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Benzhydrol-[d5]

General Information
Catalog: BLP-010695
CAS: 95450-78-5
Molecular Formula: C13H7D5O
Molecular Weight: 189.26
Chemical Structure
Benzhydrol-[d5]
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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