Fmoc-D-Alanine
98%
- Product Code: 50824
Alias:
Fmoc-D-alanine ; N-fluorenylmethoxycarbonyl-D-alanine
CAS:
79990-15-1
| Molecular Weight: | 311.332 g./mol | Molecular Formula: | C₁₈H₁₇NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00062960 | |
| Melting Point: | 151-155 ℃ | Boiling Point: | 544.1ºC at 760 mmHg |
| Density: | 1.282 g/cm3 | Storage Condition: | 2~8℃ |
Product Description:
Fmoc-D-Alanine is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a building block for introducing D-alanine residues into peptide chains, which is crucial for creating peptides with specific stereochemistry. The Fmoc (fluorenylmethyloxycarbonyl) protecting group ensures selective deprotection during synthesis, allowing for precise control over the assembly of peptide sequences. This compound is essential in the development of peptidomimetics, bioactive peptides, and pharmaceuticals, where the incorporation of D-amino acids can enhance stability, bioavailability, and resistance to enzymatic degradation. Additionally, it is employed in research to study the effects of D-amino acids on peptide structure and function, contributing to advancements in drug discovery and biochemical studies.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 151 155? |
| PURITYHPLC | 98 100% |
| PURITYNEUTRALIZATION TITRATION | 98 100% |
| SPECIFIC ROTATION A20DC1DMF | 17-21 |
| WATER BY KARL FISCHER | 0 7% |
| APPEARANCE | WHITE TO LIGHT YELLOW POWDER |
| INFRARED SPECTROMETRY | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | $14.06 |
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| 25.000 | 10-20 days | $37.17 |
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| 100.000 | 10-20 days | $141.14 |
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| 500.000 | 10-20 days | $647.41 |
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Fmoc-D-Alanine
Fmoc-D-Alanine is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a building block for introducing D-alanine residues into peptide chains, which is crucial for creating peptides with specific stereochemistry. The Fmoc (fluorenylmethyloxycarbonyl) protecting group ensures selective deprotection during synthesis, allowing for precise control over the assembly of peptide sequences. This compound is essential in the development of peptidomimetics, bioactive peptides, and pharmaceuticals, where the incorporation of D-amino acids can enhance stability, bioavailability, and resistance to enzymatic degradation. Additionally, it is employed in research to study the effects of D-amino acids on peptide structure and function, contributing to advancements in drug discovery and biochemical studies.
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