USH224H - Glycoside-containing agricultural treatment composition - Google Patents

Glycoside-containing agricultural treatment composition Download PDF

Info

Publication number
USH224H
USH224H US06/739,241 US73924185A USH224H US H224 H USH224 H US H224H US 73924185 A US73924185 A US 73924185A US H224 H USH224 H US H224H
Authority
US
United States
Prior art keywords
composition
glycoside
percent
active ingredient
dispersing agent
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US06/739,241
Inventor
Arshad H. Malik
Arno Cahn
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
AE STALEY MAUFACTURING Co A CORP OF
Henkel Corp
Original Assignee
Tate and Lyle Ingredients Americas LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Tate and Lyle Ingredients Americas LLC filed Critical Tate and Lyle Ingredients Americas LLC
Priority to US06/739,241 priority Critical patent/USH224H/en
Assigned to A.E. STALEY MAUFACTURING COMPANY A CORP OF DE reassignment A.E. STALEY MAUFACTURING COMPANY A CORP OF DE ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: CAHN, ARNO, MALIK, ARSHAD H.
Priority to US06/921,706 priority patent/USH303H/en
Application granted granted Critical
Publication of USH224H publication Critical patent/USH224H/en
Assigned to HENKEL CORPORATION, 300 BROOKSIDE AVE., AMBLER, PA 19002, A DE CORP. reassignment HENKEL CORPORATION, 300 BROOKSIDE AVE., AMBLER, PA 19002, A DE CORP. ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: A.E. STALEY MANUFACTURING COMPANY
Abandoned legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/30Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants

Definitions

  • a dispersing aid which is not itself environmentally harmful either to the products to which it is applied or to the applicator of the composition. It is also desirable that the dispersing aid aspect of the present invention use a material which has emulsifying characteristics as well as being useful in dispersing the product in its application. It is also desirable to replace materials such as Cellosolve solvents typically used in numerous agricultural formulations. The Cellosolve solvents have been speculated to be carcinogenic materials which may also cause sterility. The particular dispersing agents with which the present invention is concerned have considerably less volatility than do the Cellosolve materials and thus may be retained for longer periods on plants or other surfaces on which the composition is applied.
  • Isourea plant growth regulators such as N-methoxycarbonyl-N'-methylphenylcarbamoylethylisourea and 1-(4-chlorophenylcarbamoyl)-3-ethoxycarbonyl-2-methylisourea; another type of plant growth regulators such as sodium naphthaleneacetate, 1,2-dihydropyridazine-3,-6-dione and gibberellins; triazine herbicides such as 2-methylthio-4,6-bisethylamino-1,3,5-triazine, 2-chloro-4,6-bisethylamino-1,3,5-triazine, 2-methoxy-4-ethylamino-6-isopropylamino-1,3,5-triazine, 2-chloro-4-ethylamino-6-isopropylamino-s-triazine, 2-methylthio-4,6-bis(isopropylamin
  • 2-chloro-4-methylphenoxyacetic acid 4-chloro-2-methylphenoxyacetic acid and ethyl 2-methyl-4-chlorophenoxybutylate
  • diphenylether herbicides such as 2,4,6-trichlorophenyl-4'-nitrophenylether,2,4-dichlorophenyl-4'-nitrophenylether and 3,5-dimethylphenyl-4'-nitrophenylether
  • urea herbicides such as 3-(3,4-dichlorophenyl)-1-methoxy-1-methyl urea, 3-(3,4-dichlorophenyl)-1,1-dimethylurea and 3-(4-chlorophenyl)-1,1-dimethyl urea
  • carbamate herbicides such as 3-methoxycarbonylaminophenyl-N-(3-methylphenyl)carbamate, isopropyl-N-(3-chlorophenyl)carbamate and methyl-N-(3,
  • insect repellents may be employed herein: 2-ethyl-1,3-hexanediol; N-octyl bicycloheptene dicarboximide; N,N-diethyl-M-toluamide; 2,3:4,5-Bis (2-butylene) tetrahydro-2-furaldehyde; Di-n-propyl isocinchomeronate; and 2-hydroxyethyl-n-octyl sulfide.
  • compositions of the present invention will contain from about 5 percent to about 95 percent; preferably from about 10 percent to about 95 percent by weight water. Additional solvents may be added by the applicator to dilute out the composition.
  • the products of the present invention may be formulated as aqueous products ready for use if desired. The products may be applied by aerial spraying, by in seed row application or with a fertilizer or the like.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Agronomy & Crop Science (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

This invention describes a composition of matter and a method of treating agricultural substrates in which an active ingredient selected from the group consisting of fungicides, bactericides, insecticides, insect repellents, herbicides and plant growth regulators and mixtures thereof is utilized in conjunction with an amount of a glycoside dispersing agent selected from the group consisting of fructoside, glucoside, mannoside, galactoside, taloside, guloside, alloside, altroside, idoside, arabinoside, xyloside, lyxoside and riboside and mixtures thereof which is sufficient to form an emulsion or dispersion of the active ingredient.

Description

BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention deals with the forming of dispersions or emulsions and dry product application of various biologically active ingredients.
2. Description of the Art
It is known that various materials such as insecticides, insect repellents, fungicides, bactericides, herbicides, and plant growth regulators may formulated into various products for use on crops, for insect control, weed control and the like. Often, these products are applied as a dry powder or a granular material to the surface which is desired to be treated. In still other cases, the products are formulated as a liquid or a semi-solid dispersion. Whether the method of application is dry or wet, it is advantageous to include within the product a dispersing agent to control the flow of the product to ensure equal distribution of the active ingredient throughout the remaining components of the composition.
The typical composition used for herbicide, fungicide, insecticide, bactericide or herbicide ingredients has ordinarily depended on the end-use method of application. That is, a specific dispersing aid is often employed when the product is to be applied in a powder or dry form and yet a second different dispersing aid is required when the product is to be applied as a semi-solid or liquid composition. It would be advantageous to prepare a product comprising the active ingredient and to utilize a single dispersing agent without regard to whether the final use application of the product is in a liquid or solid formulation. Moreover, the desirability of using a single ingredient as a dispersing agent reduces the possibility for error given the number of chemicals which must be compounded to prepare a herbicide or insecticide product.
It is also highly desirable to incorporate into the compositions with which the present invention deals, a dispersing aid which is not itself environmentally harmful either to the products to which it is applied or to the applicator of the composition. It is also desirable that the dispersing aid aspect of the present invention use a material which has emulsifying characteristics as well as being useful in dispersing the product in its application. It is also desirable to replace materials such as Cellosolve solvents typically used in numerous agricultural formulations. The Cellosolve solvents have been speculated to be carcinogenic materials which may also cause sterility. The particular dispersing agents with which the present invention is concerned have considerably less volatility than do the Cellosolve materials and thus may be retained for longer periods on plants or other surfaces on which the composition is applied. The emulsifying and dispersing capabilities of the dispersing agents of the present invention also make them less resistant to being removed by rain from the surface of a growing plant. The reader is suggested to review U.S. Pat. No. 4,512,989 issued Apr. 23, 1985 to Ohyama et al. for a general disclosure of agricultural compositions with which the present invention is concerned.
Throughout the specification and claims, percentages and ratios are by weight; temperatures are in degrees Celsius and pressures are in KPascals unless otherwise indicated. To the extent applicable, references to patents and articles are herein incorporated by reference.
SUMMARY OF THE INVENTION
This invention describes composition of matter comprising an active ingredient consisting of fungicides; bactericides; insecticides; insect repellents; herbicides and plant growth regulators and mixtures thereof and an effective amount of a glycoside dispersing agent selected from the group consisting of fructoside, glucoside, mannoside, galactoside, taloside, guloside, alloside, altroside, idoside, arabinoside, xyloside, lyxoside and riboside and mixtures thereof in a sufficient amount to form an emulsion or dispersion of the active ingredient.
A further aspect of the invention is a method of treatment an agricultural substrate comprising introducing to the substrate a sufficient amount to accomplish the treatment of a composition of matter comprising an active ingredient consisting of fungicides; bactericides; insecticides; herbicides and plant growth regulators and mixtures thereof and an effective amount of a glycoside dispersing agent selected from the group consisting of fructoside, glucoside, mannoside, galactoside, taloside, guloside, alloside, altroside, idoside, arabinoside, xyloside, lyxoside and riboside and mixtures thereof in a sufficient amount to form an emulsion or dispersion of the active ingredient.
DETAILED DESCRIPTION OF THE INVENTION
Glycosides useful in the present invention include those prepared according to U.S. Pat. No. 3,219,656 to Boettner issued Nov. 23, 1965. Further glycosides which may be used herein include the alkyl polyglycosides described in U.S. Pat. No. 3,598,865 issued Aug. 10, 1971 to Lew. Useful saccharide moieties for the glycoside include fructosides, glucosides, mannosides, galactosides, talosides, gulosides, allosides, altrosides, idosides, arabinosides, xylosides, lyxosides and ribosides and mixtures thereof. The preferred sacchride moieties are glucosides, fructosides and xylosides.
The structural formula R(OG)x as defined herein preferably has the hydrophobic moiety (aglycone portion) of the glycoside containing between about 1 and 30 carbon atoms; preferably from about 1 to about 20 carbon atoms; and most preferably from about 9 to about 18 carbon atoms. In formulations where it is desired to prepare the product as a powdered or polverant material the aglycone portion preferably contains from about 1 to about 8 carbon atoms and in particular is a 2-ethylhexyl radical or other branched material.
The value O is an oxygen atom in the structural formula while the value x is referred to as the degree of polymerization or DP indicating the number of sacchraide units in the glycosyl portion of the molecule. Typically, the degree of polymerization on average will be between 1 and about 18; preferably from about 1 to about 15; and most preferably from about 1.2 to about 4. Where a powdered or polverant product is preferred it is often desired to utilize the material where the DP is substantially 1. The saccharide backbone (glycosyl) as defined herein is the portion (G) of the molecule.
Where desired in the present invention the glycosides may contain an alkylene oxide unit such as propylene oxide or ethylene oxide between the hydrophobic moiety (aglycone portion) of the glycoside molecule and the saccharide backbone.
Where it is also desirable, the glycoside may contain pendant alkylene oxide units such as ethylene propylene oxide. A disclosure of the manufacture of such glycosides is found in Ser. No. 06/704,828 filed Feb. 25, 1985 by Roth et al. and herein incorporated by reference. As noted previously, the scope of the present invention is particularly broad based in that glycoside materials over a wide range of values according to the structural formula R(OG)x are useful. It is believed that the lower DP, lower alkyl chain-length materials tend to be rather water insoluble and thus excellent for incorporation in powdered or polverant products whereas the higher DP materials are valuable in that they have substantial emulsification capacity to function as a dispersing agent in the present invention. Generally, as the number of carbon atoms in the aglycone portion of the molecule increases the product becomes less water-soluble, thereby holding the active ingredient on the plant surface.
The active ingredients in the present invention are as follows:
FUNGICIDES AND BACTERICIDES
Carbamate fungicides such as 3,3'-ethylenebis (tetrahydro-4,6-dimethyl-2H-1,3,5-thiadiazine-2-thione), zinc or manganese ethylenebis(dithicarbamate), bis(dimethyldithiocarbamoyl)disulfide, zinc propylenebis (dithiocarbamate), bis(dimethyldithiocarbamoyl) ethylenediamine; nickel dimethyldithiocarbamate, methyl-1(butylcarbamoyl)-2-benzimidazolecarbamate, 1,2-bis(3-methoxycarbonyl-2-thioureido)benzene, 1-isopropylcarbamoyl-3-(3,5-dichlorophenyl)hydration, potassium N-hydroxymethyl-N-methyldithiocarbamate and 5-methyl-10-butoxycarbonylamino-10, 11-dehydrodibenzo (b,f)azepine; pyridine fungicides such as zinc bis(2-hydroxy-2-(1H)pyridinethionate) and 2-pyridinethiol-1-oxide sodium salt; phosphorus fungicides such as 0,0-diisopropyl S-benzylphosphorothioate and 0-ethyl S,S-diphenyldithiophosphate; phthalmide fungicides such as N-(2,6-p-diethylphenyl)phthalimide and N-(2,6-diethylphenyl)-4-methylphthalimide; dicarboxyimide fungicides such as N-trichloromethylthio 4-cyclohexene-1,2-dicarboxyimide and N-tetrachloroethylthio-4-cyclohexene-1,2-dicarboxyimide; oxathine fungicides such as 5,6-dihydro-2-methyl-1,4-oxathine-3-carboxanilido-4,4-dioxide and 5,6-dihydro-2-methyl-1, 4-oxathine-3-carboxanilide; naphthoquinone fungicides such as 2,3-dichloro-1,4-napththoquinone, 2-oxy-3-chloro-1,4-naphthoquinone copper sulfate; pentachloronitrobenzene; 1,4-dichloro-2,5-dimethoxybenzene; 5-methyl-s-triazol(3,4-b)benzthiazole; 2-(thiocyanomethylthio)benzothiazole; 3-hydroxy-5-methylisooxazole; N-2,3-dichlorophenyltetrachlorophthalamic acid; 5-ethoxy-3-trichloromethyl-1,2,4-thiadiazole; 2,4-dichloro-6-(0-chloroanilino)-1,3,5-triazine; 2,3-dicyano-1,4-dithioanthraquinone; copper 8-quinolinate; polyoxine; validamycin; cycloheximide; iron methanearsonate; diisopropyl 1,3-dithiolane-2-iridene malonate; 3-allyloxy-1,2-benzoisothiazol-1,1-dioxide; kasugamycin; Blasticidin S; 4,5,6,7-tetrachlorophthalide; 3-(3,5-dichlorophenyl)5-ethenyl-5-methyloxazolizine-2,4- dione; N-(3,5-dichlorophenyl)-1,2-dimethylcyclopropane-1,2-dicarboxyimide; S-n-butyl-5'-para-t-butylbenzyl-N-3-pyridyldithiocarbonylimidate; 4-chlorophenoxy-3,3-dimethyl-1-(1H,1,3,4-triazol-1-yl)-2-butanone; methyl-D,L-N-(2,6-dimethylphenyl)-N-(N'-methoxyacetyl)alaninate; N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]imidazol-1- carboxamide; N-(3,5-dichlorophenyl)succinamide; tetrachloroisophthalonitrile; 2-dimethylamino-4-methyl-5-n-butyl-6-hydroxypyrimidine; 2,6-dichloro-4-nitroaniline; 3-methyl-4-chlorobenzthiazol-2-one; 1,2,5,6-tetrahydro-4H-pyrrolol[3,2,1-i,j]quinoline-2-one; 3'-isopropoxy-2-methylbenzanilide; 1-[2-(2,4-dichlorophenyl)-4-ethyl-1-3-dioxorane-2-ylmethyl)hyl]-1H,1,2,4-triazol; 1,2-benzisothiazoline-3-one; basic copper chloride; basic copper sulfate; N'-dichlorofluoromethylthio-N,N-dimethyl-N-phenyl sulfamide; ethyl-N-(3-dimethylaminopropyl)thiocarbamate hydrochloride; piomycin; S,S-6-methylquinoxaline-2,3di-yldithiocarbonate; complex of zinc and manneb; di-zinc bis(dimethyldithiocarbamate)ethylenebis (dithicarbamate).
PLANT GROWTH REGULATORS AND HERBICIDES
Isourea plant growth regulators such as N-methoxycarbonyl-N'-methylphenylcarbamoylethylisourea and 1-(4-chlorophenylcarbamoyl)-3-ethoxycarbonyl-2-methylisourea; another type of plant growth regulators such as sodium naphthaleneacetate, 1,2-dihydropyridazine-3,-6-dione and gibberellins; triazine herbicides such as 2-methylthio-4,6-bisethylamino-1,3,5-triazine, 2-chloro-4,6-bisethylamino-1,3,5-triazine, 2-methoxy-4-ethylamino-6-isopropylamino-1,3,5-triazine, 2-chloro-4-ethylamino-6-isopropylamino-s-triazine, 2-methylthio-4,6-bis(isopropylamino)-S-triazine and 2-methylthio-4-ethylamino-6-isopropylamino-s-triazine; phenoxy herbicides such as 2,4-dichlorophenoxyacetic acid and methyl, ethyl, and butyl esters thereof. 2-chloro-4-methylphenoxyacetic acid, 4-chloro-2-methylphenoxyacetic acid and ethyl 2-methyl-4-chlorophenoxybutylate; diphenylether herbicides such as 2,4,6-trichlorophenyl-4'-nitrophenylether,2,4-dichlorophenyl-4'-nitrophenylether and 3,5-dimethylphenyl-4'-nitrophenylether; urea herbicides such as 3-(3,4-dichlorophenyl)-1-methoxy-1-methyl urea, 3-(3,4-dichlorophenyl)-1,1-dimethylurea and 3-(4-chlorophenyl)-1,1-dimethyl urea; carbamate herbicides such as 3-methoxycarbonylaminophenyl-N-(3-methylphenyl)carbamate, isopropyl-N-(3-chlorophenyl)carbamate and methyl-N-(3,4'-dichlorophenyl)carbamate; uracil herbicides such as 5-bromo-3-sec-butyl-6-methyluracil and 1-cyclohexyl-3,5-propyleneuracil; thiolcarbamate herbicides such as S-(4-chlorobenzyl)-N,N-diethylthiolcarbamate,S-ethyl-N-cyclohexyl-N-ethylthiolcarbamate and S-ethyl-hexahydro-1H-azepine-1-carbothioate and S-ethyl-N,N-di-n-propylthiocarbamate; pyridium herbicides such as 1,1'-di-methyl-4,4'-bispyridinium dichloride; phosphoric herbicides such as N-(phosphonomethyl)glycine; aniline herbicides such as alpha, alpha, alpha-trifluoro-2,6-dinitro-N,N-dipropyl-p-toluidine, 4-(methylsulfonyl)-2,6-dinitro-N,N-dipropylaniline and K<3>, N<3>-diethyl-2,4-dinitro-6-trifluoromethyl-1,3-phenylene diamine; acid anilide herbicides such as 2-chloro-2',6'-diethyl-N-(butoxymethyl)acetoanilide, 2-chloro-2',6'-diethyl-N-(methoxymethyl)acetoanilide, and 3,4-dichloropropioneanilide; pyrazole herbicides such as 1,3-dimethyl-4-(2,4-dichlorobenzoyl)-5-hydroxypyrazole and 1,3-di-methyl-4-(2,4-dichlorobenzoyl)-5-(p-toluenesulfonyloxy)pyrazole; 5-tert-butyl-3-(2,4-dichloro-5-isopropoxyphenyl)-1,3,4-oxadiazoline-2-one; 2-[N-isopropyl,N-(4-chlorophenyl)carbamoyl]-4-chloro-5methyl-4-isooxazoline-3-one; 3-isopropylbenzo-2-thia-1,3-diazinone-(4-2,4-dioxide and 3-(2-methyl-phenoxy)pyridazine.
INSECTICIDES
Phosphoric insecticides such as 0,0-diethyl O-(2-isopropyl-4-methyl-6-pyrimidinyl)phosphorothioate, 0,0-diethyl S-2-[(ethylthio)ethyl]phosphorodithioate, 0,0-dimethyl 0-(3-methyl-4-nitrophenyl)thiophosphate, 0,0-dimethyl S-(N-methylcarbamoylmethyl)phosphorodithioate, 0,0-dimethyl S-(N-methyl-N-formylcarbamoylmethyl)phosphorodithioate, 0,0-dimethyl S-2-[(ethylthio)ethyl]phosphorodithioate, 0,0-diethyl S-2-diethyl S-2-[(ethylthio)-ethyl]phosphorodithioate, 0,0-dimethyl-1-hydroxy-2,2,2-trichloroethylphosphonate, 0,0-diethyl-0-(5-phenyl-3-isooxazolyl)phosphorothioate, 0,0-dimethyl 0-(2,5-dichloro-4-bromophenyl)phosphorothioate, 0,0-dimethyl 0-(3-methyl-4-methylmercaptophenyl)thiophosphate, 0-ethyl 0-p-cyanophenyl phenylphosphorothioate,0,0-dimethyl-S-(1,2-dicarboethoxyethyl)phosphorodithioate, 2-chloro-(2,4,5-trichlorophenyl)vinyldimethyl phosphate, 2-chloro-1-(2,4-dichlorophenyl)vinyldimethyl phosphate, 0,0-dimethyl 0-p-cyanophenyl phosphorothioate, 2,2-di-chlorovinyl dimethyl phosphate, 0,0-diethyl 0-2,4-di-chlorophenyl phosphorothioate, ethyl mercaptophenylacetate 0,0-dimethyl phosphorodithioate, S-[(6-chloro-2-oxo-3-benzooxazolinyl)methyl]0,0-diethyl phosphorodithioate, 2-chloro-1-(2,4-dichlorophenyl)vinyl diethylphosphate 0,0-diethyl 0-(3-oxo-2-phenyl-2H-pyridazine-6-yl)phosphorothioate, 0,0-dimethyl S-(1-methyl-2-ethylsulfinyl)-ethyl phosphorothiolate, 0,0-dimethyl S-phthalimidomethyl phosphorodithioate, 0,0-diethyl 2,2,2-trichloroethanol, 2-(p-tert-butyl-phenoxy)isopropyl-2'-chloroethylsulfite, azoxybenzene, di-(p-chlorophenyl)-cyclopropyl carbinol, di[tri(2,2-dimethyl-2-phenylethyl)tin]oxide, 1-(4-chlorophenyl)-3-(2,6-difluorobenzoyl)urea and S-tricyclohexyltin 0,0-diisopropylphosphorodithioate.
INSECT REPELLENTS
The following insect repellents may be employed herein: 2-ethyl-1,3-hexanediol; N-octyl bicycloheptene dicarboximide; N,N-diethyl-M-toluamide; 2,3:4,5-Bis (2-butylene) tetrahydro-2-furaldehyde; Di-n-propyl isocinchomeronate; and 2-hydroxyethyl-n-octyl sulfide.
The active ingredients in the present invention are typically formulated so as to be present in the composition at from about 0.0001 percent to about 10 percent by weight; preferably from about 0.0005 percent to about 8 percent by weight. The end usage level of the products is therefore dependent upon the amount of the compositions of the present invention. It is thus within the skill of the applicator to determine the specific amount of active ingredient to be used in any particular application.
It is anticipated that the active ingredients herein will be utilized in their normal use level or slightly lower levels due to the enhanced effectiveness of the compositions of the present invention. The glycosides in the present invention will be utilized in the composition typically at from about 0.1 to about 20 percent; preferably from about 0.5 percent to about 10 percent by weight of the composition.
All matter of other adjuvants, powders, bulking agents and the like may be utilized in the present invention including dyes, foaming agents and additional solvents where required. Most typically, the compositions of the present invention will contain from about 5 percent to about 95 percent; preferably from about 10 percent to about 95 percent by weight water. Additional solvents may be added by the applicator to dilute out the composition. Of course, the products of the present invention may be formulated as aqueous products ready for use if desired. The products may be applied by aerial spraying, by in seed row application or with a fertilizer or the like.
The following is a suggested exemplification of the present invention.
EXAMPLE I
Wettable Powder
20 parts of 5-bromo-3-sec-butyl-6-methyluracil, 5 parts of lauryl glucoside (DP 2 average), 3 parts of calcium lignosulfonate and 72 parts of diatomaceous earth are mixed together and ground uniformly to give a wettable powder containing 20 percent by weight of the active ingredient compound.
EXAMPLE II
30 parts of 2,2-dichlorovinyl dimethyl phosphate, 50 parts of xylene and 20 parts of nonyl xyloside (DP 1.5 average) are mixed together to make a uniform solution, affording an emulsifiable concentrate containing 30 percent by weight of the active ingredient compound.
EXAMPLE III
Oily Formulation
50 parts of 3-methyl-4-chlorobenzthiazol-2-one and 50 parts of myristyl glucoside (DP 2.2 average) are mixed together to make a uniform mixture, affording an oily formulation containing 50 percent by weight of the active ingredient compound.
EXAMPLE IV
Sol (Flowable Powder)
40 parts of finely divided N-methoxycarbonyl-N'-4-methylphenylcarbamoylethylisourea having average particle size of not more than 10 microns, 4 parts of 2-ethylhexyl monoglucoside, 1 part of hydroxypropylcellulose and 55 parts of water are mixed together uniformly to give a sol containing 40 percent by weight of the active ingredient compound.
EXAMPLE V An insect repellent is prepared containing 1 part N,N-Diethyl-M-toluamide; 5 parts cetyl glucoside DP 2 average; and 94 parts octyl alcohol.

Claims (15)

What is claimed is:
1. A composition of matter comprising a plant growth regulator and an effective amount of a glycoside dispersing agent selected from the group consisting of fructoside, glucoside, mannoside, galactoside, taloside, guloside, alloside, altroside, idoside, arabinoside, xyloside, lyxoside and riboside and mixtures thereof in a sufficient amount to form an emulsion or dispersion of the active ingredient, said glycoside dispersing agent consisting essentially of glycosides corresponding to the formula:
R(OG)x
wherein R contains from 1 to 8 carbon atoms; O is an oxygen atom; x has an average value of from 1 to about 18; and G is the glycosyl portion of said glycoside dispersing agent.
2. The composition of claim 1 wherein G is glucoside.
3. The composition of claim 1 wherein x averages from about 1 to about 15.
4. The composition of claim 5 wherein x averages from about 1.2 to about 4.
5. The composition of claim 1 wherein x is 1.
6. The composition of claim 1 wherein G is glucose; and x is 1.
7. The composition of claim 1 wherein R is a branched alkyl moiety.
8. The composition of claim 1 wherein the active ingredient is present in the composition at from about 0.0001 percent to about 30 percent by weight.
9. The composition of claim 1 containing from about 20 percent to about 95 percent by weight of water.
10. The composition of claim 1 containing from about 0.1 percent to about 30 percent by weight of the glycoside.
11. The composition of claim 1 wherein R is a 2-ethylhexyl radical.
12. The composition of claim 11 wherein G is glucose.
13. The composition of claim 12 wherein x averages from about 1.2 to about 4.
14. The composition of claim 1 wherein the glycoside dispersing agent is 2-ethylhexyl monoglucoside.
15. The composition of claim 1 wherein the plant growth regulator is a herbicide.
US06/739,241 1985-05-30 1985-05-30 Glycoside-containing agricultural treatment composition Abandoned USH224H (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US06/739,241 USH224H (en) 1985-05-30 1985-05-30 Glycoside-containing agricultural treatment composition
US06/921,706 USH303H (en) 1985-05-30 1986-10-22 Glycoside-containing agricultural treatment composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US06/739,241 USH224H (en) 1985-05-30 1985-05-30 Glycoside-containing agricultural treatment composition

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US06/921,706 Division USH303H (en) 1985-05-30 1986-10-22 Glycoside-containing agricultural treatment composition

Publications (1)

Publication Number Publication Date
USH224H true USH224H (en) 1987-03-03

Family

ID=24971422

Family Applications (2)

Application Number Title Priority Date Filing Date
US06/739,241 Abandoned USH224H (en) 1985-05-30 1985-05-30 Glycoside-containing agricultural treatment composition
US06/921,706 Abandoned USH303H (en) 1985-05-30 1986-10-22 Glycoside-containing agricultural treatment composition

Family Applications After (1)

Application Number Title Priority Date Filing Date
US06/921,706 Abandoned USH303H (en) 1985-05-30 1986-10-22 Glycoside-containing agricultural treatment composition

Country Status (1)

Country Link
US (2) USH224H (en)

Cited By (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0364202A3 (en) * 1988-10-13 1991-10-09 Ici Australia Limited Herbicide composition
EP0526443A1 (en) * 1991-08-02 1993-02-03 Monsanto Company Herbicidal compositions and methods of preparing and using the same
US5258358A (en) * 1991-04-27 1993-11-02 Hoechst Aktiengesellschaft Liquid herbicidal compositions containing glufosinate and an alkyl polyglycoside
WO1993022917A1 (en) * 1992-05-14 1993-11-25 Henkel Corporation Alkyl glycoside compositions with improved wetting properties
WO1996008150A1 (en) * 1994-09-15 1996-03-21 Akzo Nobel N.V. Aqueous pesticidal microemulsion compositions
WO1996016540A1 (en) * 1994-12-01 1996-06-06 Henkel Corporation Biologically active composition
US5534043A (en) * 1994-03-15 1996-07-09 Heritage Environmental Services, Inc. Micronutrient supplement
US5658853A (en) * 1991-08-02 1997-08-19 Monsanto Company Glyphosate herbicidal compositions having enhanced rainfastness comprising an acetylenic diol and an alkyl polyglycoside
WO1998015181A1 (en) * 1996-10-07 1998-04-16 Zeneca Limited Glyphosate formulations
WO1999008517A1 (en) * 1997-08-18 1999-02-25 Cognis Deutschland Gmbh Microemulsions
WO1999012868A1 (en) * 1997-09-11 1999-03-18 Nonomura Arthur M Methods and compositions for enhancing growth of living organisms
WO1999048359A1 (en) * 1998-03-20 1999-09-30 Dow Agrosciences Llc Pesticidal adjuvants
WO2000007445A1 (en) * 1998-07-31 2000-02-17 Basf Aktiengesellschaft Aqueous growth-regulating compositions
US6248695B1 (en) 1996-12-06 2001-06-19 Huntsman Surfactants Technology Corporation Herbicidal compositions
US6258749B1 (en) 2000-02-22 2001-07-10 The Dow Chemical Company Methods for treating plants and enhancing plant growth using polyacylglycosides and/or polyalkylglycosides and formulations for same
WO2002003802A1 (en) * 2000-07-11 2002-01-17 Societe D'exploitation De Produits Pour Les Industries Chimiques (S.E.P.P.I.C.) Herbicide composition comprising glyphosate and at least a polyxyloside alkyl
US6358293B1 (en) 1999-11-23 2002-03-19 The Hampshire Chemical Corporation Methods for rendering high concentrations of manganese safe for plant growth and formulations for same
US20020098981A1 (en) * 1997-01-30 2002-07-25 Matthias Bratz Solid mixtures based on sulfonylureas and adjuvants
US6596779B1 (en) * 1999-02-10 2003-07-22 Agro Industrie Recherches Et Developpements Stable emulsion, process for the preparation thereof and agent for this purpose
US6746988B2 (en) 2001-09-07 2004-06-08 Syngenta Crop Protection, Inc. Surfactant systems for agriculturally active compounds
US20060142158A1 (en) * 2004-12-23 2006-06-29 Nonomura Arthur M Compositions and methods for anti-transpiration in plants
EP1854354A4 (en) * 2005-03-03 2010-10-13 Kao Corp Agent for enhancing antiseptic power
US8673865B2 (en) 2005-03-03 2014-03-18 Kao Corporation Agent for enhancing antiseptic power
US9828299B2 (en) 2012-05-21 2017-11-28 Innovation Hammer, Llc Methods for rendering micellar coordination complexes safe for the treatment of plants and formulations for same
US10010029B2 (en) 2011-11-21 2018-07-03 Innovation Hammer, Llc Methods and systems for growing plants using silicate-based substrates, cultivation of enhanced photosynthetic productivity and photosafening by utilization of exogenous glycopyranosides for endogenous glycopyranosyl-protein derivatives, and formulations, processes and systems for the same
US11013234B2 (en) 2016-04-29 2021-05-25 Innovation Hammer Llc Formulations and methods for treating photosynthetic organisms and enhancing qualities and quantities of yields with glycan composite formulations

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5230892A (en) * 1990-08-24 1993-07-27 Bayer Aktiengesellschaft Solid formulations
US5330674A (en) * 1992-09-09 1994-07-19 Henkel Corporation Method for increasing the efficiency of a disinfectant cleaning composition using alkyl polyglycosides
AU2380595A (en) * 1994-04-15 1995-11-10 Henkel Corporation Biologically active composition
US5516747A (en) * 1994-04-18 1996-05-14 Henkel Corporation Pesticidal surfactant mixtures comprising alkyl polyglycosides and alkyl naphthalene sulfonates
SE506265C2 (en) * 1995-04-28 1997-11-24 Akzo Nobel Nv Aqueous composition containing an alkyl glycoside and its use as a wetting agent
CN1960634A (en) * 2004-03-10 2007-05-09 孟山都技术公司 Herbicidal compositions containing N-phosphonomethyl glycine and an auxin herbicide
AR088560A1 (en) 2011-10-26 2014-06-18 Monsanto Technology Llc CARBOXYL ACID HERBICID SALTS
UY34845A (en) 2012-06-04 2014-01-31 Monsanto Technology Llc ? WATER CONCENTRATED HERBICIDE COMPOSITIONS CONTAINING GLIFOSATE SALTS AND DICAMBA SALTS
MX383384B (en) 2013-02-27 2025-03-13 Monsanto Technology Llc GLYPHOSATE COMPOSITION FOR TANK MIXES WITH DICAMBA WITH ENHANCED VOLATILITY.

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3219656A (en) 1963-08-12 1965-11-23 Rohm & Haas Alkylpolyalkoxyalkyl glucosides and process of preparation therefor
US3598865A (en) 1968-02-07 1971-08-10 Atlas Chem Ind Polyglycosides and process of preparing mono and polyglycosides
US4242120A (en) 1978-02-23 1980-12-30 Simferopolsky Gosudarstvenny Universitet Imeni M.V. Method for stimulating fructification and fruit growth of cultivated plants and gibberellin-based preparation for realizing same
US4512989A (en) 1981-10-15 1985-04-23 Hokko Chemical Industry Co., Ltd. 1,2,4-Triazole derivatives and fungicidal composition containing the same

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3219656A (en) 1963-08-12 1965-11-23 Rohm & Haas Alkylpolyalkoxyalkyl glucosides and process of preparation therefor
US3598865A (en) 1968-02-07 1971-08-10 Atlas Chem Ind Polyglycosides and process of preparing mono and polyglycosides
US4242120A (en) 1978-02-23 1980-12-30 Simferopolsky Gosudarstvenny Universitet Imeni M.V. Method for stimulating fructification and fruit growth of cultivated plants and gibberellin-based preparation for realizing same
US4512989A (en) 1981-10-15 1985-04-23 Hokko Chemical Industry Co., Ltd. 1,2,4-Triazole derivatives and fungicidal composition containing the same

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Chararas, "Phytochemical Relationships, etc.," (1980) CA 94:27777m (1981).
Schoenbeck et al, "Preformed Substances, etc.," (1976) CA 87:180607f (1977)

Cited By (42)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0364202A3 (en) * 1988-10-13 1991-10-09 Ici Australia Limited Herbicide composition
US5258358A (en) * 1991-04-27 1993-11-02 Hoechst Aktiengesellschaft Liquid herbicidal compositions containing glufosinate and an alkyl polyglycoside
EP0526443A1 (en) * 1991-08-02 1993-02-03 Monsanto Company Herbicidal compositions and methods of preparing and using the same
US5658853A (en) * 1991-08-02 1997-08-19 Monsanto Company Glyphosate herbicidal compositions having enhanced rainfastness comprising an acetylenic diol and an alkyl polyglycoside
WO1993022917A1 (en) * 1992-05-14 1993-11-25 Henkel Corporation Alkyl glycoside compositions with improved wetting properties
US5385750A (en) * 1992-05-14 1995-01-31 Henkel Corporation Alkyl glycoside compositions with improved wetting properties
US5534043A (en) * 1994-03-15 1996-07-09 Heritage Environmental Services, Inc. Micronutrient supplement
WO1996008150A1 (en) * 1994-09-15 1996-03-21 Akzo Nobel N.V. Aqueous pesticidal microemulsion compositions
WO1996016540A1 (en) * 1994-12-01 1996-06-06 Henkel Corporation Biologically active composition
US5559078A (en) * 1994-12-01 1996-09-24 Henkel Corporation Agriculturally active composition comprising polyhydroxy acid amide adjuvant
WO1998015181A1 (en) * 1996-10-07 1998-04-16 Zeneca Limited Glyphosate formulations
US6248695B1 (en) 1996-12-06 2001-06-19 Huntsman Surfactants Technology Corporation Herbicidal compositions
US9538757B2 (en) * 1997-01-30 2017-01-10 Basf Se Solid mixtures based on sulfonylureas and adjuvants
US20020098981A1 (en) * 1997-01-30 2002-07-25 Matthias Bratz Solid mixtures based on sulfonylureas and adjuvants
WO1999008517A1 (en) * 1997-08-18 1999-02-25 Cognis Deutschland Gmbh Microemulsions
US6255253B1 (en) 1997-08-18 2001-07-03 Cognis Deutschland Gmbh Microemulsions
WO1999012868A1 (en) * 1997-09-11 1999-03-18 Nonomura Arthur M Methods and compositions for enhancing growth of living organisms
WO1999048359A1 (en) * 1998-03-20 1999-09-30 Dow Agrosciences Llc Pesticidal adjuvants
WO2000007445A1 (en) * 1998-07-31 2000-02-17 Basf Aktiengesellschaft Aqueous growth-regulating compositions
US6451739B1 (en) 1998-07-31 2002-09-17 Basf Aktiengesellschaft Aqueous growth-regulating compositions
US6596779B1 (en) * 1999-02-10 2003-07-22 Agro Industrie Recherches Et Developpements Stable emulsion, process for the preparation thereof and agent for this purpose
US6358293B1 (en) 1999-11-23 2002-03-19 The Hampshire Chemical Corporation Methods for rendering high concentrations of manganese safe for plant growth and formulations for same
US6258749B1 (en) 2000-02-22 2001-07-10 The Dow Chemical Company Methods for treating plants and enhancing plant growth using polyacylglycosides and/or polyalkylglycosides and formulations for same
WO2002003802A1 (en) * 2000-07-11 2002-01-17 Societe D'exploitation De Produits Pour Les Industries Chimiques (S.E.P.P.I.C.) Herbicide composition comprising glyphosate and at least a polyxyloside alkyl
US6670306B2 (en) * 2000-07-11 2003-12-30 Société d'Exploitation de Produits pour les Industries Chimiques SEPPIC Herbicide composition comprising glyphosate and at least a polyxyloside alkyl
FR2811514A1 (en) * 2000-07-11 2002-01-18 Seppic Sa HERBICIDE COMPOSITION COMPRISING GLYPHOSATE AND AT LEAST ONE ALKYL POLYXYLOSIDE
US6746988B2 (en) 2001-09-07 2004-06-08 Syngenta Crop Protection, Inc. Surfactant systems for agriculturally active compounds
US9374955B2 (en) 2004-12-23 2016-06-28 Innovation Hammer, Llc Compositions and methods for anti-transpiration in plants
US20060142158A1 (en) * 2004-12-23 2006-06-29 Nonomura Arthur M Compositions and methods for anti-transpiration in plants
US8093182B2 (en) 2004-12-23 2012-01-10 Nonomura Arthur M Compositions and methods for anti-transpiration in plants
US9072304B2 (en) 2004-12-23 2015-07-07 Innovation Hammer, Llc Compositions and methods for anti-transpiration in plants
US9277697B2 (en) 2004-12-23 2016-03-08 Innovation Hammer, Llc Compositions and methods for anti-transpiration in plants
EP1854354A4 (en) * 2005-03-03 2010-10-13 Kao Corp Agent for enhancing antiseptic power
US8673865B2 (en) 2005-03-03 2014-03-18 Kao Corporation Agent for enhancing antiseptic power
US10010029B2 (en) 2011-11-21 2018-07-03 Innovation Hammer, Llc Methods and systems for growing plants using silicate-based substrates, cultivation of enhanced photosynthetic productivity and photosafening by utilization of exogenous glycopyranosides for endogenous glycopyranosyl-protein derivatives, and formulations, processes and systems for the same
US10517233B2 (en) 2011-11-21 2019-12-31 Innovation Hammer Llc Methods and systems for growing plants using silicate-based substrates, cultivation of enhanced photosynthetic productivity and photosafening by utilization of exogenous glycopyranosides for endogenous glycopyranosyl-protein derivatives, and formulations, processes and systems for the same
US11147219B2 (en) 2011-11-21 2021-10-19 Innovation Hammer, Llc Methods and systems for growing plants using silicate-based substrates, cultivation of enhanced photosynthetic productivity and photosafening by utilization of exogenous glycopyranosides for endogenous glycopyranosyl-protein derivatives, and formulations, process and systems for the same
US9828299B2 (en) 2012-05-21 2017-11-28 Innovation Hammer, Llc Methods for rendering micellar coordination complexes safe for the treatment of plants and formulations for same
US11013234B2 (en) 2016-04-29 2021-05-25 Innovation Hammer Llc Formulations and methods for treating photosynthetic organisms and enhancing qualities and quantities of yields with glycan composite formulations
US11122804B2 (en) 2016-04-29 2021-09-21 Innovation Hammer Llc Formulations and methods for treating photosynthetic organisms and enhancing qualities and quantities of yields with glycan composite formulations
US11968978B2 (en) 2016-04-29 2024-04-30 Innovation Hammer Llc Formulations and methods for treating photosynthetic organisms and enhancing qualities and quantities of yields with glycan composite formulations
US12317895B2 (en) 2016-04-29 2025-06-03 Innovation Hammer Llc Formulations and methods for treating photosynthetic organisms and enhancing qualities and quantities of yields with glycan composite formulations

Also Published As

Publication number Publication date
USH303H (en) 1987-07-07

Similar Documents

Publication Publication Date Title
USH224H (en) Glycoside-containing agricultural treatment composition
US5559078A (en) Agriculturally active composition comprising polyhydroxy acid amide adjuvant
US6068849A (en) Surfactants for use in agricultural formulations
US20060009360A1 (en) New adjuvant composition
EP1037528A1 (en) Agricultural adjuvant
US5550115A (en) Biologically active composition
US5674517A (en) Emulsifier for pesticide concentrates
US6156705A (en) Use of fatty alcohol polyalkoxy alkyl ethers in agricultural formulations
CA2311382A1 (en) Use of narrow range ethoxylates of fatty alcohols in agricultural pesticide and adjuvant formulations
EP1035770B1 (en) Use of fatty alcohol carbonates as solvents in agricultural formulations
US5928563A (en) Agricultural adjuvant
US6387960B1 (en) Agricultural formulations containing monoglycerides
AU1598199A (en) Agricultural formulations containing monoglycerides

Legal Events

Date Code Title Description
STCF Information on status: patent grant

Free format text: PATENTED CASE

AS Assignment

Owner name: HENKEL CORPORATION, 300 BROOKSIDE AVE., AMBLER, PA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:A.E. STALEY MANUFACTURING COMPANY;REEL/FRAME:004996/0815

Effective date: 19881123