- Butyl acetate
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n-Butyl acetate Butyl ethanoateOther namesButyl acetate
Acetic acid, n-butyl ester
ButileIdentifiers CAS number 123-86-4 PubChem 31272 ChemSpider 29012 UNII 464P5N1905 KEGG C12304 ChEBI CHEBI:31328 ChEMBL CHEMBL284391 Jmol-3D images Image 1 - CCCCOC(=O)C
Properties Molecular formula C6H12O2 Molar mass 116.16 g/mol Appearance Colourless liquid with fruity odor Density 0.88 g/cm3, liquid Melting point -74 °C (199 K, -101°F)
Boiling point 126 °C (399 K, 256°F)
Solubility in water 0.7 g/100 ml (20.0 °C) Refractive index (nD) 1.394 (20.0 °C) Hazards Main hazards Flammable Flash point 24 °C (297 K) Related compounds Related acetates propyl acetate
amyl acetateRelated compounds butanol acetate (verify) (what is: / ?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)Infobox references For other uses, see Butyl acetate (disambiguation).n-Butyl acetate, also known as butyl ethanoate, is an organic compound commonly used as a solvent in the production of lacquers and other products. It is also used as a synthetic fruit flavoring in foods such as candy, ice cream, cheeses, and baked goods. Butyl acetate is found in many types of fruit, where along with other chemicals it imparts characteristic flavors. It is a colourless flammable liquid with a sweet smell of banana.
The other three isomers of butyl acetate are: isobutyl acetate, tert-butyl acetate, and sec-butyl acetate.
Contents
Production
Butyl acetates are commonly manufactured by the Fischer esterification of a butanol isomer and acetic acid with the presence of catalytic sulfuric acid under reflux conditions. [1]
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.
References
- ^ Acetic acid. (2003). In Ullman's encyclopedia of industrial chemistry (6th ed., Vol. 1, pp. 170-171). Weinheim, Germany: Wiley-VCH.
External links
Categories:- Ester solvents
- Flavors
- Acetate esters
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