Skip to Content
Merck
CN

408271

Tetrahydrofurfuryl acrylate

contains hydroquinone as inhibitor, monomethyl ether hydroquinone as inhibitor

Synonym(s):

THFA

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

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

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Tetrahydrofurfuryl acrylate, contains hydroquinone as inhibitor, monomethyl ether hydroquinone as inhibitor

InChI key

YNXCGLKMOXLBOD-UHFFFAOYSA-N

InChI

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

SMILES string

C=CC(=O)OCC1CCCO1

form

liquid

contains

hydroquinone as inhibitor
 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.)

Quality Level

100

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

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCW1425
MKCP1161
MKCL6032
MKCD8774
MKBX9086V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

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)
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
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)
View All Related Papers

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