Chemistry:Tert-Butyl acetate
From HandWiki
Names | |
---|---|
Preferred IUPAC name
tert-Butyl acetate | |
Other names
| |
Identifiers | |
3D model (JSmol)
|
|
ChemSpider | |
PubChem CID
|
|
UNII | |
| |
| |
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 | |
Main hazards | 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)
|
TWA 200 ppm (950 mg/m3)[2] |
REL (Recommended)
|
TWA 200 ppm (950 mg/m3)[2] |
IDLH (Immediate danger)
|
1500 ppm[2] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
Tracking categories (test):
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
References
- ↑ 1.0 1.1 1.2 1.3 tert-Butyl acetate (11th ed.). p. 236.
- ↑ 2.0 2.1 2.2 2.3 2.4 NIOSH Pocket Guide to Chemical Hazards. "#0074". National Institute for Occupational Safety and Health (NIOSH). https://www.cdc.gov/niosh/npg/npgd0074.html.
- ↑ "Update: U.S. EPA Exempt Volatile Organic Compounds" (in en-US). 2018-01-30. https://www.paint.org/voc-exempt/.
External links
Original source: https://en.wikipedia.org/wiki/Tert-Butyl acetate.
Read more |