Isobutyl acetate
![]() |
|
![]() |
|
Names | |
---|---|
IUPAC name
2-methylpropyl acetate
|
|
Other names
Isobutyl ester
|
|
Identifiers | |
110-19-0 ![]() |
|
ChEBI | CHEBI:50569 ![]() |
ChEMBL | ChEMBL46999 ![]() |
ChemSpider | 7747 ![]() |
Jmol 3D model | Interactive image |
PubChem | 8038 |
UNII | 7CR47FO6LF ![]() |
|
|
|
|
Properties | |
C6H12O2 | |
Molar mass | 116.16 g/mol |
Appearance | Colourless liquid |
Odor | Fruity, floral[3] |
Density | 0.875 g/cm3, liquid |
Melting point | −99 °C (−146 °F; 174 K) |
Boiling point | 118 °C (244 °F; 391 K) |
Slightly soluble 0.63-0.7g/100g at 20 °C |
|
Vapor pressure | 13 mmHg (20°C)[3] |
Vapor pressure | {{{value}}} |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
|
![]() ![]() ![]() |
|
Infobox references | |
The chemical compound isobutyl acetate, also known as 2-methylpropyl ethanoate (IUPAC name) or β-methylpropyl acetate, is a common solvent. It is produced from the esterification of isobutanol with acetic acid. It is used as a solvent for lacquer and nitrocellulose. Like many esters it has a fruity or floral smell at low concentrations and occurs naturally in raspberries, pears and other plants. At higher concentrations the odor can be unpleasant and may cause symptoms of central nervous system depression such as nausea, dizziness and headache.
A common method for preparing isobutyl acetate is Fischer esterification, where precursors isobutyl alcohol and acetic acid are heated in the presence of a strong acid.
Isobutyl acetate has three isomers: n-butyl acetate, tert-butyl acetate, and sec-butyl acetate, which are also common solvents.
References
<templatestyles src="Reflist/styles.css" />
Cite error: Invalid <references>
tag; parameter "group" is allowed only.
<references />
, or <references group="..." />
- ↑ Isobutyl acetate Chemical Profile, Canadian Centre for Occupational Health and Safety
- ↑ Isobutyl acetate at chemicalland21.com
- ↑ 3.0 3.1 Lua error in package.lua at line 80: module 'strict' not found.