Letermovir Intermediate (CAS 917389-30-1) | High-Performance Building Block for Antiviral API Synthesis
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🔬 Product Overview
Letermovir Intermediate (CAS 917389-30-1) is a pivotal chemical intermediate in the synthesis of Letermovir, a novel antiviral agent targeting cytomegalovirus (CMV) infections, particularly in immunocompromised patients (e.g., transplant recipients). This intermediate ensures efficient, scalable production of Letermovir API while adhering to stringent pharmaceutical quality standards.
Primary Function: Enables high-yield, impurity-controlled synthesis of Letermovir API.
Applications: Antiviral drug manufacturing, CMV therapy R&D, generic drug development.
✅ Key Advantages
⭐ Ultra-High Purity
⚙️ Process Optimization
🌡️ Robust Stability
📜 Regulatory Ready
📋 Applications
API Production: Core precursor in Letermovir API synthesis for CMV prophylaxis and treatment.
Generic Antiviral Drugs: Supports cost-effective alternatives to branded CMV therapies.
Antiviral Research: Used to develop next-generation CMV inhibitors with improved resistance profiles.
Clinical Trial Materials: Critical for scaling batches in pre-clinical and Phase I-III studies.
🏅 Quality Certifications
Rigorously tested via HPLC, NMR, LC-MS, and GC (aligned with ICH/USP/EP protocols).
Comprehensive Certificate of Analysis (CoA) includes impurity profiles, spectral data, and chromatograms.
🌐 Market Trends
The global CMV treatment market is projected to grow at 5.8% CAGR (2024-2028), fueled by increasing organ transplant rates and demand for targeted antiviral therapies like Letermovir. Intermediate suppliers are pivotal in meeting API production needs, especially in regions with expanding access to post-transplant care (e.g., Asia-Pacific and North America).
🔍 Why Choose Us?
Custom Synthesis: Flexible purity grades (98%-99.9%) and batch sizes (grams to kilograms).
Reliable Supply Chain: Temperature-controlled logistics with real-time tracking and regulatory documentation.
Technical Support: End-to-end assistance in process optimization, impurity control, and regulatory filings.
China
