JP4966207B2 - 殺虫およびダニ駆除特性を有する活性成分の組み合わせ - Google Patents
殺虫およびダニ駆除特性を有する活性成分の組み合わせ Download PDFInfo
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- JP4966207B2 JP4966207B2 JP2007555515A JP2007555515A JP4966207B2 JP 4966207 B2 JP4966207 B2 JP 4966207B2 JP 2007555515 A JP2007555515 A JP 2007555515A JP 2007555515 A JP2007555515 A JP 2007555515A JP 4966207 B2 JP4966207 B2 JP 4966207B2
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- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 description 1
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- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
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- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical class CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
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- 108700012359 toxins Proteins 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 230000005068 transpiration Effects 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- YDUBPEZBWPRJJL-UHFFFAOYSA-M tributyl-(4-chloro-2-phenylphenoxy)stannane Chemical compound CCCC[Sn](CCCC)(CCCC)OC1=CC=C(Cl)C=C1C1=CC=CC=C1 YDUBPEZBWPRJJL-UHFFFAOYSA-M 0.000 description 1
- HFFZSMFXOBHQLV-UHFFFAOYSA-M tributylstannyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)CCCC HFFZSMFXOBHQLV-UHFFFAOYSA-M 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
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- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
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
- A01N47/02—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 the carbon atom having no bond to a nitrogen atom
- A01N47/04—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 the carbon atom having no bond to a nitrogen atom containing >N—S—C≡(Hal)3 groups
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- 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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- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
Xはハロゲン、アルキル、アルコキシ、ハロアルキル、ハロアルコキシもしくはシアノを表し、
W、YおよびZは、互いに独立して、水素、ハロゲン、アルキル、アルコキシ、ハロアルキル、ハロアルコキシもしくはシアノを表し、
Aは水素、各々の場合において場合によりハロゲン置換されるアルキル、アルコキシアルキル、場合により少なくとも1つの環原子がヘテロ原子で置換される、場合により置換される飽和シクロアルキルを表し、
Bは水素もしくはアルキルを表し、
AおよびBは、これらが結合する炭素原子と共に、飽和もしくは不飽和、非置換もしくは置換される、少なくとも1個のヘテロ原子を場合により含む環を表し、
Dは水素もしくは、アルキル、アルケニル、アルコキシアルキル、場合により1個以上の環構成要素がヘテロ原子で置換される飽和シクロアルキルからなる群からの場合により置換される基を表し、
AおよびDは、これらが結合する原子と共に、非置換であるか、もしくはA、D部分で置換され、および少なくとも1個のヘテロ原子を場合により含む、飽和もしくは不飽和環を表し、
Gは水素(a)を表すか、もしくは以下の基
Eは金属イオンもしくはアンモニウムイオンを表し、
Lは酸素もしくはイオウを表し、
Mは酸素もしくはイオウを表し、
R1は各々の場合において場合によりハロゲン置換されるアルキル、アルケニル、アルコキシアルキル、アルキルチオアルキル、ポリアルコキシアルキルまたは場合によりハロゲン−、アルキル−もしくはアルコキシ−置換される、少なくとも1個のヘテロ原子が割り込んでいてもよい、シクロアルキル、各々の場合において場合により置換されるフェニル、フェニルアルキル、ヘタリール、フェノキシアルキルまたはヘタリールオキシアルキルを表し、
R2は各々の場合において場合によりハロゲン置換されるアルキル、アルケニル、アルコキシアルキル、ポリアルコキシアルキルを表すか、または各々の場合において場合により置換されるシクロアルキル、フェニルもしくはベンジルを表し、
R3は場合によりハロゲン置換されるアルキルもしくは場合により置換されるフェニルを表し、
R4およびR5は、互いに独立して、各々の場合において場合によりハロゲン置換されるアルキル、アルコキシ、アルキルアミノ、ジアルキルアミノ、アルキルチオ、アルケニルチオ、シクロアルキルチオを表すか、または各々の場合において場合により置換されるフェニル、ベンジル、フェノキシもしくはフェニルチオを表し、並びに
R6およびR7は、互いに独立して、水素、各々の場合において場合によりハロゲン置換されるアルキル、シクロアルキル、アルケニル、アルコキシ、アルコキシアルキルを表すか、場合により置換されるフェニルを表すか、場合により置換されるベンジルを表すか、または、これらが結合する窒素原子と共に、場合により置換される、酸素もしくはイオウが場合により割り込む環を表す)
およびDE−A−19653417から公知のエチプロール
Xは、好ましくは、C1−C4−アルキル、C1−C4−アルコキシ、C1−C4−ハロアルキル、フッ素、塩素もしくは臭素を表し、
YおよびZは、互いに独立して、好ましくは、水素、C1−C4−アルキル、ハロゲン、C1−C4−アルコキシもしくはC1−C4−ハロアルキルを表し、
Aは、好ましくは、水素または各々の場合において場合によりハロゲン置換されるC1−C6−アルキルもしくはC3−C8−シクロアルキルを表し、
Bは、好ましくは、水素、メチルもしくはエチルを表し、
A、Bおよびこれらが結合する炭素原子は、好ましくは、場合により1個の環構成要素が酸素もしくはイオウで置換され、およびC1−C4−アルキル、トリフルオロメチルもしくはC1−C4−アルコキシで場合により一もしくは二置換される、飽和C3−C6−シクロアルキルを表し、
Dは、好ましくは、水素、各々の場合において場合によりフッ素−もしくは塩素−置換されるC1−C6−アルキル、C3−C4−アルケニルもしくはC3−C6−シクロアルキルを表し、
AおよびDは、共に、好ましくは、場合により1つのメチレン基がイオウで置換される、場合によりメチル置換されるC3−C4−アルカンジイルを表し、
Gは水素(a)を表すか、もしくは以下の基
Eは金属イオンもしくはアンモニウムイオンを表し、
Lは酸素もしくはイオウを表し、および
Mは酸素もしくはイオウを表し、
R1は、好ましくは、各々の場合において場合によりハロゲン置換されるC1−C10−アルキル、C2−C10−アルケニル、C1−C4−アルコキシ−C1−C4−アルキル、C1−C4−アルキルチオ−C1−C4−アルキルまたは場合によりフッ素−、塩素−、C1−C4−アルキル−もしくはC1−C2−アルコキシ−置換されるC3−C6−シクロアルキルを表し、
場合によりフッ素−、塩素−、臭素−、シアノ−、ニトロ−、C1−C4−アルキル−、C1−C4−アルコキシ−、トリフルオロメチル−もしくはトリフルオロメトキシ−置換されるフェニルを表し、
各々の場合において場合により塩素−もしくはメチル−置換されるピリジルもしくはチエニルを表し、
R2は、好ましくは、各々の場合において場合によりフッ素−もしくは塩素−置換されるC1−C10−アルキル、C2−C10−アルケニル、C1−C4−アルコキシ−C2−C4−アルキルを表し、
場合によりメチル−もしくはメトキシ−置換されるC5−C6−シクロアルキルを表し、または
各々の場合において場合によりフッ素−、塩素−、臭素−、シアノ−、ニトロ−、C1−C4−アルキル−、C1−C4−アルコキシ−、トリフルオロメチル−もしくはトリフルオロメトキシ−置換されるフェニルもしくはベンジルを表し、
R3は、好ましくは、場合によりフッ素置換されるC1−C4−アルキルを表すか、または場合によりフッ素−、塩素−、臭素−、C1−C4−アルキル−、C1−C4−アルコキシ−、トリフルオロメチル−、トリフルオロメトキシ−、シアノ−もしくはニトロ−置換されるフェニルを表し、
R4は、好ましくは、各々の場合において場合によりフッ素−もしくは塩素−置換されるC1−C4−アルキル、C1−C4−アルコキシ、C1−C4−アルキルアミノ、C1−C4−アルキルチオを表すか、または各々の場合において場合によりフッ素−、塩素−、臭素−、ニトロ−、シアノ−、C1−C4−アルコキシ−、トリフルオロメトキシ−、C1−C4−アルキルチオ−、C1−C4−ハロアルキルチオ−、C1−C4−アルキル−もしくはトリフルオロメチル−置換されるフェニル、フェノキシもしくはフェニルチオを表し、
R5は、好ましくは、C1−C4−アルコキシもしくはC1−C4−チオアルキルを表し、
R6は、好ましくは、C1−C6−アルキル、C3−C6−シクロアルキル、C1−C6−アルコキシ、C3−C6−アルケニル、C1−C4−アルコキシ−C1−C4−アルキルを表し、
R7は、好ましくは、C1−C6−アルキル、C3−C6−アルケニルもしくはC1−C4−アルコキシ−C1−C4−アルキルを表し、
R6およびR7は、共に、好ましくは、場合によりメチル−もしくはエチル−置換される、場合により1個の炭素原子が酸素もしくはイオウで置換されるC3−C6−アルキレン基を表す。
Xは、特に好ましくは、塩素、臭素、メチル、エチル、プロピル、i−プロピル、メトキシ、エトキシもしくはトリフルオロメチルを表し、
YおよびZは、互いに独立して、特に好ましくは、水素、フッ素、塩素、臭素、メチル、エチル、プロピル、i−プロピル、トリフルオロメチルもしくはメトキシを表し、
Aは、特に好ましくは、メチル、エチル、プロピル、i−プロピル、ブチル、i−ブチル、sec−ブチル、tert−ブチル、シクロプロピル、シクロペンチルもしくはシクロヘキシルを表し、
Bは、特に好ましくは、水素、メチルもしくはエチルを表し、
A、Bおよびこれらが結合する炭素原子は、特に好ましくは、場合により1個の環構成要素が酸素で置換され、およびメチル、エチル、メトキシ、エトキシ、プロポキシもしくはブトキシで場合により一置換される、飽和C6−シクロアルキルを表し、
Dは、特に好ましくは、水素を表し、メチル、エチル、プロピル、i−プロピル、ブチル、i−ブチル、アリル、シクロプロピル、シクロペンチルもしくはシクロヘキシルを表し、
AおよびDは、共に、特に好ましくは、場合によりメチル置換されるC3−C4−アルカンジイルを表し、
Gは、特に好ましくは、水素(a)を表すか、もしくは以下の基
Mは酸素もしくはイオウを表し、
R1は、特に好ましくは、C1−C8−アルキル、C2−C4−アルケニル、メトキシメチル、エトキシメチル、エチルチオメチル、シクロプロピル、シクロペンチルもしくはシクロヘキシルを表し、
場合によりフッ素−、塩素−、臭素−、シアノ−、ニトロ−、メチル−、エチル−、メトキシ−、トリフルオロメチル−もしくはトリフルオロメトキシ−置換されるフェニルを表し、
各々の場合において場合により塩素−もしくはメチル−置換されるピリジルもしくはチエニルを表し、
R2は、特に好ましくは、C1−C8−アルキル、C2−C4−アルケニル、メトキシエチル、エトキシエチルを表すか、またはフェニルもしくはベンジルを表し、
R6およびR7は、互いに独立して、特に好ましくは、メチル、エチルを表すか、もしくはC3−メチレン基が酸素で置換されるC5−アルキレン基を共に表す。
Xは、特に好ましくは、塩素、臭素もしくはメチルを表し、
YおよびZは、互いに独立して、特に好ましくは、水素、塩素、臭素もしくはメチルを表し、
A、Bおよびこれらが結合する炭素原子は、特に好ましくは、場合により1個の環構成要素が酸素で置換され、およびメチル、メトキシ、エトキシ、プロポキシもしくはブトキシで場合により一置換される、飽和C6−シクロアルキルを表し、
Dは、特に好ましくは、水素を表し、
Gは、特に好ましくは、水素(a)を表すか、もしくは以下の基
Mは酸素もしくはイオウを表し、
R1は、特に好ましくは、C1−C8−アルキル、C2−C4−アルケニル、メトキシメチル、エトキシメチル、エチルメチルチオ、シクロプロピル、シクロペンチル、シクロヘキシルを表し、または
場合によりフッ素−、塩素−、臭素−、メチル−、メトキシ−、トリフルオロメチル−、トリフルオロメトキシ−、シアノ−もしくはニトロ−置換されるフェニルを表し、
各々の場合において場合により塩素−もしくはメチル−置換されるピリジルもしくはチエニルを表し、
R2は、特に好ましくは、C1−C8−アルキル、C2−C4−アルケニル、メトキシエチル、エトキシエチル、フェニルもしくはベンジルを表し、
R6およびR7は、互いに独立して、特に好ましくは、メチル、エチルを表し、もしくはC3−メチレン基が酸素で置換されるC5−アルキレンを共に表す。
特に好ましい混合比:25:1から1:25
これらの混合比は重量比に基づく。この比は式(I)の活性化合物:エチプロールを意味するものと理解されるべきである。
例えば、アンモニウム塩および粉砕天然鉱物、例えば、カオリン、クレー、タルク、チョーク、石英、アタパルガイト、モンモリロナイトもしくは珪藻土、および粉砕合成物質、例えば、高分散シリカ、アルミナおよびケイ酸塩であり;顆粒に適する固体担体は、例えば、破砕および細分化天然岩石、例えば、方解石、大理石、軽石、海泡石および苦灰石、さもなくば、無機および有機粗挽き粉の合成顆粒、並びに有機材料の顆粒、例えば、木屑、ココナッツの殻、トウモロコシ粕およびタバコ茎であり;適切な乳化剤および/もしくは泡形成剤は、例えば、非イオン性およびアニオン性乳化剤、例えば、ポリオキシエチレン脂肪酸エステル、ポリオキシエチレン脂肪アルコールエーテル、例えば、アルキルアリールポリグリコールエーテル、アルキルスルホネート、アルキルスルフェート、アリールスルホネート、さもなくば、タンパク加水分解物であり;適切な分散剤は、例えば、リグノ亜硫酸塩廃液およびメチルセルロースである。
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)、キセストロビウム・ルホビロスム(Xestobium rufovillosum)、プチリヌス・ペクチルニス(Ptilinus pecticornis)、デンドロビウム・ペルチネクス(Dendrobium pertinex)、エルノビウス・モリス(Ernobius mollis)、プリオビウム・カルピニ(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・エクアレ(Trogoxylon aequale)、ミンテス・ルギコリス(Minthes rugicollis)、キシレボルス属種(Xyleborus spp.)、トリプトデンドロン属種(Tryptodendron spp.)、アパテ・モナクス(Apate monachus)、ボストリクス・カプシンス(Bostrychus capucins)、ヘテロボウトリクス・ブルネウス(Heterobostrychus brunneus)、シノキシロン属種(Sinoxylon spp.)、ジノデルス・ミヌツス(Dinoderus minutus)。
シレックス・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)。
カロテルメス・フラビコリス(Kalotermes flavicollis)、クリプトテルメス・ブレビス(Cryptotermes brevis)、ヘテロテルメス・インジコラ(Heterotermes indicola)、レチクリテルメス・フラビペス(Reticulitermes flavipes)、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・ルシフグス(Reticulitermes lucifugus)、マストテルメス・ダルウィニエンシス(Mastotermes darwiniensis)、ズーテルモプシス・ネバデンシス(Zootermopsis nevadensis)、コプトテルメス・ホルモサヌス(Coptotermes formosanus)。
建築用木材、木製の梁、鉄道枕木、橋の構成要素、桟橋、木製の器、箱、パレット、容器、電信柱、木製の羽目板、木製の窓枠およびドア、ベニヤ板、合板、建具類、または家屋建設もしくは建造建具類において極めて一般的に用いられる木製製品。
2−tert−ブチルアミノ−4−シクロプロピルアミノ−6−メチルチオ−1,3,5−トリアジン、ジクロロフェン、ジウロン(diuron)、エンドタール(endothal)、酢酸フェンチン(fentin acetate)、イソプロツロン(isoproturon)、メタベンズチアズロン(methabenzthiazuron)、オキシフルオルフェン(oxyfluorfen)、キノクラミン(quinoclamine)およびテルブトリン(terbutryn);
殺真菌剤、例えば、
ベンゾ[b]チオフェンカルボン酸シクロヘキシルアミドS,S−ジオキシド、ジクロフルアニド、フルオルフォルペット(fluorfolpet)、3−ヨード−2−プロピニルブチルカルバメート、トリルフルアニドおよびアゾール、例えば、
アザコナゾール、シプロコナゾール、エポキシコナゾール、ヘキサコナゾール、メトコナゾール、プロピコナゾールおよびテブコナゾール;
軟体動物駆除剤、例えば、
酢酸フェンチン、メトアルデヒド、メチオカルブ、ニクロサミド(niclosamid)、チオジカルブおよびトリメタカルブ;
もしくは通常の防汚活性化合物、例えば、
4,5−ジクロロ−2−オクチル−4−イソチアゾリン−3−オン、ジヨードメチルパラトリルスルホン、2−(N,N−ジ−メチルチオカルバモイルチオ)−5−ニトロチアジル、2−ピリジンチオール1−オキシドのカリウム、銅、ナトリウムおよび亜鉛塩、ピリジン−トリフェニルボラン、テトラブチルジスタノキサン、2,3,5,6−テトラクロロ−4−(メチルスルホニル)ピリジン、2,4,5,6−テトラクロロイソフタロニトリル、二硫化テトラメチルチウラムおよび2,4,6−トリクロロフェニルマレイミド。
Yが、活性化合物Bをn g/haの適用率もしくはn ppmの濃度で用いるときの、非処理対照のパーセンテージとして表される、殺虫率であり、並びに
Eが、活性化合物AおよびBをmおよびn g/haの適用率もしくはmおよびn ppmの濃度で用いるときの、非処理対照のパーセンテージとして表される、殺虫率である場合、
ミズス・ペルシケ試験
溶媒:7重量部のジメチルホルムアミド
乳化剤:1重量部のアルキルアリールポリグリコールエーテル
活性化合物の適切な調製品を製造するため、1重量部の活性化合物を上記量の溶媒および乳化剤と混合し、この濃縮物を乳化剤含有水で所望の濃度に希釈する。
プルテラ試験
溶媒:7重量部のジメチルホルムアミド
乳化剤:1重量部のアルキルアリールポリグリコールエーテル
活性化合物の適切な調製品を製造するため、1重量部の活性化合物を記載される量の溶媒および乳化剤と混合し、この濃縮物を乳化剤含有水で所望の濃度に希釈する。
臨界濃度試験/土壌昆虫−トランスジェニック植物の処理
試験昆虫:ジアブロチカ・バルテアタ(Diabrotica balteata)−土壌中の幼生
溶媒:7重量部のアセトン
乳化剤:1重量部のアルキルアリールポリグリコールエーテル
活性化合物の適切な調製品を製造するため、1重量部の活性化合物を記載される量の溶媒と混合して記載される量の乳化剤を添加し、この濃縮物を水で所望の濃度に希釈する。
ヘリオチス・ビレセンス試験−トランスジェニック植物の処理
溶媒:7重量部のアセトン
乳化剤:1重量部のアルキルアリールポリグリコールエーテル
活性化合物の適切な調製品を製造するため、1重量部の活性化合物を記載される量の溶媒および記載される量の乳化剤と混合、この濃縮物を水で所望の濃度に希釈する。
Claims (4)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102005008033A DE102005008033A1 (de) | 2005-02-22 | 2005-02-22 | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
DE102005008033.2 | 2005-02-22 | ||
PCT/EP2006/001326 WO2006089665A2 (de) | 2005-02-22 | 2006-02-14 | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
Publications (2)
Publication Number | Publication Date |
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JP2008531488A JP2008531488A (ja) | 2008-08-14 |
JP4966207B2 true JP4966207B2 (ja) | 2012-07-04 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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JP2007555515A Expired - Fee Related JP4966207B2 (ja) | 2005-02-22 | 2006-02-14 | 殺虫およびダニ駆除特性を有する活性成分の組み合わせ |
Country Status (10)
Country | Link |
---|---|
US (1) | US20080287435A1 (ja) |
EP (1) | EP1855532A2 (ja) |
JP (1) | JP4966207B2 (ja) |
KR (1) | KR20070106568A (ja) |
CN (1) | CN101160051B (ja) |
AU (1) | AU2006218277A1 (ja) |
BR (1) | BRPI0607896B1 (ja) |
DE (1) | DE102005008033A1 (ja) |
TW (1) | TW200700009A (ja) |
WO (1) | WO2006089665A2 (ja) |
Cited By (1)
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JP2009542743A (ja) * | 2006-07-11 | 2009-12-03 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | 殺虫及び殺ダニ特性を有する活性成分の組み合わせ |
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DE102004053191A1 (de) * | 2004-11-04 | 2006-05-11 | Bayer Cropscience Ag | 2,6-Diethyl-4-methyl-phenyl substituierte Tetramsäure-Derivate |
DE102005048539A1 (de) * | 2005-10-11 | 2007-04-12 | Bayer Cropscience Ag | Suspensionskonzentrate auf Ölbasis |
DE102006025874A1 (de) | 2006-06-02 | 2007-12-06 | Bayer Cropscience Ag | Alkoxyalkyl-substituierte cyclische Ketoenole |
DE102006027731A1 (de) | 2006-06-16 | 2007-12-20 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
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DE102006033154A1 (de) | 2006-07-18 | 2008-01-24 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
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-
2005
- 2005-02-22 DE DE102005008033A patent/DE102005008033A1/de not_active Withdrawn
-
2006
- 2006-02-14 CN CN2006800125960A patent/CN101160051B/zh not_active Expired - Fee Related
- 2006-02-14 JP JP2007555515A patent/JP4966207B2/ja not_active Expired - Fee Related
- 2006-02-14 WO PCT/EP2006/001326 patent/WO2006089665A2/de active Application Filing
- 2006-02-14 KR KR1020077021285A patent/KR20070106568A/ko not_active Application Discontinuation
- 2006-02-14 US US11/884,845 patent/US20080287435A1/en not_active Abandoned
- 2006-02-14 BR BRPI0607896-6A patent/BRPI0607896B1/pt not_active IP Right Cessation
- 2006-02-14 EP EP06706933A patent/EP1855532A2/de not_active Withdrawn
- 2006-02-14 AU AU2006218277A patent/AU2006218277A1/en not_active Abandoned
- 2006-02-21 TW TW095105681A patent/TW200700009A/zh unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009542743A (ja) * | 2006-07-11 | 2009-12-03 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | 殺虫及び殺ダニ特性を有する活性成分の組み合わせ |
Also Published As
Publication number | Publication date |
---|---|
TW200700009A (en) | 2007-01-01 |
JP2008531488A (ja) | 2008-08-14 |
AU2006218277A1 (en) | 2006-08-31 |
KR20070106568A (ko) | 2007-11-01 |
WO2006089665A3 (de) | 2007-03-01 |
US20080287435A1 (en) | 2008-11-20 |
DE102005008033A1 (de) | 2006-08-24 |
EP1855532A2 (de) | 2007-11-21 |
BRPI0607896B1 (pt) | 2015-06-02 |
CN101160051B (zh) | 2012-12-05 |
WO2006089665A2 (de) | 2006-08-31 |
CN101160051A (zh) | 2008-04-09 |
BRPI0607896A2 (pt) | 2009-10-20 |
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