Occurring naturally as predominantly the trans isomer, it gives cinnamon its flavor and odor. belongs to the class of organic compounds known as cinnamaldehydes. EC number: 203-213-9 | CAS number: 104-55-2. EC number: 203-213-9 | CAS number: 104-55-2 . Cinnamaldehyde is an organic compound with the formula C 6 H 5 CH=CHCHO. Common Name: Cinnamaldehyde: Description: Cinnamaldehyde is the aldehyde that gives cinnamon its flavor and odor. 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. 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 The content is subject to change without prior notice.Reproduction or further distribution of this information may be subject to copyright protection. Cinnamaldehyde. Muller G, Biering A, Graubaum K, Jeschkeit H, Neubert K, Kleine R, Klapperstuck M: [The PABA test].

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. Close Find out more on how we use cookies. 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. 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 … It is a phenylpropanoid that is naturally synthesized by the shikimate pathway. Chiuso Non mostrare più questo messaggio. Cinnamaldehyde contains total 18 atom(s); 8 Hydrogen atom(s), 9 Carbon atom(s) and 1 Oxygen atom(s). 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. 2000 Nov 1;168(3):189-99. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner. 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. Your source for quantitative metabolomics technologies and bioinformatics. [, 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. Structure, properties, spectra, suppliers and links for: (Z)-cinnamaldehyde.

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.

Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner. Welcome to the ECHA website. Synthesis of cinnamaldehyde. Cinnamaldehyde is also used as a fungicide. Qufu Shifan Daxue Xuebao, Ziran Kexueban (2005), 31(2), 96-98. Neuron. These are organic aromatic compounds containing a cinnamlaldehyde moiety, consisting of a benzene and an aldehyde group to form 3-phenylprop-2-enal. The content is subject to change without prior notice.Reproduction or further distribution of this information may be subject to copyright protection.

Applications include the study of biomolecule:ligand complexes, free energy calculations, structure-based drug design and refinement of x-ray crystal complexes. Cinnamaldehyde occurs naturally in the bark of cinnamon trees and other species of the genus Cinnamomum like camphor and cassia. These trees are the natural source of cinnamon, and the essential oil of cinnamon bark is about 90% cinnamaldehyde. 1984;44(5):219-31. [. Specializing in ready to use metabolomics kits. This information has not been reviewed or verified by the Agency or any other authority. 2003 Feb;48(2):194-200. J Chromatogr B Biomed Sci Appl. Learn more about cinnamaldehyde chemical formula at Mol-Instincts. Cinnamaldehyde is the aldehyde that gives cinnamon its flavor and odor.

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). Toxicol Appl Pharmacol. 2001 Jul 15;758(2):249-64. J Am Acad Dermatol.

It can be used in combination with additional components such as dispersing agents, solvents and other surfactants. Cinnamaldehyde is also known as a corrosion inhibitor for steel and other ferrous alloys in corrosive fluids. Information on Registered Substances comes from registration dossiers which have been assigned a registration number. Questo sito web si avvale di cookie affinché possiate usufruire della migliore esperienza sui nostri siti web. Benvenuti al sito dell'ECHA. EC number: 203-213-9 | CAS number: 104-55-2. 2004 Mar 25;41(6):849-57. To a lesser extent, cinnamaldehyde is an effective insecticide, and its scent is also known to repel animals like cats and dogs. 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.

This site is not fully supported in Internet Explorer 7 (and earlier versions). 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. Please upgrade your Internet Explorer to a newer version.

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