CEFUROXIME SODIUM

PRODUCT IDENTIFICATION

CAS NO. 56238-63-2

CEFUROXIME SODIUM 

EINECS NO. 260-073-1
FORMULA C16H15N4O8SNa
MOL WT. 446.38

H.S. CODE

2941.90

TOXICITY

 

SYNONYMS Sodium cefuroxime; Zinacef;
(6R,7R)-3-carbamoyloxymethyl-7-[2-(2-furyl)-2-[(Z)-methoxyimino]acetamido]-8-oxo-5-thia-1- azabicyclo[4.2.0]oct-2-ene-2-carboxylate, monosodium; Sodium [6R-[6alpha,7beta (Z)]]-3-[[(aminocarbonyl)oxy]methyl]-7-[2-furyl(methoxy imino)acetamido]-8-oxo-5-thia-1 -azabicyclo[4.2.0]oct-2-ene-2-carboxylate; Natrium-[6R-[6alpha, 7beta (Z)]]-3-[[(aminocarbonyl) oxy] methyl]-7-[2-furyl(methoxy imino)acetamido]- 8-oxo-5-thia-1-azabicyclo[4.2.0]oct- 2-en-2-carboxylat; [6R-[6alpha,7á (Z)]]-3-[[(aminocarbonil)oxi] metil]-7-[2-furil(metoxi imino)acetamido]- 8-oxo-5-tia-1- azabiciclo[4.2.0] oct-2-eno-2-carboxilato de sodio; [6R-[6alpha,7beta (Z)]]-3-[[(aminocarbonyl) oxy]méthyl]-7-[2-furyl(méthoxy imino)acétamido]-8- oxo-5-thia-1-azabicyclo [4.2.0]oct-2-ène-2- carboxylate de sodium

CLASSIFICATION

ANTIBOITICS / CEPHALOSPORINS /

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE White to slightly yellowish powder
MELTING POINT  
BOILING POINT  
SPECIFIC GRAVITY  
SOLUBILITY IN WATER  
pH  
VAPOR DENSITY

 

AUTOIGNITION

 

NFPA RATINGS

 

REFRACTIVE INDEX

 
FLASH POINT

 

STABILITY Stable under ordinary conditions.

APPLICATIONS

Cephalosporin: any of a group of broad-spectrum derived from species of fungi of the genus Cephalosporium  and are related to the penicillins in both structure and mode of action but relatively penicillinase-resistant antibiotics. These antibiotics have low toxicity for the host, considering their broad antibacterial spectrum. They have the active nucleus of beta-lactam ring which results in a variety of antibacterial and pharmacologic characteristics when modified mainly by substitution at 3 and 7 positions. Their antibacterial activities result from the inhibition of mucopeptide synthesis in the cell wall. They are widely used to treat gonorrhea, meningitis, pneumococcal, staphylococcal and streptococcal infections. The cephalosporin class of antibiotics is usually divided into generations by their antimicrobial properties. Three generations of cephalosporins are recognized and the fourth has been grouped. Each newer generation of cephalosporins has broader range of activity against gram-negative organisms but a narrower range of activity against gram-positive organisms than the preceding generation. The newer agents have much longer half-lives resulting in the decrease of dosing frequency. Accordingly, the third-generation cephalosporins can penetrate into tissues well, and thus antibiotic levels are good in various body fluids. Second-generation cephalosporins have broader spectrums of activity against gram negative coverage but less active against gram-positive organisms than first-generation agents. This group includes cefamandole (CAS RN 34444-01-4), cefaclor (53994-73-3), cefuroxime (55268-75-2), cefonicid (61270-58-4), ceforanide (60925-61-3). Cefoxitin (35607-66-0) and cefotetan (69712-56-7) which are effectively active against bacteroides fragilis are also included in this group, although they are cephamycins actually.
SALES SPECIFICATION

APPEARANCE

White to slightly yellowish powder

ASSAY

855 - 1,002µg/mg
MOISTURE 3.5% max

pH

6.0 - 8.5

HEAVY METALS

20ppm max

TRANSPORTATION
PACKING

5kgs - 25kgs

HAZARD CLASS  
UN NO.  
OTHER INFORMATION

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