TW200808182A - Herbicide composition - Google Patents

Herbicide composition Download PDF

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TW200808182A
TW200808182A TW096119225A TW96119225A TW200808182A TW 200808182 A TW200808182 A TW 200808182A TW 096119225 A TW096119225 A TW 096119225A TW 96119225 A TW96119225 A TW 96119225A TW 200808182 A TW200808182 A TW 200808182A
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component
herbicidal composition
herbicidal
mass
compound
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TW096119225A
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TWI382815B (en
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Yoshihiro Yamaji
Shuji Ohno
Yasunori Ogawa
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Kumiai Chemical Industry Co
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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/541,3-Diazines; Hydrogenated 1,3-diazines
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/18Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
    • A01N37/22Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/36Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
    • A01N37/38Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
    • A01N37/40Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N39/00Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
    • A01N39/02Aryloxy-carboxylic acids; Derivatives thereof
    • A01N39/04Aryloxy-acetic acids; Derivatives thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N41/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
    • A01N41/02Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
    • A01N41/10Sulfones; Sulfoxides
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/36Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/561,2-Diazoles; Hydrogenated 1,2-diazoles
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/64Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/661,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
    • A01N43/681,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms with two or three nitrogen atoms directly attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/74Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
    • A01N43/761,3-Oxazoles; Hydrogenated 1,3-oxazoles
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/90Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/12Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N63/00Biocides, pest repellants or attractants, or plant growth regulators containing microorganisms, viruses, microbial fungi, animals or substances produced by, or obtained from, microorganisms, viruses, microbial fungi or animals, e.g. enzymes or fermentates
    • A01N63/30Microbial fungi; Substances produced thereby or obtained therefrom

Abstract

Disclosed is a herbicide which has a high activity against undesirable weeds growing in a habitat of a cultivated plant, a wide herbicidal spectrum, an excellent residual efficacy, and high safety for a cultivated plant. More specifically, disclosed is a herbicidal composition comprising: (A) a compound selected from a difluoromethane sulfonylanilide compound represented by the general formula (I) and a salt thereof; and (B) at least one member selected from pyraclonil, imazosulfuron, seprocarb, metamifop, triaziflam, pyrazoxyfen, 2,4-D, etobenzanid, mesotrione, tefuryltrione and a herbicidal microorganism, as active ingredients. (I) wherein R1 represents a hydrogen atom, an alkyl group having 1 to 6 carbon atoms or an alkoxyalkyl group having 2 to 6 carbon atoms.

Description

200808182 (1) 九、發明說明 【發明所屬之技術領域】 本發明係有關,栽培植物例如農作物的栽培之際,爲 選擇去除不期望的雜草,將2種或其以上之除草活性化合 ~ 物組合的新穎除草用組成物及使用之雜草的控制方法者。 【先前技術】 φ 在農業領域,爲生產性之提升及省力化,自早期以來 即使用除草劑,目前爲止,因應栽培作物、去除之雜草的 種類,已開發各種各樣之除草劑。就此除草劑而言,以相 對於栽培植物沒有不良影響,而且儘可能相對於多數種類 之雜草有效者;即,具有廣闊之殺草光譜者爲佳。 不過,近年來,經過長時間使用同種類之除草劑的結 果,相對於除草劑,具有耐性而難以去除之雜草增加,再 加上由於農藥的大量使用,環境污染成爲社會問題,期望 φ 對此等具有耐性之雜草有效,且以低藥量亦能顯示充分的 效果之高活性除草劑。 ^ 另一方面,爲儘量控制起因於每一種農作物或雜草之 生育時期所使用的不同除草劑之土質劣化、且對應於經過 長時間使用而起之雜草的不整齊生長,更期望殘效性良好 、且經過自雜草之生長前至生育期止的長時間’能發揮效 力之長時間持續型的除草劑。 進而,就除草劑而言,使用之際’由於氣象條件’例 如溫度之高低、風之有無、太陽光之強弱等;土壤條件, -6 - (2) 200808182 例如土壤組成、有機物含量等;栽培條件’例如移植深度 、水深等;除草劑之施用條件,例如散佈不均勻、過量散 佈等;對農作物造成藥害。更期待藉由如此之條件的改變 •,出現對農作物不產生藥害之除草劑。 &quot; 另外之方面,將2種化合物組合,進行改良以單獨之 « 化合物作爲有效成份的除草劑之缺點。例如作爲改善相對 於水田顯示廣闊之殺草光譜的磺醯基替苯胺衍生物之水稻 p 的安全性,有將水稻用除草劑與眾所周知的化合物組合混 合而成之除草劑組成物(JP2000-28 1 5 1 3A);單獨使用時 ,不得不以高濃度使用之故,對水稻有不良影響,有在 2-〔 (4,6-二甲氧基嘧啶-2-基)羥基甲基〕-6-甲氧基甲 基-N-二氟甲院磺醯基苯胺中,與 orthobencarb、 bensulide、asulam、propanil等作爲除草劑之有效成份的 化合物組合,改良其缺點之除草劑組成物 ( W02004/01 0784A1)等的提案。 φ 不過,此等除草劑組成物,不能充分滿足上述期望事 項之全部;進而,顯示優越效果之除草劑組成物的開發, . 成爲農業領域之重要課題。 【發明內容】 本發明以提供,改善以往除草劑之上述缺點,具有廣 闊之殺草光譜、同時相對於雜草顯示高活性、殘效性優越 、且相對於栽培植物具有高安全性之除草組成物爲目的。 本發明的工作同仁,爲達成上述種種期望而開發除草 (3) 200808182 劑,經深入探討不斷硏究之結果發現,以一般式所示之二 氟甲院磺醯基替苯胺化合物或其鹽、與具有除草性之特定 化合物的組合作爲有效成份而含有之除草用組成物,在稻 作、旱作、園藝栽培、矮草育成之際,可經長時間防止並 去除多種不期望之雜草的生長,且相對於栽培植物顯示高 安全性’並且在發芽前及發芽後均能發揮此效果,以此見 識爲基準完成本發明。 即,本發明提供一種除草用組成物,其特徵爲含有: (A) 以選自該一般式(1)所示之二氟甲烷磺醯基替 苯胺化合物或其鹽之化合物(成份A )、與 (B) 選自 pyraclonil、imazo sulfuron、esprocarb、 metamifop 、 triaziflam 、 pyr azoxy fen 、 2,4-D 、 etobenzanid、mesotrion、tefuryltrione 及除草用微生物之200808182 (1) EMBODIMENT OF THE INVENTION [Technical Fields According to the Invention] The present invention relates to the cultivation of planting plants such as crops, in order to selectively remove unwanted weeds, and to combine two or more herbicidal activities. The combination of the novel herbicidal composition and the method of controlling the weed used. [Prior Art] φ In the agricultural field, for the improvement of productivity and labor saving, herbicides have been used since the early days. So far, various herbicides have been developed in response to the types of cultivated crops and weeds removed. In the case of this herbicide, it has no adverse effect with respect to cultivated plants, and is as effective as possible with respect to most kinds of weeds; that is, it is preferred to have a broad spectrum of herbicidal. However, in recent years, after using the same kind of herbicide for a long time, the weeds which are resistant to being difficult to remove relative to the herbicide increase, and the environmental pollution becomes a social problem due to the large-scale use of the pesticide, and it is expected that φ These highly active weeds are effective and can exhibit sufficient effects as high active herbicides at low doses. ^ On the other hand, it is more desirable to control the deterioration of the soil caused by the different herbicides used in the growth period of each crop or weed, and to correspond to the irregular growth of weeds that have been used for a long time. A long-lasting herbicide that is good and can be used for a long time from the growth of weeds to the growth period. Further, in the case of herbicides, the use of 'weather conditions' such as temperature, presence or absence of wind, strong sunlight, etc.; soil conditions, -6 - (2) 200808182 such as soil composition, organic matter content, etc.; cultivation Conditions 'such as transplant depth, water depth, etc.; herbicide application conditions, such as uneven distribution, excessive dispersion, etc.; cause phytotoxicity to crops. It is expected that by such changes in conditions, there will be herbicides that do not cause phytotoxicity to crops. &quot; On the other hand, the combination of the two compounds is modified to separate the shortcomings of the herbicide as a compound. For example, as a herbicide composition which is a mixture of a herbicide for rice and a well-known compound, it is used as a herbicide composition for improving the safety of a rice sulfonate aniline derivative which exhibits a broad spectrum of herbicidal activity in a paddy field (JP2000-28) 1 5 1 3A); when used alone, it has to be used at a high concentration, which has an adverse effect on rice, and is in 2-[(4,6-dimethoxypyrimidin-2-yl)hydroxymethyl]- 6-methoxymethyl-N-difluoromethyl sulfonyl aniline, combined with orthobencarb, bensulide, asulam, propanil, etc. as an active ingredient of a herbicide, to improve its disadvantages of herbicide composition (W02004/ 01 0784A1) and other proposals. φ However, these herbicide compositions do not fully satisfy all of the above-mentioned desired matters; further, the development of herbicide compositions exhibiting superior effects has become an important issue in the agricultural field. SUMMARY OF THE INVENTION The present invention provides a herbicidal composition which has the above-mentioned disadvantages of the herbicide, has a broad herbicidal spectrum, exhibits high activity relative to weeds, has excellent residual effect, and has high safety with respect to cultivated plants. for purpose. The work of the present invention, in order to achieve the above various expectations, the development of weeding (3) 200808182 agent, after intensive investigation and continuous research results, found in the general formula of the difluoromethyl sulfonyl anilide compound or its salt, The herbicidal composition contained as an active ingredient in combination with a specific compound having herbicidal properties can prevent and remove various undesired weeds over a long period of time in rice cultivation, dry farming, horticultural cultivation, and dwarf grass breeding. The present invention can be carried out based on the knowledge that it grows and shows high safety with respect to cultivated plants' and can exert this effect before and after germination. That is, the present invention provides a herbicidal composition comprising: (A) a compound (ingredient A) selected from the group consisting of a difluoromethanesulfonylanilide compound represented by the general formula (1) or a salt thereof, And (B) selected from pyraclonil, imazo sulfuron, esprocarb, metamifop, triaziflam, pyr azoxy fen, 2,4-D, etobenzanid, mesotrion, tefuryltrione and weed microbes

至少一種(成份B)爲有效成份;及使用此除草用組成物 ,在農作物栽培區域控制不期望之雜草的產生或成長之方 法。 R1At least one (ingredient B) is an active ingredient; and a method of controlling the production or growth of undesirable weeds in a crop growing area using the herbicidal composition. R1

(I) (式中之R1爲氫原子、碳數1〜6之烷基或碳數2〜 6之烷氧基烷基)。 本發明之作爲成份A使用的該一般式(I)所示之二 氟甲烷磺醯基替苯胺化合物,單獨具有除草活性( -8- (4) 200808182 JP2000-44546A )。 另一方面,pyraclonil、tefury Itrione、imazo sulfuron 、 halosulfuron-methyl 、 esprocarb 、 oxadiazon 、 met ami fop 、 cumy luron 、 clomazone 、 triaziflam 、 penoxsulam 、 pyr azoxyfen 、 2,4-D 、 MCP A 、 cyclosulfamuron 、 azimsulfuron 、 etobenzanid 、(I) (wherein R1 is a hydrogen atom, an alkyl group having 1 to 6 carbon atoms or an alkoxyalkyl group having 2 to 6 carbon atoms). The difluoromethanesulfonyl anilide compound of the general formula (I) used in the present invention as the component A has herbicidal activity alone (-8-(4) 200808182 JP2000-44546A). On the other hand, pyraclonil, tefury Itrione, imazo sulfuron, halosulfuron-methyl, esprocarb, oxadiazon, met ami fop, cumy luron, clomazone, triaziflam, penoxsulam, pyr azoxyfen, 2,4-D, MCP A, cyclosulfamuron, azimsulfuron, etobenzanid ,

ethoxy sulfuron 、 cinosulfuron 、 flucetosulfuron 、 pyribenzoxim、mesotrion等,構成相對於共通的雜草顯示 除草活性之群。〔例如「The Pesticide Manual」等第 13 版,2004 年(British Crop Protection Council 發行)及 「AG CHEM New compound Review 2006」(AGRANOVA 發行)〕。 不過,本發明由上述群中特SU選出 pyraclonil、 imazo sulfuron 、 esprocarb 、 metamifop 、 triaziflam 、 pyrazoxyfen 、 2 5 4 - D 、 etobenzanid 、 mesotrion 、 及 tefuryltrione,與成份A組合使用爲其特徵。又,除草用 微生物亦可與此等同樣使用。 藉由將上述之成份A及成份B兩者組合使用,可發 揮其相乘效果;分別單獨使用時,不能獲所期望之廣範圍 的殺草光譜,經長期間之雜草的生育控制效果及栽培植物 保護之故的充分安全性。 本發明之成份A的一般式(I )所示化合物中之R1, 爲氫原子、碳數1〜6之直鏈或支鏈的烷基或碳數2〜6之 直鏈或支鏈的烷氧基烷基。烷基以甲基、乙基、丙基、異 -9- 200808182 (5) 丙基、丁基、異丁基、仲丁基、叔丁基、戊基、1-甲基丁 基、己基寺爲佳5以乙基更適合。院氧基院基以甲氧基甲 基、甲氧基乙基、乙氧基乙基'3-乙氧基丙基、1-甲基- 3-甲氧基丁基等爲佳,以甲氧基甲基更適合。 ^ 又,一般式(I )所示之二氟甲烷磺醯基替苯胺化合 • 物或其鹽,亦可與選自 halosulfuron-methyl、oxadiazon、 cumyluron 、 clomazone 、 penoxsulam 、 MCPA 、 cyclosulfamuron 、 azimsulfuron 、 ethoxy sulfuron 、 cinosulfuron、flucetosulfuron、pyribenzoxim 等之至少一 種化合物混合使用。 另一方面,成份 B 必要爲選自 pyraclonil、 imazosulfuron 、 esprocarb 、 metamifop 、 triaziflam 、 pyrazoxyfen 、 2,4-d 、 etobenzanid 、 mesotrion 、 tefuryltrione及除草用微生物。藉由此等與成份A之組合 ,與單獨使用時之除草效果比較,其顯現快,進而可獲得 φ 由單獨使用時之除草效果所不能預測的高除草效果或寬廣 之殺草光譜。不過,爲上述成份B以外之化合物時,例如 • 單獨顯示可與上述化合物匹敵之除草性者,藉由與成份A 組合得不到相乘效果。 又,除草用微生物,例如 Drechslera monoceras ( MTB-951株),亦同樣可與成份A組合使用。將此等2 種以上混合使用亦能獲得良好的除草效果。 本發明之除草用組成物,可將例如在水田所生長之一 年生雜草的田犬稗(Echinochloa oryzicola)、犬稗( -10 - 200808182 ⑹ rEthoxysulfonon, cinosulfuron, flucetosulfuron, pyribenzoxim, mesotrion, etc., constitute a group exhibiting herbicidal activity relative to common weeds. [13th edition such as "The Pesticide Manual", 2004 (issued by the British Crop Protection Council) and "AG CHEM New compound Review 2006" (AGRANOVA issued). However, the present invention is characterized in that pyraclonil, imazo sulfuron, esprocarb, metamifop, triaziflam, pyrazoxyfen, 2 5 4 -D, etobenzanid, mesotrion, and tefuryltrione are selected from the above-mentioned group, and are used in combination with component A. Further, the microorganism for weeding can be used in the same manner as these. By combining the above-mentioned component A and component B, the synergistic effect can be exerted; when used alone, the desired wide range of herbicidal spectrum can not be obtained, and the growth control effect of weeds over a long period of time and Adequate safety for the protection of cultivated plants. R1 in the compound of the general formula (I) of the component A of the present invention is a hydrogen atom, a linear or branched alkyl group having 1 to 6 carbon atoms or a linear or branched alkyl group having 2 to 6 carbon atoms. Alkoxy group. Alkyl group is methyl, ethyl, propyl, iso-9- 200808182 (5) propyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, 1-methylbutyl, hexyl temple For better 5, ethyl is more suitable. The methoxy group is preferably methoxymethyl, methoxyethyl, ethoxyethyl '3-ethoxypropyl, 1-methyl-3-methoxybutyl, etc. Oxymethyl groups are more suitable. ^ Further, the difluoromethanesulfonyl anilide compound or its salt represented by the general formula (I) may also be selected from the group consisting of halosulfuron-methyl, oxadiazon, cumyluron, clomazone, penoxsulam, MCPA, cyclosulfamuron, azimsulfuron, ethoxy At least one compound of sulfuron, cinosulfuron, flucetosulfuron, pyrimibenzoxim or the like is used in combination. On the other hand, the component B is preferably selected from the group consisting of pyraclonil, imazosulfuron, esprocarb, metamifop, triaziflam, pyrazoxyfen, 2,4-d, etobenzanid, mesotrion, tefuryltrione and herbicidal microorganisms. By this combination with the component A, it exhibits a faster appearance than the herbicidal effect when used alone, and thus a high herbicidal effect or a broad herbicidal spectrum which cannot be predicted by the herbicidal effect when used alone can be obtained. However, when it is a compound other than the above-mentioned component B, for example, the herbicidal which is comparable to the above compound is displayed alone, and the synergistic effect is not obtained by combining with the component A. Further, a microorganism for weeding, such as Drechslera monoceras (plant MTB-951), can also be used in combination with component A. A good herbicidal effect can also be obtained by mixing these two or more types. The herbicidal composition of the present invention may be, for example, Echinochloa oryzicola or canine scorpion which grows one of the annual weeds in the paddy field (-10 - 200808182 (6) r

Echinochlo crus-galli var. crus-galli)等之野稗類、玉莎 草(Cyperus difformis )、雛莎草(Cyperus flaccidus ) 等莎草類,小水葱(Monochoria vaginalis)、水葵( Monochoria korsakowii)等水葵科雜草、畔草類、畔枷( Dopatrium junceum)等胡麻葉草科雜草、木程草(Rotala indica)、姬溝萩(Ammannia multiflora)等溝萩科雜草 、溝繁縷(Elatine Uiandra )等及多年生雜草之瓜皮( Sagittaria pygmaea)、澤瀉(Sagittaria trifolia)等澤瀉 科雜草、水莎草(Cyperus serotinus )、螢藺(Scirpus nipponicus )、黑慈薛(Eleocharis kuroguwai )、犬螢( S cirpus juncoides ) 、黑三稜(Scirpus planiculmis ) 、松 葉 (Eleocharis aciculairis ) 等莎草科雜草、蛭蓆 ( Potamogeton distinctus )、水斧(O en ant he j avanica )等 、又如草地、田地、果樹園中之野稗類、雌日芝類、狗尾 草類、雀帷子(Poa annua)、雄曰芝(Eleusine indica ) 等稻科雜草、姬女黃(Erigeron annuus)、春女毙( Eriger on philadelphicus ) 、大野塘蒿(Erigeron floribundus)等之菊科雜草、浜萱(Cyperus rotundus) 、水蜈松(Ccyperus brevifolius )、莎草(Cyperus microiria ) 等莎草科雜草、耳葉草 (Cerastium holosteoides)、繁蔞(Stellaria media)等瞿麥科雜草、 地錦類之胡麻葉草科雜草、大犬蓼(P〇lyg〇num )、羊蹄 等之蓼科雜草、青莧(Amaranthus viridis )、犬莧( Amaranthus lividus)等莧科雜草、露草(Commelina -11 - (7) (7)200808182 communis )、九葉露草(Commelina benghalensis )等之 露草科雜草、杉菜(Equisetum arvense )、犬杉葉f Equi-setum palustre)等之砥草科雜草、錦草類之澤漆科 雜草、止血草類之芹科雜草等,在其自發芽前至生育期之 廣闊範圍予以防止去除;相對於栽培植物顯示高安全性。 還有’於此所謂「栽培植物」,包含藉由育種法或遺傳因 子工程之方法,相對於除草劑或除草劑群具耐性者。 本發明之除草用組成物,依對象場地、對象作物、所 不期望之雜草種類或雜草之狀態、散佈時期、散佈方法、 製劑型等而異,因應需求可在廣闊範圍改變混合比例、营女 佈量。 配合比例,一般而言以質量比計,相對於成份A之1 質量份,成份B爲0.1〜2,000質量份、較佳爲 0.2〜 1,500質量份、最佳爲在0.5〜1,000質量份之範圍內配合 〇 又,本發明之除草用組成物,因應需求亦可混用殺蟲 劑、殺菌劑、其他之除草劑、植物生長調節劑、微生物、 肥料等。 本發明之除草用組成物,使用時可使用其有效成份本 身,因應需求,可含有農藥製劑中通常所使用之添加成份 〇 此添加成份有,固體載體或液體載體等載體、界面活 性劑、黏合劑、黏著賦予劑、增黏劑、著色劑、擴展劑、 展著劑、防凍劑、防固劑、崩壞劑、防分解劑等等。 -12- (8) (8)200808182 其他,因應需求亦可將防腐劑、或植物片等作爲添加 成份使用。 上述之固體載體有,例如石英、黏土、高嶺石、葉蜡 石、絹雲母、滑石、膨潤土、酸性白土、綠坡縷石、沸石 、矽藻土等天然礦物質類;碳酸鈣、硫酸銨、硫酸鈉、氯 化鉀等無機鹽類;合成矽酸、合成矽酸鹽、澱粉、纖維素 、植物粉末等有機固體載體;聚乙烯、聚丙烯、聚偏氯乙 烯等塑料載體等。此等可單獨使用,亦可2種以上組合使 用。 液體載體有,例如甲醇、乙醇、丙醇、異丙醇、丁醇 等一元醇類,或乙二醇、二乙二醇、丙二醇、己二醇、聚 乙二醇、聚丙二醇、丙三醇等多元醇類等醇類;丙烯系二 醇醚等多元醇系化合物類;丙酮、甲乙酮、甲異丁酮、二 異丁酮、環己酮等酮類;乙醚、二噁烷、乙二醇單乙醚、 二丙醚、四氫呋喃等醚類;正烷烴、環烷、異烷烴、媒油 、礦油等脂肪族烴類;苯、甲苯、二甲苯、溶劑石腦油、 烷基萘等芳香族烴類;二氯乙烷、三氯甲烷、四氯化碳等 鹵化烴類;乙酸乙酯、苯二甲酸二異丙基酯、苯二甲酸二 丁酯、苯二甲酸二辛酯、己二酸二甲酯等酯類;r-丁內 酯等內酯類;二甲基甲醯胺、二乙基甲醯胺、二甲基乙醯 胺、N-烷基吡咯烷酮等醯胺類;乙腈等腈類;二甲基亞碾 等硫化合物類;大豆油、菜子油、棉籽油、篦麻油等植物 油;水等。此等可單獨使用,亦可2種以上組合使用。 界面活性劑有,例如山梨糖醇酐脂肪酸酯、聚環氧乙 -13- 200808182 (9) 烷山梨糖醇酐脂肪酸酯、蔗糖脂肪酸酯、聚環氧乙烷脂肪 酸酯、聚環氧乙烷樹脂酸酯、聚環氧乙烷脂肪酸二酯、聚 環氧乙烷烷基醚、聚環氧乙烷烷基苯基醚、聚環氧乙烷二 烷基苯基醚、聚環氧乙烷烷基苯基醚甲醛縮合物、聚環氧 产 乙烷聚環氧丙烷嵌段聚合物、烷基聚環氧乙烷聚環氧丙烷 - 嵌段聚合物醚、聚環氧乙烷烷基胺、聚環氧乙烷脂肪酸醯 胺、聚環氧乙烷脂肪酸雙苯基醚、聚環氧烷苄基苯基醚、 φ 聚環氧烷苯乙烯基苯基醚、乙炔二醇、聚環氧烷加成乙炔 二醇、聚環氧乙烷醚型聚矽氧、酯型聚矽氧、氟系界面活 性劑、聚環氧乙烷蓖麻油、聚環氧乙烷硬化蓖麻油等非離 子性界面活性劑;烷基硫酸鹽、聚環氧乙烷烷基醚硫酸鹽 、聚環氧乙烷烷基苯基醚硫酸鹽、聚環氧乙烷苯乙烯基苯 基醚硫酸鹽、烷基苯磺酸鹽、木質素磺酸鹽、烷基磺基琥 珀酸鹽、萘磺酸鹽、烷基萘磺酸鹽、萘磺酸之甲醛縮合物 之鹽、烷基萘磺酸之甲醛縮合物之鹽、脂肪酸鹽、多羧酸 φ 鹽、N-甲基脂肪酸肌氨酸酯、樹脂酸鹽、聚環氧乙烷烷基 醚磷酸鹽、聚環氧乙院院基苯基醚磷酸鹽等陰離子性界面 _ 活性劑;(十二)烷基胺鹽酸鹽、(十八)烷基胺鹽酸鹽 、油基胺鹽酸鹽、(十八)烷基胺乙酸鹽、(十八)烷基 胺基丙基胺乙酸鹽、烷基三甲基銨氯化物、烷基二甲基氯 化苄烷銨等烷基胺鹽等陽離子界面活性劑;胺基酸型或甜 菜鹼型等兩性界面活性劑等。 此等界面活性劑可單獨使用,亦可2種以上組合使用 -14- (10) (10)200808182 黏合劑或黏著賦予劑有,例如羧甲基纖維素或其鹽、 糊精、水溶性澱粉、三仙膠、瓜耳豆膠、蔗糖、聚乙儲( 基)吡咯院酮、阿拉伯膠、聚乙烯醇、聚乙烯乙酸酯、聚 丙嫌酸鈉、平均分子量6,0 0 0〜2 0,0 0 〇之聚乙二醇、平均 分子量10萬〜500萬之聚環氧乙院、磷脂質(例如腦磷 脂、卵磷脂等)等。 增黏劑有,例如三仙膠、瓜耳豆膠、羧甲基纖維素、 聚乙烯吡咯烷酮、羧基乙烯基聚合物、丙烯酸系聚合物、 澱粉系化合物及水溶性多醣類等水溶性高分子、高純度膨 潤土、煙燻二氧化矽等無機微粉等。 著色劑有,例如氧化鐵、氧化鈦、普魯士藍等無機顏 料;茜素染料、偶氮染料、金屬酞菁染料等有機染料。 擴展劑有,例如聚矽氧系界面活性劑、纖維素粉末、 糊精、加工澱粉、多胺基羧酸鉗化合物、交聯聚乙烯吡咯 烷酮、順丁烯二酸與苯乙烯類之共聚物、(甲基)丙烯酸 系共聚物、由多元醇所成之聚合物與二羧酸酐之半酯、聚 苯乙烯磺酸之水溶性鹽等。 展著劑有,例如石蠟、萜烯、聚醯胺樹脂、聚丙烯酸 鹽、聚環氧乙烷、蠟、聚乙烯基烷基醚、烷基酚甲醛縮合 物、合成樹脂乳膠等。 防凍劑有,例如乙二醇、二乙二醇、丙二醇、丙三醇 等多元醇類等。 防固劑有,例如澱粉、褐藻酸、甘露糖、半乳糖等多 醣類;聚乙烯吡咯烷酮、煙燻二氧化矽、酯膠、石油樹脂 -15- (11) 200808182 等。 崩壞劑有’例如三聚磷酸鈉、六偏磷酸 屬鹽、纖維素粉末、糊精、甲基丙烯酸酯系 乙烯吡咯烷酮、多胺基羧酸鉗合化合物、磺 丁烯·順丁烯二酸酐共聚物、澱粉•聚丙烯 等。 防分解劑有,例如沸石、生石灰、氧化 水楊酸系、二苯甲酮系等紫外線吸收劑等。 防腐劑有,例如山梨酸鉀、1,2 -苯並噻口 植物片有,例如鋸屑、椰子殼、玉蜀黍 等。 本發明之除草用組成物中含有上述添加 有比例以質量爲基準,載體通常爲5〜9 5 % 9 0 % ;界面活性劑通常爲〇 · 1〜3 0 %、較佳焉 其他之添加劑爲〇 · 1〜3 0 %、較佳爲在〇 . 5〜 擇。 本發明之除草用組成物,可進行製劑化 、水合劑、粉劑、油劑、顆粒水合劑、可流 、粒劑、微粒劑、巨型劑、懸浮乳膠、微膠 型而使用。 在此製劑化時,亦可作爲與成份A及届 農藥、例如其他之除草劑、殺蟲劑、殺菌劑 節劑、或肥料等之混合組成物。 本發明之除草用組成物,在使用之際, 鈉、硬脂酸金 之共聚物、聚 化苯乙燒•異 腈接枝共聚物 鎂等乾燥劑; 坐啉-3-酮等。 穗軸、煙草莖 成份時,其含 、較佳爲2 0〜 ! 0.5 〜1 0 % ; 1 0 %之範圍選 爲液劑、乳劑 動劑、懸浮劑 囊等隨意之劑 2份B以外之 、植物成長調 亦可直接施用 -16- 200808182 (12) ,或因應使用目的稀釋濃度’藉由莖葉散佈、土壤施用或 水面施用而使用。又,本發明之除草用組成物,亦可預先 混合而使用,亦可因應目的依順序使用。 本發明之除草用組成物的製劑中之有效成份量,可因 ^ 應需求適當選擇。作爲粉劑、微粒劑或粒劑時,爲0.0 1〜 • 8 0重量%、較佳爲自0.0 5〜5 0重量%之範圍選擇。又,作 爲乳劑、液劑、可流動劑、水合劑及顆粒水合劑時,爲1 φ 〜90重量%、較佳爲自5〜80重量%之範圍選擇。 本發明之除草用組成物的施用量,依含有之有效成份 的種類、對象雜草、產生傾向、環境條件、所使用之製劑 的劑型等而改變, 於粉劑、微粒劑或粒劑之情況,每1 〇公畝,有效成 份爲0.18〜51^、較佳爲自0.58〜1]^之範圍選擇使用。 於乳劑、液劑、可流動劑、水合劑或顆粒水合劑等之 情況,以水稀釋使用時,使用之有效成份濃度一般自1〇 ^ 〜100,0 00ppm之範圍選擇使用。 _ 〔用以實施發明之最佳形態〕 其次,以實施例說明本發明之最佳形態。有效成份、 添加劑之種類及配合比率,並非僅限定於此等’可在廣闊 範圍改變。又,下述例中之化合物A-1,係一般式(ί ) 中之R1爲甲氧基甲基的化合物之pyrimisulfan。即,2-〔 (4,6_二甲氧基嘧啶-2-基)羥基甲基〕-6-甲氧基甲基-N-二氟甲烷磺醯基替苯胺。 -17- (13)200808182 還有,下述說明中之「部」爲質量份。 【實施方式】 〔實施例1〕 將化合物A-1 Pyraclonil 聚環氧乙烷辛基苯基醚 /3 -萘磺酸甲醛縮合物鈉鹽 矽藻土 及、黏土 混合粉碎,即得水合劑。 1質量份 7質量份 0.5質量份 〇. 5質量份 20質量份 7 1質量份 〔實施例2〕 將化合物A-1 Tefuryltrione 聚環氧乙烷辛基苯基醚 冷-萘磺酸甲醛縮合物鈉鹽 砂藻土 及、黏土 混合粉碎,即得水合劑。 1質量份 1 〇質量份 0.5質量份 0.5質量份 20質量份 6 8質量份 〔實施例3〕 將化合物A -1 Mesotrion 1質量份 1 〇質量份 -18- (14)200808182 聚環氧乙烷辛基苯基醚 0.5質量伤 /3 -萘磺酸甲醛縮合物鈉鹽 〇 . 5質量伤 矽藻土 2 〇質量份 及、碳酸鈣 68質量份 混合粉碎,即得水合劑。 〔實施例4〕 將化合物A -1 1 〇質量份 T efuryltrione 1 〇質量份 木質素磺酸鈉 5質量份 聚環氧乙烷烷基芳基醚 1質量份 聚羧酸鈉 3質量份 白碳黑 5質量份 α化澱粉 1質量份 碳酸鈣 65質量份 及、水 1 〇質量份 混煉進行押出造粒。將所得粒狀物以流動層乾燥機乾燥 即得顆粒水合劑。 〔實施例5〕 將水 62.9質量 化合物A -1 5質量份 Mesotrion 1 5質量份 木質素磺酸鈉 2質量份 -19- 200808182 (15) 聚環氧乙院院基芳基醚硫酸錢 4質量份 聚環氧乙烷烷基芳基醚 0.5質量份 三仙膠 0.1質量份 膨潤土 0.5質量份 - 及、乙二醇 1 0質量份 以高速攪拌機混合,以濕式粉碎機粉碎,即得可流動劑 ^ 〔實施例6〕 將化合物A-1 1質量份 P y r a c 1 ο n i 1 滑石與膨潤土以1 : 3之比例混合的 7質量份 增量劑 7 7質量份 白碳黑 1 0質量份 界面活性劑聚環氧乙烷山梨糖醇酐烷基 化物、聚環氧乙烷烷基芳基聚合物及烷 φ 基芳基磺酸酯之混合物 5質量份 及、水 1 0質量份 加入,將經混煉爲糊狀者自直徑1 mm之篩網押出,經乾 燥後切成〇 . 5〜1 mm之長度,即得粒劑。 其次,以試驗例說明本發明之除草用組成物的效果。 〔試驗例1〕(於水田之除草效果試驗) 在1/2000公畝之塑料容器中塡充水田土壤,施肥、混 勻後,播種田犬稗(Eo; Echinochloa oryzoides)、小水 • 20 - 200808182 (16) 葱(Mo; Monochoria vaginalis )、犬營(Sc; Scirpus juncoides)、水竹葉(An; Aneilema keisak)之各種子, 及將莎草(Cs; Cyperus serotinus)之塊莖埋入水深lcm。 又,在同一容器中將水稻(Or )移植,於溫室內育成。其 • 後,在田犬稗(Eo )達到2.5葉期之階段,沉入水中3cm深 • ,將以實施例1爲基準而調製之水合劑的所定量以水稀釋 ,施用於水面。其後維持沉入水中深度3cm予以育成;處 φ 理第25天之除草效果及藥害程度,以表1所示之基準爲指 數表示。結果如表2所示。還有,藥量係每10公畝之有效 成份量。 表1 指數 除草效果及藥害程度(地上部份之生育抑制度) 10 95%以上之生育抑制 9 85%以上95%未滿之生育抑制 8 75%以上85%未滿之生育抑制 7 65%以上75%未滿之生育抑制 6 55%以上65%未滿之生育抑制 5 45%以上55%未滿之生育抑制 4 35%以上45%未滿之生育抑制 3 25%以上35%未滿之生育抑制 2 15%以上25%未滿之生育抑制 1 5%以上15%未滿之生育抑制 _ 0 5%未滿之生育抑制 -21 - (17)200808182Echinochlo crus-galli var. crus-galli) such as wild pheasant, Cyperus difformis, Cyperus flaccidus, etc., sedge, Monochoria vaginalis, Monochoria korsakowii Such as water weedy weeds, grasses, pupa (Dopatrium junceum) and other flax weeds, Rotala indica, Ammannia multiflora and other gully weeds, ditch (缕) Elatine Uiandra ) and other perennial weeds (Sagittaria pygmaea), Sagittaria trifolia, etc., genus Lycopene, Cyperus serotinus, Scirpus nipponicus, Eleocharis kuroguwai ), Scirpus juncoides, Scirpus planiculmis, Eleocharis aciculairis, sedge weeds, Potamogeton distinctus, O en ant he j avanica, etc. Such as grassland, fields, orchards in the orchard, female Japanese hordes, foxtails, Poa annua, Eleusine indica, etc., rice weeds, Erigeron annuus, spring Eriger on philadelphicus, Erigeron floribundus, cypress weeds, Cyperus rotundus, Ccyperus brevifolius, Cyperus microiria, etc. Certicium holosteoides, Stellaria media, weeds, weeds, weeds, P〇lyg〇num, sheepshoes, etc. Amaranthus viridis, Amaranthus lividus, and other weeds, cedars (Commelina -11 - (7) (7) 200808182 communis), and Commelina benghalensis Equisetum arvense), yew leaf f Equi-setum palustre, etc., such as weeds, weeds, weeds, weeds, weeds, weeds, etc. The range is prevented from being removed; it shows high safety relative to cultivated plants. Further, the term "cultivated plants" herein includes those resistant to herbicides or herbicides by methods of breeding or genetic engineering. The herbicidal composition of the present invention varies depending on the target site, the target crop, the type of undesired weeds or weeds, the distribution period, the dispersion method, the preparation type, etc., and the mixing ratio can be changed in a wide range according to the demand. Camp female cloth volume. The compounding ratio is generally 0.1 to 2,000 parts by mass, preferably 0.2 to 1,500 parts by mass, preferably 0.5 to 1,000 parts by mass, based on 1 part by mass of the component A. In addition, the herbicidal composition of the present invention may be mixed with an insecticide, a bactericide, other herbicides, plant growth regulators, microorganisms, fertilizers, etc., depending on the requirements. The herbicidal composition of the present invention can be used as the active ingredient itself, and can contain the additive component usually used in the pesticide preparation according to the demand, and the added component is a carrier such as a solid carrier or a liquid carrier, a surfactant, and a binder. Agents, adhesion-imparting agents, tackifiers, colorants, extenders, spreading agents, antifreeze agents, anti-solid agents, breakers, anti-decomposition agents, and the like. -12- (8) (8)200808182 Others, preservatives, or plant flakes can be used as an additive in response to demand. The above solid carrier has natural minerals such as quartz, clay, kaolinite, pyrophyllite, sericite, talc, bentonite, acid white clay, attapulgite, zeolite, diatomaceous earth, calcium carbonate, ammonium sulfate, Inorganic salts such as sodium sulfate and potassium chloride; organic solid carriers such as citric acid, synthetic citrate, starch, cellulose, and plant powder; plastic carriers such as polyethylene, polypropylene, and polyvinylidene chloride. These may be used singly or in combination of two or more. The liquid carrier is, for example, a monohydric alcohol such as methanol, ethanol, propanol, isopropanol or butanol, or ethylene glycol, diethylene glycol, propylene glycol, hexanediol, polyethylene glycol, polypropylene glycol, glycerol. Alcohols such as polyols; polyol compounds such as propylene glycol ether; ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, diisobutyl ketone, and cyclohexanone; diethyl ether, dioxane, and ethylene glycol. Ethers such as monoethyl ether, dipropyl ether and tetrahydrofuran; aliphatic hydrocarbons such as n-alkanes, naphthenes, isoalkanes, kerosenes, mineral oils; aromatics such as benzene, toluene, xylene, solvent naphtha, alkyl naphthalene Hydrocarbons; halogenated hydrocarbons such as dichloroethane, chloroform, carbon tetrachloride; ethyl acetate, diisopropyl phthalate, dibutyl phthalate, dioctyl phthalate, hexane Esters such as dimethyl acid ester; lactones such as r-butyrolactone; decylamines such as dimethylformamide, diethylformamide, dimethylacetamide, N-alkylpyrrolidone; acetonitrile Such as nitriles; dimethyl sulfite and other sulfur compounds; soybean oil, rapeseed oil, cottonseed oil, castor oil and other vegetable oil; water and so on. These may be used alone or in combination of two or more. Surfactants include, for example, sorbitan fatty acid esters, polyepoxyethylene-13-200808182 (9) sorbitan fatty acid esters, sucrose fatty acid esters, polyethylene oxide fatty acid esters, polycyclic rings Oxyethane resin acid ester, polyethylene oxide fatty acid diester, polyethylene oxide alkyl ether, polyethylene oxide alkyl phenyl ether, polyethylene oxide dialkyl phenyl ether, poly ring Oxyethane alkyl phenyl ether formaldehyde condensate, polyepoxy ethane polypropylene oxide block polymer, alkyl polyethylene oxide polypropylene oxide - block polymer ether, polyethylene oxide Alkylamine, polyethylene oxide fatty acid decylamine, polyethylene oxide fatty acid bisphenyl ether, polyalkylene oxide benzyl phenyl ether, φ polyalkylene oxide styryl phenyl ether, acetylene glycol, Polyalkylene oxide addition acetylene glycol, polyethylene oxide ether type polyoxynium oxide, ester type polyfluorene oxide, fluorine-based surfactant, polyethylene oxide castor oil, polyethylene oxide hardened castor oil, etc. Nonionic surfactant; alkyl sulfate, polyethylene oxide alkyl ether sulfate, polyethylene oxide alkyl phenyl ether sulfate, polyethylene oxide benzene Salt of formaldehyde condensate of alkenylphenyl ether sulfate, alkylbenzenesulfonate, lignosulfonate, alkylsulfosuccinate, naphthalenesulfonate, alkylnaphthalenesulfonate, naphthalenesulfonic acid a salt of a formaldehyde condensate of an alkylnaphthalenesulfonic acid, a fatty acid salt, a polycarboxylic acid φ salt, an N-methyl fatty acid sarcosinate, a resinate, a polyethylene oxide alkyl ether phosphate, a polyepoxy Anionic interface such as phenyl ether phosphate in hospital, _ active agent; (d) alkylamine hydrochloride, (octadecylalkylamine hydrochloride, oleylamine hydrochloride, (18) a cationic surfactant such as an alkylamine salt such as an alkylamine acetate, an (octadecyl)alkylaminopropylamine acetate, an alkyltrimethylammonium chloride or an alkyldimethylbenzylammonium chloride; An amphoteric surfactant such as an amino acid type or a betaine type. These surfactants may be used singly or in combination of two or more. 14-(10) (10)200808182 Binders or adhesion-imparting agents such as carboxymethylcellulose or a salt thereof, dextrin, water-soluble starch , Sanxianjiao, guar gum, sucrose, polyethylidene (pyridyl), gum arabic, polyvinyl alcohol, polyvinyl acetate, polyacrylic acid sodium, average molecular weight 6,0 0 0~2 0 , 0 0 聚 polyethylene glycol, an average molecular weight of 100,000 to 5 million poly epoxy enamel, phospholipids (such as cephalin, lecithin, etc.). Examples of tackifiers include water-soluble polymers such as Sanxian gum, guar gum, carboxymethyl cellulose, polyvinylpyrrolidone, carboxyvinyl polymer, acrylic polymer, starch compound, and water-soluble polysaccharide. Inorganic fine powder such as high-purity bentonite and smoked cerium oxide. Examples of the coloring agent include inorganic pigments such as iron oxide, titanium oxide, and Prussian blue; and organic dyes such as halogen dyes, azo dyes, and metal phthalocyanine dyes. Examples of the extender include, for example, a polyoxyn surfactant, a cellulose powder, a dextrin, a processed starch, a polyaminocarboxylic acid tong compound, a crosslinked polyvinylpyrrolidone, a copolymer of maleic acid and styrene, A (meth)acrylic copolymer, a half ester of a polymer made of a polyhydric alcohol, a dicarboxylic acid anhydride, or a water-soluble salt of polystyrenesulfonic acid. Exhibitors include, for example, paraffin wax, terpene, polyamide resin, polyacrylate, polyethylene oxide, wax, polyvinyl alkyl ether, alkylphenol formaldehyde condensate, synthetic resin emulsion, and the like. Examples of the antifreezing agent include polyhydric alcohols such as ethylene glycol, diethylene glycol, propylene glycol, and glycerin. Anti-solid agents include, for example, polysaccharides such as starch, alginic acid, mannose, and galactose; polyvinylpyrrolidone, fumed ceria, ester gum, and petroleum resin -15-(11) 200808182. The breakers are, for example, sodium tripolyphosphate, hexametaphosphate, cellulose powder, dextrin, methacrylate vinylpyrrolidone, polyaminocarboxylic acid clamp compound, sulfonbutene maleic anhydride Copolymer, starch, polypropylene, etc. Examples of the anti-decomposition agent include ultraviolet absorbers such as zeolite, quicklime, oxidized salicylic acid, and benzophenone. Preservatives include, for example, potassium sorbate, 1,2-benzothiazole, such as sawdust, coconut shell, maize, and the like. The herbicidal composition of the present invention contains the above-mentioned added ratio, and the carrier is usually 5 to 95% by weight based on the mass; the surfactant is usually 〇1 to 30%, preferably 焉 other additives are 〇·1~3 0 %, preferably in 〇. 5~ 择. The herbicidal composition of the present invention can be used in the form of a formulation, a hydrating agent, a powder, an oil agent, a granule hydrating agent, a flowable agent, a granule, a microparticle, a giant agent, a suspension latex, and a microgel type. In the case of this formulation, it may also be a mixed composition with the component A and the pesticide, for example, other herbicides, insecticides, fungicides, fertilizers, and the like. The herbicidal composition of the present invention is a desiccant such as sodium, a copolymer of gold stearate, a poly(phenylene bromide), an isocyanide graft copolymer, or the like; a sucrose-3-one or the like. When the cob and tobacco stem components are contained, the content thereof is preferably from 0 0 to 0.5 to 1 0%; the range of 10% is selected as a liquid agent, an emulsion agent, a suspension agent bag, and the like, 2 parts of B or the like. Plant growth can also be directly applied -16-200808182 (12), or used according to the purpose of dilution concentration 'by stem and leaf spread, soil application or surface application. Further, the herbicidal composition of the present invention may be used in advance by mixing, or may be used in order according to the purpose. The amount of the active ingredient in the preparation of the herbicidal composition of the present invention can be appropriately selected depending on the demand. When it is used as a powder, a microparticle or a granule, it is selected from the range of 0.01 to 80% by weight, preferably from 0.05 to 5% by weight. Further, in the case of an emulsion, a liquid agent, a flowable agent, a hydrating agent and a particulate hydrating agent, it is selected from the range of 1 φ to 90% by weight, preferably from 5 to 80% by weight. The application amount of the herbicidal composition of the present invention varies depending on the kind of the active ingredient contained, the target weed, the tendency to produce, the environmental conditions, the dosage form of the preparation to be used, and the like, in the case of a powder, a microparticle or a granule, For every 1 〇 acre, the effective ingredient is 0.18~51^, preferably from 0.58~1]^. In the case of emulsions, liquids, flowables, hydrating agents or granule hydrating agents, when used in water dilution, the concentration of the active ingredient used is generally selected from the range of 1 〇 〜 100 00 ppm. _ [Best Mode for Carrying Out the Invention] Next, the best mode of the present invention will be described by way of examples. The type of the active ingredient and the additive and the compounding ratio are not limited to these, and can be changed in a wide range. Further, the compound A-1 in the following examples is a pyrimisulfan compound of a compound of the formula (ί) wherein R1 is a methoxymethyl group. Namely, 2-[(4,6-dimethoxypyrimidin-2-yl)hydroxymethyl]-6-methoxymethyl-N-difluoromethanesulfonylaniline. -17- (13)200808182 In addition, the "parts" in the following description are parts by mass. [Embodiment] [Example 1] A compound A-1 Pyraclonil polyethylene oxide octyl phenyl ether / 3 - naphthalene sulfonic acid formaldehyde condensate sodium salt diatomaceous earth and clay were mixed and pulverized to obtain a hydrating agent. 1 part by mass of 7 parts by mass of 0.5 parts by mass of ruthenium. 5 parts by mass of 20 parts by mass of 7 parts by mass [Example 2] Compound A-1 Tefuryltrione Polyethylene oxide octyl phenyl ether cold-naphthalenesulfonic acid formaldehyde condensate The sodium salt diatomaceous earth and clay are mixed and pulverized to obtain a hydrating agent. 1 part by mass of 1 part by mass of 0.5 part by mass of 0.5 part by mass of 20 parts by mass of 6 parts by mass [Example 3] Compound A -1 Mesotrion 1 part by mass of 1 part by mass of -18-(14)200808182 polyethylene oxide Octyl phenyl ether 0.5 mass damage / 3 - naphthalene sulfonic acid formaldehyde condensate sodium salt 5. 5 mass 矽 矽 algae 2 〇 mass parts and 68 parts by mass of calcium carbonate are mixed and pulverized to obtain a hydrating agent. [Example 4] Compound A -1 1 〇 parts by mass of Tefuryltrione 1 〇 by mass of sodium lignin sulfonate 5 parts by mass of polyethylene oxide alkyl aryl ether 1 part by mass of sodium polycarboxylate 3 parts by mass of white carbon 5 parts by mass of black gelatinized starch, 1 part by mass of 65 parts by mass of calcium carbonate, and 1 part by mass of water, kneaded and granulated. The obtained granules were dried in a fluidized bed dryer to obtain a granule hydrating agent. [Example 5] Water 62.9 mass of compound A -1 5 parts by mass of Mesotrion 1 5 parts by mass of sodium lignin sulfonate 2 parts by mass - 19 - 200808182 (15) Poly epoxy compound aryl ether ether sulfuric acid money 4 mass Part by weight of polyethylene oxide alkyl aryl ether 0.5 parts by mass of Sanxian gum 0.1 parts by mass of bentonite 0.5 parts by mass - and 10 parts by mass of ethylene glycol are mixed by a high speed mixer and pulverized by a wet pulverizer to obtain a flowable Agent ^ [Example 6] Compound A-1 1 part by mass of P yrac 1 ο ni 1 talc and bentonite in a ratio of 1:3, 7 parts by mass of extender, 7 parts by mass of white carbon black, 10 parts by mass of interface 5 parts by mass of a mixture of an active agent polyethylene oxide sorbitan alkylate, a polyethylene oxide alkyl aryl polymer and an alkyl aryl sulfonate, and 10 parts by mass of water, added After being kneaded into a paste, it is extruded from a sieve having a diameter of 1 mm, and after drying, it is cut into a length of 5 to 1 mm, that is, a granule is obtained. Next, the effects of the herbicidal composition of the present invention will be described by way of test examples. [Test Example 1] (Testing the weeding effect in paddy fields) Fill the paddy soil in a plastic container of 1/2000 acre, fertilize and mix, and sow the field dog E (Eo; Echinochloa oryzoides), Xiaoshui • 20 - 200808182 (16) Onion (Mo; Monochoria vaginalis), dog camp (Sc; Scirpus juncoides), water bamboo leaves (An; Aneilema keisak), and the sedge (Cs; Cyperus serotinus) tubers buried in water depth lcm . Further, rice (Or) was transplanted in the same container and bred in a greenhouse. After that, in the stage where the dog cockroach (Eo) reached the 2.5-leaf stage, it was submerged in water to a depth of 3 cm. The amount of the hydrating agent prepared on the basis of Example 1 was diluted with water and applied to the water surface. Thereafter, the depth of the submerged water was maintained at a depth of 3 cm to be bred; the herbicidal effect and the degree of phytotoxicity on the 25th day were indicated by the index shown in Table 1. The results are shown in Table 2. Also, the dose is the effective amount per 10 acres. Table 1 Index herbicidal effect and degree of phytotoxicity (fertility of the above-ground part) 10 95% or more of birth inhibition 9 85% or more 95% less than the growth inhibition 8 75% or more 85% less than the birth inhibition 7 65% More than 75% of the above-mentioned birth inhibition 6 55% or more 65% less than the birth inhibition 5 45% or more 55% less than the birth inhibition 4 35% or more 45% less than the birth inhibition 3 25% or more 35% less than Fertility inhibition 2 15% or more 25% less than the birth inhibition 1 5% or more 15% less than the birth inhibition _ 0 5% under the birth inhibition-21 - (17)200808182

表2 供試除草劑 藥量 除草效1 3 藥害 g ai/lOa Eo Mo Sc Cs An Or 化合物A-1 + 0 + 20 9 9 6 5 8 0 3 + 0 9 8 9 8 2 0 Pyraclonil 3 + 20 10 10 10 10 10 0 化合物A-1 + 0 + 30 3 10 8 6 9 0 3 + 0 9 8 9 8 2 0 Tefuryltrione 3 + 30 10 10 10 10 10 0 化合物A-1 + 0 + 9 3 8 8 8 2 0 3 + 0 9 8 9 8 2 0 Imazosulfuron 3 + 9 10 10 10 10 3 0 化合物A-1 + 0+150 10 4 5 1 7 0 3 + 0 9 8 9 8 2 0 Esprocarb 3 + 150 10 10 10 10 9 0 化合物A-1 + 0 + 20 10 0 0 0 0 0 3 + 0 9 8 9 8 2 0 Metamifop 3 + 20 10 9 9 9 2 0 化合物A-1 + 0 + 10 8 9 5 2 7 0 3 + 0 9 8 9 8 2 0 Triaziflam 3 + 10 10 10 10 10 10 0 化合物A-1 + 0+180 5 10 6 5 9 0 3 + 0 9 8 9 8 2 0 Pyxazoxyfen 3 + 180 10 10 10 10 10 0 化合物A-1 + 0 + 45 1 10 4 1 10 0 3 + 0 9 8 9 8 2 0 2,4-D 3 + 45 10 10 10 10 10 0 化合物A-1 + 0 + 150 9 5 2 1 5 0 3 + 0 9 8 9 8 2 0 Etobenzanid 3 + 150 10 10 10 10 10 0 化合物A-1 + 0 + 9 3 7 8 5 9 0 3 + 0 9 8 9 8 2 0 Mesotrion 3 + 9 10 10 10 10 10 0 -22- 200808182 (18) 〔試驗例2〕(於水田之除草效果試驗) 在1/20 00公畝之塑料容器中塡充水田土壤,施肥、 混勻後,播種田犬稗(Eo )、小水葱(Mo )、犬螢(Sc )、水竹葉(An)之各種子,及將莎草(Cs)之塊莖埋入 ‘ 水深1cm。又,在同一容器中將水稻(〇r )移植,於溫室 • 內育成。其後,在田犬稗(Eo )達到2葉期之階段,沉入 水中10 cm,調製MTB-951株之分生子爲2.5xl01G個/10 φ 公畝’混合於以實施例1爲基準調製之化合物A-1的水合 劑之所定量以水稀釋的散佈液中,施用於水面。其後維持 沉入水中深度l〇cm予以育成。處理第25天之除草效果 及藥害程度,以表1所示之基準爲指數表示。結果如表3 所示。藥量之單位,化合物A-1爲「g ai/10a」、MTB-951株爲「個/ l〇a」。 表 供試除草劑 化合物A-1 + MTB-951 株 藥量 除草效身 | 藥害 Eo Mo Sc Cs An Or 0 + 2.5xl010 7 0 0 0 0 0 3 + 0 9 9 9 8 4 0 3 + 2.5xl010 10 10 10 10 5 0 〔試驗例3〕(於直播水田之莖葉處理除草效果試驗) 在1/10,000公畝之塑料容器中塡充水田土壤,施肥 、混勻後,播種水稻(〇r )、犬稗(Ec; Echinochloa crus-galli var. crus-galli ) 、睦茅 (L e ; Lepo ch 1 o a chinensis Nees)、莎草(Cy; Cyperus difformis)之各種 -23- (19) 200808182 子。其後,於溫室內育成;在水稻(Or )、犬稗(Ec)、 莎草(Cy )到達4葉期,哇茅(Le )到達5-6葉期時’將 以實施例1爲基準而調製之水合劑的所定量以水稀釋’於 化合物A-1中調整展著劑界面活性劑爲散佈水量之0.1% ,在植物體全體進行莖葉處理。其後,處理2天後沉入水 中深度爲3 cm,於溫室內育成;處理第3 0天之除草效果 及樂害程度’以表1所不之基準爲指數表TfC。結果如表4 所示。藥量爲每一公頃之有效成份量。 表4 供試除草劑 供試藥量 除草效果 藥害 g ai/ha Ec Le Cy Or 化合物A-1 + 5 + 25 9 7 10 0 10 + 50 10 10 10 0 Metamifop 20 + 100 10 10 10 0 25 6 6 0 0 Metamifop 50 10 7 0 0 100 10 10 1 0 5 4 1 10 0 化合物A_1 10 7 6 10 0 20 8 7 10 0Table 2 Test herbicide herbicide herbicidal effect 1 3 Phytotoxicity g ai/lOa Eo Mo Sc Cs An Or Compound A-1 + 0 + 20 9 9 6 5 8 0 3 + 0 9 8 9 8 2 0 Pyraclonil 3 + 20 A 10 + 10 + 10 3 8 8 2 0 3 + 0 9 8 9 8 2 0 Imazosulfuron 3 + 9 10 10 10 10 3 0 Compound A-1 + 0+150 10 4 5 1 7 0 3 + 0 9 8 9 8 2 0 Esprocarb 3 + 150 10 10 10 10 9 0 Compound A-1 + 0 + 20 10 0 0 0 0 0 3 + 0 9 8 9 8 2 0 Metamifop 3 + 20 10 9 9 9 2 0 Compound A-1 + 0 + 10 8 9 5 2 7 0 3 + 0 9 8 9 8 2 0 Triaziflam 3 + 10 10 10 10 10 10 0 Compound A-1 + 0+180 5 10 6 5 9 0 3 + 0 9 8 9 8 2 0 Pyxazoxyfen 3 + 180 10 10 10 10 10 0 Compound A-1 + 0 + 45 1 10 4 1 10 0 3 + 0 9 8 9 8 2 0 2,4-D 3 + 45 10 10 10 10 10 0 Compound A-1 + 0 + 150 9 5 2 1 5 0 3 + 0 9 8 9 8 2 0 Etobenzanid 3 + 150 10 10 10 10 10 0 A-1 + 0 + 9 3 7 8 5 9 0 3 + 0 9 8 9 8 2 0 Mesotrion 3 + 9 10 10 10 10 10 0 -22- 200808182 (18) [Test Example 2] (Weeding effect in paddy fields) Test) Fill the paddy soil in a plastic container of 1/20 00 acre, fertilize and mix, and sow the field dog (Eo), small water onion (Mo), canine (Sc), water bamboo leaves (An ) various kinds of seeds, and buried the tuber of sedge (Cs) into a water depth of 1cm. In addition, rice (〇r) was transplanted in the same container and bred in a greenhouse. Thereafter, in the stage where the dog bark (Eo) reached the 2-leaf stage, it was submerged in water to 10 cm, and the meristematic number of the MTB-951 strain was 2.5xl01G/10 φ acre mixed with the formulation of Example 1 as a reference. The hydrating agent of the compound A-1 was applied to the surface of the water in a dispersion liquid diluted with water. Thereafter, the depth of the submerged water was maintained at a depth of l〇cm to be bred. The herbicidal effect and the degree of phytotoxicity on the 25th day of treatment were expressed as indices on the basis shown in Table 1. The results are shown in Table 3. The unit of the dose, the compound A-1 is "g ai/10a", and the MTB-951 strain is "one / l〇a". Table test herbicide compound A-1 + MTB-951 strain herbicidal effect | phytotoxicity Eo Mo Sc Cs An Or 0 + 2.5xl010 7 0 0 0 0 0 3 + 0 9 9 9 8 4 0 3 + 2.5 Xl010 10 10 10 10 5 0 [Test Example 3] (Testing the herbicidal effect of stems and leaves in live water fields) Fill the paddy soil in a plastic container of 1/10,000 acre, fertilize and mix, and plant rice (〇r ), canine (Ec; Echinochloa crus-galli var. crus-galli), 睦 ( (L e; Lepo ch 1 oa chinensis Nees), sedge (Cy; Cyperus difformis) of various -23- (19) 200808182 . Thereafter, it is bred in a greenhouse; when rice (Or), canine (Ec), sedge (Cy) reaches the 4-leaf stage, and wow (Le) reaches the 5-6-leaf stage, 'will be based on Example 1 The amount of the hydrated agent to be prepared is diluted with water. In the compound A-1, the spreading agent surfactant is adjusted to 0.1% of the amount of water dispersed, and the whole plant body is subjected to stem and leaf treatment. Thereafter, after 2 days of treatment, the depth of sinking into the water was 3 cm, which was bred in a greenhouse; the herbicidal effect and the degree of toxicity on the 30th day of treatment were based on the index table TfC. The results are shown in Table 4. The dose is the amount of active ingredient per hectare. Table 4 Herbicides for test herbicide herbicidal effect phytotoxicity g ai/ha Ec Le Cy Or Compound A-1 + 5 + 25 9 7 10 0 10 + 50 10 10 10 0 Metamifop 20 + 100 10 10 10 0 25 6 6 0 0 Metamifop 50 10 7 0 0 100 10 10 1 0 5 4 1 10 0 Compound A_1 10 7 6 10 0 20 8 7 10 0

〔試驗例4〕(藉由莖葉處理之除草效果試驗) 在1 /1 0,0 0 0公畝之塑料容器中塡充旱地土壤,播種 盤固草(Di; Digitaria ciliaris)之種子,由容器底部給水 。於溫室內育成;盤固草(Di )到達5葉期時’將以實施 例1爲基準而調製之水合劑的所定量以水稀釋,在植物體 全體進行莖葉處理。其後’再於玻璃室內育成;處理後第 -24- 200808182 (20) 3 〇天之除草效果及藥害程度,以表1之基準爲指數表示 。結果如表5所示。藥量爲每一公頃之有效成份量。 表5 供試除草劑 供試藥量 除草效果 g ai/ha Di 5 + 25 9 化合物 A-1 + Metamifop 10 + 50 10 20 + 100 10 25 3 Metamifop 50 9 100 9 5 1 化合物A-1 10 2 20 4[Test Example 4] (Testing the herbicidal effect by stem and leaf treatment) In a plastic container of 1 /1 0,0 0 acre, the soil of the dry land was planted, and the seed of the grass (Di; Digitaria ciliaris) was seeded. Feed water to the bottom of the container. In the greenhouse, the plated grass (Di) reached the 5-leaf stage. The amount of the hydrating agent prepared in accordance with Example 1 was diluted with water, and the whole plant body was subjected to stem and leaf treatment. Thereafter, it was reared in a glass chamber; after treatment, the herbicidal effect and the degree of phytotoxicity of the day -24-200808182 (20) 3 were expressed as indices on the basis of Table 1. The results are shown in Table 5. The dose is the amount of active ingredient per hectare. Table 5 Herbicides for test herbicide herbicidal effect g ai/ha Di 5 + 25 9 Compound A-1 + Metamifop 10 + 50 10 20 + 100 10 25 3 Metamifop 50 9 100 9 5 1 Compound A-1 10 2 20 4

〔產業上利用性〕 本發明之除草用組成物,係藉由有效成份之選自二氟 甲烷磺醯基替苯胺化合物或其鹽的化合物(成份A)、與 選自特定之除草活性化合物及除草用微生物的至少一種( 成份B)之相乘效果,使除草效果及早顯現、且迅速達成 〇 本發明之除草用組成物,相對於不期望在栽培植物生 育地生長之雜草,具有寬廣之殺草光譜;進而,與既存之 除草劑比較,藥劑處理適用期之寬度廣闊,可長期間抑制 不期望之雜草的生長、且相對於栽培植物不造成藥害,有 助於栽培之省力化與作物之增產。 -25-[Industrial Applicability] The herbicidal composition of the present invention is a compound selected from the group consisting of a difluoromethanesulfonylanilide compound or a salt thereof (ingredient A), and a specific herbicidal active compound and The multiplication effect of at least one of the microorganisms for weeding (component B) allows the herbicidal effect to appear early and quickly achieves the herbicidal composition of the present invention, which is broad relative to the weeds which are not expected to grow in the growing place of the cultivated plants. The herbicidal spectrum; furthermore, compared with the existing herbicides, the pot life of the chemical treatment is wide, and the growth of undesired weeds can be inhibited for a long period of time, and no phytotoxicity is caused relative to the cultivated plants, thereby contributing to the labor saving of cultivation. Increased production with crops. -25-

Claims (1)

200808182 (1) 十、申請專利範圍 1 · 一種除草用組成物,其特徵爲含有: (A)以選自一般式(I)所示之二氟甲烷磺醯基替苯 胺化合物或其鹽之化合物(成份A)、與 • ( B )選自 pyraclonil、imazosulfuron、esprocarb、 % metamifop、triaziflam、pyrazoxyfen、2,4-d、etobenzanid 、mesotrion、tefuryltrione及除草用微生物之至少一種( m 成份b)爲有效成份 R1200808182 (1) X. Patent application scope 1 A herbicidal composition characterized by comprising: (A) a compound selected from the group consisting of a difluoromethanesulfonylanilide compound represented by the general formula (I) or a salt thereof (Component A), and (B) selected from pyraclonil, imazosulfuron, esprocarb, % metamifop, triaziflam, pyrazoxyfen, 2,4-d, etobenzanid, mesotrion, tefuryltrione, and at least one microorganism for weeding (m component b) are effective Ingredient R1 (式中之R1爲氫原子、碳數1〜6之烷基或碳數2〜 6之烷氧基烷基)。 2 ·如申請專利範圍第1項之除草用組成物,其中成份 B 爲 Pyraclonil 〇 3 .如申請專利範圍第1項之除草用組成物,其中成份 B 爲 Tefuryltrione 〇 4.如申請專利範圍第1項之除草用組成物,其中成份 B 爲 Imazo sul fur on 〇 5 .如申請專利範圍第1項之除草用組成物,其中成份 B 爲 Esprocarb 〇 6.如申請專利範圍第1項之除草用組成物,其中成份 B 爲 Metamifop -26- 200808182 (2) 7 ·如申請專利範圍第1項之除草用組成物,其中成份 B 爲 Triaziflam 〇 8 ·如申請專利範圍第1項之除草用組成物,其中成份 B 爲 Pyrazoxyfen ° ^ 9 ·如申請專利範圍第1項之除草用組成物,其中成份 • B 爲 2,4-D。 1 0 .如申請專利範圍第1項之除草用組成物,其中成 份 B 爲 Etobenzanid。 1 1 ·如申請專利範圍第1項之除草用組成物,其中成 份 B 爲 Mesotrion。 1 2 ·如申請專利範圍第1項之除草用組成物,其中成 份B爲除草用微生物。 1 3 ·如申請專利範圍第1 2項之除草用組成物,其中除 草用微生物爲 Drechslera monoceras,MTB-951 株。 1 4 .如申請專利範圍第1項之除草用組成物,其中相 φ 對於成份A之1質量份,以0.1〜2,000質量份之範圍配 合成份B。 1 5 . —種抑制栽培植物中所不期望雜草之成長的方法 ,其特徵爲將除草有效量之如申請專利範圍第1〜13項中 任一項之除草用組成物,對使栽培植物生長或栽培植物生 長之處所作用。 1 6 ·如申請專利範圍第1 5項之方法’其係將除草用組 成物作成粉劑、微粒劑或粒劑,以成份A與成份B之合 計量計,每10公畝爲0.1 g〜5kg之範圍施用。 -27- 200808182 ⑶ 17·如申請專利範圍第15項之方法,其係將除草用組 成物調成乳劑、液劑、可流動劑或水合劑,在成份Α與 成份B之合計濃度爲1〇〜i〇〇,〇〇〇ppm之範圍施用。 18·如申請專利範圍第15項之方法,其中栽培植物爲 m 水田作物、旱地作物、園藝作物、矮草、果樹、非農耕地 # 栽培植物。 19·如申請專利範圍第15項之方法,其中使栽培植物 • 生長或生長之處所爲水田、旱地、矮草地或非農耕地。 -28- 200808182 f 無 • · 明 說 單 無簡 JLIU :# 為符 圖件 表元 代之 定圖 :指表 圖案代 表本本 ^ Nly ) 定一二 指CC 七 八、本案若有化學式時,請揭示最能顯示發明特徵的化學 式:式(I ) R1(wherein R1 is a hydrogen atom, an alkyl group having 1 to 6 carbon atoms or an alkoxyalkyl group having 2 to 6 carbon atoms). 2) The herbicidal composition of claim 1 wherein the component B is Pyraclonil 〇3. The herbicidal composition of claim 1 is wherein the component B is Tefuryltrione 〇 4. as claimed in claim 1 The herbicidal composition of the present invention, wherein the component B is Imazo sul fur on 〇5. The herbicidal composition of claim 1 wherein the component B is Esprocarb 〇 6. The composition for weeding according to claim 1 The component B is Metamifop -26- 200808182 (2) 7 · The herbicidal composition according to claim 1 of the patent scope, wherein the component B is Triaziflam 〇8 · The herbicidal composition according to claim 1 of the patent scope, The component B is Pyrazoxyfen ° ^ 9 · The herbicidal composition of claim 1 of the patent scope, wherein the component B is 2,4-D. 1 0. For the herbicidal composition of claim 1, the component B is Etobenzanid. 1 1 · For the herbicidal composition of claim 1, the component B is Mesotrion. 1 2 . The herbicidal composition of claim 1, wherein component B is a microorganism for weeding. 1 3 · The herbicidal composition of claim 12, wherein the microorganism for weeding is Drechslera monoceras, MTB-951 strain. In the herbicidal composition of claim 1, wherein the phase φ is 1 part by mass of the component A, the component B is compounded in an amount of 0.1 to 2,000 parts by mass. A method for inhibiting the growth of undesirable weeds in a cultivated plant, characterized in that the herbicidal effective amount of the herbicidal composition according to any one of claims 1 to 13 is applied to the cultivated plant. The role of growing or growing plants. 1 6 · The method of claim 15 of the patent application 'the method for making the herbicidal composition into a powder, a microparticle or a granule, and the total amount of the component A and the component B is 0.1 g to 5 kg per 10 ares. The scope of application. -27- 200808182 (3) 17. The method of claim 15 is to adjust the herbicidal composition into an emulsion, a liquid, a flowable agent or a hydrating agent, and the total concentration of the component Α and the component B is 1〇. ~i〇〇, 〇〇〇ppm range of application. 18. The method of claim 15, wherein the cultivated plants are m paddy crops, dry land crops, horticultural crops, dwarf grasses, fruit trees, non-agricultural land #cultivated plants. 19. The method of claim 15, wherein the cultivated plant is grown or grown in a paddy field, a dry land, a dwarf grassland or a non-agricultural land. -28- 200808182 f 无• · Ming said that there is no simple JLIU: # is the map of the map element on behalf of the map: refers to the table pattern represents the book ^ Nly) fixed one or two refers to CC seven eight, if the case has a chemical formula, please reveal The chemical formula that best shows the characteristics of the invention: Formula (I) R1 nhso2chf2 n=&lt;0CH3 \〇CH3 (I)Nhso2chf2 n=&lt;0CH3 \〇CH3 (I)
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* Cited by examiner, † Cited by third party
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CN102480947A (en) * 2009-05-27 2012-05-30 拜尔农作物科学股份公司 Herbicide combinations comprising tefuryltrione for use in rice cultures

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CN101778565B (en) * 2007-08-10 2014-10-15 组合化学工业株式会社 Composition for weeding
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IN2014CH00327A (en) * 2014-01-27 2015-08-14 Mr Praharaju Laxminarayana
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* Cited by examiner, † Cited by third party
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DE19521355A1 (en) * 1995-06-12 1996-12-19 Hoechst Schering Agrevo Gmbh Sulfonamides, processes for their preparation and their use as herbicides and plant growth regulators
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JP2004292417A (en) * 2003-03-26 2004-10-21 Sds Biotech:Kk Phytotoxicity reducing and weeding method
JP2006056870A (en) * 2004-04-01 2006-03-02 Bayer Cropscience Ag Difluoromethanesulfonamide derivative and herbicide
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CN102480947A (en) * 2009-05-27 2012-05-30 拜尔农作物科学股份公司 Herbicide combinations comprising tefuryltrione for use in rice cultures
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