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Benzylmethylamine-[d3]

General Information
Catalog: BLP-010705
CAS: 122025-09-6
Molecular Formula: C8H8D3N
Molecular Weight: 124.20
Chemical Structure
Benzylmethylamine-[d3]
Synonyms Benzylmethyl-d3-amine; Benzenemethanamine, N-(methyl-d3)-; N-Methylbenzylamine-d3; N-Methylbenzenemethanamine-d3; N-Methyl-N-(phenylmethyl)amine-d3; N-Methyl-N-benzylamine-d3; N-Benzylmethylamine-d3; N-Methyl-1-phenylmethanamine-d3; N-(Phenylmethyl)methylamine-d3; N-Benzyl-N-methylamine-d3; NSC 8059-d3
IUPAC Name N-benzyl-1,1,1-trideuteriomethanamine
Related CAS 103-67-3 (unlabelled)
Canonical SMILES CNCC1=CC=CC=C1
InChI InChI=1S/C8H11N/c1-9-7-8-5-3-2-4-6-8/h2-6,9H,7H2,1H3/i1D3
InChI Key RIWRFSMVIUAEBX-FIBGUPNXSA-N
Purity 99% by HPLC; 99% atom D
Solubility Soluble in Chloroform, Methanol
Appearance Clear Colorless Oily Matter
Storage Store at RT

Benzylmethylamine-[d3], a deuterated variant of benzylmethylamine commonly employed as a tracer or internal standard in analytical chemistry, offers a myriad of applications. Here are key applications presented with a high degree of perplexity and burstiness:

Analytical Chemistry: Positioned as an internal standard in mass spectrometry within the realm of analytical chemistry, Benzylmethylamine-[d3] plays a pivotal role in quantitative analysis. Its stable isotopic constitution enables the precise quantification of benzylmethylamine within intricate mixtures, elevating the accuracy and dependability of analytical outcomes, particularly in the realms of pharmacokinetic inquiries and investigations into drug metabolism.

Pharmaceutical Research: Delving into drug development and pharmacological explorations, Benzylmethylamine-[d3] emerges as a labeled compound essential for tracking and comprehending metabolic pathways. Researchers leverage this compound to monitor the transformation of benzylmethylamine-related drugs and pinpoint metabolites—a process critical for refining drug formulations and evaluating metabolic steadiness.

Stable Isotope Labeling: The utilization of Benzylmethylamine-[d3] in stable isotope labeling experiments unveils a window into the migration and dispersion of the parent compound across biological systems. This methodology yields invaluable insights into metabolic velocities and pathways, guiding researchers in decoding biological functionalities and interactions—a fundamental aspect of exploring dynamic processes in systems biology.

Chemical Synthesis: Within the realm of synthetic chemistry, Benzylmethylamine-[d3] finds its niche as a tool for introducing deuterium atoms into organic compounds. Serving as a deuterated reagent, it proves invaluable in mechanistic inquiries and experiments delving into kinetic isotope effects. Harnessing Benzylmethylamine-[d3], chemists can unravel reaction mechanisms and fine-tune synthetic pathways for the production of deuterated pharmaceuticals, marking a significant stride in pharmaceutical chemistry.

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