EP1617720A1 - Herbizide zusammensetzungen, die glyphosate und ein pyridinanalog enthalten - Google Patents

Herbizide zusammensetzungen, die glyphosate und ein pyridinanalog enthalten

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Publication number
EP1617720A1
EP1617720A1 EP04760094A EP04760094A EP1617720A1 EP 1617720 A1 EP1617720 A1 EP 1617720A1 EP 04760094 A EP04760094 A EP 04760094A EP 04760094 A EP04760094 A EP 04760094A EP 1617720 A1 EP1617720 A1 EP 1617720A1
Authority
EP
European Patent Office
Prior art keywords
salt
carbon atoms
glyphosate
hydrocarbyl
independently
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.)
Ceased
Application number
EP04760094A
Other languages
English (en)
French (fr)
Inventor
Daniel R. Wright
Joseph J. Sandbrink
Paul G. Ratliff
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.)
Monsanto Technology LLC
Original Assignee
Monsanto Technology 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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=33311024&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP1617720(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Monsanto Technology LLC filed Critical Monsanto Technology LLC
Priority to EP13182598.6A priority Critical patent/EP2712503A3/de
Publication of EP1617720A1 publication Critical patent/EP1617720A1/de
Ceased legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION 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
    • A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
    • A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals

Definitions

  • the present invention relates generally to herbicidal compositions or formulations, and to methods of using such compositions to kill, or control the growth and proliferation of, unwanted plants.
  • the present invention relates to herbicidal compositions, as well as their methods of use, which comprise N- phosphonomethylglycine, or a herbicidal derivative thereof, and a pyridine analog, or a herbicidal derivative thereof, optionally with one or more suitable surfactants.
  • Such compositions cause early visual symptoms of treatment and/or enhanced effectiveness or control when applied to the foliage of plants.
  • Herbicidal compositions comprising the herbicide N-phosphonomethylglycine or derivatives thereof ("glyphosate"), are useful for suppressing the growth of, or killing, unwanted plants such as grasses, weeds and the like.
  • Glyphosate typically is applied to the foliage of the target plant. After application the glyphosate is absorbed by the foliar tissue of the plant and translocated throughout the plant. Glyphosate noncompetitively blocks an important biochemical pathway which is common to virtually all plants, but which is absent in animals.
  • glyphosate is very effective in killing or controlling the growth of unwanted plants, the uptake (i.e., absorption) of glyphosate by the plant foliar tissue and translocation of glyphosate throughout the plant is relatively slow. Visual symptoms that a plant has been treated with glyphosate may not appear until one week or more after treatment.
  • compositions comprising glyphosate may be formulated with one or more surfactants to enhance their effectiveness for foliar application.
  • surfactants such as polyoxyalkylene-type surfactants including, among other surfactants, polyoxyalkylene alkylamines.
  • Commercial formulations of glyphosate herbicide marketed under the trademark ROUNDUP® have been formulated by Monsanto with such a polyoxyalkylene alkylamine, in particular a polyoxyethylene tallowamine.
  • glyphosate As a result of the somewhat slow development of visual symptoms that may result when glyphosate is utilized alone, formulations or compositions containing glyphosate and another herbicide have been suggested, in an attempt to achieve both early visual symptoms of plant treatment and prolonged control of the plant.
  • a tank mix composition containing glyphosate and a contact herbicide such as a pyridine analog like triclopyr (i.e., [(3,5,6-trichloro-2-pyridinyl)oxy]acetic acid) or a herbicidal derivative thereof.
  • tank mixes have generally (i) employed relatively low weight ratios of glyphosate to, for example, triclopyr (wherein glyphosate and triclopyr are present in equal amounts, glyphosate is in a slight excess, or triclopyr is in excess), and/or (ii) not utilized a surfactant therein.
  • R.K. Howell et al. (Southern Weed Science Society Proceedings, 195-197 (1998)) disclose the preparation of a tank mixture containing a surfactant TL90, Roundup Pro® and GarlonTM 4, the glyphosate (in Roundup Pro®) and triclopyr (in GarlonTM 4) being present in an apparent weight ratio of approximately 1.3:1 , respectively.
  • G.M. Wright et al. disclose the preparation of a tank mixture of glyphosate and triclopyr in the apparent absence of a surfactant, the glyphosate and triclopyr, respectively, being present in an apparent weight ratio of approximately 1.5:1.
  • W. Harahap et al. disclose the preparation of tank mixtures of glyphosate and triclopyr or picloram, in the apparent absence of a surfactant.
  • glyphosate and triclopyr are, respectively, present in an apparent weight ratio of approximately 9.5:1 or 11.5:1
  • glyphosate and picloram are present in an apparent weight ratio of approximately 7.7:1.
  • a Roundup Pro® Supplemental Label (for application in California using a helicopter, EPA Reg. No. 524-475, Monsanto Company (1996)), discloses the optional preparation of a tank mixture of Roundup Pro® and GarlonTM 4 in varying weight ratios of glyphosate and triclopyr, respectively, as well as varying concentrations related thereto.
  • Tank mixtures require the user to purchase and store each herbicide used in the mixture separately, until the actual preparation of such mixtures in the field. The user must also measure out varying amounts of each herbicide used in the mixture. Therefore, a pre-packaged mixture (i.e., a concentrate) which already contains the desired herbicides in a single container may be desirable in some instances. However, concentrates may be difficult to prepare, for example when one of the herbicides is not soluble or miscible with the same desired solvent (e.g., water).
  • desired solvent e.g., water
  • a concentrated emulsion formulation consists of two phases and is a dispersion of one immiscible liquid (i.e., the discontinuous phase) in a second liquid (i.e., the continuous phase). If the continuous phase is water, the emulsion is an oil-in-water type emulsion and the water-immiscible liquid or solution may be referred to as the "oil" phase (regardless of its composition).
  • the active ingredient may be dissolved in an organic solvent along with added emulsifiers and/or dispersants.
  • the present invention is directed to an aqueous herbicidal liquid concentrate, which may be diluted with water to provide an aqueous herbicidal application mixture for application to the foliage of a plant.
  • the concentrate comprises glyphosate, or a herbicidal derivative thereof, in a concentration of at least about 50 grams acid equivalent per liter, a pyridine analog selected from the group consisting of triclopyr, clopyralid, dithiopyr and thiazopyr, or a herbicidal derivative thereof, and at least one surfactant, wherein (i) the glyphosate (acid equivalent basis) and the pyridine analog (acid equivalent basis) are present in a weight ratio of at least 1.7:1 , and (ii) when the glyphosate is predominantly in the form of a salt, said salt is selected from the group consisting of a sodium salt, an ammonium salt, an alkylammonium salt, a C 3 .
  • the present invention is further directed to an aqueous herbicidal liquid concentrate, which may be diluted with water to provide an aqueous herbicidal application mixture for application to the foliage of a plant.
  • the concentrate comprises glyphosate, or a herbicidal derivative thereof, in a concentration of at least about 50 grams acid equivalent per liter, a pyridine analog selected from the group consisting of triclopyr, clopyralid, dithiopyr, thiazopyr and picloram, or a herbicidal derivative thereof, and at least one surfactant, wherein (i) the glyphosate (acid equivalent basis) and the pyridine analog (acid equivalent basis) are present in a weight ratio ranging from at least 1.7:1 to less than about 32:1 , and (ii) when the glyphosate is predominantly in the form of a salt, said salt is selected from the group consisting of a sodium salt, an ammonium salt, an alkylammonium salt, a C 3 .
  • the present invention is still further directed to an aqueous herbicidal liquid concentrate, which may be diluted with water to provide an aqueous herbicidal application mixture for application to the foliage of a plant.
  • the concentrate comprises glyphosate, or a herbicidal derivative thereof, a pyridine analog selected from the group consisting of triclopyr, clopyralid, dithiopyr and thiazopyr, or a herbicidal derivative thereof, and at least one surfactant in a concentration ranging from about 1 grams to 283 grams per liter, wherein (i) the glyphosate (acid equivalent basis) and the pyridine analog (acid equivalent basis) are present in a weight ratio of at least 1 :1 , glyphosate being in excess, and (ii) when the glyphosate is predominantly in the form of a salt, said salt is selected from the group consisting of a sodium salt, an ammonium salt, an alkylammonium salt, a C 3 .
  • the present invention is still further directed to an aqueous herbicidal liquid concentrate, which may be diluted with water to provide an aqueous herbicidal application mixture for application to the foliage of a plant.
  • the concentrate comprises glyphosate, or a herbicidal derivative thereof, a pyridine analog selected from the group consisting of triclopyr, clopyralid, dithiopyr and thiazopyr, or a herbicidal derivative thereof, in a concentration ranging from about 1 gram to 99 grams (acid equivalent basis) per liter, and at least one surfactant, wherein (i) the glyphosate (acid equivalent basis) and the pyridine analog (acid equivalent basis) are present in a weight ratio of at least 1 :1 , glyphosate being in excess, and (ii) when the glyphosate is predominantly in the form of a salt, said salt is selected from the group consisting of a sodium salt, an ammonium salt, an alkylammonium salt, a
  • the present invention is still further directed to an aqueous herbicidal liquid concentrate, which may be diluted with water to provide an aqueous herbicidal application mixture for application to the foliage of a plant.
  • the concentrate comprises glyphosate, or a herbicidal derivative thereof, a pyridine analog selected from the group consisting of triclopyr, clopyralid, dithiopyr and thiazopyr, or a herbicidal derivative thereof, and at least one surfactant, wherein (i) the glyphosate (acid equivalent basis) and the pyridine analog (acid equivalent basis) are present in a weight ratio of at least 1 :1 , (ii) the glyphosate (acid equivalent basis) and the surfactant are present in a weight ratio of at least 1 :1 , wherein glyphosate is in excess in both instances, and (iii) when the glyphosate is predominantly in the form of a salt, said salt is selected from the group consisting of a sodium salt, an ammonium salt, an alkylammonium salt, a C 3 .
  • the present invention is still further directed to an aqueous herbicidal liquid concentrate, which may be diluted with water to provide an aqueous herbicidal application mixture for application to the foliage of a plant.
  • the concentrate comprises glyphosate, or a herbicidal derivative thereof, and a pyridine analog selected from the group consisting of triclopyr, clopyralid, dithiopyr and thiazopyr, or a herbicidal derivative thereof, wherein the glyphosate (acid equivalent basis) and the pyridine analog (acid equivalent basis) are present in a weight ratio of at least 1 :1 , glyphosate being in excess, and further wherein (i) the pyridine analog or a herbicidal derivative thereof is present at a concentration of not greater than 99 grams (acid equivalent) per liter, and (ii) when the glyphosate is predominantly in the form of a salt, said salt is selected from the group consisting of a sodium salt, an ammonium salt, an alkylammonium salt, a C 3 .
  • the present invention is still further directed to an aqueous herbicidal liquid concentrate, which may be diluted with water to provide an aqueous herbicidal application mixture for application to the foliage of a plant.
  • the concentrate comprises glyphosate, or a herbicidal derivative thereof, and a pyridine analog selected from the group consisting of triclopyr, clopyralid, dithiopyr and thiazopyr, or a herbicidal derivative thereof, wherein the glyphosate (acid equivalent basis) and the pyridine analog (acid equivalent basis) are present in a weight ratio of at least 1 :1 , glyphosate being in excess, and further wherein (i) the glyphosate (acid equivalent basis) or herbicidal derivative thereof is present at a concentration of not greater than 165 grams (acid equivalent) per liter, and (ii) when the glyphosate is predominantly in the form of a salt, said salt is selected from the group consisting of a sodium salt, an ammoni
  • the present invention is still further directed to an aqueous herbicidal liquid concentrate which may be diluted with water to provide an aqueous herbicidal application mixture for application to the foliage of a plant.
  • the concentrate comprises at least one glyphosate salt predominantly in the form of potassium glyphosate, monoethanolamine glyphosate, or a mixture thereof; a pyridine analog selected from the group consisting of triclopyr, clopyralid, fluroxypyr, dithiopyr and thiazopyr, or a herbicidal derivative thereof; and, at least one surfactant in a concentration less than 20 grams per liter; wherein the glyphosate (acid equivalent basis) and the pyridine analog (acid equivalent basis) are present in a weight ratio of at least 1 :1 , glyphosate being in excess.
  • the present invention is futher directed to an aqueous herbicidal liquid concentrate, which may be diluted with water to provide an aqueous herbicidal application mixture for application to the foliage of a plant.
  • the concentrate comprises glyphosate, or a herbicidal derivative thereof, in a concentration of less than 65 grams acid equivalent per liter, picloram, or a herbicidal derivative thereof, and at least one surfactant, wherein (i) the glyphosate (acid equivalent basis) and the picloram (acid equivalent basis) are present in a weight ratio of at least 1 :1 , with glyphosate being in excess.
  • said salt may be selected from the group consisting of a sodium salt, an ammonium salt, an alkylammonium salt, a C 3 . 16 alkanolammonium salt, a di- ammonium salt, an alkylamine salt, a C 3 . 16 alkanolamine salt, an alkylsulfonium salt, a sulfoxonium salt, and combinations thereof.
  • the present invention is still further directed to a method of killing or controlling weeds or unwanted vegetation.
  • the method comprises diluting one of the preceding liquid concentrates in a convenient amount of water to form an application mixture, and then applying a herbicidally effective amount of the application mixture to the foliage of the weeds or unwanted vegetation.
  • the present invention is still further directed to an aqueous herbicidal composition useful for killing or controlling the growth of unwanted plants.
  • the composition comprises glyphosate, or a herbicidal derivative thereof, a pyridine analog selected from the group consisting of triclopyr, clopyralid, fluroxypyr, dithiopyr and thiazopyr, or a herbicidal derivative thereof, and at least one surfactant, wherein (i) the glyphosate (acid equivalent basis) and the pyridine analog (acid equivalent basis) are present in a weight ratio of at least 7.6:1 , and (ii) when the glyphosate is predominantly in the form of a salt, said salt is selected from the group consisting of a sodium salt, an ammonium salt, an alkylammonium salt, a C 3 .
  • the present invention is still further directed to an aqueous herbicidal composition useful for killing or controlling the growth of unwanted plants.
  • the composition comprises glyphosate, or a herbicidal derivative thereof, a pyridine analog selected from the group consisting of triclopyr, clopyralid, dithiopyr and thiazopyr, or a herbicidal derivative thereof, in a concentration of not greater than 3.9 grams (acid equivalent basis) per liter, and at least one surfactant, wherein (i) the glyphosate (acid equivalent basis) and the pyridine analog (acid equivalent basis) are present in a weight ratio of at least about 1 :1 , glyphosate being in excess, and (ii) when the glyphosate is predominantly in the form of a salt, said salt is selected from the group consisting of a sodium salt, an ammonium salt, an alkylammonium salt, a C 3 .
  • the present invention is still further directed to an aqueous herbicidal composition useful for killing or controlling the growth of unwanted plants.
  • the composition comprises glyphosate, or a herbicidal derivative thereof, a pyridine analog selected from the group consisting of triclopyr, clopyralid, dithiopyr and thiazopyr, or a herbicidal derivative thereof, and at least one surfactant, wherein (i) the surfactant concentration is not greater than 3.9 grams per liter, (ii) glyphosate (acid equivalent basis) and the pyridine analog (acid equivalent basis) are present in a weight ratio of at least 3:1 , and (iii) when the glyphosate is predominantly in the form of a salt, said salt is selected from the group consisting of a sodium salt, an ammonium salt, an alkylammonium salt, a C 3 .
  • the present invention is still further directed to an aqueous herbicidal composition useful for killing or controlling the growth of unwanted plants.
  • the composition comprises glyphosate, or a herbicidal derivative thereof, a pyridine analog selected from the group consisting of triclopyr, clopyralid, fluroxypyr, dithiopyr and thiazopyr, or a herbicidal derivative thereof, and at least one surfactant, wherein (i) the surfactant concentration is not greater than 6.6 grams per liter, (ii) glyphosate (acid equivalent basis) and the pyridine analog (acid equivalent basis) are present in a weight ratio of at least 5:1 , and (iii) when the glyphosate is predominantly in the form of a salt, said salt is selected from the group consisting of a sodium salt, an ammonium salt, an alkylammonium salt, a C 3.16 alkanolammonium salt, a di- ammonium salt, an alkylamine salt, a
  • the present invention is still further directed to an aqueous herbicidal composition useful for killing or controlling the growth of unwanted plants.
  • the composition comprises glyphosate, or a herbicidal derivative thereof, a pyridine analog selected from the group consisting of triclopyr, clopyralid, fluroxypyr, dithiopyr and thiazopyr, or a herbicidal derivative thereof, and at least one surfactant, wherein (i) the surfactant concentration is not greater than 9.3 grams per liter, (ii) glyphosate (acid equivalent basis) and the pyridine analog (acid equivalent basis) are present in a weight ratio of at least 7:1 , and (iii) when the glyphosate is predominantly in the form of a salt, said salt is selected from the group consisting of a sodium salt, an ammonium salt, an alkylammonium salt, a C 3 .
  • the present invention is still further directed to an aqueous herbicidal composition useful for killing or controlling the growth of unwanted plants.
  • the composition comprises glyphosate or a herbicidal derivative thereof, a pyridine analog selected from the group consisting of triclopyr, clopyralid, fluroxypyr, dithiopyr and thiazopyr, or a herbicidal derivative thereof, and at least one surfactant, wherein either (i) the glyphosate concentration (acid equivalent basis) is not greater than 16.2 grams per liter, and glyphosate (acid equivalent basis) and the pyridine analog (acid equivalent basis) are present in a weight ratio of at least 4:1 , or (ii) the glyphosate concentration (acid equivalent basis) is not greater than 23.8 grams per liter, and glyphosate (acid equivalent basis) and the pyridine analog (acid equivalent basis) are present in a weight ratio of at least 6:1 , and further when the glyphosate is predominantly in the form of a salt, said salt is selected from the group consisting of a sodium salt, an ammonium salt, an alkylam
  • the present invention is still further directed to an aqueous herbicidal composition useful for killing or controlling the growth of unwanted plants.
  • the concentrate comprises at least one glyphosate salt predominantly in the form of potassium glyphosate, monoethanolamine glyphosate, or a mixture thereof; and a pyridine analog selected from the group consisting of triclopyr, clopyralid, fluroxypyr, dithiopyr and thiazopyr, or a herbicidal derivative thereof; wherein (i) the glyphosate salt is present in a concentration less than 180 grams acid equivalent per liter and the glyphosate salt (acid equivalent basis) and the pyridine analog (acid equivalent basis) are present in a weight ratio of at least 1 :1 , glyphosate being in excess; (ii) the glyphosate salt is present in a concentration less than 240 grams acid equivalent per liter and the glyphosate salt (acid equivalent basis) and the pyridine analog (acid equivalent basis) are present in a weight ratio of at least 2:1 ; (iii) the glyphosate salt is present in a concentration less than 270
  • the present invention is still further directed to a method for killing or controlling the growth of unwanted plants.
  • the method comprises contacting the foliage of said plants with a herbicidally effective amount of one of the previously described aqueous herbicidal compositions.
  • the present invention is still further directed to a herbicidal particulate solid concentrate which may be dissolved or dispersed in water to provide an aqueous herbicidal application mixture for application to the foliage of a plant.
  • the solid concentrate comprises glyphosate, or a herbicidal derivative thereof, and a pyridine analog, or a herbicidal derivative thereof, wherein a weight ratio (a.e.
  • glyphosate to the pyridine analog is at least about 1 :1 , glyphosate being in excess, and further wherein when the glyphosate is predominantly in the form of a salt.
  • one or more surfactants may be present in the herbicidal particulate solid concentrate.
  • the present invention is still further directed to a method of killing or controlling weeds or unwanted vegetation. The method comprises diluting or dissolving the previously described solid particulate concentrate in a convenient amount of water to form an application mixture, and then applying a herbicidally effective amount of the application mixture to the foliage of the weeds or unwanted vegetation.
  • the present invention is still further directed to one or more of the previously noted methods for killing or controlling the growth of unwanted plants which comprises contacting the foliage of said plants with such an aqueous herbicidal composition, wherein said herbicidal composition is brought into contact with, or applied to, said foliage using means other than a helicopter.
  • the present invention is still further directed to a method of killing or controlling weeds or unwanted plants.
  • the method comprises diluting an aqueous herbicidal concentrate composition in an amount of water to form an application mixture; and, applying a herbicidally effective amount of the application mixture to foliage of the weeds or unwanted plants, wherein the weeds or unwanted plants comprise poison ivy, poison oak, kudzu, multiflora rose, golden rod, blue fescue, red maple, and/or red oak, and the aqueous herbicidal concentrate composition comprises glyphosate or a herbicidal derivative thereof; a pyridine analog selected from the group consisting of triclopyr, clopyralid, dithiopyr, thiazopyr and picloram, or a herbicidal derivative thereof; and, at least one surfactant.
  • the present invention is still further directed to one or more of the previously described aqueous herbicidal liquid concentrates, aqueous herbicidal compositions, herbicidal particulate solid concentrates, and methods for the use thereof, wherein said pyridine analog is triclopyr, a derivative thereof, or some combination which includes triclopyr.
  • the present invention is still further directed to one or more of the previously described aqueous herbicidal liquid concentrates, aqueous herbicidal compositions, herbicidal particulate solid concentrates, and methods for the use thereof, wherein said pyridine analog is clopyralid, a derivative thereof, or some combination which includes clopyralid.
  • the present invention is still further directed to one or more of the previously described aqueous herbicidal liquid concentrates, aqueous herbicidal compositions, herbicidal particulate solid concentrates, and methods for the use thereof, wherein said pyridine analog is dithiopyr, a derivative thereof, or some combination which includes dithiopyr.
  • the present invention is still further directed to one or more of the previously described aqueous herbicidal liquid concentrates, aqueous herbicidal compositions, herbicidal particulate solid concentrates, and methods for the use thereof, wherein said pyridine analog is thiazopyr, a derivative thereof, or some combination which includes thiazopyr.
  • the present invention is still further directed, where appropriate, to one or more of the previously described aqueous herbicidal liquid concentrates, aqueous herbicidal compositions, herbicidal particulate solid concentrates, and methods for the use thereof, wherein said pyridine analog is picloram, a derivative thereof, or some combination which includes picloram.
  • the present invention is still further directed, where appropriate, to one or more of the previously described aqueous herbicidal liquid concentrates, aqueous herbicidal compositions, herbicidal particulate solid concentrates, and methods for the use thereof, wherein said pyridine analog is fluroxypyr, a derivative thereof, or some combination which includes fluroxypyr.
  • the present invention is still further directed, where appropriate, to one or more of the previously described aqueous herbicidal liquid concentrates, aqueous herbicidal compositions, herbicidal particulate solid concentrates, and methods for the use thereof, wherein said pyridine analog is a combination or mixture of one or more of triclopyr, fluroxypyr, dithiopyr, thiazopyr, picloram, or derivatives thereof.
  • the present invention is still further directed, where appropriate, to one or more of the previously described aqueous herbicidal liquid concentrates, aqueous herbicidal compositions, herbicidal particulate solid concentrates, and methods for the use thereof, wherein said pyridine analog is a combination or mixture of triclopyr and clopyralid, or derivatives thereof.
  • the present invention is still further directed, where appropriate, to one or more of the previously described aqueous herbicidal liquid concentrates, aqueous herbicidal compositions, herbicidal particulate solid concentrates, and methods for the use thereof, wherein said pyridine analog is a combination or mixture of one or more of triclopyr, clopyralid, fluroxypyr, or derivatives thereof.
  • coherbicidal compositions or formulations containing glyphosate or a derivative thereof, a pyridine analog (e.g., triclopyr, clopyralid, fluroxypyr, dithiopyr, thiazopyr, picloram, etc., or a combination thereof) or a derivative thereof, and optionally a suitable surfactant are provided that are advantageous for a number of reasons, including rapid uptake by the target plant, early visual symptoms of plant treatment, and control of a broad spectrum of plant species, as well as enhanced, more consistent control of unwanted plants.
  • lower application rates may potentially be used for the pyridine analog and/or the surfactant(s) applied, without a loss of effectiveness of plant control.
  • compositions or formulations of the present invention comprise at least two herbicides, and optionally at least one surfactant.
  • a first component of the compositions of the present invention may be, for example, N-phosphonomethylglycine ("glyphosate”), a salt or adduct thereof, or a compound which is converted to glyphosate in plant tissues or which otherwise provides glyphosate ion.
  • glyphosate N-phosphonomethylglycine
  • glyphosate N-phosphonomethylglycine
  • salt or adduct thereof or a compound which is converted to glyphosate in plant tissues or which otherwise provides glyphosate ion.
  • glyphosate when used herein, is to be understood to encompass such derivatives unless the context requires otherwise.
  • Glyphosate salts that can be used according to this invention include but are not restricted to, for example, alkali metal salts, for example sodium and potassium salts, ammonium salts, alkylammonium salts (e.g., C,_ 16 alkylammonium, or alternatively C 3 . 16 alkylammonium), alkanolammonium salts (e.g., C,. ⁇ alkanolammonium, or alternatively C 3 . 16 alkanolammonium), di-ammonium salts such as dimethylammonium, alkylamine salts, for example dimethylamine and isopropylamine salts, alkanolamine salts (e.g., C,.
  • alkali metal salts for example sodium and potassium salts
  • ammonium salts e.g., alkylammonium salts (e.g., C,_ 16 alkylammonium, or alternatively C 3 . 16 alkylammonium)
  • 16 alkanolamine or alternatively C 3 . 16 alkanolamine
  • ethanolamine salts for example ethanolamine salts, alkylsulfonium salts (e.g., C ⁇ e alkylsulfonium, for example trimethylsulfonium salts), sulfoxonium salts, and mixtures or combinations thereof.
  • alkylsulfonium salts e.g., C ⁇ e alkylsulfonium, for example trimethylsulfonium salts
  • sulfoxonium salts and mixtures or combinations thereof.
  • preferred glyphosate salts include for example the potassium salt, isopropylamine salt, ammonium salt, di-ammonium salt, sodium salt, monoethanolamine salt, and trimethylsulfonium salt, as well as combinations thereof.
  • glyphosate is predominantly in the form of a salt other than a potassium salt or a monoethanolamine or monoethanolammonium salt; that is, in an alternative preferred embodiment glyphosate is a salt predominantly in the form of the isopropylamine salt, the ammonium salt, the di-ammonium salt, the sodium salt, the trimethylsulfonium salt, or some combination thereof.
  • N-phosphonomethylglycine The herbicidal properties of N-phosphonomethylglycine and its derivatives were first discovered by Franz, then disclosed and patented in U.S. Patent No. 3,799,758, issued March 26, 1974. A number of herbicidal salts of N-phosphonomethylglycine were patented by Franz in U.S. Patent No. 4,405,531 , issued September 20, 1983. The disclosures of both of these patents are hereby incorporated by reference.
  • Various salts of N-phosphonomethylglycine are commercially significant, in part because they are water soluble. Many of the salts listed herein are highly water soluble, thereby allowing for highly concentrated solutions that can be diluted at the site of use.
  • a solution containing a herbicidally effective amount of glyphosate, and other components as described elsewhere herein e.g., a pyridine analog, and optionally a surfactant
  • a pyridine analog or derivative thereof i.e., an acid, a salt or an ester form thereof
  • U.S. Patent No. 4,692,184 which is incorporated in its entirety herein by reference for all relevant purposes
  • pyridine analogs is intended to generally refer to a class of herbicides that includes, for example: triclopyr (i.e., [(3,5,6-trichloro-2-pyridinyl)oxy]acetic acid), clopyralid (i.e., 3,6-dichloro-2-pyridine carboxylic acid), fluroxypyr (i.e., [(4-amino-3,5-dichoro-6-fluoro-pyridyl)oxy]aetic acid), dithiopyr (i.e., S,S-dimethylester-2-(difluoromethyl)-4-(2-methylpropyl)-6- (trifluoromethyl)-3,5-pyridine dicarbothioic acid), thiazopyr (i.e., methyl 2- (difluoromethyl)-5-(4,5-dihydro-2-thiazolyl)-4-(2-methylpropyl)-6-(
  • the present invention encompasses essentially any formulation disclosed herein (e.g., concentrate, solid or tank mix) which comprises glyphosate and any one of triclopyr, clopyralid, fluroxypyr, dithiopyr, thiazopyr, picloram, or a derivative thereof, as well as any combination or mixture which includes any one, two, there, four, five or six of these pyridine analogs.
  • formulation disclosed herein e.g., concentrate, solid or tank mix
  • the pyridine analog is selected from the group consisting of triclopyr, clopyralid, dithiopyr, thiazopyr, picloram, or some combination thereof.
  • the pyridine analog is selected from the group consisting of triclopyr, clopyralid, dithiopyr, thiazopyr, or some combination thereof.
  • the pyridine analog is selected from the group consisting of triclopyr, clopyralid, dithiopyr, or some combination thereof.
  • the pyridine analog is selected from the group consisting of triclopyr, clopyralid, or a combination thereof.
  • the pyridine analog is selected from the group consisting of triclopyr, dithiopyr, thiazopyr, or some combination thereof. In yet another preferred embodiment, the pyridine analog is selected from the group consisting of triclopyr, clopyralid, fluroxypyr, or some combination thereof.
  • ester and salt forms of the pyridine analogs or derivatives thereof of the present invention encompasses essentially any such ester or salt known to one of ordinary skill in the art, or which may be prepared thereby using techniques known in the art.
  • Exemplary salts may include alkali metal salts, for example sodium and potassium salts, ammonium salts, alkylammonium salts (e.g., C ⁇ alkylammonium), alkanolammonium salts (e.g., C ⁇ 6 alkanolammonium), di-ammonium salts such as dimethylammonium, alkylamine salts, for example dimethylamine and isopropylamine salts, alkanolamine salts, for example ethanolamine salts, alkylsulfonium salts (e.g., C ⁇ alkylsulfonium, for example trimethylsulfonium salts), sulfoxonium salts, and mixtures or combinations thereof.
  • alkali metal salts for example sodium and potassium salts, ammonium salts, alkylammonium salts (e.g., C ⁇ alkylammonium), alkanolammonium salts (e.g., C ⁇ 6 alkanolammonium
  • glyphosate and the pyridine analog e.g., triclopyr, clopyralid, fluroxypyr, dithiopyr, thiazopyr, picloram, etc., or a combination thereof
  • a contemplated herbicidal composition i.e., a particulate solid 5 concentrate, or liquid concentrate, or alternatively a ready-to-use, or tank-mix, composition
  • concentrations of these herbicides, and optionally a surfactant and/or some other additive as described elsewhere herein
  • 10 of the invention is sufficient to provide at least about 70% control (as determined by means known in the art) within about 50 days, preferably about 40 days, more preferably about 30 days, still more preferably about 20 days, still more preferably about 15 days, still more preferably about 10 days, still more preferably about 5 days, and even still more preferably about 1 day, or less, after application of the
  • the concentration of these herbicides, and optionally a surfactant and/or some other additive, in the herbidical compositions of the invention is sufficient to provide at least about 80%, more preferably at least about 85%, still more preferably at least about 90%, and still more preferably at least about 95%, control, or more, within about 50 days, preferably
  • 20 about 40 days, more preferably about 30 days, still more preferably about 20 days, still more preferably about 15 days, still more preferably about 10 days, still more preferably about 5 days, and even still more preferably about 1 day, or less, after application of the composition to a plant.
  • 25 surfactant and/or some other additive (as described elsewhere herein), in the herbicidal compositions of the invention is sufficient to provide at least about 70% control of plant regrowth (as determined by means known in the art) for at least about 20, preferably at least about 30, more preferably at least about 40, still more preferably at least about 50, still more preferably at least about 60, still more
  • the concentrations of these herbicides, and optionally a surfactant and/or some other additive, in the herbidical compositions of the invention is sufficient to provide at least about 80%, more preferably at least about
  • the glyphosate concentration may be at least about 50 grams, preferably at least about 75 grams, more preferably at least about 100 grams, still more preferably at least about 125 grams, still more preferably at least about 150 grams, still more preferably at least about 175 grams, still more preferably at least about 200 grams, still more preferably at least about 225 grams, still more preferably at least about 250 grams, (acid equivalent) per liter, or more (e.g., at least about 300 grams, at least about 350 grams, at least about 400 grams, at least about 450 grams, at least about 500 grams, at least 550 grams, at least 600 grams per liter, or more).
  • the glyphosate concentration may therefore range from, for example, about 50 to about 500 grams (a.e.) per liter, from about 100 to about 400 grams per liter, from about 150 to about 300 grams per liter, or from about 175 to about 250 grams per liter.
  • the concentration of glyphosate may be no greater than 165 grams per liter (e.g., no greater than 160 grams per liter, 155 grams per liter, 150 grams per liter, 140 grams per liter, or even no greater than about 130, about 120, about 110, about 100, about 75 grams per liter or less).
  • the glyphosate concentration may therefore range, for example, from about 100 to no greater than 160 grams per liter, or from about 110 to no greater than 150 grams per liter.
  • the glyphosate concentration may be less than about 50, preferably less than about 45, more preferably less than about 40, still more preferably less than about 35, still more preferably less than about 30, or even still more preferably less than about 25 grams (a.e.) per liter (e.g., about 2, about 4, about 6, about 8, about 10, about 12, about 14, about 16, about 18 or about 20 grams (a.e.) per liter).
  • the glyphosate concentration may range, for example, from about 2 to about 50 grams (a.e.) per liter, from about 4 to about 25, from about 6 to about 15, or from about 8 to about 12 grams (a.e.) per liter. In some instances, such as wherein:
  • the concentration of glyphosate may be no greater than 16.2 grams (a.e.) per liter (e.g., no greater than about 16, about 15.5, about 15, about 14.5, about 14, about 13.5, about 13, about 12.5, about 12, about 11.5, about 11 , about 10.5, about 10, about 9.5, about 9, about 8.5, about 8, about 7.5, about 7, about 6.5, about 6, about 5.5, about 5, etc., the concentration thus ranging from, for example, about 5 to about 16, from about 7 to about 14, or from about 8 to about
  • the weight ratio (a.e. to a.e.) of glyphosate to pyridine analog is at least 6:1 (e.g., at least about 7:1 , 8:1 , 9:1 , 10:1 , 11 :1 , 12:1 , 13:1 , 14:1 , 15:1 , 20:1 , 40:1 , 60:1 , 80:1 , or even 100:1 ), the concentration of glyphosate may be no greater than 23.8 grams (a.e.) per liter (e.g., no greater than about 23.5, about 23, about 22.5, about 22, about 21.5, about 21 , about 20.5, about 20, about 19.5, about 19, about 18.5, about 18, about 17.5, about 17, about 16.5, about 16, about 15.5, about 15, about 14.5, about 14, about 13.5, about 13, about 12.5, about 12, about 11.5, about 11 , about 10.5, about 10, about 9.5, about 9, about 8.5, about 8, about 7.5, about 7, about 6.5, about 6,
  • the concentration of one or more other ingredients in the present composition may be reduced to maintain the solubility of one or more of the ingredients therein (i.e., to ensure these ingredients remain in solution).
  • the concentration of the pyridine analog in the herbicidal composition of the present invention may also vary.
  • the concentration may preferably be sufficient to provide visual symptoms of herbicide treatment within about 5 days, preferably about 4 days, or more preferably about 3 days after application of the composition to the plant, and in some instances may be sufficient to provide such symptoms within about 2 days, about 1 day or even less, after the application.
  • the concentration of the pyridine analog is also preferably controlled, such that it is not substantially antagonistic to the herbicidal activity of the glyphosate, or glyphosate derivative, within the composition.
  • the concentration of the pyridine analog may be, for example, at least about 1 , about 2, about 4, about 6, about 8, about 10, about 15, about 20, about 25, about 30, about 35, about 40, about 45, about 50, about 60, about 70, about 80, about 90, about 100 or more grams (a.e.) per liter.
  • the concentration of the pyridine analog may therefore range, for example, from about 1 to about 99 or 100 grams (a.e.) per liter (e.g., about 1 to about 99 or 100, about 2 to about 80, about 4 to about 60, about 6 to about 40, or about 8 to about 20, grams (a.e.) per liter).
  • the concentration may alternatively be not greater than 99 grams (a.e.) per liter (e.g., not greater than about 95, about 90, about 85, about 80, about 75, about 70, about 65, about 60, about 55, about 50, about 40, about 30, about 20, about 10, about 5 or less grams (a.e.) per liter).
  • the concentration of the pyridine analog may range from, for example, about 1 to less than 99 grams (a.e.) per liter (e.g., from about 2 to less than about 80, from about 4 to less than about 60, from about 6 to less than about 40, or from about 8 to less than about 20, grams (a.e.) per liter).
  • the concentration of the pyridine analog may be less than about 25, about 15 or even about 10 grams (a.e.) liter, the concentration ranging for example from about 0.2 to about 10 grams (a.e.) per liter, from about 0.4 to about 6, from about 0.6 to about 4, or from about 0.8 to about 2 grams (a.e.) per liter.
  • the concentration of the pyridine analog may be not greater than 3.9 grams (a.e.) per liter (e.g., not greater than about 3.8, about 3.7, about 3.6, about 3.5, about 3.4, about 3.3, about 3.2, about 3.1 , about 3, about 2.8, about 2.6, about 2.4, about 2.2, about 2, about 1.8, about 1.6, about 1.4, about 1.2, about 1 , about 0.8, about 0.6, about 0.4, about 0.2 grams (a.e.) per liter or less, the concentration ranging for example from about 0.2 to about 3.5 grams (a.e.) per liter, from about 0.4 to about 3, from about 0.6 to about 2.5, or from about 0.8 to about 2 grams (a.e.) per liter).
  • weight ratio (a.e. to a.e.) of glyphosate to the pyridine analog, generally speaking this is greater than about 1 :1 (i.e., glyphosate is in excess); that is, this ratio may be at least about 1.1 :1 , about 1.2:1 , about 1.3:1 , about 1.4:1 , about 1.5:1 , about 1.6:1 , about 1.7:1 , about 1.8:1 , about 1.9:1 , about 2:1 , about 2.2:1 , about 2.4:1 , about 2.6:1 , about 2.8:1 , about 3:1 , about 4:1 , about 5:1.
  • this ratio may range from about 1 :1 to about 100:1 , from about 2:1 to about 80:1 , from about 4:1 to about 60:1 , from about 6:1 to about 40:1 , or from about 8:1 to about 20:1.
  • this ratio may be at least 7.6:1 , and preferably may be at least about 7.7:1 , about 7.8:1 , about 7.9:1 , about 8:1 , about 8.2:1 , about 8.4:1 , about 8.6:1 , about 8.8:1 , about 9:1 , about 9.2:1 , about 9.4:1 , about 9.6:1 , about 9.8:1 , about 10:1 or more (e.g., about 11 :1 , about 12:1 , about 13:1 , about 14:1 , about 15:1 , about 20:1 , about 25:1 , about 30:1 , about 35:1 , about 40:1 , about 45:1 , about 50:1 , about 60:1 , about 70:1 , about 80:1 , about 90:1 or even about 100:1 ). Accordingly, this ratio ranges from, for
  • the ratio of glyphosate to pyridine analog may be greater than about 1 :1 and less than about 32:1 , range for example from about 5:1 to about 30:1 , from about 10:1 to about 25:1 , from about 11 :1 to about 20:1 , from about 12:1 to about 18:1 , or from about 14:1 to about 16:1.
  • the concentration of glyphosate may be other than herein described without departing from the scope of the present invention.
  • each concentration, concentration range, ratio, etc. noted herein is intended to apply independently triclopyr, clopyralid, fluroxypyr, dithiopyr, thiazopyr, picloram, etc., or a combination thereof.
  • glyphosate compositions or formulations include, for example:
  • R 1 and R 2 are hydrocarbyl having from 1 to about 30 carbon atoms
  • R 3 is hydrogen or hydrocarbyl having from 1 to about 30 carbon atoms.
  • preferred R 1 , R 2 , and R 3 hydrocarbyl groups are linear or branched alkyl, linear or branched alkenyl, linear or branched alkynyl, aryl, or aralkyl groups.
  • R 1 is a linear or branched alkyl or linear or branched alkenyl group having from about 8 to about 30 carbon atoms
  • R 2 and R 3 are independently hydrogen or a linear or branched alkyl or linear or branched alkenyl group having from 1 to about 6 carbon atoms.
  • R 1 is a linear or branched alkyl group having from about 12 to about 22 carbon atoms
  • R 2 and R 3 are independently hydrogen, methyl, ethyl, or linear or branched hydroxyalkyl groups having from 1 to about 6 carbon atoms.
  • the surfactant may have the formula (1 ) wherein R 1 is hydrocarbyl or substituted hydrocarbyl having from about 8 to about 30 carbon atoms, R 2 is a hydroxyalkyl, polyhydroxyalkyl or poly(hydroxyalkyl)alkyl group, and R 3 is hydrogen, hydroxyalkyl, polyhydroxyalkyl or poly(hydroxyalkyl)alkyl.
  • R 1 hydrocarbyl groups are linear or branched alkyl, linear or branched alkenyl, linear or branched alkynyl, aryl, or aralkyl groups.
  • R 1 is a linear or branched alkyl, linear or branched alkenyl, linear or branched alkynyl, aryl, or aralkyl group having from about 8 to about 30 carbon atoms
  • R 2 is a linear or branched hydroxyalkyl group having from 1 to about 6 carbon atoms
  • R 3 is hydrogen or a linear or branched hydroxyalkyl group having from 1 to about 6 carbon atoms.
  • R 1 is a linear or branched alkyl, linear or branched alkenyl, linear or branched alkynyl, aryl, or aralkyl group having from about 8 to about 22 carbon atoms
  • R 2 is a linear or branched hydroxyalkyl group having from 1 to about 4 carbon atoms
  • R 3 is hydrogen or a linear or branched hydroxyalkyl group having from 1 to about 4 carbon atoms.
  • R 1 is a linear or branched alkyl, linear or branched alkenyl, linear or branched alkynyl, aryl, or aralkyl group having from about 8 to about 18 carbon atoms
  • R 2 is hydroxymethyl or hydroxyethyl
  • R 3 is hydrogen, hydroxymethyl or hydroxyethyl.
  • R 1 and R 4 are independently hydrocarbyl or substituted hydrocarbyl groups having from 1 to about 30 carbon atoms or -R 5 SR 6
  • R 2 in each of the x (R 2 O) groups is independently C 2 -C 4 alkylene
  • R 3 is hydrogen, or a linear or branched alkyl group having from 1 to about 4 carbon atoms
  • R 5 is a linear or branched alkyl group having from about 6 to about 30 carbon atoms
  • R 6 is a hydrocarbyl or substituted hydrocarbyl group having from 4 to about 15 carbon atoms
  • x is an average number from 1 to about 60.
  • R 1 , R 4 , and R 6 hydrocarbyl groups are linear or branched alkyl, linear or branched alkenyl, linear or branched alkynyl, aryl, or aralkyl groups.
  • R 1 includes from about 7 to about 30 carbon atoms, preferably from about 8 to about 22 carbon atoms, and the remaining groups are as described above.
  • R 1 and R 4 are independently a linear or branched alkyl or linear or branched alkenyl group having from 1 to about 25 carbon atoms
  • R 2 in each of the x (R 2 O) groups is independently C 2 -C 4 alkylene
  • R 3 is hydrogen, methyl or ethyl
  • x is an average number from 1 to about 40.
  • R 1 and R 4 are independently a linear or branched alkyl group having from 1 to about 22 carbon atoms
  • R 2 in each of the x (R 2 O) groups is independently ethylene or propylene
  • R 3 is hydrogen or methyl
  • x is an average number from 1 to about 30.
  • R 1 is a linear or branched alkyl group having from about 8 to about 22 carbon atoms and R 4 is a linear or branched alkyl group having from 1 to about 22 carbon atoms
  • R 2 in each of the x (R 2 O) groups is independently ethylene or propylene
  • R 3 is hydrogen or methyl
  • x is an average number from about 1 to about 10.
  • R 1 is a linear or branched alkyl group having from about 16 to about 22 carbon atoms and R 4 is methyl
  • R 2 in each of the x (R 2 O) groups is ethylene
  • R 3 is hydrogen
  • x is an average number from about 1 to about 5
  • R 1 is a linear or branched alkyl group having from about 8 to about 15 carbon atoms and R 4 is methyl
  • R 2 in each of the x (R 2 O) groups is ethylene
  • R 3 is hydrogen
  • x is an average number from about 5 to about 10.
  • R 1 is hydrocarbyl or substituted hydrocarbyl having from 1 to about 30 carbon atoms
  • R 2 in each of the x (R 2 O) and y (R 2 O) groups is independently C 2 -C alkylene
  • R 3 is hydrogen, or a linear or branched alkyl group having from 1 to about 4 carbon atoms
  • R 4 is hydrogen or hydrocarbyl or substituted hydrocarbyl having from 1 to about 30 carbon atoms
  • x and y are independently an average number from 1 to about 40
  • X- is an agriculturally acceptable anion.
  • R 1 and R 4 hydrocarbyl groups are linear or branched alkyl, linear or branched alkenyl, linear or branched alkynyl, aryl, or aralkyl groups.
  • R 1 and R 4 are independently a linear or branched alkyl or linear or branched alkenyl group having from 1 to about 25 carbon atoms
  • R 2 in each of the x (R 2 O) and y (R 2 O) groups is independently C 2 -C 4 alkylene
  • R 3 is hydrogen, methyl or ethyl
  • the sum of x and y is an average number from about 2 to about 30.
  • R 1 and R 4 are independently a linear or branched alkyl group having from 1 to about 22 carbon atoms
  • R 2 in each of the x (R O) and y (R 2 O) groups is independently ethylene or propylene
  • R 3 is hydrogen or methyl
  • the sum of x and y is an average number from about 2 to about 20.
  • R 1 is a linear or branched alkyl group having from about 8 to about 22 carbon atoms and R 4 is a linear or branched alkyl group having from 1 to about 22 carbon atoms
  • R 2 in each of the x (R 2 O) and y (R 2 O) groups is independently ethylene or propylene
  • R 3 is hydrogen or methyl
  • the sum of x and y is an average number from about 2 to about 20.
  • R 1 is a linear or branched alkyl group having from about 8 to about 22 carbon atoms and R 4 is a linear or branched alkyl group having from 1 to about 6 carbon atoms
  • R 2 in each of the x (R O) and y (R 2 O) groups is independently ethylene or propylene
  • R 3 is hydrogen or methyl
  • the sum of x and y is an average number from about 2 to about 15, or
  • R 1 and R 4 are independently a linear or branched alkyl group having from about 8 to about 22 carbon atoms
  • R 2 in each of the x (R 2 O) and y (R 2 O) groups is independently ethylene or propylene
  • R 3 is hydrogen or methyl
  • the sum of x and y is an average number from about 5 to about 15.
  • Preferred dialkoxylated quaternary ammonium surfactants include EthoquadTM C12 (a PEG 2 coco methyl ammonium chloride from Akzo Nobel), PEG 5 coco methyl ammonium chloride, PEG 5 tallow methyl ammonium chloride, PEG 5 ditallow ammonium bromide, and PEG 10 ditallow ammonium bromide.
  • EthoquadTM C12 a PEG 2 coco methyl ammonium chloride from Akzo Nobel
  • PEG 5 coco methyl ammonium chloride PEG 5 tallow methyl ammonium chloride
  • PEG 5 ditallow ammonium bromide PEG 5 ditallow ammonium bromide
  • PEG 10 ditallow ammonium bromide PEG 10 ditallow ammonium bromide.
  • R 1 and R 5 are independently hydrogen or hydrocarbyl or substituted hydrocarbyl having from 1 to about 30 carbon atoms
  • R 4 is hydrocarbyl or substituted hydrocarbyl having from 1 to about 30 carbon atoms
  • R 2 in each of the x (R 2 O) groups is independently C 2 -C 4 alkylene
  • R 3 is hydrogen, or a linear or branched alkyl group having from 1 to about 30 carbon atoms
  • x is an average number from 1 to about 60
  • X- is an agriculturally acceptable anion.
  • R 1 , R 4 , and R 5 hydrocarbyl groups are linear or branched alkyl, linear or branched alkenyl, linear or branched alkynyl, aryl, or aralkyl groups.
  • R ⁇ R 4 and R 5 are independently a linear or branched alkyl or linear or branched alkenyl group having from 1 to about 25 carbon atoms
  • R 2 in each of the x (R 2 O) groups is independently C 2 -C 4 alkylene
  • R 3 is hydrogen, methyl or ethyl
  • x is an average number from 1 to about 40.
  • R ⁇ R 4 and R 5 are independently a linear or branched alkyl group having from 1 to about 22 carbon atoms
  • R 2 in each of the x (R 2 O) groups is independently ethylene or propylene
  • R 3 is hydrogen or methyl
  • x is an average number from 1 to about 30.
  • R 1 is a linear or branched alkyl group having from about 8 to about 22 carbon atoms
  • R 2 in each of the x (R 2 O) groups is independently ethylene or propylene
  • R 3 is hydrogen or methyl
  • R 4 and R 5 are independently a linear or branched alkyl group having from 1 to about 22 carbon atoms
  • x is an average number from 1 to about 30.
  • R 1 is a linear or branched alkyl group having from about 8 to about 22 carbon atoms
  • R 2 in each of the x (R 2 O) groups is independently ethylene or propylene
  • R 3 is hydrogen or methyl
  • R 4 and R 5 are independently a linear or branched alkyl group having from 1 to about 6 carbon atoms
  • x is an average number from about 5 to about 25.
  • R 1 is a linear or branched alkyl group having from about 16 to about 22 carbon atoms
  • R 2 in each of the x (R 2 O) groups is independently ethylene or propylene
  • R 3 is hydrogen or methyl
  • R 4 and R 5 are independently a linear or branched alkyl group having from 1 to about 3 carbon atoms
  • x is an average number from about 5 to about 25.
  • Preferred monoalkoxylated quaternary ammonium surfactants include PEG 7 C 18 dimethyl ammonium chloride and PEG 22 C 18 dimethyl ammonium chloride, (e) a quaternary ammonium salt having the formula:
  • R 1 , R 3 and R 4 are independently hydrogen or hydrocarbyl or substituted hydrocarbyl having from 1 to about 30 carbon atoms
  • R 2 is hydrocarbyl or substituted hydrocarbyl having from 1 to about 30 carbon atoms
  • X- is an agriculturally acceptable anion.
  • preferred R 1 , R 2 , R 3 , and R 4 hydrocarbyl groups are linear or branched alkyl, linear or branched alkenyl, linear or branched alkynyl, aryl, or aralkyl groups.
  • R 1 is a linear or branched alkyl or linear or branched alkenyl group having from about 8 to about 30 carbon atoms
  • R 2 ', R 3 and R 4 are independently a linear or branched alkyl or linear or branched alkenyl group having from 1 to about 30 carbon atoms.
  • R 1 is a linear or branched alkyl or linear or branched alkenyl group having from about 8 to about 22 carbon atoms
  • R 2 ', R 3 and R 4 are independently a linear or branched alkyl or linear or branched alkenyl group having from 1 to about 6 carbon atoms.
  • R 1 is a linear or branched alkyl group having from about 8 to about 16 carbon atoms
  • R 2 ', R 3 and R 4 are independently a linear or branched alkyl group having from 1 to about 6 carbon atoms.
  • R 1 is a linear or branched alkyl group having from about 8 to about 14 carbon atoms
  • R 2t , R 3 and R 4 are methyl.
  • Preferred commercially available quaternary ammonium surfactants include ArquadTM C-50 (a dodecyl trimethyl ammonium chloride from Akzo Nobel) and ArquadTM T-50 (a tallow trimethyl ammonium chloride from Akzo Nobel).
  • R 1 is hydrocarbyl or substituted hydrocarbyl having from 1 to about 30 carbon atoms
  • R 2 is hydrocarbylene or substituted hydrocarbylene having from 2 to about 30 carbon atoms
  • R 3 and R 4 are independently hydrogen, hydrocarbyl or substituted hydrocarbyl having from 1 to about 30 carbon atoms, or -(R 5 O) x R 6 , R 5 in each of the x(R 5 -O) groups is independently C 2 -C 4 alkylene
  • R 6 is hydrogen, or a linear or branched alkyl group having from 1 to about 4 carbon atoms
  • x is an average number from 1 to about 50.
  • R 1 , R 2 , R 3 , and R 4 hydrocarbyl (hydrocarbylene) groups are linear or branched alkyl (alkylene), linear or branched alkenyl (alkenylene), linear or branched alkynyl (alkynylene), aryl (arylene), or aralkyl (aralkylene) groups.
  • R 1 is a linear or branched alkyl, linear or branched alkenyl, linear or branched alkynyl, aryl, or aralkyl group having from 8 to about 25 carbon atoms
  • R 2 is a linear or branched alkylene or alkenylene group having from 2 to about 30 carbon atoms
  • R 3 and R 4 are independently hydrogen, a linear or branched alkyl, linear or branched alkenyl, linear or branched alkynyl, aryl, or aralkyl group having from 1 to about 30 carbon atoms, or -(R 5 O) x R 6 , R 5 in each of the x (R 5 O) groups is independently C 2 -C 4 alkylene
  • R 6 is hydrogen, methyl or ethyl
  • x is an average number from 1 to about 30.
  • R 1 is a linear or branched alkyl or alkenyl group having from 8 to about 22 carbon atoms
  • R 2 is a linear or branched alkylene or alkenylene group having from 2 to about 6 carbon atoms
  • R 3 and R 4 are independently hydrogen, a linear or branched alkyl or alkenyl group having from 1 to about 6 carbon atoms, or -(R 5 O) x R 6 , R 5 in each of the x (R 5 O) groups is independently ethylene or propylene
  • R 6 is hydrogen or methyl
  • x is an average number from 1 to about 15.
  • R 1 is a linear or branched alkyl or alkenyl group having from 8 to about 18 carbon atoms
  • R 2 is ethylene or propylene
  • R 3 and R 4 are independently hydrogen, methyl, or -(R 5 O) x R 6
  • R 5 in each of the x (R 5 O) groups is independently ethylene or propylene
  • R 6 is hydrogen
  • x is an average number from 1 to about 5.
  • R 1 , R 3 , R 4 and R 5 are independently hydrogen, hydrocarbyl or substituted hydrocarbyl having from 1 to about 30 carbon atoms, or -(R 6 O) x R 7 ;
  • R 2 and R 8 are independently hydrocarbylene or substituted hydrocarbylene having from 2 to about 30 carbon atoms
  • R 6 in each of the x (R 6 O) and y (R 6 O) groups is independently C 2 - C 4 alkylene
  • R 7 is hydrogen, or a linear or branched alkyl group having from 1 to about 30 carbon atoms
  • x is an average number from 1 to about 30,
  • X is -O-, -N(R 6 )-, -C(O)-, -C(O)O-, -OC(O)-, -N(R 9 )C(O)-, -C(O)N(R 9 )-, -S-, -SO-, or -SO 2 -
  • y
  • R 9 is hydrogen or hydrocarbyl or substituted hydrocarbyl.
  • preferred R ⁇ R 2 , R 3 , R 4 , R 5 and R 9 hydrocarbyl (hydrocarbylene) groups are linear or branched alkyl (alkylene), linear or branched alkenyl (alkenylene), linear or branched alkynyl (alkynylene), aryl (arylene), or aralkyl (aralkylene) groups.
  • R 1 and R 4 are independently a linear or branched alkyl or linear or branched alkenyl group having from about 1 to about 22 carbon atoms
  • R 2 and R 8 are independently linear or branched alkylene groups having from about 2 to about 25 carbon atoms
  • R 3 and R 5 are each independently hydrogen or a linear or branched alkyl group having from 1 to about 6 carbon atoms and n, y and z are 0; or
  • R ⁇ R 2 , R 3 and R 4 are independently hydrogen or a linear or branched alkyl or alkenyl group having from about 1 to about 6 carbon atoms
  • R 2 is a linear or branched alkylene or alkenylene group having from about 8 to about 25 carbon atoms, and n, y and z are 0;
  • R 1 , R 2 , R 3 and R 4 are independently hydrogen or a linear or branched alkyl or alkenyl group having from about 1 to about 6 carbon atoms
  • R 1 and R 4 are independently a linear or branched alkyl or linear or branched alkenyl group having from about 4 to about 18 carbon atoms
  • R 2 is a linear or branched alkylene group having from about 2 to about 6 carbon atoms
  • R 3 and R 5 are each independently hydrogen or a linear or branched alkyl group having from 1 to about 6 carbon atoms
  • n, y and z are 0; or
  • R 1 , R 2 , R 3 and R 4 are independently hydrogen or a linear or branched alkyl group having from about
  • R 2 is a linear or branched alkylene group having from about 8 to about 25 carbon atoms, and y is 0; or R ⁇ R 2 , R 3 and R 4 are independently hydrogen or a linear or branched alkyl group having from about 1 to about 6 carbon atoms, R 2 is a linear or branched alkylene group having from about 1 to about 6 carbon atoms, R 6 in each of the y (R 6 O) groups is independently ethylene or propylene, y is an average number from 1 to about 10 and n and z is 0; or R 1 and R 3 are independently a linear or branched alkyl group having from about 8 to about 22 carbon atoms, R 2 is a linear or branched alkylene group having from about 2 to about 6 carbon atoms, and R 4 and R 5 are each independently hydrogen, a linear or branched alkyl group having from 1 to about 6 carbon atoms, or -(R 6 O) x R 7 ,
  • Preferred diamines include Gemini 14-2-14, Gemini 14-3-14, Gemini 10-2-10, Gemini 10-3-10, Gemini 10-4-10, and Gemini 16-2-16 (C 10 , C 14 or C 16 ethylene, propylene or butylene N-methyl diamines from Monsanto), EthoduomeensTM, and JeffamineTM EDR-148.
  • R 1 , R 2 and R 3 are independently hydrogen, hydrocarbyl or substituted hydrocarbyl, -(R 4 O) x R 5 , or -R 6 (OR 4 ) x OR 5 ;
  • R 4 in each of the x (R 4 O) groups is independently C 2 -C 4 alkylene
  • R 5 is hydrogen, or a linear or branched alkyl group having from 1 to about 30 carbon atoms
  • R 6 is hydrocarbylene or substituted hydrocarbylene having from 2 to about 6 carbon atoms
  • x in each of the x (R 4 O) groups is independently an average number from 1 to about 50, and the total number of carbon atoms in R 1 , R 2 and R 3 is at least 8.
  • R 1 , R 2 , R 3 , and R 6 hydrocarbyl (hydrocarbylene) groups are linear or branched alkyl (alkylene), linear or branched alkenyl (alkenylene), linear or branched alkynyl (alkynylene), aryl (arylene), or aralkyl (aralkylene) groups.
  • R 1 and R 2 are independently hydrogen, a linear or branched alkyl or linear or branched alkenyl group having from 1 to about 30 carbon atoms, or -(R 4 O) x R 5 ;
  • R 3 is a linear or branched alkyl or linear or branched alkenyl group having from about 8 to about 30 carbon atoms,
  • R 4 in each of the x (R 4 O) groups is independently C 2 -C 4 alkylene;
  • R 5 is hydrogen, methyl or ethyl, and x is an average number from 1 to about 30.
  • R 1 and R 2 are independently hydrogen, or a linear or branched alkyl group having from 1 to about 6 carbon atoms, and R 3 is a linear or branched alkyl group having from about 8 to about 22 carbon atoms; or R 1 and R 2 are independently -(R 4 O) x R 5 , R 3 is a linear or branched alkyl group having from about 8 to about 22 carbon atoms, R 4 in each of the x (R 4 O) groups is ethylene or propylene, R 5 is hydrogen or methyl, and x is an average number from 1 to about 10.
  • R 1 and R 2 are independently methyl, and R 3 is a linear or branched alkyl group having from about 8 to about 18 carbon atoms; or R 1 and R 2 are independently -(R 4 O) x R 5 , R 3 is a linear or branched alkyl group having from about 8 to about 18 carbon atoms, R 4 in each of the x (R 4 O) groups is ethylene or propylene, R 5 is hydrogen, and x is an average number from 1 to about 5.
  • amine oxide surfactants include Chemoxide L70. (i) a dialkoxylated amine having the formula:
  • R 1 is a hydrocarbyl or substituted hydrocarbyl having from about 6 to about 30 carbon atoms, or -R 4 SR 5 , R 4 and R 2 in each of the x (R 2 O) and the y (R 2 O) groups is independently C 2 -C 4 alkylene
  • R 3 is hydrogen, or a linear or branched alkyl group having from 1 to about 4 carbon atoms
  • R 5 is a linear or branched alkyl group having from about 4 to about 15 carbon atoms
  • x and y are independently an average number from 1 to about 40.
  • R 1 hydrocarbyl groups are linear or branched alkyl, linear or branched alkenyl, linear or branched alkynyl, aryl, or aralkyl groups.
  • R 1 is a linear or branched alkynyl, aryl, or aralkyl group having from about 8 to about 30 carbon atoms
  • R 2 in each of the x (R 2 O) and the y (R 2 O) groups is independently C 2 -C 4 alkylene
  • R 3 is hydrogen, methyl or ethyl
  • x and y are independently an average number from 1 to about 20.
  • R 1 is a linear or branched alkynyl, aryl, or aralkyl group having from about 8 to about 25 carbon atoms
  • R 2 in each of the x (R 2 O) and the y (R 2 O) groups is independently ethylene or propylene
  • R 3 is hydrogen or methyl
  • x and y are independently an average number from 1 to about 30.
  • R 1 is a linear or branched alkynyl, aryl, or aralkyl group having from about 8 to about 22, or about 12 to about 22, carbon atoms
  • R 2 in each of the x (R 2 O) and the y (R 2 O) groups is independently ethylene or propylene
  • R 3 is hydrogen or methyl
  • x and y are independently an average number from 1 to about 5.
  • dialkoxylated amines include, for example, TrymeenTM 6617 (from Cognis) and EthomeenTM C/12, C/15, C/20, C/25, T/12, T/15, T/20 and T/25 (from Akzo Nobel). and (j) an aminated alkoxylated alcohol having the formula:
  • R 1 , R 7 , R 8 , and R 9 are each independently hydrogen, hydrocarbyl or substituted hydrocarbyl having from 1 to about 30 carbon atoms, or -(R 11 ) s (R 3 O) v R 10 ;
  • X is -O-, -OC(O)-, -C(O)O-, -N(R 12 )C(O)-, -C(O)N(R 12 )-, -S-, -SO-, -SO 2 - or -N(R 9 )-;
  • R 3 in each of the n (R 3 O) groups and the v (R 3 O) groups is independently C 2 -C 4 alkylene;
  • R 10 is hydrogen, or a linear or branched alkyl group having from 1 to about 30 carbon atoms;
  • n is an average number from 1 to about 60;
  • v is an average number from 1 to about 50;
  • R 2 and R 11 are each independently hydrocarby
  • preferred R ⁇ R 2 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 11 and R 12 hydrocarbyl (hydrocarbylene) groups are linear or branched alkyl (alkylene), linear or branched alkenyl (alkenylene), linear or branched alkynyl (alkynylene), aryl (arylene), or aralkyl (aralkylene) groups.
  • a subclass of such cationic surfactants includes monoalkoxylated amines having the formula:
  • R 1 is hydrogen or hydrocarbyl or substituted hydrocarbyl having from 1 to about 30 carbon atoms
  • R 2 in each of the x (R 2 O) and y (R 2 O) groups is independently C 2 -C 4 alkylene
  • R 3 is hydrocarbylene or substituted hydrocarbylene having from 2 to about 30 carbon atoms
  • R 4 and R 5 are each independently hydrogen, hydrocarbyl or substituted hydrocarbyl having from 1 to about 30 carbon atoms, -(R 6 ) n -(R O) y R 7 , or R 4 and R 5 , together with the nitrogen atom to which they are attached, form a cyclic or heterocyclic ring
  • R 6 is hydrocarbylene or substituted hydrocarbylene having from 1 to about 30 carbon atoms
  • R 7 is hydrogen or a linear or branched alkyl group having 1 to about 4 carbon atoms, n is 0 or 1
  • x and y are 5 independently an average number from 1 to about 60.
  • R 1 , R 3 , R 4 , R 5 , and R 6 hydrocarbyl (hydrocarbylene) groups are linear or branched alkyl (alkylene), linear or branched alkenyl (alkenylene), linear or branched alkynyl (alkynylene), aryl (arylene), or aralkyl (aralkylene) groups.
  • R 1 is a linear or branched alkyl or linear or branched alkenyl group having from about 8 to about
  • R 2 in each of the x (R 2 O) groups is independently C 2 -C 4 alkylene
  • R 3 is a linear or branched alkylene group having from 2 to about 20 carbon atoms
  • R 4 and R 5 are each independently hydrogen or a linear or branched alkyl group having from 1 to about 6 carbon atoms
  • x is an average number from 1 to about 30. More preferably, R 1 is a linear or branched alkyl group having from about 12 to
  • R 2 in each of the x (R 2 O) groups is independently ethylene or propylene
  • R 3 is a linear or branched alkylene group having from 2 to about 6 carbon atoms
  • R 4 and R 5 are each independently hydrogen, methyl, or tris(hydroxymethyl)methyl
  • x is an average number from about 2 to about 30.
  • R 1 is a linear or branched alkyl group having from about 12 to 0 about 18 carbon atoms
  • R 2 in each of the x (R 2 O) groups is independently ethylene or propylene
  • R 3 is ethylene or propylene
  • R 4 and R 5 are each independently hydrogen, methyl or tris(hydroxymethyl)methyl
  • x is an average number from about 4 to about 20.
  • R 1 is a linear or branched alkyl group having from about 12 to about 18 carbon atoms
  • R 2 in each of the x (R 2 O) groups is 5 independently ethylene or propylene
  • R 3 is ethylene
  • R 4 and R 5 are methyl
  • x is an average number from about 4 to about 20.
  • Preferred monoalkoxylated amines include PEG 13 or 18 C 14 . 15 ether propylamines and PEG 7, 10, 15 or 20 C 16 . 18 ether propylamines (from Tomah) and PEG 13 or 18 C 14 . 15 ether dimethyl propylamines and PEG 10, 15 or 20 or 25 C 16 . 18 ether dimethyl propylamines (from Tomah) and 0 SurfonicTM AGM-550 from Huntsman.
  • Quaternary ammonium, sulfonium and sulfoxonium salts are also effective cationic surfactants in forming glyphosate concentrates and have the chemical structures:
  • R 1 , R 7 , R 8 , R 9 , R 10 and R 11 are independently hydrogen, hydrocarbyl or substituted hydrocarbyl having from 1 to about 30 carbon atoms, or -(R 13 ) s (R 3 O) v R 12 ;
  • X is -O-, -OC(O)-, -N(R 14 )C(O)-, -C(O)N(R 14 )-, -C(O)O-, or -S-;
  • R 3 in each of the n (R 3 O) groups and v (R 3 O) groups is independently C 2 -C 4 alkylene;
  • R 12 is hydrogen, or a linear or branched alkyl group having from 1 to about 30 carbon atoms;
  • n is an average number from 1 to about 60;
  • v is an average number from 1 to about 50;
  • R 2 and R 13 are each independently hydrocarbylene or substituted hydrocarbylene having from 1 to about 6 carbon atom
  • preferred R ⁇ R 2 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 13 , and R 14 hydrocarbyl (hydrocarbylene) groups are linear or branched alkyl (alkylene), linear or branched alkenyl (alkenylene), linear or branched alkynyl (alkynylene), aryl (arylene), or aralkyl (aralkylene) groups.
  • R 1 , R 4 , R 5 , R 6 , R 7 and R 8 are independently hydrogen or hydrocarbyl or substituted hydrocarbyl having from 1 to about 30 carbon atoms
  • R 2 in each of the m (R 2 O) and n (R 2 O) groups and R 9 are independently C 2 -C 4 alkylene
  • R 3 is hydrocarbylene or substituted hydrocarbylene having from about 2 to about 6 carbon atoms or -(R 2 O) p Rg-
  • m and n are individually an average number from 0 to about 50
  • p is an average number from 0 to about 60.
  • R ⁇ R 3 , R 4 , R 5 , R 6 , R 7 and R 8 hydrocarbyl (hydrocarbylene) groups are linear or branched alkyl (alkylene), linear or branched alkenyl (alkenylene), linear or branched alkynyl (alkynylene), aryl (arylene), or aralkyl (aralkylene) groups.
  • R 3 is hydrocarbylene having from about 2 to about 6 carbon atoms, and the remaining groups are as defined above.
  • Preferred nonionic surfactants for such glyphosate concentrates include alkoxylated alcohols having the formula:
  • R 1 is hydrocarbyl or substituted hydrocarbyl having from 1 to about 30 carbon atoms
  • R 2 in each of the x (R O) groups is independently C 2 -C 4 alkylene
  • R 3 is hydrogen, or a linear or branched alkyl group having from 1 to about 4 carbon atoms
  • x is an average number from 1 to about 60.
  • preferred R 1 hydrocarbyl groups are linear or branched alkyl, linear or branched alkenyl, linear or branched alkynyl, aryl, or aralkyl groups.
  • R 1 is a linear or branched alkyl or linear or branched alkenyl group having from about 8 to about 30 carbon atoms
  • R 2 in each of the x (R 2 O) groups is independently C 2 -C 4 alkylene
  • R 3 is hydrogen, methyl or ethyl
  • x is an average number from about 5 to about 50.
  • R 1 is a linear or branched alkyl group having from about 8 to about 25 carbon atoms
  • R 2 in each of the x (R 2 O) groups is independently ethylene or propylene
  • R 3 is hydrogen or methyl
  • x is an average number from about 8 to about 40.
  • R 1 is a linear or branched alkyl group having from about 12 to about 22 carbon atoms
  • R 2 in each of the x (R 2 O) groups is independently ethylene or propylene
  • R 3 is hydrogen or methyl
  • x is an average number from about 8 to about 30.
  • Preferred commercially available alkoxylated alcohols include ProcolTM LA-15 (from Protameen), BrijTM 35, BrijTM 76, BrijTM 78, BrijTM 97 and BrijTM 98 (from Sigma Chemical Co.), NeodolTM 25-12 (from Shell), HexotolTM CA-10, HexotolTM CA-20, HexotolTM CS-9, HexotolTM CS-15, HexotolTM CS-20, HexotolTM CS-25, HexotolTM CS-30, and PlurafacTM A38 (from BASF), ST- 8303 (from Cognis), and ArosurfTM 66 E20 (from Witco/Crompton).
  • nonionic surfactants for use in such glyphosate compositions or formulations include alkoxylated dialkylphenols having the formula:
  • R 1 and R 4 are independently hydrogen, or a linear or branched alkyl group having from 1 to about 30 carbon atoms and at least one of R 1 and R 4 is an alkyl group
  • R 2 in each of the x (R 2 O) groups is independently C 2 -C 4 alkylene
  • R 3 is hydrogen, or a linear or branched alkyl group having from 1 to about 4 carbon atoms
  • x is an average number from 1 to about 60.
  • R 1 and R 4 are independently linear or branched alkyl groups having from 8 to about 30 carbon atoms
  • R 2 in each of the x (R 2 O) groups is independently C 2 -C 4 alkylene
  • R 3 is hydrogen, methyl or ethyl
  • x is an average number from about 5 to about 50.
  • R 1 and R 4 are independently linear or branched alkyl groups having from about 8 to about 22 carbon atoms
  • R 2 in each of the x (R 2 O) groups is independently ethylene or propylene
  • R 3 is hydrogen or methyl
  • x is an average number from about 8 to about 40.
  • R 1 and R 4 are independently linear or branched alkyl groups having from about 8 to about 16 carbon atoms
  • R 2 in each of the x (R 2 O) groups is independently ethylene or propylene
  • R 3 is hydrogen or methyl
  • x is an average number from about 10 to about 30.
  • Preferred commercially available alkoxylated dialkylphenols include ethoxylated dinonyl phenols such as SurfonicTM DNP 100, SurfonicTM DNP 140, and SurfonicTM DNP 240 (from Huntsman).
  • Preferred anionic surfactants effective in forming glyphosate compositions or formulations may include saturated carboxylic acids such as butyric, caproic, caprylic, capric, lauric, palmitic, myristic or stearic acid, and unsaturated carboxylic acids such as palmitoleic, oleic, linoleic or linolenic acid.
  • Preferred carboxylic acids in at least some embodiments, may include palmitic, oleic or stearic acid.
  • Other preferred anionic surfactants in at least some embodiments, may include alkyl sulfates such as sodium lauryl sulfate, and alkyl alkoxylated phosphates having the formulae:
  • R 1 and R 3 are independently a linear or branched alkyl, linear or branched alkenyl, linear or branched alkynyl, aryl, or aralkyl group having from about 4 to about 30 carbon atoms;
  • R 2 in each of the m (R 2 O) and the n (R 2 O) groups is independently C 2 -C 4 alkylene; and m and n are independently from 1 to about 30; or
  • R 1 is a linear or branched alkyl, linear or branched alkenyl, linear or branched alkynyl, aryl, or aralkyl group having from about 8 to about 30 carbon atoms
  • R 2 in each of the m (R 2 O) groups is independently C 2 -C 4 alkylene
  • m is from 1 to about 30.
  • Representative alkyl alkoxylated phosphates include oleth-10 phosphate, oleth-20 phosphate and oleth-25 phosphate.
  • alkyl alkoxylated phosphates include those wherein, in (21 ), R 1 has about 10 to about 15 carbon atoms, R 2 is ethylene or propylene, and m is from about 1 to about 10, from about 2 to about 8, or about 4 to about 6.
  • R 1 has about 10 to about 15 carbon atoms
  • R 2 is ethylene or propylene
  • m is from about 1 to about 10, from about 2 to about 8, or about 4 to about 6.
  • exemplary surfactants that may be used in accordance with the present invention include the following species:
  • the weight ratio of glyphosate (a.e. basis) to surfactant may range from about 1 :10 to 10:1 or more (e.g., from about 1 :8 to 8:1 , from about 1 :6 to about 6:1 , from about 1 :4 to about 4:1 , from about 1 :3 to about 3:1 , or from about 1 :2 to about 2:1 ).
  • this ratio may range from about 1 :1 to about 10:1 (e.g., from about 1 :1 to about 10:1 , from about 2:1 to about 8:1 , or from about 3:1 to about 6:1 ), from about 1 :1 to about 15:1 , from about 1 :1 to about 20:1 , or more.
  • exemplary ratios include about 1 :10, about 1 :9.5, about 1 :9, about 1 :8.5, about 1 :8, about 1 :7.5, about 1 :7, about 1 :6.5, about 1 :6, about 1 :5.5, about 1 :5, about 1 :4.5, about 1 :4, about 1 :3.5, about 1 :3, about 12.5, about 1 :2, about 1 :1.5, about 1 :1 , about 1.5:1 , about 2:1 , about 2.5:1 , about 3:1 , about 3.5:1 , about 4:1 , about 4.5:1 , 5 about 5:1 , about 5.5:1 , about 6:1 , about 6.5:1 , about 7:1 , about 7.5:1 , about 8:1 , about 8.5:1 , about 9:1 , about 9.5:1 , about 10:1 , about 11 :1 , about 12:1 , about 13:1 , about 14:1 , about 15:1 , ,
  • the weight ratio of glyphosate (a.e. basis) to surfactant may range from about 10:1 to about 1 :5 (e.g., from about 8:1 to about 1 :4, from about 6:1 to about 1 :3, from about 4:1 to about 1 :2, or from about 2:1 to about 1 :1 ).
  • the surfactant concentration may be at least about 1 gram per liter (e.g., at least about 5, 10, 20, 30, 40, 50, 60, 70,
  • the surfactant concentration may range from about 1 to 283 grams per liter (e.g., 0 ranging for example from about 1 to about 275 grams per liter, from about 5 to about 250 grams per liter, from about 10 to about 100 grams per liter, from about 20 to about 80 grams per liter, or from about 40 to about 60 grams per liter).
  • the surfactant concentration may not be greater than 3.9 grams per liter (e.g., not greater than 3.8, 5 3.6, 3.4, 3.2, 3, 2.8, 2.6, 2.4, 2.2, 2, 1.8, 1.6, 1.4, 1.2, 1 or less), when the weight ratio (a.e. to a.e.) of glyphosate to pyridine analog (triclopyr, for example) is at least 3:1.
  • the surfactant concentration may not be greater than 6.6 grams per liter (e.g., not greater than 6.4, 6.2, 6, 5.8, 5.6, 5.4, 5.2, 5, 4.8, 4.6, 4.4, 4.2, 4, 3.8, etc.), when the weight ratio (a.e. to a.e.) of glyphosate to 0 pyridine analog (triclopyr, for example) is at least 5:1.
  • the surfactant concentration may not be greater than 9.3 grams per liter (e.g., not greater than 9.2, 9. 8.8, 8.6, 8.4, 8.2, 8, 7.8, 7.6, 7.4, 7.2, 7, 6.8, 6.6, 6.4, etc.), when the weight ratio (a.e. to a.e.) of glyphosate to pyridine analog (triclopyr, for example) is at least 7:1.
  • compositions of the present invention typically have a cloud point of at least about 50°C, or even about 60°C.
  • the aqueous concentrate and/or the ready- to-use composition of the present invention typically has a composition such that triclopyr (or more generally the pyridine analog) will not crystallize or precipitate when the bulk solution freezes or solidifies, and then thaws; stated another way, the herbicide compositions or formulations of the present invention have a composition wherein the pyridine analog, such as triclopyr, will not precipitate upon being cooled to a temperature of about 0°C, or even about -10°C.
  • compositions or formulations of the present invention may be introduced into the compositions or formulations of the present invention to improve certain properties thereof (e.g., solubility of the pyridine analog).
  • solubility of the pyridine analog e.g., solubility of the pyridine analog
  • a solubilizer also commonly referred to as a cloud point enhancer or stabilizer
  • Suitable solubilizers for use with the novel compositions or formulations of the present invention include, for example, cocoamine (Armeen C), dimethylcocoamine (Arquad DMCD), cocoammonium chloride (Arquad C), PEG 2 cocoamine (Ethomeen C12), a cocodiamine 3EO (Ethoduomeen CD/13), PEG 5 tallowamine (Ethomeen T15), and PEG 5 cocoamine (Ethomeen C15), all of which are manufactured by Akzo Nobel (California).
  • glyphosate salts e.g., potassium or isopropylamine
  • Suitable alkyl or aryl amine compounds may also contain 0 to about 5 EO groups.
  • Preferred alkylamine compounds include C 6 to C 12 alkylamines having 0 to 2 EO groups.
  • etheramine compounds having 4 to 12 carbons and 0 to about 5 EO groups also enhance the compatibility of such compositions or formulations.
  • the compounds which enhance the compatibility of such surfactants include amines or quaternary ammonium salts having the formula:
  • R 1 is linear or branched alkyl or aryl having from about 4 to about 16 carbon atoms
  • R 2 is hydrogen, methyl, ethyl, or -(CH 2 CH 2 O) x H
  • R 3 is hydrogen, methyl, ethyl, or -(CH 2 CH 2 O) y H wherein the sum of x and y is not more than about 5
  • R 4 is hydrogen or methyl
  • R 6 in each of the n (R 6 O) groups is independently C 2 -C 4 alkylene
  • R 5 is hydrocarbylene or substituted hydrocarbylene having from 2 to about 6 carbon atoms
  • A- is an agriculturally acceptable anion.
  • compositions of the present invention may further comprise one or more additional pesticides, such as for example, water- soluble herbicidal active ingredients, including without restriction water-soluble forms of acifluorfen, asulam, benazolin, bentazon, bialaphos, bispyribac, bromacil, bromoxynil, carfentrazone, chloramben, 2,4-D, 2,4-DB, dalapon, dicamba, dichlorprop, diclofop, difenzoquat, diquat, endothall, fenac, fenoxaprop, flamprop, fluazifop, fluoroglycofen, fomesafen, fosamine, glufosinate, haloxyfop, imazameth, imazamethabenz, imazamox, imazapic, imazapyr, imazaquin, imazethapyr, ioxynil, MCPA, MCPB, mecoprop
  • additional pesticides such
  • Another ingredient that can optionally be added to the glyphosate herbicidal compositions or formulations of the present invention to further improve the herbicidal effectiveness and related herbicidal properties is a di-carboxylic acid or salt of a di-carboxylic acid.
  • Suitable di-carboxylic acids that may be added to the herbicidal compositions or formulations comprising glyphosate or a salt or ester thereof and a surfactant as described herein include, for example, oxalic acid, malonic acid, succinic acid, glutaric acid, maleic acid, adipic acid, and fumaric acid, and combinations or mixtures thereof, with oxalic acid being preferred.
  • salts of the aforementioned di- carboxylic acids may be incorporated into the herbicidal formulations of the present invention to improve herbicidal performance.
  • Suitable salts include, for example, alkali metal salts such as potassium salts, alkanolamine salts and lower alkylamine salts.
  • Preferred salts include potassium oxalate, dipotassium oxalate, sodium oxalate, disodium oxalate, diammonium oxalate, diethanolamine oxalate, dimethylamine oxalate, alkanolamine salts of oxalic acid, and lower alkylamine salts of oxalic acid.
  • Formulations containing a di-carboxylic acid such as oxalic acid or a di- carboxylic acid salt such as potassium oxalate typically contain a sufficient amount of di-carboxylic acid/di-carboxylic acid salt to enhance the resulting efficacy of the herbicidal formulation.
  • the weight ratio of total surfactant to carboxylic acid/carboxylic acid salt may be, for example, from about 1 :1 to about 50:1 , about 5:1 to about 40:1 , or even about 5:1 to about 20:1. This ratio of total surfactant to carboxylic acid/carboxylic acid salt may significantly enhance the herbicidal performance of the resulting herbicidal formulation.
  • the di-carboxylic acid or salt thereof which can be added to herbicidal formulations of the present invention to improve efficacy are suitable for use with glyphosate, or salts thereof.
  • Suitable glyphosate salts include those listed above, such as for example the isopropylamine salt, the potassium salt, and the trimethylammonium salt.
  • compositions of the present invention are directed to a composition (e.g., a solid or liquid concentrate, or alternatively a ready-to-use composition) comprising glyphosate (or a derivative thereof), triclopyr or other pyridine analog (or a derivative thereof), a pelargonic acid (or nonanoic acid) or derivative thereof, and a surfactant, such as a linear alcohol ethoxylate.
  • a composition e.g., a solid or liquid concentrate, or alternatively a ready-to-use composition
  • glyphosate or a derivative thereof
  • triclopyr or other pyridine analog or a derivative thereof
  • a pelargonic acid or nonanoic acid
  • surfactant such as a linear alcohol ethoxylate.
  • Excipient ingredients other than the above-defined surfactant component can optionally be present in a composition of the invention, so long as the cloud point and non-crystallization properties of the composition remain in accordance with the invention.
  • additional excipient ingredients may include conventional formulation additives such as dyes, thickeners, crystallization inhibitors, antifreeze agents (e.g., glycols, such a ethylene glycol), foam moderating agents (e.g., AntifoamTM or Y-14088 AntifoamTM, both available from Crompton Corporation), antidrift agents, compatibilizing agents, antioxidants (e.g., ascorbic acid and sodium sulfite, in order for example to prevent the formation of a nitrosamine), other co- solvents (e.g., N-methylpyrrolidone, DMSO, DMF, propylene carbonate, or ethylene glycol), or some other agent added to lessen or overcome antagonism associated with hard water (e.g., ammonium sulfate
  • the herbicidal compositions of the invention can be prepared on site by the end-user shortly before application to the foliage of the vegetation to be killed or controlled by mixing in an aqueous solution (i) glyphosate or a herbicidal derivative thereof, (ii) a pyridine analog, such as triclopyr, or a derivative thereof, and (iii) a suitable surfactant.
  • aqueous solution glyphosate or a herbicidal derivative thereof,
  • a pyridine analog, such as triclopyr, or a derivative thereof a suitable surfactant.
  • Such compositions are typically referred to as "tank-mix" compositions.
  • herbicidal compositions of the present invention that are ready to be applied directly to foliage can be made with a glyphosate concentration as described elsewhere herein.
  • herbicidal compositions can be made with a triclopyr, or some other pyridine analog, at a concentration also as described elsewhere herein.
  • concentration of such compositions may be other than as described herein without departing from the scope of the present invention.
  • the herbicidal compositions of the invention may be provided to the end-user already formulated, either at the desired dilution for application (i.e., "ready-to-use” compositions) or requiring dilution, dispersion, or dissolution in water by the end-user (i.e., "concentrate” compositions, wherein the glyphosate concentration is at least about 50 grams (a.e.) per liter).
  • concentrates can be liquids or particulate solids.
  • the particulate solids, or dry formulations, of the present invention it is to be noted that these may be in the form of powders, pellets, tablets or granules. These dry formulations are typically dispersed or dissolved into water prior to use.
  • Dry water-soluble or water-dispersable formulations of the present invention typically comprise the same ratios of glyphosate to triclopyr (G:T), or more generally the same ratios of glyphosate to pyridine analog, and glyphosate to surfactant (G:S), as described elsewhere herein.
  • G:T triclopyr
  • G:S glyphosate to surfactant
  • dry formulations of the present invention the glyphosate itself may provide the support for other formulation constituents, or there may be additional inert ingredients which provide such support.
  • an inert support ingredient that may be used in accordance with the present invention is ammonium sulfate.
  • dry formulations of the present invention comprise from about 0.5% to about 5% (by weight) water. It is preferred that the dry formulations of the present invention contain less than about 1 % (by weight) water. Additionally, it is preferred for at least some embodiments that the particulate solid exhibits a dissolution rate of not more than about 5 minutes, about 4 minutes, about 3 minutes, about 2 minutes, or even about 1 minute.
  • Dry, water soluble or water dispersable formulations in accordance with the present invention can be produced by any process known in the art, including spray drying, fluid-bed agglomeration, pan granulation, or extrusion.
  • glyphosate may be present as a salt, or as an acid.
  • Formulations containing glyphosate acid may optionally contain an acid acceptor such as an ammonium or alkali metal carbonate or bicarbonate, ammonium dihydrogen phosphate or the like so that upon dissolution or dispersion in water by the user a water soluble salt of glyphosate is produced.
  • liquid concentrate formulations having an aqueous phase wherein glyphosate is present predominantly in the form of a salt, and a non-aqueous phase optionally containing a second herbicidal active ingredient that is relatively water-insoluble.
  • Such formulations illustratively include emulsions (including macro- and microemulsions, water-in-oil, oil-in-water and water- in-oil-in-water types), suspensions and suspoemulsions.
  • the non-aqueous phase can optionally comprise a microencapsulated component, for example a microencapsulated herbicide.
  • concentration of glyphosate a.e.
  • aqueous concentrate formulations include acetochlor, aclonifen, alachlor, ametryn, amidosulfuron, anilofos, atrazine, azafenidin, azimsulfuron, benfluralin, benfuresate, bensulfuron-methyl, bensulide, benzofenap, bifenox, bromobutide, bromofenoxim, butachlor, butamifos, butralin, butroxydim, butylate, cafenstrole, carbetamide, carfentrazone-ethyl, chlomethoxyfen, chlorbromuron, chloridazon, chlorimuron-ethyl, chlornitrofen, chlorotoluron, chlorpropham, chlorsulfuron, chlorthal-dimethyl
  • herbicidal spray compositions of the present invention are applied as aqueous solutions or dispersions, whether they result from the further dilution of the liquid concentrate or the addition of water to the particulate solid concentrate.
  • aqueous as used herein, is not intended to exclude the presence of some small amount of nonaqueous solvent, so long as the predominant solvent present, other than for example the glycol or glycol ester component of the surfactant composition, is water.
  • the present invention is additionally directed to a method of for killing or controlling weeds or unwanted vegetation which comprises the steps of diluting a liquid concentrate in a convenient amount of water to form a tank mix and applying a herbicidally effective amount of the tank mix to the foliage of the weeds or unwanted vegetation.
  • a method of for killing or controlling weeds or unwanted vegetation comprises the steps of diluting a liquid concentrate in a convenient amount of water to form a tank mix and applying a herbicidally effective amount of the tank mix to the foliage of the weeds or unwanted vegetation.
  • the herbicidal composition of the present invention is applied to plants at a rate sufficient to give the desired biological effects: control of plant growth and early visual symptoms of treatment.
  • the amount of glyphosate and triclopyr, or other pyridine analog, applied to plants in combination generally provides a herbicidally- effective amount of the herbicides.
  • the amount of glyphosate and triclopyr, or other pyridine analogy, applied to plants further is sufficient to provide early visual symptoms of plant treatment without significantly reducing the desired biological effect of the glyphosate.
  • These application rates are usually expressed as amount of glyphosate per unit area treated, e.g. grams per hectare (g/ha).
  • compositions Typically, the amount of the composition applied per unit area to give 85% control of a plant species as measured by growth reduction or mortality is often used to define a commercially effective rate.
  • Early visual symptoms of treatment typically appear no later than about 4 days after treatment, preferably no later than about 3 days after treatment, more preferably no later than about 2 days after treatment, and still more preferably no later than about 1 day after treatment.
  • the herbicidal spray compositions included in the present invention can be applied to the foliage of the plants to be treated through any of the appropriate methods that are well known to those having skill in the art. However, in one embodiment, the herbicidal composition is applied using means other than a helicopter; stated another way, in at least some embodiments the present invention is directed to methods wherein the herbicidal composition is applied using non-aerial means (i.e., ground application techniques, such as a hand sprayer, rope-wick, etc.) or using a fixed-wing aircraft.
  • non-aerial means i.e., ground application techniques, such as a hand sprayer, rope-wick, etc.
  • Particularly important annual dicotyledonous plant species for control of which a composition of the invention can be used are exemplified without limitation by velvetleaf (Abutilon theophrasti), pigweed (Amaranthus spp.), buttonweed (Borreria spp.), oilseed rape, canola, indian mustard, etc. (Brassica spp.), commelina (Commelina spp.), filaree (Erodium spp.), sunflower (Helianthus spp.), morningglory (Ipomoea spp.), kochia (Kochia scoparia), mallow (Malva spp.), wild buckwheat, smartweed, etc.
  • Particularly important annual monocotyledonous plant species for control of which a composition of the invention can be used are exemplified without limitation by wild oat (Avena fatua), carpetgrass (Axonopus spp.), downy brome (Bromus tectorum), crabgrass (Digitaria spp.), barnyardgrass (Echinochloa crus-galli), goosegrass (Eleusine indica), annual ryegrass (Lolium multiflorum), rice (Oryza sativa), ottochloa (Ottochloa nodosa), bahiagrass (Paspalum notatum), canarygrass (Phalaris spp.), foxtail (Setaria spp.), wheat (Triticum aestivum) and corn (Zea mays).
  • Particularly important perennial dicotyledonous plant species for control of which a composition of the invention can be used are exemplified without limitation by mugwort (Artemisia spp.), milkweed (Asclepias spp.), Canada thistle (Cirsium arvense), field bindweed (Convolvulus arvensis) and kudzu (Pueraria spp.).
  • Particularly important perennial monocotyledonous plant species for control of which a composition of the invention can be used are exemplified without limitation by brachiaria (Brachiaria spp.), bermudagrass (Cynodon dactylon), yellow nutsedge (Cyperus esculentus), purple nutsedge (C.
  • compositions of the invention can be used are exemplified without limitation by horsetail (Equisetum spp.), bracken (Pteridium aquilinum), blackberry (Rubus spp.) and gorse (Ulex europaeus).
  • the user can mix one or more adjuvants with a composition of the invention and the water of dilution when preparing the application composition.
  • Such adjuvants can include additional surfactant and/or an inorganic salt such as ammonium sulfate with the aim of further enhancing herbicidal efficacy.
  • additional surfactant and/or an inorganic salt such as ammonium sulfate with the aim of further enhancing herbicidal efficacy.
  • an inorganic salt such as ammonium sulfate
  • a herbicidal method of use of the present invention gives acceptable efficacy in the absence of such adjuvants.
  • the composition following dilution in water, is applied to foliage of crop plants genetically transformed or selected to tolerate glyphosate, and simultaneously to foliage of weeds or undesired plants growing in close proximity to such crop plants.
  • Crop plants genetically transformed or selected to tolerate glyphosate include those whose seeds are sold by Monsanto Company or under license from Monsanto Company bearing the Roundup Ready® trademark. These include, without restriction, varieties of cotton, soybean, canola, sugar beet, wheat and corn.
  • Plant treatment compositions can be prepared simply by diluting a concentrate composition of the invention in water. Application of plant treatment compositions to foliage is preferably accomplished by spraying, using any conventional means for spraying liquids, such as spray nozzles, atomizers or the like.
  • Compositions of the invention can be used in precision farming techniques, in which apparatus is employed to vary the amount of pesticide applied to different parts of a field, depending on variables such as the particular plant species present, soil composition, etc.
  • a global positioning system operated with the spraying apparatus can be used to apply the desired amount of the composition to different parts of a field.
  • hydrocarbon and “hydrocarbyl” as used herein describe organic compounds or radicals consisting exclusively of the elements carbon and hydrogen. These moieties include alkyl, alkenyl, alkynyl, and aryl moieties. These moieties also include alkyl, alkenyl, alkynyl, and aryl moieties substituted with other aliphatic or cyclic hydrocarbon groups, such as alkaryl, alkenaryl and alkynaryl. Unless otherwise indicated, these moieties preferably comprise 1 to 30 carbon atoms.
  • hydrocarbylene as used herein describes radicals joined at two ends thereof to other radicals in an organic compound, and which consist exclusively of the elements carbon and hydrogen.
  • moieties include alkylene, alkenylene, alkynylene, and arylene moieties. These moieties also include alkyl, alkenyl, alkynyl, and aryl moieties substituted with other aliphatic or cyclic hydrocarbon groups, such as alkaryl, alkenaryl and alkynaryl. Unless otherwise indicated, these moieties preferably comprise 1 to 30 carbon atoms.
  • substituted hydrocarbyl moieties described herein are hydrocarbyl moieties which are substituted with at least one atom other than carbon, including moieties in which a carbon chain atom is substituted with a hetero atom such as nitrogen, oxygen, silicon, phosphorous, boron, sulfur, or a halogen atom.
  • substituents include halogen, heterocyclo, alkoxy, alkenoxy, alkynoxy, aryloxy, hydroxy, protected hydroxy, ketal, acyl, acyloxy, nitro, amino, amido, cyano, thiol, acetal, sulfoxide, ester, thioester, ether, thioether, hydroxyalkyl, urea, guanidine, amidine, phosphate, amine oxide, and quaternary ammonium salt.
  • substituted hydrocarbylene moieties described herein are hydrocarbylene moieties which are substituted with at least one atom other than carbon, including moieties in which a carbon chain atom is substituted with a hetero atom such as nitrogen, oxygen, silicon, phosphorous, boron, sulfur, or a halogen atom.
  • substituents include halogen, heterocyclo, alkoxy, alkenoxy, alkynoxy, aryloxy, hydroxy, protected hydroxy, ketal, acyl, acyloxy, nitro, amino, amido, cyano, thiol, acetal, sulfoxide, ester, thioester, ether, thioether, hydroxyalkyl, urea, guanidine, amidine, phosphate, amine oxide, and quaternary ammonium salt.
  • the alkyl groups described herein are preferably lower alkyl containing from one to 18 carbon atoms in the principal chain and up to 30 carbon atoms. They may be straight or branched chain or cyclic and include methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, hexyl, 2-ethylhexyl, and the like.
  • the alkenyl groups described herein are preferably lower alkenyl containing from two to 18 carbon atoms in the principal chain and up to 30 carbon atoms.
  • alkynyl groups described herein are preferably lower alkynyl containing from two to 18 carbon atoms in the principal chain and up to 30 carbon atoms. They may be straight or branched chain and include ethynyl, propynyl, butynyl, isobutynyl, hexynyl, and the like.
  • aryl as used herein alone or as part of another group denote optionally substituted homocyclic aromatic groups, preferably monocyclic or bicyclic groups containing from 6 to 12 carbons in the ring portion, such as phenyl, biphenyl, naphthyl, substituted phenyl, substituted biphenyl or substituted naphthyl. Phenyl and substituted phenyl are the more preferred aryl.
  • aralkyl denotes a group containing both alkyl and aryl structures such as benzyl.
  • the alkyl, alkenyl, alkynyl, aryl and aralkyl groups can be substituted with at least one atom other than carbon, including moieties in which a carbon chain atom is substituted with a hetero atom such as nitrogen, oxygen, silicon, phosphorous, boron, sulfur, or a halogen atom.
  • substituents include hydroxy, nitro, amino, amido, nitro, cyano, sulfoxide, thiol, thioester, thioether, ester and ether, or any other substituent which can increase the compatibility of the surfactant and/or its efficacy enhancement in the glyphosate formulation without adversely affecting the storage stability of the formulation.
  • halogen or halo as used herein alone or as part of another group refer to chlorine, bromine, fluorine, and iodine. Fluorine substituents are often preferred in surfactant compounds.
  • hydroxyalkyl includes alkyl groups substituted with at least one hydroxy group, and includes bis(hydroxyalkyl)alkyl, tris(hydroxyalkyl)alkyl and poly(hydroxyalkyl)alkyl groups.
  • Preferred hydroxyalkyl groups include hydroxymethyl (-CH 2 OH), and hydroxyethyl (-C 2 H 4 OH), bis(hydroxymethyl)methyl (-CH(CH 2 OH) 2 ), and tris(hydroxymethyl)methyl (-C(CH 2 OH) 3 ).
  • cyclic as used herein alone or as part of another group denotes a group having at least one closed ring, and includes alicyclic, aromatic (arene) and heterocyclic groups.
  • heterocyclo or “heterocyclic” as used herein alone or as part of another group denote optionally substituted, fully saturated or unsaturated, monocyclic or bicyclic, aromatic or nonaromatic groups having at least one heteroatom in at least one ring, and preferably 5 or 6 atoms in each ring.
  • the heterocyclo group preferably has 1 or 2 oxygen atoms, 1 or 2 sulfur atoms, and/or 1 to 4 nitrogen atoms in the ring, and may be bonded to the remainder of the molecule through a carbon or heteroatom.
  • heterocyclo include heteroaromatics such as furyl, thienyl, pyridyl, oxazolyl, pyrrolyl, indolyl, quinolinyl, or isoquinolinyl and the like, and non-aromatic heterocyclics such as tetrahydrofuryl, tetrahydrothienyl, piperidinyl, pyrrolidino, etc.
  • substituents include one or more of the following groups: hydrocarbyl, substituted hydrocarbyl, keto, hydroxy, protected hydroxy, acyl, acyloxy, alkoxy, alkenoxy, alkynoxy, aryloxy, halogen, amido, amino, nitro, cyano, thiol, thioester, thioether, ketal, acetal, ester and ether.
  • heteromatic as used herein alone or as part of another group denote optionally substituted aromatic groups having at least one heteroatom in at least one ring, and preferably 5 or 6 atoms in each ring.
  • the heteroaromatic group preferably has 1 or 2 oxygen atoms, 1 or 2 sulfur atoms, and/or 1 to 4 nitrogen atoms in the ring, and may be bonded to the remainder of the molecule through a carbon or heteroatom.
  • exemplary heteroaromatics include furyl, thienyl, pyridyl, oxazolyl, pyrrolyl, indolyl, quinolinyl, or isoquinolinyl and the like.
  • substituents include one or more of the following groups: hydrocarbyl, substituted hydrocarbyl, keto, hydroxy, protected hydroxy, acyl, acyloxy, alkoxy, alkenoxy, alkynoxy, aryloxy, halogen, amido, amino, nitro, cyano, thiol, thioether, thioester, ketal, acetal, ester and ether.
  • acyl denotes the moiety formed by removal of the hydroxyl group from the group -COOH of an organic carboxylic acid, e.g., RC(O)-, wherein R is R ⁇ R 1 O-, R 1 R 2 N-, or R 1 S-, R 1 is hydrocarbyl, heterosubstituted hydrocarbyl, or heterocyclo and R 2 is hydrogen, hydrocarbyl or substituted hydrocarbyl.
  • acyloxy denotes an acyl group as described above bonded through an oxygen linkage (-O-), e.g., RC(O)O- wherein R is as defined in connection with the term "acyl.”
  • pesticide includes chemicals and microbial agents used as active ingredients of products for control of crop and lawn pests and diseases, animal ectoparasites, and other pests in public health.
  • the term also includes plant growth regulators, pest repellants, synergists, herbicide safeners (which reduce the phytotoxicity of herbicides to crop plants) and preservatives, the delivery of which to the target may expose dermal and especially ocular tissue to the pesticide. Such exposure can arise by drift of the pesticide from the delivery means to the person performing the application of the pesticide or being present in the vicinity of an application.
  • Herbicidal effectiveness refers to any observable measure of control of plant growth, which can include one or more of the actions of (1 ) killing, (2) inhibiting growth, reproduction or proliferation, and (3) removing, destroying, or otherwise diminishing the occurrence and activity of plants.
  • the herbicidal effectiveness data set forth herein report "control” as a percentage following a standard procedure in the art which reflects a visual assessment of plant mortality and growth reduction by comparison with untreated plants, made by technicians specially trained to make and record such observations. In all cases, a single technician makes all assessments of percent control within any one experiment or trial. Such measurements are relied upon and regularly reported by Monsanto Company in the course of its herbicide business.
  • Aqueous herbicide formulations were generated from commercially available glyphosate isopropylamine, triclopyr triethylamine and various surfactants in the ratios indicated in Tables 1.1 and 1.2.
  • a Glyphosate and triclopyr are expressed as the acid equivalent load (g ae/L).
  • the densities of the concentrate formulations are in the range 1.06 to 1.17 g/ml.
  • the ready-to-use formulation has a density of approx. 1.004g/ml.
  • the surfactant load is expressed as the weight/volume %, i.e. g/100ml.
  • the glyphosate/surfactant w/w ratio i.e., g ae/g surfactant per kg of formulation.
  • a Glyphosate load expressed as the weight of a standard (62% ai glyphosate) used per 1000g.
  • the densities of the concentrate formulations are in the range 1.06 to 1.17 g/ml.
  • the ready-to-use formulation has a density of approx. 1.004g/ml.
  • Triclopyr load expressed as the weight of a standard (44.3% ai triclopyr) used per 1000g.
  • the densities of the concentrate formulations are in the range 1.06 to 1.17 g/ml.
  • the ready-to-use formulation has a density of approx. 1.004g/ml.
  • the glyphosate/triclopyr w/w ratio is given in terms of the %ai/%ai.
  • the surfactant is expressed as the w/w% i.e., weight of surfactant standard per 100g.
  • FS1 surfactant composition is a mixture of tallowamines and phosphate esters, as described in U.S. Patent No. 5,703,015.
  • FS2 surfactant composition is a mixture of tallowamines and phosphate esters, as described in U.S. Patent No. 5,703,015.
  • FS3 surfactant composition is a mixture of a tallowamine ethoxylate with other surfactants.
  • FS4 is a Cocoamine 5EO.
  • FS5 is a Cocoamine 5EO.
  • the plants were maintained for the duration of the test in the greenhouse where they received a minimum of 14 hours of light per day. If natural light was insufficient to achieve the daily requirement, artificial light with an intensity of approximately 475 microeinsteins was used to make up the difference. Exposure temperatures were not precisely controlled but averaged about 27 °C during the day and about 21 °C during the night. Plants were sub-irrigated throughout the test to ensure adequate soil moisture levels. Pots were assigned to different treatments in a randomized experimental design with 6 replications. A set of pots was left untreated as a reference against which effects of the treatments could later be evaluated.
  • glyphosate compositions were made by spraying with a track sprayer fitted with a flateven 8008E nozzle calibrated to deliver a spray volume of 1348 liters per hectare (l/ha) at a pressure of 165 kilopascals (kPa). After treatment, pots were returned to the greenhouse until ready for evaluation. Treatments were made using dilute aqueous compositions.
  • F5M RTU is constructed as 17o glyphosate, isopropylamine salt and 0.10% triclopyr, triethylamine salt
  • F3M concentration formulation is constructed as 18% a.i. glyphosate and 2% a.i. triclopyr.
  • the brush tests were conducted on preexisting brush infestations typically located along and within fence and tree lines during June through August. All brush species were well-established and exhibiting complete foliation of leaf tissue at the time of treatment.
  • Brush control ratings were evaluated at 1 , 3, 21 and 90 days after treatment (DAT). Visual assessment of formulation efficacy was assessed on a 0 to 100% scale based on brush control (chorosis, necrosis and kill) compared to the untreated plots. Values close to 0% indicate no visual presence of brush damage by a formulation, while values approaching 1007o indicate complete kill of a brush species compared to untreated plots. In addition, values greater than 807o control indicate that a product is supplying the industry standard commercially acceptable weed/brush control.
  • F5M and F3M provided commercial control of tough to control brush. At 90 DAT brush control for all species tested ranged between 90 and 100% control (Tables 4.2.1 through 4.3.4). F5M and F3M tested at various regions and brush species will deliver effective weed control of unwanted vegetation up to 90DAT.
  • Untreated Check displayed some natural yellowing due to senescence, or aging.

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RU2413414C2 (ru) 2006-02-15 2011-03-10 Дау Агросайенсиз Ллс Композиция бутоксиэтилового эфира триклопира, не содержащая растворитель
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EP2712503A3 (de) 2016-03-23
NZ543037A (en) 2009-10-30
AU2004232335C9 (en) 2013-06-27
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AU2004232335A1 (en) 2004-11-04
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AU2004232335B2 (en) 2010-12-23
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