(S)-Fmoc-2-amino-5-(trityl-carbamoyl)pentanoic acid
95%
- Product Code: 78482
CAS:
1263046-43-0
| Molecular Weight: | 624.72 g./mol | Molecular Formula: | C₄₀H₃₆N₂O₅ |
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| EC Number: | MDL Number: | MFCD03093573 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used primarily in peptide synthesis, this compound acts as a protected amino acid derivative, enabling the construction of complex peptides with high precision. Its Fmoc group provides temporary protection for the amino group during synthesis, while the trityl group safeguards the carbamoyl functionality, preventing unwanted side reactions. This chemical is particularly valuable in solid-phase peptide synthesis (SPPS), where it ensures the stepwise addition of amino acids with minimal interference. It is also employed in the development of peptide-based drugs, biomaterials, and research tools, offering versatility in designing custom peptide sequences for therapeutic or experimental purposes. Its stability and compatibility with standard synthesis protocols make it a reliable choice for chemists working in peptide chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $205.42 |
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| 0.250 | 10-20 days | $329.69 |
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| 1.000 | 10-20 days | $853.38 |
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(S)-Fmoc-2-amino-5-(trityl-carbamoyl)pentanoic acid
Used primarily in peptide synthesis, this compound acts as a protected amino acid derivative, enabling the construction of complex peptides with high precision. Its Fmoc group provides temporary protection for the amino group during synthesis, while the trityl group safeguards the carbamoyl functionality, preventing unwanted side reactions. This chemical is particularly valuable in solid-phase peptide synthesis (SPPS), where it ensures the stepwise addition of amino acids with minimal interference. It is also employed in the development of peptide-based drugs, biomaterials, and research tools, offering versatility in designing custom peptide sequences for therapeutic or experimental purposes. Its stability and compatibility with standard synthesis protocols make it a reliable choice for chemists working in peptide chemistry.
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