JPH03261704A - Granule for pest control - Google Patents

Granule for pest control

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Publication number
JPH03261704A
JPH03261704A JP2060582A JP6058290A JPH03261704A JP H03261704 A JPH03261704 A JP H03261704A JP 2060582 A JP2060582 A JP 2060582A JP 6058290 A JP6058290 A JP 6058290A JP H03261704 A JPH03261704 A JP H03261704A
Authority
JP
Japan
Prior art keywords
granules
compound
granule
active ingredient
parts
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
JP2060582A
Other languages
Japanese (ja)
Inventor
Koichi Suzuki
宏一 鈴木
Toshiyuki Umehara
利之 梅原
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 JP2060582A priority Critical patent/JPH03261704A/en
Publication of JPH03261704A publication Critical patent/JPH03261704A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To provide the title granules containing, as active ingredient, an insecticide/herbicide consisting of 1-(6-chloro-3-pyridylmethyl)-N- nitroimidazolidin-2-ylideneamine and sulfoniumurea-based compound (s). CONSTITUTION:The objective granules containing, as active ingredient, (A) 1-(6-chloro-3-pyridylmethyl)-N-nitroimidazolidin-2-ylideneamine and (B) at least one sulfonylurea-based compound {esp.pref. ethyl-5-[3-(4,6-dimethoxypyrimidin-2- yl)-ureidosulfonyl]-1-methylpyrazole-4-carboxylate}. The present active ingredient is further incorporated with one or more herbicidal active ingredients for Allium macrostemon, etc., into a granular agent for paddy. The present granules is such an agent as to enable weed control over a long period of time in a single application.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、特定の公知の殺虫剤活性成分と特定の公知の
除草剤活性成分とを有効成分として含有する新規な有害
生物防除用粒剤に関するもので特に水田用粒剤に関する
ものである。
[Detailed Description of the Invention] [Industrial Application Field] The present invention provides a novel pest control granule containing a specific known insecticide active ingredient and a specific known herbicide active ingredient as active ingredients. In particular, it relates to granules for use in paddy fields.

〔従来の技術および課題〕[Conventional technology and issues]

従来、水田用の粒剤に関しては除草粒剤、特に2種以上
の除草活性成分を含有する粒剤はよく知られ、用いられ
ている。
Conventionally, herbicidal granules, especially granules containing two or more types of herbicidal active ingredients, have been well known and used as granules for paddy fields.

また、水田用の殺虫粒剤についても知られているが、殺
虫活性成分と除草活性成分とを同時にひとつの粒剤に含
有された水田用粒剤は、あまり知られていない。
Insecticidal granules for paddy fields are also known, but granules for paddy fields that contain both an insecticidal active ingredient and a herbicidal active ingredient in one granule are not well known.

近年、水稲の分野においては、省力化および低コスト化
が望まれ、1回の農薬粒剤の散布で主要な水稲害虫を防
除するとともに同時に水田雑草を長期間に渡って防除す
ることが可能な水田用の粒剤の出現が要望されている。
In recent years, in the field of paddy rice, labor saving and cost reduction have been desired, and it is now possible to control major paddy rice pests and at the same time control paddy field weeds over a long period of time by spraying pesticide granules once. There is a demand for the appearance of granules for paddy fields.

〔課題を解決するための手段〕[Means to solve the problem]

本発明は、 (1)I−(6−クロロ−3−ピリジルメチル)N−ニ
ドロイくダシリジン−2−イリデンアミン〔以下、化合
物(1)という〕と、スルボニルウレア系化合物の1種
以上とを有効成分として含有する有害生物防除用粒剤6 (2)上記の第1項記載の有効成分と、ノビエ等に有効
な除草剤活性成分のI種以上とを有効成分として含有す
る水田用粒剤。
The present invention comprises (1) I-(6-chloro-3-pyridylmethyl)N-nidroidecilidin-2-ylideneamine [hereinafter referred to as compound (1)] and one or more sulbonyl urea compounds as active ingredients. (2) A granule for use in paddy fields containing as active ingredients the active ingredient described in item 1 above and one or more types I or more of herbicide active ingredients effective against grasshoppers and the like.

(3)スルホニルウレア系化合物が、下記の4種の化合
物のいずれかである上記の第1項記載の有害生物防除用
粒剤。
(3) The granules for controlling pests according to item 1 above, wherein the sulfonylurea compound is any of the following four types of compounds.

■ エチル−5−[3−(4,6−ジメトキシピリミジ
ン−2−イル)−ウレイドスルホニル)−1−メチルピ
ラゾール−4−カルボキシレート〔以下、化合物(2)
という〕、■ メチル=α(4,6−シメトキシビリミ
ジンー2−イルカルバモイルスルファモイル)−〇−ト
ルアート〔以下、化合物(3)という)、 ■ 3−(4,6−ジメトキシ−1,3.5−トリアジ
ン−2−イル)−1−(2−(2−メトキシエトキシ)
−フェニルスルボニルツウレア〔以下、化合物(4)と
いう〕、■ N−(2−クロロイミダゾ−(1,2−a
]ピリミジン3−イルスルホニル)−N’(4,6−ジ
メトキシ−2−ピリミジニル)ウレア〔以下、化合物(
5)という]。
■ Ethyl-5-[3-(4,6-dimethoxypyrimidin-2-yl)-ureidosulfonyl)-1-methylpyrazole-4-carboxylate [hereinafter referred to as compound (2)]
], ■ Methyl = α(4,6-cymethoxypyrimidin-2-ylcarbamoylsulfamoyl)-〇-toluate [hereinafter referred to as compound (3)], ■ 3-(4,6-dimethoxy-1) ,3.5-triazin-2-yl)-1-(2-(2-methoxyethoxy)
-Phenylsulfonyltourea [hereinafter referred to as compound (4)], ■ N-(2-chloroimidazo-(1,2-a
]pyrimidin-3-ylsulfonyl)-N'(4,6-dimethoxy-2-pyrimidinyl)urea [hereinafter referred to as compound (
5)].

に関するものである。It is related to.

本発明において、化合物(1)は特開昭61−2675
75号公報に記載された公知殺虫剤であり粒剤の形で、
水稲の移植後に水中へ施用しても長時間の効力の持続が
期待出来る。
In the present invention, compound (1) is
A known insecticide described in Publication No. 75, in the form of granules,
Even when applied underwater after transplanting paddy rice, it can be expected to maintain its efficacy for a long time.

一方、化合物(2)〜(5)で示される化合物は、公知
のスルホニルウレア系化合物であり、非常に低薬量の水
稲用除草剤で、単用で用いるか、またはノビエ等に有効
な化合物との混合で用いることによって、1回の処理で
長期間の雑草防除が可能な薬剤である。
On the other hand, the compounds represented by compounds (2) to (5) are known sulfonylurea compounds, and are very low-dose herbicides for paddy rice, and can be used alone or as compounds effective against grasshoppers, etc. By using a mixture of these agents, it is possible to control weeds for a long period of time with a single treatment.

本発明者等は、化合物(1)と、化合物(2)〜(5)
で示されるスルホニルウレア系化合物との混合粒剤を用
いるか、またはこれらの化合物にさらにノビエ等に有効
な化合物とを含む混合粒剤を用いることによって、1回
の農薬粒剤の散布で主要な水稲害虫を防除するととも番
こ同時に水田雑草を長期間に渡って防除することが可能
な事を見出し、本発明を完成させた。
The present inventors have developed compound (1) and compounds (2) to (5).
By using a mixed granule with a sulfonylurea compound represented by the formula, or a mixed granule containing these compounds and a compound effective against grasshoppers, major paddy rice plants can be killed with a single application of pesticide granules. The present invention was completed by discovering that it is possible to control pests and paddy field weeds for a long period of time at the same time as pest control.

本発明において、化合物(2)の−船名はピラゾスルフ
ロンエチルで、化1f(3)の−船名ハヘンスルフロン
メチルで、化合物(4)の−船名はジノスルフロンで、
化合物(5)の試験名はTH−913である。
In the present invention, the ship name of compound (2) is pyrazosulfuron ethyl, the ship name of compound (3) is hahensulfuron methyl, and the ship name of compound (4) is dinosulfuron,
The test name of compound (5) is TH-913.

また、ノビエ等に有効な薬剤としては、例えば、ビラプ
レート(−船名)、ビラジキシフェン(−船名)、ペン
ゾフェナップ(−船名)、ダイムロン〔−船名)、ブロ
モブチド(−船名)、ナブロアニリド(−船名)、クロ
メプロップ(−船名)(試験名はMY−15)、GNP
 (−船名)、クロメトキシニル(−船名)、ビフェノ
ックス(−船名)、オキサシアシン(−船名)、メフェ
ナセット(−船名)、ブタクロール(−船名)、プレチ
ラクロール(−船名)、ブタクロール(−船名)(試験
名はKH−218) 、ジチオピル(−船名)(試験名
はMON−72) 、ペンフレセード(−船名)(試験
名はNS−112)、ピリブチカルブ(−船名)(試験
名はTSH−888)、ベンチオカーブ(−船名)、ジ
メピペレート(−船名)、ニスプロカルブ(−Ml <
 −E−!J ネート(−船名)、プタミホス(−船名
)、キンクロラック(−船名)、シンメスリン(−船名
)、シメトリン(−船名)、5AP(−船名)、ジメタ
メトリン(−船名)、2’   3’ −ジクロロ−4
−エトキシメトキシベンズアリニド(試験名はHW−5
2>、1−(2−クロロベンジル)−3−(α、α−ジ
メチルベンジル)尿素(試験名はJC−940)、N−
[2” −(3゛−メトキシ)−チエニルメチルゴーN
−クロロアセト−2゜6−シメチルアニリド(試験名は
N5K−850)等が挙げられる。
In addition, effective drugs for noviet, etc. include, for example, Viraplate (-ship name), Viradixifene (-ship name), Penzofenap (-ship name), Daimron [-ship name), Bromobutide (-ship name), Nabroanilide. (-ship name), Kuromeprop (-ship name) (test name is MY-15), GNP
(-ship name), clomethoxynil (-ship name), bifenox (-ship name), oxacyacin (-ship name), mefenacet (-ship name), butachlor (-ship name), pretilachlor (-ship name), butachlor ( - ship name) (test name is KH-218), dithiopyr (- ship name) (test name is MON-72), penfresade (- ship name) (test name is NS-112), pyributicarb (- ship name) ( The test names are TSH-888), bentiocarb (-ship name), dimepiperate (-ship name), nisprocarb (-Ml <
-E-! J Nate (-ship name), ptamiphos (-ship name), quinclorac (-ship name), synmethrine (-ship name), cymetrine (-ship name), 5AP (-ship name), dimethamethrine (-ship name) , 2'3' -dichloro-4
-Ethoxymethoxybenzarinide (test name is HW-5
2>, 1-(2-chlorobenzyl)-3-(α,α-dimethylbenzyl)urea (test name is JC-940), N-
[2”-(3′-methoxy)-thienylmethylgoN
-Chloroaceto-2°6-dimethylanilide (test name: N5K-850) and the like.

本発明における化合物(1)と化合物(2)〜(5)の
化合物の使用割合は、各々の剤の性能を実質的に損なわ
ない範囲で適宜選択することが出来る。
The ratio of compound (1) and compounds (2) to (5) in the present invention can be appropriately selected within a range that does not substantially impair the performance of each agent.

例えば、化合物(2)〜(5)が、1重量部に対し、化
合物(1)が、1〜100重量部の範囲で、より望まし
くは3〜30重量部の範囲の使用割合がよい。
For example, the ratio of compound (1) to 1 part by weight of compounds (2) to (5) is 1 to 100 parts by weight, more preferably 3 to 30 parts by weight.

上記のこれらの化合物にさらにノビエ等に有効である上
記化合物を適宜混合することが出来る。
In addition to the above-mentioned compounds, the above-mentioned compounds that are effective against noviae and the like can be appropriately mixed.

上記の活性成分化合物を含む本発明の有害生物防除用粒
剤を作るために、各種の助剤類を更に含有することがで
き、公知の手法に従って製剤することが出来る。
In order to prepare the pest control granules of the present invention containing the above-mentioned active ingredient compounds, various auxiliary agents can be further included, and the preparations can be carried out according to known methods.

助剤類としては、例えば固体担体、界面活性剤などが挙
げられる。
Examples of the auxiliary agents include solid carriers and surfactants.

固体担体としては具体的に、カオリナイト、モンモリロ
ナイト、珪藻土、ベントナイト、タルク、クレー、炭酸
カルシウム、硫酸カルシウム、硫酸アンモニウム等が挙
げられ、界面活性剤体としては具体的に、アルキルベン
ゼンスルホン酸塩、ポリオキシエチレンアルキルアリル
エーテル、リグニンスルホン酸塩、アルキルスルホコハ
ク酸塩、ポリオキシエチレン脂肪酸エステル−、ナフタ
レンスルホン酸塩、ポリオキシエチレンアルキルアリル
エーテル硫酸塩、アルキルアミン塩、トリポリリン酸塩
などが挙げられる。
Specific examples of the solid carrier include kaolinite, montmorillonite, diatomaceous earth, bentonite, talc, clay, calcium carbonate, calcium sulfate, ammonium sulfate, etc., and specific examples of the surfactant include alkylbenzene sulfonate, polyoxy Examples include ethylene alkyl allyl ether, lignin sulfonate, alkyl sulfosuccinate, polyoxyethylene fatty acid ester, naphthalene sulfonate, polyoxyethylene alkyl allyl ether sulfate, alkyl amine salt, and tripolyphosphate.

これら界面活性剤の含有量は、特に塵定されるものでは
ないが、本発明の粒剤100重量部に対し、通常0.0
5〜20重量部の範囲が望ましい。
The content of these surfactants is not particularly determined, but is usually 0.0 parts by weight per 100 parts by weight of the granules of the present invention.
A range of 5 to 20 parts by weight is desirable.

また、必要に応して、エポキシ化大豆油等の分解防止剤
を本発明の粒剤に含有させてもよい。
Furthermore, if necessary, the granules of the present invention may contain a decomposition inhibitor such as epoxidized soybean oil.

次に、本発明の粒剤の配合実施例を具体的に記載するが
、本発明はこれらのみに限定されるものではない。
Next, formulation examples of the granules of the present invention will be specifically described, but the present invention is not limited thereto.

なお、以下の部は、重量部を意味する。In addition, the following parts mean parts by weight.

(以下、余白) R1」」動糺上 化合物(1)             1  部化合
物(2)              0.07部DB
SN      3部 エポキシ化大豆油 −−−一−・−−−−−−−−−−
一・−−−1部ベントナイト   −−−−−−−・・
−−−−−−−−−30部タルク       −・−
−−−〜−−−−−・−−−−64,93部以上を均一
に混合粉砕して、少量の水を加え撹拌し、押出造粒機で
造粒し、造粒後乾燥して粒剤を得た。
(Hereinafter, blank space) R1'' Compound (1) 1 part Compound (2) 0.07 part DB
SN 3-part epoxidized soybean oil ---1-・--------
1・---1 part bentonite -----------・
−−−−−−−−30 parts talc −・−
−−−〜−−−−−・−−−−64.93 parts or more are uniformly mixed and pulverized, a small amount of water is added and stirred, granulated with an extrusion granulator, and dried after granulation. Granules were obtained.

なお、上記のDBSNは、ドデシルベンゼンスルホン酸
ナトリウムを意味するもので、以下の配合実施例におい
ても同じである。
Note that the above DBSN means sodium dodecylbenzenesulfonate, and the same applies to the following formulation examples.

(以下、余白) 配治1a動組i 化合物(1)    −・・−−−−−・−−−−−一
−−−・・−1部化合物(2)    ・   −・−
一一一一一〜   0.07部メフェナセット  −・
−・−一−−−−・−・・−−−一−−・−3,5部D
BSN  −・・・−・−・・・−・・−3部エポキシ
化大豆油 −・−・−・−・・・−・・−・−・−・−
工  部ベントナイト   −・・−−−−一−・・−
・・−・・−30部タルク      −・−・・・−
・・−・・・−−−−−61,43部以上を均一に混合
粉砕して、少量の水を加え攪拌し、押出造粒機で造粒し
、造粒後乾燥して粒剤を得た。
(Hereafter, blank space) Kaiji 1a Motion i Compound (1) −・・−−−−−・−−−−−1−−−・・−1 part compound (2) ・ −・−
11111 ~ 0.07 part mefena set -・
−・−1−−−−・−・・−−−1−−・−3,5 part D
BSN −・−・−・・−・−3 parts epoxidized soybean oil −・−・−・−・−・・・−・−・−・−
Engineering department bentonite −・・−−−−1−・・−
・・−・・−30 parts talc −・−・・−
・・・・・−−−−−−61.43 parts or more are mixed and pulverized uniformly, a small amount of water is added and stirred, granulated with an extrusion granulator, and after granulation, dried to form granules. Obtained.

L金1豊囲主 化合物(1)    ・−−一一−−−−−−−−・−
・−・−・−1部化合物(,2)     −−−−−
−−−−−−−−−・・・−・−0,07部キンクロラ
ック  ・−・−・・−−−一−−−−−・−−−−−
一・−0,9部プレチラクロール −・・−・−・−・
−−−−−−−−−1、5部DBSN  −・・−・−
・−・−・−・−・ 3部エポキシ化大豆油 ・−=−
・・−・−−−−−−−一−・   1  部ベントナ
イト   ・・−−−一−−−−・−−−−−−−−−
−・−30部タルク      ・−−−−−−−m−
・−−−−−−−−−−−−−62,53部以上を均一
に混合粉砕して、少量の水を加え攪拌し、押出造粒機で
造粒し、造粒後乾燥して粒剤を得た。
L gold 1 rich main compound (1) ・−−11−−−−−−−・−
・−・−・−1 part compound (,2) −−−−−
−−−−−−−−−・・・−・−0,07 parts Quinclorac ・−・−・・−−−1−−−−−・−−−−
1・-0,9 parts pretilachlor −・・−・−・−・
−−−−−−−−1, 5th copy DBSN −・・−・−
・−・−・−・−・ 3-part epoxidized soybean oil ・−=−
・・−・−−−−−−−1−・ 1 part bentonite ・・−−−1−−−−・−−−−−−−−
−・−30 parts talc ・−−−−−−m−
・------------------ Mix and pulverize 62,53 parts or more uniformly, add a small amount of water and stir, granulate with an extrusion granulator, and dry after granulating. Granules were obtained.

L全1見員工 化合物(1)    −・−−一−−−−−−−−・−
−−−−−−1部化合物(3)     −−−−−−
−−−−−−・−・−・−0,17部メフェナセット 
 ・−−−−−・−−−−−−−−−−−−3,5部ダ
イムロン    −−−−−−−−・−−−−−−−−
−−−−1、5部DB SN  、−−−−・・−−−
−−−−−−−−−−−−−3部エポキシ化大豆油 −
・−−−−−−−−−−−−−−1部ベントナイト  
 −・−−−−一−−・−−−−m−・−−−30部タ
ルク      −・−−−−−・−・−・−、−59
,83部以上を均一に混合粉砕して、少量の水を加え攪
拌し、押出造粒機で造粒し、造粒後乾燥して粒剤を得た
L total 1 compound (1) −・−−1−−−−−−−−・−
-------- Part 1 compound (3) -------
−−−−−−・−・−・−0.17 part mefena set
・−−−−−−−−−−−−−−−−−−3,5 part Daimron −−−−−−−−・−−−−−−−−
-----1, 5th copy DB SN, -----・・---
−−−−−−−−−−−−3-part epoxidized soybean oil −
・−−−−−−−−−−−−−−1 part bentonite
−・−−−−1−−・−−−−m−・−−30 parts talc −・−−−−−・−・−・−, −59
, 83 parts or more were uniformly mixed and pulverized, a small amount of water was added and stirred, granulated using an extrusion granulator, and after granulation, the mixture was dried to obtain granules.

(以下、余白) 配ffi動糺i 化合物(1)             1  部化合
物(4)              0.15部キン
クロラック   −・−一一−−−−−−−−・−−−
−−−−−・   0.7  部プレチラクロール −
−−−−−−−−−・−一−−−−−−1部DBSN 
 −−−−−−−−−−−−−−−−−−−−−−−3
部エポキシ化大豆油 −・−・・−・−・−・−−−−
−−−1部ベントナイト   −−−−−−−−−−−
−−−−・−・・−30部タルク       −−−
−−−−−・−・−・−・−・・・・−63゜15部以
上を均一に混合粉砕して、少量の水を加え撹拌し、押出
造粒機で造粒し、造粒後乾燥して粒剤を得た。
(Hereinafter, blank space) Compound (1) 1 part Compound (4) 0.15 parts Quinclorac
−−−−−・0.7 part pretilachlor −
−−−−−−−−−・−1−−−−−−1 part DBSN
−−−−−−−−−−−−−−−−−−−−3
Partially epoxidized soybean oil −・−・・−・−・−・−−−−
−−−1 part bentonite −−−−−−−−−−−
−−−−・−・・−30 parts talc −−−
−−−−−・−・−・−・−・・・・・63゜Mix or more of 15 parts uniformly, mix and pulverize, add a small amount of water and stir, granulate with an extrusion granulator, and granulate. After drying, granules were obtained.

(以下、余白) 配ffi鮎糺i 化合物(1)             1  部化合
物(5)              0.3  部キ
ンクロランク            1  部ダイム
ロン             5  部DBSN  
   3部 エポキシ化大豆油−−−−−−−−−−−−−−−−−
1部ベントナイト    −−−−−−−−−−−−−
−−−−30部タルク       −−−−−−・−
・−・・−・・−・−−−−−−−58,7部以上を均
一に混合粉砕して、少量の水を加え撹拌し、押出造ね機
で造粒し、造粒後乾燥して粒剤を得た。
(Hereinafter, blank space) Compound (1) 1 part Compound (5) 0.3 part Kincrorank 1 part Daimron 5 parts DBSN
3-part epoxidized soybean oil
1 part bentonite −−−−−−−−−−−−−
−−−−30 parts talc −−−−−−・−
・−・・−・・−・−−−−−−−58.7 parts or more are uniformly mixed and pulverized, a small amount of water is added and stirred, granulated with an extrusion machine, and dried after granulation. Granules were obtained.

次に、配合実施例1ないし配合実施例6で得た本発明の
粒剤を用いて、殺虫効果試験および除草効果試験をおこ
なった。
Next, using the granules of the present invention obtained in Formulation Example 1 to Formulation Example 6, an insecticidal effect test and a herbicidal effect test were conducted.

(以下、余白) 試l繁引り 育苗箱にて育成した稚苗(2,5葉、品種二日本晴)を
移植機にて切出し、その稚苗を、水田土壌を充填し代掻
きを行った1 /10.000アールのポットに移植し
た。
(Hereinafter, blank space) Young seedlings (2.5 leaves, cultivar Nihonbare) grown in a trial seedling box were cut out using a transplanter, and the young seedlings were filled with paddy soil and plowed. /10,000 are transplanted into a pot.

移植7日後に、配合実施例1〜6で作製した粒剤をアー
ル当り300gとなるよう水面施用した。
Seven days after transplantation, the granules prepared in Formulation Examples 1 to 6 were applied to the water surface in an amount of 300 g per area.

薬剤処理7日後、及び21日後にポットで生育中の稲に
ポリエチレン円筒を立て、有機リン剤及びカーバメート
剤に抵抗性のツマグロヨコバイ成虫及び、ヒメトビウン
カ成虫をポット当り10頭ずつ放ち、48時間後に死生
率を調査した。
Seven and 21 days after chemical treatment, polyethylene cylinders were erected on rice plants growing in pots, and 10 adult black leafhoppers and adult brown planthoppers, which are resistant to organic phosphorus agents and carbamate agents, were released into each pot, and the mortality rate was determined after 48 hours. investigated.

結果を第1表および第2表に示す。The results are shown in Tables 1 and 2.

(以下、余白) 第1表 ツマグロヨコバイの死生率 (%) 施用粒剤 300 g /7−ル 成虫48時間後の死生率(%) 処理7日後 処理21日後 配合実施例10粒剤 配合実施例2の粒剤 配合実施例3の粒剤 配合実施例4の粒剤 配合実施例5の粒剤 配合実施例6の粒剤 無処理区 第2表 ヒメ 00 00 00 00 00 00 00 00 00 00 00 00 トビウンカの死生率 (%) 施用粒剤 300 g /7−ル 配合実施例1の粒剤 配合実施例2の粒剤 配合実施例3の粒剤 配合実施例4の粒剤 配合実施例5の粒剤 配合実施例60粒剤 無処理区 成虫48時間後の死生率(%) 処理7日後 処理21日後 00 00  Oo  00 00 00 00 00 00 00 00 00 試m 115000  アールのワグネルボットに水田土壌を
詰め、代掻き後、ノビエ、ホタルイ、コナギ、キカシグ
サを播種し、ウリカワおよびミズガヤツリの塊茎を置床
した。
(Hereinafter, blank spaces) Table 1 Mortality rate of black leafhopper (%) Mortality rate after 48 hours of applied granules (300 g/7-l) 7 days after treatment 21 days after treatment Formulation Example 10 Granule Formulation Example 2 Granule formulation Example 3 Granule formulation Example 4 Granule formulation Example 5 Granule formulation Example 6 Granule untreated area Table 2 00 00 00 00 00 00 00 00 00 00 00 00 Mortality rate of flying planthopper (%) Application of granules 300 g/7-L Blend of Example 1 Granules Blend of Example 2 Granules Blend of Example 3 Granules Blend of Example 4 Granules Blend of Example 5 Granules Formulation Example 60 Mortality rate (%) of adults after 48 hours in granule-free area 7 days after treatment 21 days after treatment 00 00 Oo 00 00 00 00 00 00 00 00 00 Trial m 115000 Earl's Wagnerbot was filled with paddy soil , After plowing, we sowed wild grass, firefly, Japanese cypress, and Kikashigusa, and placed the tubers of Urikawa and Mizugaya cypress.

そして、試験例1と同様の水稲稚苗をポット当り2株定
植し、温室内で生育させた。
Then, two paddy rice seedlings similar to those in Test Example 1 were planted per pot and grown in a greenhouse.

移植7日後に配合実施例1〜6のね剤を1アール当り3
00gとなるように施用した。
7 days after transplantation, apply 3 of the formulation examples 1 to 6 per 1 are.
It was applied in an amount of 0.00 g.

処理後28日目に下記の基準に従って各雑草及び水稲へ
の影響を評価した。
On the 28th day after treatment, the effects on each weed and paddy rice were evaluated according to the following criteria.

判定基準 5 : 完全枯死あるいは90%以上の抑制4 : 7
0〜90%の抑制 3 : 40〜70%の抑制 2 : 20〜40%の抑制 御 :  5〜20%の抑制 0 :  5%以下の抑制 抑制の程度は、肉眼による観察調査から求めた。
Judgment Criterion 5: Complete death or 90% or more suppression 4: 7
0-90% inhibition 3: 40-70% inhibition 2: 20-40% inhibition: 5-20% inhibition 0: 5% or less inhibition The degree of inhibition was determined from visual observation.

結果を第3表に示す。The results are shown in Table 3.

第3表 除草効果及び水稲への影響 配合実施例1の粒剤 配合実施例2の粒剤 配合実施例30粒剤 配合実施例4の粒剤 配合実施例5の粒剤 配合実施例6の粒剤 無処理区 0Table 3 Weeding effect and impact on paddy rice Granules of Formulation Example 1 Granules of Formulation Example 2 Formulation Example 30 Granules Granules of Formulation Example 4 Granules of Formulation Example 5 Granules of Formulation Example 6 Untreated area 0

Claims (3)

【特許請求の範囲】[Claims] (1)1−(6−クロロ−3−ピリジルメチル)−N−
ニトロイミダゾリジン−2−イリデンアミンと、スルホ
ニルウレア系化合物の1種以上とを有効成分として含有
する有害生物防除用粒剤。
(1) 1-(6-chloro-3-pyridylmethyl)-N-
A granule for pest control containing nitroimidazolidin-2-ylideneamine and one or more sulfonylurea compounds as active ingredients.
(2)請求項第1項記載の有効成分と、ノビエ等に有効
な除草剤活性成分の1種以上とを有効成分として含有す
る水田用粒剤。
(2) A granule for paddy fields containing the active ingredient according to claim 1 and one or more types of herbicide active ingredients effective against grasshoppers, etc. as active ingredients.
(3)スルホニルウレア系化合物が、下記の4種の化合
物のいずれかである請求項第1項記載の有害生物防除用
粒剤。 [1]エチル−5−〔3−(4,6−ジメトキシピリミ
ジン−2−イル)−ウレイドスルホニル〕−1−メチル
ピラゾール−4−カルボキシレート、 [2]メチル=α(4,6−ジメトキシピリミジン−2
−イルカルバモイルスルファモイル)−0−トルアート
、 [3]3−(4,6−ジメトキシ−1,3,5−トリア
ジン−2−イル)−1−〔2−(2−メトキシエトキシ
)−フェニルスルホニル〕−ウレア、 [4]N−(2−クロロイミダゾ−〔1,2−a〕ピリ
ジン−3−イルスルホニル)−N′− (4,6−ジメトキシ−2−ピリミジニル)ウレア。
(3) The granules for controlling pests according to claim 1, wherein the sulfonylurea compound is any of the following four types of compounds. [1] Ethyl-5-[3-(4,6-dimethoxypyrimidin-2-yl)-ureidosulfonyl]-1-methylpyrazole-4-carboxylate, [2] Methyl α(4,6-dimethoxypyrimidine) -2
-ylcarbamoylsulfamoyl)-0-toluate, [3]3-(4,6-dimethoxy-1,3,5-triazin-2-yl)-1-[2-(2-methoxyethoxy)-phenyl [4]N-(2-chloroimidazo-[1,2-a]pyridin-3-ylsulfonyl)-N'-(4,6-dimethoxy-2-pyrimidinyl)urea.
JP2060582A 1990-03-12 1990-03-12 Granule for pest control Pending JPH03261704A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2060582A JPH03261704A (en) 1990-03-12 1990-03-12 Granule for pest control

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2060582A JPH03261704A (en) 1990-03-12 1990-03-12 Granule for pest control

Publications (1)

Publication Number Publication Date
JPH03261704A true JPH03261704A (en) 1991-11-21

Family

ID=13146379

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2060582A Pending JPH03261704A (en) 1990-03-12 1990-03-12 Granule for pest control

Country Status (1)

Country Link
JP (1) JPH03261704A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TR26842A (en) * 1991-12-06 1994-08-19 Rhone Poulenc Agrochimie New agrochemical compounds containing both an active fungicidal material and an active insecticidal material for the preservation of nebulae.
US8232261B2 (en) 2003-07-18 2012-07-31 Bayer Cropscience Lp Method of minimizing herbicidal injury

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TR26842A (en) * 1991-12-06 1994-08-19 Rhone Poulenc Agrochimie New agrochemical compounds containing both an active fungicidal material and an active insecticidal material for the preservation of nebulae.
US8232261B2 (en) 2003-07-18 2012-07-31 Bayer Cropscience Lp Method of minimizing herbicidal injury
US8426339B2 (en) 2003-07-18 2013-04-23 Bayer Cropscience Lp Method of minimizing herbicidal injury

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