The polymorphic forms II and III of paracetamol were obtained by melting the marketed form I. Under the melting and cooling conditions used, it was possible to obtain forms I, II and III. The recrystallization conditions and the physical properties of forms II and III were investigated by means of various techniques: thermomicroscopy, DSC analysis, infrared microspectrometry and X-ray powder diffraction at room temperature and as a function of temperature. Form III was found to be very unstable. However, its formation seems to be an important intermediate step in the preparation of form II.

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Mit Hilfe von DTA‐ und HT‐Röntgenanalysen werden im SrO‐reichen Teil des Systems die Verbindungen Srßi, O4, Sr3Bi2O6 und Sr2Bi2O5 (Pcmm, Z=4) charakterisiert.

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