H-D-Ser-OBzl.HCl
97%
- Product Code: 50390
CAS:
151651-44-4
| Molecular Weight: | 231.68 g./mol | Molecular Formula: | C₁₀H₁₄ClNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00191017 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
This compound is primarily utilized in peptide synthesis, where it serves as a protected form of serine. The benzyl (Bzl) group acts as a protective group for the hydroxyl side chain of serine, preventing unwanted reactions during the peptide assembly process. The hydrochloride (HCl) salt form enhances its stability and solubility, making it easier to handle in organic synthesis. It is commonly employed in the production of custom peptides for research purposes, particularly in the development of pharmaceuticals and biochemical studies. Its role is critical in ensuring the precise and efficient construction of peptide chains, particularly when serine residues are required in specific positions.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿880.00 |
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| 5.000 | 10-20 days | ฿3,300.00 |
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| 10.000 | 10-20 days | ฿5,130.00 |
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| 25.000 | 10-20 days | ฿12,000.00 |
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H-D-Ser-OBzl.HCl
This compound is primarily utilized in peptide synthesis, where it serves as a protected form of serine. The benzyl (Bzl) group acts as a protective group for the hydroxyl side chain of serine, preventing unwanted reactions during the peptide assembly process. The hydrochloride (HCl) salt form enhances its stability and solubility, making it easier to handle in organic synthesis. It is commonly employed in the production of custom peptides for research purposes, particularly in the development of pharmaceuticals and biochemical studies. Its role is critical in ensuring the precise and efficient construction of peptide chains, particularly when serine residues are required in specific positions.
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