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Catalog Number:
29696
CAS Number:
1310680-47-7
Acide ( S )-Fmoc-2-amino-3-éthyl-pentanoïque
Purity:
≥ 99,5 % (HPLC chirale)
Documents
$185.68 /100 mg
Taille
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Product Information

(S)-Fmoc-2-amino-3-ethyl-pentanoic acid is a valuable building block in peptide synthesis, particularly favored in the development of pharmaceuticals and biotechnological applications. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which allows for selective deprotection during the synthesis process, making it an essential tool for chemists working on complex peptide sequences. Its unique structure not only enhances solubility but also provides stability during reactions, which is crucial for maintaining the integrity of sensitive compounds.

Researchers and industry professionals utilize (S)-Fmoc-2-amino-3-ethyl-pentanoic acid in the synthesis of various bioactive peptides, including those used in drug development and therapeutic applications. Its ability to facilitate the formation of peptide bonds while maintaining high purity levels makes it a preferred choice in laboratories focused on peptide chemistry. Additionally, this compound's compatibility with automated synthesizers streamlines the production process, enhancing efficiency and reducing time-to-market for new therapeutic agents.

CAS Number
1310680-47-7
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C 22 H 254
Molecular Weight
367.44
MDL Number
MFCD11226813
PubChem ID
75110601
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0 - 8 °C
General Information
CAS Number
1310680-47-7
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C 22 H 254
Molecular Weight
367.44
MDL Number
MFCD11226813
PubChem ID
75110601
Appearance
Poudre blanche à blanc cassé
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

(S)-Fmoc-2-amino-3-ethyl-pentanoic acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a crucial building block in the synthesis of peptides, particularly in solid-phase peptide synthesis. Its protective Fmoc group allows for selective deprotection, facilitating the assembly of complex peptide sequences.
  • Drug Development: In pharmaceutical research, it is used to create peptide-based drugs, which can offer targeted therapies with fewer side effects compared to traditional small-molecule drugs. This specificity is particularly beneficial in oncology and autoimmune diseases.
  • Bioconjugation: The compound is employed in bioconjugation techniques, where it helps attach peptides to other biomolecules, enhancing the delivery and efficacy of therapeutic agents in targeted drug delivery systems.
  • Research in Neuroscience: It is utilized in studying neuropeptides, which play a significant role in brain function and behavior. Understanding these peptides can lead to advancements in treating neurological disorders.
  • Protein Engineering: The compound aids in the design of modified proteins with enhanced stability and activity, which is essential in developing biocatalysts and therapeutic proteins for industrial applications.

Citations