(S)-2-Amino-3-(4-sulfophenyl)propanoic acid

≥97%

Reagent Code: #47808
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CAS Number 34023-49-9

science Other reagents with same CAS 34023-49-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.25 g/mol
Formula C₉H₁₁NO₅S
badge Registry Numbers
MDL Number MFCD00270366
inventory_2 Storage & Handling
Density 1.53g/cm3
Storage Room temperature, airtight, dry

description Product Description

(S)-2-Amino-3-(4-sulfophenyl)propanoic acid is primarily utilized in biochemical research as a specialized amino acid derivative. It serves as a key intermediate in the synthesis of peptides and proteins, particularly in studies focusing on enzyme activity and protein structure. Its sulfophenyl group makes it useful for investigating interactions with enzymes that recognize or bind to sulfated substrates. Additionally, it is employed in the development of fluorescent probes and markers for tracking biological processes, as the sulfonate group enhances solubility and stability in aqueous environments. This compound is also explored in drug discovery for designing molecules that target specific protein receptors or enzymes involved in disease pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,600.00
inventory 250mg
10-20 days ฿36,800.00
inventory 1g
10-20 days ฿88,000.00

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(S)-2-Amino-3-(4-sulfophenyl)propanoic acid
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(S)-2-Amino-3-(4-sulfophenyl)propanoic acid is primarily utilized in biochemical research as a specialized amino acid derivative. It serves as a key intermediate in the synthesis of peptides and proteins, particularly in studies focusing on enzyme activity and protein structure. Its sulfophenyl group makes it useful for investigating interactions with enzymes that recognize or bind to sulfated substrates. Additionally, it is employed in the development of fluorescent probes and markers for tracking biolo

(S)-2-Amino-3-(4-sulfophenyl)propanoic acid is primarily utilized in biochemical research as a specialized amino acid derivative. It serves as a key intermediate in the synthesis of peptides and proteins, particularly in studies focusing on enzyme activity and protein structure. Its sulfophenyl group makes it useful for investigating interactions with enzymes that recognize or bind to sulfated substrates. Additionally, it is employed in the development of fluorescent probes and markers for tracking biological processes, as the sulfonate group enhances solubility and stability in aqueous environments. This compound is also explored in drug discovery for designing molecules that target specific protein receptors or enzymes involved in disease pathways.

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