Methoxymethylfurfural
| Names | |
|---|---|
| Preferred IUPAC name 5-[(Methoxy)methyl]furan-2-carbaldehyde | |
| Other names 5-Methoxymethyl furfural; Methoxymethylfurfurol; 5-(Methoxymethyl)furan-2-carbaldehyde; 5-Methoxymethylfurfural; 5-(Methoxymethyl)-2-furaldehyde | |
| Identifiers | |
| 3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.149.478 | 
| PubChem CID | |
| UNII | |
| CompTox Dashboard (EPA) | |
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| Properties | |
| C7H8O3 | |
| Molar mass | 140.138 g·mol−1 | 
| Appearance | Colorless liquid | 
| Density | 1140 kg/m3 | 
| Melting point | −8 °C (18 °F; 265 K) | 
| Boiling point | 109 to 111 °C (228 to 232 °F; 382 to 384 K) at 11-12 tor | 
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
| Main hazards | Skin irritation/Skin sensitizer | 
| Related compounds | |
| Related furan-2-carbaldehydes | Furfural Hydroxymethylfurfural | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Methoxymethylfurfural (MMF or 5-methoxymethylfuran-2-carbaldehyde) is an organic compound derived from dehydration of sugars and subsequent etherification with methanol. This colorless liquid is soluble in a wide range of solvents including lower alcohols. The molecule is a derivative of furan, containing both aldehyde and ether (methoxymethyl) functional groups. MMF has been detected in the leaves and roots of Chilean Jaborosa magellanica (Solanaceae). It has a typical odor suggestive of maraschino cherries. MMF can be made from a wide range of carbohydrate containing feedstocks including sugar, starch and cellulose using a chemical catalytic process and is a potential "carbon-neutral" feedstock for fuels and chemicals.