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Ranitidine molecular structure

When the FTIR spectra of polymorph systems differ substantially, the results may readily permit the identification of a particular form. For instance, the two forms of ranitidine hydrochloride yielded spectra that differed in the region above 3000 cm and in the regions spanning 2300-2700 cm and 1570-1620 cm b Zanoterone has been found to crystallize in a number of different forms, each of which yields a characteristic infrared spectrum. When solvent molecules are incorporated in a crystal lattice, the new structure is often sufficiently different from that of the anhydrous phase so that many of the molecular vibrational modes are altered. [Pg.2942]


See other pages where Ranitidine molecular structure is mentioned: [Pg.83]    [Pg.156]    [Pg.505]    [Pg.159]    [Pg.281]    [Pg.270]    [Pg.39]    [Pg.489]    [Pg.2304]    [Pg.106]   
See also in sourсe #XX -- [ Pg.14 , Pg.14 , Pg.285 , Pg.371 ]




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Ranitidine

Ranitidine, structure

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