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V900723

Sigma-Aldrich

5-Methylfurfural

Vetec™, reagent grade, 98%

Sinonimo/i:

5-Methyl-2-furaldehyde

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About This Item

Formula empirica (notazione di Hill):
C6H6O2
Numero CAS:
620-02-0
Peso molecolare:
110.11
Beilstein:
106895
Numero CE:
210-622-6
Numero MDL:
MFCD00003232
Codice UNSPSC:
12352100
ID PubChem:
329830095

Grado

reagent grade

Nome Commerciale

Vetec™

Saggio

98%

Indice di rifrazione

n20/D 1.531 (lit.)

P. eboll.

187 °C (lit.)

Densità

1.107 g/mL at 25 °C (lit.)

Stringa SMILE

[H]C(=O)c1ccc(C)o1

InChI

1S/C6H6O2/c1-5-2-3-6(4-7)8-5/h2-4H,1H3
OUDFNZMQXZILJD-UHFFFAOYSA-N

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Note legali

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

161.6 °F - closed cup

Punto d’infiammabilità (°C)

72 °C - closed cup

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[Gas-chromatographic determination of furfural, methylfurfural and furyl alcohol in air].
V V Tarasov
Gigiena truda i professional'nye zabolevaniia, (12)(12), 53-54 (1985-12-01)
Nick Wierckx et al.
Microbial biotechnology, 3(3), 336-343 (2011-01-25)
The formation of toxic fermentation inhibitors such as furfural and 5-hydroxy-2-methylfurfural (HMF) during acid (pre-)treatment of lignocellulose, calls for the efficient removal of these compounds. Lignocellulosic hydrolysates can be efficiently detoxified biologically with microorganisms that specifically metabolize the fermentation inhibitors
Shahabuddin et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 29(10), 719-721 (1991-10-01)
The furans, furfural and methylfurfural, are dietary mutagens that are present in various food products and beverages. AT base-pair-depleted calf thymus DNA was prepared by the action of pea seed single-strand-specific nuclease on native DNA. Compared with furan-treated native DNA
M T Jafari et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 25(6), 801-805 (2009-06-18)
A novel technique, corona discharge ion mobility spectrometry (CD-IMS), was developed for the qualitative and quantitative determination of 2-furfural (F) and 5-methyl-2-furfural (MF) in aqueous solutions. The limits of detection (LODs) were 5.3 x 10(-3) microg/mL for F and 6.7
M Pitié et al.
Nucleic acids research, 28(24), 4856-4864 (2000-01-11)
Mechanisms of DNA oxidation by copper complexes of 3-Clip-Phen and its conjugate with a distamycin analogue, in the presence of a reductant and air, were studied. Characterisation of the production of 5-methylenefuranone (5-MF) and furfural, associated with the release of
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