N(alpha)-boc-L-arginine
98%
- Product Code: 77604
CAS:
13726-76-6
| Molecular Weight: | 274.32 g./mol | Molecular Formula: | HNCNH₂NHCH₂₃CHCOOHNHCOOCCH₃₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00042632 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
N(alpha)-boc-L-arginine is widely used in peptide synthesis as a protected form of L-arginine. The Boc (tert-butyloxycarbonyl) group acts as a protective shield for the amino group during the synthesis process, preventing unwanted reactions. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it ensures the selective formation of peptide bonds. Additionally, it is employed in the production of bioactive peptides and pharmaceutical intermediates, where precise control over amino acid incorporation is essential. Its stability and ease of deprotection make it a preferred choice in research and industrial applications related to peptide chemistry.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Yellow Powder |
| PURITY | 97.5-100 |
| PROTON NMR SPECTRUM | Conforms to Structure |
| Infrared spectrum | Conforms to Structure |
| SOLUBILITY IN METHANOL | Colorless to Yellow-Green,Clear,100mg/ml |
| Specific rotation a20DC1 Acetic Acid | -6.5 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿2,450.00 |
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| 25.000 | 10-20 days | ฿8,390.00 |
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N(alpha)-boc-L-arginine
N(alpha)-boc-L-arginine is widely used in peptide synthesis as a protected form of L-arginine. The Boc (tert-butyloxycarbonyl) group acts as a protective shield for the amino group during the synthesis process, preventing unwanted reactions. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it ensures the selective formation of peptide bonds. Additionally, it is employed in the production of bioactive peptides and pharmaceutical intermediates, where precise control over amino acid incorporation is essential. Its stability and ease of deprotection make it a preferred choice in research and industrial applications related to peptide chemistry.
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