Fmoc-D-Leu-OH
98%
- Product Code: 105040
Alias:
N-[(9H-fluorenylmethoxy)carbonyl]-D-leucine, N-Fmoc-D-leucine, fluorenylmethoxycarbonyl-D-leucine, N-fluorenylmethoxycarbonyl- D-leucine, Nα-(9-fluorenylmethoxycarbonyl)-D-leucine
CAS:
114360-54-2
| Molecular Weight: | 353.42 g./mol | Molecular Formula: | C₂₁H₂₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00062957 | |
| Melting Point: | 155°C | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
Fmoc-D-Leu-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected form of D-leucine, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino acid’s amine functionality. This allows for the sequential addition of amino acids to build peptides with high precision. The compound is especially valuable in the production of peptides with D-amino acids, which are often used in research to study peptide stability, biological activity, and enzyme resistance. Additionally, Fmoc-D-Leu-OH is employed in the development of peptidomimetics and therapeutic peptides, where the incorporation of D-amino acids can enhance metabolic stability and bioavailability. Its role in peptide synthesis makes it a crucial reagent in pharmaceutical research and drug development.
Product Specification:
| Test | Specification |
|---|---|
| Melting Point | 153-157 |
| Purity (HPLC) | 98-100 |
| Purity (Neutralization Titration) | 98-100 |
| Specific Rotation | 22-23 |
| Infrared Spectrometry | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿320.00 |
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| 5.000 | 10-20 days | ฿490.00 |
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| 25.000 | 10-20 days | ฿1,760.00 |
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| 100.000 | 10-20 days | ฿6,400.00 |
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Fmoc-D-Leu-OH
Fmoc-D-Leu-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected form of D-leucine, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino acid’s amine functionality. This allows for the sequential addition of amino acids to build peptides with high precision. The compound is especially valuable in the production of peptides with D-amino acids, which are often used in research to study peptide stability, biological activity, and enzyme resistance. Additionally, Fmoc-D-Leu-OH is employed in the development of peptidomimetics and therapeutic peptides, where the incorporation of D-amino acids can enhance metabolic stability and bioavailability. Its role in peptide synthesis makes it a crucial reagent in pharmaceutical research and drug development.
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