• 1. Distinct correlation between (CN2)x units and pores: a low-cost method for predesigned wide range control of micropore size of porous carbon?
  Xiaotong Feng,Lei Bian,Jie Ma,Lei Zhou,Xiayan Wang,Guangsheng Guo,Qiaosheng Pu Chem. Commun., 2019,55, 3963-3966
• 2. Estimates of hydride ion stability in condensed systems: energy of formation and solvation in aqueous and polar-organic solvents
  Craig A. Kelly,David R. Rosseinsky Phys. Chem. Chem. Phys., 2001,3, 2086-2090
• 3. Evolution of important glucosinolates in three common Brassica vegetables during their processing into vegetable powder and in vitro gastric digestion
  Nan Fu,Naphaporn Chiewchan,Xiao Dong Chen Food Funct., 2020,11, 211-220
• 4. Fate of single walled carbon nanotubes in wetland ecosystems?
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• 5. Fast synthesis of red Li3BaSrLn3(WO4)8:Eu3+ phosphors for white LEDs under near-UV excitation by a microwave-assisted solid state reaction method and photoluminescence studies
  Bo Wei,Zhenyu Liu,Chen Xie,Shu Yang,Wentao Tang,Aiwei Gu,Wing-Tak Wong,Ka-Leung Wong J. Mater. Chem. C, 2015,3, 12322-12327

• Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Organic sulfonic acids and derivatives Organosulfonic acids and derivatives Organosulfonamides

2-amino-N-ethylethane-1-sulfonamide hydrochloride (CAS 1305712-73-5): A Comprehensive Overview

2-amino-N-ethylethane-1-sulfonamide hydrochloride (CAS 1305712-73-5) is a specialized sulfonamide derivative with growing importance in pharmaceutical and chemical research. This compound, characterized by its aminoethyl sulfonamide structure, has attracted attention due to its potential applications in drug development and biochemical studies. The hydrochloride salt form enhances its stability and solubility, making it particularly valuable for laboratory and industrial use.

The molecular structure of 2-amino-N-ethylethane-1-sulfonamide hydrochloride features both sulfonamide and amino functional groups, which contribute to its unique chemical properties. Researchers are particularly interested in how these functional groups interact with biological systems, as evidenced by increasing searches for "sulfonamide derivatives in drug discovery" and "aminoethyl compounds in medicinal chemistry". The compound's molecular weight of 184.66 g/mol and its water-soluble nature make it suitable for various experimental conditions.

Recent studies have explored the potential of CAS 1305712-73-5 in developing novel therapeutic agents, particularly in areas addressing current health challenges. The scientific community has shown growing interest in how sulfonamide-based compounds might contribute to solutions for antimicrobial resistance, a global health concern. This aligns with trending search queries like "new sulfonamide antimicrobial agents" and "sulfonamide derivatives for infection treatment".

The synthesis of 2-amino-N-ethylethane-1-sulfonamide hydrochloride typically involves the reaction of 2-aminoethanesulfonyl chloride with ethylamine, followed by hydrochloride salt formation. This process has been optimized to achieve high yields and purity, meeting the stringent requirements of pharmaceutical applications. Quality control measures for this compound often include HPLC analysis and spectroscopic characterization, topics frequently searched by analytical chemists ("HPLC analysis of sulfonamide derivatives").

In pharmaceutical formulation, the hydrochloride salt form of this compound offers advantages in terms of bioavailability and stability. Formulation scientists searching for "sulfonamide salt forms in drug development" will find this aspect particularly relevant. The compound's physicochemical properties, including its pKa and partition coefficient, make it an interesting candidate for drug delivery system development.

Beyond pharmaceutical applications, 2-amino-N-ethylethane-1-sulfonamide hydrochloride has shown promise in material science. Researchers investigating "functionalized sulfonamides for material applications" have explored its potential as a building block for advanced polymers and coatings. The compound's ability to form hydrogen bonds and its thermal stability contribute to these emerging applications.

The safety profile of CAS 1305712-73-5 has been studied in accordance with standard laboratory protocols. While not classified as hazardous under normal handling conditions, proper laboratory practices should always be followed. This information addresses common search queries like "safety data for sulfonamide derivatives" and "handling aminoethyl compounds in the lab".

Market analysis indicates growing demand for specialized sulfonamide derivatives like 2-amino-N-ethylethane-1-sulfonamide hydrochloride, particularly in the pharmaceutical and biotechnology sectors. Industry professionals searching for "sulfonamide market trends 2024" will note the compound's increasing importance in drug discovery pipelines and specialty chemical applications.

Storage recommendations for 2-amino-N-ethylethane-1-sulfonamide hydrochloride typically suggest keeping the compound in a cool, dry environment, protected from light and moisture. These handling guidelines respond to frequent searches about "proper storage of sulfonamide compounds" and "stability of aminoethyl derivatives". When stored correctly, the compound maintains its stability for extended periods.

Future research directions for CAS 1305712-73-5 may include exploration of its potential in targeted drug delivery systems and as a scaffold for combinatorial chemistry. These prospects align with current scientific interests reflected in search trends like "sulfonamides in precision medicine" and "multifunctional amine compounds in drug design". The compound's versatility suggests it will remain relevant in various research fields.

For researchers considering working with 2-amino-N-ethylethane-1-sulfonamide hydrochloride, it's important to consult recent literature on its applications and properties. The growing body of research addressing queries such as "recent advances in sulfonamide chemistry" and "applications of aminoethyl sulfonamides" provides valuable insights into current developments with this compound.

In conclusion, 2-amino-N-ethylethane-1-sulfonamide hydrochloride (CAS 1305712-73-5) represents an important sulfonamide derivative with diverse applications in pharmaceutical research and material science. Its unique combination of functional groups and favorable physicochemical properties continue to make it a compound of interest for researchers addressing current scientific challenges and developing innovative solutions in chemistry and medicine.

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