JPS6042314A - Mite-controlling composition - Google Patents
Mite-controlling compositionInfo
- Publication number
- JPS6042314A JPS6042314A JP58152058A JP15205883A JPS6042314A JP S6042314 A JPS6042314 A JP S6042314A JP 58152058 A JP58152058 A JP 58152058A JP 15205883 A JP15205883 A JP 15205883A JP S6042314 A JPS6042314 A JP S6042314A
- Authority
- JP
- Japan
- Prior art keywords
- mite
- mites
- resmethrin
- composition
- present
- 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
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- 229940108410 resmethrin Drugs 0.000 claims abstract description 14
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- 238000009423 ventilation Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
Abstract
Description
【発明の詳細な説明】 本発明はダニ防除組成物(・こ関する。[Detailed description of the invention] The present invention relates to a mite control composition.
槌来から屋内11のダニて、人間に対して重要な岐害を
もたらすものにイエダニ(Or旧tl+onyssus
bacoLi ) かよく知られていた。しかし近年性
や家屋1夷から発生ずるコナダニ類やチリダニ類(ヒヨ
ウヒダニ!ljr ) ”L tr−これらを捕食する
ツメダニ類ノアレルギー、虫咬Jiなどが問題となり、
これらのダニB’ilの防除に従来から害虫類の防除に
使用されていた41機リン殺虫剤、カーバフ−1−系殺
虫剤、ピレスロイド系殺虫剤などが試みられているか、
いずれも防除め決手にはならず、安全性の1mからピレ
スロイド系殺虫剤の前片が多くな−〕でいる。Among the 11 indoor mites from Tsuchiki, dust mites (or former tl+onyssus) are among the ones that cause important harm to humans.
bacoLi) was well known. However, in recent years, allergy and insect bites have become a problem due to the presence of dust mites and dust mites that prey on these mites.
Have any attempts been made to control these mites B'il, such as 41-phosphorus insecticides, Carbuff-1-based insecticides, and pyrethroid insecticides, which have traditionally been used to control pests?
None of these methods are decisive for controlling insect pests, and many use pyrethroid insecticides from a safe distance of 1 m.
コノヒレスロイド糸殺虫剤の中でもレスメスリンの殺ダ
ニ効果が優れていることか最近わかってきた。しかしな
がら、ヒヨウヒダニとコナダニのレスメスリン感受性を
調べてみると、コナダニはレスメスリンに対する感受性
が低く、このためコナダニtこ対し有効な有機リン剤と
の01用か試みられたこともあるか、効果が不十分であ
り、安全性にも疑問かあった。このようなことから、特
に屋内塵中Qこ生息するヒヨウヒダニtこ対しては低濃
度レスメスリン処理で十分な殺ダニ効果か得られるが、
竹の中や食品から発生するコナダニに対してはレスメス
リン処理では十分といえないため筒金的な屋内での殺ダ
ニ剤が切望されているのか現状である。It has recently been discovered that resmethrin has an excellent acaricidal effect among the Konohilethroid insecticides. However, when examining the susceptibility of Dermatophagus mites and Dermatophagus mites to resmethrin, it was found that mites are less sensitive to resmethrin.For this reason, attempts have been made to use organic phosphorus agents that are effective against mites, but the effect is insufficient. There were also questions about safety. For these reasons, low-concentration resmethrin treatment is sufficient to kill mites, especially against Dermatophagoides mites that live in indoor dust.
Since resmethrin treatment is not sufficient to kill mites that occur inside bamboo or on food, there is a strong need for a miticide that can be used indoors.
本発明者らは、上記現状に鑑み優れた殺ダニ剤を桿供す
ることを目的とし、屋内のダニに苅してイq幼てかつ安
全性の高い殺ダニ剤の検討を試みた結果、レスメスリン
(異性体を含む)と食品にも使用されている安息香酸ベ
ンジルを組合せることtこより、ダニtこ苅してさらに
有効な殺ダニ効果を見出し本発明を完成した。In view of the above-mentioned current situation, the present inventors aimed to provide an excellent acaricide, and as a result of trying to find a highly safe acaricide that can be applied to indoor ticks to keep them young, the inventors found that resmethrin By combining benzyl benzoate (including isomers) and benzyl benzoate, which is also used in foods, we found a more effective mite killing effect and completed the present invention.
すなわち本発明はレスメスリン(異性体を含む)と安息
香酸ペンシルとを自〃ノ成分として含有することを特徴
とするダニ防除組成物tこ保る。That is, the present invention provides a mite control composition containing resmethrin (including isomers) and benzoic acid pencil as its own ingredients.
本発明の殺ダニ組成物はその有効成分として、レスメス
リン(異1コL体?含む)と安1口、1酸ペンシルとを
含有することに占(づいて、極めて優れた相乗効果を奏
しつる。The acaricidal composition of the present invention contains, as its active ingredients, resmethrin (including the hetero-1-L form) and 1-acid pencil, and therefore has an extremely excellent synergistic effect. .
本発明の殺ダニ効果は、ツツガムシ、ヒヨウヒダニ、コ
ナダニ、ヒセンダニ、ニキビダニ、イエダニ、ワクモ、
トリ→)−シダニ、ツメダニ、シラミダニ、ハリクチダ
ニ、ホコリダニ、ササラダニ、ニクダニに対し強力なも
のである。The acaricidal effect of the present invention can be applied to chiggers, house dust mites, mites, Demodex mites, house dust mites, red mites, red mites,
Bird→) - It is strong against wood mites, claw mites, lice mites, leaf mites, dust mites, sand mites, and black mites.
従って本発明のダニ防除剤はこれを家庭内のクタミ、カ
ーペノ+−等や食物収納庫及び人体、動物体、植物体t
こ適用することeこよって、之等の場所で棲息又寄生し
ている種々のダニに対して確実な殺ダニ効果を発揮し、
ひいては、動物体のダニによる刺咬、吸血、アレルギー
性疾患をも的確に回避できるものである◇
本発明において、有効成分の配合割合はレスメスリン1
に対し安息香酸ベンジル05以」二、好ましくはレスメ
スリンlに対し安息香酸ベンジJv1す」二を自己合す
るのがよい。Therefore, the mite control agent of the present invention is effective against mites, carpeno+-, etc. in the home, food storage areas, human bodies, animals, plants, etc.
By applying this, it exhibits a reliable acaricidal effect against various mites living or parasitic in these places,
Furthermore, it is possible to accurately avoid tick bites, blood sucking, and allergic diseases in animals.◇ In the present invention, the blending ratio of the active ingredients is 1:
It is preferable to self-combine benzyl benzoate Jv1 to resmethrin I.
本発明のダニ防除組成物は、上記組成物をそのままダニ
防除を要求される区域等に適用することもできるが、通
常好ましくは適当な担体その飴の配合剤を用いて適用区
域、適用方法等eこ適した各種の形暢例えば液剤、固剤
等Pこ調製して利用される。液剤の形態tこ調製するに
当り用いられる担体としては例えは水、メチルアルコー
ル、エチIレアルコール等のアルコール類、アセトン、
メチルエチルIf )ン等のケトン類、テ1ラヒドロフ
ラン、シオキ勺ン等のエーテ/I/頬、ヘギサン、ケロ
シン、パラフィン、45曲ベンジン等の脂肪族炭化水素
類、ベンセン、トルエン等の芳香族炭化水素4」1、酢
酸エチル等のエステルm 、ジクロIJエタン等のハロ
ゲン化がぜ化水素43゛1等を例示できる。之等液剤の
形■の本発明ダニ防除剤には更をこ通常のケ漢形成剤、
乳化刑、分散イリ、展着剤、iM flVI nυ、安
定剤、Iす′1月、1イリ等の添加削を配合することが
てぎ、倹料形態、接沼刑形惨、乳削、分散剤、だl蜀剤
、ローンヨン、クリ−・ム、噴霧剤、エアゾール剤等の
形態で利用することかてきる。之等の添加斉0としては
、例えは二10セルローヌ、アセチルセlレローヌ、ア
セチルブチリルセルロース、メチルセルロース等のセル
ロース誘導体、酢酸ビニル樹脂等のビニル系位+++旨
、アノレキノド系樹1(旨、ユリア糸樹1(旨、エボ″
キシ井切脂、ポリエステル系樹脂、ウレターン系向脂、
シリコン系樹脂、アクリル平(61脂、塩化ゴム、ポリ
ビニルアルコール等の塗膜形成剤、石けん類、ポリオキ
シエチレンオレイルエーテルなどのポリオキシエチレン
J脂肪アルコールエーテル、ポリオキシエチレンノニル
フェニルエーテルナトのポリオキシエチレンアルキルア
リルエーテル、ポリオギンエチレン脂肪酸エステル、脂
ljh酸りリセリド、ソルビクン脂肪酸エステル、高級
アルコールの硫酸エステル、rデンルベンゼンスルホン
酸ソーダなどのアルギルアリルスルホン酸塩等の界面活
性nlJ 、 ((1,化石?ll+ガス、ジメチルエ
ーテル、フルオロカーボン等の噴射剤、カゼイン、ゼラ
チン、アルギン酸、CMC等を例示できる。The mite control composition of the present invention can be applied as it is to areas where mite control is required, but it is usually preferable to use a suitable carrier, candy formulation, etc. to apply the area, application method, etc. It can be prepared and used in various suitable forms, such as liquid preparations and solid preparations. Examples of carriers used in preparing the liquid formulation include water, alcohols such as methyl alcohol and ethyl alcohol, acetone,
Ketones such as methyl ethyl if), esters such as tetrahydrofuran, esters, aliphatic hydrocarbons such as paraffin, kerosene, paraffin, benzine, aromatic carbons such as benzene, toluene, etc. Examples include hydrogen 4'1, esters such as ethyl acetate, and halogenated hydrogen oxides such as dichloroIJ ethane. The liquid form of the tick control agent of the present invention further contains a conventional tick-forming agent,
Additives such as emulsification, dispersion, spreading agent, iM flVI nυ, stabilizer, ISU'1, 1, etc. can be added to the formulation, emulsification, emulsification, emulsion, milking, etc. It can be used in the form of a dispersant, a balm, a lotion, a cream, a spray, an aerosol, and the like. Examples of additives include cellulose derivatives such as 210 cellulone, acetyl cellulose, acetyl butyryl cellulose, and methyl cellulose, vinyl-based +++ compounds such as vinyl acetate resin, anolequinodo-based trees 1, and urea fibers. Tree 1 (effect, evo''
Kishiikiri fat, polyester resin, urethane resin,
Silicone resins, acrylic flats (61 fats, chlorinated rubber, coating film forming agents such as polyvinyl alcohol, soaps, polyoxyethylene J fatty alcohol ethers such as polyoxyethylene oleyl ether, polyoxyethylene such as polyoxyethylene nonyl phenyl ether) Surfactants such as ethylene alkyl allyl ether, polyogine ethylene fatty acid ester, fat ljh acid lyceride, sorbicun fatty acid ester, sulfuric acid ester of higher alcohol, argylyl allyl sulfonate such as sodium benzene sulfonate, etc. 1. Fossil gas, dimethyl ether, propellants such as fluorocarbon, casein, gelatin, alginic acid, CMC, etc. can be exemplified.
また固剤の形態に調製するに当り用いられる担体として
は、例えばケイ酸、カオリ、ン、活性炭、ベントナイト
、珪藻土、タルク、クレー、伏酸カルシウム、陶磁器粉
等の鉱物質粉末や、木粉、大豆粉、小麦粉、でん粉等の
植物質粉末等やシクロデキストリン等の包接化合物等を
例示できる。更に該開削の形態に調製するに当っては、
例えばトリシクロテ゛カン、シクロトチ゛カン、2.4
.6−1−リイソプロビルー1.3.5−トリオキサン
、トリメチレンノルホル不ン等の列1自性担体やパラジ
クロロベンゼン、ナフタリン、樟脳等の+1范性防虫剤
を用い、上記組成物を溶融混合又は拮請混合後成型して
、別画性固剤とすることもQ¥る。In addition, examples of carriers used in preparing a solid form include mineral powders such as silicic acid, kaolin, activated carbon, bentonite, diatomaceous earth, talc, clay, calcium oxate, and ceramic powder; wood powder; Examples include vegetable powders such as soybean flour, wheat flour, and starch, and clathrate compounds such as cyclodextrin. Furthermore, in preparing the cut-and-cut form,
For example, tricyclotecan, cyclotothican, 2.4
.. 6-1-liisoprobyl-1.3.5-trioxane, trimethylenenorformane, etc., and a +1 insect repellent such as paradichlorobenzene, naphthalene, camphor, etc., are used to melt-mix or melt-mix the above composition. It is also possible to mold the mixture after mixing to form a separate solid agent.
また上記固カリには、組成物をプラスチックスに練り込
/した樹脂成型物の形郭も包含される。The above-mentioned hard potash also includes the shape of a resin molded product obtained by kneading the composition into plastics.
史には、カーペノ1−のバッキング剤にt足台すること
も可能である。Additionally, it is also possible to use a backing agent of Carpeno 1.
また本発明のダニ防除組成物は、例えばポリビニルアル
コールや(: M C等を用いたスプレードライ法、ゼ
ラチン、ポリビニルアルコール、アルギン酸等を用いた
液中硬化法、コアセルベーンカン法等に従いマイクロカ
プセル化した形Btこ調製しタリ、ベンジリデン−D−
ソルビトール、カラギーナン等のゲル化剤を用いてゲル
の形態tこ調製することもできる。In addition, the mite control composition of the present invention can be prepared into microcapsules according to, for example, a spray drying method using polyvinyl alcohol or MC, an in-liquid curing method using gelatin, polyvinyl alcohol, alginic acid, etc., a core cell benecan method, etc. The converted form Bt was prepared from benzylidene-D-
Gel forms can also be prepared using gelling agents such as sorbitol and carrageenan.
更に本発明のダニ防除組成物tこは、公知の害虫忌避剤
、効力増強剤、酸化防止剤、殺虫剤、げっ歯動物駆除及
び忌避剤、殺菌剤、防徴剤、除草剤、肥料、着香犯、5
a色料等を配合することができる。Furthermore, the mite control composition of the present invention may contain known pest repellents, potency enhancers, antioxidants, insecticides, rodent control and repellents, fungicides, repellents, herbicides, fertilizers, and pesticides. Incense criminal, 5
(a) A colorant etc. can be blended.
配合可能な他の害虫忌避剤としては、N、N−ジエチル
−メタ−トルアミド、2.3.4.5−ビス(Δ2−プ
チレン)−テトラヒドロフlレフラール、ジ−n−プロ
ピル、イソシンコメロネート、ジ−n−1チルサクシネ
ート、2−ヒドロキシエチルオクチルサルファイド等を
、効力増強剤としてはN−(2−エチルヘキシル)−ビ
シクロ−(2,2,1)−5−へ1テン−2,3−ジカ
ルボキシイミド、6−(プロピルビペロニル)−プチル
ヵルビチルエ−? ル等ヲ、酸化防止剤としてはブチル
ヒドロキシアニソール、ジブチルヒドロキシトルエン、
トコフェロール、r−オリザノール等を、殺虫Mとして
は一般名アレヌリン及びその幾何及び(又は)光学異性
体等のピレノロイド類を、げっ歯動物駆除及び忌Jw剤
としてはα−ナフチルチAウレア、シクロベキシミ1゛
等ヲ、殺沼剤としてはサリチル酸、p−クロロ−2ノl
−キシレノール、2− (4’−チアゾイル)″ベンズ
イミダゾール等を、防願剤としてはα−10モ7ンナミ
ノクアルデヒド、N−ジメチル−N−フェニル+N’−
(フルオロジクロロメチIし)チオスルファミド等を夫
々例示できるか、これらに限定されるものではない。Other pest repellents that can be blended include N,N-diethyl-meta-toluamide, 2.3.4.5-bis(Δ2-butylene)-tetrahydrofurfural, di-n-propyl, and isocincomero. N-(2-ethylhexyl)-bicyclo-(2,2,1)-5-1ten-2,3 as a potency enhancer. -dicarboximide, 6-(propylbiperonyl)-butylcarbityl ether? Examples of antioxidants include butylhydroxyanisole, dibutylhydroxytoluene,
Tocopherol, r-oryzanol, etc. are used as insecticides, pyrenoloids such as the common name arenuline and its geometric and/or optical isomers are used as insecticides, and α-naphthylthiA urea and cyclobeximi 1 are used as rodent exterminators and repellents. etc., as a swamp killer, salicylic acid, p-chloro-2nol
-xylenol, 2-(4'-thiazoyl)''benzimidazole, etc., and anti-application agents such as α-10monaminoqualdehyde, N-dimethyl-N-phenyl + N'-
Examples include (fluorodichloromethane), thiosulfamide, etc., but are not limited to these.
カベして:A製される各種形態を有する本発明のダニ防
除組成物は、その使用に当り防除効果を要求されるダニ
の棲息区域例えば一般家庭、穀物倉庫、食堂の厨m、家
具、押入れ、玄関、洗1m所等に載置、撒布、噴霧、塗
布、貼り付は等により、また動物体自体に撒竹J、噴霧
、塗布等により適用できる。The mite control composition of the present invention, which has various forms made of:A, is suitable for use in areas where mites live, such as general households, grain warehouses, cafeterias, furniture, and closets where a mite control effect is required. It can be applied by placing, scattering, spraying, applying, pasting, etc. on the entrance, washing area, etc., or by spraying, applying, etc. to the animal body itself.
また本発明のダニ防除組成物は、これを予め適当なシー
ト状基材に塗布、含浸、滴下、混練等により保持きせて
、該基拐に保持された形態で目的とする箇所に載置した
り貼り合ぜることにより利用することもできる。この1
祭用いられるシート伏基イ2としては、例えばポリエチ
レン、ポリプロピレン、ナイロン、ホリ塩化ビニル、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lR維棒体シート紙、布、不織布、
皮革等)、2等合成1司脂と無機質繊維または粉体との
混合シートまたは混紡布、上記合成(至)脂と動(直物
繊糸11との混紡布または不撒布、アルミニウム、ステ
ンレス、411鉛等の金属の箔乃至フィルム及び」二記
各種シー1の積層シートを例示できる。Furthermore, the mite control composition of the present invention can be applied to a suitable sheet-like base material in advance by applying it, impregnating it, dropping it, kneading it, etc., and then placing it on the desired location in a form that is retained on the base material. It can also be used by pasting together. This one
Examples of sheet materials used in festivals include synthetic resin sheets such as polyethylene, polypropylene, nylon, polyvinyl chloride, polyvinylidene chloride, and polyester;
Animal/plant material or inorganic 1R fibrous sheet paper, cloth, non-woven fabric,
(leather, etc.), mixed sheets or blended fabrics of 2nd grade synthetic 1st fat and inorganic fibers or powder, blended fabrics or non-spread fabrics of the above synthetic fats and dynamic (straight yarn 11), aluminum, stainless steel, Examples include foils or films of metals such as 411 lead and laminated sheets of various types of sheets 1 described in 2.
本発明ダニ防除組成物中の有効成分混合物量及び該防除
組成物の適用量(ま、その剤型や適用方法、適用場所等
に応じて心室に法定ずれはよく、限定的ではないか、〕
m常分散f:lJや水和剤等の散剤の形rルで用いる場
合、有効成分混合物を1〜80重量%〃fましくは5〜
40重基%含有させればよく、粉剤等の固バυの形態と
する場合1〜50重量%好ましくは2〜2υ重JA%含
有させれはよく、またソート状基拐や穎具部A!シこ保
持させた形態とする場合には、基H等の飽和召I(爪の
ほぼ局倍量を保持させればよい。また本発明ダニ防除組
成物の適用量としては、例えば塗布使用の場合、塗布す
べぎ面ft!t l y)i当り有効成分混合物として
0005り〜xy、好*しくはレヌノヌリン0.01
g〜017、安息香酸ペンシル0.005 g〜0.3
gとするのが殺ダニ効果、又薬剤の刺激性からみてよ
い。The amount of the active ingredient mixture in the mite control composition of the present invention and the amount applied of the control composition (well, depending on the dosage form, application method, application location, etc., the legal deviation in the ventricle is good, but is not limited?)
m Normal dispersion f: When used in powder form such as lJ or wettable powders, the active ingredient mixture is 1 to 80% by weight, preferably 5 to 80% by weight.
It is sufficient that the content is 40% by weight, and when it is in the form of a solid bar such as a powder, it may be contained by 1 to 50% by weight, preferably 2 to 2% by weight. ! When the mite-controlling composition of the present invention is kept in a form in which the mite-controlling composition of the present invention is applied, for example, the amount of the saturated compound I such as H (approximately double the amount of nails) may be maintained. 0005~xy as the active ingredient mixture per application surface ft!tly y)i, preferably renunonulin 0.01
g~017, benzoic acid pencil 0.005 g~0.3
From the viewpoint of the acaricidal effect and the irritant nature of the drug, it is appropriate to set it to 1.g.
固剤その他の形態で用いる場合、適用空間177.1’
当り有効成分化合物を約 /1 以上存在さぜるのか適
当である。When used as a solid or other form, the application space 177.1'
It is appropriate for the active ingredient compound to be present in an amount of about 1:1 or more.
以下に本発明ダニ防除組成物を実施例、試験例にもとず
き詳卸)eこ説明する。The mite control composition of the present invention will be explained in detail below based on Examples and Test Examples.
実施例ル
スメスリン及び安息香酸ペンシルの所定是をアセトンに
浴解し、下記の表に示したようにそれぞれグラフ1紙(
5(7)x 5 cm )に処理し、風乾してアセトン
を除去し、それぞれのノート形態の木兄Iす1ダニ防除
組成物を得た。Examples Predetermined amounts of lusmethrin and benzoic acid pencil were dissolved in acetone, and one graph paper (each) was prepared as shown in the table below.
5 (7) x 5 cm) and air-dried to remove acetone to obtain each notebook-shaped mite control composition.
1 0、01 0.001
2 0、01 0.005
3 0、01. 0.01
4 0、01 0.03
5 Q、 OL 0.05
試験例1
実砲例1で示したクラフト紙に、同様の操作テレヌメヌ
リン単独、安7山、香酸ペンシル単独を処理し、これら
をりj照として試験した。1 0,01 0.001 2 0,01 0.005 3 0,01. 0.01 4 0,01 0.03 5 Q, OL 0.05 Test Example 1 The kraft paper shown in Actual Artillery Example 1 was treated with terenumenulin alone, Yasuyama, and fragrant pencil alone in the same manner. was tested as a reference.
処理グラフl−紙をポリ袋に入れ、この中に約4005
flのダニ、ケナガコナダニ又はコナヒヨウヒダニを別
4に投入し密封した。24時間後(コナヒヨウヒダニの
場合は72時間後も観禁)、ポリ袋の中のダニの生死を
顕徽境下でvh 11 L、致死率を≧くめた。なお、
数1直はずへてブランクの致死率からアボットi’+l
i正して算出した。Processing graph l - Put the paper in a plastic bag and put about 4,005 yen in it.
fl mites, woolly mites, or phyllotid mites were placed in a separate container 4 and sealed. After 24 hours (in the case of Dermatophagoides mites, observation was not allowed even after 72 hours), the mites in the plastic bag were checked for life and death under conditions of vh 11 L, and the mortality rate was ≧. In addition,
Abbot i'+l from the blank fatality rate
Calculated by correcting i.
その結果、−1:表にボずように実砲例1て得た本発明
ダニ防除組成物は、明らかに4’12乗効果がR4イさ
れた。As a result, -1: As shown in the table, the tick control composition of the present invention obtained in Actual Example 1 clearly had a 4'12 power R4 effect.
実施例2
レフフッ9フ01部と安腟、香酸ペンシル0.28Bと
の混合物をアセトン20部に溶解し、300ノノンユク
レ一997部を加え十分Qこ攪拌した後、アセトンを留
去して本発明ダニ防除組成物の。3%粉剤を得た。Example 2 A mixture of 01 parts of Leffu 9F and 0.28B of Anvaginal Fragrance Pencil was dissolved in 20 parts of acetone, 997 parts of 300 Nonon Yukre was added and stirred thoroughly, and the acetone was distilled off. Inventive mite control composition. A 3% powder was obtained.
実施例3
レスメスリン25部と安息香酸ベンジル75部との混合
物10部Qこツルポール3005(東邦化学■1)何品
名)15部、キジロール75部を加え、これらをよく攪
拌混合溶解し、本発明ダニ防除組成物の10%乳剤を得
た。Example 3 10 parts of a mixture of 25 parts of resmethrin and 75 parts of benzyl benzoate were added, 15 parts of Q Kotsurpol 3005 (Toho Chemical ■1) (product name), and 75 parts of Kijirol were mixed and dissolved by stirring well. A 10% emulsion of the pesticidal composition was obtained.
実す亀例4
レフフッ921部と安息香酸ペンシル1部の混合物やこ
リダニンスルホン酸ソーダ(結合剤)2部を加え、クレ
ー(増量剤)96部を加え、攪拌器中にて十分攪拌混合
する。Example 4: Add a mixture of 921 parts of Refufu and 1 part of benzoic acid pencil, 2 parts of sodium pyridanine sulfonate (binder), add 96 parts of clay (filler), and stir and mix thoroughly in a stirrer. .
ついて水をこれら混合物のlO%量加えさらに攪拌混合
して迄粒機にまって製粒し、通風乾燥して、本発明ダニ
防除組成物の2%粒剤を得た。Then, water was added in an amount of 10% of these mixtures, and the mixture was further stirred and mixed, and the mixture was granulated in a granulator, followed by ventilation drying to obtain 2% granules of the mite control composition of the present invention.
実施例5
レスメスリン0.1部、安息香酸ベンジル03部、キン
ロール7部、脱臭灯油76部を混合溶解する。Example 5 0.1 part of resmethrin, 03 parts of benzyl benzoate, 7 parts of Kinrole, and 76 parts of deodorized kerosene are mixed and dissolved.
これをエアゾール容8Kに充填し、バルブ部分を取(′
:1けた後、該バIレプ部分を通じて液化石油ガス85
部を加圧充填して本発明ダニ防除組成物のエアゾール剤
を得た。Fill this into an aerosol volume of 8K and remove the valve part ('
: After 1 digit, liquefied petroleum gas 85
An aerosol preparation of the mite control composition of the present invention was obtained by filling the sample under pressure.
実殉例6
レフフッ9フ02部と安息香酸ベンジル0.3 flf
liの混合物を白灯油に溶解し、全体を100部として
本発明ダニ防除組成物の04%油剤を得る。Actual case 6 9 flf 02 parts and 0.3 flf benzyl benzoate
The mixture of li is dissolved in white kerosene and the total amount is 100 parts to obtain a 4% oil solution of the mite control composition of the present invention.
実施例7
実施例5に示した油剤5g及び効力増強剤としてN−(
2−エチルヘキシル)−ヒシクC1−C2゜2、1 )
−5−へブテン−2,3−7カルボキシイミド5gを
11−ヘキサン11に希釈混合し、不織布〔ポリエチレ
ン−木綿(3:1重量比)製、厚さ300μ、面積11
ノ2’ )に、該混合物が30gとなるように含浸後乾
燥して、シート状形態の本発明ダニ防除組成物を得た。Example 7 5 g of the oil shown in Example 5 and N-(
2-Ethylhexyl)-Hisik C1-C2゜2,1)
- 5 g of 5-hebutene-2,3-7 carboximide was diluted and mixed with 11-hexane, and a non-woven fabric [made of polyethylene-cotton (3:1 weight ratio), thickness 300μ, area 11
2'), the mixture was impregnated to a weight of 30 g and dried to obtain a sheet-shaped mite control composition of the present invention.
(以上) 特r1出願人 アース製薬株式会社 75(that's all) Special r1 applicant Earth Pharmaceutical Co., Ltd. 75
Claims (1)
イ]幼成分として含有することを特徴とするダニ防除組
成物。A mite control composition comprising resmethrin (including isomers) and benzoic acid pencil as juvenile components.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58152058A JPS6042314A (en) | 1983-08-19 | 1983-08-19 | Mite-controlling composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58152058A JPS6042314A (en) | 1983-08-19 | 1983-08-19 | Mite-controlling composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6042314A true JPS6042314A (en) | 1985-03-06 |
JPH0363527B2 JPH0363527B2 (en) | 1991-10-01 |
Family
ID=15532127
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58152058A Granted JPS6042314A (en) | 1983-08-19 | 1983-08-19 | Mite-controlling composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6042314A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0331206A (en) * | 1989-06-28 | 1991-02-12 | Fumakilla Ltd | Acaricide composition |
WO1998036640A1 (en) * | 1997-02-20 | 1998-08-27 | Reckitt & Colman Inc. | Dust mite control compositions containing benzyl benzoate and alcohol |
WO1999007220A1 (en) * | 1997-08-06 | 1999-02-18 | Reckitt & Colman Inc. | Compositions for controlling dust mites and their allergens |
US6107341A (en) * | 1997-12-19 | 2000-08-22 | Bissell Homecare, Inc. | Aqueous miticide containing benzyl benzoate |
EP1104233A4 (en) * | 1998-05-18 | 2001-08-22 | West Agro Inc | Improved film-forming compositions for protecting animal skin |
US6376542B1 (en) * | 1997-12-19 | 2002-04-23 | Bissell Homecare, Inc. | Aqueous miticide compositions containing benzyl benzoate |
ITMI20081372A1 (en) * | 2008-07-25 | 2010-01-26 | Synthesis Srl | SANITIZING PRODUCT FOR THE TREATMENT OF PUBLIC USE SEATS |
CN114886884A (en) * | 2022-05-07 | 2022-08-12 | 深圳市精联华科技有限公司 | Emulsion containing 25% benzyl benzoate and used for removing skin mites |
-
1983
- 1983-08-19 JP JP58152058A patent/JPS6042314A/en active Granted
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0331206A (en) * | 1989-06-28 | 1991-02-12 | Fumakilla Ltd | Acaricide composition |
WO1998036640A1 (en) * | 1997-02-20 | 1998-08-27 | Reckitt & Colman Inc. | Dust mite control compositions containing benzyl benzoate and alcohol |
US5916917A (en) * | 1997-02-20 | 1999-06-29 | Reckitt & Colman Inc. | Dust mite control compositions containing benzyl benzoate and alcohol |
WO1999007220A1 (en) * | 1997-08-06 | 1999-02-18 | Reckitt & Colman Inc. | Compositions for controlling dust mites and their allergens |
US6107341A (en) * | 1997-12-19 | 2000-08-22 | Bissell Homecare, Inc. | Aqueous miticide containing benzyl benzoate |
US6376542B1 (en) * | 1997-12-19 | 2002-04-23 | Bissell Homecare, Inc. | Aqueous miticide compositions containing benzyl benzoate |
EP1104233A4 (en) * | 1998-05-18 | 2001-08-22 | West Agro Inc | Improved film-forming compositions for protecting animal skin |
ITMI20081372A1 (en) * | 2008-07-25 | 2010-01-26 | Synthesis Srl | SANITIZING PRODUCT FOR THE TREATMENT OF PUBLIC USE SEATS |
CN114886884A (en) * | 2022-05-07 | 2022-08-12 | 深圳市精联华科技有限公司 | Emulsion containing 25% benzyl benzoate and used for removing skin mites |
Also Published As
Publication number | Publication date |
---|---|
JPH0363527B2 (en) | 1991-10-01 |
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