Ramipril API

Ramipril API Specification

Storage
Dry Place

Shelf Life
5 Years

Molecular Weight
416.52

Molecular Formula
C23H32N2O5

Medicine Name
Ramipril

Chemical Name
Tritace, [2S,3aS,6aS]-1-[(2S)-2-[[(1S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-1-oxopropyl]octahydrocyclopenta[b]pyrrole-2-carboxylic acid

Type
Pharmaceutical Intermediates

Grade
Industrial Grade

Usage
Pharmaceutical and Anti-hypertension drugs.

Purity(%)
99.5%min

Appearance
white or off-white crystalline powder

Physical Form
Powder

Ramipril API 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 Ramipril API

Ramipril is in a class ofmedications called angiotensin-converting enzyme (ACE) inhibitors. Itworks by decreasing certain chemicals that tighten the blood vessels, so bloodflows more smoothly and the heart can pump blood more efficiently.

Superior Quality & Stability

Ramipril API is manufactured to industrial-grade standards and offers exceptional purity at a minimum of 99.5%. Its crystalline powder form ensures ease of use in pharmaceutical formulations. The product is supplied with a shelf life of five years when stored correctly in a dry place, underpinning lasting stability and performance.

Core Applications & Benefits

This API is most commonly found in the production of anti-hypertension drugs, providing clinicians and patients with a reliable ingredient for blood pressure management. Its high level of purity and well-defined molecular structure guarantee consistent therapeutic outcomes while meeting rigorous industry standards.

FAQs of Ramipril API:

Q: How should Ramipril API be stored to maintain its efficacy?

A: Ramipril API should be stored in a dry place and away from direct moisture to preserve its purity and effectiveness throughout its five-year shelf life.

Q: What is the primary usage of Ramipril API in the pharmaceutical industry?

A: Ramipril API is predominantly used in the formulation of anti-hypertension medications, helping in the management and treatment of high blood pressure.

Q: When should Ramipril API be considered for pharmaceutical manufacturing?

A: It should be considered during the production of pharmaceutical products requiring reliable and pure anti-hypertensive compounds, notably when high purity (99.5% min) and extended shelf life are prerequisites.

Q: Where is Ramipril API typically manufactured and supplied from?

A: This pharmaceutical intermediate is primarily manufactured, exported, and supplied from India, catering to global pharmaceutical requirements.

Q: What is the process for utilizing Ramipril API in drug formulation?

A: The crystalline powder form of Ramipril API allows for straightforward integration in drug formulations, ensuring precise dosing and consistent batch quality during production.

Q: What are the key benefits of using Ramipril API in medicinal products?

A: The key benefits include high purity, proven anti-hypertensive efficacy, long storage stability, and compliance with stringent pharmaceutical industry requirements.

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