1H,1H,5H-Octafluoropentyl Acrylate
1H,1H,5H-Octafluoropentyl Acrylate Basic information
- Product Name:
- 1H,1H,5H-Octafluoropentyl Acrylate
- Synonyms:
-
- 1H,1H,5H-Octafluoropentyl
- Propenoic acid 2,2,3,3,4,4,5,5-octafluoropentyl ester
- Octafluoropentyl acrylate
- OFPA
- 1H,1H,5H-Octafluoropentyl Acrylate 
- 1H,1H,5H-Octafluoropentyl Acrylate (stabilized with MEHQ)
- 2,2,3,3,4,4,5,5-Octafluoropentyl acrylate, stabilized with &ap:50ppm 4-methoxyphenol
- DAIKIN R-5410
- CAS:
- 376-84-1
- MF:
- C8H6F8O2
- MW:
- 286.12
- EINECS:
- 206-816-5
- Product Categories:
-
- Monomers
- monomer
- Fluorous Chemistry
- Fluorous Compounds
- Synthetic Organic Chemistry
- Acrylic Monomers
- Fluorinated AcrylicsSelf Assembly&Contact Printing
- Fluorine-Containing Monomers for 157 nm UV Lithography Resist Polymers
- Lithography Monomers
- Mol File:
- 376-84-1.mol
1H,1H,5H-Octafluoropentyl Acrylate Chemical Properties
- Boiling point:
- 122 °C/140 mmHg (lit.)
- Density
- 1.488 g/mL at 25 °C (lit.)
- RTECS
- UD3643645
- refractive index
- n20/D 1.349(lit.)
- Flash point:
- 161 °F
- storage temp.
- 2-8°C
- Water Solubility
- Practically insoluble in water
- form
- clear liquid
- color
- Colorless to Almost colorless
- Specific Gravity
- 1.481
- InChIKey
- WISUNKZXQSKYMR-UHFFFAOYSA-N
- CAS DataBase Reference
- 376-84-1(CAS DataBase Reference)
- NIST Chemistry Reference
- 1h,1h,5h-Octafluoropentyl acrylate(376-84-1)
- EPA Substance Registry System
- 2-Propenoic acid, 2,2,3,3,4,4,5,5-octafluoropentyl ester (376-84-1)
Safety Information
- Hazard Codes
- Xi,N,F
- Risk Statements
- 36/37/38-51/53
- Safety Statements
- 26-28-61
- RIDADR
- UN 3077 9/PG 3
- WGK Germany
- 2
- Hazard Note
- Flammable/Keep Cold
- HazardClass
- KEEP COLD, FLAMMABLE
- HS Code
- 29161290
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
1H,1H,5H-Octafluoropentyl Acrylate Usage And Synthesis
Uses
1H,1H,5H-octafluoropentyl acrylate (OFPA) belongs to fluorinated acrylates having different fluoroalkyl chains. Two Y-shaped molecules, combining two dissimilar (hydrophilic and hydrophobic) units with a reactive triethoxysilane moiety, were synthesized by Koizumi et al. The synthesis involved a Michael addition reaction of (aminopropyl)triethoxysilane with 2-hydroxyethyl acrylate (HEA), followed by the addition of either 2,2,2-trifluoroethyl acrylate (TFEA) or 1H,1H,5H-octafluoropentyl acrylate (OFPA)[1].
References
[1] Ryo Koizumi . “Amphiphilic silsesquioxane nanoparticles by hydrolytic condensation of Y-shaped triethoxysilanes having hydroxyl and fluoroalkyl groups: Synthesis, self-assembly, and surface properties.” Polymer 110 (2017): Pages 260-272.
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