shoyu furanone

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

CAS: 27538-09-6 C7 H10 O3 MW: 142.15430000 caramellic caramellic

Identification

Nameshoyu furanone
IUPAC5-ethyl-4-hydroxy-2-methylfuran-3-one
CAS Number27538-09-6
EINECS248-513-0
FDA UNIIPG3201707P
Molecular FormulaC7 H10 O3
Molecular Weight142.15430000
MDL NumberMFCD03411593
Nikkaji NumberJ250.532K
CoE Number13084

Regulatory

JECFA Food Flavoring1449 2-ethyl-4-hydroxy-5-methyl-3(2H)-furanone
DG SANTE Food Flavourings13.084 2-ethyl-4-hydroxy-5-methyl-3-(2H)-furanone
FEMA Number3623
FDANo longer provide for the use of these seven synthetic flavoring substances

Physical Properties

Appearance yellow to brown viscous liquid or crystals (est)
Assay 96.00 to 100.00
Food Chemicals Codex Listed No
Specific Gravity 1.13300 to 1.14300 @ 25.00 °C.
Pounds per Gallon - (est). 9.428 to 9.511
Refractive Index 1.50900 to 1.51400 @ 20.00 °C.
Melting Point 31.00 to 35.00 °C. @ 760.00 mm Hg
Boiling Point 248.00 to 249.00 °C. @ 760.00 mm Hg
Vapor Pressure 0.012000 mmHg @ 25.00 °C. (est)
Flash Point > 212.00 °F. TCC ( > 100.00 °C. )
logP (o/w) 0.434 (est)
Soluble in alcohol
Stability alcohol, good

Cosmetic Information

CosIngcosmetic data
Cosmetic Usesperfuming agents

Organoleptic Properties

Odor Strength high ,
Substantivity 168 hour(s) at 10.00 % in dipropylene glycol
Odor Description
at 0.10 % in propylene glycol.
Sweet, caramellic, bready, maple, brown sugar with burnt undernotes
Taste Description at 20.00 ppm.

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryflavor and fragrance agents
RIFM Fragrance Material Safety AssessmentSearch
Recommendation for shoyu furanone usage levels up to1.0000 % in the fragrance concentrate.
Maximised Survey-derived Daily Intakes (MSDI-EU)160.00 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA)13.00 (μg/capita/day)
Structure ClassII
baked goods1.00000
beverages(nonalcoholic)1.00000
beverages(alcoholic)0.40000
breakfast cereal-
cheese-
chewing gum10.00000
condiments / relishes-
confectionery froastings0.25000
egg products-
fats / oils-
fish products-
frozen dairy-
fruit ices-
gelatins / puddings1.50000
granulated sugar-
gravies0.50000
hard candy1.00000
imitation dairy0.25000
instant coffee / tea-
jams / jellies-
meat products0.50000
milk products0.25000
nut products-
other grains-
poultry-
processed fruits-
processed vegetables-
reconstituted vegetables-
seasonings / flavors-
snack foods-
soft candy-
soups-
sugar substitutes-
sweet sauces-

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O'Laughlin Industries Inc.

Manufacturer of chemicals and ingredients used in flavors, fragrances, food, beverages and cosmetics

Leading the Flavor and Fragrance Industry since 1980.

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OQEMA

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The John D. Walsh Company, Inc

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Potential Uses

FR butterscotch FL caramel FL chocolate cocoa FR coffee FR floral FR fruit fruit jam FL fruit tropical fruit FR maple FL molasses FR oriental FR strawberry FL sugar brown sugar FR vanilla

Natural Occurrence

cheese PMC coffee PMC pineapple fruit shoyu PMC strawberry wild strawberry fruit

Synonyms

ethyl fraison ethyl furanone synthetic ethyl strawberry furanone ethyl-2 5-methyl 4-hydroxy 3 2H-furanone 5- ethyl-4-hydroxy-2-methyl furan-3(2H)-one 5- ethyl-4-hydroxy-2-methyl-3 2H furanone 5- ethyl-4-hydroxy-2-methyl-3(2H)-furanone 5- ethyl-4-hydroxy-2-methylfuran-3-one 5- ethyl-4-hydroxy-2-methylfuran-3(2H)-one 2- ethyl-4-hydroxy-5-methyl-3-(2H)-furanone 2- ethyl-4-hydroxy-5-methyl-3-(2H)-furanone in 20% P.G. 2- ethyl-4-hydroxy-5-methyl-3-(2H)-furanone natural 2- ethyl-4-hydroxy-5-methyl-3-(2H)-furanone natural 20% in P.G. 2- ethyl-4-hydroxy-5-methyl-3(2H)-furanone 3(2H)- furanone, 5-ethyl-4-hydroxy-2-methyl- homo furonol 20% in PG 4- hydroxy-5-ethyl-2-methyl-3(2H)-furanone maltarome (PFW) maltarome mixture (PFW) shoyu furanone soy furaneol soy furaneol synthetic soy furanone strawberry furanone, ethyl PubMed: Structural basis for the enzymatic formation of the key strawberry flavor compound 4-hydroxy-2,5-dimethyl-3(2H)-furanone. PubMed: Main odorants in Jura flor-sherry wines. Relative contributions of sotolon, abhexon, and theaspirane-derived compounds. PubMed: Identification of sulfur volatiles in canned orange juices lacking orange flavor. PubMed: Aroma extract dilution analysis of Cv. Marion (Rubus spp. hyb) and Cv. Evergreen (R. laciniatus L.) blackberries. PubMed: Enzymatic synthesis of stable, odorless, and powdered furanone glucosides by sucrose phosphorylase.