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Catalog Number:
42547
CAS Number:
478706-50-2
Ácido ( S )-Fmoc-2-amino-tetradecanoico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Ácido (2 S )-2-(Fmoc-amino)tetradecanoico, Fmoc-L-2Atado-OH
Documents
$75.00 /5 mg
Tamaño
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Product Information

(S)-Fmoc-2-amino-tetradecanoic acid is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is crucial for the selective protection of amino groups during the synthesis of peptides. Its long aliphatic chain enhances hydrophobic interactions, making it particularly beneficial in the design of bioactive peptides and pharmaceuticals. Researchers appreciate its stability and ease of use in solid-phase peptide synthesis, where it facilitates the formation of complex peptide structures with high purity and yield.

In addition to its applications in peptide synthesis, (S)-Fmoc-2-amino-tetradecanoic acid is also employed in the development of surfactants and emulsifiers due to its amphiphilic nature. This compound's unique properties allow for the creation of tailored materials in drug delivery systems, enhancing the bioavailability of therapeutic agents. Its ability to form stable complexes with various biomolecules further underscores its significance in biochemical research and pharmaceutical formulations.

Synonyms
Ácido (2 S )-2-(Fmoc-amino)tetradecanoico, Fmoc-L-2Atado-OH
CAS Number
478706-50-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C 29 H 39 N.º 4
Molecular Weight
465.62
MDL Number
MFCD08275903
PubChem ID
2756197
Melting Point
94 - 96 °C
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -10 ± 1 ° (C=1 en DMF)
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Ácido (2 S )-2-(Fmoc-amino)tetradecanoico, Fmoc-L-2Atado-OH
CAS Number
478706-50-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C 29 H 39 N.º 4
Molecular Weight
465.62
MDL Number
MFCD08275903
PubChem ID
2756197
Melting Point
94 - 96 °C
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -10 ± 1 ° (C=1 en DMF)
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-Fmoc-2-amino-tetradecanoic acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create specific sequences for studies in biochemistry and molecular biology.
  • Drug Development: It plays a crucial role in the pharmaceutical industry for developing new drugs, particularly in creating peptide-based therapeutics that target specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of peptides to various biomolecules, enhancing the efficacy of drug delivery systems.
  • Protein Engineering: In protein engineering, it aids in modifying proteins to improve their stability and functionality, which is essential for developing better diagnostic tools and therapeutics.
  • Research in Neuroscience: This chemical is valuable in neuroscience research, particularly in studying neuropeptides and their roles in signaling pathways, contributing to advancements in understanding neurological disorders.

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