Boc-D-Asp(OBzl)-OH
98%
- Product Code: 105725
Alias:
tert-Butoxycarbonyl-D-Aspartic Acid 4-Benzyl Ester ; BOC-D-Aspartic Acid β-Benzyl Ester
CAS:
51186-58-4
| Molecular Weight: | 323.34 g./mol | Molecular Formula: | C₁₆H₂₁NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00038255 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8°C |
Product Description:
Used in peptide synthesis as a protected form of aspartic acid, ensuring specific amino acid incorporation without unwanted side reactions. It is particularly valuable in solid-phase peptide synthesis (SPPS) for constructing complex peptides or proteins. The Boc (tert-butyloxycarbonyl) group protects the amine functionality, while the OBzl (benzyl) group safeguards the carboxyl side chain, allowing selective deprotection during synthesis. This compound is essential in producing peptides for pharmaceutical research, drug development, and biochemical studies, where precise control over peptide sequences is critical. Its stability and compatibility with various coupling reagents make it a reliable choice for synthesizing peptides with aspartic acid residues.
Product Specification:
| Test | Specification |
|---|---|
| Carbon By Elemental Analysis | 57.6-59.8 |
| Hydrogen By Elemental Analysis | 6-6.7 |
| Nitrogen | 4-4.6 |
| Oxygen By Elemental Analysis | 28.6-30.1 |
| Purity (HPLC) | 98-100 |
| Appearance | White to off-white powder or solid or chunks |
| Infrared Spectrometry | Conforms to Structure |
| Proton NMR Spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿350.00 |
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| 5.000 | 10-20 days | ฿990.00 |
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Boc-D-Asp(OBzl)-OH
Used in peptide synthesis as a protected form of aspartic acid, ensuring specific amino acid incorporation without unwanted side reactions. It is particularly valuable in solid-phase peptide synthesis (SPPS) for constructing complex peptides or proteins. The Boc (tert-butyloxycarbonyl) group protects the amine functionality, while the OBzl (benzyl) group safeguards the carboxyl side chain, allowing selective deprotection during synthesis. This compound is essential in producing peptides for pharmaceutical research, drug development, and biochemical studies, where precise control over peptide sequences is critical. Its stability and compatibility with various coupling reagents make it a reliable choice for synthesizing peptides with aspartic acid residues.
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