• 1. Enabling shape memory and healable effects in a conjugated polymer by incorporating siloxane via dynamic imine bond?
  Yaling Zhang,Chunhui Dai,Shiwei Zhou,Bin Liu Chem. Commun., 2018,54, 10092-10095
• 2. Evolution of shape, size, and areal density of a single plane of Si nanocrystals embedded in SiO2 matrix studied by atom probe tomography
  Bin Han,Yasuo Shimizu,Gabriele Seguini,Celia Castro,Gérard Ben Assayag,Koji Inoue,Yasuyoshi Nagai,Sylvie Schamm-Chardon,Michele Perego RSC Adv., 2016,6, 3617-3622
• 3. Fc microparticles can modulate the physical extent and magnitude of complement activity?
  David White,Sean R. Stowell Biomater. Sci., 2017,5, 463-474
• 4. Dissolved oxygen sensor based on fluorescence quenching of oxygen-sensitive ruthenium complexes immobilized in sol–gel-derived porous silica coatings
  Analyst, 1996,121, 785-788
• 5. Empowering microfluidics by micro-3D printing and solution-based mineral coating?
  Hongxia Li,Aikifa Raza,Qiaoyu Ge,Jin-You Lu,TieJun Zhang Soft Matter, 2020,16, 6841-6849

• Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Fatty Acyls Fatty acids and conjugates Long-chain fatty acids
• Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Fatty Acyls Long-chain fatty acids

Exploring the Unique Properties and Applications of 16-Heptadecynoic acid,12-hydroxy-, (S)- (9CI) (CAS No. 148019-74-3)

16-Heptadecynoic acid,12-hydroxy-, (S)- (9CI) (CAS No. 148019-74-3) is a specialized fatty acid derivative that has garnered significant attention in biochemical and pharmaceutical research. This compound, characterized by its hydroxy and alkynyl functional groups, exhibits unique structural features that make it valuable for various applications. Researchers are particularly interested in its potential role in lipid metabolism, anti-inflammatory pathways, and bioactive molecule synthesis.

The (S)-enantiomer configuration of this compound is crucial for its biological activity, as it often determines how the molecule interacts with enzymes and receptors. This specificity is why 16-Heptadecynoic acid,12-hydroxy-, (S)- (9CI) is frequently studied in the context of chiral chemistry and stereoselective synthesis. Its hydroxy group at the 12th carbon position further enhances its reactivity, making it a versatile intermediate in organic synthesis.

Recent studies have explored the potential of 16-Heptadecynoic acid,12-hydroxy-, (S)- (9CI) in nutraceutical and cosmeceutical applications. With growing consumer interest in natural bioactive compounds, this molecule’s ability to influence skin hydration and cellular repair mechanisms has positioned it as a candidate for advanced skincare formulations. Additionally, its role in modulating lipid signaling pathways aligns with current trends in personalized nutrition and functional foods.

From a synthetic chemistry perspective, 16-Heptadecynoic acid,12-hydroxy-, (S)- (9CI) serves as a building block for more complex molecules. Its alkyne moiety allows for click chemistry applications, a rapidly growing field in drug discovery and material science. Researchers are also investigating its use in bioconjugation techniques, which are essential for developing targeted therapies and diagnostic tools.

The market for specialized fatty acids like 16-Heptadecynoic acid,12-hydroxy-, (S)- (9CI) is expanding, driven by demand in pharmaceutical intermediates and high-value biochemicals. As industries seek sustainable and efficient production methods, innovations in enzymatic synthesis and green chemistry are likely to play a pivotal role in scaling up its availability. This compound’s unique properties ensure its relevance in both academic research and industrial applications.

In summary, 16-Heptadecynoic acid,12-hydroxy-, (S)- (9CI) (CAS No. 148019-74-3) is a multifaceted molecule with promising applications across biomedical research, cosmetics, and organic synthesis. Its structural features and biological activity make it a subject of ongoing investigation, particularly in areas aligned with modern scientific and consumer trends. As research progresses, its potential to contribute to advancements in health and wellness and sustainable chemistry will continue to grow.

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