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Merck

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:
98-01-1
Molecular Weight:
96.08
EC Number:
202-627-7
UNSPSC Code:
12352114
PubChem Substance ID:
329749151
Beilstein/REAXYS Number:
105755
MDL number:
MFCD00003229
Grade:
SAJ first grade
Assay:
≥99.0%
Application(s):
microbiology

Key Documents

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Product Name

Furfural, SAJ first grade, ≥99.0%

InChI key

HYBBIBNJHNGZAN-UHFFFAOYSA-N

InChI

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

SMILES string

O=Cc1ccco1

grade

SAJ first grade

assay

≥99.0%

form

liquid

availability

available only in Japan

dilution

(for analytical testing)

application(s)

microbiology

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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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Certificates of Analysis (COA)

Lot/Batch Number
A3231
A8962
A2646
A9443
A8353

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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
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
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
Vinit Choudhary et al.
Journal of the American Chemical Society, 135(10), 3997-4006 (2013-02-26)
5-(Hydroxymethyl)furfural (HMF) and levulinic acid production from glucose in a cascade of reactions using a Lewis acid (CrCl3) catalyst together with a Brønsted acid (HCl) catalyst in aqueous media is investigated. It is shown that CrCl3 is an active Lewis
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
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