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Perfluorononanoic Acid-[13C9]

General Information
Catalog: BLP-008604
Molecular Formula: [13C]9HF17O2
Molecular Weight: 473.01
Chemical Structure
Perfluorononanoic Acid-[13C9]
Description Perfluorononanoic Acid-[13C9] is the isotope labelled analog of Perfluorononanoic Acid. Perfluorinated compounds (PFCs) are persistent in environments due to the high energy of C-F bond. It is a persistent environmental pollutant.
Synonyms 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,9-Heptadecafluorononanoic Acid-13C9; Heptadecafluorononanoic Acid-13C9; Perfluorononanoic Acid-13C9; Perfluoropelargonic Acid-13C9; PFNA-13C9
Related CAS 375-95-1 (unlabelled)
Purity 97% by CP; 98% atom 13C

Perfluorononanoic Acid-[13C9], a stable isotopic labeled compound, is of significant importance in analytical and research fields. Here are key applications with a high degree of perplexity and burstiness:

Environmental Monitoring: Serving as a crucial internal standard, Perfluorononanoic Acid-[13C9] plays a vital role in analyzing per- and polyfluoroalkyl substances (PFAS) in environmental samples. Its isotopic labeling ensures precise quantification of PFAS in water, soil, and biota, providing robust data necessary for regulatory compliance and environmental risk assessment. This is paramount in comprehending the distribution and implications of PFAS contamination in the environment.

Pharmacokinetics Studies: In the realm of pharmaceutical research, Perfluorononanoic Acid-[13C9] acts as a tracer for investigating the absorption, distribution, metabolism, and excretion of PFAS in biological systems. By tracing the isotopically labeled compound, researchers gain profound insights into the pharmacokinetics and bioaccumulation of PFAS in organisms. Such detailed information is crucial for assessing human exposure and potential health risks associated with these substances.

Chemical Reaction Tracing: Employed in exploring chemical reaction mechanisms and pathways, Perfluorononanoic Acid-[13C9] empowers researchers to monitor and quantify the conversion of perfluorinated compounds in various chemical processes. Its unique isotopic composition enables the tracing of degradation pathways and transformation products in both industrial and environmental chemistry settings. This application proves particularly valuable for unraveling intricate chemical processes.

Toxicological Research: In toxicological investigations, Perfluorononanoic Acid-[13C9] is utilized to evaluate the toxic impacts of PFAS on biological systems. By incorporating the isotopic label, researchers can accurately assess exposure levels and correlate them with biological responses. This enhanced understanding of PFAS’ toxicokinetics assists in shaping risk assessments and regulatory guidelines, facilitating informed decision-making in toxicological research.

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