JPS6226208A - Attractant and insecticidal composition for fly - Google Patents

Attractant and insecticidal composition for fly

Info

Publication number
JPS6226208A
JPS6226208A JP60166359A JP16635985A JPS6226208A JP S6226208 A JPS6226208 A JP S6226208A JP 60166359 A JP60166359 A JP 60166359A JP 16635985 A JP16635985 A JP 16635985A JP S6226208 A JPS6226208 A JP S6226208A
Authority
JP
Japan
Prior art keywords
cis
flies
tricosene
parts
trans
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.)
Granted
Application number
JP60166359A
Other languages
Japanese (ja)
Other versions
JPH0560441B2 (en
Inventor
Tsutomu Negishi
務 根岸
Masaharu Kamei
正治 亀井
Masaru Nishikawa
勝 西川
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.)
Earth Corp
Original Assignee
Earth 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 Earth Chemical Co Ltd filed Critical Earth Chemical Co Ltd
Priority to JP60166359A priority Critical patent/JPS6226208A/en
Priority to BR8606797A priority patent/BR8606797A/en
Priority to EP86904389A priority patent/EP0229191B1/en
Priority to PCT/JP1986/000373 priority patent/WO1987000401A1/en
Priority to KR1019870700238A priority patent/KR940000802B1/en
Priority to DE86904389T priority patent/DE3688525T2/en
Priority to AU61368/86A priority patent/AU591161B2/en
Priority to US07/031,068 priority patent/US4855133A/en
Publication of JPS6226208A publication Critical patent/JPS6226208A/en
Publication of JPH0560441B2 publication Critical patent/JPH0560441B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:The titled composition containing (5-benzyl-3-furyl)methyl d-cis/trans- chrysanthemate, etc., and a sexual attractant substance, e.g. 9-tricosene, etc., in combination and capable of attracting flies for a time sufficient to produce insecticidal efficacy. CONSTITUTION:An attractant and insecticidal composition for flies containing particularly at least one of (5-benzyl-3-furyl)methyl d-cis/trans-chrysanthemate, 3-phenoxybenzyl d-cis/trans-chrysanthemate or 3-phenoxybenzyl dl-cis/trans-3-(2,2- dichlorovinyl)-2,2-dimethyl-1-cyclopro-panecarboxylate in pyrethroid based compounds and one selected from 9-tricosene, cis-9-tricosene, 10-methyl-9- tricosene, etc., as active constituents. EFFECT:Effective even for flies having resistance.

Description

【発明の詳細な説明】 髪末上辺fig匁1 本発明は、ハエ用誘引殺虫剤組成物に関する。[Detailed description of the invention] Upper end of hair fig momme 1 The present invention relates to a fly attractant and insecticide composition.

従来の技術及びその問題点 ハエ成虫の駆除剤としては、従来より例えば乳剤、油剤
、エアゾール剤、食毒剤等が知られており、之等のうち
乳剤、油剤及びエアゾール剤については、近年殺虫活性
に優れ且つ人畜に対する安全性の高い殺虫剤が開発され
、これが上記各秤の剤型に応用され実用されるに至って
いる。しかし食毒剤については、フライマット他2〜3
の商品が存在するが、実用上満足できる製品は開発され
るに至っていない。
Conventional technology and its problems As insecticidal agents for adult flies, for example, emulsions, oils, aerosols, food poisons, etc. have been known for a long time. Insecticides with excellent activity and high safety for humans and livestock have been developed, and these have been applied to the dosage forms of the above-mentioned scales and put into practical use. However, regarding food poisons, Frymat et al.
There are several products available, but no product that is practically satisfactory has yet been developed.

該食毒剤(毒餌剤)とは、ハエの餌となるものに殺虫剤
を含浸乃至含有させたものであるが、その処方の選択、
毒餌剤の調製等に当っては、実用性を考慮すると、以下
の如き非常に高度の技術が要求される。即ち、まず第1
に選択される殺虫剤成分がハエに対してできるだけ忌避
性を持たないこと、第2にその毒餌にハエを誘引するた
めの物理的及び(又は)化学的な手段を必要とすること
、第3に毒餌に飛来したハエが摂食行動を開始するよう
にハエにとって充分な味覚的誘惑性があること、第4に
毒餌を摂食し始めてから何らかの嫌気性や中毒症状が発
現するまでに、ハエに充分な致死量を取込ませ得ること
、等で必る。勿論上記各要件は、個々に別個のものでは
なく、相互に密接に関連している。2等要件のいずれか
一つでも欠けると、得られる毒餌剤の有効性は極端に劣
悪となり、満足な結果は得られない。
The food poison (poison bait) is a food for flies that is impregnated with or contains an insecticide, and the selection of its formulation,
When preparing poisonous baits, etc., considering practicality, the following extremely sophisticated techniques are required. That is, first
secondly, the insecticide component selected must have as little repellency as possible to flies; secondly, it requires physical and/or chemical means to attract flies to the poisonous bait; and thirdly Fourthly, there must be enough gustatory attraction for the flies to start feeding when they land on the poisoned bait.Fourthly, the flies must have sufficient gustatory attraction to the poisoned bait before any anaerobic or intoxication symptoms develop. It is necessary to be able to introduce a sufficient lethal dose. Of course, each of the above requirements is not individual and is closely related to each other. If any one of the second-class requirements is missing, the effectiveness of the resulting poison bait will be extremely poor, and no satisfactory results will be obtained.

また、現在知られている毒餌剤の殺虫成分としては、有
機燐系又はカーバメート系殺虫剤のある種のものが利用
されているのみであり、ピレスロイド系殺虫剤は一般に
利用されていない。即ち、ピレスロイド系殺虫剤は慨し
て、ハエ成虫(以下単にハエという)に対して速効的に
作用し、優れたノックダウン効力を有することが知られ
ているが、これはハエの皮膚ヤ気門から体内に入って神
経系に極めて速やかに作用する特性を持っており、従っ
てその応用は気門呼吸経路及び皮膚接触経路に限られて
いる。ハエに限らず蚊やゴキブリ等に対しても、ピレス
ロイド系殺虫剤は、上記特性より例えば蚊取線香(空気
同経路)、電気蚊取マット(同上)、エアゾール(空気
門経路及び接触経路)、燻煙・蒸散剤(同上)等の剤型
で実用されており、これを経口経路で用いて殺虫を行な
う食毒剤としての応用は未だ実用されていない。
Furthermore, as the insecticidal components of currently known poison baits, only certain organophosphorus-based or carbamate-based insecticides are used, and pyrethroid-based insecticides are generally not used. In other words, pyrethroid insecticides are generally known to act rapidly against adult flies (hereinafter simply referred to as flies) and have excellent knockdown efficacy; It has the property of entering the body through the portal and acting extremely quickly on the nervous system, and therefore its application is limited to the respiratory route of the spiracles and the skin contact route. Pyrethroid insecticides are effective against not only flies but also mosquitoes and cockroaches due to the above properties, such as mosquito coils (air route), electric mosquito mats (same as above), aerosols (air gate route and contact route), It has been put into practical use in the form of smoke and transpiration agents (same as above), but it has not yet been put to practical use as a food poison for killing insects through the oral route.

ピレスロイド系殺虫剤を経口経路で用いて殺虫を行なう
試みとしては、例えばケイデング(J。
Attempts to kill insects using pyrethroid insecticides via the oral route include, for example, Kaedeng (J.

Keiding>の報告([)anish pest 
InfectionL aboratory Annu
al Report、 1978 。
Keiding>'s report ([)anish pest
Infection Laboratory Annu
al Report, 1978.

”Pa1nt−on−baits ” 1−abora
tory tests )があるが、この報告ではピレ
スロイド系殺虫剤を用いた毒餌を検討したが満足な結果
、は得られなかったとしている。この報告結果は、ピレ
スロイド系殺虫剤が、昆虫に対して摂食忌避作用を持つ
という一般学術情報からみれば当然のことであろう。
“Pa1nt-on-baits” 1-abora
However, this report states that poison baits using pyrethroid insecticides were investigated, but satisfactory results were not obtained. This reported result is not surprising given the general academic information that pyrethroid insecticides have a feeding repellent effect on insects.

更に近年、ピレスロイド系殺虫剤の一種である2゜2−
ジメチル−3−(β、β−ジクロロビニル)−シクロプ
ロパンカルボン酸 α−シアノ−3−フェノキシ−4−
フルオロベンピンが、ハエの毒餌に有効である旨の報告
がなされている(特開昭59−78111号公報参照)
が、この報告では上記化合物のみが有効であるとされて
おり、他のピレスロイド系殺虫剤では毒餌として不適で
あると記載されている。このように現在ピレスロイド系
殺虫剤が昆虫に忌避作用を持つこと、その経口摂取では
効力が劣ることは、当業界で一般常識となっている。
Furthermore, in recent years, 2゜2-, a type of pyrethroid insecticide, has been introduced.
Dimethyl-3-(β,β-dichlorovinyl)-cyclopropanecarboxylic acid α-cyano-3-phenoxy-4-
It has been reported that fluorobenpine is effective as a poison bait for flies (see Japanese Patent Application Laid-open No. 78111/1983).
However, this report states that only the above compound is effective, and that other pyrethroid insecticides are unsuitable as poison bait. Thus, it is now common knowledge in the industry that pyrethroid insecticides have a repellent effect on insects, and that their efficacy is inferior when taken orally.

しかし、一般にピレスロイド殺虫剤は、人畜に対して安
全性が高く、殺虫活性も高いと言われており、また害虫
の抵抗性も発達し難い殺虫剤でおることから、ハエに対
してのピレスロイド系殺虫剤の適用は重要な課題であり
、且つ毒餌剤への適用も重大な課題であった。
However, in general, pyrethroid insecticides are said to be highly safe for humans and livestock, and have high insecticidal activity, and they are also insecticides that do not easily develop resistance in pests. The application of insecticides was an important issue, and the application of poison baits was also a serious issue.

問題点を解決するための手段 本発明者は、斯かる現状に鑑み、ハエに有効な殺虫剤組
成物の開発を続けるうち、多くのピレスロイド系化合物
の中でも特に(5−ベンジル−3−フリル)メチル d
−シス/トランス−クリサンテマート、3−フェノキシ
ベンジル d−シス/トランス−クリサンプマー1〜又
は3−フェノキシベンジル dl−シス/トランス−3
−(2゜2−ジクロロビニル)−2,2−ジメチル−1
−シクロプロパンカルボキシレートが、殺虫効力発現に
充分な時間ハエを引きつけておくことができる作用を有
し、しかもハエに対する殺虫効果も強力であり抵抗性を
有するハエ、感受性を有するハエのいか/υを問わず少
量の使用で有効に駆除できることを見出した。斯かるχ
0児に基づき更に研究を重ねた結果、上記殺虫成分とハ
エの性誘引物質とを供用した場合には、ハエの誘引効果
を増強できる結果上記殺虫成分の使用量をより一層少な
くしても充分な殺虫効果を発現し得ることを見出した。
Means for Solving the Problems In view of the current situation, the present inventors continued to develop insecticide compositions effective against flies, and among many pyrethroid compounds, (5-benzyl-3-furyl) was developed. methyl d
-cis/trans-chrysanthemate, 3-phenoxybenzyl d-cis/trans-chrysampmer 1- or 3-phenoxybenzyl dl-cis/trans-3
-(2゜2-dichlorovinyl)-2,2-dimethyl-1
- Cyclopropane carboxylate has the effect of attracting flies for a sufficient period of time to develop its insecticidal effect, and has a strong insecticidal effect on flies, and has a strong insecticidal effect on flies that are resistant and susceptible. We have found that it can be effectively exterminated by using a small amount regardless of the species. Such χ
As a result of further research based on 0 children, it was found that when the above insecticidal ingredient and a fly sexual attractant were used together, the fly attracting effect could be enhanced. It has been found that this method can exhibit a significant insecticidal effect.

本発明は、斯かる知見に基づき完成されたものでおる。The present invention has been completed based on this knowledge.

即ら本発明は、(5−ベンジル−3−フリル)メチル 
d−シス/トランメーク1ノザンテマート、3−フェノ
キシベンジル d−シス/l〜ランスークリザンテマー
ト及び3−フエノギシベンジルd9−シス/トランス−
3−(2,2−ジクロロビニル>72.2−ジメチル−
1−シクロプロパンカルボキシレートからなる群より選
ばれた少なくとも1種並びに9−トリコセン、シス−9
−ト1ノコセン、10−メチル−9−トリコセン、シス
−2−メチル−8−ドコセン、シス−9−ドコセン、シ
ス−8−ドコセン及びシス−10−トリコセンからなる
群よりj穴ばれた少なくとも1種の性誘引物質を有効成
分として含有することを特徴とするハエ用誘引殺虫剤組
成物に係る。
That is, the present invention provides (5-benzyl-3-furyl)methyl
d-cis/tranmake 1 nozantemate, 3-phenoxybenzyl d-cis/l~lansu chrysanthemate and 3-phenogysibenzyl d9-cis/trans-
3-(2,2-dichlorovinyl>72.2-dimethyl-
At least one member selected from the group consisting of 1-cyclopropanecarboxylate and 9-tricosene, cis-9
- at least one hole from the group consisting of -1-nocosene, 10-methyl-9-tricosene, cis-2-methyl-8-docosene, cis-9-docosene, cis-8-docosene, and cis-10-tricosene; The present invention relates to a fly attractant and insecticide composition containing a species sexual attractant as an active ingredient.

本発明において、(5−ベンジル−3−フリル)メチル
 d−シス/トランス−クリ4ノ゛ンテマート、3−フ
ェノキシベンジル d−シス/トランス−クリυンテマ
ート及び3−フェノキシベンジルdl−シス/1〜ラン
ス−3−(2,2−ジクロロビニル)−2,2−ジメチ
ル−1−シクロプロパンカルボキシレートからなる群よ
り選ばれた少なくとも1種と上記性誘引物質との使用割
合としては、特に制限がなく広い範囲内から適宜選択す
ることか可能でおるが、通常前者1重量部に対して後者
を0.001〜1重量部程度、好ましくは0.005〜
0.5重量部程度とするのがよい。
In the present invention, (5-benzyl-3-furyl)methyl d-cis/trans-clintemate, 3-phenoxybenzyl d-cis/trans-clintemate and 3-phenoxybenzyl dl-cis/1- There are no particular restrictions on the proportion of at least one selected from the group consisting of lance-3-(2,2-dichlorovinyl)-2,2-dimethyl-1-cyclopropanecarboxylate and the above sex attractant. Although it is possible to appropriately select from a wide range, the latter is usually about 0.001 to 1 part by weight, preferably 0.005 to 1 part by weight, per 1 part by weight of the former.
The amount is preferably about 0.5 parts by weight.

本発明の組成物は、上記有効成分化合物をそのままハエ
の防除が要求される区域等に適用することもできるが、
通常好ましくは適当な担体その他の配合剤を用いて適用
区域、適用方法等に適した各種の形態例えば液剤、固剤
等に調製して利用される。
In the composition of the present invention, the above-mentioned active ingredient compound can be applied as it is to areas where fly control is required, but
Usually, it is preferably used by preparing various forms such as liquids, solids, etc., suitable for the application area, application method, etc., using appropriate carriers and other compounding agents.

液剤の形態に調製するに当り用いられる担体としては例
えばメチルアルコール、エチルアルコール等のアルコー
ル類、アセトン、メチルエチルケトン等のケトン類、テ
トラヒドロフラン、ジオキサン等のエーテル類、ヘキサ
ジ、ケロシン、パラフィン、石油ベンジン等の脂肪族炭
化水素類、ベンゼン、トルエン等の芳香族炭化水素類、
酢酸エチル等のエステル類、ジクロロエタン等のハロゲ
ン化炭化水素類等を側糸できる。これら液剤形態の本発
明組成物には、更に通常の塗膜形成剤、乳化剤、分散剤
、展着剤、湿潤剤、安定剤、噴射剤等の添加剤を配合す
ることができ、塗料形態、接着剤形態、乳剤、分散剤、
懸濁剤、ローション、クリーム、噴射剤、エアゾール剤
等の形態で利用することができる。これらの添加剤とし
ては、例えばニトロセルロース、アセチルセルロース、
アセチルブチリルセルロース、メチルセルロース等のセ
ルロース誘導体、酢酸ビニル樹脂等のビニル系樹脂、ア
ルキッド系樹脂、エチレン−酢酸ビニル(H脂、ユリア
系樹脂、エポキシ系樹脂、ポリエステル系樹脂、ウレタ
ン系樹脂、シリコン系樹脂、アクリル系樹脂、塩化ゴム
、ポリビニルアルコール等の塗膜形成剤、石鹸類、ポリ
オキシエチレンオレイルエーテル等のポリオキシエチレ
ン脂肪アルコールエステル、ポリオキシエチレンノニル
フ工二ルエーテル等のポリオキシエチレンアルキルアリ
ルエーテル、ポリオキシエチレン脂肪酸エステル、脂肪
酸グリセリド、ソルビタン脂肪酸エステル、高級アルコ
ールの硫酸エステル、ドデシルベンゼンスルホン酸ソー
ダ等のフルキルアリルスルホン酸塩等の界面活性剤、液
化石油ガス、ジメチルエーテル、フルオロカーボン等の
噴射剤、カゼイン、ピラチン、アルギン酸、CMC等を
例示できる。
Examples of carriers used in preparing liquid preparations include alcohols such as methyl alcohol and ethyl alcohol, ketones such as acetone and methyl ethyl ketone, ethers such as tetrahydrofuran and dioxane, hexadi, kerosene, paraffin, and petroleum benzine. Aliphatic hydrocarbons, aromatic hydrocarbons such as benzene and toluene,
Esters such as ethyl acetate, halogenated hydrocarbons such as dichloroethane, etc. can be used as side threads. These compositions of the present invention in liquid form can further contain additives such as conventional film forming agents, emulsifiers, dispersants, spreading agents, wetting agents, stabilizers, propellants, etc. Adhesive form, emulsion, dispersant,
It can be used in the form of suspensions, lotions, creams, propellants, aerosols, etc. These additives include, for example, nitrocellulose, acetylcellulose,
Cellulose derivatives such as acetyl butyryl cellulose and methyl cellulose, vinyl resins such as vinyl acetate resin, alkyd resins, ethylene-vinyl acetate (H fat, urea resins, epoxy resins, polyester resins, urethane resins, silicone resins) Resins, acrylic resins, chlorinated rubber, film forming agents such as polyvinyl alcohol, soaps, polyoxyethylene fatty alcohol esters such as polyoxyethylene oleyl ether, polyoxyethylene alkyl allyls such as polyoxyethylene nonyl phenyl ether, etc. Injection of surfactants such as ether, polyoxyethylene fatty acid ester, fatty acid glyceride, sorbitan fatty acid ester, sulfuric acid ester of higher alcohol, flukylaryl sulfonate such as sodium dodecylbenzenesulfonate, liquefied petroleum gas, dimethyl ether, fluorocarbon, etc. Examples include casein, piratin, alginic acid, and CMC.

また固剤の形態に調製するに当り用いられる担体として
は、例えばケイ酸、カオリン、活性炭、ベントナイト、
珪藻土、タルク、クレー、炭酸カルシウム、@磁器粉等
の鉱物質粉末、木粉、大豆粉、小麦粉、澱粉等の植物質
粉末、砂糖、シクロデキストリン等の包接化合物等を例
示できる。
In addition, examples of carriers used for preparation in solid form include silicic acid, kaolin, activated carbon, bentonite,
Examples include mineral powders such as diatomaceous earth, talc, clay, calcium carbonate, and porcelain powder, vegetable powders such as wood flour, soybean flour, wheat flour, and starch, and clathrate compounds such as sugar and cyclodextrin.

また本発明の組成物は、例えばポリビニルアルコールや
CMC等を用いたスプレードライ法、ゼラチン、ポリビ
ニルアルコール、アルギン酸等を用いた液中硬化法、コ
アセルベーション法等に従いマイクロカプセル化した形
態に調製することもできる。
Furthermore, the composition of the present invention can be prepared in a microencapsulated form by, for example, a spray drying method using polyvinyl alcohol, CMC, etc., an in-liquid curing method using gelatin, polyvinyl alcohol, alginic acid, etc., a coacervation method, etc. You can also do that.

更に本発明の組成物には、公知の摂食誘引物質、効力増
強剤、酸化防止剤、分解防止剤、殺菌剤、防黴剤、肥料
、着香剤、着色料等を配合することができる。配合可能
な摂食誘引物質としては、例えば粉乳、卵粉、サナギ粉
、オキアミ粉、食肉エキス、果汁、アルブミン、グロブ
ミン、ペプチド、アミノ酸(例えばプロリン)、カラメ
ル、麦芽エキス、ワニリン、ボエイ、穀粉、酵母、脂肪
族ラフトーン、ブドウ糖、蔗糖、麦芽糖、単糖類、三糖
類等やこれらの蛋白質もしくは炭水化物を含有する物質
等を例示できる。効力増強剤としては、例えばN−(2
−エチルヘキシル)−ビシクロ−(2,2,1)−5−
へブテン−2,3−ジカルボキシイミド、6−(プロピ
ルビペロニル)−ブチルカルビヂルエーテル、N−(2
−エチルヘキシル)−1−イソプロピル−4−メヂルビ
シクロ(2,2,2)オクト−5−エン−2,3−ジカ
ルボキシイミド等を例示できる。酸化防止剤としては、
例えばブチルヒドロキシアニソール、ジブチルヒト[1
キシトルエン、トコフェロール、γ−オリザノール等を
例示できる。分解防止剤としては、例えばフェニルグリ
シジルエーテル等を例示できる。殺菌剤としては、例え
ば゛す゛リチル酸、安息香酸、ソルビン酸、・p−クロ
ロ−m−キシレノール、2− (4’−チアゾイル)ベ
ンズイミダゾール等を例示できる。また防黴剤としては
、例えばα−ブロモシンナミックアルデヒド、N−ジメ
チル−N−フェニル−N’−(フルオロジクロロメチル
)チオスルファミド等を例示できる。
Furthermore, the composition of the present invention may contain known feeding attractants, potency enhancers, antioxidants, decomposition inhibitors, bactericides, fungicides, fertilizers, flavoring agents, coloring agents, and the like. . Examples of feeding attractants that can be blended include powdered milk, egg powder, pupa powder, krill powder, meat extract, fruit juice, albumin, globumin, peptides, amino acids (e.g. proline), caramel, malt extract, vanillin, boei, grain flour, Examples include yeast, aliphatic roughtone, glucose, sucrose, maltose, monosaccharides, trisaccharides, and substances containing these proteins or carbohydrates. As a potency enhancer, for example, N-(2
-ethylhexyl)-bicyclo-(2,2,1)-5-
Hebutene-2,3-dicarboximide, 6-(propylbiperonyl)-butylcarbidyl ether, N-(2
-ethylhexyl)-1-isopropyl-4-methylbicyclo(2,2,2)oct-5-ene-2,3-dicarboximide. As an antioxidant,
For example, butylhydroxyanisole, dibutylhuman [1
Examples include xytoluene, tocopherol, and γ-oryzanol. Examples of the decomposition inhibitor include phenyl glycidyl ether. Examples of the disinfectant include dithilylic acid, benzoic acid, sorbic acid, p-chloro-m-xylenol, and 2-(4'-thiazoyl)benzimidazole. Examples of the antifungal agent include α-bromocinnamic aldehyde, N-dimethyl-N-phenyl-N'-(fluorodichloromethyl)thiosulfamide, and the like.

斯くして調製される各種形態を有する本発明の組成物を
使用するに際しては、例えばハエの発生区域、例えば農
作物栽培畑、果樹園、温室、ビニールハウス、畜鶏舎、
穀物金庫、食堂の厨房、一般家庭等に本発明組成物を載
置、散布、噴霧、塗布、張り付は等すればよい。本発明
における駆除対象となるハエの種類としては、特に限定
がなく、例えばイエバエ科(イエバエ、オオイエバエ、
サシバエ、ヒメクロバエ等)、ヒメイエバエPI (ヒ
メイエバエ等)、クロバエ科(オオクロバエ、ケブカク
ロバエ、ヒツジキンバエ、ヒツジキンバエ、キンバエ、
ミドリキンバエ、オビキンバエ、クロバエ等)、ニクバ
エ科(センチニクバエ、ナミニクバエ等)、ショウジョ
バエ科(キイロショウジョバエ、クロショウジョバエ等
)、チーズバエ科(チーズバエ等)、フンバエ!Sl 
(ヒメフンバエ等)、ベラコラバエ+=t、 <ベラコ
ラバエ等)、ノミバエ科(ノミバエ等)等いずれのハエ
に対しても有効である。
When using the composition of the present invention having various forms prepared in this manner, for example, fly infested areas such as crop cultivation fields, orchards, greenhouses, greenhouses, poultry houses,
The composition of the present invention may be placed, scattered, sprayed, coated, and pasted in grain safes, cafeteria kitchens, general households, and the like. The types of flies to be exterminated in the present invention are not particularly limited.
Stable flies, Common black flies, etc.), Common blow flies PI (Japanese common flies, etc.), Black fly families (Great blow flies, Common blow flies, Common black flies, Common black flies, Common black flies, Common blow flies,
Green fruit flies, black flies, black flies, etc.), Drosophilidae (sentinic flies, black flies, etc.), Drosophilidae (drosophila melanogaster, black fruit flies, etc.), Cheese flies (cheese flies, etc.), and dung flies! Sl
It is effective against any of the flies such as (Flea fly, etc.);

本発明組成物中に含有されるべき(5−ベンジル−3−
フリル)メチル d−シス/トランス−クリサンテマー
ト等及び上記性誘引物質(以下これらを総称して「有効
成分化合物」という)の品並びに本発明組成物の適用量
としては、その剤型や適用方法、適用場所等に応じて適
宜に決定ずればよく、特に限定されるものではない。例
えば分散剤ヤ水和剤等の液剤の形態で用いる場合には、
液剤中に有効成分化合物を通常1〜25重量%程度、好
ましくは5〜15重量%程度配合しておくのがよく、粉
剤等の固剤の形態で用いる場合には、固剤中に有効成分
化合物を通常0.1〜15重凹%程度、好ましくは0.
3〜4重量%程度配合しておくのがよい。またその適用
mとしては、例えば塗布使用の場合、塗布すべき面積1
cm2当りに有効成分化合物を通常0.01m(]以上
、好ましくは0.05〜0.1mg程度とするのがよく
、固剤その他の形態で用いる場合、敗イ[面積1m2当
り有効成分化合物を通常1mg以上、好ましくは3〜1
0mg程度とするのがよい。
(5-benzyl-3-
Furyl) methyl d-cis/trans-chrysanthemate, etc. and the above-mentioned sex attractants (hereinafter collectively referred to as "active ingredient compounds") and the amount of the composition of the present invention to be applied will depend on its dosage form and application. It may be determined as appropriate depending on the method, application location, etc., and is not particularly limited. For example, when used in the form of a liquid such as a dispersant or a hydrating powder,
It is best to mix the active ingredient compound in the liquid formulation in an amount of about 1 to 25% by weight, preferably about 5 to 15% by weight, and when using it in the form of a solid such as a powder, the active ingredient in the solid The compound is usually about 0.1 to 15%, preferably 0.1% to 15%.
It is preferable to add about 3 to 4% by weight. In addition, as the application m, for example, in the case of coating use, the area to be coated is 1
The amount of active ingredient compound per cm2 is usually 0.01 m () or more, preferably about 0.05 to 0.1 mg. Usually 1 mg or more, preferably 3 to 1
It is best to set the amount to about 0 mg.

発明の効果 本発明の組成物は、殺虫効力発現に充分な時間ハエを引
きつけておくことができる作用を有し、しかもハエに対
する殺虫効果も強力であり、従って本発明組成物を使用
すれば、抵抗性を有するハエ、感受性を有するハエのい
かんを問わず少量の使用で有効に駆除することができる
Effects of the Invention The composition of the present invention has the ability to attract flies for a sufficient period of time to develop its insecticidal effect, and has a strong insecticidal effect on flies. Therefore, if the composition of the present invention is used, Both resistant and susceptible flies can be effectively exterminated by using a small amount.

実施例 以下に製剤例及び試験例を掲げて本発明をより一層明ら
かにηる。尚、単に「部」とあるのは「重量品」を意味
する。
EXAMPLES The present invention will be explained more clearly by presenting formulation examples and test examples below. Note that "part" simply means "heavy item".

製剤例1 (粉剤) (5−ベンジル−3−フリル)メチル d−シス/トラ
ンス−クリサンナマー1〜(以下「化合物A」という〉
2部にシス−9−トリコセン1部を加え、これをアセト
ンに溶解し、次いで300メツシュタルク97部を加え
て充分に撹拌した後、アセトンを除去し、本発明の粉剤
を1qた。
Formulation Example 1 (Powder) (5-benzyl-3-furyl)methyl d-cis/trans-chrysannamer 1~ (hereinafter referred to as "Compound A")
1 part of cis-9-tricosene was added to 2 parts, and this was dissolved in acetone. Then, 97 parts of 300 Metsstarck were added and thoroughly stirred, and the acetone was removed to obtain 1 q of the powder of the present invention.

製剤例2 (乳剤) 化合物A5部にシス−9−トリコセン0.1部を加え、
次にキシレン60部及びツルボール〔界面活性剤〕35
部を順次加えて混合、fj2拝して本発明の乳剤を得た
Formulation Example 2 (Emulsion) Add 0.1 part of cis-9-tricosene to 5 parts of Compound A,
Next, 60 parts of xylene and 35 parts of Tsurubol [surfactant]
The emulsion of the present invention was obtained by sequentially adding 1 part to the mixture, mixing, and repeating fj2.

製剤例3 (乳剤) 化合物A’IO部にシス−9−トリコセン0.3部を加
え、次にキシレン60部及びツルポール30部を順次加
えて混合、撹拌して本発明の乳剤を1qだ。
Formulation Example 3 (Emulsion) 0.3 parts of cis-9-tricosene was added to compound A'IO, and then 60 parts of xylene and 30 parts of Tulpol were sequentially added and mixed and stirred to prepare 1 q of the emulsion of the present invention.

製剤例4 (乳剤) 化合物A20部にシス−9−トリコセン1部を加え、次
にキシレン60部及びツルポール20部を順次加えて混
合、撹拌して本発明の乳剤を得た。
Formulation Example 4 (Emulsion) 1 part of cis-9-tricosene was added to 20 parts of Compound A, and then 60 parts of xylene and 20 parts of Trupol were sequentially added, mixed and stirred to obtain an emulsion of the present invention.

製剤例5 (乳剤) 化合物A20部にシス−9−トリコセン1部を加え、次
にキシレン60部及びポリスキシエチレンスチレン化フ
ェニルエーテルポリマー(界面活性剤)20部を順次加
えて混合、撹拌して本発明の乳剤を19だ。
Formulation Example 5 (Emulsion) 1 part of cis-9-tricosene was added to 20 parts of Compound A, and then 60 parts of xylene and 20 parts of polyoxyethylene styrenated phenyl ether polymer (surfactant) were sequentially added, mixed, and stirred. The emulsion of the present invention is 19.

製剤例6 (乳剤) 化合物A20部にシス−9−トリコセン1部を加え、次
にキシレン60部、グリセロールの脂肪酸エステル15
部及びCMC5部を順次加えて混合、撹拌して本発明の
乳剤を得た。
Formulation Example 6 (Emulsion) Add 1 part of cis-9-tricosene to 20 parts of Compound A, then add 60 parts of xylene and 15 parts of fatty acid ester of glycerol.
1 part and 5 parts of CMC were sequentially added, mixed and stirred to obtain an emulsion of the present invention.

製剤例7 (乳剤) 化合物A20部にシス−9−トリコセン1部を加え、次
にキシレン60部、パラフィンスルホン酸〔界面活性剤
320部及び力1122部を順次加えて混合、撹拌して
本発明の乳剤を1qた。
Formulation Example 7 (Emulsion) 1 part of cis-9-tricosene was added to 20 parts of Compound A, and then 60 parts of xylene, 320 parts of paraffin sulfonic acid [320 parts of surfactant, and 1122 parts of force] were sequentially added, mixed, and stirred to prepare the present invention. 1 q of emulsion.

製剤例8 (水和剤) 化合物A20部にシス−9−トリコセン0.1部を加え
、次にツルポール5部を加えて混合し、更にホワイトカ
ーボン55部を加え、捕漬器中にて充分撹拌、混合して
本発明の水和剤を得た。
Formulation Example 8 (Wettable powder) Add 0.1 part of cis-9-tricosene to 20 parts of Compound A, then add 5 parts of Tsurpol and mix, then add 55 parts of white carbon and stir thoroughly in a trap. , and mixed to obtain the hydrating agent of the present invention.

製剤例9 (油剤) 化合物A5部及びシス−9−トリコ廿ン0.1部をケロ
シン90部に溶解して本発明の油剤を得た。
Formulation Example 9 (Oil agent) An oil agent of the present invention was obtained by dissolving 5 parts of Compound A and 0.1 part of cis-9-tricone in 90 parts of kerosene.

製剤例10  (油剤) 化合物A5部及び9−トリコセン0.1部を灯irb 
90部に溶解して本発明の油剤を得た。
Formulation Example 10 (Oil) 5 parts of Compound A and 0.1 part of 9-tricosene were heated under irb.
The oil agent of the present invention was obtained by dissolving in 90 parts.

製剤例11 (油剤) 化合物A10部及び9−トリコレン0.5部をケロシン
90部に溶解して本発明の油剤を得た。
Formulation Example 11 (Oil agent) An oil agent of the present invention was obtained by dissolving 10 parts of Compound A and 0.5 parts of 9-tricholene in 90 parts of kerosene.

製剤例12 (エアゾール) 化合物A1部、シス−9−トリコセン0.05部及び脱
臭灯油3部を混合溶解し、エアゾール容器に充填し、バ
ルブ部分を取付けた後、該バルブ部分を通じて液化石油
ガス85部を加圧充填することにより本発明のエアゾー
ルを得た。
Formulation Example 12 (Aerosol) 1 part of Compound A, 0.05 part of cis-9-tricosene, and 3 parts of deodorized kerosene are mixed and dissolved, filled into an aerosol container, and a valve part is attached. After that, 85 parts of liquefied petroleum gas is injected through the valve part. The aerosol of the present invention was obtained by pressurizing and filling the sample.

製剤例13 (微粒剤) 化合物A2部及びシス−9−トリコセン0.01部を微
粒ベントナイト96.5部に吸着させ、ナウターミキザ
ーで20分間混合した。更にカープレックス1部を加え
て15分間混合し、本発明の微粒剤を1qだ。
Formulation Example 13 (Fine Granules) 2 parts of Compound A and 0.01 part of cis-9-tricosene were adsorbed onto 96.5 parts of fine bentonite, and mixed for 20 minutes using a Nauta mixer. Further, 1 part of Carplex was added and mixed for 15 minutes, and 1 q of the microgranules of the present invention were added.

試験例 製剤例2で1qられた乳剤を100倍に希釈し、これを
木製プレートにスプレーし、該プレー1〜を畜舎内に設
置した。1日後該プレートの周囲に死亡しているハエの
数を調べた。この試験を3回繰返した。その結果、平均
46匹のハエの死亡を確認した。
Test Example 1 q of the emulsion prepared in Preparation Example 2 was diluted 100 times, and this was sprayed onto a wooden plate, and the plates 1 to 1 were placed in a livestock barn. One day later, the number of dead flies around the plate was determined. This test was repeated three times. As a result, it was confirmed that an average of 46 flies died.

製剤例13で4H,1られだ微粒剤10gをプラスチッ
ク容器にいれ、ハエの発生した場所に設置した。
In Formulation Example 13, 10 g of the 4H,1 Radar microgranules were placed in a plastic container and placed in a place where flies were infested.

1日後該容器内及びその周囲に死亡しているハエの数を
調べた。この試験を3回繰返した°。その結果、平均6
6匹のハエの死亡を確認した。
One day later, the number of dead flies in and around the container was examined. This test was repeated three times. As a result, the average
Six flies were confirmed dead.

(以 上) ・、−ゴ/ 一ロれ(that's all) ・、-go/ One roll

Claims (1)

【特許請求の範囲】 [1](5−ベンジル−3−フリル)メチル d−シス
/トランス−クリサンテマート、3−フェノキシベンジ
ル d−シス/トランス−クリサンテマート及び3−フ
ェノキシベンジル dl−シス/トランス−3−(2,
2−ジクロロビニル)−2,2−ジメチル−1−シクロ
プロパンカルボキシレートからなる群より選ばれた少な
くとも1種、並びに 9−トリコセン、シス−9−トリコセン、10−メチル
−9−トリコセン、シス−2−メチル−8−ドコセン、
シス−9−ドコセン、シス−8−ドコセン及びシス−1
0−トリコセンからなる群より選ばれた少なくとも1種
の性誘引物質 を有効成分として含有することを特徴とするハエ用誘引
殺虫剤組成物。
[Scope of Claims] [1] (5-Benzyl-3-furyl)methyl d-cis/trans-chrysanthemate, 3-phenoxybenzyl d-cis/trans-chrysanthemate and 3-phenoxybenzyl dl-cis /trans-3-(2,
At least one member selected from the group consisting of (2-dichlorovinyl)-2,2-dimethyl-1-cyclopropanecarboxylate, as well as 9-tricosene, cis-9-tricosene, 10-methyl-9-tricosene, cis- 2-methyl-8-docosene,
cis-9-docosene, cis-8-docosene and cis-1
1. A fly attractant and insecticide composition containing as an active ingredient at least one sex attractant selected from the group consisting of O-tricosene.
JP60166359A 1985-07-18 1985-07-26 Attractant and insecticidal composition for fly Granted JPS6226208A (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
JP60166359A JPS6226208A (en) 1985-07-26 1985-07-26 Attractant and insecticidal composition for fly
BR8606797A BR8606797A (en) 1985-07-18 1986-07-18 FLY ATTRACTION COMPOSITION
EP86904389A EP0229191B1 (en) 1985-07-18 1986-07-18 Fly-attractive composition
PCT/JP1986/000373 WO1987000401A1 (en) 1985-07-18 1986-07-18 Fly-attractive composition
KR1019870700238A KR940000802B1 (en) 1985-07-18 1986-07-18 Composition for attracting flies
DE86904389T DE3688525T2 (en) 1985-07-18 1986-07-18 FLY ATTRACTION COMPOSITION.
AU61368/86A AU591161B2 (en) 1985-07-18 1986-07-18 Fly-attractive composition
US07/031,068 US4855133A (en) 1985-07-18 1986-07-18 Composition for attracting flies

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60166359A JPS6226208A (en) 1985-07-26 1985-07-26 Attractant and insecticidal composition for fly

Publications (2)

Publication Number Publication Date
JPS6226208A true JPS6226208A (en) 1987-02-04
JPH0560441B2 JPH0560441B2 (en) 1993-09-02

Family

ID=15829924

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60166359A Granted JPS6226208A (en) 1985-07-18 1985-07-26 Attractant and insecticidal composition for fly

Country Status (1)

Country Link
JP (1) JPS6226208A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5925367A (en) * 1988-12-28 1999-07-20 Ciba-Geigy Corporation Pest control with UV blockers and pheromones
JP2011153130A (en) * 2009-12-28 2011-08-11 Sumitomo Chemical Co Ltd Fly-attracting agent and fly-attracting method, and fly-exterminating agent and fly-exterminating method
JP2013151470A (en) * 2011-12-28 2013-08-08 Dainippon Jochugiku Co Ltd Flying insect pest attracting agent
JP2019517534A (en) * 2016-05-30 2019-06-24 グローバケム エンフェー Use of 9-trichocene for the control of Drosophila SUZUK II

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5925367A (en) * 1988-12-28 1999-07-20 Ciba-Geigy Corporation Pest control with UV blockers and pheromones
JP2011153130A (en) * 2009-12-28 2011-08-11 Sumitomo Chemical Co Ltd Fly-attracting agent and fly-attracting method, and fly-exterminating agent and fly-exterminating method
US9867374B2 (en) 2009-12-28 2018-01-16 Sumitomo Chemical Company, Limited Fly attractant composition and fly attracting method, as well as fly expellant composition and fly expelling method
JP2013151470A (en) * 2011-12-28 2013-08-08 Dainippon Jochugiku Co Ltd Flying insect pest attracting agent
JP2019517534A (en) * 2016-05-30 2019-06-24 グローバケム エンフェー Use of 9-trichocene for the control of Drosophila SUZUK II

Also Published As

Publication number Publication date
JPH0560441B2 (en) 1993-09-02

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