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JPH01175907A - Herbicidal composition - Google Patents

Herbicidal composition

Info

Publication number
JPH01175907A
JPH01175907A JP62330168A JP33016887A JPH01175907A JP H01175907 A JPH01175907 A JP H01175907A JP 62330168 A JP62330168 A JP 62330168A JP 33016887 A JP33016887 A JP 33016887A JP H01175907 A JPH01175907 A JP H01175907A
Authority
JP
Japan
Prior art keywords
weeds
compound
herbicidal composition
chloro
methyl
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
JP62330168A
Other languages
Japanese (ja)
Inventor
Yuji Enomoto
榎本 祐司
Yasunobu Funakoshi
船越 安信
Toshio Nanpo
南保 俊夫
Sadafumi Eda
貞文 江田
Masahiro Sakakibara
昌弘 榊原
Haruo Muto
武藤 治雄
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.)
Mitsui Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu Chemicals Inc
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 Mitsui Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP62330168A priority Critical patent/JPH01175907A/en
Publication of JPH01175907A publication Critical patent/JPH01175907A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain a herbicidal composition, containing three kinds of specific active compounds used in combination and capable of synergistically enhancing herbicidal effects and exhibiting precise controlling effects even by using in any period from the initial emergence of weeds just after rice transplanting to the season without phytotoxicity to paddy rice. CONSTITUTION:A herbicidal composition, obtained by blending (A) 3-chloro-4- methyl-6-(N-2-chloro-2-propenyl-N-phenylamino)pyridazine with (B) methyl 2-[3-(4,6-dimethoxypyrimidin-2-yl)ureidosulfonylmethyl]benzoate and (C) 3,7- dichloro-8-carboxyl-quinoline as active ingredients at 1:0.02-0.2:0.03-0.5 weight ratio (A:B:C) and useful as a herbicide for paddy field having the above- mentioned effects favorable from the view point of environmental pollution, since all the weeds can be controlled at a time by spraying small amounts of the chemicals which are incapable of controlling the weeds at all using the individual chemicals.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は3−クロロ−4−メチル−6−(N−2−クロ
ロ−2−プロペニル−N−フェニルアミノ)ピリダジン
(以下化合1lffAと略す)、メチル−2−(3−(
4,6−ジメトキシピリミジン−2−イル)ウレイドス
ルフォニルメチル〕ベンゾエート(以下化合物Bと略す
)及び3.7−ジクロロ−8−カルボキシ−キノリン(
以下化合物Cと略す)を有効成分として含有することを
特徴とする除草用組成物に間する。
Detailed Description of the Invention [Industrial Application Field] The present invention relates to 3-chloro-4-methyl-6-(N-2-chloro-2-propenyl-N-phenylamino)pyridazine (hereinafter abbreviated as compound 1lffA). ), methyl-2-(3-(
4,6-dimethoxypyrimidin-2-yl)ureidosulfonylmethyl]benzoate (hereinafter abbreviated as compound B) and 3,7-dichloro-8-carboxy-quinoline (
A herbicidal composition is characterized in that it contains a compound (hereinafter abbreviated as compound C) as an active ingredient.

本発明に係る除草用組成物は、水田用除草剤として農業
上有用である。
The herbicidal composition according to the present invention is agriculturally useful as a herbicide for paddy fields.

〔従来技術〕[Prior art]

我国の水田用除草剤は使用時期の面から、初期用除草剤
、−全処理剤、中期用除草剤の3つに大別されるが、前
二者で使用量の大半を占めている。
Herbicides for paddy fields in Japan are roughly divided into three categories based on the timing of use: initial herbicides, -all-treatment herbicides, and mid-term herbicides, but the first two account for the majority of the amount used.

初期用除草剤としては、2,4.6− )ジクロロフェ
ニルー4−ニトロフェニルエーテル及び2.4−ジクロ
ロフェニル−4−二トロー3−メトキシフェニルエーテ
ルが、又中期用除草剤としては、S−(4−クロロベン
ジル) −N、N−ジエチルチオールカーバメートと2
−メチルチオ−4,6−ビス(エチルアミノ)−S−)
リアジンとの混合剤、S−エチルN、N−へキサメチレ
ンチオールカーバメートと2−メチルチオ−4,6−ビ
ス(エチルアミノ)−3−トリアジンとT−(2−メチ
ル−4−クロロフェノキシ)酪酸エチルエステルとの混
合剤、又、−全処理剤としては2−クロロ−2’、6’
−ジエチル−N−(ブトキシメチル)−アセトアニリド
と4−(2,4−ジクロロベンゾイル) −1゜3−ジ
メチルピラゾール−5−イル−P−)ルエンスルホネー
トとの混合剤、2−(2−ナフトキシ)プロピオンアニ
リドと2−ベンゾチアゾール−2−イルオキシ−N−メ
チルアセトアニリドとN−(1,1−ジメチルベンジル
)−2−プロモーtert−ブチルアセトアミドとの混
合剤等がある。
Early stage herbicides include 2,4,6-)dichlorophenyl-4-nitrophenyl ether and 2,4-dichlorophenyl-4-nitro-3-methoxyphenyl ether, and mid-stage herbicides include S-( 4-chlorobenzyl) -N,N-diethylthiol carbamate and 2
-methylthio-4,6-bis(ethylamino)-S-)
Mixture with riazine, S-ethyl N,N-hexamethylenethiol carbamate and 2-methylthio-4,6-bis(ethylamino)-3-triazine and T-(2-methyl-4-chlorophenoxy)butyric acid A mixture with ethyl ester, or as a total treatment agent, 2-chloro-2',6'
-Mixture of diethyl-N-(butoxymethyl)-acetanilide and 4-(2,4-dichlorobenzoyl)-1゜3-dimethylpyrazol-5-yl-P-)luenesulfonate, 2-(2-naphthoxy ) A mixture of propionanilide, 2-benzothiazol-2-yloxy-N-methylacetanilide, and N-(1,1-dimethylbenzyl)-2-promo-tert-butylacetamide, etc.

又、これらの除草剤は多年生雑草に対する効果が充分で
なく、さらに温度、土壌、水管理等の条件によっては効
果の低下や水稲への薬害の発生をきたす事もしばしば見
られる。近年では農作業の省力化の点からも、−回の処
理によって多年生雑草を含めたすべての雑草を防除でき
て、しかも使用適期幅が広く、水稲に無害な除草剤の出
現が望まれている。しかし既存除草剤はこの様な要求を
満足しているとは言えない。
Furthermore, these herbicides are not sufficiently effective against perennial weeds, and depending on conditions such as temperature, soil, and water management, they often reduce their effectiveness or cause chemical damage to paddy rice. In recent years, from the perspective of saving labor in agricultural work, there has been a desire for a herbicide that can control all weeds, including perennial weeds, in two treatments, has a wide range of suitable periods for use, and is harmless to paddy rice. However, existing herbicides cannot be said to satisfy these requirements.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

本発明はこれらの要望に合致した、田植直後の雑草発生
始期から生育期までの任意の時期に使用して的確な防除
効果を有し、かつ水稲に無害な除草用組成物を提供する
事を目的とする。
The present invention meets these demands and provides a herbicidal composition that can be used at any time from the onset of weed emergence immediately after rice planting to the growing season, has an accurate control effect, and is harmless to paddy rice. purpose.

〔問題点を解決するための手段および作用〕化合物Aは
特開昭60−185768号公報に、化合物Bは特開昭
57−112379号公報に、化合物Cは特開昭57−
165368号公報に開示されている。それらの活性化
合物を各々単独で使用した場合、除草活性は常に充分満
足できるものではなく使用できる車種、適期は限定され
、雑草を防除できるように薬量を高く設定すると水稲に
対する薬害がしばしば見受けられる。すなわち、化合物
Aはホタルイ、タマガヤツリに対して高い効果があり、
つぎにタイヌビエ、ミズガヤツリに対して効果があるが
、オモダカ、ウリカワには効果を示さない。化合物Bは
、−年生広葉雑草及びウリカワ、オモダカに対しては高
い除草効果があるが、マツバイ、ホタルイ、ミズガヤツ
リに対しては除草効果が低い。
[Means and actions for solving the problems] Compound A is described in JP-A-60-185768, compound B is described in JP-A-57-112379, and compound C is described in JP-A-57-112379.
It is disclosed in Japanese Patent No. 165368. When these active compounds are used alone, their herbicidal activity is not always fully satisfactory, and the types of vehicles and suitable periods for which they can be used are limited, and when the dosage is set high to control weeds, chemical damage to paddy rice is often observed. . In other words, Compound A has a high effect on firefly and cypress,
Next, it is effective against Japanese grasshopper and Japanese cyperus, but it is not effective against Omodaka and Urikawa. Compound B has a high herbicidal effect on annual broad-leaved weeds, porphyry, and staghorn weeds, but has a low herbicidal effect on pine weeds, bulrushes, and cypresses.

化合物Cは、タイヌビエに対して高い除草効果があるが
、マツバイ、ミズガヤツリ及び広葉雑草に除草効果が低
い。また、いずれの化合物も雑草の葉令が進むとその効
果は急激に低下することが知られている。また、それぞ
れの単剤ではいずれも使用時期によっては水稲に対する
薬害の心配がある。
Compound C has a high herbicidal effect on Japanese millet, but has a low herbicidal effect on Japanese grasshopper, Japanese cypress, and broad-leaved weeds. Furthermore, it is known that the effectiveness of any compound decreases rapidly as the leaf stage of the weed advances. Furthermore, with each single agent, there is a concern that it may cause chemical damage to paddy rice depending on when it is used.

本発明者らは前記問題点を解決するため鋭意検討した結
果、化合物A、B及びCを混合使用すると個々の活性化
合物で防除困難な雑草に対して補足しあうばかりでなく
、各化合物の相乗的除草効果により各活性化合物単独で
は側底防除する事ができない様な少量の薬量で、−年生
雑草はもちろん最近多発化してきている多年生雑草に対
してかなり葉令が進んでも顕著な防除効果を示し、しか
も田植直後から生育期までの全期間に渡り、水稲に対す
る薬害がないという予想外、かつ驚くべき効果を示すこ
とを見出し本発明を完成した。
As a result of intensive studies to solve the above problems, the present inventors found that when compounds A, B, and C are used in combination, they not only complement each other against weeds that are difficult to control with the individual active compounds, but also synergize with each other. Due to its targeted herbicidal effect, each active compound can be used in small doses that would not be able to control the lateral side by itself, and has a remarkable control effect on not only annual weeds but also perennial weeds, which have recently become more common, even when they are quite advanced in leaf age. We have completed the present invention by discovering that it exhibits an unexpected and surprising effect of not causing chemical damage to paddy rice over the entire period from immediately after rice planting to the growing season.

すなわち、本発明は3−クロロ−4−メチル−6−(N
−2−クロロ−2−プロペニル−N−フェニルアミノ)
ピリダジン、メチル−2−(3−(4,6−ジメトキシ
ピリミジン−2−イル)ウレイドスルフォニルメチル〕
ベンゾエート及ヒ3.7−ジクロロ−8−カルボキシ−
キノリンを有効成分として含有することを特徴とする除
草用組成物である。
That is, the present invention provides 3-chloro-4-methyl-6-(N
-2-chloro-2-propenyl-N-phenylamino)
Pyridazine, methyl-2-(3-(4,6-dimethoxypyrimidin-2-yl)ureidosulfonylmethyl)
Benzoate and H3,7-dichloro-8-carboxy-
This is a herbicidal composition characterized by containing quinoline as an active ingredient.

本発明に係る除草用組成物はある組成比率にて特に強力
な相乗効果をあられすが、3種の活性化合物の混合割合
はかなり広い範囲内で変化してよい。
Although the herbicidal compositions according to the invention exhibit a particularly strong synergistic effect in certain composition ratios, the mixing proportions of the three active compounds may vary within a fairly wide range.

具体的には化合物A1重量部に対し、化合物80102
〜0.2重量部、化合物CO,03〜0.5重量部であ
り、化合物A1重量部に対し化合物80.04〜0.1
3重量部、化合物CO,06〜0.3重量部とするのが
より望ましい。
Specifically, compound 80102 to 1 part by weight of compound A
~0.2 part by weight, 0.3 to 0.5 part by weight of compound CO, and 80.04 to 0.1 part by weight of compound A to 1 part by weight of compound A.
More preferably, the amount is 3 parts by weight, and the amount of the compound CO is 06 to 0.3 parts by weight.

本発明に係る除草用組成物は、通常は担体及び必要に応
じて他の補助剤を添加混合して、製剤形態、たとえば粒
剤、粉剤、水和剤、フロアブル剤等に調製して使用する
。担体としては、クレー類、タルク、ベントナイト、ケ
イソウ土、ホワイトカーボン、炭酸カルシウム、ゼオラ
イト、無水ケイ酸等の無機物質;小麦粉、大豆粉、デン
プン、結晶セルロース等の植物性有機物質;ポリ塩化ビ
ニル、石油樹脂、ポリアルキレングリコール等の高分子
化合物;尿素;ワックス類等が挙げられる。
The herbicidal composition according to the present invention is usually used by adding and mixing a carrier and other adjuvants as necessary to form a formulation such as granules, powders, wettable powders, flowables, etc. . Examples of carriers include inorganic substances such as clays, talc, bentonite, diatomaceous earth, white carbon, calcium carbonate, zeolite, and silicic anhydride; vegetable organic substances such as wheat flour, soy flour, starch, and crystalline cellulose; polyvinyl chloride, Polymer compounds such as petroleum resins and polyalkylene glycols; urea; waxes and the like can be mentioned.

また、液体担体としては各種オイル類、有機溶剤及び水
等が挙げられる。
In addition, examples of the liquid carrier include various oils, organic solvents, water, and the like.

更に、製剤上必要とされる補助剤としては、各種界面活
性剤やゼラチン、アルブミン、アルギン酸ナトリウム、
メチルセルロース、カルボキシメチルセルロース、ポリ
ビニルアルコール、キサンタンガム等の高分子化合物や
その他の補助剤が挙げられる。界面活性剤としては、各
種の非イオン性や陰イオン性界面活性剤が挙げられるが
、時には陽イオン性や両性イオン界面活性剤が用いられ
〔実施例〕 次に本発明に係る除草用組成物の実施例を挙げて説明す
るが、本発明はこれのみに限定されるものではない。
Furthermore, auxiliary agents required for formulation include various surfactants, gelatin, albumin, sodium alginate,
Examples include polymeric compounds such as methylcellulose, carboxymethylcellulose, polyvinyl alcohol, and xanthan gum, and other auxiliary agents. Examples of the surfactant include various nonionic and anionic surfactants, but cationic and amphoteric surfactants are sometimes used [Example] Next, the herbicidal composition according to the present invention The present invention will be described with reference to examples, but the present invention is not limited thereto.

なお、実施例中の混合割合はすべて重量比である。In addition, all the mixing ratios in the examples are weight ratios.

実施例1 粒 剤 化合物A 4z、化合物80.17! 、化合物C1z
、ベントナイトとタルクの混合物(7: 3)91.8
3χ、アルキルナフタリンスルホン酸縮合物2z及びジ
オクチルスルホサクシネート1χを混合した後、適量の
水を加えて混練し、造粒機を用いて通常の方法で造粒し
粒剤とした。
Example 1 Granule Compound A 4z, Compound 80.17! , compound C1z
, mixture of bentonite and talc (7:3) 91.8
After mixing 3χ, alkylnaphthalene sulfonic acid condensate 2z, and dioctyl sulfosuccinate 1χ, an appropriate amount of water was added and kneaded, and the mixture was granulated using a granulator in a conventional manner to obtain granules.

実施例2 粒 剤 化合物A5χ、化合物B0.25K、化合物co、sy
t、ベントナイトとタルクの混合物(7: 3) 92
.95χ及びリグニンスルホン酸ナトリウム1χを混合
した後、適量の水を加えて混練し、造粒機を用いて通常
の方法で造粒し粒剤とした。
Example 2 Granules Compound A5χ, Compound B0.25K, Compound co, sy
t, mixture of bentonite and talc (7:3) 92
.. After mixing 95χ and sodium ligninsulfonate 1χ, an appropriate amount of water was added and kneaded, and the mixture was granulated using a granulator in a conventional manner to obtain granules.

実施例3 粒 剤 化合物A 6z、化合物80.17χ、化合物C0,5
!、クレー89.33χ、アルキルベンゼンスルホン酸
ナトリウム2χ及びカルボキシメチルセルロース2χを
均一に粉砕、混合した後適量の水を加えて混練し、造粒
機を用いて通常の方法により造粒し粒剤とした。
Example 3 Granules Compound A 6z, Compound 80.17χ, Compound C0,5
! , clay 89.33χ, sodium alkylbenzenesulfonate 2χ and carboxymethylcellulose 2χ were uniformly ground and mixed, then kneaded with an appropriate amount of water, and granulated using a granulator in a conventional manner to obtain granules.

以下、試験例により本発明に係る除草用組成物の除草効
果を具体的に説明する。
Hereinafter, the herbicidal effect of the herbicidal composition according to the present invention will be specifically explained using test examples.

試験例1 雑草発芽始期における除草試験水田用土壌を
1/2.0007−ル ヮグネルボントに入れ、これに
N、 P、O5およびKzOとして各1gを含む化成肥
料で全層に施肥し、適量の水を加えて充分にかきまぜ湛
水状態とする。予め温室で生育させた水稲苗(葉令2.
5)の2本を一株とし、ポット当りその2株を深さ3c
1!にそう苗して、これにタイヌビエ、ホタルイ、コナ
ギの種子を播種した。また、これにオモダカ、クログワ
イ及びウリカワの塊茎を移植し、湛水法3CI11に保
ちながら温室で生育させた。
Test Example 1 Weeding test at the beginning of weed germination Paddy soil was placed in a 1/2.0007-Lugnerbont, and the entire layer was fertilized with a chemical fertilizer containing 1 g each of N, P, O5, and KzO, and an appropriate amount of water was added. Add water and stir thoroughly to make it submerged. Paddy rice seedlings grown in advance in a greenhouse (leaf age 2.
5) are considered as one plant, and the two plants per pot are placed at a depth of 3c.
1! I planted seedlings, and then sowed seeds of Japanese cabbage, firefly, and Konagi. In addition, tubers of Omodaka, Kurogwai, and Urikawa were transplanted to this, and grown in a greenhouse while being maintained at submergence method 3CI11.

そう苗10日後雑草発生始期に供試化合物の所定量を前
記実施例に示した方法に準じて製剤した粒剤を用いて処
理した。処理後は1日あたり1cmの漏水を与えた。薬
剤処理1ケ月後に除草効果及び水稲の薬害について調査
した。その結果を次の第1表に示す。
After 10 days from the seedlings, at the beginning of weed emergence, a predetermined amount of the test compound was treated using granules prepared according to the method shown in the above example. After treatment, water leakage of 1 cm per day was allowed. One month after the chemical treatment, the herbicidal effect and chemical damage to paddy rice were investigated. The results are shown in Table 1 below.

この表中で各草種に対する除草効果と薬害は下記の評価
基準に従い、「0」から「9」までの10段階の数値を
用いて表わした。
In this table, the herbicidal effects and phytotoxicity of each grass species are expressed using a 10-level numerical value from "0" to "9" according to the following evaluation criteria.

評価基準 0 残草量対無処理比  85以上(重量%)1   
       71〜84 2          56〜70 3          41〜55 4          31〜40 5          21〜30 6          11〜20 7          6〜10 8          1〜5 水稲に対する薬害程度の表示区分は「菌寄」、「人害」
、r中寄」、「小書」、「微官」及び「無害」の6段階
とした。
Evaluation criteria 0 Remaining grass amount to no treatment ratio 85 or more (weight%) 1
71-84 2 56-70 3 41-55 4 31-40 5 21-30 6 11-20 7 6-10 8 1-5 The classification of chemical damage to paddy rice is "fungal infection" and "human damage"
There were six levels: ``, nakayori'', ``small book'', ``minor'', and ``harmless''.

無害: 薬害症状なし 微官:′回復大 小書: 減収予g5%以下 中寄:  〃  6〜15χ 人害:〃16〜30χ 菌寄:〃31%以上 第1表の結果より次の事が明らかである。市販剤りでは
、雑草発生始期でオモダカ、クログワイを防除できない
、一方、化合物A、B、C各単剤ではオモダカ、クログ
ワイ、ウリカワを完全には防除できない薬量で、A/B
/C3化合物を組合せることにより全草種を防除できる
Harmless: No drug-induced symptoms Minor symptoms: ``Recovery: Expected decrease in yield g 5% or less Medium-sized: 〃 6-15χ Human damage: 〃 16-30χ Bacterial infection: 〃 31% or more The following is clear from the results in Table 1. It is. Commercially available pesticides cannot control Omodaka and Kurogai at the beginning of weed emergence, while compounds A, B, and C alone cannot completely control Omodaka, Kurogwai, and Urikawa at dosages A/B.
/C3 compounds can control all plant species.

また、化合物B/Cの組合せでは殺草スペクトラムが不
充分でホタルイ、オモダカ、クログワイという強害雑草
が残るが、本発明のA/B/C3化合物の混合剤では全
草種を防除できる。
In addition, the combination of compounds B/C has an insufficient herbicidal spectrum and leaves harmful weeds such as firefly, omodaka, and black weed, but the mixture of A/B/C3 compounds of the present invention can control all plant species.

第1表 イ   ホ   コ   オ   り   ウ   薬
化合物   薬 量   ヌ  タ  す  モ  ロ
  リビ  ル  ギ  ダ  グ  カ ai g/a     エ   イ       カ 
  ワ   ヮイ        害 化合物A    2    022020  無5  
     196090    〃化合物B0.113
5222   〃 0.3478668    〃 化合物C2402000〃 5       918100    〃化合物B/C
O,1/2   3  3  5  2  2  4 
  〃0.315     9    7    9 
   6    6    8    〃化合物A/B
/C210,1/2  9  9  9  9  9 
 9   〃看1店U円D     取部%     
 9    8    9    4    2   
 8    〃市販剤り:2−クロロー2′、6”−ジ
エチル−N−(ブトキシメチル)アセトアニリド2.5
χ、4−(2,4−ジクロロベンゾイル)−1,3−ジ
メチル−5−ピラゾリル−P−)ルエンスルホネート 
6χ 試験例2 圃場試験 水田一般雑草が自然混在している水田を、通常の方法で
耕起、施肥(N、 PKO5+ KtOとして各IKg
/アール)、代かき及び整地を行い、−区10ホ(2,
5sX4a+ )に区画し、これに葉令2.5の水稲稚
苗2本を一株として畦間隔30C11、横間隔15C1
1で移植した。移植後は湛水法を3〜5〔に保ちながら
雑草発芽始期(田植3日後)及びタイヌビエの3.0〜
3.5葉期(田植15′日後)に前記実施例に示した方
法に準じて調製した供試化合物の混合剤または単剤粒剤
を手まきで撒布した。撒布1ケ月後の雑草量および4ケ
月後の水稲の収量を調査し、その結果を第2表に示す。
Table 1 Drug Compound Dosage
Wow Harmful Compound A 2 022020 No 5
196090 Compound B0.113
5222 0.3478668 Compound C2402000 5 918100 Compound B/C
O, 1/2 3 3 5 2 2 4
〃0.315 9 7 9
6 6 8 Compound A/B
/C210,1/2 9 9 9 9 9
9 〃1 store U yen D Toribe%
9 8 9 4 2
8 Commercially available agent: 2-chloro2',6''-diethyl-N-(butoxymethyl)acetanilide 2.5
χ,4-(2,4-dichlorobenzoyl)-1,3-dimethyl-5-pyrazolyl-P-)luenesulfonate
6χ Test Example 2 Field Test Paddy Field A paddy field in which general weeds are naturally mixed was plowed and fertilized in the usual way (N, PKO5 + KtO, each IKg)
/ R), plowing and leveling the land, - Ward 10 Ho (2,
5sX4a+), and two paddy rice seedlings of leaf age 2.5 are placed as one plant with a row spacing of 30C11 and a horizontal spacing of 15C1.
I transplanted it with 1. After transplanting, keep the waterlogging method at 3 to 5 [at the beginning of weed germination (3 days after rice planting) and 3.0 to 3.0 for Japanese millet.
At the 3.5 leaf stage (15' days after rice planting), a mixture or single granule of the test compound prepared according to the method shown in the above example was spread by hand. The amount of weeds one month after sowing and the yield of paddy rice four months later were investigated, and the results are shown in Table 2.

第2表の結果より市販剤りは薬量300g/aで田植5
日後処理ではタイヌビエ、ホタルイ、コナギ、ウリカワ
は浅草量5%以下であり、はとんど完全に防除できるが
、クログワイ、オモダカは防除できていない。しかるに
本発明の3化合物混合剤は化合物A2g/a、化合物8
0.05g/a及び化合物01 g/aの組合わせでも
、単剤では防除できない雑草を完全に防除できる。
From the results in Table 2, the commercially available agent has a dosage of 300g/a and a rice transplant rate of 5.
After a day's treatment, the amount of grasses that account for less than 5% of Japanese grasshopper, firefly, Konagi, and Urikawa can be almost completely controlled, but Black-capped Gray Wig and Omodaka cannot be controlled. However, the three-compound mixture of the present invention contains 2 g/a of compound A and 8 g/a of compound A.
Even a combination of 0.05 g/a and Compound 01 g/a can completely control weeds that cannot be controlled with a single agent.

田植15日後という、かなり雑草の生育が進んだ時期の
処理では、市販剤りでは雑草をほとんど防除できず、同
様に化合物A15g/a 、化合物B O,2g/a及
び化合物C4g/aの各単剤では防除できない雑草があ
るが、A/B/C3化合物を組合わせると驚くほど高い
防除効果を示し、かつ−年生雑草だけでなく多年生雑草
まで防除できることが明らかである。
When treated 15 days after rice planting, when the growth of weeds is considerably advanced, commercially available pesticides are hardly able to control weeds; Although there are some weeds that cannot be controlled with chemical agents, it is clear that the combination of A/B/C3 compounds shows a surprisingly high control effect and can control not only annual weeds but also perennial weeds.

〔発明の効果〕〔Effect of the invention〕

以上の結果から明らかなように本発明に係る除草用組成
物は、田植直後の雑草の発芽始期から最盛期までいずれ
の時期に使用しても水稲に対しては無害で、しかも3種
の薬剤の相剰作用により個々の薬剤では防除できない薬
量を用い、1回の撒布ですべての雑草を防除でき、環境
汚染の面からも好ましい除草剤であり、従来多く使用さ
れている除草剤に較べて著しく優れている。
As is clear from the above results, the herbicidal composition according to the present invention is harmless to paddy rice even when used at any time from the beginning of weed germination to the peak of weed growth immediately after rice transplantation, and is effective against three types of chemical agents. Due to the synergistic effect of the two, it is possible to control all weeds in a single application using a dosage that cannot be controlled by each individual agent, making it a preferable herbicide from the standpoint of environmental pollution, compared to the herbicides commonly used in the past. It is extremely superior.

Claims (2)

【特許請求の範囲】[Claims] (1)3−クロロ−4−メチル−6−(N−2−クロロ
−2−プロペニル−N−フェニルアミノ)ピリダジン、
メチル−2−〔3−(4,6−ジメトキシピリミジン−
2−イル)ウレイドスルフォニルメチル〕ベンゾエート
及び3,7−ジクロロ−8−カルボキシ−キノリンを有
効成分として含有することを特徴とする除草用組成物。
(1) 3-chloro-4-methyl-6-(N-2-chloro-2-propenyl-N-phenylamino)pyridazine,
Methyl-2-[3-(4,6-dimethoxypyrimidine-
A herbicidal composition comprising 2-yl)ureidosulfonylmethyl]benzoate and 3,7-dichloro-8-carboxy-quinoline as active ingredients.
(2)3−クロロ−4−メチル−6−(N−2−クロロ
−2−プロペニル−N−フェニルアミノ)ピリダジン、
メチル−2−〔3−(4,6−ジメトキシピリミジン−
2−イル)ウレイドスルフォニルメチル〕ベンゾエート
及び3,7−ジクロロ−8−カルボキシ−キノリンの割
合が1:0.02〜0.2:0.03〜0.5(重量比
)であることを特徴とする特許請求の範囲第1項記載の
除草用組成物。
(2) 3-chloro-4-methyl-6-(N-2-chloro-2-propenyl-N-phenylamino)pyridazine,
Methyl-2-[3-(4,6-dimethoxypyrimidine-
2-yl)ureidosulfonylmethyl]benzoate and 3,7-dichloro-8-carboxy-quinoline in a ratio of 1:0.02 to 0.2:0.03 to 0.5 (weight ratio) The herbicidal composition according to claim 1.
JP62330168A 1987-12-28 1987-12-28 Herbicidal composition Pending JPH01175907A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62330168A JPH01175907A (en) 1987-12-28 1987-12-28 Herbicidal composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62330168A JPH01175907A (en) 1987-12-28 1987-12-28 Herbicidal composition

Publications (1)

Publication Number Publication Date
JPH01175907A true JPH01175907A (en) 1989-07-12

Family

ID=18229580

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62330168A Pending JPH01175907A (en) 1987-12-28 1987-12-28 Herbicidal composition

Country Status (1)

Country Link
JP (1) JPH01175907A (en)

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