14-((2,5-Dioxopyrrolidin-1-yl)oxy)-14-oxotetradecanoic acid
95%
- Product Code: 40322
CAS:
146004-82-2
| Molecular Weight: | 355.4260 g./mol | Molecular Formula: | C₁₈H₂₉NO₆ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of bioconjugation and protein modification. It serves as a crosslinking agent, enabling the attachment of biomolecules, such as proteins or peptides, to other substrates or molecules. The reactive N-hydroxysuccinimide (NHS) ester group facilitates the formation of stable amide bonds with primary amines, making it valuable in the development of bioconjugates for research, diagnostics, and therapeutic applications. Additionally, it is employed in surface functionalization of materials, such as nanoparticles or polymers, to enhance their biocompatibility or targeting capabilities in drug delivery systems. Its long hydrocarbon chain provides flexibility and spacing, which can be beneficial in maintaining the functionality of conjugated biomolecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $294.73 |
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14-((2,5-Dioxopyrrolidin-1-yl)oxy)-14-oxotetradecanoic acid
This chemical is primarily utilized in the field of bioconjugation and protein modification. It serves as a crosslinking agent, enabling the attachment of biomolecules, such as proteins or peptides, to other substrates or molecules. The reactive N-hydroxysuccinimide (NHS) ester group facilitates the formation of stable amide bonds with primary amines, making it valuable in the development of bioconjugates for research, diagnostics, and therapeutic applications. Additionally, it is employed in surface functionalization of materials, such as nanoparticles or polymers, to enhance their biocompatibility or targeting capabilities in drug delivery systems. Its long hydrocarbon chain provides flexibility and spacing, which can be beneficial in maintaining the functionality of conjugated biomolecules.
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