• 1. An integrated process of CO2 capture and in situ hydrogenation to formate using a tunable ethoxyl-functionalized amidine and Rh/bisphosphine system?
  Yu-Nong Li,Liang-Nian He,Xian-Dong Lang,Xiao-Fang Liu,Shuai Zhang RSC Adv., 2014,4, 49995-50002
• 2. An amphipathic trans-acting phosphorothioate RNA element delivers an uncharged phosphorodiamidate morpholino sequence in mdx mouse myotubes?
  H. V. Jain,D. Verthelyi,S. L. Beaucage RSC Adv., 2017,7, 42519-42528
• 3. An atomistic mechanism for the degradation of perovskite solar cells by trapped charge?
  Eunhak Lim,Jiyoung Heo,Seong Keun Kim Nanoscale, 2019,11, 11369-11378
• 4. An Aptamer Bio-barCode (ABC) assay using SPR, RNase H, and probes with RNA and gold-nanorods for anti-cancer drug screening
  Chengbin Yang,Hing Lun Tsang,Pui Man Lau,Ken-Tye Yong,Ho Pui Ho,Siu Kai Kong Analyst, 2017,142, 3579-3587
• 5. An artificial photosynthesis system comprising a covalent triazine framework as an electron relay facilitator for photochemical carbon dioxide reduction?
  Siquan Zhang,Shengyao Wang,Liping Guo,Hao Chen,Bien Tan,Shangbin Jin J. Mater. Chem. C, 2020,8, 192-200

• Solvents and Organic Chemicals Organic Compounds Organohalogen compounds Vinyl halides Vinyl chlorides

Trichloroethylene-13C2 (Stabilized with Diisopropylamine)

Trichloroethylene-13C2, also known as 1,1,2-trichloroethene-d4 or TCE-d4, is a stable isotope-labeled compound with the CAS number 93952-00-2. This compound is widely used in various scientific and industrial applications due to its unique properties and the stability provided by the incorporation of diisopropylamine. The addition of diisopropylamine ensures that the compound remains stable under a range of conditions, making it suitable for use in research and production environments.

The Trichloroethylene-13C2 molecule consists of a trichloroethylene backbone with two carbon atoms replaced by their heavier isotopes, carbon-13. This isotopic substitution does not alter the chemical properties of the compound significantly but allows for precise tracking and analysis in various analytical techniques such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy. The use of stabilized Trichloroethylene-13C2 has become a cornerstone in fields like environmental science, pharmacology, and materials science.

Recent advancements in analytical chemistry have further highlighted the importance of Trichloroethylene-13C2 in studying reaction mechanisms and molecular interactions. For instance, researchers have utilized this compound to investigate the kinetics of organic reactions under controlled conditions. The ability to track the movement and transformation of molecules labeled with 13C isotopes has provided unprecedented insights into complex chemical processes.

In environmental science, Trichloroethylene-13C2 has been instrumental in assessing the fate and transport of contaminants in soil and groundwater systems. By using this stable isotope-labeled compound, scientists can accurately measure degradation rates and pathways, which are critical for designing effective remediation strategies. The stabilization provided by diisopropylamine ensures that the compound remains intact during these studies, yielding reliable results.

The role of diisopropylamine in stabilizing Trichloroethylene-13C2 cannot be overstated. This amine acts as a stabilizing agent by forming hydrogen bonds with the trichloroethylene molecule, preventing decomposition and ensuring long-term stability. This stabilization is particularly important in applications where precise control over molecular integrity is essential, such as in pharmaceutical synthesis or advanced materials research.

Looking ahead, the demand for Trichloroethylene-13C2 (Stabilized with Diisopropylamine) is expected to grow as researchers continue to explore its potential in emerging fields like nanotechnology and green chemistry. Its versatility and reliability make it an invaluable tool for scientists seeking to push the boundaries of chemical research.

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