26537-88-2

Usage

Uses

Used in Industrial Solvents:
2-PERFLUOROPROPOXY-2,3,3,3-TETRAFLUOROPROPANOL is used as a solvent in various industrial processes due to its high non-flammability and thermal stability, making it suitable for heat-sensitive applications.
Used in Coating Production:
In the Coatings Industry, 2-PERFLUOROPROPOXY-2,3,3,3-TETRAFLUOROPROPANOL is used as a component in the production of coatings, leveraging its low surface tension and excellent wetting properties to enhance the performance and application of the coatings.
Used in Adhesive Formulation:
2-PERFLUOROPROPOXY-2,3,3,3-TETRAFLUOROPROPANOL is used as a component in adhesive formulations, where its wetting properties contribute to improved adhesion and bonding capabilities.
Used in Surfactant Manufacturing:
In the Surfactant Industry, 2-PERFLUOROPROPOXY-2,3,3,3-TETRAFLUOROPROPANOL is utilized in the manufacturing of surfactants, capitalizing on its properties to create products with superior performance in various applications.
Used in Semiconductor Industry:
2-PERFLUOROPROPOXY-2,3,3,3-TETRAFLUOROPROPANOL has potential applications in the semiconductor industry, where its unique properties may be employed in the manufacturing processes or as part of the materials used in semiconductor devices.
Used in Fluoropolymer Production:
2-PERFLUOROPROPOXY-2,3,3,3-TETRAFLUOROPROPANOL is used in the production of fluorinated polymers, contributing to the development of materials with enhanced properties such as chemical resistance and thermal stability.
It is crucial to handle 2-PERFLUOROPROPOXY-2,3,3,3-TETRAFLUOROPROPANOL with care, as it can pose risks to human health and the environment if not managed properly.

InChI:InChI=1/C6H3F11O2/c7-2(1-18,4(10,11)12)19-6(16,17)3(8,9)5(13,14)15/h18H,1H2

Upstream product

• 2062-98-8 perfluoro(2-propoxypropionyl) fluoride 
• 13140-34-6 methyl undecafluoro-2-methyl-3-oxahexanoate 

Relevant academic research and scientific papers

A 2 - full-fluorine third oxygen radical - 2, 3, 3, 3 - tetrafluoro propanol

The present invention provides a process for preparing 2 - full-fluorine third oxygen radical - 2, 3, 3, 3 - tetrafluoro propanol method, included in the non-proton solvent, selected from perfluoro - 2 - methyl - 3 - oxa - [...], full-fluoro - 2 - methyl - 3 - oxa - hexanoic acid methyl ester and perfluoro - 2 - methyl - 3 - oxa - caproate in at least one of raw materials, by sodium borohydride or potassium borohydride/obtained after the reduction. The present invention provides a preparation method, with high selectivity, high yield, low cost.

HYDROFLUOROOLEFINS AND METHODS OF USING SAME

A hydrofluoroolefin compound is represented by the following general formula (I): where Rf is a linear or branched perfluorinated alkyl group containing 2-10 carbon atoms and optionally contains (i) at least one catenated heteroatom selected from O or N; or (ii) a ring structure having 3 to 6 ring carbon atoms that optionally contains one or more catentated heteroatoms selected from O or N.

A method for preparing the fluorine carbon is mellow and its application (by machine translation)

The invention discloses a method for preparing the fluorine carbon is mellow and its application, the preparation method is with hexafluoropropylene oxide as the raw material, in a suitable reaction temperature, and under the action of the solvent in the catalyst, the polymerization of the generated or nexaituoropropene dimer and trimer, with no need for separate directly converted into a methyl ester, obtained by rectification of dimer, trimer methyl ester, the fluorine carbon is mellow respectively reduction of dimer, trimer the fluorine carbon is mellow, finally again rectification, the purity is as high as 99.7%. (by machine translation)

Fluorosurfactants

The present invention relates to novel compounds containing fluorinated end groups, to the use thereof as surface-active substances, and to compo-sitions comprising these compounds.

FLUOROSURFACTANTS

The present invention relates to novel compounds containing fluorinated end groups, to the use thereof as surface-active substances, and to compositions comprising these compounds.

PROCESS FOR PRODUCING FLUOROELASTOMERS

An emulsion polymerization process for the production of fluoroelastomers is disclosed wherein at least one fluorosurfactant is employed as dispersant, said fluorosurfactant being a fluoroalkylphosphoric acid ester of the formula X—Rf—(CH2)n—O—P(O)(OM)2, wherein n=1 or 2, X=H or F, M=a univalent cation, and Rf is a C4-C6 fluoroalkyl or fluoroalkoxy group. Optionally, a second dispersing agent may be employed in the polymerization, said second agent being a perfluoropolyether having at least one endgroup selected from the group consisting of carboxylic acid, a salt thereof, sulfonic acid and a salt thereof, phosphoric acid and a salt thereof.