Capecitabine is a widely prescribed oral chemotherapy medication used to treat various cancers, including breast, colorectal, and gastric cancers. Its efficacy relies on its conversion within the body to 5-fluorouracil (5-FU), a potent antimetabolite that interferes with DNA synthesis in cancer cells. The synthesis of Capecitabine is a complex process, and the quality of its pharmaceutical intermediates is paramount to ensure the purity, safety, and efficacy of the final drug product. For manufacturers, identifying reliable suppliers for key intermediates is a critical strategic decision.
The Importance of 2',3'-Di-O-acetyl-5'-deoxy-5-fluorocytidine in Capecitabine Synthesis
Among the critical intermediates in Capecitabine production is 2',3'-Di-O-acetyl-5'-deoxy-5-fluorocytidine (CAS 161599-46-8). This acetylated and fluorinated cytidine derivative serves as a foundational component in creating the Capecitabine molecule. The presence of specific functional groups and the overall stereochemistry are crucial. Therefore, sourcing this intermediate with stringent purity specifications is non-negotiable for pharmaceutical manufacturers aiming for consistent and compliant API production. A high assay value, such as that offered by NINGBO INNO PHARMCHEM CO.,LTD. (≥99.0%), directly translates to a cleaner synthesis and a higher yield of the desired API.
Why Choose a Reputable Manufacturer?
The consequences of using impure or substandard intermediates can be severe, leading to:
As a leading chemical supplier in China, NINGBO INNO PHARMCHEM CO.,LTD. is dedicated to providing pharmaceutical intermediates that meet the highest standards. Our commitment to quality control, combined with competitive pricing and efficient supply chain management, makes us a preferred partner for companies looking to buy 2',3'-Di-O-acetyl-5'-deoxy-5-fluorocytidine and other vital intermediates.
Key Considerations When Sourcing
When procuring Capecitabine intermediates, consider the following:
Investing in high-quality pharmaceutical intermediates is an investment in the integrity of your final product and, ultimately, in patient safety. NINGBO INNO PHARMCHEM CO.,LTD. is committed to supporting your manufacturing needs with reliable, high-purity chemical solutions.
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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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