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Catalog Number:
02490
CAS Number:
88574-06-5
Fmoc-6-aminohexanoic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-6-aminocaproic acid, Fmoc-ε-Ahx-OH
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$20.20 /1G
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Product Information

Fmoc-6-aminohexanoic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (fluorenylmethyloxycarbonyl) group, which allows for selective deprotection during the synthesis of peptides, making it an essential tool for researchers in the field of medicinal chemistry. Its unique structure enhances solubility and stability, facilitating the formation of complex peptide sequences.

In practical applications, Fmoc-6-aminohexanoic acid is particularly valuable in the development of peptide-based therapeutics and biomaterials. Its ability to serve as a linker in solid-phase peptide synthesis enables the efficient assembly of peptides with specific biological activities. Additionally, this compound is recognized for its role in the design of drug delivery systems and targeted therapies, providing researchers with innovative solutions for enhancing drug efficacy. With its favorable properties and wide-ranging applications, Fmoc-6-aminohexanoic acid is an indispensable asset for professionals in pharmaceutical and biochemical research.

Synonyms
Fmoc-6-aminocaproic acid, Fmoc-ε-Ahx-OH
CAS Number
88574-06-5
Purity
≥ 99% (HPLC)
Molecular Formula
C21H23NO4
Molecular Weight
353.3
MDL Number
MFCD00077045
PubChem ID
2756087
Melting Point
110 - 123 °C
Appearance
White powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-6-aminocaproic acid, Fmoc-ε-Ahx-OH
CAS Number
88574-06-5
Purity
≥ 99% (HPLC)
Molecular Formula
C21H23NO4
Molecular Weight
353.3
MDL Number
MFCD00077045
PubChem ID
2756087
Melting Point
110 - 123 °C
Appearance
White powder
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-6-aminohexanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It is used in the design of peptide-based drugs, enhancing the stability and bioavailability of therapeutic peptides, which is crucial in pharmaceutical applications.
  • Bioconjugation: The compound facilitates the attachment of biomolecules to surfaces or other molecules, improving the efficacy of diagnostics and targeted drug delivery systems.
  • Research in Biochemistry: Researchers employ it in the study of protein interactions and functions, aiding in the understanding of biological processes and disease mechanisms.
  • Material Science: It finds applications in creating functionalized polymers and materials, which can be tailored for specific uses in coatings, adhesives, and drug delivery systems.

Citations