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L-Phenylalanine-[2-13C]

General Information
Catalog: BLP-009083
CAS: 136056-01-4
Molecular Formula: C8[13C]H11NO2
Molecular Weight: 166.18
Chemical Structure
L-Phenylalanine-[2-13C]
Description L-Phenylalanine-[2-13C] is the isotope form of L-phenylalanine. L-Phenylalanine is an essential amino acid that is important for the biosynthesis of other amino acids including melanin, dopamine, noradrenalin and thyroxine.
Synonyms L-Phenylalanine-2-13C
IUPAC Name (2S)-2-amino-3-phenyl(2-13C)propanoic acid
Related CAS 63-91-2 (unlabelled)
Canonical SMILES C1=CC=C(C=C1)CC(C(=O)O)N
InChI InChI=1S/C9H11NO2/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12)/t8-/m0/s1/i8+1
InChI Key COLNVLDHVKWLRT-IDMPRHEVSA-N
Purity 98% by CP; 99% atom 13C
Solubility Soluble in DMSO, Water
Appearance White to Off-white Solid
Storage Store at -20°C

L-Phenylalanine-[2-13C], an isotopically labeled version of the amino acid phenylalanine, finds extensive use in diverse scientific research applications. Here are the key applications of L-Phenylalanine-[2-13C]:

Metabolic Tracing: Delving into metabolic tracing studies, L-Phenylalanine-[2-13C] unlocks insights into the intricate pathways governing phenylalanine catabolism and anabolism. By meticulously tracking the 13C label, researchers unravel the processing and utilization of phenylalanine across varied biological systems. This exploration sheds light on amino acid metabolism, disease states, and potential therapeutic strategies, offering a deeper understanding of physiological processes.

Nutritional Studies: In the realm of nutritional research, L-Phenylalanine-[2-13C] serves as a critical tool for investigating the digestion, absorption, and utilization of phenylalanine within the human body. Through the administration of this labeled compound, scientists monitor its integration into proteins and other biomolecules, enriching our knowledge of dietary requirements and the repercussions of nutritional imbalances. This exploration aids in comprehending the complexities of human nutrition and metabolic health.

Protein Synthesis Research: Unlocking the realms of protein synthesis, L-Phenylalanine-[2-13C] emerges as a valuable asset for scrutinizing the rates of synthesis and turnover within diverse tissues. By incorporating this labeled amino acid into cell cultures or animal models, researchers uncover the kinetics of protein generation and breakdown, offering insights into cellular dynamics, growth processes, and responses to external stimuli. This investigation enhances our grasp of fundamental biological processes and the intricacies of protein regulation.

Medical Diagnostics: In the domain of medical diagnostics, L-Phenylalanine-[2-13C] plays a pivotal role, particularly in advanced imaging techniques like Magnetic Resonance Spectroscopy (MRS). Through the introduction of labeled phenylalanine, practitioners gain a window into metabolic processes, enabling the detection of anomalies in tissues such as the brain. This diagnostic capability proves invaluable in identifying metabolic disorders, monitoring disease progression, and guiding personalized treatment approaches, showcasing the convergence of cutting-edge science and clinical practice.

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