60699-51-6

Basic information

• Product Name: 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
• Synonyms: 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;1-Hexadecanol, 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-nonacosafluoro-;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-Nonacosafluoro-1-hexadecanol;1,1,2,2-Tetrahydroperfluoro-1-hexadecanol;Einecs 262-382-7
• CAS NO: 60699-51-6
• Molecular Formula: C₁₆H₅F₂₉O
• Molecular Weight: 764.1639928
• EINECS: 262-382-7
• Product Categories: Organics
• Mol File: 60699-51-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 284.8°C at 760 mmHg
• Flash Point: 126°C
• Appearance: /
• Density: 1.702g/cm³
• Vapor Pressure: 0.000335mmHg at 25°C
• Refractive Index: 1.292
• CAS DataBase Reference: 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(CAS DataBase Reference)
• NIST Chemistry Reference: 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(60699-51-6)
• EPA Substance Registry System: 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(60699-51-6)

Safety Data

• Hazardous Substances Data: 60699-51-6(Hazardous Substances Data)

Usage

General Description

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 a chemical compound with the molecular formula C16F35H26O. It is a fluorinated alcohol that contains 16 carbon atoms, 35 fluorine atoms, 26 hydrogen atoms, and one oxygen atom. 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 in various industrial applications, including as a surfactant, lubricant, and in the manufacturing of specialized materials. It is known for its water-repellent properties and is often used in the production of non-stick coatings and water-resistant textiles. The large number of fluorine atoms in its structure gives it its unique properties and makes it useful for a wide range of applications.

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

• 116-14-3 polytetrafluoroethylene 
• 74-85-1 ethene 
• 354-64-3 Pentafluoroethyl iodide 
• 10192-85-5 potassium acrylate 
• 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 

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 articles and documents

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.

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.