Section 3: Hazards Identification Potential Acute Health Effects: Slightly hazardous in case of skin contact (irritant), of eye contact (irritant), of ingestion, of inhalation. The ⦠5 / 14. Cinnamic Acid C9H8O2 Molar Mass, Molecular Weight. Synthesis of the Department of trans isomers. Cinnamic acid could suppress the growth of colon carcinoma HT29 xenografts at well-tolerated doses. The polycondensates of isophthalic acid-cinnamic acid-glycerine system were synthesized. Warning. You can also browse global suppliers,vendor,prices,Price,manufacturers of trans-Cinnamic acid(140-10-3). The molecular weight of urea is 60.16 g/mol and the molecular weight of cinnamic acid is 148.16 g/mol. trans-CINNAMIC ACID, ETHYL ESTER View entire compound with free spectra: 4 NMR and 2 FTIR. Converts 3-phenylpropionate-dihydrodiol (PP-dihydrodiol) and cinnamic acid-dihydrodiol (CI-dihydrodiol) into 3-(2,3-dihydroxylphenyl)propanoic acid (DHPP) and 2,3-dihydroxicinnamic acid (DHCI), respectively. 1.Cinnamic acid flavor:used as Fixed sweet agent in Beverages, cold drinks, candy, alcohol . 66 ⦠1.2475g/cm 3 density (4 ° C). 190 °C TCI M0576: 173.5 °C (Literature) Indofine [01-1015] 171-175 °C Alfa Aesar: 171-173 °C Manchester Organics N20237: 174 °C Jean-Claude Bradley Open Melting Point Dataset 12335: 173 °C Jean-Claude Bradley Open Melting Point Dataset 8580: 170-173 °C Alfa Aesar H60144: 171-175 °C Alfa Aesar A13870: 171-173 °C ⦠This compound exhibited a molecular weight of a positively ionised mass of m/z = 161.0962 [M+H] +, when tCA was used, and of m/z = 168.1406 [M+H] + when D 7-tCA was used. Cinnamic-acid (CA) content (mol%) â a â a â c: 6.8: Weight-average molecular weight (w) â b: 35 °C: 198 000: 217 000: Polydispersity index (w / n) â b: 35 °C: 3.3: 3.6: Mechanical: Charpy notched impact strength (kJ m â2) ISO 179-1: 23 ± 2 °C, 2 mm min â1: 5.3: 7.8: Young's modulus (MPa) ISO 527: 23 ± 2 °C, 2 mm min ⦠16 / 106. The structure, molecular formula, solubility, and molecular weight of cinnamaldehyde, cinnamic acid, citric acid, and levulinic acid Compound Structure Molecular Formula Molecular Weight (Da) Solubility (M) Citric acid Levulinic acid C 6 H 8 O 7 192.12 4.809 M in water Cinnamic acid C 5 H 8 O 3 116.11 6.746 M in ⦠2.Cinnamic acid has a strong sterilization, anti-corrosion effect as food. View the Full Spectrum for FREE! The molecular weights of these products were determined by two methods, viscosity method and osmotic pressure methods. After the addition of bromine to trans-cinnamic acid, the product was identified by its melting point and infrared spectrum resulting in erythro-2,3-Dibromo-3-phenylpropanoic acid after ⦠Cinnamic acid is a white crystalline organic acid, which is slightly soluble in water. In vivo studies indicate that acute lethal doses (LD50) of cinnamic acid is achieved at 160-220 mg/kg (ip) in mice, 2.5 g/kg (oral) in rats and 5 g/kg (dermal) in rabbits. Dilution Calculator. Potential Chronic Health Effects: ⦠Other names: Sinapinic acid; Sinapic acid; trans-3,5-Dimethoxy-4-hydroxycinnamic acid; 2-Propenoic acid, 3-(4-hydroxy-3,5-dimethoxyphenyl)-; Cinnamic acid, 4-hydroxy-3,5-dimethoxy-; 4-Hydroxy-3,5-dimethoxycinnamic acid Permanent link for this species. Trans-Cinnamic Acid Molecular weight 148.161 g/mol, Solid, Melting point 133 °C, White. Name CAS # % by Weight {trans-}Cinnamic acid 140-10-3 100 Toxicological Data on Ingredients: Not applicable. p-Coumaric acid is a hydroxycinnamic acid, an organic compound that is a hydroxy derivative of cinnamic acid.There are three isomers of coumaric acidâo-coumaric acid, m-coumaric acid, and p-coumaric acidâthat differ by the position of the hydroxy substitution of the phenyl group. Trans-cinnamic acid (E-3-phenyl-2-propanoic acid) has a molecular weight of 148 g/mol and a melting point of 133 degrees Celsius. Cells are grown for 3 days at 37°C in the presence or absence of the drug, then detached with trypsin/EDTA and counted in a Coulter counter. trans-Cinnamic acid analytical standard provided with w/w absolute assay, to be used for quantitative titration. H315 H319 H335. Our previous work with in vivo experiments already proved that UP1 was derived by conversion of tCA (Gottardi et al. At last,trans-Cinnamic acid⦠3.3).The shikimate pathway provides an ⦠The most plant phenolics are derived from trans-cinnamic acid, which is formed from l-phenylalanine by the action of l-phenylalanine ammonia-lyase (PAL), the branch point enzyme between primary (shikimate pathway) and secondary (phenyl propanoid pathway) metabolism (Fig. There are several enantiomers of 2,3-dibromo-3-phenylpropanoic acid, they all have a molecular weight of 308 g/mol (Molecular Weight: 307.96662 to be specific).The (2R, 3S) and (2S, 3R) have a ⦠View the Full Spectrum for FREE! Use this link for bookmarking this species for future reference. 133 ° C melting point. Briefly, 5 X10 4 cells are plated in each well of a 24-well plate, allowed to attach overnight, and treated with compounds (e.g., Cinnamic acid: 2.5, 5, 10, 20, 30 mM) the following day. trans-cinnamic acid shows moderate inhibition on the rainbow trout intestinal isolates A. sobria SY-AS3 and S. baltica, SY-S145, gill isolate F. spartansii SY-FS1 and fish pathogens A. ⦠The boiling point of 300 ° C. Soluble in the ether, benzene, acetone, acetic acid, carbon disulfide, oils, can be dissolved in ethanol, methanol, ⦠ChemicalBook Providetrans-Cinnamic acid(140-10-3) 1H NMR,IR2,MS,IR3,IR1,1H NMR,Raman,ESR,13C NMR,Spectrum trans-Cinnamic acid is an antimicrobial activity, with minimal inhibitory concentration (MIC) of 250 μg/mL against fish pathogen A. sobria, SY-AS1. ⦠Chlorogenic acid can be isolated from green coffee beans, and forms a black compound with iron, believed to be responsible for the blackening of ⦠In the synthesis of resin, the reaction temperature was kept at 232
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