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Catalog Number:
02455
CAS Number:
158257-40-0
Acide Fmoc-(3 S ,4 S )-4-amino-3-hydroxy-6-méthylheptanoïque
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-Sta( 3S , 4S )-OH, Acide (3 S ,4 S )-4-(Fmoc-amino)-3-hydroxy-6-méthylheptanoïque
Documents
$95.00 /250 mg
Taille
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Product Information

Fmoc-(3S,4S)-4-amino-3-hydroxy-6-methylheptanoic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protective group, which is essential for the selective protection of amino acids during solid-phase peptide synthesis. Its unique structure, characterized by a hydroxyl and amino group, enhances its reactivity and compatibility with various coupling agents, making it an ideal choice for researchers aiming to create complex peptide sequences.

In addition to its role in peptide synthesis, Fmoc-(3S,4S)-4-amino-3-hydroxy-6-methylheptanoic acid has potential applications in the development of pharmaceuticals and biologically active compounds. Its ability to facilitate the formation of peptide bonds while maintaining stability under standard reaction conditions makes it a valuable asset in medicinal chemistry. Researchers can leverage this compound to explore new therapeutic avenues, particularly in the fields of oncology and infectious diseases, where peptide-based therapies are gaining traction.

Synonyms
Fmoc-Sta( 3S , 4S )-OH, Acide (3 S ,4 S )-4-(Fmoc-amino)-3-hydroxy-6-méthylheptanoïque
CAS Number
158257-40-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C 23 H 275
Molecular Weight
397.5
MDL Number
MFCD00065675
Appearance
Poudre blanche ou solide blanc
Optical Rotation
[a] D 25
Conditions
Conserver à ≤ -4 °C
General Information
Synonyms
Fmoc-Sta( 3S , 4S )-OH, Acide (3 S ,4 S )-4-(Fmoc-amino)-3-hydroxy-6-méthylheptanoïque
CAS Number
158257-40-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C 23 H 275
Molecular Weight
397.5
MDL Number
MFCD00065675
Appearance
Poudre blanche ou solide blanc
Optical Rotation
[a] D 25
Conditions
Conserver à ≤ -4 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-(3S,4S)-4-amino-3-hydroxy-6-methylheptanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, enhancing the efficiency and selectivity of peptide formation.
  • Drug Development: It plays a crucial role in the design of peptide-based therapeutics, particularly in targeting specific biological pathways, which can lead to more effective treatments.
  • Bioconjugation: The chemical is employed in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, facilitating drug delivery systems.
  • Analytical Chemistry: Its unique properties make it valuable in analytical methods for characterizing peptides and proteins, aiding in quality control and research validations.
  • Material Science: This compound is used in developing advanced materials with specific functionalities, such as hydrogels for biomedical applications, due to its biocompatibility.

Citations