JPH09301810A - Insecticidal composition - Google Patents

Insecticidal composition

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Publication number
JPH09301810A
JPH09301810A JP12194396A JP12194396A JPH09301810A JP H09301810 A JPH09301810 A JP H09301810A JP 12194396 A JP12194396 A JP 12194396A JP 12194396 A JP12194396 A JP 12194396A JP H09301810 A JPH09301810 A JP H09301810A
Authority
JP
Japan
Prior art keywords
compound
methyl
formulation
parts
composition
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
Application number
JP12194396A
Other languages
Japanese (ja)
Inventor
Masaomi Ogawa
正臣 小川
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP12194396A priority Critical patent/JPH09301810A/en
Publication of JPH09301810A publication Critical patent/JPH09301810A/en
Pending legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To obtain an insecticidal composition exhibiting excellent effects against white flies resistant to various kinds of chemical agents by jointly using two kinds of known insecticides in a specific ratio. SOLUTION: This insecticidal composition contains 3-(4-ethoxyphenyl)-3- methyl-6-(4-fluoro-3-phenoxyphenyl)-1-hexyne and 0, 0-dimethyl-0-(3-methyl-4- nitrophenyl)phosphothioate in a weight ratio of 1:3 to 1:20. The composition is applied to insect pests or a place where the insect pests live. The two compounds as the active ingredients are mixed with various kinds of carriers, if necessary further with an additive and subsequently formed into a formulation such as powder, granules, emulsions, etc. The total amount of the active ingredients in the formulation is preferably approximately 0.1-95wt.%. The composition is especially effective for controlling white flies such as Bemisia tabaci and Trialeurodes vaporariorum.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は殺虫組成物に関す
る。
FIELD OF THE INVENTION The present invention relates to insecticidal compositions.

【従来の技術および発明が解決しようとする課題】従来
からコナジラミ類等の防除を目的とする殺虫剤の開発は
広く進められ、多種多様な薬剤が実用に供されている。
しかしながら、近年特にコナジラミ類は各種の薬剤に対
して抵抗性を迅速に発達させ、各種薬剤の効果を著しく
低下させており、特にコナジラミ類に優れた効果を示す
新しい殺虫剤が望まれている。
2. Description of the Related Art Conventionally, the development of insecticides for controlling whiteflies and the like has been extensively developed, and a wide variety of agents are put to practical use.
However, in recent years, whiteflies in particular have rapidly developed resistance to various drugs, and the effects of various drugs have been significantly reduced, and new insecticides showing excellent effects especially against whiteflies have been desired.

【0002】[0002]

【課題を解決するための手段】本発明者は、このような
状況に鑑み、優れた殺虫剤を開発すべく種々検討した結
果、(a) 3−(4−エトキシフェニル)−3−メチ
ル−6−(4−フルオロ−3−フェノキシフェニル)−
1−ヘキシンと(b) O,O−ジメチル−O−(3−
メチル−4−ニトロフェニル)ホスホロチオエートとを
重量比1:3〜1:20の割合で併用することにより、
特にコナジラミ類等に対し相乗的作用により優れた殺虫
効果を示すことを見い出し、本発明を完成させた。すな
わち、本発明は、(a) 3−(4−エトキシフェニ
ル)−3−メチル−6−(4−フルオロ−3−フェノキ
シフェニル)−1−ヘキシン(以下、化合物aと記
す。)と(b) O,O−ジメチル−O−(3−メチル
−4−ニトロフェニル)ホスホロチオエート(以下、化
合物bと記す。)とを有効成分として含有することを特
徴とする殺虫組成物(以下、本発明組成物と記す。)お
よび化合物aと化合物bとを重量比1:3〜1:20の
割合で害虫または害虫の生息場所に処理することを特徴
する殺虫方法を提供する。
In view of such circumstances, the present inventor has conducted various studies to develop an excellent insecticide, and as a result, (a) 3- (4-ethoxyphenyl) -3-methyl- 6- (4-fluoro-3-phenoxyphenyl)-
1-hexyne and (b) O, O-dimethyl-O- (3-
Methyl-4-nitrophenyl) phosphorothioate is used in combination at a weight ratio of 1: 3 to 1:20,
In particular, they have found that they have an excellent insecticidal effect by a synergistic action against whiteflies and the like, and completed the present invention. That is, the present invention provides (a) 3- (4-ethoxyphenyl) -3-methyl-6- (4-fluoro-3-phenoxyphenyl) -1-hexyne (hereinafter referred to as compound a) and (b). ) O, O-Dimethyl-O- (3-methyl-4-nitrophenyl) phosphorothioate (hereinafter, referred to as compound b) as an active ingredient, an insecticidal composition (hereinafter, the composition of the present invention). And a compound b at a weight ratio of 1: 3 to 1:20 are applied to pests or habitats of pests.

【0003】[0003]

【発明の実施の形態】化合物aは特開昭62−5928
号公報の第1表に記載された化合物(4)であり、該公
報に記載の方法等により製造することができる。化合物
aにはエチニル基が結合した不整炭素原子に基づく立体
(光学)異性体(R/S)が存在するが、本発明では殺
虫活性を有する立体異性体およびその混合物を使用する
ことができる。化合物bは例えばThe Pesticide Manual
(tenth edition;edited by Clive Tomlin;published b
y the British Crop Protection Council and the Roya
l Chemical Society,1994)435 頁に記載されている。
BEST MODE FOR CARRYING OUT THE INVENTION Compound a is disclosed in JP-A-62-5928.
It is the compound (4) described in Table 1 of the publication, and can be produced by the method described in the publication. Although compound a has a stereo (optical) isomer (R / S) based on an asymmetric carbon atom to which an ethynyl group is bonded, stereoisomers having insecticidal activity and mixtures thereof can be used in the present invention. Compound b can be prepared, for example, by The Pesticide Manual
(Tenth edition; edited by Clive Tomlin; published b
y the British Crop Protection Council and the Roya
l Chemical Society, 1994) p. 435.

【0004】本発明組成物はタバココナジラミ(Bemisia
tabaci) 、オンシツコナジラミ(Trialeurodes vapora
riorum) 等のコナジラミ類の防除に特に有効であるが、
その他の害虫、例えば、シラホシカメムシ(Eysarcoris
ventralis)、トゲシラホシカメムシ(Eysarcoris parvu
s) 、オオトゲシラホシカメムシ (Eysarcoris lewis
i)、アオクサカメムシ(Nezara antennata)、ミナミアオ
カメムシ(Nezara viridula) 、ホソヘリカメムシ(Ripto
rtus clavatus)、ホソハリカメムシ(Cletus punctige
r)、クモヘリカメムシ(Leptocorisa chinensis) 等のカ
メムシ類、ツマグロヨコバイ(Nephotettix cincticep
s)、トビイロウンカ(Nilaparvata lugens)、ヒメトビウ
ンカ(Laodelphax striatellus)、セジロウンカ(Sogatel
la furcifera) 等の半翅目害虫;コブノメイガ(Cnaphal
ocrocis medinalis)、ニカメイチュウ(Chilo suppressa
lis)、イネツトムシ(Parnara guttata) 等の鱗翅目害
虫;イネミズゾウムシ(Lissorhoptrus oryzophilus) 、
イネゾウムシ(Echinocnemus squameus) 、イネドロオイ
ムシ(Oulema oryzae) 等の甲虫目害虫;コバネイナゴ(O
xya yezoensis)等の直翅目害虫等の防除にも有効であ
る。
The composition of the present invention is a whitefly for Bemisia tabaci (Bemisia).
tabaci), Whitefly (Trialeurodes vapora)
riorum) is especially effective in controlling whiteflies such as
Other pests, such as the beetle stink bug (Eysarcoris)
ventralis), Prickly stink bug (Eysarcoris parvu)
s), Stinkbill, Eysarcoris lewis
i), Green stink bug (Nezara antennata), Southern green stink bug (Nezara viridula), Rapto helicopter bug (Ripto)
rtus clavatus), the stink bug, Cletus punctige
r), stink bugs such as Leptocorisa chinensis, and leafhoppers (Nephotettix cincticep)
s), the brown planthopper (Nilaparvata lugens), the brown planthopper (Laodelphax striatellus), and the white-bellied planthopper (Sogatel)
Hemiptera pests such as la furcifera; Cnaphal
ocrocis medinalis), Nikameichu (Chilo suppressa
lis), lepidopteran pests such as beetles (Parnara guttata); rice weevil (Lissorhoptrus oryzophilus),
Coleoptera insect pests such as rice weevil (Echinocnemus squameus) and rice duck beetle (Oulema oryzae);
It is also effective for the control of orthoptera pests such as xya yezoensis).

【0005】本発明において、有効成分として用いられ
る化合物aおよび化合物bは、他の何らの成分も加え
ず、そのまま使用してもよいが、通常は、両有効成分を
固体担体、液体担体、ガス状担体等の各種担体と混合
し、必要あれば添加剤として界面活性剤、分散剤、固着
剤、安定化剤、噴射剤、その他の製剤用補助剤を加え
て、粉剤、粒剤、乳剤、油剤、水和剤、顆粒水和剤、水
溶性フィルム包装製剤、ゾル剤、フロアブル剤、エアゾ
ール剤、塗布剤、燻煙剤、燻蒸剤、ULV剤等の製剤形
態に製剤し必要に応じさらに水で希釈して使用するか、
あるいは、各々の有効成分をあらかじめ上記のような各
種製剤形態に製剤した後混合しまたは混合せずに同時に
使用すること、あるいは各々の有効成分をあらかじめ上
記のような各種製剤形態に製剤しさらに水で希釈して各
々の薬液に調製した後に混合しまたは混合せずに同時に
使用することもできる。これらの製剤中の全有効成分量
は重量比で通常0.1〜95%である。製剤の際に用いら
れる固体担体としては、たとえば粘土類(カオリンクレ
ー、珪藻土、合成含水酸化珪素、ベントナイト、フバサ
ミクレー、酸性白土等)、タルク類、セラミック、その
他の無機鉱物(セリサイト、石英、硫黄、活性炭、炭酸
カルシウム、水和シリカ等)、化学肥料(硫安、燐安、
硝安、尿素、塩安等)等の微粉末あるいは粒状物等があ
げられ、液体担体としては、たとえば水、アルコール類
(メタノール、エタノール等)、ケトン類(アセトン、
メチルエチルケトン等)、芳香族炭化水素類(ベンゼ
ン、トルエン、キシレン、エチルベンゼン、メチルナフ
タレン等)、脂肪族炭化水素類(ヘキサン、シクロヘキ
サン、灯油、軽油等)、エステル類(酢酸エチル、酢酸
ブチル等)、ニトリル類(アセトニトリル、イソブチロ
ニトリル等)、エーテル類(ジイソプロピルエーテル、
ジオキサン等)、酸アミド類(N,N−ジメチルホルム
アミド、N,N−ジメチルアセトアミド等)、ハロゲン
化炭化水素類(ジクロロメタン、トリクロロエタン、四
塩化炭素等)、ジメチルスルホキシド、大豆油、綿実油
等の植物油等があげられ、ガス状担体、すなわち噴霧剤
としては、たとえばフロンガス、ブタンガス、LPG
(液化石油ガス)、ジメチルエーテル、炭酸ガス等があ
げられる。界面活性剤としては、たとえばアルキル硫酸
エステル塩、アルキルスルホン酸塩、アルキルアリール
スルホン酸塩、アルキルアリールエーテル類およびその
ポリオキシエチレン化物、ポリエチレングリコールエー
テル類、多価アルコールエステル類、糖アルコール誘導
体等があげられる。固着剤や分散剤等の製剤用補助剤と
しては、たとえばカゼイン、ゼラチン、多糖類(でんぷ
ん粉、アラビアガム、セルロース誘導体、アルギン酸
等)、リグニン誘導体、ベントナイト、糖類、合成水溶
性高分子(ポリビニルアルコール、ポリビニルピロリド
ン、ポリアクリル酸類等)等があげられ、安定剤として
は、たとえばPAP(酸性リン酸イソプロピル)、BH
T(2,6−ジ−tert−ブチル−4−メチルフェノー
ル)、BHA(2−tert−ブチル−4−メトキシフェノ
ールと3−tert−ブチル−4−メトキシフェノールとの
混合物)、植物油、鉱物油、界面活性剤、脂肪酸または
そのエステル等があげられる。
In the present invention, the compound a and the compound b used as the active ingredients may be used as they are without adding any other ingredients, but usually, both active ingredients are solid carrier, liquid carrier, gas. Powders, granules, emulsions, by mixing with various carriers such as a granular carrier, and if necessary, adding a surfactant, a dispersant, a sticking agent, a stabilizer, a propellant, and other formulation auxiliary agents as additives. Formulations such as oils, wettable powders, wettable granules, water-soluble film packaging preparations, sols, flowable agents, aerosols, coating agents, fumigants, fumigants, ULV agents, etc. Or dilute with
Alternatively, each active ingredient is formulated in advance in various formulation forms as described above and then mixed or used simultaneously without mixing, or each active ingredient is formulated in advance in various formulation forms as described above and further mixed with water. It is also possible to dilute with and prepare each drug solution, and then mix or mix and use them simultaneously. The total amount of active ingredients in these preparations is usually 0.1 to 95% by weight. Examples of solid carriers used in the preparation include clays (kaolin clay, diatomaceous earth, synthetic hydrous silicon oxide, bentonite, fubasami clay, acid clay, etc.), talc, ceramics, and other inorganic minerals (sericite, quartz, sulfur). , Activated carbon, calcium carbonate, hydrated silica, etc., chemical fertilizers (ammonium sulfate, phosphorus ammonium,
Examples of the liquid carrier include water, alcohols (methanol, ethanol, etc.), ketones (acetone, acetone, etc.).
Methyl ethyl ketone, etc.), aromatic hydrocarbons (benzene, toluene, xylene, ethylbenzene, methylnaphthalene, etc.), aliphatic hydrocarbons (hexane, cyclohexane, kerosene, light oil, etc.), esters (ethyl acetate, butyl acetate, etc.), Nitriles (acetonitrile, isobutyronitrile, etc.), ethers (diisopropyl ether,
Dioxane), acid amides (N, N-dimethylformamide, N, N-dimethylacetamide, etc.), halogenated hydrocarbons (dichloromethane, trichloroethane, carbon tetrachloride, etc.), dimethyl sulfoxide, soybean oil, vegetable oil such as cottonseed oil Examples of the gaseous carrier, that is, the propellant include CFC gas, butane gas, and LPG.
(Liquefied petroleum gas), dimethyl ether, carbon dioxide gas and the like. Examples of the surfactant include alkyl sulfates, alkyl sulfonates, alkyl aryl sulfonates, alkyl aryl ethers and polyoxyethylenates thereof, polyethylene glycol ethers, polyhydric alcohol esters, sugar alcohol derivatives and the like. can give. Examples of pharmaceutical auxiliaries such as fixatives and dispersants include casein, gelatin, polysaccharides (starch, gum arabic, cellulose derivatives, alginic acid, etc.), lignin derivatives, bentonite, sugars, synthetic water-soluble polymers (polyvinyl alcohol). , Polyvinyl pyrrolidone, polyacrylic acids, etc.), and examples of the stabilizer include PAP (acidic isopropyl phosphate), BH
T (2,6-di-tert-butyl-4-methylphenol), BHA (mixture of 2-tert-butyl-4-methoxyphenol and 3-tert-butyl-4-methoxyphenol), vegetable oil, mineral oil , A surfactant, a fatty acid or an ester thereof, and the like.

【0006】このようにして得られる製剤は、そのまま
であるいは水等で希釈して用いる。また、他の殺虫剤、
殺線虫剤、殺ダニ剤、殺菌剤、除草剤、植物生長調節
剤、共力剤、肥料、土壌改良剤、動物用飼料等と混合し
て、または混合せずに同時に用いることもできる。本発
明組成物は、通常害虫あるいは果樹、蔬菜、棉、花き等
の農園芸作物や樹木等の害虫が生息する場所に、直接、
または機具を用いて、散布、噴霧、燻蒸等の方法により
施用することができる。本発明において、有効成分の施
用量は、10アールあたりの全有効成分量で、通常約
0.1g〜約1000gであり、好ましくは約1g〜約
500gである。乳剤、水和剤、フロアブル剤等を水で
希釈して用いる場合は、その施用濃度は通常、約3ppm
〜約3,000ppmであり、粉剤、エアゾール剤、ULV剤等
は、通常何ら希釈することなく製剤のままで施用する。
これらの施用量、施用濃度は、いずれも、製剤の形態、
施用時期、施用場所、施用方法、対象害虫の種類、被害
程度等の状況によって異なり、上記の範囲にかかわるこ
となく増加させたり、減少させたりすることができる。
The thus obtained preparation is used as it is or after diluted with water or the like. Also other pesticides,
They can be used together with or without mixing with nematicides, acaricides, fungicides, herbicides, plant growth regulators, synergists, fertilizers, soil conditioners, animal feeds and the like. The composition of the present invention is usually a pest or a fruit tree, a vegetable, a cotton, a plant, a place where a pest such as an agricultural and horticultural crop such as a tree or a tree inhabits, directly,
Alternatively, it can be applied by a method such as spraying, spraying, fumigation using a device. In the present invention, the amount of the active ingredient applied is, in terms of the total amount of the active ingredient per 10 ares, usually about 0.1 g to about 1000 g, preferably about 1 g to about 500 g. When emulsions, wettable powders, flowable agents, etc. are diluted with water, the application concentration is usually about 3 ppm.
It is about 3,000 ppm, and powders, aerosols, ULVs, etc. are usually applied as they are without any dilution.
These application rates and application concentrations are all in the form of formulation,
It can be increased or decreased without depending on the above range, depending on the conditions such as application time, application place, application method, type of target pest, and degree of damage.

【0007】[0007]

【実施例】以下、本発明を製剤例および試験例によりさ
らに詳しく説明するが、本発明はこれらの例に限定され
るものではない。なお、化合物aはすべてラセミ体(R
S体)を用い、製剤例において部とあるのはすべて重量
部を表わす。 製剤例1 粉剤 化合物a 0.2部、化合物b 2部、合成含水酸化珪
素2部、タルク45.8部およびクレー50部を均一に
混合して粉剤を得る。 製剤例2 乳剤 化合物a 10部、化合物b 50部、ポリオキシエチ
レンアルキルアリールエーテル9部、アルキルアリール
スルホン酸カルシウム1部およびキシレン30部を均一
に撹拌混合して乳剤を得る。 製剤例3 水和剤 化合物a 10部、化合物b 40部、合成含水酸化珪
素35部、アルキルベンゼンスルホン酸ナトリウム3
部、リグニンスルホン酸ナトリウム2部および珪藻土1
0部をジュースミキサーで均一に混合した後、エアーミ
ルで粉砕して、水和剤を得る。 製剤例4 フロアブル剤 ポリビニルアルコール4部を水41部中に加えて均一に
溶解し、これに化合物a 5部と化合物b 20部を加
えてホモジナイザーでよく攪拌した後、これにザンサン
ガム0.2部とスメクタイト系鉱物質0.4部を水2
9.4部に均一に溶解、分散した液を加えてフロアブル
剤を得る。
EXAMPLES The present invention will be described in more detail below with reference to formulation examples and test examples, but the present invention is not limited to these examples. All the compounds a are racemic (R
(S-form), all parts in formulation examples are parts by weight. Formulation Example 1 Dust: 0.2 part of compound a, 2 parts of compound b, 2 parts of synthetic hydrous silicon oxide, 45.8 parts of talc and 50 parts of clay are uniformly mixed to obtain a powder. Formulation Example 2 Emulsion 10 parts of compound a, 50 parts of compound b, 9 parts of polyoxyethylene alkylaryl ether, 1 part of alkylaryl sulfonate and 1 part of xylene are uniformly stirred and mixed to obtain an emulsion. Formulation Example 3 Wettable powder 10 parts of compound a, 40 parts of compound b, 35 parts of synthetic hydrous silicon oxide, sodium alkylbenzenesulfonate 3
Parts, 2 parts sodium lignin sulfonate and 1 diatomaceous earth
After uniformly mixing 0 parts with a juice mixer, it is pulverized with an air mill to obtain a wettable powder. Formulation Example 4 Flowable agent Polyvinyl alcohol (4 parts) was added to water (41 parts) to uniformly dissolve it, and compound (5 parts) and compound (b) (20 parts) were added thereto, and the mixture was thoroughly stirred with a homogenizer, and then 0.2 part of zansan gum was added. And 0.4 parts of smectite minerals in water 2
A uniformly dissolved and dispersed liquid is added to 9.4 parts to obtain a flowable agent.

【0008】次に、本発明により、化合物aや化合物b
を各々単独で用いたときと比較して、相乗作用により優
れた殺虫効果が得られることを試験例により示す。
Next, according to the present invention, compound a and compound b
It is shown by a test example that an excellent insecticidal effect can be obtained by a synergistic effect, as compared with the case where each of these is used alone.

【0009】試験例1 製剤例2に準じて乳剤として製剤された化合物a(有効
成分量10%)および乳剤として製剤された化合物b
(住友化学工業株式会社製スミチオン50%乳剤)の各
々を水で希釈し、該希釈液を所定の有効成分濃度になる
ように混合して、供試薬剤を得た。尚、上記の乳剤とし
て製剤された化合物aおよび乳剤として製剤された化合
物bの各々を比較対照薬剤として供試した。ポリエチレ
ンカップ植えのキャベツ(3葉期)に、上記の供試薬剤
を1カップあたり30ml散布した。風乾後、葉を切り取
り、プラスチックシャーレ (直径9cm、深さ2cm) に1
枚ずつ入れ、その後タバココナジラミ成虫を1シャーレ
あたり約50頭放虫した(1区3反復)。シャーレを2
5℃の実験室内に保持し、2日後に生死を調査し、殺虫
率を算出した。その結果を表1に示す。
Test Example 1 Compound a (10% active ingredient amount) formulated as an emulsion and compound b formulated as an emulsion according to Formulation Example 2
Each of (Sumition Chemical Co., Ltd., Sumithion 50% emulsion) was diluted with water, and the diluted solution was mixed so as to have a predetermined active ingredient concentration to obtain a reagent. Each of the compound a prepared as an emulsion and the compound b prepared as an emulsion was used as a comparative control drug. To the cabbage (three leaves stage) planted in a polyethylene cup, 30 ml per cup of the above reagent was sprayed. After air-drying, cut the leaves and put 1 on a plastic petri dish (9 cm in diameter, 2 cm in depth).
About 50 head whitefly adults were released per petri dish (1 group, 3 repetitions). 2 petri dishes
It was kept in a laboratory at 5 ° C., and after 2 days, life and death was examined and the insecticidal rate was calculated. Table 1 shows the results.

【表1】 [Table 1]

【0010】試験例2 製剤例1により得られた粉剤を供試薬剤として用いた。
尚、製剤例1に準じて粉剤として製剤された化合物a
(有効成分量0.2%)および粉剤として製剤された化
合物b(北興化学工業株式会社製スミチオン粉剤20:
有効成分量2%)の各々を比較対照薬剤として供試し
た。逃亡防止のためナイロンゴースで周囲を覆った1/
10000アールのワグネルポット植えのイネに1ポッ
トあたりトビイロウンカ成虫10頭(雄雌各5頭)を放
飼し、3日間産卵させた。その後、成虫を除去し、ベル
ジャーダスター(散粉機)用いて供試薬剤を3kg粉剤
/10アール相当量散布した(1区3反復)。処理3週
間後に次世代の生存幼虫数を調査し、その抑制率を算出
した。その結果を表2に示す。
Test Example 2 The powder obtained in Formulation Example 1 was used as a reagent.
Compound a prepared as a powder according to Formulation Example 1
(Active ingredient amount 0.2%) and compound b formulated as a powder (Hokuko Kagaku Kogyo Co., Ltd. Sumithion powder 20:
Each of the active ingredients (2%) was used as a comparative control drug. Covered with nylon ghost to prevent escape 1 /
Ten rice planthoppers (5 males and 5 females) were released per pot in rice planted with a Wagner pot of 10,000 are and laid for 3 days. After that, the adults were removed, and the reagent mixture was sprayed using a bell jar duster (dusting machine) in an amount corresponding to 3 kg of dust / 10 ares (1 group, 3 repetitions). Three weeks after the treatment, the number of surviving larvae of the next generation was investigated and the suppression rate was calculated. The results are shown in Table 2.

【表2】 [Table 2]

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】(a) 3−(4−エトキシフェニル)−
3−メチル−6−(4−フルオロ−3−フェノキシフェ
ニル)−1−ヘキシンと(b) O,O−ジメチル−O
−(3−メチル−4−ニトロフェニル)ホスホロチオエ
ートとを重量比1:3〜1:20の割合で有効成分とし
て含有することを特徴する殺虫組成物。
1. (a) 3- (4-ethoxyphenyl)-
3-Methyl-6- (4-fluoro-3-phenoxyphenyl) -1-hexyne and (b) O, O-dimethyl-O
An insecticidal composition comprising-(3-methyl-4-nitrophenyl) phosphorothioate as an active ingredient in a weight ratio of 1: 3 to 1:20.
【請求項2】(a) 3−(4−エトキシフェニル)−
3−メチル−6−(4−フルオロ−3−フェノキシフェ
ニル)−1−ヘキシンと(b) O,O−ジメチル−O
−(3−メチル−4−ニトロフェニル)ホスホロチオエ
ートとを重量比1:3〜1:20の割合で害虫または害
虫の生息場所に処理することを特徴する殺虫方法。
2. (a) 3- (4-ethoxyphenyl)-
3-Methyl-6- (4-fluoro-3-phenoxyphenyl) -1-hexyne and (b) O, O-dimethyl-O
An insecticidal method, which comprises treating pests or habitats of pests with-(3-methyl-4-nitrophenyl) phosphorothioate at a weight ratio of 1: 3 to 1:20.
JP12194396A 1996-05-16 1996-05-16 Insecticidal composition Pending JPH09301810A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12194396A JPH09301810A (en) 1996-05-16 1996-05-16 Insecticidal composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12194396A JPH09301810A (en) 1996-05-16 1996-05-16 Insecticidal composition

Publications (1)

Publication Number Publication Date
JPH09301810A true JPH09301810A (en) 1997-11-25

Family

ID=14823773

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12194396A Pending JPH09301810A (en) 1996-05-16 1996-05-16 Insecticidal composition

Country Status (1)

Country Link
JP (1) JPH09301810A (en)

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