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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.
Products such as calcium acetate, sodium acetate, acetic acid, and acetic anhydride became the basis for the company’s platforms. During World War II, RDX, a powerful explosive, was manufactured for the U.S. government at Holston Ordnance Works at Tennessee Eastman sites. At the peak of production near the end of the war, the ordnance plant ...
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]
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 trichloroacetate is a chemical compound with a formula of CCl 3 CO 2 Na. It is used to increase sensitivity and precision during transcript mapping. [1] It was previously used as an herbicide starting in the 1950s but regulators removed it from the market in the late 1980s and early 1990s. [2] [3] [4] [5]
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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.