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公开(公告)号:DE10137017A1
公开(公告)日:2003-02-20
申请号:DE10137017
申请日:2001-07-30
Applicant: BASF AG
Inventor: RAULS MATTHIAS , GELDER RICHARD VAN , WAGNER KATRIN , BERNARD HARALD
IPC: B01D9/02 , B01D9/00 , C07C403/00 , C07C403/08 , C07C403/14 , C07C403/20 , B01J19/10
Abstract: Production of crystals with an average particle size below 100 micro m comprises crystallizing a compound from a solution or suspension while exposing it to ultrasound directly applied through a sonotrode and while maintaining a specific stirring power.
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公开(公告)号:DE59805697D1
公开(公告)日:2002-10-31
申请号:DE59805697
申请日:1998-02-09
Applicant: BASF AG
Inventor: RAULS MATTHIAS , BAUMANN DIETER , WISTUBA HERMANN , OTTO BERNHARD
Abstract: Dicarboxylic acid crystals are prepared from a solution containing at least one organic dicarboxylic acid in a process in which at least one anionic polyelectrolyte having a molecular weight of at least 2000 is added to the solution before or during the crystallization.
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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
Inventor: SCHULZ GERHARD , WEIGL HAGEN , GELDER RICHARD VAN , RAULS MATTHIAS , EBEL KLAUS
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
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公开(公告)号:CA2218921A1
公开(公告)日:1998-05-29
申请号:CA2218921
申请日:1997-11-12
Applicant: BASF AG
Inventor: POTTHOFF-KARL BIRGIT , BAUMANN DIETER , LETZELTER THOMAS , ASCHERL HERMANN , SCH NHERR MICHAEL , RAULS MATTHIAS
IPC: C11D1/04 , C07C227/42 , C07C229/16 , C07C229/24 , C07C229/04 , C11D1/10 , C07D211/34 , C07C303/42 , C07D307/54 , C07D213/55 , C07C309/61
Abstract: A crystalline solid which has a sufficiently low hygroscopicity for processing and use and essentially consists of glycine-N,N-diacetic acid derivatives is prepared by adjusting the water content of the starting material containing the glycine-N,N-diacetic acid derivatives to a value of from 10 to 30% by weight, based on the starting material, and subsequently bringing about crystallization. .
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公开(公告)号:NO973866A
公开(公告)日:1998-02-24
申请号:NO973866
申请日:1997-08-22
Applicant: BASF AG
Inventor: GRIMMER KARL , PURUCKER BERNHARD , DITTMAR HEINRICH , RAULS MATTHIAS , MECKL STEFAN
CPC classification number: B01D53/1493
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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
Inventor: WUCKELT JORG , GOTZ RONALD , RAULS MATTHIAS , NOACK REINER , ERK PETER , COX GERHARD , MAYER WINFRIED , KROHL THOMAS , SCHNEIDER KARL-HEINRICH , VOGELBACHER UWE JOSEF , ZIEGLER HANS
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.
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公开(公告)号:UA89830C2
公开(公告)日:2010-03-10
申请号:UAA200800568
申请日:2006-06-19
Applicant: BASF AG
Inventor: ZIEGLER HANS , MAYER WINFRIED , KROEHL THOMAS , SCHNEIDER KARL-HEINRICH , COX GERHARD , ERK PETER , VOGELBACHER UWE JOSEF , NOACK RAINER , GOETZ ROLAND , WUCKELT JOERG , RAULS MATTHIAS
IPC: A01N47/24 , C07D231/22
Abstract: Данноеизобретениеотноситсяк новымкристаллическиммодификациямпираклостробина, кспособуихполученияи кприменениюновыхмодификацийдляполучениясредствдлязащитырастений.
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公开(公告)号:CA2612075A1
公开(公告)日:2006-12-28
申请号:CA2612075
申请日:2006-06-19
Applicant: BASF AG
Inventor: GOETZ ROLAND , KROEHL THOMAS , SCHNEIDER KARL-HEINRICH , COX GERHARD , ERK PETER , VOGELBACHER UWE JOSEF , NOACK RAINER , RAULS MATTHIAS , WUCKELT JOERG , ZIEGLER HANS , MAYER WINFRIED
IPC: A01N47/24 , C07D231/22
Abstract: The invention relates to novel crystalline modifications to pyraclostrobin, methods for production and use of the novel modifications for the production of plant protection agents.
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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
Inventor: KESSEL KNUT , KLUGE MICHAEL , GREINDL THOMAS , BOGENSTAETTER THOMAS , SCHERR GUENTER , RAULS MATTHIAS , VAN GELDER RICHARD
IPC: C07C277/08 , C07C279/14 , C07C303/22 , C07C309/15 , C07F9/38
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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公开(公告)号:DE19962455A1
公开(公告)日:2001-06-28
申请号:DE19962455
申请日:1999-12-22
Applicant: BASF AG
Inventor: RIECHERS HARTMUT , HOEHN ARTHUR , SIMON JOACHIM , LANG ORTMUND , SCHOENMAKERS HARTMUT , RAULS MATTHIAS , CLAERBOUT KOEN
IPC: C07D487/08
Abstract: Preparation of a solution of pure triethylenediamine (TEDA) comprises vaporizing TEDA and passing the TEDA vapor into a liquid solvent. An Independent claim is also included for the preparation of pure TEDA by preparing the solution as above and crystallizing TEDA from this solution.
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