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Catalog Number:
04660
CAS Number:
52551-07-2
L-tyrosine 4-nitroanilide
Purity:
≥ 99 % (HPLC)
Synonym(s):
L-Tyr-pNA
Documents
$65.40 /100 mg
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Informations sur le produit

L-Tyrosine 4-nitroanilide is a versatile compound widely recognized for its applications in biochemical research and analytical chemistry. This derivative of L-Tyrosine features a nitroaniline moiety, making it particularly useful as a chromogenic substrate in enzyme assays, especially for the detection of tyrosinase activity. Its unique structure allows for enhanced sensitivity and specificity in various assays, enabling researchers to obtain accurate results in studies related to enzymatic reactions and metabolic pathways.

In addition to its role in enzyme assays, L-Tyrosine 4-nitroanilide is also utilized in the synthesis of other bioactive compounds, contributing to the development of pharmaceuticals and agrochemicals. Its ability to undergo further chemical transformations makes it a valuable building block in organic synthesis. Researchers and industry professionals can leverage this compound's properties to streamline their workflows and enhance the efficiency of their experimental designs, ultimately leading to innovative solutions in their respective fields.

Numéro CAS 
52551-07-2
Formule moléculaire
C15H15N3O4
Poids moléculaire 
301.3
Point de fusion 
200-206 °C
Rotation optique 
[a] D 20 = +146,4 ± 4º (C = 1 dans 80 % d'AcOH)
Informations générales
Numéro CAS 
52551-07-2
Formule moléculaire
C15H15N3O4
Poids moléculaire 
301.3
Point de fusion 
200-206 °C
Rotation optique 
[a] D 20 = +146,4 ± 4º (C = 1 dans 80 % d'AcOH)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

L-Tyrosine 4-nitroanilide is widely utilized in research focused on:

  • Biochemical Assays: This compound serves as a substrate in enzyme assays, particularly for studying the activity of tyrosinase, which is crucial in melanin production and various biochemical pathways.
  • Colorimetric Detection: It is used in colorimetric assays to detect the presence of specific enzymes, providing a visual indication that is easy to interpret, making it valuable in laboratories.
  • Pharmaceutical Research: The compound plays a role in drug development, particularly in the synthesis of new pharmaceuticals targeting neurological disorders, due to its structural similarity to neurotransmitters.
  • Material Science: L-Tyrosine 4-nitroanilide is explored in the development of polymer materials that require specific thermal and mechanical properties, enhancing product performance.
  • Food Industry: It is applied in food technology for monitoring enzymatic reactions, ensuring quality control in food products that involve tyrosinase activity, such as in the browning of fruits.

Citations