2,2,3,3-Tetrafluoropropyl acrylate-1-[13C],2,3,3-[d3]

2,2,3,3-Tetrafluoropropyl acrylate-1-[13C],2,3,3-[d3], a specialized fluorinated compound, is widely utilized in scientific research and advanced material applications. Here, presented with a high degree of perplexity and burstiness, are key applications:

Polymer Science: This fluorinated acrylate, a cornerstone in fluoropolymer synthesis, boasts exceptional chemical resistance and surface energy properties. Its incorporation into polymer matrices enhances durability and reduces friction coefficients in coatings, making it an essential component in diverse applications ranging from non-stick coatings to protective films.

NMR Spectroscopy: Leveraging isotopic labeling with 13C and deuterium (d3), this compound shines in nuclear magnetic resonance (NMR) spectroscopy studies. By providing distinct isotopic signatures, researchers can delve into the structures and dynamics of polymers, closely monitoring the behavior of the labeled monomer within complex systems to deepen insights into material characteristics.

Chemical Synthesis: Positioned at the forefront of synthetic chemistry, 2,2,3,3-Tetrafluoropropyl acrylate-1-[13C],2,3,3-[d3] emerges as a core component in crafting novel materials with fluorinating capabilities. The introduction of fluorine atoms confers exceptional thermal stability and solvent resistance, potentially paving the way for the development of high-performance materials tailored for diverse applications.

Environmental Science: In the realm of environmental research, compounds like 2,2,3,3-Tetrafluoropropyl acrylate assume a critical role in analyzing the behaviors and impacts of fluorinated substances. Its labeled isotopic composition allows for precise tracking of distribution and degradation within ecological systems, offering valuable insights into the environmental fate of fluorinated chemicals and aiding in the assessment of ecological risks.