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Catalog Number:
16813
CAS Number:
1176509-56-0
Boc-L-2,4-dinitrophénylalanine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-L-Phe(2,4-DiNO2)-OH, ( Acide S -Boc-2-amino-3-(2,4-dinitrophényl)propionique, Boc-Phe(2,4-DiNO2)-OH
Documents
$106.96 /100 mg
Taille
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Product Information

Boc-L-2,4-dinitrophenylalanine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and bioconjugation applications. This compound, known for its unique dinitrophenyl group, enhances the reactivity of peptides, making it an invaluable tool in the development of targeted therapeutics and diagnostic agents. Its protective Boc (tert-butyloxycarbonyl) group allows for selective deprotection, facilitating the incorporation of this amino acid into complex peptide sequences. Researchers in the fields of medicinal chemistry and biochemistry can leverage Boc-L-2,4-dinitrophenylalanine to create novel compounds with improved efficacy and specificity.

This compound is particularly advantageous in the synthesis of peptide-based drugs, where the dinitrophenyl moiety can serve as a useful chromophore for analytical applications, such as UV-Vis spectroscopy. Additionally, its ability to form stable conjugates with biomolecules opens avenues for the development of innovative drug delivery systems. With its unique properties and practical applications, Boc-L-2,4-dinitrophenylalanine stands out as a key reagent for researchers aiming to advance their work in peptide chemistry and related fields.

Synonyms
Boc-L-Phe(2,4-DiNO2)-OH, ( Acide S -Boc-2-amino-3-(2,4-dinitrophényl)propionique, Boc-Phe(2,4-DiNO2)-OH
CAS Number
1176509-56-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C14H17N3O8
Molecular Weight
355.3
MDL Number
MFCD08061620
PubChem ID
53398473
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = + 24 ± 2 ° (C=1, dans MeOH)
Conditions
Conserver à 0-8°C
General Information
Synonyms
Boc-L-Phe(2,4-DiNO2)-OH, ( Acide S -Boc-2-amino-3-(2,4-dinitrophényl)propionique, Boc-Phe(2,4-DiNO2)-OH
CAS Number
1176509-56-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C14H17N3O8
Molecular Weight
355.3
MDL Number
MFCD08061620
PubChem ID
53398473
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = + 24 ± 2 ° (C=1, dans MeOH)
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-L-2,4-dinitrophenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a building block in the synthesis of peptides, allowing researchers to create complex structures for studying protein interactions and functions.
  • Drug Development: Its unique properties make it valuable in the pharmaceutical industry for developing new drugs, particularly those targeting specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation techniques to attach biomolecules to surfaces or other molecules, enhancing the specificity and efficacy of therapeutic agents.
  • Analytical Chemistry: It is employed in analytical methods to detect and quantify amino acids and peptides, aiding researchers in quality control and characterization of biological samples.
  • Immunology Research: The compound is utilized in immunological studies to create antigens that can elicit specific immune responses, facilitating vaccine development and immune profiling.

Citations