EP0068296A1
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EP
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A new fungicidal composition, processes for its production and its use
Assignee: A Natterman und Cie GmbH
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Filing: 1982-06-16
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Granted: —
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Expires: 2002-06-16
Abstract
Abstract The invention relates to new fungicidal compositions consisting of one or more fungicidally active ingredients and one or more certain phospholipides in addition to standard vehicles, diluents, solvents and/or other inert auxiliaries, the ratio by weight of fungicidally substances to pure phospholipide or the mixture of pure phospholipides amounting to between 1 : 0.2 and 1 : 20. The invention also relates to processes for controlling fungal diseases using these compositions and to processes for their production.
Inventors
- 👤 Miklos Dipl.-Chem. Dr. Ghyczy
- 👤 Heinrich Dr. Osthoff
- 👤 Eugen Dr. Etschenberg
Bibliographic Details
Application Number
—
Jurisdiction
EP
Data Source
google_patents
Last Synchronized
2026-11-03 16:23
CPC Classifications
A; A01; A01N; A01N57/00; A01N57/10; A01N57/12
Claims Analysis
Total Claims: 20
Claim 1
Independent Claim
68 words
A fungicidal composition, characterised in that it consists of a) one or more fungicidally active substances and b) one or more phospholipides from the group comprising phosphatidyl choline, hydrogenated phosphatidyl cholines, phosphatidyl ethanolamine, N-acyl phosphatidyl ethanolamines, phosphatidyl inositol, phosphatidyl serine, lysolecithin and phosphatidyl glycerol in a ratio by weight of a:b of from 1:0.2 to 1:20 in addition to standard vehicles, diluents, solvents, propellents and/or other inert auxiliaries.
Claim 2
Dependent Claim
68 words
A fungicidal composition, characterised in that it consists of a) one or more fungicidally active substances and b) one or more phospholipides from the group comprising phosphatidyl choline, hydrogenated phosphatidyl cholines, phosphatidyl ethanolamine, N-acyl phosphatidyl ethanolamines, phosphatidyl inositol, phosphatidyl serine, lysolecithin and phosphatidyl glycerol in a ratio by weight of a:b of from 1:0.2 to 1:20 in addition to standard vehicles, diluents, solvents, propellents and/or other inert auxiliaries.
Claim 3
Dependent Claim
27 words
A fungicidal composition as claimed in Claim 1, characterised in that constituents a) and b) are present in a ratio by weight of from 1:0.5 to 1:10.
Claim 4
Dependent Claim
29 words
A fungicidal composition as claimed in Claim 1 or 2, characterised in that constituents a) and b) are present in a ratio by weight of from 1:1 to 1:5.
Claim 5
Dependent Claim
24 words
A fungicidal composition as claimed in one or more of Claims 1 to 3, characterised in that phosphatidyl choline is used as the phospholipide.
Claim 6
Dependent Claim
111 words
A fungicidal composition as claimed in one or more of Claims 1 to 4, characterised in that one or more compounds from the following groups is/are used as the fungicidally active substance: 1. aromatic nitro compounds corresponding to the following general formula in which R 1 represents C 2 -C 4 -alkenyl or branched alkoxy and R 2 represents C 2 -C 6 -alkyl; 2. ehlorobenzenes corresponding to the following general formula in which R 1 represents Cl or H, R 2 represents Cl, -OCH 3 or H, R 3 represents Cl or -CN, R 4 represents Cl or H and R 5 represents -CN,-OCH 3 or - N0 2 ;
Claim 7
Dependent Claim
19 words
phthalic acid derivatives corresponding to the following general formula in which R represents an alkylthio, haloalkyl or thionophosphoryl group;
Claim 8
Dependent Claim
19 words
phthalic acid derivatives corresponding to the following general formula in which R represents an alkylthio, haloalkyl or thionophosphoryl group;
Claim 9
Dependent Claim
3 words
fungicidally active thiocarbamates;
Claim 10
Dependent Claim
3 words
fungicidally active thiocarbamates;
Claim 11
Dependent Claim
3 words
fungicidally active benzimidazoles;
Claim 12
Dependent Claim
3 words
fungicidally active benzimidazoles;
Claim 13
Dependent Claim
4 words
fungicidally active aniline derivatives;
Claim 14
Dependent Claim
4 words
fungicidally active aniline derivatives;
Claim 15
Dependent Claim
25 words
such fungicides as thiophanat, dodemorph, tridemorph, anilazin, bupirimat, cetactaelat, chinomethionat, chlormethionat, dichlorfluanid, dimethirimol, dithianon, dodin, ethirimol, fenaminsulf, fenarimol, iprodion, pyrazophos, tolylfluanid, triadimefon, triadimenol, triflorin, vinclozolin.
Claim 16
Dependent Claim
25 words
such fungicides as thiophanat, dodemorph, tridemorph, anilazin, bupirimat, cetactaelat, chinomethionat, chlormethionat, dichlorfluanid, dimethirimol, dithianon, dodin, ethirimol, fenaminsulf, fenarimol, iprodion, pyrazophos, tolylfluanid, triadimefon, triadimenol, triflorin, vinclozolin.
Claim 17
Dependent Claim
19 words
The use of the fungicidal compositions claimed in one or more of Claims 1 to 5 for controlling fungi.
Claim 18
Dependent Claim
78 words
A process for producing the fungicidal compositions claimed in one or more of Claims 1 to 5, characterised in that the phospholipide is dissolved in an organic solvent or in a mixture of organic solvents and the fungicide is dissolved in the resulting solution, optionally by heating and/or stirring, after which the solvent or solvent mixture is removed in vacuo and the mixture obtained is converted into a standard formulation after tie addition of standard fillers and auxiliaries.
Claim 19
Dependent Claim
51 words
S. A process for producing the fungicidal compositions claimed in one or more of Claims 1 to 5, characterised in that the fungicide(s) is/are dissolved or suspended in an organic solvent together with one or more phospholipides and optionally together with standard fillers and auxiliaries, after which the solvent is removed.
Claim 20
Dependent Claim
61 words
A process for producing the fungicidal compositions claimed in one or more of Claims 1 to 5, characterised in that one or more water-soluble or alcohol-soluble fungicides is/are dissolved in water or water/alcohol mixtures together with one or more phospholipides by stirring and/or gentle heating and/or by the application of ultrasonic waves, after which the solvent or solvent mixture is removed.
References Cited (Backward Citations)
US4007258A
Cited
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