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Catalog Number:
42980
CAS Number:
4333-19-1
Phenylthiohydantoin-alanine
Purity:
≥ 98% (HPLC)
Synonym(s):
5-Methyl-3-phenyl-2-thiohydantoin, PTH-alanine
Hazmat
Documents
$70.41 /100MG
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Product Information

Phenylthiohydantoin-alanine is a versatile compound widely recognized for its applications in biochemical research and pharmaceutical development. This compound serves as a valuable reagent in the synthesis of amino acids and peptides, particularly in the context of protein sequencing and analysis. Its unique structure, featuring a phenylthio group, enhances its reactivity and selectivity, making it an ideal choice for researchers looking to explore complex biochemical pathways.

In addition to its utility in synthetic chemistry, Phenylthiohydantoin-alanine is instrumental in the development of diagnostic tools and therapeutic agents. Its ability to form stable derivatives with amino acids allows for precise identification and quantification in various biological samples. Researchers in the fields of biochemistry and molecular biology will find this compound particularly beneficial for its role in elucidating protein structures and functions, paving the way for advancements in drug discovery and development.

Synonyms
5-Methyl-3-phenyl-2-thiohydantoin, PTH-alanine
CAS Number
4333-19-1
Purity
≥ 98% (HPLC)
Molecular Formula
C10H10N2OS
Molecular Weight
206.26
MDL Number
MFCD06858229
PubChem ID
2872314
Melting Point
184 - 188 °C
Appearance
White to orange to green crystalline powder
Conditions
Store at RT
General Information
Synonyms
5-Methyl-3-phenyl-2-thiohydantoin, PTH-alanine
CAS Number
4333-19-1
Purity
≥ 98% (HPLC)
Molecular Formula
C10H10N2OS
Molecular Weight
206.26
MDL Number
MFCD06858229
PubChem ID
2872314
Melting Point
184 - 188 °C
Appearance
White to orange to green crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Phenylthiohydantoin-alanine is widely utilized in research focused on:

  • Protein Sequencing: This compound is employed in Edman degradation, a method for sequencing amino acids in proteins, allowing researchers to determine the structure and function of proteins accurately.
  • Peptide Synthesis: It serves as a key reagent in synthesizing peptides, which are essential for various biological applications, including drug development and vaccine formulation.
  • Analytical Chemistry: Used in chromatography techniques, it helps in the separation and analysis of complex mixtures, making it invaluable for quality control in pharmaceuticals.
  • Biochemical Research: The compound is instrumental in studying enzyme activity and interactions, aiding researchers in understanding metabolic pathways and disease mechanisms.
  • Diagnostic Applications: It has potential uses in developing diagnostic tests for various diseases, leveraging its ability to interact with specific biomolecules.

Citations