CA2396051A1 - Aqueous, herbicidal means - Google Patents
Aqueous, herbicidal means Download PDFInfo
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- CA2396051A1 CA2396051A1 CA002396051A CA2396051A CA2396051A1 CA 2396051 A1 CA2396051 A1 CA 2396051A1 CA 002396051 A CA002396051 A CA 002396051A CA 2396051 A CA2396051 A CA 2396051A CA 2396051 A1 CA2396051 A1 CA 2396051A1
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- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/34—Nitriles
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- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
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- Engineering & Computer Science (AREA)
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- General Health & Medical Sciences (AREA)
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Abstract
The invention relates to an aqueous means containing bromoxynil or the derivatives thereof. The invention also relates to compounds of the general formula (I): RO-(C2H4O)n(C3H6O)m-R', wherein RO stands for an alcohol radical selected from the group of the branched or linear, saturated or unsaturated, monovalent alcohols having 1 to 6 C atoms or of the polyols having 2 to 12 C
atoms and 2 to 6 hydroxyl groups and R' stands for hydrogen and/or an ester group -CO-R'', wherein R'' means a branched or linear, saturated or unsaturated alkyl radical having 5 to 29 C atoms, n is a number between 1 and 50 and m is zero or a number between 1 and 10. An increased amount of the active agent penetrates the plant.
atoms and 2 to 6 hydroxyl groups and R' stands for hydrogen and/or an ester group -CO-R'', wherein R'' means a branched or linear, saturated or unsaturated alkyl radical having 5 to 29 C atoms, n is a number between 1 and 50 and m is zero or a number between 1 and 10. An increased amount of the active agent penetrates the plant.
Description
Aqueous, Herbicidal Means This invention relates to water-based herbicidal preparations containing at least one agrochemical agent from the group consisting of bromoxynil and its derivatives and certain alkoxylated fatty acid esters, to the use of such fatty acid esters for increasing the penetration of bromoxynil and its derivatives into plant leaves and to a process for controlling unwanted plant growth.
It is known that weeds can be controlled with a variety of herbicides which often have little or no solubility in water. One important representative is bromoxynil (3,5-dibromo-4-hydroxybenzonitrile) and its derivatives. Where herbicidal agents such as these are applied, penetration into the plant is minimal on account of their poor solubility in water, resulting in an inadequate herbicidal effect. Accordingly, agrochemical agents of the type in question are formulated as aqueous dispersions or emulsions so that they can be applied without difficulty, for example by spraying onto the plants, the emulsifier also acting as a wetting agent to improve uptake of the agent into the plant. The greater the penetration of the herbicide, the more effectively and efficiently it can be used. Accordingly, there is a general need for formulations which provide for substantially complete penetration of the herbicidal agent into the plant.
DE-OS 29 24 403, for example, describes water-based preparations containing bromoxynil salts and - as formulation aids - alkali metal salts of alkyl p olyglycol a ther p hosphate p artial esters. E P 0 485 207 describes aqueous emulsions containing bromoxynil octanoate and heptanoate and, as emulsifiers, polyalkylene oxide-modified silanes or ethoxylated tall oil amides.
It has surprisingly been found that water-based preparations containing bromoxynil or derivatives thereof and, as emulsifiers, certain alkoxylated alcohols provide for very high penetration of the herbicide into the plant.
Accordingly, the present invention relates to water-based preparations containing bromoxynil or derivatives thereof and one or more compounds corresponding to general formula (I):
RO-(C2H40)n(C3H60)m-R' (.l ) in which RO is an alcohol selected from the group of branched or linear, saturated or unsaturated monohydric alcohols containing 1 to 6 carbon atoms or polyols containing 2 to 12 carbon atoms and 2 to 6 hydroxyl groups and R' is hydrogen andlor a group -CO-R", where R" is a branched or linear, saturated or unsaturated alkyl g roup c ontaining 5 t o 2 9 c arbon atoms, n is a number of 1 to 50 and m is 0 or a number of 1 to 10.
The preparations according to the invention contain bromoxynil andlor derivatives thereof, preferably bromoxynil alkyl esters or sodium andlor p otassium s alts of bromoxynil o r s ulfates a nd c arbonates t hereof.
Preparations containing bromoxynil octanoate or heptanoate are particularly preferred.
The alkoxylated compounds corresponding to formula (I) are known substances which are described, for example, in US 2,678,935, US
It is known that weeds can be controlled with a variety of herbicides which often have little or no solubility in water. One important representative is bromoxynil (3,5-dibromo-4-hydroxybenzonitrile) and its derivatives. Where herbicidal agents such as these are applied, penetration into the plant is minimal on account of their poor solubility in water, resulting in an inadequate herbicidal effect. Accordingly, agrochemical agents of the type in question are formulated as aqueous dispersions or emulsions so that they can be applied without difficulty, for example by spraying onto the plants, the emulsifier also acting as a wetting agent to improve uptake of the agent into the plant. The greater the penetration of the herbicide, the more effectively and efficiently it can be used. Accordingly, there is a general need for formulations which provide for substantially complete penetration of the herbicidal agent into the plant.
DE-OS 29 24 403, for example, describes water-based preparations containing bromoxynil salts and - as formulation aids - alkali metal salts of alkyl p olyglycol a ther p hosphate p artial esters. E P 0 485 207 describes aqueous emulsions containing bromoxynil octanoate and heptanoate and, as emulsifiers, polyalkylene oxide-modified silanes or ethoxylated tall oil amides.
It has surprisingly been found that water-based preparations containing bromoxynil or derivatives thereof and, as emulsifiers, certain alkoxylated alcohols provide for very high penetration of the herbicide into the plant.
Accordingly, the present invention relates to water-based preparations containing bromoxynil or derivatives thereof and one or more compounds corresponding to general formula (I):
RO-(C2H40)n(C3H60)m-R' (.l ) in which RO is an alcohol selected from the group of branched or linear, saturated or unsaturated monohydric alcohols containing 1 to 6 carbon atoms or polyols containing 2 to 12 carbon atoms and 2 to 6 hydroxyl groups and R' is hydrogen andlor a group -CO-R", where R" is a branched or linear, saturated or unsaturated alkyl g roup c ontaining 5 t o 2 9 c arbon atoms, n is a number of 1 to 50 and m is 0 or a number of 1 to 10.
The preparations according to the invention contain bromoxynil andlor derivatives thereof, preferably bromoxynil alkyl esters or sodium andlor p otassium s alts of bromoxynil o r s ulfates a nd c arbonates t hereof.
Preparations containing bromoxynil octanoate or heptanoate are particularly preferred.
The alkoxylated compounds corresponding to formula (I) are known substances which are described, for example, in US 2,678,935, US
3,539,518, US 4,022,808 or GB 1 ,050,497 of which the disclosures are also part of the present invention.
The compounds corresponding to formula (I) may by prepared by any methods known to the expert, for example by esterification of fatty acids with alkoxylated methanol, as described in US 3,539,518.
Unfortunately, this process has certain disadvantages. It is a two-stage process, the esterification reaction is very time-consuming and the products are colored by the high reaction temperatures. In addition, fatty acid methylester ethoxylates produced by this process have relatively high OH
values after the esterification step which can be problematical for certain applications. Another possibility is the direct reaction of fatty acid esters with alkylene oxides in the presence of transition metal catalysts, as described in US 4,022,808. However, the fatty acid alkyl ester alkoxylates are preferably produced by the heterogeneously catalyzed direct alkoxylation of fatty acid alkyl esters with ethylene oxide and/or propylene oxide on calcined or hydrophobicized hydrotalcites. These synthesis processes are d escribed i n d etail i n W O 90113533 a nd W O 91!15441 of which t he d isclosure i s a Iso part of t he present i nvention. T he p roducts formed are distinguished by a low OH value, the reaction is carried out in a single stage and light-colored products are obtained. The fatty acid alkyl esters used as starting materials may be obtained from natural oils and fats or may be synthetically produced.
The alkoxylated fatty acid esters contain at least 1 mol ethylene oxide groups per mol ester. Compounds of formula (I) containing between 1 and 30 mol ethylene oxide per mol ester are preferred. In addition to the ethylene oxide units, between 1 and 10 propylene oxide groups are also present in the molecule. Other preferred compounds corresponding to formula (I) are those which contain between 1 and 30 mol ethylene oxide per mol ester and 1 to 10 mol propylene oxide groups. For these mixed ethylene oxidelpropylene oxide adducts, it is possible to use both compounds reacted with a mixture of ethylene oxide and propylene oxide and compounds reacted with ethylene oxide and p ropylene oxide in two separate steps. The alkoxides are statistically distributed between the OH
groups present, depending on the production process.
If compounds corresponding to formula (I) containing polyols as the alcohol component RO are used, the quantitative data for the ethylene or propylene oxide units (indices n and m) are always based on the molecule as a whole. However, the exact distribution of the ethylene or propylene oxide units between the various hydroxyl groups of the polyols is known to comply with a distribution dependent on the synthesis process.
The f atty acid esters -CO-R" contain alkyl groups R" with 5 to 29 carbon atoms. Suitable fatty acid components are natural or synthetic fatty acids, more particularly straight-chain, saturated or unsaturated C~3o fatty acids, including technical mixtures thereof obtainable by lipolysis from animal and vegetable fats and oils, for example from coconut oil, palm kernel oil, soybean oil, sunflower oil, rapeseed oil, cottonseed oil, fish oil, bovine tallow and lard; special examples are caprylic, capric, lauric, lauroleic, myristic, m yristoleic, p almitic, p almitoleic, oleic, elaidic, arachic, gadoleic, behenic and erucic acid.
Suitable alcohol components RO are linear or branched, saturated or unsaturated monohydric alcohols containing 1 to 6 carbon atoms, for example methanol, ethanol, n- and i-propanol, n- and i-butanol, pentanol, hexanol, 2-ethylhexanol and cyclohexanol. Suitable C2_6 polyols are, for example, ethylene glycol, 1,2-propylene glycol, 1,2-butylene glycol, glycerol or trimethylol propane and pentaerythritol.
Basically, all the hydroxyl groups of the alcohols are substituted by the alkoxides although not all terminal alkoxide groups are capped by ester groups. Accordingly, if polyols, such as glycerol or ethylene glycol, are used as the alcohol component RO, the preparations may contain compounds corresponding to formula (I) obtained by reaction both of the full esters and of the partial esters with alkoxides. However, preferred compounds of formula (I) are those in which all the hydroxyl groups of the alcohols a re alkoxylated and all terminal alkoxide groups are capped by ester groups with the formula -CO-R". Accordingly, in these preferred compounds, R" in formula (I) stands exclusively for a branched or linear, saturated or unsaturated alkyl group containing 5 to 29 carbon atoms.
In addition, alkoxylated fatty acid esters corresponding to formula (I) of which the fatty acid component is selected from linear, unbranched C~~a fatty acids and of which the alcohol component is methanol, the esters (I) preferably containing between 1 and 3 mol propylene oxide and between 1 and 6 mol ethylene oxide per mol ester, are preferably used in the preparations according to the invention. Compounds such as these can be obtained, for example, by the above-described reactions of palmitic, 5 stearic, oleic, linoleic or linolenic acid, lauric acid and myristic acid or esters thereof with alkoxides.
Also suitable are alkoxylated compounds where the alcohol component is glycerol and the fatty acid component is selected from saturated or unsaturated, branched or unbranched fatty acids containing 18 to 22 carbon atoms and the esters contain between 1 and 3 mol ethylene oxide per mol ester. Compounds of formula (I) in which n is 5, 10 or 30 and m is 0 are particularly preferred. Compounds such as these can be obtained, for example, by reacting glycerol esters of natural fatty acids, such as, for example, palm oil, rapeseed oil, soybean oil or preferably castor oil, with ethylene oxide.
The compounds of formula (I) present in the preparations according to the invention are nonionic compounds which may also be characterized by their HLB value (hydrophilicllipophilic balance according to Griffin's definition; see Rompp, Lexikon Chemie, 10th Edition 1997, page 1764).
Preferred preparations contain compounds of formula (I) with HLB values of 4 to 10 and preferably 5 to 9.
The preparations contain at least bromoxynil or derivatives thereof as herbicides although mixtures with various other herbicides may also be used. The preparations according to the invention may contain the herbicide in enriched form, in which case they are formulated as concentrates containing more than 50% by weight to at most 90% by weight of herbicidal agent. However, they may also be present i n d flute form. Preferred preparations contain between 0.01 and 5% by weight of bromoxynil or derivatives thereof, based on the weight of the preparation.
If the preparations contain other agrochemical agents, they are present in quantities of 0.01 to 10% by weight. The percentage water content of the preparations according to the invention is preferably between 10 and 99.9% by weight. The quantity ratio between the compounds of formula (I) and the herbicidal agents is preferably between 1:1 and 1:100. Particularly preferred preparations are those in which the ratio by weight between the compounds of formula ( I) a nd t he herbicidal a gents is in the range f rom 1:10 to 1:80 and more particularly in the range from 1:2 to 1:5.
Besides bromoxynil and its derivatives and the compounds of formula ( I), t he water-based p reparations a ccording to t he i nvention may contain other typical ingredients and additives. These include solvents, such as ethylene or propylene glycols and C~_6 alcohols, solid carriers, such a s I ignin, I ignin d erivatives o r c lays a nd o they k nown a mulsifiers or dispersants. However, preparations containing only emulsifiers corresponding to formula (I) and no other emulsifiers or dispersants are particularly preferred. Most particularly preferred preparations are those which are free from colloids, such as titanium dioxide, andlor free from solvents, more particularly mineral-oil-based solvents.
The preparations a ccording to the invention are stable in storage, even at temperatures above 30°C, and can be produced without intensive shearing, for example by manual stirring. The preparations according to the invention are formed without intensive shearing, for example by simple manual stirring. To this end, the compounds of formula (I) may be initially introduced into a mixing vessel, for example in liquid form. The herbicidal agent is then added and the resulting mixture is dispersed in water. If compounds of formula (I) with melting points above room temperature are used, they may be used in molten form. However, compounds corresponding to formula (I) with a melting point below 25°C are preferably used. Alternatively, a mixture of the agrochemical agent in water may also be prepared in a first step and the mixture thus prepared may be subsequently emulsified or dispersed by addition of compounds corresponding to formula (I).
The present invention also relates to a process for controlling unwanted plants in which a water-based bromoxynil-containing preparation as described in the foregoing is applied to the leaves of the plants by any method known to the expert in such quantities that the plants die off.
The present invention also relates to the use of compounds corresponding to formula (I) for increasing the penetration of bromoxynil or its derivatives into plant leaves.
Examples Six aqueous bromoxynil Na salt emulsions were prepared. They were either free from emulsifiers or contained known emulsifiers and were compared with a preparation according to the invention containing as additive a compound corresponding to formula (I) in which RO = glycerol, R' = COR" with R" = C~s_~8, m = 0, n = 30.
The emulsifiers were present in quantities of 0.5% by weight, based on the preparation as a whole. The concentration of the sodium salt of the bromoxynil was 4.1 mM. Quantities of 0.1 p1 of the water-based preparations were applied to the first leaves of deadly nightshade.
Penetration into the leaves was measured after 24 hours. The results are set out in Table 2.
Table 1:
Test Emulsifier (1 ) -(2) C$_~o Alkyl (oligo)glucoside (3) C6_~o Fatty acid methyl ester + 3 EO
(4) C6_~o Fatty acid methyl ester + 6 EO
(5) Nonylphenol + 10 EO
(6) Triglyceride according to the invention Table 2:
Test Penetration after 24 h in (1 ) 0 (2) 2 (3) 22 (4) 56 (5) 42 (6) 82 The results show the increase in the penetration of bromoxynil achieved by adding the preparations according to the invention.
The compounds corresponding to formula (I) may by prepared by any methods known to the expert, for example by esterification of fatty acids with alkoxylated methanol, as described in US 3,539,518.
Unfortunately, this process has certain disadvantages. It is a two-stage process, the esterification reaction is very time-consuming and the products are colored by the high reaction temperatures. In addition, fatty acid methylester ethoxylates produced by this process have relatively high OH
values after the esterification step which can be problematical for certain applications. Another possibility is the direct reaction of fatty acid esters with alkylene oxides in the presence of transition metal catalysts, as described in US 4,022,808. However, the fatty acid alkyl ester alkoxylates are preferably produced by the heterogeneously catalyzed direct alkoxylation of fatty acid alkyl esters with ethylene oxide and/or propylene oxide on calcined or hydrophobicized hydrotalcites. These synthesis processes are d escribed i n d etail i n W O 90113533 a nd W O 91!15441 of which t he d isclosure i s a Iso part of t he present i nvention. T he p roducts formed are distinguished by a low OH value, the reaction is carried out in a single stage and light-colored products are obtained. The fatty acid alkyl esters used as starting materials may be obtained from natural oils and fats or may be synthetically produced.
The alkoxylated fatty acid esters contain at least 1 mol ethylene oxide groups per mol ester. Compounds of formula (I) containing between 1 and 30 mol ethylene oxide per mol ester are preferred. In addition to the ethylene oxide units, between 1 and 10 propylene oxide groups are also present in the molecule. Other preferred compounds corresponding to formula (I) are those which contain between 1 and 30 mol ethylene oxide per mol ester and 1 to 10 mol propylene oxide groups. For these mixed ethylene oxidelpropylene oxide adducts, it is possible to use both compounds reacted with a mixture of ethylene oxide and propylene oxide and compounds reacted with ethylene oxide and p ropylene oxide in two separate steps. The alkoxides are statistically distributed between the OH
groups present, depending on the production process.
If compounds corresponding to formula (I) containing polyols as the alcohol component RO are used, the quantitative data for the ethylene or propylene oxide units (indices n and m) are always based on the molecule as a whole. However, the exact distribution of the ethylene or propylene oxide units between the various hydroxyl groups of the polyols is known to comply with a distribution dependent on the synthesis process.
The f atty acid esters -CO-R" contain alkyl groups R" with 5 to 29 carbon atoms. Suitable fatty acid components are natural or synthetic fatty acids, more particularly straight-chain, saturated or unsaturated C~3o fatty acids, including technical mixtures thereof obtainable by lipolysis from animal and vegetable fats and oils, for example from coconut oil, palm kernel oil, soybean oil, sunflower oil, rapeseed oil, cottonseed oil, fish oil, bovine tallow and lard; special examples are caprylic, capric, lauric, lauroleic, myristic, m yristoleic, p almitic, p almitoleic, oleic, elaidic, arachic, gadoleic, behenic and erucic acid.
Suitable alcohol components RO are linear or branched, saturated or unsaturated monohydric alcohols containing 1 to 6 carbon atoms, for example methanol, ethanol, n- and i-propanol, n- and i-butanol, pentanol, hexanol, 2-ethylhexanol and cyclohexanol. Suitable C2_6 polyols are, for example, ethylene glycol, 1,2-propylene glycol, 1,2-butylene glycol, glycerol or trimethylol propane and pentaerythritol.
Basically, all the hydroxyl groups of the alcohols are substituted by the alkoxides although not all terminal alkoxide groups are capped by ester groups. Accordingly, if polyols, such as glycerol or ethylene glycol, are used as the alcohol component RO, the preparations may contain compounds corresponding to formula (I) obtained by reaction both of the full esters and of the partial esters with alkoxides. However, preferred compounds of formula (I) are those in which all the hydroxyl groups of the alcohols a re alkoxylated and all terminal alkoxide groups are capped by ester groups with the formula -CO-R". Accordingly, in these preferred compounds, R" in formula (I) stands exclusively for a branched or linear, saturated or unsaturated alkyl group containing 5 to 29 carbon atoms.
In addition, alkoxylated fatty acid esters corresponding to formula (I) of which the fatty acid component is selected from linear, unbranched C~~a fatty acids and of which the alcohol component is methanol, the esters (I) preferably containing between 1 and 3 mol propylene oxide and between 1 and 6 mol ethylene oxide per mol ester, are preferably used in the preparations according to the invention. Compounds such as these can be obtained, for example, by the above-described reactions of palmitic, 5 stearic, oleic, linoleic or linolenic acid, lauric acid and myristic acid or esters thereof with alkoxides.
Also suitable are alkoxylated compounds where the alcohol component is glycerol and the fatty acid component is selected from saturated or unsaturated, branched or unbranched fatty acids containing 18 to 22 carbon atoms and the esters contain between 1 and 3 mol ethylene oxide per mol ester. Compounds of formula (I) in which n is 5, 10 or 30 and m is 0 are particularly preferred. Compounds such as these can be obtained, for example, by reacting glycerol esters of natural fatty acids, such as, for example, palm oil, rapeseed oil, soybean oil or preferably castor oil, with ethylene oxide.
The compounds of formula (I) present in the preparations according to the invention are nonionic compounds which may also be characterized by their HLB value (hydrophilicllipophilic balance according to Griffin's definition; see Rompp, Lexikon Chemie, 10th Edition 1997, page 1764).
Preferred preparations contain compounds of formula (I) with HLB values of 4 to 10 and preferably 5 to 9.
The preparations contain at least bromoxynil or derivatives thereof as herbicides although mixtures with various other herbicides may also be used. The preparations according to the invention may contain the herbicide in enriched form, in which case they are formulated as concentrates containing more than 50% by weight to at most 90% by weight of herbicidal agent. However, they may also be present i n d flute form. Preferred preparations contain between 0.01 and 5% by weight of bromoxynil or derivatives thereof, based on the weight of the preparation.
If the preparations contain other agrochemical agents, they are present in quantities of 0.01 to 10% by weight. The percentage water content of the preparations according to the invention is preferably between 10 and 99.9% by weight. The quantity ratio between the compounds of formula (I) and the herbicidal agents is preferably between 1:1 and 1:100. Particularly preferred preparations are those in which the ratio by weight between the compounds of formula ( I) a nd t he herbicidal a gents is in the range f rom 1:10 to 1:80 and more particularly in the range from 1:2 to 1:5.
Besides bromoxynil and its derivatives and the compounds of formula ( I), t he water-based p reparations a ccording to t he i nvention may contain other typical ingredients and additives. These include solvents, such as ethylene or propylene glycols and C~_6 alcohols, solid carriers, such a s I ignin, I ignin d erivatives o r c lays a nd o they k nown a mulsifiers or dispersants. However, preparations containing only emulsifiers corresponding to formula (I) and no other emulsifiers or dispersants are particularly preferred. Most particularly preferred preparations are those which are free from colloids, such as titanium dioxide, andlor free from solvents, more particularly mineral-oil-based solvents.
The preparations a ccording to the invention are stable in storage, even at temperatures above 30°C, and can be produced without intensive shearing, for example by manual stirring. The preparations according to the invention are formed without intensive shearing, for example by simple manual stirring. To this end, the compounds of formula (I) may be initially introduced into a mixing vessel, for example in liquid form. The herbicidal agent is then added and the resulting mixture is dispersed in water. If compounds of formula (I) with melting points above room temperature are used, they may be used in molten form. However, compounds corresponding to formula (I) with a melting point below 25°C are preferably used. Alternatively, a mixture of the agrochemical agent in water may also be prepared in a first step and the mixture thus prepared may be subsequently emulsified or dispersed by addition of compounds corresponding to formula (I).
The present invention also relates to a process for controlling unwanted plants in which a water-based bromoxynil-containing preparation as described in the foregoing is applied to the leaves of the plants by any method known to the expert in such quantities that the plants die off.
The present invention also relates to the use of compounds corresponding to formula (I) for increasing the penetration of bromoxynil or its derivatives into plant leaves.
Examples Six aqueous bromoxynil Na salt emulsions were prepared. They were either free from emulsifiers or contained known emulsifiers and were compared with a preparation according to the invention containing as additive a compound corresponding to formula (I) in which RO = glycerol, R' = COR" with R" = C~s_~8, m = 0, n = 30.
The emulsifiers were present in quantities of 0.5% by weight, based on the preparation as a whole. The concentration of the sodium salt of the bromoxynil was 4.1 mM. Quantities of 0.1 p1 of the water-based preparations were applied to the first leaves of deadly nightshade.
Penetration into the leaves was measured after 24 hours. The results are set out in Table 2.
Table 1:
Test Emulsifier (1 ) -(2) C$_~o Alkyl (oligo)glucoside (3) C6_~o Fatty acid methyl ester + 3 EO
(4) C6_~o Fatty acid methyl ester + 6 EO
(5) Nonylphenol + 10 EO
(6) Triglyceride according to the invention Table 2:
Test Penetration after 24 h in (1 ) 0 (2) 2 (3) 22 (4) 56 (5) 42 (6) 82 The results show the increase in the penetration of bromoxynil achieved by adding the preparations according to the invention.
Claims (14)
1. A herbicidal preparation containing water and bromoxynil and/or derivatives thereof, characterized in that it also contains at least one or more compounds corresponding to general formula (I):
RO-(C2H4O)n(C3H6O)m-R' (I) in which RO is an alcohol selected from the group of branched or linear, saturated or unsaturated monohydric alcohols containing 1 to 6 carbon atoms or polyols containing 2 to 12 carbon atoms and 2 to 6 hydroxyl groups and R' is hydrogen and/or an ester group -CO-R", where R" is a branched or linear, saturated or unsaturated alkyl group containing 5 to 29 carbon atoms, n is a number of 1 to 50 and m is 0 or a number of 1 to 10.
RO-(C2H4O)n(C3H6O)m-R' (I) in which RO is an alcohol selected from the group of branched or linear, saturated or unsaturated monohydric alcohols containing 1 to 6 carbon atoms or polyols containing 2 to 12 carbon atoms and 2 to 6 hydroxyl groups and R' is hydrogen and/or an ester group -CO-R", where R" is a branched or linear, saturated or unsaturated alkyl group containing 5 to 29 carbon atoms, n is a number of 1 to 50 and m is 0 or a number of 1 to 10.
2. A preparation as claimed in claim 1, characterized in that, in the compounds of formula (I), R" stands exclusively for a branched or linear, saturated or unsaturated alkyl group containing 5 to 29 carbon atoms.
3. A preparation as claimed in claim 1 or 2, characterized in that, in the compounds of formula (I), RO is glycerol and R" is a branched or linear, saturated or unsaturated alkyl group containing 17 to 21 carbon atoms.
4. A preparation as claimed in claims 1 to 3, characterized in that, in the compounds of formula (I), n is a number of 1 to 30 and m is 0 or a number of 1 to 5.
5. A preparation as claimed in any of claims 1 to 4, characterized in that, in the compounds of formula (I), n = 5, 10 or 30 and m is 0.
6. A preparation as claimed in claims 1 to 5, characterized in that, in the compounds of formula (I), -CO-R" is ricinoleic acid and RO is glycerol.
7. A preparation as claimed in claim 1, characterized in that, in the compounds of formula (I), RO is methanol and R" is a branched or linear, saturated or unsaturated alkyl group containing 5 to 17 carbon atoms.
8. A preparation as claimed in any of claims 1 to 7, characterized in that the compounds of formula (I) have an HLB value of 4 to 10.
9. A preparation as claimed in any of claims 1 to 8, characterized in that it contains between 0.01 and 5% by weight of bromoxynil or a derivative thereof.
10. A preparation as claimed in any of claims 1 to 9, characterized in that it contains a bromoxynil alkyl ester, preferably bromoxynil octanoate or heptanoate.
11. A preparation as claimed in any of claims 1 to 10, characterized in that it contains sodium and/or potassium salts of bromoxynil.
12. A preparation as claimed in any of claims 1 to 11, characterized in that it is free from colloidal material.
13. A process for controlling unwanted plants, characterized in that the water-based preparation claimed in claim 1 is applied to the leaves of the unwanted plant in such quantities that the plant dies off.
14. The use of compounds corresponding to formula (I) for increasing the penetration of bromoxynil or derivatives thereof into plant leaves.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10000320.6 | 2000-01-07 | ||
| DE2000100320 DE10000320A1 (en) | 2000-01-07 | 2000-01-07 | Aqueous herbicidal agent |
| PCT/EP2000/013266 WO2001050861A1 (en) | 2000-01-07 | 2000-12-23 | Aqueous, herbicidal means |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2396051A1 true CA2396051A1 (en) | 2001-07-19 |
Family
ID=7626857
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002396051A Abandoned CA2396051A1 (en) | 2000-01-07 | 2000-12-23 | Aqueous, herbicidal means |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP1246531A1 (en) |
| AU (1) | AU3164301A (en) |
| BR (1) | BR0016923A (en) |
| CA (1) | CA2396051A1 (en) |
| DE (1) | DE10000320A1 (en) |
| WO (1) | WO2001050861A1 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20080172937A1 (en) * | 2007-01-24 | 2008-07-24 | Charles Francis Palmer | Method for improving the water transport characteristics of hydrophobic surfaces |
| US8658130B2 (en) | 2009-02-13 | 2014-02-25 | Cognis Ip Management Gmbh | Agricultural compositions |
| US9107403B2 (en) | 2008-12-23 | 2015-08-18 | Cognis Ip Management Gmbh | Agrochemical auxiliary compositions |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10063960A1 (en) | 2000-12-20 | 2002-06-27 | Aventis Cropscience Gmbh | Herbicidal agents |
| EP2266394A1 (en) | 2009-06-17 | 2010-12-29 | Cognis IP Management GmbH | Non-aqueous agricultural compositions |
| EP2329715B1 (en) | 2009-12-01 | 2013-02-20 | Cognis IP Management GmbH | Biocide compositions comprising branched alkyl polyglycosides |
| EP2384624B1 (en) * | 2010-05-08 | 2015-04-15 | Cognis IP Management GmbH | Biocide compositions comprising alkoxylated oligoglycerol esters |
| HUE056399T2 (en) * | 2012-01-23 | 2022-02-28 | Syngenta Participations Ag | Adjuvant compositions |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2591069B1 (en) * | 1985-12-09 | 1988-03-18 | Produits Ind Cie Fse | HERBICIDE PRODUCTS BASED ON BROMOXYNIL ESTERS AND / OR IXXYNIL |
| GB8612094D0 (en) * | 1986-05-19 | 1986-06-25 | May & Baker Ltd | Compositions of matter |
| DD268147A1 (en) * | 1988-01-13 | 1989-05-24 | Akad Wissenschaften Ddr | HERBICIDAL AGENT |
| DE19908559A1 (en) * | 1999-02-27 | 2000-09-07 | Cognis Deutschland Gmbh | PIT emulsions |
-
2000
- 2000-01-07 DE DE2000100320 patent/DE10000320A1/en not_active Withdrawn
- 2000-12-23 AU AU31643/01A patent/AU3164301A/en not_active Abandoned
- 2000-12-23 EP EP00991267A patent/EP1246531A1/en not_active Withdrawn
- 2000-12-23 WO PCT/EP2000/013266 patent/WO2001050861A1/en not_active Application Discontinuation
- 2000-12-23 BR BR0016923-4A patent/BR0016923A/en not_active Application Discontinuation
- 2000-12-23 CA CA002396051A patent/CA2396051A1/en not_active Abandoned
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20080172937A1 (en) * | 2007-01-24 | 2008-07-24 | Charles Francis Palmer | Method for improving the water transport characteristics of hydrophobic surfaces |
| US9487698B2 (en) * | 2007-01-24 | 2016-11-08 | Ethox Chemicals, Llc | Method for improving the water transport characteristics of hydrophobic surfaces |
| US9107403B2 (en) | 2008-12-23 | 2015-08-18 | Cognis Ip Management Gmbh | Agrochemical auxiliary compositions |
| US8658130B2 (en) | 2009-02-13 | 2014-02-25 | Cognis Ip Management Gmbh | Agricultural compositions |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2001050861A1 (en) | 2001-07-19 |
| AU3164301A (en) | 2001-07-24 |
| BR0016923A (en) | 2002-12-31 |
| EP1246531A1 (en) | 2002-10-09 |
| DE10000320A1 (en) | 2001-07-12 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |