H-DL-Phe-OEt.HCl

97%

Reagent Code: #50219
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CAS Number 19881-53-9

science Other reagents with same CAS 19881-53-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.70 g/mol
Formula C₁₁H₁₆ClNO₂
badge Registry Numbers
MDL Number MFCD02063363
thermostat Physical Properties
Boiling Point 281.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used in peptide synthesis as a building block for creating complex peptides and proteins. It serves as a protected form of phenylalanine, ensuring stability during chemical reactions. Commonly applied in pharmaceutical research for developing peptide-based drugs. Also utilized in biochemical studies to investigate enzyme mechanisms and protein interactions. Its ester group allows for selective deprotection, enabling precise control in synthetic processes.

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Test Parameter Specification
Appearance White to Off-White Powder
Purity (%) 96.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,854.00
inventory 25g
10-20 days ฿3,411.00
inventory 10g
10-20 days ฿2,655.00

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H-DL-Phe-OEt.HCl
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Used in peptide synthesis as a building block for creating complex peptides and proteins. It serves as a protected form of phenylalanine, ensuring stability during chemical reactions. Commonly applied in pharmaceutical research for developing peptide-based drugs. Also utilized in biochemical studies to investigate enzyme mechanisms and protein interactions. Its ester group allows for selective deprotection, enabling precise control in synthetic processes.

Used in peptide synthesis as a building block for creating complex peptides and proteins. It serves as a protected form of phenylalanine, ensuring stability during chemical reactions. Commonly applied in pharmaceutical research for developing peptide-based drugs. Also utilized in biochemical studies to investigate enzyme mechanisms and protein interactions. Its ester group allows for selective deprotection, enabling precise control in synthetic processes.

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