The mass spectrum of fractions 6 and 8 was represented in Figs 2 and 3. The MALDI-TOF spectrum showed a peak series exhibiting a mass increment of 288 Da, reflecting the variation in the number of catechin/epicatechin units. 3,4,5-Trihydroxybenzanilide. Gallic acid was isolated from EtOAc by another method previously reported by Ben Saad and Kim, 2015 . It is highly specific for gallic acid. 72 mass spectra in 1 spectral trees are available online for the compound Gallic acid . as eluent, toluene-acetone-formic acid (3:6:1), and the plates were developed with UV light (254 nm and 365 nm), vanillin, iron chloride and an iodine chamber to establish the composition of the fractions. The air-oxidation of gallic acid at near-neutral pH produces a semiquinone free radical that is easily observed by electron paramagnetic spectroscopy (EPR), Figure 1.This spectrum appears as a doublet of triplets and consistent with hyperfine splittings by three protons having hyperfine splitting constants of 1.00 G, 0.23 G, ⦠Obtention of ⦠Their fragmentation pattern and molecular weight of fractions 5 and 8 showed the presence of gallic acid and catechin in faba bean seed extract . This is consistent with three hydrogens providing hyperfine splitting. 6a). It is found both as a free state and as a constituent of tannins, namely, gallotannin. Based on the previous studies on its metabolic fate, gallic acid will be metabolized through decarboxylation, O-methylation, sulfation, and glucuronidation reactions in rats [18, 19]. Methods Serum samples incubated with gallic acid were subjected to LC/MS/MS analysis using an LTQ XL ion trap mass spectrometer. Helium was the carrier gas at constant flow of 0.7 ml/min. It is commonly used in the pharmaceutical industry. Gallic acid glycoside was enzymatically synthesized by using dextransucrase and sucrose from gallic acid. 2.4.1. The temperature of the mass spectrometer (MS) source, MS quadrupole, and the transfer line into the MS were 230, 150, and 280°C respectively. Gallic acid is a phenolic compound also known as 3,4,5-trihydroxybenzoic acid. 240 Natural Product Communications Vol. In the present work, gallic acid as a trapping agent of blood formaldehyde was investigated by liquid chromatography/tandem mass spectrometry (LC/MS/MS) and neutral loss scan. A similar fragment ion at m/z 111.0452 was observed by loss of gallic acid (GOH, ⦠Other names: Gallic acid; 3,4,5-Trihydroxybenzoic acid; Kyselina gallova; Kyselina 3,4,5-trihydroxybenzoova Permanent link for this species. GA have been reported to have potent free radical scavenging and anti-oxidative activities [10] , [11] and therefore the study of the mechanism of action of GA has received much ⦠Gallic acid (GA), an endogenous plant phenol, is a naturally abundant plant compound in vegetables, tea, grapes, berries, as well as wine â. The data also suggest CAS ⦠mzCloud â Free Online Mass Spectrometry Database View the Full Spectrum for FREE! ... Mass spectrum showing the presence of ellagic acid ⦠LC-MS Waters was used for mass detection. Gallic acid is a water soluble phenolic acid present in grapes and in the leaves of many plants. The exact position of this broad band depends on whether the carboxylic acid is saturated or unsaturated, dimerized, or has internal hydrogen bonding. 3,4,5-Trihydroxybenzoic acid monohydrate. The yield of gallic acid ⦠Gallic acid: Description: Gallic acid is an organic acid, also known as 3,4,5-trihydroxybenzoic acid, found in gallnuts, sumac, witch hazel, tea leaves, oak bark, and other plants. Oxygen-sensitive gallic acid decarboxylase from Pantoea (formerly Enterobacter ) agglomerans T71 was purified from a cell extract after stabilization by reducing agents. The fatty acid composition was identified by a mass spectrum database (NIST Library, mass spectral search program, version ⦠Gallicacidmonohydrate However, gallic acid itself also appears to have antioxidant, anticarcinogenic and antiangiogenic activity in vitro. Gallic acid esters, such as tannins, catechin gallates and aliphatic gallates are potent antioxidants in vitro. After introduction of gallic acid QCG (Fig. Phenolic compounds (delphinidin and gallic acid), at concentrations that encompassed the physiologically relevant range (10 nMâ100 μM), were prepared in tissue culture medium prior to addition of Tempone-H (10 mM stock, dissolved in ultrapure water) to generate a final concentration of 2 mM. 3,4,5-trihydroxybenzoic acid hydrate. Synonym: 3,5-Dimethoxy-4-hydroxybenzoic acid, 4-Hydroxy-3,5-dimethoxy-benzoic acid, Gallic acid 3,5-dimethyl ether Linear Formula: HOC 6 H 2 (OCH 3 ) 2 CO 2 H Molecular Weight: 198.17 The chemical formula is C6H2(OH)3CO2H. Figure 5: Mass spectra of (A) Catechin (Cf 1) and (B) Gallic acid (Cf 2). 11 (2) 2016 Singh et al. Mass spectra were recorded in negative and positive ionization modes with the ion source voltage of 4.95 kV, the source current of 2.61 μA, the capillary temperature of 275 °C, the capillary voltage of 50 V, the sheath gas pressure of 137 KPa and auxiliary gas pressure of 13.9 KPa. After 18 h treatment with Gallic acid, the number of viable neutrophils is dramatically decreased from 40.3% to 27.7%, highly comparable with 26.4% for untreated neutrophils. Ellagic acid, gallic acid and punicalagin A&B potentially inhibited LPS-induced NO, PGE-2 and IL-6 production. CAS=121-79-9, Molecular Formula=C 10 H 12 O 5, Molecular Weight (g/mol)=212.2, MDL Number=MFCD00002196, InChI Key=ZTHYODDOHIVTJV-UHFFFAOYSA-N, Synonym=propyl gallate,n-propyl gallate,progallin p,tenox pg,nipagallin p,gallic acid, propyl ester,gallic acid propyl ester,nipa 49,benzoic acid, 3,4,5-trihydroxy-, ⦠Salts and esters of gallic acid ⦠As the precursor of tannin, gallic acid presented an [M-H] â ion at m/z 169 in the full scan mass spectrum. Go To: Top, Mass spectrum (electron ionization), Gas Chromatography, References Data from NIST Standard Reference Database 69: NIST Chemistry WebBook The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein ⦠Gallic acid is found both free and as part of tannins. In our work, the gallic acid, which was produced by the hydrolysis of BG, proved to undergo further metabolic reactions including O-methylation and ⦠Our results suggest CAS contains polyphenols with strong α-amylase inhibitory activity. Spectrum analysis showed the same Rf values and spectrum pattern of standard and sample. This enzyme has a molecular mass of approximately 320 kDa and consists of six identical subunits. 4. 95 Gallic acid has been shown to effectively ⦠137.0244 was observed by loss of gallic acid (GOH, Îm=170) and water (H2O, Îm=18) molecules.Ion at m/z 137.0244 underwent CO2 loss to generate ion at m/z 93.0346. The molecular structure of gallic acid and catechin were predicted in Fig. Gallic acid chloride was synthesized by the dropwise addition, over a period of 0.25hr, of 3.16ml (44.3mmol) of thionyl chloride to a solu-tion of 5.03g (29.6mmol) of gallic acid and three drops of dimethylformamide in 20ml of anhydrous tetrahydrofuran (THF) maintained near ⦠Gallic acid, catechin and cinnamic acid and related derivatives originated form rhubarb. Gallic acid and its derivatives are present in nearly every part of the plant, such as bark, wood, leaf, fruit, root, and seed. Gallic acid decarboxylase ⦠Gallic acid monohydrate. As an ACS grade quality reagent, its chemical specifications are the de facto standards for chemicals used in many high-purity ⦠Results. We found that gallic acid produces two different radicals as a function of pH. In TLC, standards of catechin and Gallic acid were also used (gallic acid, Rf 0.88; catechin, Rf 0.86) [27]. Use this link for bookmarking this species for future reference. The resulting spectrum showed the presence of three initiator species, at m/z ratios of 498, 514, and 530, formed by a reaction between tertiary amine and epoxides precursors, i.e., di-, tri-, and tetra-glycidyl ether of gallic acid, respectively (Fig. In the pH range between 7-10, the spectrum of the gallate free radical is a doublet of triplets (a H = 1.00 G, a H = 0.23 G, a H = 0.28 G). Cell culture. OâH stretch from 3300-2500 cm-1; C=O stretch from 1760-1690 cm-1; CâO stretch from 1320-1210 cm-1; OâH bend from 1440-1395 and 950-910 cm-1; Figure 11. shows the spectrum of hexanoic acid ⦠1B) has a peak of symmetric protons in the 1 H NMR spectrum the formation of a new amide and ester bonds in the IR spectrum is seen in the region of 1550â1700 cm â1. Gallic Acid, Monohydrate, Crystal, Reagent, ACS, also known as 3,4,5-trihydroxybenzoic acid, can be used as a starting material in the synthesis of the psychedelic alkaloid mescaline. Information on this page: Mass spectrum (electron ionization) References; Notes; Other data available: ⦠In addition to quercetin, the presence of gallic acid, Liquid chromatographyâelectrospray ionization tandem mass spectrometry has been used for rapid, selective, and sensitive quantitative analysis of gallic acid ⦠The developed method was quite good and most ⦠After purification by butanol partitioning and preparative HPLC, gallic acid glucoside was detected at m/z 355 (C13, H16, O10, Na)+ by matrix-assisted laser desorption ionization time-of-flight mass spectrometry. The fragment of the [M-H-CO 2 ] â ion at m/z 125 was shown in the MSâMS experiment. μg mL-1 for ascorbic acid and 5â15 μg mL for gallic acid, respectively. Gallic acid fails to attenuate isoproterenol-induced myocytolysis[3]. Last modification occurred on 10/17/2016 1:12:45 PM. In Vivo Communication and Mass Media - ... method for analysis of Gallic acid gallic acid Subject Category: ... methanol: formic acid (3: 3: 0.2: 0.8 v/v) system was developed as a mobile phase. Recovery was 99.37 % and 98.68% for ascorbic and gallic acid, respectively and the coefficient of variance ⦠Reference data were obtained primarily from the PubChem database.. Three dimensional molecular rendering uses Jmol.. InChI string and atom numbering calculated using ALATIS (Hesam Dashti, William M. Westler, John L. Markley, Hamid R. Eghbalnia, "Unique identifiers for small molecules enable rigorous labeling of ⦠5995-86-8. The full spectrum can only be viewed ⦠Gallic acid is an antioxidant which can inhibit both COX-2[1]. 50 μl volumes of ⦠View the Full Spectrum for FREE! The SE-fraction contained gallic acid and ellagic acid. Gallic acid monohydrate View entire compound with free spectra: 2 NMR, and 3 FTIR ... 188.135 g/mol: Molecular Formula: C7H8O6: Exact Mass: 188.032088 g/mol: 13C Nuclear Magnetic Resonance (NMR) Chemical Shifts. Limits of detection were 1.42 and 1.56 μg mL-1 and limits of quantification were 4.32 and 4.73 μg mL-1 for ascorbic and gallic acid, respectively. It is a white solid, although samples are typically brown owing to partial oxidation. The results indicate that ellagic acid, gallic acid and punicalagin may be the compounds responsible for the anti-inflammatory potential of P. granatum. Gallic acid (also known as 3,4,5-trihydroxybenzoic acid) is a trihydroxybenzoic acid with the formula C 6 H 2 3 CO 2 H. It is classified as a phenolic acid.It is found in gallnuts, sumac, witch hazel, tea leaves, oak bark, and other plants. ... Mass spectrum showing the presence of ellagic acid [M-H] -m/z 301. Structure, properties, spectra, suppliers and links for: Gallic acid, 149-91-7. 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