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-010695 |
CAS: 95450-78-5 |
Molecular Formula: C13H7D5O |
Molecular Weight: 189.26 |
Chemical Structure |
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Description | Benzhydrol-[d5] is the labelled analogue of Benzhydrol, which is an intermediate in the preparation of Modafinil. |
Synonyms | Benzhydrol D5; Benzene-d5-methanol, a-phenyl-; α-Phenylbenzenemethanol-d5; Benzhydryl Alcohol-d5; Benzohydrol-d5; Diphenylcarbinol-d5; Diphenylmethanol-d5; Diphenylmethyl Alcohol-d5; Hydroxydiphenylmethane-d5; NSC 32150-d5; α-Phenylbenzyl Alcohol-d5 |
IUPAC Name | (2,3,4,5,6-pentadeuteriophenyl)-phenylmethanol |
Related CAS | 91-01-0 (unlabelled) |
Isomeric SMILES | [2H]C1=C(C(=C(C(=C1[2H])[2H])C(C2=CC=CC=C2)O)[2H])[2H] |
Canonical SMILES | C1=CC=C(C=C1)C(C2=CC=CC=C2)O |
InChI | InChI=1S/C13H12O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13-14H/i1D,3D,4D,7D,8D |
InChI Key | QILSFLSDHQAZET-DYVTXVBDSA-N |
Melting Point | 66-69°C |
Purity | ≥98%; ≥98% atom D |
Solubility | Slightly soluble in Acetonitrile, Chloroform |
Appearance | White to Off-white Solid |
Storage | Store at RT under inert atmosphere |
Benzhydrol-[d5], a deuterated chemical compound widely embraced in scientific realms, finds diverse applications. Here are key uses of Benzhydrol-[d5] presented with a high degree of perplexity and burstiness:
Stable Isotope Labeling: In the domain of mass spectrometry, Benzhydrol-[d5] plays a pivotal role as a stable isotope-labeled entity. By integrating deuterium into biological molecules, researchers can meticulously track and dissect compounds within intricate mixtures with exceptional precision. This aids in quantifying metabolic pathways, unraveling pharmacokinetics, and scrutinizing drug metabolism dynamics with acute accuracy.
Synthetic Chemistry: Within the realm of organic synthesis, Benzhydrol-[d5] emerges as a critical building block for crafting deuterated compounds. These deuterated analogs are paramount for probing reaction mechanisms and refining the selectivity of specific catalysts. Furthermore, the utilization of Benzhydrol-[d5] enhances NMR analysis, as the deuterium atoms diminish background noise, presenting crystal-clear spectral insights.
Pharmaceutical Research: Delving into drug development, Benzhydrol-[d5] stands as a linchpin in crafting deuterium-labeled drugs that boast enhanced stability and prolonged half-life, augmenting therapeutic efficacy. Pharmaceutical enterprises leverage this compound to delve into the pharmacodynamics and pharmacokinetics of novel drugs, fostering comprehension for optimized dosages and bolstering therapeutic outcomes.
Environmental Studies: Within the realm of environmental research, Benzhydrol-[d5] serves as an invaluable tracer to examine the dispersal and movement of chemicals within ecosystems. By monitoring the dispersion of this compound, scientists glean profound insights into the behaviors of pollutants and their potential ecological repercussions. This application aids in evaluating environmental hazards and fostering strategies for mitigating pollution impacts.
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