11-1080
Furfural
SAJ first grade, ≥99.0%
Synonym(s):
2-Furaldehyde, 2-Furancarboxaldehyde
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About This Item
Empirical Formula (Hill Notation):
C5H4O2
CAS Number:
Molecular Weight:
96.08
EC Number:
202-627-7
UNSPSC Code:
12352114
PubChem Substance ID:
Beilstein/REAXYS Number:
105755
MDL number:
Assay:
≥99.0%
Grade:
SAJ first grade
grade
SAJ first grade
assay
≥99.0%
form
liquid
availability
available only in Japan
dilution
(for analytical testing)
application(s)
microbiology
SMILES string
O=Cc1ccco1
InChI
1S/C5H4O2/c6-4-5-2-1-3-7-5/h1-4H
InChI key
HYBBIBNJHNGZAN-UHFFFAOYSA-N
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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
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
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