JP2019182875A - Herbicidal composition - Google Patents

Abstract

To provide a herbicidal composition showing a high herbicidal effect on weeds.SOLUTION: A herbicidal composition contains florpyrauxifen-benzyl, and at least one compound selected from a compound group A consisting of imazosulfuron, propyrisulfuron, and bromobucide.SELECTED DRAWING: None

Description

  The present invention relates to a herbicidal composition.

  Conventionally, many compounds are known as an active ingredient of a herbicide (for example, refer nonpatent literature 1 and 2).

Crop Protection Handbook, vol. 97 (2011) Herbicide Handbook, Ninth edition (2007)

  An object of the present invention is to provide a herbicidal composition that exhibits high herbicidal efficacy against weeds.

As a result of studying to find a herbicidal composition exhibiting high herbicidal efficacy against weeds, the present inventor has found that a composition combining specific herbicides exhibits high herbicidal efficacy against weeds. It came to.
The present invention is as follows.

[1] A herbicidal composition containing fluropyroxifene benzyl and one or more compounds selected from the compound group A consisting of imazosulfuron, propyrisulfuron, and bromobutide.

[2] A method for controlling weeds, the step of spraying a herbicidal composition containing fluropyraloxifene benzyl and one or more compounds selected from the compound group A consisting of propyrisulfuron, imazosulfuron, and bromobutide Alternatively, a method comprising simultaneously spraying a herbicidal composition containing fluropyroxifenebenzyl and a herbicidal composition containing one or more compounds selected from the compound group A.

  The herbicidal composition of the present invention (hereinafter referred to as the present composition) exhibits a synergistic effect and can effectively control a wide range of weeds.

  The composition of the present invention comprises fluorpyraxifen-benzyl (benzoyl 4-amino-3-chloro-6- (4-chloro-2-fluoro-3-methoxyphenyl) -5-fluoropyridine-2-carboxylate) and And one or more compounds selected from Compound Group A consisting of imazosulfuron, propyrisulfuron, and bromobutide.

The composition may further contain one or more compounds selected from the following compound group B in addition to one or more compounds selected from fluropyracoxifene benzyl and compound group A.
Compound group B: 2,3,6-TBA (2,3,6-trichlorobenzoic acid), 2,3,6-TBA dimethylammonium (2,3,6-TBA-dimethylammonium), 2,3,6-TBA Lithium salt (2,3,6-TBA-lithium), 2,3,6-TBA potassium salt (2,3,6-TBA-potassium), 2,3,6-TBA sodium salt (2,3,6) -TBA-sodium), 2,4-D, 2,4-D choline salt (2,4-D choline salt), 2,4-D biproamine (2,4-D biproamine), 2,4-D Doboxyl (2,4-D-doboxyl), 2,4-D 2-ethylhexyl (2,4-D-2-ethylhexyl), 2,4-D 3-butoxy Propyl (2,4-D-3-butoxypropyl), 2,4-D ammonium (2,4-D-ammonium), 2,4-D butyl (2,4-D-butoxyl), 2,4-D Butyl (2,4-D-butyl), 2,4-D diethylammonium (2,4-D-dimethylammonium), 2,4-D dimethylammonium (2,4-D-dimethylammonium), 2,4-D Diolamine salt (2,4-D-diolamine), 2,4-D dodecylammonium (2,4-D-dodecyllamonium), 2,4-D ethyl (2,4-D-ethyl), 2,4- D-heptylammonium (2,4-D-heptyllamonium), 2,4-D-isobutyl (2,4-D-isobu) tyl), 2,4-D isooctyl (2,4-D-isopropyl), 2,4-D isopropyl (2,4-D-isopropyl), 2,4-D isopropylammonium (2,4-D-isopropylammonium) ), 2,4-D lithium salt (2,4-D-lithium), 2,4-D meptyl (2,4-D-methyl), 2,4-D methyl (2,4-D-methyl) 2,4-D octyl (2,4-D-octyl), 2,4-D pentyl (2,4-D-pentyl), 2,4-D propyl (2,4-D-propyl), 2 , 4-D sodium salt (2,4-D-sodium), 2,4-D tefryl (2,4-D-tefuryl), 2,4-D tetradecylammonium (2,4-D-tetradecy) ammonium), 2,4-D triethylammonium (2,4-D-triethylammonium), 2,4-D tris (2-hydroxypropyl) ammonium (2,4-D-tris (2-hydroxypropyl) ammonium), 2 , 4-D-trolamine salt (2,4-D-trolamine), 2,4-DB, 2,4-DB choline salt (2,4-DB choline salt), 2,4-DB biproamine (2,4 -DB-bipromine), 2,4-DBbutyl (2,4-DB-butyl), 2,4-DBdimethylammonium (2,4-DB-dimethylammonium), 2,4-DB isooctyl (2,4- DB-isoctyl), 2,4-DB potassium salt (2,4-DB-po) tasium), 2,4-DB sodium salt (2,4-DB-sodium), acetochlor, acifluorfen, acifluorfen sodium salt, aclonifen, ACN (2-amino-3-chlorophathalene-1,4-dione), alachlor, alidochlor, alloxydim, amethrin, amikacarbazole, amidosulfuron Cyclocyclachlor, aminocycline Pyracrolmethyl (aminocyclopyrchlor-methyl), aminocyclopyrchlor-potassium, aminopyramide, aminopyrido choline salt, aminopyridocholine salt (Aminopyrido-tripromine), amiprophos-methyl, amitrol, anilofos, asuram, atrazine, azafenidini ), Azimsulfuron, beflubutamid, benazolin-ethyl, bencarbazone, benfluralin, sulfuron, sulfuron, sulfuron, sulfuron Bensulide, bentazone, benthicarb, benzfendizone, benzobicyclon, benzofenap, benzthiazron on), bialaphos, bicyclopyrone, bifenox, bispyribac, bispyribac-sodium, bislozone, brocylone, bromocylone, broxylone, Bromophenoxime, bromoxynil, bromoxynyl-octanoate, butachlor, butafenacil, butamifos, butamifinos oxydim), butyrate, caffentrol, carbetaamide, carfentrazone, carfentrazone-ethyl, carfentrazone, clomethoxyphenoxy, clomethoxyben (Chloridazon), chlorimuron, chlorimuron-ethyl, chlorbromulon, chlorotoluron, chloroxuron, chlorpropham, chlorpropham Lorsulfuron, chlorthal-dimethyl, chlorthiamid, cinidon, cinidon-ethyl, cinthylin, cinothurfur, cinthulfuron , Clodinahop-propargyl, clomazone, clomeprop, clopyralid, clopyralido choline salt, clopyralid methyl, clopyralid alipy-methyl), clopyralidoolamine salt (clopyralid-olamine), clopyralid potassium salt (clopyralid-potassium), clopyralid tris (2-hydroxypropyl) ammonium (clopyralid-tris (2-hydroxypropylamine) lanloampramulane, Chloranthrammethyl, cumyluron, cyanazine, cyclopyranyl, cycloate, cyclopyrimorate, cyclosulfamlone, cyclosulfamlone Cloxydim, cyhalofop, cyhalofop-butyl, daimuron, dalapon, dazomet, desmedimate ), Dicamba, dicamba choline salt, dicamba biproamine, dicambabatrolamine, dicamba diglycaamine, dicamiba glycoline salt Ammonium (dicamba) dimethylamine, dicambadiolamine salt (dicamba-diolamine), dicamba-isopropylammonium, dicamba-methylamine, dicambabalamamine potassium, dicambabaolamine salt , Dicamba-sodium, diclobenil, dichlorprop, dichlorprop choline salt, dichlorprop-biproproethyl 2-dipropylamine, Dichlorprop-2-ethylhexyl, dichloroprop-butoxyl, dichloroprop-dimethylammonium, dichloroprop-ethylisomol, dichloro-propyl. Dipropylprop-methyl, dicloprop-P, dicloprop-P choline salt, dicloprop-P-biproamine, dicloprop P 2 Ethylhexyl (dichloroprop-P-2-ethylhexyl), dicloprop-P-dimethylammonium (dichlorprop-P-dimethylammonium), dichlorprop-potassium, diclopropropodi (dichlorprop-fodi) Hopmethyl-, dicloslam, difenoxuron, difenzoquat, difenzoquat methylsulfate, diflufenic, diflufenic Fenzopiru (diflufenzopyr), diflufenzopyr sodium salt (diflufenzopyr-sodium), Jimefuron (dimefuron), dimepiperate (dimepiperate), Jimetakuroru
(Dimethachlor), dimetamethrin (dimetamemid), dimethenamide (dimethenamide-P), dimethylpiperate, dinitramine, dinobide, dinobet ), Diquat dibromide, DSMA (disodium methylarsonate), dithiopyr (dithiopyr), diuron, DNOC (2-methyl-4,6-dinitrophenol), esprocarb (esprocarb) Larin (ethalsulfuron), ethamethsulfuron-methyl, etidimuron, ethofursate, ethoxyphenethyl (ethofursate), ethoxyphenethyl (ethofursate) etbenzanid), fenoxaprop-ethyl, fenoxaprop-ethyl, fenoxaprop-P, fenoxaprop-P-ethyl, fenoxasulf-en e), fenquinotrione, fentrazamide, fenuronide, fenuron, flamprop M (flamprop-M), flazasulfuron, florasulfuram, flazilam fluz (Fluazifop-butyl), fluazifop-P (fluazifop-P), fluazifop-P-butyl, fluazolate, flucarbazone, flucarbazone, flucarbazone flucarbazolone flucetosulfur n), flufenacet, flufenpyr, flufenpyr-ethyl, flumetslam, flumetsulam, flu-microcyl, flu-microcyl ), Flumioxazin, fluometuron, fluoroglycofen-ethyl, fluoxam, flupropanate, flupirsulfuron pyrsulfuron-methyl-sodium), flulenol, fluridone, flurochloridone, fluoxypyryl, fluoxypyroxymethyl, fluoxypyroxymethyl , Flutamon, Fluthiacet, Fluthiacet-methyl, Fomesafen, Fomesafen sodium, Foramsulfuron, Folsulfulfon Glufosinate, glufosinate-ammonium, glufosinate-P, glufosinate P-ammonium, glufosinate-P-sodium, glyphosate-g ), Glyphosate choline salt, glyphosate guanidine derivative salt, glyphosate isopropylamine salt, glyphosate isopropylamine salt iproamine), glyphosate-ammonium salt, glyphosate-diammonium salt, glyphosate-potassium salt, glyphosate-sodium salt, glyphosate-sodium salt Halouxifen, halouxifen-methyl, halosafen, halosulfuron, halosulfuron-methyl, haloxyhop, haloxyhop Haloethoxyhop-ethyl, haloxyhop-methyl, haloxyhop-P-ethoxyl, haloxyhop-P-ethoxyl, haloxyhop-methoxyl ), Imazametabenz, imazametabenz-methyl, imazamox-ammonium salt, imazamic-mmammium, imazamic-mmamon Imazapill (imaza) pyr), imazapyr isopropylammonium salt (imazapyr-isopropylammonium), imazaquine (imazaquin-ammonium), imazapirum umulium (imazaquin-ammonium salt) ), Indanophan, indaziflam, iodosulfuron, iodosulfuron-methyl-sodium, iofensulfuron, iofensulfuron, iofensulfuron ensulfuron-sodium, ioxynil, ioxynil-octanoate, ipfencarbazone, isoproturon, isouron, isoxaben, isoxaben, isoxenol isoxachlortole, isoxaflutole, lactofen, lancotrione sodium salt (lancotrione-sodium), lenacyl, linuron, maleic hydrazide (maleichydrazide) -Chloro-2-meth lphenoxy) acetic acid), MCPA choline salt (MCPA choline salt), MCPA biproamine (MCPA-bipropylamine), MCPA ethyl (MCPA-butylyl), MCPA butyl (MCPA-butoxyl), MCPA butyl (MCPA-MC) (MCPA-dimethylamine), MCPA diolamine salt (MCPA-diolamine), MCPA ethyl (MCPA-ethyl), MCPA isobutyl (MCPA-isobutyl), MCPA-isooctyl (MCPA-isopropyl), MCPA isopropyl (MCPA-isopropyl), MCPA methyl (MCPA-methyl), MCPA Lumine salt (MCPA-olamine), MCPA sodium salt (MCPA-sodium), MCPA-trolamine salt (MCPA-trolamine), MCPB (4- (4-chloro-2-methylphenoxy) butanoic acid), MCPB choline salt (MCPB choline) salt), MCPB biproamine (MCPB-bipromine), MCPB ethyl (MCPB-ethyl), MCPB methyl (MCPB-methyl), MCPB sodium salt (MCPB-sodium), mecoprop (mecoprop choline salt) , Mecoprop BAPMA salt (mecoprop N, N-bis (3-aminopropyl) methylamine salt, mecoprop-biproamine, mecoprop-2-ethylhexyl, mecoprop-dimethylammonium, mecopropdiolamine salt, mecopropdiolamine salt Meloprop-ethadyl, mecoprop-isoctyl, mecoprop-methyl, mecoprop-potassium, mecoprop-sodium, mecoprop-sopromeol Salt coprop-trolamine, mecoprop-P, mecoprop-P choline salt, mecoprop-P 2-ethylhexyl, mecoprop-P-dimethylammonium (mecoprop-P) ), Mecoprop-P-isobutyl, mecoprop-P potassium salt (mecoprop-P-potassium), mefenacet, mesosulfuron, mesosulfuron, metsosulfuron, (Metam , Metamihop, metamitron, metazachlor, metazosulfuron, methazoline, methionol, methionol metolachlor, metsulam, methoxuron, metribuzin, metsulfuron, metsulfuron-methyl, molinate, monolinuron onolinuron), naproanilide (naproanilide), napropamide (napropamide), napropamide M (napropamide-M), naptalam (naptalam), neburon (neburon)
, Nicosulfuron, norflurazon, oleic acid, orbencarb, orthosulfamuron, oryzalin, oxadiaargylzone (Oxasulfuron), oxadichromemephone, oxyfluorfen, paraquat, paraquat-dichloride, pebrate, pelargonic acid (pelargonic acid) endimethalin, penoxslam, pentanochlor, pentoxazone, petoxamid, phenisophan, fenmedifamp, fenmedifamp, fenmedifamp (Pinoxaden), piperophos, pretilachlor, primisulfuron, primisulfuron-methyl, prodiamine, profluzol ol), propoxydim, promethon, promethrin, propachlor, propanil, propaquizafop, propaprof, propaprom, propaprom (Propisochlor), propoxycarbazone, propoxycarbazone sodium salt (propoxycarbazone-sodium), propyrisulfuron, propulamide, roulprop Pyraclonil, pyraflufen-ethyl, pyrasulfoltoyl, pyrazolinoxy (pyrazosulfuron), pyrazosulfoxylpyroxylpyroxy (pyrazulfylpyroxy) ), Piributicalb, pyridafol, pyridate, pyriftalid, pyriminobac, pyriminobac-methyl, pyrimisulfa (Pyrimisulfan), pyrithiobac, pyrithiobac-sodium, pyroxasulfone, pyroxslam, quinclorac, quinclorac, quinclorac, quinclorac, quinclorac, quinclorac, quinclorac, quinclorac. Lohopethyl (quizalofop-ethyl), quizalofop-tefuryl (quizalofop-tefuryl), quizalofop-P (quizalofop-P-ethyl), quizalofop-p-fyl-pizzle Rimsulfuron ron), saflufenacil, cetoxydim, EPTC (S-ethyl N, dipropylcarbamothioate), siduron, simazine, simetriol, simetriol MSMA (sodium hydrogen methylsulfonate), sulcotrione, sulfentrazone, sulfomethuron, sulfomethuron methyl (sulfomethuron), TCA-esulfyl TCA ron), swep, TCA (2,2,2-trichloroacetic acid), tebutam, tebuthiuron, tefuryltrione, tembotrione, tepraloxy (Terbacil), terbumeton, terbuthylazine, terbutryn, tactosmin A, tenylchlor, thiazimine, thiadimine, thiadimine Carbazone-methyl (thiencarbazone-methyl), thifensulfuron, thifensulfuron-methyl, thiafenacyl, thiocarbazyl, tetoflpytoylate (Topramzone), tralkoxydim, triafamon, tri-allate, triasulfuron, triaziflam, tribenuron, tribenuron, tribenuron (Tribenuron-methyl), triclopyr, triclopyr-butyl, triclopyr-ethyl, triclopyr-ethyl, triclopyr-ethyl, triclopyr-ethyl, triclopyr-ethyl, triclopyr-ethylethyl. Trifloxysulfuron, trifloxysulfuron sodium salt (trifluoxysulfuron-sodium), trifludioxazine, trifluralin, triflusulfuron (triflusulfuron) Trifluorosulfuron-methyl, tritosulfuron, vernarate, Ethyl [(3- {2-chloro-4-fluoro-5- [3-methyl-4- (trifluoromethyl) -2, 6-dioxo-1,2,3,6-tetrahydropyrimidin-1-yl] phenoxy} pyridin-2-yl) oxy] acetate (353292-31-6).

Of the compound group B, compounds suitable for the composition of the present invention are not limited, and examples thereof include the following compound group C.
Compound group C: ipfencarbazone, indanophan, oxadichromemephone, cavenstrol, cyclopyranyl, tetoflupyrrolemeth, pyraclonyl, pyrazolinate, phenoxasulfone, phentolazamide, benzobicyclon, pentoxazone, mefenacet, carfentrazone ethyl, cumyllon, chromep Dimethatrine, diemron, tefryltrione, pyrazoxifene, fenquinotrione, benzophenap, benfrate, mesotrione, lancotrione sodium salt

  The compound constituting the compound group A, the compound constituting the compound group B, and fluropyroxifene benzyl are described in Crop Protection Handbook, vol. 97 (2011), http: // www. alanwood. net / pesticides /, or US Pat. No. 6,537,948, which can be produced by known production methods.

  In the present invention, the compound selected from the compound group A, the compound selected from the compound group B, and fluropyroxifene benzyl are forms that can be taken by general agricultural chemicals, that is, the compound is dissolved or dispersed in an appropriate liquid carrier. Or mixed with an appropriate solid carrier or adsorbed on a solid carrier, and formulated into a preparation such as an emulsion, a wettable powder, a flowable agent, a dry flowable agent, and a granule. These preparations may further contain an emulsifier, a dispersing agent, a spreading agent, a penetrating agent, a wetting agent, a mucilage agent, a stabilizer and the like, if necessary, and can be prepared by a method known per se.

  Examples of the liquid carrier (solvent) that can be used in formulating the compound selected from the compound group A, the compound selected from the compound group B, and fluropyroxifene benzyl include water, alcohols (eg, methanol) , Ethanol, 1-propanol, 2-propanol, etherene glycol, etc.), ketones (eg, acetone, methyl ethyl ketone, etc.), ethers (eg, dioxane, tetrahydrofuran, ethylene glycol monomethyl ether, diethylene glycol monomethyl ether, propylene glycol monomethyl ether) Etc.), aliphatic hydrocarbons (eg kerosene, fuel oil, machine oil, etc.), aromatic hydrocarbons (eg benzene, toluene, xylene, solvent naphtha, methylnaphthalene, etc.), halogenated hydrocarbons (eg , Dichloromethane Chloroform, carbon tetrachloride, etc.), acid amides (eg, dimethylformamide, dimethylacetamide, etc.), esters (eg, ethyl acetate, butyl acetate, fatty acid glycerin ester, etc.), nitriles (eg, acetonitrile, propio) Nitriles) and the like. These may be used alone or in combination of two or more in an appropriate ratio. Solid carriers (dilution / extension agents) include vegetable powders (eg, soybean powder, tobacco powder, wheat flour, wood powder, etc.), mineral powders (eg, kaolin, bentonite, acid clay, clays such as clay, talc Talc such as powder, wax stone powder, silica such as diatomaceous earth, mica powder, etc.), alumina, sulfur powder, activated carbon, and the like. These may be used alone or in combination of two or more in an appropriate ratio. Also good. The liquid carrier or solid carrier is usually used in an amount of about 1 to 99% by weight, preferably about 1 to 80% by weight, based on the whole preparation.

  As a surfactant that can be used as an emulsifier, a spreading agent, a penetrating agent, a dispersing agent, etc. in formulating a compound selected from the compound group A, a compound selected from the compound group B, and fluropyroxifene benzyl. For example, soaps, polyoxyethylene alkylaryl ethers (eg, Neugen, AA 142; manufactured by Daiichi Kogyo Seiyaku Co., Ltd.), polyoxyethylene aryl esters (eg, nonal; manufactured by Toho Chemical Co., Ltd.) Alkyl sulfates (eg, Yumar 10, Yumar 40; manufactured by Kao Corporation), alkylbenzene sulfonates (eg, Neogen, Neogen T; manufactured by Daiichi Kogyo Seiyaku Co., Ltd., Neoperex; manufactured by Kao Corporation) , Polyethylene glycol ethers (eg, Nonipol 85, Nonipol 100, Nonipol 160; manufactured by Sanyo Chemical Co., Ltd.), polyvalent alcohol Ruesuteru acids (e.g., Tween 20, Tween 80, manufactured by Kao Corporation) nonionic and anionic surfactants or the like. The surfactant can be used usually in an amount of about 0.1 to about 50% by weight, preferably about 0.1 to 25% by weight, based on the whole preparation.

  In the composition of the present invention, the content of one or more compounds selected from the compound group A, one or more compounds selected from the compound group B, and fluropyroxifenebenzyl is usually about 0.01 to 90% by weight. It is.

  In the present invention, the use amount of one or more compounds selected from the compound group A, one or more compounds selected from the compound group B, and fluropyroxifene benzyl depends on the application scene, application time, application method, and target weeds. Although it is different, it is usually about 5 to 4000 g, preferably about 10 to 2000 g, more preferably about 20 to 1000 g per hectare.

  When the composition of the present invention is a composition containing fluropyroxifene benzyl and one or more compounds selected from the compound group A, one or more compounds selected from florpyroxifene benzyl and the compound group A The mixing ratio is in the range of 1: 0.001 to 1: 2000.

  When the composition of the present invention is a composition containing fluropyroxifene benzyl, one or more compounds selected from the compound group A, and one or more compounds selected from the compound group B, The mixing ratio of xifenebenzyl and one or more compounds selected from the compound group A is in the range of 1: 0.001 to 1: 2000, and is selected from fluropyroxifenebenzyl and the compound group B. The mixing ratio with one or more compounds is in the range of 1: 0.001 to 1: 2000.

  When the composition of the present invention is a composition containing fluropyroxifene benzyl and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50 by weight. The range is preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 by weight ratio. The range is 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl and bromobutide, the mixing ratio of fluropyroxifene benzyl and bromobutide is 1: 0.2 to 1: 500 by weight ratio. The range is preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, imazosulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1: 50, preferably in the range of 1: 0.1 to 1:10, more preferably in the range of 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and bromobutide is by weight, The range is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0. The range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and bromobutide is The weight ratio is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is 1: It is in the range of 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0.03 to 1: 75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadiclomephone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and oxadiclomephone is 1: 0.02 to 1: 50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is by weight, The range is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is from 1: 0.05 to 1: 100, preferably in the range of 1: 0.25 to 1:20, more preferably in the range of 1: 0.5 to 1:10, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is by weight, The range is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0.02 to 1: 50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is by weight, The range is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is 1: It is in the range of 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyracuronyl, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is from 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is expressed by weight ratio, The range is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriftalide, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriftalide is 1: 0.03 to 1: 80, preferably in the range of 1: 0.15 to 1:16, more preferably in the range of 1: 0.3 to 1: 8, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is by weight, The range is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriminobac-methyl and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriminobac-methyl is 1: It is in the range of 0.01 to 1:30, preferably 1: 0.05 to 1: 6, more preferably 1: 0.1 to 1: 3, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is 1: 0. 04-1: 100, preferably 1: 0.2-1: 20, more preferably 1: 0.4-1: 10, and the mixing ratio of fluropyroxifenebenzyl and imazosulfuron is The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and fentrazamide is 1: 0.1 to 1: 150, preferably in the range of 1: 0.5 to 1:30, more preferably in the range of 1: 1 to 1:15, and the mixing ratio of fluropyroxifenebenzyl and imazosulfuron is 1: It is in the range of 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, penoxsulam, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and penoxsulam is from 1: 0.01 to 1: 20, preferably in the range of 1: 0.05 to 1: 4, more preferably in the range of 1: 0.1 to 1: 2, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is by weight, The range is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is from 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is expressed by weight ratio, The range is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0.2 to 1: 500, preferably in the range of 1: 1 to 1: 100, more preferably in the range of 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0. The range is 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is by weight, The range is from 1: 0.06 to 1: 150, preferably from 1: 0.3 to 1:30, more preferably from 1: 0.6 to 1:15, and fluropyroxifenebenzyl and propyrisulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0.03 by weight ratio. It is in the range of 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and the mixing ratio of fluropyroxyphenebenzyl and propyrisulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadiclomephone, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and oxadiclomephone is 1: 0.02 by weight ratio. It is in the range of 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is in a weight ratio of 1: 0.05 to It is in the range of 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, and the mixing ratio of fluropyroxyphenebenzyl and propyrisulfuron is The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0.02 by weight ratio. It is in the range of 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is by weight, The range is from 1: 0.03 to 1:80, preferably from 1: 0.15 to 1:16, more preferably from 1: 0.3 to 1: 8, and fluropyroxifenebenzyl and propyrisulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyracuronyl, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pyracuronyl is 1: 0.04 to It is in the range of 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxyphenebenzyl and propyrisulfuron is The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyrazolinate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pyrazolinate is 1: 0.6 to 1: 1500, preferably 1: 3 to 1: 300, more preferably 1: 6 to 1: 150, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is expressed by weight ratio. The range is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is 1: It is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and it is also possible that fluoropyruoxifenebenzyl and propyrisulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0.1 by weight ratio. 1: 150, preferably in the range of 1: 0.5 to 1:30, more preferably in the range of 1: 1 to 1:15, and the mixing ratio of fluropyroxyphenebenzyl and propyrisulfuron is in a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, benzobicyclon, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and benzobicyclone is 1: It is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and it is also possible that fluoropyruoxifenebenzyl and propyrisulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is in a weight ratio of 1: 0.04 to It is in the range of 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxyphenebenzyl and propyrisulfuron is The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is by weight, The range is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, carfentrazone ethyl, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and carfentrazone ethyl is a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl and pro The mixing ratio with pyrisulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight. .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cumyluron, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and cumyluron is 1: 0.3 to 1: 800, preferably 1: 1.5 to 1: 160, more preferably 1: 3 to 1:80, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is in a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, chromeprop, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and clomeprop is 1: 0.1 by weight ratio. 1: 200, preferably 1: 0.5 to 1:40, more preferably 1: 1 to 1:20, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is in a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyrimoleate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyrimoleate is by weight, The range is from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15, and it is also possible that fluoropyraloxifenebenzyl and propyrisulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, dimethatrine, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and dimethatrine is from 1: 0.01 to 1 by weight. The ratio is 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and the mixing ratio of fluropyroxifenebenzyl and propyrisulfuron is as follows: The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, diimron, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and diimron is 1: 0.1 by weight ratio. The range is 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25. The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is in a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxyphenebenzyl, tefryltrione, and propyrisulfuron, the mixing ratio of fluropyroxifenebenzyl and tefryltrione is 1: It is in the range of 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyrazoxifene, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pyrazoxifene is 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is by weight, The range is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxyphenebenzyl, fenquinotrione, and propyrisulfuron, the mixing ratio of fluropyroxifenebenzyl and fenquinotrione is 1: It is in the range of 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, benzophenap and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and benzophenap is 1: The range is from 0.2 to 1: 400, preferably from 1: 1 to 1:80, more preferably from 1: 2 to 1:40, and the mixing ratio of fluropyroxyphenebenzyl and propyrisulfuron is as follows: The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, benfrate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and benfresate is 1: 0.1 by weight. 1: 300, preferably 1: 0.5 to 1:60, more preferably 1: 1 to 1:30, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is in a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mesotrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and mesotrione is 1: 0.02 by weight ratio. It is in the range of 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, lancotrione sodium salt, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and lancotrione sodium salt is by weight, The range is from 1: 0.05 to 1: 100, preferably from 1: 0.25 to 1:20, more preferably from 1: 0.5 to 1:10, and fluropyroxifenebenzyl and propyrisulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, and bromobutide, the mixing ratio of fluropyroxifenebenzyl and ipfencarbazone is 1: It is in the range of 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and the mixing ratio of fluropyroxifene benzyl and bromobutide Is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50 by weight.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, and bromobutide, the mixing ratio of fluropyroxifene benzyl and indanophan is from 1: 0.03 to 1: 75, preferably in the range of 1: 0.15 to 1:15, more preferably in the range of 1: 0.3 to 1: 7.5, and the mixing ratio of fluropyroxifene benzyl and bromobutide is a weight ratio. In the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadiclomephone, and bromobutide, the mixing ratio of fluropyroxifene benzyl and oxadiclomephone is 1: 0.02 to 1: 50, preferably in the range of 1: 0.1 to 1:10, more preferably in the range of 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and bromobutide is by weight, The range is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, and bromobutide, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: 0.05 to 1: 100, preferably in the range of 1: 0.25 to 1:20, more preferably in the range of 1: 0.5 to 1:10, and the mixing ratio of fluropyroxifene benzyl and bromobutide is, by weight ratio, The range is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, and bromobutide, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0.02 to 1: 50, preferably in the range of 1: 0.1 to 1:10, more preferably in the range of 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and bromobutide is by weight, The range is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, and bromobutide, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is 1: It is in the range of 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and the mixing ratio of fluropyroxifene benzyl and bromobutide Is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50 by weight.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyracuronyl, and bromobutide, the mixing ratio of fluropyroxifene benzyl and pyracuronil is 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and bromobutide is by weight, The range is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriftalide, and bromobutide, the mixing ratio of fluropyroxifene benzyl and pyriftalide is 1: 0.03 to 1: 80, preferably in the range of 1: 0.15 to 1:16, more preferably in the range of 1: 0.3 to 1: 8, and the mixing ratio of fluropyroxifene benzyl and bromobutide is, by weight ratio, The range is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriminobacmethyl, and bromobutide, the mixing ratio of fluropyroxifene benzyl and pyriminobacmethyl is 1: It is in the range of 0.01 to 1:30, preferably 1: 0.05 to 1: 6, more preferably 1: 0.1 to 1: 3, and the mixing ratio of fluropyroxifene benzyl and bromobutide Is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50 by weight.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, and bromobutide, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is 1: 0. The range is from 04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifenebenzyl and bromobutide is: The weight ratio is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, and bromobutide, the mixing ratio of fluropyroxifene benzyl and fentrazamide is 1: 0.1 to 1: 150, preferably in the range of 1: 0.5 to 1:30, more preferably in the range of 1: 1 to 1:15, and the mixing ratio of fluropyroxifene benzyl and bromobutide is 1: The range is 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, penoxthram, and bromobutide, the mixing ratio of fluropyroxifene benzyl and penoxthram is 1: 0.01 to 1: by weight. 20, preferably in the range of 1: 0.05 to 1: 4, more preferably in the range of 1: 0.1 to 1: 2, and the mixing ratio of fluropyroxifene benzyl and bromobutide is, by weight, The range is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, and bromobutide, the mixing ratio of fluropyroxifene benzyl and pentoxazone is from 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and bromobutide is by weight, The range is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, and bromobutide, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0.2 to 1: 500, preferably in the range of 1: 1 to 1: 100, more preferably in the range of 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and bromobutide is 1: 0. The range is from 2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, imazosulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is by weight, It is in the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and it is also possible that fluoropyraloxifenebenzyl and imazosulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The mixing ratio of piroxifene benzyl and bromobutide is 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50 by weight. It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, imazosulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0.03 by weight ratio. It is in the range of 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl. And bromobutide are mixed in a weight ratio of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromephone, imazosulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0.02 by weight ratio. 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is in a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl and bromobutide The mixing ratio by weight is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50. .

When the composition of the present invention is a composition containing fluropyraloxifene benzyl, caffeotrol, imazosulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and caffentrol is in a weight ratio of 1: 0.05 to It is in the range of 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl and bromobutide And the mixing ratio by weight is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, imazosulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0.02 by weight ratio. 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is in a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl and bromobutide The mixing ratio by weight is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, imazosulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is by weight, It is in the range of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and it is also possible that fluoropyraloxifenebenzyl and imazosulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The mixing ratio of piroxifene benzyl and bromobutide is in a weight ratio of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyraclonyl, imazosulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and pyraclonil is from 1: 0.04 to The ratio of 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is the weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl and bromobutide The mixing ratio by weight is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriftalide, imazosulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and pyriftalide is 1: 0.03 by weight ratio. It is in the range of 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl and bromobutide The mixing ratio by weight is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriminobacmethyl, imazosulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and pyriminobacmethyl is a weight ratio, It is in the range of 1: 0.01 to 1:30, preferably 1: 0.05 to 1: 6, more preferably 1: 0.1 to 1: 3, and it is also possible that fluoropyraloxifenebenzyl and imazosulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The mixing ratio of piroxifene benzyl and bromobutide is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50 by weight. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, imazosulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is 1: It is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifenebenzyl and imazosulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. The mixing ratio of phenbenzyl and bromobutide is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50 by weight. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, imazosulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0.1 by weight ratio. The ratio of 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is by weight, It is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and it is also possible that fluoropyraloxifene benzyl and bromobutide The mixing ratio by weight is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, penoxsulam, imazosulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and penoxsulam is 1: 0.01 to 1 by weight. The ratio of 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl and bromobutide The mixing ratio by weight is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, imazosulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and pentoxazone is in a weight ratio of 1: 0.04 to The ratio of 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is the weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl and bromobutide The mixing ratio by weight is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, imazosulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0.2 to The range is 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50. The mixing ratio of fluropyroxifenebenzyl and imazosulfuron is 1: It is in the range of 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and bromobutide Is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50 by weight.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is a weight ratio. In the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and fluoropyraoxifenebenzyl and pro The mixing ratio with pyrisulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. In addition, the mixing ratio of fluropyroxifene benzyl and bromobutide is 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1: 5 by weight. It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0. It is in the range of 03 to 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and it is also possible that fluoropyraloxifenebenzyl and propyrisulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The mixing ratio of piroxifenebenzyl and bromobutide is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50 by weight. That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromefone, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0. It is in the range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. The mixing ratio of phenbenzyl and bromobutide is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50 by weight. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffeotrol, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: 0. The range is from 05 to 1: 100, preferably from 1: 0.25 to 1:20, more preferably from 1: 0.5 to 1:10, and the mixing ratio of fluropyroxifenebenzyl and propyrisulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. The mixing ratio of phenbenzyl and bromobutide is, by weight, 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0. It is in the range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. The mixing ratio of phenbenzyl and bromobutide is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50 by weight.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is a weight ratio. In the range of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and fluoropyroxifenebenzyl and pro The mixing ratio with pyrisulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. The mixing ratio of fluropyroxifene benzyl and bromobutide is in a weight ratio of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyraclonyl, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and pyraclonil is 1: 0. It is in the range of 04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. The mixing ratio of phenbenzyl and bromobutide is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50 by weight.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyrazolinate, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and pyrazolinate is 1: 0. It is in the range of 6 to 1: 1500, preferably 1: 3 to 1: 300, more preferably 1: 6 to 1: 150, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl and bromobutide The mixing ratio by weight is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is in a weight ratio, The range is from 1: 0.04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10, and fluropyroxifenebenzyl and propyrisulfuron. And the mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and The mixing ratio of fluropyroxifene benzyl and bromobutide is 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50 by weight. It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0. The ratio is from 1: 1 to 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15, and the mixing ratio of fluropyroxyphenebenzyl and propyrisulfuron is as follows: The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl. And bromobutide are mixed in a weight ratio of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, benzobicyclone, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and benzobicyclon is in a weight ratio, The range is from 1: 0.04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10, and fluropyroxifenebenzyl and propyrisulfuron. And the mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and The mixing ratio of fluropyroxifene benzyl and bromobutide is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50 by weight. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1: 0. It is in the range of 04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. The mixing ratio of phenbenzyl and bromobutide is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50 by weight. .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0. 2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl and bromobutide The mixing ratio by weight is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, carfentrazone ethyl, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and carfentrazone ethyl is: The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. In addition, the mixing ratio of fluropyroxifene benzyl and bromobutide is 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1 in weight ratio. It is in the range of 50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cumyluron, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and cumyluron is 1: 0. It is in the range of 3 to 1: 800, preferably 1: 1.5 to 1: 160, more preferably 1: 3 to 1:80, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl. And bromobutide are mixed in a weight ratio of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, chromeprop, propylsulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and chromeprop is 1: 0. The range is from 1: 1 to 200, preferably from 1: 0.5 to 1:40, more preferably from 1: 1 to 1:20, and the mixing ratio of fluropyroxyphenebenzyl and propyrisulfuron is as follows: The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl. And bromobutide are mixed in a weight ratio of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyrimoleate, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and cyclopyrimoleate is a weight ratio. In the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15, and fluropyroxifenebenzyl and propyrisulfuron. And the mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and The mixing ratio of fluropyroxifene benzyl and bromobutide is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50 by weight. so That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, dimethatrine, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and dimethatrine is 1: 0. It is in the range of 01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. The mixing ratio of phenbenzyl and bromobutide is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50 by weight.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, diimron, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and diimron is 1: 0. The range is from 1: 1 to 250, preferably from 1: 0.5 to 1:50, more preferably from 1: 1 to 1:25, and the mixing ratio of fluropyroxyphenebenzyl and propyrisulfuron is as follows: The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl. And bromobutide are mixed in a weight ratio of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tefryltrione, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and tefryltrione is by weight, The range is from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15, and it is also possible that fluoropyraloxifenebenzyl and propyrisulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The mixing ratio of piroxifenebenzyl and bromobutide is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, by weight.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyrazoxifene, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and pyrazoxifene is 1: 0. 2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl and bromobutide The mixing ratio by weight is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fenquinotrione, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and fenquinotrione is expressed by weight ratio, The range is from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15, and it is also possible that fluoropyraloxifenebenzyl and propyrisulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The mixing ratio of piroxifenebenzyl and bromobutide is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50 by weight. That.

When the composition of the present invention is a composition containing fluropyraloxifene benzyl, benzophenap, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and benzophenap is a weight ratio, The range is from 1: 0.2 to 1: 400, preferably from 1: 1 to 1:80, more preferably from 1: 2 to 1:40, and the mixing ratio of fluropyroxyphenebenzyl and propyrisulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. The mixing ratio of phenbenzyl and bromobutide is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50 by weight.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, benfrate, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and benfrate is 1: 0. The range is from 1: 1 to 300, preferably from 1: 0.5 to 1:60, more preferably from 1: 1 to 1:30, and the mixing ratio of fluropyroxyphenebenzyl and propyrisulfuron is as follows: The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl. And bromobutide are mixed in a weight ratio of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mesotrione, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and mesotrione is 1: 0. It is in the range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and propyrisulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. The mixing ratio of phenbenzyl and bromobutide is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50 by weight.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, lancotrione sodium salt, propyrisulfuron, and bromobutide, the mixing ratio of fluropyroxifene benzyl and lancotrione sodium salt is a weight ratio. In the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, and fluoropyraoxifenebenzyl and pro The mixing ratio with pyrisulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. In addition, the mixing ratio of fluropyroxifene benzyl and bromobutide is 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably, by weight. : 2 to 1: in the range of 50.

When the composition of the present invention is a composition containing fluropyroxifenebenzyl, ipfencarbazone, carfentrazone ethyl, and imazosulfuron, the mixing ratio of fluropyroxifenebenzyl and ipfencarbazone is: The weight ratio is in the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and fluropyroxifenebenzyl. And carfentrazone ethyl are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The mixing ratio of fluropyroxifene benzyl and imazosulfuron is from 1: 0.02 to 1:50, preferably from 1: 0.1 to 1:10, more preferably by weight. It is properly 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, carfentrazone ethyl, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: It is in the range of 0.03 to 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and fluropyroxifene benzyl and carfentra The mixing ratio with zonethyl is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1 by weight. 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromemephone, carfentrazone ethyl, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: It is in the range of 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifene benzyl and carfentrazone ethyl And the mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and The mixing ratio of fluropyroxifene benzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably : 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, carfentrazone ethyl, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: It is in the range of 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, and fluropyroxifene benzyl and carfentrazone ethyl. And the mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably by weight. Ku is 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, carfentrazone ethyl, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: It is in the range of 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifene benzyl and carfentrazone ethyl And the mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and The mixing ratio of fluropyroxifenebenzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0. To 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, carfentrazone ethyl, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is: The weight ratio is in the range of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and fluropyroxifene benzyl. And carfentrazone ethyl are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. In addition, the mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably by weight. Ku is 1: 0.2 to 1: 5.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, pyraclonyl, carfentrazone ethyl, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is 1: It is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and fluropyroxifene benzyl and carfentrazone ethyl And the mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and The mixing ratio of fluropyroxifenebenzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0. To 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriftalide, carfentrazone ethyl, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriftalide is 1: It is in the range of 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and fluropyroxifene benzyl and carfentrazone ethyl And the mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 by weight. In the range of 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriminobacmethyl, carfentrazone ethyl, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriminobacmethyl is: The weight ratio is in the range of 1: 0.01 to 1:30, preferably 1: 0.05 to 1: 6, more preferably 1: 0.1 to 1: 3, and fluropyroxifenebenzyl. And carfentrazone ethyl are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. In addition, the mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably, by weight. It is 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, carfentrazone ethyl, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is a weight ratio. In the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and The mixing ratio with fentrazone ethyl is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. In addition, the mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably, by weight. It is 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, carfentrazone ethyl, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: The range of 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15, and The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The mixing ratio of piroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0 by weight. 2 to 1: 5.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, penoxsulam, carfentrazone ethyl, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and penoxsulam is 1: It is in the range of 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and fluropyraloxifene benzyl and carfentrazone ethyl. And the mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0. To 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, carfentrazone ethyl, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1: It is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and fluropyroxifenebenzyl and carfentrazone ethyl The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: .2～1: in the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, carfentrazone ethyl, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: It is in the range of 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and carfentrazone ethyl Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to : In the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, cumyluron, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is by weight, The range is from 1: 0.06 to 1: 150, preferably from 1: 0.3 to 1:30, and more preferably from 1: 0.6 to 1:15. The mixing ratio by weight is in the range of 1: 0.3 to 1: 800, preferably 1: 1.5 to 1: 160, more preferably 1: 3 to 1:80. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, cumyluron, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0.03 by weight. 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and the mixing ratio of fluropyroxifene benzyl and cumylron is: The weight ratio is in the range of 1: 0.3 to 1: 800, preferably 1: 1.5 to 1: 160, more preferably 1: 3 to 1:80, and fluropyroxifenebenzyl and imazosulfuron. Is a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromephone, cumyluron, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0.02 by weight ratio. 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and cumylron is a weight ratio. In the range of 1: 0.3 to 1: 800, preferably 1: 1.5 to 1: 160, more preferably 1: 3 to 1:80, and the addition of fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffeotrol, cumyluron, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is in a weight ratio of 1: 0.05 to The ratio of 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, and the mixing ratio of fluropyroxifene benzyl and cumylron is a weight ratio. In the range of 1: 0.3 to 1: 800, preferably 1: 1.5 to 1: 160, more preferably 1: 3 to 1:80, and the addition of fluropyroxifenebenzyl and imazosulfuron The mixing ratio is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, cumyluron, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0.02 by weight ratio. 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and cumylron is a weight ratio. In the range of 1: 0.3 to 1: 800, preferably 1: 1.5 to 1: 160, more preferably 1: 3 to 1:80, and the addition of fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, cumyluron, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is by weight, The range is from 1: 0.03 to 1:80, preferably from 1: 0.15 to 1:16, more preferably from 1: 0.3 to 1: 8, and between fluropyroxifenebenzyl and cumylron The mixing ratio by weight is in the range of 1: 0.3 to 1: 800, preferably 1: 1.5 to 1: 160, more preferably 1: 3 to 1:80. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyraclonyl, cumyluron, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyracuronil is from 1: 0.04 to The ratio of 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. In the range of 1: 0.3 to 1: 800, preferably 1: 1.5 to 1: 160, more preferably 1: 3 to 1:80, and The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriftalide, cumyluron, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriftalide is 1: 0.03 by weight ratio. The range is 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8. In the range of 1: 0.3 to 1: 800, preferably 1: 1.5 to 1: 160, more preferably 1: 3 to 1:80, and The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriminobacmethyl, cumyluron, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriminobacmethyl is in a weight ratio, The range is from 1: 0.01 to 1:30, preferably from 1: 0.05 to 1: 6, more preferably from 1: 0.1 to 1: 3. The mixing ratio by weight is in the range of 1: 0.3 to 1: 800, preferably 1: 1.5 to 1: 160, more preferably 1: 3 to 1:80. The mixing ratio of phenbenzyl and imazosulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, cumyluron, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is 1: The ratio is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. Is in the range of 1: 0.3 to 1: 800, preferably 1: 1.5 to 1: 160, more preferably 1: 3 to 1:80 by weight ratio. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, cumyluron, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and fentrazamide is 1: 0.1 by weight. 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15, and the mixing ratio of fluropyroxifene benzyl and cumylron is by weight, The range is from 1: 0.3 to 1: 800, preferably from 1: 1.5 to 1: 160, more preferably from 1: 3 to 1:80, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, penox slam, cumyluron, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and penox slam is 1: 0.01- by weight ratio. 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and the mixing ratio of fluropyroxifene benzyl and cumylron is expressed as a weight ratio. In the range of 1: 0.3 to 1: 800, preferably 1: 1.5 to 1: 160, more preferably 1: 3 to 1:80, and the addition of fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, cumyluron, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is in a weight ratio of 1: 0.04 to The ratio of 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. In the range of 1: 0.3 to 1: 800, preferably 1: 1.5 to 1: 160, more preferably 1: 3 to 1:80, and The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, cumyluron, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0.2 to The ratio is 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxyphenebenzyl and cumylron is 1: The range is from 0.3 to 1: 800, preferably from 1: 1.5 to 1: 160, more preferably from 1: 3 to 1:80, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is as follows: The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, chromeprop, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is a weight ratio, The range is from 1: 0.06 to 1: 150, preferably from 1: 0.3 to 1:30, more preferably from 1: 0.6 to 1:15. The mixing ratio by weight is in the range of 1: 0.1 to 1: 200, preferably 1: 0.5 to 1:40, more preferably 1: 1 to 1:20. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1. 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, chromeprop, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0.03 by weight. The range is 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and the mixing ratio of fluropyroxifene benzyl and chromeprop is The weight ratio is in the range of 1: 0.1 to 1: 200, preferably 1: 0.5 to 1:40, more preferably 1: 1 to 1:20, and fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromemephone, chromeprop, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0.02 by weight ratio. 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and chromep is And in the range of 1: 0.1 to 1: 200, preferably 1: 0.5 to 1:40, more preferably 1: 1 to 1:20, and the addition of fluropyroxifenebenzyl and imazosulfuron The mixing ratio is, by weight, 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, chromeprop, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is in a weight ratio of 1: 0.05 to The ratio of 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, and the mixing ratio of fluropyroxifene benzyl and chromeprop is a weight ratio. And in the range of 1: 0.1 to 1: 200, preferably 1: 0.5 to 1:40, more preferably 1: 1 to 1:20, and the addition of fluropyroxifenebenzyl and imazosulfuron The mixing ratio is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: by weight. It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, chromeprop, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0.02 by weight ratio. It is in the range of 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and chromep is the weight ratio. In the range of 1: 0.1 to 1: 200, preferably 1: 0.5 to 1:40, and more preferably 1: 1 to 1:20, and between fluoropyroxifenebenzyl and imazosulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, chromeprop, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is by weight, The range is from 1: 0.03 to 1:80, preferably from 1: 0.15 to 1:16, more preferably from 1: 0.3 to 1: 8. The mixing ratio by weight is in the range of 1: 0.1 to 1: 200, preferably 1: 0.5 to 1:40, more preferably 1: 1 to 1:20. The mixing ratio of phenbenzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: by weight. It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyraclonyl, chromeprop, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyracuronil is from 1: 0.04 to The ratio is 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. In the range of 1: 0.1 to 1: 200, preferably 1: 0.5 to 1:40, more preferably 1: 1 to 1:20, and The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriftalide, chromeprop, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriftalide is 1: 0.03 by weight. It is in the range of 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and the mixing ratio of fluropyroxifene benzyl and chromeprop is a weight ratio. In the range of 1: 0.1 to 1: 200, preferably 1: 0.5 to 1:40, and more preferably 1: 1 to 1:20, and between fluoropyroxifenebenzyl and imazosulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriminobacmethyl, chromeprop, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriminobacmethyl is a weight ratio, The range is from 1: 0.01 to 1:30, preferably from 1: 0.05 to 1: 6, more preferably from 1: 0.1 to 1: 3. The mixing ratio by weight is in the range of 1: 0.1 to 1: 200, preferably 1: 0.5 to 1:40, more preferably 1: 1 to 1:20. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, chromeprop, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is 1: It is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifenebenzyl and chromeprop Is in the range of 1: 0.1 to 1: 200, preferably 1: 0.5 to 1:40, more preferably 1: 1 to 1:20 by weight, and fluropyroxifenebenzyl. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, chromeprop, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0.1 by weight ratio. The ratio of 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15, and the mixing ratio of fluropyroxifene benzyl and chromeprop is by weight, It is in the range of 1: 0.1 to 1: 200, preferably 1: 0.5 to 1:40, more preferably 1: 1 to 1:20, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, penox slam, chromeprop, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and penox slam is 1: 0.01 to 1 by weight. The ratio of 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and the mixing ratio of fluropyroxifene benzyl and chromep is the weight ratio. And in the range of 1: 0.1 to 1: 200, preferably 1: 0.5 to 1:40, more preferably 1: 1 to 1:20, and the addition of fluropyroxifenebenzyl and imazosulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, chromeprop, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is from 1: 0.04 to The ratio is 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. In the range of 1: 0.1 to 1: 200, preferably 1: 0.5 to 1:40, more preferably 1: 1 to 1:20, and The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, chromeprop, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0.2 to The ratio is 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and chromeprop is 1: It is in the range of 0.1 to 1: 200, preferably 1: 0.5 to 1:40, more preferably 1: 1 to 1:20, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, cyclopyrimoleate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is weight Ratio of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and The mixing ratio with cyclopyrimoleate is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight. The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0, by weight. 2 to 1: 5.

When the composition of the present invention is a composition containing fluropyracoxifene benzyl, indanophan, cyclopyrimoleate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0 by weight. 0.03 to 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and fluropyroxifenebenzyl and cyclopyrimoleate. The mixing ratio by weight is from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15. The mixing ratio of piroxifenebenzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: by weight. It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromephone, cyclopyrimoleate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0 by weight. 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and there is also a difference between fluropyroxyphenebenzyl and cyclopyrimoleate. The mixing ratio by weight is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of phenbenzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1 by weight. 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, cyclopyrimolate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: 0 by weight. 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, and there is no difference between fluropyroxifenebenzyl and cyclopyrimoleate. The mixing ratio by weight is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of phenbenzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0. To 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, cyclopyrimolate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0 by weight. 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and The mixing ratio by weight is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, cyclopyrimolate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is: Ratio of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and The mixing ratio with cyclopyrimoleate is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight. The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0. To 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyracuronyl, cyclopyrimolate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is 1: 0 by weight. 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the addition of fluropyroxifenebenzyl and cyclopyrimoleate. The mixing ratio by weight is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriftalide, cyclopyrimolate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriftalide is 1: 0 by weight. 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and the addition of fluropyroxifenebenzyl and cyclopyrimoleate. The mixing ratio by weight is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of phenbenzyl and imazosulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriminobacmethyl, cyclopyrimoleate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriminobacmethyl is The ratio is in the range of 1: 0.01 to 1:30, preferably 1: 0.05 to 1: 6, more preferably 1: 0.1 to 1: 3. The mixing ratio with cyclopyrimoleate is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight. In addition, the mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 by weight. In the range of 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, cyclopyrimoleate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is expressed by weight ratio. 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, and more preferably 1: 0.4 to 1:10. The mixing ratio with morate is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight, The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 by weight. In the range of 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, cyclopyrimolate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0 by weight. The range is from 1: 1 to 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15, and the mixing ratio of fluropyroxifene benzyl and cyclopyrimoleate Is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight, and fluoropyroxifenebenzyl. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, penoxsulam, cyclopyrimolate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and penoxsulam is 1: 0 by weight. .01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and between fluoropyraoxifene benzyl and cyclopyrimoleate. The mixing ratio by weight is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, cyclopyrimolate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1: 0 by weight. 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the addition of fluropyroxifenebenzyl and cyclopyrimoleate. The mixing ratio by weight is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, cyclopyrimoleate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0 by weight. .2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxyphenebenzyl and cyclopyrimoleate is The weight ratio is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15, and fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, dimethatrine, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is a weight ratio, The range is from 1: 0.06 to 1: 150, preferably from 1: 0.3 to 1:30, more preferably from 1: 0.6 to 1:15. The mixing ratio by weight is in the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2. The mixing ratio of piroxifenebenzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: by weight. It is in the range of.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, dimethatrine, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0.03 by weight ratio. The ratio of 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and the mixing ratio of fluropyroxyphenebenzyl and dimethatrine is The weight ratio is in the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and fluropyroxifenebenzyl. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromephone, dimethatrine, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0.02 by weight ratio. 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and dimethatrine is a weight ratio. In the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and fluropyroxifenebenzyl and imazosulfuron. Is a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffeentrol, dimethatrine, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is in a weight ratio of 1: 0.05 to It is in the range of 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, and the mixing ratio of fluropyroxifene benzyl and dimethatrine is a weight ratio. In the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, dimethatrine, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0.02 by weight ratio. It is in the range of 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. In the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, dimethatrine, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is by weight, The range is from 1: 0.03 to 1:80, preferably from 1: 0.15 to 1:16, more preferably from 1: 0.3 to 1: 8. The mixing ratio by weight is in the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2. The mixing ratio of piroxifenebenzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight. It is in the range.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, pyracuronyl, dimethatrine, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyracuronil is 1: 0.04 to The ratio of 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxyphenebenzyl and dimethatrine is the weight ratio. In the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriftalide, dimethatrine, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriftalide is 1: 0.03 by weight ratio. The ratio of 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and the mixing ratio of fluropyroxyphenebenzyl and dimethatrine is a weight ratio. In the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriminobacmethyl, dimethatrine, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriminobacmethyl is a weight ratio, The range is from 1: 0.01 to 1:30, preferably from 1: 0.05 to 1: 6, more preferably from 1: 0.1 to 1: 3. The mixing ratio by weight is in the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2. The mixing ratio of piroxifenebenzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight. of It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, dimethatrine, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is 1: It is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifenebenzyl and dimethatrine Is in the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2 by weight. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, dimethatrine, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0.1 by weight ratio. 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15, and the mixing ratio of fluropyroxifene benzyl and dimethatrine is in a weight ratio, It is in the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and the addition of fluropyroxifene benzyl and imazosulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, penoxsulam, dimethatrine, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and penoxsulam is 1: 0.01 to 1 by weight. The ratio of 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and the mixing ratio of fluropyroxyphenebenzyl and dimethatrine is a weight ratio. In the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, dimethatrine, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is from 1: 0.04 to The ratio of 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxyphenebenzyl and dimethatrine is the weight ratio. In the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and fluropyroxifenebenzyl and imazosulfuron. Is a weight ratio in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, dimethatrine, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0.2 to The range is 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50. The mixing ratio of fluropyroxifenebenzyl and dimethatrine is 1: 5 by weight. It is in the range of 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight.

In the case where the composition of the present invention is a composition containing fluropyroxifenebenzyl, ipfencarbazone, dimrone, and imazosulfuron, the mixing ratio of fluropyroxifenebenzyl and ipfencarbazone is a weight ratio, The range is from 1: 0.06 to 1: 150, preferably from 1: 0.3 to 1:30, more preferably from 1: 0.6 to 1:15. The mixing ratio by weight is in the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, dimrone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0.03 by weight ratio. The range is 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and the mixing ratio of fluropyroxifene benzyl and dimulon is: The weight ratio is in the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25, and fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadiclomephone, dimuron, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0.02 by weight ratio. The ratio is 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. In the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25, and the addition of fluropyroxifenebenzyl and imazosulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, dimrone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is in a weight ratio of 1: 0.05 to The ratio is 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10. In the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25, and the addition of fluropyroxifenebenzyl and imazosulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, dimulone and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0.02 by weight ratio. The ratio is 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. In the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25, and the addition of fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, dimrone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is by weight, The range is from 1: 0.03 to 1:80, preferably from 1: 0.15 to 1:16, more preferably from 1: 0.3 to 1: 8. The mixing ratio by weight is in the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25. The mixing ratio of phenbenzyl and imazosulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyraclonyl, dimuron, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is from 1: 0.04 to The ratio is 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. In the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25, and The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriftalide, dimulone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriftalide is 1: 0.03 by weight ratio. The ratio is 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8. In the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25, and The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriminobacmethyl, dimrone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriminobacmethyl is in a weight ratio, The range is from 1: 0.01 to 1:30, preferably from 1: 0.05 to 1: 6, more preferably from 1: 0.1 to 1: 3. The mixing ratio by weight is in the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25. The mixing ratio of phenbenzyl and imazosulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. so That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, dimron, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is 1: The ratio is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. Is in the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25 by weight, and fluoropyroxifenebenzyl. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, dimuron, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0.1 by weight ratio. The ratio of 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15, and the mixing ratio of fluropyroxifene benzyl and dimulon is expressed as a weight ratio. It is in the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, penox slam, dimrone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and penox slam is 1: 0.01 to 1 by weight. The ratio is 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and the mixing ratio of fluropyroxifene benzyl and diimron is a weight ratio. In the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25, and the addition of fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, dimlon, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is in a weight ratio of 1: 0.04 to The ratio is 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. In the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25, and the addition of fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1: 5.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, dimrone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0.2 to The ratio is 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and diimron is 1: The range of 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifenebenzyl, ipfencarbazone, tefriltrione, and imazosulfuron, the mixing ratio of fluropyroxifenebenzyl and ipfencarbazone is a weight ratio. In the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15. The mixing ratio with furyltrione is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight, The mixing ratio of fluropyroxifene benzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2. In the range of 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, tefril trione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0. In the range of 03 to 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and The mixing ratio by weight is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is enclosed.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromephone, tefryltrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0. It is in the range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifenebenzyl and tefryltrione Is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight, and fluoropyroxifenebenzyl. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is in the range.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, tefryltrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: 0. The range is from 05 to 1: 100, preferably from 1: 0.25 to 1:20, more preferably from 1: 0.5 to 1:10. Is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to : In the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, tefryltrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0. It is in the range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifenebenzyl and tefryltrione Is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight, and fluropyroxifenebenzyl. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, tefryltrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is a weight ratio. In the range of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8. The mixing ratio with furyltrione ranges from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15 by weight, The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to weight ratio. : In the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyracuronyl, tefryltrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyracuronil is 1: 0. It is in the range of 04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifenebenzyl and tefryltrione Is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight, and fluoropyroxifenebenzyl. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriftalide, tefryltrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriftalide is 1: 0. It is in the range of 03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and the mixing ratio of fluropyroxifenebenzyl and tefryltrione Is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight, and fluoropyroxifenebenzyl. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriminobacmethyl, tefryltrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriminobacmethyl is a weight ratio. In the range of 1: 0.01 to 1:30, preferably 1: 0.05 to 1: 6, more preferably 1: 0.1 to 1: 3. The mixing ratio with furyltrione ranges from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15 by weight, The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1 by weight. 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, tefryltrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is by weight, It is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and fluropyroxifenebenzyl and tefryltrione The mixing ratio by weight is from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15. The mixing ratio of piroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1 by weight. 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, tefryltrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0. The ratio is from 1: 1 to 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15, and the mixing ratio of fluropyroxyphenebenzyl and tefryltrione is: The weight ratio is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15, and fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, penoxsulam, tefriltrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and penoxsulam is 1: 0. It is in the range of 01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and the mixing ratio of fluropyroxifenebenzyl and tefryltrione Is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight, and fluropyroxifenebenzyl. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, tefryltrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1: 0. It is in the range of 04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. Is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight, and fluropyroxifenebenzyl. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, tefril trione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0. 2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifenebenzyl and tefryltrione is expressed by weight ratio. In the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15, and the addition of fluropyroxifenebenzyl and imazosulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, pyrazoxifene, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is a weight ratio, It is in the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and it is also possible that fluoropyraloxifene benzyl and pyrazoxifene The mixing ratio by weight is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to : In the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, pyrazoxifene, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0.03 by weight ratio. The range is 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and the mixing ratio of fluropyroxyphenebenzyl and pyrazoxifene is: By weight ratio, it is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and it is also possible that fluoropyraloxifenebenzyl and imazosulfuron The mixing ratio is, by weight, 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromephone, pyrazoxifene, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0.02 by weight ratio. 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and pyrazoxifene is expressed as a weight ratio. In the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifenebenzyl and imazosulfuron Is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, pyrazoxifene, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is in a weight ratio of 1: 0.05 to It is in the range of 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, and the mixing ratio of fluropyroxifene benzyl and pyrazoxifene is in a weight ratio. In the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifenebenzyl and imazosulfuron Is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1. 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, pyrazoxifene, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0.02 by weight ratio. 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and pyrazoxifene is expressed as a weight ratio. In the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifenebenzyl and imazosulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, pyrazoxifene, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is by weight, The range is from 1: 0.03 to 1:80, preferably from 1: 0.15 to 1:16, more preferably from 1: 0.3 to 1: 8. The mixing ratio by weight is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1. 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyraclonyl, pyrazoxifene, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is 1: 0.04 to The ratio is 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxyphenebenzyl and pyrazoxifene is in a weight ratio. In the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifenebenzyl and imazosulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriftalide, pyrazoxifene, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriftalide is 1: 0.03 by weight ratio. It is in the range of 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and the mixing ratio of fluropyroxifene benzyl and pyrazoxifene is a weight ratio. In the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifenebenzyl and imazosulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight.

When the composition of the present invention is a composition containing fluropyracoxifene benzyl, pyriminobacmethyl, pyrazoxifene, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriminobacmethyl is a weight ratio, The range is from 1: 0.01 to 1:30, preferably from 1: 0.05 to 1: 6, more preferably from 1: 0.1 to 1: 3. The mixing ratio by weight is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50. And imazosulfuron are mixed at a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, pyrazoxifene, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is 1: It is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and pyrazoxifene Is in the range from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50, by weight ratio. Also, fluropyroxifene benzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, pyrazoxifene, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0.1 by weight ratio. 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15, and the mixing ratio of fluropyroxifene benzyl and pyrazoxifene is by weight, The range is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is as follows: In a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, penoxsulam, pyrazoxifene, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and penoxsulam is from 1: 0.01 to 1 by weight. The ratio of 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and the mixing ratio of fluropyroxifene benzyl and pyrazoxifene is a weight ratio. In the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifenebenzyl and imazosulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, pyrazoxifene, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is from 1: 0.04 to The ratio is 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxyphenebenzyl and pyrazoxifene is in a weight ratio. In the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifenebenzyl and imazosulfuron Is a weight ratio in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, pyrazoxifene and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0.2 to The ratio is 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50. The mixing ratio of fluropyroxifene benzyl and pyrazoxifene is 1: It is in the range of 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, pyrazolinate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is a weight ratio, The range is from 1: 0.06 to 1: 150, preferably from 1: 0.3 to 1:30, more preferably from 1: 0.6 to 1:15. The mixing ratio is in the range of 1: 0.6 to 1: 1500, preferably 1: 3 to 1: 300, more preferably 1: 6 to 1: 150, and fluropyroxifenebenzyl. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to : In the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, pyrazolinate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0.03 by weight ratio. It is in the range of 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and the mixing ratio of fluropyroxyphenebenzyl and pyrazolinate is: The weight ratio ranges from 1: 0.6 to 1: 1500, preferably from 1: 3 to 1: 300, and more preferably from 1: 6 to 1: 150. Further, the fluoropyraloxifene benzyl and imazosulfuron The mixing ratio is, by weight, 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromephone, pyrazolinate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0.02 in weight ratio. 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxyphenebenzyl and pyrazolinate is a weight ratio. In the range of 1: 0.6 to 1: 1500, preferably 1: 3 to 1: 300, more preferably 1: 6 to 1: 150, and the mixing ratio of fluropyroxifenebenzyl and imazosulfuron Is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is enclosed.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, caffeotrol, pyrazolinate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is in a weight ratio of 1: 0.05 to It is in the range of 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10. In the range of 1: 0.6 to 1: 1500, preferably 1: 3 to 1: 300, more preferably 1: 6 to 1: 150. Is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1. 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, pyrazolinate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0.02 by weight ratio. The ratio of 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. In the range of 1: 0.6 to 1: 1500, preferably 1: 3 to 1: 300, more preferably 1: 6 to 1: 150. Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. .

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, pyrazolinate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is by weight, The range is from 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8. The mixing ratio by weight is in the range of 1: 0.6 to 1: 1500, preferably 1: 3 to 1: 300, more preferably 1: 6 to 1: 150. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1. 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyracuronyl, pyrazolinate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyracuronil is 1: 0.04 to The ratio of 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. In the range of 1: 0.6 to 1: 1500, preferably 1: 3 to 1: 300, more preferably 1: 6 to 1: 150. Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriftalide, pyrazolinate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriftalide is 1: 0.03 by weight ratio. It is in the range of 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and the mixing ratio of fluropyroxifene benzyl and pyrazolinate is a weight ratio. In the range of 1: 0.6 to 1: 1500, preferably 1: 3 to 1: 300, more preferably 1: 6 to 1: 150, and the mixing ratio of fluropyroxifenebenzyl and imazosulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriminobacmethyl, pyrazolinate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriminobacmethyl is a weight ratio, It is in the range of 1: 0.01 to 1:30, preferably 1: 0.05 to 1: 6, more preferably 1: 0.1 to 1: 3, and it is also possible that fluoropyraloxifene benzyl and pyrazolinate The mixing ratio by weight is in the range of 1: 0.6 to 1: 1500, preferably 1: 3 to 1: 300, more preferably 1: 6 to 1: 150. And imazosulfuron are mixed at a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, pyrazolinate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is 1: It is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and pyrazolinate Is in the range of 1: 0.6 to 1: 1500, preferably 1: 3 to 1: 300, more preferably 1: 6 to 1: 150 by weight, and fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, pyrazolinate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0.1 by weight. 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15, and the mixing ratio of fluropyroxifene benzyl and pyrazolinate is by weight, The range is from 1: 0.6 to 1: 1500, preferably from 1: 3 to 1: 300, more preferably from 1: 6 to 1: 150, and the mixing ratio of fluropyroxifenebenzyl and imazosulfuron is as follows: In a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, penoxsulam, pyrazolinate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and penoxsulam is from 1: 0.01 to 1 by weight. The ratio of 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and the mixing ratio of fluropyroxyphenebenzyl and pyrazolinate is a weight ratio. In the range of 1: 0.6 to 1: 1500, preferably 1: 3 to 1: 300, more preferably 1: 6 to 1: 150, and the mixing ratio of fluropyroxifenebenzyl and imazosulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, pyrazolinate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is from 1: 0.04 to The ratio of 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxyphenebenzyl and pyrazolinate is a weight ratio. In the range of 1: 0.6 to 1: 1500, preferably 1: 3 to 1: 300, more preferably 1: 6 to 1: 150, and the mixing ratio of fluropyroxifenebenzyl and imazosulfuron Is a weight ratio in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, pyrazolinate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0.2 to The range is 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50. The mixing ratio of fluropyroxyphenebenzyl and pyrazolinate is 1: It is in the range of 0.6 to 1: 1500, preferably 1: 3 to 1: 300, more preferably 1: 6 to 1: 150, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron is a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifenebenzyl, ipfencarbazone, fenquinotrione, and imazosulfuron, the mixing ratio of fluropyroxifenebenzyl and ipfencarbazone is a weight ratio. In the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and fluoropyraoxifene benzyl and phen The mixing ratio with quinotrione ranges from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15 by weight, The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0, by weight. 2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, fenquinotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0. It is in the range of 03 to 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and it is also possible that fluropyroxyphenebenzyl and fenquinotrione The mixing ratio by weight is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of phenbenzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: by weight. It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadiclomephone, fenquinotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0. It is in the range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxyphenebenzyl and fenquinotrione Is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight, and fluoropyroxifenebenzyl. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1. 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, fenquinotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: 0. The range is from 05 to 1: 100, preferably from 1: 0.25 to 1:20, more preferably from 1: 0.5 to 1:10, and the mixing ratio of fluropyroxyphenebenzyl and fenquinotrione Is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight, and fluoropyroxifenebenzyl. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0. To 1: 5.

When the composition of the present invention is a composition containing fluropyroxyphenebenzyl, cyclopyranyl, phenquinotrione, and imazosulfuron, the mixing ratio of fluropyroxifenebenzyl and cyclopyranyl is 1: 0. It is in the range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxyphenebenzyl and fenquinotrione Is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight, and fluoropyroxifenebenzyl. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, fenquinotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is a weight ratio. In the range of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and fluoropyroxifenebenzyl and phen The mixing ratio with quinotrione ranges from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15 by weight, The mixing ratio of fluropyroxifenebenzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0. To 1: 5.

When the composition of the present invention is a composition containing fluropyroxyphenebenzyl, pyraclonyl, fenquinotrione, and imazosulfuron, the mixing ratio of fluropyroxifenebenzyl and pyraclonil is 1: 0. It is in the range of 04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxyphenebenzyl and fenquinotrione Is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight, and fluoropyroxifenebenzyl. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriftalide, phenquinotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriftalide is 1: 0. It is in the range of 03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and the mixing ratio of fluropyroxyphenebenzyl and fenquinotrione Is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight, and fluoropyroxifenebenzyl. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriminobacmethyl, phenquinotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriminobacmethyl is a weight ratio. In the range of 1: 0.01 to 1:30, preferably 1: 0.05 to 1: 6, more preferably 1: 0.1 to 1: 3, and fluoropyraoxifene benzyl and phen The mixing ratio with quinotrione ranges from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15 by weight, The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 by weight. In the range of 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, fenquinotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is in a weight ratio, It is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and fluropyroxyphenebenzyl and fenquinotrione The mixing ratio by weight is from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15. The mixing ratio of piroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 by weight. In the range of 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, fenquinotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0. The range is from 1: 1 to 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15, and the mixing ratio of fluropyroxyphenebenzyl and fenquinotrione is: The weight ratio is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15, and fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, penoxsulam, fenquinotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and penoxsulam is 1: 0. It is in the range of 01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and the mixing ratio of fluropyroxyphenebenzyl and fenquinotrione Is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight, and fluropyroxifenebenzyl. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, phenquinotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1: 0. It is in the range of 04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxyphenebenzyl and fenquinotrione Is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight, and fluropyroxifenebenzyl. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, fenquinotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0. It is in the range of 2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxyphenebenzyl and fenquinotrione is a weight ratio. In the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15, and the addition of fluropyroxifenebenzyl and imazosulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, benzobicyclone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is a weight ratio. In the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and fluoropyraoxifenebenzyl and benzo The mixing ratio with bicyclone is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10 by weight. The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: .2～1: in the range of 5.

When the composition of the present invention is a composition containing fluropyracoxifene benzyl, indanophan, benzobicyclone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0. The range is from 03 to 1:75, preferably from 1: 0.15 to 1:15, more preferably from 1: 0.3 to 1: 7.5. The mixing ratio by weight is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. The mixing ratio of piroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1 by weight. 5 is in the range of.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadiclomephone, benzobicyclone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and oxadiclomephone is 1: 0. The range is from 02 to 1:50, preferably from 1: 0.1 to 1:10, more preferably from 1: 0.2 to 1: 5. Is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and fluropyroxy by weight ratio. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to : In the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, benzobicyclone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: 0. The range is from 05 to 1: 100, preferably from 1: 0.25 to 1:20, more preferably from 1: 0.5 to 1:10. Is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and fluropyroxy by weight ratio. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0. 2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, benzobicyclone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0. The range is from 02 to 1:50, preferably from 1: 0.1 to 1:10, more preferably from 1: 0.2 to 1: 5. Is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and fluropyroxy by weight ratio. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, benzobicyclone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is a weight ratio. In the range of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and fluoropyraoxifenebenzyl and benzo The mixing ratio with bicyclone is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10 by weight. The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0, in weight ratio. 2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyraclonyl, benzobicyclone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is 1: 0. It is in the range of 04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifenebenzyl and benzobicyclon Is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10 by weight ratio. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriftalide, benzobicyclone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriftalide is 1: 0. It is in the range of 03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and the mixing ratio of fluropyroxifenebenzyl and benzobicyclon Is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10 by weight ratio. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriminobacmethyl, benzobicyclone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriminobacmethyl is a weight ratio. In the range of 1: 0.01 to 1:30, preferably 1: 0.05 to 1: 6, more preferably 1: 0.1 to 1: 3, and fluoropyraoxifenebenzyl and benzo The mixing ratio with bicyclone is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10 by weight. The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0. To 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, benzobicyclone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is by weight, The range is from 1: 0.04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10, and fluoropyraoxifenebenzyl and benzobicyclone. And the mixing ratio by weight is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0. To 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, benzobicyclone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0. The range is from 1: 1 to 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15, and the mixing ratio of fluropyroxyphenebenzyl and benzobicyclone is: The weight ratio is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and fluropyroxifenebenzyl. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, penoxsulam, benzobicyclon, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and penoxsulam is 1: 0. It is in the range of 01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and the mixing ratio of fluropyroxifenebenzyl and benzobicyclon Is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10 by weight ratio. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, benzobicyclone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1: 0. It is in the range of 04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifenebenzyl and benzobicyclon Is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10 by weight ratio. The mixing ratio of phenbenzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: by weight. It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, benzobicyclone, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0. 2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and benzobicyclon is a weight ratio. In the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, benzophenap, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is a weight ratio. In the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and fluoropyraoxifenebenzyl and benzo The mixing ratio with fenap ranges from 1: 0.2 to 1: 400, preferably from 1: 1 to 1:80, more preferably from 1: 2 to 1:40 by weight. The mixing ratio of piroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1 by weight. 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, benzophenap, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0. The range is from 03 to 1:75, preferably from 1: 0.15 to 1:15, more preferably from 1: 0.3 to 1: 7.5. The mixing ratio by weight is in the range of 1: 0.2 to 1: 400, preferably 1: 1 to 1:80, more preferably 1: 2 to 1:40. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromemephone, benzophenap, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0. It is in the range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and benzophenap Is in the range of 1: 0.2 to 1: 400, preferably 1: 1 to 1:80, more preferably 1: 2 to 1:40 by weight, and fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffeentrol, benzophenap, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: 0. The range is from 05 to 1: 100, preferably from 1: 0.25 to 1:20, more preferably from 1: 0.5 to 1:10, and the mixing ratio of fluropyroxifene benzyl and benzophenap Is in the range of 1: 0.2 to 1: 400, preferably 1: 1 to 1:80, more preferably 1: 2 to 1:40 by weight, and fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, benzophenap, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0. The range is from 02 to 1:50, preferably from 1: 0.1 to 1:10, more preferably from 1: 0.2 to 1: 5. Is in the range of 1: 0.2 to 1: 400, preferably 1: 1 to 1:80, more preferably 1: 2 to 1:40 by weight ratio. Is a weight ratio in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, benzophenap, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is a weight ratio. In the range of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and fluoropyraoxifenebenzyl and benzo The mixing ratio with fenap ranges from 1: 0.2 to 1: 400, preferably from 1: 1 to 1:80, more preferably from 1: 2 to 1:40 by weight. The mixing ratio of piroxifenebenzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: by weight. It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyraclonyl, benzophenap, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is 1: 0. It is in the range of 04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and benzophenap Is in the range of 1: 0.2 to 1: 400, preferably 1: 1 to 1:80, more preferably 1: 2 to 1:40 by weight, and fluropyroxifenebenzyl and imazosulfuron. Is a weight ratio in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriftalide, benzophenap, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriftalide is 1: 0. It is in the range of 03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and the mixing ratio of fluropyroxifene benzyl and benzophenap Is in the range of 1: 0.2 to 1: 400, preferably 1: 1 to 1:80, more preferably 1: 2 to 1:40 by weight, and fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriminobacmethyl, benzophenap, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriminobacmethyl is a weight ratio. In the range of 1: 0.01 to 1:30, preferably 1: 0.05 to 1: 6, more preferably 1: 0.1 to 1: 3, and fluoropyraoxifenebenzyl and benzo The mixing ratio with fenap ranges from 1: 0.2 to 1: 400, preferably from 1: 1 to 1:80, more preferably from 1: 2 to 1:40 by weight. The mixing ratio of piroxifene benzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, benzophenap, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is by weight, The range is from 1: 0.04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10, and fluropyroxifenebenzyl and benzophenap. The mixing ratio by weight is 1: 0.2 to 1: 400, preferably 1: 1 to 1:80, more preferably 1: 2 to 1:40. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, benzophenap, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0. The range is from 1: 1 to 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15, and the mixing ratio of fluropyroxifene benzyl and benzophenap is: The weight ratio ranges from 1: 0.2 to 1: 400, preferably from 1: 1 to 1:80, more preferably from 1: 2 to 1:40. The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, penoxsulam, benzophenap, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and penoxsulam is 1: 0. It is in the range of 01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and the mixing ratio of fluropyroxifene benzyl and benzophenap Is in the range of 1: 0.2 to 1: 400, preferably 1: 1 to 1:80, more preferably 1: 2 to 1:40 by weight, and fluropyroxifenebenzyl and imazosulfuron. Is a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, benzophenap and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1: 0. It is in the range of 04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and benzophenap Is in the range of 1: 0.2 to 1: 400, preferably 1: 1 to 1:80, more preferably 1: 2 to 1:40 by weight, and fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, benzophenap and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0. 2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and benzophenap is a weight ratio. In the range of 1: 0.2 to 1: 400, preferably 1: 1 to 1:80, more preferably 1: 2 to 1:40, and the mixing ratio of fluropyroxifenebenzyl and imazosulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, benfrate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is a weight ratio, The range is from 1: 0.06 to 1: 150, preferably from 1: 0.3 to 1:30, more preferably from 1: 0.6 to 1:15. The mixing ratio by weight is in the range of 1: 0.1 to 1: 300, preferably 1: 0.5 to 1:60, more preferably 1: 1 to 1:30. The mixing ratio of phenbenzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1 by weight. 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, benfrate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0.03 by weight. The range is 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and the mixing ratio of fluropyroxifene benzyl and benfrate is: By weight ratio, it is in the range of 1: 0.1 to 1: 300, preferably 1: 0.5 to 1:60, more preferably 1: 1 to 1:30, and fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromephone, benfresulfate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0.02 by weight ratio. It is in the range of 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The mixing ratio of fluropyroxifene benzyl and benfrate is the weight ratio. In the range of 1: 0.1 to 1: 300, preferably 1: 0.5 to 1:60, more preferably 1: 1 to 1:30, and the addition of fluropyroxifenebenzyl and imazosulfuron The mixing ratio is, by weight, 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffeentrol, benfrecetate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is in a weight ratio of 1: 0.05 to It is in the range of 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10. In the range of 1: 0.1 to 1: 300, preferably 1: 0.5 to 1:60, more preferably 1: 1 to 1:30, and The mixing ratio is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: by weight. It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, benfrate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0.02 by weight ratio. The ratio of 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and benfrate is the weight ratio. In the range of 1: 0.1 to 1: 300, preferably 1: 0.5 to 1:60, and more preferably 1: 1 to 1:30. Also, it is possible that fluoropyraloxifenebenzyl and imazosulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, benfrate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is by weight, The range is from 1: 0.03 to 1:80, preferably from 1: 0.15 to 1:16, more preferably from 1: 0.3 to 1: 8. The mixing ratio by weight is in the range of 1: 0.1 to 1: 300, preferably 1: 0.5 to 1:60, more preferably 1: 1 to 1:30. The mixing ratio of phenbenzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: by weight. It is in the range of.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, pyracuronyl, benfrate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is from 1: 0.04 to The ratio of 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and benfrate is the weight ratio. In the range of 1: 0.1 to 1: 300, preferably 1: 0.5 to 1:60, more preferably 1: 1 to 1:30, and the addition of fluropyroxifenebenzyl and imazosulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriftalide, benfrate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriftalide is 1: 0.03 by weight ratio. It is in the range of 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and the mixing ratio of fluropyroxifene benzyl and benfrate is the weight ratio. In the range of 1: 0.1 to 1: 300, preferably 1: 0.5 to 1:60, and more preferably 1: 1 to 1:30. Also, it is possible that fluoropyraloxifenebenzyl and imazosulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1: 5.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriminobacmethyl, benfrate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriminobacmethyl is by weight, It is in the range of 1: 0.01 to 1:30, preferably 1: 0.05 to 1: 6, more preferably 1: 0.1 to 1: 3. The mixing ratio by weight is in the range of 1: 0.1 to 1: 300, preferably 1: 0.5 to 1:60, more preferably 1: 1 to 1:30. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, benfrate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is 1: It is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and benfresate Is in the range of from 1: 0.1 to 1: 300, preferably from 1: 0.5 to 1:60, more preferably from 1: 1 to 1:30 by weight. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, benfrate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0.1 by weight ratio. The ratio of 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15, and the mixing ratio of fluropyroxifene benzyl and benfresate is expressed as a weight ratio. It is in the range of 1: 0.1 to 1: 300, preferably 1: 0.5 to 1:60, more preferably 1: 1 to 1:30, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, penoxsulam, benfrate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and penoxsulam is 1: 0.01- by weight ratio. The ratio of 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and the mixing ratio of fluropyroxifene benzyl and benfrate is the weight ratio. In the range of 1: 0.1 to 1: 300, preferably 1: 0.5 to 1:60, and more preferably 1: 1 to 1:30. Also, it is possible that fluoropyraloxifenebenzyl and imazosulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, benfrate, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is from 1: 0.04 to The ratio of 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and benfrate is the weight ratio. In the range of 1: 0.1 to 1: 300, preferably 1: 0.5 to 1:60, more preferably 1: 1 to 1:30, and the addition of fluropyroxifenebenzyl and imazosulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, benfrecetate and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0.2 to The range is 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and benfrecetate is 1: The range is from 0.1 to 1: 300, preferably from 1: 0.5 to 1:60, more preferably from 1: 1 to 1:30, and the mixing ratio of fluropyroxifenebenzyl and imazosulfuron is The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, mesotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is a weight ratio, The range is from 1: 0.06 to 1: 150, preferably from 1: 0.3 to 1:30, more preferably from 1: 0.6 to 1:15. The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The mixing ratio of piroxifenebenzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: by weight. It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, mesotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0.03 by weight ratio. The range is 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and the mixing ratio of fluropyroxifene benzyl and mesotrione is: The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromephone, mesotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0.02 by weight ratio. It is in the range of 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, mesotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: 0.05 to The ratio of 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, and the mixing ratio of fluropyroxyphenebenzyl and mesotrione is the weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, mesotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0.02 by weight ratio. 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and mesotrione is a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, mesotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is by weight, The range is from 1: 0.03 to 1:80, preferably from 1: 0.15 to 1:16, more preferably from 1: 0.3 to 1: 8. The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The mixing ratio of piroxifene benzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyracuronyl, mesotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is 1: 0.04 to It is in the range of 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxyphenebenzyl and mesotrione is a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriftalide, mesotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriftalide is 1: 0.03 by weight ratio. It is in the range of 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and the mixing ratio of fluropyroxyphenebenzyl and mesotrione is a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl and imazosulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriminobacmethyl, mesotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriminobacmethyl is a weight ratio, It is in the range of 1: 0.01 to 1:30, preferably 1: 0.05 to 1: 6, more preferably 1: 0.1 to 1: 3, and it is also possible that fluoropyraloxifenebenzyl and mesotrione The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The mixing ratio of piroxifenebenzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight. of It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, mesotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is 1: The ratio is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. The mixing ratio of phenbenzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, mesotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0.1 by weight ratio. 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15, and the mixing ratio of fluropyroxifene benzyl and mesotrione is, by weight, It is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and it is also possible that fluoropyruoxifenebenzyl and imazosulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, penoxsulam, mesotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and penoxsulam is 1: 0.01 to 1 by weight. The ratio of 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and the mixing ratio of fluropyroxifene benzyl and mesotrione is a weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, mesotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is from 1: 0.04 to The ratio is 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. Is a weight ratio in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, mesotrione, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0.2 to The ratio is 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxyphenebenzyl and mesotrione is 1: It is in the range of 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and imazosulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight.

When the composition of the present invention is a composition containing fluropyroxifenebenzyl, ipfencarbazone, lancotrione sodium salt, and imazosulfuron, the mixing ratio of fluropyroxifenebenzyl and ipfencarbazone is weight Ratio of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and The mixing ratio with the lancotrione sodium salt is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10 by weight. The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10 in terms of weight ratio. More preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, lancotrione sodium salt, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0 by weight. 0.03 to 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and fluropyroxifenebenzyl and lancotrione sodium salt And the mixing ratio by weight is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably by weight. It is properly 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadiclomephone, lancotrione sodium salt, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0 in weight ratio. 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the addition of fluropyroxifenebenzyl to lancotrione sodium salt. The mixing ratio by weight is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10. The mixing ratio of piroxifene benzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, The Mashiku 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffeotrol, lancotrione sodium salt, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: 0 by weight. 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, and the addition of fluropyroxifenebenzyl to lancotrione sodium salt The mixing ratio by weight is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10. The mixing ratio of piroxifene benzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, Preferably the al 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, lancotrione sodium salt, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0 by weight. 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the addition of fluropyroxifenebenzyl to lancotrione sodium salt. The mixing ratio by weight is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10. The mixing ratio of piroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably, by weight. 1: 0.2 to 1: 5.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, lancotrione sodium salt, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is: Ratio of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and The mixing ratio with the lancotrione sodium salt is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10 by weight. The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, by weight. Preferably the al 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyracuronyl, lancotrione sodium salt, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyracuronil is 1: 0 by weight. 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the addition of fluropyroxifenebenzyl to lancotrione sodium salt The mixing ratio by weight is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10. The mixing ratio of piroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably, by weight. 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriftalide, lancotrione sodium salt, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriftalide is 1: 0 by weight. 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and the addition of fluropyroxifenebenzyl to lancotrione sodium salt. The mixing ratio by weight is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10. The mixing ratio of piroxifene benzyl and imazosulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably : 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyriminobacmethyl, lancotrione sodium salt, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pyriminobacmethyl is weight The ratio is in the range of 1: 0.01 to 1:30, preferably 1: 0.05 to 1: 6, more preferably 1: 0.1 to 1: 3. The mixing ratio with the lancotrione sodium salt is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10 by weight. The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, by weight. Preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, lancotrione sodium salt, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is by weight. 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and fluropyroxifenebenzyl and lancotrione The mixing ratio with the sodium salt is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10 by weight. The mixing ratio of fluropyroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, by weight. Preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, lancotrione sodium salt, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0 by weight. 1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15, and the mixing ratio of fluropyroxifene benzyl and lancotrione sodium salt Is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10 by weight. The mixing ratio of phenbenzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably by weight. It is 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, penoxsulam, lancotrione sodium salt and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and penoxsulam is 1: 0 by weight. .01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and between fluropyroxifenebenzyl and lancotrione sodium salt. The mixing ratio by weight is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10. The mixing ratio of piroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably, by weight. 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, lancotrione sodium salt, and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1: 0 by weight. 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the addition of fluropyroxifenebenzyl to lancotrione sodium salt. The mixing ratio by weight is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10. The mixing ratio of piroxifene benzyl and imazosulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably by weight. Ku is 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, lancotrione sodium salt and imazosulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0 by weight. The range is from 2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50, and the mixing ratio of fluropyroxifenebenzyl and lancotrione sodium salt The weight ratio is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10. And imazosulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1. 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, carfentrazone ethyl, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone Is in the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and fluropyroxy by weight ratio. The mixing ratio of phenbenzyl and carfentrazone-ethyl is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1 by weight. The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, by weight. More Preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, carfentrazone ethyl, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is by weight, The range is from 1: 0.03 to 1:75, preferably from 1: 0.15 to 1:15, and more preferably from 1: 0.3 to 1: 7.5. The mixing ratio with fentrazone ethyl is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. In addition, the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably, by weight. 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadiclomephone, carfentrazone ethyl, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is in a weight ratio, It is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifene benzyl and carfentra The mixing ratio with zonethyl is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. In addition, the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably by weight. It is 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, carfentrazone ethyl, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is a weight ratio, It is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, and fluropyroxifene benzyl and carfentra The mixing ratio with zonethyl is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. The mixing ratio of fluropyroxifenebenzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10 by weight. The Mashiku 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, carfentrazone ethyl, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is in a weight ratio, It is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifene benzyl and carfentra The mixing ratio with zonethyl is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. The mixing ratio of fluropyroxifenebenzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: .2～1: in the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, carfentrazone ethyl, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet Is in the range of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8 by weight. The mixing ratio of phenbenzyl and carfentrazone-ethyl is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1 by weight. The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, by weight. further The Mashiku 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyracuronyl, carfentrazone ethyl, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is in a weight ratio, The range is from 1: 0.04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10, and fluropyroxifenebenzyl and carfentra The mixing ratio with zonethyl is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. The mixing ratio of fluropyroxifenebenzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: .2～1: in the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, carfentrazone ethyl, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is: The weight ratio is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and fluropyroxifenebenzyl. And carfentrazone ethyl are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably by weight. It is properly 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, carfentrazone ethyl, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is by weight, The range is from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15, and fluoropyraoxifene benzyl and carfentrazone ethyl The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1 by weight. 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, carfentrazone ethyl, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is by weight, The range is from 1: 0.04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10, and fluropyroxifenebenzyl and carfentra The mixing ratio with zonethyl is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably, by weight. : 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, carfentrazone ethyl, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is expressed by weight ratio, The range is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50. The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The mixing ratio of piroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0. To 1: 5.

When the composition of the present invention is a composition containing fluropyroxifenebenzyl, ipfencarbazone, cumyluron, and propyrisulfuron, the mixing ratio of fluropyroxifenebenzyl and ipfencarbazone is a weight ratio. In the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and fluropyroxifenebenzyl and cumylron The mixing ratio by weight is from 1: 0.3 to 1: 800, preferably from 1: 1.5 to 1: 160, more preferably from 1: 3 to 1:80. The mixing ratio of piroxifene benzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1. : It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, cumyluron, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0. It is in the range of 03 to 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and the mixing ratio of fluropyroxifene benzyl and cumylron Is in the range of 1: 0.3 to 1: 800, preferably 1: 1.5 to 1: 160, more preferably 1: 3 to 1:80 by weight ratio. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. so That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromephone, cumyluron, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0. The range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and cumylron is: The weight ratio ranges from 1: 0.3 to 1: 800, preferably from 1: 1.5 to 1: 160, and more preferably from 1: 3 to 1:80. The mixing ratio with pyrisulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, cumyluron, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: 0. The range is from 05 to 1: 100, preferably from 1: 0.25 to 1:20, more preferably from 1: 0.5 to 1:10. The weight ratio ranges from 1: 0.3 to 1: 800, preferably from 1: 1.5 to 1: 160, and more preferably from 1: 3 to 1:80. The mixing ratio with pyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, cumyluron, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0. 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and cumylron is: The weight ratio ranges from 1: 0.3 to 1: 800, preferably from 1: 1.5 to 1: 160, more preferably from 1: 3 to 1:80. The mixing ratio with pyrisulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, cumyluron, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is a weight ratio. In the range of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and fluropyroxifenebenzyl and cumyluron. The mixing ratio by weight is from 1: 0.3 to 1: 800, preferably from 1: 1.5 to 1: 160, more preferably from 1: 3 to 1:80. The mixing ratio of piroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1 by weight. : 5 It is in the range.

When the composition of the present invention is a composition containing fluropyroxifenebenzyl, pyraclonyl, cumyluron, and propyrisulfuron, the mixing ratio of fluropyroxifenebenzyl and pyracuronil is 1: 0. 04-1: 100, preferably 1: 0.2-1: 20, more preferably 1: 0.4-1: 10, and the mixing ratio of fluropyroxifenebenzyl and cumylron is The weight ratio ranges from 1: 0.3 to 1: 800, preferably from 1: 1.5 to 1: 160, and more preferably from 1: 3 to 1:80. The mixing ratio with pyrisulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, cumyluron, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is by weight, The range is from 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. The mixing ratio by weight is in the range of 1: 0.3 to 1: 800, preferably 1: 1.5 to 1: 160, more preferably 1: 3 to 1:80. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. of It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, cumyluron, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0. The ratio is from 1: 1 to 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15. In the range of 1: 0.3 to 1: 800, preferably 1: 1.5 to 1: 160, more preferably 1: 3 to 1:80, and fluropyroxifenebenzyl and propyrisulfuron. Is a weight ratio in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, cumyluron, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1: 0. 04-1: 100, preferably 1: 0.2-1: 20, more preferably 1: 0.4-1: 10, and the mixing ratio of fluropyroxifenebenzyl and cumylron is The weight ratio ranges from 1: 0.3 to 1: 800, preferably from 1: 1.5 to 1: 160, and more preferably from 1: 3 to 1:80. The mixing ratio with pyrisulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, cumyluron, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0. 2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and cumylron is expressed by weight. The range is from 1: 0.3 to 1: 800, preferably from 1: 1.5 to 1: 160, more preferably from 1: 3 to 1:80. The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, chromeprop, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is a weight ratio. In the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and fluropyroxifenebenzyl and chromeprop The mixing ratio by weight is from 1: 0.1 to 1: 200, preferably from 1: 0.5 to 1:40, more preferably from 1: 1 to 1:20. The mixing ratio of piroxifene benzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2. In the range of 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, chromeprop, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0. It is in the range of 03 to 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and the mixing ratio of fluropyroxifene benzyl and chromeprop Is in the range of 1: 0.1 to 1: 200, preferably 1: 0.5 to 1:40, more preferably 1: 1 to 1:20, by weight ratio. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is enclosed.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromemephone, chromeprop, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0. The range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The weight ratio ranges from 1: 0.1 to 1: 200, preferably from 1: 0.5 to 1:40, more preferably from 1: 1 to 1:20. The mixing ratio with pyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, chromeprop, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: 0. The range is from 05 to 1: 100, preferably from 1: 0.25 to 1:20, more preferably from 1: 0.5 to 1:10, and the mixing ratio of fluropyroxifene benzyl and chromeprop is The weight ratio is in the range of 1: 0.1 to 1: 200, preferably 1: 0.5 to 1:40, more preferably 1: 1 to 1:20, and fluropyroxifenebenzyl and pro The mixing ratio with pyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to : In the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, chromeprop, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0. The range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifenebenzyl and chromeprop is The weight ratio ranges from 1: 0.1 to 1: 200, preferably from 1: 0.5 to 1:40, more preferably from 1: 1 to 1:20. The mixing ratio with pyrisulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight. That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, chromeprop, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is a weight ratio. In the range of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and fluropyroxifenebenzyl and chromeprop The mixing ratio by weight is from 1: 0.1 to 1: 200, preferably from 1: 0.5 to 1:40, more preferably from 1: 1 to 1:20. The mixing ratio of piroxifenebenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to : In the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyraclonyl, chromeprop, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is 1: 0. The range is from 04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and chromeprop is The weight ratio is in the range of 1: 0.1 to 1: 200, preferably 1: 0.5 to 1:40, more preferably 1: 1 to 1:20, and fluropyroxifenebenzyl and pro The mixing ratio with pyrisulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, chromeprop, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is by weight, The range is from 1: 0.04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10. The mixing ratio by weight is in the range of 1: 0.1 to 1: 200, preferably 1: 0.5 to 1:40, more preferably 1: 1 to 1:20. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1. 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, chromeprop, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0. The range is from 1: 1 to 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15, and the mixing ratio of fluropyroxifene benzyl and chromeprop is a weight ratio. In the range of 1: 0.1 to 1: 200, preferably 1: 0.5 to 1:40, more preferably 1: 1 to 1:20, and fluropyroxifenebenzyl and propyrisulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, chromeprop, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1: 0. The range of 04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and chromeprop is The weight ratio ranges from 1: 0.1 to 1: 200, preferably from 1: 0.5 to 1:40, more preferably from 1: 1 to 1:20. The mixing ratio with pyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, chromeprop, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0. 2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and chromep is by weight, The range is from 1: 0.1 to 1: 200, preferably from 1: 0.5 to 1:40, more preferably from 1: 1 to 1:20, and it is also possible that fluoropyraloxifenebenzyl and propyrisulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, cyclopyrimolate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is In a weight ratio of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and fluropyroxifene The mixing ratio of benzyl and cyclopyrimoleate is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight. In addition, the mixing ratio of fluropyroxyphenebenzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1 in terms of weight ratio. 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, cyclopyrimoleate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1 by weight. : 0.03 to 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and fluropyroxifenebenzyl and cyclopyri The mixing ratio with morate is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight, The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 by weight. ~ : In the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromephone, cyclopyrimoleate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1 by weight. : 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl and cyclopyrimoleate The mixing ratio by weight is from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15. The mixing ratio of piroxifene benzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2. In the range of 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, cyclopyrimolate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1 by weight. : 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, and fluropyroxifenebenzyl and cyclopyrimoleate The mixing ratio by weight is from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15. The mixing ratio of piroxifene benzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: .2～1: in the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, cyclopyrimolate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1 by weight. : 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl and cyclopyrimoleate The mixing ratio by weight is from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15. The mixing ratio of piroxifene benzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1. : 5 It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, cyclopyrimoleate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is In a weight ratio of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and fluropyroxifene The mixing ratio of benzyl and cyclopyrimoleate is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight. In addition, the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1 in weight ratio. : .2～1: in the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyraclonyl, cyclopyrimolate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is 1 by weight. : 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and fluropyroxifenebenzyl and cyclopyrimoleate The mixing ratio by weight is from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15. The mixing ratio of piroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1 by weight. : 5 It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, cyclopyrimoleate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is: Ratio of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and The mixing ratio with cyclopyrimoleate is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight. In addition, the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0 by weight. 2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, cyclopyrimolate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1 by weight. : 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably in the range of 1: 1 to 1:15, and the addition of fluropyroxyphenebenzyl and cyclopyrimoleate The mixing ratio by weight is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, cyclopyrimoleate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1 by weight. : 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and fluropyroxifenebenzyl and cyclopyrimoleate The mixing ratio by weight is from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15. The mixing ratio of piroxifene benzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1. 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, cyclopyrimoleate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1 by weight. : 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxyphenebenzyl and cyclopyrimoleate Is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight, and fluropyroxifenebenzyl. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifenebenzyl, ipfencarbazone, dimethatrine, and propyrisulfuron, the mixing ratio of fluropyroxifenebenzyl and ipfencarbazone is a weight ratio. In the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and fluropyroxifenebenzyl and dimethatrine And the mixing ratio by weight is in the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2. The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 by weight. ~ : In the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, dimethatrine, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0. It is in the range of 03 to 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and the mixing ratio of fluropyroxifene benzyl and dimethatrine Is in the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2 by weight. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. Range of It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadiclomephone, dimethatrine, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and oxadiclomephone is 1: 0. The range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The weight ratio is in the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and fluropyroxifenebenzyl. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffeentrol, dimethatriline, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: 0. The range is from 05 to 1: 100, preferably from 1: 0.25 to 1:20, more preferably from 1: 0.5 to 1:10, and the mixing ratio of fluropyroxifene benzyl and dimethatrine is: The weight ratio is in the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and fluropyroxifenebenzyl. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1. 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, dimethatrine, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0. The range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The weight ratio is in the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and fluropyroxifenebenzyl. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. In .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, dimethatrine, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is a weight ratio. In the range of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and fluropyroxifenebenzyl and dimethatrine. And the mixing ratio by weight is in the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2. The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 by weight. ~ 1 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyraclonyl, dimethatrine, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is 1: 0. 04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and dimethatrine is: The weight ratio is in the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and fluropyroxifenebenzyl. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. In .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, dimethatrine, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is by weight, The range is from 1: 0.04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10. The mixing ratio by weight is in the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2. The mixing ratio of piroxifene benzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1. : It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, dimethatrine, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0. The ratio is from 1: 1 to 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15. In the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and fluropyroxifenebenzyl and pro The mixing ratio with pyrisulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight. That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, dimethatrine, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1: 0. 04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and dimethatrine is: The weight ratio is in the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and fluropyroxifenebenzyl. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, dimethatrine, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0. 2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and dimethatrine is expressed by weight ratio. It is in the range of 1: 0.01 to 1:20, preferably 1: 0.05 to 1: 4, more preferably 1: 0.1 to 1: 2, and fluropyroxifenebenzyl and propyrisulfuron The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, dimrone, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is a weight ratio. In the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and fluropyroxifenebenzyl and dimron The mixing ratio by weight is from 1: 0.1 to 1: 250, preferably from 1: 0.5 to 1:50, more preferably from 1: 1 to 1:25. The mixing ratio of piroxifene benzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1. : 5 It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, dimuron, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0. It is in the range of 03 to 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and the mixing ratio of fluropyroxifene benzyl and diimron Is in the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25 by weight, and fluoropyroxifenebenzyl. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. In .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadiclomephone, dimuron, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0. The range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and dimulon is The weight ratio is in the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25. In addition, fluropyroxifene benzyl and pro The mixing ratio with pyrisulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight. That.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, dimrone, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: 0. The range is from 05 to 1: 100, preferably from 1: 0.25 to 1:20, more preferably from 1: 0.5 to 1:10, and the mixing ratio of fluropyroxifene benzyl and diimron is: The weight ratio is in the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25, and fluropyroxifene benzyl and pro The mixing ratio with pyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, diimron, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0. The range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and dimulon is The weight ratio is in the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25, and fluropyroxifene benzyl and pro The mixing ratio with pyrisulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight. .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, dimlon, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is a weight ratio. In the range of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and fluropyroxifenebenzyl and dimron The mixing ratio by weight is 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25. The mixing ratio of piroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1 by weight. : 5 It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyraclonyl, diimron, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is 1: 0. It is in the range of 04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. The weight ratio ranges from 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25. The mixing ratio with pyrisulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, dimrone, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is by weight, The range is from 1: 0.04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10. The mixing ratio by weight is in the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. Range of It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, diimron, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0. The range is from 1: 1 to 150, preferably from 1: 0.5 to 1:30, and more preferably from 1: 1 to 1:15. In the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25, and fluropyroxifenebenzyl and propyrisulfuron The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, dimlon, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1: 0. It is in the range of 04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and dimulon is The weight ratio is in the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25. In addition, fluropyroxifene benzyl and pro The mixing ratio with pyrisulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, dimrone, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0. 2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and dimulon is expressed as a weight ratio. It is in the range of 1: 0.1 to 1: 250, preferably 1: 0.5 to 1:50, more preferably 1: 1 to 1:25, and it is also possible that fluoropyraloxifene benzyl and propyrisulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifenebenzyl, ipfencarbazone, tefriltrione, and propyrisulfuron, the mixing ratio of fluropyroxifenebenzyl and ipfencarbazone is: The weight ratio is in the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and fluropyroxifenebenzyl. And tefryltrione are mixed in a weight ratio of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. In addition, the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0 by weight. 2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, tefryltrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: It is in the range of 0.03 to 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and fluropyroxifenebenzyl and tefryltrione The mixing ratio by weight is from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15. The mixing ratio of piroxifene benzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1. : It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromephone, tefryltrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: It is in the range of 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and it is also possible that fluoropyraloxifenebenzyl and tefryltrione The mixing ratio by weight is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1. 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, tefryltrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: It is in the range of 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, and it is also possible that fluoropyraloxifenebenzyl and tefryltrione The mixing ratio by weight is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of phenbenzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0. To 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, tefryltrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: The range of 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and The mixing ratio by weight is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. Range of It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, tefryltrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is: The weight ratio is in the range of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and fluropyroxifene benzyl. And tefryltrione are mixed in a weight ratio of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. In addition, the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0 by weight. . To 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyraclonyl, tefryltrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is 1: It is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the addition of fluropyroxifenebenzyl and tefryltrione. The mixing ratio by weight is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. Range of It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, tefryltrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is a weight ratio. In the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. The mixing ratio with furyltrione ranges from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15 by weight, The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 by weight. In the range of 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, tefryltrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: The range is from 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15. Is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight, and fluropyroxifenebenzyl. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, tefryltrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1: It is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the addition of fluropyroxifenebenzyl and tefryltrione. The mixing ratio by weight is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, tefryltrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: The range is from 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50. The weight ratio is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. In addition, fluropyroxifenebenzyl and pro The mixing ratio with pyrisulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight. That.

When the composition of the present invention is a composition containing fluropyroxifenebenzyl, ipfencarbazone, pyrazoxifene, and propyrisulfuron, the mixing ratio of fluropyroxifenebenzyl and ipfencarbazone is a weight ratio. In the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15. The mixing ratio by weight is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50. The mixing ratio of phenbenzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0. To 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, pyrazoxifene, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0. It is in the range of 03 to 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and the mixing ratio of fluropyroxifene benzyl and pyrazoxifene Is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50 by weight, and fluropyroxifene benzyl and pro The mixing ratio with pyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadiclomephone, pyrazoxifene, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0. The range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The weight ratio ranges from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, pyrazoxifene, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: 0. The range is from 05 to 1: 100, preferably from 1: 0.25 to 1:20, more preferably from 1: 0.5 to 1:10, and the mixing ratio of fluropyroxifene benzyl and pyrazoxifene is: The weight ratio ranges from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50. Also, fluorpyroxifenebenzyl and propyrisulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2. In the range of 1: 5.

When the composition of the present invention is a composition containing fluropyroxifenebenzyl, cyclopyranyl, pyrazoxifene, and propyrisulfuron, the mixing ratio of fluropyroxifenebenzyl and cyclopyranyl is 1: 0. The range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The weight ratio ranges from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, pyrazoxifene, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is a weight ratio. In the range of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and fluropyroxifenebenzyl and pyrazoxifene The mixing ratio by weight is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2. In the range of 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyraclonyl, pyrazoxifene, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is 1: 0. The range is from 04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10. The weight ratio ranges from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, pyrazoxifene, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is by weight, The range is from 1: 0.04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10. The mixing ratio by weight is in the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to : In the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, pyrazoxifene, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0. The ratio is from 1: 1 to 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15, and the mixing ratio of fluropyroxifene benzyl and pyrazoxifene is in a weight ratio. In the range of 1: 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and fluropyroxifenebenzyl and propyrisulfuron The mixing ratio is, by weight, 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, pyrazoxifene, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1: 0. The range is from 04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and pyrazoxifene is: The weight ratio ranges from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50. Also, fluorpyroxifenebenzyl and propyrisulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, pyrazoxifene, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0. 2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxyphenebenzyl and pyrazoxifene is by weight, The range is from 1: 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50, and the mixing ratio of fluropyroxyphenebenzyl and propyrisulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. .

When the composition of the present invention is a composition containing fluropyroxifenebenzyl, ipfencarbazone, pyrazolinate, and propyrisulfuron, the mixing ratio of fluropyroxifenebenzyl and ipfencarbazone is a weight ratio. In the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and fluoropyroxifenebenzyl and pyrazolinate The mixing ratio by weight is in the range of 1: 0.6 to 1: 1500, preferably 1: 3 to 1: 300, more preferably 1: 6 to 1: 150. The mixing ratio of phenbenzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0. To 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, pyrazolinate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0. It is in the range of 03 to 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and the mixing ratio of fluropyroxifene benzyl and pyrazolinate Is in the range of 1: 0.6 to 1: 1500, preferably 1: 3 to 1: 300, more preferably 1: 6 to 1: 150 by weight, and fluropyroxifenebenzyl and pro The mixing ratio with pyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromephone, pyrazolinate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0. The range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and pyrazolinate is The weight ratio ranges from 1: 0.6 to 1: 1500, preferably from 1: 3 to 1: 300, more preferably from 1: 6 to 1: 150, and fluropyroxifenebenzyl and propyrisulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: It is in the range of.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, caffeotrol, pyrazolinate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: 0. The range is from 05 to 1: 100, preferably from 1: 0.25 to 1:20, more preferably from 1: 0.5 to 1:10, and the mixing ratio of fluropyroxifene benzyl and pyrazolinate is: The weight ratio ranges from 1: 0.6 to 1: 1500, preferably from 1: 3 to 1: 300, more preferably from 1: 6 to 1: 150, and fluropyroxifenebenzyl and propyrisulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2. In the range of 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, pyrazolinate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0. The range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and pyrazolinate is The weight ratio ranges from 1: 0.6 to 1: 1500, preferably from 1: 3 to 1: 300, more preferably from 1: 6 to 1: 150, and fluropyroxifenebenzyl and propyrisulfuron. Is a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, pyrazolinate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is a weight ratio. In the range of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and fluoropyroxifenebenzyl and pyrazolinate The mixing ratio by weight is 1: 0.6 to 1: 1500, preferably 1: 3 to 1: 300, more preferably 1: 6 to 1: 150. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2. In the range of 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyraclonyl, pyrazolinate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is 1: 0. The range of 04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and pyrazolinate is The weight ratio ranges from 1: 0.6 to 1: 1500, preferably from 1: 3 to 1: 300, more preferably from 1: 6 to 1: 150, and fluropyroxifenebenzyl and propyrisulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, pyrazolinate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is in a weight ratio, The range is from 1: 0.04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10, and between fluoropyraoxifenebenzyl and pyrazolinate The mixing ratio is in the range of 1: 0.6 to 1: 1500, preferably 1: 3 to 1: 300, more preferably 1: 6 to 1: 150, and fluropyroxifenebenzyl. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to : In the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, pyrazolinate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0. The ratio is from 1: 1 to 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15. In the range of 1: 0.6 to 1: 1500, preferably 1: 3 to 1: 300, more preferably 1: 6 to 1: 150, and The mixing ratio is, by weight, 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, pyrazolinate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1: 0. The range is from 04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and pyrazolinate is: The weight ratio ranges from 1: 0.6 to 1: 1500, preferably from 1: 3 to 1: 300, more preferably from 1: 6 to 1: 150, and fluropyroxifenebenzyl and propyrisulfuron. The mixing ratio is 1 to 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1: 5. It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, pyrazolinate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0. 2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and pyrazolinate is by weight, It is in the range of 1: 0.6 to 1: 1500, preferably 1: 3 to 1: 300, more preferably 1: 6 to 1: 150, and the mixing ratio of fluropyroxifenebenzyl and propyrisulfuron Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, fenquinotrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is: The weight ratio is in the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and fluropyroxifenebenzyl. And fenquinotrione are mixed in a weight ratio of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1 by weight. 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, fenquinotrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: It is in the range of 0.03 to 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and fluropyroxyphenebenzyl and fenquinotrione The mixing ratio by weight is from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15. The mixing ratio of piroxifenebenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to : In the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromephone, fenquinotrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: The range is 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The mixing ratio by weight is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2. In the range of 1: 5.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, fenquinotrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: The range is from 0.05 to 1: 100, preferably from 1: 0.25 to 1:20, more preferably from 1: 0.5 to 1:10. The mixing ratio by weight is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: .2～1: in the range of 5.

When the composition of the present invention is a composition containing fluropyroxyphenebenzyl, cyclopyranyl, fenquinotrione, and propyrisulfuron, the mixing ratio of fluropyroxyphenebenzyl and cyclopyranyl is 1: It is in the range of 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and it is also possible that fluoropyruoxiphenebenzyl and fenquinotrione The mixing ratio by weight is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, fenquinotrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is: The weight ratio is in the range of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and fluropyroxifene benzyl. And fenquinotrione are mixed in a weight ratio of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of fluropyroxifenebenzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: .2～1: in the range of 5.

When the composition of the present invention is a composition containing fluropyroxyphenebenzyl, pyraclonyl, phenquinotrione, and propyrisulfuron, the mixing ratio of fluropyroxyphenebenzyl and pyraclonil is 1: It is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and there is also a difference between fluropyroxyphenebenzyl and fenquinotrione. The mixing ratio by weight is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, phenquinotrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is a weight ratio. In the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and fluoropyraoxifene benzyl and phen The mixing ratio with quinotrione ranges from 1: 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15 by weight, The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0 by weight. 2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, fenquinotrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: It is in the range of 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. Is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15 by weight, and fluropyroxifenebenzyl. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, fenquinotrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1: It is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and it is also possible that fluoropyruoxifenebenzyl and fenquinotrione The mixing ratio by weight is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1. 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, fenquinotrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: The range is from 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50. The weight ratio is in the range of 1: 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably 1: 1 to 1:15. In addition, fluropyroxifenebenzyl and pro The mixing ratio with pyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifenebenzyl, ipfencarbazone, benzobicyclone, and propyrisulfuron, the mixing ratio of fluropyroxifenebenzyl and ipfencarbazone is: The weight ratio is in the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and fluropyroxifenebenzyl. And benzobicyclone are mixed in a weight ratio of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably, by weight. : 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, benzobicyclone, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: It is in the range of 0.03 to 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and fluropyroxifenebenzyl and benzobicyclone And the mixing ratio by weight is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2, by weight. In the range of 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadiclomephone, benzobicyclone, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and oxadiclomephone is 1: The range of 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and The mixing ratio by weight is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. The mixing ratio of piroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0. To 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, benzobicyclone, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: The range is from 0.05 to 1: 100, preferably from 1: 0.25 to 1:20, more preferably from 1: 0.5 to 1:10. The mixing ratio by weight is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. The mixing ratio of piroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1 by weight. 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, benzobicyclone, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: It is in the range of 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and it is also possible that fluoropyraloxifenebenzyl and benzobicyclon The mixing ratio by weight is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. The mixing ratio of piroxifene benzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1. : It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, benzobicyclone, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is: The weight ratio is in the range of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and fluropyroxifene benzyl. And benzobicyclone are mixed in a weight ratio of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. In addition, the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1 in weight ratio. 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyraclonyl, benzobicyclone, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is 1: It is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and it is also possible that fluoropyraloxifenebenzyl and benzobicyclon The mixing ratio by weight is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. The mixing ratio of piroxifene benzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1. : It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, benzobicyclone, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is a weight ratio. In the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and fluoropyraoxifenebenzyl and benzo The mixing ratio with bicyclone is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10 by weight. The mixing ratio of fluropyroxifenebenzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: .2～1: in the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, benzobicyclone, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: The range is from 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15, and the mixing ratio of fluropyroxyphenebenzyl and benzobicyclon Is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and fluropyroxy by weight ratio. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1. 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, benzobicyclone, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1: It is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, and more preferably 1: 0.4 to 1:10. The mixing ratio by weight is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. The mixing ratio of piroxifenebenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to : In the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, benzobicyclone, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: The range is from 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50, and the mixing ratio of fluropyroxyphenebenzyl and benzobicyclone is: The weight ratio is in the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and fluropyroxifenebenzyl. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, benzophenap, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is: The weight ratio is in the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and fluropyroxifenebenzyl. The mixing ratio of benzophenap and benzophenap ranges from 1: 0.2 to 1: 400, preferably from 1: 1 to 1:80, more preferably from 1: 2 to 1:40, by weight, The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 by weight. In the range of 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, benzophenap, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: It is in the range of 0.03 to 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and fluropyroxifene benzyl and benzophenap The mixing ratio by weight is in the range of 1: 0.2 to 1: 400, preferably 1: 1 to 1:80, more preferably 1: 2 to 1:40. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. of It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadiclomephone, benzophenap, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and oxadiclomephone is 1: It is in the range of 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and The mixing ratio by weight is in the range of 1: 0.2 to 1: 400, preferably 1: 1 to 1:80, more preferably 1: 2 to 1:40. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffeentrol, benzophenap, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: The range of 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, and The mixing ratio is in the range of 1: 0.2 to 1: 400, preferably 1: 1 to 1:80, more preferably 1: 2 to 1:40, and fluropyroxifenebenzyl. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to : In the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, benzophenap, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: It is in the range of 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and it can be used between fluropyroxifene benzyl and benzophenap. The mixing ratio by weight is in the range of 1: 0.2 to 1: 400, preferably 1: 1 to 1:80, more preferably 1: 2 to 1:40. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. so That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, benzophenap, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is: The weight ratio is in the range of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and fluropyroxifene benzyl. The mixing ratio of benzophenap and benzophenap ranges from 1: 0.2 to 1: 400, preferably from 1: 1 to 1:80, more preferably from 1: 2 to 1:40 by weight, The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2, by weight. ~ : In the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyraclonyl, benzophenap, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is 1: It is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and it can be used between fluropyroxifenebenzyl and benzophenap. The mixing ratio is in the range of 1: 0.2 to 1: 400, preferably 1: 1 to 1:80, more preferably 1: 2 to 1:40, and fluropyroxifenebenzyl. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. so That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, benzophenap, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is a weight ratio. In the range of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and fluoropyraoxifenebenzyl and benzo The mixing ratio with fenap ranges from 1: 0.2 to 1: 400, preferably from 1: 1 to 1:80, more preferably from 1: 2 to 1:40 by weight. The mixing ratio of piroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1 by weight. 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifenebenzyl, fentolazamide, benzophenap, and propyrisulfuron, the mixing ratio of fluropyroxifenebenzyl and fentolazamide is 1: The range is from 0.1 to 1: 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15. Is in the range of 1: 0.2 to 1: 400, preferably 1: 1 to 1:80, more preferably 1: 2 to 1:40 by weight, and fluropyroxifene benzyl and pro The mixing ratio with pyrisulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, benzophenap, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1: It is in the range of 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and it is also possible that fluoropyraloxifene benzyl and benzophenap The mixing ratio by weight is in the range of 1: 0.2 to 1: 400, preferably 1: 1 to 1:80, more preferably 1: 2 to 1:40. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, benzophenap, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: The range is from 0.2 to 1: 500, preferably from 1: 1 to 1: 100, more preferably from 1: 2 to 1:50. The weight ratio ranges from 1: 0.2 to 1: 400, preferably from 1: 1 to 1:80, more preferably from 1: 2 to 1:40. Is a weight ratio in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, benfrate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is a weight ratio. In the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and fluorpyroxifenebenzyl and benfrate The mixing ratio by weight is from 1: 0.1 to 1: 300, preferably from 1: 0.5 to 1:60, more preferably from 1: 1 to 1:30. The mixing ratio of piroxifene benzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2. In the range of 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, benfrate and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0. The range is from 03 to 1:75, preferably from 1: 0.15 to 1:15, more preferably from 1: 0.3 to 1: 7.5. Is in the range of from 1: 0.1 to 1: 300, preferably from 1: 0.5 to 1:60, more preferably from 1: 1 to 1:30 by weight. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is enclosed.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromephone, benfresulfate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1: 0. The range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifene benzyl and benfrate is: The weight ratio is in the range of 1: 0.1 to 1: 300, preferably 1: 0.5 to 1:60, more preferably 1: 1 to 1:30. The mixing ratio with pyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. It is in the range.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, benfresulfate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: 0. The range is from 05 to 1: 100, preferably from 1: 0.25 to 1:20, more preferably from 1: 0.5 to 1:10. The weight ratio is in the range of 1: 0.1 to 1: 300, preferably 1: 0.5 to 1:60, more preferably 1: 1 to 1:30. The mixing ratio with pyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to : In the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, benfrate and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0. The range of 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The weight ratio is in the range of 1: 0.1 to 1: 300, preferably 1: 0.5 to 1:60, more preferably 1: 1 to 1:30, and fluropyroxifene benzyl and pro The mixing ratio with pyrisulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight. That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, benfrate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is a weight ratio. In the range of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and fluorpyroxifenebenzyl and benfrate The mixing ratio by weight is from 1: 0.1 to 1: 300, preferably from 1: 0.5 to 1:60, more preferably from 1: 1 to 1:30. The mixing ratio of piroxifene benzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to : In the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyraclonyl, benfrate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is 1: 0. The range is from 04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10. The weight ratio is in the range of 1: 0.1 to 1: 300, preferably 1: 0.5 to 1:60, more preferably 1: 1 to 1:30. Further, fluropyroxifene benzyl and pro The mixing ratio with pyrisulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight. That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, benfresulfate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is in a weight ratio, The range is from 1: 0.04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10. The mixing ratio by weight is in the range of 1: 0.1 to 1: 300, preferably 1: 0.5 to 1:60, more preferably 1: 1 to 1:30. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1. 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, benfrate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0. The range is from 1: 1 to 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15, and the mixing ratio of fluropyroxifene benzyl and benfrate is the weight ratio. In the range of 1: 0.1 to 1: 300, preferably 1: 0.5 to 1:60, more preferably 1: 1 to 1:30, and fluropyroxifenebenzyl and propyrisulfuron. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, benfrate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1: 0. The range of 04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifene benzyl and benfrate is: The weight ratio is in the range of 1: 0.1 to 1: 300, preferably 1: 0.5 to 1:60, more preferably 1: 1 to 1:30. Further, fluropyroxifene benzyl and pro The mixing ratio with pyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, benfrate, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0. 2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and benfrate is in a weight ratio, The range is from 1: 0.1 to 1: 300, preferably from 1: 0.5 to 1:60, more preferably from 1: 1 to 1:30, and it is also possible that fluoropyraloxifenebenzyl and propyrisulfuron The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, mesotrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is a weight ratio. In the range of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and fluoropyroxifenebenzyl and mesotrione The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 by weight. ~ : In the range of 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, mesotrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1: 0. It is in the range of 03 to 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and the mixing ratio of fluropyroxifenebenzyl and mesotrione Is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5 by weight. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. Range of It is.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadiclomephone, mesotrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and oxadiclomephone is 1: 0. 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifenebenzyl and mesotrione is: The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. It is enclosed.

In the case where the composition of the present invention is a composition containing fluropyroxifene benzyl, caffeotrol, mesotrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1: 0. The range is from 05 to 1: 100, preferably from 1: 0.25 to 1:20, more preferably from 1: 0.5 to 1:10, and the mixing ratio of fluropyroxifene benzyl and mesotrione is: The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1. 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, mesotrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1: 0. 02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and the mixing ratio of fluropyroxifenebenzyl and mesotrione is: The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. In .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, mesotrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is a weight ratio. In the range of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and fluoropyroxifenebenzyl and mesotrione The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 by weight. ~ 1 5 is in the range of.

When the composition of the present invention is a composition containing fluropyroxifenebenzyl, pyraclonyl, mesotrione, and propyrisulfuron, the mixing ratio of fluropyroxifenebenzyl and pyraclonil is 1: 0. The range is from 04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10, and the mixing ratio of fluropyroxifenebenzyl and mesotrione is: The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. In .

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, mesotrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is by weight, The range is from 1: 0.04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10, and between fluoropyroxifenebenzyl and mesotrione. The mixing ratio by weight is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The mixing ratio of piroxifene benzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, and more preferably 1: 0.2 to 1. : It is in the range of.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, mesotrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1: 0. The range is from 1: 1 to 150, preferably from 1: 0.5 to 1:30, more preferably from 1: 1 to 1:15, and the mixing ratio of fluropyroxyphenebenzyl and mesotrione is expressed by weight ratio. In the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluoropyraoxifenebenzyl and pro The mixing ratio with pyrisulfuron is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, by weight. That.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, mesotrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1: 0. The range is from 04 to 1: 100, preferably from 1: 0.2 to 1:20, more preferably from 1: 0.4 to 1:10. The weight ratio is in the range of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. And propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. A.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, mesotrione, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1: 0. 2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifene benzyl and mesotrione is, by weight, 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5. The mixing ratio by weight is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, ipfencarbazone, lancotrione sodium salt, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and ipfencarbazone is , In a weight ratio of 1: 0.06 to 1: 150, preferably 1: 0.3 to 1:30, more preferably 1: 0.6 to 1:15, and fluropyroxifene The mixing ratio of benzyl and lancotrione sodium salt is 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10 by weight. In addition, the mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1: 1, by weight. 0, more preferably from 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, indanophan, lancotrione sodium salt, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and indanophan is 1 by weight. : 0.03 to 1:75, preferably 1: 0.15 to 1:15, more preferably 1: 0.3 to 1: 7.5, and fluropyroxifenebenzyl and lancotrione The mixing ratio with the sodium salt is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10 by weight. The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10 by weight. Preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, oxadichromemephone, lancotrione sodium salt, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and oxadichromephone is 1 by weight. : 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl and lancotrione sodium salt And the mixing ratio by weight is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, and The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, by weight. Preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, caffentrol, lancotrione sodium salt, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and caffentrol is 1 by weight. : 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, and fluropyroxifenebenzyl and lancotrione sodium salt And the mixing ratio by weight is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, and , Fluoropiroxifene benzyl and propyrisulfuron are mixed in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1: 1. , More preferably from 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, cyclopyranyl, lancotrione sodium salt, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and cyclopyranyl is 1 by weight. : 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5, and fluropyroxifenebenzyl and lancotrione sodium salt And the mixing ratio by weight is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably by weight. Ku is 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, tetoflupyrrolemet, lancotrione sodium salt, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and tetoflupyrrolemet is In a weight ratio of 1: 0.03 to 1:80, preferably 1: 0.15 to 1:16, more preferably 1: 0.3 to 1: 8, and fluropyroxifene The mixing ratio of benzyl and lancotrione sodium salt is 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10 by weight. The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1: 1 by weight. , More preferably from 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pyraclonyl, lancotrione sodium salt, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pyraclonil is 1 by weight. : 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and fluropyroxifenebenzyl and lancotrione sodium salt And the mixing ratio by weight is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably by weight. Ku is 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, phenoxasulfone, lancotrione sodium salt, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and phenoxasulfone is: Ratio of 1: 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10, and The mixing ratio with the lancotrione sodium salt is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10 by weight. The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10 by weight. More preferably 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, fentolazamide, lancotrione sodium salt, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and fentolazamide is 1 by weight. : 0.1 to 1: 150, preferably 1: 0.5 to 1:30, more preferably in the range of 1: 1 to 1:15, and the addition of fluropyroxifenebenzyl to lancotrione sodium salt The mixing ratio by weight is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10. The mixing ratio of piroxifene benzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably It is properly 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, pentoxazone, lancotrione sodium salt, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and pentoxazone is 1 by weight. : 0.04 to 1: 100, preferably 1: 0.2 to 1:20, more preferably 1: 0.4 to 1:10. And the mixing ratio by weight is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10, The mixing ratio of fluropyroxifene benzyl and propyrisulfuron is 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, in weight ratio. The Mashiku 1: 0.2 to 1: 5.

When the composition of the present invention is a composition containing fluropyroxifene benzyl, mefenacet, lancotrione sodium salt, and propyrisulfuron, the mixing ratio of fluropyroxifene benzyl and mefenacet is 1 by weight. : 0.2 to 1: 500, preferably 1: 1 to 1: 100, more preferably 1: 2 to 1:50, and the mixing ratio of fluropyroxifenebenzyl and lancotrione sodium salt Is in the range of 1: 0.05 to 1: 100, preferably 1: 0.25 to 1:20, more preferably 1: 0.5 to 1:10 by weight. The mixing ratio of phenbenzyl and propyrisulfuron is in a weight ratio of 1: 0.02 to 1:50, preferably 1: 0.1 to 1:10, more preferably 1: 0.2 to 1: 5.

  In the present invention, one or more compounds selected from the compound group A, one or more compounds selected from the compound group B, and fluropyroxifene benzyl are used by mixing with other herbicides as necessary. You can also. Further, it can be used in combination with insecticides, fungicides, plant growth regulators, fertilizers, safeners, soil improvers and the like.

  The composition of the present invention has herbicidal activity against a wide range of weeds, and is effectively effective in a wide range of crop fields, vegetable fields, paddy fields, orchards, or non-agricultural fields where normal tillage cultivation and non-tillage cultivation are performed. It is possible to control weeds, and no phytotoxicity is caused to the useful plants.

Examples of plants that can use the compound of the present invention include the following.
Agricultural crops: corn (horse-toothed, hard-grained, soft-grained, explosive, potato, sweet), rice (long, short, medium, japonica, tropical japonica, indica, javanica, paddy rice , Upland rice, floating rice, direct sowing, transplanting, sticky rice), wheat (bread wheat (hard, soft, medium, red wheat, white wheat), macaroni wheat, spelled wheat, club wheat, autumn sowing type, spring sowing type) , Barley (two-row barley (= beer wheat), six-row barley, hadakamugi, glutinous wheat, autumn sowing type, spring sowing type), rye (autumn sowing type, spring sowing type), rye wheat (autumn sowing type, spring sowing type) , Oat (autumn type, spring type), sorghum, cotton (upland type, pima type), soybean (infinite growth type, finite growth type, semi-finite growth type), groundnut (peanut), Saito ( Bean, lentil, azuki bean, cowpea, mung bean, Japanese bean, green bean, bamboo shoot, moss bean, tepary bean, broad bean, pea, chickpea, lentil, lupine, yellow bean, alfalfa, buckwheat, sugar beet, rapeseed, canola (spring sowing) Mold), sunflower, sugarcane, tobacco, etc.
Vegetables; Eggplant vegetables (eggplants, tomatoes, peppers, peppers, bell peppers, potatoes, etc.), cucurbits vegetables (cucumbers, pumpkins, zucchini, watermelons, melons, squash, etc.), cruciferous vegetables (radish, turnip, horseradish, Kohlrabi, Chinese cabbage, cabbage, mustard, broccoli, cauliflower, etc.), Asteraceae vegetables (burdock, shungiku, artichoke, lettuce, etc.), Lily family vegetables (eg, leek, onion, garlic, asparagus, etc.), Aceraceae vegetables (carrot, parsley) , Celery, American Bow Fu, etc.), red crustacean vegetables (spinach, chard, etc.), persimmon vegetables (perilla, mint, basil, lavender, etc.), strawberry, sweet potato, yam, taro, etc.
Fruit trees; pears (apples, pears, Japanese pears, quince, quince, etc.), nuclear fruits (peaches, plums, nectarines, ume, sweet cherry, apricots, prunes, etc.), citrus (satsuma mandarin, orange, lemon, lime, grapefruit) ), Nuts (chestnut, walnut, hazel, almond, pistachio, cashew nut, macadamia nut, etc.), berries (blueberry, cranberry, blackberry, raspberry, etc.), grape, oyster, olive, loquat, banana, coffee, Date palm, coconut palm, etc.
Others: tea, mulberry, flowering trees, roadside trees (ash, birch, dogwood, eucalyptus, ginkgo, lilac, maple, oak, poplar, redwood, fu, sycamore, zelkova, blackfish, Japanese amberjack, Tsuga, rat, pine, spruce, yew ), Flower buds, foliage plants, ferns, pastures.

  Examples of the non-agricultural land in the present invention include a playground, a vacant land, a track end, a park, a parking lot, a road end, a riverbed, under a power transmission line, a residential land, and a factory site.

  The crop cultivated in the crop field, vegetable field and paddy field in which the composition of the present invention is used is not limited as long as it is a variety cultivated generally as a crop.

  The aforementioned plants may be plants that can be produced by natural mating, plants that can be generated by mutation, F1 hybrid plants, and transgenic plants (also referred to as genetically modified plants). These plants generally have resistance to herbicides, accumulation of toxic substances against pests (also called pest resistance), suppression of susceptibility to diseases (also called disease resistance), increased yield potential, biological and abiotic It has characteristics such as improved resistance to stress factors and quality modification of the product (for example, increase / decrease in the content of specific components, change in composition, improvement in storage stability or workability)

  An F1 hybrid plant is a first-generation hybrid obtained by crossing two varieties of varieties, and is generally a plant having characteristics of hybrid strength having a trait superior to both of parents. Transgenic plants have characteristics that cannot be easily obtained by cross breeding, mutagenesis or natural recombination in the natural environment by introducing foreign genes from other organisms such as microorganisms. It is a plant that has been granted.

Examples of the technique for producing the above-mentioned plant include conventional breed improvement techniques; gene recombination techniques; genome breeding techniques; new breeding techniques; genome editing techniques. The conventional breed improvement technique is a technique for obtaining a plant having desirable properties by mutation or crossing. Genetic recombination technology is a technology that gives a new property to a living organism by removing the target gene (DNA) from a living organism (for example, a microorganism) and introducing it into the genome of another target organism, or a plant. Antisense technology or RNA interference technology that confer new or improved properties by silencing other genes present. The genome breeding technique is a technique for improving the efficiency of breeding using genome information, and includes a DNA marker (also referred to as genome marker or gene marker) breeding technique and genomic selection. For example, DNA marker breeding is a method in which a progeny having a target useful trait gene is selected from a large number of mating progenies using a DNA marker that is a DNA sequence that serves as a marker of the location of a specific useful trait gene on the genome. is there. By analyzing the progeny of mating using a DNA marker when the seedling is a young plant, the time required for breeding can be effectively shortened.
Genomic selection is a technique that creates prediction formulas from previously obtained phenotypes and genome information, and predicts characteristics without evaluating phenotypes from prediction formulas and genome information, contributing to efficient breeding. It is possible technology. New breeding techniques is a general term for breeding (breeding) techniques combining molecular biological techniques. For example, cisgenesis / intragenesis, oligonucleotide-directed mutagenesis, RNA-dependent DNA methylation, genome editing, grafting to GM rootstock or hogi, reverse breeding, agroinfiltration, seed production technology (Seed Production) Technology such as Technology, SPT). The genome editing technique is a technique for converting genetic information in a sequence-specific manner, and can delete base sequences, replace amino acid sequences, introduce foreign genes, and the like. Examples of such tools include zinc finger nuclease capable of sequence-specific DNA cleavage (Zinc-Finger, ZFN), Talen (TALEN), Crisper Cassine (CRISPR / Cas9), Crisper CPF1 (CRISPER / Cpf1) And meganuclease. In addition, there are sequence-specific genome modification techniques such as CAS9 nickase and Target-AID created by modifying the above-described tools.

  Examples of the above-mentioned plants include, for example, genetically modified crops in the electronic information site (http: // www. Plants listed in the registration database (GM APPROVAL DATABASE) are listed. More specifically, for example, herbicide-tolerant plants, pest-resistant plants, disease-resistant plants, product quality modification (for example, increase / decrease in content of components, change in composition, improvement in preservability or processability) And dwarf trait-modified plants, abiotic stress-tolerant plants, or plants with traits that are related to growth or yield.

Examples of plants given herbicide tolerance are listed below.
Mechanisms of resistance to herbicides, for example, reduce the affinity between herbicides and their targets; rapid metabolism of herbicides (such as degradation and modification) by the expression of enzymes that inactivate herbicides; Inhibition of uptake into plants; and inhibition of transfer of herbicides in plants.

Plants to which herbicide tolerance has been imparted by genetic recombination techniques include, for example, protoporphyrinogen oxidase (hereinafter abbreviated as PPO) herbicides such as flumioxazin; 4-hydroxyphenylpyruvic acid such as isoxaflutol and mesotrione Inhibitors of dioxygenase (hereinafter abbreviated as HPPD); imidazolinone herbicides such as imazetapil; acetolactate synthase (hereinafter abbreviated as ALS) inhibitors such as sulfonylurea herbicides such as thifensulfuronmethyl; glyphosate and the like 5-enol pyruvylshikimate-3-phosphate synthase (hereinafter abbreviated as EPSPS) inhibitor; glutamine synthetase inhibitor such as glufosinate; auxin type herbicide such as 2,4-D and dicamba; There are plants with tolerance to oxynyl herbicides. Preferred herbicide-tolerant transgenic plants are wheat such as wheat, barley, rye, oat, canola, sorghum, soybean, corn, cotton, rice, rapeseed, sugar beet, sugar cane, grape, lentil, sunflower, alfalfa, pome , Fruits, coffee, tea, strawberry, buckwheat, tomato, potato, cucumber, lettuce and other vegetables, more preferably wheat, barley, rye, oats, wheat, soybean, corn, rice, grape, tomato, Potato, pear.
The specific herbicide-tolerant plants are shown below.
Glyphosate herbicide-tolerant plants: glyphosate-tolerant EPSPS gene (CP4 Epps) derived from Agrobacterium tumefaciens strain CP4, modified from Bacillus licheniformis acetylphosphorifos N-acetyltransferase gene (gat4601 or gat4621), glyphosate oxidase gene (goxv247) derived from Ochrobacterum anthropi strain LBAA, or glyphosate resistant mutation derived from maize (Zea mays) Obtained by introducing any one or more of the S gene (mEPSPS or 2mepsps). The main plants are, for example, alfalfa (Medicago sativa), Argentine canola (Brassica napus), cotton (Gossypium hirsutuma L), creeping bentgrass (Agrostis stonifera), corn (Zea mais ras p. Examples include potato (Solanum tube HDDrosum L.), soybean (Glycine max L.), sugar beet (Beta vulgaris) and wheat (Triticum aestivum). Several glyphosate-tolerant plants are commercially available. For example, genetically modified plants into which CP4 epsps have been introduced have trade names including “Roundup Ready (registered trademark)”, and genetically modified plants into which gato 4601 or gata4621 have been introduced include “Optimum GAT (trademark)” and “Optimum (registered trademark). ) Glycanola ”and other genetically modified plants into which mepsps or 2 mepsps has been introduced are sold under the brand name“ GlyTol ™ ”. More specific glyphosate-tolerant plants include, for example, “Roundup Ready ™ Maize”, “Roundup Ready ™ 2 Maize”, “Agrisure ™ GT”, “Agrisure ™ GT / CB / LL "," Agriure (TM) GT / RW "," Agriure (TM) 3000GT "," YieldGard (TM) VT (TM) Rootworm (TM) RR2 "and" YieldGard (TM) VT Triple ";"Ready (TM) Soybean" and "Optimum GAT (TM)"; Cotton is "Roundup Ready (TM) Cotton", "Roundup Ready (TM) Flex Co tton "and" GlyTol (TM) ";Canola" Roundup Ready (TM) Canola "and" Optimum (R) Gly canola ";Alfalfa" Roundup Ready (TM) Alfa ";Rice"Roundup; Sugar cane is sold under the trade names "Roundup Ready (TM) sugarbeet" and "InVigor (TM) sugarbeet"; Wheat (Triticum aestivum) "Roundup Ready (TM) wheat".
Glyphosate herbicide-tolerant plant: phosphinothricin N-acetyltransferase (hereinafter abbreviated as PAT) gene of Streptomyces hygroscopicus PAT gene (pat) derived from Mogenes (Streptomies viridochromogenes) or any one of the PAT genes stipulated from Streptomyces viridochromogenes strain Tu494 (Streptomyces viridomochromogens strain Tu494). It is obtained by introducing. As main plants, for example, Argentine canola (Brassica napus), chicory (Cicorium intybus) cotton (Gossypium hirsutum L.), maize (Zea mays L.), polish canola (Brassica rapa, aa. (Glycine max L.) and sugar beet (Beta vulgaris). Some glufosinate-tolerant plants are commercially available. For example, transgenic plants introduced with bar or pat are sold under the trade names of “LibertyLink ™”, “InVigor ™”, or “WideStrike ™”. More specific glyphosate-tolerant plants include, for example, “Roundup Ready ™ 2”, “Liberty Link ™”, “Herculex ™ I”, “Herculex RW”, “Herculex XTRA ™”. , “Agriure ™ GT / CB / LL”, “Agriure ™ CB / LL / RW” and “Bt10”; Cotton “FiberMax ™ Liberty Link ™”; Rice “Liberty Link ™” ) Rice ”; Canola is sold under the trade name“ inVigor ™ Canola ”; Soybean is“ Liberty Link ™ Soybean ”; Sugar cane is sold under the trade name“ Liberty Link ™ sugarbeet ” .
Oxynyl herbicide (eg, bromoxynil) resistant plant: obtained by introducing a nitrilase gene (bxn) derived from Klebsiella pneumoniae subsp. Ozaenae. Major plants include, for example, Argentine canola (Brassica napus), cotton (Gossypium hirsatum L.), and tobacco (Nicotiana tabacum L.). Several oxynyl herbicide resistant plants are commercially available. For example, it is sold under the trade name including “Navigator ™” or “BXN ™”. As more specific oxynyl herbicide-tolerant plants, for example, cotton is sold under the trade name “BXN ™ Cotton”; Argentine canola is sold under the trademark “Navigate ™ Cotton”.
ALS herbicide-tolerant plants: Carnations (Dianthus caryophyllus) introduced with ALS herbicide-tolerant ALS gene (surB) derived from tobacco (Nicotiana tabacum) as selection markers include, for example, “Monudust (trademark)” and “Mononshadow (trademark)” , "Moonshade (TM)", "Moonlite (TM)", "Moonaqua (TM)", "Moonvista (TM)", "Mounique (TM)", "Moonepearl (TM)", "Moonberry (TM)" Alternatively, it is sold under the trade name “Moonvelvet ™”. Lick (Linum usitistisumum L.) introduced with an ALS herbicide-resistant ALS gene (als) derived from Arabidopsis thaliana is marketed under the trade name of “CDC Trifid Flax”, for example. Maize (Zea mays L.) that is resistant to sulfonylurea and imidazolinone herbicides introduced with corn-derived ALS herbicide-resistant ALS gene (zm-hra) is a trademark of “Optimum GAT (trademark)”, for example. It is sold by name. Soybean having resistance to an imidazolinone-based herbicide into which an ALS herbicide-resistant ALS gene (csr1-2) derived from Arabidopsis thaliana has been introduced is marketed under the trade name “Cultivance”, for example. Soybeans into which an ALS herbicide-tolerant ALS gene (gm-hr) derived from soybean (Glycine max) has been introduced are, for example, trademarks of “Treus (trademark)”, “Plenish (trademark)” and “Optimum GAT (trademark)”. It is sold by name. In addition, there is a cotton in which an ALS herbicide-resistant ALS gene (S4-HrA) derived from tobacco (Nicotiana tabacum cv. Xanthi) has been introduced.
HPPD herbicide-tolerant plant: obtained by introducing an HPPD gene (avhppd-03) derived from oat (Avena sativa). For example, a soybean introduced with a PAT gene (pat) derived from Streptomyces viridochromogenes at the same time as the above gene is a soybean having resistance to mesotrione and glufosinate as “Herbidide-tolerant Soybean line”. It is sold under the trade name.
2,4-D-tolerant plant or ACCase herbicide-tolerant plant: 2 introduced with an allyloxyalkanoate dioxygenase gene (aad-1) derived from Sphingobium herbicidovorans , 4-D or ACCase herbicide resistant corn is sold, for example, under the trade name “Enlist ™ Maize”. Soybeans and cottons that are resistant to 2,4-D or ACCase herbicides introduced with the allyloxyalkanoate dioxygenase gene (aad-12) from Delftia acidovorans are known, for example, It is sold under the trade name “Enlist ™ Soybean”.
Dicamba herbicide-tolerant plant: obtained by introducing a dicamba monooxygenase gene (dmo) derived from Stenotrophomonas maltophilia strain DI-6. Soybean and cotton into which the above gene has been introduced are known. A soybean (Glycine max L.) into which a glyphosate-resistant EPSPS gene (CP4 epsps) derived from Agrobacterium tumefaciens strain CP4 (Agrobacterium tumefaciens strain CP4) was introduced simultaneously with the above gene is, for example, “Genuity (registered trademark) u”. It is sold under the trade name “Ready ™ 2 Xtend ™”.
Additional plants with altered herbicide tolerance are widely known, such as alfalfa, apple, barley, eucalyptus, flax, grape, lentil, rapeseed, pea, potato, rice, sugar beet, which are resistant to glyphosate. Sunflower, tobacco, tomato beetle and wheat (see, eg, US 5188642, US 4940835, US 5633435, US 5804425, US 5627061); bean, cotton, soybean, pea, potato, sunflower, tomato, tobacco, resistant to dicamba Corn, sorghum and sugarcane (see for example WO 2008/051633, US 7105724 and US 5670454); soybean, sugar beet, potato resistant to glufosinate , Tomatoes and tobacco (see for example US 6376754, US 5646024, US 5561236); cotton, peppers, apple, tomato, sunflower, tobacco, potato, corn, cucumber, wheat, soybean, resistant to 2,4-D Sorghum and millet (see, for example, US61513401, US61000446, WO2005 / 107437, US5608147 and US5670454); canola having resistance to ALS-inhibiting herbicides (eg, sulfonylurea or imidazolinone herbicides), corn , Millet, barley, cotton, mustard, lettuce, lentil, melon, millet, oat, nata, potato, rice, rye, sorghum, soybean, sugar beet, sunflower Tobacco, tomato and wheat (see, for example, US5013659, WO2006 / 060634, US4761373, US5304732, US621114, US621114, and US62222100), particularly rice having resistance to imidazolinone herbicides, and acetolactate synthesizing genes ( rice having a specific mutation (for example, S653N, S654K, A122T, S653 (At) N, S654 (At) K, A122 (At) T) (see, for example, US2003 / 0217381, WO2005 / 020673); HPPD-inhibiting herbicides (for example, isoxazole herbicides such as isoxaflutol; triketone herbicides such as sulcotrione and mesotrione) And barley, sugarcane, rice, corn, tobacco, soybean, cotton, rapeseed, sugar beet, wheat and potato (eg, WO2004) that are resistant to diketonitrile, a degradation product of isoxaflutole such as pyrazoline. / 055191, WO1996 / 38567, WO1997 / 049816 and US6791014); and wheat, soybean, cotton, sugar beet, rapeseed, rice, corn, sorghum, sugar cane and sugar beet resistant to PPO-inhibiting herbicides (eg, US2002) / 0073443, US2008 / 0052798, Best Management Science, 61, 2005, 277-285).

  As plants to which herbicide tolerance has been imparted by conventional cultivar improvement technology or genome breeding technology, for example, rice “Clearfield (registered trademark) Rice having resistance to imidazolinone-based ALS-inhibiting herbicides such as imazetapil and imazamox. ”Wheat“ Clearfield® Wheat ”, sunflower“ Clearfield® Sunflower ”, lentil“ Clearfield® lentils ”and canola“ Clearfield® canola ”(BASF Ron; Soybean "STS soybean" resistant to sulfonylurea ALS-inhibiting herbicides such as methyl; trion oxime herbicides, aryloxyphenoxypropionic acid herbicides Corn “SR corn” (also known as “Poost Protected® corn”) resistant to acetyl-CoA carboxylase inhibitors of the sunflower “ExpressSun (registered trademark) sunflower resistant to sulfonylurea herbicides such as tribenuron ) ”; Rice“ Provisia ™ Rice ”resistant to acetyl CoA carboxylase inhibitors such as quizalofop; and canola“ Triazine Tolerant Canola ”resistant to photosystem II inhibitors; resistant to imidazolinone herbicides Sorghum “Igrowth ™” may be mentioned.

  Canola “SU Canola (registered trademark)” having sulfonylurea herbicide resistance using rapid cultivar development technology (Rapid Trait Development System, RTDS (registered trademark)) as a plant to which herbicide tolerance has been imparted by genome editing technology Is mentioned. RTDS (registered trademark) corresponds to oligonucleotide-directed mutagenesis in genome editing technology, and is a gene repair oligonucleotide (GRON), that is, cleaving DNA in plants via a DNA and RNA chimeric oligonucleotide. It is a technology that can introduce mutations without any problems. Other examples include maize with reduced herbicide tolerance and phytic acid content by deleting the endogenous gene IPK1 using zinc finger nuclease (see, eg, Nature 459, 437-441 2009); Rice that has been given herbicide tolerance using cast nine (see, for example, Rice, 7, 5 2014).

Examples of plants to which herbicide tolerance has been imparted by the new breeding technology include soybeans in which the properties possessed by GM rootstock are imparted to hogi using a variety improvement technology using grafts. Specific examples include soybeans (see Weed Technology 2013, 27, 412) that imparted glyphosate tolerance to non-transgenic soybean spikelets using Roundup Ready (registered trademark) soybean having glyphosate tolerance as rootstocks. .

  Examples of plants imparted with pest resistance are listed below.

Examples of plants that have been given resistance to lepidopteran pests by genetic recombination technology include, for example, delta-endotoxin (δ-endotoxin) that is an insecticidal protein derived from soil bacteria Bacillus thuringiensis (hereinafter abbreviated as Bt fungus). Maize (Zea mays L.), soybean (Glycine max L.), cotton (Gossypium hirsutum L.), rice (Oryza sativa L.), poplar (Populus sp.), Tomato (Lycopes) introduced with the gene to be encoded. , Eggplant (Solanum melongena) and sugar cane (Saccharum sp.). Examples of delta-endotoxins that confer resistance to lepidopteran pests include, for example, Cry1A, Cry1Ab, modified Cry1Ab (partially deleted Cry1Ab), Cry1Ac, Cry1Ab-Ac (a hybrid protein in which Cry1Ab and Cry1Ac are fused), Cry1C, Cry1F, Cry1Fa2 (modified cry1F), moCry1F (modified Cry1F), Cry1A. 105 (hybrid protein in which Cry1Ab, Cry1Ac and Cry1F are fused), Cry2Ab2, Cry2Ae, Cry9C, Vip3A and Vip3Aa20.
Examples of plants imparted with resistance to Coleoptera by genetic recombination technology include corn and potato introduced with a gene encoding delta-endotoxin, an insecticidal protein derived from soil bacteria Bt. . Examples of delta-endotoxins that confer resistance to Coleoptera include Cry3A, mCry3A (modified Cry3A), Cry3Bb1, Cry34Ab1, Cry35Ab1, Cry6A, Cry6Aa and mCry6Aa (modified Cry6Aa).
Examples of plants having resistance to Diptera pests by gene recombination technology include, for example, maize introduced with a synthetic gene encoding hybrid protein eCry3.1Ab fused with Cry3A and Cry1Ab derived from soil bacteria Bt (Zea mays L.) and cotton (Gossypium hirsutum L.) introduced with a gene encoding a trypsin inhibitor CpTI derived from cowpea (Vigna unguicula). Furthermore, there are poplars and the like into which an API encoding API, which is a protease inhibitor protein A derived from sage (Sagitaria sagittifolia), and exhibits resistance to a wide range of pests.
Insecticidal proteins that impart pest resistance to plants include hybrid proteins of the above insecticidal proteins, partially missing proteins, and modified proteins. The hybrid protein is produced by a combination of different domains of a plurality of insecticidal proteins using genetic recombination techniques, Cry1Ab-Ac and Cry1A. 105 etc. are known. As a protein lacking a part, Cry1Ab and the like lacking a part of the amino acid sequence are known. Examples of the modified protein include proteins in which one or more amino acids of the natural delta-endotoxin are substituted, and Cry1Fa2, moCry1F, mCry3A, and the like are known. The modified protein includes a case where a non-naturally occurring proteolytic enzyme recognition sequence is inserted into the toxin. For example, Cry3A055 (WO2003 / 018810 in which a cathepsin G-recognition sequence is inserted into the Cry3A toxin is used. Reference).
Cotton (event MON88702) introduced with modified BT protein Cry51Aa2 (Cry51Aa2.834_16) by gene recombination technology has been developed by Monsanto, and the genus Lymus, such as Lygus lineolaris, Hemiptera such as aphids, and Franklinella Resistant to thrips such as genus species.
In addition, as insecticidal proteins that impart pest resistance to plants by genetic recombination techniques, for example, insecticidal proteins derived from Bacillus cereus or Bacillus popillie; plant insecticidal proteins Vip1, Vip2 , Vip3 (Vip3Aa to Vip3Aj, Vip3Ba, Vip3B and Vip3Ca are known as subclasses, specifically, for example, Vip3Aa20 and Vip3Aa61 are known) and Vip4; Photolabda luminescence (Photerhabdus etc.) Photorhabdus spp. Or Xenolabdus nematophilus (Xenorhabdus nemat) Insecticidal proteins derived from nematode symbiotic (colonizing nematodes) bacteria such as philus, etc .; produced by animals containing insect-specific neurotoxins such as scorpion toxin, spider toxin, bee toxin, etc. Toxins produced by filamentous fungi such as Streptomyces venom; plant lectins such as pea lectin, barley lectin, snowdrop lectin; agglutinin; trypsin inhibitor, serine protease inhibitor, patatin, cystatin, Protease inhibitors such as papain inhibitors; Ribosome inactivating proteins (RIP) such as ricin, corn-RIP, abrin, ruffin, saporin, bryodin; 3-hydroxysteroid Steroid metabolic enzymes such as sidase, ecdysteroid-UDP-glucosyltransferase, cholesterol oxidase; ecdysone inhibitor; HMG-CoA-reductase; ion channel inhibitor such as sodium channel inhibitor, calcium channel inhibitor; juvenile hormone esterase; Diuretic hormone receptors; stilbene synthase; bibenzyl synthase; chitinase; and glucanase.

In addition, plants that have been imparted with pest resistance by introducing one or more insecticidal protein genes are already known, and some plants are commercially available.
As an example of cotton imparted with pest resistance, “Ballgard ™ cotton”, “BXN ™ Plus Bollgard ™ Cotton”, “BXN ™ Plus” expressing the insecticidal protein Cry1Ac derived from Bt bacteria “Bollgard ™ Cotton”, “JK 1”, “Roundup Ready ™ Bollgard ™ Cotton” and “Ingard ™”; “Herculex (Cry1Fa2)” expressing the insecticidal protein modified Cry1F (Cry1Fa2) from Bt bacteria "I" and "Herculex ™ CB";"VIPOT ™ Coton" expressing the insecticidal protein Vip3A from Bt; insecticidal proteins Cry1Ac and Cry2A from Bt "Bollgard II (trademark) cotton", "Roundup Ready (trademark) Bollgard II (trademark) Cotton", "Roundup Ready (trademark) Flex (trademark) Boldgard II (trademark) Coton" Link ™ Bollgard II ™ ”;“ Bollgard III ™ ”and“ Bollgard ™ III x Roundup Ready ™ ”expressing the insecticidal proteins Cry1Ac, Cry2Ab and Vip3A from Bt bacteria "VIPCOT ™ Roundup Read" expressing the insecticidal proteins Vip3A and Cry1Ab from Bt bacteria “Flex ™ Cotton”; “VIPOT® Cotton” expressing the insecticidal proteins Vip3A and Cry1Ac from Bt bacteria; “WideStrike ™ Cotton” expressing the insecticidal proteins Cry1Ac and Cry1F from Bt bacteria, “WideStrike ™ Roundup Ready ™ Coton” and “Widestrike ™ Roundup Ready Flex ™ Coton”; “TwinLk” and “TwinLk” that express the insecticidal proteins Cry1Ab and Cry2Ae from Bt bacteria (Trademark) x Twinlink (trademark) "; expressing insecticidal proteins Cry1Ac, Cry1F and Vip3A from Bt bacteria "Widestrike (TM) 3" and "Widestrike (TM) x Roundup Ready Flex (TM) x VIPCOT (TM) Coton"; the trademarks expressing the insecticidal proteins Cry1Ab, Cry2Ae and Vip3A from Bt x Twinlink (TM) x VIPCOT (TM) Cotton ", which are commercially available.
Examples of corn imparted with pest resistance include “YieldGard® Rootworm RW”, “YieldGard ™ RW + RR”, “YieldGard ™ VT” expressing the insecticidal protein Cry3Bb1 derived from Bt bacteria. (Trademark) Rootworm (TM) RR2 "and" MaxGard (TM) ";" YieldGard (R) VT Triple "and" YieldGard (TM) Plus R "expressing the insecticidal proteins Cry3Bb1 and Cry1Ab from Bt bacteria; “Bt Xtra ™ Maize” expressing the insecticidal protein Cry1Ac derived from fungi; “YieldGar” expressing the insecticidal proteins Cry1Ab and Cry3Bb1 derived from Bt fungi Plus® ”;“ Bt10 ”,“ Liberty Link ™ Yieldgard ™ Maize ”,“ Agrisure ™ GT / CB / LL ”and“ Yieldgard ”expressing the insecticidal protein Cry1Ab from Bt bacteria (Trademark) CB + RR "; insecticidal protein Cry1A. “YieldGard ™ VT Pro ™” and “Genuity ™ VT Double Pro ™” expressing 105 and Cry2Ab2; “Agriure ™ RW” expressing the insecticidal protein mCry3A from Bt bacteria ”And“ Agrisure ™ GT / RW ”;“ Starlink ™ Maize ”expressing the insecticidal protein Cry9C from Bt;“ Yieldgard ™ ”expressing the insecticidal protein Cry1Ab from Bt “MaizeGard ™”, “NaturGard KnockOut ™”, “Maximizer ™”, “Roundup Ready ™” YieldGard ™ “mize”, “Agri” ure (TM) CB / LL "and" Mavera (TM) YieldGard (TM) Maize ";" Agrisure (R) 3 "expressing the insecticidal proteins Cry1Ab, Cry1F, modified Cry3A, Cyr34Ab1 and Cyr35Ab1 from Bt bacteria “Agriure® Viptera” expressing the insecticidal protein Vip3Aa20 from Bt bacteria; “Agriure® Viptera ™ 2100” and “Agrisure®” expressing the insecticidal proteins Vip3Aa20 and Cry1Ab from Bt bacteria (Trademark) Viptera (trademark) 3110 ";" Agris "expressing the insecticidal proteins Vip3Aa20, Cry1Ab and modified Cry3A from Bt bacteria ure (R) Viptera (TM) 3100 "," Agriure (R) Viptera (TM) 3111) and "Agriure (R) Viptera (TM) 4"; insecticidal protein Vip3Aa20, Cry1Ab and modifications from Bt “Agriure® Viptera® 3220” expressing Cry1F; “Agriure® Duracade®” expressing the insecticidal protein eCry3.1Ab (a chimeric protein of Cry3A-Cry1Ab) from Bt bacteria; Bt bacteria-derived insecticidal protein eCry3.1Ab (a chimeric protein of Cry3A-Cry1Ab), modified Cry3A, Cry1Ab and modified Cry1F ure® Duracade ™ 5122 ”; an insecticidal protein eCry3.1Ab (Cry3A-Cry1Ab chimeric protein) from Bt,“ Agriure® Duracade ”that expresses the modified Cry3A, modified Cry1Ab and Vip3A variants (Trademark) 5222 ";" Herculex (trademark) RW "expressing insecticidal proteins Cyr34Ab1 and Cyr35Ab1 derived from Bt bacteria; Insecticidal protein Cry1A. 105, “Genuity® VT Triple Pro ™” expressing Cry2Ab2 and Cry3Bb1; insecticidal proteins Cry1F, Cry2Ab, Cyr34Ab1, Cyr35Ab1, Cry3Bb1 and Cry1A. "Genuity (R) SmartStax (TM)" which expresses 105; insecticidal protein modified Cry1F, Cry2Ab and Cry1A. “Power Core ™” expressing 105; “Herculex XTRA ™ RR” expressing insecticidal protein-modified Cry1F, Cyr34Ab1 and Cyr35Ab1 from Bt; insecticidal protein-modified Cry1F, Cyr34Ab1, Cyr35Ab1 from Bt "Optimum (registered trademark) Intranct Xtreme" expressing Cry1Ab and Cry1Ab; Insecticidal protein modified Cry1F, Cyr34Ab1, Cyr35Ab1 and Cry1Ab derived from "Optimum (registered trademark) InttractBTRXTR; And “Optimum® TRIsect” expressing the insecticidal protein modified Cry1F and modified Cyr3A. Commercially available.
Examples of other pest-resistant plants include potatoes “Atlantic NewLeaf (trademark) potato”, “NewLeaf (trademark) Russet Burbank potato”, “Lugovsku”, “Lugovsk”, which express the insecticidal protein Cry3A derived from Bt bacteria. "Elizaveta plus", "Hi-Lite NewLeaf (trademark) Y potato, Superior NewLeaf (trademark) potato" and "Shepody NewLeaf (trademark) Y crot protein". 63 "and" Huahui-1 ";soybean" Intacta ™ "expressing the insecticidal protein Cry1Ac from Bt bacteria Roundup Ready (trademark) 2 Pro ”; eggplant“ BARI Bt Begun-1, −2, −3 and −4 ”expressing the insecticidal protein Cry1Ac derived from Bt bacteria, and these are commercially available.
Also, corn “Yield corn rootworm”, “Yieldgard VT”, “Herculex RW”, “Herculex Rootworm” and “Agrisure CRW” having resistance to corn rootworms; , "Yieldgard plus", "Yieldgard VT Pro", "Agriure CB / LL", "Agriure 3000GT", "Hercules I", "Hercules II", "KnockOut", "NatureGartL" , Corn borer, black cut worm and faller Maize with resistance to worms “Herculex I”, “Herculex Xtra”, “NewLeaf”, “NewLeaf Y” and “NewLeaf Plus”; Corn with resistance to corn borers and corn rootworms “YieldGard Plus”; Cotton "Ballgard I" and "Bollgard II" resistant to tobacco moth; Cotton "Bollgard" resistant to fake American tobacco, cotton ball worm, fall army worm, beet army worm, cabbage looper, soybean looper and pink ball worm II "," WideStrike ™ "and" VipCot "; tobacco tin mega-resistant potato" ”newLeaf”, “NewLeaf Y” and “NewLeaf Plus”; eggplants “Bt brinjal”, “Dumaguete Long Purple” and “Mara” (see, eg, US5128130) with resistance to eggplant moths, fruit bowlers and cotton ball worms. ing.
Additional plants with pest resistance are generally known, for example, corn borer resistant rice (see, eg, Molecular Breeding, Vol. 18 (2006), No. 1), lepidopterous resistant lettuce (eg, US5349124), and rice (for example, see WO2001 / 021821) having resistance to Lepidoptera (for example, Nika maize, Ichimongiseseri, rice mushrooms, corn borer, rice case worm, and rice army worm). Methods for producing such plants are generally known to those skilled in the art and are described, for example, in the above publications.

  Plants that have been given pest resistance by RNA interference technology include lepidopterous pests (eg, cut worms such as corn borers, corn ear worms, black cut worms, and fall army worms) and Coleoptera pests (corn root worms) Maize that is resistant to) is marketed or developed under the trade names "SmartStarx (R)", "SmartStax (R) Pro" or "Genuity (R) SmartStax Pro".

Examples of plants imparted with pest resistance by conventional breeding techniques or genome breeding techniques include, for example, the aphid resistance gene “Rag1 (Resistance to Aphis glycines 1)” or “Rag2 (Resistance to Aphis glycines) 2) Soybean having resistance to soybean aphids having the gene (see J. Econ. Entomol., 2015, 108, 326.); Soybean having resistance to soybean cyst nematode (Heterodera glycines) (Phytopathology) , 2006, 106, 1444.); a resistance to resistance to Meloidogyne incognita. (J. Nematol, 2009, 41, 140.); Rice, "Kanto No. BPH1" that are resistant to the brown planthopper; and include soybean "Fukuminori" that are resistant to common cutworm.

  These pest-resistant plants are given resistance to any harmful insects (especially lepidopterous insects, Coleoptera insects, Diptera insects, Coleoptera insects), harmful spiders and harmful nematodes Has been. Plants imparted with pest resistance are preferably wheat (eg wheat, barley, rye, oat), corn, canola, sorghum, soybean, rice, rapeseed, sugar beet, sugarcane, grape, lentil, sunflower, alfalfa, Selected from berries, drupes, peanuts, coffee, tea, strawberries, turf, vegetables (eg tomatoes, potatoes, cucurbits and lettuce), more preferably soybean, corn, tomatoes, rice and wheat (E.g. wheat, barley, rye and oat), most preferably selected from soybeans, rice, corn and wheat (e.g. wheat, barley, rye and oat).

  Examples of plants imparted with disease resistance are listed below.

Plants to which disease resistance has been conferred by genetic engineering techniques, for example, express so-called “pathogenicity-related proteins” (PRP, see eg EP 0392225) or so-called “antifungal proteins” (AFP, see eg US 6686068) Plant. Various antifungal proteins with activity against phytopathogenic fungi have been isolated from specific plant species and are common sense. Examples of such anti-pathogenic substances and plants from which such anti-pathogenic substances can be synthesized are known, for example, from EP 0 392 225, WO 1993/05153, WO 1995/33818, and EP 0353191. Plants that are resistant to fungicidal pathogens, viral pathogens and bacterial pathogens are created by introducing disease resistance genes. A number of resistance genes have been identified and isolated and used to improve disease resistance, such resistance genes include, for example, producing tobacco mosaic virus (TMV) resistant tobacco plants N genes introduced into TMV-sensitive tobacco lines (see eg US Pat. No. 5,571,706), Prf genes introduced into plants to obtain enhanced pathogen resistance (see eg WO 1998/02545), And the Rps2 gene derived from Arabidopsis thaliana used to create resistance to bacterial pathogens such as Pseudomonas syringae (see, eg, WO 1995/028423). Plants exhibiting a systemic acquired resistance response were obtained by introducing a nucleic acid molecule encoding the TIR domain of the N gene (see, eg, US 6630618). Further examples of known resistance genes include the Xa21 gene that has been introduced into a number of rice varieties (see, eg, US5952485, US5974734, WO1999 / 009151, WO1996 / 022375), for the resistance to collectototrichum. Rcg1 gene (see, eg, US2006 / 225152), prp1 gene (see, eg, US5859332, WO2008 / 017706), ppv-cp gene that introduces resistance to plumpox virus (see, eg, US PP15,154Ps), In order to introduce resistance to the P1 gene (see for example US Pat. No. 5,968,828), potato phytophytoinfestans in potato Genes such as Blb1, Blb2, Blb3, RB2 and Rpi-vnt1 (see for example US Pat. No. 7,148,497), LRPKml gene (for example see WO 1999/064600), P1 gene for potato virus Y resistance (see eg US Pat. No. 5,968,828) ), HA5-1 gene (see for example US 5877403 and US 6046384), PIP for introducing broad resistance to viruses such as potato virus X (PVX), potato virus Y (PVY), potato cigar virus (PLRV) Genes (see eg EP0707079), and genes such as the Arabidopsis NI16, ScaM4 and ScaM5 genes for obtaining fungal resistance (eg For example, see US6706952 and EP1018553). In addition, bean golden mosaic virus (hereinafter referred to as BGMV) -resistant bean is a plant to which resistance has been imparted by RNA interference technology, and is a double-stranded RNA gene of a replication protein. (Sense and antisense ac1 gene) is introduced, and the synthesis of BGMV replication protein is inhibited to show resistance to BGMV. Methods for producing such plants are generally known to those skilled in the art and are described, for example, in the above publications.
Anti-pathogenic substances that can be expressed by such plants include, for example, ion channel blockers (sodium channel blockers, calcium channel blockers, etc.); viral KP1, KP4 and KP6 toxins; stilbene synthase; bibenzyl synthase Chitinase; glucanase; so-called “pathogenicity related proteins” (PRP; see eg EP 0392225); anti-pathogenic substances produced by microorganisms (eg peptide antibiotics, heterocyclic antibiotics (eg WO 1995/033818) And protein factors or polypeptide factors involved in plant pathogen defense (so-called “plant disease resistance genes” described in WO2003 / 000906)).
Anti-pathogenic substances produced by plants can protect plants from various pathogenic microorganisms such as fungi, viruses and bacteria. Useful plants of increasing interest in connection with the present invention are wheat (eg, wheat, barley, rye and oats), soybean, corn, rice, rapeseed, berries, nuclear fruits, peanuts, coffee, tea, strawberries. Vines and vegetables (eg tomatoes, potatoes), cucurbits, papayas, melons, lentils and lettuce, more preferably soybeans, tomatoes, rice and wheat (eg wheat, barley, Rye and oat), most preferably selected from soybeans, rice and wheat (eg wheat, barley, rye and oats).
Examples of plants having resistance to fungal pathogens include, for example, soybeans having resistance to soybean rust fungi (Phakopsora pachyrhizi and Phakopsora meibomiae) (see, for example, WO 2008/017706) or Eggplants such as cotton, tomato, potato, etc. that are resistant to (see, for example, US5859332, US7148397, EP1333499); maize that is resistant to genus Colletotrichum, such as Colletotrichum graminola 200 See / 225152 ); Apple scab (see apples (e.g. WO1999 / 064600 having resistance to Venturia inaequalis)); Fusarium (e.g., fusarium graminearum, fusarium sporotrichioides, fusarium lateritium, fusarium pseudograminearum, fusarium sambucinum, fusarium culmorum, fusarium poae Plants (eg, rice, wheat, barley, rye, corn, oat, potato, melon, soybean, and sorghum) that are resistant to fusarium accuminatum, fusarium equiseti) (eg, US 646184, see EP 1477557); plants such as corn, soybean, wheat (especially wheat, barley, rye and oat) rice, tobacco, sorghum, sugar cane, potato, etc. having a broad fungicidal resistance (eg US 58593332, US 5689046, U.S. Pat. No. 6,706,952, EP1018553 and U.S. Pat.
Examples of plants having resistance to bacterial pathogens include, for example, rice having resistance to xylella fastidiosa (see, for example, US Pat. No. 6,232,528); rice having resistance to bacterial head blight, cotton, Plants such as soybean, potato, sorghum, corn, wheat, barley, sugarcane, tomato and pepper (see, for example, WO2006 / 42145, US5952485, US5997434, WO1999 / 09151, WO1996 / 22375); Pseudomonas syringae Tomatoes having resistance (see, for example, Can. J. Plant Path., 1983, 5: 251-255).
Plants that are resistant to viral pathogens include, for example, nuclear fruits (eg, plum, almond, apricot, cherry, peach, nectarine) that are resistant to plum pox virus (eg, US PP15154Ps, Potato resistant to potato virus Y (see, for example, US Pat. No. 5,968,828); potato, tomato, cucumber resistant to tomato spotted wilt virus And plants such as legumes (see, for example, EP 0 626 449, US 5973135); resistance to maize streak virus Maize (see for example US 6040496); papaya with resistance to papaya ring spot virus (see eg S5877403, US 6046384); resistance to cucumber mosaic virus Cucurbitaceae plants (eg, cucumbers, melons, watermelons and pumpkins) and solanaceous plants (eg potatoes, tobacco, tomatoes, eggplants, paprikas, peppers and peppers) (see, eg, US68479780); watermelon mosaic virus 2) and resistance to zucchini yellow mosaic virus Cucurbitaceous plants having sex (eg cucumbers, melons, watermelons and pumpkins) (see eg US 6015942); potato cigar virus (potatoes having resistance to potato leafroll virus (see eg US 5576202); potato virus X (potato) Potatoes with broad resistance to viruses such as virus X), potato virus Y (potato virus Y), potato leafroll virus (see eg EP0707079); bean golden mosaic virus (Bean golden) kidney beans that are resistant to mosaic virus (eg, Mol Plant Microbe Inter) ct. 2007 Jun; 20 (6): 717-26. For example).
There are plants that are resistant to antibiotics (eg, kanamycin, neomycin and ampicillin). The naturally occurring bacterial nptII gene expresses an enzyme that blocks the action of the antibiotics kanamycin and neomycin. The ampicillin resistance gene ampR (also known as blaTEM1) is derived from the bacterium Salmonella paratyphi and is used as a marker gene in microbial and plant transformation. ampR is involved in the synthesis of beta-lactamase, an enzyme that neutralizes antibiotics of the penicillin family including ampicillin. Plants having resistance to antibiotics include, for example, potato, tomato, flax, canola, rapeseed, rape seed and corn (eg, Plant Cell Reports, 20, 2001, 610-615, Trends in Plant Science, 11, 2006, 317-319, Plant Molecular Biology, 37, 1998, 287-296, Mol Gen Genet., 257, 1998, 606-13. Plant Cell Reports, 6, 1987, 333-336, Fer Register (USA), 60, No. 113, 1995, 31139. Federal Register (USA), 67, No. 22 , 2002, 70392, Federal Register (USA), 63, No. 88, 1998, 25194, Federal Register (USA), 60, No. 141, 1995, 37870, Canadian Food Inspection Agency. FD / OFB-095-264-A, October 1999, FD / OFB-099-127-A, October 1999). Preferably, the plant is selected from soybeans, tomatoes and wheat (eg wheat, barley, rye and oats), most preferably selected from soybeans and wheat (eg wheat, barley, rye and oats). The
Examples of the plants imparted with resistance to available plant viral diseases include papaya “Rainbow”, “SunUp”, and “Huangong No. 1” imparted with resistance to papaya ringspot virus. Potatoes "Innate (R) Hibernate", "Innate (R) Glaciate" and "Innate (R) Acclimate" exhibiting resistance to potato phytopathogens; Potato virus Y and / or potato cigars Potato "Newleaf (TM)" showing resistance to virus (PLRV).

  As a plant imparted with disease resistance by conventional cultivar improvement technology or genome breeding technology, rice to which resistance to blast (blast) has been imparted; resistance to sheath blight (confection) Rice that has been rendered resistant to leaf rust; wheat that has been rendered resistant to stripe rust; wheat that has been rendered resistant to stem rust; Wheat imparted resistance to powdery mildew; Wheat imparted resistance to leaf blotch; Wheat imparted resistance to bacterial blotch; macular disease Wheat given resistance to (tan spot); Barley imparted resistance to powdery mildew; Barley imparted resistance to dwarf leaf rust; Barley imparted resistance to net blotch; Cloud disease Barley imparted resistance to (scald); Barley imparted resistance to Ramularia disease; Maize imparted resistance to anthracnose; Gray leaf spot disease ( Corn imparted resistance to gray leaf spot; Corn imparted resistance to Goss's wilt disease; Fusarium stalk rot (Fusarium) maize imparted resistance to talk rot; soybean imparted resistance to Asian soybean rust; soybean imparted resistance to phytophthora stem and root rot; suddenly Soybean conferred to resistance to death syndrome; Pepper conferred to resistance to Phytophthora rot; Lettuce conferred to powdery mildew; tomato resistant to bacterial wilt; tomato resistant to gemini virus; resistant to downy mildew Lettuce; rapeseed, cabbage, brussels sprouts, cauliflower, colored green (Borekale), broccoli and other cruciferous plants with resistance to clubroot; resistance to black leg Rapeseed, cabbage, Brussels sprouts, cauliflower, colored green (Borekale), broccoli, etc .; Fusarium oxysporum f. sp. The melon (for example, refer to WO2009 / 000736) imparted with resistance to Melonis caused by Melonis.

By using Talen and Crisper Cassine as a plant to which disease resistance has been imparted by genome editing technology, the powdery mildew disease resistance gene (MILDEW RESISTOR LOCUS O, hereinafter abbreviated as MLO) is deleted. Bread wheat resistant to disease (see, for example, Nat. Biotech., 32, 947-951 2014); deletion of the SlMLO1 gene, one of the MLOs, using crisper cassine , Slmlol tomato (Tomelo) resistant to powdery mildew (see, eg, Scientific Reports 7, Article number: 482, 2017); Rice (Nat. Biotechnol. 30, 390-392, 2012), which shows resistance to Xanthomonas oryzae pv. Oryzae causing bacterial leaf blight by editing the OsSWEET14 gene of Rice (PLoS ONE 11: e0154027. Doi: 10.1371 / journal.) Resistant to Magnaporthe oryzae causing blast disease by modifying the OsERF922 gene in rice using Nine. pone.0154027 2016); using recessive eIF4E (eukaryotic translation open) using crisper cassine. Factor 4E) Due to the disruption of the gene, cucumber vein yellow virus (CVYV), zucchini yellow mosaic virus (ZYMV), papaya ringspot virus-type W (PRSV-W) See 2016); soybeans that are resistant to phytophthora stem and root rot caused by Phytophthora sojae by disrupting the RXLR effector gene (Avr4 / 6) using Crisper Cassine 17 (1) 127-139 2016) It is.

  Introducing Rvi6 gene (previously called HcrVf2), which is resistant to apple mold caused by Venturia inaequalis, using cisgenesis as a plant to which disease resistance has been imparted by new breeding technology An apple that is resistant to apple mold (for example, see Plant Biotech. J., 12, 2-9, 2014); an example that gives sapling the properties of GM rootstock, which is a breeding technique using grafts As an example, a sweet cherry (Plant Biotech. J., 12, 1) whose properties have been transferred from a transgenic rootstock resistant to infection with the Prunus necrotic ringspot virus to a non-transgenic spikelet. 19-1328 see 2014), and the like.

Examples of plants with modified product quality are listed below.
The product quality modification means the synthesis of the modified component or the increase or decrease in the synthesis amount of the component compared to the corresponding wild type plant. Plants with modified product quality include, for example, modified plants with increased or decreased vitamin, amino acid, protein and starch, various oil content, and modified plants with reduced nicotine content.

  Plants whose product quality has been modified by genetic recombination technology include, for example, alfalfa-derived S-adenosyl-L-methionine: trans-caffeoyl CoA 3-methyltransferase (ccomt) gene duplexes involved in lignin production Alfalfa in which a gene that generates RNA is introduced and the lignin content is reduced by RNA interference action; a triacylglyceride containing lauric acid by introducing a 12: 0 ACP thioesterase gene derived from Laurier involved in fatty acid synthesis (Umbellularia californica) Increased content of canola “Laurical ™ Canola”; by introducing a partial gene (gm-fad2-1) of ω-6 desaturase derived from soybean, a fatty acid desaturase Soybean "Plenish (TM)" and "Treus (TM)" with suppressed expression of the gene and increased oleic acid content; Soybean-derived acyl-acyl carrier protein thioesterase gene (fatb1-A) duplex Soybean "Visible Gold (trademark)" in which the saturated fatty acid content is reduced by introducing a gene that generates RNA and a gene that generates double-stranded RNA of the soybean-derived δ-12 desaturase gene (fad2-1A); Transgenic soybean in which stearidonic acid, which is one of ω3 fatty acids, was produced by introducing a δ-6 desaturase gene (Pj.D6D) derived from Saccharomyces cerevisiae and a δ-12 desaturase gene (Nc.Fad3) derived from red bread mold; Thermococcus for starch degradation (Ther) maize “Enogen®” with enhanced production of bioethanol by introducing the thermostable alpha-amylase gene (amy797E) of Mococcales sp .; Corynebacterium glutamicum for the production of lysine, an amino acid Maize “Mavera ™ Maize” and “Mavera ™ YieldGard ™ Maize” with increased lysine production by introducing a dihydrodipicolinate synthase gene (cordapA) derived from potato; starch synthase from potato By introducing the antisense gene gbss of (granule-bound star synthase enzyme, GBSS) Potatoes “Amflora ™”, “Star Potato” with reduced amylose content and increased amylopectin content in starch granules; generate double-stranded RNA of transcription factor genes PhL and R1 that promote starch degradation from potato Inhibition of starch degradation by introducing the genes pPhL and pR1, and suppression of asparagine synthesis by introducing the gene asn1 that generates the double-stranded RNA of the gene Asn1 involved in asparagine production (production of acrylamide, a carcinogen by heating) Potato with reduced black spot formation by introducing the gene ppo5 that generates double-stranded RNA of the polyphenol oxidase gene Ppo5 derived from potato. "Crateate", "Innate (registered trademark) Generate", "Innate (registered trademark) Accelerate", "Innate (registered trademark) Invigorate", "Innate (registered trademark) Glaciate", "Innate (registered trademark) Accelerate" and "Innate" (Registered trademark) “Hibernate”; tobacco whose nicotine content was reduced by introducing an antisense gene (NtQPT1) of the quinolinate phosphoribosyltransferase gene QpTase from tobacco (Nicotiana tabacum); phyto from Narcissus pseudonarcissus Soil bacteria (E) that synthesizes a synthase gene (psi) and carotenoids Golden rice (Golden), which is a rice that can produce β-carotene in endosperm tissue and harvest rice containing vitamin A by introducing a carotene desaturase gene (crt1) derived from winia uredovora) and expressing it specifically in the endosperm. rice). Other examples include, for example, potato and corn with modified amylopectin content (see, for example, US6784338, US2007 / 0261136, WO1997 / 04471); canola, corn, cotton, grape, cattail with modified oil content , Cowpea, rice, soybean, rapeseed, wheat, sunflower, bittern, safflower and vernonia (e.g., U.S. Pat. / 079499, US2006 / 0075515 and US7294759); fatty acids included Sunflower with increased amount (see, eg, US6084164); soybean with reduced allergen content (see, eg, US68664362); tobacco with reduced nicotine content (see, eg, US2006 / 0185684, WO2005 / 000352 and WO2007 / 064636) Canola and soybean with increased lysine content (see, eg, Bio / Technology 13, 1995, 577-582); corn and soybean with modified methionine, leucine, isoleucine and / or valine compositions (eg, , US 6946589, US 6905877); soybeans with increased sulfur amino acid content (see for example EP0992985, WO 1997/041239); E. coli (Escherichia) 3) -phosphoadenosine-5′-phosphosulfate reductase (3′-phosphoadenosine-5′-phosphosulfate reductase) derived from E. coli was specifically expressed in the leaf surface, so that maize having an increased methionine content (PNAS, 2017, 114 (43), 11386.); free amino acids (eg asparagine, aspartic acid, serine, threonine, alanine, histidine and glutamic acid) content increased tomatoes (eg see US Pat. No. 6,727,411); amino acid content increased Corn (see for example WO05 / 077117); potatoes, corn and rice with modified starch content (see for example WO1997 / 044471 and US7317146); Tomatoes, corn, grapes, alfalfa, apples, legumes and peas with modified labnoid content (see for example WO 00/04175); corn, rice, sorghum, cotton and soybean with modified phenolic compound content (See, for example, US 2008/0235829); tomatoes and canola with increased vitamin A content (see, for example, US 6797498, US 7348167); tomatoes, canola, soybeans, wheat, sunflower, rice with increased vitamin E content Corn, barley and rye (see, for example, US7348167, WO2004 / 058934); alfalfa, apple, legume, corn, grape, tomato and pea with modified flavonoid content ( In example, see WO00 / 04175), and the like. Methods for producing such plants are generally known to those skilled in the art and are described, for example, in the above-mentioned publications. Preferably, the plant is selected from soybeans, canola, tomatoes, rice and the like (eg wheat, barley, rye and oats), most preferably selected from soybeans, canola, rice, wheat and barley.

  Rapeseed “Nexera (registered trademark) Canola” that produces unsaturated omega-9 fatty acids as a plant whose quality of the product has been modified by conventional breeding technology or genome breeding technology; soybean with reduced allergen content “Yumeminori”; rice for the purpose of changing to a good taste, for example, rice “Yumepirika” with a reduced amylose content is commercially available. Citrus with modified fruit characteristics (for example, fruit weight, fragrance, juiciness and sugar content) is known (see Scientific Reports 7, 4721 2017).

  Examples of plants that have modified the nutrient utilization of plants include plants in which assimilation or metabolism of nitrogen or phosphorus is enhanced. Plants having nitrogen assimilation ability and nitrogen utilization ability enhanced by genetic recombination technology include, for example, canola, corn, wheat, sunflower, rice, tobacco, soybean, cotton, alfalfa, tomato, wheat, potato, sugar beet, sugarcane and Rapeseed (see, for example, WO 1995/009911, WO 1997/030163, US6084153, US59555651, and US68664405). Plants with improved phosphorus uptake by genetic engineering techniques include, for example, alfalfa, barley, canola, corn, cotton, tomato, rapeseed, rice, soybean, sugar beet, sugar cane, sunflower, wheat and potato (e.g. US7417181, US2005 / 0137386). Methods for producing such plants are generally known to those skilled in the art and are described, for example, in the above-mentioned publications. Preferably, the plant is selected from soybeans, tomatoes and wheat (eg wheat, barley, rye and oats), most preferably selected from soybeans, rice, corn and wheat.

  Plants whose fertility traits and the like have been modified by gene recombination techniques include plants in which male sterility and fertility recovery traits have been imparted to plants. For example, maize and chicory imparted with male sterility by expressing a ribonuclease gene (barnase) derived from Bacillus amyloliquefaciens in cocoon tapetum cells; a DNA adenine methylase gene (dam) derived from E. coli Maize that has been given a male sterility trait by introduction of a maize-derived alpha-amylase gene (zm-aa1) that gives a male sterility trait and a maize-derived ms45 protein gene (ms45) that gives a fertility recovery trait Maize with controlled fertility traits by expressing a ribonuclease inhibitor protein gene (barstar) derived from Bacillus in tapetum cells of straw A canola that has been given a fertilizer; and a ribonuclease gene (barnase) derived from Bacillus giving a male sterility trait and a ribonuclease inhibitory protein gene (barstar) derived from Bacillus giving a fertility restoring trait are controlled Canola. Other plants to which fertile traits have been imparted by gene recombination techniques include tomato, rice, mustard, wheat, soybean, and sunflower (for example, US6720481, US6281348, US5659124, US6395956, US7345222, US7230168, US6072102, EP1135982, WO2001). / 092544 and WO 1996/040949). Methods for producing such plants are generally known to those skilled in the art and are described, for example, in the above-mentioned publications. Preferably, the plant is selected from corn, canola, soybean, rice, tomatoes and wheat grains (eg wheat), most preferably from corn, canola, soybean, rice, wheat.

  Plants with abiotic stress tolerance are limited to drought, high salinity, high light intensity, high UV irradiation, chemical contamination (eg high heavy metal concentrations), low or high temperature, nutrients (ie nitrogen, phosphorus) Plants exhibiting increased resistance to abiotic stress conditions such as supply and collective stress (see, for example, WO 2000/004173, WO 2007/131699, CA 2521729 and US 2008/0229448).

  Examples of plants imparted with abiotic stress tolerance by genetic recombination technology include rice, corn, soybean, sugarcane, alfalfa, wheat, tomato, potato, barley, rapeseed, legume, oat, sorghum that are resistant to drought. And cotton (see, for example, WO 2005/048693, WO 2008/002480 and WO 2007/030001); low temperature resistant corn, soybean, wheat, cotton, rice, rapeseed and alfalfa (see, eg, US4731499 and WO2007 / 112122) Rice, cotton, potato, soybean, wheat, barley, rye, sorghum, alfalfa, grape, tomato, sunflower and tobacco (e.g., US7256326, US70) resistant to high salinity 4139, see WO / 2001/030990), and the like. Further, there is a corn “DroughtGard (registered trademark)” (Monsanto product) into which a cold shock protein gene cspB of Bacillus subtilis is introduced.

  Examples of plants imparted with abiotic stress tolerance by conventional breeding techniques or genome breeding techniques include corn having drought tolerance (Agriure Artesian (registered trademark)) and "Optimum ( It has been developed under the trade name “registered trademark” AQUAmax (registered trademark) ”.

  Plants to which other characteristics are imparted include plants with modified maturation characteristics. Examples of alteration of maturation characteristics include delayed ripening, delayed softening and early maturation. As a plant whose maturation characteristics are modified by gene recombination technology, for example, by introducing an S-adenosylmethion hydrolase gene (sam-K) derived from E. coli bacteriophage T3 relating to ethylene production of a plant hormone, shelves can be stored. Improved melon and tomato; gene lacking part of ACC synthase gene derived from tomato involved in ethylene production of plant hormone, ACC deaminase gene derived from Pseudomonas chlororaphis that degrades ethylene precursor ACC, By introducing one or more of a tomato-derived polygalacturonase gene double-stranded RNA that degrades cell wall pectin or a tomato-derived ACC oxidase gene involved in ethylene production. Include tomatoes was improved shelf-life "FLAVR SAVR (trademark)" by introducing a gene pg to generate a double-stranded RNA of the polygalacturonase gene from tomato; tomato shelf-life is improved. Other plants whose maturation characteristics have been modified by gene recombination techniques include, for example, tomatoes, melons, raspberries, strawberries, muskmelons, peppers and papayas whose ripening has been delayed (for example, US 5767376, US7084321, US61075548). , US5981831, WO1995 / 035387, US5952546, US5512466, WO1997 / 001952, WO1992 / 008798 and Plant Cell. 1989, 53-63 (see Plant Molecular Biology, 50, 2002). Methods for producing such plants are generally known to those skilled in the art and are described, for example, in the above-mentioned publications. Preferably, the plants are fruits (eg tomatoes, vines, melons, papayas, bananas, peppers, raspberries and strawberries); nuclear fruits (eg cherries, apricots and peaches); berries (eg apples and berries) Pears); and citrus fruits (eg, citron, lime, orange, pomelo, grapefruit, and mandarin), more preferably selected from tomatoes, melons, papayas, vines, apples, bananas, oranges and strawberries, Most preferred are tomato, melon and papaya.

  Plants to which other quality alterations have been imparted by genetic recombination technology include, for example, endogenous introduction of a 3-phytase gene (phyA) derived from Aspergillus niger, which is a plant phytic acid degrading enzyme. Canola with enhanced degradation of phytic acid “Physased® Canola”; dihydrodoflavonol-4-reductase gene from Petunia hybrida, an enzyme that produces the blue pigment delphinidin and its derivatives, and petunia, Blue flower color by introducing flavonoid-3 ′, 5′-hydroxylase gene derived from pansy (Viola wittrociana), salvia (Salvia splendens), or carnation Controlled carnations “Mondust ™”, “Monoshadow ™”, “Monoshade ™”, “Moonlite ™”, “Moonaqua ™”, “Moonista ™”, “Mooneque” ) "," Moonepearl (TM) "," Moonberry (TM) "and" Moonvelvet (TM) "; anthocyanin-5-acyl from Torenia sp., An enzyme that produces the blue pigment delphinidin and its derivatives A rose whose flower color is controlled to be blue by introducing a transferase gene and a flavonoid-3,5′-hydroxylase gene derived from pansy; a modified cedar pollen antigen protein gene (7crp) is introduced Rice with immunotolerance and alleviation of hay fever; Maize with enhanced degradation of endogenous phytic acid by introducing 3-phytase gene (phyA) from black mold; fiber micronaire, increased fiber strength, long Cotton that produces high-quality fibers with improved uniformity and color (see, for example, WO 1996/26639, US 7329802, US 6472588 and WO 2001/17333).

  Examples of plants whose traits relating to plant growth and yield have been modified include plants with enhanced growth ability. Plants whose growth and yield traits have been modified by genetic recombination techniques are enhanced by introducing a gene (bbx32) that encodes a transcription factor that regulates diurnal properties derived from Arabidopsis thaliana. Soybean, which can be expected to yield high yields; introduction of a transcription factor gene (athb17) belonging to class II HD-Zip II of the homeodomain-leucine 14 zipper (HD-Zip) family derived from Arabidopsis thaliana; As a result, corn with high yields has been developed.

  As a plant whose quality has been modified by genome editing technology, the zinc finger nuclease is used to lack the IPK1 gene encoding inositol-1,3,4,5,6-pentakisphosphate 2-kinase, an enzyme for phytic acid biosynthesis. Corn with reduced phytic acid content due to the loss of phytic acid, browning resistance is conferred by deleting the gene encoding polyphenol oxidase using crisper cassine Mushrooms (see, for example, Nature., Vol 532, 21 APRIL 2016).

  As a plant whose quality has been modified by the new breeding technology, for example, using cisgenesis, introducing a low polyphenol oxidase (enzyme causing browning) production gene sequence GEN-03 isolated from apple into a new apple variety An apple "Arctic (registered trademark)" whose expression level of polyphenol oxidase is reduced and does not turn brown; as an example of giving sapling the properties of GM rootstock, which is a variety improvement technology using grafted trees, a tomato base having salt tolerance The tomato (refer to Physiol Plantarum, 124, 465-475 2005) which gave salt tolerance to the tomato of non-transgenic panicle using a tree is mentioned.

  In rice, genes showing resistance to a large number of diseases, pests and abiotic stress are known, and the production of resistant varieties into which these genes have been introduced is thriving. Examples of genes showing disease resistance in rice and resistance to abiotic stress include BPH1, BPH2, BPH3, BPH4, BPH5, BPH6, BPH7, BPH8, BPH9, BPH10, BPH11, BPH12, BPH13, BPH14, BPH15, BPH17 , BPH18, BPH19, BPH20, BPH21, BPH22, BPH23, BPH24, BPH25, BPH26, BPH27, BPH28, BPH29, BPH32, qBPH-12, qBPHR-1, qBPHR-3, qBPHR-8, qBPHR-5- 1qBPHR-5 -2 qBPHR-11-1, qBPHR-11-2 and other brown planthopper resistance genes; WBPH1, WBPH2, WBPH3, WBPH4, WBPH5, WBPH6, OVC, q Sedron plant resistance genes such as VA-5-2, qOVA1-3, qOVA5-1; Qsbph2b, Qsbph3, Qsbph3b, Qsbph3c, Qsbph3d, Qsbph4, Qsbph8, Qsbph11b, Qsbph11b, Gene; GLH, GLH1, GLH3, GLH4, GLH5, GLH6, GLH7, GLH8, GLH9, GLH10, GLH11, GLH12, GLH13, GRH1, GRH2, GRH3, GRH4, GRH1, HRH, Zlh1 2, leafhopper resistance genes such as qGRH-5, qGRH-6, qGRH-11, and qGRH-3; Antigenic genes; Pii, PI65, PIZT, PI24, PI29, PI25, Pi-jnw1, PB1, PIQ6, PID3, PI67, PITQ5, PITP, PITQ6, PLM2, PISE3, IPI, PISE1, PI157, PIQ4, PI21, PIA, PIB, PIK, PIKUR1, PIKUR2, PI3, PIF, PIZH, PIR4, PIR7, PI30, PI, PIGD2, PIG, PIGD3, PIGD1, PIZ, PI (, PI18, PIM, PI17, PI20, PI1, PI19, PI5, PISH , PI10, PI9, PI21, PI22, PI44, PI22, PI13, PII, PIB1, PIQ1, PIQ2, PIQ3, PIIS1, PII2, PI62, PI12, IPI3, PI14, PI15 , PI16, PIT, PI11, PI6, PI23, PI14, PI11, PIIS2, PIB2, PI12, PI39, PI40, PITA, PIR2-3, PIR9-2, PIR12-2, PIRF2-1, qRBR-2, qRBR-3 , PI27, PI28, PI26, PIGM, PI47, PI48, PI7, PI56, PI49, PI34, PIKG, PI38, PI32, PI31, PI46, PIX, PIXY, Pita3, PI41, PI42, PI2, PI36, PI37, PIKH, PIKM , PIKP, PI35, PIZ5, PIB2, PI43, PI50, PI51, PID1, PIY1, PIY2, PI55-2, PICO39, PI55-1, PIBH8, PIR7A, PIR7B, PID2, PI33, qB R4-1, qBFR4-2, qRBR-2, qRBR-3, qRBR-8, qRBR-1-1, qRBR-1-3, qRBR-7-1, qRBR-7-2, qRBR-9-1, Blast resistance genes such as qRBR-9-2, qRBR-9-3, qRBR-1-2, qRBR-1-4; stripe leaf resistance genes such as STVA, STVB, Stvb-i; XA21D, XA, XA40, XA NM, XA8, XA33, XA34, XA35, XA36, XA37, XA7, XA3, XA25, XA28, XA29, XA30, XA31, XA32, XA38, XA39, XA11, XA16, XA17, XA18, XA19, XA18, XA19 , XA14, XA2, XA12, XA1, XAK, XA A, XA H, XA10, XA23, XA22, XA 24, white leaf blight resistance genes such as XA21, SERRT13, XA4, XA5, and XA13; blight resistance genes such as qSB-2, qSB-3, qSB-7, qSB-11, and qSB-9-1; Sesame leaf blight resistance gene such as CE; yellow dwarf disease resistance gene such as YDV; black stripe dwarf disease resistance gene such as BSV; high temperature cram school resistance gene such as Amy1A, Amy1C, Amy3A, Amy3B; dul3, qAC9 .3, low amylose genes such as rsr1, Wx and Wx1-1; lodging resistance genes such as AP01, SCM2 and Sd1; ear germination resistance genes such as Sdr4; cold tolerance genes such as CTB1, CTB2 and qLTG3-1; Drought tolerance genes such as Dro1; DEP1, Cn1a, GPS, SPIKE, PTB1, TAWAWA1, WFP, IPA1, G 3, GS5, GS6, GL3.1, GW2, GW8, qGL3, qSS7, qSW5 and other genes related to the number of seeds or seeds; Hd1, Ghd8, DTH8 and other genes regulating day length reactivity; FLO4, PDIL1, etc. An endosperm powdery gene; a lipoxygenase-deficient gene (reducing old rice odor) such as LOX3; and a gene related to amylopectin chain length such as Alk are known. Rice varieties in which one or more of these genes are simultaneously incorporated have been developed or marketed.

  For the above-mentioned plants, genetic recombination technology, conventional breeding technology, genome breeding technology, new breeding technology or genome editing technology are used, and abiotic stress resistance, disease resistance, weeding as described above. By crossing two or more plants with similar or different properties, such as drug resistance, pest resistance, growth and yield traits, modification of nutrient utilization, product quality modification, fertility traits, etc. Plants to which two or more properties of the parent line are added are also included.

Commercial plants that have been rendered tolerant to two or more herbicides include, for example, cotton “GlyTol ™ LibertyLink ™” and “GlyTol ™ LibertyLink ™” that are resistant to glyphosate and glufosinate; Corn “Roundup Ready ™ LibertyLink ™ Maize” with glyphosate and glufosinate tolerance; soybean with glufosinate and 2,4-D tolerance “Enlist ™ Soybean”; soybean with glyphosate and dicamba tolerance Genuity® Roundup Ready ™ 2 Xtend ™ ”; Corn and Soybean“ Opti ”with glyphosate and ALS inhibitor tolerance umGAT ™ ”; transgenic soybeans that are resistant to three herbicides, glyphosate, glufosinate and 2,4-D,“ Enlist E3 ™ ”and“ Enlist ™ Roundup Ready 2 Yield ” Maize “Enlist ™ Roundup Ready® Corn 2” resistant to glyphosate, 2,4-D and allyloxyphenoxypropionic acid-based (FOPs) herbicides; glyphosate, 2,4-D and allyloxy Corn “Enlist ™ Roundup Ready® Corn 2” resistant to phenoxypropionic acid (FOPs) herbicides; Cotton “Bollgard II” resistant to dicamba, glyphosate and glufosinate Trademark: XtendFlex (TM) Cotton ";cotton" Enlist (TM) Cotton "resistant to three herbicides, glyphosate, glufosinate and 2,4-D; glyphosate, glufosinate and HPPD herbicides (eg, isoxaflutol Soybean "Liberty Link (registered trademark) GT27 (trademark)" which is resistant to three herbicides. In addition, cotton resistant to both glufosinate and 2,4-D; cotton resistant to both glufosinate and dicamba; corn resistant to both glyphosate and 2,4-D; glyphosate and HPPD herbicide Soybeans resistant to both; glyphosate, glufosinate, 2,4-D, corn resistant to allyloxyphenoxypropionic acid (FOPs) and cyclohexadione (DIMs) herbicides have also been developed.
Examples of commercially available plants imparted with herbicide resistance and pest resistance include corn “YieldGard Roundup Ready ™” and “YieldGard Roundup Ready 2 ™” having glyphosate resistance and resistance to corn borers. Maize “Grurisure CB / LL ™” with glufosinate resistance and corn borer resistance; maize “Yield Gard VT Root worm / RR2 ™” with glyphosate resistance and corn rootworm resistance; Corn “Yield Gard VT Triple ™” with resistance to corn rootworm and corn borer; glufosinate and lepidopteran pest resistance (Cr y1F) (for example, resistance to western bean cut worms, corn borers, black cut worms and fall army worms); “corns having a resistance to glyphosate and corn root worms” YieldGard Corn with corn rootworm / roundup ready 2 ™; glufosinate resistance and corn crustacean pest resistance (Cry3A) (eg resistance to western corn rootworm, northern corn rootworm and mexican corn rootworm) Agurisure GT / RW ™ "; glufosinate and Coleoptera pest resistance (Cry34 / 35Ab1) (eg Western corn root Corn having resistance to glyphosate and corn rootworm resistance “Yield Gard VT Root Worm / RR2®” ) "; Cotton“ Bollgard® 3 XtendFlex (with resistance to ball worms and tobacco badworms, army worms, etc.) resistant to dicamba, glyphosate, glyphosate and cotton lepidoptera Registered trademark) ".

  Examples of commercially available plants imparted with disease resistance and pest resistance include, for example, a potato "Hi-Lite NewLeaf (trademark) Y imparted with potato virus Y resistance and pest resistance. "Potato", "NewLeaf (TM) Y Rushset Burbank Potato" and "Shepody NewLeaf (TM) Y Potato"; Potato leafroll virus (L) and pest resistance (L) "Russet Burbank Potato".

  Commercial plants that have been given herbicide tolerance and quality-modifying properties include, for example, canola “InVigor ™ Canola” that has been given glufosinate tolerance and fertility traits; glufosinate tolerance and fertility traits Corn “InVigor ™ Maize”; soy bean “Visible Gold ™” with glyphosate tolerance and modified oil content.

Examples of commercial plants with more than two traits include glyphosate resistance, glufosinate resistance and lepidopterous insect resistance (Cry1F) (ie against Western bean cut worms, corn borers, black cut worms and fall army worms) Corn “Herculex I / Roundup Ready 2 ™” with resistance); Corn “YieldGard Plus / Roundup Ready 2 ™” with glyphosate resistance, cornroot worm resistance and corn borer resistance; glyphosate tolerance, glufosinate Corn “Agriure GT / CB / LL ™” with tolerance and corn borer resistance; glufosinate resistance, lepidopteran pest resistance (Cry1F) and Lepidoptera pest resistance (Cry34 / 35Ab1) (ie Western bean cut worms, corn borers, black cut worms and fall army worms, etc.) and western corn root worms, northern corn root worms, Mexican corn root worms, etc. Corn “Herculex Xtra ™” with resistance to Coleoptera: glufosinate resistance, corn borer resistance (Cry1Ab) and Coleoptera pest resistance (Cry3A) (ie Western corn rootworm, Northern corn rootworm and Mexican) Corn "Agriure CB / LL / RW (TM)" with resistance to corn rootworms; glyphosate resistance, corn borer resistance (Cry1Ab And "Cori3A", a corn "Agrisure ™ 3000GT" with resistance to Coleoptera and Coleoptera (Cry3A) (ie resistance to Western corn rootworm and Mexican corn rootworm); glyphosate resistance, corn rootworm and European corn borer Maize "Mavera high-value corn" with resistance to lysine and high lysine traits; European corn borers, Southwestern corn borers, corn ear worms, fall army worms, black cut worms and / or western bean worms Corn "Optimum (registered trademark) Leptra (trademark)" that is resistant to insect pests Sex, glufosinate resistance, resistance to soybean leaf spot, sudden death syndrome resistance, resistance to stem stem disease, resistance to phytophathoropathy Sweet root-knot nematode resistance, stem rot resistance, brown stem rot resistance, soybean cyst nematode resistance, iron chloro nematode resistance chloro deficiency, iron chlorosis resistance Soybean “C” with improved iron chlorosis and altered chloride sensitivity edenza (registered trademark) soybean ";cotton" Stoneville (registered trademark) Cotton "provided with a plurality of herbicide resistance and pest resistance (in order to respond to the occurrence of weeds and pests in the field in each region, And ST5517GLTP, ST4848GLT, ST4949GLT, ST5020GLT, ST5115GLT, ST6182GLT, ST4747GLB2, ST4946GLB2, and ST6448GLB2).

  Rice is particularly mentioned as a crop cultivated in the paddy field where the composition of the present invention is used. The rice here refers to Oryza sativa and Oryza glaberrima which are cultivated species among annual plants of the genus Oryza.

  The method of the present invention includes a step of spraying the composition of the present invention, or a herbicidal composition containing fluropyroxifenebenzyl, a herbicidal composition containing one or more compounds selected from the compound group A, and A step of simultaneously spraying a herbicidal composition containing one or more compounds selected from compound group B; The composition of the present invention, or a herbicidal composition containing fluropyroxifene benzyl, a herbicidal composition containing one or more compounds selected from the compound group A, and one or more selected from the compound group B The herbicidal composition containing the compound is treated where weeds or weeds are expected to emerge. Examples of the treatment for the weeds include a treatment for the weeds themselves and a treatment for the soil after the weeds have emerged. Examples of the treatment to a place where weeds are expected to emerge include treatment to the soil surface before weeds emerge.

Examples of the processing method in the method of the present invention include the following modes.
Spraying the soil surface before sowing or transplanting of the crop and before weed emergence;
Spraying the soil surface before sowing or transplanting of the crop and after weed emergence;
Spraying the weeds before sowing or transplanting of the crop and after weed emergence;
Spraying the soil surface after sowing of the crop, before the emergence of the crop and before the emergence of the weeds;
Spraying the soil surface after sowing of the crop, before the emergence of the crop and after the emergence of the weeds;
Spraying the weeds after sowing of the crops, before the emergence of the crops and after the emergence of the weeds;
Spraying the soil surface before weeds emerge in the presence of crops;
A method of spraying on the soil surface after weeds emerged in the presence of crops; and / or a method of spraying on weeds after emergence of weeds in the presence of crops.

  In the method of the present invention, the composition of the present invention, or a herbicidal composition containing fluropyroxifene benzyl, a herbicidal composition containing one or more compounds selected from the compound group A, and the compound group B The herbicidal composition containing one or more selected compounds is sprayed as it is, or is diluted appropriately with water or the like (for example, 100 to 100,000 times) and sprayed using a sprayer. Can do.

  In the method of the present invention, the composition of the present invention, or a herbicidal composition containing fluropyroxifene benzyl, a herbicidal composition containing one or more compounds selected from the compound group A, and the compound group B The herbicidal composition containing one or more selected compounds can be mixed with soil or solid fertilizer and used on the soil surface or water surface at a rate of 100 to 1000 kg per hectare.

  When the method of the present invention is applied to paddy fields, it is usually applied after direct sowing of paddy rice, after direct sowing of dry paddy or after transplanting of paddy rice. The composition of the present invention, or a herbicidal composition containing fluropyroxifene benzyl, a herbicidal composition containing one or more compounds selected from the compound group A, and one or more selected from the compound group B The timing of applying the herbicidal composition containing the compound is immediately after sowing or transplanting of paddy rice to 21 days after sowing or transplanting of paddy rice.

Examples of the weeds that can be controlled by the method of the present invention include the following.
Barnyardgrass (Echinochloa crus-galli), barnyardgrass (Echinochloa oryzicola), barnyardgrass (Echinochloa crus-galli var formosensis), junglerice (Echinochloa colona), Taiwan barnyardgrass (Echinochloa glabrescens), Bruno Gay barnyardgrass (Echinochloa oryzoides), leptochloa chinensis (Leptochloa chinenisis ), Prickly pear millet (Panicum dichotomiflorum), Thai one Iashi (Ischaemum rugosum), Cyperus difformis, Cyperus iria (Cyperus iria), chickweed (C) yperus flaccidus), sedge (Cyperus microiria), Cyperus (Cyperus serotinus), Cyperus (Cyperus rotundus), yellow nutsedge (Cyperus esculentus), Scirpus (Schoenoplectus juncoides), Taiwan Yamai (Schoenoplectus wallichii), Himekan Whangarei (Schoenoplectus mucronatus), pulp ( Schoenoplectus nipponicus, Bolboschoenus koshevikikovii, Kyllinga gracilima, Krogwai kuroguwai Eleocharis acicularis (Eleocharis acicularis), fimbristylis miliacea (Fimbristylis miliacea), Amatsuki (Fimbristylis dichotoma), Monochoria (Monochoria vaginalis), Monochoria korsakowii (Monochoria korsakowii), the United States vaginalis (Heteranthera limosa), false pimpernel (Lindernia pocumbens), Amerikaazena (Lindernia dubia subsp. Major ), Taketozena (Lindernia dubbia subsp. Dubia), Ucozena (Bakopa rotundifolia), Abnomome (Dopatrium junceum), Greater Abalone (Gratiola japonica) , Rotala indica (Rotala indica), Ammannia multiflora Roxb (Ammannia multiflora), e buckwheat Hime Misohagi (Ammannia coccinea), tropical Hime Misohagi (Ammannia auriculata), Elatine triandra Schk (Elatine triandra), arrowhead (Sagittaria pygmaea), Alismataceae (Sagittaria trifolia), Thailand phosphorus Alismataceae ( Sagitaria montevidensis, Limnocharis flava, Heramodala (Alisma canaliculatum), Azio modago-quatica, Hiramsimo (got) Li (Oenanthe javanica), Aeschynomene indica (Aeschynomene indica), the United States horn Aeschynomene indica (Sesbania exaltata), Choujitade (Ludwigia prostrata), ludwigia octovalvis (Ludwigia octovalvis), Bidens Tripartita (Bidens tripartita), Bidens frondosa (Bidens frondosa), Eclipta prostrata (Eclipta thermalis), American Takasaburo (Eclipta alba), Naganoberushi (Sphenochlea zeylanica), Densiou (Marsilea quadrifolia), Japanese morning glory (Ipomoea launcuna), Hosiaeagao (Ipomoe apomoe) ), American morning glory (Ipomoea hederacea), Ipomoea purpurea (Ipomoea purpurea), Liquidambar formosana phosphorus morning glory (Ipomoea wrightii).

  EXAMPLES Hereinafter, although an Example demonstrates this invention, this invention is not limited to these Examples. Further, “g / ha” described in Table 1 indicates the weight grams of the active ingredient per hectare.

Example 1
1/2000 Earl Wagner pot is filled with paddy field soil, water is poured into it, and water is drained. Seeded and cultivated in a greenhouse.
Immediately after sowing, 7 days after sowing, 14 days after sowing, or 21 days after sowing, any one of the combinations of compounds Nos. 1 to 474 shown in Table 1 is put in a pot where rice and weeds are cultivated. Scattering treatment is performed so that the treatment amount of each compound becomes the dose shown in Table 1.
The herbicide spray solution is prepared by dissolving a predetermined amount of each compound in acetone containing 2% (w / v) of Tween 20, and the resulting acetone solution of each compound is adjusted so that the acetone concentration becomes 10% by volume. Prepare by diluting with water and then mixing the resulting water dilutions of each compound. With the water drained, the herbicide spray solution is sprayed from the top surface of the pot at a spray water amount of 100 to 1000 L / ha, and the pot is submerged to 3 to 5 cm one day after spraying.
As a result, all the combinations of Nos. 1 to 474 shown in Table 1 show a high herbicidal effect (synergistic effect) on weeds without causing practically harmful damage to rice.

Table 1

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Example 2
1/2000 Earl Wagner pot is filled with paddy field soil, water is poured into the pot, water is drained, and water is taken out from the pot. And 2-4 leaves of rice are transplanted at a flooding depth of 2-3 cm. In addition, in another pot prepared in the same manner, tubers of Urikawa, Omodaka, Hirumiro, Mitsugayatsuri, Koukiyara, Krogwai and Shizui are planted, and 2-4 leaves of rice are transplanted at a depth of 2-3 cm. Place each pot in a greenhouse to grow weeds and rice.
Among the combinations of compounds numbered 1 to 474 shown in Table 1, any one combination is treated in a pot where rice and weeds are cultivated so that the treatment amount of each compound becomes the dose shown in Table 1. .
The herbicide spray solution is prepared by dissolving a predetermined amount of each compound in acetone containing 2% (w / v) of Tween 20, and the resulting acetone solution of each compound is adjusted so that the acetone concentration becomes 10% by volume. Prepare by diluting with water and then mixing the resulting water dilutions of each compound. The pot is submerged to 3 to 5 cm, and the herbicide spray solution is dropped onto the water surface.
As a result, all the combinations of Nos. 1 to 474 shown in Table 1 show a high herbicidal effect (synergistic effect) on weeds without causing practically harmful damage to rice.

  The present invention can be used to effectively control weeds in the cultivation of paddy rice.

Claims (2)

A herbicidal composition comprising fluropyroxifene benzyl and one or more compounds selected from compound group A consisting of imazosulfuron, propyrisulfuron, and bromobutide. A method of controlling weeds, the step of spraying a herbicidal composition containing fluropyroxifene benzyl and one or more compounds selected from compound group A consisting of propyrisulfuron, imazosulfuron, and bromobutide, or A method comprising a step of simultaneously spraying a herbicidal composition containing fluropyroxifenebenzyl and a herbicidal composition containing one or more compounds selected from the compound group A.