Fmoc-Dap(Alloc)-OH
95%
- Product Code: 96207
Alias:
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(((allyloxy)carbonyl)amino)propanoic acid
CAS:
188970-92-5
| Molecular Weight: | 410.42 g./mol | Molecular Formula: | C₂₂H₂₂N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00273468 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C |
Product Description:
Fmoc-Dap(Alloc)-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc group safeguards the amine functionality during the assembly of the peptide chain. The Alloc group provides additional protection for the side chain of diaminopropionic acid (Dap), allowing for selective deprotection and further modification when needed. This compound is especially valuable in the synthesis of complex peptides and peptidomimetics, where precise control over side-chain reactivity is essential. Its application is critical in the development of therapeutic peptides, bioactive molecules, and research tools in biochemistry and medicinal chemistry.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Yellow Solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $31.07 |
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| 1.000 | 10-20 days | $93.99 |
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| 5.000 | 10-20 days | $434.55 |
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Fmoc-Dap(Alloc)-OH
Fmoc-Dap(Alloc)-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc group safeguards the amine functionality during the assembly of the peptide chain. The Alloc group provides additional protection for the side chain of diaminopropionic acid (Dap), allowing for selective deprotection and further modification when needed. This compound is especially valuable in the synthesis of complex peptides and peptidomimetics, where precise control over side-chain reactivity is essential. Its application is critical in the development of therapeutic peptides, bioactive molecules, and research tools in biochemistry and medicinal chemistry.
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