Product Details
Place of Origin: China
Brand Name: Sunshine
Certification: ISO,COA
Model Number: 35607-66-0
Payment & Shipping Terms
Minimum Order Quantity: Negotiation
Price: Negotiation
Packaging Details: Bag,Drum
Delivery Time: 7-15 days
Payment Terms: L/C, D/A, T/T, Western Union
Supply Ability: TON
CAS NO:: |
35607-66-0 |
Appearance:: |
White To Off-white Crystalline Powder |
Molecular Formula:: |
C16H17N3O7S2 |
Molecular Weight:: |
427.45200 |
EINECS NO:: |
252-641-2 |
MDL NO:: |
MFCD00072014 |
CAS NO:: |
35607-66-0 |
Appearance:: |
White To Off-white Crystalline Powder |
Molecular Formula:: |
C16H17N3O7S2 |
Molecular Weight:: |
427.45200 |
EINECS NO:: |
252-641-2 |
MDL NO:: |
MFCD00072014 |
Product Description:
Product Name: Cefoxitin CAS NO: 35607-66-0
Synonyms:
(6r-cis)-ethyl)-7-metho-xy-8-oxo-7-((2-thienylacetyl)amino);
Cefoxitin{(6R-cis)-3-[(Carbamoyloxy)methyl]-7-metho-xy-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid};
Chemical & Physical Properties:
Appearance: White to off-white crystalline powder
Assay :≥99.0%
Density: 1.63 g/cm3
Boiling Point: 843.4℃ at 760 mmHg
Melting Point: 149 – 150℃
Refractive Index: 1.692
Water Solubility: Predicted solubility in water is less than 0.2mg/ml
Safety Information:
HS Code: 3003201300
Packing Group: III
RIDADR: UN 3077
Cefoxitin is a semi-synthetic antibiotic derived from Cephamycin C, possessing high resistance to β-lactamase inactivation. An antibacterial. Cefoxitin contains the same C-7 side chain as cephalothin and the same C-3 side chain as cefuroxime. The most novel chemical feature of cefoxitin is the possession of an α-oriented metho-xyl group in place of the normal H-atom at C-7. This increased steric bulk conveys very significant stability against β-lactamases. The inspiration for these functional groups was provided by the discovery of the naturally occurring antibiotic cephamycin C derived from fermentation of Streptomyces lactamdurans. Cephamycin C itself has not seen clinical use but, rather, has provided the structural clue that led to useful agents such as cefoxitin. Agents that contain this 7α metho-xy group are commonly referred to as cephamycins. Ingenious chemical transformations now enable synthetic introduction of such a metho-xy group into cephalosporins lacking this feature.
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