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sec-Butyl acetate, or s-butyl acetate, is an ester commonly used as a solvent in lacquers and enamels, where it is used in the production of acyclic polymers, vinyl resins, and nitrocellulose. [3] It is a clear flammable liquid with a sweet smell.
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.
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 ...
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Skeletal formula of butyl (here connected to an R group) Common name Preferred IUPAC name Alternate notation Fully systematic name Symbol; n-butyl butyl butyl butan-1-yl Bu, n-Bu, nBu, n Bu sec-butyl butan-2-yl 1-methylpropyl butan-2-yl s-Bu, sBu, s Bu isobutyl, iso-butyl 2-methylpropyl 2-methylpropyl 2-methylpropan-1-yl i-Bu, iBu, i Bu tert ...
An ester of carboxylic acid.R stands for any group (organic or inorganic) and R′ stands for organyl group.. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (−R).
The molecular formula C 7 H 14 O 2 may refer to: Amyl acetate; sec-Amyl acetate; n-Butyl glycidyl ether; Butyl propionate. n-Butyl propionate; sec-Butyl propionate; Isobutyl propionate; tert-Butyl propionate; Ethyl isovalerate; Ethyl pentanoate; Heptanoic acid; Isoamyl acetate; Methyl hexanoate
Alkyl groups that contain one ring have the formula −C n H 2n−1, e.g. cyclopropyl and cyclohexyl. The formula of alkyl radicals are the same as alkyl groups, except the free valence " − " is replaced by the dot "•" and adding "radical" to the name of the alkyl group (e.g. methyl radical •CH 3 ).