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CAS RN: 7240-38-2 | Product Number: O0353
Oxacillin Sodium Salt Monohydrate
×
Purity: >95.0%(T)
Synonyms:
Product Documents:
| Size | Unit Price | Belgium | Japan* | Quantity |
Shipping Information
|
|---|---|---|---|---|---|
| 1G |
20,00 €
|
2 | 6 |
|
|
| 5G |
65,00 €
|
Contact Us | 2 |
|
|
| 25G |
207,00 €
|
Ships within 5 weeks after ordering | 6 |
|
* Stock available in Belgium: Shipment on the same day
* Stock available in Japan: Please check the Shipping Simulation for estimated shipments. (excludes regulated items and dry ice shipments)
Supplemental Product Information:
This product has not been tested for potency and is guaranteed for chemical purity.
| Product Number | O0353 |
Purity / Analysis Method 
|
>95.0%(T) |
| Molecular Formula / Molecular Weight | C__1__9H__1__8N__3NaO__5S·H__2O = 441.44 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature
|
Refrigerated (0-10°C) |
| Store Under Inert Gas | Store under inert gas |
| Condition to Avoid | Hygroscopic,Heat Sensitive |
| Packaging and Container
|
1G-Glass Bottle with Plastic Insert (View image) |
| CAS RN | 7240-38-2 |
| Related CAS RN
|
66-79-5&1173-88-2 |
| Reaxys Registry Number | 4287093 |
| PubChem Substance ID | 87560310 |
| Merck Index (14) | 6904 |
| MDL Number | MFCD00167146 |
Specifications
| Appearance | White to Almost white powder to crystal |
| Purity(HPLC) | min. 98.0 area% |
| Purity(Volumetric Analysis) | min. 95.0 % |
| Specific rotation [a]20/D | +200.0 to +215.0 deg(C=1, H2O)(calcd.on anh.substance) |
| Water | 3.5 to 5.0 % |
| NMR | confirm to structure |
Properties (reference)
| Melting Point | 188 °C(dec.) |
| Specific Rotation | 205° (C=1,H2O) |
GHS
Related Laws:
Transport Information:
| HS Number | 2941100000 |
Application
Oxacillin Sodium: A β-Lactamase-Resistant Penicillin
Oxacillin sodium, an isoxazolyl penicillin, is chemically synthesized from 6-APA [A0800] and [M2996]. Oxacillin has activity against Gram-positive bacteria, but less activity against Gram-negative bacteria, the same as penicillin G [P1770] [P1772]. It acts as a competitive inhibitor of the enzyme transpeptidase, which is needed by bacteria to make their cell walls. Meanwhile, oxacillin, cloxacillin [C2244] and methicillin are resistant to the enzymes (β-lactamases) which produced by bacteria that destroy β-lactam antibiotics like penicillins and cephalosporins, due to theirs large side-chain, which does not allow the β-lactamases to bind. However, with the widespread use of oxacillin, antibiotic-resistant strains called oxacillin-resistant Staphylococcus aureus (ORSA) have become increasingly prevalent worldwide.
References
- A survey of the kinetic parameters of class C β-lactamases. Penicillins
- Contributions of the AmpC β-lactamase and the acrAB multidrug efflux system in intrinsic resistance of Escherichia coli K-12 to β-lactams
- Methicillin (oxacillin)-resistant Staphylococcus aureus strains isolated from major food animals and their potential transmission to humans
- Detection of methicillin/oxacillin resistance in staphylococci
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