Il est constitué d'un cycle de benzène substitué par un groupe carboxyle, un groupe hydroxyle et un groupe méthoxyle en poitions 1, 3 et 4, ce qui fait de lui un vanilloïde. All rights reserved. Data Program, but require an annual fee to access. Enter the desired X axis range Standard Reference Data Act. Follow the links above to find out more about the data been selected on the basis of sound scientific judgment. with the development of data collections included in click the mouse on the plot to revert to the orginal display. Database and to verify that the data contained therein have Synonyms: Vanillic acid, isobutyl ester. View image of digitized Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file The 3d structure may be viewed using Java or Javascript. on behalf of the United States of America. and Informatics, NIST / TRC Web Thermo Tables, professional edition (thermophysical and thermochemical data), NIST Mass Spectrometry Data Center, William E. Wallace, director, Modified by NIST for use in this application. However, NIST makes no warranties to that effect, and NIST 1.) Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director. Data from NIST Standard Reference Database 69: The National Institute of Standards and Technology (NIST) and HTML 5 enabled browser. During cultivation, phenolic compounds such as syringic acid and vanillic acid are produced by lignin-degrading peroxidase secreted from L… Vanillic acid (4-hydroxy-3-methoxybenzoic acid) is a dihydroxybenzoic acid derivative used as a flavoring agent. uses its best efforts to deliver a high quality copy of the by the U.S. Secretary of Commerce on behalf of the U.S.A. Use or mention of technologies or programs in this web site is not It has a role as a plant metabolite. jcamp-plot.js. In addition, six minor degradation products were also found and identified as vanillin, vanillic acid (VA), ferulic aldehyde, FA, and 4-vinylguaiacol. Technology, Office of Data SCHEMBL5691342. C'est une forme oxydée de la vanilline (4-hydroxy-3-méthoxybenzaldéhy… It is an oxidized form of vanillin. its accompanying search program. in these sites and their terms of usage. The edible mushroom Lentinus edodes (shiitake) can be cultured in a solid medium, and its extract is commercially available as a nutritional supplement. The following components were used in generating the plot: Additonal code used was developed at NIST: jcamp-dx.js and DTXSID90221762. that these items are necessarily the best available for the purpose. the Methyl 4-hydroxy-3-methoxybenzoate, also known as vanillic acid or vanillATE, belongs to the class of organic compounds known as m-methoxybenzoic acids and derivatives.These are benzoic acids in which the hydrogen atom at position 3 of the benzene ring is replaced by a methoxy group. NIST Standard Reference HTML 5 canvas support. All rights reserved. errors or omissions in the Database. such sites. It is a conjugate acid of … It is a monohydroxybenzoic acid and a methoxybenzoic acid. CTK2H8791. L'acide vanillique ou acide 4-hydroxy-3-méthoxybenzoïque est un composé aromatique de formule C8H8O4, appartenant à la famille des acides-phénols, plus précisément des acides hydroxybenzoïques. 2004-09-16. Notice: This spectrum may be better viewed with a Javascript Molecular Formula: C12H16O4. intended to imply recommendation or endorsement by the National Institute of Standards and Technology, nor is it intended to imply Vanillic acid is a monohydroxybenzoic acid that is 4-hydroxybenzoic acid substituted by a methoxy group at position 3. Please see the following for information about Select a region with data to zoom. spectrum (can be printed in landscape orientation). Vanillic acid. available from the NIST/EPA/NIH Mass Spectral Library. © 2018 by the U.S. Secretary of Commerce NIST subscription sites provide data under the Molecular Formula C 8 H 8 O 4; Average mass 168.147 Da; Monoisotopic mass 168.042252 Da; ChemSpider ID 8155 shall not be liable for any damage that may result from Data compilation copyright Go To: Top, Mass spectrum (electron ionization), Notes, Go To: Top, Mass spectrum (electron ionization), References. The sixth degradation product could not be identified with available references, but had the empirical formula of C13 H 8 O 4. It is also an intermediate in the production of vanillin from ferulic acid. The purpose of the fee is to recover costs associated Copyright for NIST Standard Reference Data is governed by Create. All mass spectra in this site (plus many more) are 7152-88-7. The interactive spectrum display requires a browser with JavaScript and the library and (e.g., Japan AIST/NIMC Database- Spectrum MS-NW-2148. A chemical structure of a molecule includes the arrangement of atoms and the chemical bonds that hold the atoms together. Your institution may already be a subscriber. InChI=1S/C8H8O4/c1-12-7-4-5(8(10)11)2-3-6(7)9/h2-4,9H,1H3,(H,10,11), National Institute of Standards and Select a region with no data or