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General Material Information

Preferred name 2-methyl furan
Trivial Name 2-Methylfuran
Short Description 2-methylfuran
Formula C5 H6 O
CAS Number 534-22-5
FEMA Number 4179
Flavis Number 13.03
ECHA Number 208-594-5
FDA UNII 51O3BGW3F2
Nikkaji Number J6.337A
Beilstein Number 0103733
MDL MFCD00003248
COE Number 2209
Bio Activity Summary External link
NMR Predictor External link
JECFA Food Flavoring 1487 2-methylfuran
FDA Patent No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm 534-22-5 ; 2-METHYLFURAN
Synonyms
  • furan, 2-methyl-
  • alpha- methyl furan
  • 2-methyl furan natural
  • 2-methylfuran
  • silvan
  • sylvan
  • 2-Methylfuran
  • α-Methylfuran
  • 5-Methylfuran
  • NSC 3707
  • NSC 5211

US / EU / FDA / JECFA / FEMA / Scholar / Patents

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Literature & References

2-methylfuran
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:534-22-5
Pubchem (cid):10797
Pubchem (sid):134977217
Pherobase:View
Publications by Info
substances containing furan substitution
Publications by US Patents
3,981,920 - Method for preparing cyclopentenone derivatives
Publications by PubMed
Selectivity Control in the Tandem Aromatization of Bio-Based Furanics Catalyzed by Solid Acids and Palladium.
Environmental Variables Associated with Hantavirus Reservoirs and Other Small Rodent Species in Two National Parks in the Paraná Delta, Argentina: Implications for Disease Prevention.
Odisolane, a Novel Oxolane Derivative, and Antiangiogenic Constituents from the Fruits of Mulberry (Morus alba L.).
Relative importance and interactions of furan precursors in sterilised, vegetable-based food systems.
An efficient method for the simultaneous determination of furan, 2-methylfuran and 2-pentylfuran in fruit juices by headspace solid phase microextraction and gas chromatography-flame ionisation detector.
Spatially resolved sampling reveals dynamic microbial communities in rising hydrothermal plumes across a back-arc basin.
Furanic compounds and furfural in different coffee products by headspace liquid-phase micro-extraction followed by gas chromatography-mass spectrometry: survey and effect of brewing procedures.
Mushrooms and Health Summit proceedings.
Characterization of the major odor-active compounds in Thai durian ( Durio zibethinus L. 'Monthong') by aroma extract dilution analysis and headspace gas chromatography-olfactometry.
Impact of crema on the aroma release and the in-mouth sensory perception of espresso coffee.
Amino acid catalysis of 2-alkylfuran formation from lipid oxidation-derived α,β-unsaturated aldehydes.
Metabolomic approach for determination of key volatile compounds related to beef flavor in glutathione-Maillard reaction products.
Quantitative analysis of volatiles from solid matrices of vegetable origin by high concentration capacity headspace techniques: determination of furan in roasted coffee.
Development of an analytical method and survey of foods for furan, 2-methylfuran and 3-methylfuran with estimated exposure.
Chemical and biochemical study of industrially produced San Simón da Costa smoked semi-hard cow's milk cheeses: Effects of storage under vacuum and different modified atmospheres.
Formation of furan and methylfuran by maillard-type reactions in model systems and food.
Detection of fungal development in closed spaces through the determination of specific chemical targets.
Formation of furan and methylfuran from ascorbic acid in model systems and food.
Quality and flavour stability of coffee substitute prepared by extrusion of wheat germ and chicory roots.
Aroma extraction dilution analysis of Sauternes wines. Key role of polyfunctional thiols.
[Listeriosis must be identified and notified--also the mild cases. Probably a more common disease than the statistics show, ready-to-eat foods are risk sources].
Possible interaction between warfarin and cranberry juice.
Volatile composition of coffee berries at different stages of ripeness and their possible attraction to the coffee berry borer Hypothenemus hampei (Coleoptera: Curculionidae).
Antioxidative activities of heterocyclic compounds formed in brewed coffee.
Differentiation of the aromas of Merlot and Cabernet Sauvignon wines using sensory and instrumental analysis.
Effect of crop development on biogenic emissions from plant populations grown in closed plant growth chambers.
Clastogenicity of furans found in food.

Other Information

(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
FDA Substances Added to Food (formerly EAFUS):View
CHEMBL:View
HMDB (The Human Metabolome Database):HMDB13749
FooDB:FDB012718
Export Tariff Code:2932.19.5100
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View
EFSA Update of results on the monitoring of furan levels in food:Read Report
EFSA Previous report: Results on the monitoring of furan levels in food:Read Report
EFSA Report of the CONTAM Panel on provisional findings on furan in food:Read Report

PhysChem Properties

Material listed in food chemical codex No
Molecular weight 82.102020263672
Specific gravity @ 25 °C
Pounds per Gallon 7.555 to 7.63
Refractive Index 1.431 to 1.437 @ 20 °C
Boiling Point 63 to 66°C @ 760 mm Hg
Vapor Pressure 176.098007 mmHg @ 25 °C
Vapor Density 2.8
Flash Point TCC Value -22.22 °C TCC
logP (o/w) 1.85
Solubility
alcohol Yes
water, 3000 mg/L @ 20 °C (exp) Yes

Organoleptic Properties

Odor Type: Chocolate
ethereal, acetone, chocolate
Odor strength medium , recommend smelling in a 1.00 % solution or less
Substantivity < 1 hour(s) at 100.00 %
Luebke, William tgsc, (2007) At 1.00 % in propylene glycol. ethereal acetone chocolate
Flavor Type: Cocoa
ethereal, green, cocoa, nutty, almond, coffee
Luebke, William tgsc, (2007) Ethereal green cocoa nutty almond coffee

Occurrences

Potential Uses

Applications
Odor purposes Currant
Flavoring purposes Bread, Butter, Caramel, Chicken, Chocolate cocoa, Coffee, Mint, Tea, Tomato

Safety Information

Safety information

Preferred SDS: View
European information :
Most important hazard(s):
T - Toxic.
R 11 - Highly flammable.
R 23 - Toxic by inhalation.
S 07/09 - Keep container tightly closed and in well-ventilated place.
S 16 - Keep away from sources of ignition - No Smoking.
S 33 - Take precautionary measures against static discharge.
S 36/37/39 - Wear suitable clothing, gloves and eye/face protection.
S 45 - In case of accident or if you feel unwell seek medical advice immediately.
Hazards identification
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
Pictogram
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
inhalation-rat LC50 500 ppm/4H
LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES
American Industrial Hygiene Association Journal. Vol. 50, Pg. A359, 1989.

Safety in use information

Category:
flavoring agents
Recommendation for 2-methyl furan usage levels up to:
not for fragrance use.
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.21 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 0.30 (μg/capita/day)
Structure Class: II
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 22
Click here to view publication 22
average usual ppmaverage maximum ppm
baked goods: 10.0000050.00000
beverages(nonalcoholic): --
beverages(alcoholic): --
breakfast cereal: 5.0000025.00000
cheese: 7.0000035.00000
chewing gum: --
condiments / relishes: 5.0000025.00000
confectionery froastings: 10.0000050.00000
egg products: --
fats / oils: 5.0000025.00000
fish products: 2.0000010.00000
frozen dairy: 7.0000035.00000
fruit ices: 10.0000050.00000
gelatins / puddings: --
granulated sugar: --
gravies: 5.0000025.00000
hard candy: --
imitation dairy: --
instant coffee / tea: --
jams / jellies: 7.0000035.00000
meat products: 20.00000100.00000
milk products: 7.0000035.00000
nut products: --
other grains: 5.0000025.00000
poultry: --
processed fruits: 7.0000035.00000
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: 5.0000025.00000
snack foods: 10.0000050.00000
soft candy: --
soups: 5.0000025.00000
sugar substitutes: --
sweet sauces: --

Safety references

European Food Safety Athority(EFSA):Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...

European Food Safety Authority (EFSA) reference(s):

Scientific Opinion on Flavouring Group Evaluation 13Rev1: Furfuryl and furan derivatives with and without additional side-chain substituents and heteroatoms from chemical group 14
View page or View pdf

Consideration of sulfur-substituted furan derivatives used as flavouring agents evaluated by JECFA (59th meeting) structurally related to a subgroup of substances within the group of “Furfuryl and furan derivatives with and without additional side-chain substituents and heteroatoms from chemical group 14” evaluated by EFSA in FGE.13Rev1 (2009)
View page or View pdf

Flavouring Group Evaluation 67 (FGE.67): Consideration of 40 furan-substituted aliphatic hydrocarbons, alcohols, aldehydes, ketones, carboxylic acids and related esters, sulfides, disulfides and ethers evaluated by JECFA at the 65th meeting (JECFA, 2006b) and re-evaluated at the 69th meeting (JECFA, 2009c)
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 13, Revision 2 (FGE.13Rev2): Furfuryl and furan derivatives with and without additional side-chain substituents and heteroatoms from chemical group 14
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 67, Revision 1 (FGE.67Rev.1): Consideration of 40 furan-substituted aliphatic hydrocarbons, alcohols, aldehydes, ketones, carboxylic acids and related esters, sulfides, disulfides and ethers evaluated by JECFA at the 65th meeting (JECFA, 2006b) and re-evaluated at the 69th meeting (JECFA, 2009c)
View page or View pdf

Statement on List of Representative Substances for Testing. The current Statement lays down a list of substances in sub-groups with representative substances for which additional data are required prior to their evaluation through the Procedure (Regulation (EC) No 1565/2000).
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 67 Revision 2 (FGE.67Rev2): Consideration of 28 furan-substituted compounds evaluated by JECFA at the 55th, 65th and 69th meetings (JECFA, 2001, 2006a, 2009b)
View page or View pdf

Risks for public health related to the presence of furan and methylfurans in food
View page or View pdf

Identifying and collecting relevant literature related to the oral toxicity of furan and its methyl analogues, 2-methylfuran and 3-methylfuran
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 13 Revision 3 (FGE.13Rev3): furfuryl and furan derivatives with and without additional side-chain substituents and heteroatoms from chemical group 14
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 67, Revision 3 (FGE.67Rev3): consideration of 23 furan-substituted compounds evaluated by JECFA at the 55th, 65th, 69th and 86th meetings
View page or View pdf

EPI System: View
Chemical Carcinogenesis Research Information System:Search
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):534-22-5
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :10797
National Institute of Allergy and Infectious Diseases:Data
WISER:UN 2301
WGK Germany:1
2-methylfuran
Chemidplus:0000534225
EPA/NOAA CAMEO:hazardous materials
RTECS:LU2625000 for cas# 534-22-5