L-Azetidine-2-carboxylic acid
99%
- Product Code: 110574
Alias:
2-Azetidinecarboxylic acid, (S)-azetidine-2-carboxylic acid
CAS:
2133-34-8
| Molecular Weight: | 101.1 g./mol | Molecular Formula: | C₄H₇NO₂ |
|---|---|---|---|
| EC Number: | 218-362-5 | MDL Number: | MFCD00005166 |
| Melting Point: | ~215 °C (dec.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
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.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Faint Yellow And Faint Beige And Faint Brown Solid |
| Purity (%) | 98.5 |
| Melting Point (Degree Celsius) | 205-220 |
| Specific Rotation [A]20/D(C=4, H2O) | -125--120 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $23.20 |
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| 0.250 | 10-20 days | $68.82 |
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| 1.000 | 10-20 days | $137.64 |
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| 5.000 | 10-20 days | $530.90 |
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L-Azetidine-2-carboxylic acid
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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