Search results
Results from the WOW.Com Content Network
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 2 H 3 O − 2.
Ethyl acetate (systematically ethyl ethanoate, commonly abbreviated EtOAc, ETAC or EA) is the organic compound with the formula CH 3 CO 2 CH 2 CH 3, simplified to C 4 H 8 O 2.This flammable, colorless liquid has a characteristic sweet smell (similar to pear drops) and is used in glues, nail polish removers, and the decaffeination process of tea and coffee.
Uranyl acetate is the acetate salt of uranium oxide, a toxic yellow-green powder useful in certain laboratory tests. Structurally, it is a coordination polymer with formula UO 2 (CH 3 CO 2 ) 2 (H 2 O)·H 2 O.
Potassium acetate (as a substitute for calcium chloride or magnesium chloride) can be used as a deicer to remove ice or prevent its formation. It offers the advantage of being less aggressive on soils and much less corrosive: [5] for this reason, it is preferred for airport runways although it is more expensive.
Aluminium acetate or aluminium ethanoate [1] (also "aluminum ~"), sometimes abbreviated AlAc in geochemistry, [2] can refer to a number of different salts of aluminium with acetic acid. In the solid state, three salts exist under this name: basic aluminium monoacetate , (HO) 2 AlCH 3 CO 2 , basic aluminium diacetate , HOAl(CH 3 CO 2 ) 2 , [ 3 ...
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.
Octyl acetate, or octyl ethanoate, is an organic compound with the formula CH 3 (CH 2) 7 O 2 CCH 3. It is classified as an ester that is formed from 1-octanol (octyl alcohol) and acetic acid. It is found in oranges, grapefruits, and other citrus products. [10] Octyl acetate can be synthesized by the Fischer esterification of 1-octanol and ...
Polyvinyl acetate is also the raw material to make other polymers like: Polyvinyl alcohol −[HOCHCH 2 ]−: Polyvinyl acetate is partially or completely hydrolysed to give polyvinyl alcohol. This reversible saponification and esterification reaction was a strong hint for Hermann Staudinger in the formulation of his theory of macromolecules .