120464-27-9

Basic information

• Product Name: 1-(PERFLUOROHEXYL)DEC-1-ENE
• Synonyms: 1-(perfluoro-n-hexyl)-decene-1;1,1,1,2,2,3,3,4,4,5,5,6,6-TRIDECAFLUORO-7-HEXADECENE;1-PERFLUOROHEXYL-1-DECENE;1-(PERFLUOROHEXYL)DEC-1-ENE
• CAS NO: 120464-27-9
• Molecular Formula: C₁₆H₁₉F₁₃
• Molecular Weight: 458.3
• Mol File: 120464-27-9.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 276.6±8.0 °C(Predicted)
• Appearance: /
• Density: 1.282±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1-(PERFLUOROHEXYL)DEC-1-ENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(PERFLUOROHEXYL)DEC-1-ENE(120464-27-9)
• EPA Substance Registry System: 1-(PERFLUOROHEXYL)DEC-1-ENE(120464-27-9)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 120464-27-9(Hazardous Substances Data)

Usage

Type of Compound

Fluorinated compound

Industrial Applications

Surface coatings
Lubricants
Polymers

Properties

Surfactant
Wetting agent
Heat resistance
Chemical resistance
Surface tension resistance

Uses

Water-repellent surfaces
Non-stick surfaces
Electronics manufacturing
Textiles production
Paper products

Environmental Impact

Low toxicity and environmental impact

Health Considerations

Care should be taken when handling and using PFHD-1 due to potential harmful effects on human health and the environment.

Upstream product

• 764-93-2 1-decyne 
• 355-43-1 n-perfluorohexyl iodide 
• 355-41-9 perfluoro-n-hexyl chloride 
• 335-56-8 1-bromo-1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane 

Relevant articles and documents

Metal-Free Visible-Light Radical Iodoperfluoroalkylation of Terminal Alkenes and Alkynes

The organic-dye-catalyzed visible-light-induced iodoperfluoroalkylation of unactivated terminal alkenes and alkynes was explored. This process was found to be effective for the simultaneous introduction of iodide and various perfluoroalkyl groups (including difluoroacetate) to alkenes and alkynes possessing a variety of functional groups. A possible reaction mechanism is proposed. This reaction provides a new, metal-free, green method for the synthesis of perfluoroalkylated compounds.

Nickel(0)-catalyzed fluoroalkylation of alkenes, alkynes, and aromatics with perfluoroalkyl chlorides

Treatment of perfluoroalkyl chlorides (RFCl) with alkenes, alkynes, or aromatics in the presence of 0.1 equiv of nickel dichloride, 1.5 equiv of zinc powder, and 0.4 equiv of triphenylphosphine in DMF at 95-100 °C for 6-8 h give the correspondi