💛 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
29654
CAS Number:
1310680-22-8
Acide Fmoc-4-amino-4-méthyl-pentanoïque
Purity:
≥ 99 % (HPLC)
Documents
$127.79 /100 mg
Taille
Request Bulk Quote
Product Information

Fmoc-4-amino-4-methyl-pentanoic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (fluorenylmethyloxycarbonyl) group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure allows for the introduction of a branched side chain, enhancing the diversity and complexity of synthesized peptides. Researchers and industry professionals appreciate its stability and compatibility with various coupling reagents, making it an ideal choice for solid-phase peptide synthesis (SPPS) and other synthetic methodologies.

In addition to its role in peptide synthesis, Fmoc-4-amino-4-methyl-pentanoic acid has potential applications in the development of pharmaceuticals and biologically active compounds. Its ability to facilitate the incorporation of non-standard amino acids into peptide sequences opens new avenues for the design of novel therapeutics. The compound's favorable properties, such as its solubility and ease of handling, further contribute to its appeal in both academic and industrial settings. With its robust performance and adaptability, Fmoc-4-amino-4-methyl-pentanoic acid is an essential tool for researchers aiming to innovate in the field of peptide chemistry.

CAS Number
1310680-22-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C 21 H 234
Molecular Weight
353.42
MDL Number
MFCD18328458
PubChem ID
58382118
Melting Point
135-141 °C
Appearance
Poudre blanche
Conditions
Conserver à 0-8°C
General Information
CAS Number
1310680-22-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C 21 H 234
Molecular Weight
353.42
MDL Number
MFCD18328458
PubChem ID
58382118
Melting Point
135-141 °C
Appearance
Poudre blanche
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-4-amino-4-methyl-pentanoic 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 interfering with other functional groups.
  • Drug Development: Researchers leverage its properties to design and optimize peptide-based drugs, enhancing their stability and bioavailability in pharmaceutical formulations.
  • Bioconjugation: It is employed in bioconjugation techniques, facilitating the attachment of peptides to various biomolecules, which is crucial for developing targeted therapies and diagnostics.
  • Protein Engineering: The compound aids in the modification of proteins, improving their functionality and stability, which is essential in fields like biotechnology and enzyme engineering.
  • Research in Neuroscience: Its applications extend to neuroscience, where it is used to study neuropeptides, contributing to the understanding of neurological disorders and potential treatments.

Citations