2000 Nov 1;168(3):189-99. Cinnamaldehyde occurs naturally in the bark of cinnamon trees and other species of the genus Cinnamomum like camphor and cassia. Toxicol Appl Pharmacol. 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.

1984;44(5):219-31. Muller G, Biering A, Graubaum K, Jeschkeit H, Neubert K, Kleine R, Klapperstuck M: [The PABA test]. [, 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 content is subject to change without prior notice.Reproduction or further distribution of this information may be subject to copyright protection. Synthesis of cinnamaldehyde. Neuron. belongs to the class of organic compounds known as cinnamaldehydes.

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. Learn more about cinnamaldehyde chemical formula at Mol-Instincts. Chiuso Non mostrare più questo messaggio.

Liu, Xue-mei. 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. Benvenuti al sito dell'ECHA. 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. EC number: 203-213-9 | CAS number: 104-55-2. Questo sito web si avvale di cookie affinché possiate usufruire della migliore esperienza sui nostri siti web.

J Chromatogr B Biomed Sci Appl. 2003 Feb;48(2):194-200. The 2D chemical structure image of cinnamaldehyde is also called skeletal formula, which is the standard notation for organic molecules. Please upgrade your Internet Explorer to a newer version. These trees are the natural source of cinnamon, and the essential oil of cinnamon bark is about 90% cinnamaldehyde. It is a phenylpropanoid that is naturally synthesized by the shikimate pathway. Occurring naturally as predominantly the trans isomer, it gives cinnamon its flavor and odor.

This website uses cookies to ensure you get the best experience on our websites. Information on Registered Substances comes from registration dossiers which have been assigned a registration number. J Am Acad Dermatol. This information has not been reviewed or verified by the Agency or any other authority. Cinnamaldehyde is the aldehyde that gives cinnamon its flavor and odor. 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. It can be used in combination with additional components such as dispersing agents, solvents and other surfactants. 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 … EC number: 203-213-9 | CAS number: 104-55-2 . Dtsch Z Verdau Stoffwechselkr. Chiuso Per saperne di più su come utilizziamo i cookie.

This site is not fully supported in Internet Explorer 7 (and earlier versions). [, 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. These are organic aromatic compounds containing a cinnamlaldehyde moiety, consisting of a benzene and an aldehyde group to form 3-phenylprop-2-enal. To a lesser extent, cinnamaldehyde is an effective insecticide, and its scent is also known to repel animals like cats and dogs.

Cinnamaldehyde is also used as a fungicide. Applications include the study of biomolecule:ligand complexes, free energy calculations, structure-based drug design and refinement of x-ray crystal complexes. Cinnamaldehyde is an organic compound with the formula C 6 H 5 CH=CHCHO. Its low toxicity and well-known properties make it ideal for agriculture. [, Smith CK, Moore CA, Elahi EN, Smart AT, Hotchkiss SA: Human skin absorption and metabolism of the contact allergens, cinnamic aldehyde, and cinnamic alcohol. [. This information has not been reviewed or verified by the Agency or any other authority. 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 2004 Mar 25;41(6):849-57. The content is subject to change without prior notice.Reproduction or further distribution of this information may be subject to copyright protection. Non tutte le funzionalità del presente sito sono fruibili con Internet Explorer 7 (e versioni precedenti). InChI=1S/C9H8O/c10-8-4-7-9-5-2-1-3-6-9/h1-8H/b7-4+, The Metabolomics Innovation Centre (TMIC). Aggiornare Internet Explorer a una versione più recente. Proven effective on over 40 different crops, cinnamaldehyde is typically applied to the root systems of plants. 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. 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.


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). Qufu Shifan Daxue Xuebao, Ziran Kexueban (2005), 31(2), 96-98. Specializing in ready to use metabolomics kits. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner. Your source for quantitative metabolomics technologies and bioinformatics. Information on Registered Substances comes from registration dossiers which have been assigned a registration number.

EC number: 203-213-9 | CAS number: 104-55-2.

Most cinnamaldehyde is excreted in urine as cinnamic acid, an oxidized form of cinnamaldehyde. 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.

Cinnamaldehyde occurs naturally in the bark of cinnamon trees and other species of the genus Cinnamomum like camphor and cassia. Cinnamaldehyde. Cinnamaldehyde is also known as a corrosion inhibitor for steel and other ferrous alloys in corrosive fluids. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.