|   | |
|   | |
| Names | |
|---|---|
| Preferred IUPAC name Butyl acetate | |
| Systematic IUPAC name Butyl ethanoate | |
| Other names n-Butyl acetate Acetic acid n-butyl ester Butile | |
| Identifiers | |
| 3D model (JSmol) | |
| Abbreviations | BuAcO | 
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.004.236 | 
| EC Number | 
 | 
| KEGG | |
|  PubChem CID | |
| RTECS number | 
 | 
| UNII | |
| UN number | 1123 | 
|  CompTox Dashboard (EPA) | |
| 
 | |
| 
 | |
| Properties | |
| CH3CO2(CH2)3CH3 | |
| Molar mass | 116.160 g·mol−1 | 
| Appearance | Colorless liquid | 
| Odor | Fruity | 
| Density | 0.8825 g/cm3 (20 °C) [1] | 
| Melting point | −78 °C (−108 °F; 195 K) [1] | 
| Boiling point | 126.1 °C (259.0 °F; 399.2 K) at 760 mmHg [1] | 
| 0.68 g/100 mL (20 °C) [1] | |
| Solubility | Miscible in EtOH Soluble in acetone, CHCl3 [1] | 
| log P | 1.82 [1] | 
| Vapor pressure | |
|  Henry's law constant (kH) | 0.281 L·atm/mol | 
| −77.47·10−6 cm3/mol | |
| Thermal conductivity | 
 | 
|  Refractive index (nD) | 1.3941 (20 °C) [1] | 
| Viscosity | 
 | 
| Structure | |
| 1.87 D (24 °C) [1] | |
| Thermochemistry | |
|  Heat capacity (C) | 225.11 J/mol·K [2] | 
|  Std enthalpy of formation (ΔfH⦵298) | −609.6 kJ/mol [2] | 
|  Std enthalpy of combustion (ΔcH⦵298) | 3467 kJ/mol [2] | 
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
| Main hazards | Flammable | 
| GHS labelling: | |
|    [3] | |
| Warning | |
| H226, H336 [3] | |
| P261 [3] | |
| NFPA 704 (fire diamond) | |
| Flash point | 22 °C (72 °F; 295 K) [4] | 
| 370 °C (698 °F; 643 K) [4] | |
|  Threshold limit value (TLV) | 150 ppm [1] (TWA), 200 ppm [1] (STEL) | 
| Lethal dose or concentration (LD, LC): | |
| LD50 (median dose) | 10768 mg/kg (~10.8g/kg) (rats, oral) [4] | 
| LC50 (median concentration) | 160 ppm (rat, 4 hr) 2000 ppm (rat, 4 hr) 391 ppm (rat, 4 hr) 1242 ppm (mouse, 2 hr) [5] | 
| LCLo (lowest published) | 14,079 ppm (cat, 72 min) 13,872 ppm (guinea pig, 4 hr) [5] | 
| NIOSH (US health exposure limits): | |
|  PEL (Permissible) | TWA 150 ppm (710 mg/m3) [4] | 
|  REL (Recommended) | TWA 150 ppm (710 mg/m3) ST 200 ppm (950 mg/m3) [6] | 
|  IDLH (Immediate danger) | 1700 ppm [6] | 
| Related compounds | |
| Related acetates  | Ethyl acetate Propyl acetate Amyl acetate | 
| Related compounds | Butanol | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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. [7]
The other three isomers (four, including stereoisomers) of butyl acetate are isobutyl acetate, tert-butyl acetate, and sec-butyl acetate (two enantiomers).
Butyl acetate is commonly manufactured by the Fischer esterification of butanol and acetic acid with the presence of sulfuric acid: [7]
 
 Butyl acetate is mainly used as a solvent for coatings and inks. [7] It is a component of fingernail polish. [8]
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.