Nalpha-Boc-Nomega-nitro-D-arginine
≥97%
- Product Code: 76580
CAS:
50913-12-7
| Molecular Weight: | 319.31 g./mol | Molecular Formula: | C₁₁H₂₁N₅O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00038091 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used in peptide synthesis as a protected form of D-arginine. The Boc (tert-butoxycarbonyl) group safeguards the amino group during the synthesis process, while the nitro group protects the guanidine moiety. It is particularly valuable in creating peptides with specific configurations, as the D-arginine enantiomer can influence the peptide's biological activity and stability. Additionally, it is employed in research to study enzyme-substrate interactions, particularly in cases where arginine plays a critical role, such as in nitric oxide synthase studies. Its protective groups allow for selective deprotection, enabling precise control over the synthesis of complex peptide structures.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White Powder |
| PURITY | 97 |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | £22.16 |
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| 1.000 | 10-20 days | £86.40 |
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| 5.000 | 10-20 days | £221.19 |
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Nalpha-Boc-Nomega-nitro-D-arginine
This chemical is primarily used in peptide synthesis as a protected form of D-arginine. The Boc (tert-butoxycarbonyl) group safeguards the amino group during the synthesis process, while the nitro group protects the guanidine moiety. It is particularly valuable in creating peptides with specific configurations, as the D-arginine enantiomer can influence the peptide's biological activity and stability. Additionally, it is employed in research to study enzyme-substrate interactions, particularly in cases where arginine plays a critical role, such as in nitric oxide synthase studies. Its protective groups allow for selective deprotection, enabling precise control over the synthesis of complex peptide structures.
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