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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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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]
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 ...
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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.