JPH04275201A - Herbicide composition - Google Patents

Herbicide composition

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Publication number
JPH04275201A
JPH04275201A JP5774091A JP5774091A JPH04275201A JP H04275201 A JPH04275201 A JP H04275201A JP 5774091 A JP5774091 A JP 5774091A JP 5774091 A JP5774091 A JP 5774091A JP H04275201 A JPH04275201 A JP H04275201A
Authority
JP
Japan
Prior art keywords
mcp
weight
parts
composition
acid
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
JP5774091A
Other languages
Japanese (ja)
Other versions
JP2974806B2 (en
Inventor
Masaru Yokoyama
優 横山
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.)
Kumiai Chemical Industry Co Ltd
Original Assignee
Kumiai Chemical Industry 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 Kumiai Chemical Industry Co Ltd filed Critical Kumiai Chemical Industry Co Ltd
Priority to JP5774091A priority Critical patent/JP2974806B2/en
Publication of JPH04275201A publication Critical patent/JPH04275201A/en
Application granted granted Critical
Publication of JP2974806B2 publication Critical patent/JP2974806B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To provide the title composition capable of selectively, significantly reducing the chemical injuries on barley, wheat, etc., and controlling a wide range of weeds, comprising as active ingredients a dispymidinyloxybenzoic acid derivative and 2,4-D or MCP. CONSTITUTION:The objective composition comprising as active ingradients (A) a compound of the fomula [R is H, alkali metal, alkaline earth metal, ammonium ion, ogranoammonium ion, CH2OCOC4H9-t or CH(CH3)COOC2H5] and (B) a compound selected from 2,4-dichlorophenoxyacetic acid (2,4-D), 2- methyl-4-chlorophenoxyacetic acid (MCP), their salts and their esters at a level of pref. 2-50 pts.wt. (for 2,4-D) or 4-100 pts.wt. (for MCP) per pt.wt. of the component A. The composition has outstanding herbicidal effects on both annual and perennial weeds.

Description

【発明の詳細な説明】[Detailed description of the invention]

【0001】0001

【産業上の利用分野】本発明は除草剤組成物に関するも
のであり、さらに詳しくは一年生雑草及び多年生雑草に
対して卓越した除草効果を示すと共に、作物に対する安
全性が顕著に改善された除草剤組成物に関するものであ
る。
[Field of Industrial Application] The present invention relates to a herbicide composition, and more particularly to a herbicide that exhibits excellent herbicidal effects against annual and perennial weeds and has significantly improved safety for crops. The present invention relates to a composition.

【0002】0002

【従来の技術】本発明の除草剤組成物の一方の有効成分
であるビスピリミジニルオキシ安息香酸誘導体が除草活
性を有することは特開平1−250365号公報あるい
は特願平2−220616号明細書に記載されている。 また、本発明の除草剤組成物の他方の有効成分である2
,4−ジクロルフェノキシ酢酸もしくはその塩またはそ
のエステル(以下、2,4−Dと総称する)、あるいは
2−メチル−4−クロルフェノキシ酢酸もしくはその塩
またはそのエステル(以下、MCPと総称する)は、既
に農耕地あるいは非農耕地用除草剤として広く使用され
ている(農薬要覧1989、451頁)。
[Prior Art] It is disclosed in JP-A No. 1-250365 or Japanese Patent Application No. 2-220616 that the bispyrimidinyloxybenzoic acid derivative, which is one of the active ingredients of the herbicidal composition of the present invention, has herbicidal activity. Are listed. In addition, 2 which is the other active ingredient of the herbicide composition of the present invention
, 4-dichlorophenoxyacetic acid or its salt or its ester (hereinafter collectively referred to as 2,4-D), or 2-methyl-4-chlorophenoxyacetic acid or its salt or its ester (hereinafter collectively referred to as MCP) has already been widely used as a herbicide for agricultural land or non-agricultural land (Pesticide Handbook 1989, p. 451).

【0003】0003

【発明が解決しようとする課題】現在、畑作用除草剤と
して数多くの除草剤が使用されているが、防除の対象と
なる雑草の種類は広範囲に亘っており、また発生も長期
に亘るため、より除草効果が高く幅広い殺草スペクトラ
ムを有し、かつ作物に対しては高い安全性を有する除草
剤が求められている。本発明の除草剤組成物の一方の有
効成分であるビスピリミジニルオキシ安息香酸誘導体は
高い除草効果を示し水稲、小麦等に対する安全性も高い
。しかしながら麦類に使用する場合、耕種条件や小麦の
品種等により薬害を生じる場合があるという問題点を有
している。本発明の目的は、ある種のビスピリミジニル
オキシ安息香酸誘導体と2,4−DもしくはMCPとを
併用することにより、除草効果を維持しつつ、当該ビス
ピリミジニルオキシ安息香酸誘導体に起因する薬害を軽
減し、麦類に安全に使用できる除草剤組成物を提供する
ことにある。
[Problems to be Solved by the Invention] Currently, many herbicides are used as field herbicides, but the types of weeds to be controlled are wide-ranging, and their emergence continues over a long period of time. There is a need for herbicides that have higher herbicidal effects, have a broader herbicidal spectrum, and are highly safe for crops. The bispyrimidinyloxybenzoic acid derivative, which is one of the active ingredients of the herbicidal composition of the present invention, has a high herbicidal effect and is highly safe for paddy rice, wheat, etc. However, when used on wheat, there is a problem in that phytotoxicity may occur depending on the cultivation conditions, wheat variety, etc. The purpose of the present invention is to reduce the phytotoxicity caused by the bispyrimidinyloxybenzoic acid derivative while maintaining the herbicidal effect by using a certain bispyrimidinyloxybenzoic acid derivative in combination with 2,4-D or MCP. The object of the present invention is to provide a herbicide composition that can be safely used on wheat.

【0004】0004

【課題を解決するための手段】本発明の除草剤組成物は
、一般式
[Means for Solving the Problems] The herbicidal composition of the present invention has the general formula

【0005】[0005]

【化2】[Case 2]

【0006】(式中、Rは水素原子、アルカリ金属原子
、アルカリ土類金属原子、アンモニウムイオン、有機ア
ンモニウムイオン、CH2OCOC4H9−t基あるい
はCH(CH3)COOC2H5基を示す。)にて表さ
れるビスピリミジニルオキシ安息香酸誘導体から選ばれ
た1種と2,4−DまたはMCPから選ばれる1種とを
有効成分として含有してなる。
(Wherein, R represents a hydrogen atom, an alkali metal atom, an alkaline earth metal atom, an ammonium ion, an organic ammonium ion, a CH2OCOC4H9-t group or a CH(CH3)COOC2H5 group.) It contains one selected from pyrimidinyloxybenzoic acid derivatives and one selected from 2,4-D or MCP as active ingredients.

【0007】本発明の除草剤組成物の一方の有効成分で
ある前記一般式〔I〕にて表されるビスピリミジニルオ
キシ安息香酸誘導体を例示すれば、表1に記載の通りで
ある。尚、化合物番号は以後の記載において参照される
Examples of the bispyrimidinyloxybenzoic acid derivative represented by the general formula [I], which is one of the active ingredients of the herbicidal composition of the present invention, are shown in Table 1. In addition, the compound number will be referred to in the following description.

【0008】[0008]

【表1】[Table 1]

【0009】また本発明の除草剤組成物の他の有効成分
は、公知の方法で製造できる2,4−ジクロルフェノキ
シ酢酸もしくはその塩またはそのエステル、あるいは2
−メチル−4−クロルフェノキシ酢酸もしくはその塩ま
たはそのエステルである。ここで塩としてはナトリウム
塩、カリウム塩等のアルカリ金属塩、カルシウム塩等の
アルカリ土類金属塩、アミン塩、ジメチルアミン塩等の
無機または有機のアンモニウム塩等があげられる。また
、エステルとしてはエチルエステル、ブチルエステル、
イソプロピルエステル、アリルエステル、イソオクチル
エステル等があげられる。
Other active ingredients of the herbicidal composition of the present invention include 2,4-dichlorophenoxyacetic acid, a salt thereof, or an ester thereof, which can be produced by a known method.
-Methyl-4-chlorophenoxyacetic acid, a salt thereof, or an ester thereof. Examples of the salt include alkali metal salts such as sodium salts and potassium salts, alkaline earth metal salts such as calcium salts, and inorganic or organic ammonium salts such as amine salts and dimethylamine salts. In addition, esters include ethyl ester, butyl ester,
Examples include isopropyl ester, allyl ester, isooctyl ester, and the like.

【0010】本発明の除草剤組成物の2つの有効成分の
混合割合は、それぞれ広い範囲で変えることができるが
、一般式〔I〕にて表される化合物と2,4−Dとを混
合する場合では、前者1重量部に対して後者が1〜10
0重量部、好ましくは2〜50重量部が適当である。 また、一般式〔I〕にて表される化合物とMCPとの混
合割合は、前者1重量部に対して後者1〜200重量部
、好ましくは4〜100重量部が適当である。
Although the mixing ratio of the two active ingredients in the herbicidal composition of the present invention can be varied within a wide range, it is possible to mix the compound represented by the general formula [I] with 2,4-D. In cases where the latter is 1 to 10 parts by weight of the former,
0 parts by weight, preferably 2 to 50 parts by weight are suitable. The appropriate mixing ratio of the compound represented by formula [I] and MCP is 1 to 200 parts by weight, preferably 4 to 100 parts by weight, per 1 part by weight of the former.

【0011】本発明の除草剤組成物は2種類の化合物を
そのまま施用してもよいが、通常は農薬の製剤化に際し
一般的に用いられる担体、界面活性剤、分散剤、補助剤
等を配合して、水和剤、粒剤、乳剤または懸濁剤等の各
種形態に製剤して施用するのが好ましい。
[0011] Although the two types of compounds may be applied as they are to the herbicidal composition of the present invention, carriers, surfactants, dispersants, adjuvants, etc. commonly used in the formulation of agricultural chemicals are usually added. It is preferable to formulate and apply it in various forms such as wettable powders, granules, emulsions, or suspensions.

【0012】製剤化に際して用いられる担体としては、
例えばジークライト、タルク、ベントナイト、クレー、
カオリン、珪藻土、ホワイトカーボン、バーミキュライ
ト、消石灰、珪砂、硫安、尿素等の固体担体、イソプロ
ピルアルコール、キシレン、シクロヘキサノン、メチル
ナフタレン、アセトン、イソホロン、ジメチルスルホキ
シド、アセトニトリル、植物油、水等の液体担体等があ
げられる。
[0012] As carriers used in formulation,
For example, Sieglite, talc, bentonite, clay,
Examples include solid carriers such as kaolin, diatomaceous earth, white carbon, vermiculite, slaked lime, silica sand, ammonium sulfate, and urea, and liquid carriers such as isopropyl alcohol, xylene, cyclohexanone, methylnaphthalene, acetone, isophorone, dimethyl sulfoxide, acetonitrile, vegetable oil, and water. It will be done.

【0013】界面活性剤及び分散剤としては、例えばア
ルコール硫酸エステル塩、アルキルアリールスルホン酸
塩、リグニンスルホン酸塩、ポリオキシエチレングリコ
ールエーテル、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ソルビタンモノアルキレー
ト等があげられる。補助剤としては、例えばカルボキシ
メチルセルロース、ポリエチレングリコール、アラビア
ゴム等があげられる。
[0013] Examples of surfactants and dispersants include alcohol sulfate ester salts, alkylaryl sulfonates, lignin sulfonates, polyoxyethylene glycol ethers, polyoxyethylene alkylaryl ethers, polyoxyethylene sorbitan monoalkylates, etc. can be given. Examples of the adjuvant include carboxymethyl cellulose, polyethylene glycol, and gum arabic.

【0014】本発明の除草剤組成物は、さらに他の除草
剤と混合して使用することによって除草効果の増強も期
待できる。また必要に応じて、殺虫剤、殺菌剤、植物生
長調節剤、肥料等と混合して用いることができる。
[0014] The herbicidal composition of the present invention can be expected to have an enhanced herbicidal effect when used in combination with other herbicides. Further, if necessary, it can be used in combination with an insecticide, a fungicide, a plant growth regulator, a fertilizer, etc.

【0015】本発明の除草剤組成物は、上記により得ら
れた製剤を水等で適当な濃度に希釈して散布するかまた
は直接施用する。本発明の除草剤組成物の施用量は、対
象雑草、作物の種類、気象条件、組成物の製剤形態、有
効成分の混合比、施用方法、施用時期等により異なるが
、有効成分の合計量で1ヘクタール当たり10g〜20
00g、好ましくは2,4−Dとの混用で50〜700
g、MCPとの混用で50〜1300gが適当である。 本発明の除草剤組成物は、麦類での雑草防除に最適であ
るが、他の畑作物あるいは水稲における雑草防除に適用
しても良い。
The herbicidal composition of the present invention is prepared by diluting the above-obtained preparation with water or the like to an appropriate concentration and then spraying or directly applying it. The application amount of the herbicide composition of the present invention varies depending on the target weed, the type of crop, weather conditions, the formulation form of the composition, the mixing ratio of the active ingredients, the method of application, the timing of application, etc. 10g-20 per hectare
00g, preferably 50-700 when mixed with 2,4-D
g, 50 to 1300 g is appropriate when mixed with MCP. The herbicide composition of the present invention is most suitable for weed control in wheat, but may also be applied to weed control in other field crops or paddy rice.

【0016】本発明の除草剤組成物は、作物畑に発生す
るヒエ類、メヒシバ、オヒシバ、エノコログサ、スズメ
ノテッポウ、ノスズメノテッポウ、スズメノカタビラ、
カラスムギ、イタリアンライグラス、ハコベ、ナズナ、
ヤエムグラ、イヌカミツレ、オオイヌノフグリ等のフグ
リ類、スミレ類、オオイヌタデ、アオビユ、シロザ、ア
カザ、イチビ、アメリカキンゴジカ、エビスグサ、ノア
サガオ、オナモミ、コゴメガヤツリ、メリケンニクキビ
、イッチグラス、ウマノチャヒキ、ノハラガラシ、アメ
リカセンダングサ等の一年生雑草及びハマスゲ、ジョン
ソングラス、ギョウギシバ、シバムギ等の多年生雑草の
発生時から生育期まで有効に防除でき、かつ麦類に対す
る薬害が回避しがたい悪条件下で用いても、除草効果を
低下させることなく、麦類に対する薬害のみを顕著に軽
減するという特徴を有するものである。また本発明の除
草剤組成物は、各々の有効成分を単独で用いる場合には
防除が不十分である雑草に対しても有効に防除すること
ができる。
[0016] The herbicide composition of the present invention can be used to control barnyard grasses, Japanese grasshopper, Japanese grasshopper, Japanese foxtail grass, Japanese grasshopper, Japanese grasshopper, Japanese grasshopper, and Japanese grasshopper that occur in crop fields.
Oats, Italian ryegrass, chickweed, shepherd's purse,
Annuals such as pufferfish, violets, Japanese knotweed, Japanese violets, Japanese violet, Japanese staghorn, Japanese redweed, American king deer, Ebisugusa, Noassa glories, Japanese fir, Japanese cypress, American chili grass, witch grass, Japanese chahiki, Japanese grasshopper, American helium, etc. To be able to effectively control weeds and perennial weeds such as porcupine grass, johnson grass, silver grass, and grasshopper from the time of emergence to the growing season, and to reduce the herbicidal effect even when used under adverse conditions where chemical damage to wheat is difficult to avoid. It is characterized by significantly reducing only the chemical damage to wheat. Furthermore, the herbicidal composition of the present invention can effectively control weeds that are insufficiently controlled when each active ingredient is used alone.

【0017】[0017]

【実施例】次に、本発明の除草剤組成物の実施例をあげ
るが、本発明はこの範囲に限定されるものではない。ま
た、2,4−Dはアミン塩、MCPはナトリウム塩を代
表例として示すが、これに限定されるものでなく他の形
態でも同様に実施できる。 実施例1(液剤) 化合物(2)2重量部、2,4−Dアミン塩25重量部
、ポリオキシエチレンラウリルエーテル5重量部及び水
68重量部を均一に撹拌して液剤とする。
[Examples] Next, examples of the herbicidal composition of the present invention will be given, but the present invention is not limited to this scope. In addition, although 2,4-D is an amine salt and MCP is a sodium salt as representative examples, the present invention is not limited to these and other forms can be used in the same manner. Example 1 (Liquid) 2 parts by weight of compound (2), 25 parts by weight of 2,4-D amine salt, 5 parts by weight of polyoxyethylene lauryl ether, and 68 parts by weight of water are uniformly stirred to prepare a liquid.

【0018】実施例2(液剤) 化合物(2)0.5重量部、MCPナトリウム塩12.
5重量部、ポリオキシエチレンノニルフェニルエーテル
5重量部及び水82重量部を均一に溶解して液剤とする
Example 2 (Liquid) 0.5 parts by weight of compound (2), MCP sodium salt 12.
5 parts by weight of polyoxyethylene nonylphenyl ether and 82 parts by weight of water are uniformly dissolved to prepare a liquid agent.

【0019】実施例3(水和剤) 化合物(2)2重量部、2,4−Dアミン塩25重量部
、ジナフチルメタンジスルホン酸ナトリウム2重量部、
リグニンスルホン酸ナトリウム3重量部、ホワイトカー
ボン5重量部及び珪藻土63重量部を均一に混合し粉砕
して水和剤とする。
Example 3 (Wettable powder) 2 parts by weight of compound (2), 25 parts by weight of 2,4-D amine salt, 2 parts by weight of sodium dinaphthylmethane disulfonate,
3 parts by weight of sodium ligninsulfonate, 5 parts by weight of white carbon, and 63 parts by weight of diatomaceous earth are uniformly mixed and ground to obtain a wettable powder.

【0020】実施例4(水和剤) 化合物(2)1重量部、MCPナトリウム塩25重量部
、メチルナフタレンスルホン酸ナトリウムホルマリン縮
合物3重量部、ドデシルベンゼンスルホン酸ナトリウム
2重量部、ホワイトカーボン5重量部及び珪藻土64重
量部を均一に混合し粉砕して水和剤とする。
Example 4 (Wettable powder) 1 part by weight of compound (2), 25 parts by weight of MCP sodium salt, 3 parts by weight of sodium methylnaphthalenesulfonate formalin condensate, 2 parts by weight of sodium dodecylbenzenesulfonate, White Carbon 5 Parts by weight and 64 parts by weight of diatomaceous earth are uniformly mixed and ground to obtain a wettable powder.

【0021】次に、本発明除草剤組成物の奏する効果を
試験例をあげて具体的に説明する。 試験例1(畑作茎葉処理) 土壌を充填した各ポット(800cm2)に、ハコベ(
STE)、ヤエムグラ(GAL)、スミレ(VIO)、
イヌカミツレ(MAT)、ノスズメノテッポウ(ALO
)、小麦(アバロン品種:TRZ−1、ハンツマン品種
:TRZ−2)及び大麦(HOR)の各種子を播種し、
0.5〜1cmに覆土した。ポットは屋外に静置し、2
ヶ月間育成した。その後、実施例3により調製した水和
剤の所定量をヘクタール当り250リットルの水で希釈
し(展着剤0.1%加用)、茎葉表面に小型噴霧器で均
一に散布した。なお、薬剤処理時の各植物の草丈は、小
麦28〜36cm、大麦20〜32cm、雑草4〜15
cmであった。薬剤処理後40日目に、供試植物の地上
部生体重を測定し、無処理区に対する生育抑制率(%)
を算出した。結果を表2に示した。
Next, the effects of the herbicidal composition of the present invention will be specifically explained with reference to test examples. Test example 1 (field crop foliage treatment) Chickweed (chickweed) was placed in each pot (800 cm2) filled with soil.
STE), Yaemugura (GAL), Sumire (VIO),
Dogtail (MAT), Japanese Sparrow (ALO)
), wheat (Avalon variety: TRZ-1, Huntsman variety: TRZ-2), and barley (HOR) seeds were sown,
It was covered with soil to a thickness of 0.5 to 1 cm. Place the pot outdoors, and
It was cultivated for a month. Thereafter, a predetermined amount of the wettable powder prepared in Example 3 was diluted with 250 liters of water per hectare (0.1% spreading agent was added) and uniformly sprayed onto the foliage surface using a small sprayer. The plant height of each plant upon chemical treatment was 28 to 36 cm for wheat, 20 to 32 cm for barley, and 4 to 15 cm for weeds.
It was cm. On the 40th day after chemical treatment, the weight of the above-ground parts of the test plants was measured, and the growth inhibition rate (%) compared to the untreated area was determined.
was calculated. The results are shown in Table 2.

【0022】[0022]

【表2】[Table 2]

【0023】試験例2 土壌を充填した各ポット(800cm2)に、ハコベ(
STE)、オオイヌノフグリ(VER)、ヤエムグラ(
GAL)、スミレ(VIO)、イヌカミツレ(MAT)
、ノスズメノテッポウ(ALO)、小麦(アバロン品種
:TRZ−1、ハンツマン品種:TRZ−2)及び大麦
(HOR)の各種子を播種し、0.5〜1cmに覆土し
た。ポットは屋外に静置し、2ヶ月間育成した。その後
、実施例4により調製した水和剤の所定量をヘクタール
当り250リットルの水で希釈し(展着剤0.1%加用
)、茎葉表面に小型噴霧器で均一に散布した。なお、薬
剤処理時の各植物の草丈は、小麦25〜30cm、大麦
10〜12cm、雑草2〜6cmであった。薬剤処理後
40日目に供試植物の地上部生体重を測定し、無処理区
に対する生育抑制率(%)を算出した。結果を表3に示
した。
Test Example 2 Each pot (800 cm2) filled with soil was planted with chickweed (
STE), Giant dogfish (VER), Yaemugura (
GAL), violet (VIO), dog violet (MAT)
Seeds of , ALO (ALO), wheat (Avalon variety: TRZ-1, Huntsman variety: TRZ-2), and barley (HOR) were sown and covered with soil to a thickness of 0.5 to 1 cm. The pot was placed outdoors and grown for two months. Thereafter, a predetermined amount of the wettable powder prepared in Example 4 was diluted with 250 liters of water per hectare (0.1% spreading agent was added) and uniformly sprayed onto the foliage surface using a small sprayer. The plant height of each plant at the time of chemical treatment was 25 to 30 cm for wheat, 10 to 12 cm for barley, and 2 to 6 cm for weeds. On the 40th day after the chemical treatment, the weight of above-ground parts of the test plants was measured, and the growth inhibition rate (%) was calculated relative to the untreated plot. The results are shown in Table 3.

【0024】[0024]

【表3】[Table 3]

【0025】[0025]

【発明の効果】以上の通り、発明の除草剤組成物は、一
般式〔I〕にて表されるビスピリミジニルオキシ安息香
酸誘導体から選ばれた1種に2,4−DあるいはMCP
から選ばれた1種を配合することによって、当該ビスピ
リミジニルオキシ安息香酸誘導体の麦類に対する薬害を
回避しがたい条件下で用いても、各々の有効成分の除草
効果を低下させることなく、薬害を選択的にかつ顕著に
軽減させるという選択的薬害軽減効果を有する。
Effects of the Invention As described above, the herbicidal composition of the invention contains 2,4-D or MCP in one selected from the bispyrimidinyloxybenzoic acid derivatives represented by the general formula [I].
By blending one selected from the following, even when the bispyrimidinyloxybenzoic acid derivative is used under conditions where it is difficult to avoid phytotoxicity to wheat, the herbicidal effect of each active ingredient will not be reduced, and the phytotoxicity will be reduced. It has the effect of selectively and significantly reducing drug damage.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】  一般式 【化1】 (式中、Rは水素原子、アルカリ金属原子、アルカリ土
類金属原子、アンモニウムイオン、有機アンモニウムイ
オン、CH2OCOC4H9−t基あるいはCH(CH
3)COOC2H5基を示す。)にて表されるビスピリ
ミジニルオキシ安息香酸誘導体から選ばれる1種と2,
4−ジクロルフェノキシ酢酸もしくはその塩またはその
エステル、あるいは2−メチル−4−クロルフェノキシ
酢酸もしくはその塩またはそのエステルから選ばれる1
種と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。
Claim 1: General formula [Formula 1] (wherein R is a hydrogen atom, an alkali metal atom, an alkaline earth metal atom, an ammonium ion, an organic ammonium ion, a CH2OCOC4H9-t group, or a CH(CH
3) Shows COOC2H5 group. ) and 2 selected from the bispyrimidinyloxybenzoic acid derivatives represented by
1 selected from 4-dichlorophenoxyacetic acid or its salt or its ester, or 2-methyl-4-chlorophenoxyacetic acid or its salt or its ester
A herbicidal composition characterized by containing seeds as an active ingredient.
JP5774091A 1991-03-01 1991-03-01 Herbicide composition Expired - Lifetime JP2974806B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5774091A JP2974806B2 (en) 1991-03-01 1991-03-01 Herbicide composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5774091A JP2974806B2 (en) 1991-03-01 1991-03-01 Herbicide composition

Publications (2)

Publication Number Publication Date
JPH04275201A true JPH04275201A (en) 1992-09-30
JP2974806B2 JP2974806B2 (en) 1999-11-10

Family

ID=13064313

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5774091A Expired - Lifetime JP2974806B2 (en) 1991-03-01 1991-03-01 Herbicide composition

Country Status (1)

Country Link
JP (1) JP2974806B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102461507A (en) * 2010-11-19 2012-05-23 南京华洲药业有限公司 Mixed herbicide composition containing bispyribac-sodium and acetochlor and application thereof
CN102461545A (en) * 2010-11-19 2012-05-23 南京华洲药业有限公司 Mixed weeding composition containing bispyribac-sodium and cyclosulfamuron

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107683858A (en) * 2017-09-19 2018-02-13 浙江天丰生物科学有限公司 A kind of complex herbicidal composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102461507A (en) * 2010-11-19 2012-05-23 南京华洲药业有限公司 Mixed herbicide composition containing bispyribac-sodium and acetochlor and application thereof
CN102461545A (en) * 2010-11-19 2012-05-23 南京华洲药业有限公司 Mixed weeding composition containing bispyribac-sodium and cyclosulfamuron

Also Published As

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JP2974806B2 (en) 1999-11-10

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