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L-Phenylalanine-OH-13C9,15N, Fmoc

Chemical Name L-Phenylalanine-OH-13C9,15N, Fmoc
CAT No. CS-CH-00150
CAS No. 1217455-27-0
Status price
Category Stable Isotopes
Hazardous This is not a Hazardous Compound
COA View Sample COA
Controlled No

Additional Information


Packing Product will be supplied in Vials, in certain conditions we also use 'Septa Vials'
Controlled No
Parent API Phenylalanine
Smileys O=C([15NH][13C@H]([13C](O)=O)[13CH2][13C]1=[13CH][13CH]=[13CH][13CH]=[13CH]1)OCC2C3=CC=CC=C3C4=CC=CC=C24
Hazardous No


Usage and description


L-Phenylalanine-OH-13C9,15N, Fmoc is a modified form of the amino acid L-Phenylalanine. It is commonly used in the field of organic chemistry and biochemistry research. The chemical formula of L-Phenylalanine-OH-13C9,15N, Fmoc is C27H26N2O5 and it has a molecular weight of 466.51 g/mol. The addition of the isotopes 13C and 15N to L-Phenylalanine-OH-13C9,15N, Fmoc allows for more precise analysis of protein structures and their interactions. This is because the isotopes create a unique signature that can be detected and measured using various analytical techniques including NMR spectroscopy and mass spectrometry. Fmoc (9-fluorenylmethoxycarbonyl) is a common protective group used in peptide synthesis to protect the amino group of an amino acid. It is added to L-Phenylalanine-OH-13C9,15N to prevent unwanted reactions during the peptide synthesis process. L-Phenylalanine-OH-13C9,15N, Fmoc has a wide range of applications in biological research, including the study of protein structure, protein-protein interactions, and protein-ligand interactions. It is also used in the development of new drugs and therapies for various diseases. Overall, L-Phenylalanine-OH-13C9,15N, Fmoc is a valuable tool for researchers in the field of biochemistry and organic chemistry.

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