Fmoc-N-methyl-L-valine
98%
- Product Code: 105128
Alias:
Fmoc-N-methyl-L-valine ; N-fluorenylmethoxycarbonyl-N-methyl-L-valine
CAS:
84000-11-3
| Molecular Weight: | 353.41 g./mol | Molecular Formula: | C₂₁H₂₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00153395 | |
| Melting Point: | 187-190 °C | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
Fmoc-N-methyl-L-valine is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality. This allows for the sequential addition of amino acids to build peptides with high precision. The N-methyl group in the structure introduces steric hindrance, which can be beneficial in designing peptides with specific conformational properties or enhanced metabolic stability. This compound is especially valuable in the synthesis of complex peptides, including those used in pharmaceutical research, where controlled assembly and modification of peptide chains are critical. Its application extends to the development of peptide-based drugs, biomaterials, and probes for biochemical studies.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Off-White Powder |
| Purity (HPLC) | 98-100 |
| Melting Point | 180-190 |
| Infrared Spectrum | Conforms To Structure |
| Specific Rotation [A]20/D(C=1,DMF) | -65 Degree Celsius -71 Degree Celsius |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿410.00 |
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| 5.000 | 10-20 days | ฿1,490.00 |
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| 25.000 | 10-20 days | ฿5,980.00 |
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| 100.000 | 10-20 days | ฿22,960.00 |
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Fmoc-N-methyl-L-valine
Fmoc-N-methyl-L-valine is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality. This allows for the sequential addition of amino acids to build peptides with high precision. The N-methyl group in the structure introduces steric hindrance, which can be beneficial in designing peptides with specific conformational properties or enhanced metabolic stability. This compound is especially valuable in the synthesis of complex peptides, including those used in pharmaceutical research, where controlled assembly and modification of peptide chains are critical. Its application extends to the development of peptide-based drugs, biomaterials, and probes for biochemical studies.
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