Fmoc-L-beta-Homovaline
98%
- Product Code: 105081
Alias:
Fmoc-L-beta-homovaline; Fmoc-L-beta-leucine, (R)-3-(N-fluorenylmethoxycarbonylamino)-4-methylpentanoic acid
CAS:
172695-33-9
| Molecular Weight: | 353.41 g./mol | Molecular Formula: | C₂₁H₂₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01862853 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed and dry |
Product Description:
Fmoc-L-beta-Homovaline is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methodologies. The Fmoc (fluorenylmethyloxycarbonyl) group serves as a protective group for the amino group during the synthesis process, allowing for the stepwise construction of peptides. This compound is valuable in the production of custom peptides for research and pharmaceutical applications, enabling the incorporation of beta-homovaline, a non-natural amino acid, into peptide sequences. Its use facilitates the study of peptide structure-activity relationships, the development of peptide-based drugs, and the exploration of novel biomaterials. Additionally, it is employed in the synthesis of peptidomimetics, which are compounds that mimic the structure and function of peptides, often with enhanced stability or bioavailability.
Product Specification:
| Test | Specification |
|---|---|
| Purity (HPLC) | 97-100 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,782.00 |
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| 0.250 | 10-20 days | ฿2,628.00 |
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Fmoc-L-beta-Homovaline
Fmoc-L-beta-Homovaline is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methodologies. The Fmoc (fluorenylmethyloxycarbonyl) group serves as a protective group for the amino group during the synthesis process, allowing for the stepwise construction of peptides. This compound is valuable in the production of custom peptides for research and pharmaceutical applications, enabling the incorporation of beta-homovaline, a non-natural amino acid, into peptide sequences. Its use facilitates the study of peptide structure-activity relationships, the development of peptide-based drugs, and the exploration of novel biomaterials. Additionally, it is employed in the synthesis of peptidomimetics, which are compounds that mimic the structure and function of peptides, often with enhanced stability or bioavailability.
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