Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
In addition to treating various diseases, isotopes are used for imaging, diagnosis, and newborn screening.
Small molecule compounds labeled with stable isotopes can be used as chemical reference for chemical identification, qualitative, quantitative, detection, etc. Various types of NMR solvents can be used to study the structure, reaction mechanism and reaction kinetics of compounds.
Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
General Information |
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Catalog: BLP-008273 |
CAS: 202480-67-9 |
Molecular Formula: C8H3D3Cl2O3 |
Molecular Weight: 224.05 |
Chemical Structure |
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Description | 2,4-Dichlorophenoxyacetic acid-[d3] is the labelled analogue of 2,4-Dichlorophenoxyacetic acid, which is a synthetic auxin, a class of plant growth regulator and herbicide. |
Synonyms | 2,4-dichlorophenoxyacetic acid (ring-d3); (2,4-Dichlorophenoxy-d3)acetic Acid; 2-(2,4-Dichlorophenoxy)acetic Acid-d3; Diclordon-d3; Dicopur-d3; Esterone-d3; Fernimine-d3; Foredex 75-d3; Trinoxol-d3 |
IUPAC Name | 2-(2,4-dichloro-3,5,6-trideuteriophenoxy)acetic acid |
Related CAS | 94-75-7 (unlabelled) |
Canonical SMILES | C1=CC(=C(C=C1Cl)Cl)OCC(=O)O |
InChI | InChI=1S/C8H6Cl2O3/c9-5-1-2-7(6(10)3-5)13-4-8(11)12/h1-3H,4H2,(H,11,12)/i1D,2D,3D |
InChI Key | OVSKIKFHRZPJSS-CBYSEHNBSA-N |
Melting Point | 137-139°C |
Purity | 96%; ≥98% atom D |
Solubility | Slightly soluble in DMSO, Methanol |
Appearance | White to Off-white Solid |
Storage | Store at 2-8°C |
2,4-Dichlorophenoxyacetic acid-[d3], a deuterated variant of the synthetic auxin herbicide 24-D, acts as a versatile analytical tool in diverse scientific research domains. Here are key applications crafted with high perplexity and burstiness:
Environmental Monitoring: Serving as an internal standard in environmental assessments, 2,4-Dichlorophenoxyacetic acid-[d3] aids in quantifying the presence of non-deuterated 24-D in soil and water samples. This pivotal role enables researchers to gauge contamination levels and assess the efficacy of remediation tactics. Accurate quantification facilitates the generation of reliable data on pesticide distribution and environmental repercussions.
Metabolic Studies: Within plant biochemistry, 2,4-Dichlorophenoxyacetic acid-[d3] plays a crucial role in delving into the metabolic pathways and degradation patterns of 24-D in plants. By tracking the assimilation and transformation of the labeled compound, scientists glean insights into detoxification mechanisms and metabolite genesis. This knowledge is paramount for unraveling herbicide metabolism intricacies and selecting resilient plant cultivars.
Residue Analysis: Widely utilized in agricultural investigations, the compound aids in scrutinizing pesticide residues in crops. Leveraging the deuterated form as an assessment benchmark, laboratories can meticulously detect trace quantities of 24-D in food commodities. This meticulous approach ensures adherence to safety protocols and facilitates the advancement of secure agricultural methodologies.
Pharmaceutical Research: In the realm of drug delivery exploration, 2,4-Dichlorophenoxyacetic acid-[d3] emerges as a pivotal tool for investigating drug-molecule interactions through isotopic labeling. Researchers harness this compound to probe the binding dynamics and impact of small molecules on proteins or other biomolecules. This application lays the groundwork for a comprehensive comprehension of drug functionality and the evolution of precision-targeted therapeutics.
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