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Catalog Number:
04367
CAS Number:
19746-40-8
Acetyl-L-leucine 4-nitroanilide
Purity:
≥ 95% (HPLC)
Synonym(s):
Ac-L-Leu-pNA
Documents
$120.00 /1G
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Product Information

Acetyl-L-leucine 4-nitroanilide is a versatile compound with significant applications in biochemical research and pharmaceutical development. This derivative of leucine features a unique nitrophenyl group, enhancing its utility in various assays and synthesis processes. Its structural properties make it an excellent candidate for studying enzyme kinetics and protein interactions, particularly in the context of metabolic pathways. Researchers have utilized Acetyl-L-leucine 4-nitroanilide in the development of novel therapeutic agents, leveraging its ability to modulate biological activity.

In addition to its research applications, this compound is also valuable in the synthesis of more complex molecules, serving as a building block in organic chemistry. Its stability and reactivity make it an attractive option for professionals looking to streamline their synthesis processes. With its combination of biochemical relevance and synthetic versatility, Acetyl-L-leucine 4-nitroanilide stands out as a crucial tool for researchers and industry professionals alike.

Synonyms
Ac-L-Leu-pNA
CAS Number
19746-40-8
Purity
≥ 95% (HPLC)
Molecular Formula
C14H19N3O4
Molecular Weight
293.32
MDL Number
MFCD00057927
PubChem ID
4313455
Appearance
Light yellow or off-white powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Ac-L-Leu-pNA
CAS Number
19746-40-8
Purity
≥ 95% (HPLC)
Molecular Formula
C14H19N3O4
Molecular Weight
293.32
MDL Number
MFCD00057927
PubChem ID
4313455
Appearance
Light yellow or off-white powder
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

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

  • Biochemical Research: This compound serves as a substrate in enzyme assays, allowing researchers to study enzyme kinetics and mechanisms, particularly in proteolytic enzymes.
  • Pharmaceutical Development: It is used in drug formulation studies, helping scientists evaluate the bioavailability and efficacy of new therapeutic agents.
  • Analytical Chemistry: The compound acts as a reagent in various analytical techniques, including chromatography and mass spectrometry, aiding in the identification and quantification of biomolecules.
  • Protein Synthesis Studies: Acetyl-L-leucine 4-nitroanilide is employed in studies related to protein synthesis, providing insights into amino acid incorporation and peptide bond formation.
  • Education and Training: It is often used in academic laboratories for teaching purposes, helping students understand organic synthesis and biochemical analysis techniques.

Citations