🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
04950
CAS Number:
215190-17-3
Ácido Fmoc-(3 S ,4 S ,5 S -4-amino-3-hidroxi-5-metilheptanoico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-AHMHpA( 3S , 4S ,5S - OH)
Documents
$120.88 /100 mg
Tamaño
Request Bulk Quote
Product Information

Fmoc-(3S,4S,5S)-4-amino-3-hydroxy-5-methylheptanoic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound, known for its protective Fmoc (fluorenylmethyloxycarbonyl) group, facilitates the selective modification of amino acids, making it an essential reagent in the development of peptide-based therapeutics. Its unique structure, featuring a hydroxyl group and a branched alkyl chain, enhances solubility and stability, which are critical for successful synthesis and purification processes.

Researchers and industry professionals benefit from its application in the synthesis of bioactive peptides, including those used in drug discovery and development. The compound's ability to improve the yield and purity of synthesized peptides makes it a preferred choice in laboratories focused on peptide research. Additionally, its compatibility with various coupling reagents allows for streamlined workflows in peptide assembly, thereby accelerating the pace of research and innovation in pharmaceutical applications.

Synonyms
Fmoc-AHMHpA( 3S , 4S ,5S - OH)
CAS Number
215190-17-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C23H27Nº 5
Molecular Weight
397.48
MDL Number
MFCD00270207
PubChem ID
4712569
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-AHMHpA( 3S , 4S ,5S - OH)
CAS Number
215190-17-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C23H27Nº 5
Molecular Weight
397.48
MDL Number
MFCD00270207
PubChem ID
4712569
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(3S,4S,5S)-4-amino-3-hydroxy-5-methylheptanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It plays a critical role in the design of novel pharmaceuticals, particularly in creating compounds that target specific biological pathways, enhancing therapeutic efficacy.
  • Biotechnology: Used in the production of biologically active peptides, it supports advancements in biotechnology applications, including vaccine development and enzyme engineering.
  • Research in Neuroscience: The compound is valuable in studying neuropeptides, contributing to a better understanding of neurological functions and potential treatments for neurodegenerative diseases.
  • Cosmetic Formulations: Its properties are leveraged in the formulation of skin care products, where it can enhance skin hydration and promote cellular regeneration.

Citas