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General Material Information

Preferred name furfuryl alcohol
Trivial Name Furfuryl alcohol
Short Description 2-furanmethanol
Formula C5 H6 O2
CAS Number 98-00-0
FEMA Number 2491
Flavis Number 13.019
ECHA Number 202-626-1
FDA UNII D582054MUH
Nikkaji Number J3.578E
Beilstein Number 0106291
MDL MFCD00003252
COE Number 2023
Bio Activity Summary External link
NMR Predictor External link
JECFA Food Flavoring 451 furfuryl alcohol
FDA Patent No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm 98-00-0 ; FURFURYL ALCOHOL
Synonyms
  • 2-furan carbinol
  • 2-furan methanol
  • furan-2-ylmethanol
  • 2-furancarbinol
  • 2-furanmethanol
  • 2-furanyl methanol
  • 2-furanylmethanol
  • furfural alcohol
  • furfuralcohol
  • furfuranol
  • 2-furfuryl alcohol
  • furfuryl alcohol natural
  • furfuryl alcohol synthetic
  • furfuryl carb
  • furfurylalcohol
  • 2-furfurylalkohol
  • furfurylcarb
  • furyl carbinol
  • 2-furyl carbinol
  • alpha- furyl carbinol
  • 2-furyl methanol
  • 2-furylcarbinol
  • a- furylcarbinol
  • 2-furylmethan-1-ol
  • 2-furylmethanol
  • 2-hydroxymethyl furan
  • 5-hydroxymethyl furan
  • 2-( hydroxymethyl)furan
  • 5-hydroxymethylfuran
  • methanol, (2-furyl)-
  • 2-Furanmethanol
  • 2-Furancarbinol
  • α-Furylcarbinol
  • 2-Furylcarbinol
  • Furylcarbinol
  • 2-Furfuryl alcohol
  • 2-(Hydroxymethyl)furan
  • 5-Hydroxymethylfuran
  • α-Furfuryl alcohol
  • 2-Furylmethanol
  • 2-Furanylmethanol
  • Chem-Rez 200
  • NSC 8843
  • 2-Furylmethyl alcohol
  • Chem-Rez Fury 454

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

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Literature & References

furan-2-ylmethanol
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:98-00-0
Pubchem (cid):7361
Pubchem (sid):134970818
Flavornet:98-00-0
Pherobase:View
Publications by PubMed
Identification of 2-ethyl-4-methyl-3-thiazoline and 2-isopropyl-4-methyl-3-thiazoline for the first time in nature by the comprehensive analysis of sesame seed oil.
Role of roasting conditions in the profile of volatile flavor chemicals formed from coffee beans.
Physicochemical model to interpret the kinetics of aroma extraction during wine aging in wood. Model limitations suggest the necessary existence of biochemical processes.
Aroma compounds in sweet whey powder.
Influence of the brewing process on furfuryl ethyl ether formation during beer aging.
Furfuryl ethyl ether: important aging flavor and a new marker for the storage conditions of beer.
Volatile flavor components of stored nonfat dry milk.
Volatile flavor components of rice cakes.
Changes in chemical composition of frozen coated fish products during deep-frying.
Formation of cysteine-S-conjugates in the Maillard reaction of cysteine and xylose.
Effect of Saccharomyces strains on the quality of red wines aged on lees.
Volatile profiling of high quality hazelnuts (Corylus avellana L.): chemical indices of roasting.
Impact of cooking and handling conditions on furanic compounds in breaded fish products.
Characterisation of bound volatile compounds of a low flavour kiwifruit species: Actinidia eriantha.
Effects of alcohol compounds on the growth and lipid accumulation of oleaginous yeast Trichosporon fermentans.
Quantification of furanic compounds in coated deep-fried products simulating normal preparation and consumption: optimisation of HS-SPME analytical conditions by response surface methodology.
Characterization of the polymerization of furfuryl alcohol during roasting of coffee.
In vivo detoxification of furfural during lipid production by the oleaginous yeast Trichosporon fermentans.
Effects of Litchi chinensis fruit isolates on prostaglandin E(2) and nitric oxide production in J774 murine macrophage cells.
Evaluation of certain food additives.
The potential of biodetoxification activity as a probiotic property of Lactobacillus reuteri.
Degradation of 5-hydroxymethylfurfural during yeast fermentation.
Hydroxymethyl-substituted furans: mutagenicity in Salmonella typhimurium strains engineered for expression of various human and rodent sulphotransferases.
Identification of 2-ethyl-4-methyl-3-thiazoline and 2-isopropyl-4-methyl-3-thiazoline for the first time in nature by the comprehensive analysis of sesame seed oil.
Use of microfungi in the treatment of oak chips: possible effects on wine.
Role of roasting conditions in the profile of volatile flavor chemicals formed from coffee beans.
Monitoring cytotoxic potentials of furfuryl alcohol and 2-furyl methyl ketone in mice.
Sisal fibers: surface chemical modification using reagent obtained from a renewable source; characterization of hemicellulose and lignin as model study.
Influence of epicatechin reactions on the mechanisms of Maillard product formation in low moisture model systems.
Photosensitizing properties of protein hydrolysate-based fertilizers.
Difference in the volatile composition of pine-mushrooms (Tricholoma matsutake Sing.) according to their grades.
Physicochemical model to interpret the kinetics of aroma extraction during wine aging in wood. Model limitations suggest the necessary existence of biochemical processes.
5-(Hydroxymethyl)-2-furfural: a selective inhibitor of DNA polymerase lambda and terminal deoxynucleotidyltransferase.
Comparison of estimated daily intakes of flavouring substances with no-observed-effect levels.
Influence of the brewing process on furfuryl ethyl ether formation during beer aging.
Furfuryl ethyl ether: important aging flavor and a new marker for the storage conditions of beer.
Volatile compounds in a spanish red wine aged in barrels made of Spanish, French, and American oak wood.
Extraction and formation dynamic of oak-related volatile compounds from different volume barrels to wine and their behavior during bottle storage.
Volatile flavor components of stored nonfat dry milk.
Formation and Degradation of Furfuryl Alcohol, 5-Methylfurfuryl Alcohol, Vanillyl Alcohol, and Their Ethyl Ethers in Barrel-Aged Wines.
Effect of alcohol compounds found in hemicellulose hydrolysate on the growth and fermentation of ethanologenic Escherichia coli.
Volatile flavor components of rice cakes.
NTP Toxicology and Carcinogenesis Studies of Furfural (CAS No. 98-01-1) in F344/N Rats and B6C3F1 Mice (Gavage Studies).

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
FDA Indirect Additives used in Food Contact Substances:View
CHEBI:View
CHEMBL:View
UM BBD:Search
KEGG (GenomeNet):C20441
HMDB (The Human Metabolome Database):HMDB13742
FooDB:FDB012558
Export Tariff Code:2932.13.0000
Typical G.C.
VCF-Online:VCF Volatile Compounds in Food
ChemSpider: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
Formulations/Preparations:
grade: technical, refined.

PhysChem Properties

Material listed in food chemical codex No
Molecular weight 98.101219177246
Specific gravity @ 25 °C
Pounds per Gallon 9.386 to 9.461
Refractive Index 1.476 to 1.487 @ 20 °C
Melting Point -29 to -28°C @ 760 mm Hg
Boiling Point 169 to 171°C @ 760 mm Hg
Boiling Point 96 to 97°C @ 50 mm Hg
Vapor Pressure 1.009 mmHg @ 25 °C
Vapor Density 3.4
Flash Point TCC Value 65 °C TCC
logP (o/w) 0.28
Shelf life 12 months (or longer if stored properly.)
Storage notes Store in cool, dry place in tightly sealed containers, protected from heat and light.
Solubility
alcohol Yes
water, 2.21e+005 mg/L @ 25 °C (est) Yes

Organoleptic Properties

Odor Type: Bready
alcoholic, chemical, musty, sweet, caramellic, bready, coffee, sulfurous, estery, brown
Odor strength medium
Substantivity 44 hour(s) at 100.00 %
Luebke, William tgsc, (1997) At 100.00 %. alcoholic chemical musty sweet caramel bread coffee
Mosciano, Gerard P&F 15, No. 2, 69, (1990) Sulfuraceous estery chemical, musty, sweet, brown caramellic, bready and coffee
Flavor Type: Burnt
burnt, sweet, caramellic, brown
Mosciano, Gerard P&F 15, No. 2, 69, (1990) At 50.00 ppm. Burnt, sweet, caramellic, brown

Occurrences

Potential Uses

Applications
Odor purposes Hawthorn
Flavoring purposes Bacon, Beer, Brandy, Bread, Caramel, Chocolate cocoa, Coffee, Malt, Molasses, Sugar brown sugar
Cosmetic purposes Not used anymore

Safety Information

Safety information

Preferred SDS: View
European information :
Most important hazard(s):
Xn - Harmful.
R 20/21/22 - Harmful by inhalation, in contact with skin and if swallowed.
R 36/37/38 - Irritating to eyes, respiratory system, and skin.
S 02 - Keep out of the reach of children.
S 20/21 - When using do not eat, drink or smoke.
S 23 - Do not breath vapour.
S 24/25 - Avoid contact with skin and eyes.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 36/37/39 - Wear suitable clothing, gloves and eye/face protection.
S 36/37/39 - Wear suitable clothing, gloves and eye/face protection.
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:
oral-rat LD50 177 mg/kg
LUNGS, THORAX, OR RESPIRATION: CYANOSIS BEHAVIORAL: EXCITEMENT BEHAVIORAL: ATAXIA
Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 55(6), Pg. 73, 1990.

intraperitoneal-rat LD50 650 mg/kg
Raw Material Data Handbook, Vol.1: Organic Solvents, 1974. Vol. 1, Pg. 64, 1974.

intravenous-rabbit LD50 650 mg/kg
Federation Proceedings, Federation of American Societies for Experimental Biology. Vol. 8, Pg. 294, 1949.

oral-mammal (species unspecified) LD50 360 mg/kg
Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 39(4), Pg. 86, 1974.

oral-mouse LD50 160 mg/kg
Biochemical Journal. Vol. 34, Pg. 1196, 1940.

unreported-mouse LD50 338 mg/kg
Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 55(6), Pg. 73, 1990.

unreported-rabbit LD50 632 mg/kg
Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 55(6), Pg. 73, 1990.

Dermal Toxicity:
skin-rabbit LD50 400 mg/kg
BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD
"Toxicology of Drugs and Chemicals," Deichmann, W.B., New York, Academic Press, Inc., 1969Vol. -, Pg. 280, 1969.

subcutaneous-rat LD50 85 mg/kg
BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD
"Toxicology of Drugs and Chemicals," Deichmann, W.B., New York, Academic Press, Inc., 1969Vol. -, Pg. 280, 1969.

skin-rat LD50 3825 mg/kg
Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 25(9), Pg. 52, 1981.

Inhalation Toxicity:
inhalation-rat LC50 233 ppm/4H
American Industrial Hygiene Association Journal. Vol. 19, Pg. 91, 1958.

inhalation-mouse LCLo 597 ppm/6H
"Toxicology of Drugs and Chemicals," Deichmann, W.B., New York, Academic Press, Inc., 1969Vol. -, Pg. 280, 1969.

Safety in use information

Category:
flavoring agents
IFRA Critical Effect:
Insufficient data
View the IFRA Standard
Recommendation for furfuryl alcohol usage levels up to:
PROHIBITED: Should not be used as a fragrance ingredient.
Maximised Survey-derived Daily Intakes (MSDI-EU): 180.00 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 24.00 (μg/capita/day)
Threshold of Concern:540 (μg/person/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: 3
Click here to view publication 3
average usual ppmaverage maximum ppm
baked goods: -110.00000
beverages(nonalcoholic): -19.00000
beverages(alcoholic): -10.00000
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -88.00000
fruit ices: -88.00000
gelatins / puddings: --
granulated sugar: --
gravies: --
hard candy: -59.00000
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: --
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: --
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):

Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) related to Flavouring Group Evaluation 13 (FGE.13); Furfuryl and furan derivatives with and without additional side-chain substituents and heteroatoms from chemical group 14 (Commission Regulation (EC) No 1565/2000 of 18
View page or View pdf

Flavouring Group Evaluation 66 (FGE.66)[1]:Consideration of furfuryl alcohol and related flavouring substances evaluated by JECFA (55th meeting) structurally related to Furfuryl and furan derivatives with and without additional side chain substituents and heteroatoms evaluated by EFSA in FGE.13 (2005)
View page or View pdf

Flavouring Group Evaluation 218: alpha,beta-Unsaturated aldehydes and precursors from subgroup 4.2 of FGE.19: Furfural derivatives - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food (AFC)
View page or View pdf

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 218, Revision 1 (FGE.218Rev1): alpha,beta-Unsaturated aldehydes and precursors from subgroup 4.2 of FGE.19: Furfural derivatives.
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 66, Revision 1 (FGE.66Rev1): Consideration of Furfuryl Alcohol and Related Flavouring Substances Evaluated by JECFA (55th meeting)
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

Safety and efficacy of furfuryl and furan derivatives belonging to chemical group 14 when used as flavourings for all animal species and categories
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

EPI System: View
NIOSH International Chemical Safety Cards:search
NIOSH Pocket Guide:search
Chemical Carcinogenesis Research Information System:Search
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
Carcinogenic Potency Database:Search
EPA GENetic TOXicology:Search
EPA Substance Registry Services (TSCA):98-00-0
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :7361
National Institute of Allergy and Infectious Diseases:Data
WISER:UN 2874
WGK Germany:1
furan-2-ylmethanol
Chemidplus:0000098000
EPA/NOAA CAMEO:hazardous materials
RTECS:98-00-0