JPS61109701A - Imidazole based herbicide - Google Patents

Imidazole based herbicide

Info

Publication number
JPS61109701A
JPS61109701A JP23218784A JP23218784A JPS61109701A JP S61109701 A JPS61109701 A JP S61109701A JP 23218784 A JP23218784 A JP 23218784A JP 23218784 A JP23218784 A JP 23218784A JP S61109701 A JPS61109701 A JP S61109701A
Authority
JP
Japan
Prior art keywords
herbicide
weeds
treatment
active ingredient
soil
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
JP23218784A
Other languages
Japanese (ja)
Other versions
JPH0510323B2 (en
Inventor
Hiroshi Kimoto
木本 博
Shozo Fujii
省造 藤井
Hiroshige Muramatsu
村松 廣重
Naonori Hirata
直則 平田
Hiromichi Oshio
大塩 裕陸
Katsuzo Kamoshita
鴨下 克三
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.)
National Institute of Advanced Industrial Science and Technology AIST
Sumitomo Chemical Co Ltd
Original Assignee
Agency of Industrial Science and Technology
Sumitomo Chemical 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 Agency of Industrial Science and Technology, Sumitomo Chemical Co Ltd filed Critical Agency of Industrial Science and Technology
Priority to JP23218784A priority Critical patent/JPS61109701A/en
Publication of JPS61109701A publication Critical patent/JPS61109701A/en
Publication of JPH0510323B2 publication Critical patent/JPH0510323B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:A quick-acting herbicide, capable of exhibiting superior herbicidal effect on various weeds such as barnyard grass, oats, an indian mallow and Japanese radish, and containing 2-methyl-2(5)-trifluoromethyl-5-(4)-nitroimidazole as an active ingredient. CONSTITUTION:A herbicide, containing 2-methyl-4(5)-trifluoromethyl- 5(4)- nitroimidazole as an active ingredient, and usually used after formulated into such as an emulsion, wettable powder, suspension and granules mixed with a support, adjuvant, etc. The amount of the active ingredient to be contained in the formulation is within 1-90% range by wt. ratio. The herbicide may also be used in a form mixed with another herbicide, insecticide, fertilizer, soil conditioner, etc. Said herbicide is effective on gramineous weeds such as barnyard grass and oats, broadleaf weeds such as Indian mallow, Japanese radish and Pharbitis purpurea Voigt, commelinaceous weeds, cyperaceous weeds, etc. and used by soil treatment, foliar treatment or treatment under flooding condition as pre-or post-emergence treatment. It is used in paddy field, upland field, orchard, pasture, turf, forest, etc.

Description

【発明の詳細な説明】 る除草剤(以下、本発明組成物と記す。)に関するもの
である。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a herbicide (hereinafter referred to as the composition of the present invention).

本発明組成物は畑地の茎葉処理および土壌処理において
、8題となる種々の雑草、例えばソバカズラ、サナエタ
デヘスペリヒュ、ハコベ、シロザ、アオビユ(アオゲイ
トウ)、ダイコン、ノハラガラシ、ナズナ、アメリカツ
ノクサネム、エビスグサ、イチビ、アメリカキンゴジカ
、フィールドパンジー、ヤエムグラ、アメリカアサガオ
、マルバアサガオ、セイヨウヒルガオ、ヒメオドリコソ
ウ、ホトケノザ、ヨウシュチぎウセンアサガオ、イヌホ
オズキ、オオイヌノフグリ、オナモミ、ヒマワリ、イヌ
カミツレ、コーンマリーゴールド等の広I%雑草、ヒエ
、イヌビエ、エノコログサ、メヒシバ、スズメノカタビ
ラ、ノスズメノテッポウ、エンバク、カラスムギ、セイ
バン毫ロコシ、シバムギ、ウマノチャヒキ、ギ、ウギシ
バ等のイネ科雑草およびツユクサ等のツユクサ科雑草、
コゴメガヤツリ、ハマスゲ等のカヤツリグサ科雑草等に
対して除草動力を有する。しかも、その特徴とするとこ
ろは速効的である。
The composition of the present invention can be used to treat foliage and soil in upland areas, including 8 different types of weeds, such as buckwheat, snailweed, chickweed, whiteweed, blueberry, daikon radish, shepherd's purse, shepherd's purse, American hornwort, Wide range of weeds such as Ebisu grass, Japanese golden deer, Field pansy, Yaemugura, American morning glory, Malva morning glory, Western bindweed, Japanese lily, Hotokenoza, Japanese morning glory, Japanese Physalis, Japanese dogfish, Japanese fir tree, Japanese fir, sunflower, Japanese chamomile, corn marigold, etc. , Poaceae weeds such as barnyard grass, barnyard grass, foxtail grass, black grass, grasshopper, oat, oat, oat, grasshopper, grasshopper, horseweed, cypress, horseweed, and dayflower weeds such as dayflower,
It has weeding power against weeds of the Cyperaceae family, such as Cyperaceae and Cyperaceae. Moreover, its feature is that it is fast-acting.

一ルii J、 Org、 Chem、、 47286
7(1982)  に記載されている化合物である。
Il II J, Org, Chem,, 47286
7 (1982).

本発明組成物を除草剤として用いる場合は、通常固体担
体、液体担体、界面活性剤その他の製剤用補助剤と混合
して、乳剤、永和刑、F3?1iil剤、粒剤等に製剤
する。
When the composition of the present invention is used as a herbicide, it is usually mixed with a solid carrier, a liquid carrier, a surfactant, and other formulation auxiliaries, and formulated into an emulsion, an F3-1IIL agent, a granule, or the like.

ゾールを、!惹比で1〜90g6.好ましくは5〜70
%含有する。
Zor! Attraction ratio: 1-90g6. Preferably 5-70
%contains.

固体担体としては、カオリンクレー、アブタパルジャイ
トクレー、ベントナイト、酸性8土、パイロフィライト
、タルク、珪藻土、方解石、クルミ粉、尿素、硫酸アン
モニウム、合成含水酸化逢累等の微粉末あるいは粒状物
があげられ、液体担体としては、キシレン、メチルナフ
タレン等の芳香族炭化水素類、イソプロパツール、エチ
レングリコール、セロソルブ等のアルコール類、アセト
ン、シクロヘキサノン、イソホロン等のケトン類、大豆
油、綿実油等の植物油、ジメチルスルホキシド、ジメチ
ルホルムアミド、アセトニトリル、水等があげられる。
As solid carriers, fine powders or granules such as kaolin clay, abtapulgite clay, bentonite, acidic 8 earth, pyrophyllite, talc, diatomaceous earth, calcite, walnut powder, urea, ammonium sulfate, and synthetic hydrous oxidation products can be used. Examples of liquid carriers include aromatic hydrocarbons such as xylene and methylnaphthalene, alcohols such as isopropanol, ethylene glycol, and cellosolve, ketones such as acetone, cyclohexanone, and isophorone, and vegetable oils such as soybean oil and cottonseed oil. , dimethyl sulfoxide, dimethyl formamide, acetonitrile, water and the like.

□:     乳化、分散、湿層等のために用いられる
界面活性剤としては、アルキル硫酸エステル塩、アルキ
ルアリールスルホン酸塩、ジアルキルスルホコハク酸塩
、ポリオキシエチレンアルキルアリールエーテルリン酸
エステル塩等の一イオン界面活性剤、ポリオキシエチレ
ンアルキルエーテル、ポリオキシエチレンアルキルアリ
ールエーテル、ポリオキシエチレンポリオキシプロピレ
ンブロックコポリマー、ソルビタン脂肪酸エステル、ポ
リオキシエチレンソルビタン脂肪酸エステル等の非イオ
ン界面活性剤等があげられる。製剤用補助剤としては、
リグニンスルホン酸塩、アルギン酸塩、ポリビニルアル
コール、アラビアガム、CMC(カルボキシメチルセル
ロース)、PAP(fit性リンすイソプロピル)等が
あげられる。
□: Surfactants used for emulsification, dispersion, wet layer, etc. include single ions such as alkyl sulfate salts, alkylaryl sulfonate salts, dialkyl sulfosuccinate salts, and polyoxyethylene alkylaryl ether phosphate salts. Examples include surfactants, nonionic surfactants such as polyoxyethylene alkyl ether, polyoxyethylene alkylaryl ether, polyoxyethylene polyoxypropylene block copolymer, sorbitan fatty acid ester, and polyoxyethylene sorbitan fatty acid ester. As a formulation adjuvant,
Examples include lignin sulfonate, alginate, polyvinyl alcohol, gum arabic, CMC (carboxymethylcellulose), and PAP (isopropyl phosphate).

次に製剤例を示す。部はM置部を示す。Examples of formulations are shown below. The section indicates the M section.

−二トロイミタソール50部、リグニンスルホン酸カル
シウム8部、ラウリル硫酸ナトリウム2部および合成含
水酸化珪素45部をよ(粉砕混合して水和剤を得る。
- 50 parts of ditroimitasol, 8 parts of calcium lignosulfonate, 2 parts of sodium lauryl sulfate, and 45 parts of synthetic hydrated silicon oxide are ground and mixed to obtain a wettable powder.

一二トロイξダゾール10部、ポリオキシエチレンスチ
リルフェニルエーテル14部、ドデシルベンゼンスルホ
ン酸カルシウム6部、キシレン40部およびジメチルホ
ルムアミド80部をよく混合して乳剤を得る。
10 parts of 12-troy ξdazole, 14 parts of polyoxyethylene styryl phenyl ether, 6 parts of calcium dodecylbenzenesulfonate, 40 parts of xylene and 80 parts of dimethylformamide are thoroughly mixed to obtain an emulsion.

−二トロイミグゾール2部、合成含水酸化素1 部、’
Jゲニンスルホン酸カルシウム2部、ベントナイト30
sおよびカオリンクレー65部をよく粉砕混合し、水を
加えてよく練り合せた後、造粒乾燥して粒剤を得る。
- 2 parts of ditroimigsol, 1 part of synthetic hydrous oxide,'
2 parts of calcium J geninsulfonate, 30 parts of bentonite
s and 65 parts of kaolin clay are thoroughly ground and mixed, water is added and the mixture is thoroughly kneaded, followed by granulation and drying to obtain granules.

−二トロイミダゾール25ftB、ポリオキシエチレン
ソルビタンモノオレエート3 部、CMC3部、水69
部を混合し、粒度が5ミクロン以下になる。まで湿式粉
砕して懸濁剤を得る。
-25 ftB of ditroimidazole, 3 parts of polyoxyethylene sorbitan monooleate, 3 parts of CMC, 69 parts of water
The particles are mixed to a particle size of 5 microns or less. Wet grind to obtain a suspension.

ロイシダゾール10部、ポリオキシエチレンスチリルフ
ェニルエーテル1部、水89部を混合し、液剤を得る。
10 parts of leucidazole, 1 part of polyoxyethylene styrylphenyl ether, and 89 parts of water are mixed to obtain a liquid preparation.

このようにして製剤された本発明組成物は、雑草の出芽
前または出芽後に土壌処理、茎葉処理または湛水処理す
る。土壌処理には、土壌表面処理、土壌混和処理等があ
り、茎葉処理には、植物体の上方からの処理のほか、作
物に付着しないよう雑草に@りて処理する局部処理等が
ある。
The composition of the present invention thus formulated is subjected to soil treatment, foliage treatment, or flooding treatment before or after the emergence of weeds. Soil treatment includes soil surface treatment, soil mixing treatment, etc., and foliar treatment includes treatment from above the plant body as well as local treatment of weeds to prevent them from adhering to crops.

また、他の除草剤と混合して用いることにより、除草効
力の増強を期待できる。さらに、殺虫剤、殺ダニ剤、殺
線虫剤、殺菌剤、植物生長調節剤、肥料、土壌改良剤等
と混合して用いることもできる。
Furthermore, by mixing it with other herbicides, it can be expected to increase the herbicidal efficacy. Furthermore, it can be used in combination with insecticides, acaricides, nematicides, fungicides, plant growth regulators, fertilizers, soil conditioners, and the like.

なお、本発明組成物は、水田、畑地、果樹園、牧草地、
芝生地、森林あるいは非農耕地等の除草剤として用いる
ことができる。
The composition of the present invention can be applied to rice fields, fields, orchards, pastures,
It can be used as a herbicide on lawns, forests, non-agricultural lands, etc.

ニトロイミダゾールを本発明組成物の有効成分として用
いる場合、その処理社は、気象条件、製剤形態、処理時
期、方法、場所、対象雑草、対象作物等によっても異な
るが、通常1アールあたり5f〜400 f、好ましく
は、101〜100fであり、乳剤、水和剤、懸濁剤等
は、通常その所定量を1アールあたり1リツトル〜10
リツトルの(必要ならば、展着剤等の補助剤を添加した
)水で希釈して処理し、粒剤等は、通常なんら希釈する
ことなくそのま\処理する。
When nitroimidazole is used as an active ingredient in the composition of the present invention, the processing company usually uses 5f to 400 ml per are, although it varies depending on weather conditions, formulation form, treatment time, method, location, target weeds, target crops, etc. f, preferably from 101 to 100 f, and for emulsions, wetting agents, suspending agents, etc., the predetermined amount is usually 1 liter to 10 f per are.
They are treated by diluting them with a little water (if necessary, with the addition of adjuvants such as spreading agents), while granules and the like are usually treated as they are without any dilution.

展着剤としては、前記の界面活性剤のほか、ポリオキシ
エチレン樹脂酸(エステル)、リグニンスルホン酸塩、
アビエチン酸塩、ジナフチルメタンジスルホン酸塩、パ
ラフィン等があげられる。
In addition to the above-mentioned surfactants, the spreading agents include polyoxyethylene resin acid (ester), lignin sulfonate,
Examples include abietate, dinaphthylmethane disulfonate, and paraffin.

次に、本発明組成物が除草剤として有用であることを試
験例で示す。なお、比較対照に用いた化合物は第1表の
化合物記号で示す。
Next, test examples demonstrate that the composition of the present invention is useful as a herbicide. The compounds used for comparison are indicated by compound symbols in Table 1.

第  1  表 また、除草効力は、調査時の供試植物の出芽および生茸
阻害の程度を肉眼観察し、化合物を供試していない場合
と全くないしほとんど違いがないものを「0」とし、供
試植物が枯死ないし生育が完全に阻害されているものを
「5」として、θ〜5の6段階に評価し、0.1.2.
8.4.5で示す。
Table 1 In addition, herbicidal efficacy was determined by visually observing the degree of inhibition of budding and living mushrooms of test plants during the survey, and ``0'' indicates that there was no or almost no difference from when no compound was tested. If the test plant died or its growth was completely inhibited, it was evaluated as "5", and evaluated on a scale of θ to 5, 0.1.2.
8.4.5.

試験例1 畑地土壌混和処理試験 直径10画、深さ103の円筒プラスチックポットに畑
地土壌を納め、ヒエ、エンバク、ぐ・− オロメチルー5−−トロイミダゾールを乳剤にし、その
所定量を、1アールあたり1oリツトル相当の水で希釈
し、小型噴霧器で土壌表面処理した後、深さ4のまでの
土壌表層部分をよく混和した。処理後20日間温室内で
育成し、除草効力を調査した。その結果を第2表に示す
Test Example 1 Upland Soil Mixing Treatment Test Upland soil was placed in a cylindrical plastic pot with a diameter of 10 squares and a depth of 103 mm, and millet, oat, and g. After diluting with 1 liter of water and treating the soil surface with a small sprayer, the surface layer of the soil up to a depth of 4 was thoroughly mixed. After treatment, the plants were grown in a greenhouse for 20 days and their herbicidal efficacy was investigated. The results are shown in Table 2.

第  2  表 試験例2 畑地茎葉処理試験 直径10cM、深さ10crItの円筒型プラスチック
ポット畑地土壌を詰め、ヒエ、エンバク、゛ダイコン、
イチビを蒲棚し、温室内で1o日ロイミダゾールを水和
剤にし、その所定量を、1アールあたり10リツトル相
当の展着剤を含む水で希釈し、小型噴霧器で植物体の上
方から茎葉処理した。処理後20日間温室内で育成し、
除草力力を調査した。その結果を第3221こホす。
Table 2 Test Example 2 Upland Stem and Leaves Treatment Test Cylindrical plastic pots with a diameter of 10 cm and a depth of 10 cr It were filled with upland soil, and millet, oat, radish,
Straw the Japanese Ichibi into a trellis, use leumidazole as a hydrating agent in a greenhouse for 1 day, dilute the specified amount with water containing a spreading agent equivalent to 10 liters per are, and use a small sprayer to spray the stems and leaves from above the plant. Processed. Grow in a greenhouse for 20 days after treatment,
We investigated the weeding power. The result is 3221st page.

第  8  表 試験例8 畑地茎葉処理試験 面[33X285IN、深さ11cmのバットに畑地土
壌を詰め、ダイズ、ワタ、テンサイ、アサガオ、オナモ
ミ、イチビ、エビスグサ、トウモロコシ、コムギ、イヌ
ビエ、セイバンモロコシ、エノコログサを播種し、18
日f[育成した。その後、製剤例1に準じて2−メ(j
)                  (4)チル−
4−トリフルオロメチル−計コニトロ\l− イミダゾールを水和剤にし、その所定量を、展着剤を含
む1アールあたり5リツトル相当の水で希釈し、小型噴
霧器で植物体の1方から茎葉部全面に均一に処理した。
Table 8 Test Example 8 Field soil, stem, and leaf treatment test surface [33 x 285 IN, 11 cm deep vat was filled with field soil, and soybean, cotton, sugar beet, morning glory, Japanese fir, Japanese grass, corn, wheat, Japanese millet, Seiban sorghum, and hackberry were grown. Sow, 18
Day f [raised. Then, according to Formulation Example 1, 2-Me (j
) (4) Chill-
Make 4-trifluoromethyl-imidazole into a hydrating agent, dilute the specified amount with water equivalent to 5 liters per 1 area including a spreading agent, and spray the stems and leaves from one side of the plant with a small sprayer. The entire surface was treated uniformly.

このとき雑草および作物の生育吠況は華種により異なる
が、1〜4葉期で、草丈は2〜12IMであった。処理
20日後に除草効力を調査した。その結果を第4表に示
す。なお、本試験は、全期間を通して屋外で行った。
At this time, the growth conditions of weeds and crops varied depending on the flower species, but they were in the 1-4 leaf stage and the plant height was 2-12 IM. The herbicidal efficacy was investigated 20 days after the treatment. The results are shown in Table 4. Note that this test was conducted outdoors throughout the entire period.

第  4  表Table 4

Claims (1)

【特許請求の範囲】[Claims] 2−メチル−4(5)−トリフルオロメチル−5(4)
−ニトロイミダゾールを有効成分とすることを特徴とす
る除草剤。
2-Methyl-4(5)-trifluoromethyl-5(4)
- A herbicide characterized by containing nitroimidazole as an active ingredient.
JP23218784A 1984-11-02 1984-11-02 Imidazole based herbicide Granted JPS61109701A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23218784A JPS61109701A (en) 1984-11-02 1984-11-02 Imidazole based herbicide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23218784A JPS61109701A (en) 1984-11-02 1984-11-02 Imidazole based herbicide

Publications (2)

Publication Number Publication Date
JPS61109701A true JPS61109701A (en) 1986-05-28
JPH0510323B2 JPH0510323B2 (en) 1993-02-09

Family

ID=16935360

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23218784A Granted JPS61109701A (en) 1984-11-02 1984-11-02 Imidazole based herbicide

Country Status (1)

Country Link
JP (1) JPS61109701A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014006617A1 (en) * 2012-07-04 2014-01-09 Ramot At Tel-Aviv University Ltd. Ornidazole and related compounds for use as herbicides

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014006617A1 (en) * 2012-07-04 2014-01-09 Ramot At Tel-Aviv University Ltd. Ornidazole and related compounds for use as herbicides
CN104640451A (en) * 2012-07-04 2015-05-20 雷蒙特亚特特拉维夫大学有限公司 Ornidazole and related compounds for use as herbicides
US9237750B2 (en) 2012-07-04 2016-01-19 Ramot At Tel-Aviv University Ltd. Ornidazole and related compounds for use as herbicides

Also Published As

Publication number Publication date
JPH0510323B2 (en) 1993-02-09

Similar Documents

Publication Publication Date Title
JP2536075B2 (en) Herbicidal composition
JPH0768087B2 (en) Herbicide composition
JPH02101004A (en) Herbicidal composition
JPS61109701A (en) Imidazole based herbicide
JP2536587B2 (en) Herbicidal composition
JPH0340001B2 (en)
JP2531235B2 (en) Herbicidal composition
JPH0330562B2 (en)
JPH03127704A (en) Herbicidal composition
JPH0421610A (en) Herbicide composition
JPH0232005A (en) Herbicide composition
JPH0330563B2 (en)
JPH0545594B2 (en)
JP2012097040A (en) Plant disease control composition, and control method of plant disease
JPS61225102A (en) Herbicidal composition
JPS61225103A (en) Herbicidal composition
JPS63179805A (en) Herbicidal composition
JPS63190803A (en) Herbicidal composition
JPS61280402A (en) Herbicidal composition
JPS61280401A (en) Herbicidal composition
JPS59108701A (en) Herbicidal composition
JPS6253906A (en) Herbicidal composition
JPS5989605A (en) Herbicidal composition
JPS63211201A (en) Herbicide composition
JPS6141490B2 (en)

Legal Events

Date Code Title Description
EXPY Cancellation because of completion of term