JPS61291507A - Rodent repellent - Google Patents

Rodent repellent

Info

Publication number
JPS61291507A
JPS61291507A JP60135087A JP13508785A JPS61291507A JP S61291507 A JPS61291507 A JP S61291507A JP 60135087 A JP60135087 A JP 60135087A JP 13508785 A JP13508785 A JP 13508785A JP S61291507 A JPS61291507 A JP S61291507A
Authority
JP
Japan
Prior art keywords
liquid
rodent
ethanol
acid
ethyl acetate
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
Application number
JP60135087A
Other languages
Japanese (ja)
Other versions
JPS6332327B2 (en
Inventor
Toshio Yamada
山田 俊雄
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
HAKUYO KOSAN KK
Original Assignee
HAKUYO KOSAN KK
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by HAKUYO KOSAN KK filed Critical HAKUYO KOSAN KK
Priority to JP60135087A priority Critical patent/JPS61291507A/en
Publication of JPS61291507A publication Critical patent/JPS61291507A/en
Publication of JPS6332327B2 publication Critical patent/JPS6332327B2/ja
Granted legal-status Critical Current

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Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE:To obtain the titled agent effective to give a rodent with disagreeable feeling and repel the rodent without killing by using shikimic acid, etc., as a main component, mixing the component with ethyl acetate, etc., used as subsidiary component and a mustard glycoside having catalytic action, aging the mixture, separating into solid and liquid, and adding HANSHO liquid, formalin, etc., to the liquid extract. CONSTITUTION:Shikimic acid, toxin, amino acid and KUJIN (root of Sophora angustifolia) alkaloid are used as the main components, mixed with subsidiary components composed of water, ethanol, acetic acid and ethyl acetate and with mustard glucoside acting as a catalyst, and the mixture is aged. After aging, the mixture is separated into solid and liquid e.g. by centrifugal separator, etc., and the liquid component is collected. The extracted liquid is mixed with HANSHO liquid, SHIKIMI (Illicium anisatum L.) liquid, chrysanthemum liquid, raw starfish liquid, formalin, pyridine and ethanol. The activity can be further improved by the addition of orange oil. Rodent is attracted by the evaporated active components such as ethyl acetate, formalin, etc., and the nerve is unbalanced by the absorption of the main components such as shikimic acid, etc., to make the rodent dislike the odor.

Description

【発明の詳細な説明】 (イ) 産業上の利用分野 本発明は、ねずみが嫌畏する薬剤に関するものである。[Detailed description of the invention] (b) Industrial application field The present invention relates to a drug that is feared by mice.

(ロ) 従来の技術 従来、ねずみは、繁殖力がとても強くて年に数回子ども
を産み、駆除の手をゆるめるとたちまち一面にはびこる
ようになり、際限なく被害を及ぼしている。
(b) Conventional technology Conventionally, rats have a very strong reproductive capacity and give birth to children several times a year, and if we slack off on exterminating them, they quickly infest the area, causing endless damage.

例えば、ねずみは我々の主食である米麦を好んで食する
ことより、台所や穀倉における被害は厖大なものであり
、また、畑では芋をかじり野菜をあらし、ときには養鶏
場のひなを一夜のうちに皆殺しにすることがあり、また
、森林地帯に住む野ねずみは、腹のすいていないときで
も何かをかじっていないと、門歯が伸びすぎて摩耗障害
をおこすものであり、そのために鉛管までも食いやぶっ
てガスを漏らせたり、電灯線をかみやぶって針金を露出
させ、火事の原因をひきおこすとさえあり、この種のね
ずみによる損害は厖大なものとなっている。
For example, rats prefer to eat rice and wheat, which is our staple food, and they cause enormous damage to kitchens and granaries.They also gnaw potatoes and destroy vegetables in the fields, and sometimes destroy chicks in poultry farms overnight. In addition, if field mice living in forest areas do not gnaw on something even when they are not hungry, their incisors will grow too long and cause wear problems. These rats can cause a tremendous amount of damage, causing gas to leak by chewing through them, or by chewing over power lines, exposing wires and even causing fires.

そこで、上記のようなねずみ被害を防除すべく多種多様
の殺鼠剤が開発されており、同殺鼠剤は、主としてねず
みの好むえさに混入して、いわゆる毒えさを作って通路
や穴に置き、これを食べさせることによって中毒死させ
るものである。かかる殺鼠剤として従来用いられた化合
物には、黄リン、亜と酸、タリウム、バリウム等の無機
塩類等の他、ストリキニーネ等の有機化合物、及び植物
性のものとしてレッドスキル等があり、野ねずみの防除
には明治の末年から野ねずみチフス菌が用いられてきた
が、衛生上の見地から昭和23年にその使用が禁止され
た。そして、第二次大戦後は、アンツー、モノフルオロ
酢酸ナトリウム、ワルハリン、カストリックス、ムリタ
ン等の有機合成殺鼠剤があいついで実用に移され、ねず
みの科学的防除に多きな発展をもたらした。なかでも、
ワルハリンのようなりマリン系化合物は、その抗凝結性
を利用し、ねずみに連続投与することによって、慢性中
毒症状を呈して致死させる全く新しい殺鼠作用をもつも
のである。
Therefore, a wide variety of rodenticides have been developed to prevent the above-mentioned rodent damage, and these rodenticides are mainly mixed with the food that rodents prefer, creating so-called poisonous bait and placing it in passageways and holes. It poisons people to death by feeding them. Compounds conventionally used as such rodenticides include inorganic salts such as yellow phosphorus, nitrous acid, thallium, and barium, as well as organic compounds such as strychnine, and plant-based compounds such as Red Skill, which are used to control field mice. The field mouse typhoid bacillus has been used since the end of the Meiji era, but its use was banned in 1948 due to hygiene reasons. After World War II, synthetic organic rodenticides such as Antu, sodium monofluoroacetate, Warharin, Kastrix, and Muritan were put into practical use one after another, resulting in many developments in the scientific control of rats. Among them,
Marine compounds such as Warharin have a completely new rodenticidal effect, making use of their anticoagulant properties and causing chronic poisoning symptoms and lethality when administered continuously to rats.

(ハ) 発明が解決しようとする問題点ところが、これ
らの殺鼠剤は、ねずみに猛毒であるだけでなく、人畜に
対する毒性もまた強大であることより、その取扱いには
慎重な注意が必要であり、家庭で気軽に使用できるもの
ではなかった。
(c) Problems to be solved by the invention However, these rodenticides are not only highly toxic to rats, but also highly toxic to humans and livestock, so careful attention is required when handling them. It was not something that could be easily used at home.

というのも、薬剤のほとんどがねずみの好む種子や澱粉
質の粉等によって加工され、毒物、及び劇物取締り法に
よる医薬円外毒物に指定され、モノフルオロ酢酸ナトリ
ウムやカストリックス、ムリタンは特定毒物として、そ
の取扱い基準金が定められ、使用制限措置が講じられて
いるからである。
This is because most of the drugs are processed from seeds and starchy powders that mice like, and are designated as non-medicinal poisons under the Poisonous and Deleterious Substances Control Law, and sodium monofluoroacetate, Kastrix, and Muritan are classified as specified poisons. This is because the handling standard has been established and measures have been taken to restrict its use.

従って、殺鼠剤としては、ねずみに忌避されることがな
く、耐薬性を起こさず、致死状態が平静で警戒心を起こ
させず、人畜に対する毒性の低いものが望まれるわけで
あるが、現在の製剤には各々一長一短があり、まだ、満
足すべき段階のものが存在しない。
Therefore, it is desirable for rodenticides to be ones that are not repelled by rats, do not cause drug resistance, have a calm lethal state and do not cause alarm, and have low toxicity to humans and livestock. Each has its advantages and disadvantages, and none of them are at a satisfactory stage yet.

(ニ) 問題点を解決するための手段 そこで、本発明では、主成分たるシキミ酸、トキシン、
アミノ酸、及び、苦参アルカロイドと、副成分たる水、
エタノール、酢酸、及び、酢酸エチルと、触媒として作
用するカラシ配糖体とを混合熟成した後、遠心分離機等
により固液分離すると共に、液状分だけ抽出し、同抽出
液に播生液、シキミ液、菊液、生ヒトデ液、ホルマリン
、ピリジン、及び、エタノールを混入してなるねずみ嫌
畏剤を提供せんとするものである。
(d) Means for solving the problem Therefore, in the present invention, the main components of shikimic acid, toxin,
Amino acids, bitter ginseng alkaloids, and water as a subcomponent,
After mixing and aging ethanol, acetic acid, and ethyl acetate with mustard glycosides that act as a catalyst, solid-liquid separation is performed using a centrifuge, etc., and only the liquid portion is extracted. It is an object of the present invention to provide a mouse repellent which is made by mixing Shikimi liquid, chrysanthemum liquid, raw starfish liquid, formalin, pyridine, and ethanol.

(ホ) 作 用 ねずみ嫌畏剤を使用する際には、ねずみのいそうな場所
に同嫌畏剤を所定の容器に入れて設置しておけば、同嫌
畏剤中に含有された主成分たるシキミ酸、トキシン、ア
ミノ酸、及び、苦参アルカロイドが、副成分たる水、エ
タノール、酢酸、及び、酢酸エチル、並びに、カラシ配
糖体を媒介として化学結合して、小動物、特にねずみの
体内のアミノ酸代謝を抑制する作用成分を形成し、しか
も、同作用成分がホルマリン、ピリジン、及び、エタノ
ールにより揮発されると共に、酢酸エチルの匂いにより
、ねずみが誘導され、この揮発した作用成分を呼吸器系
より吸収すると、神経のバランスが一時的にとれなくな
るものであり、ねずみは、一旦アンバランスな神経のま
ま逃避するが、この動作を繰返すうちにこの匂いが神経
のバランスをくずすことを記憶し、この匂いを忌避する
ようになり、最終的にいなくなるというものである。
(E) Action When using a rodent repellent, place the rodent repellent in a designated container in a place where rodents are likely to be present. The components shikimic acid, toxins, amino acids, and bitter ginseng alkaloids chemically bond through the subcomponents water, ethanol, acetic acid, ethyl acetate, and mustard glycosides, and are absorbed into the bodies of small animals, especially mice. Furthermore, this active ingredient is volatilized by formalin, pyridine, and ethanol, and the odor of ethyl acetate induces mice to absorb this volatilized active ingredient in their respiratory tract. When absorbed from the system, the nervous system becomes temporarily unbalanced, and the mouse runs away with its unbalanced nerves, but as it repeats this action, it remembers that this odor upsets the nervous balance. , they begin to avoid this odor and eventually disappear.

(へ) 効 果 本発明によれば、従来のねずみを殺すという考え方から
、ねずみにFR畏感を与えるという考え方の発想転換を
図り、しかも、同目的を達成することのできるねずみv
&畏剤を製造することができるために、従来、殺鼠剤の
短所、問題点とされていた人畜に対する影響、取扱いの
不便さ、ねずみの死体の腐敗処理困難性、及び、この腐
敗死体による菌の繁殖等を完全に回避、解決することが
でき、しかも、ねずみを匂いで誘導しながら最終的に娘
畏感を与えるために、繁殖力の強いねずみといえども残
らずいなくなるという理想的なねずみ駆除効果を奏する
ものである。
(f) Effects According to the present invention, the idea is changed from the conventional idea of killing mice to giving a sense of FR fear to mice, and moreover, it is possible to create a mouse v that can achieve the same purpose.
Because rodenticides can be manufactured, there have been disadvantages and problems with rodenticides, including their effects on humans and livestock, inconvenience in handling, difficulty in decomposing rodent carcasses, and the possibility of bacterial growth caused by rotting carcasses. It is an ideal mouse extermination method that can completely avoid and solve breeding, etc., and will ultimately eliminate all the mice, even those with a strong breeding ability, in order to guide the mice with scent and give them a sense of awe. It is effective.

(ト) 実施例 本発明の実施例を詳説すれば、ねずみ嫌畏剤は、主成分
たるシキミ酸、トキシン、アミノ酸、及び、苦参アルカ
ロイドと、副成分たる水、エタノール、酢酸、及び、酢
酸エチルと、触媒として作用するカラシ配糖体とを混合
熟成した後、遠心分離機等により固液分離すると共に、
液状分だけ抽出し、同抽出液に潘生液、シキミ液、菊液
、生ヒトデ液、ホルマリン、ピリジン、エタノール、及
び、オレンジオイルを混入させてなるものである。
(g) Example To explain in detail the example of the present invention, the rat repellent contains shikimic acid, toxin, amino acid, and bitter ginseng alkaloid as main components, and water, ethanol, acetic acid, and acetic acid as subcomponents. After mixing and aging ethyl and mustard glycosides that act as a catalyst, solid-liquid separation is performed using a centrifuge, etc.
It is made by extracting only the liquid component and mixing the same extract with Pan sapiensis, shikimi juice, chrysanthemum juice, raw starfish liquid, formalin, pyridine, ethanol, and orange oil.

すなわち、シキミ酸は、ねずみ嫌畏剤の有効成分をつく
る基本成分で、薬草として利用される樒より抽出するこ
とを特徴としており、シキミ酸抽出の際には、樒3kg
と30%濃度のエタノール12kaとを、この順序で所
定第1容器内に投入し、30℃〜35℃の適温状態を保
持せしめて一定期間熟成させるものである。
In other words, shikimic acid is the basic ingredient that makes the active ingredient of the rodent repellent, and is characterized by being extracted from Japanese cypress, which is used as a medicinal herb.
and 12 ka of 30% concentration ethanol are put into a predetermined first container in this order, maintained at an appropriate temperature of 30° C. to 35° C., and aged for a certain period of time.

また、トキシン、及び、アミノ酸は、同(f[剤の有効
成分をつくるのに必要な原料成分で、乾燥させたオニヒ
トデより抽出されるものであり、これらを抽出する際に
は、上記のものとは別個に用意した第2容器中に乾燥ヒ
トデ157に!J、水67向、30%濃度のエタノール
358kg、及び、酢酸20kaを、この順序に投入し
、熟成適温30℃〜35℃にて一定期間漬込み、熟成さ
せるものである。
In addition, toxins and amino acids are the raw materials necessary to make the active ingredients of the drug, and are extracted from dried crown-of-thorns starfish. Into a second container prepared separately from the above, put 157 dried starfish, 67 volumes of water, 358 kg of 30% concentration ethanol, and 20 ka of acetic acid in this order, and heat at a suitable ripening temperature of 30°C to 35°C. It is marinated and aged for a certain period of time.

この際、水は、配合した原料から成分を抽出する働きを
し、また、エタノールは、トキシン、アミノ酸を抽出す
る働きをし、また、酢酸は、熟成後シキミ酸、及び、苦
参カル力ロイドと、トキシン、及び、アミノ酸とを混合
させた際に、これらが化合物を形成しやすくする機能を
有するものである。
At this time, water functions to extract components from the blended raw materials, ethanol functions to extract toxins and amino acids, and acetic acid functions to extract shikimic acid and bitter ginseng calcium chloride after ripening. When mixed with toxin, amino acid, and amino acid, these have the function of making it easier to form a compound.

また、触媒作用をするカラシ配糖体は、濡生50kgと
30%濃度のエタノール150k(]とを、この順序で
上記のものとは別の第3容器に投入し、熱熟成適130
℃〜35℃にて一定期間熟成させるものである。
In addition, mustard glycosides that have a catalytic effect were prepared by putting 50 kg of wet water and 150 kg of 30% ethanol (in this order) into a third container different from the one above, and heating it for 130 kg.
It is aged for a certain period of time at a temperature of 35°C to 35°C.

上記の第1、第2、第3容器内の原料は、気候により6
月〜9月の夏場においては1ケ月間、10〜3月の秋・
冬場においては3ケ月間、そして、4月〜5月の春場に
おいては2ケ月間、半発酵の状態まで漬込むものであり
、この際、各容器内を毎日撹拌して、固液分離が起こら
ないようにするものである。
The raw materials in the first, second and third containers above may vary depending on the climate.
One month in the summer (Monday to September), and one month in the autumn (October to March)
It is steeped for three months in the winter and for two months in the spring from April to May, until it is half fermented. At this time, the inside of each container is stirred every day to prevent solid-liquid separation. This is to prevent it from happening.

そして、上記漬込み期間が経過した後は、第1、第2、
第3容器内の原料合計817kgを、一つの撹拌機内に
入れ、さらに、苦参68kgを加えて約10分間撹拌し
、最後に酢酸エチル8k(lを加えて約10分間撹拌す
るものである。
After the above soaking period has passed, the first, second,
A total of 817 kg of raw materials in the third container were placed in one stirrer, 68 kg of bitter ginseng was added and stirred for about 10 minutes, and finally 8 k (l) of ethyl acetate was added and stirred for about 10 minutes.

この際、くららを切り干しすることにより薬草として利
用される苦参からは、苦参アルカロイドが抽出され、同
苦参アルカロイドがトキシン、及び、アミノ酸と共にシ
キミ酸に作用して成分形成するものであり、また、酢酸
エチルは、配合成分を有効に発揮し、小動物を誘導する
働きをするものである。
At this time, bitter ginseng alkaloids are extracted from bitter ginseng, which is used as a medicinal herb by cutting and drying Kurara, and the bitter ginseng alkaloids act on shikimic acid with toxins and amino acids to form components. Furthermore, ethyl acetate effectively exerts the ingredients and acts to induce small animals.

その後、上記混合撹拌原料893 kaを、遠心分離機
等により固液分離すると共に、液状分だけ683k(1
(76,5%)抽出し、同抽出液中の60kgに、濡生
30に9、シキミ液30kc+、菊の葉より抽出したエ
キスである菊液5kg、生ヒトデ液5kg、ホルマシン
5kg、ピリジン0.5kq、95%濃度のエタノール
14kc+を混合し、同混合物を所定容器に充填する際
に、混合物120kg当り5gのオレンジオイルを添加
することにより、ねずみ嫌畏剤が製品化されるものであ
る。
Thereafter, the 893 ka of mixed and stirred raw materials were separated into solid and liquid using a centrifuge, etc., and only the liquid portion was 683 ka (1 ka).
(76.5%) extracted and added to 60 kg of the same extract, 9 to wet 30, 30 kc+ of Shikimi liquid, 5 kg of chrysanthemum liquid which is an extract extracted from chrysanthemum leaves, 5 kg of raw starfish liquid, 5 kg of formacin, 0 pyridine. A rodent repellent is commercialized by mixing 14kc+ of 95% ethanol and adding 5g of orange oil per 120kg of the mixture when filling the mixture into a predetermined container.

この際、濡生からは触媒作用をするカラシ配糖体が、ま
た、シキミ液からシキミ酸が、また、菊液からは作用成
分を強化する菊の有m、Mが、また、生ヒトデからはト
キシン、アミノ酸が抽出されると共に、これらは半発酵
の状態にて混合されるものであり、ホルマシン、ピリジ
ン、及び、エタノールは、全て作用成分をよく発揮させ
る働きをし、また、オレンジオイルの成分であるオレン
ジ精油が作用成分の強化を行うものである。
At this time, mustard glycosides that have a catalytic effect are obtained from wet plants, shikimic acid is obtained from shikimi juice, and chrysanthemum arum and M, which strengthen the active ingredients, are obtained from raw starfish. Toxins and amino acids are extracted, and these are mixed in a semi-fermented state. Formacin, pyridine, and ethanol all work to enhance the active ingredients, and orange oil. Orange essential oil, which is an ingredient, strengthens the active ingredients.

次に、シキミ酸経路を説明する。すなわち、シキミ酸は
、光合成の産物であるトリオースリン酸エステルよりエ
リスロースー4−リン酸とホスホエノールピルビン酸が
得られ、これらの反応により生じるC7の2−ケトアル
ドン酸のリン酸エステルが閉環して生じるものであり、
同シキミ酸よりホスホエノールピルビン酸との反応によ
るコリスミン酸が生じ、同コリスミン酸よりアントラニ
ル酸を経てセリン関与の下、トリプトファンが生合成さ
れる一方、同コリスミン酸からは、さらにプリフェン酸
を経てフェニルアラニンとチロシンとが各々生合成され
るものである。
Next, the shikimate pathway will be explained. In other words, shikimic acid is produced by erythrose-4-phosphate and phosphoenolpyruvate obtained from triose phosphate, which is a product of photosynthesis, and by ring closure of the C7 phosphate ester of 2-ketoaldonic acid produced by these reactions. It is a thing,
Chorismic acid is produced by the reaction with phosphoenolpyruvate from the same shikimic acid, and tryptophan is biosynthesized from the same chorismic acid via anthranilic acid with the involvement of serine. and tyrosine are each biosynthesized.

以上の様に、シキミ酸経路は、シキミ酸からアミノ酸を
形成するが、その反応形態をかりて、ヒトデから発酵に
よりって生ずるトシキンの付いたアミノ酸を、シキミ酸
が組み込み、次に苦参アルカロイドのマトリンを付けた
分子を構成する。その分子にサフロール、シネオール、
及び、オイゲノールを主成分とするシキミ精油が加わり
芳香するものである。
As mentioned above, in the shikimic acid pathway, amino acids are formed from shikimic acid, but using the reaction form, shikimic acid incorporates the amino acid with toshikin produced by fermentation from starfish, and then the bitter starch alkaloid It constitutes a molecule with matrine attached. Its molecules include safrole, cineole,
Additionally, Shikimi essential oil, whose main component is eugenol, is added to give it a fragrance.

従って、薬草を主体として製品化されたねずみ嫌畏剤を
所定個所に設置しておけば、同嫌畏剤を構成する酢酸エ
チル、ホルマリン、ピリジン、及び、エタノールが作用
成分を揮発させ、しかも、酢酸エチルがねずみを同嫌畏
剤接地場所まで誘導するものであり、誘導されたねずみ
は、作用成分たるシキミ酸、トキシン、アミノ酸、及び
、苦参アルカロイドの化合物を呼吸機系より吸収するこ
とにより、体内のアミノ酸代謝が抑制され、もって神経
のバランスがとれない状態となるものである。そのため
、ねずみは一時的に神経のアンバランスを記憶するため
に逃避するが、この動作を繰り返す内に、上記嫌畏剤よ
り発散される匂いを生理的に嫌悪するようになり、この
匂いのする場所には近づかなくなるものである。
Therefore, if a rodent repellent manufactured mainly from medicinal herbs is placed in a designated location, the ethyl acetate, formalin, pyridine, and ethanol that make up the rodent repellent will volatilize the active ingredients. Ethyl acetate guides mice to the ground where the aphobic agent is located, and the induced mice absorb the active ingredients of shikimic acid, toxins, amino acids, and bitter ginseng alkaloid compounds through their respiratory system. , amino acid metabolism in the body is suppressed, resulting in an imbalanced nervous system. Therefore, the mouse temporarily escapes to memorize the neural imbalance, but as it repeats this action, it becomes physiologically averse to the odor emitted by the above-mentioned fear-repelling agent, and It makes you stay away from the place.

しかも、ねずみ嫌畏剤より揮散される成分は、人畜には
全(影響がなく、むしろ芳香、消臭剤としても機能する
ものである。
Furthermore, the components released by the rodent repellent have no effect on humans or animals, and rather function as fragrances and deodorants.

また、ねずみ嫌畏剤は、揮発成分がすべて揮発されると
、固形分のみが残るわけであるが、同固形分中には苦参
アルカロイド、トキシン等が残存していることにより、
同固形物にゴキブリが接触すると、同ゴキブリの神経が
麻痺されて、ゴキブリの殺虫効果をも果すものである。
In addition, when all the volatile components of rat repellent are volatilized, only the solid content remains, but because bitter ginseng alkaloids, toxins, etc. remain in the solid content,
When a cockroach comes into contact with the solid material, the cockroach's nerves are paralyzed, and it also has an insecticidal effect on cockroaches.

なお、本発明に係るねずみ嫌畏剤は、ねずみに限らず、
小動物一般にも適用可能なものであり、特に、問題の多
いねずみ対して効果が絶大なものである。
In addition, the rat repellent according to the present invention is not limited to rats;
It can be applied to small animals in general, and is particularly effective against mice, which are problematic.

【図面の簡単な説明】[Brief explanation of drawings]

図面はシキミ酸経路の説明図。 The figure is an explanatory diagram of the shikimate pathway.

Claims (1)

【特許請求の範囲】[Claims] 1)主成分たるシキミ酸、トキシン、アミノ酸、及び、
苦参アルカロイドと、副成分たる水、エタノール、酢酸
、及び、酢酸エチルと、触媒として作用するカラシ配糖
体とを混合熟成した後、遠心分離機等により固液分離す
ると共に、液状分だけ抽出し、同抽出液に潘生液、シキ
ミ液、菊液、生ヒトデ液、ホルマリン、ピリジン、及び
、エタノールを混入してなるねずみ嫌畏剤。
1) Main ingredients: shikimic acid, toxin, amino acid, and
After mixing and aging bitter ginseng alkaloids, subcomponents of water, ethanol, acetic acid, and ethyl acetate, and mustard glycosides that act as catalysts, solid-liquid separation is performed using a centrifuge, etc., and only the liquid component is extracted. A rodent repellent is prepared by mixing the same extract with Pan sapiensis liquid, Shikimi liquid, chrysanthemum liquid, raw starfish liquid, formalin, pyridine, and ethanol.
JP60135087A 1985-06-19 1985-06-19 Rodent repellent Granted JPS61291507A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60135087A JPS61291507A (en) 1985-06-19 1985-06-19 Rodent repellent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60135087A JPS61291507A (en) 1985-06-19 1985-06-19 Rodent repellent

Publications (2)

Publication Number Publication Date
JPS61291507A true JPS61291507A (en) 1986-12-22
JPS6332327B2 JPS6332327B2 (en) 1988-06-29

Family

ID=15143524

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60135087A Granted JPS61291507A (en) 1985-06-19 1985-06-19 Rodent repellent

Country Status (1)

Country Link
JP (1) JPS61291507A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02164805A (en) * 1988-12-19 1990-06-25 Norihiko Hayama Mole-repelling agent
WO1999048363A1 (en) * 1998-03-24 1999-09-30 Biolink Technologies Ag Utilization of natural and/or synthetic quinic acid and/or precursors thereof as insect repellents
WO2002076217A1 (en) * 2001-03-22 2002-10-03 Naturobiotech Co., Ltd. Plant extracts composition contained pesticidal activities
JP2018100251A (en) * 2016-12-19 2018-06-28 猛 湯澤 Evasion method of bear and evasion agent

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02164805A (en) * 1988-12-19 1990-06-25 Norihiko Hayama Mole-repelling agent
WO1999048363A1 (en) * 1998-03-24 1999-09-30 Biolink Technologies Ag Utilization of natural and/or synthetic quinic acid and/or precursors thereof as insect repellents
KR20010034611A (en) * 1998-03-24 2001-04-25 바이오링크 테크놀로지스 아게 Utilization of Natural and/or Synthetic Quinic Acid and/or Precursors Thereof As Insect Repellents
WO2002076217A1 (en) * 2001-03-22 2002-10-03 Naturobiotech Co., Ltd. Plant extracts composition contained pesticidal activities
JP2018100251A (en) * 2016-12-19 2018-06-28 猛 湯澤 Evasion method of bear and evasion agent

Also Published As

Publication number Publication date
JPS6332327B2 (en) 1988-06-29

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