26537-88-2

Basic information

• Product Name: 2-PERFLUOROPROPOXY-2,3,3,3-TETRAFLUOROPROPANOL
• Synonyms: 1H,1H-PERFLUORO(2-METHYL-3-OXAHEXAN-1-OL);2-HEPTAFLUOROPROPXY-2,3,3,3-TETRAFLUOROPROPAN-1-OL;2-HEPTAFLUOROPROPOXY-2,3,3,3-TETRAFLUOROPROPAN-1-OL;2-PERFLUOROPROPOXY-2,3,3,3-TETRAFLUOROPROPANOL;2-(Heptafluoropropxy)-2,3,3,3-tetrafluoropropan-1-ol 97%;2-(Heptafluoropropxy)-2,3,3,3-tetrafluoropropan-1-ol97%;1H,1H-Undecafluoro(2-methyl-3-oxahexan-1-ol) 97%;2-(Heptafluoropropxy)-2,3,3,3-tetrafluoropropan-1-ol, 1H,1H-Perfluoro(2-methyl-3-oxahexan-1-ol)
• CAS NO: 26537-88-2
• Molecular Formula: C₆H₃F₁₁O₂
• Molecular Weight: 316.07
• Mol File: 26537-88-2.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 115°C
• Flash Point: 88.6°C
• Appearance: /
• Density: 1.649g/cm³
• Vapor Pressure: 0.398mmHg at 25°C
• Refractive Index: 1.29
• Storage Temp.: Room Temperature, under inert atmosphere
• Solubility: Chloroform (Sparingly), Methanol (Slightly)
• PKA: 12.50±0.10(Predicted)
• CAS DataBase Reference: 2-PERFLUOROPROPOXY-2,3,3,3-TETRAFLUOROPROPANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PERFLUOROPROPOXY-2,3,3,3-TETRAFLUOROPROPANOL(26537-88-2)
• EPA Substance Registry System: 2-PERFLUOROPROPOXY-2,3,3,3-TETRAFLUOROPROPANOL(26537-88-2)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• Hazardous Substances Data: 26537-88-2(Hazardous Substances Data)

Usage

General Description

2-PERFLUOROPROPOXY-2,3,3,3-TETRAFLUOROPROPANOL is a fluorinated chemical compound that contains four fluorine atoms and a propoxy group. It is a colorless liquid with a strong odor, and it is commonly used as a solvent in industrial processes. This chemical is known for its high non-flammability and thermal stability, making it suitable for use in heat sensitive applications. It also has low surface tension and excellent wetting properties, which makes it useful in the production of coatings, adhesives, and surfactants. Additionally, 2-PERFLUOROPROPOXY-2,3,3,3-TETRAFLUOROPROPANOL has potential applications in the semiconductor industry and in the production of fluorinated polymers. However, it is important to handle this chemical with caution, as it can be hazardous to human health and the environment if not properly managed.

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

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

Relevant articles and documents

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.

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 compositions comprising these compounds.