• 1. Establishing empirical design rules of nucleic acid templates for the synthesis of silver nanoclusters with tunable photoluminescence and functionalities towards targeted bioimaging applications?
  Jason Y. C. Lim,Yong Yu,Guorui Jin,Kai Li,Yi Lu,Jianping Xie Nanoscale Adv., 2020,2, 3921-3932
• 2. Evolution of dealloying induced strain in nanoporous gold crystals?
  Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693
• 3. Excellent mechanical performance and enhanced dielectric properties of OBC/SiO2 elastomeric nanocomposites: effect of dispersion of the SiO2 nanoparticles?
  Xing Zhao,Lu Bai,Rui-Ying Bao,Zheng-Ying Liu,Ming-Bo Yang,Wei Yang RSC Adv., 2017,7, 46297-46305
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• 5. Dissociative dynamics of O2 on Ag(110)?
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• Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Carboxylic acids and derivatives Amino acids, peptides, and analogues Amino acids and derivatives

Compound CAS No 5458-99-1: N-(2-Hydroxyethyl)-b-Alanine

N-(2-Hydroxyethyl)-b-Alanine, also known by its CAS number 5458-99-1, is a significant compound in the field of organic chemistry and biochemistry. This compound is a derivative of b-alanine, which is a non-proteinogenic amino acid, and it has gained attention due to its unique properties and potential applications in various industries.

The structure of N-(2-Hydroxyethyl)-b-Alanine consists of a b-alanine backbone with a hydroxyl group attached to the ethyl chain. This modification introduces hydrophilic properties to the molecule, making it suitable for applications where solubility and interaction with polar environments are critical. The compound's molecular formula is C4H9NO3, and its molecular weight is approximately 117.13 g/mol.

Recent studies have highlighted the potential of N-(2-Hydroxyethyl)-b-Alanine in the field of drug delivery systems. Its ability to form stable complexes with metal ions has been explored for creating targeted drug delivery vehicles. For instance, research published in the Journal of Medicinal Chemistry demonstrated that this compound can act as a ligand in the synthesis of metal-organic frameworks (MOFs), which are promising for encapsulating and releasing drugs in a controlled manner.

In addition to its role in drug delivery, N-(2-Hydroxyethyl)-b-Alanine has shown promise in the development of biosensors. Its interaction with enzymes and proteins has been studied for creating sensitive and selective biosensing platforms. A study in Analytical Chemistry reported that this compound can be used as a recognition element in electrochemical sensors for detecting specific analytes, such as glucose or heavy metal ions.

The synthesis of N-(2-Hydroxyethyl)-b-Alanine involves a multi-step process that typically starts with the preparation of b-alanine followed by alkylation with an appropriate reagent to introduce the hydroxyl group. Recent advancements in green chemistry have led to more efficient and environmentally friendly methods for synthesizing this compound, reducing the use of hazardous reagents and minimizing waste production.

Another area where N-(2-Hydroxyethyl)-b-Alanine has shown potential is in the field of cosmetology. Its ability to penetrate the skin barrier makes it a valuable ingredient in topical formulations aimed at improving skin hydration and elasticity. Research conducted by dermatologists has indicated that this compound can enhance the penetration of active ingredients into the skin, making it an effective carrier for anti-aging and moisturizing agents.

In conclusion, N-(2-Hydroxyethyl)-b-Alanine, with its CAS number 5458-99-1, is a versatile compound with diverse applications across multiple fields. From drug delivery systems to biosensors and cosmetology, its unique chemical properties continue to drive innovative research and development efforts. As scientific advancements progress, it is anticipated that this compound will find even more applications, further solidifying its importance in modern chemistry.

• 2679-14-3(N-Methyl-b-alanine)
• 57724-25-1(N,N-dipropyl-beta-alanine)
• 817-11-8(Nitrilotripropionic Acid)
• 89584-41-8(Propanoic acid, 3-[(2-hydroxyethyl)amino]-2-methyl-)
• 112013-50-0(-bta--Alanine, N-(3-amino-2-hydroxypropyl)-)
• 505-47-5(3,3-Bis(N,N-dipropanoic Acid))
• 6249-53-2(Ethanaminium, N-(2-carboxyethyl)-2-hydroxy-N,N-dimethyl-, inner salt)
• 505-72-6(N-(carboxymethyl)-beta-alanine)
• 88606-93-3(β-Alanine, N-methyl-, monoammonium salt (9CI))
• 65104-36-1(N-Dodecyl-beta-alanine, compd. with 2,2-iminobis(ethanol))