WO2011133482A1 - Aqueous herbicidal concentrates of auxinic carboxylic acids with reduced eye irritancy - Google Patents
Aqueous herbicidal concentrates of auxinic carboxylic acids with reduced eye irritancy Download PDFInfo
- Publication number
- WO2011133482A1 WO2011133482A1 PCT/US2011/032940 US2011032940W WO2011133482A1 WO 2011133482 A1 WO2011133482 A1 WO 2011133482A1 US 2011032940 W US2011032940 W US 2011032940W WO 2011133482 A1 WO2011133482 A1 WO 2011133482A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- auxinic
- choline
- ammonium
- salts
- carboxylic acids
- Prior art date
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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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/12—Quaternary ammonium compounds
Definitions
- This invention concerns the use of choline salts to reduce eye irritancy of aqueous herbicidal concentrates of commonly used ammonium salts of auxinic carboxylic acids derived from mono-, di- or trialkylamines.
- Aqueous concentrate formulations of pesticidal and plant growth modifying chemicals are widely used in agricultural, industrial, recreational and residential areas worldwide.
- the active ingredients of such concentrates are frequently carboxylic acids, more particularly their salts.
- An aqueous concentrate is essentially a solution of the active ingredient in water at relatively high concentration, intended for dilution in water prior to application by spraying or other means.
- the aqueous concentrate is diluted with 10 to 100 times its own volume of water prior to application.
- herbicidal carboxylic acids such as, for example, the phenoxycarboxylic acids like 2,4-D, 2,4-DB, MCPA, MCPB, mecoprop and clomeprop, the benzoic acids like dicamba and chloramben, the picolinic acids like aminopyralid, picloram and clopyralid, the pyridinyloxyacetic acids like triclopyr and fluroxypyr, and the quinolinecarboxylic acids like quinclorac and quinmerac are relatively insoluble in water in the acid form. Therefore, these herbicides are in many instances formulated as aqueous concentrates of water soluble salts.
- Commonly used salts of these herbicidal carboxylic acids used for preparing aqueous herbicide concentrates include, for example, ammonium, z ' so-propyl ammonium, dimethyl ammonium, triethyl ammonium, monoethanol ammonium, diethanol ammonium, triethanol ammonium, triisopropanol ammonium and the like, which are collectively referred herein as the ammonium salts.
- ammonium salts of herbicidal carboxylic acids to prepare aqueous herbicide concentrates is that they can be irritating if accidentally splashed or otherwise injected into the eye of anyone handling such a formulation. This property may lead to restrictive labeling of the products that limits their usefulness in certain markets, even where the active ingredient itself provides no such hazard.
- Choline is an essential nutrient for mammals, necessary for optimal health based on the Dietary Reference Intakes recommended by the National Academy of Sciences. Choline generally refers to the various quaternary ammonium salts containing the N,N,N-trimethyl- ethanolammonium cation and a counterion X such as, for example, chloride (choline chloride), hydroxide (choline hydroxide) or tartrate (choline tartrate).
- a counterion X such as, for example, chloride (choline chloride), hydroxide (choline hydroxide) or tartrate (choline tartrate).
- Choline hydroxide can be mixed with 2,4-D in water and readily forms the choline salt of 2,4-D which has the structure
- aqueous concentrates of choline salts of herbicidal auxinic carboxylic acids are less irritating to eyes than are the commonly used ammonium salts of such herbicidal auxinic carboxylic acids.
- These choline salts have herbicidal activity on an acid equivalent basis comparable to the commercially used carboxylic acid herbicide ammonium salts, such as z ' so-propyl ammonium, dimethyl ammonium, triethyl ammonium, monoethanol ammonium, diethanol ammonium, triethanol ammonium, triisopropanol ammonium salts and the like, but with reduced eye irritation.
- the choline salts can be conveniently formulated as aqueous concentrates.
- the present invention concerns a method to reduce the eye irritancy of aqueous herbicidal concentrates of commonly used ammonium salts of auxinic carboxylic acids derived from mono-, di- or trialkylamines which comprises using the ⁇ , ⁇ , ⁇ - trimethylethanolammonium cation as the ammonium salt of the auxinic carboxylic acid.
- Another aspect of the present invention concerns a mixture of one or more organophosphorous acid herbicide salts and the choline salts of the herbicidal auxinic carboxylic acids which provide an aqueous herbicide concentrate mixture of reduced eye irritancy.
- Another aspect of the present invention concerns a method of improving the solubility in water of ammonium salts of auxinic herbicides which comprises using the ⁇ , ⁇ , ⁇ - trimethylethanolammonium cation as the ammonium salt of the auxinic herbicide.
- Herbicidal auxinic carboxylic acids are carboxylic acid herbicides with the same mode of action as indoleacetic acid and is meant to include benzoic acid herbicides such as chloramben, dicamba, 2,3,6-TBA and tricamba; pyridine carboxylic acid herbicides such as aminopyralid, clopyralid and picloram; pyridinyloxy acetic acid herbicides such as triclopyr and fluroxypyr quinolinecarboxylic acid herbicides such as quinclorac and quinmerac;
- phenoxyacetic acid herbicides such as 4-CPA, 2,4-D, 3,4-DA and MCPA; phenoxybutyric herbicides such as 4-CPB, 2,4-DB, 3,4-DB and MCPB; phenoxypropionic herbicides such as cloprop, 4-CPP, dichlorprop, 3,4-DP, fenoprop, mecoprop and mecoprop-P.
- Preferred herbicidal auxinic carboxylic acids are 2,4-D, triclopyr, aminopyralid, clopyralid, fluroxypyr, picloram and dicamba.
- Choline hydroxide refers to the compound of the formula
- the present invention concerns aqueous concentrates comprised of one or more herbicidal auxinic carboxylic acid choline salts that have reduced eye irritancy compared to the commonly used aqueous concentrates of ammonium salts of herbicidal auxinic carboxylic acids.
- the choline salts have herbicidal activity on an acid equivalent basis comparable to the commercially used carboxylic acid herbicide ammonium salts, but with reduced eye irritation.
- the choline salts can be conveniently formulated as aqueous concentrates.
- the compounds of the present invention can be conveniently prepared by reaction of the herbicidal auxinic carboxylic acid with enough choline hydroxide to fully neutralize the herbicidal auxinic carboxylic acid.
- the herbicidal auxinic carboxylic acid is mixed with the choline hydroxide in water, optionally with the aid of a co-solvent, to provide the desired aqueous concentrate.
- Another aspect of the present invention concerns a mixture of one or more organophosphorous acid herbicide salts and the herbicidal auxinic carboxylic acid choline salts to provide aqueous herbicide concentrates of reduced eye irritancy.
- organophosphorous acid herbicides may comprise glufosinate and glyphosate in their commonly used salt forms selected from, for example, ammonium, isopropyl ammonium, dimethyl ammonium, triethyl ammonium, trimethylsulfonium, sodium, potassium and the like. These aqueous concentrate mixtures exhibit reduced eye irritancy compared to mixtures containing herbicidal auxinic carboxylic acid ammonium salts.
- Another aspect of the present invention concerns a method of improving the solubility in water of ammonium salts of auxinic herbicides which comprises using the ⁇ , ⁇ , ⁇ - trimethylethanolammonium cation (choline) as the ammonium salt of the auxinic herbicide.
- choline ⁇ , ⁇ , ⁇ - trimethylethanolammonium cation
- the triclopyr choline salt has significantly higher solubility in water than any known triclopyr salt even at temperatures as low as - 10°C.
- the solubility in water of the triclopyr choline salt is greater than the solubility in water of the commercially used triclopyr triethylammonium salt on an acid equivalent or an active ingredient basis.
- the unexpected high water solubility of the triclopyr choline salt allows the production of higher concentration formulations.
- High strength formulations are desirable for a variety of economic and environmental reasons. For example, it is desirable to provide a high strength formulation to reduce shipping and handling costs and to reduce the amount of packaging that must be disposed.
- the aqueous concentrates of the present invention can generally be employed to control undesirable vegetation in many crops that have been made tolerant to or resistant to them or to other herbicides by genetic manipulation or by mutation and selection. Many glyphosate and glufosinate tolerant crops can be treated as well, alone or in combination with these compounds. Some crops (e.g. corn, soybean and cotton) have been made tolerant to auxinic herbicides such as 2,4-dichlorophenoxyacetic acid. These active ingredients may be used to treat such resistant crops or other auxin tolerant crops.
- aqueous concentrates While it is possible to utilize the aqueous concentrates directly as herbicides, it is preferable to use them in mixtures containing a herbicidally effective amount of the aqueous concentrates along with at least one agriculturally acceptable adjuvant or carrier.
- Suitable adjuvants or carriers should not be phytotoxic to valuable crops, particularly at the concentrations employed in applying the compositions for selective weed control in the presence of crops, and should not react chemically with the aqueous concentrates or other composition ingredients.
- Such mixtures can be designed for application directly to weeds or their locus or can be concentrates or formulations that are normally diluted with additional carriers and adjuvants before application.
- the surface-active agents can be anionic, cationic or nonionic in character and can be employed as emulsifying agents, wetting agents, suspending agents, or for other purposes.
- Typical surface-active agents include salts of alkyl sulfates, such as diethanolammonium lauryl sulfate; alkylarylsulfonate salts, such as calcium dodecylbenzenesulfonate; alkylphenol-alkylene oxide addition products, such as nonylphenol-Cis ethoxylate; alcohol-alkylene oxide addition products, such as tridecyl alcohol-Ci 6 ethoxylate; soaps, such as sodium stearate; alkylnaphthalenesulfonate salts, such as sodium dibutylnaphthalenesulfonate; dialkyl esters of sulfosuccinate salts, such as sodium di(2-ethylhexyl) sulfosuccinate; sorbitol esters, such as sorbitol oleate; quaternary amines, such as lauryl trimethylammonium chloride; polyethylene glycol esters of fatty
- compositions commonly used in agricultural compositions include compatibilizing agents, antifoam agents, sequestering agents, neutralizing agents and buffers, corrosion inhibitors, dyes, odorants, spreading agents, penetration aids, sticking agents, dispersing agents, thickening agents, freezing point depressants, antimicrobial agents, and the like.
- the compositions may also contain other compatible components, for example, other herbicides, plant growth regulants, fungicides, insecticides, and the like and can be formulated with liquid fertilizers.
- the active ingredient is generally present in a concentration from 5 to 90 weight percent, preferably 20 to 80 weight percent. Such compositions are typically diluted with water before application.
- the diluted compositions usually applied to weeds or the locus of weeds generally contain 0.001 to 2 weight percent active ingredient and preferably contain 0.01 to 1 weight percent.
- the present aqueous concentrates, after dilution in water, can be applied to weeds or their locus by the use of conventional ground or aerial sprayers, by addition to irrigation water and by other conventional means known to those skilled in the art.
- Example 1 is presented to illustrate the various aspects of this invention and should not be construed as limitations to the claims.
- Example 1
- aqueous concentrates The herbicidal auxinic carboxylic acid and choline hydroxide (46 wt% in water) are combined in equimolar amounts in water at room temperature and mixed until a solution is formed to give an aqueous concentrate of the choline salt of the herbicidal auxinic carboxylic acid. Additional inert ingredients may be added to the samples as is well known to those skilled in the art.
- Eye irritation testing was done according to guideline testing requirements specified in: (1) OECD Guideline for the Testing of Chemicals, Procedure 405 (2002), (2) U.S. EPA Health Effects Test Guidelines, OPPTS 870.2400 (1998), (3) JMAFF 12 -Nouan-1847 (2000) and (4) Official Journal of the European Communities, Methods for the Determination of Toxicity, Part B.5 (Eye Irritation), Directive 2004/73/ED, 29 April 2004.
- Test material formulations were administered to New Zealand albino rabbit (3 animals per formulation) to determine the potential to produce eye irritation. The material was applied in a single dose to the conjuctival sac of one eye of each animal. The other eye remained untreated and served as a control. Irritation of the cornea, iris and conjunctivae were evaluated 21 days after application of the test material. Maximum irritation scores to be obtained are 4 for corneal opacity, 2 for ulceris and 10 for conjunctivitis (these values do not take into account the area of cornea evaluated or additional factors used in the calculations). The results are reported as irritation present in the cornea, iris and conjunctivae in the most sensitive animal 21 days after application.
- 2,4-D choline (sample 1 and 2) and 2,4-D choline mixed with glyphosate DMA (sample 8) had the least amount of irritation present 21 days after application compared to the other 2,4-D amine formulations.
- 2,4-D choline mixed with glyphosate DMA (sample 8) had no irritation present after 21 days, and 2,4-D choline alone had no or minimal conjunctivitis after 21 days (score of 1).
- the other 2,4-D amine formulations had corneal opacity ranging from 1-4, ulceris ranging from 0-2 and conjunctivitis ranging from 1-6 after 21 days.
- a triclopyr choline salt was prepared by reacting triclopyr acid with choline hydroxide in equimolar amounts in water at room temperature. Additional inert ingredients were added to prepare a concentrate containing 360 g/1 triclopyr acid equivalent in the form of the choline salt (Sample 10). The composition and amount of the inert ingredients in the Sample 10 formulation were identical to the composition and amount of the inert ingredients in the commercial Garlon ® 3 A Herbicide containing 360 g/1 triclopyr acid equivalent in the form of the triethyl ammonium salt (Sample 11).
- Example 5 A triclopyr choline salt solution prepared by reacting 98.7 g triclopyr acid technical
- Sample 1 (456 gae/1 2,4-D choline salt) was compared to the cold temperature stability of Sample 3 (456 gae/1 2,4-D DMA salt). Whereas Sample 3 was solid at a temperature of -10°C, Sample 1 remained a homogeneous, clear liquid at temperatures as low as -20°C, indicating greatly improved solubility at low temperatures.
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- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
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- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
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Priority Applications (17)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA2795364A CA2795364C (en) | 2010-04-20 | 2011-04-19 | Aqueous herbicidal concentrates of auxinic carboxylic acids with reduced eye irritancy |
RU2012149119/13A RU2560601C2 (en) | 2010-04-20 | 2011-04-19 | Aqueous herbicidal concentrates of auxinic carboxylic acids with reduced eye irritancy |
EP11717419.3A EP2560494B1 (en) | 2010-04-20 | 2011-04-19 | Aqueous herbicidal concentrates of auxinic carboxylic acids with reduced eye irritancy |
CN201180030424.7A CN102946736B (en) | 2010-04-20 | 2011-04-19 | The aqueous herbicidal thing of the auximone carboxylic acid of Eye irritation with reduction |
ES11717419.3T ES2604106T3 (en) | 2010-04-20 | 2011-04-19 | Aqueous herbicidal concentrates of auxinic carboxylic acids with reduced ocular irritant capacity |
LTEP11717419.3T LT2560494T (en) | 2010-04-20 | 2011-04-19 | Aqueous herbicidal concentrates of auxinic carboxylic acids with reduced eye irritancy |
AU2011242995A AU2011242995B2 (en) | 2010-04-20 | 2011-04-19 | Aqueous herbicidal concentrates of auxinic carboxylic acids with reduced eye irritancy |
DK11717419.3T DK2560494T3 (en) | 2010-04-20 | 2011-04-19 | AEROUS HERBICIDE CONCENTRATES OF AUXINIC CARBOXYLIC ACIDS WITH REDUCED EYE IRRITATION |
UAA201213178A UA107379C2 (en) | 2010-04-20 | 2011-04-19 | Aqueous herbicidal concentrates of auxinic carboxylic acids with reduced eye irritancy |
RS20160962A RS55476B1 (en) | 2010-04-20 | 2011-04-19 | Aqueous herbicidal concentrates of auxinic carboxylic acids with reduced eye irritancy |
BR112012026942A BR112012026942B8 (en) | 2010-04-20 | 2011-04-19 | METHOD FOR PREPARING AQUEOUS HERBICIDES CONCENTRATES COMPRISING CHOLINE AND/OR N,N,N-TRIMETHYLETHANOLAMONIUM |
NZ602705A NZ602705A (en) | 2010-04-20 | 2011-04-19 | Aqueous herbicidal concentrates of auxinic carboxylic acids with reduced eye irritancy |
JP2013506217A JP5923083B2 (en) | 2010-04-20 | 2011-04-19 | Aqueous herbicide concentrates of auxinic carboxylic acids with reduced eye irritation |
MX2012012217A MX342936B (en) | 2010-04-20 | 2011-04-19 | Aqueous herbicidal concentrates of auxinic carboxylic acids with reduced eye irritancy. |
IL222492A IL222492A (en) | 2010-04-20 | 2012-10-16 | Aqueous herbicidal concentrates of auxinic carboxylic acids with reduced eye irritancy |
IL240123A IL240123B (en) | 2010-04-20 | 2015-07-23 | Aqueous herbicidal concentrates of auxinic carboxylic acids with reduced eye irritancy |
IL255957A IL255957A (en) | 2010-04-20 | 2017-11-28 | Aqueous herbicidal concentrates of auxinic carboxylic acids with reduced eye irritancy |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US32593910P | 2010-04-20 | 2010-04-20 | |
US61/325,939 | 2010-04-20 |
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WO2011133482A1 true WO2011133482A1 (en) | 2011-10-27 |
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PCT/US2011/032940 WO2011133482A1 (en) | 2010-04-20 | 2011-04-19 | Aqueous herbicidal concentrates of auxinic carboxylic acids with reduced eye irritancy |
Country Status (22)
Country | Link |
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US (1) | US8563473B2 (en) |
EP (2) | EP2560494B1 (en) |
JP (3) | JP5923083B2 (en) |
CN (2) | CN105123692A (en) |
AR (1) | AR083144A1 (en) |
AU (3) | AU2011242995B2 (en) |
BR (1) | BR112012026942B8 (en) |
CA (1) | CA2795364C (en) |
CO (1) | CO6630102A2 (en) |
DK (1) | DK2560494T3 (en) |
ES (1) | ES2604106T3 (en) |
HU (1) | HUE031260T2 (en) |
IL (3) | IL222492A (en) |
LT (1) | LT2560494T (en) |
MX (1) | MX342936B (en) |
NZ (1) | NZ602705A (en) |
PL (1) | PL2560494T3 (en) |
PT (1) | PT2560494T (en) |
RS (1) | RS55476B1 (en) |
RU (1) | RU2560601C2 (en) |
UA (1) | UA107379C2 (en) |
WO (1) | WO2011133482A1 (en) |
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CN102835395A (en) * | 2012-09-28 | 2012-12-26 | 山东潍坊润丰化工有限公司 | Preparation method of MCPA (2-methyl-4-chloro-phenoxyacetic acid) choline water aqua and raw drug |
US9629364B2 (en) | 2012-12-14 | 2017-04-25 | Dow Agrosciences Llc | Synergistic weed control from applications of aminopyralid and clopyralid |
EP3079469A4 (en) * | 2013-12-10 | 2017-06-14 | Dow AgroSciences LLC | Synergistic herbicidal weed control and improved crop tolerance from combinations of 2,4-d-choline and glufosinate in 2,4-d- and glufosinate-tolerant soybeans, corn, cotton |
WO2018060321A1 (en) * | 2016-09-28 | 2018-04-05 | Eucaryo Beheer B.V. | Composition comprising a bioactive molecule |
EP3331360A4 (en) * | 2015-08-07 | 2019-01-09 | Rhodia Operations | Choline salt and ammonium-free adjuvants for water conditioning and agricultural formulations |
US10412964B2 (en) | 2012-12-14 | 2019-09-17 | Dow Agrosciences Llc | Synergistic weed control from applications of aminopyralid and clopyralid |
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WO2011133482A1 (en) * | 2010-04-20 | 2011-10-27 | Dow Agrosciences Llc | Aqueous herbicidal concentrates of auxinic carboxylic acids with reduced eye irritancy |
NZ700218A (en) * | 2012-03-23 | 2016-05-27 | Dow Agrosciences Llc | Aqueous herbicide concentrates containing fatty acid alkyl esters, fatty acid amides, or triglyceride fatty acid esters and methods of use |
CN104768380A (en) * | 2012-09-13 | 2015-07-08 | 美国陶氏益农公司 | Herbicidal compositions comprising aminopyralid and triclopyr |
CN102845423A (en) * | 2012-09-28 | 2013-01-02 | 山东潍坊润丰化工有限公司 | Method for preparing dicamba cholinergic agent and dicamba cholinergic active compound |
CN102835398A (en) * | 2012-09-28 | 2012-12-26 | 山东潍坊润丰化工有限公司 | Method for preparing clopyralid choline aqueous solution and active compound |
CN102845429B (en) * | 2012-09-28 | 2014-08-13 | 山东潍坊润丰化工股份有限公司 | Preparation method of picloram choline water aqua and picloram choline original drug |
CN103086896A (en) * | 2013-01-25 | 2013-05-08 | 山东潍坊润丰化工有限公司 | Method for preparing 2, 4-D choline |
PL3054774T3 (en) * | 2013-10-11 | 2021-08-02 | Dow Agrosciences Llc | Aqueous herbicidal concentrates |
BR102014027711A2 (en) | 2013-11-08 | 2015-09-15 | Dow Agrosciences Llc | pesticide emulsion concentrates containing natural oils or petroleum derivatives and methods of use |
CN103755629B (en) * | 2014-02-10 | 2016-03-30 | 济南科赛基农化工有限公司 | A kind of method and application preparing fluroxypyr salt |
CN103947672A (en) * | 2014-05-13 | 2014-07-30 | 山东潍坊润丰化工股份有限公司 | Water soluble granules of 2, 4-D choline and glyphosate dimethylamine salt and preparation method thereof |
UY37021A (en) * | 2015-12-14 | 2017-07-31 | Dow Agrosciences Llc | COMPOSITIONS AND METHODS RELATED TO HERBICIDE CARBOXYLIC ACIDS SEMISALS |
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CN110740643A (en) * | 2017-06-13 | 2020-01-31 | 孟山都技术公司 | Auxin herbicide mixtures |
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US20220079152A1 (en) * | 2019-01-18 | 2022-03-17 | Sbm Développement Sas | Synergistic herbicidal mixtures and compositions comprising triclopyr and phosphate ester adjuvants |
CA3150582A1 (en) | 2019-08-13 | 2021-02-18 | Bayer Aktiengesellschaft | Benazolin-choline and its use in the agrochemical field |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2018776A (en) * | 1978-04-15 | 1979-10-24 | Meiji Seika Kaisha | Herbicidal compounds preparation thereof and herbicides containing the same |
US5118444A (en) * | 1991-04-10 | 1992-06-02 | Witco Corporation | Aqueous agricultural compositions exhibiting reduced irritation and corrosion |
WO2008106107A1 (en) | 2007-02-26 | 2008-09-04 | Dow Agrosciences Llc | Compounds derived from herbicidal carboxylic acids and tetraalkylammonium or (arylalkyl) trialkylammonium hydroxides |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS51106728A (en) * | 1975-03-12 | 1976-09-21 | Mitsubishi Gas Chemical Co | JOSOZAI |
ZA200600081B (en) * | 2003-08-04 | 2007-03-28 | Dow Agrosciences Llc | High-strength, low viscosity herbicidal formulations of glyphosate |
BR122016000119B8 (en) * | 2007-06-29 | 2022-06-28 | Dow Agrosciences Llc | HERBICIDAL MIXTURE COMPRISING POTASSIUM DICHLORPROPE SALT AND ISOPROPYLAMINE GLYPHOSATE SALT, HERBICIDAL COMPOSITION, AND METHOD FOR CONTROL OF UNDESIRABLE VEGETATION |
WO2011133482A1 (en) * | 2010-04-20 | 2011-10-27 | Dow Agrosciences Llc | Aqueous herbicidal concentrates of auxinic carboxylic acids with reduced eye irritancy |
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2011
- 2011-04-19 WO PCT/US2011/032940 patent/WO2011133482A1/en active Application Filing
- 2011-04-19 JP JP2013506217A patent/JP5923083B2/en active Active
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- 2011-04-19 CN CN201510452364.8A patent/CN105123692A/en active Pending
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- 2011-04-19 LT LTEP11717419.3T patent/LT2560494T/en unknown
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- 2011-04-19 EP EP16168097.0A patent/EP3066926A3/en not_active Withdrawn
- 2011-04-19 UA UAA201213178A patent/UA107379C2/en unknown
- 2011-04-19 BR BR112012026942A patent/BR112012026942B8/en active IP Right Grant
- 2011-04-19 MX MX2012012217A patent/MX342936B/en active IP Right Grant
- 2011-04-19 CN CN201180030424.7A patent/CN102946736B/en active Active
- 2011-04-20 AR ARP110101389A patent/AR083144A1/en not_active Application Discontinuation
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2012
- 2012-10-08 CO CO12176892A patent/CO6630102A2/en active IP Right Grant
- 2012-10-16 IL IL222492A patent/IL222492A/en active IP Right Grant
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2015
- 2015-02-17 AU AU2015200797A patent/AU2015200797B2/en active Active
- 2015-07-23 IL IL240123A patent/IL240123B/en active IP Right Grant
- 2015-12-22 JP JP2015249355A patent/JP6368701B2/en active Active
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2017
- 2017-03-07 AU AU2017201552A patent/AU2017201552A1/en not_active Abandoned
- 2017-04-11 JP JP2017077984A patent/JP2017160218A/en not_active Withdrawn
- 2017-11-28 IL IL255957A patent/IL255957A/en unknown
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2018776A (en) * | 1978-04-15 | 1979-10-24 | Meiji Seika Kaisha | Herbicidal compounds preparation thereof and herbicides containing the same |
US5118444A (en) * | 1991-04-10 | 1992-06-02 | Witco Corporation | Aqueous agricultural compositions exhibiting reduced irritation and corrosion |
WO2008106107A1 (en) | 2007-02-26 | 2008-09-04 | Dow Agrosciences Llc | Compounds derived from herbicidal carboxylic acids and tetraalkylammonium or (arylalkyl) trialkylammonium hydroxides |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102835395A (en) * | 2012-09-28 | 2012-12-26 | 山东潍坊润丰化工有限公司 | Preparation method of MCPA (2-methyl-4-chloro-phenoxyacetic acid) choline water aqua and raw drug |
US9629364B2 (en) | 2012-12-14 | 2017-04-25 | Dow Agrosciences Llc | Synergistic weed control from applications of aminopyralid and clopyralid |
US10412964B2 (en) | 2012-12-14 | 2019-09-17 | Dow Agrosciences Llc | Synergistic weed control from applications of aminopyralid and clopyralid |
US12022831B2 (en) | 2012-12-14 | 2024-07-02 | Corteva Agriscience Llc | Synergistic weed control from applications of aminopyralid and clopyralid |
EP3079469A4 (en) * | 2013-12-10 | 2017-06-14 | Dow AgroSciences LLC | Synergistic herbicidal weed control and improved crop tolerance from combinations of 2,4-d-choline and glufosinate in 2,4-d- and glufosinate-tolerant soybeans, corn, cotton |
EP3079470A4 (en) * | 2013-12-10 | 2017-06-21 | Dow AgroSciences LLC | Synergistic herbicidal weed control from combinations of 2,4-d-choline and glufosinate |
EP3331360A4 (en) * | 2015-08-07 | 2019-01-09 | Rhodia Operations | Choline salt and ammonium-free adjuvants for water conditioning and agricultural formulations |
AU2021201043B2 (en) * | 2015-08-07 | 2022-06-16 | Specialty Operations France | Choline salt and ammonium-free adjuvants for water conditioning and agricultural formulations |
WO2018060321A1 (en) * | 2016-09-28 | 2018-04-05 | Eucaryo Beheer B.V. | Composition comprising a bioactive molecule |
US11839217B2 (en) | 2016-09-28 | 2023-12-12 | Eucaryo Beheer B.V. | Composition comprising a bioactive molecule |
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