1-(9H-Fluoren-9-yl)-3-oxo-2,7,10,13-tetraoxa-4-azahexadecan-16-oic acid
97%
- Product Code: 63584
CAS:
867062-95-1
| Molecular Weight: | 443.490 g./mol | Molecular Formula: | C₂₄H₂₉NO₇ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in the field of bioconjugation and peptide synthesis. It serves as a versatile linker molecule, enabling the attachment of various functional groups to peptides or proteins. Its structure, featuring a fluorenyl group and multiple ether linkages, makes it particularly useful for creating stable and cleavable bonds in complex biomolecules. It is often employed in solid-phase peptide synthesis (SPPS) to facilitate the stepwise assembly of amino acids, ensuring high efficiency and purity of the final product. Additionally, its carboxylic acid group allows for further functionalization, making it valuable in the development of targeted drug delivery systems and diagnostic probes. Its applications extend to the study of protein interactions and the design of novel biomaterials.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White powder |
| PURITY | 97-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | £40.51 |
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| 1.000 | 10-20 days | £124.62 |
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1-(9H-Fluoren-9-yl)-3-oxo-2,7,10,13-tetraoxa-4-azahexadecan-16-oic acid
This chemical is primarily utilized in the field of bioconjugation and peptide synthesis. It serves as a versatile linker molecule, enabling the attachment of various functional groups to peptides or proteins. Its structure, featuring a fluorenyl group and multiple ether linkages, makes it particularly useful for creating stable and cleavable bonds in complex biomolecules. It is often employed in solid-phase peptide synthesis (SPPS) to facilitate the stepwise assembly of amino acids, ensuring high efficiency and purity of the final product. Additionally, its carboxylic acid group allows for further functionalization, making it valuable in the development of targeted drug delivery systems and diagnostic probes. Its applications extend to the study of protein interactions and the design of novel biomaterials.
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