JP2002114613A - Pest control agent for septic tank - Google Patents
Pest control agent for septic tankInfo
- Publication number
- JP2002114613A JP2002114613A JP2000307405A JP2000307405A JP2002114613A JP 2002114613 A JP2002114613 A JP 2002114613A JP 2000307405 A JP2000307405 A JP 2000307405A JP 2000307405 A JP2000307405 A JP 2000307405A JP 2002114613 A JP2002114613 A JP 2002114613A
- Authority
- JP
- Japan
- Prior art keywords
- septic tank
- control agent
- pest control
- flies
- formula
- 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.)
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Abstract
(57)【要約】 (修正有)
【課題】 浄化槽内の害虫、コバエ類の防除において、
長期間にわたって効力を持続し得る有効な浄化槽用害虫
防除剤を提供する。
【解決手段】 有効成分として一般式(1)で示される
エステル化合物が、有機高分子化合物に保持されてなる
浄化槽用害虫防除剤。
(式中、Rはメチル基またはメトキシメチル基を表
す。)(57) [Abstract] (Modified) [Problem] In controlling pests and flies in septic tanks,
Provided is an effective pest control agent for a septic tank that can maintain its efficacy for a long period of time. SOLUTION: An insect-controlling agent for a septic tank, wherein an ester compound represented by the general formula (1) is held as an active ingredient by an organic polymer compound. (In the formula, R represents a methyl group or a methoxymethyl group.)
Description
【0001】[0001]
【発明の属する技術分野】本発明は、浄化槽に発生する
害虫の防除及びコバエ類の防除に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to the control of pests generated in a septic tank and the control of flies.
【0002】[0002]
【従来の技術】特開平9−12405号公報において、
有効成分が水溶性固体担体に保持されてなる浄化槽用害
虫駆除剤が知られている。2. Description of the Related Art In Japanese Patent Application Laid-Open No. Hei 9-12405,
BACKGROUND ART Pest control agents for septic tanks in which an active ingredient is held on a water-soluble solid carrier are known.
【0003】[0003]
【発明が解決しようとする課題】しかしながら、該浄化
槽用害虫駆除剤は長期間の効力持続性において必ずしも
十分ではない。本発明は、チョウバエ類、ノミバエ類等
のコバエ類に代表される浄化槽に発生する害虫の有効な
防除、特に長期間にわたる効果的な防除を提供するもの
である。However, the insecticides for septic tanks are not always sufficient in long-term efficacy. The present invention provides an effective control of pests generated in a septic tank typified by a fly, such as a fly and a fly, and particularly an effective control over a long period of time.
【0004】[0004]
【課題を解決するための手段】本発明によれば、有効成
分としての一般式(1) (式中、Rはメチル基またはメトキシメチル基を表
す。)で示されるエステル化合物が有機高分子化合物に
保持されてなる浄化槽用害虫防除剤が、長期間にわたっ
て効力が持続することから、浄化槽に発生する害虫の防
除において極めて有効であるというものである。According to the present invention, general formula (1) as an active ingredient is used. (In the formula, R represents a methyl group or a methoxymethyl group.) Since the insecticidal agent for a septic tank in which an ester compound represented by the following formula (1) is held by an organic polymer compound has a long-lasting effect, It is extremely effective in controlling generated pests.
【0005】また、本発明は、浄化槽に発生する害虫の
代表例であるチョウバエ類、ノミバエ類等のコバエ類の
防除において、有効成分としての前記一般式(1)で示
されるエステル化合物が有機高分子化合物に保持されて
なるコバエ類防除剤が有効であるというものである。Further, the present invention provides a method for controlling fly flies, such as flies and flies, which are typical examples of pests generated in a septic tank, wherein the ester compound represented by the general formula (1) as an active ingredient is highly organic. It is said that a fly control agent held by a molecular compound is effective.
【0006】[0006]
【発明の実施の形態】以下、本発明につき詳細に説明す
る。前記一般式(1)で示されるエステル化合物(以
下、本化合物と記す。)は特開2000-63329に記載の化合
物であり、例えば以下の方法により製造することができ
る。 式(2) で示されるカルボン酸化合物またはその酸クロリドと一
般式(3) (式中、Rは前記と同じ意味を表す。)で示されるアル
コール化合物とを反応させることにより製造する方法。
該反応は、通常有機溶媒中で、必要に応じて反応助剤の
存在下に行われる。反応時間の範囲は通常5分間〜72
時間であり、反応温度の範囲は通常−80℃から反応に
使用する溶媒の沸点または200℃までの範囲である。
式(2)で示されるカルボン酸化合物またはその酸クロ
リドと一般式(3)で示されるアルコール化合物との使
用モル比は1:1またはそれに近い比率で行うのが好ま
しい。反応助剤としては、トリエチルアミン、4−ジメ
チルアミノピリジン、ジイソプロピルエチルアミン等の
3級アミン、ジシクロヘキシルカルボジイミド、1−エ
チル−3−(3−ジメチルアミノプロピル)カルボジイ
ミドハイドロクロリド、ジエチルアゾジカルボキシラー
トまたはジイソプロピルアゾジカルボキシラートとトリ
フェニルホスフィンとの試剤等があげられる。溶媒とし
ては、トルエン、ヘキサン等の炭化水素類、ジエチルエ
ーテル、テトラヒドロフラン等のエーテル類、ジクロロ
メタン、1,2−ジクロロエタン等のハロゲン化炭化水
素類、ジメチルホルムアミド等のアミド類、アセトン等
のケトン類、ジメチルスルホキシド等の有機硫黄類等及
びこれらの混合物があげられる。反応終了後の反応液は
有機溶媒抽出、濃縮等の通常の後処理操作を行うことに
より本化合物を得ることができる。本化合物はクロマト
グラフィー等の操作により精製することもできる。尚、
式(2)で示されるカルボン酸化合物は、J.Che
m.Soc.1076(1970)に記載の方法に準じ
て製造することができ、一般式(3)で示されるアルコ
ール化合物は、特開昭57−123146号公報または
特開昭56−97251号公報に記載の方法に準じて製
造することができる。DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below in detail. The ester compound represented by the general formula (1) (hereinafter, referred to as the present compound) is a compound described in JP-A-2000-63329, and can be produced, for example, by the following method. Equation (2) And a carboxylic acid compound or an acid chloride thereof represented by the general formula (3): (Wherein, R represents the same meaning as described above).
The reaction is usually performed in an organic solvent, if necessary, in the presence of a reaction aid. The reaction time is usually from 5 minutes to 72 minutes.
The reaction temperature is usually in the range from -80 ° C to the boiling point of the solvent used in the reaction or 200 ° C.
The molar ratio of the carboxylic acid compound represented by the formula (2) or the acid chloride thereof to the alcohol compound represented by the general formula (3) is preferably 1: 1 or a ratio close thereto. Examples of the reaction assistant include tertiary amines such as triethylamine, 4-dimethylaminopyridine and diisopropylethylamine, dicyclohexylcarbodiimide, 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride, diethylazodicarboxylate and diisopropylazodiamine. Examples include reagents of dicarboxylate and triphenylphosphine. As the solvent, hydrocarbons such as toluene and hexane, ethers such as diethyl ether and tetrahydrofuran, halogenated hydrocarbons such as dichloromethane and 1,2-dichloroethane, amides such as dimethylformamide, ketones such as acetone, Organic sulfurs such as dimethylsulfoxide and the like and mixtures thereof. After completion of the reaction, the compound can be obtained by subjecting the reaction solution to a usual post-treatment operation such as extraction with an organic solvent and concentration. The present compound can also be purified by an operation such as chromatography. still,
The carboxylic acid compound represented by the formula (2) is described in J. Am. Che
m. Soc. The alcohol compound represented by the general formula (3) can be produced according to the method described in JP-A-57-123146 or JP-A-56-97251. It can be manufactured according to.
【0007】本化合物には不斉炭素に基づく光学異性体
(R,S)や二重結合に基づく幾何異性体(E,Z)や
シクロプロパン環に基づく幾何異性体(シス,トラン
ス)が存在するが、本化合物には害虫防除活性を有する
すべての光学異性体、幾何異性体およびそれらの混合物
が含まれる。This compound has optical isomers (R, S) based on asymmetric carbon, geometric isomers (E, Z) based on a double bond, and geometric isomers (cis, trans) based on a cyclopropane ring. However, the present compounds include all optical isomers, geometric isomers and mixtures thereof having pest control activity.
【0008】本発明の浄化槽用害虫防除剤及びコバエ類
防除剤は、有効成分である本化合物が有機高分子化合物
に保持されてなるものであるが、さらに、他の殺虫成分
化合物や効力増強剤等を含有してもよく、他の殺虫成分
化合物としては、例えば、1−エチニル−2−メチル−
2−ペンテニル クリサンテマート、3−アリル−2−
メチルシクロペンタ−2−エン−4−オン−1−イル
2,2,3,3−テトラメチルシクロプロパンカルボキ
シラート、2,3,5,6−テトラフルオロベンジル
3−(2,2−ジクロロビニル)−2,2−ジメチルシ
クロプロパンカルボキシラート等が挙げられ、効力増強
剤としては、例えば、ピペロニルブトキシド等が挙げら
れる。本発明の浄化槽用害虫防除剤又はコバエ類防除剤
中、本化合物の含有量は、通常、0.5〜20重量%で
ある。The insect pest control agent for purifying tanks and the fly control agent of the present invention are those in which the present compound, which is an active ingredient, is held by an organic polymer compound. And other insecticidal component compounds, for example, 1-ethynyl-2-methyl-
2-pentenyl chrysanthemate, 3-allyl-2-
Methylcyclopenta-2-en-4-one-1-yl
2,2,3,3-tetramethylcyclopropanecarboxylate, 2,3,5,6-tetrafluorobenzyl
3- (2,2-dichlorovinyl) -2,2-dimethylcyclopropanecarboxylate and the like are mentioned, and as the potency enhancer, for example, piperonyl butoxide and the like are mentioned. The content of the present compound in the pesticidal composition for a septic tank or the insecticide of the present invention is usually 0.5 to 20% by weight.
【0009】本発明において用いられる有機高分子化合
物は水不溶性の合成樹脂または合成ゴムであり、なかで
も熱可塑性樹脂又は熱可塑性ゴムの使用が好ましく、例
えば、ポリエチレン、ポリプロピレン、ポリブテン−1
等のα−オレフィン重合体、これらの共重合体(α−オ
レフィン共重合体)、エチレン−酢酸ビニル共重合体、
エチレン−メチル(メタ)アクリレート共重合体、エチ
レン−エチルアクリレート共重合体、エチレン−酢酸ビ
ニル−メチル(メタ)アクリレート共重合体等のエチレ
ン−不飽和カルボン酸系共重合体、ポリ酢酸ビニル、ポ
リカーボネート、ポリエステル、ポリアミド、ポリスチ
レン、ポリメタクリル酸メチル、これらの混合物などが
使用される。特に、α−オレフィン重合体、α−オレフ
ィン共重合体、エチレン−不飽和カルボン酸系共重合体
等のポリオレフィン重合体の使用が好ましい。The organic polymer compound used in the present invention is a water-insoluble synthetic resin or synthetic rubber. Among them, a thermoplastic resin or a thermoplastic rubber is preferably used. Examples thereof include polyethylene, polypropylene, and polybutene-1.
Α-olefin polymers such as these, copolymers thereof (α-olefin copolymer), ethylene-vinyl acetate copolymer,
Ethylene-unsaturated carboxylic acid-based copolymers such as ethylene-methyl (meth) acrylate copolymer, ethylene-ethyl acrylate copolymer, ethylene-vinyl acetate-methyl (meth) acrylate copolymer, polyvinyl acetate, and polycarbonate , Polyester, polyamide, polystyrene, polymethyl methacrylate, and mixtures thereof. Particularly, use of a polyolefin polymer such as an α-olefin polymer, an α-olefin copolymer, and an ethylene-unsaturated carboxylic acid copolymer is preferred.
【0010】本化合物が有機高分子化合物に保持されて
なる本発明の浄化槽用害虫防除剤及びコバエ類防除剤に
は、必要により安定性を付与するために、酸化防止剤、
紫外線吸収剤、抗ブロッキング剤等が加えられる。[0010] The pest control agent for septic tanks and the flies control agent of the present invention, in which the present compound is held by an organic polymer compound, may have an antioxidant, if necessary, in order to impart stability.
UV absorbers, anti-blocking agents and the like are added.
【0011】酸化防止剤としては、例えば、ブチルヒド
ロキシアニソール(BHA)、ステアリル β−(3,
5−ジ−t−ブチル−4−ヒドロキシフェニル)プロピ
オネート、4,4′−チオビス(3−メチル−6−t−
ブチルフェノール)(TBMTBP)、トリフェニルホ
スファイト等が挙げられ、紫外線吸収剤としては、例え
ば、サリチル酸フェニル、2,4−ジヒドロキシベンゾ
フェノン、2−ヒドロキシ−4−メトキシベンゾフェノ
ン、2−(2′−ヒドロキシ−5′−メチルフェニル)
ベンゾトリアゾール等が挙げられ、抗ブロッキング剤と
しては、例えば、澱粉、ワックス、ホウ酸トリブチル等
が挙げられる。Examples of the antioxidant include butylhydroxyanisole (BHA), stearyl β- (3,
5-di-t-butyl-4-hydroxyphenyl) propionate, 4,4'-thiobis (3-methyl-6-t-
Butylphenol) (TBMTBP), triphenyl phosphite, and the like. Examples of the ultraviolet absorber include phenyl salicylate, 2,4-dihydroxybenzophenone, 2-hydroxy-4-methoxybenzophenone, and 2- (2′-hydroxy-). 5'-methylphenyl)
Examples include benzotriazole, and examples of the antiblocking agent include starch, wax, tributyl borate, and the like.
【0012】本化合物が有機高分子化合物に保持されて
なる本発明の浄化槽用害虫防除剤及びコバエ類防除剤
は、有機高分子化合物に本化合物を含浸、塗布等の方法
により保持させたり、単軸押出機、二軸押出機、バンバ
リーミキサー等の混練機を用いて有機高分子化合物と本
化合物とを混練し、適宜成形するなどして製造される。
尚、成形加工時の温度は170℃以下とするのが、成形
時における本化合物の損失を抑制する上で好ましい。The pest control agent for purifying a septic tank and the fly control agent of the present invention in which the present compound is held by an organic polymer compound, the organic polymer compound is impregnated with the compound by a method such as impregnation, coating, etc. It is manufactured by kneading an organic polymer compound and the present compound using a kneader such as a screw extruder, a twin screw extruder, and a Banbury mixer, and appropriately molding.
The temperature at the time of molding is preferably 170 ° C. or less from the viewpoint of suppressing the loss of the present compound at the time of molding.
【0013】本発明の浄化槽用害虫防除剤及びコバエ類
防除剤は、通常、そのまま施用場所に設置され使用され
る。浄化槽内に施用する場合、浄化槽上部から吊るして
使用するのが便利であり、そのために、予めシート状、
紐状、網状等の成形体とするのが好ましい。これらの成
形体は、0.5 〜5mm程度の範囲内の厚さとするのが効力
の持続性等の点から好ましい。使用量は、通常、浄化槽
等の空間1m3当り本化合物量にして0.1〜30g程
度である。尚、本化合物の蒸散効率を高めるために比表
面積(単位体積当りの表面積)の高い形状とすることも
できる。The pest control agent and the fly control agent for septic tanks of the present invention are usually installed and used at the application site as they are. When applied in a septic tank, it is convenient to use it by hanging it from the top of the septic tank.
It is preferable to use a formed body such as a string or a net. It is preferable that these molded articles have a thickness in the range of about 0.5 to 5 mm from the viewpoint of the durability of the effect and the like. The amount is usually about 0.1~30g in the space 1 m 3 per the amount of compound septic tank or the like. Incidentally, in order to increase the evaporation efficiency of the present compound, it may be formed into a shape having a high specific surface area (surface area per unit volume).
【0014】本発明の浄化槽用害虫防除剤は浄化槽内に
発生するチョウバエ類、ノミバエ類、カバエ類、ニセケ
バエ類、ユスリカ類、イエバエ類、ヤブカ類等の害虫防
除に有効である。The pest control agent for septic tanks of the present invention is effective for controlling insect pests such as flies, flies, flies, flies, midges, house flies and falcons which are generated in the septic tank.
【0015】また、本発明のコバエ類防除剤は、浄化槽
内に発生するコバエ類、例えばオオチョウバエ、ホシチ
ョウバエ等のチョウバエ類、オオキモンノミバエ、コア
シキノミバエ、オオアカノミバエ等のノミバエ類、カバ
エ類、ニセケバエ類などのコバエ類の防除に有効であ
る。さらに、ごみため、便所等に発生するショウジョウ
バエ類、トゲハネバエ類、ハヤトビバエ類などのコバエ
類の防除にも有効であり、これらの場所に設置され使用
される。The fly control agent of the present invention is also useful for the flies which are generated in the septic tank, for example, the flies such as Drosophila and Drosophila, the flies such as D. melanogaster, the flies and the flies and the flies. It is effective for controlling flies, such as flies. Furthermore, it is also effective in controlling flies, such as Drosophila, Barnyard fly, and Fly fly, which are generated in toilets due to garbage, and is installed and used in these places.
【0016】[0016]
【実施例】以下、実施例にて本発明をより詳細に説明す
る。 実施例1 (1)エチレン−メチルメタアクリレート共重合体(住友
化学工業株式会社製、商品名:アクリフトWH202)
95重量部と(1R,3R)−2,2−ジメチル−3−
(1−プロペニル)シクロプロパンカルボン酸(2,
3,5,6−テトラフルオロ−4−メチルフェニル)メ
チル 5重量部とを密閉式加圧ニーダー(森山製作所
製)で剪断発熱を利用して溶融混練した後、押出機を用
いて押出しながらホットカットを行いペレットを得た。 (2)次いで、得られたペレットを押出成形機で成形し、
圧さ2mm、幅75cmのシートを製造した。尚、押出
温度はTダイ部において150℃となるように調節し
た。製造されたシートは長さ150cmに切断し、後述
の試験に供する。The present invention will be described below in more detail with reference to examples. Example 1 (1) Ethylene-methyl methacrylate copolymer (manufactured by Sumitomo Chemical Co., Ltd., trade name: Acryft WH202)
95 parts by weight and (1R, 3R) -2,2-dimethyl-3-
(1-propenyl) cyclopropanecarboxylic acid (2,
After melt-kneading 5 parts by weight of 3,5,6-tetrafluoro-4-methylphenyl) methyl in a closed pressure kneader (manufactured by Moriyama Seisakusho) utilizing the heat generated by shearing, hot extruding using an extruder. Cutting was performed to obtain pellets. (2) Then, the obtained pellets are molded by an extrusion molding machine,
A sheet having a pressure of 2 mm and a width of 75 cm was produced. The extrusion temperature was adjusted to 150 ° C. at the T-die. The manufactured sheet is cut into a length of 150 cm and subjected to a test described later.
【0017】実施例2 (1R,3R)−2,2−ジメチル−3−(1−プロペ
ニル)シクロプロパンカルボン酸(2,3,5,6−テ
トラフルオロ−4−メチルフェニル)メチルに代えて
(1R,3R)−2,2−ジメチル−3−(1−プロペ
ニル)シクロプロパンカルボン酸[2,3,5,6−テ
トラフルオロ−4−(メトキシメチル)フェニル]メチ
ルを用いる以外は実施例1と同様にしてシートを得た。Example 2 (1R, 3R) -2,2-Dimethyl-3- (1-propenyl) cyclopropanecarboxylate (2,3,5,6-tetrafluoro-4-methylphenyl) methyl Examples except for using [2,3,5,6-tetrafluoro-4- (methoxymethyl) phenyl] methyl (1R, 3R) -2,2-dimethyl-3- (1-propenyl) cyclopropanecarboxylate A sheet was obtained in the same manner as in Example 1.
【0018】実施例3 実施例1(1)と同一条件にてペレットを作製し、該ペレ
ットを押出機を用いネット成形用異形ダイスを介して押
出すことにより、ストランド径1mm、網目間隔5mm
角の網状成形体を得た。得られた網状成形体を後述の試
験に供する。Example 3 Pellets were prepared under the same conditions as in Example 1 (1), and the pellets were extruded through a deformed die for forming a net using an extruder to obtain a strand diameter of 1 mm and a mesh interval of 5 mm.
A corner net-like molded product was obtained. The obtained reticulated body is subjected to the test described below.
【0019】実施例4 (1R,3R)−2,2−ジメチル−3−(1−プロペ
ニル)シクロプロパンカルボン酸(2,3,5,6−テ
トラフルオロ−4−メチルフェニル)メチルに代えて
(1R,3R)−2,2−ジメチル−3−(1−プロペ
ニル)シクロプロパンカルボン酸[2,3,5,6−テ
トラフルオロ−4−(メトキシメチル)フェニル]メチ
ルを用いる以外は実施例3と同様にして、ストランド径
1mm、網目間隔5mm角の網状成形体を得た。Example 4 (1R, 3R) -2,2-Dimethyl-3- (1-propenyl) cyclopropanecarboxylate (2,3,5,6-tetrafluoro-4-methylphenyl) methyl Examples except for using [2,3,5,6-tetrafluoro-4- (methoxymethyl) phenyl] methyl (1R, 3R) -2,2-dimethyl-3- (1-propenyl) cyclopropanecarboxylate In the same manner as in Example 3, a net-shaped molded product having a strand diameter of 1 mm and a mesh interval of 5 mm square was obtained.
【0020】実施例5 実施例1及び3で得られた成形体試料を開放系の25℃
に設定された部屋に保存し、10日後、30日後、60日後、
90日後、135日後及び180日後に、容積0.34m3のチャン
バー内中央部に吊下げ、密閉したチャンバー内にオオチ
ョウバエ10匹を放す。1日後にオオチョウバエの生死を
観察して死虫率(%)を求める。その結果、実施例1及
び3で得られる試料共に、10日〜 180日保存後の全ての
試料について100%の死虫率が得られる。Example 5 The molded body samples obtained in Examples 1 and 3 were subjected to an open system at 25 ° C.
Saved in the room set in 10 days, 30 days, 60 days,
After 90 days, 135 days and 180 days, the plants are hung in the center of a chamber having a volume of 0.34 m 3 , and ten Drosophila are released into the sealed chamber. One day later, the life and death of Drosophila melanogaster is observed to determine the mortality (%). As a result, both the samples obtained in Examples 1 and 3 achieve 100% mortality for all the samples after storage for 10 to 180 days.
【0021】実施例6 実施例3で得られた成形体試料(本化合物1gを含有)
を浄化槽(2m3)内に設置することにより、浄化槽内
のオオチョウバエ及びオオキモンノミバエを防除するこ
とができる。Example 6 A sample of the molded article obtained in Example 3 (containing 1 g of the present compound)
By installing in a septic tank (2 m 3 ), it is possible to control Drosophila melanogaster and Oleum fleas in the septic tank.
【0022】[0022]
【発明の効果】本発明の浄化槽用害虫防除剤及びコバエ
類防除剤は長期間にわたって効力が持続することから、
浄化槽内の害虫、コバエ類の防除に極めて有効である。EFFECT OF THE INVENTION Since the pesticidal agent for purifying a septic tank and the insecticide for controlling flies of the present invention are effective for a long period of time,
It is extremely effective for controlling pests and flies in septic tanks.
───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 4H011 AC02 BA01 BB15 BC19 DA07 DA10 DC05 DD07 DH02 DH14 DH19 4J002 AA001 AA011 AC001 BB001 EH116 FD186 GC00 ──────────────────────────────────────────────────続 き Continued on the front page F term (reference) 4H011 AC02 BA01 BB15 BC19 DA07 DA10 DC05 DD07 DH02 DH14 DH19 4J002 AA001 AA011 AC001 BB001 EH116 FD186 GC00
Claims (7)
す。)で示されるエステル化合物が、有機高分子化合物
に保持されてなる浄化槽用害虫防除剤。1. A compound represented by the general formula (1) as an active ingredient: (In the formula, R represents a methyl group or a methoxymethyl group.) A pest control agent for a septic tank comprising an ester compound represented by the following formula:
塑性ゴムである請求項1に記載の浄化槽用害虫防除剤。2. The insect pest control agent for a septic tank according to claim 1, wherein the organic polymer compound is a thermoplastic resin or a thermoplastic rubber.
である請求項1に記載の浄化槽用害虫防除剤。3. The pest control agent for a septic tank according to claim 1, wherein the organic high molecular compound is a polyolefin polymer.
す。)で示されるエステル化合物が有機高分子化合物に
保持されてなるコバエ類防除剤。4. The general formula (1) as an active ingredient (In the formula, R represents a methyl group or a methoxymethyl group.) A flies control agent comprising an ester compound represented by the following formula: embedded image
求項4に記載の浄化槽用害虫防除剤。5. The pest control agent for a septic tank according to claim 4, wherein the organic polymer compound is a thermoplastic resin.
である請求項4に記載の浄化槽用害虫防除剤。6. The pest control agent for a septic tank according to claim 4, wherein the organic polymer compound is a polyolefin polymer.
す。)で示されるエステル化合物が、有機高分子化合物
に保持されてなる害虫防除剤を施用することを特徴とす
る浄化槽内の害虫を防除する方法。7. The general formula (1) as an active ingredient (Wherein, R represents a methyl group or a methoxymethyl group). An ester compound represented by the formula (1) is applied with a pest control agent held by an organic polymer compound to control pests in a septic tank. Method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000307405A JP2002114613A (en) | 2000-10-06 | 2000-10-06 | Pest control agent for septic tank |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000307405A JP2002114613A (en) | 2000-10-06 | 2000-10-06 | Pest control agent for septic tank |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2002114613A true JP2002114613A (en) | 2002-04-16 |
Family
ID=18787928
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000307405A Pending JP2002114613A (en) | 2000-10-06 | 2000-10-06 | Pest control agent for septic tank |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2002114613A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002167355A (en) * | 2000-11-29 | 2002-06-11 | Sumitomo Chem Co Ltd | Method for producing ester compound |
| JP2006327938A (en) * | 2005-05-23 | 2006-12-07 | Sumitomo Chemical Co Ltd | How to store pest control agents |
| JP2006348014A (en) * | 2004-09-09 | 2006-12-28 | Sumitomo Chemical Co Ltd | Pest control agent |
| JP2007077068A (en) * | 2005-09-14 | 2007-03-29 | Sumitomo Chemical Co Ltd | How to store pest control agents |
| JP2007077069A (en) * | 2005-09-14 | 2007-03-29 | Sumitomo Chemical Co Ltd | Molded article for pest control |
| JP2007131574A (en) * | 2005-11-10 | 2007-05-31 | Sumika Enviro-Science Co Ltd | Pest control agent |
| KR20200075203A (en) * | 2018-12-17 | 2020-06-26 | 가톨릭대학교 산학협력단 | The method for manufacturing the master batch including insect-proof active ingredient |
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|---|---|---|---|---|
| JPH03200704A (en) * | 1989-12-28 | 1991-09-02 | Sumitomo Chem Co Ltd | Medicine sustained release resin form |
| JPH04120002A (en) * | 1990-09-10 | 1992-04-21 | Earth Chem Corp Ltd | Method for controlling insect pest in purifying facility |
| JPH0912405A (en) * | 1995-04-26 | 1997-01-14 | Fumakilla Ltd | Pest control agent for septic tank and pest control method |
| JPH11171706A (en) * | 1997-12-11 | 1999-06-29 | Sumitomo Chem Co Ltd | Pest control sheet for septic tank |
| JP2000063329A (en) * | 1998-02-26 | 2000-02-29 | Sumitomo Chem Co Ltd | Ester compound |
-
2000
- 2000-10-06 JP JP2000307405A patent/JP2002114613A/en active Pending
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH03200704A (en) * | 1989-12-28 | 1991-09-02 | Sumitomo Chem Co Ltd | Medicine sustained release resin form |
| JPH04120002A (en) * | 1990-09-10 | 1992-04-21 | Earth Chem Corp Ltd | Method for controlling insect pest in purifying facility |
| JPH0912405A (en) * | 1995-04-26 | 1997-01-14 | Fumakilla Ltd | Pest control agent for septic tank and pest control method |
| JPH11171706A (en) * | 1997-12-11 | 1999-06-29 | Sumitomo Chem Co Ltd | Pest control sheet for septic tank |
| JP2000063329A (en) * | 1998-02-26 | 2000-02-29 | Sumitomo Chem Co Ltd | Ester compound |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002167355A (en) * | 2000-11-29 | 2002-06-11 | Sumitomo Chem Co Ltd | Method for producing ester compound |
| JP2006348014A (en) * | 2004-09-09 | 2006-12-28 | Sumitomo Chemical Co Ltd | Pest control agent |
| JP2006327938A (en) * | 2005-05-23 | 2006-12-07 | Sumitomo Chemical Co Ltd | How to store pest control agents |
| JP2007077068A (en) * | 2005-09-14 | 2007-03-29 | Sumitomo Chemical Co Ltd | How to store pest control agents |
| JP2007077069A (en) * | 2005-09-14 | 2007-03-29 | Sumitomo Chemical Co Ltd | Molded article for pest control |
| JP2007131574A (en) * | 2005-11-10 | 2007-05-31 | Sumika Enviro-Science Co Ltd | Pest control agent |
| KR20200075203A (en) * | 2018-12-17 | 2020-06-26 | 가톨릭대학교 산학협력단 | The method for manufacturing the master batch including insect-proof active ingredient |
| KR102161462B1 (en) * | 2018-12-17 | 2020-10-06 | 가톨릭대학교 산학협력단 | The method for manufacturing the master batch including insect-proof active ingredient |
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