JPS61218503A - Herbicidal composition - Google Patents
Herbicidal compositionInfo
- Publication number
- JPS61218503A JPS61218503A JP6045485A JP6045485A JPS61218503A JP S61218503 A JPS61218503 A JP S61218503A JP 6045485 A JP6045485 A JP 6045485A JP 6045485 A JP6045485 A JP 6045485A JP S61218503 A JPS61218503 A JP S61218503A
- Authority
- JP
- Japan
- Prior art keywords
- parts
- lower alkyl
- product name
- herbicidal composition
- water
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 20
- 239000000203 mixture Substances 0.000 title claims abstract description 20
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 12
- 239000000126 substance Substances 0.000 claims abstract description 12
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims abstract description 10
- VMFDZAIIYSKZDE-UHFFFAOYSA-N 1h-pyrazol-5-ylsulfonylurea Chemical class NC(=O)NS(=O)(=O)C=1C=CNN=1 VMFDZAIIYSKZDE-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 3
- 239000004480 active ingredient Substances 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- ZBMRKNMTMPPMMK-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid;azane Chemical compound [NH4+].CP(O)(=O)CCC(N)C([O-])=O ZBMRKNMTMPPMMK-UHFFFAOYSA-N 0.000 claims 1
- DEFJQIDDEAULHB-IMJSIDKUSA-N L-alanyl-L-alanine Chemical compound C[C@H](N)C(=O)N[C@@H](C)C(O)=O DEFJQIDDEAULHB-IMJSIDKUSA-N 0.000 claims 1
- 108010056243 alanylalanine Proteins 0.000 claims 1
- -1 amino-4-methylphosphinobutyryl Chemical group 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 24
- 241000196324 Embryophyta Species 0.000 abstract description 15
- IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 abstract description 7
- 239000005561 Glufosinate Substances 0.000 abstract description 7
- 239000005562 Glyphosate Substances 0.000 abstract description 7
- 229940097068 glyphosate Drugs 0.000 abstract description 7
- 230000002195 synergetic effect Effects 0.000 abstract description 6
- GINJFDRNADDBIN-FXQIFTODSA-N bilanafos Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCP(C)(O)=O GINJFDRNADDBIN-FXQIFTODSA-N 0.000 abstract 2
- JEAPVUQLKCFPOM-JVIMKECRSA-N (2s)-2-[[(2s)-2-[(2-amino-4-methylphosphanylbutyl)amino]propanoyl]amino]propanoic acid Chemical compound CPCCC(N)CN[C@@H](C)C(=O)N[C@@H](C)C(O)=O JEAPVUQLKCFPOM-JVIMKECRSA-N 0.000 abstract 1
- CZNHDJGFEWSIKB-UHFFFAOYSA-N NC(CCCO[PH2]=O)C(O)=O.N Chemical compound NC(CCCO[PH2]=O)C(O)=O.N CZNHDJGFEWSIKB-UHFFFAOYSA-N 0.000 abstract 1
- 239000000470 constituent Substances 0.000 abstract 1
- 230000009969 flowable effect Effects 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 239000004009 herbicide Substances 0.000 description 15
- 239000003795 chemical substances by application Substances 0.000 description 9
- 239000003945 anionic surfactant Substances 0.000 description 8
- 239000002736 nonionic surfactant Substances 0.000 description 8
- 239000002562 thickening agent Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 239000002689 soil Substances 0.000 description 5
- 240000001341 Reynoutria japonica Species 0.000 description 3
- 235000018167 Reynoutria japonica Nutrition 0.000 description 3
- 230000005764 inhibitory process Effects 0.000 description 3
- 244000025254 Cannabis sativa Species 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- XHDOGGABNYYANU-WPZUCAASSA-N (2s)-2-[[(2s)-2-[(2-amino-4-methylphosphanylbutanoyl)amino]propanoyl]amino]propanoic acid Chemical compound CPCCC(N)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(O)=O XHDOGGABNYYANU-WPZUCAASSA-N 0.000 description 1
- 240000001592 Amaranthus caudatus Species 0.000 description 1
- 235000009328 Amaranthus caudatus Nutrition 0.000 description 1
- 240000001549 Ipomoea eriocarpa Species 0.000 description 1
- 235000005146 Ipomoea eriocarpa Nutrition 0.000 description 1
- 241001363516 Plusia festucae Species 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002547 new drug Substances 0.000 description 1
- 239000002420 orchard Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は一般式(■):
C式中角は低級アルキル基を示す。Bは水素原子または
低級アルキル基を示す。Rは低級アルキル基を示す。X
およびYはそれぞれ独立して、低級アルキル基または低
級アルコキシ基を示す。〕
で表されるピラゾールスルホニルウレア誘導体とN−ホ
スホノメチルグリシン(以下グリホセートと称する。)
、アンモニウム−(3−アミノカルボキシプロビル)−
メチルホスフィネート(以下グルホシネートと称する。DETAILED DESCRIPTION OF THE INVENTION The present invention is based on the general formula (■): The middle angle in the formula C represents a lower alkyl group. B represents a hydrogen atom or a lower alkyl group. R represents a lower alkyl group. X
and Y each independently represent a lower alkyl group or a lower alkoxy group. ] Pyrazolesulfonylurea derivative represented by and N-phosphonomethylglycine (hereinafter referred to as glyphosate).
, ammonium-(3-aminocarboxyprobyl)-
Methylphosphinate (hereinafter referred to as glufosinate).
)または(2−アミノ−4−メチルホスフィノブチリル
)アラニルアラニンのうち(以下ビアラフオスと称する
。)のうちの1種とを有効成分として含有することを特
徴とする除草剤組成物に関する。) or (2-amino-4-methylphosphinobutyryl)alanylalanine (hereinafter referred to as bialafuos) as an active ingredient.
長年にわたる除草剤の研究開発のなかから多種多様な薬
剤が実用化され、これら除草剤は雑草防除作業の省力化
や農園芸作物の生産性向上に寄与してきた。今日におい
ても、より優れた除草特性を有する新規薬剤の開発が要
望されている。As a result of many years of research and development into herbicides, a wide variety of herbicides have been put into practical use, and these herbicides have contributed to labor-saving weed control operations and improved productivity of agricultural and horticultural crops. Even today, there is a demand for the development of new drugs with better herbicidal properties.
一般式(1)で表される化合物は従来の除草剤に比して
非常に低薬量で優れた除草効果をあげるが本発明者は、
前記一般式(1)で表される化合物の除草効果を増大さ
せるべく研究を行った結果、一般式(1)で表される化
合物に、従来使用されている前記除草剤を配合すると、
それぞれの除草効果が単に相加的にえられるのみならず
、相乗的殺草効果が現れる事を見出し本発明を完成した
。The compound represented by the general formula (1) has excellent herbicidal effects at a very low dose compared to conventional herbicides, but the present inventors
As a result of conducting research to increase the herbicidal effect of the compound represented by the general formula (1), it was found that when the compound represented by the general formula (1) is blended with the conventionally used herbicide,
The present invention was completed by discovering that the herbicidal effects of each species are not only additive, but also synergistic.
この相乗効果は大きく、本発明組成物により、低薬量で
一年生雑草から多年生雑草まで完全に防除でき、本発明
の有用性は非常に大きい。This synergistic effect is great, and the composition of the present invention can completely control both annual and perennial weeds with a low dose, making the present invention extremely useful.
本発明除草剤組成物は、雑草の発芽前および発芽後に処
理しても効果を有し、土壌処理、茎葉兼土壌処理でも高
い効果が得られる。畑地、果°樹園などの農園芸分野及
び運動場、空き地、林地、タンクヤード、線路端などの
非農耕地における各種雑草の防除にも適用でき、雑草防
除にあたって大きな経済的効果を示す。The herbicide composition of the present invention is effective even when treated before and after weed germination, and is highly effective when treated in soil or in foliage and soil treatment. It can also be applied to control various weeds in agricultural and horticultural fields such as fields and orchards, as well as non-agricultural lands such as playgrounds, vacant lots, forest areas, tank yards, and railway edges, and shows great economic effects in weed control.
本発明による組成物は、各成分の相対的活性にもよるが
、一般にはグリホセート、グルホシネートまたはピアラ
フオス1重量部当たり一般式(1)で表される化合物0
.0001〜50重量部、好適には0.001〜10重
量部含んでいる。多くの場合、本発明の配合除草剤の最
高の利点は式(I)で表される化合物の割合が他の除草
剤よりも比較的低い時、例えば他の除草剤1重量部当た
り一般式(1)で表される化合物が0.001〜0.1
重量部のときに得られる。The composition according to the present invention generally contains 0% of the compound represented by the general formula (1) per part by weight of glyphosate, glufosinate or pialaf ox, depending on the relative activity of each component.
.. 0001 to 50 parts by weight, preferably 0.001 to 10 parts by weight. In many cases, the greatest advantage of the combined herbicides of the invention is when the proportion of compounds of formula (I) is relatively low compared to other herbicides, e.g. The compound represented by 1) is 0.001 to 0.1
Obtained when parts by weight.
適用すべき混合物の量は、多数の因子、例えば生育を阻
止すべき特定の対象植物の種類などにより左右されるが
、一般にo、ooi〜10Kg/haの量が普通は適当
である。当業者であれば標準化された通常のテストによ
り特に多数の実験を行わなくても適当な使用割合が容易
に決定出来る。The amount of mixture to be applied will depend on a number of factors, such as the particular species of target plant to be inhibited, but in general amounts from 0.00 to 10 Kg/ha are usually suitable. Those skilled in the art can readily determine appropriate usage rates by routine, standardized tests without the need for extensive experimentation.
本発明組成物は、活性成分を固体または液体希釈剤から
なるキャリヤーと混合した組成物の形態で使用するのが
好ましい。組成物は更に界面活性剤を含むのが好ましい
。The compositions of the invention are preferably used in the form of a composition in which the active ingredient is mixed with a carrier consisting of a solid or liquid diluent. Preferably, the composition further comprises a surfactant.
次ぎに本発明における一般式(I)で表される化合物の
代表例を第1表に示す。以下の化合物は一般式(1)で
表される化合物に包含されるものではあるが、一般式(
I)で表される化合物はこれらに限定されるものではな
い。Next, Table 1 shows representative examples of the compounds represented by the general formula (I) in the present invention. Although the following compounds are included in the compounds represented by the general formula (1), they are also included in the compounds represented by the general formula (1).
The compounds represented by I) are not limited to these.
第1表
個々の活性化合物は、その除草活性にそれぞれ欠点を示
す場合が多くあるが、その場合2種の活性化合物を組合
せた場合の除草活性が、その2種の化合物の各々の活性
の単純な合計(期待される活性)よりも大きくなる場合
にこれを相乗作用という。2種の除草剤の特定組合せに
より期待される活性は、次のようにして計算することが
できる。In many cases, the individual active compounds shown in Table 1 exhibit drawbacks in their herbicidal activity, but in such cases, the herbicidal activity of the combination of two active compounds is simply When the total activity is greater than the expected activity, this is called synergism. The expected activity of a particular combination of two herbicides can be calculated as follows.
(Colby S、R,除草剤の組合せの相乗及び拮抗
作用反応の計算rWeedJ 15巻20〜22頁、1
967年を参照)α:除草剤AをaKg/haの量で処
理した時の抑制率
β:除草剤BをbKg/haの量で処理した時の抑制率
E:除草剤AをaKg/ha、除草剤BをbKg/ha
の量で処理した場合に期待される抑制率即ち、実際の抑
制率が上記計算より大きいならば組合せによる活性は相
乗作用を示すということができる。(Colby S, R, Calculation of synergistic and antagonistic responses of herbicide combinations rWeedJ vol. 15, pp. 20-22, 1
967) α: Inhibition rate when herbicide A is treated at a Kg/ha amount β: Suppression rate when herbicide B is treated at bKg/ha amount E: Herbicide A is aKg/ha , herbicide B bKg/ha
If the expected inhibition rate, that is, the actual inhibition rate when treated with the above amount, is greater than the above calculation, it can be said that the combined activity exhibits a synergistic effect.
以下本発明を実施例によりさらに具体的に説明するが、
本発明における化合物、製剤量、剤形等は実施例のみに
限定されるものではない。Hereinafter, the present invention will be explained in more detail with reference to Examples.
The compounds, dosage amounts, dosage forms, etc. in the present invention are not limited to the examples.
尚、「部」は全て重量部を意味する。In addition, all "parts" mean parts by weight.
父金桝上 フロアブル
化合物隘3 5部
グリホセート −・−・・・−・−20部アゲリ
シールB −710−一−−−・−10部(非イオン性
界面活性剤:花王アトラス■商品名)ルノックス100
OC・−−一−−−−・・・ 0.5部(アニオン性界
面活性剤:東邦化学■商品名)1%ロドポール水
・−−−−−−20部(増粘剤:ローン・ブーラン社商
品名)水 −・・・−44
,5部以上を均一に混合し、フロアブル剤にする。Father Kanemasu Flowable Compound Volume 3 5 parts Glyphosate -・-・・・・−20 parts Ageliseal B −710-1 −−・・−10 parts (Nonionic surfactant: Kao Atlas ■Product name) Lunox 100
OC・---1---- 0.5 parts (anionic surfactant: Toho Chemical ■trade name) 1% rhodopol water
・---20 parts (thickener: Lone Boulin product name) Water ----44
, 5 parts or more are mixed uniformly to form a flowable agent.
y金斑主 フロアブル
化合物隘8 −−−−−−−−−−〜0.5部
グリホセート ・−・−・−・・ 25部アゲ
リシールB−710・−・・−9,5部(非イオン性界
面活性剤:花王アトラス■商品名)ルノソクス1000
.C−・・・・−−−−0,5部(アニオン性界面活性
剤:東邦化学■商品名)1%ロドボール水 ・−・
−・−20部(増粘剤:ローン・ブーラン社商品名)水
−一一一一一・44.5
部以上を均一に混合し、フロアブル剤にする。y Gold spot main Flowable compound 8 ----------0.5 parts Glyphosate 25 parts Agelisil B-710--9.5 parts (non-ionic Surfactant: Kao Atlas ■Product name) Lunosox 1000
.. C-・・・・・・・・・0.5 parts (anionic surfactant: Toho Chemical ■trade name) 1% rhodobol water ・-・
-・-20 parts (thickener: Lone Boulin product name) water -11111・44.5
Mix uniformly at least 10 parts to make a flowable agent.
区金匠1 フロアブル
化合物N[L6 1部グリホセー
ト ・−・・−・−25部アゲリシールB−71
0・−・−・ 10部(非イオン性界面活性剤:花王
アトラス■商品名)ルノソクス1000 C−−−−−
〜−・−0,5部(アニオン性界面活性剤:東邦化学■
商品名)1%ロドポール水 −−−−−−・ 2
0部(増粘剤:ローン・ブーラン社商品名)水
・曲−43,5部 ゛以上を均一に混合
し、フロアブル剤にする。Kukinsho 1 Flowable Compound N[L6 1 part Glyphosate ・-・・-・-25 parts Ageliseal B-71
0・-・-・10 parts (Nonionic surfactant: Kao Atlas ■Product name) Lunosox 1000 C------
~-・-0.5 parts (anionic surfactant: Toho Chemical ■
Product name) 1% Rhodopol water ---------・2
0 parts (thickener: Lone Boulin product name) water
・Music - 43.5 parts ゛Mix the above ingredients uniformly to make a flowable agent.
y企桝土 フロアブル
化合物!113 2部グルホシネ
ート −−−−−・−・・−23部アゲリシールB
−710・−・−10部(非イオン性界面活性剤:花王
アトラス■商品名)ルノソクス1000C−・・−−−
−−−−0,5部(アニオン性界面活性剤:東邦化学■
商品名)1%ロドボール水 ・・・−・・・ 2
0部(増粘剤:ローン・ブーラン社商品名)水
−曲−44,5部以上を均一に混合し、フ
ロアブル剤にする。y Kakumasuto Flowable compound! 113 2 parts glufosinate -------・-・・-23 parts Ageliseal B
-710・−・−10 parts (Nonionic surfactant: Kao Atlas ■Product name) Lunosox 1000C−・・−−
---0.5 parts (anionic surfactant: Toho Chemical ■
Product name) 1% rhodobol water ・・・−・・・ 2
0 parts (thickener: Lone Boulin product name) water
-Mix 44, 5 parts or more uniformly to make a flowable agent.
y金車1 フロアブル
化合物隘4 1部
グルホシネート −−−−−・−−−−−18部ア
ゲリシールB −710−−−−−−・ 10部(非
イオン性界面活性剤:花王アトラス■商品名)ルノソク
スtoooc・・−−−−−−−−−0,5部(アニオ
ン性界面活性剤:東邦化学■商品名)1%ロドボール水
−・−20部
(増粘剤:ローン・ブーラン社商品名)水
−・−−−〜・・50.5部以上を均
一に混合し、フロアブル剤にする。y Metal wheel 1 Flowable compound 4 1 part Glufosinate -------18 parts Agelisil B -710--10 parts (Nonionic surfactant: Kao Atlas ■Product name ) Runosox toooc...---0.5 parts (Anionic surfactant: Toho Chemical ■Product name) 1% Rhodobol water ---20 parts (Thickener: Lone Boulin product) noun) water
-・---~・Mix 50.5 parts or more uniformly to make a flowable agent.
配合例6 フロアブル
化合物魔8 2部
グルホシネート −−−−−−−−・−23部アゲ
リシールB−710・−・−10部(非イオン性界面活
性剤:花王アトラス(411商品名)ルノックス100
0 C−・−・・・−・−・ 0.5部(アニオン性界
面活性剤:東邦化学(株間品名)1%ロドボール水
−・・−20部(増粘剤:ローン・ブーラン社商品名
)水 ・−−−−−−44、
5部以上を均一に混合し、フロアブル剤にする。Formulation Example 6 Flowable Compound Demon 8 2 parts Glufosinate ---23 parts Agelisil B-710 ---10 parts (Nonionic surfactant: Kao Atlas (411 brand name) Lunox 100
0 C-・-・・・・・0.5 part (anionic surfactant: Toho Chemical (product name: Co., Ltd.) 1% Rhodobol water
−・・−20 parts (thickener: Lone Boulin product name) Water ・−−−−−44,
Mix 5 parts or more evenly to make a flowable agent.
区企皿エ フロアブル
化合物11h1 1部ビアラフオ
ス −・・・・・・・・−35部アゲリシールB
−710−・・−5部、(非イオン性界面活性剤:花
王アトラス■商品名)ルノックス1000 C−−−−
−−・−・−・ 0.5部(アニオン性界面活性剤:東
邦化学側商品名)1%ロドポール水 −・・・・−
14部(増粘剤:ローン・ブーラン社商品名)水
−−−−−−−44、5部以上
を均一に混合し、フロアブル剤にする。Kukitarae Flowable Compound 11h1 1 part Bialafosu - 35 parts Ageli Seal B
-710-...-5 parts, (Nonionic surfactant: Kao Atlas ■Product name) Lunox 1000 C----
−−・−・−・0.5 part (anionic surfactant: Toho Chemical brand name) 1% Rhodopol water −・−・−
14 parts (thickener: Lone Boulin product name) water
----------- 44. Mix 5 parts or more uniformly to make a flowable agent.
侃企拠主 フロアブル
化合物魚7 5部
ビアラフオス −−−−−・・−25部アゲリシ
ールB−710−・−・ 5部(非イオン性界面活
性剤:花王アトラス■商品名)ルノックス100OC・
−・−・・−−−−−0,5部(アニオン性界面活性剤
:東邦化学■商品名)1%ロドボール水 −・−・
20部(増粘剤:ローン・ブーラン社商品名)水
−・・・−・44.5部以上
を均一に混合し、フロアブル剤にする。Sponsor: Flowable Compound Fish 7 5 parts Bealaf Male -------25 parts Ageliseal B-710--5 parts (Non-ionic surfactant: Kao Atlas ■Product name) Lunox 100OC・
−・−・・−−−−−0.5 parts (anionic surfactant: Toho Chemical ■trade name) 1% Rhodobol water −・−・
20 parts (thickener: Lone Boulin product name) water
---44.5 parts or more are mixed uniformly to make a flowable agent.
拭肱五 茎葉処理による除草効果試験箱15cm、横
22cm、深さ6cmのプラスチック製箱に殺菌した洪
積土壌を入れ、ノビエ、メヒシバ、エノコログサ、イヌ
タデ、イヌビニ及びアサガオの種子をそれぞれスポット
状に播種し約1.5cm覆土した。各植物が2〜3葉期
に達した時、有効成分量が所定の薬量になるように茎葉
部に均一に散布した。散布の際の薬液は、前記配合例の
フロアブル剤を水で希釈して小型スプレーで各種雑草の
茎葉部の全面に散布した。薬液散布4週間後に各種雑草
に対する除草効果を次の判定基準に従い調査した。下記
の判定基準に従っそ調査した。結果は第2表及び第3表
に示す。Test box for herbicidal effect by foliage treatment Put sterilized diluvial soil in a plastic box measuring 15 cm wide, 22 cm wide, and 6 cm deep, and sow seeds of wild grass, Japanese knotweed, foxtail grass, Japanese knotweed, Japanese knotweed, and morning glory in spots. The soil was covered with approximately 1.5 cm of soil. When each plant reached the 2-3 leaf stage, the active ingredient was uniformly sprayed on the stems and leaves so that the amount of the active ingredient was a predetermined amount. The chemical solution used for spraying was the flowable agent of the formulation example described above diluted with water and sprayed over the entire surface of the stems and leaves of various weeds using a small sprayer. Four weeks after spraying the chemical solution, the herbicidal effect on various weeds was investigated according to the following criteria. The investigation was conducted according to the following criteria. The results are shown in Tables 2 and 3.
判定基準 殺草率
0 0〜9%
但し、上記の殺草率は、薬剤処理区の地上部生草重およ
び無処理区の地上部生草重を測定して下記の式により求
めたものである。Judgment Criteria Weed killing rate 0 0-9% However, the above weed killing rate was determined by the following formula by measuring the weight of above-ground plants in the chemically treated area and the weight of above-ground plants in the untreated area.
無処理区のtt!!上笥S王早里
第2表
第2表−続き
以下余白
表中、計算値は前記Co1byの式より求めた期待値を
示す。tt in untreated area! ! Table 2, Table 2, Table 2 - Continued In the blank table below, the calculated values indicate the expected values obtained from the Colby equation.
以上の表から明らかなように、本発明組成物は、一般式
(1)で表される化合物及び従来公知の除草剤それぞれ
の活性の単純な合計にとどまらず、より大きな相乗的除
草活性を有しており更にかつ低薬量で対象雑草を完全に
防除することができる。As is clear from the above table, the composition of the present invention has greater synergistic herbicidal activity than the simple sum of the activities of the compound represented by general formula (1) and the conventionally known herbicides. Furthermore, target weeds can be completely controlled with a low dose.
Claims (1)
低級アルキル基を示す。Rは低級アルキル基を示す。X
およびYはそれぞれ独立して、低級アルキル基または低
級アルコキシ基を示す。〕 で表されるピラゾールスルホニルウレア誘導体とN−ホ
スホノメチルグリシン、アンモニウム−(3−アミノカ
ルボキシプロピル)−メチルホスフィネートまたは(2
−アミノ−4−メチルホスフィノブチリル)アラニルア
ラニンのうちの一種を有効成分として含有することを特
徴とする除草剤組成物。[Claims] General formula (I): ▲There are numerical formulas, chemical formulas, tables, etc.▼(I) [In the formula, A represents a lower alkyl group. B represents a hydrogen atom or a lower alkyl group. R represents a lower alkyl group. X
and Y each independently represent a lower alkyl group or a lower alkoxy group. ] Pyrazolesulfonylurea derivative represented by N-phosphonomethylglycine, ammonium-(3-aminocarboxypropyl)-methylphosphinate or (2
-A herbicidal composition characterized by containing one kind of alanylalanine (amino-4-methylphosphinobutyryl) as an active ingredient.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6045485A JPS61218503A (en) | 1985-03-25 | 1985-03-25 | Herbicidal composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6045485A JPS61218503A (en) | 1985-03-25 | 1985-03-25 | Herbicidal composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61218503A true JPS61218503A (en) | 1986-09-29 |
JPH0462286B2 JPH0462286B2 (en) | 1992-10-05 |
Family
ID=13142728
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6045485A Granted JPS61218503A (en) | 1985-03-25 | 1985-03-25 | Herbicidal composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61218503A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0252237A2 (en) * | 1986-05-09 | 1988-01-13 | Hoechst Aktiengesellschaft | Herbicidal agents |
JP2002522457A (en) * | 1998-08-13 | 2002-07-23 | アベンティス・クロップサイエンス・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | Herbicide composition for resistant or resistant rice crops |
-
1985
- 1985-03-25 JP JP6045485A patent/JPS61218503A/en active Granted
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0252237A2 (en) * | 1986-05-09 | 1988-01-13 | Hoechst Aktiengesellschaft | Herbicidal agents |
JP2002522457A (en) * | 1998-08-13 | 2002-07-23 | アベンティス・クロップサイエンス・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | Herbicide composition for resistant or resistant rice crops |
US20140121107A1 (en) * | 1998-08-13 | 2014-05-01 | Bayer Intellectual Property Gmbh | Herbicidal compositions for tolerant or resistant rice crops |
Also Published As
Publication number | Publication date |
---|---|
JPH0462286B2 (en) | 1992-10-05 |
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