1,2-Epoxyoctane

97%

Reagent Code: #181739
label
Alias 1,2-epoxyoctane;octene oxide
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CAS Number 2984-50-1

science Other reagents with same CAS 2984-50-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 128.21 g/mol
Formula C₈H₁₆O
badge Registry Numbers
EC Number 221-047-5
MDL Number MFCD00005157
thermostat Physical Properties
Boiling Point 62-64 °C17 mm Hg(lit.)
inventory_2 Storage & Handling
Density 0.835 g/mL at 20 °C(lit.)
Storage 2~8°C, dry

description Product Description

Used as a reactive diluent in epoxy resin systems, improving processability and flexibility of coatings, adhesives, and composites. Acts as an intermediate in the synthesis of surfactants, lubricants, and specialty chemicals due to its ability to undergo ring-opening reactions with nucleophiles such as amines, alcohols, and acids. Employed in the preparation of polyether polyols for polyurethane formulations, contributing to tailored mechanical and thermal properties. Also utilized in research for modifying polymer architectures and surface functionalization.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿310.00
inventory 5g
10-20 days ฿820.00
inventory 25g
10-20 days ฿3,320.00
inventory 100g
10-20 days ฿11,210.00

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1,2-Epoxyoctane
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Used as a reactive diluent in epoxy resin systems, improving processability and flexibility of coatings, adhesives, and composites. Acts as an intermediate in the synthesis of surfactants, lubricants, and specialty chemicals due to its ability to undergo ring-opening reactions with nucleophiles such as amines, alcohols, and acids. Employed in the preparation of polyether polyols for polyurethane formulations, contributing to tailored mechanical and thermal properties. Also utilized in research for modify

Used as a reactive diluent in epoxy resin systems, improving processability and flexibility of coatings, adhesives, and composites. Acts as an intermediate in the synthesis of surfactants, lubricants, and specialty chemicals due to its ability to undergo ring-opening reactions with nucleophiles such as amines, alcohols, and acids. Employed in the preparation of polyether polyols for polyurethane formulations, contributing to tailored mechanical and thermal properties. Also utilized in research for modifying polymer architectures and surface functionalization.

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