High Quality Antibiotic API Powder Cefotaxime Sodium CAS 64485-93-4

• Powder: Yes
• Customized: Customized
• Certification: GMP, HSE, ISO 9001, USP, BP
• Suitable for: Elderly, Children, Adult
• State: White Crystalline Powder
• Purity: >99%
• Model NO.: Cefotaxime Sodium
• CAS: 64485-93-4
• Mf: C16h17n5nao7s2
• MW: 478.4547
• pH: 4.5-6.5
• Type: Antibiotic and Antimicrobial Agents
• Einecs No.: 264-915-9
• Shelf Life: 24 Month
• Storage: Cool Dry Place
• Transport Package: 1kg/Bag, 25kg/Drum
• Specification: Cefotaxime Sodium
• Trademark: HNB
• Origin: China
• Production Capacity: 2000kg/Month

Product Description

Product Name:  Cefotaxime sodium

CAS NO: 64485-93-4 

Purity: 99%min

Appearance:  This product is white, almost white or yellowish white crystalline powder; odorless or slight special smell. It is free soluble in water, slightly soluble in ethanol.
 

Application: 

Treatment of infections of lower respiratory tract including pneumonia, urinary tract, skin and skin structures, bone and joints; treatment of bacteremia/septicemia, CNS infections, intra-abdominal infections including peritonitis, gynecological infections including pelvic inflammatory disease, endometritis and pelvic cellulitis caused by susceptible strains of specific microorganisms; perioperative prophylaxis.

It is not as effective against cefazolin as Gram-positive bacteria. Enterococci are resistant to this product. It is not effective against -resistant pneumococcus. It has strong bactericidal activity against Gram-negative bacteria. It is effective against E. coli, influenza, bacillus, and singularities. Proteus and Salmonella have stronger effects than cefoperazone, weak or resistant to Bacteroides fragilis, and Pseudomonas aeruginosa and Enterobacter cloacae are not sensitive to this product.


 

ITEMS	SPECIFICATION	RESULTS
Appearance	White to pale yellow Crystalline Powder	Passed
Identification	IR Spectrum HPLC RT Sodium	Passed Passed Passed
Clarity	Clear	Passed
Color of Solution	NMT 0.2(430mm,10% solution)	Passed
Specific optical rotation	+56°~+64°	+61°
PH	4.5~6.5	5.5
Loss on drying	≤3.0%	2.7%
Chromatographic purity Individual impurity Total impurity	≤1.0% ≤3.0%	≤0.6% ≤2.0%
Sterility	Sterile	Passed
Bacterial Endotoxins	NMT 0.20 USP EU/mg	Passed
Particulate matter	≥10um NMT 6000 ≥25 um NMT 600	Passed Passed
Assay(HPLC)	916-964μg/mg	940μg/mg
Storage Condition	Preserve in tight container.