JP2943003B2 - Field-acting herbicide composition and herbicidal method - Google Patents

Field-acting herbicide composition and herbicidal method

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Publication number
JP2943003B2
JP2943003B2 JP17098990A JP17098990A JP2943003B2 JP 2943003 B2 JP2943003 B2 JP 2943003B2 JP 17098990 A JP17098990 A JP 17098990A JP 17098990 A JP17098990 A JP 17098990A JP 2943003 B2 JP2943003 B2 JP 2943003B2
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JP
Japan
Prior art keywords
herbicide
compound
parts
weeds
field
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.)
Expired - Fee Related
Application number
JP17098990A
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Japanese (ja)
Other versions
JPH0459706A (en
Inventor
勉 馬渕
功 柳井
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.)
NIPPON NOYAKU KK
Original Assignee
NIPPON NOYAKU KK
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Priority to JP17098990A priority Critical patent/JP2943003B2/en
Publication of JPH0459706A publication Critical patent/JPH0459706A/en
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Publication of JP2943003B2 publication Critical patent/JP2943003B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は一般式(I) (式中、Rは低級アルキル基を示し、Xはハロゲン原子
を示す。) で表される3−置換フェニルピラゾール誘導体とフェニ
ルウレア系除草剤又はフェノキシ脂肪酸系除草剤から選
択される1種又は2種以上の化合物とを有効成分として
含有することを特徴とする畑作用除草剤組成物及び防除
方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a compound represented by the general formula (I) (Wherein, R represents a lower alkyl group, and X represents a halogen atom). One or two selected from a 3-substituted phenylpyrazole derivative represented by the following formula and a phenylurea herbicide or a phenoxy fatty acid herbicide. Field of the Invention The present invention relates to a field-acting herbicide composition and a method for controlling herbicides, which comprise at least one compound as an active ingredient.

現在、畑作の小麦、大麦、大豆、トウモロコシ等の作
物の栽培において、雑草を防除する目的で種々の除草剤
が使用されているが、畑作においては防除の対象となる
雑草の種類は多く、その発生も長期間にわたるため、使
用される除草剤も幅広い殺草スペクトラムを有するもの
で、作物に対して安全で且つ低薬量で高い除草効果を示
す除草剤が求められている。
Currently, in the cultivation of crops such as wheat, barley, soybeans, corn and the like in upland cultivation, various herbicides are used for the purpose of controlling weeds.In upland cultivation, there are many types of weeds to be controlled. Since the outbreak occurs over a long period of time, herbicides to be used also have a broad herbicidal spectrum, and there is a need for a herbicide that is safe for crops and that exhibits a high herbicidal effect at a low dose.

本発明者等は上記現状を鑑み、殺草スペクトラムが広
く、長期間にわたって雑草の発生を防止し、作物に対し
て安全で且つ低薬量で除草効果を示す除草剤を創出すべ
く鋭意研究を重ねた結果、上記一般式(I)で表される
3−置換フェニルピラゾール誘導体とフェニルウレア系
除草剤又はフェノキシ脂肪酸系除草剤から選択される1
種又は2種以上の化合物とを組み合わせることにより、
各々の化合物を単独で使用した場合に比して、予測し得
ない程の相乗効果を示し、これにより薬量の低減化が図
られ、且つ草殺スペクトラムが拡大することを見出し、
本発明を完成させたものである。
In view of the above situation, the present inventors have conducted intensive studies to create a herbicide that has a wide herbicidal spectrum, prevents the occurrence of weeds for a long period of time, and is safe and has a low herbicidal effect on crops. As a result of the superposition, 1 selected from the 3-substituted phenylpyrazole derivative represented by the above general formula (I) and a phenylurea herbicide or a phenoxy fatty acid herbicide.
By combining a species or two or more compounds,
Compared to the case where each compound is used alone, it shows an unexpectedly synergistic effect, thereby reducing the dose and finding that the herbicidal spectrum is expanded,
The present invention has been completed.

本発明の一方の有効成分である一般式(I)で表され
る3−置換フェニルピラゾール誘導体は本出願人が特願
昭63−217164号及び特願平1−225724号において除草剤
として出願を行った化合物であり、その代表的な化合物
を第1表に例示する。
One of the active ingredients of the present invention, a 3-substituted phenylpyrazole derivative represented by the general formula (I), was filed by the present applicant as a herbicide in Japanese Patent Application Nos. 63-217164 and 1-2225724. Table 1 shows typical compounds.

一般式(I) 本発明で使用できる他方の有効成分の一種であるフェ
ニルウレア系除草剤としては、例えば、 f.3−(4−イソプロピルフェニル)−1,1−ジメチルウ
レア(一般名イソプロツロン、The PESTICIDE INDEX,7t
h.edition,P329) g.3−(3,4−ジクロロフェニル)−1,1−ジメチルウレ
ア(一般名ジウロン、同P226) h.3−(3,4−ジクロロフェニル)−1−メトキシ−1−
ジメチルウレア(一般名リニュロン、同P336) i.3−(4−クロロフェニル)−1,1−ジメチルウレア
(一般名モニュロン、同P386).フェノキシ脂肪酸系除
草剤としては、4−クロロ−2−メチルフェノキシ酢
酸、その塩又はエステル、例えば、 j.4−クロロ−o−トリルオキシ酢酸、そのナトリウム
又はカリウム塩(一般名MCP) k.4−クロロ−o−トリルオキシ酢酸エチル(一般名MCP
−エチル) l.4−クロロ−o−トリルオキシ酢酸ブチル(一般名MCP
−ブチル) 4−クロロ−2−メチルフェノキシプロピオン酸、そ
の塩又はエステル、例えば、 m.4−クロロ−o−トリルオキシプロピオン酸、そのカ
リウム塩又はジエタノールアミン塩(一般名MCPP) n.4−クロロ−o−トリルオキシ酢酸又はそのナトリウ
ム塩(一般名MCPB) 等のフェニルウレア系化合物又はフェノキシ脂肪酸系化
合物を例示することができるが、本発明は上記化合物に
限定されるものではなく、本発明の一方の有効成分であ
る3−置換フェニルピラゾール誘導体と混合して使用す
ることにより、同様の効果を奏するものであれば良い。
General formula (I) Examples of the phenylurea herbicide which is one of the other active ingredients that can be used in the present invention include f.3- (4-isopropylphenyl) -1,1-dimethylurea (generic name: isoproturon, The PESTICIDE INDEX, 7t).
h.edition, P329) g.3- (3,4-dichlorophenyl) -1,1-dimethylurea (generic names diuron, P226) h.3- (3,4-dichlorophenyl) -1-methoxy-1-
Dimethylurea (generic name Linuron, P336) i.3- (4-Chlorophenyl) -1,1-dimethylurea (generic name Monuron, P386). Examples of phenoxy fatty acid herbicides include 4-chloro-2-methylphenoxyacetic acid, salts or esters thereof, for example, j.4-chloro-o-tolyloxyacetic acid, sodium or potassium salt thereof (generic name: MCP) k.4- Ethyl chloro-o-tolyloxyacetate (generic name: MCP
-Ethyl) l.4-Butyl-o-tolylbutyl oxyacetate (generic name MCP
-Butyl) 4-chloro-2-methylphenoxypropionic acid, a salt or ester thereof, for example, m.4-chloro-o-tolyloxypropionic acid, a potassium salt or a diethanolamine salt (common name MCPP) n.4-chloro Examples thereof include phenylurea-based compounds and phenoxy fatty acid-based compounds such as -o-tolyloxyacetic acid or its sodium salt (generic name: MCPB), but the present invention is not limited to the above compounds, and one of the present invention The same effect can be obtained by mixing and using the 3-substituted phenylpyrazole derivative which is the active ingredient of the above.

本発明の除草剤組成物は、畑作における種々の雑草、
特に小麦、大麦等の穀物畑における広範囲の種類の雑草
に対して低薬量で優れた除草効果を示し、且つ作物に対
してと薬害を示さない選択性の優れた除草剤組成物であ
る。
The herbicidal composition of the present invention comprises various weeds in upland crops,
In particular, the present invention is a herbicide composition exhibiting an excellent herbicidal effect at a low dose and a wide range of weeds in a cereal field such as wheat and barley at a low dose and exhibiting no harm to crops.

本発明の除草剤組成物は、畑作における種々の雑草、
特に小麦、大麦等の穀物畑における雑草、例えばヤエム
グラ、ハコベ、オオイヌノフグリ、スミレ、イヌカミツ
レ、グンバイナズナ、オロシャギク、ノハラガラシ、ヒ
メオドリコソウ、エゾキツネアザミ、ワスレナグサ、ハ
ルタデ、サナエタデ、オランダミミナグサ、ソバカズ
ラ、セイヨウヒルガオ、シロザ、アオゲイトウ、イヌホ
ウズキ等の双子葉植物に対して優れた除草効果を示す
他、イネ科雑草であるセイヨウヌカボ、スズメノテッポ
ウ等に対しても除草効果を示すものである。
The herbicidal composition of the present invention comprises various weeds in upland crops,
In particular, weeds in cereal fields such as wheat and barley, such as yamgra, chickweed, giant petrel, violets, dog chamomile, gumbinazuna, oroshaku, haragarashi, himeodorikosou, suzukusyuthisami, forget-me-nots, haradade, sasa-e-o-a, sasa-e-o-a-na-g-a, sasa-e-o-a-na-g, In addition to its excellent herbicidal effect on dicotyledonous plants such as dogwood, etc., it also has a herbicidal effect on grass weeds such as P. brassicae and P. perennial.

本発明の除草剤組成物は、特に従来防除が困難な雑
草、例えばヤエムグラ、ハコベ、オオイヌノフグリ、ス
ミレ、イヌカミツレ、グンバイナズナ、ハルタデ、サナ
エタデ、ソバカズラ等を同時に防除することができる。
The herbicidal composition of the present invention can simultaneously control, in particular, weeds that have been difficult to control in the past, such as yamgra, chickweed, giant petrel, violet, dog chamomile, gumbinazuna, halade, sanaetade, buckwheat.

本発明の除草剤組成物を使用する場合、農薬製剤上の
常法に従い、目的に応じて適当な剤型に製造して使用す
れば良く、例えば固体担体、液体担体、界面活性剤、そ
の他必要に応じて補助剤等と混合して粒剤、水和剤、粉
剤、フロアブル剤、液剤等の剤型に調製して使用すれば
良い。
When the herbicidal composition of the present invention is used, it may be manufactured and used in an appropriate dosage form according to the purpose according to a conventional method for pesticide formulation. For example, a solid carrier, a liquid carrier, a surfactant, and other necessary components may be used. May be mixed with adjuvants and the like to prepare granules, wettable powders, powders, flowables, liquids and the like and use them.

本発明の除草剤組成物の有効成分は剤型に応じて任意
の割合で配合することができ、又組成物中の有効成分の
配合割合は、一般式(I)で表される3−置換フェニル
ピラゾール誘導体及びフェニルウレア系除草剤化合物又
はフェノキシ脂肪酸系除草剤化合物を任意の割合で混合
すれば良く、通常は一般式(I)で表される3−置換フ
ェニルピラゾール誘導体1重量部に対してフェニルウレ
ア系化合物では1〜5000重量部の範囲から選択すれば良
く、好ましくは5〜1000重量部であり、フェノキシ脂肪
酸系化合物では1〜1000重量部の範囲から選択すれば良
く、好ましくは1〜500重量部の範囲である。
The active ingredient of the herbicidal composition of the present invention can be blended in an arbitrary ratio according to the dosage form, and the blending ratio of the active ingredient in the composition is based on the 3-substituted compound represented by the general formula (I). The phenylpyrazole derivative and the phenylurea-based herbicide compound or the phenoxy fatty acid-based herbicide compound may be mixed at an arbitrary ratio, and is usually used with respect to 1 part by weight of the 3-substituted phenylpyrazole derivative represented by the general formula (I). The phenylurea compound may be selected from the range of 1 to 5000 parts by weight, preferably 5 to 1000 parts by weight, and the phenoxy fatty acid compound may be selected from the range of 1 to 1000 parts by weight, preferably 1 to 1000 parts by weight. It is in the range of 500 parts by weight.

本発明の除草剤組成物は、例えば小麦畑地に使用する
場合、小麦及び雑草の発生初期から生育期にかけて使用
することができる。
When the herbicidal composition of the present invention is used, for example, in a wheat field, it can be used from the early stage of the development of wheat and weeds to the growing season.

又本発明はこれらの時期に限らず、小麦及び雑草の発
生前に土壌処理することもできるが、好ましくは発生初
期乃至生育期に処理するのが良い。
In addition, the present invention is not limited to these periods, and it is also possible to treat the soil before the emergence of wheat and weeds.

本発明の除草剤組成物の処理量は、本発明の除草剤組
成物の有効性分量として1ヘクタール当たり0.1〜6000g
の範囲から選択して使用すれば良い。
The treatment amount of the herbicidal composition of the present invention is 0.1 to 6000 g per hectare as the effective amount of the herbicidal composition of the present invention.
It can be used by selecting from the range.

以下に本発明の代表的な実施例を示すが、本発明はこ
れらに限定されるものではない。
Hereinafter, typical examples of the present invention will be described, but the present invention is not limited thereto.

尚、実施例中、部とあるのは重量部を示す。 In Examples, “parts” means “parts by weight”.

実施例1. 化合物1 0.5部 化合物f 2.0部 含水珪酸微粉末 1.0部 ポリビニルアルコール 0.5部 珪砂 96.0部 以上を均一に混合粉砕して、適量の水を加えて混練
し、造粒・乾燥して粒剤とする。
Example 1. Compound 1 0.5 part Compound f 2.0 part Hydrous silicic acid fine powder 1.0 part Polyvinyl alcohol 0.5 part Silica sand 96.0 parts The above components are uniformly mixed and pulverized, kneaded with an appropriate amount of water, granulated and dried to obtain granules. Agent.

実施例2. 化合物4 1.0部 化合物j 8.0部 含水珪酸微粉末 2.0部 ポリビニルアルコール 0.5部 珪砂 88.5部 以上を均一に混合粉砕して、適量の水を加えて混練
し、造粒・乾燥して粒剤とする。
Example 2. Compound 4 1.0 part Compound j 8.0 parts Hydrous silicic acid fine powder 2.0 parts Polyvinyl alcohol 0.5 parts Silica sand 88.5 parts The above components are uniformly mixed and pulverized, kneaded by adding an appropriate amount of water, granulated and dried to obtain granules. Agent.

実施例3. 化合物4 20.0部 化合物f 40.0部 ラウリル硫酸ナトリウム 3.0部 リグニンスルホン酸カルシウム 3.0部 含水珪酸微粉末 7.0部 クレー粉末 27.0部 以上を均一に混合粉砕して、水和剤とする。Example 3 Compound 4 20.0 parts Compound f 40.0 parts Sodium lauryl sulfate 3.0 parts Lignin sulfonate calcium 3.0 parts Hydrous silicate fine powder 7.0 parts Clay powder 27.0 parts The above are uniformly mixed and pulverized to obtain a wettable powder.

実施例4. 化合物4 10.0部 化合物j 20.0部 ラウリル硫酸ナトリウム 3.0部 リグニンスルホン酸カルシウム 3.0部 含水珪酸微粉末 5.0部 クレー粉末 59.0部 以上を均一に混合粉砕して、水和剤とする。Example 4. Compound 4 10.0 parts Compound j 20.0 parts Sodium lauryl sulfate 3.0 parts Lignin calcium sulfonate 3.0 parts Hydrous silicate fine powder 5.0 parts Clay powder 59.0 parts The above are uniformly mixed and pulverized to obtain a wettable powder.

実施例5. 化合物1 5.0部 化合物f 15.0部 ポリオキシエチレンノニルフェニルエーテル 1.5部 ポリオキシエチレンスチレン化フェニルエーテル 1.5部 キサンタンガム 0.2部 エチレングリコール 5.0部 水 71.8部 以上を均一に混合し、湿式粉砕してフロアブル剤とす
る。
Example 5. Compound 1 5.0 parts Compound f 15.0 parts Polyoxyethylene nonyl phenyl ether 1.5 parts Polyoxyethylene styrenated phenyl ether 1.5 parts Xanthan gum 0.2 parts Ethylene glycol 5.0 parts Water 71.8 parts The above are uniformly mixed and wet-pulverized. A flowable agent.

試験例1.本発明組成物の相乗効果 直径12cm、高さ11cmのポットに畑地土壌を充填し、オ
オイノフグリの種子を覆土深0.5cmで播種し、温室内で
生育させた。
Test Example 1. Synergistic Effect of the Composition of the Present Invention A pot having a diameter of 12 cm and a height of 11 cm was filled with field soil, and seeds of Ooinofugu were sown at a covering soil depth of 0.5 cm and grown in a greenhouse.

オオイノフグリが3葉期、草丈8cmとなった時、本発
明の除草剤組成物の所定量を水で希釈し、1ヘクタール
当たり500の割合で、植物体の上方から小型噴霧器で
茎葉全面に均一に散布した。散布後21日目に枯れ残った
オオイノフグリの地上部生体重を計り、次式により生体
重抑制率(%)を算出した。
When Ooinoufu-guri reaches the 3 leaf stage and the height of the plant is 8 cm, a predetermined amount of the herbicidal composition of the present invention is diluted with water, and at a rate of 500 per hectare, the entire foliage is uniformly spread from above the plant with a small sprayer. Sprayed. On the 21st day after the spraying, the above-ground living weight of the withering ogre was measured, and the living weight inhibition rate (%) was calculated by the following equation.

それぞれの試験結果を第3表乃至第7表に示す。 Tables 3 to 7 show the test results.

上記の結果をよりわかりやすくするために図で示す。 The above results are shown graphically for better understanding.

第1図は試験例中の第1表のオオイヌノフグリに対す
る除草効果をもとに等効果線法により作図したものであ
る。横軸は化合物1の有効成分量(g/ha)を表し、縦軸
は化合物aの有効成分成分量(g/ha)を表す。地上部生
体重抑制率90%の相加効果を破線で示し、実際の地上部
生体重抑制率90%の等効果線を実線で示した。
FIG. 1 is a diagram plotted by an iso-effect method based on the herbicidal effect on the giant beetle in Table 1 in the test examples. The horizontal axis represents the amount of the active ingredient of compound 1 (g / ha), and the vertical axis represents the amount of the active ingredient of compound a (g / ha). The additive effect of 90% above-ground living weight suppression rate is indicated by a dashed line, and the actual iso-effect line of 90% above-ground living weight suppression rate is indicated by a solid line.

第2図は第1図と同様にして示す。 FIG. 2 is shown in the same manner as FIG.

第1図及び第2図に示すごとく、本発明の除草剤組成
物は明らかに相乗効果を示している。
As shown in FIGS. 1 and 2, the herbicidal composition of the present invention clearly shows a synergistic effect.

【図面の簡単な説明】[Brief description of the drawings]

第1図及び第2図は本発明の除草剤組成物の相乗効果を
等効果線法により示すグラフである。
FIG. 1 and FIG. 2 are graphs showing the synergistic effect of the herbicidal composition of the present invention by the isometric method.

Claims (6)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】一般式(I) (式中、Rは低級アルキル基を示し、Xはハロゲン原子
を示す。) で表される3−置換フェニルピラゾール誘導体とフェニ
ルウレア系除草剤又はフェノキシ脂肪酸系除草剤から選
択される1種又は2種以上の化合物とを有効成分として
含有することを特徴とする畑作用除草剤組成物。
1. The compound of the general formula (I) (Wherein, R represents a lower alkyl group, and X represents a halogen atom). One or two selected from a 3-substituted phenylpyrazole derivative represented by the following formula and a phenylurea herbicide or a phenoxy fatty acid herbicide. A field-acting herbicide composition comprising at least one compound as an active ingredient.
【請求項2】一般式(I)で表される3−置換フェニル
ピラゾール誘導体1重量部に対してフェニルウレア系除
草剤又はフェノキシ脂肪酸系除草剤を1〜5000重量部の
割合で含有することを特徴とする請求項第1項記載の畑
作用除草剤組成物。
2. A phenylurea herbicide or a phenoxy fatty acid herbicide in a proportion of 1 to 5000 parts by weight per 1 part by weight of a 3-substituted phenylpyrazole derivative represented by the general formula (I). The herbicidal composition for field action according to claim 1, characterized in that:
【請求項3】麦用である請求項第2項記載の畑作用除草
剤組成物。
3. The herbicidal composition for field action according to claim 2, which is for wheat.
【請求項4】畑作作物の生育に対して望ましからぬ雑草
を防除するために、一般式(I) (式中、Rは低級アルキル基を示し、Xはハロゲン原子
を示す。) で表される3−置換フェニルピラゾール誘導体とフェニ
ルウレア系除草剤又はフェノキシ脂肪酸系除草剤から選
択される1種又は2種以上の化合物とを有効成分として
含有する畑作用除草剤組成物を1ヘクター当たり有効成
分量として0.1〜6000gの範囲で処理することを特徴とす
る畑作における雑草の防除方法。
4. Formula (I) for controlling undesired weeds against the growth of upland crops. (Wherein, R represents a lower alkyl group, and X represents a halogen atom). One or two selected from a 3-substituted phenylpyrazole derivative represented by the following formula and a phenylurea herbicide or a phenoxy fatty acid herbicide. A method for controlling weeds in upland crops, comprising treating a field-acting herbicide composition containing at least one kind of compound as an active ingredient in an amount of 0.1 to 6000 g as an active ingredient per hectare.
【請求項5】畑作作物が麦である請求項第4項記載の雑
草の防除方法。
5. The method for controlling weeds according to claim 4, wherein the upland crop is wheat.
【請求項6】畑作作物及び雑草の発生始期乃至生育期に
処理する請求項第5項記載の雑草の防除方法。
6. The method for controlling weeds according to claim 5, wherein the treatment is carried out from the beginning to the growing stage of upland crops and weeds.
JP17098990A 1990-06-28 1990-06-28 Field-acting herbicide composition and herbicidal method Expired - Fee Related JP2943003B2 (en)

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Application Number Priority Date Filing Date Title
JP17098990A JP2943003B2 (en) 1990-06-28 1990-06-28 Field-acting herbicide composition and herbicidal method

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JP2943003B2 true JP2943003B2 (en) 1999-08-30

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2920446B2 (en) * 1992-10-27 1999-07-19 日本農薬株式会社 Herbicide composition and herbicidal method
AU653299B2 (en) * 1993-02-06 1994-09-22 Nihon Nohyaku Co., Ltd. A herbicidal composition having a reduced phytotoxicity
AU654927B2 (en) * 1993-04-04 1994-11-24 Nihon Nohyaku Co., Ltd. Herbicidal composition for upland farming and weeding method
JP2759407B2 (en) * 1993-04-15 1998-05-28 ローレルバンクマシン株式会社 Coin wrapping machine
FR2705202B1 (en) * 1993-05-19 1996-04-12 Rhone Poulenc Agrochimie Herbicide mixtures based on bromoxynil and a 3-phenylpyrazole compound.
FR2705201B1 (en) * 1993-05-19 1995-07-07 Rhone Poulenc Agrochimie Herbicide mixtures based on diflufenican and a 3-phenylpyrazole compound.
FR2726971B1 (en) * 1994-11-18 1998-12-11 Rhone Poulenc Agrochimie HERBICIDAL MIXTURES BASED ON 3-PHENYLPYRAZOLE DERIVATIVES AND BIFENOX

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