≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 15 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Furaneol is a flavor compound that occurs in fruits such as pineapple, strawberry and mango.
4-Hydroxy-2,5-dimethyl-3(2H)-furanone (HDMF, DMHF) is a caramel-like odor compound identified by GC-MS and GCMS/MS in a pentose-based Maillard reaction system. The solubility data of DMHF in six different solvents at an atmospheric pressure of 0.10 MPa in the temperature range of 283.15 K to 313.15 K were studied by a dynamic method. The enantiomers of DMHF were reported to be separated by capillary electrophoresis. Commercially it is synthesized from L-rhamnose. DMHF has been identified as an acidic flavor enhancer in premium fish sauce samples from Thailand by aroma extract dilution analysis (AEDA). It was identified as a key aroma compound in wheat distillers grains (DG). It is reported to be the main flavor compound in strawberries, and its biosynthesis has been reported. HDMF is found in various fruits such as pineapple, strawberries, and grapes, and is also found in beef broth, fried coffee, bread crust, roast beef, roast sesame, and beef stew.
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Klasse | Dihydrofurans |
| Subclass | Furanones |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Furanones |
| Alternative Parents | Vinylogous esters Cyclic ketones Oxacyclic compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | 3-furanone - Vinylogous ester - Cyclic ketone - Ketone - Oxacycle - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic heteromonocyclic compound |
| Beschreibung | This compound belongs to the class of organic compounds known as furanones. These are compounds containing a furan ring bearing a ketone group. |
| External Descriptors | cyclic ketone - furans - enol |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Datum | Artikel |
|---|---|---|---|
 F2520638 | Certificate of Analysis | Jun 14, 2025 | F118422 |
| F2520644 | Certificate of Analysis | Jun 14, 2025 | F118422 |
| F2520645 | Certificate of Analysis | Jun 14, 2025 | F118422 |
| F2520646 | Certificate of Analysis | Jun 14, 2025 | F118422 |
| A2218399 | Certificate of Analysis | Jan 03, 2022 | F118422 |
| A2218400 | Certificate of Analysis | Jan 03, 2022 | F118422 |
| A2218401 | Certificate of Analysis | Jan 03, 2022 | F118422 |
| D2415385 | Certificate of Analysis | Jan 03, 2022 | F118422 |
| J2325063 | Certificate of Analysis | Jan 03, 2022 | F118422 |
| L2419065 | Certificate of Analysis | Jan 03, 2022 | F118422 |
| Löslichkeit | Slightly soluble in water, soluble in methanol |
|---|---|
| Empfindlichkeit | Air & Heat Sensitive |
| Brechungsindex | 1.435 |
| Siedepunkt (°C) | 230℃ |
| Schmelzpunkt (°C) | 75-80°C |
| Molekulargewicht | 128.130 g/mol |
| XLogP3 | 0.700 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 128.047 Da |
| Monoisotopic Mass | 128.047 Da |
| Topological Polar Surface Area | 46.500 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 181.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
