US3385692A - Method for controlling the growth of weeds - Google Patents

Method for controlling the growth of weeds Download PDF

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US3385692A
US3385692A US392305A US39230564A US3385692A US 3385692 A US3385692 A US 3385692A US 392305 A US392305 A US 392305A US 39230564 A US39230564 A US 39230564A US 3385692 A US3385692 A US 3385692A
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ratio
mixed
methylurea
methyluracil
weeds
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US392305A
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Richard N Knowles
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EIDP Inc
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EI Du Pont de Nemours and Co
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Priority to US392305A priority Critical patent/US3385692A/en
Priority to CH1162165A priority patent/CH452992A/en
Priority to FR29397A priority patent/FR1445276A/en
Priority to NL6511107A priority patent/NL6511107A/xx
Priority to BE668792D priority patent/BE668792A/xx
Priority to GB36756/65A priority patent/GB1085516A/en
Priority to DE1567032A priority patent/DE1567032C3/en
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C273/00—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C273/18—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas
    • C07C273/1809—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas with formation of the N-C(O)-N moiety
    • C07C273/1818—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas with formation of the N-C(O)-N moiety from -N=C=O and XNR'R"
    • C07C273/1827—X being H

Definitions

  • This invention relates to methods of destroying weeds with substituted phenylurea compounds. More particularly, this invention refers to a method of controlling the growth of weeds by applying to an area of weed growth 3-(o-fiuorophenyl)-1-rnethylurea.
  • Tri-substituted urea compounds are Well known for their herbicidal properties; see US. Patents 2,655,445 and 2,655,446.
  • Well-known commercial herbicides included within the scope of these patents include monuron, 3-(pchlorophenyl)-1,l-dirnethylurea; and diuron, 3-(3,4-dichlorophenyl)-1,1-dimethylurea.
  • the compound in my invention has a desirable characteristic that makes it more attractive than known herbicides for certain types of herbicidal usage.
  • 3-(o-fluorophenyl)-1-methylurea is substantially more soluble in water than either of the aforementioned commercial herbicides. Accordingly, it is dissipated much more rapidly in the soil.
  • the compound used in my invention is formulated in conventional herbicidal compositions. Usually the compositions will comprise the 3-(o-fluorophenyl-l-methylurea and one or more surface-active agents.
  • the surface-active agent used in this invention can be a wetting, dispersing or an emulsifying agent which will assist dispersion of the compound.
  • the surface-active agent or surfactant can include such anionic, cationic and non-ionic agents as have heretofore been generally employed in plant control compositions of similar type. Suitable surface-active agents are set out, for example, in Searle US. Patent 2,426,417; Todd US. Patent 2,655,447; Jones US. Patent 2,412,510; or Lenher US. Patent 2,139,276. A detailed list of such agents is set forth in Detergents and Emulsifiers Annual (1964) by John W. McCutcheon, Inc.
  • Suitable surface-active agents for use in compositions of the present invention are: polyethylene glycol fatty esters and fatty alkylol amide condensates, alkylaryl sulfonates, fatty alcohol sulfates, dialkyl esters of sodium sulfosuccinate, fatty acid esters of sodium isethionate, polyoxyethylene ethers and thioethers, and long chain quaternary ammonium chloride compounds.
  • Surface-active dispersing agents such as sodium, magnesium or calcium lignin sulfonates, low viscosity methyl cellulose, polymerized sodium salts of alkylnaphthalene sulfonic acids are also suitable in the herbicidal compositions of this invention.
  • the anionic and non-ionic type are the anionic and non-ionic type.
  • the anionic surface-active agents preferred ones are alkali metal or amine salts of alkylbenzene sulfonic acids, such as dodecylbenzenesulfonic acid, sodium lauryl sulfate, alkylnaphthalene sulfonates, sodium N-methyl-N-oleoyltaurate, oleic acid ester of sodium isethionate, dioctyl sodium sulfosuccinate, sodium dodecyldiphenyloxide disulfonate.
  • alkylbenzene sulfonic acids such as dodecylbenzenesulfonic acid, sodium lauryl sulfate, alkylnaphthalene sulfonates, sodium N-methyl-N-oleoyltaurate, oleic acid ester of sodium isethionate, dioctyl sodium
  • alkylphenoxy poly(ethyleneoxy)ethanols such as nonylphenol adducts with ethylene oxide; trimethylnonyl polyethylene glycol ethers, polyethylene oxide adducts of fatty and rosin acids, long chain alkyl mercaptan adducts with ethylene oxide and polyethylene oxide adducts with sorbitan fatty acid esters.
  • the surfaceactive agent in general, less than 10% by Weight of the surfaceactive agent will be used in compositions of this invention and ordinarily the amount of surface-active agents will range from 1-5 but may even be less than 1% by weight.
  • Additional surface-active agents can be added to the above formulation to increase the ratio of surface-active agentzactive agent up to as high as 5 :1 by weight. Normally the purpose of adding higher amounts of surfactant is to increase the herbicidal effect of the active compound. When used at higher rates it is preferred that the surfactant be present in the range of one fifth to five parts surfactant for each one part of 3-(o-fluorophenyl)-1- methylurea.
  • the herbicidal compositions of this invention can contain in addition to the surfactant, finely divided diluents such as talc, natural clay including attapulgite and kaolinite clay, pyrophyllite, diatomaceous earths, synthetic fine silicas, calcium silicate, carbonates, calcium phosphates, sulfur, lime, such flours as walnut shell, wheat, redwood, soybeans and cottonseed.
  • finely divided diluents such as talc, natural clay including attapulgite and kaolinite clay, pyrophyllite, diatomaceous earths, synthetic fine silicas, calcium silicate, carbonates, calcium phosphates, sulfur, lime, such flours as walnut shell, wheat, redwood, soybeans and cottonseed.
  • the amount of finely divided inert solid diluent can vary widely but will generally range from 10 to 98% by Weight of the herbicidal composition.
  • the particle size can vary considerably but will ordinarily 'be somewhat under 50 microns in the finished formulation.
  • compositions containing the 3-(o-fiuorophenyl)-1- methylurea can preferably be in the form of Wettable powders.
  • these contain one or more surfactants and one or more finely divided inert solid diluent, as described above.
  • Other ingredients, such as corrosion inhibitors, stickers, antifoam agents, pigments and the like can be optionally included.
  • Wettable powders are prepared by blending the ingredients and then grinding the composition in a hammer mill, air attrition mill or similar device.
  • Such wettable powders contain from 10 to of the active ingredient, from 1 to 5% surfactant and the remainder finely divided inert solid diluent together with one or more of the optional additives.
  • the particle size of the composition is preferably below 50 microns.
  • compositions commonly used in the herbicide art such as emulsifiable oil solutions, granules, pellets and aqueous suspension concentrates can also be used with the compound used in this invention.
  • the 3-(o-fluorophenyl)-1-methylurea can also be mixed with other herbicides to form a mixture having extremely broad herbicidal activity.
  • the following compounds are mixed in the proportions set forth below.
  • Phenols dinitro-o-sec-butylphenol and its salts pentachlorophenol and its salts These phenols can be mixed with the 3-(o-fluorophenyl)-1-methylurea used in this invention in the proportions of 1:10 to 20:1, respectively, the preferred ratio being 1:5 to 5:1.
  • Carboxylic acids and derivatives The following carboxylic acids and derivatives can be mixed with the 3-(o-fluorophenyl)-1-methylurea used in this invention in the listed proportions:
  • 2,6-dichlorobenzontrile Mixed in a 1:4 to 4:1 ratio, preferably a 1:3 to 3:1 ratio.
  • trichloroacetic acid and its salts Mixed in a 1:2 to 25:1 ratio, preferably a 1:1 to 8:1 ratio.
  • N,N-di(n-propyl)thiolcarbamic acid ethyl ester N,N4ii(n-propy1)thiolcarbamic acid
  • N-propyl ester N-ethyl-N-(n-butyl)thiolcarbamie acid ethyl ester N-ethyl-N-(n-butyl)thiolcarbamic acid
  • n-propyl ester 4 Mixed in a 1:2 to 24:1 ratio, preferably a 1:1 to 12:1 ratio.
  • 2,3,6-trichlorophenylacetic acid and its salts Mixed in a 1:12 to 8:1 ratio, preferably a 1:4 to 4:1 ratio.
  • inorganic and mixed inorganic-organic salts can be mixed with the 3-(o-fluorophenyl)-1-methylurea used in this invention in the listed proportions.
  • B sodium arsenite Mixed in a 1:5 to 40:1 ratio, preferably a 1:4 to 25 :1 ratio.
  • lead arsenate calcium arsenate Mixed in a 150:1 to 600:1 ratio, preferably a :1 to 400:1 ratio.
  • E. ammonium thiocyanate Mixed in a 1:10 to 20:1 ratio, preferably a 1:5 to 5 :1 ratio.
  • ammonium sulfamate Mixed in a 1:1 to 100:1 ratio, preferably a 1:1 to 50:1 ratio.
  • 3,6-endooxohexahydrophthalic acid Mixed in a 1:3 to 20:1 ratio, preferably a 1:2 to :1 ratio.
  • 2,4-dichloro-4-nitrodiphenyl ether Mixed in a 1:10 to 30:1 ratio, preferably a 1:5 to 20:1 ratio.
  • Substituted uracils 3-(o-fiuorophenyl)-1-methylurea can be mixed with substituted uracils, in the proportions listed below.
  • the compound used in this invention is applied in a herbicidally effective amount directly to the soil as a pre-emergence or a post-emergence treatment or it can be mixed intimately with the soil.
  • One half to two pounds per acre of active ingredient will be applied to agricultural soils in order to remove weeds pre-emergence or early post-emergence.
  • the herbicidally effective amount is four to forty pounds per acre depending upon the type of soil.
  • Example 1 The composition is formulated as follows:
  • Example 2 Percent 3-(o-fluorophenyl)-1-methylurea Alkylnaphthalene sulfonate, Na salt 2 Partially desulfonated sodium lignin sulfonate 2 Synthetic fine silica 8 Kaolin clay 8
  • the above composition is blended and micropulverized, then remilled through an air attrition mill until substantially all particles are below ten microns.
  • the above described formulation is applied pre-emergence by means of a tractor mounted sprayer at the rate of 1.5 pounds of active ingredient per acre to a plot of newly-planted potatoes.
  • the potatoes emerge to a good stand and develop an excellent crop.
  • Weeds such as giant foxtail, barnyard grass, crabgrass, velvet leaf and pigweed germinate normally but within a few days succumb to the action of the chemical.
  • Example 3 Percent 3-(o-fluorophenyl)-1-methylurea 8O Attapulgite clay 18 Dioctyl sodium sulfosuccinate 1 Sodium lignin sulfonate 1 Twenty five pounds of the above formulation is suspended in forty gallons of water and applied at the beginning of the growing season to an industrial type outdoor storage area which is one acre in size. A mixed stand of weedy vegetation including crabgrass, yellow foxtail, goosegrass, wild mustard, black-eyed susan, smartweed and morning glory germinate but die within ten days.
  • Method for controlling the growth of weeds comprising applying to an area of weed growth a herbicidally effective amount of 3-(o-fluorophenyl)-1-methylurea.
  • Method for controlling the growth of weeds growing among cotton plants comprising applying to an area of weed growth within a cotton field a herbicidally effective amount of 3-(o-fluorophenyl)-1-methylurea.
  • Method for controlling the growth of weeds growing among potato plants comprising applying to an area of weed growth within potato field a herbicidally effective amount of 3-(o-fluorophenyl)-1-methylurea.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

United States Patent 3,385,692 METHOD FOR CONTROLLING THE GROWTH OF WEEDS Richard N. Knowles, Hockessin, Del., assignor to E. I. du Pont de Nemours and Company, Wilmington, DeL, a corporation of Delaware No Drawing. Filed Aug. 26, 1964, Ser. No. 392,305 3 Claims. (Cl. 71-120) ABSTRACT OF THE DISCLOSURE Controlling the growth of weeds with 3-(o-fiuorophenyl)-l-methylurea.
This invention relates to methods of destroying weeds with substituted phenylurea compounds. More particularly, this invention refers to a method of controlling the growth of weeds by applying to an area of weed growth 3-(o-fiuorophenyl)-1-rnethylurea.
Tri-substituted urea compounds are Well known for their herbicidal properties; see US. Patents 2,655,445 and 2,655,446. Well-known commercial herbicides included within the scope of these patents include monuron, 3-(pchlorophenyl)-1,l-dirnethylurea; and diuron, 3-(3,4-dichlorophenyl)-1,1-dimethylurea. I have now discovered another outstanding urea herbicide characterized as a disubstituted urea molecule.
The compound in my invention has a desirable characteristic that makes it more attractive than known herbicides for certain types of herbicidal usage. I have found that 3-(o-fluorophenyl)-1-methylurea is substantially more soluble in water than either of the aforementioned commercial herbicides. Accordingly, it is dissipated much more rapidly in the soil.
The compound used in my invention is formulated in conventional herbicidal compositions. Usually the compositions will comprise the 3-(o-fluorophenyl-l-methylurea and one or more surface-active agents.
The surface-active agent used in this invention can be a wetting, dispersing or an emulsifying agent which will assist dispersion of the compound. The surface-active agent or surfactant can include such anionic, cationic and non-ionic agents as have heretofore been generally employed in plant control compositions of similar type. Suitable surface-active agents are set out, for example, in Searle US. Patent 2,426,417; Todd US. Patent 2,655,447; Jones US. Patent 2,412,510; or Lenher US. Patent 2,139,276. A detailed list of such agents is set forth in Detergents and Emulsifiers Annual (1964) by John W. McCutcheon, Inc.
Suitable surface-active agents for use in compositions of the present invention are: polyethylene glycol fatty esters and fatty alkylol amide condensates, alkylaryl sulfonates, fatty alcohol sulfates, dialkyl esters of sodium sulfosuccinate, fatty acid esters of sodium isethionate, polyoxyethylene ethers and thioethers, and long chain quaternary ammonium chloride compounds.
Surface-active dispersing agents such as sodium, magnesium or calcium lignin sulfonates, low viscosity methyl cellulose, polymerized sodium salts of alkylnaphthalene sulfonic acids are also suitable in the herbicidal compositions of this invention.
Among the more preferred surfactants are the anionic and non-ionic type. Among the anionic surface-active agents, preferred ones are alkali metal or amine salts of alkylbenzene sulfonic acids, such as dodecylbenzenesulfonic acid, sodium lauryl sulfate, alkylnaphthalene sulfonates, sodium N-methyl-N-oleoyltaurate, oleic acid ester of sodium isethionate, dioctyl sodium sulfosuccinate, sodium dodecyldiphenyloxide disulfonate. Among the 3,385,692 Patented May 28, 1968 non-ionic compounds, preferred members are alkylphenoxy poly(ethyleneoxy)ethanols such as nonylphenol adducts with ethylene oxide; trimethylnonyl polyethylene glycol ethers, polyethylene oxide adducts of fatty and rosin acids, long chain alkyl mercaptan adducts with ethylene oxide and polyethylene oxide adducts with sorbitan fatty acid esters.
In general, less than 10% by Weight of the surfaceactive agent will be used in compositions of this invention and ordinarily the amount of surface-active agents will range from 1-5 but may even be less than 1% by weight.
Additional surface-active agents can be added to the above formulation to increase the ratio of surface-active agentzactive agent up to as high as 5 :1 by weight. Normally the purpose of adding higher amounts of surfactant is to increase the herbicidal effect of the active compound. When used at higher rates it is preferred that the surfactant be present in the range of one fifth to five parts surfactant for each one part of 3-(o-fluorophenyl)-1- methylurea.
The herbicidal compositions of this invention can contain in addition to the surfactant, finely divided diluents such as talc, natural clay including attapulgite and kaolinite clay, pyrophyllite, diatomaceous earths, synthetic fine silicas, calcium silicate, carbonates, calcium phosphates, sulfur, lime, such flours as walnut shell, wheat, redwood, soybeans and cottonseed.
The amount of finely divided inert solid diluent can vary widely but will generally range from 10 to 98% by Weight of the herbicidal composition. The particle size can vary considerably but will ordinarily 'be somewhat under 50 microns in the finished formulation.
Compositions containing the 3-(o-fiuorophenyl)-1- methylurea can preferably be in the form of Wettable powders. In addition to the active ingredient these contain one or more surfactants and one or more finely divided inert solid diluent, as described above. Other ingredients, such as corrosion inhibitors, stickers, antifoam agents, pigments and the like can be optionally included.
These Wettable powders are prepared by blending the ingredients and then grinding the composition in a hammer mill, air attrition mill or similar device. Such wettable powders contain from 10 to of the active ingredient, from 1 to 5% surfactant and the remainder finely divided inert solid diluent together with one or more of the optional additives. The particle size of the composition is preferably below 50 microns.
Other compositions commonly used in the herbicide art, such as emulsifiable oil solutions, granules, pellets and aqueous suspension concentrates can also be used with the compound used in this invention.
The 3-(o-fluorophenyl)-1-methylurea can also be mixed with other herbicides to form a mixture having extremely broad herbicidal activity. The following compounds are mixed in the proportions set forth below.
Substituted ureas 3- 3 ,4 dichlorophenyl)-1,1-dimethy1urea 3 -(4-chlorophenyl)-1,1-dimethylurea 3 -phenyl-1,l-dimethylurea '3 3 ,4-dichlorophenyl) 1 -n-butyll-methylurea 3 -(3,4dichlorophenyl) -1-methoXy-1-methylurea 3- (4-chlorophenyl) -1-methoxy-1-methylurea 3- (3 ,4-dichlorophenyl) -1, l ,3 -trimethylurea 3-(p-chlorophenoxyphenyl) -1,1-dimethylurea l- Z-methylcycylohexyl -3 -phenylurea The above ureas can be mixed with the 3-(o-fiuorophenyl) -1-methylurea used in this invention in proportions 3 of from 1:4 to 4: 1, respectively, the preferred ratio being 1:2 to 2: 1.
Substituted triazines 2-chloro-4,6-bis (ethylamino) -s-triazine 2-chloro-4-ethylarnino-6-isopropylamino-s-triazine 2-chloro-4,6-bis(methoxypropylamino) -s-triazine 2-methoxy-4,6-bis (isopropylamino)-s-triazine 2-methylmercapto-4,6-bis (isopropylarnino) -s-triazi ne 2-methylmercapto-4,6-bis(ethylamino)-s-triazine 2-methylmercapto-4-ethylamino-6-isopropylamino-striazine 2-.methoxy-4,6-bis (ethylamino) striazine 2-metl1oxy-4-ethylamino-6-isopropylamino-s-triazine 2-chl0ro-4,6-bis(isopropylamino) -s-triazine These triazines can be mixed with the 3-(o-fiuorophenyl)- l-rnethylurea used in this invention in proportions of from 1:4 to 4:1 respectively, the preferred ratio being 1:2 to 2: 1.
Phenols dinitro-o-sec-butylphenol and its salts pentachlorophenol and its salts These phenols can be mixed with the 3-(o-fluorophenyl)-1-methylurea used in this invention in the proportions of 1:10 to 20:1, respectively, the preferred ratio being 1:5 to 5:1.
Carboxylic acids and derivatives The following carboxylic acids and derivatives can be mixed with the 3-(o-fluorophenyl)-1-methylurea used in this invention in the listed proportions:
Mixed in a 1:16 to 8:1 ratio, preferably a 1:4 to 4:1
ratio.
2,6-dichlorobenzontrile Mixed in a 1:4 to 4:1 ratio, preferably a 1:3 to 3:1 ratio.
trichloroacetic acid and its salts Mixed in a 1:2 to 25:1 ratio, preferably a 1:1 to 8:1 ratio.
2,2-dichloropropionic acid and its salts Mixed in a 1:4 to 8:1 ratio, preferably a 1:2 to 4:1
ratio.
N,N-di(n-propyl)thiolcarbamic acid, ethyl ester N,N4ii(n-propy1)thiolcarbamic acid, N-propyl ester N-ethyl-N-(n-butyl)thiolcarbamie acid, ethyl ester N-ethyl-N-(n-butyl)thiolcarbamic acid, n-propyl ester 4 Mixed in a 1:2 to 24:1 ratio, preferably a 1:1 to 12:1 ratio.
N-phenylcarbamic acid, Z-methylcyclohexyl ester N-phenylcarbamic acid, isopropyl ester N-(m-chlorophenyl)carbamic acid, isopropyl ester N-(m-chlorophenyl)carbamic acid, 4-chloro-2-butynyl ester Mixed in a 1:2 to 24:1 ratio, preferably a 1:1 to 12:1 ratio.
2,3,6-trichlorophenylacetic acid and its salts Mixed in a 1:12 to 8:1 ratio, preferably a 1:4 to 4:1 ratio.
2-chloro-N,N-diallylacetamide maleic hydrazide Mixed in a 1:2 to 10:1 ratio, preferably a 1:1 to 5:1 ratio.
Inorganic and mixed inorganic-organic salts The following salts can be mixed with the 3-(o-fluorophenyl)-1-methylurea used in this invention in the listed proportions.
A. calcium propylarsonate disodium monomethylarsonate octyl-dodecylammoniummethylarsonate dimethylarsinic acid Mixed in a 1:4 to 4:1 ratio, preferably a 1:2 to 2:1 ratio.
B. sodium arsenite Mixed in a 1:5 to 40:1 ratio, preferably a 1:4 to 25 :1 ratio.
lead arsenate calcium arsenate Mixed in a 150:1 to 600:1 ratio, preferably a :1 to 400:1 ratio.
sodium tetraborate hydrated, granulated sodium metaborate sodium pentaborate polyborchlorate unrefined borate or such as borascu Mixed in a 3:1 to 1500:1, preferably a 6:1 to 1000:1 ratio.
E. ammonium thiocyanate Mixed in a 1:10 to 20:1 ratio, preferably a 1:5 to 5 :1 ratio.
F. sodium chlorate Mixed in a 1:1 to 40:1 ratio, preferably a 2:1 to 20:1 ratio.
' G. ammonium sulfamate Mixed in a 1:1 to 100:1 ratio, preferably a 1:1 to 50:1 ratio.
Other organic herbicides These organic herbicides can be mixed with the 3-(0- fluorophenyl)-1-methylurea used in this invention in the listed proportions:
5,6-dihydro-(4A,6A) -dipyrido-(1,2-A,2', '-C) pyrazinium dibromide Mixed in a 1:20 to 16:1 ratio, preferably a 1:5 to 5:1 ratio.
B. 3 -amino-l,2,4-triazole Mixed in a 1:20 to 20:1 ratio, preferably a 1:5 to 5:1 ratio.
3,6-endooxohexahydrophthalic acid Mixed in a 1:3 to 20:1 ratio, preferably a 1:2 to :1 ratio.
D. hexachloroacetone Mixed in a 1:2 to 16:1 ratio, preferably a 1:1 to 8:1 ratio.
' E. diphenylacetonitrile N,N-dimethyl-u,u-diphenylacetamide N,N-di-n-propyl-2,6-dinitro-4-trifiuoromethylaniline N,N-di-n-propyl-2,6-dinitro-4-methylaniline Mixed in a 1:10 to 30:1 ratio, preferably a 1:5 to :1 ratio.
O-(2,4-dichlorophenyl)-O-methyl-isopropylphosphoramidothiate 2,3,5,6-tetrachloroterephthalic acid, dimethyl ester Mixed in a 1:4 to 20:1 ratio, preferably a 1:3 to 51:1 ratio.
2,4-dichloro-4-nitrodiphenyl ether Mixed in a 1:10 to 30:1 ratio, preferably a 1:5 to 20:1 ratio.
Substituted uracils 3-(o-fiuorophenyl)-1-methylurea can be mixed with substituted uracils, in the proportions listed below.
3-cyclohexyl-6-rnethyluracil 3-cyclohexyl-6-ethyluracil 3-cycl0hexyl-6-sec-butyluracil 3-norbornyl-6-methyluracil 3-cyclopentyl-6-methyluracil 3-cycl0hexyl-6-isopropyluracil 5-bromo-3-sec-butyl-6-methyluracil 5-chloro-3-sec-butyl-6-methyluracil 5-bromo-3-tert-butyl-6-methyluracil 5-chloro-3-tert-butyl-6-methyluracil 5-bromo-3 l-ethylpropyl 6-methyluracil 5 -chloro-3-( l-ethylpropyl) -6-methyluracil 5-bromo-3-isopropyl-6-rnethyluracil 5-chloro-3-isopropyl-6-methyluracil 5-chloro-3-cyclohexylmethyl-6-methyluracil 5-methoxy-3-cyclohexyl-6-methyluracil 3-sec-butyl-S,6-dimethyluracil 5-bromo-3-norbornylmethyl-6-methyluracil S-nitro-3-sec-butyl-6-methyluracil 3-cyclohexyl-5 ,6-dimethyluracil 5-bromo-3 -cyclohexyl-6-methyluracil 5-chloro-3-phenyl-6-methyluracil Mixed in a 1:4 to 4:1 ratio, preferably a 1:2 to 2:1 ratio.
3-cyclohexyl-5 ,6-trimethyleneuracil 3-sec-butyl-5 ,6-trimethyleneuracil 3-isopropyl-5,G-trimethyleneuracil 3 -isopropyl-S,6-tetramethyleneuracil 3-isopropyl-5,6-pentamethyleneuracil Mixed in a 1:6 to 6:1 ratio, preferably a 1:4 to 4:1 ratio.
3 -cyclohexyl-5-bromouracil 3 -cyclohexyl-5-chlorouracil 3-isopropyl-5-bromouracil 3-sec-butyl-5-bromouracil 3-sec-butyl-5-chlorouracil Mixed in a 1:6 to 6:1 ratio, preferably a 1:2 to 2:1 ratio.
3-isopropyl-1-trichloromethylthio-S-bromo-6- methyluracil 3-cyclohexyl-1-trichloromethylthio-5-bromo-6- methyluracil 3-sec-butyll-acetyl-5-bromo-6-methyluraci1 3-isopropyl-1-acetyl-5-bromo-6-methyluracil 3-isopropyl-1-trichloromethylthio-5-chloro-6- methyluracil Mixed in a 1:4 to 4:1 ratio, preferably a 1:2 to 2:1 ratio.
All of the foregoing ratios are weight ratios.
The compound used in this invention is applied in a herbicidally effective amount directly to the soil as a pre-emergence or a post-emergence treatment or it can be mixed intimately with the soil. One half to two pounds per acre of active ingredient will be applied to agricultural soils in order to remove weeds pre-emergence or early post-emergence. When soil sterilization is desired the herbicidally effective amount is four to forty pounds per acre depending upon the type of soil.
The following additional examples are set forth to provide a still clearer understanding of the invention.
Example 1 The composition is formulated as follows:
Percent 3-(o-fiuorophenyl)-1-rnethylurea 50 Attapulgite clay 48 Dioctyl sodium sulfosuccinate 1 Sodium lignin sulfonate 1 The above composition is applied at the rate of 1.5 .pounds of active ingredient to a field of cotton which is in the process of being planted. Good pre-emergence control of weeds is obtained for a period of six to eight weeks. The Weeds present are crabgrass, Johnsong-rass seedlings, Florida pursley and annual morning glory. The crop shows normal growth.
Example 2 Percent 3-(o-fluorophenyl)-1-methylurea Alkylnaphthalene sulfonate, Na salt 2 Partially desulfonated sodium lignin sulfonate 2 Synthetic fine silica 8 Kaolin clay 8 The above composition is blended and micropulverized, then remilled through an air attrition mill until substantially all particles are below ten microns.
The above described formulation is applied pre-emergence by means of a tractor mounted sprayer at the rate of 1.5 pounds of active ingredient per acre to a plot of newly-planted potatoes. The potatoes emerge to a good stand and develop an excellent crop. Weeds such as giant foxtail, barnyard grass, crabgrass, velvet leaf and pigweed germinate normally but within a few days succumb to the action of the chemical.
Example 3 Percent 3-(o-fluorophenyl)-1-methylurea 8O Attapulgite clay 18 Dioctyl sodium sulfosuccinate 1 Sodium lignin sulfonate 1 Twenty five pounds of the above formulation is suspended in forty gallons of water and applied at the beginning of the growing season to an industrial type outdoor storage area which is one acre in size. A mixed stand of weedy vegetation including crabgrass, yellow foxtail, goosegrass, wild mustard, black-eyed susan, smartweed and morning glory germinate but die within ten days.
The invention claimed is:
1. Method for controlling the growth of weeds comprising applying to an area of weed growth a herbicidally effective amount of 3-(o-fluorophenyl)-1-methylurea.
2. Method for controlling the growth of weeds growing among cotton plants comprising applying to an area of weed growth within a cotton field a herbicidally effective amount of 3-(o-fluorophenyl)-1-methylurea.
3. Method for controlling the growth of weeds growing among potato plants comprising applying to an area of weed growth within potato field a herbicidally effective amount of 3-(o-fluorophenyl)-1-methylurea.
References Cited UNITED STATES PATENTS 2,625,561 1/1953 Werntz 260-553 2,655,446 10/1953 Todd 71120 3,134,665 5/1964 Martin et a1. 71120 FOREIGN PATENTS 1,034,658 4/ 1953 France.
JAMES O. THOMAS, The, Primary Examiner.
US392305A 1964-08-26 1964-08-26 Method for controlling the growth of weeds Expired - Lifetime US3385692A (en)

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US392305A US3385692A (en) 1964-08-26 1964-08-26 Method for controlling the growth of weeds
CH1162165A CH452992A (en) 1964-08-26 1965-08-18 Herbicides
FR29397A FR1445276A (en) 1964-08-26 1965-08-25 Herbicides
NL6511107A NL6511107A (en) 1964-08-26 1965-08-25
BE668792D BE668792A (en) 1964-08-26 1965-08-25
GB36756/65A GB1085516A (en) 1964-08-26 1965-08-26 Herbicidal compositions
DE1567032A DE1567032C3 (en) 1964-08-26 1965-08-26 Herbicides

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3518304A (en) * 1967-10-17 1970-06-30 Rohm & Haas Fluoroureas
US3960943A (en) * 1974-11-25 1976-06-01 Chevron Research Company N-cycloalkyldithio-N'-fluorophenyl ureas
US3990884A (en) * 1969-10-23 1976-11-09 Fisons Limited Herbicidal Composition Comprising 4-chloro-2-butynyl m-chlorocarbanilate
US4452631A (en) * 1981-07-06 1984-06-05 Eli Lilly And Company Urea herbicides

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4313755A (en) * 1980-07-21 1982-02-02 Shell Oil Company N-Cyclopyopyl-N-(fluorophenyl)-N-acylureas and their herbidical use

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2625561A (en) * 1950-10-27 1953-01-13 Du Pont Fluoroaromatic isocyanates
FR1034658A (en) * 1949-12-06 1953-07-29 Du Pont New herbicidal compositions
US2655446A (en) * 1952-02-14 1953-10-13 Du Pont Chemical compositions and methods
US3134665A (en) * 1959-08-21 1964-05-26 Ciba Ltd Method for destroying weeds

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1034658A (en) * 1949-12-06 1953-07-29 Du Pont New herbicidal compositions
US2625561A (en) * 1950-10-27 1953-01-13 Du Pont Fluoroaromatic isocyanates
US2655446A (en) * 1952-02-14 1953-10-13 Du Pont Chemical compositions and methods
US3134665A (en) * 1959-08-21 1964-05-26 Ciba Ltd Method for destroying weeds

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3518304A (en) * 1967-10-17 1970-06-30 Rohm & Haas Fluoroureas
US3990884A (en) * 1969-10-23 1976-11-09 Fisons Limited Herbicidal Composition Comprising 4-chloro-2-butynyl m-chlorocarbanilate
US3960943A (en) * 1974-11-25 1976-06-01 Chevron Research Company N-cycloalkyldithio-N'-fluorophenyl ureas
US4452631A (en) * 1981-07-06 1984-06-05 Eli Lilly And Company Urea herbicides

Also Published As

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NL6511107A (en) 1966-02-28
CH452992A (en) 1968-03-15
DE1567032B2 (en) 1974-01-03
DE1567032C3 (en) 1974-09-05
GB1085516A (en) 1967-10-04
BE668792A (en) 1965-12-16
DE1567032A1 (en) 1970-06-25

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