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1,1,2-Trichloroethane-1,2,2-[d3]

General Information
Catalog: BLP-008257
CAS: 171086-93-4
Molecular Formula: C2D3Cl3
Molecular Weight: 136.42
Chemical Structure
1,1,2-Trichloroethane-1,2,2-[d3]
Synonyms Trichloroethane-D3; Vinyltrichloride-d3; 1,1,2-trichloroethane (1,2,2-D3)
IUPAC Name 1,1,2-trichloro-1,2,2-trideuterioethane
Related CAS 79-00-5 (unlabelled)
Isomeric SMILES [2H]C([2H])(C([2H])(Cl)Cl)Cl
Canonical SMILES C(C(Cl)Cl)Cl
InChI InChI=1S/C2H3Cl3/c3-1-2(4)5/h2H,1H2/i1D2,2D
InChI Key UBOXGVDOUJQMTN-FUDHJZNOSA-N
Purity 98%; 98% atom D
Solubility Sparingly soluble in Chloroform; Slightly soluble in Methanol
Appearance Colorless Oily Matter
Storage Store at 2-8°C under inert atmosphere

1,1,2-Trichloroethane-1,2,2-[d3], a deuterated chemical compound with diverse scientific and industrial applications, serves as a pivotal tool in multiple fields. Here are key applications of 1,1,2-Trichloroethane-1,2,2-[d3] presented with high perplexity and burstiness:

Analytical Chemistry: A cornerstone in gas chromatography-mass spectrometry (GC-MS) analyses, this compound acts as an internal standard, with its stable isotopic composition enabling precise quantification of its non-deuterated counterpart in environmental and biological samples. By comparing the responses of the deuterated and non-deuterated versions, chemists achieve meticulous measurements of trace contaminants with unparalleled accuracy.

Environmental Monitoring: Embracing 1,1,2-Trichloroethane-1,2,2-[d3] in environmental studies is paramount for tracking the fate and transport of VOCs in ecosystems. Researchers leverage its properties to unravel the degradation and dispersion patterns of these compounds across various mediums like water, air, and soil. This knowledge is indispensable for formulating effective remediation strategies and evaluating environmental repercussions with meticulous detail.

Chemical Research: Within the realm of synthetic chemistry, the deuterated variant of 112-Trichloroethane emerges as a critical asset for exploring reaction mechanisms and kinetic isotope effects. By swapping hydrogen atoms with deuterium, researchers delve into the impact of atomic mass on reaction kinetics and pathways, shedding light on the intricacies of chemical transformations. These revelations drive the development of streamlined and selective chemical processes.

NMR Spectroscopy: Deuterated solvents like 1,1,2-Trichloroethane-1,2,2-[d3] play an indispensable role in nuclear magnetic resonance (NMR) spectroscopy by providing a pristine background that does not disrupt the detection of signals from the analyte. This pristine environment enables scientists to generate high-resolution spectra for unraveling complex molecular structures and assessing purity levels with unmatched precision and clarity.

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