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JPS6049161B2 - Composition for killing ants - Google Patents
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JPS6049161B2 - Composition for killing ants - Google Patents

Composition for killing ants

Info

Publication number
JPS6049161B2
JPS6049161B2 JP52112171A JP11217177A JPS6049161B2 JP S6049161 B2 JPS6049161 B2 JP S6049161B2 JP 52112171 A JP52112171 A JP 52112171A JP 11217177 A JP11217177 A JP 11217177A JP S6049161 B2 JPS6049161 B2 JP S6049161B2
Authority
JP
Japan
Prior art keywords
composition
tae
present
trans
hereinafter referred
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.)
Expired
Application number
JP52112171A
Other languages
Japanese (ja)
Other versions
JPS5446835A (en
Inventor
啓暢 高橋
邦彦 富樫
泰 村上
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.)
Chugai Pharmaceutical Co Ltd
Original Assignee
Chugai Pharmaceutical 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 Chugai Pharmaceutical Co Ltd filed Critical Chugai Pharmaceutical Co Ltd
Priority to JP52112171A priority Critical patent/JPS6049161B2/en
Publication of JPS5446835A publication Critical patent/JPS5446835A/en
Publication of JPS6049161B2 publication Critical patent/JPS6049161B2/en
Expired legal-status Critical Current

Links

Landscapes

  • Chemical And Physical Treatments For Wood And The Like (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

【発明の詳細な説明】 本発明は、イソシアヌール酸トリアリルエステル(以下
「TAE」と略称する)とピレスロイド系殺虫剤を有効
成分として含有する段目アリ用組成物に関するものてあ
る。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a composition for stage ants containing triallyl isocyanuric acid ester (hereinafter abbreviated as "TAE") and a pyrethroid insecticide as active ingredients.

本発明者等は、TAEが木材腐朽菌に対して活性を示す
とともに、木材およびセルローズ性材料に多大の被害を
与える白アリに対し強い活性を示すことを見出した。
The present inventors have discovered that TAE exhibits activity against wood-decaying fungi and also exhibits strong activity against termites, which cause great damage to wood and cellulosic materials.

このTAEが白アリに対して活性を示す特色としては、
比較的高薬量て強い段目アリ活性を示し、低薬量に於い
ては白アリの食害を防止する作用を示し段目アリ活性を
発現する。
The characteristics of this TAE showing activity against termites include:
At relatively high dosages, it exhibits strong tier ant activity, and at low dosages, it exhibits the effect of preventing termite feeding damage and exhibits tier ant activity.

しかも、TAEは白アリに対する活性が長時間にわたり
残効力を示す。一方、本発明で用いられる段目アリ作用
を有するピレスロイド系殺虫剤としては、例えば(+)
−3−アリルー1−メチルー4−オキソー2−シクロペ
ンテニールー (十)一トランスークリサンテメート
(以下一般名「エスパーオール」という)、3−フエノ
キシベンジルーシス/トランスー 3−(2、2−ジク
ロロビニール)−2、2−ジメチルプロパンー1−カル
ボキシラート (以下一般名「パーメスリン」という)
、(±)−3−アリルー2−メチルー4−オキソー2−
シクロペンテールー(±)−シス/トランスークリサン
テメート (以下一般名「アレスリン」という)、5ー
ベンジルー3−フリルメチルー(±)−シス/トランス
ークリサンテメート (以下一般名丁レスメトリン」と
いう)、5−ベンジルー3−フリルメチルー(+)−シ
ス/トランスークリサンテメート(以下一般名「d−レ
スメトリン」という)、N−(3、4、5、6−テトラ
ヒドロフタルイミド)メチル−(±)−シス/トランス
ークリサン1テメート (以下一般名「フタルスリン」
という)および3−フェノキシベンジル−(+)−シス
/トランスークリサンテメート (以下一般名「dーフ
エノトリン」という)が挙げられる。
Moreover, TAE exhibits residual activity against termites over a long period of time. On the other hand, as the pyrethroid insecticide having a step ant action used in the present invention, for example, (+)
-3-aryl-1-methyl-4-oxo-2-cyclopentenyl-(10)-trans-chrysanthemate
(hereinafter referred to as "Esperol"), 3-phenoxybenzylosis/trans-3-(2,2-dichlorovinyl)-2,2-dimethylpropane-1-carboxylate (hereinafter referred to as "Permethrin") )
, (±)-3-aryl-2-methyl-4-oxo2-
Cyclopentele-(±)-cis/trans-chrysanthemate (hereinafter referred to as "allethrin"), 5-benzy-3-furylmethyl-(±)-cis/trans-chrysanthemate (hereinafter referred to as "common name resmethrin") , 5-benzyl-3-furylmethyl-(+)-cis/trans-chrysanthemate (hereinafter referred to as "d-resmethrin"), N-(3,4,5,6-tetrahydrophthalimido)methyl-(±)- Cis/transucrysan 1 temate (hereinafter generic name "phthalthrin")
) and 3-phenoxybenzyl-(+)-cis/trans-chrysanthemate (hereinafter referred to by the common name "d-phenotrin").

このピレスロイド系殺虫剤の白アリに対する活フ性の特
色としては、低薬量に於て・も速効性を示し、その上低
毒性である。
The pyrethroid insecticide's activity against termites is characterized by its rapid effectiveness even at low dosages and low toxicity.

本発明は上記したように、TAEとピレスロイド系殺虫
剤の特色を利用し、これら2種の薬剤を混合することに
より少量て残効性と速効性を兼ね備えた極めて有用な殺
白アリ用組成物である。
As described above, the present invention utilizes the characteristics of TAE and pyrethroid insecticides, and by mixing these two types of agents, an extremely useful termite-killing composition that has both residual effect and immediate effect in a small amount is produced. It is.

しかも、本発明の組成物の特徴はTAEとピレスロイド
系殺虫剤の各々の活性が相加つただけでなく、白アリに
対する作用部位、作用機構が相異なつて相乗的に作用し
ているからである。本発明の組成物におけるL正とピレ
スロイド系殺虫剤の混合に際しては、TAEは常温て液
体てあり、ピレスロイド系殺虫剤とも各種溶剤に溶け易
いから各成分を使用目的、使用場面等に応じて広い範囲
て適宜に混合し得る。
Furthermore, the composition of the present invention is characterized by not only the additive activities of TAE and pyrethroid insecticides, but also the fact that their action sites and mechanisms of action against termites are different and act synergistically. . When mixing L-positive and pyrethroid insecticides in the composition of the present invention, since TAE is liquid at room temperature and both pyrethroid insecticides and pyrethroid insecticides are easily soluble in various solvents, each component can be mixed in a wide variety of ways depending on the purpose of use and usage situation. They can be mixed as appropriate within a range.

本発明の組成物の効果を最も有効に発揮するためには、
TAEに対してピレスロイド系殺虫剤の混合割合は2〜
40%(重量%)が最も好ましい。本発明の実施に際し
ては、本発明の組成物の1成分てあるTAEが安定な化
合物であり、常温では液体てあるため組成物をそのまま
ても使用することが可能てある。
In order to most effectively exhibit the effects of the composition of the present invention,
The mixing ratio of pyrethroid insecticide to TAE is 2~
40% (wt%) is most preferred. When carrying out the present invention, since TAE, which is one of the components of the composition of the present invention, is a stable compound and is liquid at room temperature, it is possible to use the composition as it is.

しかし、本発明の目的を最も効果的に発揮するために油
剤または乳剤として使用することが好ましい。また、使
用目的あるいは使用場面に応じて水和剤,懸濁剤,粉剤
,粒剤,・エアゾール,燻煙剤、燻蒸剤としても使用出
来る。製剤化に当つては、担体として固体、液体または
気体のいずれでもよく、またこれらの組合わせでもよい
However, in order to most effectively achieve the purpose of the present invention, it is preferable to use it as an oil or emulsion. It can also be used as a wettable powder, suspension agent, powder, granule, aerosol, fumigant, or fumigant depending on the purpose or situation. In formulation, the carrier may be solid, liquid or gas, or a combination thereof.

ここでいう担体としては、例えばタル2ク,クレー,カ
オリン,珪こう土,ホワイトカーボン,炭酸カルシウム
,塩素酸カリウム,硝石,木粉,ニトロセルローズ,澱
粉,アラビアゴム末,水,アルコール,ケロシン,ナフ
サ,キシレン,メチルナフタリン,ベンゼン,アセトン
,空3気,窒素,炭酸ガス,フレオン,塩化ビニール,
プロパン,ブタン等が用いられる。また、本発明組成物
に補助剤、例えは展着剤,乳化剤,分散剤,湿展剤等を
添加してもよい。
Examples of the carrier here include talc, clay, kaolin, diatomaceous earth, white carbon, calcium carbonate, potassium chlorate, saltpeter, wood flour, nitrocellulose, starch, gum arabic powder, water, alcohol, kerosene, Naphtha, xylene, methylnaphthalene, benzene, acetone, air, nitrogen, carbon dioxide, freon, vinyl chloride,
Propane, butane, etc. are used. Further, auxiliary agents such as spreading agents, emulsifiers, dispersants, wetting agents, etc. may be added to the composition of the present invention.

また、使用目的に応じて、本発明組成物を他の殺虫3.
剤,殺菌剤,防腐剤と併用することもてきる。実際の使
用に際しては、本発明組成物の含有量は使用場面、使用
目的あるいは製剤の形態により広い濃度範囲にわたつて
変化させうることは当然であるが、一般に好ましい使用
濃度は0.1〜10%4Cの範囲が適当である。また、
組成物の処理方法としては、木質材に吸入,散布,塗布
,浸漬処理するか、あるいは土壌処理等の適宜の方法て
使用し得る。次に実験例を挙げて説明する。
Depending on the purpose of use, the composition of the present invention may also be used to kill other insects.
It can also be used in combination with disinfectants, fungicides, and preservatives. In actual use, it goes without saying that the content of the composition of the present invention can be varied over a wide range of concentrations depending on the use situation, purpose of use, or form of preparation; however, the generally preferred concentration is 0.1 to 10. A range of %4C is suitable. Also,
The composition can be treated by any appropriate method such as inhalation, spraying, coating, or immersion treatment on wood materials, or soil treatment. Next, an explanation will be given using an experimental example.

実験例 イエシロアリに対する効力試験 径9C!RLの円形沖紙に各薬剤の所定濃度の有効成分
を含むアセトン溶液1m1を処理して風乾し、この■紙
を径9cmのペトリ皿の底面に敷き1m1の水を含ませ
た。
Experimental example Efficacy test against house termites Diameter 9C! RL circular paper was treated with 1 ml of an acetone solution containing the active ingredients of each drug at a predetermined concentration and air-dried, and this paper was placed on the bottom of a Petri dish with a diameter of 9 cm and impregnated with 1 ml of water.

次いで、松材より取出したイエシロアリの職蟻20頭を
入れてガラスの蓋をし、25±2℃の恒温条件下におき
、その後の経過を観察した。その結果を次表に示す。次
に実施例を挙げて説明する。
Next, 20 worker ants of the domestic termite taken out from the pine wood were placed in the container, covered with a glass lid, and kept at a constant temperature of 25±2° C., and the subsequent progress was observed. The results are shown in the table below. Next, an example will be given and explained.

起施例1 TAE4重量部 エスバイオール 0.4〃 カワカゾール(川崎化成社製)95.6〃これらをよく
混合して油剤として用いる。
Example 1 TAE 4 parts by weight Esvirol 0.4 Kawakazol (manufactured by Kawasaki Kasei Co., Ltd.) 95.6 These were mixed well and used as an oil agent.

辷施例2 TAE40重量部 パーメスリン 10〃 ドデシルベンジルスルフホン酸カ ルシウム塩 5 〃 ポリオキシエチレンアルキルアリ ルエーテル 5 〃 キシレン 40〃これらをよく
混合して乳剤として用いる。
Example 2 TAE 40 parts by weight Permethrin 10 Dodecylbenzyl sulfonic acid calcium salt 5 Polyoxyethylene alkyl allyl ether 5 Xylene 40 These were thoroughly mixed and used as an emulsion.

実施例3 TAE4重量部 アレスリン 0.5〃 ホワイトカーボン 3 〃 クレー 92.5〃これらをよ
く混合し、粉砕して粉剤として用いる。
Example 3 TAE 4 parts by weight Allethrin 0.5 White carbon 3 Clay 92.5 These were mixed well and ground to use as a powder.

Claims (1)

【特許請求の範囲】[Claims] 1 イソシアヌール酸トリアリルエステルとピレスロイ
ド系殺虫剤を有効成分として含有することを特徴とする
殺白アリ用組成物。
1. A termite-killing composition characterized by containing isocyanuric acid triallyl ester and a pyrethroid insecticide as active ingredients.
JP52112171A 1977-09-20 1977-09-20 Composition for killing ants Expired JPS6049161B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP52112171A JPS6049161B2 (en) 1977-09-20 1977-09-20 Composition for killing ants

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP52112171A JPS6049161B2 (en) 1977-09-20 1977-09-20 Composition for killing ants

Publications (2)

Publication Number Publication Date
JPS5446835A JPS5446835A (en) 1979-04-13
JPS6049161B2 true JPS6049161B2 (en) 1985-10-31

Family

ID=14580015

Family Applications (1)

Application Number Title Priority Date Filing Date
JP52112171A Expired JPS6049161B2 (en) 1977-09-20 1977-09-20 Composition for killing ants

Country Status (1)

Country Link
JP (1) JPS6049161B2 (en)

Also Published As

Publication number Publication date
JPS5446835A (en) 1979-04-13

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