Patent Grant
6992047
(1) Field of the Invention
The present invention relates to methods for the microencapsulation of an agricultural active having a high melting point, and more particularly to methods for the microencapsulation of such material while maintaining the temperature of the agricultural active below its normal melting point and without contacting the active with an aromatic solvent.
(2) Description of the Related Art
Materials that affect the growth and development of agronomically important plants, or that provide some type of protection of plants from pests and diseases, are commonly referred to as agricultural actives. Such materials are widely used in modern agriculture and provide benefits of increased yield, vigor and overall plant health. However, some agricultural actives have harmful effects if they are ingested or otherwise contacted by humans or other animals.
The most common method for using agricultural actives is direct application of the active to a plant, seed, or to the soil in which the plant is to be grown. But wind, runoff and groundwater leaching can cause undesirable movement of the active, which can result in its unintended contact with plants and animals in streams, neighboring fields and homes. Furthermore, such movement of the active from the zone where protection is desired can result in reduction of the concentration of the active to below efficacious levels by the time the target pest arrives. Irreversible binding of the active to components of soil exacerbates this problem.
One method to improve the delivery and safety characteristics of agricultural actives is to include them as components of a controlled release composition. Many different types of such controlled release compositions are known and include the encapsulation of droplets, the formation of a coating on solid particles, and the inclusion of actives in matrix microparticles. Such formulations typically place coatings of a barrier material between the active and the environment through which the active must move in order to reach the environment. The rate at which such transfer takes place depends upon the type of coating, its thickness, the chemical affinity of the active for the matrix, as well as many environmental parameters, such as temperature, moisture levels, and the like.
Thus, encapsulation of an active can improve its safety and stability, its dispersibility and even distribution, its handling characteristics, as well as to control its release rate.
Although both solid particles and liquids can be enclosed in coatings, the formation of microcapsules around liquid droplets is believed to have several advantages over the coating of solid particles. For example, microcapsules formed around liquid droplets have regular spherical geometry, coatings of even thickness, and lack sharp edges and concave surfaces, which can occur in coatings of solid particles, and which could cause uneven coating thickness or even lack of a coating on some parts of the active. A coating having a regular geometry and an even thickness provides more predictable release characteristics than an uneven coating of varying thickness.
A number of methods for the encapsulation of liquid droplets containing agricultural actives is known in the art, and a summary of such methods is provided, for example, in Controlled-Release Delivery Systems for Pesticides, H. B. Scher, Ed., Marcel Dekker, Inc., New York (1999); in Microencapsulation, S. Benita, Ed., Marcel Dekker, New York (1996); and in Microencapsulation and Related Drug Processes, Patrick B. Deasy, Ed., Marcel Dekker, New York (1984).
Matson, in U.S. Pat. Nos. 3,516,846 and 3,516,941 and Sher et al., in U.S. Pat. No. 4,956,129, describe the formation of a urea-formaldehyde polymer coating around small liquid droplets.
Another commonly used method for the encapsulation of liquid droplets involves the generation of a polyurea shell around an active-containing core by interfacial polymerization at the surface of the droplets. Advantages of using a polyurea shell include that the material is generally non-phytotoxic, its permeability characteristics can be controlled, and the shell can be formed at relatively low temperatures—in fact, polymerization temperatures of lower than 90° C. are almost always used, and temperatures of from about 40° C.-70° C., are preferred.
In U.S. Pat. Nos. 4,285,720 and 4,643,764, Scher describes a process involving the blending of various pesticides with an organic polyisocyanate to form an organic phase, which is dispersed into small droplets into an aqueous phase. Some molecules of the organic polyisocyanate hydrolyze to form amines, which then can react with other isocyanates to form the polyurea shell.
Chao, in U.S. Pat. No. 4,599,271, describes the use of two or more organic-in-aqueous emulsions for the formation of a polyurea shell around a polyisocyanate containing droplet.
Beestman (in U.S. Pat. No. 4,640,709) discloses the inclusion of an alkylated polyvinyl pyrrolidone polymer that acts as an emulsifier in the aqueous phase of a two-phase system which is capable of providing microcapsules having high levels of an enclosed water-immiscible material.
In U.S. Pat. No. 4,681,806, Matkan et al. describe particles containing a releasable fill material and having a polyurea surface layer that encloses a polyurea matrix having the fill material contained therein.
Ohtsubo et al. (in U.S. Pat. No. 4,889,719) describe the microencapsulation of organophosphorous insecticidal compositions by the formation of a polyurea shell. Similar methods have been used for the microencapsulation of herbicidally active N-chloroacetylcyclohexeneamines and herbicidally active chloroacetanilide in a polyurea shell, and are described in U.S. Pat. No. 5,006,161, to Hasslin et al.
In U.S. Pat. No. 4,738,898, Vivant describes microencapsulation of a variety of materials within polyurea skin membranes by interfacial polyaddition involving a polyisocyanato hydrophobic liquid in an essentially aqueous medium. The polyisocyanato hydrophobic liquid contained the dissolved material to be encapsulated, an aliphatic diisocyanate and an isocyanurate ring trimer of an aliphatic diisocyanate. The isocyanate materials were reacted with a polyamine to form a polyurea shell material. The microcapsules described by Vivant had leakproof walls that were designed for the microencapsulation of colorants and the production of pressure-sensitive carbonless paper, for example. The microcapsules were designed to maintain the encapsulated material until the capsule was ruptured, and would not have been suitable for the controlled release of the encapsulated materials through the walls of the capsule.
Hasslin et al. (in U.S. Pat. No. 4,938,797) describes the encapsulation of a water-immiscible pesticide in a polyurea shell. The method includes the use of an anionic dispersant, such as a salt of polystyrenesulfonic acid in the aqueous phase. A similar method is described in U.S. Pat. No. 5,310,721, to Lo, but all of the agricultural active materials that are encapsulated are liquids at ambient temperature.
Seitz et al. (in U.S. Pat. No. 5,925,595) disclose a process for the preparation of microencapsulated materials—including low-melting herbicides, such as acetanilides—by combining a triisocyanate and a diisocyanate with a water immiscible composition which can include the herbicide; forming a dispersion of the core chemical and the blend of isocyanates in an aqueous liquid; and reacting the isocyanates with a polyamine to form microcapsules.
In U.S. Pat. No. 6,133,197, Chen et al., describe the formation of quick release microcapsules containing an agriculturally active material and having a polyurea shell with relatively low degree of cross-linking.
Despite the advantages provided by microcapsules having polyurea shells that enclose liquid cores containing agricultural actives, the methods that are known for the formation of these structures have certain limitations that limit their use with certain highly promising actives. For example, if the agricultural active has a melting point that is close to, or higher than, the preferred range of polymerization temperature for polyurea shell formation, it is difficult to liquify the active in order to form the microcapsule. A common solution to this situation has been to dissolve the active in an aromatic solvent. See, e.g., WO 00/27200, where the formation of a slow release capsule suspension is described wherein a mixture of a fungicide (thienol[2,3-d]pyrimidin-4-one) and another agricultural active (selected from a list of possible materials) is blended with polyisocyanates in an aromatic solvent. This organic phase is emulsified in an aqueous liquid phase, and 1,6-diaminohexane is added to cause a polymerization reaction with the isocyanates to form microcapsules that enclose the mixture of agricultural actives.
Since many aromatic solvents are phytotoxic, their use in controlled release formulations intended for application to plants or seeds would appear to be potentially harmful to the plant.
One new class of agricultural actives that appears to be very promising for fungicidal and other applications is described in U.S. Pat. Nos. 5,482,974, 5,486,621, 5,498,630, 5,693,667, 5,693,667, 5,705,513, 5,811,411, 5,834,447, 5,849,723, 5,994,270, 5,998,466, 6,028,101, and in publications WO 93/07751, and EP 0 538 231 A1. One such compound, in particular, is 4,5-dimethyl-N-(2-propenyl)-2-(trimethylsilyl)-3-thiophenecarboxamide, having a CAS registration number of 175217-20-6, and for which the proposed ISO common name is “Silthiopham”. Silthiopham has a normal melting point of about 86° C.-88° C., which has limited its incorporation into polyurea microcapsules by known techniques. Further information about silthiopham can be found in U.S. Pat. No. 5,486,621.
Accordingly, it would be useful to provide a method for the formation of microcapsules enclosing such high-melting agricultural actives where the method was free of the use of aromatic solvents—and preferably free of any solvents—and where the method could be carried out at a temperature that was below the normal melting point of the active. It would also be useful if such method allowed for the use of a polyurea shell that could be designed to release the active from the microcapsule at a controlled rate when the microcapsule was exposed to natural environmental conditions.
Briefly, therefore the present invention is directed to a novel method of producing a controlled release form of a first agricultural active having a normal melting point, the method comprising providing an organic liquid composition comprising a first agricultural active having low water solubility where the composition is free of aromatic solvents; forming the liquid composition into small droplets while maintaining said liquid composition at a temperature below the normal melting point of the first agricultural active; and enclosing each droplet in a non-water soluble shell to form a microcapsule. When desired, the shell can be designed to release the first agricultural active from the microcapsule at a pre-selected controlled rate when the microcapsule is exposed to natural environmental conditions.
The present invention is also directed to a novel controlled release form of an agricultural active comprising a compound having the formula
wherein Z1 and Z2 are C or N and are part of an aromatic ring selected from benzene, pyridine, thiophene, furan, pyrrole, pyrazole, thiazole, and isothiazole;
a) halo, formyl, cyano, amino, nitro, thiocyanato, isothiocyanato, trimethylsilyl, and hydroxy;
b) C1-C4 alkyl, alkenyl, alkynyl, C3-C6 cycloalkyl, and cycloalkenyl, each optionally substituted with halo, hydroxy, thio, amino, nitro, cyano, formyl, phenyl, C1-C4 alkoxy, alkylcarbonyl, alkylthio, alkylamino, dialkylamino, alkoxycarbonyl, (alkylthio)carbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylsulfinyl, or alkylsulfonyl;
c) phenyl, furyl, thienyl, pyrrolyl, each optionally substituted with halo, formyl, cyano, amino, nitro, C1-C4 alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylamino, dialkylamino, haloalkyl, and haloalkenyl;
d) C1-C4 alkoxy, alkenoxy, alkynoxy, C3-C6 cycloalkyloxy, cycloalkenyloxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, dialkylamino, alkylcarbonylamino, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylcarbonyl, alkylcarbonyloxy, alkoxycarbonyl, (alkylthio)carbonyl, phenylcarbonylamino, phenylamino, each optionally substituted with halo;
wherein two R groups may be combined to form a fused ring;
each R2 is independently selected from alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl and phenyl, each optionally substituted with R4 or halogen; and wherein, when Q is C, R2 may also be selected from halo, alkoxy, alkylthio, alkylamino, and dialkylamino;
wherein two R2 groups may be combined to form a cyclo group with Q;
R4 is C1-C4 alkyl, haloalkyl, alkoxy, alkylthio, alkylamino, or dialkylamino;
The present invention is also drawn to a novel method of reducing the melting point of an agricultural active material having the formula
wherein Z1 and Z2 are C or N and are part of an aromatic ring selected from benzene, pyridine, thiophene, furan, pyrrole, pyrazole, thiazole, and isothiazole;
a) halo, formyl, cyano, amino, nitro, thiocyanato, isothiocyanato, trimethylsilyl, and hydroxy;
b) C1-C4 alkyl, alkenyl, alkynyl, C3-C6 cycloalkyl, and cycloalkenyl, each optionally substituted with halo, hydroxy, thio, amino, nitro, cyano, formyl, phenyl, C1-C4 alkoxy, alkylcarbonyl, alkylthio, alkylamino, dialkylamino, alkoxycarbonyl, (alkylthio)carbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylsulfinyl, or alkylsulfonyl;
c) phenyl, furyl, thienyl, pyrrolyl, each optionally substituted with halo, formyl, cyano, amino, nitro, C1-C4 alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylamino, dialkylamino, haloalkyl, and haloalkenyl;
d) C1-C4 alkoxy, alkenoxy, alkynoxy, C3-C6 cycloalkyloxy, cycloalkenyloxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, dialkylamino, alkylcarbonylamino, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylcarbonyl, alkylcarbonyloxy, alkoxycarbonyl, (alkylthio)carbonyl, phenylcarbonylamino, phenylamino, each optionally substituted with halo;
wherein two R groups may be combined to form a fused ring;
each R2 is independently selected from alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl and phenyl, each optionally substituted with R4 or halogen; and wherein, when Q is C, R2 may also be selected from halo, alkoxy, alkylthio, alkylamino, and dialkylamino;
wherein two R2 groups may be combined to form a cyclo group with Q;
R4 is C1-C4 alkyl, haloalkyl, alkoxy, alkylthio, alkylamino, or dialkylamino;
The present invention is also directed to a novel controlled release form of an agricultural active comprising a compound having the formula
wherein Z1 and Z2 are C or N and are part of an aromatic ring selected from benzene, pyridine, thiophene, furan, pyrrole, pyrazole, thiazole, and isothiazole;
a) halo, formyl, cyano, amino, nitro, thiocyanato, isothiocyanato, trimethylsilyl, and hydroxy;
b) C1-C4 alkyl, alkenyl, alkynyl, C3-C6 cycloalkyl, and cycloalkenyl, each optionally substituted with halo, hydroxy, thio, amino, nitro, cyano, formyl, phenyl, C1-C4 alkoxy, alkylcarbonyl, alkylthio, alkylamino, dialkylamino, alkoxycarbonyl, (alkylthio)carbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylsulfinyl, or alkylsulfonyl;
c) phenyl, furyl, thienyl, pyrrolyl, each optionally substituted with halo, formyl, cyano, amino, nitro, C1-C4 alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylamino, dialkylamino, haloalkyl, and haloalkenyl;
d) C1-C4 alkoxy, alkenoxy, alkynoxy, C3-C6 cycloalkyloxy, cycloalkenyloxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, dialkylamino, alkylcarbonylamino, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylcarbonyl, alkylcarbonyloxy, alkoxycarbonyl, (alkylthio)carbonyl, phenylcarbonylamino, phenylamino, each optionally substituted with halo;
wherein two R groups may be combined to form a fused ring;
each R2 is independently selected from alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl and phenyl, each optionally substituted with R4 or halogen; and wherein, when Q is C, R2 may also be selected from halo, alkoxy, alkylthio, alkylamino, and dialkylamino;
wherein two R2 groups may be combined to form a cyclo group with Q;
R4 is C1-C4 alkyl, haloalkyl, alkoxy, alkylthio, alkylamino, or dialkylamino;
a structure which controls the release of said compound.
The present invention is also directed to a novel microcapsule comprising a polyurea shell enclosing a core which comprises silthiopham, where the microcapsule has an average size of from about 2μ to about 8μ where the weight ratio of the shell to the core is from about 15:100 to about 30:100, and where the amount of silthiopham in the core is from about 30% to about 60%, by weight.
The present invention is also directed to a novel method of producing a microencapsulated form of a high melting material which method is free of the use of solvents, the method comprising mixing a high melting material and a melting point depressant to form a composition which is free of solvents; heating the composition to a temperature at which the composition is a liquid, but which temperature is below the normal melting points of both the high melting material and the melting point depressant; forming the liquid composition into small droplets while maintaining said liquid composition at a temperature below the normal melting points of both the high melting material and the melting point depressant; and enclosing each droplet in a non-water soluble shell by interfacial polymerization to form a microcapsule.
Among the several advantages found to be achieved by the present invention, therefore, may be noted the provision of a method for the formation of microcapsules enclosing high-melting agricultural actives where the method was free of the use of aromatic solvents and where the method could be carried out at a temperature that was below the normal melting point of the active, and the provision of a method that allowed for the use of a polyurea shell that could be designed to release the active from the microcapsule at a controlled rate when the microcapsule was exposed to natural environmental conditions.
In accordance with the present invention, it has been discovered that microcapsules containing a high-melting agricultural active material (as those terms are defined below) can be produced without raising the temperature of the active to its normal melting point and without the use of an aromatic solvent. The microcapsules can have an outer shell that is formed of polyurea and the microcapsules can be designed to release the active from the microcapsule at a pre-selected controlled rate when the microcapsule is exposed to natural environmental conditions.
In one embodiment, this disclosure describes the microencapsulation of a first agricultural active, such as silthiopham, in a polyurea shell, where the encapsulation is achieved by an interfacial polymerization process. Two processes are disclosed for preparing the emulsion necessary for the interfacial polymerization, one involves encapsulation of the active in solution in a non-aromatic organic solvent and the other involves encapsulation of a blend of the active and a melting point depressant.
The embodiment of the present invention involving the production of microcapsules that contain silthiopham in the core and which are free of non-aromatic solvents, is believed to be particularly advantageous. It is believed that such microcapsules, applied to wheat seed in the fall, could provide an initial level of protection sufficient to protect the seed from harmful biological activity until temperatures fall low enough that biological pressure becomes insignificant for the winter, but would retain a sufficient amount of the active so that it would still be releasing at a sufficient level in the spring to provide protection against the increasing biological pressure throughout sprouting and initial growth of the plant. This type of protection from only one seed treatment with the novel microcapsules would provide protection for the seeds and the plants and would save at least one, and perhaps two, conventional field applications of a pesticide.
As will be discussed in detail below, it has been found that the novel microcapsules can be designed to provide a pre-selected controlled rate of release of an enclosed active, by controlling, among other parameters, the active loading in the core, the thickness of the shell wall, the particle size, and the composition of the shell wall. This ability to control the release profile permits the tailoring of the microcapsules to meet a wide range of application demands. As would be understood by one having skill in the art, the release rate of the encapsulated active material would be affected by such environmental parameters as temperature and moisture. However, one can use the controllable parameters described above to provide a desired release rate for any particular set of environmental conditions. For example, if one knew the geographic location in which the novel material was to be used, it would be possible to predict the temperature to be expected during the different seasons, and to design a material that would provide a certain release rate at the predicted temperatures.
One embodiment of the present invention advantageously extends the state of the art to include the encapsulation of almost any high melting solid by a method that includes interfacial polymerization, but without the necessity of using a solvent to dissolve the high melting solid. In U.S. Pat. No. 5,310,721, to Lo, it is taught that microcapsules prepared by interfacial polycondensation can advantageously contain materials which have a variety of uses, such as for dyes, inks, color formers, pharmaceuticals, cosmetics, flavoring materials, agricultural chemicals, and the like. The Lo patent states that any liquid, oil, low melting solid, or solvent-soluble material into which a first wall-forming material can be dissolved and which is non-reactive with said wall-forming material may be encapsulated with this technique.
The present invention extends the state of the art to include the encapsulation of almost any high melting solid by forming a mixture of the high melting solid with a melting point depressant that is a solid at conventional interfacial polymerization temperatures (for polyurea formation, this is about 50° C.-90° C.), but is capable of combining with the high melting solid to form a eutectic mixture, where the melting point of the eutectic mixture is sufficiently low to permit the mixture to be encapsulated by known interfacial polymerization techniques, such as referred to in the Lo patent. It is preferable, but not required, that the melting point depressant is a material of the same type as the high melting solid. For example, it is particularly advantageous when both are dyes, inks, pharmaceuticals, flavoring materials, agricultural chemicals, and the like.
As used herein, a “material having a high normal melting point”, which is also referred to herein as a “high melting material”, is a material which has a normal melting point temperature that is higher than the upper limit of the temperature range that is conventionally used to carry out the interfacial polymerization method that is being used to form the encapsulating shell around the material. For example, when the interfacial polymerization method comprises the formation of a polyurea shell, the preferred temperature range that is conventionally used is about 50° C. to about 90° C., more preferably, about 50° C. to about 80° C., even more preferably, about 50° C. to about 70° C., and yet more preferably, about 50° C. to about 60° C. Therefore, a high melting material, in this instance, is one having a normal melting point that is above 90° C., or above the upper limit of another of the preferred ranges.
It is preferred that the first agricultural active, the high melting material, and the melting point depressant, are materials that have a low water solubility. When it is said that such a material has a “low water solubility”, or is “non-water soluble”, it is meant that such material has a solubility in water at 25° C. of less than about 1%, by weight. It is preferred that the water solubility is less than about 0.1%, by weight, more preferred that it is less than about 0.01% by weight, yet more preferred that it is less than about 0.001% by weight, and even more preferred that it is less than about 0.0001% by weight.
When the material having a high normal melting point is an agricultural active, the terms “high-melting point agricultural active”, or “high-melting active”, as used herein, mean an agricultural active having a normal melting point that is the same as described above for a high melting material. In general, a high-melting agricultural active materials is one that is difficult to encapsulate neat by conventional methods for forming a polyurea shell around a core of the active.
The “normal melting point” of a material, as those terms are used herein, refers to the temperature at which the solid form of the material is in equilibrium with the liquid form at atmospheric pressure. It is understood that such terms include the description of materials—such as some polymers—which sometimes have a range of temperature over which melting occurs. In these cases, the normal melting point of a polymer can be understood to be any temperature within the normal melting range for the polymer; commonly it is a temperature at or near the mid-point of the melting range. For example, a material having a normal melting range of 86° C.-88° C., could be said to have a normal melting point of about 87° C.
Agricultural active materials that are suitable for use in the present invention include the compounds described in U.S. Pat. Nos. 5,482,974, 5,486,621, 5,498,630, 5,693,667, 5,693,667, 5,705,513, 5,811,411, 5,834,447, 5,849,723, 5,994,270, 5,998,466, 6,028,101, and in publications WO 93/07751, and EP 0 538 231 A1. In particular, such compounds are described in U.S. Pat. No. 5,693,667 and in European Patent Application No. 0 538 231 A1, which describe compounds having the formula
wherein Z1 and Z2 are C or N and are part of an aromatic ring selected from benzene, pyridine, thiophene, furan, pyrrole, pyrazole, thiazole, and isothiazole;
a) halo, formyl, cyano, amino, nitro, thiocyanato, isothiocyanato, trimethylsilyl, and hydroxy;
b) C1-C4 alkyl, alkenyl, alkynyl, C3-C6 cycloalkyl, and cycloalkenyl, each optionally substituted with halo, hydroxy, thio, amino, nitro, cyano, formyl, phenyl, C1-C4 alkoxy, alkylcarbonyl, alkylthio, alkylamino, dialkylamino, alkoxycarbonyl, (alkylthio)carbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylsulfinyl, or alkylsulfonyl;
c) phenyl, furyl, thienyl, pyrrolyl, each optionally substituted with halo, formyl, cyano, amino, nitro, C1-C4 alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylamino, dialkylamino, haloalkyl, and haloalkenyl;
d) C1-C4 alkoxy, alkenoxy, alkynoxy, C3-C6 cycloalkyloxy, cycloalkenyloxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, dialkylamino, alkylcarbonylamino, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylcarbonyl, alkylcarbonyloxy, alkoxycarbonyl, (alkylthio)carbonyl, phenylcarbonylamino, phenylamino, each optionally substituted with halo;
wherein two R groups may be combined to form a fused ring;
each R2 is independently selected from alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl and phenyl, each optionally substituted with R4 or halogen; and wherein, when Q is C, R2 may also be selected from halo, alkoxy, alkylthio, alkylamino, and dialkylamino;
wherein two R2 groups may be combined to form a cyclo group with Q;
R4 is C1-C4 alkyl, haloalkyl, alkoxy, alkylthio, alkylamino, or dialkylamino;
The term “amine” in —C(X)-amine means an unsubstituted, monosubstituted, or disubstituted amino radical, including nitrogen-bearing heterocycles. Examples of substituents for the amino radical include, but are not limited to, hydroxy; alkyl, alkenyl, and alkynyl, which may be straight or branched chain or cyclic; alkoxyalkyl; haloalkyl; hydroxyalkyl; alkylthio; alkylthioalkyl; alkylcarbonyl; alkoxycarbonyl; aminocarbonyl; alkylaminocarbonyl; cyanoalkyl; mono- or dialkylamino; phenyl, phenylalkyl or phenylalkenyl, each optionally substituted with one or more C1-C6 alkyl, alkoxy, haloalkyl, C3-C6 cycloalkyl, halo, or nitro groups; C1-C4 alkyl or alkenyl groups substituted with heterocycles, optionally substituted with one or more C1-C4 alkyl, alkoxy, haloalkyl, halo, or nitro groups. Examples of such nitrogen-bearing heterocycles, which are bonded at a nitrogen to —C(X)—, include, but are not limited to, morpholine, piperazine, piperidine, pyrrole, pyrrolidine, imidazole, and triazoles, each of which may be optionally substituted with one or more C1-C6 alkyl groups.
Specific examples of the amino radicals useful in the present invention include, but are not limited to, ethylamino, methylamino, propylamino, 2-methylethylamino, 1-propenylamino, 2-propenylamino, 2-methyl-2-propenylamino, 2-propynylamino, butylamino, 1,1-dimethyl-2-propynylamino, diethylamino, dimethylamino, N-(methyl)ethylamino, N-(methyl)-1,1(dimethyl)ethylamino, dipropylamino, octylamino, N-(ethyl)-1-methylethylamino, 2-hydroxyethylamino, 1-methylpropylamino, chloromethylamino, 2-chloroethylamino, 2-bromoethylamino, 3-chloropropylamino, 2,2,2-trifluoroethylamino, cyanomethyl, methylthiomethylamino, (methylsulfonyl)oxyethylamino, 2-ethoxyethylamino, 2-methoxyethylamino, N-(ethyl)-2-ethoxyethylamino, 1-methoxy-2,2-dimethylpropylamino, cyclopropylamino, cyclobutylamino, cyclopentylamino, cyclohexylamino, methoxymethylamino, N-(methoxymethyl)ethylamino, N-(1-methylethyl)propylamino, 1-methylheptylamino, N-(ethyl)-1-methylheptylamino, 6 ,6-dimethyl-2-hepten-4-ynylamino, 1,1-dimethyl-2-propynylamino. Further examples include benzylamino, ethylbenzylamino, 3-methoxybenzylamino, 3-(trifluoromethyl)benzylamino, N-methyl-3-(trifluoromethyl)benzylamino, 3,4,5-trimethoxybenzylamino, 1,3-benzodioxol-5-ylmethylamino, phenylamino, 3-(1-methylethyl)phenylamino, ethoxyphenylamino, cyclopentylphenylamino, methoxyphenylamino, nitrophenylamino, 1-phenylethylamino, N-(methyl)-3-phenyl-2-propenylamino, benzotriazolylphenylmethyl, 2-pyridinylmethylamino, N-(ethyl)-2-pyridinylmethylamino, 2-thienylmethylamino, and furylmethylamino. Further examples of amino radicals include methylhydrazino, dimethylhydrazino, N-ethylanilino, and 2-methylanilino. The amine may also be substituted with diethyl N-ethylphosphoramidic acid, t-butoxycarbonyl, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, etc. Of these examples of the amino radical, ethylamino is preferred.
Examples of B include, but are not limited to, trimethylsilyl, ethyldimethylsilyl, diethylmethylsilyl, triethylsilyl, dimethylpropylsilyl, dipropylmethylsilyl, dimethyl-1-(methyl)ethylsilyl, tripropylsilyl, butyldimethylsilyl, pentyidimethylsilyl, hexyldimethylsilyl, cyclopropyldimethylsilyl, cyclobutyldimethylsilyl, cyclopentyidimethylsilyl, cyclohexyldimethylsilyl, dimethylethenylsilyl, dimethylpropenylsilyl, chloromethyldimethylsilyl, 2-chloroethyldimethylsilyl, bromomethyldimethylsilyl, bicycloheptyldimethylsilyl, dimethylphenylsilyl, dimethyl-2-(methyl)phenylsilyl, dimethyl-2-fluorophenylsilyl, and other such silyl groups of the formula Si(R2)3; any such silyl group connected to the Z1-Z2 ring by a methylene group; and any of these groups wherein germanium or tin is substituted for silicon. Of these examples of B, trimethylsilyl is preferred.
Further examples of B include 1,1-dimethylethyl, 1,1-dimethylpropyl, 1,1-dimethylbutyl, 1,1-dimethylpentyl, 1-ethyl-1-methylbutyl, 2,2-dimethylpropyl, 2,2-dimethylbutyl, 1-methyl-1-ethylpropyl, 1,1-diethylpropyl, 1,1,2-trimethylpropyl, 1,1,2-trimethylbutyl, 1,1,2,2-tetramethylpropyl, 1,1-dimethyl-2-propenyl, 1,1,2-trimethyl-2-propenyl, 1,1-dimethyl-2-butenyl, 1,1-dimethyl-2-propynyl, 1,1-dimethyl-2-butynyl, 1-cyclopropyl-1-methylethyl, 1-cyclobutyl-1-methylethyl, 1-cyclopentyl-1-methylethyl, 1-(1-cyclopentenyl)-1-methylethyl, 1-cyclohexyl-1-methylethyl, 1-(1-cyclohexenyl)-1-methylethyl, 1-methyl-1-phenylethyl, 1,1-dimethyl-2-chloroethyl, 1,1-dimethyl-3-chloropropyl, 1,1-dimethyl-2-methoxyethyl, 1,1-dimethyl-2-(methylamino)ethyl, 1,1-dimethyl-2-(dimethylamino)ethyl, 1,1-dimethyl-3-chloro-2-propenyl, 1-methyl-1-methoxyethyl, 1-methyl-1-(methylthio)ethyl, 1-methyl-1-(methylamino)ethyl, 1-methyl-1-(dimethylamino)ethyl, 1-chloro-1-methylethyl, 1-bromo-1-methylethyl, and 1-iodo-1-methylethyl. Of these examples of B, 1,1-dimethylethyl is preferred.
Further examples of B are 1,1-dimethylethylamino, 1,1-dimethylpropylamino, 1,1-dimethylbutylamino, 1,1-dimethylpentylamino, 1-ethyl-1-methylbutylamino, 2,2-dimethylpropylamino, 2,2-dimethylbutylamino, 1-methyl-1-ethylpropylamino, 1,1-diethylpropylamino, 1,1,2-trimethylpropylamino, 1,1,2-trimethylbutylamino, 1,1,2,2-tetramethylpropylamino, 1,1-dimethyl-2-propenylamino, 1,1,2-trimethyl-2-propenylamino, 1,1-dimethyl-2-butenylamino, 1,1-dimethyl-2-propynylamino, 1,1-dimethyl-2-butynylamino, 1-cyclopropyl-1-methylethylamino, 1-cyclobutyl-1-methylethylamino, 1-cyclopentyl-1-methylethylamino, 1-(1-cyclopentenyl)-1-methylethylamino, 1-cyclohexyl-1-methylethylamino, 1-(1-cyclohexenyl)-1-methylethylamino, 1-methyl-1-phenylethylamino, 1,1-dimethyl-2-chloroethylamino, 1,1-dimethyl-3-chloropropylamino, 1,1-dimethyl-2-methoxyethylamino, 1,1-dimethyl-2-(methylamino)ethylamino, 1,1-dimethyl-2-(dimethylamino)ethylamino, and 1,1-dimethyl-3-chloro-2-propenylamino. Any of these groups may also have a methyl substitution on the nitrogen, as in N-(methyl)-1,1-dimethylethylamino and N-(methyl)-1,1-dimethylpropylamino. Of these examples of B, 1,1-dimethylethylamino and N-(methyl)-1,1-dimethylethylamino are preferred.
Further examples of B include 1,1-dimethylethoxy, 1,1-dimethylpropoxy, 1,1-dimethylbutoxy, 1,1-dimethylpentoxy, 1-ethyl-1-methylbutoxy, 2,2-dimethylpropoxy, 2,2-dimethylbutoxy, 1-methyl-1-ethylpropoxy, 1,1-diethylpropoxy, 1,1,2-trimethylpropoxy, 1,1,2-trimethylbutoxy, 1,1,2,2-tetramethylpropoxy, 1,1-dimethyl-2-propenoxy, 1,1,2-trimethyl-2-propenoxy, 1,1-dimethyl-2-butenoxy, 1,1-dimethyl-2-propynyloxy, 1,1-dimethyl-2-butynyloxy, 1-cyclopropyl-1-methylethoxy, 1-cyclobutyl-1-methylethoxy, 1-cyclopentyl-1-methylethoxy, 1-(1-cyclopentenyl)-1-methylethoxy, 1-cyclohexyl-1-methylethoxy, 1-(1-cyclohexenyl)-1-methylethoxy, 1-methyl-1-phenylethoxy, 1,1-dimethyl-2-chloroethoxy, 1,1-dimethyl-3-chloropropoxy, 1,1-dimethyl-2-methoxyethoxy, 1,1-dimethyl-2-(methylamino)ethoxy, 1,1-dimethyl-2-(dimethylamino)ethoxy, 1,1-dimethyl-3-chloro-2-propenoxy. Of these examples of B, 1,1-dimethylethoxy is preferred.
Further examples of B include 1 methylcyclopropyl, 1-methylcyclobutyl, 1-methylcyclopentyl, 1-methylcyclohexyl, 1-methylcyclopropylamino, 1-methylcyclobutylamino, 1-methylcyclopentylamino, 1-methylcyclohexylamino, N-(methyl)-1-methylcyclopropylamino, N-(methyl)-1-methylcyclobutylamino, N-(methyl)-1-methylcyclopentylamino, and N-(methyl)-1-methylcyclohexylamino.
Rn may be any substituent(s) which do(es) not unduly reduce the effectiveness of the compounds to function in the method of disease control. Rn is generally a small group; “n” is preferably 1 for benzene rings and 2 for furan and thiophene. R is more preferably methyl or halogen, and more preferably is located adjacent to A.
When Z1 and Z2 are part of a benzene ring, the following are not included as useful active agents of the present invention: 1) n is not zero when B is trimethylsilyl and A is N,N-diethylaminocarbonyl, N,N-bis(1-methylethyl)aminocarbonyl, N-methylaminothiocarbonyl, N-ethylaminocarbonyl, 1-piperidinylcarbonyl, or N-phenylaminocarbonyl; or when B is orthotolyl and A is N,N-diethylaminocarbonyl, N,N-bis(1methylethyl)aminocarbonyl, N-methylaminocarbonyl, or O-methylcarbamyl; or when B is 1,1-dimethylethyl and A is N,N-dimethylaminothiocarbonyl or N-phenylaminocarbonyl; or when B is trimethylstannyl and A is N,N-diethylaminocarbonyl or O-(1,1-dimethylethyl)carbamyl; 2) when B is 2-trimethylsilyl and A is N,N-diethylaminocarbonyl, Rn is not 3-fluoro-6-formyl, 3-fluoro-6methyl, 3-chloro-6-formyl, 3-fluoro, 3-chloro, 3-chloro-6-methyl, 6-trimethylsilyl, or 6-methyl; 3) when A is O-(1,1-dimethylethyl)carbamyl and B is 2-trimethylsilyl, Rn is not 5-trifluoromethyl; 4) when A is N-phenylaminocarbonyl and B is 2,2-dimethylpropyl, Rn is not 3-methyl; and 5) R is not isothiocyanato when A is —C(O)-amine and Wm is —O—.
When Z1 and Z2 are part of a thiophene, furan or pyrrole ring, the novel compounds of the present invention do not include B equal to trimethylsilyl when A is (diethylamino)carbonyl.
Useful agricultural actives of the type described above have also been described in U.S. Pat. No. 5,998,466 as a compound having the formula
wherein Z1 and Z2 are C or N and are part of an aromatic ring which is thiophene;
A is selected from —C(X)-amine, wherein the amine is substituted with a first and a second amine substituent or with an alkylaminocarbonyl and a hydrogen, —C(O)—SR3, —NH—C(X)R4, and —C(═NR3)—XR7;
the first amine substituent which is selected from the group consisting of C1-C10 straight or branched alkyl, alkenyl, or alkylaryl groups or mixtures thereof optionally substituted with one or more halogen, hydroxy, alkoxy, alkylthio, nitrile, alkylsulfonate, haloalkylsulfonate, phenyl, C3-C6 cyclocalkyl and C5-C6 cycloalkynel; phenyl optionally substituted with one or more C1-C4 straight or branched alkyl, alkenyl, or alkynyl groups or mixtures thereof, cycloalkyl, cycloalkenyl, haloalkyl, alkoxy and nitro; C3-C6 cycloalkyl, C5-C6 cycloalkenyl, alkoxy, alkenoxy, alkynoxy, dialkylamino, and alkylthio;
and the second amine substituent which is selected from the group consisting of hydrogen; C1-C6 straight or branched alkyl, alkenyl, or alkynyl groups or mixtures thereof optionally substituted with one or more halogen; hydroxy, alkylcarbonyl, haloalkylcarbonyl, alkoxycarbonyl, and dialkylcarbonyl;
B is —Wm-Q(R2)3 or selected from o-tolyl, 1-naphthyl, 2-naphthyl, and 9-phenanthryl, each optionally substituted with halogen or R4;
Q is C, Si, Ge, or Sn;
W is —C(R3)pH(2-p)—; or when Q is C, W is selected from —C(R3)pH(2-p)—, —N(R3)mH(1-m)—, —S(O)p—, and —O—;
X is O or S;
n is 2;
m is 0 or 1;
p is 0, 1, or 2;
wherein two R groups are combined to form a nonheterocyclic ring fused with the thiophene ring, which is not a benzothiophene other than a tetrahydrobenzothiophene, said two R groups being selected from the group consisting of C1-C4 alkyl, alkenyl, C3-C6 cycloalkyl and cycloalkenyl, each optionally substituted with hydroxy, thio, phenyl, C1-C4 alkoxy, alkylthio, alkylsulfinyl, or alkylsulfonyl;
each R2 is independently selected from alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl and phenyl, each optionally substituted with R4 or halogen; and wherein, when Q is C, R2 may also be selected from halo, alkoxy, alkylthio, alkylamino, and dialkylamino; and further when Q is C, then two R2 groups may be combined to form a cycloalkyl group with Q;
R3 is C1-C4 alkyl;
R4 is C1-C4 alkyl, haloalkyl, alkoxy, alkylthio, alkylamino, or dialkylamino; and
R7 is C1-C4 alkyl, haloalkyl, or phenyl optionally substituted with halo, nitro, or R4;
or an agronomic salt thereof.
The terms “amine”, “alkyl”, “alkoxy”, “alkoxyalkyl”, “monoalkylamino”, “dialkylamino”, “haloalkyl”, and “halo”, and B, Rn, and the features of Z1 and Z2, are as described above.
Agricultural actives that are useful in the present invention can also be selected from those described in U.S. Pat. No. 5,482,974, namely, a compound having the formula
wherein R2 is ethyl, iso-propyl, propyl or allyl;
A is N(CH3)1-nHnR5 or OR6 wherein n is 0 or 1, R5 is (CH3)m(CH3CH2)3-mC, 1-methyl-1-cyclopentyl, 1-methyl-1-cyclohexyl or 2, 3-dimethyl-2-butyl wherein m is 0, 1, 2 or 3 and R6 is independently R5, or 2,3,3-trimethyl-2-butyl;
R3 is H or independently R4; and
R4 is halo or CH3;
with the proviso that when A is N(CH3)1-nHnR5, if R3 is H and R5 is 1-methyl-1-cyclohexyl or (CH3)m(CH2CH3)3-mC, where m is 0 or 3, or if R3 is halo and R2 is (CH3)m(CH3CH2)3-mC, where m is 3, then R2 cannot be ethyl;
and with the proviso that when A is OR6 then m is equal to or less than 2, and if R3 is H or halo and R2 is ethyl or isopropyl, then R6 is (CH3)M(CH3CH2)3-MC where m is 1;or an agronomic salt thereof.
Active agents that are useful in the present invention can also be selected from those described in U.S. Pat. No. 5,994,270, namely, a compound having the formula
where A is —C(X)-amine; B is —Wm-Q(R2)3; and A can be B when B is A except when the formula is f), then Q cannot be Si;
Q is C or Si;
W is —NH—, —O—or NCH3;
X is O or S;
m is 0 or 1, provided that m is 0 when Q is Si;
n is 0, 1, 2, or 3
p is 0, 1 or 2, and n plus p is equal to or less than 3; each R is independently selected from
a) halo, formyl, cyano, amino, nitro, thiocyanato, isothiocyanato, trimethylsilyl, and hydroxy;
b) C1-C4 alkyl, alkenyl, alkynyl, C3-C6 cycloalkyl, and cycloalkenyl, each optionally substituted with halo, hydroxy, thio, amino, nitro, cyano, formyl, phenyl, C1-C4 alkoxy, alkylcarbonyl, alkylthio, alkylamino, dialkylamino, alkoxycarbonyl, (alkylthio)carbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylsulfinyl, or alkylsulfonyl;
c) phenyl, furyl, thienyl, pyrrolyl, each optionally substituted with halo, formyl, cyano, amino, nitro, C1-C4 alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylamino, dialkylamino, haloalkyl, and haloalkenyl;
d) C1-C4 alkoxy, alkenoxy, alkynoxy, C3-C6 cycloalkyloxy, cycloalkenyloxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, dialkylamino, alkylcarbonylamino, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylcarbonyl, alkylcarbonyloxy, alkoxycarbonyl, (alkylthio)carbonyl, phenylcarbonylamino, phenylamino, each optionally substituted with halo; each R2 is independently selected from alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl and phenyl, each optionally substituted with R4 or halogen; and wherein, when Q is C, R2 may also be selected from halo, alkoxy, alkylthio, alkylamino, and dialkylamino; wherein two R2 groups may be combined to form a cyclo group with Q; R4 is C1-C4 alkyl, haloalkyl, alkoxy, alkylthio, alkylamino, or dialkylamino; or an agronomic salt thereof.
The term “amine” in —C(X)-amine means an unsubstituted, monosubstituted, or disubstituted amino radical, including nitrogen-bearing heterocycles. Examples of substituents for the amino radical include, but are not limited to, hydroxy; alkyl, alkenyl, and alkynyl, which may be straight or branched chain or cyclic; alkoxyalkyl; haloalkyl; hydroxyalkyl; alkylthio; alkylthioalkyl; alkylcarbonyl; alkoxycarbonyl; aminocarbonyl; alkylaminocarbonyl; cyanoalkyl; mono- or dialkylamino; phenyl, phenylalkyl or phenylalkenyl, each optionally substituted with one or more C1-C6 alkyl, alkoxy, haloalkyl, C3-C6 cycloalkyl, halo, or nitro groups; C1-C4 alkyl or alkenyl groups substituted with heterocycles, optionally substituted with one or more C1-C4 alkyl, alkoxy, haloalkyl, halo, or nitro groups. Examples of such nitrogen-bearing heterocycles, which are bonded at a nitrogen to —C(X)—, include, but are not limited to, morpholine, piperazine, piperidine, pyrrole, pyrrolidine, imidazole, and triazoles, each of which may be optionally substituted with one or more C1-C6 alkyl groups.
Specific examples of the amino radicals useful in the present invention include, but are not limited to, ethylamino, methylamino, propylamino, 2-methylethylamino, 1-propenylamino, 2-propenylamino, 2-methyl-2-propenylamino, 2-propynylamino, butylamino, 1,1-dimethyl-2-propynylamino, diethylamino, dimethylamino, N-(methyl)ethylamino, N-(methyl)-1,1-(dimethyl) ethylamino, dipropylamino, octylamino, N-(ethyl)-1-methylethylamino, 2-hydroxyethylamino, 1-methylpropylamino, chloromethylamino, 2-chloroethylamino, 2-bromoethylamino, 3-chloropropylamino, 2,2,2-trifluoroethylamino, cyanomethyl, methylthiomethylamino, (methylsulfonyl)oxyethylamino, 2-ethoxyethylamino, 2-methoxyethylamino, N-(ethyl)-2-ethoxyethylamino, 1-methoxy-2,2-dimethylpropylamino, cyclopropylamino, cyclobutylamino, cyclopentylamino, cyclohexylamino, methoxymethylamino, N-(methoxymethyl)ethylamino, N-(1-methylethyl)propylamino, 1-methylheptylamino, N-(ethyl)-1-methylheptylamino, 6,6-dimethyl-2-hepten-4-ynylamino, 1,1-dimethyl-2-propynylamino. Further examples include benzylamino, ethylbenzylamino, 3-methoxybenzylamino, 3-(trifluoromethyl)benzylamino, N-methyl-3-(trifluoromethyl)benzylamino, 3,4,5-trimethoxybenzylamino, 1,3-benzodioxol-5-ylmethylamino, phenylamino, 3-(1-methylethyl)phenylamino, ethoxyphenylamino, cyclopentylphenylamino, methoxyphenylamino, nitrophenylamino, 1-phenylethylamino, N-(methyl)-3-phenyl-2-propenylamino, benzotriazolylphenylmethyl, 2-pyridinylmethylamino, N-(ethyl)-2-pyridinylmethylamino, 2-thienylmethylamino, and furylmethylamino.
Further examples of amino radicals include methylhydrazino, dimethylhydrazino, N-ethylanilino, and 2-methylanilino. The amine may also be substituted with diethyl N-ethylphosphoramidic acid, t-butoxycarbonyl, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, etc. Of these examples of the amino radical, ethylamino, propylamino, or allylamino is preferred.
Examples of B include, but are not limited to, trimethylsilyl, ethyldimethylsilyl, diethylmethylsilyl, triethylsilyl, dimethylpropylsilyl, dipropylmethylsilyl, dimethyl-1-(methyl)ethylsilyl, tripropylsilyl, butyldimethylsilyl, pentyidimethylsilyl, hexyldimethylsilyl, cyclopropyldimethylsilyl, cyclobutyldimethylsilyl, cyclopentyidimethylsilyl, cyclohexyldimethylsilyl, dimethylethenylsilyl, dimethylpropenylsilyl, chloromethyldimethylsilyl, 2-chloroethyldimethylsilyl, bromomethyldimethylsilyl, bicycloheptyldimethylsilyl, dimethylphenylsilyl, dimethyl-2-(methyl)phenylsilyl, dimethyl-2-fluorophenylsilyl, and other such silyl groups of the formula Si(R2)3. Of these examples of B, trimethylsilyl is preferred.
Further examples of B include 1,1-dimethylethyl, 1,1-dimethylpropyl, 1,1-dimethylbutyl, 1,1-dimethylpentyl, 1-ethyl-1-methyl butyl, 2,2-dimethyl propyl, 2,2-dimethylbutyl, 1-methyl-1-ethylpropyl, 1,1-diethylpropyl, 1,1,2-trimethylpropyl, 1,1,2-trimethylbutyl, 1,1,2,2-tetramethylpropyl, 1,1-dimethyl-2-propenyl, 1,1,2-trimethyl-2-propenyl, 1,1-dimethyl-2-butenyl, 1,1-dimethyl-2-propynyl, 1,1-dimethyl-2-butynyl, 1-cyclopropyl-1-methylethyl, 1-cyclobutyl-1-methylethyl, 1-cyclopentyl-1-methylethyl, 1-(1-cyclopentenyl)-1-methylethyl, 1-cyclohexyl-1-methylethyl, 1-(1-cyclohexenyl)-1-methylethyl, 1-methyl-1-phenylethyl, 1,1-dimethyl-2-chloroethyl, 1,1-dimethyl-3-chloropropyl, 1,1-dimethyl-2-methoxyethyl, 1,1-dimethyl-2-(methylamino)ethyl, 1,1-dimethyl-2-(dimethylamino)ethyl, 1,1-dimethyl-3-chloro-2-propenyl, 1-methyl-1-methoxyethyl, 1-methyl-1-(methylthio)ethyl, 1-methyl-1-(methylamino)ethyl, 1-methyl-1-(dimethylamino)ethyl, 1-chloro-1-methylethyl, 1-bromo-1-methylethyl, and 1-iodo-1-methylethyl. Of these examples of B, 1,1-dimethylpropyl, 1,1-diethylethyl or 1-methyl-1-cyclopentyl is preferred.
Further examples of B are 1,1-dimethylethylamino, 1,1-dimethylpropylamino, 1,1-dimethylbutylamino, 1,1-dimethylpentylamino, 1-ethyl-1-methylbutylamino, 2,2-dimethylpropylamino, 2,2-dimethylbutylamino, 1-methyl-1-ethylpropylamino, 1,1-diethylpropylamino, 1,1,2-trimethylpropylamino, 1,1,2-trimethylbutylamino, 1,1,2,2-tetramethylpropylamino, 1,1-dimethyl-2-propenylamino, 1,1,2-trimethyl-2-propenylamino, 1,1-dimethyl-2-butenylamino, 1,1-dimethyl-2-propynylamino, 1,1-dimethyl-2-butynylamino, 1-cyclopropyl-1-methylethylamino, 1-cyclobutyl-1-methylethylamino, 1-cyclopentyl-1-methylethylamino, 1-(1-cyclopentenyl)-1-methylethylamino, 1-cyclohexyl-1-methylethylamino, 1-(1-cyclohexenyl)-1-methylethylamino, 1-methyl-1-phenylethylamino, 1,1-dimethyl-2-chloroethylamino, 1,1-dimethyl-3-chloropropylamino, 1,1-dimethyl-2-methoxyethylamino, 1,1-dimethyl-2-(methylamino)-ethylamino, 1,1-dimethyl-2-(dimethylamino)ethylamino, and 1,1-dimethyl-3-chloro-2-propenylamino. Of these examples of B, 1,1-dimethylpropylamino, 1,1-ethylethylamino or 1-methyl-1-cyclopentylamino is preferred.
Further examples of B include 1,1-dimethylethoxy, 1,1-dimethylpropoxy, 1,1-dimethylbutoxy, 1,1-dimethylpentoxy, 1-ethyl-1-methylbutoxy, 2,2-dimethylpropoxy, 2,2-dimethylbutoxy, 1-methyl-1-ethylpropoxy, 1,1-diethylpropoxy, 1,1,2-trimethylpropoxy, 1,1,2-trimethylbutoxy, 1,1,2,2-tetramethylpropoxy, 1,1-dimethyl-2-propenoxy, 1,1,2-trimethyl-2-propenoxy, 1,1-dimethyl-2-butenoxy, 1,1-dimethyl-2-propynyloxy, 1,1-dimethyl-2-butynyloxy, 1-cyclopropyl-1-methylethoxy, 1-cyclobutyl-1-methylethoxy, 1-cyclopentyl-1-methylethoxy, 1-(1-cyclopentenyl)-1-methylethoxy, 1-cyclohexyl-1-methylethoxy, 1-(1-cyclohexenyl)-1-methylethoxy, 1-methyl-1-phenylethoxy, 1,1-dimethyl-2-chloroethoxy, 1,1-dimethyl-3-chloropropoxy, 1,1-dimethyl-2-methoxyethoxy, 1,1-dimethyl-2-(methylamino)ethoxy, 1,1-dimethyl-2-(dimethylamino)ethoxy, 1,1-dimethyl-3-chloro-2-propenoxy. Of these examples of B, 1,1-dimethylpropyloxy, 1,1-diethylethyloxy or cyclopentyloxy is preferred.
Further examples of B include 1-methylcyclopropyl, 1-methylcyclobutyl, 1-methylcyclopentyl, 1-methyl-cyclohexyl, 1-methylcyclopropylamino, 1-methyl-cyclobutylamino, 1-methylcyclopentylamino, and 1-methyl-cyclohexylamino.
Rn may be any substituent(s) which do(es) not unduly reduce the effectiveness of the compounds to function in the method of control of Gaeumannomyces graminis var. tritici. Rn is generally a small group; “n” is preferably 0 or 1. R is preferably methyl or halogen.
As used to describe the compounds discussed just above, the term “alkyl”, unless otherwise indicated, means an alkyl radical, straight or branched chain, having, unless otherwise indicated, from 1 to 10 carbon atoms. The terms “alkenyl” and “alkynyl” mean unsaturated radicals having from 2 to 7 carbon atoms. Examples of such alkenyl groups include ethenyl, 1-propenyl, 2-propenyl, 1-butenyl, 2-butenyl, 3-butenyl, 2-methyl-1-propenyl, 2-methyl-2-propenyl, 1-methylethenyl, and the like. Examples of such alkynyl groups include ethynyl, 1-propynyl, 2-propynyl, 1,1-dimethyl-2-propynyl, and so forth. Substituent groups may also be both alkenyl and alkynyl, for example, 6,6-dimethyl-2-hepten-4-ynyl.
As used to describe the compounds discussed just above, the term “alkoxy” means an alkyl group having, unless otherwise indicated, from 1 to 10 carbon atoms connected via an ether linkage. Examples of such alkoxy groups include methoxy, ethoxy, propoxy, 1-methylethoxy, and so forth.
As used to describe the compounds discussed just above, the term “alkoxyalkyl” means an ether radical having, unless otherwise indicated, from 1 to 10 carbon atoms. Examples of such alkoxyalkyl groups include methoxymethyl, methoxyethyl, ethoxymethyl, ethoxyethyl, and so forth.
As used to describe the compounds discussed just above, the terms “monoalkylamino” and “dialkylamino” each mean an amino group having, respectively, 1 or 2 hydrogens replaced with an alkyl group.
As used to describe the compounds discussed just above, the term “haloalkyl” means an alkyl radical having one or more hydrogen atoms replaced by halogens, including radicals having all hydrogen atoms substituted by halogen. Examples of such haloalkyl groups are fluoromethyl, difluoromethyl, trifluoromethyl, chloromethyl, trichloromethyl, and so forth.
As used to describe the compounds discussed just above, the term “halo” means a radical selected from chloro, bromo, fluoro, and iodo.
A preferred active agent is a compound having the structure
and which is known as 4,5-dimethyl-N-(2-propenyl)-2-(trimethylsilyl)-3-thiophenecarboxamide, having a CAS registration number of 175217-20-6, and for which the proposed ISO common name is “Silthiopham”, or “Sylthiopham”. In this specification, this active agent may be referred to as silthiopham.
In this specification, the agricultural actives that are described above can be referred to as a “first agricultural active”. In another embodiment, the first agricultural active can include simeconazole.
The first agricultural active material of the present invention can be used in any purity that passes for such material in the commercial trade. The material can be used in any form in which it is received from the supplier, or in which it is synthesized. However, if a solvent is present, such solvents are non-aromatic organic liquid solvents that are among those that are described herein below.
When the first agricultural active is mixed with a solvent in order to form an organic phase that is a liquid at temperatures lower than the normal melting point of the first agricultural active, the solvent can be a non-aromatic organic liquid in which the active is soluble in a amount of at least about 5%, by weight, at 70° C. Preferably, the solvent is one in which the active is soluble in an amount of at least about 20%, by weight, more preferably at least about 40%, by weight, even more preferably at least about 50%, by weight, and yet more preferably at least about 60%, by weight, all at a temperature of 70° C.
It is preferred that the solvent has a normal boiling point that is higher than the upper level of the normal range of temperature that is commonly used for the polymerization reaction of the encapsulation method that is being used. A boiling point of at least about 20° C. above this upper level is preferred, at least about 30° C. above this upper level is even more preferred, and at least about 50° C. above this upper level is yet more preferred.
Suitable solvents for the present method can be found in Organic Solvents Physical Properties and Method of Purification, by Riddick, J. A., W. B. Bunger and T. K. Sakano, John Wiley & Sons, New York (1984) and can be selected from hydrocarbons, hydroxy compounds (but excluding alcohols that react more rapidly with the isocyanates that are used in the synthesis of the shell material than such isocyanates react with the amines that are used), ethers, carbonyls, acids, esters, halogenated hydrocarbons, polychlorinated hydrocarbons, brominated hydrocarbons, iodinated hydrocarbons, mixed halogenated hydrocarbons, nitro compounds, amides, sulfides, thioethers, oxo-sulfur compounds, and compounds having more than one type of characteristic atom or group. It is preferred that the solvent for use in the present method be selected from hydrocarbons, hydroxycompounds, ethers, carbonyls, esters and compounds with more than one type of characteristic atom or group.
When the solvent is a hydrocarbon, saturated aliphatic hydrocarbons such as, for example, decane, octane and dodecane, and unsaturated hydrocarbons (excluding those having an aromatic group) and including, for example, i-dodecane, 2-pinene, camphene, limonene, and the like, are useful.
Examples of hydroxy compounds that are useful include aliphatic alcohols that are not water soluble, such as cyclohexanol, 1-octanol, and the like.
Examples of ethers that are useful include aliphatic ethers that are not water soluble, such as dibutyl ether and the like.
Examples of carbonyls include camphor and the like.
Examples of esters include butyl acetate, glyceryl triacetate, butyl stearate, hexyl acetate, acetyltri-n-butyl citrate and diethyl adipate, and the like. A preferred solvent is acetyltri-n-butyl citrate (which is available under the trade name Citroflex A-4, from Morflex, Inc., Greensboro, N.C.).
When the liquid composition that contains the first agricultural active is formed by mixing the active with a solvent, it is preferred that the mixture contains at least about 5% by weight of the active, more preferred is about 25%, and even more preferred is about 50% by weight of the active. It is usually desirable to accommodate as much of the active ingredient in the core material as possible in order to extend the useful life of the microcapsules in normal use, however, as will be discussed below, it is sometimes necessary to provide the active at a level that is lower than the maximum amount possible in order to obtain the release rate characteristics that are desired.
When the active material is silthiopham, it is generally preferred to have from about 5% to about 90% by weight of silthiopham in the core, from about 10% to about 80% by weight is more preferred, from 20% to about 70% is yet more preferred, and from about 30% to about 60% by weight is even more preferred in order to obtain a desirable combination of release rate and duration of release.
When the first agricultural active is mixed with a solvent in order to form the liquid composition that will form the core of the microparticles, other agricultural actives—in addition to the first active—can also be added to the mixture. The second, or subsequent, agricultural active can be almost any agricultural active, but is preferably a pesticide or herbicide. The second active is more preferably an insecticide, acaracide, bactericide, fungicide, nematocide or molluscicide. When the second active is a fungicide, it is preferably selected from a group consisting of tebuconazole, tetraconazole, simeconazole, difenoconazole, fluquinconazole, fludioxonil, captan, metalaxyl, carboxin, and thiram.
When the second, or subsquent, agricultural active is a herbicide, it can be selected from the following useful herbicides:
growth regulators, including
phenoxy acetic acids, such as, 2,4-D and MCPA,
phenoxy propionic acids, such as, dichlorprop and mecoprop,
phenoxy butyric acids, such as, 2,4-DB and MCPB,
benzoic acids, such as, dicamba,
picolinic acid and related compounds, such as, picloram, triclopyr, clopyralid and quinclorac;
inhibitors of auxin transport, including
naptalam,
semicarbones, such as, diflufenzopyr-sodium,
s-triazines, such as, atrazine, simazine, cyanazine, prometon, ametryn and prometryn,
other triazines, such as, hexazinone and metribuzin,
substituted ureas, such as, diuron, fluometuron, linuron and tebuthiuron,
uracils, such as, bromacil and terbacil,
benzothiadiazoles, such as, bentazon,
benzonitroles, such as, bromoxymil,
phenylcarbamates, such as, desmediphram and phenmedipham,
pyridazinones, such as, pyrazon,
phenypyriddazines, such as, pyridate, and
others, such as, propanil;
pigment inhibitors, including
amitrole, clomazone and fluridone,
pyridazinones, such as, norflurazon,
isoxazoles, such as, isoxaflutole;
growth inhibitors, including
mitotic disruptors, of the types,
dinitroanilines, such as, benefin, ethalfluralin, oryzalin, pendimethalin, prodiamine and trifluralin,
oxysulfurons, such as, fluthiamide,
pyridines, such as, dithiopyr and thiazopyr,
amides, such as, pronamide, and
others, such as, DCPA;
inhibitors of shoots of emerging seedlings, of the types,
carbamothioates, such as, EPTC, cycloate, pebulate, triallate, butylate, molinate, thiobencarb and bernolate;
inhibitors of roots only of seedlings, of the types,
amides, such as, napropamide,
phenylureas, such as, siduron, and
others, such as bensulide, betasan and bensumec;
inhibitors of roots and shoots of seedlings, of the types,
chloroacetamides, such as, acetochlor, dimetenamid, propachlor, alachlor and metolachlor;
inhibitors of amino acid synthesis, including,
inhibitors of aromatic amino acid synthesis, such as, glyphosate and sulfosate,
inhibitors of branched chain amino acid synthesis, of the types,
sulfonylureas, such as, bensulfuron, chlorsulfuron, halosulfuron, nicosulfuron, prosulfuron, fimsulfuron, thifensulfuron, tribenuron, chlorimuron, ethametsulfuron, metsulfuron, primisulfuron, oxasulfuron, sulfometuron, triasulfuron and triflusulfuron,
imidazolinones, such as, imazamethabenz, imazamox, imazapic, imazapyr, imazaquin and imazethapyr,
triazolopyrimidines, such as, chloransulam and flumetsulam,
tyrimidinyloxybenzoates, such as, pyrithiobac;
lipid biosynthesis inhibitors, including,
aryoxyphenoxyproprionates, such as, ciclofop-methyl, fenoxaprop-ethyl, fenoxaprop-p-ethyl, fluazifop-p-butyl, haloxyfop and quizalofop-p-ethyl,
cyclohexanediones, such as, clethodim, sethoxydim and tralkoxydim;
inhibitors of cell wall biosynthesis, including,
nitriles, such as, dichlobenil,
benzamides, such as, isoxaben, and
others, such as, quinclorac;
cell membrane disrupters, including,
dilute sulfuric acid, monocarbamide dihydrogen sulfate and herbicidal oils,
bipyridyliums, such as, diquat and paraquat,
diphenylethers, such as, acifluorfen, fomesafen, lactofen and oxyfluorfen,
oxidiazoles, such as, fluthiacet and oxadiazon,
N-phenylheterocycles, such as carfentrazone, flumiclorac and sulfentrazone;
inhibitors of glutamine synthetase, such as glufosinate; and
others, such as, DSMA, MSMA, asulam, endothall, ethofumesate, difenzoquat and TCA.
An alternative method for providing the liquid composition containing the agricultural active comprises intermixing the first agricultural active with a melting point depressant in order to form an organic phase that is a liquid at temperatures below the normal melting point of the active. A melting point depressant of the present invention is a material that, when intermixed with the first agricultural active, is capable of forming a eutectic mixture having a melting point that is lower than the melting point of both the first agricultural active and the melting point depressant. It is preferred that the melting point depressant is one that has a normal melting point that is above normal ambient temperature. As used herein, a “eutectic mixture” is a mixture of two or more materials having the lowest melting point that is obtainable by varying the proportions of the components.
The inventors have found that, surprisingly, certain agricultural active materials, other than the first agricultural actives described above, can act as the melting point depressant of the present method. In this specification any agricultural active, other than the first agricultural actives that are described above, can be referred to as a second agricultural active. When a second agricultural active acts as a melting point depressant, such active can be a pesticide or herbicide, and can be selected from insecticides, acaricides, bactericides, fungicides, nematocides, molluscicides, and the like.
When a fungicide is used as the melting point depressant, such fungicides as tebuconazole, simeconazole, fludioxonil, fluquinconazole, difenoconazole, 4,5-dimethyl-N-(2-propenyl)-2-(trimethylsilyl)-3-thiophenecarboxamide (sylthiopham), hexaconazole, etaconazole, propiconazole, triticonazole, flutriafol, epoxiconazole, fenbuconazole, bromuconazole, penconazole, imazalil, tetraconazole, flusilazole, metconazole, diniconazole, myclobutanil, triadimenol, bitertanol, pyremethanil, cyprodinil, tridemorph, fenpropimorph, kresoxim-methyl, azoxystrobin, ZEN90160, fenpiclonil, benalaxyl, furalaxyl, metalaxyl, R-metalaxyl, orfurace, oxadixyl, carboxin, prochloraz, trifulmizole, pyrifenox, acibenzolar-S-methyl, chlorothalonil, cymoaxnil, dimethomorph, famoxadone, quinoxyfen, fenpropidine, spiroxamine, triazoxide, BAS50001F, hymexazole, pencycuron, fenamidone, guazatine, and cyproconazole, are suitable for use. Fungicides such as tebuconazole, simeconazole, difenoconazole, tetraconazole, fluquinconazole, fludioxonil, captan, metalaxyl, carboxin and thiram, are preferred.
When a herbicide is used as the melting point depressant, the herbicide can be selected from the list of herbicides that are described above as being appropriate for use as a second or subsequent agricultural active.
In one preferred embodiment of the present method the liquid composition includes silthiopham as a first agricultural active and the silthiopham is intermixed with a second agricultural active that results in the formation of a mixture having a melting point that is at least about 5° C. lower than the melting point of silthiopham. It is more preferred that the melting point of the mixture be at least about 10° C., even more preferred at least about 15° C., and yet more preferred that it be at least about 20° C. lower than the melting point of silthiopham.
Tebuconazole and simeconazole have been found to be preferred melting point depressants. A mixture of silthiopham and tebuconazole has been found to be a eutectic mixture having a eutectic point at a temperature of about 60° C., which is significantly lower than the melting point of either silthiopham (m.p. about 86° C.-88° C.) or tebuconazole (m.p. about 105° C.). For further information about the physical properties of pesticides, see, e.g., The Pesticide Manual, 11th Ed., C. D. S. Tomlin, Ed., British Crop Protection Council, Farnham, Surry, UK (1997).
After the liquid composition that contains the agricultural actives is formed by using a non-aromatic solvent, or by using a melting point depressant, as described above, the composition is dispersed into small droplets. As used herein, the term “small droplets” means droplets having an average size of less than about 20%. Although any method may be used for dispersing the liquid composition into droplets, a commonly used method is to mix the organic liquid composition with a sufficient amount of an aqueous liquid to form a continuous phase, and to carry out the mixing at high rates of shear, such as may be applied by a high shear mixer or blender.
When the small droplets of the liquid composition are formed, it has been found that the size of the droplets is a function of the rate of shear that is applied to the liquids during mixing, the viscosity of the two liquid phases, and the presence, type and amount of a surfactant or emulsifier material.
Surfactant or emulsifier materials that have been found to be useful in the present method include Lomar D (a sodium salt of naphthalene sulfonic acid polymer, 81% (CAS No. 9084-06-4) sodium sulfate, 12.5%, and water, 6.5%; available from Cognis Corp.) and Sokolan CP 9 (sodium salt of maleic acid-olefin copolymer (CAS No. 127123-37-3) available from BASF, Parsippany, N.J.).
A preferred method of forming the shell that encloses the small liquid droplets is by an interfacial polymerization of monomers to form a polyurea shell around each droplet. A method for accomplishing this polymerization is to add one or more types of isocyanate monomers to the organic liquid composition. The organic liquid composition can then be dispersed in the aqueous phase. One or more polyamine monomers can then be added to the aqueous liquid in which the organic liquid composition is dispersed. The polyamines react with the isocyanates at the interfacial surface of the small droplets (the organic/aqueous interface) to form a solid polyurea shell that encloses the droplets.
The isocyanates that are useful in the present method include polyisocyanates that can react with polyamines to form polyurea. One or more polyisocyanates can be used. Polyisocyanates that are useful in the present invention are discussed in Chemistry and Technology of Isocyanates, Ulrich, H., John Wiley & Sons, New York, (1996).
Monomeric polyisocyanates include aliphatic, cycloaliphatic, araliphatic, aromatic, and heterocyclic polyisocyanates. Examples of such polyisocyanates include 1,12-dodecane diisocyanate cyclobutane-1,3-diisocyanate, cyclohexane-1,3-diisocyanate, 2,4- and/or 2,6-hexahydrotoluylene diisocyanate, 4,4′,4″-triphenylmethane triisocyanate, tris-(4-isocyanatophenyl)-thiophosphate, Desmodur N3300 with a CA registration No: 104559-01-5, (1,6-diisocyanate homo-polymer, available from Bayer Corporation, Pittsburgh, Pa.),
It is preferred that the one or more polyisocyanates include at least one diisocyanate (having two reactive isocyanate groups per molecule) and/or at least one triisocyanate (having three reactive isocyanate groups per molecule).
Examples of useful diisocyanates can be found in the text by Ulrich, Id. at pp. 319, 330, 370, 374, and include (with commercial suppliers) HDI (Bayer), 1,5 Diisocyanatopentane, TMDI (Hüls), C12DI (duPont), 1,6,11-Undecanetriioscyanate (duPont), CHDI (Akzo), BDI (Eastman/Sun), HXDI (Takeda), IPDI (BASF, Bayer, Hüls, Olin), IMCI, DDI-1410 (Henkel), XDI (Takeda), m-TMXDI (American Cyanamid), p-TMXDI (American Cyanamid), DEBI, HMDI (Bayer), OCN(CH2)3O(CH2)3NCO, OCN(CH2)3OCH2CH2O(CH2)3NCO, OCN(CH2)3OCH(CH3)CH2O(CH2)3NCO, OCN(CH2)3O(CH2)3O(CH2)3NCO, OCN(CH2)3O(CH2)2O(CH2)2O(CH2)3NCO, OCN(CH2)3OCH(CH3)CH(CH3)O(CH2)3NCO, OCN(CH2)3OCH2C(CH3)2CH2O(CH2)3NCO, OCN(CH2)3OCH2C(Et)2CH2O(CH2)3NCO,
OCN(CH2)3O(CH2)4O(CH2)3NCO, OCN(CH2)3O(CH2)6O(CH2)3NCO, OCN(CH2)3O(CH2)10O(CH2)3NCO, PPDI (Akzo, duPont), 2,4-TDI (Bayer), TDI(80:20) (BASF, Dow, Olin, Rhone-Poulenc, Enichem), MDI (BASF, Bayer, Dow, ICI, Enichem, Mitsui, Toatsu), PMDI (BASF, Bayer, Dow, ICI, Enichem, Mitsui, Toatsu), NDI (Bayer), TODI (Nippon-Soda), and the like.
Blends of of diisocyanates and triisocyanates that are useful in the present invention are disclosed in U.S. Pat. No. 5,925,595, to Seitz et al. A preferred diisocyanate is meta-tetramethylenexylylene diisocyanate (TMXDI), and a preferred triisocyanate is N,N′,N″-tris(6-isocyanatohexyl)-nitrodotricarbonic triamide (CAS N. 67635-83-0; available as Desmodur N3,200 from Bayer Corporation, Pittsburgh, Pa.). It is more preferred that the polyisocyanates include both a diisocyanate and a triisocyanate.
It is believed that the ratio between the number of functional groups supplied by the diisocyanate and by the triisocyanate has an effect upon the composition of the polyurea shell and, thus, can be used as a controllable parameter for obtaining a desired release rate. When TMXDI and N,N′,N″-tris(6-isocyanatohexyl)-nitrodotricarbonic triamide are used as the diisocyanate and triisocyanate, respectively, a preferred ratio is 1:1.
Polyamines (i.e., polyfunctional amines) that are useful in the present method include any polyamine that is capable of reacting with polyisocyanates to form polyurea. Suitable amines include, but are not limited to, diethylene triamine, triethylene tetramine, tetraethylene pentamine, iminobispropylamines, amine epoxy adducts, alkyldiamines from ethylene diamine to hexamethylene diamine, trimethylolpropane tris[poly(propylene glycol)amine terminated]ether (available as Jeffamine T-403, CAS No. 39423-51-3) from Texaco Corp. or Aldrich), all diamines and triamines produced by Texaco Corp. and marketed under the trade name of Jeffamine, piperazine, isophorone diamine, bis-(4-aminocyclohexyl)methane, 1,2-, 1,3-, and 1,4-cyclohexane diamine, 1,2-propane diamine, N,N,N-tris-(2-aminoethyl)-amine, poly(ethyleneimine)s, N-(2-aminoethyl)-piperazine, N,N′-bis-(3-aminopropyl)-ethylenediamine, N,N′-bis-(2-aminoethyl)-1,3-propylenediamine, N,N′-bis-(3-aminopropyl)-1,3-propylenediamine, N,N,N′-tri-(2-aminoethyl)-ethylene diamine,
It is preferred that the one or more polyamines that are used in the method include at least one triamine and/or at least one tetramine. In fact, it is more preferred that two or more polyamines be used and that they be selected from diamines, triamines and tetramines. It is even more preferred that both a triamine and a tetramine are included. Preferred triamines include trimethylolpropane tris[poly(propylene glycol)amine terminated]ether (available as Jeffamine T-403), and diethylene triamine, and preferred tetramines include triethylenetetramine (TETA).
When a blend of a triamine and a tetramine is added to the reaction, it is preferred that the ratio of the number of functional groups supplied by the triamine relative to the number of functional groups supplied by the tetramine that is used is between about 100:0 to 0:100. As used herein, this ratio may be referred to as the ratio between the of equivalents of triamine:tetramine. A ratio of equivalents of triamine:tetramine of between about 90:10 and 10:90 is more preferred, yet more preferred is a ratio of between about 80:20 and 20:80, even more preferred is a ratio of between about 60:40 and 40:60, and yet more preferred is a ratio of about 50:50.
It has been found that the release rate of an agricultural active in the core of a microparticle having a polyurea shell, can be modulated by varying the ratio of the equivalents of a triamine such as Jeffamine T-403 and the equivalents of a tetramine such as triethylene tetramine. Accordingly, the parameter of the equivalents ratio of triamine to tetramine that is used in the interfacial polymerization reaction is one of the parameters that can be used to obtain a pre-selected controlled release rate of the active.
When the total amount of polyisocyanates and the total amount of polyamines that are contacted in the present method are considered, it is preferred that the ratio of the total equivalents of polyisocyanates to the total equivalents of polyamines is between about 4:1 and 1:4, more preferred is a ratio of 2:1 to 1:2, and yet more preferred is a ratio of about 1:1.
It is believed that the temperature at which the polymerization reaction takes place is a factor in obtaining a fully-formed and intact shell, without pores or other significant irregularities. Accordingly, it is preferred that the polymerization reaction is carried out at a temperature of between about 25° C. and about 90° C., and more preferred that the temperature be between about 40° C. and 75° C.
When the novel microcapsules are formed, the thickness of the shell wall can be controlled by varying the amount of the combined polyisocyanates and polyamines that are used, relative to the total amount of the liquid organic phase. The higher the level of polyisocyanates and polyamines with respect to the amount of the liquid organic phase, the thicker the polyurea shell wall that will be formed. In this specification the shell wall thickness is expressed in terms of the weight ratio of polyurea to core material. The weight ratio of the polyurea shell to the core can be controlled as described above, and desirably falls between about 5:100 and about 50:100. It is more preferred that the shell:core weight ratio is between about 10:100 and about 40:100, yet more preferred about 15:100 to about 30:100. However, since the thickness of the shell wall has an effect on the rate of release of an agricultural active from the core of the microcapsule when it is exposed to natural environmental conditions, shell wall thickness is a variable that can be controlled to provide a pre-selected release rate profile.
The terms “natural environmental conditions”, as used herein, are to be understood to mean the weather conditions that a microcapsule of the present invention will be exposed to when it is applied to a plant, a seed, or to soil, in a conventional soil-based growing environment. Such conditions include normal ambient rainfall, soil moisture, sunshine, temperature, biological activity, and the like.
When it is said that the agricultural active is released from the microcapsule at a “pre-selected controlled rate”, the terms “pre-selected controlled rate” refer to a pre-selected release profile of the active from the microcapsules, as can be represented by a plot of the cumulative amount of the active that has been released as a function of the time of exposure. One method of obtaining a microcapsule having a pre-selected controlled release rate is to determine the release rate of the active from the microcapsule under standardized test conditions (such as are described in detail in the Examples below) and then correlating the release profile obtained under standard conditions with the release profile of the active under normal environmental conditions. One of skill in the art of controlled released pesticides would understand that after this correlation is made several times, the release profile determined according to the standardized test methods can be used to predict the release rate under normal environmental conditions.
The controlled release forms of the present invention can be of any geometrical shape, but spherical microcapsules are preferred. A particularly useful form of the novel microcapsule includes a polyurea shell enclosing a core which comprises silthiopham, where the microcapsule has an average size of from about 2μ to about 8μ where the weight ratio of the shell to the core is from about 15:100 to about 30:100, and where the amount of silthiopham in the core is from about 30% to about 60%, by weight.
The microcapsules can be used in any manner in which other controlled release forms of agricultural actives are used, and can be applied to the soil, to seeds, roots, tubers, and any other form of plant propagation material, as well as to any part of a growing plant. The subject microcapsules can be used, without limitation, on such plants as corn, cereals, including wheat, barley, rye, and rice, vegetables, clovers, legumes, including beans, peas and alfalfa, vegetables, sugar cane, sugar beets, tobacco, cotton, rapeseed, sunflower, safflower, and sorghum, and on plant propagation material of such plants.
It is preferred that the microcapsules be used with legumes (members of the class Magnoliopsida and the order Fabales). It is more preferred that the plant be in the family Fabaceae (formerly Leguminosae) and the sub-family Papilionoideae or Faboideae, and even more preferred that the plant be selected from the group consisting of Pisum spp. (including the garden pea, P. sativum), Medicago spp. (including alfalfa, M. sativa), Arachis spp. (including peanuts, A. hypogaea), soybeans (including Glycine max, Glycine hispida), Vicia spp. (including vetches), Vigna spp. (including cowpeans), Vicia spp. (including fava bean, V. faba), trefoil, clovers and Phaseolus spp. (including P. vulgaris, P. lunatus, P. limensis, and P. coccineus). It is most preferred that the present microcapsules be used with wheat and soybeans.
The microcapsules can be applied to any type of plant seed as a coating, either neat or with sticking agents or other adjuvants.
When silthiopham is used as the first agricultural active, a preferred application is to apply the controlled release microcapsules to the seeds or the soil during the planting of winter wheat in order to obtain protective activity against Gaeumannomyces graminis in the fall and throughout the winter, but to retain sufficient activity to provide protection against renewed biological challenge in the spring.
In those embodiments of the invention where the high melting material is other than an agricultural active, the same general techniques, times, temperatures and concentrations can be used for the preparation of microcapsules that have been described herein for agricultural actives.
The following examples describe preferred embodiments of the invention. Other embodiments within the scope of the claims herein will be apparent to one skilled in the art from consideration of the specification or practice of the invention as disclosed herein. It is intended that the specification, together with the examples, be considered to be exemplary only, with the scope and spirit of the invention being indicated by the claims which follow the examples. In the examples all percentages are given on a weight basis unless otherwise indicated.
This example illustrates the production of microcapsules containing silthiopham as the agricultural active and with the use of a citric acid derivative as an organic solvent.
An aqueous solution of Lomar D surfactant (5.16 g; available from Henkel Corp., Morristown, N.J.) was prepared in 90.4 g water in a 250 ml beaker. The pH of the solution was adjusted to 7.2 by adding a small amount of citric acid, and the solution was heated to 55° C. An organic liquid solution was prepared by intermixing silthiopham (N-allyl-4,5-dimethyl-2-trimethylsilylthiophene-3-carboxamide, 16.00 g, available from Monsanto Company, St. Louis, Mo.), acetyltri-n-butyl-citrate (34.0 g; available as Citroflex A-4 from Morflex, Inc., Greensboro, N.C.), Desmodur N 3,200 (7.23 g; an aliphatic polyisocyanate (tri-isocyanate) based on hexamethylene diisocyanate, available from Bayer Corporation, Pittsburgh, Pa.) and meta-tetramethylenexylylene diisocyanate (TMXDI) (2.37 g; available from Miles Laboratories, Inc.) and then heating the mixture until all of the solids were dissolved. While the temperature of the solution was maintained at 50-55° C., the solution was agitated with a Silverson S4RT-4 mixer equipped with a six hole screen for 5-10 seconds at 4,200 rpm and the organic solution was added into the agitated solution in 20 seconds. The mixture was further agitated at 9,500 to 10,200 rpm for 40 seconds. After the formed emulsion was transferred into a 400 ml beaker equipped with a mechanic stirrer set at 625 rpm, an amine solution containing water (5.38 g), triethylenetetramine (m.w. 146.2), (1.10 g) and trimethylolpropane tris[poly(propylene glycol)amine terminated]ether (4.32 g, available as Jeffamine T-403, from Texaco Co. or Aldrich; m.w. ˜440) was added into the emulsion immediately. The temperature of the beaker was maintained at 55°-62° C. for 3 hours after which most of the isocyanate infrared absorbance peak at 2270 cm−1 had disappeared—indicating reaction of the isocyanate. A light yellow slurry (118 g) was collected. The average particle size was 4.2 microns. The weight ratio between wall and core was 30:100 and the amount of silthiopham in the core was 32% by weight.
This example illustrates the production of microcapsules containing silthiopham having thinner shells than in Example 1.
An aqueous solution of Lomar D (5.16 g) was added to 90.4 g water in a 250 ml beaker, and the pH of the solution was adjusted to 7.2 by adding a small amount of citric acid and the solution was heated to 55° C. An organic solution was prepared by intermixing silthiopham (16.00 g), Citroflex A-4 (34.0 g), Desmodur N 3,200 (4.82 g) and TMXDI (1.58 g) and then heating the mixture until all of the solids dissolved and the temperature of the solution was maintained at 50°-55° C. The aqueous solution was agitated with a Silverson S4RT-4 mixer equipped with a six hole screen for 5-10 seconds at 4,200 rpm and the organic solution was added to the agitated solution in 20 seconds. The mixture was further agitated at 9,500 to 10,200 rpm for 40 seconds. After the formed emulsion was transferred into a 400 ml beaker equipped with a mechanic stirrer set at 625 rpm, an amine solution containing water (5.38 g), triethylenetetramine (0.73 g) and Jeffamine T403 (2.88 g) was added into the emulsion immediately. The temperature of the beaker was remained at 55°-62° C. for 2 hours. The isocyanate infrared absorbance peak at 2270 cm−1 disappeared. 114 g of light yellow slurry was collected. The average particle size was 4.21 micron. The weight ratio between wall and core of the particles was 20:100 and the amount of active in the core was 32% by weight.
This illustrates the formation of microcapsules containing a higher level of silthiopham in the core.
An aqueous solution of Lomar D (5.16 g) was prepared by adding the surfactant to 90.4 g water in a 250 ml beaker. The pH of the solution was adjusted to 7.2 by adding a small amount of citric acid and heated to 55° C. An organic solution was prepared by mixing silthiopham (16.00 g), Citroflex A-4 (34.0 g), Desmodur N 3,200 (7.23 g) and TMXDI (2.37 g) together and then heating the mixture until all of the solids were dissolved and the temperature of the solution was maintained at 50°-55° C. The aqueous solution was agitated with a Silverson S4RT-4 mixer equipped with a six hole screen for 5-10 seconds at 4,200 rpm and the organic solution was added into the agitated solution in 20 seconds. The mixture was further agitated at 9,500 to 10,200 rpm for 40 seconds. After the formed emulsion was transferred into a 400 ml beaker equipped with a mechanic stirrer set at 625 rpm, an amine solution containing water (5.38 g), triethylenetetramine (1.10 g) and Jeffamine T-403 (4.32 g) was added into the emulsion immediately. The temperature of the beaker was remained at 55°-62° C. for 3 hours. Most of the isocyanate infrared absorbance peak at 2270 cm−1 disappeared. 118 g of light yellow slurry was collected. The average particle size was 4.2 micron. The weight ratio between wall and core was 30:100 and the amount of active in the core was 40% by weight.
This illustrates the preparation of microcapsules containing silthiopham having 20:100 wall:core weight ratio and 40% by weight active in the core.
An aqueous solution of Lomar D (5.16 g) was prepared by adding the surfactant to 90.4 g water in a 250 ml beaker. The pH of the solution was adjusted to 7.2 by adding a small amount of citric acid and the solution was heated to 55° C. An organic solution was prepared by mixing silthiopham (20.00 g), Citroflex A-4 (30.0 g), Desmodur N 3,200 (4.64 g) and TMXDI (1.74 g) together and then heating the mixture until all of the solids were dissolved and the temperature of the solution was maintained at 50°-55° C. The aqueous solution was agitated with a Silverson S4RT-4 mixer equipped with a six hole screen for 5-10 seconds at 4,200 rpm and the organic solution was added into the agitated solution in 20 seconds. The mixture was further agitated at 9,500 to 10,200 rpm for 40 seconds. After the formed emulsion was transferred into a 400 ml beaker equipped with a mechanic stirrer set at 625 rpm, an amine solution containing water (4.00 g), triethylenetetramine (0.74 g) and Jeffamine T-403 (2.90 g) was added into the emulsion immediately. The temperature of the beaker was maintained at 55°-62° C. for 2.5 hours. The isocyanate infrared absorbance peak at 2270 cm−1 disappeared. 118 g of light yellow slurry was collected. The average particle size was 4.5 micron. The weight ratio between the wall and core was 20:100 and the amount of active in the core was 40%.
This illustrates the production of microcapsules containing silthiopham where the capsules have a 15:100 weight ratio of wall:core.
Microcapsules were produced by the method described in Example 4, except that the organic solution contained 3.61 g of Desmodur N 3,200 and 1.19 g of TMXDI, and the amine solution contained 3.0 g of water, 0.55 g of triethylenetetramine and 2.16 g of Jeffamine T-403. 107 g of a light yellow product was collected and the average particle size was 3.4 microns. The weight ratio between the wall and the core was 15:100 and the amount of silthiopham in the core was 40% by weight.
This illustrates the effect of the wall thickness of microcapsules on the release rate of silthiopham into water.
Microcapsules containing silthiopham were produced by the method described in Examples 3-5, except that the ratio of equivalents of Desmodur N3,200 and TMXDI was maintained at 2:1, and the ratio of total isocyanate functional groups to total amine functional groups was maintained at 1:1 so that the polymerization reaction was stoichiometrically balanced. Microcapsules having wall:core weight ratios of 15:100, 20:100 and 30:100 were then prepared, and the properties of these microcapsules are shown in Table 1. The release rate of silthiopham was measured as described below.
aRatio of TETA:T-403 is equivalents of TETA:equivalents of T-403.
The release rate of an agricultural active from a controlled release formulation was measured by placing the controlled release formulation in a water sink so that at 100% release the total active present is less than approximately one third the water solubility level. The release solution is then agitated by shaking or stirring. At intervals, an aliquot is removed. The aliquot is filtered to separate the controlled release matrix from active dissolved in water. The filtered aliquot is then assayed for active present. Release curves are plotted to show hours after start of experiment vs percent of total active released.
When the release rate of microcapsules having a polyurea shell, or wall, enclosing a core containing silthiopham was tested, the following procedure was followed:
Release Solution Preparation:
Release rates of the microcapsule products of Samples 1-3 were measured as described above and the results are shown in FIG. 1. As can be seen, less than 10% of the silthiopham was released from sample 3 (having 30:100 wall:core ratio) after 1,500 hours, and the release rate increased as the wall:core ratio (essentially a measure of the thickness of the polyurea shell) decreased. This showed that the release rate could be modulated by controlling the wall:core ratio and that almost all of the active was present in the cores of the microcapsules. It was observed, however, that the release rate of each of the three samples was relatively low.
Microcapsules were prepared by the same methods as described in Examples 3-5, except that the amount of silthiopham that was loaded into the core was varied to provide silthiopham loadings of 50% and 60%, by weight, of the core. The wall:core ratio for the microcapsules was varied from 15:100, 20:100 and 30:100, as described above in Example 6. The release rates of each of the microcapsules having different silthiopham loading rates were measured and the results are shown in
This illustrates the effect of the amount of active in the core of the microcapsules on the release rate of silthiopham into water.
Microcapsules containing silthiopham were produced by the method described in Example 6, except that the wall:core ratio was maintained at 30:100, while the loading of silthiopham in the core was varied from 32% to 60%, by weight. Also, the reaction mixture was intermixed by the use of a Waring blender, rather than with a Silverson mixer. When the Waring blender was used, it was found that, in general, smaller microcapsules could be formed than when the Silverson mixer was used.
A 500 ml Waring blender was connected to a 0-140 volt Variac voltage controller to provide speed control. The aqueous solution was placed in the blender and mixed at a Variac setting of 30/140 V during the addition of the organic solution—over a period of about 20 seconds. After the organic solution had been added, the Variac was increased to 140/140 V to provide maximum speed for 40 seconds. The speed was then reduced to a 20/140 V Variac setting for the addition of the amine mixture. This took approximately one minute, after which the mixture was immediately transferred to a beaker being stirred at about 250-450 rpm by an overhead stirrer for the duration of the reaction.
The properties of the microcapsules are shown in Table 2.
aRatio of TETA:T-403 is equivalents of TETA to equivalents of T-403.
The release rate of silthiopham from the microcapsules was measured as described in Example 6, and the results are shown in FIG. 4. It is seen there that the sample having the highest level of silthiopham in the core provided the fastest release rate, with release rate decreasing as the level of silthiopham in the core decreased. All microcapsules were still releasing after 1,200 hours (50 days). This showed that the release rate could be modulated by controlling the amount of active initially placed in the core of the microcapsules.
Microcapsules having 15:100 and 20:100 shell:core ratios were also produced by the same methods and each had silthiopham loadings of 32%, 50% and 60% by weight in the core. Release rates for these samples were also measured as described in Example 6, and the results are shown in
This example illustrates the effect of particle size on the release rate of silthiopham from microcapsules having polyurea shells.
Microcapsules were prepared by the methods described in Example 6, except that the wall:core ratio was maintained at 30:100 and the loading of silthiopham in the core was maintained at 32% by weight. The average particle size was varied from 2.4μ (Sample 7—processed in a Waring blender as in Example 7) to 4.2μ (Sample 8—processed by a Silverson mixer as in Example 1). The release rate of silthiopham was measured as described in Example 6, and the results are shown in FIG. 7. As can be seen from that figure, as the microcapsule size increases, the release rate decreases. It was also seen that the initial release rate was higher for the smaller particles (5% REA for the 2.4μ particles versus less than 1% REA for the 4.2μ particles). This test was repeated for microcapsules that were formed by the same method, but had a shell:core ratio of 20:100, 32% loading of silthiopham in the core, and particle sizes of 2.1μ and 4.1%. Release rates of silthiopham were measured for these particles by the same methods and the release curves are shown in FIG. 8.
The data from both curves shows that the release rate of the active can be modulated by controlling the size of the microcapsule. It is believed that size can be controlled by, for example, control on the shear severity and duration during blending of the aqueous and organic phase liquid, and by controlling the temperature and the viscosity of the two phases. It is believed that microcapsules between about 2μ and about 8μ are preferred for the present applications, although both larger and smaller microcapsules are possible.
This example illustrates the effect of the composition of the shell wall on the release rate of silthiopham from microcapsules having polyurea shells.
In this set of experiments, microcapsules were produced by the methods described in Example 6, except that the wall:core weight ratio was maintained at 20:100 and the loading of silthiopham in the core was maintained at 50% while the amount of Jeffamine T-403 used in the reaction was increased from 0 to 100%, and a Waring blender was used for mixing as described in Example 7. Properties of the resulting microcapsules are summarized in Table 3. The average particle size for all of the samples ranged from 2.2 to 2.4 microns, which indicated that the ratio of TETA and Jeffamine T-403 did not significantly effect the average particle size. In fact, the average particle size of the microcapsule was found to depend on (1) the agitation during blending of the aqueous and organic liquids, (2) the viscosity of the dispersed or emulsified organic phase which contains the active, the solvent, and the isocyanates and (3) the emulsifier or the dispersion reagent. The initial release is associated with the composition of the shell. As can be seen from the data in Table 3, the initial release remained at 0.6% level when the ratio between the equivalents of TETA and the equivalents of Jeffamine T-403 was below 50%/50%. However the initial release of silthiopham was increased from 1.4% to even 17% when the ratio between TETA and Jeffamine T-403 was decreased from 50%/50% to 0/100%. This result agrees with the release profiles of silthiopham in water, which are shown in
This experiment was repeated with microcapsules having shell:core ratios of 30:100, rather than 20:100, and the effect of varying the TETA/T-403 ratio on the release rate was found to be the same as for the thinner capsule wall. The release rate results for the microcapsules having a 30:100 shell:core ratio are shown in
In general an amine group in the polyamine molecule will react with an isocyanate to give polyurea. In this process the reaction occurs at the interface of the organic droplet and the aqueous solution, and a shell composed of polyurea forms. It is believed that the density or the permeability of the shell will depend on the composition of the polyurea. Since TETA with four amine groups is a much smaller molecule than Jeffamine T-403 with three amine groups, it is believed that the polyurea shell made with higher TETA concentration will have the more condensed shell therefore provide slower release rate of silthiopham. Therefore, the results show that the release profiles of silthiopham in water can be controlled by varying the ratios of TETA and Jeffamine T-403 used during the polymerization.
aThe ratio of TETA/T-403 is given as equivalents of TETA per equivalent of T-403.
This illustrates the stability of microencapsulated silthiopham.
The stability of the encapsulated silthiopham products was studied by measuring the initial release of silthiopham in the products after they had aged for a certain period after synthesis. As can be seen in Table 4, the stability of the microcapsules varies somewhat between microcapsules having different synthesis parameters, but is, in general, acceptable for a commercially useful product. The initial release of Sample 8 was slightly increased to 1.8% from 0.95% after 81 days. However the initial release of Sample 1 was increased to 11% from 1.5% after 52 days.
This illustrates a study of the microcapsules of the present invention by scanning electron microscope.
A sample of microcapsules containing silthiopham in the core was produced by the methods described in Example 6, except that the capsules had a 50% loading of silthiopham in the core with a shell wall:core ratio of 30:100, and mixing was carried out in a Waring blender as described in Example 7. The average particle size as measured by a Coulter counter was 2.4 microns, which is very close to what is observed by a scanning electron micrograph, which is shown in FIG. 11. The microcapsules have a spherical shape with some small dimples on the surface. Since the cores of these microcapsules contain 50% of silthiopham, the encapsulated active imposed some stress on the shell and thus the small dimple is believed to be associated with the stress appeared.
The sample shown in
This example illustrates the formation of a eutectic mixture with silthiopham and tebuconazole.
The melting temperature at one atmosphere was measured for pure silthiopham and for pure tebuconazole and for mixtures of 10:90, 20:80, 30:70, 40:60, 50:50, 60:40, 70:30, 80:20, and 90:10 silthiopham:tebuconazole, on a weight basis. The results are shown in
This example illustrates the formation of a eutectic mixture with silthiopham and simeconazole.
The melting temperature at one atmosphere was measured for pure silthiopham and for pure simeconazole and for mixtures of the two materials as described in Example 12. The results are shown in
This example illustrates the formation of a eutectic mixture with silthiopham and 1-(4-fluorophenyl)-2-(1H-1,2,4-triazole-1-yl)-ethanone.
The melting temperature at one atmosphere was measured for pure silthiopham and for pure 1-(4-fluorophenyl)-2-(1H-1,2,4-triazole-1-yl)-ethanone and for mixtures of 10:90, 20:80, 30:70, 40:60, 50:50, 60:40, 70:30, 80:20, and 90:10 silthiopham: 1-(4-fluorophenyl)-2-(1H-1,2,4-triazole-1-yl)-ethanone, on a weight basis. The results are shown in
This example illustrates the production of microcapsules containing silthiopham and tebuconazole in the core and where the method is free of the use of a solvent.
An aqueous solution was prepared by adding Lomar D (5.16 g) to 90.4 g water in a 250 ml beaker, and the pH of the solution was adjusted to 7.2 by adding a small amount of citric acid. The solution was heated to 65° C. An organic liquid solution was prepared by intermixing silthiopham (25.00 g), tebuconazole (25.00 g), Desmodur N 3,200 (4.82 g) and TMXDI (1.58 g) and then heating the mixture until the solids were dissolved and the temperature of the solution was maintained at 65°-70° C. The aqueous solution was agitated with a Silverson S4RT-4 mixer equipped with a six hole screen for 5-10 seconds at 4,200 rpm and the organic solution was added into the agitated solution in 20 seconds. The mixture was further agitated at 9,500 to 10,200 rpm for 40 seconds. After the formed emulsion was transferred into a 400 ml beaker equipped with a mechanic stirrer set at 625 rpm, an amine solution containing water (4.00 g), triethylenetetramine (0.73 g) and Jeffamine T-403 (2.88 g) was added into the emulsion immediately. After maintaining the temperature of the mixture at 65°-70° C. for 0.5 hour, the isocyanate infrared absorbance peak at 2270 cm−1 disappeared. 108.3 g of yellow slurry was collected after 1 hour. The weight ratio between the wall and the core was 20:100.
This illustrates the production of microcapsules containing silthiopham and tebuconazole in the absence of a solvent, but with a higher wall:core ratio that in Example 15.
Microcapsules were produced by the method described in Example 15, except that the organic solution contained 7.23 g of Desmodur N 3,200 and 2.37 g of TMXDI, and the amine solution contained 6.0 g of water, 1.1 g of triethylenetetramine and 4.32 g of Jeffamine T-403. The isocyanate peak at 2270 cm−1 disappeared after 1.5 hours, and 107 g of a light yellow product was collected after 2 hours. The weight ratio between the wall and the core was 30:100.
This illustrates the production of microcapsules containing silthiopham and tebuconazole in the absence of a solvent, but with a higher wall:core ratio that in Example 15 and with only one type of amine.
Microcapsules were produced by the method described in Example 15, except that the organic solution contained 9.22 g of Desmodur N 3,200 and 3.03 g of TMXDI, and the amine solution contained 6.0 g of water, 2.8 g of triethylenetetramine (TETA) and no Jeffamine T-403. The isocyanate peak at 2270 cm−1 disappeared after 2 hours, and 133 g of a light yellow product was collected after 2.25 hours. The weight ratio between the wall and the core was 30:100.
The product appears as a light yellow slurry and no crystals can be observed in the product under optical microscopy. The images from scanning electron microscopy (SEM) suggest that spherical microcapsules were formed.
This example illustrates the use of microcapsules formed according to the present invention to form a coating on wheat seed.
Wheat seed (100 g, of the species triticum aestivum, var. “Consort”) was placed into the bowl of a Hege 11 seed coating machine. A sample (0.2 ml) of a formulation prepared according to the procedure of Example 1, but having a polyurea shell wall thickness of 30%, a concentration of silthiopham in the core of 60%, by weight, and an amine ratio between TETA and Jeffamine T403 of 50:50. This sample was diluted with water (0.8 ml) to afford a formulation with a silthiopham concentration of 125 g/1000 ml. This formulation was applied via syringe into the turning Hege bowl filled with wheat (100 g). The Hege bowl was turned on for 30 sec to provide uniform distribution and coating of seeds.
This example illustrates the use of microcapsules formed according to the present invention to form a coating on wheat seed.
The same procedure as described in Example 18 was used to coat wheat seed, except that 0.012 ml of Vinamul 18132 was added to the formulation containing the silthiopham. Wheat seed coated with the microcapsules of the present invention were obtained.
All references cited in this specification, including without limitation all papers, publications, patents, patent applications, presentations, texts, reports, manuscripts, brochures, books, internet postings, journal articles, periodicals, and the like, are hereby incorporated by reference. The discussion of the references herein is intended merely to summarize the assertions made by their authors and no admission is made that any reference constitutes prior art. Applicants reserve the right to challenge the accuracy and pertinency of the cited references.
In view of the above, it will be seen that the several advantages of the invention are achieved and other advantageous results obtained.
As various changes could be made in the above methods and compositions without departing from the scope of the invention, it is intended that all matter contained in the above description and shown in the accompanying drawings shall be interpreted as illustrative and not in a limiting sense.
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