Boc-L-Lys(2-Cl-Z)-OH
98%
- Product Code: 126681
Alias:
N-tert-butoxycarbonyl-N'-(2-chlorobenzyloxycarbonyl)-L-lysine ; Nα-BOC-Nε-(2-chloro-CBZ)-L-lysine
CAS:
54613-99-9
| Molecular Weight: | 414.88 g./mol | Molecular Formula: | C₁₉H₂₇ClN₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00038386 | |
| Melting Point: | 70-73 °C | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, where the Boc (tert-butyloxycarbonyl) group protects the amino group, and the 2-Cl-Z (2-chlorobenzyloxycarbonyl) group protects the side chain of lysine. This dual protection allows selective deprotection during peptide chain assembly, ensuring precise control over the synthesis process. It is particularly valuable in producing complex peptides for research, pharmaceuticals, and biotechnology applications, where maintaining the integrity of the lysine residue is critical. Its stability and ease of handling make it a preferred choice in solid-phase peptide synthesis (SPPS) and other peptide-related methodologies.
Product Specification:
| Test | Specification |
|---|---|
| Melting Point | 70-75 |
| Purity (HPLC) | 98-100 |
| Specific Rotation [A]20/D(C=2, DMF) | 10-14 |
| Appearance | White To Off-White Powder |
| TLC Analysis | One Spot |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | $50.72 |
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| 25.000 | 10-20 days | $194.90 |
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| 100.000 | 10-20 days | $483.73 |
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Boc-L-Lys(2-Cl-Z)-OH
This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, where the Boc (tert-butyloxycarbonyl) group protects the amino group, and the 2-Cl-Z (2-chlorobenzyloxycarbonyl) group protects the side chain of lysine. This dual protection allows selective deprotection during peptide chain assembly, ensuring precise control over the synthesis process. It is particularly valuable in producing complex peptides for research, pharmaceuticals, and biotechnology applications, where maintaining the integrity of the lysine residue is critical. Its stability and ease of handling make it a preferred choice in solid-phase peptide synthesis (SPPS) and other peptide-related methodologies.
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