L-Glutamine t-butyl ester hydrochloride
98%
- Product Code: 105373
Alias:
L-glutamine tert-butyl ester hydrochloride
CAS:
39741-62-3
| Molecular Weight: | 238.71 g./mol | Molecular Formula: | C₉H₁₈N₂O₃HCl |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00039081 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C |
Product Description:
L-Glutamine t-butyl ester hydrochloride is widely used in peptide synthesis as a protective group for the carboxyl function of glutamine. It helps in preventing unwanted side reactions during the formation of peptide bonds, ensuring higher purity and yield of the final peptide product. This compound is particularly valuable in the production of complex peptides and proteins for pharmaceutical research and drug development. Additionally, it is utilized in the synthesis of bioactive peptides, which are essential for studying cellular processes and developing therapeutic agents. Its stability and ease of removal make it a preferred choice in solid-phase peptide synthesis.
Product Specification:
| Test | Specification |
|---|---|
| Purity (HPLC) | 98-100 |
| Specific Rotation [A]20/D(C=2, ETOH) | +13.3±1 Degree Celsius |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿2,890.00 |
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L-Glutamine t-butyl ester hydrochloride
L-Glutamine t-butyl ester hydrochloride is widely used in peptide synthesis as a protective group for the carboxyl function of glutamine. It helps in preventing unwanted side reactions during the formation of peptide bonds, ensuring higher purity and yield of the final peptide product. This compound is particularly valuable in the production of complex peptides and proteins for pharmaceutical research and drug development. Additionally, it is utilized in the synthesis of bioactive peptides, which are essential for studying cellular processes and developing therapeutic agents. Its stability and ease of removal make it a preferred choice in solid-phase peptide synthesis.
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