Molecular Formula | C22H22N6O5S2 |
Molar Mass | 514.58 |
Storage Condition | 2-8°C(protect from light) |
Physical and Chemical Properties | White to yellowish white crystalline powder, slightly specific odor. More soluble in water, a few do not dissolve in ethanol or ether. When the pH value is 5~7, it is soluble in water, and its aqueous solution stability can be compared with that of cefotaxime and other third generation cephalosporins. Acute toxicity LD50 mice, rats (g/kg):1.9~2.4,1.9~2.15 intravenous injection; 3.8~4.2,5.8~6.55 intraperitoneal injection. Cefpirome Sulfate: 022H22N6O5S2? H2SO4. [98753-19-6]. Crystallization, melting point 198~202 C (decomposition). [Α] D23-4.7 °(C = 5, water). UV maximum absorption: 265MN (φ21100). Solubility was> 6.5 in buffer at Ph = 50%. |
Hazard Symbols | Xi - Irritant |
Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. R42/43 - May cause sensitization by inhalation and skin contact. |
Safety Description | S22 - Do not breathe dust. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. |
Toxicity | LD50 in mice, rats (g/kg): 1.9-2.4, 1.9-2.15 i.v.; 3.8-4.2, 5.8-6.55 i.p. (Donaubauer, Mayer) |
white to yellowish crystalline powder with slight specific odor. Soluble in water, almost insoluble in ethanol or ether.
cefotaxime and 2,3 cyclopentenopyridine in the presence of potassium iodide, heated in water, cefpirome. Alternatively, cefpirome is also obtained by converting its side chain to iodide and refluxing 2, 3-cyclopentenopyridine in dichloromethane. Cefpirome was further salified with sulfuric acid to obtain cefpirome sulfate.
cefpirome sulfate is a new type of cephalosporin antibiotics, the drug was successfully developed by the German Hoechst, and in 1992 first in Mexico, Sweden market, trade name Cefrom. Broad antibacterial spectrum, strong antibacterial activity, the antibacterial effect of Staphylococcus aureus and cefotiam the same I Pseudomonas aeruginosa and piperacillin, gentamicin similar. It is stable against β-lactamases, including various plastid-mediated penicillinase and chromosome-mediated cephalosporinase. For sepsis and severe urinary tract infection, respiratory tract infection.