JPS63104904A - Herbicide composition - Google Patents

Herbicide composition

Info

Publication number
JPS63104904A
JPS63104904A JP61250158A JP25015886A JPS63104904A JP S63104904 A JPS63104904 A JP S63104904A JP 61250158 A JP61250158 A JP 61250158A JP 25015886 A JP25015886 A JP 25015886A JP S63104904 A JPS63104904 A JP S63104904A
Authority
JP
Japan
Prior art keywords
active ingredients
formula
bialaphos
compound
salt
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
JP61250158A
Other languages
Japanese (ja)
Inventor
Masayuki Takase
雅之 高瀬
Akira Yoshida
亮 吉田
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical Co 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP61250158A priority Critical patent/JPS63104904A/en
Priority to CA000524535A priority patent/CA1277152C/en
Priority to EP19860117038 priority patent/EP0232504B1/en
Priority to DE8686117038T priority patent/DE3673984D1/en
Priority to AU66349/86A priority patent/AU585678B2/en
Priority to BR8606057A priority patent/BR8606057A/en
Publication of JPS63104904A publication Critical patent/JPS63104904A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To produce a herbicidal composition capable of extremely controlling a wide range of weeds growing in agricultural lands and nonagricultural lands, showing wider herbicidal spectrum with a small amount by synergistic action compared with separative use of each component comprising a specific compound, bialaphos, etc., as active ingredients. CONSTITUTION:A herbicidal composition comprising 3-chloro-2-(4-2-fluoro-5- propargyloxyphenyl)-4,5,6,7-tetrah-ydro-2H-indazole shown by formula I and bialaphos [=(2-amino-4-methylphosphinobutyryl)alanylalanine) shown by formula II or a salt thereof or DL-homoalanin-4-yl(methyl)phosphinic acid shown by the formula II or a salt thereof as active ingredients. The blending ratio is 0.2-100pts.wt. compound shown by formula II, etc., based on 1pt.wt. compound shown by containing I and the active ingredients are mixed with a carrier and an auxiliary, prepared into emulsion, wettable powder, etc., and applied. An application amount is 1-100g/a sum of the active ingredients.

Description

【発明の詳細な説明】 本発明は、8−クロロ−2−(4−クロロ−2−フルオ
ロ−5−プロパルギルオキシフェニル)−4,5,6,
7−テトラヒドロ−2H−インダゾール(以下、化合物
[1)と記す。)と、(2−アミノ−4−メチルホスフ
ィノブチリル)アラニルアラニン若しくはその塩(以下
、ビアラホスと記す。)またはDL−ホモアラニン−4
−イル(メチル)ホスフィン酸若しくはその塩(以下、
グルホシネートと記す。)とを有効成分として含有する
除草組成物(以下、本発明組成物と記す。)に関するも
のである。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides 8-chloro-2-(4-chloro-2-fluoro-5-propargyloxyphenyl)-4,5,6,
7-tetrahydro-2H-indazole (hereinafter referred to as compound [1). ) and (2-amino-4-methylphosphinobutyryl)alanylalanine or its salt (hereinafter referred to as bialaphos) or DL-homoalanine-4
-yl(methyl)phosphinic acid or its salt (hereinafter referred to as
It is written as glufosinate. ) as an active ingredient (hereinafter referred to as the composition of the present invention).

現在、農耕地あるいは非農耕地用として、数多くの除草
剤が使用されているが、防除の対象となる雑草は、種類
も多く、発生も長期にわたるため、より除草効果が趙く
、幅広い殺草スペクトラムを持った除草剤の開発が望ま
れている。
Currently, a large number of herbicides are used for agricultural and non-agricultural land, but since there are many types of weeds to control and the growth period is long, the herbicides are more effective and can be used to control a wide range of weeds. The development of herbicides with a spectrum is desired.

本発明首等は、このような目的に合致する除雄剤を開発
すべ(種々検討した結果、化合物(4)と、ビアラホス
またはグルホシネートとを有効成分として含有する本発
明組成物が、農耕地あるいは非農耕地に発生する広範囲
の雑草を防除し、しかもその除草効果はそれらと単独で
用いる場合に比較して、相乗的に増大し、低薬量で施用
でき、かつ殺草スペクトルの拡大を見い出し、本発明を
完成した。
The inventors of the present invention have developed an emasculating agent that meets these objectives (as a result of various studies, it has been found that the composition of the present invention containing the compound (4) and bialaphos or glufosinate as active ingredients is suitable for agricultural land or It has been discovered that it controls a wide range of weeds that occur in non-agricultural land, has a synergistic herbicidal effect compared to when used alone, can be applied at low dosages, and has an expanded herbicidal spectrum. , completed the invention.

本発明組成物によって防除できる雑草としては、ソバカ
ズラ、サナエタデ、ギシギシ、スベリヒュ、ハコベ、シ
ロザ、アオゲイトウ、ダイコン、ノハラガラシ、ナズナ
、アメリカツノクサネム、エビスグサ、イチビ、アメリ
カキンゴジカ、フィールドパンジー、ヤエムグラ、アメ
リカアサガオ、マルパアサガオ、セイヨウヒルガオ、ヒ
メオドリコソウ、ホトケノザ、シロバナナ1ウセンアサ
ガオ、イヌホオズキ、オオイヌノフグリ、オナモミ、ヒ
マワリ、イヌカミツレ、コーンマリーゴールド、ヨモギ
等の広葉雑草、ヒエ、イヌビエ、エノコログサ、メヒシ
バ、スズメノカタビラ、ノスズメノテッポウ、エンバク
、カラスムギ、セイバンモロコシ、シバムギ、ウマノチ
ャヒキ、ギ、ウギシバ等のイネ科雑草およびツユクサ等
のツユクサ科雑草、コゴメガヤツリ、ハマスゲ等のカヤ
ツリグサ科雑草等があげられる。
Weeds that can be controlled by the composition of the present invention include: freckles, Japanese knotweed, Japanese grass, purslane, chickweed, whiteweed, Japanese radish, Japanese radish, Japanese radish, shepherd's purse, American hornwort, Ebisu grass, Japanese commonweed, American golden deer, field pansy, Japanese violet, and American morning glory. , broad-leaved weeds such as Marupa morning glory, St. bindweed, Hemlockweed, Hotokenoza, White banana 1 Hemlock, Physalis occidentalis, Psyllium japonica, Japanese fir tree, sunflower, Japanese chamomile, corn marigold, mugwort, etc., barnyard grass, Japanese millet, foxtail grass, Japanese grasshopper, Psyllium annuus, Prunus japonicum, Oat Examples include weeds of the Poaceae family, such as oats, Seiban sorghum, grasshoppers, Japanese sorghum, Cyperaceae, Cyperaceae weeds such as Cyperaceae, Cyperaceae such as Cyperus japonica, and Cyperaceae.

化合物〔■〕(特開昭59−84872号公報)は除草
効力を有し、またビアラホス〔竹松哲夫看、除草剤研究
総覧第611頁(1982年〕等参照〕及びグルホシネ
ー) (C,R,Worthing。
Compound [■] (Japanese Unexamined Patent Publication No. 59-84872) has a herbicidal effect, and also has bialaphos (see Tetsuo Takematsu, Herbicide Research Directory, p. 611 (1982), etc.) and glufosine) (C,R, Worthing.

The Pe5ticide Manual第7版第8
02頁(1988年)等参照〕は、除草剤として知られ
ている。
The Pe5ticide Manual 7th Edition No. 8
02 (1988) etc.] is known as a herbicide.

本発明組成物の有効成分である化合物[1)と、ビアラ
ホスまたはグルホシネートとの混合割合は比較的広い範
囲に変えることができるが、通常は化合物(1)1.[
1部に対してビアラホスまたはグルホシネートは0.2
〜100東ffi部であり、好ましくは0.4〜70!
!1部である。
The mixing ratio of compound [1), which is an active ingredient of the composition of the present invention, and bialaphos or glufosinate can be varied within a relatively wide range, but usually compound (1) 1. [
Bialaphos or glufosinate is 0.2 to 1 part
~100 east ffi part, preferably 0.4~70!
! This is part 1.

化合物〔I〕、ビアラホス及びグルホシネートの化学構
造式を第1表に示す。
The chemical structural formulas of Compound [I], bialaphos and glufosinate are shown in Table 1.

第  1  表 なお、(2−アミノ−4−メチルホスフィノブチリル)
アラニルアラニンの塩としては、ナトリウム塩等が、ま
たDL−ホモアラニン−4−イル(メチル)ホスフィン
酸の塩としては、アンモニウム塩等があげられる。
Table 1 In addition, (2-amino-4-methylphosphinobutyryl)
Examples of salts of alanylalanine include sodium salts, and examples of salts of DL-homoalanin-4-yl(methyl)phosphinic acid include ammonium salts.

本発明組成物を除草剤として用いる場合は、通常固体担
体、液体担体、界面活性剤、その他の製剤用補助剤と混
合して、乳剤、水和剤、懸濁剤等に製剤する。
When the composition of the present invention is used as a herbicide, it is usually mixed with a solid carrier, a liquid carrier, a surfactant, and other formulation auxiliaries to formulate an emulsion, wettable powder, suspension, or the like.

これらの製剤には有効成分として本発明化合物を、重鐵
比で1〜90%、好ましくは2〜80チ含有する。
These preparations contain the compound of the present invention as an active ingredient in a weight ratio of 1 to 90%, preferably 2 to 80%.

固体担体としては、カオリンクレー、アッタパルジャイ
トクレー、ベントナイト、酸性白土、パイロフィライト
、タルク、珪藻土、方解石、クルミ粉、尿素、硫酸アン
モニウム、合成含水酸化理系等の微粉末あるいは粒状物
があげられ、液体担体としては、キシレン、メチルナフ
タレン等の芳香族炭化水素類、イソプロパツール、エチ
レングリコール、セロソルブ等のアルコール類、アセト
ン、シクロヘキサノン、イソホロン等のケトン類、大豆
油、綿実油等の植物油、ジメチルスルホキシド、アセト
ニトリル、水等があげられる。
Examples of solid carriers include fine powders or granules such as kaolin clay, attapulgite clay, bentonite, acid clay, pyrophyllite, talc, diatomaceous earth, calcite, walnut powder, urea, ammonium sulfate, and synthetic hydrous oxidation systems. Liquid carriers include aromatic hydrocarbons such as xylene and methylnaphthalene, alcohols such as isopropanol, ethylene glycol, and cellosolve, ketones such as acetone, cyclohexanone, and isophorone, vegetable oils such as soybean oil and cottonseed oil, and dimethyl sulfoxide. , acetonitrile, water, etc.

乳化、分散、湿層等のために用いられる界面活性剤とし
ては、アルキル硫酸エステル塩、アルキルアリールスル
ホン酸塩、ジアルキルスルホコハク酸塩、ポリオキシエ
チレンアルキルアリールエーテルリン酸エステル塩等の
陰イオン界面活性剤、ポリオキシエチレンアルキルエー
テル、ポリオキシエチレンアルキルアリールエーテル、
ポリオキシエチレンポリオキシプロピレンブロックコポ
リマー、ソルビタン脂肪酸エステル、ポリオキシエチレ
ンソルビタン脂肪酸エステル等の非イオン界面活性剤等
があげられる。その他の製剤用補助剤としては、リグニ
ンスルホン酸塩、アルギン酸塩、ポリビニルアルコール
、アラビアガム、CMC(カルボキシメチルセルロース
)、PAP(酸性リン酸イソプロピル)等があげられる
Surfactants used for emulsification, dispersion, wetting layers, etc. include anionic surfactants such as alkyl sulfate salts, alkylaryl sulfonates, dialkyl sulfosuccinates, and polyoxyethylene alkylaryl ether phosphate salts. agent, polyoxyethylene alkyl ether, polyoxyethylene alkylaryl ether,
Examples include nonionic surfactants such as polyoxyethylene polyoxypropylene block copolymers, sorbitan fatty acid esters, and polyoxyethylene sorbitan fatty acid esters. Other formulation adjuvants include lignin sulfonate, alginate, polyvinyl alcohol, gum arabic, CMC (carboxymethyl cellulose), PAP (isopropyl acid phosphate), and the like.

次に製剤例を示す。なお1部はM承部を示す。Examples of formulations are shown below. Note that part 1 shows the M-receiving part.

製剤例1 化合物(I) 25部、ビアラホス25部、リグニンス
ルホン酸カルシウム8部、ラウリル硫酸ナトリウム2部
および合成含水酸化珪素45部をよく粉砕混合して水和
剤を得る。
Formulation Example 1 25 parts of compound (I), 25 parts of bialaphos, 8 parts of calcium lignosulfonate, 2 parts of sodium lauryl sulfate, and 45 parts of synthetic hydrous silicon oxide are thoroughly ground and mixed to obtain a wettable powder.

製剤例2 化合物(1) 10 =6s  ビアラホスまたはグル
ホシネート15m5ポリオキシエチレンソルビタンモノ
オレエート8部、CMCa部、水69部を混合し、粒度
が5ミクロン以下になるまで湿式粉砕して懸濁剤を得る
Formulation Example 2 Compound (1) 10 = 6s Bialaphos or Glufosinate 15m5 8 parts of polyoxyethylene sorbitan monooleate, CMCa part, and 69 parts of water were mixed and wet-pulverized until the particle size became 5 microns or less to form a suspension. obtain.

製剤例8 化合物(1) 25部、グリホラネート25部、リグニ
ンスルホン酸カルシウム8部、ラウリル硫酸ナトリウム
2部および合成含水酸化珪素45部をよく粉砕混合して
水和剤を得る。
Formulation Example 8 25 parts of Compound (1), 25 parts of glyfolanate, 8 parts of calcium lignosulfonate, 2 parts of sodium lauryl sulfate, and 45 parts of synthetic hydrous silicon oxide are thoroughly ground and mixed to obtain a wettable powder.

このようにして製剤された本発明組成物は、雑草の出芽
後に茎葉処理する。
The composition of the present invention prepared in this manner is applied to the foliage of weeds after they emerge.

また、他の除草剤と混合して用いることにより、除草効
力の増強を期待できる。さらに、殺虫剤、殺ダニ剤、殺
線虫剤、殺菌剤、植物生長調節剤等と混合して用いるこ
ともできる。
Furthermore, by mixing it with other herbicides, it can be expected to increase the herbicidal efficacy. Furthermore, it can also be used in combination with insecticides, acaricides, nematicides, fungicides, plant growth regulators, and the like.

なお、本発明組成物は、畑地、休耕地、果樹園、牧草地
、芝生地、森林あるいは非農耕地等の除草剤として用い
ることができる。
The composition of the present invention can be used as a herbicide for fields, fallow fields, orchards, pastures, lawns, forests, non-agricultural lands, and the like.

本発明組成物の施用量は有効成分の混合比、製剤形態、
対象雑草の種類、気象条件等により異なるが、通常1ア
ールあたりの有効成分の合計量が12〜100F、好ま
しくは22〜602であり、乳剤、水和剤、懸濁剤等は
、通常その所定量を1アールあたり1リツトル〜10リ
ツトルの(必要ならば、展着剤等の補助剤を添加した)
水で希釈して処理する。
The application amount of the composition of the present invention depends on the mixing ratio of the active ingredients, the formulation form,
Although it varies depending on the type of target weed, weather conditions, etc., the total amount of active ingredients per are is usually 12 to 100 F, preferably 22 to 60 F, and emulsions, wettable powders, suspensions, etc. The amount is 1 liter to 10 liters per are (if necessary, auxiliary agents such as a spreading agent are added)
Dilute with water and process.

展着剤としては、前記の界面活性剤のほか、ポリオキシ
エチレン樹脂酸(エステル)、リグニンスルホン酸塩、
アビエチン酸塩、ジナフチルメタンジスルホン酸塩、パ
ラフィン等があげられる。
In addition to the above-mentioned surfactants, the spreading agents include polyoxyethylene resin acid (ester), lignin sulfonate,
Examples include abietate, dinaphthylmethane disulfonate, and paraffin.

次に試験例をあげて本発明組成物の除草効力を具体的に
示す。
Next, test examples will be given to specifically demonstrate the herbicidal efficacy of the composition of the present invention.

なお除草効力は調査時に枯れ残った供試植物の地上部の
生産量をはかり、次式により算出した生育抑制率←)で
示す。
The herbicidal efficacy is expressed as the growth suppression rate ←) calculated by the following formula by measuring the production of the above-ground parts of the test plants that remained dead at the time of the survey.

生育抑制率(に)− 試験例1 畑地茎葉処理試験 内径16cm1.深さ19a1のワグネルホ0ットに畑
地土壌を詰め、スズメノカタビラまたはスズメノカタビ
ラを1僑櫨し、85日間育成した。その後、製剤例1あ
るいは製剤例8に準じて供試物を水和剤にし、その所定
量を、展着剤を含む1アールあたり5リツトル相当の水
で希釈し、小型噴霧器で植物体の上方から茎葉部全面に
均一に処理した。このときスズメノカタビラの生育状況
は、6〜7葉期で、草丈20〜80コ、またスズメノカ
タビラの生育状況は5〜7葉期で、草丈lO〜15cm
であった。処理20日後に除草効力を調査した。
Growth inhibition rate (in) - Test Example 1 Field soil stem and leaf treatment test Inner diameter 16cm1. A Wagner hole with a depth of 19 a1 was filled with upland soil, and one sycamore or sycamore was planted in a box and grown for 85 days. Thereafter, make the test material into a hydrating powder according to Formulation Example 1 or Formulation Example 8, dilute the specified amount with water containing a spreading agent equivalent to 5 liters per are, and use a small sprayer to spray it onto the top of the plant body. The whole surface of the stems and leaves was treated uniformly. At this time, the growth status of Sparrow vulgare is in the 6-7 leaf stage, and the plant height is 20-80 cm.
Met. The herbicidal efficacy was investigated 20 days after the treatment.

その結果を第2表および第8表に示す。なお、本試験は
、全期間を通して温室で行なった。
The results are shown in Tables 2 and 8. This test was conducted in a greenhouse throughout the entire period.

第  2  表 第  8  表 第2表および第8表の結果を等効果線法〔深見順−1上
杉康彦、石塚皓造、冨沢長次部編農薬実験法第3巻除草
剤編第1版第109〜ILL頁(1981年)ソフトサ
イエンス社発行参照〕により作図した。その結果を図1
および図2に示す。該図より、禾発明組成物が相乗効果
を有することが明らかである。
Tables 2 and 8 The results of Tables 2 and 8 were calculated using the isoeffect line method [Fukami order - 1 Yasuhiko Uesugi, Kozo Ishizuka, Choji Tomizawa (eds.) Pesticide Experimental Methods Volume 3 Herbicides Edition 1st Edition 109-ILL pages (1981) published by Soft Science Company]. The results are shown in Figure 1.
and shown in FIG. From the figure, it is clear that the composition of the invention has a synergistic effect.

試験例2 畑地茎葉処理スペクトラム試験面積aax2
ac4、深さIIcIIのバットに畑地土壌を詰め、イ
ヌビエ、エノコログサ、メヒシバ、マルパアサガオ、イ
チビ、エビスグサ、アメリカツノクサネム、アメリカキ
ンゴジカ、イヌホオズキ、オナモミ、ヒマワリ、シロザ
、アオゲイトウを播種し、セイバンモロコシの根茎を移
植し、85日間育成した。
Test example 2 Field soil stem leaf treatment spectrum test area aax2
Pack field soil into a vat of ac4, depth IIcII, and sow goldenberry, foxtail grass, blackberry grass, malpa morning glory, Japanese grasshopper, yellowtail grass, American hornwort, American golden deer, Japanese physalis, Japanese fir tree, sunflower, white locust, and blue sorghum. The rhizomes were transplanted and grown for 85 days.

その後、製剤例1に準じて供試物を水和剤にし、その所
定量を、展着剤を含む1アールあたり5リツトル相当の
水で希釈し、小型噴霧器で植物体の上方から茎葉部全面
に均一に処理した。このとき雑草および作物の生育状況
は草種により異なるが、8〜8葉期で、草丈は5〜60
C!+であっtこ。処理28日後に除草効力を調査した
。その結果を第4表に示す。
Thereafter, the sample was made into a hydrating powder according to Formulation Example 1, a predetermined amount of it was diluted with water equivalent to 5 liters per are including a spreading agent, and a small sprayer was applied from above the plant body to the whole surface of the stems and leaves. was uniformly processed. At this time, the growth conditions of weeds and crops vary depending on the grass species, but the 8-8 leaf stage and the plant height are 5-60 cm.
C! +de attko. Herbicidal efficacy was investigated 28 days after treatment. The results are shown in Table 4.

なお、本試験は、全期間を通して温室で行なった。This test was conducted in a greenhouse throughout the entire period.

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

図1および図2は、それぞれ試験例1中の第2表および
第8表のスズメノカタビラおよびスズメノカタビラに対
する除草効力を基に等効果線法により作図したものであ
る。 縦軸はビアラホスまたはグルホシネートの薬m(9/a
)を、横軸は化合物[1]の薬!ICP/a)をそれぞ
れ表わす。また、破線は相加的効果の線を、実線は生育
抑制率90%の等効果線をそれぞれ表わす。 0      0.5     1.0     1.
5化合物CI)の有効成分量(r/a )図1
FIGS. 1 and 2 are plotted using the isoeffect line method based on the herbicidal efficacy against sycamore and sycamore in Tables 2 and 8 of Test Example 1, respectively. The vertical axis is bialafos or glufosinate drug m (9/a
), and the horizontal axis is the drug of compound [1]! ICP/a) respectively. Moreover, the broken line represents the line of additive effect, and the solid line represents the line of equal effect with a growth inhibition rate of 90%. 0 0.5 1.0 1.
5 Compound CI) active ingredient amount (r/a) Figure 1

Claims (1)

【特許請求の範囲】[Claims] 3−クロロ−2−(4−クロロ−2−フルオロ−5−プ
ロパルギルオキシフェニル)−4,5,6,7−テトラ
ヒドロ−2H−インダゾールと、(2−アミノ−4−メ
チルホスフィノブチリル)アラニルアラニン若しくはそ
の塩またはDL−ホモアラニン−4−イル(メチル)ホ
スフィン酸若しくはその塩とを有効成分として含有する
ことを特徴とする除草組成物。
3-chloro-2-(4-chloro-2-fluoro-5-propargyloxyphenyl)-4,5,6,7-tetrahydro-2H-indazole and (2-amino-4-methylphosphinobutyryl) 1. A herbicidal composition comprising alanylalanine or a salt thereof, or DL-homoalanin-4-yl(methyl)phosphinic acid or a salt thereof as an active ingredient.
JP61250158A 1985-12-10 1986-10-20 Herbicide composition Pending JPS63104904A (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
JP61250158A JPS63104904A (en) 1986-10-20 1986-10-20 Herbicide composition
CA000524535A CA1277152C (en) 1985-12-10 1986-12-04 Herbicidal compositions
EP19860117038 EP0232504B1 (en) 1985-12-10 1986-12-08 Herbicidal composition
DE8686117038T DE3673984D1 (en) 1985-12-10 1986-12-08 HERBICIDAL COMPOSITION.
AU66349/86A AU585678B2 (en) 1985-12-10 1986-12-09 Herbicidal compositions
BR8606057A BR8606057A (en) 1985-12-10 1986-12-09 HERBICIDE COMPOSITION AND PROCESS TO CONTROL WEEDS

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61250158A JPS63104904A (en) 1986-10-20 1986-10-20 Herbicide composition

Publications (1)

Publication Number Publication Date
JPS63104904A true JPS63104904A (en) 1988-05-10

Family

ID=17203685

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61250158A Pending JPS63104904A (en) 1985-12-10 1986-10-20 Herbicide composition

Country Status (1)

Country Link
JP (1) JPS63104904A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008031075A (en) * 2006-07-28 2008-02-14 Bayer Cropscience Kk Method for selectively controlling ipomoeas

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008031075A (en) * 2006-07-28 2008-02-14 Bayer Cropscience Kk Method for selectively controlling ipomoeas

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