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Catalog Number:
15724
CAS Number:
1217731-48-0
Fmoc-D-2-amino-5-phenylpentanoic acid
Purity:
≥ 99% (HPLC, Chiral purity)
Synonym(s):
Fmoc-D-Nva(5-phenyl)-OH
Documents
$55.00 /250MG
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Product Information

Fmoc-D-2-amino-5-phenylpentanoic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino acids during solid-phase peptide synthesis. Its unique structure not only enhances the stability of the peptide chain but also facilitates the introduction of complex functionalities, making it an invaluable tool for researchers in the fields of medicinal chemistry and biochemistry.

With its high purity and reliable performance, Fmoc-D-2-amino-5-phenylpentanoic acid is ideal for applications in the development of therapeutic peptides and protein engineering. Researchers can leverage its properties to create novel compounds with improved bioactivity and specificity. This compound stands out due to its ability to enhance the solubility and stability of peptides, which is crucial for their efficacy in biological systems. Whether you are working on drug discovery or peptide-based therapeutics, this compound offers significant advantages over traditional amino acids, making it a preferred choice for professionals in the industry.

Synonyms
Fmoc-D-Nva(5-phenyl)-OH
CAS Number
1217731-48-0
Purity
≥ 99% (HPLC, Chiral purity)
Molecular Formula
C26H25NO4
Molecular Weight
415.49
MDL Number
MFCD04117842
PubChem ID
53398061
Appearance
White solid
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-D-Nva(5-phenyl)-OH
CAS Number
1217731-48-0
Purity
≥ 99% (HPLC, Chiral purity)
Molecular Formula
C26H25NO4
Molecular Weight
415.49
MDL Number
MFCD04117842
PubChem ID
53398061
Appearance
White solid
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-D-2-amino-5-phenylpentanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without affecting other functional groups.
  • Drug Development: Its unique structure aids in the design of bioactive peptides, which can lead to the development of new therapeutics for various diseases.
  • Bioconjugation: The compound is used in bioconjugation processes, facilitating the attachment of peptides to other biomolecules, enhancing the efficacy of drug delivery systems.
  • Research in Neuroscience: It plays a role in studying neuropeptides, which are crucial for understanding neurological functions and developing treatments for neurodegenerative diseases.
  • Analytical Chemistry: This chemical is employed in the analysis of peptide structures and functions, providing insights into protein interactions and stability.

Citations