Diethyl maleate

96%

  • Product Code: 169301
  Alias:    Diethyl maleate; diethyl maleate, dehydrated ethyl malate
  CAS:    141-05-9
Molecular Weight: 172.18 g./mol Molecular Formula: C₈H₁₂O₄
EC Number: 205-451-9 MDL Number: MFCD00009191
Melting Point: −10 °C(lit.) Boiling Point: 225 °C(lit.)
Density: 1.064 g/mL at 25 °C(lit.) Storage Condition: Room temperature
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.
Product Specification:
Test Specification
Purity (GC) 96-100
REFRACTIVE INDEX N20/D 1.439-1.443
SPECIFIC GRAVITY (20/20 Degree Celsius) 1.067-1.071
Water by Karl Fischer 0-0.2
APPEARANCE COLORLESS LIQUID
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size Availability Price Quantity
100ml 10-20 days ฿300.00
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250ml 10-20 days ฿610.00
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500ml 10-20 days ฿990.00
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10L 10-20 days ฿14,060.00
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-
12X500ml 10-20 days ฿11,760.00
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2.5L 10-20 days ฿4,360.00
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Diethyl maleate
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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