N-(5-(2-Bromoacetamido)pentyl)acrylamide

95%

Reagent Code: #218340
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CAS Number 859161-71-0

science Other reagents with same CAS 859161-71-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 277.16 g/mol
Formula C₁₀H₁₇BrN₂O₂
badge Registry Numbers
MDL Number MFCD28977485
thermostat Physical Properties
Boiling Point 501.8±50.0 °C
inventory_2 Storage & Handling
Density 1.296±0.06 g/cm3
Storage 2-8°C

description Product Description

Used in the synthesis of functional polymers and hydrogels due to its dual reactivity. The acrylamide group participates in free radical polymerization, enabling incorporation into polymer networks, while the bromoacetamido group provides a site for nucleophilic substitution, allowing conjugation with thiols or amines. Commonly employed in bioconjugation strategies and the development of responsive materials for drug delivery or biosensing applications. Also utilized as a crosslinking agent in the preparation of affinity gels and immobilized biomolecules.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿14,980.00
inventory 100mg
10-20 days ฿25,000.00
inventory 250mg
10-20 days ฿44,000.00
inventory 1g
10-20 days ฿82,000.00

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N-(5-(2-Bromoacetamido)pentyl)acrylamide
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Used in the synthesis of functional polymers and hydrogels due to its dual reactivity. The acrylamide group participates in free radical polymerization, enabling incorporation into polymer networks, while the bromoacetamido group provides a site for nucleophilic substitution, allowing conjugation with thiols or amines. Commonly employed in bioconjugation strategies and the development of responsive materials for drug delivery or biosensing applications. Also utilized as a crosslinking agent in the prepar

Used in the synthesis of functional polymers and hydrogels due to its dual reactivity. The acrylamide group participates in free radical polymerization, enabling incorporation into polymer networks, while the bromoacetamido group provides a site for nucleophilic substitution, allowing conjugation with thiols or amines. Commonly employed in bioconjugation strategies and the development of responsive materials for drug delivery or biosensing applications. Also utilized as a crosslinking agent in the preparation of affinity gels and immobilized biomolecules.

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