Nα-(tert-Butoxycarbonyl)-L-tryptophan N-Succinimidyl Ester
98%
- Product Code: 59187
CAS:
3392-11-8
Molecular Weight: | 401.42 g./mol | Molecular Formula: | C₂₀H₂₃N₃O₆ |
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EC Number: | MDL Number: | MFCD00022756 | |
Melting Point: | 145°C | Boiling Point: | |
Density: | Storage Condition: | -20°C |
Product Description:
Used extensively in peptide synthesis, this compound acts as a protected amino acid derivative, facilitating the incorporation of tryptophan into peptide chains. Its tert-butoxycarbonyl (Boc) group provides protection for the amino group during synthesis, while the succinimidyl ester moiety enhances reactivity, enabling efficient coupling with other amino acids or peptides. It is particularly valuable in solid-phase peptide synthesis (SPPS) for creating complex peptides and proteins with high precision. Additionally, it is employed in the development of pharmaceuticals, bioactive peptides, and research tools for studying protein interactions and functions. Its stability and reactivity make it a preferred choice in organic and medicinal chemistry applications.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | €55.56 |
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Nα-(tert-Butoxycarbonyl)-L-tryptophan N-Succinimidyl Ester
Used extensively in peptide synthesis, this compound acts as a protected amino acid derivative, facilitating the incorporation of tryptophan into peptide chains. Its tert-butoxycarbonyl (Boc) group provides protection for the amino group during synthesis, while the succinimidyl ester moiety enhances reactivity, enabling efficient coupling with other amino acids or peptides. It is particularly valuable in solid-phase peptide synthesis (SPPS) for creating complex peptides and proteins with high precision. Additionally, it is employed in the development of pharmaceuticals, bioactive peptides, and research tools for studying protein interactions and functions. Its stability and reactivity make it a preferred choice in organic and medicinal chemistry applications.
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