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Butyl acetate

chemical compound

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Record originEnglish Wikipedia
Text licenseCC BY-SA 4.0
Source revisionJun 17, 2026
Entity authorityQ411073
Source-derived summary

n-Butyl acetate is an organic compound with the formula CH3CO2(CH2)3CH3. 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. It is used as an industrial solvent.

The other three isomers (four, including stereoisomers) of butyl acetate are isobutyl acetate, tert-butyl acetate, and sec-butyl acetate (two enantiomers).

Production and use

Butyl acetate is commonly manufactured by the Fischer esterification of n-butanol and acetic acid with the presence of sulfuric acid:

Butyl acetate is mainly used as a solvent for coatings and inks. It is a component of fingernail polish.

Occurrence in nature

Apples, especially of the "Red Delicious" variety, are flavored in part by this chemical. The alarm pheromones emitted by the Koschevnikov gland of honey bees contain butyl acetate.

Editorial summary

The public source identifies “Butyl acetate” as chemical compound. This brief keeps that definition visible, then builds a research path around Butyl, acetate and chemical.

Editorial reviewA practical orientation to terminology and classification, particularly when read beside dated observations, specimens or technical literature. The current 146-word lead offers orientation but no explicit four-digit date, so chronology should not be assumed. The selected authority fields contribute no independent date. Its value is orientation rather than verdict, with Butyl, acetate and chemical providing the first useful test.
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Why this record matters

A short description can identify a subject without explaining its stakes. For “Butyl acetate”, the useful work is to connect “chemical compound” to the records capable of establishing context and consequence.

Evidence profile

Stable identifiers, scientific names and standards terminology offer the best bridge between this overview and specialist evidence. The source revision retrieved here is dated Jun 17, 2026. The linked authority identifier is Q411073. None of the 0 selected statements returned an explicit reference.

Critical limits

Scientific names, classifications and consensus can change while older terminology persists in catalogues and historical literature. The lead is largely declarative, so disagreement and counter-evidence require a deliberate search beyond the opening account. Authority statements aid reconciliation but still require their own references, qualifiers and ranks to be checked.

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  2. Expand the search: follow Butyl acetate primary sources, Butyl acetate archive and Butyl research across catalogues and specialist indexes.
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Source & attribution

This entry incorporates text from Butyl acetate” on English Wikipedia. Contributors are listed in the page history. Text is available under the Creative Commons Attribution-ShareAlike 4.0 License. Selected authority identifiers and statements are retrieved from Wikidata under CC0; their references and qualifiers remain part of the verification path.