JPH0759481B2 - Stable pesticide formulation in water - Google Patents

Stable pesticide formulation in water

Info

Publication number
JPH0759481B2
JPH0759481B2 JP58211554A JP21155483A JPH0759481B2 JP H0759481 B2 JPH0759481 B2 JP H0759481B2 JP 58211554 A JP58211554 A JP 58211554A JP 21155483 A JP21155483 A JP 21155483A JP H0759481 B2 JPH0759481 B2 JP H0759481B2
Authority
JP
Japan
Prior art keywords
water
weight
spraying
pesticide
parts
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 - Lifetime
Application number
JP58211554A
Other languages
Japanese (ja)
Other versions
JPS60104002A (en
Inventor
国男 川畑
純隆 古瀬
正一 柴山
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.)
Nihon Nohyaku Co Ltd
Original Assignee
Nihon Nohyaku 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 Nihon Nohyaku Co Ltd filed Critical Nihon Nohyaku Co Ltd
Priority to JP58211554A priority Critical patent/JPH0759481B2/en
Priority to FR848416997A priority patent/FR2554683B1/en
Priority to GB08428211A priority patent/GB2149665B/en
Priority to AU35210/84A priority patent/AU560953B2/en
Priority to HU844183A priority patent/HU199233B/en
Priority to KR1019840007017A priority patent/KR850003656A/en
Priority to PH31432A priority patent/PH20054A/en
Priority to CN85100808.9A priority patent/CN1004605B/en
Publication of JPS60104002A publication Critical patent/JPS60104002A/en
Priority to HK531/92A priority patent/HK53192A/en
Publication of JPH0759481B2 publication Critical patent/JPH0759481B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/02Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
    • A01N25/04Dispersions, emulsions, suspoemulsions, suspension concentrates or gels

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Plant Pathology (AREA)
  • Toxicology (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

【発明の詳細な説明】 本発明は安定な水中懸濁状農薬製剤に関するものであ
る。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to stable pesticide formulations in water.

更に詳しくは、本発明は特殊な界面活性剤及び水溶性増
粘剤であるヘテロポリサッカライドを配合することによ
り、水中懸濁状農薬製剤が均一分散性を長期にわたって
保持し、地上散布の通常濃度散布は勿論のこと、航空散
布(ULV散布、LV散布及びS散布)等の高濃度散布にも
適し、更にかかる高濃度散布に於いても他の農薬乳剤と
の混合使用が可能な水中懸濁状農薬製剤を提供するもの
である。
More specifically, the present invention mixes a special surfactant and a heteropolysaccharide which is a water-soluble thickener to maintain a uniform dispersibility of a pesticide formulation in water for a long period of time, and to apply it at a normal concentration for ground spraying. Of course, it is also suitable for high-concentration spraying such as aviation spraying (ULV spraying, LV spraying and S spraying), and even in such high-concentration spraying, it can be mixed with other agricultural chemical emulsions and suspended in water. It provides pesticide formulations.

農薬の製剤形体としては一般に、粉剤、粒剤、水和剤及
び乳剤がある。これらのうち、粉剤は散布の際に周囲へ
の飛散が多いなどの欠点を有する。又、水和剤は微粒子
からなるために散布液調製時の粉立ちがひどく、人体へ
の影響が問題となる。更に、乳剤は原体が有機溶媒に容
易に溶解する必要があるために、乳剤化できる農薬原体
が限られること及び有機溶媒を用いるために貯蔵時の危
険性があること、ならびに作物によっては薬害を招来す
ること等の欠点を有する。
Pesticide formulation forms generally include powders, granules, wettable powders and emulsions. Among these, the dust has a drawback that it is often scattered to the surroundings during spraying. In addition, since the wettable powder is composed of fine particles, powdering during preparation of the spray liquid is severe, which causes a problem of affecting the human body. In addition, emulsions require that the drug substance be readily soluble in organic solvents, which limits the pesticide drug substance that can be emulsified and the risk of storage due to the use of organic solvents, and in some crops. It has drawbacks such as chemical damage.

更に、最近は散布作業の省力化を図るために、液剤によ
る航空散布(ULV散布、LV散布及びS散布)等が広く普
及しているが、従来の剤型は必ずしもこれに適している
とはいえず、新しい剤型の製剤開発が望まれている。こ
れに適した製剤として、水に難溶又は不溶の固体原体の
微細粒子を乳化剤及び分散剤の添加により水又は親水性
溶媒中に懸濁状に製剤した散布剤が知られている。
Furthermore, recently, in order to save labor in the spraying work, air spraying with liquid agents (ULV spraying, LV spraying and S spraying) has become widespread, but conventional dosage forms are not always suitable for this. No, the development of new drug formulations is desired. As a suitable formulation for this, a spraying agent is known in which fine particles of a solid raw material which is poorly soluble or insoluble in water are formulated in a suspension form in water or a hydrophilic solvent by adding an emulsifier and a dispersant.

しかしながら、従来の懸濁状製剤は長期的物理安定性に
乏しく、更に高濃度散布である航空散布に於いて他の乳
剤との混合使用により懸濁粒子の凝集が起り、分離、沈
降して、ヘリコプターのストレーナーをつまらせたり、
凝集物が作物に付着することにより薬害をひきおこす等
の欠点があり、懸濁状農薬製剤に適した特性有していな
い。
However, conventional suspension-type preparations have poor long-term physical stability, and in aerial spraying, which is a high-concentration spray, when mixed with other emulsions, agglomeration of suspended particles occurs, causing separation and sedimentation. Squeeze a helicopter strainer,
It has drawbacks such as the chemical damage caused by the agglomerates adhering to crops, and it does not have properties suitable for pesticide formulations in suspension.

特開昭55−129201号公報、特公昭58−24401号公報及び
特開昭58−124702号公報には懸濁型農薬製剤の技術が開
示されているが特開昭55−129201号公報記載の製剤で
は、有効成分である水に難溶又は水に不溶の農薬が十分
水中に湿展せずに均一に懸濁しないし、他の農薬乳剤と
混合使用した場合凝集物が生成しストレーナをつまらせ
る原因となる。
JP-A-55-129201, JP-B-58-24401 and JP-A-58-124702 disclose the technology of a suspension-type agrochemical formulation, but it is described in JP-A-55-129201. In the formulation, the active ingredient sparingly water-soluble or water-insoluble pesticide does not sufficiently spread in water and does not suspend uniformly, and when used in combination with other pesticide emulsions, agglomerates are formed and the strainer is blocked. Cause.

特公昭58−24401号公報記載の製剤では降伏値が悪いた
めに長期保存安定性が悪いという欠点を有する。又、特
開昭58−124702号公報記載の製剤では他の農薬乳剤と混
合して使用できない。即ち、同時期に発生する病害虫を
防除するために、省力的手段として現場で他の農薬と混
合して散布する方法が用いられているが、使用する他の
農薬乳剤と混合した際にクリーム状の凝集物が生成し、
これがストレーナをつまらせる原因となる。
The formulation described in Japanese Patent Publication No. 58-24401 has a drawback that the long-term storage stability is poor because the yield value is poor. Further, the formulation described in JP-A-58-124702 cannot be used as a mixture with other agricultural chemical emulsions. That is, in order to control pests that occur at the same time, a method of mixing and spraying with other pesticides is used as a labor-saving means in the field. Agglomerates of
This causes the strainer to jam.

本発明者等は上記の欠点を解消すべく鋭意研究を重ねた
結果、特殊な乳化剤及びヘテロポリサッカライドを配合
することにより常温で固体かつ水難溶性又は水不溶性の
農薬を均一、かつ安定に水中に懸濁させ、取扱いが容易
で貯蔵安定性、散布時の分散性及び懸水性に優れ、航空
散布にも適用可能であり、かつ他の農薬乳剤との混合使
用が可能な水中懸濁状農薬製剤を発明したものである。
The present inventors have conducted extensive studies to eliminate the above drawbacks, and as a result, by blending a special emulsifier and a heteropolysaccharide, a pesticide that is solid and sparingly water-soluble or water-insoluble at room temperature is uniformly and stably suspended in water. A pesticide formulation in suspension in water that is turbid, easy to handle, has excellent storage stability, dispersibility during spraying and excellent water suspension properties, is applicable to aerial spraying, and can be mixed with other pesticide emulsions. It was invented.

即ち、本発明の水中懸濁状農薬製剤は、常温で固体かつ
水難溶性又は水不溶性の農薬の一種以上を50重量%以
下、ポリオキシエチレンアルキルフェノールエーテルを
0.1乃至5.0重量%、ポリオキシエチレンアルキルフエノ
ールエーテルホルマリン縮合物又はポリオキシエチレン
スチレン化フェノールエーテルから選ばれる一種以上の
非イオン型界面活性剤を0.1乃至5.0重量%及び25℃にお
ける降伏値が10dyne/cm2以上になる様にヘテロポリサッ
カライドを充分存在せしめてなり、かつ、他の農薬乳剤
と混合使用が可能であることを特徴とする。
That is, the water-based pesticide formulation of the present invention is 50 wt% or less of one or more solid and sparingly water-soluble or water-insoluble pesticide at room temperature, polyoxyethylene alkylphenol ether
0.1 to 5.0% by weight, 0.1 to 5.0% by weight of one or more nonionic surfactants selected from polyoxyethylene alkylphenol ether formalin condensate or polyoxyethylene styrenated phenol ether, and the yield value at 25 ° C. is 10 dyne / It is characterized in that the heteropolysaccharide is sufficiently present so as to have a cm 2 or more, and that it can be used as a mixture with other agricultural chemical emulsions.

本発明で使用できる農薬としては、2−t−ブチルイミ
ノ−3−イソプロピル−5−フェニル−3,4,5,6−テト
ラハイドロ−2H−1,3,5−チアジアジン−4−オン〔一
般名ブプロフェジン〕及び/又は3′−イソプロポキシ
−2−トリフルオロトルアニリド〔一般名フルトラニ
ル〕が挙げられる。
Examples of pesticides that can be used in the present invention include 2-t-butylimino-3-isopropyl-5-phenyl-3,4,5,6-tetrahydro-2H-1,3,5-thiadiazin-4-one [general name Buprofezin] and / or 3′-isopropoxy-2-trifluorotoluanilide [generic name flutolanil].

これらの農薬は単独で用いても良く、混合して用いても
良い。
These pesticides may be used alone or in combination.

上記農薬の配合割合は50重量%以下、好ましくは10乃至
50重量%である。
The content ratio of the above-mentioned pesticide is 50% by weight or less, preferably 10 to
50% by weight.

本発明で使用するポリオキシエチレンアルキルフェノー
ルエーテルとしてはポリオキシエチレンノニルフェノー
ルエーテル等が使用でき、その配合割合は0.1乃至5.0重
量%、好ましくは0.1乃至3重量%である。
As the polyoxyethylene alkylphenol ether used in the present invention, polyoxyethylene nonylphenol ether and the like can be used, and the compounding ratio thereof is 0.1 to 5.0% by weight, preferably 0.1 to 3% by weight.

非イオン型界面活性剤としては、ポリオキシエチレンア
ルキルフェノールエーテルホルマリン縮合物又はポリオ
キシエチレンスチレン化フェノールエーテルから選ばれ
る1種以上のものを配合すれば良い。これらの界面活性
剤は単独で使用しても良く又混合して使用しても良い。
As the nonionic surfactant, one or more kinds selected from polyoxyethylene alkylphenol ether formalin condensate or polyoxyethylene styrenated phenol ether may be blended. These surfactants may be used alone or in combination.

非イオン型界面活性剤の配合割合は0.1乃至5.0重量%の
範囲から適宜選択することができる。
The blending ratio of the nonionic surfactant can be appropriately selected from the range of 0.1 to 5.0% by weight.

ヘテロポリサッカライドは水溶性増粘剤として配合され
るものであり、一般にキサンタンガム(Xanthan gum)
と呼ばれ、キサントモナス属のバクテリア作用で製造さ
れる高分子量の線状細胞外物質である。このものは分子
量200,000を超え、好ましくは1,000,000以上の分子量を
有する。ヘテロポリサッカライドの配合割合は、懸濁状
農薬製剤の25℃における降伏値が10dyne/cm2以上となる
に充分な量配合すれば良く、好ましくは0.05乃至0.5重
量%である。農薬製剤の降伏値が10dyne/cm2以下である
様なキサンタンガムの添加量では、有効成分が沈降し
て、再分散が困難となり物理的安定性において問題とな
る。
Heteropolysaccharides are used as water-soluble thickeners and are generally used as xanthan gum.
It is a high molecular weight linear extracellular substance produced by the bacterial action of the genus Xanthomonas. It has a molecular weight of more than 200,000, preferably 1,000,000 or more. The heteropolysaccharide may be blended in an amount sufficient to yield a yield value at 25 ° C. of the agricultural chemical preparation in suspension of 10 dyne / cm 2 or more, preferably 0.05 to 0.5% by weight. When the amount of xanthan gum added is such that the yield value of the pesticide formulation is 10 dyne / cm 2 or less, the active ingredient precipitates, redispersion becomes difficult, and physical stability becomes a problem.

本発明の水中懸濁状農薬製剤に使用する溶媒としては、
水が主体となり、水単独でもよいが、必要によりメチル
アルコール、エチルアルコール、イソプロピルアルコー
ル、ポリエチレングリコール、エチレングリコール、プ
ロピレングリコール等の親水性溶媒、又は場合によって
はキシレン、トルエン、ケロシン、鉱油、植物油、流動
パラフィン等の疎水性溶媒から選ばれる一種以上の有機
溶媒を配合しても良い。有機溶媒を配合する場合1乃至
30重量%、好ましくは10乃至20重量%が良い。
The solvent used in the waterborne pesticide formulation of the present invention,
Mainly water, may be water alone, if necessary, a hydrophilic solvent such as methyl alcohol, ethyl alcohol, isopropyl alcohol, polyethylene glycol, ethylene glycol, propylene glycol, or in some cases xylene, toluene, kerosene, mineral oil, vegetable oil, One or more organic solvents selected from hydrophobic solvents such as liquid paraffin may be blended. When blending an organic solvent 1 to
30% by weight, preferably 10 to 20% by weight.

本発明は上記成分のほかに、必要に応じて5重量%以下
の消泡剤、例えばジメチルポリシロキサンを主成分とす
るシリコーン系消泡剤等を配合しても良く、又農薬原体
の粉砕助剤として5重量%以下の親水性シリカ等を必要
に応じて配合しても良く、更に必要に応じて他の成分を
配合しても良い。又、本発明の水中懸濁状農薬と混合し
て使用できる他の農薬としてはMEP乳剤、BPMC乳剤、MEP
・BPMC乳剤、ダイアジノン乳剤、PAP乳剤、イソプロチ
オラン乳剤、マラソン乳剤、IBP乳剤等を挙げることが
できるが本発明はこれらに限定されるものではない。
In the present invention, in addition to the above components, if necessary, 5% by weight or less of an antifoaming agent, for example, a silicone antifoaming agent containing dimethylpolysiloxane as a main component may be blended. As an auxiliary agent, 5% by weight or less of hydrophilic silica or the like may be blended if necessary, and further, other components may be blended if necessary. Other pesticides that can be used as a mixture with the pesticide suspension in water of the present invention include MEP emulsion, BPMC emulsion, MEP emulsion.
-BPMC emulsion, diazinon emulsion, PAP emulsion, isoprothiolane emulsion, marathon emulsion, IBP emulsion and the like can be mentioned, but the present invention is not limited thereto.

本発明の製造工程の一例を示すと、例えばポリオキシエ
チレンアルキルフェノールエーテル、非イオン型界面活
性剤及び必要に応じて消泡剤、有機溶媒の所定量を撹拌
機により水に懸濁又は溶解させ、次いで有効成分を加
え、これらの混合物を湿式粉砕機により、有効成分が5
μm以下、好ましくは0.5乃至3.0μmになるように微粉
砕し、次いで所定量のヘテロポリサッカライドを入れ、
均一に混合して製品を得る。
As an example of the production process of the present invention, for example, polyoxyethylene alkylphenol ether, a nonionic surfactant and optionally a defoaming agent, a predetermined amount of an organic solvent is suspended or dissolved in water by a stirrer, The active ingredients are then added and the mixture is wet milled to give
Finely pulverized to a size of less than or equal to μm, preferably 0.5 to 3.0 μm, and then adding a predetermined amount of heteropolysaccharide,
Mix evenly to obtain the product.

次に本発明の実施例及び試験例を示す。尚、各例中部と
あるのは重量部を示す。
Next, examples and test examples of the present invention will be shown. In addition, "parts in each example" means "parts by weight".

実施例1 ブプロフェジン 42.00部 ポリオキシエチレン(10モル)ノニルフェノールエーテ
ル 1.40部 ポリオキシエチレン(24モル)スチレン化フェノールエ
ーテル 2.00部 プロピレングリコール 3.00部 消泡剤 0.50部 ヘテロポリサッカライド 0.15部 親水性シリカ 3.00部 水 47.95部 水47.95部にポリオキシエチレン(10モル)ノニルフェ
ノールエーテル1.40部、ポリオキシエチレン(24モル)
スチレン化フェノールエーテル2.00部、プロピレングリ
コール3.00部及び消泡剤0.50部(シリコーンKM−73、信
越化学工業株式会社製)を加え、通常撹拌機(ホモミキ
サーHV−M型、特殊機化工業株式会社製)により20分間
溶解混合し、次にブプロフェジン42.0部及び親水性シリ
カ(カープレックス#80、塩野義製薬株式会社)を加
え、湿式粉砕機(アトライター;株式会社三井三池製作
所製)にて3時間微粉砕を行った。更にヘテロポリサッ
カライド0.15部を加え、20分間混合して均一な製剤100
部を得た。
Example 1 Buprofezin 42.00 parts Polyoxyethylene (10 mol) Nonylphenol ether 1.40 parts Polyoxyethylene (24 mol) Styrenated phenol ether 2.00 parts Propylene glycol 3.00 parts Defoamer 0.50 parts Heteropolysaccharide 0.15 parts Hydrophilic silica 3.00 parts Water 47.95 Parts Polyoxyethylene (10 mol) nonylphenol ether 1.40 parts, polyoxyethylene (24 mol) in 47.95 parts of water
Add 2.00 parts of styrenated phenol ether, 3.00 parts of propylene glycol and 0.50 parts of antifoaming agent (Silicone KM-73, manufactured by Shin-Etsu Chemical Co., Ltd.) and add a regular stirrer (Homomixer HV-M type, Tokushu Kika Kogyo Co., Ltd.). 20) for 20 minutes, and then 42.0 parts of buprofezin and hydrophilic silica (Carplex # 80 , Shionogi Pharmaceutical Co., Ltd.) are added, and the mixture is mixed with a wet pulverizer (attritor; Mitsui Miike Seisakusho Co., Ltd.) Milled for hours. Add 0.15 parts of heteropolysaccharide and mix for 20 minutes to obtain a uniform preparation 100
I got a part.

同様にして実施例2乃至9、参考例1乃至10、及び実施
例10乃至12並びに参考例11乃至15の製剤を調製した。そ
の処方を第1表、第2表及び第3表に示す。
Similarly, the formulations of Examples 2 to 9, Reference Examples 1 to 10, Examples 10 to 12 and Reference Examples 11 to 15 were prepared. The prescriptions are shown in Table 1, Table 2 and Table 3.

試験例1 実施例及び参考例により得られた製剤について粘度(見
掛粘度及び降伏値)及び物理的静置安定性(沈降容積
比)を次の方法により測定した。
Test Example 1 The viscosity (apparent viscosity and yield value) and physical standing stability (sedimentation volume ratio) of the preparations obtained in Examples and Reference Examples were measured by the following methods.

粘度:E型粘度計(東京計器製作所製)を用い、25℃に品
温を保ち測定する。
Viscosity: Using an E-type viscometer (manufactured by Tokyo Keiki Seisakusho Co., Ltd.), keep the product temperature at 25 ° C and measure.

使用コーンは1度34分コーン。The corn used is 1 34 minutes corn.

見掛粘度は、ずり速度100sec-1における粘度。The apparent viscosity is the viscosity at a shear rate of 100 sec -1 .

降伏値はずり速度0sec-1におけるずり応力にて示した。Yield value Shear stress at shear rate 0 sec -1 is shown.

沈降容積比:内径1.3cm、容量20mlの共栓付メスシリン
ダーに本発明製剤又は比較例製剤20mlを入れ、40℃恒温
槽に1ケ月静置する。静置後の懸濁層の占める容量Vml
を測定し、全容積に対するこの懸濁層の占める割合を沈
降容積比として下記の式により求める。
Sedimentation volume ratio: 20 ml of the preparation of the present invention or the preparation of the comparative example is put into a measuring cylinder with an internal diameter of 1.3 cm and a capacity of 20 ml, and the mixture is left to stand in a thermostat at 40 ° C for 1 month. Volume of suspended layer after standing Vml
Is measured, and the ratio of this suspension layer to the total volume is determined as the sedimentation volume ratio by the following formula.

この値を物理的静置安定性の指数とする。This value is used as an index of physical static stability.

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

試験例2 混用試験 500mlの広口瓶に水を入れ、次に所定量の市販乳剤を入
れ、良く撹拌し均一乳化、分散させる。次に所定量の本
発明製剤を入れ、均一に分散させて、LV散布(1ヘクタ
ール当り8)に相当する希釈濃度の混合薬液を調整す
る。この薬液を2時間静置した後、250メッシュのスト
レーナーを通過させストレーナー上の残査の量及び性状
から混合使用の可否を調査した。
Test Example 2 Mixing test Water is put in a 500 ml wide-mouthed bottle, and then a predetermined amount of a commercially available emulsion is put therein, and well stirred to uniformly emulsify and disperse. Next, a predetermined amount of the preparation of the present invention is added and uniformly dispersed to prepare a mixed drug solution having a dilution concentration corresponding to LV spraying (8 per hectare). After allowing this chemical solution to stand for 2 hours, it was passed through a strainer of 250 mesh, and the possibility of mixing and using was investigated from the amount and properties of the residue on the strainer.

○:残査なし 混合使用可 ×:クリーム状残査有り 混合使用不可 結果を第5表に示す。○: No residue, mixed use possible ×: Creamy residue, no mixed use results are shown in Table 5.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】2−t−ブチルイミノ−3−イソプロピル
−5−フェニル−3,4,5,6−テトラハイドロ−2H−1,3,5
−チアジアジン−4−オン及び/又は3′−イソプロポ
キシ−2−トリフルオロトルアニリドを10乃至50重量
%、ポリオキシエチレンアルキルフェノールエーテルを
0.1乃至5.0重量%、ポリオキシエチレンアルキルフェノ
ールエーテルホルマリン縮合物又はポリオキシエチレン
スチレン化フェノールエーテルから選ばれる一種以上の
非イオン型界面活性剤を0.1乃至5.0重量%及び25℃にお
ける降伏値が10dyne/cm2以上になる様にヘテロポリサッ
カライドを充分存在せしめてなり、かつ、他の農薬乳剤
と混合使用が可能であることを特徴とする安定なる水中
懸濁状農薬製剤。
1. 2-t-Butylimino-3-isopropyl-5-phenyl-3,4,5,6-tetrahydro-2H-1,3,5
-Thiadiazin-4-one and / or 3'-isopropoxy-2-trifluorotoluanilide 10 to 50% by weight, polyoxyethylene alkylphenol ether
0.1 to 5.0% by weight, 0.1 to 5.0% by weight of one or more nonionic surfactants selected from polyoxyethylene alkylphenol ether formalin condensate or polyoxyethylene styrenated phenol ether, and the yield value at 25 ° C is 10 dyne / cm. A stable pesticide formulation in water, characterized in that the heteropolysaccharide is sufficiently present so as to be 2 or more, and can be mixed with other pesticide emulsions.
JP58211554A 1983-11-10 1983-11-10 Stable pesticide formulation in water Expired - Lifetime JPH0759481B2 (en)

Priority Applications (9)

Application Number Priority Date Filing Date Title
JP58211554A JPH0759481B2 (en) 1983-11-10 1983-11-10 Stable pesticide formulation in water
FR848416997A FR2554683B1 (en) 1983-11-10 1984-11-08 STABILIZED AQUEOUS PESTICIDE SUSPENSION CONCENTRATE
GB08428211A GB2149665B (en) 1983-11-10 1984-11-08 Stabilized aqueous pesticidal suspension concentrate
AU35210/84A AU560953B2 (en) 1983-11-10 1984-11-08 Pesticidal suspension concentrate
KR1019840007017A KR850003656A (en) 1983-11-10 1984-11-09 Stable Underwater Pesticides
HU844183A HU199233B (en) 1983-11-10 1984-11-09 Stabilized aqueous pesticidal suspension concentrate
PH31432A PH20054A (en) 1983-11-10 1984-11-09 Stabilized aqueous pesticidal suspension concentrate
CN85100808.9A CN1004605B (en) 1983-11-10 1985-04-01 Stable suspending concentrate of aqueous pesticide
HK531/92A HK53192A (en) 1983-11-10 1992-07-16 Stabilized aqueous pesticidal suspension concentrate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58211554A JPH0759481B2 (en) 1983-11-10 1983-11-10 Stable pesticide formulation in water

Publications (2)

Publication Number Publication Date
JPS60104002A JPS60104002A (en) 1985-06-08
JPH0759481B2 true JPH0759481B2 (en) 1995-06-28

Family

ID=16607731

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58211554A Expired - Lifetime JPH0759481B2 (en) 1983-11-10 1983-11-10 Stable pesticide formulation in water

Country Status (9)

Country Link
JP (1) JPH0759481B2 (en)
KR (1) KR850003656A (en)
CN (1) CN1004605B (en)
AU (1) AU560953B2 (en)
FR (1) FR2554683B1 (en)
GB (1) GB2149665B (en)
HK (1) HK53192A (en)
HU (1) HU199233B (en)
PH (1) PH20054A (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2764270B2 (en) * 1988-05-10 1998-06-11 日本農薬株式会社 Stable aqueous suspension pesticide composition
US5496845A (en) * 1994-05-25 1996-03-05 American Cyanamid Co. Suspension concentrate compositions of arylpyrrole insecticidal and acaricidal agents
PL318439A1 (en) * 1994-08-03 1997-06-09 Zeneca Ltd Gel-type preparation
JP3600670B2 (en) * 1995-12-08 2004-12-15 アグロカネショウ株式会社 Pesticide aqueous suspension composition and containered pesticide aqueous suspension composition
GB2432119B (en) * 2005-11-10 2011-03-23 Biotech Internat Ltd Improvements in and relating to biocidal compositions
CN101554163B (en) * 2008-04-08 2012-12-12 中国农业科学院农业环境与可持续发展研究所 Pesticide adjuvant and preparation method thereof
MY171459A (en) * 2012-06-06 2019-10-15 Dow Agrosciences Llc High strength herbicidal suspension concentrates
US10463045B2 (en) * 2015-09-30 2019-11-05 Nippon Soda Co., Ltd. Agrochemical composition

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3948636A (en) * 1972-11-09 1976-04-06 Diamond Shamrock Corporation Flowable aqueous composition of water-insoluble pesticide
JPS55129201A (en) * 1979-03-28 1980-10-06 Kao Corp Fluid pesticidal composition
JPS5758601A (en) * 1980-09-25 1982-04-08 Toho Chem Ind Co Ltd Suspension of agricultural chemical

Also Published As

Publication number Publication date
CN85100808A (en) 1987-01-10
CN1004605B (en) 1989-06-28
PH20054A (en) 1986-09-18
FR2554683B1 (en) 1990-06-08
GB2149665B (en) 1987-07-22
GB8428211D0 (en) 1984-12-19
JPS60104002A (en) 1985-06-08
HUT36982A (en) 1985-11-28
KR850003656A (en) 1985-06-26
FR2554683A1 (en) 1985-05-17
AU560953B2 (en) 1987-04-30
HU199233B (en) 1990-02-28
HK53192A (en) 1992-07-24
GB2149665A (en) 1985-06-19
AU3521084A (en) 1985-05-16

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