JPH09227309A - Termite control agent - Google Patents
Termite control agentInfo
- Publication number
- JPH09227309A JPH09227309A JP3053896A JP3053896A JPH09227309A JP H09227309 A JPH09227309 A JP H09227309A JP 3053896 A JP3053896 A JP 3053896A JP 3053896 A JP3053896 A JP 3053896A JP H09227309 A JPH09227309 A JP H09227309A
- Authority
- JP
- Japan
- Prior art keywords
- control agent
- termite
- termite control
- present
- ethoxymethyl
- 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.)
- Granted
Links
- 241000256602 Isoptera Species 0.000 title claims abstract description 28
- CWFOCCVIPCEQCK-UHFFFAOYSA-N chlorfenapyr Chemical compound BrC1=C(C(F)(F)F)N(COCC)C(C=2C=CC(Cl)=CC=2)=C1C#N CWFOCCVIPCEQCK-UHFFFAOYSA-N 0.000 claims abstract description 11
- 230000000694 effects Effects 0.000 abstract description 8
- 239000004480 active ingredient Substances 0.000 abstract description 2
- 239000003795 chemical substances by application Substances 0.000 description 13
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 241000238631 Hexapoda Species 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000002023 wood Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 description 3
- ZNOLGFHPUIJIMJ-UHFFFAOYSA-N fenitrothion Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C(C)=C1 ZNOLGFHPUIJIMJ-UHFFFAOYSA-N 0.000 description 3
- 239000003350 kerosene Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- 231100000419 toxicity Toxicity 0.000 description 3
- 230000001988 toxicity Effects 0.000 description 3
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
- PCYWMDGJYQAMCR-UHFFFAOYSA-N 1h-pyrrole-3-carbonitrile Chemical compound N#CC=1C=CNC=1 PCYWMDGJYQAMCR-UHFFFAOYSA-N 0.000 description 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
- 239000005944 Chlorpyrifos Substances 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
- SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- 239000003992 organochlorine insecticide Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 241000978776 Senegalia senegal Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 235000012216 bentonite Nutrition 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- BIWJNBZANLAXMG-YQELWRJZSA-N chloordaan Chemical compound ClC1=C(Cl)[C@@]2(Cl)C3CC(Cl)C(Cl)C3[C@]1(Cl)C2(Cl)Cl BIWJNBZANLAXMG-YQELWRJZSA-N 0.000 description 1
- HRBKVYFZANMGRE-UHFFFAOYSA-N chlorpyrifos-methyl Chemical compound COP(=S)(OC)OC1=NC(Cl)=C(Cl)C=C1Cl HRBKVYFZANMGRE-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- DFBKLUNHFCTMDC-PICURKEMSA-N dieldrin Chemical compound C([C@H]1[C@H]2[C@@]3(Cl)C(Cl)=C([C@]([C@H]22)(Cl)C3(Cl)Cl)Cl)[C@H]2[C@@H]2[C@H]1O2 DFBKLUNHFCTMDC-PICURKEMSA-N 0.000 description 1
- 229950006824 dieldrin Drugs 0.000 description 1
- NGPMUTDCEIKKFM-UHFFFAOYSA-N dieldrin Natural products CC1=C(Cl)C2(Cl)C3C4CC(C5OC45)C3C1(Cl)C2(Cl)Cl NGPMUTDCEIKKFM-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- -1 etc.) Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- ATROHALUCMTWTB-OWBHPGMISA-N phoxim Chemical compound CCOP(=S)(OCC)O\N=C(\C#N)C1=CC=CC=C1 ATROHALUCMTWTB-OWBHPGMISA-N 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 150000005846 sugar alcohols Chemical class 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
(57)【要約】
【課題】 低薬量でシロアリの駆除効果を示すシロアリ
防除剤の提供。
【解決手段】 4−ブロモ−2−(4−クロロフェニ
ル)−1−(エトキシメチル)−5−(トリフルオロメ
チル)ピロール−3−カルボニトリルを有効成分とする
シロアリ防除剤。(57) [Abstract] [PROBLEMS] To provide a termite controlling agent showing a termite exterminating effect at a low dose. A termite control agent containing 4-bromo-2- (4-chlorophenyl) -1- (ethoxymethyl) -5- (trifluoromethyl) pyrrole-3-carbonitrile as an active ingredient.
Description
【0001】[0001]
【発明の属する技術分野】本発明は、4−ブロモ−2−
(4−クロロフェニル)−1−(エトキシメチル)−5
−(トリフルオロメチル)ピロール−3−カルボニトリ
ルを含有することを特徴とするシロアリ防除剤に関す
る。TECHNICAL FIELD The present invention relates to 4-bromo-2-
(4-chlorophenyl) -1- (ethoxymethyl) -5
The present invention relates to a termite control agent containing-(trifluoromethyl) pyrrole-3-carbonitrile.
【0002】[0002]
【従来の技術】シロアリは建築物や樹木等を食害し、木
材の他にもコンクリートやビニール製品等をも加害する
ために、薬剤による防除、駆除が必要とされている。従
来、シロアリ防除剤としてクロルデン、ディルドリンな
どの有機塩素系殺虫剤やフェニトロチオン、ホキシム、
クロルピリホスなどの有機リン系殺虫剤が用いられてき
た。しかしながら、有機塩素系殺虫剤は、毒性、残留毒
性、環境汚染などの問題があり使用が禁止され、有機リ
ン系殺虫剤についても、毒性、安定性、残効性などの点
で問題が多く新規なシロアリ防除剤の開発が求められて
いた。2. Description of the Related Art Termites are harmful to buildings and trees, and to concrete as well as wood products as well as wood. Conventionally, as a termite control agent, chlordane, organochlorine insecticides such as dieldrin and fenitrothion, phoxime,
Organic phosphorus insecticides such as chlorpyrifos have been used. However, organochlorine insecticides are prohibited from use due to problems such as toxicity, residual toxicity, and environmental pollution.Organophosphorus insecticides also have many problems in terms of toxicity, stability, residual effect, etc. There has been a demand for the development of new termite control agents.
【0003】また、4−ブロモ−2−(4−クロロフェ
ニル)−1−(エトキシメチル)−5−(トリフルオロ
メチル)ピロール−3−カルボニトリル(特開平1−1
04042号公報)は、殺ダニ剤として知られている
が、シロアリについては開示されていない。Further, 4-bromo-2- (4-chlorophenyl) -1- (ethoxymethyl) -5- (trifluoromethyl) pyrrole-3-carbonitrile (Japanese Patent Application Laid-Open No. 1-111)
No. 04042) is known as an acaricide, but is not disclosed for termites.
【0004】[0004]
【発明が解決しようとする課題】本発明は、従来シロア
リ剤が有していた問題点を解決し、安全性、安定性、防
蟻効果、残効性に優れたシロアリ防除剤を提供しようと
するものである。DISCLOSURE OF THE INVENTION The present invention intends to solve the problems of conventional termite agents and to provide a termite control agent which is excellent in safety, stability, termite control effect and residual effect. To do.
【0005】[0005]
【課題を解決するための手段】本発明者らは、上記課題
を解決するために鋭意研究を重ねた結果、4−ブロモ−
2−(4−クロロフェニル)−1−(エトキシメチル)
−5−(トリフルオロメチル)ピロール−3−カルボニ
トリルが低毒性で且つ低薬量でシロアリに対して高い活
性を示すことを見い出し本発明を完成するに至った。Means for Solving the Problems As a result of intensive studies to solve the above problems, the present inventors have found that 4-bromo-
2- (4-chlorophenyl) -1- (ethoxymethyl)
The inventors have found that -5- (trifluoromethyl) pyrrole-3-carbonitrile has low toxicity and high activity against termites at a low dose, and thus completed the present invention.
【0006】即ち、本発明の要旨は、4−ブロモ−2−
(4−クロロフェニル)−1−(エトキシメチル)−5
−(トリフルオロメチル)ピロール−3−カルボニトリ
ルを含有することを特徴とするシロアリ防除剤に存す
る。That is, the gist of the present invention is 4-bromo-2-
(4-chlorophenyl) -1- (ethoxymethyl) -5
A termite control agent is characterized by containing-(trifluoromethyl) pyrrole-3-carbonitrile.
【0007】[0007]
【発明の実施の形態】以下、本発明を詳細に説明する。
本発明のシロアリ防除剤は、〔以下、クロルフェナピル
と記す。クロルフェナピルは4−ブロモ−2−(4−ク
ロロフェニル)−1−(エトキシメチル)−5−(トリ
フルオロメチル)ピロール−3−カルボニトリルの一般
名である。〕を製剤中0.1〜90重量%含有する。BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be described in detail below.
The termite control agent of the present invention [hereinafter, referred to as chlorfenapyr. Chlorphenapyr is the generic name for 4-bromo-2- (4-chlorophenyl) -1- (ethoxymethyl) -5- (trifluoromethyl) pyrrole-3-carbonitrile. ] In an amount of 0.1 to 90% by weight.
【0008】本発明のシロアリ防除剤の剤型としては、
防除剤の性状、使用目的などにより、油剤、乳剤、水和
剤、水溶剤、粉剤、エアゾール剤など種々可能である
が、油剤、乳剤が一般的に使用される。いずれの製剤も
常法にしたがって調製することができる。固体坦体とし
ては粘土類(例えばカオリン、ベントナイト類、酸性白
土など)、タルク類(例えばタルクなど)、シリカ類
(例えばけい藻土、けい砂、雲母、合成けい酸塩、合成
高分散けい酸など)、パイロフィライト、軽石、砂など
の無機鉱物性粉末等を挙げることができる。これらは単
独で使用してもまたは2種以上の混合物の形で使用して
もよい。The dosage form of the termite controlling agent of the present invention is as follows:
Various agents such as oils, emulsions, wettable powders, water solutions, powders and aerosols can be used depending on the properties of the control agent and the purpose of use, but oils and emulsions are generally used. Any formulation can be prepared according to a conventional method. Solid carriers include clays (eg kaolin, bentonites, acid clay, etc.), talc (eg talc, etc.), silicas (eg diatomaceous earth, silica sand, mica, synthetic silicates, synthetic highly dispersed silica). Etc.), pyrophyllite, pumice stone, inorganic mineral powder such as sand, and the like. These may be used alone or in the form of a mixture of two or more kinds.
【0009】液体坦体としては、水、アルコール類(例
えばメチルアルコール、エチルアルコール、エチレング
リコールなど)、ケトン類(例えばアセトン、メチルエ
チルケトン、シクロヘキサン)、エーテル類(例えばエ
チルエーテル、ジオキサン、テトラハイドロフラン、セ
ルソルブなど)、芳香族炭化水素類(例えばトルエン、
キシレン、ベンゼン、ソルベントナフサ、シクロヘキサ
ン、メチルナフタレンなど)、脂肪族炭化水素類(例え
ばケロシン、灯油など)、エステル類、ニトリル類など
が使用できるが、これらは単独で使用してもまたは2種
以上の混合物の形で使用してもよい。As the liquid carrier, water, alcohols (eg methyl alcohol, ethyl alcohol, ethylene glycol etc.), ketones (eg acetone, methyl ethyl ketone, cyclohexane), ethers (eg ethyl ether, dioxane, tetrahydrofuran), Cersolve, etc.), aromatic hydrocarbons (eg toluene,
Xylene, benzene, solvent naphtha, cyclohexane, methylnaphthalene, etc.), aliphatic hydrocarbons (eg kerosene, kerosene, etc.), esters, nitriles, etc. can be used, but these can be used alone or in combination of two or more. You may use it in the form of the mixture of.
【0010】次に界面活性剤としては、アルキル硫酸エ
ステル類、アルキルアリールスルホン酸塩、ポリエチレ
ングリコールエーテル類、多価アルコールエステル類な
どが挙げられるが、これらに限定されるものではなく、
また、これらを単独で使用してもまたは2種以上の混合
物の形で使用してもよい。その他適宜、カゼイン、ゼラ
チン、澱粉粉、アルギン酸、CMC(カルボキシメチル
セルロース)、アラビアゴム、寒天、ポリビニルアルコ
ールなどの固着剤や分散剤が使用されるが、これらに限
定されるものではない。Next, examples of the surfactant include, but are not limited to, alkyl sulfates, alkylaryl sulfonates, polyethylene glycol ethers, and polyhydric alcohol esters.
These may be used alone or in the form of a mixture of two or more kinds. Other suitable adhesives and dispersants such as casein, gelatin, starch, alginic acid, CMC (carboxymethyl cellulose), gum arabic, agar, and polyvinyl alcohol are used, but the present invention is not limited thereto.
【0011】本発明のシロアリ防除剤は、土壌またはシ
ロアリの生息部位に処理されるほか、シロアリから樹
木、塀、杭、枕木等の木質物体、社寺、家屋、納屋、工
場等の建築物等を保護するためにこれらの周辺または床
下の土壌表面もしくはこれらの周辺または床下の土中に
処理されるのみならず、合板、製材品、パーティクルボ
ード、ハーフボード等の木質製品や被覆電線、シート等
のビニール製品等に使用することもできる。また、あら
かじめシロアリの発生が予測される箇所等に予防的に処
理する態様も本発明に包含されるものである。The termite control agent of the present invention is applied to the soil or the habitat of termites, and also removes wood materials such as trees, fences, piles, sleepers, buildings such as shrines, houses, barns and factories from termites. In order to protect it, it is not only treated on the soil surface under these or under the floor or on the soil around these or under the floor, but also wood products such as plywood, lumber products, particle boards, half boards, coated electric wires, sheets, etc. It can also be used for vinyl products. Further, the present invention also includes a mode in which prophylactic treatment is applied to a place where the occurrence of termites is predicted in advance.
【0012】[0012]
【実施例】次に、実施例及び試験例を示して、本発明の
効果について具体的に説明するが、本発明はその要旨を
越えない限り、以下の実施例に限定されるものではな
い。 〈実施例1〉クロルフェナピル0.3部を灯油に溶解し
て全体を100部としてシロアリ防除剤の油剤を得た。 〈実施例2〉 クロルフェナピル5部、ニューカルゲン
1070(界面活性剤、竹本油脂社製、商標)5部、キ
シレン90部を加え、これらをよく攪拌混合溶解してシ
ロアリ防除剤の乳剤を得た。 〈試験例1〉所定濃度に調整したクロルフェナピルのア
セトン溶液を、マイクロシリンジを用いてイエシロアリ
職蟻の虫体に滴下した。その後、水を含ませた濾紙を与
え、25℃の恒温室に保管し、24時間後の死亡虫数お
よび濾紙の食害度を対照薬剤と比較した。供試虫数は各
濃度段階あたり30個体とした。結果を表1に示す。対
照薬剤として、フェニトロチオン〔O,O−ジメチル−
O−(3−メチル−4−ニトロフェニル)チオホスフェ
ートの一般名〕およびクロルピリホス(O,O−ジメチ
ル−O−3,5,6−トリクロル−2−ピリジルホスホ
ロチオエートの一般名)を使用した。また、表中の食害
度は、−:食害なし、+:軽度な食害、++:ろ紙の周
辺をかなり食害、+++:全面にわたり激しく食害を表
す。EXAMPLES Next, the effects of the present invention will be specifically described by showing Examples and Test Examples, but the present invention is not limited to the following Examples unless it exceeds the gist. <Example 1> 0.3 parts of chlorfenapyr was dissolved in kerosene to make 100 parts as a whole to obtain an oil agent for controlling termites. <Example 2> 5 parts of chlorfenapyr, 5 parts of Newcargen 1070 (surfactant, manufactured by Takemoto Yushi-Seiyaku Co., Ltd., trademark) and 90 parts of xylene were added and well mixed by stirring to obtain a termite control agent emulsion. <Test Example 1> An acetone solution of chlorfenapyr adjusted to a predetermined concentration was dropped onto the insect body of the termite worker ant using a microsyringe. Then, a filter paper containing water was given and stored in a thermostatic chamber at 25 ° C., and the number of dead insects after 24 hours and the degree of feeding damage of the filter paper were compared with the control drug. The number of test insects was 30 at each concentration step. The results are shown in Table 1. As a control drug, fenitrothion [O, O-dimethyl-
O- (3-methyl-4-nitrophenyl) thiophosphate (generic name) and chlorpyrifos (generic name of O, O-dimethyl-O-3,5,6-trichloro-2-pyridylphosphorothioate) were used. In addition, the eating damage degree in the table is as follows:-: no eating damage, +: mild eating damage, ++: considerable eating damage around the filter paper, and +++: severe eating damage over the entire surface.
【0013】[0013]
【表1】 [Table 1]
【0014】〈試験例2〉実施例2で得た乳剤を水道水
で200倍に希釈し、ラワン材片(2×2×2cm)表
面にクロルフェナピルの有効成分量として0.25mg
/m2 となるように塗布した。対照薬剤についても実施
例2に準じた方法で調整し、同様の濃度で塗布した。こ
の供試材片と水を含ませた濾紙をイエシロアリ職蟻50
個体に加え、25℃の恒温室に保管し、24時間後、4
8時間後および72時間後の死亡虫数を調査した。結果
を表2に示す。<Test Example 2> The emulsion obtained in Example 2 was diluted 200 times with tap water, and 0.25 mg as an active ingredient amount of chlorfenapyr on the surface of a lauan piece (2 x 2 x 2 cm).
/ M 2 . The control drug was also prepared in the same manner as in Example 2 and applied at the same concentration. Filter paper containing this test piece and water
In addition to the individual, store in a constant temperature room at 25 ° C, and after 24 hours, 4
The number of dead insects was examined after 8 hours and 72 hours. Table 2 shows the results.
【0015】[0015]
【表2】 [Table 2]
【0016】[0016]
【発明の効果】クロルフェナピルをシロアリまたはシロ
アリの生活環境に対して使用することにより、低薬量で
シロアリの駆除に高い活性を示す。EFFECTS OF THE INVENTION By using chlorfenapyr against termites or termite living environments, it exhibits high activity for controlling termites with a low dose.
Claims (2)
ル)−1−(エトキシメチル)−5−(トリフルオロメ
チル)ピロール−3−カルボニトリルを含有することを
特徴とするシロアリ防除剤。1. A termite control agent comprising 4-bromo-2- (4-chlorophenyl) -1- (ethoxymethyl) -5- (trifluoromethyl) pyrrole-3-carbonitrile.
ル)−1−(エトキシメチル)−5−(トリフルオロメ
チル)ピロール−3−カルボニトリルを0.1〜90重
量%含有することを特徴とする請求項1に記載のシロア
リ防除剤。2. Containing 0.1 to 90% by weight of 4-bromo-2- (4-chlorophenyl) -1- (ethoxymethyl) -5- (trifluoromethyl) pyrrole-3-carbonitrile. The termite control agent according to claim 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP03053896A JP3713584B2 (en) | 1996-02-19 | 1996-02-19 | Termite control agent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP03053896A JP3713584B2 (en) | 1996-02-19 | 1996-02-19 | Termite control agent |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH09227309A true JPH09227309A (en) | 1997-09-02 |
| JP3713584B2 JP3713584B2 (en) | 2005-11-09 |
Family
ID=12306583
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP03053896A Expired - Fee Related JP3713584B2 (en) | 1996-02-19 | 1996-02-19 | Termite control agent |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3713584B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0895717A1 (en) * | 1997-08-08 | 1999-02-10 | American Cyanamid Company | Arylpyrroles for subterranean termite control |
| JP2009523685A (en) * | 2005-11-02 | 2009-06-25 | エスイーピー イノヴァテルム | Structural barrier (BSB) with biocides |
-
1996
- 1996-02-19 JP JP03053896A patent/JP3713584B2/en not_active Expired - Fee Related
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0895717A1 (en) * | 1997-08-08 | 1999-02-10 | American Cyanamid Company | Arylpyrroles for subterranean termite control |
| JP2009523685A (en) * | 2005-11-02 | 2009-06-25 | エスイーピー イノヴァテルム | Structural barrier (BSB) with biocides |
Also Published As
| Publication number | Publication date |
|---|---|
| JP3713584B2 (en) | 2005-11-09 |
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