2-phenyl-2-pentenal
benzeneacetaldehyde, a-propylidene-

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  2-Phenyl-2-pentenal Halal, Kosher

Name: 2-phenylpent-2-enal CAS Number: 3491-63-2 3D/inchi FDA UNII: Search MDL: MFCD00051835 XlogP3-AA: 2.60 (est) Molecular Weight: 160.21584000 Formula: C11 H12 O NMR Predictor: Predict (works with chrome, Edge or firefox) Category: flavor and fragrance agents   US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information: Google Scholar: Search Google Books: Search Google Scholar: with word "volatile" Search Google Scholar: with word "flavor" Search Google Scholar: with word "odor" Search Perfumer and Flavorist: Search Google Patents: Search US Patents: Search EU Patents: Search Pubchem Patents: Search PubMed: Search NCBI: Search DG SANTE Food Flavourings: 05.175 2-phenylpent-2-enal   Physical Properties: Appearance: colorless clear liquid (est) Assay: 95.00 to 100.00 sum of isomers Food Chemicals Codex Listed: No Specific Gravity: 1.00500 to 1.01500 @ 25.00 °C. Pounds per Gallon - (est).: 8.363 to 8.446 Refractive Index: 1.54500 to 1.55300 @ 20.00 °C. Boiling Point: 136.00 °C. @ 30.00 mm Hg Boiling Point: 124.00 to 126.00 °C. @ 14.00 mm Hg Vapor Pressure: 0.003000 mmHg @ 25.00 °C. (est) Flash Point: > 212.00 °F. TCC ( > 100.00 °C. ) logP (o/w): 3.207 (est) Soluble in:   alcohol   water, 248.3 mg/L @ 25 °C (est) Insoluble in:   water   Organoleptic Properties: Odor Type: floral Odor Strength:medium Substantivity: > 114 hour(s) at 100.00 % floral hyacinth green narcissus foliage radish honey sweet pea Odor Description:at 100.00 %. floral hyacinth green narcissus foliage radish honey sweet pea Luebke, William tgsc, (2009) Odor sample from: R C Treatt and Co Ltd Flavor Type: green green floral chrysanthemum spicy radish hyacinth foliage honey Taste Description: green floral chrysanthemum spicy radish hyacinth foliage honey Luebke, William tgsc, (2009) Odor and/or flavor descriptions from others (if found).   Cosmetic Information: None found   Suppliers: BOC Sciences For experimental / research use only. 2-Phenyl-2-pentenal Endeavour Specialty Chemicals 2-Phenyl-2-pentenal 90% F&F Speciality Chemical Product Groups R C Treatt & Co Ltd 2-Phenyl-2-pentenal Halal, Kosher Robinson Brothers 2-Phenyl-2-pentenal F&F https://www.robinsonbrothers.uk/chemistry-competences Santa Cruz Biotechnology For experimental / research use only. 2-Phenyl-2-pentenal, (E)+(Z) Sigma-Aldrich: Aldrich For experimental / research use only. 2-Phenyl-2-pentenal   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   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 2-phenyl-2-pentenal usage levels up to:   4.0000 % in the fragrance concentrate.   Maximised Survey-derived Daily Intakes (MSDI-EU): 0.011 (μg/capita/day) Structure Class: II   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 216: alpha,beta-Unsaturated aldehydes from chemical subgroup 3.3 of FGE.19: 2-Phenyl-2-alkenals[1] View page or View pdf Scientific Opinion on Flavouring Group Evaluation 216, Revision 1 (FGE.216Rev1). Consideration of genotoxic potential for a,ß-unsaturated 2-Phenyl -2-Alkenals from Subgroup 3.3 of FGE.19 View page or View pdf EPI System: View AIDS Citations:Search Cancer Citations:Search Toxicology Citations:Search EPA ACToR:Toxicology Data EPA Substance Registry Services (SRS):Registry Laboratory Chemical Safety Summary :3083805 National Institute of Allergy and Infectious Diseases:Data WGK Germany:3 2-phenylpent-2-enal Chemidplus:0003491632   References:   2-phenylpent-2-enal NIST Chemistry WebBook: Search Inchi Canada Domestic Sub. List: 3491-63-2 Pubchem (cid): 3083805 Pubchem (sid): 135232127   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 Export Tariff Code: 2912.19.0000 VCF-Online: VCF Volatile Compounds in Food ChemSpider: View   Potential Blenders and core components note For Odor aldehydic muguet undecadienal FR animal para- cresyl isobutyrate FL/FR para- cresyl phenyl acetate FL/FR balsamic cinnamyl alcohol FL/FR cinnamyl formate FL/FR 3- phenyl propyl alcohol FL/FR 2- phenyl propyl alcohol FL/FR chemical styralyl alcohol FL/FR citrus bergamot oil turkey FL/FR citronella oil java FR grapefruit pentanol FR fatty 2- decenal FL/FR fermented hexanal diethyl acetal FL/FR floral amyl benzoate FL/FR iso amyl salicylate FL/FR benzaldehyde propylene glycol acetal FL/FR alpha- butyl cinnamaldehyde FL/FR citronellal FL/FR (S)- citronellyl acetate FL/FR citronellyl acetate FL/FR citronellyl butyrate FL/FR citronellyl propionate FL/FR para- cresyl acetate FL/FR cumin carbinol FR cyclohexyl ethyl acetate FL/FR dihydrojasmone FL/FR dimethyl benzyl carbinol FL/FR dimethyl benzyl carbinyl acetate FL/FR dimethyl benzyl carbinyl butyrate FL/FR 6,8- dimethyl-2-nonanol FR ethyl hydrocinnamate FL/FR floral butanal FR gardenia concrete FR geranium oil bourbon FL/FR geranyl acetate FL/FR geranyl acetone FL/FR geranyl formate FL/FR geranyl hexanoate FL/FR geranyl isobutyrate FL/FR (Z)-3- hexen-1-yl salicylate FL/FR alpha- hexyl cinnamaldehyde FL/FR hyacinth ether FR hydroxycitronellal FL/FR hydroxycitronellol FL/FR beta- ionone FL/FR jasmin cyclopentanol FR jonquil absolute FR kewda oil CS lilac pentanol FL/FR lily flower absolute FR linalool oxide FL/FR magnolia indene FR para- methyl benzyl acetate FL/FR 4- methyl-4-phenyl-2-pentanol FR mimosa absolute france FL/FR mimosa absolute morocco FL/FR narcissus acetate FL/FR neroli oil bigarde FL/FR neroli oil CO2 extract FL/FR (E)- nerolidol FL/FR nerolidol FL/FR orange leaf absolute FL/FR papaya isobutyrate FL/FR phenethyl benzoate FL/FR phenethyl butyrate FL/FR phenethyl formate FL/FR phenethyl phenyl acetate FL/FR phenethyl salicylate FL/FR phenyl acetaldehyde / methyl anthranilate schiff's base FR phenyl glycol diacetate FR (S)-2- phenyl propionaldehyde FL/FR 2- phenyl propionaldehyde dimethyl acetal FL/FR 2- phenyl propionaldehyde ethylene glycol acetal FR 2- phenyl propyl acetate FL/FR (R)-2- phenyl propyl alcohol FL/FR 3- phenyl propyl formate FL/FR phenyl propyl phenyl acetate FR 3- phenyl propyl propionate FL/FR (E)-2- phenyl-1(2)-propene-1-yl acetate FR reseda acetal FR rose butanoate FL/FR sweet pea absolute FR tea acetate FR verdyl acetate FR wallflower absolute FR fruity benzyl methyl ether FL/FR decen-1-yl cyclopentanone FL/FR ethyl methyl-para-tolyl glycidate FL/FR furfuryl acetate FL/FR geranyl butyrate FL/FR prenyl acetate FL/FR green acetaldehyde ethyl phenethyl acetal FL/FR bromstyrol CS citrus carbaldehyde / methyl anthranilate schiff's base FR galbascone (IFF) FR green dioxolane FR green ether FL/FR heptyl cinnamate FL/FR (Z)-3- hexen-1-yl benzoate FL/FR (Z)-3- hexen-1-yl phenyl acetate FL/FR (Z)-3- hexen-1-yl tiglate FL/FR hyacinth absolute FL/FR hyacinth butanal FR 2,4- ivy carbaldehyde / methyl anthranilate schiff's base FR ivy dioxolane FR leafy acetal FL/FR marigold pot absolute FL/FR para- methyl hydratropaldehyde FL/FR methyl octine carbonate FL/FR octanal dimethyl acetal FL/FR 1- penten-3-ol FL/FR phenethyl oxyacetaldehyde FR phenoxyacetaldehyde 50% in benzyl alcohol FR phenyl acetaldehyde FL/FR phenyl acetaldehyde diethyl acetal FL/FR phenyl acetaldehyde ethylene glycol acetal FR phenyl acetaldehyde solution FL/FR 2- phenyl propionaldehyde FL/FR herbal dihexyl (E)-fumarate FR linalyl acetate FL/FR methyl ortho-anisate FL/FR rosmarinus officinalis extract FL/FR nutty 2,4,5- trimethyl oxazole FL/FR phenolic para- cresol FL/FR powdery para- anisyl alcohol FL/FR spicy alpha- amyl cinnamyl alcohol FL/FR sulfurous dimethyl sulfide FL/FR 2- methyl 5-(methyl thio) furan FL/FR 2- phenethyl isothiocyanate FL/FR waxy 3- decanone FL/FR orris rhizome oil CO2 extract FL/FR For Flavor No flavor group found for these amyl benzoate FL/FR 3- decanone FL/FR ethyl hydrocinnamate FL/FR heptyl cinnamate FL/FR hexanal diethyl acetal FL/FR hyacinth absolute FL/FR methyl ortho-anisate FL/FR 4- methyl thiobutyl isothiocyanate FL 6- methyl thiohexyl isothiocyanate FL 5- methyl thiopentyl isothiocyanate FL 4- pentenyl isothiocyanate FL 2- phenethyl isothiocyanate FL/FR phenyl acetaldehyde diethyl acetal FL/FR phenyl acetaldehyde solution FL/FR (S)-2- phenyl propionaldehyde FL/FR 2- phenyl propyl acetate FL/FR (R)-2- phenyl propyl alcohol FL/FR 3- phenyl propyl formate FL/FR 3- phenyl propyl propionate FL/FR alpha- butyl cinnamaldehyde FL/FR alliaceous alliaceous benzyl mercaptan FL cyclopentyl mercaptan FL 3- mercapto-2-pentanone FL aromatic para- cresyl acetate FL/FR para- cresyl isobutyrate FL/FR leafy acetal FL/FR burnt methyl phenyl disulfide FL 2,4,5- trimethyl oxazole FL/FR chemical styralyl alcohol FL/FR citrus bergamot oil turkey FL/FR estery furfuryl acetate FL/FR fatty 2- decenal FL/FR (Z)-3- hexen-1-yl benzoate FL/FR floral 2- acetyl-5-methyl thiophene FL citronellal FL/FR citronellyl acetate FL/FR (S)- citronellyl acetate FL/FR citronellyl propionate FL/FR dihydrojasmone FL/FR dimethyl benzyl carbinyl acetate FL/FR dimethyl benzyl carbinyl butyrate FL/FR geranium oil bourbon FL/FR geranyl acetone FL/FR geranyl isobutyrate FL/FR linalyl acetate FL/FR mimosa absolute morocco FL/FR neroli oil bigarde FL/FR neroli oil CO2 extract FL/FR orange leaf absolute FL/FR phenethyl benzoate FL/FR fruity para- anisyl alcohol FL/FR benzaldehyde propylene glycol acetal FL/FR benzyl methyl ether FL/FR citronellyl butyrate FL/FR decen-1-yl cyclopentanone FL/FR ethyl methyl-para-tolyl glycidate FL/FR geranyl butyrate FL/FR geranyl hexanoate FL/FR lilac pentanol FL/FR para- methyl benzyl acetate FL/FR phenethyl butyrate FL/FR 2- phenyl propionaldehyde dimethyl acetal FL/FR prenyl acetate FL/FR rose butanoate FL/FR green acetaldehyde ethyl phenethyl acetal FL/FR iso amyl salicylate FL/FR cinnamyl alcohol FL/FR cyclohexyl ethyl acetate FL/FR 2- furyl acetone FL geranyl acetate FL/FR geranyl formate FL/FR green ether FL/FR (Z)-3- hexen-1-yl phenyl acetate FL/FR (Z)-3- hexen-1-yl salicylate FL/FR (Z)-3- hexen-1-yl tiglate FL/FR hibiscus distillates FL linalool oxide FL/FR marigold pot absolute FL/FR para- methyl hydratropaldehyde FL/FR methyl octine carbonate FL/FR narcissus acetate FL/FR nerolidol FL/FR (E)- nerolidol FL/FR octanal dimethyl acetal FL/FR papaya isobutyrate FL/FR 1- penten-3-ol FL/FR phenethyl formate FL/FR 2- phenyl propionaldehyde FL/FR 2- phenyl propyl alcohol FL/FR herbal rosmarinus officinalis extract FL/FR honey phenethyl phenyl acetate FL/FR phenyl acetaldehyde FL/FR medicinal dimethyl benzyl carbinol FL/FR phenethyl salicylate FL/FR musty 2- methyl 5-(methyl thio) furan FL/FR onion methyl propyl disulfide FL phenolic para- cresol FL/FR para- cresyl phenyl acetate FL/FR powdery hydroxycitronellol FL/FR spicy alpha- amyl cinnamyl alcohol FL/FR benzyl isothiocyanate FL cinnamyl formate FL/FR 3- phenyl propyl alcohol FL/FR sulfurous allyl sulfide FL dimethyl sulfide FL/FR furfuryl methyl sulfide FL vegetable radish isothiocyanate FL waxy alpha- hexyl cinnamaldehyde FL/FR hydroxycitronellal FL/FR mimosa absolute france FL/FR woody beta- ionone FL/FR orris rhizome oil CO2 extract FL/FR   Potential Uses: FR bluebell FR clematis FR daffodil FR greenhouse FL horseradish FR hyacinth FR hydrangea FR jonquil FR kewda FR lotus FR narcissus FR privet blossom FL radish FL sesame FR wallflower   Occurrence (nature, food, other):note   sesame seed roasted Search Trop Picture   Synonyms:   benzeneacetaldehyde, a-propylidene- 2- phenyl pent-2-enal 2- phenyl-2-penten-1-al 2- phenylpent-2-enal alpha- propylidene benzene acetaldehyde   Articles:   None found yet. Try the PubMed Search.

Notes: None found