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vanillic acid found in

Other in vivo and in vitro studies have confirmed the ability of PCA in counteracting NO production. 2015 Jan;39(1):1-6. doi: 10.1016/j.jgr.2014.10.006. The main identified degradation product had the chemical composition of C12H18O6, with a mass spectrum exhibiting a molecular ion at m/e = 366 (indicating that two hydrogen atoms were removed from its structure). BOD5/COD ratio provides substance information on the substance’s BOD5/COD ratio values displayed in O2 (milli)gram per gram test material. COD provides substance information on the substance’s COD values displayed in O2 (milli)gram per gram test material. Solubility in mg/100g standard fat at 20°C provides substance information on the substance solubility in standard fat in milligram per 100 gram at a temperature of 20°C. For accuracy reasons, substance manufacturers and importers are responsible for consulting official sources. This section provides environmental fate and pathways information compiled from all automatically processable data from REACH registration dossiers that is available to ECHA at the time of generation. pKa at 20°C provides numerical substance information on the dissociation constant in pKa at a temperature of 20°C. Half-life for hydrolysis provides substance information on the substance’s half-life for hydrolysis in seconds/minutes/hours/days/weeks/months/years at a temperature measured in °C.Note: Results without a measurement condition (temperature) are not processed for the Brief Profile. Thirdly the display of data is prioritised by units. Significant synergism was found in the majority of the all combinations, as well as the combination of the four phenolics. Meldung für das Einstufungs- und Kennzeichnungsverzeichnis. The Index number for each substance is in the form of a digit sequence of the type ABC-RST-VW-Y. By continuing you agree to the use of cookies. This section provides physicochemical information compiled from all automatically processable data from REACH registration dossiers that is available to ECHA at the time of generation. Honey is also recognized for its in vivo antioxidant effect which has been documented in body fluids (plasma), cells (red blood cells), tissues, and organs such as liver, pancreas, kidney, and eye. Hazard statements were adapted to improve readability and may not correspond textually to the hazard statements codes description in the European Union Specific Hazard Statements (EUH) or the. Values are generally displayed in milligram per litre. For example, substance impurities can constitute a valid reason for a different classification of the substance. EC10 / LC10 or NOEC for microorganisms provides substance information on the substance’s effect concentration/lethal concentration for 10% of the tested microorganisms or the no observed effect concentration for microorganisms. Processable data for summary is prioritised by test species (see list below) and subsequently further prioritised by the dose descriptor. This section summarises the Ecotoxicological information provided from all registered dossiers for the substance. More detailed description of antioxidant features and properties of honey as well as its effects on oxidative stress parameters in different tissues and organs is already reviewed by Erejuwa et al.62. The results of matching substance classifications are displayed in percentages of the total number of notifications. Registrants can identify the origin of their substance as being: If more than one type of substance is registered, both types will be displayed. Pre-registration allows companies to continue manufacturing and importing their. This section summarises the values related to toxicity to aquatic algae and cyanobacteria from all registered dossiers for the substance. disodium tetraborate EC no. The recommendations are based on the precautionary statements provided in REACH registration dossiers. Vanillic acid is used in the synthesis of: InChI=1S/C8H8O4/c1-12-7-4-5(8(10)11)2-3-6(7)9/h2-4,9H,1H3,(H,10,11), InChI=1/C8H8O4/c1-12-7-4-5(8(10)11)2-3-6(7)9/h2-4,9H,1H3,(H,10,11), Except where otherwise noted, data are given for materials in their, Last edited on 23 September 2020, at 04:03, "Vanillic acid (4-hydroxy-3-methoxybenzoic acid)", "Bioconversion of ferulic acid into vanillic acid by means of a vanillate-negative mutant of Pseudomonas fluorescens strain BF13", https://en.wikipedia.org/w/index.php?title=Vanillic_acid&oldid=979848615, Creative Commons Attribution-ShareAlike License, 210 to 213 °C (410 to 415 °F; 483 to 486 K), Vanillic acid is acetylated and converted to its acid chloride; S.B.

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