(±)-trans-9,10-Epoxystearic Acid Methyl Ester

epoxy value~4

Reagent Code: #181882
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Alias Epoxy fatty acid methyl ester
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CAS Number 6084-76-0

science Other reagents with same CAS 6084-76-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 312.49 g/mol
Formula C₁₉H₃₆O₃
thermostat Physical Properties
Boiling Point 385.9 ºC at 760 mmHg
inventory_2 Storage & Handling
Density 0.925 g/cm3
Storage 2~8℃

description Product Description

Used as a key intermediate in the synthesis of specialty polymers and biodegradable plasticizers due to its reactive epoxide ring, which allows for cross-linking and chemical modification. Commonly employed in coatings, adhesives, and resins to improve flexibility, adhesion, and thermal stability. Also utilized in research for developing bio-based lubricants and surfactants, leveraging its natural origin and functional groups for sustainable material design. Its epoxide functionality enables ring-opening reactions to introduce hydroxyl or other polar groups, enhancing compatibility in composite materials.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿570.00
inventory 100g
10-20 days ฿1,550.00
inventory 500g
10-20 days ฿5,100.00
inventory 2.5kg
10-20 days ฿13,000.00

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(±)-trans-9,10-Epoxystearic Acid Methyl Ester
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Used as a key intermediate in the synthesis of specialty polymers and biodegradable plasticizers due to its reactive epoxide ring, which allows for cross-linking and chemical modification. Commonly employed in coatings, adhesives, and resins to improve flexibility, adhesion, and thermal stability. Also utilized in research for developing bio-based lubricants and surfactants, leveraging its natural origin and functional groups for sustainable material design. Its epoxide functionality enables ring-opening

Used as a key intermediate in the synthesis of specialty polymers and biodegradable plasticizers due to its reactive epoxide ring, which allows for cross-linking and chemical modification. Commonly employed in coatings, adhesives, and resins to improve flexibility, adhesion, and thermal stability. Also utilized in research for developing bio-based lubricants and surfactants, leveraging its natural origin and functional groups for sustainable material design. Its epoxide functionality enables ring-opening reactions to introduce hydroxyl or other polar groups, enhancing compatibility in composite materials.

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