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-012036 |
CAS: 119391-92-3 |
Molecular Formula: C11HD14NO |
Molecular Weight: 191.33 |
Chemical Structure |
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Synonyms | N-tert-Butyl-D9-phenyl-D5-nitrone |
IUPAC Name | N-[1,1,1,3,3,3-hexadeuterio-2-(trideuteriomethyl)propan-2-yl]-1-(2,3,4,5,6-pentadeuteriophenyl)methanimine oxide |
Related CAS | 3376-24-7 (unlabelled) |
Canonical SMILES | CC(C)(C)[N+](=CC1=CC=CC=C1)[O-] |
InChI | InChI=1S/C11H15NO/c1-11(2,3)12(13)9-10-7-5-4-6-8-10/h4-9H,1-3H3/i1D3,2D3,3D3,4D,5D,6D,7D,8D |
InChI Key | IYSYLWYGCWTJSG-UYAILFBOSA-N |
Purity | 98% atom D |
Storage | Store at -20°C |
N-tert-Butyl-phenyl-nitrone-[d14], a stable isotope-labeled compound utilized in scientific research, possesses diverse applications. Here are key applications of N-tert-Butyl-phenyl-nitrone-[d14] presented with elevated perplexity and burstiness:
Free Radical Research: Delving into the realm of free radicals, volatile molecules capable of inducing cellular harm, N-tert-Butyl-phenyl-nitrone-[d14] emerges as a pivotal player. Acting as a spin trap, this compound aids in the detection and characterization of free radical species through electron spin resonance (ESR) spectroscopy. This functionality is fundamental for comprehending oxidative stress dynamics and formulating antioxidant strategies.
Pharmacokinetic Studies: The isotope-labeled composition of N-tert-Butyl-phenyl-nitrone-[d14] lends itself seamlessly to the realm of pharmacokinetics. Researchers harness its stable nature to meticulously monitor the compound's absorption, distribution, metabolism, and excretion within the biological system with unparalleled precision. This data proves instrumental in drug development, dosage determination, and adverse effect mitigation, bolstering pharmaceutical endeavors.
Neuroprotection Research: Within the domain of neuroscience, the exploration of N-tert-Butyl-phenyl-nitrone-[d14] uncovers its potential as a neuroprotective agent. Studies delve into its capacity to ameliorate oxidative stress in neuronal cells, shedding light on therapeutic avenues for neurodegenerative afflictions like Alzheimer's and Parkinson's diseases. Unraveling the protective mechanisms of this compound may herald breakthroughs in neurodegeneration management, paving the way for transformative interventions.
Material Science: Extending its reach into material science, N-tert-Butyl-phenyl-nitrone-[d14] plays a pivotal role in the research and development of polymers and advanced materials. Serving as a spin trap, scientists leverage its properties to investigate the stability and degradation processes of polymeric materials under diverse conditions. This knowledge is indispensable for fortifying material resilience and optimizing performance in industrial settings, fostering innovation and durability in material engineering.
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