Date published: 2025-10-15

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Pentafluorophenyl methacrylate (CAS 13642-97-2)

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Alternate Names:
Methacrylic acid
CAS Number:
13642-97-2
Purity:
95%
Molecular Weight:
252.14
Molecular Formula:
C10H5F5O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Pentafluorophenyl methacrylate (PFMA) is a highly utilized monomer in the polymer industry due to its exceptional properties, making it invaluable for various applications. These applications encompass the synthesis of polymers, adhesives, coatings, and elastomers. Beyond its significance in the aforementioned industries, Pentafluorophenyl methacrylate finds extensive use in crafting polymeric materials for biomedical purposes, including drug delivery systems and tissue engineering scaffolds.


Pentafluorophenyl methacrylate (CAS 13642-97-2) References

  1. Surface reactivity of pulsed-plasma polymerized pentafluorophenyl methacrylate (PFM) toward amines and proteins in solution.  |  Francesch, L., et al. 2007. Langmuir. 23: 3927-31. PMID: 17338554
  2. Immobilization of biomolecules to plasma polymerized pentafluorophenyl methacrylate.  |  Duque, L., et al. 2010. Biomacromolecules. 11: 2818-23. PMID: 20831201
  3. Efficient cell reprogramming using bioengineered surfaces.  |  Horna, D., et al. 2012. Adv Healthc Mater. 1: 177-82. PMID: 23184721
  4. Synthesis of maleimide-functionalyzed HPMA-copolymers and in vitro characterization of the aRAGE- and human immunoglobulin (huIgG)-polymer conjugates.  |  Tappertzhofen, K., et al. 2013. Macromol Biosci. 13: 203-14. PMID: 23239639
  5. Size-dependent knockdown potential of siRNA-loaded cationic nanohydrogel particles.  |  Nuhn, L., et al. 2014. Biomacromolecules. 15: 4111-21. PMID: 25338185
  6. Detection of Peptide-based nanoparticles in blood plasma by ELISA.  |  Bode, GH., et al. 2015. PLoS One. 10: e0126136. PMID: 25996618
  7. Pentafluorophenyl Ester-based Polymersomes as Nanosized Drug-Delivery Vehicles.  |  Scherer, M., et al. 2016. Macromol Rapid Commun. 37: 60-66. PMID: 26480295
  8. Novel grafted electrochemical interface for covalent glucose oxidase immobilization using reactive pentafluorophenyl methacrylate.  |  Artigues, M., et al. 2019. Colloids Surf B Biointerfaces. 175: 1-9. PMID: 30508760
  9. Copolymerization of Pentafluorophenylmethacrylate with Hydrophilic Methacrylamide Monomers Induces Premature Hydrolytic Cleavage.  |  Heraud, C., et al. 2019. Macromol Rapid Commun. 40: e1900278. PMID: 31328341
  10. Improving linking interface between collagen-based hydrogels and bone-like substrates.  |  Mas-Vinyals, A., et al. 2019. Colloids Surf B Biointerfaces. 181: 864-871. PMID: 31382334
  11. Synthesis and Postpolymerization Modification of Fluorine-End-Labeled Poly(Pentafluorophenyl Methacrylate) Obtained via RAFT Polymerization.  |  Battistella, C., et al. 2018. ACS Omega. 3: 9710-9721. PMID: 31459100
  12. Dual-reactive nanogels for orthogonal functionalization of hydrophilic shell and amphiphilic network.  |  Gruber, A., et al. 2022. Soft Matter. 18: 2858-2871. PMID: 35348179
  13. Backbone-Degradable Polymers via Radical Copolymerizations of Pentafluorophenyl Methacrylate with Cyclic Ketene Acetal: Pendant Modification and Efficient Degradation by Alternating-Rich Sequence.  |  Lai, H. and Ouchi, M. 2021. ACS Macro Lett. 10: 1223-1228. PMID: 35549050
  14. Post-Polymerization Modification of Fluoropolymers via UV Irradiation in the Presence of a Photoacid Generator.  |  Nika, A., et al. 2023. Polymers (Basel). 15: PMID: 36771794
  15. [Copolymerization of methyl methacrylate with pentafluorophenyl methacrylate and physical characteristics of the polymers (author's transl)].  |  Kadoma, Y. and Masuhara, E. 1981. Tokyo Ika Shika Daigaku Iyo Kizai Kenkyusho Hokoku. 15: 23-9. PMID: 6955907

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Pentafluorophenyl methacrylate, 1 g

sc-257983
1 g
$107.00