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Postion:Product Catalog >N-Nitrososarcosine Methyl Ester
N-Nitrososarcosine Methyl Ester
  • N-Nitrososarcosine Methyl Ester
  • N-Nitrososarcosine Methyl Ester
  • N-Nitrososarcosine Methyl Ester
  • N-Nitrososarcosine Methyl Ester
  • N-Nitrososarcosine Methyl Ester

N-Nitrososarcosine Methyl Ester NEW

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Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-07-31

Product Details

Product Name: N-Nitrososarcosine Methyl Ester CAS No.: 51938-19-3
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/07/31

N-Nitrososarcosine Methyl Ester

Article illustration


Product Information

  • Product Code:L030047

  • English Name:N-Nitrososarcosine Methyl Ester

  • English Alias:methyl 2-(methyl(nitroso)amino)acetate

  • CAS No.:51938-19-3

  • Molecular Formula:C?H?N?O?

  • Molecular Weight:132.12

Advantages

  • High-Purity Reference Standard:Confirmed by HPLC (≥99.0%), NMR (1H, 13C), and HRMS, suitable for precise analysis of N-nitroso impurities.

  • Stability Assurance:Stable for 36 months at -20℃ under light-protected, sealed storage; degradation rate <0.1% in methanol-water solution within 6 months.

Applications

  • Quality Control Testing:Used for UPLC-MS/MS detection of N-nitroso impurities in food, pharmaceuticals, and cosmetics, controlling content to meet international regulatory standards (e.g., ≤10 μg/kg in food).

  • Environmental Monitoring:Detects N-Nitrososarcosine Methyl Ester in drinking water, soil, and industrial wastewater via solid-phase extraction coupled with GC-MS, achieving an LOD of 0.1 ng/L.

  • Process Optimization Research:Monitors N-Nitrososarcosine Methyl Ester formed by nitrosation side reactions during amino acid ester synthesis, reducing generation by >70% by adjusting reaction temperature (e.g., 5-10℃) and avoiding nitrite exposure.

Background Description

N-nitroso compounds (NOCs) are known carcinogens prevalent in the environment, food processing, and chemical products. N-Nitrososarcosine Methyl Ester, as a type of NOC, may form during production of sarcosine ester-containing raw materials through reactions between amino groups and nitrites or spontaneous nitrosation under acidic or high-temperature storage conditions. Its nitrosamide group is genotoxic. With stricter regulations on NOCs by WHO, FDA, studying such impurities is crucial for ensuring food and environmental safety.

Research Status

  • Detection Technology:GC-MS/MS with a DB-5MS column (30m×0.25mm×0.25μm) and selected ion monitoring (SIM) mode achieves separation within 6 minutes, with an LOD of 0.05 ng/L for trace analysis.

  • Formation Mechanism:Formed by reaction of sarcosine methyl ester with sodium nitrite under acidic conditions (pH<4); optimizing reaction pH (neutral) and adding antioxidants (e.g., vitamin C) inhibits its formation.

  • Safety Evaluation:Animal studies show carcinogenicity, with a permitted daily intake (TTC value) determined as 1.5 μg/day. Accelerated stability testing is ongoing to monitor nitrosation rates under different humidity and light conditions.

  • 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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