(E)-spicy acrolein
trans-3-furan-2-yl-2-phenylprop-2-enal
 
Notes:
None found
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CAS Number: 65545-81-5Picture of molecule3D/inchi
FDA UNII: CHD146V2O2
Nikkaji Web: J775.728J
MDL: MFCD00036566
CoE Number: 11928
XlogP3-AA: 2.50 (est)
Molecular Weight: 198.22110000
Formula: C13 H10 O2
NMR Predictor: Predict (works with chrome or firefox)
Category: flavoring agents
 
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JECFA Food Flavoring: 1502  trans-2-phenyl-3-(2-furyl)prop-2-enal
DG SANTE Food Flavourings: 13.137  (E)-3-(2-furyl)-2-phenylprop-2-enal
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Physical Properties:
Appearance: white solid (est)
Assay: 99.00 to 100.00 % 
Food Chemicals Codex Listed: No
Melting Point: 56.00 to  57.00 °C. @ 760.00 mm Hg
Boiling Point: 326.00 to  327.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.000211 mmHg @ 25.00 °C. (est)
Flash Point: 304.00 °F. TCC ( 151.11 °C. )
logP (o/w): 3.907 (est)
Soluble in:
 alcohol
 water, 134.7 mg/L @ 25 °C (est)
Insoluble in:
 water
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Organoleptic Properties:
Odor Description:
berry
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
Parchem
(E)-furfurylidene phenyl acetaldehyde
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: flavoring agents
Recommendation for (E)-spicy acrolein usage levels up to:
 not for fragrance use.
 
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Safety References:
European Food Safety Authority (EFSA) reference(s):
Scientific Opinion on Flavouring Group Evaluation 222 (FGE.222): Consideration of genotoxicity data on representatives for alpha,beta-unsaturated furyl derivatives with the a,ß-unsaturation in the side chain from subgroup 4.6 of FGE.19 by EFSA
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): 65545-81-5
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 6435876
National Institute of Allergy and Infectious Diseases: Data
 (E)-3-furan-2-yl-2-phenylprop-2-enal
Chemidplus: 0065545815
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References:
 (E)-3-furan-2-yl-2-phenylprop-2-enal
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 6435876
Pubchem (sid): 135019836
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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
HMDB (The Human Metabolome Database): Search
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
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Potential Blenders and core components note
 
For Odor
acidic
2-ethyl butyric acidFL/FR
alliaceous
 methyl furfuryl disulfideFL/FR
amber
 ambrette seed absoluteFL/FR
balsamic
 conifer acetateFR
 fir balsam absoluteFR
 methyl (E)-cinnamateFL/FR
berry
 raspberry ketone acetateFL/FR
caramellic
 maltyl isobutyrateFL/FR
 strawberry furanoneFL/FR
earthy
3-octen-2-oneFL/FR
ethereal
 propyl formateFL/FR
floral
beta-damascenoneFL/FR
 heliotropyl acetoneFL/FR
beta-iononeFL/FR
beta-ionyl acetateFL/FR
 rose carboxylateFR
 tetrahydroionyl acetateFR
fruity
 allyl benzoateFR
isoamyl 2-methyl butyrateFL/FR
 artemisia pallens herb oilFL/FR
3-benzyl-4-heptanoneFL/FR
 berry pentadienoateFL/FR
isobutyl anthranilateFL/FR
 butyl hexanoateFL/FR
 butyl valerateFL/FR
 ethyl levulinateFL/FR
 ethyl methyl-para-tolyl glycidateFL/FR
 ethyl valerateFL/FR
 geranyl isovalerateFL/FR
 methyl beta-ionolFR
 methyl propionateFL/FR
3-nonen-2-oneFL/FR
 octyl propionateFL/FR
 osmanthus flower absoluteFL/FR
3-phenyl propyl isovalerateFL/FR
isopropenyl acetateFL/FR
isopropyl hexanoateFL/FR
 prune glycidateFR
 strawberry glycidate 1 (aldehyde C-16 (so-called))FL/FR
4-(para-tolyl)-2-butanoneFL/FR
 vanilla carboxylateFL/FR
green
 hexyl isobutyrateFL/FR
 hexyl octanoateFL/FR
herbal
 artemisyl ketoneFL/FR
(S)-campholene acetateFL/FR
isodihydrolavandulalFL/FR
 herbal undecanoneFR
jammy
 ethyl 2-methyl-2-pentenoateFR
nutty
2-methyl-3-pentenoic acidFL/FR
sulfurous
 blackberry thiophenoneFL/FR
 buchu mercaptanFL/FR
 mango thiolFL/FR
2-phenethyl isothiocyanateFL/FR
woody
 juniper berry oleoresinFL/FR
 
For Flavor
 
No flavor group found for these
 artemisyl ketoneFL/FR
 blackberry thiophenoneFL/FR
 methyl (E)-cinnamateFL/FR
2-methyl-3-pentenoic acidFL/FR
2-phenethyl isothiocyanateFL/FR
3-phenyl propyl isovalerateFL/FR
isopropyl hexanoateFL/FR
acidic
2-ethyl butyric acidFL/FR
berry
 heliotropyl acetoneFL/FR
 raspberry ketone acetateFL/FR
caramellic
 strawberry furanoneFL/FR
coffee
 methyl furfuryl disulfideFL/FR
creamy
 acetoin butyrateFL
3-octen-2-oneFL/FR
estery
 octyl propionateFL/FR
ethereal
isopropenyl acetateFL/FR
isoamyl 2-methyl butyrateFL/FR
 artemisia pallens herb oilFL/FR
3-benzyl-4-heptanoneFL/FR
 berry pentadienoateFL/FR
isobutyl anthranilateFL/FR
 butyl hexanoateFL/FR
 butyl valerateFL/FR
 ethyl levulinateFL/FR
 ethyl methyl-para-tolyl glycidateFL/FR
 ethyl valerateFL/FR
 furfuryl isovalerateFL
 methyl propionateFL/FR
 osmanthus flower absoluteFL/FR
 propyl formateFL/FR
 strawberry glycidate 1 (aldehyde C-16 (so-called))FL/FR
4-(para-tolyl)-2-butanoneFL/FR
 vanilla carboxylateFL/FR
green
 geranyl isovalerateFL/FR
 hexyl isobutyrateFL/FR
 hexyl octanoateFL/FR
herbal
isodihydrolavandulalFL/FR
jammy
(S)-campholene acetateFL/FR
 maltyl isobutyrateFL/FR
oily
3-nonen-2-oneFL/FR
sulfurous
 buchu mercaptanFL/FR
 mango thiolFL/FR
woody
 ambrette seed absoluteFL/FR
beta-damascenoneFL/FR
beta-iononeFL/FR
beta-ionyl acetateFL/FR
 juniper berry oleoresinFL/FR
 
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Potential Uses:
 berry mixed berryFL
 fruitFR
 raspberryFL
 strawberryFL
 tropicalFL
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
(E)-3-furan-2-yl-2-phenylprop-2-enal
trans-3-furan-2-yl-2-phenylprop-2-enal
(E)-furfurylidene phenyl acetaldehyde
trans-furfurylidene phenyl acetaldehyde
(E)-furfurylidenephenylacetaldehyde
trans-furfurylidenephenylacetaldehyde
(E)-3-(2-furyl)-2-phenyl prop-2-enal
trans-3-(2-furyl)-2-phenyl prop-2-enal
(E)-3-(2-furyl)-2-phenyl-2-propenal
trans-3-(2-furyl)-2-phenyl-2-propenal
(E)-3-(2-furyl)-2-phenylprop-2-enal
trans-3-(2-furyl)-2-phenylprop-2-enal
(E)-2-phenyl-3-(2-furyl) prop-2-enal
trans-2-phenyl-3-(2-furyl) prop-2-enal
(E)-2-phenyl-3-(2-furyl)-2-propenal
trans-2-phenyl-3-(2-furyl)-2-propenal
(E)-2-phenyl-3-(2-furyl)prop-2-enal
trans-2-phenyl-3-(2-furyl)prop-2-enal
trans-spicy acrolein
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