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Sigma-Aldrich

Tetrahydrofurfuryl acrylate

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

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Synonym(s):
THFA
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

Signal Word

Warning

Hazard Statements

H315,H319,H412

Hazard Classifications

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

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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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
A new and convenient route to polyacrylate/silver nanocomposites by light-induced cross-linking polymerization
Balan L, et al.
Progress in Organic Coatings, 62(3), 351-357 (2008)
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
Some new butadiene copolymers.
Marvel CS, et al.
Journal of Polymer Science, 8(6), 599-605 (1952)
Transfer printing of cellulosic and proteinic fabrics.
El-Molla MM, et al.
Advances in Polymer Technology, 20(4), 296-304 (2001)
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