Cefuroxime Axetil -BP-USP-EP

Cefuroxime Axetil -BP-USP-EP Specification

Molecular Weight
510.474

Solubility
Freely soluble in acetone.

Heavy Metal (%)
20 ppm

Molecular Formula
C20H22N4O10S

Loss on Drying
1.3%

Storage
Dry Place

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

About Cefuroxime Axetil -BP-USP-EP

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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