Boc-4-Amino-L-phenylalanine
98%
- Product Code: 104665
Alias:
BOC-4-amino-L-phenylalanine ;N-tert-butoxycarbonyl-4-amino-L-phenylalanine,N-tert-butoxycarbonyl-4-amino-L-phenylalanine
CAS:
55533-24-9
| Molecular Weight: | 280.32 g./mol | Molecular Formula: | C₁₄H₂₀N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00038139 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C |
Product Description:
Boc-4-Amino-L-phenylalanine is widely used in peptide synthesis as a protected amino acid. The Boc (tert-butyloxycarbonyl) group serves as a protective group for the amino functionality, preventing unwanted reactions during peptide chain assembly. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it allows for the controlled and sequential addition of amino acids to build complex peptides. After the peptide chain is assembled, the Boc group can be selectively removed under mild acidic conditions, revealing the free amino group for further reactions. Additionally, it is employed in the synthesis of modified peptides and peptidomimetics, where precise control over amino acid incorporation is essential. Its application extends to the development of pharmaceuticals, bioactive peptides, and research tools in biochemistry and molecular biology.
Product Specification:
| Test | Specification |
|---|---|
| Melting Point | 125-131 |
| Purity (HPLC) | 98-100 |
| Specific Rotation | 23-29 |
| Appearance | White To Pale Yellow Powder |
| Infrared Spectrum | Conforms To Structure |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿620.00 |
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| 5.000 | 10-20 days | ฿2,240.00 |
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| 25.000 | 10-20 days | ฿9,860.00 |
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Boc-4-Amino-L-phenylalanine
Boc-4-Amino-L-phenylalanine is widely used in peptide synthesis as a protected amino acid. The Boc (tert-butyloxycarbonyl) group serves as a protective group for the amino functionality, preventing unwanted reactions during peptide chain assembly. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it allows for the controlled and sequential addition of amino acids to build complex peptides. After the peptide chain is assembled, the Boc group can be selectively removed under mild acidic conditions, revealing the free amino group for further reactions. Additionally, it is employed in the synthesis of modified peptides and peptidomimetics, where precise control over amino acid incorporation is essential. Its application extends to the development of pharmaceuticals, bioactive peptides, and research tools in biochemistry and molecular biology.
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