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Names | |
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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 |
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KEGG | |
PubChem CID | |
RTECS number |
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UNII | |
UN number | 1123 |
CompTox Dashboard (EPA) | |
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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 |
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Refractive index (nD) | 1.3941 (20 °C) [1] |
Viscosity |
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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: | |
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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.