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-008677 |
CAS: 2483824-12-8 |
Molecular Formula: [13C]3HD9ClN |
Molecular Weight: 107.61 |
Chemical Structure |
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Description | Trimethylamine-[13C3,D9] hydrochloride is a labelled form of Trimethylamine hydrochloride. Trimethylamine hydrochloride is a precursor to prepare aluminium chloride-trimethylamine hydrochloride ionic liquid, which is commonly used in electrodeposition of aluminum wires. |
Related CAS | 593-81-7 (unlabelled) |
Purity | 98% |
Trimethylamine-[13C3,D9] hydrochloride, a stable isotopically labeled compound, finds utility across diverse scientific research domains. Here are key applications of Trimethylamine-[13C3,D9] hydrochloride presented with high perplexity and burstiness:
Metabolic Tracing: Facilitating metabolic investigations, this compound acts as a tracer in metabolic studies to unravel the intricate pathways governing trimethylamine metabolism in biological systems. Through the substitution of standard trimethylamine with an isotopically labeled variant, researchers can meticulously monitor the metabolic destiny and transformation of molecules, shedding light on metabolic pathways and disorders linked to trimethylamine metabolism.
Mass Spectrometry Analysis: In the realm of analytical chemistry, Trimethylamine-[13C3,D9] hydrochloride assumes the role of an internal standard for mass spectrometry (MS) assays. This compound stands as a precise reference point, ensuring the exactness and consistency of quantitative analyses. This technique holds paramount importance in disciplines such as pharmacokinetics, environmental monitoring, and diverse biochemical studies.
NMR Spectroscopy Studies: Leveraging its stable isotopic labeling, Trimethylamine-[13C3,D9] hydrochloride serves as a valuable asset in nuclear magnetic resonance (NMR) spectroscopy for exploring molecular structures and dynamics. The inclusion of the labeled compound amplifies the resolution and sensitivity of NMR signals, facilitating in-depth examinations of chemical environments. This application plays a pivotal role in domains like structural biology, organic chemistry, and the arena of drug discovery.
Biochemical Research: Within the realm of bioscience research, Trimethylamine-[13C3,D9] hydrochloride is integrated into biochemical assays to scrutinize reactions associated with methylation processes and nitrogen metabolism. By harnessing the potential of the labeled compound, scientists can glean insights into enzyme functionalities and mechanisms of reactions. These investigations contribute significantly to the comprehension of cellular metabolism and the advancement of therapeutic strategies.
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