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-010705 |
CAS: 122025-09-6 |
Molecular Formula: C8H8D3N |
Molecular Weight: 124.20 |
Chemical Structure |
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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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