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Catalog Number:
00153
CAS Number:
122864-94-2, 7300-59-6
L-Glutamic acid 5-(4-nitroanilide) monohydrate
Synonym(s):
L-g-Glutamyl-p-nitroanilide monohydrate
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Product Information

L-Glutamic acid 5-(4-nitroanilide) monohydrate is a specialized compound that plays a significant role in various biochemical applications. This derivative of L-Glutamic acid is recognized for its utility in the synthesis of peptide-based drugs and as a reagent in analytical chemistry. Its unique structure, featuring a nitroanilide group, enhances its reactivity, making it an excellent candidate for use in enzyme assays and as a substrate in biochemical research. Researchers appreciate its ability to facilitate studies on neurotransmitter activity, particularly in the context of neurobiology, where it can help elucidate the mechanisms of synaptic transmission.

In addition to its applications in research, L-Glutamic acid 5-(4-nitroanilide) monohydrate is also valuable in the development of diagnostic tools, particularly in assays that require specific interactions with amino acids. Its stability and solubility in aqueous solutions further enhance its practicality for laboratory use. This compound stands out due to its dual functionality, serving both as a building block in organic synthesis and as a critical component in various analytical methods, making it an essential resource for professionals in the fields of biochemistry and pharmaceuticals.

Synonyms
L-g-Glutamyl-p-nitroanilide monohydrate
CAS Number
122864-94-2, 7300-59-6
Molecular Formula
C11H13N3O5·H2O
Molecular Weight
285.3
MDL Number
MFCD00066286
Melting Point
183-187 °C
Appearance
Cream colored solid
Conditions
Store at 0-8 °C
General Information
Synonyms
L-g-Glutamyl-p-nitroanilide monohydrate
CAS Number
122864-94-2, 7300-59-6
Molecular Formula
C11H13N3O5·H2O
Molecular Weight
285.3
MDL Number
MFCD00066286
Melting Point
183-187 °C
Appearance
Cream colored solid
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

L-Glutamic acid 5-(4-nitroanilide) monohydrate is widely utilized in research focused on:

  • Biochemical assays: This compound serves as a substrate in enzyme assays, particularly for glutamate dehydrogenase, allowing researchers to study enzyme kinetics and metabolic pathways.
  • Pharmaceutical development: It is used in drug formulation and testing, particularly in the development of neuroprotective agents, due to its role in neurotransmitter signaling.
  • Food industry: As a flavor enhancer, it can improve the taste profile of various food products, making it valuable for food scientists and manufacturers.
  • Diagnostics: The compound is employed in diagnostic tests for certain diseases, helping healthcare professionals identify conditions related to amino acid metabolism.
  • Research on neurological disorders: It is utilized in studies investigating the role of glutamate in neurodegenerative diseases, providing insights that could lead to new therapeutic strategies.

Citations