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Catalog Number:
06640
CAS Number:
71989-25-8
Chlorhydrate d'ester de L-leucine 4-nitrophényle
Purity:
≥ 98 % (HPLC)
Synonym(s):
L-Leu-ONp·HCl, Ester 4-nitrophénylique de l'acide ( S ) -2-amino-4-méthyl-pentanoïque
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Informations sur le produit

L-Leucine 4-nitrophenyl ester hydrochloride is a valuable compound in biochemical research and pharmaceutical applications. This derivative of the essential amino acid L-Leucine is recognized for its role in protein synthesis and metabolic regulation. Its unique structure enhances its solubility and bioavailability, making it an excellent choice for studies involving peptide synthesis and enzyme activity. Researchers often utilize this compound in the development of novel therapeutic agents, particularly in the fields of cancer research and metabolic disorders, where understanding amino acid interactions is crucial.

The compound's properties allow for its application in various assays and experimental setups, providing insights into protein interactions and cellular processes. Its ability to act as a substrate in enzymatic reactions makes it particularly useful for researchers exploring enzyme kinetics and mechanisms. Additionally, L-Leucine 4-nitrophenyl ester hydrochloride can serve as a building block in the synthesis of more complex molecules, offering significant advantages over similar compounds due to its stability and reactivity profile.

Numéro CAS 
71989-25-8
Formule moléculaire
C12H16N2O4 · HCl
Poids moléculaire 
288.68
Point de fusion 
> 176 °C (déc.)
Rotation optique 
[α] D 25 = +24 ± 1º (C=1 dans HCl 1N)
Informations générales
Numéro CAS 
71989-25-8
Formule moléculaire
C12H16N2O4 · HCl
Poids moléculaire 
288.68
Point de fusion 
> 176 °C (déc.)
Rotation optique 
[α] D 25 = +24 ± 1º (C=1 dans HCl 1N)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

L-Leucine 4-nitrophenyl ester hydrochloride is widely utilized in research focused on:

  • Biochemical Research: This compound serves as a substrate in enzyme assays, helping researchers study enzyme kinetics and mechanisms, particularly in protease activity.
  • Peptide Synthesis: It is used in the synthesis of peptides, allowing for the incorporation of L-leucine in various sequences, which is crucial for developing biologically active compounds.
  • Drug Development: The ester form enhances solubility and bioavailability of L-leucine, making it a valuable candidate in formulating new pharmaceuticals aimed at muscle recovery and metabolic health.
  • Analytical Chemistry: This compound is employed in chromatographic techniques for the separation and identification of amino acids, providing a reliable method for quality control in food and pharmaceutical industries.
  • Nutrition Science: It is investigated for its role in protein synthesis and muscle growth, offering insights into dietary supplements that can enhance athletic performance and recovery.

Citations