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ethyl 3-(2-furyl) propanoate

Ethyl 3-(2-furyl) propanoate is a flavor and fragrance compound known for its sweet, fruity pineapple odor and use in food and beverage formulations.
Chemical Structure

General Material Description

Ethyl 3-(2-furyl) propanoate is an organic ester with the molecular formula C9H12O3. It appears as a clear liquid and is characterized by a sweet, fruity aroma reminiscent of pineapple with balsamic undertones. This compound belongs to the class of furan esters and is known under several synonyms including ethyl 2-furanpropanoate and emanol. It is referenced in chemical databases such as PubChem and is typically synthesized or isolated for use in flavor and fragrance formulations. Sourced mainly through synthetic routes, ethyl 3-(2-furyl) propanoate is prized for its tropical and fruity notes that enhance food products and perfumes.

Occurrence, Applicability & Potential Uses

Ethyl 3-(2-furyl) propanoate occurs naturally in certain alcoholic beverages such as rum, contributing to its complex aroma profile. Its applicability spans flavor and fragrance industries where it is employed to impart fruity, pineapple-like notes with subtle balsamic and spicy nuances. The compound’s inclusion is regulated under standards such as FEMA (US), with FEMA number 2435 confirming its recognition as a flavoring substance. It also complies with IFRA (Global) guidelines that recommend usage limits in fragrance concentrates, ensuring safe incorporation into consumer products. Potential uses extend to enhancing citrus, fruit punch, mango, and horseradish flavor profiles, as well as adding amber, chamomile, floral, and woody nuances in perfumes.

Physico-Chemical Properties Summary

Ethyl 3-(2-furyl) propanoate melts between 24 and 25°C and boils at approximately 120 to 121°C under reduced pressure (17 mm Hg). It has a molecular weight of about 168.2 g/mol and a logP estimated at 2.015, indicating moderate lipophilicity. The vapor pressure at 25°C is low (0.148 mmHg), suggesting modest volatility suitable for sustained aroma release in formulations. Slight water solubility and good solubility in alcohols make it compatible with varied product matrices. The flash point around 91°C (196°F) reflects its moderate flammability. These properties influence its use in complex flavor blends and aroma formulations, balancing volatility and persistence.

FAQ

What is ethyl 3-(2-furyl) propanoate and what are its main characteristics?
Ethyl 3-(2-furyl) propanoate is a furan-based ester compound primarily used as a flavor and fragrance agent. It exhibits a sweet, fruity aroma reminiscent of pineapple with balsamic and slightly spicy undertones. The compound appears as a clear liquid with the molecular formula C9H12O3 and a molecular weight of approximately 168.2 g/mol. It is known by several synonyms, including ethyl 2-furanpropanoate and emanol. Its sensory qualities make it valuable in enhancing fruity and tropical flavor profiles.
Where does ethyl 3-(2-furyl) propanoate occur naturally, and how is it applied in industry?
Ethyl 3-(2-furyl) propanoate naturally occurs in some alcoholic beverages such as rum, contributing to their distinctive aroma. Industrially, it is synthesized and applied in flavor and fragrance formulations to impart fruity and tropical notes including pineapple, mango, and citrus characteristics. Its use extends to adding amber, chamomile, floral, woody, and balsamic nuances in perfumes. Its solubility properties and volatility make it suitable for incorporation into both food and cosmetic products.
What regulations and safety considerations apply to ethyl 3-(2-furyl) propanoate in food and fragrances?
Ethyl 3-(2-furyl) propanoate is regulated under standards such as FEMA (US) where it holds FEMA number 2435 and is recognized as a safe flavoring substance when used within specified limits. The International Fragrance Association (IFRA, Global) recommends usage levels up to 0.5% in fragrance concentrates to ensure consumer safety. Safety data indicate it may cause irritation to eyes, skin, and respiratory system, requiring appropriate handling precautions. It is classified as harmful (Xn) under European regulations, and users should follow safety guidelines such as wearing protective equipment and avoiding ingestion or inhalation during handling.

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

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Literature & References

ethyl 3-furan-2-ylpropanoate
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:10031-90-0
Pubchem (cid):61450
Pubchem (sid):135017163
Publications by Info
substances containing furan substitution
Publications by US Patents
3,952,024 - Furfurylthioacetone
Flavoring agent

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
HMDB (The Human Metabolome Database):HMDB32921
FooDB:FDB010904
Export Tariff Code:2932.19.0002
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

General Material Information

Preferred name ethyl 3-(2-furyl) propanoate
Trivial Name Ethyl 2-furanpropanoate
Short Description ethyl 3-(2-furyl)propanoate
Formula C9 H12 O3
CAS Number 10031-90-0
FEMA Number 2435
Flavis Number 13.022
ECHA Number 233-097-5
FDA UNII 2RAP445QD8
Nikkaji Number J241.236E
MDL MFCD00036496
COE Number 2091
Bio Activity Summary External link
NMR Predictor External link
JECFA Food Flavoring 1513 ethyl 3-(2-furyl)propanoate
FDA Patent No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm 10031-90-0 ; ETHYL 2-FURANPROPIONATE
Synonyms
  • emanol
  • ethyl 2-furan propanoate
  • ethyl 2-furan propionate
  • ethyl 2-furanpropanoate
  • ethyl 2-furanpropionate
  • ethyl 3-(.alpha.-furyl)-propionate
  • ethyl 3-(2-furyl) propionate
  • ethyl 3-(2-furyl)propanoate
  • ethyl 3-(2-furyl)propionate
  • ethyl 3-(a-furyl)propionate
  • ethyl 3-(alpha-furyl) propionate
  • ethyl 3-(furan-2-yl)propanoate
  • ethyl 3-furan-2-ylpropanoate
  • ethyl 3(2-furyl) propanoate
  • ethyl 3(2-furyl)propanoate
  • ethyl beta-furyl propionate
  • ethyl furan-2-propionate
  • ethyl furyl propionate
  • 2-furan propanoic acid ethyl ester
  • 2-furan propionic acid ethyl ester
  • furan-2-propionic acid ethyl ester
  • 2-furanepropanoic acid ethyl ester
  • 2-furanpropanoic acid, ethyl ester
  • 2-furanpropionic acid, ethyl ester
  • 3-(2-furyl)propionic acid ethyl ester
  • 2-Furanpropanoic acid, ethyl ester
  • 2-Furanpropionic acid, ethyl ester
  • Ethyl β-furylpropionate
  • Ethyl 3-(α-furyl)propionate
  • NSC 97529
  • Ethyl 3-(furan-2-yl)propionate

PhysChem Properties

Material listed in food chemical codex No
Molecular weight 168.1922454834
Melting Point 24 to 25°C @ 760 mm Hg
Boiling Point 120 to 121°C @ 17 mm Hg
Acid Value 5 max KOH/g
Vapor Pressure 0.148 mmHg @ 25 °C
Vapor Density 1
Flash Point TCC Value 91.11 °C TCC
logP (o/w) 2.015 est
Solubility
alcohol Yes
water, very slightly Yes
water, 524.5 mg/L @ 25 °C (est) Yes
water No

Organoleptic Properties

Odor Type: Fruity
sweet, fruity, pineapple, balsamic, ripe, acrylate, rummy, horseradish, cooked, jammy
Odor strength medium
Substantivity 68 hour(s) at 100.00 %
Luebke, William tgsc, (1986) At 100.00 %. sweet fruity pineapple balsam
Mosciano, Gerard P&F 18, No. 6, 33, (1993) Sweet, fruity, pineapple, ripe, acrylate rumy note, horseradish and slightly cooked jammy nuance
Flavor Type: Fruity
pineapple, fruity, sweet, spicy, tropical, ripe, jammy
Mosciano, Gerard P&F 18, No. 6, 33, (1993) At 15.00 ppm. Pineapple, fruity, sweet slightly spicy, tropical, ripe and slightly jammy
Strong, aged cheese, as well as overripe fruit, particularly pineapple. Strong, aged cheese, overripe fruit especially pineapple

Occurrences

Potential Uses

Applications
Odor purposes Amber , Balsam , Chamomile , Floral , Woody
Flavoring purposes Citrus , Fruit punch , Horseradish , Mango , Pineapple

Safety Information

Safety information

Preferred SDS: View
European information :
Most important hazard(s):
Xn - Harmful.
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 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.
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:
Not determined

Safety in use information

Category:
flavor and fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for ethyl 3-(2-furyl) propanoate usage levels up to:
0.5000 % in the fragrance concentrate.
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.012 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 0.07 (μg/capita/day)
Modified Theoretical Added Maximum Daily Intake (mTAMDI): 1000 (μg/person/day)
Threshold of Concern:90 (μg/person/day)
Structure Class: III
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: -7.50000
beverages(nonalcoholic): -1.60000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -1.60000
fruit ices: -1.60000
gelatins / puddings: --
granulated sugar: --
gravies: --
hard candy: -5.60000
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: --
Food categories according to Commission Regulation EC No. 1565/2000 (EC, 2000) in FGE.06 (EFSA, 2002a). According to the Industry the "normal" use is defined as the average of reported usages and "maximum use" is defined as the 95th percentile of reported usages (EFSA, 2002i).
Note: mg/kg = 0.001/1000 = 0.000001 = 1/1000000 = ppm.
average usage mg/kgmaximum usage mg/kg
Dairy products, excluding products of category 02.0 (01.0): 3.70000-
Fats and oils, and fat emulsions (type water-in-oil) (02.0): --
Edible ices, including sherbet and sorbet (03.0): --
Processed fruit (04.1): --
Processed vegetables (incl. mushrooms & fungi, roots & tubers, pulses and legumes), and nuts & seeds (04.2): --
Confectionery (05.0): 3.75000-
Chewing gum (05.3): --
Cereals and cereal products, incl. flours & starches from roots & tubers, pulses & legumes, excluding bakery (06.0): --
Bakery wares (07.0): 4.26000-
Meat and meat products, including poultry and game (08.0): --
Fish and fish products, including molluscs, crustaceans and echinoderms (MCE) (09.0): --
Eggs and egg products (10.0): --
Sweeteners, including honey (11.0): --
Salts, spices, soups, sauces, salads, protein products, etc. (12.0): --
Foodstuffs intended for particular nutritional uses (13.0): --
Non-alcoholic ("soft") beverages, excl. dairy products (14.1): 0.95000-
Alcoholic beverages, incl. alcohol-free and low-alcoholic counterparts (14.2): 1.00000-
Ready-to-eat savouries (15.0): --
Composite foods (e.g. casseroles, meat pies, mincemeat) - foods that could not be placed in categories 01.0 - 15.0 (16.0): --

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):

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 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

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

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
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):10031-90-0
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :61450
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
ethyl 3-furan-2-ylpropanoate
Chemidplus:0010031900