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753092

Sigma-Aldrich

Pentafluorophenyl acrylate

contains <200 ppm monomethyl ether hydroquinone as inhibitor, 98%

Synonym(s):

2-Propenoic acid pentafluorophenyl ester

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About This Item

Empirical Formula (Hill Notation):
C9H3F5O2
CAS Number:
71195-85-2
Molecular Weight:
238.11
MDL number:
MFCD00042330
UNSPSC Code:
12162002
PubChem Substance ID:
329766334
NACRES:
NA.23

Assay

98%

form

liquid

contains

<200 ppm monomethyl ether hydroquinone as inhibitor

refractive index

n/D 1.434

density

1.446

storage temp.

2-8°C

SMILES string

Fc1c(F)c(F)c(OC(=O)C=C)c(F)c1F

InChI

1S/C9H3F5O2/c1-2-3(15)16-9-7(13)5(11)4(10)6(12)8(9)14/h2H,1H2

InChI key

RFOWDPMCXHVGET-UHFFFAOYSA-N

Related Categories

Application

Acrylate monomer with an activated ester for coupling (esterification/amidation) reactions
Pentafluorophenyl acrylate may be used in the preparation of highly porous polymers (poly HIPs). Pentafluorophenyl acrylate (PFPA) can undergo reversible addition fragmentation transfer (RAFT) polymerization with oligoethylene glycol acrylate (OEGA) or diethylene glycol acrylate (DEGA).

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

154.4 °F - closed cup

Flash Point(C)

68 °C - closed cup

Certificates of Analysis (COA)

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Reactive thiol-ene emulsion-templated porous polymers incorporating pentafluorophenyl acrylate
Kircher L, et al.
Polymer, 54(7), 1755-1761 (2013)
Factors influencing the synthesis and the post-modification of PEGylated pentafluorophenyl acrylate containing copolymers
Beija M, et al.
European Polymer Journal, 49, 3060?3071-3060?3071 (2013)
Yuwaporn Pinyakit et al.
Journal of materials chemistry. B, 8(3), 454-464 (2019-12-14)
Recently, pH-responsive polymeric micelles have gained significant attention as effective carriers for anti-cancer drug delivery. Herein, pH-responsive polymeric micelles were constructed by a simple post-polymerization modification of a single homopolymer, poly(pentafluorophenyl acrylate) (PPFPA). The PPFPA was first subjected to modification

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