Ezetimibe BP-USP

Ezetimibe BP-USP Specification

Molecular Weight
409.43

Structural Formula
C24H21F2NO3.

Loss on Drying
6.0%

Melting Point
164-166 C

Storage
Dry Place

Shelf Life
3 Years

Boiling point
654.9 C at 760 mmHg

Solubility
Freely soluble in alcohol Insoluble in aqueous solvent

Medicine Name
Ezetimibe

Chemical Name
Ezetimibe intermediates.

CAS No
163222-33-1

Type
Pharmaceutical Intermediates

Grade
Industrial Grade

Usage
Pharmaceutical and Food grade

Purity(%)
98.0-102.0%

Appearance
White crystalline powder

Physical Form
Powder

Ezetimibe BP-USP Trade Information

Minimum Order Quantity
5 Kilograms

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

About Ezetimibe BP-USP

Ezetimibe is used alone or combination with diet and other cholesterol-lowering medicines (eg, fenofibrate, statins) to treat high cholesterol and triglyceride (fats) levels in the blood, in patients with heterozygous familial hypercholesterolemia (HeFH), homozygous familial hypercholesterolemia (HoFH), or homozygous familial sitosterolemia.

Product Features

Ezetimibe BP-USP is available in powder form and demonstrates a high purity level, ensuring reliable results for industrial and pharmaceutical applications. Its prominent physical characteristics include a white crystalline appearance and distinct solubility profile, making it ideal for precise formulation requirements.

Application and Benefits

Widely utilized as a pharmaceutical intermediate, Ezetimibe BP-USP serves as a core ingredient in drug manufacturing. Its purity and stability contribute to consistent product performance, and it is suitable for both pharmaceutical and approved food-grade uses. This compound guarantees compliance with global quality standards.

Storage and Handling

To preserve quality and extend shelf life, Ezetimibe BP-USP should be stored in a dry environment for up to three years. Proper handling and storage are key to preventing degradation and ensuring the material maintains its intended properties over time.

FAQs of Ezetimibe BP-USP:

Q: How should Ezetimibe BP-USP powder be stored to maintain quality?

A: Ezetimibe BP-USP should be stored in a dry place to prevent moisture absorption and ensure its chemical stability throughout its three-year shelf life.

Q: What is the primary usage of Ezetimibe BP-USP?

A: Ezetimibe BP-USP is mainly used as a pharmaceutical intermediate for the preparation of medications and is also suitable for certain food-grade applications.

Q: When does the shelf life of Ezetimibe BP-USP expire?

A: When stored properly in a dry environment, Ezetimibe BP-USP retains stability for up to three years from its manufacturing date.

Q: Where can Ezetimibe BP-USP be sourced from?

A: Ezetimibe BP-USP is available for export, manufacture, and supply by various companies in India specializing in pharmaceutical intermediates.

Q: What benefits does the high purity (98.0102.0%) of Ezetimibe BP-USP offer?

A: High purity ensures optimal effectiveness and consistency in pharmaceutical production, reducing risks of contamination and supporting regulatory compliance.

Q: How is Ezetimibe BP-USP typically processed in pharmaceutical manufacturing?

A: Ezetimibe BP-USP is incorporated as an intermediate in the synthesis of final active pharmaceutical ingredients, benefiting from its defined purity and solubility properties.

Tell us about your requirement