JP4986023B2 - 植物病害防除剤組成物 - Google Patents
植物病害防除剤組成物 Download PDFInfo
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- JP4986023B2 JP4986023B2 JP2006277377A JP2006277377A JP4986023B2 JP 4986023 B2 JP4986023 B2 JP 4986023B2 JP 2006277377 A JP2006277377 A JP 2006277377A JP 2006277377 A JP2006277377 A JP 2006277377A JP 4986023 B2 JP4986023 B2 JP 4986023B2
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- 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
- 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
- JARYYMUOCXVXNK-IMTORBKUSA-N validamycin 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-IMTORBKUSA-N 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000004552 water soluble powder Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 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
Landscapes
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
ルクロホスメチル(tolclofos-methyl)、トリルフラニド(tolylfluanid)、トリアジメホン(triadimefon)、トリアジメノール(toriadimenol)、トリアゾキシド(triazoxide)、トリシクラゾール(tricyclazole)、トリデモルフ(tridemorph)、トリフルミゾール(triflumizole)、トリホリン(triforine)、トリチコナゾール(triticonazole)、テーシーエムテービー(TCMTB)、テクロフタラム(tecloftalam)、テコラム(tecoram)、チアジフルア(thiadifluor)、チシオフェン(thicyofen)、チオクロルフェンフィム(thiochlorfenphim)、チオメルサム(thiomersal)、チオファネイト(thiophanate)、チオキノックス(thioquinox)、チアジニル(tiadinil)、チオキシミド(tioxymid)、トリマーキュリアセテイト(tolylmercury acetate)、トリアミフォス(triamiphos)、トリアリモル(triarimol)、トリアズブチル(triazbutil)、トリブチルチンオキサイド(tributyltin oxide)、トリクルアミド(trichlamide)、トリフロキシストロビン(trifloxystrobin)、バリダマイシン(validamycin)、ビンクロゾリン(vinclozolin)、硫酸亜鉛(zinc sulfate)、ジネブ(zineb)、ジラム(ziram)、ゾキサミド(zoxamide)、ザリルアミド(zarilamid)、ジンクナフテネイト(zinc naphthenate)、エクロメゾール、及びシイタケ菌糸体抽出物。
カープレックス80−D(デグサ社製)2.00重量部、グリセリンRG(商品名、グリセリン、日本油脂(株)製)1.00重量部を計量し混合した。続いて、みやきDLクレー(商品名、クレー、(株)三養基興業所製)10.00重量部、化合物Aジェット粉砕品(98.8%、平均粒子径1.9μm)0.56重量部を添加し混合した。さらにみやきDLクレー86.44重量部を混合後、ロータースピードミルP−14型(フリッチュ・ジャパン(株)製)にて全量粉砕混合して化合物Aを0.5%含有する粉剤を得た。
カープレックス80−D2.00重量部、グリセリンRG2.00重量部を計量し混合した。続いて、みやきDLクレー10.00重量部、化合物Aジェット粉砕品(98.8%、平均粒子径1.9μm)0.56重量部を添加し混合した。さらにみやきDLクレー85.44重量部を混合後、ロータースピードミルP−14型にて全量粉砕混合して化合物Aを0.5%含有する粉剤を得た。
カープレックス80−D2.00重量部、グリセリンRG3.00重量部を計量し混合した。続いて、みやきDLクレー10.00重量部、化合物Aジェット粉砕品(98.8%、平均粒子径1.9μm)0.56重量部を添加し混合した。さらにみやきDLクレー84.44重量部を混合後、ロータースピードミルP−14型にて全量粉砕混合して化合物Aを0.5%含有する粉剤を得た。
グリセリンRGをニューサイザー510R(商品名、エポキシ化大豆油、日本油脂(株)製)に置き換えた以外は実施例1に従い、化合物Aを0.5%含有する粉剤を得た。
グリセリンRGをエピオールG−100(商品名、グリシジルエーテル、日本油脂(株)製)に置き換えた以外は実施例1に従い、化合物Aを0.5%含有する粉剤を得た。
グリセリンRGをエピオールEH(商品名、グリシジルエーテル、日本油脂(株)製)に置き換えた以外は実施例1に従い、化合物Aを0.5%含有する粉剤を得た。
グリセリンRGをディクスゾール600(商品名、イソプロピルリン酸エステル(PAP)、第一工業製薬製)に置き換えた以外は実施例1に従い、化合物Aを0.5%含有する粉剤を得た。
グリセリンRGをドリレスB(商品名、三共(株)製)に置き換えた以外は実施例1に従い、化合物Aを0.5%含有する粉剤を得た。
グリセリンRGをジエチレングリコールに置き換えた以外は実施例1に従い、化合物Aを0.5%含有する粉剤を得た。
みやきDLクレー((株)三養基興業所製)13.00重量部、化合物Aジェット粉砕品(98.8%、平均粒子径1.9μm)0.56重量部を添加し混合した。さらにみやきDLクレー86.44重量部を混合後、ロータースピードミルP−14型(フリッチュ・ジャパン(株)製)にて全量粉砕混合して化合物Aを0.5%含有する粉剤を得た。
実施例1〜9および比較例で製造した粉剤を、50℃下で10日間または1月間、苛酷保存した後、粉剤中の化合物Aの含量を高速液体クロマトグラフィーにて測定し、化合物Aの分解率(%)を次式で算出した。
化合物Aの分解率(%)=(初期含量−苛酷保存後含量)/初期含量×100
なお、0℃にて保存した粉剤中の化合物Aの含量を、過酷保存した粉剤中の化合物Aの含量測定時に測定し、その値を化合物Aの初期含量とした。結果を表1に示した。
――――――――――――――――――――――――――
化合物Aの分解率(%)
――――――――――――――――――――――――――
50℃10日 50℃1ヶ月
――――――――――――――――――――――――――
実施例1 3.2 −
実施例2 1.5 −
実施例3 1.9 −
実施例4 2.0 −
実施例5 2.0 −
実施例6 3.2 −
実施例7 5.0 −
実施例8 5.0 −
実施例9 − 3.1
比較例 9.5 −
――――――――――――――――――――――――――
Claims (2)
- (a)補助剤としてグリセリン、エポキシ化植物油、および1価または多価アルコールの水酸基に2,3−エポキシプロパノールが一個以上エーテル結合したグリシジルエーテルからなる群から選ばれる1種以上、並びに(b)農薬活性成分として3−(3−ブロモ−6−フルオロ−2−メチルインドール−1−イルスルホニル)−N,N−ジメチル−1H−1,2,4−トリアゾール−1−スルホンアミドを含有することを特徴とする植物病害防除剤組成物。
- (a)補助剤としてグリセリン、エポキシ化植物油、および1価または多価アルコールの水酸基に2,3−エポキシプロパノールが一個以上エーテル結合したグリシジルエーテルからなる群から選ばれる1種以上、並びに(b)農薬活性成分として3−(3−ブロモ−6−フルオロ−2−メチルインドール−1−イルスルホニル)−N,N−ジメチル−1H−1,2,4−トリアゾール−1−スルホンアミドを組合せて用いることを特徴とする該農薬活性成分の分解防止方法。
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