Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...
Reexamination Certificate
2002-12-20
2004-11-02
Levy, Neil S. (Department: 1616)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Having -c-, wherein x is chalcogen, bonded directly to...
C424S405000, C424S407000
Reexamination Certificate
active
06812242
ABSTRACT:
The present invention relates to novel compositions intended for controlling insects, and to a control method using the said compositions.
Insecticidal compounds of the phenylpyrazole type which may be used for controlling insects are known, in particular from patent applications EP 295,117, WO 87/3781, 93/6089 and 94/21606. EP 295,117 also mentions compositions in the form of edible baits comprising from 0.01% to 5% of such active materials.
It is often desirable to place such baits in areas in which undesirable insects are liable to circulate, in particular when these insects are ants, cockroaches, wasps and termites, and most particularly insects which travel in a group or in columns such as ants. The areas concerned may in particular include living quarters or areas outside these quarters such as patios or pleasure gardens or passageways.
When it is desired to apply the compositions in the form of liquid baits, it is convenient to distribute these baits in the form of drops, and it is desirable for these drops to remain where they are.
More particularly, when it is desired to apply these compositions in the form of drops, it is desirable for the said drops to remain where they are for the longest possible period, in order for the insects to be able to come effectively into contact with these compositions, and to ingest them as much as possible. In the sense of the present invention, the term drop means a volume of rounded shape of between 0.01 and 1 ml, preferably between 0.01 and 0.1 ml, whose height, for an isolated drop on a flat surface, is greater than 1 mm, preferably greater than 3 mm.
Such an application then poses a certain number of difficulties.
It is thus necessary for these drops to disappear as slowly as possible, in particular by spreading or by evaporation.
On account of the diverse nature of the supports on which these drops may be deposited, it is also necessary for them not to be absorbed too rapidly, for example in the case of porous supports.
In the case of multiple applications from a single storage container, it is also desirable for the insecticidal composition to retain its performance despite repeated opening and closing of the packaging.
One aim of the invention is to overcome these difficulties in total or in part.
Another aim of the invention is to propose advantageous compositions for application by deposition of drops.
Another aim of the invention is to provide compositions comprising at least one insecticidal active material of phenylpyrazole type which is applicable in drop form, in particular under conditions favouring the evaporation or absorption of liquids.
Another aim of the invention is to provide compositions which are attractant and nourishing for insects, especially for gregarious insects and/or insects which live in a society such as ants, these compositions comprising at least one insecticidal active material of phenylpyrazole type.
Another aim of the invention is to propose insecticidal compositions which retain their performance in the course of repeated use, in particular in the course of frequent opening of the packages containing them.
It has now been found that these aims could be achieved, in total or in part, using the control compositions and method according to the invention which are described in detail below. It is pointed out that the percentages indicated in the present text are weight/weight percentages, except where specifically indicated otherwise.
The subject of the present invention is thus, firstly, insecticidal compositions comprising:
a) between 0.001 and 5%, preferably between 0.05 and 0.5%, of a compound of formula (I):
in which:
R
1
is a halogen atom or a CN or methyl group;
R
2
is S(O)
n
R
3
;
R
3
is alkyl or haloalkyl;
R
4
represents a hydrogen or halogen atom; or a radical NR
5
R
6
, S(O)
m
R
7
, C(O)R
7
or C(O)O—R
7
, alkyl, haloalkyl or OR
8
or a radical —N═C(R
9
)(R
10
);
R
5
and R
6
independently represent a hydrogen atom or an alkyl, haloalkyl, C(O)alkyl or S(O)
r
CF
3
radical; or R
5
and R
6
may together form a divalent alkylene radical which may be interrupted by one or two divalent hetero atoms, such as oxygen or sulphur;
R
7
represents an alkyl or haloalkyl radical;
R
8
represents an alkyl or haloalkyl radical or a hydrogen atom;
R
9
represents an alkyl radical or a hydrogen atom;
R
10
represents a phenyl or heteroaryl group optionally substituted with one or more halogen atoms or groups such as OH, —O-alkyl, —S-alkyl, cyano or alkyl;
R
11
, and R
12
represent, independently of each other, a hydrogen or halogen atom;
R
13
represents a halogen atom or a haloalkyl, haloalkoxy, S(O)
q
CF
3
or SF
5
group;
m, n, q and r represent, independently of each other, an integer equal to 0, 1 or 2;
X represents a trivalent nitrogen atom or a radical C—R
12
, the other three valency positions of the carbon atom forming part of the aromatic ring;
with the proviso that when R
1
is methyl, then R
3
is haloalkyl, R
4
is NH
2
, R
11
is Cl, R
13
is CF
3
and X is N;
b) between 0.05 and 10%, preferably between 0.1 and 5%, of a thickener; and
c) between 5 and 50%, preferably between 10 and 40%, of propylene glycol, the compound of formula (I) being in the dissolved state in the said composition.
The alkyl radicals in the definition of formula I generally comprise from 1 to 6 carbon atoms. The ring formed by the divalent alkylene radical representing R
5
and R
6
as well as by the nitrogen atom to which R
5
and R
6
are attached is generally a 5-, 6- or 7-membered ring.
When the compositions according to the invention are applied in the form of drops deposited in a place where insects, preferably ants, are liable to pass, in particular a place consisting of an absorbent support, the compositions according to the invention are particularly advantageous on account of their slow spreading.
More precisely, the height of a drop of the said compositions above a flat surface on which it is deposited remains advantageously greater than 1 mm, preferably greater than 3 mm, after a period of more than 1 day, preferably of more than 2 days, at ambient temperature.
Furthermore, these compositions are of improved storage in the case where their commercial packaging is frequently opened and closed by the user.
The compositions according to the invention are relatively viscous but, despite this, the active material is uniformly distributed in the composition, by virtue of the nature of this composition.
The compound of formula (I) may be prepared according to one of the methods described in Patent Applications WO 87/3781, 93/6089, 94/21606 and EP 295,117 or alternatively by another method from within the general knowledge of those skilled in the art competent in chemical synthesis. This compound is also referred to in the present text by the term active material.
Among the thickeners which may in particular be used are a heteropolysaccharide, a polyacrylate salt, in particular the ammonium salt, a copolymer of vinylpyrrolidone and vinyl acetate, a polyglycol such as polyethylene glycol, starch or gum arabic.
According to a preferred variant of the composition according to the invention, the composition also comprises from 30 to 70%, preferably from 40 to 60%, of sugars. This composition variant is of considerably enhanced appetency for ants. The sugars are chosen in particular from mono-, oligo- or polyorganosaccharides, especially from sucrose, lactose, fructose, dextrose or glucose, or alternatively molasses or honey.
A preferred class of compounds of formula (I) comprises the compounds where R
1
is CN and/or R
3
is haloalkyl and/or R
4
is NH
2
and/or R
11
and R
12
are, independently of one another, a halogen atom and/or R
13
is haloalkyl.
According to a particularly advantageous variant of the invention, the compound of formula (I) used in the invention is 5-amino-3-cyano-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulphinyl]-1H-pyrazole, which is referred to in the examples by the term “fipronil”.
The compositions which form the subject of the inventi
Derois Jean
Gautier Martine
BASF Agro B.V. Arnhem (NL) -Wadenswil Branch
Burns Doane Swecker & Mathis L.L.P.
Levy Neil S.
LandOfFree
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