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Catalog Number:
41757
CAS Number:
29635-94-7
Phenylthiohydantoin-(Ne-phenylthiocarbamyl)-lysine
Purity:
≥ 98% (HPLC)
Synonym(s):
PTH-(Ne-PTC)-lysine
Documents
$25.00 /100MG
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Product Information

Phenylthiohydantoin-(N?-phenylthiocarbamyl)-lysine is a versatile compound with significant applications in biochemical research and pharmaceutical development. This compound is recognized for its role in the synthesis of peptide derivatives and as a reagent in the identification of amino acids. Its unique structure allows it to participate in various chemical reactions, making it an essential tool for researchers working in the fields of organic chemistry and biochemistry.

In practical applications, Phenylthiohydantoin is often utilized in the analysis of protein sequences and in the development of new therapeutic agents. Its ability to form stable complexes with amino acids enhances its utility in chromatographic techniques, providing researchers with reliable results. Additionally, its compatibility with various analytical methods makes it a preferred choice for laboratories focused on peptide synthesis and characterization. By incorporating this compound into their workflows, professionals can streamline their research processes and achieve more accurate outcomes.

Synonyms
PTH-(Ne-PTC)-lysine
CAS Number
29635-94-7
Purity
≥ 98% (HPLC)
Molecular Formula
C20H22N4OS2
Molecular Weight
398.54
MDL Number
MFCD00151476
PubChem ID
3034586
Melting Point
162 - 166 °C
Appearance
White to light yellow powder to crystal
Conditions
Store at RT
General Information
Synonyms
PTH-(Ne-PTC)-lysine
CAS Number
29635-94-7
Purity
≥ 98% (HPLC)
Molecular Formula
C20H22N4OS2
Molecular Weight
398.54
MDL Number
MFCD00151476
PubChem ID
3034586
Melting Point
162 - 166 °C
Appearance
White to light yellow powder to crystal
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-(N?-phenylthiocarbamyl)-lysine is widely utilized in research focused on:

  • Protein Sequencing: This compound is commonly used in the Edman degradation method, which allows researchers to determine the amino acid sequence of proteins. Its ability to selectively react with the amino terminal of peptides makes it invaluable in proteomics.
  • Biochemical Assays: It serves as a reagent in various biochemical assays, helping to identify and quantify proteins in complex mixtures. This is particularly useful in drug development and diagnostics.
  • Pharmaceutical Development: The compound is explored in the synthesis of novel pharmaceuticals, particularly those targeting specific proteins. Its unique structure can lead to the development of drugs with improved efficacy and reduced side effects.
  • Research in Enzyme Activity: It is used in studies investigating enzyme kinetics and mechanisms, providing insights into how enzymes interact with substrates, which is crucial for understanding metabolic pathways.
  • Analytical Chemistry: The compound aids in the development of analytical methods for detecting and quantifying amino acids and peptides, enhancing the accuracy of research in food science and nutrition.

Citations