JPH04117305A - Acaricide - Google Patents
AcaricideInfo
- Publication number
- JPH04117305A JPH04117305A JP5467290A JP5467290A JPH04117305A JP H04117305 A JPH04117305 A JP H04117305A JP 5467290 A JP5467290 A JP 5467290A JP 5467290 A JP5467290 A JP 5467290A JP H04117305 A JPH04117305 A JP H04117305A
- Authority
- JP
- Japan
- Prior art keywords
- acaricide
- benzyl acetate
- active ingredient
- mites
- acaride
- 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
- 230000000895 acaricidal effect Effects 0.000 title claims abstract description 33
- 239000000642 acaricide Substances 0.000 title claims abstract description 26
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 claims abstract description 27
- 229940007550 benzyl acetate Drugs 0.000 claims abstract description 14
- 239000004480 active ingredient Substances 0.000 claims abstract description 9
- 239000000126 substance Substances 0.000 abstract description 8
- 241000238710 Dermatophagoides Species 0.000 abstract description 5
- 241001465754 Metazoa Species 0.000 abstract description 3
- 229920000742 Cotton Polymers 0.000 abstract description 2
- 239000000203 mixture Substances 0.000 abstract description 2
- 238000009834 vaporization Methods 0.000 abstract 2
- 241000916145 Tarsonemidae Species 0.000 abstract 1
- 230000008016 vaporization Effects 0.000 abstract 1
- 241000238876 Acari Species 0.000 description 19
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000002609 medium 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
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-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
- 239000002552 dosage form Substances 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 2
- SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 description 2
- 238000009395 breeding Methods 0.000 description 2
- 230000001488 breeding effect Effects 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 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
- 239000005995 Aluminium silicate Substances 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- 229920000858 Cyclodextrin Polymers 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
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- PWKSKIMOESPYIA-BYPYZUCNSA-N L-N-acetyl-Cysteine Chemical compound CC(=O)N[C@@H](CS)C(O)=O PWKSKIMOESPYIA-BYPYZUCNSA-N 0.000 description 1
- MMOXZBCLCQITDF-UHFFFAOYSA-N N,N-diethyl-m-toluamide Chemical compound CCN(CC)C(=O)C1=CC=CC(C)=C1 MMOXZBCLCQITDF-UHFFFAOYSA-N 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 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
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 239000013566 allergen Substances 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 208000006673 asthma Diseases 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- QUKGYYKBILRGFE-VJJZLTLGSA-N benzyl acetate Chemical class C[13C](=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-VJJZLTLGSA-N 0.000 description 1
- 229960002903 benzyl benzoate Drugs 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000007796 conventional method 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
- -1 diethyl-3-methylbenzamide (diethyl-3-methylbenzamide) Chemical compound 0.000 description 1
- 229960001673 diethyltoluamide Drugs 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 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
- 235000013312 flour Nutrition 0.000 description 1
- 238000003958 fumigation Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 230000000749 insecticidal effect Effects 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
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000003915 liquefied petroleum gas Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 229960000969 phenyl salicylate Drugs 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 229940100445 wheat starch Drugs 0.000 description 1
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) 本発明は新規な投ダニ剤に関する。[Detailed description of the invention] (Industrial application field) The present invention relates to a novel acaricide.
(従来の技術)
近年の生活様式の変化に伴い、屋内でダニが大量に発生
するようになり、大きな問題となっている。例えば、カ
ーペット、布団等に発生し、棲息するチリダニは、喘息
等のアレルゲンとなり、健康上の大きな脅威となってい
る。また、畳に棲息するコナダニ類は健康に直接の害は
ないものの不快感を伴い、ツメダニの大発生を誘発する
因子となっている。(Prior Art) With changes in lifestyles in recent years, a large number of mites have been occurring indoors, which has become a major problem. For example, dust mites that appear and live on carpets, bedding, and the like become allergens for asthma and other conditions, and pose a major health threat. Furthermore, although the mites that live on tatami mats do not pose a direct threat to health, they cause discomfort and are a factor that induces large outbreaks of mites.
従来、屋内に棲息するダニを防除するために、フェニト
ロチオン、フェンチオン、DDVP、ダイアジノン等の
リン酸系化合物、プロポクサーNAC等のカーバメイト
系化合物、その他、サリチル酸フェニル、安息香酸ベン
ジル、DEET(N、N−ジエチル−3−メチルベンザ
ミド)等の種々の薬剤が用いられている。Conventionally, in order to control mites living indoors, phosphate compounds such as fenitrothion, fenthion, DDVP, diazinon, carbamate compounds such as propoxer NAC, phenyl salicylate, benzyl benzoate, DEET (N, N- Various drugs have been used, such as diethyl-3-methylbenzamide (diethyl-3-methylbenzamide).
(発明が解決しようとする課題)
しかし、上記のダニ防除薬剤はいずれも、毒性が高かっ
たり、高価であったり、一定の範囲のダニにしか効かな
い等の欠点があった。(Problems to be Solved by the Invention) However, all of the above-mentioned mite control agents have drawbacks such as being highly toxic, expensive, and effective only against a certain range of mites.
またこれらの薬剤は、ダニと接触しなければ効果が出現
しないため、その効果を発揮させるためには断続的に処
理するとか、畳の内部を処理する場合には薬剤注入を万
遍なく行わなければならないという欠点があった。In addition, these chemicals are not effective unless they come into contact with mites, so in order for them to be effective, they must be treated intermittently, or when treating the inside of tatami, the chemicals must be injected evenly. There was a drawback that it had to be done.
(課題を解決するための手段)
本発明者は、新規な殺ダニ剤を得べく1種々の化合物に
ついて、そのダニに対する薬理作用を検索していたとこ
ろ、ベンジルアセテートは優れた殺ダニ効果を有し、し
かも従来のダニ防除薬剤の欠点を解消するものであるこ
とを見出し本発明を完成した。(Means for Solving the Problems) The present inventor was searching for the pharmacological action of various compounds against mites in order to obtain a new acaricide, and found that benzyl acetate has an excellent acaricidal effect. However, the present invention was completed based on the discovery that it overcomes the drawbacks of conventional mite control agents.
すなわち本発明は、ベンジルアセテートを有効成分とし
て含有する殺ダニ剤を提供するものである。That is, the present invention provides an acaricide containing benzyl acetate as an active ingredient.
本発明の殺ダニ剤は、このベンジルアセテートを公知の
液体または固体担体と組合せ配合し、油剤、乳剤、水和
剤、噴霧剤、エアゾール剤、粉剤粒剤、薫蒸剤、蒸散剤
等適当な剤形とすることにより調整される。The acaricide of the present invention is prepared by combining this benzyl acetate with a known liquid or solid carrier, and then using a suitable agent such as an oil solution, emulsion, wettable powder, spray, aerosol, powder, granule, fumigation agent, or evaporation agent. It is adjusted by making it into a dosage form.
使用することのできる液体担体の例としては、水、メタ
ノール、エタノール、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
。Examples of liquid carriers that can be used include water, alcohols such as methanol, ethanol, and isopropyl alcohol, ketones such as acetone, methyl ethyl ketone, and cyclohexanone, ethers such as tetrahydrofuran, dioxane, and dimethyl ether, hexane, kerosene, and n. Aliphatic hydrocarbons such as paraffin and solvent naphtha, aromatic hydrocarbons such as benzene and toluene.
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が挙げ
られる。Examples include halogenated hydrocarbons such as dichloromethane and dichloroethane, and esters such as ethyl acetate and butyl acetate.
また、固体担体の例としては、ケイ酸、カオリン、活性
炭、ベントナイト、ケイソウ土、タルク。Examples of solid carriers include silicic acid, kaolin, activated carbon, bentonite, diatomaceous earth, and talc.
クレー、炭酸カルシウム等の無機粉末、大豆粉、小麦粉
5デンプン等の植物粉末、シクロデキストリン等の包接
化合物が挙げられる。Examples include inorganic powders such as clay and calcium carbonate, plant powders such as soybean flour and wheat starch, and clathrate compounds such as cyclodextrin.
本発明の殺ダニ剤には、さらに剤形およびその必要に応
じて乳化剤、分散剤、展着剤、安定剤、噴射剤、揮散調
整剤を添加することもできる。The acaricide of the present invention may further contain emulsifiers, dispersants, spreading agents, stabilizers, propellants, and volatilization regulators depending on the dosage form and its necessity.
叙上の如くして得られた本発明の殺ダニ剤中の有効成分
量は、剤形、使用方法、使用場所等に応じて調整するこ
とが可能であるが、一般には組成物中、0.1〜80重
量%程度、特に1〜40重量%重量上程ることが望まし
い。The amount of active ingredient in the acaricide of the present invention obtained as described above can be adjusted depending on the dosage form, method of use, place of use, etc., but in general, 0. .1 to 80% by weight, particularly 1 to 40% by weight is desirable.
本発明の殺ダニ剤で好ましい殺ダニ効果を得るためには
、例えばカーペット等に散布する場合、1平方メートル
当たり有効成分として20■程度以上散布すれば良い。In order to obtain a preferable acaricidal effect with the acaricide of the present invention, for example, when spraying on a carpet or the like, it is sufficient to apply the active ingredient at a rate of about 20 μm or more per square meter.
なお、本発明の殺ダニ剤の有効成分であるベンジルアセ
テートはそれ自体で揮散して殺ダニ作用を有するので、
散布すべき部屋の広さに見あった表面積を有する組成物
とし、自己揮散作用のみによって連続的に散布させるこ
とが可能であり1便利である。こうすることにより、例
えば畳中のダニに対しても従来より少ない薬剤注入箇所
で充分な効果が期待できる。また、布団等の寝具類のダ
ニに対しても薬剤を揮散させることにより効果的に布団
綿中のダニを防除し得るし、揮散が早い点から、処理後
の残留薬剤も短時間に除去し得る。In addition, benzyl acetate, which is the active ingredient of the acaricide of the present invention, volatilizes by itself and has acaricidal action.
The composition has a surface area commensurate with the size of the room to be sprayed, and is convenient because it can be sprayed continuously only by self-volatilization. By doing so, a sufficient effect can be expected on, for example, mites in tatami mats with fewer injection points than before. In addition, it is possible to effectively control mites in bedding such as futons by volatilizing the chemical, and since the volatilization is quick, any residual chemical after treatment can be removed in a short time. obtain.
(作用および発明の効果)
本発明の殺ダニ剤の有効成分であるベンジルアセテート
は、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、ケナガコナダニのコナダニ類に対し優れた作用
を有し、しかも天然成分であって、人や動物に対して安
全性の高いものである。(Actions and Effects of the Invention) Benzyl acetate, which is an active ingredient of the acaricide of the present invention, has an excellent action against the Dermatophagoides mites such as Dermatophagoides nigricans and Dermatophagoides nigricans, as well as the Dermatophagoides mites, and is a natural ingredient. It is highly safe for humans and animals.
従って、本発明の殺ダニ剤は、畳、カーペット、床、廊
下等の室内を始め、マツトレス、布団、枕等の寝具、ソ
ファ−1収納具等の家具等に適用することにより、安全
かつ有効にダニ類を駆除することができる。Therefore, the acaricide of the present invention can be applied safely and effectively to indoor areas such as tatami mats, carpets, floors, and hallways, bedding such as pine mattresses, futons, and pillows, and furniture such as sofa-1 storage equipment. can exterminate mites.
特に、ベンジルアセテートの自己揮散能を利用した殺ダ
ニ剤によれば、容易に短時間で室内のダニを駆除するこ
とができるので極めて有利である。In particular, acaricides that utilize the self-volatile ability of benzyl acetate are extremely advantageous because they can easily exterminate indoor mites in a short time.
(実施例)
次ぎに実施例、試験例を挙げ、本発明をさらに詳しく説
明する。(Example) Next, the present invention will be explained in more detail by giving Examples and Test Examples.
実施例 1
殺ダニ試験
ケナガコナダニ(■諺吐■■putrescentia
e)を供試虫として用い、下に示すドライフィルム法で
本発明の殺ダニ剤の効果を調べた。Example 1 Acaricidal test
e) was used as a test insect, and the effect of the acaricide of the present invention was investigated by the dry film method shown below.
この試験結果を第1表に示す。The test results are shown in Table 1.
K簾方亘
(1)ドライフィルム法
ガラス製バイアル(直径1cn、高さ6dl)にアセト
ンで所定濃度に希釈した薬剤を一定量入れた。Wataru Krenkata (1) Dry film method A fixed amount of a drug diluted with acetone to a predetermined concentration was placed in a glass vial (diameter 1 cn, height 6 dl).
薬剤を容器内面に均一に付着させ、アセトンを揮散させ
た後、所定数のケナガコナダニを入れ、通気性テフロン
ラップで口を塞いだ。After the chemical was applied uniformly to the inner surface of the container and the acetone was volatilized, a predetermined number of woolly mites were placed in the container, and the mouth was closed with breathable Teflon wrap.
−区二連とし、相対湿度75%、温度25℃の条件下で
保管し、−日後の致死率をI[察した。The cells were stored in duplicate under conditions of relative humidity of 75% and temperature of 25°C, and the mortality rate after - days was measured.
蟇−困
第
表
実施例 2
揮散作用による殺ダニ効果
直径5.51のろ紙に薬剤を含浸させ、同径のシャーレ
に入れた。一方、それぞれのバイアル(直径3alI、
高さ6aa)にケナガコナダニとヤケヒヨウヒダニ(D
ermato ha oides teronyss
ius)の繁殖培地を入れ、口を通気性ラップで塞いだ
。Toad Trouble Table Example 2 Acaricidal effect by volatilization effect A filter paper with a diameter of 5.5 mm was impregnated with a chemical and placed in a petri dish of the same diameter. Meanwhile, each vial (diameter 3alI,
Height 6 aa)
ermato haoides teronyss
ius) propagation medium was added, and the mouth was closed with breathable plastic wrap.
500s+4のフラスコにそれぞれのダニバイアルと薬
剤のシャーレを入れ、フラスコの口をラップで密閉した
。−日放置後にダニの生死を観察し、薬剤の揮散による
殺ダニ活性を判定した。この結果を第2表に示す。Each mite vial and drug petri dish were placed in a 500s+4 flask, and the mouth of the flask was sealed with plastic wrap. - After being left for a day, the mites were observed to be alive or dead, and the acaricidal activity by volatilization of the chemical was determined. The results are shown in Table 2.
第 2 表
この結果から明らかなように、ベンジルアセテートは従
来の殺ダニ剤と異なり、その揮散成分に強力な殺虫活性
を有している。Table 2 As is clear from the results, benzyl acetate has strong insecticidal activity in its volatile components, unlike conventional acaricides.
実施例 3
スプレー型殺ダニ剤
20gのベンジルアセテート、130gのエタノールお
よび150gの液化石油ガスを常法に従いエアゾール用
耐圧缶に充填して殺ダニ剤を得た。Example 3 Spray-type acaricide 20 g of benzyl acetate, 130 g of ethanol, and 150 g of liquefied petroleum gas were filled into an aerosol pressure can according to a conventional method to obtain an acaricide.
実施例 4
シート型殺ダニ剤
直径11(!lのろ紙にベンジルアセテート0.5gを
含浸させて殺ダニシートを得た。Example 4 Sheet type acaricide A miticide sheet was obtained by impregnating a filter paper with a diameter of 11 (!l) with 0.5 g of benzyl acetate.
試験例 1
1Qのフラスコにケナガコナダニの繁殖培地0゜5gを
入れ、これに実施例3で得た殺ダニ剤を3秒間スプレー
した。1日放置後に培地の一部を取り、殺ダニ率を測定
したところ、はぼ100%の殺ダニ率であった。Test Example 1 A 1Q flask was filled with 0.5 g of a propagation medium for the mites, and the acaricide obtained in Example 3 was sprayed onto the flask for 3 seconds. After leaving it for one day, a portion of the culture medium was taken and the acaricidal rate was measured, and the acaricidal rate was approximately 100%.
試験例 2
ガラス容器内に実施例4で得た殺ダニシートを敷き、そ
の上に8X8mのカーペットを置いてケナガコナダニの
繁殖培地0.5gを加えた。蓋をして1日放置後に生き
ダニ数を測定してダニ防除率を求めた。この結果、ダニ
防除率はほぼ100%であり充分な効力が得られた。Test Example 2 The acaricidal sheet obtained in Example 4 was placed in a glass container, an 8 x 8 m carpet was placed on top of the sheet, and 0.5 g of a breeding medium for woolly mites was added. After leaving the lid on for one day, the number of live mites was measured to determine the mite control rate. As a result, the mite control rate was almost 100%, and sufficient efficacy was obtained.
試験例 3
ガラス容器内に実施例4で得た殺ダニシートを敷き、そ
の上に綿2gを入れた。これにケナガコナダニの繁殖培
地1gを加え、蓋をして1日放置後に生きダニ数を測定
してダニ防除率を求めた。Test Example 3 The mite-killing sheet obtained in Example 4 was placed in a glass container, and 2 g of cotton was placed on top of it. To this was added 1 g of a breeding medium for woolly mites, and after leaving it for one day with a lid on, the number of living mites was measured to determine the mite control rate.
この結果、ダニ防除率はほぼ100%であり、充分な効
力を示した。As a result, the mite control rate was almost 100%, indicating sufficient efficacy.
以 上that's all
Claims (1)
。Acaricide containing benzyl acetate as an active ingredient.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5467290A JP2897054B2 (en) | 1990-03-06 | 1990-03-06 | Acaricide |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5467290A JP2897054B2 (en) | 1990-03-06 | 1990-03-06 | Acaricide |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04117305A true JPH04117305A (en) | 1992-04-17 |
JP2897054B2 JP2897054B2 (en) | 1999-05-31 |
Family
ID=12977276
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5467290A Expired - Lifetime JP2897054B2 (en) | 1990-03-06 | 1990-03-06 | Acaricide |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2897054B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001000033A1 (en) * | 1999-06-28 | 2001-01-04 | Ecosmart Technologies, Inc. | Plant essential oils against dust mites |
US6689395B2 (en) * | 1999-06-28 | 2004-02-10 | Ecosmart Technologies, Inc. | Pesticidal compositions containing plant essential oils against mites |
-
1990
- 1990-03-06 JP JP5467290A patent/JP2897054B2/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001000033A1 (en) * | 1999-06-28 | 2001-01-04 | Ecosmart Technologies, Inc. | Plant essential oils against dust mites |
US6689395B2 (en) * | 1999-06-28 | 2004-02-10 | Ecosmart Technologies, Inc. | Pesticidal compositions containing plant essential oils against mites |
Also Published As
Publication number | Publication date |
---|---|
JP2897054B2 (en) | 1999-05-31 |
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