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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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$263.00
5 G
$893.00

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1 G
$263.00
5 G
$893.00

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

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Quality Level

100

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).[1] Pentafluorophenyl acrylate (PFPA) can undergo reversible addition fragmentation transfer (RAFT) polymerization with oligoethylene glycol acrylate (OEGA) or diethylene glycol acrylate (DEGA). [2]

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

154.4 °F - closed cup

flash_point_c

68 °C - closed cup

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Certificates of Analysis (COA)

Lot/Batch Number
MKCT8603
MKCJ4365
MKBZ2421V
MKBT3877V
MKBT5920V

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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)
Reactive thiol-ene emulsion-templated porous polymers incorporating pentafluorophenyl acrylate
Kircher L, et al.
Polymer, 54(7), 1755-1761 (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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