JPH0525841B2 - - Google Patents
Info
- Publication number
- JPH0525841B2 JPH0525841B2 JP61314451A JP31445186A JPH0525841B2 JP H0525841 B2 JPH0525841 B2 JP H0525841B2 JP 61314451 A JP61314451 A JP 61314451A JP 31445186 A JP31445186 A JP 31445186A JP H0525841 B2 JPH0525841 B2 JP H0525841B2
- Authority
- JP
- Japan
- Prior art keywords
- boric acid
- cockroaches
- present
- parts
- organic phosphorus
- 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 - Lifetime
Links
- 241001674044 Blattodea Species 0.000 claims description 20
- 239000003795 chemical substances by application Substances 0.000 claims description 19
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 18
- 239000004327 boric acid Substances 0.000 claims description 17
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 11
- 239000011574 phosphorus Substances 0.000 claims description 11
- 229910052698 phosphorus Inorganic materials 0.000 claims description 11
- 239000005871 repellent Substances 0.000 claims description 7
- 230000002940 repellent Effects 0.000 claims description 7
- 229920000858 Cyclodextrin Polymers 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- 239000003094 microcapsule Substances 0.000 claims description 5
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 claims description 5
- 235000010338 boric acid Nutrition 0.000 description 17
- 230000000694 effects Effects 0.000 description 11
- 239000000203 mixture Substances 0.000 description 9
- 230000012447 hatching Effects 0.000 description 7
- ZNOLGFHPUIJIMJ-UHFFFAOYSA-N fenitrothion Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C(C)=C1 ZNOLGFHPUIJIMJ-UHFFFAOYSA-N 0.000 description 6
- 239000002917 insecticide Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000003814 drug Substances 0.000 description 5
- 229940079593 drug Drugs 0.000 description 5
- 239000008187 granular material Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 230000002265 prevention Effects 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 241000238631 Hexapoda Species 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 235000013601 eggs Nutrition 0.000 description 3
- -1 flamethrin Chemical compound 0.000 description 3
- 235000013312 flour Nutrition 0.000 description 3
- SBNFWQZLDJGRLK-RTWAWAEBSA-N (1R)-trans-phenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 SBNFWQZLDJGRLK-RTWAWAEBSA-N 0.000 description 2
- 244000291564 Allium cepa Species 0.000 description 2
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- 244000061456 Solanum tuberosum Species 0.000 description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 239000005667 attractant Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 230000000749 insecticidal effect Effects 0.000 description 2
- 231100000053 low toxicity Toxicity 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 235000013336 milk Nutrition 0.000 description 2
- 239000008267 milk Substances 0.000 description 2
- 210000004080 milk Anatomy 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- 230000000361 pesticidal effect Effects 0.000 description 2
- 229960003536 phenothrin Drugs 0.000 description 2
- 231100000614 poison Toxicity 0.000 description 2
- 235000012015 potatoes Nutrition 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 235000000346 sugar Nutrition 0.000 description 2
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ZCVAOQKBXKSDMS-AQYZNVCMSA-N (+)-trans-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-AQYZNVCMSA-N 0.000 description 1
- FMTFEIJHMMQUJI-NJAFHUGGSA-N 102130-98-3 Natural products CC=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]1[C@@H](C=C(C)C)C1(C)C FMTFEIJHMMQUJI-NJAFHUGGSA-N 0.000 description 1
- 241000238660 Blattidae Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229920002101 Chitin Polymers 0.000 description 1
- 239000001116 FEMA 4028 Substances 0.000 description 1
- 235000019733 Fish meal Nutrition 0.000 description 1
- PWKSKIMOESPYIA-BYPYZUCNSA-N L-N-acetyl-Cysteine Chemical compound CC(=O)N[C@@H](CS)C(O)=O PWKSKIMOESPYIA-BYPYZUCNSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229940024113 allethrin Drugs 0.000 description 1
- 229960004853 betadex Drugs 0.000 description 1
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000005619 boric acid group Chemical class 0.000 description 1
- 235000014121 butter Nutrition 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 230000001079 digestive effect Effects 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- DIRFUJHNVNOBMY-UHFFFAOYSA-N fenobucarb Chemical compound CCC(C)C1=CC=CC=C1OC(=O)NC DIRFUJHNVNOBMY-UHFFFAOYSA-N 0.000 description 1
- 239000004467 fishmeal Substances 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 230000003054 hormonal effect Effects 0.000 description 1
- FYQGBXGJFWXIPP-UHFFFAOYSA-N hydroprene Chemical compound CCOC(=O)C=C(C)C=CCC(C)CCCC(C)C FYQGBXGJFWXIPP-UHFFFAOYSA-N 0.000 description 1
- 229930000073 hydroprene Natural products 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000000366 juvenile effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- VOEYXMAFNDNNED-UHFFFAOYSA-N metolcarb Chemical compound CNC(=O)OC1=CC=CC(C)=C1 VOEYXMAFNDNNED-UHFFFAOYSA-N 0.000 description 1
- RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 description 1
- 229960000490 permethrin Drugs 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229940108410 resmethrin Drugs 0.000 description 1
- VEMKTZHHVJILDY-FIWHBWSRSA-N resmethrin Chemical compound CC1(C)[C@H](C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-FIWHBWSRSA-N 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 229960005199 tetramethrin Drugs 0.000 description 1
- CXBMCYHAMVGWJQ-UHFFFAOYSA-N tetramethrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
本発明は、ホウ酸と有機リン剤のマイクロカプ
セルまたはサイクロデキストリン包接化合物を含
有することを特徴とするゴキブリ駆除剤に関す
る。
ゴキブリ類の駆除方法としては、従来、殺虫剤
の噴霧、塗布する方法、忌避剤を使用する方法、
誘引物質と捕獲器を使用する方法等が知られてい
る。殺虫剤の施用は、積極的な方法であるが、使
用面、残効性の点で必ずしも満足できるものでは
なく、後者の方法は、ゴキブリの発生、増殖に対
しては防止効果がなく、家庭内のゴキブリの一部
のみしか退治することができない。また、最近、
ホウ酸をゴキブリの好む餌、例えば、小麦粉、米
糠、馬鈴薯等の種々の食品に混ぜ、これをゴキブ
リが棲息徘徊する場所に置いて毒餌として使用す
る方法も行なわれているが、ホウ酸の駆除効果は
極めて遅効的で速効性を好む一般消費者には受け
入れられ難い問題がある。
一方、速効性の低毒性有機リン剤もベイト剤の
有効成分として使用されているが、摂餌物質や基
材との混合により有効成分が経時分解を受けやす
く、長期的に効力が持続しない欠点を有してい
る。
本発明者らは、ホウ酸駆除材の欠点である遅効
性を補い、更に有用なゴキブリ駆除剤を採索する
目的で鋭意研究を続けた結果、ホウ酸に、マイク
ロカプセル化あるいはサイクロデキストリンで包
接化された有機リン剤を混合する方法が、本目的
に適合し、速効的でかつ長期間にわたつてすぐれ
た駆除効果を奏することを見い出し本発明を完成
した。
すなわち、有機リン剤単独では、ホウ酸との接
触により分解を受けるのであるが、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によ
り、経時分解は著しく抑えられ、両者の混合が可
能となつた。また、ホウ酸及び有機リン剤とも、
ゴキブリ成虫に対する孵化阻止活性を有していな
いことが一般に知られているが、本発明組成物
は、単に有機リン剤の速効性がホウ酸の効力発現
に加味されるにとどまらず、驚くべきことに、ゴ
キブリ成虫に対して孵化阻止効果も示すことが明
らかとなつた。従つて本発明組成物は、ゴキブリ
の幼虫、成虫のすべてのステージにわたつて駆除
効果を発揮し、総合防除の見地から極めて効率的
かつ実用性の高い駆除剤である。
本発明で使用されるホウ酸としては、螺状滑性
のホウ酸の他、例えば、カルシウム成分を含んだ
ソウカイホウ石(CaNaB5O9・8H2O)、カイホウ
石(Ca2B6O11・5H2O)、プライス石
(Ca5B12O23・9H2O)、ハイドロボラサイト
(MgCaB6O11・6H2O)などの微粉状天然原料な
ど種々のホウ酸化合物も含まれる。ホウ酸のゴキ
ブリに対する殺虫作用機構については未だ不明な
部分が多いが、一説には、ホウ酸の摂食により渇
水状態を惹起せしめ消化機能を停止させるものと
考えられている。
一方、有機リン剤は、単独又は2種以上の混合
物が用いられ、特にその種類は限定されるもので
はないが、好適なものとして低毒性のフエニトロ
チオン、デイプテレツクス、ダイアジノンなどを
あげることができる。また、有機リン剤のマイク
ロカプセル化あるいは、サイクロデキストリン包
接化においては、何ら特別の技術は必要とせず、
従来の公知技術、プロセスにより、粉状、ペース
ト状、乳化状あるいは液状に種々フオーミユレー
シヨンが可能である。
本発明のゴキブリ駆除剤には、上記ホウ酸が5
〜80重量%、または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された有機リン剤が
1〜70重量%配合され、更に必要に応じて、ゴキ
ブリの食嗜好性が高くなるように、小麦粉、馬鈴
薯、玉ねぎ、バター、魚粉、砂糖などの食品や、
あるいは誘引剤、賦形剤、水などが適宜添加され
て、錠剤、顆粒、粉状、ペースト状など任意の剤
型に成型される。また、本発明の組成物に、他の
殺虫剤、例えば、アレスリン、フタールスリン、
フラメトリン、フエノトリン、ペルメトリン、レ
スメトリンなどのピレスロイド剤や、NAC、
MTMC、BPMCなどのカーバメート剤や、ハイ
ドロプレンのような幼若ホルモン様化合物、キチ
ン合成阻害剤、あるいは、共力剤や、香料などを
適宜混合することによつて効果のすぐれた多目的
組成物が得られ、労力の省力化も充分期待しえる
ものである。
こうして得られた本発明駆除剤は使用が簡便で
あり、これを家庭内のゴキブリの出る場所に配置
すれば、毒餌剤として長期間効力を持続し、摂食
したゴキブリは、幼虫、成虫を問わず、有機リン
剤の速効性と、ホウ酸の遅効性により確実に死に
至るものである。しかも摂食した雌成虫には、孵
化阻止効果も及ぼすためその成虫から産卵された
卵の孵化率は極端に低く、従つてゴキブリの生息
密度を抑えるうえで多大なメリツトがある。ま
た、本発明ゴキブリ駆除剤は、ゴキブリに対して
作用機作の全く異なる2種の成分を混合している
ため、殺虫剤に対する抵抗性の発達を抑える面か
らも効果的である。
次に本発明の実施例について具体的に説明する
が、本発明がこれらに限定されるものでないこと
はもちろんである。
実施例 1
工業用ホウ酸60部、フエニトロチオンマイクロ
カプセル20部(フエニトロチオンとして8部)、
小麦粉10部、砂糖5部、牛乳5部を混練してだん
ご状の固まりを作り、これを熱風乾燥機に入れて
80℃にて2時間乾燥させ、だんご状の製剤を得
た。
実施例 2
工業用ホウ酸40部、ダイアジノン−βサイクロ
デキストリン包接化合物40部(ダイアジノンとし
て5部)、粉砕した玉ねぎ8部、フエノトリン1
部、でん粉6部、色粉少量、水5部を加えてよく
混合し、タブレツト機で打錠して錠剤を得た。
実施例 3
カイホウ石を100μm以下に微粉砕し、その微
粉末50部、デイプテレツクスマイクロカプセル25
部(デイプテレツクスとして10部)、米糠15部、
牛乳10部を加えてよく混練し、顆粒機をとおして
顆粒状製剤を得た。
試験例 1
約30cm立方のプラスチツク製容器の中に、製造
後1定期間経過する毎に、実施例1で得られただ
んご(径約1cmの球形)2ケを入れ、更にチヤバ
ネゴキブリ♂♀成虫10頭を放飼して経過日数と累
計死虫数を観察した。コントロールとして、薬剤
がホウ酸のみのもの(No.2)、フエニトロチオン
のみのもの(No.3)、フエニトロチオンマイクロ
カプセルのみのもの(No.4)、及び無薬剤のもの
(No.5)を用いた。
なお、MSはカイクロカプセル、CDはサイク
ロデキストリン包接化合物を表わす。
The present invention relates to a cockroach repellent characterized by containing microcapsules of boric acid and an organic phosphorus agent or a cyclodextrin clathrate compound. Conventional methods for exterminating cockroaches include spraying and applying insecticides, using repellents,
Methods using attractants and traps are known. Although the application of insecticides is a proactive method, it is not always satisfactory in terms of usage and residual effectiveness.The latter method is not effective in preventing the emergence and proliferation of cockroaches, and Only some of the cockroaches inside can be exterminated. Also, recently,
Another method is to mix boric acid with various foods that cockroaches like, such as flour, rice bran, and potatoes, and place it in areas where cockroaches roam and use it as poison bait. The effect is extremely slow, making it difficult for general consumers who prefer quick-acting effects to accept it. On the other hand, fast-acting, low-toxicity organophosphorus agents are also used as active ingredients in bait agents, but the active ingredients tend to decompose over time when mixed with feeding substances and substrates, and their effectiveness does not last long. have. The inventors of the present invention have conducted intensive research to find a more useful cockroach repellent that can compensate for the slow-acting drawback of boric acid repellents. The present invention has been completed by discovering that a method of mixing an organic phosphorus agent is suitable for the present purpose, is fast-acting, and exhibits an excellent extermination effect over a long period of time. That is, when an organic phosphorus agent is used alone, it is decomposed by contact with boric acid, but by microencapsulation or cyclodextrin inclusion, decomposition over time is significantly suppressed, and mixing of the two becomes possible. Also, boric acid and organic phosphorus agents
Although it is generally known that the composition of the present invention does not have hatching prevention activity against adult cockroaches, it is surprising that the composition of the present invention not only combines the quick-acting properties of an organic phosphorus agent with the effectiveness of boric acid. In addition, it was revealed that it also has an effect on preventing adult cockroaches from hatching. Therefore, the composition of the present invention exhibits exterminating effects on all stages of cockroach larvae and adults, and is an extremely efficient and highly practical exterminating agent from the standpoint of comprehensive control. Examples of the boric acid used in the present invention include, in addition to spirally slippery boric acid, for example, kaioborite (CaNaB 5 O 9 8H 2 O) containing calcium components, kaioborite (Ca 2 B 6 O 11・5H 2 O), priceite (Ca 5 B 12 O 23・9H 2 O), hydroborasite (MgCaB 6 O 11・6H 2 O) and other finely powdered natural raw materials and various boric acid compounds are also included. Although much remains unclear about the insecticidal mechanism of boric acid against cockroaches, one theory is that ingestion of boric acid induces a state of drought and stops the digestive function. On the other hand, the organic phosphorus agent may be used alone or as a mixture of two or more, and the type thereof is not particularly limited, but preferred examples include fenitrothion, dipterex, diazinon, etc., which have low toxicity. In addition, no special technology is required for microencapsulation of organic phosphorus agents or cyclodextrin inclusion.
Various formulations such as powder, paste, emulsion or liquid can be made using conventional techniques and processes. The cockroach repellent of the present invention contains 5 boric acids.
~80% by weight, or 1~70% by weight of microencapsulated or cyclodextrin-encapsulated organic phosphorus agents, and if necessary, flour, potatoes, Foods such as onions, butter, fish meal, sugar,
Alternatively, attractants, excipients, water, etc. are added as appropriate, and the mixture is molded into any desired dosage form such as tablets, granules, powder, and paste. The composition of the present invention may also contain other insecticides, such as allethrin, phthalthrin,
Pyrethroids such as flamethrin, phenothrin, permethrin, and resmethrin, NAC,
By appropriately mixing carbamates such as MTMC and BPMC, juvenile hormone-like compounds such as hydroprene, chitin synthesis inhibitors, synergists, and fragrances, highly effective multipurpose compositions can be created. This can be expected to save labor. The pesticidal agent of the present invention obtained in this way is easy to use, and if it is placed in a place where cockroaches are found in the home, it will remain effective as a poisonous bait for a long time, and the cockroaches that eat it will be able to control both larvae and adults. First, the fast-acting nature of organic phosphorus agents and the slow-acting nature of boric acid will definitely lead to death. Moreover, since it also exerts a hatching prevention effect on the female adult that feeds on it, the hatching rate of the eggs laid by the adult is extremely low, so it has a great advantage in suppressing the population density of cockroaches. Moreover, since the cockroach repellent of the present invention contains two types of components having completely different mechanisms of action against cockroaches, it is also effective in suppressing the development of resistance to insecticides. Next, examples of the present invention will be specifically described, but it goes without saying that the present invention is not limited to these examples. Example 1 60 parts of industrial boric acid, 20 parts of fenitrothion microcapsules (8 parts as fenitrothion),
Knead 10 parts of flour, 5 parts of sugar, and 5 parts of milk to make a dumpling-like mass, then put it in a hot air dryer.
It was dried at 80°C for 2 hours to obtain a dumpling-shaped preparation. Example 2 40 parts of industrial boric acid, 40 parts of diazinon-β cyclodextrin clathrate compound (5 parts as diazinon), 8 parts of crushed onion, 1 part of phenothrin
1 part, 6 parts of starch, a small amount of colored powder, and 5 parts of water were added, mixed well, and compressed using a tablet machine to obtain tablets. Example 3: Finely pulverized kaiborosite to 100 μm or less, 50 parts of the fine powder, 25 diptelex microcapsules
division (10 divisions as dipterex), 15 divisions of rice bran,
10 parts of milk was added, kneaded well, and passed through a granulator to obtain a granular preparation. Test Example 1 In a plastic container approximately 30 cm cubic in size, two dangos (spherical with a diameter of approximately 1 cm) obtained in Example 1 were placed every 1 period after production, and a Chinese cockroach♂♀ was placed in the container. Ten adult insects were released and the number of days elapsed and the total number of dead insects were observed. As controls, the drug was only boric acid (No. 2), the drug was only fenitrothion (No. 3), the drug was only fenitrothion microcapsules (No. 4), and the drug was not used (No. 5). was used. Note that MS stands for cyclocapsule and CD stands for cyclodextrin inclusion compound.
【表】
試験の結果、本発明の駆除剤は、5ケ月、10ケ
月後のように長時間後においても速効的でかつ高
い殺虫効力を示し、そのレベルは、ホウ酸単剤
(No.2)と、フエニトロチオンMC単剤(No.4)
のそれぞれの効力から予想される以上の相乗的な
ものであつた。
試験例 2
本発明駆除剤のゴキブリ成虫に対する孵化阻止
効果をみるために、実施例3で得られた顆粒を、
薬剤無添加の顆粒4倍量と混合して薬剤濃度を1/
5に希釈したものを供試した。
約30cm立方のプラスチツク容器の中に、上記顆
粒を1gずつ入れ、ワモンゴキブリ♂♀成虫各5
匹ずつを放飼した。5日後、該成虫を容器から除
き、その間産卵された卵の孵化率を求めたところ
次の如くであつた。[Table] As a result of the test, the insecticidal agent of the present invention showed fast-acting and high insecticidal efficacy even after a long period of time, such as after 5 or 10 months, and its level was higher than that of boric acid single agent (No. 2). ) and fenitrothion MC single agent (No. 4)
The effect was more synergistic than expected based on their respective efficacy. Test Example 2 In order to examine the hatching prevention effect of the insecticide of the present invention on adult cockroaches, the granules obtained in Example 3 were
Mix with 4 times the amount of drug-free granules to reduce the drug concentration to 1/1.
A sample diluted to 5 was used. Place 1 g each of the above granules in a plastic container of approximately 30 cm cube, and add 5 adult male and female American cockroaches each.
The animals were released one by one. After 5 days, the adult insects were removed from the container, and the hatching rate of the eggs laid during that time was determined as follows.
【表】
供試番号No.1及びNo.3の産卵数が少ないのはデ
イプテレツクスの速効性が寄与したものと思われ
る。本発明駆除剤(No.1)は、ホウ酸単剤(No.
2)、有機リン剤単剤(No.3)にはみられない顕
著な孵化阻止効果を示し、混合による新しい効果
の付与が認められた。[Table] The low number of eggs laid in test numbers No. 1 and No. 3 is thought to be due to the fast-acting properties of Diptelecus. The pesticidal agent of the present invention (No. 1) is a boric acid single agent (No.
2) showed a remarkable hatching prevention effect that was not seen with the organic phosphorus agent alone (No. 3), and it was observed that a new effect was imparted by mixing.
Claims (1)
たはサイクロデキストリン包接化合物を含有する
ことを特徴とするゴキブリ駆除剤。1. A cockroach repellent characterized by containing boric acid and microcapsules of an organic phosphorus agent or a cyclodextrin clathrate compound.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP31445186A JPS63166812A (en) | 1986-12-27 | 1986-12-27 | Cockroach expellent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP31445186A JPS63166812A (en) | 1986-12-27 | 1986-12-27 | Cockroach expellent |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63166812A JPS63166812A (en) | 1988-07-11 |
JPH0525841B2 true JPH0525841B2 (en) | 1993-04-14 |
Family
ID=18053514
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP31445186A Granted JPS63166812A (en) | 1986-12-27 | 1986-12-27 | Cockroach expellent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63166812A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ZA903739B (en) * | 1989-05-27 | 1991-03-27 | Sumitomo Chemical Co | A poison bait for control of noxious insects |
JPH0679532B2 (en) * | 1991-06-07 | 1994-10-12 | 敏行 高坂 | Cockroach attraction poison bait and cockroach attraction insecticide |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57142906A (en) * | 1981-02-26 | 1982-09-03 | Sumitomo Chem Co Ltd | Insecticide |
JPS58144304A (en) * | 1982-02-19 | 1983-08-27 | Sumitomo Chem Co Ltd | Organophosphorus-based insecticide composition |
-
1986
- 1986-12-27 JP JP31445186A patent/JPS63166812A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57142906A (en) * | 1981-02-26 | 1982-09-03 | Sumitomo Chem Co Ltd | Insecticide |
JPS58144304A (en) * | 1982-02-19 | 1983-08-27 | Sumitomo Chem Co Ltd | Organophosphorus-based insecticide composition |
Also Published As
Publication number | Publication date |
---|---|
JPS63166812A (en) | 1988-07-11 |
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