In the dynamic landscape of pharmaceutical manufacturing, the availability of high-quality intermediates is paramount to the successful development and production of active pharmaceutical ingredients, or APIs. These crucial building blocks underpin the efficacy, safety, and purity of final drug products. Among these vital components, Fexuprazan Impurity 1, identified by its CAS No. 1902955-29-6, stands out as a particularly significant pharmaceutical intermediate. NINGBO INNO PHARMCHEM CO.,LTD. is proud to be a dedicated provider of this essential compound, ensuring the robust supply chain required by the global pharmaceutical industry.
Fexuprazan Impurity 1, also known by its systematic chemical name Methyl 5-(2,4-Difluorophenyl)-4-Methoxy-1H-Pyrrole-3-Carboxylate, plays a pivotal role in the synthesis of Fexuprazan. Fexuprazan itself is a groundbreaking potassium-competitive acid blocker (P-CAB), representing a new generation of drugs designed for the treatment of acid-related gastrointestinal disorders, such as gastroesophageal reflux disease (GERD). The development of such advanced therapeutic agents necessitates intermediates of impeccable quality and consistent availability, which is precisely what NINGBO INNO PHARMCHEM CO.,LTD. strives to deliver.
The chemical structure of Fexuprazan Impurity 1, with its formula C13H11F2NO3 and molecular weight of 267.23, is meticulously engineered to serve as a critical precursor. Its precise composition ensures the correct molecular scaffolding is in place for subsequent reactions in the Fexuprazan synthesis pathway. As a white powder with a purity exceeding 98%, this intermediate meets stringent pharmaceutical standards, guaranteeing its suitability for sensitive drug manufacturing processes. Predictive physical properties, such as a boiling point around 409.4±45.0 °C and a density of approximately 1.314±0.06 g/cm3, further highlight its well-defined chemical profile, crucial for process control and scalability in pharmaceutical production.
The applications of Fexuprazan Impurity 1 extend beyond its primary use as a synthetic intermediate. Due to its well-characterized nature and high purity, it is also invaluable in various aspects of pharmaceutical research and development. It serves as a critical reference standard for impurity profiling and quality control in the manufacturing of Fexuprazan. Researchers rely on such analytical reagents for precise PRO analysis and for synthesis experiments in laboratory settings, ensuring that future drug candidates are developed with the highest level of accuracy and safety. Its role as a benchmark for impurity levels during the drug substance manufacturing process is indispensable for compliance with regulatory guidelines and for safeguarding patient well-being.
Maintaining strict control over impurities like Fexuprazan Impurity 1 throughout the synthesis process is a cornerstone of pharmaceutical quality assurance. Even trace amounts of unintended by-products can significantly impact the safety, efficacy, and stability of the final API. Therefore, procuring this intermediate from a reputable source, one that emphasizes rigorous analytical testing and quality management systems, becomes an absolute imperative for drug developers and manufacturers. NINGBO INNO PHARMCHEM CO.,LTD. employs state-of-the-art analytical techniques to ensure the consistent purity and quality of Fexuprazan Impurity 1, minimizing risks for our clients and supporting their regulatory compliance efforts globally.
NINGBO INNO PHARMCHEM CO.,LTD. understands the critical importance of reliable supply and uncompromising quality in the pharmaceutical sector. Our manufacturing processes for Fexuprazan Impurity 1 are designed to meet rigorous international quality standards, reflecting our commitment to excellence. We adhere to principles that align with global benchmarks such as GMP (Good Manufacturing Practices), ISO 9001, and FDA guidelines, ensuring that every batch of this intermediate is produced under controlled conditions, traceable, and consistent. This dedication to quality control ensures that our partners can proceed with their synthesis work with complete confidence in the integrity of their raw materials.
The global demand for innovative therapeutic solutions continues to grow, placing increasing pressure on pharmaceutical companies to accelerate drug development cycles while maintaining the highest quality. Fexuprazan, as a highly anticipated P-CAB, is poised to make a significant impact on the treatment of acid-related disorders. The efficient and reliable supply of its key intermediates, like Fexuprazan Impurity 1, is therefore not just a logistical necessity but a strategic advantage for manufacturers aiming to bring these vital medicines to market. NINGBO INNO PHARMCHEM CO.,LTD. is positioned as a dependable partner in this endeavor, providing the foundational chemical building blocks necessary for therapeutic breakthroughs. Our robust production capacity ensures that we can meet both current and future market demands, providing a stable supply even for large-scale pharmaceutical operations.
Our commitment extends beyond simply providing a product; we aim to foster long-term partnerships built on trust and mutual success. For those looking to secure a consistent supply of this critical intermediate, NINGBO INNO PHARMCHEM CO.,LTD. is a premier manufacturer and supplier of Fexuprazan Impurity 1 (CAS 1902955-29-6). We invite inquiries regarding our product specifications and competitive price structures. Companies seeking to buy or purchase this high-quality pharmaceutical intermediate can easily reach out to our dedicated sales team. We offer detailed product documentation, comprehensive technical support, and a commitment to customer satisfaction, ensuring a seamless procurement process. Whether you require small quantities for research and development or large volumes for commercial production, NINGBO INNO PHARMCHEM CO.,LTD. is equipped to meet your needs with efficiency and professionalism. Our global distribution network ensures timely delivery, helping our clients maintain their production schedules without interruption. Partner with NINGBO INNO PHARMCHEM CO.,LTD. for your Fexuprazan intermediate requirements and experience the assurance of quality, reliability, and dedicated customer service. We are committed to contributing to the advancement of global health through our unparalleled expertise in pharmaceutical intermediate supply.
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1. 20 years of R&D, manufacturing and sales experience, serving customers in 60 countries and regions around the world;
2. Own R&D laboratory, pilot platform and large-scale production workshop, which can meet the audit requirements of global customers;
3. We can satisfy customers' perfect transition from small scale lab requirements (gram level) to commercialization requirements (hundred tons level).
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