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Heptanoic acid-[2,2,3,3-d4]

General Information
Catalog: BLP-008428
Molecular Formula: C7H10D4O2
Molecular Weight: 134.21
Chemical Structure
Heptanoic acid-[2,2,3,3-d4]
Description Heptanoic acid-[2,2,3,3-d4] is the labelled analogue of Heptanoic acid. Heptanoic acid is a straight-chain aliphatic carboxylic acid, used in the synthesis of esters for products such as fragrances and artificial flavor preparations.
Synonyms Heptanoic acid-d4
IUPAC Name 2,2,3,3-tetradeuterioheptanoic acid
Related CAS 111-14-8 (unlabelled)
Purity 98% by CP; 98% atom D
Storage Store at -20°C

Heptanoic acid-[2,2,3,3-d4], a deuterium-labeled compound with stable isotope characteristics, is instrumental in various scientific applications. Here are key applications of Heptanoic acid-[2,2,3,3-d4] presented with high perplexity and burstiness:

Mass Spectrometry Standards: Widely utilized as an internal standard in mass spectrometry, Heptanoic acid-[2,2,3,3-d4] facilitates precise quantification of compounds. The presence of deuterium atoms offers a clear distinction from natural heptanoic acid, ensuring accuracy in analysis. This application is indispensable in industries like pharmaceuticals and chemicals, where exact measurements are vital for quality control.

Metabolic Studies: In the realm of metabolic research, Heptanoic acid-[2,2,3,3-d4] acts as a tracer to explore fatty acid metabolism. By monitoring the integration and transformation of labeled heptanoic acid within metabolic pathways, researchers gain deeper insights into lipid metabolism. Such studies shed light on disorders linked to fatty acid metabolism and aid in the formulation of effective therapeutic interventions.

NMR Spectroscopy: Heptanoic acid-[2,2,3,3-d4] finds application in Nuclear Magnetic Resonance (NMR) spectroscopy for the examination of molecular structures and dynamics. The deuterium labeling simplifies the spectra, enhancing the interpretation of structural details. This utilization is particularly valuable in fields like organic chemistry and materials science for unraveling complex compound structures and behaviors.

Biochemical Research: Within the realm of biochemical investigations, Heptanoic acid-[2,2,3,3-d4] emerges as a vital tool for scrutinizing molecular interactions and mechanisms at a granular level. Its stability and distinctive isotopic signature make it ideal for studying enzyme activities and substrate engagements. These studies contribute significantly to our understanding of enzymatic functions and the potential interactions of drugs at a molecular level.

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