JPH01299203A - Termite-controlling agent for soil-treatment - Google Patents

Termite-controlling agent for soil-treatment

Info

Publication number
JPH01299203A
JPH01299203A JP63128799A JP12879988A JPH01299203A JP H01299203 A JPH01299203 A JP H01299203A JP 63128799 A JP63128799 A JP 63128799A JP 12879988 A JP12879988 A JP 12879988A JP H01299203 A JPH01299203 A JP H01299203A
Authority
JP
Japan
Prior art keywords
compound
soil
agent
termite
controlling agent
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
JP63128799A
Other languages
Japanese (ja)
Other versions
JP2610483B2 (en
Inventor
Yoshio Katsuta
純郎 勝田
Takeshi Yoshimura
剛 吉村
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.)
Dainihon Jochugiku Co Ltd
Original Assignee
Dainihon Jochugiku 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 Dainihon Jochugiku Co Ltd filed Critical Dainihon Jochugiku Co Ltd
Priority to JP63128799A priority Critical patent/JP2610483B2/en
Publication of JPH01299203A publication Critical patent/JPH01299203A/en
Application granted granted Critical
Publication of JP2610483B2 publication Critical patent/JP2610483B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE:To obtain the subject controlling agent having excellent safety to human and animal and stability in soil, by using dimethyl (4-ethoxyphenyl) {3-(3-phenoxy-4-fluorophenyl)-propyl} silane and octachlorodipropyl ether as active components. CONSTITUTION:The objective controlling agent contains the compound of formula I and octachlorodipropyl ether at a ratio of 1:(1-5). The content of the compound of formula I in the agent is 0.01-90wt.%. The agent may be incorporated with a termite attractant to improve the efficiency of termite-proofing effect or with various other insecticide (such as organophosphorus, pyrethroidal or carbamate-type insecticides), preservative, etc., to obtain a composition for multi-purpose use. The above controlling agent can be used in various form. The chemical stability of the agent can be further improved and the residual activity in the soil can be increased by the micro-encapsulation or cyclodextrin- inclusion of the compound of formula.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明はジメチ/I/(4−エトキシフェニ/L/)1
3−(3−フェノキV−4−フルオロフェニ/I/)プ
ロピ/v1シラン(以下化合物Aと称す)と、オクタク
ロロジプロピμエーテfi/(以下S−421と称す)
を含有することを特徴とする土壌処理用白アリ防除剤に
関する。
[Detailed description of the invention] [Industrial application field] The present invention relates to dimethy/I/(4-ethoxypheny/L/)1
3-(3-phenoxyV-4-fluoropheny/I/)propy/v1 silane (hereinafter referred to as compound A) and octachlorodipropyl ether fi/(hereinafter referred to as S-421)
The present invention relates to a termite control agent for soil treatment, characterized by containing the following.

〔従来の技術〕[Conventional technology]

近年、木材を食害する害虫、例えば白アリ。 In recent years, pests that damage wood, such as termites, have become popular.

フナクイムシ、とツクキクイムシ等の被害が問題となっ
ているが、これらの害虫に食害されないために、あらか
じめ用材や床下土壌に防虫剤を処理する方法が従来より
行われ、この目的のために殺虫、防虫成分としてクロル
デン、ディルドリン等の有機塩素系殺虫剤が使われてき
た。
Damage caused by crucian beetles and wood beetles has become a problem, but in order to avoid being eaten by these pests, it has traditionally been the practice to treat lumber and sub-soil with insect repellents in advance. Organochlorine insecticides such as chlordane and dieldrin have been used as insect repellent ingredients.

しかしながら、これらの殺虫、防虫成分はいずれも残留
性、毒性、刺激性、環境汚染などの点で問題があり、昨
年使用が禁止され、これらに替わるものとして、クロμ
ピリホス。
However, these insecticidal and insect repellent ingredients all have problems in terms of persistence, toxicity, irritation, and environmental pollution, and their use was banned last year.
Pyrifos.

ホキシムなどの有機リン剤が最近上布された。Organophosphorus agents such as phoxim have recently been introduced.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

上記有機リン系土壌処理用白アリ防除剤は土壌中で分解
されやすいため長期間にわたる白アリ防除効果が乏しく
、また人畜に対する安全性の点で問題が多いという欠点
があり、低毒性の新しい白アリ防除剤の開発が切望され
ている。
The organophosphorus-based termite control agent for soil treatment has the drawback that it is easily decomposed in the soil and has poor termite control effects over a long period of time, and there are many safety issues for humans and livestock. There is a strong need for the development of an ant control agent.

〔問題点を解決するための手段及び作用〕本発明者らは
、低毒性を特徴とするピレスロを長年研究してきたが、
その結果、クロルデン、デイ〃ドリンより殺虫性、残効
性において優れた化合物として化合物Aを見い出した。
[Means and effects for solving the problem] The present inventors have been researching Pirethro, which is characterized by low toxicity, for many years.
As a result, Compound A was found to be a compound superior to chlordane and deidrin in terms of insecticidal properties and residual efficacy.

化合物Aは、特にリン翅目の害虫、アブラムシ類、ウン
カ類等に高い殺虫活性を有するため農園芸用分野で実用
化が検討されているが、直翅目の害虫に対して低活性で
あることからこれまで白アリ防除剤用途には不向きであ
ると考えられていた。
Compound A is being considered for practical use in the field of agriculture and horticulture because it has high insecticidal activity against insect pests of the order Phosphoroptera, aphids, planthoppers, etc., but it has low activity against pests of the order Orthoptera. For this reason, it was thought until now that it was unsuitable for use as a termite control agent.

しかるに本発明者らは白アリの生態等を考慮した時、白
アリ防除剤の殺虫、防虫成分の評価としては基礎殺虫効
力試験のみでは不適切、lL令才勿 であると考え、種々のi社−社≠傘について実用的な木
部処理試験を行ったところ化合物Aが高い食害防止効果
を示すことが明らかとなった。化合物Aはピレスロイド
系薬剤としての特長である昆虫に対する速効性、温血動
物に対して低毒性という長所をもつと同時に非常にすぐ
れた残効性を有している。
However, when considering the ecology of termites, the present inventors believed that basic insecticidal efficacy tests alone were inappropriate and inadequate for evaluating the insecticidal and insect repellent components of termite control agents, and therefore conducted various i. When a practical wood treatment test was conducted on Sha-sha≠umbrella, it was revealed that Compound A exhibits a high effect on preventing feeding damage. Compound A has the advantages of rapid action against insects and low toxicity against warm-blooded animals, which are the characteristics of a pyrethroid drug, and at the same time has an extremely excellent residual effect.

更に本発明者らは、化合物Aが有機塩素系殺虫剤や有機
リン剤と比べると高価な殺虫剤であることを鑑み、コス
トダウンを図る目的で土壌処理用白アリ防除剤をめざし
たピレスロイド系薬剤の探索を行ったところ、化合物A
と3−421との組み合わせが、ピベロニルプトキサイ
ド、サイネピリン500 、MGK−264。
Furthermore, considering that Compound A is an expensive insecticide compared to organochlorine insecticides and organophosphorus agents, the present inventors developed a pyrethroid-based termite control agent for soil treatment in order to reduce costs. When searching for a drug, Compound A
The combination of and 3-421 is piveronyl ptoxide, cinepirin 500, and MGK-264.

セサミン、スルホキサイド、N工A−16388など、
他の共力剤に比べて特異的に高い相乗効果を示すことを
見い出し本発明を完成した 8−421を白アリ防除剤の成分として使用する知見は
例えば特開昭61−17502号公報で会知であるが、
該公報はS−421と有機リン剤ホキシムとの混合物を
趣旨としたもので、本発明が開示する化合物AとS−4
21の相乗効果を示唆するものは全くない。
Sesamin, sulfoxide, Nko A-16388, etc.
The knowledge of using 8-421, which was discovered to have a specifically high synergistic effect compared to other synergists and completed the present invention, as a component of a termite control agent was disclosed in, for example, Japanese Patent Laid-Open No. 17502/1983. I know, but
This publication is aimed at a mixture of S-421 and the organic phosphorus agent phoxim, and contains compounds A and S-4 disclosed in the present invention.
There is no suggestion of a synergistic effect of 21.

この結果、化合物Aの配合量を減らしても高い殺虫、防
虫効果を得ることが可能となり、コスト面での実用的メ
リットは版めて大きい。
As a result, it is possible to obtain high insecticidal and insect repellent effects even if the amount of compound A is reduced, and the practical advantage in terms of cost is extremely large.

本発明で用いる化合物Aは次式CI)で示され、分子中
にケイ素原子を含有している。
Compound A used in the present invention is represented by the following formula CI) and contains a silicon atom in the molecule.

土壌処理用白アリ防除剤には殺虫、防虫成分として化合
物人を0.01〜90重量%含有することができ、S−
421と混合する場合、高い共力効果を奏する化合物A
と8−421との混合比は3:1〜l二20(好壕しく
はl:l〜1:5)が適当である。
The termite control agent for soil treatment can contain 0.01 to 90% by weight of a compound as an insecticidal and insect repellent component, and S-
Compound A exhibits a high synergistic effect when mixed with 421
A suitable mixing ratio of 8-421 and 8-421 is 3:1 to 1220 (preferably 1:1 to 1:5).

また、殺虫、防虫効果をより効率的に発揮させるために
白アリ誘引剤を適宜配合してもよい。更に、本発明の土
壌処理用白アリ防除剤に、例えばクロルピリホス、ホキ
シム、ピリダフェンチオンなどの有機リン剤、7μパリ
ネート。
In addition, a termite attractant may be appropriately added in order to exhibit insecticidal and insect repellent effects more efficiently. Furthermore, the termite control agent for soil treatment of the present invention includes, for example, organic phosphorus agents such as chlorpyrifos, phoxim, and pyridafenthione, and 7μ parinate.

バーメスリン、フェンバレレート、フェンプロパスリン
などのピレスロイド剤あるいはトリプロピルイソシアヌ
レート、カーバメート剤などの他の殺虫剤、また、次に
示すような種々のタイプの防腐剤 0CCA系化合物−ccA、caBなどOハロフェノー
ル系化合物−ベンタクロ〜フェニ/L’う’7レート、
p−プロモー2.6− S)クロルフェノール Oヨードプロバルギμ系化合物−工F−1000。
Pyrethroids such as vermethrin, fenvalerate, fenpropathrin or other insecticides such as tripropylisocyanurate, carbamates, and various types of preservatives such as 0CCA-based compounds such as ccA, caB, etc. Phenolic compounds - bentacro-pheni/L'u'7 rate,
p-Promo2.6-S) Chlorphenol O iodoprobargi μ-based compound-Engineering F-1000.

3−ヨード−2−グロビニルブチルカーパメートなど 0第4級アンモニウム化合物およびアミン塩〜ベンザル
コニウムクロリド、ジアルキルジメチルアンモニウムク
ロリドなど O有機スズ化合物−ビス−(n−)!Jプチルヌズ)オ
キシド、トリブチμスズテレフタレートなど Oその他− ナフテン酸亜塩.キシリゲンアルミニウム
塩など を適宜混合して有用な多目的組成物を得ることもできる
0 Quaternary ammonium compounds and amine salts such as 3-iodo-2-glovinylbutylcarpamate to O organotin compounds such as benzalkonium chloride and dialkyldimethylammonium chloride - bis-(n-)! J Butyl Nuz) oxide, tributyl μtin terephthalate, etc. O Others - Naphthenic acid subsalts. A useful multi-purpose composition can also be obtained by appropriately mixing xyligen aluminum salt or the like.

本発明土壌処理用白アリ防除剤の剤型としては、防除剤
の性状、使用目的により、油剤、乳剤、水和剤、水溶剤
、粉剤、粒剤、エアシール剤など種々可能であるが、乳
剤、水溶剤が−収約である。いずれの製剤も常法に従っ
て調製することができ、固体担体としては粘土類(カオ
リン、ベントナイト類など)、夕tvり類などの倣わ)
末ないし粉状物があげられる。
The termite control agent for soil treatment of the present invention can be in various forms depending on the properties of the control agent and the purpose of use, such as oil, emulsion, wettable powder, aqueous solution, powder, granule, and air sealant. , the aqueous solvent is -condensing. Both preparations can be prepared according to conventional methods, and solid carriers include clays (kaolin, bentonites, etc.), night televisions, etc.)
Can be given as powder or powder.

液体担体としては、水、アルコール類、芳香族炭化水素
類(例えばトルエン、キシレンなど)。
Liquid carriers include water, alcohols, aromatic hydrocarbons (eg toluene, xylene, etc.).

脂肪族炭化水素類(例えばケロシン、灯油など)。Aliphatic hydrocarbons (e.g. kerosene, kerosene, etc.).

エステ/l/類、ニトリN1t4などが使用できる。次
に界面活性剤としてはア〜キ/L’硫酸エヌテμ類。
Esthetic/l/type, Nitori N1t4, etc. can be used. Next, as surfactants, A-K/L' sulfate NTE μ are used.

アルキルスルホン酸塩、アルキ〜アリ−yスルホン酸塩
、ポリエチレングリコ−p工−テ〃類、多価アlレコー
pエステ/L’類などがあげられる。、そのmi宜、カ
ゼイン、ゼラチン、でんぷん扮、 t、yc 。
Examples include alkyl sulfonates, alkyl-ary sulfonates, polyethylene glycol-p-esters, and polyhydric alcohol-p-esters/L's. , its composition, casein, gelatin, starch, t, yc.

ポリビニμアルコールなどの固着剤や分散剤が使用され
る。また、本発明で使用される化合物Aをマイクロカプ
セμ化あるいはサイクロデキストリン包接化することに
より、史に化学的安定性を増し土壌中における残効性を
高める製剤を得ることができる。一方、化合物人と8−
421の混合物についても上記と同様の効果が得られる
A fixing agent or dispersing agent such as polyvinyl μ alcohol is used. Further, by microcapsulating or cyclodextrin inclusion of Compound A used in the present invention, it is possible to obtain a formulation with increased chemical stability and enhanced residual efficacy in soil. On the other hand, compound people and 8-
The same effect as above can be obtained with a mixture of No. 421.

本発明の土壌処理用向アリ防除剤の適用方法としては、
従来の方法例えば家屋下や周囲の土壌に乳剤、粒剤、水
利剤、粉剤などを散布あるいは泡沫施用したり、白アリ
防除剤を含有する樹脂エマルジョンを散布して、樹脂膜
を土壌および基礎表面に形成する方法などがあげられる
The method for applying the ant control agent for soil treatment of the present invention is as follows:
Conventional methods include spraying or foaming emulsions, granules, irrigation agents, powders, etc. on the soil under and around houses, or spraying a resin emulsion containing a termite control agent to spread a resin film on the soil and foundation surfaces. For example, there are methods of forming

また前記マイクロカプセル化あるいはサイクロデキスト
リン包接化した製剤は土壌中での残効性が高められ、土
壌処理剤として有効な適用方法である。
Furthermore, the microencapsulated or cyclodextrin-encapsulated preparation has increased residual effectiveness in soil, and is an effective application method as a soil treatment agent.

〔実 施 例〕。〔Example〕.

以下本発明の有用性を一層明確にするため、実施例及び
試験例について説明するが本発明がこれらのみに限定さ
れるものでないことはもちろんである。
EXAMPLES In order to further clarify the usefulness of the present invention, Examples and Test Examples will be described below, but it goes without saying that the present invention is not limited to these.

製剤例1 化合物A5部、S−42110部にソルボ−A/5M−
200(東邦化学登録商標名)5部、キシロ−々20部
、白灯油60部を加え、これらをよくかく拌混合溶解し
て乳剤を得る。
Formulation Example 1 5 parts of Compound A, 110 parts of S-42, and Sorbo-A/5M-
200 (registered trademark of Toho Chemical), 20 parts of xylol, and 60 parts of white kerosene were added, and these were mixed and dissolved by stirring well to obtain an emulsion.

製剤例2 化合物A1部、5−4214部、ペンタクロロフェノー
ル3部に乳化剤ハイマー/vPs−AP(松本油脂11
t11薬登録商標名)20部及び精製水72部を加えて
水溶剤を得る。
Formulation Example 2 Emulsifier Hymer/vPs-AP (Matsumoto Yushi 11
Add 20 parts of t11 medicine registered trademark name) and 72 parts of purified water to obtain an aqueous solvent.

試験例1 2ケの広口ビンが円筒状の通路でつながった装置を用い
た。一方のビンには木片を、他方には無処理サンプ(ロ
ーム40gに蒸留水8dを加えたものを入れ、また、間
の通路には試験土壌(製剤例1に準じてtI4mした乳
剤の所定希釈g!12 gをサンデイローム48gに処
理後、その12gを採取)を5c1Rの距離になるよう
に詰めた。
Test Example 1 A device was used in which two wide-mouthed bottles were connected through a cylindrical passage. One bottle contains wood chips, the other contains an untreated sample (40 g of loam mixed with 8 d of distilled water), and the passageway between them contains test soil (prescribed dilution of emulsion with a tI of 4 m according to Formulation Example 1). g!12 g was processed into 48 g of Sunday loam, and 12 g of it was collected) and packed to a distance of 5c1R.

無処理サンデイロームを含むビンにイエシロアリ職蟻2
00頭及び兵蟻20頭を投入し、21日後の試験土壌の
貫通度を調べたところ次の如くであった。
2 house termite worker ants in a jar containing untreated Sunday loam
00 and 20 soldier ants were introduced, and the degree of penetration of the test soil after 21 days was examined, and the results were as follows.

なお、いずれも化合物Aの供試濃度は0.5%としたう 土壌処理試験の結果、化合物Aと8−421の組み合わ
せが特異的に相乗効果を示し、一方、ピベロニルプトキ
サイド、サイネピリン500など他の共力剤については
効果のレベルは低かった。
In addition, as a result of a soil treatment test in which the test concentration of Compound A was 0.5% in both cases, the combination of Compound A and 8-421 showed a specific synergistic effect, while piveronyl ptoxide, Other synergists, such as cinepirin 500, had lower levels of efficacy.

ヤマトシロアリについても同様の傾向が得られた。A similar trend was observed for Yamato termites.

相乗効果の理由に関しては不明な点が多いが、S−42
1の忌避効果が化合物Aの殺蟻効力に大きく関与してい
るものと考えられる。
Although there are many unknowns regarding the reason for the synergistic effect, S-42
It is considered that the repellent effect of Compound A is largely involved in the anticide effect of Compound A.

試験例2 試験例1に準じて下記の供試乳剤を用いて土壌処理試験
を行ったところ以下の如くであった。
Test Example 2 A soil treatment test was conducted using the following sample emulsion according to Test Example 1, and the results were as follows.

試験の結果、貫通度が10mm以下が合格という基準か
ら判断すると化合物Aの濃度が0.5%の場合、化合物
Aと3−421の混合比が1:1〜1:2.化合物への
濃度が0,25%の場合1:1〜1:10で十分な効果
が得られた。
As a result of the test, judging from the standard that a penetration degree of 10 mm or less is acceptable, when the concentration of Compound A is 0.5%, the mixing ratio of Compound A and 3-421 is 1:1 to 1:2. When the concentration of the compound was 0.25%, a sufficient effect was obtained at a ratio of 1:1 to 1:10.

製剤上あるいはコスト面からみて1:1〜1:5が実用
的と思われる。
From the standpoint of formulation or cost, a ratio of 1:1 to 1:5 seems to be practical.

実施例1 化合物A5部、S−4218部、フルパリネート5部に
5M−200(J[邦化学登録商標名)10部、キシロ
−1′v15部及び白灯油57部を加えてこれらをよく
かく拌混合溶解して乳剤を得る。
Example 1 To 5 parts of Compound A, 18 parts of S-42, and 5 parts of fluparinate, 10 parts of 5M-200 (J [Japanese chemical registered trademark name), 15 parts of Xylo-1'v, and 57 parts of white kerosene were added, and these were stirred well. Mix and dissolve to obtain an emulsion.

この乳剤の水rこよる30倍希釈液を、床下に設置され
ている架台類の周囲20crx巾の土壌部分、浴室、便
所、玄関、勝手口などの土間コンクリート下の土壌部分
、地中から立ち上がる自己管類の周囲20c渭巾の土壌
部分などに、1rlあたり31の割合で動力噴霧機を用
いて散布したところ、5年間にわたって白アリの食害を
防止できた。
A 30 times diluted solution of this emulsion with water is applied to the soil area of 20crx width around the frames installed under the floor, the soil area under the concrete floor of bathrooms, toilets, entrances, back entrances, etc., and the soil area that rises from the ground. When sprayed using a power sprayer at a rate of 31 ml per 1 rl over a 20cm-wide soil area around self-contained pipes, termite damage was prevented for 5 years.

実施例2 化合物A2部、5−4215部をトリオクチルホスフェ
ート25部に溶解し、塩化ビニル原料樹脂50部および
夕〜り18部を加えよく混合した。これを水で20倍に
希釈した樹脂エマルジョンとウレタン系樹脂をツメy先
端で合流させて噴射し家屋下の土壌表層に速硬化性樹脂
膜を形成させたところ、3年間以上白アリの被害を受け
なかった。
Example 2 2 parts of Compound A, 5-4215 parts, were dissolved in 25 parts of trioctyl phosphate, 50 parts of vinyl chloride raw material resin and 18 parts of turmeric were added and mixed well. When this resin emulsion diluted 20 times with water and urethane resin were combined at the tip of the nail and sprayed to form a fast-curing resin film on the soil surface layer under the house, termite damage was prevented for over 3 years. I didn't take it.

〔発明の効果〕〔Effect of the invention〕

本発明の土壌処理試験アリ防除剤は、従来の有機リン系
土壌処理用白アリ防除剤に比べ、人畜に対する安全性、
土壌中の安定性及び白アリ防除効果にすぐれ、極めて有
用な防除薬剤を提供するものである。
The soil treatment test ant control agent of the present invention is safer for humans and livestock than conventional organophosphorus-based termite control agents for soil treatment.
The present invention provides an extremely useful pest control agent with excellent stability in soil and termite control effects.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は試験例2の化合物A、S−421各成分の濃度
と、試験土壌の貫通度との関係を示したものであり、点
線より下部は共力作用領域を示す。 特許出願人 大日本除蟲菊株式会社
FIG. 1 shows the relationship between the concentration of each component of Compound A and S-421 in Test Example 2 and the penetration degree of the test soil, and the area below the dotted line shows the synergistic action area. Patent applicant: Dainippon Jomugiku Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] ジメチル(4−エトキシフェニル){3−(3−フェノ
キシ−4−フルオロフェニル)プロピル}シランとオク
タクロロジプロピルエーテルを含有することを特徴とす
る土壌処理用白アリ防除剤。
A termite control agent for soil treatment characterized by containing dimethyl(4-ethoxyphenyl) {3-(3-phenoxy-4-fluorophenyl)propyl}silane and octachlorodipropyl ether.
JP63128799A 1988-05-26 1988-05-26 Termite control agent for soil treatment Expired - Fee Related JP2610483B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63128799A JP2610483B2 (en) 1988-05-26 1988-05-26 Termite control agent for soil treatment

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63128799A JP2610483B2 (en) 1988-05-26 1988-05-26 Termite control agent for soil treatment

Publications (2)

Publication Number Publication Date
JPH01299203A true JPH01299203A (en) 1989-12-04
JP2610483B2 JP2610483B2 (en) 1997-05-14

Family

ID=14993722

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63128799A Expired - Fee Related JP2610483B2 (en) 1988-05-26 1988-05-26 Termite control agent for soil treatment

Country Status (1)

Country Link
JP (1) JP2610483B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005039287A2 (en) 2003-10-27 2005-05-06 Endura S.P.A. Formulation of a synergistic insecticidal composition as a cyclodextrin-complex
WO2006111570A3 (en) * 2005-04-22 2007-02-01 Endura Spa Biologically active formulation based on cyclodextrin supramolecular complexes
US8025894B2 (en) 2005-04-22 2011-09-27 Endura S.P.A. Innovative formulation
US10149478B2 (en) 2005-04-22 2018-12-11 Endura S.P.A. Biologically active formulation

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005039287A2 (en) 2003-10-27 2005-05-06 Endura S.P.A. Formulation of a synergistic insecticidal composition as a cyclodextrin-complex
WO2005039287A3 (en) * 2003-10-27 2005-06-23 Endura Spa Formulation of a synergistic insecticidal composition as a cyclodextrin-complex
JP2007509853A (en) * 2003-10-27 2007-04-19 エンデュラ ソシエタ ペル アチオニ Synergistic insecticidal composition formulation as a cyclodextrin complex
WO2006111570A3 (en) * 2005-04-22 2007-02-01 Endura Spa Biologically active formulation based on cyclodextrin supramolecular complexes
US8025894B2 (en) 2005-04-22 2011-09-27 Endura S.P.A. Innovative formulation
US10149478B2 (en) 2005-04-22 2018-12-11 Endura S.P.A. Biologically active formulation

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Publication number Publication date
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