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An acetate is a salt formed by the combination of acetic acid with a base (e.g. alkaline, earthy, metallic, nonmetallic or radical base). "Acetate" also describes the conjugate base or ion (specifically, the negatively charged ion called an anion) typically found in aqueous solution and written with the chemical formula C
acetate ion: 71-50-1 CH 3 COOCHCH 2: vinyl acetate: 108-05-4 CH 3 COOCH 2 C 6 H 5: benzyl acetate: 140-11-4 CH 3 COO(CH 2) 2 CH(CH 3) 2: isoamyl acetate: 123-92-2 CH 3 COOH: acetic acid ethanoic acid: 64-19-7 CH 3 COONa: sodium acetate: 127-09-3 CH 3 COOK: potassium acetate: 127-08-2 CH 3 COORb: rubidium acetate: 563-67-7 CH 3 COOCs: caesium ...
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.
The conversion of methyl acetate back into its components, by an acid, is a first-order reaction with respect to the ester. The reaction of methyl acetate and a base, for example sodium hydroxide, is a second-order reaction with respect to both reactants. Methyl acetate is a Lewis base that forms 1:1 adducts with a variety of Lewis acids.
n-Butyl acetate is an organic compound with the formula CH 3 CO 2 (CH 2) 3 CH 3. A colorless, flammable liquid, it is the ester derived from n- butanol and acetic acid . It is found in many types of fruit, where it imparts characteristic flavors and has a sweet smell of banana or apple.
Copper(I) acetate (cuprous acetate) is an organic copper salt of acetic acid with chemical formula CH 3 COOCu. Under standard conditions, copper(I) acetate is a colorless, odorless crystal. Chemical propieties
The molecular formula C 6 H 12 O 2 (Molar mass: 116.15 g/mol) may refer to: Carboxylic acids with formula C 6 H 12 O 2: Hexanoic acid; 4-Methylpentanoic acid; Esters with formula C 6 H 12 O 2: Butyl acetate; sec-Butyl acetate; tert-Butyl acetate; Ethyl butyrate; Isobutyl acetate; Isoamyl formate; Methyl pentanoate; Methyl pivalate; Propyl ...
It is not well known and was discovered accidentally by an attempt trying to make boron triacetate in the 1950s. It was made by reacting boric acid and acetic anhydride around 75 °C (167 °F) under nitrogen which created tetraacetyl diborate and acetic acid.