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-010726 |
CAS: 19136-92-6 |
Molecular Formula: C4H6D2O2 |
Molecular Weight: 90.12 |
Chemical Structure |
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Synonyms | Butyric-2,2-d2 Acid; Butanoic Acid-2,2-d2; 1-Propanecarboxylic Acid-2,2-d2; Ethylacetic Acid-2,2-d2; Honey Robber-2,2-d2; NSC 8415-2,2-d2; Propylformic Acid-2,2-d2; n-Butanoic Acid-2,2-d2; n-Butyric Acid-2,2-d2 |
IUPAC Name | 2,2-dideuteriobutanoic acid |
Related CAS | 107-92-6 (unlabelled) |
Canonical SMILES | CCCC(=O)O |
InChI | InChI=1S/C4H8O2/c1-2-3-4(5)6/h2-3H2,1H3,(H,5,6)/i3D2 |
InChI Key | FERIUCNNQQJTOY-SMZGMGDZSA-N |
Purity | 98%; 98% atom D |
Appearance | Liquid |
Storage | Store at -20°C |
Butyric Acid-[2,2-d2], a specialized form of butyric acid with a distinctive isotopic composition, finds extensive utility in diverse research and analytical fields. Here are key applications of Butyric Acid-[2,2-d2] presented with heightened perplexity and burstiness:
Stable Isotope Tracing: Central to metabolic investigations, Butyric Acid-[2,2-d2] is a cornerstone in tracing the intricate metabolic pathways of butyrate within biological systems. By meticulously monitoring the trajectory and transformation of deuterium-labeled butyrate, researchers delve into the realms of cellular energy production and lipid metabolism, shedding light on diseases like cancer, where metabolic pathways undergo profound alterations.
NMR Spectroscopy: In the realm of nuclear magnetic resonance (NMR) spectroscopy, Butyric Acid-[2,2-d2] assumes a pivotal role as an internal standard and reference compound owing to its distinct isotopic fingerprint. This characteristic enables exceptionally precise quantitative analysis of butyrate and its derivatives within complex mixtures, facilitating the exploration of molecular structures and dynamics across diverse chemical and biological domains.
Gut Microbiome Research: With a significant impact on gut health, butyric acid is a key player in gut microbiota research, particularly when utilized in its deuterated form, Butyric Acid-[2,2-d2]. By studying the production and utilization of butyrate by gut microbes, scientists unravel the metabolic intricacies across different microbial species, paving the way for strategies to modulate the gut microbiome for enhanced health outcomes. This exploration bridges connections between dietary patterns, microbiota composition, and systemic health conditions.
Food Science and Nutrition: Unveiling the mysteries of flavor profiles and butyrate formation during fermentation processes, Butyric Acid-[2,2-d2] emerges as a critical tool in the realm of food science. Its presence aids in unraveling the pathways leading to butyrate generation in dairy and other fermented products, contributing to enhanced understanding of these mechanisms and potentially fostering the development of functional foods with not just palatable flavors, but also inherent health benefits.
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