Fmoc-Asp(OMpe)-OH
97%
- Product Code: 51167
CAS:
180675-08-5
| Molecular Weight: | 439.50 g./mol | Molecular Formula: | C₂₅H₂₉NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD10001333 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, dry sealed |
Product Description:
This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected form of aspartic acid, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino group, and the OMpe (4-methoxyphenethyl) group protects the side chain carboxyl group. This protection strategy is crucial for ensuring selective reactions during the stepwise assembly of peptides, preventing unwanted side reactions. It is especially valuable in the synthesis of complex peptides and proteins, where precise control over the sequence and structure is required. Additionally, it finds applications in the development of pharmaceuticals, bioactive peptides, and research tools for studying protein function and interactions. Its stability and compatibility with SPPS make it a preferred choice in both academic and industrial settings.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $25.75 |
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| 0.250 | 10-20 days | $52.74 |
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| 1.000 | 10-20 days | $125.42 |
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| 5.000 | 10-20 days | $388.30 |
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Fmoc-Asp(OMpe)-OH
This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected form of aspartic acid, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino group, and the OMpe (4-methoxyphenethyl) group protects the side chain carboxyl group. This protection strategy is crucial for ensuring selective reactions during the stepwise assembly of peptides, preventing unwanted side reactions. It is especially valuable in the synthesis of complex peptides and proteins, where precise control over the sequence and structure is required. Additionally, it finds applications in the development of pharmaceuticals, bioactive peptides, and research tools for studying protein function and interactions. Its stability and compatibility with SPPS make it a preferred choice in both academic and industrial settings.
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