• 1. An inter-tangled network of redox-active and conducting polymers as a cathode for ultrafast rechargeable batteries
  Jieun Kim,Han-Saem Park,Tae-Hee Kim,Sung Yeol Kim,Hyun-Kon Song Phys. Chem. Chem. Phys., 2014,16, 5295-5300
• 2. An astrophysically-relevant mechanism for amino acid enantiomer enrichment
  Stephen P. Fletcher,Richard B. C. Jagt,Ben L. Feringa Chem. Commun., 2007, 2578-2580
• 3. Ambient electrochemical NH3 synthesis from N2 and water enabled by ZrO2 nanoparticles?
  Tong Xu,Dongwei Ma,Chengbo Li,Qian Liu,Siyu Lu,Abdullah M. Asiri,Chun Yang,Xuping Sun Chem. Commun., 2020,56, 3673-3676
• 4. An antimonate pyrochlore (H1.23Sr0.45SbO3.48) for photocatalytic oxidation of benzene: effective oxygen usage and excellent activity?
  Jing Chen,Yu Shao,Danzhen Li J. Mater. Chem. A, 2017,5, 937-941
• 5. An AuNPs-functionalized AlGaN/GaN high electron mobility transistor sensor for ultrasensitive detection of TNT?
  Ying Li,Weirong Yao,Yunfei Xie,Renjun Pei RSC Adv., 2015,5, 98724-98729

• Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Carboxylic acids and derivatives Amino acids, peptides, and analogues Amino acids and derivatives

Comprehensive Overview of Asparagine, ethyl ester (CAS No. 7647-24-22-3): Properties, Applications, and Research Insights

Asparagine, ethyl ester (CAS No. 7647-24-22-3) is a derivative of the naturally occurring amino acid asparagine, modified by the introduction of an ethyl ester group. This modification enhances its solubility and stability, making it a valuable compound in biochemical research, pharmaceutical development, and food science. The ethyl ester moiety is particularly significant, as it improves the compound's bioavailability and facilitates its incorporation into peptide synthesis and other enzymatic processes.

In recent years, the demand for specialized amino acid derivatives like Asparagine, ethyl ester has surged, driven by advancements in peptide-based therapeutics and nutraceuticals. Researchers are increasingly exploring its role in drug delivery systems due to its ability to enhance membrane permeability. Additionally, its applications in flavor enhancement and food preservation have garnered attention, aligning with the growing consumer interest in clean-label ingredients and functional foods.

The synthesis of Asparagine, ethyl ester typically involves the esterification of L-asparagine with ethanol under controlled conditions. This process ensures high purity and yield, which are critical for its use in pharmaceutical formulations. Analytical techniques such as HPLC and NMR spectroscopy are routinely employed to verify its structural integrity and purity, addressing the stringent quality standards required in industrial and academic settings.

From a biochemical perspective, Asparagine, ethyl ester serves as a versatile building block in peptide synthesis. Its compatibility with solid-phase peptide synthesis (SPPS) protocols makes it a preferred choice for constructing complex peptides with potential therapeutic benefits. Recent studies have highlighted its utility in designing antioxidant peptides and anti-inflammatory agents, reflecting the broader trend toward personalized medicine and targeted therapies.

Environmental and safety considerations are also paramount when working with Asparagine, ethyl ester. While it is generally regarded as safe for laboratory use, proper handling protocols must be followed to minimize exposure. Its biodegradability and low toxicity profile make it an environmentally friendly option compared to synthetic alternatives, resonating with the global push for sustainable chemistry practices.

In the context of market trends, the compound's niche applications in cosmeceuticals and sports nutrition have sparked commercial interest. For instance, its hydrating properties are being leveraged in skincare formulations, while its role in muscle recovery is under investigation for performance-enhancing supplements. These developments align with the rising consumer demand for science-backed, multifunctional ingredients.

To address common queries from researchers and industry professionals: Asparagine, ethyl ester is not classified as a hazardous material, but its storage recommendations include protection from moisture and extreme temperatures. Frequently asked questions also revolve around its shelf life, solubility in various solvents, and compatibility with other amino acid derivatives—all of which are well-documented in peer-reviewed literature.

In summary, Asparagine, ethyl ester (CAS No. 7647-24-22-3) exemplifies the intersection of organic chemistry and applied biosciences. Its multifaceted applications, from drug development to food technology, underscore its relevance in contemporary research. As scientific inquiry continues to evolve, this compound is poised to play an increasingly pivotal role in addressing challenges across diverse industries.

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