Skip to Content
Merck
All Photos(2)

Documents

319910

Sigma-Aldrich

Furfural

ACS reagent, 99%

Synonym(s):

2-Furaldehyde, Furan-2-carboxaldehyde

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C5H4O2
CAS Number:
Molecular Weight:
96.08
Beilstein:
105755
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21

grade

ACS reagent

Quality Level

vapor density

3.31 (vs air)

vapor pressure

13.5 mmHg ( 55 °C)

Assay

99%

form

liquid

autoignition temp.

599 °F

expl. lim.

19.3 %

impurities

≤0.02 meq/g

evapn. residue

≤0.5%

refractive index

n20/D 1.525 (lit.)

bp

162 °C (lit.)

mp

−36 °C (lit.)

density

1.16 g/mL at 25 °C (lit.)

SMILES string

[H]C(=O)c1ccco1

InChI

1S/C5H4O2/c6-4-5-2-1-3-7-5/h1-4H

InChI key

HYBBIBNJHNGZAN-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Furfural can be used as a reactant to synthesize:
  • Furfuryl alcohol via Cannizzaro reaction.
  • Furancarboxylic acid via nickel-catalyzed oxidation.
  • Dimer via base-catalyzed aldol condensation with cyclopentanone.

Signal Word

Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Chronic 3 - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

136.4 °F - closed cup

Flash Point(C)

58 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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.

Already Own This Product?

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

Visit the Document Library

Domino reaction catalyzed by zeolites with Brønsted and Lewis acid sites for the production of γ-valerolactone from furfural.
Linh Bui et al.
Angewandte Chemie (International ed. in English), 52(31), 8022-8025 (2013-06-13)
Integrated furfural production as a renewable fuel and chemical platform from lignocellulosic biomass.
Cai CM, et al.
Journal of Chemical Technology and Biotechnology, 89(1), 2-10 (2014)
Production of feruloylated arabinoxylo-oligosaccharides from maize (Zea mays) bran by microwave-assisted autohydrolysis.
Rose DJ and Inglett GE.
Food Chemistry, 119(4), 1613-1618 (2010)
Selective hydrogenation of furfural and levulinic acid to biofuels on the ecofriendly Cu-Fe catalyst.
Yan K and Chen A.
Fuel: The Science and Technology of Fuel and Energy, 115, 101-108 (2014)
Jianmin Zhang et al.
Journal of medicinal chemistry, 50(8), 1850-1864 (2007-03-27)
The 3C-like protease (3CLpro), which controls the severe acute respiratory syndrome (SARS) coronavirus replication, has been identified as a potential target for drug design in the treatment of SARS. A series of tetrapeptide phthalhydrazide ketones, pyridinyl esters, and their analogs

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