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Cefuroxime Axetil -BP-USP-EP
Cefuroxime Axetil -BP-USP-EP

Cefuroxime Axetil -BP-USP-EP

Price 9500 INR/ Kilograms

MOQ : 25 Kilograms

Cefuroxime Axetil -BP-USP-EP Specification

  • Solubility
  • Freely soluble in acetone.
  • Molecular Formula
  • C20H22N4O10S
  • Storage
  • Dry Place
  • Heavy Metal (%)
  • 20 ppm
  • Loss on Drying
  • 1.3%
  • Molecular Weight
  • 510.474
  • Medicine Name
  • Cefuroxime axetil
  • Chemical Name
  • Ceftin; Zinnat; Elobact; Zinat; Cefuroxime 1-acetoxyethyl ester
  • CAS No
  • 64544-07-6
  • Type
  • Pharmaceutical Intermediates
  • Grade
  • Industrial Grade
  • Usage
  • Pharmaceutical
  • Purity(%)
  • 745 875 ug/mg
  • Appearance
  • A White or almost white powder
  • Physical Form
  • Powder
 

Cefuroxime Axetil -BP-USP-EP Trade Information

  • Minimum Order Quantity
  • 25 Kilograms
  • Main Export Market(s)
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
 

Cefuroxime Axetil -BP-USP-EP About

It is used to treat bacterialinfections in many different parts of the body. It belongs to the class ofmedicines known as cephalosporin antibiotics. It works by killing bacteria orpreventing their growth. However, this medicine will not work for colds, flu,or other virus infections.



Versatility and Application

Cefuroxime Axetil is utilized in the pharmaceutical industry as a crucial intermediate for crafting second-generation cephalosporin antibiotics. Its potent antibacterial properties make it a preferred choice for manufacturers developing drugs to combat a broad spectrum of infections. Its established efficacy ensures widespread use in both clinical and research settings.


Quality and Compliance Standards

Manufactured according to BP, USP, and EP standards, Cefuroxime Axetil ensures top-tier quality and regulatory compliance. Rigorous control over loss on drying (1.3%) and heavy metal content (20 ppm) guarantees safety and purity, making it a globally trusted choice for large-scale pharmaceutical production.

FAQs of Cefuroxime Axetil -BP-USP-EP:


Q: How is Cefuroxime Axetil primarily used in the pharmaceutical industry?

A: Cefuroxime Axetil serves as a key intermediate in producing cephalosporin antibiotics, notably for oral medications such as Ceftin and Zinnat, used to treat various bacterial infections.

Q: What are the benefits of using Cefuroxime Axetil in drug formulations?

A: With high purity, reliable solubility in acetone, and compliance with pharmaceutical standards, Cefuroxime Axetil enables consistent, effective antibiotic formulation and meets stringent safety requirements.

Q: When should Cefuroxime Axetil be stored, and under what conditions?

A: Cefuroxime Axetil must be stored in a dry place at ambient temperature to preserve its potency and prevent degradation from moisture or contaminants.

Q: Where is Cefuroxime Axetil manufactured and exported from?

A: It is predominantly produced, supplied, and exported from India by reputable pharmaceutical manufacturers adhering to international quality standards.

Q: What is the typical appearance and composition of Cefuroxime Axetil?

A: The compound appears as a white or almost white powder, with a molecular formula of C20H22N4O10S and a molecular weight of 510.474, signifying its distinct chemical profile.

Q: How is purity and safety ensured during the manufacturing process?

A: Comprehensive quality control processes limit loss on drying to 1.3% or less and heavy metal content to no more than 20 ppm, ensuring that the product meets both regulatory and safety benchmarks.

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