4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(2-carboxyethyl)heptanedioic acid
95%
- Product Code: 52740
CAS:
798576-99-5
| Molecular Weight: | 469.48 g./mol | Molecular Formula: | C₂₅H₂₇NO₈ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16628194 | |
| Melting Point: | Boiling Point: | ||
| Density: | 1.352±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amino functionality, ensuring selective reactions during the peptide chain assembly. The presence of carboxylic acid groups allows for further conjugation or modification, making it a versatile building block in the creation of complex peptides. Its application is particularly significant in solid-phase peptide synthesis (SPPS), where it aids in the stepwise construction of peptides with high precision and efficiency. Additionally, it can be used in the development of peptide-based drugs, biomaterials, and research tools due to its stability and reactivity under controlled conditions.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | colourless to white |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,820.00 |
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| 0.250 | 10-20 days | ฿4,290.00 |
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4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(2-carboxyethyl)heptanedioic acid
This chemical is primarily utilized in peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amino functionality, ensuring selective reactions during the peptide chain assembly. The presence of carboxylic acid groups allows for further conjugation or modification, making it a versatile building block in the creation of complex peptides. Its application is particularly significant in solid-phase peptide synthesis (SPPS), where it aids in the stepwise construction of peptides with high precision and efficiency. Additionally, it can be used in the development of peptide-based drugs, biomaterials, and research tools due to its stability and reactivity under controlled conditions.
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