Cas no 1219804-86-0 (4-Chloroanisole-2,3,5,6-d4)

4-Chloroanisole-2,3,5,6-d4 is a deuterated analog of 4-chloroanisole, where four hydrogen atoms are replaced with deuterium at the 2, 3, 5, and 6 positions of the aromatic ring. This isotopic labeling enhances the compound's utility in mass spectrometry and NMR studies, providing improved signal resolution and reduced interference in analytical applications. Its high isotopic purity and chemical stability make it suitable for use as an internal standard in quantitative analysis, particularly in environmental and pharmaceutical research. The deuterated structure also facilitates mechanistic studies in organic and medicinal chemistry, offering insights into reaction pathways and metabolic processes.
4-Chloroanisole-2,3,5,6-d4 structure
4-Chloroanisole-2,3,5,6-d4 structure
Product Name:4-Chloroanisole-2,3,5,6-d4
CAS No:1219804-86-0
MF:C7H7ClO
MW:142.582881212234
CID:1065847
Update Time:2025-05-24

4-Chloroanisole-2,3,5,6-d4 Chemical and Physical Properties

Names and Identifiers

    • 4-Chloroanisole-2,3,5,6-d4
    • 4-Chloroanisole--d4
    • Inchi: 1S/C7H7ClO/c1-9-7-4-2-6(8)3-5-7/h2-5H,1H3
    • InChI Key: YRGAYAGBVIXNAQ-UHFFFAOYSA-N
    • SMILES: O(C1C([H])=C([H])C(Cl)=C([H])C=1[H])C

4-Chloroanisole-2,3,5,6-d4 Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
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Additional information on 4-Chloroanisole-2,3,5,6-d4

Comprehensive Overview of 4-Chloroanisole-2,3,5,6-d4 (CAS No. 1219804-86-0): Applications and Analytical Insights

The deuterated compound 4-Chloroanisole-2,3,5,6-d4 (CAS No. 1219804-86-0) is a chemically modified derivative of 4-chloroanisole, where four hydrogen atoms are replaced with deuterium isotopes. This isotopic labeling enhances its utility in advanced analytical techniques, particularly in mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy. Researchers and industries increasingly rely on such labeled compounds for precise metabolic studies, environmental tracing, and pharmaceutical development, aligning with the growing demand for high-purity reagents in life sciences.

In the context of current scientific trends, 4-Chloroanisole-2,3,5,6-d4 is pivotal in stable isotope labeling applications. Its deuterium atoms provide distinct spectral signatures, enabling accurate quantification in complex matrices. This property is especially valuable in drug metabolism research, where understanding metabolite pathways is critical for precision medicine and toxicology assessments. Recent publications highlight its role in elucidating the degradation pathways of agrochemicals, addressing global concerns about environmental persistence and sustainable agriculture.

The synthesis of 4-Chloroanisole-2,3,5,6-d4 involves meticulous deuterium incorporation protocols to ensure isotopic purity, a topic frequently searched by chemists exploring isotope effects or reaction mechanisms. Its stability under physiological conditions makes it a preferred internal standard in LC-MS workflows, a technique dominating discussions in analytical chemistry forums and method validation studies. Furthermore, its compatibility with green chemistry principles—minimizing hazardous byproducts—resonates with industries prioritizing eco-friendly synthesis.

Beyond research, CAS No. 1219804-86-0 is gaining attention in flavor and fragrance analysis. Chloroanisole derivatives are known contributors to off-flavors in food and beverages, and the deuterated variant aids in detecting trace contaminants at parts-per-trillion levels. This aligns with consumer-driven demands for food safety and quality control, topics frequently queried in search engines by quality assurance professionals.

From a commercial perspective, the compound’s niche applications in high-value chemical manufacturing and diagnostic reagent formulation underscore its economic significance. Suppliers often highlight its batch-to-batch consistency and regulatory compliance (e.g., REACH, FDA guidelines), addressing procurement concerns raised in B2B marketplaces. As AI-driven drug discovery accelerates, the demand for such specialized reagents is projected to rise, reflecting broader shifts toward data-driven R&D.

In summary, 4-Chloroanisole-2,3,5,6-d4 exemplifies the intersection of isotopic chemistry and modern analytical challenges. Its versatility across pharmaceutical, environmental, and industrial sectors positions it as a critical tool in advancing scientific and commercial objectives, while its technical nuances continue to inspire academic discourse and innovation.

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