JPS6045505A - Herbicidal composition - Google Patents

Herbicidal composition

Info

Publication number
JPS6045505A
JPS6045505A JP15394983A JP15394983A JPS6045505A JP S6045505 A JPS6045505 A JP S6045505A JP 15394983 A JP15394983 A JP 15394983A JP 15394983 A JP15394983 A JP 15394983A JP S6045505 A JPS6045505 A JP S6045505A
Authority
JP
Japan
Prior art keywords
lower alkyl
weeds
parts
herbicidal composition
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.)
Pending
Application number
JP15394983A
Other languages
Japanese (ja)
Inventor
Takashi Igai
猪飼 隆
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.)
Nissan Chemical Corp
Original Assignee
Nissan Chemical Corp
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 Nissan Chemical Corp filed Critical Nissan Chemical Corp
Priority to JP15394983A priority Critical patent/JPS6045505A/en
Publication of JPS6045505A publication Critical patent/JPS6045505A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:A herbicidal composition obtained by blending a specific pyrazolesulfonylurea derivative and S-(1-methyl-phenetyl)-piperidine-1-carbothioate, showing synergistic effects, effective with a small amount of it used. CONSTITUTION:A herbicidal composition obtained by combining a pyrazolesulfonylurea derivative shown by the formula (A is lower alkyl; B is H, or lower alkyl; R is lower alkyl; X and Y are lower alkyl, or lower alkoxy) (e.g., a compound wherein A, B, R, and X are all Me, and Y is OMe, etc.) with S-(1-methyl- 1-phenetyl)-piperidine-1-carbothioate in a weight ratio of (0.001-10):1. The composition has no phytotoxicity to paddy rice plants, and can control completely Echinochloa crus-galli Beauv. var. praticola Ohwi., weeds from annual to perennial weeds with a small amount of it used.

Description

【発明の詳細な説明】 本発明は一般式(I): 〔式中Aは低級アルキル基を示す。Bは水素原子または
低級アルキル基を示す。Rは低級アルキル基を示す。X
およびYはそれぞれ独立して、低級アルキル基または低
級アルコキシ基を示す。〕 で表されるピラゾールスルボニルウレア誘導体と5−(
1−メチル−1−フェネチル)−ピペリジン−1−カル
ボチオエート(以下MY−93と称する。)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に関する
DETAILED DESCRIPTION OF THE INVENTION The present invention is based on the general formula (I): [In the formula, A represents a lower alkyl group. B represents a hydrogen atom or a lower alkyl group. R represents a lower alkyl group. X
and Y each independently represent a lower alkyl group or a lower alkoxy group. ] Pyrazole sulfonylurea derivative represented by and 5-(
The present invention relates to a herbicidal composition containing 1-methyl-1-phenethyl)-piperidine-1-carbothioate (hereinafter referred to as MY-93) as an active ingredient.

長年にわたる除草剤の研究開発のなかから多種多様な薬
剤が実用化され、これら除草剤は雑草防除作業の省力化
や農園芸作物の生産性向上に寄与してきた。今日におい
ても、より優れた除草特性を有する新規薬剤の開発が要
望され、特に農園芸用除草剤としては、栽培作物に薬害
を及ぼすことなく、対象雑草のみを選択的にかつ低薬量
で防除しうろことが望ましいが、既存の薬剤は必ずしも
この要求を満たすものではなかった。
As a result of many years of research and development into herbicides, a wide variety of herbicides have been put into practical use, and these herbicides have contributed to labor-saving weed control operations and improved productivity of agricultural and horticultural crops. Even today, there is a demand for the development of new chemicals with better herbicidal properties, and in particular, as herbicides for agriculture and horticulture, they are used to selectively control only target weeds at low doses without causing harm to cultivated crops. However, existing drugs do not necessarily meet this requirement.

一般式(1)で表される化合物は従来の除草剤に比して
低薬量で優れた除草効果をあげ、なおかつイネに対して
高い安全性を有する。また、−平生イネ科雑草、−作土
広葉雑草に卓効を示すのみならず、多年生雑草にも強い
効力を示し、その有用性は大きい。
The compound represented by the general formula (1) exhibits excellent herbicidal effects at lower dosages than conventional herbicides, and has high safety against rice. In addition, it is highly effective not only against grassy grass weeds and broad-leaved weeds, but also against perennial weeds, making it highly useful.

また従来より知られている、MY−9,3はノビエ、−
年生雑草に対し、一般式(1)で表される化合物に比し
て高薬量で使用されてきたが、その結果これら−の薬剤
で防除困難な多年生雑草の増加をもたらし、その改善が
望まれている。
In addition, MY-9, 3, which is known from the past, is Nobie, -
Compounds represented by formula (1) have been used against annual weeds in higher doses than the compounds represented by general formula (1), but as a result, there has been an increase in perennial weeds that are difficult to control with these chemicals, and improvement is desired. It is rare.

本発明者は、前記一般式(1)で表される化合物の除草
効果を増大させるべく研究を行った結果、一般式(1)
で表される化合物にMY−93を配合すると、それぞれ
の除草効果が単に相加的にえられるのみならず、相乗的
殺草効果が現れる事を見出し本発明を完成した。この相
乗効果は大きく本発明組成物により、イネに対して薬害
を及ぼずこともなく、低薬量でノビエ、−年生雑草から
多年生雑草まで完全に防除でき、本発明の有用性は非常
に大きい。また特にヒエに対する殺草効果の相乗作用は
著しく、上記の混合施用によって、本発明組成物中に含
まれるMY−93の使用薬量の低減をも可能とし、極め
て有用性が高い。
The present inventor conducted research to increase the herbicidal effect of the compound represented by the general formula (1), and found that the compound represented by the general formula (1)
The present invention was completed by discovering that when MY-93 is blended with the compound represented by the formula, the herbicidal effects of each compound are not only additive, but also a synergistic herbicidal effect appears. This synergistic effect is large, and the composition of the present invention does not cause any phytotoxicity to rice, and can completely control all types of weeds, from wild weeds to annual weeds to perennial weeds, with a low dosage, and the usefulness of the present invention is extremely large. . Furthermore, the synergistic herbicidal effect particularly on barnyard grass is remarkable, and by the above-mentioned mixed application, it is also possible to reduce the amount of MY-93 contained in the composition of the present invention, which is extremely useful.

また、本発明除草剤組成物は、雑草の発芽前および発芽
後に処理しても効果を有し、土壌処理、茎葉兼土壌処理
でも高い効果が得られる。又、イネ以外の各種穀類に対
しても有用であり、その他の畑地、果樹園などの農園芸
分野及び運動場、空き地、林地、タンクヤード、線路端
などの非農耕地における各種雑草の防除にも適用でき、
雑草防除にあたって大きな経済的効果を示す。
Furthermore, the herbicidal composition of the present invention is effective even when treated before and after weed germination, and is highly effective when treated with soil or with both foliage and soil. It is also useful for various grains other than rice, and can also be used to control various weeds in agricultural and horticultural fields such as fields and orchards, as well as in non-agricultural areas such as playgrounds, vacant lots, forest areas, tank yards, and railway edges. applicable,
Shows great economic effect in weed control.

本発明による組成物は、各成分の相対的活性にもよるが
、一般にはMY−93を1重量部当たり一般式(I>で
表される化合物0.001〜50重量部、好適には0.
001〜10重量部含んでいる。
Depending on the relative activity of each component, the composition according to the present invention generally contains 0.001 to 50 parts by weight of the compound represented by the general formula (I>) per 1 part by weight of MY-93, preferably 0. ..
001 to 10 parts by weight.

多くの場合、本発明の配合除草剤の最高の利点は式(1
)で表される化合物の割合がMY−93よりも比較的低
い時、例えばMY、−,93が0.001〜0.1重量
部のときに得られる。
In many cases, the greatest advantage of the combined herbicide of the present invention is that the formula (1
) is obtained when the proportion of the compound represented by is relatively lower than that of MY-93, for example, when MY, -,93 is 0.001 to 0.1 part by weight.

適用すべき混合物の量は、多数の因子、例えば生育を阻
止すべき特定の対象植物の種類などにより左右されるが
、一般に0.001〜10Kg/haの量が普通は適当
である。当業者であれば標準化された通常のテストによ
り特に多数の実験を行わなくても適当な使用割合が容易
に決定出来る。
The amount of mixture to be applied will depend on a number of factors, such as the particular species of target plant to be inhibited, but generally amounts of 0.001 to 10 Kg/ha are usually adequate. Those skilled in the art can readily determine appropriate usage rates by routine, standardized tests without the need for extensive experimentation.

本発明組成物は、活性成分を固体または液体希釈剤から
なるキャリヤーと混合した組成物の形態で使用するのが
好ましい。組成物は更に界面活性剤を含むのが好ましい
The compositions of the invention are preferably used in the form of a composition in which the active ingredient is mixed with a carrier consisting of a solid or liquid diluent. Preferably, the composition further comprises a surfactant.

次ぎに本発明における一般式(I)で表される化合物の
代表例を第1表に示す。以下の化合物は一般式(1)で
表される化合物に包含されるものではあるが、一般式(
1)で表される化合物はこれらに限定されるものではな
い。
Next, Table 1 shows representative examples of the compounds represented by the general formula (I) in the present invention. Although the following compounds are included in the compounds represented by the general formula (1), they are also included in the compounds represented by the general formula (1).
The compounds represented by 1) are not limited to these.

第1表 Me:メチル基 Et:エチル基 個々の活性化合物は、その除草活性にそれぞれ欠点を示
すi合が多くあるが、その場合2種の活性化合物を組合
せた場合の除草活性が、その2種の化合物の各々の活性
の単純な合計(期待される活性)よりも大きくなる場合
にこれを相乗4乍用とも1う。2種の除草剤の特定組合
せにより期待される活性は、次のようにして計算するこ
と力(できる。
Table 1 Me: Methyl group Et: Ethyl group There are many combinations in which individual active compounds exhibit drawbacks in their herbicidal activity, but in such cases, the herbicidal activity when two types of active compounds are combined is This is also called synergism when the activity is greater than the simple sum of the activities of each of the species (the expected activity). The expected activity of a particular combination of two herbicides can be calculated as follows.

(Colby S、R,除草剤の組合せの相乗及び拮抗
1乍用反応の計算rWeedJ 15620〜22頁、
1967年を参I!嘱)α:除草剤AをaKg/haの
量で処理した時の抑制率 β:除草剤BをbKg/haの量で処理した時の抑制率 E:除草剤AをaKg/ha、除草剤Bをbag/ha
の量で処理した場合に期待される抑制率即ち、実際の抑
制率が上記計算より太きtl)ならGヨ組合せによる活
性は相乗作用を示すとG)うこと力くできる。
(Colby S, R, Calculation of synergistic and antagonistic responses of herbicide combinations rWeedJ 15620-22,
Let's go back to 1967!嘱) α: Suppression rate when herbicide A is treated at a Kg/ha amount β: Suppression rate E when herbicide B is treated at bKg/ha: Herbicide A at a Kg/ha, herbicide B bag/ha
If the expected inhibition rate, that is, the actual inhibition rate when treated with the amount of tl), is thicker than the above calculation, it can be concluded that the activity by the combination of G) shows a synergistic effect.

以下本発明を実施例によりさらに具体的に説明するが、
本発明における化合物、製剤量、列形等(よ実施例のみ
に限定されるものではなし)。
Hereinafter, the present invention will be explained in more detail with reference to Examples.
Compounds, formulation amounts, series, etc. (not limited to examples only) in the present invention.

尚、「部」は全て重量部を意味する。In addition, all "parts" mean parts by weight.

化合物No6−−−−−0.07部 M Y−93−一一−−−−・ 8部 ベントナイト −−−−−〜−−−=−40部タルク 
−−−−−〜−−−−−−51.93部以上を均一に混
合粉砕して後少量の水を加えて攪拌混合捏和し、押し出
し式造粒機で造粒し、乾燥して粒剤にする。
Compound No. 6---0.07 part M Y-93-11----・8 parts bentonite--------=-40 parts talc
−−−−−−−−−−−− After uniformly mixing and pulverizing 51.93 parts or more, adding a small amount of water, stirring and kneading, granulating with an extrusion type granulator, and drying. Make into granules.

藍企皿主 粒剤 化合物No、 2 −−−−−− 0.2部MY−93
−−〜−−,−,10部 ベントナイト −−−−−−−−、50部タルク −−
−−−−−−−−−、39,8部以上を均一に混合粉砕
して後少量の水を加えて攪拌混合捏和し、押し出し式造
粒機で造粒し、乾燥して粒剤にする。
Aikitasu Granule Compound No. 2 ------- 0.2 parts MY-93
−−〜−−,−, 10 parts bentonite −−−−−−−, 50 parts talc −−
----------, 39.8 parts or more are uniformly mixed and pulverized, then a small amount of water is added, stirred and kneaded, granulated with an extrusion type granulator, and dried to form granules. Make it.

臥企但↓ 粒剤 化合物No、8 、 −−−−−− 0.1部M Y 
−93−−−−−10部 ベントナイト −−−−−−、40部 タルク −・−−−−−−−−−49,9部以上を均一
に混合粉砕して後少量の水を加えて攪拌混合捏和し、押
し出し式造粒機で造粒し、乾燥して粒剤にする。
Wokitan↓ Granule Compound No. 8, -------- 0.1 part MY
-93------10 parts bentonite----, 40 parts talc---49, 9 parts or more are uniformly mixed and ground, then a small amount of water is added. Stir, mix, and knead, granulate using an extrusion granulator, and dry to form granules.

配會皿土 水和剤 化合動歯5 −−−−−−−−−−− 0 、3部M 
Y −93−−−−−−−42部 ジ−クライト、a、 −一−−−−−−−−53,7部
(カオリン系クレー:ジークライト工業■商品名)ツル
ポール5039 ・−−一−−−−・・−2部(界面活
性剤:東邦化学■商品名) カープレックス(固結防止剤)−・−2部(ホワイトカ
ーボン:塩野義製薬■商品名)以上を均一に混合して水
和剤にする。
Distribution plate Hydrating agent compound moving tooth 5 ------------- 0, 3 parts M
Y -93---42 parts Zeekrite, a, -1---53,7 parts (Kaolin clay: Zeekrite Kogyo ■Product name) Tsurupol 5039 ・--1 --- 2 parts (surfactant: Toho Chemical ■trade name) Carplex (anti-caking agent) ---2 parts (white carbon: Shionogi & Co., Ltd. ■trade name) or more are mixed uniformly. and make it into a hydrating agent.

配イ1列」−水和剤 化合動歯7 −−−−−−−− 0.6部M Y −9
3−一一一一一−−−−−48部ジークライトA −−
−−−−−−−−−−47,4部(カオリン系クレー:
ジークライト工業■商品名)ツルポール5039 −−
−−−−−−一−−,2部(界面活性剤:東邦化学■商
品名) カープレックス(固結防止剤)−−−2部(ホワイトカ
ーボン:塩野義製薬■商品名)以上を均一に混合して水
和剤−にする。
Arrangement 1 row” - Hydrating agent compound movable tooth 7 ------- 0.6 part M Y -9
3-1111---48 part Sieglite A---
----------47,4 parts (kaolin clay:
Sieglite Industries ■Product name) Tsurupol 5039 --
−−−−−−1−−, 2 parts (surfactant: Toho Chemical ■trade name) Carplex (anticaking agent)---2 parts (white carbon: Shionogi & Co. ■trade name) or more uniformly to make a hydrating agent.

W↓ 湛水条件におりる除草効果試験 115000アールのワグネルボソト中に沖積土壌を入
れた後、水を入れて混和し水深2cmの淡水条件とする
。タイヌビエ、広葉雑草(コナギ、アゼナ、キカシグサ
)ホタルイのそれぞれの種子を、上記のポットに混播し
、さらにウリカワ、ミズガヤツリ、クログワイの塊茎を
置床した。さらに2.5葉期のイネ苗を移植した。ポッ
トを25〜30℃の温室内において植物を育成し、播種
後10日口重タイヌビエが1.5葉期の時期に水面へ所
定の薬量になるように、薬剤希釈液をメスピペットで滴
下処理した。薬液滴下後3週目に各種雑草に対する除草
効果を下記の判定基準に従って調査した。結果は第2表
及び第3表に示す。
W↓ Weeding effect test under flooded conditions After putting alluvial soil in a 115,000 are Wagner Bosoto, water is added and mixed to create a freshwater condition with a water depth of 2 cm. Seeds of Japanese grasshopper, broad-leaved weeds (Japanese chinensis, azalea, and Kikashigusa) were mixedly sown in the above-mentioned pots, and tubers of Japanese cypress, Japanese cypress, and black bream were also placed in the beds. Furthermore, rice seedlings at the 2.5 leaf stage were transplanted. Plants are grown in pots in a greenhouse at 25-30°C, and 10 days after sowing, when the Japanese millet is at the 1.5-leaf stage, a diluted drug solution is dripped onto the water surface using a measuring pipette at a predetermined dose. Processed. Three weeks after dropping the chemical solution, the herbicidal effect on various weeds was investigated according to the following criteria. The results are shown in Tables 2 and 3.

:v′:足基準 5− 殺草率 90%以上(はとんど完全枯死)4− 
殺草率 70〜89% 3− 殺草率 40〜69% 2− 殺草率 20〜39% 1− 殺草率 5〜19% 0−・−殺草率 5%以下(はとんど効力なし)但し、
上記の殺草率は、薬剤処理区の地上部生草重および無処
理区の地上部生草重を測定して下記の式によりめたもの
である。
:v': Foot standard 5- Weed killing rate 90% or more (almost completely dead) 4-
Weed killing rate 70-89% 3- Weed killing rate 40-69% 2- Weed killing rate 20-39% 1- Weed killing rate 5-19% 0--Weed killing rate 5% or less (mostly ineffective) However,
The above-mentioned weed killing rate was determined by the following formula by measuring the weight of above-ground plants in the chemically treated area and the weight of above-ground plants in the non-treated area.

以下余白 第2表 第2表(続き) 第3表 混合除草効果試験(殺草率2%) 第 3 表(続き) 試量■1 ヒエに対する相乗効果試験 内径8cmのポリエチレン製ポットに水田土壌を充填し
、水田状態でタイヌビエを育成し、ヒエの3葉期に粒剤
に製剤した各所定の薬〜剤を湛水土壌処理した。ポット
は25〜30℃の温室内に置い゛ζ管理育成し、処理後
30日回定残存しているヒエの地上部生草重及び無処理
区の地上部生草重を71111定し、殺草率を算出し下
記の判定基準に従って判定した。結果を第4表及び第5
表に示す。
Table 2 Table 2 (Continued) Table 3 Mixed herbicidal effect test (herbicidal rate 2%) Table 3 (Continued) Test amount ■1 Synergistic effect test on barnyard grass Filled with paddy soil in a polyethylene pot with an inner diameter of 8 cm Then, Japanese millet was grown in paddy fields, and the flooded soil was treated with each of the prescribed drugs formulated into granules at the third leaf stage of millet. The pots were placed in a greenhouse at 25 to 30°C for controlled cultivation, and the weight of remaining above-ground grass of barnyard grass in the untreated area was determined 30 days after treatment, and the weight of above-ground grass in the untreated area was determined. The grass rate was calculated and judged according to the following criteria. The results are shown in Tables 4 and 5.
Shown in the table.

評点 殺草率 0 0〜9% 1 10〜19% 2 20〜29% 3 30〜39% 4 40〜49% 5 50〜59% 6 60〜69% 7 70〜79% 8 80〜89% 9 90〜99% 10 100% 表中、計算値は前記Colbyの式よりめた期待値示す
Score Weed killing rate 0 0-9% 1 10-19% 2 20-29% 3 30-39% 4 40-49% 5 50-59% 6 60-69% 7 70-79% 8 80-89% 9 90 ~99% 10 100% In the table, the calculated values are the expected values calculated from the Colby equation.

以上の表から明らかなように、本発明組成物は、一般式
(I)で表される化合物及び従来公知の除草剤それぞれ
の活性の単純な合計にとどまらず、大きな相乗的除草活
性を有しており更にかつ低薬量で対象雑草を選択的に完
全に防除することごきる。
As is clear from the above table, the composition of the present invention has not only the simple sum of the activities of the compound represented by general formula (I) and the conventionally known herbicides, but also a large synergistic herbicidal activity. Furthermore, it is possible to selectively and completely control target weeds with a low dose.

特許出願人 日産化学工業株式会社Patent applicant: Nissan Chemical Industries, Ltd.

Claims (1)

【特許請求の範囲】 一般式(■): 〔式中へは低級アルキル基を示す。Bは水素原子または
低級アルキル基を示す。Rは低級アルキル基を示す。X
およびYはそれぞれ独立して、低級アルキル基または1
氏級アルコキシ基を示す。〕 で表されるピラゾールスルホニルウレア誘導体と5−(
1−メチル−1−フェネチル)−ピペリジン−1−カル
ボチオエート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。
[Claims] General formula (■): [In the formula, a lower alkyl group is shown. B represents a hydrogen atom or a lower alkyl group. R represents a lower alkyl group. X
and Y are each independently a lower alkyl group or 1
Indicates a grade alkoxy group. ] pyrazolesulfonylurea derivative represented by and 5-(
A herbicidal composition comprising 1-methyl-1-phenethyl)-piperidine-1-carbothioate as an active ingredient.
JP15394983A 1983-08-22 1983-08-22 Herbicidal composition Pending JPS6045505A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15394983A JPS6045505A (en) 1983-08-22 1983-08-22 Herbicidal composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15394983A JPS6045505A (en) 1983-08-22 1983-08-22 Herbicidal composition

Publications (1)

Publication Number Publication Date
JPS6045505A true JPS6045505A (en) 1985-03-12

Family

ID=15573592

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15394983A Pending JPS6045505A (en) 1983-08-22 1983-08-22 Herbicidal composition

Country Status (1)

Country Link
JP (1) JPS6045505A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1988002598A1 (en) * 1986-10-10 1988-04-21 E.I. Du Pont De Nemours And Company Herbicidal mixtures

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1988002598A1 (en) * 1986-10-10 1988-04-21 E.I. Du Pont De Nemours And Company Herbicidal mixtures

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