4,7,10,13,16,19-Hexaoxa-22-azapentacosanoic acid, 25-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)-23-oxo-, 2,5-dioxo-1-pyrrolidinyl ester
95%
- Product Code: 195982
CAS:
1137109-21-7
| Molecular Weight: | 601.60 g./mol | Molecular Formula: | C₂₆H₃₉N₃O₁₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11041093 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C |
Product Description:
Used primarily as a crosslinking agent in bioconjugation, this compound enables the stable attachment of biomolecules such as peptides, proteins, and antibodies to synthetic polymers or surfaces. Its activated ester group reacts efficiently with primary amines under mild aqueous conditions, forming stable amide bonds. The extended hydrophilic linker containing multiple oxygen atoms improves solubility in water and reduces nonspecific binding, making it ideal for applications in immunoassays, targeted drug delivery systems, and surface functionalization of medical devices. It is also employed in the preparation of protein microarrays and in the development of diagnostic probes where controlled orientation and minimal aggregation are critical.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿3,740.00 |
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| 250mg | 10-20 days | ฿5,880.00 |
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| 1g | 10-20 days | ฿22,700.00 |
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4,7,10,13,16,19-Hexaoxa-22-azapentacosanoic acid, 25-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)-23-oxo-, 2,5-dioxo-1-pyrrolidinyl ester
Used primarily as a crosslinking agent in bioconjugation, this compound enables the stable attachment of biomolecules such as peptides, proteins, and antibodies to synthetic polymers or surfaces. Its activated ester group reacts efficiently with primary amines under mild aqueous conditions, forming stable amide bonds. The extended hydrophilic linker containing multiple oxygen atoms improves solubility in water and reduces nonspecific binding, making it ideal for applications in immunoassays, targeted drug delivery systems, and surface functionalization of medical devices. It is also employed in the preparation of protein microarrays and in the development of diagnostic probes where controlled orientation and minimal aggregation are critical.
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