4-Hydroxyphenyllactic acid-[13C6] (racemic mixture)

General Information
Catalog: BLP-006523
Molecular Formula: C3[13C]6H10O4
Molecular Weight: 188.13

General Information

Catalog: BLP-006523

Molecular Formula: C3[13C]6H10O4

Molecular Weight: 188.13

Chemical Structure

Synonyms	[U-Ring-13C6]-4-Hydroxyphenyllactic acid, racemic mixture; 2-Hydroxy-3-(4-hydroxyphenyl)propanoic acid-13C6; 3-(4-Hydroxyphenyl)lactic acid-13C6; HPLA-13C6; 4-Hydroxyphenyllactic acid-13C6; Hydroxyphenyllactic acid-13C6; dl-p-Hydroxyphenyllactic acid-13C6; 2-Hydroxy-3-(p-hydroxyphenyl)propionic acid-13C6; beta-(p-Hydroxyphenyl)lactic acid-13C6; p-Hydroxyphenyl lactic acid-13C6; DL-4-Hydroxyphenyllactic Acid-13C6
IUPAC Name	2-hydroxy-3-(4-hydroxy(1,2,3,4,5,6-13C6)cyclohexa-1,3,5-trien-1-yl)propanoic acid
Related CAS	306-23-0 (unlabelled)
Canonical SMILES	C1=CC(=CC=C1CC(C(=O)O)O)O
InChI	InChI=1S/C9H10O4/c10-7-3-1-6(2-4-7)5-8(11)9(12)13/h1-4,8,10-11H,5H2,(H,12,13)/i1+1,2+1,3+1,4+1,6+1,7+1
InChI Key	JVGVDSSUAVXRDY-ZFJHNFROSA-N
Purity	98%
Solubility	Slightly soluble in DMSO, Methanol
Appearance	White Solid
Storage	Store at -20°C

4-Hydroxyphenyllactic acid-[13C6] (racemic mixture) is a labeled compound utilized in diverse research contexts, particularly for investigating metabolic processes. Here are key applications of 4-Hydroxyphenyllactic acid-[13C6] presented with high perplexity and burstiness:

Metabolic Flux Analysis: This labeled compound serves as a valuable tool for tracing metabolic pathways in comprehensive metabolic flux analysis. By integrating 4-Hydroxyphenyllactic acid-[13C6] into metabolic investigations, researchers can gain insights into the intricate utilization and distribution of carbon atoms across various pathways. This understanding is pivotal for unraveling the complexities of cellular metabolism and fine-tuning biotechnological processes.

Stable Isotope Labeling: In the realms of proteomics and metabolomics, 4-Hydroxyphenyllactic acid-[13C6] acts as a stable isotope label employed to examine metabolic alterations within cells. It enables scientists to monitor the integration of labeled metabolites into cellular components, facilitating the analysis of metabolite turnover and dynamic metabolic processes. This application aids in the identification of biomarkers and sheds light on underlying disease mechanisms.

Pharmaceutical Research: Playing a significant role in pharmaceutical research, this isotopically labeled compound aids in the investigation of drug metabolism and pharmacokinetics. By utilizing 4-Hydroxyphenyllactic acid-[13C6], researchers can delve into the mechanisms of drug processing within the body and identify metabolic byproducts. This knowledge is crucial for advancing drug development and enhancing therapeutic effectiveness.

Chemical Synthesis Studies: Within the realm of chemical synthesis research, 4-Hydroxyphenyllactic acid-[13C6] acts as a precursor or intermediate for synthesizing complex molecules. Its labeled carbon atoms provide a means to monitor reactions and intermediate formations along synthetic pathways. This application facilitates a deeper understanding of reaction mechanisms and enables the optimization of synthetic routes, pushing the boundaries of synthetic chemistry exploration.