tert-Butyl acetate
(Redirected from Tert-butyl acetate)
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| Names | |
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| Preferred IUPAC name
tert-Butyl acetate | |
Other names
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| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
| ECHA InfoCard | 100.007.965 |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C6H12O2 | |
| Molar mass | 116.160 g·mol−1 |
| Appearance | Colorless liquid |
| Odor | Fruity |
| Density | 0.8593 g/cm3[1] |
| Boiling point | 97.8 °C (208.0 °F; 370.9 K)[1] |
| 0.8 wt% at 22 °C | |
| Solubility in ether and ethanol | Miscible[1] |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards
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Flammable |
| Flash point | 22 °C; 72 °F; 295 K[2] |
| Explosive limits | From 1.5% to unknown[2] |
| NIOSH (US health exposure limits): | |
PEL (Permissible)
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TWA 200 ppm (950 mg/m3)[2] |
REL (Recommended)
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TWA 200 ppm (950 mg/m3)[2] |
IDLH (Immediate danger)
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1500 ppm[2] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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tert-Butyl acetate, t-butyl acetate or TBAc is a colorless flammable liquid with a camphor- or blueberry-like smell. It is used as a solvent in the production of lacquers, enamels, inks, adhesives, thinners and industrial cleaners. It has recently gained EPA volatile organic compound (VOC) exempt status.[3]
It is manufactured from acetic acid and isobutylene.[1] An attempt at Fischer esterification would lead to elimination of tert-butyl alcohol to isobutylene.
Butyl acetate has four isomers (or five, including stereoisomers): tert-butyl acetate, n-butyl acetate, isobutyl acetate, and sec-butyl acetate (two enantiomers).
See also
[edit]References
[edit]- ^ a b c d tert-Butyl acetate (11th ed.). p. 236.
{{cite book}}:|work=ignored (help) - ^ a b c d e NIOSH Pocket Guide to Chemical Hazards. "#0074". National Institute for Occupational Safety and Health (NIOSH).
- ^ "Update: U.S. EPA Exempt Volatile Organic Compounds". American Coatings Association. 2018-01-30. Retrieved 2019-03-20.