Close Find out more on how we use cookies. InChI=1S/C9H8O/c10-8-4-7-9-5-2-1-3-6-9/h1-8H/b7-4+, The Metabolomics Innovation Centre (TMIC). The 2D chemical structure image of cinnamaldehyde is also called skeletal formula, which is the standard notation for organic molecules. Information on Registered Substances comes from registration dossiers which have been assigned a registration number. Applications include the study of biomolecule:ligand complexes, free energy calculations, structure-based drug design and refinement of x-ray crystal complexes. Its low toxicity and well-known properties make it ideal for agriculture.

2004 Mar 25;41(6):849-57. This website uses cookies to ensure you get the best experience on our websites.

Muller G, Biering A, Graubaum K, Jeschkeit H, Neubert K, Kleine R, Klapperstuck M: [The PABA test]. Cinnamaldehyde is also known as a corrosion inhibitor for steel and other ferrous alloys in corrosive fluids. Cinnamaldehyde contains total 18 atom(s); 8 Hydrogen atom(s), 9 Carbon atom(s) and 1 Oxygen atom(s). Cinnamaldehyde is the aldehyde that gives cinnamon its flavor and odor. 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.

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Common Name: Cinnamaldehyde: Description: Cinnamaldehyde is the aldehyde that gives cinnamon its flavor and odor. Learn more about cinnamaldehyde chemical formula at Mol-Instincts. Dtsch Z Verdau Stoffwechselkr. These are organic aromatic compounds containing a cinnamlaldehyde moiety, consisting of a benzene and an aldehyde group to form 3-phenylprop-2-enal. 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. Questo sito web si avvale di cookie affinché possiate usufruire della migliore esperienza sui nostri siti web. [, Smith CK, Moore CA, Elahi EN, Smart AT, Hotchkiss SA: Human skin absorption and metabolism of the contact allergens, cinnamic aldehyde, and cinnamic alcohol. Benvenuti al sito dell'ECHA. 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 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. 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. Qufu Shifan Daxue Xuebao, Ziran Kexueban (2005), 31(2), 96-98. EC number: 203-213-9 | CAS number: 104-55-2. 2000 Nov 1;168(3):189-99. Cinnamaldehyde is also used as a fungicide. This information has not been reviewed or verified by the Agency or any other authority. Structure, properties, spectra, suppliers and links for: (Z)-cinnamaldehyde. 1984;44(5):219-31. Cinnamaldehyde. It is a phenylpropanoid that is naturally synthesized by the shikimate pathway. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner. 2001 Jul 15;758(2):249-64. It can be used in combination with additional components such as dispersing agents, solvents and other surfactants. 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. Your source for quantitative metabolomics technologies and bioinformatics. J Chromatogr B Biomed Sci Appl. Cinnamaldehyde is an organic compound with the formula C 6 H 5 CH=CHCHO. Specializing in ready to use metabolomics kits. Non tutte le funzionalità del presente sito sono fruibili con Internet Explorer 7 (e versioni precedenti). 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). Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner. Aggiornare Internet Explorer a una versione più recente. Quantitative metabolomics services for biomarker discovery and validation. Information on Registered Substances comes from registration dossiers which have been assigned a registration number. Toxicol Appl Pharmacol. 2003 Feb;48(2):194-200. To a lesser extent, cinnamaldehyde is an effective insecticide, and its scent is also known to repel animals like cats and dogs. J Am Acad Dermatol.

Cinnamaldehyde occurs naturally in the bark of cinnamon trees and other species of the genus Cinnamomum like camphor and cassia. 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. 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 EC number: 203-213-9 | CAS number: 104-55-2 .

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