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Merck

W248908

Sigma-Aldrich

Furfural

≥98%, FCC, FG

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
FEMA Number:
2489
Beilstein/REAXYS Number:
105755
EC Number:
Council of Europe no.:
2014
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
13.018
NACRES:
NA.21

biological source

synthetic

Quality Level

grade

FG
Fragrance grade
Halal
Kosher

agency

follows IFRA guidelines
meets purity specifications of JECFA

reg. compliance

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 117
FDA 21 CFR 175.105

vapor density

3.31 (vs air)

vapor pressure

13.5 mmHg ( 55 °C)

assay

≥98%

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.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

no known allergens

organoleptic

almond; baked; bread; woody; sweet

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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Application


  • Intermolecular Diels-Alder Cycloadditions of Furfural-Based Chemicals from Renewable Resources.: Focuses on the regio- and diastereoselectivity of furfural in reactions with alkenes, highlighting its potential in developing bio-based polymers (Galkin and Ananikov, 2021).

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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Lilong Zhou et al.
Bioresource technology, 129, 450-455 (2012-12-26)
A new kind of bifunctional ionic liquid catalysts was synthesized to degrade microcrystalline cellulose in [BMIM]Cl at atmospheric pressure. The effects of reaction temperature, amount of catalysts, reaction time, ionic liquid purity and cellulose concentration on conversion were investigated. At
Arvind H Jadhav et al.
Bioresource technology, 132, 342-350 (2013-02-26)
Acidity modified silver exchanged silicotungstic acid (AgSTA) catalyst was prepared and characterized by X-ray diffraction, FT-IR spectroscopy, Raman spectroscopy, FT-IR pyridine adsorption, SEM imaging, EDX mapping, and antimicrobial activity was also tested. The catalytic activity was evaluated for the dehydration
Jianghua He et al.
ChemSusChem, 6(1), 61-64 (2012-12-12)
It's nano: Small and uniform chromium nanoparticles, either preformed or generated in situ, effectively catalyze the conversion of glucose into 5-hydroxymethyl furfural. The results compare favorably with those achieved by using a catalyst system based on divalent CrCl(2) in ionic
Reetta Karinen et al.
ChemSusChem, 4(8), 1002-1016 (2011-07-06)
Furfurals are important intermediates in the chemical industry. They are typically produced by homogeneous catalysis in aqueous solutions. However, heterogeneously catalyzed processes would be beneficial in view of the principles of green chemistry: the elimination of homogeneous mineral acids makes
Tim Ståhlberg et al.
ChemSusChem, 4(4), 451-458 (2011-01-29)
The synthesis of 5-(hydroxymethyl)furfural (HMF) in ionic liquids is a field that has grown rapidly in recent years. Unique dissolving properties for crude biomass in combination with a high selectivity for HMF formation from hexose sugars make ionic liquids attractive

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