JPH09255508A - Herbicidal composition - Google Patents
Herbicidal compositionInfo
- Publication number
- JPH09255508A JPH09255508A JP6452096A JP6452096A JPH09255508A JP H09255508 A JPH09255508 A JP H09255508A JP 6452096 A JP6452096 A JP 6452096A JP 6452096 A JP6452096 A JP 6452096A JP H09255508 A JPH09255508 A JP H09255508A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- generic name
- formula
- herbicidal
- compounds
- 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
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 31
- 239000000203 mixture Substances 0.000 title claims abstract description 27
- 150000001875 compounds Chemical class 0.000 claims abstract description 47
- 239000004480 active ingredient Substances 0.000 claims abstract description 7
- 239000004009 herbicide Substances 0.000 abstract description 20
- 239000000126 substance Substances 0.000 abstract description 7
- BGNQYGRXEXDAIQ-UHFFFAOYSA-N Pyrazosulfuron-ethyl Chemical group C1=NN(C)C(S(=O)(=O)NC(=O)NC=2N=C(OC)C=C(OC)N=2)=C1C(=O)OCC BGNQYGRXEXDAIQ-UHFFFAOYSA-N 0.000 abstract description 2
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 2
- 241000192043 Echinochloa Species 0.000 abstract 1
- 230000002349 favourable effect Effects 0.000 abstract 1
- 230000000694 effects Effects 0.000 description 11
- 241000209094 Oryza Species 0.000 description 9
- 235000007164 Oryza sativa Nutrition 0.000 description 9
- 230000005764 inhibitory process Effects 0.000 description 9
- 235000009566 rice Nutrition 0.000 description 9
- 230000002195 synergetic effect Effects 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000008187 granular material Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000004563 wettable powder Substances 0.000 description 6
- 241000196324 Embryophyta Species 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000003945 anionic surfactant Substances 0.000 description 3
- 230000009969 flowable effect Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000005472 Bensulfuron methyl Substances 0.000 description 2
- RRNIZKPFKNDSRS-UHFFFAOYSA-N Bensulide Chemical compound CC(C)OP(=S)(OC(C)C)SCCNS(=O)(=O)C1=CC=CC=C1 RRNIZKPFKNDSRS-UHFFFAOYSA-N 0.000 description 2
- OEYOMNZEMCPTKN-UHFFFAOYSA-N Butamifos Chemical compound CCC(C)NP(=S)(OCC)OC1=CC(C)=CC=C1[N+]([O-])=O OEYOMNZEMCPTKN-UHFFFAOYSA-N 0.000 description 2
- IKYICRRUVNIHPP-UHFFFAOYSA-N Dimethametryn Chemical compound CCNC1=NC(NC(C)C(C)C)=NC(SC)=N1 IKYICRRUVNIHPP-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- XMQFTWRPUQYINF-UHFFFAOYSA-N bensulfuron-methyl Chemical group COC(=O)C1=CC=CC=C1CS(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 XMQFTWRPUQYINF-UHFFFAOYSA-N 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
- WZDDLAZXUYIVMU-UHFFFAOYSA-N bromobutide Chemical compound CC(C)(C)C(Br)C(=O)NC(C)(C)C1=CC=CC=C1 WZDDLAZXUYIVMU-UHFFFAOYSA-N 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 230000001276 controlling effect Effects 0.000 description 2
- 239000002552 dosage form Substances 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- DEDOPGXGGQYYMW-UHFFFAOYSA-N molinate Chemical compound CCSC(=O)N1CCCCCC1 DEDOPGXGGQYYMW-UHFFFAOYSA-N 0.000 description 2
- 239000005648 plant growth regulator Substances 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- BDQWWOHKFDSADC-UHFFFAOYSA-N 2-(2,4-dichloro-3-methylphenoxy)-n-phenylpropanamide Chemical compound C=1C=CC=CC=1NC(=O)C(C)OC1=CC=C(Cl)C(C)=C1Cl BDQWWOHKFDSADC-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 239000005484 Bifenox Substances 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- VYNOULHXXDFBLU-UHFFFAOYSA-N Cumyluron Chemical compound C=1C=CC=CC=1C(C)(C)NC(=O)NCC1=CC=CC=C1Cl VYNOULHXXDFBLU-UHFFFAOYSA-N 0.000 description 1
- 239000005502 Cyhalofop-butyl Substances 0.000 description 1
- TYIYMOAHACZAMQ-CQSZACIVSA-N Cyhalofop-butyl Chemical group C1=CC(O[C@H](C)C(=O)OCCCC)=CC=C1OC1=CC=C(C#N)C=C1F TYIYMOAHACZAMQ-CQSZACIVSA-N 0.000 description 1
- YUBJPYNSGLJZPQ-UHFFFAOYSA-N Dithiopyr Chemical compound CSC(=O)C1=C(C(F)F)N=C(C(F)(F)F)C(C(=O)SC)=C1CC(C)C YUBJPYNSGLJZPQ-UHFFFAOYSA-N 0.000 description 1
- BXEHUCNTIZGSOJ-UHFFFAOYSA-N Esprocarb Chemical compound CC(C)C(C)N(CC)C(=O)SCC1=CC=CC=C1 BXEHUCNTIZGSOJ-UHFFFAOYSA-N 0.000 description 1
- 239000005567 Imazosulfuron Substances 0.000 description 1
- NAGRVUXEKKZNHT-UHFFFAOYSA-N Imazosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N3C=CC=CC3=NC=2Cl)=N1 NAGRVUXEKKZNHT-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 244000207740 Lemna minor Species 0.000 description 1
- 235000006439 Lemna minor Nutrition 0.000 description 1
- SUSRORUBZHMPCO-UHFFFAOYSA-N MC-4379 Chemical compound C1=C([N+]([O-])=O)C(C(=O)OC)=CC(OC=2C(=CC(Cl)=CC=2)Cl)=C1 SUSRORUBZHMPCO-UHFFFAOYSA-N 0.000 description 1
- 239000005574 MCPA Substances 0.000 description 1
- LVKTWOXHRYGDMM-UHFFFAOYSA-N Naproanilide Chemical compound C=1C=C2C=CC=CC2=CC=1OC(C)C(=O)NC1=CC=CC=C1 LVKTWOXHRYGDMM-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000005588 Oxadiazon Substances 0.000 description 1
- CHNUNORXWHYHNE-UHFFFAOYSA-N Oxadiazon Chemical compound C1=C(Cl)C(OC(C)C)=CC(N2C(OC(=N2)C(C)(C)C)=O)=C1Cl CHNUNORXWHYHNE-UHFFFAOYSA-N 0.000 description 1
- 235000001855 Portulaca oleracea Nutrition 0.000 description 1
- YLPGTOIOYRQOHV-UHFFFAOYSA-N Pretilachlor Chemical compound CCCOCCN(C(=O)CCl)C1=C(CC)C=CC=C1CC YLPGTOIOYRQOHV-UHFFFAOYSA-N 0.000 description 1
- OBLNWSCLAYSJJR-UHFFFAOYSA-N Quinoclamin Chemical compound C1=CC=C2C(=O)C(N)=C(Cl)C(=O)C2=C1 OBLNWSCLAYSJJR-UHFFFAOYSA-N 0.000 description 1
- KDWQYMVPYJGPHS-UHFFFAOYSA-N Thenylchlor Chemical group C1=CSC(CN(C(=O)CCl)C=2C(=CC=CC=2C)C)=C1OC KDWQYMVPYJGPHS-UHFFFAOYSA-N 0.000 description 1
- QHTQREMOGMZHJV-UHFFFAOYSA-N Thiobencarb Chemical compound CCN(CC)C(=O)SCC1=CC=C(Cl)C=C1 QHTQREMOGMZHJV-UHFFFAOYSA-N 0.000 description 1
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- MAHPNPYYQAIOJN-UHFFFAOYSA-N azimsulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N(N=CC=2C2=NN(C)N=N2)C)=N1 MAHPNPYYQAIOJN-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- HKPHPIREJKHECO-UHFFFAOYSA-N butachlor Chemical compound CCCCOCN(C(=O)CCl)C1=C(CC)C=CC=C1CC HKPHPIREJKHECO-UHFFFAOYSA-N 0.000 description 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- BWUPSGJXXPATLU-UHFFFAOYSA-N dimepiperate Chemical compound C=1C=CC=CC=1C(C)(C)SC(=O)N1CCCCC1 BWUPSGJXXPATLU-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- QMTNOLKHSWIQBE-FGTMMUONSA-N exo-(+)-cinmethylin Chemical compound O([C@H]1[C@]2(C)CC[C@@](O2)(C1)C(C)C)CC1=CC=CC=C1C QMTNOLKHSWIQBE-FGTMMUONSA-N 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 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
- 150000002576 ketones Chemical class 0.000 description 1
- XIGAUIHYSDTJHW-UHFFFAOYSA-N mefenacet Chemical compound N=1C2=CC=CC=C2SC=1OCC(=O)N(C)C1=CC=CC=C1 XIGAUIHYSDTJHW-UHFFFAOYSA-N 0.000 description 1
- HZDIJTXDRLNTIS-DAXSKMNVSA-N n-[[(z)-but-2-enoxy]methyl]-2-chloro-n-(2,6-diethylphenyl)acetamide Chemical compound CCC1=CC=CC(CC)=C1N(COC\C=C/C)C(=O)CCl HZDIJTXDRLNTIS-DAXSKMNVSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- ASRAWSBMDXVNLX-UHFFFAOYSA-N pyrazolynate Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OS(=O)(=O)C1=CC=C(C)C=C1 ASRAWSBMDXVNLX-UHFFFAOYSA-N 0.000 description 1
- VTRWMTJQBQJKQH-UHFFFAOYSA-N pyributicarb Chemical compound COC1=CC=CC(N(C)C(=S)OC=2C=C(C=CC=2)C(C)(C)C)=N1 VTRWMTJQBQJKQH-UHFFFAOYSA-N 0.000 description 1
- WRHZVMBBRYBTKZ-UHFFFAOYSA-N pyrrole-2-carboxylic acid Chemical compound OC(=O)C1=CC=CN1 WRHZVMBBRYBTKZ-UHFFFAOYSA-N 0.000 description 1
- FFSSWMQPCJRCRV-UHFFFAOYSA-N quinclorac Chemical compound ClC1=CN=C2C(C(=O)O)=C(Cl)C=CC2=C1 FFSSWMQPCJRCRV-UHFFFAOYSA-N 0.000 description 1
- MGLWZSOBALDPEK-UHFFFAOYSA-N simetryn Chemical compound CCNC1=NC(NCC)=NC(SC)=N1 MGLWZSOBALDPEK-UHFFFAOYSA-N 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000002054 transplantation Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は水稲用除草剤組成物
に関する。TECHNICAL FIELD The present invention relates to a herbicidal composition for paddy rice.
【0002】[0002]
【従来の技術および発明が解決しようとする課題】現
在、水稲用除草剤として数多くの化合物が実用化されて
いるが、既存の薬剤は移植水稲に薬害を及ぼすことな
く、対象雑草のみを選択的に防除するという要求を必ず
しも完全に満たすものではない。下記式(A)で表され
る化合物(一般名:ACN、キノクラミン、以下化合物
(A)と称する。)は藻類、ウキクサ等の防除に有効な
水稲用除草剤として既に実用化されている。また下記式
(B)で表される化合物(一般名:シハロホップブチ
ル、以下化合物(B)と称する。)は水稲用除草剤とし
て開発中の化合物であり、ノビエに対して特異的に高い
防除効果を有する。しかしながら当該化合物はノビエに
対して生育期処理効果は高いが、発芽前処理効果は低
い。またその他の水田広葉雑草に対する効果はない。2. Description of the Related Art At present, a number of compounds have been put into practical use as herbicides for paddy rice. However, existing chemicals do not cause harm to transplanted rice, and only select target weeds. Does not always completely meet the requirements for control. A compound represented by the following formula (A) (generic name: ACN, quinoclamin, hereinafter referred to as compound (A)) has already been put into practical use as a herbicide for paddy rice effective for controlling algae, duckweed and the like. In addition, a compound represented by the following formula (B) (generic name: cyhalofop-butyl, hereinafter referred to as compound (B)) is a compound under development as a herbicide for paddy rice, and is highly specific to Nobie. Has a controlling effect. However, while the compound has a high effect of treating the growing season with the growing season, it has a low effect of pre-emergence treatment. In addition, it has no effect on other weeds in paddy fields.
【0003】[0003]
【化2】 Embedded image
【0004】[0004]
【課題を解決するための手段】本発明者らは上記課題に
鑑み鋭意検討した結果、前記式(A)で表される化合物
と、式(B)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(以下本発明組成物と称す)が優れた
相乗作用を奏することをを見い出すにいたった。Means for Solving the Problems The present inventors have conducted extensive studies in view of the above problems, and as a result, contain a compound represented by the above formula (A) and a formula (B) as active ingredients. It has been found that the herbicide composition (hereinafter referred to as the composition of the present invention) having the above-mentioned composition exhibits an excellent synergistic effect.
【0005】本発明組成物では、化合物(B)に化合物
(A)を加えることにより、除草効果が単に相加的に得
られるだけでなく相乗的な効果が得られ、低薬量でノビ
エを完全に防除できる。In the composition of the present invention, by adding the compound (A) to the compound (B), not only the herbicidal effect can be obtained additively but also a synergistic effect can be obtained. It can be completely controlled.
【0006】[0006]
【発明の実施の形態】本発明組成物が好適な効果を示す
のは、化合物(A)1重量部当たり化合物(B)を0.
001〜100重量部含む場合であるが、化合物(A)
1重量部当たり化合物(B)を0.01〜10重量部含
む場合は更に好ましい効果が期待できる。BEST MODE FOR CARRYING OUT THE INVENTION The composition of the present invention exerts a preferable effect in that the compound (B) is added in an amount of 0.
001 to 100 parts by weight, the compound (A)
When 0.01 to 10 parts by weight of the compound (B) is included per 1 part by weight, more preferable effects can be expected.
【0007】本発明組成物の好適な処理薬量は、防除す
べき対象雑草の種類などにより左右されるが、有効成分
として化合物(A)が10g〜10kg/ha、化合物
(B)が1g〜10kgの場合であるが、化合物(A)
が1kg〜3kg/ha、化合物(B)が0.01kg
〜3kg/haの場合は更に好ましい効果が期待でき
る。The suitable treatment dose of the composition of the present invention depends on the kind of target weeds to be controlled, but the compound (A) is 10 g to 10 kg / ha and the compound (B) is 1 g to 1 g as the active ingredient. Compound (A) for 10 kg
1 kg to 3 kg / ha, compound (B) 0.01 kg
In the case of ~ 3 kg / ha, a more preferable effect can be expected.
【0008】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。本組成物は更に界面活性剤を含
むのが好ましい。本発明化合物は必要に応じて製剤また
は散布時に他種の除草剤、各種殺虫剤、殺菌剤、植物生
長調節剤、共力剤などと混合施用しても良い。The compositions according to the invention are preferably used in the form of compositions in which the active ingredient is mixed with a carrier which comprises a solid or liquid diluent. The composition preferably further comprises a surfactant. If necessary, the compound of the present invention may be mixed with other herbicides, various insecticides, fungicides, plant growth regulators, synergists and the like at the time of formulation or spraying.
【0009】特に、他の除草剤と混合施用することによ
り、施用薬量の減少による低コスト化、混合薬剤の相乗
作用による殺草スペクトラムの拡大や、より高い殺草効
果が期待できる。この際、同時に複数の公知除草剤との
組み合わせも可能である。本発明化合物と混合使用する
除草剤の種類としては、例えば、ファーム・ケミカルズ
・ハンドブック(Farm Chemicals Handbook)1993年
版に記載されている化合物などがある。[0009] In particular, by applying it in combination with other herbicides, it is expected that the cost can be reduced by reducing the amount of the applied drug, the herbicidal spectrum can be expanded by the synergistic action of the mixed drugs, and a higher herbicidal effect can be expected. At this time, a combination with a plurality of known herbicides is also possible at the same time. The types of herbicides used in combination with the compound of the present invention include, for example, the compounds described in Farm Chemicals Handbook, 1993 edition.
【0010】本発明化合物と混合使用するのに好ましい
薬剤としては、例えば、ピラゾスルフロンエチル(pyra
zosulfuron ethyl/一般名)、ベンスルフロンメチル
(bensulfuron methyl/一般名)、シノスルフロン(ci
nosulfuron/一般名)、イマゾスルフロン(imazosulfu
ron/一般名)、DPX−A8947(N-(((4,6-dimetho
xypyrimidin-2-yl)amino-carbonyl))-1-methyl-4-(2-me
thyl-2H-tetrazol-5-yl)-1H-pyrazole-5-sulfonamid
e)、プレチラクロール(pretilachlor/一般名)、エス
プロカルブ(esprocarb/一般名)、ピラゾレート(pyr
azolate/一般名)、ピラゾキシフェン(pyrazoxyfen/
一般名)、ベンゾフェナップ(benzofenap/一般名)、
ダイムロン(dymron/一般名)、ブロモブチド(bromob
utide/一般名)、ナプロアニリド(naproanilide/一
般名)、クロメプロップ(clomeprop/一般名)、CN
P(一般名)、クロメトキシニル(chlomethoxynil/一
般名)、ビフェノックス(bifenox/一般名)、オキサ
ジアゾン(oxadiazon/一般名)、メフェナセット(mef
enacet/一般名)、ブタクロール(butachlor/一般
名)、ブテナクロール(butenachlor/一般名)、ジチ
オピル(dithiopyr/一般名)、ベンフレセート(benfu
resate/一般名)、ピリブチカルブ(pyributicarb/一
般名)、ベンチオカーブ(benthiocarb/一般名)、ジ
メピペレート(dimepiperate/一般名)、モリネート
(molinate/一般名)、ブタミホス(butamifos/一般
名)、キンクロラック(quinclorac/一般名)、シンメ
チリン(cinmethylin/一般名)、シメトリン(simetry
n/一般名)、SAP(bensulide/一般名)、ジメタメ
トリン(dimethametryn/一般名)、MCPA、MCP
B、2’,3’−ジクロロ−4−エトキシメトキシベン
ズアリニド(試験名はHW−52)、1−(2−クロロ
ベンジル)−3−(α,α−ジメチルベンジル)尿素
(試験名はJC−940)、N−〔2’−(3’−メト
キシ)−チエニルメチル〕−N−クロロアセチル−2,
6−ジメチルアニリド(試験名はNSK−850)等が
あげられる。Examples of preferred agents to be used in combination with the compound of the present invention include pyrazosulfuron-ethyl (pyra).
zosulfuron ethyl / general name), bensulfuron methyl (bensulfuron methyl / generic name), sinosulfuron (ci
nosulfuron / generic name), imazosulfu
ron / generic name), DPX-A8947 (N-(((4,6-dimetho
xypyrimidin-2-yl) amino-carbonyl))-1-methyl-4- (2-me
thyl-2H-tetrazol-5-yl) -1H-pyrazole-5-sulfonamid
e), pretilachlor (generic name), esprocarb (generic name), pyrazolate (pyr)
azolate / generic name, pyrazoxifene /
(Generic name), benzophenap (generic name),
Dymron (generic name), bromobutide (bromob
utide / generic name), naproanilide / generic name, clomeprop / generic name, CN
P (generic name), clomethoxynil (generic name), bifenox (generic name), oxadiazon (generic name), mefenacet (mef)
enacet / generic name), butachlor / generic name, butenachlor / generic name, dithiopyr / generic name, benfrusate
resate / generic name, pyributicarb / generic name, benchiocarb / benthiocarb / generic name, dimepiperate / generic name, molinate / molinate / generic name, butamifos / butamifos / generic name, quinclorac / Generic name), cinmethylin (generic name), simetryn (simetry)
n / generic name), SAP (bensulide / generic name), dimethametryn (dimethametryn / generic name), MCPA, MCP
B, 2 ′, 3′-dichloro-4-ethoxymethoxybenzalinide (test name is HW-52), 1- (2-chlorobenzyl) -3- (α, α-dimethylbenzyl) urea (test name is JC-940), N- [2 '-(3'-methoxy) -thienylmethyl] -N-chloroacetyl-2,
6-dimethylanilide (test name is NSK-850) and the like.
【0011】本組成物を除草剤として施用するにあたっ
ては一般には適当な担体、例えばクレー、タルク、ベン
トナイト、珪藻土等の固体担体或いは水、アルコール類
(メタノール、エタノール等)、芳香族炭化水素類(ベ
ンゼン、トルエン、キシレン等)、塩素化炭化水素類、
エーテル類、ケトン類、エステル類(酢酸エチル等)、
酸アミド類(ジメチルホルムアミド等)などの液体担体
と混用して適用することができ、所望により乳化剤、湿
潤剤、分散剤、結合剤、浸透剤、展着剤、安定剤などを
添加し、乳剤、液剤、水和剤、粉剤、粒剤、顆粒水和
剤、フロアブル剤、錠剤等任意の剤型にて実用に供する
ことができる。In applying the present composition as a herbicide, generally, a suitable carrier, for example, a solid carrier such as clay, talc, bentonite, diatomaceous earth or the like, water, alcohols (methanol, ethanol, etc.), aromatic hydrocarbons ( Benzene, toluene, xylene, etc.), chlorinated hydrocarbons,
Ethers, ketones, esters (ethyl acetate etc.),
It can be applied by mixing it with a liquid carrier such as acid amides (dimethylformamide, etc.), and if desired, an emulsifier, a wetting agent, a dispersant, a binder, a penetrant, a spreading agent, a stabilizer, etc. are added to the emulsion. It can be put into practical use in any dosage form such as a liquid, a wettable powder, a powder, a granule, a wettable granule, a flowable tablet and a tablet.
【0012】この際同時に複数の他の除草剤、殺虫剤、
殺菌剤、植物生長調整剤、肥料等と混合使用することも
可能である。特に他の除草剤の1種あるいは2種以上を
配合することにより、殺草スペクトラムを広げることが
可能となり、本発明の効果をより安定なものとすること
ができる。At this time, a plurality of other herbicides, insecticides,
It is also possible to use it as a mixture with a fungicide, a plant growth regulator, a fertilizer and the like. In particular, by blending one or more other herbicides, the herbicidal spectrum can be broadened, and the effect of the present invention can be made more stable.
【0013】[0013]
【実施例】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、剤型等は実
施例のみに限定されるものではない。なお「部」は全て
重量部を意味する。 〔配合例1〕 粒剤 化合物(A) 5部 化合物(B) 1部 ベントナイト 55部 タルク 39部 以上を均一に混合粉砕した後、小量の水を加えて攪拌混
合捏和し、押出式造粒機で造粒し、乾燥して粒剤にす
る。EXAMPLES The present invention will be described in more detail with reference to the following examples, but the compounds, dosage amounts, dosage forms and the like in the present invention are not limited only to the examples. All “parts” mean parts by weight. [Compounding Example 1] Granules Compound (A) 5 parts Compound (B) 1 part Bentonite 55 parts Talc 39 parts After uniformly mixing and pulverizing the above, a small amount of water was added and the mixture was kneaded with stirring to form an extrusion type product. Granulate with a granulator and dry to give granules.
【0014】〔配合例2〕 顆粒水和剤(ドライフロア
ブル剤) 化合物(A) 50部 化合物(B) 20部 イソベンNo.1 10部 (アニオン性界面活性剤:クラレイソプレンケミカル
(株)商品名) バニレックスN 5部 (アニオン性界面活性剤:山陽国策パルプ(株)商品
名) カープレックス#80 15部 (ホワイトカーボン:塩野義製薬(株)商品名) 以上を均一に混合微粉砕してドライフロアブル剤とす
る。[Formulation Example 2] Granule wettable powder (dry flowable agent) Compound (A) 50 parts Compound (B) 20 parts Isoben No. 1 10 parts (anionic surfactant: Kuraray Isoprene Chemical Co., Ltd. trade name) Vanilex N 5 parts (anionic surfactant: Sanyo Kokusaku Pulp Co., Ltd. trade name) Carplex # 80 15 parts (white carbon: Shiono Gyosei Co., Ltd. trade name) The above is uniformly mixed and pulverized to obtain a dry flowable agent.
【0015】〔配合例3〕 水和剤 化合物(A) 50部 化合物(B) 2部 ジークライトPFP 41部 (カオリン系クレー:ジークライト工業(株)商品名) ソルポール5050 2部 (アニオン性界面活性剤:東邦化学工業(株)商品名) ノルックス1000C 3部 (アニオン性界面活性剤:東邦化学工業(株)商品名) カープレックス#80(固結防止剤) 2部 (ホワイトカーボン:塩野義製薬(株)商品名) 以上を均一に混合粉砕して水和剤とする。[Formulation Example 3] Wettable powder Compound (A) 50 parts Compound (B) 2 parts Dichlorite PFP 41 parts (Kaolin-based clay: product name of Siklite Industry Co., Ltd.) Solpol 5050 2 parts (anionic interface Activator: Toho Chemical Industry Co., Ltd. trade name Norx 1000C 3 parts (Anionic surfactant: Toho Chemical Industry Co., Ltd. trade name) Carplex # 80 (anti-caking agent) 2 parts (White Carbon: Shionogi Pharmaceutical Co., Ltd. trade name) The above is uniformly mixed and pulverized to obtain a wettable powder.
【0016】除草剤混合物の相乗的除草効果についは、
次のように説明することができる。即ち、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種の除草剤の安定組合せにより期待される活性
は、次のように計算することができる。(コルビー(C
olby S.R.)、除草剤の組合せの相乗および拮
抗作用反応の計算、ウィード(Weed)、第15巻、
20〜22頁(1967年)を参照) E=α+β−(α・β/100) 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。Regarding the synergistic herbicidal effect of the herbicide mixture,
It can be explained as follows. That is, an individual active compound often shows a defect in its herbicidal activity, but in that case, the herbicidal activity obtained by combining two active compounds is a simple sum of the respective activities of the two compounds ( When it is larger than the expected activity), this is called synergism. The expected activity of a stable combination of two herbicides can be calculated as follows. (Colby (C
olby S. R. ), Calculation of synergistic and antagonistic responses of herbicide combinations, Weed, vol. 15,
See pages 20 to 22 (1967). E = α + β- (α · β / 100) α: Inhibitory rate when herbicide A is treated with a dose of akg / ha β: Herbicide B with bkg / ha Inhibition rate when treated with different amounts E: Herbicide A is akg / ha, Herbicide B is bkg / ha
Inhibition rate expected when treated with the amount of i.e., that is, if the actual inhibition rate is larger than the above calculation, it can be said that the activity by the combination shows a synergistic effect.
【0017】次に本発明組成物の除草剤としての有用性
を以下の試験例において具体的に説明する。 〔試験例1〕 ノビエ発芽前における除草効果試験 1/5000アールのワグネルポットに沖積土壌を入れ
た後、水を入れて混和し、水深4cmの湛水条件とし
た。ノビエの種子を播種し、2.5葉期の葉齢のイネ苗
を2cmの深さで移植した。イネ移植翌日に、前記処方
に準じて試製した水和剤を用いて供試薬剤の所定濃度の
懸濁液をメスピペットで滴下処理した。薬剤処理後3週
間目に各雑草およびイネの地上部生体重を測定し、次の
式で抑制率(%)を求めた。Next, the usefulness of the composition of the present invention as a herbicide will be specifically described in the following test examples. [Test Example 1] Herbicidal effect test before novier germination After alluvial soil was placed in a Wagner pot of 1/5000 are, water was added to mix, and the water was submerged under a depth of 4 cm. The seeds of Novier were sown, and rice seedlings having a leaf age of 2.5 leaves were transplanted at a depth of 2 cm. On the day after rice transplantation, a suspension of the test reagent having a predetermined concentration was dropped using a wet pipette using a wettable powder prepared according to the above formulation. Three weeks after the chemical treatment, the above-ground fresh weight of each weed and rice was measured, and the inhibition rate (%) was calculated by the following formula.
【0018】抑制率(%)=(1−処理区の地上部生体
重/無処理区の地上部生体重)×100 結果を第1表および第2表に示す。なお以下、表中の記
号は以下を表す。 a:ノビエ、r:イネ 〔試験例2〕 ノビエ2.5葉期における除草効果試験 1/5000アールのワグネルポット中に沖積土壌を入
れた後、水を入れて混和し、水深4cmの湛水条件とし
た。ノビエの種子を播種し、2.5葉期に生育した時点
で前記処方に準じて試製した水和剤を用いて、供試薬剤
の所定濃度の懸濁液をメスピペットで滴下処理した。薬
剤処理後3週間目に地上部の生体重を測定し、前述試験
例1と同様に抑制率(%)を求めた。結果を第3表およ
び第4表に示す。なお、表中の記号は試験例1と同様で
ある。Inhibition rate (%) = (1-above-ground fresh weight of treated area / above-ground fresh weight of untreated area) × 100 The results are shown in Tables 1 and 2. In the following, the symbols in the table represent the following. a: Novier, r: Rice [Test Example 2] Herbicidal effect test in Nobie 2.5 leaf stage After alluvial soil was put in a 1/5000 are Wagner pot, water was added to mix it, and a water depth of 4 cm was applied. It was a condition. The seeds of Novier were sown, and at the time of growth at the 2.5 leaf stage, a wettable powder prepared in accordance with the above formulation was used to drop a suspension of the reagent at a predetermined concentration with a measuring pipette. The body weight of the above-ground part was measured 3 weeks after the chemical treatment, and the inhibition rate (%) was determined in the same manner as in Test Example 1 above. The results are shown in Tables 3 and 4. The symbols in the table are the same as in Test Example 1.
【0019】[0019]
【表1】 第1表 単剤の除草効果(抑制率%) ────────────────────────────── 有効成分 草 種 化合物 の処理量 ──────────────────── (g/ha) a r ────────────────────────────── (A) 500 10 0 ────────────────────────────── (B) 50 70 0 100 80 0 150 90 0 ────────────────────────────── [Table 1] Table 1 Herbicidal effect of single agent (inhibition rate%) ────────────────────────────── Throughput of seed compound ──────────────────── (g / ha) ar ─────────────────── ──────────── (A) 500 100 ────────────────────────────── (B ) 50 70 0 100 80 0 150 90 90 ───────────────────────────────
【0020】[0020]
【表2】 第2表 混合剤の除草効果の実測値と期待値(抑制率%) ────────────────────────────────── 各有効 草 種 化合物 成分の a r 処理量 ──────────────────────── (g/ha) (F) (E) (F) (E) ────────────────────────────────── (A)+(B) 500+50 100 73 0 0 (A)+(B) 500+100 100 82 0 0 (A)+(B) 500+150 100 91 0 0 ────────────────────────────────── (但し、表中、(E)はコルビーの式から求めた抑制率の
期待値を示し、(F)は実測値を示す。また各有効成分の
処理量の欄の向かって左側の数値及び右側の数値はそれ
ぞれ化合物名の欄の化合物の対応する薬量を表す。第4
表の記載もこれに準ずる。)[Table 2] Table 2 Measured value and expected value (inhibition rate%) of the herbicidal effect of the admixture ──────────────────────────── ─────── ar processing amount of each effective herbaceous compound component ──────────────────────── (g / ha) (F) (E) (F) (E) ────────────────────────────────── (A) + (B) 500 + 50 100 73 0 0 (A) + (B) 500 + 100 100 82 0 0 (A) + (B) 500 + 150 100 91 0 0 ─────────────── ─────────────────── (However, in the table, (E) shows the expected value of the suppression rate obtained from the Colby equation, and (F) shows the measured value. The numbers on the left side and the numbers on the right side of the column of the amount of each active ingredient treated represent the corresponding doses of the compounds in the column of the compound name, respectively.
The description in the table follows this. )
【0021】[0021]
【表3】 [Table 3]
【0022】[0022]
【表4】 第4表 混合剤の除草効果の実測値と期待値(抑制率%) ─────────────────────────── 各有効 草 種 化合物 成分の a r 処理量 ───────────────── (g/ha) (F) (E) (F) (E) ─────────────────────────── (A)+(B) 500+50 100 82 0 0 (A)+(B) 500+100 100 91 0 0 (A)+(B) 500+150 100 100 0 0 ─────────────────────────── [Table 4] Table 4 Measured and expected values (inhibition rate%) of the herbicidal effect of the mixture ──────────────────────────── Ar processing amount of each effective herbaceous compound component ────────────────── (g / ha) (F) (E) (F) (E) ───── ────────────────────── (A) + (B) 500 + 50 100 82 0 0 (A) + (B) 500 + 100 100 91 0 0 (A) + (B) 500 + 150 100 100 0 0 ───────────────────────────
【0023】[0023]
【発明の効果】本発明組成物はノビエに対し優れた相乗
効果を奏する。The composition of the present invention exerts an excellent synergistic effect on Nobie.
Claims (3)
(B)で表される化合物とからなる組成物。 【化1】 1. A composition comprising a compound represented by the following formula (A) and a compound represented by the following formula (B). Embedded image
と、式(B)で表される化合物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。2. A herbicidal composition comprising a compound represented by formula (A) according to claim 1 and a compound represented by formula (B) as active ingredients.
と、式(B)で表される化合物とを同時に使用すること
を特徴とする除草方法。3. A herbicidal method comprising using the compound represented by the formula (A) according to claim 1 and the compound represented by the formula (B) at the same time.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6452096A JPH09255508A (en) | 1996-03-21 | 1996-03-21 | Herbicidal composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6452096A JPH09255508A (en) | 1996-03-21 | 1996-03-21 | Herbicidal composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH09255508A true JPH09255508A (en) | 1997-09-30 |
Family
ID=13260584
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6452096A Pending JPH09255508A (en) | 1996-03-21 | 1996-03-21 | Herbicidal composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH09255508A (en) |
-
1996
- 1996-03-21 JP JP6452096A patent/JPH09255508A/en active Pending
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