Cas no 1276197-31-9 (N-(3-Methylcrotonyl)glycine-2,2-d2)

N-(3-Methylcrotonyl)glycine-2,2-d2 is a deuterated analog of N-(3-methylcrotonyl)glycine, featuring two deuterium atoms at the 2-position of the glycine moiety. This isotopic labeling enhances its utility in metabolic studies, particularly in tracing biochemical pathways involving leucine catabolism. The incorporation of deuterium allows for precise tracking via mass spectrometry or NMR, improving analytical sensitivity and resolution. Its stable isotopic form minimizes metabolic interference, making it valuable for in vivo and in vitro research. The compound is particularly relevant in investigations of 3-methylcrotonyl-CoA carboxylase deficiency and related metabolic disorders, providing insights into enzyme function and substrate specificity. High chemical purity ensures reliable experimental reproducibility.
N-(3-Methylcrotonyl)glycine-2,2-d2 structure
1276197-31-9 structure
Product Name:N-(3-Methylcrotonyl)glycine-2,2-d2
CAS No:1276197-31-9
MF:C7H11NO3
MW:157.167142152786
CID:1066119
Update Time:2025-10-25

N-(3-Methylcrotonyl)glycine-2,2-d2 Chemical and Physical Properties

Names and Identifiers

    • N-(3-Methylcrotonyl)glycine-2,2-d2
    • 3-METHYLCROTONYLGLYCINE (GLYCINE-2,2-D2, 98%)
    • Inchi: 1S/C7H11NO3/c1-5(2)3-6(9)8-4-7(10)11/h3H,4H2,1-2H3,(H,8,9)(H,10,11)
    • InChI Key: PFWQSHXPNKRLIV-UHFFFAOYSA-N
    • SMILES: C(=O)(C=C(C)C)NC([H])([H])C(=O)O

N-(3-Methylcrotonyl)glycine-2,2-d2 Pricemore >>

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Additional information on N-(3-Methylcrotonyl)glycine-2,2-d2

N-(3-Methylcrotonyl)glycine-2,2-d2 (CAS No. 1276197-31-9): A Comprehensive Guide to Its Properties and Applications

N-(3-Methylcrotonyl)glycine-2,2-d2 (CAS No. 1276197-31-9) is a deuterated derivative of N-(3-Methylcrotonyl)glycine, a compound of significant interest in biochemical and pharmaceutical research. The incorporation of deuterium atoms at the 2,2 positions enhances its utility in various scientific applications, particularly in metabolic studies and drug development. This article delves into the properties, applications, and market trends of this specialized compound, providing valuable insights for researchers and industry professionals.

The chemical structure of N-(3-Methylcrotonyl)glycine-2,2-d2 features a deuterium-labeled glycine moiety, which makes it an excellent tool for isotope labeling experiments. Deuterium, a stable isotope of hydrogen, is widely used in NMR spectroscopy and mass spectrometry to trace metabolic pathways and study reaction mechanisms. The compound's unique labeling pattern allows for precise tracking in complex biological systems, making it indispensable in proteomics research and biomarker discovery.

One of the most compelling applications of N-(3-Methylcrotonyl)glycine-2,2-d2 is in the field of metabolic engineering. Researchers are increasingly focusing on understanding how cells metabolize specific compounds, and deuterated analogs like this one provide a clear advantage. For instance, recent studies have utilized this compound to investigate the catabolism of branched-chain amino acids, a topic of growing interest in nutritional science and personalized medicine. The ability to monitor these pathways with high precision has opened new avenues for developing targeted therapies.

In addition to its role in research, N-(3-Methylcrotonyl)glycine-2,2-d2 has garnered attention for its potential in drug formulation. Deuterated compounds are known to exhibit altered pharmacokinetic properties, such as improved metabolic stability and prolonged half-life. This has led to a surge in demand for deuterated building blocks in the pharmaceutical industry, particularly for the development of next-generation therapeutics. The compound's compatibility with high-throughput screening platforms further enhances its appeal for drug discovery programs.

The synthesis of N-(3-Methylcrotonyl)glycine-2,2-d2 involves sophisticated techniques to ensure high isotopic purity. Manufacturers employ advanced deuterium incorporation methods, such as catalytic exchange or custom synthetic routes, to achieve the desired labeling efficiency. Quality control is paramount, as even minor impurities can skew experimental results. As a result, suppliers of this compound often provide detailed certificates of analysis, including data on isotopic enrichment and chemical purity.

Market trends indicate a rising demand for deuterated compounds like N-(3-Methylcrotonyl)glycine-2,2-d2, driven by advancements in analytical technologies and the expanding scope of precision medicine. The global market for isotope-labeled reagents is projected to grow significantly, with applications spanning academia, biotechnology, and pharmaceuticals. Researchers are particularly interested in how these compounds can facilitate translational research, bridging the gap between laboratory findings and clinical applications.

For those seeking to purchase N-(3-Methylcrotonyl)glycine-2,2-d2, it is essential to source the compound from reputable suppliers who adhere to stringent quality standards. Key considerations include isotopic purity, batch-to-batch consistency, and compliance with regulatory guidelines. Many suppliers offer custom synthesis services, allowing researchers to obtain compounds tailored to their specific needs, such as different levels of deuterium incorporation or modified functional groups.

In summary, N-(3-Methylcrotonyl)glycine-2,2-d2 (CAS No. 1276197-31-9) is a versatile and valuable tool in modern scientific research. Its applications in metabolic studies, drug development, and analytical chemistry underscore its importance in advancing our understanding of biological systems. As the demand for deuterated compounds continues to rise, this compound is poised to play a pivotal role in shaping the future of life sciences and pharmaceutical innovation.

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