Quinine Sulphate BP-USP-EP

Quinine Sulphate BP-USP-EP Specification

Solubility
It is freely soluble in acetic acid (100), slightly soluble in water

Melting Point
234C

Molecular Weight
746.912 [g/mol]

Ph Level
2.5

Molecular Formula
2(C20H24N2O2).H2SO4

Storage
Dry Place

Loss on Drying
8.0%

Medicine Name
Pharma garde

Chemical Name
6-methoxy-cinchonan-9-o (8alpha, 9theta)-cinchonan-9-osulfate(2:1)(salt)

CAS No
804-63-7

Type
Pharmaceutical Intermediates

Grade
Industrial Grade

Usage
Pharmaceutical

Purity(%)
99.2%

Appearance
white crystals or crystalline powder

Physical Form
Powder

Quinine Sulphate BP-USP-EP Trade Information

Minimum Order Quantity
10 Kilograms

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

About Quinine Sulphate BP-USP-EP

It is used to treat malaria caused by Plasmodium falciparum. Plasmodium falciparum is a parasite that getsinto the red blood cells in the body and causes malaria. Quinine works bykilling the parasite or preventing it from growing.

Exceptional Quality and Compliance

Quinine Sulphate BP-USP-EP is manufactured to meet stringent pharmaceutical standards, ensuring high-quality purity (99.2%) and compliance with BP, USP, and EP descriptors. The careful control of loss on drying and solubility parameters guarantees reliable performance in various pharmaceutical applications.

Ideal for Pharmaceutical Manufacturing

With its well-defined crystalline appearance and precise chemical characteristics, Quinine Sulphate BP-USP-EP is a trusted intermediate for pharmaceutical companies. Its consistent performance supports efficient drug synthesis, particularly in the formulation of anti-malarial treatments and similar medications.

Optimized Handling and Storage

This product is designed for stability, requiring storage in a dry environment to maintain its quality. Its industrial-grade specification allows for safe and effective handling in manufacturing settings, making it suitable for exporters, suppliers, and manufacturers across global markets.

FAQs of Quinine Sulphate BP-USP-EP:

Q: How should Quinine Sulphate BP-USP-EP be stored for maximum stability?

A: Quinine Sulphate BP-USP-EP should be stored in a dry place to prevent moisture absorption, which can affect its crystalline structure and purity. Following proper storage conditions helps retain its pharmaceutical integrity.

Q: What are the primary uses of Quinine Sulphate BP-USP-EP in the pharmaceutical industry?

A: This compound is mainly used as an intermediate in pharmaceutical manufacturing, particularly in the synthesis of drugs such as anti-malarial medications. Its high purity and compliance with international standards make it suitable for critical medical applications.

Q: When should Quinine Sulphate BP-USP-EP be used during the pharma production process?

A: Quinine Sulphate BP-USP-EP is typically incorporated during the intermediate stages of pharmaceutical synthesis where precision and reliability are essential for the final products efficacy.

Q: Where is Quinine Sulphate BP-USP-EP manufactured and supplied from?

A: It is manufactured, exported, and supplied from India, a leading hub for pharmaceutical intermediates that ensures competitive quality and regulatory compliance for international markets.

Q: What benefits does using high-purity Quinine Sulphate BP-USP-EP provide?

A: Utilizing a product with 99.2% purity minimizes impurities, enhancing drug safety, consistency, and effectiveness. This translates to better patient outcomes and manufacturing efficiency.

Q: What is the process for checking the solubility of Quinine Sulphate BP-USP-EP?

A: To test its solubility, labs typically use acetic acid (where it is freely soluble) or water (where solubility is limited), verifying it matches specifications crucial for pharmaceutical use.

Q: How is Quinine Sulphate BP-USP-EP typically used by exporters, manufacturers, and suppliers?

A: Companies utilize it as a key pharmaceutical intermediate or raw material in bulk drug production, ensuring the quality supply of active ingredients for finished medications across global markets.

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