19932-27-5

Usage

Uses

Used in Electronics Industry:
3-(1H,1H,5H-OCTAFLUOROPENTYLOXY)-1,2-EPOXYPROPANE is used as a solvent for its high thermal stability and chemical resistance, which are crucial for various electronic manufacturing processes.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 3-(1H,1H,5H-OCTAFLUOROPENTYLOXY)-1,2-EPOXYPROPANE serves as a heat transfer fluid, leveraging its thermal stability to maintain controlled temperatures in pharmaceutical manufacturing processes.
Used as a Lubricant:
3-(1H,1H,5H-OCTAFLUOROPENTYLOXY)-1,2-EPOXYPROPANE is utilized as a lubricant in various applications due to its low surface energy, which reduces friction and wear in mechanical systems.
Used in Manufacturing Processes:
3-(1H,1H,5H-OCTAFLUOROPENTYLOXY)-1,2-EPOXYPROPANE is employed in manufacturing as a heat transfer fluid, taking advantage of its ability to maintain stable temperatures and resist chemical reactions, which is essential for the production of various goods.
Given its low toxicity and relative safety, 3-(1H,1H,5H-OCTAFLUOROPENTYLOXY)-1,2-EPOXYPROPANE is a preferred choice for diverse industrial applications where chemical stability and safety are paramount.

Upstream product

• 355-80-6 2,2,3,3,4,4,5,5-octafluoropentan-1-ol 
• 106-89-8 epichlorohydrin 

Downstream Products

• 355-80-6 2,2,3,3,4,4,5,5-octafluoropentan-1-ol 
• 3108-07-4 3-(2,2,3,3,4,4,5,5-octafluoropentyloxy)-1-propene 

Relevant academic research and scientific papers

Thermal desulfurization of (Alkoxymethyl)thiiranes

Reaction of (alkoxymethyl)oxiranes with thiourea in methanol has afforded the corresponding thiiranes, and catalyst-free thermal desulfurization of the products has been studied. The major products of desulfurization are alcohols and alkenes, both in the cases of (polyfluoroalkyloxymethyl)thiiranes and their non-fluorinated analogs. Longer alkyl chain in thiiranes favors formation of alcohols over alkenes formation in the course of desulfurization.

Promising prospects for using partially fluorinated alcohols as O-nucleophilic reagents in organofluoric synthesis

Perfluoroolefins react with isopropyl alcohol under the conditions of radical initiation to form partially fluorinated aliphatic alcohols. The reactions of these alcohols with hexafluoropropylene and compounds containing labile halogen atoms (in particular, with allyl bromide and epichlorohydrin) were studied.

FLUORINE-CONTAINING 2,3-EPOXYPROPYL ETHERS. SYNTHESIS AND SPECTRAL CHARACTERISTICS

Polyfluoroalkyl 2,3-epoxypropyl ethers were prepared by the reactions of fluoro olefins with 2,3-epoxy-1-propanol in presence of potassium fluoride and under the conditions of phase-transfer catalysis. 1H and 19F NMR- and mass-spectral characteristics of the polyfluoroalkyl ethers were determined.