JPH08245311A - Composition for agricultural and horticultural pest control - Google Patents

Composition for agricultural and horticultural pest control

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Publication number
JPH08245311A
JPH08245311A JP7080795A JP7080795A JPH08245311A JP H08245311 A JPH08245311 A JP H08245311A JP 7080795 A JP7080795 A JP 7080795A JP 7080795 A JP7080795 A JP 7080795A JP H08245311 A JPH08245311 A JP H08245311A
Authority
JP
Japan
Prior art keywords
agricultural
methyl
pest control
compound
effect
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
JP7080795A
Other languages
Japanese (ja)
Inventor
Akira Wakai
彰 若井
Hiroyasu Hosokawa
浩靖 細川
Hiroyuki Tanaka
浩行 田中
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 Soda Co Ltd
Original Assignee
Nippon Soda 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 Nippon Soda Co Ltd filed Critical Nippon Soda Co Ltd
Priority to JP7080795A priority Critical patent/JPH08245311A/en
Publication of JPH08245311A publication Critical patent/JPH08245311A/en
Pending legal-status Critical Current

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Abstract

PURPOSE: To obtain an agricultural and horticultural pest control composition expressing a synergistic effect for an antibacterial effect and a pesticidal and acaricidal effect by allowing to contain methylmethoxyiminotolyloxytolyl acetate, etc., and fenpyrade, etc., as effective ingredients. CONSTITUTION: This agricultural and horticultural pest control composition contains (A) one or more compounds selected from the group consisting of N-methyl-(E)-methoxyimino[α-(O-tolyloxy-O-tolyl] acetate, methyl-(E)-2- 2-[6-(2- cyanophenoxy)pyrimidine-4-yloxyl]phenyl-3-methoxy acrylate and (E)-2- methoxyimino-N-methyl-2-(2-phenoxyphenyl) acetamide (B) one or more compounds selected from the group consisting of fenpyrade, fenpyroximate and pyridaben. The mixing ratio of the ingredient A/ingredient B is preferably 4/1-1/4 in weight ratio.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、有害生物に対して優れ
た共力ないし相乗的に殺菌および殺虫殺ダニ作用を示す
農園芸用有害生物防除薬剤に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a pest control agent for agricultural and horticultural use which exhibits excellent synergistic or synergistic bactericidal and insecticidal acaricidal action against pests.

【0002】[0002]

【従来の技術】従来から作物を加害する有害生物を防除
するには数多くの農園芸用防除薬剤が使用されている
が、なお種々の面で改良が望まれている。例えば、メト
キシアクリレート関連殺菌剤は、農園芸上有害なうどん
こ病、黒星病、さび病などの病原菌に対して生育阻害を
示すことが知られているが、灰色かび病や菌核病などの
特定の病害に対してはその効果が十分でない。また、殺
ダニ剤のフェンピラド、フェンピロキシメート、ピリダ
ベンなどは、最近それらの薬剤に対して抵抗性を示すダ
ニの発生により、その有用性を失いつつある。
2. Description of the Related Art Conventionally, many agricultural and horticultural control agents have been used for controlling pests that harm crops, but improvements are still desired in various aspects. For example, methoxyacrylate-related fungicides are known to show growth inhibition against pathogenic bacteria such as powdery mildew, scab, and rust, which are harmful to agriculture and horticulture, but such as gray mold and sclerotia. Its effect is not sufficient for certain diseases. In addition, the miticides fenpyrad, fenpyroximate, pyridaben, etc. are losing their usefulness due to the recent occurrence of mites resistant to these drugs.

【0003】[0003]

【本発明が解決しようとする課題】本発明は、複数種の
薬剤を混合することによって、前記薬剤の欠点を補い、
各薬剤単独では不十分な殺菌、殺虫および殺ダニ活性に
高い効果を示す農園芸用有害生物防除組成物を提供する
ことを目的とする。
SUMMARY OF THE INVENTION The present invention compensates for the drawbacks of the above-mentioned drugs by mixing a plurality of drugs.
It is an object of the present invention to provide a pest control composition for agricultural and horticultural use, which shows high effects on bactericidal, insecticidal and acaricidal activities which are insufficient with each agent alone.

【0004】[0004]

【課題を解決するための手段】本発明は、メトキシアク
リレート関連殺菌剤の少なくとも1種とフェンピラド、
フェンピロキシメート、ピリダベンの少なくとも1種と
を有効成分として含有することを特徴とする農園芸用有
害生物防除組成物である。
The present invention is directed to at least one fungicide related to methoxyacrylate and fempirad,
A pest control composition for agricultural and horticultural use, which comprises, as an active ingredient, at least one of fenpyroximate and pyridaben.

【0005】本発明殺菌組成物の有効成分の一つである
メトキシアクリレート関連殺菌剤とは、例えば、特開平
2−264765号、特開平3−246268号、特開
平3−284659号、特開平4−89464号、特開
平4−182461号、特開平5−43533号、特開
平5−78301号および特開平5−163249号公
報等に記載された殺菌性化合物をいい、イミノ酢酸ある
いはアクリル酸部分を部分構造として分子中に有するこ
とを特徴とする。これら作用性が共通する化合物群はす
べて本発明にいうメトキシアクリレート関連殺菌剤に含
まれる。
The methoxyacrylate-related bactericide which is one of the active ingredients of the bactericidal composition of the present invention is, for example, JP-A-2-264765, JP-A-3-246268, JP-A-3-284659 or JP-A-4. -89464, JP-A-4-182461, JP-A-5-43333, JP-A-5-78301, and JP-A-5-163249. It is characterized by having a partial structure in the molecule. All of these compounds having a common action are included in the methoxyacrylate-related fungicides referred to in the present invention.

【0006】メトキシアクリレート関連殺菌剤として、
具体的には、メチル−(E)−メトキシイミノ[α−
(O−トリロキシ−O−トリル]アセテート(以下「化
合物(A)という)、メチル−(E)−2−{2−[6
−(2−シアノフェキシ)ピリミジン−4−イルオキ
シ]フェニール}−3−メトキシアクリレート(以下
「化合物(B)という)、および(E)−2−メトキシ
イミノ−N−メチル−2−(2−フェノキシフェニー
ル)アセタミド(以下「化合物(C)という)などが挙
げられる。
As a fungicide related to methoxy acrylate,
Specifically, methyl- (E) -methoxyimino [α-
(O-triloxy-O-tolyl] acetate (hereinafter referred to as “compound (A)”), methyl- (E) -2- {2- [6
-(2-Cyanophenoxy) pyrimidin-4-yloxy] phenyl} -3-methoxyacrylate (hereinafter referred to as "compound (B)"), and (E) -2-methoxyimino-N-methyl-2- (2-phenoxyphenyl) ) Acetamide (hereinafter referred to as “compound (C)”) and the like.

【0007】本発明のメトキシアクリレート関連殺菌剤
の化合物(A)、(B)、(C)は単独では灰色かび病
などに対して十分な効果を示さない。また、これらの化
合物は殺ダニおよび殺虫効果を有さない。
The compounds (A), (B), and (C) of the methoxyacrylate-related fungicides of the present invention alone do not show a sufficient effect against Botrytis cinerea. Also, these compounds have no acaricidal or insecticidal effect.

【0008】本発明のもう一方の有効成分は、フェンピ
ラド(以下、「化合物(D)、フェンピロキシメート
(以下、「化合物(E)という)およびピリダベン(以
下、「化合物(F)という)である。これらの殺ダニ剤
の化合物(D)、(E)および(F)は、最近これらの
薬剤に対して抵抗性となったハダニが発生したため、そ
の有用性が失われつつあり、今後の防除に警告がなされ
ている(平成6年度日本昆虫学会第54回大会、第38
回日本応用動物昆虫学会大会合同大会講演要旨248
頁)。また、アブラムシ類に対して殺虫効果があるが、
その効果は十分なものではないことから、さらに一層の
高い効力が望まれている。また、これらは灰色かび病な
どに対してほとんど殺菌活性を有さない化合物である。
The other active ingredient of the present invention is fenpyrad (hereinafter referred to as "compound (D), fenpyroximate (hereinafter referred to as" compound (E) ") and pyridaben (hereinafter referred to as" compound (F) "). The compounds (D), (E) and (F), which are acaricides, are losing their usefulness due to the recent occurrence of spider mites that have become resistant to these agents, and warn future control. (The 54th Annual Conference of the Japanese Society of Entomology, 1994, 38th
248th Annual Meeting of Japan Society for Applied Animal Entomology
page). It also has an insecticidal effect on aphids,
Since the effect is not sufficient, even higher efficacy is desired. Further, these are compounds having little bactericidal activity against Botrytis cinerea.

【0009】本発明者らは、上記メトキシアクリレート
関連殺菌剤の化合物および上記殺ダニ剤を含有してなる
組成物が、単独では認められなかった殺菌、殺虫、殺ダ
ニ活性に優れた相乗効果を発揮することを見いだし、本
発明を完成した。
The inventors of the present invention have found that a composition comprising the above-mentioned methoxyacrylate-related fungicide compound and the above-mentioned acaricide has a synergistic effect which is not observed by itself and has an excellent bactericidal, insecticidal and acaricidal activity. The present invention has been completed by discovering that it can be demonstrated.

【0010】本発明において、上記有効成分を担体とす
る場合、化合物(A)、(B)または(C)のいずれか
一つと化合物(D)(E)または(F)のいずれか一つ
の混合比は任意であるが、その相乗効果がもたらされる
ように、一般的には1:100〜100:1、より好ま
しくは4:1〜1:4になされる。混合物の相乗効果は
組成物の殺菌、殺ダニ効果が、各有効化合物それぞれの
殺菌、殺ダニ効果よりも大きいことにより示される。
In the present invention, when the above-mentioned active ingredient is used as a carrier, a mixture of any one of the compounds (A), (B) or (C) and any one of the compounds (D) (E) or (F). The ratio is arbitrary, but is generally 1: 100 to 100: 1, more preferably 4: 1 to 1: 4 so as to bring about the synergistic effect. The synergistic effect of the mixture is indicated by the fact that the fungicidal and acaricidal effect of the composition is greater than the fungicidal and acaricidal effect of each active compound.

【0011】実際的には、純粋な化合物(A)、(B)
または(C)のいずれか一つと化合物(D)(E)また
は(F)のいずれか一つを使用するが、例えば他の殺菌
剤殺ダニ剤や殺虫剤、殺線虫剤、除草剤、植物生長調節
剤および固着剤、展着剤等の補助剤などを添加すること
もできる。
Practically, pure compounds (A) and (B)
Or any one of (C) and any one of the compounds (D), (E) or (F) are used, and for example, other fungicides, acaricides, nematicides, herbicides, It is also possible to add a plant growth regulator and an auxiliary agent such as a sticking agent and a spreading agent.

【0012】本発明を実施するには、後述の実施例に示
すごとく化合物(A)、(B)または(C)のいずれか
一つと化合物(D)、(E)または(F)のいずれか一
つを含有する通常の農薬の形態即ち水和剤、乳剤、ドラ
イフロアブル、フロアブルを製造するか、あるいは別々
に製造したものをさらに混合して行われる。
In order to carry out the present invention, any one of the compounds (A), (B) or (C) and any one of the compounds (D), (E) or (F) as shown in the examples below. A conventional pesticide form containing one, i.e., a wettable powder, an emulsion, a dry flowable, a flowable, is prepared, or those prepared separately are further mixed.

【0013】[0013]

【実施例】次に実施例を挙げて本発明を具体的に説明す
る。 (実施例1) フロアブル剤 化合物(A) 20.8部 化合物(D) 5部 プロピレングリコール 8部 ポリカルボン酸ソーダ 7部 EO付加トリスチリルフェニールエーテル 4部 シリコン系消泡剤 0.5部 キサンダンガム 0.2部 水 54.5部 以上を湿式で微細に粉砕して有効成分21.3%のフロ
アブルを得た。
EXAMPLES Next, the present invention will be specifically described with reference to examples. (Example 1) Flowable compound 20.8 parts Compound (A) 5 parts Compound (D) 5 parts Propylene glycol 8 parts Sodium polycarboxylic acid 7 parts EO-added tristyrylphenyl ether 4 parts Silicone antifoam 0.5 parts Xanthane gum 0 2 parts Water 54.5 parts The above was finely pulverized by a wet method to obtain a flowable product containing 21.3% of the active ingredient.

【0014】 (実施例2) 水和剤 化合物(A) 23.5部 化合物(D) 5部 クレー 53.5部 アルギンベンゼンスルホン酸ソーダ 3部 ナフタレンスルホン酸ホルムアルデヒド縮合物 5部 リグニンスルホン酸ソーダ 10部 以上を均一に混合、微細に粉砕して有効成分28.5%
の水和剤を得た。
(Example 2) Wettable powder Compound (A) 23.5 parts Compound (D) 5 parts Clay 53.5 parts Sodium alginate benzene sulfonate 3 parts Naphthalene sulfonic acid formaldehyde condensate 5 parts Sodium lignin sulfonate 10 28.5% of active ingredient
A wettable powder of

【0015】[0015]

【発明の効果】【The invention's effect】

(試験例1)インゲン灰色かび病(圃場試験) 試験場所:日本曹達(株)榛原農業研究所 作物 :インゲン豆(品種:さつきみどり2号) 薬剤処理:開花始め期に実施例1に準じて調整した製剤
を所定の薬量に希釈した薬液を、肩掛け式噴霧器で3回
に分けて散布処理した。 発病調査:1区あたり10株の発病程度を以下の発病基
準で調査し、発病度、防除価を算出した。
(Test example 1) Green mold of green beans (field test) Test place: Nippon Soda Co., Ltd., Harabara Agricultural Research Institute Crop: kidney beans (variety: Satsuki Midori No. 2) Chemical treatment: at the beginning of flowering A drug solution prepared by diluting the prepared preparation into a predetermined amount was sprayed with a shoulder sprayer in three times. Disease occurrence survey: The disease severity of 10 strains per ward was investigated according to the following disease criteria, and the disease severity and control value were calculated.

【0016】発病基準と基準値: 発病基準 基準値 発病なし ・・・・・・・・・・ 0 発病箇所 1〜 2個 ・・ 1 発病箇所 3〜 4個 ・・ 2 発病箇所 5〜 9個 ・・ 3 発病箇所 10〜20個 ・・ 4 発病箇所 20個以上 ・・・ 5Crisis standard and standard value: Crisis standard Criterion value No sickness ・ ・ ・ ・ ・ ・ ・ ・ ・ ・ 0 0 1 to 2 spots ・ ・ 1 1 3 to 4 spots ・ 2 2 5 to 9 spots・ ・ 3 10 to 20 diseased spots ・ ・ 4 4 diseased spots 20 or more ・ ・ ・ 5

【0017】[0017]

【数1】 v:発病基準値 n:発病基準(基準値)毎の株数 N:調査株数[Equation 1] v: Disease-causing reference value n: Number of strains for each disease-causing criterion (reference value) N: Number of surveyed strains

【0018】[0018]

【数2】 C:無処理区の発病度 T:試験区の発病度[Equation 2] C: severity of untreated plot T: severity of test plot

【0019】試験結果を表1に示す。The test results are shown in Table 1.

【0020】[0020]

【表1】 [Table 1]

【0021】(試験例2)抗菌試験 直径9cmのシャーレに供試薬剤を所定の濃度となるよう
に添加したジャガイモブドウ糖寒天培地の平板を作製
し、灰色かび病菌(Botrytis cinerea )、菌核病菌(Scl
erotinia sclerotiorum)、キュウリ黒星病菌(Cladospor
ium cucumerinum)を培養し、3〜7日後に生育菌糸直径
を測定し、生育阻害率を算出した。
[0021] (Test Example 2) to produce the added potato dextrose agar plates such petri dish antibacterial test diameter 9cm the test drug at a predetermined concentration, Botrytis cinerea (Botrytis cinerea), Sclerotinia sclerotiorum ( Scl
erotinia sclerotiorum) , cucumber scab (Cladospor)
ium cucumerinum) was cultured, and after 3 to 7 days, the diameter of viable mycelium was measured and the growth inhibition rate was calculated.

【0022】[0022]

【数3】 C:無処理区の菌糸生育直径 T:試験区の菌糸生育直径(Equation 3) C: Mycelial growth diameter of untreated section T: Mycelial growth diameter of test section

【0023】試験結果を表2〜6に示す。The test results are shown in Tables 2-6.

【0024】[0024]

【表2】 [Table 2]

【0025】[0025]

【表3】 [Table 3]

【0026】[0026]

【表4】 [Table 4]

【0027】[0027]

【表5】 [Table 5]

【0028】[0028]

【表6】 [Table 6]

【0029】(試験例3)アブラムシ殺虫試験 予めワタアブラムシを接種した1.3葉期のキュウリ葉
に、実施例1、2に準じて調整した製剤を所定の薬量に
希釈した薬液をクロマト用ガラスノズルで散布処理し
た。処理3日後に成幼虫数を調査し、殺虫率を算出し
た。試験結果を表7に示す。
(Test Example 3) Aphid insecticidal test For a chromatograph, a drug solution prepared by diluting a preparation prepared according to Examples 1 and 2 to a predetermined amount on a 1.3 leaf stage cucumber leaf previously inoculated with cotton aphid was used for chromatography. It was sprayed with a glass nozzle. Three days after the treatment, the number of adult larvae was investigated and the insecticidal rate was calculated. The test results are shown in Table 7.

【0030】[0030]

【表7】 [Table 7]

【0031】(試験例4)ミカンハダニ殺ダニ試験 9cmのシャーレに納めたカンキツ切り取り葉にフェンピ
ラド抵抗性ミカンハダニの雌成虫20匹を接種した。そ
の後実施例2.に準じて調整した製剤を所定の薬量に希
釈した薬液を微量散布装置で散布処理した。処理3日後
にナミハダニの成虫数を調査し、殺虫率を算出した。
Test Example 4 Acaricidal Mite Acaricidal Test Twenty female adults of Fenpyrad-resistant citrus red mite were inoculated into cut citrus leaves placed in a 9 cm petri dish. Then, in Example 2. The drug solution prepared by diluting the preparation prepared in accordance with 1) to a predetermined dose was sprayed with a micro sprayer. After 3 days from the treatment, the number of adults of the spider mite was examined and the insecticidal rate was calculated.

【0032】[0032]

【表8】 [Table 8]

【0033】この試験において、使用した活性化合物間
の相乗効果は、コルビー(R.S.Corby),We
eds.,15,20〜22(1967)の式にて評価
した。
In this test, the synergistic effect between the active compounds used was that of Corby, We.
eds. , 15 , 20 to 22 (1967).

【0034】[0034]

【数5】 ここで、 X=有効成分濃度pの場合の化合物1による防除価 Y=有効成分濃度qの場合の化合物2による防除価 E=p+qの場合の化合物1+2による予想防除価(理
論値)を表す。 観察値が理論値(E)よりも高い場合、この組み合わせ
混合物は相乗作用を有する。
(Equation 5) Here, X = control value by compound 1 in the case of active ingredient concentration p Y = control value by compound 2 in the case of active ingredient concentration q E = predicted control value (theoretical value) by compound 1 + 2 in the case of p + q. If the observed value is higher than the theoretical value (E), this combination mixture has a synergistic effect.

【0035】以上の観察値は、Corbyの理論値
(E)より薬量より高い防除価を示したことから、本発
明の有害生物防除組成物は優れた相乗作用を有すること
が示された。
The above observed values showed a control value higher than the theoretical amount by Corby's theoretical value (E), indicating that the pest control composition of the present invention has an excellent synergistic action.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】N−メチル−(E)−メトキシイミノ[α
−(O−トリロキシ−O−トリル]アセテート、メチル
−(E)−2−{2−[6−(2−シアノフェキシ)ピ
リミジン−4−イルオキシ]フェニール}−3−メトキ
シアクリレート、および(E)−2−メトキシイミノ−
N−メチル−2−(2−フェノキシフェニール)アセタ
ミドからなる群から選ばれる少なくとも1種と、フェン
ピラド、フェンピロキシメートおよびピリダベンからな
る群から選ばれる少なくとも1種とを有効成分として含
有することを特徴とする農園芸用有害生物防除組成物。
1. N-methyl- (E) -methoxyimino [α
-(O-triloxy-O-tolyl] acetate, methyl- (E) -2- {2- [6- (2-cyanophenoxy) pyrimidin-4-yloxy] phenyl} -3-methoxyacrylate, and (E)-. 2-methoxyimino-
It is characterized by containing at least one selected from the group consisting of N-methyl-2- (2-phenoxyphenyl) acetamide and at least one selected from the group consisting of fenpyrad, fenpyroximate and pyridaben, as active ingredients. Agricultural and horticultural pest control composition.
JP7080795A 1995-03-03 1995-03-03 Composition for agricultural and horticultural pest control Pending JPH08245311A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7080795A JPH08245311A (en) 1995-03-03 1995-03-03 Composition for agricultural and horticultural pest control

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7080795A JPH08245311A (en) 1995-03-03 1995-03-03 Composition for agricultural and horticultural pest control

Publications (1)

Publication Number Publication Date
JPH08245311A true JPH08245311A (en) 1996-09-24

Family

ID=13442213

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JPH08245311A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001022818A1 (en) * 1999-09-29 2001-04-05 Basf Corporation Synergistic insecticidal formulations of pyridaben and strobilurins
JP2004345981A (en) * 2003-05-20 2004-12-09 Kumiai Chem Ind Co Ltd Fungicide composition for agriculture and horticulture

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001022818A1 (en) * 1999-09-29 2001-04-05 Basf Corporation Synergistic insecticidal formulations of pyridaben and strobilurins
US6451793B1 (en) 1999-09-29 2002-09-17 Basf Corporation Synergistic insecticidal formulations of pyridaben and strobilurins
KR100707959B1 (en) * 1999-09-29 2007-04-16 롬 앤드 하스 일렉트로닉 머티리얼스 씨엠피 홀딩스 인코포레이티드 Polishing pad
JP2004345981A (en) * 2003-05-20 2004-12-09 Kumiai Chem Ind Co Ltd Fungicide composition for agriculture and horticulture

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