Diethyl maleate

96%

Reagent Code: #169301
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Alias Diethyl maleate; diethyl maleate, dehydrated ethyl malate
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CAS Number 141-05-9

science Other reagents with same CAS 141-05-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.18 g/mol
Formula C₈H₁₂O₄
badge Registry Numbers
EC Number 205-451-9
MDL Number MFCD00009191
thermostat Physical Properties
Melting Point −10 °C(lit.)
Boiling Point 225 °C(lit.)
inventory_2 Storage & Handling
Density 1.064 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as a reactive diluent and crosslinking agent in polymer formulations, particularly in unsaturated polyester resins and coatings. Enhances curing efficiency and improves the mechanical and thermal properties of the final product. Employed in the synthesis of specialty monomers and copolymers due to its ability to undergo Michael addition and free radical polymerization. Also utilized in the development of adhesives and sealants where low viscosity and good reactivity are required. Acts as a building block in organic synthesis for pharmaceuticals and agrochemicals, leveraging its electron-deficient double bond for nucleophilic attack.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (GC) 96-100
Refractive Index (N20/D) 1.439-1.443
Specific Gravity (20/20°C) 1.067-1.071
Water (Karl Fischer) 0-0.2
Appearance Colorless liquid
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100ml
10-20 days ฿300.00
inventory 250ml
10-20 days ฿610.00
inventory 500ml
10-20 days ฿990.00
inventory 10L
10-20 days ฿14,060.00
inventory 12X500ml
10-20 days ฿11,760.00
inventory 2.5L
10-20 days ฿4,360.00

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Diethyl maleate
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Used as a reactive diluent and crosslinking agent in polymer formulations, particularly in unsaturated polyester resins and coatings. Enhances curing efficiency and improves the mechanical and thermal properties of the final product. Employed in the synthesis of specialty monomers and copolymers due to its ability to undergo Michael addition and free radical polymerization. Also utilized in the development of adhesives and sealants where low viscosity and good reactivity are required. Acts as a building block in organic synthesis for pharmaceuticals and agrochemicals, leveraging its electron-deficient double bond for nucleophilic attack.
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