JPS6116244B2 - - Google Patents

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Publication number
JPS6116244B2
JPS6116244B2 JP11230980A JP11230980A JPS6116244B2 JP S6116244 B2 JPS6116244 B2 JP S6116244B2 JP 11230980 A JP11230980 A JP 11230980A JP 11230980 A JP11230980 A JP 11230980A JP S6116244 B2 JPS6116244 B2 JP S6116244B2
Authority
JP
Japan
Prior art keywords
compound
parts
weeds
test
herbicidal
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.)
Expired
Application number
JP11230980A
Other languages
Japanese (ja)
Other versions
JPS5636403A (en
Inventor
Jiutaro Tamura
Toshimitsu Kurihara
Takuo Ooi
Hiroshi Ooyama
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.)
Hokko Chemical Industry Co Ltd
Original Assignee
Hokko 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 Hokko Chemical Industry Co Ltd filed Critical Hokko Chemical Industry Co Ltd
Priority to JP11230980A priority Critical patent/JPS5636403A/en
Publication of JPS5636403A publication Critical patent/JPS5636403A/en
Publication of JPS6116244B2 publication Critical patent/JPS6116244B2/ja
Granted legal-status Critical Current

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  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

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

本発明は2,4−ジクロル−3′−カーボメトキ
シ−4′−ニトロフエニルエーテル(以下「化合物
(1)」という)または2,4,6−トリクロルフエ
ニル−3′−カーボメトキシ−4′−ニトロフエニル
エーテルと2−メチル−4−クロルフエニル−
3′−カーボメトキシ−4′−ニトロフエニルエーテ
ル(以下「化合物(2)」という)と2−メチル−4
−クロルフエノキシ酢酸(以下化合物A」とい
う)とを含有することを特徴とする除草剤組成物
に関する。 本発明に係る除草剤の特徴は、異つた殺草活性
を有する除草剤を混合することにより、近時爆発
的に蔓延繁茂を極め殺滅困難であつて各地で防除
対策が重大な課題となつている多年生雑草のウリ
カワに対して、極めて高い相乗的殺草効果を示す
ことにある。 従来、2,4−ジクロルフエノキシ酢酸、ペン
タクロルフエノール、2,6−ジクロルベンゾニ
トリル、2,4−ピス(イソプロピルアミノ)−
6−メチルチオ−1,3,5,−トリアジン、
2,4−ジクロフエニル−4′−ニトロフエニルエ
ーテル、2,4,6−トリクロルフエニル、−
4′−ニトロフエニルエーテル、パラクロルベンジ
ルN,N−ジエチルチオールカーバメートなどの
多くの水田用除草剤が開発され広く使用されてき
た。 今日では人蓄毒性、魚毒および薬害の強い除草
剤は著しく使用を制限され、これに代つて安全で
かつヒエ、マツバイなどの雑草に対して極めて除
草効果の高い薬剤が次々と開発されており、農業
労働力の不足の折から除草剤の使用は実に大きく
貢献している。 しかしながら、最近除草対策が各地で問題とな
つている多年生雑草のウリカワには既存の除草剤
はほとんど除草活性を示さず、また他の雑草が除
草されると相互の競合作用が除去されるためにウ
リカワは爆発的に蔓延繁茂する。 ウリカワは早春塊茎から発芽し、地下茎を出し
増殖し、その年の越冬塊茎は春の1個が秋末には
約750個になり、翌年の塊茎は55万個にもなる。
塊茎は春期水田に水を入れ耕転すると浮き易く、
春先もしも1個の塊茎の侵入があれば生育条件が
よければ3年後には4億個以上の塊茎となる。数
年前瀬戸内でウリカワに対する関心がもたれて以
来、今日では日本全国のほとんどの県に侵入し、
稲作に対し甚大な被害を与え、益々急速に繁茂し
つつあるので、ヒエ、マツバイなどの雑草の防除
は勿論のこと、ウリカワに対しても極めて効果的
に防除できる薬剤の開発が急務とされ強く要望さ
れている。 本発明者等は駆除困難なウリカワに対して適確
な除草作用を有し、しかも人蓄および魚貝類に対
して無毒で、作物に対しても薬害がなく安全に防
除できる薬剤を開発する目的で多くの化合物を供
試した。その結果、化合物(1)または化合物(2)と化
合物Aとを有効成分として含有する除草剤組成物
が水田のウリカワに対して極めて除草活性が高
く、2薬剤が互いに除草効力を増加させあつて相
乗的に除草効力を発揮しうることを見い出した。 化合物(1)または化合物(2)は発生前後のイネ科雑
草であるタイヌビエおよび大部分の一年生広葉雑
草に対して極めて防除効果が高く、移植水稲に対
して薬害の少ない優れた水稲田除草剤である。ま
た多年生雑草のウリカワの発生前に薬剤を施用し
た場合に高い殺草性が認められている。しかしな
がら、実用的にはウリカワを完全に防除し得る薬
量を投入した場合には水稲に対する薬害が発生す
るなどの問題があつた。また化合物Aは水稲の一
年生雑草、例えばコナギ、キカシグサには極めて
高い防除効力を有することが知られている。ま
た、化合物Aは多年生雑草のウリカワにも若干の
殺草作用が認められるが、実用的には単剤で防除
することは極めて困難であり、また他の多年生雑
草であるマツバイ、ヒルムシロ、ミズガヤツリな
どに対しても常用量では完全に枯殺しえない薬剤
である。 本発明は有効成分として、化合物(1)または化合
物(2)と化合物Aとを施用することによつてコナ
ギ、アゼナ、タイヌビエ、キカシグサなどに対し
て高い除草効果を有することは勿論、従来防除困
難であつたウリカワに対して従来の薬剤では予想
もできなかつた程顕著な相乗的除草効果を有して
いる。本発明におけるこのような事実は全く新し
い知見である。 本発明に使用される有効成分の配合割合は、重
量部(以下部という)で化合物(1)または化合物(2)
1部に対して化合物Aを30分の1部乃至3分の1
部配合するのが適当であるが、必要に応じてさら
に適当な配合とすることができる。さらに他の除
草剤と混合施用できることは勿論、殺菌剤や殺虫
剤、植物調節剤、肥料などと混合して使用すれば
省力防除剤として使用できる。 前記のように配合したものは各種の担体と混合
して通常の農薬に使用される形態、例えば乳剤、
粒剤、水和剤などの形態に製剤化できる。これに
使用される担体としては、タルク、クレー、ベン
トナイトなどの固体担体、アルコール類、ベンゼ
ン、キシレン、アセトン、ソルベントナフサなど
の液体担体など一般に広く使用されているものが
使用される。また展着剤、乳化剤、湿展剤、固着
剤などの各種の補助剤を必要に応じて加えること
ができる。 次に本発明の除草剤組成物の実施例を若干示す
が、本発明は以下の実施例のみに限定されるもの
ではない。 実施例1 粒剤 化合物(2)7部、化合物A0.7部、ベントナイト
10部、ドデシルベンゼンスルホン酸ソーダ2部お
よびクレー80.3部を混合し、造粒機を用いて粒剤
とした。 実施例2 乳剤 化合物(2)18部、化合物A1.5部、キシレン31
部、アセトン42.5部およびポリオキシエチレン)
ニルフエニルエーテル7部を均一に混合して乳剤
とした。 実施例3 粒剤 化合物(1)9部、化合物A1.4部、2,4−ビス
(エチルアミノ)−6−メチルチオ−1,3,5−
トリアジン2部、ベントナイト8部、ドデシルベ
ンゼンスルホン酸ソーダ2部およびクレー77.6部
を混合し、造粒機を用いて粒剤とした。 次に本発明に係る除草剤組成物につき試験例を
示す。 試験例1 ウリカワに対する防除効力試験 試験方法として5000分の1アールの大きさワグ
ネルポツトに沖積粘質の水田土壌をつめ、その発
層部にウリカワ塊茎をポツト当り10粒ずつ移植
し、そして湛水深3cmに保つた。その後ウリカワ
の発生直前に供試薬剤の所定量を滴下処理した。
本試験は1濃度3ポツト制に行つた。調査は薬剤
を処理した後30日目に生き残り残草を抜き取り乾
燥重量を測定し、その平均重量から下式により除
草率(%)を算出した。 除草率=(1−処理区平均乾重量/無処理平均乾重量
)×100 その結果は第1表のとおりである。
The present invention relates to 2,4-dichloro-3'-carbomethoxy-4'-nitrophenyl ether (hereinafter referred to as "compound").
(1)) or 2,4,6-trichlorophenyl-3'-carbomethoxy-4'-nitrophenyl ether and 2-methyl-4-chlorophenyl-
3'-carbomethoxy-4'-nitrophenyl ether (hereinafter referred to as "compound (2)") and 2-methyl-4
- Chlorphenoxyacetic acid (hereinafter referred to as "Compound A"). A feature of the herbicide according to the present invention is that, by mixing herbicides with different herbicidal activities, the herbicide has recently spread explosively and become extremely difficult to kill, making control measures a serious issue in various places. It exhibits an extremely high synergistic herbicidal effect against the perennial weed Prunus elegans. Conventionally, 2,4-dichlorophenoxyacetic acid, pentachlorophenol, 2,6-dichlorobenzonitrile, 2,4-pis(isopropylamino)-
6-methylthio-1,3,5-triazine,
2,4-Dichlorophenyl-4'-nitrophenyl ether, 2,4,6-trichlorophenyl, -
Many herbicides for rice fields, such as 4'-nitrophenyl ether and parachlorobenzyl N,N-diethylthiol carbamate, have been developed and widely used. Nowadays, the use of herbicides that are toxic to humans, toxic to fish, and highly phytotoxic has been severely restricted, and in their place, safe and extremely effective herbicides against weeds such as barnyard grass and grasshopper are being developed one after another. , the use of herbicides has made a significant contribution to the agricultural labor shortage. However, existing herbicides have almost no herbicidal activity against the perennial weed, which has recently become a problem in many areas, and when other weeds are removed, mutual competitive effects are eliminated. Urikawa spreads and flourishes explosively. Urikawa sprouts from tubers in early spring, sends out underground stems, and proliferates, and the number of overwintering tubers that year grows from one in spring to about 750 by the end of autumn, and as many as 550,000 the following year.
Tubers tend to float when paddy fields are filled with water in spring and tilled.
If one tuber invades in early spring, if growing conditions are good, three years later there will be more than 400 million tubers. Since interest in Urikawa arose in Setouchi a few years ago, it has now invaded most prefectures across Japan.
As it causes tremendous damage to rice crops and is rapidly growing, there is an urgent need to develop a chemical that can not only control weeds such as barnyard grass and Japanese grasshopper, but also highly effective control of weeds. It is requested. The purpose of the present inventors is to develop a drug that has an appropriate herbicidal effect on the hard-to-get rid of Prunus elegans, is non-toxic to humans and fish and shellfish, and is safe and harmless to crops. Many compounds were tested. As a result, it was found that a herbicidal composition containing compound (1) or compound (2) and compound A as active ingredients had extremely high herbicidal activity against paddy field grass, and that the two drugs mutually increased the herbicidal efficacy. It has been found that these compounds can exhibit synergistic herbicidal effects. Compound (1) or compound (2) has an extremely high control effect on the grass weed grass grass weed before and after emergence, as well as most annual broad-leaved weeds, and is an excellent rice field herbicide with little chemical damage to transplanted rice. be. In addition, high herbicidal properties have been observed when the chemical is applied before the emergence of the perennial weed lily. However, in practice, there were problems such as phytotoxicity to paddy rice when a dosage sufficient to completely control Paddy was used. Compound A is also known to have an extremely high control effect on annual weeds of paddy rice, such as Prunus japonicus and Kikashigusa. In addition, although Compound A has a slight herbicidal effect on the perennial weed Cucumber, it is extremely difficult to control it with a single agent in practical terms. However, it is a drug that cannot be completely killed at regular doses. By applying Compound (1) or Compound (2) and Compound A as active ingredients, the present invention not only has a high herbicidal effect on grasshopper, Japanese azalea, Japanese millet, and Kikashigusa, but also controls conventionally difficult to control herbivores. It has a synergistic herbicidal effect that was unimaginable with conventional agents against the common weed. This fact in the present invention is a completely new finding. The blending ratio of the active ingredients used in the present invention is compound (1) or compound (2) in parts by weight (hereinafter referred to as parts).
1 part to 1/30th part of compound A
Although it is appropriate to mix 1 part, it is possible to make a more suitable mix if necessary. Furthermore, it can of course be used in combination with other herbicides, and can also be used as a labor-saving pest control agent if used in combination with fungicides, insecticides, plant regulators, fertilizers, etc. The above-mentioned compound is mixed with various carriers to form a form commonly used in agricultural chemicals, such as emulsions,
It can be formulated into granules, wettable powders, etc. As carriers used for this purpose, commonly used carriers include solid carriers such as talc, clay, and bentonite, and liquid carriers such as alcohols, benzene, xylene, acetone, and solvent naphtha. Furthermore, various auxiliary agents such as a spreading agent, an emulsifier, a wetting agent, and a fixing agent can be added as necessary. Next, some examples of the herbicide composition of the present invention will be shown, but the present invention is not limited to the following examples. Example 1 Granules 7 parts of compound (2), 0.7 parts of compound A, bentonite
10 parts of sodium dodecylbenzenesulfonate, 2 parts of sodium dodecylbenzenesulfonate, and 80.3 parts of clay were mixed to form granules using a granulator. Example 2 Emulsion 18 parts of compound (2), 1.5 parts of compound A, 31 parts of xylene
parts, 42.5 parts of acetone and polyoxyethylene)
Seven parts of nil phenyl ether were uniformly mixed to form an emulsion. Example 3 Granules 9 parts of compound (1), 1.4 parts of compound A, 2,4-bis(ethylamino)-6-methylthio-1,3,5-
2 parts of triazine, 8 parts of bentonite, 2 parts of sodium dodecylbenzenesulfonate, and 77.6 parts of clay were mixed and made into granules using a granulator. Next, test examples will be shown regarding the herbicide composition according to the present invention. Test Example 1 Test for control efficacy against Urikawa As a test method, a 1/5000 are size Wagner pot was filled with alluvial clay paddy soil, and 10 Urikawa tubers per pot were transplanted to the emerging layer, and the water depth was 3 cm. I kept it. Thereafter, a predetermined amount of the test chemical was added dropwise immediately before the appearance of swelling.
This test was conducted using a three-pot system at one concentration. In the investigation, on the 30th day after treatment with the chemical, the remaining weeds were extracted and their dry weight was measured, and the weeding rate (%) was calculated from the average weight using the formula below. Weeding rate = (1 - average dry weight of treated area/average dry weight of untreated area) x 100 The results are shown in Table 1.

【表】【table】

【表】 試験例 2 試験方法として水田に1区が10m2の大きさの試
験区をつくり、各区に一定粒数(100粒)のウリ
カワ塊茎および一定量のコナギ、タイヌビエ、キ
カシグサ、マツバイ種子を代掻時に土壌表層に混
和した。そして湛水深を3cmに保ち田植した。そ
してその7日目に供試薬剤の粒剤を実施例に準じ
て調製して散布処理した。調査は薬剤処理30日目
に生き残り雑草を抜きとりその乾燥重量を測定し
た。その結果は第2表のとおりである。
[Table] Test Example 2 As a test method, test plots were created in a rice field with each plot having a size of 10 m 2 , and each plot was seeded with a certain number of tubers (100) and a certain amount of Konagi, Japanese millet, Kikashigusa, and Matsubai seeds. It was mixed into the soil surface layer during puddling. Rice was then planted while keeping the water depth at 3 cm. On the seventh day, granules of the test drug were prepared according to the example and sprayed. In the investigation, surviving weeds were pulled out on the 30th day of chemical treatment and their dry weight was measured. The results are shown in Table 2.

【表】【table】

Claims (1)

【特許請求の範囲】[Claims] 1 2,4−ジクロルフエニル−3′−カーボメト
キシ−4′−ニトロフエニルエーテルまたは2,
4,6−トリクロルフエニル−3′−カーボメトキ
シ−4′−ニトロフエニルエーテルと2−メチル−
4−クロルフエノキシ酢酸エチルとを含有するこ
とを特徴とする除草剤組成物。
1 2,4-dichlorophenyl-3'-carbomethoxy-4'-nitrophenyl ether or 2,
4,6-Trichlorophenyl-3'-carbomethoxy-4'-nitrophenyl ether and 2-methyl-
4-Chlorphenoxyethyl acetate.
JP11230980A 1980-08-16 1980-08-16 Herbicidal composition Granted JPS5636403A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11230980A JPS5636403A (en) 1980-08-16 1980-08-16 Herbicidal composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11230980A JPS5636403A (en) 1980-08-16 1980-08-16 Herbicidal composition

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP48092401A Division JPS5924122B2 (en) 1973-08-20 1973-08-20 herbicide composition

Publications (2)

Publication Number Publication Date
JPS5636403A JPS5636403A (en) 1981-04-09
JPS6116244B2 true JPS6116244B2 (en) 1986-04-28

Family

ID=14583442

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11230980A Granted JPS5636403A (en) 1980-08-16 1980-08-16 Herbicidal composition

Country Status (1)

Country Link
JP (1) JPS5636403A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6064621U (en) * 1983-10-07 1985-05-08 パイオニア株式会社 Electronic NFB type tone control circuit

Also Published As

Publication number Publication date
JPS5636403A (en) 1981-04-09

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