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Sigma Aldrich 185914 Furfural 99% 100 mL
Marka
Stok Kodu
LB.SA.185914-100ML
Kısa Bilgi
Synonym(s): 2-Furaldehyde, Furan-2-carboxaldehyde Empirical Formula (Hill Notation): C5H4O2 CAS Number: 98-01-1 Molecular Weight: 96.08 Beilstein: 105755 EC Number: 202-627-7 MDL number: MFCD00003229 eCl@ss: 39150703 PubChem Substance ID: 57647750 NACRES: NA.21
| Sigma Aldrich 185914 Furfural 99% 100 mL |
| Synonym(s): 2-Furaldehyde, Furan-2-carboxaldehyde Empirical Formula (Hill Notation): C5H4O2 CAS Number: 98-01-1 Molecular Weight: 96.08 Beilstein: 105755 EC Number: 202-627-7 MDL number: MFCD00003229 eCl@ss: 39150703 PubChem Substance ID: 57647750 NACRES: NA.21 |
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PROPERTIES
vapor density 3.31 (vs air)
Quality Level 100 vapor pressure 13.5 mmHg ( 55 °C) Assay 99% form liquid autoignition temp. 599 °F expl. lim. 19.3 % refractive index n20/D 1.525 (lit.) bp 162 °C (lit.) mp −36 °C (lit.) density 1.16 g/mL at 25 °C (lit.) SMILES string [H]C(=O)c1ccco1 InChI 1S/C5H4O2/c6-4-5-2-1-3-7-5/h1-4H InChI key HYBBIBNJHNGZAN-UHFFFAOYSA-N DESCRIPTION
General description
Furfural is a heterocyclic aldehyde. It can be produced from agricultural raw materials containing pentosans[1] and lignocellulosic feedstock.[2] It is also obtained from xylose, via dehydration. Furan has various interesting properties, such as it thermosets easily, has physical strength and exhibits resistance to corrosion. It is a raw material for the production of various furan-based chemicals and solvents such as:[3] - methylfuran - furfuryl alcohol - tetrahydrofurfuryl alcohol - tetrahydrofuran - methyltetrahydrofuran - dihydropyran - furoic acid Application Furfural has been employed as a standard for the HPLC quantification of furfural in the autohydrolysate liquor obtained from microwave-irradiated maize bran.[4] It may be used in the preparation of γ-valerolactone (GVL)[5] and biofuel 2-methylfuran (51% yield).[6] Furfural undergoes hydrogenation in the vapor-phase over copper-containing catalysts to form furfuryl alcohol as the predominant product.[7] It may also be used to prepare gel precursors for phenol-furfural aerogels.[8] |
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