WebNov 14, 2012 · chloroacetic acid (50%; mass/vol) 116.48: 3.0 g (6 mL 50% - m/v) 25.8: 170--- msds: KOH (pellets) 56.11: 4.0 g: 71.3: 380--- msds: HCl (12 M; 12 mmol/mL) … WebChloroacetic acid (CAA, monochloroacetic acid, MCAA) is a halogenated aliphatic carboxylic acid generally used as herbicide and preservative. Its mutagenic effects have been studied in Rattus norvegicus. [ 1] The rate of degradation of MCA by photocatalysis using TiO 2 at pH3 is reported to be enhanced under the influence of ozone. [ 2]
What is the melting point of dichloroacetic acid?
Chloroacetic acid was first prepared (in impure form) by the French chemist Félix LeBlanc (1813–1886) in 1843 by chlorinating acetic acid in the presence of sunlight, and in 1857 (in pure form) by the German chemist Reinhold Hoffmann (1831–1919) by refluxing glacial acetic acid in the presence of chlorine and sunlight, and then by the French chemist Charles Adolphe Wurtz by hydrolysis of chloroacetyl chloride (ClCH2COCl), also in 1857. WebMelting point. 60-63° Boiling Point. 189° ... Applications. Chloroacetic acid is used in the production of pharmaceuticals, dyes, detergents, synthetic caffeine, glycine and thioglycolic acid, which acts as a stabilizer in PVC. It acts as a precursor to glyphosate and adrenaline. It also serves as a preservative and bacteriostat. deere credit union ottumwa
Tables of Unknowns and Derivatives
WebChloroacetic acid: Molecular weight of C 2 H 3 O 2 Cl: 94.49 g/mol: Density of Chloroacetic acid: 1.58 g/cm 3: Boiling point of Chloroacetic acid: 189.3 °C: Melting point of Chloroacetic acid: 63 °C http://site.iugaza.edu.ps/rmorjan/files/2010/02/41669_App_p357-366.pdf WebIt is prepared by the reaction of chlorine with acetic acid in the presence of a suitable catalyst such as red phosphorus. This reaction is Hell–Volhard–Zelinsky halogenation . CH 3COOH + 3 Cl 2 → CCl 3COOH + 3 HCl Another route to trichloroacetic acid is the oxidation of trichloroacetaldehyde. Use [ edit] fedex rolling meadows