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Pure Cefolac Powder For Oral Suspension Cefotaxime Cephalosporin CAS 79350 37 1

Basic Information
Place of Origin: China
Brand Name: Sengmei
Certification: ISO
Model Number: cefixime
Minimum Order Quantity: 1kg
Price: USD180~240/kg
Packaging Details: 1kg/bag;25kg/Durm
Delivery Time: 1-3work days
Payment Terms: T/T, Western Union, MoneyGram
Supply Ability: 5000kg per Month
Detail Information
Name: Cefixime CAS: 79350-37-1
EINECS: 616-684-4 Color: White Or White To Yellow Powder
Inventory Status: Enough Purity: 97%
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Product Description

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Cefixime Description
Cefixime is a third-generation oral cephalosporin antibiotic, also known as cefotaxime cephalosporin, vasomycin, and sulphon, clinically used for the treatment of Streptococcus (except Enterococcus), pneumonia chain Cocci, Neisseria gonorrhoeae, Escherichia coli, K. catarrhalis, Serratia, Citrobacter, Enterobacter cloacae, Enterobacter aerogenes, Haemophilus influenzae, Klebsiella, Serratia, morph Bacterial Infectious Diseases Caused by Bacillus and Influenza Bacteria.

Cefixime Function

The third generation of oral cephalosporins classes of broad spectrum antibiotics, gram-positive bacteria such as streptococcus, neisseria gonorrhoeae, influenza bacillus and other gram-negative bacteria, as well as to the crow, cephalosporin cefepime ammonia benzyl, cephalosporins hydroxylamine benzyl drug resistance of escherichia coli, klebsiella pneumoniae, singular proteus has strong antimicrobial effect, and the beta lactamase stability of various kinds of bacteria. Long-acting, highly effective and can be administered once a day. It is clinically used for respiratory tract infection, urethral infection and biliary tract infection caused by sensitive bacteria.

Cefixime Specification
PRODUCT NAME Cefixime
CAS no. 79350-37-1 Quantity 500kg
Storage In an airtight container, protected from light.
Items of analysis Specification Results
Description White or white to yellow powder Complies
Assay ≥95.0~102.0% 97.9%
Solubility Slightly soluble in water, soluble in methanol, sparingly soluble in anhydrous ethanol, practically insoluble in ethyl acetate Complies
Identification The retention times of the major peaks in the chromatogram of the assay preparation correspond to those of the Standard preparation obtained in the assay Complies
  The IR absorption spectrum of the substance to be examined corresponds to that of the reference standard Complies
PH 2.6~4.1 3.3%
Any impurity ≤0.5% 0.22%
Total impurity ≤3.0% 0.15%
Disregard limit ≤0.1% 0.02%
Ethanol ≤1.0% 0.66%
Water 9.0~12.0% 8.9%
Sulfated ash ≤0.2% 0.11%
Conclusion Conforms with enterprise standards

 

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