Valsartan USP

Valsartan USP Specification

Molecular Weight
435.5188 g/mol

Molecular Formula
C24H29N5O3

Storage
Dry Place

Melting Point
116-117

Boiling point
684.9

Shelf Life
3 Years

Medicine Name
Valsartan

Chemical Name
(2S)-3-methyl-2-[N-({4-[2-(2H-1,2,3,4-tetrazol-5-yl)phenyl]phenyl}methyl)pentanamido]butanoic acid

CAS No
137862-53-4

Type
Pharmaceutical Intermediates

Grade
Medicine Grade

Usage
Pharmaceutical

Purity(%)
99.0%

Appearance
White crystalline powder

Physical Form
Powder

Valsartan USP Trade Information

Minimum Order Quantity
50 Kilograms

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

About Valsartan USP

Valsartan is used alone or together with other medicines to treat high blood pressure (hypertension). High blood pressure adds to the workload of the heart and arteries. If it continues for a long time, the heart and arteries may not function properly. This can damage the blood vessels of the brain, heart, and kidneys, resulting in a stroke, heart failure, or kidney failure. Lowering blood pressure can reduce the risk of strokes and heart attacks. Valsartan is also used to treat heart failure and left ventricular failure after a heart attack. Left ventricular failure occurs when the left side of the heart (the main pumping chamber) becomes stiff and enlarged or swollen. This causes pooling of blood in the lungs because the heart is not pumping properly.

Premium Quality and Compliance

Our Valsartan USP is characterized by high purity (99.0%) and conforms to medicine grade standards, making it highly reliable for pharmaceutical preparations. The compounds strict quality control ensures it meets international regulatory requirements, suitable for exporters, manufacturers, and suppliers.

Key Properties and Chemical Profile

Valsartan USP is provided as a white crystalline powder with a melting point of 116-117C and a boiling point of 684.9C. It features a robust molecular profile, comprising C24H29N5O3 with a molecular weight of 435.5188 g/mol. This ensures consistency and efficacy across various pharmaceutical processes.

Usage and Benefits in Medicine

Primarily used as a pharmaceutical intermediate, Valsartan plays a vital role in the formulation of medicines for treating high blood pressure. Its stable shelf life (3 years) and ultra-pure quality support reliable drug manufacturing, while its well-defined structure aids in targeted therapeutic applications.

FAQs of Valsartan USP:

Q: How should Valsartan USP be stored to maintain its quality?

A: Valsartan USP should be stored in a dry place to prevent moisture absorption and degradation, thus preserving its stability and efficacy throughout its three-year shelf life.

Q: What are the typical applications of Valsartan USP in pharmaceuticals?

A: Valsartan USP is predominantly used as an intermediate in the production of antihypertensive medications, particularly for managing high blood pressure and supporting cardiovascular health.

Q: When is it appropriate to use Valsartan USP in drug manufacturing?

A: Valsartan USP is incorporated during the synthesis phase of medicine production, where its pure, stable form ensures optimal reaction outcomes and compliant formulations.

Q: Where does the supply of Valsartan USP originate from?

A: This product is manufactured, exported, and supplied from India, adhering to international pharmaceutical industry standards.

Q: What is the process for obtaining Valsartan USP for research or commercial production?

A: Valsartan USP can be ordered through authorized pharmaceutical suppliers and exporters in India who provide documentation on purity, grading, and regulatory compliance.

Q: What are the benefits of using medicine-grade Valsartan USP?

A: Medicine-grade Valsartan USP guarantees high purity, safety, and consistency, which are critical for effective drug formulation and safe therapeutic outcomes for end users.

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