Fungicide active substance combinations

Abstract

The novel active compound combinations comprising 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]2,4-dihydro-[1,2,4]-triazole-3-thione of the formula 1

Description

[0001] The present invention relates to novel active compound combinations which consist of the known 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazole-3-thione and further known fungicidally active compounds, and which are highly suitable for controlling phytopathogenic fungi.

[0002] It is already known that 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazole-3-thione has fungicidal properties (cf. WO 96-16 048). The activity of this compound is good, however, at low application rates it is in some cases not satisfactory.

[0003] Furthermore, it is already known that a large number of triazole derivatives aniline derivatives, dicarboximides and other heterocycles can be employed for controlling fungi (cf. EP-A 0 040 345, DE-A 2 201 063, DE-A 2 324 0 10, Pesticide Manual, 9th Edition (1991), paces 249 and 827, U.S. Pat. No. 3,903,090 and EP-A 0 206 999) Likewise, the activity of these compounds is not always satisfactory at loss application rates

[0004] Finally, it is also known that 1-[(6-chloro-3-pyridinyl)-methyl]-N-nitro-2-imidazolidineimine can be used for controlling animal pests such as insects (cf Pesticide Manual, 9th Edition (1991), page 491). However, fungicidal properties have not hitherto been described for this compound.

[0005] It has now been found that the novel active compound combinations comprising

[0006] 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazole-3-thione of the formula 2

[0007] and

[0008] (1) a triazole derivative of the formula 3

[0009] in which

[0010] X represents chlorine or phenyl

[0011] and

[0012] Y represents 4

[0013] and/or

[0014] (2) the triazole derivative of the formula 5

[0015] and/or

[0016] (3) an aniline derivative of the formula 6

[0017] in which

[0018] R1 represents hydrogen or methyl,

[0019] and/or

[0020] (4) N-[1-(4-chloro-phenyl)-ethyl]-2,2-dichloro-1-ethyl-3-methyl-cyclopropane-carboxamide of the formula 7

[0021] and/or

[0022] (5) the zinc propylene-1,2-bis-(dithiocarbamate) of the formula 8

[0023] and/or

[0024] (6) at least one thiocarbamate of the formula 9

[0025] Me=Zn or Mn or a mixture of Zn and Mn

[0026] and/or

[0027] (7) the aniline derivative of the formula 10

[0028] and/or

[0029] (8) the compound of the formula 11

[0030] and/or

[0031] (9) the benzothiadiazole derivative of the formula 12

[0032] and/or

[0033] (10) the 8-t-butyl-2-(N-ethyl-N-n-propyl-amino)-methyl-1,4-dioxaspiro-[5,4]-decane of the formula 13

[0034] and/or

[0035] (11) the compound of the formula 14

[0036] and/or

[0037] (12) the compound of the formula 15

[0038] and/or

[0039] (13) the compound of the formula 16

[0040] and/or

[0041] (14) the dicarboximide of the formula 17

[0042] and/or

[0043] (15) a pyrimidine derivative of the formula 18

[0044] in which

[0045] R2 represents methyl or cyclopropyl,

[0046] and/or

[0047] (16) the phenyl derivative of the formula 19

[0048] and/or

[0049] (17) the morpholine derivative of the formula 20

[0050] and/or

[0051] (18) the phthalimide derivative of the formula 21

[0052] and/or

[0053] (19) the phosphorus compound of the formula 22

[0054] and/or

[0055] (20) a phenylpyrrole derivative of the formula 23

[0056] in which

[0057] R3 and R4 each represent chlorine or together represent a radical of the formula —O—CF2—O—,

[0058] and/or

[0059] (21) the 1-[(6-chloro-3-pyridinyl)-methyl]-N-nitro-2-imidazolidineimine of the formula 24

[0060] and/or

[0061] (22) the phenylurea derivative of the formula 25

[0062] and/or

[0063] (23) the benzamide derivative of the formula 26

[0064] and/or

[0065] (24) a guanidine derivative of the formula 27

[0066] x(2+m)CH3COOH

[0067] in which

[0068] m represents integers from 0 to 5

[0069] and

[0070] R5 represents hydrogen (17 to 23%) or the radical of the formula 28

[0071] (77 to 83%).

[0072] have very good fungicidal properties.

[0073] Surprisingly, the fungicidal activity of the active compound combinations according to the invention is considerably higher than the sum of the activities of the individual active compounds. Thus, an unforeseeable, true synergistic effect is present, and not just an addition of activities.

[0074] The 2-[2-(1-chlorocyclopropyl)-3 (2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazole-3-thione of the formula (I) is known (cf. WO 96-16 048) The compound can be present in the ,,thiono,, form of the formula 29

[0075] or in the tautomeric ,,mercapto,, form of the formula 30

[0076] For simplicity's sake, only the ,,thiono,, form is given in each case.

[0077] The formula (II) includes the compounds

[0078] 1-(4-chloro-phenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butane-2-one of the formula 31

[0079] 1-(4-chloro-phenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-ol of the formula 32

[0080] and

[0081] 1-(4-phenyl-phenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-ol of the formula 33

[0082] The formula (IV) includes the aniline derivatives of the formulae 34

[0083] and

[0084] It is evident from the formula for the active compound of the formula (V) that the compound has three asymmetrically substituted carbon atoms The product may therefore be present as a mixture of various isomers, or else in the form of a single component. Particular preference is given to the compounds

[0085] N-(R)-[1-(4-chloro-phenyl)-ethyl]-(1S)-2,2-dichloro-1-ethyl-3t-methyl-1r-cyclopropanecarboxamide of the formula 35

[0086] and

[0087] N-(R)-[1-(4-chloro-phenyl)-ethyl]-(1R)-2,2-dichloro-1-ethyl-3t-methyl-1r-cyclopropanecarboxamide of the formula 36

[0088] The formula (VII) includes the compounds

[0089] (VIIa) Me=Zn (zineb)

[0090] (VIIb) Me=Mn (maneb)

[0091] and

[0092] (VIIc) mixture of (VIIa) and (VIIb) (mancozeb).

[0093] The formula (XVI) includes the compounds

[0094] (XVIa) R2═CH3 (pyrimethanil)

[0095] and

[0096] (XVIb) R2= 37

[0097] (cyprodinyl)

[0098] The formula (XXI) includes the compounds

[0099] 4-(2,3-dichlorophenyl)-pyrrole-3-carbonitrile of the formula 38

[0100] and

[0101] 4-(2,2-difluoro-1,3-benzodioxol-7-yl)-1H-pyrrole-3-carbonitrile of the formula 39

[0102] The guanidine derivative of the formula (XXV) is a mixture of substances of the common name guazatine.

[0103] The components which are present in the active compound combinations according to the invention in addition to the active compound of the formula (I) are also known Specifically, the active compounds are described in the following publications:

[0104] (1) Compounds of the formula (II)

[0105] DE-A 2 201 063

[0106] DE-A 2 324 010

[0107] (2) Compound of the formula (III)

[0108] EP-A 0 040 345

[0109] (3) Compounds of the formula (IV)

[0110] Pesticide Manual, 9th Edition (1991) pages 249 and 927

[0111] (4) Compound of the formula (V) and individual isomers thereof

[0112] EP-A 0 341 475

[0113] (5) Compound of the formula (VI)

[0114] Pesticide Manual, 9th Edition (1991), page 726

[0115] (6) Compounds of the formula (VII)

[0116] Pesticide Manual, 9th Edition (1991), pages 529, 531 and 866

[0117] (7) Compound of the formula (VIII)

[0118] EP-A 0 339 418

[0119] (8) Compound of the formula (IX)

[0120] EP-A 0 472 996

[0121] (9) Compound of the formula (X)

[0122] EP-A 0 313 512

[0123] (10) Compound of the formula (XI)

[0124] EP-A 0281 842

[0125] (11) Compound of the formula (XII)

[0126] EP-A 0 382 375

[0127] (12) Compound of the formula (XIII)

[0128] EP-A 0 515 901

[0129] (13) Compound of the formula (XIV)

[0130] EP-A 196 02 095

[0131] (14) Compound of the formula (XV)

[0132] U.S. Pat. No. 3,903,090

[0133] (15) Compounds of the formula (XVI)

[0134] EP-A 0 270 111

[0135] EP-A 0 310 550

[0136] (16) Compound of the formula (XVII)

[0137] Pesticide Manual, 9th Edition (1991), page 159

[0138] (17) Compound of the formula (XVIII)

[0139] EP-A 0 219 756

[0140] (18) Compound of the formula (XIX)

[0141] Pesticide Manual, 9th Edition (1991), page 431

[0142] (19) Compound of the formula (XX)

[0143] Pesticide Manual, 9th Edition (1991), page 443

[0144] (20) Compounds of the formula (XXI)

[0145] EP-A 0 236 272

[0146] EP-A 0 206 999

[0147] (21 ) Compound of the formula (XXII)

[0148] Pesticide Manual, 9th Edition (1991), page 491

[0149] (22) Compound of the formula (XXIII)

[0150] DE-A 2 732 257

[0151] (23) Compound of the formula (XXIV)

[0152] EP-A 0 600 629

[0153] (24) Substance of the formula (XXV)

[0154] Pesticide Manual, 9th Edition (1991), page 461

[0155] In addition to the active compound of the formula (I), the active compound combinations according to the invention comprise at least one active compound of the compounds of groups (1) to (24). Additionally, they may comprise further fungicidally active components.

[0156] The synergistic effect is particularly pronounced when the active compounds in the active compound combinations according to the invention are present in certain weight ratios. However, the weight ratios of the active compounds in the active compound combinations can be varied within a relatively Wide range. In general,

[0157] 0.1 to 20 parts by weight, preferably 0.2 to 10 parts by weight, of active compound of group (1),

[0158] 0.1 to 20 parts by weight, preferably 0.2 to 10 parts by weight, of active compound of group (2),

[0159] 0.2 to 150 parts by weight, preferably 1 to 100 parts by weight, of active compound of group (3),

[0160] 0.1 to 10 parts by weight, preferably 0.2 to 5 parts by weight, of active compound of group (4),

[0161] 1 to 50 parts by weight, preferably 5 to 20 parts by weight, of active compound of group (5),

[0162] 1 to 50 parts by weight, preferably 2 to 20 parts by weight, of active compound of group (6),

[0163] 0.1 to 50 parts by weight, preferably 1 to 30 parts by weight, of active compound of group (7),

[0164] 0.2 to 50 parts by weight, preferably 1 to 20 parts by weight, of active compound of group (8),

[0165] 0.02 to 50 parts by weight, preferably 0.2 to 10 parts by weight, of active compound of group (9),

[0166] 0.1 to 50 parts by weight, preferably 0.2 to 20 parts by weight, of active compound of group (10),

[0167] 0.1 to 50 parts by weight, preferably 0.2 to 20 parts by weight, of active compound of group (11),

[0168] 0.1 to 50 parts by weight, preferably 0.2 to 20 parts by weight, of active compound of group (12),

[0169] 0.1 to 50 parts by weight, preferably 0.2 to 20 parts by weight, of active compound of group (13)

[0170] 0.1 to 50 parts by weight, preferably 1 to 30 parts by weight, of active compound of group (14),

[0171] 0.1 to 50 parts by weight, preferably 0.2 to 20 parts by weight, of active compound of group (15),

[0172] 0.1 to 50 parts by weight, preferably 2 to 20 parts by weight, of active compound of group (16),

[0173] 1 to 20 parts by weight, preferably 2 to 10 parts by weight, of active compound of group (17),

[0174] 1 to 50 parts by weight, preferably 2 to 20 parts by weight, of active compound of group (18),

[0175] 1 to 50 parts by weight, preferably 2 to 20 parts by weight, of active compound of group (19),

[0176] 0.1 to 10 parts by weight, preferably 0.2 to 5 parts by weight, of active compound of group (20),

[0177] 0.05 to 20 parts by weight, preferably 0.1 to 10 parts by weight, of active compound of group (21),

[0178] 0.1 to 10 parts by weight, preferably 0.2 to 5 parts by weight, of active compound of group (22),

[0179] 0.1 to 10 parts by weight, preferably 0.2 to 5 parts by weight, of active compound of group (23),

[0180] and/or

[0181] 0.1 to 10 parts by weight, preferably 0.2 to 5 parts by weight, of active compound of group (24)

[0182] are present per part by weight of active compound of the formula (I)

[0183] The active compound combinations according to the invention have very good fungicidal properties and can be employed for controlling phytopathogenic fungi, such as Plasmodiophoromycetes, Oomycetes, Chytridiomycetes, Zygomycetes, Ascomycetes, Basidiomycetes, Deuteromycetes, etc.

[0184] The active compound combinations according to the invention are particularly suitable for controlling cereal diseases, such as Erysiphe, Puccinia and Fusarium, and for controlling diseases encountered in viticulture, such as Uncinula, Plasmopara and Botrytis, and furthermore in dicotylendonous crops for controlling powdery, and downy mildew fungi and causative organisms of leaf spot

[0185] The fact that the active compound combinations are well tolerated by plants at the concentrations required for controlling plant diseases permits the treatment of above-ground parts of plants, of propagation stock and seeds, and of the soil. The active compound combinations according to the invention can be employed for foliar application or else as seed dressings.

[0186] The active compound combinations according to the invention can be converted to the customary formulations, such as solutions, emulsions, suspensions, powders, foams, pastes, granules, aerosols and microencapsulations in polymeric substances and in coating compositions for seeds, and ULV formulations.

[0187] These formulations are produced in a known manner, for example by mixing the active compounds or active compound combinations with extenders, that is liquid solvents, liquefied gases under pressure, and/or solid carriers, optionally with the use of surfactants, that is emulsifiers and/or dispersants, and/or foam formers. If the extender used is water, it is also possible to use, for example, organic solvents as auxiliary solvents. Essentially, suitable liquid solvents include: aromatics such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics or chlorinated aliphatic hydrocarbons such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons such as cyclohexane or paraffins, for example petroleum fractions, alcohols such as butanol or glycol and their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethylformamide and dimethyl sulphoxide, or else water. Liquefied gaseous extenders or carriers are to be understood as meaning liquids which are gaseous at ambient temperature and under atmospheric pressure, for example aerosol propellants such as butane, propane, nitrogen and carbon dioxide. Suitable solid carriers are: for example ground natural minerals such as kaolins, clays, talc, chalk, quartz, attapulgite, monitmorillonite or diatomaceous earth, and ground synthetic minerals such as finely divided silica, alumina and silicates. Suitable solid carriers for (granules are: for example crushed and fractionated natural rocks such as calcite, marble, pumice, sepiolite and dolomite, or else synthetic granules of inorganic and organic meals, and granules of organic material such as sawdust, coconut shells, maize cobs and tobacco stalks. Suitable emulsifiers and/or foam formers are for example nonionic and anionic emulsifiers, such as polyoxyethylene fatty acid esters, polyoxyetlhylene fatty alcohol ethers, for example alkylaryl polyglycol ethers, alkyl-sulphonates, alkyl sulphates, arylsulphonates, or else protein hydrolysates. Suitable dispersants are: for example lignin-sulphite waste liquors and methylcellulose.

[0188] Tackifiers such as carboxymethylcellulose and natural and synthetic polymers in the form of powders, granules or latices, such as gum arabic, polyvinyl alcohol and polyvinyl acetate, or else natural phospholipids such as cephalins and lecithins and synthetic phospholipids can be used in the formulations. Other additives can be mineral and vegetable oils.

[0189] It is possible to use colorants such as inorganic pigments, for example iron oxide, titanium oxide and prussian blue, and organic dyestuffs such as alizarin dyestuffs, azo dyestuffs and metal phthalocyanine dyestuffs, and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.

[0190] The formulations generally comprise between 0.1 and 95% by weight of active compounds, preferably between 0.5 and 90%

[0191] In the formulations, the active compound combinations according to the invention can be present as a mixture with other known active compounds such as fungicides, insecticides, acaricides and herbicides, and as mixtures with fertilizers or plant (growth regulators.

[0192] The active compound combinations can be used as such, in the form of their formulations or as the use forms prepared therefrom, such as ready-to-use solutions, emulsifiable concentrates, emulsions, suspensions, wettable powders, soluble powders and granules They are used in the customary manner, for example by watering, spraying, atomizing, scattering, spreading, and as a powder for dry seed treatment, a solution for seed treatment, a water-soluble powder for seed treatment, a water-soluble powder for slurry treatment, or by encrusting.

[0193] When using the active compound combinations according to the invention, the application rates can be varied within a relatively wide range, depending on the kind of application. In the treatment of parts of plants, the application rates of the active compound combination are (generally between 0.1 and 10,000 g/ha, preferably between 10 and 1000 g/ha. In the treatment of seeds, the application rates of the active compound combination are generally between 0.001 and 50 g per kilogram of seed, preferably between 0.01 and 10 g per kilogram of seed. In the treatment of the soil, the application rates of the active compound combination are Generally between 0.1 and 10,000 (g/ha, preferably between 1 and 5000 (g/ha.

[0194] The good fungicidal activity of the active compound combinations according to the invention is evident from the examples below. While the individual active compounds exhibit weaknesses with regard to the fungicidal activity, the combinations have an activity which exceeds a simple addition of activities.

[0195] A synergistic effect of fungicides is always present when the fungicidal activity of the active compound combinations exceeds the total of the activities of the active compounds when applied individually.

[0196] The expected activity for a given combination of two active compounds can be calculated as follows (cf. Colby, S. R., “Calculating Synergistic and Antagonistic Responses of Herbicide Combinations”, Weeds 15, (1967), 20-22).

[0197] If

[0198] X is the efficacy when applying active compound A at an application rate of m g/ha,

[0199] Y is the efficacy when applying active compound B at an application rate of n g/ha and

[0200] E is the efficacy when applying the active compounds A and B at an application rate of m and n g/ha,

[0201] then 1$E=X+Y-\frac{X·Y}{100}$

[0202] The efficacy is calculated in %. 0% is an efficacy which corresponds to that of the control, whereas an efficacy of 100% means that no infection is observed.

[0203] If the actual fungicidal activity exceeds the calculated value, then the activity of the combination is superadditive, i.e. a synergistic effect exists. In this case, the efficacy which was actually observed must be greater than the value for the expected efficacy (E) calculated from the abovementioned formula.

[0204] The examples that follow illustrate the invention.

EXAMPLE 1

[0205] Sphaerotheca Test (Cucumber)/Protective

Solvent:    47 parts by weight of acetone
Emulsifier: 3 parts by weight of alkylaryl polyglycol ether

[0206] To produce a suitable preparation of active compound, 1 part by weight of active compound or active compound combination is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration, or a commercial formulation of active compound or active compound combination is diluted with water to the desired concentration.

[0207] To test for protective activity, young plants are sprayed with the active compound preparation at the stated application rate. After the spray coating has dried on, the plants are inoculated with an aqueous spore suspension of Sphaerotheca fuliginea The plants are then placed in a greenhouse at about 23° C. and a relative atmospheric humidity of about 70%.

[0208] Evaluation is carried out 10 days after the inoculation. 0% means an efficacy which corresponds to that of the control, whereas an efficacy of 100% means that no infection is observed.

[0209] Active compounds, application rates and test results are shown in the table below.

TABLE 1
Sphaerotheca test (cucumber)/protective
	Active
	compound
	application rate
Active compound	in g/ha	Efficacy in %
Known:
40	2.5  0.5	21 0
41	25	0
42	25	0
43	25	0
44	25	0
45	25	0
46	50	0
47	25	0
48	25	0
49	25	0
50	12.5	0
51	12.5	0
52	12.5	0
53	12.5	0
54	12.5	0
55	2.5	57
56	2.5	59
57	12.5	15
58	2.5	0
59	2.5	50
60	2.5
61	2.5	80
62	2.5	22
63	2.5	0
According to the invention:		found	calc *)
64	65	70	21
66	67	63	21
68	69	63	21
70	71	63	21
72	73	59	21
74	75	52	21
76	77	63	21
78	79	59	21
80	81	52	21
82	83	50	21
84	85	63	21
86	87	50	21
88	89	75	21
90	91	54	21
92	93	80	57
94	95	75	59
96	97	66	31
98	99	90	21
100	101	85	61
102	103	90	50
104	105	93	84
106	107	70	38
108	109	52	21
found = efficacy found
calc. = efficacy calculated using the Colby formula

EXAMPLE 2

[0210] Venturia Test (Apple)/Protective

Solvent:    47 parts by weight of acetone
Emulsifier: 3 parts by weight of alkylaryl polyglycol ether

[0211] To produce a suitable preparation of active compound, 1 part by weight of active compound or active compound combination is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration, or a commercial formulation of active compound or active compound combination is diluted with water to the desired concentration.

[0212] To test for protective activity, young plants are sprayed with the active compound preparation at the stated application rate. After the spray coating has dried on, the plants are inoculated with an aqueous konidia suspension of the causative organism of apple scab Venturia inaequalis and then remain in an incubation cabin at about 20° C. and 100% relative atmospheric humidity for one day.

[0213] The plants are then placed in a greenhouse at about 21° C. and a relative atmospheric humidity of about 90%.

[0214] Evaluation is carried out 12 days after the inoculation. 0% means an efficacy which corresponds to that of the control, whereas an efficacy of 100% means that no infection is observed.

[0215] Active compounds, application rates and test results are shown in the table below.

TABLE 2
Venturia test (apple)/protective
	Active
	compound
	application rate
Active compound	in g/ha	Efficacy in %
Known:
110	1	1
111	1	0
According to the invention:		found	calc. *)
112	113	54	1
found = efficacy found
calc. = efficacy calculated using the Colby formula

EXAMPLE 3

Erysiphe Test (Barley)/Curative

[0216]

Solvent:    10 parts by weight of N-methyl-pyrrolidone
Emulsifier: 0.6 parts by weight of alkylaryl polyglycol ether

[0217] To produce a suitable preparation of active compound, 1 part by weight of active compound or active compound combination is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration, or a commercial formulation of active compound or active compound combination is diluted with water to the desired concentration.

[0218] To test for curative activity, young plants are dusted with spores of Erysiphe graminis f.sp. hordei. 48 hours after the inoculation, the plants are sprayed with the active compound preparation at the stated application rate.

[0219] The plants are placed in a greenhouse at a temperature of about 20° C. and a relative atmospheric humidity of about 80% to promote the development of mildew pustules.

[0220] Evaluation is carried out 7 days after the inoculation. 0% means an efficacy which corresponds to that of the control, whereas an efficacy of 100% means that no infection is observed.

[0221] Active compounds, application rates and test results are shown in the table below.

TABLE 3
Erysiphe test (barley)/curative
	Active
	compound
	application rate
Active compound	in g/ha	Efficacy in %
Known:
114	25	81
115	25	75
According to the invention:
116	117	100

EXAMPLE 4

Erysiphe Test (Barley)/Protective

[0222]

Solvent:    10 parts by weight of N-methyl-pyrrolidone
Emulsifier: 0.6 parts by weight of alkylaryl polyglycol ether

[0223] To produce a suitable preparation of active compound, 1 part by weight of active compound or active compound combination is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration, or a commercial formulation of active compound or active compound combination is diluted with water to the desired concentration.

[0224] To test for protective activity, young plants are sprayed with the active compound preparation at the stated application rate.

[0225] After the spray coating has dried on, the plants are dusted with spores of Erysiphe graminis f.sp. hordei.

[0226] The plants are placed in a greenhouse at a temperature of about 20° C. and a relative atmospheric humidity of about 80% to promote the development of mildew pustules.

[0227] Evaluation is carried out 7 days after the inoculation. 0% means an efficacy which corresponds to that of the control, whereas an efficacy of 100% means that no infection is observed.

[0228] Active compounds, application rates and test results are shown in the table below

TABLE 4
Erysiphe test (barley)/protective
	Active
	compound
	application rate
Active compound	in g/ha	Efficacy in %
Known:
118	25	83
119	25	92
According to the invention:
120	121	100
122	123	100
124	125	100

EXAMPLE 5

[0229]

Solvent:    10 parts by weight of N-methyl-pyrrolidone
Emulsifier: 0.6 parts by weight of alkylaryl polyglycol ether

[0230] To produce a suitable preparation of active compound, 1 part by weight of active compound or active compound combination is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration, or a commercial formulation of active compound or active compound combination is diluted with water to the desired concentration.

[0231] To test for curative activity, young plants are dusted with spores of Erysiphe graminis f.sp. tritici. 48 hours after the inoculation, the plants are sprayed with the active compound preparation at the stated application rate.

[0232] The plants are then placed in a greenhouse at a temperature of about 20° C. and a relative atmospheric humidity of about 80% to promote the development of mildew pustules.

[0233] Evaluation is carried out 7 days after the inoculation. 0% means an efficacy which corresponds to that of the control, whereas an efficacy of 100% means that no infection is observed.

[0234] Active compounds, application rates and test results are shown in the table below.

TABLE 5
Erysiphe test (wheat)/curative
	Active
	compound
	application rate
Active compound	in g/ha	Efficacy in %
Known:
126	25 12.5  6.25	75 50 25
127	25	88
128	25	81
129	12.5	0
130	12.5	0
131	12.5	0
132	6.25	38
133	6.25	94
According to the invention:
	134	100
135
136	137	100
138	139	100
140	141	100
142	143	100
144	145	63
146	147	75
148	149	100
150	151	100
152	153	100
154	155	75
156	157	50
158	159	100
160	161	100

EXAMPLE 6

[0235] Erysiphe Test (Wheat)/Protective

Solvent:    10 parts by weight of N-methyl-pyrrolidone
Emulsifier: 0.6 parts by weight of alkylaryl polyglycol ether

[0236] To produce a suitable preparation of active compound, 1 part by weight of active compound or active compound combination is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration, or a commercial formulation of active compound or active compound combination is diluted with water to the desired concentration.

[0237] To test for protective activity, young plants are sprayed with the active compound preparation at the stated application rate.

[0238] After the spray coating has dried on, the plants are dusted with spores of Erysiphe graminis f.sp. tritici.

[0239] The plants are then placed in a greenhouse at a temperature of about 20° C. and a relative atmospheric humidity of about 80% to promote the development of mildew pustules.

[0240] Evaluation is carried out 7 days after the inoculation. 0% means an efficacy which corresponds to that of the control, whereas an efficacy of 100% means that no infection is observed.

[0241] Active compounds, application rates and test results are shown in the table below.

TABLE 6
Erysiphe test (wheat)/protective
	Active
	compound	Effi-
	application	cacy
Active compound	rate in g/ha	in %
Known:
162	6.25	57
163	6.25	57
According to the invention:
164	165	79
166	167	71
168	169	71

EXAMPLE 7

[0242] Leptosphaeria nodorum Test (Wheat)/Protective

Solvent:    10 parts by weight of N-methyl-pyrrolidone
Emulsifier: 0.6 parts by weight of alkylaryl polyglycol ether

[0243] To produce a suitable preparation of active compound, 1 part by weight of active compound or active compound combination is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration, or a commercial formulation of active compound or active compound combination is diluted with water to the desired concentration.

[0244] To test for protective activity, young plants are sprayed with the active compound preparation at the stated application rate.

[0245] After the spray coating has dried on, the plants are sprayed with a spore suspension of Leptosphaeria nodorum. The plants remain in an incubation cabin at 20° C. and 100% relative atmospheric humidity for 48 hours.

[0246] The plants are then placed in a greenhouse at a temperature of about 15° C. and a relative atmospheric humidity of about 80%.

[0247] Evaluation is carried out 10 days after the inoculation. 0% means an efficacy which corresponds to that of the control, whereas an efficacy of 100% means that no infection is observed.

[0248] Active compounds, application rates and test results are shown in the table below.

TABLE 7
Leptosphaeria nodorum test (wheat)/protective
	Active
	compound
	application rate
Active compound	in g/ha	Efficacy in %
Known:
170	25	62
171	25	87
According to the invention:
172	173	100

EXAMPLE 8

[0249] Puccinia Test (Wheat)/Protective

Solvent:    10 parts by weight of N-methyl-pyrrolidone
Emulsifier: 0.6 parts by weight of alkylaryl polyglycol ether

[0250] To produce a suitable preparation of active compound, 1 part by weight of active compound or active compound combination is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration, or a commercial formulation of active compound or active compound combination is diluted with water to the desired concentration.

[0251] To test for protective activity, young plants are inoculated with a spore suspension of Puccinia recondita in a 0.1% strength aqueous agar solution. After the spray coating had dried on, the plants are sprayed with the active compound preparation at the stated application rate.

[0252] The plants remain in an incubation cabin at 20° C. and 100% relative atmospheric humidity for 24 hours.

[0253] The plants are then placed in a greenhouse at a temperature of about 20° C. and a relative atmospheric humidity of about 80% to promote the development of rust pustules.

[0254] Evaluation is carried out 10 days after the inoculation 0% means an efficacy which corresponds to that of the control, whereas an efficacy of 100% means that no infection is observed.

[0255] Active compounds, application rates and test results are shown in the table below.

TABLE 8
Puccinia test (wheat)/protective
	Active
	compound
	application rate
Active compound	in g/ha	Efficacy in %
Known:
174	25	38
175	25	94
According to the invention:
176	177	100
178	179	100

EXAMPLE 9

[0256] Fusarium culmorum Test (Wheat)/Seed Treatment

[0257] The active compounds are applied as a dry seed dressing. This is prepared by extending the respective active compound or the active compound combination with ground minerals to give a finely pulverulent mixture which ensures uniform distribution on the seed surface.

[0258] To dress the seed, the infected seed together with the seed dressing is shaken for 3 minutes in a sealed glass flask.

[0259] 2×100 corns of wheat are sown at a depth of 1 cm in standard soil and cultivated in a greenhouse at a temperature of about 18° C. and a relative atmospheric humidity of about 95% in seed trays which receive a light regimen of 15 hours per day.

[0260] About 3 weeks after sowing, the plants are evaluated for symptoms. 0% means an efficacy which corresponds to that of the control, whereas an efficacy of 100% means that no infection is observed.

[0261] Active compounds, application rates and test results are shown in the table below.

TABLE 9
Fusarium culmorum test (wheat)/seed treatment
	Active
	compound
	application rate
Active compound	in g/ha	Efficacy in %
Known:
180	75	32
181	75	27
According to the invention:
182	183	41

EXAMPLE 10

[0262] Fusarium nivale Test (Triticale)/Seed Treatment

[0263] The active compounds are applied as a dry seed dressing. This is prepared by extending the respective active compound or the active compound combination with ground minerals to give a finely pulverulent mixture which ensures uniform distribution on the seed surface.

[0264] To dress the seed, the infected seed together with the seed dressing is shaken for 3 minutes in a sealed glass flask.

[0265] 2×100 corns of wheat are sown at a depth of 1 cm in standard soil and cultivated in a greenhouse at a temperature of about 10° C. and a relative atmospheric humidity of about 95% in seed trays which receive a light regimen of 15 hours per day.

[0266] About 3 weeks after sowing, the plants are evaluated for symptoms. 0% means an efficacy which corresponds to that of the control, whereas an efficacy of 100% means that no infection is observed.

[0267] Active compounds, application rates and test results are shown in the table below

TABLE 10
Fusarium nivale test (triticale)/seed treatment
	Active
	compound
	application rate
Active compound	in g/ha	Efficacy in %
Known:
184	75 25	14 0
185	75	94
186	25	0
According to the invention:
187	188	99
189	190	31

EXAMPLE 11

[0268] Rhizoctonia solani Test (Cotton)/Seed Treatment

[0269] The active compounds are applied as a dry seed dressing. This is prepared by extending the respective active compound or the active compound combination with ground minerals to give a finely pulverulent mixture which ensures uniform distribution on the seed surface.

[0270] To dress the seed, the infected seed together with the seed dressing is shaken for 3 minutes in a sealed glass flask.

[0271] 2×50 corns of seed are sown at a depth of 2 cm in standard soil infected with Rhizoctonia solani, and the seeds are cultivated in a greenhouse at a temperature of about 22° C. in seed trays which receive a light regimen of 15 hours per day.

[0272] Evaluation is carried out after 8 days. 0% means an efficacy which corresponds to that of the control, whereas an efficacy of 100% means that no infection is observed.

[0273] Active compounds, application rates and test results are shown in the table below

TABLE 11
Rhizoctonia solani test (cotton)/seed treatment
	Active compound
	application rate
Active compound	in g/ha	Efficacy in %
Known:
191	(I)	25	19
192	(III)	25	27
193	(IIc)	25	0
According to the invention
194		195	40
196		197	31

Claims

1. Fungicidal compositions, characterized in that they contain an active compound combination consisting of 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazole-3-thione of the formula 198and (1) a triazole derivative of the formula 199in which X represents chlorine or phenyl and Y represents 200and/or (2) the triazole derivative of the formula 201and/or (3) an aniline derivative of the formula 202in which R1 represents hydrogen or methyl, and/or (4) N-[1-(4-chloro-phenyl)-ethyl]-2,2-dichloro-1-ethyl-3-methyl-cyclopropane-carboxamide of the formula 203and/or (5) the zinc propylene-1,2-bis-(dithiocarbamate) of the formula 204n>=1 (propineb) and/or (6) at least one thiocarbamate of the formula 205Me=Zn or Mn or a mixture of Zn and Mn and/or (7) the aniline derivative of the formula 206and/or (8) the compound of the formula 207and/or (9) the benzothiadiazole derivative of the formula 208and/or (10) the 8-t-butyl-2-(N-ethyl-N-n-propyl-amino)-methyl-1,4-dioxaspiro-[5,4]-decane 209and/or (11) the compound of the formula 210and/or (12) the compound of the formula 211and/or (13) the compound of the formula 212and/or (14) the dicarboximide of the formula 213and/or (15) a pyrimidine derivative of the formula 214in which, R2 represents methyl or cyclopropyl, and/or (16) the phenyl derivative of the formula 215and/or (17) the morpholine derivative of the formula 216and/or (18) the phthalimide derivative of the formula 217and/or (19) the phosphorus compound of the formula 218and/or (20) a phenylpyrrole derivative of the formula 219in which R3 and R4 each represent chlorine or together represent a radical of the formula —O—CF2—O—, and/or (21) the 1-[(6-chloro-3-pyridinyl)-methyl]-N-nitro-2-imidazolidineimine of the formula 220and/or (22) the phenylurea derivative of the formula 221and/or (23) the benzamide derivative of the formula 222and/or (24) a guanidine derivative of the formula 223in which m represents integers from 0 to 5 and R5 represents hydrogen (17 to 23%) or the radical of the formula 224(77 to 83%)

2. Composition according to claim 1, characterized in that in the active compound combinations the weight ratio of active compound of the formula (I) to active compound of group (1) is between 1:0.1 and 1:20, active compound of group (2) is between 1:0.1 and 1:20, active compound of group (3) is between 1:0.2 and 1:150, active compound of group (4) is between 1:0.1 and 1:10, active compound of group (5) is between 1:1 and 1:50, active compound of group (6) is between 1:1 and 1:50, active compound of group (7) is between 1:0.1 and 1:50, active compound of group (8) is between 1:0.2 and 1:50, active compound of group (9) is between 1:0.02 and 1:50, active compound of group (10) is between 1:0.1 and 1:50, active compound of group (11) is between 1:0.1 and 1:50, active compound of group (12) is between 1:0.1 and 1:50, active compound of group (13) is between 1:0.1 and 1:50, active compound of group (14) is between 1:0.1 and 1:50, active compound of group (15) is between 1:0.1 and 1:50, active compound of group (16) is between 1:1 and 1:50, active compound of group (17) is between 1:1 and 1:20, active compound of group (18) is between 1:1 and 1:50, active compound of group (19) is between 1:1 and 1:50, active compound of group (20) is between 1:0.1 and 1:10, active compound of group (21) is between 1:0.05 and 1:20, active compound of group (22) is between 1:0.1 and 1:10, active compound of group (23) is between 1:0.1 and 1:10 and active compound of group (24) is between 1:0.1 and 1:10.

3. Method, for controlling fungi, characterized in that active compound combinations according to claim 1 are applied to the fungi and/or their habitat.

4. Use of active compound combinations according to claim 1 for controlling fungi.

5. Process for preparing fungicidal compositions characterized in that active compound combinations according to claim 1 are mixed with extenders and/or surfactants.