JPH0482805A - Acarid control agent and acarid control material - Google Patents
Acarid control agent and acarid control materialInfo
- Publication number
- JPH0482805A JPH0482805A JP19450390A JP19450390A JPH0482805A JP H0482805 A JPH0482805 A JP H0482805A JP 19450390 A JP19450390 A JP 19450390A JP 19450390 A JP19450390 A JP 19450390A JP H0482805 A JPH0482805 A JP H0482805A
- Authority
- JP
- Japan
- Prior art keywords
- agent
- acarid
- acarid control
- mites
- mite
- 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.)
- Pending
Links
- 239000000463 material Substances 0.000 title claims abstract description 17
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- NFLGAXVYCFJBMK-UHFFFAOYSA-N isomenthone Natural products CC(C)C1CCC(C)CC1=O NFLGAXVYCFJBMK-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000000642 acaricide Substances 0.000 claims description 15
- -1 hydrate Substances 0.000 abstract description 19
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- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract description 7
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- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract description 6
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- 241000238710 Dermatophagoides Species 0.000 description 6
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- 230000000694 effects Effects 0.000 description 6
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- 150000001298 alcohols Chemical class 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
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- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
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- 239000003205 fragrance Substances 0.000 description 2
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- 230000002588 toxic effect Effects 0.000 description 2
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- 239000002023 wood Substances 0.000 description 2
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 1
- NOOLISFMXDJSKH-AEJSXWLSSA-N (+)-menthol Chemical compound CC(C)[C@H]1CC[C@H](C)C[C@@H]1O NOOLISFMXDJSKH-AEJSXWLSSA-N 0.000 description 1
- VEMKTZHHVJILDY-PMACEKPBSA-N (5-benzylfuran-3-yl)methyl (1r,3s)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-PMACEKPBSA-N 0.000 description 1
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
- OVHLWVRXNWBIJE-UHFFFAOYSA-N (cyano-phenoxy-phenylmethyl) 2-(4-chlorophenyl)-3-methylbutanoate Chemical compound C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C=1C=CC=CC=1)(C#N)OC1=CC=CC=C1 OVHLWVRXNWBIJE-UHFFFAOYSA-N 0.000 description 1
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 241000239290 Araneae Species 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- 241000723346 Cinnamomum camphora Species 0.000 description 1
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 1
- 241000238713 Dermatophagoides farinae Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- PNVJTZOFSHSLTO-UHFFFAOYSA-N Fenthion Chemical compound COP(=S)(OC)OC1=CC=C(SC)C(C)=C1 PNVJTZOFSHSLTO-UHFFFAOYSA-N 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
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- ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
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- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
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- DDTBPAQBQHZRDW-UHFFFAOYSA-N cyclododecane Chemical compound C1CCCCCCCCCCC1 DDTBPAQBQHZRDW-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 1
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 1
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- VKLYZBPBDRELST-UHFFFAOYSA-N ethene;methyl 2-methylprop-2-enoate Chemical compound C=C.COC(=O)C(C)=C VKLYZBPBDRELST-UHFFFAOYSA-N 0.000 description 1
- BNKAXGCRDYRABM-UHFFFAOYSA-N ethenyl dihydrogen phosphate Chemical compound OP(O)(=O)OC=C BNKAXGCRDYRABM-UHFFFAOYSA-N 0.000 description 1
- YIWFBNMYFYINAD-UHFFFAOYSA-N ethenylcyclopropane Chemical compound C=CC1CC1 YIWFBNMYFYINAD-UHFFFAOYSA-N 0.000 description 1
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- ZNOLGFHPUIJIMJ-UHFFFAOYSA-N fenitrothion Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C(C)=C1 ZNOLGFHPUIJIMJ-UHFFFAOYSA-N 0.000 description 1
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- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
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- 150000008282 halocarbons Chemical class 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
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- 150000002739 metals Chemical class 0.000 description 1
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- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
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Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【発明の詳細な説明】 〈産業上の利用分野〉 本発明は新規なダニ防除剤及びダニ防除材に関する。[Detailed description of the invention] <Industrial application field> The present invention relates to a novel mite control agent and a new mite control material.
〈従来の技術〉
一般家庭の室内塵中には必ずと言ってよい程ダニが生息
しているが、近年、住宅、生活様式の変化に伴いダニの
多発が見られるようになった。従来よりこのような室内
塵性のダニに対するダニ防除材としては、例えばフェニ
トロチオン、フェンチオン、DDVP、ダイアジノン等
の有機リン系化合物、プロポクサー、NAC等のカーバ
メイト系化合物、レスメトリン等のピレスロイド系の化
合物が知られている。<Prior Art> Dust mites are almost always present in the indoor dust of ordinary households, but in recent years, with changes in housing and lifestyles, the number of mites has increased. Conventionally, as mite control materials against indoor dust mites, organic phosphorus compounds such as fenitrothion, fenthion, DDVP, and diazinon, carbamate compounds such as propoxar and NAC, and pyrethroid compounds such as resmethrin have been known. It is being
〈発明が解決しようとする問題点〉
これら公知のダニ防除剤は、畳、カーペット、シートに
保持させたり、そのまま散布、噴霧等して用いられてい
るが、次のような短所を有している。すなわち、有機リ
ン系のダニ防除剤は、毒性が高く、悪臭を有し、ヒヨウ
ヒダニ類に対する効果が低いという短所を有し、カーバ
メイト系のダニ防除剤は、毒性が高く、ヒヨウヒダニ類
に刻する効果が低いという短所を有し、ピレスロイド系
のダニ防除剤は、高価であり、ケナガコナダニに対する
効果が低いという短所を有している。又これらのダニ防
除剤を絹み合わせて使用する場合使いづらいというよう
な種々の問題点をも含んでいる。<Problems to be Solved by the Invention> These known mite control agents are used by keeping them on tatami mats, carpets, and sheets, or by scattering or spraying them as they are, but they have the following disadvantages. There is. In other words, organophosphorus-based mite control agents have the disadvantages of being highly toxic, have a bad odor, and have low effectiveness against Dermatophagoides mites, while carbamate-based mite control agents are highly toxic and have a low effect on Dermatophagoides mites. However, pyrethroid-based mite control agents have the disadvantages of being expensive and having low effectiveness against woolly mites. Furthermore, there are various problems such as difficulty in using these mite control agents together.
く問題点を解決するための手段〉
そこで本発明者は、毒性が低く、幅広いダニ防除領域を
持つ、安価なダニ防除剤を提供するため種々研究を重ね
た結果、託−メントール及び/又はその異性体が」二記
要件を満たすことを見い出した。Means for Solving the Problems> Therefore, the present inventor has conducted various studies to provide an inexpensive tick control agent that is low in toxicity and has a wide range of tick control areas, and has developed It has been found that the isomer satisfies the requirements described in item 2.
すなわち、d9−メントール及び/又はその異性体を有
効成分として含有することを特徴とするダニ防除剤、及
び該防除剤を基材に保持させたことを特徴とするダニ防
除拐に係る。That is, the present invention relates to a mite-controlling agent characterized by containing d9-menthol and/or its isomer as an active ingredient, and a mite-controlling agent characterized by holding the mite-controlling agent on a base material.
本発明のダニ防除剤は、その有効成分としてdεメント
ール、dL−(±)−メントール、dL−(±)−ネオ
メントール、dL−(±)−イソメントール、dL−(
±)−ネオイソメントール、dg−(−)−メントール
、dg−(−)−ネオメントール、dL−(−)−イソ
メントール、dg−(−)−ネオイソメントール、dg
−(十)メントール、dL−(+)−ネオメントール、
dg−(+)イソメントール、dg−(十)−ネオイソ
メントールより選ばれた少なくとも1種を含有すること
により、極めて優れたダニ防除効果を示す。その対象と
なるダニ類は、いずれの種類でも対象となり得るが、特
にコナヒヨウヒダニやヤケヒヨウヒダニ等のヒヨウヒダ
ニ類、ケナガコナダニやムギコナダニ等のコナダニ類、
チリニクダニやイエニクダニ等のニクダニ類、ホコリダ
ニ類、クワガタツメダニやフトツメダニ等のツメダニ類
、イエダニやトリサシダニ等の動物寄生性ダニ類が挙げ
られる。The mite control agent of the present invention contains dε-menthol, dL-(±)-menthol, dL-(±)-neomenthol, dL-(±)-isomenthol, dL-(
±)-neoisomenthol, dg-(-)-menthol, dg-(-)-neomenthol, dL-(-)-isomenthol, dg-(-)-neoisomenthol, dg
-(10) menthol, dL-(+)-neomenthol,
By containing at least one selected from dg-(+)isomenthol and dg-(10)-neisomenthol, it exhibits an extremely excellent mite control effect. The target mites can be any type of mites, but in particular, the mites such as Dermatophagoides nigricans and Dermatophagoides nigra, the Dermatophagoides mites such as the woolly spider mite and the wheat mite,
Examples include dust mites such as dust mites and house dust mites, dust mites such as stag mites and foot mites, and animal parasitic mites such as house dust mites and staghorn mites.
本発明のダニ防除剤は、上記有効成分を含有する防除剤
をそのまま用いることもできるが、通常は液体担体及び
固体担体にその有効成分を含有する防除剤を保持させ、
必要に応じ塗膜形成剤、乳化剤、分散剤、展着剤、湿潤
剤、安定剤、噴射剤、揮散調整剤等を添加して、油剤、
乳剤、水利剤、噴霧剤、エアゾール剤、燻煙剤、塗布剤
、粉剤、粒剤等の形態で使用することができる。前記液
体担体としては、水や例えばメチルアルコール、エチル
アルコール、イソプロピルアルコール等のアルコール類
、アセトン、メチルエチルケトン、シクロヘキサノン等
のケトン類、テトラヒドロフラン、ジオキサン、ジメチ
ルエーテル等のエーテル類、ヘキサン、ケロシン、ノル
マルパラフィン、ソルベントナフサ等の脂肪族炭化水素
類、ベンゼン、トルエン等の芳香族炭化水素類、ジクロ
ロメタン、ジクロロエタン等のハロゲン化炭化水素類、
酢酸エチル、酢酸ブチル等のエステル類等を挙げること
ができる。固体担体としては、例えばケイ酸、カオリン
、活性炭、ベントナイト、ケイソウ上、タルク、クレー
、炭酸カルシウム、陶磁器粉等の鉱物性粉末、木粉、大
豆粉、小麦粉、でん粉等の植物質粉末、シクロデキスト
リン等の包接化合物等を挙げることができる。For the mite control agent of the present invention, the control agent containing the above-mentioned active ingredient can be used as it is, but usually, the control agent containing the active ingredient is held in a liquid carrier or a solid carrier,
Add film-forming agents, emulsifiers, dispersants, spreading agents, wetting agents, stabilizers, propellants, volatility regulators, etc. as necessary to prepare oils,
It can be used in the form of an emulsion, an aqueous solution, a spray, an aerosol, a smoke, a liniment, a powder, a granule, and the like. Examples of the liquid carrier include water, alcohols such as methyl alcohol, ethyl alcohol, and isopropyl alcohol, ketones such as acetone, methyl ethyl ketone, and cyclohexanone, ethers such as tetrahydrofuran, dioxane, and dimethyl ether, hexane, kerosene, normal paraffin, and solvents. Aliphatic hydrocarbons such as naphtha, aromatic hydrocarbons such as benzene and toluene, halogenated hydrocarbons such as dichloromethane and dichloroethane,
Examples include esters such as ethyl acetate and butyl acetate. Examples of solid carriers include mineral powders such as silicic acid, kaolin, activated carbon, bentonite, diatomaceous powder, talc, clay, calcium carbonate, and ceramic powder, vegetable powders such as wood flour, soy flour, wheat flour, and starch, and cyclodextrin. Examples include clathrate compounds such as.
尚、塗膜形成剤としては、セルロース誘導体、ビニル系
樹脂、アルキッド系樹脂、ユリア系樹脂、エポキシ系樹
脂、ポリエステル系樹脂、ウレタン系樹脂、シリコン系
樹脂、アクリル系樹脂、塩化ゴム、ポリビニルアルコー
ル等を、又乳化剤、分散剤、展着剤としては、石けん類
、ポリオキシエチレンアルキルエーテル、ポリオキシエ
チレンアルキルフェニ一
ルエーテル、ポリオキシエチレン脂肪酸エステル、脂肪
酸グリセリド、ソルビタン脂肪酸エステル、高級アルコ
ールの硫酸エステル、アルキルアリルスルホン酸塩等の
界面活性剤を、さらに噴射剤としては、液化石油ガス、
ジメチルエーテル、CO2、フルオロカーボン等を例示
できる。又、揮散調整剤として、トリシクロデカン、シ
クロドデカン、2. 4.、 6トリイソプロビルー1
.3.5−トリオキサン、トリメチレンノルボルネン等
の昇華性担体やバラジクロロベンゼン、ナフタリン、樟
脳等の昇華性防虫剤を用い、前記ダニ防除剤を昇華性固
剤とすることもできるし、エムペントリン、DDVP等
の揮散性防虫剤を組み合せ、揮散性ダニ防除剤として使
用することもできる。In addition, examples of coating film forming agents include cellulose derivatives, vinyl resins, alkyd resins, urea resins, epoxy resins, polyester resins, urethane resins, silicone resins, acrylic resins, chlorinated rubber, polyvinyl alcohol, etc. In addition, as emulsifiers, dispersants, and spreading agents, soaps, polyoxyethylene alkyl ethers, polyoxyethylene alkyl phenyl ethers, polyoxyethylene fatty acid esters, fatty acid glycerides, sorbitan fatty acid esters, sulfuric esters of higher alcohols, Surfactants such as alkylaryl sulfonates, and propellants such as liquefied petroleum gas,
Examples include dimethyl ether, CO2, and fluorocarbon. Further, as a volatilization regulator, tricyclodecane, cyclododecane, 2. 4. , 6-triisoprobyl-1
.. 3. The mite control agent can be made into a sublimable solid agent by using a sublimable carrier such as 5-trioxane or trimethylene norbornene or a sublimable insect repellent such as balajichlorobenzene, naphthalene, or camphor. It can also be used as a volatile mite control agent in combination with other volatile insect repellents.
さらに本発明のダニ防除剤には、各種の防虫剤、協力剤
、害虫忌避剤、ネズミ忌避剤、酸化防止剤、分解防止剤
、殺菌剤、防黴剤、香料、着色料等を配合することもで
きる。配合可能な防虫剤としては、従来より害虫駆除に
用いられる各種薬剤がいずれも使用できる。代表的薬剤
としては、3−アリル−2−メチルシクロペンタ−2−
エン−4−オン−1イル dl−シス/トランスークリ
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 d−シス/トランスー
クリサンテマート d−3−アリル−2−メチルシクロ
ペンタ−2−エン−4−オン−1−イル d−)ランス
ークリサンテマート、3−アリル−2−メチルシクロペ
ンタ−2−エン−4−オン−1−イル dトランスーク
リサンテマート、N−(3・4・5・6−チトラヒドロ
フタリミド)−メチル dl−シス/トランスークリサ
ンテマート、5−ベンジル3−フリルメチル d−シス
/トランスークリサンテマート、5−(2−プロパギル
)−3−フリルメチルクリサンテマート 3−フェノキ
シベンジル2・2−ジメチル−3−(2’ ・2°−
ジクロロ)ビニルシクロプロパン力ルポキシレート、3
−フェノキシベンジル d−シス/トランスークリサン
テマート、α−シアノフェノキシベンジル イソプロピ
ル−4−クロロフェニルアセテート、 (S)−α−シ
アノ−3−フェノキシベンジル(IR・シス)3−(2
・2−ジクロロビニル)−2・2−ジメチルシクロプロ
パンカルボキシレート、 (R−5)α−シアノ−3−
フェノキシベンジル (IR・l5)−シス/トランス
−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レート、α−シアノ−3−フ
エノキシベンジルd−シス/トランスークリサンテマー
ト 1−エチニル−2−メチル−2−ペンテニル シス
/トランスークリサンテマート、1−エチニル−2−メ
チル−2−ペンテニル 2・2−ジメチル−3−(2メ
チル−コープロペニル)シクロプロパン−]カルボキシ
レート 1−エチニル−2−メチル−2ペンテニル 2
・2・3・3−テトラメチルシクロプロパンカルボキシ
レート、1−エチニル−2メチル−2−ペンテニル 2
・2−ジメチル−3(2・2−ジクロロビニル)シクロ
プロパン−1−カルボキシレート、 〔(ペンタフルオ
ロフェニル)−メチル]−1R,3R−3−(2,2−
ジクロロビニル)−2,2−ジメチル−シクロプロパン
カルボキシレート、0−0−ジメチル 0−(2・2−
ジクロロ)ビニルホスフェート、O−イソプロポキシフ
ェニルメチルカーバメート、o−O−ジメチルC)−(
3−メチル−4−二トロフェニル)チオノフォスフェー
ト、0−O−ジエチル 0−2−イソプロピル−4−メ
チル−ピリミジル−(6)−チオフォスフェート、0・
0−ジメチル 5−(1・2ジカルボエトキシエチル)
−ジチオフォスフェート等を例示できる。Furthermore, the mite control agent of the present invention may contain various insect repellents, synergists, pest repellents, rat repellents, antioxidants, decomposition inhibitors, bactericides, fungicides, fragrances, colorants, etc. You can also do it. As the insect repellent that can be blended, any of the various chemicals conventionally used for exterminating pests can be used. A typical drug is 3-allyl-2-methylcyclopent-2-
En-4-one-1yl dl-cis/trans-chrysanthemate 3-allyl-2-methylcyclopenta-2
-en-4-one-1-yl d-cis/trans-chrysanthemate d-3-allyl-2-methylcyclopent-2-en-4-one-1-yl d-) lance-chrysanthemate mate, 3-allyl-2-methylcyclopent-2-en-4-one-1-yl dtrans-chrysanthemate, N-(3,4,5,6-titrahydrophthalimido)-methyl dl- cis/trans-chrysanthemate, 5-benzyl 3-furylmethyl d-cis/trans-chrysanthemate, 5-(2-propargyl)-3-furylmethylchrysanthemate 3-phenoxybenzyl 2,2-dimethyl- 3-(2' ・2°-
dichloro)vinylcyclopropane hydroxylate, 3
-phenoxybenzyl d-cis/trans-chrysanthemate, α-cyanophenoxybenzyl isopropyl-4-chlorophenylacetate, (S)-α-cyano-3-phenoxybenzyl (IR・cis)3-(2
・2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate, (R-5)α-cyano-3-
Phenoxybenzyl (IR・l5)-cis/trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate, α-cyano-3-phenoxybenzyl d-cis/trans Santemate 1-ethynyl-2-methyl-2-pentenyl cis/trans-chrysantemate, 1-ethynyl-2-methyl-2-pentenyl 2,2-dimethyl-3-(2methyl-copropenyl)cyclopropane- ] Carboxylate 1-ethynyl-2-methyl-2pentenyl 2
・2,3,3-tetramethylcyclopropanecarboxylate, 1-ethynyl-2methyl-2-pentenyl 2
・2-dimethyl-3(2,2-dichlorovinyl)cyclopropane-1-carboxylate, [(pentafluorophenyl)-methyl]-1R,3R-3-(2,2-
dichlorovinyl)-2,2-dimethyl-cyclopropanecarboxylate, 0-0-dimethyl 0-(2,2-
dichloro)vinyl phosphate, O-isopropoxyphenylmethyl carbamate, o-O-dimethyl C)-(
3-Methyl-4-nitrophenyl)thionophosphate, 0-O-diethyl 0-2-isopropyl-4-methyl-pyrimidyl-(6)-thiophosphate, 0.
0-dimethyl 5-(1,2 dicarboethoxyethyl)
-dithiophosphate etc. can be exemplified.
本発明のダニ防除剤中の有効成分量は、その剤型、適用
方法、及び適用場所等に応じて適宜に決定すればよいが
、水和剤や乳剤の形態で用いる場合は、有効成分組成物
を0. 1〜50重量%、油剤やエアゾール剤の形態で
用いる場合は、有効成分組成物を011〜30重量%と
するのが好ましく、その適用量は、処理すべき面積1耐
当りに有効成分組成物を約100mg以上、適用空間1
rri’当りに有効成分組成物を約1.0mg以上存在
させるのが望ましい。The amount of active ingredient in the mite control agent of the present invention may be appropriately determined depending on its dosage form, application method, application location, etc. However, when used in the form of a wettable powder or emulsion, the active ingredient composition 0. When used in the form of oil or aerosol, it is preferable that the active ingredient composition be 0.1 to 30% by weight, and the amount to be applied is 0.1 to 30% by weight. Approximately 100mg or more, applicable space 1
It is desirable that the active ingredient composition is present in an amount of about 1.0 mg or more per rri'.
本発明はまた、上記ダニ防除剤を基材に保持させてなる
ダニ防除材をも提供するものである。該ダニ防除材は、
その基材の特性を利用してダニ防除性を有するフィルム
、シート建築・構築+2料等として用いられる。ここで
基材としては例えばポリエチレン、ポリプロピレン、ナ
イロン、ポリ塩化ビニル、ポリ塩化ビニリデン、ポリエ
ステル等の合成樹脂シート、動植物質又は無機質繊維体
シート(紙、布、不織布、皮革等)、これら合成樹脂と
無機質繊維又は粉体との混合シート又は混紡布、上記合
成樹脂と動植物繊維との混紡布又は不織布、アルミニウ
ム、ステンレス、亜鉛等の金属の箔又はフィルム及び上
記各種シートの積層シートを例示できる。さらに上記基
材としては、建築・構築材料とする天然木材例えばキリ
、ペンシルシダ、クス等やプラスチック例えば塩化ビニ
ル樹脂、塩素化ポリエチレン、ポリエチレン、ポリプロ
ピレン等の成型物をも有効に利用できる。これら基材へ
の本発明のダニ防除剤の保持手段は、特に制限はなく、
例えば塗布、含浸、滴下、混線等により行い得る。保持
量も特に制限はなく適宜に決定できるが、通常上記暴利
への含浸による場合は、飽和含浸量迄の量とするのが好
ましい。The present invention also provides a mite-controlling material in which the above-mentioned mite-controlling agent is retained in a base material. The tick control material is
Utilizing the characteristics of the base material, it is used as a film with dust mite repellent properties, a sheet construction/construction +2 material, etc. Here, the base material includes, for example, synthetic resin sheets such as polyethylene, polypropylene, nylon, polyvinyl chloride, polyvinylidene chloride, and polyester, animal and vegetable or inorganic fiber sheets (paper, cloth, nonwoven fabric, leather, etc.), and these synthetic resins. Examples include mixed sheets or blended fabrics with inorganic fibers or powder, blended fabrics or nonwoven fabrics with the above synthetic resins and animal and plant fibers, foils or films of metals such as aluminum, stainless steel, and zinc, and laminated sheets of the above various sheets. Further, as the above-mentioned base material, natural wood used as building and construction materials such as awn, pencil fern, oak, etc., and molded products of plastics such as vinyl chloride resin, chlorinated polyethylene, polyethylene, polypropylene, etc. can also be effectively used. The means for retaining the mite control agent of the present invention on these substrates is not particularly limited;
For example, it can be carried out by coating, impregnating, dropping, crossing, etc. The retained amount is also not particularly limited and can be determined as appropriate; however, in the case of impregnating the above-mentioned profiteers, it is preferable to set the amount up to the saturated impregnated amount.
〈発明の作用及び効果〉
以上に述べた如く本発明のダニ防除剤は、畳、カーペッ
ト、床、廊下、マツトレス、ソファ−1ぬいぐるみ、布
団や枕、毛布、シーツ等の寝具類、押入れ、収納具類、
倉庫等に載置、散布、噴霧、塗布、煙霧、加熱蒸散等の
方法により直接処理したり、又該防除剤を基材に保持さ
せたダニ防除材を上記の場所に設置すれば、優れたダニ
防除効果を示す。<Operation and Effects of the Invention> As described above, the mite control agent of the present invention can be used on tatami mats, carpets, floors, hallways, pine mattresses, sofa-1 stuffed animals, bedding such as futons, pillows, blankets, and sheets, closets, and storage. Ingredients,
If you directly treat it by placing it in a warehouse, spraying, spraying, painting, fogging, heating evaporation, etc., or if you install a tick control material with the insecticide in the base material in the above place, you can Shows mite control effect.
〈実施例〉 以下、本発明の実施例を挙げてさらに詳しく説明する。<Example> Hereinafter, the present invention will be explained in more detail with reference to Examples.
実施例1
コナヒヨウヒダニおよびケナガコナダニに対する効果試
験
試験方法
腰高シャーレ(Φ9cmX6cm)の蓋にろ紙(2Cm
X2cm)を貼り付け、これに有効成分をアセトンに
溶解して薬剤とし、該有効成分の含量が1mgないし1
0■になるよう薬剤を含浸させる。腰高シャーレ中に各
種のダニを100から200頭をいれ、先の処理紙を貼
付した蓋をもちいて密封する。2時間経過の時点で曝露
を中止し、曝露中止後24時間経過後に実体顕微鏡下で
各種ダニ類の生死を判定し、その結果を表1に示した。Example 1 Effect test on Dermatophagoides farinae and Dermatophagoides mite Test method A filter paper (2 cm
x 2 cm) and dissolve the active ingredient in acetone to make a drug, and the content of the active ingredient is 1 mg to 1.
Impregnate with the drug so that it becomes 0■. Place 100 to 200 mites of each type in a waist-high petri dish, and seal it using the lid covered with the treated paper. The exposure was stopped after 2 hours had elapsed, and 24 hours after the cessation of the exposure, the viability of each type of mite was determined under a stereomicroscope, and the results are shown in Table 1.
実施例2
250メツシユのナイロン製のゴース袋(6cm X1
2cm)に混紡綿2.5gをダニ培地0.2gと共にい
れた後、口を閉じてダニの逃亡を防止した状態の試料を
図1に示す(1)から(4)の位置に設置する。Example 2 250 mesh nylon goose bag (6cm x 1
After putting 2.5 g of mixed cotton together with 0.2 g of mite culture medium into a 2 cm), the sample was placed in positions (1) to (4) shown in FIG. 1 with the mouth closed to prevent mites from escaping.
その後90X50anの紙にdl−メントール1.6g
およびイソパラフィン0.4gを含浸させたものを(5
)から(10)の位置に設置して各種包装具を用いて2
5℃で4時間有効成分に曝露する。その後ゴース袋を取
りだし温度25℃、湿度74%に設定して1週間培養後
に飽和食塩水法にて生ダニ数を測定して増殖抑制率を求
め、その結果を表2に示す。Then dl-menthol 1.6g on 90x50an paper
and impregnated with 0.4 g of isoparaffin (5
) to (10) using various packaging tools.
Exposure to active ingredient for 4 hours at 5°C. Thereafter, the goose bag was taken out and cultured for one week at a temperature of 25° C. and a humidity of 74%, and then the number of live mites was measured using the saturated saline method to determine the growth inhibition rate. The results are shown in Table 2.
実施例3
dl−メント−ル30gに、香料を微量、イソパラフィ
ン20dを加え、さらにエタノールを加えて全体を27
0rdとし、これにジメチルエーテル30−と炭酸ガス
6gをエアゾール用耐圧缶(内容300Id)に充填し
て噴射装置に取付け、密封してエアゾール剤の形態とし
て本発明のダニ防除材を得た。Example 3 To 30 g of dl-menthol, add a small amount of fragrance and 20 d of isoparaffin, and then add ethanol to make the total 27 g.
0rd, and 30 g of dimethyl ether and 6 g of carbon dioxide gas were filled into an aerosol pressure-resistant can (content: 300 Id), attached to an injection device, and sealed to obtain the mite control material of the present invention in the form of an aerosol.
このようにして得た各エアゾールを用い、以下の試験を
行なった。The following tests were conducted using each of the aerosols thus obtained.
(試験方法)
ゴース袋(6X ]、 22cmに混紡綿2.5gをダ
ニ培地0.2gとともに入れた後、1」を閉じる。この
ゴース袋を敷布団と掛は布団(第2図で示した■〜■)
の各所に設置した後、下記のエアゾールを敷布団は両面
に15秒間ずつ、掛は布団は片面のみ20秒間処理し、
第2図に示したように、敷布団を三つ折りにし、掛は布
団で覆った状態で25°C下に4時間設置する。その後
、布団を陰干しして薬剤が完全に除去された時点でダニ
の入ったゴース袋を取り出し25°C1湿度74%下に
設置する。これを1週間後に飽和食塩水法によりダニだ
けを分離し、生ダニを数えてコントロール区に対する増
殖抑制率を求めた。(Test method) After putting 2.5 g of blended cotton together with 0.2 g of mite culture medium into a 22 cm Goose bag (6X), close the Goose bag. ~■)
After installing the following aerosol on each side of the futon, apply the following aerosol for 15 seconds on both sides of the futon, and for 20 seconds on one side of the futon.
As shown in Figure 2, the mattress was folded into three and placed under 25°C for 4 hours while covered with the futon. Thereafter, the futon is dried in the shade, and when the drug is completely removed, the goose bag containing the mites is taken out and placed at 25°C and 74% humidity. One week later, only the mites were separated using the saturated saline method, and the live mites were counted to determine the growth inhibition rate relative to the control group.
表3
表4
実施例4゜
エチレンメチルメタクリレート(メチルメタクリレート
20%含有)120部とdl−メントール20部を加え
]、 60″C下で押し出し成型を行ない。20X10
cm厚み1mmのシート(di−メントールとして約5
gを含有)を得た。Table 3 Table 4 Example 4 120 parts of ethylene methyl methacrylate (containing 20% methyl methacrylate) and 20 parts of dl-menthol were added] and extrusion molding was carried out at 60"C. 20X10
1 mm thick sheet (approximately 5 cm thick as di-menthol)
g) was obtained.
このようにして得られたシートを用い、以下の試験を行
なった。第3図に示したように布団袋(96X62X6
0cm)の中に敷布団と掛布団を各々3つ折りと4つ折
りにして収納する。250メツシユのナイロン製のゴー
ス袋(6cmX12cm)に混紡綿2゜5gをダニ培地
0.2gと共にいれた後、口を閉じてダニの逃亡を防止
した状態の試料を1〜3の位置に設置する。その後、上
記で得られたシートを4〜6の位置に設置して布団袋の
口を締め25℃下に置き、1週間後に飽和食塩水法にて
生ダニ数を測定して増殖抑制率を求め、その結果を表4
に示す。Using the sheet thus obtained, the following tests were conducted. As shown in Figure 3, a futon bag (96X62X6
0cm), fold the mattress into three and four, respectively, and store them. After putting 2.5 g of blended cotton together with 0.2 g of mite culture medium into a 250-mesh nylon goose bag (6 cm x 12 cm), place the sample in positions 1 to 3 with the mouth closed to prevent mites from escaping. . Thereafter, the sheet obtained above was placed in positions 4 to 6, the futon bag was closed, and the temperature was kept at 25°C. After one week, the number of live mites was measured using the saturated saline method to determine the growth inhibition rate. and the results are shown in Table 4.
Shown below.
実施例5
dl−メンI・−ル]O部を酸化ケイ素90部と充分撹
拌混合後粉状化して、粉末形態の本発明のダニ防除材を
得た。このようにして得た粉末剤を下記試験法により、
ダニ防除効果を試験した。なお比較としてd−メントー
ル、1−メントールを用いた以外は同様に粉剤を作製し
た。Example 5 Part of dl-menI.-L]O was sufficiently stirred and mixed with 90 parts of silicon oxide and then pulverized to obtain a powder form of the mite control material of the present invention. The powder thus obtained was tested according to the following test method.
The mite control effect was tested. For comparison, powders were prepared in the same manner except that d-menthol and 1-menthol were used.
く試験方法〉
約2cm長に切ったワラを加熱殺虫後、その5gを10
0mM三角フラスコに入れ、次に粉剤0.1g。Test method: Straw cut into approximately 2 cm length was heated to kill insects, and then 5 g of it was heated to 10
Pour 0mM into an Erlenmeyer flask, then add 0.1g of powder.
0.5gを投入し混合して、ポリ塩化ビニリデンフィル
ムで封をした後、25°C185〜90%RHの条件下
で1日保存する。この三角フラスコに約400頭のケナ
ガコナダニを投入し、同条件下で2日保存後、熱追い出
し法により生存ダニを追い出し、その数をカウントし、
死出率を下式により算出した。After adding 0.5 g and mixing, the mixture was sealed with polyvinylidene chloride film and stored for one day at 25° C. and 185 to 90% RH. Approximately 400 woolly mites were placed in this Erlenmeyer flask, and after storing them for 2 days under the same conditions, the surviving mites were expelled using the heat expulsion method, and their number was counted.
The mortality rate was calculated using the following formula.
その結果、本発明では、いずれの濃度でもほぼ100%
の死去率を得ることができ、十分なダニ防除性を示した
のに対し、比較のものはいずれの濃度もO〜30%程度
であった。As a result, in the present invention, almost 100%
It was possible to obtain a mortality rate of 1,000,000,000, and showed sufficient mite control properties, whereas in comparison, all concentrations were about 0 to 30%.
状態を示す。図中(])〜(3)は試料の設置位置を示
し、 (4)〜(6)は揮散性有効成分を有する支持体
の設置位置を示す。Indicates the condition. In the figure, (]) to (3) indicate the installation positions of the sample, and (4) to (6) indicate the installation positions of the support having the volatile active ingredient.
X;無処理区の生存ダニ数 y;処理区の生存ダニ数X: Number of surviving mites in untreated area y; Number of living mites in treated area
第1図は本発明の処理状態の実施態様の−・例を示す説
明図で、3つ折の敷布団(A)の上に4つ折の掛布団(
B)を載せた状態を示す。図中(1)〜(4)は試料の
設置位置を示し、 (5)〜(1o)は揮散性有効成分
を有する支持体の設置位置を示す。
第2図は本発明の処理状態の実施態様の他の一例を示す
説明図で、3つ折の敷布団(A)の上を掛布団(B)で
覆った状態を示す。図中(1)〜(3)は試料の設置位
置を示す。
第3図は本発明の処理状態の実施態様の更に他の一例を
示す説明図で、布団袋(C)の中で3つ折の敷布団(A
)の上に4つ折の掛布団(B)を載せた(以 上)
特許出願人 アース製薬株式会社
牙1図
矛2図
A、敷布団
B、掛布団
C1布団袋FIG. 1 is an explanatory diagram showing an example of the processing state of the present invention, in which a four-fold comforter (A) is placed on a three-fold mattress (A).
Shows the state in which B) is placed. In the figure, (1) to (4) indicate the installation positions of the sample, and (5) to (1o) indicate the installation positions of the support having the volatile active ingredient. FIG. 2 is an explanatory view showing another example of the embodiment of the processing state of the present invention, and shows a state in which a trifold mattress (A) is covered with a comforter (B). In the figure, (1) to (3) indicate the installation positions of the samples. FIG. 3 is an explanatory diagram showing still another example of the embodiment of the processing state of the present invention, in which the mattress (A) is folded in three in the futon bag (C).
) A four-folded comforter (B) was placed on top of the (above) Patent applicant: Earth Pharmaceutical Co., Ltd.
Claims (2)
分として含有することを特徴とするダニ防除剤。(1) A mite control agent containing dl-menthol and/or its isomer as an active ingredient.
請求項1に記載されたダニ防除材。(2) The mite control material according to claim 1, characterized in that the above-mentioned control agent is held in a carrier.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19450390A JPH0482805A (en) | 1990-07-23 | 1990-07-23 | Acarid control agent and acarid control material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19450390A JPH0482805A (en) | 1990-07-23 | 1990-07-23 | Acarid control agent and acarid control material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0482805A true JPH0482805A (en) | 1992-03-16 |
Family
ID=16325601
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP19450390A Pending JPH0482805A (en) | 1990-07-23 | 1990-07-23 | Acarid control agent and acarid control material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0482805A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2016153380A (en) * | 2015-02-20 | 2016-08-25 | アース製薬株式会社 | Activity enhancer of compound having menthane skeleton on pest |
-
1990
- 1990-07-23 JP JP19450390A patent/JPH0482805A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2016153380A (en) * | 2015-02-20 | 2016-08-25 | アース製薬株式会社 | Activity enhancer of compound having menthane skeleton on pest |
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