Molecular structure of Oxacillin Sodium Monohydrate, CAS Number: 7240-38-2
Oxacillin Sodium Monohydrate (CAS 7240-38-2)
Alternate Names:
Penicillin P-12; Bactocill; Cryptocillin
Application:
Oxacillin Sodium Monohydrate is a member of the penicillin class of antibiotics
CAS Number:
7240-38-2
Purity:
≥98%
Molecular Weight:
441.44
Molecular Formula:
C19H18N3NaO5S•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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SDS & Certificate of Analysis
Oxacillin Sodium Monohydrate is a derivative of penicillin. Oxacillin Sodium Monohydrate inhibits the synthesis of bacterial cell walls, making it effective against a wide range of gram-positive bacteria. Oxacillin Sodium Monohydrate is utilized in microbiology and biochemistry to study the mechanisms of antibiotic resistance and bacterial cell wall synthesis. Oxacillin Sodium Monohydrate is used as a selective agent in culture media to isolate and identify Staphylococcus species. Its stability and solubility properties make it in the study of bacterial physiology and antibiotic resistance mechanisms.
Oxacillin Sodium Monohydrate (CAS 7240-38-2) References
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- Simultaneous determination of five beta-lactam antibiotics in bovine milk using liquid chromatography coupled with electrospray ionization tandem mass spectrometry. | Riediker, S. and Stadler, RH. 2001. Anal Chem. 73: 1614-21. PMID: 11321318
- Analysis of beta-lactam antibiotics in incurred raw milk by rapid test methods and liquid chromatography coupled with electrospray ionization tandem mass spectrometry. | Riediker, S., et al. 2001. J Agric Food Chem. 49: 4171-6. PMID: 11559105
- Methicillin-resistant Staphylococcus aureus: comparison of susceptibility testing methods and analysis of mecA-positive susceptible strains. | Sakoulas, G., et al. 2001. J Clin Microbiol. 39: 3946-51. PMID: 11682512
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- Analysis of 12 beta-lactam antibiotics in human plasma by HPLC with ultraviolet detection. | McWhinney, BC., et al. 2010. J Chromatogr B Analyt Technol Biomed Life Sci. 878: 2039-43. PMID: 20561826
- QSRR analysis of β-lactam antibiotics on a penicillin G targeted MIP stationary phase. | Kempe, H. and Kempe, M. 2010. Anal Bioanal Chem. 398: 3087-96. PMID: 20936264
- The mixture toxicity of environmental contaminants containing sulfonamides and other antibiotics in Escherichia coli: Differences in both the special target proteins of individual chemicals and their effective combined concentration. | Long, X., et al. 2016. Chemosphere. 158: 193-203. PMID: 27269994
- Production of anti-amoxicillin ScFv antibody and simulation studying its molecular recognition mechanism for penicillins. | Liu, J., et al. 2016. J Environ Sci Health B. 51: 742-50. PMID: 27383141
- Virtual mutation and directional evolution of anti-amoxicillin ScFv antibody for immunoassay of penicillins in milk. | He, X., et al. 2017. Anal Biochem. 517: 9-17. PMID: 27780696
- High-Throughput Screening of Cell Transfection Enhancers Using Miniaturized Droplet Microarrays. | Liu, Y., et al. 2020. Adv Biosyst. 4: e1900257. PMID: 32293151
- Improving the chromatographic selectivity of β-lactam residue analysis in milk using phenyl-column chemistry prior to detection by tandem mass spectrometry. | Di Rocco, M., et al. 2020. Anal Bioanal Chem. 412: 4461-4475. PMID: 32447520
- Application of differential thermal analysis to compatibility and stability problems in penicillin-stearic acid mixtures. | Jacobson, H. and Reier, G. 1969. J Pharm Sci. 58: 631-3. PMID: 5796459
- Evaluation of mixed mode solid phase extraction cartridges for the preconcentration of beta-lactam antibiotics in wastewater using liquid chromatography with UV-DAD detection | E. Benito-Peña, A.I. Partal-Rodera, M.E. León-González, M.C. Moreno-Bondi. 2006. Analytica Chimica Acta. 556: 415-422.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Oxacillin Sodium Monohydrate, 1 g | sc-205781 | 1 g | $41.00 | |||
Oxacillin Sodium Monohydrate, 5 g | sc-205781A | 5 g | $143.00 |