Date published: 2026-2-5

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Flucloxacillin sodium (CAS 1847-24-1)

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Alternate Names:
Floxapen Sodium; Staphylex Sodium; (2S,5R,6R)-6-[[[3-(2-Chloro-6-fluorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Sodium
Application:
Flucloxacillin sodium is A new semisynthetic penicillin
CAS Number:
1847-24-1
Molecular Weight:
475.85
Molecular Formula:
C19H16ClFN3O5S•Na
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Flucloxacillin sodium, with the CAS number 1847-24-1, is a sodium salt form of flucloxacillin, a beta-lactam antibiotic that belongs to the penicillinase-resistant group of penicillins. This compound is known for its ability to resist degradation by staphylococcal penicillinase enzymes, which are commonly involved in antibiotic resistance. The principal mechanism of action of Flucloxacillin sodium involves the inhibition of bacterial cell wall synthesis. It achieves this by binding to penicillin-binding proteins (PBPs) located on the inner membrane of the bacterial cell wall. These PBPs are enzymes that play a critical role in the cross-linking process of the bacterial cell wall′s peptidoglycan layer, which is essential for maintaining cell wall integrity and shape. By inhibiting these proteins, Flucloxacillin sodium disrupts the final stages of the bacterial cell wall assembly, leading to weakened cell walls, ultimately causing bacterial lysis and cell death. In research, Flucloxacillin sodium has been extensively used to study the dynamics of bacterial cell wall synthesis, the mechanism of action of beta-lactam antibiotics, and the molecular basis of resistance to penicillinase-producing bacteria. These investigations are crucial for understanding bacterial cell physiology, the development of bacterial resistance, and exploring new strategies to counteract resistant bacterial strains.


Flucloxacillin sodium (CAS 1847-24-1) References

  1. Pyrocatechol violet in pharmaceutical analysis. Part I. A spectrophotometric method for the determination of some beta-lactam antibiotics in pure and in pharmaceutical dosage forms.  |  Amin, AS. 2001. Farmaco. 56: 211-8. PMID: 11409329
  2. Determination of certain drugs in binary mixtures formulations by second derivative ratio spectrophotometry and LC.  |  El-Gindy, A., et al. 2004. Farmaco. 59: 703-12. PMID: 15337436
  3. Polymorphism of flucloxacillin sodium.  |  Zhou, XY., et al. 2011. Pharmazie. 66: 933-5. PMID: 22312697
  4. Assessment of the stability of citrate-buffered flucloxacillin for injection when stored in two commercially available ambulatory elastomeric devices: INfusor LV (Baxter) and Accufuser (Woo Young Medical): a study compliant with the NHS Yellow Cover Document (YCD) requirements.  |  Allwood, MC., et al. 2020. Eur J Hosp Pharm. 27: 90-94. PMID: 32153771
  5. Taste-Masked Flucloxacillin Powder Part 1: Optimisation of Fabrication Process Using a Mixture Design Approach.  |  Yoo, O., et al. 2023. Pharmaceuticals (Basel). 16: PMID: 37631086
  6. Bioavailability and half-life of two preparations of flucloxacillin.  |  Paton, DM., et al. 1982. N Z Med J. 95: 766-8. PMID: 6959033
  7. Stability of flucloxacillin in elastomeric infusion devices.  |  Carroll and Julia A. 2005. Journal of Pharmacy Practice and Research. 35.2: 90-93.
  8. A sensitive validated spectrophotometric method for the determination of flucloxacillin sodium.  |  Gujral, et al. 2009. Journal of Chemistry. 6: S397-S405.
  9. Development and validation of a UV-spectrophotometric method for determination of flucloxacillin sodium in capsules.  |  AM Fiorentino, et al. 2012. Current Pharmaceutical Analysis. 8.1: 101-106.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Flucloxacillin sodium, 10 mg

sc-207689
10 mg
$62.00

Flucloxacillin sodium, 100 mg

sc-207689A
100 mg
$75.00