WO2007018160A1 - Aqueous suspension-type herbicide composition - Google Patents

Aqueous suspension-type herbicide composition Download PDF

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Publication number
WO2007018160A1
WO2007018160A1 PCT/JP2006/315531 JP2006315531W WO2007018160A1 WO 2007018160 A1 WO2007018160 A1 WO 2007018160A1 JP 2006315531 W JP2006315531 W JP 2006315531W WO 2007018160 A1 WO2007018160 A1 WO 2007018160A1
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WO
WIPO (PCT)
Prior art keywords
aqueous suspension
herbicidal composition
weight
parts
sulfonate
Prior art date
Application number
PCT/JP2006/315531
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French (fr)
Japanese (ja)
Inventor
Yoshiaki Ishihara
Tatsuhiko Tsuruta
Original Assignee
Ishihara Sangyo Kaisha, Ltd.
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Ishihara Sangyo Kaisha, Ltd. filed Critical Ishihara Sangyo Kaisha, Ltd.
Priority to CN2006800286676A priority Critical patent/CN101237770B/en
Priority to KR1020087003231A priority patent/KR101246484B1/en
Publication of WO2007018160A1 publication Critical patent/WO2007018160A1/en

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Classifications

    • 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
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/02Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
    • A01N25/04Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
    • 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
    • A01N47/28Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/36Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues 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
    • 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
    • A01N47/28Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/38Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof

Definitions

  • the present invention relates to an aqueous suspension herbicidal composition in which the herbicidal sulfo-urea compound or a salt thereof is inhibited from being decomposed in water and stable suspension is maintained.
  • herbicides have been developed and put to practical use for the purpose of crop protection in cultivated land and weed control in non-agricultural land.
  • these herbicides are applied in the form of solid powders, granules, and other solid preparations that are sprayed by diluting in water at the time of use, such as power wettable powders and granular wettable powders.
  • it may be a liquid suspension formulation in which an active ingredient is suspended in water, vegetable oil, etc., together with a surfactant, etc. and diluted with water at the time of use.
  • a liquid suspension formulation is desirable to avoid.
  • the scale on the drug product bottle can be easily adjusted.
  • the liquid preparation that can be used is more advantageous than the solid preparation that requires a weighing machine such as a balance to measure the weight.
  • those suspended in vegetable oil are often used for cultivated cereals.
  • the organic solvent used in the emulsion is preferably not used as much as possible from the viewpoint of the effect on the surrounding environment to be applied or the flammability of the preparation, or even if used, the amount is preferably as small as possible. It is desired to prepare an aqueous suspension herbicidal composition that is stably suspended in water!
  • a sulfonylurea compound as a compound blended as an active ingredient of a herbicide is a compound that exhibits an excellent herbicidal effect at a relatively small application amount, and is therefore used as an active ingredient in many herbicides.
  • sulfo-urea compounds or their salts formulated as herbicidal active ingredients generally have a property that they are easily decomposed during storage. If the active ingredient concentration in the formulation decreases due to their decomposition, the herbicidal effect expected at the time of application cannot be exhibited, or the internal pressure of the suspension storage container is stored due to gas generation due to decomposition. May be high inside. As a result, the suspension liquid blows out at the time of opening, and the contents may cause various inconveniences such as contamination of workers and surroundings.
  • Japanese Patent Application Laid-Open No. 2000-159603 discloses an aqueous suspension herbicidal composition containing a herbicidal sulfo-lurea compound and phenol sulfonate or a formalin condensate thereof.
  • JP-A-59-205305 discloses an aqueous suspension herbicidal composition
  • a herbicidal sulfo-urea compound salt and an ammonium or alkali metal salt of a carboxylic acid or inorganic acid. It is disclosed. Specifically, at the time of producing the aqueous suspension herbicidal composition, the herbicidal sulfonylurea compound and the surfactant are mixed in water, and then added to the carboxylic acid or inorganic acid ammonium salt or alkali.
  • Patent No. 3,175,850 discloses preparing an aqueous suspension preparation of pyrazosulfuron using an inorganic acid, an organic acid or a buffer.
  • Patent Document 1 JP 2000-159603 A
  • Patent Document 2 JP 59-205305 A
  • Patent Document 3 Japanese Patent No. 3,175,850
  • the herbicidal sulfonylurea compound which is an active ingredient used in the present invention, is easily decomposed in water or produced as a suspension thereof. Since the process is complicated, practical examples have been seldom seen. Therefore, it is desired to prepare an aqueous suspension herbicidal composition that does not decompose a herbicidal sulfonylurea compound in water and maintains a stable suspended state without going through complicated steps.
  • the present inventors have conducted various studies to solve the above problems. As a result, by using an inorganic salt and a sulfonate salt as a specific surfactant, the herbicidal sulfo-urea compound does not decompose in water and maintains an aqueous suspension herb. The present inventors have found that the composition can be prepared without going through complicated steps and completed the present invention.
  • the present invention relates to (1) 1- [3-— [(4,6 dimethoxypyrimidine-2-ylcarbamoyl) sulfamoyl] -2-pyridyl] -2-fluoropropyl methoxyacetate, N-[(4, 6 dimethoxypyrimidine 2-yl) aminocarbol] — 2— (2 fluoro 1-hydroxypropyl) — 3-pyridinesulfonamides and their salt strength group power at least one herbicidal sulfonyl selected Urea compounds, (2) inorganic salts, (3) at least one sulfonate selected from the group consisting of aryl sulfonates, alkyl aryl sulfonates and their formalin condensates, and (4)
  • the present invention relates to an aqueous suspension herbicidal composition containing water, and a method for controlling undesired plants or suppressing the growth thereof using the composition.
  • the present invention provides an aqueous solution using an inorganic salt and an arylene sulfonate, an alkylaryl sulfonate, and at least one sulfonic acid salt selected from the group strength of their formalin condensate.
  • the present invention provides at least (1) 1- [3-[(4,6 dimethoxypyrimidine-2-ylcarbamoyl) sulfamoyl] -2-pyridyl] -2-fluoropropyl methoxyacetate , N- [(4, 6 dimethoxypyrimidine 1-2-yl) aminocarbol] — 2— (2 fluoro — 1 hydroxypropyl) 1 3 pyridinesulfonamide and at least one selected from the group consisting of their salt strength At least one sulfonic acid selected from the group consisting of (2) inorganic salts, (3) aryl sulfonates, alkyl aryl sulfonates and their formalin condensates
  • the present invention relates to a method for producing an aqueous suspension herbicidal composition by mixing a salt and (4) water and, if desired, wet milling.
  • an aqueous suspension herbicide in which the decomposition of the herbicidal sulfonylurea compound or a salt thereof is suppressed in the aqueous suspension herbicidal composition and the suspension of the preparation is sufficiently maintained.
  • a composition and a herbicidal method using the composition can be provided.
  • an aqueous suspension herbicidal composition can be prepared by mixing each component of the preparation and optionally wet-grinding, so that the active ingredient is once dissolved and reprecipitated. No manufacturing process is required.
  • the herbicidal sulfo-lurea compound used in the present invention is 1 [3— [(4,6-Dimethyoxypyrimidine-2-ylcarbamoyl) sulfamoyl] -2-cyclopyridyl] -2-fluoropropyl.
  • It is an amide (hereinafter referred to as Compound A2) or a salt thereof.
  • the salt include various salts. For example, salts with alkali metals such as sodium and potassium; salts with alkaline earth metals such as magnesium and calcium; salts with amines such as monomethylamine, dimethylamine and triethylamine.
  • Various inorganic salts are used in the present invention.
  • alkali metal phosphates and alkaline earth metal phosphates are used in the present invention.
  • alkali metal phosphates are desirable, and among these, sodium dihydrogen phosphate and potassium dihydrogen phosphate are more desirable.
  • the alkyl moiety in the sulfonates used in the present invention may be a linear one. However, it may be branched. Examples thereof include those having C to c such as methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl and the like.
  • Examples of the aryl moiety in the sulfonates include monocyclic or polycyclic compounds such as a benzene ring or a naphthalene ring.
  • Examples of the sulfonate salts include various salts. Examples include salts with alkali metals such as sodium and potassium; salts with alkaline earth metals such as magnesium and calcium.
  • the sulfonates are preferably alkylaryl sulfonates or formalin condensates thereof, more preferably alkylbenzene sulfonates, alkyl naphthalene sulfonates, alkylbenzene sulfonate formalin condensates, It is an alkyl naphthalene sulfonate formalin condensate.
  • alkylbenzene sulfonate formalin condensate and alkyl naphthalene sulfonate formalin condensate are more desirable.
  • the aqueous suspension herbicidal composition of the present invention may contain various adjuvants as desired.
  • Various adjuvants may be used as long as they are used in the technical field.
  • Specific examples of these various adjuvants include the following.
  • the preparation of the preparation can be performed according to a usual method in the technical field.
  • surfactants include, for example, fatty acid salts, benzoates, alkylsulfosuccinates, dialkylsulfosuccinates, polycarboxylates, alkyl sulfate esters, alkyl sulfates, alkyl diglycol ether sulfates.
  • anti-settling agent examples include silica, organic bentonite (Bentonite-alkylamino complex), bentonite, white carbon, and aluminum magnesium caustic acid. If desired, two or more of these may be mixed as appropriate.
  • thickener examples include heteropolysaccharides such as xanthan gum and guar gum; water-soluble polymers such as polybulal alcohol, sodium carboxymethylcellulose and sodium alginate; bentonite and white carbon. If desired, two or more of these may be mixed as appropriate.
  • antifoaming agent examples include polydimethylsiloxane and acetylene alcohol. If desired, two or more of these may be mixed as appropriate.
  • antifreezing agent examples include ethylene glycol, propylene glycol, glycerin, urea and the like. If desired, two or more of these may be mixed as appropriate.
  • preservatives examples include formalin, parachlorometaxylenol, 1,2-benzisothia Zolin-3-one and the like. If desired, two or more of these may be mixed as appropriate.
  • the solvent examples include monohydric alcohols such as propanol and isobutanol; polyhydric alcohols such as ethylene glycol, propylene glycol, diethylene glycol, hexylene glycol, polyethylene glycol, polypropylene glycol, and glycerin; propyl Such as cellosolve, butylcerosolve, ferrulecetosolve, propylene glycol monomethino ethenore, propylene glycol monomethino enoate, propylene glycol monopropyl ether, propylene glycol monobutyl ether, propylene glycol monophenol ether Glycol ethers; Ethers such as dioxane; Ketones such as cyclohexanone and methyl isobutyl ketone; Fatty acids such as acetic acid and butyric acid Esters such as isopropyl acetate and butyl acetate; nitrogen-containing sulfur-containing solvents such as N-
  • herbicidal compounds other than the herbicidal sulfonylurea compound or a salt thereof can be mixed or used together, and in this case, a further excellent effect, May exhibit activity.
  • the range of applicable grass species, the timing of chemical treatment, herbicidal activity, etc. may be improved in the preferred direction.
  • the herbicidal sulfo-lurea compound or its salt and other herbicidal compounds may be used separately in the form of a mixture prepared at the time of spraying. Use it as a turbid mixed herbicidal composition.
  • the present invention includes the above-described aqueous suspension mixed herbicidal composition and a method for controlling undesired plants or suppressing the growth thereof using the composition.
  • the present invention also includes a method for controlling undesired plants or suppressing the growth thereof by using separately prepared herbicidal sulfonylurea compounds or salts thereof and other herbicidal compounds. included.
  • herbicidal compounds can be selected as appropriate from, for example, the following compound groups (1) to (11) (generic names; some including those in the application for ISO). Even if there is no specific description, this When these compounds contain various structural isomers such as salts, alkyl esters and optical isomers, they are naturally included.
  • a quaternary ammonia such as paraquat or diquat, which is said to be a free radical in the plant itself, generating active oxygen and exhibiting rapid herbicidal efficacy. Salt system.
  • Uron imazosulfuron (imazosulfuron), cyclosulfamuron (cyclosulfamuron), prosulforon (prosulforon), flupirsulfuron (flupyrsulluron), triflusulfuron-methyl (triflusulforon-methyl), Halosulforon-methyl, thifensulforon- methyl), ethoxysulforon, oxasulforon, ethametsulfuron, iodosnorephron uodosulfuron, snolefosnoreflon sulfosulfuron, triasulforon, tribenuron methyl (tribenuron methyl) , Tritosulforon, foramsulforon, tri floxysulluron, isosulforon-methyl, mesosulfuron-methyl, talent noresosno Sulfo-Rule
  • Di-troaline systems such as trifluralin, oryzalin, oritalin, nitraline, pendimethalin, ethalfluralin, benfluralin, prodiamine Amides such as bensulide, napronamide, pronamide; amiprofos-methyl, butamifos, alofos, hyperophos, Organophosphorus such as piperophos; phelocarbamates such as propham, chlorpropham, and barban; daimuron, cumyluron, bromobutide Cumylamines such as asuram, dithiopyr, thiazopyr, cafenst role), indanofan, etc., which are said to show herbicidal efficacy by inhibiting cell mitosis in plants.
  • Di-troaline systems such as trifluralin, oryzalin, oritalin, nitraline, pendimethalin, ethalfluralin, benfluralin, pro
  • herbicidal efficacy by inhibiting plant protein biosynthesis or lipid biosynthesis.
  • EPTC butylate, vernolate, pebulate, cycloate, prosulfocarb, esprocarb, thiobencarb, dialate Thiocarbamates such as diallate and triallate; MSMA, DSMA, endothal, etho! Umesate, sodium chlorate, befrugonic acid ), Fosamine, pinoxaden, HOK-201 and the like.
  • the blending ratio of each component in the aqueous suspension herbicidal composition of the present invention cannot be specified unconditionally because it may be changed as appropriate according to the type of the blending component, the formulation form, the application scene, and the like.
  • Compound Al, Compound A 2 or a salt thereof as a herbicidal sulfonylurea compound is 0.1 to 60 parts by weight, preferably 0.5 to 50 parts by weight, and an inorganic salt is 0.1 to 25 parts by weight, preferably 1 to 20 parts by weight, more preferably 2 to 10 parts by weight, sulfonates are 0.01 to 30 parts by weight, preferably 0.1 to 20 parts by weight, and the remaining main component is water.
  • 0.01 to 10 parts by weight, preferably 0.05 to 5 parts by weight when blending thickeners 0.001 to 10 parts by weight, desirably 0.01 to 5 parts by weight when blending antifoaming agents 0.01 to 10 parts by weight, preferably 0.05 to 5 parts by weight when preservatives are added, 1 to 70 parts by weight, preferably 1 to 50 parts by weight, etc.
  • the herbicidal compound When the herbicidal compound is added, it is 0.1 to 60 parts by weight, preferably 0.1 to 50 parts by weight.
  • the aqueous suspension herbicidal composition of the present invention is applied to an undesired plant or a place where it grows, and is treated with, for example, a foliage treatment, a soil treatment, or a flooding treatment to produce annual weeds or perennials.
  • a foliage treatment for example, a foliage treatment, a soil treatment, or a flooding treatment to produce annual weeds or perennials.
  • a wide range of harmful plants such as weeds can be controlled or their growth can be suppressed.
  • Examples of harmful plants include Inubie, Tainubie, Barefoot, Enokorogusa, Akinoenokorogosa, Ohashiba, Oats, Oats, Sowbill, Cypress, Velvet Millet, Paragrass, Azegaya, Itasegaya, Sparrows Mosquitoes, fireflies, staghorns, moths, crabs and weeds; Of Camiaceae; Ichibi, Maruba morning glory, white-tailed, American goldfish, Suberuhi, Aobu, Aguayte, Yebisuda, Inho Examples include zuki bean, sanaetade, chickweed, onamomi, tanekikebana, photokenosa, ragweed, yaemdara, hinoki hinagao, datura, ezonokine thisami, and enoki tasa.
  • Herbicidal Compound Al, Compound A2 or a salt thereof as a sulfo-lurea compound can be applied at a rate of 1 to 500 g, preferably 2 to 250 g per lha.
  • Example 1 The ability to describe examples of the present invention below The present invention is not limited to these.
  • Example 1 The ability to describe examples of the present invention below The present invention is not limited to these.
  • Example 2 An aqueous suspension herbicidal composition was obtained by mixing the above ingredients and pulverizing with a wet pulverizer for 5 minutes.
  • Example 3 Aqueous suspension herbicidal composition was prepared by mixing 10.0 parts by weight or more of water containing 1,2-benzisothiazolin-3-one (1.0 part by weight) and then wet-grinding it with a wet grinder for 5 minutes.
  • Rhodorsil 432 (same as above) 0.1 parts by weight
  • Rhodorsil 432 (same as above) 0.1 parts by weight
  • Example 5 The above ingredients were mixed and pulverized with a wet pulverizer for 5 minutes to obtain an aqueous suspension herbicidal composition. [0046] Example 5
  • the above ingredients were mixed and pulverized with a wet pulverizer for 5 minutes to obtain an aqueous suspension herbicidal composition.
  • Rhodorsil 432 (same as above) 0.1 parts by weight
  • Rhodorsil 432 (same as above) 0.1 parts by weight
  • the above ingredients were mixed and pulverized with a wet pulverizer for 5 minutes to obtain an aqueous suspension herbicidal composition.
  • Example 1 The aqueous suspension herbicidal compositions of Example 1 and Comparative Example 1 were stored in a thermostat at 54 ° C. for 14 days.
  • Decomposition rate (%) [(Content immediately after production Content after storage) Z Content immediately after production] X 1 00
  • aqueous suspension of the present invention A predetermined amount (100 g ai / ha) of a herbicidal composition is diluted with water equivalent to 300 L / ha, and a spreading agent (trade name: Surfatatanto WK, manufactured by Kao Corporation) is added here. , Handle the foliage. On the 21st day after treatment, investigate the growth of the plant. As a result, the aqueous suspension herbicidal composition of the present invention exhibits excellent herbicidal activity.
  • the aqueous suspension herbicidal composition of the present invention is effectively used for crop protection in cultivated land and weed control in non-agricultural land.
  • the Japanese Patent Application 2005- 231841 filed on August 10, 2005 the Japanese Patent Application 2005-326624 filed on November 10, 2005, and the February 21, 2006 application
  • the entire contents of the specification, claims, and summary of Japanese Patent Application No. 2006-044472 are incorporated herein by reference as the disclosure of the specification of the present invention.

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Dentistry (AREA)
  • Plant Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Wood Science & Technology (AREA)
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Abstract

The object is to prepare an aqueous suspension-type herbicide composition which can avoid the decomposition of a herbicidal sulfonylurea compound in water and can also retain a stable suspension state, without the need of using any complicated step. An aqueous suspension-type herbicide composition comprising: (1) at least one herbicidal sulfonylurea compound selected from the group consisting of 1-[3-[(4,6-dimethoxypyrimidin- 2-ylcarbamoyl)sulfamoyl]-2-pyridyl]-2-fluoropropyl methoxyacetate, N-[(4,6-dimethoxypyrimidin-2- yl)aminocarbonyl]-2-(2-fluoro-1-hydroxypropyl)-3- pyridinesulfonamide and salts thereof; (2) an inorganic salt; (3) at least one sulfonate salt selected from the group consisting of an arylsulfonate, an alkylarylsulfonate and formalin condensates thereof; and (4) water.

Description

明 細 書  Specification
水性懸濁状除草組成物  Aqueous suspension herbicidal composition
技術分野  Technical field
[0001] 本発明は、除草性スルホ -ルゥレア系化合物又はその塩の水中での分解が抑制さ れ且つ安定な懸濁性が保たれる水性懸濁状除草組成物に関する。  [0001] The present invention relates to an aqueous suspension herbicidal composition in which the herbicidal sulfo-urea compound or a salt thereof is inhibited from being decomposed in water and stable suspension is maintained.
背景技術  Background art
[0002] これまで、耕作地における作物保護や非農耕地での雑草防除の目的で様々な除 草剤が開発、実用化されている。一般にこれら除草剤の施用形態は、粉剤、粒剤な どの固形物を直接散布する製剤である力 水和剤や顆粒水和剤などのように使用時 に水に希釈して散布する固形の製剤であるか、或いは有効成分を水、植物油などに 界面活性剤などとともに懸濁させた製剤を使用時に水で希釈して散布するような液 体の懸濁製剤であったりする。  [0002] So far, various herbicides have been developed and put to practical use for the purpose of crop protection in cultivated land and weed control in non-agricultural land. In general, these herbicides are applied in the form of solid powders, granules, and other solid preparations that are sprayed by diluting in water at the time of use, such as power wettable powders and granular wettable powders. Alternatively, it may be a liquid suspension formulation in which an active ingredient is suspended in water, vegetable oil, etc., together with a surfactant, etc. and diluted with water at the time of use.
[0003] これらのうち、固形物を直接散布する製剤や水に希釈して使用する固形の製剤を 取り扱う際、使用の際に空中に舞い上がった固形物を使用者が吸い込む場合があり 、これを避ける為には液体の懸濁製剤が望ましい。さら〖こ、散布対象の面積が製剤 1 包装あたりの面積と異なるなどの理由で、製剤品の量を簡単に計量して加減するた めには、製剤ボトルに備え付けられた目盛りなどを容易に使用できる液体製剤は、重 量を計測するために天秤のような計量機などを用意しなけばならない固形製剤よりも 、有利である。また、液体の懸濁製剤のうち、植物油に懸濁させた製剤は、穀物の耕 作地に対して使用されることが多い。しかし、道路、線路、工場の敷地、運動場など の非農耕地や、果樹園、桑畑などに対し、植物油に懸濁させた製剤を使用した場合 、散布後、植物油成分が地面に一時残るため、散布後、当該場所を利用する際に不 便な場合がある。更に、乳剤などに使用される有機溶媒などは、施用する周辺環境 への影響或いは製剤の引火性などの観点から、できるだけ使用しないか、使用する 場合でもその量は極力少な 、ほうが好ましく、有効成分を安定して水に懸濁させた水 性懸濁状除草組成物を調製することが望まれて!/ヽる。  [0003] Among these, when handling a preparation directly spraying solids or a solid preparation used by diluting in water, the user may inhale the solids that have risen into the air during use. A liquid suspension formulation is desirable to avoid. In order to easily measure and adjust the amount of drug product because the area to be sprayed is different from the area per package of the drug product, the scale on the drug product bottle can be easily adjusted. The liquid preparation that can be used is more advantageous than the solid preparation that requires a weighing machine such as a balance to measure the weight. Of the liquid suspension formulations, those suspended in vegetable oil are often used for cultivated cereals. However, when a formulation suspended in vegetable oil is used on non-agricultural land such as roads, railways, factory grounds, playgrounds, orchards, and mulberry fields, vegetable oil components remain on the ground after spraying. It may be inconvenient to use the site after spraying. Furthermore, the organic solvent used in the emulsion is preferably not used as much as possible from the viewpoint of the effect on the surrounding environment to be applied or the flammability of the preparation, or even if used, the amount is preferably as small as possible. It is desired to prepare an aqueous suspension herbicidal composition that is stably suspended in water!
[0004] 一方、除草剤の有効成分として配合される化合物としてスルホニルゥレア系化合物 又はその塩は、施用量が比較的少量で優れた除草効果を発揮する化合物であるこ とから、数多くの除草剤の有効成分として利用されている。しかし、除草有効成分とし て配合されるスルホ -ルゥレア系化合物又はその塩は、一般に保存中に分解しやす い性質を持っている。それらの分解により、製剤中の有効成分濃度が低下すると、施 用の際に期待される除草効果が発揮できなくなったり、分解によるガスの発生によつ て懸濁液の保存容器の内圧が保管中に高くなることがある。それにより開封時に懸 濁液が吹き出て、内容物が作業者や周辺を汚染するなど様々な不都合を惹起する 場合がある。 [0004] On the other hand, a sulfonylurea compound as a compound blended as an active ingredient of a herbicide Alternatively, the salt is a compound that exhibits an excellent herbicidal effect at a relatively small application amount, and is therefore used as an active ingredient in many herbicides. However, sulfo-urea compounds or their salts formulated as herbicidal active ingredients generally have a property that they are easily decomposed during storage. If the active ingredient concentration in the formulation decreases due to their decomposition, the herbicidal effect expected at the time of application cannot be exhibited, or the internal pressure of the suspension storage container is stored due to gas generation due to decomposition. May be high inside. As a result, the suspension liquid blows out at the time of opening, and the contents may cause various inconveniences such as contamination of workers and surroundings.
[0005] これまでに、除草有効成分として配合されるスルホニルゥレア系化合物又はその塩 の分解を防止する為、様々な化合物を添加することが検討されてきた。例えば、特開 2000-159603では、除草性スルホ -ルゥレア系化合物とフエノールスルホン酸塩又は そのホルマリン縮合物とを配合した水性懸濁状除草組成物が開示されている。  [0005] So far, it has been studied to add various compounds in order to prevent decomposition of the sulfonylurea compound or its salt blended as an active herbicidal ingredient. For example, Japanese Patent Application Laid-Open No. 2000-159603 discloses an aqueous suspension herbicidal composition containing a herbicidal sulfo-lurea compound and phenol sulfonate or a formalin condensate thereof.
[0006] また、特開昭 59-205305では、除草性スルホ -ルゥレア系化合物の塩と、カルボン 酸又は無機酸のアンモ-ゥム又はアルカリ金属塩とを配合した水性懸濁状除草組成 物が開示されている。具体的には、当該水性懸濁状除草組成物の製造時、除草性 スルホニルゥレア系化合物と界面活性剤を水中で混合後、そこへカルボン酸又は無 機酸のアンモ-ゥム塩又はアルカリ金属塩を投入することで、除草性スルホニルウレ ァ系化合物の塩を形成させて沈殿させ、沈殿した除草性スルホニルゥレア系化合物 の塩を湿式粉砕機などによって水中で分散させることが開示されている。  [0006] JP-A-59-205305 discloses an aqueous suspension herbicidal composition comprising a herbicidal sulfo-urea compound salt and an ammonium or alkali metal salt of a carboxylic acid or inorganic acid. It is disclosed. Specifically, at the time of producing the aqueous suspension herbicidal composition, the herbicidal sulfonylurea compound and the surfactant are mixed in water, and then added to the carboxylic acid or inorganic acid ammonium salt or alkali. It is disclosed that by adding a metal salt, a herbicidal sulfonylurea compound salt is formed and precipitated, and the precipitated herbicidal sulfonylurea compound salt is dispersed in water by a wet pulverizer or the like. Yes.
[0007] 更に、特許第 3, 175,850号では、無機酸、有機酸又は緩衝液を用いてピラゾスルフ ロンの水性懸濁製剤を調製することが開示されている。  [0007] Further, Patent No. 3,175,850 discloses preparing an aqueous suspension preparation of pyrazosulfuron using an inorganic acid, an organic acid or a buffer.
[0008] 特許文献 1:特開 2000-159603号公報  [0008] Patent Document 1: JP 2000-159603 A
特許文献 2:特開昭 59-205305号公報  Patent Document 2: JP 59-205305 A
特許文献 3:特許第 3, 175,850号公報  Patent Document 3: Japanese Patent No. 3,175,850
発明の開示  Disclosure of the invention
発明が解決しょうとする課題  Problems to be solved by the invention
[0009] 前述の従来技術を適用した場合であっても、本発明に使用する有効成分である除 草性スルホニルゥレア系化合物は、水中で分解しやすい或いはその懸濁液の製造 工程が煩雑である為、実用化された例はあまり見られな力つた。従って、除草性スル ホニルゥレア系化合物が水中で分解せず、且つ安定な懸濁状態を保つ水性懸濁状 除草組成物を、煩雑な工程を経ることなく調製することが希求されて ヽる。 [0009] Even when the above-described prior art is applied, the herbicidal sulfonylurea compound, which is an active ingredient used in the present invention, is easily decomposed in water or produced as a suspension thereof. Since the process is complicated, practical examples have been seldom seen. Therefore, it is desired to prepare an aqueous suspension herbicidal composition that does not decompose a herbicidal sulfonylurea compound in water and maintains a stable suspended state without going through complicated steps.
課題を解決するための手段  Means for solving the problem
[0010] 本発明者らは、上記課題を解決するべぐ種々検討を行なった。その結果、無機塩 と特定の界面活性剤であるスルホン酸塩類とを使用することにより、除草性スルホ- ルゥレア系化合物が水中で分解せず、且つ安定な懸濁状態を保つ水性懸濁状除草 組成物を煩雑な工程を経ることなく調製することができることを見出し、本発明を完成 した。  [0010] The present inventors have conducted various studies to solve the above problems. As a result, by using an inorganic salt and a sulfonate salt as a specific surfactant, the herbicidal sulfo-urea compound does not decompose in water and maintains an aqueous suspension herb. The present inventors have found that the composition can be prepared without going through complicated steps and completed the present invention.
[0011] 即ち、本発明は、(1) 1— [3— [ (4,6 ジメトキシピリミジン一 2—ィルカルバモイル) スルファモイル] - 2-ピリジル] - 2-フルォロプロピル メトキシアセテート、 N— [ (4 , 6 ジメトキシピリミジン一 2—ィル)ァミノカルボ-ル]— 2— (2 フルォロ一 1—ヒド ロキシプロピル)— 3—ピリジンスルホンアミド及びそれらの塩力 なる群力 選ばれた 少なくとも 1種の除草性スルホニルゥレア系化合物、(2)無機塩、(3)ァリールスルホ ン酸塩、アルキルァリールスルホン酸塩及びそれらのホルマリン縮合物からなる群か ら選ばれた少なくとも 1種のスルホン酸塩並びに (4)水を含有する水性懸濁状除草 組成物、並びに該組成物を用いて望ましくない植物を防除又はその生育を抑制する 方法に関する。  [0011] That is, the present invention relates to (1) 1- [3-— [(4,6 dimethoxypyrimidine-2-ylcarbamoyl) sulfamoyl] -2-pyridyl] -2-fluoropropyl methoxyacetate, N-[(4, 6 dimethoxypyrimidine 2-yl) aminocarbol] — 2— (2 fluoro 1-hydroxypropyl) — 3-pyridinesulfonamides and their salt strength group power at least one herbicidal sulfonyl selected Urea compounds, (2) inorganic salts, (3) at least one sulfonate selected from the group consisting of aryl sulfonates, alkyl aryl sulfonates and their formalin condensates, and (4) The present invention relates to an aqueous suspension herbicidal composition containing water, and a method for controlling undesired plants or suppressing the growth thereof using the composition.
[0012] また、本発明は、無機塩と、ァリールスルホン酸塩、アルキルァリールスルホン酸塩 及びそれらのホルマリン縮合物力 なる群力 選ばれた少なくとも 1種のスルホン酸 塩とを用いて、水性懸濁状除草組成物中の 1 [3— [ (4,6 ジメトキシピリミジン— 2 —ィルカルバモイル)スルファモイル]— 2—ピリジル]— 2—フルォロプロピルメトキシ アセテート、 N— [ (4, 6 ジメトキシピリミジン一 2—ィル)ァミノカルボ-ル]— 2— (2 フルォロ 1 ヒドロキシプロピル) 3 ピリジンスルホンアミド及びそれらの塩か らなる群カゝら選ばれた少なくとも 1種の除草性スルホニルゥレア系化合物を安定ィ匕さ せる方法に関する。  [0012] Further, the present invention provides an aqueous solution using an inorganic salt and an arylene sulfonate, an alkylaryl sulfonate, and at least one sulfonic acid salt selected from the group strength of their formalin condensate. 1 [3— [(4,6 Dimethoxypyrimidine—2-ylcarbamoyl) sulfamoyl] — 2-pyridyl] —2-fluoropropylmethoxyacetate, N— [(4,6 dimethoxy) in suspension herbicidal composition Pyrimidine 2-yl) aminocarbol] — 2-— (2 fluoro 1 hydroxypropyl) 3 At least one herbicidal sulfonylurea compound selected from the group consisting of pyridinesulfonamide and salts thereof. It is related with the method of stabilizing.
[0013] 更に、本発明は、少なくとも(1) 1— [3— [ (4,6 ジメトキシピリミジン— 2—ィルカル バモイル)スルファモイル]— 2—ピリジル]— 2—フルォロプロピル メトキシアセテート 、 N-[ (4, 6 ジメトキシピリミジン一 2—ィル)ァミノカルボ-ル]— 2— (2 フルォロ — 1 ヒドロキシプロピル)一 3 ピリジンスルホンアミド及びそれらの塩力 なる群から 選ばれた少なくとも 1種の除草性スルホ -ルゥレア系化合物、(2)無機塩、(3)ァリー ルスルホン酸塩、アルキルァリールスルホン酸塩及びそれらのホルマリン縮合物から なる群カゝら選ばれた少なくとも 1種のスルホン酸塩並びに (4)水を混合し、所望により 湿式粉砕して水性懸濁状除草組成物を製造する方法に関する。 [0013] Further, the present invention provides at least (1) 1- [3-[(4,6 dimethoxypyrimidine-2-ylcarbamoyl) sulfamoyl] -2-pyridyl] -2-fluoropropyl methoxyacetate , N- [(4, 6 dimethoxypyrimidine 1-2-yl) aminocarbol] — 2— (2 fluoro — 1 hydroxypropyl) 1 3 pyridinesulfonamide and at least one selected from the group consisting of their salt strength At least one sulfonic acid selected from the group consisting of (2) inorganic salts, (3) aryl sulfonates, alkyl aryl sulfonates and their formalin condensates The present invention relates to a method for producing an aqueous suspension herbicidal composition by mixing a salt and (4) water and, if desired, wet milling.
発明の効果  The invention's effect
[0014] 本発明により、水性懸濁状除草組成物中において除草性スルホニルゥレア系化合 物又はその塩の分解が抑制され、かつ製剤の懸濁性が十分保たれた水性懸濁状除 草組成物及びそれを用いた除草方法を提供することができる。更に本発明では、製 剤の各成分を混合して、所望により湿式粉砕することにより水性懸濁状除草組成物 を調製することができ、有効成分を一旦溶解させ、再沈殿させるなどの煩雑な製造ェ 程を要しない。  [0014] According to the present invention, an aqueous suspension herbicide in which the decomposition of the herbicidal sulfonylurea compound or a salt thereof is suppressed in the aqueous suspension herbicidal composition and the suspension of the preparation is sufficiently maintained. A composition and a herbicidal method using the composition can be provided. Furthermore, in the present invention, an aqueous suspension herbicidal composition can be prepared by mixing each component of the preparation and optionally wet-grinding, so that the active ingredient is once dissolved and reprecipitated. No manufacturing process is required.
発明を実施するための最良の形態  BEST MODE FOR CARRYING OUT THE INVENTION
[0015] 本発明に使用される、除草性スルホ -ルゥレア系化合物は、 1 [3— [ (4,6—ジメト キシピリミジン— 2—ィルカルバモイル)スルファモイル]— 2—ピリジル]— 2—フルォロ プロピル メトキシアセテート、即ち、一般名フルセトスルフロン (flucetosulforon、以下 化合物 Al)、 N— [(4, 6 ジメトキシピリミジン— 2—ィル)ァミノカルボ-ル]— 2— (2 フルォロ 1 ヒドロキシプロピル) 3 ピリジンスルホンアミド(以下化合物 A2) 又はそれらの塩であり、当該塩としては、種々のものが挙げられる。例えばナトリウム、 カリウムなどのアルカリ金属との塩;マグネシウム、カルシウムなどのアルカリ土類金属 との塩;モノメチルァミン、ジメチルァミン、トリェチルァミンなどのァミンとの塩などが挙 げられる。 [0015] The herbicidal sulfo-lurea compound used in the present invention is 1 [3— [(4,6-Dimethyoxypyrimidine-2-ylcarbamoyl) sulfamoyl] -2-cyclopyridyl] -2-fluoropropyl. Methoxy acetate, ie, generic name flucetosulforon (compound Al), N — [(4, 6 Dimethoxypyrimidine—2-yl) aminocarbo] — 2— (2 Fluoro 1 hydroxypropyl) 3 Pyridine sulfone It is an amide (hereinafter referred to as Compound A2) or a salt thereof. Examples of the salt include various salts. For example, salts with alkali metals such as sodium and potassium; salts with alkaline earth metals such as magnesium and calcium; salts with amines such as monomethylamine, dimethylamine and triethylamine.
[0016] 本発明に使用される、無機塩としては、種々のものが挙げられる。例えば、リン酸ァ ルカリ金属塩、リン酸アルカリ土類金属塩などがある。これらのうち、望ましくはリン酸 アルカリ金属塩であり、これらの中でも更に望ましくは、リン酸二水素ナトリウムやリン 酸二水素カリウムなどである。  [0016] Various inorganic salts are used in the present invention. For example, there are alkali metal phosphates and alkaline earth metal phosphates. Of these, alkali metal phosphates are desirable, and among these, sodium dihydrogen phosphate and potassium dihydrogen phosphate are more desirable.
[0017] 本発明に使用される、スルホン酸塩類におけるアルキル部分としては、直鎖状のも のでも、分枝状のものでもよい。例えば、メチル、ェチル、プロピル、ブチル、ペンチ ル、へキシル、ヘプチル、ォクチル、ノニル、デシル、ゥンデシル、ドデシルなどの C 〜c のものが挙げられる。 [0017] The alkyl moiety in the sulfonates used in the present invention may be a linear one. However, it may be branched. Examples thereof include those having C to c such as methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl and the like.
12  12
[0018] 上記スルホン酸塩類におけるァリール部分としては、ベンゼン環又はナフタレン環 のような単環式または多環式のようなものが挙げられる。  [0018] Examples of the aryl moiety in the sulfonates include monocyclic or polycyclic compounds such as a benzene ring or a naphthalene ring.
[0019] 上記スルホン酸塩類の塩としては、種々のものが挙げられる。例えばナトリウム、カリ ゥムなどのアルカリ金属との塩;マグネシウム、カルシウムなどのアルカリ土類金属との 塩などがある。 [0019] Examples of the sulfonate salts include various salts. Examples include salts with alkali metals such as sodium and potassium; salts with alkaline earth metals such as magnesium and calcium.
[0020] 上記スルホン酸塩類としては、望ましくは、アルキルァリールスルホン酸塩又はその ホルマリン縮合物であり、更に望ましくは、アルキルベンゼンスルホン酸塩、アルキル ナフタレンスルホン酸塩、アルキルベンゼンスルホン酸塩ホルマリン縮合物、アルキ ルナフタレンスルホン酸塩ホルマリン縮合物である。これらの中でも更に望ましくは、 アルキルベンゼンスルホン酸塩ホルマリン縮合物、アルキルナフタレンスルホン酸塩 ホルマリン縮合物である。  [0020] The sulfonates are preferably alkylaryl sulfonates or formalin condensates thereof, more preferably alkylbenzene sulfonates, alkyl naphthalene sulfonates, alkylbenzene sulfonate formalin condensates, It is an alkyl naphthalene sulfonate formalin condensate. Among these, alkylbenzene sulfonate formalin condensate and alkyl naphthalene sulfonate formalin condensate are more desirable.
[0021] 本発明の水性懸濁状除草組成物は、所望により各種補助剤を配合することもでき る。各種補助剤としては、当該技術分野で用いられるものであれば、いずれのもので もよい。例えば、前記スルホン酸塩類以外の他の界面活性剤、溶剤、沈降防止剤、 増粘剤、消泡剤、凍結防止剤、ゲル化剤、分散安定剤、薬害軽減剤、防黴剤、防腐 剤、無機アンモニゥム塩類などが挙げられる。これら各種補助剤の具体例としては、 例えば以下のものなどが挙げられる。尚、製剤調製は、当該技術分野における通常 の方法に準じて行うことができる。  [0021] The aqueous suspension herbicidal composition of the present invention may contain various adjuvants as desired. Various adjuvants may be used as long as they are used in the technical field. For example, surfactants other than the sulfonates, solvents, anti-settling agents, thickeners, antifoaming agents, antifreezing agents, gelling agents, dispersion stabilizers, safeners, antifungal agents, antiseptics And inorganic ammonium salts. Specific examples of these various adjuvants include the following. The preparation of the preparation can be performed according to a usual method in the technical field.
[0022] 他の界面活性剤としては、例えば脂肪酸塩、安息香酸塩、アルキルスルホコハク酸 塩、ジアルキルスルホコハク酸塩、ポリカルボン酸塩、アルキル硫酸エステル塩、アル キル硫酸塩、アルキルジグリコールエーテル硫酸塩、アルコール硫酸エステル塩、ァ ルキルスルホン酸塩、リグ-ンスルホン酸塩、アルキルジフヱ-ルエーテルジスルホ ン酸塩、ポリスチレンスルホン酸塩、アルキルリン酸エステル塩、アルキルァリールリン 酸塩、スチリルァリールリン酸塩、ポリオキシエチレンアルキルエーテル硫酸エステル 塩、ポリオキシエチレンアルキルァリールエーテル硫酸塩、ポリオキシエチレンスチリ ルァリールエーテル硫酸塩、ポリオキシエチレンスチリルァリールエーテル硫酸アン モ -ゥム塩、ポリオキシエチレンアルキルァリールエーテル硫酸エステル塩、ポリオキ シエチレンアルキルエーテルリン酸塩、ポリオキシエチレンアルキルァリールリン酸ェ ステル塩、ポリオキシエチレンスチリルァリールエーテルリン酸エステル又はその塩、 フエノールスルホン酸ホルマリン縮合物の塩、アルキルマレイン酸塩ブロックポリマー のような陰イオン系の界面活性剤;ソルビタン脂肪酸エステル、グリセリン脂肪酸エス テル、脂肪酸ポリダリセライド、脂肪酸アルコールポリダリコールエーテル、アセチレン グリコール、アセチレンアルコール、ォキシアルキレンブロックポリマー、ポリオキシェ チレンアルキルエーテル、ポリオキシエチレンアルキルァリールエーテル、ポリオキシ エチレンスチリルァリールエーテル、ポリオキシエチレングリコールアルキルエーテル 、ポリオキシエチレン脂肪酸エステル、ポリオキシエチレンソルビタン脂肪酸エステル 、ポリオキシエチレンソルビトール脂肪酸エステル、ポリオキシエチレングリセリン脂肪 酸エステル、ポリオキシエチレン硬化ヒマシ油、ポリオキシエチレンヒマシ油、ポリオキ シプロピレン脂肪酸エステルのような非イオン系の界面活性剤;アルコキシルイ匕脂肪 族ァミンのようなカチオン系の界面活性剤などが挙げられる。所望によりこれらの 2種 以上を適宜混用してもよい。 [0022] Other surfactants include, for example, fatty acid salts, benzoates, alkylsulfosuccinates, dialkylsulfosuccinates, polycarboxylates, alkyl sulfate esters, alkyl sulfates, alkyl diglycol ether sulfates. , Alcohol sulfate, alkyl sulfonate, lignosulfonate, alkyl diphenyl ether disulfonate, polystyrene sulfonate, alkyl phosphate ester, alkyl aryl phosphate, styryl aryl phosphate Salt, polyoxyethylene alkyl ether sulfate ester salt, polyoxyethylene alkyl aryl ether sulfate salt, polyoxyethylene polystyrene Ruaryl ether sulfate, polyoxyethylene styryl aryl ether sulfate ammonium salt, polyoxyethylene alkyl aryl ether sulfate ester, polyoxyethylene alkyl ether phosphate, polyoxyethylene alkyl aryl phosphate Steionic salts, polyoxyethylene styryl aryl ether phosphates or salts thereof, salts of phenolsulfonic acid formalin condensates, anionic surfactants such as alkyl maleate block polymers; sorbitan fatty acid esters, glycerin fatty acid esters Tellurium, fatty acid polydaricelide, fatty acid alcohol polydalicol ether, acetylene glycol, acetylene alcohol, oxyalkylene block polymer, polyoxyethylene alkyl ether, polyoxyethylene Tylene alkyl aryl ether, polyoxyethylene styryl ether, polyoxyethylene glycol alkyl ether, polyoxyethylene fatty acid ester, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene sorbitol fatty acid ester, polyoxyethylene glyceryl fatty acid ester, polyoxy Nonionic surfactants such as ethylene hydrogenated castor oil, polyoxyethylene castor oil, and polyoxypropylene fatty acid ester; and cationic surfactants such as alkoxy Louis aliphatic amine. If desired, two or more of these may be mixed as appropriate.
[0023] 沈降防止剤としては、例えばシリカ、有機ベントナイト(Bentonite-alkylamino compl ex)、ベントナイト、ホワイトカーボン、アルミニウムマグネシウムケィ酸などが挙げられ る。所望によりこれらの 2種以上を適宜混用してもよい。 [0023] Examples of the anti-settling agent include silica, organic bentonite (Bentonite-alkylamino complex), bentonite, white carbon, and aluminum magnesium caustic acid. If desired, two or more of these may be mixed as appropriate.
増粘剤としては、例えばキサンタンガム、グァーガムのようなヘテロポリサッカライド; ポリビュルアルコール、カルボキシメチルセルロースナトリウム塩、アルギン酸ナトリウ ム塩のような水溶性ポリマー;ベントナイト、ホワイトカーボンなどが挙げられる。所望 によりこれらの 2種以上を適宜混用してもよい。  Examples of the thickener include heteropolysaccharides such as xanthan gum and guar gum; water-soluble polymers such as polybulal alcohol, sodium carboxymethylcellulose and sodium alginate; bentonite and white carbon. If desired, two or more of these may be mixed as appropriate.
[0024] 消泡剤としては、例えばポリジメチルシロキサン、アセチレンアルコールなどが挙げ られる。所望によりこれらの 2種以上を適宜混用してもよい。 [0024] Examples of the antifoaming agent include polydimethylsiloxane and acetylene alcohol. If desired, two or more of these may be mixed as appropriate.
凍結防止剤としては、例えばエチレングリコール、プロピレングリコール、グリセリン、 尿素などが挙げられる。所望によりこれらの 2種以上を適宜混用してもよい。  Examples of the antifreezing agent include ethylene glycol, propylene glycol, glycerin, urea and the like. If desired, two or more of these may be mixed as appropriate.
防腐剤としては、例えばホルマリン、パラクロロメタキシレノール、 1,2-ベンズイソチア ゾリン- 3-オンなどが挙げられる。所望によりこれらの 2種以上を適宜混用してもよい。 Examples of preservatives include formalin, parachlorometaxylenol, 1,2-benzisothia Zolin-3-one and the like. If desired, two or more of these may be mixed as appropriate.
[0025] 溶剤としては、例えばプロパノール、イソブタノールのような 1価アルコール類;ェチ レングリコール、プロピレングリコール、ジエチレングリコール、へキシレングリコール、 ポリエチレングリコール、ポリプロピレングリコール、グリセリンのような多価アルコール 類;プロピルセロソルブ、ブチルセ口ソルブ、フエ-ルセ口ソルブ、プロピレングリコー ノレモノメチノレエーテノレ、プロピレングリコーノレモノェチノレエーテノレ、プロピレングリコー ルモノプロピルエーテル、プロピレングリコールモノブチルエーテル、プロピレングリコ ールモノフエ-ルエーテルのようなグリコールエーテル類;ジォキサンのようなエーテ ル類;シクロへキサノン、メチルイソブチルケトンのようなケトン類;酢酸、酪酸のような 脂肪酸;酢酸イソプロピル、酢酸ブチルのようなエステル類; N—メチルホルムアミド、 N—メチルピロリドン、ジメチルスルホキシド、 1, 3—ジメチルー 2—イミダゾリジノン、 アミン類、エーテルァミン類のような含窒素'含硫黄溶剤;ノルマルパラフィン、イソパ ラフィンのような脂肪族炭化水素;アルキルベンゼン、アルキルナフタレン、フエ-ル キシリルェタンような芳香族炭化水素などが挙げられる。所望によりこれらの 2種以上 を適宜混用してもよい。 [0025] Examples of the solvent include monohydric alcohols such as propanol and isobutanol; polyhydric alcohols such as ethylene glycol, propylene glycol, diethylene glycol, hexylene glycol, polyethylene glycol, polypropylene glycol, and glycerin; propyl Such as cellosolve, butylcerosolve, ferrulecetosolve, propylene glycol monomethino ethenore, propylene glycol monomethino enoate, propylene glycol monopropyl ether, propylene glycol monobutyl ether, propylene glycol monophenol ether Glycol ethers; Ethers such as dioxane; Ketones such as cyclohexanone and methyl isobutyl ketone; Fatty acids such as acetic acid and butyric acid Esters such as isopropyl acetate and butyl acetate; nitrogen-containing sulfur-containing solvents such as N-methylformamide, N-methylpyrrolidone, dimethyl sulfoxide, 1,3-dimethyl-2-imidazolidinone, amines and etheramines Aliphatic hydrocarbons such as normal paraffin and isoparaffin; aromatic hydrocarbons such as alkylbenzene, alkylnaphthalene, and phenylsilylethane. If desired, two or more of these may be used as appropriate.
[0026] 本発明においては、所望により、前記除草性スルホニルゥレア系化合物又はその 塩以外の他の除草性ィ匕合物を混用或は併用することができ、この場合に一層優れた 効果、作用性を示すことがある。例えば、適用草種の範囲、薬剤処理の時期、除草 活性等を好ましい方向へ改良できる場合がある。尚、除草性スルホ -ルゥレア系化 合物又はその塩と他の除草性ィ匕合物は、各々別々に製剤したものを散布時に混合 して使用しても、両者を一緒に製剤した水性懸濁状混合除草組成物として使用して ちょい。  [0026] In the present invention, if desired, other herbicidal compounds other than the herbicidal sulfonylurea compound or a salt thereof can be mixed or used together, and in this case, a further excellent effect, May exhibit activity. For example, the range of applicable grass species, the timing of chemical treatment, herbicidal activity, etc. may be improved in the preferred direction. It should be noted that the herbicidal sulfo-lurea compound or its salt and other herbicidal compounds may be used separately in the form of a mixture prepared at the time of spraying. Use it as a turbid mixed herbicidal composition.
本発明には、前記した水性懸濁状混合除草性組成物及び該組成物を用いて望ま しくない植物を防除又はその生育を抑制する方法も含まれる。また本発明には、除草 性スルホニルゥレア系化合物又はその塩と他の除草性ィ匕合物を各々別々に製剤し たものを用いて、望ましくない植物を防除又はその生育を抑制する方法も含まれる。  The present invention includes the above-described aqueous suspension mixed herbicidal composition and a method for controlling undesired plants or suppressing the growth thereof using the composition. In addition, the present invention also includes a method for controlling undesired plants or suppressing the growth thereof by using separately prepared herbicidal sulfonylurea compounds or salts thereof and other herbicidal compounds. included.
[0027] 他の除草性ィ匕合物としては、例えば下記(1)〜(11)の化合物群(一般名;一部 ISO 申請中を含む)から適宜選択することが出来る。特に記載がない場合であっても、こ れら化合物に、塩、アルキルエステル、光学異性体のような各種構造異性体などが 存在する場合は、当然それらも含まれる。 [0027] Other herbicidal compounds can be selected as appropriate from, for example, the following compound groups (1) to (11) (generic names; some including those in the application for ISO). Even if there is no specific description, this When these compounds contain various structural isomers such as salts, alkyl esters and optical isomers, they are naturally included.
[0028] (1) 2,4- D、 2,4- DBゝ 2,4- DPゝ MCPA、 MCPB、 MCPP、ナプロア-リド(naproanilide) 、クロメプロップ(clomeprop)のようなフエノキシ系; 2,3,6-TBA、ジカンパ(dicamba)、 ジクロべ-ル(dichlobenil)、ピクロラム(picloram)、トリクロピル (triclopyr)、クロビラリド (clopyralid)、ァミノビラリド(aminopyralid)のような芳香族カルボン酸系;ナプタラム(n aptalam)、べナゾリン (benazolin)、 = ンクロフック (quinclorac)、ゃン フック (quinmerac )、ダイフノレフェンゾピノレ (diflufenzopyr)、チアゾピノレ (thiazopyr)などのように植物の ホルモン作用を攪乱することで除草効力を示すとされているもの。  [0028] (1) 2,4-D, 2,4-DB ゝ 2,4-DP ゝ MCPA, MCPB, MCPP, phenoxy systems such as naproanilide, clomeprop; 2,3 , 6-TBA, aromatic carboxylic acids such as dicamba, dichlobenil, picloram, triclopyr, clopyralid, aminopyralid; naptalam ), Benazolin, = quinclorac, nyanhook (quinmerac), diflufenzopynore, thiazopyr, etc. What is supposed to indicate.
[0029] (2)クロロトルロン (chlorotoluron)、ジゥロン(diuron)、フルオメッロン (fluometuron)、リ -ュロン (linuron)、イソプロチュロン (isoproturon)、メ卜べンズロン (metobenzuron)、 テブチウロン (tebuthiuron)のような尿素系;シマジン(simazine)、アトラジン(atrazine) 、アトラトン(atratone)、シメトリン(simetryn)、プロメトリン(prometryn)、ジメタメトリン(d imethametryn)、へキサジノン (hexazinone)、メトリブジン (metribuzin)、テノレブチラジン (terbuthylazine)、、ノーナンン (cyanazine)、 メトリン (ametryn)、ンブトリン (cybutryne )、トリアジフラム(triaziflam)、プロパジン(propazine)のようなトリアジン系;ブロマシル (bromacil)、レナシル(lenacil)、ターバシル (terbacil)、のようなゥラシル系;プロパ-ル (propanil)、シプロミツド(cypromid)のようなァ-リド系;スエップ(swep)、デスメディフ アム (desmedipham)、フェンメディファム (phenmedipham)のようなカーノメート系;ブロ モキシニノレ (bromoxynil)、ブロモキシニノレ 'オタタノエート (bromoxynn- octanoate)、了 ィォキシ-ル(ioxynil)のようなヒドロキシベンゾ-トリル系;ピリデート(pyridate)、ベン タゾン (bentazone)、アミカノレバゾン (amicarbazone)、メタゾーノレ (methazole)などのよ うに植物の光合成を阻害することで除草効力を示すとされて 、るもの。 [0029] (2) such as chlorotoluron, diuron, fluometuron, linuron, isoproturon, metobenzuron, tebuthiuron Urea: Simazine, atrazine, atratone, simetryn, prometryn, dimeththametryn, hexazinone, metribuzin, tenolebutyrazine, terbuthylazine , Nonazine (cyanazine), metrin (ametryn), nbutrin (cybutryne), triaziflam, propazine (propazine) and other triazines; System; propanil, cypromid and other arrid systems; swep, death Carnomate systems such as desmedipham and phenmedipham; hydroxybenzo-tolyl systems such as bromoxynil, bromoxynn-octanoate and i oxyn il A herbicidal activity that inhibits plant photosynthesis, such as pyridate, bentazone, amikabolezone, and methazole.
[0030] (3)それ自身が植物体中でフリーラジカルとなり、活性酸素を生成させて速効的な 除草効力を示すとされているパラコート(paraquat)、ジクワット(diquat)のような 4級ァ ンモニゥム塩系。  [0030] (3) A quaternary ammonia such as paraquat or diquat, which is said to be a free radical in the plant itself, generating active oxygen and exhibiting rapid herbicidal efficacy. Salt system.
[0031] (4)ニトロフェン(nitrofen)、クロメトキシフェン(chlomethoxyfen)、ビフエノックス (bife nox)、アシフルオルフエンナトリウム塩(acifluorfen- sodium)、ホメサフェン(fomesafen) 、ォキシフルオルフエン(oxyfluorfen)、ラタトフェン(lactofen)、エトキシフェンェチル( ethoxyfen-ethyl)のようなジフエ-ルエーテル系;クロルフタリム(chlorphthalim)、フル ミオキサジン(flumioxazin)、フノレミクロラックペンチノレ(flumiclorac- pentyl)、フノレチア セットメチル(fluthiacet- methyl)のような環状イミド系;ォキサジアルギル(oxadiargyl) 、ォキサジァゾン(oxadiazon)、スルフェントラゾン(sulfentrazone)、カルフェントラゾン ェチノレ (carfentrazone-ethyl)、チジアジミン (thidiazimin)、ペントキサゾン (pentoxazo ne)、ァザフエ-ジン(azafenidin)、イソプロパゾール(isopropazole)、ピラフノレフェンェ チル(pyraflufen- ethyl)、ベンズフェンジゾン(benzfendizone)、ブタフエナシル(butafe nacil)、メトべンズロン (metobenzuron)、シ-ドンェチノレ (cinidon— ethyl)、フノレポキサ ム(flupoxam)、フルァゾレート(fluazolate)、プロフルァゾール(profluazol)、ピラクロ- ノレ (pyrachlonil)、フルフェンピルェチル (flufenpyr- ethyl)、ベンカルノ ゾン (bencarba zone)などのように植物のクロロフィル生合成を阻害し、光増感過酸化物質を植物体 中に異常蓄積させることで除草効力を示すとされて 、るもの。 [0031] (4) Nitrofen, Chlomethoxyfen, Bife nox, Acifluorfen-sodium, Fomesafen , Dioxyethers such as oxyfluorfen, latofen, ethoxyfen-ethyl; chlorphthalim, flumioxazin, funole microlac pentinole ( Cyclic imides such as flumiclorac-pentyl, flutiacet-methyl; oxadiargyl, oxadiazon, sulfentrazone, carfentrazone-ethyl, thidazimine (thidiazimin), pentoxazone, azafenidin, isopropazole, pyraflufen-ethyl, benzfendizone, butafe nacil, meth Bentoslon (metobenzuron), Shidonetonore (cinidon—ethyl), Funore Plant chlorophyll biosynthesis such as flapoxam, fluazolate, profluazol, pyrachlonil, flufenpyr-ethyl, bencarbazone, etc. It is said to show herbicidal activity by inhibiting and abnormally accumulating photosensitized peroxide in the plant body.
[0032] (5)ノルフルラゾン(norflurazon)、クロリダゾン(chloridazon)、メトフルラゾン(metflur azon)のようなピリダジノン系;ピラゾレート(pyrazolate)、ピラゾキシフェン(pyrazoxyfe n)、ベンゾフエナップ(benzofenap)、トプラメゾン(topramezone、 BAS-670H)、ピラス ルフォトール(pyrasulfotole)のようなピラゾール系;アミトロール (amitrol)、フルリドン(11 uridone)、フルルタモン(flurtamone)、ジフルフエ-カン(diflufenican)、メトキシフエノ ン (methoxyphenone)、ク Pマゾン (clomazone)、スノレ 卜ジ才ン (sulcotrione)、メソ卜ジ才 ン(mesotrione)、 AVH- 301、イソキサフルトール (isoxaflutole)、ジフェンゾコート(difen zoquat)、イソキサクロロト一ノレ (isoxachlortole)、ベンゾビシクロン (benzobicyclon)、ピ コリナフェン(picolinafen)、ビフルブタミド(beflubutamid)などのようにカロチノイドなど の植物の色素生合成を阻害し、白化作用を特徴とする除草効力を示すとされている もの。 [0032] (5) Pyridazinones such as norflurazon, chloridazon, metflur azon; pyrazolate, pyrazoxifene, benzofenap, topramezone, BAS -670H), pyrazoles such as pyrasulfotole; amitrol, fluridone (11 uridone), flurtamone, diflufenican, methoxyphenone, clomazone , Sulcotrione, mesotrione, AVH-301, isoxaflutole, difen zoquat, isoxachlorotole, benzobicyclon , Carotenoids such as picolinafen and biflubutamid It inhibits pigment biosynthesis of plants such as and shows herbicidal efficacy characterized by whitening.
[0033] (6)ジクロホップメチル(diclofop- methyl)、フラムプロップェムメチル (flamprop- M- m ethyl),ピリフエノッブナトリウム塩(pyriphenop-sodium)、フルアジホップブチル(fluazif op-butyl)、 ノヽロキシホップメチノレ (haloxyfop- methyl)、キザロホップェチノレ (quizalofo p- ethyl)、シハロホップブチノレ(cyhalofop- butvl)、フエノキサプロップェチノレ(fenoxapr op-ethyl)、メタミホッププロピル(metamifop- propyl)のようなァリールォキシフエノキシ プロピオン酸系;ァロキシジムナトリウム塩(alloxydim- sodium)、クレソジム(clethodim) 、セトキシジム(sethoxydim)、トラノレコキシジム(tralkoxydim)、ブトロキシジム(butroxy dim)、テプラロキシジム(tepraloxydim)、カロキシジム(caloxydim)、クレフォキシジム( clefoxydim)、プロホキシジム(profoxydim)のようなシクロへキサンジオン系などのよう にイネ科植物に特異的に除草効力が強く認められるもの。 [0033] (6) Dicloofop-methyl, flamprop-M-methyl, pyriphenop-sodium, fluazif op-butyl , Oxyloxyhop-methyl, quizalofo p-ethyl, cyhalofop-butvl, fenoxapr-petinole op-ethyl, metalifop-propyl and other aryloxyphenoxy propionic acid systems; alloxydim-sodium, clethodim, sethoxydim, tranoleco Specific to gramineous plants such as troxyxydim, butroxydim, tepraloxydim, caloxydim, clefoxydim, and cyclohexenedione such as profoxydim Strong herbicidal efficacy is recognized.
(7)クロリムロンェチノレ (chlorimuron-ethyl)、スノレホメッロンメチノレ(sulfometuron— me thyl)、プリミスルフロンメチル(primisulforon- methyl)、ベンスルフロンメチル(bensulfo ron-methyl)、クロノレスノレフロン (chlorsulforon)、メトスノレフロンメチノレ (metsulforon— me thyl)、シノスノレフロン(cinosulforon)、ピラゾスルフロンェチル(pyrazosulforon- ethyl) 、アジムスルフロン(azimsulforon)、フラザスルフロン(flazasulforon)、リムスルフロン(ri msulfuron)、ニコスノレフロン (nicosul!Uron)、イマゾスノレフロン (imazosulfuron)、シクロ スルファムロン(cyclosulfamuron)、プロスルフロン(prosulforon)、フルピルスルフロン( flupyrsulluron)、トリフルスルフロンメチル(triflusulforon- methyl)、ハロスルフロンメチ ノレ(halosulforon- methyl)、チフェンスノレフロンメチノレ(thifensulforon- methyl)、ェトキ シスルフロン(ethoxysulforon)、ォキサスルフロン(oxasulforon)、ェタメトスルフロン(et hametsulfuron 、ィォドスノレフロン uodosulfuron)、スノレフォスノレフロン sulfosulfuron 、 トリアスルフロン(triasulforon)、トリべヌロンメチル(tribenuron- methyl)、トリトスルフロ ン(tritosulforon)、フォーラムスルフロン(foramsulforon)、トリフルォキシスルフロン(tri floxysulluron)、イソスノレフロンメチノレ(isosulforon- methyl)、メソスノレフロンメチノレ(mes osulfuron— methyl)、才ノレソスノレファムロン (orthosulfamuron)、ァ ドスノレフロン、 amidos ulluron)のようなスルホ -ルゥレア系;フルメッラム(flumetsulam)、メトスラム(metosula m)、ジクロスラム (diclosulam)、クロランスラムメチノレ (cloransulam- methyl)、フロラスラ ム(florasulam)、メトスノレフアム(metosulfam)、ぺノキススラム (penoxsulam)のようなトリ ァゾロピリミジンスルホンアミド系;イマザピル(imazapyr)、イマゼタピル(imazethapyr) 、ィマザキン (imazaquin)、ィマサモッタス (imazamox)、ィマザメス (imazamethリ、ィマ ザメタべンズ(imazamethabenz)、イマザピック(imazapic)のようなイミダゾリノン系;ピリ チォバックナトリウム塩(pyrithiobac- sodium)、ビスピリバックナトリウム塩(bispyribac- s odium)、ピリミノノ ックメチノレ (pyriminobac— methyl)、ピリべンゾキシム (pyribenzoxim) 、ピリフタリド(pyriftalid)、ピリミスルファン(pyrimisulfan、 KUH- 021)のようなピリミジ- ルサリチル酸系;フルカーバゾン(flucarbazone)、プロカーバゾンソディウム(procarba zone-sodium)のようなスルホ -ルァミノカルボ-ルトリアゾリノン系;グリホサート(glyph osate)、グリホサートアンモ-ゥム塩(glyphosate- ammonium)、グリホサートイソプロピ ノレ, ン; ¾ ( glyphos ate-is opropylamine)、スルホサ ~~ト (sulfosate)、クルホシネ ~~ト (gl ufosinate)、グノレホシネートアンモ-ゥム塩 (glufosinate- ammonium)、ビラナホス (bilan afos)などのように植物のアミノ酸生合成を阻害することで除草効力を示すとされてい るもの。 (7) Chlorimuron-ethyl, sulhomeromon-me thyl, primisulforon-methyl, bensulfo ron-methyl, chronoles Noreflon (chlorsulforon), Methos no lefon metinore (metsulforon-me thyl), Shinosno leflon (cinosulforon), pyrazosulforon-ethyl, azimsulforon, flazasulforon (flazasulforon), rimsulfuron (flazasulforon) ri msulfuron), nicosulofuron (nicosul! Uron), imazosulfuron (imazosulfuron), cyclosulfamuron (cyclosulfamuron), prosulforon (prosulforon), flupirsulfuron (flupyrsulluron), triflusulfuron-methyl (triflusulforon-methyl), Halosulforon-methyl, thifensulforon- methyl), ethoxysulforon, oxasulforon, ethametsulfuron, iodosnorephron uodosulfuron, snolefosnoreflon sulfosulfuron, triasulforon, tribenuron methyl (tribenuron methyl) , Tritosulforon, foramsulforon, tri floxysulluron, isosulforon-methyl, mesosulfuron-methyl, talent noresosno Sulfo-Rulea like orthosulfamuron, amidos ulluron; flumetsulam, metosula m, diclosulam, cloransulam-methyl, florasulam ( florasulam), Metosulfam ), Trioxolopyrimidinesulfonamides such as penoxsulam; imazapyr, imazethapyr, imazaquin, imazamox, imazameth, imazameth, imazameth ), Imidazolinones such as imazapic; pyrithiobac-sodium, bispyribac-s odium), pyriminobac-methyl, pyribenzoxim, pyriftalid, pyrimisulfane (pyrimisulfan, KUH-021) and other pyrimidyl-rusalicylic acid series; flucarbazone, procarbazone Sulfo-luminocarbo-triazolinones such as procarba zone-sodium; glyphosate, glyphosate-ammonium salt, glyphosate-isopropylamine, ¾ (glyphos ate-is opropylamine), Inhibiting plant amino acid biosynthesis, such as sulfosate, glufosinate, glufosinate-ammonium salt, and bilanafos It is said that it shows herbicidal efficacy.
[0035] (8)トリフルラリン (trifluralin)、オリザリン(oryzalin)、ニトラリン(nitralin)、ペンディメ タリン(pendimethalin)、ェタルフルラリン(ethalfluralin)、ベンフルラリン(benfluralin)、 プロジァミン(prodiamine)のようなジ-トロア-リン系;ベンスリド(bensulide)、ナプロナ ミド(napronamide)、プロナミド(pronamide)のようなアミド系;アミプロホスメチル(amipr ofos— methyl)、ブタ ホス (butamifos)、ァ-ロホス、anilofos)、ヒぺロホス、piperophos) のような有機リン系;プロファム(propham)、クロルプロファム (chlorpropham)、バーバ ン(barban)のようなフエ-ルカーバメート系;ダイムロン(daimuron)、クミノレロン (cumyl uron)、ブロモブチド (bromobutide)のようなクミルァミン系;ァシュラム(asulam)、ジチ ォピル(dithiopyr)、チアゾピル(thiazopyr)、カフエンストロール(cafenstrole)、インダ ノファン (indanofan)などのように植物の細胞有糸分裂を阻害することで除草効力を示 すとされているもの。  [0035] (8) Di-troaline systems such as trifluralin, oryzalin, oritalin, nitraline, pendimethalin, ethalfluralin, benfluralin, prodiamine Amides such as bensulide, napronamide, pronamide; amiprofos-methyl, butamifos, alofos, hyperophos, Organophosphorus such as piperophos; phelocarbamates such as propham, chlorpropham, and barban; daimuron, cumyluron, bromobutide Cumylamines such as asuram, dithiopyr, thiazopyr, cafenst role), indanofan, etc., which are said to show herbicidal efficacy by inhibiting cell mitosis in plants.
[0036] (9)ァラクロ一ノレ (alachlor)、メタザクローノレ (metazachlor)、ブタクローノレ (butachlor プレチラクロール(pretilachlor)、メトラクロール(metolachlor)、 S—メトラクロール(S — metolachlor)、テ-ノレクローノレ (thenylchlor)、ぺトキサマイド (pethoxamid)、ァセトク口 一ノレ (acetochlor)、プロノ《クローノレ (propachlor)、プロピソクローノレ (propisochlor)のよ うなクロロアセトアミド系;モリネート(molinate)、ジメピぺレート(dimepiperate)、ピリブ チカルブ(pyributicarb)のようなカーバメート系;エトベンザ-ド(etobenzanid)、メフエ ナセット(mefenacet)、フノレフエナセット(flufenacet)、トリディファン(tridiphane)、フエ ントラザミド(fentrazamide)、ォキサジクロメフォン(oxaziclomefone)、ジメテナミド(dime thenamid)、ベンフレセート [0036] (9) arachlor, metazachlor, butachlor pretilachlor, metolachlor, S-metolachlor, S-metolachlor, tenenylchlor, Chloroacetamides, such as toxamide, pettoxamide, acetochlor, prono << chlorate (propachlor), propisoclonole (propisochlor); ) Carbamates such as: etobenzanid, mefenacet, flufenacet, tridiphane, fentrazamide, oxaziclomefone, Dimethenamide thenamid), ben fresate
(benforesate)などのように植物のタンパク質生合成あるいは脂質生合成を阻害するこ とで除草効力を示すとされているもの。  (benforesate), etc. that are said to show herbicidal efficacy by inhibiting plant protein biosynthesis or lipid biosynthesis.
[0037] (10) EPTC、ブチレート (butylate)、ベルノレート(vernolate)、ぺブレート (pebulate) 、シクロエート (cycloate)、プロスルホカノレブ (prosulfocarb)、エスプロカノレブ (esproca rb)、チォベンカノレブ(thiobencarb)、ジァレート(diallate)、トリアレート(triallate)のよ うなチォカーバメート系; MSMA、 DSMA、エンドタール(endothall)、エトフメセ一ト( etho!Umesate)、ソティゥムクロレート (sodium chlorate)、ベフルゴン酸 (pelargonic ac id)、ホスァミン(fosamine)、ピノキサデン(pinoxaden)、 HOK- 201など。  [0037] (10) EPTC, butylate, vernolate, pebulate, cycloate, prosulfocarb, esprocarb, thiobencarb, dialate Thiocarbamates such as diallate and triallate; MSMA, DSMA, endothal, etho! Umesate, sodium chlorate, befrugonic acid ), Fosamine, pinoxaden, HOK-201 and the like.
[0038] 、丄丄) Xanthomonas campestris. apicoccosurus nematosurus. axseronilum monos eras. Drechsrela mmmsgmsなどのように植物に寄生することで除草効力を示すとさ れているもの。  [0038], 丄 丄) Xanthomonas campestris. Apicoccosurus nematosurus. Axseronilum monos eras. Drechsrela mmmsgms, etc., which are said to show herbicidal efficacy by parasitizing plants.
[0039] 本発明の水性懸濁状除草組成物における、各成分の配合割合は、配合成分の種 類、製剤形態、施用場面などに応じ、適宜変更する場合があるので一概に規定でき ない。しかし、例えば除草性スルホニルゥレア系化合物としての化合物 Al、化合物 A 2又はそれらの塩は 0.1〜60重量部、望ましくは 0.5〜50重量部であり、無機塩は 0.1 〜25重量部、望ましくは 1〜20重量部、さらに望ましくは 2〜10重量部であり、スルホン 酸塩類は、 0.01〜30重量部、望ましくは 0.1〜20重量部であり、残分の主成分は水で ある。  [0039] The blending ratio of each component in the aqueous suspension herbicidal composition of the present invention cannot be specified unconditionally because it may be changed as appropriate according to the type of the blending component, the formulation form, the application scene, and the like. However, for example, Compound Al, Compound A 2 or a salt thereof as a herbicidal sulfonylurea compound is 0.1 to 60 parts by weight, preferably 0.5 to 50 parts by weight, and an inorganic salt is 0.1 to 25 parts by weight, preferably 1 to 20 parts by weight, more preferably 2 to 10 parts by weight, sulfonates are 0.01 to 30 parts by weight, preferably 0.1 to 20 parts by weight, and the remaining main component is water.
[0040] 所望により他の界面活性剤を配合する場合は 0.01〜20重量部、望ましくは 0.1〜15 重量部であり、沈降防止剤を配合する場合は 0.01〜10重量部、望ましくは 0.05〜5重 量部であり、増粘剤を配合する場合は 0.01〜10重量部、望ましくは 0.05〜5重量部で あり、消泡剤を配合する場合は 0.001〜10重量部、望ましくは 0.01〜5重量部であり、 防腐剤を配合する場合は 0.01〜10重量部、望ましくは 0.05〜5重量部であり、溶剤を 配合する場合は 1〜70重量部、望ましくは 1〜50重量部であり、他の除草性化合物を 配合する場合は 0.1〜60重量部、望ましくは 0.1〜50重量部である。  [0040] 0.01 to 20 parts by weight, preferably 0.1 to 15 parts by weight when blended with other surfactants as desired, and 0.01 to 10 parts by weight, preferably 0.05 to 5 parts when blending an anti-settling agent. Part by weight, 0.01 to 10 parts by weight, preferably 0.05 to 5 parts by weight when blending thickeners, 0.001 to 10 parts by weight, desirably 0.01 to 5 parts by weight when blending antifoaming agents 0.01 to 10 parts by weight, preferably 0.05 to 5 parts by weight when preservatives are added, 1 to 70 parts by weight, preferably 1 to 50 parts by weight, etc. When the herbicidal compound is added, it is 0.1 to 60 parts by weight, preferably 0.1 to 50 parts by weight.
[0041] 本発明の水性懸濁状除草組成物は、望ましくない植物又はそれが生育する場所に 施用し、例えば茎葉処理、土壌処理、湛水処理することにより一年生雑草や多年生 雑草など広範囲の有害植物を防除又はその生育を抑制することができる。 [0041] The aqueous suspension herbicidal composition of the present invention is applied to an undesired plant or a place where it grows, and is treated with, for example, a foliage treatment, a soil treatment, or a flooding treatment to produce annual weeds or perennials. A wide range of harmful plants such as weeds can be controlled or their growth can be suppressed.
有害植物としては、例えばィヌビエ、タイヌビエ、メヒシバ、ェノコログサ、アキノエノコ ログサ、ォヒシバ、カラスムギ、セィバンモロコシ、シノ ムギ、ビロードキビ、パラグラス、 ァゼガヤ、イトァゼガヤ、スズメノカタビラ、スズメノテツポゥ、カモジダサなどのイネ科 雑草;コゴメガヤッリ、ハマスゲ、キハマスゲ、ホタルイ、ミズガヤッリ、タマガヤッリ、マ ッバイ、クログワイなどのカャッリグサ科雑草;ゥリカヮ、ォモダカ、ヘラォモダカなどの ォモダカ科雑草;コナギ、ミズァオイなどのミズァオイ科雑草;ァゼナ、アブノメなどの ゴマノハグサ科雑草;キカシダサ、ヒメミソハギなどのミソハギ科雑草;ィチビ、マルバ アサガオ、シロザ、アメリカキンゴジカ、スベリヒュ、ァオビュ、ァォゲイトウ、ェビスダサ 、ィヌホウズキ、サナエタデ、ハコべ、ォナモミ、タネッケバナ、ホトケノザ、ブタクサ、 ヤエムダラ、セィヨウヒノレガオ、チョウセンアサガオ、ェゾノキッネアザミ、エノキダサな どが挙げられる。また、適用範囲は畑地、水田、果樹園、桑畑などの農耕地;山林、 農道、運動場、工場敷地、芝地などの非農耕地と多岐にわたることができる。除草性 スルホ -ルゥレア系化合物としての化合物 Al、化合物 A2又はそれらの塩は、 lhaあ たり lg〜500g、望ましくは 2g〜250gの割合で施用することができる。  Examples of harmful plants include Inubie, Tainubie, Barefoot, Enokorogusa, Akinoenokorogosa, Ohashiba, Oats, Oats, Sowbill, Cypress, Velvet Millet, Paragrass, Azegaya, Itasegaya, Sparrows Mosquitoes, fireflies, staghorns, moths, crabs and weeds; Of Camiaceae; Ichibi, Maruba morning glory, white-tailed, American goldfish, Suberuhi, Aobu, Aguayte, Yebisuda, Inho Examples include zuki bean, sanaetade, chickweed, onamomi, tanekikebana, photokenosa, ragweed, yaemdara, hinoki hinagao, datura, ezonokine thisami, and enoki tasa. The scope of application can be varied from farmland such as upland, paddy fields, orchards, and mulberry fields; non-agricultural land such as forests, farm roads, playgrounds, factory sites, and turf. Herbicidal Compound Al, Compound A2 or a salt thereof as a sulfo-lurea compound can be applied at a rate of 1 to 500 g, preferably 2 to 250 g per lha.
実施例 Example
以下に本発明の実施例を記載する力 本発明はこれらに限定されるものではない。 実施例 1  The ability to describe examples of the present invention below The present invention is not limited to these. Example 1
(1)化合物 A1 (純度 97.9%) 10.0重量部  (1) Compound A1 (Purity 97.9%) 10.0 parts by weight
(2)アルキルナフタレンスルホン酸ナトリウムホルマリン縮合物  (2) Sodium alkylnaphthalene sulfonate formalin condensate
(商品名: Supragil MNS/25、ローディア日華社製) 4.0重量部  (Product name: Supragil MNS / 25, Rhodia Nikka) 4.0 parts by weight
(3)リン酸二水素ナトリウム 7.0重量部  (3) Sodium dihydrogen phosphate 7.0 parts by weight
(4)水 79.0重量部  (4) 79.0 parts by weight of water
以上の成分を混合し、湿式粉砕機で 5分間粉砕して、水性懸濁状除草組成物を得た 実施例 2 Example 2 An aqueous suspension herbicidal composition was obtained by mixing the above ingredients and pulverizing with a wet pulverizer for 5 minutes.
(1)化合物 A1 (純度 97.9%) 5.0重量部  (1) Compound A1 (Purity 97.9%) 5.0 parts by weight
(2)ベンスルフロンメチル(純度 99.3%) 5.0重量部 (3) Supragil MNS/25 (同前) 4.0重量部 (2) Bensulfuron methyl (purity 99.3%) 5.0 parts by weight (3) Supragil MNS / 25 (Same as above) 4.0 parts by weight
(4)シリコーン系消泡剤  (4) Silicone antifoaming agent
(商品名: Rhodorsil 432、ローディア日華社製) 0.1重:! I  (Product name: Rhodorsil 432, manufactured by Rhodia Nikka Co., Ltd.) I
(5)リン酸二水素ナトリウム 7.0重量部  (5) Sodium dihydrogen phosphate 7.0 parts by weight
(6)水 68.9重量部  (6) 68.9 parts by weight of water
(7)キサンタンガム(1.5重量部)及び  (7) xanthan gum (1.5 parts by weight) and
1,2-ベンズイソチアゾリン- 3-オン(1.0重量部)を含む水 10.0重量部 以上の成分を混合し、湿式粉砕機で 5分間湿式粉砕して、水性懸濁状除草組成物を 実施例 3  Example 3 Aqueous suspension herbicidal composition was prepared by mixing 10.0 parts by weight or more of water containing 1,2-benzisothiazolin-3-one (1.0 part by weight) and then wet-grinding it with a wet grinder for 5 minutes.
(1)化合物 A1 (純度 97.9%) 5.0重量部  (1) Compound A1 (Purity 97.9%) 5.0 parts by weight
(2)アジムスルフロン(純度 99.0%) 10.0重量部  (2) Azimusulfuron (purity 99.0%) 10.0 parts by weight
(3) Supragil MNS/25 (同前) 4.0重量部  (3) Supragil MNS / 25 (Same as above) 4.0 parts by weight
(4) Rhodorsil 432 (同前) 0.1重量部  (4) Rhodorsil 432 (same as above) 0.1 parts by weight
(5)リン酸二水素ナトリウム 7.0重量部  (5) Sodium dihydrogen phosphate 7.0 parts by weight
(6)水 63.9重量部  (6) 63.9 parts by weight of water
(7)キサンタンガム(1.5重量部)及び  (7) xanthan gum (1.5 parts by weight) and
1,2-ベンズイソチアゾリン- 3-オン(1.0重量部)を含む水 10.0重量部 以上の成分を混合し、湿式粉砕機で 5分間湿式粉砕して、水性懸濁状除草組成物を 得た。  Water containing 1,2-benzisothiazolin-3-one (1.0 part by weight) 10.0 parts by weight or more of the ingredients were mixed, and wet-pulverized for 5 minutes with a wet pulverizer to obtain an aqueous suspension herbicidal composition.
実施例 4 Example 4
(1)化合物 A1 (純度 97.9%) 5.0重量部  (1) Compound A1 (Purity 97.9%) 5.0 parts by weight
(2)アジムスルフロン(純度 99.0%) 15.0重量部  (2) Azimusulfuron (purity 99.0%) 15.0 parts by weight
(3) Supragil MNS/25 (同前) 4.0重量部  (3) Supragil MNS / 25 (Same as above) 4.0 parts by weight
(4) Rhodorsil 432 (同前) 0.1重量部  (4) Rhodorsil 432 (same as above) 0.1 parts by weight
(5)リン酸二水素ナトリウム 7.0重量部  (5) Sodium dihydrogen phosphate 7.0 parts by weight
(6)水 68.9重量部  (6) 68.9 parts by weight of water
以上の成分を混合し、湿式粉砕機で 5分間粉砕して、水性懸濁状除草組成物を得た [0046] 実施例 5 The above ingredients were mixed and pulverized with a wet pulverizer for 5 minutes to obtain an aqueous suspension herbicidal composition. [0046] Example 5
(1)化合物 A2 10.0重量部  (1) Compound A2 10.0 parts by weight
(2) Supragil MNS/25 (同前) 4.0重量部  (2) Supragil MNS / 25 (same as above) 4.0 parts by weight
(3)リン酸二水素ナトリウム 7.0重量部  (3) Sodium dihydrogen phosphate 7.0 parts by weight
(4)水 79.0重量部  (4) 79.0 parts by weight of water
以上の成分を混合し、湿式粉砕機で 5分間湿式粉砕して、水性懸濁状除草組成物を 得た。  The above ingredients were mixed and wet pulverized with a wet pulverizer for 5 minutes to obtain an aqueous suspension herbicidal composition.
[0047] 比較例 1 [0047] Comparative Example 1
(1)化合物 A1 (純度 97.9%) 10.0重量部  (1) Compound A1 (Purity 97.9%) 10.0 parts by weight
(2) Supragil MNS/25 (同前) 4.0重量部  (2) Supragil MNS / 25 (same as above) 4.0 parts by weight
(3)水 86.0重量部  (3) 86.0 parts by weight of water
以上の成分を混合し、湿式粉砕機で 5分間粉砕して、水性懸濁状除草組成物を得た  The above ingredients were mixed and pulverized with a wet pulverizer for 5 minutes to obtain an aqueous suspension herbicidal composition.
[0048] 比較例 2 [0048] Comparative Example 2
(1)化合物 A1 (純度 97.9%) 5.0重量部  (1) Compound A1 (Purity 97.9%) 5.0 parts by weight
(2)ベンスルフロンメチル(純度 99.3%) 5.0重量部  (2) Bensulfuron methyl (purity 99.3%) 5.0 parts by weight
(3) Supragil MNS/25 (同前) 4.0重量部  (3) Supragil MNS / 25 (Same as above) 4.0 parts by weight
(4) Rhodorsil 432 (同前) 0.1重量部  (4) Rhodorsil 432 (same as above) 0.1 parts by weight
(5)水 75.9重量部  (5) 75.9 parts by weight of water
(6)キサンタンガム(1.5重量部)及び  (6) Xanthan gum (1.5 parts by weight) and
1,2-ベンズイソチアゾリン- 3-オン(1.0重量部)を含む水 10.0重量部 以上の成分を混合し、湿式粉砕機で 5分間湿式粉砕して、水性懸濁状除草組成物を 得た。  Water containing 1,2-benzisothiazolin-3-one (1.0 part by weight) 10.0 parts by weight or more of the ingredients were mixed, and wet-pulverized for 5 minutes with a wet pulverizer to obtain an aqueous suspension herbicidal composition.
[0049] 比較例 3 [0049] Comparative Example 3
(1)化合物 A1 (純度 97.9%) 5.0重量部  (1) Compound A1 (Purity 97.9%) 5.0 parts by weight
(2)アジムスルフロン(純度 99.0%) 10.0重量部  (2) Azimusulfuron (purity 99.0%) 10.0 parts by weight
(3) Supragil MNS/25 (同前) 4.0重量部 (4) Rhodorsil 432 (同前) 0.1重量部 (3) Supragil MNS / 25 (Same as above) 4.0 parts by weight (4) Rhodorsil 432 (same as above) 0.1 parts by weight
(5)水 70.9重量部  (5) 70.9 parts by weight of water
(6)キサンタンガム(1.5重量部)及び  (6) xanthan gum (1.5 parts by weight) and
1,2-ベンズイソチアゾリン- 3-オン(1.0重量部)を含む水 10.0重量部 以上の成分を混合し、湿式粉砕機で 5分間湿式粉砕して、水性懸濁状除草組成物を 比較例 4  Water containing 1,2-benzisothiazolin-3-one (1.0 part by weight) 10.0 parts by weight The above ingredients were mixed and wet-ground for 5 minutes with a wet pulverizer to produce an aqueous suspension herbicidal composition as Comparative Example 4
(1)化合物 A1 (純度 97.9%) 5.0重量部  (1) Compound A1 (Purity 97.9%) 5.0 parts by weight
(2)アジムスルフロン(純度 99.0%) 15.0重量部  (2) Azimusulfuron (purity 99.0%) 15.0 parts by weight
(3) Supragil MNS/25 (同前) 4.0重量部  (3) Supragil MNS / 25 (Same as above) 4.0 parts by weight
(4) Rhodorsil 432 (同前) 0.1重量部  (4) Rhodorsil 432 (same as above) 0.1 parts by weight
(5)水 75.9重量部  (5) 75.9 parts by weight of water
以上の成分を混合し、湿式粉砕機で 5分間粉砕して、水性懸濁状除草組成物を得た  The above ingredients were mixed and pulverized with a wet pulverizer for 5 minutes to obtain an aqueous suspension herbicidal composition.
[0051] 比較例 5 [0051] Comparative Example 5
(1)化合物 A2 10.0重量部  (1) Compound A2 10.0 parts by weight
(2) Supragil MNS/25 (同前) 4.0重量部  (2) Supragil MNS / 25 (Same as above) 4.0 parts by weight
(3)水 86.0重量部  (3) 86.0 parts by weight of water
以上の成分を混合し、湿式粉砕機で 5分間湿式粉砕して、水性懸濁状除草組成物を 得た。  The above ingredients were mixed and wet pulverized with a wet pulverizer for 5 minutes to obtain an aqueous suspension herbicidal composition.
[0052] 安定性試験例 1  [0052] Stability test example 1
実施例 1及び比較例 1の水性懸濁状除草組成物を、 54 °Cの恒温機中にて 14日間 保存した。経時前後における水性懸濁状除草組成物中の化合物 A1の含量を液体ク 口マトグラフィ一で定量し、その分解率を下記の式にて算出して、経時変化を評価し た。結果を第 1表に示す。  The aqueous suspension herbicidal compositions of Example 1 and Comparative Example 1 were stored in a thermostat at 54 ° C. for 14 days. The content of Compound A1 in the aqueous suspension herbicidal composition before and after aging was quantified by liquid chromatography, and the degradation rate was calculated by the following formula to evaluate the change with time. The results are shown in Table 1.
分解率 (%)=〔 (製造直後の含有量 保存後の含有量) Z製造直後の含有量〕 X 1 00  Decomposition rate (%) = [(Content immediately after production Content after storage) Z Content immediately after production] X 1 00
[0053] [表 1] 第 1表
Figure imgf000018_0001
[0053] [Table 1] Table 1
Figure imgf000018_0001
[0054] 本発明における特定の界面活性剤であるスルホン酸塩類と無機塩とを用いた場合 、当該特定の界面活性剤を単独で用いた場合に比べ、化合物 A1の分解が顕著に 抑制されて 、ることが、上記安定性試験例の結果力もわかる。 [0054] When the sulfonates that are specific surfactants and inorganic salts in the present invention are used, the decomposition of the compound A1 is remarkably suppressed as compared with the case where the specific surfactant is used alone. This also shows the resultant force of the above stability test example.
[0055] 安定性試験例 2  [0055] Stability test example 2
実施例 2及び 3、並びに比較例 2及び 3の水性懸濁状除草組成物を用い、前記安 定性試験例 1と同様にして、経時変化を評価した。結果を、第 2表に示す。なお、実 施例 2又は 3中の他の除草性化合物であるべンスルフロンメチル又はアジムスルフロ ンは安定であった。  Using the aqueous suspension herbicidal compositions of Examples 2 and 3 and Comparative Examples 2 and 3, the time course change was evaluated in the same manner as in the stability test example 1. The results are shown in Table 2. Bensulfuron methyl or azimusulfuron, which are other herbicidal compounds in Example 2 or 3, were stable.
[0056] [表 2] 第 2表
Figure imgf000018_0002
[0056] [Table 2] Table 2
Figure imgf000018_0002
[0057] 本発明における特定の界面活性剤であるスルホン酸塩類と無機塩とを用いた場合 、当該特定の界面活性剤を単独で用いた場合に比べ、化合物 A1の分解が顕著に 抑制されて 、ることが、上記安定性試験例の結果力もわかる。 [0057] When the sulfonates and inorganic salts, which are specific surfactants in the present invention, are used, decomposition of the compound A1 is remarkably suppressed as compared with the case where the specific surfactant is used alone. This also shows the resultant force of the above stability test example.
[0058] 安定性試験例 3  [0058] Stability Test Example 3
実施例 4及び 5、並びに比較例 4及び 5の水性懸濁状除草組成物を用い、前記安 定性試験例 1と同様にして、経時変化を評価した。その結果、実施例 4は比較例 4〖こ 比べ化合物 A1の分解率が低減され、実施例 5は比較例 5に比べ化合物 A2の分解 率が低減された。  Using the aqueous suspension herbic compositions of Examples 4 and 5 and Comparative Examples 4 and 5, the time course change was evaluated in the same manner as in the stability test example 1. As a result, the decomposition rate of Compound A1 was reduced in Example 4 compared to Comparative Example 4 and Example 5 was reduced in Compound A2 compared to Comparative Example 5.
[0059] 生物試験例  [0059] Biological test examples
1/1,000,000 haポットに畑作土壌を詰め、そこへ植物(メヒシバ又はァォゲイトウ)の 種子を播種し、温室内で生育させる。植物力 ¾葉期に達したとき、本発明の水性懸濁 状除草組成物の所定量(100 g a.i./ha)を、 300 L/ha相当の水で希釈し、ここに展 着剤(商品名:サーファタタント WK、花王社製)を加用して、茎葉処理する。処理後 21 日目に植物の生育状態を調査する。その結果、本発明の水性懸濁状除草組成物は 優れた除草活性を示す。 1 / 1,000,000 ha pot is filled with upland soil, plant seeds are planted there, and grown in a greenhouse. When the plant power reaches the ¾ leaf stage, the aqueous suspension of the present invention A predetermined amount (100 g ai / ha) of a herbicidal composition is diluted with water equivalent to 300 L / ha, and a spreading agent (trade name: Surfatatanto WK, manufactured by Kao Corporation) is added here. , Handle the foliage. On the 21st day after treatment, investigate the growth of the plant. As a result, the aqueous suspension herbicidal composition of the present invention exhibits excellent herbicidal activity.
産業上の利用可能性 Industrial applicability
本発明の該水性懸濁状除草組成物は、耕作地における作物保護や非農耕地での 雑草防除に有効に利用される。 なお、 2005年 8月 10曰に出願された曰本特許出願 2005— 231841号、 2005年 11月 10曰に出願された曰本特許出願 2005— 326624号及び 2006年 2月 21曰に 出願された日本特許出願 2006— 044472号の明細書、特許請求の範囲、及び要 約書の全内容をここに引用し、本発明の明細書の開示として、取り入れるものである  The aqueous suspension herbicidal composition of the present invention is effectively used for crop protection in cultivated land and weed control in non-agricultural land. In addition, the Japanese Patent Application 2005- 231841 filed on August 10, 2005, the Japanese Patent Application 2005-326624 filed on November 10, 2005, and the February 21, 2006 application The entire contents of the specification, claims, and summary of Japanese Patent Application No. 2006-044472 are incorporated herein by reference as the disclosure of the specification of the present invention.

Claims

請求の範囲 The scope of the claims
[1] (1) 1— [3— [ (4,6 ジメトキシピリミジン一 2—ィルカルバモイル)スルファモイル]— [1] (1) 1— [3— [(4,6 Dimethoxypyrimidine 2-ylcarbamoyl) sulfamoyl] —
2 ピリジル]—2 フルォロプロピル メトキシアセテート、 N— [(4, 6 ジメトキシピリ ミジン— 2—ィル)ァミノカルボ-ル]— 2— (2—フルオロー 1—ヒドロキシプロピル)2 Pyridyl] —2 Fluoropropyl methoxyacetate, N — [(4, 6 Dimethoxypyrimidine—2-yl) aminocarbol] — 2— (2-Fluoro-1-hydroxypropyl)
3 ピリジンスルホンアミド及びそれらの塩力もなる群力 選ばれた少なくとも 1種の除 草性スルホニルゥレア系化合物、(2)無機塩、(3)ァリールスルホン酸塩、アルキルァ リールスルホン酸塩及びそれらのホルマリン縮合物力もなる群力も選ばれた少なくと も 1種のスルホン酸塩並びに (4)水を含有する水性懸濁状除草組成物。 3 Pyridinesulfonamides and their group strengths that also have salt power At least one selected herbicidal sulfonylurea compound, (2) inorganic salts, (3) arylaryl sulfonates, alkyl aryl sulfonates and their An aqueous suspension herbicidal composition containing at least one sulfonate salt selected from the group power that is also the power of formalin condensate and (4) water.
[2] 除草性スルホ -ルゥレア系化合物が 1 [3— [ (4, 6 ジメトキシピリミジン 2—ィル 力ルバモイル)スルファモイル]— 2—ピリジル]— 2—フルォロプロピル メトキシァセテ ートである、請求項 1に記載の水性懸濁状除草組成物。  [2] The herbicidal sulfo-lurea compound is 1 [3— [(4, 6 dimethoxypyrimidine 2-yl rubamoyl) sulfamoyl] —2-pyridyl] —2-fluoropropyl methoxyacetate. The aqueous suspension herbicidal composition as described.
[3] 無機塩がリン酸塩である、請求項 1に記載の水性懸濁状除草組成物。 [3] The aqueous suspension herbicidal composition according to claim 1, wherein the inorganic salt is a phosphate.
[4] リン酸塩力 リン酸二水素ナトリウム及びリン酸二水素カリウム力 なる群力 選ばれ た少なくとも 1つである、請求項 3に記載の水性懸濁状除草組成物。 [4] The aqueous suspension herbicidal composition according to claim 3, which is at least one selected from the group power consisting of sodium dihydrogen phosphate and potassium dihydrogen phosphate.
[5] リン酸塩がリン酸二水素ナトリウムである、請求項 4に記載の水性懸濁状除草組成 物。 [5] The aqueous suspension herbicidal composition according to claim 4, wherein the phosphate is sodium dihydrogen phosphate.
[6] スルホン酸塩が、アルキルベンゼンスルホン酸塩、アルキルナフタレンスルホン酸 塩、アルキルベンゼンスルホン酸塩ホルマリン縮合物及びアルキルナフタレンスルホ ン酸塩ホルマリン縮合物カゝらなる群カゝら選ばれた少なくとも 1つである、請求項 1に記 載の水性懸濁状除草組成物。  [6] The sulfonate is at least one selected from the group consisting of alkylbenzene sulfonate, alkylnaphthalene sulfonate, alkylbenzene sulfonate formalin condensate and alkyl naphthalene sulfonate formalin condensate. The aqueous suspension herbicidal composition according to claim 1, wherein
[7] スルホン酸塩力 アルキルベンゼンスルホン酸塩ホルマリン縮合物及びアルキルナ フタレンスルホン酸塩ホルマリン縮合物からなる群力 選ばれた少なくとも 1つである[7] Sulfonate power Group power consisting of alkylbenzene sulfonate formalin condensate and alkylnaphthalene sulfonate formalin condensate is at least one selected
、請求項 6に記載の水性懸濁状除草組成物。 The aqueous suspension herbicidal composition according to claim 6.
[8] 更に他の除草性化合物を含有する請求項 1に記載の水性懸濁状除草組成物。 8. The aqueous suspension herbicidal composition according to claim 1, further comprising another herbicidal compound.
[9] 請求項 1に記載の水性懸濁状除草組成物の除草有効量を、望ましくな 、植物又は それが生育する場所に施用することからなる、望ましくない植物を防除又はその生育 を抑制する方法。 [9] Controlling or inhibiting the growth of an undesirable plant comprising applying the herbicidally effective amount of the aqueous suspension herbicidal composition according to claim 1 to a desirable plant or a place where it grows Method.
[10] 無機塩と、ァリールスルホン酸塩、アルキルァリールスルホン酸塩及びそれらのホル マリン縮合物力 なる群力 選ばれた少なくとも 1種のスルホン酸塩とを用いて、水性 懸濁状除草組成物中の 1 [3— [(4,6 ジメトキシピリミジン 2 ィルカルバモイル )スルファモイル] - 2-ピリジル] - 2-フルォロプロピルメトキシアセテート、 N— [ (4 , 6 ジメトキシピリミジン一 2—ィル)ァミノカルボ-ル]— 2— (2 フルォロ一 1—ヒド ロキシプロピル)— 3—ピリジンスルホンアミド及びそれらの塩力 なる群力 選ばれた 少なくとも 1種の除草性スルホニルゥレア系化合物を安定ィ匕させる方法。 [10] Inorganic salts, arylene sulfonates, alkylaryl sulfonates and their forols Marine condensate power Group power 1 [3— [(4,6 Dimethoxypyrimidine 2-ylcarbamoyl) sulfamoyl]-2 in aqueous suspension herbicidal composition with at least one selected sulfonate Pyridyl]-2-fluoropropyl methoxyacetate, N— [(4, 6 Dimethoxypyrimidine 1-yl) aminocarbol] — 2— (2 Fluoro 1-hydroxypropyl) — 3-Pyridinesulfonamide And a method for stabilizing at least one selected herbicidal sulfonylurea compound.
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