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N-Butyrylglycine-[d7]

General Information
Catalog: BLP-009956
Molecular Formula: C6H4D7NO3
Molecular Weight: 152.2
Chemical Structure
N-Butyrylglycine-[d7]
Description N-Butyrylglycine-[d7] is a labelled N-Butyrylglycine. N-Butyrylglycine is an acyl glycine. Acyl glycines are normally minor metabolites of fatty acids.
Synonyms N-n-Butanoylglycine-d7; Butyrylaminoacetic Acid-d7; N-Butyryl-d7-glycine
Related CAS 20208-73-5 (unlabelled)
Purity 95% by HPLC; 98% atom D

N-Butyrylglycine-[d7], a deuterated analog of N-butyrylglycine, finds widespread use as an internal standard in a variety of biochemical applications. Here are the key applications:

Metabolomic Studies: Widely employed in metabolomic research, N-Butyrylglycine-[d7] plays a crucial role in quantifying N-butyrylglycine levels in biological samples. By integrating this deuterated standard, researchers can achieve precise and reliable quantification in mass spectrometry analyses. This is indispensable for investigating metabolic pathways and unraveling the intricacies of disease mechanisms.

Pharmacokinetics: Serving as an indispensable tool in pharmacokinetic studies, N-Butyrylglycine-[d7] enables the tracing of the metabolic fate and biotransformation of drugs and compounds. Through the use of this labeled standard, scientists can monitor the pharmacokinetics of N-butyrylglycine derivatives with enhanced precision. This advancement facilitates a deeper comprehension of drug metabolism and distribution dynamics.

Quality Control in Analytical Chemistry: A critical component of analytical chemistry, N-Butyrylglycine-[d7] is harnessed to uphold the accuracy and consistency of quantitative measurements. Functioning as an internal standard, it aids in rectifying variability in sample preparation and instrument responses. This ensures the generation of high-quality, reproducible data across diverse research and clinical applications.

Stable Isotope Labeling: In the realm of biochemical research, N-Butyrylglycine-[d7] plays a pivotal role in stable isotope labeling, contributing to the study of metabolic flux and protein modifications. The incorporation of deuterium atoms allows for distinct separation in mass spectrometry, simplifying the tracking and investigation of metabolic processes. This capability is essential for unveiling the complexities of biochemical pathways and interactions, pushing the boundaries of our understanding in this field.

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