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Catalog Number:
04952
CAS Number:
204316-10-9
Sel de dicyclohexylammonium de l'acide Fmoc-(3 S ,4 S )-4-amino-3-hydroxy-5-méthylhexanoïque
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-AHMHxA(3 S ,4 S )-OH·DCHA
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$120.88 /100 mg
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Product Information

Fmoc-(3S,4S)-4-amino-3-hydroxy-5-methylhexanoic acid dicyclohexylammonium salt is a versatile compound widely utilized in peptide synthesis and drug development. This compound, often referred to as Fmoc-Amino Acid, serves as a crucial building block in the formation of peptides, enabling researchers to create complex structures with high specificity. Its unique Fmoc (9-fluorenylmethyloxycarbonyl) protective group allows for easy removal under mild conditions, making it an ideal choice for sensitive applications in organic synthesis and medicinal chemistry.

The dicyclohexylammonium salt form enhances solubility and stability, facilitating its use in various solvents and reaction conditions. This compound is particularly beneficial in the pharmaceutical industry for the development of peptide-based therapeutics, where precision and efficiency are paramount. Additionally, its application extends to the field of biochemistry, where it aids in the study of protein interactions and functions. With its favorable properties and broad applicability, Fmoc-(3S,4S)-4-amino-3-hydroxy-5-methylhexanoic acid dicyclohexylammonium salt is an essential tool for researchers aiming to innovate in peptide synthesis and drug formulation.

Synonyms
Fmoc-AHMHxA(3 S ,4 S )-OH·DCHA
CAS Number
204316-10-9
Purity
≥ 97 % (HPLC)
Molecular Formula
C 22 H 25 NO 5 · C 12 H 23 N
Molecular Weight
564.8
MDL Number
MFCD00270198
PubChem ID
78292184
Appearance
Solide blanc
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-AHMHxA(3 S ,4 S )-OH·DCHA
CAS Number
204316-10-9
Purity
≥ 97 % (HPLC)
Molecular Formula
C 22 H 25 NO 5 · C 12 H 23 N
Molecular Weight
564.8
MDL Number
MFCD00270198
PubChem ID
78292184
Appearance
Solide blanc
Conditions
Conserver à 0-8 °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-5-methylhexanoic acid dicyclohexylammonium salt is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for easy removal during the synthesis process, making it a preferred choice for researchers.
  • Drug Development: In pharmaceutical research, it is used to create novel peptide-based drugs. Its unique structure can enhance the bioactivity of therapeutic peptides, providing potential advantages in targeting specific biological pathways.
  • Bioconjugation: The compound is effective in bioconjugation applications, where it can be linked to various biomolecules. This is particularly useful in developing targeted drug delivery systems, improving the efficacy of treatments.
  • Research in Neuroscience: Its derivatives may be explored for their effects on neurological pathways, aiding in the development of treatments for neurodegenerative diseases. This application highlights its potential in advancing medical research.
  • Material Science: The compound can be incorporated into polymer systems to enhance their properties, such as biocompatibility and mechanical strength, making it valuable in the development of biomedical materials.

Citations