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-006321 |
CAS: 1346606-16-3 |
Molecular Formula: C12H10D4FNO3 |
Molecular Weight: 243.27 |
Chemical Structure |
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Synonyms | 2-(4-Fluorophenoxy-d4)-N-methoxy-N-methyl-1-butene |
IUPAC Name | (E)-4-[methoxy(methyl)amino]-1-(2,3,5,6-tetradeuterio-4-fluorophenoxy)but-3-en-2-one |
Canonical SMILES | CN(C=CC(=O)COC1=CC=C(C=C1)F)OC |
InChI | InChI=1S/C12H14FNO3/c1-14(16-2)8-7-11(15)9-17-12-5-3-10(13)4-6-12/h3-8H,9H2,1-2H3/b8-7+/i3D,4D,5D,6D |
InChI Key | LLUFOXYJKAAINV-PYTYSWDNSA-N |
Solubility | Soluble in Dichloromethane, Chloroform |
Appearance | Red Oily Matter |
Storage | Store at 2-8°C |
2-(4-Fluorophenoxy)-N-methoxy-N-methyl-1-butene-[d4] is a compound enriched with deuterium, commonly utilized in the realms of research and development. Here are the diverse applications of this compound, showcased with heightened perplexity and burstiness:
Stable Isotope Labeling: Embraced as a stable isotope-labeled internal standard in mass spectrometry for precise quantitative analysis, this compound stands out in its deuterium-laden glory. By elegantly substituting strategic hydrogen atoms with deuterium, researchers can unravel the mysteries of metabolic pathways or painstakingly quantify analyte concentrations within intricate mixtures, orchestrating a symphony of accuracy and reliability.
Pharmacokinetic Studies: Unveiling its prowess in the realm of drug development, 2-(4-Fluorophenoxy)-N-methoxy-N-methyl-1-butene-[d4] dances with finesse to illuminate the pharmacokinetics of its non-deuterated counterpart. Through the artful manipulation of deuterium atoms, researchers embark on a journey to decipher the absorption, distribution, metabolism, and excretion (ADME) patterns of the drug, painting a vivid portrait of precision and insight, crucial for optimizing dosing regimens and understanding the drug’s behavioral nuances.
Chemical Reaction Tracing: Embarking on a spectacular voyage into the realm of synthetic organic chemistry, this deuterated marvel unravels the intricate dance of chemical reactions with unparalleled grace. By meticulously observing the fate of deuterium atoms, chemists are bestowed with exquisite insights into the enigmatic world of step-by-step transformations and elusive intermediates. These studies not only augment our comprehension of reaction kinetics but also pave the way for the genesis of novel synthetic methodologies, weaving a tapestry of knowledge and innovation.
Environmental Studies: Casting its gaze upon the environmental domain, 2-(4-Fluorophenoxy)-N-methoxy-N-methyl-1-butene-[d4] emerges as a beacon of insight in unraveling the fate and trajectory of chemicals within ecological systems. With its deuterium cloak, researchers delve into the realms of degradation processes, bioaccumulation dynamics, and environmental persistence, painting a vivid portrait of identification and differentiation. This wealth of information serves as a valuable compass for assessing environmental impact and elevating chemical safety standards to newer heights.
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