JPH01242506A - Herbicide composition - Google Patents

Herbicide composition

Info

Publication number
JPH01242506A
JPH01242506A JP6731688A JP6731688A JPH01242506A JP H01242506 A JPH01242506 A JP H01242506A JP 6731688 A JP6731688 A JP 6731688A JP 6731688 A JP6731688 A JP 6731688A JP H01242506 A JPH01242506 A JP H01242506A
Authority
JP
Japan
Prior art keywords
herbicide
bromobutide
amount
weeds
synmethrin
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
Application number
JP6731688A
Other languages
Japanese (ja)
Other versions
JP2549142B2 (en
Inventor
Nozomi Kaizan
海山 望
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.)
SHELL KAGAKU KK
Original Assignee
SHELL KAGAKU KK
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 SHELL KAGAKU KK filed Critical SHELL KAGAKU KK
Priority to JP6731688A priority Critical patent/JP2549142B2/en
Publication of JPH01242506A publication Critical patent/JPH01242506A/en
Application granted granted Critical
Publication of JP2549142B2 publication Critical patent/JP2549142B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE:To obtain a herbicide showing extremely excellent synergistic effects on gramineous weeds and cyperaceous weeds, capable of reducing phytotoxicity to crops because of enabling of remarkable reduction in amount of herbicide, containing cinmethylin and bromobutide in a specific ratio. CONSTITUTION:A herbicide composition obtained by blending 1 pt.wt. cinmethylin shown by formula I with 1-20 pts.wt. bromobutide shown by formula II, surfactant, solid carrier, binder, etc. and made into granules by aggregation method or impregnation method or into a form such as wettable powder or paste. The herbicide has not only excellent effects on weeds in paddy fields such as Echinochloa oryzicola Vasing, Echinochloa crus-galli Beauv. var. praticola Ohwi., monochoria, water nutgrass, slender spikerush, etc., but also can reduce the amount of herbicide because of synergistic effects by blending. Treatment period of the herbicide is suitably prior to germination to early stage of growth.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は水田の雑草の防除に有効な除草剤組成物に関す
る。更に詳しくは本発明は、有効成分として A、(±)−2−エキンー(2−メチルベンジルオキシ
)−1−メチル−4−イソプロピル−7−オキサビシク
ロ[2,2,11へブタン(以下シンメスリンと呼ぶ。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a herbicidal composition effective for controlling weeds in rice fields. More specifically, the present invention uses A, (±)-2-echin-(2-methylbenzyloxy)-1-methyl-4-isopropyl-7-oxabicyclo[2,2,11 hebutane (hereinafter referred to as synmethrin) as an active ingredient. It is called.

)及び B、(R3)−2−プClモーN−(、、、−ジメチル
ベンジル)−3,3−ジメチルブチルアミド(以下ブロ
モブチドという。) を含有する混合除草剤組成物に関する。
) and B, (R3)-2-ClMoN-(,,,-dimethylbenzyl)-3,3-dimethylbutyramide (hereinafter referred to as bromobutide).

[従来の技術および発明が解決しようとする課題J(±
)−2−エキソ−(2−メチルベンジルオキシ)−1−
メチル−4−イソプロピル−7−オキサビシクロ[2,
2,l]へブタンは下記の構造を有する化合物であり、 一般名シンメスリンとして知られている。
[Problems to be solved by the conventional technology and invention J (±
)-2-exo-(2-methylbenzyloxy)-1-
Methyl-4-isopropyl-7-oxabicyclo[2,
2,l] Hebutane is a compound having the following structure and is known by the generic name synmethrin.

その製法、除草特性は特開昭58−110591号公報
に記載されており、イネ科、カヤツリグサ科、オモダカ
科、ミズアオイ科などの単子葉雑草に対し、極めて少量
の処理量で有効な除草作用を有する。例えば最も感受性
の高いノビエに対して発芽時では1ヘクタール当り僅か
10gの処理量で有効な除草効果を示す。また1、5葉
のノビエに対しては20g/ヘクタール、2.0葉のノ
ビエに対し45g/ヘクタール、2.5葉のノビエに対
し60g/ヘクタール、3.0葉のノビエに対し90g
/ヘククールの処理量で有効である。
Its manufacturing method and herbicidal properties are described in JP-A-58-110591, and it has an effective herbicidal effect on monocotyledonous weeds such as Poaceae, Cyperaceae, Omodacaceae, and Polygonaceae with an extremely small amount of treatment. have For example, a treatment amount of only 10 g per hectare is effective against weeds, which are the most susceptible, at the time of germination. Also, 20g/ha for wildflowers with 1 and 5 leaves, 45g/ha for wildflowers with 2.0 leaves, 60g/ha for wildflowers with 2.5 leaves, and 90g/ha for wildflowers with 3.0 leaves.
/Effective with a throughput of Hekucool.

また水稲に対する安全性は気象、土壌条件、水稲の生育
状態などによって変動するが、その限界は1ヘクタール
尚り609から120gである。
Furthermore, the safety for paddy rice varies depending on the weather, soil conditions, growth conditions of paddy rice, etc., but the limit is 609 to 120 g per hectare.

一方、(R5)−2−ブロモ−N−(σ、σ−ジメチル
ベンジル)−3,3−ジメチルブチルアミドは下記の構
造を有する化合物であり、一般名プロモブチドとして知
られている水稲用除草剤である。
On the other hand, (R5)-2-bromo-N-(σ,σ-dimethylbenzyl)-3,3-dimethylbutyramide is a compound having the following structure, and is a herbicide for rice rice commonly known as promobutide. It is.

ブロモブチドの製法及び除草特性は特公昭56−434
55号公報に記載されており、カヤツリグサ科、ミズア
オイ科、ゴマノハグ”l’ltミソ”ギ科、ミズハコベ
科、オモダカ科等の雑草の防除に有効であり、特にカヤ
ツリグサ科のホタルイに対し、比較的低薬量で有効な除
草効果を有する。
The manufacturing method and herbicidal properties of bromobutide were published in Japanese Patent Publication No. 56-434.
It is described in Publication No. 55 and is effective in controlling weeds such as Cyperaceae, Cyperaceae, Cyperaceae, Cyperaceae, Cyperaceae, and Omodaceae, and is relatively effective against firefly of the Cyperaceae family. It has an effective herbicidal effect at low doses.

例えば発芽期のホタルイに対しては100〜200y/
ヘクタール、■、0〜1.5葉期のホタルイに対して2
50g/ヘクタール、2.5〜3.0葉期では500g
/ヘクタール、の処理量で有効な除草効果を発揮する。
For example, for firefly in the germination period, 100 to 200 y/
ha, ■, 2 for firefly at 0-1.5 leaf stage
50g/ha, 500g at 2.5-3.0 leaf stage
Demonstrates effective weed control at a treatment rate of /ha.

しかしながら葉令の進んだタイヌビエに対しては効果が
低下する傾向が認められた。
However, there was a tendency for the effectiveness to decrease against Japanese millet with advanced leaf stages.

近年除草剤のめざましい進歩により、選択性の優れた除
草剤が開発されたが、一方防除を必要とする雑草の種類
も多く、これらをすべて防除するためには数種の除草剤
の混合が必要となってくる。
In recent years, remarkable advances in herbicides have led to the development of highly selective herbicides, but on the other hand, there are many types of weeds that need to be controlled, and in order to control them all, it is necessary to mix several types of herbicides. It becomes.

そのため使用量が増加し、それによって作物に対する薬
害の増加という問題が発生してくる。また除草剤の混合
使用によって作物への薬害が相乗効果で現れる場合もし
ばしばあるので除草剤の混合処方については特に綿密な
試験が必要である。
Therefore, the amount used increases, leading to the problem of increased phytotoxicity to crops. In addition, the use of mixed herbicides often causes synergistic effects on crops, so careful testing is especially necessary for mixed formulations of herbicides.

[課題を解決するための手段] 発明者は多種類の雑草に対し少量の薬量で有効な防除作
用を示し、薬害の少い混合除草剤の開発を続けた結果、
驚くべきことに、上記シンメスリン及びブロモブチドを
特定の割合で混合施用することにより、イネ科雑草及び
カヤツリグサ科雑草に対し、極めて顕著な相乗効果が得
られ、シンメスリン及びブロモブチド単剤の効果から予
測される使用量よりはるかに低薬量の混合によって上記
2種の単剤の効果を発揮させることができることを見出
した。しかも水稲への薬害の相乗効果は認められないの
で、混合除草剤組成物による低薬量処理により、水稲へ
の薬害を軽減することに成功し Iこ 。
[Means for Solving the Problems] As a result of continued development of a mixed herbicide that exhibits effective control action against many types of weeds with a small dose and has little chemical damage, the inventor has found that:
Surprisingly, by applying the above-mentioned synmethrin and bromobutide in a mixed manner at a specific ratio, a very significant synergistic effect was obtained against grass and cyperaceous weeds, which is expected from the effect of synmethrin and bromobutide alone. It has been found that the effects of the above-mentioned two types of single agents can be exhibited by mixing them in a much lower amount than the amount used. Moreover, since no synergistic effect of chemical damage to paddy rice was observed, we succeeded in reducing the chemical damage to paddy rice by low-dose treatment with a mixed herbicide composition.

すなわち本発明は A、(±)−2−エキンー(2−メチルベンジルオキシ
)−1−メチル−4−イングロビルー7−オキサビシク
口[2,2,1]へブタン(シンメスリン)及び、 B、(R5)−2−ブロモ−N−(a、a−ジメチルベ
ンジル)−3,3−ジメチルブチルアミド (ブロモブチド)有効成分として含有することを特徴と
する除草剤組成物である。
That is, the present invention provides A, (±)-2-equin-(2-methylbenzyloxy)-1-methyl-4-ingrobyl-7-oxabisic-[2,2,1]hebutane (synmethrin), and B, (R5 )-2-Bromo-N-(a,a-dimethylbenzyl)-3,3-dimethylbutyramide (bromobutide) as an active ingredient.

本発明除草剤組成物中のシンメスリンとブロモブチドの
混合比率は、好ましくはシンメスリン1重量部に対し、
ブロモブチド0.5〜200重量部であるが、特に好ま
しくは1〜20重量部である。
The mixing ratio of synmethrin and bromobutide in the herbicidal composition of the present invention is preferably 1 part by weight of synmethrin:
The amount of bromobutide is 0.5 to 200 parts by weight, particularly preferably 1 to 20 parts by weight.

シンメスリンとブロモブチドの混合は両者を混合粒剤と
して製剤し使用する方法が最も適しているが、水利剤、
ペーストなどの形態で混合使用することもできる。
The most suitable way to mix synmethrin and bromobutide is to formulate and use them as mixed granules,
They can also be mixed and used in the form of a paste or the like.

粒剤の製造は公知の方法で製造することができる。例え
ばシンメスリン、ブロモブチドの有効成分を界面活性剤
、固体担体、結合剤などと混合し、凝集法、含浸法など
により製造される。界面活性剤としては非イオン性、カ
チオン性、アニオン性、両性イオン性などいずれも使用
できる。例えばアルキル硫酸エステル、アルキルアリー
ルスルホン酸塩、ポリオキシエチレン脂肪酸エステル、
ポリオキシエチレン脂肪酸アルコールエーテルなどをあ
げることができる。固体担体としてはタルク、クレー、
ベントナイト、酸性白土、ピロフィライト、炭酸カルシ
ウム、方解石、硫酸アンモニウムなどをあげることがで
きる。
Granules can be manufactured by a known method. For example, active ingredients such as synmethrin and bromobutide are mixed with a surfactant, a solid carrier, a binder, etc., and produced by aggregation method, impregnation method, etc. As the surfactant, any of nonionic, cationic, anionic, and amphoteric ionic surfactants can be used. For example, alkyl sulfates, alkylaryl sulfonates, polyoxyethylene fatty acid esters,
Examples include polyoxyethylene fatty acid alcohol ether. Solid carriers include talc, clay,
Examples include bentonite, acid clay, pyrophyllite, calcium carbonate, calcite, and ammonium sulfate.

粒剤中の活性物質の量は0.1〜5重量%、好ましくは
0.2〜2.2重量%の範囲である。
The amount of active substance in the granules ranges from 0.1 to 5% by weight, preferably from 0.2 to 2.2% by weight.

本発明の除草剤組成物の処理期間としては雑草の発芽前
から生育初期が適しており、0〜3.0葉期までに処理
するのが望ましい。また水稲の苗の移植後3日〜20日
の期間が適しており、特に7日〜14日の間が最適であ
る。
The suitable period for treatment with the herbicide composition of the present invention is from before the germination of weeds to the early stage of growth, and it is desirable to apply the herbicide composition at the 0 to 3.0 leaf stage. Further, a period of 3 to 20 days after transplanting paddy rice seedlings is suitable, and a period of 7 to 14 days is particularly optimal.

除草剤組成物の使用投与量はシンメス9フ24ル60g
/ヘクタール、ブロモブチ1纏5〜60g/ヘクタール
、ブロモブチド45〜6009/ヘクタールの範囲とす
ることが好ましい。
The dosage of the herbicide composition used is 60g of Shinmeth 9F24F.
Preferably, the amount of bromobutide is 5 to 60 g/ha, and the amount of bromobutide is 45 to 6009 g/ha.

[発明の効果1 本発明の除草剤組成物はその構成成分であるシンメスリ
ン及びブロモブチドの特長が生かされ、タイヌビエ、ノ
ビエ、ホタルイ、コナギ、ミズガヤツリ、マツバイなど
多くの水田重要雑草に対し優れた防除効果を有するのみ
ならず、混合による相乗的除草効果を発揮し、それぞれ
の単独使用の場合に比べて著しい活性を示す。そのため
除草剤使用量の大巾な軽減が可能となり、作物に対する
薬害を減少することができる。
[Effect of the invention 1] The herbicidal composition of the present invention takes advantage of the characteristics of its constituent components, synmethrin and bromobutide, and has excellent control effects against many important weeds in paddy fields, such as Japanese grasshopper, Japanese field grass, bulrush, Japanese grasshopper, Japanese grasshopper, and Japanese grasshopper. Not only do they have a synergistic herbicidal effect when mixed, but they exhibit remarkable activity compared to when each is used alone. Therefore, it is possible to greatly reduce the amount of herbicides used, and it is possible to reduce chemical damage to crops.

また水稲に対する薬害の増加は認められないので極めて
安全性の高い除草剤組成物である。
Furthermore, since no increase in chemical damage to paddy rice was observed, it is an extremely safe herbicide composition.

以下に配合例及び試験例をあげて、本発明を更に説明す
る。
The present invention will be further explained with reference to formulation examples and test examples below.

配合例1 シンメスリン    0.1重量部(化合物100%換
算)ブロモブチド    1.5重量部(〃)ネオゲン
パウダー  1.O n (第一工業製薬(株)製陰イオン界面活性剤)ベントナ
イト    50.0// タルク       47.47/ を混合し、水を加え、混練した後、造粒乾燥して粒剤を
得た。
Formulation Example 1 Synmethrin 0.1 parts by weight (calculated as 100% compound) Bromobutide 1.5 parts by weight (〃) Neogen Powder 1. On (anionic surfactant manufactured by Daiichi Kogyo Seiyaku Co., Ltd.) bentonite 50.0// talc 47.47/ was mixed, water was added, kneaded, and then granulated and dried to obtain granules. .

配合例2 シンメスリン    2.0重量部(化合物100%換
算)ブロモブチド   40.0//(    // 
     )(吸着剤) クレー       43.0// をよく粉砕混和して水利剤を得た。
Formulation example 2 Synmethrin 2.0 parts by weight (calculated as 100% compound) Bromobutide 40.0 // ( //
) (Adsorbent) Clay 43.0// was thoroughly ground and mixed to obtain an irrigation agent.

試験例I (タイヌビエに対するシンメスリンとブロモブチドの相
乗的除草効果) [試験方法1 面積1/10,000アールのポットにタイヌビエのあ
らかじめ催芽せしめた種子10粒を深さ5mmに播種し
、水深3cmの水田状態に保った。
Test Example I (Synergistic herbicidal effect of synmethrin and bromobutide on Japanese millet) [Test method 1 Ten pre-germinated seeds of Japanese millet are sown to a depth of 5 mm in a pot with an area of 1/10,000 are, and a paddy field with a water depth of 3 cm is planted. kept in condition.

シンメスリン及びブロモブチドの7種の混合比率の除草
剤組成物をアセトンに溶解し、これを等量の水で希釈し
た除草剤組成物溶液を調製した。
A herbicide composition solution was prepared by dissolving seven herbicide compositions of synmethrin and bromobutide in acetone and diluting this with an equal amount of water.

更に各混合比率の組成物溶液について、これを水/アセ
トン等量混合液で各0.75倍の濃度に4段階に希釈し
た計5種の濃度の溶液を用意した。
Furthermore, the composition solutions of each mixing ratio were diluted in four stages with equal amounts of water/acetone to a concentration of 0.75 times each to prepare solutions with a total of five concentrations.

播種後12日のタイヌビエが2葉期に達した時、ポット
当り10m12の薬液をピペットにて滴下処理した。各
混合比率の薬液の基本処理量(希釈倍率Iの場合の処理
量)及び希釈倍率は次の通りである。
When the Japanese millet reached the two-leaf stage 12 days after sowing, 10 m12 of the chemical solution per pot was dripped with a pipette. The basic processing amount (processing amount in the case of dilution ratio I) and dilution ratio of the chemical solution at each mixing ratio are as follows.

試験は各混合比率、各濃度の薬液について、それぞれ3
反復で行われた。
The test consisted of 3 tests for each mixing ratio and each concentration of drug solution.
It was done iteratively.

処理後、必要に応じて肉眼による観察を行い、2週間後
にタイヌビエの本数と生体重を測定し、各混合比率での
処理について、5濃度、3反復の生体重の平均値を第1
表に示した。
After treatment, perform visual observation as necessary, measure the number and live weight of Japanese millet after 2 weeks, and calculate the average value of the fresh weight of 3 replicates at 5 concentrations for each treatment at each mixing ratio.
Shown in the table.

第1表は本発明除草剤組成物がシンメスリン及びブロモ
ブチドの単独処理に比べて著しいタイヌビエの除草効果
をもち、極めて大きな相乗効果があることを示している
Table 1 shows that the herbicidal composition of the present invention has a remarkable herbicidal effect on Japanese millet compared to the single treatment of synmethrin and bromobutide, and has an extremely large synergistic effect.

また、各混合比率の除草剤組成物による処理の結果から
、タイヌビエ80%生育抑制を達成した諏草剤組成物中
の各成分の処理量(g/ヘクタール5を混合比率毎にプ
ロットした結果、第1図の等効果曲線が得られた。ブロ
モブチドはタイヌビエに対して殆んど防除効果がないの
で、理論的にはブロモブチドの処理量を増加しても、シ
ンメスリン処理量は変化せず、従って第1図の点線が理
論等効果曲線であるから、これに比べて本発明の除草剤
組成物は、ブロモブチドの添加によってシンメスリンの
使用量が大巾に減少できることがわかる。
In addition, from the results of treatment with herbicide compositions at various mixing ratios, the treatment amount (g/ha5) of each component in the herbicide composition that achieved 80% growth inhibition of Japanese millet was plotted for each mixing ratio. The iso-effect curve shown in Figure 1 was obtained.Since bromobutide has almost no control effect on Japanese millet, theoretically even if the amount of bromobutide treated increases, the amount of synmethrin treated will not change. Since the dotted line in FIG. 1 is a theoretical iso-effect curve, it can be seen that in comparison with this, in the herbicidal composition of the present invention, the amount of synmethrin used can be significantly reduced by adding bromobutide.

試験例2 (シンメスリンとブロモブチドの相乗的除草効果及び水
稲に対する薬害) [試験方法] 面ml/10,000アールのポットにタイヌビエのあ
らかじめ催芽せしめた種子10粒づつを深さ5mm1:
:播種した。
Test Example 2 (Synergistic herbicidal effect of synmethrin and bromobutide and phytotoxicity on paddy rice) [Test method] Ten pre-germinated seeds of Japanese millet were placed in a pot with a surface area of ml/10,000 are at a depth of 5 mm.
: Sown.

その3日後2.5葉に生育した水稲の苗を3本1株とし
、面積1/10,000アールのポット当り3株を深さ
1.0cmに移植した。水深はいずれも3cmに保・)
だ。
Three days later, three paddy rice seedlings that had grown to 2.5 leaves were transplanted to a depth of 1.0 cm per pot with an area of 1/10,000 are. The water depth is kept at 3cm in both cases.)
is.

10日後、タイヌビエが2.0葉期に達し、水稲は移植
後7日に達した時に、試験例1と同様にして調製した除
草組成物溶液にて処理した。
Ten days later, when the Japanese millet reached the 2.0 leaf stage and the paddy rice reached 7 days after transplanting, it was treated with a herbicidal composition solution prepared in the same manner as in Test Example 1.

但し基本旭理量及び混合比率は次の通りである。However, the basic amount and mixing ratio are as follows.

希釈倍率は試験例1と同一の5濃度を用い、試験は3反
復で行われた。
The same 5 concentrations as in Test Example 1 were used as the dilution ratio, and the test was repeated three times.

必要に応じて肉眼観察を行い、薬剤処理2週間後に、タ
イヌビエ、水稲の生体重を測定した。各混合比率での処
理について、5濃度、3反復の生体重の平均値を第2表
に示した。
Macroscopic observation was carried out as necessary, and fresh weights of Japanese millet and paddy rice were measured two weeks after the drug treatment. Table 2 shows the average live weight of 3 replicates at 5 concentrations for each treatment at each mixing ratio.

第2表の結果から、単独処理では殆んどタイヌビエに対
して効果のないブロモブチドが、シンメスリンとの混合
組成物においては有効に作用しており、しかも本発明の
除草剤組成物はシンメスリン及びブロモブチド単独処理
と同じく、水稲に対して極めて安全性の高い除草剤組成
物であることがわかる。
From the results in Table 2, it is clear that bromobutide, which is hardly effective against Japanese millet when treated alone, is effective in a mixed composition with synmethrin, and that the herbicide composition of the present invention is effective against synmethrin and bromobutide. It can be seen that the herbicide composition is extremely safe for paddy rice, as is the case with the single treatment.

試験例3 (ホタルイに対するシンメスリンとブロモブチドの相乗
的除草効果について) [試験方法1 面積115,000アールのワグナ−ポットに約400
粒のホタルイの種子を土壌表面に播種し、約3mmの厚
さで覆土した。
Test Example 3 (About the synergistic herbicidal effect of synmethrin and bromobutide on firefly) [Test method 1 Approximately 400 herbicides were placed in a Wagner pot with an area of 115,000 are.
Granular firefly seeds were sown on the soil surface and covered with soil to a thickness of about 3 mm.

1日後に2.5葉に生育した水稲の苗を3本I株として
、面1t15,000アールのポット当り3株を深さ1
.0cmに移植した。
Three paddy rice seedlings that grew to 2.5 leaves after 1 day were designated as I plants, and 3 plants per pot with a surface of 1 t and 15,000 are were placed at a depth of 1.
.. It was transplanted at 0 cm.

水深を常時3cmに保ち、ホタルイの1.0〜1.5葉
期及び水稲の移植6日後と9日後にそれぞれ試験例1と
同様にして調製した除草剤組成物溶液により薬剤処理し
た。但し処理量及び混合比率は下記の6種とし、濃度は
1種のみで試験は各調査は必要に応じて肉眼観察を行な
い、水稲は7日ごとに草丈、茎数を測定した。最終調査
は処理21日後にホタルイ及び水稲の生体重(9)を測
定した。各混合比率での処理による4反復の平均生体重
(9)を無処理区の生体重(9)に対する比率で第3表
に示した。
The water depth was always maintained at 3 cm, and the plants were treated with a herbicide composition solution prepared in the same manner as in Test Example 1 at the 1.0 to 1.5 leaf stage of firefly and 6 and 9 days after transplanting paddy rice. However, the treatment amount and mixing ratio were the following six types, and the concentration was only one type.In each test, visual observation was performed as necessary, and the plant height and number of stems of rice were measured every 7 days. In the final investigation, fresh weights (9) of firefly and paddy rice were measured 21 days after treatment. Table 3 shows the average fresh weight (9) of four replicates of treatment at each mixing ratio as a ratio to the fresh weight (9) of the untreated group.

第3表の結果から本発明の除草剤組成物はホタルイに対
しても、相乗的除草効果を有し、一方水稲に対する薬害
は殆んどなく、極めて安全性の高い除草剤組成物である
ことが示されている。
From the results in Table 3, the herbicide composition of the present invention has a synergistic herbicidal effect on firefly as well, while causing almost no chemical damage to paddy rice, indicating that it is an extremely safe herbicide composition. It is shown.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図はタイヌビエの80%生育抑制におけるシンメス
リン及びブロモブチド混合処理による等効果曲線である
。 特許出願人 シェル化学株式会社
FIG. 1 is an iso-effect curve of the mixed treatment of synmethrin and bromobutide in inhibiting the growth of Japanese millet by 80%. Patent applicant Shell Chemical Co., Ltd.

Claims (1)

【特許請求の範囲】 1、A、(±)−2−エキソ−(2−メチルベンジルオ
キシ)−1−メチル−4−イソプロピル−7−オキサビ
シクロ[2.2.1]ヘプタン及び B、(RS)−2−ブロモ−N−(α,α−ジメチルベ
ンジル)−3,3−ジメチルブチルアミド を有効成分として含有することを特徴とする除草剤組成
物。
[Scope of Claims] 1, A, (±)-2-exo-(2-methylbenzyloxy)-1-methyl-4-isopropyl-7-oxabicyclo[2.2.1]heptane and B, ( RS)-2-bromo-N-(α,α-dimethylbenzyl)-3,3-dimethylbutyramide as an active ingredient.
JP6731688A 1988-03-23 1988-03-23 Herbicide composition Expired - Lifetime JP2549142B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6731688A JP2549142B2 (en) 1988-03-23 1988-03-23 Herbicide composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6731688A JP2549142B2 (en) 1988-03-23 1988-03-23 Herbicide composition

Publications (2)

Publication Number Publication Date
JPH01242506A true JPH01242506A (en) 1989-09-27
JP2549142B2 JP2549142B2 (en) 1996-10-30

Family

ID=13341494

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6731688A Expired - Lifetime JP2549142B2 (en) 1988-03-23 1988-03-23 Herbicide composition

Country Status (1)

Country Link
JP (1) JP2549142B2 (en)

Also Published As

Publication number Publication date
JP2549142B2 (en) 1996-10-30

Similar Documents

Publication Publication Date Title
KR100276932B1 (en) Herbicide composition
US2423284A (en) Insecticides
KR20080014459A (en) Synergistic herbicidal compositions comprising metamifop
JP2002524396A (en) Sterilizing mixture containing R-metalaxyl
JPH01213202A (en) Herbicide composition
JPH01242506A (en) Herbicide composition
JPH03227904A (en) Agricultural and horticultural soil disease controlling agent
JP2509604B2 (en) Composition for agricultural sterilization and plant growth control
CN114982765B (en) Pesticide composition and preparation and application thereof
JPS6045503A (en) Herbicide
JP2807503B2 (en) Herbicidal effect enhancer and herbicidal granules containing water applied thereto
JPS63179806A (en) Herbicide composition
KR100449464B1 (en) Prochloraz Mixtures
JPH03284601A (en) Bactericidal composition for agriculture and horticulture
JPH05186306A (en) Herbicide composition
JPS5843905A (en) Fungicide and insecticide composition for rice crop
JPS6366104A (en) Agent for reducing injury from salt and phytotoxicity of crop
JPH04173702A (en) Mitigative agent for nitrate-nitrogen content of plant and mitigating method using the same
JPS61233605A (en) Herbicide composition
JPH0446921B2 (en)
JPS5827766B2 (en) Tansuiden Youjiyosouzai
JPH03123709A (en) Herbicide composition
JPH01113303A (en) Yield increasing agent for rice plant
JPS63287704A (en) Herbicidal composition for paddy field
JPH0327521B2 (en)