AU564889B2 - Method for control of soil-borne insects - Google Patents
Method for control of soil-borne insectsInfo
- Publication number
- AU564889B2 AU564889B2 AU49525/85A AU4952585A AU564889B2 AU 564889 B2 AU564889 B2 AU 564889B2 AU 49525/85 A AU49525/85 A AU 49525/85A AU 4952585 A AU4952585 A AU 4952585A AU 564889 B2 AU564889 B2 AU 564889B2
- Authority
- AU
- Australia
- Prior art keywords
- soil
- cis
- compound
- chloro
- compounds
- 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.)
- Ceased
Links
- 241000238631 Hexapoda Species 0.000 title claims description 16
- 238000000034 method Methods 0.000 title claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 39
- 239000002689 soil Substances 0.000 claims description 28
- 239000000203 mixture Substances 0.000 claims description 16
- 239000004480 active ingredient Substances 0.000 claims description 12
- -1 difluorophenylmethyl Chemical group 0.000 claims description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- MEFBHJDTCCDZGW-UHFFFAOYSA-N (2-fluorophenyl)methyl 3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(Cl)C(F)(F)F)C1C(=O)OCC1=CC=CC=C1F MEFBHJDTCCDZGW-UHFFFAOYSA-N 0.000 claims 1
- 150000007942 carboxylates Chemical class 0.000 claims 1
- YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical compound OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 238000012360 testing method Methods 0.000 description 20
- 241000489976 Diabrotica undecimpunctata howardi Species 0.000 description 11
- 238000009472 formulation Methods 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 230000036515 potency Effects 0.000 description 6
- 229920003023 plastic Polymers 0.000 description 5
- 239000004033 plastic Substances 0.000 description 5
- 238000010348 incorporation Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 241001136249 Agriotes lineatus Species 0.000 description 3
- 241001529600 Diabrotica balteata Species 0.000 description 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 3
- 230000000749 insecticidal effect Effects 0.000 description 3
- 230000001418 larval effect Effects 0.000 description 3
- 239000011550 stock solution Substances 0.000 description 3
- 241000566547 Agrotis ipsilon Species 0.000 description 2
- 241000683561 Conoderus Species 0.000 description 2
- 241000732728 Ctenicera aeripennis Species 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 206010061217 Infestation Diseases 0.000 description 2
- 241001394950 Melanotus communis (Gyllenhal, 1817) Species 0.000 description 2
- 241000254101 Popillia japonica Species 0.000 description 2
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- YMGUBTXCNDTFJI-UHFFFAOYSA-M cyclopropanecarboxylate Chemical compound [O-]C(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-M 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000012085 test solution Substances 0.000 description 2
- HQPKNQLXQWODSE-UHFFFAOYSA-N (2,4,6-trifluorophenyl)methyl 3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(Cl)C(F)(F)F)C1C(=O)OCC1=C(F)C=C(F)C=C1F HQPKNQLXQWODSE-UHFFFAOYSA-N 0.000 description 1
- LVICICZQETYOGS-UHFFFAOYSA-N (2,6-difluorophenyl)methanol Chemical group OCC1=C(F)C=CC=C1F LVICICZQETYOGS-UHFFFAOYSA-N 0.000 description 1
- DYLIWHYUXAJDOJ-OWOJBTEDSA-N (e)-4-(6-aminopurin-9-yl)but-2-en-1-ol Chemical compound NC1=NC=NC2=C1N=CN2C\C=C\CO DYLIWHYUXAJDOJ-OWOJBTEDSA-N 0.000 description 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- 125000004847 2-fluorobenzyl group Chemical group [H]C1=C([H])C(F)=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 description 1
- 241000489973 Diabrotica undecimpunctata Species 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 241000258937 Hemiptera Species 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- 241000255777 Lepidoptera Species 0.000 description 1
- 241001062280 Melanotus <basidiomycete fungus> Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 101150054830 S100A6 gene Proteins 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 239000004148 curcumin Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000002316 fumigant Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000013207 serial dilution Methods 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US65938484A | 1984-10-10 | 1984-10-10 | |
US659384 | 1984-10-10 |
Publications (2)
Publication Number | Publication Date |
---|---|
AU4952585A AU4952585A (en) | 1986-05-02 |
AU564889B2 true AU564889B2 (en) | 1987-08-27 |
Family
ID=24645184
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU49525/85A Ceased AU564889B2 (en) | 1984-10-10 | 1985-10-01 | Method for control of soil-borne insects |
Country Status (13)
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2831193A1 (de) * | 1978-07-15 | 1980-01-24 | Bayer Ag | Fluoralkenylsubstituierte cyclopropancarbonsaeureester und ihre verwendung als insektizide |
DE2965291D1 (en) * | 1978-10-27 | 1983-06-01 | Ici Plc | Halogenated esters of cyclopropane acids, their preparation, compositions and use as pesticides |
ZA795532B (en) * | 1978-10-27 | 1980-09-24 | Ici Ltd | Halogenated esters of cyclopropane acids,their preparation compositions and use as pesticides |
US4332815A (en) * | 1979-06-25 | 1982-06-01 | Fmc Corporation | Insecticidal perhaloalkylvinylcyclopropanecarboxylates |
EP0031199B1 (en) * | 1979-12-21 | 1983-12-14 | Imperial Chemical Industries Plc | Substituted benzyl esters of cyclopropane carboxylic acids and their preparation, compositions containing them and methods of combating insect pests therewith, and substituted benzyl alcohols |
-
1985
- 1985-10-01 AU AU49525/85A patent/AU564889B2/en not_active Ceased
- 1985-10-01 BR BR8506967A patent/BR8506967A/pt unknown
- 1985-10-01 HU HU855033A patent/HUT41236A/hu unknown
- 1985-10-01 WO PCT/US1985/001898 patent/WO1986002238A1/en not_active Application Discontinuation
- 1985-10-01 JP JP60504542A patent/JPS61501709A/ja active Pending
- 1985-10-01 EP EP19850905156 patent/EP0197115A4/en not_active Withdrawn
- 1985-10-06 IL IL76595A patent/IL76595A/xx unknown
- 1985-10-08 AR AR85301877A patent/AR247656A1/es active
- 1985-10-08 GR GR852434A patent/GR852434B/el unknown
- 1985-10-08 CN CN85107462A patent/CN1009417B/zh not_active Expired
-
1986
- 1986-06-09 BG BG075271A patent/BG51231A3/bg unknown
- 1986-06-09 DK DK269286A patent/DK269286D0/da not_active Application Discontinuation
- 1986-06-10 KR KR1019860700343A patent/KR870700285A/ko not_active Ceased
Also Published As
Publication number | Publication date |
---|---|
KR870700285A (ko) | 1987-12-28 |
BR8506967A (pt) | 1986-12-23 |
HUT41236A (en) | 1987-04-28 |
BG51231A3 (bg) | 1993-03-30 |
EP0197115A4 (en) | 1989-08-29 |
DK269286A (da) | 1986-06-09 |
CN85107462A (zh) | 1986-06-10 |
JPS61501709A (ja) | 1986-08-14 |
DK269286D0 (da) | 1986-06-09 |
GR852434B (enrdf_load_stackoverflow) | 1986-02-10 |
AR247656A1 (es) | 1995-03-31 |
EP0197115A1 (en) | 1986-10-15 |
IL76595A (en) | 1988-11-30 |
AU4952585A (en) | 1986-05-02 |
WO1986002238A1 (en) | 1986-04-24 |
CN1009417B (zh) | 1990-09-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4889872A (en) | 2,3,5,6-Tetrafluorobenzyl (+) 1r-trans-2,2-dimethyl-3-(2,2-dichlorovinyl)-cyclopropanecarboxylate | |
US4263319A (en) | 4-Substituted-2-indanol insecticidal ester derivatives | |
US4503071A (en) | Insecticidal composition containing optically active α-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)isovalerate | |
AU2006330918B2 (en) | Insecticidal and miticidal mixtures of bifenthrin and cyano-pyrethroids | |
NZ199084A (en) | Fluoro-benzyl esters of cyclopropane carboxylic acids and insecticidal compositions | |
JPH04154740A (ja) | ハロゲン化オレフィン、これを含有する殺虫剤および殺ダニ剤ならびに虫およびダニを駆除する方法 | |
US4376785A (en) | Cyclopropanecarboxylates and a low fish toxic insecticide and/or acaricide containing them | |
CA1125653A (en) | Low mammalian toxic and/or low fish toxic insecticidal and/or acaricidal composition | |
JPH05112519A (ja) | 3−[2−シアノ−2−ハロゲノエテニル−2,2−ジメチルシクロプロパンカルボン酸の新エステル誘導体、それらの製造法及び殺生物としての使用 | |
DE69026906T2 (de) | Arylpyrrol enthaltende insekticidale, acaricidale und nematicidale Mittel sowie Verfahren zu ihrer Herstellung | |
AU564889B2 (en) | Method for control of soil-borne insects | |
US4709068A (en) | Substituted phenyltrialkylsilane insecticides | |
KR930007305B1 (ko) | 카복실산 에스테르의 제조방법 | |
DE69916752T2 (de) | 2-Aryl-Delta 2-1,3,4-(oxa oder thia)Diazoline enthaltende Insektizide und akarizide Mittel | |
CA1125303A (en) | Insecticidal alpha-trifluoromethyl-3-phenoxybenzyl carboxylates | |
JPS60142906A (ja) | 屋内ダニ防除用液剤ならびにエアゾール剤 | |
US4758590A (en) | Method for control of soil-borne insects | |
US4335252A (en) | Insecticidal pyrethroid enantiomer pair | |
JP3320453B2 (ja) | 4−アミノ−2,3,5,6−テトラフルオルフェニルメチルアルコールの新規なピレスリノイドエステル、それらの製造法及びそれらのペスチサイドとしての用途 | |
US4997855A (en) | Vinyl fluorides and pesticidal uses | |
US4162366A (en) | α-TRIFLUOROMETHYL-3-PHENOXYBENZYL ALCOHOL | |
GB2037282A (en) | Low mammalian toxic and/or low fish toxic insecticides and/or acaricides | |
EP0061713B1 (en) | Cyclopropanecarboxylic acid esters, their production and insecticidal and acaricidal compositions containing them | |
CH647224A5 (de) | Substituierter benzylester einer 2,2-dimethyl-3-(2,2-dihalogenvinyl)cyclopropancarbonsaeure. | |
JP3233696B2 (ja) | 新規カルボン酸エステル誘導体、及びこれを含有する殺虫、殺ダニ剤 |