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Catalog Number:
04010
CAS Number:
4530-18-1
Boc-DL-phenylalanine
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-DL-Phe-OH
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Product Information

Boc-DL-phenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a tert-butoxycarbonyl (Boc) protecting group, which enhances its stability and solubility, making it an ideal choice for the synthesis of complex peptides. Its unique structure allows for selective reactions, facilitating the incorporation of phenylalanine into various peptide sequences. Researchers appreciate its role in the development of therapeutic peptides, particularly in the fields of drug design and biochemistry, where precise amino acid modifications are crucial.

In addition to its applications in peptide synthesis, Boc-DL-phenylalanine serves as a valuable building block in the production of bioactive compounds and can be utilized in the development of novel drug candidates. Its ability to improve the pharmacokinetic properties of peptides makes it a preferred choice among professionals in medicinal chemistry. With its favorable characteristics, Boc-DL-phenylalanine stands out as a reliable compound for researchers aiming to innovate in peptide-based therapeutics.

Synonyms
Boc-DL-Phe-OH
CAS Number
4530-18-1
Purity
≥ 99% (HPLC)
Molecular Formula
C14H19NO4
Molecular Weight
265.31
MDL Number
MFCD00558969
PubChem ID
269698
Melting Point
145-151 ?C
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-DL-Phe-OH
CAS Number
4530-18-1
Purity
≥ 99% (HPLC)
Molecular Formula
C14H19NO4
Molecular Weight
265.31
MDL Number
MFCD00558969
PubChem ID
269698
Melting Point
145-151 ?C
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-DL-phenylalanine is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing chemists to selectively modify amino acids without affecting others, thus streamlining the creation of complex proteins.
  • Drug Development: It plays a role in the design of pharmaceuticals, particularly in creating compounds that can interact with specific biological targets, enhancing drug efficacy and specificity.
  • Biotechnology: In biotechnological applications, it is used in the production of recombinant proteins, aiding in the development of biologics that can treat various diseases.
  • Research in Neuroscience: The compound is utilized in studies related to neurotransmitter activity, helping researchers understand the role of amino acids in brain function and potential treatments for neurological disorders.
  • Cosmetic Formulations: Its properties make it suitable for use in cosmetic products, where it can enhance skin hydration and improve the texture of formulations.

Citations