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Catalog Number:
16810
CAS Number:
1217849-53-0
D-2,4-Dinitrophenylalanine
Synonym(s):
D-Phe(2,4-DiNO2)-OH, (R-2-Amino-3-(2,4-dinitrophenyl)propionic acid, H-D-Phe(2,4-DiNO2)-OH
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$336.70 /1G
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Product Information

D-2,4-Dinitrophenylalanine is a specialized amino acid derivative that plays a significant role in biochemical research and applications. This compound is recognized for its unique dinitrophenyl group, which enhances its reactivity and makes it a valuable tool in the study of protein interactions and enzyme mechanisms. Researchers often utilize D-2,4-Dinitrophenylalanine in the synthesis of peptide-based probes and as a labeling agent in various assays, enabling the investigation of protein structure and function. Its ability to form stable conjugates with proteins allows for the precise tracking of biomolecular interactions, making it an essential component in drug discovery and development.

In addition to its applications in research, D-2,4-Dinitrophenylalanine is also relevant in the field of immunology, where it can be used to create immunogenic conjugates for vaccine development. Its distinctive properties provide a competitive advantage over similar compounds, as it offers enhanced specificity and sensitivity in detection methods. This versatility makes D-2,4-Dinitrophenylalanine an indispensable asset for researchers and industry professionals looking to advance their work in biochemistry and molecular biology.

Synonyms
D-Phe(2,4-DiNO2)-OH, (R-2-Amino-3-(2,4-dinitrophenyl)propionic acid, H-D-Phe(2,4-DiNO2)-OH
CAS Number
1217849-53-0
Molecular Formula
C9H9N3O6
Molecular Weight
255.18
MDL Number
MFCD08061613
PubChem ID
9837950
Conditions
Store at 0-8°C
General Information
Synonyms
D-Phe(2,4-DiNO2)-OH, (R-2-Amino-3-(2,4-dinitrophenyl)propionic acid, H-D-Phe(2,4-DiNO2)-OH
CAS Number
1217849-53-0
Molecular Formula
C9H9N3O6
Molecular Weight
255.18
MDL Number
MFCD08061613
PubChem ID
9837950
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

D-2,4-Dinitrophenylalanine is widely utilized in research focused on:

  • Protein Engineering: This compound serves as a useful tool for studying protein folding and stability, allowing researchers to modify proteins and analyze their structural changes.
  • Biochemical Assays: It is employed in various assays to detect and quantify amino acids, enhancing the accuracy of biochemical analyses in laboratories.
  • Drug Development: The compound is used in the design of new pharmaceuticals, particularly in understanding how modifications to amino acids can affect drug efficacy and safety.
  • Environmental Studies: Researchers utilize it to investigate the effects of pollutants on biological systems, contributing to environmental monitoring and protection efforts.
  • Education and Training: It is often included in academic curricula for chemistry and biochemistry, providing students with hands-on experience in organic synthesis and analytical techniques.

Citations