Content s
1. Description
2. Physical Properties
2.1 Infrared Spectrum
2.2 Nuclear Magnetic Resonance Spectrum
2.3 Ultraviolet Spectrum
2.4 Optical Rotation
2.5 Melting Range
2.6 Differential Thermal Analysis
2.7 Solubility
2.8 pKa
2.9 Crystal Properties
3. Synthesis
4. Stability
5. Drug Metabolic Products
6. Methods of Analysis
6.1 Elemental Analysis
6.2 Non-Aqueous Titration of Cefazolin
6.3
6.4 Thin-Layer Chromatography
6.5
6.6
6.7 Federal Register Methods
Non-Aqueous Titration of Cefazolin Sodium
Spectrophotometric – UV Hydroxylamine Method
High Pressure Liquid Chromatographic Procedure