(S)-2-Amino-3-guanidinopropanoic acid dihydrochloride

95%

Reagent Code: #38286
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CAS Number 2216751-08-3

science Other reagents with same CAS 2216751-08-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.07 g/mol
Formula C₄H₁₂Cl₂N₄O₂
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

(S)-2-Amino-3-guanidinopropanoic acid dihydrochloride is primarily used in biochemical research and pharmaceutical development. It serves as a precursor or intermediate in the synthesis of more complex organic compounds, particularly those with potential therapeutic applications. Its structure, featuring both amino and guanidinium groups, makes it valuable in studying enzyme mechanisms and protein interactions, especially in the context of arginine metabolism. Additionally, it is employed in the development of peptide-based drugs, where its functional groups can enhance binding affinity or stability. In laboratory settings, it is also utilized as a reagent for modifying or labeling biomolecules to investigate biological processes.

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Test Parameter Specification
Appearance White Powder
Purity (Titration By AgNO3) >=94.5%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,456.00
inventory 5g
10-20 days ฿18,090.00
inventory 1g
10-20 days ฿6,912.00

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(S)-2-Amino-3-guanidinopropanoic acid dihydrochloride
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(S)-2-Amino-3-guanidinopropanoic acid dihydrochloride is primarily used in biochemical research and pharmaceutical development. It serves as a precursor or intermediate in the synthesis of more complex organic compounds, particularly those with potential therapeutic applications. Its structure, featuring both amino and guanidinium groups, makes it valuable in studying enzyme mechanisms and protein interactions, especially in the context of arginine metabolism. Additionally, it is employed in the development of peptide-based drugs, where its functional groups can enhance binding affinity or stability. In laboratory settings, it is also utilized as a reagent for modifying or labeling biomolecules to investigate biological processes.
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