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-006711 |
Molecular Formula: C10[13C]6H13N |
Molecular Weight: 225.24 |
Chemical Structure |
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IUPAC Name | N-(phenyl-13C6)naphthalen-1-amine |
Related CAS | 90-30-2 (unlabelled) |
Canonical SMILES | C1=CC=C(C=C1)NC2=CC=CC3=CC=CC=C32 |
InChI | InChI=1S/C16H13N/c1-2-9-14(10-3-1)17-16-12-6-8-13-7-4-5-11-15(13)16/h1-12,17H/i1+1,2+1,3+1,9+1,10+1,14+1 |
InChI Key | XQVWYOYUZDUNRW-UTVSNGSCSA-N |
Purity | 98% by CP; 98% atom 13C |
Solubility | Soluble in Chloroform, Methanol |
Storage | Store at -20°C |
N-Phenyl-1-Naphthylamine-[13C6], a stable isotopically labeled compound, is a versatile asset in scientific research and industrial applications. Here are key applications presented with high perplexity and burstiness:
Stable Isotope Tracing: Serving as a cornerstone in metabolic investigations, N-Phenyl-1-Naphthylamine-[13C6] emerges as a tracer, illuminating the intricate pathways of biochemistry. Integrating this labeled compound into experiments, scientists embark on a journey to unveil the dynamic movement and transformation of molecules within living systems. This data unveils profound insights into metabolic processes, offering a glimpse into the fate of chemical compounds within biological organisms.
Spectroscopic Analysis: Within the domain of analytical chemistry, N-Phenyl-1-Naphthylamine-[13C6] assumes a pivotal role as an essential internal standard for mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy. The distinctive isotopic pattern aids in precise quantification and definitive identification of analytes amidst complex mixtures. This meticulous approach ensures the accuracy and robustness of analytical outcomes, particularly in quantitating closely related compounds.
Reference Material: Standing as a beacon of excellence in analytical instruments, this compound serves as a high-quality reference material critical for calibration purposes. By utilizing a known standard endowed with a unique isotopic label, laboratories can routinely verify the performance of their measurement systems. This practice promotes consistency and upholds measurement practices in accordance with global standards and regulations, guaranteeing unwavering precision.
Chemical Research: Unveiling the mysteries of organic chemistry, N-Phenyl-1-Naphthylamine-[13C6] plays a pivotal role in mechanistic studies, guiding researchers through the intricate dance of chemical transformations. Scientists leverage this compound to delve into reaction mechanisms, meticulously tracing isotopic labels as they navigate through diverse chemical metamorphoses. This detailed perspective empowers researchers to unravel the complex steps of transformations, paving the way for optimized reactions and exploration of novel synthetic pathways.
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