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3-(Perfluorooctyl)-1,2-propenoxide (CAS 38565-53-6)

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Alternate Names:
(2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,9-Heptadecafluorononyl)oxirane
Application:
3-(Perfluorooctyl)-1,2-propenoxide is a fluorinated epoxide with antibacterial properties
CAS Number:
38565-53-6
Molecular Weight:
476.13
Molecular Formula:
C11H5F17O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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3-(Perfluorooctyl)-1,2-propenoxide, also referred to as PFO, is a versatile perfluorinated compound widely employed in scientific research and technological fields. Renowned for its exceptional stability and solubility in both organic and inorganic solvents, 3-(Perfluorooctyl)-1,2-propenoxide finds applications in an array of domains, encompassing polymer production, medical advancements, and laboratory product development. Within scientific research, 3-(Perfluorooctyl)-1,2-propenoxide plays multiple roles. It acts as a surfactant in polymer manufacturing and enhances lubrication during laboratory experiments. Additionally, its utilization extends to the creation of medical devices like catheters and endoscopes. The inherent stability of 3-(Perfluorooctyl)-1,2-propenoxide stems from the presence of the perfluoroalkyl group, comprised of carbon and fluorine atoms. This unique composition renders the compound highly lipophobic, impeding its interactions with lipids and other biological molecules.


3-(Perfluorooctyl)-1,2-propenoxide (CAS 38565-53-6) References

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  2. Preparation of uniform-sized PELA microspheres with high encapsulation efficiency of antigen by premix membrane emulsification.  |  Wei, Q., et al. 2008. J Colloid Interface Sci. 323: 267-73. PMID: 18501376
  3. Engineering Quick- and Long-acting Naloxone Delivery Systems for Treating Opioid Overdose.  |  Sharifi, F., et al. 2021. Pharm Res. 38: 1221-1234. PMID: 34114163
  4. Perfluorinated phosphine and hybrid P-O ligands for Pd catalysed C-C bond forming reactions in solution and on Teflon supports.  |  Begum, F., et al. 2019. RSC Adv. 9: 28936-28945. PMID: 35528399
  5. Kinetic Stability of Toluene‐Perfluorooctane Emulsions  |  Bjarne Johansson, et al. 2007. Journal of Dispersion Science and Technology. Volume 28: Pages 121-132.
  6. Influence of Polymers on the Emulsified Hydrocarbon Liquid and on the Surfactant Stabilized Toluene/Perfluoro-octane Emulsions  |  Bjarne Johansson, et al. 2009. Journal of Dispersion Science and Technology. Volume 30,: Pages 989-996.
  7. Fluorinated epoxides as surface modifying agents of UV-curable systems  |   and M. Sangermano, R. Bongiovanni, G. Malucelli, A. Priola, A. Pollicino, A. Recca. 8 August 2003. Journal of Applied Polymer Science. Volume89, Issue6: Pages 1524-1529.
  8. Modification of an epoxy resin with a fluoroepoxy oligomer for improved mechanical and tribological properties  |  W Brostow, W Chonkaew, KP Menard… - Materials Science and …, 2009 - Elsevier. 15 May 2009,. Materials Science and Engineering: A. Volume 507, Issues 1–2,: Pages 241-251.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

3-(Perfluorooctyl)-1,2-propenoxide, 1 g

sc-260545
1 g
$99.00

3-(Perfluorooctyl)-1,2-propenoxide, 5 g

sc-260545A
5 g
$157.00

3-(Perfluorooctyl)-1,2-propenoxide, 25 g

sc-260545B
25 g
$451.00

3-(Perfluorooctyl)-1,2-propenoxide, 100 g

sc-260545C
100 g
$1342.00