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Soluble polyvinylpyrrolidone Povidone

Modern acetylene chemistry is based on the work of Reppe. One of the many products of this work is N-vinylpyrrolidone (Fig. 1). [Pg.1]

The first polymerization product of N-vinylpyrrolidone was soluble polyvinylpyrrolidone, which was patented in 1939. Fig. 2 and 3 show mechanisms of polymerization free-radical polymerization in water using hydrogen peroxide as initiator or in 2-propanol using an organic peroxide as initiator [1,141]. [Pg.1]

The mechanism for terminating the polymerization reaction makes it possible to produce soluble polyvinylpyrrolidone of almost any molecular weight. [Pg.1]

Apart from the method of production in water shown in Fig. 2, it is also possible to conduct the polymerization in an organic solvent, e.g. 2-propanol, an with [Pg.1]

The low and medium-molecular weight grades of soluble polyvinylpyrrolidone are spray-dried to produce the pharmaceutical-grade povidone powders, while the high-molecular weight grades are roller-dried. [Pg.2]


Today, soluble polyvinylpyrrolidone (povidone) is one of the most versatile and widely used pharmaceutical auxiliaries (see Section 2.4). [Pg.3]

In systematic investigations into the dependence of complex formation on structure, no difference was found between soluble polyvinylpyrrolidone (povidone) and insoluble polyvinylpyrrolidone (crospovidone) for complexes with organic compounds [192]. [Pg.28]


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