Fmoc-Gly-Gly-Gly-OH
97%
- Product Code: 54984
CAS:
170941-79-4
Molecular Weight: | 411.41 g./mol | Molecular Formula: | C₂₁H₂₁N₃O₆ |
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EC Number: | MDL Number: | MFCD00190881 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This tripeptide derivative is commonly used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). The Fmoc (fluorenylmethyloxycarbonyl) protecting group is crucial for temporarily shielding the amino group during the assembly of peptide chains, allowing for selective deprotection and elongation. Its application is widespread in the production of custom peptides for research, pharmaceuticals, and biotechnology. It serves as a building block for creating complex peptide structures, enabling the study of protein interactions, drug development, and the design of bioactive compounds. Additionally, it is utilized in the development of peptide-based therapeutics, diagnostics, and biomaterials due to its stability and compatibility with automated synthesis techniques.
Product Specification:
Test | Specification |
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APPEARANCE | solid |
PURITY | 96.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | $22.07 |
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1.000 | 10-20 days | $53.54 |
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5.000 | 10-20 days | $192.55 |
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10.000 | 10-20 days | $375.24 |
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Fmoc-Gly-Gly-Gly-OH
This tripeptide derivative is commonly used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). The Fmoc (fluorenylmethyloxycarbonyl) protecting group is crucial for temporarily shielding the amino group during the assembly of peptide chains, allowing for selective deprotection and elongation. Its application is widespread in the production of custom peptides for research, pharmaceuticals, and biotechnology. It serves as a building block for creating complex peptide structures, enabling the study of protein interactions, drug development, and the design of bioactive compounds. Additionally, it is utilized in the development of peptide-based therapeutics, diagnostics, and biomaterials due to its stability and compatibility with automated synthesis techniques.
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