JPH0528682B2 - - Google Patents

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Publication number
JPH0528682B2
JPH0528682B2 JP59266738A JP26673884A JPH0528682B2 JP H0528682 B2 JPH0528682 B2 JP H0528682B2 JP 59266738 A JP59266738 A JP 59266738A JP 26673884 A JP26673884 A JP 26673884A JP H0528682 B2 JPH0528682 B2 JP H0528682B2
Authority
JP
Japan
Prior art keywords
parts
insecticidal
acaricidal
composition
present
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
Application number
JP59266738A
Other languages
Japanese (ja)
Other versions
JPS61145106A (en
Inventor
Masayoshi Hirose
Kiminori Hirata
Yasuhisa Hyodo
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.)
Nissan Chemical Corp
Original Assignee
Nissan Chemical Corp
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 Nissan Chemical Corp filed Critical Nissan Chemical Corp
Priority to JP59266738A priority Critical patent/JPS61145106A/en
Publication of JPS61145106A publication Critical patent/JPS61145106A/en
Publication of JPH0528682B2 publication Critical patent/JPH0528682B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は、特定のピリタジノン誘導体と、公知
の殺虫剤および/または殺ダニ剤の有効成分化合
物とを混合してなることを特徴とする殺虫・殺ダ
ニ剤組成物に関するものである。 今日、農園芸用害虫、森林害虫あるいは衛生害
虫等各種害虫の防除を目的とする殺虫・殺ダニ剤
の開発が広く進められ、多種多様な薬剤が実用に
供されている。しかしながら、人畜あるいは魚類
に対する毒性、殺虫・殺ダニスペクトラム、殺
虫・殺ダニ効果およびその残効性などのすべてを
満足する薬剤が要望されているが、これらすべて
満足することは難しい。 本発明者らは、これら既存の薬剤に比べてより
殺虫・殺ダニ特性のすぐれた殺虫・殺ダニ剤の開
発をすべく検討を進める中で、新しい作用性の殺
虫・殺ダニ剤である特定のピリダジノン誘導体
と、既存の殺虫・殺ダニ剤の有効成分化合物とを
組み合わせた本発明殺虫・殺ダニ組成物がすぐれ
た共力的殺虫効果を有することを見出したもので
ある。すなはち、本発明は、式(): で表される化合物と、下記の〜で表される化
合物の少なくとも一種とを有効成分として、含有
する殺虫・殺ダニ剤に関するものである。
The present invention relates to an insecticidal/acaricide composition comprising a mixture of a specific pyritazinone derivative and an active ingredient compound of a known insecticide and/or acaricide. BACKGROUND OF THE INVENTION Today, the development of insecticides and acaricides for the purpose of controlling various pests such as agricultural and horticultural pests, forest pests, and sanitary pests is being widely advanced, and a wide variety of pesticides are in practical use. However, there is a demand for a drug that satisfies all of the following, including toxicity to humans, livestock, and fish, insecticidal/acaricidal spectrum, insecticidal/acaricidal effects, and residual efficacy, but it is difficult to satisfy all of these requirements. The present inventors, while proceeding with studies to develop insecticides and acaricides with superior insecticidal and acaricidal properties compared to these existing drugs, identified a new active insecticide and acaricide. It has been discovered that the insecticidal/acaricidal composition of the present invention, which is a combination of the pyridazinone derivative and the active ingredient compound of an existing insecticide/acaricide, has an excellent synergistic insecticidal effect. In other words, the present invention is based on the formula (): This invention relates to an insecticide/acaricide containing a compound represented by the following as active ingredients and at least one of the compounds represented by the following .

【表】【table】

【表】 本発明の殺虫・殺ダニ剤組成物の特徴点は、第
一に、各単剤の施用の場合に比し、その殺虫・殺
ダニ効力が明らかに増強されるとともに速効的な
殺虫・殺ダニ効果が付与されることであり、第二
に、既存の殺虫および/または殺ダニ剤にみられ
ない広い殺虫・殺ダニスペクトラムを有すること
と、長い残効性を兼ね備えていることである。す
なわち、本発明の殺虫・殺ダニ剤組成物は、共力
的殺虫・殺ダニ作用を有するものである。この共
力的殺虫・殺ダニ作用は各単剤の有する殺虫・殺
ダニ特性からは予測し得ぬ相乗効果に基づくもの
であり、本発明組成物の有用性は各種害虫に対す
る確実な防除効果、すなわち速効性に加うる残効
性も高いという長期持続的にそのすぐれた殺虫・
殺ダニ効力を発揮し得る点にあるといえる。 本発明の殺虫・殺ダニ組成物は、ツマグロヨコ
バイ等の半翅目害虫、コナガ等の鱗翅目害虫、鞘
翅目害虫、アカイエカ等の衛生害虫に卓越した殺
虫力を有するとともに、果樹および蔬菜に寄生す
る種々のダニ例えば、ナミハダニ、カンザワハダ
ニ、ニセナミハダニ、ミカンハダニ、リンゴハダ
ニ等および動物に寄生するダニ例えば、オウシマ
ダニ、ブーフイラス・アニユレイタス、アンブリ
オンマ・マクレイタム、リピセフアラス・アペン
デイクラータス、フタトゲチマダニ等の防除にも
有効である。 本発明の殺虫・殺ダニ組成物の施用にあたつて
は、一般には適当な担体と混用して適用すること
ができ所要の場合にはさらに乳化剤、分散剤、懸
濁剤、浸透剤、安定剤などを添加し乳剤、水和
剤、フロアブル剤、粉剤、粒剤、油剤、エアゾー
ル等任意の剤型にて実用に供することができる。
更に必要に応じて他種の殺虫剤、各種の殺菌剤、
除草剤、植物生長調整剤、共力剤、忌避剤、香料
などを添加して使用することもできる。 前記の式()で表されるピリタジノン系化合
物(以下、単に化合物Aという。)と他方の殺虫
および/または殺ダニ剤の有効成分化合物との混
合割合は、前者が1重量部に対して、一般的には
後者が0.01〜30重量部であるが、好ましくは0.01
〜20重量部がよい。 次に、本発明の殺虫・殺ダニ剤組成物の実施例
を具体的に挙げて示すが、もちろんこれらのみに
限定されるものではない。 以下の「部」はすべて重量部を示す。 配合例 1 乳剤 化合物A …5部 DMTP(一般名) …20部 キシロール …60部 ソルボール2680 …15部 (非イオン性界面活性剤とアニオン性界面活性
剤との混合物:東邦化学工業(株)商品名) 上記成分を均一に混合して乳剤とする。使用に
際しては上記乳剤を100〜2000倍に希釈して10ア
ールあたり50〜500を噴霧する。 配合例 2 水和剤 化合物A ………2部 酸化フエンブタスズ(一般名) ………10部 ジークライトPFP(カオリンナイトとセリサイ
トの混合物:ジークライト工業(株)商品名)
………79部 ソルボール5039(非イオン性界面活性剤とアニ
オン性界面活性剤との混合物:東邦化学工業(株)
商品名) ………4部 カーブレツクス#80(ホワイトカーボン:塩野
義製薬(株)商品名) ………3部 リグニンスルホン酸カルシウム ………2部 上記成分をジエツトエアーミルにて均一に混合
粉砕して水和剤とする。使用に際しては上記水和
剤を100〜2000倍に希釈して10アールあたり50〜
500を噴霧する。 配合例 3 フロアブル剤 化合物A ………5部 ビナパクリル(一般名) ………20部 ソルボール3353(非イオン性界面活性剤:東邦
化学工業(株)商品名) ………10部 ルノツクス1000c(陰イオン界面活性剤:東邦化
学工業(株)商品名) ………1部 1%ザンサンガム水溶液(天然高分子)
………20部 水 ………44部 有効成分を除く上記成分を均一に溶解し、つい
で有効成分を加えよく撹拌した後、サンドミルに
て湿式粉砕してフロアブル剤を得た。使用に際し
ては上記フロアブル剤を100〜2000倍に希釈して
10アールあたり50〜500を噴霧する。 配合例 4 粉砕 化合物A …0.5部 ケルセン(一般名) …2部 カーブレツクス#80(ホワイトカーボン:塩野
義製薬(株)商品名) …1部 ジークライトD(カオリンナイトとセリサイト
の混合物:ジークライト工業(株)商品名)…95部 リン酸ジイソプロピル …1.5部 上記成分を均一に混合粉砕して粉剤とする。使
用に際しては上記粉剤を10アールあたり1〜30Kg
散布する。 配合例 5 エアゾール 化合物A …0.5部 DDVP(一般名) …5部 キシレン …5部 脱臭灯油 …49.5部 上記成分を混合溶解し、エアゾール容器に充填
し、パイプ部分を取り付けた後に、そのバルブ部
分を通じて噴射剤(液化石油ガス)40部を加圧充
填しエアゾールを得る。 次に、本発明の殺虫・殺ダニ剤組成物が優れた
殺虫・殺ダニ作用を示すことを、具体的に試験例
を挙げて説明する。 試験例 1 カンザワハダニの成虫に対する殺虫効果試験 インゲンの葉をリーフパンチを用いて径1.5cm
の円形に切り取り、径7cmのスチロールカツプ上
の湿つた濾紙上に置いた。これにカンザワハダニ
の雌成虫を1葉あたり10頭接種した。接種半日後
に本発明組成物および対照単剤を水に分散させ所
定濃度に希釈した薬液をスチロールカツプあたり
2mlずつ回転式散布塔を用いて散布し25℃の照明
付き恒温室内に保存した。72時間経過後の死虫率
を下記の計算式から求めた。 死虫率(%)=死虫率/放虫数×100 この死虫率のデーターよりLC50値を求めた。
更に共力効果(相乗効果)の程度を判定するため
に通常用いられているSun and Johnson法〔ジ
ヤーナル・オブ・エコノミツク・エントモロジー
(J.Econ.Ent.)第53巻、887頁(1960年)〕の式を
用いて共力作用を判定した。対照の単剤のLC50
値は第1表に、本発明の組成物のLC50値および
共力係数は第2表に示す。なお、共力係数は下記
式で表される。(Sun and Johnson法による) 共力係数=混合剤の実際の毒性指数/混合剤の理論的
毒性指数×100 この値が100より大きいほど共力作用が強く100
に等しいときは相加作用、100より小さくなるほ
ど拮抗作用がある。 試験例 2 カンザワハダニに対するポツト試験 径20cmのポツトに茶を植えてカンザワハダニを
繁殖させた。散布直前にそれぞれの茶に寄生して
いるカンザワハダニの寄生虫数を調査し本発明組
成物および対照の単剤を水に分散させて所定濃度
に調整し、その薬液を上記ポツトの茶の莖葉に散
布した。風乾後、ポツトを温室に保存し、散布後
5日目・10日目・20日目・30日目にそれぞれの茶
に寄生しているカンザワハダニの寄生虫数を調査
した。 この結果を第3表に示す。 尚、指数は下記により計算した。 寄生指数=散布後の寄生雌成虫数/散布前の寄生雌成
虫数×100 試験例 3 ミカンハダニに対するポツト試験 径20cmのポツトに温州ミカンを植えて、ミカン
ハダニを繁殖させた。散布直前にそれぞれのミカ
ンに寄生しているミカンハダニの寄生虫数を調査
し、本発明組成物および対照の単剤を水に分散さ
せて所定濃度に調整し、その薬液を上記ポツトの
ミカンの莖葉に散布した。風乾後ポツトを温室に
保存し、散布後5日目・10日目・20日目・30日
目・40日目・50日目にそれぞれのミカンに寄生し
ているミカンハダニの寄生虫数を調査した。 この結果を第4表に示す。 尚、指数は下記により計算した。 寄生指数=散布後の寄生雌成虫数/散布前の寄生雌成
虫数×100 試験例 4 モモアカアブラムシに対する殺虫効力試験 1/10000アールのポツトにキヤベツを植えて
モモアカアブラムシを繁植させた。 本発明殺虫・殺ダニ剤組成物および対照の単剤
を水に分散させて所定濃度に調整し、その薬液を
上記ポツト中のキヤベツの莖葉に散布した。風乾
後、ポツトを保存し、散布後3日目にそれぞれの
キヤベツに寄生しているモモアカアブラムシの寄
生虫数を調査した。 この結果を第5表に示す。
[Table] The characteristics of the insecticidal/acaricidal composition of the present invention are, firstly, that its insecticidal/acaricidal efficacy is clearly enhanced compared to the case of applying each agent alone, and it is a fast-acting insecticidal agent. - It has acaricidal effect, and secondly, it has a wide insecticidal and acaricidal spectrum that is not found in existing insecticides and/or acaricides, and it has a long residual effect. be. That is, the insecticidal/acaricidal composition of the present invention has a synergistic insecticidal/acaricidal action. This synergistic insecticidal and acaricidal action is based on a synergistic effect that cannot be predicted from the insecticidal and acaricidal properties of each single agent, and the usefulness of the composition of the present invention is due to its reliable control effect against various pests, In other words, it is an excellent insecticidal agent with a long-lasting effect that is not only fast-acting but also has a high residual effect.
It can be said that it is capable of exhibiting acaricidal efficacy. The insecticidal/acaricidal composition of the present invention has excellent insecticidal power against Hemiptera pests such as leafhoppers, Lepidoptera pests such as the diamondback moth, Coleoptera pests, and sanitary pests such as Culex mosquito, and is parasitic on fruit trees and vegetables. It is also effective in controlling various mites, such as the two-spotted spider mite, Kanzawa spider mite, false red spider mite, citrus spider mite, apple spider mite, etc., and mites that parasitic on animals, such as the American spider mite, Bohuillus annullitas, Amblyomma maculatum, Lipicephalus appendiculatus, and the two-legged spider mite. . When applying the insecticidal/acaricidal composition of the present invention, it can generally be applied by mixing with a suitable carrier, and if necessary, emulsifying agents, dispersing agents, suspending agents, penetrating agents, stabilizing agents, etc. It can be put to practical use in any desired dosage form, such as emulsions, wettable powders, flowables, powders, granules, oils, aerosols, etc. by adding additives.
In addition, other types of insecticides, various fungicides,
It is also possible to add herbicides, plant growth regulators, synergists, repellents, fragrances, and the like. The mixing ratio of the pyritazinone compound represented by the above formula () (hereinafter simply referred to as compound A) and the other active ingredient compound of the insecticide and/or acaricide is as follows: Generally the latter is 0.01 to 30 parts by weight, preferably 0.01
~20 parts by weight is good. Next, specific examples of the insecticide/acaricide composition of the present invention will be shown, but of course the invention is not limited to these. All "parts" below indicate parts by weight. Formulation example 1 Emulsion compound A...5 parts DMTP (common name)...20 parts Xylene...60 parts Sorbol 2680...15 parts (mixture of nonionic surfactant and anionic surfactant: Toho Chemical Industry Co., Ltd. product) name) The above ingredients are mixed uniformly to form an emulsion. When using, the above emulsion is diluted 100 to 2000 times and sprayed at 50 to 500 per 10 ares. Formulation example 2 Wettable powder compound A: 2 parts fenbutastin oxide (common name): 10 parts Siegrite PFP (mixture of kaolinite and sericite: Sieglite Industries Co., Ltd. trade name)
…79 parts Solbol 5039 (mixture of nonionic surfactant and anionic surfactant: Toho Chemical Industry Co., Ltd.)
(Product name) ...4 parts Carbrex #80 (white carbon: Shionogi & Co., Ltd. product name) ...3 parts Calcium ligninsulfonate ...2 parts The above ingredients are mixed uniformly in a jet air mill. Grind and use as a hydrating agent. When using, dilute the above hydrating agent 100 to 2000 times and add 50 to 50 per 10 ares.
Spray 500. Formulation example 3 Flowable agent compound A......5 parts Binapacryl (generic name)......20 parts Sorbol 3353 (nonionic surfactant: Toho Chemical Industry Co., Ltd. trade name)......10 parts Lunox 1000c (hydrogen) Ionic surfactant: Toho Chemical Industry Co., Ltd. trade name) 1 part 1% xanthan gum aqueous solution (natural polymer)
20 parts Water 44 parts The above ingredients except the active ingredient were uniformly dissolved, and then the active ingredient was added and stirred thoroughly, followed by wet grinding in a sand mill to obtain a flowable agent. When using, dilute the above flowable agent 100 to 2000 times.
Spray 50-500 per 10 are. Formulation example 4 Grinding compound A...0.5 part Kelsen (generic name)...2 parts Carbrex #80 (white carbon: trade name of Shionogi & Co., Ltd.)...1 part Siegrite D (mixture of kaolinite and sericite: Sieglite) Kogyo Co., Ltd. (trade name)...95 parts Diisopropyl phosphate...1.5 parts The above ingredients are uniformly mixed and pulverized to form a powder. When using, add 1 to 30 kg of the above powder per 10 ares.
Spread. Formulation example 5 Aerosol compound A...0.5 parts DDVP (common name)...5 parts Xylene...5 parts Deodorized kerosene...49.5 parts Mix and dissolve the above ingredients, fill it into an aerosol container, and after attaching the pipe part, pour it through the valve part. 40 parts of propellant (liquefied petroleum gas) is charged under pressure to obtain an aerosol. Next, the fact that the insecticidal and acaricidal composition of the present invention exhibits excellent insecticidal and acaricidal effects will be specifically explained with reference to test examples. Test example 1 Insecticidal effect test against adult Kanzawa spider mites Green bean leaves were punched with a diameter of 1.5cm using a leaf punch.
A circle was cut out and placed on wet filter paper on a styrofoam cup with a diameter of 7 cm. This was inoculated with 10 female adult Kanzawa spider mites per leaf. Half a day after inoculation, the composition of the present invention and the control single agent were dispersed in water and diluted to a predetermined concentration, and 2 ml of the drug solution was sprayed per styrene cup using a rotary spray tower and stored in a constant temperature room with lighting at 25°C. The insect mortality rate after 72 hours was calculated using the following formula. Mortality rate (%) = Mortality rate/Number of insects released x 100 The LC 50 value was determined from this data on the mortality rate.
Furthermore, the Sun and Johnson method, which is commonly used to determine the degree of synergistic effect (J.Econ.Ent.), Vol. 53, p. 887 (1960) )] was used to determine the synergistic effect. Control single agent LC 50
The values are shown in Table 1, and the LC 50 values and synergy coefficients of the compositions of the invention are shown in Table 2. Note that the synergistic coefficient is expressed by the following formula. (Based on the Sun and Johnson method) Synergy coefficient = Actual toxicity index of mixture / Theoretical toxicity index of mixture x 100 The greater this value is than 100, the stronger the synergism 100
When it is equal to , there is an additive effect, and when it is less than 100, there is an antagonistic effect. Test Example 2 Pot test against Kanzawa spider mites Tea was planted in pots with a diameter of 20 cm to breed Kanzawa spider mites. Immediately before spraying, the number of Kanzawa spider mite parasites infesting each tea plant was investigated, and the composition of the present invention and the control single agent were dispersed in water to adjust to a predetermined concentration, and the chemical solution was applied to the leaves of the tea leaves in the pots. was dispersed. After air-drying, the pots were stored in a greenhouse, and the number of Kanzawa spider mite parasites infesting each tea plant was investigated on the 5th, 10th, 20th, and 30th day after spraying. The results are shown in Table 3. In addition, the index was calculated as follows. Parasitic index = Number of parasitic female adults after spraying / Number of parasitic female adults before spraying × 100 Test example 3 Pot test against orange spider mites Citrus oranges were planted in pots with a diameter of 20 cm, and orange spider mites were bred. Immediately before spraying, the number of citrus spider mite parasites infesting each tangerine was investigated, the composition of the present invention and the control single agent were dispersed in water, adjusted to a predetermined concentration, and the chemical solution was applied to the hus of the tangerine in the pot. Sprayed on the leaves. After air-drying, the pots were stored in a greenhouse, and the number of tangerine spider mite parasites infesting each tangerine was investigated on the 5th, 10th, 20th, 30th, 40th, and 50th day after spraying. did. The results are shown in Table 4. In addition, the index was calculated as follows. Parasitic index = Number of parasitic female adults after spraying / Number of parasitic female adults before spraying x 100 Test Example 4 Insecticidal efficacy test against green peach aphid Cabbage was planted in a 1/10000 are pot to allow green peach aphid to flourish. The insecticide/acaricide composition of the present invention and a single control agent were dispersed in water and adjusted to a predetermined concentration, and the chemical solution was sprayed on the cabbage leaves in the pot. After air-drying, the pots were stored, and the number of green peach aphids parasitizing each cabbage was investigated three days after spraying. The results are shown in Table 5.

【表】 LC50値とは、半数のダニが致死する濃度であ
る。
[Table] LC 50 value is the concentration that kills half of the ticks.

【表】【table】

【表】【table】

【表】【table】

【表】 尚、散布5日後は計算から除外
[Table] Note that 5 days after spraying is excluded from calculation.

【表】【table】

【表】【table】

Claims (1)

【特許請求の範囲】 1 式(): で表される化合物と、下記の〜で表される化
合物の少なくとも一種とを有効成分として、含有
する殺虫・殺ダニ剤。
[Claims] 1 Formula (): An insecticide/acaricide containing a compound represented by and at least one of the compounds represented by ~ below as active ingredients.
JP59266738A 1984-12-18 1984-12-18 Insecticide-acaricide composition Granted JPS61145106A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59266738A JPS61145106A (en) 1984-12-18 1984-12-18 Insecticide-acaricide composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59266738A JPS61145106A (en) 1984-12-18 1984-12-18 Insecticide-acaricide composition

Publications (2)

Publication Number Publication Date
JPS61145106A JPS61145106A (en) 1986-07-02
JPH0528682B2 true JPH0528682B2 (en) 1993-04-27

Family

ID=17435009

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59266738A Granted JPS61145106A (en) 1984-12-18 1984-12-18 Insecticide-acaricide composition

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Publication number Priority date Publication date Assignee Title
US5670504A (en) * 1995-02-23 1997-09-23 Merck & Co. Inc. 2,6-diaryl pyridazinones with immunosuppressant activity
DE19615976A1 (en) * 1996-04-22 1997-10-23 Basf Ag Means and methods for controlling harmful fungi
CN103053568B (en) * 2013-01-18 2014-06-04 安徽省农业科学院植物保护与农产品质量安全研究所 Compound insecticide for preventing rice planthoppers

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6117570A (en) * 1984-07-04 1986-01-25 Nissan Chem Ind Ltd Pyridazinone derivative, its preparation and insecticidal, miticidal and bactericidal agent

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6117570A (en) * 1984-07-04 1986-01-25 Nissan Chem Ind Ltd Pyridazinone derivative, its preparation and insecticidal, miticidal and bactericidal agent

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