent/CH604515A5/xx not_active IP Right Cessation
- 1974-10-17 DE DE2449546A patent/DE2449546C2/de not_active Expired
- 1974-10-17 DK DK544274AA patent/DK136343B/da not_active IP Right Cessation
- 1974-10-17 ES ES431108A patent/ES431108A1/es not_active Expired
- 1974-10-17 IT IT53611/74A patent/IT1050252B/it active
- 1974-10-17 CA CA211,615A patent/CA1031256A/en not_active Expired
- 1974-10-18 FR FR7435104A patent/FR2247974B1/fr not_active Expired
- 1974-10-18 AR AR256147A patent/AR224323A1/es active
- 1974-10-18 PL PL1974174918A patent/PL94420B1/pl unknown
- 1974-10-18 SU SU742073889A patent/SU631051A3/ru active
-
1978
- 1978-12-19 BE BE192402A patent/BE872872Q/xx not_active IP Right Cessation
-
1979
- 1979-01-02 DO DO1979002750A patent/DOP1979002750A/es unknown
- 1979-05-17 HK HK330/79A patent/HK33079A/xx unknown
- 1979-10-03 KE KE2995A patent/KE2995A/xx unknown
- 1979-12-30 MY MY176/79A patent/MY7900176A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| HK33079A (en) | 1979-05-25 |
| CH604515A5 (en, 2012) | 1978-09-15 |
| BE872872Q (fr) | 1979-04-17 |
| CS180027B2 (en) | 1977-12-30 |
| DK136343C (en, 2012) | 1978-02-27 |
| AU7437974A (en) | 1975-12-11 |
| FR2247974B1 (en, 2012) | 1976-10-22 |
| SU631051A3 (ru) | 1978-10-30 |
| US3899586A (en) | 1975-08-12 |
| FR2247974A1 (en, 2012) | 1975-05-16 |
| DK544274A (en, 2012) | 1975-06-16 |
| NL7413648A (nl) | 1975-04-22 |
| CY1024A (en) | 1980-08-01 |
| IT1050252B (it) | 1981-03-10 |
| AU467738B2 (en) | 1975-12-11 |
| DE2449546C2 (de) | 1982-02-11 |
| JPS5069231A (en, 2012) | 1975-06-10 |
| CA1031256A (en) | 1978-05-16 |
| NL161655B (nl) | 1979-10-15 |
| GB1447193A (en, 2012) | 1976-08-25 |
| JPS5710842B2 (en, 2012) | 1982-03-01 |
| DOP1979002750A (es) | 1990-06-27 |
| ES431108A1 (es) | 1976-11-01 |
| DE2449546A1 (de) | 1975-04-24 |
| KE2995A (en) | 1979-11-02 |
| NL161655C (nl) | 1980-03-17 |
| DK136343B (da) | 1977-10-03 |
| AR224323A1 (es) | 1981-11-30 |
| MY7900176A (en) | 1979-12-31 |
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