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408271

Sigma-Aldrich

Tetrahydrofurfuryl acrylate

contains 500 ppm hydroquinone as inhibitor, 500 ppm monomethyl ether hydroquinone as inhibitor

Synonym(s):

THFA

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About This Item

Empirical Formula (Hill Notation):
C8H12O3
CAS Number:
2399-48-6
Molecular Weight:
156.18
EC Number:
219-268-7
MDL number:
MFCD00014516
UNSPSC Code:
12162002
PubChem Substance ID:
24865555
NACRES:
NA.23

form

liquid

Quality Level

100

contains

500 ppm hydroquinone as inhibitor
500 ppm monomethyl ether hydroquinone as inhibitor

refractive index

n20/D 1.46 (lit.)

bp

87 °C/9 mmHg (lit.)

density

1.064 g/mL at 25 °C (lit.)

SMILES string

C=CC(=O)OCC1CCCO1

InChI

1S/C8H12O3/c1-2-8(9)11-6-7-4-3-5-10-7/h2,7H,1,3-6H2

InChI key

YNXCGLKMOXLBOD-UHFFFAOYSA-N

Related Categories

Application

Tetrahydrofurfuryl acrylate may be used as an acrylic matrix for silver nanoparticles/polymer nanocomposites . It can form copolymers with butadiene. Prior to transfer printing, cellulosic and proteinic fibers are grafted with THFA.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Lauryl acrylate technical grade, 90%

Sigma-Aldrich

447315

Lauryl acrylate

4-Hydroxybutyl acrylate 90%, contains 50 ppm monomethyl ether hydroquinone as inhibitor, 300 ppm hydroquinone as inhibitor

Sigma-Aldrich

275573

4-Hydroxybutyl acrylate

Fan Xie et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 22(5), 455-460 (2021-01-17)
A chiral adduct formed between a chiral carboxylic acid, tetrahydro-2-furoic acid (THFA), and a chiral ester, propylene oxide (PO), was investigated using rotational spectroscopy and DFT calculations. Isolated THFA exists dominantly as three different conformers: I, II, and III in
David A Korasick et al.
Biophysical journal, 114(12), 2833-2843 (2018-06-21)
Homooligomerization of proline utilization A (PutA) bifunctional flavoenzymes is intimately tied to catalytic function and substrate channeling. PutA from Bradyrhizobium japonicum (BjPutA) is unique among PutAs in that it forms a tetramer in solution. Curiously, a dimeric BjPutA hot spot
Transfer printing of cellulosic and proteinic fabrics.
El-Molla MM, et al.
Advances in Polymer Technology, 20(4), 296-304 (2001)
Some new butadiene copolymers.
Marvel CS, et al.
Journal of Polymer Science, 8(6), 599-605 (1952)
Katja U Schneider et al.
BMC cancer, 11, 102-102 (2011-03-24)
DNA methylation in the SHOX2 locus was previously used to reliably detect lung cancer in a group of critical controls, including 'cytologically negative' samples with no visible tumor cell content, at a high specificity based on the analysis of bronchial
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