Fmoc-Dap(Alloc)-OH
≥98.5% (HPLC)
- Product Code: 96093
Alias:
Nβ-Alloc-Nα-Fmoc-L-2,3-diaminopropionic acid Nβ-allyloxycarbonyl-Nα-Fmoc-L-2,3-diaminopropionic acid N-fluorenylmethoxycarbonyl-3-[ [(allyloxy)carbonyl]amino]-L-alanine
CAS:
188970-92-5
Molecular Weight: | 410.42 g./mol | Molecular Formula: | C₂₂H₂₂N₂O₆ |
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EC Number: | MDL Number: | MFCD00273468 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | -20°C |
Product Description:
This chemical 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 group protects the amino group during the synthesis process, while the Alloc group protects the side chain. This dual protection allows for selective deprotection, enabling the synthesis of complex peptides with high precision. It is especially valuable in the production of peptides with specific sequences or modifications, such as those used in pharmaceutical research, drug development, and biochemical studies. Its application ensures efficient and controlled peptide chain assembly, making it a critical component in the synthesis of therapeutic peptides and peptidomimetics.
Product Specification:
Test | Specification |
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PURITYHPLC | 98.5 100% |
INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿1,134.00 |
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Fmoc-Dap(Alloc)-OH
This chemical 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 group protects the amino group during the synthesis process, while the Alloc group protects the side chain. This dual protection allows for selective deprotection, enabling the synthesis of complex peptides with high precision. It is especially valuable in the production of peptides with specific sequences or modifications, such as those used in pharmaceutical research, drug development, and biochemical studies. Its application ensures efficient and controlled peptide chain assembly, making it a critical component in the synthesis of therapeutic peptides and peptidomimetics.
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