
N-Nitroso Bevantolol NEW
Price | Get Latest Price | ||
Package | 5mg | 20mg | 50mg |
Min. Order: | 1mg |
Supply Ability: | 10000 |
Update Time: | 2025-07-31 |
Product Details
Product Name: N-Nitroso Bevantolol | Min. Order: 1mg |
Purity: >95% HPLC | Supply Ability: 10000 |
Release date: 2025/07/31 | |
Molecular Formula:: C20H26N2O5 | Molecular Weight:: 374.43 |
Appearance: Almost White soild | Storage: 2-8°C Refrigerator |
Product Catalog: | B081002 |
CAS No.: | |
Product Name: | N-Nitroso Bevantolol |
Purity: | >95% HPLC |
Synonyms: | N-(3,4-dimethoxyphenethyl)-N-(2-hydroxy-3-(m-tolyloxy)propyl)nitrous amide |
Molecular Formula: | C20H26N2O5 |
Mol. Weight: | 374.43 |
Appearance: | Almost White 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: | N - Nitroso Bevantolol is a nitrosamine impurity that may be present in bevanolol drugs. Bevantolol is a fourth - generation beta - blocker used to treat cardiovascular diseases such as hypertension and angina pectoris. The impurity may be formed during the production process of bevanolol due to improper reaction conditions or the presence of certain components in the raw materials. In addition, factors such as inappropriate storage conditions of the drug may also contribute to the generation of N - Nitroso Bevantolol. |
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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