US2009074887A1PendingUtilityA1
Fungicidal active compound combinations
Est. expiryApr 28, 2013(expired)· nominal 20-yr term from priority
A01N 37/24A01N 37/22
74
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Claims
Abstract
There are described new active compound combinations of a compound of the formula (I) with known fungicidal active compounds, and their use for the control of phytopathogenic fungi.
Claims
exact text as granted — not AI-modified1 - 3 . (canceled)
4 . A synergistic fungicidal composition comprising synergistic fungicidally effective amounts of the combination of a compound of the formula
and a second compound selected from the group consisting of
(D) propineb of the formula
and/or
(E) tetramethyl-thiuram disulphide of the formula
and/or
(F) mancozeb of the formula
and/or
(G) anilazine of the formula
and/or
(H) copper oxychloride
and/or
(K) a morpholine derivative of the formula
and/or
(L) dithianone of the formula
and/or
(N) cymoxanil of the formula
(P) fosetyl of the formula
or its aluminum adduct
and/or
(O) metalaxyl of the formula
and/or
(R) oxadixyl of the formula
and/or
(U) an azole derivative of the formula
and/or
(V) an azole derivative from the group consisting of
a) difenconazole
b) penconazole
c) flusilazole
d) hexaconazole
e) myclobutanil
f) prochloraz
g) fluquinconazole
h) epoxiconazole
i) fenpropidin
j) perifenox
k) 8-t-butyl-2-(N-ethyl-N-n-propylamino)-methyl-1,4-dioxaspiro[4,5]decane
and/or
(W) metiram
and/or
(X) diethofencarb
and/or
(Y) mephanipyrim and/or
cyprodinyl
and/or
(α) phenylpyrrole
and/or
(β) iprodione
and/or
(Π) vinclozolin
and/or
(ε) benomyl
and/or
(θ) thiphanate and/or
thiophanate-methyl
and/or
(n) compounds of the formula
5 . A composition according to claim 4 , wherein the weight ratio of the compound of the formula (I)
to active compound of the group (D) is between 1:0.5 and 1:50, to active compound of the group (E) is between 1:0.5 and 1:50, to active compound of the group (F) is between 1:0.5 and 1:50, to active compound of the group (G) is between 1:0.5 and 1:50, to active compound of the group (H) is between 1:1 and 1:50, to active compound of the group (K) is between 1:0.1 and 1:10, to active compound of the group (L) is between 1:0.5 and 1:50, to active compound of the group (N) is between 1:0.1 and 1:10, to active compound of the group (P) is between 1:0.1 and 1:20, to active compound of the group (Q) is between 1:0.1 and 1:10, to active compound of the group (R) is between 1:0.1 and 1:10, to active compound of the group (U) is between 1:0.01 and 1:10, to active compound of the group (V) is between 1:0.01 and 1:10, to active compound of the group (W) is between 1:0.5 and 1:50, to active compound of the group (X) is between 1:0.1 and 1:10, to active compound of the group (Y) is between 1:0.1 and 1:10, to active compound of the group (α) is between 1:0.1 and 1:10, to active compound of the group (β) is between 1:0.1 and 1:20, to active compound of the group (Π) is between 1:0.1 and 1:20, to active compound of the group (ε) is between 1:0.1 and 1:10, to active compound of the group (θ) is between 1:0.1 and 1:150, to active compound of the group (n) is between 1:0.025 and 1:10.
6 . A method of combating fungi which comprises administering to such fungi or to a fungus habitat a synergistic fungicidally effective amount of a composition according to claim 4 .
7 . The synergistic fungicidal composition according to claim 4 , wherein the second compound is (β) iprodione or (γ) vinclozolin.
8 . A method of combating fungi which comprises administering to such fungi or to a fungus habitat a synergistic fungicidally effective amount of a composition according to claim 7 .
9 . The synergistic fungicidal composition according to claim 4 , wherein the second compound is (α) phenylpyrrole.
10 . A method of combating fungi which comprises administering to such fungi or to a fungus habitat a synergistic fungicidally effective amount of a composition according to claim 9 .Join the waitlist — get patent alerts
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