Date published: 2026-2-7

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Cefprozil monohydrate (CAS 121123-17-9)

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Alternate Names:
Cefzil
CAS Number:
121123-17-9
Molecular Weight:
407.44
Molecular Formula:
C18H19N3O5S•H2O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Cefprozil monohydrate is a stabilized hydrate form of cefprozil, a broad-spectrum, second-generation cephalosporin antibiotic known for its efficacy in treating a variety of bacterial infections. This antibiotic works by targeting and inhibiting penicillin-binding proteins (PBPs), which are critical for the synthesis of bacterial cell walls. By binding to these proteins, cefprozil monohydrate disrupts the cell wall synthesis process, particularly the cross-linking of peptidoglycan chains, which compromises the structural integrity of the bacterial cell wall, leading to cell lysis and death. This mechanism makes it effective against a range of both Gram-positive and Gram-negative bacteria. In research settings, cefprozil monohydrate has been extensively studied to understand its pharmacological properties, including absorption, distribution, metabolism, and excretion (ADME), as well as its clinical efficacy and resistance patterns. These investigations help in optimizing dosing regimens and understanding the scope of bacterial resistance, thereby informing clinical strategies for its use in non-therapeutic investigative scenarios focused on bacterial pathogenesis and antibiotic action.


Cefprozil monohydrate (CAS 121123-17-9) References

  1. Different approaches in manipulating ratio spectra applied for the analysis of Cefprozil in presence of its alkaline-induced degradation product: a comparative study.  |  Attia, KAM., et al. 2015. Spectrochim Acta A Mol Biomol Spectrosc. 145: 289-294. PMID: 25791886
  2. Stability indicating methods for the analysis of cefprozil in the presence of its alkaline induced degradation product.  |  Attia, KA., et al. 2016. Spectrochim Acta A Mol Biomol Spectrosc. 159: 1-6. PMID: 26814624
  3. Aquasomes nanoformulation for controlled release of drug and improved effectiveness against bacterial infections.  |  Shanmugam, B. and Srinivasan, UM. 2024. Ther Deliv. 15: 95-107. PMID: 38174590
  4. Activity of amoxicillin-clavulanate against penicillin-resistant Streptococcus pneumoniae in an experimental respiratory infection model in rats.  |  Smith, GM., et al. 1998. Antimicrob Agents Chemother. 42: 813-7. PMID: 9559788
  5. Flavonol Glycosides from the Flowers of crinum bulbispermum[J].  |  ABOU A H, ABOUL-ELA A, HAMMODA H M., 2005,. Alex. J. Pharm. Sci. 19(2):: l1g.
  6. Development and evaluation of a ready to use paediatric antibiotic suspension[J]. Int. J. Adv. Pharm. Nanotech, 2011, 1(2): 71-77.  |  Kathpalia H, Shidhaye S, Mittal S. 2011,. Int. J. Adv. Pharm. Nanotech,. 1(2):: 71-77.
  7. Dissolution Study of Some Antibiotics[J].  |  Sharma P, Tiwary L K. 2012. Oriental Journal of Chemistry,., 28(4).: 1889.
  8. Identification, isolation, and characterization of unknown degradation products of Cefprozil monohydrate by high-performance thin-layer chromatography[J].  |  Gawande V, Bothara K. 2014,. JPC–Journal of Planar Chromatography–Modern TLC,. 27:: 372-376.
  9. Commercial synthesis of cefprozil: development and control of process impurity[J].  |  Prakash Rai B, Tewari N, Nizar H. 2014. Organic Process Research & Development,., 18(5):: 662-664.
  10. Determination and correlation of solubility of cephradine and cefprozil monohydrate in water as a function of pH[J].  |  Sun H, Jiang C, Liu B,. 2017,. Journal of Chemical & Engineering Data,. 62(10):: 3423-3430.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Cefprozil monohydrate, 1 g

sc-285282
1 g
$62.00

Cefprozil monohydrate, 5 g

sc-285282A
5 g
$267.00