2-(Perfluorobutyl)ethyl acrylate

• Catalog Number: ACM52591272
• Product Name: 2-(Perfluorobutyl)ethyl acrylate
• CAS: 52591-27-2
• Category: Heterocyclic Organic Compound
• Description: 2-(Perfluorobutyl)ethyl acrylate (2-PFB-EAc) is a synthetic fluorinated monomer that is characterized by its low surface tension and high chemical stability.
• Synonyms: DAIKIN R-1420;1H,1H,2H,2H-Nonafluorohexyl acrylate;2-(Perfluorobutyl)ethyl acrylate;2-Propenoic acid 3,3,4,4,5,5,6,6,6-nonafluorohexyl ester;3,3,4,4,5,5,6,6,6-Nonafluorohexyl acrylate;3,3,4,4,5,5,6,6,6-Nonafluorohexylacrylate;Acrylic acid 2-(nonafluorobu
• Molecular Weight: 318.14
• Molecular Formula: C9H7F9O2
• Canonical SMILES: C=CC(=O)OCCC(C(C(C(F)(F)F)(F)F)(F)F)(F)F
• InChI: InChI=1S/C9H7F9O2/c1-2-5(19)20-4-3-6(10,11)7(12,13)8(14,15)9(16,17)18/h2H,1,3-4H2
• InChI Key: GYUPEJSTJSFVRR-UHFFFAOYSA-N
• Boiling Point: 164ºC
• Flash Point: 52ºC
• Density: 1.414 g/mL
• Application: 2-(Perfluorobutyl)ethyl acrylate has been used in a wide range of scientific research applications. It has been used to create polymers for biomedical applications, such as drug delivery systems and tissue engineering scaffolds. It has also been used to create polymers for industrial applications, such as coatings and adhesives. In addition, it has been used to create polymers for energy applications, such as fuel cells and solar cells.
• Storage: Store at 2-8 ℃
• Exact Mass: 318.03
• Features And Benefits: Its low surface tension makes it a desirable choice for the production of polymers with improved surface properties, while its high chemical stability makes it an ideal choice for biomedical research.
• HTS Code: 2916129000
• PSA: 26.3
• Refractive Index: 1.31
• XLogP3: 3.5739

Case Study

Synthesis of a new adsorbent based on 2-(Perfluorobutyl)ethyl acrylate and its application in the determination of perfluoroalkanesulfonamide (PFASA)

Yanmei Huang, et al. Talanta. 2019 Jan 15;192:24-31.

To extract perfluoroalkane sulfonamides (PFASAs) in water and urine samples effectively, a new adsorbent was synthesized and used as the extraction phase of multiple monolithic fiber solid-phase microextraction (MMF-SPME).
1H,1H,2H,2H-nonafluorohexyl acrylate (NF) and vinyboronic anhydride pyridine complex (VB) were selected as dual functional monomers to in-situ copolymerize with ethylenedimethacrylate (ED) to synthesize a new monolithic adsorbent (FBE) and used as the extraction phase of MMF-SPME (FBE/MMFSPME).