U.S. patent application number 14/035498 was filed with the patent office on 2014-03-27 for pesticidal active mixtures comprising isoxazoline compounds i.
This patent application is currently assigned to BASF SE. The applicant listed for this patent is Florian KAISER, Karsten KOERBER, Juergen LANGEWALD. Invention is credited to Florian KAISER, Karsten KOERBER, Juergen LANGEWALD.
Application Number | 20140087943 14/035498 |
Document ID | / |
Family ID | 41143519 |
Filed Date | 2014-03-27 |
United States Patent
Application |
20140087943 |
Kind Code |
A1 |
KOERBER; Karsten ; et
al. |
March 27, 2014 |
Pesticidal Active Mixtures Comprising Isoxazoline Compounds I
Abstract
The present invention relates to pesticidal mixtures comprising
as active compounds 1) at least one isoaxazoline compound I of the
formula (I) ##STR00001## wherein R.sup.1, R.sup.2, R.sup.3,
R.sup.4, R.sup.5 and A are defined in the description; and 2) at
least one active compound II selected from a group A comprising
acteylcholine esterase inhibitors, GABA-gated chloride channel
antagonists, sodium channel modulators, nicotinic acteylcholine
receptor agonists/antagonists, chloride channel activators,
juvenile hormone mimics, compounds affecting the oxidative
phosphorylation, inhibitors of the chitin biosynthesis, moulting
disruptors, inhibitors of the MET, voltage-dependent sodium channel
blockers, inhibitors of the lipid synthesis and other compounds as
defined in the description, in synergistically effective amounts.
The invention relates further to methods and use of these mixtures
for combating insects, arachnids or nematodes in and on plants, and
for protecting such plants being infested with pests, especially
also for protecting plant propagation material as like seeds.
Inventors: |
KOERBER; Karsten;
(Eppelheim, DE) ; KAISER; Florian; (Mannheim,
DE) ; LANGEWALD; Juergen; (Mannheim, DE) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
KOERBER; Karsten
KAISER; Florian
LANGEWALD; Juergen |
Eppelheim
Mannheim
Mannheim |
|
DE
DE
DE |
|
|
Assignee: |
BASF SE
Ludwigshafen
DE
|
Family ID: |
41143519 |
Appl. No.: |
14/035498 |
Filed: |
September 24, 2013 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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13003037 |
Jan 7, 2011 |
8563474 |
|
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PCT/EP2009/058517 |
Jul 6, 2009 |
|
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14035498 |
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61079318 |
Jul 9, 2008 |
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Current U.S.
Class: |
504/100 ;
514/229.2; 514/30; 514/340; 514/341; 514/378 |
Current CPC
Class: |
A01N 43/80 20130101;
A61K 31/7048 20130101; A61P 33/14 20180101; A01N 43/40 20130101;
A01N 43/80 20130101; A61K 31/5395 20130101; A01N 43/88 20130101;
A61K 31/42 20130101; A01N 43/50 20130101; A01N 53/00 20130101; A01N
43/90 20130101; A01N 43/40 20130101; A61P 33/00 20180101; A61K
31/4439 20130101; A61K 31/4427 20130101; A61K 31/455 20130101; A61K
31/277 20130101; A01N 43/90 20130101; A01N 43/80 20130101; A01N
51/00 20130101; A01N 53/00 20130101; A01N 2300/00 20130101 |
Class at
Publication: |
504/100 ;
514/378; 514/340; 514/229.2; 514/341; 514/30 |
International
Class: |
A01N 43/80 20060101
A01N043/80; A01N 43/50 20060101 A01N043/50; A01N 53/00 20060101
A01N053/00; A01N 43/90 20060101 A01N043/90; A61K 31/455 20060101
A61K031/455; A61K 31/5395 20060101 A61K031/5395; A61K 31/4439
20060101 A61K031/4439; A61K 31/277 20060101 A61K031/277; A61K
31/7048 20060101 A61K031/7048; A01N 43/88 20060101 A01N043/88; A01N
43/40 20060101 A01N043/40 |
Claims
1. A pesticidal mixture comprising 1) at least one isoxazoline
compound I of formula I: ##STR00018## wherein A is ##STR00019## and
wherein # denotes the bond in formula I; R.sup.1, R.sup.3 are
independently from one another selected from the group consisting
of hydrogen, chloro and CF.sub.3; R.sup.2 is hydrogen or chloro;
R.sup.4 is hydrogen or CH.sub.3, R.sup.5 is hydrogen, or R.sup.4
and R.sup.5 are together a bridging 1,3-butadienyl group, which
form--together with the aromatic phenylring C they are attached
to--a naphtyl ring; or the tautomers, enantiomers, diastereomers or
salts thereof, and 2) at least one active compound II selected from
A.4 a nicotinic acteylcholine receptor agonist/antagonist selected
from the group consisting of nicotin, cartap hydrochloride,
thiocyclam and the class of neonicotinoids consisting of
acteamiprid, chlothianidin, dinotefuran, imidacloprid, nitenpyram,
spinosad (allosteric agonist), spinetoram (allosteric agonist),
thiacloprid, thiamethoxam and AKD-1022.
2. The mixture according to claim 1, wherein the substituents of
the active compound I of formula I have the following meanings: A
is A-1, A-4 or A-6; R.sup.1, R.sup.3 are independently from one
another selected from the group consisting of hydrogen, chloro and
CF.sub.3; R.sup.2 is hydrogen or chloro; R.sup.4 is hydrogen or
CH.sub.3, R.sup.5 is hydrogen or R.sup.4 and R.sup.5 are together a
bridging 1,3-butadienyl group, which form--together with the
aromatic phenylring C they are attached to--a naphtyl ring; or the
tautomers, enantiomers, diastereomers or salts thereof.
3. The mixture according to claim 1, wherein the substituents of
the active compound I of formula I have the following meanings: A
is A-1, A-4 or A-6; R.sup.1, R.sup.2, R.sup.3 are chloro; R.sup.4
is hydrogen or CH.sub.3, R.sup.5 is hydrogen or R.sup.4 and R.sup.5
are together a bridging 1,3-butadienyl group, which form--together
with the aromatic phenylring C they are attached to--a naphtyl
ring; or the tautomers, enantiomers, diastereomers or salts
thereof.
4. The mixture according to claim 1, wherein the substituents of
the active compound I of formula I have the following meanings: A
is A-1, A-4 or A-6; R.sup.1, R.sup.3 are chloro; R.sup.2 is
hydrogen; R.sup.4 is hydrogen or CH.sub.3, R.sup.5 is hydrogen or
R.sup.4 and R.sup.5 are together a bridging 1,3-butadienyl group,
which form--together with the aromatic phenylring C they are
attached to--a naphtyl ring; or the tautomers, enantiomers,
diastereomers or salts thereof.
5. The mixture according to claim 1, wherein the substituents of
the active compound I of formula I have the following meanings: A
is A-1, A-4 or A-6; R.sup.1, R.sup.3 are CF.sub.3; R.sup.2 is
hydrogen; R.sup.4 is hydrogen or CH.sub.3, R.sup.5 is hydrogen or
R.sup.4 and R.sup.5 are together a bridging 1,3-butadienyl group,
which form--together with the aromatic phenylring C they are
attached to--a naphtyl ring; or the tautomers, enantiomers,
diastereomers or salts thereof.
6. The mixture according to claim 1, wherein the substituents of
the active compound I of formula I have the following meanings: A
is A-1, A-4 or A-6; R.sup.1 is CF.sub.3; R.sup.2, R.sup.3 are
hydrogen; R.sup.4 is hydrogen or CH.sub.3, R.sup.5 is hydrogen or
R.sup.4 and R.sup.5 are together a bridging 1,3-butadienyl group,
which form--together with the aromatic phenylring C they are
attached to--a naphtyl ring; or the tautomers, enantiomers,
diastereomers or salts thereof.
7. The mixture according to claim 1, wherein at least one active
compound II is selected within group A.4 from thiocyclam,
actamiprid, chlothianidin, dinotefuran, imidacloprid, nitenpyram,
thiacloprid, thiamethoxam, AKD-1022 or spinosad.
8. The mixture according to claim 1, wherein at least one active
compound II is clothianidin, imidacloprid or thiamethoxam.
9. The mixture according to claim 1, comprising the active compound
I of the formula I and the active compound II in a weight ratio of
from 500:1 to 1:100.
10. A method for protecting plants from attack or infestation by
insects, acarids or nematodes comprising contacting the plant, or
the soil or water in which the plant is growing, with a mixture
according to claim 1 in pesticidally effective amounts.
11. A method for controlling insects, arachnids or nematodes
comprising contacting an insect, acarid or nematode or their food
supply, habitat, breeding grounds or their locus with a mixture
according to claim 1 in pesticidally effective amounts.
12. A method as claimed in claim 10 or 11, wherein the mixture
according claim 1 is applied in an amount of from 5 g/ha to 2000
g/ha.
13. A method for protection of plant propagation material
comprising contacting the plant propagation material with a mixture
of claim 1 in pesticidally effective amounts.
14. A method according to claim 13 wherein the mixture is applied
in an amount of from 0.1 g to 10 kg per 100 kg of plant propagation
material.
15. A method as claimed in claim 13, wherein the plant propagation
material is/are seed(s).
16. A seed treated with the mixture according to claim 1 in an
amount of from 0.1 g to 10 kg per 100 kg of seeds.
17. A method for protecting animals against infestation or
infection by parasites which comprises administering to the animals
a parasitically effective amount of a mixture according to claim 1
to the animal in need thereof.
18. A method for treating animals infested or infected by parasites
which comprises administering to the animals a parasitically
effective amount of a mixture according claim 1 to the animal in
need thereof.
19. A method as claimed in claim 10 wherein the active compounds I
of formula I and the active compounds II are applied
simultaneously, that is jointly or separately, or in
succession.
20. A pesticidal or parasiticidal composition, comprising a liquid
or solid carrier and a mixture according to claim 1.
Description
[0001] This application is a divisional of U.S. patent application
Ser. No. 13/003,037, filed Jan. 7, 2011, which is a National Stage
application of International Application No. PCT/EP2009/058517,
filed Jul. 6, 2009, which claims the benefit of U.S. Provisional
Application No. 61/079,318, filed Jul. 9, 2008, the entire contents
of which are hereby incorporated herein by reference.
[0002] The present invention relates to mixtures of active
ingredients having synergistically enhanced action and to methods
comprising applying said mixtures.
[0003] One typical problem arising in the field of pest control
lies in the need to reduce the dosage rates of the active
ingredient in order to reduce or avoid unfavorable environmental or
toxicological effects whilst still allowing effective pest
control.
[0004] Another problem encountered concerns the need to have
available pest control agents which are effective against a broad
spectrum of pests.
[0005] There also exists the need for pest control agents that
combine know-down activity with prolonged control, that is, fast
action with long lasting action.
[0006] Another difficulty in relation to the use of pesticides is
that the repeated and exclusive application of an individual
pesticidal compound leads in many cases to a rapid selection of
pests which have developed natural or adapted resistance against
the active compound in question. Therefore there is a need for pest
control agents that help prevent or overcome resistance.
[0007] It was therefore an object of the present invention to
provide pesticidal mixtures which solves at least one of the
discussed problems as reducing the dosage rate, enhancing the
spectrum of activity or combining know-down activity with prolonged
control or as to resistance management.
[0008] We have found that this object is in part or in whole
achieved by the combination of active compounds defined below.
[0009] The present invention relates to pesticidal mixtures
comprising as active compounds [0010] 1) at least one isoxazoline
compound I of formula I:
[0010] ##STR00002## [0011] wherein [0012] A is selected from
[0012] ##STR00003## [0013] and wherein # denotes the bond in
formula I; [0014] R.sup.1, R.sup.3 are independently from one
another selected from hydrogen, chloro or CF.sub.3; [0015] R.sup.2
is hydrogen or chloro; [0016] R.sup.4 is hydrogen or CH.sub.3,
[0017] R.sup.5 is hydrogen, or [0018] R.sup.4 and R.sup.5 are
together a bridging 1,3-butadienyl group, which form--together with
the aromatic phenylring C they are attached to--a naphtyl ring;
[0019] or the tautomers, enantiomers, diastereomers or salts
thereof, [0020] and [0021] 2) at least one active compound II
selected from group A consisting of [0022] A.1 Acetylcholine
esterase inhibitors selected from triazemate or from the class of
carbamates consisting of aldicarb, alanycarb, benfuracarb,
carbaryl, carbofuran, carbosulfan, methiocarb, methomyl, oxamyl,
primicarb, propoxur and thiodicarb or from the class of
organophosphates consisting of acephate, azinphos-ethyl,
azinphos-methyl, chlorfenvinphos, chlorpyrifos,
chlorpyrifos-methyl, demeton-S-methyl, diazinon, dichlorvos/DDVP,
dicrotophos, dimethoate, disulfoton, ethion, fenitrothion,
fenthion, isoxathion, malathion, methamidaphos, methidathion,
mevinphos, monocrotophos, oxymethoate, oxydemeton-methyl,
parathion, parathion-methyl, phenthoate, phorate, phosalone,
phosmet, phosphamidon, pirimiphos-methyl, quinalphos, terbufos,
tetrachlorvinphos, triazophos and trichlorfon; [0023] A.2
GABA-gated chloride channel antagonists selected from the
cyclodiene organochlorine endosulfan, from
N-Ethyl-2,2-dimethylpropionamide-2-(2,6-dichloro-.alpha...alpha...alpha.--
trifluoro-p-tolyl) hydrazon or
N-Ethyl-2,2-dichloro-1-methylcyclopropane-carboxamide-2-(2,6-dichloro-.al-
pha...alpha...alpha.-trifluoro-p-tolyl) hydrazon or from the class
of phenylpyrazoles consisting of acetoprole, ethiprole, fipronil,
pyrafluprole, pyriprole, vaniliprole and the phenylpyrazole
compound II.A21:
[0023] ##STR00004## [0024] A.3 Sodium channel modulators selected
from the class of pyrethroids consisiting of allethrin, bifenthrin,
beta-cyfluthrin, cyfluthrin, lambda-cyhalothrin, cypermethrin,
alpha-cypermethrin, beta-cypermethrin, zeta-cypermethrin,
deltamethrin, esfenvalerate, etofenprox, fenpropathrin,
fenvalerate, flucythrinate, metofluthrin, permethrin, profluthrin,
pyrethrin (pyrethrum), tau-fluvalinate, silafluofen and
tralomethrin; [0025] A.4 Nicotinic acteylcholine receptor
agonists/antagonists selected from nicotin, cartap hydrochloride or
thiocyclam or selected from the class of neonicotinoids consisting
of acteamiprid, chlothianidin, dinotefuran, imidacloprid,
nitenpyram, spinosad (allosteric agonist), spinetroam (allosteric
agonist), thiacloprid, thiamethoxam and AKD-1022; [0026] A.5
Chloride channel activators selected from abamectin, emamectin
benzoate, lepimectin or milbemectin; [0027] A.6 Juvenile hormone
mimics selected from hydroprene, kinoprene, fenoxycarb or
pyriproxyfen; [0028] A.7 Compounds affecting the oxidative
phosphorylation selected from diafenthiuron, fenbutatin oxide,
propargite or chlorfenapyr; [0029] A.8 Inhibitors of the chitin
biosynthesis selected from buprofezin or from the class of
benzylureas consisting of bistrifluron, diflubenzuron,
flufenoxuron, hexaflumuron, lufenuron, novaluron or teflubenzuron;
[0030] A.9 Moulting disruptors selected from cyromazine or from the
class of ecdysone agonists consisting of methoxyfenozide,
tebufenozide and azadirachtin; [0031] A.10 Mitochondrial electron
transport inhibitors selected from pyridaben, tolfenpyrad or
flufenerim. [0032] A.11 Voltage-dependent sodium channel blockers
selected from indoxacarb or metaflumizone. [0033] A.12 Inhibitors
of the lipid synthesis selected from spirodiclofen, spiromesifen or
spirotetramat. [0034] A.13 A group of various compounds consisting
of amidoflumet, amitraz, bifenazate, clofentezine, cyenopyrafen,
cyflumetofen, etoxazole, flonicamid, flubendiamine, flupyrazophos,
hexythiazox, piperonyl butoxide, pymetrozine, pyridalyl,
pyrifluquinazon, chlorantraniliprole and the anthranilamid compound
II.A.sup.13.1:
[0034] ##STR00005## [0035] and the anthranilamid compounds [0036]
5-Bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazole-3-carboxylic acid
[4-cyano-2-(1-cyclopropyl-ethylcarbamoyl)-6-methyl-phenyl]-amide,
[0037] 5-Bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazole-3-carboxylic
acid
[2-chloro-4-cyano-6-(1-cyclopropyl-ethylcarbamoyl)-phenyl]-amide,
[0038] 5-Bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazole-3-carboxylic
acid
[2-bromo-4-cyano-6-(1-cyclopropyl-ethylcarbamoyl)-phenyl]-amide,
[0039] 5-Bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazole-3-carboxylic
acid
[2-bromo-4-chloro-6-(1-cyclopropyl-ethylcarbamoyl)-phenyl]-amide,
[0040] 5-Bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazole-3-carboxylic
acid [2,4-dichloro-6-(1-cyclopropyl-ethylcarbamoyl)-phenyl]-amide,
[0041] 5-Bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazole-3-carboxylic
acid
[4-chloro-2-(1-cyclopropyl-ethylcarbamoyl)-6-methyl-phenyl]-amide,
[0042]
N'-(2-{[5-Bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazole-3-carbonyl]-amino}--
5-chloro-3-methyl-benzoyl)-hydrazinecarboxylic acid methyl ester,
[0043]
N'-(2-{[5-Bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazole-3-carbonyl]-amino}--
5-chloro-3-methyl-benzoyl)-N'-methyl-hydrazinecarboxylic acid
methyl ester, [0044]
N'-(2-{[5-Bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazole-3-carbonyl]-amino}--
5-chloro-3-methyl-benzoyl)-N,N'-dimethyl-hydrazinecarboxylic acid
methyl ester, [0045]
N'-(3,5-Dibromo-2-{[5-bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazole-3-carbo-
nyl]-amino}-benzoyl)-hydrazinecarboxylic acid methyl ester, [0046]
N'-(3,5-Dibromo-2-{[5-bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazole-3-carbo-
nyl]-amino}-benzoyl)-N'-methyl-hydrazinecarboxylic acid methyl
ester and [0047]
N'-(3,5-Dibromo-2-{[5-bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazole--
3-carbonyl]-amino}-benzoyl)-N,N'-dimethyl-hydrazinecarboxylic acid
methyl ester, the aminofuranone compounds [0048]
4-{[(6-Bromopyrid-3-yl)methyl](2-fluoroethyl)amino}furan-2(5H)-on,
[0049]
4-{[(6-Fluoropyrid-3-yl)methyl](2,2-difluoroethyl)amino}furan-2(5H)-on,
[0050]
4-{[(2-Chloro1,3-thiazolo-5-yl)methyl](2-fluoroethyl)amino}furan-2-
(5H)-on, [0051]
4-{[(6-Chloropyrid-3-yl)methyl](2-fluoroethyl)amino}furan-2(5H)-on,
[0052]
4-{[(6-Chloropyrid-3-yl)methyl](2,2-difluoroethyl)amino}furan-2(5H-
)-on, [0053]
4-{[(6-Chloro-5-fluoropyrid-3-yl)methyl](methyl)amino}furan-2(5H)-on,
[0054]
4-{[(5,6-Dichloropyrid-3-yl)methyl](2-fluoroethyl)amino}furan-2(5H-
)-on, [0055]
4-{[(6-Chloro-5-fluoropyrid-3-yl)methyl](cyclopropyl)amino}furan-2(5H)-on-
, [0056]
4-{[(6-Chloropyrid-3-yl)methyl](cyclopropyl)amino}furan-2(5H)-on
and [0057]
4-{[(6-Chloropyrid-3-yl)methyl](methyl)amino}furan-2(5H)-on, the
malononitrile compounds
2-(2,2,3,3,4,4,5,5-octafluoropentyl)-2-(3,3,3-trifluoropropyl)malononitri-
le
(CF.sub.2H--CF.sub.2--CF.sub.2--CF.sub.2--CH.sub.2--C(CN).sub.2--CH.sub-
.2--CH.sub.2--CF.sub.3) and
2-(2,2,3,3,4,4,5,5-octafluoropentyl)-2-(3,3,4,4,4-pentafluorobutyl)-malon-
odinitrile
(CF.sub.2H--CF.sub.2--CF.sub.2--CF.sub.2--CH.sub.2--C(CN).sub.2-
--CH.sub.2--CH.sub.2--CF.sub.2--CF.sub.3), the alkynylether
compound
4-But-2-ynyloxy-6-(3,5-dimethyl-piperidin-1-yl)-2-fluoro-pyrimidine,
the sulfoximine compounds II.A.sup.13.2
[0057] ##STR00006## [0058] and II.A.sup.13.4
[0058] ##STR00007## [0059] the phtalamid compound (R)-,
(S)-3-Chlor-N1-{2-methyl-4-[1,2,2,2-tetrafluor-1-(trifluormethyl)ethyl]ph-
enyl}-N2-(1-methyl-2-methylsulfonylethyl)phthalamid
(II.A.sup.13.5), the pyripyropene compound Cyclopropaneacetic acid,
1,1'-[(3
S,4R,4aR,6S,6aS,12R,12aS,12bS)-4-[[(2-cyclopropylacetyl)oxy]methyl]-1,3,4-
,4a,5,6,6a,12,12a,12b-decahydro-12-hydroxy-4,6a,12b-trimethyl-11-oxo-9-(3--
pyridinyl)-2H,11H-naphtho[2,1-b]pyrano[3,4-e]pyran-3,6-diyl]ester
(II.A.sup.13.6) and the pyridazine compound
8-(2-Cyclopropylmethoxy-4-trifluoromethyl-phenoxy)-3-(6-trifluoromethyl-p-
yridazin-3-yl)-3-aza-bicyclo[3.2.1]octane (II.A.sup.13.7) [0060] in
synergistically effective amounts.
[0061] Moreover, we have found that simultaneous, that is joint or
separate, application of one ore more active compound I and one or
more compounds II or successive application of one or more active
compound I and one or more active compounds II allows enhanced
control of pests compared to the control rates that are possible
with the individual compounds.
[0062] The present invention also provides methods for the control
of insects, acarids or nematodes comprising contacting the insect,
acarid or nematode or their food supply, habitat, breeding grounds
or their locus with a pesticidally effective amount of mixtures of
at least one active compound I with at least one active compound
II.
[0063] Moreover, the present invention also relates to a method of
protecting plants from attack or infestation by insects, acarids or
nematodes comprising contacting the plant, or the soil or water in
which the plant is growing, with a pesticidally effective amount of
a mixture of at least one active compound I with at least one
active compound II.
[0064] The invention also provides a method for the protection of
seeds from soil insects and of the seedlings' roots and shoots from
soil and foliar insects which comprises contacting the seeds before
sowing and/or after pregermination with a pesticidally effective
amount of a mixture of at least one active compound I with at least
one active compound II.
[0065] The invention also provides seeds comprising a mixture of at
least one active compound I with at least one active compound
II.
[0066] The invention also relates to the use of a mixture of at
least one active compound I with at least one active compound II
for combating insects, arachnids or nematodes.
[0067] The invention also provides the use of a mixture of at least
one active compound I with at least one active compound II for
combating parasites in and on animals.
[0068] The invention provides further a method for treating,
controlling, preventing or protecting animals against infestation
or infection by parasites which comprises orally, topically or
parenterally administering or applying to the animals a
parasiticidally effective amount of a mixture of at least one
active compound I with at least one active compound II.
[0069] Another aspect of the present invention is a process for the
preparation of a composition for treating, controlling, preventing
or protecting animals against infestation or infection by parasites
which comprises a parasiticidally effective amount of a mixture of
the active compound I with at least one active compound II.
[0070] Pesticidal active isoxazoline compounds have been described
in WO05/085219, WO2007/075459, WO2008/019760 and WO2008/012027.
Further isoxazoline compounds comprising annelated bicyclic
moieties, as an naphtyl group, are disclosed in WO2007/079162.
Preparation methods are described in WO 2007/074789 and WO
2007/094313. In general, pesticidal active isoaxzoline compounds
are also described in JP 2007/016017, JP 2007/106756, WO
2005/085216, WO 2007/026965, WO 2007/105814, WO 2007/125984 WO
2007/026965, JP 2008-239611, WO 2008108448, WO 2009/005015, WO
2009/035004, WO 2008/150393, WO 2008/154528, WO 2009/002809, WO
2009/003075, WO 2009/025983, WO 2009/051956, WO 2009/022746, WO
2009/049846, WO 2008/126665, US 2008/00262057 and WO
2009/024541.
[0071] The prior art does not disclose pesticidal mixtures
comprising selective isoxazoline compounds according to the present
invention showing unexpected and synergistic effects in combination
with other pesticidically active compounds.
[0072] The commercially available compounds of the group A may be
found in The Pesticide Manual, 13.sup.th Edition, British Crop
Protection Council (2003) among other publications. Thiamides
derivatives in analogy of formula II.A.sup.2.1 and their
preparation have been described in WO 98/28279. Lepimectin is known
from Agro Project, PJB Publications Ltd, November 2004.
Methidathion and Paraoxon and their preparation have been described
in Farm Chemicals Handbook, Volume 88, Meister Publishing Company,
2001. Acetoprole and its preparation have been described in WO
98/28277. Metaflumizone and its preparation have been described in
EP-A1 462 456. Flupyrazofos has been described in Pesticide Science
54, 1988, p. 237-243 and in U.S. Pat. No. 4,822,779. Pyrafluprole
and its preparation have been described in JP-A 2002-193709 and in
WO 01/00614. Pyriprole and its preparation have been described in
WO 98/45274 and in U.S. Pat. No. 6,335,357. Amidoflumet and its
preparation have been described in U.S. Pat. No. 6,221,890 and in
JP-A 21010907. Flufenerim and its preparation have been described
in WO 03/007717 and in WO 03/007718. Cyflumetofen and its
preparation have been described in WO 04/080180. Preparation
methods for neonicotionids similar to AKD-1022 have been described
by Zhang, A. et al. in J. Neurochemistry, 75(3), 2000.
Anthranilamides like chloranthraniliprole and derivatives in
analogy of formula II.A.sup.13.1 and their preparation have been
described in WO 01/70671; WO 02/48137; WO 03/24222, WO 03/15518, WO
03/15519, WO 04/67528; WO 04/33468 and WO 05/118552. Further
anthranilamides have also been described in WO 2008/72743, WO
200872783 and WO 2007/043677. Malononitrile compounds have been
described e.g. in WO 02/089579, WO 02/090320, WO 02/090321, WO
04/006677, WO 05/068423, WO 05/068432 and WO 05/063694. The
alkynylether compound is described e.g. in JP 2006131529.
Sulfoximine derivatives of and in analogy of formulae
II.A.sup.13.2, II.A.sup.13.3 or II.A.sup.13.4 and their
preparations have been described in WO 2006/060029. The phthalamide
compound (II..sup.A13.5) is known from WO 2007/101540 The
aminofuranone compounds have been described eg. in WO 2007/115644.
The pyripyropene derivative (II.A.sup.13.6) has been described in
WO 2008/66153 and WO 2008/108491. The pyridazin compound
(II.A.sup.13.2) has been described in JP 2008/115155.
Preferences
Preferred Compounds I of Formula I
[0073] With regard to their use in the pesticidal mixtures of the
present invention, compounds I of formula I are preferred, wherein
[0074] A is A-1, A-4 or A-6; [0075] R.sup.1, R.sup.3 are
independently from one another selected from hydrogen, chloro or
CF.sub.3; [0076] R.sup.2 is hydrogen or chloro; [0077] R.sup.4 is
hydrogen oder CH.sub.3,
[0078] R.sup.5 is hydrogen or [0079] R.sup.4 and R.sup.5 are
together a bridging 1,3-butadienyl group, which form--together with
the aromatic phenylring C they are attached to--a naphtyl ring;
[0080] Especially preferred are compounds I of formula I having the
following meanings: [0081] A is A-1, A-4 or A-6; [0082] R.sup.1,
R.sup.2, R.sup.3 are chloro; [0083] R.sup.4 is hydrogen oder
CH.sub.3, [0084] R.sup.5 is hydrogen or [0085] R.sup.4 and R.sup.5
are together a bridging 1,3-butadienyl group, which form--together
with the aromatic phenylring C they are attached to--a naphtyl
ring;
[0086] Especially preferred are compounds I of formula I having the
following meanings: [0087] A is A-1, A-4 or A-6; [0088] R.sup.1,
R.sup.3 are chloro; [0089] R.sup.2 is hydrogen; [0090] R.sup.4 is
hydrogen oder CH.sub.3, [0091] R.sup.5 is hydrogen or [0092]
R.sup.4 and R.sup.5 are together a bridging 1,3-butadienyl group,
which form--together with the aromatic phenylring C they are
attached to--a naphtyl ring;
[0093] Further preferred are compounds I of formula I having the
following meanings: [0094] A is A-1, A-4 or A-6; [0095] R.sup.1,
R.sup.3 are CF.sub.3; [0096] R.sup.2 is hydrogen; [0097] R.sup.4 is
hydrogen oder CH.sub.3, [0098] R.sup.5 is hydrogen or [0099]
R.sup.4 and R.sup.5 are together a bridging 1,3-butadienyl group,
which form--together with the aromatic phenylring C they are
attached to--a naphtyl ring; [0100] or [0101] A is A-1, A-4 or A-6;
[0102] R.sup.1 is CF.sub.3; [0103] R.sup.2, R.sup.3 are hydrogen;
[0104] R.sup.4 is hydrogen oder CH.sub.3, [0105] R.sup.5 is
hydrogen or [0106] R.sup.4 and R.sup.5 are together a bridging
1,3-butadienyl group, which form--together with the aromatic
phenylring C they are attached to--a naphtyl ring;
[0107] Compound I examples of isoxazoline compounds of formula I
are given in the following table C.I.1:
TABLE-US-00001 TABLE C.I.1 Compound I A R.sup.1 R.sup.2 R.sup.3
R.sup.4 R.sup.5 C.I-1 A-1 H H H H H C.I-2 A-2 H H H H H C.I-3 A-3 H
H H H H C.I-4 A-4 H H H H H C.I-5 A-5 H H H H H C.I-6 A-6 H H H H H
C.I-7 A-7 H H H H H C.I-8 A-8 H H H H H C.I-9 A-9 H H H H H C.I-10
A-1 H Cl H H H C.I-11 A-2 H Cl H H H C.I-12 A-3 H Cl H H H C.I-13
A-4 H Cl H H H C.I-14 A-5 H Cl H H H C.I-15 A-6 H Cl H H H C.I-16
A-7 H Cl H H H C.I-17 A-8 H Cl H H H C.I-18 A-9 H Cl H H H C.I-19
A-1 Cl H H H H C.I-20 A-2 Cl H H H H C.I-21 A-3 Cl H H H H C.I-22
A-4 Cl H H H H C.I-23 A-5 Cl H H H H C.I-24 A-6 Cl H H H H C.I-25
A-7 Cl H H H H C.I-26 A-8 Cl H H H H C.I-27 A-9 Cl H H H H C.I-28
A-1 Cl Cl H H H C.I-29 A-2 Cl Cl H H H C.I-30 A-3 Cl Cl H H H
C.I-31 A-4 Cl Cl H H H C.I-32 A-5 Cl Cl H H H C.I-33 A-6 Cl Cl H H
H C.I-34 A-7 Cl Cl H H H C.I-35 A-8 Cl Cl H H H C.I-36 A-9 Cl Cl H
H H C.I-37 A-1 CF.sub.3 H H H H C.I-38 A-2 CF.sub.3 H H H H C.I-39
A-3 CF.sub.3 H H H H C.I-40 A-4 CF.sub.3 H H H H C.I-41 A-5
CF.sub.3 H H H H C.I-42 A-6 CF.sub.3 H H H H C.I-43 A-7 CF.sub.3 H
H H H C.I-44 A-8 CF.sub.3 H H H H C.I-45 A-9 CF.sub.3 H H H H
C.I-46 A-1 CF.sub.3 Cl H H H C.I-47 A-2 CF.sub.3 Cl H H H C.I-48
A-3 CF.sub.3 Cl H H H C.I-49 A-4 CF.sub.3 Cl H H H C.I-50 A-5
CF.sub.3 Cl H H H C.I-51 A-6 CF.sub.3 Cl H H H C.I-52 A-7 CF.sub.3
Cl H H H C.I-53 A-8 CF.sub.3 Cl H H H C.I-54 A-9 CF.sub.3 Cl H H H
C.I-55 A-1 H H Cl H H C.I-56 A-2 H H Cl H H C.I-57 A-3 H H Cl H H
C.I-58 A-4 H H Cl H H C.I-59 A-5 H H Cl H H C.I-60 A-6 H H Cl H H
C.I-61 A-7 H H Cl H H C.I-62 A-8 H H Cl H H C.I-63 A-9 H H Cl H H
C.I-64 A-1 H Cl Cl H H C.I-65 A-2 H Cl Cl H H C.I-66 A-3 H Cl Cl H
H C.I-67 A-4 H Cl Cl H H C.I-68 A-5 H Cl Cl H H C.I-69 A-6 H Cl Cl
H H C.I-70 A-7 H Cl Cl H H C.I-71 A-8 H Cl Cl H H C.I-72 A-9 H Cl
Cl H H C.I-73 A-1 Cl H Cl H H C.I-74 A-2 Cl H Cl H H C.I-75 A-3 Cl
H Cl H H C.I-76 A-4 Cl H Cl H H C.I-77 A-5 Cl H Cl H H C.I-78 A-6
Cl H Cl H H C.I-79 A-7 Cl H Cl H H C.I-80 A-8 Cl H Cl H H C.I-81
A-9 Cl H Cl H H C.I-82 A-1 Cl Cl Cl H H C.I-83 A-2 Cl Cl Cl H H
C.I-84 A-3 Cl Cl Cl H H C.I-85 A-4 Cl Cl Cl H H C.I-86 A-5 Cl Cl Cl
H H C.I-87 A-6 Cl Cl Cl H H C.I-88 A-7 Cl Cl Cl H H C.I-89 A-8 Cl
Cl Cl H H C.I-90 A-9 Cl Cl Cl H H C.I-91 A-1 CF.sub.3 H Cl H H
C.I-92 A-2 CF.sub.3 H Cl H H C.I-93 A-3 CF.sub.3 H Cl H H C.I-94
A-4 CF.sub.3 H Cl H H C.I-95 A-5 CF.sub.3 H Cl H H C.I-96 A-6
CF.sub.3 H Cl H H C.I-97 A-7 CF.sub.3 H Cl H H C.I-98 A-8 CF.sub.3
H Cl H H C.I-99 A-9 CF.sub.3 H Cl H H C.I-100 A-1 CF.sub.3 Cl Cl H
H C.I-101 A-2 CF.sub.3 Cl Cl H H C.I-102 A-3 CF.sub.3 Cl Cl H H
C.I-103 A-4 CF.sub.3 Cl Cl H H C.I-104 A-5 CF.sub.3 Cl Cl H H
C.I-105 A-6 CF.sub.3 Cl Cl H H C.I-106 A-7 CF.sub.3 Cl Cl H H
C.I-107 A-8 CF.sub.3 Cl Cl H H C.I-108 A-9 CF.sub.3 Cl Cl H H
C.I-109 A-1 H H CF.sub.3 H H C.I-110 A-2 H H CF.sub.3 H H C.I-111
A-3 H H CF.sub.3 H H C.I-112 A-4 H H CF.sub.3 H H C.I-113 A-5 H H
CF.sub.3 H H C.I-114 A-6 H H CF.sub.3 H H C.I-115 A-7 H H CF.sub.3
H H C.I-116 A-8 H H CF.sub.3 H H C.I-117 A-9 H H CF.sub.3 H H
C.I-118 A-1 H Cl CF.sub.3 H H C.I-119 A-2 H Cl CF.sub.3 H H C.I-120
A-3 H Cl CF.sub.3 H H C.I-121 A-4 H Cl CF.sub.3 H H C.I-122 A-5 H
Cl CF.sub.3 H H C.I-123 A-6 H Cl CF.sub.3 H H C.I-124 A-7 H Cl
CF.sub.3 H H C.I-125 A-8 H Cl CF.sub.3 H H C.I-126 A-9 H Cl
CF.sub.3 H H C.I-127 A-1 Cl H CF.sub.3 H H C.I-128 A-2 Cl H
CF.sub.3 H H C.I-129 A-3 Cl H CF.sub.3 H H C.I-130 A-4 Cl H
CF.sub.3 H H C.I-131 A-5 Cl H CF.sub.3 H H C.I-132 A-6 Cl H
CF.sub.3 H H C.I-133 A-7 Cl H CF.sub.3 H H C.I-134 A-8 Cl H
CF.sub.3 H H C.I-135 A-9 Cl H CF.sub.3 H H C.I-136 A-1 Cl Cl
CF.sub.3 H H C.I-137 A-2 Cl Cl CF.sub.3 H H C.I-138 A-3 Cl Cl
CF.sub.3 H H C.I-139 A-4 Cl Cl CF.sub.3 H H C.I-140 A-5 Cl Cl
CF.sub.3 H H C.I-141 A-6 Cl Cl CF.sub.3 H H C.I-142 A-7 Cl Cl
CF.sub.3 H H C.I-143 A-8 Cl Cl CF.sub.3 H H C.I-144 A-9 Cl Cl
CF.sub.3 H H C.I-145 A-1 CF.sub.3 H CF.sub.3 H H C.I-146 A-2
CF.sub.3 H CF.sub.3 H H C.I-147 A-3 CF.sub.3 H CF.sub.3 H H C.I-148
A-4 CF.sub.3 H CF.sub.3 H H C.I-149 A-5 CF.sub.3 H CF.sub.3 H H
C.I-150 A-6 CF.sub.3 H CF.sub.3 H H C.I-151 A-7 CF.sub.3 H CF.sub.3
H H C.I-152 A-8 CF.sub.3 H CF.sub.3 H H C.I-153 A-9 CF.sub.3 H
CF.sub.3 H H C.I-154 A-1 CF.sub.3 Cl CF.sub.3 H H C.I-155 A-2
CF.sub.3 Cl CF.sub.3 H H C.I-156 A-3 CF.sub.3 Cl CF.sub.3 H H
C.I-157 A-4 CF.sub.3 Cl CF.sub.3 H H C.I-158 A-5 CF.sub.3 Cl
CF.sub.3 H H C.I-159 A-6 CF.sub.3 Cl CF.sub.3 H H C.I-160 A-7
CF.sub.3 Cl CF.sub.3 H H C.I-161 A-8 CF.sub.3 Cl CF.sub.3 H H
C.I-162 A-9 CF.sub.3 Cl CF.sub.3 H H C.I-163 A-1 H H H CH.sub.3 H
C.I-164 A-2 H H H CH.sub.3 H C.I-165 A-3 H H H CH.sub.3 H C.I-166
A-4 H H H CH.sub.3 H C.I-167 A-5 H H H CH.sub.3 H C.I-168 A-6 H H H
CH.sub.3 H C.I-169 A-7 H H H CH.sub.3 H C.I-170 A-8 H H H CH.sub.3
H C.I-171 A-9 H H H CH.sub.3 H C.I-172 A-1 H Cl H CH.sub.3 H
C.I-173 A-2 H Cl H CH.sub.3 H C.I-174 A-3 H Cl H CH.sub.3 H C.I-175
A-4 H Cl H CH.sub.3 H C.I-176 A-5 H Cl H CH.sub.3 H C.I-177 A-6 H
Cl H CH.sub.3 H C.I-178 A-7 H Cl H CH.sub.3 H C.I-179 A-8 H Cl H
CH.sub.3 H C.I-180 A-9 H Cl H CH.sub.3 H C.I-181 A-1 Cl H H
CH.sub.3 H C.I-182 A-2 Cl H H CH.sub.3 H C.I-183 A-3 Cl H H
CH.sub.3 H C.I-184 A-4 Cl H H CH.sub.3 H C.I-185 A-5 Cl H H
CH.sub.3 H C.I-186 A-6 Cl H H CH.sub.3 H C.I-187 A-7 Cl H H
CH.sub.3 H C.I-188 A-8 Cl H H CH.sub.3 H C.I-189 A-9 Cl H H
CH.sub.3 H C.I-190 A-1 Cl Cl H CH.sub.3 H C.I-191 A-2 Cl Cl H
CH.sub.3 H C.I-192 A-3 Cl Cl H CH.sub.3 H C.I-193 A-4 Cl Cl H
CH.sub.3 H C.I-194 A-5 Cl Cl H CH.sub.3 H C.I-195 A-6 Cl Cl H
CH.sub.3 H C.I-196 A-7 Cl Cl H CH.sub.3 H C.I-197 A-8 Cl Cl H
CH.sub.3 H C.I-198 A-9 Cl Cl H CH.sub.3 H C.I-199 A-1 CF.sub.3 H H
CH.sub.3 H C.I-200 A-2 CF.sub.3 H H CH.sub.3 H C.I-201 A-3 CF.sub.3
H H CH.sub.3 H C.I-202 A-4 CF.sub.3 H H CH.sub.3 H C.I-203 A-5
CF.sub.3 H H CH.sub.3 H C.I-204 A-6 CF.sub.3 H H CH.sub.3 H C.I-205
A-7 CF.sub.3 H H CH.sub.3 H C.I-206 A-8 CF.sub.3 H H CH.sub.3 H
C.I-207 A-9 CF.sub.3 H H CH.sub.3 H C.I-208 A-1 CF.sub.3 Cl H
CH.sub.3 H C.I-209 A-2 CF.sub.3 Cl H CH.sub.3 H C.I-210 A-3
CF.sub.3 Cl H CH.sub.3 H C.I-211 A-4 CF.sub.3 Cl H CH.sub.3 H
C.I-212 A-5 CF.sub.3 Cl H CH.sub.3 H C.I-213 A-6 CF.sub.3 Cl H
CH.sub.3 H C.I-214 A-7 CF.sub.3 Cl H CH.sub.3 H C.I-215 A-8
CF.sub.3 Cl H CH.sub.3 H C.I-216 A-9 CF.sub.3 Cl H CH.sub.3 H
C.I-217 A-1 H H Cl CH.sub.3 H C.I-218 A-2 H H Cl CH.sub.3 H C.I-219
A-3 H H Cl CH.sub.3 H C.I-220 A-4 H H Cl CH.sub.3 H C.I-221 A-5 H H
Cl CH.sub.3 H C.I-222 A-6 H H Cl CH.sub.3 H C.I-223 A-7 H H Cl
CH.sub.3 H C.I-224 A-8 H H Cl CH.sub.3 H C.I-225 A-9 H H Cl
CH.sub.3 H C.I-226 A-1 H Cl Cl CH.sub.3 H C.I-227 A-2 H Cl Cl
CH.sub.3 H C.I-228 A-3 H Cl Cl CH.sub.3 H C.I-229 A-4 H Cl Cl
CH.sub.3 H C.I-230 A-5 H Cl Cl CH.sub.3 H C.I-231 A-6 H Cl Cl
CH.sub.3 H C.I-232 A-7 H Cl Cl CH.sub.3 H C.I-233 A-8 H Cl Cl
CH.sub.3 H C.I-234 A-9 H Cl Cl CH.sub.3 H C.I-235 A-1 Cl H Cl
CH.sub.3 H C.I-236 A-2 Cl H Cl CH.sub.3 H C.I-237 A-3 Cl H Cl
CH.sub.3 H C.I-238 A-4 Cl H Cl CH.sub.3 H C.I-239 A-5 Cl H Cl
CH.sub.3 H C.I-240 A-6 Cl H Cl CH.sub.3 H C.I-241 A-7 Cl H Cl
CH.sub.3 H C.I-242 A-8 Cl H Cl CH.sub.3 H C.I-243 A-9 Cl H Cl
CH.sub.3 H C.I-244 A-1 Cl Cl Cl CH.sub.3 H C.I-245 A-2 Cl Cl Cl
CH.sub.3 H C.I-246 A-3 Cl Cl Cl CH.sub.3 H
C.I-247 A-4 Cl Cl Cl CH.sub.3 H C.I-248 A-5 Cl Cl Cl CH.sub.3 H
C.I-249 A-6 Cl Cl Cl CH.sub.3 H C.I-250 A-7 Cl Cl Cl CH.sub.3 H
C.I-251 A-8 Cl Cl Cl CH.sub.3 H C.I-252 A-9 Cl Cl Cl CH.sub.3 H
C.I-253 A-1 CF.sub.3 H Cl CH.sub.3 H C.I-254 A-2 CF.sub.3 H Cl
CH.sub.3 H C.I-255 A-3 CF.sub.3 H Cl CH.sub.3 H C.I-256 A-4
CF.sub.3 H Cl CH.sub.3 H C.I-257 A-5 CF.sub.3 H Cl CH.sub.3 H
C.I-258 A-6 CF.sub.3 H Cl CH.sub.3 H C.I-259 A-7 CF.sub.3 H Cl
CH.sub.3 H C.I-260 A-8 CF.sub.3 H Cl CH.sub.3 H C.I-261 A-9
CF.sub.3 H Cl CH.sub.3 H C.I-262 A-1 CF.sub.3 Cl Cl CH.sub.3 H
C.I-263 A-2 CF.sub.3 Cl Cl CH.sub.3 H C.I-264 A-3 CF.sub.3 Cl Cl
CH.sub.3 H C.I-265 A-4 CF.sub.3 Cl Cl CH.sub.3 H C.I-266 A-5
CF.sub.3 Cl Cl CH.sub.3 H C.I-267 A-6 CF.sub.3 Cl Cl CH.sub.3 H
C.I-268 A-7 CF.sub.3 Cl Cl CH.sub.3 H C.I-269 A-8 CF.sub.3 Cl Cl
CH.sub.3 H C.I-270 A-9 CF.sub.3 Cl Cl CH.sub.3 H C.I-271 A-1 H H
CF.sub.3 CH.sub.3 H C.I-272 A-2 H H CF.sub.3 CH.sub.3 H C.I-273 A-3
H H CF.sub.3 CH.sub.3 H C.I-274 A-4 H H CF.sub.3 CH.sub.3 H C.I-275
A-5 H H CF.sub.3 CH.sub.3 H C.I-276 A-6 H H CF.sub.3 CH.sub.3 H
C.I-277 A-7 H H CF.sub.3 CH.sub.3 H C.I-278 A-8 H H CF.sub.3
CH.sub.3 H C.I-279 A-9 H H CF.sub.3 CH.sub.3 H C.I-280 A-1 H Cl
CF.sub.3 CH.sub.3 H C.I-281 A-2 H Cl CF.sub.3 CH.sub.3 H C.I-282
A-3 H Cl CF.sub.3 CH.sub.3 H C.I-283 A-4 H Cl CF.sub.3 CH.sub.3 H
C.I-284 A-5 H Cl CF.sub.3 CH.sub.3 H C.I-285 A-6 H Cl CF.sub.3
CH.sub.3 H C.I-286 A-7 H Cl CF.sub.3 CH.sub.3 H C.I-287 A-8 H Cl
CF.sub.3 CH.sub.3 H C.I-288 A-9 H Cl CF.sub.3 CH.sub.3 H C.I-289
A-1 Cl H CF.sub.3 CH.sub.3 H C.I-290 A-2 Cl H CF.sub.3 CH.sub.3 H
C.I-291 A-3 Cl H CF.sub.3 CH.sub.3 H C.I-292 A-4 Cl H CF.sub.3
CH.sub.3 H C.I-293 A-5 Cl H CF.sub.3 CH.sub.3 H C.I-294 A-6 Cl H
CF.sub.3 CH.sub.3 H C.I-295 A-7 Cl H CF.sub.3 CH.sub.3 H C.I-296
A-8 Cl H CF.sub.3 CH.sub.3 H C.I-297 A-9 Cl H CF.sub.3 CH.sub.3 H
C.I-298 A-1 Cl Cl CF.sub.3 CH.sub.3 H C.I-299 A-2 Cl Cl CF.sub.3
CH.sub.3 H C.I-300 A-3 Cl Cl CF.sub.3 CH.sub.3 H C.I-301 A-4 Cl Cl
CF.sub.3 CH.sub.3 H C.I-302 A-5 Cl Cl CF.sub.3 CH.sub.3 H C.I-303
A-6 Cl Cl CF.sub.3 CH.sub.3 H C.I-304 A-7 Cl Cl CF.sub.3 CH.sub.3 H
C.I-305 A-8 Cl Cl CF.sub.3 CH.sub.3 H C.I-306 A-9 Cl Cl CF.sub.3
CH.sub.3 H C.I-307 A-1 CF.sub.3 H CF.sub.3 CH.sub.3 H C.I-308 A-2
CF.sub.3 H CF.sub.3 CH.sub.3 H C.I-309 A-3 CF.sub.3 H CF.sub.3
CH.sub.3 H C.I-310 A-4 CF.sub.3 H CF.sub.3 CH.sub.3 H C.I-311 A-5
CF.sub.3 H CF.sub.3 CH.sub.3 H C.I-312 A-6 CF.sub.3 H CF.sub.3
CH.sub.3 H C.I-313 A-7 CF.sub.3 H CF.sub.3 CH.sub.3 H C.I-314 A-8
CF.sub.3 H CF.sub.3 CH.sub.3 H C.I-315 A-9 CF.sub.3 H CF.sub.3
CH.sub.3 H C.I-316 A-1 CF.sub.3 Cl CF.sub.3 CH.sub.3 H C.I-317 A-2
CF.sub.3 Cl CF.sub.3 CH.sub.3 H C.I-318 A-3 CF.sub.3 Cl CF.sub.3
CH.sub.3 H C.I-319 A-4 CF.sub.3 Cl CF.sub.3 CH.sub.3 H C.I-320 A-5
CF.sub.3 Cl CF.sub.3 CH.sub.3 H C.I-321 A-6 CF.sub.3 Cl CF.sub.3
CH.sub.3 H C.I-322 A-7 CF.sub.3 Cl CF.sub.3 CH.sub.3 H C.I-323 A-8
CF.sub.3 Cl CF.sub.3 CH.sub.3 H C.I-324 A-9 CF.sub.3 Cl CF.sub.3
CH.sub.3 H C.I-325 A-1 H H H CH.dbd.CH--CH.dbd.CH C.I-326 A-2 H H H
CH.dbd.CH--CH.dbd.CH C.I-327 A-3 H H H CH.dbd.CH--CH.dbd.CH C.I-328
A-4 H H H CH.dbd.CH--CH.dbd.CH C.I-329 A-5 H H H
CH.dbd.CH--CH.dbd.CH C.I-330 A-6 H H H CH.dbd.CH--CH.dbd.CH C.I-331
A-7 H H H CH.dbd.CH--CH.dbd.CH C.I-332 A-8 H H H
CH.dbd.CH--CH.dbd.CH C.I-333 A-9 H H H CH.dbd.CH--CH.dbd.CH C.I-334
A-1 H Cl H CH.dbd.CH--CH.dbd.CH C.I-335 A-2 H Cl H
CH.dbd.CH--CH.dbd.CH C.I-336 A-3 H Cl H CH.dbd.CH--CH.dbd.CH
C.I-337 A-4 H Cl H CH.dbd.CH--CH.dbd.CH C.I-338 A-5 H Cl H
CH.dbd.CH--CH.dbd.CH C.I-339 A-6 H Cl H CH.dbd.CH--CH.dbd.CH
C.I-340 A-7 H Cl H CH.dbd.CH--CH.dbd.CH C.I-341 A-8 H Cl H
CH.dbd.CH--CH.dbd.CH C.I-342 A-9 H Cl H CH.dbd.CH--CH.dbd.CH
C.I-343 A-1 Cl H H CH.dbd.CH--CH.dbd.CH C.I-344 A-2 Cl H H
CH.dbd.CH--CH.dbd.CH C.I-345 A-3 Cl H H CH.dbd.CH--CH.dbd.CH
C.I-346 A-4 Cl H H CH.dbd.CH--CH.dbd.CH C.I-347 A-5 Cl H H
CH.dbd.CH--CH.dbd.CH C.I-348 A-6 Cl H H CH.dbd.CH--CH.dbd.CH
C.I-349 A-7 Cl H H CH.dbd.CH--CH.dbd.CH C.I-350 A-8 Cl H H
CH.dbd.CH--CH.dbd.CH C.I-351 A-9 Cl H H CH.dbd.CH--CH.dbd.CH
C.I-352 A-1 Cl Cl H CH.dbd.CH--CH.dbd.CH C.I-353 A-2 Cl Cl H
CH.dbd.CH--CH.dbd.CH C.I-354 A-3 Cl Cl H CH.dbd.CH--CH.dbd.CH
C.I-355 A-4 Cl Cl H CH.dbd.CH--CH.dbd.CH C.I-356 A-5 Cl Cl H
CH.dbd.CH--CH.dbd.CH C.I-357 A-6 Cl Cl H CH.dbd.CH--CH.dbd.CH
C.I-358 A-7 Cl Cl H CH.dbd.CH--CH.dbd.CH C.I-359 A-8 Cl Cl H
CH.dbd.CH--CH.dbd.CH C.I-360 A-9 Cl Cl H CH.dbd.CH--CH.dbd.CH
C.I-361 A-1 CF.sub.3 H H CH.dbd.CH--CH.dbd.CH C.I-362 A-2 CF.sub.3
H H CH.dbd.CH--CH.dbd.CH C.I-363 A-3 CF.sub.3 H H
CH.dbd.CH--CH.dbd.CH C.I-364 A-4 CF.sub.3 H H CH.dbd.CH--CH.dbd.CH
C.I-365 A-5 CF.sub.3 H H CH.dbd.CH--CH.dbd.CH C.I-366 A-6 CF.sub.3
H H CH.dbd.CH--CH.dbd.CH C.I-367 A-7 CF.sub.3 H H
CH.dbd.CH--CH.dbd.CH C.I-368 A-8 CF.sub.3 H H CH.dbd.CH--CH.dbd.CH
C.I-369 A-9 CF.sub.3 H H CH.dbd.CH--CH.dbd.CH C.I-370 A-1 CF.sub.3
Cl H CH.dbd.CH--CH.dbd.CH C.I-371 A-2 CF.sub.3 Cl H
CH.dbd.CH--CH.dbd.CH C.I-372 A-3 CF.sub.3 Cl H CH.dbd.CH--CH.dbd.CH
C.I-373 A-4 CF.sub.3 Cl H CH.dbd.CH--CH.dbd.CH C.I-374 A-5 CF.sub.3
Cl H CH.dbd.CH--CH.dbd.CH C.I-375 A-6 CF.sub.3 Cl H
CH.dbd.CH--CH.dbd.CH C.I-376 A-7 CF.sub.3 Cl H CH.dbd.CH--CH.dbd.CH
C.I-377 A-8 CF.sub.3 Cl H CH.dbd.CH--CH.dbd.CH C.I-378 A-9 CF.sub.3
Cl H CH.dbd.CH--CH.dbd.CH C.I-379 A-1 H H Cl CH.dbd.CH--CH.dbd.CH
C.I-380 A-2 H H Cl CH.dbd.CH--CH.dbd.CH C.I-381 A-3 H H Cl
CH.dbd.CH--CH.dbd.CH C.I-382 A-4 H H Cl CH.dbd.CH--CH.dbd.CH
C.I-383 A-5 H H Cl CH.dbd.CH--CH.dbd.CH C.I-384 A-6 H H Cl
CH.dbd.CH--CH.dbd.CH C.I-385 A-7 H H Cl CH.dbd.CH--CH.dbd.CH
C.I-386 A-8 H H Cl CH.dbd.CH--CH.dbd.CH C.I-387 A-9 H H Cl
CH.dbd.CH--CH.dbd.CH C.I-388 A-1 H Cl Cl CH.dbd.CH--CH.dbd.CH
C.I-389 A-2 H Cl Cl CH.dbd.CH--CH.dbd.CH C.I-390 A-3 H Cl Cl
CH.dbd.CH--CH.dbd.CH C.I-391 A-4 H Cl Cl CH.dbd.CH--CH.dbd.CH
C.I-392 A-5 H Cl Cl CH.dbd.CH--CH.dbd.CH C.I-393 A-6 H Cl Cl
CH.dbd.CH--CH.dbd.CH C.I-394 A-7 H Cl Cl CH.dbd.CH--CH.dbd.CH
C.I-395 A-8 H Cl Cl CH.dbd.CH--CH.dbd.CH C.I-396 A-9 H Cl Cl
CH.dbd.CH--CH.dbd.CH C.I-397 A-1 Cl H Cl CH.dbd.CH--CH.dbd.CH
C.I-398 A-2 Cl H Cl CH.dbd.CH--CH.dbd.CH C.I-399 A-3 Cl H Cl
CH.dbd.CH--CH.dbd.CH C.I-400 A-4 Cl H Cl CH.dbd.CH--CH.dbd.CH
C.I-401 A-5 Cl H Cl CH.dbd.CH--CH.dbd.CH C.I-402 A-6 Cl H Cl
CH.dbd.CH--CH.dbd.CH C.I-403 A-7 Cl H Cl CH.dbd.CH--CH.dbd.CH
C.I-404 A-8 Cl H Cl CH.dbd.CH--CH.dbd.CH C.I-405 A-9 Cl H Cl
CH.dbd.CH--CH.dbd.CH C.I-406 A-1 Cl Cl Cl CH.dbd.CH--CH.dbd.CH
C.I-407 A-2 Cl Cl Cl CH.dbd.CH--CH.dbd.CH C.I-408 A-3 Cl Cl Cl
CH.dbd.CH--CH.dbd.CH C.I-409 A-4 Cl Cl Cl CH.dbd.CH--CH.dbd.CH
C.I-410 A-5 Cl Cl Cl CH.dbd.CH--CH.dbd.CH C.I-411 A-6 Cl Cl Cl
CH.dbd.CH--CH.dbd.CH C.I-412 A-7 Cl Cl Cl CH.dbd.CH--CH.dbd.CH
C.I-413 A-8 Cl Cl Cl CH.dbd.CH--CH.dbd.CH C.I-414 A-9 Cl Cl Cl
CH.dbd.CH--CH.dbd.CH C.I-415 A-1 CF.sub.3 H Cl CH.dbd.CH--CH.dbd.CH
C.I-416 A-2 CF.sub.3 H Cl CH.dbd.CH--CH.dbd.CH C.I-417 A-3 CF.sub.3
H Cl CH.dbd.CH--CH.dbd.CH C.I-418 A-4 CF.sub.3 H Cl
CH.dbd.CH--CH.dbd.CH C.I-419 A-5 CF.sub.3 H Cl CH.dbd.CH--CH.dbd.CH
C.I-420 A-6 CF.sub.3 H Cl CH.dbd.CH--CH.dbd.CH C.I-421 A-7 CF.sub.3
H Cl CH.dbd.CH--CH.dbd.CH C.I-422 A-8 CF.sub.3 H Cl
CH.dbd.CH--CH.dbd.CH C.I-423 A-9 CF.sub.3 H Cl CH.dbd.CH--CH.dbd.CH
C.I-424 A-1 CF.sub.3 Cl Cl CH.dbd.CH--CH.dbd.CH C.I-425 A-2
CF.sub.3 Cl Cl CH.dbd.CH--CH.dbd.CH C.I-426 A-3 CF.sub.3 Cl Cl
CH.dbd.CH--CH.dbd.CH C.I-427 A-4 CF.sub.3 Cl Cl
CH.dbd.CH--CH.dbd.CH C.I-428 A-5 CF.sub.3 Cl Cl
CH.dbd.CH--CH.dbd.CH C.I-429 A-6 CF.sub.3 Cl Cl
CH.dbd.CH--CH.dbd.CH C.I-430 A-7 CF.sub.3 Cl Cl
CH.dbd.CH--CH.dbd.CH C.I-431 A-8 CF.sub.3 Cl Cl
CH.dbd.CH--CH.dbd.CH C.I-432 A-9 CF.sub.3 Cl Cl
CH.dbd.CH--CH.dbd.CH C.I-433 A-1 H H CF.sub.3 CH.dbd.CH--CH.dbd.CH
C.I-434 A-2 H H CF.sub.3 CH.dbd.CH--CH.dbd.CH C.I-435 A-3 H H
CF.sub.3 CH.dbd.CH--CH.dbd.CH C.I-436 A-4 H H CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-437 A-5 H H CF.sub.3 CH.dbd.CH--CH.dbd.CH
C.I-438 A-6 H H CF.sub.3 CH.dbd.CH--CH.dbd.CH C.I-439 A-7 H H
CF.sub.3 CH.dbd.CH--CH.dbd.CH C.I-440 A-8 H H CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-441 A-9 H H CF.sub.3 CH.dbd.CH--CH.dbd.CH
C.I-442 A-1 H Cl CF.sub.3 CH.dbd.CH--CH.dbd.CH C.I-443 A-2 H Cl
CF.sub.3 CH.dbd.CH--CH.dbd.CH C.I-444 A-3 H Cl CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-445 A-4 H Cl CF.sub.3 CH.dbd.CH--CH.dbd.CH
C.I-446 A-5 H Cl CF.sub.3 CH.dbd.CH--CH.dbd.CH C.I-447 A-6 H Cl
CF.sub.3 CH.dbd.CH--CH.dbd.CH C.I-448 A-7 H Cl CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-449 A-8 H Cl CF.sub.3 CH.dbd.CH--CH.dbd.CH
C.I-450 A-9 H Cl CF.sub.3 CH.dbd.CH--CH.dbd.CH C.I-451 A-1 Cl H
CF.sub.3 CH.dbd.CH--CH.dbd.CH C.I-452 A-2 Cl H CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-453 A-3 Cl H CF.sub.3 CH.dbd.CH--CH.dbd.CH
C.I-454 A-4 Cl H CF.sub.3 CH.dbd.CH--CH.dbd.CH C.I-455 A-5 Cl H
CF.sub.3 CH.dbd.CH--CH.dbd.CH C.I-456 A-6 Cl H CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-457 A-7 Cl H CF.sub.3 CH.dbd.CH--CH.dbd.CH
C.I-458 A-8 Cl H CF.sub.3 CH.dbd.CH--CH.dbd.CH C.I-459 A-9 Cl H
CF.sub.3 CH.dbd.CH--CH.dbd.CH C.I-460 A-1 Cl Cl CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-461 A-2 Cl Cl CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-462 A-3 Cl Cl CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-463 A-4 Cl Cl CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-464 A-5 Cl Cl CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-465 A-6 Cl Cl CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-466 A-7 Cl Cl CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-467 A-8 Cl Cl CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-468 A-9 Cl Cl CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-469 A-1 CF.sub.3 H CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-470 A-2 CF.sub.3 H CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-471 A-3 CF.sub.3 H CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-472 A-4 CF.sub.3 H CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-473 A-5 CF.sub.3 H CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-474 A-6 CF.sub.3 H CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-475 A-7 CF.sub.3 H CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-476 A-8 CF.sub.3 H CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-477 A-9 CF.sub.3 H CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-478 A-1 CF.sub.3 Cl CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-479 A-2 CF.sub.3 Cl CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-480 A-3 CF.sub.3 Cl CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-481 A-4 CF.sub.3 Cl CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-482 A-5 CF.sub.3 Cl CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-483 A-6 CF.sub.3 Cl CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-484 A-7 CF.sub.3 Cl CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-485 A-8 CF.sub.3 Cl CF.sub.3
CH.dbd.CH--CH.dbd.CH C.I-486 A-9 CF.sub.3 Cl CF.sub.3
CH.dbd.CH--CH.dbd.CH
[0108] The examples of compounds I of formula I of table C.I.1
include their tautomers, racemic mixtures, individual pure
enantiomers and diasteroemers and their optically active
mixtures.
General Preparation Methods of Compounds of Formula I
[0109] The active compounds I can be prepared according to methods
as described in WO2005/085216, WO2007/074789 or in
WO2007/079162.
Preferred Active Compounds II Selected from Group A
[0110] With respect to their use in the pesticidal mixtures of the
present invention, particular preference is given to the compounds
C.II as listed in the paragraphs below.
[0111] With regard to the use in a pesticidal mixture of the
present invention, the compound II selected from group A.1 as
defined above is preferably triazemate or primicarb.
[0112] With regard to the use in a pesticidal mixture of the
present invention, the compound II selected from group A.2 as
defined above is preferably endosulfan,
N-Ethyl-2,2-dimethylpropionamide-2-(2,6-dichloro-.alpha...alpha...alpha.--
trifluoro-p-tolyl) hydrazon,
N-Ethyl-2,2-dichloro-1-methylcyclopropane-carboxamide-2-(2,6-dichloro-.al-
pha...alpha...alpha.-trifluoro-p-tolyl) hydrazon, acetoprole,
ethiprole, fipronil, pyrafluprole, pyriprole or vaniliprole or the
phenylpyrazole compound II.A.sup.2.1.
[0113] More preferably the compound II is
N-Ethyl-2,2-dimethylpropionamide-2-(2,6-dichloro-.alpha...alpha...alpha.--
trifluoro-p-tolyl) hydrazon,
N-Ethyl-2,2-dichloro-1-methylcyclopropane-carboxamide-2-(2,6-dichloro-.al-
pha...alpha...alpha.-trifluoro-p-tolyl) hydrazon, acetoprole or
fipronil.
[0114] With regard to the use in a pesticidal mixture of the
present invention, the compound II selected from group A.3 as
defined above is preferably allethrin, bifenthrin, cyfluthrin,
lambda-cyhalothrin, cypermethrin, alpha-cypermethrin,
beta-cypermethrin, zeta-cypermethrin, deltamethrin, etofenprox,
fenpropathrin, fenvalerate, flucythrinate, tau-fluvalinate,
silafluofen or tralomethrin.
[0115] More preferably the compound II is alpha-cypermethrin or
deltamethrin.
[0116] With regard to the use in a pesticidal mixture of the
present invention, the compound II selected from group A.4 as
defined above is preferably thiocyclam or from the class of
neonicotinoids acteamiprid, chlothianidin, dinotefuran,
imidacloprid, nitenpyram, thiacloprid, thiamethoxam and AKD-1022;
or the allosteric nicotinic acteylcholine receptor agonist
spinosad.
[0117] More preferably the compound II is clothianidine,
imidacloprid or thiamethoxam.
[0118] With regard to the use in a pesticidal mixture of the
present invention, the compound II selected from group A.5 as
defined above is preferably abamectin, emamectin benzoate,
lepimectin or milbemectin.
[0119] More preferably the compound II is abamectin.
[0120] With regard to the use in a pesticidal mixture of the
present invention, the compound II selected from group A.7 as
defined above is preferably diafenthiuron.
[0121] With regard to the use in a pesticidal mixture of the
present invention, the compound II selected from group A.8 as
defined above is preferably buprofezin.
[0122] With regard to the use in a pesticidal mixture of the
present invention, the compound II selected from group A.10 as
defined above is preferably pyridaben or flufenerim.
[0123] With regard to the use in a pesticidal mixture of the
present invention, the compound II selected from group A.11 as
defined above is preferably indoxacarb or metaflumizone. More
preferably the compound II is metaflumizone.
[0124] With regard to the use in a pesticidal mixture of the
present invention, the compound II selected from group A.12 as
defined above is preferably spirodiclofen, spiromesifen or
spirotetramat.
[0125] More preferably the compound II is spiromesifen or
spirotetramat.
[0126] With regard to the use in a pesticidal mixture of the
present invention, the compound II selected from group A.13 as
defined above is preferably amitraz, flonicamid, flubendiamine,
pymetrozine, pyridalyl, pyrifluquinazon, chlorantraniliproler, the
anthranil compound II.A.sup.13.1 or the sulfoximine compounds
II.A.sup.13.2, II.A.sup.13.3 or II.A.sup.13.4.
[0127] More preferably the compound II is flonicamid, pymetrozine,
pyrifluquinazon, chlorantraniliprole or the anthranil compound
II.A.sup.13.1.
[0128] Especially preferred are pesticidal mixtures containing
N-Ethyl-2,2-dimethylpropionamide-2-(2,6-dichloro-.alpha...alpha...alpha.--
trifluoro-p-tolyl) hydrazon as compound II.
[0129] Especially preferred are pesticidal mixtures containing
N-Ethyl-2,2-dichloro-1-methylcyclopropane-carboxamide-2-(2,6-dichloro-.al-
pha...alpha...alpha.-trifluoro-p-tolyl) hydrazon as compound
II.
[0130] Especially preferred are pesticidal mixtures containing
acetoprole as compound II.
[0131] Especially preferred are pesticidal mixtures containing
fipronil as compound II.
[0132] Especially preferred are pesticidal mixtures containing
alpha-cypermethrin as compound II.
[0133] Especially preferred are pesticidal mixtures containing
clothianidin as compound II.
[0134] Especially preferred are pesticidal mixtures containing
imidacloprid as compound II.
[0135] Especially preferred are pesticidal mixtures containing
thiamethoxam as compound II.
[0136] Especially preferred are pesticidal mixtures containing
pymetrozine as compound II.
[0137] Especially preferred are pesticidal mixtures containing
flonicamid as compound II.
[0138] Especially preferred are pesticidal mixtures containing
spiromesifen as compound II.
[0139] Especially preferred are pesticidal mixtures containing
spirotetramat as compound II.
[0140] Especially preferred are pesticidal mixtures containing
pyrifluquinazon as compound II.
[0141] Especially preferred are pesticidal mixtures containing
chlorantraniliprole as compound II.
[0142] Especially preferred are pesticidal mixtures containing the
anthranilamid compound II.A.sup.13.1
##STR00008##
as compound II.
[0143] Especially preferred are pesticidal mixtures containing the
sulfoximine compound
##STR00009##
as compound II.
[0144] Especially preferred are pesticidal mixtures containing the
sulfoximine compound II.A.sup.13.3
##STR00010##
as compound II.
[0145] Especially preferred are pesticidal mixtures containing the
sulfoximine compound II.A.sup.13.4
##STR00011##
as compound II.
Preferred Mixtures According to the Invention
[0146] Especially preferred are inventive mixtures wherein the
compound II of group A is acetoprol and the compound I of formula I
is a compound of Table C.I.1.
[0147] Especially preferred are inventive mixtures wherein the
compound II of group A is fipronil and the compound I of formula I
is a compound of Table C.I.1.
[0148] Especially preferred are inventive mixtures wherein the
compound II of group A is
N-Ethyl-2,2-dimethylpropionamide-2-(2,6-dichloro-.alpha...alpha...alpha.--
trifluoro-p-tolyl) hydrazon and the compound I of formula I is a
compound of Table C.I.1.
[0149] Especially preferred are inventive mixtures wherein the
compound II of group A is
N-Ethyl-2,2-dichloro-1-methylcyclopropane-carboxamide-2-(2,6-dichloro-.al-
pha...alpha...alpha.-trifluoro-p-tolyl) hydrazon and the compound I
of formula I is a compound of Table C.I.1.
[0150] Especially preferred are inventive mixtures wherein the
compound II of group A is alpha-cypermethrin and the compound I of
formula I is a compound of Table C.I.1.
[0151] Especially preferred are inventive mixtures wherein the
compound II of group A is deltamethrin and the compound I of
formula I is a compound of Table C.I.1.
[0152] Especially preferred are inventive mixtures wherein the
compound II of group A is clothianidin and the compound I of
formula I is a compound of Table C.I.1.
[0153] Especially preferred are inventive mixtures wherein the
compound II of group A is imidacloprid and the compound I of
formula I is a compound of Table C.I.1.
[0154] Especially preferred are inventive mixtures wherein the
compound II of group A is thiamethoxam and the compound I of
formula I is a compound of Table C.I.1.
[0155] Especially preferred are inventive mixtures wherein the
compound II of group A is abamectin and the compound I of formula I
is a compound of Table C.I.1.
[0156] Especially preferred are inventive mixtures wherein the
compound II of group A is pymetrozine and the compound I of formula
I is a compound of Table C.I.1.
[0157] Especially preferred are inventive mixtures wherein the
compound II of group A is flonicamid and the compound I of formula
I is a compound of Table C.I.1.
[0158] Especially preferred are inventive mixtures wherein the
compound II of group A is diafenthiuron and the compound I of
formula I is a compound of Table C.I.1.
[0159] Especially preferred are inventive mixtures wherein the
compound II of group A is buprofezin and the compound I of formula
I is a compound of Table C.I.1.
[0160] Especially preferred are inventive mixtures wherein the
compound II of group A is pyridaben and the compound I of formula I
is a compound of Table C.I.1.
[0161] Especially preferred are inventive mixtures wherein the
compound II of group A is flufenerim and the compound I of formula
I is a compound of Table C.I.1.
[0162] Especially preferred are inventive mixtures wherein the
compound II of group A is metaflumizone and the compound I of
formula I is a compound of Table C.I.1.
[0163] Especially preferred are inventive mixtures wherein the
compound II of group A is spiromesifen and the compound I of
formula I is a compound of Table C.I.1.
[0164] Especially preferred are inventive mixtures wherein the
compound II of group A is spirotetramat and the compound I of
formula I is a compound of Table C.I.1.
[0165] Especially preferred are inventive mixtures wherein the
compound II of group A is pyrifluquinazon and the compound I of
formula I is a compound of Table C.I.1.
[0166] Especially preferred are inventive mixtures wherein the
compound II of group A is chlorantraniliprole and the compound I of
formula I is a compound of Table C.I.1.
[0167] Especially preferred are inventive mixtures wherein the
compound II of group A is the anthranilamid compound II.A.sup.13.1
and the compound I of formula I is a compound of Table C.I.1.
[0168] Especially preferred are inventive mixtures wherein the
compound II of group A is the sulfoximine compound II.A.sup.13.2
and the compound I of formula I is a compound of Table C.I.1.
[0169] Especially preferred are inventive mixtures wherein the
compound II of group A is the sulfoximine compound II.A.sup.13.3
and the compound I of formula I is a compound of Table C.I.1.
[0170] Especially preferred are inventive mixtures wherein the
compound II of group A is the sulfoximine compound II.A.sup.13.4
and the compound I of formula I is a compound of Table C.I.1.
[0171] The following table M represents preferred combinations of
the active compounds I of formula I as defined in table C.I.1 and
the active compounds II of group A in mixtures according to the
invention:
TABLE-US-00002 TABLE M Mixture Compound I Compound-II Mixture
Compound I Compound II M.1 C.I-37 acetoprole M.221 C.I-37
diafenthiuron M.2 C.I-40 acetoprole M.222 C.I-40 diafenthiuron M.3
C.I-73 acetoprole M.223 C.I-73 diafenthiuron M.4 C.I-76 acetoprole
M.224 C.I-76 diafenthiuron M.5 C.I-145 acetoprole M.225 C.I-145
diafenthiuron M.6 C.I-148 acetoprole M.226 C.I-148 diafenthiuron
M.7 C.I-199 acetoprole M.227 C.I-199 diafenthiuron M.8 C.I-202
acetoprole M.228 C.I-202 diafenthiuron M.9 C.I-235 acetoprole M.229
C.I-235 diafenthiuron M.10 C.I-238 acetoprole M.230 C.I-238
diafenthiuron M.11 C.I.240 acetoprole M.231 C.I.240 diafenthiuron
M.12 C.I-244 acetoprole M.232 C.I-244 diafenthiuron M.13 C.I-247
acetoprole M.233 C.I-247 diafenthiuron M.14 C.I-307 acetoprole
M.234 C.I-307 diafenthiuron M.15 C.I-310 acetoprole M.235 C.I-310
diafenthiuron M.16 C.I-361 acetoprole M.236 C.I-361 diafenthiuron
M.17 C.I-364 acetoprole M.237 C.I-364 diafenthiuron M.18 C.I-397
acetoprole M.238 C.I-397 diafenthiuron M.19 C.I-400 acetoprole
M.239 C.I-400 diafenthiuron M.20 C.I-406 acetoprole M.240 C.I-406
diafenthiuron M.21 C.I-409 acetoprole M.241 C.I-409 diafenthiuron
M.22 C.I-469 acetoprole M.242 C.I-469 diafenthiuron M.23 C.I-472
acetoprole M.243 C.I-472 diafenthiuron M.24 C.I-37 fipronil M.244
C.I-37 buprofezin M.25 C.I-40 fipronil M.245 C.I-40 buprofezin M.26
C.I-73 fipronil M.246 C.I-73 buprofezin M.27 C.I-76 fipronil M.247
C.I-76 buprofezin M.28 C.I-145 fipronil M.248 C.I-145 buprofezin
M.29 C.I-148 fipronil M.249 C.I-148 buprofezin M.30 C.I-199
fipronil M.250 C.I-199 buprofezin M.31 C.I-202 fipronil M.251
C.I-202 buprofezin M.32 C.I-235 fipronil M.252 C.I-235 buprofezin
M.33 C.I-238 fipronil M.253 C.I-238 buprofezin M.34 C.I.240
fipronil M.254 C.I.240 buprofezin M.35 C.I-244 fipronil M.255
C.I-244 buprofezin M.36 C.I-247 fipronil M.256 C.I-247 buprofezin
M.37 C.I-307 fipronil M.257 C.I-307 buprofezin M.38 C.I-310
fipronil M.258 C.I-310 buprofezin M.39 C.I-361 fipronil M.259
C.I-361 buprofezin M.40 C.I-364 fipronil M.260 C.I-364 buprofezin
M.41 C.I-397 fipronil M.261 C.I-397 buprofezin M.42 C.I-400
fipronil M.262 C.I-400 buprofezin M.43 C.I-406 fipronil M.263
C.I-406 buprofezin M.44 C.I-409 fipronil M.264 C.I-409 buprofezin
M.45 C.I-469 fipronil M.265 C.I-469 buprofezin M.46 C.I-472
fipronil M.266 C.I-472 buprofezin M.47 C.I-37 imidacloprid M.267
C.I-37 pyridaben M.48 C.I-40 imidacloprid M.268 C.I-40 pyridaben
M.49 C.I-73 imidacloprid M.269 C.I-73 pyridaben M.50 C.I-76
imidacloprid M.270 C.I-76 pyridaben M.51 C.I-145 imidacloprid M.271
C.I-145 pyridaben M.52 C.I-148 imidacloprid M.272 C.I-148 pyridaben
M.53 C.I-199 imidacloprid M.273 C.I-199 pyridaben M.54 C.I-202
imidacloprid M.274 C.I-202 pyridaben M.55 C.I-235 imidacloprid
M.275 C.I-235 pyridaben M.56 C.I-238 imidacloprid M.276 C.I-238
pyridaben M.57 C.I.240 imidacloprid M.277 C.I.240 pyridaben M.58
C.I-244 imidacloprid M.278 C.I-244 pyridaben M.59 C.I-247
imidacloprid M.279 C.I-247 pyridaben M.60 C.I-307 imidacloprid
M.280 C.I-307 pyridaben M.61 C.I-310 imidacloprid M.281 C.I-310
pyridaben M.62 C.I-361 imidacloprid M.282 C.I-361 pyridaben M.63
C.I-364 imidacloprid M.283 C.I-364 pyridaben M.64 C.I-397
imidacloprid M.284 C.I-397 pyridaben M.65 C.I-400 imidacloprid
M.285 C.I-400 pyridaben M.66 C.I-406 imidacloprid M.286 C.I-406
pyridaben M.67 C.I-409 imidacloprid M.287 C.I-409 pyridaben M.68
C.I-469 imidacloprid M.288 C.I-469 pyridaben M.69 C.I-472
imidacloprid M.289 C.I-472 pyridaben M.70 C.I-37 abamectin M.290
C.I-37 spiromesifen M.71 C.I-40 abamectin M.291 C.I-40 spiromesifen
M.72 C.I-73 abamectin M.292 C.I-73 spiromesifen M.73 C.I-76
abamectin M.293 C.I-76 spiromesifen M.74 C.I-145 abamectin M.294
C.I-145 spiromesifen M.75 C.I-148 abamectin M.295 C.I-148
spiromesifen M.76 C.I-199 abamectin M.296 C.I-199 spiromesifen M.77
C.I-202 abamectin M.297 C.I-202 spiromesifen M.78 C.I-235 abamectin
M.298 C.I-235 spiromesifen M.79 C.I-238 abamectin M.299 C.I-238
spiromesifen M.80 C.I.240 abamectin M.300 C.I.240 spiromesifen M.81
C.I-244 abamectin M.301 C.I-244 spiromesifen M.82 C.I-247 abamectin
M.302 C.I-247 spiromesifen M.83 C.I-307 abamectin M.303 C.I-307
spiromesifen M.84 C.I-310 abamectin M.304 C.I-310 spiromesifen M.85
C.I-361 abamectin M.305 C.I-361 spiromesifen M.86 C.I-364 abamectin
M.306 C.I-364 spiromesifen M.87 C.I-397 abamectin M.307 C.I-397
spiromesifen M.88 C.I-400 abamectin M.308 C.I-400 spiromesifen M.89
C.I-406 abamectin M.309 C.I-406 spiromesifen M.90 C.I-409 abamectin
M.310 C.I-409 spiromesifen M.91 C.I-469 abamectin M.311 C.I-469
spiromesifen M.92 C.I-472 abamectin M.312 C.I-472 spiromesifen M.93
C.I-37 anthranilamid M.313 C.I-37 chlorantraniliprole II.A.sup.13.1
M.94 C.I-40 anthranilamid M.314 C.I-40 chlorantraniliprole
II.A.sup.13.1 M.95 C.I-73 anthranilamid M.315 C.I-73
chlorantraniliprole II.A.sup.13.1 M.96 C.I-76 anthranilamid M.316
C.I-76 chlorantraniliprole II.A.sup.13.1 M.97 C.I-145 anthranilamid
M.317 C.I-145 chlorantraniliprole II.A.sup.13.1 M.98 C.I-148
anthranilamid M.318 C.I-148 chlorantraniliprole II.A.sup.13.1 M.99
C.I-199 anthranilamid M.319 C.I-199 chlorantraniliprole
II.A.sup.13.1 M.100 C.I-202 anthranilamid M.320 C.I-202
chlorantraniliprole II.A.sup.13.1 M.101 C.I-235 anthranilamid M.321
C.I-235 chlorantraniliprole II.A.sup.13.1 M.102 C.I-238
anthranilamid M.322 C.I-238 chlorantraniliprole II.A.sup.13.1 M.103
C.I.240 anthranilamid M.323 C.I.240 chlorantraniliprole
II.A.sup.13.1 M.104 C.I-244 anthranilamid M.324 C.I-244
chlorantraniliprole II.A.sup.13.1 M.105 C.I-247 anthranilamid M.325
C.I-247 chlorantraniliprole II.A.sup.13.1 M.106 C.I-307
anthranilamid M.326 C.I-307 chlorantraniliprole II.A.sup.13.1 M.107
C.I-310 anthranilamid M.327 C.I-310 chlorantraniliprole
II.A.sup.13.1 M.108 C.I-361 anthranilamid M.328 C.I-361
chlorantraniliprole II.A.sup.13.1 M.109 C.I-364 anthranilamid M.329
C.I-364 chlorantraniliprole II.A.sup.13.1 M.110 C.I-397
anthranilamid M.330 C.I-397 chlorantraniliprole II.A.sup.13.1 M.111
C.I-400 anthranilamid M.331 C.I-400 chlorantraniliprole
II.A.sup.13.1 M.112 C.I-406 anthranilamid M.332 C.I-406
chlorantraniliprole II.A.sup.13.1 M.113 C.I-409 anthranilamid M.333
C.I-409 chlorantraniliprole II.A.sup.13.1 M.114 C.I-469
anthranilamid M.334 C.I-469 chlorantraniliprole II.A.sup.13.1 M.115
C.I-472 anthranilamid M.335 C.I-472 chlorantraniliprole
II.A.sup.13.1 M.116 C.I-37 deltamethrin M.336 C.I-37 flufenerim
M.117 C.I-40 deltamethrin M.337 C.I-40 flufenerim M.118 C.I-73
deltamethrin M.338 C.I-73 flufenerim M.119 C.I-76 deltamethrin
M.339 C.I-76 flufenerim M.120 C.I-145 deltamethrin M.340 C.I-145
flufenerim M.121 C.I-148 deltamethrin M.341 C.I-148 flufenerim
M.122 C.I-199 deltamethrin M.342 C.I-199 flufenerim M.123 C.I-202
deltamethrin M.343 C.I-202 flufenerim M.124 C.I-235 deltamethrin
M.344 C.I-235 flufenerim M.125 C.I-238 deltamethrin M.345 C.I-238
flufenerim M.126 C.I.240 deltamethrin M.346 C.I.240 flufenerim
M.127 C.I-244 deltamethrin M.347 C.I-244 flufenerim M.128 C.I-247
deltamethrin M.348 C.I-247 flufenerim M.129 C.I-307 deltamethrin
M.349 C.I-307 flufenerim M.130 C.I-310 deltamethrin M.350 C.I-310
flufenerim M.131 C.I-361 deltamethrin M.351 C.I-361 flufenerim
M.132 C.I-364 deltamethrin M.352 C.I-364 flufenerim M.133 C.I-397
deltamethrin M.353 C.I-397 flufenerim M.134 C.I-400 deltamethrin
M.354 C.I-400 flufenerim M.135 C.I-406 deltamethrin M.355 C.I-406
flufenerim M.136 C.I-409 deltamethrin M.356 C.I-409 flufenerim
M.137 C.I-469 deltamethrin M.357 C.I-469 flufenerim M.138 C.I-472
deltamethrin M.358 C.I-472 flufenerim M.139 C.I-37 metaflumizone
M.359 C.I-37 .alpha.-cypermethrin M.140 C.I-40 metaflumizone M.360
C.I-40 .alpha.-cypermethrin M.141 C.I-73 metaflumizone M.361 C.I-73
.alpha.-cypermethrin M.142 C.I-76 metaflumizone M.362 C.I-76
.alpha.-cypermethrin M.143 C.I-145 metaflumizone M.363 C.I-145
.alpha.-cypermethrin M.144 C.I-148 metaflumizone M.364 C.I-148
.alpha.-cypermethrin M.145 C.I-199 metaflumizone M.365 C.I-199
.alpha.-cypermethrin M.146 C.I-202 metaflumizone M.366 C.I-202
.alpha.-cypermethrin M.147 C.I-235 metaflumizone M.367 C.I-235
.alpha.-cypermethrin M.148 C.I-238 metaflumizone M.368 C.I-238
.alpha.-cypermethrin M.149 C.I.240 metaflumizone M.369 C.I.240
.alpha.-cypermethrin M.150 C.I-244 metaflumizone M.370 C.I-244
.alpha.-cypermethrin M.151 C.I-247 metaflumizone M.371 C.I-247
.alpha.-cypermethrin M.152 C.I-307 metaflumizone M.372 C.I-307
.alpha.-cypermethrin M.153 C.I-310 metaflumizone M.373 C.I-310
.alpha.-cypermethrin M.154 C.I-361 metaflumizone M.374 C.I-361
.alpha.-cypermethrin M.155 C.I-364 metaflumizone M.375 C.I-364
.alpha.-cypermethrin M.156 C.I-397 metaflumizone M.376 C.I-397
.alpha.-cypermethrin M.157 C.I-400 metaflumizone M.377 C.I-400
.alpha.-cypermethrin M.158 C.I-406 metaflumizone M.378 C.I-406
.alpha.-cypermethrin M.159 C.I-409 metaflumizone M.379 C.I-409
.alpha.-cypermethrin M.160 C.I-469 metaflumizone M.380 C.I-469
.alpha.-cypermethrin M.161 C.I-472 metaflumizone M.381 C.I-472
.alpha.-cypermethrin M.162 C.I-37 clothianidine M.382 C.I-37
thiamethoxam M.163 C.I-40 clothianidine M.383 C.I-40 thiamethoxam
M.164 C.I-73 clothianidine M.384 C.I-73 thiamethoxam M.165 C.I-76
clothianidine M.385 C.I-76 thiamethoxam M.166 C.I-145 clothianidine
M.386 C.I-145 thiamethoxam M.167 C.I-148 clothianidine M.387
C.I-148 thiamethoxam M.168 C.I-199 clothianidine M.388 C.I-199
thiamethoxam M.169 C.I-202 clothianidine M.389 C.I-202 thiamethoxam
M.170 C.I-235 clothianidine M.390 C.I-235 thiamethoxam M.171
C.I-238 clothianidine M.391 C.I-238 thiamethoxam M.172 C.I.240
clothianidine M.392 C.I.240 thiamethoxam M.173 C.I-244
clothianidine M.393 C.I-244 thiamethoxam M.174 C.I-247
clothianidine M.394 C.I-247 thiamethoxam M.175 C.I-307
clothianidine M.395 C.I-307 thiamethoxam M.176 C.I-310
clothianidine M.396 C.I-310 thiamethoxam M.177 C.I-361
clothianidine M.397 C.I-361 thiamethoxam M.178 C.I-364
clothianidine M.398 C.I-364 thiamethoxam M.179 C.I-397
clothianidine M.399 C.I-397 thiamethoxam M.180 C.I-400
clothianidine M.400 C.I-400 thiamethoxam M.181 C.I-406
clothianidine M.401 C.I-406 thiamethoxam M.182 C.I-409
clothianidine M.402 C.I-409 thiamethoxam M.183 C.I-469
clothianidine M.403 C.I-469 thiamethoxam M.184 C.I-472
clothianidine M.404 C.I-472 thiamethoxam M.185 C.I-37 flonicamid
M.405 C.I-37 spirotetramat M.186 C.I-40 flonicamid M.406 C.I-40
spirotetramat M.187 C.I-73 flonicamid M.407 C.I-73 spirotetramat
M.188 C.I-76 flonicamid M.408 C.I-76 spirotetramat M.189 C.I-145
flonicamid M.409 C.I-145 spirotetramat M.190 C.I-148 flonicamid
M.410 C.I-148 spirotetramat M.191 C.I-199 flonicamid M.411 C.I-199
spirotetramat M.192 C.I-202 flonicamid M.412 C.I-202 spirotetramat
M.193 C.I-235 flonicamid M.413 C.I-235 spirotetramat M.194 C.I-238
flonicamid M.414 C.I-238 spirotetramat M.195 C.I.240 flonicamid
M.415 C.I.240 spirotetramat M.196 C.I-244 flonicamid M.416 C.I-244
spirotetramat M.197 C.I-247 flonicamid M.417 C.I-247 spirotetramat
M.198 C.I-307 flonicamid M.418 C.I-307 spirotetramat M.199 C.I-310
flonicamid M.419 C.I-310 spirotetramat M.200 C.I-361 flonicamid
M.420 C.I-361 spirotetramat M.201 C.I-364 flonicamid M.421 C.I-364
spirotetramat M.202 C.I-397 flonicamid M.422 C.I-397 spirotetramat
M.203 C.I-400 flonicamid M.423 C.I-400 spirotetramat M.204 C.I-406
flonicamid M.424 C.I-406 spirotetramat M.205 C.I-409 flonicamid
M.425 C.I-409 spirotetramat M.206 C.I-469 flonicamid M.426 C.I-469
spirotetramat M.207 C.I-472 flonicamid M.427 C.I-472 spirotetramat
M.208 C.I-37 pymetrozine M.428 C.I-37 pyrifluquinazone M.209 C.I-40
pymetrozine M.429 C.I-40 pyrifluquinazone M.210 C.I-73 pymetrozine
M.430 C.I-73 pyrifluquinazone M.211 C.I-76 pymetrozine M.431 C.I-76
pyrifluquinazone M.212 C.I-145 pymetrozine M.432 C.I-145
pyrifluquinazone M.213 C.I-148 pymetrozine M.433 C.I-148
pyrifluquinazone M.214 C.I-199 pymetrozine M.434 C.I-199
pyrifluquinazone M.215 C.I-202 pymetrozine M.435 C.I-202
pyrifluquinazone M.216 C.I-235 pymetrozine M.436 C.I-235
pyrifluquinazone M.217 C.I-238 pymetrozine M.437 C.I-238
pyrifluquinazone M.218 C.I.240 pymetrozine M.438 C.I.240
pyrifluquinazone M.219 C.I-244 pymetrozine M.439 C.I-244
pyrifluquinazone M.220 C.I-247 pymetrozine M.440 C.I-247
pyrifluquinazone M.221 C.I-307 pymetrozine M.441 C.I-307
pyrifluquinazone M.222 C.I-310 pymetrozine M.442 C.I-310
pyrifluquinazone M.223 C.I-361 pymetrozine M.443 C.I-361
pyrifluquinazone
M.224 C.I-364 pymetrozine M.444 C.I-364 pyrifluquinazone M.225
C.I-397 pymetrozine M.445 C.I-397 pyrifluquinazone M.226 C.I-400
pymetrozine M.446 C.I-400 pyrifluquinazone M.227 C.I-406
pymetrozine M.447 C.I-406 pyrifluquinazone M.228 C.I-409
pymetrozine M.448 C.I-409 pyrifluquinazone M.229 C.I-469
pymetrozine M.449 C.I-469 pyrifluquinazone M.230 C.I-472
pymetrozine M.450 C.I-472 pyrifluquinazone
Pests
[0172] The mixtures of the active compounds I and II, or the active
compounds I and II used simultaneously, that is jointly or
separately, exhibit outstanding action against pests from the
following orders:
[0173] Insects from the order of the lepidopterans (Lepidoptera),
for example Agrotis ypsilon, Agrotis segetum, Alabama argillacea,
Anticarsia gemmatalis, Argyresthia conjugella, Autographa gamma,
Bupalus piniarius, Cacoecia murinana, Capua reticulana, Cheimatobia
brumata, Choristoneura fumiferana, Choristoneura occidentalis,
Cirphis unipuncta, Cydia pomonella, Dendrolimus pini, Diaphania
nitidalis, Diatraea grandiosella, Earias insulana, Elasmopalpus
lignosellus, Eupoecilia ambiguella, Evetria bouliana, Feltia
subterranea, Galleria mellonella, Grapholitha funebrana,
Grapholitha molesta, Heliothis armigera, Heliothis virescens,
Heliothis zea, Hellula undalis, Hibernia defoliaria, Hyphantria
cunea, Hyponomeuta malinellus, Keiferia lycopersicella, Lambdina
fiscellaria, Laphygma exigua, Leucoptera coffeella, Leucoptera
scitella, Lithocolletis blancardella, Lobesia botrana, Loxostege
sticticalis, Lymantria dispar, Lymantria monacha, Lyonetia
clerkella, Malacosoma neustria, Mamestra brassicae, Orgyia
pseudotsugata, Ostrinia nubilalis, Panolis flammea, Pectinophora
gossypiella, Peridroma saucia, Phalera bucephala, Phthorimaea
operculella, Phyllocnistis citrella, Pieris brassicae, Plathypena
scabra, Plutella xylostella, Pseudoplusia includens, Rhyacionia
frustrana, Scrobipalpula absoluta, Sitotroga cerealella,
Sparganothis pilleriana, Spodoptera frugiperda, Spodoptera
littoralis, Spodoptera litura, Thaumatopoea pityocampa, Tortrix
viridana, Trichoplusia ni and Zeiraphera canadensis,
beetles (Coleoptera), for example Agrilus sinuatus, Agriotes
lineatus, Agriotes obscurus, Amphimallus solstitialis, Anisandrus
dispar, Anthonomus grandis, Anthonomus pomorum, Aphthona
euphoridae, Athous haemorrhoidalis, Atomaria linearis, Blastophagus
piniperda, Blitophaga undata, Bruchus rufimanus, Bruchus pisorum,
Bruchus lentis, Byctiscus betulae, Cassida nebulosa, Cerotoma
trifurcata, Cetonia aurata, Ceuthorrhynchus assimilis,
Ceuthorrhynchus napi, Chaetocnema tibialis, Conoderus vespertinus,
Crioceris asparagi, Ctenicera ssp., Diabrotica longicornis,
Diabrotica semipunctata, Diabrotica 12-punctata Diabrotica
speciosa, Diabrotica virgifera, Epilachna varivestis, Epitrix
hirtipennis, Eutinobothrus brasiliensis, Hylobius abietis, Hypera
brunneipennis, Hypera postica, Ips typographus, Lema bilineata,
Lema melanopus, Leptinotarsa decemlineata, Limonius californicus,
Lissorhoptrus oryzophilus, Melanotus communis, Meligethes aeneus,
Melolontha hippocastani, Melolontha melolontha, Oulema oryzae,
Ortiorrhynchus sulcatus, Otiorrhynchus ovatus, Phaedon cochleariae,
Phyllobius pyri, Phyllotreta chrysocephala, Phyllophaga sp.,
Phyllopertha horticola, Phyllotreta nemorum, Phyllotreta striolata,
Popillia japonica, Sitona lineatus and Sitophilus granaria, flies,
mosquitoes (Diptera), e.g. Aedes aegypti, Aedes albopictus, Aedes
vexans, Anastrepha ludens, Anopheles maculipennis, Anopheles
crucians, Anopheles albimanus, Anopheles gambiae, Anopheles
freeborni, Anopheles leucosphyrus, Anopheles minimus, Anopheles
quadrimaculatus, Calliphora vicina, Ceratitis capitata, Chrysomya
bezziana, Chrysomya hominivorax, Chrysomya macellaria, Chrysops
discalis, Chrysops silacea, Chrysops atlanticus, Cochliomyia
hominivorax, Contarinia sorghicola Cordylobia anthropophaga,
Culicoides furens, Culex pipiens, Culex nigripalpus, Culex
quinquefasciatus, Culex tarsalis, Culiseta inornata, Culiseta
melanura, Dacus cucurbitae, Dacus oleae, Dasineura brassicae, Delia
antique, Delia coarctata, Delia platura, Delia radicum, Dermatobia
hominis, Fannia canicularis, Geomyza Tripunctata, Gasterophilus
intestinalis, Glossina morsitans, Glossina palpalis, Glossina
fuscipes, Glossina tachinoides, Haematobia irritans, Haplodiplosis
equestris, Hippelates spp., Hylemyia platura, Hypoderma lineata,
Leptoconops torrens, Liriomyza sativae, Liriomyza trifolii, Lucilia
caprina, Lucilia cuprina, Lucilia sericata, Lycoria pectoralis,
Mansonia titillanus, Mayetiola destructor, Musca domestica, Muscina
stabulans, Oestrus ovis, Opomyza forum, Oscinella frit, Pegomya
hysocyami, Phorbia antiqua, Phorbia brassicae, Phorbia coarctata,
Phlebotomus argentipes, Psorophora columbiae, Psila rosae,
Psorophora discolor, Prosimulium mixtum, Rhagoletis cerasi,
Rhagoletis pomonella, Sarcophaga haemorrhoidalis, Sarcophaga sp.,
Simulium vittatum, Stomoxys calcitrans, Tabanus bovinus, Tabanus
atratus, Tabanus lineola, and Tabanus similis, Tipula oleracea, and
Tipula paludosa thrips (Thysanoptera), e.g. Dichromothrips
corbetti, Dichromothrips ssp, Frankliniella fusca, Frankliniella
occidentalis, Frankliniella tritici, Scirtothrips citri, Thrips
oryzae, Thrips palmi and Thrips tabaci, termites (Isoptera), e.g.
Calotermes flavicollis, Leucotermes flavipes, Heterotermes aureus,
Reticulitermes flavipes, Reticulitermes virginicus, Reticulitermes
lucifugus, Termes natalensis, and Coptotermes formosanus,
cockroaches (Blattaria-Blattodea), e.g. Blattella germanica,
Blattella asahinae, Periplaneta americana, Periplaneta japonica,
Periplaneta brunnea, Periplaneta fuligginosa, Periplaneta
australasiae, and Blatta orientalis, true bugs (Hemiptera), e.g.
Acrosternum hilare, Blissus leucopterus, Cyrtopeltis notatus,
Dysdercus cingulatus, Dysdercus intermedius, Eurygaster
integriceps, Euschistus impictiventris, Leptoglossus phyllopus,
Lygus lineolaris, Lygus pratensis, Nezara viridula, Piesma
quadrata, Solubea insularis, Thyanta perditor, Acyrthosiphon
onobrychis, Adelges laricis, Aphidula nasturtii, Aphis fabae, Aphis
forbesi, Aphis pomi, Aphis gossypii, Aphis grossulariae, Aphis
schneideri, Aphis spiraecola, Aphis sambuci, Acyrthosiphon pisum,
Aulacorthum solani, Bemisia argentifolii, Brachycaudus cardui,
Brachycaudus helichrysi, Brachycaudus persicae, Brachycaudus
prunicola, Brevicoryne brassicae, Capitophorus horni, Cerosipha
gossypii, Chaetosiphon fragaefolii, Cryptomyzus ribis, Dreyfusia
nordmannianae, Dreyfusia piceae, Dysaphis radicola, Dysaulacorthum
pseudosolani, Dysaphis plantaginea, Dysaphis pyri, Empoasca fabae,
Hyalopterus pruni, Hyperomyzus lactucae, Macrosiphum avenae,
Macrosiphum euphorbiae, Macrosiphon rosae, Megoura viciae,
Melanaphis pyrarius, Metopolophium dirhodum, Myzus persicae, Myzus
ascalonicus, Myzus cerasi, Myzus varians, Nasonovia ribis-nigri,
Nilaparvata lugens, Pemphigus bursarius, Perkinsiella saccharicida,
Phorodon humuli, Psylla mali, Psylla pini, Rhopalomyzus
ascalonicus, Rhopalosiphum maidis, Rhopalosiphum padi,
Rhopalosiphum insertum, Sappaphis mala, Sappaphis mali, Schizaphis
graminum, Schizoneura lanuginosa, Sitobion avenae, Trialeurodes
vaporariorum, Toxoptera aurantiiand, Viteus vitifolii, Cimex
lectularius, Cimex hemipterus, Reduvius senilis, Triatoma spp., and
Arilus critatus. ants, bees, wasps, sawflies (Hymenoptera), e.g.
Athalia rosae, Atta cephalotes, Atta capiguara, Atta cephalotes,
Atta laevigata, Atta robusta, Atta sexdens, Atta texana,
Crematogaster spp., Hoplocampa minuta, Hoplocampa testudinea,
Monomorium pharaonis, Solenopsis geminata, Solenopsis invicta,
Solenopsis richteri, Solenopsis xyloni, Pogonomyrmex barbatus,
Pogonomyrmex californicus, Pheidole megacephala, Dasymutilla
occidentalis, Bombus spp. Vespula squamosa, Paravespula vulgaris,
Paravespula pennsylvanica, Paravespula germanica, Dolichovespula
maculata, Vespa crabro, Polistes rubiginosa, Camponotus fioridanus,
and Linepithema humile, crickets, grasshoppers, locusts
(Orthoptera), e.g. Acheta domestica, Gryllotalpa gryllotalpa,
Locusta migratoria, Melanoplus bivittatus, Melanoplus femurrubrum,
Melanoplus mexicanus, Melanoplus sanguinipes, Melanoplus spretus,
Nomadacris septemfasciata, Schistocerca americana, Schistocerca
gregaria, Dociostaurus maroccanus, Tachycines asynamorus, Oedaleus
senegalensis, Zonozerus variegatus, Hieroglyphus daganensis,
Kraussaria angulifera, Calliptamus italicus, Chortoicetes
terminifera, and Locustana pardalina, Arachnoidea, such as
arachnids (Acarina), e.g. of the families Argasidae, Ixodidae and
Sarcoptidae, such as Amblyomma americanum, Amblyomma variegatum,
Amblyomma maculatum, Argas persicus, Boophilus annulatus, Boophilus
decoloratus, Boophilus microplus, Dermacentor silvarum, Dermacentor
andersoni, Dermacentor variabilis, Hyalomma truncatum, Ixodes
ricinus, Ixodes rubicundus, Ixodes scapularis, Ixodes holocyclus,
Ixodes pacificus, Ornithodorus moubata, Ornithodorus hermsi,
Ornithodorus turicata, Ornithonyssus bacoti, Otobius megnini,
Dermanyssus gallinae, Psoroptes ovis, Rhipicephalus sanguineus,
Rhipicephalus appendiculatus, Rhipicephalus evertsi, Sarcoptes
scabiei, and Eriophyidae spp. such as Aculus schlechtendali,
Phyllocoptrata oleivora and Eriophyes sheldoni; Tarsonemidae spp.
such as Phytonemus pallidus and Polyphagotarsonemus latus;
Tenuipalpidae spp. such as Brevipalpus phoenicis; Tetranychidae
spp. such as Tetranychus cinnabarinus, Tetranychus kanzawai,
Tetranychus pacificus, Tetranychus telarius and Tetranychus
urticae, Panonychus ulmi, Panonychus citri, and Oligonychus
pratensis; Araneida, e.g. Latrodectus mactans, and Loxosceles
reclusa, fleas (Siphonaptera), e.g. Ctenocephalides felis,
Ctenocephalides canis, Xenopsylla cheopis, Pulex irritans, Tunga
penetrans, and Nosopsyllus fasciatus, silverfish, firebrat
(Thysanura), e.g. Lepisma saccharina and Thermobia domestica,
centipedes (Chilopoda), e.g. Scutigera coleoptrata, millipedes
(Diplopoda), e.g. Narceus spp., Earwigs (Dermaptera), e.g.
forficula auricularia, lice (Phthiraptera), e.g. Pediculus humanus
capitis, Pediculus humanus corporis, Pthirus pubis, Haematopinus
eurysternus, Haematopinus suis, Linognathus vituli, Bovicola bovis,
Menopon gallinae, Menacanthus stramineus and Solenopotes
capillatus.
[0174] Plant parasitic nematodes such as root-knot nematodes,
Meloidogyne arenaria, Meloidogyne chitwoodi, Meloidogyne exigua,
Meloidogyne hapla, Meloidogyne incognita, Meloidogyne javanica and
other Meloidogyne species; cyst nematodes, Globodera rostochiensis,
Globodera pallida, Globodera tabacum and other Globodera species,
Heterodera avenae, Heterodera glycines, Heterodera schachtii,
Heterodera trifolii, and other Heterodera species; seed gall
nematodes, Anguina funesta, Anguina tritici and other Anguina
species; stem and foliar nematodes, Aphelenchoides besseyi,
Aphelenchoides fragariae, Aphelenchoides ritzemabosi and other
Aphelenchoides species; sting nematodes, Belonolaimus longicaudatus
and other Belonolaimus species; pine nematodes, Bursaphelenchus
xylophilus and other Bursaphelenchus species; ring nematodes,
Criconema species, Criconemella species, Criconemoides species, and
Mesocriconema species; stem and bulb nematodes, Ditylenchus
destructor, Ditylenchus dipsaci, Ditylenchus myceliophagus and
other Ditylenchus species; awl nematodes, Dolichodorus species;
spiral nematodes, Helicotylenchus dihystera, Helicotylenchus
multicinctus and other Helicotylenchus species, Rotylenchus
robustus and other Rotylenchus species; sheath nematodes,
Hemicycliophora species and Hemicriconemoides species;
Hirshmanniella species; lance nematodes, Hoplolaimus columbus,
Hoplolaimus galeatus and other Hoplolaimus species; false root-knot
nematodes, Nacobbus aberrans and other Nacobbus species; needle
nematodes, Longidorus elongates and other Longidorus species; pin
nematodes, Paratylenchus species; lesion nematodes, Pratylenchus
brachyurus, Pratylenchus coffeae, Pratylenchus curvitatus,
Pratylenchus goodeyi, Pratylencus neglectus, Pratylenchus
penetrans, Pratylenchus scribneri, Pratylenchus vulnus,
Pratylenchus zeae and other Pratylenchus species; Radinaphelenchus
cocophilus and other Radinaphelenchus species; burrowing nematodes,
Radopholus similis and other Radopholus species; reniform
nematodes, Rotylenchulus reniformis and other Rotylenchulus
species; Scutellonema species; stubby root nematodes, Trichodorus
primitivus and other Trichodorus species; Paratrichodorus minor and
other Paratrichodorus species; stunt nematodes, Tylenchorhynchus
claytoni, Tylenchorhynchus dubius and other Tylenchorhynchus
species and Merlinius species; citrus nematodes, Tylenchulus
semipenetrans and other Tylenchulus species; dagger nematodes,
Xiphinema americanum, Xiphinema index, Xiphinema diversicaudatum
and other Xiphinema species; and other plant parasitic nematode
species.
[0175] Moreover, the inventive mixtures are especially useful for
the control of Lepidoptera, Coleoptera, Diptera, Thysanoptera and
Hymenoptera.
[0176] In particular the inventive mixtures are useful for the
control of Thysanoptera and Hymenoptera, especially
Hymenoptera.
Formulations
[0177] The mixtures according to the present invention can be
converted into the customary formulations, for example solutions,
emulsions, suspensions, dusts, powders, pastes and granules. The
use form depends on the particular intended purpose; in each case,
it should ensure a fine and even distribution of the compounds
according to the invention.
[0178] The formulations are prepared in a known manner (see e.g.
for review U.S. Pat. No. 3,060,084, EP-A 707 445 (for liquid
concentrates), Browning, "Agglomeration", Chemical Engineering,
Dec. 4, 1967, 147-48, Perry's Chemical Engineer's Handbook, 4th
Ed., McGraw-Hill, New York, 1963, pages 8-57 and et seq. WO
91/13546, U.S. Pat. No. 4,172,714, U.S. Pat. No. 4,144,050, U.S.
Pat. No. 3,920,442, U.S. Pat. No. 5,180,587, U.S. Pat. No.
5,232,701, U.S. Pat. No. 5,208,030, GB 2,095,558, U.S. Pat. No.
3,299,566, Klingman, Weed Control as a Science, John Wiley and
Sons, Inc., New York, 1961, Hance et al., Weed Control Handbook,
8th Ed., Blackwell Scientific Publications, Oxford, 1989 and
Mollet, H., Grubemann, A., Formulation technology, Wiley VCH Verlag
GmbH, Weinheim (Germany), 2001, 2. D. A. Knowles, Chemistry and
Technology of Agrochemical Formulations, Kluwer Academic
Publishers, Dordrecht, 1998 (ISBN 0-7514-0443-8), for example by
extending the active compound with auxiliaries suitable for the
formulation of agrochemicals, such as solvents and/or carriers, if
desired emulsifiers, surfactants and dispersants, preservatives,
antifoaming agents, anti-freezing agents, for seed treatment
formulation also optionally gelling agents.
[0179] Examples of suitable solvents are water, aromatic solvents
(for example Solvesso products, xylene), paraffins (for example
mineral oil fractions), alcohols (for example methanol, butanol,
pentanol, benzyl alcohol), ketones (for example cyclohexanone,
gammabutyrolactone), pyrrolidones (NMP(N-methyl-pyrrolidone), NOP
(N-octylpyrrolidone)), acetates (glycol diacetate), glycols, fatty
acid dimethylamides, fatty acids and fatty acid esters. In
principle, solvent mixtures may also be used.
[0180] Suitable emulsifiers are nonionic and anionic emulsifiers
(for example polyoxyethylene fatty alcohol ethers, alkylsulfonates
and arylsulfonates).
[0181] Examples of dispersants are lignin-sulfite waste liquors and
methylcellulose.
[0182] Suitable surfactants used are alkali metal, alkaline earth
metal and ammonium salts of lignosulfonic acid, naphthalenesulfonic
acid, phenolsulfonic acid, dibutylnaphthalene-sulfonic acid,
alkylarylsulfonates, alkyl sulfates, alkylsulfonates, fatty alcohol
sulfates, fatty acids and sulfated fatty alcohol glycol ethers,
furthermore condensates of sulfonated naphthalene and naphthalene
derivatives with formaldehyde, condensates of naphthalene or of
naphthalenesulfonic acid with phenol and formaldehyde,
polyoxyethylene octylphenol ether, ethoxylated isooctylphenol,
octylphenol, nonylphenol, alkylphenol polyglycol ethers,
tributylphenyl polyglycol ether, tristearylphenyl polyglycol ether,
alkylaryl polyether alcohols, alcohol and fatty alcohol ethylene
oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl
ethers, ethoxylated polyoxypropyl-ene, lauryl alcohol polyglycol
ether acetal, sorbitol esters, lignosulfite waste liquors and
methylcellulose.
[0183] Substances which are suitable for the preparation of
directly sprayable solutions, emulsions, pastes or oil dispersions
are mineral oil fractions of medium to high boiling point, such as
kerosene or diesel oil, furthermore coal tar oils and oils of
vegetable or animal origin, aliphatic, cyclic and aromatic
hydrocarbons, for example toluene, xylene, paraffin,
tetrahydronaphthalene, alkylated naphthalenes or their derivatives,
methanol, ethanol, propanol, butanol, cyclohexanol, cyclohexanone,
isophorone, highly polar solvents, for example dimethyl sulfoxide,
N-methylpyrrolidone or water.
[0184] Also anti-freezing agents such as glycerin, ethylene glycol,
propylene glycol and bactericides such as can be added to the
formulation.
[0185] Suitable antifoaming agents are for example antifoaming
agents based on silicon or magnesium stearate.
[0186] A suitable preservative is e.g. dichlorophen.
[0187] An example of a gelling agent is carrageen
(Satiagel.RTM.)
[0188] Powders, materials for spreading and dustable products can
be prepared by mixing or concomitantly grinding the active
substances with a solid carrier.
[0189] Granules, for example coated granules, impregnated granules
and homogeneous granules, can be prepared by binding the active
compounds to solid carriers.
[0190] Examples of solid carriers are mineral earths such as silica
gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk,
bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate,
magnesium sulfate, magnesium oxide, ground synthetic materials,
fertilizers, such as, for example, ammonium sulfate, ammonium
phosphate, ammonium nitrate, ureas, and products of vegetable
origin, such as cereal meal, tree bark meal, wood meal and nutshell
meal, cellulose powders and other solid carriers.
[0191] In general, the formulations comprise from 0.01 to 95% by
weight, preferably from 0.1 to 90% by weight, of the active
compounds. In this case, the active compounds are employed in a
purity of from 90% to 100% by weight, preferably 95% to 100% by
weight (according to NMR spectrum).
[0192] For seed treatment purposes, respective formulations can be
diluted 2-10 fold leading to concentrations in the ready to use
preparations of 0.01 to 60% by weight active compounds by weight,
preferably 0.1 to 40% by weight.
[0193] The mixtures of the present invention can be used as such,
in the form of their formulations or the use forms prepared
therefrom, for example in the form of directly sprayable solutions,
powders, suspensions or dispersions, emulsions, oil dispersions,
pastes, dustable products, materials for spreading, or granules, by
means of spraying, atomizing, dusting, spreading or pouring. The
use forms depend entirely on the intended purposes; they are
intended to ensure in each case the finest possible distribution of
the active compounds according to the invention.
[0194] Aqueous use forms can be prepared from emulsion
concentrates, pastes or wettable powders (sprayable powders, oil
dispersions) by adding water. To prepare emulsions, pastes or oil
dispersions, the substances, as such or dissolved in an oil or
solvent, can be homogenized in water by means of a wetter,
tackifier, dispersant or emulsifier. However, it is also possible
to prepare concentrates composed of active substance, wetter,
tackifier, dispersant or emulsifier and, if appropriate, solvent or
oil, and such concentrates are suitable for dilution with
water.
[0195] The active compound concentrations in the ready-to-use
preparations can be varied within relatively wide ranges. In
general, they are from 0.0001 to 10%, preferably from 0.01 to 1%
per weight.
[0196] The active compound(s) may also be used successfully in the
ultra-low-volume process (ULV), it being possible to apply
formulations comprising over 95% by weight of active compound, or
even to apply the active compound without additives.
[0197] The following are examples of formulations:
[0198] 1. Products for dilution with water for foliar applications.
For seed treatment purposes, such products may be applied to the
seed diluted or undiluted.
[0199] A) Water-Soluble Concentrates (SL, LS)
[0200] 10 parts by weight of the active compound(s) are dissolved
in 90 parts by weight of water or a water-soluble solvent. As an
alternative, wetters or other auxiliaries are added. The active
compound(s) dissolve(s) upon dilution with water, whereby a
formulation with 10% (w/w) of active compound(s) is obtained.
[0201] B) Dispersible Concentrates (DC)
[0202] 20 parts by weight of the active compound(s) are dissolved
in 70 parts by weight of cyclohexanone with addition of 10 parts by
weight of a dispersant, for example polyvinylpyrrolidone. Dilution
with water gives a dispersion, whereby a formulation with 20% (w/w)
of active compound(s) is obtained.
[0203] C) Emulsifiable Concentrates (EC)
[0204] 15 parts by weight of the active compound(s) are dissolved
in 7 parts by weight of xylene with addition of calcium
dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5
parts by weight). Dilution with water gives an emulsion, whereby a
formulation with 15% (w/w) of active compound(s) is obtained.
[0205] D) Emulsions (EW, EO, ES)
[0206] 25 parts by weight of the active compound(s) are dissolved
in 35 parts by weight of xylene with addition of calcium
dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5
parts by weight). This mixture is introduced into 30 parts by
weight of water by means of an emulsifier machine (e.g.
Ultraturrax) and made into a homogeneous emulsion. Dilution with
water gives an emulsion, whereby a formulation with 25% (w/w) of
active compound(s) is obtained.
[0207] E) Suspensions (SC, OD, FS)
[0208] In an agitated ball mill, 20 parts by weight of the active
compound(s) are comminuted with addition of 10 parts by weight of
dispersants, wetters and 70 parts by weight of water or of an
organic solvent to give a fine active compound(s) suspension.
Dilution with water gives a stable suspension of the active
compound(s), whereby a formulation with 20% (w/w) of active
compound(s) is obtained.
[0209] F) Water-Dispersible Granules and Water-Soluble Granules
(WG, SG)
[0210] 50 parts by weight of the active compound(s) are ground
finely with addition of 50 parts by weight of dispersants and
wetters and made as water-dispersible or water-soluble granules by
means of technical appliances (for example extrusion, spray tower,
fluidized bed). Dilution with water gives a stable dispersion or
solution of the active compound(s), whereby a formulation with 50%
(w/w) of active compound(s) is obtained.
[0211] G) Water-Dispersible Powders and Water-Soluble Powders (WP,
SP, SS, WS)
[0212] 75 parts by weight of the active compound(s) are ground in a
rotor-stator mill with addition of 25 parts by weight of
dispersants, wetters and silica gel. Dilution with water gives a
stable dispersion or solution of the active compound(s), whereby a
formulation with 75% (w/w) of active compound(s) is obtained.
[0213] H) Gel-Formulation (GF)
[0214] In an agitated ball mill, 20 parts by weight of the active
compound(s) are comminuted with addition of 10 parts by weight of
dispersants, 1 part by weight of gelling agent wetters and 70 parts
by weight of water or of an organic solvent to give a fine active
compound(s) suspension. Dilution with water gives a stable
suspension of the active compound(s), whereby a formulation with
20% (w/w) of active compound(s) is obtained.
[0215] 2. Products to be applied undiluted for foliar applications.
For seed treatment purposes, such products may be applied to the
seed diluted or undiluted.
[0216] I) Dustable Powders (DP, DS)
[0217] 5 parts by weight of the active compound(s) are ground
finely and mixed intimately with 95 parts by weight of finely
divided kaolin. This gives a dustable product having 5% (w/w) of
active compound(s).
[0218] J) Granules (GR, FG, GG, MG)
[0219] 0.5 part by weight of the active compound(s) is ground
finely and associated with 95.5 parts by weight of carriers,
whereby a formulation with 0.5% (w/w) of active compound(s) is
obtained. Current methods are extrusion, spray-drying or the
fluidized bed. This gives granules to be applied undiluted for
foliar use.
[0220] K) ULV Solutions (UL)
[0221] 10 parts by weight of the active compound(s) are dissolved
in 90 parts by weight of an organic solvent, for example xylene.
This gives a product having 10% (w/w) of active compound(s), which
is applied undiluted for foliar use.
[0222] Various types of oils, wetters, adjuvants, herbicides,
fungicides, other pesticides, or bactericides may be added to the
active ingredients, if appropriate just immediately prior to use
(tank mix). These agents usually are admixed with the agents
according to the invention in a weight ratio of 1:10 to 10:1.
Applications
[0223] The compounds I and the one or more compound(s) II can be
applied simultaneously, that is jointly or separately, or in
succession, the sequence, in the case of separate application,
generally not having any effect on the result of the control
measures.
[0224] The mixtures of the invention are employed as such or in
form of compositions by treating the insects or the plants, plant
propagation materials, such as seeds, soil, surfaces, materials or
rooms to be protected from insecticidal attack with a
insecticidally effective amount of the active compounds. The
application can be carried out both before and after the infection
of the plants, plant propagation materials, such as seeds, soil,
surfaces, materials or rooms by the insects.
[0225] The compounds I and the one or more compound(s) II are
usually applied in a weight ratio of from 500:1 to 1:100,
preferably from 20:1 to 1:50, in particular from 5:1 to 1:20.
[0226] Depending on the desired effect, the application rates of
the mixtures according to the invention are from 5 g/ha to 2000
g/ha, preferably from 50 to 1500 g/ha, in particular from 50 to 750
g/ha.
[0227] The mixtures according to the invention are effective
through both contact and ingestion.
[0228] According to a preferred embodiment of the invention, the
mixtures according to the present invention are employed via soil
application. Soil application is especially favorable for use
against ants, termites, crickets, or cockroaches.
[0229] According to another preferred embodiment of the invention,
for use against non crop pests such as ants, termites, wasps,
flies, mosquitoes, crickets, locusts, or cockroaches the mixtures
according to the present invention are prepared into a bait
preparation.
[0230] The bait can be a liquid, a solid or a semisolid preparation
(e.g. a gel).
[0231] Another aspect of the present invention is when preparing
the mixtures, it is preferred to employ the pure active compounds I
and II, to which further active compounds, e.g. against harmful
fungi or having herbicidal activity, or growth-regulating agents or
fertilizers can be added.
[0232] Compositions of this invention may further contain other
active ingredients than those listed above. For example fungicides,
herbicides, fertilizers such as ammonium nitrate, urea, potash, and
superphosphate, phytotoxicants and plant growth regulators and
safeners. These additional ingredients may be used sequentially or
in combination with the above-described compositions, if
appropriate also added only immediately prior to use (tank mix).
For example, the plant(s) may be sprayed with a composition of this
invention either before or after being treated with other active
ingredients.
[0233] The mixtures according to the invention can be applied to
any and all developmental stages, such as egg, larva, pupa, and
adult. The pests may be controlled by contacting the target pest,
its food supply, habitat, breeding ground or its locus with a
pesticidally effective amount of the inventive mixtures or of
compositions comprising the mixtures. "Locus" means a plant, seed,
soil, area, material or environment in which a pest is growing or
may grow.
[0234] In general, "pesticidally effective amount" means the amount
of the inventive mixtures or of compositions comprising the
mixtures needed to achieve an observable effect on growth,
including the effects of necrosis, death, retardation, prevention,
and removal, destruction, or otherwise diminishing the occurrence
and activity of the target organism. The pesticidally effective
amount can vary for the various mixtures and/or compositions used
in the invention. A pesticidally effective amount of the mixtures
and/or compositions will also vary according to the prevailing
conditions such as desired pesticidal effect and duration, weather,
target species, locus, mode of application, and the like.
[0235] The inventive mixtures or compositions of these mixtures can
also be employed for protecting plants from attack or infestation
by insects, acarids or nematodes comprising contacting a plant, or
soil or water in which the plant is growing.
[0236] The inventive mixtures are effective through both contact
(via soil, glass, wall, bed net, carpet, plant parts or animal
parts), and ingestion (bait, or plant part) and through
trophallaxis and transfer.
[0237] Preferred application methods are into water bodies, via
soil, cracks and crevices, pastures, manure piles, sewers, into
water, on floor, wall, or by perimeter spray application and
bait.
[0238] According to another preferred embodiment of the invention,
for use against non crop pests such as ants, termites, wasps,
flies, mosquitoes, crickets, locusts, or cockroaches the inventive
mixtures are prepared into a bait preparation.
[0239] The bait can be a liquid, a solid or a semisolid preparation
(e.g. a gel). The bait employed in the composition is a product
which is sufficiently attractive to incite insects such as ants,
termites, wasps, flies, mosquitoes, crickets etc. or cockroaches to
eat it.
[0240] This attractant may be chosen from feeding stimulants or
para and/or sex pheromones readily known in the art.
[0241] Methods to control infectious diseases transmitted by
insects (e.g. malaria, dengue and yellow fever, lymphatic
filariasis, and leishmaniasis) with the inventive mixtures and
their respective compositions also comprise treating surfaces of
huts and houses, air spraying and impregnation of curtains, tents,
clothing items, bed nets, tsetse-fly trap or the like. Insecticidal
compositions for application to fibers, fabric, knitgoods,
nonwovens, netting material or foils and tarpaulins preferably
comprise a composition including the inventive mixtures, optionally
a repellent and at least one binder.
[0242] The inventive mixtures and the compositions comprising them
can be used for protecting wooden materials such as trees, board
fences, sleepers, etc. and buildings such as houses, outhouses,
factories, but also construction materials, furniture, leathers,
fibers, vinyl articles, electric wires and cables etc. from ants
and/or termites, and for controlling ants and termites from doing
harm to crops or human being (e.g. when the pests invade into
houses and public facilities).
[0243] In the case of soil treatment or of application to the pests
dwelling place or nest, the quantity of active ingredient(s) ranges
from 0.0001 to 500 g per 100 m.sup.2, preferably from 0.001 to 20 g
per 100 m.sup.2.
[0244] Customary application rates in the protection of materials
are, for example, from 0.01 g to 1000 g of active compound(s) per
m.sup.2 treated material, desirably from 0.1 g to 50 g per
m.sup.2.
[0245] Insecticidal compositions for use in the impregnation of
materials typically contain from 0.001 to 95 weight %, preferably
from 0.1 to 45 weight %, and more preferably from 1 to 25 weight %
of at least one repellent and/or insecticide.
[0246] For use in bait compositions, the typical content of active
ingredient(s) is from 0.0001 weight % to 15 weight %, desirably
from 0.001 weight % to 5% weight % of active compound. The
composition used may also comprise other additives such as a
solvent of the active material, a flavoring agent, a preserving
agent, a dye or a bitter agent. Its attractiveness may also be
enhanced by a special color, shape or texture.
[0247] For use in spray compositions, the content of the mixture of
the active ingredients is from 0.001 to 80 weights %, preferably
from 0.01 to 50 weight % and most preferably from 0.01 to 15 weight
%.
[0248] For use in treating crop plants, the rate of application of
the mixture of the active ingredients of this invention may be in
the range of 0.1 g to 4000 g per hectare, desirably from 25 g to
600 g per hectare, more desirably from 50 g to 500 g per
hectare.
[0249] In the context of the present invention, the term plant
refers to an entire plant, a part of the plant or the plant
propagation material.
[0250] The mixtures of the present invention and the compositions
comprising them are particularly important in the control of a
multitude of insects on various cultivated plants.
[0251] Plants which can be treated with the inventive mixtures
include all genetically modified plants or transgenic plants, e.g.
crops which tolerate the action of herbicides or fungicides or
insecticides owing to breeding, including genetic engineering
methods, or plants which have modified characteristics in
comparison with existing plants, which can be generated for example
by traditional breeding methods and/or the generation of mutants,
or by recombinant procedures.
[0252] The term "plant propagation material" is to be understood to
denote all the generative parts of the plant such as seeds and
vegetative plant material such as cuttings and tubers (e. g.
potatoes), which can be used for the multiplication of the plant.
This includes seeds, roots, fruits, tubers, bulbs, rhizomes,
shoots, sprouts and other parts of plants. Seedlings and young
plants, which are to be transplanted after germination or after
emergence from soil, may also be mentioned. These young plants may
also be protected before transplantation by a total or partial
treatment by immersion or pouring.
[0253] The term "cultivated plants" is to be understood as
including plants which have been modified by breeding, mutagenesis
or genetic engineering. Genetically modified plants are plants,
which genetic material has been so modified by the use of
recombinant DNA techniques that under natural circumstances cannot
be obtained by cross breeding, mutations or natural recombination.
Typically, one or more genes have been integrated into the genetic
material of a genetically modified plant in order to improve
certain properties of the plant.
[0254] The term "cultivated plants" is to be understood also
including plants that have been rendered tolerant to applications
of specific classes of herbicides, such as hydroxy-phenylpyruvate
dioxygenase (HPPD) inhibitors; acetolactate synthase (ALS)
inhibitors, such as sulfonyl ureas (see e. g. U.S. Pat. No.
6,222,100, WO 01/82685, WO 00/26390, WO 97/41218, WO 98/02526, WO
98/02527, WO 04/106529, WO 05/20673, WO 03/14357, WO 03/13225, WO
03/14356, WO 04/16073) or imidazolinones (see e. g. U.S. Pat. No.
6,222,100, WO 01/82685, WO 00/26390, WO 97/41218, WO 98/02526, WO
98/02527, WO 04/106529, WO 05/20673, WO 03/14357, WO 03/13225, WO
03/14356, WO 04/16073); enolpyruvylshikimate-3-phosphate synthase
(EPSPS) inhibitors, such as glyphosate (see e. g. WO 92/00377);
glutamine synthetase (GS) inhibitors, such as glufosinate (see e.
g. EP-A-0242236, EP-A-242246) or oxynil herbicides (see e. g. U.S.
Pat. No. 5,559,024) as a result of conventional methods of breeding
or genetic engineering. Several cultivated plants have been
rendered tolerant to herbicides by conventional methods of breeding
(mutagenesis), for example Clearfield.RTM. summer rape (Canola)
being tolerant to imidazolinones, e. g. imazamox. Genetic
engineering methods have been used to render cultivated plants,
such as soybean, cotton, corn, beets and rape, tolerant to
herbicides, such as glyphosate and glufosinate, some of which are
commercially available under the trade names RoundupReady.RTM.
(glyphosate) and LibertyLink.RTM. (glufosinate).
[0255] The term "cultivated plants" is to be understood also
including plants that are by the use of recombinant DNA techniques
capable to synthesize one or more insecticidal proteins, especially
those known from the bacterial genus Bacillus, particularly from
Bacillus thuringiensis, such as a-endotoxins, e. g. CryIA(b),
CryIA(c), CryIF, CryIF(a2), CryIIA(b), CryIIIA, CryIIIB(b1) or
Cry9c; vegetative insecticidal proteins (VIP), e. g. VIP 1, VIP2,
VIP3 or VIP3A; insecticidal proteins of bacteria colonizing
nematodes, for example Photorhabdus spp. or Xenorhabdus spp.;
toxins produced by animals, such as scorpion toxins, arachnid
toxins, wasp toxins, or other insect-specific neurotoxins; toxins
produced by fungi, such Streptomycetes toxins, plant lectins, such
as pea or barley lectins; agglutinins; proteinase inhibitors, such
as trypsin inhibitors, serine protease inhibitors, patatin,
cystatin or papain inhibitors; ribosome-inactivating proteins
(RIP), such as ricin, maize-RIP, abrin, luffin, saporin or bryodin;
steroid metabolism enzymes, such as 3-hydroxysteroid oxidase,
ecdysteroid-IDP-glycosyl-transferase, cholesterol oxidases,
ecdysone inhibitors or HMG-CoA-reductase; ion channel blockers,
such as blockers of sodium or calcium channels; juvenile hormone
esterase; diuretic hormone receptors (helicokinin receptors);
stilben synthase, bibenzyl synthase, chitinases or glucanases. In
the context of the present invention these insecticidal proteins or
toxins are to be understood expressly also as pre-toxins, hybrid
proteins, truncated or otherwise modified proteins. Hybrid proteins
are characterized by a new combination of protein domains, (see,
for example WO 02/015701). Further examples of such toxins or
genetically-modified plants capable of synthesizing such toxins are
dis-closed, for example, in EP-A 374 753, WO 93/007278, WO
95/34656, EP-A 427 529, EP-A 451 878, WO 03/018810 and WO
03/052073. The methods for producing such genetically modified
plants are generally known to the person skilled in the art and are
described, for example, in the publications mentioned above. These
insecticidal proteins contained in the genetically modified plants
impart to the plants producing these proteins tolerance to harmful
pests from all taxonomic groups of insects, especially to beetles
(Coeloptera), two-winged insects (Diptera), and butterflies
(Lepidoptera).
[0256] The term "cultivated plants" is to be understood also
including plants that are by the use of recombinant DNA techniques
capable to synthesize one or more proteins to in-crease the
resistance or tolerance of those plants to bacterial, viral or
fungal pathogens. Examples of such proteins are the so-called
"pathogenesis-related proteins" (PR proteins, see, for example EP-A
0 392 225), plant disease resistance genes (for example potato
cultivars, which express resistance genes acting against
Phytophthora infestans derived from the mexican wild potato Solanum
bulbocastanum) or T4-lyso-zym (e. g. potato cultivars capable of
synthesizing these proteins with increased resistance against
bacteria such as Erwinia amylvora). The methods for producing such
genetically modified plants are generally known to the person
skilled in the art and are described, for example, in the
publications mentioned above.
[0257] The term "cultivated plants" is to be understood also
including plants that are by the use of recombinant DNA techniques
capable to synthesize one or more proteins to increase the
productivity (e. g. bio mass production, grain yield, starch
content, oil content or protein content), tolerance to drought,
salinity or other growth-limiting environ-mental factors or
tolerance to pests and fungal, bacterial or viral pathogens of
those plants.
[0258] The term "cultivated plants" is to be understood also
including plants that contain by the use of recombinant DNA
techniques a modified amount of substances of content or new
substances of content, specifically to improve human or animal
nutrition, for ex-ample oil crops that produce health-promoting
long-chain omega-3 fatty acids or unsaturated omega-9 fatty acids
(e. g. Nexera.degree. rape).
[0259] The term "cultivated plants" is to be understood also
including plants that contain by the use of recombinant DNA
techniques a modified amount of substances of content or new
substances of content, specifically to improve raw material
production, for example potatoes that produce increased amounts of
amylopectin (e. g. Amflora.degree. potato).
[0260] Some of the inventive mixtures have systemic action and can
therefore be used for the protection of the plant shoot against
foliar pests as well as for the treatment of the seed and roots
against soil pests.
Seed Treatment
[0261] The mixtures according to the present invention are therfore
suitable for the treatment of seeds in order to protect the seed
from insect pest, in particular from soil-living insect pests and
the resulting plant's roots and shoots against soil pests and
foliar insects. The protection of the resulting plant's roots and
shoots is preferred.
[0262] More preferred is the protection of resulting plant's shoots
from piercing and sucking insects.
[0263] The present invention therefore comprises a method for the
protection of seeds from insects, in particular from soil insects
and of the seedlings' roots and shoots from insects, in particular
from soil and foliar insects, said method comprising contacting the
seeds before sowing and/or after pregermination with mixtures
according to the present invention. Particularly preferred is a
method, wherein the plant's roots and shoots are protected, more
preferably a method, wherein the plants shoots are protected form
piercing and sucking insects, most preferably a method, wherein the
plants shoots are protected from aphids.
[0264] The term seed embraces seeds and plant propagules of all
kinds including but not limited to true seeds, seed pieces,
suckers, corms, bulbs, fruit, tubers, grains, cuttings, cut shoots
and the like and means in a preferred embodiment true seeds.
[0265] The term seed treatment comprises all suitable seed
treatment techniques known in the art, such as seed dressing, seed
coating, seed dusting, seed soaking and seed pelleting.
[0266] The present invention also comprises seeds coated with or
containing the active compound(s). The term "coated with and/or
containing" generally signifies that the active ingredient(s) are
for the most part on the surface of the propagation product at the
time of application, although a greater or lesser part of the
ingredient may penetrate into the propagation product, depending on
the method of application. When the said propagation product are
(re)planted, it may absorb the active ingredient.
[0267] Suitable seeds are seeds of cereals, root crops, oil crops,
vegetables, spices, ornamentals, for example seed of durum and
other wheat, barley, oats, rye, maize (fodder maize and sugar
maize/sweet and field corn), soybeans, oil crops, crucifers,
cotton, sunflowers, bananas, rice, oilseed rape, turnip rape,
sugarbeet, fodder beet, eggplants, potatoes, grass, lawn, turf,
fodder grass, tomatoes, leeks, pumpkin/squash, cabbage, iceberg
lettuce, pepper, cucumbers, melons, Brassica species, melons,
beans, peas, garlic, onions, carrots, tuberous plants such as
potatoes, sugar cane, tobacco, grapes, petunias,
geranium/pelargoniums, pansies and impatiens.
[0268] In addition, the mixtures according to the invention may
also be used for the treatment seeds from plants, which tolerate
the action of herbicides or fungicides or insecticides owing to
breeding, including genetic engineering methods.
[0269] For example, the active mixtures can be employed in
treatment of seeds from plants, which are resistant to herbicides
from the group consisting of the sulfonylureas, imidazolinones,
glufosinate-ammonium or glyphosate-isopropylammonium and analogous
active substances (see for example, EP-A-0242236, EP-A-242246) (WO
92/00377) (EP-A-0257993, U.S. Pat. No. 5,013,659) or in transgenic
crop plants, for example cotton, with the capability of producing
Bacillus thuringiensis toxins (Bt toxins) which make the plants
resistant to certain pests (EP-A-0142924, EP-A-0193259),
[0270] Furthermore, the mixtures according to the present invention
can be used also for the treatment of seeds from plants, which have
modified characteristics in comparison with existing plants
consist, which can be generated for example by traditional breeding
methods and/or the generation of mutants, or by recombinant
procedures). For example, a number of cases have been described of
recombinant modifications of crop plants for the purpose of
modifying the starch synthesized in the plants (e.g. WO 92/11376,
WO 92/14827, WO 91/19806) or of transgenic crop plants having a
modified fatty acid composition (WO 91/13972).
[0271] The seed treatment application of the mixtures is carried
out by spraying or by dusting the seeds before sowing of the plants
and before emergence of the plants.
[0272] In the treatment of seeds the corresponding formulations are
applied by treating the seeds with an effective amount of the
mixture according to the present invention. Herein, the application
rates of the active compound(s) are generally from 0.1 g to 10 kg
per 100 kg of seed, preferably from 1 g to 5 kg per 100 kg of seed,
in particular from 1 g to 2.5 kg per 100 kg of seed. For specific
crops such as lettuce the rate can be higher.
[0273] Compositions, which are especially useful for seed treatment
are e.g.: [0274] A Soluble concentrates (SL, LS) [0275] D Emulsions
(EW, EO, ES) [0276] E Suspensions (SC, OD, FS) [0277] F
Water-dispersible granules and water-soluble granules (WG, SG)
[0278] G Water-dispersible powders and water-soluble powders (WP,
SP, WS) [0279] H Gel-Formulations (GF) [0280] I Dustable powders
(DP, DS)
[0281] Conventional seed treatment formulations include for example
flowable concentrates FS, solutions LS, powders for dry treatment
DS, water dispersible powders for slurry treatment WS,
water-soluble powders SS and emulsion ES and EC and gel formulation
GF. These formulations can be applied to the seed diluted or
undiluted. Application to the seeds is carried out before sowing,
either directly on the seeds or after having pregerminated the
latter
[0282] In a preferred embodiment a FS formulation is used for seed
treatment. Typically, a FS formulation may comprise 1-800 g/l of
active ingredient(s), 1-200 g/l Surfactant, 0 to 200 g/l
antifreezing agent, 0 to 400 g/l of binder, 0 to 200 g/l of a
pigment and up to 1 liter of a solvent, preferably water.
[0283] Preferred FS formulations of compounds of formula I for seed
treatment usually comprise from 0.1 to 80% by weight (1 to 800 g/l)
of the active ingredient(s), from 0.1 to 20% by weight (1 to 200
g/l) of at least one surfactant, e.g. 0.05 to 5% by weight of a
wetter and from 0.5 to 15% by weight of a dispersing agent, up to
20% by weight, e.g. from 5 to 20% of an anti-freeze agent, from 0
to 15% by weight, e.g. 1 to 15% by weight of a pigment and/or a
dye, from 0 to 40% by weight, e.g. 1 to 40% by weight of a binder
(sticker/adhesion agent), optionally up to 5% by weight, e.g. from
0.1 to 5% by weight of a thickener, optionally from 0.1 to 2% of an
anti-foam agent, and optionally a preservative such as a biocide,
antioxidant or the like, e.g. in an amount from 0.01 to 1% by
weight and a filler/vehicle up to 100% by weight.
[0284] Seed Treatment formulations may additionally also comprise
binders and optionally colorants.
[0285] Binders can be added to improve the adhesion of the active
materials on the seeds after treatment. Suitable binders are block
copolymers EO/PO surfactants but also polyvinylalcoholsl,
polyvinylpyrrolidones, polyacrylates, polymethacrylates,
polybutenes, polyisobutylenes, polystyrene, polyethyleneamines,
polyethyleneamides, polyethyleneimines (Lupasol.RTM.,
Polymin.RTM.), polyethers, polyurethans, polyvinylacetate, tylose
and copolymers derived from these polymers.
[0286] Optionally, also colorants can be included in the
formulation. Suitable colorants or dyes for seed treatment
formulations are Rhodamin B, C.I. Pigment Red 112, C.I. Solvent Red
1, pigment blue 15:4, pigment blue 15:3, pigment blue 15:2, pigment
blue 15:1, pigment blue 80, pigment yellow 1, pigment yellow 13,
pigment red 112, pigment red 48:2, pigment red 48:1, pigment red
57:1, pigment red 53:1, pigment orange 43, pigment orange 34,
pigment orange 5, pigment green 36, pigment green 7, pigment white
6, pigment brown 25, basic violet 10, basic violet 49, acid red 51,
acid red 52, acid red 14, acid blue 9, acid yellow 23, basic red
10, basic red 108.
[0287] The invention also relates to seed comprising mixtures
according to the present invention. The amount of the compound I or
the agriculturally useful salt thereof will in general vary from
0.1 g to 10 kg per 100 kg of seed, preferably from 1 g to 5 kg per
100 kg of seed, in particular from 1 g to 1000 g per 100 kg of
seed.
Animal Health
[0288] The mixtures of the present invention are in particular also
suitable for being used for combating parasites in and on
animals.
[0289] An object of the present invention is therefore also to
provide new methods to control parasites in and on animals. Another
object of the invention is to provide safer pesticides for animals.
Another object of the invention is further to provide pesticides
for animals that may be used in lower doses than existing
pesticides. And another object of the invention is to provide
pesticides for animals, which provide a long residual control of
the parasites.
[0290] The invention also relates to compositions containing a
parasiticidally effective amount of compounds of formula I or the
enantiomers or veterinarily acceptable salts thereof and an
acceptable carrier, for combating parasites in and on animals.
[0291] The present invention also provides a method for treating,
controlling, preventing and protecting animals against infestation
and infection by parasites, which comprises orally, topically or
parenterally administering or applying to the animals a
parasiticidally effective amount of mixture of the present
invention or a composition comprising it.
[0292] The invention also provides a process for the preparation of
a composition for treating, controlling, preventing or protecting
animals against infestation or infection by parasites which
comprises a parasiticidally effective amount of a mixture of the
present invention or a composition comprising it.
[0293] Activity of compounds against agricultural pests does not
suggest their suitability for control of endo- and ectoparasites in
and on animals which requires, for example, low, non-emetic dosages
in the case of oral application, metabolic compatibility with the
animal, low toxicity, and a safe handling.
[0294] Surprisingly it has now been found that mixtures of the
present invention are suitable for combating endo- and
ectoparasites in and on animals.
[0295] Mixtures of the present invention and compositions
comprising them are preferably used for controlling and preventing
infestations and infections animals including warm-blooded animals
(including humans) and fish. They are for example suitable for
controlling and preventing infestations and infections in mammals
such as cattle, sheep, swine, camels, deer, horses, pigs, poultry,
rabbits, goats, dogs and cats, water buffalo, donkeys, fallow deer
and reindeer, and also in fur-bearing animals such as mink,
chinchilla and raccoon, birds such as hens, geese, turkeys and
ducks and fish such as fresh- and salt-water fish such as trout,
carp and eels.
[0296] Mixtures of the present invention and compositions
comprising them are preferably used for controlling and preventing
infestations and infections in domestic animals, such as dogs or
cats.
[0297] Infestations in warm-blooded animals and fish include, but
are not limited to, lice, biting lice, ticks, nasal bots, keds,
biting flies, muscoid flies, flies, myiasitic fly larvae, chiggers,
gnats, mosquitoes and fleas.
[0298] The mixtures of the present invention and compositions
comprising them are suitable for systemic and/or non-systemic
control of ecto- and/or endoparasites. They are active against all
or some stages of development.
[0299] The mixtures of the present invention are especially useful
for combating ectoparasites.
[0300] The mixture of the present invention are especially useful
for combating parasites of the following orders and species,
respectively:
fleas (Siphonaptera), e.g. Ctenocephalides felis, Ctenocephalides
canis, Xenopsylla cheopis, Pulex irritans, Tunga penetrans, and
Nosopsyllus fasciatus, cockroaches (Blattaria-Blattodea), e.g.
Blattella germanica, Blattella asahinae, Periplaneta americana,
Periplaneta japonica, Periplaneta brunnea, Periplaneta fuligginosa,
Periplaneta australasiae, and Blatta orientalis, flies, mosquitoes
(Diptera), e.g. Aedes aegypti, Aedes albopictus, Aedes vexans,
Anastrepha ludens, Anopheles maculipennis, Anopheles crucians,
Anopheles albimanus, Anopheles gambiae, Anopheles freeborni,
Anopheles leucosphyrus, Anopheles minimus, Anopheles
quadrimaculatus, Calliphora vicina, Chrysomya bezziana, Chrysomya
hominivorax, Chrysomya macellaria, Chrysops discalis, Chrysops
silacea, Chrysops atlanticus, Cochliomyia hominivorax, Cordylobia
anthropophaga, Culicoides furens, Culex pipiens, Culex nigripalpus,
Culex quinquefasciatus, Culex tarsalis, Culiseta inornata, Culiseta
melanura, Dermatobia hominis, Fannia canicularis, Gasterophilus
intestinalis, Glossina morsitans, Glossina palpalis, Glossina
fuscipes, Glossina tachinoides, Haematobia irritans, Haplodiplosis
equestris, Hippelates spp., Hypoderma lineata, Leptoconops torrens,
Lucilia caprina, Lucilia cuprina, Lucilia sericata, Lycoria
pectoralis, Mansonia spp., Musca domestica, Muscina stabulans,
Oestrus ovis, Phlebotomus argentipes, Psorophora columbiae,
Psorophora discolor, Prosimulium mixtum, Sarcophaga
haemorrhoidalis, Sarcophaga sp., Simulium vittatum, Stomoxys
calcitrans, Tabanus bovinus, Tabanus atratus, Tabanus lineola, and
Tabanus similis, lice (Phthiraptera), e.g. Pediculus humanus
capitis, Pediculus humanus corporis, Pthirus pubis, Haematopinus
eurysternus, Haematopinus suis, Linognathus vituli, Bovicola bovis,
Menopon gallinae, Menacanthus stramineus and Solenopotes
capillatus. ticks and parasitic mites (Parasitiformes): ticks
(Ixodida), e.g. Ixodes scapularis, Ixodes holocyclus, Ixodes
pacificus, Rhiphicephalus sanguineus, Dermacentor andersoni,
Dermacentor variabilis, Amblyomma americanum, Amblyomma maculatum,
Ornithodorus hermsi, Ornithodorus turicata and parasitic mites
(Mesostigmata), e.g. Ornithonyssus bacoti and Dermanyssus gallinae,
Actinedida (Prostigmata) and Acaridida (Astigmata) e.g. Acarapis
spp., Cheyletiella spp., Ornithocheyletia spp., Myobia spp.,
Psorergates spp., Demodex spp., Trombicula spp., Listrophorus spp.,
Acarus spp., Tyrophagus spp., Caloglyphus spp., Hypodectes spp.,
Pterolichus spp., Psoroptes spp., Chorioptes spp., Otodectes spp.,
Sarcoptes spp., Notoedres spp., Knemidocoptes spp., Cytodites spp.,
and Laminosioptes spp, Bugs (Heteropterida): Cimex lectularius,
Cimex hemipterus, Reduvius senilis, Triatoma spp., Rhodnius ssp.,
Panstrongylus ssp. and Arilus critatus, Anoplurida, e.g.
Haematopinus spp., Linognathus spp., Pediculus spp., Phtirus spp.,
and Solenopotes spp, Mallophagida (suborders Arnblycerina and
Ischnocerina), e.g. Trimenopon spp., Menopon spp., Trinoton spp.,
Bovicola spp., Werneckiella spp., Lepikentron spp., Trichodectes
spp., and Felicola spp,
Roundworms Nematoda:
[0301] Wipeworms and Trichinosis (Trichosyringida), e.g.
Trichinellidae (Trichinella spp.), (Trichuridae) Trichuris spp.,
Capillaria spp, Rhabditida, e.g. Rhabditis spp, Strongyloides spp.,
Helicephalobus spp, Strongylida, e.g. Strongylus spp., Ancylostoma
spp., Necator americanus, Bunostomum spp. (Hookworm),
Trichostrongylus spp., Haemonchus contortus., Ostertagia spp.,
Cooperia spp., Nematodirus spp., Dictyocaulus spp., Cyathostoma
spp., Oesophagostomum spp., Stephanurus dentatus, Ollulanus spp.,
Chabertia spp., Stephanurus dentatus, Syngamus trachea, Ancylostoma
spp., Uncinaria spp., Globocephalus spp., Necator spp.,
Metastrongylus spp., Muellerius capillaris, Protostrongylus spp.,
Angiostrongylus spp., Parelaphostrongylus spp. Aleurostrongylus
abstrusus, and Dioctophyma renale, Intestinal roundworms
(Ascaridida), e.g. Ascaris lumbricoides, Ascaris suum, Ascaridia
galli, Parascaris equorum, Enterobius vermicularis (Threadworm),
Toxocara canis, Toxascaris leonine, Skrjabinema spp., and Oxyuris
equi, Camallanida, e.g. Dracunculus medinensis (guinea worm)
Spirurida, e.g. Thelazia spp. Wuchereria spp., Brugia spp.,
Onchocerca spp., Dirofilari spp.a, Dipetalonema spp., Setaria spp.,
Elaeophora spp., Spirocerca lupi, and Habronema spp., Thorny headed
worms (Acanthocephala), e.g. Acanthocephalus spp.,
Macracanthorhynchus hirudinaceus and Oncicola spp,
Planarians (Plathelminthes):
[0302] Flukes (Trematoda), e.g. Faciola spp., Fascioloides magna,
Paragonimus spp., Dicrocoelium spp., Fasciolopsis buski, Clonorchis
sinensis, Schistosoma spp., Trichobilharzia spp., Alaria alata,
Paragonimus spp., and Nanocyetes spp,
Cercomeromorpha, in particular Cestoda (Tapeworms), e.g.
Diphyllobothrium spp., Tenia spp., Echinococcus spp., Dipylidium
caninum, Multiceps spp., Hymenolepis spp., Mesocestoides spp.,
Vampirolepis spp., Moniezia spp., Anoplocephala spp., Sirometra
spp., Anoplocephala spp., and Hymenolepis spp.
[0303] The mixtures of the present invention and compositions
containing them are particularly useful for the control of pests
from the orders Diptera, Siphonaptera and Ixodida.
[0304] Moreover, the use of mixtures of the present invention and
compositions containing them for combating mosquitoes is especially
preferred.
[0305] The use of mixtures of the present invention and
compositions containing them for combating flies is a further
preferred embodiment of the present invention.
[0306] Furthermore, the use of the mixtures of the present
invention and compositions containing them for combating fleas is
especially preferred.
[0307] The use of the mixtures of the present invention and
compositions containing them for combating ticks is a further
preferred embodiment of the present invention.
[0308] The mixtures of the present invention also are especially
useful for combating endoparasites (roundworms nematoda, thorny
headed worms and planarians).
[0309] Administration can be carried out both prophylactically and
therapeutically.
[0310] Administration of the active compounds is carried out
directly or in the form of suitable preparations, orally,
topically/dermally or parenterally.
[0311] For oral administration to warm-blooded animals, the
mixtures of the present invention may be formulated as animal
feeds, animal feed premixes, animal feed concentrates, pills,
solutions, pastes, suspensions, drenches, gels, tablets, boluses
and capsules. In addition, the mixtures of the present invention
may be administered to the animals in their drinking water. For
oral administration, the dosage form chosen should provide the
animal with 0.01 mg/kg to 100 mg/kg of animal body weight per day
of the formula I compound, preferably with 0.5 mg/kg to 100 mg/kg
of animal body weight per day.
[0312] Alternatively, the mixtures of the present invention may be
administered to animals parenterally, for example, by intraruminal,
intramuscular, intravenous or subcutaneous injection. The formula I
compounds may be dispersed or dissolved in a physiologically
acceptable carrier for subcutaneous injection. Alternatively, the
mixtures of the present invention may be formulated into an implant
for subcutaneous administration. In addition the formula I compound
may be transdermally administered to animals. For parenteral
administration, the dosage form chosen should provide the animal
with 0.01 mg/kg to 100 mg/kg of animal body weight per day of the
active compounds.
[0313] The mixtures of the present invention may also be applied
topically to the animals in the form of dips, dusts, powders,
collars, medallions, sprays, shampoos, spot-on and pour-on
formulations and in ointments or oil-in-water or water-in-oil
emulsions. For topical application, dips and sprays usually contain
0.5 ppm to 5,000 ppm and preferably 1 ppm to 3,000 ppm of the
active compounds. In addition, the active compound mixtures may be
formulated as ear tags for animals, particularly quadrupeds such as
cattle and sheep.
[0314] Suitable preparations are: [0315] Solutions such as oral
solutions, concentrates for oral administration after dilution,
solutions for use on the skin or in body cavities, pouring-on
formulations, gels; [0316] Emulsions and suspensions for oral or
dermal administration; semi-solid preparations; [0317] Formulations
in which the active compound is processed in an ointment base or in
an oil-in-water or water-in-oil emulsion base; [0318] Solid
preparations such as powders, premixes or concentrates, granules,
pellets, tablets, boluses, capsules; aerosols and inhalants, and
active compound-containing shaped articles.
[0319] Compositions suitable for injection are prepared by
dissolving the active ingredient in a suitable solvent and
optionally adding further ingredients such as acids, bases, buffer
salts, preservatives, and solubilizers. The solutions are filtered
and filled sterile.
[0320] Suitable solvents are physiologically tolerable solvents
such as water, alkanols such as ethanol, butanol, benzyl alcohol,
glycerol, propylene glycol, polyethylene glycols,
N-methyl-pyrrolidone, 2-pyrrolidone, and mixtures thereof.
[0321] The active compounds can optionally be dissolved in
physiologically tolerable vegetable or synthetic oils which are
suitable for injection.
[0322] Suitable solubilizers are solvents which promote the
dissolution of the active compound in the main solvent or prevent
its precipitation. Examples are polyvinylpyrrolidone, polyvinyl
alcohol, polyoxyethylated castor oil, and polyoxyethylated sorbitan
ester.
[0323] Suitable preservatives are benzyl alcohol, trichlorobutanol,
p-hydroxybenzoic acid esters, and n-butanol.
[0324] Oral solutions are administered directly. Concentrates are
administered orally after prior dilution to the use concentration.
Oral solutions and concentrates are prepared according to the state
of the art and as described above for injection solutions, sterile
procedures not being necessary.
[0325] Solutions for use on the skin are trickled on, spread on,
rubbed in, sprinkled on or sprayed on.
[0326] Solutions for use on the skin are prepared according to the
state of the art and according to what is described above for
injection solutions, sterile procedures not being necessary.
[0327] Further suitable solvents are polypropylene glycol, phenyl
ethanol, phenoxy ethanol, ester such as ethyl or butyl acetate,
benzyl benzoate, ethers such as alkyleneglycol alkylether, e.g.
dipropylenglycol monomethylether, ketons such as acetone,
methylethylketone, aromatic hydrocarbons, vegetable and synthetic
oils, dimethylformamide, dimethylacetamide, transcutol, solketal,
propylencarbonate, and mixtures thereof
[0328] It may be advantageous to add thickeners during preparation.
Suitable thickeners are inorganic thickeners such as bentonites,
colloidal silicic acid, aluminium monostearate, organic thickeners
such as cellulose derivatives, polyvinyl alcohols and their
copolymers, acrylates and methacrylates.
[0329] Gels are applied to or spread on the skin or introduced into
body cavities. Gels are prepared by treating solutions which have
been prepared as described in the case of the injection solutions
with sufficient thickener that a clear material having an
ointment-like consistency results. The thickeners employed are the
thickeners given above.
[0330] Pour-on formulations are poured or sprayed onto limited
areas of the skin, the active compound penetrating the skin and
acting systemically.
[0331] Pour-on formulations are prepared by dissolving, suspending
or emulsifying the active compound in suitable skin-compatible
solvents or solvent mixtures. If appropriate, other auxiliaries
such as colorants, bioabsorption-promoting substances,
antioxidants, light stabilizers, adhesives are added.
[0332] Suitable solvents which are: water, alkanols, glycols,
polyethylene glycols, polypropylene glycols, glycerol, aromatic
alcohols such as benzyl alcohol, phenylethanol, phenoxyethanol,
esters such as ethyl acetate, butyl acetate, benzyl benzoate,
ethers such as alkylene glycol alkyl ethers such as dipropylene
glycol monomethyl ether, diethylene glycol mono-butyl ether,
ketones such as acetone, methyl ethyl ketone, cyclic carbonates
such as propylene carbonate, ethylene carbonate, aromatic and/or
aliphatic hydrocarbons, vegetable or synthetic oils, DMF,
dimethylacetamide, n-alkylpyrrolidones such as methylpyrrolidone,
n-butylpyrrolidone or n-octylpyrrolidone, N-methylpyrrolidone,
2-pyrrolidone, 2,2-dimethyl-4-oxy-methylene-1,3-diox-olane and
glycerol formal.
[0333] Suitable colorants are all colorants permitted for use on
animals and which can be dissolved or suspended.
[0334] Suitable absorption-promoting substances are, for example,
DMSO, spreading oils such as isopropyl myristate, dipropylene
glycol pelargonate, silicone oils and copolymers thereof with
polyethers, fatty acid esters, triglycerides, fatty alcohols.
[0335] Suitable antioxidants are sulfites or metabisulfites such as
potassium metabisulfite, ascorbic acid, butylhydroxytoluene,
butylhydroxyanisole, tocopherol.
[0336] Suitable light stabilizers are, for example, novantisolic
acid.
[0337] Suitable adhesives are, for example, cellulose derivatives,
starch derivatives, polyacrylates, natural polymers such as
alginates, gelatin.
[0338] Emulsions can be administered orally, dermally or as
injections.
[0339] Emulsions are either of the water-in-oil type or of the
oil-in-water type.
[0340] They are prepared by dissolving the active compound either
in the hydrophobic or in the hydrophilic phase and homogenizing
this with the solvent of the other phase with the aid of suitable
emulsifiers and, if appropriate, other auxiliaries such as
colorants, absorption-promoting substances, preservatives,
antioxidants, light stabilizers, viscosity-enhancing
substances.
[0341] Suitable hydrophobic phases (oils) are: liquid paraffins,
silicone oils, natural vegetable oils such as sesame oil, almond
oil, castor oil, synthetic triglycerides such as caprylic/capric
biglyceride, triglyceride mixture with vegetable fatty acids of the
chain length C.sub.8-C.sub.12 or other specially selected natural
fatty acids, partial glyceride mixtures of saturated or unsaturated
fatty acids possibly also containing hydroxyl groups, mono- and
diglycerides of the C.sub.8-C.sub.10 fatty acids, fatty acid esters
such as ethyl stearate, di-n-butyryl adipate, hexyl laurate,
dipropylene glycol perlargonate, esters of a branched fatty acid of
medium chain length with saturated fatty alcohols of chain length
C.sub.16-C.sub.18, isopropyl myristate, isopropyl palmitate,
caprylic/capric acid esters of saturated fatty alcohols of chain
length C.sub.12-C.sub.18, isopropyl stearate, oleyl oleate, decyl
oleate, ethyl oleate, ethyl lactate, waxy fatty acid esters such as
synthetic duck coccygeal gland fat, dibutyl phthalate, diisopropyl
adipate, and ester mixtures related to the latter, fatty alcohols
such as isotridecyl alcohol, 2-octyldodecanol, cetylstearyl
alcohol, oleyl alcohol, and fatty acids such as oleic acid and
mixtures thereof
[0342] Suitable hydrophilic phases are: water, alcohols such as
propylene glycol, glycerol, sorbitol and mixtures thereof
[0343] Suitable emulsifiers are:
non-ionic surfactants, e.g. polyethoxylated castor oil,
polyethoxylated sorbitan monooleate, sorbitan monostearate,
glycerol monostearate, polyoxyethyl stearate, alkylphenol
polyglycol ether; ampholytic surfactants such as di-sodium
N-lauryl-p-iminodipropionate or lecithin; anionic surfactants, such
as sodium lauryl sulfate, fatty alcohol ether sulfates,
mono/dialkyl polyglycol ether orthophosphoric acid ester
monoethanolamine salt; cation-active surfactants, such as
cetyltrimethylammonium chloride.
[0344] Suitable further auxiliaries are: substances which enhance
the viscosity and stabilize the emulsion, such as
carboxymethylcellulose, methylcellulose and other cellulose and
starch derivatives, polyacrylates, alginates, gelatin, gum arabic,
polyvinylpyrrolidone, polyvinyl alcohol, copolymers of methyl vinyl
ether and maleic anhydride, polyethylene glycols, waxes, colloidal
silicic acid or mixtures of the substances mentioned.
[0345] Suspensions can be administered orally or
topically/dermally. They are prepared by suspending the active
compound in a suspending agent, if appropriate with addition of
other auxiliaries such as wetting agents, colorants,
bioabsorption-promoting substances, preservatives, antioxidants,
light stabilizers.
[0346] Liquid suspending agents are all homogeneous solvents and
solvent mixtures.
[0347] Suitable wetting agents (dispersants) are the emulsifiers
given above.
[0348] Other auxiliaries which may be mentioned are those given
above.
[0349] Semi-solid preparations can be administered orally or
topically/dermally. They differ from the suspensions and emulsions
described above only by their higher viscosity.
[0350] For the production of solid preparations, the active
compound is mixed with suitable excipients, if appropriate with
addition of auxiliaries, and brought into the desired form.
[0351] Suitable excipients are all physiologically tolerable solid
inert substances. Those used are inorganic and organic substances.
Inorganic substances are, for example, sodium chloride, carbonates
such as calcium carbonate, hydrogencarbonates, aluminium oxides,
titanium oxide, silicic acids, argillaceous earths, precipitated or
colloidal silica, or phosphates. Organic substances are, for
example, sugar, cellulose, foodstuffs and feeds such as milk
powder, animal meal, grain meals and shreds, starches.
[0352] Suitable auxiliaries are preservatives, antioxidants, and/or
colorants which have been mentioned above.
[0353] Other suitable auxiliaries are lubricants and glidants such
as magnesium stearate, stearic acid, talc, bentonites,
disintegration-promoting substances such as starch or crosslinked
polyvinylpyrrolidone, binders such as starch, gelatin or linear
polyvinylpyrrolidone, and dry binders such as microcrystalline
cellulose.
[0354] In general, "parasiticidally effective amount" means the
amount of active ingredient needed to achieve an observable effect
on growth, including the effects of necrosis, death, retardation,
prevention, and removal, destruction, or otherwise diminishing the
occurrence and activity of the target organism. The parasiticidally
effective amount can vary for the various compounds/compositions
used in the invention. A parasiticidally effective amount of the
compositions will also vary according to the prevailing conditions
such as desired parasiticidal effect and duration, target species,
mode of application, and the like.
[0355] The compositions which can be used in the invention can
comprise generally from about 0.001 to 95 wt % of the active
compounds of the mixtures of the present invention.
[0356] Generally it is favorable to apply the active compounds of
the mixtures of the present invention in total amounts of 0.5 mg/kg
to 100 mg/kg per day, preferably 1 mg/kg to 50 mg/kg per day.
[0357] Ready-to-use preparations contain the active compounds of
the mixtures of the present invention acting against parasites,
preferably ectoparasites, in concentrations of 10 ppm to 80 per
cent by weight, preferably from 0.1 to 65 per cent by weight, more
preferably from 1 to 50 per cent by weight, most preferably from 5
to 40 per cent by weight.
[0358] Preparations which are diluted before use contain the active
compounds of the mixtures of the present invention acting against
ectoparasites in concentrations of 0.5 to 90 per cent by weight,
preferably of 1 to 50 per cent by weight.
[0359] Furthermore, the preparations comprise the active compounds
of the mixtures of the present invention against endoparasites in
concentrations of 10 ppm to 2 per cent by weight, preferably of
0.05 to 0.9 per cent by weight, very particularly preferably of
0.005 to 0.25 per cent by weight.
[0360] In a preferred embodiment of the present invention, the
compositions comprising the mixtures of the present invention are
applied dermally/topically.
[0361] In a further preferred embodiment, the topical application
is conducted in the form of compound-containing shaped articles
such as collars, medallions, ear tags, bands for fixing at body
parts, and adhesive strips and foils.
[0362] Generally it is favorable to apply solid formulations which
release the active compounds of the mixtures of the present
invention in total amounts of 10 mg/kg to 300 mg/kg, preferably 20
mg/kg to 200 mg/kg, most preferably 25 mg/kg to 160 mg/kg body
weight of the treated animal in the course of three weeks.
[0363] For the preparation of the shaped articles, thermoplastic
and flexible plastics as well as elastomers and thermoplastic
elastomers are used. Suitable plastics and elastomers are polyvinyl
resins, polyurethane, polyacrylate, epoxy resins, cellulose,
cellulose derivatives, polyamides and polyester which are
sufficiently compatible with the compounds of formula I. A detailed
list of plastics and elastomers as well as preparation procedures
for the shaped articles is given e.g. in WO 03/086075.
EXAMPLES
[0364] Some of the preferred compound I examples are characterized
by their physical data in the following table C.I.2. The
characterization can be done by coupled High Performance Liquid
Chromatography/mass spectrometry (HPLC/MS), by NMR or by their
melting points.
[0365] The compounds were characterized by .sup.1H-NMR. The signals
are characterized by chemical shift (ppm) vs. tetramethylsilane, by
their multiplicity and by their integral (relative number of
hydrogen atoms given). The following abbreviations are used to
characterize the multiplicity of the signals: M=multiplett,
q=quartett, t=triplett, d=doublet and s=singulett.
[0366] The compounds were also characterized by HPLC/MS. Analytical
HPLC column: RP-18 column Chromolith Speed ROD from Merck KgaA,
Germany). Elution: acetonitrile +0.1% trifluoroacetic acid
(TFA)/water +0.1% trifluoroacetic acid (TFA) in a ratio of from
5:95 to 95:5 in 5 minutes at 40.degree. C.
[0367] Physical data of some specific compound examples of
isoxazoline compounds of formula I:
TABLE-US-00003 TABLE C.I.2 HPLC-MS .sup.1H NMR Compound (t.sub.r =
reten- (in CDCl.sub.3): example Structure of compound I tion time)
.delta. [ppm] C.I.73 ##STR00012## t.sub.r = 3.32 min; m = 494.0
.sup.1H-NMR (500 MHz,CDCl.sub.3): = 8.50 (d, 1H), 7.95 (m, 1H),
7.90 (m, 2H), 7.70 (m, 3H), 7.52 (s, 2H), 7.40 (m, 1H), 7.35 (m,
1H), 7.25 (m, 1H), 4.75 (s, 2H), 4.10 (d, 1H), 3.75 (m, 1H).
C.I.235 ##STR00013## t.sub.r = 3.40 min; m = 508.0 .sup.1H-NMR (500
MHz, CDCl.sub.3): = 8.55 (m, 1H), 7.70 (m, 1H), 7.50 (m, 5H), 7.45
(s, 1H), 7.40 (m, 1H), 7.25 (m, 2H), 4.75 (d, 2H), 4.05 (d, 1H),
3.68 (d, 1H), 2.50 (s, 3H). C.I.240 ##STR00014## t.sub.r = 3.911
min; m = 556.1 .sup.1H-NMR (500 MHz, CDCl.sub.3): = 7.42-7.58 (m,
6H), 7.01 (br dd, 1H), 6.77 (br. dd, 1H), 4.20 (d, 2H), 4.08 (d,
1H), 3.95 (m, 1H), 3.71 (d, 1H), 2.44 (s, 3H). C.I.397 ##STR00015##
t.sub.r = 3.59 min; m = 544.1 .sup.1H-NMR (500 MHz, CDCl.sub.3): =
8.85 (m, 1H), 8.52 (m, 1H), 8.47 (m, 1H), 7.30-7.80 (m, 10H), 7.25
(m, 1H), 4.85 (m, 2H), 4.26 (d, 1H), 3.88 (d, 1H).
Biology
[0368] Synergism can be described as an interaction where the
combined effect of two or more compounds is greater than the sum of
the individual effects of each of the compounds. The presence of a
synergistic effect in terms of percent control, between two mixing
partners (X and Y) can be calculated using the Colby equation
(Colby, S. R., 1967, Calculating Synergistic and Antagonistic
Responses in Herbicide Combinations, Weeds, 15, 20-22):
E = XY 100 ##EQU00001##
[0369] When the observed combined control effect is greater than
the expected combined control effect (E), then the combined effect
is synergistic.
[0370] The following tests can demonstrate the control efficacy of
compounds, mixtures or compositions of this invention on specific
pests. However, the pest control protection afforded by the
compounds, mixtures or compositions is not limited to these
species. In certain instances, combinations of a compound of this
invention with other invertebrate pest control compounds or agents
are found to exhibit synergistic effects against certain important
invertebrate pests.
Test B.1 Control of Green Peach Aphid (Myzus persicae)
[0371] For evaluating control of green peach aphid (Myzus persicae)
through systemic means the test unit consisted of
96-well-microtiter plates containing liquid artificial diet under
an artificial membrane.
[0372] The compounds or mixtures were formulated using a solution
containing 75 wt % water and 25 wt % DMSO. Different concentrations
of formulated compounds or mixtures were pipetted into the aphid
diet, using a custom built pipetter, at two replications. For
experimental mixtures in these tests identical volumes of both
mixing partners at the desired concentrations respectively, were
mixed together.
[0373] After application, 5-8 adult aphids were placed on the
artificial membrane inside the microtiter plate wells. The aphids
were then allowed to suck on the treated aphid diet and incubated
at 23.+-.1.degree. C., 50.+-.5% RH for 3 days. Aphid mortality and
fecundity was then visually assessed. For the mixture tested the
results are listed in table B.1.
TABLE-US-00004 TABLE B.1 Control of Green Peach Aphid (Myzus
persicae) ##STR00016## Test compound is C.I.240: Green Peach Aphid
ppm Average Control % Thiamethoxam + test compound C.I.240 0 + 2 0
0.4 + 0 25 0.4 + 2 100* Imidacloprid + test compound C.I.240 0 +
0.08 0 0.4 + 0 0 0.4 + 0.08 100* *synergistic control effect
according to Colby's equation
Test B.2 Control of Boll Weevil (Anthonomus grandis)
[0374] For evaluating control of boll weevil (Anthonomus grandis)
the test unit consisted of 24-well-microtiter plates containing an
insect diet and 20-30 A. grandis eggs.
[0375] The compounds or mixtures were formulated using a solution
containing 75 wt % water and 25 wt % DMSO. Different concentrations
of formulated compounds or mixtures were sprayed onto the insect
diet at 20 .mu.l, using a custom built micro atomizer, at two
replications.
[0376] For experimental mixtures in these tests identical volumes
of both mixing partners at the desired concentrations respectively,
were mixed together.
[0377] After application, microtiter plates were incubated at
23.+-.1.degree. C., 50.+-.5% RH for 5 days. Egg and larval
mortality was then visually assessed. For the mixture tested the
results are listed in table B.2.
TABLE-US-00005 TABLE B.2 Control of Boll Weevil (Anthonomus
grandis) ##STR00017## Test compound is C.I.240: Boll Weevil ppm
Average Control % Alpha-Cypermethrin + test compound C.I.240 0 +
0.4 50 0.08 + 0 0 0.08 + 0.4 100* Abamectin + test compound C.I.240
0 + 0.08 0 0.016 + 0 50 0.016 + 0.08 100* Flonicamid + test
compound C.I.240 0 + 0.4 50 4 + 0 0 4 + 0.4 100* *synergistic
control effect according to Colby's equation
[0378] In the following further test descriptions are given, which
might also be used in order to evaluate the biological activity of
the mixtures of the invention.
Test B.3
[0379] For evaluating control of vetch aphid (Megoura viciae)
through contact or systemic means the test unit consists of
24-well-microtiter plates containing broad bean leaf disks.
[0380] The compounds or mixtures are formulated using a solution
containing 75 wt % water and 25 wt % DMSO. Different concentrations
of formulated compounds or mixtures are sprayed onto the leaf disks
at 2.5 .mu.l, using a custom built micro atomizer, at two
replications.
[0381] For experimental mixtures in these tests identical volumes
of both mixing partners at the desired concentrations respectively,
are mixed together.
[0382] After application, the leaf disks are air-dried and 5-8
adult aphids are placed on the leaf disks inside the microtiter
plate wells. The aphids are then allowed to suck on the treated
leaf disks and incubated at 23.+-.1.degree. C., 50.+-.5% RH
(relative humidity) for 5 days. Aphid mortality and fecundity is
then visually assessed.
Test B.4
[0383] For evaluating control of Mediterranean fruitfly (Ceratitis
capitata) the test unit consists of 96-well-microtiter plates
containing an insect diet and 50-80 C. capitata eggs.
[0384] The compounds or mixtures are formulated using a solution
containing 75 wt % water and 25 wt % DMSO. Different concentrations
of formulated compounds or mixtures are sprayed onto the insect
diet at 5 .mu.l, using a custom built micro atomizer, at two
replications.
[0385] For experimental mixtures in these tests identical volumes
of both mixing partners at the desired concentrations respectively,
are mixed together.
[0386] After application, microtiter plates are incubated at
28.+-.1.degree. C., 80.+-.5% RH for 5 days. Egg and larval
mortality is visually assessed.
Test B.5
[0387] For evaluating control of tobacco budworm (Heliothis
virescens) the test unit consists of 96-well-microtiter plates
containing an insect diet and 15-25 H. virescens eggs.
[0388] The compounds or mixtures are formulated using a solution
containing 75 wt % water and 25 wt % DMSO. Different concentrations
of formulated compounds or mixtures are sprayed onto the insect
diet at 10 .mu.l, using a custom built micro atomizer, at two
replications.
[0389] For experimental mixtures in these tests identical volumes
of both mixing partners at the desired concentrations respectively,
are mixed together.
[0390] After application, microtiter plates are incubated at
28.+-.1.degree. C., 80.+-.5% RH for 5 days. Egg and larval
mortality is visually assessed.
Test B.6
[0391] For evaluating control of bird cherry aphid (Rhopalosiphum
padi) through contact or systemic means the test unit consists of
96-well-microtiter plates containing barley leaf disks.
[0392] The compounds or mixtures are formulated using a solution
containing 75 wt % water and 25 wt % DMSO. Different concentrations
of formulated compounds or mixtures are sprayed onto the leaf disks
at 2.5 .mu.l, using a custom built micro atomizer, at two
replications.
[0393] For experimental mixtures in these tests identical volumes
of both mixing partners at the desired concentrations respectively,
are mixed together.
[0394] After application, the leaf disks are air-dried and 5-8
adult aphids placed on the leaf disks inside the microtiter plate
wells. The aphids are then allowed to suck on the treated leaf
disks and incubated at 25.+-.1.degree. C., 80.+-.5% RH for 3 to 5
days. Aphid mortality and fecundity is visually assessed.
* * * * *