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4-Chlorodiphenyl Ether-[d5]

General Information
Catalog: BLP-010936
CAS: 93951-85-0
Molecular Formula: C12H4D5ClO
Molecular Weight: 209.68
Chemical Structure
4-Chlorodiphenyl Ether-[d5]
Description 4-Chlorodiphenyl Ether-[d5] is the labelled analogue of 4-Chlorodiphenyl Ether.
Synonyms 4-(Chlorophenyl)phenyl-d5 ether
IUPAC Name 1-(4-chlorophenoxy)-2,3,4,5,6-pentadeuteriobenzene
Related CAS 7005-72-3 (unlabelled)
Canonical SMILES C1=CC=C(C=C1)OC2=CC=C(C=C2)Cl
InChI InChI=1S/C12H9ClO/c13-10-6-8-12(9-7-10)14-11-4-2-1-3-5-11/h1-9H/i1D,2D,3D,4D,5D
InChI Key PGPNJCAMHOJTEF-RALIUCGRSA-N
Boiling Point 161-162°C at 19 mmHg (lit.)
Purity 98% atom D
Density 1.222 g/cm3 at 25°C
Storage Store at RT

4-Chlorodiphenyl Ether-[d5], a deuterium-labeled compound, finds diverse applications in scientific and analytical realms. Here are key applications presented with high perplexity and burstiness:

Analytical Chemistry: A cornerstone of analytical chemistry, 4-Chlorodiphenyl Ether-[d5] acts as an internal standard in mass spectrometry and gas chromatography-mass spectrometry (GC-MS). Its stable isotopic labeling enables precise quantification of chlorinated biphenyl ethers in intricate samples. This facilitates the monitoring of environmental pollutants and ensures adherence to regulatory standards, safeguarding environmental health.

Environmental Studies: Vital for investigating the environmental destiny and migration of chlorinated biphenyl ethers, this compound aids in tracing the degradation and dispersion of these chemicals in diverse ecosystems. By integrating 4-Chlorodiphenyl Ether-[d5] in trace-level analysis, researchers gain insights into the long-term ecological ramifications of persistent organic pollutants, shedding light on environmental sustainability.

Toxicology Research: Serving as a pivotal model compound in toxicology studies, 4-Chlorodiphenyl Ether-[d5] illuminates the toxicokinetics and metabolic pathways of chlorinated ethers. Through examining its absorption, distribution, metabolism, and excretion in biological systems, researchers can foresee potential health hazards associated with exposure to similar chemical substances. These findings inform precise risk assessments and enhance safety regulations, safeguarding human well-being.

Chemical Synthesis: Employed as a labeled precursor in the synthesis of deuterium-labeled analogs of chlorinated aromatic compounds, 4-Chlorodiphenyl Ether-[d5] plays a crucial role in various research domains like material science and pharmacology. These analogs provide detailed insights into reaction mechanisms and compound stability, driving advancements in chemical reactivity studies and compound innovation. The utilization of deuterated compounds supports cutting-edge research in exploring the intricacies of chemical reactions and compound refinement.

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