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Postion:Product Catalog >Amlodipine Nitroso Impurity 66
Amlodipine Nitroso Impurity 66
  • Amlodipine Nitroso Impurity 66
  • Amlodipine Nitroso Impurity 66
  • Amlodipine Nitroso Impurity 66
  • Amlodipine Nitroso Impurity 66

Amlodipine Nitroso Impurity 66 NEW

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Package 5mg 20mg 50mg
Min. Order: 1mg
Supply Ability: 10000
Update Time: 2025-07-31

Product Details

Product Name: Amlodipine Nitroso Impurity 66 Min. Order: 1mg
Purity: >95% HPLC Supply Ability: 10000
Release date: 2025/07/31
Molecular Formula:: C20H19ClN2O6 Mol. Weight:: 418.83
Appearance: : Pale yellow soild


Article illustration

Product Catalog:A004066
CAS No.:
Product Name:Amlodipine Nitroso Impurity 66
Purity:>95% HPLC
Synonyms: 5-ethyl 7-methyl 6-(2-chlorophenyl)-8-methyl-4-nitroso-3,4-dihydro-2H-benzo[b][1,4]oxazine-5,7-dicarboxylate
Molecular Formula:C20H19ClN2O6
Mol. Weight:418.83
Appearance: Pale yellow soild
Storage:2-8°C Refrigerator
Contact:WhatsAPP: +86 17320513646
E-mail: anna@molcoo.com
Note:We can also customize related analogues and modified peptides including HPLC, MS, 1H-NMR, MS, HPLC, IR, UV, COA, MSDS.
This product is intended for laboratory use only!
Background:Amlodipine is a widely used drug for treating hypertension and coronary heart disease. The Amlodipine Nitroso Impurity, with the chemical name 5 - ethyl 7 - methyl 6 - (2 - chlorophenyl) - 8 - methyl - 4 - nitroso - 3,4 - dihydro - 2H - benzo[b][1,4]oxazine - 5,7 - dicarboxylate, may be generated during the synthesis, storage, or degradation of amlodipine. As a potential genotoxic impurity, it has attracted much attention because genotoxic impurities may pose a risk to human health, even at very low concentrations.


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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