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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 2 H 3 O − 2.
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Acetoacetic acid (IUPAC name: 3-oxobutanoic acid, also known as acetonecarboxylic acid or diacetic acid) is the organic compound with the formula CH 3 COCH 2 COOH. It is the simplest beta-keto acid, and like other members of this class, it is unstable.
In chemistry, acetylation is an organic esterification reaction with acetic acid. It introduces an acetyl group into a chemical compound. Such compounds are termed acetate esters or simply acetates. Deacetylation is the opposite reaction, the removal of an acetyl group from a chemical compound.
The suffix-oate is the IUPAC nomenclature used in organic chemistry to form names of compounds formed with ester. They are of two types: They are of two types: Formed by replacing the hydrogen atom in the –COOH by some other radical , usually an alkyl or aryl radical forming an ester .
Propylene glycol methyl ether acetate (PGMEA, 1-methoxy-2-propanol acetate) is a P-type glycol ether used in inks, coatings, and cleaners. It is sold by Dow Chemical under the name Dowanol PMA, [ 3 ] by Shell Chemical under the name methyl proxitol acetate, [ 4 ] [ 5 ] and by Eastman under the name PM Acetate.
Amyl acetate (pentyl acetate) is an organic compound and an ester with the chemical formula CH 3 COO[CH 2] 4 CH 3 and the molecular weight 130.19 g/mol. It is colorless and has a scent similar to bananas [3] [4] and apples. [5] The compound is the condensation product of acetic acid and 1-pentanol.
Potassium acetate (also called potassium ethanoate), (CH 3 COOK) is the potassium salt of acetic acid. It is a hygroscopic solid at room temperature. Preparation