Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Ester doai
Reexamination Certificate
2001-09-14
2003-04-01
Levy, Neil S. (Department: 1616)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Ester doai
C424S405000, C504S101000, C504S212000, C504S272000, C514S521000
Reexamination Certificate
active
06541516
ABSTRACT:
BACKGROUND OF THE INVENTION
Agriculturally active chemicals are most preferably applied in the form of aqueous emulsions, solutions or suspensions. Occasionally, they may also be applied in the form of a dust wherein the active ingredient is adsorbed onto or mixed with a finely divided inert carrier material, such as, china clay, or the like. With such powdered or dust compositions, drift due to wind is a problem and consequently, liquid formulations are preferred.
One of the problems with such liquid formulations is the fact that chemicals possessing agricultural activity, particularly those high load active concentrations, often exhibit extreme insolubility in water. This results in their having to be dissolved either in organic solvents or utilized in the form of emulsions subsequent to phase separation or suspensions. With respect to the use of organic solvents, such as xylene, or phenolic esters, these are generally disadvantageous from an environmental and cost viewpoint. Particularly, such organic chemicals may exhibit toxicity or side-effects which may be adverse to the effect of the agricultural chemical itself or to the subsequent fruit or vegetable produced in the particular agricultural use. This toxicity may also be disadvantageous with respect to inhalation during handling and flammability.
When attempts are made to provide emulsified or suspension formulations, difficulties are encountered with respect to providing a desirably high concentration of the agriculturally active ingredient. Thus, when such agriculturally active chemicals are formulated into a macroemulsion (sometimes referred to herein as an emulsion), it is difficult to maintain the emulsified state. This, in turn, creates problems in maintaining a uniform formulation and subsequent plant dosage, particularly, when the formulation is diluted with water for application on the plants.
U.S. Pat. No. 5,317,042 disclosed a clear stable, efficacious aqueous microemulsion of an agriculturally active chemical, alone, or in a complex mixture, obtained by incorporating the chemical in an inert matrix composition containing a defined mixture of nonionic surfactant to form a microemulsion concentrate which is subsequently diluted with water for plant treatment. Patentee's inert matrix composition consists of a predetermined mixture of nonionic surfactants which include nonylphenol ethoxylate having an HLB of >6. However, the presence of nonylphenol ethoxylate in the formulation is considered detrimental from an ecological standpoint.
U.S. Pat. No. 6,187,715 described water-based microemulsions of a lower alkyl ester of quinoxalinyl herbicide including 20 to 50 wt. % of a heavy aromatic petroleum distillate.
Accordingly, it is an object of this invention to provide a substantially stable homogeneous, water soluble microemulsion containing at least 5 wt. % of an active pyrethroid insecticide or a triazole fungicide which is free of toxic and environmentally objectionable surfactants.
Another object is to provide a stable concentrate containing such actives in high load which is readily soluble in water and suitable for spraying crops.
These and other benefits and objectives will become apparent from the following description and disclosure.
SUMMARY OF THE INVENTION
In accordance with the present invention there is provided a stable, liquid homogeneous concentrate matrix comprising MICROFLEX® admixed with a hydrophobic oil, preferably a heavy aromatic petroleum oil distillate boiling between 100° F. and 250° F., combined in a weight ratio of between about 4.5-50:1 MICROFLEX® to oil, which corresponds to about 2-18 wt. % of oil therein.
Within these ranges, preferably 5-15%, and, most preferably 2-12%, the actives dissolve readily in the concentrate and stable, homogeneous compositions are obtained upon dilution with water for spraying. The present concentrate thus can be diluted with up to 99.9 wt. % water to provide a homogeneous liquid spray for treating plants.
The general formula for the MICROFLEX® composition is described in the SUMMARY OF THE INVENTION, elements (b) through (f) in U.S. Pat. No. 6,045,816. The teaching of this patent is incorporated herein by reference.
The above matrix concentrate is capable of loading up to 25 wt. % of an active pyrethroid insecticide or triazole fungicide. A pyrethroid is a class of well known and widely-used insecticides of which cypermethrin, D-allethrin, permethrin, piperonyl butoxide and tetramethrin are representative examples.
Other agricultural active chemicals which may be included in the compositions of the invention are: permethrin; permethrin+Kathon®, D-allethrin; tetramethrin; deltamethrin; piperonyl butoxide; mixed pyrethroids; dicofol; tefluthrin; resmethrin; phenothrin; kadethrin; bifenthrin; cyhalothrin; cycloprothrin; tralomethrin; cyfluthrin; fenvalerate and isomers; fenpropathrin; fluvalenate; rotenone; biphenyl compounds like, methoxychlor; chlorbenzilate; bromopropylate and chlorfenethol.
DETAILED DESCRIPTION OF THE INVENTION
The basic concentrate of this invention comprises a mixture of MICROFLEX® and a hydrophobic oil such as heavy aromatic petroleum oil distillate. To achieve a clear, homogeneous composition upon dilution, the ratio of oil should be 4.5 to 50:1. More desirably a weight % of oil of 5-15% oil is employed to obtain a homogeneous sprayable solution.
The oil distillates suitably employed for the present MICROFLEX® mixture have an average boiling point of between 100° and 250° F. and are commercially available as fractions from crude oil distillation. Typical of such oils are Exxon 200, Aromatic 150, Aromatic 200 available from Exxon and Texaco 400. Generally these oil fractions contain a major portion of aromatic solvent naphtha and a minor portion of middle distillate solvent extract of which about a 55-65/35-45 mixture is most desirable. Normally these oils, which contain predominantly aromatics, are compounds having 8 to 15 carbon atoms and primarily 10-12 carbon atoms. The flash point of these distillates is preferably above 200° F.
As indicated above the MICROFLEX® composition of this invention is a mixture and contains
(i) 0 to about 60 wt. %, preferably 0.15 to 40 wt. %, of a N—C
1
to C
4
alkyl lactam such as an N-alkyl pyrrolidone, an N-alkyl caprolactam or mixtures thereof;
(ii) from about 0.002 to about 40 wt. %, preferably 0.05 to 29 wt. % of a N—C
8
to C
18
alkyl lactam such as an N-alkyl pyrrolidone, an N-alkyl caprolactam and mixtures thereof,
(iii) 0 to abut 30 wt. %, preferably 0.5 to 15 wt. %, of an ethylene oxide/propylene oxide block copolymer surfactant;
(iv) 0.03 to about 80 wt. %, preferably 40 to 70 wt. %, of an alkoxylated castor oil, tristyryl phenol ethoxylate or a mixture thereof and
(v) 0 to about 10 wt. %, preferably 0.005 to 6 wt. % of a phosphate ester buffer.
In the above MICROFLEX® composition, N-methyl- and N-octyl-lactams, particularly N-methyl- and N-octyl-pyrrolidones, are preferred. Although the above lactams can be ring substituted with C
1
to C
4
alkyl radicals, unsubstituted species are more desirable.
In general, the present concentrate containing the active component is prepared by initially combining MICROFLEX® as an anhydrous mixture with the oil fraction and then gradually adding between about 5 to about 25% by weight of the active component. This operation can be carried out under continuous agitation over a period of from about 0.5 to about 6 hours at ambient temperature up to a temperature below the boiling point of the oil. The resulting mixture is a substantially clear, somewhat viscous liquid which can be diluted with up to 99.9 wt. % of water to form a stable microemulsion suitable for treating a plant area. The concentrate when diluted with either soft or (100-1000 ppm) hard water is stable at both low and high temperatures over the two-week period tested. The concentration of the active component in the diluted concentrate can vary widely depending on the dosages conventionally recommended, the type of plant to be treated, the atmospheric conditions encountered in
Jon Domingo I.
Narayanan Kolazi S.
Davis William J.
ISP Investments Inc.
Katz Walter
Levy Neil S.
Maue Marilyn J.
LandOfFree
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