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A supersaturated solution of sodium acetate in water is supplied with a device to initiate crystallization, a process that releases substantial heat. Solubility from CRC Handbook. Sodium acetate trihydrate crystals melt at 58–58.4 °C (136.4–137.1 °F), [12] [13] and the liquid sodium acetate dissolves in the released water of crystallization.
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The acetate anion, [CH 3 COO] −,(or [C 2 H 3 O 2] −) is one of the carboxylate family. It is the conjugate base of acetic acid. Above a pH of 5.5, acetic acid converts to acetate: [1] CH 3 COOH ⇌ CH 3 COO − + H + Many acetate salts are ionic, indicated by their tendency to dissolve well in water.
NaC 3 H 6 NO 3: sodium hydromethylglycinate: 70161–44–3 NaC 4 H 7 O 4: sodium diacetate: 126–96–5 NaC 6 H 6 SO 3: sodium benzosulfonate: 515–42–4 NaC 7 H 5 O 2: sodium benzoate: 532–32–1 NaC 7 H 8 SO 3: sodium tosylate: 657–84–1 NaC 8 H 7 O 2: sodium phenylacetate: 114–70–5 NaC 8 H 9 SO 3: sodium xylenesulfonate: 1300 ...
Sodium chloroacetate is the organic compound with the formula CH 2 ClCO 2 Na. A white, water-soluble solid, it is the sodium salt of chloroacetic acid. Many of its uses are similar to those of the parent acid. It is prepared by treating chloroacetic acid with sodium carbonate. [1] [2]
Ethyl diazoacetate (N=N=CHC(O)OC 2 H 5) is a diazo compound and a reagent in organic chemistry.It was discovered by Theodor Curtius in 1883. [4] The compound can be prepared by reaction of the ethyl ester of glycine with sodium nitrite and sodium acetate in water.
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Reaction of the sodium cyanoacetate with ethyl bromide in an aqueous–organic two-phase system in the presence of a phase transfer catalyst. [ 4 ] Oxidation of 3-ethoxypropionitrile, an ether , with oxygen under pressure in the presence of cobalt(II) acetate tetrahydrate as catalyst and N -hydroxyphthalimide as a radical generator.