US2002173529A1PendingUtilityA1
Fungicide active substance combinations
Priority: Apr 18, 1997Filed: Apr 26, 2001Published: Nov 21, 2002
Est. expiryApr 18, 2017(expired)· nominal 20-yr term from priority
A01N 37/38A01N 51/00A01N 43/84A01N 43/30A01N 47/14A01N 47/04A01N 53/00A01N 47/10A01N 43/653A01N 43/36A01N 37/24A01N 43/88A01N 37/22A01N 57/12A01N 43/54A01N 47/12A01N 37/34A01N 55/02A01N 37/50A01N 43/38A01N 47/32A01N 43/82A01N 37/18A01N 37/20
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Claims
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 and the active compound of groups (1) to (24) listed in the description have very good fungicidal properties.
Claims
exact text as granted — not AI-modified1 . 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 and (1) a triazole derivative of the formula in which X represents chlorine or phenyl and Y represents and/or (2) the triazole derivative of the formula and/or (3) an aniline derivative of the formula in which R 1 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 and/or (5) the zinc propylene-1,2-bis-(dithiocarbamate) of the formula n>=1 (propineb) and/or (6) at least one thiocarbamate of the formula Me=Zn or Mn or a mixture of Zn and Mn and/or (7) the aniline derivative of the formula and/or (8) the compound of the formula and/or (9) the benzothiadiazole derivative of the formula and/or (10) the 8-t-butyl-2-(N-ethyl-N-n-propyl-amino)-methyl-1,4-dioxaspiro-[5,4]-decane and/or (11) the compound of the formula and/or (12) the compound of the formula and/or (13) the compound of the formula and/or (14) the dicarboximide of the formula and/or (15) a pyrimidine derivative of the formula in which, R 2 represents methyl or cyclopropyl, and/or (16) the phenyl derivative of the formula and/or (17) the morpholine derivative of the formula and/or (18) the phthalimide derivative of the formula and/or (19) the phosphorus compound of the formula and/or (20) a phenylpyrrole derivative of the formula in which R 3 and R 4 each represent chlorine or together represent a radical of the formula —O—CF 2 —O—, and/or (21) the 1-[(6-chloro-3-pyridinyl)-methyl]-N-nitro-2-imidazolidineimine of the formula and/or (22) the phenylurea derivative of the formula and/or (23) the benzamide derivative of the formula and/or (24) a guanidine derivative of the formula in which m represents integers from 0 to 5 and R 5 represents hydrogen (17 to 23%) or the radical of the formula (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.Join the waitlist — get patent alerts
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