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Catalog Number:
16811
CAS Number:
49607-21-8
L-2,4-Dinitrophenylalanine
Purity:
≥ 99% (HPLC)
Synonym(s):
L-Phe(2,4-DiNO2)-OH, (S)-2-Amino-3-(2,4-dinitrophenyl)propionic acid, H-Phe(2,4-DiNO2)-OH
Documents
$62.29 /25MG
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Product Information

L-2,4-Dinitrophenylalanine is a specialized amino acid derivative known for its unique properties and applications in biochemical research. This compound, characterized by the presence of two nitro groups on the phenyl ring, serves as a valuable tool in the study of protein structure and function. Its ability to form stable conjugates with proteins makes it particularly useful in the development of antibodies and in the study of enzyme kinetics. Researchers often utilize L-2,4-Dinitrophenylalanine in the synthesis of labeled peptides, which can be employed in various assays to track biological processes or interactions.

In addition to its applications in research, L-2,4-Dinitrophenylalanine has potential uses in the pharmaceutical industry, particularly in drug design and development. Its unique structure allows for the exploration of new therapeutic pathways and the creation of innovative drug candidates. The compound's reactivity and specificity can lead to advancements in targeted therapies, making it an essential component for researchers and professionals aiming to push the boundaries of biochemical science.

Synonyms
L-Phe(2,4-DiNO2)-OH, (S)-2-Amino-3-(2,4-dinitrophenyl)propionic acid, H-Phe(2,4-DiNO2)-OH
CAS Number
49607-21-8
Purity
≥ 99% (HPLC)
Molecular Formula
C9H9N3O6
Molecular Weight
255.18
MDL Number
MFCD08061615
PubChem ID
9837950
Melting Point
> 300 °C
Appearance
Yellowish to brown powder
Optical Rotation
[a]D25 = 38 ± 1 º (C=1 in 1N HCl)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
L-Phe(2,4-DiNO2)-OH, (S)-2-Amino-3-(2,4-dinitrophenyl)propionic acid, H-Phe(2,4-DiNO2)-OH
CAS Number
49607-21-8
Purity
≥ 99% (HPLC)
Molecular Formula
C9H9N3O6
Molecular Weight
255.18
MDL Number
MFCD08061615
PubChem ID
9837950
Melting Point
> 300 °C
Appearance
Yellowish to brown powder
Optical Rotation
[a]D25 = 38 ± 1 º (C=1 in 1N HCl)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Protein Engineering: This compound serves as a valuable tool for studying protein structure and function, allowing researchers to introduce specific modifications to amino acids in proteins, which can lead to insights into enzyme activity and stability.
  • Antibody Production: It is used as a hapten in the development of antibodies, enabling scientists to create targeted immunoassays for detecting specific proteins, which is crucial in diagnostics and therapeutic applications.
  • Biochemical Assays: The compound is employed in various biochemical assays to measure enzyme activity, particularly in studies involving oxidative stress and metabolic pathways, providing critical data for understanding cellular processes.
  • Drug Development: In pharmaceutical research, it aids in the identification of potential drug candidates by evaluating their interactions with biological targets, streamlining the drug discovery process.
  • Educational Purposes: It is often used in academic settings for teaching purposes, helping students understand complex biochemical concepts through hands-on experiments and demonstrations.

Citations