JPH02258704A - Herbicide for paddy rice reduced in phytotoxicity - Google Patents

Herbicide for paddy rice reduced in phytotoxicity

Info

Publication number
JPH02258704A
JPH02258704A JP7797589A JP7797589A JPH02258704A JP H02258704 A JPH02258704 A JP H02258704A JP 7797589 A JP7797589 A JP 7797589A JP 7797589 A JP7797589 A JP 7797589A JP H02258704 A JPH02258704 A JP H02258704A
Authority
JP
Japan
Prior art keywords
compound
herbicide
phytotoxicity
alpha
paddy rice
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
JP7797589A
Other languages
Japanese (ja)
Other versions
JP2750533B2 (en
Inventor
Takashi Nishisaka
西坂 隆
Hiroshi Koyanagi
小柳 弘
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.)
SDS Biotech Corp
Original Assignee
SDS Biotech 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 SDS Biotech Corp filed Critical SDS Biotech Corp
Priority to JP7797589A priority Critical patent/JP2750533B2/en
Publication of JPH02258704A publication Critical patent/JPH02258704A/en
Application granted granted Critical
Publication of JP2750533B2 publication Critical patent/JP2750533B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To obtain the title herbicide containing 3-(4,6-dimethoxy-1,3,5-triazin-2- yl)-1-[2-(2-methoxyethoxy)-phenylsulfonyl]urea and 1-(alpha,alpha-dimethylbenzyl)-3-p- tolylurea. CONSTITUTION:The title herbicide containing 3-(4,6-dimethoxy-1,3,5triazin-2- yl)-1-[2-(2-methoxyethoxy)phenylsulfonyl]urea (A) and 1-(alpha,alpha-dimethylbenzyl)-3-p- tolylurea (B) as active ingredients. Although the compound A exhibits high weeding effect on weed in paddy field at low chemical amount and sometimes gives phytotoxicity to paddy rice on other hand, a herbicide remarkably reduced in phytotoxicity to transplanted and directly seeded paddy rice and capable of exhibiting high effect on annual weed and perennial weed can be obtained by using the compound A together with the compound B. Amounts of the compound A and compound B used are each 1-10g and 30-100g per 10a.

Description

【発明の詳細な説明】 (1)  産業上の利用分野 本発明は3− (4J−ジメトキシ−1,3,5−hリ
アジン−2−イル)−1−C2−(2−メトキシエトキ
シ)−フェニルスルホニル〕尿素(以下、化合物Aとす
る。)と1− (α、α−ジメチルベンジル)−3−p
−トリル尿素(以下、化合物Bとする。)とを有効成分
として含有する、化合物Aの水稲への薬害が著しく軽減
された水稲用除草剤に関するものである。
Detailed Description of the Invention (1) Industrial Field of Application The present invention is directed to 3-(4J-dimethoxy-1,3,5-h riazin-2-yl)-1-C2-(2-methoxyethoxy)- phenylsulfonyl]urea (hereinafter referred to as compound A) and 1-(α,α-dimethylbenzyl)-3-p
- Tolylurea (hereinafter referred to as Compound B) as an active ingredient, the herbicide for paddy rice has significantly reduced phytotoxicity of Compound A to paddy rice.

(2)従来の技術及び発明が解決しようとする問題点化
合物Aは従来の除草剤の1/100〜l/ 200とい
う低薬量で、ノビエを除く一年生雑草、例えばタマガヤ
ツリ、コナギ、ヒメミソハギ等、及び多年生雑草例えば
マツバイ、ウリカワ、オモダカ等の水田雑草に高い除草
効果を示す除草剤として公知である。
(2) Problems to be solved by the conventional technology and the invention Compound A is used in a low dosage of 1/100 to 1/200 of conventional herbicides, and is effective against annual weeds other than weeds, such as cyperus japonica, japonica japonica, and japonica japonica, etc. It is also known as a herbicide that exhibits a high herbicidal effect on perennial weeds such as paddy field weeds, such as Japanese grasshopper, paddy field weeds, and paddy field weeds.

しかしながら化合物Aは時として水稲に対して薬害を与
えることがある。特に、高温、砂質土壌、漏水田等の不
良環境条件下においてまた浅植苗、移植または播種直後
の苗においてはより一層強い薬害をもたらす。
However, Compound A sometimes causes phytotoxicity to paddy rice. Particularly, under poor environmental conditions such as high temperatures, sandy soil, and leaky rice fields, and in shallowly planted seedlings, seedlings immediately after transplanting, or seedlings, it causes even stronger phytotoxicity.

一方、化合物Bは除草剤としては公知であり水田のノビ
エ及びカヤツリグサ科雑草のタマガヤツリ、ホタルイ、
マツバイ、ミズガヤツリ、クログワイ等に優れた除草効
果を示すため、これらの雑草の除草剤として広く普及し
ている。
On the other hand, Compound B is known as a herbicide, and is used to control rice field weeds and Cyperaceae weeds such as Cyperus and Firefly.
It is widely used as a herbicide for weeds such as Japanese grasshopper, Japanese cypress, and black croaker, as it shows excellent herbicidal effects on these weeds.

これまで化合物Aと化合物Bの併用について、記載した
文献はない。
Until now, there is no literature describing the combination of Compound A and Compound B.

本発明は、移植及び1α播水稲に薬害の心配がなく、ま
た−年少及び多年生雑草全般に高い効力を示す、実用上
、非常に有益である水田用除草剤を提供するものである
The present invention provides a practically very useful herbicide for paddy fields that is free from chemical damage to transplanted and 1α-seeded rice, and exhibits high efficacy against young and perennial weeds in general.

(3)問題点を解決するための手段 本発明者らは、化合物Aに化合物Bを加えることにより
、化合物Aの水稲に対する薬害を著しく軽減し、しかも
ノビエおよびカヤツリグサ科雑草に対する効力を増強す
るという驚くべき、新知見を見い出した。
(3) Means for Solving the Problems The present inventors have found that by adding Compound B to Compound A, the phytotoxicity of Compound A to paddy rice can be significantly reduced, and the efficacy against field weeds and Cyperaceae weeds can be enhanced. I discovered surprising new knowledge.

本発明の水田用除草剤の配合量について有効な混合範囲
を示せばその使用量が化合物Aが0,5〜2Of/IO
aに対して化合物Bは15〜500 g / 10 a
であって更に望ましくは化合物Aが1〜10g/10a
に対(2て化合物Bは30〜300 g/ 10 aで
ある。
The effective mixing range of the herbicide for paddy fields of the present invention is that the amount of compound A used is 0.5 to 2 Of/IO.
Compound B is 15-500 g/10 a for a
More preferably, the amount of compound A is 1 to 10 g/10a
(2) Compound B is 30-300 g/10 a.

本発明の水田用除草剤は農薬製剤上慣用の製剤化方法を
応用して例えば乳剤、水和剤、粒剤、フロワブル、顆粒
状水和剤、重合体物質中のマイクロカプセル等の各種剤
型にすることができる。
The herbicide for paddy fields of the present invention can be formulated into various dosage forms such as emulsions, wettable powders, granules, flowables, granular wettable powders, and microcapsules in polymeric substances by applying conventional formulation methods for agricultural chemical formulations. It can be done.

また作用の範囲を拡大するために、他の除草剤、殺虫剤
、殺菌剤あるいは植物生長調節剤、肥料等を混合するこ
ともできる。
Further, in order to expand the range of action, other herbicides, insecticides, fungicides, plant growth regulators, fertilizers, etc. can be mixed.

(4)実施例 次に代表的な剤型の実施例をあげるが、有効成分の混合
比は前述の範囲で変更し得ることはいうまでもない。説
明文中“部”は重量部を示す。
(4) Examples Next, examples of typical dosage forms will be given, but it goes without saying that the mixing ratio of the active ingredients can be varied within the above-mentioned range. "Parts" in the description indicate parts by weight.

実施例1 水和剤 化合物A3部、化合物880部、ケイソウ上10部、ク
レー20部、ホワイトカーボン2部、リグニンスルホン
酸ソーダ2部及びアルキルナフタレンスルホン酸ソーダ
3部を混合粉砕して有効成分6326を含有する水和剤
を得る。
Example 1 3 parts of wettable powder compound A, 880 parts of compound, 10 parts of diatomaceous powder, 20 parts of clay, 2 parts of white carbon, 2 parts of sodium ligninsulfonate, and 3 parts of sodium alkylnaphthalenesulfonate were mixed and ground to obtain active ingredient 6326. A hydrating agent containing the following is obtained.

実施例2 粒剤 化合物A0.15部、化合物83部、ベントナイト25
部、タルク 8’!、85部、ドデシルベンゼンスルホ
ン酸ソーダ2部及びリグニンスルホン酸ソーダ2部を混
和し、水約20部を加えて、混練機で練ったあと、造粒
機を通して造粒し、次いで乾燥整粒して有効成分3.1
5%を含有する粒剤を得る。
Example 2 Granule Compound A 0.15 parts, Compound 83 parts, Bentonite 25
Department, talc 8'! , 85 parts of sodium dodecylbenzenesulfonate, 2 parts of sodium dodecylbenzenesulfonate, and 2 parts of sodium ligninsulfonate were mixed together, about 20 parts of water was added, and the mixture was kneaded in a kneader, then granulated through a granulator, and then dried and sized. Active ingredient 3.1
Granules containing 5% are obtained.

(5)発明の効果および試験例 本発明の水田用除草剤は後記した試験結果が示すように
化合物Aに化合物Bを添加、併用することにより、化合
物Aのノビエおよびカヤツリグサ科雑草に対する除!:
i効力を増強しつるとともに、化合物Aのをする水稲に
対する薬害を著しく軽減しうるようになる。
(5) Effects of the invention and test examples As shown in the test results described below, the herbicide for paddy fields of the present invention is effective against compound A and weeds of the Cyperaceae family by adding and using compound B in combination with compound A. :
In addition to increasing the potency of compound A, the chemical damage to paddy rice grown by compound A can be significantly reduced.

試験例1 1Hcシのプラスチックポットに、代かきした水田土壌
をつめ、2葉期のイネ(品種、初産)をポット当り10
個体1印の植付深度に移植した。移植翌日3cm湛水と
し実施例1に阜じて調整した水和剤所定薬量になる様に
水で希釈し田面水に滴下l、た。その後ポットは昼り0
℃/16時間(1口、0001ux)、夜り5℃/8時
間の人工気象室内で生育させた。処理後6日月に、イネ
の第3葉身長を測定し、対無処理区比を求めた。尚実験
は2反復で行い、結果は表1に示した。
Test Example 1 A 1Hc plastic pot was filled with paddy soil, and 10 rice plants (variety, first production) at the two-leaf stage were placed in each pot.
It was transplanted to the planting depth of individual 1 mark. The next day after transplantation, the hydrating powder prepared according to Example 1 was submerged with water to a depth of 3 cm, diluted with water to a predetermined dose, and dropped into rice field water. After that, the pot is 0 at noon.
It was grown in an artificial climate room at 5° C./8 hours at night (1 mouth, 0001 ux) for 16 hours at 5°C. Six days after the treatment, the height of the third leaf of rice was measured, and the ratio to the untreated plot was determined. The experiment was repeated twice, and the results are shown in Table 1.

試験例2 115000aのワグネルボットに水田土壌をつめ代か
きを行い湛水法を4cmとした。ノビエ、コナギ、ヒメ
ミソハギ、ホタルイの種子を播種し、オモダカ、ウリカ
ワ、ミズガヤツリ、クログワイの塊茎を埋め込み、2葉
期のイネ(品種、初産)をポット当り6個体(1cm?
1¥3個体、3c+n植3個体)を移植した。移植後1
1日エト実施例2に弗じて調整した粒剤を水面施用した
。処理翌日及び翌々I]に3−7口の漏水操作を行った
。処理後32日ロー以下の基準に従い観察調査を行った
。またイネ薬害については観察評価と草丈、差数を測定
し草丈については対無処理区比の値で表わした。結果は
表2に示した。
Test Example 2 Paddy soil was plowed into a 115,000a Wagnerbot, and the flooding method was set to 4 cm. Seeds of Novie, Konagi, Hyememisohagi, and Hotarui were sown, and tubers of Omodaka, Urikawa, Mizugayatsu, and Kurogwai were sown, and two-leaf stage rice (variety, first production) were planted, 6 individuals per pot (1cm?
1\3 individuals, 3c+n 3 individuals) were transplanted. After transplant 1
The granules prepared in Example 2 were applied to the water surface for one day. On the day after the treatment and the day after that, water leakage operations were performed at 3 to 7 ports. Observation and investigation were conducted 32 days after treatment according to the following criteria. In addition, regarding rice chemical damage, observational evaluation, plant height, and number of differences were measured, and plant height was expressed as the value of the ratio to the untreated plot. The results are shown in Table 2.

0:効果薬害なし〜10:完全貼死0: No effect, no drug damage ~ 10: Completely dead

Claims (1)

【特許請求の範囲】 1、3−(4,6−ジメトキシ−1,3,5−トリアジ
ン−2−イル)−1−〔2−(2−メトキシエトキシ)
−フェニルスルホニル〕尿素と1−(α,α−ジメチル
ベンジル)−3−p−トリル尿素を有効成分として含有
することを特徴とする薬害が軽減された水稲用除草剤。
[Claims] 1,3-(4,6-dimethoxy-1,3,5-triazin-2-yl)-1-[2-(2-methoxyethoxy)
-Phenylsulfonyl]urea and 1-(α,α-dimethylbenzyl)-3-p-tolylurea as active ingredients.A herbicide for paddy rice with reduced phytotoxicity.
JP7797589A 1989-03-31 1989-03-31 Rice herbicide with reduced phytotoxicity Expired - Lifetime JP2750533B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7797589A JP2750533B2 (en) 1989-03-31 1989-03-31 Rice herbicide with reduced phytotoxicity

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7797589A JP2750533B2 (en) 1989-03-31 1989-03-31 Rice herbicide with reduced phytotoxicity

Publications (2)

Publication Number Publication Date
JPH02258704A true JPH02258704A (en) 1990-10-19
JP2750533B2 JP2750533B2 (en) 1998-05-13

Family

ID=13648898

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7797589A Expired - Lifetime JP2750533B2 (en) 1989-03-31 1989-03-31 Rice herbicide with reduced phytotoxicity

Country Status (1)

Country Link
JP (1) JP2750533B2 (en)

Also Published As

Publication number Publication date
JP2750533B2 (en) 1998-05-13

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