JPH0725712A - Herbicidal composition - Google Patents

Abstract

PURPOSE:To obtain a herbicidal composition capable of completely controlling annual gramineous and broad-leaved weeds and perennial weeds at a low dose without exerting the phytotoxicity on agricultural and horticultural crops. CONSTITUTION:This herbicidal composition contains (A) a 1,3-oxazin-4-one derivative expressed by formula I [R is methyl or ethyl; Y is halogen, haloalkyl or haloalkoxy; (n) is 0-3] and (B) at least one selected from 5-tertiary butyl-3-(2,4-dichloro-5-isopropoxyphenyl)-1,3,4-oxadiazol-2-(3H)--one, 2-(2,4-dichloro- m-tolyloxypropionanilide,2-bromo-3,3-dimethyl-N-(1-methyl-1-phenylethyl) butyramide,4'-nitrophenyl-2,4,6--trichlorophenyl ether, 2,4-bis(ethylamino)-6- methylthio-s-triazine and compounds expressed by formulas II to VII in an amount of preferably 0.1-500 pts.wt. based on 1 pt.wt. ingredient (A).

Description

Detailed Description of the Invention

[0001]

FIELD OF THE INVENTION The present invention relates to a herbicidal composition, and more particularly, it contains a combination of a certain 1,3-oxazin-4-one derivative and a known herbicide as an active ingredient. The present invention relates to a herbicidal composition having a wide herbicidal spectrum and capable of exhibiting a sufficient herbicidal effect with a low dose.

[0002]

BACKGROUND OF THE INVENTION Many herbicides have been put to practical use for paddy fields so far.
They are widely and commonly used as a single agent or a mixture containing two or more active ingredients. However, although these agents are relatively effective for annual weeds, their effect on perennial weeds is insufficient, and therefore, in recent years in domestic rice fields, the tendency of increasing perennial weeds with high fertility such as firefly, Urikawa, and Cyperus japonicus has increased. There is a strong need for the development of effective herbicides against these perennial weeds.

The inventors of the present invention have conducted extensive studies to develop a weeding agent satisfying the above-mentioned demands, and as a result, have developed a certain novel 1,3-type previously proposed by the present inventors. Selection of a wide range of weeds in paddy fields by combining an oxazin-4-one derivative (see Japanese Patent Application No. 4-40108) with certain known herbicides having different herbicidal mechanism and spectrum. Of the present invention, the herbicidal efficacy of the herbicides is synergistically increased as compared with the case where each of them is used alone. Therefore, it can be applied at a low dose and the herbicidal spectrum is further expanded, and the present invention is completed. It came to do.

[0004]

Thus, according to the present invention, (A) the following general formula (I)

[0005]

[Chemical 2]

[In the formula, R represents a methyl group or an ethyl group, Y represents a halogen atom, a lower haloalkyl group or a lower haloalkoxy group, and n is 0, 1, 2 or 3. ] At least one 1,3-oxazin-4-one derivative represented by the formula (hereinafter, this may be referred to as "component A"), and (B) 5-tertiarybutyl-3-
(2,4-dichloro-5-isopropoxyphenyl)-
1,3,4-oxadiazole-2- (3H) one, 1,
3-Dimethyl-4- (2,4-dichloro-3-methylbenzoyl) -5- (4-methyl-phenacyloxy) pyrazole, 2- (2,4-dichloro-m-tolyloxy) propionanilide, (RS)- 2-bromo-3,
3-Dimethyl-N- (1-methyl-1-phenylethyl) -3,3-dimethylbutyramide, 2,3-dihydro-3,3-dimethylbenzofuran-5-ylethanesulfonate, 1- (α, α- Dimethylbenzyl) -3-p
-Tolylurea, 1- (2-chlorobenzyl) -3-
(Α, α-Dimethylbenzyl) urea, 4-nitrophenyl 2,4,6-trichlorophenyl ether, methyl 5
-(2,4-Dichlorophenoxy) -2-nitrobenzoate, and 2,4-bis (ethylamino) -6-methylthio-S-triazine 2- (1,2-dimethylpropylamino) -4-ethyl Amino-6-methylthio-1,
Provided is a herbicidal composition comprising at least one compound selected from 3,5-triazine (hereinafter, this may be referred to as "component B") as an active ingredient.

The herbicidal composition of the present invention will be described in more detail below.

The 1,3-oxazin-4-one derivative represented by the above general formula (I), which is used as the component A in the herbicidal composition of the present invention, is a novel compound which has not been published in conventional publications. The details of its production method, physical properties, herbicidal activity and the like are disclosed in Japanese Patent Application No. 4-40108 previously filed.

In the present specification, the term "lower" means that the group or compound to which this term is attached has 6 or less carbon atoms.

In the compound of the above formula (I), the "halogen atom" represented by Y includes four kinds of fluorine, chlorine, bromine and iodine atoms, and the "lower haloalkyl group" is lower alkyl. A group in which at least one of the hydrogen atoms of the group is substituted with a halogen atom, for example, bromomethyl, dichloromethyl, trifluoromethyl, 2
-Iodoethyl, 1-chloroethyl, 3-chloropropyl, 2-methyl-2-chloropropyl, 2,2,2-trifluoroethyl group and the like can be mentioned, and the "lower haloalkoxy group" is a lower alkoxy group. A group in which at least one of hydrogen atoms is substituted with a halogen atom, for example, trifluoromethoxy, difluoromethoxy, chlorodifluoromethoxy, 2-chloroethoxy,
Examples thereof include 1,1,2,2-tetrafluoroethoxy, 3-chloropropoxy, 2,2,3,3,3-pentafluorochloropoxy group and the like.

Representative examples of the compound of the formula (I) are as follows.

No. 1: 6-methyl-3- [1-methyl-
1- (3,5-dichlorophenyl) ethyl] -5-phenyl-2,3-dihydro -4 H-1,3-oxazin-4
- one No.2: 6- methyl-3- [1-methyl-1- (3-chlorophenyl) ethyl] -5-phenyl-2,3-dihydro -4 H-1,3-oxazin-4-one No .3: 6-methyl-3- [1-methyl-1- (3-fluoro-phenylalanine) ethyl] -5-phenyl-2,3-dihydro -4 H-1,3-oxazin-4-one No. 4: 6-methyl-3- [1-methyl-1- (4-fluoro-phenylalanine) ethyl] -5-phenyl-2,3-dihydro -4 H-1,3-oxazin-4-one No.5 : 6-methyl-3- [1-methyl-1- (2-chlorophenyl) ethyl] -5-phenyl-2,3-dihydro -4 H-1,3-oxazin-4-one No.6: 6 Methyl-3- [1-methyl-1- (3-methylphenyl) ethyl] -5-phenyl-2,3-dihydro- H-1,3-oxazin-4-one No.7: 6- methyl-3- [1-methyl-1- (3-difluoromethyl-methoxyphenyl) ethyl] -5-phenyl -
Compounds represented by 2,3-dihydro -4 H-1,3-oxazin-4-one Formula (I) are, for example, can be produced by the method shown in the following reaction formula.

[0013]

[Chemical 3]

[Wherein R, Y and n are as defined above] The reaction of the compound of formula (II) with the compound of formula (III) is carried out in a suitable solvent or without solvent. The reaction temperature can usually be about 90 ° C. to about 160 ° C. or a temperature between the boiling points of the solvents used. The solvent in the case of using a solvent is not particularly limited as long as it is substantially inert to the reaction, but from the viewpoint of the reaction temperature, the boiling point of toluene, xylene, mesitylene, etc. is 90. It is preferable to use an organic solvent having a high boiling point of ℃ or higher. The reaction time varies depending on other reaction conditions used,
Generally, it can be completed in 1 to 120 minutes.

Further, the compound of formula (I
The proportion of the compound of the formula (II) used is not strictly limited, but is usually the formula (II) per mol of the compound of the formula (II).
The compounds of I) are expediently used in a range of 0.5 to 2 mol, in particular 0.9 to 1.1 mol.

Separation and purification of the resulting compound of formula (I) from the reaction mixture can be carried out by a method known per se, for example, recrystallization, extraction, chromatography and the like.

The compound of formula (II) used as a starting material in the above reaction can be prepared by a method known per se, for example,
Chem. Pharm. Bull., 31 (6), 1895-190.
1 (1983), and the compounds of formula (III) are also known per se, eg as described in US Pat. No. 2,571,759. Can be manufactured in.

More specifically, the compound of formula (III) can be prepared, for example, by the following reaction formula

[0019]

[Chemical 4]

It can be prepared by dropping the compound of the formula (V) into formalin according to the formula [wherein Y is as defined above]. The reaction temperature is preferably about room temperature. Although the reaction time varies depending on other reaction conditions, it can usually be completed in about 0.1 to 10 hours. The product of formula (III) can be separated from the reaction mixture by a conventional method, and can be easily purified by recrystallization, distillation, column chromatography and the like.

On the other hand, the following compounds (1) to (10) used as the component (B) of the herbicidal composition of the present invention are commonly used herbicides known per se, and details thereof are, for example: It is described in the publication as follows.

(1) 5-tertiary butyl-3-
(2,4-dichloro-5-isopropoxyphenyl)-
1,3,4-oxadiazole-2- (3H) one

[0023]

[Chemical 5]

See Japanese Patent Publication No. 44-15649.

(Hereinafter, this compound may be referred to as "G-315".) (2) 1,3-Dimethyl-4- (2,4-dichloro-3)
-Methylbenzoyl) -5- (4-methyl-phenacyloxy) pyrazole

[0026]

[Chemical 6]

See JP-A-62-19402.

(Hereinafter, this compound may be referred to as "MY-71".) (3) 2- (2,4-dichloro-5-m-tolyloxy) -propionanilide

[0029]

[Chemical 7]

See JP-A-57-171904.

(Hereinafter, this compound may be referred to as "MY-15".) (4) 2-bromo-3,3-dimethyl-N- (1-methyl-1-phenylethyl) butyramide

[0032]

[Chemical 8]

See US Pat. No. 4,288,244.

(Hereinafter, this compound may be referred to as "S-47".) (5) 2,3-dihydro-3,3-dimethylbenzofuran-5-ylethanesulfonate

[0035]

[Chemical 9]

See Japanese Patent Publication No. 55-45523.

(Hereinafter, this compound may be referred to as "NS-112".) (6) 1- (α, α-dimethylbenzoyl) -3-p
− Torilurea

[0038]

[Chemical 10]

See Japanese Patent Publication No. 48-35454.

(Hereinafter, this compound may be referred to as "SK-23".) (7) 1- (2-chlorobenzyl) -3- (α, α-
Dimethylbenzyl) urea

[0041]

[Chemical 11]

See JP-A-60-172910.

(Hereinafter, this compound may be referred to as "JC-940".) (8) 4'-nitrophenyl 2,4,6-trichlorophenyl ether

[0044]

[Chemical 12]

See British Patent No. 10166648.

(Hereinafter, this compound may be referred to as "CNP".) (9) Methyl 5-2,4 dichlorophenoxy) -2-
Nitrobenzoate

[0047]

[Chemical 13]

See JP-B-48-4609.

(Hereinafter, this compound may be referred to as "MC-79".) (10) 2,4-bis (ethylamino) -6-methylthio-S-triazine

[0050]

[Chemical 14]

See Swiss Patent No. 337019.

(Hereinafter, this compound may be referred to as "G32911") (11) 2- (1,2-dimethylpropylamino)-
4-ethylamino-6-methylthio-1,3,5-triazine

[0053]

[Chemical 15]

See Belgian Patent No. 714992.

(Hereinafter, this compound is referred to as "CG-7103".
The herbicidal composition of the present invention further has the purpose of improving herbicidal activity, expanding target grass species, expanding suitable treatment period, expanding residual effect, and reducing phytotoxicity under adverse conditions. Other herbicides can also be incorporated as appropriate. Examples of other herbicides that can be incorporated include the following compounds.

Phenyloxy 2,4-dichlorophenoxyacetate citrate (generic name: 2,4-D, THE PESTICIDE MANUAL 9th Edition (199
1 year) p218-219), 4- (4-chloro-2)
-Methylphenoxy) butyric acid (generic name: M
CPB, see British Patent No. 758980), 4-
Chloro-2-methylphenoxyacetate (generic name: MCPA, THE PESTICIDE MANUAL 9th edition (1
991) p533), 2- (2-naphthyloxy) propionanilide (generic name: naproanilide, TH
E PESTICIDE MANUAL 9th edition (1991) p610), S-ethyl (4-chloro-2-methylphenoxy) ethanethioate (generic name: MCPA-thioethyl, see US Pat. No. 3,708,278) and the like.

[0057]Diphenyl ether type 2,4-dichlorophenyl 3'-methoxy-4'-nit
Rhophenyl ether (generic name: clomethoxynil (agricultural
Yakuhin Handbook 1989, pp. 500), Acid amide type N-butoxymethyl-2-chloro-2 ', 6'-diethyl
Luacetanilide (generic name: butachlor, US Patent No.
3442945), 2-chloro-2 ',
6'-diethyl-N- (n-propoxyethyl) -acetate
Toanilide (generic name: pretilachlor, JP-A-49-
54527), 2-benzothiazole-2-
Iroxy-N-methyl-acetanilide (generic name: me
(Fenaset, refer to JP-A-54-154762)
etc.

Diazine-based 4- (2,4-dichlorobenzoyl) -1,3-dimethylpyrazol-5- yltoluene- 4-sulfonate (general name: pyrazolate, see JP-A-50-126830), 2- [[4- (2,4-dichlorobenzoyl)
-1,3-Dimethyl-1H-pyrazol-5-yl] oxy] -1-phenylethanone (general name: pyrazoxifene, see British Patent No. 20023375), 3-
Isopropyl-1H-2,1,3-benzothiadiazine-
4 (3H) -one-2,2-dioxide (generic name: bentazone, see US Pat. No. 3,708,277), carbamate S-1-methyl-1-phenylethylpiperidine-1-
Carbothioate (generic name: dimepiperate, JP-A-5
1-98331), methyl (3,4-dichlorophenyl) -capamate (generic name: suep, THE PE
STICIDE MANUAL 9th Edition (1991, p. 927),
S- (4-chlorobenzyl) -diethyl-thiocarbamate (generic name: thiobencarb, JP-B-43-2902)
4), S-ethylhexahydro-1H-azepine-1-carbothioate (generic name: molinate, see U.S. Pat. No. 3,1987,786), S-benzyl 1,2-diethylpropyl (ethyl) thio. Carbamate (generic name: esprocarb, U.S. Pat. No. 3,742,00)
No. 5, specification) etc.

Organophosphorus S-2-methylpiperidinocarbonylmethyl 0,0-dipropyl phosphorodithioate (generic name: piperophos,
Belgian Patent No. 725,992), S-2
-Benzenesulfonylaminoethyl 0.0-diisopropyl phosphorothioate and the like.

The above-mentioned herbicides which can be blended appropriately are referred to as "C
Sometimes called "ingredient".

Further, the herbicidal composition of the present invention may be optionally blended with an insecticide, a fungicide, a plant growth regulator and the like.

In the herbicidal composition of the present invention, the 1,3-oxazin-4-one derivative represented by the formula (I) (component A) and the compounds (1) and (2) (component B) described above. The combination is not particularly limited, but the following combinations are preferable.

Component A: Compound No. 1 and component B: G-31
5, A component: Compound No. 1 and B component: MY-71, A component: Compound No. 1 and B component: SK-23, A component: Compound No. 1 and B component: CNP, A component: Compound No. .1 and B
Component: MC-79, A component: Compound No. 1 and B component: M
Y-71 and S-47, A component: Compound No. 1 and B component: MY-71 and JC-940, A component: Compound N
o.1 and B component: MY-71, MY-15 and S-4
7, A component: Compound No. 1 and B component: MY-71, MY
-15 and NS-112, A component: Compound No. 1 and B
Ingredients: G32911, etc.

Compound No. 1 as the component A is a compound produced in Production Example 1 described later.

In the herbicidal composition of the present invention, the components A and B
The mixing ratio of the components is not strictly limited, and can be varied over a wide range depending on the application site, application target, application period, etc. of the final herbicide composition, but in general, the former A It is suitable to add the latter component B in an amount of 0.05 to 1000 parts by weight, preferably 0.1 to 500 parts by weight, relative to 1 part by weight of the component.

When the C component is further compounded in the above herbicidal composition, the compounding ratio is not strictly limited, and it may be widely varied depending on the application site, application time and the like of the final herbicidal composition. Can be changed.

When the composition of the present invention is actually used as a herbicide, the above-mentioned active ingredient is treated with a solid or liquid carrier or diluent known per se, a surfactant or other auxiliaries for formulation, and a method known per se. It is possible to prepare a formulation form which is usually used as an agricultural chemical, for example, granules, wettable powders, flowable formulations and the like.

Examples of solid carriers that can be used in the production of herbicides include kaolinite group, montmorillonite group,
Clays represented by the illite group and polygloskite group, more specifically, pyrophyllite, attapulgite,
Sepiolite, kaolinite, bentonite, saponite, vermiculite, mica, talc, etc .; gypsum, calcium carbonate, dolomite, diatomaceous earth, calcite, magnesium lime, apatite, zeolite, anhydrous silicic acid, synthetic calcium silicate, etc. Other inorganic substances; soy flour, tobacco flour, walnut flour, wheat flour, wood flour, starch, crystalline cellulose and other plant organic substances; coumarone resin, petroleum resin, alkyd resin, polyvinyl chloride, polyalkylene glycol, ketone resin, ester Examples thereof include synthetic or natural polymer compounds such as gum, cobal gum, and dammal gum; waxes such as carnauba wax and beeswax, and urea.

Suitable liquid carriers include, for example, paraffinic or naphthenic hydrocarbons such as kerosene, mineral oil, spindle oil and white oil; aromatic hydrocarbons such as xylene, ethylbenzene, cumene and methylnaphthalene; trichloroethylene and monochloro. Chlorinated hydrocarbons such as benzene and o-chlorotoluene; ethers such as dioxane and tetrahydrofuran; ketones such as methyl ethyl ketone, diisobutyl ketone, cyclohexanone, acetophenone and isophorone; ethyl acetate, amyl acetate, ethylene glycol acetate, diethylene glycol acetate, Esters such as dibutyl maleate and diethyl succinate; n-hexanol, ethylene glycol, diethylene glycol, cyclohexanol,
Examples thereof include alcohols such as benzyl alcohol; ether alcohols such as ethylene glycol ethyl ether, ethylene glycol phenyl ether, diethylene glycol ethyl ether, and diethylene glycol butyl ether; polar solvents such as dimethylformamide and dimethyl sulfoxide; and water.

In addition, emulsification, dispersion, wetting of the active ingredient,
Surfactants and other auxiliary agents can be used for the purposes of spreading, binding, controlling disintegration, stabilizing active ingredients, improving fluidity, and preventing rust.

Examples of surfactants that can be used include nonionic, anionic, cationic and zwitterionic compounds, but usually nonionic and / or anionic compounds are used. A compound is used.

Suitable nonionic surfactants include, for example, compounds obtained by polymerizing addition of ethylene oxide to higher alcohols such as lauryl alcohol, stearyl alcohol and oleyl alcohol; isooctylphenol,
Compounds obtained by polymerizing addition of ethylene oxide to alkylphenols such as nonylphenol; Compounds obtained by polymerizing addition of ethylene oxide to alkylnaphthols such as butylnaphthol and octylnaphthol; Polymerization addition of ethylene oxide to higher fatty acids such as palmitic acid, stearic acid and oleic acid Compounds; compounds obtained by polymerizing addition of ethylene oxide to amines such as dodecylamine and stearic acid amide; compounds of higher fatty acid esters of polyhydric alcohols such as sorbitan and compounds obtained by polymerizing addition of ethylene oxide; block polymerization addition of ethylene oxide and propylene oxide Examples thereof include compounds.

Suitable anionic surfactants include, for example, alkyl sulphate salts such as sodium lauryl sulphate, oleic alcohol sulphate amine salts; alkyl succinate dioctyl ester sodium, 2-ethylhexene sulphonate sodium and the like. Sulfonates; aryl sulfonates such as sodium isopropylnaphthalenesulfonate, sodium methylenebisnaphthalenesulfonate, sodium ligninsulfonate, and sodium dodecylbenzenesulfonate.

Further, in the composition of the present invention, for the purpose of improving the performance of the preparation and enhancing the herbicidal effect, casein, gelatin, albumin, glue, lignin sulfonate, alginate, gum arabic, carboxymethyl cellulose, Methyl cellulose, hydroxyethyl cellulose,
A high molecular compound such as polyvinyl aldol, polyvinyl pyrrolidone, and polysaccharide may be used together with other auxiliary agents.

The above-mentioned carrier and various auxiliary agents can be appropriately used alone or in combination depending on the purpose in consideration of the dosage form of the preparation, the application scene and the like.

The content of the active ingredient in the composition of the present invention in the various dosage forms thus obtained can be varied depending on the dosage form, but is, for example, 0.01 to 99% by weight, preferably 0.4. It can be in the range of up to 30% by weight.

In the case of a wettable powder, for example, the active ingredient is usually added in an amount of 0.1
The content is 5 to 90% by weight, and the balance is a solid carrier and a dispersion wetting agent, and if necessary, a protective colloid agent, a defoaming agent and the like are added.

In the case of granules, for example, the active ingredient is usually 0.0
It is contained in an amount of 1 to 35% by weight, and the rest is a solid carrier, a surfactant and the like. The active ingredient is either uniformly mixed with the solid carrier, or is fixed or adsorbed uniformly on the surface of the solid carrier, and the particle diameter can be about 0.2 to 1.5 mm.

In the case of a flowable agent, for example, the active ingredient is usually contained in an amount of 0.5 to 50% by weight, the dispersion wetting agent is contained in an amount of 3 to 10% by weight, and the balance is water. A protective colloid agent, an antiseptic agent, an antifoaming agent and the like are added.

The appropriate application amount of the composition of the present invention prepared as described above cannot be unconditionally defined due to differences in meteorological conditions, soil conditions, drug formulation, target crops, target weeds, application time, application method and the like. Usually, it is suitable that the amount is in the range of 0.01 to 10 kg, preferably 0.01 to 2 kg per hectare, based on the total amount of the active ingredients.

If necessary, it can be used by mixing with other various insecticides, fungicides, plant growth regulators, herbicides, fertilizers and other chemicals during spraying.

The herbicidal composition of the present invention is applied to a wide variety of annual weeds such as Nobie, Konagi, Azena, Magnolia japonicus, Firefly, Hiraomodaka and perennial difficult-to-control weeds such as Mizugaya, Kurikawa and Kurowai which occur in paddy fields. It shows a high effect at a low dose, has extremely high safety against paddy rice, and does not cause phytotoxicity which may cause a problem when used normally. In addition, it exerts a high control effect on annual weeds such as Nobie, Mejisoba, Enokurogusa, and perennial difficult-to-control weeds such as nutsedge, which are used in the fields. It can be arbitrarily selected from a wide range of up to about 20 days. Since the herbicidal composition of the present invention can completely control weeds by one treatment, the labor required for weed control can be greatly reduced.

Furthermore, the herbicidal composition of the present invention has a high herbicidal activity of each active ingredient and further has a strong synergistic effect, so that the amount of the active ingredient applied is extremely small as compared with conventional herbicides. I'm sorry. Therefore, the herbicide is highly safe to the environment and farmers, and can be said to be a herbicide that meets the needs of the times.

[0084]

[Examples] Next, production examples, examples and test examples
The invention will be described more specifically. Production example 1 6-methyl-3- [1-methyl-1- (3,
5-dichlorophenyl) ethyl] -5-phenyl-2,
3-dihydro-4H-1,3-oxazin-4-one
Production of (Compound No. 1): Formalin (37% HCHO
Aqueous solution) (4.6 g) was added to 1-methyl-1- (3,5-dioctyl).
Lorophenyl) ethylamine (7.5g) at room temperature
I added it. This was reacted for 7 hours as it was. Reaction mixture
Add saturated sodium bicarbonate solution to the mixture and
Extracted with water, the organic layer was washed with saturated saline, and
Sodium acid was added and dried. Evaporate the solvent under reduced pressure
And white crystals of N-methylene-1-methyl-1- (3.5
8.6 g of -dichlorophenyl) ethylamine were obtained.

Next, 5-phenyl-2,2,6-trimethyl--2 H, 4 H-1,3-dioxin-4-one (0.6
5 g) and N-methylene-1-methyl-1-obtained above.
(3,5-Dichlorophenyl) ethylamine (0.65
The mixture of g) was heated at 150 ° C. for 30 minutes to react.
The reaction mixture was recrystallized from a mixed solvent of hexane and ethyl acetate to give the title compound (0.90 g).

Production Examples 2 to 7 Compounds Nos. 2 to 7 shown in Table 1 below were produced in the same manner as in Production Example 1 above.

Table 1 shows the melting points and ¹ H-NMR peak values of the substances produced by these Production Examples 1 to 7.

[0088]

[Table 1]

Example 1 (Emulsion) Component A: Compound No. 1 0.4% by weight Component B: G-315 8% by weight Polyoxyethylene styrylphenyl ether 3% by weight Calcium dodecylbenzenesulfonate 3% by weight Xylene 85 An emulsion of 0.6% by weight or more was uniformly dissolved.

Example 2 (Wettable powder) Component A: Compound No. 1 0.4% by weight Component B: G-315 8% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulfonate 3% by weight Kaolin 85.6% by weight or more were mixed and pulverized to obtain a wettable powder.

Example 3 (flowable agent) Component A: Compound No. 1 0.4% by weight Component B: MY-71 20% by weight Polyoxyethylene nonylphenyl ether 2% by weight Dioctyl sulfosuccinate sodium 2% by weight Zansan gum 0.2% by weight Water 75.4% by weight The above ingredients were wet pulverized with a wet ball mill to obtain a flowable agent.

Example 4 (Granule) Component A: Compound No. 1 0.13% by weight Component B: MY-71 4% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulfonate 3% by weight Bentonite 30 % By weight Talc 59.87% by weight or more were mixed and pulverized, then granulated by a usual method in a granulator and dried to obtain granules.

Example 5 (Flowable Agent) Component A: Compound No. 1 0.2% by weight Component B: SK-23 20% by weight Polyoxyethylene nonylphenyl ether 2% by weight Dioctyl sulfosuccinate sodium 2% by weight Zansan gum 0.2% by weight Water 75.6% by weight The above ingredients were wet pulverized with a wet ball mill to obtain a flowable agent.

Example 6 (Granule) Component A: Compound No. 1 0.13% by weight Component B: SK-23 6.67% by weight Sodium lignin sulphonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight 30% by weight of bentonite 57.2% by weight of talc were mixed and pulverized, and then granulated by a usual method with a granulator and dried to obtain granules.

Example 7 (Wettable powder) Component A: Compound No. 1 0.4% by weight Component B: CNP 27% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Kaolin 66. At least 6% by weight was mixed and pulverized to obtain a wettable powder.

Example 8 (Granule) Component A: Compound No. 1 0.13% by weight Component B: CNP 9% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulfonate 3% by weight Bentonite 30% by weight Talc 54.87% by weight or more was mixed and pulverized, then granulated by a usual method with a granulator and dried to obtain granules.

Example 9 (Wettable Powder) Component A: Compound No. 1 0.4% by weight Component B: MC-79 20% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulfonate 3% by weight Kaolin 73.6% by weight or more were mixed and pulverized to obtain a wettable powder.

Example 10 (Granule) Component A: Compound No. 1 0.13% by weight Component B: MC-79 6.67% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight 30% by weight of bentonite 57.2% by weight of talc were mixed and pulverized, and then granulated by a usual method with a granulator and dried to obtain granules.

Example 11 (Flowable Agent) Component A: Compound No. 1 0.4% by weight Component B: MY-71 12% by weight Component B: S-47 10% by weight Polyoxyethylene nonylphenyl ether 2% by weight Sodium sulfosuccinate dioctyl ester 2% by weight Zansan gum 0.2% by weight Water 73.4% by weight The above ingredients were wet pulverized with a wet ball mill to obtain a flowable agent.

Example 12 (Granule) Component A: Compound No. 1 0.13% by weight Component B: MY-71 4% by weight Component B: S-47 3.33% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Bentonite 30% by weight Talc 56.54% by weight The above components were mixed and pulverized, then granulated by a usual method in a granulator and dried to obtain granules.

Example 13 (Flowable Agent) Component A: Compound No. 1 0.3% by weight Component B: MY-71 10% by weight Component B: JC-940 10% by weight Polyoxyethylene nonylphenyl ether 2% by weight Sodium sulfosuccinate dioctyl ester 2% by weight Zansan gum 0.2% by weight Water 75.5% by weight The above components were wet pulverized with a wet ball mill to obtain a flowable agent.

Example 14 (Granule) Component A: Compound No. 1 0.1% by weight Component B: MY-71 3.3% by weight Component B: JC-940 3.3% by weight Sodium lignin sulfonate 3 % By weight Sodium dialkylnaphthalene sulphonate 3% by weight Bentonite 30% by weight Talc 57.3% by weight After mixing and pulverizing the above, the mixture was granulated by a usual method in a granulator and dried to obtain granules. .

Example 15 (Flowable Agent) Component A: Compound No. 1 0.4% by weight Component B: MY-71 10% by weight Component B: MY-15 3% by weight Component B: S-47 10% by weight Poly Oxyethylene nonylphenyl ether 2% by weight Sodium sulfosuccinate dioctyl ester 2% by weight Zansan gum 0.2% by weight Water 72.4% by weight The above ingredients were wet-ground with a wet ball mill to obtain a flowable agent.

Example 16 (Granule) Component A: Compound No. 1 0.13% by weight Component B: MY-71 3.33% by weight Component B: MY-15 1% by weight Component B: S-47 3. 34% by weight Sodium lignin sulphonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Bentonite 30% by weight Talc 56.2% by weight After mixing and pulverizing the above, granulate by a usual method with a granulator. Then, it was dried to obtain granules.

Example 17 (Wettable powder) Component A: Compound No. 1 0.4% by weight Component B: MY-71 10% by weight Component B: MY-15 3% by weight Component B: NS-112 4.5 % By weight Sodium lignin sulphonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Kaolin 76.1% by weight The above ingredients were mixed and pulverized to obtain a wettable powder.

Example 18 (Granule) Component A: Compound No. 1 0.13% by weight Component B: MY-71 3.33% by weight Component B: MY-15 1% by weight Component B: NS-112 1. 5% by weight Sodium ligninsulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Bentonite 30% by weight Talc 58.04% by weight After mixing and pulverizing the above, granulate by a usual method with a granulator. Then, it was dried to obtain granules.

Comparative Example 1 (Flowable) Component A: Compound No. 1 0.8% by weight Polyoxyethylene nonylphenyl ether 2% by weight Dioctyl sulfosuccinate sodium 2% by weight Zansan gum 0.2% by weight Water 95% by weight The above was wet-milled with a wet ball mill to obtain a flowable agent.

Comparative Example 2 (Granule) Component A: Compound No. 1 0.27% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Bentonite 30% by weight Talc 63.73% by weight or more After being mixed and pulverized, it was granulated by a usual method with a granulator and dried to obtain granules.

Comparative Example 3 (Emulsion) Component A: Compound No. 1 0.8% by weight Polyoxyethylene styrylphenyl ether 3% by weight Calcium dodecylbenzene sulfonate 3% by weight Xylene 93.2% by weight or more are uniformly dissolved. To obtain an emulsion.

Comparative Example 4 (Flowable Agent) Component B: MY-71 10% by weight Polyoxyethylene nonylphenyl ether 2% by weight Dioctyl ester sodium sulfosuccinate 2% by weight Zansan gum 0.2% by weight water 85.8% by weight The above was wet-milled with a wet ball mill to obtain a flowable agent.

Comparative Example 5 (Granule) Component B: MY-71 4% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Bentonite 30% by weight Talc 60% by weight After mixing and grinding, Granulation was carried out by a usual method using a granulator and dried to obtain granules.

Comparative Example 6 (Flowable Agent) Component B: MY-15 10% by weight Polyoxyethylene nonylphenyl ether 2% by weight Sodium sulfosuccinate dioctyl ester 2% by weight Zansan gum 0.2% by weight Water 85.8% by weight The above was wet-milled with a wet ball mill to obtain a flowable agent.

Comparative Example 7 (Granule) Component B: MY-15 2% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulfonate 3% by weight Bentonite 30% by weight Talc 62% by weight After mixing and pulverizing the above, Granulation was carried out by a usual method using a granulator and dried to obtain granules.

Comparative Example 8 (Flowable Agent) Component B: S-47 10% by weight Polyoxyethylene nonylphenyl ether 2% by weight Dioctyl ester sodium sulfosuccinate 2% by weight Zansan gum 0.2% by weight water 85.8% by weight The above was wet-milled with a wet ball mill to obtain a flowable agent.

Comparative Example 9 (Granule) Component B: S-47 4% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Bentonite 30% by weight Talc 60% by weight After mixing and pulverizing the above, Granulation was carried out by a usual method using a granulator and dried to obtain granules.

Comparative Example 10 (Wettable powder) Component B: NS-112 10% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Kaolin 84% by weight The above components were mixed and pulverized to homogenize water. I got a Japanese medicine.

Comparative Example 11 (Granule) Component B: NS-112 1.5% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Bentonite 30% by weight Talc 62.5% by weight or more After mixing and pulverizing, the mixture was granulated by a usual method with a granulator and dried to obtain granules.

Comparative Example 12 (Flowable Agent) Component B: SK-23 10% by weight Polyoxyethylene nonylphenyl ether 2% by weight Dioctyl sulfosuccinate sodium 2% by weight Zansan gum 0.2% by weight Water 85.8% by weight The above was wet-milled with a wet ball mill to obtain a flowable agent.

Comparative Example 13 (Granule) Component B: SK-23 1.5% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Bentonite 30% by weight Talc 62.5% by weight or more After mixing and pulverizing, the mixture was granulated by a usual method with a granulator and dried to obtain granules.

Comparative Example 14 (Flowable Agent) Component B: JC-940 10% by weight Polyoxyethylene nonylphenyl ether 2% by weight Dioctyl ester sodium sulfosuccinate 2% by weight Zansan gum 0.2% by weight Water 85.8% by weight The above was wet-milled with a wet ball mill to obtain a flowable agent.

Comparative Example 15 (Granule) Component B: JC-940 6% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Bentonite 30% by weight Talc 58% by weight After mixing and grinding, Granulation was carried out by a usual method using a granulator and dried to obtain granules.

Comparative Example 16 (Wettable powder) Component B: CNP 10% by weight Sodium lignin sulphonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Kaolin 84% by weight The above ingredients are mixed and pulverized to obtain a uniform wettable powder. Got

Comparative Example 17 (Granule) Component B: CNP 9% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulfonate 3% by weight Bentonite 30% by weight Talc 55% by weight Granulated by a usual method in a machine and dried to obtain granules.

Comparative Example 18 Component B: MC-79 10% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Kaolin 84% by weight The above ingredients were mixed and pulverized to obtain a wettable powder. .

Comparative Example 19 Component B: MC-79 7% by weight Sodium lignin sulphonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Bentonite 30% by weight Talc 57% by weight After mixing and grinding the above, use a granulator. Then, it was granulated by a usual method and dried to obtain granules.

Comparative Example 20 (Wettable Powder) Component B: MY-71 10% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulfonate 3% by weight Kaolin 84% by weight The above components were mixed and pulverized to homogenize water. I got a Japanese medicine.

Comparative Example 21 (Wettable powder) Component B: MY-15 10% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Kaolin 84% by weight The above components are mixed and pulverized to homogenize water. I got a Japanese medicine.

Comparative Example 22 (Emulsion) Component B: G-315 8% by weight Polyoxyethylene styrylphenyl ether 3% by weight Calcium dodecylbenzenesulfonate 3% by weight Xylene 86% by weight The above ingredients were uniformly dissolved to obtain an emulsion. It was

Comparative Example 23 (Wettable powder) Component B: G-315 8% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Kaolin 86% by weight The above components are mixed and pulverized to homogenize water. I got a Japanese medicine.

Comparative Example 24 (Wettable Powder) Component A: Compound No. 1 1% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Kaolin 93% by weight A wettable powder was obtained.

Comparative Example 25 (Wettable powder) Component B: G32911 4.5% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Kaolin 89.5% by weight A wettable powder was obtained.

Comparative Example 26 (Granule) Component B: G32911 1.5% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Bentonite 30% by weight Talc 62.5% by weight The above were mixed and pulverized. Then, it was granulated by a usual method in a granulator and dried to obtain granules.

Example 19 (Wettable powder) Component A: Compound No. 1 0.4% by weight Component B: G32911 4.5% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Kaolin 89.1% by weight or more were mixed and pulverized to obtain a wettable powder.

Example 20 (Granule) Component A: Compound No. 1 0.13% by weight Component B: G32911 1.5% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Bentonite 30 % By weight Talc 62.37% by weight or more were mixed and pulverized, then granulated by a usual method in a granulator and dried to obtain granules.

Comparative Example 27 (Wettable powder) Component B: CG-7103 3.3% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Kaolin 90.7% by weight The above were mixed and pulverized. To obtain a wettable powder.

Comparative Example 28 (Granule) Component B: CG-7103 1.1% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight Bentonite 30% by weight Talc 62.9% by weight or more After mixing and pulverizing, the mixture was granulated by a usual method with a granulator and dried to obtain granules.

Example 21 (Wettable powder) Component A: Compound No. 1 0.4% by weight Component B: CG-7103 3.3% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight % Kaolin 90.3% by weight or more were mixed and pulverized to obtain a wettable powder.

Example 22 (Granule) Component A: Compound No. 1 0.13% by weight Component B: CG-7103 1.1% by weight Sodium lignin sulfonate 3% by weight Sodium dialkylnaphthalene sulphonate 3% by weight 30% by weight of bentonite, 62.77% by weight of talc and above were mixed and pulverized, then granulated by a usual method with a granulator and dried to obtain granules.

Next, the effects of the herbicidal composition of the present invention will be described with reference to test examples.

Test Example 1 (Pre-Transplantation Treatment) Paddy field soil and chemical fertilizer were put into a Wagner pot having an area of 1 / 5000a, and an appropriate amount of water was added to the mixture to thoroughly stir it to prepare a paddy field, which was prepared in the above Examples and Comparative Examples. The formulations were used to treat the active ingredients shown in Tables 2-10. Two 2-leaf stage paddy rice seedlings, which had been grown in the greenhouse in advance, were transplanted to each plant as 2 strains per pot, and seeds of Novier, Kokonagi, Azena, and Firefly were sown in fixed amounts, and the tubers of Urikawa and Mizugayatsuri were planted. Was planted in a fixed amount, and the water was flooded to a depth of 3 cm.

Thirty days after the chemical treatment, the herbicidal effect on each weed and the degree of phytotoxicity to paddy rice were determined according to the following criteria.

[0142] Herbicidal effect Rice injury about commentary point weeding ratio (%) of about sign-injury 5 100 × withering 4 80 over less than 100 +++ Daigai 3 60 beyond 80 or less ++ in harm 2 40 over 60 below + Minor harm 120 over 40 or less ± Minor harm 0 to 20 or less-harmless The results are shown in Tables 2 to 10 below.

[0143]

[Table 2]

[0144]

[Table 3]

[0145]

[Table 4]

[0146]

[Table 5]

[0147]

[Table 6]

[0148]

[Table 7]

[0149]

[Table 8]

[0150]

[Table 9]

[0151]

[Table 10]

[0152]

[Table 11]

Test Example 2 (Treatment of 1 leaf stage of the fly) Paddy field soil and chemical fertilizer were put into a Wagner pot having an area of 1 / 5000a, and an appropriate amount of water was added thereto, and the mixture was thoroughly stirred to make a paddy field. Two 2-leaf stage paddy rice seedlings, which had been grown in the greenhouse in advance, were transplanted to each plant as 2 strains per pot, and seeds of Novier, Kokonagi, Azena, and Firefly were sown in fixed amounts, and the tubers of Urikawa and Mizugayatsuri were planted. Was planted in a fixed amount, and the water was flooded to a depth of 3 cm.

After the millet was grown in the greenhouse until the 1-leaf stage, using the preparations prepared in the above Examples and Comparative Examples,
The treatment was performed so that the active ingredients shown in Tables 11 to 14 were obtained.

Thirty days after the chemical treatment, the herbicidal effect on each weed and the degree of phytotoxicity to paddy rice were determined according to the criteria of Test Example 1.

The results are shown in Tables 11 to 14 below.

[0157]

[Table 12]

[0158]

[Table 13]

[0159]

[Table 14]

[0160]

[Table 15]

Test Example 3 (Treatment of 2.5 leaf stage of barley) Paddy field soil and chemical fertilizer were put into a Wagner pot having an area of 1 / 5000a, and an appropriate amount of water was added thereto, and the mixture was thoroughly stirred to make a paddy field. Two 2-leaf stage paddy rice seedlings, which had been grown in the greenhouse in advance, were transplanted to each plant as 2 strains per pot, and seeds of Novier, Kokonagi, Azena, and Firefly were sown in fixed amounts, and the tubers of Urikawa and Mizugayatsuri were planted. Was planted in a fixed amount, and the water was flooded to a depth of 3 cm.

After the buds were grown in the greenhouse until the leaf stage reached the 2.5 leaf stage, the active ingredients shown in Tables 15 to 19 were prepared using the preparations prepared in the above Examples and Comparative Examples. Processed.

Thirty days after the chemical treatment, the herbicidal effect on each weed and the degree of phytotoxicity to paddy rice were determined according to the criteria of Test Example 1.

The results are shown in Tables 15 to 19 below.

[0165]

[Table 16]

[0166]

[Table 17]

[0167]

[Table 18]

[0168]

[Table 19]

[0169]

[Table 20]

[0170]

[Table 21]

From the above test results, it was revealed that the herbicidal composition of the present invention can control various weeds with an extremely low dose as compared with the case where each active ingredient is used alone.

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[Procedure amendment]

[Submission date] January 7, 1994

[Procedure Amendment 1]

[Document name to be amended] Statement

[Correction target item name] 0143

[Correction method] Change

[Correction content]

[0143]

[Table 2]

[Procedure Amendment 2]

[Document name to be amended] Statement

[Correction target item name] 0144

[Correction method] Change

[Correction content]

[0144]

[Table 3]

[Procedure 3]

[Document name to be amended] Statement

[Name of item to be corrected] 0145

[Correction method] Change

[Correction content]

[0145]

[Table 4]

[Procedure amendment 4]

[Document name to be amended] Statement

[Name of item to be corrected] 0146

[Correction method] Change

[Correction content]

[0146]

[Table 5]

[Procedure Amendment 5]

[Document name to be amended] Statement

[Correction target item name] 0147

[Correction method] Change

[Correction content]

[0147]

[Table 6]

[Procedure correction 6]

[Document name to be amended] Statement

[Name of item to be corrected] 0148

[Correction method] Change

[Correction content]

[0148]

[Table 7]

[Procedure Amendment 7]

[Document name to be amended] Statement

[Name of item to be corrected] 0149

[Correction method] Change

[Correction content]

[0149]

[Table 8]

[Procedure Amendment 8]

[Document name to be amended] Statement

[Correction target item name] 0150

[Correction method] Change

[Correction content]

[0150]

[Table 9]

[Procedure Amendment 9]

[Document name to be amended] Statement

[Correction target item name] 0151

[Correction method] Change

[Correction content]

[0151]

[Table 10]

[Procedure Amendment 10]

[Document name to be amended] Statement

[Correction target item name] 0152

[Correction method] Change

[Correction content]

[0152]

[Table 11]

[Procedure Amendment 11]

[Document name to be amended] Statement

[Correction target item name] 0157

[Correction method] Change

[Correction content]

[0157]

[Table 12]

[Procedure Amendment 12]

[Document name to be amended] Statement

[Correction target item name] 0158

[Correction method] Change

[Correction content]

[0158]

[Table 13]

[Procedure Amendment 13]

[Document name to be amended] Statement

[Name of item to be corrected] 0159

[Correction method] Change

[Correction content]

[0159]

[Table 14]

[Procedure Amendment 14]

[Document name to be amended] Statement

[Name of item to be corrected] 0160

[Correction method] Change

[Correction content]

[0160]

[Table 15]

[Procedure Amendment 15]

[Document name to be amended] Statement

[Name of item to be corrected] 0165

[Correction method] Change

[Correction content]

[0165]

[Table 16]

[Procedure Amendment 16]

[Document name to be amended] Statement

[Name of item to be corrected] 0166

[Correction method] Change

[Correction content]

[0166]

[Table 17]

[Procedure Amendment 17]

[Document name to be amended] Statement

[Correction target item name] 0167

[Correction method] Change

[Correction content]

[0167]

[Table 18]

[Procedure 18]

[Document name to be amended] Statement

[Name of item to be corrected] 0168

[Correction method] Change

[Correction content]

[0168]

[Table 19]

[Procedure Amendment 19]

[Document name to be amended] Statement

[Name of item to be corrected] 0169

[Correction method] Change

[Correction content]

[0169]

[Table 20]

[Procedure amendment 20]

[Document name to be amended] Statement

[Correction target item name] 0170

[Correction method] Change

[Correction content]

[0170]

[Table 21] ─────────────────────────────────────────────────── ───

[Procedure amendment]

[Submission date] August 8, 1994

[Procedure Amendment 1]

[Document name to be amended] Statement

[Name of item to be corrected] Claim 1

[Correction method] Change

[Correction content]

[Chemical 1] [Wherein R represents a methyl group or an ethyl group, Y represents a halogen atom, a lower haloalkyl group or a lower haloalkoxy group, and n is 0, 1, 2 or 3]. 1,3-oxazin-4-one derivative, and (B) 5-tert-butyl-3- (2,4-dichloro-5-isopropoxyphenyl) -1,3,4-
Oxadiazol-2- (3H) one, 1,3-dimethyl-4- (2,4-dichloro-3-methylbenzoyl) -5- (4-methyl-phenacyloxy) pyrazole, 2- (2,4- Dichloro-m-tolyloxy) propionanilide, 2-bromo-3,3-dimethyl-N- (1-methyl-1)
-Phenylethyl) butyramide, 2,3-dihydro-3,3-dimethylbenzofuran-5
-Ylethanesulfonate, 1- (α, α-dimethylbenzyl) -3-p-tolylurea, 1- (2-chlorobenzyl) -3- (α, α-dimethylbenzyl) urea, 4' -nitrophenyl - 2, 4,6 trickle Rolf enyl ether, methyl 5- (2,4 - dichlorobenzoyl Rolf enoki) -2-
Nitrobenzoate, 2,4-bis (ethylamino) -6-methylthio-S-
Triazine, and 2- (1,2-dimethylpropylamino) -4-ethylamino-6-methylthio-1,3
A herbicidal composition comprising at least one compound selected from 5-triazine as an active ingredient.

[Procedure Amendment 2]

[Document name to be amended] Statement

[Correction target item name] 0006

[Correction method] Change

[Correction content]

[In the formula, R represents a methyl group or an ethyl group, Y represents a halogen atom, a lower haloalkyl group or a lower haloalkoxy group, and n is 0, 1, 2 or 3. ] At least one 1,3-oxazin-4-one derivative represented by the following (hereinafter, this may be referred to as "A component"), and (B) 5-tertiarybutyl-3-
(2,4-dichloro-5-isopropoxyphenyl)-
1,3,4-oxadiazol-2- (3H) one,
1,3-dimethyl-4- (2,4-dichloro-3-methylbenzoyl) -5- (4-methyl-phenacyloxy) pyrazole, 2- (2,4-dichloro-m-tolyloxy) propionanilide, (RS) -2-Bromo-
3,3-Dimethyl-N- (1-methyl-1-phenylethyl) -3,3-dimethylbutyramide, 2,3-dihydro-3,3-dimethylbenzofuran-5-ylethanesulfonate, 1- (α, α-dimethylbenzyl) -3
-P-tolylurea, 1- (2-chlorobenzyl) -3
- (alpha, alpha-dimethylbenzyl) urea, 4 '- nitro <br/> phenyl - 2,4,6 trichloroethane Rolf enyl ether,
Methyl 5- (2,4-dichlorophenoxy) -2-nitrobenzoate, 2,4-bis (ethylamino)-
6-methylthio-S-triazine , and 2- (1,2
-Dimethylpropylamino) -4-ethylamino-6-
Provided is a herbicidal composition comprising at least one compound selected from methylthio-1,3,5-triazine (hereinafter, this may be referred to as "component B") as an active ingredient. It

[Procedure 3]

[Document name to be amended] Statement

[Correction target item name] 0010

[Correction method] Change

[Correction content]

In the compound of the above formula (I), the "halogen atom" represented by Y includes four kinds of fluorine, chlorine, bromine and iodine atoms, and the "lower haloalkyl group" is lower alkyl. A group in which at least one of the hydrogen atoms of the group is substituted with a halogen atom, for example, bromomethyl, dichloromethyl, trifluoromethyl, 2
-Iodoethyl, 1-chloroethyl, 3-chloropropyl, 2-methyl-2-chloropropyl, 2,2,2-trifluoroethyl group and the like can be mentioned, and the "lower haloalkoxy group" is a lower alkoxy group. A group in which at least one of hydrogen atoms is substituted with a halogen atom, for example, trifluoromethoxy, difluoromethoxy, chlorodifluoromethoxy, 2-chloroethoxy,
1,1,2,2-tetrafluoroethoxy, 3-chloropropoxy, mention may be made of 2,2,3,3,3-pentafluoro-pro <br/> epoxy group.

[Procedure amendment 4]

[Document name to be amended] Statement

[Name of item to be corrected] 0015

[Correction method] Change

[Correction content]

Further, the compound of formula (I
The use ratio of the compound of II) to be or not strictly limited, usually, the compound per mole formula of formula (II) (II
The compounds of I) are expediently used in a range of 0.5 to 2 mol, in particular 0.9 to 1.1 mol.

[Procedure Amendment 5]

[Document name to be amended] Statement

[Correction target item name] 0021

[Correction method] Change

[Correction content]

On the other hand, the following compounds (1) to ( 11 ) used as the component (B) of the herbicidal composition of the present invention are commonly used herbicides known per se.
For example, it is described in a publication as follows.

[Procedure correction 6]

[Document name to be amended] Statement

[Correction target item name] 0028

[Correction method] Change

[Correction content]

(Hereinafter, this compound may be referred to as "MY-71".) (3) 2- (2,4-dichloro- m -tolyloxy )
Flop Ropion'anirido

[Procedure Amendment 7]

[Document name to be amended] Statement

[Name of item to be corrected] 0032

[Correction method] Change

[Correction content]

[0032]

[Chemical 8]

[Procedure Amendment 8]

[Document name to be amended] Statement

[Name of item to be corrected] 0037

[Correction method] Change

[Correction content]

[0037] (hereinafter, this compound is sometimes referred to as "NS-112") (6) 1- (α, α- dimethyl-Ben di Le) -3-p-
Trill urea

[Procedure Amendment 9]

[Document name to be amended] Statement

[Correction target item name] 0043

[Correction method] Change

[Correction content]

(Hereinafter, this compound may be referred to as "JC-940".) (8) 4'-nitrophenyl - 2,4,6-trichlorophenyl ether

[Procedure Amendment 10]

[Document name to be amended] Statement

[Correction target item name] 0046

[Correction method] Change

[Correction content]

(Hereinafter, this compound may be referred to as "CNP".) (9) Methyl 5- (2,4 - dichlorophenoxy)
-2-nitrobenzoate

[Procedure Amendment 11]

[Document name to be amended] Statement

[Correction target item name] 0053

[Correction method] Change

[Correction content]

[0053]

[Chemical 15]

[Procedure Amendment 12]

[Document name to be amended] Statement

[Name of item to be corrected] 0057

[Correction method] Change

[Correction content]

Diphenyl ether type 2,4-dichlorophenyl 3'-methoxy-4'-nitro-phenyl ether (generic name: clomethoxynil (see Agricultural Handbook 1989, page 500), acid amide type N-butoxymethyl- 2-chloro-2 ′, 6′-diethylacetanilide (generic name: butachlor, see US Pat. No. 3,442,945), 2-chloro-2 ′,
6'-diethyl-N- (n-propoxyethyl) -acetanilide (generic name: pretilachlor, JP-A-49-
54527), 2-benzothiazole-2-
Iloxy-N-methyl-acetanilide (generic name: mefenacet, see JP-A-54-154762)
etc.

[Procedure Amendment 13]

[Document name to be amended] Statement

[Name of item to be corrected] 0058

[Correction method] Change

[Correction content]

Diazine-based 4- (2,4-dichlorobenzoyl) -1,3-dimethylpyrazol-5- yltoluene- 4-sulfonate (general name: pyrazolate, see JP-A-50-126830), 2- [[4- (2,4-Dichlorobenzoyl) -1,3-dimethyl-1H-pyrazol-5-yl] oxy] -1-phenylethanone (generic name: pyrazoxifene, see British Patent No. 20023275), 3 -Isopropyl-1H-2,1,3-benzothiadiazin-4 (3H) -one-2,2-dioxide (generic name: bentazone, see U.S. Pat. No. 3,708,277), carbamate S-1- Methyl-1-phenylethylpiperidine-1-
Carbothioate (generic name: dimepiperate, JP-A-5
See JP 1-98331), methyl (3,4-dichlorophenyl) - mosquito over Bameto (common name: Suetsupu, T
HE PESTICIDE MANUAL 9th Edition (19
1991) p927), S- (4-chlorobenzyl)
-Diethyl-thiocarbamate (generic name: thiobencarb, see Japanese Patent Publication No. 43-29024), S-ethylhexahydro-1H-azepine-1-carbothioate (generic name: molinate, see U.S. Pat. No. 3,1987,786). ), S-benzyl - 1,2-diethylpropyl (ethyl) thiocarbamate (generic name: esprocarb, see US Pat. No. 3,742,005) and the like.

[Procedure Amendment 14]

[Document name to be amended] Statement

[Correction target item name] 0059

[Correction method] Change

[Correction content]

Organophosphorus S-2-methylpiperidinocarbonylmethyl O, O--
Dipropyl phosphorodithioate (generic name: piperophos, see Belgian Patent No. 725,992), S
2-benzenesulfonylaminoethyl O, O -diisopropylphosphorothioate and the like.

[Procedure Amendment 15]

[Document name to be amended] Statement

[Correction target item name] 0062

[Correction method] Change

[Correction content]

In the herbicidal composition of the present invention, the 1,3-oxazin-4-one derivative represented by the formula (I) (component A) and the compounds (1) to ( 11 ) (component B) described above.
There is no particular restriction on the combination with and, but the following combinations are preferred.

[Procedure Amendment 16]

[Document name to be amended] Statement

[Correction target item name] 0073

[Correction method] Change

[Correction content]

[0073] Suitable anionic surfactants such as sodium lauryl sulfate, alkyl sulfate ester salts such as oleyl alcohol sulfate ester amine salts; dioctylsulfosuccinate sodium, such as sodium 2-ethyl hexenoic acid Alkyl sulfonates: aryl sulfonates such as sodium isopropylnaphthalene sulfonate, sodium methylenebisnaphthalene sulfonate, sodium lignin sulfonate, sodium dodecylbenzene sulfonate, and the like.

[Procedure Amendment 17]

[Document name to be amended] Statement

[Correction target item name] 0143

[Correction method] Change

[Correction content]

[00143]

[Table 2]

[Procedure 18]

[Document name to be amended] Statement

[Correction target item name] 0144

[Correction method] Change

[Correction content]

[0144]

[Table 3]

[Procedure Amendment 19]

[Document name to be amended] Statement

[Name of item to be corrected] 0145

[Correction method] Change

[Correction content]

[0145]

[Table 4]

[Procedure amendment 20]

[Document name to be amended] Statement

[Name of item to be corrected] 0146

[Correction method] Change

[Correction content]

[0146]

[Table 5]

[Procedure correction 21]

[Document name to be amended] Statement

[Correction target item name] 0147

[Correction method] Change

[Correction content]

[0147]

[Table 6]

[Procedure correction 22]

[Document name to be amended] Statement

[Name of item to be corrected] 0148

[Correction method] Change

[Correction content]

[0148]

[Table 7]

[Procedure amendment 23]

[Document name to be amended] Statement

[Name of item to be corrected] 0149

[Correction method] Change

[Correction content]

[0149]

[Table 8]

[Procedure correction 24]

[Document name to be amended] Statement

[Correction target item name] 0150

[Correction method] Change

[Correction content]

[0150]

[Table 9]

[Procedure correction 25]

[Document name to be amended] Statement

[Correction target item name] 0151

[Correction method] Change

[Correction content]

[0151]

[Table 10]

[Procedure Amendment 26]

[Document name to be amended] Statement

[Correction target item name] 0152

[Correction method] Change

[Correction content]

[0152]

[Table 11]

[Procedure Amendment 27]

[Document name to be amended] Statement

[Correction target item name] 0157

[Correction method] Change

[Correction content]

[0157]

[Table 12]

[Procedure correction 28]

[Document name to be amended] Statement

[Correction target item name] 0158

[Correction method] Change

[Correction content]

[0158]

[Table 13]

[Procedure correction 29]

[Document name to be amended] Statement

[Name of item to be corrected] 0159

[Correction method] Change

[Correction content]

[0159]

[Table 14]

[Procedure amendment 30]

[Document name to be amended] Statement

[Name of item to be corrected] 0160

[Correction method] Change

[Correction content]

[0160]

[Table 15]

[Procedure correction 31]

[Document name to be amended] Statement

[Correction target item name] 0162

[Correction method] Change

[Correction content]

After the leaves were grown in the greenhouse until the leaf stage reached the 2.5 leaf stage, the active ingredients shown in Tables 15 to 20 were prepared using the formulations prepared in the above Examples and Comparative Examples. Processed.

[Procedure correction 32]

[Document name to be amended] Statement

[Name of correction target item] 0164

[Correction method] Change

[Correction content]

The results are shown in Tables 15 to 20 below.

[Procedure amendment 33]

[Document name to be amended] Statement

[Name of item to be corrected] 0165

[Correction method] Change

[Correction content]

[0165]

[Table 16]

[Procedure amendment 34]

[Document name to be amended] Statement

[Name of item to be corrected] 0166

[Correction method] Change

[Correction content]

[0166]

[Table 17]

[Procedure amendment 35]

[Document name to be amended] Statement

[Correction target item name] 0167

[Correction method] Change

[Correction content]

[0167]

[Table 18]

[Procedure correction 36]

[Document name to be amended] Statement

[Name of item to be corrected] 0168

[Correction method] Change

[Correction content]

[0168]

[Table 19]

[Procedure amendment 37]

[Document name to be amended] Statement

[Name of item to be corrected] 0169

[Correction method] Change

[Correction content]

[0169]

[Table 20]

[Procedure amendment 38]

[Document name to be amended] Statement

[Correction target item name] 0170

[Correction method] Change

[Correction content]

[0170]

[Table 21]

─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. ⁶ Identification code Internal reference number FI technical display location (A01N 43/86 39:02) (A01N 43/86 43:00) (A01N 43/86 47: 28) (A01N 43/86 33:20) (A01N 43/86 43:64) (72) Inventor Toshiki Maruyama 8-3-1 Chuo, Ami-cho, Inashiki-gun, Ibaraki Sanritsu Yuka Co., Ltd. Tsukuba Research Institute In-house (72) Inventor Yoshihiro Usui 8-3-1 Chuo, Ami-cho, Inashiki-gun, Ibaraki Sanryo Yuka Co., Ltd. Tsukuba Research Institute

Claims (1)

[Claims] 1. (A) The following general formula (I): [Wherein R represents a methyl group or an ethyl group, Y represents a halogen atom, a lower haloalkyl group or a lower haloalkoxy group, and n is 0, 1, 2 or 3]. , 3-Oxazin-4-one derivative and (B) 5-tert-butyl-3- (2,4-
Dichloro-5-isopropoxyphenyl) -1,3,4-
Oxadiazol-2- (3H) one, 1,3-dimethyl-4- (2,4-dichloro-3-methylbenzoyl) -5- (4-methyl-phenacyloxy)
Pyrazole, 2- (2,4-dichloro-m-tolyloxy) propionanilide, 2-bromo-3,3-dimethyl-N- (1-methyl-1)
-Phenylethyl) butyramide, 2,3-dihydro-3,3-dimethylbenzofuran-5-
Ileethanesulfonate, 1- (α, α-dimethylbenzyl) -3-p-tolylurea, 1- (2-chlorobenzyl) -3- (α, α-dimethylbenzyl) urea, 4-nitrophenyl 2,4,6 -Trichlorophenyl ether, methyl 5- (2,4 dichlorophenoxy) -2-nitrobenzoate, and 2,4-bis (ethylamino) -6
-Methylthio-S-triazine, containing at least one compound selected from 2- (1,2-dimethylpropylamino) -4-ethylamino-6-methylthio-1,3,5-triazine as an active ingredient A herbicidal composition comprising: