FMOC-1-AMINO-4,7,10-TRIOXA-13-TRIDECANAMINE SUCCINIMIC ACID
95% (HPLC)
- Product Code: 188348
CAS:
172089-14-4
| Molecular Weight: | 542.62 g./mol | Molecular Formula: | C₂₉H₃₈N₂O₈ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD05663769 | |
| Melting Point: | Boiling Point: | 792.0±60.0 °C(Predicted) | |
| Density: | 1.208±0.06 g/cm3(Predicted) | Storage Condition: | -20°C |
Product Description:
Used primarily in peptide synthesis, this reagent serves as a building block for introducing a hydrophilic, flexible linker with a terminal amine protected by the FMOC group. The polyether chain enhances solubility in aqueous and organic solvents, making it valuable in the development of peptide-based drugs, bioconjugates, and functionalized polymers. After deprotection of the FMOC group, the exposed amine allows for further coupling with carboxylic acids or other electrophiles. Its structure is particularly useful in solid-phase synthesis and in the preparation of PEG-like spacers to reduce aggregation and improve bioavailability. Commonly applied in medicinal chemistry and biochemical research for constructing complex molecular architectures.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿9,340.00 |
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FMOC-1-AMINO-4,7,10-TRIOXA-13-TRIDECANAMINE SUCCINIMIC ACID
Used primarily in peptide synthesis, this reagent serves as a building block for introducing a hydrophilic, flexible linker with a terminal amine protected by the FMOC group. The polyether chain enhances solubility in aqueous and organic solvents, making it valuable in the development of peptide-based drugs, bioconjugates, and functionalized polymers. After deprotection of the FMOC group, the exposed amine allows for further coupling with carboxylic acids or other electrophiles. Its structure is particularly useful in solid-phase synthesis and in the preparation of PEG-like spacers to reduce aggregation and improve bioavailability. Commonly applied in medicinal chemistry and biochemical research for constructing complex molecular architectures.
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