MXPA06005262A - Combination of active substances with insecticidal properties - Google Patents

Abstract

The invention relates to novel insecticidal combinations of active substances comprising anthrananilic acid amides and other insecticidal active substances from the group of pyrethroids. Said combinations are highly suitable for combatting pests such as insects.

Description

COMBINATIONS OF ACTIVE PRODUCTS WITH INSECTICIDAL PROPERTIES Field of the invention The present invention relates to new combinations of active products, which are constituted by anthranilic acid amides, known, on the one hand and, on the other hand, by known insecticidal active compounds and they are adequate, in a very good way, for the fight against animal pests such as insects. BACKGROUND OF THE INVENTION It is already known that certain anthranilic acid diamides have insecticidal properties (WO 01/70671, WO 02/094791, WO 03/015519, WO 03/016284, WO 03/015518, WO 03/024222, WO 03/016282, WO 03/016283, WO 03/062226, WO 03/027099). Hereby, express reference is made to the formulas and generic definitions as well as to the individual compounds described therein. In addition, it is already known that a large number of heterocycles, organic compounds of tin, benzylureas and pyrethroids have insecticidal and acaricidal properties (see publications WO 93/22297, WO 93/10083, DE-A 26 41 343, EP-A 347 488, EP-A 210 487, US 3,364,177 and EP-A 234 045). Of course, the activity of these products is not always satisfactory either.

REF.:172736 DETAILED DESCRIPTION OF THE INVENTION It has now been found that mixtures formed by anthranilic acid amides of the formula (I) (group 1) wherein A1 and A2 signify, independently of one another, oxygen or sulfur, X1 signifies N or CR10, R1 signifies hydrogen or means alkyl having 1 to 6 carbon atoms, alkenyl having 2 to 6 carbon atoms, alkynyl having 2 to 6 carbon or cycloalkyl atoms with 3 to 6 carbon atoms each substituted, if appropriate, one or more times, the substituents being independently selected from R 6, halogen, cyano, nitro, hydroxy, alkoxy with 1 to 4 atoms of carbon, alkylthio with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, alkoxycarbonyl with 2 to 4 carbon atoms, alkylamino with 1 to 4 carbon atoms, dialkylamino with 2 to 8 carbon atoms, cycloalkylamino with 3 to 6 carbon atoms, (C 1-4 -alkyl) cycloalkylamino with 3 to 6 carbon atoms or R 11, R 2 signifies hydrogen, alkyl with 1 to 6 carbon atoms, alkenyl with 2 a 6 carbon atoms, alkynyl with 2 to 6 carbon atoms, cycloalkyl with 3 to 6 carbon atoms, alkoxy with 1 to 4 carbon atoms, alkylamino with 1 to 4 carbon atoms, dialkylamino with 2 to 8 carbon atoms, cycloalkylamino with 3 to 6 carbon atoms, alkoxycarbonyl with 2 to 6 carbon atoms or alkylcarbonyl with 2 to 6 carbon atoms, R3 means hydrogen, R11 or means alkyl with 1 to 6 carbon atoms, alkenyl with 2 to 6 carbon atoms carbon, alkynyl with 2 to 6 carbon atoms, cycloalkyl with 3 to 6 carbon atoms respectively substituted, if appropriate, one or more times, the substituents being independently selectable from Re, halogen, cyano, nitro, hydroxy alkoxy with 1 to 4 carbon atoms, halogenalkoxy with 1 to 4 carbon atoms, alkylthio with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, alkoxycarbonyl with 2 a 6 atoms of carbon, alkylcarbonyl with 2 to 6 carbon atoms, trialkylsilyl with 3 to 6 carbon atoms, R11, phenyl, phenoxy or a heteroaromatic ring with 5 or 6 members, where each phenyl, phenoxy or heteroaromatic ring may be substituted, if appropriate. with 5 or 6 members and being able to choose the substituents, independently from each other, between one to three residues W or one or more residues R12, or R2 and R3 can be linked together and form the M ring, R4 means hydrogen, alkyl with 1 to 6 carbon atoms, alkenyl with 2 to 6 carbon atoms, alkynyl with 2 to 6 carbon atoms, cycloalkyl with -3 to 6 carbon atoms, halogen-l-alkyl with 1 to 6 carbon atoms, halogenalkenyl with 2 to 6 carbon atoms, halogenalkynyl with 2 to 6 carbon atoms, halogencycloalkyl with 3 to 6 carbon atoms, halogen, cyano, nitro, hydroxy, alkoxy with 1 to 4 carbon atoms, haloalkoxy with 1 to 4 carbon atoms, alkylthio with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, halogenalkylthio with 1 to 4 carbon atoms, halogenoalkylsulfinyl with 1 to 4 carbon atoms, haloalkylsulfonyl with 1 to 4 carbon atoms, alkylamino with 1 to 4 carbon atoms, dialkylamino with 2 to 8 carbon atoms, cycloalkylamino with 3 to 6 carbon atoms, trialkylsilyl with 3 to 6 carbon atoms or means phenyl, benzyl or phenoxy each substituted, if appropriate, one or several times, it being possible to choose the substituents, independently of each other, between alkyl having 1 to 4 carbon atoms, alkenyl having 2 to 4 carbon atoms, alkynyl with 2 to 4 carbon atoms, cycloalkyl with 3 to 6 carbon atoms, halogenal with 1 to 4 carbon atoms, halogenalkenyl with 2 to 4 carbon atoms, halogenalkynyl with 2 to 4 carbon atoms, halogencycloalkyl with 3 to 6 carbon atoms, halogen, cyano, nitro, alkoxy with 1 to 4 carbon atoms, halogenalkoxy with 1 to 4 carbon atoms, alkylthio with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, alkylamino with 1 to 4 carbon atoms, dialkylamino with 2 to 8 carbon atoms, cycloalkylamino with 3 to 6 carbon atoms,(alkyl) cycloalkylamino with 3 to 6 carbon atoms, alkylcarbonyl with 2 to 4 carbon atoms, alkoxycarbonyl with 2 to 6 carbon atoms, alkylarylcarbonyl with 2 to 6 carbon atoms, dialkylaminocarbonyl with 3 to 8 carbon atoms or trialkylsilyl with 3 to 6 carbon atoms R8 respectively mean, independently of one another, hydrogen, halogen or mean alkyl having 1 to 4 carbon atoms, halogen alkyl having 1 to 4 carbon atoms, R12, G, J, -OJ, -OG, -S (0) pJ, -S (0) pG, -S (O) p-phenyl, respectively substituted, the substituents being optionally independently selected from one to three residues W or from R12, alkyl from 1 to 10 carbon atoms, alkenyl with 2 to 6 carbon atoms, alkynyl with 2 to 6 carbon atoms, alkoxy with 1 to 4 carbon atoms or alkylthio with 1 to 4 carbon atoms, each substituent may be substituted independently each other, by one or more substituents chosen two between G, J, Rs, halogen, cyano, nitro, amino, hydroxy, alkoxy with 1 to 4 carbon atoms, halogenalkoxy with 1 to 4 carbon atoms, alkylthio with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, halogenalkylthio with 1 to 4 carbon atoms, halogenoalkylsulfinyl with 1 to 4 carbon atoms, halogenoalkylsulfonyl with 1 to 4 carbon atoms, alkylamino with 1 to 4 carbon atoms, dialkylamino with 2 to 8 carbon atoms, trialkylsilyl having 3 to 6 carbon atoms, phenyl or phenoxy, each phenyl or phenoxy ring may optionally be substituted and substituents may be chosen independently from one to three residues W or one or more radicals R 12, G respectively represent, independently of each other, a carbocyclic or heterocyclic ring, non-aromatic, with 5 or 6 members, containing, if appropriate, one or two ring members selected from the group consisting of group C (= 0), SO or S (= 0) 2, and which may be substituted, if appropriate, by one to four substituents chosen, independently from each other, between alkyl having 1 to 2 carbon atoms, halogen, cyano , nitro or alkoxy with 1 to 2 carbon atoms, or independently, mean alkenyl with 2 to 6 carbon atoms, alkynyl with 2 to 6 carbon atoms, cycloalkyl with 3 to 7 carbon atoms, (cyano) cycloalkyl with 3 to 7 carbon atoms, (C 1 -C 4 -alkyl) C 3 -C 6 -cycloalkyl, (C 3 -C 6 -cycloalkyl) C 1 -C 4 -alkyl, and may be substituted each Cycloalkyl, (alkyl) cycloalkyl and (cycloalkyl) -alkyl, if appropriate, by one or more halogen atoms, J mean respectively, independently of each other, a heteroaromatic ring with 5 or 6 members, optionally substituted, the substituents, independently of each other, between one to three residues W or one or more residues R12, R6 mean, independently of each other, -C (= E1) R19, LC ^ E ^ R19, -C (= E1) LR19, -LC (= E1) LR19, -OP (= Q) (OR19) 2, -S02LR18 or - LS02LR19, meaning each E1, independently of each other, 0, S, N-R15, N-OR15, NN (R15) 2, NS = 0, N-CN or N-N02 , R7 signifies hydrogen, alkyl having 1 to 4 carbon atoms, halogenoalkyl with 1 to 4 carbon atoms, halogen, alkoxy with 1 to 4 carbon atoms, halogenalkoxy with 1 to 4 carbon atoms, alkylthio with 1 to 4 carbon atoms. carbon, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, halogenalkylthio with 1 to 4 carbon atoms, halogenalkylsulfinyl with 1 to 4 carbon atoms, halogenoalkylsulfonyl with 1 to 4 carbon atoms, R9 means haloalkyl with 1 to 4 carbon atoms, haloalkoxy with 1 to 4 carbon atoms, haloalkylsulfinyl with 1 to 4 carbon atoms or halogen, R10 means hydrogen, alkyl with 1 to 4 carbon atoms, haloalkyl with 1 to 4 atoms carbon, halogen, cyano or halogenalkoxy with 1 to 4 carbon atomsR <11> each independently represent alkylthio having 1 to 6 carbon atoms, alkylsulfenyl having 1 to 6 carbon atoms, haloalkylthio with 1 to 6 carbon atoms, halogenoalkylsulfenyl having 1 to 6 carbon atoms, phenylthio or phenylsulfenyl substituted respectively , if necessary, from one to three times, the substituents being independently selectable from the list formed by W, -S (0) nN (R16) 2 / -C (= 0) R13, -L (C = 0) R14, -S (C = 0) LR14, -C (= 0) LR13, S (0) nNR13C (= 0) R13, -S (0) _NR13C (= 0) LR14 or -S (0) nNR13S (0) 2 R14, L mean respectively, independently of each other, O, NR18 or S, R12 mean respectively, independently of each other, -B (OR17) 2, amino, SH, thiocyanate, trialkylsilyloxy with 3 to 8 carbon atoms, alkyl disulfide with 1 to 4 carbon atoms, -SF5, -C (= E) R19, -LC (= E) R19, C (= E) LR19, -LC (= E) LR19, -OP (= Q) (OR19) 2, -S02LR19 or -LS02LR19, Q means O or S, R 13 are respectively, independently of one another, hydrogen or mean alkyl having 1 to 6 carbon atoms, alkenyl having 2 to 6 carbon atoms, alkynyl having 2 to 6 carbon atoms or cycloalkyl having 3 to 6 carbon atoms each substituted, if appropriate, one or more times, the substituents being independently selected from R6, halogen, cyano, nitro, hydroxy, alkoxy with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, alkylamino with 1 to 4 carbon atoms, dialkylamino with 2 to 8 carbon atoms, cycloalkylamino with 3 to 6 carbon atoms carbon or (C1-C4 alkyl) cycloalkylamino with 3 to 6 carbon atoms, mean respectively, independently of each other, alkyl with 1 to 20 carbon atoms, alkenyl with 2 to 20 carbon atoms, alkynyl with 2 to 20 carbon atoms or cycloalkyl with 3 to 6 carbon atoms substituted, if appropriate, one or more times, the substituents being independently selected from R 6, halogen, cyano, nitro, hydroxy, alkoxy with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, alkylamino with 1 to 4 carbon atoms, dialkylamino with 2 to 8 carbon atoms, cycloalkylamino with 3 to 6 carbon atoms or ( alkyl with 1 to 4 carbon atoms) cycloalkylamino with 3 to 6 carbon atoms or means substituted phenyl, optionally substituents being chosen, independently from each other, from one to three residues W or one or more r these R12, R15 mean respectively, independently of each other, hydrogen or halogenalkyl with 1 to 6 carbon atoms or alkyl with 1 to 6 carbon atoms respectively substituted, if appropriate, once or several times, substituents may be chosen, independently from each other yes, between cyano, nitro, hydroxy, alkoxy with 1 to 4 carbon atoms, halogenalkoxy with 1 to 4 carbon atoms, alkylthio with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, halogenalkylthio with 1 to 4 carbon atoms, halogenalkylsulfinyl with 1 to 4 carbon atoms, halogenalkylsulfonyl with 1 to 4 carbon atoms, alkylamino with 1 to 4 carbon atoms, dialkylamino with 2 to 8 carbon atoms, alkoxycarbonyl with 2 to 6 carbon atoms, alkylcarbonyl with 2 to 6 carbon atoms, trialkylsilyl with 3 to 6 carbon atoms or phenyl, optionally substituted, it being possible to choose the substituents, independently of one another, between one to three residues W or one or more radicals R12, or N (R15) 2 means a ring, which forms the ring M, R16 means alkyl with 1 to 12 carbon atoms or halogenalkyl with 1 to 12 carbon atoms, or N (R16) 2, means a ring, which forms the ring M, R17 respectively mean, independently of each other, hydrogen or alkyl having 1 to 4 carbon atoms, or B (OR17) 2 means a ring , in which both oxygen atoms are linked through a chain with two to three carbon atoms, which may be substituted, if appropriate, by one or two substituents chosen, independently from each other, between methyl or alkoxycarbonyl with 2 to 6 carbon atoms, R18 respectively mean, independently of one another, hydrogen, alkyl having 1 to 6 carbon atoms or halogenalkyl having 1 to 6 carbon atoms, or N (R13) (R18) means a cycle, which forms the M ring, R19 respectively denotes, independently of one another, hydrogen or means alkyl having from 1 to 6 carbon atoms substituted, if appropriate, one or more times, the substituents being independently selectable from cyano, nitro, hydroxy, alkoxy with 1 to 4 carbon atoms, halogenalkoxy with 1 to 4 carbon atoms, alkylthio with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, halogenalkylthio with 1 to 4 carbon atoms , halogenalkylsulfinyl with 1 to 4 carbon atoms, halogenalkylsulfonyl with 1 to 4 carbon atoms, alkylamino with 1 to 4 carbon atoms, dialkylamino with 2 to 8 carbon atoms, C0H, alkoxycarbonyl with 2 to 6 carbon atoms, alkylcarbonyl with 2 to 6 carbon atoms, trialkylsilyl having 3 to 6 carbon atoms or phenyl, optionally substituted, it being possible to choose the substituents, independently from each other, between not three residues W, halogenalkyl with 1 to 6 carbon atoms, cycloalkyl with 3 to 6 carbon atoms or phenyl or pyridyl respectively substituted, if appropriate, one to three times per W, M means a substituted ring respectively, in case given, from one to four times, containing, in addition to the nitrogen atom, with which the pair of substituents R13 and R18, (R15) 2 or (R? e) 2, of two to 6 carbon atoms and optionally, furthermore, another nitrogen, sulfur or oxygen atom and the substituents may be chosen, independently from each other, between alkyl having 1 to 2 carbon atoms, halogen, cyano, nitro or alkoxy with 1 to 2 carbon atoms. carbon, W mean respectively, independently of each other, alkyl with 1 to 4 carbon atoms, alkenyl with 2 to 4 carbon atoms, alkynyl with 2 to 4 carbon atoms, cycloalkyl with 3 to 6 carbon atoms, haloalkyl with 1 to 4 carbon atoms, halogenalkenyl with 2 to 4 carbon atoms, halogenalkynyl with 2 to 4 carbon atoms, halogencycloalkyl with 3 to 6 carbon atoms, halogen, cyano, nitro, alkoxy with 1 to 4 carbon atoms, halogenalkoxy with 1 to 4 carbon atoms, alkylthio with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, alkylamino with 1 to 4 carbon atoms, dialkylamino with 2 to 8 carbon atoms, cycloalkylamino with 3 to 6 carbon atoms, (C 1 -C 4 -alkyl) C 3 -C 6 -cycloalkylamino, C 2 -C 4 -alkylcarbonyl, C 2 -C 6 -alkoxycarbonyl, C02H, C 2 -C 6 -alkylaminocarbonyl, dialkylaminocarbonyl with 3 to 8 carbon atoms or trialkylsilyl having 3 to 6 carbon atoms, n mean respectively, independently of each other, 0 or 1, p mean respectively, independently of each other, 0, 1 or 2, being present, in the case where ue (a) R5 means hydrogen, alkyl having 1 to 6 carbon atoms, halogenoalkyl with 1 to 6 carbon atoms, halogenoalkenyl with 2 to 6 carbon atoms, halogenoalkynyl with 2 to 6 carbon atoms, halogenoalkoxy with 1 to 4 atoms of carbon, halogenalkylthio with 1 to 4 carbon atoms or halogen and (b) R8 means hydrogen, alkyl with 1 to 6 carbon atoms, halogenalkyl with 1 to 6 carbon atoms, halogenalkenyl with 2 to 6 carbon atoms, haloalkynyl with 2 to 6 carbon atoms, halogenalkoxy with 1 to 4 carbon atoms, halogenalkylthio with 1 to 4 carbon atoms, halogen, alkylcarbonyl with 2 to 4 carbon atoms, alkoxycarbonyl with 2 to 6 carbon atoms, alkylaminocarbonyl with 2 to 6 carbon atoms or dialkylaminocarbonyl with 3 to 8 carbon atoms, (c) at least one substituent, chosen from R6, R11 and R12 and (d), when R12 is not present, at least one R6 or R11 is different from alkylcarbonyl with 2 to 6 carbon atoms, alkoxycarbonyl with 2 to 6 carbon atoms, alkylaminocarbonyl with 2 to 6 carbon atoms and dialkylaminocarbonyl with 3 to 8 carbon atoms and the compounds of the general formula (I), they also include the N-oxides and salts, and at least one active product of the group of pyrethroids (active products of group 2) have synergistic activity and are suitable for the control of animal pests. The compounds of the formula (I) can also be present, depending on the type of the substituents, as isomers or mixtures of geometric and / or optical isomers, with a variable composition, which can be separated, if appropriate, in a customary manner. . Both the pure isomers, as well as the mixtures of the isomers, their preparation and use, as well as the agents that contain them, constitute the object of the present invention. However, the compounds of the formula (I) will be discussed below, even if the pure compounds as well as the mixtures with variable proportions of the isomeric compounds are to be indicated. Preference is given to combinations of active compounds, which contain compounds of the formula (1-1) wherein R2 means hydrogen or alkyl having 1 to 6 carbon atoms, R3 means alkyl having 1 to 6 carbon atoms, which is, if appropriate, substituted by R6, R4 means alkyl having 1 to 4 carbon atoms, haloalkyl with 1 to 2 carbon atoms, halogenalkoxy with 1 to 2 carbon atoms or halogen, R 5 is hydrogen, alkyl having 1 to 4 carbon atoms, halogen with 1 to 2 carbon atoms, halogen with 1 to 2 carbon atoms or halogen, R6 means -C (= E2) R19, -LC (= E2) R19, -C (= E2) LR19 or -LC (= E2) LR19, meaning each E2, independently of each other 0, S, N-R15, N -OR15, NN (R15) 2, and meaning each L, independently of each other, O or NR18, R7 means haloalkyl with 1 to 4 carbon atoms or halogen, R9 means haloalkyl with 1 to 2 carbon atoms, haloalkoxy with 1 to 2 carbon atoms, S (0) p ~ halogenalkyl with 1 to 2 carbon atoms or halogen, R15 signifies, independently of one another, hydrogen or, for example, halogenalkyl having 1 to 6 carbon atoms or alkyl having 1 to 6 carbon atoms substituted, optionally, the substituents being independently selected from cyano, alkoxy with 1 to 4 carbon atoms, halogenalkoxy with 1 to 4 carbon atoms, alkylthio with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, alkylthio with 1 to 4 carbon atoms , halogenalkylsulfinyl with 1 to 4 carbon atoms or halogenalkylsulfonyl with 1 to 4 carbon atoms, R18 respectively mean hydrogen or alkyl with 1 to 4 carbon atoms, R19, respectively, independently of one another, hydrogen or alkyl with 16 carbon atoms, p mean, independently of each other, 0.1, 2. In the definitions mentioned above as preferred, halogen means fluorine, chlorine , bromine and iodine, especially means fluorine, chlorine and bromine. Particularly preferred are combinations of active compounds, which contain compounds of the formula (I-1), in which R 2 is hydrogen or methyl, R 3 is alkyl with 1 to 4 carbon atoms (especially methyl, ethyl, n-, iso-propyl, n-, iso-, sec-, tere.-butyl), R4 means methyl, trifluoromethyl, trifluoromethoxy, fluorine, chlorine, bromine or iodine, R5 means hydrogen, fluorine, chlorine, bromine, iodine, trifluoromethyl or trifluoromethoxy, R7 means chlorine or bromine, R9 means trifluoromethyl, chlorine, bromine, difluoromethoxy or trifluoroethoxy. Particularly preferred are the active compound combinations, which contain the following compounds of the formula (1-1): Example R2 R3 R4 RS R7 R5 Pf. (° C) Nr. 1-1-1 H Me Me Cl Cl CF3 185-186 1-1-2 H Me Me Cl Cl OCH2CF3 207-208 1-1-3 H Me Cl Cl Cl 225-226 1-1-4 H Me Me Cl Cl Br 162-164 1-1-5 H Cl Cl Cl CF3 155-157 1-1- 6 H Cl Cl Cl OCH2CF3 192-195 1-1-7 H Cl Cl CL Cl 205-206 1-1-8 H Me Cl Cl Cl Br 245-246 1-1-9 H i- Me Cl Cl CF3 195-196 Pr 1-1-10 H i- Me Cl Cl OCH2CF3 217-218 Pr 1-1-11 H i- Me Cl Cl Cl 173-175 Pr 1- 1-12 H i- Me Cl Cl Br 159-161 Pr 1-1-13 H i Cl Cl Cl CF 200-201 Pr Example R5 R5 R R5 R7 R5 Pf. (° C) Nr. 1-1-14 H? ^ C? Cl C? OCH2CF3 232-235 Pr 1-1-15 H i Cl Cl Cl Cl 197-199 Pr 1-1-16 H i Cl Cl Cl 188-190 Pr 1-1-17 H Et Me Cl Cl CF3 163- 164 1-1-18 H Et Me Cl Cl 0CH2CF3 205-207 1-1-19 H Et Me Cl Cl Cl 199-200 1-1-20 H Et Me Cl Cl Br 194-195 1-1-21 H Et Cl Cl Cl CF3 201-202 1-1-22 H Et Cl Cl Cl Cl 206-208 1-1-23 H Et Cl Cl Cl Br 214-215 1-1-24 H t- Me Cl Cl CF3 223-225 Bu 1-1-25 H t- Me Cl-Cl Cl 163-165 Bu 1-1-26 H t- Me Cl Cl Br 159-161 Bu 1 -1-27 H t- Cl Cl Cl CF3 170-172 Bu Example RR 'Pf. (° C) Nr. 1-1-28 H t Cl Cl C Cl 172-173 Bu 1-1-29 H t Cl Cl Cl 179-180 Bu 1-1-30 H Me Me Br Cl CF3 222-223 1-1-31 H Et Me Br Cl CF3 192-193 1-1-32 H i- Me Br Cl CF3 197-198 Pr 1-1-33 H t- Me Br Cl CF3 247-248 Bu 1-1-34 H Me Me Br Cl Cl 140-141 1-1-35 H Et Me Br Cl Cl 192-194 1-1-36 H i- Me Br Cl Cl 152-153 Pr 1-1-37 H t- Me Cl Cl Cl 224-225 Bu 1-1-38 H Me Me Br Cl Br 147-149 1-1-39 H Et Me Br Cl Br 194-196 1-1-40 H i- Me Br Cl Br 185-187 Pr 1-1-41 H t- Me Br Cl Br 215-221 Bu Example R2 R3 R3 R5 R7 R5 Pf. (° C) Nr. 1-1-42 H Me Me? C? CF¡ 199-200 1-1-43 H Et Me I Cl CF3 199-200 1-1-44 H i- Me I Cl CF3 188-189 Pr 1-1-45 H t- Me I Cl CF3 242-243 Bu 1-1-46 H Me Me Cl Cl 233-234 1-1-47 H Et Me I Cl Cl 196-197 1-1-48 H i- Me I Cl Cl 189-190 Pr 1-1-49 H t- Me Cl Cl 228-229 Bu 1-1-50 H Me Me I Cl Br 229-230 1-1-51 H iPr Me I Cl Br 191-192 1-1-52 H Me Br Br Cl CF3 162-163 1-1-53 H Et Br Br Cl CF3 188-189 1-1-54 H i- Br Br Cl CF3 192-193 Pr 1-1-55 H t- Br Br Cl CF3 246-247 Bu 1-1-56 H Me Br Br Cl Cl 188-190 1-1-57 H Et Br Br Cl Cl 192-194 Example R R5 R3 R5 R7 R5 Pf. (° C) Nr. 1-1-58 H i- Br Br Cl Cl 197-199 Pr 1-1-59 H t Br Br Cl Cl 210-212 Bu 1-1-60 H Br Br Br Cl 166-168 1-1-61 H Et Br Br Cl Br 196-197 1-1-62 H i- Br Br Cl Br 162-163 Pr 1-1-63 H t- Br Br Cl Br 194-196 Bu 1-1-64 H t- Cl Br Cl CF3 143-145 Bu 1- 1-65 Me Me Br Br Cl Cl 153-155 1-1-66 Me Me Me Br Cl CF3 207-208 1-1-67 Me Me Cl Cl Cl Cl 231-232 1-1-68 Me Me Br Br Cl Br 189-190 1-1-69 Me Me Cl Cl Cl Br 216-218 1-1-70 Me Me Cl Cl Cl CF3 225-227 1-1-71 Me Me Br Br Cl CF3 228-229 1-1-72 H i- Me H Cl CF3 237-239 Pr Combinations of active ingredients are particularly preferred. containing a compound of the following formulas (1-1-21) (1-1-22) (1-1-23) (1-1-24) (1-1-26) (1-1-27) (1-1-32) (1-1-2) 1-1-33) (I-1-3Í (Il-39¡ (1-1-40) (1-1-42) (1-1-51) (1-1-52) .1-1- 53) (1-1-54) (1-1-55; (1-1-56) (1-1-71) (1-1-72) Pyrethroids are known active compounds with insecticidal and acaricidal properties, In accordance with the invention, combinations of active products, preferably containing the following pyrethroids (active group 2): (2-1) Acrinathrin (known from EP-A 0 048) will be preferred. 186) and / or (2-2) Alpha-cypermethrin (known from EP-A 0 067 461) and / or (2-3) Betacyfluthrin (known from EP-A 0 206 149) and / or (2-4) Cyhalothrin (known by the publication DE-A 28 02 962) and / or (2-5) Cypermethrin (known from the publication DE-A-2 326 077) and / or (2-6) Deltamethrin (known from the publication DE-A 23 26 077) reported by the publication DE-A 27 Occurred by publication DE-A 31 17 and / or (2-9) Fenpropathrin (known by the publication DE-A 22 31 312) and / or (2-10) Fenvalerat (known by the publication DE-A 23 35 347) i and / or (2-11) Flucythrinat (known for the publication DE-A 27 57 066) and / or (2-12) Lambda-Cyhalothrin (known as EP-A 0 106 469) and / or (2-13) Permethrin (known from the publication DE-A 23 26 077) and / or (2-14) Taufluvalinat (known by the publication EP-A 0 038 617) and / or (2-15) Tralomethrin (known from the publication DE-A 27 42 546) and / or (2-16) Zeta-cypermethrin (known from EP-A 0 026 542) and / or (2-17) Cyfluthrin (known from the publication DE-A 27 09 264) and / or (2-18) Bifenthrin (known by the publication EP-A 0 049 977) and / or (2-19) Cycloprothrin (known from the publication DE-A 26 53 189) and / or (2-20) Eflusilanat (known from the publication, DE-A 36 04 781) by the publication DE-A 37 08 (2-22) Pyrethrin (known from The Pesticide Manual, 1997, 11th edition, page 1056) R2i = -CH = CH. or -CH3 or -CH2CH3 and / or (2-23) Resmethrin (known from GB-A 1 168 797) and / or (2-24) Gamma-Cyhalothrin (known from GB-A 2 143 823) Particularly preferably, the active compound combinations according to the invention contain at least one pyrethroid of group 2 chosen from (2-1) Acrinathrin (2-3) Betacyfluthrin. (2-5) Cypermethrin. (2-6) Deltamethrin. '(2-12) Lambda-Cyhalothrin. (2-14) Taufluvalinat. (2-24) Gamma-Cyhalothrin. Combinations of active products are especially preferred., containing the compound of the formula (1-1-9) as well as a pyrethroid of group 2, chosen from the compounds (2-1) to (2-24). Particularly preferred are the active compound combinations, which contain the compound of the formula (1-1-11) as well as a pyrethroid of group 2, selected from among the compounds (2-1) to (2-24). Especially preferred are the active compound combinations, which contain the compound of the formula (1-1-12) as well as a pyrethroid of the group 2, selected from the compounds (2-1) to (2-24). The active compound combinations, mentioned below individually (binary mixtures), which contain a compound of the formula (1-1) and pyrethroid of group 2, should be mentioned: Product combination Product combination Nr. Active Nr., Which contains assets, which contains 3f) (1-1-3) and (2-14) 30f (1-1-42) and (2-14) Taufluvalinat) Taufluvalinat (1-1-3) and (2-24) Gamma- 30g (1-1-42) and (2-24) Gamma- 3g) Cyhalothrin) Cyhalothrin (1-1-4) and (2- 1) 31a (1-1-43) and (2-1) 4a) Acrinathrin) Acrinathrin (1-1-4) and (2-3) 31b (1-1-43) and (2-3) 4b) Betacyfluthrin) Betacyfluthrin (1-1-4) and (2-5) 31c (1-1-43) and (2-5) 4c) Cypermethrin Cypermethrin (1-1-4) and (2-6) 31d (1-1-43) and (2-6) 4d) Deltamethrin Deltamethrin (1-1-4) and (2-12) Lambda- 31e (1-1-43) and (2-12) 4e) Cyhalothrin) Lambda-Cyhalothrin (1-1-4) and (2-14) 31f (1-1-43) and (2-14) 4f) Taufluvalinat) Taufluvalinat (1-1-4) and (2-24) Gamma- 31g (1-1-43) and (2-24) Gamma- 4g) Cyhalothrin) Cyhalothrin d-1-5) and (2) -1) 32a (1-1-44) and (2-1) 5a) Acrinathrin) Acrinathrin (1-1-5). and (2-3) 32b (1-1-44) and (2-3) 5b) Betacyfluthrin) Betacyfluthrin Product combination - Product combination Nr. Active Nr., Which contains assets, which contains 5c) d-1-5) and (2-5) 32c (1-1-44) and (2-5) Cypermethrin) Cypermethrin (1-1-5) and (2-6) 32d (1-1-44) and (2-6) 5d) Deltamethrin -) Deltamethrin (1-1-5) and (2-12) The bda- 32e (1-1-44) and (2-12) 5e) Cyhalothrin) Lambda-Cyhalothrin (1-1-5) and (2-14) 32f (1-1-44) and (2-14) 5f) Taufluvalinat) Taufluvalinat (1-1-5) and (2-24) Gamma- 32g (1-1-44) and (2-24) Gamma- 5g) Cyhalothrin) Cyhalothrin (1-1-6) and ( 2-1) 33a (1-1-50) and (2-1) 6a) Acrinathrin) Acrinathrin (1-1-6) and (2-3) 33b (1-1-50) and (2-3) 6b) Betacyfluthrin) Betacyfluthrin (1-1-6) and (2-5) 33c (1-1-50) and (2-5) 6c) Cypermethrin) Cypermethrin (1-1-6) and (2-6) 33d (1-1-50) and (2-6) 6d) Deltamethrin) Deltamethrin (1-1-6) and (2-12) Lambda- 33e (1-1-50) and (2-12) 6e) Cyhaiothrin) Lambda-Cyhalothrin (1-1-6) and (2-14) 33f (1-1-50) and (2-14) 6f) Taufluvalinat) Taufluvalinat Combination of products Combination of products Nr. Active Nr., Which contains assets, which contains 6g) (1-1-6) and (2-24) Gamma- 33g (1-1-50) and (2-24) Gamma- Cyhalothrin) Cyhalothrin (1-1-7) and (2-1) 34a (1-1-51) and (2-1) 7a) Acrinathrin) Acrinathrin (1-1-7) and (2-3) 34b (1-1-51) and (2-3) 7b) Betacyfluthrin) Betacyfluthrin d-1-7) and (2-5) 34c (1-1-51) and (2-5) 7c) Cypermethrin) Cypermethrin d-1-7) and (2-6) 34d (1-1-51) and (2-6) 7d) Deltamethrin > Deltamethrin (1-1-7) and (2-12) Lambda- 34e (1-1-51) and (2-12) 7e) Cyhalothrin) Lambda-Cyhalothrin (1-1-7) and (2-14) 34f (1-1-51) and (2-14) 7f) Taufluvalinat) Taufluvalinat (1-1-7) and (2-24) Gamma- 34g (1-1-51) and (2-24) Gamma- 7g) Cyhalothrin) Cyhalothrin (1-1-8) y ( 2-1) 35a (1-1-52) and (2-1) 8a) Acrinathrin) Acrinathrin (1-1-8) and (2-3) 35b (1-1-52) and (2-3) 8b) Betacyfluthrin) Betacyfluthrin (1-1-8) and (2-5) 35c (1-1-52) and (2-5) 8c) Cypermethrin) Cypermethrin Product combination Product combination Nr. Active Nr., Which contains assets, which contains 8d) (1-1-8) and (2-6) 35d (1-1-52) and (2-6) Deltamethrin) Deltamethrin (1-1-8) and (2-12) Lambda- 35e (1-1-52) and (2-12) 8e) Cyhalothrin) Lambda-Cyhalothrin (1-1-8) and (2-14) 35f (1-1-52) and (2-14) 8f) Taufluvalinat) Taufluvalinat (1-1-8) and (2-24) Gamma- 35g (1-1-52) and (2-24) Gamma- 8g) Cyhalothrin) Cyhalothrin (1-1-9) and ( 2-1) 36a (1-1-53) and (2-1) 9a) Acrinathrin) Acrinathrin (1-1-9) and (2-3) 36b (1-1-53) and (2-3) 9b) Betacyfluthrin) Betacyfluthrin (1-1-9) and (2-5) 36c (1-1-53) and (2-5) 9c) Cypermethrin) Cypermethrin (1-1-9) and (2-6) 36d (1-1-53) and (2-6) 9d) Deltamethrin) Deltamethrin (1-1-9) and (2-12) Lambda- 36e (1-1-53) and (2-12) 9e) Cyhalothrin) Lambda-Cyhalothrin (1-1-9) and (2-14) 36f (1-1-53) and (2-14) 9f) Taufluvalinat) Taufluvalinat (1-1-9) and (2-24) Gamma- 36g (1-1-53) and (2-24) Gamma- 9g) Cyhalothrin) Cyhalothrin Combination of products Combination of products Nr. Active Nr., Which contains assets, which contains 10a (1-1-11) and (2-1) 37a (1-1-54) and (2-1) Acrinathrin) Acrinathrin 10b (1-1-11) and (2-3) 37b (1-1-54) and (2-3) ) Betacyfluthrin) Betacyfluthrin 10c (1-1-11) and (2-5) 37c (1-1-54) and (2-5) ) Cypermethrin) Cypermethrin lOd (1-1-11) and (2-6) 37d (1-1-54) and (2-6) Deltamethrin) Deltamethrin lOe (1-1-11) and (2-12) 37e (1-1-54) and (2-12) ) Lambda-Cyhalothrin) Lambda-Cyhalothrin lOf (1-1-11) and (2-14) 37f (1-1-54) and (2-14) ) Taufluvalinat) Taufluvalinat lOg (1-1-11) and (2-24) Gamma- 37g (1-1-54) -y (2-24) Gamma-) Cyhalothrin) Cyhalothrin lia (1-1-12) and (2-1) 38a (1-1-55) and (2-1) Acrinathrin) Acrinathrin llb (1-1-12) and (2-3) 38b (1-1-55) and (2-3) Betacyfluthrin) Betacyfluthrin 11c (1-1-12) and (2-5) 38c (1-1-55) and (2-5) ) Cypermethrin) Cypermethrin lid (1-1-12) and (2-6) 38d (1-1-55) and (2-6) ) Deltamethrin) Deltamethrin Product combination 1 Product combination Nr. Active Nr., Which contains assets, containing lie (1-1-12) and (2-12) | 38e (1-1-55) and (2-12) ) Lambda-Cyhalothrin) Lambda-Cyhalothrin llf (1-1-12) and (2-14) 38f (1-1-55) and (2-14) Taufluvalinat) Taufluvalinat llg (1-1-12) and (2-24) Gamma- 38g (1-1-55) and (2-24) Gamma-) Cyhalothrin) Cyhalothrin 12a (1-1-13) y ( 2-1) 39a (1-1-56) and (2-1) Acrinathrin) Acrinathrin 12b (1-1-13) and (2-3) 39b (1-1-56) and (2-3) Betacyfluthrin) Betacyfluthrin 12c (1-1-13) and (2-5) 39c (1-1-56) and (2-5) ) Cypermethrin) Cypermethrin 12d (1-1-13) and (2-6) 39d (1-1-56) and (2-6) Deltamethrin) Deltamethrin 12e (1-1-13) and (2-12.) 39e (1-1-56) and (2-12) ) Lambda-Cyhalothrin) Lambda-Cyhalothrin 12f (1-1-13) and (2-14) 39f (1-1-56) and (2-14) Taufluvalinat) Taufluvalinat 12g (1-1-13) and (2-24) Gamma- 39g (1-1-56) and (2-24) Gamma-) Cyhalothrin Cyhalothrin »13a (1-1-15) and ( 2-1) 40a (1-1-57) and (2-1) Acrinathrin) Acrinathrin Combination of products Combination of products Nr. Active Nr., Which contains assets, which contains 13b (1-1-15) and (2-3) 40b (1-1-57) and (2-3) Betacyfluthrin) Betacyfluthrin 13c (1-1-15) and (2-5) 40c (1-1-57) and (2-5) ) Cypermethrin) Cypermethrin 13d (1-1-15) and (2-6) 40d (1-1-57) and (2-6) Deltamethrin) Deltamethrin 13e (1-1-15) and (2-12) 40e (1-1-57) and (2-12) ) Lambda-Cyhalothrin) Lambda-Cyhalothrin 13f (1-1-15) and (2-14) 40f (1-1-57) and (2-14) ) Taufluvalinat) Taufluvalinat 13g (1-1-15) and (2-24) Gamma- 40g (1-1-57) and (2-24) Gamma- Cyhalothrin) Cyhalothrin 14a (1-1-16) and (2-1) 41a (1-1-58) and (2-1) Acrinathrin) Acrinathrin 14b (1-1-16) and (2-3) 41b d-1-58) and (2-3) Betacyfluthrin) Betacyfluthrin 14c (1-1-16) and (2-5) 41c (1-1-58) and (2-5) ) Cypermethrin) Cypermethrin 14d (1-1-16) and (2-6) 41d (1-1-58) and (2-6) Deltamethrin) Deltamethrin 14e (1-1-16) and (2-12) 41e (1-1-58) and (2-12) ) Lambda-Cyhalothrin) Lambda-Cyhalothrin Product combination Product combination Nr. Active Nr., Which contains assets, which contains 14f (1-1-16) and (2-14) 141f (1-1-58) and (2-14) Taufluvalinat) Taufluvalinat 14g (1-1-16) and (2-24) Gamma- 41g (1-1-58) and (2-24) Gamma-) Cyhalothrin > Cyhalothrin 15a (1-1-19) and (2-1) 42a (1-1-60) and (2-1) Acrinathrin) Acrinathrin 15b (1-1-19) and (2-3) 42b (1-1-60) and (2-3) Betacyfluthrin) Betacyfluthrin 15c (1-1-19) and (2-5) 42c (1-1-60) and (2-5) ) Cypermethrin) Cypermethrin 15d (1-1-19) and (2-6) 42d (1-1-60) and (2-6) Deltamethrin) Deltamethrin 15e (1-1-19) and (2-12) 42e (1-1-60) and (2-12) ) Lambda-Cyhalothrin) Lambda-Cyhalothrin 15f (1-1-19) and (2-14) 42f (1-1-60) and (2-14) Taufluvalinat) Taufluvalinat 15g (1-1-19) and (2-24) Gamma- 42g (1-1-60) and (2-24) Gamma-) Cyhalothrin) Cyhalothrin 16a (1-1-21) and ( 2-1) 43a (1-1-61) and (2-1) Acrinathrin > Acrinathrin 16b (1-1-21) and (2-3) 43b (1-1-61) and (2-3) ) Betacyfluthrin) Betacyfluthrin Product combination Product combination Nr. Active Nr., Which contains assets, which contains 16c (1-1-21) and (2-5) 43c (1-1-61) and (2-5) ) Cypermethrin) Cypermethrin 16d (1-1-21) and (2-6) 43d (1-1-61) and (2-6) Deltamethrin) Deltamethrin 16e (1-1-21) and (2-12) 43e (1-1-61) and (2-12) ) Lambda-Cyhalothrin) Lambda-Cyhalothrin 16f (1-1-21) and (2-14) 43f (1-1-61) and (2-14) Taufluvalinat) Taufluvalinat 16g (1-1-21) and (2-24) Gamma- 43g (1-1-61) and (2-24) Gamma-) Cyhalothrin) Cyhalothrin 17a (1-1-22) and ( 2-1) 44a (1-1-62) and (2-1) Acrinathrin) Acrinathrin 17b (1-1-22) and (2-3) 44b (1-1-62) and (2-3) Betacyfluthrin) Betacyfluthrin 17c (1-1-22) and (2-5) 44c (1-1-62) and (2-5) ) Cypermethrin) Cypermethrin 17d (1-1-22) and (2-6) 44d (1-1-62) and (2-6) Deltamethrin) Deltamethrin 17e (1-1-22) and (2-12) 44e (1-1-62) and (2-12) ) Lambda-Cyhalothrin) Lambda-Cyhalothrin 17f (1-1-22) and (2-14) 44f (1-1-62) and (2-14) ) Taufluvalinat) Taufluvalinat Product combination Product combination Nr. Active Nr., Which contains assets, which contains I7g (1-1-22) and (2-24) Gamma- 44g (1-1-62) and (2-24) Gamma-) Cyhalothrin) Cyhalothrin 18a (1-1-23) and (2-1) 45a (1-1-64) and (2-1) Acrinathrin) Acrinathrin 18b (1-1-23) and (2-3) 45b (1-1-64) and (2-3) Betacyfluthrin) Betacyfluthrin 18c (1-1-23) and (2-5) 45c (1-1-64) and (2-5) ) Cypermethrin) Cypermethrin 18d (1-1-23) and (2-6) 45d (1-1-64) and (2-6) Deltamethrin) Deltamethrin 18e (1-1-23) and (2-12) 45e (1-1-64) and (2-12) ) Lambda-Cyhalothrin) Lambda-Cyhalothrin 18f (1-1-23) and (2-14) 45f (1-1-64) and (2-14) Taufluvalinat) Taufluvalinat 18g (1-1-23) and (2-24) Gamma- 45g (1-1-64) and (2-24) Gamma-) Cyhalothrin) Cyhalothrin 19a (1-1-24) y ( 2-1) 46a (1-1-65) and (2-1) Acrinathrin) Acrinathrin 19b (1-1-24) and (2-3) 46b (1-1-65) and (2-3) Betacyfluthrin) Betacyfluthrin 19c (1-1-24) and (2-5) 46c (1-1-65) and (2-5) ) Cypermethrin) Cypermethrin Combination of products Combination of products Nr. Active Nr., Which contains assets, which contains 19d (1-1-24) and (2-6) 46d (1-1-65) and (2-6) Deltamethrin) Deltamethrin 19e (1-1-24) and (2-12) 46e (1-1-65) and (2-12) ) Lambda-Cyhalothrin) Lambda-Cyhalothrin 19f (1-1-24) and (2-14) 46f (1-1-65) and (2-14) ) Taufluvalinat) Taufluvalinat 19g (1-1-24) and (2-24) Gamma- 46g (1-1-65) and (2-24) Gamma- Cyhalothrin) Cyhalothrin 20a (1-1-26) and (2-1) 47a (1-1-66) and (2-1) Acrinathrin) Acrinathrin 20b (1-1-26) and (2-3) 47b (1-1-66) and (2-3) Betacyfluthrin) Betacyfluthrin 20c (1-1-26) and (2-5) 47c (1-1-66) and (2-5) ) Cypermethrin) Cypermethrin 20d (1-1-26) and (2-6) 47d (1-1-66) and (2-6) Deltamethrin) Deltamethrin 20e (1-1-26) and (2-12) 47e (1-1-66) and (2-12) ) Lambda-Cyhalothrin Lambda-Cyhalothrin > 20f (1-1-26) and (2-14) 47f (1-1-66) and (2-14) ) Taufluvalinat) Taufluvalinat 20g (1-1-26) and (2-24) Gamma- 47g (1-1-66) and (2-24) Gamma- ) Cyhalothrin) Cyhalothrin Product combination Product combination Nr. Active Nr., Which contains assets, which contains 21a (1-1-27) and (2-1) 48a (1-1-67) and (2-1) Acrinathrin) Acrinathrin 21b (1-1-27) and (2-3) 48b (1-1-67) and (2-3) Betacyfluthrin) Betacyfluthrin 21c (1-1-27) and (2-5) 48c (1-1-67) and (2-5) ) Cypermethrin) Cypermethrin 21d (1-1-27) and (2-6) 48d (1-1-67) and (2-6) Deltamethrin) Deltamethrin 21e (1-1-27) and (2-12) 48e (1-1-67) and (2-12) ) Lambda-Cyhalothrin) Lambda-Cyhalothrin 21f (1-1-27) and (2-14) 48f (1-1-67) and (2-14) Taufluvalinat) Taufluvalinat 21g (1-1-27) and (2-24) Gamma- 48g (1-1-67) and (2-24) Gamma-) Cyhalothrin) Cyhalothrin 22a (1-1-29) and ( 2-1) 49a (1-1-68) and (2-1) Acrinathrin) Acrinathrin 22b (1-1-29) and (2-3) 49b (1-1-68) and (2-3) Betacyfluthrin) Betacyfluthrin 22c (1-1-29) and (2-5) 49c (1-1-68) and (2-5) ) Cypermethrin) Cypermethrin 22d (1-1-29) and (2-6) 49d (1-1-68) and (2-6) ) Deltamethrin) Deltamethrin Product combination Product combination Nr. Active Nr., Which contains assets, which contains 22e (1-1-29) and (2-12) 49e (1-1-68) and (2-12) ) Lambda-Cyhalothrin) Lambda-Cyhalothrin 22f (1-1-29) and (2-14) 49f (1-1-68) and (2-14) Taufluvalinat) Taufluvalinat 22g (1-1-29) and (2-24) Gamma- 49g (1-1-68) and (2-24) Gamma-) Cyhalothrin) Cyhalothrin 23a (1-1-30) y ( 2-1) 50a (1-1-69) and (2-1) Acrinathrin) Acrinathrin 23b (1-1-30) and (2-3) 50b (1-1-69) and (2-3) Betacyfluthrin) Betacyfluthrin 23c (1-1-30) and (2-5) 50c (1-1-69) and (2-5) ) Cypermethrin) Cypermethrin 23d (1-1-30) and (2-6) 50d (1-1-69) and (2-6) Deltamethrin) Deltamethrin 23e (1-1-30) and (2-12) 50e (1-1-69) and (2-12) ) Lambda-Cyhalothrin) Lambda-Cyhalothrin 23f (1-1-30) and (2-14) 50f (1-1-69) and (2-14) Taufluvalinat) Taufluvalinat 23g (1-1-30) and (2-24) Gamma- 50g (1-1-69) and (2-24) Gamma-) Cyhalothrin) Cyhalothrin 24a (1-1-31) and ( 2-1) 51a (1-1-70) and (2-1) Acrinathrin) Acrinathrin Combination of products Combination of products Nr. Active Nr., Which contains assets, which contains 24b (1-1-31) and (2-3) 51b (1-1-70) and (2-3) Betacyfluthrin) Betacyfluthrin 24c (1-1-31) and (2-5) 51c (1-1-70) and (2-5) ) Cypermethriñ ') Cypermethrin 24d (1-1-31) and (2-6) 51d (1-1-70) and (2-6) Deltamethrin) Deltamethrin 24e (1-1-31) and (2-12) 51e (1-1-70) and (2-12) ) Lambda-Cyhalothrin) Lambda-Cyhalothrin 24f (1-1-31) and (2-14) 51f (1-1-70) and (2-14) Taufluvalinat) Taufluvalinat 24g (1-1-31) and (2-24) Gamma- 51g (1-1-70) and (2-24) Gamma-) Cyhalothrin) Cyhalothrin 25a (1-1-32) and ( 2-1) 52a (1-1-71) and (2-1) Acrinathrin) Acrinathrin 25b (1-1-32) and (2-3) 52b (1-1-71) and (2-3) Betacyfluthrin) Betacyfluthrin 25c (1-1-32) and (2-5) 52c (1-1-71) and (2-5) ) Cypermethrin) Cypermethrin 25d (1-1-32) and (2-6) 52d (1-1-71) and (2-6) Deltamethrin Deltamethrin > 25e (1-1-32) and (2-12) 52e (1-1-71) and (2-12) ) Lambda-Cyhalothrin i Lambda-Cyhalothrin Product combination Product combination Nr. Active Nr., Which contains assets, which contains 25f (1-1-32) and (2-14) 52f (1-1-71) and (2-14) Taufluvalinat) Taufluvalinat 25g (1-1-32) and (2-24) Ga ma- 52g (1-1-71) and (2-24) Gamma-) Cyhalothrin) Cyhalothrin 26a (1-1-33) and (2-1) 53a (1-1-72) and (2-1) Acrinathrin) Acrinathrin 26b (1-1-33) and (2-3) 53b (1-1-72) and (2-3) Betacyfluthrin) Betacyfluthrin 26c (1-1-33) and (2-5) 53c (1-1-72) and (2-5) ) Cypermethrin) Cypermethrin 26d (1-1-33) and (2-6) 53d (1-1-72) and (2-6) Deltamethrin) Deltamethrin 26e (1-1-33) and (2-12) 53e (1-1-72) and (2-12) ) Lambda-Cyhalothrin) Lambda-Cyhalothrin 26f (1-1-33) and (2-14) 53f (1-1-72) and (2-14) Taufluvalinat) Taufluvalinat 26g (1-1-33) and (2-24) Gamma- 53g (1-1-72) 'and (2-24) Gamma-) Cyhalothrin) Cyhalothrin 27a (1-1-38) and (2-1)) Acrinathrin 27b (1-1-38) and (2-3)) Betacyfluthrin Product combination Product combination Nr. Active Nr., Which contains assets, which contains 27c (1-1-38) and (2-5)) Cypermethrin 27d (1-1-38) and (2-6)) Deltamethrin 27e (1-1-38) and (2-12)) Lambda-Cyhalothrin 27f (1-1-38) and (2-14)) Taufluvalinat 27g (1-1-38) and (2-24) Gamma-) Cyhalothrin However, the definitions of the remains or the explanations given above in a general manner or indicated in the preferred ranges may be combined arbitrarily with each other, ie between the respective preferred ranges and intervals. These are valid, correspondingly, for the final products as well as for the products of departure and for the intermediate products. According to the invention, combinations of the active compounds containing the compounds of the formula (I) and pyrethroids of the formulas (2-1) to (2-24), in which the individual residues have a combination of the meanings indicated above as preferred (preferably). According to the invention, combinations of the active compounds containing the compounds of the formula (I) and pyrethroids of the formulas (2-1) to (2-24), in which the individual residues have a combination, are particularly preferred. of the meanings indicated above as being especially preferred. According to the invention, combinations of the active compounds containing the compounds of the formula (I) and pyrethroids of the formulas (2-1) to (2-24) will be very particularly preferred., wherein the individual residues have a combination of the meanings indicated above as being very particularly preferred. The saturated or unsaturated hydrocarbon radicals, such as alkyl or alkenyl, can be, even in combination with heteroatoms, such as, for example, alkoxy, as far as possible, respectively straight-chain or branched chain. The substituted radicals, if appropriate, can be monosubstituted or polysubstituted, the substituents being the same or different in the case of a polysubstantiation. The product combinations? Active ingredients may also contain other components of the mixture with fungicidal, acaricidal or insecticidal action. When the active compounds are present in the active compound combinations, in accordance with the invention, in certain proportions by weight, the synergistic effect will be particularly evident. However, the proportions by weight of the active products may vary in the combinations of active products within a relatively broad range. In general, the combinations, according to the invention, have the active product of the formula (I) and the mixture components of group 2 in the preferred and especially preferred mixing ratios indicated: * The proportions of the mixture are based on the proportions by weight. The proportion must be understood as the active product of the formula (I): component of the mixture The combinations of the active products are suitable for the fight against animal pests, preferably against arthropods and nematodes, especially against insects and arachnids, which occur in agriculture, in animal health, in forestry, for the protection of stored products. and of the materials as well as in the hygiene sector. These are active against normally sensitive and resistant species as well as against all or against individual stages of development. The pests mentioned above belong to: the order of the Isopoda for example, Oniscus asellus, Armadillidium vulgare, Porcellio scaber. From the order of the Diplopoda, for example, Blaniulus guttulatus. From the order of the Chilopoda, for example, Geophilus carpophagus, Scutigera spp. From the order of the Symphyla, for example, Scutigerella immaculata. From the order of the Thysanura, for example, Lepisma saccharina. From the order of the Colle ball, for example, Onychiurus armatus. From the order of Orthoptera, for example, Acheta domesticus, Gryllotalpa spp., Locusta migratoria migratorioides, Melanoplus spp., Schistocerca gregaria. From the order of the Blattaria, for example Blatta orientalis, Periplaneta americana, Leucophaea maderae, Germanic Blattella, From the order of the Dermaptera, for example, Forfícula auricularia. From the order of the Isoptera, for example, Reticulitermes spp .. From the order of Phthiraptera, for example Pediculus humanus corporis, Haematopinus spp., Linognathus spp., Trichodectes spp., Damalinia spp. From the order of the Thysanoptera, for example, Hercinothrips femoralis, Thrips tabaci, Thrips palmi, Fankliniella accidentalis .. From the order of the Heteroptera, for example, Eurygaster spp., Dysdercus intermedius, Piesma quadrata, Cimex lectularius, Rhodnius prolixus, Triatoma spp. From the order of the homoptera, for example , Aleurodes brassicae, Bemisia tabaci, Trialeurodes vaporariorum, Aphis gossypii, Brevicoryne brassicae, Cryptomyzus ribis, Aphis fabae, Aphis pomi, Eriosoma lanigerum, Hyalopterus arundinis, Phylloxera vastatrix, Pemphigus spp., Macrosiphum avenae, Myzus spp., Phorodon humuli, Rhopalosiphum padi , Empoasca spp., Euscelis bilobatus, Nephotettix cincticeps, Lecanium corni, Saissetia oleae, Laodephax striatellus, Nilaparvata lugens, Aonidiella aurantii, Aspidiotus hedera e, Pseudococcus spp. and Psylla spp. From the order of the Lepidoptera, for example, Pectinophora gossypiella, Bupalus piniarius, Cheimatobia brumata, Lithocolletis blancardella, Hyponomeuta padella, Plutella xylostella, Malacosoma * neustria, Euproctis chrysorrhoea, Lymantria spp., Bucculatrix thurberiella, Phyllocnistis citrella, Agrotis spp., Euxoa spp., Feltia spp., Earias insulana, Heliothis spp., Mamestra brassicae, Panolis flammea , Spodoptera spp., Trichoplusia ni, Carpocapsa pomonella, Pieris spp., Chilo spp., Pyrausta nubilalis, Ephestia kuehniella, Galleria mellonella, Tineola bisselliella, Tinea pellionella, Hofmannophila pseudospretella, Cacoecia podana, Capua reticulana, Choristoneura fumiferana, Clysia ambiguella, Homona magnanimous, Tortrix viridana, Cnaphalocerus spp., Oulema oryzae. From the order of the Coleoptera, for example, Anobium punctatum, Rhizopertha dominica, Bruchidius obtectus, Acanthoscelides obtectus, Hylotrupes bajulus, Agelastica alni, Leptinotarsa decemlineata, Phaedon cochleariae, Diabrotica spp., Psylliodes chrysocephala, Epilachna varivestis, Atomaria spp., Oryzaephilus surinamensis, Anthonomus spp., Sitophilus spp., Otiorrhynchus sulcatus, Cosmopolites sordidus, Ceuthorrhynchus assimilis, Hypera postica, Dermestes spp., Trogoderma spp., Anthrenus spp., Attagenus spp., Lyctus spp., Meligethes aeneus, Ptinus spp., Niptus hololeucus, Gibbium psylloides, Tribolium spp., Tenebrio molitor, Agriotes spp., Conoderus spp., Melolontha melolontha, Amphimallon solstitialis, Costelytra zealandica, Lissorhoptrus oryzophilus .. From the order of Hymenoptera, for example, Diprion spp., Hoplocampa spp. ., Lasius spp., Monomorium pharaonis, Vespa spp. From the order of the Diptera, for example, Aedes spp., Anopheles spp., Culex spp., Drosophila melanogaster, Musca spp., Fannia spp., Calliphora erythrocephala, Lucilia spp. ., Chrysomya spp., Cuterebra spp., Gastrophilus spp., Hyppobosca spp., Stomoxys spp., Oestrus spp., Hypoderma spp., Tabanus spp., Tannia spp., Bibio hortulanus, Oscinella frit, Phorbia spp., Pegomyia hyoscyami. , Ceratitis capítata, Dacus oleae, Typula paludosa, Hylemyia spp., Liriomyza spp. From the order of the Siphonaptera, for example, Xenopsylla cheopis, Ceratophyllus spp. From the class of the Arachnida, for example, Scorpio maurus, Latrodectus mactans, Acarus siró, Argas spp., Ornithodoros spp. ., Dermanyssus gallinae, Eriophys ribis, Phyllocoptruta oleivora, Boophilus spp., Rhipicephalus spp., Amblyomma spp., Hylamma spp., Ixodes spp., Psoroptes spp., Chorioptes spp., Sarcoptes spp., Tarsonemus spp., Bryobia praetiosa, Panonychus spp., Tetranychus spp., Hemitarsonemus spp. , Brevipalpus spp. Plant parasitic nematodes include, for example, Pratylenchus spp., Radopholus similis, Ditylenchus dipsaci, Tylenchulus semipenetrans, Heterodera spp., Globodera spp., Meloidogyne spp., Aphelenchoides spp., Longidorus spp., Xiphinema spp., Trichodorus spp., Bursaphelenchus spp. The active compound combinations according to the invention can be transformed in the usual formulations, such as solutions, emulsions, injectable powders, suspensions, powders, dusts, pastes, soluble powders, granules, suspension-emulsion concentrates, natural and synthetic materials impregnated with the active product, as well as microencapsulated in materials polymers. These formulations are prepared in known manner, for example by mixing the active ingredients with extenders, ie with liquid solvents and / or solid excipients, optionally with the use of surfactants, ie emulsifiers and / or dispersants and / or foam generating means. When water is used as an extender, organic solvents may be used, for example, as auxiliary solvents. Preferred liquid solvents are: aromatic hydrocarbons, such as xylene, toluene or alkylnaphthalenes, chlorinated aromatic hydrocarbons and chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, for example petroleum fractions, mineral and vegetable oils, alcohols such as butanol or glycol, as well as their ethers and esters, ketones, such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, or strongly polar solvents, such as such as dimethylformamide and dimethyl sulfoxide as well as water. Suitable solid excipients are, for example, ammonium salts and natural mineral flours, such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth and the synthetic minerals ground, such as highly dispersed silicic acid, the aluminum oxide and silicates; Suitable solid excipients for granules are, for example, broken and fractionated natural minerals, such as calcite, marble, pumice, sepiolite, dolomite, as well as synthetic granules of inorganic and organic flours as well as granules of organic material, such as sawdust, coconut husks, corn ears and tobacco stems; Suitable emulsifiers and / or foam generators are, for example, non-ionogenic and anionic emulsifiers, such as polyoxyethylenated esters of fatty acids, polyoxyethylenated ethers of fatty alcohols, for example, alkylaryl polyglycol ether, sulfonates of alkyl, the alkyl sulphates, the aryl sulfonates, as well as the albumin hydrolysates; Dispersants are suitable as dispersants: for example, sulphite lignin liquors and methylcellulose. In the formulations, adhesives such as carboxymethylcellulose, natural and synthetic polymers powdery, granulated or in the form of latex, such as gum arabic, polyvinyl alcohol, polyvinyl acetate, as well as natural phospholipids such as cephalins and lecithins, and synthetic phospholipids can be used. Other additives can be mineral and vegetable oils . Dyes, such as inorganic pigments, for example, iron oxide, titanium oxide, Prussian blue and organic dyes, such as metallic alizarin, azo and phthalocyanine dyes, as well as trace nutrients, such as iron salts, can be employed. of manganese, boron, copper, cobalt, molybdenum and zinc. The formulations contain, in general, between 0.1 and 95% by weight of active compound, preferably between 0.5 and 90%.

The active compound combinations, according to the invention, can be present in their commercially available formulations as well as in the forms of application prepared from these formulations, in mixture with other active products, such as insecticides, baits, sterilizers, bactericides, acaricides, nematicides, fungicides, growth regulating products or herbicides. Insecticides include, for example, esters of phosphoric acid, carbamates, esters of carbonic acid, chlorinated hydrocarbons, phenylureas, products prepared by means of microorganisms and the like. A mixture with other known active ingredients, such as herbicides or with fertilizers and growth regulators is also possible. The active compound combinations, according to the invention, can also be presented, when used as insecticides, in their customary formulations in commerce as well as in the forms of application prepared from these formulations in mixture with synergists. The synergists are the compounds by which the effect of the active products is increased, without the added synergist having to be active in itself. The active product content of the application forms, prepared from the usual commercial formulations, can vary within wide limits. The active compound concentration of the application forms can be between 0.0000001 to 95% by weight of active compound, preferably between 0.0001 and 1% by weight. The application is carried out in a manner adapted to the forms of application. In the use against hygiene pests and stored products, combinations of active products are characterized by an excellent residual effect on wood and clay as well as good stability to alkalis on limed substrates. The active compound combinations according to the invention are not only active against plant pests, hygiene and stored products, but also in the field of veterinary medicine against animal parasites (ectoparasites) such as ticks. hard, soft ticks, scabies mites, migratory mites, flies (suckers and mincers), fly parasitic larvae, lice, hair nits, feathered nits and fleas. To these parasites belong: From the order of the Anoplurida, for example Haematopinus spp., Linognathus spp., Pediculus spp., Phtirus spp., Solenopotes spp. From the order of the Mallophagida and the suborders Amblycerina as well as Ischnocerina, for example Trimenopon. spp., Menopon spp., Trinoton spp., Bovicola spp., Werneckiella spp. , Lepikentron spp. , Damalina spp. , Trichodectes spp. , Felicola spp. From the order of the Diptera and the suborders Nematocerina as well as Branchycerina, for example Aedes spp., Anopheles spp., Culex spp., Simulium spp., Eusimulium spp., Phlebotomus spp., Lutzomyia spp., Culicoides spp., Chrysops spp., Hybomitra spp., Atylotus spp., Tabanus spp., Haematopota spp., Philipomyia spp., Braula spp., Musca spp., Hydrotaea spp., Stomoxys spp., Haematobia spp., Morellia spp. , Fannia spp., Glossina spp., Calliphora spp., Lucilia spp., Chrysomya spp., Wohlfahrtia spp., Sarcophaga spp., Oestrus spp., Hypoderma spp., Gasterophilus spp., Hippobosca spp., Lipoptena spp., Melophagus. spp. From the order of the Siphonapterida, for example Pulex spp., Ctenocephalides spp., Xenopsylla spp., Ceratophyllus spp. From the order of the Heteropteridae, for example Cimex spp., Triatoma spp., Rhodnius spp., Panstrongylus spp. From the order of the Blattarida, for example, Blatta orientalis, Periplaneta americana, Blattella germanica, Supella spp. From the subclass of the A caria (Acarida) and the order of the meta- as well as mesoestigmatos, for example Argas spp., Ornithodorus spp. , Otobius spp. , Ixodes spp. , Amblyomma spp. , Boophilus spp., Dermacentor spp., Haemaphysalis spp., Hyalomma spp., Rhipicephalus spp., Dermanyssus spp., Raillietia spp., Pneumonyssus spp., Stemostoma spp., Varroa spp. From the order of the Actinedida (Prostigmata) and acaridids (Astigmata), for example 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. , Laminosioptes spp .. The active compound combinations, according to the invention, are also suitable for the fight against arthropods, which attack animals useful in agriculture such as, for example, cows, lambs, goats, horses, pigs , asses, camels, buffaloes, rabbits, chickens, turkeys, ducks, geese, bees, other domestic animals such as, for example, dogs, cats, game birds, aquarium fish as well as so-called test animals, such as , for example, hamsters, guinea pigs, rats and mice. Through the fight against these arthropods, cases of death and reductions in productivity (in milk, meat, wool, skins, eggs, honey, etc.) will be avoided, so that by using the active products according to the invention , a more economical and simpler maintenance of the animals is possible. The application of the active compound combinations, according to the invention, is carried out in the veterinary sector in a known manner by enteral administration in the form of, for example, tablets, capsules, beverages, dragees, granules, pastes, bolis, by means of the procedure through the feed-through feed, of suppositories, by parenteral administration, such as, for example, by injection (intramuscular, subcutaneous, intravenous, intraperitoneal and the like), implants, by nasal application, by application through the skin in the form, for example of immersion or bathing (Dippen), sprayed. (Spray), surface watering (Pour-on and Spot-on), washing, dusting as well as with the aid of molded bodies containing the active product such as collars, ear tags, tails for the tail, bands for the ears limbs, halters, marking devices, etc. When used for domestic livestock, poultry, pets, etc. the active ingredients can be used as formulations (for example powders, emulsions, agents capable of spreading), containing the active compounds in amounts of 1 to 80% by weight, directly or after dilution of 100 to 10,000 times or can be used as a solvent. chemical bath Furthermore, it has been found that the combinations of the active compounds according to the invention show a high insecticidal effect against insects, which destroy industrial materials. By way of example and preference - however without limitation - the following insects may be mentioned: Beetles, such as Hylotrupes bajulus, Chlorophorus pilosis, Anobium punctatum, Xestobium rufovillosum, Ptilinus pecticornis, Dendrobium pertinex, Ernobius mollis, Priobium carpini, Lyctus brunneus, Lyctus africanus, Lyctus planicollis, Lyctus linearis, Lyctus pubescens, Trogoxylon aequale, Minthes rugicollis; Xyleborus spec. , Tryptodendron spec, Apate monachus, Bostrychus capucins, Heterobostrychus brunneus, Sinoxylon spec., Dinoderus minutus. Hymenoptera, such as Sirex juvencus, Urocerus gigas, Urocerus gigas taignus, Urocerus augur. Termites, such as Kalotermes flavicollis, Cryptotermes brevis, Heterotermes indicala, Reticulitermes flavipes, Reticulitermes santonensis, Reticulitermes lucifugus, Mastotermes give iniensis, Zootermopsis nevadensis, Coptotermes formosanus. Thysanides, such as Lepisma saccharina. By industrial materials, non-living materials will be understood in the present context, such as, preferably, synthetic materials, glues, glues, paper and cardboard, leather, wood and wood processing products and paints. In a very special way, the materials to be protected against attack by insects are made of wood and wood products. By wood and wood processing products, which can be protected by means of the agents according to the invention or of the mixtures containing them, it should be understood, for example: construction wood, wooden beams, railway sleepers , parts for bridges, ribs for boats, wooden vehicles, boxes, pallets, containers, telephone poles, wooden coatings, wooden windows and doors, wooden plywood, plywood plates, carpentry works or wood products, which find application , in a very general way, at home or in the construction industry. The active compound combinations can be used as such, in the form of concentrates or of customary formulations in general such as powders, granules, solutions, suspensions, emulsions or pastes. Said formulations can be prepared in a manner known per se, for example by mixing the active compounds with at least one solvent or diluent, emulsifier, dispersant and / or binder or binding agent, water repellent, optionally drying agents and stabilizers. against UV and, if necessary, dyes and pigments as well as other processing aids. The insecticidal agents or concentrates to be used for the protection of wood and wood materials contain the active compound according to the invention in a concentration of 0.0001 to 95% by weight, in particular 0.001 to 60% by weight. weight. The quantity of the agents or concentrates used depends on the type and origin of the insects and the environment. The optimum application amount can be determined respectively by means of series of tests prior to application. However, it is generally sufficient to employ from 0.0001 to 20% by weight, preferably from 0.001 to 10% by weight of the active compound, based on the material to be protected. A solvent or a mixture of organochemical solvents and / or a solvent or mixture of organo-chemical, oleaginous or oil-like solvents, which are difficult to volate and / or a solvent or mixture of polar organochemical solvents, is used as solvent and / or diluent. and / or water and, if appropriate, an emulsifier and / or humectant. The organochemical solvents used are preferably oleaginous or oleaginous solvents, with an evaporation index above 35 and a flame point above 30 ° C, preferably above 45 ° C. By way of such water-insoluble, oil-insoluble or oleaginous-type solvents which are difficult to volatile, corresponding mineral oils or their aromatic fractions or solvent mixtures containing mineral oils will be used., preferably benzine for tests, petroleum and / or alkylbenzene. Advantageously, mineral oils with a boiling range of 170 to 220 ° C, benzine for tests with a boiling range of 170 to 220 ° C, spindle oil with a boiling range of 250 to 350 ° C, petroleum or either aromatic hydrocarbons with a boiling range of 160 to 280 ° C, terpene oil and the like. In a preferred embodiment, liquid aliphatic hydrocarbons having a boiling range of 180 to 210 ° C or a high-boiling mixture of aromatic and aliphatic hydrocarbons having a boiling range of 180 to 220 ° C and / or spindles and / or monochloronaphthalene, preferably a-monochloronaphtalin. Organic solvents, which are difficult to volatile, oleaginous or oil-based, with an evaporation index above 35 and with a flame point above 30 ° C, preferably above 45 ° C, can be partially replaced by solvents light or medium volatility organochemicals, provided that the solvent mixture has an evaporation index above 35 and a flame point above 30 ° C, preferably above 45 ° C, and that the insecticidal-fungicidal mixture is soluble or emulsifiable in this mixture of solvents. According to a preferred embodiment, a part of the solvent or mixture of organochemical solvents or a solvent or mixture of aliphatic, polar organochemical solvents will be replaced. Preferably, aliphatic organochemical solvents containing hydroxyl and / or ester and / or ether groups, such as, for example, glycol ethers, esters or the like, will be used. As organic-chemical binders, synthetic resins and / or setting drying oils, known per se, dilutable with water and / or soluble or dispersible or emulsifiable in the organic-chemical solvents used, will be used within the scope of the present invention. especially binders consisting of or containing acrylic resin, a vinyl resin, for example polyvinyl acetate, polyester resin, polycondensation or polyaddition resin, polyurethane resin, alkyd resin or modified alkyd resin, phenolic resin, hydrocarbon resin such as indeno-coumaron resin, silicone resin, vegetable drying and / or drying oils and / or physical drying binders based on a natural and / or synthetic resin. The synthetic resin, used as a binder, can be used in the form of an emulsion, dispersion or solution. Bitumen or bituminous substances up to 10% by weight can also be used as binders. In a complementary manner, colorants, pigments, water-repelling agents, odor correctors and inhibitors or anticorrosive agents known per se and the like can be used.

It is preferred to use at least one alkyd resin or a modified alkyd resin and / or a drying vegetable oil in the medium or concentrate according to the invention as an organochemical binder. Preferably, alkyd resins having an oil content of greater than 45% by weight, preferably from 50 to 68% by weight, are preferably used according to the invention. The aforementioned binder can be partially or totally replaced by a fixing agent (mixture) or by a plasticizer (mixture). These additives should avoid volatilization of active products as well as crystallization or precipitation. They preferably replace 0.01 to 30% of the binder (based on 100% of the binder used). The plasticizers are of the chemical class of phthalic acid esters such as dibutyl, dioctyl or benzylbutyl phthalate, phosphoric acid esters, such as tributyl phosphate, esters of adipic acid, such as di- (D-adipate). 2-ethylhexyl), stearates such as butyl stearate or amyl stearate, oleates such as butyl oleate, glycerin ethers or high molecular weight glycol ethers, glycerin esters as well as esters of p-toluenesulfonic acid. Fixative agents are chemically based on polyvinylalkyl ethers such as polyvinyl methyl ether or ketones such as benzophenone, ethylenebenzophenone. Suitable as solvent or diluent is water, optionally mixed with one or more of the aforementioned solvents or diluents, emulsifiers and organochemical dispersants. Especially effective protection of the wood is achieved by impregnation processes on an industrial scale, for example vacuum, double vacuum or pressure processes. At the same time, the combinations of the active compounds according to the invention can be used for the protection against the proliferation of organisms on objects, especially on the bodies of ships, screens, networks, constructions, port facilities and signaling installations, which enter in contact with seawater or brackish water. The proliferation of organisms due to sessile Oligochaeten, such as calcareous tubicides as well as due to bivalves and species of the lepadomorphs group (sea acorns), such as various types of Lepas and Scalpellum or due to types of the group of the balanomorphs ( barnacles), such as Balanus species, or Pollicipes, increase the resistance to friction of ships and leads, as a result of increased energy consumption and also due to frequent dry dock stays, to a clear increase in the costs of exploitation. In addition to the proliferation of organisms due to algae, for example Ectocarpus sp. and Ceramium sp., has a special significance in particular the proliferation of organisms due to sessile groups of entomostráceos, which are grouped under the name of Cirripedia (crustáceos cirrípedos). It has now been found, surprisingly, that the combinations of the active compounds according to the invention have an excellent anti-fouling effect (antiproliferation of organisms). By using the combinations of the active compounds according to the invention, the use of heavy metals, for example in the sulfides of bis (trialkyltin), tri-n-butyltin laurate, tri-n-butyltin chloride, can be abandoned. , cuprous oxide (I), triethyltin chloride, tri-n-butyl- (2-phenyl-4-chlorophenoxy) -tin, tributyltin oxide, molybdenum disulfide, antimony oxide, polymer butyl lithium, phenyl- (bispyridine) chloride ) -bismuth, tri-n-butyltin fluoride, manganese ethylenebistiocarbamate, zinc dimethyldithiocarbamate, zinc ethylenebistiocarbamate, zinc and copper salts of 2-pyridinium-l-oxide, bisdimethyldithiocarbamoylcycline ethylenebistiocarbamate, zinc oxide, cuprous ethylene-bisdithiocarbamate (I), copper thiocyanate, copper naphthenate and tributyltin halides or the concentration of these compounds can be decisively reduced. Furthermore, antifouling paints ready for application contain, if necessary, other active ingredients, preferably algicides, fungicides, herbicides, molluscicides or other antifouling active agents. As components of the combination for the antifouling agents, according to the invention, preferably, they are suitable: algicides such as 2- tere. -butylamino-4-cyclopropylamino-6-methylthio-l, 3, 5-triazine, Dichlorophen, Diuron, Endothal, Fentinacetat, Isoproturon, Methabenzthiazuron, Oxyfluorfen, Quinoclamine and Terbutryn; fungicides such as S, S-dioxide of benzo [b] -thiophenecarboxylic acid cyclohexylamide, Dichlofluanid, Fluorfolpet, 3-iodo-2-propynyl-butylcarbamate, Tolylfluanid and azoles such as Azaconazole, Cyproconazole, Epoxyconazole, Hexaconazole, Metconazole, Propiconazole and Tebuconazole; molluscicides such as Fentinacetat, Metaldehyd, Methiocarb, Niclosamid, Thiodicarb and Trimethacarb; or traditional anti-fouling agents such as 4,5-dichloro-2-octyl-4-isothiazolin-3-one, diiodomethyl paratrysulfone, 2- (N, N-dimethylthiocarbamoylthio) -5-nitrothiazyl, potassium, copper, sodium salts and zinc of 2-pyridinium-l-oxide, pyridine-triphenylborane, tetrabutyldistannoxane, 2,3,5,6-tetrachloro-4- (methylsulfonyl) -pyridine, 2,4,5,6-tetrachloroisophthalonitrile, tetramethylthiouram disulfide and 2,4,6-trichlorophenylmaleinimide. The antifouling agents used contain the active compound combinations according to the invention in a concentration of 0.001 to 50% by weight, in particular 0.01 to 20% by weight. The anti-fouling agents according to the invention also usually contain the frequent components, but are not limited thereto, such as, for example, those described in Ungerer, Chem. Ind. 1985, 37, 730-732 and Williams, Antifouling Marine Coatings, Noyes, Park Ridge, 1973. The antifouling paints contain, in addition to the active ingredients, algaecides, fungicides, molluscicides and insecticides according to the invention, especially binders. Examples of recognized binders are polyvinyl chloride in a solvent system, chlorinated rubber in a solvent system, acrylic resins in a solvent system especially in an aqueous system, vinyl chloride / vinyl acetate copolymer systems in the form of aqueous dispersions or form of systems in organic solvents, butadiene / styrene / acrylonitrile rubbers, desiccant oils such as linseed oil, resin esters or resin esters modified in combination with tars or bitumen, asphalt and epoxy compounds, small amounts of chlorinated rubber, chlorinated polypropylene and resins vinyl. If appropriate, the paints also contain inorganic pigments, organic pigments or dyes, which are preferably insoluble in seawater. In addition the paints may contain materials such as colophonium to enable a controlled release of the active products. The paints may also contain plasticizers, modifying agents that influence the rheological properties as well as other traditional components. Also in self-polishing anti-fouling systems, the compounds according to the invention or the aforementioned mixtures can be incorporated. The combinations of the active compounds, according to the invention, are suitable for combating animal pests, especially insects, arachnids and mites, which occur in closed enclosures, such as, for example, houses, manufacturing facilities, offices, cabins of motor vehicles and the like. These can be used to combat these pests in insecticide products for the home. These are active against sensitive and resistant types as well as against all stages of development. To these pests belong: From the order of the Scorpionidea, for example, Buthus occitanus. From the order of the Acariña, for example, Argas persicus, Argas reflexus, Bryobia ssp., Dermanyssus gallinae, Glyciphagus domesticus, Ornithodorus moubat, Rhipicephalus sanguineus, Trombicula alfreddugesi, Neutrombicula autumnalis, Dermatophagoides pteronissimus, Dermatophagoides forinae. From the order of the Araneae, for example Aviculariidae, Araneidae. From the order of the Opiliones, for example Pseudoscorpiones chelifer, Pseudoscorpiones cheiridium, Opiliones phalangium. From the order of the Isopoda, for example, Oniscus asellus, Porcellio scaber. From the order of the Diplopoda, for example, Blaniulus guttulatus, Polydesmus spp. From the order of the Chilopoda, for example, Geophilus spp. From the order of the Zygentoma, for example, Ctenolepisma spp., Lepisma sacharina, Lepismodes inquilinus. From the order of the Blattaria, for example Blatta orientalies, Germanic Blattella, Blatella asahinai, Leucophaea maderae, Panchlora spp., Parcoblatta spp., Periplaneta australasiae, Periplaneta americana, Periplaneta brunnea, Periplaneta fuliginosa, Supella longipalpa.

From the order of the Saltatoria, for example, Acheta domesticus. From the order of the Dermaptera, for example, Forfícula auricularia. From the order of the Isoptera, for example, Kalotermes spp., Reticulitermes spp. From the order of the Psocoptera, for example, Lepinatus spp., Liposcelis spp. From the order of the Coleptera, for example, Anthrenus spp., Attagenus spp., Dermestes spp., Latheticus oryzae, Necrobia spp., Ptinus spp., Rhizopertha dominica, Sitophilus granarius, Sitophilus oryzae, Sitophilus zeamais, Stegobium paniceum. From the order of the Diptera, for example, Aedes aegypti, Aedes albopictus, Aedes taeniorhynchus, Anopheles spp., Calliphora erythrocephala, Chrysozona pluvialis, Culex quinquefasciatus, Culex pipiens, Culex tarsalis, Drosophila spp., Fannia canicularis, Musca domestica, Phlebotomus spp. Sarcophaga carnaria, Simulium spp., Stomoxys calcitrans, Typula paludosa. From the order of the Lepidoptera, for example, Achroia grisella, Galleria mellonella, Plodia mterpunctella, Tinea cloacella, Tinea pellionella, Tineola bisselliella. From the order of the Siphonaptera, for example, Ctenocephalides canis, Ctenocephalides felis, Pulex irritans, Tunga penetrans, Xenopsylla cheopis.

From the order of Hymenoptera, for example, Camponotus herculeanus, Lasius fuliginosus, Lasius niger, Lasius umbratus, Monomorium pharaonis, Paravespula spp., Tetramorium caespitum. From the order of the Anoplura, for example Pediculus humanus capitis, Pediculus humanus corporis, Phthirus pubis. From the order of the Heteroptera, for example, Cimex hemipterus, Cimex lectularius, Rhodinus prolixus, Triatoma infestans. The application is carried out in aerosols, agents for spray without pressure, for example aerosols by pumping and by spray, automatic devices for the generation of aerosols, nebulizers, foam generators, gels, products for evaporators with platelets for cellulose evaporators or of synthetic material, liquid evaporators, gel and membrane evaporators, fan-driven evaporators, evaporative systems without energy consumption or passive, papers against moths, sachets against moths and gels against moths, in the form of granules or of dust, in dispersible baits or in stations for baits. All plants and parts of plants can be treated according to the invention. By plants, all plants and plant populations, such as desired and unwanted wild plants (including crop plants of natural origin), will be understood in this case. The crop plants can be plants that can be obtained by conventional methods and cultivation and optimization or by means of biotechnological and genetic engineering methods, including transgenic plants and including plant varieties that can be protected or not through the right of protection of plant varieties. By parts of the plants should be understood all parts and aerial and underground organs of plants, such as buds, leaves, flowers and roots, being able to indicate in an exemplary way leaves, needles, stems, trunks, flowers, fruit bodies, fruits and seeds as well as roots, tubers and rhizomes. The harvests as well as vegetative and generative reproductive material, for example seedlings, tubers, rhizomes, layering and seeds, also belong to the parts of the plants. The treatment, according to the invention, of plants and parts of the plants with the active products, is carried out directly or by action on their surroundings, on their environment or in the storage enclosures, in accordance with the usual treatment methods, for example by immersion, spraying, evaporation, fogging, spreading, brushing and, in the case of the reproduction material, especially in the case of seeds, also by coating with one or more layers. As already indicated above, all plants and their parts can be treated according to the invention. In a preferred embodiment, plants and plant varieties as well as parts thereof of wild origin or that are obtained by conventional methods of biological cultivation, such as crossing or fusion of protoplasts, are treated. In another preferred embodiment, plants and varieties of transgenic plants, which have been obtained according to genetic engineering methods if appropriate in combination with conventional methods (genetically modified organisms) and their parts are treated. The expression "parts" or "parts of plants" or "components of plants" has been previously explained. In accordance with the invention, plants of the plant varieties customary in the trade or in use will be treated with particular preference. According to the types of plants or the plant varieties, their location and the growth conditions (soil, climate, vegetation period, food) can also be presented by means of the treatment according to the invention over-additive effects ( "synergistic"). In this way, for example, smaller amounts of application and / or enlargements of the activity spectrum and / or a strengthening of the effect of the products employable according to the invention are possible, better growth of the plants, greater tolerance to high temperatures or low, greater tolerance against drought or against the salt content of water or soil, greater floral yield, easier harvesting, acceleration of maturation, higher yields of crops, higher quality and / or higher nutritive value of collected products, greater storage capacity and / or transformation of the products collected, which go beyond the expected effect itself. To plants or varieties of transgenic plants (Genetically engineered) to be treated preferably according to the invention, belong all plants, which have acquired genetic material by modification by genetic engineering, which provide these plants with particularly advantageous valuable properties ("characteristics"). Examples of such properties are, better plant growth, greater tolerance to high or low temperatures, greater tolerance to drought or against the salt content of water or soil, higher floral yield, easier harvesting, acceleration of ripening, higher crop yields, higher quality and / or higher nutritional value of the harvested products, greater storage capacity and / or transformation of the products harvested. Other examples, especially noteworthy for such properties are the greater resistance of plants against animal and microbial pests, such as against insects, mites, phytopathogenic fungi, bacteria and / or viruses as well as a greater tolerance of plants against certain active herbicide products. Examples of transgenic plants are the important crop plants, such as cereals (wheat, rice), corn, soybeans, potatoes, cotton, tobacco, rapeseed as well as fruit tree plantations (with the fruits apple, pear, citrus and grape) , especially corn, soybeans, potatoes, cotton, tobacco and rapeseed. As properties ("characteristics"), the greater resistance of plants to insects will be pointed out by means of the toxins generated in plants, especially those generated in plants by the genetic material from Bacillus Thuringiensis (for example by of the genes Cry? A (a), Cry? A (b), Cry? A (c), CrylIA, CrylIIA, CryIIIB2, Cry9c, Cry2Ab, Cry3Bb and CrylF as well as their combinations), (hereinafter referred to as " Bt plants "). As properties ("characteristics"), the greater tolerance of plants against fungi, bacteria and viruses by means of systemically acquired resistance (SAR), systemin, phytoalexin, elicitors as well as resistance genes and proteins and toxins expressed from corresponding way. As properties ("characteristics"), in particular, the greater tolerance of the plants to certain herbicidally active products, for example imidazolinones, sulfonylureas, Glyphosate or Phosphinotricin (for example gene "PAT"), will be pointed out. The respective genes, which provide the desired properties ("characteristics") may also be present in combination with each other in the transgenic plants. Examples of "Bt plants" include maize varieties, cotton varieties, soya varieties and potato varieties, which are marketed under the trade names YIELD GARD® (for example corn, cotton, soybean), KnockOut® (for example corn), StarLink® (for example corn), Bollgard® (cotton), Nucotn® (cotton) and Ne Leaf® (potato). Examples of plants that tolerate herbicides include maize varieties, cotton varieties and varieties of soybeans, which are marketed under the trade names Roundup Ready® (tolerance to Glyphosate, for example corn, cotton, soy), Liberty Link ® (tolerance to Phosphinotricin, for example rapeseed), IMI® (tolerance to imidazolinones) and STS® (tolerance to sulfonylureas, for example corn). As herbicide-resistant plants (conventionally cultivated with tolerance to herbicides), the varieties marketed under the name Clearfield® (for example corn) can also be cited. Obviously these indications are valid also for varieties of plants that are developed in the future or that are marketed in the future with these properties ("characteristics") genetic or that develop in the future. The plants indicated can be treated in a particularly advantageous manner, according to the invention, with the active ingredient mixtures according to the invention. The preferred ranges, indicated above, for the mixtures, are also valid for the treatment of these plants. It should be noted especially the treatment of plants with the mixtures especially cited in this text. The good insecticidal and acaricidal effect of the combinations of the active compounds according to the invention is apparent from the following examples. While the individual active products have weak points in terms of their effect, the combinations show an effect that goes beyond the simple addition of the effects of the active products. There is a synergistic effect in the case of insecticides and acaricides provided that the effect of the combination of the active products is greater than the sum of the effects of the active products applied individually.

The expected effect for a given combination of two active products can be calculated in accordance with S.R. Coiby, Weeds, 15, (1967), 20-22) in the following manner: if X represents the degree of destruction, expressed in% of the untreated controls, when the active product A is used in an amount of mg application / ha or at a concentration of mg / ha, Y represents the degree of destruction, expressed in% of the untreated controls, when the active product B is used in an application amount of ng / ha or at a concentration of ng / ha, and E represents the degree of destruction, expressed in% of the untreated controls, when the active products A and B are used in amounts of application of m or n / ha or at a concentration of m and n / ha, then X-Y E =? + Y- 100 If the actual effect is greater than the calculated one, then the combination is superadditive in terms of its destructive effect, that is, a synergistic effect is present. In this case, the actual degree of destruction, observed, must be greater than the value calculated from the formula previously indicated for the expected degree of destruction (E).

After the desired time the destruction is determined in%. In this case 100% means that all the animals have been destroyed; 0% means that no animal has been destroyed. Application examples Example A Test with Myzus persicae Solvent: 7 parts by weight of dimethylformamide. Emulsifier: 2 parts by weight of alkylaryl polyglycol ether. To obtain a suitable preparation of active compound, 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier and the concentrate is diluted with water, containing emulsifier, to the desired concentration. Cabbage leaves (Brassica olerácea), which are strongly attacked by the peach aphid (Myzus persicae), are treated by immersion in the preparation of the active compound of the desired concentration. After the desired time the destruction is determined in percentage. In this case 100% means that all the aphids were destroyed; 0% means that no aphids were destroyed. The destruction values determined are calculated according to the Coiby formula (see page 39 of the German text). In this test, they show a synergistically reinforced activity, compared to active products, used individually, for example, combinations of the following active products, according to the present invention: Table Al: Insects harmful to plants. Test with Myzus persicae * gef = activity found ** ber. = activity calculated according to the Coiby formula Table A2: Harmful insects for plants Test with Myzus persicae * gef = activity found ** ber. = activity calculated according to the Coiby formula Example B Test with larvae of Phaedon cochleariae Solvent: 7 parts by weight of dimethylformamide. Emulsifier: 2 parts by weight of alkylaryl polyglycol ether. To obtain a suitable preparation of active compound, 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier and the concentrate is diluted with water, containing emulsifier, to the desired concentration. Cabbage leaves (Brassica oleracea) are treated by being dipped into the preparation of the active compound of the desired concentration and covered with larvae of the horseradish leaf beetle (Phaedon cochleariae), as long as the leaves are still moist. After the desired time the destruction is determined in percentage. In this case 100% means that all larvae of the beetles were destroyed; 0% means that no larvae of the beetles were destroyed. The determined destruction values are calculated according to the Coiby formula (see page 39 of the German text). In this test they show a reinforced activity in a synergistic way, in comparison with the active products, used individually, for example, the combinations of the following active compounds, according to the present invention: Table B: Insects harmful to plants Phaedon larvae cochleariae * gef = activity found ** ber. = activity calculated according to the Coiby formula Example C Test with Plutella-xylostella (resistant family) Solvent: 7 parts by weight of dimethylformamide. Emulsifier: 2 parts by weight of alkylaryl polyglycol ether. To obtain a suitable preparation of active comd, 1 part by weight of active comd is mixed with the indicated amounts of solvent and emulsifier and the concentrate is diluted with water, containing emulsifier, to the desired concentration. Cabbage leaves (Brassica olerácea) are treated by immersion in the preparation of the active product of the desired concentration and are covered with caterpillars of the cabbage moth (Plutella xylostella, resistant family), as long as the leaves are still moist. After the desired time the destruction is determined in percentage. In this case 100% means that all caterpillars were destroyed; 0% means that no caterpillar was destroyed. The determined destruction values are calculated according to the Coiby formula (see page 39 of the German text). In this test they show a reinforced activity in a synergistic way, in comparison with the active products, used individually, for example, the combinations of the following active products, in accordance with the present invention: Table Cl: Harmful insects for plants Test with Plutella-xylostella (resistant family) * gef = activity found ** ber. = activity calculated in accordance with the formula of Coiby Table C2: Insects harmful to plants Test with Plutella-xylostella (resistant family) * gef = activity found ** ber. = activity calculated in accordance with the Coiby formula Example D Test with Spodoptera frugiperda Solvent: 7 parts by weight of dimethylformamide. Emulsifier: 2 parts by weight of alkylaryl polyglycol ether. To obtain a suitable preparation of active comd, 1 part by weight of active comd is mixed with the indicated amounts of solvent and emulsifier and the concentrate is diluted with water, containing emulsifier, to the desired concentration. Cabbage leaves (Brassica olerácea) are treated by being dipped into the preparation of the active comd of the desired concentration and covered with caterpillars (Spodoptera frugiperda), as long as the leaves are still moist. After the desired time the destruction is determined in percentage. In this case 100% means that all caterpillars were destroyed; 0% means that no caterpillar was destroyed. The determined destruction values are calculated according to the Coiby formula (see page 39 of the German text). In this test they show a reinforced activity in a synergistic way, in comparison with the active products, used individually, for example, the combinations of the following active products, in accordance with the present invention: Table D: Harmful insects for plants Test with Spodoptera frugiperda * gef = activity found ** ber. = activity calculated in accordance with the Coiby formula It is noted that, with reference to this date, the best method known to the applicant to carry out the aforementioned invention is that which is clear from the present description of the invention.

Claims (6)

CLAIMS Having described the invention as above, the content of the following claims is claimed as property:

1. Agents, containing a combination of active products, with synergistic activity, constituted by anthranilic acid amides of the formula (I) characterized in that A1 and A2 signify, independently of each other, oxygen or sulfur, X1 signifies N or CR10, R1 signifies hydrogen or means alkyl having 1 to 6 carbon atoms, alkenyl having 2 to 6 carbon atoms, alkynyl having 2 to 6. carbon or cycloalkyl atoms with 3 to 6 carbon atoms each substituted, if appropriate, one or more times, the substituents being independently selected from R 6, halogen, cyano, nitro, hydroxy, alkoxy with 1 to 4 atoms of carbon, alkylthio with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, alkoxycarbonyl with 2 to 4 carbon atoms, alkylamino with 1 to 4 carbon atoms, dialkylamino with 2 to 8 carbon atoms, cycloalkylamino with 3 to 6 carbon atoms, (alkyl with 1 to 4 carbon atoms) cycloalkylamino with 3 to 6 carbon atoms or R2 means hydrogen, alkyl having 1 to 6 carbon atoms, alkenyl with 2 to 6 carbon atoms, alkynyl with 2 to 6 carbon atoms, cycloalkyl with 3 to 6 carbon atoms, alkoxy with 1 to 4 carbon atoms, alkylamino with 1 to 4 carbon atoms, dialkylamino with 2 to 8 carbon atoms, cycloalkylamino with 3 to 6 carbon atoms, alkoxycarbonyl with 2 to 6 carbon atoms or alkylcarbonyl with 2 to 6 carbon atoms, R3 means hydrogen, R11 or means alkyl with 1 to 6 carbon atoms, alkenyl with 2 to 6 carbon atoms, alkynyl with 2 to 6 carbon atoms, cycloalkyl with 3 to 6 carbon atoms, respectively substituted, if appropriate, once or several times, being able to choose the substituents, independently of each other, between Rs, halogen, cyano, nitro, hydroxy, alkoxy with 1 to 4 carbon atoms, halogenoalkoxy with 1 to 4 carbon atoms, alkylthio with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, at C 1 -C 4 -alkylsulfonyl, C 2 -C 6 -alkoxycarbonyl, C 2 -C 6 -alkylcarbonyl, C 3 -C 6 -alkylsilyl, R 11, phenyl, phenoxy, or a 5 or 6 membered heteroaromatic ring , where appropriate, each phenyl, phenoxy or heteroaromatic ring with 5 or 6 members can be substituted and substituents can be chosen, independently from each other, between one to three residues W or one or more residues R, or R2 and R3 can be joined together and form the ring M, R 4 means hydrogen, alkyl with 1 to 6 carbon atoms, alkenyl with 2 to 6 carbon atoms, alkynyl with 2 to 6 carbon atoms, cycloalkyl with 3 to 6 carbon atoms, haloalkyl with 1 to 6 carbon atoms, halogenalkenyl with 2 to 6 carbon atoms, halogenalkynyl with 2 to 6 carbon atoms, halogencycloalkyl with 3 to 6 carbon atoms, halogen, cyano, nitro, hydroxy, alkoxy with 1 to 4 carbon atoms carbon, hal Oxyalkoxy with 1 to 4 carbon atoms, alkylthio with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, halogenalkylthio with 1 to 4 carbon atoms, haloalkylsulfinyl with 1 to 4 carbon atoms, halogenalkylsulfonyl with 1 to 4 carbon atoms, alkylamino with 1 to 4 carbon atoms, dialkylamino with 2 to 8 carbon atoms, cycloalkylamino with 3 to 6 carbon atoms, trialkylsilyl with 3 to 6 carbon atoms or phenyl, benzyl or phenoxy substituted, if appropriate, one or more times, the substituents being independently selected from alkyl having 1 to 4 carbon atoms, alkenyl having 2 to 4 carbon atoms, alkynyl with 2 to 4 carbon atoms; carbon atoms, cycloalkyl with 3 to 6 carbon atoms, halogenalkyl with 1 to 4 carbon atoms, halogenalkenyl with 2 to 4 carbon atoms, halogenalkynyl with 2 to 4 carbon atoms, halogencycloalkyl with 3 to 6 carbon atoms, halogen, cyano, nitro, alkoxy with 1 to 4 carbon atoms, haloalkoxy with 1 to 4 carbon atoms carbon, alkylthio with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, alkylamino with 1 to 4 carbon atoms, dialkylamino with 2 to 8 carbon atoms, cycloalkylamino with 3 to 6 carbon atoms, (alkyl) cycloalkylamino with 3 to 6 carbon atoms, alkylcarbonyl with 2 to 4 carbon atoms, alkoxycarbonyl with 2 to 6 carbon atoms, alkylaminocarbonyl with 2 to 6 carbon atoms, dialkylaminocarbonyl with 3 to 8 carbon atoms carbon atoms or trialkylsilyl with 3 to 6 carbon atoms R8 respectively stand for, independently of one another, hydrogen, halogen or mean alkyl with 1 to 4 carbon atoms, haloalkyl with 1 to 4 carbon atoms no, R12, G, J, -OJ, -OG, -S (0) pJ, -S (0) pG, -S (O) p-phenyl substituted respectively, optionally, substituents being chosen, independently from yes, between one to three residues W or between R12, alkyl with 1 to 10 carbon atoms, alkenyl with 2 to 6 carbon atoms, alkynyl with 2 to 6 carbon atoms, alkoxy with 1 to 4 carbon atoms or alkylthio with 1 to 4 carbon atoms, each substituent, independently of one another, can be substituted by one or more substituents chosen from G, J, R6, halogen, cyano, nitro, amino, hydroxy, alkoxy with 1 to 4 carbon atoms, haloalkoxy with 1 to 4 carbon atoms, alkylthio with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, halogenalkylthio with 1 to 4 carbon atoms, haloalkylsulfinyl with 1 to 4 atoms of carbon, halogenalkylsulfonyl with 1 to 4 carbon atoms, alkylamino with 1 to 4 carbon atoms , dialkylamino with 2 to 8 carbon atoms, "trialkylsilyl with 3 to 6 carbon atoms, phenyl or phenoxy, each substituent being optionally substituted. phenyl or phenoxy ring and the substituents being independently selected from one to three residues W or one or more radicals R 12, respectively, independently of each other, means a carbocyclic or heterocyclic ring, non-aromatic, with 5 or 6 members , which contains, if appropriate, one or two ring members selected from the group C (= 0), SO or S (= 0) 2, and which may be substituted, if appropriate, by one to four chosen substituents , independently of one another, between alkyl having 1 to 2 carbon atoms, halogen, cyano, nitro or alkoxy with 1 to 2 carbon atoms, or independently, meaning alkenyl with 2 to 6 carbon atoms, alkynyl with 2 to 6 carbon atoms, cycloalkyl with 3 to 7 carbon atoms, (cyano) cycloalkyl with 3 to 7 carbon atoms, (alkyl with 1 to 4 carbon atoms) cycloalkyl with 3 to 6 carbon atoms, (cycloalkyl with 3 a 6 carbon atoms) alkyl with 1 to 4 carbon atoms, pu Where each cycloalkyl, (alkyl) cycloalkyl and (cycloalkyl) -alkyl, if appropriate, are substituted by one or more halogen atoms, J denotes respectively, independently of each other, a heteroaromatic ring with 5 or 6 members, optionally substituted , the substituents can be chosen, independently of each other, between one to three residues W or one or more residues R12, Rs signify, independently of each other, -C (= E1) R19, LC (= E1) R19, -C (= EX ) LR19, -LC ^ E ^ LR19, -OP (= Q) (OR19) 2, -S02LR18 or - LS02LR19, meaning each E1, independently of each other, O, S, N-R15, N-OR15, NN (R15 ) 2, NS = 0, N-CN or N-N02, R7 means hydrogen, alkyl with 1 to 4 carbon atoms, halogenalkyl with 1 to 4 carbon atoms, halogen, alkoxy with 1 to 4 carbon atoms, haloalkoxy with 1 to 4 carbon atoms, alkylthio with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, halogenalkylthio with 1 to 4 carbon atoms, halogenalkylsulfinyl with 1 to 4 carbon atoms, halogenalkylsulfonyl with 1 to 4 carbon atoms, R9 means haloalkyl with 1 to 4 carbon atoms, haloalkoxy with 1 to 4 carbon atoms, haloalkylsulfinyl with 1 to 4 carbon atoms or halogen, R10 means hydrogen, alkyl having 1 to 4 carbon atoms, halogenalkyl having 1 to 4 carbon atoms, halogen, cyano or halogenalkoxy having 1 to 4 carbon atoms, R11 signifies respectively, independently yes, alkylthio having 1 to 6 carbon atoms, alkylsulfenyl having 1 to 6 carbon atoms, halogenoalkylthio having 1 to 6 carbon atoms, halogenoalkylsulfenyl having 1 to 6 carbon atoms, phenylthio or phenylsulfenyl respectively substituted, if appropriate, to three times, the substituents being independently selectable from the list formed by W, -S (0) nN (R16) 2, -C (= 0) R13, -L (C = 0) R14, -S (C = 0) LR14 , -C (= 0) LR13, S (0) nNR13C (= 0) R13, -S (0) nNR13C (= 0) LR14 or -S (O) nNR13S (O) 2LR14, L mean respectively, independently of each other, O, NR18 or S, R12 mean respectively, independently of each other, -B (OR17) 2, amino, SH, thiocyanate, trialkylsilyloxy with 3 to 8 carbon atoms, alkyl disulfide with 1 to 4 carbon atoms, -SF5, -C (= E) R19, -LC (= E) R19, C (= E) LR19, -LC (= E) LR19, -OP (= Q) (OR19) 2, -S02LR19 or -LS02LR19, Q means O or S, R 13 are respectively, independently of one another, hydrogen or mean alkyl having 1 to 6 carbon atoms, alkenyl having 2 to 6 carbon atoms, alkynyl having 2 to 6 carbon atoms or cycloalkyl having 3 to 6 carbon atoms each substituted, if appropriate, one or more times, the substituents being independently selected from R6, halogen, cyano, nitro, hydroxy, alkoxy with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, alkylamino with 1 to 4 carbon atoms, dialkylamino with 2 to 8 carbon atoms, cycloalkylamino with 3 to 6 carbon atoms carbon or (C1-C4 alkyl) cycloalkylamino with 3 to 6 carbon atoms, mean respectively, independently of each other, alkyl with 1 to 20 carbon atoms, alkenyl with 2 to 20 carbon atoms, alkynyl with 2 to 20 carbon atoms or cycloalkyl with 3 to 6 carbon atoms substituted, if appropriate, one or more times, the substituents being independently selected from R 6, halogen, cyano, nitro, hydroxy, alkoxy with 1 to 4. carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, alkylamino with 1 to 4 carbon atoms, dialkylamino with 2 to 8 carbon atoms, cycloalkylamino with 3 to 6 carbon atoms or ( alkyl with 1 to 4 carbon atoms) cycloalkylamino with 3 to 6 carbon atoms or means substituted phenyl, optionally substituents being chosen, independently from one another, from one to three residues W or one or more r these R 12, respectively, independently of each other, mean hydrogen or halogenalkyl with 1 to 6 carbon atoms or alkyl with 1 to 6 carbon atoms, respectively substituted, if appropriate, once or several times, substituents may be chosen independently from each other , between cyano, nitro, hydroxy, alkoxy with 1 to 4 carbon atoms, halogenalkoxy with 1 to 4 carbon atoms, alkylthio with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 atoms of carbon, halogenalkylthio with 1 to 4 carbon atoms, halogenalkylsulfinyl with 1 to 4 carbon atoms, halogenalkylsulfonyl with 1 to 4 carbon atoms, alkylamino with 1 to 4 carbon atoms, dialkylamino with 2 to 8 carbon atoms, alkoxycarbonyl with 2 to 6 carbon atoms, alkylcarbonyl with 2 to 6 carbon atoms, trialkylsilyl with 3 to 6 carbon atoms or phenyl, optionally substituted, substitions may be chosen Examples of these, independently of one another, between one to three residues W or one or more radicals R 12, or N (R 15) 2, mean a ring, which forms the ring M, R 16 means alkyl having 1 to 12 carbon atoms or halogenoalkyl with 1 to 12 carbon atoms, or N (Rle) 2, means a ring, which forms the ring M, R 17 respectively mean, independently of each other, hydrogen or alkyl having 1 to 4 carbon atoms, or B (OR 17) 2 means a ring , wherein both oxygen atoms are linked through a chain with two to three carbon atoms, which may be substituted, if appropriate, by one or two substituents chosen, independently from each other, between methyl or alkoxycarbonyl with 2 to 6 carbon atoms, R18 respectively mean, independently of one another, hydrogen, alkyl having 1 to 6 carbon atoms or halogenalkyl having 1 to 6 carbon atoms, or N (R13) (R18) means a cycle, which forms the M ring, R19 respectively denotes, independently of one another, hydrogen or means alkyl having from 1 to 6 carbon atoms substituted, if appropriate, one or more times, the substituents being independently selectable from cyano, nitro, hydroxy, alkoxy with 1 to 4 carbon atoms, halogenalkoxy with 1 to 4 carbon atoms, alkylthio with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, halogenalkylthio with 1 to 4 carbon atoms , halogenalkylsulfinyl with 1 to 4 carbon atoms, halogenalkylsulfonyl with 1 to 4 carbon atoms, alkylamino with 1 to 4 carbon atoms, dialkylamino with 2 to 8 carbon atoms, C02H, alkoxycarbonyl with 2 to 6 carbon atoms, alkylcarbonyl with 2 to 6 carbon atoms, trialkylsilyl having 3 to 6 carbon atoms or phenyl, optionally substituted, it being possible to choose the substituents, independently from each other, between not three residues W, halogenalkyl with 1 to 6 carbon atoms, cycloalkyl with 3 to 6 carbon atoms or phenyl or pyridyl respectively substituted, if appropriate, one to three times per W, M means a substituted ring respectively, in case given, from one to four times, containing, in addition to the nitrogen atom, with which the pair of substituents R13 and R18, (R15) 2 or (R16) 2, of two to 6 carbon atoms and, in in addition, another nitrogen, sulfur or oxygen atom and the substituents may be chosen, independently of one another, from alkyl having 1 to 2 carbon atoms, halogen, cyano, nitro or alkoxy having 1 to 2 carbon atoms, W respectively mean, independently of each other, alkyl having 1 to 4 carbon atoms, alkenyl with 2 to 4 carbon atoms, alkynyl with 2 to 4 carbon atoms, cycloalkyl with 3 to 6 carbon atoms, halogenoalkyl with 1 to 4 atoms carbon, halogenalkenyl with 2 a 4 carbon atoms, halogenalkynyl with 2 to 4 carbon atoms, halogencycloalkyl with 3 to 6 carbon atoms, halogen, cyano, nitro, alkoxy with 1 to 4 carbon atoms, haloalkoxy with 1 to 4 carbon atoms, alkylthio with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, alkylsulfonyl with 1 to 4 carbon atoms, alkylamino with 1 to 4 carbon atoms, dialkylamino with 2 to 8 carbon atoms, cycloalkylamino with 3 to 6 atoms of carbon, (C 1 -C 4 alkyl) C 3 -C 6 -cycloalkylamino, C 2 -C 4 -alkylcarbon, C 2 -C 6 -alkoxycarbonyl, C02H, C 2 -C 6 alkylaminocarbonyl, dialkylaminocarbonyl with 3 to 8 carbon atoms or trialkylsilyl with 3 to 6 carbon atoms, n mean respectively, independently of each other, 0 or 1, p mean respectively, independently of each other, 0, 1 or 2, being present, in the case where (a) R? means hydrogen, alkyl having 1 to 6 carbon atoms, halogenoalkyl with 1 to 6 carbon atoms, halogenalkenyl with 2 to 6 carbon atoms, halogenoalkynyl with 2 to 6 carbon atoms, halogenalkoxy with 1 to 4 carbon atoms, halogenalkylthio with 1 to 4 carbon atoms or halogen and (b) R8 means hydrogen, alkyl having 1 to 6 carbon atoms, halogenalkyl with 1 to 6 carbon atoms, halogenalkenyl with 2 to 6 carbon atoms, haloalkynyl with 2 to 6 carbon atoms carbon, halogenalkoxy with 1 to 4 carbon atoms, halogenalkylthio with 1 to 4 carbon atoms, halogen, alkylcarbonyl with 2 to 4 carbon atoms, alkoxycarbonyl with 2 to 6 carbon atoms, alkylaminocarbonyl with 2 to 6 carbon atoms or dialkylaminocarbonyl with 3 to 8 carbon atoms, (c) at least one substituent, chosen from Re, R11 and R12 and (d), when R12 is not present, at least one R6 or R11 is different from alkylcarbonyl with 2 to 6 carbon atoms. and carbon, alkoxycarbonyl with 2 to 6 carbon atoms, alkylaminocarbonyl with 2 to 6 carbon atoms and dialkylaminocarbonyl with 3 to 8 carbon atoms and the compounds of the general formula (I) embrace, also, the N-oxides and the salts. and, at least, an active product of the group of pyrethroids (active products of the group) have a synergistic activity and are suitable for the fight against animal pests. 2. Agents according to claim 1, characterized in that they contain, at least, one active product of the group of anthranilic acid amides of the formula d-1), wherein R2 means hydrogen or alkyl having 1 to 6 carbon atoms, R3 means alkyl having 1 to 6 carbon atoms, which is, if appropriate, substituted by R6, R4 means alkyl having 1 to 4 carbon atoms, halogenalkyl with 1 to 2 carbon atoms, halogenalkoxy with 1 to 2 carbon atoms or halogen, R 5 is hydrogen, alkyl having 1 to 4 carbon atoms, halogen with 1 to 2 carbon atoms, halogen with 1 to 2 carbon atoms or halogen, R6 means -C (= E2) R19, -LC (= E2) R19, -C (= E2) LR19 or i -LC (= E2) LR19, meaning each E2, independently of each other O, S, N-R15, N -OR15, NN (R15) 2, and meaning each L, independently of each other, O or NR18, R7 means haloalkyl with 1 to 4 carbon atoms or halogen, R9 means haloalkyl with 1 to 2 carbon atoms, haloalkoxy with 1 to 2 carbon atoms, S (0) p- halogenoalkyl with 1 to 2 carbon atoms or halogen, R15 signifies, independently of one another, hydrogen or, for example, halogenalkyl having 1 to 6 carbon atoms or alkyl having 1 to 6 carbon atoms substituted, optionally, the substituents being independently selected from cyano, alkoxy with 1 to 4 carbon atoms, halogenalkoxy with 1 to 4 carbon atoms, alkylthio with 1 to 4 carbon atoms, alkylsulfinyl with 1 to 4 carbon atoms, 'alkylsulfonyl with 1 to 4 carbon atoms, alkylthio with 1 to 4 carbon atoms carbon, halogenalkylsulfinyl having 1 to 4 carbon atoms or halogenalkylsulfonyl having 1 to 4 carbon atoms, R18 respectively meaning hydrogen or alkyl having 1 to 4 carbon atoms, R19 signifying respectively, independently of each other, hydrogen or alkyl having 1 to 4 carbon atoms; 6 carbon atoms, p mean, independently of each other, 0, 1,

2.

3. Agents according to claim 1 or 2, characterized in that they contain, at least enos, an active product of the group of pyrethroids (active group 2), chosen from (2-1) Acrinathrin and / or (2-2) Alpha-cypermethrin and / or (2-3) Betacyfluthrin and / or (2-4) Cyh alothrin and / or (2-5) Cyp 'ermethrii and / or (2-9) Fenpropath; rin and / or (2-10) Fenvalerat and / or (2-12) Lambda-Cyhalothrin and / or (2-13) Permethrin and / or (2-14) Taufluvalinat and / or (2-15) Tralomethrin and / or [2-16) Zeta-cypermethrin and / or (2-17) Cyf luthrin and / or (2-18) Bifenthrin and / or (2-19) Cycloprothrin and / or (2-20) Eflusilanat R 20 -CrL O "C ° 2CH3 R21 = -CH = CH. Or -CH. -CH2CH3 and / or (2-23) Resmethrin and / or (2-24) Gamma-Cyhalothrin

4. Agents, according to claims 1, 2 or 3, characterized in that they contain anthranilic acid amides of the formula (I) and at least one pyrethroid (group 2) ) in the ratio of 50: 1 to 1:50.

5. Use of a mixture, with synergistic activity, containing compounds of the formula (I), according to claims 1 or 2, and, at least, a pyrethroid (group 2) for the control of animal pests.

6. - Process for obtaining pesticidal agents, characterized in that a mixture is combined, with synergistic activity, containing compounds of the formula (I), according to claims 1 or 2, and, at least, a pyrethroid (group 2) with extender agents and / or surfactants. SUMMARY OF THE INVENTION The invention refers to new combinations of active products, insecticides, which are constituted by anthranilic acid amides, on the one hand and, on the other hand, by other active products, insecticides, chosen from the group of pyrethroids and they are suitable, in a very good way, for the fight against animal pests, such as insects.