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Ketones ketoprofene

Ketalgin Ketoprofen Ketalgin Methadone HCI Ketaman Propantheline bromide Ketanest - Ketamine HCI Ketawrift - Allopurinol Ketazol Ketoconazole Ketazon - Kebuzone Ketazone Kebuzone Keteocort Prednisone Keteocort H Prednisolone Kethamed Pemoline Keto Ketoprofen Ketobun A Allopurinol Ketobutan Kebuzone Ketobutane Kebuzone Ketobutazone Kebuzone Ketocef Cefuroxime Ketofen Kebuzone Ketofen Ketoprofen Keton Ketoprofen Ketonal - Ketoprofen Ketophezon Kebuzone Ketopron Ketoprofen Ketoprosil Ketoprofen Ketoscillium Fentonium bromide Ketoval - Ketoprofen Kevadon - Ketoprofen Key-Pred Prednisolone acetate Key-Pred S.P. Prednisolone phosphate sodium... [Pg.1711]

Ketoglutaifo add, 283,286 Ketones, 275,298 Ketoprofen, 286 Kieselguhr, 117 Kihara potential, 206 Kinetic resistances, 227 Kinetics of adsorption-desorption, 10, 127, 159... [Pg.168]

Ketoprofen can also be determined using another classic, ion-selective electrode [76] with very similar parameters in between those of the two electrodes described above. The active ingredient of the polymer membrane is a complex of ketoprofen and rhoda-mine 6G. The electrode shows a deviation of (58.0 1.0 mV decade Hn the concentration range of 1.0 x 10 to 1.0 x 10 S detection limit of 6.3 x 10" mol L short response time of 3-4 s and lifetime of approx. 4 months. By using this electrode, ketoptofen was determined with a standard deviation of s 0.21 and s 0.27 in the following preparations Fastum gel (Berlin-Chemie/Menarini) and Ketonal injections (Sandoz). [Pg.216]

We previously mentioned the importance of determining the appropriate solvent for acyl transfer reactions (esterification and transesterification). Nevertheless, it is difficult to select a universal solvent for the esterification of (R,S) 2-arylpropionic acids. In fact, hydrophobic solvents such as cyclohexane [98,102], isooctane [97], or the mixtures isooctane/ChC or isooctane/toluene [100] are recommended for the highly hydrophobic substrates naproxen and ibuprofen (see Tables 6 and 7). On the contrary, moderately hydrophilic acids such as ketoprofen (Table 5 [92]) or flurbiprofen (Table 8 [111]) are better esterified in sUghtly hydrophilic solvents such as cffisopropyl ether, methylwobutyl ketone, or 1,4-dioxane. Iherefore, we can conclude that depending on the hydrophobicity of the substrate we must select the organic solvent in order to obtain the best catalytic performance. [Pg.681]


See other pages where Ketones ketoprofene is mentioned: [Pg.1711]    [Pg.1711]    [Pg.175]    [Pg.78]    [Pg.1743]    [Pg.20]    [Pg.65]    [Pg.62]    [Pg.216]    [Pg.79]    [Pg.161]    [Pg.1295]    [Pg.348]   
See also in sourсe #XX -- [ Pg.218 , Pg.279 ]




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Keton - Ketoprofen

Keton - Ketoprofen

Ketonal - Ketoprofen

Ketonal - Ketoprofen

Ketoprofen

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