3-Hydroxy-4-methyl-5-ethyl-2(5H)furanone

3-Hydroxy-4-methyl-5-ethyl-2(5H)furanone Basic information
Product Name:3-Hydroxy-4-methyl-5-ethyl-2(5H)furanone
Synonyms:5-ETHYL-4-METHYL-3-HYDROXYFURANONE;5-ETHYL-3-HYDROXY-4-METHYL-2(5H)-FURANONE;5-ETHYL-3-HYDROXY-4-METHYL-5H-FURAN-2-ONE;2(5H)-Furanone, 5-ethyl-3-hydroxy-4-methyl-;2-Hexenoic acid, 2,4-dihydroxy-3-methyl-, gamma-lactone;4-Methyl-5-ethyl-3-hydroxyfuranone;5-ethyl-3-hydroxy-4-methyl-2(5h)-furanon;MAPLE FURANONE
CAS:698-10-2
MF:C7H10O3
MW:142.15
EINECS:211-811-6
Product Categories:food additive;Alphabetical Listings;E-F;Flavors and Fragrances
Mol File:698-10-2.mol
3-Hydroxy-4-methyl-5-ethyl-2(5H)furanone Structure
3-Hydroxy-4-methyl-5-ethyl-2(5H)furanone Chemical Properties
Melting point 31-35 °C(lit.)
Boiling point 83-86 °C0.5 mm Hg(lit.)
density 1.1643 (rough estimate)
FEMA 3153 | 5-ETHYL-3-HYDROXY-4-METHYL-2(5H)-FURANONE
refractive index n20/D 1.49(lit.)
Fp >230 °F
storage temp. 2-8°C
solubility Chloroform (Slightly), Methanol (Slightly)
form powder to lump to clear liquid
pka9.28±0.40(Predicted)
color White or Colorless to Yellow
Odorat 0.01 % in dipropylene glycol. sweet fruity caramellic maple fenugreek brown sugar nutty chicory praline butterscotch
Odor Typecaramellic
FreezingPoint 25.0 to 29.0 ℃
JECFA Number222
Stability:Hygroscopic
InChIKeyIUFQZPBIRYFPFD-UHFFFAOYSA-N
LogP0.09
CAS DataBase Reference698-10-2(CAS DataBase Reference)
NIST Chemistry Reference2(5H)-furanone, 5-ethyl-3-hydroxy-4-methyl-(698-10-2)
EPA Substance Registry System2(5H)-Furanone, 5-ethyl-3-hydroxy-4-methyl- (698-10-2)
Safety Information
Safety Statements 24/25
RIDADR UN 3335
WGK Germany 3
HS Code 29322090
MSDS Information
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3-Hydroxy-4-methyl-5-ethyl-2(5H)furanone English
ACROS English
SigmaAldrich English
3-Hydroxy-4-methyl-5-ethyl-2(5H)furanone Usage And Synthesis
Chemical Propertieslight yellow liqui
Chemical PropertiesAbhexone has been found in, for example, lovage and roasted coffee. It has a bouillon-like, coffee and lovage aroma, depending on its concentration. It can be prepared starting from alkyl 2-oxobutanoate either by self-condensation followed subsequently by decarbomethoxylation or by condensation with propionaldehyde and subsequent cyclization . Alkyl 2-oxobutanoate is available from acrylaldehyde and sodium cyanide via alkyl 2-hydroxy-3-butenoate or by reaction of dialkyloxalate with ethyl magnesium bromide . It is used for aromatization of food.
Chemical Properties5-Ethyl-3-hydroxy-4-methyl-2(5H)-furanone has a sweet, maple, caramel odor.
OccurrenceReported found in coffee.
Uses5-Ethyl-3-hydroxy-4-methyl-2(5H)-furanone is an odorant found in grape stems, Jura Flor-Sherry wines and roasted arabica coffee.
DefinitionChEBI: 5-ethyl-3-hydroxy-4-methyl-2(5H)-furanone is a butenolide. It has a role as a metabolite.
Taste threshold valuesTaste characteristics at 50 ppm: sweet, fruity with brown maple note.
3-Hydroxy-4-methyl-5-ethyl-2(5H)furanone Preparation Products And Raw materials
DL-1-Phenethylalcohol 5-Hydroxymethylfurfural Leaf alcohol 4-Hydroxy-2-methyl-5-ethyl-3(2H)furanone 2(5H)-Furanone 3-Hydroxy-4-methyl-5-ethyl-2(5H)furanone 2-(4-Hydroxybenzyl)-3-(4-hydroxyphenyl)-4-hydroxy-5-oxo-2,5-dihydrofuran-2-carboxylic acid methyl ester 3-(3-BROMOBENZOYL)-4-HYDROXY-5H-SPIRO[FURAN-2,2'-INDENE]-1',3',5-TRIONE 3-HYDROXY-3METHYL-5ETHYL-2(5H)-FURANONE 4,5-Dimethyl-3-hydroxy-2,5-dihydrofuran-2-one Triacetin 4-METHYL-2(5H)-FURANONE AKOS B024631 AKOS B024633 BUTYROLACTONE I

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