Trityl Losartan CAS 133909-99-6: A Key Intermediate for Losartan Impurity Profiling and Pharmaceutical Synthesis
Essential chemical intermediate and reference standard for pharmaceutical synthesis and quality control of Losartan.
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Trityl Losartan
Trityl Losartan, identified by CAS number 133909-99-6, is a critical chemical compound primarily utilized as an intermediate in the synthesis of Losartan and in the profiling of its impurities. Its precise molecular structure (C41H37ClN6O) and well-defined physical properties, such as being a white solid, make it an indispensable tool in pharmaceutical research and development.
- Facilitating Losartan impurity synthesis: This compound plays a vital role in creating and identifying impurities associated with Losartan, crucial for regulatory compliance.
- Serving as a pharmaceutical intermediate: It is a key building block in the complex chemical synthesis pathways leading to active pharmaceutical ingredients (APIs) like Losartan.
- Ensuring Losartan quality control standard: As a reference standard, it allows for accurate testing and validation of Losartan's purity and quality during manufacturing.
- Supporting N-Trityl Losartan impurity profiling: Its availability aids researchers in understanding and managing potential N-Trityl Losartan impurities within pharmaceutical products.
Key Advantages
Precision in Synthesis
Leverage Trityl Losartan for precise chemical synthesis, ensuring the accurate production of Losartan and its related compounds.
Robust Quality Assurance
Utilize this compound as a pharmaceutical intermediate to uphold stringent quality control standards in drug manufacturing.
Regulatory Compliance Aid
Employ Trityl Losartan in impurity profiling to meet regulatory requirements and ensure product safety and efficacy.
Key Applications
Pharmaceutical Synthesis
Acts as a crucial intermediate in the manufacturing processes of Losartan, contributing to the production of essential medications.
Impurity Profiling
Essential for identifying and quantifying impurities in Losartan formulations, ensuring product purity and safety.
Reference Standards
Serves as a vital reference standard for analytical testing and quality assurance in the pharmaceutical industry.
Research and Development
Supports R&D efforts, including ANDA filings and toxicity studies, by providing a reliable chemical for experimentation.