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

N-Nitroso Sertraline NEW

Price Get Latest Price
Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-06-18

Product Details

Product Name: N-Nitroso Sertraline CAS No.: 3006789-98-3
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/06/18

N-Nitroso Sertraline;3006789-98-3

Article illustration

  • Product Information

  • Product Code:S027038

  • English Name:N-Nitroso Sertraline

  • English Alias:N-((1S,4S)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydronaphthalen-1-yl)-N-methylnitrous amide

  • CAS No.:3006789-98-3

  • Molecular Formula:C??H??Cl?N?O

  • Molecular Weight:335.23

  • Advantages

  • High-Purity Reference Standard:Confirmed by HPLC (≥99.0%), NMR, and HRMS, suitable for precise analysis of nitrosamine impurities in Sertraline.

  • Stability Assurance:Stable for 24 months at -20℃ under light-protected, sealed storage; degradation rate <0.5% in acetonitrile solution within 3 months.

  • Applications

  • Quality Control Testing:Used for LC-MS/MS detection of N-nitroso impurities in Sertraline API and formulations, controlling impurity content to meet ICH M7 standards (≤0.1 ppm).

  • Process Optimization Research:Monitors N-Nitroso Sertraline generated from nitrosation side reactions during Sertraline synthesis, reducing formation by adjusting reaction temperature (e.g., 0-5℃) and pH (weak acidic conditions).

  • Method Validation:Serves as a standard for developing nitrosamine detection methods, verifying UPLC resolution (≥2.0) and LOD (0.005 ng/mL).

  • Background Description

  • Sertraline, a selective serotonin reuptake inhibitor (SSRI), is used in the treatment of depression and other mental illnesses. Nitrosamine impurities (such as N-Nitroso Sertraline) pose potential genotoxic and carcinogenic risks, possibly formed by reactions between secondary amines and nitrosating agents during drug synthesis. With stricter control requirements from international regulatory agencies (FDA, EMA), studying such impurities has become crucial for ensuring Sertraline safety.
  • Research Status

  • Detection Technology:UPLC-MS/MS with C18 column (1.7μm) and 0.1% formic acid-acetonitrile gradient elution achieves separation within 2 minutes, with LOD of 0.003 ng/mL for trace analysis.

  • Formation Mechanism:Originates from nitrosation of the amine group in Sertraline, with higher reactivity under acidic conditions (pH 2-3). Adding nitrosamine inhibitors (e.g., vitamin C) or optimizing purification (e.g., column chromatography) reduces content by >70%.

  • Safety Evaluation:Preliminary toxicology shows positive Ames test results, indicating potential mutagenicity. Current standards limit it to ≤0.1 ppm, requiring continuous monitoring via accelerated and long-term stability studies.

  • 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!

    WhatsAPP: +86 17320513646
    E-mail: anna@molcoo.com


    NEW IN STOCK!

    The Molcoo Laboratory added drug impurity reference standards, including Baricitinib, Piperazine, Benzylpenicillin, Tranilast and multiple N-Nitroso drug impurities! Now available for immediate delivery! 

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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