JPH03258705A - Miticide - Google Patents
MiticideInfo
- Publication number
- JPH03258705A JPH03258705A JP5467190A JP5467190A JPH03258705A JP H03258705 A JPH03258705 A JP H03258705A JP 5467190 A JP5467190 A JP 5467190A JP 5467190 A JP5467190 A JP 5467190A JP H03258705 A JPH03258705 A JP H03258705A
- Authority
- JP
- Japan
- Prior art keywords
- agent
- action
- mites
- effect
- miticide
- 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
- 239000000642 acaricide Substances 0.000 title claims abstract description 17
- 150000001875 compounds Chemical class 0.000 claims abstract description 10
- 230000000895 acaricidal effect Effects 0.000 claims description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 239000004480 active ingredient Substances 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- 241000238876 Acari Species 0.000 abstract description 15
- 239000003795 chemical substances by application Substances 0.000 abstract description 11
- 125000000217 alkyl group Chemical group 0.000 abstract description 6
- 230000000694 effects Effects 0.000 abstract description 5
- 239000000843 powder Substances 0.000 abstract description 5
- 241000238710 Dermatophagoides Species 0.000 abstract description 4
- 239000007788 liquid Substances 0.000 abstract description 3
- 239000007787 solid Substances 0.000 abstract description 3
- 239000000443 aerosol Substances 0.000 abstract description 2
- 239000000428 dust Substances 0.000 abstract description 2
- 239000000839 emulsion Substances 0.000 abstract description 2
- 239000008187 granular material Substances 0.000 abstract description 2
- 238000002347 injection Methods 0.000 abstract description 2
- 239000007924 injection Substances 0.000 abstract description 2
- 239000000203 mixture Substances 0.000 abstract description 2
- 239000003921 oil Substances 0.000 abstract description 2
- 230000005068 transpiration Effects 0.000 abstract description 2
- 230000003129 miticidal effect Effects 0.000 abstract 2
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 abstract 1
- 230000003247 decreasing effect Effects 0.000 abstract 1
- 230000001747 exhibiting effect Effects 0.000 abstract 1
- 239000002316 fumigant Substances 0.000 abstract 1
- 239000007921 spray Substances 0.000 abstract 1
- 239000004563 wettable powder Substances 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-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
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-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
- 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 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
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 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
- 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
- 235000013312 flour Nutrition 0.000 description 2
- 238000000034 method Methods 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
- 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
- 101000958664 Homo sapiens Nucleus accumbens-associated protein 1 Proteins 0.000 description 1
- 101000631760 Homo sapiens Sodium channel protein type 1 subunit alpha Proteins 0.000 description 1
- 239000005909 Kieselgur Substances 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
- 102100028910 Sodium channel protein type 1 subunit alpha Human genes 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [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
- 241001454295 Tetranychidae Species 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 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
- 229960002903 benzyl benzoate Drugs 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004927 clay 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
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 1
- 229960001673 diethyltoluamide Drugs 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 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
- 238000003958 fumigation Methods 0.000 description 1
- 239000011521 glass 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
- 125000004435 hydrogen atom Chemical group [H]* 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
- 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
- 239000002904 solvent Substances 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
- 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
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NAC1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, propoxar NAC1 and others, phenyl salicylate, benzyl benzoate, 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、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、
1
1¥N −G OOR。(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 11\N-G OOR.
(ただし、R,、R,4i水素またはメチル基、R3は
炭素数1〜4のアルキル基)
で表される化合物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。(However, R,, R, 4i hydrogen or methyl group, R3 is an alkyl group having 1 to 4 carbon atoms) Compounds represented by these have excellent acaricidal effects and eliminate the drawbacks of conventional mite control agents. The present invention was completed based on the discovery that
すなわち本発明は、
R+
殉へ・C00島
(ただし、R,、R,は水素またはメチル基、R3は炭
素数1〜4のアルキル基)
で表される化合物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 as an active ingredient a compound represented by: It provides:
本発明の殺ダニ剤は、この R。The acaricide of the present invention R.
■ %−N −COOR。■ %-N -COOR.
(ただし、R,、R□は水素またはメチル基、R6は炭
素数1〜4のアルキル基)
で表される化合物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、噴震剤、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。(However, R,, R□ are hydrogen or a methyl group, and R6 is an alkyl group having 1 to 4 carbon atoms.) The compound represented by the above is combined and blended with a known liquid or solid carrier to form oils, emulsions, wettable powders, Fouling agent, aerosol agent,
It can be adjusted by preparing a suitable dosage form such as a powder, granule, fumigation agent, or 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, ethers such as tetrahydrofuran, dioxane, and dimethyl ether, hexane, kerosene, and n. Examples include aliphatic hydrocarbons such as paraffin and solvent naphtha, aromatic hydrocarbons such as benzene and toluene, 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
、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, wheat flour, and 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1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 an emulsifier, a dispersant, a spreading agent, a stabilizer, a propellant, and a volatilization regulator 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%重量此程ることが望まし
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. It is desirable that the amount is about 1 to 80% by weight, particularly 1 to 40% by weight.
なお、本発明の殺ダニ剤の有効成分である1 R,−N @G OOR。In addition, 1, which is an active ingredient of the acaricide of the present invention, R, -N @G OOR.
(ただし、R,、R,は水素またはメチル基、R1は炭
素数1〜4のアルキル基)
で表される化合物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7
散布させることが可能であり。(However, R,, R, is hydrogen or a methyl group, and R1 is an alkyl group having 1 to 4 carbon atoms.) Since the compound represented by these formulas volatilizes by itself and has acaricidal action, it should be sprayed on a large area of the room. The composition has a surface area suitable for
It is possible to disperse it.
便利である。こうすることにより、例えば骨中のダニに
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。It's convenient. By doing so, a sufficient effect can be expected against, for example, mites in bones, with fewer drug injection locations 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 R5 をN−GOOR。(Action and effect of invention) is the active ingredient of the acaricide of the present invention. R5 N-GOOR.
(ただし、RlRよは水素またはメチル基、R2は炭素
数1〜4のアルキル基)
で表される化合物は、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
有している。(However, RlR is hydrogen or a methyl group, and R2 is an alkyl group having 1 to 4 carbon atoms.) The compound represented by these formulas has an excellent action against Dermatophagoides mites, such as Dermatophagoides nigricans, and Dermatophagoides mites.
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、有効にダニ類
を駆除することができる。The acaricide of the present invention can be used indoors such as tatami mats, carpets, floors, hallways, bedding such as pine mattresses, futons, pillows, sofas, etc.
By applying it to furniture such as storage utensils, mites can be effectively exterminated.
特に、 をN−C0OR。especially, N-COOR.
(ただし、R,、Rユは水素またはメチル基、RJは炭
素数1〜4のアルキル基)
で表される化合物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。(However, R, and R are hydrogen or methyl groups, and RJ is an alkyl group having 1 to 4 carbon atoms.) Acaricides that utilize the self-volatilizing ability of compounds represented by the following can easily be used indoors in a short time. It is extremely advantageous because it can exterminate mites.
(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
ヤケヒヨウヒダニCDerrrrato ha oid
es 6μ!肛5sius)およびケナガコナダニ(江
筏吐組用匹江escentiae)を供試虫として用い
、下に示す揮散法で本発明の殺ダニ剤の効果を調べた。Example 1 Acaricidal test CDerrrrato haoid
es 6μ! The effectiveness of the acaricide of the present invention was investigated using the volatilization method shown below using the woolly mite (Escentiae escentiae) as the test insects.
この試験結果を第1表に示す。The test results are shown in Table 1.
メl友塾
内径1 am X高さ6aaのガラス製バイアルビンに
ケナガコナダニまたはヤケヒヨウヒダニを20〜〜30
匹入れ、バイアルビンの口を通気性テフロンフィルムで
覆った。一定量の供試試料を小ペトリ皿にとり、75%
飽和食塩水が入ったバイアルビンと共にIQのビーカー
内に入れた。ダニが入ったバイアルビンはフィルムで覆
った口を上にしてビーカー内に置いたわ
ビーカーの口を非通気性のフィルムで覆い、温度25℃
の環境下に24時間静置し、顕微鏡下で観察を行なった
。Melyujuku 20 to 30 woolen mites or brown spider mites are placed in a glass vial with an inner diameter of 1 am and a height of 6 aa.
The mouth of the vial was covered with a breathable Teflon film. Place a certain amount of the test sample in a small Petri dish, and
It was placed in the IQ beaker together with a vial containing saturated saline. The vial containing the mites was placed in a beaker with the film-covered mouth facing up.The beaker's mouth was covered with a non-porous film and the temperature was 25°C.
The sample was left standing for 24 hours under the following conditions and observed under a microscope.
(以下余白) 結果 第 1 表 −N、N−ジエチルー3−メチルベンザミド以上(Margin below) result Table 1 -N,N-diethyl-3-methylbenzamide or more
Claims (1)
3は炭素数1〜4のアルキル基)で表される化合物を有
効成分として含有する殺ダニ剤。[Claims] ▲There are mathematical formulas, chemical formulas, tables, etc.▼ (However, R_1 and R_2 are hydrogen or methyl groups, R_
3 is an acaricide containing a compound represented by C1-C4 alkyl group as an active ingredient.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5467190A JPH03258705A (en) | 1990-03-06 | 1990-03-06 | Miticide |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5467190A JPH03258705A (en) | 1990-03-06 | 1990-03-06 | Miticide |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03258705A true JPH03258705A (en) | 1991-11-19 |
Family
ID=12977244
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5467190A Pending JPH03258705A (en) | 1990-03-06 | 1990-03-06 | Miticide |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03258705A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100240693B1 (en) * | 1997-02-21 | 2000-03-02 | 마사토미 오츠카 | Airzole for mite disinfestation |
-
1990
- 1990-03-06 JP JP5467190A patent/JPH03258705A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100240693B1 (en) * | 1997-02-21 | 2000-03-02 | 마사토미 오츠카 | Airzole for mite disinfestation |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0233288B1 (en) | Acaricide | |
JP2017019875A (en) | Carbonyl containing compounds for controlling and repelling cimicidae populations | |
JPH03133903A (en) | Acaricide | |
JP2002356404A (en) | Mite controller | |
JPH03264504A (en) | Acaricide or mite repellent | |
CN104349672A (en) | Killing of bed bugs | |
JPH0539203A (en) | Composition for mite control | |
JP2609120B2 (en) | Acaricide for airless mites containing a quaternary ammonium salt as an active ingredient | |
JPH0459703A (en) | Miticide | |
JPH03258705A (en) | Miticide | |
JP2897054B2 (en) | Acaricide | |
JPS6059881B2 (en) | Wool pest repellent | |
JP2924102B2 (en) | Acaricide | |
KR20060110655A (en) | Chemical compound having acaricidal activity | |
KR100472643B1 (en) | Composition comprising plant oil and chemical compound having acaricidal activity | |
JP3465854B2 (en) | Indoor dust mites | |
JP3085681B2 (en) | Acaricide | |
JPS5839604A (en) | Agent for suppressing ingestion damage of wool vermin | |
JPH03106805A (en) | Acaricide | |
JPS60239402A (en) | Miticidal agent | |
JP2572994B2 (en) | Acaricide containing dimethylalkyl betaine as an active ingredient | |
JP2605779B2 (en) | Acaricide | |
JPH02142708A (en) | Indoor dust and stabilization thereof | |
JPH05170601A (en) | Insect-proofing agent | |
JPH0517312A (en) | Insecticidal, moth-proofing and vermin-repelling agent containing carboxylic acid ester derivative and volatile at normal temperature, and insecticidal, moth-proofing and vermin-repelling method using the same |