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F19558

Sigma-Aldrich

Furan

98%

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About This Item

Empirical Formula (Hill Notation):
C4H4O
CAS Number:
Molecular Weight:
68.07
Beilstein:
103221
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

vapor density

2.35 (vs air)

vapor pressure

1672 mmHg ( 55 °C)
31.66 psi ( 55 °C)
493 mmHg ( 20 °C)
9.22 psi ( 20 °C)

Assay

98%

contains

0.025 wt. % BHT as inhibitor

expl. lim.

14.3 %

refractive index

n20/D 1.421 (lit.)

bp

32 °C/758 mmHg (lit.)

density

0.936 g/mL at 25 °C (lit.)

SMILES string

c1ccoc1

InChI

1S/C4H4O/c1-2-4-5-3-1/h1-4H

InChI key

YLQBMQCUIZJEEH-UHFFFAOYSA-N

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Pricing

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 1B - Flam. Liq. 1 - Muta. 2 - Skin Irrit. 2 - STOT RE 2

Supplementary Hazards

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

-32.8 °F - closed cup

Flash Point(C)

-36 °C - closed cup


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Customers Also Viewed

Carolin Neuwirth et al.
Molecular nutrition & food research, 56(9), 1363-1374 (2012-08-07)
Furan is a potent hepatotoxicant and liver carcinogen in rodents. However, short-term tests for genotoxicity of furan are inconclusive. The aim of this study was to assess the potential of furan to covalently bind to DNA, and to assess furan
C W Heppner et al.
Food additives and contaminants, 24 Suppl 1, 114-121 (2007-09-22)
Furan is an organic, volatile compound used in various chemical-manufacturing industries. Headspace gas chromatography is the analytical method of choice for obtaining reliable results on its occurrence. The presence of furan in some food items has been known since the
Rialet Pieters et al.
Environment international, 66, 71-78 (2014-02-18)
In South Africa, 26-50% of households use solid fuel for cooking food and heating houses. When used as fuel, wood and chlorinated waste are known sources of polychlorinated dibenzo-para-dioxins, polychlorinated dibenzofurans (PCDD/Fs), and polychlorinated biphenyls (PCBs). Here, we compare PCDD/F
Anna Francina Jackson et al.
Toxicology and applied pharmacology, 274(1), 63-77 (2013-11-05)
Furan is a chemical hepatocarcinogen in mice and rats. Its previously postulated cancer mode of action (MOA) is chronic cytotoxicity followed by sustained regenerative proliferation; however, its molecular basis is unknown. To this end, we conducted toxicogenomic analysis of B3C6F1
Joseph Salamoun et al.
Organic letters, 16(7), 2034-2037 (2014-03-20)
Two complementary approaches for the preparation of linked 5-membered heterocycles were developed. The Pd-catalyzed Suzuki-Miyaura cross-coupling with halogenated furan, thiophene, and selenophene led to higher overall yields, but C,H-bond activation was a more efficient strategy for the coupling at C(2)

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