L-Azetidine-2-carboxylic acid

99%

Reagent Code: #110574
label
Alias 2-Azetidinecarboxylic acid, (S)-azetidine-2-carboxylic acid
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CAS Number 2133-34-8

science Other reagents with same CAS 2133-34-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 101.1 g/mol
Formula C₄H₇NO₂
badge Registry Numbers
EC Number 218-362-5
MDL Number MFCD00005166
thermostat Physical Properties
Melting Point ~215 °C (dec.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

L-Azetidine-2-carboxylic acid is primarily utilized in biochemical research as a proline analog. It is incorporated into proteins in place of proline, which allows scientists to study protein structure and function by observing the effects of this substitution. This compound is particularly valuable in understanding the role of proline in protein folding and stability. Additionally, it is used in the synthesis of various peptides and peptidomimetics, aiding in the development of new pharmaceuticals. Its ability to mimic proline makes it a useful tool in probing enzymatic mechanisms and interactions within biological systems.

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Test Parameter Specification
Appearance white to faint yellow, faint beige, and faint brown solid
Purity (%) 98.5
Melting Point (°C) 205-220
Specific Rotation [A]20/D (C=4, H2O) -125 to -120

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,500.00
inventory 50mg
10-20 days ฿590.00
inventory 250mg
10-20 days ฿1,750.00
inventory 5g
10-20 days ฿13,500.00

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L-Azetidine-2-carboxylic acid
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L-Azetidine-2-carboxylic acid is primarily utilized in biochemical research as a proline analog. It is incorporated into proteins in place of proline, which allows scientists to study protein structure and function by observing the effects of this substitution. This compound is particularly valuable in understanding the role of proline in protein folding and stability. Additionally, it is used in the synthesis of various peptides and peptidomimetics, aiding in the development of new pharmaceuticals. Its ability to mimic proline makes it a useful tool in probing enzymatic mechanisms and interactions within biological systems.
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