91.
    发明专利
    未知

    公开(公告)号:DK1489906T3

    公开(公告)日:2007-10-01

    申请号:DK03712051

    申请日:2003-03-19

    Applicant: BASF AG

    Abstract: A new fungicidal mixture contains synergistic amounts of (1) prothioconazole (I) and (2) at least one of 20 other specific fungicides, e.g. boscalid, carboxine, metrafenone, quinoxyfen, fenoxanil, carbendazim, metalaxyl, prochloraz or anthraquinone. A fungicidal mixture contains synergistic amounts of the following active components: (1) prothioconazole (I) or its salt or adduct; and (2) one or more of boscalid, carboxine, metrafenone, N-(alpha -cyclopropoxyimino)-(2,3-difluoro-6-trifluoromethyl-benzyl)-phenylacetamide, N-(alpha -cyclopropoxyimino)-2,3-difluoro-6-difluoromethyl-benzyl)-phenylacetamide, quinoxyfen, dithianon, thiram, mepiquat chloride, cyazofamid, fenoxanil, 6-fluoro-2-(1-(2-(isopropoxycarbonylamino)-isovaleramido)-ethyl)-benzothiazole, thiophanate methyl, carbendazim, metalaxyl, fludioxonil, thiabendazole, quintozen, prochloraz and/or anthraquinone. Independent claims are included for: (a) a harmful fungus control method involving application of the mixture of (1) and (2) to the fungi, their habitat or plants, seeds, soil, surfaces, materials or regions to be protected ((1) and (2) being applied simultaneously, separately or successvely); and (b) a fungicidal composition comprising the (1)/(2) mixture together with a solid or liquid carrier. ACTIVITY : Fungicide. In tests for protective action against Blumeria graminis f. sp. triciti (mildew) in wheat, prothioconazole (I) at 1 ppm alone or boscalid (II) at 4 ppm alone gave no (0%) control, whereas a combination of 1 ppm (I) and 4 ppm (II) gave 92% control. MECHANISM OF ACTION : None given in the source material.

    FUNGICIDE MIXTURES BASED ON PYRIDINE AMIDES AND FENARIMOL

    公开(公告)号:CA2313323C

    公开(公告)日:2007-09-04

    申请号:CA2313323

    申请日:1998-12-15

    Applicant: BASF AG

    Abstract: The invention relates to fungicide mixtures containing, as active components, a) an amide compound of formula (I) A-CO-NR1R2, wherein A represents an aryl group or an aromatic or non-aromatic, 5- or 6-structured heterocyclic compound having 1 to 3 heteroatoms selected from O, N, S; whereby the aryl group or the heterocycli c compound can optionally comprise 1, 2 or 3 substituents selected independently of one another from alkyl, halogen, CHF2, CF3, alkoxy l, haloalkoxyl, alkylthio, alkyl sulfinyl and alkyl sulfonyl; R1 represents a hydrogen atom; R2 represents a phenyl group or cycloalkyl group optionally containing 1, 2 or 3 substituents selected independently of one another from alkyl, alkenyl, alkynyl, alkoxyl, alkenyloxyl, alkynyloxyl, cycloalkyl, cycloalkenyl, cycolalkyloxyl, cycloalkenyloxyl, phenyl and halogen, whereby the aliphatic and cycloaliphat ic radicals can be partially or completely halogenated and/or the cycloaliphatic radicals can be substituted by 1 to 3 alkyl groups, where by the phenyl group can contain 1 to 5 halogen atoms and/or 1 to 3 substituents selected independently of one another from alkyl, haloalky l, alkoxyl, haloxyl, alkylthio and haloalkylthio, and whereby the amidic phenyl group is optionally condensed with a saturated 5-structured ri ng which is optionally substituted by one or more alkyl groups and/or can comprise a heteroatom selected from O and S, and b) (~)-(2- chlorphenyl)(4-chlorphenyl)(pyrimidine-5-yl)methanol (a). The active components are provided in a synergistically effective quantity.

    98.
    发明专利
    未知

    公开(公告)号:DE50307422D1

    公开(公告)日:2007-07-19

    申请号:DE50307422

    申请日:2003-03-04

    Applicant: BASF AG

    Abstract: Fungicidal mixture comprises prothioconazole (I) and at least one triazole compound (II) comprising epoxiconazole, metconazole, propiconazole, fluquinconazole, penconazole, difenconazole, hexaconazole, cyproconazole, flusilazole, tetraconazole, fenbuconazole, myclobutanil, simeconazole, ipconazole or triticonazole. ACTIVITY : Plant Antifungal. In a test, wheat seedlings were treated with a spray containing prothioconazole (0.06 ppm) and epoxiconazole (1 ppm) and, after 24 hours, dusted with spores of Erysiphe graminis. Efficacy after 7 days was 78%, compared with a calculated value (Colby formula) of 44%. MECHANISM OF ACTION : None given.

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