Metronidazole BP-USP-EP

Metronidazole BP-USP-EP Specification

Molecular Weight
171.156 g/mol

Molecular Formula
C6H9N3O3

Storage
Dry Place

Shelf Life
5 Years

Solubility
Practically insoluble in water,freely soluble in methylene chloride, soluble in acetone ,slightly soluble in alcohol.

Particle Size
0.5%

Medicine Name
Metronidazole

Chemical Name
Flagyl; Metronidazol; Anagiardil; Trichazol

CAS No
443-48-1

Type
Pharmaceutical Intermediates

Grade
Medicine Grade

Usage
Pharmaceutical

Purity(%)
Not less than 98.5%-101.0%

Appearance
White or slightly yellowish crystalline powder or flakes

Physical Form
Powder

Metronidazole BP-USP-EP Trade Information

Minimum Order Quantity
500 Kilograms

Main Export Market(s)
Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa

About Metronidazole BP-USP-EP

Metronidazole belongs to the class of medicinesknown as antibiotics. It works by killing bacteria or preventing their growth.However, this medicine will not work for colds, flu, or other virus infections.This medicine is available only with your doctors prescription.

Versatile Antimicrobial Applications

Metronidazole is widely recognized for its effectiveness in combating anaerobic bacteria and protozoal infections. Its reliable quality and purity make it an essential active pharmaceutical ingredient for various medicinal formulations, offering robust antimicrobial properties for a broad spectrum of clinical needs.

Superior Pharmaceutical Grade Quality

This medicine-grade powder is meticulously manufactured to meet BP, USP, and EP standards, ensuring not less than 98.5%-101.0% purity. The consistent particle size and stable crystalline form enhance formulation performance, stability, and efficacy in pharmaceutical products.

Long-term Stability and Proper Storage

Metronidazole should be stored in a dry place to maintain its efficacy and physical appearance for up to 5 years. The products stability and shelf life support global distribution and bulk supply without compromising product integrity.

FAQs of Metronidazole BP-USP-EP:

Q: How is Metronidazole BP-USP-EP typically used in pharmaceuticals?

A: Metronidazole BP-USP-EP is primarily used as an active ingredient in the formulation of medicines to treat bacterial and protozoal infections. It serves as a key pharmaceutical intermediate in tablets, capsules, and topical preparations.

Q: What benefits does its high purity (98.5%-101.0%) provide?

A: A high purity range ensures consistent therapeutic performance, minimizes impurities, and enhances the safety profile of final pharmaceutical products, making the compound suitable for strict pharmaceutical standards and regulatory requirements.

Q: When should Metronidazole be stored and what is its shelf life?

A: Metronidazole should be stored in a dry place away from direct light and moisture. When properly stored, it exhibits a shelf life of up to 5 years, ensuring long-term availability for pharmaceutical manufacturing.

Q: Where is Metronidazole BP-USP-EP produced and supplied?

A: This compound is exported, manufactured, and supplied from India by reputable pharmaceutical intermediates companies, ensuring reliable global distribution to meet market demands.

Q: What is the physical appearance and solubility profile of Metronidazole powder?

A: Metronidazole appears as a white or slightly yellowish crystalline powder or flakes. It is practically insoluble in water, freely soluble in methylene chloride, soluble in acetone, and slightly soluble in alcohol, impacting its formulation choices.

Q: How is Metronidazole processed for pharmaceutical formulations?

A: Metronidazole powder is processed via precise weighing, particle size adjustment, blending, and formulation with excipients. Its high-grade quality supports seamless integration into different dosage forms while maintaining stability and activity.

Q: What is the main advantage of using Metronidazole BP-USP-EP as a pharmaceutical intermediate?

A: The key advantage lies in its proven efficacy against various microbial organisms, coupled with regulated quality standards (BP, USP, EP), ensuring safety and reliability in finished medicinal products.

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