JP2009507799A - 農薬の効果を改善するための乳酸エステルの使用 - Google Patents
農薬の効果を改善するための乳酸エステルの使用 Download PDFInfo
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- JP2009507799A JP2009507799A JP2008529514A JP2008529514A JP2009507799A JP 2009507799 A JP2009507799 A JP 2009507799A JP 2008529514 A JP2008529514 A JP 2008529514A JP 2008529514 A JP2008529514 A JP 2008529514A JP 2009507799 A JP2009507799 A JP 2009507799A
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- Prior art keywords
- methyl
- crop protection
- esters
- lactic acid
- formula
- Prior art date
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- QYPNKSZPJQQLRK-UHFFFAOYSA-N tebufenozide Chemical compound C1=CC(CC)=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 QYPNKSZPJQQLRK-UHFFFAOYSA-N 0.000 description 1
- ZZYSLNWGKKDOML-UHFFFAOYSA-N tebufenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(=CC=2)C(C)(C)C)=C1Cl ZZYSLNWGKKDOML-UHFFFAOYSA-N 0.000 description 1
- 239000004558 technical concentrate Substances 0.000 description 1
- 239000004557 technical material Substances 0.000 description 1
- CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 description 1
- WWJZWCUNLNYYAU-UHFFFAOYSA-N temephos Chemical compound C1=CC(OP(=S)(OC)OC)=CC=C1SC1=CC=C(OP(=S)(OC)OC)C=C1 WWJZWCUNLNYYAU-UHFFFAOYSA-N 0.000 description 1
- DOMXUEMWDBAQBQ-WEVVVXLNSA-N terbinafine Chemical compound C1=CC=C2C(CN(C\C=C\C#CC(C)(C)C)C)=CC=CC2=C1 DOMXUEMWDBAQBQ-WEVVVXLNSA-N 0.000 description 1
- 229960002722 terbinafine Drugs 0.000 description 1
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
- IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 1
- 229960005199 tetramethrin Drugs 0.000 description 1
- 239000004308 thiabendazole Substances 0.000 description 1
- 235000010296 thiabendazole Nutrition 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 description 1
- 125000004305 thiazinyl group Chemical group S1NC(=CC=C1)* 0.000 description 1
- AHTPATJNIAFOLR-UHFFFAOYSA-N thifensulfuron-methyl Chemical group S1C=CC(S(=O)(=O)NC(=O)NC=2N=C(OC)N=C(C)N=2)=C1C(=O)OC AHTPATJNIAFOLR-UHFFFAOYSA-N 0.000 description 1
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
- OPASCBHCTNRLRM-UHFFFAOYSA-N thiometon Chemical compound CCSCCSP(=S)(OC)OC OPASCBHCTNRLRM-UHFFFAOYSA-N 0.000 description 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- QSOHVSNIQHGFJU-UHFFFAOYSA-L thiosultap disodium Chemical compound [Na+].[Na+].[O-]S(=O)(=O)SCC(N(C)C)CSS([O-])(=O)=O QSOHVSNIQHGFJU-UHFFFAOYSA-L 0.000 description 1
- 229960002447 thiram Drugs 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
- 229940074152 thuringiensin Drugs 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- WPALTCMYPARVNV-UHFFFAOYSA-N tolfenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(OC=3C=CC(C)=CC=3)=CC=2)=C1Cl WPALTCMYPARVNV-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
- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 description 1
- DDVNRFNDOPPVQJ-HQJQHLMTSA-N transfluthrin Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=C(F)C(F)=CC(F)=C1F DDVNRFNDOPPVQJ-HQJQHLMTSA-N 0.000 description 1
- 230000009261 transgenic effect Effects 0.000 description 1
- 230000014616 translation Effects 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 description 1
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 description 1
- YMXOXAPKZDWXLY-QWRGUYRKSA-N tribenuron methyl Chemical group COC(=O)[C@H]1CCCC[C@@H]1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 YMXOXAPKZDWXLY-QWRGUYRKSA-N 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-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
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000004555 ultra-low volume (ULV) suspension Substances 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 description 1
- DBXFMOWZRXXBRN-LWKPJOBUSA-N valifenalate Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)NC(CC(=O)OC)C1=CC=C(Cl)C=C1 DBXFMOWZRXXBRN-LWKPJOBUSA-N 0.000 description 1
- LESVOLZBIFDZGS-UHFFFAOYSA-N vamidothion Chemical compound CNC(=O)C(C)SCCSP(=O)(OC)OC LESVOLZBIFDZGS-UHFFFAOYSA-N 0.000 description 1
- 239000004561 vapour releasing product Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- BCEHBSKCWLPMDN-MGPLVRAMSA-N voriconazole Chemical compound C1([C@H](C)[C@](O)(CN2N=CN=C2)C=2C(=CC(F)=CC=2)F)=NC=NC=C1F BCEHBSKCWLPMDN-MGPLVRAMSA-N 0.000 description 1
- 229960004740 voriconazole Drugs 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000004565 water dispersible tablet Substances 0.000 description 1
- 239000004520 water soluble gel Substances 0.000 description 1
- 239000004549 water soluble granule Substances 0.000 description 1
- 239000004552 water soluble powder Substances 0.000 description 1
- 239000004553 water soluble powder for seed treatment Substances 0.000 description 1
- 239000004554 water soluble tablet Substances 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- WCJYTPVNMWIZCG-UHFFFAOYSA-N xylylcarb Chemical compound CNC(=O)OC1=CC=C(C)C(C)=C1 WCJYTPVNMWIZCG-UHFFFAOYSA-N 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 description 1
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/30—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
・ 0.01〜3%(重量/容積)であり、
・ 特に好ましくは、0.01〜1%(重量/容積)であり、
・ 極めて特に好ましくは、0.02〜0.5%(重量/容積)であり、
・ とりわけ好ましくは、0.03〜0.3%(重量/容積)である。
核酸合成の阻害薬
ベナラキシル、ベナラキシル−M、ブピリメート、キララキシル(chiralaxyl)、クロジラコン、ジメチリモール、エチリモール、フララキシル、ヒメキサゾール、メフェノキサム、メタラキシル、メタラキシル−M、オフラセ、オキサジキシル、オキソリン酸;
有糸分裂及び細胞分裂の阻害薬
ベノミル、カルベンダジム、ジエトフェンカルブ、エタボキサム、フベリダゾール、ペンシクロン、チアベンダゾール、チオファネート−メチル、ゾキサミド;
呼吸鎖複合体Iの阻害薬
ジフルメトリム;
呼吸鎖複合体IIの阻害薬
ボスカリド、カルボキシン、フェンフラム、フルトラニル、フラメトピル、フルメシクロックス、メプロニル、オキシカルボキシン、ペンチオピラド、チフルザミド;
呼吸鎖複合体IIIの阻害薬
アゾキシストロビン、シアゾファミド、ジモキシストロビン、エネストロビン(enestrobin)、ファモキサドン、フェンアミドン、フルオキサストロビン、クレソキシム−メチル、メトミノストロビン、オリサストロビン、ピラクロストロビン、ピコキシストロビン、トリフロキシストロビン;
デカップラー
ジノカップ、フルアジナム;
ATP産生の阻害薬
酢酸トリフェニルスズ、塩化トリフェニルスズ、水酸化トリフェニルスズ、シルチオファム;
アミノ酸生合成及びタンパク質生合成の阻害薬
アンドプリム(andoprim)、ブラストサイジン−S、シプロジニル、カスガマイシン、カスガマイシン塩酸塩水和物、メパニピリム、ピリメタニル;
シグナル伝達の阻害薬
フェンピクロニル、フルジオキソニル、キノキシフェン;
脂質及び膜合成の阻害薬
クロゾリネート、イプロジオン、プロシミドン、ビンクロゾリン、
アンプロピルホス、カリウム−アンプロピルホス、エジフェンホス、エトリジアゾール、イプロベンホス(IBP)、イソプロチオラン、ピラゾホス、
トルクロホス−メチル、ビフェニル、
ヨードカルブ(iodocarb)、プロパモカルブ、プロパモカルブ塩酸塩、プロパモカルブホセチレート(propamocarbfosetylate);
エルゴステロール生合成の阻害薬
フェンヘキサミド、
アザコナゾール、ビテルタノール、ブロムコナゾール、シプロコナゾール、ジクロブトラゾール、ジフェノコナゾール、ジニコナゾール、ジニコナゾール−M、エポキシコナゾール、エタコナゾール、フェナリモール、フェンブコナゾール、フルキンコナゾール、フルルプリミドール、フルシラゾール、フルトリアホール、フルコナゾール、フルコナゾール−シス、ヘキサコナゾール、イマザリル、硫酸イマザリル、イミベンコナゾール、イプコナゾール、メトコナゾール、ミクロブタニル、ヌアリモール、オキシポコナゾール、パクロブトラゾール、ペンコナゾール、ペフラゾエート、プロクロラズ、プロピコナゾール、プロチオコナゾール、ピリフェノックス、シメコナゾール、テブコナゾール、テトラコナゾール、トリアジメホン、トリアジメノール、トリフルミゾール、トリホリン(triforing)、トリチコナゾール、ウニコナゾール、ボリコナゾール、ビニコナゾール、
アルジモルフ、ドデモルフ、酢酸ドデモルフ、フェンプロピジン、フェンプロピモルフ、スピロキサミン、トリデモルフ、ナフチフィン、ピリブチカルブ、テルビナフィン;
細胞壁合成の阻害薬
ベンチアバリカルブ、ビアラホス、ジメトモルフ、フルモルフ(flumorph)、イプロバリカルブ、マンジプロパミド、ポリオキシン、ポリオキソリム、バリダマイシンA;
メラニン生合成の阻害薬
カルプロパミド、ジクロシメット、フェノキサニル、フタリド、ピロキロン、トリシクラゾール;
抵抗性誘導薬
アシベンゾラル−S−メチル、プロベナゾール、チアジニル;
多部位
カプタホール、キャプタン、クロロタロニル、銅塩、例えば、水酸化銅、ナフテン酸銅、塩基性塩化銅、硫酸銅、酸化銅、オキシン銅及びボルドー液、ジクロフルアニド、ジチアノン、ドジン、ドジン遊離塩基、ファーバム、ホルペット、フルオロホルペット、グアザチン、酢酸グアザチン、イミノクタジン、イミノクタジンアルベシル酸塩、イミノクタジン三酢酸塩、マンカッパー、マンゼブ、マンネブ、メチラム、メチラム亜鉛(metiram zinc)、プロピネブ、硫黄及び多硫化カルシウム含有硫黄剤、チウラム、トリルフルアニド、ジネブ、ジラム;
さらなる殺菌剤
アミブロムドール(amibromdol)、ベンチアゾール、ベトキサジン(bethoxazin)、カプシマイシン(capsimycin)、カルボン、キノメチオネート、クロロピクリン、クフラネブ、シフルフェナミド、シモキサニル、ダゾメット、デバカルブ(debacarb)、ジクロメジン、ジクロロフェン、ジクロラン、ジフェンゾコート、ジフェンゾコートメチル硫酸塩、ジフェニルアミン、フェリムゾン、フルメトベル、フルスルファミド、フルオピコリド、フルオルイミド、ホセチル−アルミニウム、ホセチル−カルシウム、ホセチル−ナトリウム、ヘキサクロロベンゼン、8−ヒドロキシキノリン硫酸、イルママイシン、メタスルホカルブ、メトラフェノン、メチルイソチオシアネート、ミルディオマイシン、ナタマイシン、ジメチルジチオカルバミン酸ニッケル、ニトロタル−イソプロピル、オクチリノン、オキサモカルブ(oxamocarb)、オキシフェンチイン(oxyfenthiin)、ペンタクロロフェノール及び塩、2−フェニルフェノール及び塩、ピペラリン(piperalin)、プロパノシン−ナトリウム(propanosine-sodium)、プロキナジド、ピリベンカルブ、ピロールニトリン、キントゼン、テクロフタラム、テクナゼン、トリアゾキシド、トリクラミド、バリフェナール(valiphenal)、ザリラミド、
2−(2−{[6−(3−クロロ−2−メチルフェノキシ)−5−フルオロピリミジン−4−イル)オキシ}フェニル)−2−(メトキシイミノ)−N−メチルアセトアミド、
2−[[[[1−[3−(1−フルオロ−2−フェニルエチル)オキシ]フェニル]エチリデン]アミノ]オキシ]メチル]−α−(メトキシイミノ)−N−メチル−α−ベンズアセトアミド、
シス−1−(4−クロロフェニル)−2−(1H−1,2,4−トリアゾール−1−イル)シクロヘプタノール、
1−[(4−メトキシフェノキシ)メチル]−2,2−ジメチルプロピル−1H−イミダゾール−1−カルボン酸、
2,3,5,6−テトラクロロ−4−(メチルスルホニル)ピリジン、
2−ブトキシ−6−ヨード−3−プロピルベンゾピラノン−4−オン、
2−クロロ−N−(2,3−ジヒドロ−1,1,3−トリメチル−1H−インデン−4−イル)−3−ピリジンカルボキサミド、
3,4,5−トリクロロ−2,6−ピリジンジカルボニトリル、
3,4−ジクロロ−N−(2−シアノフェニル)イソチアゾール−5−カルボキサミド(イソチアニル(isotianil))、
3−[5−(4−クロロフェニル)−2,3−ジメチルイソオキサゾリジン−3−イル]ピリジン、
5−クロロ−6−(2,4,6−トリフルオロフェニル)−N−[(1R)−1,2,2−トリメチルプロピル][1,2,4]トリアゾロ[1,5−a]ピリミジン−7−アミン、
5−クロロ−7−(4−メチルピペリジン−1−イル)−6−(2,4,6−トリフルオロフェニル)[1,2,4]トリアゾロ[1,5−a]ピリミジン、
5−クロロ−N−[(1R)−1,2−ジメチルプロピル]−6−(2,4,6−トリフルオロフェニル)[1,2,4]トリアゾロ[1,5−a]ピリミジン−7−アミン、
2−[[[シクロプロピル−[(4−メトキシフェニル)イミノ]メチル]チオ]メチル]−α−(メトキシメチレン)ベンズ酢酸メチル、
1−(2,3−ジヒドロ−2,2−ジメチル−1H−インデン−1−イル)−1H−イミダゾール−5−カルボン酸メチル、
N−(3’,4’−ジクロロ−5−フルオロビフェニル−2−イル)−3−(ジフルオロメチル)−1−メチル−lH−ピラゾール−4−カルボキサミド、
N−(3−エチル−3,5,5−トリメチルシクロヘキシル)−3−ホルミルアミノ−2−ヒドロキシベンズアミド、
N−(4−クロロ−2−ニトロフェニル)−N−エチル−4−メチルベンゼンスルホンアミド、
N−(4−クロロベンジル)−3−[3−メトキシ−4−(プロプ−2−イン−1−イルオキシ)フェニル]プロパンアミド、
N−[(4−クロロフェニル)(シアノ)メチル]−3−[3−メトキシ−4−(プロプ−2−イン−1−イルオキシ)フェニル]プロパンアミド、
N−(5−ブロモ−3−クロロピリジン−2−イル)メチル−2,4−ジクロロニコチンアミド、
N−[1−(5−ブロモ−3−クロロピリジン−2−イル)エチル]−2,4−ジクロロニコチンアミド、
(2S)−N−[2−[4−[[3−(4−クロロフェニル)−2−プロピニル]オキシ]−3−メトキシフェニル]エチル]−3−メチル−2−[(メチルスルホニル)アミノ]ブタンアミド、
N−{(Z)−[(シクロプロピルメトキシ)イミノ][6−(ジフルオロメトキシ)−2,3−ジフルオロフェニル]メチル}−2−ベンズアセトアミド、
N−{2−[1,1’−ビ(シクロプロピル)−2−イル]フェニル}−3−(ジフルオロメチル)−1−メチル−1H−ピラゾール−4−カルボキサミド、
N−{2−[3−クロロ−5−(トリフルオロメチル)ピリジン−2−イル]エチル}−2−(トリフルオロメチル)ベンズアミド、
N−エチル−N−メチル−N’−{2−メチル−5−(トリフルオロメチル)−4−[3−(トリメチルシリル)プロポキシ]フェニル}イミドホルムアミド、
O−[1−[(4−メトキシフェノキシ)メチル]−2,2−ジメチルプロピル] 1H−イミダゾール−1−カルボチオ酸、
2−アミノ−4−メチル−N−フェニル−5−チアゾールカルボキサミド、
2,4−ジヒドロ−5−メトキシ−2−メチル−4−[[[[1−[3−(トリフルオロメチル)フェニル]エチリデン]アミノ]オキシ]メチル]フェニル]−3H−1,2,3−トリアゾール−3−オン(CAS No.185336−79−2)、
N−(6−メトキシ−3−ピリジニル)シクロプロパンカルボキサミド。
ブロノポール、ジクロロフェン、ニトラピリン、ジメチルジチオカルバミン酸ニッケル、カスガマイシン、オクチリノン、フランカルボン酸、オキシテトラサイクリン、プロベナゾール、ストレプトマイシン、テクロフタラム、硫酸銅及び別の銅剤。
アセチルコリンエステラーゼ(AChE)阻害薬
カーバメート系、
例えば、アラニカルブ、アルジカルブ、アルドキシカルブ、アリキシカルブ、アミノカルブ、ベンジオカルブ、ベンフラカルブ、ブフェンカルブ、ブタカルブ、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、クロエトカルブ、ジメチラン、エチオフェンカルブ、フェノブカルブ、フェノチオカルブ、ホルメタネート、フラチオカルブ、イソプロカルブ、メタム−ナトリウム、メチオカルブ、メソミル、メトルカルブ、オキサミル、ピリミカーブ、プロメカルブ、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、トリアザメート;
有機リン酸エステル系、
例えば、アセフェート、アザメチホス、アジンホス(−メチル,−エチル)、ブロモホス−エチル、ブロムフェンビンホス(−メチル)、ブタチオホス、カズサホス、カルボフェノチオン、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(−メチル/−エチル)、クマホス、シアノフェンホス、シアノホス、クロルフェンビンホス、ジメトン−S−メチル、ジメトン−S−メチルスルホン、ジアリホス、ダイアジノン、ジクロフェンチオン、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、ジオキサベンゾホス、ダイスルホトン、EPN、エチオン、エトプロホス、エトリムホス、ファムフール、フェナミホス、フェニトロチオン、フェンスルホチオン、フェンチオン、フルピラゾホス、ホノホス、ホルモチオン、ホスメチラン、ホスチアゼート、ヘプテノホス、ヨードフェンホス、イプロベンホス、イサゾホス、イソフェンホス、O−サリチル酸イソプロピル、イソキサチオン、マラチオン、メカルバム、メタクリホス、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、オキシジメトン−メチル、パラチオン(−メチル/−エチル)、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、ホスホカルブ、ホキシム、ピリミホス(−メチル/−エチル)、プロフェノホス、プロパホス、プロペタムホス、プロチオホス、プロトエート、ピラクロホス、ピリダフェンチオン、ピリダチオン(pyridathion)、キナルホス、セブホス(sebufos)、スルホテップ、スルプロホス、テブピリムホス、テメホス、テルブホス、テトラクロロビンホス、チオメトン、トリアゾホス、トリクロルホン、バミドチオン;
ナトリウムチャンネルモジュレーター/電位依存性ナトリウムチャンネル遮断薬
ピレスロイド系、
例えば、アクリナトリン、アレスリン(d−シス−トランス,d−トランス)、ベータ−シフルトリン、ビフェントリン、ビオアレスリン、ビオアレスリン−S−シクロペンチル異性体、ビオエタノメトリン(bioethanomethrin)、ビオペルメトリン、ビオレスメトリン、クロバポルトリン(chlovaporthrin)、シス−シペルメトリン、シス−レスメトリン、シス−ペルメトリン、クロシトリン(clocythrin)、シクロプロトリン、シフルトリン、シハロトリン、シペルメトリン(アルファ−,ベータ−,シータ−,ゼータ−)、シフェノトリン、デルタメトリン、エムペントリン(1R−異性体)、エスフェンバレレート、エトフェンプロックス、フェンフルトリン(fenfluthrin)、フェンプロパトリン、フェンピリトリン、フェンバレレート、フルブロシトリネート(flubrocythrinate)、フルシトリネート、フルフェンプロックス、フルメトリン、フルバリネート、フブフェンプロックス(fubfenprox)、ガンマ−シハロトリン、イミプロトリン、カデトリン、ラムダ−シハロトリン、メトフルトリン、ペルメトリン(シス−,トランス−)、フェノトリン(1R−トランス−異性体)、プラレトリン、プロフルトリン、プロトリフェンブト(protrifenbute)、ピレスメトリン、レスメトリン、RU 15525、シラフルオフェン、タウ−フルバリネート、テフルトリン、テラレトリン、テトラメトリン(1R異性体)、トラロメトリン、トランスフルトリン、ZXI 8901、ピレトリン類(除虫菊(pyrethrum));
DDT;
オキサジアジン系、
例えば、インドキサカルブ;
セミカルバゾン系、
例えば、メタフルミゾン(BAS 3201);
アセチルコリン受容体作動薬/拮抗薬
クロロニコチニル系、
例えば、アセタミプリド、クロチアニジン、ジノテフラン、イミダクロプリド、ニテンピラム、ニチアジン、チアクロプリド、チアメトキサム;
ニコチン、ベンスルタップ、カルタップ;
アセチルコリン受容体モジュレーター
スピノシン系、
例えば、スピノサド;
GABA制御塩化物チャンネル拮抗薬
有機塩素系、
例えば、カンフェクロル、クロルダン、エンドスルファン、ガンマ−HCH、HCH、ヘプタクロル、リンダン、メトキシクロル;
フィプロール系、
例えば、アセトプロール、エチプロール、フィプロニル、ピラフルプロール、ピリプロール、バニリプロール;
塩化物チャンネル活性化剤
メクチン系、
例えば、アベルメクチン、エマメクチン、エマメクチン−安息香酸塩、イベルメクチン、レピメクチン、ミルベマイシン;
幼若ホルモンミメティクス
例えば、ジオフェノラン、エポフェノナン、フェノキシカルブ、ハイドロプレン、キノプレン、メトプレン、ピリプロキシフェン、トリプレン(triprene);
エクジソン作動薬/ディスラプター
ジアシルヒドラジン系、
例えば、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;
キチン生合成阻害薬
ベンゾイル尿素系、
例えば、ビストリフルロン、クロルフルアズロン(chlofluazuron)、ジフルベンズロン、フルアズロン、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、ペンフルロン(penfluron)、テフルベンズロン、トリフルムロン;
ブプロフェジン;
シロマジン;
酸化的リン酸化阻害薬、ATPディスラプター
ジアフェンチウロン;
有機スズ化合物、
例えば、アゾシクロチン、シヘキサチン、酸化フェンブタスズ;
H−プロトン勾配を遮断することにより作用する酸化的リン酸化デカップラー;
ピロール系、
例えば、クロルフェナピル;
ジニトロフェノール系、
例えば、ビナパクリル、ジノブトン、ジノカップ、DNOC、メプチルジノカップ(meptyldinocap);
Site−I 電子伝達阻害薬
METI系、
例えば、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;
ヒドラメチルノン;
ジコホル;
Site−II 電子伝達阻害薬
ロテノン;
Site−III 電子伝達阻害薬
アセキノシル、フルアクリピリム;
昆虫消化管膜の微生物ディスラプター
バシルス・ツリンギエンシス(Bacillus thuringiensis)株
脂質生合成阻害薬
テトロン酸系、
例えば、スピロジクロフェン、スピロメシフェン;
テトラミン酸系、
例えば、スピロテトラマト、シス−3−(2,5−ジメチルフェニル)−4−ヒドロキシ−8−メトキシ−1−アザスピロ[4.5]デク−3−エン−2−オン;
カルボキサミド系、
例えば、フロニカミド;
オクトパミン作用薬、
例えば、アミトラズ;
マグネシウム刺激ATPアーゼの阻害薬
プロパルギット;
ネライストキシン類似体、
例えば、チオシクラムシュウ酸水素塩(thiocyclam hydrogen oxalate)、チオスルタップ−ナトリウム(thiosultap-sodium);
リアノジン受容体作用薬
ベンゾジカルボキサミド系
例えば、フルベンジアミド;
アントラニルアミド系
例えば、リナキシピル(3−ブロモ−N−{4−クロロ−2−メチル−6−[(メチルアミノ)カルボニル]−フェニル}−1−(3−クロロピリジン−2−イル)−1H−ピラゾール−5−カルボキサミド);
生物学的薬剤、ホルモン又はフェロモン
アザジラクチン、バシルス属各種(Bacillus spec.)、ベアウベリア属各種(Beauveria spec.)、コドレモン(codlemone)、メタリジウム属各種(Metarrhizium spec.)、パエシロマイセス属各種(Paecilomyces spec.)、チューリンギエンシン(thuringiensin)、ベルチシリウム属各種(Verticillium spec.);
作用機序が知られていないか又は特定されていない活性化合物
燻蒸剤、
例えば、リン化アルミニウム、臭化メチル、フッ化スルフリル;
摂食阻害薬、
例えば、氷晶石(cryolite)、フロニカミド、ピメトロジン;
ダニ成長阻害薬、
例えば、クロフェンテジン、エトキサゾール、ヘキシチアゾクス;
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、ブロモプロピレート、ブプロフェジン、キノメチオネート、クロルジメホルム、クロロベンジレート、クロロピクリン、クロチアゾベン(clothiazoben)、シクロプレン(cycloprene)、シフルメトフェン、ジシクラニル、フェノキサクリム、フェントリファニル(fentrifanil)、フルベンジミン、フルフェネリム、フルテンジン(flutenzin)、ゴシプルレ(gossyplure)、ヒドラメチルノン、ジャポニルレ(japonilure)、メトキサジアゾン、石油、ピペロニルブトキシド、オレイン酸カリウム、ピリダリル、スルフラミド、テトラジホン、テトラスル、トリアラセン、ベルブチン(verbutin)。
アニリド系、例えば、ジフルフェニカン、及び、プロパニル;アリールカルボン酸系、例えば、ジクロロピコリン酸、ジカンバ、及び、ピクロラム;アリールオキシアルカン酸系、例えば、2,4−D、2,4−DB、2,4−DP、フルロキシピル、MCPA、MCPP、及び、トリクロピル;アリールオキシフェノキシアルカン酸エステル系、例えば、ジクロホップ−メチル、フェノキサプロップ−エチル、フルアジホップ−ブチル、ハロキシホップ−メチル、及び、キザロホップ−エチル;アジノン系、例えば、クロリダゾン、及び、ノルフルラゾン;カーバメート系、例えば、クロルプロファム、デスメディファム、フェンメディファム、及び、プロファム;クロロアセトアニリド系、例えば、アラクロール、アセトクロール、ブタクロール、メタザクロール、メトラクロール、プレチラクロール、及び、プロパクロール;ジニトロアニリン系、例えば、オリザリン、ペンジメタリン、及び、トリフルラリン;ジフェニルエーテル系、例えば、アシフルオルフェン、ビフェノックス、フルオログリコフェン、ホメサフェン、ハロサフェン、ラクトフェン、及び、オキシフルオルフェン;尿素系、例えば、クロルトルロン、ジウロン、フルオメツロン、イソプロツロン、リニュロン、及び、メタベンズチアズロン;ヒドロキシルアミン系、例えば、アロキシジム、クレトジム、シクロキシジム、セトキシジム、及び、トラルコキシジム;イミダゾリノン系、例えば、イマゼタピル、イマザメタベンズ、イマザピル、及び、イマザキン;ニトリル系、例えば、ブロモキシニル、ジクロベニル、及び、アイオキシニル;オキシアセトアミド系、例えば、メフェナセット;スルホニル尿素系、例えば、アミドスルフロン、ベンスルフロン−メチル、クロリムロン−エチル、クロルスルフロン、シノスルフロン、メトスルフロン−メチル、ニコスルフロン、プリミスルフロン、ピラゾスルフロン−エチル、チフェンスルフロン−メチル、トリアスルフロン、及び、トリベヌロン−メチル;チオカーバメート系、例えば、ブチレート、シクロエート、ジアレート、EPTC、エスプロカルブ、モリネート、プロスルホカルブ、チオベンカルブ、及び、トリアレート;トリアジン系、例えば、アトラジン、シアナジン、シマジン、シメトリン、テルブトリン、及び、テルブチラジン;トリアジノン系、例えば、ヘキサジノン、メタミトロン、及び、メトリブジン;その他、例えば、アミノトリアゾール、4−アミノ−N−(1,1−ジメチルエチル)−4,5−ジヒドロ−3−(1−メチルエチル)−5−オキソ−1H−1,2,4−トリアゾール−1−カルボキサミド、ベンフレセート、ベンタゾン、シンメチリン、クロマゾン、クロピラリド、ジフェンゾコート、ジチオピル、エトフメセート、フルオロクロリドン、グルホシネート、グリホセート、イソキサベン、ピリデート、キンクロラック、キンメラック、スルホサート、及び、トリジファン。
Rは、4〜20個の炭素原子を有する直鎖又は分枝鎖のアルキルを表し;
R’は、H、メチル、エチル、n−プロピル、イソプロピル、n−ブチル、イソブチル、t−ブチル、n−ペンチル又はn−ヘキシルを表し;
AOは、エチレンオキシドラジカル、プロピレンオキシドラジカル又はブチレンオキシドラジカルを表すか、又は、エチレンオキシドラジカルとプロピレンオキシドラジカルの混合物を表すか、又は、エチレンオキシドラジカルとブチレンオキシドラジカルの混合物を表し;
mは、2〜30の数字を表す]
で表されるアルカノールアルコキシレートである。
クチクラのレベルで浸透促進剤として作用する添加剤は、以下では促進添加剤(accelerator additive)と称し得る(cf. Schonherr and Baur, 1994, Pesticide Science 42, 185-208)。促進添加剤の特徴は、水性散布液から及び/又は散布被膜からクチクラ内に浸透し、それによって、当該活性化合物のクチクラ内への移動性を増大させるそれらの能力である。それに反して、ポリエチレングリコールなどの別の添加剤は、散布被膜(液相による)上でのみ作用するか、又は、湿潤剤としてのみ作用する(例えば、ドデシル硫酸ナトリウム)。
保持は、散布による施用後における、散布されたミストの表面(例えば、植物又は植物の一部(葉))への付着を意味するものと理解される。そのような保持は、散布液の組成と処理された表面の特性の両方に依存する。
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EA (1) | EA014782B1 (ja) |
ES (1) | ES2544857T3 (ja) |
MX (1) | MXPA08003197A (ja) |
PH (1) | PH12008500597A1 (ja) |
PL (1) | PL1926369T3 (ja) |
TW (1) | TW200731925A (ja) |
UA (1) | UA90342C2 (ja) |
WO (1) | WO2007028538A2 (ja) |
ZA (1) | ZA200802072B (ja) |
Cited By (1)
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JP2019504023A (ja) * | 2015-12-22 | 2019-02-14 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 親油性化合物の乳剤 |
Families Citing this family (13)
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IL148684A (en) * | 2002-03-14 | 2006-12-31 | Yoel Sasson | Pesticidal composition |
DE102005042876A1 (de) | 2005-09-09 | 2007-03-22 | Bayer Cropscience Ag | Verwendung von Laktatestern zur Verbesserung der Wirkung von Pflanzenschutzmitteln |
AR062587A1 (es) | 2006-08-30 | 2008-11-19 | Dow Agrosciences Llc | Composiciones agricolamente utiles |
DE102007018983A1 (de) * | 2007-04-21 | 2008-10-23 | Cognis Ip Management Gmbh | Agrochemische Zubereitungen |
MX2011000806A (es) * | 2008-07-24 | 2011-03-15 | Bayer Cropscience Ag | Espesante para concentrados compatibles con plantas, dispersables en agua. |
EA020385B1 (ru) * | 2009-07-28 | 2014-10-30 | Басф Се | Пестицидные суспоэмульсионные композиции |
US20110201500A1 (en) * | 2010-02-12 | 2011-08-18 | Basf Se | Anhydrous Composition Comprising a Dissolved and a Suspended Pesticide, Alkyl Lactate and Alcohol |
TR201802433T4 (tr) | 2010-02-12 | 2018-03-21 | Basf Se | Çözülmüş ve süspansiyon yapılmış bir pestisit, alkillaktat ve alkol içeren susuz bir bileşim. |
BR112012023044A2 (pt) | 2010-03-12 | 2016-08-30 | Monsanto Technology Llc | composições para saúde de planta compreendendo um pesticida solúvel em água e um agroquímico insolúvel em água. |
BR112014001917A2 (pt) | 2011-07-26 | 2017-02-21 | Bayer Ip Gmbh | ésteres de lactato eterificados, processos para a sua produção e seu uso para melhorar o efeito de agentes para proteger plantas |
WO2015121119A1 (en) * | 2014-02-14 | 2015-08-20 | BASF Agro B.V. | Emulsifiable concentrate comprising pesticide, alkyl lactate, and lactamide |
US10785973B2 (en) | 2014-09-02 | 2020-09-29 | Basf Se | Aqueous pesticide microemulsion |
CN110235892A (zh) * | 2019-07-10 | 2019-09-17 | 四川国光农化股份有限公司 | 一种赤霉酸可溶液剂及其制备方法 |
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2005
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2006
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- 2006-08-31 KR KR1020087007966A patent/KR20080044898A/ko active IP Right Grant
- 2006-08-31 ES ES06791755.9T patent/ES2544857T3/es active Active
- 2006-08-31 JP JP2008529514A patent/JP5188974B2/ja active Active
- 2006-08-31 CN CN2006800331972A patent/CN101262761B/zh active Active
- 2006-08-31 UA UAA200804511A patent/UA90342C2/ru unknown
- 2006-08-31 EA EA200800777A patent/EA014782B1/ru not_active IP Right Cessation
- 2006-08-31 PL PL06791755T patent/PL1926369T3/pl unknown
- 2006-08-31 EP EP06791755.9A patent/EP1926369B1/de not_active Revoked
- 2006-08-31 US US12/066,040 patent/US20080318791A1/en not_active Abandoned
- 2006-08-31 CA CA2621633A patent/CA2621633C/en not_active Expired - Fee Related
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- 2006-09-07 AR ARP060103896A patent/AR056502A1/es not_active Application Discontinuation
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2008
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JP2019504023A (ja) * | 2015-12-22 | 2019-02-14 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 親油性化合物の乳剤 |
Also Published As
Publication number | Publication date |
---|---|
MXPA08003197A (es) | 2008-03-19 |
EA200800777A1 (ru) | 2008-10-30 |
US20080318791A1 (en) | 2008-12-25 |
WO2007028538A2 (de) | 2007-03-15 |
CA2621633A1 (en) | 2007-03-15 |
AU2006289348A1 (en) | 2007-03-15 |
BRPI0615648B1 (pt) | 2016-07-12 |
UA90342C2 (ru) | 2010-04-26 |
DE102005042876A1 (de) | 2007-03-22 |
MX290705B (ja) | 2011-10-04 |
EP1926369B1 (de) | 2015-06-17 |
CA2621633C (en) | 2015-01-06 |
KR20080044898A (ko) | 2008-05-21 |
WO2007028538A3 (de) | 2007-05-31 |
ES2544857T3 (es) | 2015-09-04 |
EA014782B1 (ru) | 2011-02-28 |
CN101262761A (zh) | 2008-09-10 |
TW200731925A (en) | 2007-09-01 |
AR056502A1 (es) | 2007-10-10 |
JP5188974B2 (ja) | 2013-04-24 |
ZA200802072B (en) | 2009-08-26 |
PH12008500597A1 (en) | 2013-01-28 |
AU2006289348B2 (en) | 2011-04-21 |
CN101262761B (zh) | 2012-02-29 |
EP1926369A2 (de) | 2008-06-04 |
BRPI0615648A2 (pt) | 2011-05-24 |
PL1926369T3 (pl) | 2015-11-30 |
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