JPS6045503A - Herbicide - Google Patents

Herbicide

Info

Publication number
JPS6045503A
JPS6045503A JP15394783A JP15394783A JPS6045503A JP S6045503 A JPS6045503 A JP S6045503A JP 15394783 A JP15394783 A JP 15394783A JP 15394783 A JP15394783 A JP 15394783A JP S6045503 A JPS6045503 A JP S6045503A
Authority
JP
Japan
Prior art keywords
parts
lower alkyl
herbicide
oxadiazon
formula
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
JP15394783A
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 JP15394783A priority Critical patent/JPS6045503A/en
Publication of JPS6045503A publication Critical patent/JPS6045503A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:A herbicide capable of controlling completely Echinochloa crus-galli Beauv. var. praticola Ohwi., annual and perennial weeds with its small amount without providing paddy rice plants with phytotoxicity, containing a pyrazolesulfonylurea derivative and oxadiazon as active ingredients. CONSTITUTION:A herbicide containing 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) and 3-(2,4-dichloro-5-isopropoxyphenyl)-5-t- butyl-1,3,4-oxadiazol-2(3H)-one (oxadiazon for short) as active ingredients. The ratio of the composition contained is sually 0.001-50pts.wt., preferably 0.001- 10pts.wt. compound shown by the formula based on 1pt.wt. oxadiazon.

Description

【発明の詳細な説明】 本発明は一般式(■): 〔式中^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ホニルウレア誘導体と3−(
2,4−ジクロロ−5−イソプロポキシフェニル)−5
−t−ブチル−1,3,4−オキサジアゾール−2(3
H)−オン(以下オキサシアシンと称する。)とを有効
成分として含有することを特徴とする除草剤に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention is based on the general formula (■): [In the formula, ^ 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. ] pyrazolesulfonylurea derivative represented by and 3-(
2,4-dichloro-5-isopropoxyphenyl)-5
-t-butyl-1,3,4-oxadiazole-2(3
The present invention relates to a herbicide containing H)-one (hereinafter referred to as oxacyacin) 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、−平生
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 grass-like grass and perennial broad-leaved weeds, but also against perennial weeds, making it highly useful.

また従来より知られている、オキサシアシンはノビエ、
−年生雑草、ホタルイに対し、一般式(I]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。
Oxacyacin, which has been known for a long time, is found in wild animals,
- Higher doses of compounds represented by formula (I) have been used against annual weeds and firefly, resulting in an increase in perennial weeds that are difficult to control with these chemicals;
Improvement is desired.

本発明者は、前記一般式(I)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(I)
で表される化合物に、従来使用されているオキサシアシ
ンを配合すると、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すこともなく、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オキサシアシンの使用
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 (I), and found that the compound represented by the general formula (I)
We have completed the present invention by discovering that when the compound represented by the formula is blended with the conventionally used oxacyacin, the herbicidal effects of each compound are not merely additive, but also a synergistic herbicidal effect appears. This synergistic effect is great, and the composition of the present invention does not cause any phytotoxicity to rice, and can completely control everything from wild weeds, 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 possible to reduce the amount of oxacyacin 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
、一般にはオキサシフフッ1重量部当たり一般式(+)
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。
Compositions according to the present invention generally contain a compound having the general formula
0.001 to 50 parts by weight, preferably 0.001 to 50 parts by weight of the compound represented by
.. 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(I
)で表される化合物の割合がオキサシアシンよりも比較
的低い時、例えば他の除草剤1重量部当たり一般式CI
)で表される化合物が0.001〜0.1重量部のとき
に得られる。
In many cases, the greatest advantage of the combined herbicides of the present invention is the formula (I
) is relatively lower than that of oxacyacin, for example, when the proportion of compounds of the general formula CI per part by weight of the other herbicide is
) is obtained when the amount of the compound represented by 0.001 to 0.1 part by weight 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(1)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 compound represented by the general formula (1) 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.

以下余白 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
す場合が多くあるが、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
にこれを相乗作用という。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が
できる。
Table 1 in the margin below Me: Methyl group Et: Ethyl group Individual active compounds often exhibit drawbacks in their herbicidal activity, but in such cases, the herbicidal activity when two types of active compounds are combined is When the activity of two compounds is greater than the simple sum of their respective activities (expected activity), this is called synergism. 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
作用反応の計算rWeedJ 15巻20〜22頁、1
967年を参照)00 α:除草剤AをaKg/haO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bKg/ha
O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大きいならば組合せによる活性は相
乗作用を示すということができる。
(Colby S, R, Calculation of synergistic and antagonistic responses of herbicide combinations rWeedJ vol. 15, pp. 20-22, 1
967) 00 α: Inhibition rate β when herbicide A is treated at an amount of aKg/haO: Inhibition rate E when herbicide B is treated at an amount of bKg/ha: Herbicide A is aKg/ha , herbicide B bKg/ha
If the expected inhibition rate when treated with the amount of O, that is, the actual inhibition rate is greater than the above calculation, it can be said that the combined activity exhibits 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、列形等は実施例のみ
に限定されるものではない。
Hereinafter, the present invention will be explained in more detail with reference to Examples.
The compounds, formulation amounts, array types, etc. in the present invention are not limited to the examples.

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

記名■1 粒剤 化合物NO,6、−−−−−−−−0,2部オキサシア
シン −−−−−−−−−1,0部ヘントナイト −−
−−−−−−−−−50部タルク −−一−−−・−・
−−−−−−48、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7粒剤にする。
Name ■1 Granule Compound No. 6, -------0,2 parts Oxacyacin ---1,0 parts Hentonite ---
−−−−−−−−−50 parts talc −−1−−−・−・
------- 48, 8 parts or more are uniformly mixed and pulverized, then a small amount of water is added, stirred and kneaded, granulated with an extrusion granulator, and dried to form 7 granules.

【企皿l 粒剤 化合物歯8 −−−−−−−−− 0.1部モリネート
 −−−−−・−0,7部 ベントナイト −−−−−−40部 タルク −−−−−,−−59、2部 以」二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。
[Planning plate l Granule compound tooth 8 ----------- 0.1 part Molinate ------0.7 parts Bentonite ------40 parts Talc ---, --59, 2 parts or more - After uniformly mixing and pulverizing 2 parts, adding a small amount of water, stirring and kneading, granulating with an extrusion type granulator, and drying to form granules.

配合耐重 水和剤 化合物阻4 −・−−−−−−−−−−−3部オキサシ
アシン −・−−−−−−−−−−−50部ジークライ
トA −−−−−−−−−43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 −−
−−−−・−、−−−、2部(非イオン性界面活性剤と
アニオン性界面活性剤との混合物: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)以上を均一に混合粉砕し
て水和剤とする。
Compound resistance Wettable powder Compound 4 -・-------------3 parts Oxacyacin ---50 parts Siegrite A --- -43 parts (kaolin clay:
Sieglite Industries ■Product name) Tsurupol 5039 --
-----・-, ---, 2 parts (mixture of nonionic surfactant and anionic surfactant: Toho Chemical ■ trade name) Carplex (anti-caking agent) --- 2 parts ( White carbon (Shionogi & Co., Ltd. trade name) is mixed and pulverized uniformly to make a wettable powder.

L金側(水和剤 化合物歯2 −−〜−−−−−−−−0 、 6部オキ
サシアシン −一−−−〜−−−−−−−9、0l?I
Iジ−クライトA 、−−−−=−−−86,4部(カ
オリン系クレー;ジークライト工業a1商品名)ツルポ
ール5039 −−−−〜−−−−−−−−−− 2部
(非イオン性界面活性剤とアニオン性界面活性剤との混
合物;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01商品名)以上を均一に混合粉砕し
て水和剤とする。
L gold side (wettable powder compound tooth 2 ----~----------0, 6 parts oxacyacin -1-----9, 0l?I
I Zeekrite A, -----=----86, 4 parts (kaolin clay; Zeekrite Kogyo A1 trade name) Tsurupol 5039 -------------- 2 parts ( Mixture of nonionic surfactant and anionic surfactant; Toho Chemical (trade name) Carplex (anti-caking agent) - 2 parts or more (white carbon: Shionogi & Co., Ltd. 01 brand name) are mixed and pulverized uniformly. and use it as a hydrating agent.

6担 フロアブル 化合物No、 3 −−−−−−−−0 、 3部オキ
サシアシン −−−−−−−−8部アグリヅールS−7
10 −−−−−10部(非イオン性界面活性剤:花王
アトラス■商品名) ルノソクス1000 C−’−−−−− 0 、 5部
(アニオン性界面活性剤:東邦化学■商品名)1%ロド
ポール水 −−−−−−−−−−−−20部(増粘剤:
ローン・ブーラン社商品名)水 −−−一−−−−−−
−−−−−−−−−−−−−−−−−m−−・−−−−
61、2部以上を均一に混合してフロアブル剤とする:
配合ロ旦 フロアブル 化合物N15 −−−−−−−−0.6部オキサシアシ
ン −−−−−−−−8部アゲリシールS’−710−
−−一−−10部(非イオン性界面活性剤:花王アトラ
ス側商品名) ルノノクス1000 C−−−−−−−−0、5部(ア
ニオン性界面活性剤:東邦化学側商品名)1%ロドポー
ル水 −−−一−−−−−−−−−−−−−20部(増
粘剤:ローン・ブーラン社商品名)水 −−−−−−−
−−−−−−−−−−−−−−60、9部以上を均一に
混合してフロアブル剤とする。
6 parts Flowable compound No., 3 ----------0, 3 parts oxacyacin - 8 parts Agridur S-7
10 ------- 10 parts (Nonionic surfactant: Kao Atlas ■Product name) Lunosox 1000 C-'------ 0, 5 parts (Anionic surfactant: Toho Chemical ■Product name) 1 % Rhodopol water -------------20 parts (thickener:
Lone Boulin product name) Water −−−1−−−−−−
−−−−−−−−−−−−−−−−−m−−・−−−−
61. Mix 2 or more parts uniformly to make a flowable agent:
Compounding compound Flowable compound N15 ----------0.6 parts Oxacyacin -8 parts Agelisil S'-710-
---10 parts (Nonionic surfactant: Kao Atlas brand name) Lunonox 1000 C---0, 5 parts (Anionic surfactant: Toho Chemical brand name) 1 % Rhodopol water --- 1--------20 parts (thickener: Lone-Boulin brand name) Water ---
-------------60.9 parts or more are uniformly mixed to form a flowable agent.

成駿(社)上 湛水条件における除草効果試験1150
00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°C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。
Narishun Co., Ltd. Herbicidal effect test under flooded conditions 1150
After putting alluvial soil in Wagner Bosoto of 00 ares,
Add water and mix to create freshwater conditions at a 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. 25 pots
Plants were grown in a greenhouse at ~30°C, and 10
At the 1.5-leaf stage of Japanese millet, a diluted drug solution was dropped onto the water surface using a volumetric pipette in a predetermined amount. 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.

判定基準 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% 〇 −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。
Judgment Criteria 5- Weed killing rate 90% or more (almost complete death) 4-
Weed killing rate 70-89% 3- Weed killing rate 40-69% 2 - Weed killing rate 20-39% 1- Weed killing rate 5-19% 〇 - Weed killing rate 5% or less (mostly not effective) However, the above The 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.

第2表 第2表(続き) 以下余白 第3表 試験■(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℃の温室内に置いて管理育成し、処理後30
日口重残存しているヒエの地上部生草重及び無処理区の
地上部生草重を測定し、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) Margin below Table 3 Test ■ (Synergistic effect test on millet Each prescribed drug was treated with flooded soil.The pots were placed in a greenhouse at 25 to 30°C for management and cultivation, and 30 minutes after treatment.
The above-ground fresh grass weight of the barnyard grass remaining in the daily harvest and the above-ground fresh grass weight of the untreated area were measured, and the weed killing rate was calculated and judged according to the following criteria. The results are shown in Tables 4 and 5.

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% 第4表 第4表(続き) 第5表 混合除草効果試験(殺草率1%) 第 5 表(続き) 表中、計算値は前記Co1byの式よりめた期待値を示
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% Table 4 Table 4 (continued) Table 5 Mixed herbicidal effect test (weed killing rate 1%) Table 5 (continued) In the table, the calculated values are the expected values calculated from the Co1by formula above. show.

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
の活性の単純な合羽にとどまらず、より大きな相乗的除
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ができる。
As is clear from the above table, the composition of the present invention does not merely combine the activities of the compound represented by general formula (I) and the conventionally known herbicides, but also has greater synergistic herbicidal activity. Furthermore, it is possible to selectively and completely control target weeds with a low dosage.

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(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ホニルウレア誘導体と3−(
2,4−ジクロロ−5−イソプロポキシフェニル)−5
−t−ブチル−1,3,4−オキサジアゾール−2(3
H)−オンとを有効成分として含有することを特徴とす
る除草剤。
[Claims] 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. ] pyrazolesulfonylurea derivative represented by and 3-(
2,4-dichloro-5-isopropoxyphenyl)-5
-t-butyl-1,3,4-oxadiazole-2(3
A herbicide characterized by containing H)-one as an active ingredient.
JP15394783A 1983-08-22 1983-08-22 Herbicide Pending JPS6045503A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15394783A JPS6045503A (en) 1983-08-22 1983-08-22 Herbicide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15394783A JPS6045503A (en) 1983-08-22 1983-08-22 Herbicide

Publications (1)

Publication Number Publication Date
JPS6045503A true JPS6045503A (en) 1985-03-12

Family

ID=15573552

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15394783A Pending JPS6045503A (en) 1983-08-22 1983-08-22 Herbicide

Country Status (1)

Country Link
JP (1) JPS6045503A (en)

Cited By (5)

* 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
JPH0834702A (en) * 1994-07-25 1996-02-06 Nissan Chem Ind Ltd Solid agrochemical composition
WO2000060944A1 (en) * 1999-04-13 2000-10-19 Aventis Cropscience S.A. Herbicidal compositions for paddy fields
JP2004510374A (en) * 2000-09-27 2004-04-02 レインジスター ワイアレス、インコーポレイテッド Omnidirectional antenna with multiple polarizations
JP2008288770A (en) * 2007-05-16 2008-11-27 Mitsubishi Electric Corp Ebg material

Cited By (7)

* 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
JPH0834702A (en) * 1994-07-25 1996-02-06 Nissan Chem Ind Ltd Solid agrochemical composition
WO2000060944A1 (en) * 1999-04-13 2000-10-19 Aventis Cropscience S.A. Herbicidal compositions for paddy fields
JP2002541163A (en) * 1999-04-13 2002-12-03 アベンティス クロップサイエンス ソシエテ アノニム Paddy field herbicide composition
JP4750949B2 (en) * 1999-04-13 2011-08-17 バイエル・エス・アー・エス Herbicide composition for paddy field
JP2004510374A (en) * 2000-09-27 2004-04-02 レインジスター ワイアレス、インコーポレイテッド Omnidirectional antenna with multiple polarizations
JP2008288770A (en) * 2007-05-16 2008-11-27 Mitsubishi Electric Corp Ebg material

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