rosefuran
3-methyl-2-(3-methylbut-2-en-1-yl)furan
 
Notes:
None found
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CAS Number: 15186-51-3Picture of molecule3D/inchi
FDA UNII: PNC9VDU98G
Nikkaji Web: J14.082A
XlogP3-AA: 3.30 (est)
Molecular Weight: 150.22078000
Formula: C10 H14 O
NMR Predictor: Predict (works with chrome or firefox)
EFSA/JECFA Comments: Register name to be changed to: 3-Methyl-2/(3-methylbut-2-enyl)furan.
Category: flavor and fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
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Perfumer and Flavorist: Search
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US Patents: Search
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NCBI: Search
JECFA Food Flavoring: 1494  3-methyl-2-(3-methylbut-2-enyl)-furan
DG SANTE Food Flavourings: 13.148  3-methyl-2(3-methylbut-2-en-1-yl)furan
FEMA Number: 4174 3-methyl-2-(3-methylbut-2-en-1-yl)furan
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):15186-51-3 ; 3-METHYL-2(3-METHYLBUT-2-EN-1-YL)FURAN
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Physical Properties:
Appearance: colorless clear liquid (est)
Assay: 98.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 0.99800 to 1.00400 @  25.00 °C.
Pounds per Gallon - (est).: 8.304 to  8.354
Refractive Index: 1.47300 to 1.47900 @  20.00 °C.
Boiling Point: 70.00 °C. @ 11.00 mm Hg
Boiling Point: 194.00 to  195.00 °C. @ 760.00 mm Hg
Acid Value: 1.00 max. KOH/g
Vapor Pressure: 0.608000 mmHg @ 25.00 °C. (est)
Flash Point: 144.00 °F. TCC ( 62.22 °C. )
logP (o/w): 3.533 (est)
Soluble in:
 alcohol
 water, 17.32 mg/L @ 25 °C (est)
Insoluble in:
 water
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Organoleptic Properties:
 
Odor Type: caramellic
 
Odor Strength: high ,
recommend smelling in a 1.00 % solution or less
 
 caramellic  green  minty  
Odor Description:
at 1.00 % in dipropylene glycol. 
caramel green minty
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
Parchem
rosefuran
Chemical Sources Association
Need This Item for Flavor/Food?: You can contact the CSA
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Safety Information:
 
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
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Safety in Use Information:
Category: flavor and fragrance agents
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for rosefuran usage levels up to:
  0.6000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.12 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 0.20 (μg/capita/day)
Modified Theoretical Added Maximum Daily Intake (mTAMDI): 470 (μg/person/day)
Threshold of Concern:90 (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: 22
Click here to view publication 22
 average usual ppmaverage maximum ppm
baked goods: 5.0000025.00000
beverages(nonalcoholic): --
beverages(alcoholic): --
breakfast cereal: 2.0000010.00000
cheese: 3.0000015.00000
chewing gum: --
condiments / relishes: 2.0000010.00000
confectionery froastings: 4.0000020.00000
egg products: --
fats / oils: 2.0000010.00000
fish products: 1.000005.00000
frozen dairy: 3.0000015.00000
fruit ices: 3.0000015.00000
gelatins / puddings: --
granulated sugar: --
gravies: --
hard candy: --
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: 1.000005.00000
milk products: 3.0000015.00000
nut products: --
other grains: 2.0000010.00000
poultry: 1.000005.00000
processed fruits: 2.0000010.00000
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: 2.0000010.00000
snack foods: 5.0000025.00000
soft candy: --
soups: 2.0000010.00000
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): 3.5000015.00000
Fats and oils, and fat emulsions (type water-in-oil) (02.0): 1.7000010.00000
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): --
Chewing gum (05.0): --
Cereals and cereal products, incl. flours & starches from roots & tubers, pulses & legumes, excluding bakery (06.0): 1.0000010.00000
Bakery wares (07.0): 1.0000025.00000
Meat and meat products, including poultry and game (08.0): 3.000005.00000
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): --
Alcoholic beverages, incl. alcohol-free and low-alcoholic counterparts (14.2): --
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): --
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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):
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 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
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
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 15186-51-3
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 84825
National Institute of Allergy and Infectious Diseases: Data
 3-methyl-2-(3-methylbut-2-enyl)furan
Chemidplus: 0015186513
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References:
 3-methyl-2-(3-methylbut-2-enyl)furan
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 15186-51-3
Pubchem (cid): 84825
Pubchem (sid): 135040837
Flavornet: 15186-51-3
Pherobase: View
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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): Search
FooDB: FDB009846
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
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Potential Blenders and core components note
 
For Odor
acidic
 cyclohexyl acetic acidFL/FR
balsamic
2-acetyl furanFL/FR
buttery
 acetoinFL/FR
 acetyl propionylFL/FR
3,4-hexane dioneFL/FR
2-oxobutyric acidFL/FR
 caramel furanone solutionFL/FR
 caramel pentadioneFL/FR
 cycloteneFL/FR
 cyclotene hydrateFL/FR
alpha,alpha-dimethyl anisyl acetoneFL/FR
 ethyl 2-hydroxy-2-methyl butyrateFL/FR
 ethyl cyclopentenoloneFL/FR
 ethyl maltolFL/FR
5-ethyl-2,3,4,5-tetramethyl-2-cyclohexen-1-oneFL/FR
 fenugreek absoluteFL/FR
 geranyl crotonateFR
 immortelle absoluteFL/FR
 levulinic acidFL/FR
 maltolFL/FR
 maltyl propionateFL/FR
 maple furanoneFL/FR
 menthone lactoneFL/FR
 mesitene lactoneFR
5-methyl furfuralFL/FR
 shoyu furanoneFL/FR
 strawberry furanoneFL/FR
 strawberry furanone acetateFL/FR
 toffee furanoneFL/FR
citrus
 ocimene quintoxideFL/FR
coconut
gamma-heptalactoneFL/FR
coumarinic
 tonka bean resinoidFR
creamy
gamma-butyrolactoneFL/FR
ethereal
 ethyl 4-pentenoateFL/FR
 ethyl pyruvateFL/FR
isovaleraldehyde propylene glycol acetalFL/FR
fermented
 ethyl (E)-2-crotonateFL/FR
floral
 cyclohexyl propanolFR
 geranium oil chinaFL/FR
fruity
2-cyclopentyl cyclopentanoneFL/FR
1,8-dimethoxy-para-menthane 
(E)-ethyl tiglateFL/FR
 tetrahydrofurfuryl acetateFL/FR
1,3,3,5-tetramethyl-7-carbomethoxybicyclo(2.2.2)octane 
1,3,3,5-tetramethyl-8-carbomethoxybicyclo(2.2.2)octane 
green
isoamyl 3-(2-furan) propionateFL/FR
2-tert-butyl pyrazineFL/FR
1,5-dimethyl-3-isopropyl-2-oxabicyclo(2.2.2)octane 
3-methylthio-4-heptanone 
1,3,3,5-tetramethyl-8-carbomethoxybicyclo(2.2.2)oct-5-ene 
herbal
 barosma betulina leaf oilFL/FR
 butyl levulinateFL/FR
 cajuput oil replacerFR
 dehydroxylinalool oxideFL/FR
 melaleuca leucadendron cajaputi oilFL/FR
licorice
sweet basil oleoresinFL/FR
minty
 agathosma crenulata leaf oilFL/FR
 mentha longifolia oilFR
 peppermint absoluteFL/FR
isopropyl tiglateFL/FR
isopulegyl formateFL/FR
 spearmint absoluteFL/FR
 spearmint oil americaFL/FR
musty
3-acetyl-2,5-dimethyl furanFL/FR
nutty
2-acetyl-3,5(or 6)-dimethyl pyrazineFL/FR
2,3-dimethyl pyrazineFL/FR
 nutty cyclohexenoneFL/FR
phenolic
4-methyl-2,6-dimethoxyphenolFL/FR
sweet marjoram oil replacerFR
 origanum majorana oilFL/FR
(E)-tiglic acidFL/FR
sulfurous
 buchu mercaptanFL/FR
sweet
 vanilla oleoresin baliFL/FR
tonka
 tonka bean absoluteFR
vanilla
 ethyl vanillinFL/FR
 vanillyl isobutyrateFL/FR
vegetable
 tetrahydrofurfuryl alcoholFL/FR
 
For Flavor
 
No flavor group found for these
2-acetyl-3,4,5,6-tetrahydropyridineFL
 allyl 2-furoateFL
 benzyl disulfideFL
2-tert-butyl pyrazineFL/FR
2-cyclopentyl cyclopentanoneFL/FR
2,5-diethyl tetrahydrofuranFL
alpha,alpha-dimethyl anisyl acetoneFL/FR
 ethyl 2-hydroxy-2-methyl butyrateFL/FR
 ethyl 2-methyl-2-(methyl thio) propionateFL
 ethyl 4-pentenoateFL/FR
5-ethyl-2,3,4,5-tetramethyl-2-cyclohexen-1-oneFL/FR
 furfuryl acetoneFL
 menthone lactoneFL/FR
3-methylthio-4-heptanone 
isopulegyl formateFL/FR
1,3,3,5-tetramethyl-7-carbomethoxybicyclo(2.2.2)octane 
1,3,3,5-tetramethyl-8-carbomethoxybicyclo(2.2.2)oct-5-ene 
1,3,3,5-tetramethyl-8-carbomethoxybicyclo(2.2.2)octane 
isoamyl 3-(2-furan) propionateFL/FR
acidic
 levulinic acidFL/FR
bready
 mango furanoneFL
brown
2-oxobutyric acidFL/FR
5-methyl furfuralFL/FR
 tetrahydrofurfuryl acetateFL/FR
(E)-tiglic acidFL/FR
burnt
 furfuryl alcoholFL
buttery
 diacetylFL
3,4-hexane dioneFL/FR
caramellic
 caramel furanoneFL
 caramel furanone solutionFL/FR
 caramel pentadioneFL/FR
 cycloteneFL/FR
 cyclotene hydrateFL/FR
 ethyl maltolFL/FR
5-ethyl-3,4,5,6-tetramethyl cyclohexen-2-oneFL
 fenugreek absoluteFL/FR
 maltolFL/FR
 maltyl propionateFL/FR
 maple furanoneFL/FR
3-methyl butyl 2-furyl butyrateFL
 shoyu furanoneFL/FR
 strawberry furanoneFL/FR
 strawberry furanone acetateFL/FR
 toffee furanoneFL/FR
citrus
1,5-dimethyl-3-isopropyl-2-oxabicyclo(2.2.2)octane 
coffee
2-isopropyl pyrazineFL
2-thiophene thiolFL
creamy
 acetoinFL/FR
fatty
2,4-undecadienalFL
(E,E)-2,4-undecadienalFL
floral
 geranium oil chinaFL/FR
fruity
(E)-ethyl tiglateFL/FR
 furfuryl valerateFL
2-pentanoyl furanFL
isovaleraldehyde propylene glycol acetalFL/FR
green
 immortelle absoluteFL/FR
 ocimene quintoxideFL/FR
isopropyl tiglateFL/FR
herbal
 barosma betulina leaf oilFL/FR
 butyl levulinateFL/FR
5-hydroxymethyl furfuralFL
 melaleuca leucadendron cajaputi oilFL/FR
 origanum majorana oilFL/FR
jammy
 ethyl cyclopentenoloneFL/FR
lactonic
gamma-heptalactoneFL/FR
licorice
sweet basil oleoresinFL/FR
milky
gamma-butyrolactoneFL/FR
minty
 agathosma crenulata leaf oilFL/FR
 peppermint absoluteFL/FR
 spearmint absoluteFL/FR
 spearmint oil americaFL/FR
musty
 ethyl (E)-2-crotonateFL/FR
nutty
2-acetyl furanFL/FR
3-acetyl-2,5-dimethyl furanFL/FR
2-acetyl-3,5(or 6)-dimethyl pyrazineFL/FR
1,8-dimethoxy-para-menthane 
2,3-dimethyl pyrazineFL/FR
 nutty cyclohexenoneFL/FR
 peanut oxazoleFL
 tetrahydrofurfuryl alcoholFL/FR
phenolic
4-methyl-2,6-dimethoxyphenolFL/FR
rummy
 ethyl pyruvateFL/FR
sulfurous
 buchu mercaptanFL/FR
sweet
 caramel dioneFL
 cyclohexyl acetic acidFL/FR
 vanilla oleoresin baliFL/FR
toasted
 acetyl propionylFL/FR
vanilla
 ethyl vanillinFL/FR
 vanillyl isobutyrateFL/FR
waxy
 furfuryl octanoateFL
woody
 dehydroxylinalool oxideFL/FR
 
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Potential Uses:
 caramelFL
 mintFR
 roseFR
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Occurrence (nature, food, other): note
 cactus vanilla cactus
Search Trop  Picture
 ginger rhizome
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 ginger rhizome oil
Search Trop  Picture
 rebutia marsoneri
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 rose oil
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Synonyms:
gamma-clausenane
 furan, 3-methyl-2-(3-methyl-2-butenyl)-
(methyl butenyl) methyl furan
3-methyl-2-(3-methyl but-2-en-1-yl) furan
3-methyl-2-(3-methyl-2-butenyl) furan
3-methyl-2-(3-methylbut-2-en-1-yl)furan
3-methyl-2-(3-methylbut-2-enyl)-furan
3-methyl-2-(3-methylbut-2-enyl)furan
2-(3-methyl-2-butenyl)-3-methyl furan
2-(3-methyl-2-butenyl)-3-methylfuran
3-methyl-2-prenylfuran
2-(3'-methyl-2'-butenyl)-3-methylfuran
3-methyl-2(3-methylbut-2-en-1-yl)furan
(methylbutenyl)methylfuran
a-naginatene
alpha-naginatene
 rose furan
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Articles:
Info: substances containing furan substitution
PubMed: From simple furans to complex nitrogen-bearing aromatic polycycles by means of a flexible and general reaction sequence initiated by singlet oxygen.
PubMed: Cellulase production from spent lignocellulose hydrolysates by recombinant Aspergillus niger.
PubMed: Acid-promoted cyclization reactions of tetrahydroindolinones. Model studies for possible application in a synthesis of selaginoidine.
PubMed: Characterization and semiquantitative analysis of volatiles in seedless watermelon varieties using solid-phase microextraction.
PubMed: Triflic anhydride mediated cyclization of 5-hydroxy-substituted pyrrolidinones for the preparation of alpha-trifluoromethylsulfonamido furans.
PubMed: Several convenient methods for the synthesis of 2-amido substituted furans.
PubMed: A pharmacokinetic model for estimating exposure of Americans to dioxin-like compounds in the past, present, and future.
PubMed: Structural elucidation of twelve novel esters composed of five fatty acids and three new branched alcohols together with four monoterpenoids from Sancassania shanghaiensis (Acari: Acaridae).
PubMed: Similarities in the aroma chemistry of Gewürztraminer variety wines and lychee (Litchi chinesis sonn.) fruit.
PubMed: The volatile constituents of Elsholtzia flava.
PubMed: Correlation between dioxin levels in adipose tissue and estimated exposure to Agent Orange in south Vietnamese residents.
PubMed: Some prevalent biomolecules as defenses against singlet oxygen damage.
PubMed: The Essential Oil of Perilla ocimoides: A Rich Source of Rosefuran.
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