Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
02408
CAS Number:
71989-21-4
Fmoc-L-glutamine 4-nitrophenyl ester
Synonym(s):
Fmoc-L-Gln-ONp
Documents
$45.47 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

Fmoc-L-glutamine 4-nitrophenyl ester is a versatile compound widely utilized in peptide synthesis and bioconjugation applications. This derivative of L-glutamine features a protective Fmoc (9-fluorenylmethoxycarbonyl) group, which facilitates the selective coupling of amino acids in solid-phase peptide synthesis. The presence of the 4-nitrophenyl ester moiety enhances its reactivity, making it an excellent choice for researchers aiming to create complex peptide structures with precision.

In the pharmaceutical and biotechnology sectors, Fmoc-L-glutamine 4-nitrophenyl ester serves as a key building block for the development of peptide-based therapeutics and diagnostic agents. Its unique properties allow for improved yields and purity in peptide synthesis, which is crucial for the production of high-quality biopharmaceuticals. Additionally, its compatibility with various coupling reagents and conditions makes it a preferred choice among professionals seeking efficiency and reliability in their synthetic processes.

Synonyms
Fmoc-L-Gln-ONp
CAS Number
71989-21-4
Molecular Formula
C26H23N3O7
Molecular Weight
489.5
MDL Number
MFCD00057763
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-L-Gln-ONp
CAS Number
71989-21-4
Molecular Formula
C26H23N3O7
Molecular Weight
489.5
MDL Number
MFCD00057763
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-L-glutamine 4-nitrophenyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing for the incorporation of glutamine residues. Its protective Fmoc group simplifies the process of sequential amino acid addition.
  • Drug Development: Researchers use this ester in the design of peptide-based pharmaceuticals, particularly in developing drugs targeting specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The compound is valuable in bioconjugation techniques, enabling the attachment of peptides to various biomolecules, which is crucial for creating targeted drug delivery systems.
  • Protein Engineering: In the field of protein engineering, it aids in modifying proteins to improve their stability and functionality, which is essential for biotechnological applications.
  • Analytical Chemistry: This chemical is utilized in analytical methods to study protein interactions and dynamics, providing insights into biological processes and potential therapeutic targets.

Citations