H-Lys(Z)-OBzl hydrochloride
97%
- Product Code: 59211
Alias:
Nε-CBZ-L-lysine benzyl ester hydrochloride; N6-benzyloxycarbonyl-L-lysine benzyl ester hydrochloride
CAS:
6366-70-7
| Molecular Weight: | 406.9 g./mol | Molecular Formula: | C₂₁H₂₆N₂O₄HCl |
|---|---|---|---|
| EC Number: | 228-859-9 | MDL Number: | MFCD00038981 |
| Melting Point: | 138-140 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in peptide synthesis as a protected form of lysine. The benzyloxycarbonyl (Z) group protects the amino group of lysine, preventing unwanted reactions during peptide chain assembly. The benzyl ester (OBzl) protects the carboxyl group, ensuring selective coupling reactions. It is particularly useful in solid-phase peptide synthesis (SPPS) and solution-phase synthesis, where controlled deprotection is required. The hydrochloride form enhances its stability and solubility in various solvents, making it easier to handle in laboratory settings. Its applications extend to the production of bioactive peptides, pharmaceuticals, and research reagents in biochemistry and molecular biology.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Off-White Powder |
| PURITY | 96.5-100 |
| MELTING POINT | 138-141 |
| Infrared spectrum | Conforms to Structure |
| Specific rotation a20DC1 in 0.1N HCl | -5.5 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | $42.36 |
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| 25.000 | 10-20 days | $104.24 |
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| 100.000 | 10-20 days | $338.88 |
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H-Lys(Z)-OBzl hydrochloride
This compound is primarily utilized in peptide synthesis as a protected form of lysine. The benzyloxycarbonyl (Z) group protects the amino group of lysine, preventing unwanted reactions during peptide chain assembly. The benzyl ester (OBzl) protects the carboxyl group, ensuring selective coupling reactions. It is particularly useful in solid-phase peptide synthesis (SPPS) and solution-phase synthesis, where controlled deprotection is required. The hydrochloride form enhances its stability and solubility in various solvents, making it easier to handle in laboratory settings. Its applications extend to the production of bioactive peptides, pharmaceuticals, and research reagents in biochemistry and molecular biology.
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