Fmoc-D-Lys(Dde)-OH
97%
- Product Code: 97555
CAS:
150629-67-7
| Molecular Weight: | 532.63 g./mol | Molecular Formula: | C₃₁H₃₆N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00278818 | |
| Melting Point: | 80°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound 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 protects the amino group, and the Dde (1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyl) group protects the side chain amine of lysine. This dual protection allows for selective deprotection, enabling the controlled synthesis of complex peptides. It is especially valuable in the synthesis of peptides that require orthogonal protection strategies, such as those involving multiple lysine residues or post-synthetic modifications. Its application is critical in producing peptides for pharmaceutical research, drug development, and biochemical studies.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Light yellow powder to crystal |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $20.84 |
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| 1.000 | 10-20 days | $57.42 |
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| 5.000 | 10-20 days | $274.50 |
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Fmoc-D-Lys(Dde)-OH
This compound 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 protects the amino group, and the Dde (1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyl) group protects the side chain amine of lysine. This dual protection allows for selective deprotection, enabling the controlled synthesis of complex peptides. It is especially valuable in the synthesis of peptides that require orthogonal protection strategies, such as those involving multiple lysine residues or post-synthetic modifications. Its application is critical in producing peptides for pharmaceutical research, drug development, and biochemical studies.
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