60699-51-6

Usage

Uses

Used in Surfactant Applications:
3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,14,14,15,15,16,16,16-nonacosafluorohexadecanol is used as a surfactant in various industrial processes. Its water-repellent properties make it suitable for creating formulations that reduce the surface tension of liquids, enhancing the spreading and wetting of substances.
Used in Lubricant Applications:
In the lubricant industry, 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,14,14,15,15,16,16,16-nonacosafluorohexadecanol serves as a lubricant due to its ability to reduce friction between surfaces. Its fluorinated nature provides it with a low coefficient of friction, making it an effective component in lubricating formulations.
Used in Manufacturing of Specialized Materials:
3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,14,14,15,15,16,16,16-nonacosafluorohexadecanol is utilized in the production of specialized materials that require unique properties such as non-stick surfaces or water and oil repellency. Its fluorinated structure imparts these characteristics to the materials, making it valuable in various applications.
Used in Non-stick Coating Industry:
3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,14,14,15,15,16,16,16-nonacosafluorohexadecanol is used as a key component in the formulation of non-stick coatings for cookware and other surfaces. Its water-repellent and low-adhesion properties contribute to the effectiveness of these coatings.
Used in Water-resistant Textile Industry:
In the textile industry, 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,14,14,15,15,16,16,16-nonacosafluorohexadecanol is employed to create water-resistant fabrics. Its fluorinated structure allows for the development of textiles that repel water, making them suitable for outdoor and performance wear.

InChI:InChI=1/C16H5F29O/c17-3(18,1-2-46)4(19,20)5(21,22)6(23,24)7(25,26)8(27,28)9(29,30)10(31,32)11(33,34)12(35,36)13(37,38)14(39,40)15(41,42)16(43,44)45/h46H,1-2H2

Upstream product

• 65510-55-6 1-iodo-1H,1H,2H,2H-perfluorohexadecane 
• 2043-55-2 3,3,4,4,5,5,6,6,6-nonafluorohexyliodide 
• 2043-57-4 1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-8-iodooctane 
• 2043-53-0 2-(n-perfluorooctyl)ethyl iodide 
• 2043-54-1 1-iodo-1H,1H,2H,2H-perfluorododecane 
• 30046-31-2 1-iodo-1H,1H,2H,2H-perfluorotetradecane 
• 116-14-3 polytetrafluoroethylene 
• 74-85-1 ethene 
• 354-64-3 Pentafluoroethyl iodide 
• 10192-85-5 potassium acrylate 

Downstream Products

• 34395-24-9 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,14,14,14-pentacosafluoro-tetradecyl acrylate 
• 34362-49-7 C₁₄F₂₉CH₂CH₂OCOCH=CH₂ 
• 27905-45-9 1H,1H,2H,2H-heptadecafluorodecyl acrylate 
• 17741-60-5 1,1,2,2-Tetrahydroperfluorododecyl acrylate 

Relevant academic research and scientific papers

PROCESS FOR PRODUCING FLUORINATED (METH)ACRYLIC ESTER

A mixture of fluoroalkyl iodides of the formula C2F5(CF2CF2)nI ( n is an integer of ≥0) wherein the sum of such fluoroalkyl iodides of n=3 and n=4 contained is ≥85 mol% is provided. This mixture is subjected to an ethylene addition step and an esterification step, and C2F5(CF2CF2)nCH=CH2 and C2F5(CF2CF2)nCH2CH2OH are removed. Thus, there can be obtained a mixture of fluorine-containing (meth)acrylic esters of the formula C2F5(CF2CF2)nCH2CH2OCOCR1=CH2 (wherein R1 represents a hydrogen atom or a methyl group, and n is an integer of ≥0) wherein the content of impurities (namely, olefins of the formula C2F5(CF2CF2)nCH=CH2 and alcohols of the formula C2F5(CF2CF2)nCH2CH2OH) is low.

Purification of fluorinated alcohols

A process for reducing the level of perfluoroalkanoic acids, perfluoroalkanoic esters, and perfluoroalkyliodides in fluorinated alcohols comprising heating a fluorinated alcohol, or mixtures thereof, containing said acids, esters, or iodides to a temperature of at least 175° C. in the presence of water and a base additive is disclosed.

Catalysts for the preparation of fluorinated alcohols and process for the preparation of fluorinated alcohols

The present invention provides a catalyst for preparing a fluorine-containing alcohol compound, the catalyst having at least one component selected from elements in Group 1B, Group 2B, Group 6A, Group 7A and Group 8 of the periodic table, ions of these elements, oxides containing these elements, hydroxides containing these elements and salts containing these elements, said component being supported on at least one complex oxide selected from Si—Al complex oxides, Al—P complex oxides and Si—Al—P complex oxides; and a method for preparing a fluorine-containing alcohol compound, the method comprising reacting a halogenated fluorine compound with water in the presence of the catalyst. According to the present invention, a fluorine-containing alcohol compound can be prepared at a relatively low reaction temperature and in a high yield.