Custom Manufacturing, Project Outsourcing, your Trusted Partner from China
In the pharmaceutical industry, the adage 'quality in, quality out' is never more critical than when dealing with chemical intermediates. For 3-Pyridylacetic Acid (CAS No. 501-81-5), a key intermediate in the synthesis of Risedronic acid, adhering to stringent purity standards is not just a best practice but a necessity. NINGBO INNO PHARMCHEM CO.,LTD. places paramount importance on delivering intermediates that meet and exceed these rigorous requirements.
The primary application of 3-Pyridylacetic Acid is in the synthesis of Risedronic acid, a medication widely used to treat osteoporosis. The efficacy and safety of Risedronic acid directly depend on the purity of its constituent parts. Therefore, the assay specification for 3-Pyridylacetic Acid, commonly stated as ≥99.0%, is a critical benchmark. This high purity ensures that unwanted side products or contaminants are minimized, which is essential for regulatory compliance and for ensuring the therapeutic effectiveness of the final API.
When pharmaceutical manufacturers look to buy 3-pyridylacetic acid, they are not just purchasing a chemical compound; they are investing in the quality assurance of their own products. Consistent batch-to-batch purity of this pyridine derivative is vital for reproducible manufacturing processes. Suppliers like NINGBO INNO PHARMCHEM CO.,LTD. implement robust quality control measures to guarantee that each delivery of 3-Pyridylacetic Acid meets the specified purity levels, thereby supporting the integrity of the Risedronate synthesis pathway.
The chemical properties of 3-pyridylacetic acid, including its stability and handling characteristics, are also closely monitored to maintain purity. Proper storage and packaging are crucial to prevent degradation. By prioritizing these quality aspects, NINGBO INNO PHARMCHEM CO.,LTD. ensures that its clients receive a product that is ready for immediate use in demanding pharmaceutical manufacturing environments. This dedication to purity is fundamental to our commitment to supporting the global healthcare sector.
Manufacturing Facilities
Professional Export Experience
to Global Customers
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).
A: We don't have Minimum Order Quantity, exact quantity should be provided before quotation for us to calculate the exact cost.
A: We don't provide free samples due to lots of request and expensive international courier's cost, we can deduct the sample charge after commercial order placed.
A: Our payment terms: Small or sample order: T/T IN ADVANCE. Commercial order: First order should be by T/T IN ADVANCE or L/C at sight, and following orders T/T 30~90days is acceptable subject to approval of credit application.
