JPH03181402A - Method and agent for repelling mouse - Google Patents
Method and agent for repelling mouseInfo
- Publication number
- JPH03181402A JPH03181402A JP32015589A JP32015589A JPH03181402A JP H03181402 A JPH03181402 A JP H03181402A JP 32015589 A JP32015589 A JP 32015589A JP 32015589 A JP32015589 A JP 32015589A JP H03181402 A JPH03181402 A JP H03181402A
- Authority
- JP
- Japan
- Prior art keywords
- rats
- monoterbenes
- camphor
- repellent
- oil
- 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
- 238000000034 method Methods 0.000 title claims description 12
- 230000001846 repelling effect Effects 0.000 title claims description 5
- 239000005871 repellent Substances 0.000 claims abstract description 43
- 230000002940 repellent Effects 0.000 claims abstract description 41
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 claims abstract description 16
- XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 claims abstract description 14
- GRWFGVWFFZKLTI-IUCAKERBSA-N 1S,5S-(-)-alpha-Pinene Natural products CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 claims abstract description 14
- 239000004480 active ingredient Substances 0.000 claims abstract description 10
- GRWFGVWFFZKLTI-UHFFFAOYSA-N α-pinene Chemical compound CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 claims abstract description 10
- WEEGYLXZBRQIMU-UHFFFAOYSA-N Eucalyptol Chemical compound C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229940116229 borneol Drugs 0.000 claims abstract description 9
- -1 n-borneol Chemical compound 0.000 claims abstract description 9
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000005770 Eugenol Substances 0.000 claims abstract description 8
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 claims abstract description 8
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229960002217 eugenol Drugs 0.000 claims abstract description 8
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 claims abstract description 6
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 claims abstract description 5
- NFLGAXVYCFJBMK-BDAKNGLRSA-N (-)-menthone Chemical compound CC(C)[C@@H]1CC[C@@H](C)CC1=O NFLGAXVYCFJBMK-BDAKNGLRSA-N 0.000 claims abstract 6
- NOOLISFMXDJSKH-KXUCPTDWSA-N (-)-Menthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O NOOLISFMXDJSKH-KXUCPTDWSA-N 0.000 claims abstract 4
- 241000700159 Rattus Species 0.000 claims description 70
- NEHNMFOYXAPHSD-UHFFFAOYSA-N citronellal Chemical compound O=CCC(C)CCC=C(C)C NEHNMFOYXAPHSD-UHFFFAOYSA-N 0.000 claims description 12
- 229930003633 citronellal Natural products 0.000 claims description 6
- 235000000983 citronellal Nutrition 0.000 claims description 6
- 239000003094 microcapsule Substances 0.000 abstract description 7
- 239000011248 coating agent Substances 0.000 abstract description 5
- 239000001525 mentha piperita l. herb oil Substances 0.000 abstract description 3
- 235000019477 peppermint oil Nutrition 0.000 abstract description 3
- 239000003795 chemical substances by application Substances 0.000 abstract description 2
- 238000013268 sustained release Methods 0.000 abstract description 2
- 239000012730 sustained-release form Substances 0.000 abstract description 2
- 239000000341 volatile oil Substances 0.000 abstract description 2
- 229930003658 monoterpene Natural products 0.000 abstract 4
- 150000002773 monoterpene derivatives Chemical class 0.000 abstract 4
- 235000002577 monoterpenes Nutrition 0.000 abstract 4
- 244000166675 Cymbopogon nardus Species 0.000 abstract 1
- 235000018791 Cymbopogon nardus Nutrition 0.000 abstract 1
- 239000010624 camphor oil Substances 0.000 abstract 1
- 229960000411 camphor oil Drugs 0.000 abstract 1
- 239000000457 mentha pulegium l. herb oil Substances 0.000 abstract 1
- 230000000694 effects Effects 0.000 description 28
- 238000012360 testing method Methods 0.000 description 21
- 239000003814 drug Substances 0.000 description 13
- 229940079593 drug Drugs 0.000 description 13
- 241000699670 Mus sp. Species 0.000 description 8
- 239000003921 oil Substances 0.000 description 8
- 235000019198 oils Nutrition 0.000 description 8
- 229920000858 Cyclodextrin Polymers 0.000 description 7
- 241001465754 Metazoa Species 0.000 description 7
- 229940041616 menthol Drugs 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 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 7
- 235000013305 food Nutrition 0.000 description 6
- YPHMISFOHDHNIV-FSZOTQKASA-N cycloheximide Chemical compound C1[C@@H](C)C[C@H](C)C(=O)[C@@H]1[C@H](O)CC1CC(=O)NC(=O)C1 YPHMISFOHDHNIV-FSZOTQKASA-N 0.000 description 5
- 230000013872 defecation Effects 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 235000019640 taste Nutrition 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 229960000846 camphor Drugs 0.000 description 4
- 231100000614 poison Toxicity 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 229920001353 Dextrin Polymers 0.000 description 3
- 239000004375 Dextrin Substances 0.000 description 3
- 235000019425 dextrin Nutrition 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000007096 poisonous effect Effects 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000011342 resin composition Substances 0.000 description 3
- 239000003128 rodenticide Substances 0.000 description 3
- NFLGAXVYCFJBMK-RKDXNWHRSA-N (+)-isomenthone Natural products CC(C)[C@H]1CC[C@@H](C)CC1=O NFLGAXVYCFJBMK-RKDXNWHRSA-N 0.000 description 2
- NFLGAXVYCFJBMK-UHFFFAOYSA-N Menthone Chemical compound CC(C)C1CCC(C)CC1=O NFLGAXVYCFJBMK-UHFFFAOYSA-N 0.000 description 2
- 229960005233 cineole Drugs 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 239000003405 delayed action preparation Substances 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 229930007503 menthone Natural products 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 244000052769 pathogen Species 0.000 description 2
- RUMOYJJNUMEFDD-UHFFFAOYSA-N perillyl aldehyde Chemical compound CC(=C)C1CCC(C=O)=CC1 RUMOYJJNUMEFDD-UHFFFAOYSA-N 0.000 description 2
- 239000003380 propellant Substances 0.000 description 2
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 1
- 241000186361 Actinobacteria <class> Species 0.000 description 1
- 206010063659 Aversion Diseases 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 241000723346 Cinnamomum camphora Species 0.000 description 1
- 235000014435 Mentha Nutrition 0.000 description 1
- 241001072983 Mentha Species 0.000 description 1
- 206010035148 Plague Diseases 0.000 description 1
- 241000204357 Porites Species 0.000 description 1
- 206010040880 Skin irritation Diseases 0.000 description 1
- 206010059516 Skin toxicity Diseases 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 238000003975 animal breeding Methods 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 235000019658 bitter taste Nutrition 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- 201000006824 bubonic plague Diseases 0.000 description 1
- 229930008380 camphor Natural products 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- RFFOTVCVTJUTAD-UHFFFAOYSA-N cineole Natural products C1CC2(C)CCC1(C(C)C)O2 RFFOTVCVTJUTAD-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
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- 238000010586 diagram Methods 0.000 description 1
- UMNKXPULIDJLSU-UHFFFAOYSA-N dichlorofluoromethane Chemical compound FC(Cl)Cl UMNKXPULIDJLSU-UHFFFAOYSA-N 0.000 description 1
- 229940099364 dichlorofluoromethane Drugs 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000003255 drug test Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 210000001145 finger joint Anatomy 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
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- 238000010438 heat treatment Methods 0.000 description 1
- 235000003642 hunger Nutrition 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229940040145 liniment Drugs 0.000 description 1
- 239000000865 liniment Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 230000008786 sensory perception of smell Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
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Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
(イ)産業上の利用分野
この発明はモノテルベン類を有効成分とし、安全性及び
作業性の改良されたネズミの忌避方法及びネズミ忌避剤
に関する。
(ロ)従来の技術及び課題
ネズミは分類学上ホ乳綱、ゲッシ目、ねずみ科に属し、
国内では20m1l知られている。このうち住環境で被
害を皮ぼすネズミは、家ネズミと称され、具体的にはド
ブネズミ、ハツカネズミ及びクマネズミの3種である。
これらの家ネズミによる被害は、経済上のものと衛生上
のものとに大別される。
まず経済上の被害としては、従来は農作物や食糧の被害
が注目されたが、国内では食余りの時代であり、あまり
関心が払われなくなってきた。しかし海外からの穀物輸
入の際の船中におけるネズミの被害、又は発展途上国に
おける倉庫での穀物保存中の被害は、今なお大きな問題
となっている。
また、近ごろクローズアップされている被害としては電
気関係設備の被害がある。今日におけろiiE気の高度
利用及びその構造の曳雉化、又コンビ。
−夕による集中制御、管理システムの普及は目覚ましく
、これらにおけるネズミの喫食による被害は甚大t;も
のである。
一方衛生面からみれば、家ネズミは不潔な場所に横機し
ているため、その体外には各種の有害菌例えば腺ペスト
、発疹チフス、鼠咬症等人間に移る多くの病原菌等を有
している場合が多い。従って家ネズミが喫食しなくても
走り珊るだけでこれらの有害な病原菌等を周囲に振り撒
き、それらが原因で衛生上重大な被害をもたらす可能性
かある。
上記ネズミによる被害に対して、殺鼠剤又は防鼠剤(忌
避剤)等の薬剤が用いられたり、捕鼠器が用いられてい
る。このうち殺鼠剤による方法では、殺鼠剤が、昆入さ
れた毒餌の多くは忌避性がありこの毒餌の喫食率は低く
、ネズミにいかに食べさせるかの問題がある。またこの
毒餌を喫食したネズミの症状が激しいとネズミ集団にス
トレスを引き起こし、以後その毒餌に寄り付かなくなる
傾向がある。しかし上記毒餌による忌避効果は、定の空
間からネズミを排除する程に至らない。また、毒餌によ
ってネズミが死んだ場合、その死骸が腐敗し、ハエ等の
発生場所になってさらなる衛生上の問題が生ずることと
なる。
一方忌避剤としては、数種の放線菌が生産する抗生物質
の一種であるシクロヘキシミド(ナラマイシン)が知ら
れている。このナラマイシンは、マイクロカプセル化さ
れ、軟質ポリ塩化ビニル(pvc)等に混練されるなど
して用いられている。
これはネズミにとって嫌な味(収斂性苦味)を示し、ネ
ズミが喫食すると瞬間的にこの嫌な味を知覚し、忌避反
応を示すことを利用している。しかしこの忌避剤は一度
は喫食しないと効果を発揮できないという欠点を有して
いる。またこのナラマイシンの場合、電気設備等の被害
に対しては練り込み等の方法には対処可能であるが、農
産物や食糧の被害等には十分に対応できるものではない
。
この発明はかかる状況に鑑み為されたものであり、安全
かつ効果的に一定の空間からネズミを排除しうろネズミ
忌避方法及びその忌避剤を提供しようとするものである
。
(ハ)amを解決するための手段
かくしてこの発明によれば、ドブネズミ、ハツカネズミ
、クマネズミから選択されたネズミをモノテルベン類で
忌避することを特徴とするネズミの忌避方法、及び、モ
ノテルベン類を有効成分とするネズミ忌避剤か提供され
る。
この発明において、忌避の対象となるドブネズミ、ハツ
カネズミ、クマネズミは、いわゆる家ネズミと称される
ネズミであり、モノテルベン類が単品で上記家ネズミに
対して顕著な忌避作用を有することは、この発明者らに
よって初めて見いだされた知見である。
モノテルベン類は一般的に、化粧品、フレーバー等に使
用されているもので、皮膚刺激、毒性等については安全
性が確認されており、従って人畜に対して非常に安全性
の高い忌避方法及び忌避剤が提供できることとなる。
この発明に用いられる上記モノテルベン類としては、Q
−メントール、Q−メントン、dl−カンフル、n−ボ
ルネオール、1.8−シネオール、オイゲノール、l−
ペリラアルデヒド、d−リモネン、α−ピネン、シトロ
ネラール等が好適なものとして挙げられろ。
上記モノテルベン類は、これらのモノテルベンを実質的
に含有する精油として用いられても良い。
ここで実質的に含有するとは、目的とするモノテルベン
類が、少なくとも約10重量%以上、好ましくは約50
重量%以上を含有することをいう。この例としては例え
ば、e−メントンやa−メントールを実質的に含有して
いるものとして、ハツカ油(ハツカ(Menthaar
vensis L、var、Piperascens
Holmes)及びセイヨウハッカ(lAentha
Piperita L、)から得られるものを含む)、
ベニローヤル油、ハツカ油を脱メントール処理した脱脳
油[別名メントン油(l−メントン含有約70%)又は
ハツカ白油(12−メントン含有約30%)]などを挙
げることができる。
上記モノテルベン類は、ネズミの忌避効果やこのモノテ
ルベンがd用される環境に接触する人間の匂いに対する
嗜好性の点から、1種又は2種以上のブレンドで用いら
れる。
この発明において、上記モノテルベン類を用いてネズミ
を忌避するとは、モノテルベン類がネズミの嗅覚、味覚
等の五感を刺激しうるよう用いられろことをいう。従っ
て、忌避対象空間にモノテルベン類の蒸気が存在しうる
よう用いられる、モノテルベン類を含有した材料を静置
する、ネズミの喫食対象物にモノテルベン類を塗布する
、喫食対象物の成形の際にモノテルベン類を練り込む、
等が挙げられる。
上記モノテルベン類の蒸気を利用する方法は、その蒸気
が存在しうる一定の空間にネズミを寄せ付けないだけで
なく、この空間からネズミを追い出す効果も有し、一定
空間からネズミを有効に排除することができるという利
点を有する。上記モノテルベン類には、それ自身揮発性
のものが多いが、揮発性に乏しい液状や昇華性の無い固
体であっても、モノテルベン類が揮散し得るように用い
られ杷ばよい。この例としては、適当な熱処理をして蒸
気を発生しろろよう用いればよい。
上記のごとくモノテルベン類の蒸気を利用する場合、忌
避対象の所定の空間に有効にモノテルベン類の蒸気が供
給されるように用いられる。例えt。
ば、モノテルベン類を直接又は後述するごとくモノテル
ベン類を含有する徐放性製剤等に製剤化し、これらを忌
避対象の空間に直接静置する、又はシート材、壁材等の
内装用材に含浸・含有して用いる等が挙げられる。また
、直接モノテルベン類の揮散する蒸気を利用する場合、
忌避対象空間にこの蒸気が流れ込むように気体の流れを
構成することが好ましい。
この発明において、用いられる上記モノテルベン類の有
効量は限定できないが、概ね次のような量が目安とされ
る。例えば忌避対象空間にモノテルベン類の蒸気を直接
利用する場合、対象系の温度等により若干異なるが、0
.03g/+2が挙げられる。また忌避対象物に塗布す
る塗布剤に含有してモノテルベン類が用いられる場合は
、塗布面積当りに対して、log/m’の割合が、また
さらに成形物に混練されて用い与れる場合は、成形駒の
重量当り、0.03g/gの割合で用いられる等が挙げ
られる。
この発明において、上記モノテルベン類を実際に施用す
る場合は、他の成分を加えずそのまま単独の形でも使用
できるが、下記するごとく適当な担体等を配合して、モ
ノテルベン類を有効成分として含有する製剤として用い
ることらできる。
上記製剤例として1よ、例えば噴霧剤、油剤、加熱薫蒸
剤、シート、粉剤、粒剤、微粒剤、マイクロカプセル剤
、水和剤等の任意の網形が挙げられる。その調製法は、
有効成分であるモノテルベン類の性質を考慮して、当該
分野で公知の技術を利用すればよい。その−例として、
噴霧剤とするには、上記モノテルベン類を必要に応じ少
量の有機溶媒で希釈し、これにジクロロフルオロメタン
のような酸化ガス噴射剤を用いて作ることができる。
また、マイクロカプセル剤とするには、シクロデキスト
リンその池の包接化合物形成剤の溶液に、有効成分の上
記モノテルベン類を添加し、溶媒除去すればよい。こと
にマイクロカプセル剤とすることは、前記内装用材やネ
ズミの喫食対象物に塗布する塗布剤の調製や喫食対象物
の成形の際に混練する場合の好適な徐放性製剤として提
供でき、忌避効果を持続させる点から好ましい製剤であ
る。
上記マイクロカプセル剤への製剤例としては、シクロデ
キストリンを用いた方法が挙げられる。
この場合、シクロデキストリンにはα−1β−9γ−の
異性体や変性デキストリンとしてメチル基、エチル基の
側鎖をつけた分岐デキストリンがあるが、これらのいず
れを用いてもまたこれらの、見合物でも行うことができ
、目的に応じて適宜選択される。
具体的には水とシクロデキストリンとの99・L〜70
: 30 (重量比)混合物中に、上記有効成分のモ
ノテルベン類又は実質的に該モノテルベン類を含有する
物質を、見合してスラリー液を調製し、これを例えばス
プレードライしてパウダ状の乾燥物とすることにより得
られる。上記シクロデキストリンとしては通常は澱粉の
分解から得られる屋合物をそのまま用いてもよく、この
分解物を精製して所定のシクロデキストリンを単離して
用いてもよい。また上記シクロデキストリンには包接の
対象物質に応じて、デキストリンを、見合して用いろこ
とらできる。上記製剤において、包接対象物質である有
効成分のモノテルベン類は、得られろ乾燥パウダ中に通
常3〜30重量%程度含有されろことが好ましい。
上記のごとく得られるモノテルベン類を含有して徐放性
製剤化されたマイクロカプセル剤は、例えば塗布剤の場
合は、母体の樹脂組成物に対して、該+#i指組戊物の
塗膜性能を阻害せず、かつ有効量の忌避成分を放出しう
るに足る量で用いられる。
具体的には樹脂組成物固形分に対して、約l〜401i
!%の広い範囲で用いることができる。そして上記モノ
テルベン類含有マイクロカプセル剤を上記割合で含有す
る塗布用樹脂組成物は、例えば塗布面積に対してO,Q
l〜O,1g/am″となる量で用いることができる。
(ニ)作用
この発明によれば、モノテルベン類が、ドブネズミ、ハ
ッカネズミ、クマネズミから選択されfこネズミの嗅覚
、味覚等を刺激することにより、ネズミは忌避されるこ
ととはる。
以下実施列によりこの発明の詳細な説明するが、これに
よりこの発明は限定されるものではない。
(以下余白)
(ホ)実施列
忌避試験l
動物飼育用固形飼料に下記薬剤を混練し、24時間後の
飼料喫食量を測定し、忌避性を観察した。
ネズミ4匹(No、1〜4)を1匹ずつ別々に箱に入れ
、このうち2匹(No1.2)に無処理飼料を、池の2
匹(No3.4)に薬剤処理飼料を与えた。結果を下記
〔表1〕に示す。
供試薬剤 局方ハツカ油
忌避対象動物 ラブド ウィスタ系 16週齢薬剤、
昆練割合 9.2%
上記結果から、ハツカ油が混練された飼料を、ラットは
殆ど喫食しないことがわかる。
忌避試験2
上記と同様にして薬剤処理飼料と無処理飼料とを用意し
、ネズミ(上記試験lと同種のもの)3匹(No、 1
〜3)を1匹ずつ箱に入れ、各々に処理飼料と無処理飼
料を与えた。結果を〔表2〕に示す。
注) 上記結果において、No、2のラットが無処理飼
料をlOO%喫食していないのは、このときのラットの
空腹度によるものとおもわれる。
忌避試験3
第1図に示す装置にて、
種々の薬剤蒸気中で飼
料を喫食するかどうかを試験した。
試験装置:合成(12mm厚)を用いて直方体の箱(内
側寸法:縦240mmX +Ii240mmX高さ26
0mm)を作製した。この箱を直y11に3個並べて、
塩化ビニルパイプ(内径
62mm、長さ500mm) (イ)(a)で互いを連
結し、これらが1組で1つの薬剤に対
する試験装置とした。
試験方法、各薬剤試験に対して上記試験装置を2組ずつ
使用し、それぞれを「A」
rBJとして区別した。
・1つの試験装置における3つの箱の
うち、両端の箱には「■」、「■」と
番号付し、給餌器と水を設置した。ま
た中央の箱には水だけ設置した。
・事前に、試験薬剤を設置しない場合
の喫食量を調べた。そして試験装置自
体に対する供試動物の選択性を確認し
た後、喫食が多かった側の箱に試験薬
剤を設置した。
・供試動物はラットを2個体使用し、
常に中央の箱の密閉可能な没入口(ハ)より投入した。
・試験薬剤は、固形のものはIg、液
体のものはlスQ供試した。
・供試動物投入後24時間経過後、「■」。
「■」の箱より給餌器を取り出し、餌
の減少量から喫食率を求め評価を行っ
た。
・供試動物の行動を考察するうえでの
参考として、箱の底部に溜まった糞を
数えて、脱糞敗として記録した。
試験薬剤:12−メントール、Q−メントン、ti、(
1−カンフル、n−ボルネオール、1.8−シネオール
、オイゲノール、l−ペリラアルデヒド、d−リモネン
、α−ピネン、シトロネラール
(以下余白)(a) Industrial Application Field The present invention relates to a rat repellent method and a rat repellent which contain monoterbenes as an active ingredient and have improved safety and workability. (b) Conventional techniques and issues Mice taxonomically belong to the class Holactidae, the order Porites, and the family Rodentidae.
20ml/liter is known in Japan. Among these, the rats that cause damage in the living environment are called house rats, and specifically there are three types: brown rats, house rats, and black rats. The damage caused by these house mice can be broadly classified into economic and sanitary damages. First, in terms of economic damage, damage to crops and food has traditionally been the focus of attention, but now that Japan is living in a time when there is a surplus of food, less attention has been paid to it. However, damage caused by rats on ships when importing grain from overseas, or damage caused while grain is stored in warehouses in developing countries, is still a major problem. In addition, damage to electrical equipment has been attracting attention recently. Today, the advanced use of iiE energy and the transformation of its structure, as well as combinations. - The spread of centralized control and management systems is remarkable, and the damage caused by rats eating them is enormous. On the other hand, from a hygiene perspective, because house mice lie in filthy areas, they carry a variety of harmful bacteria such as bubonic plague, typhus fever, rat bite, and many other pathogens that can be transferred to humans outside their bodies. There are many cases. Therefore, even if house mice do not eat, they can spread these harmful pathogens to the surrounding area just by running around, which can cause serious sanitary damage. To deal with the damage caused by rats, drugs such as rat poison or rat repellent (repellent) are used, and rat traps are used. Among these methods, in the method using rodenticides, many of the poisonous baits in which the rodenticides are introduced are repellent, and the eating rate of these poisonous baits is low, so there is a problem of how to feed the rats. In addition, if rats that eat this poisonous bait develop severe symptoms, it causes stress in the rat population, and they tend not to approach the poisoned bait in the future. However, the repellent effect of the poisoned bait is not sufficient to eliminate rats from a given space. Additionally, if a rat dies from poison bait, its carcass decomposes and becomes a breeding ground for flies, causing further sanitary problems. On the other hand, as a repellent, cycloheximide (naramycin), which is a type of antibiotic produced by several types of actinomycetes, is known. This naramycin is microencapsulated and kneaded into soft polyvinyl chloride (PVC) and the like. This taste is unpleasant to rats (astringent bitterness), and when rats eat it, they instantly perceive this unpleasant taste and take advantage of the fact that they exhibit an aversion reaction. However, this repellent has the disadvantage that it cannot be effective unless it is consumed once. In the case of this naramycin, methods such as kneading can be used to deal with damage to electrical equipment, etc., but cannot sufficiently deal with damage to agricultural products and food. The present invention has been made in view of the above situation, and it is an object of the present invention to provide a method for repelling prowling rats and a repellent thereof, which safely and effectively exclude rats from a certain space. (c) Means for solving am Thus, according to the present invention, there is provided a method for repelling rats, characterized in that rats selected from brown rats, mice, and black rats are repelled with monoterbenes, and monoterbenes are used as an active ingredient. A rat repellent will be provided. In this invention, brown rats, mice, and black rats that are to be repelled are rats called so-called house rats, and the inventors have discovered that monoterbenes alone have a remarkable repellent effect on the above-mentioned house rats. This finding was first discovered by et al. Monoterbenes are generally used in cosmetics, flavors, etc., and their safety in terms of skin irritation and toxicity has been confirmed, making them extremely safe repellent methods and repellents for humans and animals. can be provided. The monoterbenes used in this invention include Q
-Menthol, Q-menthone, dl-camphor, n-borneol, 1.8-cineole, eugenol, l-
Suitable examples include perillaldehyde, d-limonene, α-pinene, citronellal, and the like. The monoterbenes mentioned above may be used as essential oils substantially containing these monoterbenes. Here, "substantially containing" means that the target monoterbenes are at least about 10% by weight or more, preferably about 50% by weight.
% by weight or more. Examples of this include, for example, peppermint oil (Menthaar oil), which substantially contains e-menthone and a-menthol.
vensis L, var, Piperascens
Holmes) and Mentha (lAentha)
Piperita L.),
Examples include beniroyal oil and dementholized oil obtained by removing menthol from heart oil (also known as menthone oil (contains about 70% l-menthon) or heart white oil (contains about 30% 12-menthon)). The above-mentioned monoterbenes are used singly or in a blend of two or more, from the viewpoint of the rat repellent effect and the taste preference of humans who come into contact with the environment in which the monoterbenes are used. In this invention, using the monoterbenes to repel rats means that the monoterbenes are used so as to stimulate the five senses of rats, such as smell and taste. Therefore, monoterbenes are used so that the vapor of monoterbenes can exist in the space to be repelled, materials containing monoterbenes are left standing, monoterbenes are applied to objects to be eaten by rats, and monoterbenes are used when molding objects to be eaten. knead the kind,
etc. The method of using the vapor of the monoterbenes mentioned above not only keeps rats away from a certain space where the vapor may exist, but also has the effect of expelling rats from this space, making it possible to effectively eliminate rats from a certain space. It has the advantage of being able to Many of the monoterbenes themselves are volatile, but even liquids with poor volatility or solids with no sublimation properties may be used in a manner that allows the monoterbenes to be volatilized. In this case, a suitable heat treatment may be used to generate steam. When using the vapor of monoterbenes as described above, the vapor of monoterbenes is used so as to be effectively supplied to a predetermined space to be avoided. Example t. For example, using monoterbenes directly or formulating them into sustained-release preparations containing monoterbenes as described below and leaving them directly in the space to be avoided, or impregnating and containing them in interior materials such as sheet materials and wall materials. For example, it can be used as In addition, when directly using the volatilized vapor of monoterbenes,
It is preferable to configure the gas flow so that this vapor flows into the space to be avoided. In this invention, the effective amount of the monoterbenes used cannot be limited, but the following amounts are generally used as a guide. For example, when using monoterbenes vapor directly in a space to be avoided, it may vary slightly depending on the temperature of the target system, but 0.
.. 03g/+2 is mentioned. In addition, when monoterbenes are used in a coating agent to be applied to objects to be avoided, the ratio of log/m' to the applied area is determined, and when the monoterbenes are used after being kneaded into a molded article, For example, it may be used at a rate of 0.03 g/g based on the weight of the molded piece. In this invention, when the above monoterbenes are actually applied, they can be used alone as they are without adding other ingredients, but they can be mixed with a suitable carrier as described below to contain the monoterbenes as an active ingredient. It can be used as a preparation. Examples of the above-mentioned formulations include arbitrary net forms such as sprays, oils, heated fumigants, sheets, powders, granules, fine granules, microcapsules, and wettable powders. Its preparation method is
Techniques known in the art may be used in consideration of the properties of monoterbenes as active ingredients. As an example,
A propellant can be prepared by diluting the above monoterbenes with a small amount of an organic solvent, if necessary, and using an oxidizing gas propellant such as dichlorofluoromethane. Further, in order to form microcapsules, the above-mentioned monoterbenes as active ingredients may be added to a solution of the cyclodextrin clathrate compound forming agent, and the solvent may be removed. In particular, microcapsules can be provided as a suitable sustained-release preparation for preparation of coating agents applied to the interior materials and objects to be eaten by rats, and when kneaded during the molding of objects to be eaten. This is a preferable formulation from the viewpoint of sustaining the effect. An example of formulation into the above-mentioned microcapsules includes a method using cyclodextrin. In this case, cyclodextrin includes α-1β-9γ-isomers and branched dextrins with methyl and ethyl group side chains as modified dextrins. It can also be done, and is selected as appropriate depending on the purpose. Specifically, water and cyclodextrin from 99.L to 70
: 30 (weight ratio) A slurry liquid is prepared by adding the above-mentioned active ingredient monoterbenes or a substance substantially containing the monoterbenes to the mixture, and then spray-drying this, for example, to obtain a powder-like dry product. It can be obtained by As the above-mentioned cyclodextrin, a compound obtained from the decomposition of starch may be used as it is, or the decomposition product may be purified to isolate a desired cyclodextrin for use. Further, dextrin can be used in accordance with the substance to be included in the above-mentioned cyclodextrin. In the above formulation, it is preferable that the active ingredient monoterbenes, which are clathrate substances, be contained in the resulting dry powder in an amount of usually about 3 to 30% by weight. For example, in the case of a liniment, the microcapsule prepared as a sustained-release formulation containing monoterbenes obtained as described above is applied to the base resin composition to form a coating film of the +#i finger joint. It is used in an amount sufficient to release an effective amount of repellent component without impeding performance. Specifically, about 1 to 401 i based on the solid content of the resin composition.
! It can be used in a wide range of %. The resin composition for coating containing the monoterbenes-containing microcapsules in the proportions described above has, for example,
(d) Effect: According to the present invention, the monoterbenes are selected from brown rats, myna rats, and black rats, and stimulate the sense of smell, taste, etc. of the rats. By doing so, rats are repelled.The present invention will be described in detail with reference to practical rows below, but the present invention is not limited thereby.(The following is a blank space) (e) Practical row repellent test l The following chemicals were mixed into solid feed for animal breeding, and the amount of feed consumed after 24 hours was measured to observe the repellency. 4 mice (No. 1 to 4) were placed individually in a box, Two of them (No. 1.2) were given untreated feed, and two of them in the pond were fed untreated feed.
The animal (No. 3.4) was given drug-treated feed. The results are shown in Table 1 below. Test drug: Pharmacopoeia oil repellent Target animal: Rhabdo Wista 16-week-old drug,
Kneading ratio: 9.2% From the above results, it can be seen that rats hardly eat the feed mixed with peppermint oil. Repellent test 2 Drug-treated feed and untreated feed were prepared in the same manner as above, and 3 rats (same species as in test 1 above) (No. 1,
~3) were placed one by one in a box, and each was given treated feed and untreated feed. The results are shown in [Table 2]. Note) In the above results, the reason why rats No. 2 did not eat 100% of the untreated feed is thought to be due to the hunger level of the rats at this time. Repellency Test 3 Using the apparatus shown in Figure 1, a test was conducted to determine whether feed could be eaten in the presence of various drug vapors. Test equipment: Synthetic (12 mm thick) rectangular parallelepiped box (inside dimensions: length 240 mm x +Ii 240 mm x height 26
0 mm) was produced. Line up 3 of these boxes directly on y11,
Vinyl chloride pipes (inner diameter 62 mm, length 500 mm) (a) were connected to each other with (a), and one set of these was used as a test device for one drug. Test Method: Two sets of the above test apparatus were used for each drug test, and each was distinguished as "A" rBJ. - Among the three boxes in one test device, the boxes at both ends were numbered "■" and "■", and a feeder and water were installed. In addition, only water was placed in the central box.・We investigated in advance the amount of food consumed without the test drug. After confirming the selectivity of the test animals to the test device itself, the test drug was placed in the box on the side that had been eaten the most. -Two rats were used as the test animals, and they were always introduced through the sealable immersion opening (c) in the central box. - The test drugs used were Ig (solid) and IsuQ (liquid). - 24 hours after introducing the test animal, "■". The feeder was taken out from the box labeled "■", and the eating rate was determined from the amount of food lost and evaluated.・As a reference when considering the behavior of the test animals, the feces collected at the bottom of the box were counted and recorded as defecation losses. Test drugs: 12-menthol, Q-menthone, ti, (
1-camphor, n-borneol, 1.8-cineole, eugenol, l-periraldehyde, d-limonene, α-pinene, citronellal (margin below)
が水分を吸収したものと思われる。
ラットでは、e−メントール処理した箱(■)内での喫
食や脱糞がみられず忌避効果が認められた。
[12−メントンの忌避効果]
(以下余白)
が水分を吸収したものと思われろ。
ラットでは、Q−メントン処理した箱(■)内での喫食
や脱糞がみられず忌避効果が認められた。
[d12−カンフルの忌避効果]
が水分を吸収したものと思われる。
ラットでは、dl−カンフル処理した箱(■)内での喫
食や脱糞がみられず忌避効果が認められた。seems to have absorbed water. In rats, no eating or defecating was observed in the e-menthol treated box (■), indicating a repellent effect. [12-Repellent effect of menthone] It is thought that (the following margin) has absorbed moisture. In rats, no eating or defecating was observed in the Q-menthon-treated box (■), indicating a repellent effect. [d12-Camphor repellent effect] It is thought that the d12-camphor repellent effect absorbed moisture. In rats, no eating or defecating was observed in the dl-camphor-treated box (■), indicating a repellent effect.
ラットでは、 n−ボルネオール処理した箱(■) 内での喫食や脱糞かみられず忌避効果が認められた。 In rats, Box treated with n-borneol (■) No eating or defecating was observed inside the cage, indicating a repellent effect.
【1.8−シネオールの忌避効果】 ラットでは、 1.8−シネオール処理した箱(■) 内での喫食や脱糞がみられず忌避効果が認められた。[1.8-Repellent effect of cineole] In rats, 1.8-Cineol treated box (■) No eating or defecating was observed inside the cage, indicating a repellent effect.
ラットでは、
オイゲノール処理した箱(■)に
は忌避効果は認められるが、
少量の喫食や脱糞が
みられた。
ラットでは、
ペリラアルデヒド処理した箱(■
)には忌避効果は認められろが、
少量の喫食や脱
糞がみられた。
ラットでは、d−リモネン処理した箱(■)には忌避効
果は認められるが、少量の喫食や脱糞かみられた。
ラットでは、α−ピネン処理した箱(■)には忌避効果
は認められるか、少量の喫食や脱糞がみられた。In rats, although a repellent effect was observed in the eugenol-treated box (■), a small amount of eating and defecation were observed. In rats, although a repellent effect was observed in the box treated with perilaldehyde (■), a small amount of eating and defecation were observed. In rats, although a repellent effect was observed in the d-limonene-treated box (■), a small amount of eating and defecation were observed. In rats, a repellent effect was observed in the α-pinene-treated box (■), or a small amount of eating and defecation were observed.
*)24時間後の餌重量が増加したのは、装置内の湿度
が高いため餌が水分を吸収したらのと思われる。
ラットでは、シトロネラール処理した箱(■)内での喫
食や脱糞がみられず忌避効果が認められ〔結果〕
以上の結果から、Q−メントール、Q−メントン、dl
−カンフル、n−ボルネオール、1.8−ンネオール、
シトロネラールの6つの薬剤については、これらを設置
した箱での餌の喫食がなく、ラットに対して忌避効果が
認められた。
一方、オイゲノール、1−ペリラアルデヒド、dリモネ
ン、α−ピネンの4つの薬剤についても忌避効果は認め
与れたが、いずれら少量の喫食があった。
(へ)発明の効果
この発明によれば、モノテルベン類により家ネズミを有
効に忌避することかできる。−窓空間から排除すること
ができろ。*) The reason why the weight of the bait increased after 24 hours is probably because the bait absorbed water due to the high humidity inside the device. In rats, no eating or defecating was observed in the citronellal-treated box (■), and a repellent effect was observed. [Results] From the above results, Q-menthol, Q-menthone,
- camphor, n-borneol, 1.8-neol,
Regarding the six citronellal drugs, no rats ingested the food in the boxes in which they were placed, indicating that they had a repellent effect on rats. On the other hand, four drugs, eugenol, 1-periraldehyde, d-limonene, and α-pinene, were also found to have repellent effects, but a small amount of them were consumed. (f) Effects of the Invention According to the present invention, house mice can be effectively repelled using monoterbenes. - Be able to exclude it from the window space.
第1図はモノテルベン類によるネズミの忌避効果を試験
する試験装置の構成説明図である。FIG. 1 is an explanatory diagram of the configuration of a test device for testing the rat repellent effect of monoterbenes.
Claims (1)
れたネズミをモノテルベン類で忌避することを特徴とす
るネズミの忌避方法。 2、モノテルベン順が、l−メントール、l−メントン
、dl−カンフル、n−ボルネオール、1,8−シネオ
ール、オイゲノール、l−ペリラアルデヒド、d−リモ
ネン、α−ピネン、シトロネラールから選択される1種
又は2種以上である請求項1記載の方法。 3、モノテルベン類を有効成分とするネズミ忌避剤。 4、モノテルベン類が、l−メントール、l−メントン
、dl−カンフル、n−ボルネオール、1,8−シネオ
ール、オイゲノール、l−ペリラアルデヒド、d−リモ
ネン、α−ピネン、シトロネラールから選択される1種
又は2種以上である請求項3記載のネズミ忌避剤。[Scope of Claims] 1. A method for repelling rats, which comprises repelling rats selected from brown rats, house rats, and black rats using monoterbenes. 2. One monoterbene selected from l-menthol, l-menthone, dl-camphor, n-borneol, 1,8-cineole, eugenol, l-periraldehyde, d-limonene, α-pinene, and citronellal. or 2 or more types. 3. A rat repellent containing monoterbenes as an active ingredient. 4. One type of monoterbenes selected from l-menthol, l-menthone, dl-camphor, n-borneol, 1,8-cineole, eugenol, l-periraldehyde, d-limonene, α-pinene, and citronellal or 2 or more types of rat repellents according to claim 3.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP32015589A JPH03181402A (en) | 1989-12-08 | 1989-12-08 | Method and agent for repelling mouse |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP32015589A JPH03181402A (en) | 1989-12-08 | 1989-12-08 | Method and agent for repelling mouse |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03181402A true JPH03181402A (en) | 1991-08-07 |
Family
ID=18118322
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP32015589A Pending JPH03181402A (en) | 1989-12-08 | 1989-12-08 | Method and agent for repelling mouse |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03181402A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0648903A (en) * | 1992-07-08 | 1994-02-22 | Azetsukusu:Kk | Synthetic resin composition |
WO2008078594A1 (en) * | 2006-12-27 | 2008-07-03 | Earth Chemical Co., Ltd. | Method for repelling rat or mouse, method for capturing rat or mouse, and repellent for rat or mouse |
JP2008162906A (en) * | 2006-12-27 | 2008-07-17 | Earth Chem Corp Ltd | Rat repellent |
JP2009023921A (en) * | 2007-07-18 | 2009-02-05 | Earth Chem Corp Ltd | Method for capturing rat |
JP2009023939A (en) * | 2007-07-19 | 2009-02-05 | Earth Chem Corp Ltd | Method for repelling rat |
WO2022066785A1 (en) * | 2020-09-23 | 2022-03-31 | Oms Investments, Inc. | Mouse repellents, devices, and methods of using such |
-
1989
- 1989-12-08 JP JP32015589A patent/JPH03181402A/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0648903A (en) * | 1992-07-08 | 1994-02-22 | Azetsukusu:Kk | Synthetic resin composition |
WO2008078594A1 (en) * | 2006-12-27 | 2008-07-03 | Earth Chemical Co., Ltd. | Method for repelling rat or mouse, method for capturing rat or mouse, and repellent for rat or mouse |
JP2008162906A (en) * | 2006-12-27 | 2008-07-17 | Earth Chem Corp Ltd | Rat repellent |
JP2009023921A (en) * | 2007-07-18 | 2009-02-05 | Earth Chem Corp Ltd | Method for capturing rat |
JP2009023939A (en) * | 2007-07-19 | 2009-02-05 | Earth Chem Corp Ltd | Method for repelling rat |
WO2022066785A1 (en) * | 2020-09-23 | 2022-03-31 | Oms Investments, Inc. | Mouse repellents, devices, and methods of using such |
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