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Merck

185914

Sigma-Aldrich

Furfural

99%

Sinónimos:

2-Furaldehyde, Furan-2-carboxaldehyde

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About This Item

Fórmula empírica (notación de Hill):
C5H4O2
Número de CAS:
Peso molecular:
96.08
Beilstein/REAXYS Number:
105755
EC Number:
MDL number:
UNSPSC Code:
12352100
eCl@ss:
39150703
PubChem Substance ID:
NACRES:
NA.21

vapor density

3.31 (vs air)

Quality Level

vapor pressure

13.5 mmHg ( 55 °C)

assay

99%

form

liquid

autoignition temp.

599 °F

expl. lim.

19.3 %

refractive index

n20/D 1.525 (lit.)

bp

162 °C (lit.)

mp

−36 °C (lit.)

density

1.16 g/mL at 25 °C (lit.)

functional group

aldehyde

SMILES string

[H]C(=O)c1ccco1

InChI

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

InChI key

HYBBIBNJHNGZAN-UHFFFAOYSA-N

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General description

Furfural is a heterocyclic aldehyde. It can be produced from agricultural raw materials containing pentosans and lignocellulosic feedstock. It is also obtained from xylose, via dehydration. Furan has various interesting properties, such as it thermosets easily, has physical strength and exhibits resistance to corrosion. It is a raw material for the production of various furan-based chemicals and solvents such as:
  • methylfuran
  • furfuryl alcohol
  • tetrahydrofurfuryl alcohol
  • tetrahydrofuran
  • methyltetrahydrofuran
  • dihydropyran
  • furoic acid

Application

Furfural has been employed as a standard for the HPLC quantification of furfural in the autohydrolysate liquor obtained from microwave-irradiated maize bran. It may be used in the preparation of γ-valerolactone (GVL) and biofuel 2-methylfuran (51% yield).
Furfural undergoes hydrogenation in the vapor-phase over copper-containing catalysts to form furfuryl alcohol as the predominant product. It may also be used to prepare gel precursors for phenol-furfural aerogels.

signalword

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

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

136.4 °F - closed cup

flash_point_c

58 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Visite la Librería de documentos

Hydrogenation of furfural over copper-containing catalysts.
Seo G and Chon H.
J. Catal., 67(2), 424-429 (1981)
Inhibition effects of furfural on aerobic batch cultivation of Saccharomyces cerevisiae growing on ethanol and/or acetic acid.
Taherzadeh MJ, et al.
Journal of Bioscience and Bioengineering, 90(4), 374-380 (2000)
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)
Zeitsch KJ.
The chemistry and technology of furfural and its many by-products. , 13, 3-3 (2000)
Synthesis of organic and carbon aerogels from phenol-furfural by two-step polymerization.
Wu D and Fu R.
Microporous and Mesoporous Materials : The Official Journal of the International Zeolite Association, 96(1), 115-120 (2006)

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