Ac-Lys(Boc)-OH
96%
- Product Code: 38197
CAS:
23500-04-1
| Molecular Weight: | 288.34 g./mol | Molecular Formula: | C₁₃H₂₄N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00236761 | |
| Melting Point: | Boiling Point: | 528.8°C at 760 mmHg | |
| Density: | Storage Condition: | -20°C, store under inert gas |
Product Description:
This chemical is widely used in peptide synthesis as a protecting group for lysine residues. The Boc (tert-butyloxycarbonyl) group shields the amino group of lysine, preventing unwanted reactions during the peptide chain assembly. It is particularly valuable in solid-phase peptide synthesis (SPPS) and solution-phase synthesis, ensuring selective deprotection and coupling steps. Additionally, it is employed in the production of modified peptides and peptidomimetics for research in drug development, biochemistry, and molecular biology. Its stability under acidic conditions makes it a reliable choice for complex peptide constructions.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white solid |
| PURITY | 95.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿840.00 |
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| 5.000 | 10-20 days | ฿3,310.00 |
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| 10.000 | 10-20 days | ฿5,080.00 |
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| 25.000 | 10-20 days | ฿6,800.00 |
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Ac-Lys(Boc)-OH
This chemical is widely used in peptide synthesis as a protecting group for lysine residues. The Boc (tert-butyloxycarbonyl) group shields the amino group of lysine, preventing unwanted reactions during the peptide chain assembly. It is particularly valuable in solid-phase peptide synthesis (SPPS) and solution-phase synthesis, ensuring selective deprotection and coupling steps. Additionally, it is employed in the production of modified peptides and peptidomimetics for research in drug development, biochemistry, and molecular biology. Its stability under acidic conditions makes it a reliable choice for complex peptide constructions.
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