Skip to Content
Merck
All Photos(1)

Documents

408271

Sigma-Aldrich

Tetrahydrofurfuryl acrylate

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

Synonym(s):

THFA

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C8H12O3
CAS Number:
Molecular Weight:
156.18
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

form

liquid

Quality Level

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

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

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

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)
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
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)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service