Z-Lys(Boc)-OH
97%
- Product Code: 105631
Alias:
Z-butoxycarbonyllysine; N2-benzyloxycarbonyl-N6-tert-butylcarbonyl-L-lysine, Nα-CBZ-Nε-BOC-D-lysine
CAS:
2389-60-8
| Molecular Weight: | 380.44 g./mol | Molecular Formula: | C₁₉H₂₈N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00062271 | |
| Melting Point: | 63-70°C | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
This chemical is primarily used in peptide synthesis as a protected form of lysine. It serves as a building block in the creation of peptides, ensuring that the lysine side chain remains protected during the synthesis process. The Boc (tert-butyloxycarbonyl) group safeguards the amino group, preventing unwanted reactions while allowing the carboxyl group to participate in peptide bond formation. It is particularly useful in solid-phase peptide synthesis (SPPS) and solution-phase synthesis, where selective deprotection is required. This compound is essential in producing peptides for research, pharmaceuticals, and biotechnology applications, enabling the development of peptide-based drugs, vaccines, and biochemical studies. Its stability and compatibility with various synthesis methods make it a valuable reagent in organic and medicinal chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Almost White Powder To Crystal |
| Purity (HPLC) | 98-100 |
| Purity (Neutralization Titration) | 98-100 |
| Infrared Spectrum | Conforms To Structure |
| Solubility In Methanol | Almost Transparency |
| Specific Rotation [a]20/D(C=1, MeOH) | -4 To -7 |
| Melting Point | 60.0-64.0 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿340.00 |
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| 5.000 | 10-20 days | ฿1,070.00 |
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| 25.000 | 10-20 days | ฿4,640.00 |
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| 100.000 | 10-20 days | ฿14,600.00 |
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Z-Lys(Boc)-OH
This chemical is primarily used in peptide synthesis as a protected form of lysine. It serves as a building block in the creation of peptides, ensuring that the lysine side chain remains protected during the synthesis process. The Boc (tert-butyloxycarbonyl) group safeguards the amino group, preventing unwanted reactions while allowing the carboxyl group to participate in peptide bond formation. It is particularly useful in solid-phase peptide synthesis (SPPS) and solution-phase synthesis, where selective deprotection is required. This compound is essential in producing peptides for research, pharmaceuticals, and biotechnology applications, enabling the development of peptide-based drugs, vaccines, and biochemical studies. Its stability and compatibility with various synthesis methods make it a valuable reagent in organic and medicinal chemistry.
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