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Catalog Number:
11967
CAS Number:
111061-54-2
N α -Fmoc- N ε -tritil-L-lisina
Purity:
≥ 99,8 % (HPLC quiral)
Synonym(s):
Fmoc-L-Lys(Trt)-OH
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Product Information

Na-Fmoc-Ne-trityl-L-lysine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which is essential for the selective protection of the amino group during the synthesis of complex peptides. The trityl group enhances stability and solubility, making it an ideal choice for researchers focused on solid-phase peptide synthesis. Its unique structure allows for efficient coupling reactions, facilitating the creation of diverse peptide libraries that are crucial in pharmaceutical research and development.

In addition to its role in peptide synthesis, Na-Fmoc-Ne-trityl-L-lysine is also valuable in the study of protein interactions and the development of novel therapeutics. Its ability to provide stability and protect functional groups makes it a preferred choice for chemists looking to explore new drug candidates or optimize existing ones. With its proven efficacy and reliability, this compound is an essential tool for researchers aiming to advance their work in biochemistry and medicinal chemistry.

Synonyms
Fmoc-L-Lys(Trt)-OH
CAS Number
111061-54-2
Purity
≥ 99,8 % (HPLC quiral)
Molecular Formula
C40H38N2O4
Molecular Weight
610.75
MDL Number
MFCD00270545
PubChem ID
13943556
Melting Point
126 - 133 ?C
Appearance
Cristales de color blanco a blanquecino
Optical Rotation
[a] D 20 = 5 ± 1 º (C=2 en CHCl 3 )
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L-Lys(Trt)-OH
CAS Number
111061-54-2
Purity
≥ 99,8 % (HPLC quiral)
Molecular Formula
C40H38N2O4
Molecular Weight
610.75
MDL Number
MFCD00270545
PubChem ID
13943556
Melting Point
126 - 133 ?C
Appearance
Cristales de color blanco a blanquecino
Optical Rotation
[a] D 20 = 5 ± 1 º (C=2 en CHCl 3 )
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Fmoc-Ne-trityl-L-lysine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interference from other functional groups.
  • Drug Development: Its application in the design of peptide-based drugs enhances stability and bioavailability, making it valuable in pharmaceutical research.
  • Bioconjugation: The compound is used to attach peptides to various biomolecules, facilitating the development of targeted therapies in cancer treatment and diagnostics.
  • Protein Engineering: Researchers utilize it to create modified proteins with enhanced properties, aiding in the study of protein function and interactions.
  • Research in Neuroscience: Its role in synthesizing neuropeptides allows for the exploration of neurological pathways, contributing to advancements in understanding brain function and disorders.

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