Amlodipine Besylate BP-USP-EP

Amlodipine Besylate BP-USP-EP Specification

Loss on Drying
0.5%

Melting Point
195 204 C

Solubility
Slightly soluble in water, soluble in methanol

Shelf Life
2 Years

Storage
Dry Place

Heavy Metal (%)
10 ppm

Molecular Formula
C20H25ClN2O5 C6H6O3S

Molecular Weight
567.05 Grams (g)

Medicine Name
Amlodipine Besylate

Chemical Name
3-Ethyl 5-methyl (4RS)-2-[(2-aminoethoxy)methyl]-4-(2-chlorophenyl)-6-methyl-1,4-dihydropyridine-3,5-dicarboxylate benzenesulfonate

CAS No
111470-99-6

Type
Other

Grade
Industrial Grade

Usage
Antihypertensive drug manufacturing / Pharmaceutical formulations

Purity(%)
99.0% (HPLC)

Appearance
White or almost white crystalline powder

Physical Form
Powder

Amlodipine Besylate BP-USP-EP Trade Information

Minimum Order Quantity
25 Kilograms

Delivery Time
1 Week

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