Cinnamaldehyde is also known as a corrosion inhibitor for steel and other ferrous alloys in corrosive fluids. Common Name: Cinnamaldehyde: Description: Cinnamaldehyde is the aldehyde that gives cinnamon its flavor and odor. 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. [, 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. Chiuso Per saperne di più su come utilizziamo i cookie. This information has not been reviewed or verified by the Agency or any other authority. Cinnamaldehyde occurs naturally in the bark of cinnamon trees and other species of the genus Cinnamomum like camphor and cassia. Structure, properties, spectra, suppliers and links for: (Z)-cinnamaldehyde. Cinnamaldehyde. Aggiornare Internet Explorer a una versione più recente. It can be used in combination with additional components such as dispersing agents, solvents and other surfactants. Non tutte le funzionalità del presente sito sono fruibili con Internet Explorer 7 (e versioni precedenti). Cinnamaldehyde contains total 18 atom(s); 8 Hydrogen atom(s), 9 Carbon atom(s) and 1 Oxygen atom(s). Proven effective on over 40 different crops, cinnamaldehyde is typically applied to the root systems of plants. Applications include the study of biomolecule:ligand complexes, free energy calculations, structure-based drug design and refinement of x-ray crystal complexes. Cinnamaldehyde is also used as a fungicide. [, Smith CK, Moore CA, Elahi EN, Smart AT, Hotchkiss SA: Human skin absorption and metabolism of the contact allergens, cinnamic aldehyde, and cinnamic alcohol. Quantitative metabolomics services for biomarker discovery and validation. 2001 Jul 15;758(2):249-64. Muller G, Biering A, Graubaum K, Jeschkeit H, Neubert K, Kleine R, Klapperstuck M: [The PABA test]. Neuron. 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. Close Find out more on how we use cookies. 2000 Nov 1;168(3):189-99. 2004 Mar 25;41(6):849-57. This information has not been reviewed or verified by the Agency or any other authority. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner. Occurring naturally as predominantly the trans isomer, it gives cinnamon its flavor and odor. 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. The 2D chemical structure image of cinnamaldehyde is also called skeletal formula, which is the standard notation for organic molecules. Toxicol Appl Pharmacol. Learn more about cinnamaldehyde chemical formula at Mol-Instincts. It is a phenylpropanoid that is naturally synthesized by the shikimate pathway. The content is subject to change without prior notice.Reproduction or further distribution of this information may be subject to copyright protection. This site is not fully supported in Internet Explorer 7 (and earlier versions). Your source for quantitative metabolomics technologies and bioinformatics. Chiuso Non mostrare più questo messaggio. J Am Acad Dermatol. Benvenuti al sito dell'ECHA. 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. Specializing in ready to use metabolomics kits. Cinnamaldehyde is the aldehyde that gives cinnamon its flavor and odor. Information on Registered Substances comes from registration dossiers which have been assigned a registration number. 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 … Qufu Shifan Daxue Xuebao, Ziran Kexueban (2005), 31(2), 96-98. Cinnamaldehyde is an organic compound with the formula C 6 H 5 CH=CHCHO. 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). Most cinnamaldehyde is excreted in urine as cinnamic acid, an oxidized form of cinnamaldehyde. Synthesis of cinnamaldehyde. EC number: 203-213-9 | CAS number: 104-55-2. 2003 Feb;48(2):194-200. Please upgrade your Internet Explorer to a newer version. Its low toxicity and well-known properties make it ideal for agriculture. Dtsch Z Verdau Stoffwechselkr. Welcome to the ECHA website. 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. belongs to the class of organic compounds known as cinnamaldehydes. 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. EC number: 203-213-9 | CAS number: 104-55-2 . Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner. 1984;44(5):219-31. [, 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. 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. 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.