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Catalog Number:
41751
CAS Number:
4332-97-2
Phenylthiohydantoin-phenylalanine
Purity:
≥ 98% (HPLC)
Synonym(s):
5-Benzyl-3-phenyl-2-thiohydantoin, PTH-phenylalanine
Documents
$45.37 /100MG
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Product Information

Phenylthiohydantoin-phenylalanine is a versatile compound known for its unique properties and applications in biochemical research and pharmaceutical development. This compound, characterized by its imidazolidinone structure, serves as a valuable tool in peptide synthesis and amino acid analysis. Its ability to form stable derivatives makes it particularly useful for researchers engaged in the study of protein structures and functions.

In practical applications, Phenylthiohydantoin-phenylalanine is commonly utilized in the Edman degradation process, a method for sequencing amino acids in proteins. This compound enhances the efficiency of the process, allowing for accurate identification of amino acid sequences. Additionally, its role in the synthesis of peptide derivatives opens avenues for drug development, particularly in creating targeted therapies. Researchers and industry professionals can leverage this compound's unique properties to advance their work in biochemistry and pharmacology, making it an essential addition to any laboratory focused on protein chemistry and related fields.

Synonyms
5-Benzyl-3-phenyl-2-thiohydantoin, PTH-phenylalanine
CAS Number
4332-97-2
Purity
≥ 98% (HPLC)
Molecular Formula
C16H14N2OS
Molecular Weight
282.36
MDL Number
MFCD01076623
PubChem ID
2871911
Melting Point
187 - 191 °C
Appearance
White to off-white powder
Conditions
Store at RT
General Information
Synonyms
5-Benzyl-3-phenyl-2-thiohydantoin, PTH-phenylalanine
CAS Number
4332-97-2
Purity
≥ 98% (HPLC)
Molecular Formula
C16H14N2OS
Molecular Weight
282.36
MDL Number
MFCD01076623
PubChem ID
2871911
Melting Point
187 - 191 °C
Appearance
White to off-white powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Phenylthiohydantoin-phenylalanine is widely utilized in research focused on:

  • Protein Sequencing: This compound is used in the Edman degradation method, a technique for sequencing amino acids in proteins. It helps researchers identify the primary structure of proteins, which is crucial for understanding their function.
  • Peptide Synthesis: It serves as a building block in the synthesis of peptides. This application is particularly valuable in pharmaceuticals, where custom peptides are needed for drug development.
  • Biochemical Assays: The compound is employed in various biochemical assays to study enzyme activity and interactions, aiding in drug discovery and development processes.
  • Research in Neurobiology: Its derivatives can be used to explore neurobiological pathways, contributing to the understanding of neurological disorders and potential therapeutic targets.
  • Analytical Chemistry: This chemical plays a role in analytical techniques such as chromatography, helping to separate and identify complex mixtures in various samples, including biological fluids.

Citations