JPH04154705A - Herbicide for paddy rice plant having reduced phytotoxicity - Google Patents

Herbicide for paddy rice plant having reduced phytotoxicity

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Publication number
JPH04154705A
JPH04154705A JP27650390A JP27650390A JPH04154705A JP H04154705 A JPH04154705 A JP H04154705A JP 27650390 A JP27650390 A JP 27650390A JP 27650390 A JP27650390 A JP 27650390A JP H04154705 A JPH04154705 A JP H04154705A
Authority
JP
Japan
Prior art keywords
herbicide
compound
paddy rice
alpha
rice plant
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
JP27650390A
Other languages
Japanese (ja)
Inventor
Yuji Yamada
祐司 山田
Takashi Nishisaka
西坂 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.)
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 JP27650390A priority Critical patent/JPH04154705A/en
Publication of JPH04154705A publication Critical patent/JPH04154705A/en
Pending legal-status Critical Current

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  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE:To obtain a herbicide for paddy field having a little phytotoxicity and high effects by adding 1-(alpha,alpha-dimethylbenzyl)-3-p-tolylurea to S-benzyl-N-(1,2- dimethylpropyl)-N-ethylthiocarbamate. CONSTITUTION:1-(alpha,alpha-Dimethylbenzyl)-3-p-tolylurea is added to S-benzyl-N-(1,2- dimethylpropyl)-N-ethylthiocarbamate to give an extremely useful herbicide which enormously reduces phytotoxicity of the above-mentioned thiocarbamate to paddy rice plant and has enhanced effects on cockspur-grass and cyperaceous weeds.

Description

【発明の詳細な説明】 (1)産業上の利用分野 S−ベンジル−N −(1,2−ジメチルプロピル)−
N−エチルチオカーバメート(以下、化合物Aとする。
Detailed description of the invention (1) Industrial application field S-benzyl-N-(1,2-dimethylpropyl)-
N-ethylthiocarbamate (hereinafter referred to as compound A).

)と1− (α、α−ジメチルベンジル)−3−p−)
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の水稲への薬害か著しく軽減され
た水稲用除草剤に関するものである。
) and 1- (α,α-dimethylbenzyl)-3-p-)
The present invention relates to a herbicide for paddy rice that contains rillurea (hereinafter referred to as compound B) as an active ingredient and has significantly reduced chemical damage to paddy rice caused by compound A.

(2)従来の技術及び発明か解決しようとする問題点化
合物AはIOa当り、200g前後の薬量で水田の1年
少雑草、例えばノビエ、タマガヤツリ、コナギに高い効
力を示す除草剤として公知である。
(2) Prior Art and Problems to be Solved by the Invention Compound A is known as a herbicide that exhibits high efficacy against young weeds in paddy fields, such as field weeds, Japanese cypress, and grasshopper, at a dosage of around 200 g per IOa. .

しかしなから化合物Aは多年生雑草、例えばカヤツリグ
サ科のホタルイ、ミズガヤツリ、クログワイ等及びオモ
ダカ科のウリカワ、オモダカ等に対する効果は不充分で
、また時として水稲に対して薬害を与えることかある。
However, Compound A is insufficiently effective against perennial weeds, such as Cyperaceae, Cyperaceae, Cyperaceae, and Cyperaceae, and Omodakaceae, Urikawa, Omodaka, etc., and may sometimes cause phytotoxicity to paddy rice.

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、移植直後の苗においてはより一層強い
薬害をもたらす。
Particularly, under poor environmental conditions such as high temperatures, sandy soil, and leaky rice paddies, seedlings planted shallowly or immediately after transplanting are more susceptible to chemical damage.

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、移植水稲に薬害の心配がなく、また−年少及
び多年生雑草に高い効力を示す、実用上、非當に有益で
ある水[Il用除草剤を提供するものである。
The present invention provides a water herbicide which is extremely useful in practice, without worrying about chemical damage to transplanted paddy rice, and which is highly effective against young and perennial weeds.

(3)問題点を解決するための手段 本発明者は、化合物Aに化合物Bを加えることにより、
化合物への水稲に対する薬害を著しく軽減し、し7かも
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 problem By adding compound B to compound A, the present inventor has solved the problem.
Surprising new findings have been discovered that the compound significantly reduces the chemical damage caused to paddy rice, and also enhances its efficacy against Cyperaceae weeds.

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か化合物Aか50〜80[1g/ 
1.Daに対して化合物Bは15−500g/l、0a
であって更に望ましくは化合物Aか150−400g/
10aに対して化合物Bは30〜300g/1.oaで
ある。
The effective mixing range of the herbicide for paddy fields of the present invention is whether the amount used is 50 to 80 [1 g/
1. Compound B is 15-500g/l with respect to Da, 0a
More preferably, 150 to 400 g of compound A/
Compound B is 30-300g/1.10a. It is OA.

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
状水利剤、重合体物質中のマイクロカプセル等の各種剤
型にすることかできる。
The herbicide for paddy fields of the present invention can be formulated into various dosage forms such as emulsions, wettable powders, granules, flowables, granular irrigation agents, and microcapsules in polymeric substances by applying conventional formulation methods for agricultural chemical formulations. I can do something.

また、キカシグサ、アゼナ、ヘラオモダカ、などの−手
生広葉雑草及び多年生難防除雑草のウリカワ、オモダカ
、クログワイに対する効果を増強するため、ヘンスルフ
ロンメチル、ビラゾスルフロンエチル、ンノスルフロン
、N−(2−クロロイミダゾ〔1,2〜a〕ピリンン−
3−イルスルホニル)−N′−(4,6−シフトキン−
2−ピリミジニル)ウレア、ビラゾレート、ビラゾキン
フェン、ヘンゾフエナソプ等を加えることも可能である
In addition, in order to enhance the effect on broad-leaved weeds such as Kikashigusa, Azena, Helaomodaka, etc. and perennial difficult-to-control weeds such as Urikawa, Omodaka, and Kurogwai, hensulfuron-methyl, virazosulfuron-ethyl, nnosulfuron, N-(2-chloro imidazo[1,2~a]pirin-
3-ylsulfonyl)-N'-(4,6-shiftkin-
It is also possible to add urea (2-pyrimidinyl), virazolate, virazoquinfen, henzofenasop, etc.

更に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。
Furthermore, in order to expand the range of action, other herbicides, insecticides, fungicides, plant growth regulators, fertilizers, etc. may be mixed.

(4)実施例 次に代表的な剤型の実施例をあげるか、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.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A2B部、化合物B28部、クレー37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5696を含有する水和剤を得る。
Example 1 Hydration containing 5696 active ingredients was prepared by mixing and pulverizing 2 parts of wettable powder compound A2B, 28 parts of compound B, 37 parts of clay, 2 parts of white carbon, 2 parts of sodium lignin sulfonate, and 3 parts of sodium alkylnaphthalene sulfonate. get the agent.

実施例2 粒剤 化合物A7部、化合物87部、ベントナイト30部、タ
ルク52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、混練機て練ったあと、造粒機を通して造粒し
、次いて乾燥整粒して有効成分14%を含有する粒剤を
得る。
Example 2 7 parts of granule compound A, 87 parts of compound, 30 parts of bentonite, 52 parts of talc, 2 parts of sodium dodecylbenzenesulfonate and 2 parts of sodium ligninsulfonate were mixed, approximately 20 parts of water was added, and the mixture was mixed in a kneader. After kneading, the mixture is granulated through a granulator, and then dried and sized to obtain granules containing 14% of the active ingredient.

(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か示すように
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草効
力を増強しうるとともに、化合物Aの有する水稲に対す
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 later, the herbicide for rice fields of the present invention is capable of increasing the herbicidal efficacy of compound A against weeds and weeds of the Cyperaceae family by adding and using compound B in combination with compound A. In addition, it becomes possible to significantly reduce the phytotoxicity of Compound A to paddy rice.

試験例1 100ml三角フラスコに、ニスプロカルブを有効成分
として、1.3.2.6.5.2.10.41)pm、
ダイムロンを0.18.0.37.0.75.1.5.
 3 ppm及び、それぞれの薬剤を混合し、所定濃度
に調製した春日井氏水耕液100 mlを分注し、2葉
期の水稲(品種;コシヒカリ) 10本を、根部浸漬処
理した。
Test Example 1 In a 100 ml Erlenmeyer flask, Nisprocarb was added as an active ingredient at 1.3.2.6.5.2.10.41) pm,
Daimron 0.18.0.37.0.75.1.5.
100 ml of Mr. Kasugai's hydroponic solution prepared by mixing 3 ppm and each drug to a predetermined concentration was dispensed, and 10 paddy rice plants (variety: Koshihikari) at the two-leaf stage were subjected to root immersion treatment.

その後、三角フラスコは、アルミホイルで覆い、昼り0
℃/16時間(10,0001ux)、夜り5℃/8時
間の人工気象室内で生育させた。処理後10日目に、イ
ネの第3葉身長と第4葉身長をn1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
After that, cover the Erlenmeyer flask with aluminum foil and
It was grown in an artificial climate room at 5° C./8 hours at night at 16 hours (10,0001 ux). On the 10th day after the treatment, the height of the third leaf and the height of the fourth leaf of rice were determined as n1, 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 1/ 5000 aのワグネルポットに水田土壌をつめ
代かきを行い湛水法を4cmとした。ウリカワ、クログ
ワイの塊茎を3cmの深度に埋め込んだ後、ノビエ、ホ
タルイを土中1(至)に混播、タマガヤツリ、コナギ、
ミズガヤツリ塊茎を土壌表面に播種し、翌日、2葉期の
イネ(品種、コシヒカリ)をポット当り6個体(1叩植
3個体、3cITl植3個体)を移植した。移植後7日
目に実施例2に準じて調整した粒剤を水面処理し、処理
翌日及び翌々日に3cm/日の漏水操作を行った。処理
後20日目に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t
二。
Test Example 2 Paddy soil was plowed into a 1/5000 a Wagner pot and the flooding method was set to 4 cm. After burying the tubers of Urikawa and Kurogwai to a depth of 3 cm, mixed sowing of Nobie and Hotarui in the soil 1 (towards the bottom), Tamaga yatsuri, Konagi,
Cyperus tubers were sown on the soil surface, and on the next day, 6 individuals of two-leaf stage rice (variety: Koshihikari) were transplanted per pot (3 individuals per pound, 3 individuals planted in 3cITl). Seven days after transplantation, the water surface was treated with the granules prepared according to Example 2, and water leakage was performed at a rate of 3 cm/day the day after the treatment and the day after. On the 20th day after the treatment, observation and investigation were conducted according to the following criteria. In addition, regarding rice chemical damage, observational evaluation and plant height measurements were made, and plant height was expressed as a ratio to untreated plots. The results are shown in Table 2.
two.

0 効果薬害なし〜jO:完全枯死 表    1 表  ]   (続き)0 Effect No chemical damage~jO: Complete withering Table 1 Table       (Continued)

Claims (1)

【特許請求の範囲】[Claims] S−ベンジル−N−(1,2−ジメチルプロピル)−N
−エチルチオカーバメートと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。
S-benzyl-N-(1,2-dimethylpropyl)-N
- A herbicide for paddy rice with reduced phytotoxicity, characterized by containing ethylthiocarbamate and 1-(α,α-dimethylbenzyl)-3-p-tolylurea as active ingredients.
JP27650390A 1990-10-17 1990-10-17 Herbicide for paddy rice plant having reduced phytotoxicity Pending JPH04154705A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP27650390A JPH04154705A (en) 1990-10-17 1990-10-17 Herbicide for paddy rice plant having reduced phytotoxicity

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP27650390A JPH04154705A (en) 1990-10-17 1990-10-17 Herbicide for paddy rice plant having reduced phytotoxicity

Publications (1)

Publication Number Publication Date
JPH04154705A true JPH04154705A (en) 1992-05-27

Family

ID=17570372

Family Applications (1)

Application Number Title Priority Date Filing Date
JP27650390A Pending JPH04154705A (en) 1990-10-17 1990-10-17 Herbicide for paddy rice plant having reduced phytotoxicity

Country Status (1)

Country Link
JP (1) JPH04154705A (en)

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