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%

Reagent Code: #195982
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CAS Number 1137109-21-7

science Other reagents with same CAS 1137109-21-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 601.60 g/mol
Formula C₂₆H₃₉N₃O₁₃
badge Registry Numbers
MDL Number MFCD11041093
inventory_2 Storage & Handling
Storage -20°C

description 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.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,740.00
inventory 250mg
10-20 days ฿5,880.00
inventory 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
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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 dru

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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