JPH03106805A - Acaricide - Google Patents
AcaricideInfo
- Publication number
- JPH03106805A JPH03106805A JP24083589A JP24083589A JPH03106805A JP H03106805 A JPH03106805 A JP H03106805A JP 24083589 A JP24083589 A JP 24083589A JP 24083589 A JP24083589 A JP 24083589A JP H03106805 A JPH03106805 A JP H03106805A
- Authority
- JP
- Japan
- Prior art keywords
- ylang
- mites
- acaricide
- oil
- rooms
- 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
- 230000000895 acaricidal effect Effects 0.000 title claims abstract description 32
- 239000000642 acaricide Substances 0.000 title claims abstract description 27
- 240000007436 Cananga odorata Species 0.000 claims abstract description 15
- 239000004480 active ingredient Substances 0.000 claims abstract description 8
- 241000238876 Acari Species 0.000 abstract description 33
- 239000003921 oil Substances 0.000 abstract description 12
- 230000000694 effects Effects 0.000 abstract description 6
- 239000002552 dosage form Substances 0.000 abstract description 4
- 239000000428 dust Substances 0.000 abstract description 4
- 241000209140 Triticum Species 0.000 abstract description 3
- 235000021307 Triticum Nutrition 0.000 abstract description 3
- 239000000443 aerosol Substances 0.000 abstract description 3
- 235000013312 flour Nutrition 0.000 abstract description 3
- 239000007788 liquid Substances 0.000 abstract description 3
- 238000002156 mixing Methods 0.000 abstract description 3
- 239000007787 solid Substances 0.000 abstract description 3
- 239000005995 Aluminium silicate Substances 0.000 abstract description 2
- 150000001298 alcohols Chemical class 0.000 abstract description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 abstract description 2
- 235000012211 aluminium silicate Nutrition 0.000 abstract description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract description 2
- 239000000839 emulsion Substances 0.000 abstract description 2
- 239000008187 granular material Substances 0.000 abstract description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 abstract description 2
- 239000000203 mixture Substances 0.000 abstract description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 2
- 239000004563 wettable powder Substances 0.000 abstract description 2
- 241000132125 Tyrophagus Species 0.000 abstract 1
- 230000001747 exhibiting effect Effects 0.000 abstract 1
- 239000002316 fumigant Substances 0.000 abstract 1
- 238000001256 steam distillation Methods 0.000 abstract 1
- 239000002609 medium Substances 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 238000009395 breeding Methods 0.000 description 5
- 230000001488 breeding effect Effects 0.000 description 5
- 241000238710 Dermatophagoides Species 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000000843 powder 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
- -1 DDvP Chemical compound 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
- 239000003814 drug Substances 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000007921 spray 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
- 229920000742 Cotton Polymers 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- 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 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 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
- 239000000969 carrier Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000004033 plastic 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
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- 235000007571 Cananga odorata Nutrition 0.000 description 1
- 229920000858 Cyclodextrin Polymers 0.000 description 1
- 208000030453 Drug-Related Side Effects and Adverse reaction Diseases 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
- 241001465754 Metazoa Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 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
- 206010070863 Toxicity to various agents Diseases 0.000 description 1
- 239000013566 allergen Substances 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
- 229960002903 benzyl benzoate Drugs 0.000 description 1
- 239000011575 calcium Substances 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
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000002537 cosmetic Substances 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
- 229960001673 diethyltoluamide Drugs 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 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
- 239000003205 fragrance Substances 0.000 description 1
- 238000003958 fumigation Methods 0.000 description 1
- 230000009036 growth inhibition Effects 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
- 230000005764 inhibitory process Effects 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
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000003915 liquefied petroleum gas Substances 0.000 description 1
- 230000003129 miticidal effect Effects 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical class OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 1
- 125000002467 phosphate group Chemical class [H]OP(=O)(O[H])O[*] 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- VEMKTZHHVJILDY-FIWHBWSRSA-N resmethrin Chemical compound CC1(C)[C@H](C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-FIWHBWSRSA-N 0.000 description 1
- 229940108410 resmethrin Drugs 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
- 239000000344 soap Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000010998 test method Methods 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
- 230000009466 transformation Effects 0.000 description 1
- 230000005068 transpiration Effects 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
Abstract
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明は新規な殺ダニ剤に関する。[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ない、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、
カーベット、布団等に発生し、棲息するダニは、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、畳に生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ない、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, futons, etc. become allergens for asthma and other conditions, and pose a major health threat. Furthermore, although the mites that live on tatami mats are not directly harmful 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、フエンチオン、DDvP、ダイアジノン等の
リン酸系化合物、プロボクサー、NAC等のカーバメイ
ト系化合物、レスメトリンフォルテ等のビレスロイド系
化合物、その他、サリチル酸フエニル、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, and diazinon, carbamate compounds such as Proboxer and NAC, birethroid compounds such as resmethrin forte, and other phenyl salicylates have been used. , benzyl benzoate, and DEET (N,N-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、何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, the above-mentioned mite control agents all 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
遍なく行な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 mats, the chemicals must be injected evenly. There was a drawback that it had to be done.
更に、布団等の寝具類のダニ防除に関しても、残留する
薬剤毒性の問題から実際の使用には不安があった。Furthermore, regarding the control of mites on bedding such as futons, there has been concern about the actual use of these bedding products due to the problem of residual drug toxicity.
[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、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、バンレイシ科に属するカナンガ・オドラタ( Ca
nangiumodorata foriageniu
m)の花を水蒸気蒸溜して得られるイランイラン油は優
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] In order to obtain a new acaricide, the present inventor was searching for the pharmacological action of various compounds against mites, and found that Cananga odorata (Ca.
nangiumodorata foriageniu
The present invention was completed based on the discovery that ylang-ylang oil obtained by steam distilling the flowers of (m) has an excellent acaricidal effect and also overcomes the drawbacks of conventional mite control agents.
すなわち本発明は、イランイラン油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 ylang-ylang oil as an active ingredient.
本発明の殺ダニ剤において有効成分として用いられるイ
ランイラン油は、すでに公知の化合物であり、高級化粧
品や石鹸の香料として用いられている化合物である。Ylang-ylang oil, which is used as an active ingredient in the acaricide of the present invention, is a well-known compound that is used as a fragrance in high-end cosmetics and soaps.
本発明の殺ダニ剤は、このイランイラン油を公知の液体
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、くん蒸剤、蒸散剤
等適当な剤形とすることにより調製される。The acaricide of the present invention can be prepared by combining this ylang-ylang oil with a known liquid or solid carrier, such as an oil solution, an emulsion, a wettable powder,
It is prepared by preparing a suitable dosage form such as a spray, an aerosol, a powder, a granule, a fumigation agent, or a transpiration agent.
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、イソプロビルアルコール等のアル
コール: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、ソルペ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が挙げ
られる。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; tetrahydrofuran, dioxane,
Ethers such as dimethyl ether; aliphatic hydrocarbons such as hexane, kerosene, normal paraffin, and solpent naphtha; aromatic hydrocarbons such as benzene and toluene;
Examples include halogenated hydrocarbons such as dichloromethane and dichloroethane; 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、クレー、炭酸
カルシュウム等の無機粉末;大豆粉、小麦粉、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 of solid carriers include inorganic powders such as silicic acid, kaolin, activated carbon, bentonite, diatomaceous earth, talc, clay, and calcium carbonate; vegetable powders such as soybean flour, wheat flour, and starch; and clathrate compounds such as cyclodextrin. can be mentioned.
本発明の殺ダニ剤には、更に剤形及びその必要に応じて
乳化剤、分散剤、展着剤、安定剤、噴射剤、揮敢調製剤
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 volatile preparation agents 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%程度とすることが望まし
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. It is desirable that the content be about 1 to 80% by weight, particularly about 1 to 40% by weight.
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
当り有効成分として20mg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 spray at least about 20 mg of the active ingredient per square meter.
なお、本発明殺ダニ剤の有効成分であるイランイラン油
はそれ自身でtl敗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合った表面積を有する組成物とし
、自己揮敢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、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
十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敢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, since ylang-ylang oil, which is the active ingredient of the acaricide of the present invention, has a miticidal effect by itself, the composition should have a surface area commensurate with the size of the room where it is to be sprayed. Continuous dispersion is possible and convenient by action alone. By doing this, it is possible to expect a sufficient effect against, for example, mites in tatami mats, with fewer injection points than before. In addition, by applying the chemical to futons and other bedding, it is possible to effectively control the dust mites in the futon cotton, and since the chemical evaporates quickly, any residual chemical after treatment can be removed in a short time. It is possible.
[作用及び発明の効果]
本発明殺ダニ剤の有効成分であるイランイラン油は、コ
ナヒョウヒダニやケヒョウヒダニ等のヒョウヒダニ類、
ケナガコナダニやムギコナダニ等のコナダニ類等に対し
優れた作用を有し、しかも天然成分であって、人や動物
に対する安全性の高いものである。[Action and Effect of the Invention] Ylang-ylang oil, which is the active ingredient of the acaricide of the present invention, is effective against the mites such as Dermatophagoides nigricans and Dermatophagoides,
It has an excellent effect on mites such as woolly mites and wheat mites, and is a natural ingredient that is highly safe for humans and animals.
したがって、本発明の殺ダニ剤は、畳、カーベット、床
、廊下等の室内を始め、マットレス、布団、枕等の寝具
、ソファー、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 not only to indoor areas such as tatami mats, carpets, floors, and hallways, but also to bedding such as mattresses, futons, pillows, and furniture such as sofas and storage utensils.
Mites can be exterminated safely and effectively.
特に、イランイラン油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 ylang-ylang oil are extremely advantageous because they can easily exterminate indoor mites in a short period of time.
[実施例]
次に実施例、試験例を挙げ、本発明を更に詳しく説明す
る。[Example] Next, the present invention will be explained in more detail by giving Examples and Test Examples.
実施fRl
殺ダニ試験:
ヤケヒヒョウダニ( Dermatophagoide
spteronyssius )およびケナガコナダニ
(Tyrophagus putrescentiae
)を供試虫として用い、下に示すドライフィルム法およ
び培地混入法で本発明殺ダニ剤の効果を調べた。Conducted fRl acaricidal test: Dermatophagoide
spteronyssius) and the woolly mite (Tyrophgus putrescentiae)
) was used as a test insect, and the effect of the acaricide of the present invention was investigated using the dry film method and medium mixing method shown below.
この試験結果を第 1 表および第2表に示す。The test results are shown in Tables 1 and 2.
試験方法:
(1) ドライフィルム法
ガラス製パイアル(直径1cm、高さ6備)にアセトン
で所定濃度に希釈した薬剤を一定量入れた。薬剤を容器
内面に均一に付着させ、アセトンを揮敗させた後、所定
数のダニを入れ、通気性テフロンラップで口を塞いだ。Test method: (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 cm, height 6 tubes). After the chemical was applied uniformly to the inner surface of the container and the acetone was volatilized, a predetermined number of mites were placed in the container, and the mouth was closed with breathable Teflon wrap.
一区三連とし、相対湿度90%、温度25℃の条件下で
保管し、一日後の致死率を観察した。Each plot was set in triplicate and stored under conditions of relative humidity of 90% and temperature of 25°C, and the mortality rate was observed after one day.
(2)培地混入法
含水率を15%程度にmt!シた粉末試料培地に供試試
料を1%となるように混合した。(2) Medium mixing method: Reduce the moisture content to around 15%! The test sample was mixed into the powdered sample medium at a concentration of 1%.
この混合培地5gをバイアル(直径3 am、高さ6
cm )に入れ、次にダニの繁殖培地を0.1g植え付
け、軽く混合した。 バイアルの口を通気性ラップで塞
ぎ、相対湿度90%、温度25℃の条件下で保管した。5 g of this mixed medium was placed in a vial (diameter 3 am, height 6
cm) and then inoculated with 0.1 g of mite breeding medium and mixed gently. The mouth of the vial was closed with air-permeable wrap and stored under conditions of relative humidity of 90% and temperature of 25°C.
ケナガコナダニについては1週間後に、ヤケヒョウヒダ
ニについては2週間後にそれぞれ培地0.1gを取り、
食塩水浮遊法で生きダニ数を数え、全体数を推定し、次
式により増殖抑制率を求めて効力を判定した。一区二連
とし、ダニ数のカウントは二回ずつ行った●増殖抑11
J!1!(!)= ( 1−T/C) X 1 0 0
C: 対照区の単位重量当りのダニ数
T: 処理区の単位重量当りのダニ数
結
果:
第
1
表
(以下余白)
第 2!Ii
供拭試料 ケナがコナダニ
ャケヒきウヒダニ実施例2
#1l散作用による殺ダニ効果:
直径5 . 5 ellのろ紙に薬剤を含浸させ、同径
のシャーレに入れて、口を掃除機用ゴミバックに使用さ
れている紙で覆った。 一方、それぞれのパイアル(直
径3cI1、高さ6 Cl1 )にケナガコナダニとヤ
ケヒョウヒダニの繁殖培地を入れ、口を通気性ラップで
塞いだ。0.1 g of the medium was taken after one week for the woolly mites, and after two weeks for the mites.
The number of live mites was counted using the saline suspension method, the total number was estimated, and the growth inhibition rate was calculated using the following formula to determine efficacy. Each section was divided into two series, and the number of mites was counted twice. ●Proliferation inhibition 11
J! 1! (!) = (1-T/C) X 1 0 0
C: Number of mites per unit weight in control area T: Number of mites per unit weight in treated area Results: Table 1 (margins below) 2nd! Ii Wipe sample Kena is Konada mite
Mite-killing effect of #1l powder: Diameter 5. A 5-cell filter paper was impregnated with the drug, placed in a petri dish of the same diameter, and the mouth was covered with paper used for a garbage bag for a vacuum cleaner. On the other hand, a breeding medium for woolly mites and Dermatophagoides mites was placed in each vial (diameter 3 cI1, height 6 Cl1), and the mouth was closed with breathable plastic wrap.
I KE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。
一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3表番ご示す。Each tick vial and drug petri dish were placed in an IKE flask, and the mouth of the flask was sealed with plastic wrap.
After leaving it for one day, the mites were observed to see if they were alive or dead, and the acaricidal activity by volatilization of the chemical was determined. The results are shown in Table 3.
第
3
表
二の結果から明らかなように、イランイラン油は従来の
殺ダニ剤と異なり、その揮散戒分にも強力な殺虫活性を
有している。As is clear from the results in Table 3, ylang-ylang oil has strong insecticidal activity even in its volatile components, unlike conventional acaricides.
実施例3
スプレー型殺ダニ剤:
20gのイランイラン油、130gのエタノール及び1
50g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 acaricide: 20g ylang-ylang oil, 130g ethanol and 1
A miticide was obtained by filling 50 g of liquefied petroleum gas into an aerosol pressure can according to a conventional method.
実施例4 シート型殺ダニ剤: 直径11cmのろ紙にイランイラン油 0.5gを含浸させて殺ダニシ一トを得た。Example 4 Sheet type acaricide: Ylang-ylang oil on a filter paper with a diameter of 11 cm Acaricide was obtained by impregnating 0.5 g.
試験例 l
1 ?Zのフラスコにケナガコナダニの繁殖培地0.5
g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、ほぼ100%の殺ダニ率であった。Test example l 1? 0.5 of woolly mite breeding medium in Z flask
g, and the acaricide obtained in Example 3 was sprayed thereon 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で得た殺ダニシ一トを敷き、そ
の上に8X8cm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
ダニ数を測定してダニ防除率を求めた。 この結果、ダ
ニ防除車はほぼ100%であり十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 8x8 cm carpet was placed on top of it, 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 dust 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で得た殺ダニシ一トを敷き、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日放置後に生ダニ数を測定
してダニ防除車を求めた。 この結果、ダニ防除率はほ
ぼ100%であり、十分な効力を示した。Test Example 3 The acaricidal sheet obtained in Example 4 was placed in a glass container, and 2 g of cotton was placed on top of it. To this, 1 g of a breeding medium for woolly mites was added, and after leaving it for one day with a lid on, the number of living mites was measured to obtain a mite control vehicle. As a result, the mite control rate was almost 100%, indicating sufficient efficacy.
以 上 出 願 人 エ ス ア 化 学 株式会社Below Up Out wish Man workman vinegar a transformation studies Co., Ltd.
Claims (1)
剤。(1) Acaricide containing ylang-ylang oil as an active ingredient.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24083589A JPH03106805A (en) | 1989-09-19 | 1989-09-19 | Acaricide |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24083589A JPH03106805A (en) | 1989-09-19 | 1989-09-19 | Acaricide |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03106805A true JPH03106805A (en) | 1991-05-07 |
Family
ID=17065407
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP24083589A Pending JPH03106805A (en) | 1989-09-19 | 1989-09-19 | Acaricide |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03106805A (en) |
-
1989
- 1989-09-19 JP JP24083589A patent/JPH03106805A/en active Pending
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