JP4529526B2 - Agricultural emulsion - Google Patents

Agricultural emulsion Download PDF

Info

Publication number
JP4529526B2
JP4529526B2 JP2004117573A JP2004117573A JP4529526B2 JP 4529526 B2 JP4529526 B2 JP 4529526B2 JP 2004117573 A JP2004117573 A JP 2004117573A JP 2004117573 A JP2004117573 A JP 2004117573A JP 4529526 B2 JP4529526 B2 JP 4529526B2
Authority
JP
Japan
Prior art keywords
present
polyoxyethylene sorbitan
emulsion
pyriproxyfen
fatty acid
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
JP2004117573A
Other languages
Japanese (ja)
Other versions
JP2005298414A (en
Inventor
敏朗 大坪
尚己 津田
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.)
Sumitomo Chemical Co Ltd
Original Assignee
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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP2004117573A priority Critical patent/JP4529526B2/en
Priority to ZA2004/08240A priority patent/ZA200408240B/en
Priority to ES200402541A priority patent/ES2254014B1/en
Publication of JP2005298414A publication Critical patent/JP2005298414A/en
Application granted granted Critical
Publication of JP4529526B2 publication Critical patent/JP4529526B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

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
    • A01N25/30Biocides, 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 characterised by the surfactants
    • 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings

Landscapes

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

Description

本発明は農薬乳剤、詳しくはピリプロキシフェンを有効成分として含有する農薬乳剤に関する。   The present invention relates to an agrochemical emulsion, and more particularly to an agrochemical emulsion containing pyriproxyfen as an active ingredient.

ピリプロキシフェン[4−フェノキシフェニル (RS)−2−(2−ピリジルオキシ)プロピル エーテル;下式で示される化合物]

Figure 0004529526
が有害生物防除剤の有効成分として知られている(例えば、特許文献1参照)。
一方、硬水で希釈した場合にも乳化安定性が優れる農薬乳剤を得ることは困難な場合があることが知られている。 Pyriproxyfen [4-phenoxyphenyl (RS) -2- (2-pyridyloxy) propyl ether; compound represented by the following formula]
Figure 0004529526
Is known as an active ingredient of a pest control agent (see, for example, Patent Document 1).
On the other hand, it is known that it may be difficult to obtain an agrochemical emulsion having excellent emulsification stability even when diluted with hard water.

特開昭60−215671号公報(製造例2参照)JP-A-60-215671 (see Production Example 2)

本発明は、ピリプロキシフェンを有効成分として含有する農薬乳剤であって、カルシウムイオン又はマグネシウムイオンを多量に含む硬水で希釈した場合でも、乳化安定性に優れる農薬乳剤を提供することを目的とするものである。   An object of the present invention is to provide a pesticidal emulsion containing pyriproxyfen as an active ingredient, which is excellent in emulsion stability even when diluted with hard water containing a large amount of calcium ions or magnesium ions. Is.

本発明者等は、ピリプロキシフェンを有効成分として含有する農薬乳剤であって、硬水で希釈した場合でも乳化安定性に優れる農薬乳剤を提供するために種々検討した結果、芳香族炭化水素を溶剤とし、ポリオキシエチレンソルビタン脂肪酸エステル、及びアルキルアリールスルホン酸塩を含有する農薬乳剤が目的を達することを見出し本発明を完成したものである。   The present inventors have made various studies to provide an agrochemical emulsion containing pyriproxyfen as an active ingredient and having excellent emulsification stability even when diluted with hard water. The present invention has been completed by finding that an agrochemical emulsion containing a polyoxyethylene sorbitan fatty acid ester and an alkylaryl sulfonate achieves its purpose.

即ち、本発明は以下のものである。
1. ピリプロキシフェン、ポリオキシエチレンソルビタン脂肪酸エステル、アルキルアリールスルホン酸塩、及び芳香族炭化水素を含有する農薬乳剤。
2. ピリプロキシフェン1〜15重量%、ポリオキシエチレンソルビタン脂肪酸エステル5〜25重量%、アルキルアリールスルホン酸塩1〜10重量%、及び芳香族炭化水素65〜90重量%を含有する農薬乳剤。
3. ポリオキシエチレンソルビタン脂肪酸エステルがポリオキシエチレンソルビタンC12−18脂肪酸エステルである1.又は2.記載の農薬乳剤。
4. アルキルアリールスルホン酸塩が、アルキルベンゼンスルホン酸塩である1.〜3.いずれか1項記載の農薬乳剤。
That is, the present invention is as follows.
1. An agrochemical emulsion containing pyriproxyfen, polyoxyethylene sorbitan fatty acid ester, alkylaryl sulfonate, and aromatic hydrocarbon.
2. An agrochemical emulsion containing 1-15% by weight of pyriproxyfen, 5-25% by weight of polyoxyethylene sorbitan fatty acid ester, 1-10% by weight of alkylaryl sulfonate, and 65-90% by weight of aromatic hydrocarbons.
3. 1. Polyoxyethylene sorbitan fatty acid ester is polyoxyethylene sorbitan C12-18 fatty acid ester Or 2. The agrochemical emulsion as described.
4). 1. The alkyl aryl sulfonate is an alkyl benzene sulfonate ~ 3. The agrochemical emulsion according to any one of the above.

本発明の農薬乳剤は、硬水で希釈した場合にも乳化安定性に優れるものであり、希釈する水の硬度に関わらず安定した乳化状態の希釈液を得ることができる。   The agrochemical emulsion of the present invention has excellent emulsification stability even when diluted with hard water, and a stable diluted solution in an emulsified state can be obtained regardless of the hardness of the water to be diluted.

本発明の農薬乳剤は、ピリプロキシフェン、ポリオキシエチレンソルビタン脂肪酸エステル、アルキルアリールスルホン酸塩、及び芳香族炭化水素を含有する農薬乳剤である。
本発明の農薬乳剤を構成する各成分の割合は、通常ピリプロキシフェンが1〜15重量%、ポリオキシエチレンソルビタン脂肪酸エステルが5〜25重量%、アルキルアリールスルホン酸塩が1〜10重量%、芳香族炭化水素が65〜90重量%である。
本発明の農薬乳剤は、実質的にピリプロキシフェン、ポリオキシエチレンソルビタン脂肪酸エステル、アルキルアリールスルホン酸塩、及び芳香族炭化水素のみからなるものであってもよく、本発明の効果を損なわない範囲で、更に他の成分が添加されているものであってもよい。
The agrochemical emulsion of the present invention is an agrochemical emulsion containing pyriproxyfen, polyoxyethylene sorbitan fatty acid ester, alkylaryl sulfonate, and aromatic hydrocarbon.
The proportion of each component constituting the agricultural chemical emulsion of the present invention is usually 1-15% by weight of pyriproxyfen, 5-25% by weight of polyoxyethylene sorbitan fatty acid ester, 1-10% by weight of alkylaryl sulfonate, Aromatic hydrocarbon is 65 to 90% by weight.
The agrochemical emulsion of the present invention may be substantially composed of pyriproxyfen, polyoxyethylene sorbitan fatty acid ester, alkylaryl sulfonate, and aromatic hydrocarbon, and does not impair the effects of the present invention. Further, other components may be added.

本発明に用いられるピリプロキシフェンは、例えば特許文献1(特開昭60−215671号公報)に記載された方法で製造することができる。本発明の農薬乳剤には上述の通り、ピリプロキシフェンが通常1〜15重量%含有される。   The pyriproxyfen used in the present invention can be produced, for example, by the method described in Patent Document 1 (Japanese Patent Laid-Open No. 60-215671). As described above, the agrochemical emulsion of the present invention usually contains 1 to 15% by weight of pyriproxyfen.

本発明に用いられるポリオキシエチレンソルビタン脂肪酸エステルとしては、例えばポリオキシエチレンソルビタンC12−16脂肪酸エステルが挙げられる。また、本発明にはポリオキシエチレンソルビタン脂肪酸エステルの中でも入手性の点からポリオキシエチレンソルビタンモノ脂肪酸エステル又はポリオキシエチレンソルビタントリ脂肪酸エステルが好適に用いられる。
本発明に用いられるポリオキシエチレンソルビタン脂肪酸エステルとしては、具体的には例えばモノラウリン酸ポリオキシエチレンソルビタン、モノパルミチン酸ポリオキシエチレンソルビタン、モノステアリン酸ポリオキシエチレンソルビタン、トリステアリン酸ポリオキシエチレンソルビタン、モノオレイン酸ポリオキシエチレンソルビタン、及びトリオレイン酸ポリオキシエチレンソルビタンが挙げられる。
また、本発明には、ポリオキシエチレンソルビタン脂肪酸エステルの中でも、HLBが10.5〜16.5のものが好適に用いられる。
本発明の農薬乳剤には、ポリオキシエチレンスチリルフェニルエーテルが通常5〜25重量%含有される。
Examples of the polyoxyethylene sorbitan fatty acid ester used in the present invention include polyoxyethylene sorbitan C12-16 fatty acid ester. In the present invention, among polyoxyethylene sorbitan fatty acid esters, polyoxyethylene sorbitan mono fatty acid ester or polyoxyethylene sorbitan tri fatty acid ester is preferably used from the viewpoint of availability.
Specific examples of the polyoxyethylene sorbitan fatty acid ester used in the present invention include, for example, polyoxyethylene sorbitan monolaurate, polyoxyethylene sorbitan monopalmitate, polyoxyethylene sorbitan monostearate, polyoxyethylene sorbitan tristearate, Mention may be made of polyoxyethylene sorbitan monooleate and polyoxyethylene sorbitan trioleate.
In the present invention, among polyoxyethylene sorbitan fatty acid esters, those having an HLB of 10.5 to 16.5 are preferably used.
The agrochemical emulsion of the present invention usually contains 5 to 25% by weight of polyoxyethylene styryl phenyl ether.

本発明に用いられるアルキルアリールスルホン酸塩のアルキル基は通常炭素数が8〜15個のアルキル基である。また、アルキルアリールスルホン酸塩の塩としては、例えばナトリウム塩、カリウム塩等のアルカリ金属塩、カルシウム塩、マグネシウム塩等のアルカリ土類金属塩、及びアミン塩が挙げられる。
本発明に用いられるアルキルアリールスルホン酸塩としては、例えばアルキルベンゼンスルホン酸塩が挙げられ、具体的には例えばドデシルベンゼンスルホン酸ナトリウム塩、ドデシルベンゼンスルホン酸カルシウム塩が挙げられる。
本発明の農薬乳剤においては、アルキルアリールスルホン酸塩の量がピリプロキシフェン1重量部に対して通常0.1〜1重量部重量部の範囲内である。また、アルキルアリールスルホン酸塩は、本発明の農薬乳剤に通常1〜10重量%含有される。
The alkyl group of the alkylaryl sulfonate used in the present invention is usually an alkyl group having 8 to 15 carbon atoms. Examples of the salt of alkylaryl sulfonate include alkali metal salts such as sodium salt and potassium salt, alkaline earth metal salts such as calcium salt and magnesium salt, and amine salt.
Examples of the alkyl aryl sulfonate used in the present invention include alkyl benzene sulfonate, and specific examples include sodium dodecyl benzene sulfonate and calcium dodecyl benzene sulfonate.
In the pesticidal emulsion of the present invention, the amount of alkylaryl sulfonate is usually in the range of 0.1 to 1 part by weight with respect to 1 part by weight of pyriproxyfen. The alkylaryl sulfonate is usually contained in the agricultural chemical emulsion of the present invention in an amount of 1 to 10% by weight.

本発明に用いられる芳香族炭化水素としては、例えばトルエン等のアルキルベンゼン、キシレン等のジアルキルベンゼン、メチルナフタレン等のアルキルナフタレン、ジメチルナフタレン等のジアルキルナフタレン、ジメチルモノイソプロピルナフタレン等のトリアルキルナフタレン、及びフェニルキシリルエタンが挙げられる。
本発明には、芳香族炭化水素として市販の溶剤をそのまま用いることもでき、そのような市販の溶剤としては、例えば、ハイゾールSAS−296(1−フェニル−1−キシリルエタンと1−フェニル−1−エチルフェニルエタンの混合物、日本石油株式会社の商品名)、カクタスソルベントHP−MN(メチルナフタレン80%、日鉱石油化学株式会社の商品名)、カクタスソルベントHP−DMN(ジメチルナフタレン80%、日鉱石油化学株式会社の商品名)、カクタスソルベントP−100(炭素数9〜10のアルキルベンゼン、日鉱石油化学株式会社の商品名)、カクタスソルベントP−150(アルキルベンゼン、日鉱石油化学株式会社の商品名)、カクタスソルベントP−180(メチルナフタレンとジメチルナフタレンの混合物、日鉱石油化学株式会社の商品名)、カクタスソルベントP−200(メチルナフタレンとジメチルナフタレンの混合物、日鉱石油化学株式会社の商品名)、カクタスソルベントP−220(メチルナフタレンとジメチルナフタレンの混合物、日鉱石油化学株式会社の商品名)、カクタスソルベントPAD−1(ジメチルモノイソプロピルナフタレン、日鉱石油化学株式会社の商品名)、ソルベッソ100(芳香族炭化水素、エクソン化学株式会社の商品名)、ソルベッソ150(芳香族炭化水素、エクソン化学株式会社の商品名)、ソルベッソ200(芳香族炭化水素、エクソン化学株式会社の商品名)、ULTRA LOW HAPHTHALENE AROMATIC 150(ExxonMobil Chemical Company)、ULTRA LOW NAPHTHALENE AROMATIC 200(ExxonMobil Chemical Company)、スワゾール100(トルエン、丸善石油株式会社の商品名)、及びスワゾール200(キシレン、丸善石油株式会社の商品名)が挙げられる。
芳香族炭化水素は、本発明の農薬乳剤に通常65〜90重量%含有される。
Examples of the aromatic hydrocarbon used in the present invention include alkylbenzene such as toluene, dialkylbenzene such as xylene, alkylnaphthalene such as methylnaphthalene, dialkylnaphthalene such as dimethylnaphthalene, trialkylnaphthalene such as dimethylmonoisopropylnaphthalene, and phenyl. Xylylethane.
In the present invention, a commercially available solvent can be used as it is as an aromatic hydrocarbon. Examples of such a commercially available solvent include Hysol SAS-296 (1-phenyl-1-xylylethane and 1-phenyl-1- Mixture of ethyl phenyl ethane, Nippon Oil Co., Ltd., Cactus Solvent HP-MN (Methylnaphthalene 80%, Nikko Petrochemical Co., Ltd.), Cactus Solvent HP-DMN (Dimethylnaphthalene 80%, Nikko Petrochemical) Cactus Solvent P-100 (alkylbenzene having 9 to 10 carbon atoms, trade name of Nikko Petrochemical Co., Ltd.), Cactus Solvent P-150 (alkylbenzene, trade name of Nikko Petrochemical Co., Ltd.), Cactus Solvent P-180 (Mixture of methylnaphthalene and dimethylnaphthalene Product, trade name of Nikko Petrochemical Co., Ltd.), cactus solvent P-200 (mixture of methylnaphthalene and dimethylnaphthalene, trade name of Nikko Petrochemical Co., Ltd.), cactus solvent P-220 (mixture of methylnaphthalene and dimethylnaphthalene), Product name of Nikko Petrochemical Co., Ltd.), Cactus Solvent PAD-1 (Dimethylmonoisopropylnaphthalene, product name of Nikko Petrochemical Co., Ltd.), Solvesso 100 (Product name of aromatic hydrocarbon, Exxon Chemical Co., Ltd.), Solvesso 150 (Aromatic hydrocarbon, trade name of Exxon Chemical Co., Ltd.), Solvesso 200 (Product name of aromatic hydrocarbon, Exxon Chemical Co., Ltd.), ULTRA LOW HAPHTHALENE AROMATIC 150 (ExxonMobil Chemical Company) , ULTRA LOW NAPHTHALENE AROMATIC 200 (ExxonMobil Chemical Company), Swasol 100 (toluene, Maruzen trade name Oil Corporation), and Swasol 200 (xylene, product name of Maruzen Petrochemical Co., Ltd.) and the like.
Aromatic hydrocarbons are usually contained in the agricultural chemical emulsion of the present invention in an amount of 65 to 90% by weight.

本発明の農薬乳剤は、例えばピリプロキシフェン、ポリオキシエチレンソルビタン脂肪酸エステル、アルキルアリールスルホン酸塩、及び芳香族炭化水素を必要に応じて加熱しながら(80℃以下)均一になるまで攪拌することにより製造することができる。   The agrochemical emulsion of the present invention is stirred, for example, with pyriproxyfen, polyoxyethylene sorbitan fatty acid ester, alkylaryl sulfonate, and aromatic hydrocarbon, while heating as necessary (80 ° C. or less) until uniform. Can be manufactured.

本発明の農薬乳剤は、通常水で希釈して害虫又は害虫が生息する場所に施用される。即ち例えば、本発明の農薬乳剤を10〜5000倍程度に水で希釈して、害虫が生息する植物及び/又は土壌に散布することにより施用される。また、10〜1000倍程度に水で希釈した本発明の農薬乳剤をヘリコプター等で空中散布してもよい。
本発明の農薬乳剤の施用量は、ピリプロキシフェンの量として通常0.1〜1000g/10a、好ましくは1〜100g/10aの割合である。
The agricultural chemical emulsion of the present invention is usually diluted with water and applied to a pest or a place where a pest lives. That is, for example, it is applied by diluting the agrochemical emulsion of the present invention with water about 10 to 5000 times and spraying it on plants and / or soil inhabiting pests. Alternatively, the agrochemical emulsion of the present invention diluted with water to about 10 to 1000 times may be sprayed in the air with a helicopter or the like.
The application amount of the agrochemical emulsion of the present invention is usually 0.1 to 1000 g / 10a, preferably 1 to 100 g / 10a as the amount of pyriproxyfen.

以下、製造例、試験例を挙げて本発明を更に詳しく説明するが、本発明はこれらの例に限定されるものではない。   Hereinafter, the present invention will be described in more detail with reference to production examples and test examples, but the present invention is not limited to these examples.

製造例1
ピリプロキシフェン2.0g、トリオレイン酸ポリオキシエチレンソルビタン(HLB:11、商品名:Alkamuls T85V(Rhodia社製))2.4g、ドデシルベンゼンスルホン酸カルシウム塩0.4g、及びソルベッソ200 15.2gを室温で混合して、本発明の農薬乳剤を得た。
Production Example 1
2.0 g of pyriproxyfen, polyoxyethylene sorbitan trioleate (HLB: 11, trade name: Alkamuls T85V (manufactured by Rhodia)) 2.4 g, calcium dodecylbenzenesulfonate 0.4 g, and Solvesso 200 15.2 g Were mixed at room temperature to obtain the agrochemical emulsion of the present invention.

製造例2
ピリプロキシフェン2.0g、モノオレイン酸ポリオキシエチレンソルビタン(HLB:15、商品名:Alkamuls T80(Rhodia社製))1.2g、ドデシルベンゼンスルホン酸カルシウム塩0.4g、ソルベッソ150 16.4gを室温で混合して、本発明の農薬乳剤を得た。
Production Example 2
2.0 g of pyriproxyfen, 1.2 g of polyoxyethylene sorbitan monooleate (HLB: 15, trade name: Alkamuls T80 (manufactured by Rhodia)), 0.4 g of calcium dodecylbenzenesulfonate, and 16.4 g of Solvesso 150 By mixing at room temperature, the agrochemical emulsion of the present invention was obtained.

製造例3
ピリプロキシフェン2.0g、トリオレイン酸ポリオキシエチレンソルビタン(HLB:11、商品名:Alkamuls T85V(Rhodia社製))2.4g、ドデシルベンゼンスルホン酸カルシウム塩0.4g、及びソルベッソ150 15.2gを室温で混合して、本発明の農薬乳剤を得た。
Production Example 3
2.0 g of pyriproxyfen, polyoxyethylene sorbitan trioleate (HLB: 11, trade name: Alkamuls T85V (manufactured by Rhodia)) 2.4 g, calcium dodecylbenzenesulfonate 0.4 g, and Solvesso 150 15.2 g Were mixed at room temperature to obtain the agrochemical emulsion of the present invention.

製造例4
ピリプロキシフェン2.0g、モノオレイン酸ポリオキシエチレンソルビタン(HLB:15、商品名:Alkamuls T80(Rhodia社製))2.4g、ドデシルベンゼンスルホン酸カルシウム塩0.4g、及びソルベッソ150 15.2gを室温で混合して、本発明の農薬乳剤を得た。
Production Example 4
Pyriproxyfen 2.0 g, monooleic acid polyoxyethylene sorbitan (HLB: 15, trade name: Alkamuls T80 (manufactured by Rhodia)) 2.4 g, calcium dodecylbenzenesulfonate 0.4 g, and Solvesso 150 15.2 g Were mixed at room temperature to obtain the agrochemical emulsion of the present invention.

製造例5
ピリプロキシフェン2.0g、モノオレイン酸ポリオキシエチレンソルビタン(HLB:15、商品名:Alkamuls T80(Rhodia社製))1.2g、ドデシルベンゼンスルホン酸カルシウム塩1.0g、及びソルベッソ150 15.8gを室温で混合して、本発明の農薬乳剤を得た。
Production Example 5
2.0 g of pyriproxyfen, 1.2 g of polyoxyethylene sorbitan monooleate (HLB: 15, trade name: Alkamuls T80 (manufactured by Rhodia)), 1.0 g of calcium dodecylbenzenesulfonate, and 15.8 g of Solvesso 150 Were mixed at room temperature to obtain the agrochemical emulsion of the present invention.

製造例6
ピリプロキシフェン2.0g、モノオレイン酸ポリオキシエチレンソルビタン(HLB:15、商品名:Alkamuls T80(Rhodia社製))2.4g、ドデシルベンゼンスルホン酸カルシウム塩1.0g、及びソルベッソ150 14.6gを室温で混合して、本発明の農薬乳剤を得た。
Production Example 6
Pyriproxyfen 2.0 g, monooleic acid polyoxyethylene sorbitan (HLB: 15, trade name: Alkamuls T80 (manufactured by Rhodia)) 2.4 g, calcium dodecylbenzenesulfonate 1.0 g, and Solvesso 150 14.6 g Were mixed at room temperature to obtain the agrochemical emulsion of the present invention.

製造例7
ピリプロキシフェン2.0g、モノオレイン酸ポリオキシエチレンソルビタン(HLB:15、商品名:Alkamuls T80(Rhodia社製))4.0g、ドデシルベンゼンスルホン酸カルシウム塩1.0g、及びソルベッソ150 13.0gを室温で混合して、本発明の農薬乳剤を得た。
Production Example 7
2.0 g of pyriproxyfen, polyoxyethylene sorbitan monooleate (HLB: 15, trade name: Alkamuls T80 (manufactured by Rhodia)) 4.0 g, 1.0 g of calcium dodecylbenzenesulfonate, and 13.0 g of Solvesso 150 Were mixed at room temperature to obtain the agrochemical emulsion of the present invention.

次に、本発明の農薬乳剤の乳化安定性につき、試験例を示す。
試験例
塩化カルシウム3.04g及び塩化マグネシウム6水和物1.39gを水に溶解し、全量を500mlとして試験用の硬水を調製した。
100mlの栓付きメスシリンダーに前記試験用の硬水95mlを入れ、20℃の恒温水槽にしばらく放置し、水温を20℃に調節した。次いで、上記製造例で得られた本発明の農薬乳剤5mlを該メスシリンダーに加え、2秒間に1回の割合で30回転倒させた後、再び20℃の恒温水槽に1時間放置した。その後、メスシリンダー内の乳化液の状態を観察したところ、本発明の農薬乳剤1〜7について、いずれも均一な乳化状態が保持されているか、クリーム状の分離が1容量%以下であった。
Next, a test example is shown about the emulsion stability of the agrochemical emulsion of this invention.
Test Example Hard water for testing was prepared by dissolving 3.04 g of calcium chloride and 1.39 g of magnesium chloride hexahydrate in water to make the total amount 500 ml.
95 ml of the test hard water was placed in a 100 ml stoppered graduated cylinder and left in a constant temperature water bath at 20 ° C. for a while to adjust the water temperature to 20 ° C. Next, 5 ml of the pesticidal emulsion of the present invention obtained in the above production example was added to the graduated cylinder, tilted 30 times at a rate of once every 2 seconds, and then left again in a constant temperature water bath at 20 ° C. for 1 hour. Thereafter, the state of the emulsified liquid in the graduated cylinder was observed. As for the agricultural chemical emulsions 1 to 7 of the present invention, a uniform emulsified state was maintained or the cream-like separation was 1% by volume or less.

本発明の農薬乳剤は、希釈する水の硬度によらず安定な乳化状態の希釈液を得ることができる。
The agrochemical emulsion of the present invention can provide a stable emulsion in an emulsified state regardless of the hardness of the water to be diluted.

Claims (3)

ピリプロキシフェン1〜15重量%、ポリオキシエチレンソルビタン脂肪酸エステル5〜25重量%、アルキルアリールスルホン酸塩1〜10重量%、及び芳香族炭化水素65〜90重量%を含有する農薬乳剤。An agrochemical emulsion containing 1-15% by weight of pyriproxyfen, 5-25% by weight of polyoxyethylene sorbitan fatty acid ester, 1-10% by weight of alkylaryl sulfonate, and 65-90% by weight of aromatic hydrocarbons. ポリオキシエチレンソルビタン脂肪酸エステルがポリオキシエチレンソルビタンC12−18脂肪酸エステルである請求項1記載の農薬乳剤。2. The agrochemical emulsion according to claim 1, wherein the polyoxyethylene sorbitan fatty acid ester is a polyoxyethylene sorbitan C12-18 fatty acid ester. アルキルアリールスルホン酸塩が、アルキルベンゼンスルホン酸塩である請求項1又は請求項2記載の農薬乳剤。  The agrochemical emulsion according to claim 1 or 2, wherein the alkylaryl sulfonate is an alkylbenzene sulfonate.
JP2004117573A 2004-04-13 2004-04-13 Agricultural emulsion Expired - Fee Related JP4529526B2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP2004117573A JP4529526B2 (en) 2004-04-13 2004-04-13 Agricultural emulsion
ZA2004/08240A ZA200408240B (en) 2004-04-13 2004-10-12 Pesticidal emulsifiable concentrate
ES200402541A ES2254014B1 (en) 2004-04-13 2004-10-25 EMULSIONABLE PESTICID CONCENTRATE.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2004117573A JP4529526B2 (en) 2004-04-13 2004-04-13 Agricultural emulsion

Publications (2)

Publication Number Publication Date
JP2005298414A JP2005298414A (en) 2005-10-27
JP4529526B2 true JP4529526B2 (en) 2010-08-25

Family

ID=35266008

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2004117573A Expired - Fee Related JP4529526B2 (en) 2004-04-13 2004-04-13 Agricultural emulsion

Country Status (3)

Country Link
JP (1) JP4529526B2 (en)
ES (1) ES2254014B1 (en)
ZA (1) ZA200408240B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5202910B2 (en) * 2007-09-05 2013-06-05 住友化学株式会社 Aqueous suspension pesticide composition and method for controlling elution of pesticide active ingredient in microcapsule

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60215671A (en) * 1984-04-10 1985-10-29 Sumitomo Chem Co Ltd Nitrogen-containing heterocyclic compound, its preparation, and noxious life controlling agent containing said compound as active component
JPH1081616A (en) * 1995-12-13 1998-03-31 Sumitomo Chem Co Ltd Shampoo composition
JPH10120502A (en) * 1996-10-22 1998-05-12 Sumitomo Chem Co Ltd Agrochemical composition
JPH10130104A (en) * 1996-11-01 1998-05-19 Sumitomo Chem Co Ltd Agrochemical emulsion
JPH10130103A (en) * 1996-11-01 1998-05-19 Sumitomo Chem Co Ltd Agrochemical composition

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60215671A (en) * 1984-04-10 1985-10-29 Sumitomo Chem Co Ltd Nitrogen-containing heterocyclic compound, its preparation, and noxious life controlling agent containing said compound as active component
JPH1081616A (en) * 1995-12-13 1998-03-31 Sumitomo Chem Co Ltd Shampoo composition
JPH10120502A (en) * 1996-10-22 1998-05-12 Sumitomo Chem Co Ltd Agrochemical composition
JPH10130104A (en) * 1996-11-01 1998-05-19 Sumitomo Chem Co Ltd Agrochemical emulsion
JPH10130103A (en) * 1996-11-01 1998-05-19 Sumitomo Chem Co Ltd Agrochemical composition

Also Published As

Publication number Publication date
ES2254014B1 (en) 2007-08-16
ES2254014A1 (en) 2006-06-01
JP2005298414A (en) 2005-10-27
ZA200408240B (en) 2005-09-28

Similar Documents

Publication Publication Date Title
Tominack et al. Herbicide formulations
JP2018500366A (en) Fungicidal composition
CN1893823A (en) Emulsifiable concentrates containing adjuvants
US10206390B2 (en) Herbicidal suspension concentrate
JP4529526B2 (en) Agricultural emulsion
JP2024504827A (en) Herbicidal compositions, formulations and their applications
JP4543752B2 (en) Agricultural emulsion
CN106102465B (en) Lotion or microemulsion modulation composition
WO2006001415A1 (en) Agricultural-chemical emulsion composition
JP4507661B2 (en) Agricultural emulsion
JP5266638B2 (en) Agricultural emulsion
JP4543729B2 (en) Agricultural emulsion
JP6035239B2 (en) Formulation
JP4534562B2 (en) Agricultural emulsion
JP4561131B2 (en) Agricultural emulsion
JP4543738B2 (en) Agricultural emulsion
JP5040251B2 (en) Pyridalyl emulsion
JP2006143706A (en) Agrochemical emulsion
UA128533C2 (en) R-type pyridyloxycarboxylic acid, salt and ester derivative thereof, and preparation method therefor, and herbicidal composition and application thereof
DK179289B1 (en) Liquid agrochemical
JP2007269781A (en) Agrochemical emulsifiable concentrate
JP2006527745A5 (en)
JP4216517B2 (en) Liquid composition for pest control
JPH01110604A (en) Control of harmful weed
JP2001048702A (en) Insecticide composition

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20070227

RD05 Notification of revocation of power of attorney

Free format text: JAPANESE INTERMEDIATE CODE: A7425

Effective date: 20080130

RD05 Notification of revocation of power of attorney

Free format text: JAPANESE INTERMEDIATE CODE: A7425

Effective date: 20080513

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20100323

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20100422

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20100518

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20100531

R151 Written notification of patent or utility model registration

Ref document number: 4529526

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R151

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130618

Year of fee payment: 3

LAPS Cancellation because of no payment of annual fees