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Postion:Product Catalog >N-Nitroso Desmethyl Levofloxacin
N-Nitroso Desmethyl Levofloxacin
  • N-Nitroso Desmethyl Levofloxacin
  • N-Nitroso Desmethyl Levofloxacin
  • N-Nitroso Desmethyl Levofloxacin

N-Nitroso Desmethyl Levofloxacin NEW

Price Get Latest Price
Package 5mg 20mg 50mg
Min. Order: 1mg
Supply Ability: 100000
Update Time: 2025-05-27

Product Details

Product Name: N-Nitroso Desmethyl Levofloxacin CAS No.: 1152314-62-9
Min. Order: 1mg Purity: >95% HPLC
Supply Ability: 100000 Release date: 2025/05/27
Molecular Formula:: C17H17FN4O5 Molecular Weight:: 376.34
Appearance: White soild Storage: 2-8°C Refrigerator


Product Catalog:L004028
CAS No.:1152314-62-9
Product Name:N-Nitroso Desmethyl Levofloxacin
Purity:>95% HPLC
Synonyms: (S)-9-fluoro-3-methyl-10-(4-nitrosopiperazin-1-yl)-7-oxo-2,3-dihydro-7H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid
Molecular Formula:C17H17FN4O5
Mol. Weight:376.34
Appearance: 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 Desmethyl Levofloxacin is recognized as an impurity of levofloxacin, a commonly prescribed antibacterial agent. Investigating such impurities is crucial as it directly impacts the quality and safety profile of pharmaceutical products. In the realm of pharmaceutical research, this compound serves as a key element in new drug development endeavors. It enables scientists to trace the degradation pathways and transformation mechanisms of levofloxacin, thereby facilitating the refinement of synthesis methods and the establishment of more stringent quality control measures to guarantee the efficacy and reliability of levofloxacin - based medications.


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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