JPH08245321A - Herbicide composition for paddy field - Google Patents

Herbicide composition for paddy field

Info

Publication number
JPH08245321A
JPH08245321A JP7038477A JP3847795A JPH08245321A JP H08245321 A JPH08245321 A JP H08245321A JP 7038477 A JP7038477 A JP 7038477A JP 3847795 A JP3847795 A JP 3847795A JP H08245321 A JPH08245321 A JP H08245321A
Authority
JP
Japan
Prior art keywords
weight
compound
composition
active ingredient
weeds
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
JP7038477A
Other languages
Japanese (ja)
Other versions
JP3741457B2 (en
Inventor
Kazuo Naohara
一男 直原
Shinji Kawaguchi
真二 川口
Yukiko Oe
由起子 大江
Masatoshi Yokoyama
雅敏 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.)
Bayer CropScience SA
Original Assignee
Rhone Poulenc Agrochimie SA
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 Rhone Poulenc Agrochimie SA filed Critical Rhone Poulenc Agrochimie SA
Priority to JP03847795A priority Critical patent/JP3741457B2/en
Priority to KR1019960004213A priority patent/KR960030788A/en
Publication of JPH08245321A publication Critical patent/JPH08245321A/en
Application granted granted Critical
Publication of JP3741457B2 publication Critical patent/JP3741457B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/82Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/28Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE: To obtain the subject composition containing a dichloropropinyloxyphenyl dimethylethyloxadiazolone, etc., as an active ingredient, capable of controlling a wide range of weeds at low doses, causing no chemical injuries on paddy rice, and excellent in safety to farmers. CONSTITUTION: This herbicidal composition for paddy field contains, as active ingredients, (A) 3-[2,4-dichloro-5-(2-propinyloxy)phenyl]-5-(1,1-dimethylethyl)-1,3,4- oxadiazol-2(3H)-one of formula I and (B) 1-(α,α-dimethylbenzyl)-3-p-tolylurea of formula II in a weight ratio B/A of pref. 1-500, being applied pref. at 0.02-4 kg/ha based on the total amount of the active ingredients.

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し、さ
らに詳しくは、水稲の移植前後に施用することにより水
稲に安全で水田雑草を効果的に防除する水田用除草剤組
成物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a herbicide composition, and more particularly to a herbicide composition for paddy fields which is safe for paddy rice and effectively controls paddy field weeds by being applied before and after transplanting of the rice.

【0002】[0002]

【従来の技術】これまで、水田用として多くの除草剤が
実用化されており、それらは単剤もしくは2種以上の有
効成分を含む混合剤として広く一般に使用されてきた。
しかしながら、これらの剤は一年生雑草には比較的有効
であるものの多年生雑草に対する効果は不足しており、
そのため近年国内の水田でホタルイ、ウリカワ、ミズガ
ヤツリ等の繁殖力の旺盛な多年生雑草が増加の傾向にあ
るのが現状である。
2. Description of the Related Art Up to now, many herbicides have been put to practical use for paddy fields, and they have been widely and generally used as a single agent or a mixed agent containing two or more kinds of active ingredients.
However, although these agents are relatively effective against annual weeds, their effects on perennial weeds are insufficient,
Therefore, in recent years, the number of perennial weeds, such as firefly, sea urchin, and cypress, which have strong reproductive ability, has been increasing in rice fields in Japan.

【0003】[0003]

【発明が解決しようとする問題点】このことから、雑草
の発生が少なく繁殖力の貧困な、水稲の移植前後に施用
することにより、水稲に安全で幅広い雑草を効果的に防
除する水田用除草剤の開発が望まれている。
[Problems to be Solved by the Invention] Therefore, weeding for paddy field which is safe for rice and effectively controls a wide range of weeds by applying it before and after transplanting paddy rice, which causes few weeds and is poor in fertility. The development of agents is desired.

【0004】[0004]

【課題を解決するための手段】本発明者等は、上記の農
業者の要望を満たした水田用除草剤を開発すべく諸種の
検討を行った。その結果、殺草機構及び殺草スペクトラ
ムの異なる2種の化合物を好ましくは特定の比率で組み
合わせることにより、水田における広範囲の雑草を選択
的に防除でき、しかもその除草効力はそれらを単独で用
いる場合に比較して相乗的に増大し、そのため低薬量で
施用でき、さらに殺草スペクトラムが拡大することを見
出し、本発明の除草剤組成物を完するに至った。
[Means for Solving the Problems] The present inventors have conducted various studies to develop a herbicide for paddy fields that meets the above-mentioned demands of farmers. As a result, it is possible to selectively control a wide range of weeds in paddy fields by combining two compounds having different herbicidal mechanisms and spectrums, preferably in a specific ratio, and the herbicidal effect is obtained when they are used alone. It was found that the herbicidal composition of the present invention was completed, and that the herbicidal composition of the present invention was increased by synergistically increasing the amount of the herbicide.

【0005】本発明は、(A)下記式I:The present invention provides (A) the following formula I:

【0006】[0006]

【化3】 Embedded image

【0007】で表される3−[2、4−ジクロロ−5−
(2−プロピニルオキシ)フェニル]−5−(1、1−
ジメチルエチル)−1、3、4−オキサジアゾ−ル−2
(3H)−オン(化合物A)と、(B)下記式II:
3- [2,4-dichloro-5-] represented by
(2-Propinyloxy) phenyl] -5- (1,1-
Dimethylethyl) -1,3,4-oxadiazol-2
(3H) -one (compound A) and (B) the following formula II:

【0008】[0008]

【化4】 [Chemical 4]

【0009】で表される1−(α、α−ジメチルベンジ
ル)−3−p−トリルウレア(化合物B)とを有効成分
として含有することを特徴とする水田用除草剤組成物を
提供するものである。
A herbicidal composition for paddy fields comprising 1- (α, α-dimethylbenzyl) -3-p-tolylurea (compound B) represented by the formula (1) as an active ingredient. is there.

【0010】[0010]

【具体的説明】本発明組成物の有効成分として用いられ
る化合物Aは特開昭48−08936号公報に出願済み
の極低薬量で除草活性を持つ化合物であり、化合物B
は、特公昭48−35454号公報に開示されている公
知の除草剤である。
DETAILED DESCRIPTION OF THE INVENTION Compound A used as an active ingredient of the composition of the present invention is a compound having an extremely low dose of herbicidal activity, which has been filed in JP-A-48-08936.
Is a known herbicide disclosed in JP-B-48-35454.

【0011】本発明組成物において、A成分とB成分の
配合割合は、厳密に制限されるものでなく、最終の除草
剤組成物の適用場所、適用対象、適用時期等によって、
広範囲にわたって変えることができるが、一般には、化
合物A1重量部当たり化合物B0.01〜1000重量
部、好適には1〜500重量部の割合で配合するのが適
当である。
In the composition of the present invention, the blending ratio of the component A and the component B is not strictly limited, and it depends on the application site, application target, application time, etc. of the final herbicide composition.
Although it can be varied over a wide range, it is generally suitable to add 0.01 to 1000 parts by weight, preferably 1 to 500 parts by weight of compound B per 1 part by weight of compound A.

【0012】本発明の組成物を除草剤として実際に用い
る場合、上記有効成分をそれ自体既知の固体ないし液体
の担体もしくは希釈剤、界面活性剤その他の製剤用補助
剤と、それ自体既知の方法で混合して、通常農薬として
用いられる製剤形態、例えば粒剤、乳剤、水和剤、フロ
アブル剤等に調整することができる。
When the composition of the present invention is actually used as a herbicide, the above-mentioned active ingredient is used as a solid or liquid carrier or diluent known per se, a surfactant or other auxiliaries for formulation, and a method known per se. It is possible to prepare a formulation form which is usually used as an agricultural chemical, for example, granules, emulsions, wettable powders, flowable formulations and the like.

【0013】除草剤の製造に際して用い得る固体担体と
しては、カオリナイト群、モンモリナイト群、イライト
群あるいはポリグロスカイト群などで代表されるクレー
群、詳しくはパイロフィライト、アタパルジャイト、セ
ピオライト、カオリナイト、ベントナイト、サポナイ
ト、バーミキュライト、雲母等やタルク及び石こう、炭
酸カルシウム、ドロマイト、けいそう土、方解石、マグ
ネシウム石灰、りん灰石、ゼオライト、無水ケイ酸、合
成ケイ酸カルシウム等の無機物質;大豆粉、タバコ粉、
クルミ粉、小麦粉、木粉、でんぷん、結晶セルロース等
の植物性有機物質;クマロン樹脂、石油樹脂、アルキッ
ド樹脂、ポリ塩化ビニル、ポリアルキレングリコール、
ケトン樹脂、エステルガム、コーバルガム、ダンマルガ
ム等の合成または天然の高分子化合物;カルナバロウ、
蜜ロウ等のワックス類あるいは尿素などが例示できる。
Solid carriers that can be used in the production of herbicides include kaolinite group, montmorillonite group, clay group represented by illite group and polygloskite group, and more specifically, pyrophyllite, attapulgite, sepiolite, kaolinite, Inorganic substances such as bentonite, saponite, vermiculite, mica, talc and gypsum, calcium carbonate, dolomite, diatomaceous earth, calcite, magnesium lime, apatite, zeolite, anhydrous silicic acid, synthetic calcium silicate; soybean powder, tobacco powder,
Vegetable organic substances such as walnut flour, wheat flour, wood flour, starch, crystalline cellulose; coumarone resin, petroleum resin, alkyd resin, polyvinyl chloride, polyalkylene glycol,
Synthetic or natural polymer compounds such as ketone resins, ester gums, cobal gums, dammal gums; carnauba wax,
Examples thereof include waxes such as beeswax and urea.

【0014】適当な液体担体としては、例えば、ケロシ
ン、鉱油、スピンドル油、ホワイトオイル等のパラフィ
ン系もしくはナフテン系炭化水素;キシレン、エチルベ
ンゼン、クメン、メチルナフタリン等の芳香族炭化水
素;トリクロルエチレン、モノクロルベンゼン、o−ク
ロルトルエン等の塩素化炭化水素;ジオキサン、テトラ
ヒドロフランのようなエ−テル類;メチルエチルケト
ン、ジイソブチルケトン、シクロヘキサノン、アセトフ
ェノン、イソホロン等のケトン類;酢酸エチル、酢酸ア
ミル、エチレングリコールアセテート、ジエチレングリ
コールアセテート、マレイン酸ジブチル、コハク酸ジエ
チル等のエステル類;n−ヘキサノール、エチレングリ
コール、ジエチレングリコール、シクロヘキサノール、
ベンジルアルコール等のアルコール類;エチレングリコ
ールエチルエーテル、エチレングリコールフェニルエー
テル、ジエチレングリコールエチルエーテル、ジエチレ
ングリコールブチルエーテル等のエーテルアルコール
類;ジメチルホルムアミド、ジメチルスルホキシド等の
極性溶媒あるいは水等が挙げられる。
Examples of suitable liquid carriers include paraffinic or naphthenic hydrocarbons such as kerosene, mineral oil, spindle oil and white oil; aromatic hydrocarbons such as xylene, ethylbenzene, cumene and methylnaphthalene; trichloroethylene and monochloro. Chlorinated hydrocarbons such as benzene and o-chlorotoluene; ethers such as dioxane and tetrahydrofuran; ketones such as methyl ethyl ketone, diisobutyl ketone, cyclohexanone, acetophenone and isophorone; ethyl acetate, amyl acetate, ethylene glycol acetate, diethylene glycol Esters such as acetate, dibutyl maleate and diethyl succinate; n-hexanol, ethylene glycol, diethylene glycol, cyclohexanol,
Alcohols such as benzyl alcohol; ether alcohols such as ethylene glycol ethyl ether, ethylene glycol phenyl ether, diethylene glycol ethyl ether, and diethylene glycol butyl ether; polar solvents such as dimethylformamide and dimethyl sulfoxide; and water.

【0015】そのほかに有効成分の乳化、分散、湿潤、
拡展、結合、崩壊性調節、有効成分安定化、流動性改
良、防錆等の目的で界面活性剤その他の補助剤を使用す
ることもできる。使用される界面活性剤の例としては、
非イオン性、陰イオン性、陽イオン性および両性イオン
性のいずれの化合物をも使用しうるが、通常は非イオン
性および(または)陰イオン性の化合物が使用される。
適当な非イオン性界面活性剤としては、例えばラウリル
アルコール、ステアリルアルコール、オレイルアルコー
ル等の高級アルコールにエチレンオキシドを重合付加さ
せた化合物;イソオクチルフェノール、ノニルフェノー
ル等のアルキルフェノールにエチレンオキシドを重合付
加させた化合物;ブチルナフトール、オクチルナフトー
ル等のアルキルナフトールにエチレンオキシドを重合付
加させた化合物;パルミチン酸、ステアリン酸、オレイ
ン酸等の高級脂肪酸にエチレンオキシドを重合付加させ
た化合物;ドデシルアミン、ステアリン酸アミド等のア
ミンにエチレンオキシドを重合付加させた化合物;ソル
ビタン等の多価アルコールの高級脂肪酸エステルおよび
それにエチレンオキシドを重合付加させた化合物;エチ
レンオキシドとプロピレンオキシドをブロック重合付加
させた化合物等があげられる。適当な陰イオン性界面活
性剤としては、例えば、ラウリル硫酸ナトリウム、オレ
インアルコール硫酸エステルアミン塩等のアルキル硫酸
エステル塩;スルホこはく酸ジオクチルエステルナトリ
ウム、2−エチルヘキセンスルホン酸ナトリウム等のア
ルキルスルホン酸塩;イソプロピルナフタレンスルホン
酸ナトリウム、メチレンビスナフタレンスルホン酸ナト
リウム、リグニンスルホン酸ナトリウム、ドデシルベン
ゼンスルホン酸ナトリウム等のアリールスルホン酸塩な
どあげられる。さらに本発明の組成物には製剤の性能を
改善し、除草効果を高める目的で、カゼイン、ゼラチ
ン、アルブミン、ニカワ、リグニンスルホン酸塩、アル
ギン酸塩、アラビアゴム、カルボキシメチルセルロー
ス、メチルセルロース、ヒドロキシエチルセルロース、
ポリビニルアルドール、ポリビニルピロリドン、ポリサ
ッカライド等の高分子化合物や他の補助剤を併用するこ
ともできる。
In addition, emulsification, dispersion, wetting of the active ingredient,
Surfactants and other auxiliary agents can be used for the purposes of spreading, binding, controlling disintegration, stabilizing active ingredients, improving fluidity, and preventing rust. Examples of surfactants used include:
Nonionic, anionic, cationic and zwitterionic compounds can be used, but usually nonionic and / or anionic compounds are used.
Suitable nonionic surfactants include, for example, compounds obtained by polymerizing addition of ethylene oxide to higher alcohols such as lauryl alcohol, stearyl alcohol and oleyl alcohol; compounds obtained by polymerizing addition of ethylene oxide to alkylphenols such as isooctylphenol and nonylphenol; butyl. Compounds obtained by polymerizing addition of ethylene oxide to alkylnaphthols such as naphthol and octylnaphthol; Compounds obtained by polymerizing addition of ethylene oxide to higher fatty acids such as palmitic acid, stearic acid and oleic acid; ethylene oxide added to amines such as dodecylamine and stearic acid amide. Polymerization-added compound; higher fatty acid ester of polyhydric alcohol such as sorbitan and compound obtained by polymerization-adding ethylene oxide thereto; Compound propylene oxide was blocked polymerized addition and the like. Suitable anionic surfactants include, for example, alkyl sulphate salts such as sodium lauryl sulphate and oleic alcohol sulphate amine salts; alkyl sulphonates such as sodium sulfosuccinate dioctyl ester and sodium 2-ethylhexene sulphonate. And aryl sulfonates such as sodium isopropyl naphthalene sulfonate, sodium methylenebisnaphthalene sulfonate, sodium lignin sulfonate, and sodium dodecylbenzene sulfonate. The composition of the present invention further improves the performance of the formulation, for the purpose of enhancing the herbicidal effect, casein, gelatin, albumin, glue, lignin sulfonate, alginate, acacia, carboxymethyl cellulose, methyl cellulose, hydroxyethyl cellulose,
Polymer compounds such as polyvinyl aldol, polyvinyl pyrrolidone, and polysaccharides and other auxiliary agents can be used together.

【0016】上記の担体および種種の補助剤は製剤の剤
型、適用場面等を考慮して、目的に応じてそれぞれ単独
あるいは組合わせて適宜使用できる。
The above carriers and various kinds of auxiliary agents can be appropriately used alone or in combination depending on the purpose in consideration of the dosage form of the preparation, the application scene and the like.

【0017】このようにして得られる各種製剤型におけ
る本発明の組成物中の有効成分含有率は製剤型により種
々変化するものであるが、例えば0.01〜99重量
%、好ましくは0.1〜80重量%であることができ
る。
The content of the active ingredient in the composition of the present invention in the various dosage forms thus obtained varies depending on the dosage form, but is, for example, 0.01 to 99% by weight, preferably 0.1. Can be up to 80% by weight.

【0018】水和剤の場合は、例えば有効成分を通常1
〜90重量%含有し、残部は固体担体、分散湿潤剤であ
って、必要に応じて保護コロイド剤、消泡剤等が加えら
れる。
In the case of a wettable powder, for example, the active ingredient is usually 1
The content is ˜90% by weight, and the balance is a solid carrier and a dispersion wetting agent, and a protective colloid agent, a defoaming agent and the like are added if necessary.

【0019】粒剤の場合は、例えば有効成分を通常0.
01〜35重量%含有し、残部は固体担体及び界面活性
剤等である。有効成分は固体担体と均一に混合されてい
るが、あるいは固体担体の表面に均一に固着もしくは吸
着されており、粒の径は約0.2ないし1.5mm程度で
ある。
In the case of granules, for example, the active ingredient is usually added in an amount of 0.
The content is 01 to 35% by weight, and the rest is a solid carrier and a surfactant. The active ingredient is uniformly mixed with the solid carrier, or is fixed or adsorbed uniformly on the surface of the solid carrier, and the particle diameter is about 0.2 to 1.5 mm.

【0020】フロアブル剤の場合は、例えば有効成分を
通常0.5〜50重量%含有しており、これに3ないし
10重量%の分散湿潤剤が含まれ、残部は水であり、必
要に応じて保護コロイド剤、防腐剤、消泡剤等が加えら
れる。
In the case of a flowable agent, for example, the active ingredient is usually contained in an amount of 0.5 to 50% by weight, the dispersion wetting agent is contained in an amount of 3 to 10% by weight, and the balance is water. A protective colloid agent, an antiseptic agent, an antifoaming agent and the like are added.

【0021】上記の如く調製される本発明の組成物の施
用適量は、気象条件、土壌条件、薬剤の製剤形態、対象
作物、対象雑草、施用時期、施用方法等の違いにより一
概に規定できないが、通常、有効成分の合計量を基準に
して1ヘクタール当り0.01〜10kg、好ましくは
0.02〜4kgの範囲が適当である。さらに、本発明の
組成物には、他の殺虫剤、殺菌剤、植物生長調節剤など
を適宜配合することにより、省力防除剤とすることがで
きる。
The appropriate application amount of the composition of the present invention prepared as described above cannot be unconditionally specified due to differences in meteorological conditions, soil conditions, drug formulation, target crops, target weeds, application time, application method and the like. Usually, 0.01 to 10 kg per hectare, based on the total amount of active ingredients, preferably
A range of 0.02-4 kg is suitable. Furthermore, the composition of the present invention can be used as a labor-saving control agent by appropriately adding other insecticides, fungicides, plant growth regulators and the like.

【0022】また必要に応じて散布時に他の各種殺虫
剤、殺菌剤、植物生長調節剤、除草剤及び肥料などの薬
剤と混合使用も可能である。
Further, if necessary, it can be mixed and used with other various insecticides, fungicides, plant growth regulators, herbicides, fertilizers and the like during spraying.

【0023】以下に、本発明を実施例により具体的に説
明する。
The present invention will be specifically described below with reference to examples.

【0024】[0024]

【実施例】【Example】

実施例1 (フロアブル剤) 化合物A 1.2重量% 化合物B 40重量% ポリオキシエチレンノニルフェニルエーテル 2重量% ジオクチルスルホこはく酸ナトリウム 2重量% ザンサンガム 0.2重量% 水 54.6重量% 以上を湿式ボールミルにて湿式粉砕してフロアブル剤を
得た。
Example 1 (flowable agent) Compound A 1.2% by weight Compound B 40% by weight Polyoxyethylene nonylphenyl ether 2% by weight Sodium dioctylsulfosuccinate 2% by weight Zansan gum 0.2% by weight Water 54.6% by weight or more A flowable agent was obtained by wet grinding with a wet ball mill.

【0025】実施例2 (乳剤) 化合物A 1.2重量% 化合物B 40重量% ポリオキシエチレンスチリルフェニルエーテル 3重量% ドデシルベンゼンスルホン酸カルシウム 3重量% キシレン 52.8重量% 以上を均一溶解し乳剤を得た。Example 2 (Emulsion) 1.2% by weight of compound A 40% by weight of compound B 3% by weight of polyoxyethylene styrylphenyl ether 3% by weight of calcium dodecylbenzenesulfonate 3% by weight of xylene Got

【0026】実施例3 (水和剤) 化合物A 1.2重量% 化合物B 40重量% リグニンスルホン酸ナトリウム 3重量% ジアルキルナフタレンスルホン酸ナトリウム 3重量% カオリン 52.8重量% 以上を混合粉砕して水和剤を得た。Example 3 (Wettable powder) Compound A 1.2% by weight Compound B 40% by weight Sodium ligninsulfonate 3% by weight Sodium dialkylnaphthalenesulfonate 3% by weight Kaolin 52.8% by weight The above components were mixed and pulverized. A wettable powder was obtained.

【0027】実施例4 (粒剤) 化合物A 0.6重量% 化合物B 20重量% リグニンスルホン酸ナトリウム 3重量% アルキルナフタレンスルホン酸ナトリウム 1重量% ベントナイト 30重量% タルク 45.4重量% 以上を混合粉砕後、造粒機にて通常の方法によって造粒
し、乾燥して粒剤を得た。
Example 4 (Granule) Compound A 0.6% by weight Compound B 20% by weight Sodium ligninsulfonate 3% by weight Sodium alkylnaphthalenesulfonate 1% by weight Bentonite 30% by weight Talc 45.4% by weight or more After pulverization, the granules were granulated by a usual method with a granulator and dried to obtain granules.

【0028】次に、本発明組成物の効果を試験例をあげ
て具体的に示す。
Next, the effects of the composition of the present invention will be concretely shown with reference to test examples.

【0029】試験例1 (混合による土壌混和処理の薬量低減効果)面積0.2
5m2 のコンクリ−トポットに水田土壌及び化成肥料を
入れ、適量の水を加えて充分にかき混ぜて水田の状態に
した。これに予め温室内で生育させた2葉期の水稲苗を
2本1株としてポット当たり3株移植して、ノビエ、コ
ナギ、アゼナ、ホタルイの種子を一定量づつ播種し、ミ
ズガヤツリの塊茎を一定量づつ植え付けた。
Test Example 1 (Effect of soil mixing treatment to reduce the amount of drug) Area 0.2
The paddy soil and the chemical fertilizer were put in a 5 m 2 concrete pot, an appropriate amount of water was added, and the mixture was thoroughly stirred to make a paddy field. Two 2-leaf stage paddy rice seedlings, which had been grown in the greenhouse in advance, were transplanted to each of these 3 plants per pot, and seeds of Novier, Konagi, Azena, and Firefly were sown in fixed amounts, and the tubers of Cyperus japonicus were fixed. Planted in quantities.

【0030】移植4日前に、供試化合物の所定量をフロ
アブル剤(実施例1に準拠して製剤した)を用いて処理
した。
Four days before transplantation, a predetermined amount of the test compound was treated with a flowable agent (prepared according to Example 1).

【0031】薬剤処理30日後に殺草効果及び水稲薬害
程度を調査した結果を表1に示す。
Table 1 shows the results of an investigation of the herbicidal effect and the degree of damage to paddy rice after 30 days from the chemical treatment.

【0032】[0032]

【表1】 [Table 1]

【0033】なお、表中各草種に対する殺草効果及び水
稲薬害程度は、下記の殺草効果及び水稲薬害程度の表2
の通り、それぞれ「0」から「5」までの6段階の評
点、及び「−」から「×」までの6段階の符号で表し
た。
In the table, the herbicidal effect and the degree of phytotoxicity against paddy rice are shown in Table 2 below.
As shown in the table, each grade is represented by 6 grades from "0" to "5" and 6 grades from "-" to "x".

【0034】[0034]

【表2】 [Table 2]

【0035】試験例2 (混合による茎葉兼土壌処理の薬量低減効果)試験例1
と同様の方法にて試験ポットを用意し、移植3日後に供
試化合物の所定量を粒剤(実施例4に準拠して製剤し
た)を用いて処理した。
Test Example 2 (Effect of reducing the dose of foliage / soil treatment by mixing) Test Example 1
A test pot was prepared by the same method as described in (3) above, and 3 days after transplantation, a predetermined amount of the test compound was treated with granules (prepared according to Example 4).

【0036】薬剤処理30日後に殺草効果及び水稲薬害
程度を調査した結果を表3に示す。
Table 3 shows the results of an investigation of the herbicidal effect and the degree of damage to paddy rice after 30 days from the chemical treatment.

【0037】[0037]

【表3】 [Table 3]

【0038】なお、表中各草種に対する殺草効果及び水
稲薬害程度は、上記の殺草効果及び水稲薬害程度の表2
の通り、それぞれ「0」から「5」までの6段階の評
点、及び「−」から「×」までの6段階の符号で表し
た。
In the table, the herbicidal effect and the degree of phytotoxicity to paddy rice are shown in Table 2 of the above herbicidal effect and the degree of phytotoxicity to paddy rice.
As shown in the table, each grade is represented by 6 grades from "0" to "5" and 6 grades from "-" to "x".

【0039】これらの結果から本発明組成物はそれぞれ
の有効成分をそれぞれ単独で用いた場合に比べて、極め
て低い薬量で各種雑草を防除できることがわかった。
From these results, it was found that the composition of the present invention can control various weeds with an extremely low dose as compared with the case where each active ingredient is used alone.

【0040】以上の試験例1及び2の結果が示すよう
に、本発明組成物は、これまでの除草剤には例をみない
低薬量で諸雑草を有効に防除することができ、農業用資
材として極めて有望である。
As shown by the results of Test Examples 1 and 2 above, the composition of the present invention can effectively control various weeds with a low dose which is unprecedented in herbicides. It is extremely promising as a material for use.

【0041】[0041]

【発明の効果】本発明組成物は、上記の試験例から明ら
かなように、各化合物単独では到底できないような低薬
量でノビエ、アゼナ、コナギ、ホタルイ、ミズガヤツリ
等の広汎な雑草に高い除草効果を示し、かつ水稲に対し
て全く薬害を与えない。
As is apparent from the above test examples, the composition of the present invention has high herbicidal activity against a wide range of weeds such as Nobie, Azena, Kokonagi, Firefly, Mizugaya, etc. in such a low dose that each compound alone cannot achieve it. It is effective and has no phytotoxicity to paddy rice.

【0042】また、使用時期は、水稲移植前から雑草生
育初期(移植後約20日)までの広い範囲から任意に選
定できるが、その中でも雑草の発生前から発生始期(移
植前7日から移植後10日ごろまで)に処理すると最も
高い除草効果を得ることができる。
The time of use can be arbitrarily selected from a wide range from before transplantation of rice to early growth of weeds (about 20 days after transplantation). The highest herbicidal effect can be obtained when the treatment is performed about 10 days later.

【0043】これらの優れた効果は明らかに本発明組成
物に含有されるそれぞれの有効成分の間に強力な相乗効
果が存在することを示すものであり、それぞれ単独の除
草特性からは全く予想されない効果を示すものである。
These excellent effects clearly indicate that there is a strong synergistic effect between the respective active ingredients contained in the composition of the present invention, which is completely unexpected from the herbicidal properties of each of them. It shows the effect.

【0044】また、本発明組成物は、各有効成分単独の
殺草力が高く、さらに強力な相乗効果が存在することに
より、これまでの除草剤に比べて有効成分投下量が極め
て少なくてすむ。それゆえ環境や農業者に対する安全性
も高く、時代の要望に合致した除草剤であるといえる。
In addition, the composition of the present invention has a high herbicidal activity of each active ingredient alone and has a strong synergistic effect, so that the amount of the active ingredient applied can be extremely small as compared with conventional herbicides. . Therefore, it is safe to the environment and farmers, and can be said to be a herbicide that meets the needs of the times.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 大江 由起子 茨城県稲敷郡阿見町中央8−3−1 ロー ヌ・プーラン油化アグロ株式会社 阿見研 究所内 (72)発明者 横山 雅敏 茨城県稲敷郡阿見町中央8−3−1 ロー ヌ・プーラン油化アグロ株式会社 阿見研 究所内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Yukiko Oe Inventor Yukiko Oe 8-3-1 Chuo, Ami-machi, Inashiki-gun, Ibaraki Rhone Poulin Petrochemical Agro Co., Ltd. Ami Research Laboratory (72) Inventor Masatoshi Yokoyama Inashiki-gun, Ibaraki Prefecture 8-3-1 Chuo, Ami Town Rhone Poulin Petrochemical Agro Co., Ltd. Ami Research Laboratory

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 (A)下記式(I) 【化1】 で表される3−[2、4−ジクロロ−5−(2−プロピ
ニルオキシ)フェニル]−5−(1、1−ジメチルエチ
ル)−1、3、4−オキサジアゾ−ル−2(3H)−オ
ンと、(B)下記式II 【化2】 で表される1−(α、α−ジメチルベンジル)−3−p
−トリルウレアとを有効成分として含有することを特徴
とする水田用除草剤組成物。
1. (A) The following formula (I): 3- [2,4-dichloro-5- (2-propynyloxy) phenyl] -5- (1,1-dimethylethyl) -1,3,4-oxadiazol-2 (3H)-represented by When turned on, (B) the following formula II: 1- (α, α-dimethylbenzyl) -3-p represented by
-A herbicide composition for paddy fields containing tolylurea as an active ingredient.
JP03847795A 1995-02-27 1995-02-27 Herbicide composition for paddy field Expired - Lifetime JP3741457B2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP03847795A JP3741457B2 (en) 1995-02-27 1995-02-27 Herbicide composition for paddy field
KR1019960004213A KR960030788A (en) 1995-02-27 1996-02-22 Herbicidal herbicide composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP03847795A JP3741457B2 (en) 1995-02-27 1995-02-27 Herbicide composition for paddy field

Publications (2)

Publication Number Publication Date
JPH08245321A true JPH08245321A (en) 1996-09-24
JP3741457B2 JP3741457B2 (en) 2006-02-01

Family

ID=12526345

Family Applications (1)

Application Number Title Priority Date Filing Date
JP03847795A Expired - Lifetime JP3741457B2 (en) 1995-02-27 1995-02-27 Herbicide composition for paddy field

Country Status (2)

Country Link
JP (1) JP3741457B2 (en)
KR (1) KR960030788A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998054967A1 (en) * 1997-06-05 1998-12-10 Isagro Ricerca S.R.L. Herbicidal compositions

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56166104A (en) * 1980-05-23 1981-12-21 Nissan Chem Ind Ltd Herbicidal composition for paddy field
JPS5892602A (en) * 1981-11-27 1983-06-02 Mitsubishi Chem Ind Ltd Herbicide composition
JPH0655650B2 (en) * 1984-11-06 1994-07-27 三共株式会社 Herbicide composition
JPS6245505A (en) * 1985-08-26 1987-02-27 Japan Carlit Co Ltd:The Herbicide for paddy field
JPH0617287B2 (en) * 1986-05-09 1994-03-09 三共株式会社 Herbicide
JPH0597614A (en) * 1991-10-01 1993-04-20 Nissan Chem Ind Ltd Herbicide composition
JP3545037B2 (en) * 1994-04-11 2004-07-21 三共アグロ株式会社 Herbicidal composition for paddy fields

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998054967A1 (en) * 1997-06-05 1998-12-10 Isagro Ricerca S.R.L. Herbicidal compositions

Also Published As

Publication number Publication date
JP3741457B2 (en) 2006-02-01
KR960030788A (en) 1996-09-17

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