Fmoc-D-Abu-OH
97%
- Product Code: 67436
CAS:
170642-27-0
| Molecular Weight: | 325.36 g./mol | Molecular Formula: | C₁₉H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00270336 | |
| Melting Point: | Boiling Point: | 550.7°C | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
Fmoc-D-Abu-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality during the synthesis process. This allows for the sequential addition of amino acids to build peptides with high precision. The D-configuration of Abu (α-aminobutyric acid) makes it valuable in creating peptides with specific stereochemistry, which is crucial for studying biological activity and structure-activity relationships. Additionally, it is employed in the development of peptide-based drugs, peptidomimetics, and biochemical research, where the incorporation of non-natural amino acids is required to enhance stability, bioavailability, or target specificity.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Powder |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | €7.91 |
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| 5.000 | 10-20 days | €13.72 |
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| 25.000 | 10-20 days | €61.73 |
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Fmoc-D-Abu-OH
Fmoc-D-Abu-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality during the synthesis process. This allows for the sequential addition of amino acids to build peptides with high precision. The D-configuration of Abu (α-aminobutyric acid) makes it valuable in creating peptides with specific stereochemistry, which is crucial for studying biological activity and structure-activity relationships. Additionally, it is employed in the development of peptide-based drugs, peptidomimetics, and biochemical research, where the incorporation of non-natural amino acids is required to enhance stability, bioavailability, or target specificity.
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