JPH01143806A - Poisonous bait agent for exterminating insect pest - Google Patents
Poisonous bait agent for exterminating insect pestInfo
- Publication number
- JPH01143806A JPH01143806A JP62304142A JP30414287A JPH01143806A JP H01143806 A JPH01143806 A JP H01143806A JP 62304142 A JP62304142 A JP 62304142A JP 30414287 A JP30414287 A JP 30414287A JP H01143806 A JPH01143806 A JP H01143806A
- Authority
- JP
- Japan
- Prior art keywords
- insect
- agent
- active ingredient
- bait agent
- compounds
- 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
Links
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- 235000019259 sodium dehydroacetate Nutrition 0.000 description 1
- 229940079839 sodium dehydroacetate Drugs 0.000 description 1
- 235000010352 sodium erythorbate Nutrition 0.000 description 1
- 239000004320 sodium erythorbate Substances 0.000 description 1
- JXKPEJDQGNYQSM-UHFFFAOYSA-M sodium propionate Chemical compound [Na+].CCC([O-])=O JXKPEJDQGNYQSM-UHFFFAOYSA-M 0.000 description 1
- 235000010334 sodium propionate Nutrition 0.000 description 1
- 239000004324 sodium propionate Substances 0.000 description 1
- 229960003212 sodium propionate Drugs 0.000 description 1
- DSOWAKKSGYUMTF-GZOLSCHFSA-M sodium;(1e)-1-(6-methyl-2,4-dioxopyran-3-ylidene)ethanolate Chemical compound [Na+].C\C([O-])=C1/C(=O)OC(C)=CC1=O DSOWAKKSGYUMTF-GZOLSCHFSA-M 0.000 description 1
- RBWSWDPRDBEWCR-RKJRWTFHSA-N sodium;(2r)-2-[(2r)-3,4-dihydroxy-5-oxo-2h-furan-2-yl]-2-hydroxyethanolate Chemical compound [Na+].[O-]C[C@@H](O)[C@H]1OC(=O)C(O)=C1O RBWSWDPRDBEWCR-RKJRWTFHSA-N 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 229960000984 tocofersolan Drugs 0.000 description 1
- 239000010497 wheat germ oil Substances 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
- OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【発明の詳細な説明】 〔産業上の利用分野〕 この発明は害虫駆除用毒餌剤に関するものである。[Detailed description of the invention] [Industrial application field] This invention relates to a poisonous bait for pest control.
従来、害虫駆除用毒餌剤(ベイト剤)としては粉末状の
ものが上布されている。しかし、粉末状の毒餌剤は使用
する際に手に付着したり、所定の場所に配置した後も飛
散して周辺を汚染したり、また、幼児やペットが誤食す
るなど、一般消費者が取扱う上で、特に安全面で、数多
くの問題がある。したがって、このような問題を解決す
るために、たとえばホウ酸を主剤とした錠剤型の毒餌剤
が既に市販されているが、害虫特にゴキブリに対しては
その効力の面から有効成分としてのホウ酸の含有量は2
0〜30%程度とかなり多い、そのため人畜特に幼児に
対しては決して安全であるとは言えない、たとえば第1
1日局解説書C−1475にはホウ酸5%含有のてんか
粉を使用した幼児の死亡例も見受けられる程であり、ホ
ウ酸の誤用による事故の危険性に対しては充分配慮する
必要が認められている。また、ゴキブリに対するホウ酸
の効力発現の過程においていわゆる下痢症状を呈して死
に至るので、ゴキブリの生息場所(食器棚や流し台)等
の周辺に軟排泄物が多(付着し、非常に不衛生であり、
白壁、クロス材等の建材を汚し、美観が損われるという
事態も起こる。BACKGROUND ART Conventionally, poisonous baits for exterminating pests have been applied in powder form. However, powdered poison baits can get on your hands when you use them, scatter and contaminate the surrounding area even after they are placed in a designated place, or be accidentally ingested by young children or pets. There are many problems in handling it, especially in terms of safety. Therefore, to solve this problem, for example, tablet-shaped poison baits containing boric acid as the main ingredient are already on the market, but boric acid as an active ingredient is not effective against pests, especially cockroaches. The content of is 2
The percentage is quite high, about 0 to 30%, so it cannot be said to be safe for humans, animals, and especially young children.
According to the 1st Bureau Manual C-1475, there are even cases of infant deaths caused by using bean powder containing 5% boric acid, and it is necessary to give sufficient consideration to the risk of accidents due to misuse of boric acid. It recognized. In addition, in the process of exerting the effect of boric acid on cockroaches, they exhibit so-called diarrhea symptoms and die, so there is a lot of soft excrement (adhering to them) around cockroach habitats (cupboards, sinks), etc., making it extremely unsanitary. can be,
Situations also occur in which building materials such as white walls and cloth are stained and the aesthetic appearance is impaired.
一方、人畜毒性の低い害虫駆除剤、たとえば昆虫幼若ホ
ルモン様殺虫剤または昆虫キチン形成阻害剤を有効成分
とした錠剤型のゴキブリ駆除用毒餌剤の場合には、これ
らの有効成分の効力はホウ酸に比べてきわめて大きいこ
とから、製剤中に配合する有効成分の量は、ホウ酸製剤
に比較して少量でよく、製剤の安全性は好ましい方向に
改善されると言えるが、一般に有機リン化合物、ピレス
ロイド化合物、カーバメイト化合物等の有効成分を用い
て錠剤化すると、それぞれの有効成分特有の臭いによっ
て、ゴキブリが錠剤を忌避し、その結果、誘引喫食効果
が悪くなり、殺虫効果が著しく低下することが知られて
おり、上記の昆虫幼若ホルモン様化合物または昆虫キチ
ン形式阻害化合物についても例外ではない、さらには、
これらの殺虫剤を有効成分とした製剤では、それら有効
成分が系内の微量水分で加水分解を受け、その分解によ
って有効成分自体の含有率が低下し、効力がきわめて悪
くなる場合がある。On the other hand, in the case of tablet-shaped poison baits for exterminating cockroaches that contain insecticides with low toxicity to humans and animals, such as insecticides similar to insect juvenile hormones or insect chitin formation inhibitors, the efficacy of these active ingredients is limited. Since it is extremely large compared to boric acid, the amount of active ingredient added to the formulation can be small compared to boric acid formulations, and it can be said that the safety of the formulation is improved in a favorable direction. When tablets are made with active ingredients such as pyrethroid compounds, carbamate compounds, etc., cockroaches avoid the tablets due to the unique odor of each active ingredient, resulting in poor attraction and eating effects and a significant drop in insecticidal efficacy. is known, and the above-mentioned insect juvenile hormone-like compounds or insect chitin-form inhibiting compounds are no exception.
In preparations containing these insecticides as active ingredients, the active ingredients are hydrolyzed by trace amounts of moisture in the system, and this decomposition reduces the content of the active ingredients themselves, resulting in extremely poor efficacy.
このように昆虫幼若ホルモン様殺虫剤、または昆虫キチ
ン形成阻害剤をゴキブリ等の害虫駆除剤として毒餌化す
る場合、有効成分の安定性および害虫の誘引喫食効果、
殺虫効果などの点で充分とは言えないという問題点があ
った。In this way, when using an insect juvenile hormone-like insecticide or an insect chitin formation inhibitor as poison bait as a pest control agent for cockroaches and other pests, the stability of the active ingredient and the insect attraction and feeding effect,
There was a problem that the insecticidal effect was not sufficient.
上記の問題点を解決するために、この発明は昆虫幼若ホ
ルモン様化合物および昆虫キチン形成阻害化合物からな
る群の中から選ばれる1種以上の昆虫成長制御剤、結晶
セルロース、穀類粉、さらに毒餌剤全量に対し、0.1
〜10.0重量%の植物精油およびIO1θ〜40.0
重量%の糖を主要成分とし、これを打錠した害虫駆除用
毒餌剤とする手段を採用したものである。以下その詳細
を述べる。In order to solve the above problems, the present invention provides one or more insect growth regulators selected from the group consisting of insect juvenile hormone-like compounds and insect chitin formation inhibiting compounds, crystalline cellulose, cereal flour, and poison bait. 0.1 based on the total amount of agent
~10.0% by weight of plant essential oil and IO1θ~40.0
The main ingredient is sugar at % by weight, and this is compressed into a poisonous bait for exterminating pests. The details will be described below.
まず、この発明において、昆虫幼若ホルモン様化合物と
しては、第1表で示されるような、ドデカジェノエート
系化合物、オキシムエーテル系化合物、ピリジルエーテ
ル化合物、カーバメート系化合物などが挙げられる。さ
らに、昆虫キチン形成阻害化合物としては第2表で示さ
れるようなベンゾイルフェニルウレア系化合物などが挙
げられる。First, in the present invention, insect juvenile hormone-like compounds include dodecagenoate compounds, oxime ether compounds, pyridyl ether compounds, carbamate compounds, etc. as shown in Table 1. Furthermore, examples of insect chitin formation inhibiting compounds include benzoyl phenyl urea compounds as shown in Table 2.
つぎに、このような殺虫性化合物からなる群の第1表
第2表
中から選ばれる1種以上の殺虫性化合物の使用量は、化
合物の種類および対象害虫の種類にもよるが、通常、毒
餌剤全量に対し、0.01〜2.0重量%である。そし
て、結晶セルロースとしては、たとえば旭化成工業■製
アビセルを代表的な例として挙げることが出来、その使
用量は通常、毒餌剤全量に対し、20.0〜60.0重
量%である。また穀類粉末としては、たとえばジャガイ
モ、サツマイモ、トウモロコシなどのデンプン粉、小麦
粉、米粉、トウモロコシ粉などの穀物粉を例示すること
が出来、その使用量は通常、毒餌剤全量に対し10.0
〜80.0重量%である。さらに植物精油としては大豆
油、菜種油、ゴマ油、小麦胚芽油などを好ましいものの
例として挙げることが出来、糖としては、シ=II!、
ブドウ糖、果糖、乳糖、黒砂糖、赤砂糖、三温糖などを
列挙することが出来るが、中でも黒砂糖、赤砂糖、三温
糖が好ましい。Next, the amount of one or more insecticidal compounds selected from Table 1 and Table 2 of the group consisting of insecticidal compounds depends on the type of compound and the type of target pest, but usually, The amount is 0.01 to 2.0% by weight based on the total amount of poison bait. A representative example of the crystalline cellulose is Avicel manufactured by Asahi Kasei Industries, Ltd., and the amount used is usually 20.0 to 60.0% by weight based on the total amount of the poison bait. Examples of grain powders include starch flours such as potatoes, sweet potatoes, and corn, and grain flours such as wheat flour, rice flour, and corn flour, and the amount used is usually 10.0% of the total amount of poison bait.
~80.0% by weight. Preferred examples of plant essential oils include soybean oil, rapeseed oil, sesame oil, and wheat germ oil. ,
Examples include glucose, fructose, lactose, brown sugar, brown sugar, and brown sugar, among which brown sugar, brown sugar, and brown sugar are preferred.
なお、この発明の害虫駆除用毒餌剤においては、必要に
応じて酸化防止剤、保存料、誤食防止剤、その他害虫に
対する誘引性を増強するための香料などを添加してもよ
い。ここで、酸化防止剤としては、たとえば、エリソル
ビン酸、エリソルビン酸ナトリウム、ジブチルヒドロキ
シトルエン、dl−α−トコフェロール、ノルジヒドロ
グアヤレチック酸、メチルヒドロキシアニソール、没食
子酸プロピル、グアヤク脂、L−システィン塩酸塩など
が挙げられ、保存料としては、たとえば、安息香酸、安
息香酸ナトリウム、サリチル酸、ジフェニル、ソルビン
酸、ソルビン酸カリウム、デヒドロ酢酸、デヒドロ酢酸
ナトリウム、パラオキシ安息香酸イソブチル、パラオキ
シ安息香酸イソプロピル、パラオキシ安息香酸エチル、
パラオキシ安息香酸ブチル、パラオキシ安息香酸プロピ
ル、プロピオン酸カルシウム、プロピオン酸ナトリウム
などを挙げることが出来る。また誤食防止剤としては、
たとえば、トウガラシ末、アマランス、アマランスアル
ミニウムレーキ、エリスロシン、エリスロシンアルミニ
ウムレーキ、ニューコクシン、フロキシン、ローズベン
ガル、アシドレッド、タートラジン、タートラジンアル
ミニウムレーキ、サンセットイエローFCF 、サンセ
ットイエローFCFアルミニウムレーキ、ファストグリ
ーンFCF 。In addition, in the poison bait for controlling pests of the present invention, antioxidants, preservatives, agents to prevent accidental ingestion, and other fragrances to enhance attractivity to pests may be added as necessary. Here, as the antioxidant, for example, erythorbic acid, sodium erythorbate, dibutylhydroxytoluene, dl-α-tocopherol, nordihydroguaiaretic acid, methylhydroxyanisole, propyl gallate, guaiac butter, L-cystine hydrochloride Examples of preservatives include benzoic acid, sodium benzoate, salicylic acid, diphenyl, sorbic acid, potassium sorbate, dehydroacetic acid, sodium dehydroacetate, isobutyl paraoxybenzoate, isopropyl paraoxybenzoate, and paraoxybenzoate. ethyl acid,
Examples include butyl paraoxybenzoate, propyl paraoxybenzoate, calcium propionate, sodium propionate, and the like. In addition, as an agent to prevent accidental ingestion,
For example, capsicum powder, amaranth, amaranth aluminum lake, erythrosine, erythrosine aluminum lake, newcoxin, phloxine, rose bengal, acid red, tartrazine, tartrazine aluminum lake, sunset yellow FCF, sunset yellow FCF aluminum lake, fast green FCF .
ファストグリーンFCFアルミニウムレーキ、ブリリア
ントブルーFCF 、ブリリアントブルーFCFアルミ
ニウムレーキ、インジゴカルミン、インジゴカルミンア
ルミニウムレーキ、β−カロチン、銅クロロフィルなど
が挙げられる。また、香料としてはたとえばチーズ香料
、バター香料、ビーナツツ香料、ビーチ香料、ストロベ
リー香料、ミルク香料などを例示することが出来る。Examples include fast green FCF aluminum lake, brilliant blue FCF, brilliant blue FCF aluminum lake, indigo carmine, indigo carmine aluminum lake, β-carotene, copper chlorophyll, and the like. Examples of the flavor include cheese flavor, butter flavor, peanut flavor, beach flavor, strawberry flavor, milk flavor, and the like.
以上の有効成分および必要に応じて加えられる添加物を
製剤するにあたっては、特に限定するものではないが、
殺虫性化合物と植物精油とを予め室温もしくは加温した
状態下で混合し、これを糖、結晶セルロース、穀類粉末
およびその他物賞と均一に混合した後、常法に従って任
意の大きさに打錠成形すればよい。In formulating the above active ingredients and additives added as necessary, there are no particular limitations, but
The insecticidal compound and the plant essential oil are mixed in advance at room temperature or in a heated state, and this is mixed uniformly with sugar, crystalline cellulose, grain powder, and other substances, and then tableted into any size according to a conventional method. Just mold it.
この発明の毒餌剤は、ワモンゴキブリ、チャバネゴキブ
リ、クロゴキブリ等のゴキブリ類、ヒメアリ、クロヤマ
了り等のアリ類、タバコシバンムシ、ジンサンシバンム
シ等のシバンムシ類、コクヌストモドキ、ヒラタコクヌ
ストモドキ等のゴミムシダマシ類、ノコギリとラタムシ
、カクムネヒラタムシ等のヒラタムシ類などの害虫駆除
剤として使用できる。The poisonous bait of this invention is suitable for cockroaches such as the American cockroach, German cockroach, and black cockroach; ants such as the American cockroach, German cockroach, and black cockroach; It can be used as an exterminator for insect pests such as Latam beetles and hirata beetles.
実施例1〜6:
ピリブロキシフエン0.05%(%は重量%、以下同じ
)、結晶セルロース30.0%、ゴマ油3.0%、ブチ
ルヒドロキシアニソール0.03%およびデしドロ酢酸
0.1%に対して第3表に示すような割合で糖およびジ
ャガイモデンプンを配合した。まずビリプロキシフェン
とゴマ油とを混合し、これに糖、結晶セルロース、ジャ
ガイモデンプン、ブチルヒドロキシアニソールおよびデ
ヒドロ酢酸を加え、均一に混合した後、15にぎ/cd
の圧力をかけ、1錠約4g(径約30fl)に打錠成形
し、毒餌剤を得た。得られた毒餌剤に対して、有効成分
の安定性、ゴキブリに対する誘引喫食効果、羽化阻害効
果および産卵抑制効果を評価した。その評価方法第
3 表
幹:tI(財)
はつぎのとおりである。Examples 1 to 6: 0.05% pyribroxifene (% is weight %, the same applies hereinafter), 30.0% crystalline cellulose, 3.0% sesame oil, 0.03% butylhydroxyanisole, and 0 dedroacetic acid. Sugar and potato starch were blended in the proportions shown in Table 3 relative to .1%. First, mix biliproxyfen and sesame oil, add sugar, crystalline cellulose, potato starch, butylhydroxyanisole, and dehydroacetic acid, mix uniformly, and add 15 min/cd.
The mixture was compressed into tablets of about 4 g (diameter: about 30 fl) by applying a pressure of The obtained poisonous bait was evaluated for the stability of the active ingredient, the effect of attracting and eating cockroaches, the effect of inhibiting emergence, and the effect of suppressing spawning. Evaluation method No.
3 Main stem: tI (goods) is as follows.
■ 有効成分の安定性:
毒餌剤を50℃のちとに10日間保持した後、有効成分
の残存率をガスクロマトグラフィーを用いて算出し、残
存率の80%以上(○印)と80%未満(×印)との二
段階評価を行なった。■ Stability of active ingredients: After keeping the poison bait at 50℃ for 10 days, the residual rate of the active ingredient was calculated using gas chromatography, and the residual rate was 80% or more (○ mark) or less than 80%. A two-level evaluation was performed with (x mark).
■ 誘引喫食効果:
底面積0.12rdの容器にチャバネゴキブリ成虫50
匹(雌雄同数)を入れ、その中に検体と対照餌とを配置
し、一定時間内に誘引された供試虫数から検体の誘引率
を算出し、誘引率の70%以上(+印)と70%未満(
−印)との二段階評価を行なった。■ Attractive eating effect: 50 adult German cockroaches in a container with a bottom area of 0.12rd.
(same number of males and females), place the specimen and control bait inside it, and calculate the attraction rate of the specimen from the number of test insects attracted within a certain time, and calculate the attraction rate of the specimen by 70% or more (+ mark). and less than 70% (
A two-level evaluation was conducted with - marks).
■ 羽化阻害効果:
底面積100−の容器にチャバネゴキブリ終齢幼虫lO
匹(雌雄同数)を入れ、この中に検体と対照餌とを配置
し、その後定期的に成虫への羽化状況を観察した。3週
間経過後、羽化失敗、翅の異常、適齢幼虫の数の割合が
80%以上(+−)と80%未満(−印)との二段階評
価を行なった。■ Inhibitory effect on emergence: 10 German cockroach final instar larvae in a container with a base area of 100
The specimen and control food were placed inside the specimen (equal number of males and females), and the status of emergence into adults was then periodically observed. After 3 weeks, a two-tiered evaluation was performed: failure to emerge, wing abnormalities, and number of suitable larvae were 80% or more (+-) and less than 80% (-).
■ 産卵抑制効果:
底面積10G−の容器に羽化−週間以内のチ中バネゴキ
ブリ10匹(雌雄同数)を入れ、この中に検体と対照餌
とを配置し、その後定期的に産卵数およびフ化率を観察
した。4週間経過後、無処理区に対する次世代の増殖抑
制率が80%以上(+−)と80%未満(−印)との二
段階評価を行なった。■ Egg-laying suppression effect: Place 10 medium-sized spring cockroaches (equal numbers of males and females) within a week of emergence into a container with a bottom area of 10 G, place the specimen and control food inside the container, and then periodically measure the number of eggs laid and the number of eggs laid. The conversion rate was observed. After 4 weeks, the next generation growth inhibition rate was evaluated in two stages: 80% or more (+-) and less than 80% (- mark) relative to the untreated plot.
以上の評価結果を第4表にまとめた。The above evaluation results are summarized in Table 4.
比較例1〜4:
第5表のように糖の量を限定範囲未満とし、その分ジャ
ガイモデンプンを増量したこと以外は実施例1と全く同
様の操作を行ない、毒餌剤を調製し、諸効果を調べた。Comparative Examples 1 to 4: As shown in Table 5, the amount of sugar was kept below the limited range and the amount of potato starch was increased accordingly. I looked into it.
得られた結果を第5表に併第 4 表 記した。The obtained results are included in Table 5 Table 4 I wrote it down.
第3表、第4表および第5表から明らかなように、糖を
全く加えないとき(比較例1)また限定量未満のとき(
比較例2〜4)はいずれも有効成分の安定性について大
きい相違は認め、られなくても、誘引喫食効果、羽化阻
害効果および産卵抑制効果においては実施例1〜6のい
ずれよりもかなり劣ワていた。As is clear from Tables 3, 4 and 5, when no sugar is added at all (Comparative Example 1) and when the amount is less than the limited amount (
Comparative Examples 2 to 4) all showed a large difference in the stability of the active ingredients, and even if there was no difference, they were significantly inferior to any of Examples 1 to 6 in terms of attracting feeding effect, eclosion inhibition effect, and spawning inhibition effect. was.
実施例7〜9:
結晶セルロース30.0%、三温糖10.0%、プチル
ヒドロオキシアニゾール0.03%、デヒドロ酸90.
10%のほかに第6表に示すような成分を配合し、実施
例1と全く同様の操作を行ない毒餌剤を調製し、その諸
効果を調べ得られた結果を第6表に併記した。Examples 7 to 9: 30.0% crystalline cellulose, 10.0% brown sugar, 0.03% butylhydroxyanisole, 90% dehydroic acid.
In addition to 10%, the ingredients shown in Table 6 were blended and the same operations as in Example 1 were carried out to prepare a poisonous bait.The various effects thereof were investigated and the results obtained are also listed in Table 6.
比較例5〜7:
第6表に併記したように植物精油を全く用いなかったこ
とおよびそれに伴ってジャガイモデンプンの量をやや増
加したこと以外は実施例7〜9と全く同様の操作を行な
って毒餌剤を調製し、その諸効果を調べた。得られた結
果を第6表に併記したが、比較例5〜7はいずれも安定
性、誘引効果、羽化阻害効果および産卵抑制効果のすべ
ての点で劣っていた。Comparative Examples 5-7: As shown in Table 6, the same operations as Examples 7-9 were performed except that no vegetable essential oil was used and the amount of potato starch was slightly increased accordingly. We prepared poisonous baits and investigated their effects. The obtained results are also listed in Table 6, and Comparative Examples 5 to 7 were all inferior in all aspects of stability, attraction effect, emergence inhibition effect, and spawning inhibition effect.
実施例10〜15:
第7表に示した成分を配合(数字は重量%)し、実施例
1と同様の操作を行なって毒餌剤を調製し、それぞれの
諸効果を測定した。得られた結果を第7表に併記したが
、安定性、誘引効果、羽化阻害効果および産卵抑制効果
はすべて良好であった。Examples 10 to 15: The ingredients shown in Table 7 were blended (numbers are weight %), the same operations as in Example 1 were performed to prepare poison baits, and the various effects of each were measured. The obtained results are also listed in Table 7, and the stability, attraction effect, emergence inhibition effect, and spawning inhibition effect were all good.
(以下余白)
第 7 表
〔効果〕
以上述べたことから明らかなように、この発明の害虫駆
除用毒餌剤は、有効成分の安定性、害虫特にゴキブリに
対しても誘引喫食効果、羽化阻害効果、産卵抑制効果お
よび取扱い上の安全性において、従来品よりも皇かに優
れたものであり、また、製剤としてのひび割れまたは崩
壊の問題もないことから、ゴキブリなどの害虫駆除用毒
餌剤として有用である。(The following is a blank space) Table 7 [Effects] As is clear from the above, the poison bait for exterminating pests of the present invention has the stability of the active ingredient, the effect of attracting insects, especially cockroaches, and the effect of inhibiting their emergence. It is much superior to conventional products in terms of its egg-laying suppressing effect and safety in handling, and there is no problem of cracking or disintegration as a formulation, making it useful as a poisonous bait for controlling pests such as cockroaches. It is.
特許出願人 住友化学工業株式会社 同 代理人 鎌 1) 文 二Patent applicant: Sumitomo Chemical Co., Ltd. Same agent Kama 1) Letter 2
Claims (1)
合物からなる群の中から選ばれる1種以上の昆虫成長制
御剤、結晶セルロース、穀類粉、さらに毒餌剤全量に対
し、0.1〜10.0重量%の植物精油および10.0
〜40.0重量%の糖を主要成分とし打錠されたことを
特徴とする害虫駆除用毒餌剤。0.1 to 10.0 weight of one or more insect growth regulators selected from the group consisting of insect juvenile hormone-like compounds and insect chitin formation inhibiting compounds, crystalline cellulose, grain flour, and the total amount of poison bait. % plant essential oil and 10.0
A poisonous bait for pest control, characterized in that it contains ~40.0% by weight of sugar as a main component and is compressed into a tablet.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62304142A JP2585319B2 (en) | 1987-11-30 | 1987-11-30 | Poison bait for pest control |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62304142A JP2585319B2 (en) | 1987-11-30 | 1987-11-30 | Poison bait for pest control |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01143806A true JPH01143806A (en) | 1989-06-06 |
JP2585319B2 JP2585319B2 (en) | 1997-02-26 |
Family
ID=17929550
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62304142A Expired - Fee Related JP2585319B2 (en) | 1987-11-30 | 1987-11-30 | Poison bait for pest control |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2585319B2 (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2231798A (en) * | 1989-05-27 | 1990-11-28 | Sumitomo Chemical Co | A poison bait for control of noxious insects |
FR2647305A1 (en) * | 1989-05-27 | 1990-11-30 | Sumitomo Chemical Co | APPAT EMPOESNE FOR THE FIGHT AGAINST PEST INSECTS |
US5707640A (en) * | 1993-09-20 | 1998-01-13 | Nihon Bayer Agrochem K.K. | Poisonous baits for controlling soil-inhabiting pests |
WO1998034481A1 (en) * | 1997-02-12 | 1998-08-13 | Dow Agrosciences Llc | Synergistic juvenoid/chitin synthesis inhibitor termiticide compositions |
FR2798042A1 (en) * | 1999-09-07 | 2001-03-09 | Aventis Cropscience Sa | INSECTICIDAL COMPOSITIONS IN WHICH THE ACTIVE MATERIAL IS OF THE PHENYL-PYRAZOLE TYPE AND PROCESS FOR THE CONTROL OF SOIL INSECTS |
JP2001233712A (en) * | 1999-12-14 | 2001-08-28 | Nippon Kayaku Co Ltd | Insect pest controlling agent |
JP2005517027A (en) * | 2002-01-29 | 2005-06-09 | ホイットマイアー マイクロ−ゲン リサーチ ラボラトリーズ,インコーポレーテッド | Optimal density termite poison bait composition |
WO2005094578A1 (en) | 2004-03-29 | 2005-10-13 | Dow Agrosciences Llc | Pesticide compositions |
JP2007529557A (en) * | 2004-03-19 | 2007-10-25 | ダウ アグロサイエンシィズ エルエルシー | Insecticide composition |
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---|---|---|---|---|
JPS5391140A (en) * | 1977-01-20 | 1978-08-10 | Kao Corp | Attractants for cockroaches |
JPS60181062A (en) * | 1984-02-29 | 1985-09-14 | Nippon Soda Co Ltd | Alkenyl carbamate derivative, its preparation and insecticide |
JPS61268602A (en) * | 1985-05-13 | 1986-11-28 | サンド・アクチエンゲゼルシヤフト | Novel composition and method for controlling cockroach |
JPS62195301A (en) * | 1986-02-20 | 1987-08-28 | Yuui Katori Kk | Poisonous bait for cockroach |
JPS63218605A (en) * | 1987-03-06 | 1988-09-12 | Yuukou Yakuhin Kogyo Kk | Poisonous bait for extermination of vermin |
-
1987
- 1987-11-30 JP JP62304142A patent/JP2585319B2/en not_active Expired - Fee Related
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
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JPS5391140A (en) * | 1977-01-20 | 1978-08-10 | Kao Corp | Attractants for cockroaches |
JPS60181062A (en) * | 1984-02-29 | 1985-09-14 | Nippon Soda Co Ltd | Alkenyl carbamate derivative, its preparation and insecticide |
JPS61268602A (en) * | 1985-05-13 | 1986-11-28 | サンド・アクチエンゲゼルシヤフト | Novel composition and method for controlling cockroach |
JPS62195301A (en) * | 1986-02-20 | 1987-08-28 | Yuui Katori Kk | Poisonous bait for cockroach |
JPS63218605A (en) * | 1987-03-06 | 1988-09-12 | Yuukou Yakuhin Kogyo Kk | Poisonous bait for extermination of vermin |
Cited By (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2231798A (en) * | 1989-05-27 | 1990-11-28 | Sumitomo Chemical Co | A poison bait for control of noxious insects |
FR2647305A1 (en) * | 1989-05-27 | 1990-11-30 | Sumitomo Chemical Co | APPAT EMPOESNE FOR THE FIGHT AGAINST PEST INSECTS |
US5096710A (en) * | 1989-05-27 | 1992-03-17 | Sumitomo Chemical Company, Limited | Poison bait for control of noxious insects |
GB2231798B (en) * | 1989-05-27 | 1992-07-08 | Sumitomo Chemical Co | A poison bait for control of noxious insects |
ES2033170A1 (en) * | 1989-05-27 | 1993-03-01 | Sumitomo Chemical Co | Poison bait for control of noxious insects |
US5707640A (en) * | 1993-09-20 | 1998-01-13 | Nihon Bayer Agrochem K.K. | Poisonous baits for controlling soil-inhabiting pests |
US5882670A (en) * | 1993-09-20 | 1999-03-16 | Nihon Bayer Agrochem K.K. | Poisonous baits for controlling soil-inhabiting pests |
WO1998034481A1 (en) * | 1997-02-12 | 1998-08-13 | Dow Agrosciences Llc | Synergistic juvenoid/chitin synthesis inhibitor termiticide compositions |
FR2798042A1 (en) * | 1999-09-07 | 2001-03-09 | Aventis Cropscience Sa | INSECTICIDAL COMPOSITIONS IN WHICH THE ACTIVE MATERIAL IS OF THE PHENYL-PYRAZOLE TYPE AND PROCESS FOR THE CONTROL OF SOIL INSECTS |
WO2001017354A1 (en) * | 1999-09-07 | 2001-03-15 | Aventis Cropscience Sa | Method for fighting soil insects with phenyl-pyrazoles |
JP2001233712A (en) * | 1999-12-14 | 2001-08-28 | Nippon Kayaku Co Ltd | Insect pest controlling agent |
JP4603679B2 (en) * | 1999-12-14 | 2010-12-22 | 日本化薬株式会社 | Pest control agent |
JP2005517027A (en) * | 2002-01-29 | 2005-06-09 | ホイットマイアー マイクロ−ゲン リサーチ ラボラトリーズ,インコーポレーテッド | Optimal density termite poison bait composition |
US8720108B2 (en) | 2002-01-29 | 2014-05-13 | Basf Corporation | Optimum density termite bait composition |
US10334835B2 (en) | 2002-01-29 | 2019-07-02 | Basf Corporation | Method for preparing an optimum density termite bait composition |
JP2007529557A (en) * | 2004-03-19 | 2007-10-25 | ダウ アグロサイエンシィズ エルエルシー | Insecticide composition |
WO2005094578A1 (en) | 2004-03-29 | 2005-10-13 | Dow Agrosciences Llc | Pesticide compositions |
EP1729574A4 (en) * | 2004-03-29 | 2010-06-16 | Dow Agrosciences Llc | Pesticide compositions |
US7820189B2 (en) | 2004-03-29 | 2010-10-26 | Dow Agrosciences Llc | Pesticide compositions |
US8021675B2 (en) | 2004-03-29 | 2011-09-20 | Dow Agrosciences Llc | Pesticide compositions |
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