JP2020138950A - Termite controlling stomach poisoning agent and method for producing the same - Google Patents
Termite controlling stomach poisoning agent and method for producing the same Download PDFInfo
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Abstract
Description
本発明は、木質材料を用いたシロアリ防除用食毒剤およびその防除方法に関する。 The present invention relates to a termite control toxicant using a wood-based material and a method for controlling the termites.
シロアリは、木造建造物、木製家具・調度品、紙製美術品等に食害をもたらす。そこで、シロアリ用の防蟻成分を木材などの木質材料に処理した食毒剤をシロアリに摂取させて防除する方法が知られている(特許文献1)。 Termites cause feeding damage to wooden structures, wooden furniture / furniture, and paper works of art. Therefore, there is known a method of controlling termites by ingesting termites with a poisoning agent obtained by treating a wood-based material such as wood with an anti-termite component (Patent Document 1).
本発明は、シロアリに対しより効果のある食毒剤、およびその製造方法を提供することである。 The present invention is to provide a more effective phagocytosis against termites and a method for producing the same.
本発明者らは上記課題を解決するために鋭意検討を行った結果、木材表面にキチン合成阻害剤を一定量含有するシロアリ防除用食毒剤により、シロアリを効果的に防除することを見出し、本発明に至った。 As a result of diligent studies to solve the above problems, the present inventors have found that termites can be effectively controlled by a termite control toxicant containing a certain amount of a chitin synthesis inhibitor on the wood surface. The present invention has been reached.
すなわち、本発明の構成は以下のとおりである。
〔1〕木片の表面100cm2あたりキチン合成阻害剤を3.2〜64mg含有するシロアリ防除用食毒剤。
〔2〕木片がスギ類またはマツ類であることを特徴とする上記シロアリ防除用食毒剤
〔3〕木片がスギ類であって、該木片の表面積の20%以上が白太であることを特徴とする上記シロアリ防除用食毒剤。
〔4〕上記シロアリ防除用食毒剤を用いて、シロアリを防除する方法。
〔5〕表面積の20%以上が白太である木片に対しキチン合成阻害剤を処理することを特徴とするシロアリ防除用食毒剤の製造方法。
That is, the configuration of the present invention is as follows.
[1] A termite control toxicant containing 3.2 to 64 mg of a chitin synthesis inhibitor per 100 cm 2 of the surface of a piece of wood.
[2] The termite control poisoning agent characterized in that the wood piece is a cedar or a pine [3] The wood piece is a cedar, and 20% or more of the surface area of the wood piece is white. The above-mentioned termite control poisoning agent.
[4] A method for controlling termites by using the above-mentioned termite control poisoning agent.
[5] A method for producing a termite control toxicant, which comprises treating a piece of wood whose surface area is 20% or more white with a chitin synthesis inhibitor.
本発明のシロアリ防除用食毒剤を用いれば、シロアリを効率よく防除することができる。また本発明のシロアリ防除用食毒剤を効率よく製造することができる。 By using the termite control poisoning agent of the present invention, termites can be efficiently controlled. Further, the termite control poisoning agent of the present invention can be efficiently produced.
本発明のシロアリ防除用食毒剤に使用されるキチン合成阻害剤とは、昆虫のキチン質の合成を阻害することで脱皮を阻害するものである。前記キチン合成阻害剤としては、以下の式に示す化合物を用いることが好ましい。
式(1)
〔式中、R1はハロゲンまたは水素を表わし、R2はハロゲンを表わし、Xは水素、ハロゲン、アルキル、ハロアルキル、アルコキシまたはハロアルコキシをわし、mは1、2または3の数を表わし、Xが複数個あるときは、夫々のXは同一または相異なることができ、Yは水素、ハロゲン、アルキル、ハロアルキル、アルコキシまたはハロアルコキシを表わし、nは1、2、3または4の数を表わし、Yが複数個あるときは、夫々のYは同一または相異なることができ、R3は水素、ハロゲン、アルキル、ハロアルキル、アルコキシ、ハロアルコキシ、ハロアルコキシハロアルキルまたはO-Rを表わし、ここにRはハロアルキルまたは式(2)
の置換されたフェニル基を表わし、ここにZは水素、ハロゲン、アルキル、ハロアルキル、アルコキシまたはハロアルコキシを表わし、そしてpは1、2、3または4の数を表わし、Zが複数個あるときは、夫々のZは同一または相異なることができ、R4はハロゲンまたはハロアルキルを表わし、そしてQはCHまたはNを表わす。〕で示される化合物。
これら有効成分のうち、キチン合成阻害性活性成分が好ましく、さらに好ましくは、
式(3)
〔式中、R'1はフッ素、塩素または水素を表わし、R'2はフッ素または塩素を表わし、X'が水素を表し、m'が3の数を表し、Y'が水素、フッ素、塩素またはCF3を表わし、nは1、2、3または4の数を表わし、Y'が複数個あるときは、夫々のY'は同一または相異なることができ、R'3は水素、フッ素、塩素、CF3または式O-R'で示される基を表わし、ここにR'は炭素原子1〜3個並びに塩素、フッ素原子1〜7個を有するハロアルキルまたはハロアルコキシハロアルキルを表わすか、あるいは
R'は式(4)
の置換されたフェニル基を表わし、ここにZ'は水素、フッ素または塩素を表わし、
pは1、2、3または4の数を表わし、ここに置換基Z'が複数個あるときは、夫々のZ'は同一または相異なることができ、R'4は炭素原子1〜6個並びにフッ素及び/または塩素原子1〜13個を有するハロアキルを表わし、そしてQはCHまたはNを表わす。〕で示される化合物である。
よりさらに好ましくは、上記の式(1)および(2)の化合物の中で、R1、R2、R3、R4、X、Y、n、m、p、Q、Zがそれぞれ以下に示す組成、数字である化合物〔1〕から〔8〕であり、化合物〔3〕が特に好ましい。
化合物〔1〕は、式(1)のR1はフッ素であり、R2はフッ素であり、Xは水素(m=3)であり、Yは水素(n=4)であり、R3は塩素である。
化合物〔2〕は、式(1)のR1はフッ素であり、R2はフッ素であり、Xは水素(m=3)であり、Yは水素(n=1)、フッ素(n=1)、塩素(n=2)であり、(2−フッ素、3−塩素、5−塩素)であり、R3はフッ素である。
化合物〔3〕は、式(1)のR1はフッ素であり、R2はフッ素であり、Xは水素(m=3)であり、Yは水素(n=1)、塩素(n=1)、CF3(n=2)であり、(2−塩素、3−CF3、5−CF3)であり、R3は水素である。
化合物〔4〕は、式(1)のR1はフッ素であり、R2はフッ素であり、Xは水素(m=3)であり、Yは水素(n=2)、塩素(n=2)であり、(3−塩素、5−塩素)であり、R3はOCF2CHF2である。
化合物〔5〕は、式(1)のR1はフッ素であり、R2はフッ素であり、Xは水素(m=3)であり、Yは水素(n=2)、塩素(n=2)であり、(2−塩素、5−塩素)であり、R3はOCF2CHFCF3である。
化合物〔6〕は、式(1)のR1はフッ素であり、R2はフッ素であり、Xは水素(m=3)であり、Yは水素(n=1)、フッ素(n=1)、塩素(n=2)であり、(2−フッ素、3−塩素、5−塩素)であり、R3はOCF2CHFCF3である。
化合物〔7〕は、式(1)のR1はフッ素であり、R2はフッ素であり、Xは水素(m=3)であり、Yは水素(n=3)、塩素(n=1)であり、(3−塩素)であり、R3はOCF2CHFOCF3である。
化合物〔8〕は、式(1)のR1はフッ素であり、R2はフッ素であり、Xは水素(m=3)であり、Yは水素(n=2)、塩素(n=2)であり、(3−塩素、5−塩素)であり、R3はOーRであり、Rは式(2)の置換されたフェニル基のZは水素(p=2)、塩素(p=1)であり、(3−塩素)であり、R4はCF3であり、QはNである。
The chitin synthesis inhibitor used in the termite control toxicant of the present invention inhibits molting by inhibiting the synthesis of chitin in insects. As the chitin synthesis inhibitor, it is preferable to use a compound represented by the following formula.
Equation (1)
[In the formula, R 1 represents halogen or hydrogen, R 2 represents halogen, X represents hydrogen, halogen, alkyl, haloalkyl, alkoxy or haloalkoxy, m represents the number 1, 2 or 3, and X. When there is more than one, each X can be the same or different, Y represents hydrogen, halogen, alkyl, haloalkyl, alkoxy or haloalkoxy, n represents the number 1, 2, 3 or 4 When there are multiple Y's, each Y can be the same or different, where R 3 stands for hydrogen, halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, haloalkoxyhaloalkyl or O-R, where R stands for Haloalkane or formula (2)
Represents the substituted phenyl group of, where Z represents hydrogen, halogen, alkyl, haloalkyl, alkoxy or haloalkoxy, and p represents the number 1, 2, 3 or 4, when there are multiple Zs. , Each Z can be the same or different, R 4 represents a halogen or haloalkyl, and Q represents CH or N. ] The compound indicated by.
Of these active ingredients, chitin synthesis inhibitory active ingredients are preferable, and more preferably
Equation (3)
Wherein, R '1 represents fluorine, chlorine or hydrogen, R' 2 represents a fluorine or chlorine, X 'is hydrogen, m' represents a number of 3, Y 'is hydrogen, fluorine, chlorine or represents CF 3, n represents a number 1, 2, 3 or 4, Y 'when there is a plurality, the respective Y' can be identical or different, R '3 represents hydrogen, fluorine, Represents a group represented by chlorine, CF 3 or formula OR', where R'represents a haloalkyl or haloalkoxyhaloalkyl having 1-3 carbon atoms and 1-7 chlorine, fluorine atoms, or
R'is equation (4)
Represents the substituted phenyl group of, where Z'represents hydrogen, fluorine or chlorine,
p represents the number 1, 2, 3 or 4, wherein the substituent Z 'when there is a plurality, the respective Z' may be the same or different, R '4 is 1 to 6 carbon atoms Also represents a haloacyl having 1 to 13 fluorine and / or chlorine atoms, and Q represents CH or N. ] Is a compound indicated by.
Even more preferably, among the compounds of the above formulas (1) and (2), R1 , R2 , R3 , R4 , X, Y, n, m, p, Q and Z are as follows. Compounds [1] to [8] have the compositions and numbers shown, and compound [3] is particularly preferable.
In compound [1], R 1 of the formula (1) is fluorine, R 2 is fluorine, X is hydrogen (m = 3), Y is hydrogen (n = 4), and R 3 is. It is chlorine.
In the compound [2], R 1 of the formula (1) is fluorine, R 2 is fluorine, X is hydrogen (m = 3), Y is hydrogen (n = 1), and fluorine (n = 1). ), Chlorine (n = 2), (2-fluorine, 3-chlorine, 5-chlorine), and R 3 is fluorine.
In compound [3], R 1 of the formula (1) is fluorine, R 2 is fluorine, X is hydrogen (m = 3), Y is hydrogen (n = 1), and chlorine (n = 1). ), a CF3 (n = 2), a (2-chlorine, 3-CF3,5-CF 3) , R 3 is hydrogen.
In compound [4], R 1 of the formula (1) is fluorine, R 2 is fluorine, X is hydrogen (m = 3), Y is hydrogen (n = 2), and chlorine (n = 2). ), (3-Chlorine, 5-chlorine), and R 3 is OCF 2 CHF 2 .
In compound [5], R 1 of the formula (1) is fluorine, R 2 is fluorine, X is hydrogen (m = 3), Y is hydrogen (n = 2), and chlorine (n = 2). ), (2-Chlorine, 5-chlorine), and R 3 is OCF 2 CHFCF 3 .
In the compound [6], R 1 of the formula (1) is fluorine, R 2 is fluorine, X is hydrogen (m = 3), Y is hydrogen (n = 1), and fluorine (n = 1). ), Chlorine (n = 2), (2-fluorine, 3-chlorine, 5-chlorine), and R 3 is OCF 2 CHFCF 3 .
In compound [7], R 1 of the formula (1) is fluorine, R 2 is fluorine, X is hydrogen (m = 3), Y is hydrogen (n = 3), and chlorine (n = 1). ), (3-Chlorine), and R 3 is OCF 2 CHFOCF 3 .
In the compound [8], R 1 of the formula (1) is fluorine, R 2 is fluorine, X is hydrogen (m = 3), Y is hydrogen (n = 2), and chlorine (n = 2). ), (3-Chlorine, 5-Chlorine), R 3 is OR, R is hydrogen (p = 2), chlorine (p = 2), Z of the substituted phenyl group of the formula (2). = 1), (3-chlorine), R 4 is CF 3 , and Q is N.
本発明のシロアリ防除用食毒剤は、前記キチン合成阻害剤を木片の表面100cm2あたりに3.2〜64mg含有するように処理される。 The termite control toxicant of the present invention is treated so as to contain 3.2 to 64 mg of the chitin synthesis inhibitor per 100 cm 2 of the surface of a piece of wood.
本発明のシロアリ防除用食毒剤に使用される木片は、スギ類、マツ類が挙げられる。前記スギ類としては、セッカンスギ、ヒマラヤスギなどが挙げられ、前記マツ類としては、アカマツ、クロマツ、エゾマツ、カラマツ、ベニマツ、スプルースなどが挙げられる。これらのうち、スギ類で、かつ木片の表面積の20%以上が白太であることが好ましい。なお白太は辺材と呼ばれることもある。木材の表面積の白太の割合が本範囲内にあると、所定量のキチン合成阻害剤を含有するシロアリ防除用食毒剤を安定して製造することが可能となる。 Examples of wood chips used in the termite control poisoning agent of the present invention include cedars and pine trees. Examples of the Japanese cedar include Japanese cedar and cedar, and examples of the Japanese cedar include Japanese red pine, Japanese black pine, spruce pine, larch, Beni pine, and spruce. Of these, it is preferable that cedars and 20% or more of the surface area of the piece of wood is white. Shirata is sometimes called sapwood. When the proportion of white thick on the surface area of wood is within this range, it becomes possible to stably produce a termite control toxicant containing a predetermined amount of chitin synthesis inhibitor.
前記木片の形状としては、板状、円盤状、球状、杭状、円柱状、多角柱状、球、楕円球など、使用する場面に応じて適宜決定すればよい。また、前記木片の大きさも、本発明のシロアリ防除用食毒剤を設置する場所に応じて適宜決定すればよい。 The shape of the piece of wood may be appropriately determined depending on the situation in which it is used, such as a plate shape, a disk shape, a spherical shape, a pile shape, a columnar shape, a polygonal columnar shape, a sphere, or an elliptical sphere. Further, the size of the piece of wood may be appropriately determined according to the place where the termite control poisoning agent of the present invention is installed.
本発明のシロアリ防除用食毒剤には、シプロコナゾール、ヘキサコナゾール、テブコナゾール、プロピコナゾール、F−69などのアゾール系化合物、IPBCなどの有機ヨウ素系化合物などの防腐剤、TBZなどのベンゾイミダゾール系、有機ヨウ素系としてIF−1000やIPBCなどの有機ヨウ素系化合物、TCMTBなどのベンゾチアゾール系化合物、MBCなどのチオシアネート系化合物などの防カビ剤を必要に応じて1種または2種以上使用することができる。 The toxic agent for controlling white ants of the present invention includes azole compounds such as cyproconazole, hexaconazole, tebuconazole, propiconazole and F-69, preservatives such as organic iodine compounds such as IPBC, TBZ and the like. One or more antifungal agents such as benzimidazole-based, organic iodine-based compounds such as IF-1000 and IPBC, benzothiazole-based compounds such as TCMTB, and thiocyanate-based compounds such as MBC as required. Can be used.
本発明のシロアリ防除用食毒剤は、例えば、キチン合成阻害剤を含有する乳剤の水希釈液に木片を浸漬する、あるいは木片の表面に前記水希釈液を塗布することにより製造することができる。 The termite control poisoning agent of the present invention can be produced, for example, by immersing a piece of wood in a water-diluted solution of an emulsion containing a chitin synthesis inhibitor, or by applying the water-diluted solution to the surface of the piece of wood. ..
本発明のシロアリ防除用食毒剤が防除対象とするシロアリは、ヤマトシロアリ、イエシロアリ、アメリカカンザイシロアリ、ダイコクシロアリ、タイワンシロアリ、コウシュンシロアリ、サツマシロアリ、ナカジマシロアリ)、カタンシロアリ、コダマシロアリ、クシモトシロアリ、オオシロアリ、コウシュウイエシロアリ、アマミシロアリ、キアシシロアリ、カンモンシロアリ、タカサゴシロアリ等のシロアリ類が挙げられる。 The termites to be controlled by the termite control toxicant of the present invention are termites such as Yamato termites, termites, American termites, Daikoku termites, Taiwan termites, Koshun termites, Satsuma termites, Nakajima termites), termites, termites, and termites. Examples thereof include termites such as termites, termites, termites, termites, termites, termites, termites, termites, and termites.
本発明のシロアリ防除用食毒剤は、例えば、家屋の周囲に、1〜5mの間隔で前記シロアリ防除用食毒剤を設置することでシロアリの防除が可能となる。また、家の水回りや玄関周囲部のコーナー部分にも前記と同じ間隔で設置してもよい。 The termite control poisoning agent of the present invention can control termites by, for example, installing the termite control poisoning agent around a house at intervals of 1 to 5 m. Further, it may be installed at the same intervals as described above in the water area of the house or in the corner portion around the entrance.
以下に、実施例により本発明を具体的に説明するが、本発明はこれらの実施例によって限定されるものではない。 Hereinafter, the present invention will be specifically described with reference to Examples, but the present invention is not limited to these Examples.
(実施例1)
段落8の式(4)の化合物〔3〕1部をブチルジグリコール81重量部に溶解し、ニューカルゲンCP80(竹本油脂株式会社)18重量部を加え、よく攪拌混合して、1%乳剤を得た。そして、乳剤10.4gを白太50%のスギの木片(大きさ10×6.5×1cm)の表面に塗布、風乾して、100cm2あたりのキチン合成阻害剤の付着量が64mgであるシロアリ防除用食毒剤を得た。
(Example 1)
1 part of the compound [3] of the formula (4) of paragraph 8 is dissolved in 81 parts by weight of butyl diglycol, 18 parts by weight of New Calgen CP80 (Takemoto Oil & Fats Co., Ltd.) is added, and the mixture is thoroughly stirred and mixed to prepare a 1% emulsion. Obtained. Then, 10.4 g of the emulsion is applied to the surface of a 50% termite wood piece (size 10 x 6.5 x 1 cm) and air-dried, and the amount of the chitin synthesis inhibitor attached per 100 cm 2 is 64 mg. Obtained a termite control toxicant.
(実施例2)
実施例1において、乳剤の処理量を乳剤5.2gに変更し、100cm2あたりのキチン合成阻害剤の付着量が32mgであるシロアリ防除用食毒剤を得た。
(Example 2)
In Example 1, the treated amount of the emulsion was changed to 5.2 g of the emulsion to obtain a termite control toxicant having an adhering amount of the chitin synthesis inhibitor per 100 cm 2 of 32 mg.
(実施例3)
実施例1において、乳剤の濃度を0.1%乳剤、処理量を5.2gに変更した、100cm2あたりのキチン合成阻害剤の付着量が3.2mgであるシロアリ防除用食毒剤を得た。
(Example 3)
In Example 1, a termite control toxicant was obtained in which the concentration of the emulsion was changed to 0.1% emulsion and the treatment amount was changed to 5.2 g, and the amount of the chitin synthesis inhibitor attached per 100 cm 2 was 3.2 mg. It was.
(比較例1)
実施例1において、乳剤の濃度を0.05%、処理量を5.2gに変更した、100cm2あたりのキチン合成阻害剤の付着量が1.6mgであるシロアリ防除用食毒剤を得た。
(Comparative Example 1)
In Example 1, a termite control venom was obtained in which the concentration of the emulsion was changed to 0.05% and the treatment amount was changed to 5.2 g, and the amount of the chitin synthesis inhibitor attached per 100 cm 2 was 1.6 mg. ..
(比較例2)
実施例1において、乳剤の濃度を0.01%、処理量を5.2gに変更した、100cm2あたりのキチン合成阻害剤の付着量が0.16mgであるシロアリ防除用食毒剤を得た。
(Comparative Example 2)
In Example 1, a termite control venom was obtained in which the concentration of the emulsion was changed to 0.01% and the treatment amount was changed to 5.2 g, and the amount of the chitin synthesis inhibitor attached per 100 cm 2 was 0.16 mg. ..
(試験例1)
透明プラスチック容器(13×21×3cm)内に、実施例1で得られた木片1枚と、9.5×13cmの紙に水を含ませて配置し、供試虫(イエシロアリ職蟻)300頭を放虫した。6週間後に供試虫の生死の状況、及び食害度を観察した。前記の木片を再度使用して同様の試験を繰り返し実施し、以下に示す判定基準で評価した。
〔生死の状況の判定基準〕
++:およそ70%以上生存
+:およそ50%以上生存
±:およそ1%以上50%未満生存
−:生存なし
〔食害度の判定基準(目視)〕
++:食害あり
+:一部食害あり
±:わずかに食害あり
−:食害なし
実施例2、実施例3、比較例1および比較例2のシロアリ防除用食毒剤についても上記試験を行った。表1に結果を示す。
(Test Example 1)
In a transparent plastic container (13 x 21 x 3 cm), one piece of wood obtained in Example 1 and a piece of paper of 9.5 x 13 cm soaked in water were placed, and a test insect (Formosan subterranean termite) 300 I released my head. After 6 weeks, the life and death status of the test insects and the degree of feeding damage were observed. The same test was repeated using the above-mentioned piece of wood again and evaluated according to the criteria shown below.
[Criteria for life / death situation]
++: Survival of about 70% or more +: Survival of about 50% or more ±: Survival of about 1% or more and less than 50%-: No survival [Criteria for determining the degree of feeding damage (visual)]
++: With feeding damage +: With some feeding damage ±: Slightly with feeding damage −: No feeding damage The above tests were also conducted on the termite control poisoning agents of Example 2, Example 3, Comparative Example 1 and Comparative Example 2. The results are shown in Table 1.
〔表1〕
[Table 1]
初回の試験では、比較例1および比較例2の毒餌剤においてもシロアリを防除することはできるが、実施例に比べ毒餌剤に食害が多いために、2回目の試験では、充分なシロアリ防除効果が得られなかった。 In the first test, termites can be controlled even with the poison bait agents of Comparative Example 1 and Comparative Example 2, but since the poison bait agent has more feeding damage than the examples, a sufficient termite control effect is obtained in the second test. Was not obtained.
(試験例2)
スギ木片(大きさ10×6.5×1cm)を、白太の表面積比率で20%未満、20%以上50%未満、50%以上の3種を準備した。実施例1で作成した乳剤の10倍希釈液に木片を5分間浸漬後、風乾した。浸漬前後の重量から木片の薬剤含有量を算出した。前記試験を5反復した結果を表2に示す。
(Test Example 2)
Three types of Japanese cedar wood pieces (size 10 x 6.5 x 1 cm) were prepared in terms of the surface area ratio of white thick, less than 20%, 20% or more and less than 50%, and 50% or more. A piece of wood was immersed in a 10-fold diluted solution of the emulsion prepared in Example 1 for 5 minutes and then air-dried. The chemical content of the piece of wood was calculated from the weight before and after immersion. Table 2 shows the results of repeating the test 5 times.
〔表2〕
[Table 2]
白太の表面積比率が20%未満では薬剤含有量にばらつきがみられ、薬剤含有量が3.2mgを下回る毒餌剤が作成された。 When the surface area ratio of white thick was less than 20%, the drug content varied, and a poison bait with a drug content of less than 3.2 mg was prepared.
(設置例)
実施例2のシロアリ防除用食毒剤を家屋の床下底面のコーナー部に配置した。また、コーナー部に設置されたシロアリ防除用食毒剤から2メートル離れたところにもシロアリ防除用食毒剤を配置し、シロアリを有効に予防する方法を講じた。
(Example of installation)
The termite control poisoning agent of Example 2 was placed at the corner of the underfloor bottom of the house. In addition, a termite control poisoning agent was placed 2 meters away from the termite control poisoning agent installed in the corner, and a method was taken to effectively prevent termites.
Claims (5)
A method for producing a termite control toxicant, which comprises treating a piece of wood whose surface area is 20% or more of white thick with a chitin synthesis inhibitor.
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JP2001253805A (en) * | 2000-03-10 | 2001-09-18 | Sds Biotech:Kk | Method for controlling termite |
JP2004123669A (en) * | 2002-10-07 | 2004-04-22 | Yuukou Yakuhin Kogyo Kk | Poison bait for exterminating termite |
JP2004217646A (en) * | 2002-12-26 | 2004-08-05 | Ishihara Sangyo Kaisha Ltd | Termite control agent and method for controlling termite |
JP2009107942A (en) * | 2007-10-26 | 2009-05-21 | Xyence Corp | Termite-proofing composition, termite-proofing material and termite-proofing method |
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Publication number | Priority date | Publication date | Assignee | Title |
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JP2001253805A (en) * | 2000-03-10 | 2001-09-18 | Sds Biotech:Kk | Method for controlling termite |
JP2004123669A (en) * | 2002-10-07 | 2004-04-22 | Yuukou Yakuhin Kogyo Kk | Poison bait for exterminating termite |
JP2004217646A (en) * | 2002-12-26 | 2004-08-05 | Ishihara Sangyo Kaisha Ltd | Termite control agent and method for controlling termite |
JP2009107942A (en) * | 2007-10-26 | 2009-05-21 | Xyence Corp | Termite-proofing composition, termite-proofing material and termite-proofing method |
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