JP2009051834A - 効果に優れる農薬組成物 - Google Patents
効果に優れる農薬組成物 Download PDFInfo
- Publication number
- JP2009051834A JP2009051834A JP2008200509A JP2008200509A JP2009051834A JP 2009051834 A JP2009051834 A JP 2009051834A JP 2008200509 A JP2008200509 A JP 2008200509A JP 2008200509 A JP2008200509 A JP 2008200509A JP 2009051834 A JP2009051834 A JP 2009051834A
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- Prior art keywords
- generic name
- composition according
- agrochemical composition
- name
- alkyl
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 33
- 230000000694 effects Effects 0.000 title description 11
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 52
- 239000004480 active ingredient Substances 0.000 claims abstract description 33
- 239000004094 surface-active agent Substances 0.000 claims abstract description 32
- 239000012752 auxiliary agent Substances 0.000 claims abstract description 11
- 239000003093 cationic surfactant Substances 0.000 claims abstract description 11
- 239000002736 nonionic surfactant Substances 0.000 claims abstract description 9
- 125000001424 substituent group Chemical group 0.000 claims abstract description 8
- 239000003960 organic solvent Substances 0.000 claims abstract description 5
- 239000003945 anionic surfactant Substances 0.000 claims abstract description 4
- 239000012872 agrochemical composition Substances 0.000 claims description 39
- -1 alkyl glycoside Chemical class 0.000 claims description 38
- 230000002363 herbicidal effect Effects 0.000 claims description 27
- 239000003905 agrochemical Substances 0.000 claims description 18
- 150000003839 salts Chemical class 0.000 claims description 18
- 150000001413 amino acids Chemical class 0.000 claims description 13
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
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- 125000005210 alkyl ammonium group Chemical group 0.000 claims description 10
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
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- ATROHALUCMTWTB-OWBHPGMISA-N phoxim Chemical compound CCOP(=S)(OCC)O\N=C(\C#N)C1=CC=CC=C1 ATROHALUCMTWTB-OWBHPGMISA-N 0.000 description 1
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- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- RWPGFSMJFRPDDP-UHFFFAOYSA-L potassium metabisulfite Chemical compound [K+].[K+].[O-]S(=O)S([O-])(=O)=O RWPGFSMJFRPDDP-UHFFFAOYSA-L 0.000 description 1
- 235000010263 potassium metabisulphite Nutrition 0.000 description 1
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- 150000003138 primary alcohols Chemical class 0.000 description 1
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Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
【解決手段】 農薬活性成分および式(1):HOR1R3C−[CH2]n−CR2R4OH〔式中、R1およびR2は独立に炭素原子3〜6個を有するアルキル基の群から選ばれる置換基であり、R3およびR4は独立に炭素原子1〜2個を有するアルキル基であり、nは1〜6の整数である。〕で表される界面活性剤を含む農薬組成物。当該農薬組成物は更に補助剤を含むことができ、該補助剤としてはカチオン性界面活性剤、アニオン性界面活性剤、ノニオン性界面活性剤および有機溶剤が好ましい。
【選択図】 なし
Description
ウィード サイエンス(Weed Science)、1977年、第25巻、p.275−287
HOR1R3C−[CH2]n−CR2R4OH (1)
〔式中、R1およびR2は、独立に炭素原子3〜6個を有するアルキル基の群から選ばれる置換基であり、R3およびR4は独立に炭素原子1〜2個を有するアルキル基であり、nは1〜6の整数である。〕で表される界面活性剤を含む農薬組成物。
R20O(R21O)b(G)a (2)
〔式中、
R20はC6〜30アルキル基、C6〜30アルケニル基、C6〜30アルキニル基またはC6〜30アルキルフェニル基を表し、
R21はC2〜4アルキレン鎖を表し、
Gは5単糖残基または6単糖残基を表し、
bは0ないし12の数値を表し、
aは1ないし10の数値を表す。〕で表される。
式(2)において、Gがグルコース残基でありbが0であるアルキルポリグリコシド、
式(2)において、R20がC6〜30アルキル基またはC6〜30アルケニル基であるアルキルポリグリコシド、
式(2)において、R20がC6、C8、C10、C12、C14、C16もしくはC18の鎖長を有するアルキル基、またはC6、C8、C10、C12、C14、C16もしくはC18の鎖長を有するアルケニル基であるアルキルポリグリコシド、およびそれらの混合物からなるアルキルポリグリコシド、
式(2)において、(G)aがグリコシド結合により互いに結合している平均1ないし10個の糖残基であるアルキルポリグリコシド、
式(2)において、(G)aは異なった種類の還元糖の糖残基で構成されていてもよく、その糖残基がグルコースまたはマルトースであるアルキルポリグリコシド、および
式(2)において、糖残基の数を表しているaは典型的な分布に基づく統計的平均値であり、特に適切なものはアルキル基当たり平均1ないし5個の糖分子を含み、より好ましくは、1ないし5個のグルコース残基を含み、特に好ましくは、少なくとも1アルキルポリグリコシドの平均グリコシド残基重合度が約1ないし約1.8であり、これらの界面活性剤のうち、特にさらに好ましくはC6〜14の鎖長のアルキル基を有するアルキルポリグリコシドが挙げられる。
1.四級化長鎖アミン:
a)アルキルトリ(低級アルキル)アンモニウム塩化物
i)トリメチルココアンモニウム塩化物(ココ:C12〜15アルキル)
ii)トリメチルオクタデシルアンモニウム塩化物
b)ジアルキルジ(低級アルキル)アンモニウム塩化物
i)ジメチルジオクタデシルアンモニウム塩化物
2.四級化ポリオキシアルキレン長鎖アミン:
a)ジアルキルジ(ヒドロキシエチル)アンモニウム塩化物
i)メチルビス(2−ヒドロキシエチル)ココアンモニウム塩化物
ii)メチルビス(2−ヒドロキシエチル)ラウリルアンモニウム塩化物
iii)メチルビス(2−ヒドロキシエチル)オレイルアンモニウム塩化物
b)アルキルジ(ポリオキシエチレン)低級アルキルアンモニウム塩化物
i)メチルビス(ω−ヒドロキシポリオキシエチレン)ココアンモニウム塩化物(ただし、ポリオキシエチレンは3モル〜20モルのエチレンオキシドから誘導される)
ii)メチルビス(ω−ヒドロキシポリオキシエチレン)オレイルアンモニウム塩化物(ただし、ポリオキシエチレンは3モル〜20モルのエチレンオキシドから誘導される)
c)ヒドロキシアルキルポリオキシエチレンジ(低級アルキル)アンモニウム塩化物
i)ヒドロキシエチルジメチルポリオキシエチレン(2モル)アンモニウム塩化物
d)アルキルトリ(ポリオキシエチレン)アンモニウムホスフェート
i)ラウリルトリポリオキシエチレンアンモニウムホスフェート
3.四級化ピリジン類:
i)N−オクチルピリジン塩化物
ii)N−ドデシルピリジン塩化物
4.四級化されたカルボキシル化イミダゾリン類(閉鎖および開鎖):
i)N−カルボキシメチル−N−アミノエチルウンデシルイミダゾリン
ii)N−カルボキシ−N−ヒドロキシエチルウンデシルイミダゾリン
iii)N−カルボキシメチル−N−アミノエチル−(N’,N’−ジカルボキシメチル)ウンデシルイミダゾリン
iv)N−カルボキシメチル−N−(カルボキシメトキシ)エチルウンデシルイミダゾリン
v)N−カルボキシメチル−N−ヒドロキシエチルヘプタデシルイミダゾリン
vi)N−カルボキシメチル−N−ヒドロキシエチルウンデシルイミダゾリン
5.トリアルキルベタイン:
a)アルキルジ(低級アルキル)ベタイン
i)ラウリルジメチルベタイン
ii)ステアリルジメチルベタイン
iii)ココジメチルベタイン
iv)デシルジメチルベタイン
6.アミンオキシド:
a)アルキルジ(低級アルキル)アミンオキシド
i)ラウリルジメチルアミンオキシド
ii)ステアリルジメチルアミンオキシド
b)ジ(ヒドロキシエチル)アルキルアミンオキシド
i)ジ(ヒドロキシエチル)オクチルアミンオキシド
ii)ジ(ヒドロキシエチル)ドデシルアミンオキシド
iii)ジ(ヒドロキシエチル)タロウアミンオキシド
c)ジ(ポリヒドロキシエチレン)アルキルアミンオキシド
i)ビス(ω−ヒドロキシポリオキシエチレン)タロウアミンオキシド
d)低級アルキルポリオキシエチレンアルキルアミンオキシド
i)メチルポリオキシエチレン(2モル)ココアミンオキシド。
プラスチック製の5寸鉢に殺菌した洪積土壌を入れ、スギナの塊茎、ワルナスビの根茎を埋め込み、またはツユクサ、セイヨウタンポポ、ノボロギク、イヌホウズキの種子を播種し、約1.5cm覆土した後、25℃の温室内において植物を育成した。スギナは30日間、その他の草種は20日〜30日間育成した。第1表に示した組成物を第2表に示した希釈倍率に水で希釈して散布液を調製し、50L/10aの割合で茎葉部へ小型スプレーで均一に処理した。
Claims (18)
- 農薬活性成分および式(1):
HOR1R3C−[CH2]n−CR2R4OH (1)
〔式中、R1およびR2は、独立に炭素原子3〜6個を有するアルキル基の群から選ばれる置換基であり、R3およびR4は独立に炭素原子1〜2個を有するアルキル基であり、nは1〜6の整数である。〕で表される界面活性剤を含む農薬組成物。 - 農薬活性成分が、除草活性成分である請求項1記載の農薬組成物。
- 除草活性成分が、アミノ酸系除草活性成分である請求項2記載の農薬組成物。
- アミノ酸系除草活性成分がグリホサート、ビアラホスおよびグルホシネート並びにそれらの塩から選ばれる1種以上である請求項3記載の農薬組成物。
- アミノ酸系除草活性成分がグリホサートおよびその塩から選ばれる1種以上である請求項3記載の農薬組成物。
- 更に補助剤を含有する請求項1ないし5から選ばれるいずれか1項記載の農薬組成物。
- 補助剤が、カチオン性界面活性剤、アニオン性界面活性剤、ノニオン性界面活性剤および有機溶剤から選ばれる1種以上である請求項6記載の農薬組成物。
- 補助剤がカチオン性界面活性剤である請求項6記載の農薬組成物。
- 補助剤がノニオン性界面活性剤である請求項6記載の農薬組成物。
- カチオン性界面活性剤が四級アルキルアンモニウム塩である請求項8記載の農薬組成物。
- ノニオン性界面活性剤がアルキルグリコシドまたはアルキルポリグリコシドである請求項9記載の農薬組成物。
- 式(1)において、R1およびR2が独立に炭素原子4〜6個を有するアルキル基の群から選ばれる置換基である請求項1ないし11から選ばれるいずれか1項記載の農薬組成物。
- 式(1)において、R3およびR4がメチル基である請求項1ないし11から選ばれるいずれか1項記載の農薬組成物。
- nが1〜4の整数である請求項1ないし11から選ばれるいずれか1項記載の農薬組成物。
- nが2である請求項1ないし11から選ばれるいずれか1項記載の農薬組成物。
- R1およびR2が独立に炭素原子4〜6個を有するアルキル基の群から選ばれる置換基であり、R3およびR4がメチル基であり、そしてnが2である請求項1ないし11から選ばれるいずれか1項記載の農薬組成物。
- 式(1)で表される界面活性剤が2,4,7,9−テトラメチルデカン−4,7−ジオールである請求項1ないし11から選ばれるいずれか1項記載の農薬組成物。
- 式(1)で表される界面活性剤が2,5,8,11−テトラメチルドデカン−5,8−ジオールである請求項1ないし11から選ばれるいずれか1項記載の農薬組成物。
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