Phenylthiohydantoin-valine

≥98%

Reagent Code: #123141
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CAS Number 4333-20-4

science Other reagents with same CAS 4333-20-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.32 g/mol
Formula C₁₂H₁₄N₂OS
badge Registry Numbers
MDL Number MFCD06858300
thermostat Physical Properties
Melting Point 207-210°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Phenylthiohydantoin-valine is primarily used in the field of protein sequencing and peptide analysis. It plays a critical role in the Edman degradation process, a method for determining the amino acid sequence of proteins. Specifically, it is formed as a derivative during the cleavage step of the Edman degradation, allowing researchers to identify the N-terminal amino acid of a peptide or protein. This compound is essential for analyzing protein structures, understanding their functions, and studying post-translational modifications. Its application is particularly valuable in biochemistry, molecular biology, and proteomics research, aiding in the development of diagnostic tools and therapeutic agents.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿864.00
inventory 1g
10-20 days ฿6,300.00
inventory 250mg
10-20 days ฿2,385.00

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Phenylthiohydantoin-valine
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Phenylthiohydantoin-valine is primarily used in the field of protein sequencing and peptide analysis. It plays a critical role in the Edman degradation process, a method for determining the amino acid sequence of proteins. Specifically, it is formed as a derivative during the cleavage step of the Edman degradation, allowing researchers to identify the N-terminal amino acid of a peptide or protein. This compound is essential for analyzing protein structures, understanding their functions, and studying pos

Phenylthiohydantoin-valine is primarily used in the field of protein sequencing and peptide analysis. It plays a critical role in the Edman degradation process, a method for determining the amino acid sequence of proteins. Specifically, it is formed as a derivative during the cleavage step of the Edman degradation, allowing researchers to identify the N-terminal amino acid of a peptide or protein. This compound is essential for analyzing protein structures, understanding their functions, and studying post-translational modifications. Its application is particularly valuable in biochemistry, molecular biology, and proteomics research, aiding in the development of diagnostic tools and therapeutic agents.

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