Name: N-Carbobenzoxyglycine-[13C2,15N]
Brand: BOC Sciences
Rating: 5 (1 reviews)

General Information

Catalog: BLP-004932

CAS: 525587-92-2

Molecular Formula: C8[13C]2H11[15N]O4

Molecular Weight: 212.18

Chemical Structure

Synonyms	N-Carbobenzoxyglycine-13C2,15N; N-[(Phenylmethoxy)carbonyl]glycine-1,2-13C2,15N; N-Carboxyglycine N-Benzyl Ester-13C2,15N; N-Gly-OH-13C2,15N; (Carbobenzoxy)glycine-13C2,15N; 2-(Benzyloxycarbonylamino)acetic Acid-13C2,15N; N-(Benzyloxycarbonyl)glycine-13C2,15N; N-Cbz-glycine-13C2,15N; N-(α-Carbobenzoxy)glycine-13C2,15N; Z-Glycine-13C2,15N
IUPAC Name	((benzyloxy)carbonyl)glycine-13C2-15N
Related CAS	1138-80-3 (unlabelled)
Canonical SMILES	C1=CC=C(C=C1)COC(=O)NCC(=O)O
InChI	InChI=1S/C10H11NO4/c12-9(13)6-11-10(14)15-7-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,11,14)(H,12,13)/i6+1,9+1,11+1
InChI Key	CJUMAFVKTCBCJK-DYYXCFAWSA-N
Melting Point	117-119°C
Solubility	Slightly soluble in DMSO, Methanol
Appearance	White to Off-white Solid
Storage	Store at 2-8°C

N-Carbobenzoxyglycine-[13C2,15N], a compound labeled with stable isotopes, finds utility in diverse research realms. Here are key applications of N-Carbobenzoxyglycine-[13C2,15N] elucidated with high perplexity and burstiness:

Metabolic Flux Analysis: Deployed in metabolic flux analysis, N-Carbobenzoxyglycine-[13C2,15N] plays a pivotal role in tracing carbon and nitrogen cycles within biological systems. By tracking the labeled isotopes, researchers unveil profound insights into metabolic pathways and the flow of nutrients. This knowledge is imperative for comprehending cellular metabolism and optimizing processes in biotechnology and medicine.

Protein Structure and Dynamics: Delving into the realm of protein structure and dynamics, N-Carbobenzoxyglycine-[13C2,15N] is integrated into peptides and proteins. The presence of stable isotopes elevates resolution in nuclear magnetic resonance (NMR) spectroscopy, facilitating in-depth structural analysis. These insights are critical for drug design and decoding protein function within biological systems.

Environmental Studies: In the domain of environmental research, this compound serves to explore the destiny and metamorphosis of organic nitrogen in ecosystems. Through stable isotope tracing, scientists monitor the assimilation and turnover of nitrogen in soil and aquatic environments. This application aids in evaluating nutrient cycling, pollution impacts, and ecological dynamics.

Bioanalytical Chemistry: Acting as an internal standard in mass spectrometry-based quantitative analyses, N-Carbobenzoxyglycine-[13C2,15N] boasts a stable isotopic composition for precise quantification of glycine derivatives in intricate biological samples. This precision ensures accuracy and reliability in pharmacokinetic studies and metabolic profiling, enhancing the integrity of bioanalytical chemistry endeavors.