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Merck

04623

Supelco

2-Furaldehyd

analytical standard

Synonym(e):

Furan-2-carboxaldehyd, Furfural

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About This Item

Empirische Formel (Hill-System):
C5H4O2
CAS-Nummer:
Molekulargewicht:
96.08
Beilstein:
105755
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
85151701
PubChem Substanz-ID:
NACRES:
NA.24

Qualitätsniveau

Qualität

analytical standard

Dampfdichte

3.31 (vs air)

Dampfdruck

13.5 mmHg ( 55 °C)

Assay

≥98.5% (GC)

Selbstzündungstemp.

599 °F

Haltbarkeit

limited shelf life, expiry date on the label

Expl.-Gr.

19.3 %

Verunreinigungen

≤0.5% water

Brechungsindex

n20/D 1.522-1.528
n20/D 1.525 (lit.)

bp

162 °C (lit.)

mp (Schmelzpunkt)

−36 °C (lit.)

Dichte

1.16 g/mL at 25 °C (lit.)

Anwendung(en)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Format

neat

SMILES String

[H]C(=O)c1ccco1

InChI

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

InChIKey

HYBBIBNJHNGZAN-UHFFFAOYSA-N

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Allgemeine Beschreibung

Furfural is a furan derivative obtained from renewable biomass-derived carbohydrates.

Anwendung

Furfural is a sustainable alternative for petroleum-based building blocks used in the production of fine chemicals, plastics, etc and also offers a promising, rich platform for lignocellulosic biofuels.

Signalwort

Danger

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 2

Flammpunkt (°F)

136.4 °F - closed cup

Flammpunkt (°C)

58 °C - closed cup


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Die Dokumentenbibliothek aufrufen

Sofia Tallarico et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 250, 119367-119367 (2021-01-06)
Chemocatalytic conversion of cellulose into lactic acid is a valuable alternative to simple sugar fermentation. Nevertheless, the procedures still need optimization to be translated to the industrial scale. Such translation would benefit by on-line monitoring of reaction parameters by fast
Production of 5-hydroxymethylfurfural and furfural by dehydration of biomass-derived mono-and poly-saccharides.
Chheda JN, et al.
Green Chemistry, 9(4), 342-350 (2007)
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
T B Adams et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 35(8), 739-751 (1997-08-01)
The Expert Panel of the Flavor and Extract Manufacturers' Association (FEMA) has assessed the safety of furfural for its continued use as a flavour ingredient. The safety assessment takes into account the current scientific information on exposure, metabolism, pharmacokinetics, toxicology
Jean-Paul Lange et al.
ChemSusChem, 5(1), 150-166 (2012-01-04)
Furfural offers a promising, rich platform for lignocellulosic biofuels. These include methylfuran and methyltetrahydrofuran, valerate esters, ethylfurfuryl and ethyltetrahydrofurfuryl ethers as well as various C(10)-C(15) coupling products. The various production routes are critically reviewed, and the needs for improvements are

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