Product name | Sulbactam |
Synonyms | (2S,5R)-3,3-dimethyl-4,4,7-trioxo-4位鈦?thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid;Penicillanicacid1,1-dioxide:CP-45899:CPL45899-2:Betamaze;4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid,3,3-dimethyl-7-oxo-,4,4-dioxide,(2S-cis)-;Betamaze;PenicillanicacidS,S-Chemicalbookdioxide;(2S,5R)-3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptan-2-carboxylicacid4,4-dioxid;(2S,5β)-2β-Carboxy-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane4,4-dioxide;(2S,5β)-3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2β-carboxylicacid4,4-dioxide |
CAS | 68373-14-8 |
Assay | 99% |
Appearance | White powder |
Melting point | 154-157℃ |
Boiling point | 567.7±50.0 °C(Predicted) |
β-lactamase inhibitor has strong irreversible inhibitory effect on penicillinase and cephalosporinase, and it is combined with cefoperazone to form a combined preparation of Sulperzon (Sulperzon) for the treatment of drug-resistant bacterial infections; and ampicillin Penicillin is formulated into a compound preparation compound ampicillin for the synthesis of sulbactam sodium
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