Dehydro Ivabradine: Synthesis, Analysis, and Pharmaceutical Applications
A deep dive into the critical pharmaceutical intermediate and impurity, Dehydro Ivabradine, exploring its synthesis, analytical methods, and role in drug quality.
Get a Quote & SampleProduct Core Value
Dehydro Ivabradine
Dehydro Ivabradine (CAS 1086026-31-4) is a pivotal pharmaceutical intermediate and a significant process-related impurity in the synthesis of Ivabradine. Its accurate detection and control are paramount for ensuring the quality, safety, and efficacy of Ivabradine-based medications, particularly those used in cardiovascular treatments.
- Pharmaceutical Intermediate Synthesis and Analysis: This compound is a key precursor in the synthesis of Ivabradine, making its own synthesis and characterization crucial for downstream drug production. Understanding the pharmaceutical intermediate synthesis and analysis is vital for efficient manufacturing.
- Cardiovascular Drug Development Insights: As a compound related to Ivabradine, a heart rate-lowering medication, Dehydro Ivabradine is relevant to broader cardiovascular drug development insights. Research into its properties aids in understanding drug action and safety.
- Pharmaceutical Impurity Profiling Techniques: The presence of Dehydro Ivabradine as an impurity necessitates robust pharmaceutical impurity profiling techniques. Advanced analytical methods are employed to detect and quantify it accurately.
- Advances in HPLC for Pharmaceutical Quality: The precise quantification of Dehydro Ivabradine often relies on advanced HPLC methods, showcasing advances in HPLC for pharmaceutical quality. These methods ensure that drug products meet stringent purity standards.
Key Advantages
Enhanced Purity Control
Accurate quantification of Dehydro Ivabradine through sophisticated analytical techniques ensures higher purity levels in final pharmaceutical products, directly impacting patient safety.
Streamlined Synthesis Pathways
Understanding the synthesis of Dehydro Ivabradine provides pathways for optimizing the production of Ivabradine, potentially leading to cost efficiencies and improved yields in pharmaceutical manufacturing process optimization.
Reliable Quality Assurance
As a critical reference standard, Dehydro Ivabradine supports the development and validation of stability-indicating methods, bolstering reliable quality assurance in drug manufacturing.
Key Applications
Pharmaceutical Synthesis
Serves as a vital intermediate in the synthesis of Ivabradine and related cardiovascular drugs, highlighting its importance in pharmaceutical synthesis.
Impurity Analysis
Crucial for developing and validating analytical methods to detect and quantify impurities in Ivabradine, contributing to stringent quality control measures.
Research and Development
Used in preclinical studies to understand drug mechanisms, degradation pathways, and to support drug development processes, offering valuable cardiovascular drug development insights.
Quality Control Standard
Essential as a reference standard for ensuring product quality and compliance with regulatory guidelines in the pharmaceutical industry, demonstrating pharmaceutical intermediate quality control.