Amlodipine Besylate BP-USP-EP

Amlodipine Besylate BP-USP-EP Specification

Storage
Dry Place

Molecular Formula
C26H31ClN2O8S

Boiling point
527.2 C at 760 mmHg

Molecular Weight
567.1

Solubility
Slightly soluble in water and in 2-propanol,Freely Soluble in methanol, sparingly soluble in ethanol.

Loss on Drying
0.5%

Melting Point
195-204 C

Medicine Name
Amlodipine

Type
Pharmaceutical Intermediates

Grade
Industrial Grade

Usage
Pharmaceutical

Purity(%)
97.0%-102.0%

Appearance
White or almost white powder.

Physical Form
Powder

Amlodipine Besylate 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 Amlodipine Besylate BP-USP-EP

It lowers blood pressure by relaxing the bloodvessels so the heart does not have to pump as hard. It controls chest pain by increasing the supplyof blood to the heart. If taken regularly, amlodipine controls chest pain, butit does not stop chest pain once it starts.

Industrial Grade Quality

Amlodipine Besylate BP-USP-EP is produced to meet industrial grade standards, ensuring reliable quality for pharmaceutical applications. Its high purity and controlled loss on drying support consistent performance in drug manufacturing processes, making it a trusted choice for global buyers.

Pharmaceutical Application

As a key intermediate, Amlodipine Besylate BP-USP-EP plays a vital role in the synthesis of medications for hypertension and cardiovascular disorders. Its compatibility with various solvents allows for flexible integration in different production setups, supporting efficient formulation and processing.

FAQs of Amlodipine Besylate BP-USP-EP:

Q: How should Amlodipine Besylate BP-USP-EP be stored to maintain its quality?

A: Amlodipine Besylate BP-USP-EP should be stored in a dry place to prevent moisture-induced degradation and preserve its purity and physical form.

Q: What is the typical physical appearance of Amlodipine Besylate BP-USP-EP?

A: This intermediate is characterized by its white or almost white powder form, facilitating easy handling and mixing during pharmaceutical production.

Q: When is Amlodipine Besylate BP-USP-EP used in the pharmaceutical manufacturing process?

A: Amlodipine Besylate BP-USP-EP is utilized during the synthesis phase of antihypertensive medications, providing essential active ingredients for further formulation.

Q: Where is Amlodipine Besylate BP-USP-EP sourced from?

A: It is produced, exported, and supplied by manufacturers in India, ensuring global distribution to pharmaceutical companies and intermediaries.

Q: What process is recommended for integrating Amlodipine Besylate BP-USP-EP into pharmaceutical formulations?

A: Due to its solubility profile, it is typically dissolved in methanol or utilized in processes compatible with its limited water solubility to ensure uniformity in the final product.

Q: What are the primary benefits of using industrial grade Amlodipine Besylate BP-USP-EP?

A: Using this industrial grade intermediate supports high product purity (97.0%102.0%), consistency in batch production, and compliance with BP, USP, and EP standards.

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