Mannitol BP/USP

Mannitol BP/USP Specification

Storage
Dry Place

Molecular Weight
182.172

Shelf Life
5 Years

Molecular Formula
C6H14O6

Boiling point
295C

Melting Point
167-170 C(lit.)

Solubility
Stable. Combustible. Incompatible with strong oxidizing agents. Water Solubility: soluble

Chemical Name
D-Mannitol, mannite, manna sugar

CAS No
69-65-8

Type
Pharmaceutical Intermediates

Grade
Industrial Grade

Usage
Pharmaceutical use

Purity(%)
97.0%102.0%

Appearance
White crystalline powder

Physical Form
Powder

Mannitol BP/USP Trade Information

Minimum Order Quantity
100 Kilograms

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

About Mannitol BP/USP

Salius pharma do supply and Exports of Mannitolis adiuretic medication that helps you make more pee to get rid of excess water inyour body. A healthcare provider will give you this injection in ahospital or clinic setting. It treats swelling from heart, kidney or liverdisease or swelling around your brain or in your eyes.

Superior Purity and Quality Assurance

Mannitol BP/USP is manufactured to meet both BP and USP standards, guaranteeing a purity of 97.0% to 102.0%. Every batch is precisely analyzed to ensure compliance with global pharmaceutical requirements, assuring quality for every application.

Optimal Physical Properties for Diverse Applications

Its white crystalline powder form, stable solubility, and defined melting point (167170 C) make Mannitol BP/USP an adaptable ingredient in pharmaceutical formulations, meeting the technical needs of various drug delivery systems.

Reliable Shelf Life and Storage Stability

With a shelf life of five years, Mannitol BP/USP provides consistent performance over extended periods. Proper storage in dry conditions further ensures its stability, making it a trustworthy choice for manufacturers and suppliers.

FAQs of Mannitol BP/USP:

Q: How is Mannitol BP/USP typically used in pharmaceutical applications?

A: Mannitol BP/USP serves as an excipient, diluent, and osmotic diuretic in pharmaceutical products, aiding in tablet formulation and drug delivery due to its stability, solubility, and safety profile.

Q: What are the benefits of using Mannitol BP/USP in drug manufacturing?

A: Its high purity, stable physical properties, and excellent solubility in water contribute to efficient drug formulation, enhancing product consistency and patient safety.

Q: When should Mannitol BP/USP be stored and used following receipt from the supplier?

A: Mannitol BP/USP should be stored immediately in a dry place upon receipt, away from oxidizing agents, and used within its five-year shelf life for optimal effectiveness.

Q: Where is Mannitol BP/USP produced and supplied from?

A: Mannitol BP/USP is manufactured, exported, and supplied by reliable producers based in India, ensuring global availability for pharmaceutical manufacturers.

Q: What is the recommended process for incorporating Mannitol BP/USP into a pharmaceutical formulation?

A: Begin by verifying its appearance and purity, then dissolve Mannitol in water as needed during the formulation process, ensuring compatibility with other ingredients and avoiding strong oxidizing agents.

Q: Is Mannitol BP/USP suitable for industrial applications beyond pharmaceuticals?

A: Yes, Mannitol BP/USP can be used in industrial-grade applications, leveraging its chemical stability and physical characteristics for processes beyond pharmaceuticals, as specified by its grade.

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