Bis(2,5-dioxopyrrolidin-1-yl) 16-(3-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)propanoyl)-4,7,10,13,19,22,25,28-octaoxa-16-azahentriacontane-1,31-dioate
95%
- Product Code: 64763
CAS:
2112738-60-8
| Molecular Weight: | 858.84 g./mol | Molecular Formula: | C₃₇H₅₄N₄O₁₉ |
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| EC Number: | MDL Number: | MFCD29912654 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
This chemical is primarily utilized as a versatile crosslinking agent in the development of advanced polymeric materials. Its structure, featuring multiple reactive sites, allows it to form strong covalent bonds with various functional groups, making it particularly effective in creating stable, high-performance polymers. It is often employed in the synthesis of hydrogels, which are widely used in biomedical applications such as drug delivery systems, tissue engineering scaffolds, and wound dressings. Additionally, its ability to crosslink proteins and peptides makes it valuable in bioconjugation processes, enabling the modification of biomolecules for therapeutic or diagnostic purposes. The compound’s water-soluble nature further enhances its utility in aqueous-based formulations, ensuring compatibility with biological systems.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $4,475.14 |
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Bis(2,5-dioxopyrrolidin-1-yl) 16-(3-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)propanoyl)-4,7,10,13,19,22,25,28-octaoxa-16-azahentriacontane-1,31-dioate
This chemical is primarily utilized as a versatile crosslinking agent in the development of advanced polymeric materials. Its structure, featuring multiple reactive sites, allows it to form strong covalent bonds with various functional groups, making it particularly effective in creating stable, high-performance polymers. It is often employed in the synthesis of hydrogels, which are widely used in biomedical applications such as drug delivery systems, tissue engineering scaffolds, and wound dressings. Additionally, its ability to crosslink proteins and peptides makes it valuable in bioconjugation processes, enabling the modification of biomolecules for therapeutic or diagnostic purposes. The compound’s water-soluble nature further enhances its utility in aqueous-based formulations, ensuring compatibility with biological systems.
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