JPH0262805A - Termite-controllling agent for treating wooden portion - Google Patents
Termite-controllling agent for treating wooden portionInfo
- Publication number
- JPH0262805A JPH0262805A JP63212748A JP21274888A JPH0262805A JP H0262805 A JPH0262805 A JP H0262805A JP 63212748 A JP63212748 A JP 63212748A JP 21274888 A JP21274888 A JP 21274888A JP H0262805 A JPH0262805 A JP H0262805A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- termite
- agent
- test
- controlling agent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 36
- 241000256602 Isoptera Species 0.000 claims abstract description 30
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 6
- DPWOZBNWORICSR-UHFFFAOYSA-N 1-(2-hydroxyethoxy)-7-(6-propyl-1,3-benzodioxol-5-yl)heptan-2-ol Chemical compound C1=C(CCCCCC(O)COCCO)C(CCC)=CC2=C1OCO2 DPWOZBNWORICSR-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000002023 wood Substances 0.000 claims description 23
- -1 Dimethyl (4-ethoxyphenyl) Chemical group 0.000 claims description 7
- 239000012752 auxiliary agent Substances 0.000 claims 1
- UIDUKLCLJMXFEO-UHFFFAOYSA-N propylsilane Chemical compound CCC[SiH3] UIDUKLCLJMXFEO-UHFFFAOYSA-N 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 17
- 150000001875 compounds Chemical class 0.000 abstract description 11
- 239000000203 mixture Substances 0.000 abstract description 7
- 239000002917 insecticide Substances 0.000 abstract description 3
- 244000144972 livestock Species 0.000 abstract description 3
- 239000002689 soil Substances 0.000 abstract description 3
- 239000005667 attractant Substances 0.000 abstract description 2
- 230000031902 chemoattractant activity Effects 0.000 abstract description 2
- 238000009472 formulation Methods 0.000 abstract description 2
- 230000002421 anti-septic effect Effects 0.000 abstract 1
- 238000013329 compounding Methods 0.000 abstract 1
- HPYNBECUCCGGPA-UHFFFAOYSA-N silafluofen Chemical compound C1=CC(OCC)=CC=C1[Si](C)(C)CCCC1=CC=C(F)C(OC=2C=CC=CC=2)=C1 HPYNBECUCCGGPA-UHFFFAOYSA-N 0.000 abstract 1
- 229940126062 Compound A Drugs 0.000 description 27
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 27
- 238000012360 testing method Methods 0.000 description 27
- 230000000749 insecticidal effect Effects 0.000 description 9
- 239000003921 oil Substances 0.000 description 9
- 229960005235 piperonyl butoxide Drugs 0.000 description 9
- 239000002728 pyrethroid Substances 0.000 description 9
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 8
- 241000607479 Yersinia pestis Species 0.000 description 7
- 239000000077 insect repellent Substances 0.000 description 6
- 230000002195 synergetic effect Effects 0.000 description 6
- 241000238631 Hexapoda Species 0.000 description 5
- 239000003814 drug Substances 0.000 description 5
- 229940079593 drug Drugs 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 5
- 239000003350 kerosene Substances 0.000 description 5
- 239000004570 mortar (masonry) Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 239000005944 Chlorpyrifos Substances 0.000 description 4
- 241000255925 Diptera Species 0.000 description 4
- SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- ATROHALUCMTWTB-OWBHPGMISA-N phoxim Chemical compound CCOP(=S)(OCC)O\N=C(\C#N)C1=CC=CC=C1 ATROHALUCMTWTB-OWBHPGMISA-N 0.000 description 3
- 229950001664 phoxim Drugs 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 230000004580 weight loss Effects 0.000 description 3
- 241000254173 Coleoptera Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Chemical compound C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 description 2
- 239000003517 fume Substances 0.000 description 2
- 230000002262 irrigation Effects 0.000 description 2
- 238000003973 irrigation Methods 0.000 description 2
- 231100000053 low toxicity Toxicity 0.000 description 2
- 239000011120 plywood Substances 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 1
- HOLHYSJJBXSLMV-UHFFFAOYSA-N 2,6-dichlorophenol Chemical compound OC1=C(Cl)C=CC=C1Cl HOLHYSJJBXSLMV-UHFFFAOYSA-N 0.000 description 1
- LDXJRKWFNNFDSA-UHFFFAOYSA-N 2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical group C1CN(CC2=NNN=C21)CC(=O)N3CCN(CC3)C4=CN=C(N=C4)NCC5=CC(=CC=C5)OC(F)(F)F LDXJRKWFNNFDSA-UHFFFAOYSA-N 0.000 description 1
- YEVQZPWSVWZAOB-UHFFFAOYSA-N 2-(bromomethyl)-1-iodo-4-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=C(I)C(CBr)=C1 YEVQZPWSVWZAOB-UHFFFAOYSA-N 0.000 description 1
- WZFUQSJFWNHZHM-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 WZFUQSJFWNHZHM-UHFFFAOYSA-N 0.000 description 1
- WYVVKGNFXHOCQV-UHFFFAOYSA-N 3-iodoprop-2-yn-1-yl butylcarbamate Chemical compound CCCCNC(=O)OCC#CI WYVVKGNFXHOCQV-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241001124076 Aphididae Species 0.000 description 1
- 241001674044 Blattodea Species 0.000 description 1
- 241001609213 Carassius carassius Species 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229920000858 Cyclodextrin Polymers 0.000 description 1
- 241001466042 Fulgoromorpha Species 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 241000257303 Hymenoptera Species 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 241000257226 Muscidae Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 244000184734 Pyrus japonica Species 0.000 description 1
- 241000866500 Reticulitermes speratus Species 0.000 description 1
- 244000000231 Sesamum indicum Species 0.000 description 1
- 235000003434 Sesamum indicum Nutrition 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 241000256248 Spodoptera Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 230000001887 anti-feedant effect Effects 0.000 description 1
- 229940027983 antiseptic and disinfectant quaternary ammonium compound Drugs 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 235000012216 bentonite Nutrition 0.000 description 1
- 229960000686 benzalkonium chloride Drugs 0.000 description 1
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- BIWJNBZANLAXMG-YQELWRJZSA-N chloordaan Chemical compound ClC1=C(Cl)[C@@]2(Cl)C3CC(Cl)C(Cl)C3[C@]1(Cl)C2(Cl)Cl BIWJNBZANLAXMG-YQELWRJZSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229940125898 compound 5 Drugs 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- XQUXKZZNEFRCAW-UHFFFAOYSA-N fenpropathrin Chemical compound CC1(C)C(C)(C)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 XQUXKZZNEFRCAW-UHFFFAOYSA-N 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 238000003898 horticulture Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- OCWMFVJKFWXKNZ-UHFFFAOYSA-L lead(2+);oxygen(2-);sulfate Chemical compound [O-2].[O-2].[O-2].[Pb+2].[Pb+2].[Pb+2].[Pb+2].[O-]S([O-])(=O)=O OCWMFVJKFWXKNZ-UHFFFAOYSA-L 0.000 description 1
- 230000001665 lethal effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000003992 organochlorine insecticide Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- ZPORCTAUIXXZAI-UHFFFAOYSA-N phenyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC1=CC=CC=C1 ZPORCTAUIXXZAI-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000005846 sugar alcohols Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 210000000115 thoracic cavity Anatomy 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はジメチル(4−エトキシフェニiv>(3−(
3−フェノキシ−4−フルオロフエニlv)プロピル)
シラン(以下化合物Aと称す)を含有することを特徴と
する木部処理用臼アリ防除剤に関する。Detailed Description of the Invention [Industrial Field of Application] The present invention relates to dimethyl (4-ethoxyphenyiv>(3-(
3-phenoxy-4-fluorophenyl (lv)propyl)
This invention relates to a mortar ant control agent for wood treatment, which is characterized by containing silane (hereinafter referred to as compound A).
近年、木材を食害する害虫、例えば白アリ。 In recent years, pests that damage wood, such as termites, have become increasingly popular.
フナクイムシ、ヒラタキクイムシ等の被害が問題となっ
ているが、これらの害虫に食害されないために、あらか
じめ用材や床下土壌に防虫剤を処理する方法が従来より
行われ、この目的のために殺虫、防虫成分としてクロル
デン、デイlレドリン等の有機塩素系殺虫剤が使われて
きた。Damage caused by crucian carp beetles, flatback beetles, etc. has become a problem, but in order to prevent damage from these pests, the conventional method has been to treat lumber and sub-soil with insect repellents in advance. Organochlorine insecticides such as chlordane and dayledrin have been used as ingredients.
しかしながら、これらの殺虫、防虫成分はいずれも残留
性、毒性、刺激性、環境汚染などの点で問題があり、昨
年使用が禁止され、これらに替わるものとして、クロル
ピリホス。However, these insecticidal and repellent ingredients all have problems in terms of persistence, toxicity, irritation, and environmental pollution, and their use was banned last year, and chlorpyrifos was introduced as an alternative.
ホキシムなどの有機リン剤が最近上布された。Organophosphorus agents such as phoxim have recently been introduced.
上記有機リン系白アリ防除剤は環境中で分解されやすい
ため長期間にわたる白アリ防除効果が乏しく、また人畜
に対する安全性の点で問題が多いという欠点があり、低
毒性の新し・い白アリ防除剤の開発が切望されている。The organophosphorus termite control agents mentioned above have the disadvantage of being easily decomposed in the environment, resulting in poor termite control effects over a long period of time, and also having many safety issues for humans and livestock. There is a strong need for the development of an ant control agent.
〔問題点を解決するための手段及び作用〕本発明者らは
、低毒性を特徴とするピレスロこの種の目的に使用でき
るものを長年研究してきたが、その結果、クロμデン、
デイ〃ドリンより殺虫性、残効性において優れた化合物
とし゛て化合物Aを見い出した。[Means and effects for solving the problems] The present inventors have been researching for many years on pyrethros that can be used for this type of purpose, which are characterized by low toxicity, and as a result, we found that cloden,
Compound A was found to be a compound superior to deidrin in terms of insecticidal properties and residual efficacy.
化合物Aは、特にりン翅目の害虫、アブラムシ類、ウン
カ類等に高い殺虫活性を有するため農園芸用分野で実用
化が検討されているが、し−、′
直翅目の害虫に対して低活性であることからと考えられ
ていた。Compound A is being considered for practical use in the field of agriculture and horticulture, as it has high insecticidal activity against insect pests of the order Phosphoroptera, aphids, planthoppers, etc.; This was thought to be due to its low activity.
した時、白アリ防除剤の殺虫、防虫成分の評価としては
基礎殺虫効力試験のみでは不適切であると考え、種々の
化合物について実用的な木部処理試験を行ったところ化
合物Aが高い食害防止効果を示すことが明らかとなった
。At that time, we thought that basic insecticidal efficacy tests alone were inappropriate for evaluating the insecticidal and insect repellent ingredients of termite control agents, and when we conducted practical wood treatment tests on various compounds, we found that Compound A had a high rate of preventing insect damage. It has become clear that it is effective.
化合物Aはピレスロイド系薬剤としての特長である昆虫
に対する速効性、温血動物に対して低毒性という長所を
もつと同時に非常にすぐれ九′残効性を有している。Compound A has the advantages of rapid action against insects and low toxicity against warm-blooded animals, which are the characteristics of a pyrethroid drug, and at the same time it has an extremely good residual effect.
更に本発明者らは、化合物Aが有機塩素系膜、享剤や有
機リン剤と比べると高価な殺虫剤であることを鑑み、コ
ストダウンを図る目的で化合物Aとピレスロイド用共力
剤の混合による効果を白アリについて鋭意検討した結果
、サイネビリン500、オクタクロロジグロビルエーテ
ル′、MGKL264、M a K −5−fJ 26
、セサミのピレスロイド用共力剤はいずれも効果なく、
白アリに対しては特異的に化合物Aと〔3,4−(メチ
レンジオキシ)−6−ブロピルベンジμ〕ブチルジエチ
レングフイコールエーテル〔以下ピベロニルプトキサイ
ドと称す〕の組み合わせのみが著しい効果を示すことを
見いだし本発明を完成した。Furthermore, in view of the fact that Compound A is an expensive insecticide compared to organochlorine membranes, recreational chemicals, and organophosphorus agents, the present inventors developed a mixture of Compound A and a pyrethroid synergist for the purpose of reducing costs. As a result of intensive studies on the effects of cynevirin 500, octachlorodiglobyl ether', MGKL264, M a K -5-fJ 26 on termites,
, Sesame's pyrethroid synergists are all ineffective,
Only the combination of Compound A and [3,4-(methylenedioxy)-6-propylbendiμ]butyldiethyleneguficol ether [hereinafter referred to as piveronyl ptoxide] is particularly effective against termites. The present invention was completed based on the discovery that the following is true.
これまでは、例えばハエ、蚊などに対する試験結果から
、各種ピレスロイド用共力剤は化合物Aとの組み合わせ
では多少の差があっても同様に共力効果を示すものと考
えられていただけに、白アリに対する特有の現象は従来
の知見からは全く予期しえないものである。Previously, it was thought that various pyrethroid synergists would exhibit similar synergistic effects when combined with Compound A, even if there were slight differences, based on test results on flies, mosquitoes, etc. The phenomenon peculiar to ants is completely unexpected from conventional knowledge.
この結果、化合物Aの配合量を減らしても高い殺虫、防
虫効果を得ることができ、・コスト面での実用的メリッ
トは極めて大きい。As a result, high insecticidal and insect repellent effects can be obtained even if the amount of compound A is reduced, and the practical advantage in terms of cost is extremely large.
本発明で用いる化合物Aは次式(I)で示され分子中に
ケイ素原子を含有コしている。Compound A used in the present invention is represented by the following formula (I) and contains a silicon atom in the molecule.
木部処理用白アリ防除剤には殺虫、防虫成分として化合
物Aを0.01〜90重量%含有することができ、ピペ
ロニA/2)キサイドと混合する場合、高い共力効果を
奏する化合物Aとピベロニルブトキサイドとの混合比は
3:1〜1:20(好ましくはl:1〜1:10)が適
当である。The termite control agent for wood treatment can contain 0.01 to 90% by weight of Compound A as an insecticidal and insect repellent component, and when mixed with Piperoni A/2)oxide, Compound A exhibits a high synergistic effect. and piveronyl butoxide in a suitable mixing ratio of 3:1 to 1:20 (preferably 1:1 to 1:10).
また、殺虫、防虫効果をより効率的に発揮させるために
白アリ誘引剤を適宜配合してもよい。更に、本発明の木
部処理用白アリ防除剤に、側光ばクロルピリホス、ホキ
シム、ピリダフェンチオンなどの有機リン剤、バーメス
リン、フェンバレレート1、フェンプロパスリンなどの
ピレスロイド剤あるいはトリプロビルイ、ソシアヌレー
ト、カーバメート剤などの他の殺虫剤、また、次に示す
ような種々のタイプの防腐剤
0CCx系化合物−OCA 、 COBなど0ハロフ工
ノール系化合物−ベンタクロ〜フェニルラウレート、p
−プロモー2.6−ジクロルフェノールなど
0ヨ一ドプロパルギル系化合物−xp−1000゜3−
ヨード−2−プロピニルブチルカーバメ−トなど
O第4級アンモニウム化合物およびアミン塩−。In addition, a termite attractant may be appropriately added in order to exhibit insecticidal and insect repellent effects more efficiently. Furthermore, the termite control agent for wood treatment of the present invention may include organic phosphorus agents such as chlorpyrifos, phoxim, and pyridafenthione, pyrethroid agents such as vermethrin, fenvalerate 1, and fenpropathrin, or triprobyl, socyanurate, and carbamate agents. Other insecticides, as well as various types of preservatives, such as CCx-based compounds - OCA, COB, etc. - halofonicol-based compounds - bentacro to phenyllaurate, p
-Promo 2.6-Dichlorophenol and other 0 iodopropargyl compounds -xp-1000°3-
O quaternary ammonium compounds and amine salts such as iodo-2-propynylbutyl carbamate.
ベンザルコニウムクロリド、ジアルキルジメチルアンモ
ニウムクロリドなど
o有機スズ化合物、−ビス−(n−)リプチルスズ)オ
キシド、トリプチルスズテレフタレートナoその他−・
ナフテン酸亜鉛、キシリゲンアルミニウム塩など
を適宜混合して有用な多目的組成物を得ることもできる
。Benzalkonium chloride, dialkyldimethylammonium chloride, etc.Organotin compounds, -bis-(n-)liptyltin) oxide, triptyltin terephthalate, etc.
A useful multipurpose composition can also be obtained by appropriately mixing zinc naphthenate, xyligen aluminum salt, and the like.
本発明木部処理用臼アリ防除剤の剤型としては、防除剤
の性状、使用目的により、油剤、乳剤、水利剤、水溶剤
、粉剤、エアゾール剤など種々可能であるが油剤が一般
的に使用される。いずれの製剤も常法に従って調製する
ことができ、固体担体としては粘土類(カオリン、ベン
トナイト類など)、タルク類などの微粉末ないし粉状物
があげられる。液体担体としては、水、アルコ−/L’
類、芳香族炭化水素類(例えばトルエン、キシレンなど
)、脂肪族炭化水素類(例えばケロシン、灯油など)、
エステル類、ニトリル類などが使用できる。次に界面活
性剤としては、アルキル硫酸エステμ類、アルキpスμ
ホン酸塩、アルキルアリールスルホン酸塩、ポリエチレ
ングリコールエーテル類、多価アルコールエステル類な
どがあげられる。その他適宜、カゼイン、ゼラチン、で
んぷん粉、CMC、ホリヒニルアルコールなどの固着剤
や分散剤が使用される。また、本発明で使用される化合
物Aをマイクロカプセル化あるいはサイクロデキストリ
ン包接化することにより、更に化学的安定性を増し残効
性を高めることができる。The formulation of the mortar ant control agent for treating wood of the present invention may be various depending on the properties of the control agent and the purpose of use, such as oil, emulsion, irrigation agent, water solvent, powder, or aerosol, but oil is generally used. used. Any of the preparations can be prepared according to a conventional method, and solid carriers include fine powders or powders such as clays (kaolin, bentonites, etc.), talcs, and the like. Liquid carriers include water, alcohol/L'
aromatic hydrocarbons (e.g. toluene, xylene, etc.), aliphatic hydrocarbons (e.g. kerosene, kerosene, etc.),
Esters, nitriles, etc. can be used. Next, as surfactants, alkyl sulfate ester μ, alkyl ps μ
Examples include phonates, alkylarylsulfonates, polyethylene glycol ethers, and polyhydric alcohol esters. In addition, fixing agents and dispersing agents such as casein, gelatin, starch powder, CMC, and polyhinyl alcohol are used as appropriate. Further, by microencapsulating or cyclodextrin inclusion of Compound A used in the present invention, chemical stability can be further increased and residual efficacy can be enhanced.
一方、化合物Aとピベロニルプトキサイドの混合物につ
いても上記と同様の効果が得られる。On the other hand, the same effect as above can be obtained with a mixture of Compound A and piveronyl ptoxide.
本発明の木部処理用臼アリ防除剤の適用方法としては、
従来の方法例えば家屋木部に乳剤、油剤、水利剤、粉剤
などを散布あるいは泡沫施用したり、木材や合板などに
塗布や加圧注入する方法や、更に白アリ防除用ベイト剤
あるいは着色ペイントやニス等に含浸させて白アリ予防
コーティング剤として施用することも可能である。The method of applying the mortar ant control agent for wood treatment of the present invention is as follows:
Conventional methods include spraying or foaming emulsions, oils, irrigation agents, powders, etc. on the wood of houses, coating or pressure injection on wood and plywood, and methods such as termite control baits, colored paints, etc. It is also possible to impregnate varnish or the like and apply it as a termite preventive coating.
以下本発明の有用性を一層明確にするため、実施例及び
試験例について説明するが本発明がこれらのみに限定さ
れるものでないことはもちろんである。EXAMPLES In order to further clarify the usefulness of the present invention, Examples and Test Examples will be described below, but it goes without saying that the present invention is not limited to these.
実施例1
化合物A0.2部、及び工y−10000,8部を煙霧
灯油に溶解して全体を100部として油剤を得る。Example 1 An oil solution was obtained by dissolving 0.2 parts of Compound A and 8 parts of Y-10000 in fume kerosene to make the total 100 parts.
実施例2
化合物AO01部、ピベロニルブトキサイド0.4部、
及び3−ヨード−2−プロビニルブチルカーバメート0
.フ部をプロピレングライコールモノメチルエーテル5
部及び煙霧灯油に溶解して全体を100部として油剤を
得る。防虫加工する木材をこの油剤に浸漬するか、この
油剤を表面に散布又は塗布する。Example 2 01 part of compound AO, 0.4 part of piveronyl butoxide,
and 3-iodo-2-provinylbutylcarbamate 0
.. Propylene glycol monomethyl ether 5
1 part and dissolved in fume kerosene to make a total of 100 parts to obtain an oil solution. The wood to be insect-proofed is dipped in this oil, or the oil is sprayed or applied on the surface.
実施例3
化合物A2部、ピベロニルプトキサイド10部にツルポ
ー、/L/5M−200(東邦化学登録商標名)5部、
キシロ−/I/20部、白灯油63部を加え、これらを
よくかく拌混合溶解して乳剤を得る。Example 3 2 parts of compound A, 10 parts of piveronyl ptoxide, 5 parts of Tsurupo, /L/5M-200 (registered trademark of Toho Chemical),
Add 20 parts of Xylo-/I and 63 parts of white kerosene, stir well, mix and dissolve, and obtain an emulsion.
この乳剤を水で20倍に希釈17、その液に木材を浸漬
するか、表面に塗布又は散布する。This emulsion is diluted 20 times with water (17), and the wood is immersed in the solution or applied or sprayed on the surface.
合板製造に使用するフェノール系尿素、メラミン系接着
剤97.5部にこの乳剤2.5部を加えてよく混合し使
用する。2.5 parts of this emulsion is added to 97.5 parts of a phenolic urea and melamine adhesive used for manufacturing plywood, mixed well, and used.
実施例4
化合物A1部、ピベロニpブトキサイド5部をトリオク
チルホスフェート25部に溶解し、塩化ビニμ原料樹脂
50部、三塩基性硫酸鉛2.5部、およびりpり16.
5部を加え、よく混合して電線被覆用の塩化ビニルコン
パウンドを得る。Example 4 1 part of Compound A and 5 parts of Piveroni p-butoxide were dissolved in 25 parts of trioctyl phosphate, 50 parts of vinyl chloride μ raw material resin, 2.5 parts of tribasic lead sulfate, and 16.
Add 5 parts and mix well to obtain a vinyl chloride compound for covering electric wires.
試験例1
(木部処理試@)
(社)日本しろあり対策協会規格に基づき、供試薬剤の
所定1度の油剤を木片(I X I X2cm)に11
0g/yIの割合で塗布し、2週間風乾後そのそれぞれ
を試験片としだ。Test example 1 (Wood treatment test @) Based on the standards of the Japan Whitening Prevention Association, a prescribed 1 degree oil of the test agent was applied to a piece of wood (I x I x 2 cm) for 11 hours.
It was applied at a rate of 0 g/yI, and after air-drying for 2 weeks, each was used as a test piece.
次に゛これらの試験片を同一のイエシロアリの巣箱内に
それぞれ各1片ずつ設置し、3週間後の食害による重量
減少率及び蟻道の状況を観察した。Next, one piece of each of these test pieces was placed in the same nest box for termites, and the rate of weight loss due to feeding damage and the condition of the ant trail were observed after 3 weeks.
なお表において、0〜マで示される加害度合は生じた蟻
道数の程度であり、蟻道数なしく0)から蟻道数著しい
(V)までの段階を示す。In the table, the degree of damage indicated by 0 to M is the degree of the number of ant tracks that occurred, and indicates the stage from 0 (no number of ant tracks) to (V) with a significant number of ant tracks.
(局部施用接触試験)
イエシロアリの背部に供試薬剤の各種濃度のアセトン溶
液をマイクロシリンジにて局部施用し、24時間後の死
生率から接触による薬剤の基礎効力を調べた。(Topical application contact test) Acetone solutions of various concentrations of the test drug were locally applied to the backs of domestic termites using a microsyringe, and the basic efficacy of the drug upon contact was determined from the mortality rate after 24 hours.
ハエ、蚊、ゴキブリなど衛生害虫駆除では薬剤との接触
あるいは摂取によるノックダウン効果と引きつづいて起
こる致死効果が最も重要であるが、白アリ駆除の場合は
衛生害虫駆除の場合とは全く異なる。When exterminating sanitary pests such as flies, mosquitoes, and cockroaches, the most important factors are the knockdown effect and subsequent lethal effect caused by contact with or ingestion of chemicals, but exterminating termites is completely different from sanitary pest extermination.
すなわち、白アリは共生原生動物の助けでセルロースを
消化しこれの維持のために排出物を食べあう習性から集
団生活を営んでおり、白アリを一匹や数匹殺虫しても防
除にはならない。また、白アリは排出物や粘土などを利
用して巣や蟻道を加工し主に地中で生活するため衛生害
虫のように人目につくことはまれで、白アリの巣ごと全
滅させるかあるいは白アリの食害から木材や建築物を保
護することが白アリ防除剤の究極の役目といえる。従っ
て、局部施用接触試験は効力評価の目やすにはなるとし
てもそれだけでは意味をなさず、供試薬剤処理した木片
を白アリ生息環境下に設置し食害状況を観察する方法(
試験例1の木部処理試験)が社日本しろあり対策協会の
防蟻効力試験法として定められている。In other words, termites live in groups by digesting cellulose with the help of symbiotic protozoa and eating each other's excreta to maintain this quality, so killing one or several termites is not effective in controlling them. It won't happen. In addition, termites use excrement and clay to create nests and ant trails, and live mainly underground, so they rarely attract attention like sanitary pests, so it is difficult to wipe out the entire termite nest. In other words, the ultimate role of termite control agents is to protect wood and buildings from termite damage. Therefore, although the local application contact test may serve as a guide for efficacy evaluation, it alone is meaningless; instead, a method of placing wood chips treated with the test chemical in a termite habitat and observing the feeding damage (
The wood treatment test in Test Example 1) has been established as the anti-termite effectiveness test method by the Japanese White Ant Countermeasures Association.
試験の結果、化合物Aは局部施用接触試験では対照の他
のピレスロイド剤(&2〜4)及び有機リン剤(A5;
ホキシム)に比べて効力が低かったが、木部処理試験で
は最も高い食害防止効果を示し、白アリ防除剤の殺虫、
防虫成分としての有用性が明らかとなった。The test results showed that Compound A was superior to other pyrethroid agents (&2-4) and organophosphorus agent (A5;
Although the efficacy was lower than that of phoxim), it showed the highest anti-feeding effect in the wood treatment test, and was effective as a termite control agent.
Its usefulness as an insect repellent ingredient has been revealed.
(0日本しろあり対策協会規格では重量減少率が3%以
下の場合合格とされている。)一方、他のピレスロイド
剤であるバーメスリンは、局部施用接触試験では高い活
性を示したものの食害防止効果は化合物Aよりかなり劣
った。この理由の一つとして、バーメスリンが環境中で
分解を受けやすい点があげられ、白アリ防除剤の開発に
あたっては、実用的な総合評価が必要であることを示し
ている。(According to the Japan White Ant Countermeasures Association standards, a weight loss rate of 3% or less is considered acceptable.) On the other hand, another pyrethroid, vermethrin, showed high activity in a local application contact test, but had no effect on preventing feeding damage. It was considerably inferior to Compound A. One of the reasons for this is that vermethrin is susceptible to decomposition in the environment, indicating the need for practical comprehensive evaluation when developing termite control agents.
試験例2
化合物Aに種々のピレスロイド用共力剤を3倍量添加し
た供試薬剤のアセトン溶液をマイクロシリンジにてイエ
シロアリの背部、イエバエ成虫の胸部背板及びハスモン
ヨトウの背部に施用し48時間後の死生率から共力剤に
よる殺虫力の共力効果をみたところ次の通りであった。Test Example 2 An acetone solution of a test drug prepared by adding three times the amount of various pyrethroid synergists to Compound A was applied with a microsyringe to the backs of house termites, the thoracic back plate of adult house flies, and the backs of Spodoptera japonica, and 48 hours later. The synergistic effect of the insecticidal power of the synergist was examined from the mortality rate of the insects, and the results were as follows.
々お、対照薬剤として有機リン剤のクロルピリホスを用
いた。Chlorpyrifos, an organophosphorus agent, was used as a control agent.
試験の結果、化合物Aとピレスロイド用共力剤のうちの
ピベロニルプトキサイドの組み合わせが、イエシロアリ
に対してのみ特異的に高μ共力効果を示すことが明らか
となった。As a result of the test, it was revealed that the combination of Compound A and piveronyl ptoxide, which is a pyrethroid synergist, exhibits a high-μ synergistic effect specifically against the domestic termite.
一方、対照薬剤のクロルピリホスの場合、共力剤の種類
や供試昆虫の種類による共力効果の差異はあまり認めら
れなかった。On the other hand, in the case of the control drug chlorpyrifos, little difference in the synergistic effect was observed depending on the type of synergist or the type of insect tested.
ヤマトシロアリについても同様の傾向が得られた。A similar trend was observed for Yamato termites.
試験例3
試験例2においてビベロニルブトキサイドのイエシロア
リに対する特異的共力効果が明らかとなったので試験例
1に準じ、下記の供試油剤を用いて木部処理試験を行つ
たところ以下の如くであった。Test Example 3 In Test Example 2, the specific synergistic effect of biveronyl butoxide against the Japanese termite was clarified, so a wood treatment test was conducted using the following test oil according to Test Example 1, and the following results were obtained. It was like that.
試験の結果、木部処理試験においても化合物Aにピベロ
ニルブトキサイドを加えることによって食害防止効果が
著しく増強し、ピベロニルプトキサイドが化合物Aの濃
度低減化に有効であることが確認された。なお、化合物
Aとピベロニルブトキサイドの混合比は重量減少率3%
以下が合格という基準から判断すると化合物Aの濃度が
0.1%の場合l:1〜1:2、化合物Aの濃度が0.
05%の場合1:1〜1:10で十分な効果が得られた
。また、化合物Aとピベロニルブトキサイドの混合比が
1:20のものではピベロニルブトキサイドの添加量に
比例するほどの効力アップはなかった。As a result of the test, the addition of piveronyl butoxide to Compound A significantly enhanced the feeding damage prevention effect in the wood treatment test, indicating that piveronyl butoxide is effective in reducing the concentration of Compound A. confirmed. The mixing ratio of compound A and piveronyl butoxide is a weight loss rate of 3%.
Judging from the following criteria for passing, if the concentration of compound A is 0.1%, l:1 to 1:2;
In the case of 0.05%, a sufficient effect was obtained with a ratio of 1:1 to 1:10. Furthermore, when the mixing ratio of Compound A and piveronyl butoxide was 1:20, the efficacy did not increase to a degree proportional to the amount of piveronyl butoxide added.
本発明の木部処理用臼アリ防除剤は、従来の有機リン系
木部処理用臼アリ防除剤に比べ、人畜に対する安全性、
土壌中の安定性及び白アリ防除効果にすぐれ、極めて有
用な防除薬剤を提供するものである。The mortar ant control agent for wood treatment of the present invention is safer for humans and livestock than conventional organophosphorus-based mortar ant control agents for wood treatment.
The present invention provides an extremely useful pest control agent with excellent stability in soil and termite control effects.
Claims (2)
フェノキシ−4−フルオロフェニル)プロピル}シラン
を含有することを特徴とする木部処理用白アリ防除剤。(1) Dimethyl (4-ethoxyphenyl) {3-(3-
A termite control agent for treating wood, characterized by containing phenoxy-4-fluorophenyl)propylsilane.
ベンジル〕プチルジエチレングライコールエーテルを助
剤として含有することを特徴とする特許請求の範囲第(
1)項記載の木部処理用白アリ防除剤。(2) Claim No. 1, characterized in that it contains [3,4-(methylenedioxy)-6-propylbenzyl]butyl diethylene glycol ether as an auxiliary agent.
The termite control agent for wood treatment described in section 1).
Priority Applications (1)
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---|---|---|---|
JP63212748A JP2810384B2 (en) | 1988-08-26 | 1988-08-26 | Termite control agent for wood treatment |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63212748A JP2810384B2 (en) | 1988-08-26 | 1988-08-26 | Termite control agent for wood treatment |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0262805A true JPH0262805A (en) | 1990-03-02 |
JP2810384B2 JP2810384B2 (en) | 1998-10-15 |
Family
ID=16627769
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EP0669191A1 (en) * | 1994-02-24 | 1995-08-30 | Timberquest International (Pty) Ltd | A biocide composition for the treatment of timber |
JP2008536894A (en) * | 2005-04-22 | 2008-09-11 | エンデュラ ソシエタ ペル アチオニ | New biologically active formulations |
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JPS62108885A (en) * | 1985-11-08 | 1987-05-20 | Mitsui Toatsu Chem Inc | Organosilicon compound, production thereof and insecticide containing said compound |
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EP0667097A1 (en) * | 1994-02-02 | 1995-08-16 | Hoechst Schering AgrEvo GmbH | Formulation and method for control of social insects |
EP0669191A1 (en) * | 1994-02-24 | 1995-08-30 | Timberquest International (Pty) Ltd | A biocide composition for the treatment of timber |
JP2008536894A (en) * | 2005-04-22 | 2008-09-11 | エンデュラ ソシエタ ペル アチオニ | New biologically active formulations |
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