3-Perfluorooctyl-1,2-epoxypropane

99%

Reagent Code: #222579
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CAS Number 38565-53-6

science Other reagents with same CAS 38565-53-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 476.13 g/mol
Formula C₁₁H₅F₁₇O
badge Registry Numbers
EC Number 254-006-5
MDL Number MFCD00042362
thermostat Physical Properties
Melting Point 76-78 °C
Boiling Point 87 °C/19 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.712 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used primarily as a fluorinated building block in organic synthesis, this compound enables the introduction of highly fluorinated alkyl chains into larger molecules. Its epoxy functionality allows for ring-opening reactions, making it valuable in the development of specialty surfactants, water- and oil-repellent coatings, and surface modifiers for polymers. It is also employed in the synthesis of fluorinated intermediates for pharmaceuticals, agrochemicals, and advanced materials where thermal stability, chemical resistance, and low surface energy are required. Due to the long perfluorinated tail, it imparts strong hydrophobic and lipophobic characteristics to modified surfaces, useful in coatings for textiles, electronics, and medical devices.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿560.00
inventory 5g
10-20 days ฿1,640.00
inventory 25g
10-20 days ฿5,730.00
3-Perfluorooctyl-1,2-epoxypropane
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Used primarily as a fluorinated building block in organic synthesis, this compound enables the introduction of highly fluorinated alkyl chains into larger molecules. Its epoxy functionality allows for ring-opening reactions, making it valuable in the development of specialty surfactants, water- and oil-repellent coatings, and surface modifiers for polymers. It is also employed in the synthesis of fluorinated intermediates for pharmaceuticals, agrochemicals, and advanced materials where thermal stability,

Used primarily as a fluorinated building block in organic synthesis, this compound enables the introduction of highly fluorinated alkyl chains into larger molecules. Its epoxy functionality allows for ring-opening reactions, making it valuable in the development of specialty surfactants, water- and oil-repellent coatings, and surface modifiers for polymers. It is also employed in the synthesis of fluorinated intermediates for pharmaceuticals, agrochemicals, and advanced materials where thermal stability, chemical resistance, and low surface energy are required. Due to the long perfluorinated tail, it imparts strong hydrophobic and lipophobic characteristics to modified surfaces, useful in coatings for textiles, electronics, and medical devices.

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