Fmoc-L-aspartic acid β-benzyl ester
99%
- Product Code: 105167
Alias:
Fmoc-aspartic acid-β-benzyl ester ; Fmoc-aspartic acid-β-benzyl ester
CAS:
86060-84-6
| Molecular Weight: | 445.46 g./mol | Molecular Formula: | C₂₆H₂₃NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00065630 | |
| Melting Point: | 120-130 °C | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
Fmoc-L-aspartic acid β-benzyl ester is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected form of aspartic acid, where the Fmoc (fluorenylmethyloxycarbonyl) group protects the amino group, and the benzyl ester protects the carboxyl group. This protection ensures selective reactions during peptide chain assembly. The compound is especially valuable in synthesizing peptides with aspartic acid residues, as it prevents unwanted side reactions. After peptide synthesis, the protecting groups can be removed under mild conditions, making it a versatile and essential reagent in the production of complex peptides for research, pharmaceuticals, and biotechnology applications.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White Solid |
| Purity (%) | 98.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿360.00 |
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| 5.000 | 10-20 days | ฿950.00 |
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| 25.000 | 10-20 days | ฿3,500.00 |
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| 100.000 | 10-20 days | ฿13,880.00 |
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Fmoc-L-aspartic acid β-benzyl ester
Fmoc-L-aspartic acid β-benzyl ester is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected form of aspartic acid, where the Fmoc (fluorenylmethyloxycarbonyl) group protects the amino group, and the benzyl ester protects the carboxyl group. This protection ensures selective reactions during peptide chain assembly. The compound is especially valuable in synthesizing peptides with aspartic acid residues, as it prevents unwanted side reactions. After peptide synthesis, the protecting groups can be removed under mild conditions, making it a versatile and essential reagent in the production of complex peptides for research, pharmaceuticals, and biotechnology applications.
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