2-Butene-1,4-diyl bis(bromoacetate)

90%

Reagent Code: #142394
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CAS Number 20679-58-7

science Other reagents with same CAS 20679-58-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 329.97 g/mol
Formula C₈H₁₀Br₂O₄
thermostat Physical Properties
Boiling Point 68℃(rough estimate)
inventory_2 Storage & Handling
Density 1.77g/ml
Storage Room temperature, dry

description Product Description

Used as a crosslinking agent in polymer chemistry, particularly in the synthesis of functionalized polymers and hydrogels. Its bifunctional ester groups react readily with nucleophiles such as amines or thiols, enabling the formation of covalent bonds between polymer chains. This property makes it valuable in creating networks for drug delivery systems, tissue engineering scaffolds, and responsive materials. It is also employed in organic synthesis to introduce bromoacetate functionalities for further derivatization. Due to its reactivity, it is handled with care in controlled environments.

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Test Parameter Specification
Appearance dark red to brown liquid
Purity 89.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 500g
10-20 days ฿4,980.00
inventory 2.5kg
10-20 days ฿16,500.00
inventory 10kg
10-20 days ฿52,800.00

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2-Butene-1,4-diyl bis(bromoacetate)
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Used as a crosslinking agent in polymer chemistry, particularly in the synthesis of functionalized polymers and hydrogels. Its bifunctional ester groups react readily with nucleophiles such as amines or thiols, enabling the formation of covalent bonds between polymer chains. This property makes it valuable in creating networks for drug delivery systems, tissue engineering scaffolds, and responsive materials. It is also employed in organic synthesis to introduce bromoacetate functionalities for further de

Used as a crosslinking agent in polymer chemistry, particularly in the synthesis of functionalized polymers and hydrogels. Its bifunctional ester groups react readily with nucleophiles such as amines or thiols, enabling the formation of covalent bonds between polymer chains. This property makes it valuable in creating networks for drug delivery systems, tissue engineering scaffolds, and responsive materials. It is also employed in organic synthesis to introduce bromoacetate functionalities for further derivatization. Due to its reactivity, it is handled with care in controlled environments.

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