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Postion:Product Catalog >N-Nitroso LCZ696
N-Nitroso LCZ696
  • N-Nitroso LCZ696
  • N-Nitroso LCZ696
  • N-Nitroso LCZ696

N-Nitroso LCZ696 NEW

Price Get Latest Price
Package 10mg 30mg 100mg
Min. Order: 10mg
Supply Ability: 100000
Update Time: 2025-01-21

Product Details

Product Name: N-Nitroso LCZ696 CAS No.: 2254485-68-0
Min. Order: 10mg Purity: 95%+
Supply Ability: 100000 Release date: 2025/01/21
N-Nitroso LCZ696   CAS:2254485-68-0
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The Sacubitril Valsartan Impurity Reference Standard is an essential reagent in drug research and development, as well as quality control. It is used to verify and detect the impurity content in Sacubitril Valsartan drugs, ensuring the quality and safety of the medication. Our Sacubitril Valsartan Impurity Reference Standard is carefully prepared and undergoes rigorous quality control, ensuring high purity and stability.


This reference standard is suitable for various analytical techniques, such as High-Performance Liquid Chromatography (HPLC), Nuclear Magnetic Resonance (NMR), and Mass Spectrometry (MS), to meet the needs of different laboratories. By using our Sacubitril Valsartan Impurity Reference Standard, you can accurately identify and quantify impurities in the drug, providing reliable data support for drug research and development, production, and quality control.

Please note that this product is intended for research and industrial production use only and should not be used for human treatment or diagnosis. Store the product according to the instructions on the packaging to ensure its stability and effectiveness.


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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.

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