JPH01238505A - Control agent of harmful animal - Google Patents

Control agent of harmful animal

Info

Publication number
JPH01238505A
JPH01238505A JP63065050A JP6505088A JPH01238505A JP H01238505 A JPH01238505 A JP H01238505A JP 63065050 A JP63065050 A JP 63065050A JP 6505088 A JP6505088 A JP 6505088A JP H01238505 A JPH01238505 A JP H01238505A
Authority
JP
Japan
Prior art keywords
group
compound
based compound
compounds
alkyl
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.)
Pending
Application number
JP63065050A
Other languages
Japanese (ja)
Inventor
Tadaaki Toki
土岐 忠昭
Kiyomitsu Yoshida
潔充 吉田
Osamu Imai
修 今井
Masayuki Morita
雅之 森田
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.)
Ishihara Sangyo Kaisha Ltd
Original Assignee
Ishihara Sangyo Kaisha 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 Ishihara Sangyo Kaisha Ltd filed Critical Ishihara Sangyo Kaisha Ltd
Priority to JP63065050A priority Critical patent/JPH01238505A/en
Publication of JPH01238505A publication Critical patent/JPH01238505A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a control agent having a wide control spectrum and a large control effect to harmful animals such as tetranychus urticae Koch and plutella maculipennis Curtis with a small amount of drug, containing a specific compound and one of organic phosphorus based compound and carbamate based compound, etc., as active ingredients. CONSTITUTION:A compound expressed by the formula [X1 and X2 is H, alkyl or alkoxy capable of having substituent (halogen, alkoxy, alkylthio, phenoxy and phenylthio), carboxyl or phenyl, etc.; X3 and X4 is H or alkyl; X2 and X3 are joined to form alkylene; Y1, Y2 and Z is O or S; R1 and R2 is alkyl] and at least one of organic phosphorus based compound, carbamate based compound, pyrethroid based compound, urea based compound, sulfone based compound or N-pyridylaniline based compound are contained as active ingredients. The control agent is preferably compounded 0.5-90wt.% active ingredients and used together with a pesticide adjuvant.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、一般式(I)で表わされる化合物と、他の特
定の化合物とを有効成分として含有する有害動物防除剤
に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a pest control agent containing a compound represented by general formula (I) and other specific compounds as active ingredients.

〔従来の技術〕[Conventional technology]

一般式(I) (式中、X、及びX、は、水素原子;ハロゲン原子、ア
ルコキシ基、アルキルチオ基、フェノキシ基、ハロゲン
置換フェノキシ基、フェニルチオ基もしくはハロゲン置
換フェニルチオ基で置換されてもよいアルキル基或いは
アルコキシ基;カルホキシル基;アルコキシカルボニル
基;又はハロゲン原子で置換されてもよいフェニル基で
あり、Xt及びX4は水素原子又はアルキル基であり、
Xl及びX、は−猪になりアルキレン基を形成してもよ
く、Yl 、yz及びZは酸素原子又は硫黄原子であり
、R1及びR2はアルキル基である)で表わされる化合
物が有害な昆虫類、ダニ類、線虫類などに対して防除効
果を示すことはヨーロッパ特許公開第146,748号
公報により知られており、一方、他の特定の化合物につ
いても、有害動物防除剤として有効であることは公知で
ある。
General formula (I) (wherein, X and or an alkoxy group; a carboxyl group; an alkoxycarbonyl group; or a phenyl group which may be substituted with a halogen atom, and Xt and X4 are a hydrogen atom or an alkyl group,
Xl and It is known from European Patent Publication No. 146,748 that it exhibits a control effect against mites, nematodes, etc., and on the other hand, other specific compounds are also effective as pest control agents. This is well known.

〔発明の経緯〕[Background of the invention]

前記一般式(I)で表わされる化合物は一般に、線虫類
に対して高い防除効果を示すものの昆虫類、ダニ類など
についてはそれほど高い防除効果を示さない場合があり
、また有機リン系化合物、カーバメート系化合物、ピレ
スロイド系化合物、ウレア系化合物、スルフォン系化合
物又はN−ピリジルアニリン系化合物は施用場面によっ
ては、有害動物に対し実用上不十分な防除効果しか示さ
ないことがある。
Although the compound represented by the general formula (I) generally has a high control effect on nematodes, it may not have such a high control effect on insects, mites, etc., and organic phosphorus compounds, Carbamate-based compounds, pyrethroid-based compounds, urea-based compounds, sulfone-based compounds, or N-pyridylaniline-based compounds may exhibit only a practically insufficient control effect against harmful animals depending on the application situation.

本発明者達は前記一般式(I)で表わされる化合物に対
し、特定の化合物を混用施用することにより、各薬剤を
単独で施用した場合に比し相乗的な防除効果を示して薬
量を減少させたり或いは防除スペクトラムを拡大させた
りする効果が得られるため、各薬剤の施用場面が拡大す
ることの知見を得た。
The present inventors have demonstrated that by applying a specific compound to the compound represented by the general formula (I), a synergistic control effect can be obtained compared to when each agent is applied alone, and the dosage can be reduced. It was found that the application situations of each drug will be expanded because the effects of reducing the number of pests and expanding the control spectrum can be obtained.

(発明の開示〕 本発明は、一般式; (式中、Xl及びX、は、水素原子;ハロゲン原子、ア
ルコキシ基、アルキルチオ基、フェノキシ基、ハロゲン
置換フェノキシ基、フェニルチオ基もしくはハロゲン置
換フェニルチオ基で一置換されてもよいアルキル基或い
はアルコキシ基;カルボキシル基;アルコキシカルボニ
ル基;又はハロゲン原子で置換されてもよいフェニル基
であり・Xt及びX4は水素原子又はアルキル基であり
、Xz及びX、は−緒になりアルキレン基を形成シても
よく、Y + 、Y を及びZは酸素原子又は硫黄原子
であり、R2及びRiはアルキル基である)で表わされ
る化合物とを機リン系化合物、カーバメート系化合物、
ピレスロイド系化合物、ウレア系化合物、スルフォン系
化合物又はN−ピリジルアニリン系化合物の少なくとも
一種とを有効成分として含有する有害動物防除剤である
(Disclosure of the Invention) The present invention relates to the general formula; An alkyl group or an alkoxy group that may be monosubstituted; a carboxyl group; an alkoxycarbonyl group; or a phenyl group that may be substituted with a halogen atom. Xt and X4 are hydrogen atoms or alkyl groups, and Xz and X are - A compound represented by Y + , Y and Z are oxygen atoms or sulfur atoms, and R2 and Ri are alkyl groups) may be combined with a phosphorus-based compound, a carbamate. system compounds,
This is a pest control agent containing at least one of a pyrethroid compound, a urea compound, a sulfone compound, or an N-pyridylaniline compound as an active ingredient.

前記一般式(I)で表わされる化合物としては、例えば
、下記のようなものが挙げられる。
Examples of the compound represented by the general formula (I) include the following.

第1表 συ 上記第1表中、化合物りが同番号のaとb;a−
1とb−1、b−「;又はa−■とb−1,b−■;広
互いにジアステレオマーの関係にあり、またa−■とa
−■又はb−tとb−nは互いに鏡像異性体の関係にあ
る。
Table 1 συ In Table 1 above, compounds a and b with the same number; a-
1 and b-1, b-"; or a-■ and b-1, b-■; have a wide diastereomeric relationship with each other, and a-■ and a
-■ or b-t and b-n are enantiomers of each other.

表中の(fi)、 (i)、 (S)及び(t)1叡各
々ノルマル、イン、セカンダリ−及びターシャリ−の略
号である。
(fi), (i), (S) and (t)1 in the table are abbreviations for normal, in, secondary and tertiary, respectively.

また前記一般式(I)で表わされる化合物の混合相手薬
剤の前記有機リン系化合物としては、例えば、下記のも
のが挙げられる。
Further, examples of the organic phosphorus compounds to be mixed with the compound represented by the general formula (I) include the following.

第2表 前記カーバメート系化合物としては、例えば、下記のも
のが挙げられる。
Examples of the carbamate compounds in Table 2 include the following.

第3表 前記ピレスロイド系化合物としては、例えば、下記のも
のが挙げられる。
Examples of the pyrethroid compounds in Table 3 include the following.

第4表 前記ウレア系化合物、スルフォン系化合物又はN−ピリ
ジルアニリン系化合物としては、例えば、それぞれ下記
のものが挙げられる。
Table 4 Examples of the urea compounds, sulfone compounds, and N-pyridylaniline compounds include the following.

第5表 本発明薬剤の対象とする存置動物は、例えば、ナミハダ
ニ、ニセナミハダニ、ミカンハダニ、ネダニなどの植物
寄生性ダニ類、コナガ、ヨトウムシ、ハスモンヨトウ、
コドリンガ、ボールワーム、タバコバッドワーム、マイ
マイガ、コロラドハムシ、ウリハムシ、ポールウイービ
ル、アブラムシ類、ウンカ類、ヨコバイ類、カイガラム
シ類、カメムシ類、コナジラミ類、アザミウマ類、バッ
タ類、ハチバエ類、コガネムシ類、タマナヤガ、カブラ
ヤガ、タマネギバエ、タネバエ、アリ類などの農業害虫
類、イエダニ、ゴキブリ類、イエバエ・アカイエカなど
の衛生害虫類、バクガ、アズキゾウムシ、コクヌストモ
ドキ、ゴミムシダマシ類などの貯穀害虫類、イガ、ヒメ
力ツオプシムシ、シロアリ類などの衣類、家屋害虫類、
その他家畜などに寄生するノミ類、シラミ類、ハエ類な
どの防除に有効であり、更にはネコブセンチェウ類、シ
ストセンチュウ類、ネグザレセンチュウ類、イネシンガ
レセンチュウ、イチゴメセンチュウ、マツノザイセンチ
ユウなどの植物寄生性腺生類、またナメクジ、マイマイ
などの腹足類、ダンゴムシ、ワラジムシなどの等廖類が
あげられる6本発明の有害動物防除剤は、優れた浸透移
行性を有しているので、土壌に処理することによって土
壌有害昆虫類、ダニ類、線虫類、腹足類、等脚類の防除
と同時に茎葉部に生息する害虫類をも防除することがで
きる。
Table 5: Animals targeted by the drug of the present invention include, for example, plant parasitic mites such as two-spotted spider mites, false two-spotted spider mites, orange spider mites, and bed mites, diamondback moths, armyworms, fall armyworms,
Codling moth, ballworm, tobacco budworm, gypsy moth, Colorado potato beetle, cucumber beetle, poleweed beetle, aphids, planthoppers, leafhoppers, scale insects, stink bugs, whiteflies, thrips, grasshoppers, wasp flies, scarabs, Agricultural pests such as the snail moth, turnip weevil, onion fly, seed fly, and ants; sanitary pests such as dust mites, cockroaches, house fly, and Culex mosquito; grain storage pests such as the dust moth, adzuki bean weevil, white bean weevil, and mealworm; Clothes, house pests such as black beetles and termites,
It is also effective in controlling fleas, lice, flies, etc. that parasitize livestock, etc., as well as cat nematodes, cyst nematodes, nematode nematodes, rice nematodes, strawberry nematodes, pine tree nematodes, etc. The pest control agent of the present invention has excellent permeability, so it can be applied to the soil. By doing so, it is possible to control insects harmful to the soil, mites, nematodes, gastropods, and isopods, and at the same time, pests living in the stems and leaves can be controlled.

本発明の有害動物防除剤を使用するに際しては、従来の
農薬の製剤の場合と同様に農薬補助剤と共に乳剤、粉剤
、粒剤、水和剤、液剤、エアゾール剤、ペースト剤など
の種々の形態に製剤することができる、これらの配合割
合は通常有効成分0.5〜90重量部で農薬補助剤10
〜99.5重量部である。
When using the pest control agent of the present invention, it can be used in various forms such as emulsions, powders, granules, wettable powders, liquids, aerosols, pastes, etc., together with pesticide auxiliaries, as in the case of conventional pesticide formulations. The compounding ratio of these ingredients is usually 0.5 to 90 parts by weight of the active ingredient and 10 parts by weight of the agricultural chemical adjuvant.
~99.5 parts by weight.

これらの製剤の実際の使用に際しては、そのまま使用す
るか、または水等の希釈剤で所定濃度に希釈して使用す
ることができる。
When these preparations are actually used, they can be used as they are, or they can be diluted to a predetermined concentration with a diluent such as water.

ここにいう農薬補助剤としては、担体、乳化剤、懸濁剤
、分散剤、展着剤、浸透剤、湿潤剤、増粘剤、安定剤な
どが挙げられ、必要により適宜添加すればよい、担体と
しては、固体担体と液体担体に分けられ、固体担体とし
ては、澱粉、活性炭、大豆粉、小麦粉、木粉、魚粉、粉
乳などの動植物性粉末、タルク、カオリン、ベントナイ
ト、炭酸カルシウム、ゼオライト、珪藻土、ホワイトカ
ーボン、クレー、アルミナ、硫黄粉末などの鉱物性粉末
などが挙げられ、液体担体としては、水、メチルアルコ
ール、エチレングリコールなどのアルコール類、アセト
ン、メチルエチルケトンなどのケトン類、ジオキサン、
テイラヒドロフランなどのエーテル類、ケロシン、灯油
などの脂肪族炭化水素類、キシレン、トリメチルベンゼ
ン、テトラメチルベンゼン、シクロヘキサン、ソルベン
トナフサなどの芳香族炭化水素類、クロロホルム、クロ
ロベンゼンなどのハロゲン化炭化水素類、ジメチルホル
ムアミドなどの酸アミド類、酢酸エチルエステル、脂肪
酸のグリセリンエステルなどのエステル類、アセトニト
リルなどのニトリル類、ジメチルスルホキシドなどの含
硫化金物類などが挙げられる。
The agrochemical auxiliaries mentioned here include carriers, emulsifiers, suspending agents, dispersants, spreading agents, penetrating agents, wetting agents, thickeners, stabilizers, etc., and may be added as appropriate if necessary. They are divided into solid carriers and liquid carriers. Solid carriers include starch, activated carbon, soybean flour, wheat flour, wood flour, fish meal, animal and vegetable powders such as milk powder, talc, kaolin, bentonite, calcium carbonate, zeolite, and diatomaceous earth. Examples of liquid carriers include water, alcohols such as methyl alcohol and ethylene glycol, ketones such as acetone and methyl ethyl ketone, dioxane,
Ethers such as teirahydrofuran, aliphatic hydrocarbons such as kerosene and kerosene, aromatic hydrocarbons such as xylene, trimethylbenzene, tetramethylbenzene, cyclohexane, and solvent naphtha, and halogenated hydrocarbons such as chloroform and chlorobenzene. , acid amides such as dimethylformamide, esters such as ethyl acetate and glycerin ester of fatty acids, nitrites such as acetonitrile, and sulfide-containing metals such as dimethyl sulfoxide.

また、必要に応じて他の農薬、例えば殺虫剤、殺ダニ剤
、殺線虫剤、殺菌剤、抗ウィルス剤、誘引剤、除草剤、
植物成長調整剤などと混用、併用することができ、この
場合に一層優れた効果を示すこともある。
In addition, other agricultural chemicals such as insecticides, acaricides, nematicides, fungicides, antiviral agents, attractants, herbicides,
It can be mixed or used in combination with plant growth regulators, etc., and may exhibit even better effects in this case.

本発明の有害動物防除剤は一般に1〜20,0OOpp
麟望ましくは20〜2,000 ppmの有効成分濃度
で施用する。これらの有効成分濃度は、製剤の形態及び
施用する方法、目的、時期、場所及び害虫の発生状況等
によって適当に変更できる0例えば、水生有害虫の場合
、上記濃度範囲の薬液を発生場所に散布しても防除でき
るので、水中での有効成分濃度範囲は上記以下である。
The pest control agent of the present invention generally has a content of 1 to 20,0 OOpp.
It is preferably applied at an active ingredient concentration of 20 to 2,000 ppm. The concentration of these active ingredients can be changed appropriately depending on the form of the preparation, application method, purpose, timing, location, pest outbreak status, etc. For example, in the case of aquatic pests, a chemical solution with the above concentration range can be sprayed on the outbreak site. However, the concentration range of the active ingredient in water is below the above range.

単位面積あたりの施用量は10a当たり、有効成分化合
物として約0.1〜5.000g、好ましくは10〜1
 、000.が使用される。
The application amount per unit area is about 0.1 to 5.000 g, preferably 10 to 1 g, as the active ingredient compound per 10 a.
,000. is used.

しかし、特別の場合には、これらの範囲を逸脱すること
も可能である。また、−a式(I)で表わされる化合物
と他の特定の化合物との配合比率は、0.1〜100:
0゜005〜100、望ましくは、1〜50:0.01
〜50である。
However, in special cases it is also possible to depart from these ranges. Moreover, the compounding ratio of the compound represented by formula (I) and other specific compounds is 0.1 to 100:
0°005-100, preferably 1-50:0.01
~50.

本発明の化合物を含有する種々の製剤、またはその希釈
剤の施用は、通常一般に行われている施用方法すなわち
、散布(例えば散布、噴霧、ミスティング、アトマイジ
ング、散粒、水面施用等)、土壌施用(混入、潅注等)
、表面施用(塗布、粉衣、被覆等)、浸漬毒餌等により
行うことができる。またいわゆる超高濃度少量散布法(
ultralow volume)により施用すること
もできる。この方法おいては、活性成分を100%含有
することが可能である。
The various formulations containing the compounds of the present invention or their diluents can be applied by commonly used application methods, such as scattering (e.g., scattering, spraying, misting, atomizing, dusting, surface application, etc.); Soil application (mixing, irrigation, etc.)
It can be carried out by surface application (painting, powder coating, coating, etc.), immersion of poison bait, etc. Also, the so-called ultra-high concentration small amount spraying method (
It can also be applied at ultralow volumes. In this way, 100% active ingredient content is possible.

(実施例) 以下に本発明に係る試験例を記載する。(Example) Test examples according to the present invention will be described below.

試験例1゜ 1/3000アールポツトに畑土壌を詰め、後記製剤例
に準じて製剤した有効成分化合物製剤品の所定量を散布
処理し、表層下5cmまでの土壌と均一に混和した。そ
こへタマネギ苗を移植し、移植後2日目にタマネギバエ
2令幼虫をポットあたりlO頭放虫した。放虫後14日
目にタマネギ苗の被害株数を調査し、下記式により防除
価を求め、その結果を第6−1表及び第6−2表に示す
Test Example 1 Field soil was filled in a 1/3000-acre pot, and a predetermined amount of the active ingredient compound formulation prepared according to the formulation example described later was sprayed and mixed uniformly with the soil up to 5 cm below the surface layer. Onion seedlings were transplanted there, and on the second day after transplantation, 10 onion fly 2nd instar larvae were released per pot. The number of damaged onion seedlings was investigated on the 14th day after the insect release, and the control value was calculated using the following formula, and the results are shown in Tables 6-1 and 6-2.

防除価(%)− 第6表−1(粒剤処理) 第6表−2(粒剤処理) 前記試験例に於て、化合物A−5に対し化合物B−1、
B−2又はB−4をそれぞれ有効成分当り100及び2
00 g / 10 aで粒剤処理することにより各試
験区で100%の防除価が得られた。
Control value (%) - Table 6-1 (granule treatment) Table 6-2 (granule treatment) In the above test example, compound B-1,
100 and 2 of B-2 or B-4 per active ingredient, respectively.
By treating with granules at 00 g/10 a, 100% control value was obtained in each test plot.

また、化合物A−5に対し化合物C−4をそれぞれ10
0及び200g/10aで粉剤処理することによっても
それぞれ100%の防除価が得られた。
In addition, 10% of compound C-4 was added to compound A-5, respectively.
Powder treatment with 0 and 200 g/10a also gave a control value of 100%, respectively.

試験例2 1/3000 aポア)に畑土壌を詰め、後記製剤例に
準じて製剤した有効成分化合物製剤品の所定量を散布処
理し、表層下5cmまでの土壌と均一に混和した。そこ
へキュウリを播種し、播種後7日目にウリハムシ2令幼
虫をポットあたり10頭放虫した。放出後15日目に発
芽したキュウリ苗の被害株数を調査し、前記試験例1と
同様の方法で防除価を求め、その結果を第7表に示す。
Test Example 2 A 1/3000 a pore) was filled with field soil, and a predetermined amount of the active ingredient compound formulation prepared according to the formulation example described later was sprayed and mixed uniformly with the soil up to 5 cm below the surface layer. Cucumbers were sown there, and on the 7th day after sowing, 10 second instar cucurbit beetle larvae were released per pot. The number of damaged cucumber seedlings that germinated on the 15th day after release was investigated, and the control value was determined in the same manner as in Test Example 1. The results are shown in Table 7.

第7表 (粒剤処理) 前記試験例に於て、化合物A−5に対し化合物B−1を
有効成分当りそれぞれ50g/10aで粒剤処理するこ
とにより或いは化合物A−5に対し化合物B−7又はB
−8を有効成分当りそれぞれ50g/10aで粉剤処理
することにより、各試験区で100%の防除価が得られ
た。
Table 7 (Granule treatment) In the above test example, Compound A-5 was treated with Compound B-1 at 50 g/10a per active ingredient, or Compound A-5 was treated with Compound B-1. 7 or B
-8 was treated with powder at 50g/10a per active ingredient, and a control value of 100% was obtained in each test plot.

試験例3 後記製剤例に準じて製剤された有効成分化合物の製剤品
を水に分散させ、所定の濃度に調整した。
Test Example 3 A formulation of the active ingredient compound prepared according to the formulation example described below was dispersed in water and adjusted to a predetermined concentration.

ナスを植えた圃場を1区1.5rrr(I区につき6株
)に区切り、ナスに種々の生育ステージのナミハダニを
接種し、生育させた。前記所定濃度の薬液を10アール
当り300iになるようにナスの茎葉部に散布処理した
。散布直前、散布後7日目及び散布後144日目6株の
2葉(I区当り12葉)に寄生するナミハダニの成虫数
を調査した。
The field where eggplants were planted was divided into 1.5 rrr per plot (6 plants per plot), and the eggplants were inoculated with two-spotted spider mites at various growth stages and allowed to grow. The chemical solution having the predetermined concentration was sprayed onto the stems and leaves of the eggplant at a rate of 300 i/10 are. Immediately before spraying, 7 days after spraying, and 144 days after spraying, the number of adult two-spotted spider mites parasitic on two leaves of six plants (12 leaves per section I) was investigated.

その結果を第8表に示す。The results are shown in Table 8.

−第1表 試験例4 サツマイモを寄生として増殖させたサツマイモネコブセ
ンチュウで汚染された圃場を1区1.2−に区切り、後
記製剤例に準じて製剤された有効成分化合物製剤品の所
定量を作条に施用し、表層下5cmまでの土壌と均一に
混和した。
- Table 1 Test Example 4 A field contaminated with sweet potato knot nematodes grown as parasitic sweet potatoes was divided into 1 section, 1.2 sections, and a predetermined amount of the active ingredient compound formulation prepared according to the formulation example below was prepared. It was applied to the rows and mixed uniformly with the soil up to 5 cm below the surface layer.

そこに4〜5葉期のトマト苗を定植し、カブラヤガ3令
幼虫を定植後4日目及び7日目にそれぞれ15頭づつ、
並びに9日目に10頭を各処理区の土壌中に放った。
Tomato seedlings at the 4- to 5-leaf stage were planted there, and 15 Kabra Yaga 3rd instar larvae were planted on the 4th and 7th day after planting.
On the 9th day, 10 animals were released into the soil of each treatment area.

カブラヤガの防除価及びサツマイモネコブセンチェウの
着生程度を下記の方法によって求め、その結果を第9表
に示す。
The control value of Kabra Yaga moth and the degree of settlement of Sweet Potato Cucumber was determined by the following method, and the results are shown in Table 9.

(i)カブラヤガの防除価 トマト苗定植後18日目に被害程度を調査し、下記式に
より防除価を求めた。
(i) Control value of Kabra Yaga moth The degree of damage was investigated on the 18th day after planting tomato seedlings, and the control value was calculated using the following formula.

(ii )サツマイモネコブセンチュウの着生程度トマ
ト苗定植後30日目に根部を抜き取り、下記基準により
ネコブセンチュウの着生程度を求めた。
(ii) Degree of epiphytization of sweet potato nematode The roots of tomato seedlings were extracted on the 30th day after planting, and the degree of establishment of nematode nematode on sweet potato was determined according to the following criteria.

ネコブセンチュウの着生程度 〇−着生なし 5=50%着生 10−100%着生 第9表 また、前記試験例に於て、化合物1kA−5の代わりに
、例えば化合物NIA−4、A−7a、A−7b、、A
−20、A−21、A−25、A−32又はA−33を
用いても同様の結果が得られる。
Degree of settlement of Nematode 0 - No settlement 5 = 50% settlement 10 - 100% settlement 7a, A-7b,,A
Similar results can be obtained using -20, A-21, A-25, A-32 or A-33.

製剤例1 +11  クレーの無成分造粒品(商品名:アプルスN
1イソライト工業91製’)      91.8重量
部(2)化合物阻A−55〃 (3)化合物患D−10,2〃 (4)  ポリオキシエチレンアルキルアリールエーテ
ル           l   #(5)トリメチル
ベンゼン      2  #上記(2)〜(5)を混
合したものを、+l+に吹き付は粒剤とした。
Formulation example 1 +11 Ingredient-free granulated clay product (product name: Apulus N
1 Isolite Kogyo 91) 91.8 parts by weight (2) Compound A-55 (3) Compound D-10,2 (4) Polyoxyethylene alkylaryl ether 1 # (5) Trimethylbenzene 2 # A mixture of the above (2) to (5) was sprayed onto +l+ to form granules.

製剤例2 (I)  クレーの無成分造粒品(製剤例1(I)と同
様)91  重量部 (2)化合物隘A−52,5〃 (3)化合物隘C−12,5〃 (4)ポリオキシエチレンアルキルアリールエーテル 
          2  #(5)トリメチルベンゼ
ン      2  〃上記(2)〜(5)を混合した
ものを、(I1に吹き付は粒剤とした。
Formulation Example 2 (I) Ingredient-free granulated clay (same as Formulation Example 1 (I)) 91 parts by weight (2) Compound A-52,5 (3) Compound C-12,5 (4 ) Polyoxyethylene alkylaryl ether
2 #(5) Trimethylbenzene 2 A mixture of the above (2) to (5) was sprayed onto I1 to form granules.

製剤例3 fl+  クレーの無成分造粒品(製剤例1(工)と同
様)90 ffl量部 (2)化合物隘A−53〃 (3)化合動磁11−1          3  〃
(4)  ポリオキシエチレンアルキルアリールエーテ
ル            2 #(5)トリメチルベ
ンゼン       2 〃上記(2)〜(5)を混合
したものを、fl)に吹き付は粒剤とした。
Formulation example 3 fl+ Clay non-component granulated product (same as Formulation example 1 (technical)) 90 parts ffl (2) Compound A-53 (3) Compound magnetic dynamic 11-1 3
(4) Polyoxyethylene alkylaryl ether 2 #(5) Trimethylbenzene 2 A mixture of the above (2) to (5) was sprayed onto fl) to form granules.

製剤例4 +11  粉末クレー         97.5重量
部(2)  低級アルコールリン酸エステル 0.5〃
(3)  化合物阻A−51,0− (4)化合物11hB−71,0〃 以上の成分を均一に混合して、粉剤とした。
Formulation Example 4 +11 Powdered clay 97.5 parts by weight (2) Lower alcohol phosphate ester 0.5
(3) Compound A-51,0- (4) Compound 11hB-71,0 The above components were uniformly mixed to form a powder.

製剤例5 +l+  化合動磁^−515重量部 (2)化合物11hB−1015〃 (3)  アセトニトリル        30#(4
)  キシレン           27〃(5) 
 ポリオキシエチレンスチリルフェニルエーテル   
         10〃(6)  アルキルアリール
スルホネート  3 〃以上の成分を均一に混合して乳
剤とした。
Formulation Example 5 +l+ Compound Magnetism^-515 parts by weight (2) Compound 11hB-1015〃 (3) Acetonitrile 30# (4
) Xylene 27〃(5)
Polyoxyethylene styryl phenyl ether
10 (6) Alkylaryl sulfonate 3 The above components were uniformly mixed to form an emulsion.

以上that's all

Claims (1)

【特許請求の範囲】  一般式( I ) ▲数式、化学式、表等があります▼・・・( I ) (式中、X_1及びX_3は、水素原子;ハロゲン原子
、アルコキシ基、アルキルチオ基、フェノキシ基、ハロ
ゲン置換フェノキシ基、フェニルチオ基もしくはハロゲ
ン置換フェニルチオ基で置換されてもよいアルキル基或
いはアルコキシ基;カルボキシル基;アルコキシカルボ
ニル基;又はハロゲン原子で置換されてもよいフェニル
基であり、X_2及びX_4は水素原子又はアルキル基
であり、X_2及びX_3は一緒になりアルキレン基を
形成してもよく、Y_1、Y_2及びZは酸素原子又は
硫黄原子であり、R_1及びR_2はアルキル基である
)で表わされる化合物と有機リン系化合物、カーバメー
ト系化合物、ピレスロイド系化合物、ウレア系化合物、
スルフォン系化合物又はN−ピリジルアニリン系化合物
の少なくとも一種とを有効成分として含有することを特
徴とする有害動物防除剤。
[Claims] General formula (I) ▲Mathematical formula, chemical formula, table, etc.▼... (I) (In the formula, X_1 and X_3 are hydrogen atoms; halogen atom, alkoxy group, alkylthio group, phenoxy group , a halogen-substituted phenoxy group, a phenylthio group, or an alkyl group or alkoxy group that may be substituted with a halogen-substituted phenylthio group; a carboxyl group; an alkoxycarbonyl group; or a phenyl group that may be substituted with a halogen atom, and X_2 and X_4 are is a hydrogen atom or an alkyl group, X_2 and X_3 may be taken together to form an alkylene group, Y_1, Y_2 and Z are an oxygen atom or a sulfur atom, and R_1 and R_2 are an alkyl group) Compounds and organic phosphorus compounds, carbamate compounds, pyrethroid compounds, urea compounds,
A pest control agent comprising at least one of a sulfone compound or an N-pyridylaniline compound as an active ingredient.
JP63065050A 1988-03-18 1988-03-18 Control agent of harmful animal Pending JPH01238505A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63065050A JPH01238505A (en) 1988-03-18 1988-03-18 Control agent of harmful animal

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63065050A JPH01238505A (en) 1988-03-18 1988-03-18 Control agent of harmful animal

Publications (1)

Publication Number Publication Date
JPH01238505A true JPH01238505A (en) 1989-09-22

Family

ID=13275745

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63065050A Pending JPH01238505A (en) 1988-03-18 1988-03-18 Control agent of harmful animal

Country Status (1)

Country Link
JP (1) JPH01238505A (en)

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Publication number Priority date Publication date Assignee Title
ES2102965A1 (en) * 1994-12-23 1997-08-01 Agrides S A Multi-purpose broad-spectrum insecticidal product.
WO2005070206A1 (en) * 2004-01-23 2005-08-04 Ishihara Sangyo Kaisha, Ltd. Pest control composition and method of controlling pest
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CN102246818A (en) * 2011-08-08 2011-11-23 陕西美邦农药有限公司 Insecticidal composition containing organophosphorus compound
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