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Catalog Number:
06303
CAS Number:
214750-67-1
Nα-Boc-Nβ-2,4-dinitrophenyl-L-2,3-diaminopropionic acid
Purity:
99%
Synonym(s):
Boc-L-Dap(Dnp)-OH
Documents
$240.00 /1G
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Product Information

Na-Boc-Nb-2,4-dinitrophenyl-L-2,3-diaminopropionic acid is a specialized compound recognized for its unique properties and applications in the field of biochemistry and pharmaceuticals. This compound features a dinitrophenyl group, which enhances its reactivity and makes it an excellent candidate for use in the synthesis of peptide-based therapeutics. Its Boc (tert-butyloxycarbonyl) protecting group allows for selective deprotection, facilitating the incorporation of this compound into complex molecular architectures.

Researchers and industry professionals can leverage Na-Boc-Nb-2,4-dinitrophenyl-L-2,3-diaminopropionic acid in drug development, particularly in the design of targeted therapies and diagnostic agents. Its ability to form stable conjugates with biomolecules opens avenues for innovative applications in targeted drug delivery systems. Additionally, the compound's properties make it suitable for use in various analytical techniques, including chromatography and mass spectrometry, enhancing its utility in both research and industrial settings.

Synonyms
Boc-L-Dap(Dnp)-OH
CAS Number
214750-67-1
Purity
99%
Molecular Formula
C14H18N4O8
Molecular Weight
370.45
MDL Number
MFCD00798630
PubChem ID
74765380
Melting Point
125- 128 °C (dec.)
Appearance
Off-white to yellow powder
Optical Rotation
[a]20D = 46 ± 2 º (C=1.316 in MeOH)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-L-Dap(Dnp)-OH
CAS Number
214750-67-1
Purity
99%
Molecular Formula
C14H18N4O8
Molecular Weight
370.45
MDL Number
MFCD00798630
PubChem ID
74765380
Melting Point
125- 128 °C (dec.)
Appearance
Off-white to yellow powder
Optical Rotation
[a]20D = 46 ± 2 º (C=1.316 in MeOH)
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

Na-Boc-Nb-2,4-dinitrophenyl-L-2,3-diaminopropionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions without interfering with other functional groups.
  • Drug Development: It plays a role in the design of novel pharmaceuticals, particularly in creating compounds that target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: Researchers use it for attaching biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems.
  • Analytical Chemistry: The compound is employed in the development of assays and sensors, providing a means to detect specific analytes with high sensitivity.
  • Material Science: It is utilized in the formulation of advanced materials, contributing to the development of polymers with unique properties for various applications.

Citations