Names | |
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Preferred IUPAC name
Butan-2-yl acetate
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Other names
2-Butyl acetate
sec-Butyl acetate (no longer recommended) sec-Butyl ester; s-Butyl acetate; sec-Butyl ester of acetic acid 1-Methylpropyl acetate |
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Identifiers | |
3D model (Jmol)
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ChemSpider | |
ECHA InfoCard | 100.003.001 |
PubChem CID
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UNII | |
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Properties | |
C6H12O2 | |
Molar mass | 116.16 g/mol |
Appearance | clear, liquid |
Odor | fruity |
Density | 0.87 g/cm3, liquid |
Melting point | −99 °C (−146 °F; 174 K) |
Boiling point | 112 °C (234 °F; 385 K) |
0.80 g/100 mL | |
Vapor pressure | 10 mmHg |
Hazards | |
Main hazards | Flammable |
Safety data sheet | External MSDS |
Flash point | 17 °C; 62 °F; 290 K |
Explosive limits | 1.7%-9.8% |
US health exposure limits (NIOSH): | |
PEL (Permissible)
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TWA 200 ppm (950 mg/m3) |
REL (Recommended)
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TWA 200 ppm (950 mg/m3) |
IDLH (Immediate danger)
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1700 ppm |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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what is ?) | (|
Infobox references | |
sec-Butyl acetate, or s-butyl acetate, is a solvent commonly used as a solvent in lacquers and enamels, where it is used in the production of acyclic polymers, vinyl resins, and nitrocellulose. It is a clear flammable liquid with a sweet smell.
sec-Butyl acetate has three isomers that are also acetate esters: n-butyl acetate, isobutyl acetate, and tert-butyl acetate.
The first method of production of sec-butyl acetate was the esterification of sec-butanol and acetic anhydride It was experimentally determined and published in 1946 by Rolf Altschul.
The LD50 for rats is 13 g/kg. Exposure in humans to significant quantities of sec-butyl acetate can cause irritation to the eyes, mouth, throat, nose, and skin. Ingestion and inhalation of sec-butyl acetate can cause central nervous system depression producing symptoms of dizziness and disorientation.