Rosuvastatin Impurity NEW

$0.00 10mg

$0.00 30mg

$0.00 100mg

Min. Order10mg
Purity98%+
Cas No1714147-47-3
Supply Ability20g
Update time2025-01-03

Moxin Chemicals

1YR

China

Since2022-11-29

AddressRoom 005-01, 15th Floor, Building D2, Phase III, Software New Town, No. 8 Huacheng Avenue, East Lake

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Chemical Properties

Product Name	Rosuvastatin Impurity
CAS No	1714147-47-3
EC-No
Min. Order	10mg
Purity	98%+
Supply Ability	20g
Release date	2025/01/03

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。

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Company Profile Introduction

1. Drug standards and drug impurity reference substances: provide more than 20,000 kinds of spot impurity reference substances, with sufficient supply and same-day delivery. We have a professional R&D team and comprehensive quality control testing to ensure product quality and reliability. 2. Customized synthesis of impurities and new molecules: Quickly respond to the customized needs of CDE impurities, stably supply impurities that have established quality standards, and provide customized synthesis services for new compounds in the research and development of innovative drugs. 3. Preparation and separation of unknown impurities: With a professional impurity preparation and separation technical team and SFC preparation and separation instruments, we can solve the problems of impurity preparation in complex projects. 4. Process development of new drug intermediates: provide the supply of new drugs and new molecular impurities, process optimization services, as well as the screening and impurity analysis of commercialization routes. 5. Peptide synthesis: Provide customized peptide synthesis services, and cover all kinds of degradation impurities and process impurities generated in the research and development of peptide drugs. At the same time, it provides comprehensive structural confirmation data and customized testing services.