JPS5948807B2 - Acaricide, insecticidal composition - Google Patents

Acaricide, insecticidal composition

Info

Publication number
JPS5948807B2
JPS5948807B2 JP1904178A JP1904178A JPS5948807B2 JP S5948807 B2 JPS5948807 B2 JP S5948807B2 JP 1904178 A JP1904178 A JP 1904178A JP 1904178 A JP1904178 A JP 1904178A JP S5948807 B2 JPS5948807 B2 JP S5948807B2
Authority
JP
Japan
Prior art keywords
mites
results
insecticidal
insecticidal composition
acaricidal
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
Application number
JP1904178A
Other languages
Japanese (ja)
Other versions
JPS54113437A (en
Inventor
忠美 平野
修 多田
正夫 箕輪
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.)
Kumiai Chemical Industry Co Ltd
Original Assignee
Kumiai Chemical Industry 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 Kumiai Chemical Industry Co Ltd filed Critical Kumiai Chemical Industry Co Ltd
Priority to JP1904178A priority Critical patent/JPS5948807B2/en
Publication of JPS54113437A publication Critical patent/JPS54113437A/en
Publication of JPS5948807B2 publication Critical patent/JPS5948807B2/en
Expired legal-status Critical Current

Links

Description

【発明の詳細な説明】 この発明はダニ類および(または)害虫類を防除するた
めの殺ダニ、殺虫組成物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an acaricidal and insecticidal composition for controlling mites and/or pests.

ダニ類はカンキツ類、リンゴ、ナシ等の各種果樹、イチ
ゴ、ナス、スイカ等の野菜類、カーネーション、バラ、
キク等の花卉類、および茶等の葉に寄生加害し、これら
の農作物に多大の被害を4えている。
Mites are found on citrus fruits, various fruit trees such as apples and pears, vegetables such as strawberries, eggplants, and watermelons, carnations, roses, etc.
It parasitizes flowers such as chrysanthemums and leaves of tea plants, causing great damage to these crops.

現在ダニ類の防除にはケルセン、シトラジン、テデオン
、ダニカット、ブリクトラン等の商標のもとに多数の殺
ダニ剤が市販され使用されている。
Currently, a large number of acaricides are commercially available for use in controlling mites under the trademarks of Kelsen, Citrazine, Tedeon, Danicut, Brictran, and the like.

しかしダニ類の一世代の期間は短く、かつ年間の世代回
数も十数世代にのぼる。
However, the generation period of mites is short, and the number of generations per year reaches more than ten.

従って防除回数も多くなり、他の害虫にくらべ抵抗性が
発達しやすく、その防除が大きな問題となっている。
Therefore, the number of times they are controlled is increased, and they are more likely to develop resistance than other pests, making their control a major problem.

そこで抵抗性の発達を回避するため、できる限り同一薬
剤の連用をさけ、作用機構の異なる薬剤のローテーショ
ンによる防除、あるいはそれらの混合剤による防除が考
えられている。
Therefore, in order to avoid the development of resistance, it is considered to avoid repeated use of the same drug as much as possible, and to control by rotating drugs with different mechanisms of action, or by using mixtures thereof.

また前記の各種農作物にはダニ類以外に多くの害虫が寄
生加害するが、ダニ類と混虫類の間には大きな選択毒性
があり、両者に有効な薬剤はほとんどない。
In addition, many pests other than mites parasitize and damage the various agricultural crops mentioned above, but there is a large selective toxicity between mites and mixed insects, and there are almost no drugs that are effective against both.

そのため一般には殺ダニ剤に殺虫剤を混用してダニ類と
害虫の同時防除が行なわれている。
Therefore, acaricides and insecticides are generally used in combination to control mites and pests at the same time.

本発明は特定の薬剤を配合することにより、ダ千類およ
び害虫類の両方に対して相乗的な防除効果を発揮する殺
ダニ、殺虫組成物を提供することを目的とする。
An object of the present invention is to provide an acaricidal and insecticidal composition that exhibits a synergistic control effect against both insects and insect pests by incorporating specific agents.

本発明はS−[(2−メトキシ−5−オキソ−1,3,
4,−チアジアゾリン−4−イル)メチル〕0゜0−ジ
メチルホスホロチオロチオネー)(以下DMTPと称ス
る)と、p−クロロフェニルp−クロロベンゼンスルホ
ネート(以下CPCBSと称する)とを有効成分として
配合したことを特徴とする殺ダニ、殺虫組成物である。
The present invention provides S-[(2-methoxy-5-oxo-1,3,
Contains 4,-thiadiazolin-4-yl)methyl 0゜0-dimethylphosphorothiolothione) (hereinafter referred to as DMTP) and p-chlorophenyl p-chlorobenzenesulfonate (hereinafter referred to as CPCBS) as active ingredients. This is an acaricidal and insecticidal composition characterized by the following.

DMTPは次の(1)式 で表わされ、害虫に対する効力はあるが、ダニ類に対す
る効力は低い。
DMTP is expressed by the following formula (1), and is effective against pests, but has low effectiveness against mites.

CPCBSは次の(2)式 で表わされ、ダニ類に対して物卵、殺成虫力ともある程
度の効力を示すが、害虫に対しては効力を示さない。
CPCBS is expressed by the following formula (2), and exhibits some degree of egg-killing and adult-killing power against mites, but is ineffective against pests.

本発明ではこれらの薬剤を配合することにより、それぞ
れの欠点を相補い、しかも相乗的な殺ダニ、殺虫効果を
発揮させる。
In the present invention, by blending these drugs, the drawbacks of each are compensated for and synergistic acaricidal and insecticidal effects are exerted.

DMTPとCPCBSとの配合比は重量比で1=5〜5
:1の範囲が望ましく、特に1:2〜2:lの範囲がよ
い。
The blending ratio of DMTP and CPCBS is 1=5 to 5 by weight.
A range of :1 is desirable, and a range of 1:2 to 2:1 is particularly preferred.

本発明の殺ダニ、殺虫組成物はこれら2種の有効成分を
混合して製剤することもできるが、これらの有効成分に
さらに担体、稀釈剤、界面活性剤、分散剤、その他の補
助剤等を配合して、水利剤、乳剤、粉剤、フローダスト
等に製剤することができる。
The acaricidal and insecticidal composition of the present invention can be formulated by mixing these two types of active ingredients, but in addition to these active ingredients, carriers, diluents, surfactants, dispersants, other auxiliaries, etc. It can be formulated into aquariums, emulsions, powders, flow dusts, etc.

これらの製剤は直接散布するか、水で適当な濃度に稀釈
して散布し使用する。
These preparations can be sprayed directly or diluted with water to an appropriate concentration and used.

使用濃度は250〜500 ppm で用いると良い効
果が得られる。
Good effects can be obtained when the concentration is 250 to 500 ppm.

担体としてはタルク、カオリン、ベントナイト、ケイソ
ウ土、ホワイトカーボン、クレー、テンプン等、稀釈剤
としては水、キシレン、トルエン、クロロベンゼン、シ
クロヘキサン、アルコール等が使用でき、界面活性剤、
分散剤としては市販のものが使用できる。
As carriers, talc, kaolin, bentonite, diatomaceous earth, white carbon, clay, starch, etc. can be used, as diluents, water, xylene, toluene, chlorobenzene, cyclohexane, alcohol, etc. can be used, and surfactants,
Commercially available dispersants can be used.

本発明の殺ダニ、殺虫組成分は他の殺ダニ剤、殺虫剤、
殺菌剤等と併用することもできる。
The acaricidal and insecticidal components of the present invention are other acaricides, insecticides,
It can also be used in combination with disinfectants and the like.

本発明の殺ダニ、殺虫組成物は相乗的な殺ダニ、殺虫効
果を有し、各有効成分単独使用の場合に比べて顕著な防
除効果を示す。
The acaricidal and insecticidal composition of the present invention has synergistic acaricidal and insecticidal effects, and exhibits a more remarkable control effect than when each active ingredient is used alone.

そしてその効果は長時間持続し、抵抗性が発達しにくい
And the effect lasts for a long time, making it difficult for resistance to develop.

特にノ・ダニ類に対する防除効果は高く、殺卵力、殺成
虫力ともに相乗的に増大する。
In particular, it has a high control effect against insects and mites, and its ovicidal and adulticidal powers increase synergistically.

またカンキツ類のヤノネカイカラムシ、リンゴ、茶のコ
カクモンハマキおよび野菜の・・スモンヨトウ等の害虫
に対しても相乗的に殺虫効力が増大する。
In addition, the insecticidal efficacy is synergistically increased against pests such as citrus lily bugs, apples, tea worms, and vegetables ``spodoptera.''

次に本発明の好適な配合例をあげて説明するが、添加剤
および配合比は広い範囲で変更し5るものである。
Next, preferred blending examples of the present invention will be described, but additives and blending ratios may be varied within a wide range.

なお配合割合はいづれも重量%で示す。配合例 l 水
和剤 DMTP 25%、CPCBS 25%、湿展剤と
してツルポール35 s −L (東邦化学KK答録商
標)3%、ディスクゾールWK(第1工業化学KK登録
商標)3チ、補助剤としてカープレックス(塩野義製薬
KK登録商標)5チ、担体としてラジオライト(昭和化
学KK登録商標)39係を均一に混合粉砕して水利剤と
する。
All blending ratios are expressed in weight %. Formulation example l Wettable powder DMTP 25%, CPCBS 25%, wetting agent Tsurupol 35 s-L (Toho Chemical KK registered trademark) 3%, Discsol WK (Daiichi Kogyo Kagaku KK registered trademark) 3%, auxiliary Carplex (Shionogi & Co., Ltd. KK registered trademark) No. 5 as an agent and Radiolite (Showa Kagaku KK registered trademark) No. 39 as a carrier are uniformly mixed and pulverized to obtain an irrigation agent.

配合例 2 乳 剤 DMTP 25%、CPCBS 25%、稀釈剤と
してキシレン40%、乳化剤としてツルポール3001
10%を均一に溶解して乳剤とする。
Formulation example 2 Emulsion DMTP 25%, CPCBS 25%, xylene 40% as diluent, Trupol 3001 as emulsifier
10% is uniformly dissolved to form an emulsion.

配合例 370−ダスト DMTP 10%、CPCBS 10.%、補助剤
としてイソプロビルハイドロダンホスフェート2%カー
プレックス 30チ、担体としてジ−クライト5G−9
0(ジークライト化学鉱業KK登録商標)48%を混合
微粉砕しフローダストとする。
Formulation example 370-Dust DMTP 10%, CPCBS 10. %, isopropylhydrodanephosphate 2% Carplex 30% as adjuvant, Zikryte 5G-9 as carrier
0 (Ziklite Chemical Mining KK registered trademark) is mixed and pulverized to form flow dust.

次に本発明の殺ダニ、殺虫組成物の効果を試験例により
示す。
Next, the effects of the acaricidal and insecticidal composition of the present invention will be shown by test examples.

供試した薬剤は下記の配合例(重量%)に従って製剤し
た。
The tested drug was formulated according to the following formulation example (% by weight).

試験例 l ニセナミハダニに対する防除効果試験 く ニヤナミハダニの寄生した4寸ポット植えナスに水
利剤の所定濃度(DMTP十CPCBSの濃度以下同じ
)の液50m1をスプレーカンで十分に散布し、経時的
に生息成虫数を調べた。
Test Example 1. Control effect test on black-and-white spider mites. 50 ml of an irrigation agent solution with a prescribed concentration (the same concentration below DMTP and CPCBS) was thoroughly sprayed with a spray can on eggplants planted in 4-inch pots that were infested with white-throated spider mites, and We investigated the number of living adults.

その結果を第1表に示す。The results are shown in Table 1.

なお、比較のために市販の殺ダニ剤ケルtン〔ローム・
アンド・)・−ス社登録商標−有効成分2.2.2−)
リクロローl、1−ビス(p−クロロフェニル)エタノ
ール〕散布オよび無散布の場合の結果も併記する。
For comparison, the commercially available acaricide Kelton [ROHM・
&)・-S Company Registered Trademark-Active Ingredients 2.2.2-)
[Lichlorol, 1-bis(p-chlorophenyl)ethanol] The results with and without spraying are also shown.

試験例 2 ニセナミハダニに対する殺卵効力試験 温室内でインゲンの葉に座下させたニセナミハダニの卵
に乳剤の所定濃度液を1鉢当り30rnl散布t〜 1
0日後に殺卵率を調べた。
Test Example 2 Ovicidal efficacy test against false red spider mite Spraying 30 rnl of emulsion at a predetermined concentration per pot onto the eggs of false red spider mite that have settled on green bean leaves in a greenhouse t ~ 1
The ovicidal rate was examined after 0 days.

その結果を第2表に示すとともに、濃度250 ppm
の場合の配合比−殺卵率のグラフを第1図に示す。
The results are shown in Table 2, and the concentration is 250 ppm.
Figure 1 shows a graph of blending ratio vs. ovicidal rate in the case of .

なお第2表にはケルtン散布の場合の結果も併記する。Table 2 also shows the results in the case of Kelton scattering.

試験例 3 ニセナミ・・ダニに対する殺成虫効力試験温室内でイン
ゲンの葉に寄生させたニセナミハダニ成虫に水和剤の所
定濃度液を1鉢当り30rIll散布し、3日後に生死
虫数を調べ殺ダキ率を算出した。
Test Example 3 Adulticidal efficacy test against false spider mites A 30ml solution of a predetermined concentration of wettable powder per pot was sprayed on adult false spider mites parasitized on green bean leaves in a greenhouse, and the number of living and dead insects was determined after 3 days. Daki rate was calculated.

その結果を第3表に示すとともに、濃度250 ppm
の場合の配合比−殺ダニ率のグラフを第2図に示す。
The results are shown in Table 3, and the concentration is 250 ppm.
A graph of blending ratio vs. acaricidal rate is shown in FIG. 2.

なお第3表にはケルセン散布の場合の結果も併記する。Table 3 also shows the results in the case of Kelsen dispersion.

:試験例 4 ミカン−・ダニに対する防除効果試験 ミカン・・ダニの寄生した4寸ポット植え夏柑実生に水
和剤の所定濃度液50rnlをスプレーガンで十分に散
布し、経時的に生は成虫数を調べた。
: Test Example 4 Mandarin orange - Control effect test against mites Mandarin orange - 50 rnL of a predetermined concentration solution of a hydrating agent was thoroughly sprayed with a spray gun on summer fruit seedlings planted in 4-inch pots that were infested with mites, and over time, the number of live and adult mites increased. I looked up the numbers.

結果を第4表に示す。The results are shown in Table 4.

なおケルセン散布および無散布の場合の結果も併記する
The results with and without Kelsen spraying are also listed.

試験例 5 カンザワハダニに対する防除効果試験 カンザワハダニの寄生している茶樹に水利剤の所定濃度
液を10アール当り400を散布し、散布後経時的に生
息成虫数を調べた。
Test Example 5 Control effect test against Kanzawa spider mite A predetermined concentration solution of an irrigation agent was sprayed at a rate of 400 per 10 ares on tea plants infested with Kanzawa spider mites, and the number of inhabiting adult insects was examined over time after spraying.

結果を第5表に示す。The results are shown in Table 5.

なおケルセン散布および無散布の場合の結果も併記する
The results with and without Kelsen spraying are also listed.

試験例 6 ケルセン抵抗性ナミー・ダニに対する防除効果試験 ケルtン抵抗性ナミハダニを寄生させたりリンゴ実生に
水和剤の所定濃度液50rIxlをスプレーガくンで十
分に散布し、散布後経時的に生息成虫数を調べた。
Test Example 6 Control effect test on Kelsen-resistant two-spotted spider mites Infested with Kelsen-resistant two-spotted spider mites, sufficiently sprayed 50 rIxl of a predetermined concentration of hydrating agent on apple seedlings with a spray gun, and after spraying, the inhabitation occurred over time. The number of adult insects was investigated.

結果を第6表に示す。なおケルセン散布および無散布の
場合の結果も併記する。
The results are shown in Table 6. The results with and without Kelsen spraying are also listed.

試験例 7 コカクモンバマキに対する殺虫効力試験 リンゴの葉を水利剤の所定濃度液に浸漬し、それをアイ
スカップに入れ、そこへコカクモンハマキの3令幼虫を
放ち、72時間後に生死虫数を調べ、殺虫率を求めた。
Test Example 7 Insecticidal Efficacy Test on Kokaku Monbumaki Apple leaves were immersed in a solution of a predetermined concentration of water use agent, placed in an ice cup, and 3rd instar larvae of Kokaku Monbumaki were released there. After 72 hours, the number of live and dead insects was checked to determine the insecticidal rate. I asked for

結果を第7表に示すとともに、濃度250 ppmの場
合の配合比−殺虫率のグラフを第3図に示す。
The results are shown in Table 7, and a graph of blending ratio vs. insecticidal rate at a concentration of 250 ppm is shown in FIG.

なり比較のために市販の殺虫剤サイアノックス(住友化
学工業KK登録商標−有効成分p−シアノフェニルジメ
チルホスホロチオネート)を使用した場合の結果も併記
する。
For comparison, the results obtained using the commercially available insecticide Cyanox (Sumitomo Chemical KK registered trademark - active ingredient p-cyanophenyldimethyl phosphorothionate) are also shown.

試験例 8 ヤノネカイガラに対する殺虫効力試験 ヤノネカイガラ2令幼虫の寄生しているミカンの葉を水
利剤の所定濃度液に浸漬し、無処理区が成虫になったと
き、未成熟成虫、成虫数を調べ次式により発育率を算出
した。
Test Example 8 Insecticidal efficacy test against Yano's Chilling Tit Mandarin orange leaves infested with Yan's Chilling Tit 2nd instar larvae are immersed in a solution of a predetermined concentration of watering agent, and when the untreated plot becomes adults, the number of immature and adult beetles is determined. Growth rate was calculated using the formula.

結果を第8表に示す。成虫数十未成熟成虫数 発育率@)ニ□×100 散布前史数 以上の結果より、ダニ類に対してはDMTP単独の場合
は最初防除効果はあるが、時間の経過とともに急速に効
果が低減し、CPCBS単独の場合は最初からあまり効
果がないのに比べ、両者配合の場合は顕著な防除効果が
あり、その効果が長時間持続することがわかる。
The results are shown in Table 8. 10 Adults Number of immature adults Growth rate @) □ × 100 Based on the results of the pre-distribution number, DMTP alone has an initial control effect against mites, but it rapidly becomes less effective over time. It can be seen that compared to the case where CPCBS alone is not very effective from the beginning, the combination of both has a remarkable pesticidal effect and the effect lasts for a long time.

またその防除効果は両者の配合比が1:5〜5:1の範
囲がよく、2:l〜1:2の範囲が特によいことがわか
る。
It is also found that the pesticidal effect is good when the mixing ratio of both is in the range of 1:5 to 5:1, and particularly in the range of 2:1 to 1:2.

殺虫効果についても両者配合の場合は単独の場合に比べ
顕著な効果を示し、相乗効果が認められる。
As for the insecticidal effect, the combination of the two shows a more pronounced effect than the combination of the two alone, indicating a synergistic effect.

以上本発明を説明したが、本発明の殺ダニ、殺虫組成物
はダニ類、害虫類の両方に対して顕著な防除効果を有し
、その効果の持続性も高い。
The present invention has been described above, and the acaricidal and insecticidal composition of the present invention has a remarkable control effect on both mites and pests, and the effect is highly durable.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は試験例2の濃度250 ppmの場合の配合比
−殺卵率を示すグラフ、第2図は試験例3の濃度250
ppmの場合の配合比−殺ダニ率を示すグラフ、第3
図は試験例7の濃度250 ppmの場合の配合比−殺
虫率を示すグラフである。
Figure 1 is a graph showing the blend ratio vs. ovicidal rate for Test Example 2 at a concentration of 250 ppm, and Figure 2 is a graph showing the ovicidal rate for Test Example 3 at a concentration of 250 ppm.
Graph showing blending ratio vs. acaricidal rate in ppm, 3rd
The figure is a graph showing the blending ratio vs. insecticidal rate in the case of Test Example 7 at a concentration of 250 ppm.

Claims (1)

【特許請求の範囲】 I S−C<2−メトキシ−5−オキソ−1,3゜4
−チアジアゾリン−4−イルツメチル)0,0−ジメチ
ルホスホロチオロチオネートと、p−クロロフェニルp
−クロロベンゼンスルホネートトヲ有効成分として配合
したことを特徴とする殺ダニ、殺虫組成物。 2B−CCメトキシ−5−オキソ−1,3,4−チアジ
アゾリン−4−イル)メチル〕0.0−ジメチルホスホ
ロチオロチオネートとp−クロロフェニルp−クロロペ
ンセンスルホネートの配合比は重量比で1:5〜5:l
である特許請求の範囲第1項記載の組成物
[Claims] I S-C<2-methoxy-5-oxo-1,3°4
-thiadiazolin-4-yltmethyl)0,0-dimethylphosphorothiorothionate and p-chlorophenyl p
- A miticidal and insecticidal composition comprising chlorobenzenesulfonate as an active ingredient. The blending ratio of 2B-CC methoxy-5-oxo-1,3,4-thiadiazolin-4-yl)methyl 0.0-dimethylphosphorothiolothionate and p-chlorophenyl p-chloropensene sulfonate is by weight. 1:5~5:l
The composition according to claim 1, which is
JP1904178A 1978-02-23 1978-02-23 Acaricide, insecticidal composition Expired JPS5948807B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1904178A JPS5948807B2 (en) 1978-02-23 1978-02-23 Acaricide, insecticidal composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1904178A JPS5948807B2 (en) 1978-02-23 1978-02-23 Acaricide, insecticidal composition

Publications (2)

Publication Number Publication Date
JPS54113437A JPS54113437A (en) 1979-09-05
JPS5948807B2 true JPS5948807B2 (en) 1984-11-29

Family

ID=11988332

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1904178A Expired JPS5948807B2 (en) 1978-02-23 1978-02-23 Acaricide, insecticidal composition

Country Status (1)

Country Link
JP (1) JPS5948807B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2632477B2 (en) * 1992-07-13 1997-07-23 本田技研工業 株式会社 Hanger for overhead conveyor for assembling motorcycle bodies

Also Published As

Publication number Publication date
JPS54113437A (en) 1979-09-05

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