39239-79-7

Basic information

• Product Name: 1H,1H,2H,2H,3H,3H,4H,4H-Perfluorodecan-1-ol
• Synonyms: 1H,1H,2H,2H,3H,3H,4H,4H-Perfluorodecan-1-ol
• CAS NO: 39239-79-7
• Molecular Formula: C₁₀H₉F₁₃O
• Molecular Weight: 392.1571016
• Mol File: 39239-79-7.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H,1H,2H,2H,3H,3H,4H,4H-Perfluorodecan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1H,1H,2H,2H,3H,3H,4H,4H-Perfluorodecan-1-ol(39239-79-7)
• EPA Substance Registry System: 1H,1H,2H,2H,3H,3H,4H,4H-Perfluorodecan-1-ol(39239-79-7)

Safety Data

• Hazard Codes: F
• Hazardous Substances Data: 39239-79-7(Hazardous Substances Data)

Usage

Type of compound

Perfluorinated alcohol

Hydrogen atoms

Replaced with fluorine atoms

Physical state

Colorless liquid

Boiling point

High

Solubility

Insoluble in water

Applications

a. Surfactant in industrial applications
b. Production of fluorinated products (lubricants and coatings)
c. Building block for synthesis of other fluorinated compounds

Stability

Resistant to heat, chemicals, and environmental factors

Industrial processes

Valued component due to its stability and resistance properties

Upstream product

• 16083-68-4 5,5,6,6,7,7,8,8,9,9,10,10,10-tridecafluoro-3-iodo-decan-1-ol 
• 2043-57-4 1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-8-iodooctane 
• 25664-41-9 Diethyl tridecylfluoro-octyl-malonat 
• 26564-96-5 2-<2-(Perfluorhexyl)ethyl>-malonsaeure 
• 355-43-1 n-perfluorohexyl iodide 
• 27854-28-0 5,5,6,6,7,7,8,8,9,9,10,10,10-Tridecafluoro-dec-1-ene 
• 26564-97-6 5,5,6,6,7,7,8,8,9,9,10,10,10-Tridecafluoro-decanoic acid 
• 242473-86-5 5,5,6,6,7,7,8,8,9,9,10,10,10-tridecafluoro-decanoic acid ethyl ester 

Downstream Products

• 886575-48-0 3,4-bis-(5,5,6,6,7,7,8,8,9,9,10,10,10-tridecafluoro-decyloxy)-benzaldehyde 
• 946124-80-7 3,5-bis(1H,1H,2H,2H,3H,3H,4H,4H-perfluorodecan-1-yloxy)benzyl bromide 
• 946124-78-3 3,5-bis(1H,1H,2H,2H,3H,3H,4H,4H-perfluorodecan-1-yloxy)benzyl alcohol 
• 134440-52-1 tridecafluorodecyl 4-methylbenzenesulfonate 

Relevant articles and documents

Fabrication of self-assembled dendron monolayers

A dendron (2) comprising a focal point (4) and a plurality of fluorinated end groups (9) is disclosed, including one having a thiol, a silane, a carboxylic acid, a phosphonate or another moiety at the focal point suitable for chemisorption to a substrate

Synthesis and mesomorphism of fluoroalkylated organometallic mesogens

The first examples of liquid crystalline chloro-bridged dinuclear palladium organyls carrying semiperfluorinated alkyl chains at their peripheries have been synthesised. The liquid crystalline properties were investigated using polarised optical microscop

Convenient synthesis of thiols and disulfides in the polyfluorinated series incorporating a butylic spacer

New fluorinated thiols R(F)(CH2)(p)SH and disulfides [R(F)(CH2)(p)S]2 containing a butylic spacer (p=4) between the perfluorinated part and the thiol (or disulfide) function were easily obtained in good yields with a purity higher than 98%. This allows us to obtain homologues (p>4) for their use as synthetic intermediates or as constituents for molecular organized systems. (C) 2000 Elsevier Science Ltd.