JPH06227918A - Herbicidal composition - Google Patents
Herbicidal compositionInfo
- Publication number
- JPH06227918A JPH06227918A JP1648993A JP1648993A JPH06227918A JP H06227918 A JPH06227918 A JP H06227918A JP 1648993 A JP1648993 A JP 1648993A JP 1648993 A JP1648993 A JP 1648993A JP H06227918 A JPH06227918 A JP H06227918A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- group
- glyphosate
- herbicidal
- herbicidal composition
- 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.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 24
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 23
- 150000001875 compounds Chemical class 0.000 claims abstract description 15
- OEYOMNZEMCPTKN-UHFFFAOYSA-N Butamifos Chemical compound CCC(C)NP(=S)(OCC)OC1=CC(C)=CC=C1[N+]([O-])=O OEYOMNZEMCPTKN-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000005562 Glyphosate Substances 0.000 claims abstract description 9
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 9
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229940097068 glyphosate Drugs 0.000 claims abstract description 9
- 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 claims abstract description 8
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 5
- 125000005843 halogen group Chemical group 0.000 claims abstract description 4
- -1 setoxidim Chemical compound 0.000 claims description 9
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- 125000004429 atom Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 241000196324 Embryophyta Species 0.000 abstract description 14
- 239000002689 soil Substances 0.000 abstract description 8
- XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 abstract description 6
- HQQTZCPKNZVLFF-UHFFFAOYSA-N 4h-1,2-benzoxazin-3-one Chemical class C1=CC=C2ONC(=O)CC2=C1 HQQTZCPKNZVLFF-UHFFFAOYSA-N 0.000 abstract description 4
- CSPPKDPQLUUTND-NBVRZTHBSA-N Sethoxydim Chemical compound CCO\N=C(/CCC)C1=C(O)CC(CC(C)SCC)CC1=O CSPPKDPQLUUTND-NBVRZTHBSA-N 0.000 abstract 2
- QHTQREMOGMZHJV-UHFFFAOYSA-N Thiobencarb Chemical compound CCN(CC)C(=O)SCC1=CC=C(Cl)C=C1 QHTQREMOGMZHJV-UHFFFAOYSA-N 0.000 abstract 1
- MGLWZSOBALDPEK-UHFFFAOYSA-N simetryn Chemical compound CCNC1=NC(NCC)=NC(SC)=N1 MGLWZSOBALDPEK-UHFFFAOYSA-N 0.000 abstract 1
- 230000000694 effects Effects 0.000 description 14
- 239000004009 herbicide Substances 0.000 description 11
- 239000003795 chemical substances by application Substances 0.000 description 10
- 238000009472 formulation Methods 0.000 description 9
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 239000003814 drug Substances 0.000 description 4
- 229940079593 drug Drugs 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000004563 wettable powder Substances 0.000 description 4
- 241000209510 Liliopsida Species 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 241000258957 Asteroidea Species 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 235000001602 Digitaria X umfolozi Nutrition 0.000 description 2
- 240000003176 Digitaria ciliaris Species 0.000 description 2
- 235000017898 Digitaria ciliaris Nutrition 0.000 description 2
- 235000005476 Digitaria cruciata Nutrition 0.000 description 2
- 235000006830 Digitaria didactyla Nutrition 0.000 description 2
- 235000005804 Digitaria eriantha ssp. eriantha Nutrition 0.000 description 2
- 235000010823 Digitaria sanguinalis Nutrition 0.000 description 2
- 244000058871 Echinochloa crus-galli Species 0.000 description 2
- 235000014716 Eleusine indica Nutrition 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 239000012752 auxiliary agent Substances 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- 150000005130 benzoxazines Chemical class 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- 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 description 1
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000005561 Glufosinate Substances 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 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 description 1
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 229920006184 cellulose methylcellulose Polymers 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 229940125782 compound 2 Drugs 0.000 description 1
- FWFSEYBSWVRWGL-UHFFFAOYSA-N cyclohex-2-enone Chemical compound O=C1CCCC=C1 FWFSEYBSWVRWGL-UHFFFAOYSA-N 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004742 propyloxycarbonyl group Chemical group 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000009333 weeding Methods 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は除草組成物に関するもの
である。FIELD OF THE INVENTION The present invention relates to a herbicidal composition.
【0002】[0002]
【従来の技術】現在、農耕地あるいは非農耕地の除草に
は、その目的、用途に応じ多くの種類の除草剤が使用さ
れている。しかし、防除の対象となる雑草の種類は極め
て多く、一方においてはより選択性の高い除草剤の開発
が求められているが、他方においては、より幅広い殺草
スペクトルを有し且つより強力な殺草効果を持つ除草剤
の開発も求められている。2. Description of the Related Art At present, many kinds of herbicides are used for weeding of agricultural land or non-agricultural land depending on the purpose and use. However, the types of weeds to be controlled are extremely large, and on the one hand, the development of more selective herbicides is required, while on the other hand, they have a broader herbicidal spectrum and a stronger herbicidal activity. There is also a demand for the development of herbicides having herbal effects.
【0003】かかる状況に鑑み本発明者らは、これまで
に選択性に優れ且つ殺草活性の高い化合物として新規ベ
ンゾオキサジン系化合物を提案してきた(EPC特許公
開番号第0479420A2号又は特開平5−4977
号公報参照)。一方、グリフォサート(A)、ブタミフ
ォス(B)、セトキシジム(C)、トリフルラリン
(D)、アラクロール(E)、ベンチオカーブ(F)及
びシンメスリン(G)は、公知の除草剤で、それぞれ下
記式In view of such circumstances, the present inventors have proposed a novel benzoxazine compound as a compound having excellent selectivity and high herbicidal activity (EPC Patent Publication No. 0479420A2 or Japanese Patent Laid-Open No. 5-279420). 4977
(See Japanese Patent Publication). On the other hand, glyphosate (A), butamiphos (B), setoxydim (C), trifluralin (D), alachlor (E), benchocarb (F) and synmethrin (G) are known herbicides, each of which has the following formula:
【0004】[0004]
【化2】 [Chemical 2]
【0005】で表される化学構造を有する化合物であ
る。グリフォサート(A)は、広葉雑草に対してやや活
性が低く、また、遅効性で効果の発現の遅い薬剤であ
る。セトキシジム(C)は、シクロヘキセノン系除草剤
で、茎葉処理剤として単子葉雑草に対してのみ選択的効
果を示す。また、トリフルラリン(D)、アラクロール
(E)、ベンチオカーブ(F)およびブタミフォス
(B)は、土壌処理剤として卓効を示すが、広葉雑草に
対してやや活性が弱く、シンメスリン(G)は単子葉雑
草に対して高い活性を示すが、広葉雑草に対して殆ど効
果を示さない。It is a compound having a chemical structure represented by: Glyphosate (A) is a drug having a slightly low activity against broad-leaved weeds, and having a slow-acting effect and a slow onset of effect. Cetoxydim (C) is a cyclohexenone herbicide and shows a selective effect only on monocotyledon weeds as a foliar treatment agent. Also, trifluralin (D), alachlor (E), benchocarb (F) and butamifos (B) are effective as soil treatment agents, but they are slightly less active against broadleaf weeds, and simmethrin (G) is a simple substance. High activity against cotyledon weeds, but little effect against broadleaf weeds.
【0006】[0006]
【発明が解決しようとする課題】前記ベンゾオキサジン
系化合物は、茎葉処理又は土壌処理により広葉雑草並び
に単子葉雑草の両雑草に対して強い殺草活性を示す化合
物であるが、単子葉雑草に対してはやや効果が弱く、十
分な効果を得るためには比較的高い薬量を必要とする。
従って、本発明は、前記ベンゾオキサジン系化合物の広
葉雑草に対する高い除草活性と速い活性の発現という特
性を生かし、更に単子葉雑草にも有効な除草剤を開発す
ることを目的とする。The benzoxazine compound is a compound showing a strong herbicidal activity against both broadleaf weeds and monocotyledonous weeds by foliar treatment or soil treatment. The effect is rather weak, and a relatively high dose is required to obtain a sufficient effect.
Therefore, it is an object of the present invention to develop a herbicide that is effective against monocotyledon weeds, making the best use of the characteristics of the above-mentioned benzoxazine compounds to exhibit high herbicidal activity against broadleaf weeds and rapid activity.
【0007】[0007]
【課題を解決するための手段】本発明者らは、上記課題
を解決すべく鋭意研究した結果、前記ベンゾオキサジン
系化合物のうちの特定の化合物と、公知の除草剤である
グリフォサート、ブタミフォス、セトキシジム、トリフ
ルラリン、アラクロール、ベンチオカーブ及びシンメス
リンの群から選ばれた少なくとも1種の化合物を混合す
ることにより、単子葉雑草に対しても速効性で、且つ優
れた除草効果を持つ組成物を得ることに成功し、本発明
を完成した。Means for Solving the Problems As a result of intensive studies to solve the above problems, the present inventors have found that a specific compound among the above-mentioned benzoxazine compounds and glyphosate, butamifos, and setoxydim which are known herbicides. , Trifluralin, alachlor, benchocarb and at least one compound selected from the group of synmethrin are mixed to obtain a composition having a fast-acting effect on monocotyledon weeds and an excellent herbicidal effect. Succeeded and completed the present invention.
【0008】即ち本発明に従えば、(i)一般式
(I):That is, according to the present invention, (i) the general formula (I):
【0009】[0009]
【化3】 [Chemical 3]
【0010】〔式中、R1 及びR2 はそれぞれ独立に低
級アルキル基を、R3 及びR4 はそれぞれ独立に水素原
子または置換されてもよい低級アルキル基(ここで、置
換基としてはハロゲン原子、低級アルコキシ基または低
級アルコキシカルボニル基のいずれかである)を示す〕
で表されるベンゾオキサジン−3−オン誘導体と、(i
i)グリフォサート、ブタミフォス、セトキシジム、ト
リフルラリン、アラクロール、ベンチオカーブ及びシン
メスリンの群から選ばれた少なくとも1種の化合物とを
有効成分として含有する除草組成物が提供される。[In the formula, R 1 and R 2 are each independently a lower alkyl group, and R 3 and R 4 are each independently a hydrogen atom or an optionally substituted lower alkyl group (wherein the substituent is halogen. Atom, a lower alkoxy group or a lower alkoxycarbonyl group)]
A benzoxazin-3-one derivative represented by
There is provided a herbicidal composition containing, as an active ingredient, i) at least one compound selected from the group consisting of glyphosate, butamiphos, setoxydim, trifluralin, alachlor, benchocarb and synmethrin.
【0011】前記一般式(I)において、R1 、R2 、
R3 及びR4 で示される低級アルキル基としては、直鎖
及び分枝鎖の炭素数1〜6、好ましくは1〜4のアルキ
ル基、例えばメチル基、エチル基、プロピル基、イソプ
ロピル基、ブチル基、イソブチル基等が挙げられる。ま
た、R3 及びR4 で示される置換低級アルキル基におい
て、置換されうる置換基としては、ハロゲン原子として
フッ素原子、塩素原子または臭素原子の1〜3個を、低
級アルコキシ基としてメトキシ基、エトキシ基、プロポ
キシ基またはブトキシ基等の炭素数1〜4の低級アルコ
キシ基を、低級アルコキシカルボニル基としてメトキシ
カルボニル基、エトキシカルボニル基またはプロポキシ
カルボニル基等のアルコキシ部分の炭素数が1〜6、好
ましくは1〜4の低級アルコキシカルボニル基を挙げる
ことができる。In the above general formula (I), R 1 , R 2 ,
The lower alkyl group represented by R 3 and R 4 is a linear or branched alkyl group having 1 to 6 carbon atoms, preferably 1 to 4 carbon atoms, for example, methyl group, ethyl group, propyl group, isopropyl group, butyl group. Group, isobutyl group and the like. Further, in the substituted lower alkyl group represented by R 3 and R 4 , the substituent that may be substituted is 1 to 3 of a fluorine atom, a chlorine atom or a bromine atom as a halogen atom, a methoxy group or an ethoxy group as a lower alkoxy group. Group, a lower alkoxy group having 1 to 4 carbon atoms such as a propoxy group or a butoxy group, a lower alkoxycarbonyl group such as a methoxycarbonyl group, an ethoxycarbonyl group or a propoxycarbonyl group having 1 to 6 carbon atoms, preferably There may be mentioned 1 to 4 lower alkoxycarbonyl groups.
【0012】一般式(I)のベンゾオキサジン−3−オ
ン誘導体は、前述のEPC特許公開番号第047942
0A2号公報又は特開平5−4977号公報記載の方法
に従い製造することができる。製造した化合物の代表例
を第1表に示す。The benzoxazin-3-one derivatives of the general formula (I) are described in the above-mentioned EPC Patent Publication No. 047942.
It can be produced according to the method described in JP-A-0A2 or JP-A-5-4977. Table 1 shows typical examples of the produced compounds.
【0013】[0013]
【表1】 [Table 1]
【0014】公知の除草剤であるグリフォサート
(A)、ブタミフォス(B)、セトキシジム(C)、ト
リフルラリン(D)、アラクロール(E)、ベンチオカ
ーブ(F)及びシンメスリン(G)は、市販されている
薬剤で、容易に入手することのできる。また、グリフォ
サート及びブタミフォスは、有機リン系の代表的除草剤
であり、他の同様の特性を有する有機リン系除草剤、例
えばグルフォシネートやビアラフォス等との代替の可能
性が示唆される。The known herbicides glyphosate (A), butamiphos (B), setoxydim (C), trifluralin (D), alachlor (E), benchocarb (F) and synmethrin (G) are commercially available. It is a drug and can be easily obtained. Further, glyphosate and butamifos are typical organophosphorus herbicides, and it is suggested that they may be substituted with other organophosphorus herbicides having similar properties, such as glufosinate and bialaphos.
【0015】本発明に係る除草組成物は、広葉雑草並び
に単子葉雑草の両雑草に対し、土壌処理或いは茎葉処理
により優れた除草効果の得られるものである。本発明の
組成物は、上記組成物をそのまま使用しても良いが、各
種の担体、界面活性剤、その他の製剤用補助剤を配合し
て、粉剤、粒剤、フロアブル剤、水和剤、乳剤、油剤等
に製剤化して施用するのが好ましい。ここで担体として
は、固体又は液体のいずれでもよく、例えば、タルク、
クレー、ベントナイト、カオリン、珪藻土、炭酸カルシ
ウム、木炭、澱粉、アラビアゴム、水、アルコール、ケ
ロシン、ナフサ、キシレン、シクロヘキサン、アセト
ン、ジメチルホルムアミド等を挙げることができる。界
面活性剤としては、例えば、アルキル硫酸、アルキルア
リールスルホン酸塩、ジアルキルスルホサクシネート塩
等を、その他の製剤用補助剤としては、例えば、アルギ
ン酸塩、ポリビニールアルコール、CMC等が挙げられ
る。The herbicidal composition according to the present invention has an excellent herbicidal effect on both broadleaf weeds and monocotyledonous weeds by soil treatment or foliage treatment. The composition of the present invention may be used as it is, but various carriers, surfactants, other formulation auxiliary agents are mixed, and powders, granules, flowable agents, wettable powders, It is preferable to formulate and apply it in an emulsion, an oil agent or the like. Here, the carrier may be either solid or liquid, for example, talc,
Clay, bentonite, kaolin, diatomaceous earth, calcium carbonate, charcoal, starch, gum arabic, water, alcohol, kerosene, naphtha, xylene, cyclohexane, acetone, dimethylformamide and the like can be mentioned. Examples of the surfactant include alkylsulfuric acid, alkylarylsulfonate, dialkylsulfosuccinate salt and the like, and examples of other formulation auxiliary agents include alginate, polyvinyl alcohol, CMC and the like.
【0016】本発明に係る除草組成物は、乳剤、水和
剤、粉剤、粒剤などの剤型にて供することができ、必要
に応じて多種の除草剤、各種殺虫剤、殺菌剤、植物成長
調節剤などに混合施用してもよい。The herbicidal composition according to the present invention can be provided in the form of emulsions, wettable powders, powders, granules and the like, and if necessary, various herbicides, various insecticides, fungicides, plants. You may mix and apply it to a growth regulator.
【0017】本発明の実施にあたり、本発明の除草組成
物中の前記成分(i)及び(ii)の濃度は広範囲にわた
り変えることができるが、一般には10アールあたり成
分(i)1〜50g及び成分(ii)5〜100gの範囲
で使用するのが好ましい。前記各種製剤を製造するに際
しては、有効成分を5〜70%の範囲で含有するように
製造することができる。In carrying out the present invention, the concentrations of the above-mentioned components (i) and (ii) in the herbicidal composition of the present invention can be varied over a wide range, but generally 1 to 50 g of the component (i) per 10 are and It is preferable to use the component (ii) in the range of 5 to 100 g. When manufacturing the above-mentioned various preparations, it may be manufactured so as to contain the active ingredient in the range of 5 to 70%.
【0018】[0018]
【実施例】以下、本発明を製剤例及び試験例をもって更
に詳しく説明するが、本発明の範囲をこれら製剤例及び
試験例に限定するものでないことはいうまでもない。例
中の%は重量%である。EXAMPLES The present invention will be described in more detail below with reference to formulation examples and test examples, but it goes without saying that the scope of the present invention is not limited to these formulation examples and test examples. In the examples,% is% by weight.
【0019】製剤例1(水和剤) 化合物番号7の化合物5%、セトキシジム(C)30
%、アルキルベンゼンスルホン酸ソーダ2%、ポリオキ
シエチレンアルキルアリールエーテル3%及びジークラ
イト60%を均一に混合粉砕して水和剤とした。 Formulation Example 1 (wettable powder ) Compound No. 7 5%, setoxydim (C) 30
%, Sodium alkylbenzene sulfonate 2%, polyoxyethylene alkylaryl ether 3%, and Sikelite 60% were uniformly mixed and pulverized to obtain a wettable powder.
【0020】製剤例2(乳剤) 化合物番号3の化合物5%、ブタミホス(B)25%、
ポリオキシエチレンアルキルエーテル20%及びキシレ
ン50%を均一に混合して乳剤とした。 Formulation Example 2 (emulsion ) Compound No. 3 5%, butamiphos (B) 25%,
20% polyoxyethylene alkyl ether and 50% xylene were uniformly mixed to obtain an emulsion.
【0021】製剤例3(粒剤) 化合物番号3の化合物2%、シンメスリン(G)3%、
ベントナイト20%、ドデシルベンゼンスルホン酸ソー
ダ2%及びクレー73%を均一に混和し、水約20%を
加えて練混した。これを造粒機で造粒、乾燥して粒剤と
した。 Formulation Example 3 (granules ) Compound No. 3 compound 2%, Synmethrin (G) 3%,
Bentonite 20%, sodium dodecylbenzenesulfonate 2% and clay 73% were uniformly mixed, and about 20% of water was added and kneaded. This was granulated with a granulator and dried to obtain a granule.
【0022】次に、本発明組成物の効果を試験例により
具体的に示す。試験例1(茎葉処理 ) 土壌を充填した6cm×15cm×10cmのシードリ
ングケースにメヒシバ、イヌビエ、イヌタデの各種子を
播種した。室温で10日間育成した後、製剤例1に準じ
て水和剤とした試験化合物(単剤又は混合剤)の所定量
を、10アール当たり200リットル相当の水で希釈
し、茎葉部全面に均一に散布した。薬剤処理3週間後に
効果を肉眼で観察、殺草程度(5:完全枯死〜0:無作
用)で評価した。得られた結果を第2表に示す。Next, the effects of the composition of the present invention will be specifically shown by test examples. Test Example 1 (Stem and Leaf Treatment ) Various seeds of crabgrass, barnyard grass, and starfish were sown in a 6 cm × 15 cm × 10 cm seedling case filled with soil. After growing at room temperature for 10 days, a predetermined amount of the test compound (single agent or mixed agent) which was made into a wettable powder according to Formulation Example 1 was diluted with 200 liters of water equivalent to 10 ares, and was uniformly applied to the entire surface of the foliage. Sprinkled on. After 3 weeks from the drug treatment, the effect was visually observed and evaluated by the degree of herbicidal activity (5: complete death to 0: no action). The results obtained are shown in Table 2.
【0023】[0023]
【表2】 [Table 2]
【0024】試験例2(土壌処理) 土壌を充填した6cm×15cm×10cmのシードリ
ングケースにメヒシバ、イヌビエ、イヌタデの各種子を
播種した。播種翌日に、製剤例1に準じて水和剤とした
試験化合物(単剤又は混合剤)の所定量を、10アール
当たり200リットル相当の水で希釈し、土壌表面に均
一に散布した。薬剤処理2週間後に効果を肉眼で観察、
殺草程度(5:完全枯死〜0:無作用)で評価した。得
られた結果を第3表に示す。 Test Example 2 (Soil Treatment ) Various seeds of the crabgrass, the barnyard grass, and the starfish were sown in a 6 cm × 15 cm × 10 cm seed ring case filled with soil. On the day after seeding, a prescribed amount of the test compound (single agent or mixed agent) which was made into a wettable powder according to Formulation Example 1 was diluted with 200 liters of water equivalent to 10 ares and sprayed uniformly on the soil surface. 2 weeks after the drug treatment, the effect is visually observed,
The degree of grass killing (5: complete death to 0: no action) was evaluated. The results obtained are shown in Table 3.
【0025】[0025]
【表3】 [Table 3]
【0026】[0026]
【発明の効果】以上のとおり本発明の除草組成物は、両
薬剤の相乗効果により、単剤では防除困難な広範囲の雑
草に対して、低薬量で優れた除草効果の得られるもので
ある。INDUSTRIAL APPLICABILITY As described above, the herbicidal composition of the present invention has a synergistic effect of both agents and is capable of obtaining an excellent herbicidal effect with a low dose against a wide range of weeds which are difficult to control by a single agent. .
───────────────────────────────────────────────────── フロントページの続き (72)発明者 佐合 隆一 神奈川県伊勢原市下粕屋1787−1 (72)発明者 井貝 敬太郎 神奈川県平塚市田村6348 ─────────────────────────────────────────────────── ─── Continued Front Page (72) Inventor Ryuichi Saai 1787-1 Shimokasuya, Isehara City, Kanagawa Prefecture (72) Inventor Keitaro Ikai 6348 Tamura, Hiratsuka City, Kanagawa Prefecture
Claims (1)
を、R3 及びR4 はそれぞれ独立に水素原子または置換
されてもよい低級アルキル基(ここで、置換基としては
ハロゲン原子、低級アルコキシ基または低級アルコキシ
カルボニル基のいずれかである)を示す〕で表されるベ
ンゾオキサジン−3−オン誘導体と、(ii)グリフォサ
ート、ブタミフォス、セトキシジム、トリフルラリン、
アラクロール、ベンチオカーブ及びシンメリスンの群か
ら選ばれた少なくとも1種の化合物とを有効成分として
含有する除草組成物。1. (i) General formula (I): [In the formula, R 1 and R 2 each independently represent a lower alkyl group, and R 3 and R 4 each independently represent a hydrogen atom or an optionally substituted lower alkyl group (wherein the substituent is a halogen atom, a lower atom). An alkoxy group or a lower alkoxycarbonyl group)], and (ii) glyphosate, butamiphos, setoxidim, trifluralin,
A herbicidal composition containing, as an active ingredient, at least one compound selected from the group consisting of Alacrole, Bentocarb and Symmelisin.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1648993A JPH06227918A (en) | 1993-02-03 | 1993-02-03 | Herbicidal composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1648993A JPH06227918A (en) | 1993-02-03 | 1993-02-03 | Herbicidal composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH06227918A true JPH06227918A (en) | 1994-08-16 |
Family
ID=11917708
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1648993A Pending JPH06227918A (en) | 1993-02-03 | 1993-02-03 | Herbicidal composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH06227918A (en) |
-
1993
- 1993-02-03 JP JP1648993A patent/JPH06227918A/en active Pending
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