JPH03133904A - Insect pest-repellent - Google Patents
Insect pest-repellentInfo
- Publication number
- JPH03133904A JPH03133904A JP27314489A JP27314489A JPH03133904A JP H03133904 A JPH03133904 A JP H03133904A JP 27314489 A JP27314489 A JP 27314489A JP 27314489 A JP27314489 A JP 27314489A JP H03133904 A JPH03133904 A JP H03133904A
- Authority
- JP
- Japan
- Prior art keywords
- repellent
- derivative
- ether
- phenyl ether
- ants
- 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
- 239000005871 repellent Substances 0.000 title claims abstract description 38
- 241000238631 Hexapoda Species 0.000 title abstract description 16
- 230000002940 repellent Effects 0.000 claims abstract description 37
- 241000607479 Yersinia pestis Species 0.000 claims abstract description 22
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims abstract description 22
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical compound C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000000203 mixture Substances 0.000 claims abstract description 12
- 150000003862 amino acid derivatives Chemical class 0.000 claims abstract description 5
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 5
- 229930195729 fatty acid Natural products 0.000 claims abstract description 5
- 239000000194 fatty acid Substances 0.000 claims abstract description 5
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 5
- 239000007787 solid Substances 0.000 claims abstract description 5
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 4
- 239000000057 synthetic resin Substances 0.000 claims abstract description 4
- 239000010408 film Substances 0.000 claims abstract 2
- 239000001993 wax Substances 0.000 claims description 3
- 229920002994 synthetic fiber Polymers 0.000 claims description 2
- 239000012209 synthetic fiber Substances 0.000 claims description 2
- 241001674044 Blattodea Species 0.000 abstract description 10
- 238000004891 communication Methods 0.000 abstract description 8
- 244000144972 livestock Species 0.000 abstract description 6
- 239000000843 powder Substances 0.000 abstract description 4
- 239000000835 fiber Substances 0.000 abstract description 3
- 239000004615 ingredient Substances 0.000 abstract description 3
- HZVFRKSYUGFFEJ-YVECIDJPSA-N (2r,3r,4s,5r)-7-phenylhept-6-ene-1,2,3,4,5,6-hexol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=CC1=CC=CC=C1 HZVFRKSYUGFFEJ-YVECIDJPSA-N 0.000 abstract description 2
- 108010010803 Gelatin Proteins 0.000 abstract description 2
- 239000000499 gel Substances 0.000 abstract description 2
- 239000008273 gelatin Substances 0.000 abstract description 2
- 229920000159 gelatin Polymers 0.000 abstract description 2
- 235000019322 gelatine Nutrition 0.000 abstract description 2
- 235000011852 gelatine desserts Nutrition 0.000 abstract description 2
- 229910052920 inorganic sulfate Inorganic materials 0.000 abstract description 2
- 150000001719 carbohydrate derivatives Chemical class 0.000 abstract 2
- 239000004480 active ingredient Substances 0.000 abstract 1
- 239000002775 capsule Substances 0.000 abstract 1
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- 230000008023 solidification Effects 0.000 abstract 1
- 238000007711 solidification Methods 0.000 abstract 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 abstract 1
- 231100000331 toxic Toxicity 0.000 abstract 1
- 230000002588 toxic effect Effects 0.000 abstract 1
- 241000257303 Hymenoptera Species 0.000 description 19
- 238000012360 testing method Methods 0.000 description 15
- 230000000694 effects Effects 0.000 description 11
- 241000894007 species Species 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 8
- 239000002917 insecticide Substances 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 6
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- 241000722666 Camponotus Species 0.000 description 3
- ZNOLGFHPUIJIMJ-UHFFFAOYSA-N fenitrothion Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C(C)=C1 ZNOLGFHPUIJIMJ-UHFFFAOYSA-N 0.000 description 3
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- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
- 241000238876 Acari Species 0.000 description 2
- 241000238657 Blattella germanica Species 0.000 description 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
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- 239000000853 adhesive Substances 0.000 description 2
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- 125000003118 aryl group Chemical group 0.000 description 2
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- SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
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- 150000001875 compounds Chemical class 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 239000012362 glacial acetic acid Substances 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 230000009931 harmful effect Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000000077 insect repellent Substances 0.000 description 2
- 231100000053 low toxicity Toxicity 0.000 description 2
- 239000008204 material by function Substances 0.000 description 2
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- 239000004745 nonwoven fabric Substances 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 150000003505 terpenes Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 description 1
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 description 1
- DTTDXHDYTWQDCS-UHFFFAOYSA-N 1-phenylcyclohexan-1-ol Chemical compound C=1C=CC=CC=1C1(O)CCCCC1 DTTDXHDYTWQDCS-UHFFFAOYSA-N 0.000 description 1
- ZBVDYZBXFDCDDF-UHFFFAOYSA-N 2,3,6-trimethylbenzamide Chemical compound CC1=CC=C(C)C(C(N)=O)=C1C ZBVDYZBXFDCDDF-UHFFFAOYSA-N 0.000 description 1
- CTOLFOYOXKUZKO-UHFFFAOYSA-N 2,3-dipropylpyridine Chemical compound CCCC1=CC=CN=C1CCC CTOLFOYOXKUZKO-UHFFFAOYSA-N 0.000 description 1
- DSKYSDCYIODJPC-UHFFFAOYSA-N 2-butyl-2-ethylpropane-1,3-diol Chemical compound CCCCC(CC)(CO)CO DSKYSDCYIODJPC-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 241000254032 Acrididae Species 0.000 description 1
- 241000238662 Blatta orientalis Species 0.000 description 1
- 241000238660 Blattidae Species 0.000 description 1
- OKIJSNGRQAOIGZ-UHFFFAOYSA-N Butopyronoxyl Chemical group CCCCOC(=O)C1=CC(=O)CC(C)(C)O1 OKIJSNGRQAOIGZ-UHFFFAOYSA-N 0.000 description 1
- NRHKXIOFEQMAAH-UHFFFAOYSA-N C(C)C1=C(C(=C(C(=O)N)C=C1)Cl)CC Chemical compound C(C)C1=C(C(=C(C(=O)N)C=C1)Cl)CC NRHKXIOFEQMAAH-UHFFFAOYSA-N 0.000 description 1
- 241000426451 Camponotus modoc Species 0.000 description 1
- 241000258920 Chilopoda Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 235000015001 Cucumis melo var inodorus Nutrition 0.000 description 1
- 240000002495 Cucumis melo var. inodorus Species 0.000 description 1
- 241000256057 Culex quinquefasciatus Species 0.000 description 1
- ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 description 1
- XTJFFFGAUHQWII-UHFFFAOYSA-N Dibutyl adipate Chemical compound CCCCOC(=O)CCCCC(=O)OCCCC XTJFFFGAUHQWII-UHFFFAOYSA-N 0.000 description 1
- YUXIBTJKHLUKBD-UHFFFAOYSA-N Dibutyl succinate Chemical compound CCCCOC(=O)CCC(=O)OCCCC YUXIBTJKHLUKBD-UHFFFAOYSA-N 0.000 description 1
- 241000255925 Diptera Species 0.000 description 1
- 241001507629 Formicidae Species 0.000 description 1
- 241001466042 Fulgoromorpha Species 0.000 description 1
- 239000005792 Geraniol Substances 0.000 description 1
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 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 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 241000238814 Orthoptera Species 0.000 description 1
- 208000002193 Pain Diseases 0.000 description 1
- 241000048273 Periplaneta japonica Species 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 description 1
- 241000238711 Pyroglyphidae Species 0.000 description 1
- ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 description 1
- 241000978776 Senegalia senegal Species 0.000 description 1
- 239000000877 Sex Attractant Substances 0.000 description 1
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- VEGOPIRPQIZFRD-UVHWXNHCSA-N [(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl] (e)-3-(4-hydroxyphenyl)prop-2-enoate Chemical compound O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1OC(=O)\C=C\C1=CC=C(O)C=C1 VEGOPIRPQIZFRD-UVHWXNHCSA-N 0.000 description 1
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- 229910052782 aluminium Inorganic materials 0.000 description 1
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- 125000000129 anionic group Chemical group 0.000 description 1
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- WLJVXDMOQOGPHL-UHFFFAOYSA-N benzyl-alpha-carboxylic acid Natural products OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 1
- JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000000073 carbamate insecticide Substances 0.000 description 1
- 230000007910 cell fusion Effects 0.000 description 1
- 230000031902 chemoattractant activity Effects 0.000 description 1
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 1
- 235000000484 citronellol Nutrition 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
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- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
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- 229960001673 diethyltoluamide Drugs 0.000 description 1
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 1
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- 229940046533 house dust mites Drugs 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
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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、ゴキブリ、ハエ、力、イエダニ等17生害虫
、アブラムシ、ウンカ、ダニ、メイ虫等の農林害虫又は
アリ、イガ、ムカデ等の一般害虫の忌避剤に関するもの
で、特にゴキブリ、アリ類に対する忌避剤として有用な
忌避組成物に関する。[Detailed Description of the Invention] [Field of Industrial Application] The present invention is applicable to 17 living pests such as cockroaches, flies, grasshoppers, house dust mites, agricultural and forestry pests such as aphids, plant hoppers, mites, and insects, or ants, burrs, centipedes, etc. The present invention relates to a repellent for general pests, and particularly to a repellent composition useful as a repellent for cockroaches and ants.
害虫の防除剤としては、従来より農林害虫殺虫剤として
多種類のものが用いられている。Many types of pest control agents have been used in the past as agricultural and forestry pest insecticides.
衛生害虫殺虫剤としては、これら農用殺虫剤のうち人畜
に毒性の少ない医薬用殺虫剤として選択され使用が許可
されている。Among these agricultural insecticides, pharmaceutical insecticides that are less toxic to humans and livestock are selected as sanitary pest insecticides, and their use is permitted.
また、チリダニ、アリ、イガ等一般雑害虫に対しては不
快害虫防除剤として、その使用の自主規制が行われてい
る。In addition, voluntary regulations have been put in place for its use as an unpleasant pest control agent against general pests such as dust mites, ants, and burrs.
一方、近来さらに研究が重ねられ従来から粘着剤等物理
的捕捉又これに誘因剤を加えて効果を倍加させたり、昆
虫生育ステージの産卵・羽化及び羽化の一段階の生育生
理を撹乱して防除する生育阻害剤も防除の新規なものと
して重用され始めた。On the other hand, in recent years, further research has been carried out, and conventional techniques include physical trapping such as adhesives, adding attractants to this to double the effect, and disrupting the growth physiology of the insect growth stages of spawning, emergence, and emergence. Growth inhibitors have also begun to be used as new control agents.
また、さらに微生物を利用した生物工学の利用により、
バチ二ルスチニリンゲンス等、菌体に生成する結晶毒素
の殺虫力を利用したBT剤、天敵産卵不妊処理をした昆
虫個体の利用、昆虫のもつフェロモン特に性フェロモン
或いは交信攪拌を利用したフェロモンが殺虫剤捕虫器材
と併用利用したものが環境生態系を壊さず好効果をあら
れしている。Furthermore, through the use of bioengineering using microorganisms,
BT agents that utilize the insecticidal power of crystalline toxins produced in bacterial cells such as B. batinirustinylingens, the use of insect individuals that have been sterilized to spawn by their natural enemies, and pheromones possessed by insects, particularly sex pheromones, or pheromones that utilize communication agitation. When used in combination with insecticides and insect trapping equipment, it has shown good effects without destroying the environmental ecosystem.
また、植物由来のピレトリン、ロチノン、ニコチン等も
使用されている歴史があり、近時遺伝子操作、細胞融合
1組織培養等でジオキサビシクロオクタン(ハエドクソ
ウ)や他の植物由来殺虫剤、抗生物質の利用等、その開
発進歩が目覚ましい。In addition, there is a history of the use of plant-derived pyrethrin, rotinone, nicotine, etc., and in recent years, genetic manipulation, cell fusion, tissue culture, etc. The development progress in terms of usage, etc. is remarkable.
昆虫は自然の摂理によって生育し、人畜に有害な作用を
与える部門、例えば農林作物、人畜の生活環境、工業材
料等の害虫の危害等を示すが、これを防止するためには
、忌避剤が最も合理的な防除法である。Insects grow according to the laws of nature, and pose harmful effects to humans and livestock, such as agricultural and forestry crops, the living environment of humans and livestock, and industrial materials.In order to prevent this, repellents are needed. This is the most rational control method.
従来より農林作物の害虫忌避剤として、ベンズアルデヒ
ド、ベンジルベンゾエート、ブチルエチルプロパンジオ
ール、ブトピロノキシル、ブチルアセトアニリド、ブチ
ルカルピトールアセテート。Benzaldehyde, benzyl benzoate, butylethylpropanediol, butopyronoxyl, butylacetanilide, and butylcarpitol acetate have traditionally been used as pest repellents for agricultural and forestry crops.
ブトキシポリプロピレングリコール、クロルフルアミド
、シトロネロール、クレゾール、ジブチルアジペート、
ジブチルフタレート、ジブチルサクシネート、ジメチル
トルアミド、ジエチルトルアミド、ジメチルフタレート
、ジフェニルアミン。Butoxypolypropylene glycol, chlorfluamide, citronellol, cresol, dibutyl adipate,
Dibutyl phthalate, dibutyl succinate, dimethyltoluamide, diethyltoluamide, dimethyl phthalate, diphenylamine.
エチルヘキサンジオール、ジエチルクロロベンズアミド
、オクタヒドロジベンゾフランカルバルデヒド、ジプロ
ピルピリジン力ルポキシレート、オクタチオエタノール
、β−ナフトール、フェニルシクロヘキサノール、テト
ラヒドロチオフェン。Ethylhexanediol, diethylchlorobenzamide, octahydrodibenzofurancarbaldehyde, dipropylpyridine urupoxylate, octathioethanol, β-naphthol, phenylcyclohexanol, tetrahydrothiophene.
ゲラニオール、テルペノイド等があり、広範囲に利用さ
れている。It contains geraniol, terpenoids, etc., and is widely used.
本発明の対象害虫特にゴキブリはアブラムシとも言われ
、直翅目ゴキブリ亜目に属する昆虫の総称で、その種類
も多く世界に広く分布している。Cockroaches, which are the target pests of the present invention, are also called aphids and are a general term for insects belonging to the order Orthoptera, suborder Cockroaches, and there are many types of them and they are widely distributed throughout the world.
しかし、もともとは、熱帯、亜熱帯に住む昆虫であるが
、交通機関の発達により、日本では約30種(7科18
種)で多くは屋外で生活するが、近時室内暖房設備の完
備、食料の豊富化により分布及び生息密度を広げている
。特にクロゴキブリ、チャバネゴキブリ、ヤマトゴキブ
リ、ワモンゴキブリが主に棲息し、人家内に定住徘徊し
、汚物を好み、病原菌を伝播するため、重要な衛生害虫
と目されている。However, although they originally live in the tropics and subtropics, due to the development of transportation, Japan now has about 30 species (7 families, 18 species).
(species) and most of them live outdoors, but with the recent introduction of indoor heating equipment and an abundance of food, their distribution and population density have expanded. In particular, black cockroaches, German cockroaches, Japanese cockroaches, and American cockroaches mainly inhabit people's homes, and they are considered important sanitary pests because they like filth and spread pathogens.
また、近時オフィスオートメーションの発達により、コ
、ンピニーターを始め種々のOA機器にもそのビル内雰
囲気及び機器内の適温性により、絶好の棲息場所として
多数の個体が見られるようになり、二次的にその機器機
能に妨害を示すようになった。また、ボックス型の食品
・飲料自動販売機もその簡便さの特徴のもと現在多種多
様のものが数多く設置され、この中にもゴキブリが出没
するようになった。これを防除するため、殺虫剤を用い
るときは、密閉機器中への散布施薬法も毒餌や殺虫忌避
シート等、特殊の方法に頼らざるを得ない。また、殺虫
後のその害虫死体の残留も二次的に問題になり、最終的
には人力により取り除かねばならない。この観点より、
忌避剤の利用は大いに効果のあるものであるが、前述の
既知の害虫忌避剤は、その効力、持続性及び人畜毒性の
面からもう一歩力不足で、全く新規の物質の開発が臨ま
れていた。また、主に戸外の通信回路の機器に危害を及
ぼすアリの被害も現代情報化社会への被害が大きく、そ
の対策がのぞまれていたが、本発明はこの困難な課題を
解決したものである。In addition, with the recent development of office automation, large numbers of individuals can be found in various OA equipment such as computers and pumps, which are perfect habitats due to the atmosphere inside the building and the appropriate temperature inside the equipment. began to exhibit interference with the equipment's functionality. Furthermore, many different types of box-shaped food and beverage vending machines are now being installed due to their simplicity, and cockroaches have started to appear in these machines as well. To prevent this, when using insecticides, special methods such as spraying into closed equipment must be used, such as poison baits and insect repellent sheets. In addition, the remaining pest corpses after killing the insects becomes a secondary problem, and ultimately must be removed manually. From this point of view,
Although the use of repellents is highly effective, the known pest repellents mentioned above are still lacking in terms of efficacy, sustainability, and toxicity to humans and animals, and the development of completely new substances is currently underway. Ta. In addition, the damage caused by ants, which mainly harm outdoor communication circuit equipment, has caused great damage to the modern information society, and countermeasures have been needed.The present invention solves this difficult problem. be.
本発明の害虫忌避組成物は、フェニルエーテル又はベン
ジルエーテルを含有することを特徴とする。The pest repellent composition of the present invention is characterized by containing phenyl ether or benzyl ether.
ソシて、フェニルエーテル又はベンジルエーテルは、そ
の目的に応じて高級脂肪酸及びその誘導体、アミノ酸誘
導体、糖誘導体、天然ワックス及び合成樹脂と、相溶固
形物、皮膜、包接、カプセル化物及びその賦型物、又は
天然又は合成繊維組成物等に含浸され賦型物化したもの
として使用できる。Depending on the purpose, phenyl ether or benzyl ether can be used as a compatible solid substance, film, clathrate, encapsulated product, or shaped product with higher fatty acids and their derivatives, amino acid derivatives, sugar derivatives, natural waxes, and synthetic resins. It can be used as a material, or as a material impregnated with a natural or synthetic fiber composition and shaped.
本発明は、フェニルエーテル又はベンジルエーテルは害
虫、特にゴキブリ及びアリに忌避作用が抜群であること
を見出したことに基づくものである。The present invention is based on the discovery that phenyl ether or benzyl ether has an outstanding repellent effect on pests, especially cockroaches and ants.
アリは、膜翅目、ツチバチ上科、アリ科に属する昆虫で
、女工を中心とした家族的社会生活をしている。全世界
で約1万種、本邦には300種以上生息しているが、居
住環境の周辺では日本南部で約30種、北部で10〜2
0種を見ることができる。刺すアリは、ハリアリ亜科に
属する種類で、代表的な種類はオオハリーアリである。Ants are insects that belong to the order Hymenoptera, the superfamily Trichidae, and the family Formicidae, and they live a family-like social life centered on female workers. There are about 10,000 species worldwide, and more than 300 species in Japan, but around the residential environment, there are about 30 species in southern Japan and 10 to 2 species in northern Japan.
0 species can be seen. Stinging ants are a species belonging to the subfamily Chiliidae, and the representative species is the carpenter ant.
大部分のアリは刺さないが足部より蟻酸を含む化学物質
を放出する。Most ants do not sting, but they release chemicals including formic acid from their legs.
家屋周辺に見られるアリは、アミメアリ、イエヒメアリ
、オオハアリ、ヤマアリ等があり、樹幹の腐朽部、枯枝
中に営巣するトビイロケアリ、ハリブトアリ、オオアリ
、クロトゲアリ等は屋外電信機器例えば接続端子函内に
営巣し、屡々通信被覆部を食害し通信機能を麻痺させ一
大損害を与える場合がある。その駆除方法は、家屋周辺
のアリは、防疫用有機燐素、カーバメート系の殺虫剤を
散布して防除できるが、室内ではピレスロイド系化合物
のエアゾールで駆除する。屋内への侵入防止には、家屋
の内外を点検して木材の腐敗している箇所を補修したり
防腐剤を塗布して巣を作られないようにする。プロポク
スル粒剤などを家の周囲に帯状に配置したり、周辺の土
地を深く耕したり、また、アリの食べ物となる甘露を補
給、周辺の植物に寄生しているアブラムシを駆除するの
も効果がある。また、樹幹の腐朽部等に営巣するものは
ゴキブリと同様通信機器の密閉系内への施薬、通信機器
の多種類の材質に安全なもので殺蟻力のあるものより毒
性の面からも安全な忌避素材によるのが好ましい。この
観点よりすれば、本発明のフェニルエーテル又はベンジ
ルエーテルを主成分とした組成物を用いるのが最も効果
的である。Ants found around houses include red-eared ants, house ants, carpenter ants, and wood ants, and ants such as brown ants, carpenter ants, carpenter ants, and black-spined ants, which nest in decaying tree trunks and dead branches, nest inside outdoor telegraph equipment, such as connection terminal boxes. This often damages the communication covering, paralyzing communication functions and causing major damage. Ants can be exterminated around houses by spraying organic phosphorus and carbamate insecticides for epidemic prevention, but indoors they can be exterminated using aerosols containing pyrethroid compounds. To prevent them from entering your home, inspect the inside and outside of your home and repair any rotting wood or apply preservatives to prevent them from building nests. It is also effective to place propoxur granules in a strip around the house, deeply plow the surrounding land, supply honeydew, which is food for ants, and exterminate aphids parasitic on surrounding plants. be. In addition, similar to cockroaches, those that nest in rotten parts of tree trunks should be treated with chemicals that are safe for the sealed systems of communication equipment, and are safe for the many types of materials used in communication equipment, and are safer from the standpoint of toxicity than those that have anticidal properties. It is preferable to use repellent materials. From this point of view, it is most effective to use a composition containing the phenyl ether or benzyl ether of the present invention as a main component.
かかる機能性素材としてフェニルエーテル及びベンジル
エーテルは全く新規のものである。Phenyl ether and benzyl ether are completely new as such functional materials.
この2物質の毒性値は、ラット経口急性毒性LI)so
は3370mg/kg及び2500mg/kgで医薬用
殺虫剤で低毒性とされるフェニトロチオン(MEPジメ
チル−4−ニトロ−m−トリル・フォスホロチオネート
)のL Dio1376mg/kg に比較して非常に
毒性の少ない安全なものである。The toxicity values of these two substances are rat oral acute toxicity LI) so
is 3370mg/kg and 2500mg/kg, which is very toxic compared to L Dio1376mg/kg of fenitrothion (MEP dimethyl-4-nitro-m-tolyl phosphorothionate), which is considered to be a low toxicity pharmaceutical insecticide. It is less safe.
以下これらエーテルにつき記述する。These ethers will be described below.
1、 フェニルエーテル(別名1.1’−オキシビス
ベンゼン、ジエフェニルエーテル、ジフェニルオキシド
) (c@H5)20、分子量170.20. 屈
折率n a’1.5795、芳香液体、比重(20°)
1.075(liq)、融点28°、沸点259 ”
、引火点115 °、水に不溶、アルコール、ベンゼ
ン、氷酢酸に溶ける。1. Phenyl ether (also known as 1.1'-oxybisbenzene, diephenyl ether, diphenyl oxide) (c@H5) 20, molecular weight 170.20. Refractive index n a'1.5795, aromatic liquid, specific gravity (20°)
1.075 (liq), melting point 28°, boiling point 259”
, flash point 115°, insoluble in water, soluble in alcohol, benzene, and glacial acetic acid.
フェノールのアルカリ金属塩とモノクロルベンゼンと加
熱して合成され、石鹸香料、熱溶媒、溶剤として利用さ
れ、ゼラニウム様の香気がある。It is synthesized by heating an alkali metal salt of phenol and monochlorobenzene, and is used as a soap fragrance, heat solvent, and solvent, and has a geranium-like fragrance.
2、 ベンジルエーテル(別名1.1’−1”オキシ
ビス(メチレン)〕ビス〔ベンゼン〕、ジベンジルエー
テル、ジベンジルオキシド) (C@ H5CH2
)20、分子量198.25. 屈折率naJ、56
01、芳香液体、比重(20°)1.0014、沸点2
89 ’ 、引火点135°、水に不溶、アルコール、
ベンゼン。2. Benzyl ether (also known as 1.1'-1" oxybis(methylene)]bis[benzene], dibenzyl ether, dibenzyl oxide) (C@H5CH2
) 20, molecular weight 198.25. Refractive index naJ, 56
01, aromatic liquid, specific gravity (20°) 1.0014, boiling point 2
89', flash point 135°, insoluble in water, alcohol,
benzene.
氷酢酸に溶ける。ベンズアルデヒドをコバルト四カルボ
ニルを用いて還元し製造されるが、塩化ベンジルをアル
カリ加水分解によりベンジルアルコールを製造する際、
副生物としても得られる。湿気にやや不安定で、一部ベ
ンズアルデヒドを生成することもあり、生成物も忌避作
用はあるが、分解を防止することは容易である。このベ
ンジルエーテルは石鹸香料、香料溶剤、染色キャリア、
ニトロセルロース可塑剤として利用される。Soluble in glacial acetic acid. It is produced by reducing benzaldehyde with cobalt tetracarbonyl, but when benzyl alcohol is produced by alkaline hydrolysis of benzyl chloride,
It can also be obtained as a by-product. It is somewhat unstable to moisture and may produce some benzaldehyde, and although the product also has a repellent effect, it is easy to prevent decomposition. This benzyl ether is used as soap fragrance, fragrance solvent, dye carrier,
Used as a nitrocellulose plasticizer.
このフェニルエーテル又はベンジルエーテルを害虫忌避
剤として実際利用する製剤化にはその目的に合った剤型
とすることができる。即ち白灯油等に溶かした液剤(油
剤)を始め、粉剤、水和剤。When preparing a formulation for actually using this phenyl ether or benzyl ether as an insect repellent, it can be made into a dosage form suitable for the purpose. In other words, liquids (oils) dissolved in white kerosene, powders, and wettable powders.
粒剤、乳剤、エアゾール、燻蒸剤、粘着剤等に常法によ
り容易に製剤される。しかし、本成分が常温で液体であ
るため固形化するため又成分放出速度を律速させるため
、高級脂肪酸及びその誘導固形化合物と相溶させたり、
アミノ酸誘導体、糖誘導体、例えばベンジリデンソルビ
トール、天然又は合成ワックスと相溶又は無機硫酸塩類
粉末と混溶してゲル化、固形化したり、ゼラチン、アラ
ビアゴム、合成樹脂、ガラス膜等でマイクロカプセル化
して律速する。また、これら忌避機能性素材を天然又は
合成m維シート、テープ等に含浸固定化することができ
るのである。It can be easily formulated into granules, emulsions, aerosols, fumigants, adhesives, etc. by conventional methods. However, since this component is liquid at room temperature, it solidifies, and in order to limit the rate of release of the component, it is mixed with higher fatty acids and their derived solid compounds,
Amino acid derivatives and sugar derivatives, such as benzylidene sorbitol, are compatible with natural or synthetic waxes or mixed with inorganic sulfate powder to gel and solidify, or microencapsulated with gelatin, gum arabic, synthetic resin, glass membrane, etc. Set the speed. Furthermore, these repellent functional materials can be impregnated and fixed into natural or synthetic m-fiber sheets, tapes, and the like.
本発明ノフェニルエーテル又はペンシルエーテルを忌a
成分とした組成物は、各種害虫に対しての忌避力は嗅覚
による嗅覚忌避剤(Olfactory repell
ent) としての作用が大で味覚忌避剤(Gust
at。The nophenyl ether or pencil ether of the present invention is prohibited.
The composition as an ingredient has repellent power against various pests as an olfactory repellent (Olfactory repellent).
ENT) has a strong effect as a taste repellent (Gust).
at.
ry repellent) としての効果もあるが
、前者による作用の方が対象物の最初の噛害を防止し得
る特徴がある。かかる特色のある作用機能の利用は非常
に広範囲に有効な忌避器材を提供でき、人畜又は農林作
物、工芸品1通信機器、OA機器等に利用できる。ry repellent), but the former action has the advantage of being able to prevent the initial biting of the object. Utilization of such unique functions can provide a very wide range of effective repellent equipment, which can be used for humans, livestock, agricultural and forestry crops, crafts, communication equipment, OA equipment, etc.
また、本発明の忌避剤は、先に本発明者らが開発し、特
願昭63−124763号明細書において開示したテル
ペノイドモノマー及びそのオリゴマーと併用すれば、有
害動物忌避剤としてさらに有効な広範なものを対象とす
る忌避組成物を得ることができる。なお、フェニルエー
テルについては、本発明者らは先にネズミ忌避剤として
有効であることを見出し、これを、特願昭63−176
164号明細書において開示したが、本発明に右いてベ
ンジルエーテルと共に一般害虫特にゴキブリ及びアリに
対し強力な忌避作用があることを見出したものである。Furthermore, the repellent of the present invention can be used in combination with the terpenoid monomer and its oligomer, which were previously developed by the present inventors and disclosed in Japanese Patent Application No. 63-124763, to provide a more effective wide range of harmful animal repellents. It is possible to obtain a repellent composition that is directed against. Regarding phenyl ether, the present inventors had previously discovered that it was effective as a rat repellent, and this was published in a patent application filed in 1983-176.
Although it was disclosed in the specification of No. 164, it has been found that, together with benzyl ether, it has a strong repellent action against general pests, especially cockroaches and ants.
また、CA4521405(1942)、濃化1? 1
077(1941)。Also, CA4521405 (1942), Concentration 1? 1
077 (1941).
1827(1942) には、フェニルエーテル及び
ベンジルエーテルはその燃焼ガスの状態でネックイイエ
カ(Culex quinquefasciatus
5ay)について落下致死力があることが発表されてい
るが、その忌避力については何ら述べられていない。1827 (1942), phenyl ether and benzyl ether were found in the form of their combustion gases in the Culex quinquefasciatus.
5ay) has been announced to have lethal fall power, but nothing has been said about its repellency.
また、J、 Econ、 E+N、60379(195
7)には、フェニルエーテルについてチチュウ力イミバ
エの誘引フェロモンであるトリメトルア誘引剤への効力
増強剤として検討されているが、その効果は殆どないよ
うである。Also, J, Econ, E+N, 60379 (195
7), phenyl ether has been investigated as an effect enhancer for the Trimetolua attractant, which is a pheromone that attracts the fruit fly, but it seems to have little effect.
実施例 l
フェニルエーテル80%、マイクロワックス20%を約
80°に加温して相溶させ、厚さ1IIlfll、幅5
cmの不織布テープ(木綿30%、ポリエステル繊維
20%、ナイロン1m 1450%)に含浸ローラーに
かけ室温にて放冷してフェニルエーテル65%含有忌避
テープを得る。Example l 80% phenyl ether and 20% microwax were heated to about 80° to make them compatible, and the thickness was 1IIlfll and the width was 5.
cm of nonwoven fabric tape (30% cotton, 20% polyester fiber, 1 m 1450% nylon) was applied with an impregnated roller and allowed to cool at room temperature to obtain a repellent tape containing 65% phenyl ether.
実施例 2
実施例1のフェニルエーテルの代わりにベンジルエーテ
ルを用いて同様にしてベンジルエーテル65%含有忌避
テープを得る。Example 2 A repellent tape containing 65% benzyl ether is obtained in the same manner as in Example 1, using benzyl ether instead of phenyl ether.
実施例 3
フェニルエーテル40部、ポリアクリル系水性乳化重合
液(固形分50%、アニオン型pH4〜5020部を混
合分散させ、アルミニウムシートに広げ、50°に通風
乾燥させ、フェニルエーテル40%含有厚さ約1鮒のフ
ェニルエーテル40%含有忌避シートを得た。Example 3 40 parts of phenyl ether and 40 parts of polyacrylic aqueous emulsion polymerization liquid (solid content 50%, anionic pH 4 to 5020 parts) were mixed and dispersed, spread on an aluminum sheet, and dried with ventilation at 50° to form a mixture containing 40% phenyl ether. A repellent sheet containing 40% phenyl ether was obtained for about 1 carp.
実施例 4
実施例3のフェニルエーテルの代わりにベンジルエーテ
ルを用いて同様にしてベンジルエーテル40%含有シー
トを得た。Example 4 A sheet containing 40% benzyl ether was obtained in the same manner as in Example 3, using benzyl ether instead of phenyl ether.
以下、本発明の害虫忌避剤実施例の効果について次の試
験例にて説明する。Hereinafter, the effects of the pest repellent examples of the present invention will be explained in the following test examples.
試験例 l ゴキブリ忌避試験
供試虫:チャバネゴキブリ (a出糸、 F−78代)
成虫
方法:セルター忌避試験法によった。即ち試験ポット(
φ15cm、 h 18cm)の内壁に合わせ、厚紙で
コの字型セルターを作りその内側に実施例1及び2の忌
避テープをそれぞれ側面に両面テープで張りつけたもの
を試験セルターとした。対照には無処理不織布を張りつ
けたものを試験ポア)の中に入れ、雌雄各々lO匹を成
虫し、常法により飼育した。経時毎セルター内に隠れる
虫数を計数した。Test example l Cockroach repellent test test insect: German cockroach (a-thread, F-78 generation)
Adult method: According to the Selter repellent test method. i.e. test pot (
A test selter was prepared by making a U-shaped selter made of cardboard and pasting the repellent tapes of Examples 1 and 2 on the sides with double-sided tape to the inside of the selter. As a control, an untreated nonwoven fabric was placed in the test pore), and 10 male and female adults were grown and reared in a conventional manner. The number of insects hiding in the selter was counted over time.
その試験効果を第1表に示す。The test effects are shown in Table 1.
第1表 なお、試験中約50日経過後は次代生体が発生する。Table 1 Note that a next generation organism is generated after about 50 days during the test.
試験例 2 アリ忌避試験
供試虫:クロトゲアリ、沖縄産(電話線接続端子函より
採取)
方法ニガラスポット(φ15cm、 h 18cm)の
内部を厚紙で2室に分画し、1室に検体(φ3.5cm
の切取りシート)を置き、他の1室にも自由に選択侵入
できるようにし、供試虫20匹を放飼した。10分毎各
室に定置する束数を調査し、これを60分間にわたり調
査した。その試験結果を第2表に示す。Test example 2 Ant repellent test test insect: black-spotted ant, from Okinawa (collected from a telephone line connection terminal box) Method: Divide the inside of a Nigara pot (φ15 cm, height 18 cm) into two chambers with cardboard, and place the specimen in one chamber ( φ3.5cm
A cut-out sheet) was placed, and 20 test insects were released into the other room, allowing them to freely selectively enter the room. The number of bundles placed in each room was checked every 10 minutes, and this was checked over a period of 60 minutes. The test results are shown in Table 2.
なお、忌避率は(l−試験区数/対照区数)X100で
算出した。In addition, the repellency rate was calculated by (l - number of test plots/number of control plots) x 100.
第2表
害をその機能を低下させることなく、人畜に低毒性で且
つ工業製品材料として経済的に製造し得るフェニルエー
テル又はペンジルエーテルヲ素材トした害虫忌避剤を製
造可能としたものである。かかる見地から見れば、本発
明の効果は甚だ大なるものと言える。To make it possible to produce a pest repellent made of phenyl ether or pendyl ether, which has low toxicity to humans and livestock and can be economically produced as a material for industrial products without reducing its function. From this point of view, the effects of the present invention can be said to be enormous.
Claims (1)
害虫忌避組成物。 2、請求項1の記載において、フェニルエーテル又はベ
ンジルエーテルが高級脂肪酸及びその誘導体、アミノ酸
誘導体、糖誘導体、天然ワックス及び合成樹脂と、相溶
固形物、皮膜、包接、カプセル化物及びその賦型物、又
は天然又は合成繊維組成物等に含浸され賦型物化した害
虫忌避組成物。[Claims] 1. A pest repellent composition containing phenyl ether or benzyl ether. 2. In the description of claim 1, phenyl ether or benzyl ether is compatible with higher fatty acids and their derivatives, amino acid derivatives, sugar derivatives, natural waxes, and synthetic resins, and solids, films, inclusions, encapsulates, and shapes thereof. A pest repellent composition impregnated with a natural or synthetic fiber composition or the like to form a molded product.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27314489A JPH03133904A (en) | 1989-10-19 | 1989-10-19 | Insect pest-repellent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27314489A JPH03133904A (en) | 1989-10-19 | 1989-10-19 | Insect pest-repellent |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03133904A true JPH03133904A (en) | 1991-06-07 |
Family
ID=17523732
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP27314489A Pending JPH03133904A (en) | 1989-10-19 | 1989-10-19 | Insect pest-repellent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03133904A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03271203A (en) * | 1990-03-20 | 1991-12-03 | Mikasa Kagaku Kogyo Kk | Injurious animal-repelling composition |
JP2008274461A (en) * | 2007-04-26 | 2008-11-13 | Asahi Kasei Corp | Optically controlled nonwoven fabric and composite material |
JP2016034972A (en) * | 2013-02-28 | 2016-03-17 | 大日本除蟲菊株式会社 | Insecticide with aroma, insect repellent device with aroma, and production method of insecticide with aroma |
-
1989
- 1989-10-19 JP JP27314489A patent/JPH03133904A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03271203A (en) * | 1990-03-20 | 1991-12-03 | Mikasa Kagaku Kogyo Kk | Injurious animal-repelling composition |
JP2008274461A (en) * | 2007-04-26 | 2008-11-13 | Asahi Kasei Corp | Optically controlled nonwoven fabric and composite material |
JP2016034972A (en) * | 2013-02-28 | 2016-03-17 | 大日本除蟲菊株式会社 | Insecticide with aroma, insect repellent device with aroma, and production method of insecticide with aroma |
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