Rosuvastatin Impurity NEW

Professional R&D, Quality Assurance

Our R&D team boasts years of experience in developing Rosuvastatin impurity reference standards, dedicated to providing customers with the highest quality products. Through rigorous quality control testing, we ensure that each batch meets international standards and customer requirements.

Comprehensive Services, Meeting Needs

Beyond providing high-quality Rosuvastatin impurity reference standards, we also offer comprehensive service support. From product consultation, purchasing guidance, to after-sales support, we always put customers first, meeting your various needs.

All of our products include a complete set of structural confirmation maps. Such as COA, H-NMR,MASS,HPLC,UV,IR。The default HPLC purity of our products is not less than 95%. Particularly unstable products have a purity of no less than 90% and will be communicated to the customer in advance. we can also provide TGA,Q-NMR,C-NMR and so on。