H-3-D-Pal-OH.HCl

≥95%

Reagent Code: #44291
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CAS Number 350228-35-2

science Other reagents with same CAS 350228-35-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.64 g/mol
Formula C₈H₁₁ClN₂O₂
badge Registry Numbers
MDL Number MFCD03095567
inventory_2 Storage & Handling
Storage room temperature, stored under inert gas

description Product Description

This compound is primarily utilized in peptide synthesis as a building block for creating specific peptide sequences. It serves as a form of the unnatural amino acid D-Pal (3-(3-pyridyl)-D-alanine), enabling controlled reactions during peptide chain assembly. Its application is significant in the development of pharmaceuticals, particularly in the design of peptide-based drugs, which require precise stereochemistry for biological activity. Additionally, it is used in research to study enzyme-substrate interactions and to explore the role of D-amino acids in biological systems. Its hydrochloride form ensures stability and solubility, making it suitable for various experimental and industrial processes.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,040.00
inventory 10g
10-20 days ฿14,418.00
inventory 5g
10-20 days ฿10,089.00

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H-3-D-Pal-OH.HCl
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This compound is primarily utilized in peptide synthesis as a building block for creating specific peptide sequences. It serves as a form of the unnatural amino acid D-Pal (3-(3-pyridyl)-D-alanine), enabling controlled reactions during peptide chain assembly. Its application is significant in the development of pharmaceuticals, particularly in the design of peptide-based drugs, which require precise stereochemistry for biological activity. Additionally, it is used in research to study enzyme-substrate in

This compound is primarily utilized in peptide synthesis as a building block for creating specific peptide sequences. It serves as a form of the unnatural amino acid D-Pal (3-(3-pyridyl)-D-alanine), enabling controlled reactions during peptide chain assembly. Its application is significant in the development of pharmaceuticals, particularly in the design of peptide-based drugs, which require precise stereochemistry for biological activity. Additionally, it is used in research to study enzyme-substrate interactions and to explore the role of D-amino acids in biological systems. Its hydrochloride form ensures stability and solubility, making it suitable for various experimental and industrial processes.

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