Polymorphism and crystallization of p-aminobenzoic acid

被引:122
作者
Gracin, S [1 ]
Rasmuson, ÅC [1 ]
机构
[1] Royal Inst Technol, Dept Chem Engn & Technol, SE-10044 Stockholm, Sweden
关键词
D O I
10.1021/cg049954h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
p-Aminobenzoic acid (PABA) crystallizes in two different polymorphic forms: the alpha-polymorph, which is the commercially available form and appears as long, fibrous needles, and the beta-polymorph, which appears in the form of prisms. The thermodynamic stability and crystallization from different solvents have been studied experimentally. The system is found to be enantiotropic with a transition temperature of 25degreesC, below which the beta-form is the stable polymorph. The compound has been crystallized from 13 different solvents, either by slow cooling after which the product is allowed to mature in suspension, or by rapid cooling followed by immediate isolation. Needles were obtained from all solvents by both methods. In water and in ethyl acetate, at slow cooling below 20degreesC, the prismatic beta-form is obtained, however, often together with the needles. The beta-form crystals usually needed hours or days to grow at the very slow cooling used, while needles usually appeared in seconds. By careful control of supersaturation and temperature, cooling crystallization can be performed to produce the pure beta-form in water and in ethyl acetate. The influence of the solvent is explained by analysis of the crystal structures versus the possible interaction of the solvent molecules with the solute in solution. The alpha-form structure is governed by carboxylic acid dimers and is kinetically favored since it is believed that the corresponding dimers easily form in the solution, especially in less polar solvents.
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页码:1013 / 1023
页数:11
相关论文
共 31 条
[1]  
ALLEAUME M, 1966, CR ACAD SCI C CHIM, V262, P416
[2]   NMR-STUDY OF SOLID P-AMINO BENZOIC-ACID - STRUCTURE AND GROUP ROTATION [J].
BANERJEE, AK ;
AGRAWAL, P ;
GUPTA, RC .
JOURNAL FUR PRAKTISCHE CHEMIE, 1973, 315 (02) :251-257
[3]  
Bernstein J, 1999, ANGEW CHEM INT EDIT, V38, P3440, DOI 10.1002/(SICI)1521-3773(19991203)38:23<3440::AID-ANIE3440>3.0.CO
[4]  
2-#
[5]   PATTERNS IN HYDROGEN BONDING - FUNCTIONALITY AND GRAPH SET ANALYSIS IN CRYSTALS [J].
BERNSTEIN, J ;
DAVIS, RE ;
SHIMONI, L ;
CHANG, NL .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1995, 34 (15) :1555-1573
[6]  
Bernstein J., 2020, Polymorphism in Molecular Crystals, Vsecond
[7]   Polymorph selection: Challenges for the future? [J].
Blagden, N ;
Davey, RJ .
CRYSTAL GROWTH & DESIGN, 2003, 3 (06) :873-885
[8]  
Brittain H. G., 1999, Polymorphism in Pharmaceutical Solids
[9]   POLYMORPHISM OF PHARMACEUTICALS AND OTHER MOLECULAR-CRYSTALS .1. THEORY OF THERMODYNAMIC RULES [J].
BURGER, A ;
RAMBERGER, R .
MIKROCHIMICA ACTA, 1979, 2 (3-4) :259-271
[10]  
Davey R. J., 1993, FARADAY DISCUSS, V95, P160