23.
    发明专利
    未知

    公开(公告)号:DE10026139A1

    公开(公告)日:2001-11-29

    申请号:DE10026139

    申请日:2000-05-26

    Applicant: BASF AG

    Abstract: The invention relates to a method for the selective crystallization of poly- or monomethylol alkanoic acids of the general formula (I), wherein R is the same or different and represents a methylol group or a substituted or unsubstituted aliphatic hydrocarbon, with an essentially monomodal particle size distribution. This particle size distribution is achieved by crystallization in a temperature interval of from 85 DEG C to 50 DEG C observing a cooling rate of

    CRYSTALLINE MODIFCATIONS TO PYRACLOSTROBIN

    公开(公告)号:ZA200800504B

    公开(公告)日:2011-02-23

    申请号:ZA200800504

    申请日:2008-01-17

    Applicant: BASF AG

    Abstract: Crystalline modification IV of pyraclostrobin (A) exhibits at least three reflexes in an X-ray powder diffractogram at 25[deg]C, where the reflections (d) are 6.02 +- 0.01 Å, 4.78 +- 0.01 Å, 4.01 +- 0.01 Å, 3.55 +- 0.01 Å and 3.01 +- 0.01 Å. Independent claims are included for: (1) the preparation of (A); (2) crystalline modification II of pyroclostobin (A1) exhibiting at least four reflexes in a X-ray powder diffractogram at 25[deg]C, where the reflections (d) are 5.93 +- 0.01 Å, 5.82 +- 0.01 Å, 4.89 +- 0.01 Å, 4.78 +- 0.01 Å, 4.71 +- 0.01 Å, 3.97 +- 0.01 Å, 3.89 +- 0.01 Å, 3.77 +- 0.01 Å, 3.75 +- 0.01 Å, 3.57 +- 0.01 Å and 3.43 +- 0.01 Å; (3) the preparation of (A1); and (4) a plant protection agent, which comprises pyraclostrobin in the form of modification IV or in the form of modification II and carrier materials and/or additives. ACTIVITY : Fungicide. MECHANISM OF ACTION : None given.

    29.
    发明专利
    未知

    公开(公告)号:AT249426T

    公开(公告)日:2003-09-15

    申请号:AT99125660

    申请日:1999-12-22

    Applicant: BASF AG

    Abstract: Preparation of guanidine derivatives (I) comprises reacting O-alkylisourea salts (II) with an amine (III) in the presence of seed crystals of (I). Preparation of guanidine derivatives of formula (I) comprises reacting O-alkylisourea salts of formula (II) with an amine of formula (III) in the presence of seed crystals of (I). R1 = 1-8C alkylene or a divalent 5-10C cycloaliphatic group; R2 = H or 1-8C alkyl; or NR1R2 = 5-6 membered ring substituted by Z; Z = COOR3, SO2OR3 or PO(OR3)(OR4); R3 = H, alkalimetal or an equivalent of an alkaline earth metal; and R4 = as for R3 or 1-6C alkyl; R5 = 1-8C alkyl; X = equivalent of an anion.

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