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Dihydroxy Diketo Atorvastatin Impurity drug impurities drug standards
Our products are mainly drug impurity reference products, drug standards, analytical chemistry, standard substances, organic chemical synthesis, chemical custom synthesis. For impurity localization, quantification, and quality control in drug development processes. Our laboratory area is more than 5000 square meters, we have more than 20 analytical instruments such as HPLC and MS/LC-MS/GC-MS, we also have TGA, IR and other testing instruments. We have the most advanced SFC preparation separation equipment. We can provide a full range of impurity reference/standard products required for drug development. Most of the impurities are synthesized through the process, there are also many items of impurities can not be obtained by synthetic means, need to be obtained through raw materials, intermediates, crude products or side reactions contained in the trace target compounds, Hubei Moke has a professional impurity preparation and separation technology team, equipped with professional SFC preparation and separation equipment. It can carry out efficient and accurate separation of impurities for complex projects, and solve the problem of impurity preparation for customers.
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。
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