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-010623 |
CAS: 126839-95-0 |
Molecular Formula: C11H11D5O |
Molecular Weight: 169.28 |
Chemical Structure |
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Synonyms | 4-n-Pentylphenol-2,3,5,6-d4,OD; 4-Amylphenol-2,3,5,6-d4,OD; 4-n-Amylphenol-2,3,5,6-d4,OD; 4-n-Pentylphenol-2,3,5,6-d4,OD; Amyl p-Hydroxybenzene-2,3,5,6-d4,OD; p-Amylphenol-2,3,5,6-d4,OD; p-Hydroxy-n-Pentylbenzene-2,3,5,6-d4,OD; p-Pentylphenol-2,3,5,6-d4,OD |
IUPAC Name | 1,2,4,5-tetradeuterio-3-deuteriooxy-6-pentylbenzene |
Related CAS | 14938-35-3 (unlabelled) |
Canonical SMILES | CCCCCC1=CC=C(C=C1)O |
InChI | InChI=1S/C11H16O/c1-2-3-4-5-10-6-8-11(12)9-7-10/h6-9,12H,2-5H2,1H3/i6D,7D,8D,9D/hD |
InChI Key | ZNPSUQQXTRRSBM-WLWDFMJJSA-N |
Purity | 98% atom D |
Solubility | Soluble in Water |
Appearance | Liquid |
Storage | Store at 2-8°C |
4-n-Pentylphenol-[d5], a deuterated chemical compound, is a versatile tool in scientific research for investigating various biochemical and environmental processes. Here are key applications presented with high perplexity and burstiness:
Environmental Fate Studies: In the realm of environmental science, 4-n-Pentylphenol-[d5] plays a pivotal role in illuminating the behavior and destiny of alkylphenols within ecosystems. Researchers leverage this isotopically labeled compound to meticulously track the degradation, distribution, and accumulation of alkylphenols in both aquatic and terrestrial systems. This data serves as a cornerstone for evaluating environmental risks and shaping regulatory frameworks safeguarding our natural world.
Metabolic Pathway Elucidation: Within the domain of biochemical research, 4-n-Pentylphenol-[d5] emerges as a critical instrument for unraveling the intricate metabolic pathways within organisms. The deuterated label provides scientists with a potent tool to trace the processing and transformation of the compound in biological systems, employing cutting-edge techniques like mass spectrometry. By delving into metabolic intermediates and final products, researchers gain profound insights into pentylphenol metabolism, shedding light on potential toxicological implications and advancing our comprehension of biological processes.
Chemical Reaction Mechanisms: Delving into the realm of chemical kinetics, 4-n-Pentylphenol-[d5] proves invaluable for investigating reaction mechanisms involving phenolic compounds. Through the utilization of this deuterated variant, chemists embark on a journey to explore reaction pathways and unravel isotope effects in experimental setups. This endeavor aids in delineating reaction kinetics and mechanisms, ultimately fueling the development of more streamlined synthetic strategies, pushing the boundaries of chemical innovation.
Analytical Method Development: In the meticulous realm of analytical chemistry, 4-n-Pentylphenol-[d5] assumes a pivotal role as an internal standard for refining and validating analytical methodologies. Serving as a steadfast reference point, this compound facilitates the calibration and validation of analytical techniques, ensuring precise measurement of concentration levels of phenolic compounds within complex matrices. This application stands as a cornerstone for guaranteeing accuracy and reproducibility in analytical assays, underpinning the robustness of scientific research endeavors.
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