Qufu Shifan Daxue Xuebao, Ziran Kexueban (2005), 31(2), 96-98. Cinnamaldehyde is the aldehyde that gives cinnamon its flavor and odor. I’m 100% sure that a few years ago cinnamaldehyde oxime would be a perfect IUPAC name (Rule C-842.1), but currently, it will depend on the interpretation of the guidance. splash10-0059-3900000000-52db83b595237437ab08, splash10-0f89-5900000000-540c43f6893b35e8a105, splash10-0f89-5900000000-482f8b5c30c53689d8eb, splash10-001i-3900000000-9d274f5e3981ab662650, splash10-001i-0900000000-4f0ad7748ac21b7320c9, splash10-0f89-6900000000-ecaba4b9d657020c3f4c, splash10-001i-0900000000-c02b7869dea8f1113cb4, splash10-001i-2900000000-d89aa99ef7a6ae16b942, splash10-0ugi-8900000000-14f14e29c81360ebdd4b, Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive, splash10-0f89-4900000000-e9eb0053986096f21c83, LC-MS/MS Spectrum - Quattro_QQQ 10V, Positive (Annotated), splash10-0a59-5900000000-a125425df0f09bb01129, LC-MS/MS Spectrum - Quattro_QQQ 25V, Positive (Annotated), splash10-056r-9300000000-043ea317ed08a1cbacfb, LC-MS/MS Spectrum - Quattro_QQQ 40V, Positive (Annotated), splash10-004i-9000000000-39ab07ef5d737e851671, LC-MS/MS Spectrum - EI-B (HITACHI RMU-7M) , Positive, splash10-0f89-5900000000-f27dd11a8900d729bd19, LC-MS/MS Spectrum - EI-B (JEOL JMS-D-3000) , Positive, splash10-0f89-5900000000-4e11cf955911f9ca7da2, LC-MS/MS Spectrum - EI-B (SHIMADZU QP-1000) , Positive, LC-MS/MS Spectrum - EI-B (HITACHI RMU-6M) , Positive, splash10-0f89-6900000000-e363e674a4ec6e092f26, LC-MS/MS Spectrum - CI-B (HITACHI M-80) , Positive, splash10-001i-2900000000-7339e3ff66ab63ba3409, LC-MS/MS Spectrum - EI-B (HITACHI M-80B) , Positive, splash10-0ugi-8900000000-1b72d0d216af15365444, LC-MS/MS Spectrum - LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) , Positive, splash10-067i-2900000000-76d2db81f3822a698f0a, LC-MS/MS Spectrum - LC-ESI-QTOF , positive, Predicted LC-MS/MS Spectrum - 10V, Positive, splash10-001i-1900000000-4b1b083c8fdb2a27206b, Predicted LC-MS/MS Spectrum - 20V, Positive, splash10-00lr-2900000000-eee6045375789bd7b511, Predicted LC-MS/MS Spectrum - 40V, Positive, splash10-0f6x-9400000000-ffef407879854d06bd7e, Predicted LC-MS/MS Spectrum - 10V, Negative, splash10-001i-0900000000-074611feed644fd89c07, Predicted LC-MS/MS Spectrum - 20V, Negative, splash10-001i-0900000000-cbf5bec188b738c514af, Predicted LC-MS/MS Spectrum - 40V, Negative, splash10-01p6-9600000000-5eb930cf87b199a5f449. Cinnamaldehyde. This website uses cookies to ensure you get the best experience on our websites. [, Smith CK, Cheung C, Elahi EN, Hotchkiss SA: High-performance liquid chromatography method for the quantification of non-radiolabelled cinnamic compounds in analytes derived from human skin absorption and metabolism experiments. The Automated Topology Builder (ATB) and Repository is intended to facilitate the development of molecular force fields for Molecular Dynamics or Monte Carlo simulations of biomolecular systems. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). The content is subject to change without prior notice.Reproduction or further distribution of this information may be subject to copyright protection. These are organic aromatic compounds containing a cinnamlaldehyde moiety, consisting of a benzene and an aldehyde group to form 3-phenylprop-2-enal. 2000 Nov 1;168(3):189-99. Benvenuti al sito dell'ECHA. J Chromatogr B Biomed Sci Appl. [, Bandell M, Story GM, Hwang SW, Viswanath V, Eid SR, Petrus MJ, Earley TJ, Patapoutian A: Noxious cold ion channel TRPA1 is activated by pungent compounds and bradykinin. Aggiornare Internet Explorer a una versione più recente. J Am Acad Dermatol. The 2D chemical structure image of cinnamaldehyde is also called skeletal formula, which is the standard notation for organic molecules. Neuron. Please upgrade your Internet Explorer to a newer version. Cinnamaldehyde occurs naturally in the bark of cinnamon trees and other species of the genus Cinnamomum like camphor and cassia. Dtsch Z Verdau Stoffwechselkr. belongs to the class of organic compounds known as cinnamaldehydes. Quantitative metabolomics services for biomarker discovery and validation. Display Name: Cinnamaldehyde EC Number: 203-213-9 EC Name: Cinnamaldehyde CAS Number: 104-55-2 Molecular formula: C9H8O IUPAC Name: (2E)-3-phenylprop-2-enal This information has not been reviewed or verified by the Agency or any other authority. 2003 Feb;48(2):194-200. Cinnamaldehyde is an organic compound with the formula C 6 H 5 CH=CHCHO. Applications include the study of biomolecule:ligand complexes, free energy calculations, structure-based drug design and refinement of x-ray crystal complexes. Welcome to the ECHA website. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). Cinnamaldehyde occurs naturally in the bark of cinnamon trees and other species of the genus Cinnamomum like camphor and cassia. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner. EC number: 203-213-9 | CAS number: 104-55-2 . Occurring naturally as predominantly the trans isomer, it gives cinnamon its flavor and odor. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner. The content is subject to change without prior notice.Reproduction or further distribution of this information may be subject to copyright protection. [, Bruze M, Johansen JD, Andersen KE, Frosch P, Lepoittevin JP, Rastogi S, Wakelin S, White I, Menne T: Deodorants: an experimental provocation study with cinnamic aldehyde. This site is not fully supported in Internet Explorer 7 (and earlier versions). Its low toxicity and well-known properties make it ideal for agriculture. InChI=1S/C9H8O/c10-8-4-7-9-5-2-1-3-6-9/h1-8H/b7-4+, The Metabolomics Innovation Centre (TMIC). Close Find out more on how we use cookies. The carbon atoms in the chemical structure of cinnamaldehyde are implied to be located at the corner(s) and hydrogen atoms attached to carbon atoms are not indicated – each carbon atom is considered to be associated with enough hydrogen atoms to provide … Most cinnamaldehyde is excreted in urine as cinnamic acid, an oxidized form of cinnamaldehyde. Muller G, Biering A, Graubaum K, Jeschkeit H, Neubert K, Kleine R, Klapperstuck M: [The PABA test]. Toxicol Appl Pharmacol. General information; ... EC name: 2-phenylethanol CAS number: 60-12-8 No inventory information available Reference substance information IUPAC name: 2-phenylethan-1-ol CAS information CAS number: 60-12-8 Molecular and structural information Molecular formula: C8H10O Chiuso Non mostrare più questo messaggio. Synthesis of cinnamaldehyde. EC number: 203-213-9 | CAS number: 104-55-2. Information on Registered Substances comes from registration dossiers which have been assigned a registration number. 2004 Mar 25;41(6):849-57. 2001 Jul 15;758(2):249-64. Chiuso Per saperne di più su come utilizziamo i cookie. Learn more about cinnamaldehyde chemical formula at Mol-Instincts. Proven effective on over 40 different crops, cinnamaldehyde is typically applied to the root systems of plants. Liu, Xue-mei. Particle size distribution (Granulometry), Solubility in organic solvents / fat solubility, Stability in organic solvents and identity of relevant degradation products, Storage stability and reactivity towards container material, Biodegradation in water and sediment: simulation tests, Additional information on environmental fate and behaviour, Short-term toxicity to aquatic invertebrates, Long-term toxicity to aquatic invertebrates, Toxicity to aquatic algae and cyanobacteria, Toxicity to aquatic plants other than algae, Endocrine disrupter testing in aquatic vertebrates – in vivo, Toxicity to soil macroorganisms except arthropods, Endocrine disrupter mammalian screening – in vivo (level 3), Direct observations: clinical cases, poisoning incidents and other, Exposure related observations in humans: other data, Additional physico-chemical properties of nanomaterials, Toxicokinetics, metabolism and distribution. Information on Registered Substances comes from registration dossiers which have been assigned a registration number. Common Name: Cinnamaldehyde: Description: Cinnamaldehyde is the aldehyde that gives cinnamon its flavor and odor. It can be used in combination with additional components such as dispersing agents, solvents and other surfactants. Concentrated cinnamaldehyde is a skin irritant, and the chemical is toxic in large doses, but no agencies suspect the compound is a carcinogen or poses a long-term health hazard. Your source for quantitative metabolomics technologies and bioinformatics. Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice. Cinnamaldehyde is also used as a fungicide. This information has not been reviewed or verified by the Agency or any other authority. [. Specializing in ready to use metabolomics kits. Cinnamaldehyde is also known as a corrosion inhibitor for steel and other ferrous alloys in corrosive fluids. These trees are the natural source of cinnamon, and the essential oil of cinnamon bark is about 90% cinnamaldehyde. Questo sito web si avvale di cookie affinché possiate usufruire della migliore esperienza sui nostri siti web. EC number: 203-213-9 | CAS number: 104-55-2. [, Smith CK, Moore CA, Elahi EN, Smart AT, Hotchkiss SA: Human skin absorption and metabolism of the contact allergens, cinnamic aldehyde, and cinnamic alcohol. Particle size distribution (Granulometry), Solubility in organic solvents / fat solubility, Stability in organic solvents and identity of relevant degradation products, Storage stability and reactivity towards container material, Biodegradation in water and sediment: simulation tests, Additional information on environmental fate and behaviour, Short-term toxicity to aquatic invertebrates, Long-term toxicity to aquatic invertebrates, Toxicity to aquatic algae and cyanobacteria, Toxicity to aquatic plants other than algae, Endocrine disrupter testing in aquatic vertebrates – in vivo, Toxicity to soil macroorganisms except arthropods, Endocrine disrupter mammalian screening – in vivo (level 3), Direct observations: clinical cases, poisoning incidents and other, Exposure related observations in humans: other data, Additional physico-chemical properties of nanomaterials, Toxicokinetics, metabolism and distribution. It is a phenylpropanoid that is naturally synthesized by the shikimate pathway. 1984;44(5):219-31. Structure, properties, spectra, suppliers and links for: (Z)-cinnamaldehyde. Cinnamaldehyde contains total 18 atom(s); 8 Hydrogen atom(s), 9 Carbon atom(s) and 1 Oxygen atom(s). Non tutte le funzionalità del presente sito sono fruibili con Internet Explorer 7 (e versioni precedenti). Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice. To a lesser extent, cinnamaldehyde is an effective insecticide, and its scent is also known to repel animals like cats and dogs.