Fmoc-β-Homogln(Trt)-OH
98%
- Product Code: 104092
Alias:
Nβ-Fmoc-Nε-trityl-L-homoglutamine
CAS:
401915-55-7
| Molecular Weight: | 624.72 g./mol | Molecular Formula: | C₄₀H₃₆N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03427580 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8°C |
Product Description:
This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (9-fluorenylmethoxycarbonyl) group protects the amino group, and the Trt (trityl) group protects the side chain. This protection allows for selective deprotection and coupling during the stepwise assembly of peptides. It is especially valuable in synthesizing peptides containing β-homoglutamine, a non-natural amino acid, which can be incorporated into peptides to study structure-activity relationships or to modify peptide properties such as stability, solubility, or biological activity. Its use is common in pharmaceutical research, drug development, and biochemical studies where precise peptide sequences are required.
Product Specification:
| Test | Specification |
|---|---|
| Melting Point | 113-117 |
| Purity (HPLC) | 95-100 |
| Infrared Spectrometry | Conforms To Structure |
| Proton NMR Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,640.00 |
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Fmoc-β-Homogln(Trt)-OH
This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (9-fluorenylmethoxycarbonyl) group protects the amino group, and the Trt (trityl) group protects the side chain. This protection allows for selective deprotection and coupling during the stepwise assembly of peptides. It is especially valuable in synthesizing peptides containing β-homoglutamine, a non-natural amino acid, which can be incorporated into peptides to study structure-activity relationships or to modify peptide properties such as stability, solubility, or biological activity. Its use is common in pharmaceutical research, drug development, and biochemical studies where precise peptide sequences are required.
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