Boc-N-Me-Arg(Mtr)-OH
98%
- Product Code: 59166
CAS:
125602-26-8
| Molecular Weight: | 500.62 g./mol | Molecular Formula: | C₂₂H₃₆N₄O₇S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00236863 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, particularly in solid-phase peptide synthesis (SPPS). The Boc (tert-butoxycarbonyl) group protects the amino group, while the Mtr (4-methoxy-2,3,6-trimethylbenzenesulfonyl) group safeguards the guanidine function of the arginine side chain. This protection ensures selective reactions during peptide chain assembly, preventing unwanted side reactions. It is especially useful in synthesizing peptides containing arginine residues, which are common in biologically active peptides and proteins. After peptide synthesis, the protecting groups can be removed under specific conditions to yield the desired peptide sequence. Its application is critical in pharmaceutical research, drug development, and the study of protein-protein interactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $578.60 |
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Boc-N-Me-Arg(Mtr)-OH
This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, particularly in solid-phase peptide synthesis (SPPS). The Boc (tert-butoxycarbonyl) group protects the amino group, while the Mtr (4-methoxy-2,3,6-trimethylbenzenesulfonyl) group safeguards the guanidine function of the arginine side chain. This protection ensures selective reactions during peptide chain assembly, preventing unwanted side reactions. It is especially useful in synthesizing peptides containing arginine residues, which are common in biologically active peptides and proteins. After peptide synthesis, the protecting groups can be removed under specific conditions to yield the desired peptide sequence. Its application is critical in pharmaceutical research, drug development, and the study of protein-protein interactions.
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