JP5547075B2 - 昆虫を駆除するための粉剤組成物 - Google Patents
昆虫を駆除するための粉剤組成物 Download PDFInfo
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- JP5547075B2 JP5547075B2 JP2010524360A JP2010524360A JP5547075B2 JP 5547075 B2 JP5547075 B2 JP 5547075B2 JP 2010524360 A JP2010524360 A JP 2010524360A JP 2010524360 A JP2010524360 A JP 2010524360A JP 5547075 B2 JP5547075 B2 JP 5547075B2
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- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
- ZOKXUAHZSKEQSS-UHFFFAOYSA-N tribufos Chemical compound CCCCSP(=O)(SCCCC)SCCCC ZOKXUAHZSKEQSS-UHFFFAOYSA-N 0.000 description 1
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
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Description
(i) GABA拮抗剤から選択される少なくとも1つの殺虫剤および
(ii) セルロースおよびセルロース誘導体から選択される少なくとも1つの有機担体
を含んでなる粉剤組成物、
により達成する。
A.1. 有機(チオ)ホスフェート類:アセフェート、アザメチホス、アジンホス-エチル、アジンホス-メチル、クロルエトキシホス、クロルフェンビンホス、クロルメホス、クロルピリホス、クロルピリホス-メチル、クマホス、シアノホス、デメトン-S-メチル、ダイアジノン、ジクロルボス/DDVP、ジクロトホス、ジメトエート、ジメチルビンホス、ジスルホトン、EPN、エチオン、エトプロホス、ファムフール、フェナミホス、フェニトロチオン、フェンチオン、フルピラゾホス、ホスチアゼート、ヘプテノホス、イソキサチオン、マラチオン、メカルバム、メタミドホス、メチダチオン、メビンホス、モノクロトホス、ナレド、オメトエート、オキシデメトン-メチル、パラチオン、パラチオン-メチル、フェントエート、ホレート、ホサロン、ホスメット、ホスファミドン、ホキシム、ピリミホス-メチル、プロフェノホス、プロペタンホス、プロチオホス、ピラクロホス、ピリダフェンチオン、キナルホス、スルホテップ、テブピリムホス、テメホス、テルブホス、テトラクロルビンホス、チオメトン、トリアゾホス、トリクロルホン、バミドチオン;
A.2. カルバメート類:アルジカルブ、アラニカルブ、ベンジオカルブ、ベンフラカルブ、ブトカルボキシム、ブトキシカルボキシム、カルバリル、カルボフラン、カルボスルファン、エチオフェンカルブ、フェノブカルブ、ホルメタナート、フラチオカルブ、イソプロカルブ、メチオカルブ、メソミル、メトルカルブ、オキサミル、ピリミカルブ、プロポクスル、チオジカルブ、チオファノックス、トリメタカルブ、XMC、キシリルカルブ、トリアザマート;
A.3. ピレスロイド類:アクリナスリン、アレスリン、d-シス-トランス-アレスリン、d-トランス-アレスリン、ビフェントリン、ビオアレスリン、ビオアレスリンS-シクロペンテニル、ビオレスメトリン、シクロプロトリン、シフルトリン、ベータ-シフルトリン、シハロトリン、ラムダ-シハロトリン、ガンマ-シハロトリン、シペルメトリン、アルファ-シペルメトリン、ベータ-シペルメトリン、シータ-シペルメトリン、ゼータ-シペルメトリン、シフェノトリン、デルタメトリン、エンペントリン、エスフェンバレレート、エトフェンプロックス、フェンプロパトリン、フェンバレレート、フルシトリネート、フルメトリン、タウ-フルバリネート、ハロフェンプロックス、イミプロトリン、ペルメトリン、フェノトリン、プラレスリン、レスメトリン、RU 15525、シラフルオフェン、テフルトリン、テトラメトリン、トラロメトリン、トランスフルトリン、ZXI 8901;
A.4. 幼若ホルモン類似物質類:ハイドロプレン、キノプレン、メトプレン、フェノキシカルブ、ピリプロキシフェン;
A.5. ニコチン受容体アゴニスト/アンタゴニスト化合物類:アセタミプリド、ベンスルタップ、カルタップ塩酸塩、クロチアニジン、ジノテフラン、イミダクロプリド、チアメトキサム、ニテンピラム、ニコチン、スピノサド(アロステリックアゴニスト)、チアクロプリド、チオシクラム、チオスルタップ-ナトリウム、およびAKD1022
A.6. クロリドチャネルアクチベーター類:アバメクチン、エマメクチンベンゾエート、ミルベメクチン、レピメクチン;
A.7. METI I化合物類:フェナザキン、フェンピロキシメート、ピリミジフェン、ピリダベン、テブフェンピラド、トルフェンピラド、フルフェネリム、ロテノン;
A.8. METI II及びIII化合物類:アセキノシル、フルアシプリム、ヒドラメチルノン;
A.9. 酸化的リン酸化のアンカップラー類:クロルフェナピル、DNOC;
A.10. 酸化的リン酸化のインヒビター類:アゾシクロチン、シヘキサチン、ジアフェンチウロン、酸化フェンブタスズ、プロパルギット、テトラジホン;
A.11. 脱皮かく乱剤類:シロマジン、クロマフェノジド、ハロフェノジド、メトキシフェノジド、テブフェノジド;
A.12. 協力剤類:ピペロニルブトキシド、トリブホス;
A.13. ナトリウムチャネルブロッカー化合物類:インドキサカルブ、メタフルミゾン;
A.14. 燻蒸剤類:臭化メチル、フッ化クロロピクリンスルフリル;
A.15. 選択的摂食ブロッカー類:クリロタイ、ピメトロジン、フロニカミド;
A.16. ダニ成長インヒビター類:クロフェンテジン、ヘキシチアゾクス、エトキサゾール;
A.17. キチン合成インヒビター類:ブプロフェジン、ビストリフルロン、クロルフルアズロン、ジフルベンズロン、フルシクロクスロン、フルフェノクスロン、ヘキサフルムロン、ルフェヌロン、ノバルロン、ノビフルムロン、テフルベンズロン、トリフルムロン;
A.18. 脂質生合成インヒビター類:スピロジクロフェン、スピロメシフェン、スピロテトラマト;
A.19. オクトパミン作動性アゴニスト類:アミトラズ;
A.20. リアノジン受容体モジュレーター類:フルベンジアミド;
A.21. 各種:リン化アルミニウム、アミドフルメト、ベンクロチアズ、ベンゾキシメート、ビフェナゼート、ほう砂、ブロモプロピレート、シアニド、シエノピラフェン、シフルメトフェン、キノメチオナート、ジコホル、フルオロアセテート、ホスフィン、ピリダリル、ピリフルキナゾン、硫黄、吐酒石;
A.22. N-R’-2,2-ジハロ-1-R’’シクロプロパンカルボキサミド-2-(2,6-ジクロロ-α,α,α-トリフルオロ-p-トリル)ヒドラゾンまたはN-R’-2,2-ジ(R’’’)プロピオンアミド-2-(2,6-ジクロロ-α,α,α-トリフルオロ-p-トリル)-ヒドラゾン(ここで、R’はメチルまたはエチルであり、ハロはクロロまたはブロモであり、R’’は水素またはメチルであり、R’’’はメチルまたはエチルである);
A.23. アントラニルアミド類: クロラントラニリプロール、式Γ2の化合物
A.25. 微生物かく乱剤類:バチルス・チューリンゲンシス亜種イスラエレンシ(Bacillus thuringiensis subsp.Israelensi)、バチルス・スファエリクス(Bacillus sphaericus)、バチルス・チューリンゲンシス亜種アイザワイ(Bacillus thuringiensis subsp.Aizawai)、バチルス・チューリンゲンシス亜種クルスタキ(Bacillus thuringiensis subsp.Kurstaki)、バチルス・チューリンゲンシス亜種テネブリオニス(Bacillus thuringiensis subsp.Tenebrionis)。
(i) 成分(i)、(ii)および(iii)の総重量に基づき0.01〜5、好ましくは0.05〜2、より好ましくは0.1〜1重量%の少なくとも1つの殺虫剤、
(ii) 成分 (i)、(ii)および(iii)の総重量に基づき93〜99.99、好ましくは97〜99.94、より好ましくは98.5〜99.85重量%の少なくとも1つの有機担体、および
(iii) 成分 (i)、(ii)および(iii)の総重量に基づき、0〜2 %、好ましくは0.01〜1、より好ましくは0.05〜0.5重量%の、少なくとも1つの蛍光色素
を含んでなる。
(i) 粉剤組成物の総重量に基づき、0.01〜5、好ましくは0.05〜2、より好ましくは0.1〜1重量%の少なくとも1つの殺虫剤、
(ii) 粉剤組成物の総重量に基づき、93〜99.99、好ましくは97〜99.94、より好ましくは98.5〜99.85重量%の少なくとも1つの有機担体、および
(iii) 粉剤組成物の総重量に基づき、0〜2%、好ましくは0.01〜1、より好ましくは0.05〜0.5重量%の少なくとも1つの蛍光色素
を含む。
鞘翅目、例えば
ヒロトルペス・バジュルス(Hylotrupes bajulus)、クロロホルス・ピロシス(Chlorophorus pilosis)、アノビウム・プンクタツム(Anobium punctatum)、キセストビウム・ルフォビロスム(Xestobium rufovillosum)、プチリヌス・ペクチコルニス(Ptilinus pecticornis)、デンドロビウム・ペルチネキス(Dendrobium pertinex)、エルノビウス・モリス(Ernobius mollis)、プリオビウム・カロピニ(Priobium carpini)、リクツス・ブルネウス(Lyctus brunneus)、リクツス・アフリカヌス(Lyctus africanus)、リクツス・プラニコリス(Lyctus planicollis)、リクツス・リネアリス(Lyctus linearis)、リクツス・プベセンス(Lyctus pubescens)、トロゴキシロン・アエクアレ(Trogoxylon aequale)、ミンテス・ルギコリス(Minthes rugicollis)、キシレボルス種(Xyleborus spec.)、トリポトデンドロン種(Tryptodendron spec.)、アパテ・モナクス(Apate monachus)、ボストリクス・カプシンス(Bostrychus capucins)、ヘテロボストリクス・ブルネウス(Heterobostrychus brunneus)、シノキシロン 種(Sinoxylon spec.)、ジノデルス・ミヌツス(Dinoderus minutus);
膜翅目、例えば
シレクス・ジュベンクス(Sirex juvencus)、ウロセルス・ギガス(Urocerus gigas)、ウロセルス・ギガス・タイグヌス(Urocerus gigas taignus)、ウロセルス・アウグル(Urocerus augur);
シロアリ(等翅目類)、例えばカロテルメス種(Calotermes spp)、例えばカロテルメス・フラビコリス(Calotermes flavicollis)、コプトテルメス種(Coptotermes spp.)、例えばコプトテルメス・アシナシフォルミス(Coptotermes acinaciformis)、コプトテルメス・フォルモサヌス(Coptotermes formosanus)、コプトテルメス・ハビランディ(Coptotermes havilandi)もしくはコプトテルメス・ラクテウス(Coptotermes lacteus)、クリプトテルメス種(Cryptotermes spp.)、例えばクリプトテルメス・ブレビス(Cryptotermes brevis)、ヘテロテルメス種(Heterotermes spp.)、例えばヘテロテルメス・オーレウス(Heterotermes aureus)もしくはヘテロテルメス・インジコラ(Heterotermes indicola)、ロイコテルメス種(Leucotermes spp.)、例えばロイコテルメス・フラビペス(Leucotermes flavipes)、マストテルメス種(Mastotermes spp.)、例えばマストテルメス・ダルウィニエンシス(Mastotermes darwiniensis)、レチクリテルメス種(Reticulitermes spp.)、例えばレチクリテルメス・アレニコラ(Reticulitermes arenicola)、レチクリテルメス・フラビペス(Reticulitermes flavipes)、レチクリテルメス・ハジェニ(Reticulitermes hageni)、レチクリテルメス・ハジェヌス(Reticulitermes hagenus)、レチクリテルメス・ヘスペルス(Reticulitermes hesperus)、レチクリテルメス・ルシフグス(Reticulitermes lucifugus)、レチクリテルメス・サントネンシス(Reticulitermes santonensis)、レチクリテルメス・セパラタス(Reticulitermes speratus)、レチクリテルメス・ティビアリス(Reticulitermes tibialis)もしくはレチクリテルメス・バージニカス(Reticulitermes virginicus)、シェドリノテルメス種(Schedorhinotermes spp.)、例えばシェドリノテルメス・インテルメディウス(Schedorhinotermes intermedius)、テルメス種(Termes spp.)、例えばテルメス・ナタレンシス(Termes natalensis)、ズーテルモプシス種(Zootermopsis spp.)、例えばズーテルモプシス・ネバデンシス(Zootermopsis nevadensis);
シミ目、例えば、レピスマ・サッカリナ(Lepisma saccharina)。
1.1
0.5重量%のフィプロニル、0.1重量%の蛍光ピグメントLumogen Yellow SO 790 (BASF AG)および99.4重量%のα-セルロースを含有するDP(分散性粉末)として製剤化された粉剤組成物を以下のように調製した。すなわち、15.6 gのフィプロニル(市販の製品Termidor 80WGの形態で使用)、2.5 gのLumogen色素および約100gのα-セルロースを、KnifeTechミル装置(密閉容器)内で粉砕および混合することにより、各バッチについて別々のコンテナの予備混合物を調製した。2.4 gのα-セルロースを20 L HDPEコンテナ内に入れ、予備調製バッチロードの予備混合物の内容物を投入した。次いで混合物をドラム混合機に入れ、1時間混合した。
実施例1.1と同様に、0.5重量%のフィプロニルおよび95.5重量%のセルロースアセテートを含有する粉剤組成物を調製した。
2.1 実験室実験
この実施例では実施例1.2の組成物を用いた。比較例として、0.6重量%のタルカム粉末上三酸化ヒ素を含有する粉剤組成物を使用した。
いずれの粉末製剤も、ロール法または吹送法のいずれを用いた場合にも、両方の種に対して100%の致死性をもたらした。すなわち、コプトテルメス・アシナシフォルミス(C. acinaciformis)は8〜9時間曝露後、およびマストテルメス・ダルウィニエンシス(M. darwiniensis)は21〜23時間曝露後に、死に至った。三酸化ヒ素は本発明の配合物と比較して、100%致死性を達成するのが早かった。したがって本発明の配合物を用いた処置は、毒物がさらに移送されてコロニー全体に行き渡るための時間をより多く提供する。
実施例1.1の粉末製剤の餌箱増殖マストテルメス・ダルウィニエンシス(Mastotermes darwiniensis)に対する根治的処置としての効力を、Forrest Beach, north Queensland, Australiaにおける家庭内環境において評価した。未処置の加工材木で満たされた餌箱内で増殖させたシロアリの巨大な個体群を手持ち型の吹送器によりフィプロニル粉剤で局所処置した。攻撃されている近接したヤシの木をモニタリング点としてそのままにした。処置から12日後に、マストテルメス・ダルウィニエンシス(Mastotermes darwiniensis)蔓延は撲滅された。
実施例1.1の粉末製剤のマストテルメス・ダルウィニエンシス(Mastotermes darwiniensis)に対する根治的処置としての効力を、Townsville, north Queensland, Australiaにおける家庭内環境において評価した。古い木材製の荷馬車内にシロアリ蔓延が存在した。実施例1.1の粉末製剤を、標準的な手持ち型吹送器を用いて可能な限り多くのシロアリに局所適用した。これは荷馬車の車輪にのみ行われ、他の部位はモニタリングのためにそのままにした。処置の19日後には、マストテルメス・ダルウィニエンシス(Mastotermes darwiniensis)蔓延は撲滅された。
コプトテルメス種(Coptotermes sp)に対する根治的処置としての実施例1.1の粉末製剤の効力を、Macksville, New South Wales, Australiaにおける家庭内環境において評価した。活動的なシロアリ蔓延がある家屋の浴室に存在した。実施例1.1の粉末製剤を、標準的な手持ち型吹送器を用いて可能な限り多くのシロアリに局所適用した。処置の13日後に、コプトテルメス蔓延は撲滅された。
コプトテルメス・アシナシフォルミス(Coptotermes acinaciformis)に対する根治的処置としての実施例1.1の粉末製剤の効力をBrunswick Heads, New South Wales, Australiaにおける家庭内環境において評価した。活動的なシロアリ蔓延は家屋全体にわたり存在した。実施例1.1の粉末製剤を、標準的な手持ち型吹送器を用いて可能な限り多くのシロアリに局所適用した。処置の16日後に、甚大であったコプトテルメス・アシナシフォルミス(Coptotermes acinaciformis)蔓延は撲滅された。
害虫駆除専門家は、局所処置後の残された実施例1.1の粉末製剤がシロアリにより摂食されたことを報告した。
Claims (19)
- (i) GABA拮抗剤から選択される少なくとも1つの殺虫剤および
(ii) α-セルロース
を含んでなる粉剤組成物。 - GABA拮抗剤が式IIのフェニルピラゾール化合物から選択される、請求項2記載の粉剤組成物。
- Raがエチルまたはトリフルオロメチルである、請求項2または3記載の粉剤組成物。
- GABA拮抗剤がフィプロニルである請求項2〜4のいずれか1項記載の粉剤組成物。
- (iii) 少なくとも1つの蛍光色素
をさらに含んでなる請求項1〜5のいずれか1項記載の粉剤組成物。 - (i) 粉剤組成物の総重量に基づき、0.01〜5重量%の少なくとも1つの殺虫剤、
(ii) 粉剤組成物の総重量に基づき、93〜99.99重量%のα-セルロース、および
(iii) 粉剤組成物の総重量に基づき、0〜2重量%の少なくとも1つの蛍光色素
を含む、
請求項1〜6のいずれか1項記載の粉剤組成物。 - (i) GABA拮抗剤から選択される少なくとも1つの殺虫剤
(ii) セルロースおよびセルロース誘導体から選択される少なくとも1つの有機担体、および
(iii) ナフタレン類(特にナフチルイミド類)、ペリレン類(ペリレン類およびペリレンイミド類)、テリレン類(テリレン類およびテリレンイミド類)、クアテリレン類(クアテリレン類およびクアテリレンイミド類)、クマリン類、キサンテン類、チオキサンテン類、ナフトラクタム類、アザラクトン類、メチン類、チアジン類、ならびにチオインジゴイドから選択される少なくとも1つの蛍光色素、
を含む粉剤組成物。 - 前記少なくとも1つの有機担体が昆虫に食べられ得るものである、請求項8記載の粉剤組成物。
- セルロースがα-セルロースである、請求項8または9記載の粉剤組成物。
- セルロース誘導体がセルロースアセテートである、請求項8または9記載の粉剤組成物。
- 蛍光色素がルモジェン・イエロー(Lumogen Yellow)SO 790である、請求項8〜11のいずれか1項記載の粉剤組成物。
- (i) 粉剤組成物の総重量に基づき、0.05〜2重量%の少なくとも1つの殺虫剤、
(ii) 粉剤組成物の総重量に基づき、97〜99.94重量%の少なくとも1つの有機担体、および
(iii) 粉剤組成物の総重量に基づき、0.01〜1重量%の少なくとも1つの蛍光色素
を含んでなる、請求項8〜12のいずれか1項記載の粉剤組成物。 - 粒径400μm未満の、請求項1〜13のいずれか1項記載の粉剤組成物。
- 昆虫を駆除するための、請求項1〜14のいずれか1項記載の粉剤組成物の使用。
- シロアリを駆除するための、請求項15記載の使用。
- 昆虫を防除する方法であって、昆虫、その食糧源もしくはその生息環境、または昆虫の攻撃もしくは蔓延から保護すべき材料、土壌、表面もしくは空間を殺虫的に有効な量の請求項1〜14のいずれか1項記載の粉剤組成物と接触させることを含む前記方法。
- シロアリを防除するための、請求項17記載の方法。
- 木材をシロアリの攻撃もしくは蔓延から保護する方法であって、保護すべき材料、または保護すべき木材の側にある土壌、表面もしくは空間を殺虫的に有効な量の請求項1〜14のいずれか1項記載の粉剤組成物と接触させることを含む前記方法。
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PCT/EP2007/059833 WO2009036797A1 (en) | 2007-09-18 | 2007-09-18 | Dust composition for combating insects |
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JP2010539109A5 JP2010539109A5 (ja) | 2013-02-14 |
JP5547075B2 true JP5547075B2 (ja) | 2014-07-09 |
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US (1) | US20100203098A1 (ja) |
EP (1) | EP2194789A1 (ja) |
JP (1) | JP5547075B2 (ja) |
KR (1) | KR20100059984A (ja) |
CN (1) | CN101827526A (ja) |
AU (1) | AU2007359137B2 (ja) |
BR (1) | BRPI0721963A2 (ja) |
EA (1) | EA017881B1 (ja) |
EG (1) | EG25948A (ja) |
MX (1) | MX2010002946A (ja) |
WO (1) | WO2009036797A1 (ja) |
ZA (1) | ZA201002633B (ja) |
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JP5683569B2 (ja) | 2009-04-28 | 2015-03-11 | ビーエーエスエフ コーポレーション | 発泡性駆除薬組成物 |
JP5675776B2 (ja) * | 2009-04-28 | 2015-02-25 | ビーエーエスエフ コーポレーション | 殺有害生物剤組成物及び散布機 |
CN102595881A (zh) | 2009-08-28 | 2012-07-18 | 巴斯夫公司 | 可发泡农药组合物及施用方法 |
JP6170673B2 (ja) | 2012-12-27 | 2017-07-26 | 富士フイルム株式会社 | カラーフィルタ用組成物、赤外線透過フィルタ及びその製造方法、並びに赤外線センサー |
CN106106477B (zh) * | 2016-06-27 | 2018-09-21 | 青岛润生农化有限公司 | 含甲维盐与乙酰虫腈的杀虫组合物 |
KR102524157B1 (ko) * | 2022-09-19 | 2023-04-20 | 한국전통문화대학교산학협력단 | 국내서식흰개미 제어용 분말형 약제 및 이의 제조방법 |
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US5151443A (en) * | 1990-07-20 | 1992-09-29 | Sandoz Ltd. | Method of controlling termites |
IL105772A (en) * | 1992-06-01 | 1998-07-15 | Univ Florida | Methods and materials for pest control |
WO1998021960A1 (fr) * | 1996-11-22 | 1998-05-28 | Rhone-Poulenc Agrochimie | Nouvelles compositions solides a base de derive cellulosique insoluble et de derive de 1-aryl-pyrazole |
DE19734665A1 (de) * | 1997-08-11 | 1999-02-18 | Bayer Ag | Mittel gegen holzzerstörende Insekten |
JP2002020201A (ja) * | 2000-06-30 | 2002-01-23 | Fumakilla Ltd | 匍匐害虫及び/又は害獣駆除用毒餌剤並びに該毒餌剤を用いた匍匐害虫及び/又は害獣駆除方法 |
WO2002015684A1 (en) * | 2000-08-23 | 2002-02-28 | Bayer Cropscience S.A. | Impregnated wood compositions useful for termite control |
US6416752B1 (en) * | 2001-01-04 | 2002-07-09 | Whitmire Micro-Gen Research Laboratories, Inc. | Termite bait composition and method |
JP4324391B2 (ja) * | 2002-02-22 | 2009-09-02 | 石原産業株式会社 | 家屋害虫防除用組成物及び家屋害虫の防除方法 |
JP4222470B2 (ja) * | 2002-09-19 | 2009-02-12 | 住化エンビロサイエンス株式会社 | シロアリ用防除組成物および当該組成物を用いたシロアリ防除方法 |
JP2004217646A (ja) * | 2002-12-26 | 2004-08-05 | Ishihara Sangyo Kaisha Ltd | シロアリ防除剤及びシロアリの防除方法 |
SI1599463T1 (sl) * | 2003-01-28 | 2013-10-30 | E.I. Du Pont De Nemours And Company | Ciano antranilamidni insekticidi |
AU2005228402B2 (en) * | 2004-03-29 | 2011-03-31 | Dow Agrosciences Llc | Pesticide compositions |
BRPI0509413A (pt) * | 2004-04-13 | 2007-09-04 | Du Pont | composto, composição de controle de pragas invertebradas, métodos de controle de pragas invertebradas, composições de pulverização e de isca e dispositivo de controle de pragas invertebradas |
SG155230A1 (en) * | 2004-08-25 | 2009-09-30 | Bayer Cropscience Lp | Method of controlling termites |
WO2006083948A2 (en) * | 2005-02-02 | 2006-08-10 | Fmc Corporation | Fine particles as a delivery system for termite toxicants |
CN101123997A (zh) * | 2005-02-03 | 2008-02-13 | Fmc有限公司 | 使用毒饵中的液态杀白蚁剂防治白蚁的方法 |
CN103461303B (zh) * | 2006-12-21 | 2018-05-08 | 美国陶氏益农公司 | 包括热塑性聚合物、害虫食物材料和杀虫剂的复合材料 |
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- 2007-09-18 AU AU2007359137A patent/AU2007359137B2/en active Active
- 2007-09-18 US US12/678,413 patent/US20100203098A1/en not_active Abandoned
- 2007-09-18 EP EP07820296A patent/EP2194789A1/en not_active Withdrawn
- 2007-09-18 WO PCT/EP2007/059833 patent/WO2009036797A1/en active Application Filing
- 2007-09-18 MX MX2010002946A patent/MX2010002946A/es unknown
- 2007-09-18 BR BRPI0721963-6A patent/BRPI0721963A2/pt not_active IP Right Cessation
- 2007-09-18 KR KR1020107008299A patent/KR20100059984A/ko not_active Application Discontinuation
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- 2007-09-18 CN CN200780101139A patent/CN101827526A/zh active Pending
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US20100203098A1 (en) | 2010-08-12 |
EP2194789A1 (en) | 2010-06-16 |
CN101827526A (zh) | 2010-09-08 |
EA201000435A1 (ru) | 2010-10-29 |
AU2007359137A1 (en) | 2009-03-26 |
JP2010539109A (ja) | 2010-12-16 |
WO2009036797A1 (en) | 2009-03-26 |
AU2007359137B2 (en) | 2014-03-20 |
MX2010002946A (es) | 2010-03-31 |
KR20100059984A (ko) | 2010-06-04 |
EA017881B1 (ru) | 2013-03-29 |
EG25948A (en) | 2012-11-11 |
BRPI0721963A2 (pt) | 2014-05-20 |
ZA201002633B (en) | 2015-08-26 |
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