Plant protecting and regulating compositions – Plant growth regulating compositions – Organic active compound containing
Reexamination Certificate
2001-09-21
2002-07-30
Clardy, S. Mark (Department: 1616)
Plant protecting and regulating compositions
Plant growth regulating compositions
Organic active compound containing
C504S359000
Reexamination Certificate
active
06426319
ABSTRACT:
The present invention relates to new delivery systems for cyclopropenes in which compositions comprising the cyclopropene and a molecular encapsulation agent complex comprise additional components which provide enhanced release of the cyclopropene from the molecular encapsulating agent using water. Such cyclopropenes and their derivatives, such as methylcyclopropene, are capable of inhibiting the ethylene response in plants. The cyclopropene/molecular encapsulating agent complexes provide a convenient means for storing and transporting the cyclopropenes which are reactive gases and highly unstable because of oxidation and other potential reactions. Such complexes also provide convenient methods of delivering these compounds to plants in order to extend the plant's shelf life.
It is well known that ethylene can cause the premature death of plants or plant parts including, for example, flowers, leaves, fruits, and vegetables through binding with certain receptors in the plant. Ethylene also promotes leaf yellowing and stunted growth as well as premature fruit, flower, and leaf drop. Because of these ethylene-induced problems, very active and intense research presently concerns the investigation of ways to prevent or reduce the deleterious effects of ethylene on plants. U.S. Pat. No. 5,518,988 discloses the use of cyclopropene and its derivatives, including methylcyclopropene, as effective blocking agents for ethylene binding. However, a major problem with these compounds is that they are typically unstable gases which present explosive hazards when compressed. As a solution to these problems, U.S. Pat. No. 6,017,849 discloses a method of incorporating these gaseous compounds into a molecular encapsulation agent complex in order to stabilize their reactivity and thereby provide a convenient and safe means of storing, transporting and applying or delivering the active compounds to plants. For the most active cyclopropene derivative disclosed in U.S. Pat. No. 5,518,988, 1-methylcyclopropene, the preferred molecular encapsulation agent is a cyclodextrin, with &agr;-cyclodextrin being the most preferred . The application or delivery of these active compounds to plants is accomplished by simply adding water to the molecular encapsulation agent complex. The complex is prepared according to the methods disclosed in U.S. Pat. No. 6,017,849 which provides the material in the form of a powder.
The 1-methylcyclopropene/&agr;-cyclodextrin complex noted above releases the 1-methylcyclopropene very quickly. However, in order to accomplish this release large amounts of water are required, at least ten times and preferably twenty times the weight of the 1-methylcyclopropene/&agr;-cyclodextrin complex. It would be advantageous to accomplish complete release of the cyclopropene from the complex using a minimal amount of water. This would allow a user to treat flowers, fruits, or vegetables with the cyclopropene gas directly in shipping containers, rather than a large treatment container, chamber, or room.
We have surprisingly found that small amounts of absorbed water are sufficient to release 1-methylcyclopropene from the 1-methylcyclopropene/&agr;-cyclodextrin complex. In one embodiment of the present invention powdered complex is mixed with a water absorbent material such as a powdered superabsorbent polymer. Such polymers include, for example, sodium polyacrylate. The mixture is then placed in a sachet which can be made from a variety of materials including, as one example, filter paper. When this sachet is dipped in water for 10 seconds and then placed in a container, it slowly releases the 1-methylcyclopropene gas. In another embodiment of the invention, a deliquescent compound is mixed with the powdered complex and placed in a sachet. When this sachet is placed in a humid environment, such as an environment typical for the storage of flowers, fruits, and vegetables, the 1-methylcyclopropene gas again is slowly released. Although the delivery systems of this invention provide slow release of 1-methylcyclopropene they still provide complete release. This same process is equally applicable to other cyclopropene/molecular encapsulation agent complexes.
The present invention is, therefore, a composition comprising:
a) a molecular encapsulation agent within which a cyclopropene of the formula:
wherein R
is hydrogen or a substituted or unsubstituted alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, phenyl, or naphthyl group; wherein the substituents are independently halogen, alkoxy, or substituted or unsubstituted phenoxy;
is encapsulated;
b) optionally one or more adjuvants; and
c) a water absorbent material.
As used herein, the term “alkyl” means both straight and branched chain (C
1
-C
20
) radicals which include, for example, methyl, ethyl, n-propyl, isopropyl, 1-ethylpropyl, n-butyl, tert-butyl, isobutyl, 2,2-dimethylpropyl, pentyl, octyl, and decyl. The terms “alkenyl” and “alkynyl” mean (C
3
-C
20
)alkenyl and (C
3
-C
20
)alkynyl groups such as, for example, 2-propenyl, 2-butenyl, 3-butenyl, 2-methyl-2-propenyl, and 2-propynyl. The term “cycloalkylalkyl” means a (C
1
-C
15
) alkyl group substituted with a (C
3
-C
6
) cycloalkyl group such as, for example cyclopropylmethyl, cyclopropylethyl, cyclobutylmethyl, and cyclopentylethyl. The term “haloalkyl” means an alkyl radical wherein one or more of the hydrogen atoms have been replaced by a halogen atom. The term “halogen” means fluorine, chlorine, bromine, and iodine.
Preferably, R is (C
1
-C
10
) alkyl. More preferably, R is (C
1
-C
8
) alkyl. Even more preferably R is (C
1
-C
4
) alkyl. Most preferably, R is methyl.
Preferred encapsulating agents include cyclodextrins, crown ethers, polyoxyalkylenes, polysiloxanes, and zeolites. More preferred encapsulating agents include &agr;-cyclodextrin, &bgr;-cyclodextrin, and &ggr;-cyclodextrin. The most preferred encapsulating agent, particularly when the cyclopropene is 1-methylcyclopropene, is alpha-cyclodextrin. The most preferred encapsulating agent will vary depending upon the size of the R substituent. However, as one skilled in the art will appreciate, any cyclodextrin or mixture of cyclodextrins, cyclodextrin polymers as well as modified cyclodextrins can also be utilized pursuant to the present invention. Cyclodextrins are available from Wacker Biochem Inc., Adrian, Mich. or Cerestar USA, Hammond, Ind., as well as other vendors.
As used herein, all percentages are percent by weight and all parts are parts by weight, unless otherwise specified, and are inclusive and combinable. All ratios are by weight and all ratio ranges are inclusive and combinable. All molar ranges are inclusive and combinable.
The cyclopropenes applicable to this invention are known materials prepared using the processes disclosed in U.S. Pat. Nos. 5,518,988 and 6,017,849. The cyclopropene/molecular encapsulation agent complexes of the present invention are prepared by contacting the cyclopropene with a solution or slurry of the molecular encapsulation agent and then isolating the complex, again using general processes disclosed in U.S. Pat. No. 6,017,849. In the case of 1-methylcyclopropene, the gas is bubbled through a solution of &agr;-cyclodextrin in water from which the complex first precipitates and is then isolated by filtration.
It is often desirable to include in the composition one or more adjuvants, such as extenders, binders, lubricants, surfactants and/or dispersants, wetting agents, spreading agents, dispersing agents, stickers, adhesives, defoamers, thickeners, emulsifying agents and the like. Such adjuvants commonly used in the art can be found in the John W. McCutcheon, Inc. publication
Detergents and Emulsifiers, Annual,
Allured Publishing Company, Ridgewood, N.J., U.S.A.
A wide variety of water absorbent materials may be used in the compositions of this invention. These include one or more organic materials such as superabsorbent polymers, such as, for example, sodium polyacrylate (crosslinked), polysaccharides, acrylamide/acrylate copolymers, and carboxymethylcellulose; one or more
Clardy S. Mark
Rogerson Thomas D.
Rohm and Haas Company
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